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Title: The Geographical Distribution of Animals, Volume 1 Author: Alfred Russel Wallace Release date: February 6, 2018 [eBook #56506] Language: English Credits: Produced by MWS and the Online Distributed Proofreading Team at http://www.pgdp.net (This file was produced from images generously made available by The Internet Archive) *** START OF THE PROJECT GUTENBERG EBOOK THE GEOGRAPHICAL DISTRIBUTION OF ANIMALS, VOLUME 1 *** Produced by MWS and the Online Distributed Proofreading Team at http://www.pgdp.net (This file was produced from images generously made available by The Internet Archive) Transcriber's note: The Errata (after the List of Plates) have been worked into the main text. All other apparent mistakes have been retained as printed. Text enclosed by underscores is in italics (_italics_); page numbers enclosed by curly braces (example: {25}) have been incorporated to facilitate the use of the Index.. * * * * * [Illustration: Zoogeographical Regions] THE GEOGRAPHICAL DISTRIBUTION OF ANIMALS _WITH A STUDY OF THE RELATIONS OF LIVING AND EXTINCT FAUNAS AS ELUCIDATING THE PAST CHANGES OF THE EARTH'S SURFACE._ BY ALFRED RUSSEL WALLACE, AUTHOR OF "THE MALAY ARCHIPELAGO," ETC. WITH MAPS AND ILLUSTRATIONS. _IN TWO VOLUMES.--VOLUME I._ London: MACMILLAN AND CO. 1876. [_The Right of Translation and Reproduction is Reserved._] LONDON: R. CLAY, SONS, AND TAYLOR, PRINTERS, BREAD STREET HILL. PREFACE. The present work is an attempt to collect and summarize the existing information on the Distribution of Land Animals; and to explain the more remarkable and interesting of the facts, by means of established laws of physical and organic change. The main idea, which is here worked out in some detail for the whole earth, was stated sixteen years ago in the concluding pages of a paper on the "Zoological Geography of the Malay Archipelago," which appeared in the _Journal of Proceedings of the Linnean Society_ for 1860; and again, in a paper read before the Royal Geographical Society in 1863, it was briefly summarized in the following passage:-- "My object has been to show the important bearing of researches into the natural history of every part of the world, upon the study of its past history. An accurate knowledge of any groups of birds or of insects and of their geographical distribution, may enable us to map out the islands and continents of a former epoch,--the amount of difference that exists between the animals of adjacent districts being closely related to preceding geological changes. By the collection of such minute facts, alone, can we hope to fill up a great gap in the past history of the earth as revealed by geology, and obtain some indications of the existence of those ancient lands which now lie buried beneath the ocean, and have left us nothing but these living records of their former existence." The detailed study of several groups of the birds and insects collected by myself in the East, brought prominently before me some of the curious problems of Geographical Distribution; but I should hardly have ventured to treat the whole subject, had it not been for the kind encouragement of Mr. Darwin and Professor Newton, who, about six years ago, both suggested that I should undertake the task. I accordingly set to work; but soon became discouraged by the great dearth of materials in many groups, the absence of general systematic works, and the excessive confusion that pervaded the classification. Neither was it easy to decide on any satisfactory method of treating the subject. During the next two years, however, several important catalogues and systematic treatises appeared, which induced me to resume my work; and during the last three years it has occupied a large portion of my time. After much consideration, and some abortive trials, an outline plan of the book was matured; and as this is, so far as I am aware, quite novel, it will be well to give a few of the reasons for adopting it. Most of the previous writings on Geographical Distribution appeared to me to be unsatisfactory, because they drew their conclusions from a more or less extensive _selection_ of facts; and did not clearly separate groups of facts of unequal value, or those relating to groups of animals of unequal rank. As an example of what is meant, I may refer to Mr. Andrew Murray's large and valuable work on the Geographical Distribution of Mammalia, in which an immense number of coloured maps are used to illustrate the distribution of various groups of animals. These maps are not confined to groups of any fixed rank, but are devoted to a selection of groups of various grades. Some show the range of single species of a genus--as the lion, the tiger, the puma, and a species of fox; others are devoted to sections of genera,--as the true wolves; others to genera,--as the hyænas, and the bears; others to portions of families,--as the flying squirrels, and the oxen with the bisons; others to families,--as the Mustelidæ, and the Hystricidæ; and others to groups of families or to orders,--as the Insectivora, and the opossums with the kangaroos. But in no one grade are all the groups treated alike. Many genera are wholly unnoticed, while several families are only treated in combination with others, or are represented by some of the more important genera. In making these observations I by no means intend to criticise Mr. Murray's book, but merely to illustrate by an example, the method which has been hitherto employed, and which seems to me not well adapted to enable us to establish the foundations of the science of distribution on a secure basis. To do this, uniformity of treatment appeared to me essential, both as a matter of principle, and to avoid all imputation of a partial selection of facts, which may be made to prove anything. I determined, therefore, to take in succession every well-established family of terrestrial vertebrates, and to give an account of the distribution of all its component genera, as far as materials were available. Species, as such, are systematically disregarded,--firstly, because they are so numerous as to be unmanageable; and, secondly, because they represent the most recent modifications of form, due to a variety of often unknown causes, and are therefore not so clearly connected with geographical changes as are the natural groups of species termed genera; which may be considered to represent the average and more permanent distribution of an organic type, and to be more clearly influenced by the various known or inferred changes in the organic and physical environment. This systematic review of the distribution of families and genera, now forms the last part of my book--Geographical Zoology; but it was nearly the first written, and the copious materials collected for it enabled me to determine the zoo-geographical divisions of the earth (regions and sub-regions) to be adopted. I next drew up tables of the families and genera found in each region and sub-region; and this afforded a basis for the geographical treatment of the subject--Zoological Geography--the most novel, and perhaps the most useful and generally interesting part of my work. While this was in progress I found it necessary to make a careful summary of the distribution of extinct Mammalia. This was a difficult task, owing to the great uncertainty that prevails as to the affinities of many of the fossils, and my want of practical acquaintance with Palæontology; but having carefully examined and combined the works of the best authors, I have given what I believe is the first connected sketch of the relation of extinct Mammalia to the distribution of living groups, and have arrived at some very interesting and suggestive results. It will be observed that man is altogether omitted from the series of the animal kingdom as here given, and some explanation of this omission may perhaps be required. If the genus _Homo_ had been here treated like all other genera, nothing more than the bare statement--"universally distributed"--could have been given;--and this would inevitably have provoked the criticism that it conveyed no information. If, on the other hand, I had given an outline of the distribution of the _varieties_ or _races_ of man, I should have departed from the plan of my work for no sufficient reason. Anthropology is a science by itself; and it seems better to omit it altogether from a zoological work, than to treat it in a necessarily superficial manner. The best method of illustrating a work of this kind was a matter requiring much consideration. To have had a separate coloured or shaded map for each family would have made the work too costly, as the terrestrial vertebrates alone would have required more than three hundred maps. I had also doubts about the value of this mode of illustration, as it seemed rather to attract attention to details than to favour the development of general views. I determined therefore to adopt a plan, suggested in conversation by Professor Newton; and to have one general map, showing the regions and sub-regions, which could be referred to by means of a series of numbers. These references I give in the form of diagrammatic headings to each family; and, when the map has become familiar, these will, I believe, convey at a glance a body of important information. Taking advantage of the recent extension of our knowledge of the depths of the great oceans, I determined to give upon this map a summary of our knowledge of the contours of the ocean bed, by means of tints of colour increasing in intensity with the depth. Such a map, when it can be made generally accurate, will be of the greatest service in forming an estimate of the more probable changes of sea and land during the Tertiary period; and it is on the effects of such changes that any satisfactory explanation of the facts of distribution must to a great extent depend. Other important factors in determining the actual distribution of animals are, the zones of altitude above the sea level, and the strongly contrasted character of the surface as regards vegetation--a primary condition for the support of animal life. I therefore designed a series of six maps of the regions, drawn on a uniform scale, on which the belts of altitude are shown by contour-shading, while the forests, pastures, deserts, and perennial snows, are exhibited by means of appropriate tints of colour. These maps will, I trust, facilitate the study of geographical distribution as a science, by showing, in some cases, an adequate cause in the nature of the terrestrial surface for the actual distribution of certain groups of animals. As it is hoped they will be constantly referred to, double folding has been avoided, and they are consequently rather small; but Mr. Stanford, and his able assistant in the map department, Mr. Bolton, have taken great care in working out the details from the latest observations; and this, combined with the clearness and the beauty of their execution, will I trust render them both interesting and instructive. In order to make the book more intelligible to those readers who have no special knowledge of systematic zoology, and to whom most of the names with which its pages are often crowded must necessarily be unmeaning, I give a series of twenty plates, each one illustrating at once the physical aspect and the special zoological character of some well-marked division of a region. Great care has been taken to associate in the pictures, such species only as do actually occur together in nature; so that each plate represents a scene which is, at all events, not an impossible one. The species figured all belong to groups which are either peculiar to, or very characteristic of, the region whose zoology they illustrate; and it is hoped that these pictures will of themselves serve to convey a notion of the varied types of the higher animals in their true geographical relations. The artist, Mr. J. B. Zwecker, to whose talent as a zoological draughtsman and great knowledge both of animal and vegetable forms we are indebted for this set of drawings, died a few weeks after he had put the final touches to the proofs. He is known to many readers by his vigorous illustrations of the works of Sir Samuel Baker, Livingstone, and many other travellers,--but these, his last series of plates, were, at my special request, executed with a care, delicacy, and artistic finish, which his other designs seldom exhibit. It must, however, be remembered, that the figures of animals here given are not intended to show specific or generic characters for the information of the scientific zoologist, but merely to give as accurate an idea as possible, of some of the more remarkable and more restricted types of beast and bird, amid the characteristic scenery of their native country;--and in carrying out this object there are probably few artists who would have succeeded better than Mr. Zwecker has done. The general arrangement of the separate parts of which the work is composed, has been, to some extent, determined by the illustrations and maps, which all more immediately belong to Part III. It was at first intended to place this part last, but as this arrangement would have brought all the illustrations into the second volume, its place was changed,--perhaps in other respects for the better, as it naturally follows Part II. Yet for persons not well acquainted with zoology, it will perhaps be advisable to read the more important articles of Part IV. (and especially the observations at the end of each order) after Part II., thus making Part III. the conclusion of the work. Part IV. is, in fact, a book of reference, in which the distribution of all the families and most of the genera of the higher animals, is given in systematic order. Part III. is treated somewhat more popularly; and, although it is necessarily crowded with scientific names (without which the inferences and conclusions would have nothing solid to rest on), these may be omitted by the non-scientific reader, or merely noted as a certain number or proportion of peculiar generic types. Many English equivalents to family and generic names are, however, given; and, assisted by these, it is believed that any reader capable of understanding Lyell's "Principles," or Darwin's "Origin," will have no difficulty in following the main arguments and appreciating the chief conclusions arrived at in the present work. To those who are more interested in facts than in theories, the book will serve as a kind of dictionary of the geography and affinities of animals. By means of the copious Index, the native country, the systematic position, and the numerical extent of every important and well established genus of land-animal may be at once discovered;--information now scattered through hundreds of volumes. In the difficult matters of synonymy, and the orthography of generic names, I have been guided rather by general utility than by any fixed rules. When I have taken a whole family group from a modern author of repute, I have generally followed his nomenclature throughout. In other cases, I use the names which are to be found in a majority of modern authors, rather than follow the strict rule of priority in adopting some newly discovered appellation of early date. In orthography I have adopted all such modern emendations as seem coming into general use, and which do not lead to inconvenience; but where the alteration is such as to completely change the pronunciation and appearance of a well-known word, I have not adopted it. I have also thought it best to preserve the initial letter of well-known and old-established names, for convenience of reference to the Indices of established works. As an example I may refer to _Enicurus_,--a name which has been in use nearly half a century, and which is to be found under the letter _E_, in Jerdon's Birds of India, Blyth's Catalogue, Bonaparte's Conspectus, and the Proceedings of the Zoological Society of London down to 1865. Classicists now write _Henicurus_ as the correct form; but this seems to me one of those cases in which orthographical accuracy should give way to priority, and still more to convenience. In combining and arranging so much detail from such varied sources, many errors and omissions must doubtless have occurred. Owing to my residence at a distance from the scientific libraries of the metropolis, I was placed at a great disadvantage; and I could hardly have completed the work at all, had I not been permitted to have a large number of volumes at once, from the library of the Zoological Society of London, and to keep them for months together;--a privilege for which I return my best thanks to Mr. Sclater the Secretary, and to the Council. Should my book meet with the approval of working naturalists, I venture to appeal to them, to assist me in rendering any future editions more complete, by sending me (to the care of my publishers) notes of any important omissions, or corrections of any misstatements of fact; as well as copies of any of their papers or essays, and especially of any lists, catalogues, and monographs, containing information on the classification or distribution of living or extinct animals. To the many friends who have given me information or assistance I beg to tender my sincere thanks. Especially am I indebted to Professor Newton, who not only read through much of my rough MSS., but was so good as to make numerous corrections and critical notes. These were of great value to me, as they often contained or suggested important additional matter, or pointed out systematic and orthographical inaccuracies. Professor Flower was so good as to read over my chapters on extinct animals, and to point out several errors into which I had fallen. Dr. Günther gave me much valuable information on the classification of reptiles, marking on my lists the best established and most natural genera, and referring me to reliable sources of information. I am also greatly indebted to the following gentlemen for detailed information on special subjects:-- To Sir Victor Brooke, for a MS. arrangement of the genera of Bovidæ, with the details of their distribution: To Mr. Dresser, for lists of the characteristic birds of Northern and Arctic Europe: To Dr. Hooker, for information on the colours and odours of New Zealand plants: To Mr. Kirby, for a list of the butterflies of Chili: To Professor Mivart, for a classification of the Batrachia, and an early proof of his article on "Apes" in the Encyclopedia Britannica: To Mr. Salvin, for correcting my list of the birds of the Galapagos, and for other assistance: To Mr. Sharpe, for MS. lists of the birds of Madagascar and the Cape Verd Islands: To Canon Tristram, for a detailed arrangement of the difficult family of the warblers,--Sylviidæ: To Viscount Walden, for notes on the systematic arrangement of the Pycnonotidæ and Timaliidæ, and for an early proof of his list of the birds of the Philippine Islands. I also have to thank many naturalists, both in this country and abroad, who have sent me copies of their papers; and I trust they will continue to favour me in the same manner. An author may easily be mistaken in estimating his own work. I am well aware that this first outline of a great subject is, in parts, very meagre and sketchy; and, though perhaps overburthened with some kinds of detail, yet leaves many points most inadequately treated. It is therefore with some hesitation that I venture to express the hope that I have made some approach to the standard of excellence I have aimed at;--which was, that my book should bear a similar relation to the eleventh and twelfth chapters of the "Origin of Species," as Mr. Darwin's "Animals and Plants under Domestication" does to the first chapter of that work. Should it be judged worthy of such a rank, my long, and often wearisome labours, will be well repaid. MARCH, 1876. CONTENTS OF THE FIRST VOLUME. PART I. THE PRINCIPLES AND GENERAL PHENOMENA OF DISTRIBUTION. CHAPTER I. INTRODUCTORY. CHAPTER II. THE MEANS OF DISPERSAL AND THE MIGRATIONS OF ANIMALS. Means of Dispersal of Mammalia (p. 10)--Climate as a Limit to the Range of Mammals (p. 11)--Valleys and Rivers as Barriers to Mammals (p. 12)-- Arms of the Sea as Barriers to Mammals (p. 13)--Ice-floes and drift-wood as aiding the Dispersal of Mammals (p. 14)--Means of Dispersal of Birds (p. 15)--Dispersal of Birds by Winds (p. 16)--Barriers to the Dispersal of Birds (p. 17)--The Phenomena of Migration (p. 18)--Migrations of Birds (p. 19)--General remarks on Migration (p. 25)--Means of Dispersal of Reptiles and Amphibia (p. 28)--Means of Dispersal of Fishes (p. 29)-- Means of Dispersal of Mollusca (p. 30)--Means of Dispersal of Insects and the Barriers which limit their Range (p. 32) 10-34 CHAPTER III. DISTRIBUTION AS AFFECTED BY THE CONDITIONS AND CHANGES OF THE EARTH'S SURFACE. Land and Water (p. 35)--Continental Areas (p. 36)--Recent Changes in the Continental Areas (p. 38)--The Glacial Epoch as affecting the Distribution of Animals (p. 40)--Changes of Vegetation as affecting the Distribution of Animals (p. 43)--Organic Changes as affecting Distribution (p. 44) 35-49 CHAPTER IV. ON ZOOLOGICAL REGIONS. Principles upon which Zoological Regions should be formed (p. 53)--Which class of Animals is of most importance in determining Zoological Regions (p. 56)--Various Zoological Regions proposed since 1857 (p. 58)-- Discussion of proposed Regions (p. 61)--Reasons for adopting the Six Regions first proposed by Mr. Sclater (p. 63)--Objections to the system of Circumpolar Zones (p. 67)--Does the Arctic Fauna characterise an independent Region (p. 68)--Palæarctic Region (p. 71)--Ethiopian Region (p. 73)--Oriental Region (p. 75)--Australian Region (p. 77)--Neotropical Region (p. 78)--Nearctic Region (p. 79)--Observations on the series of Sub-regions (p. 80) 50-82 CHAPTER V. CLASSIFICATION AS AFFECTING THE STUDY OF GEOGRAPHICAL DISTRIBUTION. Classification of the Mammalia (p. 85)--Classification of Birds (p. 92)-- Classification of Reptiles (p. 98)--Classification of Amphibia (p. 100)-- Classification of Fishes (p. 101)--Classification of Insects (p. 102)-- Classification of Mollusca (p. 104) 83-104 PART II. ON THE DISTRIBUTION OF EXTINCT ANIMALS. CHAPTER VI. THE EXTINCT MAMMALIA OF THE OLD WORLD. Historic and Post-pliocene Period (p. 110)--Pliocene Period (p. 112)-- General Conclusions as to the Pliocene and Post-pliocene Faunas of Europe (p. 113)--Miocene Period (p. 114)--Extinct Animals of Greece (p. 115)-- Miocene Fauna of Central and Western Europe (p. 117)--Upper Miocene Deposits of India (p. 121)--General Observations on the Miocene Faunas of Europe and Asia (p. 123)--Eocene Period (p. 124)--General Considerations on the Extinct Mammalian Fauna of Europe (p. 126) 107-128 CHAPTER VII. EXTINCT MAMMALIA OF THE NEW WORLD. North America--Post-pliocene Period (p. 129)--Remarks on the Post- pliocene Fauna of North America (p. 130)--Tertiary Period (p. 132)-- Primates (p. 132)--Insectivora (p. 133)--Carnivora (p. 134)--Ungulata (p. 135)--Proboscidea (p. 138)--Tillodontia (p. 139)--Rodentia (p. 140)-- General Relations of the Extinct Tertiary Mammalia of North America and Europe (p. 140)--South America (p. 143)--Fauna of the Brazilian Caves (p. 143)--Pliocene Period of Temperate South America (p. 146)--Pliocene Mammalia of the Antilles (p. 148)--Eocene Fauna of South America (p. 148) --General Remarks on the Extinct Mammalian Fauna of the Old and New Worlds (p. 148)--The Birth-place and Migrations of some Mammalian Families and Genera (p. 153) 129-156 CHAPTER VIII. VARIOUS EXTINCT ANIMALS;--AND ON THE ANTIQUITY OF THE GENERA OF INSECTS AND LAND-MOLLUSCA. Extinct Mammalia of Australia (p. 157)--Mammalian Remains of the Secondary Formations (p. 159)--Extinct Birds (p. 160)--Palæarctic Region and North India (p. 161)--North America (p. 163)--South America, Madagascar, New Zealand (p. 164)--Extinct Tertiary Reptiles (p. 165)-- Antiquity of the Genera of Insects (p. 166)--Antiquity of the Genera of Land and Fresh-water Shells (p. 168) 157-170 PART III. ZOOLOGICAL GEOGRAPHY: A REVIEW OF THE CHIEF FORMS OF LIFE IN THE SEVERAL REGIONS AND SUB-REGIONS, WITH THE INDICATIONS THEY AFFORD OF GEOGRAPHICAL MUTATIONS. CHAPTER IX. THE ORDER OF SUCCESSION OF THE REGIONS.--COSMOPOLITAN GROUPS OF ANIMALS.--TABLES OF DISTRIBUTION. Order of succession of the Regions (p. 173)--Cosmopolitan Groups (p. 175) --Tables of Distributions of Families and Genera (p. 177) 173-179 CHAPTER X. THE PALÆARCTIC REGION. Zoological Characteristics of the Palæarctic Region (p. 181)--Summary of Palæarctic Vertebrata (p. 186)--Insects (p. 187)--Land-shells (p. 190)-- The Palæarctic Sub-regions (p. 190)--Central and Northern Europe (p. 191) --North European Islands (p. 197)--Mediterranean Sub-region (p. 199)-- The Mediterranean and Atlantic Islands (p. 206)--The Siberian Sub-region, or Northern Asia (p. 216)--Japan and North China, or the Manchurian Sub-region (p. 220)--Birds (p. 223)--Insects (p. 227)--Remarks on the General Character of the Fauna of Japan (p. 230)--General Conclusions as to the Fauna of the Palæarctic Region (p. 231)--Table I. Families of Animals inhabiting the Palæarctic Region (p. 234)--Table II. List of the Genera of Terrestrial Mammalia and Birds of the Palæarctic Region (p. 239) 181-250 CHAPTER XI. THE ETHIOPIAN REGION. Zoological Characteristics of the Ethiopian Region (p. 252)--Summary of Ethiopian Vertebrates (p. 255)--The Ethiopian Sub-regions (p. 258)--The East African Sub-region, or Central and East Africa (p. 258)--The West African Sub-region (p. 262)--Islands of the West African Sub-region (p. 265)--South African Sub-region (p. 266)--Atlantic Islands of the Ethiopian Region;--St. Helena (p. 269)--Tristan d'Acunha (p. 271)-- Madagascar and the Mascarene Islands, or the Malagasy Sub-region (p. 272) --The Mascarene Islands (p. 280)--Extinct Fauna of the Mascarene Islands and Madagascar (p. 282)--General Remarks on the Insect Fauna of Madagascar (p. 284)--On the probable Past History of the Ethiopian Region (p. 285)--Table I. Families of Animals inhabiting the Ethiopian Region (p. 294)--Table II. List of Genera of Terrestrial Mammalia and Birds of the Ethiopian Region (p. 300) 251-313 CHAPTER XII. THE ORIENTAL REGION. Zoological Characteristics of the Oriental Region (p. 315)--Summary of Oriental Vertebrata (p. 318)--The Oriental Sub-regions (p. 321)-- Hindostan, or Indian Sub-region (p. 321)--Range of the Genera of Mammalia which inhabit the Sub-region of Hindostan (p. 322)--Oriental, Palæarctic, and Ethiopian Genera of Birds in Central India (p. 224)--Sub-region of Ceylon and South India (p. 326)--The Past History of Ceylon and South India, as indicated by its Fauna (p. 328)--Himalayan or Indo-Chinese Sub-region (p. 329)--Islands of the Indo-Chinese Sub-region (p. 333)-- Indo-Malaya, or the Malayan Sub-region (p. 334)--Malayan Insects (p. 341) --The Zoological Relations of the several Islands of the Indo-Malay Sub-region (p. 345)--Philippine Islands (p. 345)--Java (p. 349)--Malacca, Sumatra, and Borneo (p. 353)--Probable recent Geographical Changes in the Indo-Malay Islands (p. 357)--Probable Origin of the Malayan Fauna (p. 359)--Concluding Remarks on the Oriental Region (p. 362)--Table I. Families of Animals inhabiting the Oriental Region (p. 365)--Table II. Genera of Terrestrial Mammalia and Birds in the Oriental Region (p. 371) 314-386 CHAPTER XIII. THE AUSTRALIAN REGION. General Zoological Characteristics of the Australian Region (p. 390)-- Summary of the Australian Vertebrata (p. 397)--Supposed Land-connection between Australia and South America (p. 398)--Insects (p. 403)-- Land-shells (p. 407)--Australian Sub-regions (p. 408)--Austro-Malayan Sub-region (p. 409)--Papua, or the New Guinea Group (p. 409)--The Moluccas (p. 417)--Insects--Peculiarities of the Moluccan Fauna (p. 420) --Timor Group (p. 422)--Celebes Group (p. 426)--Origin of the Fauna of Celebes (p. 436)--Australia and Tasmania, or the Australian Sub-region (p. 438)--The Pacific Islands, or Polynesian Sub-region (p. 442)--Fiji, Tonga, and Samoa Islands (p. 443)--Society and Marquesas Islands (p. 443) --Ladrone and Caroline Islands (p. 444)--New Caledonia and the New Hebrides (p. 444)--Sandwich Islands (p. 445)--Reptiles of the Polynesian Sub-region (p. 448)--New Zealand Sub-region (p. 449)--Islets of the New Zealand Sub-region (p. 453)--Reptiles, Amphibia, and Fresh-water Fishes (p. 456)--Insects (p. 457)--The Ancient Fauna of New Zealand (p. 459)-- The Origin of the New Zealand Fauna (p. 459)--Causes of the Poverty of Insect-life in New Zealand: its Influence on the Character of the Flora (p. 462)--Concluding Remarks on the Early History of the Australian Region (p. 464)--Table I. Families of Animals inhabiting the Australian Region (p. 468)--Table II. Genera of Terrestrial Mammalia and Birds of the Australian Region (p. 473) 387-485 Index to Vol. I 489-503 MAPS AND ILLUSTRATIONS IN VOL. I. 1. Map of the World, showing the Zoo-Geographical Regions and the contour of the Ocean-bed _Frontispiece_ _To face page_ 2. Map of the Palæarctic Region 181 3. Plate I. The Alps of Central Europe with Characteristic Animals 195 4. Plate II. Characteristic Mammalia of Western Tartary 218 5. Plate III. Characteristic Animals of North China 226 6. Map of the Ethiopian Region 251 7. Plate IV. Characteristic Animals of East Africa 261 8. Plate V. Scene in West Africa with Characteristic Animals 264 9. Plate VI. Scene in Madagascar with Characteristic Animals 278 10. Map of the Oriental Region 315 11. Plate VII. Scene in Nepaul with Characteristic Animals 331 12. Plate VIII. A Forest in Borneo with Characteristic Mammalia 337 13. Plate IX. A Malacca Forest with some of its Peculiar Birds 340 14. Map of the Australian Region 387 15. Plate X. Scene in New Guinea with Characteristic Animals 415 16. Plate XI. The Characteristic Mammalia of Tasmania 439 17. Plate XII. The Plains of New South Wales with Characteristic Animals 442 18. Plate XIII. Scene in New Zealand with some of its Remarkable Birds 455 ERRATA IN VOL. I. I have detected several misprints and small errors in the final impression, and Dr. Meyer, who has translated the work into German, has kindly communicated all that he has noticed. It is not thought necessary to give here all the smaller orthographical errors, most of which will be corrected in the Index. The following seem, however, to be of sufficient importance to justify me in asking my readers to correct them in their copies. Page 93, 12 lines from foot, _for_ Hocco _read_ Hoazin. " 97, line 2, _for_ Hocco _read_ Hoazin. " 147, 13 lines from foot, _for_ three-handed _read_ three-banded. " 177, line 6, _for_ Lycænidæ _read_ Zygænidæ. " 183, line 20, _for_ third _read_ fourth. " 238, line 18, _for_ Spirigidea _read_ Sphingidea. " 242, _insert_ | 92a | Tamias | 1 | All Northern Asia | N. America. " 245, last line, _insert in 2nd column_ (6). " 309, line 20, _for_ Motacilla _read_ Budytes. " 327, 12 lines from foot, _after_ Hindostan _read_ and. " 331, last line, for _Icthyopsis_ read _Icthyophis_. " 340, line 15, for _Edolius_ read _Bhringa_. " 348, line 17, _for_ Flores _read_ New Guinea. " 371, 11 lines from foot, _for_ and Borneo _read_ Borneo and Philippines. " 391, 10 lines from foot, _after_ Celebes _add_ and the Papuan Islands. " 391, 9 lines from foot, _omit_ New Guinea or. " 414, 6 lines from foot, for _Epimachus_ read _Seleucides_. " 415, line 10 _for_ ditto _read_ ditto. " 427, line 20, _after_ Celebes _add_ and on some of the Philippine Islands. " 427, 5 lines from foot, _for_ tusks _read_ jaw. " 462, 15 lines from foot, _for_ p. 156 _read_ p. 166. " 474, 9 lines from foot, _after_ Celebes _add_ Papua. THE GEOGRAPHICAL DISTRIBUTION OF ANIMALS. PART I. _THE PRINCIPLES AND GENERAL PHENOMENA OF DISTRIBUTION._ {3}CHAPTER I. INTRODUCTORY. It is a fact within the experience of most persons, that the various species of animals are not uniformly dispersed over the surface of the country. If we have a tolerable acquaintance with any district, be it a parish, a county, or a larger extent of territory, we soon become aware that each well-marked portion of it has some peculiarities in its animal productions. If we want to find certain birds or certain insects, we have not only to choose the right season but to go to the right place. If we travel beyond our district in various directions we shall almost certainly meet with something new to us; some species which we were accustomed to see almost daily will disappear, others which we have never seen before will make their appearance. If we go very far, so as to be able to measure our journey by degrees of latitude and longitude and to perceive important changes of climate and vegetation, the differences in the forms of animal life will become greater; till at length we shall come to a country where almost everything will be new, all the familiar creatures of our own district being replaced by others more or less differing from them. If we have been observant during our several journeys, and have combined and compared the facts we have collected, it will become apparent that the change we have witnessed has been of two distinct kinds. In our own and immediately surrounding districts, particular species appeared and disappeared because {4}the soil, the aspect, or the vegetation, was adapted to them or the reverse. The marshes, the heaths, the woods and forests, the chalky downs, the rocky mountains, had each their peculiar inhabitants, which reappeared again and again as we came to tracts of country suitable for them. But as we got further away we began to find that localities very similar to those we had left behind were inhabited by a somewhat different set of species; and this difference increased with distance, notwithstanding that almost identical external conditions might be often met with. The first class of changes is that of _stations_; the second that of _habitats_. The one is a _local_, the other a _geographical_ phenomenon. The whole area over which a particular animal is found may consist of any number of _stations_, but rarely of more than one _habitat_. Stations, however, are often so extensive as to include the entire range of many species. Such are the great seas and oceans, the Siberian or the Amazonian forests, the North African deserts, the Andean or the Himalayan highlands. There is yet another difference in the nature of the change we have been considering. The new animals which we meet with as we travel in any direction from our starting point, are some of them very much like those we have left behind us, and can be at once referred to familiar types; while others are altogether unlike anything we have seen at home. When we reach the Alps we find another kind of squirrel, in Southern Italy a distinct mole, in Southern Europe fresh warblers and unfamiliar buntings. We meet also with totally new forms; as the glutton and the snowy owl in Northern, the genet and the hoopoe in Southern, and the saiga antelope and collared pratincole in Eastern Europe. The first series are examples of what are termed _representative species_, the second of distinct groups or _types_ of animals. The one represents a comparatively recent modification, and an origin in or near the locality where it occurs; the other is a result of very ancient changes both organic and inorganic, and is connected with some of the most curious and difficult of the problems we shall have to discuss. {5}Having thus defined our subject, let us glance at the opinions that have generally prevailed as to the nature and causes of the phenomena presented by the geographical distribution of animals. It was long thought, and is still a popular notion, that the manner in which the various kinds of animals are dispersed over the globe is almost wholly due to diversities of climate and of vegetation. There is indeed much to favour this belief. The arctic regions are strongly characterised by their white bears and foxes, their reindeer, ermine, and walruses, their white ptarmigan, owls, and falcons; the temperate zone has its foxes and wolves, its rabbits, sheep, beavers, and marmots, its sparrows and its song birds; while tropical regions alone produce apes and elephants, parrots and peacocks, and a thousand strange quadrupeds and brilliant birds which are found nowhere in the cooler regions. So the camel, the gazelle and the ostrich live in the desert; the bison on the prairie; the tapir, the deer, and the jaguar in forests. Mountains and marshes, plains and rocky precipices, have each their animal inhabitants; and it might well be thought, in the absence of accurate inquiry, that these and other differences would sufficiently explain why most of the regions and countries into which the earth is popularly divided should have certain animals peculiar to them and should want others which are elsewhere abundant. A more detailed and accurate knowledge of the productions of different portions of the earth soon showed that this explanation was quite insufficient; for it was found that countries exceedingly similar in climate and all physical features may yet have very distinct animal populations. The equatorial parts of Africa and South America, for example, are very similar in climate and are both covered with luxuriant forests, yet their animal life is widely different; elephants, apes, leopards, guinea-fowls and touracos in the one, are replaced by tapirs, prehensile-tailed monkeys, jaguars, curassows and toucans in the other. Again, parts of South Africa and Australia are wonderfully similar in their soil and climate; yet one has lions, antelopes, zebras and giraffes; the other only kangaroos, wombats, {6}phalangers and mice. In like manner parts of North America and Europe are very similar in all essentials of soil climate and vegetation, yet the former has racoons, opossums, and humming-birds; while the latter possesses moles, hedgehogs and true flycatchers. Equally striking are the facts presented by the distribution of many large and important groups of animals. Marsupials (opossums, phalangers &c.) are found from temperate Van Diemen's land to the tropical islands of New Guinea and Celebes, and in America from Chili to Virginia. No crows exist in South America, while they inhabit every other part of the world, not excepting Australia. Antelopes are found only in Africa and Asia; the sloths only in South America; the true lemurs are confined to Madagascar, and the birds-of-paradise to New Guinea. If we examine more closely the distribution of animals in any extensive region, we find that different, though closely allied species, are often found on the opposite sides of any considerable barrier to their migration. Thus, on the two sides of the Andes and Rocky Mountains in America, almost all the mammalia, birds, and insects are of distinct species. To a less extent, the Alps and Pyrenees form a similar barrier, and even great rivers and river plains, as those of the Amazon and Ganges, separate more or less distinct groups of animals. Arms of the sea are still more effective, if they are permanent; a circumstance in some measure indicated by their depth. Thus islands far away from land almost always have very peculiar animals found nowhere else; as is strikingly the case in Madagascar and New Zealand, and to a less degree in the West India islands. But shallow straits, like the English Channel or the Straits of Malacca, are not found to have the same effect, the animals being nearly or quite identical on their opposite shores. A change of climate or a change of vegetation may form an equally effective barrier to migration. Many tropical and polar animals are pretty accurately limited by certain isothermal lines; and the limits of the great forests in most parts of the world strictly determine the ranges of many species. Naturalists have now arrived at the conclusion, that by some {7}slow process of development or transmutation, all animals have been produced from those which preceded them; and the old notion that every species was specially created as they now exist, at a particular time and in a particular spot, is abandoned as opposed to many striking facts, and unsupported by any evidence. This modification of animal forms took place very slowly, so that the historical period of three or four thousand years has hardly produced any perceptible change in a single species. Even the time since the last glacial epoch, which on the very lowest estimate must be from 50,000 to 100,000 years, has only served to modify a few of the higher animals into very slightly different species. The changes of the forms of animals appear to have accompanied, and perhaps to have depended on, changes of physical geography, of climate, or of vegetation; since it is evident that an animal which is well adapted to one condition of things will require to be slightly changed in constitution or habits, and therefore generally in form, structure, or colour, in order to be equally well adapted to a changed condition of surrounding circumstances. Animals multiply so rapidly, that we may consider them as continually trying to extend their range; and thus any new land raised above the sea by geological causes becomes immediately peopled by a crowd of competing inhabitants, the strongest and best adapted of which alone succeed in maintaining their position. If we keep in view these facts--that the minor features of the earth's surface are everywhere slowly changing; that the forms, and structure, and habits of all living things are also slowly changing; while the great features of the earth, the continents, and oceans, and loftiest mountain ranges, only change after very long intervals and with extreme slowness; we must see that the present distribution of animals upon the several parts of the earth's surface is the final product of all these wonderful revolutions in organic and inorganic nature. The greatest and most radical differences in the productions of any part of the globe must be dependent on isolation by the most effectual and most permanent barriers. That ocean which has remained broadest and deepest from the most remote geological epoch {8}will separate countries the productions of which most widely and radically differ; while the most recently-depressed seas, or the last-formed mountain ranges, will separate countries the productions of which are almost or quite identical. It will be evident, therefore, that the study of the distribution of animals and plants may add greatly to our knowledge of the past history of our globe. It may reveal to us, in a manner which no other evidence can, which are the oldest and most permanent features of the earth's surface, and which the newest. It may indicate the existence of islands or continents now sunk beneath the ocean, and which have left no record of their existence save the animal and vegetable productions which have migrated to adjacent lands. It thus becomes an important adjunct to geology, which can rarely do more than determine what lands have been raised above the waters, under what conditions and at what period; but can seldom ascertain anything of the position or extent of those which have sunk beneath it. Our present study may often enable us, not only to say where lands must have recently disappeared, but also to form some judgment as to their extent, and the time that has elapsed since their submersion. Having thus briefly sketched the nature and objects of the subject we have to study, it will be necessary--before entering on a detailed examination of the zoological features of the different parts of the earth, and of the distribution of the orders, families, and genera of animals--to examine certain preliminary facts and principles essential for our guidance. We must first inquire what are the powers of multiplication and dispersal of the various groups of animals, and the nature of the barriers that most effectually limit their range. We have then to consider the effects of changes in physical geography and in climate; to examine the nature and extent of such changes as have been known to occur; to determine what others are possible or probable; and to ascertain the various modes in which such changes affect the structure, the distribution, or the very existence of animals. {9}Two subjects of a different nature must next engage our attention. We have to deal with two vast masses of facts, each involving countless details, and requiring subdivision and grouping to be capable of intelligible treatment. All the continents and their chief subdivisions, and all the more important islands of the globe, have to be compared as regards their various animal forms. To do this effectively we require a natural division of the earth especially adapted to our purpose; and we shall have to discuss at some length the reasons for the particular system adopted,--a discussion which must to some extent anticipate and summarize the conclusions of the whole work. We have also to deal with many hundreds of families and many thousands of genera of animals, and here too a true and natural classification is of great importance. We must therefore give a connected view of the classification adopted in the various classes of animals dealt with. And lastly, as the existing distribution of animals is the result and outcome of all preceding changes of the earth and of its inhabitants, we require as much knowledge as we can get of the animals of each country during past geological epochs, in order to interpret the facts we shall accumulate. We shall, therefore, enter upon a somewhat detailed sketch of the various forms of extinct animals that have lived upon the earth during the Tertiary period; discuss their migrations at various epochs, the changes of physical geography that they imply, and the extent to which they enable us to determine the birthplace of certain families and genera. The preliminary studies above enumerated will, it is believed, enable us to see the bearing of many facts in the distribution of animals that would otherwise be insoluble problems; and, what is hardly less valuable, will teach us to estimate the comparative importance of the various groups of animals, and to avoid the common error of cutting the gordian knot of each difficulty by vast hypothetical changes in existing continents and oceans--probably the most permanent features of our globe. {10}CHAPTER II. THE MEANS OF DISPERSAL AND THE MIGRATIONS OF ANIMALS. All animals are capable of multiplying so rapidly, that if a single pair were placed in a continent with abundance of food and no enemies, they might fully stock it in a very short time. Thus, a bird which produces ten pairs of young during its lifetime (and this is far below the fertility of many birds) will, if we take its life at five years, increase to a hundred millions in about forty years, a number sufficient to stock a large country. Many fishes and insects are capable of multiplying several thousandfold each year, so that in a few years they would reach billions and trillions. Even large and slow breeding mammals, which have only one at a birth but continue to breed from eight to ten successive years, may increase from a single pair to ten millions in less than forty years. But as animals rarely have an unoccupied country to breed in, and as the food in any one district is strictly limited, their natural tendency is to roam in every direction in search of fresh pastures, or new hunting grounds. In doing so, however, they meet with many obstacles. Rocks and mountains have to be climbed, rivers or marshes to be crossed, deserts or forests to be traversed; while narrow straits or wider arms of the sea separate islands from the main land or continents from each other. We have now to inquire what facilities the different classes of animals have for overcoming these obstacles, and what kind of barriers are most effectual in checking their progress. _Means of Dispersal of Mammalia._--Many of the largest mammalia are able to roam over whole continents and are hardly {11}stopped by any physical obstacles. The elephant is almost equally at home on plains and mountains, and it even climbs to the highest summit of Adam's Peak in Ceylon, which is so steep and rocky as to be very difficult of ascent for man. It traverses rivers with great ease and forces its way through the densest jungle. There seems therefore to be no limit to its powers of wandering, but the necessity of procuring food and its capacity of enduring changes of climate. The tiger is another animal with great powers of dispersal. It crosses rivers and sometimes even swims over narrow straits of the sea, and it can endure the severe cold of North China and Tartary as well as the heats of the plains of Bengal. The rhinoceros, the lion, and many of the ruminants have equal powers of dispersal; so that wherever there is land and sufficient food, there are no limits to their possible range. Other groups of animals are more limited in their migrations. The apes, lemurs, and many monkeys are so strictly adapted to an arboreal life that they can never roam far beyond the limits of the forest vegetation. The same may be said of the squirrels, the opossums, the arboreal cats, and the sloths, with many other groups of less importance. Deserts or open country are equally essential to the existence of others. The camel, the hare, the zebra, the giraffe and many of the antelopes could not exist in a forest country any more than could the jerboas or the prairie marmots. There are other animals which are confined to mountains, and could not extend their range into lowlands or forests. The goats and the sheep are the most striking group of this kind, inhabiting many of the highest mountains of the globe; of which the European ibex and mouflon are striking examples. Rivers are equally necessary to the existence of others, as the beaver, otter, water-vole and capybara; and to such animals high mountain-ranges or deserts must form an absolutely impassable barrier. _Climate as a Limit to the Range of Mammals._--Climate appears to limit the range of many animals, though there is some reason to believe that in many cases it is not the climate itself so much as the change of vegetation consequent on climate which produces the effect. The quadrumana appear to be limited by climate, {12}since they inhabit almost all the tropical regions but do not range more than about 10° beyond the southern and 12° beyond the northern tropic, while the great bulk of the species are found only within an equatorial belt about 30° wide. But as these animals are almost exclusively fruit-eaters, their distribution depends as much on vegetation as on temperature; and this is strikingly shown by the fact that the _Semnopithecus schistaceus_ inhabits the Himalayan mountains to a height of 11,000 feet, where it has been seen leaping among fir-trees loaded with snow-wreaths! Some northern animals are bounded by the isothermal of 32°. Such are the polar bear and the walrus, which cannot live in a state of nature far beyond the limits of the frozen ocean; but as they live in confinement in temperate countries, their range is probably limited by other conditions than temperature. We must not therefore be too hasty in concluding, that animals which we now see confined to a very hot or a very cold climate are incapable of living in any other. The tiger was once considered a purely tropical animal, but it inhabits permanently the cold plains of Manchuria and the Amoor, a country of an almost arctic winter climate. Few animals seem to us more truly inhabitants of hot countries than the elephants and rhinoceroses; yet in Post-tertiary times they roamed over the whole of the northern continents to within the arctic circle; and we know that the climate was then as cold as it is now, from their entire bodies being preserved in ice. Some change must recently have occurred either in the climate, soil, or vegetation of Northern Asia which led to the extinction of these forerunners of existing tropical species; and we must always bear in mind that similar changes may have acted upon other species which we now find restricted within narrow limits, but which may once have roamed over a wide and varied territory. _Valleys and Rivers as Barriers to Mammals._--To animals which thrive best in dry and hilly regions, a broad level and marshy valley must often prove an effectual barrier. The difference of vegetation and of insect life, together with an unhealthy atmosphere, no doubt often checks migration if it is attempted. Thus {13}many animals are restricted to the slopes of the Himalayas or to the mountains of Central India, the flat valley of the Ganges forming a limit to their range. In other cases, however, it is the river rather than the valley which is the barrier. In the great Amazonian plains many species of monkeys, birds, and even insects are found up to the river banks on one side but do not cross to the other. Thus in the lower part of the Rio Negro two monkeys, the _Jacchus bicolor_ and the _Brachiurus couxiou_, are found on the north bank of the river but never on the south, where a red-whiskered _Pithecia_ is alone found. Higher up _Ateles paniscus_ extends to the north bank of the river while _Lagothrix humboldtii_ comes down to the south bank; the former being a native of Guiana, the latter of Ecuador. The range of the birds of the genus _Psophia_ or trumpeters, is also limited by the rivers Amazon, Madeira, Rio Negro and some others; so that in these cases we are able to define the limits of distribution with an unusual degree of accuracy, and there is little doubt the same barriers also limit a large number of other species. _Arms of the Sea as Barriers to Mammals._--Very few mammals can swim over any considerable extent of sea, although many can swim well for short distances. The jaguar traverses the widest streams in South America, and the bear and bison cross the Mississippi; and there can be no doubt that they could swim over equal widths of salt water, and if accidentally carried out to sea might sometimes succeed in reaching islands many miles distant. Contrary to the common notion pigs can swim remarkably well. Sir Charles Lyell tells us in his "Principles of Geology" that during the floods in Scotland in 1829, some pigs only six months old that were carried out to sea, swam five miles and got on shore again. He also states, on the authority of the late Edward Forbes, that a pig jumped overboard to escape from a terrier in the Grecian Archipelago, and swam safely to shore many miles distant. These facts render it probable that wild pigs, from their greater strength and activity, might under favourable circumstances cross arms of the sea twenty or thirty miles wide; and there are facts in the distribution of this tribe of animals which seem to indicate that they have sometimes done so. Deer {14}take boldly to the water and can swim considerable distances, but we have no evidence to show how long they could live at sea or how many miles they could traverse. Squirrels, rats, and lemmings often migrate from northern countries in bands of thousands and hundreds of thousands, and pass over rivers, lakes and even arms of the sea, but they generally perish in the saltwater. Admitting, however, the powers of most mammals to swim considerable distances, we have no reason to believe that any of them could traverse without help straits of upwards of twenty miles in width, while in most cases a channel of half that distance would prove an effectual barrier. _Ice-floes and Driftwood as Aiding the Dispersal of Mammals._--In the arctic regions icebergs originate in glaciers which descend into the sea, and often bear masses of gravel, earth, and even some vegetation on their surfaces; and extensive level ice-fields break away and float southwards. These might often carry with them such arctic quadrupeds as frequent the ice, or even on rare occasions true land-animals, which might sometimes be stranded on distant continents or islands. But a more effectual because a more wide-spread agent, is to be found in the uprooted trees and rafts of driftwood often floated down great rivers and carried out to sea. Such rafts or islands are sometimes seen drifting a hundred miles from the mouth of the Ganges with living trees erect upon them; and the Amazon, the Orinoco, Mississippi, Congo, and most great rivers produce similar rafts. Spix and Martius declare that they saw at different times on the Amazon, monkeys, tiger-cats, and squirrels, being thus carried down the stream. On the Parana, pumas, squirrels, and many other quadrupeds have been seen on these rafts; and Admiral W. H. Smyth informed Sir C. Lyell that among the Philippine islands after a hurricane, he met with floating masses of wood with trees growing upon them, so that they were at first mistaken for islands till it was found that they were rapidly drifting along. Here therefore, we have ample means for carrying all the smaller and especially the arboreal mammals out to sea; and although in most cases they would perish there, yet in some favourable instances strong winds or {15}unusual tidal currents might carry them safely to shores perhaps several hundred miles from their native country. The fact of green trees so often having been seen erect on these rafts is most important; for they would act as a sail by which the raft might he propelled in one direction for several days in succession, and thus at last reach a shore to which a current alone would never have carried it. There are two groups of mammals which have quite exceptional means of dispersal--the bats which fly, and the cetacea, seals, &c., which swim. The former are capable of traversing considerable spaces of sea, since two North American species either regularly or occasionally visit the Bermudas, a distance of 600 miles from the mainland. The oceanic mammals (whales and porpoises) seem to have no barrier but temperature; the polar species being unable to cross the equator, while the tropical forms are equally unfitted for the cold polar waters. The shore-feeding manatees, however, can only live where they find food; and a long expanse of rocky coast would probably be as complete a barrier to them as a few hundred miles of open ocean. The amphibious seals and walruses seem many of them to be capable of making long sea journeys, some of the species being found on islands a thousand miles apart, but none of the arctic are identical with the antartic species. The otters with one exception are freshwater animals, and we have no reason to believe they could or would traverse any great distances of salt water. In fact, they would be less liable to dispersal across arms of the sea than purely terrestrial species, since their powers of swimming would enable them to regain the shore if accidentally carried out to sea by a sudden flood. _Means of Dispersal of Birds._--It would seem at first sight that no barriers could limit the range of birds, and that they ought to be the most ubiquitous of living things, and little fitted therefore to throw any light on the laws or causes of the geographical distribution of animals. This, however, is far from being the case; many groups of birds are almost as strictly limited by barriers as the mammalia; and from their larger numbers and the avidity with which they have been collected, they furnish {16}materials of the greatest value for our present study. The different groups of birds offer remarkable contrasts in the extent of their range, some being the most cosmopolite of the higher animals, while others are absolutely confined to single spots on the earth's surface. The petrels (_Procellariidæ_) and the gulls (_Laridæ_) are among the greatest wanderers; but most of the species are confined to one or other of the great oceans, or to the arctic or antarctic seas, a few only being found with scarcely any variation over almost the whole globe. The sandpipers and plovers wander along the shores as far as do the petrels over the ocean. Great numbers of them breed in the arctic regions and migrate as far as India and Australia, or down to Chili and Brazil; the species of the old and new worlds, however, being generally distinct. In striking contrast to these wide ranges we find many of the smaller perching birds, with some of the parrots and pigeons, confined to small islands of a few square miles in extent, or to single valleys or mountains on the mainland. _Dispersal of Birds by Winds._--Those groups of birds which possess no powers of flight, such as the ostrich, cassowary, and apteryx, are in exactly the same position as mammalia as regards their means of dispersal, or are perhaps even inferior to them; since, although they are able to cross rivers by swimming, it is doubtful if they could remain so long in the water as most land quadrupeds. A very large number of short-winged birds, such as toucans, pittas, and wrens, are perhaps worse off; for they can fly very few miles at a time, and on falling into the water would soon be drowned. It is only the strong-flying species that can venture to cross any great width of sea; and even these rarely do so unless compelled by necessity to migrate in search of food, or to a more genial climate. Small and weak birds are, however, often carried accidentally across great widths of ocean by violent gales. This is well exemplified by the large numbers of stragglers from North America, which annually reach the Bermudas. No less than sixty-nine species of American birds have occurred in Europe, most of them in Britain and Heligoland. They consist chiefly of migratory birds which in autumn {17}return along the eastern coasts of the United States, and often fly from point to point across bays and inlets. They are then liable to be blown out to sea by storms, which are prevalent at this season; and it is almost always at this time of year that their occurrence has been noted on the shores of Europe. It may, however, be doubted whether this is not an altogether modern phenomenon, dependent on the number of vessels constantly on the Atlantic which afford resting-places to the wanderers; as it is hardly conceivable that such birds as titlarks, cuckoos, wrens, warblers, and rails, could remain on the wing without food or rest, the time requisite to pass over 2,000 miles of ocean. It is somewhat remarkable that no European birds reach the American coast but a few which pass by way of Iceland and Greenland; whereas a considerable number do reach the Azores, fully half way across; so that their absence can hardly be due to the prevailing winds being westerly. The case of the Azores is, however, an argument for the unassisted passage of birds for that distance; since two of the finches are peculiar 'species,' but closely allied to European forms, so that their progenitors must, probably, have reached the islands before the Atlantic was a commercial highway. _Barriers to the Dispersal of Birds._--We have seen that, as a rule, wide oceans are an almost absolute barrier to the passage of most birds from one continent to another; but much narrower seas and straits are also very effectual barriers where the habits of the birds are such as to preserve them from being carried away by storms. All birds which frequent thickets and forests, and which feed near or on the ground, are secure from such accidents; and they are also restricted in their range by the extent of the forests they inhabit. In South America a large number of the birds have their ranges determined by the extent of the forest country, while others are equally limited to the open plains. Such species are also bounded by mountain ranges whenever these rise above the woody region. Great rivers, such as the Amazon, also limit the range of many birds, even when there would seem to be no difficulty in their crossing them. The supply of food, and the kind of vegetation, soil, and climate {18}best suited to a bird's habits, are probably the causes which mark out the exact limits of the range of each species; to which must be added the prevalence of enemies of either the parent birds, the eggs, or the young. In the Malay Archipelago pigeons abound most where monkeys do not occur; and in South America the same birds are comparatively scarce in the forest plains where monkeys are very abundant, while they are plentiful on the open plains and campos, and on the mountain plateaux, where these nest-hunting quadrupeds are rarely found. Some birds are confined to swamps, others to mountains; some can only live on rocky streams, others on deserts or grassy plains. _The Phenomena of Migration._--The term "migration" is often applied to the periodical or irregular movements of all animals; but it may be questioned whether there are any regular migrants but birds and fishes. The annual or periodical movements of mammalia are of a different class. Monkeys ascend the Himalayas in summer to a height of 10,000 to 12,000 feet, and descend again in winter. Wolves everywhere descend from the mountains to the lowlands in severe weather. In dry seasons great herds of antelopes move southwards towards the Cape of Good Hope. The well-known lemmings, in severe winters, at long intervals, move down from the mountains of Scandinavia in immense numbers, crossing lakes and rivers, eating their way through haystacks, and surmounting every obstacle till they reach the sea, whence very few return. The alpine hare, the arctic fox, and many other animals, exhibit similar phenomena on a smaller scale; and generally it may be said, that whenever a favourable succession of seasons has led to a great multiplication of any species, it must on the pressure of hunger seek food in fresh localities. For such movements as these we have no special term. The summer and winter movements best correspond to true migration, but they are always on a small scale, and of limited extent; the other movements are rather temporary incursions than true migrations. The annual movements of many fishes are more strictly analogous to the migration of birds, since they take place in large bodies and often to considerable distances, and are {19}immediately connected with the process of reproduction. Some, as the salmon, enter rivers; others, as the herring and mackerel, approach the coast in the breeding season; but the exact course of their migrations is unknown, and owing to our complete ignorance of the area each species occupies in the ocean, and the absence of such barriers and of such physical diversities as occur on the land, they are of far less interest and less connected with our present study than the movements of birds, to which we shall now confine ourselves. _Migrations of Birds._--In all the temperate parts of the globe there are a considerable number of birds which reside only a part of the year, regularly arriving and leaving at tolerably fixed epochs. In our own country many northern birds visit us in winter, such as the fieldfare, redwing, snow-bunting, turnstone, and numerous ducks and waders; with a few, like the black redstart, and (according to Rev. C. A. Johns) some of the woodcocks from the south. In the summer a host of birds appear--the cuckoo, the swifts and swallows, and numerous warblers, being the most familiar,--which stay to build their nests and rear their young, and then leave us again. These are true migrants; but a number of other birds visit us occasionally, like the waxwing, the oriole, and the beefeater, and can only be classed as stragglers, which, perhaps from too rapid multiplication one year and want of food the next, are driven to extend their ordinary range of migration to an unusual degree. We will now endeavour to sketch the chief phenomena of migration in different countries. _Europe._--It is well ascertained that most of the birds that spend their spring and summer in the temperate parts of Europe pass the winter in North Africa and Western Asia. The winter visitants, on the other hand, pass the summer in the extreme north of Europe and Asia, many of them having been found to breed in Lapland. The arrival of migratory birds from the south is very constant as to date, seldom varying more than a week or two, without any regard to the weather at the time; but the departure is less constant, and more dependent on the weather. Thus the swallow always comes to us about the middle {20}of April, however cold it may be, while its departure may take place from the end of September to late in October, and is said by Forster to occur on the first N. or N.E. wind after the 20th of September. Almost all the migratory birds of Europe go southward to the Mediterranean, move along its coasts east or west, and cross over in three places only; either from the south of Spain, in the neighbourhood of Gibraltar, from Sicily over Malta, or to the east by Greece and Cyprus. They are thus always in sight of land. The passage of most small birds (and many of the larger ones too) takes place at night; and they only cross the Mediterranean when the wind is steady from near the east or west, and when there is moonlight. It is a curious fact, but one that seems to be well authenticated, that the males often leave before the females, and both before the young birds, which in considerable numbers migrate later and alone. These latter, however, seldom go so far as the old ones; and numbers of young birds do not cross the Mediterranean, but stay in the south of Europe. The same rule applies to the northward migration; the young birds stopping short of the extreme arctic regions, to which the old birds migrate.[1] When old and young go together, however, the old birds take the lead. In the south of Europe few of the migratory birds stay to breed, but pass on to more temperate zones; thus, in the south of France, out of 350 species only 60 breed there. The same species is often sedentary in one part of Europe and migratory in another; thus, the chaffinch is a constant resident in England, Germany, and the middle of France; but a migrant in the south of France and in Holland: the rook visits the south of France in winter only: the _Falco tinnunculus_ is both a resident and a migrant in the south of France, according to M. Marcel de Serres, there being two regular passages every year, while a certain number always remain. {21}We see, then, that migration is governed by certain intelligible laws; and that it varies in many of its details, even in the same species, according to changed conditions. It may be looked upon as an exaggeration of a habit common to all locomotive animals, of moving about in search of food. This habit is greatly restricted in quadrupeds by their inability to cross the sea or even to pass through the highly-cultivated valleys of such countries as Europe; but the power of flight in birds enables them to cross every kind of country, and even moderate widths of sea; and as they mostly travel at night and high in the air, their movements are difficult to observe, and are supposed to be more mysterious than they perhaps are. In the tropics birds move about to different districts according as certain fruits become ripe, certain insects abundant, or as flooded tracts dry up. On the borders of the tropics and the temperate zone extends a belt of country of a more or less arid character, and liable to be parched at the summer solstice. In winter and early spring its northern margin is verdant, but it soon becomes burnt up, and most of its birds necessarily migrate to the more fertile regions to the north of them. They thus follow the spring or summer as it advances from the south towards the pole, feeding on the young flower buds, the abundance of juicy larvæ, and on the ripening fruits; and as soon as these become scarce they retrace their steps homewards to pass the winter. Others whose home is nearer the pole are driven south by cold, hunger, and darkness, to more hospitable climes, returning northward in the early summer. As a typical example of a migratory bird, let us take the nightingale. During the winter this bird inhabits almost all North Africa, Asia Minor, and the Jordan Valley. Early in April it passes into Europe by the three routes already mentioned, and spreads over France, Britain, Denmark, and the south of Sweden, which it reaches by the beginning of May. It does not enter Brittany, the Channel Islands, or the western part of England, never visiting Wales, except the extreme south of Glamorganshire, and rarely extending farther north than Yorkshire. It spreads over Central Europe, through Austria and Hungary to Southern Russia and the warmer parts of Siberia, {22}but it nevertheless breeds in the Jordan Valley, so that in some places it is only the surplus population that migrates. In August and September, all who can return to their winter quarters. Migrations of this type probably date back from at least the period when there was continuous land along the route passed over; and it is a suggestive fact that this land connection is known to have existed in recent geological times. Britain was connected with the Continent during, and probably before, the glacial epoch; and Gibraltar, as well as Sicily and Malta, were also recently united with Africa, as is proved by the fossil elephants and other large mammalia found in their caverns, by the comparatively shallow water still existing in this part of the Mediterranean while the remainder is of oceanic profundity, and by the large amount of identity in the species of land animals still inhabiting the opposite shores of the Mediterranean. The submersion of these two tracts of land (which were perhaps of considerable extent) would be a slow process, and from year to year the change might be hardly perceptible. It is easy to see how the migration that had once taken place over continuous land would be kept up, first over lagoons and marshes, then over a narrow channel, and subsequently over a considerable sea, no one generation of birds ever perceiving any difference in the route. There is, however, no doubt that the sea-passage is now very dangerous to many birds. Quails cross in immense flocks, and great numbers are drowned at sea whenever the weather is unfavourable. Some individuals always stay through the winter in the south of Europe, and a few even in England and Ireland; and were the sea to become a little wider the migration would cease, and the quail, like some other birds, would remain divided between south Europe and north Africa. Aquatic birds are observed to follow the routes of great rivers and lakes, and the shores of the sea. One great body reaches central Europe by way of the Danube from the shores of the Black Sea; another ascends the Rhone Valley from the Gulf of Lyons. {23}_India and China._--In the peninsula of India and in China great numbers of northern birds arrive during September and October, and leave from March to May. Among the smaller birds are wagtails, pipits, larks, stonechats, warblers, thrushes, buntings, shrikes, starlings, hoopoes, and quails. Some species of cranes and storks, many ducks, and great numbers of _Scolopacidæ_ also visit India in winter; and to prey upon these come a band of rapacious birds--the peregrine falcon, the hobby, kestrel, common sparrowhawk, harrier, and the short-eared owl. These birds are almost all natives of Europe and Western Asia; they spread over all northern and central India, mingling with the sedentary birds of the oriental fauna, and give to the ornithology of Hindostan at this season quite a European aspect. The peculiar species of the higher Himalayas do not as a rule descend to the plains in winter, but merely come lower down the mountains; and in southern India and Ceylon comparatively few of these migratory birds appear. In China the migratory birds follow generally the coast line, coming southwards in winter from eastern Siberia and northern Japan; while a few purely tropical forms travel northwards in summer to Japan, and on the mainland as far as the valley of the Amoor. _North America._--The migrations of birds in North America have been carefully studied by resident naturalists, and present some interesting features. The birds of the eastern parts of North America are pre-eminently migratory, a much smaller proportion being permanent residents than in corresponding latitudes in Europe. Thus, in Massachusetts there are only about 30 species of birds which are resident all the year, while the regular summer visitors are 106. Comparing with this our own country, though considerably further north, the proportions are reversed; there being 140 residents and 63 summer visitors. This difference is clearly due to the much greater length and severity of the winter, and the greater heat of summer, in America than with us. The number of permanent residents increases pretty regularly as we go southward; but the number of birds at any locality during the breeding season seems to increase as we go {24}northward as far as Canada, where, according to Mr. Allen, more species breed than in the warm Southern States. Even in the extreme north, beyond the limit of forests, there are no less than 60 species which breed; in Canada about 160; while in Carolina there are only 135, and in Louisiana, 130. The extent of the migration varies greatly, some species only going a few degrees north and south, while others migrate annually from the tropics to the extreme north of the continent; and every gradation occurs between these extremes. Among those which migrate furthest are the species of _Dendroeca_, and other American flycatching warblers (_Mniotiltidæ_), many of which breed on the shores of Hudson's Bay, and spend the winter in Mexico or the West Indian islands. The great migratory movement of American birds is almost wholly confined to the east coast; the birds of the high central plains and of California being for the most part sedentary, or only migrating for short distances. All the species which reach South America, and most of those which winter in Mexico and Guatemala, are exclusively eastern species; though a few Rocky Mountain birds range southward along the plateaux of Mexico and Guatemala, but probably not as regular annual migrants. In America as in Europe birds appear in spring with great regularity, while the time of the autumnal return is less constant. More curious is the fact, also observed in both hemispheres, that they do not all return by the same route followed in going northwards, some species being constant visitors to certain localities in spring but not in autumn, others in autumn but not in spring. Some interesting cases have been observed in America of a gradual alteration in the extent of the migration of certain birds. A Mexican swallow (_Hirundo lunifrons_) first appeared in Ohio in 1815. Year by year it increased the extent of its range till by 1845 it had reached Maine and Canada; and it is now quoted by American writers as extending its annual migrations to Hudson's Bay. An American wren (_Troglodytes ludovicianus_) is another bird which has spread considerably northwards since {25}the time of the ornithologist Wilson; and the rice-bird, or "Bob-o'-link," of the Americans, continually widens its range as rice and wheat are more extensively cultivated. This bird winters in Cuba and other West Indian Islands, and probably also in Mexico. In April it enters the Southern States and passes northward, till in June it reaches Canada and extends west to the Saskatchewan River in 54° north latitude. _South Temperate America._--The migratory birds of this part of the world have been observed by Mr. Hudson at Buenos Ayres. As in Europe and North America, there are winter and summer visitors, from Patagonia and the tropics respectively. Species of _Pyrocephalus_, _Milvulus_, swallows, and a hummingbird, are among the most regular of the summer visitors. They are all insectivorous birds. From Patagonia species of _Tænioptera_, _Cinclodes_, and _Centrites_, come in winter, with two gulls, two geese, and six snipes and plovers. Five species of swallows appear at Buenos Ayres in spring, some staying to breed, others passing on to more temperate regions farther south. As a rule the birds which come late and leave early are the most regular. Some are very irregular in their movements, the _Molothrus bonariensis_, for example, sometimes leaves early in autumn, sometimes remains all the winter. Some resident birds also move in winter to districts where they are never seen in summer. _General Remarks on Migration._--The preceding summary of the main facts of migration (which might have been almost indefinitely extended, owing to the great mass of detailed information that exists on the subject) appears to accord with the view already suggested, that the "instinct" of migration has arisen from the habit of wandering in search of food common to all animals, but greatly exaggerated in the case of birds by their powers of flight and by the necessity for procuring a large amount of soft insect food for their unfledged young. Migration in its simple form may be best studied in North America, where it takes place over a continuous land surface with a considerable change of climate from south to north. We have here (as probably in Europe and elsewhere) every grade of migration, from species which merely shift the northern and southern {26}limits of their range a few hundred miles, so that in the central parts of the area the species is a permanent resident, to others which move completely over 1,000 miles of latitude, so that in all the intervening districts they are only known as birds of passage. Now, just as the rice-bird and the Mexican swallow have extended their migrations, owing to favourable conditions induced by human agency; so we may presume that large numbers of species would extend their range where favourable conditions arose through natural causes. If we go back only as far as the height of the glacial epoch, there is reason to believe that all North America, as far south as about 40° north latitude, was covered with an almost continuous and perennial ice-sheet. At this time the migratory birds would extend up to this barrier (which would probably terminate in the midst of luxuriant vegetation, just as the glaciers of Switzerland now often terminate amid forests and corn-fields), and as the cold decreased and the ice retired almost imperceptibly year by year, would follow it up farther and farther according as the peculiarities of vegetation and insect-food were more or less suited to their several constitutions. It is an ascertained fact that many individual birds return year after year to build their nests in the same spot. This shows a strong local attachment, and is, in fact, the faculty or feeling on which their very existence probably depends. For were they to wander at random each year, they would almost certainly not meet with places so well suited to them, and might even get into districts where they or their young would inevitably perish. It is also a curious fact that in so many cases the old birds migrate first, leaving the young ones behind, who follow some short time later, but do not go so far as their parents. This is very strongly opposed to the notion of an imperative instinct. The old birds have been before, the young have not; and it is only when the old ones have all or nearly all gone that the young go too, probably following some of the latest stragglers. They wander, however, almost at random, and the majority are destroyed before the next spring. This is proved by the fact that the birds which return in spring are as a rule not more numerous than those which came the {27}preceding spring, whereas those which went away in autumn were two or three times as numerous. Those young birds that do get back, however, have learnt by experience, and the next year they take care to go with the old ones. The most striking fact in favour of the "instinct" of migration is the "agitation," or excitement, of confined birds at the time when their wild companions are migrating. It seems probable, however, that this is what may be called a social excitement, due to the anxious cries of the migrating birds; a view supported by the fact stated by Marcel de Serres, that the black swan of Australia, when domesticated in Europe, sometimes joins wild swans in their northward migration. We must remember too that migration at the proper time is in many cases absolutely essential to the existence of the species; and it is therefore not improbable that some strong social emotion should have been gradually developed in the race, by the circumstance that all who for want of such emotion did not join their fellows inevitably perished. The mode by which a passage originally overland has been converted into one over the sea offers no insuperable difficulties, as has already been pointed out. The long flights of some birds without apparently stopping on the way is thought to be inexplicable, as well as their finding their nesting-place of the previous year from a distance of many hundreds or even a thousand miles. But the observant powers of animals are very great; and birds flying high in the air may be guided by the physical features of the country spread out beneath them in a way that would be impracticable to purely terrestrial animals. It is assumed by some writers that the breeding-place of a species is to be considered as its true home rather than that to which it retires in winter; but this can hardly be accepted as a rule of universal application. A bird can only breed successfully where it can find sufficient food for its young; and the reason probably why so many of the smaller birds leave the warm southern regions to breed in temperate or even cold latitudes, is because caterpillars and other soft insect larvæ are there abundant at the proper time, while in their winter home the {28}larvæ have all changed into winged insects. But this favourable breeding district will change its position with change of climate; and as the last great change has been one of increased warmth in all the temperate zones, it is probable that many of the migratory birds are comparatively recent visitors. Other changes may however have taken place, affecting the vegetation and consequently the insects of a district; and we have seldom the means of determining in any particular case in what direction the last extension of range occurred. For the purposes of the study of geographical distribution therefore, we must, except in special cases, consider the true range of a species to comprise all the area which it occupies regularly for any part of the year, while all those districts which it only visits at more or less distant intervals, apparently driven by storms or by hunger, and where it never regularly or permanently settles, should not be included as forming part of its area of distribution. _Means of Dispersal of Reptiles and Amphibia._--If we leave out of consideration the true marine groups--the turtles and sea-snakes--reptiles are scarcely more fitted for traversing seas and oceans than are mammalia. We accordingly find that in those oceanic islands which possess no indigenous mammals, land reptiles are also generally wanting. The several groups of these animals, however, differ considerably both in their means of dispersal and in their power of resisting adverse conditions. Snakes are most dependent on climate, becoming very scarce in temperate and cold climates and entirely ceasing at 62° north latitude, and they do not ascend very lofty mountains, ceasing at 6,000 feet elevation in the Alps. Some inhabit deserts, others swamps and marshes, while many are adapted for a life in forests. They swim rivers easily, but apparently have no means of passing the sea, since they are very rarely found on oceanic islands. Lizards are also essentially tropical, but they go somewhat farther north than snakes, and ascend higher on the mountains, reaching 10,000 feet in the Alps. They possess too some unknown means (probably in the egg-state) of passing over the ocean, since they are found to inhabit many islands where there are neither mammalia nor snakes. {29}The amphibia are much less sensitive to cold than are true reptiles, and they accordingly extend much farther north, frogs being found within the arctic circle. Their semi-aquatic life also gives them facilities for dispersal, and their eggs are no doubt sometimes carried by aquatic birds from one pond or stream to another. Salt water is fatal to them as well as to their eggs, and hence it arises that they are seldom found in those oceanic islands from which mammalia are absent. Deserts and oceans would probably form the most effectual barriers to their dispersal; whereas both snakes and lizards abound in deserts, and have some means of occasionally passing the ocean which frogs and salamanders do not seem to possess. _Means of Dispersal of Fishes._--The fact that the same species of freshwater fish often inhabit distinct river systems, proves that they have some means of dispersal over land. The many authentic accounts of fish falling from the atmosphere, indicate one of the means by which they may be transferred from one river basin to another, viz., by hurricanes and whirlwinds, which often carry up considerable quantities of water and with it fishes of small size. In volcanic countries, also, the fishes of subterranean streams may sometimes be thrown up by volcanic explosions, as Humboldt relates happened in South America. Another mode by which fishes may be distributed is by their eggs being occasionally carried away by aquatic birds; and it is stated by Gmelin that geese and ducks during their migrations feed on the eggs of fish, and that some of these pass through their bodies with their vitality unimpaired.[2] Even water-beetles flying from one pond to another might occasionally carry with them some of the smaller eggs of fishes. But it is probable that fresh-water fish are also enabled to migrate by changes of level causing streams to alter their course and carry their waters into adjacent basins. On plateaux the sources of distinct river systems often approach each other, and the same thing occurs with lateral tributaries on the lowlands near their mouths. Such changes, although small in extent, and occurring only at long intervals, would {30}act very powerfully in modifying the distribution of fresh-water fish. Sea fish would seem at first sight to have almost unlimited means of dispersal, but this is far from being the case. Temperature forms a complete barrier to a large number of species, cold water being essential to many, while others can only dwell in the warmth of the tropics. Deep water is another barrier to large numbers of species which are adapted to shores and shallows; and thus the Atlantic is quite as impassable a gulf to most fishes as it is to birds. Many sea fishes migrate to a limited extent for the purpose of depositing their spawn in favourable situations. The herring, an inhabitant of the deep sea, comes in shoals to our coast in the breeding season; while the salmon quits the northern seas and enters our rivers, mounting upwards to the clear cold water near their sources to deposit its eggs. Keeping in mind the essential fact that changes of temperature and of depth are the main barriers to the dispersal of fish, we shall find little difficulty in tracing the causes that have determined their distribution. _Means of Dispersal of Mollusca._--The marine, fresh-water, and land mollusca are three groups whose powers of dispersal and consequent distribution are very different, and must be separately considered. The _Pteropoda_, the _Ianthina_, and other groups of floating molluscs, drift about in mid-ocean, and their dispersal is probably limited chiefly by temperature, but perhaps also by the presence of enemies or the scarcity of proper food. The univalve and bivalve mollusca, of which the whelk and the cockle may be taken as types, move so slowly in their adult state, that we should expect them to have an exceedingly limited distribution; but the young of all these are free swimming embryos, and they thus have a powerful means of dispersal, and are carried by tides and currents so as ultimately to spread over every shore and shoal that offers conditions favourable for their development. The fresh water molluscs, which one might at first suppose could not range beyond their own river-basin, are yet very widely distributed in common with almost all other fresh water productions; and Mr. Darwin has shown that this is {31}due to the fact, that ponds and marshes are constantly frequented by wading and swimming birds which are pre-eminently wanderers, and which frequently carry away with them the seeds of plants, and the eggs of molluscs and aquatic insects. Fresh water molluscs just hatched were found to attach themselves to a duck's foot suspended in an aquarium; and they would thus be easily carried from one lake or river to another, and by the help of different species of aquatic birds, might soon spread all over the globe. Even a water-beetle has been caught with a small living shell (_Ancylus_) attached to it; and these fly long distances and are liable to be blown out to sea, one having been caught on board the _Beagle_ when forty-five miles from land. Although fresh water molluscs and their eggs must frequently be carried out to sea, yet this cannot lead to their dispersal, since salt water is almost immediately fatal to them; and we are therefore forced to conclude that the apparently insignificant and uncertain means of dispersal above alluded to are really what have led to their wide distribution. The true land-shells offer a still more difficult case, for they are exceedingly sensitive to the influence of salt water; they are not likely to be carried by aquatic birds, and yet they are more or less abundant all over the globe, inhabiting the most remote oceanic islands. It has been found, however, that land-shells have the power of lying dormant a long time. Some have lived two years and a half shut up in pill boxes; and one Egyptian desert snail came to life after having been glued down to a tablet in the British Museum for four years! We are indebted to Mr. Darwin for experiments on the power of land shells to resist sea water, and he found that when they had formed a membranous diaphragm over the mouth of the shell they survived many days' immersion (in one case fourteen days); and another experimenter, quoted by Mr. Darwin, found that out of one hundred land shells immersed for a fortnight in the sea, twenty-seven recovered. It is therefore quite possible for them to be carried in the chinks of drift wood for many hundred miles across the sea, and this is probably one of the most effectual modes of their dispersal. Very young shells would also {32}sometimes attach themselves to the feet of birds walking or resting on the ground, and as many of the waders often go far inland, this may have been one of the methods of distributing species of land shells; for it must always be remembered that nature can afford to wait, and that if but once in a thousand years a single bird should convey two or three minute snails to a distant island, this is all that is required for us to find that island well stocked with a great and varied population of land shells. _Means of Dispersal of Insects and the Barriers which Limit their Range._--Winged insects, as a whole, have perhaps more varied means of dispersal over the globe than any other highly organised animals. Many of them can fly immense distances, and the more delicate ones are liable to be carried by storms and hurricanes over a wide expanse of ocean. They are often met with far out at sea. Hawk-moths frequently fly on board ships as they approach the shores of tropical countries, and they have sometimes been captured more than 250 miles from the nearest land. Dragon-flies came on board the _Adventure_ frigate when fifty miles off the coast of South America. A southerly wind brought flies in myriads to Admiral Smyth's ship in the Mediterranean when he was 100 miles distant from the coast of Africa. A large Indian beetle (_Chrysochroa ocellata_) was quite recently caught alive in the Bay of Bengal by Captain Payne of the barque _William Mansoon_, 273 miles from the nearest land. Darwin caught a locust 370 miles from land; and in 1844 swarms of locusts several miles in extent, and as thick as the flakes in a heavy snowstorm, visited Madeira. These must have come with perfect safety more than 300 miles; and as they continued flying over the island for a long time, they could evidently have travelled to a much greater distance. Numbers of living beetles belonging to seven genera, some aquatic and some terrestrial, were caught by Mr. Darwin in the open sea, seventeen miles from the coast of South America, and they did not seem injured by the salt water. Almost all the accidental causes that lead to the dispersal of the higher animals would be still more favourable for insects. Floating trees could carry hundreds of insects for one bird or mammal; and so many of the larvæ, eggs, {33}and pupæ of insects have their abode in solid timber, that they might survive being floated immense distances. Great numbers of tropical insects have been captured in the London docks, where they have been brought in foreign timber; and some have emerged from furniture after remaining torpid for many years. Most insects have the power of existing weeks or months without food, and some are very tenacious of life. Many beetles will survive immersion for hours in strong spirit; and water a few degrees below the boiling point will not always kill them. We can therefore easily understand how, in the course of ages insects may become dispersed by means which would be quite inadequate in the case of the higher animals. The drift-wood and tropical fruits that reach Ireland and the Orkneys; the double cocoa-nuts that cross the Indian ocean from the Seychelle Islands to the coast of Sumatra; the winds that carry volcanic dust and ashes for thousands of miles; the hurricanes that travel in their revolving course over wide oceans; all indicate means by which a few insects may, at rare intervals be carried to remote regions, and become the progenitors of a group of allied forms. But the dispersal of insects requires to be looked at from another point of view. They are, of all animals, perhaps the most wonderfully adapted for special conditions; and are so often fitted to fill one place in nature and one only, that the barriers against their permanent displacement are almost as numerous and as effective as their means of dispersal. Hundreds of species of lepidoptera, for example, can subsist in the larva state only on one species of plant; so that even if the perfect insects were carried to a new country, the continuance of the race would depend upon the same or a closely allied plant being abundant there. Other insects require succulent vegetable food all the year round, and are therefore confined to tropical regions; some can live only in deserts, others in forests; some are dependent on water-plants, some on mountain-vegetation. Many are so intimately connected with other insects during some part of their existence that they could not live without them; such are the parasitical hymenoptera and diptera, and those mimicking species whose welfare depends upon their being {34}mistaken for something else. Then again, insects have enemies in every stage of their existence--the egg, the larva, the pupa, and the perfect form; and the abundance of any one of these enemies may render their survival impossible in a country otherwise well suited to them. Ever bearing in mind these two opposing classes of facts, we shall not be surprised at the enormous range of some groups of insects, and at the extreme localization of others; and shall be able to give a rational account of many phenomena of distribution that would otherwise seem quite unintelligible. {35}CHAPTER III. DISTRIBUTION AS AFFECTED BY THE CONDITIONS AND CHANGES OF THE EARTH'S SURFACE. The distribution of animals over the earth's surface, is evidently dependent in great measure upon those grand and important characteristics of our globe, the study of which is termed physical geography. The proportion of land and water; the outlines and distribution of continents; the depth of seas and oceans; the position of islands; the height, direction, and continuity of mountain chains; the position and extent of deserts, lakes, and forests; the direction and velocity of ocean currents, as well as of prevalent winds and hurricanes; and lastly, the distribution of heat and cold, of rain, snow, and ice, both in their means and in their extremes, have all to be considered when we endeavour to account for the often unequal and unsymmetrical manner in which animals are dispersed over the globe. But even this knowledge is insufficient unless we inquire further as to the evidence of permanence possessed by each of these features, in order that we may give due weight to the various causes that have led to the existing facts of animal distribution. _Land and Water._--The well-known fact that nearly three-fourths of the surface of the earth is occupied by water, and but a little more than one-fourth by land, is important as indicating the vast extent of ocean by which many of the continents and islands are separated from each other. But there is another fact {36}which greatly increases its importance, namely, that the mean height of the land is very small compared with the mean depth of the sea. It has been estimated by Humboldt that the mean height of all the land surface does not exceed a thousand feet, owing to the comparative narrowness of mountain ranges and the great extent of alluvial plains and valleys; the ocean bed, on the contrary, not only descends deeper than the tops of the highest mountains rise above its surface, but these profound depths are broad sunken plains, while the shallows correspond to the mountain ranges, so that its mean depth is, as nearly as can be estimated, twelve thousand feet.[3] Hence, as the area of water is three times that of the land, the total cubical contents of the land, above the sea level, would be only that of the waters which are below that level. The important result follows, that whereas it is scarcely possible that in past times the amount of land surface should ever greatly have exceeded that which now exists, it is just possible that all the land may have been at some time submerged; and therefore in the highest degree probable that among the continual changes of land and sea that have been always going on, the amount of land surface has often been much less than it is now. For the same reason it is probable that there have been times when large masses of land have been more isolated from the rest than they are at present; just as South America would be if North America were submerged, or as Australia would become if the Malay Archipelago were to sink beneath the ocean. It is also very important to bear in mind the fact insisted on by Sir Charles Lyell, that the shallow parts of the ocean are almost always in the vicinity of land; and that an amount of elevation that would make little difference to the bed of the ocean, would raise up extensive tracts of dry land in the vicinity of existing continents. It is almost certain, therefore, that changes in the distribution of land and sea must have taken place more frequently by additions to, or {37}modifications of pre-existing land, than by the upheaval of entirely new continents in mid-ocean. These two principles will throw light upon two constantly recurring groups of facts in the distribution of animals,--the restriction of peculiar forms to areas not at present isolated,--and on the other hand, the occurrence of allied forms in lands situated on opposite shores of the great oceans. _Continental Areas._--Although the dry land of the earth's surface is distributed with so much irregularity, that there is more than twice as much north of the equator as there is south of it, and about twice as much in the Asiatic as in the American hemisphere; and, what is still more extraordinary, that on a hemisphere of which a point in St. George's Channel between England and Ireland is the centre, the land is nearly equal in extent to the water, while in the opposite hemisphere it is in the proportion of only one-eighth,--yet the whole of the land is almost continuous. It consists essentially of only three masses: the American, the Asia-African, and the Australian. The two former are only separated by thirty-six miles of shallow sea at Behring's Straits, so that it is possible to go from Cape Horn to Singapore or the Cape of Good Hope without ever being out of sight of land; and owing to the intervention of the numerous islands of the Malay Archipelago the journey might be continued under the same conditions as far as Melbourne and Hobart Town. This curious fact, of the almost perfect continuity of all the great masses of land notwithstanding their extremely irregular shape and distribution, is no doubt dependent on the circumstances just alluded to; that the great depth of the oceans and the slowness of the process of upheaval, has almost always produced the new lands either close to, or actually connected with pre-existing lands; and this has necessarily led to a much greater uniformity in the distribution of organic forms, than would have prevailed had the continents been more completely isolated from each other. The isthmuses which connect Africa with Asia, and North with South America, are, however, so small and insignificant compared with the vast extent of the countries they unite that {38}we can hardly consider them to form more than a nominal connection. The Isthmus of Suez indeed, being itself a desert, and connecting districts which for a great distance are more or less desert also, does not effect any real union between the luxuriant forest-clad regions of intertropical Asia and Africa. The Isthmus of Panama is a more effectual line of union, since it is hilly, well watered, and covered with luxuriant vegetation; and we accordingly find that the main features of South American zoology are continued into Central America and Mexico. In Asia a great transverse barrier exists, dividing that continent into a northern and southern portion; and as the lowlands occur on the south and the highlands on the north of the great mountain range, which is situated not far beyond the tropic, an abrupt change of climate is produced; so that a belt of about a hundred miles wide, is all that intervenes between a luxuriant tropical region and an almost arctic waste. Between the northern part of Asia, and Europe, there is no barrier of importance; and it is impossible to separate these regions as regards the main features of animal life. Africa, like Asia, has a great transverse barrier, but it is a desert instead of a mountain chain; and it is found that this desert is a more effectual barrier to the diffusion of animals than the Mediterranean Sea; partly because it coincides with the natural division of a tropical from a temperate climate, but also on account of recent geological changes which we shall presently allude to. It results then from this outline sketch of the earth's surface, that the primary divisions of the geographer correspond approximately with those of the zoologist. Some large portion of each of the popular divisions forms the nucleus of a zoological region; but the boundaries are so changed that the geographer would hardly recognise them: it has, therefore, been found necessary to give them those distinct names which will be fully explained in our next chapter. _Recent Changes in the Continental Areas._--The important fact has been now ascertained, that a considerable portion of the Sahara south of Algeria and Morocco was under water at a very recent epoch. Over much of this area sea-shells, identical with those now living in the Mediterranean, are abundantly scattered, {39}not only in depressions below the level of the sea but up to a height of 900 feet above it. Borings for water made by the French government have shown, that these shells occur twenty feet deep in the sand; and the occurrence of abundance of salt, sometimes even forming considerable hills, is an additional proof of the disappearance of a large body of salt water. The common cockle is one of the most abundant of the shells found; and the Rev. H. B. Tristram discovered a new fish, in a salt lake nearly 300 miles inland, but which has since been found to inhabit the Gulf of Guinea. Connected with this proof of recent elevation in the Sahara, we have most interesting indications of subsidence in the area of the Mediterranean, which were perhaps contemporaneous. Sicily and Malta are connected with Africa by a submerged bank from 300 to 1,200 feet below the surface; while the depth of the Mediterranean, both to the east and west, is enormous, in some parts more than 13,000 feet; and another submerged bank with a depth of 1,000 feet occurs at the straits of Gibraltar. In caves in Sicily, remains of the living African elephant have been found by Baron Anca; and in other caves Dr. Falconer discovered remains of the _Elephas antiquus_ and of two species of _Hippopotamus_. In Malta, three species of elephant have been discovered by Captain Spratt; a large one closely allied to _E. antiquus_ and two smaller ones not exceeding five feet high when adult. These facts clearly indicate, that when North Africa was separated by a broad arm of the sea from the rest of the continent, it was probably connected with Europe; and this explains why zoologists find themselves obliged to place it along with Europe in the same zoological region. Besides this change in the level of the Sahara and the Mediterranean basin, Europe has undergone many fluctuations in its physical geography in very recent times. In Wales, abundance of sea-shells of living species have been found at an elevation of 1,300 feet; and in Sardinia there is proof of an elevation of 300 feet since the human epoch; and these are only samples of many such changes of level. But these changes, though very important locally and as connected with geological problems, need not be further noticed here; as they were not of a {40}nature to affect the larger features of the earth's surface or to determine the boundaries of great zoological regions. The only other recent change of great importance which can be adduced to illustrate our present subject, is that which has taken place between North and South America. The living marine shells of the opposite coasts of the isthmus of Panama, as well as the corals and fishes, are generally of distinct species, but some are identical and many are closely allied; the West Indian fossil shells and corals of the Miocene period, however, are found to be largely identical with those of the Pacific coast. The fishes of the Atlantic and Pacific shores of America are as a rule very distinct; but Dr. Günther has recently shown that a considerable number of species inhabiting the seas on opposite sides of the isthmus are absolutely identical. These facts certainly indicate, that during the Miocene epoch a broad channel separated North and South America; and it seems probable that a series of elevations and subsidences have taken place uniting and separating them at different epochs; the most recent submersion having lasted but a short time, and thus, while allowing the passage of abundance of locomotive fishes, not admitting of much change in the comparatively stationary mollusca. _The Glacial Epoch as affecting the Distribution of Animals._--The remarkable refrigeration of climate in the northern hemisphere within the epoch, of existing species, to which the term Glacial epoch is applied, together with the changes of level that accompanied and perhaps assisted to produce it, has been one of the chief agents in determining many of the details of the existing distribution of animals in temperate zones. A comparison of the effects produced by existing glaciers with certain superficial phenomena in the temperate parts of Europe and North America, renders it certain that between the Newer Pliocene and the Recent epochs, a large portion of the northern hemisphere must have been covered with a sheet of ice several thousand feet thick, like that which now envelopes the interior of Greenland. Much further south the mountains were covered with perpetual snow, and sent glaciers down every valley; and all the {41}great valleys on the southern side of the Alps poured down streams of ice which stretched far out into the plains of Northern Italy, and have left their débris in the form of huge mountainous moraines, in some cases more than a thousand feet high. In Canada and New Hampshire the marks of moving ice are found on the tops of mountains from 3,000 to 5,000 feet high; and the whole surface of the country around and to the north of the great lakes is scored by glaciers. Wherever the land was submerged during a part of this cold period, a deposit called boulder-clay, or glacial-drift has been formed. This is a mass of sand, clay, or gravel, full of angular or rounded stones of all sizes, up to huge blocks as large as a cottage; and especially characterized by these stones being distributed confusedly through it, the largest being as often near the top as near the bottom, and never sorted into layers of different sizes as in materials carried by water. Such deposits are known to be formed by glaciers and icebergs; when deposited on the land by glaciers they form moraines, when carried into water and thus spread with more regularity over a wider area they form drift. This drift is rarely found except where there is other evidence of ice-action, and never south of the 40th parallel of latitude, to which in the northern hemisphere signs of ice-action extend. In the southern hemisphere, in Patagonia and in New Zealand, exactly similar phenomena occur. A very interesting confirmation of the reality of this cold epoch is derived from the study of fossil remains. Both the plants and animals of the Miocene period indicate that the climate of Central Europe was decidedly warmer or more equable than it is now; since the flora closely resembled that of the Southern United States, with a likeness also to that of Eastern Asia and Australia. Many of the shells were of tropical genera; and there were numbers of large mammalia allied to the elephant, rhinoceros, and tapir. At the same time, or perhaps somewhat earlier, a temperate climate extended into the arctic regions, and allowed a magnificent vegetation of shrubs and forest trees, some of them evergreen, to flourish within twelve degrees of the Pole. In the Pliocene period we find ourselves {42}among forms implying a climate very little different from the present; and our own Crag formation furnishes evidence of a gradual refrigeration of climate; since its three divisions, the Coralline, Red, and Norwich Crags, show a decreasing number of southern, and an increasing number of northern species, as we approach the Glacial epoch. Still later than these we have the shells of the drift, almost all of which are northern and many of them arctic species. Among the mammalia indicative of cold, are the mammoth and the reindeer. In gravels and cave-deposits of Post-Pliocene date we find the same two animals, which soon disappear as the climate approached its present condition; and Professor Forbes has given a list of fifty shells which inhabited the British seas before the Glacial epoch and inhabit it still, but are all wanting in the glacial deposits. The whole of these are found in the Newer Pliocene strata of Sicily and the south of Europe, where they escaped destruction during the glacial winter. There are also certain facts in the distribution of plants, which are so well explained by the Glacial epoch that they may be said to give an additional confirmation to it. All over the northern hemisphere within the glaciated districts, the summits of lofty mountains produce plants identical with those of the polar regions. In the celebrated case of the White Mountains in New Hampshire, United States (latitude 45°), all the plants on the summit are arctic species, none of which exist in the lowlands for near a thousand miles further north. It has also been remarked that the plants of each mountain are more especially related to those of the countries directly north of it. Thus, those of the Pyrenees and of Scotland are Scandinavian, and those of the White Mountains are all species found in Labrador. Now, remembering that we have evidence of an exceedingly mild and uniform climate in the arctic regions during the Miocene period and a gradual refrigeration from that time, it is evident that with each degree of change more and more hardy plants would be successively driven southwards; till at last the plains of the temperate zone would be inhabited by plants, which were once confined to alpine heights or to the arctic regions. {43}As the icy mantle gradually melted off the face of the earth these plants would occupy the newly exposed soil, and would thus necessarily travel in two directions, back towards the arctic circle and up towards the alpine peaks. The facts are thus exactly explained by a cause which independent evidence has proved to be a real one, and every such explanation is an additional proof of the reality of the cause. But this explanation implies, that in cases where the Glacial epoch cannot have so acted alpine plants should not be northern plants; and a striking proof of this is to be found on the Peak of Teneriffe, a mountain 12,000 feet high. In the uppermost 4,500 feet of this mountain above the limit of trees, Von Buch found only eleven species of plants, eight of which were peculiar; but the whole were allied to those found at lower elevations. On the Alps or Pyrenees at this elevation, there would be a rich flora comprising hundreds of arctic plants; and the absence of anything corresponding to them in this case, in which their ingress was cut off by the sea, is exactly what the theory leads us to expect. _Changes of Vegetation as affecting the Distribution of Animals._--As so many animals are dependent on vegetation, its changes immediately affect their distribution. A remarkable example of this is afforded by the pre-historic condition of Denmark, as interpreted by means of the peat-bogs and kitchen-middens. This country is now celebrated for its beech-trees; oaks and pines being scarce; and it is known to have had the same vegetation in the time of the Romans. In the peat-bogs, however, are found deposits of oak trees; and deeper still pines alone occur. Now the kitchen-middens tell us much of the natural history of Denmark in the early Stone period; and a curious confirmation of the fact that Denmark like Norway was then chiefly covered with pine forests is obtained by the discovery, that the Capercailzie was then abundant, a bird which feeds almost exclusively on the young shoots and seeds of pines and allied plants. The cause of this change in the vegetation is unknown; but from the known fact that when forests are destroyed trees, of a different kind usually occupy the ground, we may suppose that some such change as a temporary submergence might cause an entirely {44}different vegetation and a considerably modified fauna to occupy the country. _Organic Changes as affecting Distribution._--We have now briefly touched on some of the direct effects of changes in physical geography, climate, and vegetation, on the distribution of animals; but the indirect effects of such changes are probably of quite equal, if not of greater importance. Every change becomes the centre of an ever-widening circle of effects. The different members of the organic world are so bound together by complex relations, that any one change generally involves numerous other changes, often of the most unexpected kind. We know comparatively little of the way in which one animal or plant is bound up with others, but we know enough to assure us that groups the most apparently disconnected are often dependent on each other. We know, for example, that the introduction of goats into St. Helena utterly destroyed a whole flora of forest trees; and with them all the insects, mollusca, and perhaps birds directly or indirectly dependent on them. Swine, which ran wild in Mauritius, exterminated the Dodo. The same animals are known to be the greatest enemies of venomous serpents. Cattle will, in many districts, wholly prevent the growth of trees; and with the trees the numerous insects dependent on those trees, and the birds which fed upon the insects, must disappear, as well as the small mammalia which feed on the fruits, seeds, leaves, or roots. Insects again have the most wonderful influence on the range of mammalia. In Paraguay a certain species of fly abounds which destroys new-born cattle and horses; and thus neither of these animals have run wild in that country, although they abound both north and south of it. This inevitably leads to a great difference in the vegetation of Paraguay, and through that to a difference in its insects, birds, reptiles, and wild mammalia. On what causes the existence of the fly depends we do not know, but it is not improbable that some comparatively slight changes in the temperature or humidity of the air at a particular season, or the introduction of some enemy might lead to its extinction or banishment. The whole face of the country would then soon be changed: new species would {45}come in, while many others would be unable to live there; and the immediate cause of this great alteration would probably be quite imperceptible to us, even if we could watch it in progress year by year. So, in South Africa, the celebrated Tsetse fly inhabits certain districts having well defined limits; and where it abounds no horses, dogs, or cattle can live. Yet asses, zebras, and antelopes are unaffected by it. So long as this fly continues to exist, there is a living barrier to the entrance of certain animals, quite as effectual as a lofty mountain range or a wide arm of the sea. The complex relations of one form of life with others is nowhere better illustrated than in Mr. Darwin's celebrated case of the cats and clover, as given in his _Origin of Species_, 6th ed., p. 57. He has observed that both wild heartsease and red-clover are fertilized in this country by humble-bees only, so that the production of seed depends on the visits of these insects. A gentleman who has specially studied humble-bees finds that they are largely kept down by field-mice, which destroy their combs and nests. Field-mice in their turn are kept down by cats; and probably also by owls; so that these carnivorous animals are really the agents in rendering possible the continued existence of red-clover and wild heartsease. For if they were absent, the field-mice having no enemies, would multiply to such an extent as to destroy all the humble-bees; and these two plants would then produce no seed and soon become extinct. Mr. Darwin has also shown that one species often exterminates another closely allied to it, when the two are brought into contact. One species of swallow and thrush are known to have increased at the expense of allied species. Rats, carried all over the world by commerce, are continually extirpating other species of rats. The imported hive-bee is, in Australia, rapidly exterminating a native stingless bee. Any slight change, therefore, of physical geography or of climate, which allows allied species hitherto inhabiting distinct areas to come into contact, will often lead to the extermination of one of them; and this extermination will be effected by no external force, by no actual enemy, but merely because the one is slightly better {46}adapted to live, to increase, and to maintain itself under adverse circumstances, than the other. Now if we consider carefully the few suggestive facts here referred to (and many others of like import are to be found in Mr. Darwin's various works), we shall be led to conclude that the several species, genera, families, and orders, both of animals and vegetables which inhabit any extensive region, are bound together by a series of complex relations; so that the increase, diminution, or extermination of any one, may set in motion a series of actions and reactions more or less affecting a large portion of the whole, and requiring perhaps centuries of fluctuation before the balance is restored. The range of any species or group in such a region, will in many cases (perhaps in most) be determined, not by physical barriers, but by the competition of other organisms. Where barriers have existed from a remote epoch, they will at first have kept back certain animals from coming in contact with each other; but when the assemblage of organisms on the two sides of the barrier have, after many ages, come to form a balanced organic whole, the destruction of the barrier may lead to a very partial intermingling of the peculiar forms of the two regions. Each will have become modified in special ways adapted to the organic and physical conditions of the country, and will form a living barrier to the entrance of animals less perfectly adapted to those conditions. Thus while the abolition of ancient barriers will always lead to much intermixture of forms, much extermination and wide-spread alteration in some families of animals; other important groups will be unable materially to alter their range; or they may make temporary incursions into the new territory, and be ultimately driven back to very near their ancient limits. In order to make this somewhat difficult subject more intelligible, it may be well to consider the probable effects of certain hypothetical conditions of the earth's surface:-- 1. If the dry land of the globe had been from the first continuous, and nowhere divided up by such boundaries as lofty mountain ranges, wide deserts, or arms of the sea, it seems probable that none of the larger groups (as _orders_, _tribes_, or {47}_families_,) would have a limited range; but, as is to some extent the case in tropical America east of the Andes, every such group would be represented over the whole area, by countless minute modifications of form adapted to local conditions. 2. One great physical barrier would, however, even then exist; the hot equatorial zone would divide the faunas and floras of the colder regions of the northern and southern hemispheres from any chance of intermixture. This one barrier would be more effectual than it is now, since there would be no lofty mountain ranges to serve as a bridge for the partial interchange of northern and southern forms. 3. If such a condition of the earth as here supposed continued for very long periods, we may conceive that the action and reaction of the various organisms on each other, combined with the influence of very slowly changing physical conditions, would result in an almost perfect organic balance, which would be manifested by a great stability in the average numbers, the local range, and the peculiar characteristics of every species. 4. Under such a condition of things it is not improbable that the total number of clearly differentiated specific forms might be much greater than it is now, though the number of generic and family types might perhaps be less; for dominant species would have had ample time to spread into every locality where they could exist, and would then become everywhere modified into forms best suited to the permanent local conditions. 5. Now let us consider what would be the probable effect of the introduction of a barrier, cutting off a portion of this homogeneous and well-balanced world. Suppose, for instance, that a subsidence took place, cutting off by a wide arm of the sea a large and tolerably varied island. The first and most obvious result would be that the individuals of a number of species would be divided into two portions, while others, the limits of whose range agreed approximately with the line of subsidence, would exist in unimpaired numbers on the new island or on the main land. But the species whose numbers were diminished and whose original area was also absolutely diminished by the portion now under the sea, would not be able to hold their {48}ground against the rival forms whose numbers were intact. Some would probably diminish and rapidly die out; others which produced favourable varieties, might be so modified by natural selection as to maintain their existence under a different form; and such changes would take place in varying modes on the two sides of the new strait. 6. But the progress of these changes would necessarily affect the other species in contact with them. New places would be opened in the economy of nature which many would struggle to obtain; and modification would go on in ever-widening circles and very long periods of time might be required to bring the whole again into a state of equilibrium. 7. A new set of factors would in the meantime have come into play. The sinking of land and the influx of a large body of water could hardly take place without producing important climatal changes. The temperature, the winds, the rains, might all be affected, and more or less changed in duration and amount. This would lead to a quite distinct movement in the organic world. Vegetation would certainly be considerably affected, and through this the insect tribes. We have seen how closely the life of the higher animals is often bound up with that of insects; and thus a set of changes might arise that would modify the numerical proportions, and even the forms and habits of a great number of species, would completely exterminate some, and raise others from a subordinate to a dominant position. And all these changes would occur differently on opposite sides of the strait, since the insular climate could not fail to differ considerably from that of the continent. 8. But the two sets of changes, as above indicated, produced by different modes of action of the same primary cause, would act and react on each other; and thus lead to such a far-spreading disturbance of the organic equilibrium as ultimately perhaps to affect in one way or another, every form of life upon the earth. This hypothetical case is useful as enabling us better to realize how wide-spreading might be the effects of one of the simplest changes of physical geography, upon a compact mass of mutually {49}adapted organisms. In the actual state of things, the physical changes that occur and have occurred through all geological epochs are larger and more varied. Almost every mile of land surface has been again and again depressed beneath the ocean; most of the great mountain chains have either originated or greatly increased in height during the Tertiary period; marvellous alterations of climate and vegetation have taken place over half the land-surface of the earth; and all these vast changes have influenced a globe so cut up by seas and oceans, by deserts and snow-clad mountains, that in many of its more isolated land-masses ancient forms of life have been preserved, which, in the more extensive and more varied continents have long given way to higher types. How complex then must have been the actions and reactions such a state of things would bring about; and how impossible must it be for us to guess, in most cases, at the exact nature of the forces that limit the range of some species and cause others to be rare or to become extinct! All that we can in general hope to do is, to trace out, more or less hypothetically, some of the larger changes in physical geography that have occurred during the ages immediately preceeding our own, and to estimate the effect they will probably have produced on animal distribution. We may then, by the aid of such knowledge as to past organic mutations as the geological record supplies us with, be able to determine the probable birthplace and subsequent migrations of the more important genera and families; and thus obtain some conception of that grand series of co-ordinated changes in the earth and its inhabitants, whose final result is seen in the forms and the geographical distribution of existing animals. {50}CHAPTER IV. ON ZOOLOGICAL REGIONS. To the older school of Naturalists the native country of an animal was of little importance, except in as far as climates differed. Animals were supposed to be specially adapted to live in certain zones or under certain physical conditions, and it was hardly recognised that apart from these conditions there was any influence in locality which could materially affect them. It was believed that, while the animals of tropical, temperate, and arctic climates, essentially differed; those of the tropics were essentially alike all over the world. A group of animals was said to inhabit the "Indies;" and important differences of structure were often overlooked from the idea, that creatures equally adapted to live in hot countries and with certain general resemblances, would naturally be related to each other. Thus the Toucans and Hornbills, the Humming-Birds and Sun-Birds, and even the Tapirs and the Elephants, came to be popularly associated as slightly modified varieties of tropical forms of life; while to naturalists, who were acquainted with the essential differences of structure, it was a never-failing source of surprise, that under climates and conditions so apparently identical, such strangely divergent forms should be produced. To the modern naturalist, on the other hand, the native country (or "habitat" as it is technically termed) of an animal {51}or a group of animals, is a matter of the first importance; and, as regards the general history of life upon the globe, may be considered to be one of its essential characters. The structure, affinities, and habits of a species, now form only a part of its natural history. We require also to know its exact range at the present day and in prehistoric times, and to have some knowledge of its geological age, the place of its earliest appearance on the globe, and of the various extinct forms most nearly allied to it. To those who accept the theory of development as worked out by Mr. Darwin, and the views as to the general permanence and immense antiquity of the great continents and oceans so ably developed by Sir Charles Lyell, it ceases to be a matter of surprise that the tropics of Africa, Asia, and America should differ in their productions, but rather that they should have anything in common. Their similarity, not their diversity, is the fact that most frequently puzzles us. The more accurate knowledge we have of late years obtained of the productions of many remote regions, combined with the greater approaches that have been made to a natural classification of the higher animals, has shown, that every continent or well-marked division of a continent, every archipelago and even every island, presents problems of more or less complexity to the student of the geographical distribution of animals. If we take up the subject from the zoological side, and study any family, order, or even extensive genus, we are almost sure to meet with some anomalies either in the present or past distribution of the various forms. Let us adduce a few examples of these problems. Deer have a wonderfully wide range, over the whole of Europe, Asia, and North and South America; yet in Africa south of the great desert there are none. Bears range over the whole of Europe, Asia, and North America, and true pigs of the genus Sus, over all Europe and Asia and as far as New Guinea; yet both bears and pigs, like deer, are absent from Tropical and South Africa. Again, the West Indian islands possess very few Mammalia, all of small size and allied to those of America, except one {52}genus; and that belongs to an Order, "Insectivora," entirely absent from South America, and to a family, "Centetidæ," all the other species of which inhabit Madagascar only. And as if to add force to this singular correspondence we have one Madagascar species of a beautiful day-flying Moth, _Urania_, all the other species of which inhabit tropical America. These insects are gorgeously arrayed in green and gold, and are quite unlike any other Lepidoptera upon the globe. The island of Ceylon generally agrees in its productions with the Southern part of India; yet it has several birds which are allied to Malayan and not to Indian groups, and a fine butterfly of the genus _Hestia_, as well as several genera of beetles, which are purely Malayan. Various important groups of animals are distributed in a way not easy to explain. The anthropoid apes in West Africa and Borneo; the tapirs in Malaya and South America; the camel tribe in the deserts of Asia and the Andes; the trogons in South America and Tropical Asia, with one species in Africa; the marsupials in Australia and America, are examples. The cases here adduced (and they might be greatly multiplied) are merely to show the kind of problems with which the naturalist now has to deal; and in order to do so he requires some system of geographical arrangement, which shall serve the double purpose of affording a convenient subdivision of his subject, and at the same time of giving expression to the main results at which he has arrived. Hence the recent discussions on "Zoological Regions," or, what are the most natural primary divisions of the earth as regards its forms of animal life. The divisions in use till quite recently were of two kinds; either those ready made by geographers, more especially the quarters or continents of the globe; or those determined by climate and marked out by certain parallels of latitude or by isothermal lines. Either of these methods was better than none at all; but from the various considerations explained in the preceding chapters, it will be evident, that such divisions must have often been very unnatural, and have disguised many {53}of the most important and interesting phenomena which a study of the distribution of animals presents to us. The merit of initiating a more natural system, that of determining zoological regions, not by any arbitrary or _a priori_ consideration but by studying the actual ranges of the more important groups of animals, is due to Mr. Sclater, who, in 1857, established six primary zoological regions from a detailed examination of the distribution of the chief genera and families of Birds. Before stating what these regions are, what objections have been made to them, what other divisions have been since proposed, and what are those which we shall adopt in this work, it will be well to consider the general principles which should guide us in the choice between rival systems. _Principles on which Zoological Regions should be formed._--It will be evident in the first place that nothing like a perfect zoological division of the earth is possible. The causes that have led to the present distribution of animal life are so varied, their action and reaction have been so complex, that anomalies and irregularities are sure to exist which will mar the symmetry of any rigid system. On two main points every system yet proposed, or that probably can be proposed, is open to objection; they are,--1stly, that the several regions are not of equal rank;--2ndly, that they are not equally applicable to all classes of animals. As to the first objection, it will be found impossible to form any three or more regions, each of which differs from the rest in an equal degree or in the same manner. One will surpass all others in the possession of peculiar families; another will have many characteristic genera; while a third will be mainly distinguished by negative characters. There will also be found many intermediate districts, which possess some of the characteristics of two well-marked regions, with a few special features of their own, or perhaps with none; and it will be a difficult question to decide in all cases which region should possess this doubtful territory, or whether it should be formed into a primary region itself. Again, two regions which have now well-marked points of difference, may be shown to have been much more alike at a comparatively recent geological epoch; {54}and this, it may be said, proves their fundamental unity and that they ought to form but one primary region. To obviate some of these difficulties a binary or dichotomous division is sometimes proposed; that portion of the earth which differs most from the rest being cut off as a region equal in rank to all that remains, which is subjected again and again to the same process. To decide these various points it seems advisable that convenience, intelligibility, and custom, should largely guide us. The first essential is, a broadly marked and easily remembered set of regions; which correspond, as nearly as truth to nature will allow, with the distribution of the most important groups of animals. What these groups are we shall presently explain. In determining the number, extent, and boundaries of these regions, we must be guided by a variety of indications, since the application of fixed rules is impossible. They should evidently be of a moderate number, corresponding as far as practicable with the great natural divisions of the globe marked out by nature, and which have always been recognized by geographers. There should be some approximation to equality of size, since there is reason to believe that a tolerably extensive area has been an essential condition for the development of most animal forms; and it is found that, other things being equal, the numbers, variety and importance of the forms of animal and vegetable life, do bear some approximate relation to extent of area. Although the possession of peculiar families or genera is the main character of a primary zoological region, yet the negative character of the absence of certain families or genera is of equal importance, _when this absence does not manifestly depend on unsuitability to the support of the group_, and especially _when there is now no physical barrier preventing their entrance_. This will become evident when we consider that the importance of the possession of a group by one region depends on its absence from the adjoining regions; and if there is now no barrier to its entrance, we may be sure that there has once been one; and that the possession of the area by a distinct and well balanced set of organisms, which must have been slowly {55}developed and adjusted, is the living barrier that now keeps out intruders. When it is ascertained that the chief differences which now obtain between two areas did not exist in Miocene or Pliocene times, the fact is one of great interest, and enables us to speculate with some degree of probability as to the causes that have brought about the present state of things; but it is not a reason for uniting these two areas into one region. Our object is to represent as nearly as possible the main features of the distribution of existing animals, not those of any or all past geological epochs. Should we ever obtain sufficient information as to the geography and biology of the earth at past epochs, we might indeed determine approximately what were the Pliocene or Miocene or Eocene zoological regions; but any attempt to exhibit all these in combination with those of our own period, must lead to confusion. The binary or dichotomous system, although it brings out the fundamental differences of the respective regions, is an inconvenient one in its application, and rather increases than obviates the difficulty as to equality or inequality of regions; for although _a_, _b_, _c_, and _d_, may be areas of unequal zoological rank, _a_ being the most important, and _d_ the least, yet this inequality will probably be still greater if we first divide them into _a_, on one side, and _b_, _c_, and _d_, on the other, and then, by another division, make _b_, an area of the second, and _c_, and _d_, of the third rank only. Coming to the second objection, the often incompatible distribution of different groups of animals, affords ground for opposition to any proposed scheme of zoological regions. There is first the radical difference between land and sea animals; the most complete barriers to the dispersal of the one, sometimes offering the greatest facilities for the emigration of the other, and _vice versa_. A large number of marine animals, however, frequent shallow water only; and these, keeping near the coasts, will agree generally in their distribution with those inhabiting the land. But among land animals themselves there are very great differences of distribution, due to certain specialities {56}in their organization or mode of life. These act mainly in two ways,--1stly, by affecting the facilities with which they can be dispersed, either voluntarily or involuntarily;--2ndly, by the conditions which enable them to multiply and establish themselves in certain areas and not in others. When both these means of diffusion are at a maximum, the dispersal of a group becomes universal, and ceases to have much interest for us. This is the case with certain groups of fungi and lichens, as well as with some of the lower animals; and in a less degree, as has been shown by Mr. Darwin, with many fresh-water plants and animals. At the other extreme we may place certain arboreal vertebrata such as sloths and lemurs, which have no means of passing such barriers as narrow straits or moderately high mountains, and whose survival in any new country they might reach, would be dependent on the presence of suitable forests and the absence of dangerous enemies. Almost equally, or perhaps even more restricted, are the means of permanent diffusion of terrestrial molluscs; since these are without any but very rare and accidental means of being safely transported across the sea; their individual powers of locomotion are highly restricted; they are especially subject to the attacks of enemies; and they often depend not only on a peculiar vegetation, but on the geological character of the country, their abundance being almost in direct proportion to the presence of some form of calcareous rocks. Between these extremes we find animals possessed of an infinite gradation of powers to disperse and to maintain themselves; and it will evidently be impossible that the limits which best define the distribution of one group, should be equally true for all others. _Which class of Animals is of most importance in determining Zoological Regions._--To decide this question we have to consider which groups of animals are best adapted to exhibit, by their existing distribution, the past changes and present physical condition of the earth's surface; and at the same time, by the abundance of their remains in the various tertiary formations will best enable us to trace out the more recent of the series of changes, both of the earth's surface and {57}of its inhabitants, by which the present state of things has been brought about. For this purpose we require a group which shall be dependent for its means of dispersal on the distribution of land and water, and on the presence or absence of lofty mountains, desert plains or plateaux, and great forests; since these are the chief physical features of the earth's surface whose modifications at successive periods we wish to discover. It is also essential that they should not be subject to dispersal by many accidental causes; as this would inevitably in time tend to obliterate the effect of natural barriers, and produce a scattered distribution, the causes of which we could only guess at. Again, it is necessary that they should be so highly organized as not to be absolutely dependent on other groups of animals, and with so much power of adaptation as to be able to exist in one form or another over the whole globe. And lastly, it is highly important that the whole group should be pretty well known, and that a fairly natural classification, especially of its minor divisions such as families and genera, should have been arrived at; the reason for which last proviso is explained in our next chapter, on classification. Now in every one of these points the mammalia are preeminent; and they possess the additional advantage of being the most highly developed class of organized beings, and that to which we ourselves belong. We should therefore construct our typical or standard Zoological Regions in the first place, from a consideration of the distribution of mammalia, only bringing to our aid the distribution of other groups to determine doubtful points. Regions so established will be most closely in accordance with those long-enduring features of physical geography, on which the distribution of all forms of life fundamentally depend; and all discrepancies in the distribution of other classes of animals must be capable of being explained, either by their exceptional means of dispersion or by special conditions affecting their perpetuation and increase in each locality. If these considerations are well founded, the objections of those who study insects or molluscs, for example,--that our regions are not true for their departments of nature--cannot be {58}maintained. For they will find, that a careful consideration of the exceptional means of dispersal and conditions of existence of each group, will explain most of the divergences from the normal distribution of higher animals. We shall thus be led to an intelligent comprehension of the phenomena of distribution in all groups, which would not be the case if every specialist formed regions for his own particular study. In many cases we should find that no satisfactory division of the earth could be made to correspond with the distribution even of an entire class; but we should have the coleopterist and the lepidopterist each with his own Geography. And even this would probably not suffice, for it is very doubtful if the detailed distribution of the Longicornes, so closely dependent on woody vegetation, could be made to agree with that of the Staphylinidæ or the Carabidæ which abound in many of the most barren regions, or with that of the Scarabeidæ, largely dependent on the presence of herbivorous mammalia. And when each of these enquirers had settled a division of the earth into "regions" which exhibited with tolerable accuracy the phenomena of distribution of his own group, we should have gained nothing whatever but a very complex mode of exhibiting the bare facts of distribution. We should then have to begin to work out the causes of the divergence of one group from another in this respect; but as each worker would refer to his own set of regions as the type, the whole subject would become involved in inextricable confusion. These considerations seem to make it imperative that one set of "regions" should be established as typical for Zoology; and it is hoped the reasons here advanced will satisfy most naturalists that these regions can be best determined, in the first place, by a study of the distribution of the mammalia, supplemented in doubtful cases by that of the other vertebrates. We will now proceed to a discussion of what these regions are. _Various Zoological Regions proposed since 1857._--It has already been pointed out that a very large number of birds are limited by the same kind of barriers as mammalia; it will therefore not be surprising that a system of regions formed to suit the {59}one, should very nearly represent the distribution of the other. Mr. Sclater's regions are as follows:-- 1. The Palæarctic Region; including Europe, Temperate Asia, and N. Africa to the Atlas mountains. 2. The Ethiopian Region; Africa south of the Atlas, Madagascar, and the Mascarene Islands, with Southern Arabia. 3. The Indian Region; including India south of the Himalayas, to South China, and to Borneo and Java. 4. The Australian Region; including Celebes and Lombock, eastward to Australia and the Pacific Islands. 5. The Nearctic Region; including Greenland, and N. America, to Northern Mexico. 6. The Neotropical Region; including South America, the Antilles, and Southern Mexico. This division of the earth received great support from Dr. Günther, who, in the _Proceedings of the Zoological Society_ for 1858, showed that the geographical distribution of Reptiles agreed with it very closely, the principal difference being that the reptiles of Japan have a more Indian character than the birds, this being especially the case with the snakes. In the volume for 1868 of the same work, Professor Huxley discusses at considerable length the primary and secondary zoological divisions of the earth. He gives reasons for thinking that the most radical primary division, both as regards birds and mammals, is into a Northern and Southern hemisphere (Arctogæa and Notogæa), the former, however, embracing all Africa, while the latter includes only Australasia and the Neotropical or Austro-Columbian region. Mr. Sclater had grouped his regions primarily into Palæogæa and Neogæa, the Old and New Worlds of geographers; a division which strikingly accords with the distribution of the passerine birds, but not so well with that of mammalia or reptiles. Professor Huxley points out that the Nearctic, Palæarctic, Indian, and Ethiopian regions of Mr. Sclater have a much greater resemblance to each other than any one of them has to Australia or to South America; and he further suggests that New Zealand alone has peculiarities which might entitle it to rank as a primary region {60}along with Australasia and South America; and that a Circumpolar Province might be conveniently recognised as of equal rank with the Palæarctic and Nearctic provinces. In 1866, Mr. Andrew Murray published a large and copiously illustrated volume on the _Geographical Distribution of Mammals_, in which he maintains that the great and primary mammalian regions are only four: 1st. The Palæarctic region of Mr. Sclater, extended to include the Sahara and Nubia; 2nd. the Indo-African region, including the Indian and Ethiopian regions of Mr. Sclater; 3rd. the Australian region (unaltered); 4th. the American region, including both North and South America. These are the regions as _described_ by Mr. Murray, but his coloured map of "Great Mammalian Regions" shows all Arctic America to a little south of the Isothermal of 32° Fahr. as forming with Europe and North Asia one great region. At the meeting of the British Association at Exeter in 1869, Mr. W. T. Blanford read a paper on the Fauna of British India, in which he maintained that a large portion of the peninsula of India had derived its Fauna mainly from Africa; and that the term "Indian region" of Mr. Sclater was misleading, because India proper, if it belongs to it at all, is the least typical portion of it. He therefore proposes to call it the "Malayan region," because in the Malay countries it is most highly developed. Ceylon and the mountain ranges of Southern India have marked Malay affinities. In 1871 Mr. E. Blyth published in _Nature_ "A suggested new Division of the Earth into Zoological Regions," in which he indicates seven primary divisions or regions, subdivided into twenty-six sub-regions. The seven regions are defined as follows: 1. The Boreal region; including the whole of the Palæarctic and Nearctic regions of Mr. Sclater along with the West Indies, Central America, the whole chain of the Andes, with Chili and Patagonia. 2. The Columbian region; consisting of the remaining part of South America. 3. The Ethiopian region; comprising besides that region of Mr. Sclater, the valley of the Jordan, Arabia, and the desert country towards India, with all the plains and table lands of India and the northern {61}half of Ceylon. 4. The Lemurian region; consisting of Madagascar and its adjacent islands. 5. The Austral-Asian region; which is the Indian region of Mr. Sclater without the portion taken to be added to the Ethiopian region. 6. The Melanesian region; which is the Australian region of Mr. Sclater without New Zealand and the Pacific Islands, which form 7. the Polynesian region. Mr. Blyth thinks this is "a true classification of zoological regions as regards mammalia and birds." In an elaborate paper on the birds of Eastern North America, their distribution and migrations (_Bulletin of Museum of Comparative Zoology, Cambridge, Massachusetts_, Vol. 2), Mr. J. A. Allen proposes a division of the earth in accordance with what he terms, "the law of circumpolar distribution of life in zones," as follows: 1. Arctic realm. 2. North temperate realm. 3. American tropical realm. 4. Indo-African tropical realm. 5. South American tropical realm. 6. African temperate realm. 7. Antarctic realm. 8. Australian realm. Some of these are subdivided into regions; (2) consisting of the American and the Europæo-Asiatic regions; (4) into the African and Indian regions; (8) into the tropical Australian region, and one comprising the southern part of Australia and New Zealand. The other realms each form a single region. _Discussion of proposed Regions._--Before proceeding to define the regions adopted in this work, it may be as well to make a few remarks on some of the preceding classifications, and to give the reasons which seem to render it advisable to adopt very few of the suggested improvements on Mr. Sclater's original proposal. Mr. Blyth's scheme is one of the least natural, and also the most inconvenient. There can be little use in the knowledge that a group of animals is found in the Boreal Region, if their habitat might still be either Patagonia, the West Indies, or Japan; and it is difficult to see on what principle the Madagascar group of islands is made of equal rank with this enormous region, seeing that its forms of life have marked African affinities. Neither does it seem advisable to adopt the Polynesian Region, or that comprising New Zealand alone (as hinted at by Professor Huxley and since adopted by {62}Mr. Sclater in his Lectures on Geographical Distribution at the Zoological Gardens in May 1874), because it is absolutely without indigenous mammalia and very poor in all forms of life, and therefore by no means prominent or important enough to form a primary region of the earth. It may be as well here to notice what appears to be a serious objection to making New Zealand, or any similar isolated district, one of the great zoological regions, comparable to South America, Australia, or Ethiopia; which is, that its claim to that distinction rests on grounds which are liable to fail. It is because New Zealand, in addition to its negative merits, possesses three families of birds (Apterygidæ living, Dinornithidæ and Palapterygidæ extinct), and a peculiar lizard-like reptile, _Hatteria_, which has to be classed in a distinct order, Rhynchocephalina, that the rank of a Region is claimed for it. But supposing, what is not at all improbable, that other Rhynchocephalina should be discovered in the interior of Australia or in New Guinea, and that Apterygidæ or Palapterygidæ should be found to have inhabited Australia in Post-Pliocene times, (as Dinornithidæ have already been proved to have done) the claims of New Zealand would entirely fail, and it would be universally acknowledged to be a part of the great Australian region. No such reversal can take place in the case of the other regions; because they rest, not upon one or two, but upon a large number of peculiarities, of such a nature that there is no room upon the globe for discoveries that can seriously modify them. Even if one or two peculiar types, like Apterygidæ or _Hatteria_, should permanently remain characteristic of New Zealand alone, we can account for these by the extreme isolation of the country, and the absence of enemies, which have enabled these defenceless birds and reptiles to continue their existence; just as the isolation and protection of the caverns of Carniola have enabled the _Proteus_ to survive in Europe. But supposing that the _Proteus_ was the sole representative of an order of Batrachia, and that two or three other equally curious and isolated forms occurred with it, no one would propose that these caverns or the district containing them, should form one of the {63}primary divisions of the earth. Neither can much stress be laid on the negative characteristics of New Zealand, since they are found to an almost equal extent in every oceanic island. Again, it is both inconvenient and misleading to pick out certain tracts from the midst of one region or sub-region and to place them in another, on account of certain isolated affinities which may often be accounted for by local peculiarities. Even if the resemblance of the fauna of Chili and Patagonia to that of the Palæarctic and Nearctic regions was much greater than it is, this mode of dealing with it would be objectionable; but it is still more so, when we find that these countries have a strongly marked South American character, and that the northern affinities are altogether exceptional. The Rodentia, which comprise a large portion of the mammalia of these countries, are wholly South American in type, and the birds are almost all allied to forms characteristic of tropical America. For analogous reasons the Ethiopian must not be made to include any part of India or Ceylon; for although the Fauna of Central India has some African affinities, these do not preponderate; and it will not be difficult to show that to follow Mr. Andrew Murray in uniting bodily the Ethiopian and Indian regions of Mr. Sclater, is both unnatural and inconvenient. The resemblances between them are of the same character as those which would unite them both with the Palæarctic and Nearctic regions; and although it may be admitted, that, as Professor Huxley maintains, this group forms one of the great primary divisions of the globe, it is far too extensive and too heterogeneous to subserve the practical uses for which we require a division of the world into zoological regions. _Reasons for adopting the six Regions first proposed by Mr. Sclater._--So that we do not violate any clear affinities or produce any glaring irregularities, it is a positive, and by no means an unimportant, advantage to have our named regions approximately equal in size, and with easily defined, and therefore easily remembered, boundaries. All elaborate definitions of interpenetrating frontiers, as well as regions extending over three-fourths of the land surface of the globe, and including places which are {64}the antipodes of each other, would be most inconvenient, even if there were not such difference of opinion about them. There can be little doubt, for example, that the most radical zoological division of the earth is made by separating the Australian region from the rest; but although it is something useful and definite to know that a group of animals is peculiar to Australia, it is exceedingly vague and unsatisfactory to say of any other group merely that it is extra-Australian. Neither can it be said that, from any point of view, these two divisions are of equal importance. The next great natural division that can be made is the separation of the Neotropical Region of Mr. Sclater from the rest of the world. We thus have three primary divisions, which Professor Huxley seems inclined to consider as of tolerably equal zoological importance. But a consideration of all the facts, zoological and palæontological, indicates, that the great northern division (Arctogæa) is fully as much more important than either Australia or South America, as its four component parts are less important; and if so, convenience requires us to adopt the smaller rather than the larger divisions. This question, of comparative importance or equivalence of value, is very difficult to determine. It may be considered from the point of view of speciality or isolation, or from that of richness and variety of animal forms. In isolation and speciality, determined by what they want as well as what they possess, the Australian and Neotropical regions are undoubtedly each comparable with the rest of the earth (Arctogæa). But in richness and variety of forms, they are both very much inferior, and are much more nearly comparable with the separate regions which compose it. Taking the families of mammalia as established by the best authors, and leaving out the Cetacea and the Bats, which are almost universally distributed, and about whose classification there is much uncertainty, the number of families represented in each of Mr. Sclater's regions is as follows: I. Palæarctic region has 31 families of terrestrial mammalia. II. Ethiopian " " 40 " " " III. Indian " " 31 " " " IV. Australian " " 14 " " " V. Neotropical " " 26 " " " VI. Nearctic " " 23 " " " {65}We see, then, that even the exceedingly rich and isolated Neotropical region is less rich and diversified in its forms of mammalian life than the very much smaller area of the Indian region, or the temperate Palæarctic, and very much less so than the Ethiopian region; while even the comparatively poor Nearctic region, is nearly equal to it in the number of its family types. If these were united they would possess fifty-five families, a number very disproportionate to those of the remaining two. Another consideration is, that although the absence of certain forms of life makes a region more isolated, it does not make it zoologically more important; for we have only to suppose some five or six families, now common to both, to become extinct either in the Ethiopian or the Indian regions, and they would become as strongly differentiated from all other regions as South America, while still remaining as rich in family types. In birds exactly the same phenomenon recurs, the family types being less numerous in South America than in either of the other tropical regions of the earth, but a larger proportion of them are restricted to it. It will be shown further on, that the Ethiopian and Indian, (or, as I propose to call it in this work, Oriental) regions, are sufficiently differentiated by very important groups of animals peculiar to each; and that, on strict zoological principles they are entitled to rank as regions of equal value with the Neotropical and Australian. It is perhaps less clear whether the Palæarctic should be separated from the Oriental region, with which it has undoubtedly much in common; but there are many and powerful reasons for keeping it distinct. There is an unmistakably different facies in the animal forms of the two regions; and although no families of mammalia or birds, and not many genera, are wholly confined to the Palæarctic region, a very considerable number of both have their metropolis in it, and are very richly represented. The distinction between the characteristic forms of life in tropical and cold countries is, on the whole, very strongly marked in the northern hemisphere; and to refuse to recognise this in a subdivision of the earth which is established for the very purpose of expressing such contrasts more clearly and concisely than by ordinary geographical terminology, would be both illogical and {66}inconvenient. The one question then remains, whether the Nearctic region should be kept separate, or whether it should form part of the Palæarctic or of the Neotropical regions. Professor Huxley and Mr. Blyth advocate the former course; Mr. Andrew Murray (for mammalia) and Professor Newton (for birds) think the latter would be more natural. No doubt much is to be said for both views, but both cannot be right; and it will be shown in the latter part of this chapter that the Nearctic region is, on the whole, fully as well defined as the Palæarctic, by positive characters which differentiate it from both the adjacent regions. More evidence in the same direction will be found in the Second Part of this work, in which the extinct faunas of the several regions are discussed. A confirmation of the general views here set forth, as to the distinctness and approximate equivalence of the six regions, is to be found in the fact, that if any two or more of them are combined they themselves become divisions of the next lower rank, or "sub-regions;"--and these will be very much more important, both zoologically and geographically, than the subdivisions of the remaining regions. It is admitted then that these six regions are by no means of precisely equal rank, and that some of them are far more isolated and better characterized than others; but it is maintained that, looked at from every point of view, they are more equal in rank than any others that can be formed; while in geographical equality, compactness of area, and facility of definition, they are beyond all comparison better than any others that have yet been proposed for the purpose of facilitating the study of geographical distribution. They may be arranged and grouped as follows, so as to exhibit their various relations and affinities. Regions. { NEOTROPICAL Austral zone Notogæa. Neogæa { { NEARCTIC } } } Boreal zone } { PALÆARCTIC } } { } Arctogæa. { ETHIOPIAN } } Palæogæa { } Palæotropical zone } { ORIENTAL } } { { AUSTRALIAN Austral zone Notogæa. The above table shows the regions placed in the order followed in the Fourth Part of this work, and the reasons for which are {67}explained in Chapter IX. As a matter of convenience, and for other reasons adduced in the same chapter, the detailed exposition of the geographical distribution of the animals of the several regions in Part III. commences with the Palæarctic and terminates with the Nearctic region. _Objections to the system of Circumpolar Zones._--Mr. Allen's system of "realms" founded on climatic zones (given at p. 61), having recently appeared in an ornithological work of considerable detail and research, calls for a few remarks. The author continually refers to the "_law of the distribution of life in circumpolar zones_," as if it were one generally accepted and that admits of no dispute. But this supposed "law" only applies to the smallest details of distribution--to the range and increasing or decreasing numbers of _species_ as we pass from north to south, or the reverse; while it has little bearing on the great features of zoological geography--the limitation of groups of _genera_ and _families_ to certain areas. It is analogous to the "_law of adaptation_" in the organisation of animals, by which members of various groups are suited for an aerial, an aquatic, a desert, or an arboreal life; are herbivorous, carnivorous, or insectivorous; are fitted to live underground, or in fresh waters, or on polar ice. It was once thought that these adaptive peculiarities were suitable foundations for a classification,--that whales were fishes, and bats birds; and even to this day there are naturalists who cannot recognise the essential diversity of structure in such groups as swifts and swallows, sun-birds and humming-birds, under the superficial disguise caused by adaptation to a similar mode of life. The application of Mr. Allen's principle leads to equally erroneous results, as may be well seen by considering his separation of "the southern third of Australia" to unite it with New Zealand as one of his secondary zoological divisions. If there is one country in the world whose fauna is strictly homogeneous, that country is Australia; while New Guinea on the one hand, and New Zealand on the other, are as sharply differentiated from Australia as any adjacent parts of the same primary zoological division can possibly be. Yet the "_law of circumpolar distribution_" leads to the division of {68}Australia by an arbitrary east and west line, and a union of the northern two-thirds with New Guinea, the southern third with New Zealand. Hardly less unnatural is the supposed equivalence of South Africa (the African temperate realm) to all tropical Africa and Asia, including Madagascar (the Indo-African tropical realm). South Africa has, it is true, some striking peculiarities; but they are absolutely unimportant as compared with the great and radical differences between tropical Africa and tropical Asia. On these examples we may fairly rest our rejection of Mr. Allen's scheme. We must however say a few words on the zoo-geographical nomenclature proposed in the same paper, which seems also very objectionable. The following terms are proposed: _realm_, _region_, _province_, _district_, _fauna and flora_; the first being the highest, the last the lowest and smallest sub-division. Considering that most of these terms have been used in very different senses already, and that no means of settling their equivalence in different parts of the globe has been even suggested, such a complex system must lead to endless confusion. Until the whole subject is far better known and its first principles agreed upon, the simpler and the fewer the terms employed the better; and as "region" was employed for the primary divisions by Mr. Sclater, eighteen years ago, and again by Mr. Andrew Murray, in his Geographical Distribution of Mammals; nothing but obscurity can result from each writer using some new, and doubtfully better, term. For the sub-divisions of the regions no advantage is gained by the use of a distinct term--"province"--which has been used (by Swainson) for the primary divisions, and which does not itself tell you what rank it holds; whereas the term "sub-region" speaks for itself as being unmistakably next in subordination to region, and this clearness of meaning gives it the preference over any independent term. As to minor named sub-divisions, they seem at present uncalled for; and till the greater divisions are themselves generally agreed on, it seems better to adopt no technical names for what must, for a long time to come, be indeterminate. _Does the Arctic Fauna characterize an independent {69}Region._--The proposal to consider the Arctic regions as constituting one of the primary zoological divisions of the globe, has been advocated by many naturalists. Professor Huxley seems to consider it advisable, and Mr. Allen unhesitatingly adopts it, as well as an "antarctic" region to balance it in the southern hemisphere. The reason why an "Arctic Region" finds no place in this work may therefore be here stated. No species or group of animals can properly be classed as "arctic," which does not exclusively inhabit or greatly preponderate in arctic lands. For the purpose of establishing the need of an "arctic" zoological region, we should consider chiefly such groups as are circumpolar as well as arctic; because, if they are confined to, or greatly preponderate in, either the eastern or western hemispheres, they can be at once allocated to the Nearctic or Palæarctic regions, and can therefore afford no justification for establishing a new primary division of the globe. Thus restricted, only three genera of land mammalia are truly arctic: _Gulo_, _Myodes_, and _Rangifer_. Two species of widely dispersed genera are also exclusively arctic, _Ursus maritimus_ and _Vulpes lagopus_. Exclusively arctic birds are not much more numerous. Of land birds there are only three genera (each consisting of but a single species), _Pinicola_, _Nyctea_, and _Surnia_. _Lagopus_ is circumpolar, but the genus has too wide an extension in the temperate zone to be considered arctic. Among aquatic birds we have the genus of ducks, _Somateria_; three genera of Uriidæ, _Uria_, _Catarractes_, and _Mergulus_; and the small family Alcidæ, consisting of the genera _Alca_ and _Fratercula_. Our total then is, three genera of mammalia, three of land, and six of aquatic birds, including one peculiar family. In the southern hemisphere there is only the single genus _Aptenodytes_ that can be classed as antarctic; and even that is more properly south temperate. In dealing with this arctic fauna we have two courses open to us; we must either group them with the other species and genera which are common to the two northern regions, or we {70}must form a separate primary region for them. As a matter of convenience the former plan seems the best; and it is that which is in accordance with our treatment of other intermediate tracts which contain special forms of life. The great desert zone, extending from the Atlantic shores of the Sahara across Arabia to Central Asia, is a connecting link between the Palæarctic, Ethiopian, and Oriental regions, and contains a number of "desert" forms wholly or almost wholly restricted to it; but the attempt to define it as a separate region would introduce difficulty and confusion. Neither to the "desert" nor to the "arctic" regions could any defined limits, either geographical or zoological, be placed; and the attempt to determine what species or genera should be allotted to them would prove an insoluble problem. The reason perhaps is, that both are essentially unstable, to a much greater extent than those great masses of land with more or less defined barriers, which constitute our six regions. The Arctic Zone has been, within a recent geological period, both vastly more extensive and vastly less extensive than it is at present. At a not distant epoch it extended over half of Europe and of North America. At an earlier date it appears to have vanished altogether; since a luxuriant vegetation of tall deciduous trees and broad-leaved evergreens flourished within ten degrees of the Pole! The great deserts have not improbably been equally fluctuating; hence neither the one nor the other can present that marked individuality in their forms of life, which seems to have arisen only when extensive tracts of land have retained some considerable stability both of surface and climatal conditions, during periods sufficient for the development and co-adaptation of their several assemblages of plants and animals. We must also consider that there is no geographical difficulty in dividing the Arctic Zone between the two northern regions. The only debateable lands, Greenland and Iceland, are generally admitted to belong respectively to America and Europe. Neither is there any zoological difficulty; for the land mammalia and birds are on the whole wonderfully restricted to their respective regions even in high latitudes; and the aquatic forms {71}are, for our present purpose, of much less importance. As a primary division the "Arctic region" would be out of all proportion to the other six, whether as regards its few peculiar types or the limited number of forms and species actually inhabiting it; but it comes in well as a connecting link between two regions, where the peculiar forms of both are specially modified; and is in this respect quite analogous to the great desert zone above referred to. I now proceed to characterize briefly the six regions adopted in the present work, together with the sub-regions into which they may be most conveniently and naturally divided, as shown in our general map. _Palæarctic Region._--This very extensive region comprises all temperate Europe and Asia, from Iceland to Behring's Straits and from the Azores to Japan. Its southern boundary is somewhat indefinite, but it seems advisable to comprise in it all the extra-tropical part of the Sahara and Arabia, and all Persia, Cabul, and Beloochistan to the Indus. It comes down to a little below the upper limit of forests in the Himalayas, and includes the larger northern half of China, not quite so far down the coast as Amoy. It has been said that this region differs from the Oriental by negative characters only; a host of tropical families and genera being absent, while there is little or nothing but peculiar species to characterize it absolutely. This however is not true. The Palæarctic region is well characterized by possessing 3 families of vertebrata peculiar to it, as well as 35 peculiar genera of mammalia, and 57 of birds, constituting about one-third of the total number it possesses. These are amply sufficient to characterize a region positively; but we must also consider the absence of many important groups of the Oriental, Ethiopian, and Nearctic regions; and we shall then find, that taking positive and negative characters together, and making some allowance for the necessary poverty of a temperate as compared with tropical regions, the Palæarctic is almost as strongly marked and well defined as any other. _Sub-divisions of the Palæarctic Region._--These are by no means {72}so clearly indicated as in some of the other regions, and they are adopted more for convenience than because they are very natural or strongly marked. The first, or European sub-region, comprises Central and Northern Europe as far South as the Pyrenees, the Maritime and Dinaric Alps, the Balkan mountains, the Black Sea, and the Caucasus. On the east the Caspian sea and the Ural mountains seem the most obvious limit; but it is doubtful if they form the actual boundary, which is perhaps better marked by the valley of the Irtish, where a pre-glacial sea almost certainly connected the Aral and Caspian seas with the Arctic ocean, and formed an effective barrier which must still, to some extent, influence the distribution of animals. The next, or Mediterranean sub-region, comprises South Europe, North Africa with the extra-tropical portion of the Sahara, and Egypt to about the first or second cataracts; and eastward through Asia Minor, Persia, and Cabul, to the deserts of the Indus. The third, or Siberian sub-region, consists of all north and central Asia north of Herat, as far as the eastern limits of the great desert plateau of Mongolia, and southward to about the upper limit of trees on the Himalayas. The fourth, or Manchurian sub-region, consists of Japan and North China with the lower valley of the Amoor; and it should probably be extended westward in a narrow strip along the Himalayas, embracing about 1,000 or 2,000 feet of vertical distance below the upper limit of trees, till it meets an eastern extension of the Mediterranean sub-region a little beyond Simla. These extensions are necessary to avoid passing from the Oriental region, which is essentially tropical, directly to the Siberian sub-region, which has an extreme northern character; whereas the Mediterranean and Manchurian sub-regions are more temperate in climate. It will be found that between the upper limit of most of the typical Oriental groups and the Thibetan or Siberian fauna, there is a zone in which many forms occur common to temperate China. This is especially the case among the pheasants and finches. {73}_Ethiopian Region._--The limits of this region have been indicated by the definition of the Palæarctic region. Besides Africa south of the tropic of Cancer, and its islands, it comprises the southern half of Arabia. This region has been said to be identical in the main characters of its mammalian fauna with the Oriental region, and has therefore been united with it by Mr. A. Murray. Most important differences have however been overlooked, as the following summary of the peculiarities of the Ethiopian region will, I think, show. It possesses 22 peculiar families of vertebrates; 90 peculiar genera of mammalia, being two-thirds of its whole number; and 179 peculiar genera of birds, being three-fifths of all it possesses. It is further characterized by the absence of several families and genera which range over the whole northern hemisphere, details of which will be found in the chapter treating of the region. There are, it is true, many points of resemblance, not to be wondered at between two tropical regions in the same hemisphere, and which have evidently been at one time more nearly connected, both by intervening lands and by a different condition of the lands that even now connect them. But these resemblances only render the differences more remarkable; since they show that there has been an ancient and long-continued separation of the two regions, developing a distinct fauna in each, and establishing marked specialities which the temporary intercommunication and immigration has not sufficed to remove. The entire absence of such wide-spread groups as bears and deer, from a country many parts of which are well adapted to them, and in close proximity to regions where they abound, would alone mark out the Ethiopian region as one of the primary divisions of the earth, even if it possessed a less number than it actually does of peculiar family and generic groups. _Sub-divisions of the Ethiopian Region._--The African continent south of the tropic of Cancer is more homogeneous in its prominent and superficial zoological features than most of the other regions, but there are nevertheless important and {74}deep-seated local peculiarities. Two portions can be marked off as possessing many peculiar forms; the luxuriant forest district of equatorial West Africa, and the southern extremity or Cape district. The remaining portion has no well-marked divisions, and a large proportion of its animal forms range over it from Nubia and Abyssinia, to Senegal on the one side and to the Zambesi on the other; this forms our first or East-African sub-region. The second, or West African sub-region extends along the coast from Senegal to Angola, and inland to the sources of the Shary and the Congo. The third, or South African sub-region, comprises the Cape Colony and Natal, and is roughly limited by a line from Delagoa Bay to Walvish Bay. The fourth, or Malagasy sub-region, consists of Madagascar and the adjacent islands, from Rodriguez to the Seychelles; and this differs so remarkably from the continent that it has been proposed to form a distinct primary region for its reception. Its productions are indeed highly interesting; since it possesses 3 families, and 2 sub-families of mammals peculiar to itself, while almost all its genera are peculiar. Of these a few show Oriental or Ethiopian affinities, but the remainder are quite isolated. Turning to other classes of animals, we find that the birds are almost as remarkable; but, as might be expected, a larger number of genera are common to surrounding countries. More than 30 genera are altogether peculiar, and some of these are so isolated as to require to be classed in separate families or sub-families. The African affinity is however here more strongly shown by the considerable number (13) of peculiar Ethiopian genera which in Madagascar have representative species. There can be no doubt therefore about Madagascar being more nearly related to the Ethiopian than to any other region; but its peculiarities are so great, that, were it not for its small size and the limited extent of its fauna, its claim to rank as a separate region might not seem unreasonable. It is true that it is not poorer in mammals than Australia; but that country is far more isolated, and cannot be so decidedly and {75}naturally associated with any other region as Madagascar can be with the Ethiopian. It is therefore the better and more natural course to keep it as a sub-region; the peculiarities it exhibits being of exactly the same kind as those presented by the Antilles, by New Zealand, and even by Celebes and Ceylon, but in a much greater degree. _Oriental Region._--On account of the numerous objections that have been made to naming a region from the least characteristic portion of it, and not thinking "Malayan," proposed by Mr. Blanford, a good term, (as it has a very circumscribed and definite meaning, and especially because the "Malay" archipelago is half of it in the Australian region,) I propose to use the word "Oriental" instead of "Indian," as being geographically applicable to the whole of the countries included in the region and to very few beyond it; as being euphonious, and as being free from all confusion with terms already used in zoological geography. I trust therefore that it may meet with general acceptance. This small, compact, but rich and varied region, consists of all India and China from the limits of the Palæarctic region; all the Malay peninsula and islands as far east as Java and Baly, Borneo and the Philippine Islands; and Formosa. It is positively characterized by possessing 12 peculiar families of vertebrata; by 55 genera of land mammalia, and 165 genera of land birds, altogether confined to it; these peculiar genera forming in each case about one half of the total number it possesses. _Sub-divisions of the Oriental region._--First we have the Indian sub-region, consisting of Central India from the foot of the Himalayas in the west, and south of the Ganges to the east, as far as a line drawn from Goa curving south and up to the Kistna river; this is the portion which has most affinity with Africa. The second, or Ceylonese sub-region, consists of the southern extremity of India with Ceylon; this is a mountainous forest region, and possesses several peculiar forms as well as some Malayan types not found in the first sub-region. {76}Next we have the Indo-Chinese sub-region, comprising South China and Burmah, extending westward along the Himalayan range to an altitude of about 9,000 or 10,000 feet, and southward to Tavoy or Tenasserim. The last is the Indo-Malayan sub-region, comprising the Peninsula of Malacca and the Malay Islands to Baly, Borneo, and the Philippines. On account of the absence from the first sub-region of many of the forms most characteristic of the other three, and the number of families and genera of mammalia and birds which occur in it and also in Africa, it has been thought by some naturalists that this part of India has at least an equal claim to be classed as a part of the Ethiopian region. This question will be found fully discussed in Chapter XII. devoted to the Oriental region, where it is shown that the African affinity is far less than has been represented, and that in all its essential features Central India is wholly Oriental in its fauna. Before leaving this region a few words may be said about Lemuria, a name proposed by Mr. Sclater for the site of a supposed submerged continent extending from Madagascar to Ceylon and Sumatra, in which the Lemuroid type of animals was developed. This is undoubtedly a legitimate and highly probable supposition, and it is an example of the way in which a study of the geographical distribution of animals may enable us to reconstruct the geography of a bygone age. But we must not, as Mr. Blyth proposed, make this hypothetical land one of our actual Zoological regions. It represents what was probably a primary Zoological region in some past geological epoch; but what that epoch was and what were the limits of the region in question, we are quite unable to say. If we are to suppose that it comprised the whole area now inhabited by Lemuroid animals, we must make it extend from West Africa to Burmah, South China, and Celebes; an area which it possibly did once occupy, but which cannot be formed into a modern Zoological region without violating much more important affinities. If, on the other hand, we leave out all those areas which undoubtedly belong to other regions, we reduce Lemuria to Madagascar and its adjacent {77}islands, which, for reasons already stated, it is not advisable to treat as a primary Zoological region. The theory of this ancient continent and the light it may throw on existing anomalies of distribution, will be more fully considered in the geographical part of this work. _Australian Region._--Mr. Sclater's original name seems preferable to Professor Huxley's, "Austral-Asian;" the inconvenience of which alteration is sufficiently shown by the fact that Mr. Blyth proposed to use the very same term as an appropriate substitute for the "Indian region" of Mr. Sclater. Australia is the great central mass of the region; it is by far the richest in varied and highly remarkable forms of life; and it therefore seems in every way fitted to give a name to the region of which it is the essential element. The limits of this region in the Pacific are somewhat obscure, but as so many of the Pacific Islands are extremely poor zoologically, this is not of great importance. _Sub-divisions of the Australian Region._--The first sub-region is the Austro-Malayan, including the islands from Celebes and Lombock on the west to the Solomon Islands on the east. The Australian sub-region comes next, consisting of Australia and Tasmania. The third, or Polynesian sub-region, will consist of all the tropical Pacific Islands, and is characterized by several peculiar genera of birds which are all allied to Australian types. The fourth, consists of New Zealand with Auckland, Chatham, and Norfolk Islands, and must be called the New Zealand sub-region. The extreme peculiarities of New Zealand, due no doubt to its great isolation and to its being the remains of a more extensive land, have induced several naturalists to suggest that it ought justly to form a Zoological region by itself. But the inconveniences of such a procedure have been already pointed out; and when we look at its birds as a whole (they being the only class sufficiently well represented to found any conclusion upon) we find that the majority of them belong to Australian genera, and where the genera are peculiar they are most nearly related to Australian types. The preservation in these islands {78}of a single representative of a unique order of reptiles, is, as before remarked, of the same character as the preservation of the _Proteus_ in the caverns of Carniola; and can give the locality where it happens to have survived no claim to form a primary Zoological region, unless supported by a tolerably varied and distinctly characterized fauna, such as never exists in a very restricted and insular area. _Neotropical Region._--Mr. Sclater's original name for this region is preserved, because change of nomenclature is always an evil; and neither Professor Huxley's suggested alteration "Austro-Columbia," nor Mr. Sclater's new term "Dendrogæa," appear to be improvements. The region is essentially a tropical one, and the extra-tropical portion of it is not important enough to make the name inappropriate. That proposed by Professor Huxley is not free from the same kind of criticism, since it would imply that the region was exclusively South American, whereas a considerable tract of North America belongs to it. This region includes South America, the Antilles and tropical North America; and it possesses more peculiar families of vertebrates and genera of birds and mammalia than any other region. _Subdivisions of the Neotropical Region._--The great central mass of South America, from the shores of Venezuela to Paraguay and Eastern Peru, constitutes the chief division, and may be termed the Brazilian sub-region. It is on the whole a forest country; its most remarkable forms are highly developed arboreal types; and it exhibits all the characteristics of this rich and varied continent in their highest development. The second, or Chilian sub-region, consists of the open plains, pampas, and mountains of the southern extremity of the continent; and we must include in it the west side of the Andes as far as the limits of the forest near Payta, and the whole of the high Andean plateaus as far as 4° of south latitude; which makes it coincide with the range of the Camelidæ and Chinchillidæ. The third, or Mexican sub-region, consists of Central America and Southern Mexico, but it has no distinguishing {79}characteristics except the absence of some of the more highly specialized Neotropical groups. It is, however, a convenient division as comprising the portion of the North American continent which belongs zoologically to South America. The fourth, or Antillean sub-region, consists of the West India islands (except Trinidad and Tobago, which are detached portions of the continent and must be grouped in the first sub-region); and these reproduce, in a much less marked degree, the phenomena presented by Madagascar. Terrestrial mammals are almost entirely wanting, but the larger islands possess three genera which are altogether peculiar to them. The birds are of South American forms, but comprise many peculiar genera. Terrestrial molluscs are more abundant and varied than in any part of the globe of equal extent; and if these alone were considered, the Antilles would constitute an important Zoological region. _Nearctic Region._--This region comprises all temperate North America and Greenland. The arctic lands and islands beyond the limit of trees form a transitional territory to the Palæarctic region, but even here there are some characteristic species. The southern limit between this region and the Neotropical is a little uncertain; but it may be drawn at about the Rio Grande del Norte on the east coast, and a little north of Mazatlan on the west; while on the central plateau it descends much farther south, and should perhaps include all the open highlands of Mexico and Guatemala. This would coincide with the range of several characteristic Nearctic genera. _Distinction of the Nearctic from the Palæarctic Region._--The Nearctic region possesses twelve peculiar families of vertebrates or one-tenth of its whole number. It has also twenty-four peculiar genera of mammalia and fifty-two of birds, in each case nearly one-third of all it possesses. This proportion is very nearly the same as in the Palæarctic region, while the number of peculiar families of vertebrata is very much greater. It has been already seen that both Mr. Blyth and Professor Huxley are disposed to unite this region with the Palæarctic, while Professor Newton, in his article on birds in the new edition of the {80}Encyclopædia Britannica, thinks that as regards that class it can hardly claim to be more than a sub-region of the Neotropical. These views are mutually destructive, but it will be shown in the proper place, that on independent grounds the Nearctic region can very properly be maintained. _Subdivisions of the Nearctic Region._--The sub-regions here depend on the great physical features of the country, and have been in some cases accurately defined by American naturalists. First we have the Californian sub-region, consisting of California and Oregon--a narrow tract between the Sierra Nevada and the Pacific, but characterized by a number of peculiar species and by several genera found nowhere else in the region. The second, or Rocky Mountain sub-region, consists of this great mountain range with its plateaus, and the central plains and prairies to about 100° west longitude, but including New Mexico and Texas in the South. The third and most important sub-region, which may be termed the Alleghanian, extends eastward to the Atlantic, including the Mississippi Valley, the Alleghany Mountains, and the Eastern United States. This is an old forest district, and contains most of the characteristic animal types of the region. The fourth, or Canadian sub-region, comprises all the northern part of the continent from the great lakes to the Arctic ocean; a land of pine-forests and barren wastes, characterized by Arctic types and the absence of many of the genera which distinguish the more southern portions of the region. _Observations on the series of Sub-regions._--The twenty-four sub-regions here adopted were arrived at by a careful consideration of the distribution of the more important genera, and of the materials, both zoological and geographical, available for their determination; and it was not till they were almost finally decided on, that they were found to be equal in number throughout all the regions--four in each. As this uniformity is of great advantage in tabular and diagrammatic presentations of the distribution of the several families, I decided not to disturb it unless very strong reasons should appear for adopting a greater or less number in any particular case. Such however have not {81}arisen; and it is hoped that these divisions will prove as satisfactory and useful to naturalists in general as they have been to the author. Of course, in a detailed study of any region much more minute sub-division may be required; but even in that case it is believed that the sub-regions here adopted, will be found, with slight modifications, permanently available for exhibiting general results. I give here a table showing the proportionate richness and speciality of each region as determined by its _families_ of vertebrates and _genera_ of mammalia and birds; and also a general table of the regions and sub-regions, arranged in the order that seems best to show their mutual relations. COMPARATIVE RICHNESS OF THE SIX REGIONS. +-------------+-----------------+ | | VERTEBRATA. | | REGIONS. |Families|Peculiar| | | |families| +-------------+--------+--------+ | Palæarctic | 136 | 3 | | Ethiopian | 174 | 22 | | Oriental | 164 | 12 | | Australian | 141 | 30 | | Neotropical | 168 | 44 | | Nearctic | 122 | 12 | +-------------+--------+--------+ +-------------+-----------------------+-----------------------+ | | MAMMALIA. | BIRDS. | | REGIONS. |Genera|Peculiar| Per |Genera|Peculiar| Per | | | |genera |centage| |genera |centage| +-------------+------+--------+-------+------+--------+-------+ | Palæarctic | 100 | 35 | 35 | 174 | 57 | 33 | | Ethiopian | 140 | 90 | 64 | 294 | 179 | 60 | | Oriental | 118 | 55 | 46 | 340 | 165 | 48 | | Australian | 72 | 44 | 61 | 298 | 189 | 64 | | Neotropical | 130 | 103 | 79 | 683 | 576 | 86 | | Nearctic | 74 | 24 | 32 | 169 | 52 | 31 | +-------------+------+--------+-------+------+--------+-------+ TABLE OF REGIONS AND SUB-REGIONS. +--------------+-----------------------------+--------------------------+ | Regions. | Sub-regions. | Remarks. | +--------------+-----------------------------+--------------------------+ |I. Palæarctic |1. North Europe. | | | |2. Mediterranean (or S. Eu.) |Transition to Ethiopian. | | |3. Siberia. |Transition to Nearctic. | | |4. Manchuria (or Japan) |Transition to Oriental. | | | | | |II. Ethiopian |1. East Africa. |Transition to Palæarctic. | | |2. West Africa. | | | |3. South Africa. | | | |4. Madagascar. | | | | | | |III. Oriental |1. Hindostan(or Central Ind.)|Transition to Ethiopian. | | |2. Ceylon. | | | |3. Indo-China (or Himalayas) |Transition to Palæarctic. | | |4. Indo-Malaya. |Transition to Australian. | | | | | |IV. Australian|1. Austro-Malaya. |Transition to Oriental. | | |2. Australia. | | | |3. Polynesia. | | | |4. New Zealand. |Transition to Neotropical.| | | | | |V. Neotropical|1. Chili (or S. Temp. Am.) |Transition to Australian. | | |2. Brazil. | | | |3. Mexico (or Trop. N. Am.) |Transition to Nearctic. | | |4. Antilles. | | | | | | |VI. Nearctic |1. California. | | | |2. Rocky Mountains. |Transition to Neotropical.| | |3. Alleghanies (or East U.S.)| | | |4. Canada. |Transition to Palæarctic. | +--------------+-----------------------------+--------------------------+ {83}CHAPTER V. CLASSIFICATION AS AFFECTING THE STUDY OF GEOGRAPHICAL DISTRIBUTION. A little consideration will convince us, that no inquiry into the causes and laws which determine the geographical distribution of animals or plants can lead to satisfactory results, unless we have a tolerably accurate knowledge of the affinities of the several species, genera, and families to each other; in other words, we require a natural classification to work upon. Let us, for example, take three animals--_a_, _b_, and _c_--which have a general external resemblance to each other, and are usually considered to be really allied; and let us suppose that _a_ and _b_ inhabit the same or adjacent districts, while c is found far away on the other side of the globe, with no animals at all resembling it in any of the intervening countries. We should here have a difficult problem to solve; for we should have to show that the general laws by which we account for the main features of distribution, will explain this exceptional case. But now, suppose some comparative anatomist takes these animals in hand, and finds that the resemblance of _c_ to _a_ and _b_ is only superficial, while their internal structure exhibits marked and important differences; and that _c_ really belongs to another group of animals, _d_, which inhabits the very region in which _c_ was found--and we should no longer have anything to explain. This is no imaginary case. Up to a very few years ago a curious Mexican animal, _Bassaris astuta_, was almost always classed in the civet family (Viverridæ), a group entirely {84}confined to Africa and Asia; but it has now been conclusively shown by Professor Flower that its real affinities are with the racoons (Procyonidæ), a group confined to North and South America. In another case, however, an equally careful examination shows, that an animal peculiar to the Himalayas (_Ælurus fulgens_) has its nearest ally in the _Cercoleptes_ of South America. Here, therefore, the geographical difficulty really exists, and any satisfactory theory of the causes that have led to the existing distribution of living things, must be able to account, more or less definitely, for this and other anomalies. From these cases it will be evident, that if any class or order of animals is very imperfectly known and its classification altogether artificial, it is useless to attempt to account for the anomalies its distribution may present; since those anomalies may be, to a great extent, due to false notions as to the affinities of its component species. According to the laws and causes of distribution discussed in the preceding chapters, we should find limited and defined distribution to be the rule, universal or indefinite distribution to be the exception, in every natural group corresponding to what are usually regarded as families and genera; and so much is this the case in nature, that when we find a group of this nominal rank scattered as it were at random over the earth, we have a strong presumption that it is not natural; but is, to a considerable extent, a haphazard collection of species. Of course this reasoning will only apply, in cases where there are no unusual means of dispersal, nor any exceptional causes which might determine a scattered distribution. From the considerations now adduced it becomes evident, that it is of the first importance for the success of our inquiry to secure a natural classification of animals, especially as regards the families and genera. The higher groups, such as classes and orders, are of less importance for our purpose; because they are almost always widely and often universally distributed, except those which are so small as to be evidently the nearly extinct representatives of a once more extensive series of forms. We now proceed to explain the classification to be adopted, as low down as the series of families. To these, equivalent English {85}names are given wherever they exist, in order that readers possessing no technical knowledge, may form some conception of the meaning of the term "family" in zoology. The primary divisions of the animal kingdom according to two eminent modern authorities are as follows: HUXLEY. CARUS AND GERSTAEKER. Classification of Animals Handbuch der Zoologie (1869). (1868). 1. Protozoa } } 1. Protozoa. 2. Infusoria } 3. Coelenterata 2. Coelenterata. 4. Annuloida 3. Echinodermata. { 4. Vermes. 5. Annulosa { { 5. Arthropoda. 6. Molluscoida 6. Molluscoida. 7. Mollusca 7. Mollusca. 8. Vertebrata 8. Vertebrata. For reasons already stated it is only with the fifth, seventh, and eighth of these groups that the present work proposes to deal; and even with the fifth and seventh only partially and in the most general way. The classes of the vertebrata, according to both the authors above quoted, are: 1. Mammalia. 2. Aves. 3. Reptilia. 4. Amphibia. 5. Pisces, in which order they will be taken here. The sub-classes and orders of mammalia are as follows: MAMMALIA. HUXLEY (1869), FLOWER (1870). CARUS (1868). { 1. Primates. { 1. Primates { { { 5. Prosimii. { 2. Chiroptera 2. Chiroptera. { 3. Insectivora 3. Insectivora. { { 6. Carnivora. { 4. Carnivora { { { 7. Pinnipedia. Monodelphia { 5. Cetacea } { } 12. Natantia. { 6. Sirenia } { {10. Artiodactyla. { 7. Ungulata { { {11. Perissodactyla. { 8. Proboscidea 9. Proboscidea. { 9. Hyracoidea 8. Lamnungia. { 10. Rodentia 4. Rodentia. { 11. Edentata 13. Bruta. { Didelphia 12. Marsupialia 14. Marsupialia. Ornithodelphia 13. Monotremata 15. Monotremata. {86}The above series of orders is arranged according to Professor Flower's _Osteology of Mammalia_, and they will follow in this succession throughout my work. Professor Huxley arranges the same orders in a different series. In determining the manner in which the several orders shall be subdivided into families, I have been guided in my choice of classifications mainly by the degree of attention the author appears to have paid to the group, and his known ability as a systematic zoologist; and in a less degree by considerations of convenience as regards the special purposes of geographical distribution. In many cases it is a matter of great doubt whether a certain group should form several distinct families or be united into one or two; but one method may bring out the peculiarities of distribution much better than the other, and this is, in our case, a sufficient reason for adopting it. For the Primates I follow, with some modifications, the classification of Mr. St. George Mivart given in his article "Apes" in the new edition of the _Encyclopædia Britannica_, and in his paper in the _Proceedings of the Zoological Society of London_, 1865, p. 547. It is as follows: Order--PRIMATES, divided into two Sub-orders: I. Anthropoidea. II. Lemuroidea. Sub-order--ANTHROPOIDEA. Fam. Hominidæ Man. { 1. Simiidæ Anthropoid Apes. Simii { 2. Semnopithecidæ Old-world Monkeys. { 3. Cynopithecidæ Baboons and Macaques. Cebii { 4. Cebidæ American Monkeys. { 5. Hapalidæ Marmosets. Sub-order--LEMUROIDEA. Fam. 6. Lemuridæ Lemurs. 7. Tarsiidæ Tarsiers. 8. Chiromyidæ Aye-ayes. Omitting man (for reasons stated in the preface) the three first families are considered by Professor Mivart to be sub-families of Simiidæ; but as the geographical distribution of the Old World apes is especially interesting, it is thought {87}better to treat them as families, a rank which is claimed for the anthropoid apes by many naturalists. As no good systematic work on the genera and species of bats has been yet published, I adopt the five families as generally used in this country, with the genera as given in the papers of Dr. J. E. Gray and Mr. Tomes. A monograph by Dr. Peters has long been promised, and his outline arrangement was published in 1865, but this will perhaps be materially altered when the work appears. Order--CHIROPTERA. Fam. Frugivora 9. Pteropidæ Fruit-eating Bats. {Istiophora { 10. Phyllostomidæ Leaf-nosed Bats. Insectivora { { 11. Rhinolophidæ Horse-shoe Bats. { {Gymnorhini { 12. Vespertilionidæ True Bats. { 13. Noctilionidæ Dog-headed Bats. The genera of Chiroptera are in a state of great confusion, the names used by different authors being often not at all comparable, so that the few details given of the distribution of the bats are not trustworthy. We have therefore made little use of this order in the theoretical part of the work. The osteology of the Insectivora has been very carefully worked out by Professor Mivart in the _Jounral of Anatomy and Physiology_ (Vol. ii., p. 380), and I follow his classification as given there, and in the _Proceedings of the Zoological Society_ (1871). Order--INSECTIVORA. Fam. 14. Galeopithecidæ Flying Lemurs. 15. Macroscelididæ Elephant Shrews. 16. Tupaiidæ Squirrel Shrews. 17. Erinaceidæ Hedgehogs. 18. Centetidæ Tenrecs. 19. Potamogalidæ Otter Shrew. 20. Chrysochloridæ Golden Moles. 21. Talpidæ Moles. 22. Soricidæ Shrews. The next order, Carnivora, has been studied in detail by Professor Flower; and I adopt the classification given by him in the _Proceedings of the Zoological Society_, 1869, p. 4. {88}Order--CARNIVORA. Fam. { 23. Felidæ Cats, Lion, &c. { 24. Cryptoproctidæ Cryptoprocta. { Æluroidea { 25. Viverridæ Civets. { { 26. Protelidæ Aard-wolf. { { 27. Hyænidæ Hyænas. { Fissipedia { Cynoidea 28. Canidæ Dogs, Foxes, &c. { { {29. Mustelidæ Weasels. { {30. Procyonidæ Racoons. { Arctoidea {31. Æluridæ Pandas. {32. Ursidæ Bears. {33. Otariidæ Eared Seals. Pinnipedia {34. Trichechidæ Walrus. {35. Phocidæ Seals. The Cetacea is one of those orders the classification of which is very unsettled. The animals comprising it are so huge, and there is so much difficulty in preserving them, that only a very few species are known with anything like completeness. A considerable number of genera and species have been described or indicated; but as many of these are founded on imperfect specimens of perhaps a single individual, it is not to be wondered at that those few naturalists who occupy themselves with the study of these large animals, cannot agree as to the proper mode of grouping them into natural families. They are, however, of but little importance to us, as almost all the species inhabit the ocean, and of only a few of them can it be said that anything is accurately known of their distribution. I therefore consider it best to follow Professor Carus, who makes a smaller number of families; but I give also the arrangement of Dr. Gray in his British Museum catalogue of whales and seals, as modified subsequently in the _Proceedings of Zoological Society_, 1870, p. 772. The Zeuglodontidæ, a family of extinct tertiary whales, are classed by Professors Owen and Carus between Cetacea and Sirenia, while Professor Huxley considers them to have been carnivorous and allied to the seals. {89}Order--CETACEA. Fam. (CARUS). Fam. (GRAY). Sub-order I.-- { Balænidæ 36. Balænidæ. Mystaceti. { Balænopteridæ 37. Balænopteridæ. { Catodontidæ 38. Catodontidæ. { { { Hyperoodontidæ. { Hyperoodontidæ 39. { Epiodontidæ. { { Xiphiadæ. { Sub-order II.-- { Monodontidæ 40. (Part of Delphinidæ.) Odontoceti { { { Platanistidæ. { { Iniadæ. { { Delphinidæ. { Delphinidæ 41. { Globiocephalidæ. { Orcadæ. { Belugidæ. { Pontoporiadæ. Extinct family Zeuglodontidæ. Order--SIRENIA. The order Sirenia, comprising the sea-cows, consists of a single family: Family 42. Manatidæ. The extensive order Ungulata comprises the three orders Pachydermata, Solidungula, and Ruminantia of the older naturalists. The following classification is that now generally adopted, the only difference of opinion being as to whether some of the groups should be classed as families or sub-families, a matter of little importance for our purpose: Order--UNGULATA. Fam. Perissodactyla or } 43. Equidæ Horses. Odd-toed Ungulates } 44. Tapiridæ Tapirs. 45. Rhinocerotidæ Rhinoceros. { Suina { 46. Hippopotamidæ Hippopotamus. { { 47. Suidæ Swine. { Artiodactyla or { Tylopoda 48. Camelidæ Camels. Even-toed Ungulates { { Tragulina 49. Tragulidæ Chevrotains. { { { 50. Cervidæ Deer. { Pecora { 51. Camelopardidæ Giraffes. { 52. Bovidæ { Cattle, Sheep, { Antelopes, &c. {90}The two next orders consist of but a single family each, viz.: Order Fam. PROBOSCIDEA 53. Elephantidæ Elephants. HYRACOIDEA 54. Hyracidæ Rock-rabbits. We now come to the Rodentia, a very extensive and difficult order, in which there is still much difference of opinion as to the details of classification, although the main outlines are pretty well settled. The foundations of a true classification of this order were laid by Mr. G. R. Waterhouse more than thirty years ago, and succeeding authors have done little more than follow his arrangement with unimportant modifications. Professor Lilljeborg, of Upsala, has however made a special study of this group of animals, and has given an original and detailed classification of all the genera. (_Systematisk Öfversigt af de Gnagande Däggdjuren, Glires. Upsala, 1866._) I follow this arrangement with a few slight modifications suggested by other naturalists, and which make it better adapted for the purposes of this work. Order--RODENTIA. Fam. { 55. Muridæ Rats. { 56. Spalacidæ Mole-rats. { 57. Dipodidæ Jerboas. { 58. Myoxidæ Dormice. { Murina { 59. Saccomyidæ Pouched Rats. { (Waterhouse) { 60. Castoridæ Beavers. { { 61. Sciuridæ Squirrels. Simplicidentati { { 62. Haploodontidæ Sewellels. { { { 63. Chinchillidæ Chinchillas. { { 64. Octodontidæ Octodons. { Hystricina { 65. Echimyidæ Spiny Rats. (Waterhouse) { 66. Cercolabidæ Tree Porcupines { 67. Hystricidæ Porcupines. { 68. Caviidæ Cavies. Duplicidentati { Leporina { 69. Lagomyidæ Pikas. { (Waterhouse) { 70. Leporidæ Hares. The Edentata have been classified by Mr. Turner, in the _Proceedings of the Zoological Society_ (1851, p. 205), by Dr. Gray in the British Museum Catalogue, and by Professor Carus in his _Handbuch_. The former takes a middle course between {91}the numerous families of Dr. Gray, seven in number, and the two families to which Professor Carus restricts the existing species. I therefore follow Mr. Turner. Order--EDENTATA. Fam. Bradypoda 71. Bradypodidæ Sloths. { 72. Manididæ Scaly Ant-eaters. { 73. Dasypodidæ Armadillos. Entomophaga { 74. Orycteropodidæ Ant-bears. { 75. Myrmecophagidæ Ant-eaters. The Marsupials have been well classified and described by Mr. Waterhouse in the first volume of his _Natural History of Mammalia_, and his arrangement is here followed. The suborders adopted by Professor Carus are also given. Order--MARSUPIALIA. Fam. { 76. Didelphidæ Opossums. { 77. Dasyuridæ Native Cats. Rapacia (Wagner) { 78. Myrmecobiidæ Native Ant-eater. { 79. Peramelidæ Bandicoots. Poephaga (Owen) 80. Macropodidæ Kangaroos. Carpophaga (Owen) 81. Phalangistidæ Phalangers. Rhizophaga (Owen) 82. Phascolomyidæ Wombats. Order--MONOTREMATA. The last order, the Monotremata, consist of two families, which Professor Carus combines into one, but which it seems more natural to keep separate. Fam. 83. Ornithorhynchidæ Duckbill. 84. Echidnidæ Echidna. {92}BIRDS. Birds are perhaps the most difficult to classify of all the divisions of the vertebrata. The species and genera are exceedingly numerous, and there is such a great uniformity in general structure and even in the details of external form, that it is exceedingly difficult to find characters by which orders and families can be characterised. For a long time the system of Vigors and Swainson was followed; but this wholly ignored anatomical characters and in many cases plainly violated well-marked affinities. Characters derived from the form of the sternum, the scutellation of the tarsi, and the arrangement of the feathers, have all assisted in determining natural groups. More recently Professor Huxley has applied the variations of the bony palate to the general arrangement of birds; and still more recently Professor Garrod has studied certain leg-muscles for the same purpose. The condition of the young as regards plumage, and even the form, texture, and coloration of the egg, have also been applied to solve doubtful cases of affinity; yet the problem is not settled, and it will probably remain for another generation of ornithologists to determine with any approach to accuracy what are the most natural divisions of the class into orders and families. In a work like the present it is evidently not advisable to adopt all the recent classifications; since experience has shown that no arrangement in which one set of characters is mainly relied on, long holds its ground. Such modifications of the old system as seem to be well established will be adopted; but the older groups will be adhered to in cases where the most recent classifications are open to doubt, or seem inconvenient as separating families, which, owing to their similarity in general structure, form and habits are best kept together for the purposes of geographical distribution. The old plan of putting the birds of prey at the head of the class, is now almost wholly given up; both because they are not {93}the most highly organised, but only one of the most specialised forms of birds, and because their affinities are not with the Passeres, but rather with the cormorants and some other of the aquatic groups. The Passeres therefore are placed first; and the series of families is begun by the thrushes, which are certainly the most typical and generally well-organised form of birds. Instead of the Scansores and Fissirostres of the older authors, the order Picariæ, which includes them both, is adopted, but with some reluctance; as the former are, generally speaking, well marked and strongly contrasted groups, although certain families have been shown to be intermediate. In the Picariæ are included the goat-suckers, swifts, and humming-birds, sometimes separated as a distinct order, Macrochires. The parrots and the pigeons form each a separate order. The old groups of Grallæ and Anseres are preserved, as more convenient than breaking them up into widely separated parts; for though the latter plan may in some cases more strictly represent their affinities, its details are not yet established, nor is it much used by ornithologists. In accordance with these views the following is the series of orders and families of birds adopted in this work: Class--AVES. Orders. 1. Passeres { Including the great mass of the smaller birds--Crows, { Finches, Flycatchers, Creepers, Honeysuckers, &c., &c. 2. Picariæ { Including Woodpeckers, Cuckoos, Toucans, Kingfishers, { Swifts, &c., &c. 3. Psittaci Parrots only. 4. Columbæ Pigeons and the Dodo. 5. Gallinæ Grouse, Pheasants, Curassows, Mound-builders, &c. 6. Opisthocomi The Hoazin only. 7. Accipitres Eagles, Owls, and Vultures. 8. Grallæ Herons, Plovers, Rails, &c. 9. Anseres Gulls, Ducks, Divers, &c. 10. Struthiones Ostrich, Cassowary, Apteryx, &c. The Passeres consist of fifty families, which may be arranged and grouped in series as follows. It must however be remembered that the first family in each series is not always that which is most allied to the last family of the preceding series. All extensive natural groups consist of divergent or branching alliances, which renders it impossible to arrange the whole in one continuous series. {94}A.--TYPICAL OR TURDOID PASSERES. 1. Turdidæ Thrushes. 2. Sylviidæ Warblers. 3. Timaliidæ Babblers. 4. Panuridæ Reedlings. 5. Cinclidæ Dippers. 6. Troglodytidæ Wrens. 7. Chamæidæ 8. Certhiidæ Creepers. 9. Sittidæ Nuthatches. 10. Paridæ Tits. 11. Liotrichidæ Hill-tits. 12. Phyllornithidæ Green Bulbuls. 13. Pycnonotidæ Bulbuls. 14. Oriolidæ Orioles. 15. Campephagidæ Caterpillar-shrikes. 16. Dicruridæ Drougos. 17. Muscicapidæ Flycatchers. 18. Pachycephalidæ Thick-heads. 19. Laniidæ Shrikes. 20. Corvidæ Crows. 21. Paradiseidæ Paradise-birds. 22. Meliphagidæ Honey-suckers. 23. Nectarineidæ Sun-birds. B.--TANAGROID PASSERES. 24. Dicæidæ Flower-peckers. 25. Drepanididæ 26. Cærebidæ Sugar-birds. 27. Mniotiltidæ Wood-warblers. 28. Vireonidæ Greenlets. 29. Ampelidæ Waxwings. 30. Hirundinidæ Swallows. 31. Icteridæ Hangnests. 32. Tanagridæ Tanagers. 33. Fringillidæ Finches. C.--STURNOID PASSERES. 34. Ploceidæ Weaver-birds. 35. Sturnidæ Starlings. 36. Artamidæ Swallow-shrikes. 37. Alaudidæ Larks. 38. Motacillidæ Wagtails. D.--FORMICAROID PASSERES. 39. Tyrannidæ Tyrants. 40. Pipridæ Manakins. 41. Cotingidæ Chatterers. 42. Phytotomidæ Plant-cutters. 43. Eurylæmidæ Broad-bills. 44. Dendrocolaptidæ American Creepers. 45. Formicariidæ Ant-thrushes. 46. Pteroptochidæ {95} 47. Pittidæ Pittas. 48. Paictidæ E.--ANOMALOUS PASSERES. 49. Menuridæ Lyre-birds. 50. Atrichidæ Scrub-birds. The preceding arrangement is a modification of that proposed by myself in the _Ibis_ (1874, p. 406). The principal alterations are adding the families Panuridæ and Sittidæ in series A, commencing series B with Dicæidæ; bringing Vireonidæ next to the allied American family Mniotiltidæ; and placing Motacillidæ in series C next to Alaudidæ. At the suggestion of Professor Newton I place Menuridæ and Atrichidæ apart from the other Passeres, as they both possess striking peculiarities of anatomical structure. The heterogeneous families constituting the order Picariæ may be conveniently arranged as follows: { 51. Picidæ Woodpeckers. { 52. Yungidæ Wrynecks. { 53. Indicatoridæ Honey-guides. Sub-order-- { 54. Megalæmidæ Barbets. Scansores. { 55. Rhamphastidæ Toucans. { 56. Musophagidæ Plantain-eaters. { 57. Coliidæ Colies. { 58. Cuculidæ Cuckoos. Intermediate 59. Leptosomidæ The Leptosoma. { 60. Bucconidæ Puff-birds. { 61. Galbulidæ Jacamars. { 62. Coraciidæ Rollers. { 63. Meropidæ Bee-eaters. { 64. Todidæ Todies. { 65. Momotidæ Motmots. { 66. Trogonidæ Trogons. Sub-order-- { 67. Alcedinidæ Kingfishers. Fissirostres. { 68. Bucerotidæ Hornbills. { 69. Upupidæ Hoopoes. { 70. Irrisoridæ Promerops. { 71. Podargidæ Frog-mouths. { 72. Steatornithidæ The Guacharo. { 73. Caprimulgidæ Goatsuckers. { 74. Cypselidæ Swifts. { 75. Trochilidæ Humming-birds. {96}The Psittaci or parrot tribe are still in a very unsettled state of classification; that recently proposed by Professor Garrod differing widely from the arrangement adopted in Dr. Finsch's monograph of the order. Taking advantage of the researches of these and other authors, the following families are adopted as the most convenient in the present state of our knowledge: 76. Cacatuidæ The Cockatoos. 77. Platycercidæ The Broad-tailed Paroquets of Australia. 78. Palæornithidæ The Oriental Parrots and Paroquets. 79. Trichoglossidæ The Brush-tongued Paroquets and Lories. 80. Conuridæ The Macaws and their allies. 81. Psittacidæ The African and South American Parrots. 82. Nestoridæ The Nestors of New Zealand. 83. Stringopidæ The Owl-parrots of New Zealand. The Columbæ, or pigeons, are also in a very unsatisfactory state as regards a natural classification. The families, sub-families, and genera proposed by various authors are very numerous, and often quite irreconcilable. I therefore adopt only two families; and generally follow Mr. G. R. Gray's hand-list for the genera, except where trustworthy authorities exist for a different arrangement. The families are: 84. Columbidæ Pigeons and Doves. 85. Dididæ The extinct Dodo and allies. The Gallinæ, or game-birds, may be divided into seven families: Fam. Sub-fam. 86. Pteroclidæ Sand-grouse. 87. Tetraonidæ Partridges and Grouse. { Pavoninæ Peafowl. { Lophophorinæ Tragopans, &c. { Phasianinæ Pheasants. 88. Phasianidæ { Euplocaminæ Fire-backed Pheasants, &c. { Gallinæ Jungle-fowl. { Meleagrinæ Turkeys. { Numidinæ Guinea-fowl. 89. Turnicidæ Hemipodes. 90. Megapodiidæ Mound-makers. { Cracinæ Curassows. 91. Cracidæ { Penelopinæ Guans. { Oreophasinæ Mountain-pheasant. 92. Tinamidæ Tinamous. {97}The Opisthocomi consist of one family containing a single species, the "Hoatzin" of Guiana. Family 93. Opisthocomidæ. The Accipitres, or birds of prey, which were long considered to be the highest and most perfect order of birds, are now properly placed lower down in the series, their affinities being more with the aquatic than with the perching birds. The following is the arrangement adopted by Mr. Sharpe in his recently published British Museum catalogue of diurnal birds of prey:-- Sub-orders. Fam. Sub-families. { Vulturinæ Vultures. { 94. Vulturidæ { Sarcorhamphinæ Turkey-buzzards. { Falcones { 95. Serpentariidæ { { { Polyborniæ Caracaras. { { Accipitrinæ Hawks. { 96. Falconidæ { Buteoninæ Buzzards. { Aquilinæ Eagles. { Falconinæ Falcons. Pandiones 97. Pandionidæ Fishing-eagles. Striges 98. Strigidæ Owls. The Grallæ or Grallatores are in a very unsettled state. The following series of families is in accordance with the views of some of the best modern ornithologists: 99. Rallidæ Rails, &c. 100. Scolopacidæ Sandpipers and Snipes 101. Chionididæ Sheath-bills. 102. Thinocoridæ Quail-snipes. 103. Parridæ Jacanas. 104. Glareolidæ Pratincoles. 105. Charadriidæ Plovers. 106. Otididæ Bustards. 107. Gruidæ Cranes. 108. Cariamidæ Cariamas. 109. Aramidæ Guaraunas. 110. Psophiidæ Trumpeters. 111. Eurypygidæ Sun-bitterns. 112. Rhinochoetidæ Kagus. 113. Ardeidæ Herons. 114. Plataleidæ Spoonbills and Ibis. 115. Ciconiidæ Storks. 116. Palamedeidæ Screamers. 117. Phænicopteridæ Flamingoes. {98}The Anseres or Natatores are almost equally unsettled. The flamingoes are usually placed in this order, but their habits best assort with those of the waders. Fam. 118. Anatidæ Duck and Geese. 119. Laridæ Gulls. 120. Procellariidæ Petrels. 121. Pelecanidæ Pelicans. 122. Spheniscidæ Penguins. 123. Colymbidæ Divers. 124. Podicipidæ Grebes. 125. Alcidæ Auks. The last order of birds is the Struthiones or Ratitæ, considered by many naturalists to form a distinct sub-class. It consists of comparatively few species, either living or recently extinct. Fam. { 126. Struthionidæ Ostriches. Living { 127. Casuariidæ Cassowaries. { 128. Apterygidæ Apteryx. { 129. Dinornithidæ Dinornis. Extinct { 130. Palapterygidæ Palapteryx. { 131. Æpyornithidæ Æpyornis. REPTILES. In reptiles I follow the classification of Dr. Günther as given in the _Philosophical Transactions_, vol. clvii., p. 625. He divides the class into five orders as follows:-- Sub-classes. Orders. { 1. Ophidia Serpents. I. Squamata { 2. Lacertilia Lizards. { 3. Rhyncocephalina The Hatteria. II. Loricata 4. Crocodilia Crocodiles. III. Cataphracta 5. Chelonia Tortoises. In the arrangement of the families comprised in each of these orders I also follow the arrangement of Dr. Günther and Dr. J. E. Gray, as given in the British Museum Catalogue, or as modified by the former gentleman who has kindly given me much personal information. {99}The Ophidia, or Snakes, form the first order and are classified as follows:-- Fam. { 1. Typhlopidæ } { 2. Tortricidæ } { 3. Xenopeltidæ } Burrowing Snakes. { 4. Uropeltidæ } { 5. Calamaridæ Dwarf ground-snakes. { 6. Oligodontidæ. { 7. Colubridæ Colubrine Snakes. { 8. Homalopsidæ Fresh-water Snakes. { 9. Psammophidæ Desert-snakes. Innocuous Snakes { 10. Rachiodontidæ. { 11. Dendrophidæ Tree-snakes. { 12. Dryiophidæ Whip-snakes. { 13. Dipsasidæ Nocturnal tree-snakes. { 14. Scytalidæ { 15. Lycodontidæ Fanged ground-snakes. { 16. Amblycephalidæ Blunt-heads. { 17. Pythonidæ Pythons. { 18. Erycidæ Sand-snakes. { 19. Acrochordidæ Wart-snakes. { 20. Elapidæ Cobras, &c. Venomous Colubrine { 21. Dendraspididæ. Snakes { 22. Atractaspididæ. { 23. Hydrophidæ Sea-snakes. { 24. Crotalidæ Pit-vipers. Viperine Snakes { 25. Viperidæ True vipers. The second order, Lacertilia, are arranged as follows:-- Fam. 26. Trogonophidæ } 27. Chirotidæ } 28. Amphisbænidæ } Amphisbænians. 29. Lepidosternidæ } 30. Varanidæ Water Lizards. 31. Helodermidæ. 32. Teidæ Teguexins. 33. Lacertidæ } Land Lizards. 34. Zonuridæ } 35. Chalcidæ. 36. Anadiadæ. 37. Chirocolidæ. 38. Iphisadæ. 39. Cercosauridæ. 40. Chamæsauridæ. 41. Gymnopthalmidæ Gape-eyed Scinks. 42. Pygopodidæ Two-legged Lizards. 43. Aprasiadæ. 44. Lialidæ. {100} 45. Scincidæ Scinks. 46. Ophiomoridæ Snake-lizards. 47. Sepidæ Sand-lizards. 48. Acontiadæ. 49. Geckotidæ Geckoes. 50. Iguanidæ Iguanas. 51. Agamidæ Fringed Lizards. 52. Chameleonidæ Chameleons. The third order, Rhyncocephalina consists of a single family:-- 53. Rhyncocephalidæ The Hatteria of New Zealand. The fourth order, Crocodilia or Loricata, consists of three families:-- 54. Gavialidæ Gavials. 55. Crocodilidæ Crocodiles. 56. Alligatoridæ Alligators. The fifth order, Chelonia, consists of four families:-- 57. Testudinidæ Land and fresh-water Tortoises. 58. Chelydidæ Fresh-water Turtles. 59. Trionychidæ Soft Turtles. 60. Cheloniidæ Sea Turtles. AMPHIBIA. In the Amphibia I follow the classification of Professor Mivart, as given for a large part of the order in the _Proceedings of the Zoological Society_ for 1869. For the remainder I follow Dr. Strauch, Dr. Günther, and a MSS. arrangement kindly furnished me by Professor Mivart. The class is first divided into three groups or orders, and then into families as follows:-- {101}Order I.--PSEUDOPHIDIA. Fam. 1. Cæciliadæ Cæcilia. Order II.--BATRACHIA URODELA. 2. Sirenidæ Siren. 3. Proteidæ Proteus. 4. Amphiumidæ Amphiuma. 5. Menopomidæ Giant Salamanders. 6. Salamandridæ Salamanders and Newts. Order III.--BATRACHIA ANOURA. 7. Rhinophrynidæ } 8. Phryniscidæ } 9. Hylaplesidæ } Toads. 10. Bufonidæ } 11. Xenorhinidæ } 12. Engystomidæ } 13. Bombinatoridæ } 14. Plectromantidæ } Frogs. 15. Alytidæ } 16. Pelodryadæ } 17. Hylidæ } Tree Frogs. 18. Polypedatidæ } 19. Ranidæ } Frogs. 20. Discoglossidæ } 21. Pipidæ } Tongueless 22. Dactylethridæ } Toads. FISHES. These are arranged according to the classification of Dr. Günther, whose great work "The British Museum Catalogue of Fishes," has furnished almost all the material for our account of the distribution of the class. In that work all existing fishes are arranged in six sub-classes and thirteen orders. A study of the extraordinary _Ceratodus_ from Australia has induced Dr. Günther to unite three of his sub-classes; but as his catalogue will long remain a handbook for every student of fishes, it seems better to follow the arrangement there given, indicating his later views by bracketing together the groups he now thinks should be united. -----------------------------------------+---------+--------------- {102} Sub-class. Order. |Families.| Remarks. -----------------------------------------+---------+------------------ { 1. Acanthopterygii | 47 | Gasterosteidæ to { | | Notacanthi. { 2. Do. Pharyncognathi | 5 | Pomacentridæ to { | | Chromidæ. Ganoidei { 3. Acanthini | 6 | Gadopsidæ to ======== { | | Pleuronectidæ. {Teleostei { 4. Physostomi | 29 | Siluridæ to { { | | Pegasidæ. { { 5. Lophobranchii | 2 | Solenostomidæ and { { | | Syngnathidæ. { { 6. Plectognathi | 2 | Sclerodermi and { { | | Gymnodontes. { | | {Dipnoi 7. Sirenoidei | 1 | Sirenoidei. { | | { { 8. Holostei | 3 | Amiidæ to { { | | Lepidosteidæ. {Ganoidei { 9. Chondrostei | 2 | Accipenseridæ and { | | Polydontidæ. | | Chondropterygii { 10. Holocephala | 1 | Chimæridæ. { 11. Plagiostomata | 15 | Carchariidæ to | | Myliobatidæ. | | Cyclostomata 12. Marsipobranchii | 2 | Petromyzontidæ and | | Myxinidæ. | | Leptocardii 13. Cirrhostomi | 1 | Cirrhostomi. +---------+ Total 116 families. ----------------------------------------------------------------------- INSECTS. The families and genera of insects are so immensely numerous, probably exceeding fifty-fold those of all other land animals, that for this cause alone it would be impossible to enter fully into their distribution. It is also quite unnecessary, because many of the groups are so liable to be transported by accidental causes, that they afford no useful information for our subject; while others are so obscure and uninteresting that they have been very partially collected and studied, and are for this reason equally ineligible. I have therefore selected a few of the largest and most conspicuous families, which have been so assiduously collected in every part of the globe, and so carefully studied at home, as to afford valuable materials for comparison with the vertebrate groups, when we have made due allowance for the dependence of many insects on peculiar forms of vegetation, and the facility with which many of them are transported either in the egg, larva, or perfect state, by winds, currents, and other less known means. I confine myself then, almost exclusively, to the sixteen families of Diurnal Lepidoptera or butterflies, and to six of the most extensive, conspicuous, and popular families of Coleoptera. {103}The number of species of Butterflies is about the same as that of Birds, while the six families of Coleoptera selected, comprise more than twenty thousand species, far exceeding the number of all other vertebrates. These families have all been recently catalogued, so that we have very complete information as to their arrangement and distribution. LEPIDOPTERA DIURNA, OR BUTTERFLIES. Fam. 1. Danaidæ. 2. Satyridæ. 3. Elymniidæ. 4. Morphidæ. 5. Brassolidæ. 6. Acræidæ. 7. Heliconidæ. 8. Nymphalidæ. 9. Libythæidæ. 10. Nemeobiidæ. 11. Eurygonidæ. 12. Erycinidæ. 13. Lycænidæ. 14. Pieridæ. 15. Papilionidæ. 16. Hesperidæ. COLEOPTERA, OR BEETLES. Fam. 1. Cicindelidæ Tiger-beetles. 2. Carabidæ Ground-beetles. 3. Lucanidæ Stag-beetles. 4. Cetoniidæ Rose-chafers. 5. Buprestidæ Metallic Beetles. 6. Longicornia Long-horned Beetles. The above families comprise the extensive series of ground beetles (Carabidæ) containing about 9,000 species, and the Longicorns, which are nearly as numerous and surpass them in variety of form and colour as well as in beauty. The Cetoniidæ and Buprestidæ are among the largest and most brilliant of beetles; the Lucanidæ are pre-eminent for remarkable form, and the Cicindelidæ for elegance; and all the families are especial favourites with entomologists, so that the whole earth has been ransacked to procure fresh species. Results deduced from a study of these will, therefore, fairly represent the phenomena of distribution of Coleoptera, and, as they are very varied in their habits, perhaps of insects in general. {104}MOLLUSCA. The Mollusca are usually divided into five classes as follows:-- Classes. I. Cephalopoda Cuttle-fish. II. Gasteropoda Snails and aquatic Univalves. III. Pteropoda Oceanic Snails. IV. Brachiopoda Symmetrical Bivalves. V. Conchifera Unsymmetrical Bivalves. The Gasteropoda and Conchifera alone contain land and freshwater forms, and to these we shall chiefly confine our illustrations of the geographical distribution of the Mollusca. The classification followed is that of Dr. Pfeiffer for the Operculata and Dr. Von Martens for the Helicidæ. The families chiefly referred to are:-- Class II.--GASTEROPODA. Order 2.--Pulmonifera. Fam. { 1. Helicidæ. { 2. Limacidæ. { 3. Oncidiadæ. In-operculata { 4. Limnæidæ. { 5. Auriculidæ. { 6. Aciculidæ. { 7. Diplommatinidæ. Operculata { 8. Cyclostomidæ. { 9. Helicinidæ. PART II. _ON THE DISTRIBUTION OF EXTINCT ANIMALS._ {107}CHAPTER VI. THE EXTINCT MAMMALIA OF THE OLD WORLD. Although it may seem somewhat out of place to begin the systematic treatment of our subject with extinct rather than with living animals, it is necessary to do so in order that we may see the meaning and trace the causes of the existing distribution of animal forms. It is true, that the animals found fossil in a country are very generally allied to those which still inhabit it; but this is by no means universally the case. If it were, the attempt to elucidate our subject by Palæontology would be hopeless, since the past would show us the same puzzling diversities of faunas and floras that now exist. We find however very numerous exceptions to this rule, and it is these exceptions which tell us of the past migrations of whole groups of animals. We are thus enabled to determine what portion of the existing races of animals in a country are descendants of its ancient fauna, and which are comparatively modern immigrants; and combining these movements of the forms of life with known or probable changes in the distribution of land and sea, we shall sometimes be able to trace approximately the long series of changes which have resulted in the actual state of things. To gain this knowledge is our object in studying the "Geographical Distribution of Animals," and our plan of study must be determined, mainly, by the facilities it affords us for attaining this object. In discussing the countless details of distribution we shall meet with in our survey of the zoological regions, we shall often find it useful to refer to the evidence we possess of the range of the group in question in {108}past times; and when we attempt to generalise the phenomena on a large scale, with the details fresh in our memory, we shall find a reference to the extinct faunas of various epochs to be absolutely necessary. The degree of our knowledge of the Palæontology of various parts of the world is so unequal, that it will not be advisable to treat the subject under each of our six regions. Yet some subdivision must be made, and it seems best to consider separately the extinct animals of the Old and of the New Worlds. Those of Europe and Asia are intimately connected, and throw light on the past changes which have led to the establishment of the three great continental Old World regions, with their various subdivisions. The wonderful extinct fauna recently discovered in North America, with what was previously known from South temperate America, not only elucidates the past history of the whole continent, but also gives indications of the mutual relations of the eastern and western hemispheres. The materials to be dealt with are enormous; and it will be necessary to confine ourselves to a general summary, with fuller details on those points which directly bear upon our special subject. The objects of most interest to the pure zoologist and to the geologist--those strange forms which are farthest removed from any now living--are of least interest to us, since we aim at tracing the local origin or birthplace of existing genera and families; and for this purpose animals whose affinities with living forms are altogether doubtful, are of no value whatever. The great mass of the vertebrate fossils of the tertiary period consist of mammalia, and this is precisely the class which is of most value in the determination of zoological regions. The animals of the secondary period, though of the highest interest to the zoologist are of little importance to us; both because of their very uncertain affinities for any existing groups, and also because we can form no adequate notion of the distribution of land and sea in those remote epochs. Our great object is to trace back, step by step, the varying distribution of the chief forms of life; and to deduce, wherever possible, the physical changes which must have accompanied or caused such changes. {109}The natural division of our subject therefore is into geological periods. We first go back to the Post-Pliocene period, which includes that of the caves and gravels of Europe containing flint implements, and extends back to the deposit of the glacial drift in the concluding phase of the glacial epoch. Next we have the Pliocene period, divided into its later portion (the Newer Pliocene) which includes the Glacial epoch of the northern hemisphere; and its earlier portion (the Older Pliocene), represented by the red and coralline crag of England, and deposits of similar age in the continent. During this earlier epoch the climate was not very dissimilar from that which now prevails; but we next get evidence of a still earlier period, the Miocene, when a warmer climate prevailed in Europe, and the whole fauna and flora were very different. This is perhaps the most interesting portion of the tertiary deposits, and furnishes us with the most valuable materials for our present study. Further back still we have the Eocene period, with apparently an almost tropical climate in Europe; and here we find a clue to some of the most puzzling facts in the distribution of living animals. Our knowledge of this epoch is however very imperfect; and we wait for discoveries that will elucidate some of the mystery that still hangs over the origin and migrations of many important families. Beyond this there is a great chasm in the geological record as regards land animals; and we have to go so far back into the past, that when we again meet with mammalia, birds, and land-reptiles, they appear under such archaic forms that they cease to have any local or geographical significance, and we can only refer them to wide-spread classes and orders. For the purpose of elucidating geographical distribution, therefore, it is, in the present state of our knowledge, unnecessary to go back beyond the tertiary period of geology. The remains of Mammalia being so much more numerous and important than those of other classes, we shall at first confine ourselves almost exclusively to these. What is known of the birds, reptiles, and fishes of the tertiary epoch will be best indicated by a brief connected sketch of their fossils in all parts of the globe, which we shall give in a subsequent chapter. {110}_Historic Period._--In tracing back the history of the organic world we find, even within the limits of the historical period, that some animals have become extinct, while the distribution of others has been materially changed. The _Rytina_ of the North Pacific, the dodo of Mauritius, and the great auk of the North Atlantic coasts, have been exterminated almost in our own times. The kitchen-middens of Denmark contain remains of the capercailzie, the _Bos primigenius_, and the beaver. The first still abounds farther north, the second is extinct, and the third is becoming so in Europe. The great Irish elk, a huge-antlered deer, probably existed almost down to historic times. _Pleistocene or Post-Pliocene Period._--We first meet with proofs of important changes in the character of the European fauna, in studying the remains found in the caverns of England and France, which have recently been so well explored. These cave-remains are probably all subsequent to the Glacial epoch, and they all come within the period of man's occupation of the country. Yet we find clear proofs of two distinct kinds of change in the forms of animal life. First we have a change clearly traceable to a difference of climate. We find such arctic forms as the rein-deer, the musk-sheep, the glutton, and the lemming, with the mammoth and the woolly rhinoceros of the Siberian ice-cliffs, inhabiting this country and even the south of France. This is held to be good proof that a sub-arctic climate prevailed over all Central Europe; and this climate, together with the continental condition of Britain, will sufficiently explain such a southward range of what are now arctic forms. But together with this change we have another that seems at first sight to be in an exactly opposite direction. We meet with numerous animals which now only inhabit Africa, or South Europe, or the warmer parts of Asia. Such are, large felines--some closely related to the lion (_Felis spelæa_), others of altogether extinct type (_Machairodus_) and forming the extreme development of the feline race;--hyænas; horses of two or more species; and a hippopotamus. If we go a little further back, to the remains furnished by the gravels and brick-earths, we still find the same association of forms. The reindeer, the glutton, {111}the musk-sheep, and the woolly rhinoceros, are associated with several other species of rhinoceros and elephant; with numerous civets, now abundant only in warm countries; and with antelopes of several species. We also meet here with a great extension of range of forms now limited to small areas. The Saiga antelope of Eastern Europe occurs in France, where wild sheep and goats and the chamois were then found, together with several species of deer, of bear, and of hyæna. A few extinct genera even come down to this late period, such as the great sabre-toothed tiger, _Machairodus_; _Galeotherium_, a form of Viverridæ; _Palæospalax_, allied to the mole; and _Trogontherium_, a gigantic form of beaver, We find then, that even at so early a stage of our inquiries we meet with a problem in distribution by no means easy to solve. How are we to explain the banishment from Europe in so short a space of time (geologically speaking) of so many forms of life now characteristic of warmer countries, and this too during a period when the climate of Central Europe was itself becoming warmer? Such a change must almost certainly have been due to changes of physical geography, which we shall be better able to understand when we have examined the preceding Pliocene period. We may here notice, however, that so far as we yet know, this great recent change in the character of the fauna is confined to the western part of the Palæarctic region. In caves in the Altai Mountains examined by Prof. Brandt, a great collection of fossil bones was discovered. These comprised the Siberian rhinoceros and mammoth, and the cave hyæna; but all the others, more than thirty distinct species, are now living in or near the same regions. We may perhaps impute this difference to the fact that the migration of Southern types into this part of Siberia was prevented by the great mountain and desert barrier of the Central Asiatic plateau; whereas in Europe there was at this time a land connection with Africa. Post-pliocene deposits and caverns in Algeria have yielded remains resembling the more southern European types of the Post-pliocene period, but without any admixture of Arctic forms; showing, as we might expect, that the glacial cold did not {112}extend so far south. We have here remains of _Equus_, _Bos_, _Antilope_, _Hippopotamus_, _Elephas_, _Rhinoceros_, _Ursus_, _Canis_, and _Hyæna_, together with _Phacochoerus_, an African type of swine which has not occurred in the European deposits. It is perhaps to the earlier portion of this period that the _Merycotherium_ of the Siberian drift belongs. This was an animal related to the living camel, thus supporting the view that the _Camelidæ_ are essentially denizens of the extra-tropical zone. PLIOCENE PERIOD. _Primates._--We here first meet with evidence of the existence of monkeys in Central Europe. Species of _Macacus_ have left remains not only in the Newer Pliocene of the Val d'Arno in Italy, but in beds of the same age at Grays in Essex; while _Semnopithecus_ and _Cercopithecus_, genera now confined to the Oriental and Ethiopian regions respectively, have been found in the Pliocene deposits of the South of France and Italy. _Carnivora._--Most of the genera which occurred in the Post-Pliocene are found here also, and many of the same species. Few new forms appear, except _Hyænarctos_, a large bear with characters approaching the hyænas, and _Pristiphoca_, a new form of seal, both from the Older Pliocene of France; and _Galecynus_, a fox-like animal intermediate between _Canis_ and _Viverra_, from the Pliocene of Oeninghen in Switzerland. _Cetacea._--Species of _Balæna_, _Physeter_, and _Delphinus_ occur in the Older Pliocene of England and France, and with these the remains of many extinct forms, _Balænodon_ and _Hoplocetus_ (Balænidæ); _Belemnoziphius_ and _Choneziphius_ (Hyperoodontidæ), and _Halitherium_, an extinct form of the next order--Sirenia, now confined to the tropics, although the recently extinct _Rytina_ of the N. W. Pacific shows that it is also adapted for temperate climates. _Ungulata._--The Pliocene deposits are not very rich in this order. The horses (_Equidæ_) are represented by the genus _Equus_; and here we first meet with _Hipparion_, in which small lateral toes appear. Both genera occur in British deposits of this age. {113}A more interesting fact for us is the occurrence of the genus _Tapirus_ in the Newer Pliocene of France and in the older beds of both France and England, since this genus is now isolated in the remotest parts of the eastern and western tropics. The genera _Rhinoceros_, _Hippopotamus_, and _Sus_, occur here as in the preceding epoch. We next come to the deer genus (_Cervus_), which appears to have been at its maximum in this period, no less than eight species occurring in the Norwich Crag, and Forest-beds. Among the Bovidæ, the antelopes, ox, and bison, are the only forms represented here, as in the Post-Pliocene period. Passing on to the Proboscidea, we find three species of elephants and two of _Mastodon_ preserved in European beds of this period, all distinct from those of Post-Pliocene times. _Rodentia._--In this order we find representatives of many living European forms; as _Cricetus_ (hamster), _Arvicola_ (vole), _Castor_ (beaver), _Arctomys_ (marmot), _Hystrix_ (porcupine), _Lepus_ (hare), and _Lagomys_ (pika); and a few that are extinct, the most important being _Chalicomys_, allied to the beaver; and _Issiodromys_, said to come nearest to the remarkable _Pedetes_ of South Africa, both found in the Pliocene formations of France. _General Conclusions as to Pliocene and Post-Pliocene Faunas of Europe._--This completes the series of fossil forms of the Pliocene deposits of Europe. They show us that the presence of numerous large carnivora and ungulates (now almost wholly tropical) in the Post-Pliocene period, was due to no exceptional or temporary cause, but was the result of a natural succession from similar races which had inhabited the same countries for long preceding ages. In order to understand the vast periods of time covered by the Pliocene and Post-Pliocene formations, the works of Sir Charles Lyell must be studied. We shall then come to see, that the present condition of the fauna of Europe is wholly new and exceptional. For a long succession of ages, various forms of monkeys, hyænas, lions, horses, hipparions, tapirs, rhinoceroses, hippopotami, elephants, mastodons, deer, and antelopes, together {114}with almost all the forms now living, produced a rich and varied fauna such as we now see only in the open country of tropical Africa. During all this period we have no reason to believe that the climate or other physical conditions of Europe were more favourable to the existence of these animals than now. We must look upon them, therefore, as true indigenes of the country, and their comparatively recent extinction or banishment as a remarkable phenomenon for which there must have been some adequate cause. What this cause was we can only conjecture; but it seems most probable that it was due to the combined action of the Glacial period, and the subsidence of large areas of land once connecting Europe with Africa. The existence, in the small island of Malta, of no less than three extinct species of elephant (two of very small stature), of a gigantic dormouse, an extinct hippopotamus, and other mammalia, together with the occurrence of remains of hippopotamus in the caves of Gibraltar, indicate very clearly that during the Pliocene epoch, and perhaps during a considerable part of the Post-Pliocene, a connection existed between South Europe and North Africa in at least these two localities. At the same time we have every reason to believe that Britain was united to the Continent, what is now the German Ocean constituting a great river-valley. During the height of the Glacial epoch, these large animals would probably retire into this Mediterranean land and into North Africa, making annual migrations northwards during the summer. But as the connecting land sank and became narrower and narrower, the migrating herds would diminish, and at last cease altogether; and when the glacial cold had passed away would be altogether prevented from returning to their former haunts. MIOCENE PERIOD. We now come to a period which was wonderfully rich in all forms of life, and of which the geological record is exceptionally complete. Various lacustrine, estuarine, and other deposits in Europe, North India, and North America, have furnished such a {115}vast number of remains of extinct mammalia, as to solve many zoological problems, and to throw great light on the early distribution and centres of dispersal of various groups of animals. In order to show the bearing of these remains on our special subject, we will first give an account of the extinct fauna of Greece, of the Upper Miocene period; since this, being nearest to Africa and Asia, best exhibits the relations of the old European fauna to those countries. We shall then pass to the Miocene fauna of France and Central Europe; and conclude with the remarkable Siwalik and other Indian extinct faunas, which throw an additional light on the early history of the animal life of the great old-world continents. _Extinct Animals of Greece._ These are from the Upper Miocene deposits at Pikermi, near Athens, and were collected by M. Gaudry a few years ago. They comprise ten living and eighteen extinct genera of mammalia, with a few birds and reptiles. _Primates._--These are represented by _Mesopithecus_, a genus believed to be intermediate between the two Indian genera of monkeys, _Semnopithecus_ and _Macacus_. _Carnivora._--These were abundant. Of _Felis_ there were four species, ranging from the size of a cat to that of a jaguar, a large _hyæna_, and a large weasel (_Mustela_). Besides these there were the huge _Machairodus_, larger than any existing lion or tiger, and with enormously developed canine teeth; _Hyænictis_ and _Lycæna_, extinct forms of Hyænidæ; _Thalassictis_=_Ictitherium_, an extinct genus of Viverridæ but with resemblances to the hyænas, represented by three species, some of which were larger than any existing Viverridæ; _Promephytis_, an extinct form of Mustelidæ, having resemblances to the European marten, to the otters, and to the S. African _Zorilla_; and lastly, _Simocyon_, an extraordinary carnivore of the size of a small panther, but having the canines of a cat, the molars of a dog, and the jaws shaped like those of a bear. _Ungulata._--These are numerous and very _interesting_. The Equidæ are represented by the three-toed _Hipparion_, which {116}continued to exist till the Older Pliocene period. There are three large species of _Rhinoceros_, as well as a species of the extinct genus _Leptodon_ of smaller size. Remains of a very large wild boar (_Sus_) were found. Very interesting is the occurrence of a species of giraffe (_Camelopardalis_) as tall as the African species but more slender; and also an extinct genus _Helladotherium_, not quite so tall as the giraffe but much more robust, and showing some approach to the Antilopidæ in its dentition. Antelopes were abundant, ranging from the size of the gazelle to that of the largest living species. Three or four seem referable to living genera, but the majority are of extinct types, and are classed in the genera _Palæotragus_, _Palæoryx_, _Tragocerus_, and _Palæoreas_; while _Dremotherium_ is an ancient generalized form of _Cervidæ_ or deer. _Proboscidea._--These are represented by two species of _Mastodon_, and two of _Dinotherium_, an extraordinary extinct form supposed to be, to some extent, intermediate between the elephants and the aquatic manatees (_Sirenia_.) _Rodentia._--This order is represented by a species of _Hystrix_, larger than living porcupines. _Edentata._--This order, now almost confined to South America, was represented in the Miocene period by several European species. _Ancylotherium_ and _Macrotherium_, belonging to an extinct family but remotely allied to the African ant-bear (_Orycteropus_), occur in Greece. _Birds._--Species of _Phasianus_ and _Gallus_ were found; the latter especially interesting as being now confined to India. _Reptiles._--These are few and unimportant, consisting of a tortoise (_Testudo_) and a large lizard allied to _Varanus_. _Summary of the Miocene Fauna of Greece._--Although we cannot consider that the preceding enumeration gives us by any means a complete view of the actual inhabitants of this part of Europe during the later portion of the Miocene period, we yet obtain some important information. The resemblance that appeared in the Pliocene fauna of Europe, to that of the open country of tropical Africa, is now still more remarkable. We {117}not only find great felines, surpassing in size and destructive power the lions and leopards of Africa, with hyænas of a size and in a variety not to be equalled now, but also huge rhinoceroses and elephants, two forms of giraffes, and a host of antelopes, which, from the sample here obtained, were probably quite as numerous and varied as they now are in Africa. Joined with this abundance of antelopes we have the absence of deer, which probably indicates that the country was open and somewhat of a desert character, since there were deer in other parts of Europe at this epoch. The occurrence of but a single species of monkey is also favourable to this view, since a well-wooded country would most likely have supplied many forms of these animals. _Miocene Fauna of Central and Western Europe._ We have now to consider the Miocene fauna of Europe generally, of which we have very full information from numerous deposits of this age in France, Switzerland, Italy, Germany, and Hungary. _Primates._--Three distinct forms of monkeys have been found in Europe--in the South of France, in Switzerland, and Wurtemberg; one was very like _Colobus_ or _Semnopithecus_; the others--_Pliopithecus_ and _Dryopithecus_--were of higher type, and belonged to the anthropomorphous apes, being nearest to the genus _Hylobates_ or gibbons. Both have occurred in the South of France. The _Dryopithecus_ was a very large animal (equal to the gorilla), and M. Lartet considers that in the character of its dentition it approached nearer to man than any of the existing anthropoid apes. _Insectivora._--These small animals are represented by numerous remains belonging to four families and a dozen genera. Of _Erinaceus_ (hedgehog) several species are found in the Upper Miocene; and in the Lower Miocene of Auvergne two extinct genera of the same family--_Amphechinus_ and _Tetracus_--have been discovered. Several species of _Talpa_ (mole) occur in the Upper Miocene of France, while the extinct _Dinylus_ is from Germany, and _Palæospalax_ from the Lower Miocene of the Isle of {118}Wight. The Malayan family Tupaiidæ or squirrel-shrews, is believed to be represented by _Oxygomphus_, a fossil discovered in South Germany (Wiesenau) by H. von Meyer. The Soricidæ or shrews, are represented by several extinct genera--_Plesiosorex_, _Mysarachne_ and _Galeospalax_; as well as by _Amphisorex_ and _Myogale_ still living. _Echinogale_, a genus of Centetidæ now confined to Madagascar, is said to occur in the Lower Miocene of Auvergne, a most interesting determination, if correct, as it would form a transition to the _Solenodon_ of the Antilles belonging to the same family; but I am informed by Prof. Flower that the affinities of the animals described under this name are very doubtful. _Carnivora._--Besides _Felis_ and _Machairodus_, which extend back to the Upper Miocene, there are two other genera of Felidæ, _Pseudælurus_ in the Upper Miocene of France, and _Hyænodon_, which occurs in the Upper and Lower Miocene of France, named from some resemblance in its teeth to the hyænas, and considered by some Palæontologists to form a distinct family, Hyænodontidæ. The Viverridæ, or civets, were very numerous, consisting of the living genus _Viverra_, and three extinct forms--_Thalassictis_=_Ictitherium_, as large as a panther, and _Soricictis_, a smaller form, occurring both in France and Hungary. Of _Hyænidæ_, there was the living genus _Hyæna_, and the extinct _Hyænictis_, which has occurred in Hungary as well as in Greece. The Canidæ, or wolf and fox family, were represented by _Pseudocyon_, near to _Canis_; _Hemicyon_, intermediate between dogs and gluttons; and _Amphicyon_, of which several species occur in the Upper and Lower Miocene of France, some of them larger than a tiger. The Mustelidæ, or weasels, were represented by five genera, the existing genera _Lutra_ (otter) and _Mustela_ (weasel); _Potamotherium_, an extinct form of otter; _Taxodon_, allied to the badger and otter; _Palæomephitis_ in Germany, and the _Promephytis_ (already noticed) in Greece. The bears were represented only by _Hyænarctos_, which has been noticed as occurring in the Pliocene, and first appears in the Upper Miocene of France. Seals are represented by a form resembling the Antarctic _Otaria_, remains of which occur in the Upper Miocene of France. {119}_Cetacea_ (whales).--These occur frequently in the Miocene deposits, four living, and five extinct genera having been described; but these marine forms are not of much importance for our purpose. _Sirenia_ (sea-cows).--These are represented by two extinct genera, _Halitherium_ and _Trachytherium_. Several species of the former have been discovered, but the latter has occurred in France only, and its affinities are doubtful. _Ungulata._--Horses are represented by _Hipparion_ and _Anchitherium_, the latter occurring in both Upper and Lower Miocene and Eocene; while _Hipparion_, which is more nearly allied to living horses, first appears in the Upper Miocene and continues in the Pliocene. _Hippotherium_, in the Upper Miocene of the Vienna basin, forms a transition to _Paloplotherium_, an Eocene genus of Tapiridæ or Palæotheridæ. Tapirs, allied to living forms, occur in both Upper and Lower Miocene. Rhinoceroses are still found in the Upper Miocene, and here first appear the four-toed hornless rhinoceros, _Acerotherium_. The Suidæ (swine) are rather numerous. _Sus_ (wild boar) continued as far back as the Upper Miocene; but now there first appear a number of extinct forms which have been named _Hyotherium_, _Palæochoerus_, _Choeromorus_, all of a small or moderate size; _Hyopotamus_, nearly as large as a tapir; and _Anthracotherium_, nearly the size of a hippopotamus and, according to Dr. Leidy, the type of a distinct family. _Listriodon_, from the Upper Miocene of the Vienna basin, is sometimes classed with the tapirs. We now come to a well-marked new family of Artiodactyle or even-toed Ungulata, the _Anoplotheriidæ_, which consisted of more slender long-tailed animals, allied to the swine but with indications of a transition towards the camels. The only genera that appear in the Miocene formation are, _Chalicotherium_, nearly as large as a rhinoceros, of which three species have been found in Germany and France; and _Synaphodus_, known only from its teeth, which differ somewhat from those of the _Anoplotherium_ which appears earlier in the Eocene formation. Another extinct family, _Amphimericidæ_ or _Xiphodontidæ_, is represented by two {120}genera, _Cainotherium_ and _Microtherium_, in the Miocene of France. They were of very small size, and are supposed to be intermediate between the Suidæ and Tragulidæ. The Camelopardalidæ, or giraffes, were represented in Europe in Miocene times by the gigantic _Helladotherium_, which has been found in the south of France, and in Hungary, as well as in Greece. The chevrotains (Tragulidæ) are represented by the extinct genus _Hyomoschus_. The Cervidæ do not seem to have appeared in Europe before the Upper Miocene epoch, when they were represented by _Dorcatherium_ and _Amphimoschus_, allied to _Moschus_, and also by true _Cervus_, as well as by small allied forms, _Dremotherium_, _Amphitragalus_ (in the Lower Miocene), _Micromeryx_, _Palæomeryx_, and _Dicrocerus_. The Bovidæ, or hollow-horned ruminants, were not well represented in Central Europe in Miocene times. There were no sheep, goats, or oxen, and only a few antelopes of the genus _Tragocerus_, and one allied to _Hippotragus_; and these all lived in the Upper Miocene period, as did the more numerous forms of Greece. _Proboscidea._--The true elephants do not extend back to the Miocene period, but they are represented by the Mastodons, which had less complex teeth. These first appear in the Upper Miocene of Europe, five species being known from France, Germany, Switzerland, and Greece. _Dinotherium_, already noticed as occurring in Greece, extended also to Germany and France, where remains of three species have been found. _Rodentia._--A considerable number of generic forms of this order have been obtained from the Miocene strata. The principal genera are _Cricetodon_, allied to the hamsters, numerous in both the Upper and Lower Miocene period of France; _Myoxus_ (the dormice) in France, and an allied genus, _Brachymys_, in Germany. The beavers were represented by the still living genus _Castor_, and the extinct _Steneofiber_ in France. The squirrels by the existing _Scuirus_ and _Spermophilus_; and by extinct forms, _Lithomys_ and _Aulacodon_, in Germany, the latter resembling the African genus _Aulacodes_. The hares, by _Lagomys_ and an {121}extinct form _Titanomys_. Besides these, remains referred to the South American genera, _Cavia_ (cavy) and _Dasyprocta_ (agouti), have been found, the former in the Upper Miocene of Switzerland, the latter in the Lower Miocene of Auvergne. _Palæomys_, allied to the West Indian _Capromys_, has been found in the same deposits; as well as _Theridomys_, said by Gervais to be allied to _Anomalurus_ and _Echimys_, the former now living in W. Africa, the latter in S. America. _Edentata._--These are only represented by the _Macrotherium_ and _Ancylotherium_ of the Grecian deposits, the former occurring also in France and Germany in Upper Miocene strata. _Marsupials_.--These consist of numerous species related to the opossums (_Didelphys_), but separated by Gervais under the name _Peratherium_. They occur in both Upper and Lower Miocene beds. _Upper Miocene Deposits of the Siwalik Hills and other Localities in N. W. India._ These remarkable fresh-water deposits form a range of hills at the foot of the Himalayas, a little south of Simla. They were investigated for many years by Sir P. Cautley and Dr. Falconer, and add greatly to our knowledge of the early fauna of the Old World continent. _Primates_.--Remains of the genera _Semnopithecus_ and _Macacus_ were found, with other forms of intermediate character; and some teeth indicated animals allied to the orang-utan of Borneo, and of similar size. _Carnivora_.--These consisted of species of _Felis_ and _Machairodus_ of large size; _Hyæna_, _Canis_, _Mellivora_, and an allied genus _Ursitaxus_; _Ursus_, in the deposits of the Nerbudda valley (of Pliocene age); _Hyænarctos_ as large as the cave bear; _Amphicyon_ of the size of a polar bear (in the deposits of the Indus valley, west of Cashmere); _Lutra_, and an extinct allied genus _Enhydrion_. _Ungulata_.--These are very numerous, and constitute the most important feature of this ancient fauna. Horses are represented by a species of _Equus_ from the Siwalik Hills and the Irawaddy {122}deposits in Burmah, and by two others from the Pliocene of the Nerbudda Valley; while _Hippotherium_--a slender, antelope-like animal, found in the Siwalik Hills and in Europe--is supposed to form a transition from the Equidæ to the Tapiridæ. These latter are found in the Upper Indus deposits, where there is a species of _Tapirus_, and one of an extinct genus _Antelotherium_. Of _Rhinoceros_, five extinct species have been found--in the Siwalik Hills, in Perim Island, and one at an elevation of 16,000 feet in the deserts of Thibet. _Hippopotamus_ occurs in the Pliocene of the Nerbudda, and is represented in the older Miocene deposits by _Hexaprotodon_, of which three species have been found in various parts of India. Another remarkable genus, _Merycopotamus_, connects _Hippopotamus_ with _Anthracotherium_, one of the extinct European forms allied to the swine. These last are represented by several large species of _Sus_, and by the extinct European genus _Choerotherium_. The extinct Anoplotheridæ are represented by a species of the European genus _Chalicotherium_, larger than a horse. An extinct camel, larger than the living species, was found in the Siwalik Hills. Three species of deer (_Cervus_) have been found in the Siwaliks, and one in the Nerbudda deposits. A large and a small species of giraffe (_Camelopardalis_) were found in the Siwalik Hills and at Perim Island. The Bovidæ are represented by numerous species of _Bos_, and by the extinct genera _Hemibos_ and _Amphibos_. There are also three species of antelopes, one of which is allied to the African _Alcephalus_. We now come to an extraordinary group of extinct animals, probably forming a new family intermediate between the antelope and the giraffe. The _Sivatherium_ was an enormous four-horned ruminant, larger than a rhinoceros. It had a short trunk like a tapir, the lower horns on the forehead were simple, the upper pair palmated. The _Bramatherium_, an allied form from Perim Island, showed somewhat more affinity for the giraffe. _Proboscidea._--No less than seven species of elephants and four {123}of mastodons ranged over India, their remains being found in all the deposits from the Siwalik Hills to Burmah. A large _Dinotherium_ has also been found at Perim Island. _Reptiles._--Many remains of birds were found, but these have not been determined. Reptiles were numerous and interesting, the most remarkable being the huge tortoise, _Colossochelys_, whose shell was twelve feet long and head and neck eight feet more. Other small tortoises of the genera _Testudo_, _Emys_, _Trionyx_ and _Emydida_ were found, the Emys being a living species. There were three extinct and one living species of crocodile, and one of them was larger than any now living. The only other reptile of importance was a large lizard of the genus _Varanus_. _General Observations on the Miocene faunas of Europe and Asia._--Comparing the three faunas of approximately the same period, and allowing for the necessarily imperfect record of each, we find a wonderful similarity of general type over the enormous area between France on the west and the Irawaddy river in Burmah on the east. We may even extend our comparison to Northern China, where remains of _Hyæna_, _Tapir_, _Rhinoceros_, _Chalicotherium_, and _Elephas_, have been recently found, closely resembling those from the Miocene or Pliocene deposits of Europe or India, and showing that the Palæarctic region had then the same great extent from west to east that it has now. Of about forty genera comprised in the Indian Miocene fauna, no less than twenty-seven inhabited Central and Western Europe during the same epoch. The Indian Miocene fossils are much what we should expect as the forerunners of the existing fauna, the giraffes and hippopotami being the only additions from the present Ethiopian fauna. The numerous forms of the restricted bovine type, show that these probably originated in India; while the monkeys appear to be altogether of Oriental types. In Europe, however, we meet with a totally different assemblage of animals from those that form the existing fauna. We find apes and monkeys, many large Felidæ, numerous civets {124}and hyænas, tapirs, rhinoceros, hippopotamus, elephants, giraffes, and antelopes, such as now characterise the tropics of Africa and Asia. Along with these we meet with less familiar types, showing relations with the Centetidæ of Madagascar, the Tupaiidæ of the Malay Islands, the _Capromys_, of the West Indies, and the _Echimys_ of South America. And besides all these living types we have a host of extinct forms,--ten or twelve genera allied to swine; nine genera of tapir-like animals; four of horses; nine of wolves; with many distinct forms of the long-extinct families of Anoplotheridæ, Xiphodontidæ, and the edentate Macrotheridæ. It is almost certain that during the Miocene period Europe was not only far richer than it is now in the higher forms of life, but not improbably richer than any part of the globe now is, not excepting tropical Africa and tropical Asia. EOCENE PERIOD. The deposits of Eocene age are less numerous, and spread over a far more limited area, than those of the Miocene period, and only restricted portions of them furnish any remains of land animals. Our knowledge of the Eocene mammalian fauna is therefore very imperfect and will not occupy us long, as most of the new types it furnishes are of more interest to the zoologist than to the student of distribution. Some of the Eocene mammalia of Europe are, however, of interest in comparison with those of North America of the same age; while others show that ancestral types of groups now confined to Australia or to South America, then inhabited Europe. _Primates._--The only undoubted Eocene examples of this order, are the _Cænopithecus lemuroides_ from the Jura, which has points of resemblance to the South American marmosets and howlers, and also to the Lemuridæ; and a cranium recently discovered in the Department of Lot (S.W. France), undoubtedly belonging to the Lemuridæ, and which most resembles that of the West African "Potto" (_Perodicticus_). This discovery has led to another, for it is now believed that remains formerly {125}referred to the Anoplotheridæ (_Adapis_ and _Aphelotherium_ from the Upper Eocene of Paris) were also Lemurs. Some remains from the Lower Eocene of Suffolk were at first supposed to be allied to _Macacus_, but were subsequently referred to the Ungulate, _Hyracotherium_. There is still, however, some doubt as to its true affinities. _Chiroptera._--In the Upper Eocene of Paris remains of bats have been found, so closely resembling living forms as to be referred to the genus _Vespertilio_. _Carnivora._--The only feline remains, are those of _Hyænodon_ in the Upper Eocene of Hampshire, and _Pterodon_, an allied form from beds of the same age in France; with _Ælurogale_, found in the South of France in deposits of phosphate of lime of uncertain age, but probably belonging to this period. Viverridæ (civets) are represented by two genera, _Tylodon_, the size of a glutton from the Upper Eocene, and _Palæonyctis_, allied to _Viverra_, from the Middle Eocene of France. The Canidæ (wolves and foxes) appear to have been the most ancient of the existing types of Carnivora, five genera being represented by Eocene remains. Of these, _Galethylax_ and _Cyotherium_ were small, and with the existing genus _Canis_ are found in the Upper Eocene of France. _Arctocyon_, about the size of a wolf, is a very ancient and generalised form of carnivore which can not be placed in any existing family. It is found in the Lower Eocene of France, and is thus the oldest known member of the Carnivora. _Ungulata._--These are more numerous. Equidæ (horses) are represented by the Miocene _Anchitherium_ in the Lower, and by a more ancient form, _Anchilophus_, in the Middle Eocene of France. Tapiridæ and Palæotheridæ were very numerous. _Palæotherium_ and the allied genus _Paloplotherium_, were abundant in France and England in Upper Eocene times. They somewhat resembled the tapir, with affinities for the horse and rhinoceros. A new genus, _Cadurcotherium_, allied to the rhinoceros and equally large, has been found in the same deposits of phosphate of lime as the lemur and _Ælurogale_. In the Middle Eocene of both England and France are found _Lophiodon_ allied to the tapir, {126}but in some of the species reaching a larger size; _Propalæotherium_ and _Pachynolophus_ of smaller size and having affinities for the other genera named; and _Plagiolophus_, a small, slender animal which Professor Huxley thinks may have been a direct ancestor of the horse. In the Lower Eocene we meet with _Coryphodon_, much larger than the tapir, and armed with large canine teeth; _Pliolophus_, a generalised type, allied to the tapir and horse; and _Hyracotherium_, a small animal from the Lower Eocene of England, remotely allied to the tapir. Among the Artiodactyla, or even-toed ungulates, the swine are represented by several extinct genera, of moderate or small size--_Acotherium_, _Choeropotamus_, _Cebochoerus_ and _Dichobune_, all from the Upper and the last also from the Middle Eocene of France; but _Eutelodon_, from the phosphate of lime deposits is large. The _Dichobune_ was the most generalised type, presenting the characters of many of the other genera combined, and was believed by Dr. Falconer to approach the musk-deer. The _Cainotherium_ of the Miocene also occurs here, and an allied genus _Plesiomeryx_ from the same deposits as _Euteledon_. The Eocene Anoplotheridæ were numerous. The _Anoplotherium_ was a two-toed, long-tailed Pachyderm, ranging from the size of a hog to that of an ass; the allied _Eurytherium_ was four-toed; and there are one or two others of doubtful affinity. All are from the Upper Eocene of France and England. _Rodentia._--Remains referred to the genera _Myoxus_ (dormouse) and _Sciurus_ (squirrel) have been found in the Upper Eocene of France; as well as _Plesiarctomys_, an extinct genus between the marmots and squirrels. The Miocene _Theridomys_ is also found here. _Marsupials._--The _Didelphys_ (opossum) of Cuvier, now referred to an extinct genus _Peratherium_, is found in the Upper Eocene of France and England. _General Considerations on the Extinct Mammalian Fauna of Europe._--It is a curious fact that no family, and hardly a genus, of European mammalia occurs in the Pliocene deposits, without extending back also into those of Miocene age. There are, {127}however, a few groups which, seem to be late developments or recent importations into the Palæarctic region, as they occur only in Post-Pliocene deposits. The most important of these are the badger, glutton, elk, reindeer, chamois, goat, and sheep, which only occur in caves and other deposits of Post-Pliocene age. Camels only occur in the Post-Pliocene of Siberia (_Merycotherium_), although a true _Camelus_ of large size appears to have inhabited some part of Central Asia in the Upper Miocene period, being found in the Siwalik beds. The only exclusively Pliocene genera in Europe are _Ursus_, _Equus_, _Hippopotamus_, _Bos_, _Elephas_, _Arvicola_, _Trogontherium_, _Arctomys_, _Hystrix_ and _Lepus_; but of these _Equus_, _Hippopotamus_, _Bos_, and _Elephas_ are found in the Miocene deposits of India. Owing, no doubt, in part to the superior productiveness of the various Miocene beds, large numbers of groups appear to have their origin or earliest appearance here. Such are Insectivora, Felidæ, Hyænidæ, Mustelidæ, _Ursus_, Equidæ, _Tapirus_, Rhinocerotidæ, Hippopotamidæ, Anthracotheridæ (extinct), _Sus_, Camelopardidæ, Tragulidæ, Cervidæ, Bovidæ, Elephantidæ, and Edentata. Groups which go back to the Eocene period, are, Primates allied to South American monkeys, as well as some of the Lemuridæ; bats of the living genus _Vespertilio_; Hyænodontidæ, an ancestral form of Carnivore; Viverridæ; Canidæ (to the Upper Eocene), and the ancestral Arctocyonidæ to the Lower Eocene; _Hyænarctos_, an ancestral type of bears and hyænas; Anchitheridæ, ancestral horses, to the Middle Eocene; Palæotheridæ, comprising numerous generalised forms, ancestors of the rhinoceros, horse, and tapir; Suidæ, with numerous generalised forms, to the Middle Eocene; Anoplotheridæ and Xiphodontidæ, ancestral families of even-toed Ungulates, connecting the ruminants with the swine; and lastly, several groups of Rodents, and a Marsupial, in the Upper Eocene. We thus find all the great types of Mammalia well developed in the earliest portion of the tertiary period; and the occurrence of Quadrumana, of the highly specialized bats (_Vespertilio_), of various forms of Carnivora, and of Ungulates, clearly differentiated into the odd and even-toed series, associated with such lower forms as {128}Lemurs and Marsupials--proves, that we have here hardly made an approach towards the epoch when the mammalian type itself began to diverge into its various modifications. Some of the Carnivora and Ungulates do, indeed, exhibit a less specialised structure than later forms; yet so far back as the Upper Miocene the most specialised of all carnivora, the great sabre-toothed _Machairodus_, makes its appearance. The Miocene is, for our special study, the most valuable and instructive of the Tertiary periods, both on account of its superior richness, and because we here meet with many types now confined to separate regions. Such facts as the occurrence in Europe during this period of hippopotami, tapirs, giraffes, Tragulidæ, Edentata, and Marsupials--will assist us in solving many of the problems we shall meet with in reviewing the actual distribution of living forms of those groups. Still more light will, however, be thrown on the subject by the fossil forms of the American continent, which we will now proceed to examine. {129}CHAPTER VII. EXTINCT MAMMALIA OF THE NEW WORLD. The discoveries of very rich deposits of mammalian remains in various parts of the United States have thrown great light on the relations of the faunas of very distant regions. North America now makes a near approach to Europe in the number and variety of its extinct mammalia, and in no part of the world have such perfect specimens been discovered. In what are called the "Mauvaises terres" of Nebraska (the dried-up mud of an ancient lake), thousands of entire crania and some almost entire skeletons of ancient animals have been found, their teeth absolutely perfect, and altogether more resembling the preparations of the anatomist, than time-worn fossils such as we are accustomed to see in the museums of Europe. Other deposits have been discovered in Oregon, California, Virginia, South Carolina, Texas, and Utah, ranging over all the Tertiary epochs, from Post-Pliocene to Eocene, and furnishing a remarkable picture of the numerous strange mammalia which inhabited the ancient North American continent. NORTH AMERICA--POST-PLIOCENE PERIOD. _Insectivora._--The only indications of this order yet discovered, consists of a single tooth of some insectivorous animal found in Illinois, but which cannot be referred to any known group. _Carnivora._--These are fairly represented. Two species of _Felis_ as large as a lion; the equally large extinct _Trucifelis_, found only in Texas; four species of _Canis_, some of them larger {130}than wolves; two species of _Galera_, a genus now confined to the Neotropical region; two bears, and an extinct genus, _Arctodus_; an extinct species of racoon (_Procyon_), and an allied extinct genus, _Myxophagus_--show, that at a very recent period North America was better supplied with Carnivora than it is now. Remains of the walrus (_Trichechus_) have also been found as far south as Virginia. _Cetacea._--Three species of dolphins belonging to existing genera, have been found in the Eastern States; and two species of _Manatus_, or sea-cow, in Florida and South Carolina. _Ungulata._--Six extinct horses (_Equus_), and one _Hipparion_; the living South American tapir, and a larger extinct species; a _Dicotyles_, or peccary, and an allied genus, _Platygonus_; a species of the South American llamas (_Auchenia_), and one of a kind of camel, _Procamelus_; two extinct bisons; a sheep, and two musk-sheep (_Ovibos_); with three living and one extinct deer (_Cervus_), show an important increase in its Herbivora. _Proboscidea._--Two elephants and two mastodons, added to this remarkable assemblage of large vegetable-feeding quadrupeds. _Rodentia._--These consist mainly of genera and species still living in North America; the only important exceptions being a species of the South American capybara (_Hydrochoerus_) in South Carolina; and _Praotherium_, an extinct form of hare, found in a bone cave in Pennsylvania. _Edentata._--Here we meet with a wonderful assemblage, of six species belonging to four extinct genera, mostly of gigantic size. A species of _Megatherium_, three of _Megalonyx_, and one of _Mylodon_--huge terrestrial sloths as large as the rhinoceros or even as the largest elephants--ranged over the Southern States to Pennsylvania, the latter (_Mylodon_) going as far as the great lakes and Oregon. Another form, _Ereptodon_, has been found in the Mississippi Valley. _Marsupialia._--The living American genus of opossums, _Didelphys_, has been found in deposits of this age in South Carolina. _Remarks on the Post-Pliocene fauna of North America._--The assemblage of animals proved, by these remains, to have {131}inhabited North America at a comparatively recent epoch, is most remarkable. In Europe, we found a striking change in the fauna at the same period; but that consisted almost wholly in the presence of animals now inhabiting countries immediately to the north or south. Here we have the appearance of two new assemblages of animals, the one now confined to the Old World--horses, camels, and elephants; the other exclusively of South American type--llamas, tapirs, capybaras, _Galera_, and gigantic Edentata. The age of the various deposits in which these remains are found is somewhat uncertain, and probably extends over a considerable period of time, inclusive of the Glacial epoch, and perhaps both anterior and subsequent to it. We have here, as in Europe, the presence and apparent co-existence in the same area, of Arctic and Southern forms--the walrus and the manatee--the musk-sheep and the gigantic sloths. Unfortunately, as we shall see, the immediately preceding Pliocene deposits of North America are rather poor in organic remains; yet it can hardly be owing to the imperfection of the record of this period, that _not one_ of the South American types above numerated occurs there, while a considerable number of Old World forms are represented. Neither in the preceding wonderfully rich Miocene or Eocene periods, does any _one_ of these forms occur; or, with the exception of _Morotherium_, from Pliocene deposits _west_ of the Rocky Mountains, any apparent ancestor of them! We have here unmistakable evidence of an extensive immigration from South into North America, not very long before the beginning of the Glacial epoch. It was an immigration of types altogether new to the country, which spread over all the southern and central portions of it, and established themselves sufficiently to leave abundance of remains in the few detached localities where they have been discovered. How such large yet defenceless animals as tapirs and great terrestrial sloths, could have made their way into a country abounding in large felines equal in size and destructiveness to the lion and the tiger, with numerous wolves and bears of the largest size, is a great mystery. But it is nevertheless certain that they did so; and the fact that no such {132}migration had occurred for countless preceding ages, proves that some great barrier to the entrance of terrestrial mammalia which had previously existed, must for a time have been removed. We must defer further discussion of this subject till we have examined the relations of the existing faunas of North and South America. TERTIARY PERIOD. When we get to remains of the Tertiary age, especially those of the Miocene and Eocene epochs, we meet with so many interesting and connected types, and such curious relations with living forms in Europe, that it will be clearer to trace the history of each order and family throughout the Tertiary period, instead of considering each of the subdivisions of that period separately. It will be well however first to note the few American Post-Pliocene or living genera that are found in the Pliocene beds. These consist of several species of _Canis_, from the size of a fox to that of a large wolf; a _Felis_ as large as a tiger; an Otter (_Lutra_); several species of _Hipparion_; a peccary (_Dicotyles_); a deer (_Cervus_); several species of _Procamelus_; a mastodon; an elephant; and a beaver (_Castor_). It thus appears that out of nearly forty genera found in the Post-Pliocene deposits, only ten are found in the preceding Pliocene period. About twelve additional genera, however, appear there, as we shall see in going over the various orders. _Primates._--Among the vast number of extinct mammalia discovered in the Tertiary deposits of North America, no example of this order had been recognized up to 1872, when the discovery of more perfect remains showed, that a number of small animals of obscure affinities from the Lower Eocene of Wyoming, were really allied to the lemurs and perhaps also to the marmosets, the lowest form of American monkeys, but having a larger number of teeth than either. A number of other remains of small animals from the same formation, previously supposed to be allied to the Ungulata, are now shown to {133}belong to the Primates; so that no less than twelve genera of these animals are recognized by Mr. Marsh, who classes them in two families--Limnotheridæ, comprising the genera _Limnotherium_, (which had larger canine teeth), _Thinolestes_, _Telmatolestes_, _Mesacodon_, _Bathrodon_, and _Antiacodon_ of Marsh, with _Notharctos_, _Hipposyus_, _Microsyops_, and _Palæacodon_ previously described by Leidy;--and Lemuravidæ, consisting of the genera _Lemuravus_ (Marsh) and _Hyopsodus_ (Leidy). The animals of the latter family were most allied to existing lemurs, but were a more generalized form, _Lemuravus_ having forty-four teeth, the greatest number known in the order. These numerous forms ranged from the size of a small squirrel to that of a racoon. It is especially interesting to find these peculiar lemuroid forms in America, just when a lemur has been discovered of about the same age in Europe; and as the American forms are said to show an affinity with the South American marmosets, while the European animal is most allied to a West African group, we have evidently not yet got back far enough to find the primeval or ancestral type from which all the Primates sprang. About the same time, in the succeeding Miocene formation, true monkeys were discovered. Mr. Marsh describes _Laopithecus_ as an animal nearly the size of the largest South American monkeys, and allied both to the Cebidæ and the Eocene Limnotheridæ. Mr. Cope has described _Menotherium_ from the Miocene of Colorado, as a lemuroid animal, the size of a cat, and perhaps allied to _Limnotherium_. More Miocene remains will, no doubt, be discovered, by which we shall be enabled to trace the origin of some of the existing forms of South American monkeys; and perhaps help to decide the question (now in dispute among anatomists) whether the lemurs are really Primates, or form an altogether distinct and isolated order of mammalia. _Insectivora._--This order is represented by comparatively few forms in the tertiary beds, and these are all very different from existing types. In the Upper Miocene of Dakota are found remains indicating two extinct genera, _Lepictis_ and _Ictops_. In the Miocene of Colorado, Professor Cope has recently discovered four new genera, _Isacis_; allied to the preceding, but as large as a {134}_Mephitis_ or skunk; _Herpetotherium_, near the moles; _Embasis_, more allied to the shrews; and _Dommina_, of uncertain affinities. Two others have been found in the Eocene of Wyoming; _Amomys_, having some resemblance to hedgehogs and to the Eastern _Tupaia_; and _Washakius_, of doubtful affinities. Far back in the Triassic coal of North Carolina has been found the jaw of a small mammal (_Dromotherium_), the teeth of which somewhat resemble those of the Australian _Myrmecobius_, and may belong either to the Insectivora or Marsupials; if indeed, at that early period these orders were differentiated. _Carnivora._--The most ancient forms of this order are some remains found in the Middle Eocene of Wyoming, and others recently described by Professor Cope (1875) from the Eocene of New Mexico, of perhaps earlier date. The former consist of three genera, _Patriofelis_, _Uintacyon_, and _Sinopa_,--animals of large size but which cannot be classed in any existing family; and two others, _Mesonyx_ and _Synoplotherium_, believed by Mr. Cope to be allied to _Hyænodon_. The latter consist of four genera,-- _Oxyæna_, consisting of several species, some as large as a jaguar, was allied to _Hyænodon_ and _Pterodon_; _Pachyæna_, allied to the last; _Prototomus_, allied to _Amphicyon_ and the Viverridæ; and _Limnocyon_, a civet-like carnivore with resemblances to the Canidæ. In the Miocene formations we find the Feline type well developed. The wonderful _Machairodus_, which in Europe lived down to Post-Pliocene times, is found in the Upper Miocene of Dakota; and perfect crania have been discovered, showing that the chin was lengthened downwards to receive and protect the enormous canines. _Dinyctis_ was allied both to _Machairodus_ and to the weasels. Three new genera have been lately described by Professor Cope from the Miocene of Colorado,--_Bunælurus_, with characters of both cats and weasels; _Daptophilus_, allied to _Dinyctis_; and _Hoplophoneus_, more allied to _Machairodus_. The Canidæ are represented by _Amphicyon_, which occurs in deposits of the same age in Europe; and by _Canis_, four species of which genus are recorded by Professor Cope from the Miocene of Colorado, and it also occurs in the Pliocene. The _Hyænodon_ is represented by three species in the Miocene of Dakota and Colorado. It occurs {135}also in the European Miocene and Upper Eocene formations, and constitutes a distinct family Hyænodontidæ, allied, according to Dr. Leidy, to wolves, cats, hyænas and weasels. The Ursidæ are represented by only one species of an extinct genus, _Leptarchus_, from the Pliocene of Nebraska. From the Pliocene of Colorado, Prof. Cope has recently described _Tomarctos_, as a "short-faced type of dog;" well as species of _Canis_ and _Martes_. _Ungulata._--The animals belonging to this order being usually of large size and accustomed to feed and travel in herds, are liable to wholesale destruction by floods, bogs, precipices, drought or hunger. It is for these reasons, probably, that their remains are almost always more numerous than those of other orders of mammalia. In America they are especially abundant; and the number of new and intermediate types about whose position there is much difference of opinion among Palæontologists, renders it very difficult to give a connected summary of them with any approach to systematic accuracy. Beginning with the Perissodactyla, or odd-toed ungulates, we find the Equine animals remarkably numerous and interesting. The true horses of the genus _Equus_, so abundant in the Post-Pliocene formations, are represented in the Pliocene by several ancestral forms. The most nearly allied to _Equus_ is _Pliohippus_, consisting of animals about the size of an ass, with the lateral toes not externally developed, but with some differences of dentition. Next come _Protohippus_ and _Hipparion_, in which the lateral toes are developed but are small and functionless. Then we have the allied genera, _Anchippus_, _Merychippus_, and _Hyohippus_, related to the European _Hippotherium_, which were all still smaller animals, _Protohippus_ being only 2½ feet high. In the older deposits we come to a series of forms, still unmistakably equine, but with three or more toes used for locomotion and with numerous differentiations in form, proportions, and dentition. These constitute the family Anchitheridæ. In the Miocene we have the genera _Anchitherium_ (found also in the European Miocene), _Miohippus_ and _Mesohippus_, all with three toes on each foot, and about the size of a sheep or large goat. In the Eocene of {136}Utah and Wyoming, we get a step further back, several species having been discovered about the size of a fox with four toes in front and three behind. These form the genus _Orohippus_, and are the oldest ancestral horse known. Prof. Marsh points out the remarkably perfect series of forms in America, which, beginning with this minute ancient type, is gradually modified by gaining increased size, increased speed by concentration of the limb-bones, elongation of the head and neck, the canine teeth decreased in size, the molars becoming longer and being coated with cement--till we at last come to animals hardly distinguishable, specifically, from the living horse. Allied to these, are a series of forms showing a transition to the tapirs, and to the _Palæotherium_ of the European Eocene. In the Pliocene we have _Parahippus_; in the Miocene _Lophiodon_, found in the same formation and in the Eocene of Europe, and allied to the tapir; and in the Eocene, _Palæosyops_, as large as a rhinoceros, which had large canines and was allied to the tapir and _Palæotherium_; _Limnohyus_, forming the type of a family Limnohyidæ, which included the last genus and some others mentioned further on; and _Hyrachyus_, allied to _Lophiodon_, and to _Hyracodon_ an extinct form of rhinoceros. Besides these we have _Lophiotherium_ (also from the Eocene of Europe); _Diplacodon_ allied to _Limnohyus_, but with affinities to modern Perissodactyla and nearly as large as a rhinoceros; and _Colonoceras_, also belonging to the Limnohyidæ, an animal which was the size of a sheep, and had divergent protuberances or horns on its nose. A remarkable genus, _Bathmodon_, lately described by Professor Cope, and of which five species have been found in the Eocene of New Mexico and Wyoming, is believed to form the type of a new family, having some affinity to _Palæosyops_ and to the extinct Brontotheridæ. It had large canine tusks but no horns. The Rhinocerotidæ are represented in America by the genus _Rhinoceros_ in the Pliocene and Miocene, and by _Aceratherium_ and _Hyracodon_ in the Miocene. Both the latter were hornless, and _Hyracodon_ was allied to the Eocene _Hyrachyus_, one of the Lophiodontidæ. In the Eocene and Miocene deposits of Utah, and Oregon, several remarkable extinct rhinoceroses have been {137}recently discovered, forming the genus _Diceratherium_. These had a pair of nasal horns placed side by side on the snout, not behind each other as in existing two-horned rhinoceroses, the rest of their skeleton resembling the hornless _Aceratherium_. They were of rather small size. Next to these extinct rhinoceroses come the Brontotheridæ, an extraordinary family of large mammalia, some of which exceeded in bulk the largest living rhinoceros. They had four toes to the front and three to the hind feet, with a pair of large divergent horns on the front of the head, in both sexes. Professor Marsh and Dr. Leidy have described four genera, _Brontotherium_, _Titanotheium_, _Megacerops_, and _Anisacodon_, distinguished by peculiarities of dentition. Though most nearly allied to the rhinoceroses, they show some affinity for the gigantic Dinocerata of the Eocene to be noticed further on. Professor Cope has since described another genus, _Symborodon_, from the Miocene of Colorado, with no less than seven species, one nearly the size of an elephant. He thinks they had a short tapir-like proboscis. The species differ greatly in the form of the cranium and development of the horn-bearing processes. We commence the Artiodactyla, or even-toed Ungulates, with the hog tribe. These are represented by species of peccaries, (_Dicotyles_) from the Pliocene of Nebraska and Oregon; and by an allied form _Thinohyus_, very like _Dicotyles_, but having an additional premolar tooth and a much smaller brain-cavity. From the Miocene are three allied genera, _Nanohyus_, _Leptochoerus_, and _Perchoerus_. Professor Cope, however, thinks _Leptochoerus_ may be Lemuroid, and allied to _Menotherium_. The Anthracotheridæ, a family which connects the Hippopotamidæ and Ruminants, and which occurs in the Miocene of Europe and India, are represented in America by the genus _Hyopotamus_ from the Miocene of Dakota, and _Elotherium_ from the Miocene of Oregon and the Eocene of Wyoming; the latter genus being sometimes classed with the preceding family, and lately placed by Professor Marsh, in the new order, Tillodontia. Professor Cope has since described three other genera from the Eocene of New {138}Mexico: _Meniscotherium_, having resemblances to _Palæosyops_, _Hyopotamus_, and the Limnotheridæ; _Phenacodus_, the size of a hog, of doubtful position, but perhaps near _Elotherium_; and _Achænodon_, as large as a cow, but more hog-like than the preceding. Another new genus from the Miocene of Colorado--_Pelonax_--is said by Professor Cope to come between _Elotherium_ and _Hippopotamus_. The Camelidæ are very abundant, and form one of the most striking features of the ancient fauna of America. _Procamelus_, _Homocamelus_, and _Megalomeryx_, are extinct genera found in the Pliocene formation; the first very closely allied to the Old World camel, the last smaller and more sheep-like. In the Miocene two other genera occur, _Poebrotherium_ and _Protomeryx_, the former allied to both the camel and the llama. Deer are represented by a single species of _Cervus_ in the Pliocene, while two extinct genera, _Leptomeryx_ and _Merycodus_, are found in the Miocene deposits, the latter indicating a transition between camels and deer. Two other genera, _Hypisodus_ and _Hypertragulus_, of very small size, are said by Professor Cope to be allied to the Tragulidæ and to _Leptomeryx_. The Bovidæ, or hollow-horned ruminants, are only represented in the Newer Pliocene by a single species of an extinct genus, _Casoryx_, said to be intermediate between antelopes and deer. We now come to an exclusively American family, the _Oreodontidæ_, which consisted of small animals termed by Dr. Leidy, "ruminating hogs," and which had some general structural resemblances to deer and camels. They abounded in North America during the Pliocene, and especially during the Miocene epoch, no less than six genera and twenty species having been discovered. _Merychus_ contains the Pliocene forms; while _Oreodon_, _Eporeodon_, _Merychochoerus_, _Leptauchenia_, and _Agriochoerus_ are Miocene. The last genus extends back into the Eocene period, and shows affinity to the European Anoplotheridæ of the same epoch. _Proboscidea._--The Elephantidæ are only represented in America by one species of _Mastodon_ and one of _Elephas_, in the Newer Pliocene deposits. In the Older Pliocene, Miocene, {139}and Upper Eocene, no remains of this order have been found; and in 1869, Dr. Leidy remarked on the small average size of the extinct North American mammalia, which were almost all smaller than their living analogues. Since then, however, wonderful discoveries have been made in deposits of Middle Eocene age in Wyoming and Colorado, of a group of huge animals not only rivalling the elephants in size, but of so remarkable and peculiar a structure as to require the formation of a new order of mammals--Dinocerata--for their reception. This order consists of animals with generalised Ungulate and Proboscidean affinities. The lower jaw resembles that of the hippopotamus; they had five toes on the anterior feet and four on the posterior; three pairs of horns, the first pair on the top of the head, large and perhaps palmated, the second pair above the eyes, while the third and smallest stood out sideways on the snout. They had enormous upper canines, of which the roots entered the middle horn cores, no upper incisors, and small molars. Professor Marsh believes that they had no trunk. The remains discovered indicate four genera, _Dinoceras_ (3 sp.), _Tinoceras_ (2 sp.), _Uintatherium_ (1 sp.), and _Eobasileus_ (2 sp.). Many other names have been given to fragments of these animals, and even those here given may not be all distinct. Another new order, Tillodontia, recently established by Professor Marsh, is perhaps yet more remarkable in a zoological point of view, since it combines the characters of Carnivora, Ungulata, and Rodents. These animals have been formed into two families, Tillotheridæ and Stylinodontidæ; and three genera, _Tillotherium_, _Anchippodus_, and _Stylinodontia_. All are from the Eocene of Wyoming and New Jersey. Perhaps to these must be added _Elotherium_ from the Miocene of Dakota, the other forms being all Eocene. They were mostly animals of small size, between that of the capybara and tapir. The skull resembled in form that of a bear; the molar teeth were of Ungulate type, and the incisors like those of a Rodent; but the skeleton was more that of the Ursidæ, the feet being plantigrade. Professor Cope has since described three new genera from the Eocene of New Mexico, _Ectoganus_, _Calamodon_, and _Esthonyx_, comprising {140}seven species allied to _Tillotherium_ and _Anchippodus_, and having also relations, as Professor Cope believes, with the South American Toxodontidæ. _Rodentia._--This order is represented in the Pliocene by a beaver, a porcupine, and an American mouse (_Hesperomys_), all extinct species of living genera, the _Hystrix_ being an Old World type; and Professor Cope has recently described _Panolax_, a new genus of hares from the Pliocene of New Mexico. The Miocene deposits have furnished an extinct genus allied to the hares--_Palæolagus_; one of the squirrel family--_Ischyromys_; a small extinct form of beaver--_Palæocastor_; and an extinct mouse--_Eumys_. The Eocene strata of Wyoming have lately furnished two extinct forms of squirrel, _Paramys_ and _Sciuravus_; and another of the Muridæ (or mouse family), _Mysops_. _Cetacea._--Numerous remains of dolphins and whales, belonging to no less than twelve genera, mostly extinct, have been found in the Miocene deposits of the Atlantic and Gulf States, from New Jersey to South Carolina and Louisiana; while seven genera of the extinct family, Zeuglodontidæ, have been found in Miocene and Eocene beds of the same districts. Some remains associated with these are doubtfully referred to the Seal family (Phocidæ) among the Carnivora. _Edentata._--Till quite recently no remains of this order have occurred in any North American deposits below the Post-Pliocene; but in 1874 Prof. Marsh described some remains allied to _Megalonyx_ and _Mylodon_, from the Pliocene beds of California and Idaho, and forming a new genus, _Morotherium_. As these remains have only occurred to the west of the Rocky Mountains, and in Pliocene deposits whose exact age is not ascertained, they hardly affect the remarkable absence of this group from the whole of the exceedingly rich Tertiary deposits in all other parts of North America. _General Relations of the extinct Tertiary Mammalia of North America and Europe._--Having now given a sketch of the extinct Mammalia which inhabited Europe and North America during the Tertiary period, we are enabled by comparing them, {141}to ascertain their relations to each other, and to see how far they elucidate the problem of the birth-place and subsequent migrations of the several families and genera. We have already pointed out the remarkable features of the Quaternary (or Post-Pliocene) fauna of North America, and now proceed to discuss that of the various Tertiary periods, which is closely connected with the extinct fauna of Europe. The Tertiary Mammalia of North America at present described belong to from eighty to one hundred genera, while those of Europe are nearly double that number; yet only eighteen genera are common to the two faunas, and of these eight are living and belong chiefly to the Pliocene period. Taking first, the genera which in America do not go back beyond the Pliocene period (ten in number), we find that eight of them in Europe go back to the Upper Miocene. These are _Felis_, _Pseudælurus_, _Hipparion_, _Cervus_, _Mastodon_, _Elephas_ (in India), _Castor_ and _Hystrix_; while another, _Canis_, goes back to the Upper Eocene and the tenth, _Equus_, confined to the newer Pliocene or perhaps to the Post-Pliocene in America, extends back to the older Pliocene in Europe. Of the seven European genera which are confined to the Miocene period in America, three, _Hyænodon_, _Anchitherium_, and _Lophiodon_ go back to the Eocene in Europe; three others, _Machairodus_, _Rhinoceros_, and _Aceratherium_, are also of Miocene age in Europe; _Amphicyon_ goes back to the Lower Miocene of Europe. _Lophiotherium_ belongs to the Eocene of both countries. If we turn now to families instead of genera, we find that the same general rule prevails. Mustelidæ (weasels), Ursidæ (bears), true Equidæ (horses), and Bovidæ (oxen &c.), go no further back in America than the Pliocene, while they all go back to the Miocene in Europe. Suidæ (swine) and Anoplotheridæ (extinct) are found in the American Miocene and in the European Eocene. Anchitheridæ (extinct) reach the Upper Eocene in America, while in Europe they range through Upper, Middle, and Lower Eocene. Cervidæ (deer) alone are Miocene in both countries. There remain two families in which America has the preeminence. Camelidæ (camels) were wonderfully developed in {142}the American Pliocene and Miocene periods, abounding in genera and species; whereas in Europe the group only exists in the Post-Pliocene or Lower Pliocene, with one Upper Miocene species of _Camelus_ in N. India. The Anthracotheridæ (extinct), found only in the Upper Miocene of France and India, reach even the Lower Eocene in America. These facts may be due, in part, to a want of strict co-ordination between the Tertiary deposits of Europe and North America,--in part to the imperfection of the record in the latter country. Yet it does not seem probable that they are altogether due South America and well marked differences to imperfect knowledge; yet we find such important families as the Civets, Hyænas, Giraffes, and Hippopotami absent from America, with the Weasels, and Antelopes almost so; while America possesses almost all the Camelidæ, two peculiar orders, Dinocerata and Tillodontia, and four remarkably peculiar families, Limnotheridæ, Lemuravidæ, Oreodontidæ and Brontotheridæ. If then the facts at present known represent approximately the real time-relations of the groups in question on the two continents, they render it probable that weasels, bears, true horses, swine, oxen, sheep and antelopes, originated on the Old World continent, and were transmitted to America during some part of the Miocene period; while camels originated in the New World, and somewhere about the same time passed over to Europe. Of the extinct families common to the two hemispheres, the Anthracotheridæ alone seem to have had an American origin. Of the genera common to the two countries, almost all seem to have had a European origin, the only genera of equal date being the two rhinoceroses and three Anchitheridæ; but if the Brontotheridæ are allied to the Rhinocerotidæ, these latter may have originated in America, although now an exclusively Old World type. These conclusions are not improbable when we consider the much greater size of the Old World continents, extending far into the tropics and probably {143}always more or less united to the tropical areas; while the evidence of the extinct mammalia themselves shows, that South America has been for the most part isolated from the northern continent, and did not take part in the development of its characteristic Tertiary fauna. Before speculating further on this subject, it will be well to lay before our readers a summary of South American palæontology, after which we shall be in a better position to draw correct inferences from the whole body of the evidence. SOUTH AMERICA. Unfortunately, our knowledge of the interesting fossil fauna of this continent, is almost wholly confined to the Post-Pliocene and Pliocene periods. A few remains have been discovered in deposits believed to be of Eocene age, but nothing whatever representing the vast intervening period, so rich in peculiar forms of animal life both in North America and Europe. _Fauna of the Brazilian caves._--What we know of the Post-Pliocene period is chiefly due to the long-continued researches of Dr. Lund in the caves of Central Brazil, mostly situated in a district near the head waters of the San Francisco river in the Province of Minas Geraes. The caves are formed in limestone rocks, and are so numerous that Dr. Lund visited thousands, but only sixty contained bones in any quantity. These caves have a floor of reddish earth, often crowded with bones. In one experiment, half a cubic foot of this earth contained jaws of 400 opossums, 2,000 mice, besides remains of bats, porcupines and small birds. In another trial, the whole of the earth in a cavern was carried out for examination, amounting to 6,552 firkins; and, from a calculation made by measured samples, it was estimated to contain nearly seven millions of jaw-bones of cavies, opossums, porcupines, and mice, besides small birds, lizards, and frogs. This immense accumulation is believed to have been formed from the bodies of animals brought into the cavern by owls; and, as these are unsocial birds, the quantity found implies an {144}immense lapse of time, probably some thousands of years. More than 100 species of Mammalia, in all, were obtained in these caves. Some were living species or closely allied to such; but the majority were extinct, and a considerable number, about one-fourth, belonged to extinct genera, or genera not now inhabiting South America. Stone implements and human remains were found in several of the caves with extinct animals. The following enumeration of these remains is from the corrected list of M. Gervais. _Primates._--Extinct species of _Cebus_, _Callithrix_, and _Jacchus_--South American genera of monkeys; with an extinct genus, _Protopithecus_--an animal of large size but belonging to the American family Cebidæ. _Chiroptera._--Species belonging to the South American Phyllostomidæ, and to two South American genera of other families. _Carnivora._--Five species of _Felis_, some allied to living animals, others extinct; a species of the widespread extinct genus _Machairodus_; and a small species referred to _Cynælurus_, the genus containing the hunting leopard now found only in Africa and India. Canidæ are represented by _Canis_ and _Icticyon_ (a living Brazilian species of the latter genus), and the extinct genus _Speothos_. Mustelidæ are represented by extinct species of the South American genera _Mephitis_ and _Galictis_. Procyonidæ, by a species of _Nasua_. Ursidæ, by _Arctotherium_, a genus closely resembling, if not identical with, that containing the "spectacled bear" of Chili. _Ungulata._--_Equus_, _Tapirus_, _Dicotyles_, _Auchenia_, _Cervus_, _Leptotherium_, and _Antilope_, are the cave-genera of this order. _Equus_ and _Antelope_ are particularly interesting, as representing groups forming no part of existing South American zoology; while the presence also of _Leptotherium_, an extinct genus of antelopes, shows that the group was fairly represented in South America at this comparatively recent period. _Proboscidea._--A species of _Mastodon_, found also in the Pliocene of La Plata, represents this order. _Rodentia._--These abound. _Dasyprocta_, _Cælogenys_, _Cavia_, _Kerodon_, all living genera of Caviidæ, are represented by {145}extinct species. _Cercolabes_, the 'tree porcupine' (Cercolabidæ) has two species, one as large as a peccary; _Myopotamus_, _Loncheres_, _Carterodon_, are existing genera of spiny rats (Echimyidæ); and there are two extinct genera of the same family, _Lonchophorus_ and _Phyllomys_. _Lagostomus_ (Chinchillidæ), the viscacha of the Pampas, is represented by an extinct species. There is also an extinct species of _Lepus_; several species of _Hesperomys_ and _Oxymycterus_; and a large _Arvicola_, a genus not living in South America. _Edentata._--These, which constitute the great feature of the existing South American fauna, were still more abundant and varied in the Cave period, and it is remarkable that most of them are extinct _genera_. The armadillos are alone represented by living forms, _Dasypus_, and _Xenurus_; _Eurydon_ and _Heterodon_, are extinct genera of the same family, as well as _Chlamydotherium_--huge armadillos the size of a tapir or rhinoceros, and _Pachytherium_, which was nearly as large. The ant-eaters are represented only by _Glossotherium_, an extinct form allied to _Myrmecophaga_ and _Manis_. The sloths were more numerous, being represented by the extinct genera _Cælodon_, _Sphenodon_ and _Ochotherium_, the last of large size. The huge terrestrial sloths--Megatheridæ, also abounded; there being species of _Megatherium_ and _Megalonyx_, as well as the allied _Scelidotherium_, supposed to have some affinity for the African _Orycteropus_. _Marsupials._--No new forms of these appear, but numerous species of _Didelphys_, all closely allied to opossums still living in South America. The preceding sketch of the wonderful cave fauna of Central Brazil, is sufficient to show that it represents, in the main, a period of great antiquity. Not only are almost the whole of the species extinct, but there are twenty extinct genera, and three others not now inhabitants of South America. The fact that so few remains of the living animals of the country are found in these caves, indicates that some change of physical conditions has occurred since they were the receptacles of so many of the larger animals; and the presence of many extinct genera of {146}large size, especially among the Edentata and American families of Rodents, are additional proofs of a very high antiquity. Yet many of these cave animals are closely allied to those which are found in North America in the Post-Pliocene deposits only, so that we have no reason to suppose the cave-fauna to be of much earlier date. But the great amount of organic change it implies, must give us an enlarged idea of the vast periods of time, as measured by years, which are included in this, the most recent of all geological epochs. _Pliocene Period of Temperate South America._--We have now to consider the numerous remains of extinct animals found in various deposits in the Pampas, and in Patagonia, and a few in Bolivia. The age of these is uncertain; but as they are very similar to the cave-fauna, though containing a somewhat larger proportion of extinct genera and some very remarkable new forms, they cannot be _very_ much older, and are perhaps best referred at present to the newer portion of the Pliocene formation. _Carnivora._--The genus _Machairodus_ or sabre-toothed tigers, represents the Felidæ. There are several species of wolves (_Canis_); a weasel (_Mustela_); two bears of the Brazilian cave-genus _Arctotherium_; and the extinct European genus _Hyænarctos_. _Ungulata._--There are two species of _Equus_, found in the Pampas, Chili, and Bolivia; two of _Macrauchenia_, an extraordinary extinct group allied to the tapir and _Palæotherium_, but with the long neck, and general size of a camel. A second species found on the highlands of Bolivia is much smaller. A more recent discovery, in Patagonia, is the almost perfect series of teeth of a large animal named _Homalodontotherium_; and which is believed by Professor Flower, who has described it, to have been allied to _Rhinoceros_, and still more to the Miocene _Hyracodon_ from North America; and also to present some resemblances to _Macrauchenia_, and though much more remotely, to the curious genus _Nesodon_ mentioned further on. The Artiodactyla, or even-toed Ungulates, are represented by a species of _Dicotyles_, or peccary, found in the deposits of the {147}Pampas; by _Auchenia_, or llama, of which three extinct species inhabited Bolivia, in which country two allied but extinct genera, _Palæolama_ and _Camelotherium_, have also been found. Three species of deer (_Cervus_), from the Pampas deposits, complete the list of Pliocene Ungulates. _Proboscidea._--The cave species of _Mastodon_ is found also in the Pampas deposits, and another in the Andes of Chili and Bolivia. _Rodents._--These are not so numerous as in the caves. There are species of the existing genera, _Kerodon_ and _Cavia_ (Caviidæ); _Lagostomus_ (Chinchillidæ); _Ctenomys_ (Octodontidæ); _Lepus_ (hare); _Hesperomys_ and _Oxymycterus_ (Muridæ); _Arvicola_, a genus not living in South America; and an extinct genus, _Cardiodus_. There is also a remarkable extinct form, _Typotherium_, larger than the capybara, and having affinities to Edentates and Ungulates. Three species have been found in the Pampas deposits. _Edentata._--These are as abundant and remarkable as in the cave deposits. _Scelidotherium_, _Megatherium_, _Megalonyx_, _Glossotherium_ and _Dasypus_, have already been noticed as from the Brazilian caves. We have here, in addition, the huge _Mylodon_ allied to the _Megatherium_, and the allied genera--_Gnathopsis_ and _Lestodon_. We then come to the huge extinct armadillos, _Glyptodon_ and _Schistopleurum_, the former consisting of numerous species, some of which were as large as an elephant. Another genus, _Eutatus_, is allied to the living three-banded armadillos; and a species of the existing genus _Euphractus_ has been found in Bolivia. _Toxodontidæ._--There remain a number of huge animals rivalling the Megatherium in size, and forming the genera _Toxodon_ and _Nesodon_, but whose position is doubtful. Several species have been found in the deposits of the Pampas and Patagonia. They are allied at once to Ungulates, Rodents, Edentates, and the aquatic Sirenia, in so puzzling a manner that it is impossible to determine to what order they belong, or whether they require a new order to be formed for their reception. Some are believed to date back to the Miocene period, and they indicate what strange forms may still be discovered, should any {148}productive deposits be found in South America of middle Tertiary age. _Pliocene Mammalia of the Antilles._--These may be noticed here, as they are of special interest, proving the connection of the larger West Indian Islands with the Continent some time in the later Tertiary period. They consist of remains of two large animals belonging to the South American Chinchillidæ, found in cave deposits in the island of Anguilla, and forming two new genera, _Amblyrhiza_ and _Loxomylus_; and remain allied to _Megalonyx_ from Cuba, which have been named _Megalocnus_ and _Myomorphus_. _Eocene fauna of South America._--The few remains yet discovered in the Tertiary deposits of the Pampas which are believed to be of Eocene age, are exceedingly interesting, because they show us another change in the scenery of the great drama of life; there being apparently a considerable resemblance, at this epoch, between South America and Europe. They consist of a large extinct feline animal, _Eutemnodus_; of _Palæotherium_ and _Anoplotherium_, the well-known extinct Ungulates of the European Tertiaries, and which have never been found in North America; and of three genera of Rodents,--_Theridromys_, allied to _Echimys_, and found also in the Eocene and Miocene of France; _Megamys_, allied to the living _Capromys_ of the Antilles, and also to _Palæomys_, an extinct form of the French Miocene; and a very large animal referred to _Arvicola_, a genus found also in the Pliocene deposits of South America, and abundant in the northern hemisphere. No Edentates have been found. The resemblances of this fauna to that of Europe rather than to any part of America, are so strong, that they can hardly be accidental. We greatly want, however, more information on this point, as well as some corresponding evidences as to the condition of West and South Africa about the same epoch, before we can venture to speculate on their bearing as regards the early migrations of organic forms. _General Remarks on the Extinct Mammalian Fauna of the Old {149}and New Worlds._--Leaving the more special applications of palæontological evidence to be made after discussing the relations of the existing fauna of the several regions, we propose here to indicate briefly, some of the more general deductions from the evidence which has now been laid before our readers. The first, and perhaps the most startling fact brought out by our systematic review, is the very recent and almost universal change that has taken place in the character of the fauna, over all the areas we have been considering; a change which seems to be altogether unprecedented in the past history of the same countries as revealed by the geological record. In Europe, in North America, and in South America, we have evidence that a very similar change occurred about the same time. In all three we find, in the most recent deposits--cave-earths, peat-bogs, and gravels--the remains of a whole series of large animals, which have since become wholly extinct or only survive in far-distant lands. In Europe, the great Irish elk, the _Machairodus_ and cave-lion, the rhinoceros, hippopotamus, and elephant;--in North America, equally large felines, horses and tapirs larger than any now living, a llama as large as a camel, great mastodons and elephants, and abundance of huge megatheroid animals of almost equal size;--in South America these same megatheroids in greater variety, numerous huge armadillos, a mastodon, large horses and tapirs, large porcupines, two forms of antelope, numerous bears and felines, including a _Machairodus_, and a large monkey,--have all become extinct since the deposition of the most recent of the fossil-bearing strata. This is certainly not a great while ago, geologically; and it is _almost_ certain that this great organic revolution, implying physical changes of such vast proportions that they must have been due to causes of adequate intensity and proportionate range, has taken place since man lived on the earth. This is proved to have been the case in Europe, and is supported by much evidence both as regards North and South America. It is clear that so complete and sudden a change in the higher forms of life, does not represent the normal state of things. Species and genera have not, at all times, become so rapidly extinct. The time occupied by the "Recent period," that is the {150}time _since_ these changes took place is, geologically, minute. The time of the whole of the Post-Pliocene period, as measured by the amount of physical and _general_ organic change known to have taken place, is exceedingly small when compared with the duration of the Pliocene period, and still smaller, probably, as compared with the Miocene. Yet during these two periods we meet with no such break in the continuity of the forms of life, no such radical change in the _character_ of the fauna (though the number of specific and generic changes may be as great) as we find in passing from the Post-Pliocene to recent times. For example, in Central Europe numerous hyænas, rhinoceroses, and antelopes, with the great _Machairodus_, continued from Miocene all through Pliocene into Post-Pliocene times; while hippopotami and elephants continued to live through a good part of the Pliocene and Post-Pliocene periods,--and then all suddenly became extinct or left the country. In North America there has been more movement of the fauna in all the periods; but we have similar great felines, horses, mastodons, and elephants, in the Pliocene and Post-Pliocene periods, while _Rhinoceros_ is common to the Miocene and Pliocene, and camels range continuously from Miocene, through Pliocene, to Post-Pliocene times;--when all alike became extinct. Even in South America the evidence is, as far as it goes, all the same way. We find _Machairodus_, _Equus_, _Mastodon_, _Megatherium_, _Scelidotherium_, _Megalonyx_, and numerous gigantic armadillos, alike in the caves and in the stratified tertiary deposits of the Pampas;--yet all have since passed away. It is clear, therefore, that we are now in an altogether exceptional period of the earth's history. We live in a zoologically impoverished world, from which all the hugest, and fiercest, and strangest forms have recently disappeared; and it is, no doubt, a much better world for us now they have gone. Yet it is surely a marvellous fact, and one that has hardly been sufficiently dwelt upon, this sudden dying out of so many large mammalia, not in one place only but over half the land surface of the globe. We cannot but believe that there must have been some physical cause for this great change; and it must have been a cause capable of acting almost simultaneously over large {151}portions of the earth's surface, and one which, as far as the Tertiary period at least is concerned, was of an exceptional character. Such a cause exists in the great and recent physical change known as "the Glacial epoch." We have proof in both Europe and North America, that just about the time these large animals were disappearing, all the northern parts of these continents were wrapped in a mantle of ice; and we have every reason to believe that the presence of this large quantity of ice (known to have been thousands of feet if not some miles in thickness) must have acted in various ways to have produced alterations of level of the ocean as well as vast local floods, which would have combined with the excessive cold to destroy animal life. There is great difference of opinion among geologists and physicists as to the extent, nature, and duration of the Glacial epoch. Some believe it to have prevailed alternately in the northern and southern hemispheres; others that it was simultaneous in both. Some think there was a succession of cold periods, each lasting many thousands of years, but with intercalated warm periods of equal duration; others deny that there is any evidence of such changes, and maintain that the Glacial epoch was one continuous period of arctic conditions in the temperate zones, with some fluctuations perhaps but with no regular alternations of warm periods. Some believe in a huge ice-cap covering the whole northern hemisphere from the pole to near 50° north latitude in the eastern, and 40° in the western hemisphere; while others impute the observed effects either to glaciers from local centres, or to floating icebergs of vast size passing over the surface during a period of submersion. Without venturing to decide which of these various theories will be ultimately proved to be correct, we may state, that there is an increasing belief among geologists in the long duration of this ice-period, and the vast extent and great thickness attained by the ice-sheet. One of the most recent, and not the least able, of the writers on this question (Mr. Belt) shows strong reasons for adopting the view that the ice-period was simultaneous in both hemispheres; and he calculates that the vast amount of water abstracted from the ocean and locked up {152}in mountains of ice around the two poles, would lower the general level of the ocean about 2,000 feet. This would be equivalent to a general elevation of the land to the same amount, and would thus tend to intensify the cold; and this elevation may enable us to understand the recent discoveries of signs of glacial action at moderate elevations in Central America and Brazil, far within the tropics. At the same time, the weight of ice piled up in the north would cause the land surface to sink there, perhaps unequally, according to the varying nature of the interior crust of the earth; and since the weight has been removed land would rise again, still somewhat irregularly; and thus the phenomena of raised beds of arctic shells in temperate latitudes, are explained. Now, it is evident, that the phenomena we have been considering--of the recent changes of the mammalian fauna in Europe, North America, South Temperate America, and the highlands of Brazil--are such as might be explained by the most extreme views as to the extent and vastness of the ice-sheet, and especially as to its simultaneous occurrence in the northern and southern hemispheres; and where two such completely independent sets of facts are found to combine harmoniously, and supplement each other on a particular hypothesis, the evidence in favour of that hypothesis is greatly strengthened. An objection that will occur to zoologists, may here be noticed. If the Glacial epoch extended over so much of the temperate and even parts of the tropical zone, and led to the extinction of so many forms of life even within the tropics, how is it that so much of the purely tropical fauna of South America has maintained itself, and that there are still such a vast number of forms, both of mammalia, birds, reptiles, and insects, that seem organized for an exclusive existence in tropical forests? Now Mr. Belt's theory, of the subsidence of the ocean to the extent of about 2,000 feet, supplies an answer to this objection; for we should thus have a tract of lowland of an average width of some hundreds of miles, added to the whole east coast of Central and South America. This tract would, no doubt, become covered with forests as it was slowly formed, would enjoy a perfectly {153}tropical climate, and would thus afford an ample area for the continued existence and development of the typical South American fauna; even had glaciers descended in places so low as what is now the level of the sea, which, however, there is no reason to believe they ever did. It is probable too, that this low tract, which all round the Gulf of Mexico would be of considerable width, offered that passage for intermigration between North and South America, which led to the sudden appearance in the former country in Post-Pliocene times, of the huge Megatheroids from the latter; a migration which took place in opposite directions as we shall presently show. _The birth-place and migrations of some mammalian families and genera._--We have now to consider a few of those cases in which the evidence already at our command, is sufficiently definite and complete, to enable us to pronounce with some confidence as to the last movements of several important groups of mammalia. _Primates._--The occurrence in North America of numerous forms of Lemuroidea, forming two extinct families, which are believed by American palæontologists to present generalized features of both Lemuridæ and Hapalidæ, while in Europe only Lemurine forms allied to those of Africa have occurred in deposits of the same age (Eocene), renders it possible that the Primates may have originated in America, and sent one branch to South America to form the Hapalidæ and Cebidæ, and another to the Old World, giving rise to the lemurs and true apes. But the fact that apes of a high degree of organization occur in the European Miocene, while in the Eocene, a monkey believed to have relations to the Lemuroids and Cebidæ has also been discovered, make it more probable that the ancestral forms of this order originated in the Old World at a still earlier period. The absence of any early tertiary remains from the tropical parts of the two hemispheres, renders it impossible to arrive at any definite conclusions as to the origin of groups which were, no doubt, always best developed in tropical regions. _Carnivora._--This is a very ancient and wide-spread group, the families and genera of which had an extensive range in very {154}early times. The true bears (_Ursus_) are almost the only important genus that seems to have recently migrated. In Europe it dates back to the Older Pliocene, while in North America it is Post-Pliocene only. Bears, therefore, seem to have passed into America from the Palæarctic region in the latter part of the Pliocene period. They probably came in on the north-west, and passed down the Andes into South America, where one isolated species still exists. _Ungulata._--Horses are very interesting. In Europe they date back under various forms to the Miocene period, and true _Equus_ to the Older Pliocene. In North America they are chiefly Pliocene, true _Equus_ being Post-Pliocene, with perhaps one or two species Newer Pliocene; but numerous ancestral forms date back to the Miocene and Eocene, giving a more perfect "pedigree of the horse" than the European forms, and going back to a more primitive type--_Orohippus_. In South America, _Equus_ is the only genus, and is Post-Pliocene or at most Newer Pliocene. While, therefore, the ancient progenitors of the Equidæ were common to North America and Europe, in Miocene and even Eocene times, true horses appear to have arisen in the Palæarctic region, to have passed into North America in the latter part of the Pliocene period, and thence to have spread over all suitable districts in South America. They were not, however, able to maintain themselves permanently in their new territory, and all became extinct; while in their birth-place, the Old World, they continue to exist under several varied forms. True tapirs are an Old World group. They go back to the Lower Miocene in Europe, while in both North and South America they are exclusively Post-Pliocene. They occur in France down to the Newer Pliocene, and must, about that time, have entered America. The land connection by which this and so many other animals passed between the Old and New Worlds in late Tertiary times, was almost certainly in the North Pacific, south of Behring's Straits, where, as will be seen by our general map, there is a large expanse of shallow water, which a moderate elevation would convert into dry land, in a sufficiently temperate latitude. {155}The peccary (_Dicotyles_), now a characteristic South American genus, is a recent immigrant from North America, where it appears to have been developed from ancestral forms of swine dating back to the Miocene period. Antelopes are an Old World type, but a few of them appear to have entered North, and reached South America in late Pliocene times. Camels, strange to say, are a special North American type, since they abounded in that continent under various ancient forms in the Miocene period. Towards the end of that period they appear to have entered eastern Asia, and developed into the Siberian _Merycotherium_ and the North Indian _Camelus_, while in the Pliocene age the ancestral llamas entered South America. _Cervidæ_ are a wide-spread northern type in their generalized form, but true deer (_Cervus_) are Palæarctic. They abounded in Europe in Miocene times, but only appear in North and South America in the later Pliocene and Post-Pliocene periods. True oxen (_Bovinæ_) seem to be an Oriental type (Miocene), while they appear in Europe only late in the Pliocene period, and in America are confined to the Post-Pliocene. Elephants (_Elephantidæ_) are an Old World type, abounding in the Miocene period in Europe and India, and first appearing in America in Post-Pliocene or later Pliocene times. Ancestral forms, doubtfully Proboscidean (_Dinocerata_), existed in North America in the Eocene period, but these became extinct without leaving any direct descendants, unless the _Brontotheridæ_ and rhinoceroses may be so considered. Marsupials are almost certainly a recent introduction into South and North America from Asia. They existed in Europe in Eocene and Miocene times, and presumably over a considerable part of the Old World; but no trace of them appears in North or South America before the Post-Pliocene period. _Edentata._--These offer a most curious and difficult problem. In South America they abound, and were so much more numerous and varied in the Post-Pliocene and Pliocene, that we may be sure they lived also in the preceding Miocene period. A few living Edentates are scattered over Africa and Asia, and {156}they flourished in Europe during the Miocene age--animals as large (in some species) as a rhinoceros, and most allied to living African forms. In North America no trace of Edentata has been found earlier than the Post-Pliocene period, or perhaps the Newer Pliocene on the west coast. Neither is there any trace of them in South America in the Eocene formations; but this may well be owing to our very imperfect knowledge of the forms of that epoch. Their absence from North America is, however, probably real; and we have to account for their presence in the Old World and in South America. Their antiquity is no doubt very great, and the point of divergence of the Old World and South American groups, may take us back to early Eocene, or even to Pre-Eocene times. The distribution of land and sea may then have been very different from what it is now; and to those who would create a continent to account for the migrations of a beetle, nothing would seem more probable than that a South Atlantic continent, then united parts of what are now Africa and South America. There is, however, so much evidence for the general permanence of what are now the great continents and deep oceans, that Professor Huxley's supposition of a considerable extension of land round the borders of the North Pacific Ocean in Mesozoic times, best indicates the probable area in which the Edentate type originated, and thence spread over much of the Old World and South America. But while in the latter country it flourished and increased with little check, in the other great continents it was soon overcome by the competition of higher forms, only leaving a few small-sized representatives in Africa and Asia. {157}CHAPTER VIII. VARIOUS EXTINCT ANIMALS;--AND ON THE ANTIQUITY OF THE GENERA OF INSECTS AND LAND MOLLUSCA. EXTINCT MAMMALIA OF AUSTRALIA. These have all been obtained from caves and late Tertiary or Post-Tertiary deposits, and consist of a large number of extinct forms, some of gigantic size, but all marsupials and allied to the existing fauna. There are numerous forms of kangaroos, some larger than any living species; and among these are two genera, _Protemnodon_ and _Sthenurus_, which Professor Garrod has lately shown to have been allied, not to any Australian forms, but to the _Dendrolagi_ or tree-kangaroos of New Guinea. We have also remains of _Thylacinus_ and _Dasyurus_, which now only exist in Tasmania; and extinct species of _Hypsiprymnus_ and _Phascolomys_, the latter as large as a tapir. Among the more remarkable extinct genera are _Diprotodon_, a huge thick-limbed animal allied to the kangaroos, but nearly as large as an elephant; _Nototherium_, having characters of _Macropus_ and _Phascolarctos_ combined, and as large as a rhinoceros; and _Thylacoleo_, a phalanger-like marsupial nearly as large as a lion, and supposed by Professor Owen to have been of carnivorous habits, though this opinion is not held by other naturalists. Here then we find the same phenomena as in the other countries we have already discussed,--the very recent disappearance of a large number of peculiar forms, many of them far surpassing in size any that continue to exist. It hardly seems probable that in this case their disappearance can have been due to the direct effects of the Glacial epoch, since no very extensive {158}glaciation could have occurred in a country like Australia; but if the ocean sank 2,000 feet, the great eastern mountain range might have given rise to local glaciers. It is, however, almost certain that during late Tertiary times Australia must have been much more extensive than it is now. This is necessary to allow of the development of its peculiar and extensive fauna, especially as we see that that fauna comprised animals rivalling in bulk those of the great continents. It is further indicated by the relations with New Guinea, already alluded to, and by the general character of the various faunas which compose the Australian region, details of which will be found in the succeeding part of this work. The lowering of the ocean during the Glacial period would be favourable to the still further development of the fauna of such a country; and it is to the unfavourable conditions produced by its subsequent rising--equivalent to a depression of the land to the amount of two thousand feet--that we must impute the extinction of so many remarkable groups of animals. It is not improbable, that the disappearance of the ice and the consequent (apparent) subsidence of the land, might have been rapid as compared with the rate at which large animals can become modified to meet new conditions. Extensive tracts of fertile land might have been submerged, and the consequent crowding of large numbers of species and individuals on limited areas would have led to a struggle for existence in which the less adapted and less easily modifiable, not the physically weaker, would succumb. There is, however, another cause for the extinction of large rather than small animals whenever an important change of conditions occurs, which has been suggested to me by a correspondent,[4] but which has not, I believe, been adduced by Mr. Darwin or by any other writer on the subject. It is dependent on the fact, that large animals as compared with small ones are almost invariably slow breeders, and as they also necessarily exist in much smaller numbers in a given area, they offer far less materials for favourable variations than do smaller animals. In such an extreme case as that of the rabbit and elephant, the {159}young born each year in the world are probably as some millions to one; and it is very easily conceivable that in a thousand years the former might, under pressure of rapidly changing conditions, become modified into a distinct species, while the latter, not offering enough favourable variations to effect a suitable adaptation, would become extinct. We must also remember the extreme specialization of many of the large animals that have become extinct--a specialization which would necessarily render modification in any new direction difficult, since the inherited tendency of variation would probably be to increase the specialization in the same directions which had heretofore been beneficial. If to these two causes we add the difficulty of obtaining sufficient food for such large animals, and perhaps the injurious effects of changes of climate, we shall not find it difficult to understand how such a vast physical revolution as the Glacial epoch, with its attendant phenomena of elevations and subsidences, icy winds, and sudden floods by the bursting of lake barriers, might have led to the total extinction of a vast number of the most bulky forms of mammalia, while the less bulky were able to survive, either by greater hardiness of constitution or by becoming more or less modified. The result is apparent in the comparatively small or moderate size of the species constituting the temperate fauna, in all parts of the globe. It is much to be regretted that no mammalian remains of earlier date have been found in Australia, as we should then see if it is really the case that marsupials have always formed its highest type of mammalian life. At present its fossil fauna is chiefly interesting to the zoologist, but throws little light on the past relations of this isolated country with other parts of the globe. MAMMALIAN REMAINS IN THE SECONDARY FORMATIONS. In the oldest Tertiary beds of Europe and North America, we have (even with our present imperfect record) a rich and varied mammalian fauna. As compared with our living or recent highly specialized forms, it may be said to consist of generalised types; but as compared with any primeval mammalian type, it must be pronounced highly specialised. Not only are such diversified {160}groups as Carnivora, Perrissodactyle and Artiodactyle Ungulates, Primates, Chiroptera, Rodents, and Marsupials already well marked, but in many of these there is a differentiation into numerous families and genera of diverse character. It is impossible therefore to doubt, that many peculiar forms of mammalia must have lived long anterior to the Eocene period; but there is unfortunately a great gap in the record between the Eocene and Cretaceous beds, and these latter being for the most part marine continue the gap as regards mammals over an enormous lapse of time. Yet far beyond both these chasms in the Upper Oolitic strata, remains of small mammalia have been found; again, in the Stonesfield slate, a member of the Lower Oolite, other forms appear. Then comes the marine Lias formation with another huge gap; but beyond this again in the Upper Trias, the oldest of the secondary formations, mammalian teeth have been discovered in both England and Germany, and these are, as nearly as can be ascertained, of the same age as the _Dromatherium_ already noticed, from North America. They have been named _Microlestes_, and show some resemblance to those of the West Australian _Myrmecobius_. In the Oolitic strata numerous small jawbones have been found, which have served to characterise eight genera, all of which are believed to have been Marsupials, and in some of them a resemblance can be traced to some of the smaller living Australian species. These, however, are mere indications of the number of mammalia that must have lived in the secondary period, so long thought to be exclusively "the age of reptiles;" and the fact that the few yet found are at all comparable with such specialised forms as still exist, must convince us, that we shall have to seek far beyond even the earliest of these remains, for the first appearance of the mammalian type of vertebrata. EXTINCT BIRDS. Compared with those of mammalia, the remains of birds are exceedingly scarce in Europe and America; and from the wandering habits of so many of this class, they are of much less value {161}as indications of past changes in physical geography. A large proportion of the remains belong to aquatic or wading types, and as these have now often a world-wide range, the occurrence of extinct forms can have little bearing on our present inquiry. There are, however, a few interesting cases of extinct land-birds belonging to groups now quite strangers to the country in which they are found; and others scarcely less interesting, in which groups now peculiar to certain areas are shown to have been preceded by allied species or genera of gigantic size. _Palæarctic Region and N. India._--In the caves and other Post-Pliocene deposits of these countries, the remains of birds almost all belong to genera now inhabiting the same districts. Almost the only exceptions are, the great auk and the capercailzie, already mentioned as being found in the Danish mounds; the latter bird, with _Tetrao albus_, in Italian caverns; and a species of pheasant (_Phasianus_) said to have occurred in the Post-Pliocene of France, considerably west of the existing range of the genus in a wild state. In the preceding Pliocene deposits, but few remains have been found, and all of existing genera but one, a gallinaceous bird (_Gallus bravardi_) allied to the domestic fowl and peacock. The Miocene beds of France and Central Europe have produced many more remains of birds, but these, too, are mostly of existing European genera, though there are some notable exceptions. Along with forms undistinguishable from crows (_Corvus_), shrikes (_Lanius_), wagtails (_Motacilla_), and woodpeckers (_Picus_), are found remains allied to the Oriental edible-nest swift (_Collocalia_) and _Trogon_; a parrot resembling the African genus _Psittacus_; an extinct form _Necrornis_, perhaps allied to the plantain-eaters (_Musophaga_); _Homalophus_, doubtfully allied to woodpeckers, and _Limnatornis_ to the hoopoes. The gallinaceous birds are represented by three species of pheasants, some very close to the domesticated species; _Palæoperdix_ allied to the partridges; and _Palæortyx_, small birds allied to the American genus _Ortyx_, but with larger wings. There are also species of _Pterocles_ allied to living birds, and a small pigeon. There are numerous living genera of Accipitres; such as eagle (_Aquila_), {162}kite (_Milvus_), eagle-owl (_Bubo_), and screech-owl (_Strix_); with the African secretary-bird (_Serpentarius_), and some extinct forms, as _Palæocercus_, _Palæohierix_ and _Palæetus_. Aquatic and wading birds were abundant, including numerous rails, bustards, herons, sandpipers, gulls, divers, and pelicans. There were also many ducks, some allied to the genus _Dendrocygna_; the Oriental genus of storks, _Leptoptilus_; _Ibidipodia_, a remarkable form allied to _Ibis_ and _Ciconia_; _Elornis_, near _Limosa_; _Pelagornis_, a large bird allied to gannets and pelicans; _Hydrornis_, allied to the ducks and petrels; _Dolichopterus_, allied to plovers. Perhaps the most interesting of these extinct birds are, however, the flamingoes, represented by forms hardly distinguishable from living species, and by one extinct genus _Palælodus_, which had very long toes, and probably walked on aquatic plants like the tropical jacanas. The Miocene beds of North India have furnished few birds; the only one of geographical interest being an extinct species of ostrich, not very different from that now inhabiting Arabia. On the whole, the birds of Europe at this period were very like those now living, with the addition of a few tropical forms. These latter were, however, perhaps more numerous and important than they appear to be, as they belong to inland and forest-haunting types, which would not be so frequently preserved as the marsh and lake-dwelling species. Taking this into consideration, the assemblage of Miocene birds accords well with what we know of the mammalian fauna. We have the same indications of a luxuriant vegetation and subtropical climate, and the same appearance of Oriental and especially of African types. _Trogon_ is perhaps the most interesting of all the forms yet discovered, since it furnishes us with a central point whence the living trogons of Asia, Africa, and South America might have diverged. In the Eocene we find ourselves almost wholly among extinct forms of birds. The earliest known Passerine bird is here met with, in _Protornis_, somewhat similar to a lark, found in the Lower Eocene of Switzerland; while another Passerine form, _Palægithalus_, and one allied to the nuthatch (_Sitta_), have been {163}discovered in the Upper Eocene of Paris. Picariæ of equal antiquity are found. _Cryptornis_, from the Paris Eocene, and _Halcyornis_ from the Lower Eocene of the Isle of Sheppey, were both allied to kingfishers; while a form allied to _Centropus_ a genus of cuckoos, or, as Milne-Edwards thinks, to the Madagascar _Leptosomus_, has been found in the Upper Eocene of France. Several _Accipitres_ of somewhat doubtful affinities have been found in the same country; while _Lithornis_, from the Lower Eocene of the Isle of Sheppey, was a small vulturine bird supposed to be allied to the American group, _Cathartes_. Among the waders, some extinct forms of plovers have been found, and a genus (_Agnopterus_), allied to the flamingoes; while there are many swimming birds, such as pelicans, divers, and several extinct types of doubtful affinities. Most intersting of all is a portion of a cranium discovered in the Lower Eocene of Sheppey, and lately pronounced by Professor Owen to belong to a large Struthious bird, allied to the New Zealand _Dinornis_ and also perhaps to the ostrich. Another gigantic bird is the _Gastornis_, from the Lower Eocene of Paris, which was as large as an ostrich, but which is believed to have been a generalised type, allied to wading and swimming birds as well as to the Struthiones. Beyond this epoch we have no remains of birds in European strata till we come to the wonderful _Archæopteryx_ from the Upper Oolite of Bavaria; a bird of a totally new type, with a bony tail, longer than the body, each vertebra of which carried a pair of diverging feathers. _North America._--A number of bird-remains have lately been found in the rich Tertiary and Cretaceous deposits of the United States; but here, too, comparatively few are terrestrial forms. No Passerine bird has yet been found. The Picariæ are represented by _Uintornis_, an extinct form allied to woodpeckers, from the Eocene of Wyoming. Species of turkey (_Meleagris_) occur in the Post-Pliocene and as far back as the Miocene strata, showing that this interesting type is a true denizen of temperate North America. The other birds are, _Accipitres_; waders and aquatics of existing genera; and a number of extinct forms of the two latter orders--such as, _Aletornis_ an Eocene wader; {164}_Palæotringa_, allied to the sandpipers, and _Telmatobius_ to the rails, both Cretaceous; with _Graculavus_, allied to _Graculus_; _Laornis_ allied to the swans; _Hesperornis_ a gigantic diver; and _Icthyornis_ a very low form, with biconcave vertebra, such as are only found in fishes and some reptiles--also from Cretaceous deposits. _South America._--The caverns of Brazil produced thirty-four species of birds, most of them referable to Brazilian genera, and many to still existing species. The most interesting were two species of American ostrich (_Rhea_), one larger than either of the living species; a large turkey-buzzard (_Cathartes_); a new species of the very isolated South American genus _Opisthocomus_; and a _Cariama_, or allied new genus. _Madagascar and the Mascarene Islands._--We have here only evidence of birds that have become extinct in the historical period or very little earlier. First we have a group of birds incapable of flight, allied to pigeons, but forming a separate family, _Dididæ_; and which, so far as we yet know, inhabited Mauritius, Rodriguez, and probably Bourbon. _Aphanapteryx_, an extinct genus of rails, inhabited Mauritius; and another genus, (_Erythromachus_), Rodriguez. A large parrot, said by Prof. Milne Edwards to be allied to _Ara_ and _Microglossus_, also inhabited Mauritius; and another allied to _Eclectus_, the island of Rodriguez. None of these have been found in Madagascar; but a gigantic Struthious bird, _Æpyornis_, forming a peculiar family distinct both from the ostriches of Africa and the _Dinornis_ of New Zealand inhabited that island; and there is reason to believe that this may have lived less than 200 years ago. _New Zealand._--A number of extinct Struthious birds, forming two families, _Dinornithidæ_ and _Palapterygidæ_, have been found in New Zealand. Some were of gigantic size. They seem allied both to the living _Apteryx_ of New Zealand and the emu of Australia. They are quite recent, and some of them have probably lived within the last few centuries. Remains of _Dinornis_ have also been found in a Post-Pliocene deposit in Queensland, N. E. Australia[5]--a very important discovery, as it {165}gives support to the theory of a great eastward extension of Australia in Tertiary times. EXTINCT TERTIARY REPTILES. These will not occupy us long, as no very great number are known, and most of them belong to a few principal forms of comparatively little geographical interest. Tortoises are perhaps the most abundant of the Tertiary reptiles. They are numerous in the Eocene and Miocene formations both in Europe and North America. The genera _Emys_ and _Trionyx_ abound in both countries, as well as in the Miocene of India. Land tortoises occur in the Eocene of North America and in the Miocene of Europe and India, where the huge _Colossochelys_, twelve feet long, has been found. In the Pliocene deposits of Switzerland the living American genus _Chelydra_ has been met with. These facts, together with the occurrence of a living _species_ in the Miocene of India, show that this order of reptiles is of great antiquity, and that most of the genera once had a wider range than now. Crocodiles, allied to the three forms now characteristic of India, Africa, and America, have been found in the Eocene of our own country, and several species of _Crocodilus_ have occurred in beds of the same age in North America. Lizards are very ancient, many small terrestrial forms occurring in all the Tertiary deposits. A species of the genus _Chamæleo_ is recorded from the Eocene of North America, together with several extinct genera. Snakes were well developed in the Eocene period, where remains of several have been found which must have been from twelve to twenty feet long. An extinct species of true viper has occurred in the Miocene of France, and one of the Pythonidæ in the Miocene brown coal of Germany. Batrachia occur but sparingly in a fossil state in the Tertiary deposits. The most remarkable is the large Salamander (_Andreas_) from the Upper Miocene of Switzerland, which {166}is allied to the _Menopoma_ living in North America. Species of frog (_Rana_), and _Palæophryus_ an extinct genus of toads, have been found in the Miocene deposits of Germany and Switzerland. Fresh water fish are almost unknown in the Tertiary deposits of Europe, although most of the families and some genera of living marine fish are represented from the Eocene downwards. ANTIQUITY OF THE GENERA OF INSECTS. Fossil insects are far too rarely found, to aid us in our determination of difficult questions of geographical distribution; but in discussing these questions it will be important to know, whether we are to look upon the existing generic forms of insects as of great or small antiquity, compared with the higher vertebrates; and to decide this question the materials at our command are ample. The conditions requisite for the preservation of insects in a fossil state are no doubt very local and peculiar; the result being, that it is only at long intervals in the geological record that we meet with remains of insects in a recognisable condition. None appear to have been found in the Pliocene formation; but in the Upper Miocene of Oeninghen in Switzerland, associated with the wonderfully rich fossil flora, are found immense quantities of insects. Prof. Heer examined more than 5,000 specimens belonging to over 800 species, and many have been found in other localities in Switzerland; so that more than 1,300 species of Miocene insects have now been determined. Most of the orders are represented, but the beetles (Coleoptera) are far the most abundant. Almost all belong to existing genera, and the majority of these genera now inhabit Europe, only three or four being exclusively Indian, African, or American. In the Lower Miocene of Croatia there is another rich deposit of insects, somewhat more tropical in character, comprising large white-ants and dragon-flies differently marked from any {167}now inhabiting Europe. A butterfly is also well preserved, with all the markings of the wings; and it seems to be a _Junonia_, a tropical genus, though it may be a _Vanessa_, which is European, but the fossil most resembles Indian species of _Junonia_. The Eocene formations seem to have produced no insect remains; but they occur again in the Upper Cretaceous at Aix-la-Chapelle, where two butterflies have been found, _Cyllo sepulta_ and _Satyrites Reynesii_, both belonging to the Satyridæ, and the former to a genus now spread over Africa, India, and Australia. A little earlier, in the Wealden formation of our own country, numerous insects have been found, principally dragon flies (_Libellula_, _Æshna_); aquatic Hemiptera (_Velia Hydrometra_); crickets, cockroaches, and cicadas, of familiar types. Further back in the Upper Oolite of Bavaria--which produced the wonderful long-tailed bird, _Archæopteryx_--insects of all orders have been found, including a moth referred to the existing genus _Sphinx_. In the Lower Oolite of Oxfordshire many fossil beetles have been found whose affinities are shown by their names:--_Buprestidium_, _Curculionidium_, _Blapsidium_, _Melolonthidium_, and _Prionidium_; a wing of a butterfly has also been found, allied to the Brassolidæ now confined to tropical America, and named _Palæontina oolitica_. Still more remote are the insects of the Lias of Gloucestershire, yet they too can be referred to well-known family types--Carabidæ, Melolonthidæ, Telephoridæ, Elateridæ, and Curculionidæ, among beetles; Gryllidæ and Blattidæ among Orthoptera; with _Libellula_, _Agrion_, _Æshna_, _Ephemera_, and some extinct genera. When we consider that almost the only vertebrata of this period were huge Saurian reptiles like the _Icthyosaurus_, _Plesiosaurus_, and _Dinosaurus_, with the flying Pterodactyles; and that the great mass of our existing genera, and even families, of fish and reptiles had almost certainly not come into existence, we see at once that types of insect-form are, proportionately, far more ancient. At this remote epoch we find the chief family types (the _genera_ of the time of Linnæus) perfectly differentiated {168}and recognisable. It is only when we go further back still, into the Palæozoic formations, that the insect forms begin to show that generalization of type which renders it impossible to classify them in any existing groups. Yet even in the coal formation of Nova Scotia and Durham, the fossil insects are said by competent entomologists to be "allied to _Ephemera_," "near _Blatta_," "near _Phasmidæ_;" and in deposits of the same age at Saarbrück near Trèves, a well-preserved wing of a grasshopper or locust has been found, as well as a beetle referred to the Scarabeidæ. More remarkable, however, is the recent discovery in the carboniferous shales of Belgium, of the clearly-defined wing of a large moth (_Breyeria borinensis_), closely resembling some of the Saturniidæ; so that we have now all the chief orders of Insects--including those supposed to be the most highly developed and the most recent--well represented at this very remote epoch. Even the oldest insects, from the Devonian rocks of North America, can mostly be classed as Neuroptera or Myriapoda, but appear to form new families. We may consider it, therefore, as proved, that many of the larger and more important genera of insects date back to the beginning of the Tertiary period, or perhaps beyond it; but the family types are far older, and must have been differentiated very early in the Secondary period, while some of them perhaps go back to Palæozoic times. The great comparative antiquity of the _genera_ is however the important fact for us, and we shall have occasion often to refer to it, in endeavouring to ascertain the true bearing of the facts of insect distribution, as elucidating or invalidating the conclusions arrived at from a study of the distribution of the higher animals. ANTIQUITY OF THE GENERA OF LAND AND FRESH-WATER SHELLS. The remains of land and fresh-water shells are not much more frequent than those of insects. Like them, too, their forms are very stable, continuing unchanged through several geological {169}periods. In the Pliocene and Miocene formations, most of the shells are very similar to living species, and some are quite identical. In the Eocene we meet with ordinary forms of the genera _Helix_, _Clausilia_, _Pupa_, _Bulimus_, _Glandina_, _Cyclostoma_, _Megalostoma_, _Planorbis_, _Paludina_ and _Limnæa_, some resembling European species, others more like tropical forms. A British Eocene species of _Helix_ is still living in Texas; and in the South of France are found species of the Brazilian sub-genera _Megaspira_ and _Anastoma_. In the secondary formation no true land shells have been found, but fresh water shells are tolerably abundant, and almost all are still of living forms. In the Wealden (Lower Cretaceous) and Purbeck (Upper Oolite) are found _Unio_, _Melania_, _Paludina_, _Planorbis_, and _Limnæa_; while the last named genus occurs even in the Lias. The notion that land shells were really not in existence during the secondary period is, however, proved to be erroneous by the startling discovery, in the Palæozoic coal measures of Nova Scotia, of two species of Helicidæ, both of living genera--_Pupa vetusta_, and _Zonites priscus_. They have been found in the hollow trunk of a _Sigillaria_, and in great quantities in a bed full of Stigmarian rootlets. The most minute examination detects no important differences of form or of microscopic structure, between these shells and living species of the same genera! These mollusca were the contemporaries of Labyrinthodonts and strange Ganoid fishes, which formed almost the whole vertebrate fauna. This unexpected discovery renders it almost certain, that numbers of other existing genera, of which we have found no traces, lived with these two through the whole secondary period; and we are thus obliged to assume as a probability, that any particular genus has lived through a long succession of geological ages. In estimating the importance of any peculiarities or anomalies in the geographical distribution of land shells as compared with the higher vertebrates, we shall, therefore, have to keep this possible, and even probable high antiquity, constantly in mind. We have now concluded our sketch of Tertiary Palæontology as a preparation for the intelligent study of the Geographical {170}Distribution of Land Animals; and however imperfectly the task has been performed, the reader will at all events have been convinced that some such preliminary investigation is an essential and most important part of our work. So much of palæontology is at present tentative and conjectural, that in combining the information derived from numerous writers, many errors of detail must have been made. The main conclusions have, however, been drawn from as large a basis of facts as possible; and although fresh discoveries may show that our views as to the past history of some of the less important genera or families are erroneous, they can hardly invalidate our results to any important degree, either as regards the intercommunications between separate regions in the various geological epochs, or as to the centres from which some of the more important groups have been dispersed. PART III. _ZOOLOGICAL GEOGRAPHY:_ _A REVIEW OF THE CHIEF FORMS OF ANIMAL LIFE IN THE SEVERAL REGIONS AND SUB-REGIONS, WITH THE INDICATIONS THEY AFFORD OF GEOGRAPHICAL MUTATIONS._ {173}CHAPTER IX. THE ORDER OF SUCCESSION OF THE REGIONS.--COSMOPOLITAN GROUPS OF ANIMALS.--TABLES OF DISTRIBUTION. Having discussed, in our First Part, such general and preliminary matters as are necessary to a proper comprehension of our subject; and having made ourselves acquainted, in our Second Part, with the most important results of Palæontology, we now come to our more immediate subject, which we propose to treat first under its geographical aspect. Taking each of our six regions in succession, we shall point out in some detail the chief zoological features they present, as influenced by climate, vegetation, and other physical features. We shall then treat each of the sub-regions by itself, as well as such of the islands or other sub-divisions as present features of special interest; endeavouring to ascertain their true relations to each other, and the more important changes of physical geography that seem necessary to account for their present zoological condition. _Order of Succession of the Regions._--We may here explain the reason for taking the several regions in a different succession from that in which they appear in the tabular or diagrammatic headings to each family, in the Fourth, and concluding part of this work. It will have been seen, by our examination of extinct animals (and it will be made still clearer during our study of the several regions) that all the chief types of animal life appear to have originated in the great north temperate or northern continents; while the southern continents--now represented by {174}South America, Australia, and South Africa with Madagascar--have been more or less completely isolated, during long periods, both from the northern continent and from each other. These latter countries have, however, been subject to more or less immigration from the north during rare epochs of approximation to, or partial union with it. In the northern, more extensive, and probably more ancient land, the process of development has been more rapid, and has resulted in more varied and higher types; while the southern lands, for the most part, seem to have produced numerous diverging modifications of the lower grades of organization, the original types of which they derived either from the north, or from some of the ancient continents in Mesozoic or Palæozoic times. Hence those curious resemblances in the fauna of South America, Australia, and, to a less extent, Madagascar, which have led to a somewhat general belief that these distant countries must at one time or other have been united; a belief which, after a careful examination of all the facts, does not seem to the author of this work to be well founded. On the other hand, there is the most satisfactory evidence that each southern region has been more or less closely united (during the tertiary or later secondary epoch) with the great northern continents, leading to numerous resemblances and affinities in their productions. In endeavouring to present at a glance in the most convenient manner, the distribution of the families in the several regions and sub-regions, it was necessary to arrange them, so that those whose relations to each other were closest should stand side by side; the first and last being those between which the relations were least numerous and least important. Influenced by the usual opinions as to the relations between Australia and South America, the series was at first begun with the Nearctic, and terminated with the Australian and Neotropical regions; and it was not till the whole of the vertebrate families had been gone through, and their distribution carefully studied, that these last two regions were seen to be really wider apart than any others of the series. It was therefore decided to alter the arrangement, beginning with the Neotropical, and ending with the Australian {175}regions; and a careful inspection of the diagrams themselves, taken in their entirety, will, it is believed, show that this is the most natural plan, and most truly exhibits the relations of the several regions. In the portion of our work now commencing, we are not, however, by any means bound to begin at either end of this series. Each region is studied by itself, but reference will often have to be made to all the other regions; and wherever we begin, we must occasionally refer to facts which will be given further on. As, however, the great northern continents form the central mass from which the southern regions, as it were, diverge, and as the Palæarctic region is both more extensive and much better known than any other, it undoubtedly forms the most convenient starting-point for our proposed survey of the zoological history of the earth. We thus pass from the better known to the less known--from Europe to Africa and tropical Asia, and thence to Australia, completing the series of regions of the Eastern Hemisphere. Beginning again with the Neotropical region, we pass to the Nearctic, which has such striking relations with the preceding and with the Palæarctic region, that it can only be properly understood by constant reference to both. We thus keep separate the Eastern and Western hemispheres, which form, from our point of view, the most radical and most suggestive division of terrestrial faunas; and as we are able to make this also the dividing point of our two volumes, reference to the work will be thereby facilitated. _Cosmopolitan Groups._--Before proceeding to sketch the zoological features of the several Regions it will be well to notice those family groups which belong to the earth as a whole, and which are so widely and universally distributed over it that it will be unnecessary, in some cases, to do more than refer to them under the separate geographical divisions. The only absolutely cosmopolitan families of Mammalia are those which are aerial or marine; and this is one of the striking proofs that their distribution has been effected by natural causes, and that the permanence of barriers is one of the chief {176}agencies in the limitation of their range. Even among the aerial bats, however, only one family--the Vespertilionidæ--is truly cosmopolitan, the others having a more or less restricted range. Neither are the Cetacea necessarily cosmopolitan, most of the families being restricted either to warm or to cold seas; but one family, the dolphins (Delphinidæ), is truly so. This order however will not require further notice, as, being exclusively marine the groups do not enter into any of our terrestrial regions. The only other family of mammals that may be considered to be cosmopolitan, is the Muridæ (rats and mice); yet these are not entirely so, since none are known to be truly indigenous in any part of the Australian region except Australia itself. In the class of Birds, a number of families are cosmopolites, if we reckon as such all which are found in each region and sub-region; but several of these are so abundant in some parts, while they are so sparingly represented in others, that they cannot fairly be considered so. We shall confine that term therefore, to such as, there is reason to believe, inhabit every important sub-division of each region. Such are, among the Passerine birds the crows (Corvidæ), and swallows (Hirundinidæ); among the Picariæ the kingfishers (Alcedinidæ); among other Land birds the pigeons (Columbidæ), grouse and partridges (Tetraonidæ), hawks (Falconidæ), and owls (Strigidæ); among the Waders the rails (Rallidæ), snipes (Scolopacidæ), plovers (Charadriadæ), and herons (Ardeidæ); and among the Swimmers the ducks (Anatidæ), gulls (Laridæ), petrels (Procellariidæ), pelicans (Pelecanidæ), and grebes (Podicipidæ). In the class of Reptiles there are few absolutely cosmopolitan families, owing to the scarcity of members of this group in some insular sub-regions, such as New Zealand and the Pacific Islands. Those which are most nearly so are the Colubridæ among snakes, and the Scincidæ among lizards. There is no cosmopolitan family of Amphibia, the true frogs (Ranidæ) being the most widely distributed. Neither is any family of Freshwater Fishes cosmopolitan, the Siluridæ, which have the widest range, being confined {177}to warm regions, and becoming very scarce in the temperate zones. Among the Diurnal and Crepuscular Lepidoptera (butterflies and sphinges) the following families are cosmopolitan:--Satyridæ, Nymphalidæ, Lycænidæ, Pieridæ, Papilionidæ, Hesperidæ, Zygænidæ, and Sphingidæ. Of the Coleoptera almost all, except some of the small and obscure families, are cosmopolitan. Of the terrestrial Mollusca, the Helicidæ alone are true cosmopolites. _Tables of Distribution of Families and Genera._--Having been obliged to construct numerous tables of the distribution of the various groups for the purposes of the descriptive part of the work, I have thought it well to append the most important of them, in a convenient form, to the chapter on each region; as much information will thereby be given, which can only be obtained from existing works at the cost of great labour. All these tables are drawn up on a uniform plan, the same generic and family names being used in each; and all are arranged in the same systematic order, so as to be readily comparable with each other. This, although it seems a simple and natural thing to do, has involved a very great amount of labour, because hardly two authors use the same names or follow the same arrangement. Hence comparison between them is impossible, till all their work has been picked to pieces, their synonymy unravelled, their differences accounted for, and the materials recast; and this has to be done, not for two or three authors only, but for the majority of those whose works have been consulted on the zoology of any part of the globe. Except in the two higher orders--Mammalia and Birds--materials do not exist for complete tables of the genera brought down to the present time. We have given therefore, first, a complete table of all the families of Vertebrata and Diurnal Lepidoptera found in each region, showing the sub-regions in which they occur, and their range beyond the limits of the region. Families which are wholly peculiar to the region, or {178}very characteristic and almost exclusively confined to it, are in _italics_. The number prefixed to each family corresponds to that of the series of families in the Fourth Part of this work, so that if further information is required it can be readily referred to without consulting the index. Names inclosed in parentheses--( . . . ) thus--indicate families which only just enter a region from an adjacent one, to which they properly belong. The eye is thus directed to the more, and the less important families; and a considerable amount of information as to the general features of the zoology of the region, is conveyed in the easiest manner. The tables of genera of Mammalia and Birds, are arranged on a somewhat different plan. Each genus is given under its Family and Order, and they follow in the same succession in all the tables. The number of species of each genus, inhabiting the region, is given as nearly as can be ascertained; but in many cases this can only be a general approximation. The distribution of the genera within the region, is then given with some detail; and, lastly, the range of the genus beyond the region is given in general terms, the words "Oriental," "Ethiopian," &c., being used for brevity, to indicate that the genus occurs over a considerable part of such regions. Genera which are restricted to the region (or which are very characteristic of it though just transgressing its limits) are given in _italics_; while those which only just enter the region from another to which they really belong, are enclosed in parentheses--( . . . ) thus. The genera are here numbered consecutively, in order that the number of genera in each family or each order, in the region, may be readily ascertained (by one process of subtraction), and thus comparisons made with other regions or with any other area. As the tables of birds would be swelled to an inconvenient length by the insertion in each region of all the genera of Waders and Aquatics, most of which have a very wide range and would have to be repeated in several or all the regions, these have been omitted; but a list has been given of such of the genera as are peculiar to, or highly characteristic of each region. As this is the first time that any such extensive tables of {179}distribution have been constructed for the whole of the Mammalia and Birds, they must necessarily contain many errors of detail; but with all their imperfections it is believed they will prove very useful to naturalists, to teachers, and to all who take an intelligent interest in the wider problems of geography and natural history. {180}CHAPTER X. THE PALÆARCTIC REGION. This region is of immense extent, comprising all the temperate portions of the great eastern continents. It thus extends from the Azores and Canary Islands on the west to Japan on the east, a distance not far short of half the circumference of the globe. Yet so great is the zoological unity of this vast tract, that the majority of the genera of animals in countries so far removed as Great Britain and Northern Japan are identical. Throughout its northern half the animal productions of the Palæarctic region are very uniform, except that the vast elevated desert-regions of Central Asia possess some characteristic forms; but in its southern portion, we find a warm district at each extremity with somewhat contrasted features. On the west we have the rich and luxuriant Mediterranean sub-region, possessing many peculiar forms of life, as well as a few which are more especially characteristic of the Ethiopian region. On the east we have the fertile plains of Northern China and the rich and varied islands of Japan, possessing a very distinct set of peculiar forms, with others belonging to the Oriental region, into which this part of the Palæarctic region merges gradually as we approach the Tropic of Cancer. Thus, the countries roughly indicated by the names--Northern Europe, the Mediterranean district, Central and Northern Asia, and China with Japan--have each well-marked minor characteristics which entitle them to the rank of sub-regions. Their boundaries are often indefinable; and those here adopted have been fixed upon to some extent by considerations of convenience, dependent on custom and on the more or less perfect knowledge we possess of some of the intervening countries. [Illustration: PALAEARCTIC REGION] {181}_Zoological Characteristics of the Palæarctic Region._--The Palæarctic region has representatives of thirty-five families of mammalia, fifty-five of birds, twenty-five of reptiles, nine of amphibia, and thirteen of freshwater fishes. Comparing it with the only other wholly temperate region, the Nearctic, we find a much greater variety of types of mammalia and birds. This may be due in part to its greater area, but more, probably, to its southern boundary being conterminous for an enormous distance with two tropical regions, the Ethiopean and Oriental; whereas the Nearctic has a comparatively short southern boundary conterminous with the Neotropical region only. This is so very important a difference, that it is rather a matter of surprise that the two north temperate regions should not be more unequal in the number of their higher vertebrate forms, than they actually are. It is also to the interblending of the Palæarctic with the two adjacent tropical regions, that we must attribute its possession of so few peculiar family groups. These are only three; two of reptiles, _Trogonophidæ_ and _Ophiomoridæ_, and one of fishes, _Comephoridæ_. The number of peculiar genera is, however, considerable, as the following enumeration will show. _Mammalia._--The monkey of Gibraltar and North Africa, and an allied species found in Japan, are now considered to belong to the extensive eastern genus _Macacus_. The former, however, is peculiar in the entire absence of the tail, and has by many naturalists, been held to form a distinct genus, _Inuus_, confined to the Palæarctic region. Of bats there are one or two genera (_Barbastellus_, _Plecotus_) which seem to be mainly or wholly Palæarctic, but the classification of these animals is in such an unsettled state that the distribution of the genera is of little importance. In the next order, Insectivora, we have almost the entire family of the Moles confined to the region. _Talpa_ just enters Northern India; and _Urotrichus_ is common to Japan and {182}North-Western America, but the remaining genera, six in number, are all exclusively Palæarctic. Among Carnivora we have _Nyctereutes_, the curious racoon-dog of Japan and North-Eastern Asia; _Lutronectes_, an otter peculiar to Japan; and the badger (_Meles_), which ranges over the whole region, and just enters the Oriental region as far as Hongkong; _Æluropus_, a curious form of the Himalayan panda, inhabiting the high mountains of Eastern Thibet; and _Pelagius_, a genus of seals, ranging from the shores of Madeira to the Black Sea. The Ungulata, or hoofed animals, are still more productive of forms peculiar to this region. First we have the Camels, whose native home is the desert region of Central and Western Asia and Northern Africa, and which, even in their domesticated condition, are confined almost wholly within the limits of the Palæarctic region. Of Deer we have six peculiar genera, _Dama_ and _Capreolus_ found in Europe, with _Elaphodus_, _Lophotragus_, _Hydropotes_, and _Moschus_, confined to Northern China and Mongolia. The great family Bovidæ--comprising the oxen, sheep, goats and antelopes--furnishes no less than seven peculiar Palæarctic genera. These are _Poephagus_, the yak of Thibet; _Addax_, a well-known antelope of Northern Africa and Syria; _Procapra_, _Pantholops_ and _Budorcas_, antelopine genera peculiar to Thibet and Mongolia; with _Rupicapra_ (the chamois), and the extraordinary large-nosed antelope _Saiga_, confined to Europe and Western Asia. Besides these we have _Capra_ (the wild sheep and goats), all the numerous species of which, except two, are exclusively Palæarctic. Coming to the Rodents, we have again many peculiar forms. Of Muridæ (the mouse and rat tribe), we have six peculiar genera, the more important being _Cricetus_, _Rhombomys Sminthus_, and _Myospalax_. Of Spalacidæ (mole-rats) both the Palæarctic genera, _Ellobius_ and _Spalax_, are peculiar. _Ctenodactylus_, a genus of the South American family Octodontidæ, is found only in North Africa. To these we may add _Myoxus_ (the dormice) and _Lagomys_ (the pikas or tail-less hares) as essentially Palæarctic, since but one species of each genus is found beyond the limits of the region. _Birds._--It appears to have been the opinion of many {183}naturalists that the Palæarctic region could not be well characterised by its peculiar genera of birds. In Mr. Sclater's celebrated paper already referred to, he remarks, "It cannot be denied that the ornithology of the Palæarctic region is more easily characterised by what it has not than by what it has," and this has been quite recently quoted by Mr. Allen, in his essay on the distribution of North American birds, as if it represented our present knowledge of the subject. But, thanks to the labours of Dr. Jerdon, Mr. Swinhoe, Père David and others, we have now learnt that a large number of birds included in the Indian list, are either mere winter emigrants from Central Asia, or only inhabit the higher ranges of the Himalayas, and thus really belong to the Palæarctic region. The result is, that a host of genera are now seen to be either exclusively or characteristically Palæarctic, and we have no further difficulty in giving positive ornithological characters to the region. In the tables appended to this chapter, all these truly Palæarctic genera will be found printed in _italics_, with an indication of their distribution, which will sometimes be found more fully given under the respective families in the fourth part of this work. Referring to this table for details we shall here summarise the results. Of the Sylviidæ or warblers, no less than fourteen genera are either exclusively or characteristically Palæarctic, of which _Locustella_, _Sylvia_, _Curruca_ and _Erithacus_ are good examples. Of the oriental family Timaliidæ, the genus _Pterorhinus_ is Palæarctic. Of Panuridæ, or reedlings, there are four peculiar genera (comprising almost the whole family); of Certhiidæ, or creepers, one--_Tichodroma_--which extends southward to the Abyssinian highlands. Of Paridæ, or tits, one--_Acredula_; of Corvidæ, or crows, four--_Pica_ (containing our magpie) being a good example; of Fringillidæ, or finches and buntings, twelve, among which _Acanthis_, _Pyrrhula_ and _Emberiza_ are good illustrations; of Alaudidæ, or larks, there are two peculiar genera. Leaving the Passeres we next come to peculiar forms among the gallinaceous birds: _Syrrhaptes_ among the Pteroclidæ or sand grouse; four genera of Tetraonidæ or grouse and partridges, and five of Phasianidæ or pheasants, comprising some of the most magnificent birds in the world. Lastly {184}among the far-wandering aquatic birds we have no less than five genera which are more especially Palæarctic,--_Ortygometra_, the corn-crake, and _Otis_, the great bustard, being typical examples. We may add to these, several genera almost confined to this region, such as _Garrulus_ (jays), _Fringilla_ (true finches), _Yunx_ (wrynecks) and some others; so that in proportion to its total generic forms a very large number are found to be peculiar or characteristic. This view, of the high degree of speciality of the Palæarctic region, will no doubt be objected to by some naturalists, on the ground that many of the genera reckoned as exclusively Palæarctic are not so, but extend more or less into other regions. It is well, therefore, to consider what principles should guide us in a matter of this kind, especially as we shall have to apply the same rules to each of the other regions. We may remark first, that the limits of the regions themselves are, when not formed by the ocean, somewhat arbitrary, depending on the average distribution of a number of characteristic forms; and that slight local peculiarities of soil, elevation, or climate, may cause the species of one region to penetrate more or less deeply into another. The land boundary between two regions will be, not a defined line but a neutral territory of greater or less width, within which the forms of both regions will intermingle; and this neutral territory itself will merge imperceptibly into both regions. So long therefore as a species or genus does not permanently reside considerably beyond the possible limits of this neutral territory, we should not claim it as an inhabitant of the adjacent region. A consideration of perhaps more importance arises, from the varying extent of the range of a genus, over the area occupied by the region. Some genera are represented by single species existing only in a very limited area; others by numerous species which occupy, entirely or very nearly, the whole extent of the region; and there is every intermediate grade between these extremes. Now, the small localised genera, are always reckoned as among the best examples of types peculiar to a region; while the more wide-spread groups are often denied that character if they extend a little beyond {185}the supposed regional limits, or send one or two, out of a large number of species, into adjacent regions; yet there is some reason to believe that the latter are really more important as characterising a zoological region than the former. In the case of a single isolated species or genus we have a dying-out group; and we have so many cases of discontinuous species of such groups (of which _Urotrichus_ in Japan and British Columbia, _Eupetes_ in Sumatra and New Guinea are examples), that it is quite as probable as not, that any such isolated species has only become peculiar to the region by the recent extinction of an allied form or forms in some other region. On the other hand, a genus consisting of numerous species ranging over an entire region or the greater part of one, is a dominant group, which has most likely been for some time extending its range, and whose origin dates back to a remote period. The slight extension of such a group beyond the limits of the region to which it mainly belongs, is probably a recent phenomenon, and in that case cannot be held in any degree to detract from its value as one of the peculiar forms of that region. The most numerous examples of this class, are those birds of the temperate regions which in winter migrate, either wholly or partially, into adjacent warmer countries. This migration most likely began subsequent to the Miocene period, during that gradual refrigeration of the temperate zones which culminated in the glacial epoch, and which still continues in a mitigated form. Most of the genera, and many even of the species of birds which migrate southwards in winter, have therefore, most likely, always been inhabitants of our present Palæarctic and Nearctic regions; permanent residents during warm epochs, but only able now to maintain their existence by migration in winter. Such groups belong truly to the temperate zones, and the test of this is the fact of their not having any, or very few, representatives, which are permanent residents in the adjacent tropical regions. When there are such representative species, we do not claim them as peculiar to the Northern regions. Bearing in mind these various considerations, it will be found that we have been very moderate in our estimate of the number of genera {186}that may fairly be considered as exclusively or characteristically Palæarctic. _Reptiles and Amphibia._--The Palæarctic region possesses, in proportion to its limited reptilian fauna, a full proportion of peculiar types. We have for instance two genera of snakes, _Rhinechis_ and _Halys_; seven of lizards, _Trigonophis_, _Psammodromus_, _Hyalosaurus_, _Scincus_, _Ophiomorus_, _Megalochilus_, and _Phrynocephalus_; eight of tailed batrachians, _Proteus_, _Salamandra_, _Seiranota_, _Chioglossa_, _Hynobius_, _Onychodactylus_, _Geotriton_, and _Sieboldia_; and eight of tail-less batrachians, _Bombinator_, _Pelobates_, _Didocus_, _Alytes_, _Pelodytes_, _Discoglossus_, _Laprissa_, and _Latonia_. The distribution of these and other Palæarctic genera will be found in our second vol. chap. xix. _Freshwater Fish._--About twenty genera of freshwater fishes are wholly confined to this region, and constitute a feature which ought not to be overlooked in estimating its claim to the rank of a separate primary division of the earth. They belong to the following families:--Percidæ (three genera), _Acerina_, _Percarina_, _Aspro_; Comephoridæ (one genus), _Comephorus_, found only in Lake Baikal; Salmonidæ (three genera), _Brachymystax_, _Luciotrutta_, and _Plecoglossus_; Cyprinodontidæ (one genus), _Tellia_, found only in Alpine pools on the Atlas Mountains; Cyprinidæ (thirteen genera), _Cyprinus_, _Carassus_, _Paraphoxinus_, _Tinca_, _Achilognathus_, _Rhodeus_, _Chondrostoma_, _Pseudoperilampus_, _Ochetebius_, _Aspius_, _Alburnus_, _Misgurnus_, and _Nemachilus_. _Summary of Palæarctic Vertebrata._--Summarising these details, we find that the Palæarctic region possesses thirty-five peculiar genera of mammalia, fifty-seven of birds, nine of reptiles, sixteen of amphibia, and twenty-one of freshwater fishes; or a total of 138 peculiar generic types of vertebrata. Of these, 87 are mammalia and land-birds out of a total of 274 genera of these groups; or rather less than one-third peculiar, a number which will serve usefully to compare with the results obtained in other regions. In our chapter on Zoological Regions we have already pointed out the main features which distinguish the Palæarctic from the Oriental and Ethiopian regions. The details now given will {187}strengthen our view of their radical distinctness, by showing to how considerable an extent the former is inhabited by peculiar, and often very remarkable generic types. _Insects: Lepidoptera._--The Diurnal Lepidoptera, or butterflies, are not very abundant in species, their number being probably somewhat over 500, and these belong to not more than fifty genera. But no less than fifteen of these genera are wholly confined to the region. Nine of the families are represented, as follows:--1. _Danaidæ_; having only a single species in South Europe. 2. _Satyridæ_; well represented, there being more than 100 species in Europe, and three peculiar genera. 3. _Nymphalidæ_; rather poorly represented, Europe having only about sixty species, but there is one peculiar genus. 4. _Libytheidæ_; a very small family, represented by a single species occurring in South Europe. 5. _Nemeobiidæ_; a rather small family, also having only one species in Europe, but which constitutes a peculiar genera. 6. _Lycænidæ_; an extensive family, fairly represented, having about eighty European species; there are two peculiar genera in the Palæarctic region. 7. _Pieridæ_; rather poorly represented with thirty-two European species; two of the genera are, however, peculiar. 8. _Papilionidæ_; very poorly represented in Europe with only twelve species, but there are many more in Siberia and Japan. No less than five of the small number of genera in this family are wholly confined to the region, a fact of much importance, and which to a great extent redeems the character of the Palæarctic region as regard this order of insects. Their names are _Mesapia_, _Hypermnestra_, _Doritis_, _Sericinus_, and _Thais_; and besides these we have _Parnassius_--the "Apollo" butterflies--highly characteristic, and only found elsewhere in the mountains of the Nearctic region. 9. _Hesperidæ_; poorly represented with about thirty European species, and one peculiar genus. Four families of _Sphingina_ occur in the Palæarctic region, and there are several peculiar genera. In the _Zygænidæ_ there are two exclusively European genera, and the extensive genus _Zygæna_ is itself mainly Palæarctic. The small family _Stygiidæ_ has two out of its three genera {188}confined to the Palæarctic region. In the _Ægeriidæ_ the genus _Ægeria_ is mainly Palæarctic. The _Sphingidæ_ have a wider general range, and none of the larger genera are peculiar to any one region. _Coleoptera._--The Palæarctic region is the richest portion of the globe in the great family of _Carabidæ_, or predacious ground-beetles, about 50 of the genera being confined to it, while many others, including the magnificent genus _Carabus_, have here their highest development. While several of the smaller genera are confined to the eastern or western sub-regions, most of the larger ones extend over the whole area, and give it an unmistakable aspect; while in passing from east to west or _vice-versâ_, allied species and genera replace each other with considerable regularity, except in the extreme south-east, where, in China and Japan, some Oriental forms appear, as do a few Ethiopian types in the south-west. Cicindelidæ, or tiger-beetles, are but poorly represented by about 70 species of the genus _Cicindela_, and a single _Tetracha_ in South Europe. Lucanidæ, or stag-beetles, are also poor, there being representatives of 8 genera. One of these, _Æsalus_ (a single species), is peculiar to South Europe, and two others, _Cladognathus_ and _Cyclopthalmus_, are only represented in Japan, China, and Thibet. Cetoniidæ, or rose-chafers, are represented by 13 genera, two of which are peculiar to South Europe (_Tropinota_ and _Heterocnemis_), while _Stalagmosoma_, ranging from Persia to Nubia, and the fine _Dicranocephalus_ inhabiting North China, Corea, and Nipal, may also be considered to belong to it. The genera _Trichius_, _Gnorimus_, and _Osmoderma_ are confined to the two north temperate regions. Buprestidæ, or metallic beetles, are rather abundant in the warmer parts of the region, 27 genera being represented, nine of which are peculiar. By far the larger portion of these are confined to the Mediterranean sub-region. A considerable number also inhabit Japan and China. The Longicorns, or long-horned beetles, are represented by no less than 196 genera, 51 of which are peculiar. They are {189}much more abundant in the southern than the northern half of the region. Several Oriental genera extend to Japan and North China, and a few Ethiopian genera to North Africa. Thirteen genera are confined, to the two north temperate regions. Several large genera, such as _Dorcadion_ (154 species), _Phytæcia_ (85 species), _Pogonochærus_ (22 species), _Agapanthia_ (22 species), and _Vesperus_ (7 species), are altogether peculiar to the Palæarctic region; and with a preponderance of _Leptura_, _Grammoptera_, _Stenocorus_, and several others, strongly characterise it as distinct from the Nearctic and Oriental regions. The other families which are well developed in the Palæarctic regions, are, the Staphylinidæ or rove-beetles, Silphidæ or burying-beetles, Histeridæ or mimic-beetles, Nitidulidæ, Aphodiidæ, Copridæ (especially in South Europe), Geotrupidæ or dung-beetles, Melolonthidæ or chafers, Elateridæ or click-beetles, the various families of Malacoderms and Heteromera, especially Pimeliidæ in the Mediterranean sub-region, Curculionidæ or weevils, the Phytophaga or leaf-eaters, and Cocinellidæ or lady-birds. The number of species of Coleoptera in the western part of the Palæarctic region is about 15,000, and there are probably not more than 2,000 to add to this number from Siberia, Japan, and North China; but were these countries as well explored as Europe, we may expect that they would add at least 5,000 to the number above given, raising the Palæarctic Coleopterous fauna to 20,000 species. As the total number of species at present known to exist in collections is estimated (and perhaps somewhat over-estimated) at 70,000 species, we may be sure that were the whole earth as thoroughly investigated as Europe, the number would be at least doubled, since we cannot suppose that Europe, with the Mediterranean basin, can contain more than one-fifth of the whole of the Coleoptera of the globe. Of the other orders of insects we here say nothing, because in their case much more than in that of the Coleoptera and Lepidoptera, is the disproportion enormous between our knowledge of the European fauna and that of almost all the rest of the globe. {190}They are, therefore, at present of comparatively little use for purposes of geographical distribution, even were it advisable to enter into the subject in a work which will, perhaps, be too much overburdened with details only of interest to specialists. _Land Shells._--These are very numerous in the warmer parts of the region, but comparatively scarce towards the North. South Europe alone possesses over 600 species, whereas there are only 200 in all Northern Europe and Asia. The total number of species in the whole region is probably about 1,250, of which the great majority are Helicidæ; the Operculated families being very poorly represented. Several small genera or sub-genera are peculiar to the region, as _Testacella_ (West Europe and Canaries); _Leucochroa_ (Mediterranean district); _Acicula_ (Europe); _Craspedopoma_ (Atlantic Islands); _Leonia_ (Algeria and Spain); _Pomatias_ (Europe and Canaries); _Cecina_ (Mongolia). The largest genera are _Helix_ and _Clausilia_, which together comprise more than half the species; _Pupa_, very numerous; _Bulimus_ and _Achatina_ in moderate numbers, and all the rest small. _Helix_ is the only genus which contains large and handsome species; _Bulimus_ and _Achatina_, so magnificent in tropical countries, being here represented by small and obscure forms only. _Daudebardia_ is confined to Central and South Europe and New Zealand; _Glandina_ is chiefly South American; _Hyalina_ is only American and European; _Buliminus_ ranges over all the world except America; and the other European genera of Helicidæ are widely distributed. Of the Operculata, _Cyclotus_, _Cyclophorus_, and _Pupina_ extend from the Oriental region into Japan and North China; _Tudoria_ is found in Algeria and the West Indies; _Hydrocena_ is widely scattered, and occurs in South Europe and Japan. The genera of freshwater shells are all widely distributed. THE PALÆARCTIC SUB-REGIONS. The four sub-regions which are here adopted, have been fixed upon as those which are, in the present state of our knowledge, at once the most natural and the only practicable ones. {191}No doubt all of them could be advantageously again subdivided, in a detailed study of the geographical distribution of _species_. But in a general work, which aims at treating all parts of the world with equal fulness, and which therefore is confined almost wholly to the distribution of families and genera, such further subdivision would be out of place. It is even difficult, in some of the classes of animals, to find peculiar or even characteristic genera for the present sub-regions; but they all have well marked climatic and physical differences, and this leads to an assemblage of species and of groups which are sufficiently distinctive. _I. Central and Northern Europe._ This sub-region, which may perhaps be termed the "European," is zoologically and botanically the best known on the globe. It can be pretty accurately defined, as bounded on the south by the Pyrenees, the Alps, the Balkans, the Black Sea, and the Caucasus range; and by the Ural Mountains, or perhaps more correctly the valley of the Irtish and Caspian Sea, on the east; while Ireland and Iceland are its furthest outliers in the west. To the north, it merges so gradually into the Arctic zone that no demarcation is possible. The great extent to which this sub-region is interpenetrated by the sea, and the prevalence of westerly winds bringing warmth and moisture from an ocean influenced by the gulf-stream, give it a climate for the most part genial, and free from extremes of heat and cold. It is thus broadly distinguished from Siberia and Northern Asia generally, where a more extreme and rigorous climate prevails. The whole of this sub-region is well watered, being penetrated by rivers in every direction; and it consists mainly of plains and undulating country of moderate elevation, the chief mountain ranges being those of Scandinavia in the north-west, and the extensive alpine system of Central Europe. But these are both of moderate height, and a very small portion of their surface is occupied either by permanent snow-fields, or by barren uplands inimical to vegetable and animal life. It is, in {192}fact, to these, and the numerous lesser mountains and hills which everywhere diversify the surface of Europe, that the variety and abundance of its animal life is greatly due. They afford the perennial supplies to rivers, and furnish in their valleys and ever varying slopes, stations suited to every form of existence. A considerable area of Central Europe is occupied by uplands of moderate elevation, a comparatively small portion being flat and marshy plains. Most of the northern and much of the central portions of Europe are covered with vast forests of coniferous trees; and these, occupying as they do those tracts where the winter is most severe, supply food and shelter to many animals who could not otherwise maintain their existence. It is probable that the original condition of the greater part, if not the whole, of temperate Europe, except the flat marshes of the river valleys and the sandy downs of the coast, was that of woodland and forest, mostly of deciduous trees, but with a plentiful admixture of such hardy evergreens as holly, ivy, privet, and yew. A sufficient proportion of these primeval woods, and of artificial plantations which have replaced them, fortunately remain, to preserve for us most of the interesting forms of life, which were developed before man had so greatly modified the surface of the earth, and so nearly exterminated many of its original tenants. Almost exactly in proportion to the amount of woodland that still remains in any part of Europe, do we find (other things being equal) the abundance and variety of wild animals; a pretty clear indication that the original condition of the country was essentially that of a forest, a condition which only now exists in the thinly inhabited regions of the north. Although the sub-region we are considering is, for its extent and latitude, richly peopled with animal life, the number of genera altogether peculiar to it is not great. There are, however, several which are very characteristic, and many species, both of the smaller mammalia and of birds, are wholly restricted to it. _Mammalia._--The genera wholly confined to this sub-region are {193}only two. _Myogale_, the desman, is a curious long-snouted Insectivorous animal somewhat resembling the water-rat in its habits. There are two species, one found only on the banks of streams in the French Pyrenees, the other on the great rivers of Southern Russia. The other peculiar genus, _Rupicapra_ (the chamois of the Alps), is found on all the high mountains of Central Europe. Almost peculiar are _Spalax_ (the mole-rat) found only in Eastern Europe and Western Siberia; and _Saiga_, an extraordinary large-nosed antelope which has a nearly similar distribution. Highly characteristic forms, which inhabit nearly every part of the sub-region, are, _Talpa_ (the mole), _Erinaceus_, (the hedgehog), _Sorex_ (the shrew), _Meles_ (the badger), _Ursus_ (the bear), _Canis_ (the wolf and fox), _Mustela_ (the weasel), _Lutra_ (the otter), _Arvicola_ (the vole), _Myoxus_ (the dormouse), and _Lepus_ (the hare and rabbit); while _Bos_ (the wild bull) was, until exterminated by man, no doubt equally characteristic. Other genera inhabiting the sub-region will be found in the list given at the end of this chapter. _Birds._--It is difficult to name the birds that are most characteristic of this sub-region, because so many of the most familiar and abundant are emigrants from the south, and belong to groups that have a different range. There is perhaps not a single genus wholly confined to it, and very few that have not equal claims to be placed elsewhere. Among the more characteristic we may name _Turdus_ (the thrushes), _Sylvia_ (the warblers), _Panurus_ (the reedling), _Parus_ (the tits), _Anthus_ (the pipits), _Motacilla_ (the wagtails), which are perhaps more abundant here than in any other part of the world, _Emberiza_ (the buntings), _Plectrophanes_ (the snow buntings), _Passer_ (the house sparrows), _Loxia_ (the crossbills), _Linota_ (the linnets), _Pica_ (the magpies), _Tetrao_ (grouse), _Lagopus_ (ptarmigan) and many others. I am indebted to Mr. H. E. Dresser, who is personally acquainted with the ornithology of much of the North of Europe, for some valuable notes on the northern range of many European birds. Those which are characteristic of the extreme Arctic zone, extending beyond 70° north latitude, and tolerably abundant, are two falcons (_Falco gyrfalco_ and _F. peregrinus_); {194}the rough-legged buzzard (_Archibuteo lagopus_); the snowy owl (_Nyctea scandiaca_); the raven (_Corvus corax_); three buntings (_Emberiza schæniculus_, _Plectrophanes nivalis_ and _P. calcarata_); a lark (_Otocorys alpestris_); several pipits, the most northern being _Anthus cervinus_; a wagtail (_Budytes cinereocapilla_); a dipper (_Cinclus melanogaster_); a warbler (_Cyanecula suecica_); the wheatear (_Saxicola oenanthe_); and two ptarmigans (_Lagopus albus_ and _L. salicetus_). Most of these birds are, of course, only summer visitors to the Arctic regions, the only species noted as a permanent resident in East Finmark (north of latitude 70°) being the snow-bunting (_Plectrophanes nivalis_). The birds that are characteristic of the zone of pine forests, or from about 61° to 70° north latitude, are very numerous, and it will be sufficient to note the genera and the number of species (where more than one) to give an idea of the ornithology of this part of Europe. The birds of prey are, _Falco_ (three species), _Astur_ (two species), _Buteo_, _Pandion_, _Surnia_, _Bubo_, _Syrnium_, _Asio_, _Nyctala_. The chief Passerine birds are, _Corvus_ (two species), _Pica_, _Garrulus_ (two species), _Nucifraga_, _Bombycilla_, _Hirundo_ (two species), _Muscicapa_ (two species), _Lanius_, _Sturnus_, _Passer_ (two species), _Pyrrhula_, _Carpodacus_, _Loxia_ (two species), _Pinicola_, _Fringilla_ (eight species), _Emberiza_ (five species), _Alauda_, _Anthus_, _Turdus_ (five species), _Ruticilla_, _Pratincola_, _Accentor_, _Sylvia_ (four species), _Hypolais_, _Regulus_, _Phylloscopus_ (two species), _Acrocephalus_, _Troglodytes_, and _Parus_ (six species). Woodpeckers are abundant, _Picus_ (four species), _Gecinus_, and _Yunx_. The kingfisher (_Alcedo_), goatsucker (_Caprimulgus_), and swift (_Cypselus_) are also common. The wood-pigeon (_Columba_) is plentiful. The gallinaceous birds are three grouse, _Tetrao_ (two species) and _Bonasa_, and the common quail (_Coturnix_). The remaining genera and species of temperate or north-European birds, do not usually range beyond the region of deciduous trees, roughly indicated by the parallel of 60° north latitude. Plate I. [Illustration] THE ALPS OF CENTRAL EUROPE, WITH CHARACTERISTIC ANIMALS. {195}_Plate I.--Illustrating the Zoology of Central Europe._--Before considering the distribution of the other classes of vertebrata, it will be convenient to introduce our first illustration, which represents a scene in the Alps of Central Europe, with figures of some of the most characteristic Mammalia and Birds of this sub-region. On the left is the badger (_Meles Taxus_) one of the weasel family, and belonging to a genus which is strictly Palæarctic. It abounds in Central and Northern Europe and also extends into North Asia, but is represented by another species in Thibet and by a third in Japan. The elegantly-formed creatures on the right are chamois (_Rupicapra tragus_), almost the only European antelopes, and wholly confined to the higher mountains, from the Pyrenees to the Carpathians and the Caucasus. The chamois is the only species of the genus, and is thus perhaps the most characteristic European mammal. The bird on the left, above the badgers, is the Alpine chough, (_Fregilus pyrrhocorax_). It is found in the high mountains from the Alps to the Himalayas, and is allied to the Cornish chough, which is still found on our south-western coasts, and which ranges to Abyssinia and North China. The Alpine chough differs in having a shorter bill of an orange colour, and vermilion red feet as in the other species. In the foreground are a pair of ruffs (_Machetes pugnax_) belonging to the Scolopacidæ or snipe family, and most nearly allied to the genus _Tringa_ or sandpiper. This bird is remarkable for the fine collar of plumes which adorns the males in the breeding season, when they are excessively pugnacious. It is the only species of its genus, and ranges over all Europe and much of Northern Asia, migrating in the winter to the plains of India, and even down the east coast of Africa as far as the Cape of Good Hope; but it only breeds in the Palæarctic region, over the greater part of which it ranges. _Reptiles and Amphibia._--There are no genera of reptiles peculiar to this sub-region. Both snakes and lizards are comparatively scarce, there being about fourteen species of the former and twelve of the latter. Our common snake (_Tropidonotus natrix_) extends into Sweden and North Russia, but the viper (_Viperus berus_) goes further north, as far as Archangel (64° N.), and in Scandinavia (67° N.), and is the most Arctic of all known {196}snakes. Of the lizards, _Lacerta stirpium_ (the sand lizard) has the most northerly range, extending into Poland and Northern Russia; and _Anguis fragilis_ (the blind or slow-worm) has almost an equal range. Amphibia, being more adapted to a northern climate, have acquired a more special development, and thus several forms are peculiar to the North European sub-region. Most remarkable is _Proteus_, a singular eel-like aquatic creature with small legs, found only in the subterranean lakes in Carniola and Carinthia; _Alytes_, a curious toad, the male of which carries about the eggs till they are hatched, found only in Central Europe from France to the east of Hungary; and _Pelodytes_, a frog found only in France. Frogs and toads are very abundant all over Europe, the common frog (_Rana temporaria_) extending to the extreme north. The newts (_Triton_) are also very abundant and widely spread, though not ranging so far north as the frogs. The genera _Bombinator_ (a toad-like frog), and _Hyla_ (the tree frog) are also common in Central Europe. _Freshwater Fish._--Two genera of the perch family (Percidæ) are peculiar to this sub-region,--_Percarina_, a fish found only in the river Dniester, and _Aspro_, confined to the rivers of Central Europe. Of the very characteristic forms are, _Gasterosteus_ (stickle-back), which alone forms a peculiar family--Gasterosteidæ; _Perca_, _Acerina_ and _Lucioperca_, genera of the perch family; _Silurus_, a large fish found in the rivers of Cenrtal Europe, of the family Siluridæ; _Esox_ (the pike), of the family Esocidæ; _Cyprinus_ (carp), _Gobio_ (gudgeon), _Leuciscus_ (roach, chub, dace, &c.), _Tinca_ (tench), _Abramus_ (bream), _Alburnus_ (bleak), _Cobitis_ (loach), all genera of the family Cyprinidæ. _Insects--Lepidoptera._--No genera of butterflies are actually confined to this sub-region, but many are characteristic of it. _Parnassius_, _Aporia_, _Leucophasia_, _Colias_, _Melitæa_, _Argynnis_, _Vanessa_, _Limenitis_, and _Chionobas_, are all very abundant and widespread, and give a feature to the entomology of most of the countries included in it. _Coleoptera._--This sub-region is very rich in Carabidæ; the genera _Elaphrus_, _Nebria_, _Carabus_, _Cychrus_, _Pterostichus_, _Amara_, {197}_Trechus_ and _Peryphus_ being especially characteristic. Staphylinidæ abound. Among Lamellicorns the genus _Aphodius_ is most characteristic. Buprestidæ are scarce; Elateridæ more abundant. Among Malacoderms _Telephorus_ and _Malachius_ are characteristic. Curculionidæ abound: _Otiorhyuchus_, _Omias_, _Erirhinus_, _Bagous_, _Rhynchites_ and _Ceutorhynchus_ being very characteristic genera. Of Longicorns _Callidium_, _Dorcadion_, _Pogonochærus_, _Pachyta_ and _Leptura_ are perhaps the best representatives. _Donacia_, _Crioceris_, _Chrysomela_, and _Altica_, are typical Phytophaga; while _Coccinella_ is the best representative of the Securipalpes. _North European Islands._--The British Islands are known to have been recently connected with the Continent, and their animal productions are so uniformly identical with continental species as to require no special note. The only general fact of importance is, that the number of species in all groups is much less than in continental districts of equal extent, and that this number is still farther diminished in Ireland. This may be accounted for by the smaller area and less varied surface of the latter island; and it may also be partly due to the great extent of low land, so that a very small depression would reduce it to the condition of a cluster of small islands capable of supporting a very limited amount of animal life. Yet further, if after such a submergence had destroyed much of the higher forms of life in Great Britain and Ireland, both were elevated so as to again form part of the Continent, a migration would commence by which they would be stocked afresh; but this migration would be a work of time, and it is to be expected that many species would never reach Ireland or would find its excessively moist climate unsuited to them. Some few British species differ slightly from their continental allies, and are considered by many naturalists to be distinct. This is the case with the red grouse (_Lagopus scoticus_) among birds; and a few of the smaller Passeres have also been found to vary somewhat from the allied forms on the Continent, showing that the comparatively short interval since the glacial period, and the slightly different physical conditions dependent on {198}insularity, have sufficed to commence the work of specific modification. There are also a few small land-shells and several insects not yet found elsewhere than in Britain; and even one of the smaller Mammalia--a shrew (_Sorex rusticus_). These facts are all readily explained by the former union of these islands with the Continent, and the alternate depressions and elevations which are proved by geological evidence to have occurred, by which they have been more than once separated and united again in recent times. For the evidence of this elevation and depression, the reader may consult Sir Charles Lyell's _Antiquity of Man_. Iceland is the only other island of importance belonging to this sub-region, and it contrasts strongly with Great Britain, both in its Arctic climate and oceanic position. It is situated just south of the Arctic circle and considerably nearer Greenland than Europe, yet its productions are almost wholly European. The only indigenous land mammalia are the Arctic fox (_Canis lagopus_), and the polar bear as an occasional visitant, with a mouse (_Mus islandicus_), said to be of a peculiar species. Four species of seals visit its shores. The birds are more interesting. According to Professor Newton, ninety-five species have been observed; but many of these are mere stragglers. There are twenty-three land, and seventy-two aquatic birds and waders. Four or five are peculiar species, though very closely related to others inhabiting Scandinavia or Greenland. Only two or three species are more nearly related to Greenland birds than to those of Northern Europe, so that the Palæarctic character of the fauna is unmistakable. The following lists, compiled from a paper by Professor Newton, may be interesting as showing more exactly the character of Icelandic ornithology. 1. Peculiar species.--_Troglodytes borealis_ (closely allied to the common wren, found also in the Faroe Islands); _Falco islandicus_ (closely allied to _F. gyrfalco_); _Lagopus islandorum_ (closely allied to _L. rupestris_ of Greenland). 2. European species resident in Iceland.--_Emberiza nivalis_, _Corvus corax_, _Haliæetus albicilla_, _Rallus aquaticus_, _Hæmatopus ostralegus_, _Cygnus ferus_, _Mergus_ (two species), _Phalacocorax_ (two {199}species), _Sula bassana_, _Larus_ (two species), _Stercorarius catarractes_, _Puffinus anglorum_, _Mergulus alle_, _Uria_ (three species), _Alca torda_. 3. American species resident in Iceland.--_Clangula islandica_, _Histrionicus torquatus_. 4. Annual visitants from Europe.--_Turdus iliacus_, _Ruticilla tithys_, _Saxicola ænanthe_, _Motacilla alba_, _Anthus pratensis_, _Linota linaria_, _Chelidon urbica_, _Hirundo rustica_, _Falco æsalon_, _Surnia nyctea_, _Otus brachyotus_, _Charadrius pluvialis_, _Ægialites hiaticula_, _Strepsilas interpres_, _Phalaropus fulicarius_, _Totanus calidris_, _Limosa_ (species), _Tringa_ (three species), _Calidris arenaria_, _Gallinago media_, _Numenius phæopus_, _Ardea cinerea_, _Anser_ (two species), _Bernicla_ (two species), _Anas_ (four species), _Fuligula marila_, _Harelda glacialis_, _Somateria mollissima_, _Oedemia nigra_, _Sterna macrura_, _Rissa tridactyla_, _Larus luecopterus_, _Stercorarius_ (two species), _Fratercula artica_, _Colymbus_ (two species), _Podiceps cornutus_. 5. Annual visitant from Greenland.--_Falco candicans_. 6.--Former resident, now extinct.--_Alca impennis_ (the great auk). _II.--Mediterranean Sub-region._ This is by far the richest portion of the Palæarctic region, for although of moderate extent much of it enjoys a climate in which the rigours of winter are almost unknown. It includes all the countries south of the Pyrenees, Alps, Balkans, and Caucasus mountains; all the southern shores of the Mediterranean to the Atlas range, and even beyond it to include the extra-tropical portion of the Sahara; and in the Nile valley as far as the second cataract. Further east it includes the northern half of Arabia and the whole of Persia, as well as Beluchistan, and perhaps Affghanistan up to the banks of the Indus. This extensive district is almost wholly a region of mountains and elevated plateaus. On the west, Spain is mainly a table-land of more than 2000 feet elevation, deeply penetrated by extensive valleys and rising into lofty mountain chains. Italy, Corsica, Sardinia, and Sicily, are all very {200}mountainous, and much of their surface considerably elevated. Further east we have all European Turkey and Greece, a mountain region with a comparatively small extent of level plain. In Asia the whole country, from Smyrna through Armenia and Persia to the further borders of Affghanistan, is a vast mountainous plateau, almost all above 2000, and extensive districts above 5000 feet in elevation. The only large tract of low-land is the valley of the Euphrates. There is also some low-land south of the Caucasus, and in Syria the valley of the Jordan. In North Africa the valley of the Nile and the coast plains of Tripoli and Algiers are almost the only exceptions to the more or less mountainous and plateau-like character of the country. Much of this extensive area is now bare and arid, and often even of a desert character; a fact no doubt due, in great part, to the destruction of aboriginal forests. This loss is rendered permanent by the absence of irrigation, and, it is also thought, by the abundance of camels and goats, animals which are exceedingly injurious to woody vegetation, and are able to keep down the natural growth of forests. Mr. Marsh (whose valuable work _Man and Nature_ gives much information on this subject) believes that even large portions of the African and Asiatic deserts would become covered with woods, and the climate thereby greatly improved, were they protected from these destructive domestic animals, which are probably not indigenous to the country. Spain, in proportion to its extent, is very barren; Italy and European Turkey are more woody and luxuriant; but it is perhaps in Asia Minor, on the range of the Taurus, along the shores of the Black Sea, and to the south of the Caucasus range, that this sub-region attains its maximum of luxuriance in vegetation and in animal life. From the Caspian eastward extends a region of arid plains and barren deserts, diversified by a few more fertile valleys, in which the characteristic flora and fauna of this portion of the Palæarctic region abounds. Further east we come to the forests of the Hindoo Koosh, which probably form the limit of the sub-region. Beyond these we enter on the Siberian sub-region to the north, and on the outlying portion of the Oriental region on the south. {201}In addition to the territories now indicated as forming part of the Mediterranean sub-region, we must add the group of Canary Islands off the west coast of Africa which seem to be an extension of the Atlas mountains, and the oceanic groups of Madeira and the Azores; the latter about 1,000 miles from the continent of Europe, yet still unmistakably allied to it both in their vegetable and animal productions. The peculiarities of the faunas of these islands will be subsequently referred to. It seems at first sight very extraordinary, that so large and wide a sea as the Mediterranean should not separate distinct faunas, and this is the more remarkable when we find how very deep the Mediterranean is, and therefore how ancient we may well suppose it to be. Its eastern portion reaches a depth of 2,100 fathoms or 12,600 feet, while its western basin is about 1,600 fathoms or 9,600 feet in greatest depth, and a considerable area of both basins is more than 1,000 fathoms deep. But a further examination shows, that a comparatively shallow sea or submerged bank incloses Malta and Sicily, and that on the opposite coast a similar bank stretches out from the coast of Tripoli leaving a narrow channel the greatest depth of which is 240 fathoms. Here therefore is a broad plateau, which an elevation of about 1,500 feet would convert into a wide extent of land connecting Italy with Africa; while the same elevation would also connect Morocco with Spain, leaving two extensive lakes to represent what is now the Mediterranean Sea, and affording free communication for land animals between Europe and North Africa. That such a state of things existed at a comparatively recent period, is almost certain; not only because a considerable number of identical _species_ of mammalia inhabit the opposite shores of the Mediterranean, but also because numerous remains of three species of elephants have been found in caves in Malta,--now a small rocky island in which it would be impossible for such animals to live even if they could reach it. Remains of hippopotami are also found at Gibraltar, and many other animals of African types in Greece; all indicating means of communication between South Europe and North Africa which no longer exist. (See Chapter VI. pp. 113-115.) {202}_Mammalia._--There are a few groups of Palæarctic Mammalia that are peculiar to this sub-region. Such are, _Dama_, the fallow deer, which is now found only in South Europe and North Africa; _Psammomys_, a peculiar genus of Muridæ, found only in Egypt and Palestine; while _Ctenodactylus_, a rat-like animal classed in the South American family Octodontidæ, inhabits Tripoli. Among characteristic genera not found in other sub-regions, are, _Dysopes_, a bat of the family Noctilionidæ; _Macroscelides_, the elephant shrew, in North Africa; _Genetta_, the civet, in South Europe; _Herpestes_, the ichneumon, in North Africa and (?) Spain; _Hyæna_, in South Europe; _Gazella_, _Oryx_, _Alcephalus_, and _Addax_, genera of antelopes in North Africa and Palestine; _Hyrax_, in Syria; and _Hystrix_, the porcupine, in South Europe. Besides these, the camel and the horse were perhaps once indigenous in the eastern parts of the sub-region; and a wild sheep (_Ovis musmon_) still inhabits Sardinia, Corsica, and the mountains of the south-east of Spain. The presence of the large feline animals--such as the lion, the leopard, the serval, and the hunting leopard--in North Africa, together with several other quadrupeds not found in Europe, have been thought by some naturalists to prove, that this district should not form part of the Palæarctic region. No doubt several Ethiopian groups and species have entered it from the south; but the bulk of its Mammalia still remains Palæarctic, although several of the species have Asiatic rather than European affinities. The _Macacus innuus_ is allied to an Asiatic rather than an African group of monkeys, and thus denotes an Oriental affinity. Ethiopian affinity is apparently shown by the three genera of antelopes, by _Herpestes_, and by _Macroscelides_; but our examination of the Miocene fauna has shown that these were probably derived from Europe originally, and do not form any part of the truly indigenous or ancient Ethiopian fauna. Against these, however, we have the occurrence in North Africa of such purely Palæarctic and non-Ethiopian genera as _Ursus_, _Meles_, _Putorius_, _Sus_, _Cervus_, _Dama_, _Capra_, _Alactaga_; together with actual European or West Asiatic species of _Canis_, _Genetta_, _Felis_, _Putorius_, _Lutra_, many bats, _Sorex_, _Crocidura_, _Crossopus_, _Hystrix_, {203}_Dipus_, _Lepus_, and _Mus_. It is admitted that, as regards every other group of animals, North Africa is Palæarctic, and the above enumeration shows that even in Mammalia, the intermixture of what are now true Ethiopian types is altogether insignificant. It must be remembered, also, that the lion inhabited Greece even in historic times, while large carnivora were contemporary with man all over Central Europe. _Birds._--So many of the European birds migrate over large portions of the region, and so many others have a wide permanent range, that we cannot expect to find more than a few genera, consisting of one or two species, each, confined to a sub-region; and such appear to be, _Lusciniola_ and _Pyrophthalma_, genera of Sylviidæ. But many are characteristic of this, as compared with other Palæarctic sub-regions; such as, _Bradyptetus_, _Aedon_, _Dromoloea_, and _Cercomela_, among Sylviidæ; _Crateropus_ and _Malacocercus_, among Timaliidæ; _Telophonus_ among Laniidæ; _Certhilauda_ and _Mirafra_ among larks; _Pastor_ among starlings; _Upupa_, the hoopoe; _Halycon_ and _Ceryle_ among kingfishers; _Turnix_ and _Caccabis_ among Gallinæ, and the pheasant as an indigenous bird; together with _Gyps_, _Vultur_ and _Neophron_, genera of vultures. In addition to these, almost all our summer migrants spend their winter in some part of this favoured land, mostly in North Africa, together with many species of Central Europe that rarely or never visit us. It follows, that a large proportion of all the birds of Europe and Western Asia are to be found in this sub-region, as will be seen by referring to the list of the genera of the region. Palestine is one of the remote portions of this region which has been well explored by Canon Tristram, and it may be interesting to give his summary of the range of the birds. We must bear in mind that the great depression of the Dead Sea has a tropical climate, which accounts for the presence here only, of such a tropical form as the sun-bird (_Nectarinea osea_). The total number of the birds of Palestine is 322, and of these no less than 260 are European, at once settling the question of the general affinities of the fauna. Of the remainder eleven belong to North and East Asia, four to the Red Sea, and {204}thirty-one to East Africa, while twenty-seven are peculiar to Palestine. It is evident therefore that an unusual number of East African birds have extended their range to this congenial district, but most of these are desert species and hardly true Ethiopians, and do not much interfere with the general Palæarctic character of the whole assemblage. As an illustration of how wide-spread are many of the Palæarctic forms, we may add, that seventy-nine species of land birds and fifty-five of water birds, are common to Palestine and Britain. The Oriental and Ethiopian genera _Pycnonotus_ and _Nectarinea_ are found here, while _Bessornis_ and _Dromolæa_ are characteristically Ethiopian. Almost all the other genera are Palæarctic. Persia is another remote region generally associated with the idea of Oriental and almost tropical forms, but which yet undoubtedly belongs to the Palæarctic region. Mr. Blanford's recent collections in this country, with other interesting information, is summarised in Mr. Elwes's paper on the "Geographical Distribution of Asiatic Birds" (_Proc. Zool. Soc._ 1873, p. 647). No less than 127 species are found also in Europe, and thirty-seven others belong to European genera; seven are allied to birds of Central Asia or Siberia, and fifteen to those of North-East Africa, while only three are purely of Indian affinities. This shows a preponderance of nearly nine-tenths of Palæarctic forms, which is fully as much as can be expected in any country near the limits of a great region. _Reptiles and Amphibia._--The climatal conditions being here more favourable to these groups, and the genera being often of limited range, we find some peculiar, and several very interesting forms. _Rhinechis_, a genus of Colubrine snakes, is found only in South Europe; _Trogonophis_, one of the Amphisbænians--curious snake-like lizards--is known only from North Africa; _Psammosaurus_, belonging to the water lizards (Varanidæ) is found in North Africa and North-West India; _Psammodromus_, a genus of Lacertidæ, is peculiar to South Europe; _Hyalosaurus_, belonging to the family Zonuridæ, is a lizard of especial interest, as it inhabits North Africa while its nearest ally is the _Ophisaurus_ or "glass snake" of North America; the family of {205}the scinks is represented by _Scincus_ found in North Africa and Arabia. Besides these _Seps_, a genus of sand lizards (Sepidæ) and _Agama_, a genus of Agamidæ, are abundant and characteristic. Of Amphibia we have _Seiranota_, a genus of salamanders found only in Italy and Dalmatia; _Chioglossa_, in Portugal, and _Geotriton_, in Italy, belonging to the same family, are equally peculiar to the sub-region. _Freshwater Fish._--One of the most interesting is _Tellia_, a genus of Cyprinodontidæ found only in alpine pools in the Atlas mountains. _Paraphoxinius_, found in South-East Europe, and _Chondrostoma_, in Europe and Western Asia, genera of Cyprimidæ, seem almost peculiar to this sub-region. _Insects--Lepidoptera._--Two genera of butterflies, _Thais_ and _Doritis_, are wholly confined to this sub-region, the former ranging over all Southern Europe, the latter confined to Eastern Europe and Asia Minor. _Anthocharis_ and _Zegris_ are very characteristic of it, the latter only extending into South Russia, while _Danais_, _Charaxes_, and _Libythea_ are tropical genera unknown in other parts of Europe. _Coleoptera._--This sub-region is very rich in many groups of Coleoptera, of which a few only can be noticed here. Among Carabidæ it possesses _Procerus_ and _Procrustes_, almost exclusively, while _Brachinus_, _Cymindis_, _Lebia_, _Graphipterus_, _Scarites_, _Chlænius_, _Calathus_, and many others, are abundant and characteristic. Among Lamellicorns--Copridæ, Glaphyridæ, Melolonthidæ, and Cetoniidæ abound. Buprestidæ are plentiful, the genera _Julodis_, _Acmæodera_, _Buprestis_, and _Sphenoptera_ being characteristic. Among Malacoderms--Cebrionidæ, Lampyridæ, and Malachiidæ abound. The Tenebrioid Heteromera are very varied and abundant, and give a character to the sub-region. The Mylabridæ, Cantharidæ, and Oedemeridæ are also characteristic. Of the immense number of Curculionidæ--_Thylacites_, _Brachycerus_, _Lixus_, and _Acalles_ may be mentioned as among the most prominent. Of Longicorns there are few genera especially characteristic, but perhaps _Prinobius_, _Purpuricenus_, _Hesperophanes_, and _Parmena_ are most so. Of the remaining families, we may mention Clythridæ, Hispidæ, and Cassididæ as being abundant. {206}_The Mediterranean and Atlantic Islands._--The various islands of the Mediterranean are interesting to the student of geographical distribution as affording a few examples of local species of very restricted range, but as a rule they present us with exactly the same forms as those of the adjacent mainland.[6] Their peculiarities do not, therefore, properly come within the scope of this work. The islands of the Atlantic Ocean belonging to this sub-region are, from their isolated position and the various problems they suggest, of much more interest, and their natural history has been carefully studied. We shall therefore give a short account of their peculiar features. Of the three groups of Atlantic islands belonging to this sub-region, the Canaries are nearest to the Continent, some of the islands being only about fifty miles from the coast of Africa. They are, however, separated from the mainland by a very deep channel (more than 5,000 feet), as shown on our general map. The islands extend over a length of 300 miles; they are very mountainous and wholly volcanic, and the celebrated peak of Teneriffe rises to a height of more than 12,000 feet. The small Madeira group is about 400 miles from the coast of Morocco and 600 from the southern extremity of Portugal; and there is a depth of more than 12,000 feet between it and the continent. The Azores are nearly 1,000 miles west of Lisbon. They are quite alone in mid-Atlantic, the most westerly islands being nearer Newfoundland than Europe, and are surrounded by ocean depths of from 12,000 to 18,000 feet. It will be convenient to take these islands first in order. _Azores._--Considering the remoteness of this group from every other land, it is surprising to find as many as fifty-three species of birds inhabiting or visiting the Azores; and still more to {207}find that they are of Palæarctic genera and, with one exception, all of species found either in Europe, North Africa, Madeira, or the Canaries. The exception is a bullfinch peculiar to the islands, but closely allied to a European species. Of land birds there are twenty-two, belonging to twenty-one genera, all European. These genera are _Cerchneis_, _Buteo_, _Asio_, _Strix_, _Turdus_, _Oriolus_, _Erithacus_, _Sylvia_, _Regulus_, _Saxicola_, _Motacilla_, _Plectrophanes_, _Fringilla_, _Pyrrhula_, _Serinus_, _Sturnus_, _Picus_, _Upupa_, _Columba_, _Caccabis_, and _Coturnix_. Besides the bullfinch (_Pyrrhula_) other species show slight differences from their European allies, but not such as to render them more than varieties. The only truly indigenous mammal is a bat of a European species. Nine butterflies inhabit the Azores; eight of them are European species, one North American. Of beetles 212 have been collected, of which no less than 175 are European species; of the remainder, nineteen are found in the Canaries or Madeira, three in South America, while fourteen are peculiar to the islands. Now these facts (for which we are indebted to Mr. Godman's _Natural History of the Azores_) are both unexpected and exceedingly instructive. In most other cases of remote Oceanic islands, a much larger proportion of the fauna is endemic, or consists of peculiar species and often of peculiar genera; as is well shown by the case of the Galapagos and Juan Fernandez, both much nearer to a continent and both containing peculiar genera and species of birds. Now we know that the cause and meaning of this difference is, that in the one case the original immigration is very remote and has never or very rarely been repeated, so that under the unchecked influence of new conditions of life the species have become modified; in the other case, either the original immigration has been recent, or if remote has been so frequently repeated that the new comers have kept up the purity of the stock, and have not allowed time for the new conditions to produce the effect we are sure they would in time produce if not counteracted. For Mr. Godman tells us that many of the birds are modified--instancing the gold-crested wren, blackcap, and rock dove--and he adds, that the {208}modification all tends in one direction--to produce a more sombre plumage, a greater strength of feet and legs, and a more robust bill. We further find, that four of the land-birds, including the oriole, snow-bunting, and hoopoe, are not resident birds, but straggle accidentally to the islands by stress of weather; and we are told that every year some fresh birds are seen after violent storms. Add to this the fact, that the number of species diminishes in the group as we go from east to west, and that the islands are subject to fierce and frequent storms blowing from every point of the compass,--and we have all the facts requisite to enable us to understand how this remote archipelago has become stocked with animal life without ever probably being much nearer to Europe than it is now. For the islands are all volcanic, the only stratified rock that occurs being believed to be of Miocene date. _Madeira and the Canaries._--Coming next to Madeira, we find the number of genera of land birds has increased to twenty-eight, of which seventeen are identical with those of the Azores. Some of the commonest European birds--swallows, larks, sparrows, linnets, goldfinches, ravens, and partridges, are among the additions. A gold-crested warbler, _Regulus Maderensis_, and a pigeon, _Columba Trocaz_, are peculiar to Madeira. In the Canaries we find that the birds have again very much increased, there being more than fifty genera of land birds; but the additions are wholly European in character, and almost all common European species. We find a few more peculiar species (five), while some others, including the wild canary, are common to all the Atlantic Islands or to the Canaries and Madeira. Here, too, the only indigenous mammalia are two European species of bats. _Land Shells._--The land shells of Madeira offer us an instructive contrast to the birds of the Atlantic Islands. About fifty-six species have been found in Madeira, and forty-two in the small adjacent island of Porto Santo, but only twelve are common to both, and all or almost all are distinct from their nearest allies in Europe and North Africa. Great numbers of fossil shells are also found in deposits of the Newer Pliocene period; and {209}although these comprise many fresh species, the two faunas and that of the continent still remain almost as distinct from each other as before. It has been already stated (p. 31) that the means by which land mollusca have been carried across arms of the sea are unknown, although several modes may be suggested; but it is evidently a rare event, requiring some concurrence of favourable conditions not always present. The diversity and specialization of the forms of these animals is, therefore, easily explained by the fact, that, once introduced they have been left to multiply under the influence of a variety of local conditions, which inevitably lead, in the course of ages, to the formation of new varieties and new species. _Coleoptera._--The beetles of Madeira and the Canaries have been so carefully collected and examined by Mr. T. V. Wollaston, and those of the Azores described and compared by Mr. Crotch, and they illustrate so many curious points in geographical distribution, that it is necessary to give some account of them. No less than 1,480 species of beetles have been obtained from the Canaries and Madeira, only 360 of which are European, the remainder being peculiar to the islands. The Canaries are inhabited by a little over 1,000 species, Madeira by about 700, while 240 are common to both; but it is believed that many of these have been introduced by man. In the Azores, 212 species have been obtained, of which 175 are European; showing, as in the birds, as closer resemblance to the European fauna than in the other islands which, although nearer to the continent, offer more shelter and are situated in a less tempestuous zone. Of the non-European species in the Azores, 19 are found also in the other groups of islands, 14 are peculiar, while 3 are American. Of the European species, 132 are found also in the other Atlantic islands, while 43 have reached the Azores only. This is interesting as showing to how great an extent the same insects reach all the islands, notwithstanding the difference of latitude and position; and it becomes of great theoretical importance, when we find how many extensive families and genera are altogether absent. The Madeira group has been more thoroughly explored than {210}any other, and its comparatively remote situation, combined with its luxuriant vegetation, have been favourable to the development and increase of the peculiar forms which characterize all the Atlantic islands in a more or less marked degree. A consideration of some of its peculiarities will, therefore, best serve to show the bearing of the facts presented by the insect fauna of the Atlantic islands, on the general laws of distribution. The 711 species of beetles now known from the Madeira group, belong to 236 genera; and no less than 44 of these genera are not European but are peculiar to the Atlantic islands. Most of them are, however, closely allied to European genera, of which they are evidently modifications. A most curious general feature presented by the Madeiran beetles, is the total absence of many whole families and large genera abundant in South Europe. Such are the Cicindelidæ, or tiger beetles; the Melolonthidæ, or chafers; the Cetoniidæ, or rose-chafers; the Eumolpidæ and Galerucidæ, large families of Phytophagous, or leaf-eating beetles; and also the extensive groups of Elateridæ and Buprestidæ, which are each represented by but one minute species. Of extensive genera abundant in South Europe, but wholly absent in Madeira, are _Carabus_, _Rhizotrogus_, _Lampyris_, and other genera of Malacoderms; _Otiorhynchus_, _Brachycerus_, and 20 other genera of Curculionidæ, comprising more than 300 South European and North African species; _Pimelia_, _Tentyra_, _Blaps_, and 18 other genera of Heteromera, comprising about 550 species in South Europe and North Africa; and _Timarcha_, containing 44 South European and North African species. Another most remarkable feature of the Madeiran Coleoptera is the unusual prevalence of apterous or wingless insects. This is especially the case with groups which are confined to the Atlantic islands, many of which consist wholly of wingless species; but it also affects the others, no less than twenty-two genera which are usually or sometimes winged in Europe, having only wingless species in Madeira; and even the same species which is winged in Europe becomes, in at least three cases, wingless in Madeira, without any other perceptible change having taken place. But there is another most curious fact noticed by {211}Mr. Wollaston; that those species which possess wings in Madeira, often have them rather larger than their allies in Europe. These two facts were connected by Mr. Darwin, who suggested that flying insects are much more exposed to be blown out to sea and lost, than those which do not fly (and Mr. Wollaston had himself supposed that the "stormy atmosphere" of Madeira had something to do with the matter); so that the most frequent fliers would be continually weeded out, while the more sluggish individuals, who either could not or would not fly, remained to continue the race; and this process going on from generation to generation, would, on the well-ascertained principles of selection and abortion by disuse, in time lead to the entire loss of wings by those insects to whom wings were _not a necessity_. But those whose wings were essential to their existence would be acted upon in another way. All these must fly to obtain their food or provide for their offspring, and those that flew best would be best able to battle with the storms, and keep themselves safe, and thus those with the longest and most powerful wings would be preserved. If however all the individuals of the species were too weak on the wing to resist the storms, they would soon become extinct.[7] Now this explanation of the facts is not only simple and probable in itself, but it also serves to explain in a remarkable manner some of the peculiarities and deficiencies of the Madeiran insect fauna, in harmony with the view (supported by the distribution of the birds and land shells, and in particular by the immigrant birds and insects of the Azores) that all the insects have been derived from the continent or from other islands, by {212}immigration across the ocean, in various ways and during a long period. These deficiencies are, on the other hand, quite inconsistent with the theory (still held by some entomologists) that a land communication is absolutely necessary to account for the origin of the Madeiran fauna. First, then, we can understand how the tiger-beetles (Cicindelidæ) are absent; since they are insects which have a short weak flight, but yet to whom flight is necessary. If a few had been blown over to Madeira, they would soon have become exterminated. The same thing applies to the Melolonthidæ, Cetoniidæ, Eumolpidæ, and Galerucidæ,--all flower and foliage-haunting insects, yet bulky and of comparatively feeble powers of flight. Again, all the large genera abundant in South Europe, which have been mentioned above as absent from Madeira, are wholly apterous (or without wings), and thus their absence is a most significant fact; for it proves that in the case of all insects of moderate size, flight was essential to their reaching the island, which could not have been the case had there been a land connection. There are, however, one or two curious exceptions to the absence of these wholly apterous European genera in Madeira, and as in each case the reason of their being exceptions can be pointed out, they are eminently exceptions that prove the rule. Two of the apterous species common to Europe and Madeira are found always in ants' nests; and as ants, when winged, fly in great swarms and are carried by the wind to great distances, they may have conveyed the minute eggs of these very small beetles. Two European species of _Blaps_ occur in Madeira, but these are house beetles, and are admitted to have been introduced by man. There are also three species of _Meloe_, of which two are European and one peculiar. These are large, sluggish, wingless insects, but they have a most extraordinary and exceptional metamorphosis, the larvae in the first state being minute active insects parasitic on bees, and thus easily conveyed across the ocean. This case is most suggestive, as it accounts for what would be otherwise a difficult anomaly. Another case, not quite so easily explained, is that of the genus _Acalles_, which is very abundant in all the Atlantic {213}islands and also occurs in South Europe, but is always apterous. It is however closely allied to another genus, _Cryptorhynchus_, which is apterous in some species, winged in others. We may therefore well suppose that the ancestors of _Acalles_ were once in the same condition, and that some of the winged forms reached Madeira, the genus having since become wholly apterous. We may look at this curious subject in another way. The Coleoptera of Madeira may be divided into those which are found also in Europe or the other islands, and those which are peculiar to it. On the theory of introduction by accidental immigration across the sea, the latter must be the more ancient, since they have had time to become modified; while the former are comparatively recent, and their introduction may be supposed to be now going on. The peculiar influence of Madeira in aborting the wings should, therefore, have acted on the ancient and changed forms much more powerfully than on the recent and unchanged forms. On carefully comparing the two sets of insects (omitting those which have almost certainly been introduced by man) we find, that out of 263 species which have a wide range, only 14 are apterous; while the other class, consisting of 393 species, has no less than 178 apterous; or about 5 per cent in the one case, and 45 per cent in the other.[8] On the theory of a land connection as the main agent in introducing the fauna, both groups must have been introduced at or about the same time, and why one set should have lost their wings and the other not, is quite inexplicable. Taking all these singular facts, in connection with the total absence of all truly indigenous terrestrial mammalia and reptiles from these islands--even from the extensive group of the Canaries so comparatively near to the continent, we are forced to reject the theory of a land connection as quite untenable; and this view becomes almost demonstrated by the case of the Azores, which being so much further off, and surrounded by such a vast expanse of deep ocean, could only have been {214}connected with Europe at a far remoter epoch, and ought therefore to exhibit to us a fauna composed almost entirely of peculiar forms both of birds and insects. Yet, so far from this being the case, the facts are exactly the reverse. Far more of the birds and insects are identical with those of Europe than in the other islands, and this difference is clearly traced to the more tempestuous atmosphere, which is shown to be even now annually bringing fresh immigrants (both birds and insects) to its shores. We here see nature actually at work; and if the case of Madeira rendered her mode of action probable, that of the Azores may be said to demonstrate it. Mr. Wollaston has objected to this view that "storms and hurricanes" are somewhat rare in the latitude of Madeira and the Canaries; but this little affects the question, since the _time_ allowed for such operations is so ample. If but one very violent storm happened in a century, and ten such storms recurred before a single species of insect was introduced into Madeira, that would be more than sufficient to people it, as we now find it, with a varied fauna. But he also adds the important information that the ordinary winds blow almost uninterruptedly from the north-east, so that there would be always a chance of a little stronger wind than usual bringing insect, or larva, or egg, attached to leaves or twigs. Neither Mr. Wollaston, Mr. Crotch, Mr. A. Murray, nor any other naturalist who upholds the land-connection theory, has attempted to account for the fact of the absence of so many extensive groups of insects that ought to be present, as well as of all small mammalia and reptiles. _Cape Verd Islands._--There is yet another group of Atlantic islands which is very little known, and which is usually considered to be altogether African--the Cape Verd Islands, situated between 300 and 400 miles west of Senegal, and a little to the south of the termination of the Sahara. The evidence that we possess as to the productions of these islands, shows that, like the preceding groups, they are truly oceanic, and have probably derived their fauna from the desert and the Canaries to the north-east of them rather than from the fertile and more truly {215}Ethiopian districts of Senegal and Gambia to the east. There is a mingling of the two faunas, but the preponderance seems to be undoubtedly with the Palæarctic rather than with the Ethiopian. I owe to Mr. R. B. Sharpe of the British Museum, a MS. list of the birds of these islands, twenty-three species in all. Of these eight are of wide distribution and may be neglected. Seven are undoubted Palæarctic species, viz.:--_Milvus ictinus_, _Sylvia atricapilla_, _S. conspicillata_, _Corvus corone_, _Passer salicarius_, _Certhilauda desertorum_, _Columba livia_. Three are peculiar species, but of Palæarctic genera and affinities, viz.:--_Calamoherpe brevipennis_, _Ammomanes cinctura_, and _Passer jagoensis_. Against this we have to set two West African species, _Estrilda cinerea_ and _Numida meleagris_, both of which were probably introduced by man; and three which are of Ethiopian genera and affinities, viz.:--_Halcyon erythrorhyncha_, closely allied to _H. semicærulea_ of Arabia and North-east Africa, and therefore almost Palæarctic; _Accipiter melanoleucus_; and _Pyrrhulauda nigriceps_, an Ethiopian form; but the same species occurs in the Canaries. The Coleoptera of these islands have been also collected by Mr. Wollaston, and he finds that they have generally the same European character as those of the Canaries and Madeira, several of the peculiar Atlantic genera, such as _Acalles_ and _Hegeter_, occurring, while others are represented by new but closely allied genera. Out of 275 species 91 were found also in the Canaries and 81 in the Madeiran group; a wonderful amount of similarity when we consider the distance and isolation of these islands and their great diversity of climate and vegetation. This connection of the four groups of Atlantic islands now referred to, receives further support from the occurrence of land-shells of the subgenus _Leptaxis_ in all the groups, as well as in Majorca; and by another subgenus, _Hemicycla_, being common to the Canaries and Cape Verd islands. Combining these several classes of facts, we seem justified in extending the Mediterranean sub-region to include the Cape Verd Islands. {216}_III.--The Siberian Sub-region, or Northern Asia._ This large and comparatively little-known subdivision of the Palæarctic region, extends from the Caspian Sea to Kamschatka and Behring's Straits, a distance of about 4,000 miles; and from the shores of the Arctic Ocean to the high Himalayas of Sikhim in North Latitude 29°, on the same parallel as Delhi. To the east of the Caspian Sea and the Ural Mountains is a great extent of lowland which is continued round the northern coast, becoming narrower as it approaches the East Cape. Beyond this, in a general E.N.E. direction, rise hills and uplands, soon becoming lofty mountains, which extend in an unbroken line from the Hindu Koosh, through the Thian Shan, Altai and Yablonoi Mountains, to the Stanovoi range in the north-eastern extremity of Asia. South of this region is a great central basin, which is almost wholly desert; beyond which again is the vast plateau of Thibet, with the Kuenlun, Karakorum, and Himalayan snow-capped ranges, forming the most extensive elevated district on the globe. The superficial aspects of this vast territory, as determined by its vegetable covering, are very striking and well contrasted. A broad tract on the northern coast, varying from 150 to 300 and even 500 miles wide, is occupied by the Tundras or barrens, where nothing grows but mosses and the dwarfest Arctic plants, and where the ground is permanently frozen to a great depth. This tract has its greatest southern extension between the rivers Obi and Yenesi, where it reaches the parallel of 60° north latitude. Next to this comes a vast extent of northern forests, mostly of conifers in the more northern and lofty situations, while deciduous trees preponderate in the southern portions and in the more sheltered valleys. The greatest extension of this forest region is north of Lake Baikal, where it is more than 1,200 miles wide. These forests extend along the mountain ranges to join those of the Hindu Koosh. South of the forests the remainder of the sub-region consists of open pasture-lands and vast intervening deserts, of which the Gobi, and those of Turkestan between the Aral and Balkash lakes, are the most {217}extensive. The former is nearly 1,000 miles long, with a width of from 200 to 350 miles, and is almost as complete a desert as the Sahara. With very few exceptions, this vast territory is exposed to an extreme climate, inimical to animal life. All the lower parts being situated to the north, have an excessively cold winter, so that the limit of constantly frozen ground descends below the parallel of 60° north latitude. To the south, the land is greatly elevated, and the climate extremely dry. In summer the heat is excessive, while the winter is almost as severe as further north. The whole country, too, is subject to violent storms, both in summer and winter; and the rich vegetation that clothes the steppes in spring, is soon parched up and replaced by dusty plains. Under these adverse influences we cannot expect animal life to be so abundant as in those sub-regions subject to more favourable physical conditions; yet the country is so extensive and so varied, that it does actually, as we shall see, possess a very considerable and interesting fauna. _Mammalia._--Four genera seem to be absolutely confined to this sub-region, _Nectogale_, a peculiar form of the mole family (Talpidæ); _Poephagus_, the yak, or hairy bison of Thibet; with _Procapra_ and _Pantholops_, Thibetan antelopes. Some others more especially belong here, although they just enter Europe, as _Saiga_, the Tartarian antelope; _Sminthus_, a desert rat;, and _Ellobius_, a burrowing mole-rat; while _Myospalax_, a curious rodent allied to the voles, is found only in the Altai mountains and North China; and _Moschus_, the musk-deer, is almost confined to this sub-region. Among the characteristic animals of the extreme north, are _Mustela_, and _Martes_, including the ermine and sable; _Gulo_, the glutton; _Tarandus_, the reindeer; _Myodes_, the lemming; with the lynx, arctic fox, and polar bear; and here, in the Post-pliocene epoch, ranged the hairy rhinoceros and Siberian mammoth, whose entire bodies still remain preserved in the ice-cliffs near the mouths of the great rivers. Farther south, species of wild cat, bear, wolf, deer, and pika (_Lagomys_) abound; while in the mountains we find wild goats and sheep of several species, and in the plains and deserts wild horses {218}and asses, gazelles, two species of antelopes, flying squirrels (_Pteromys_), ground squirrels (_Tamias_), marmots, of the genus _Spermophilus_, with camels and dromedaries, probably natives of the south-western part of this sub-region. The most abundant and conspicuous of the mammalia are the great herds of reindeer in the north, the wolves of the steppes, with the wild horses, goats, sheep, and antelopes of the plateaus and mountains. Among the curiosities of this sub-region we must notice the seal, found in the inland and freshwater lake Baikal, at an elevation of about 2,000 feet above the sea. It is a species of _Callocephalus_, closely allied to, if not identical with, one inhabiting northern seas as well as the Caspian and Lake Aral. This would indicate that almost all northern Asia was depressed beneath the sea very recently; and Mr. Belt's view, of the ice during the glacial epoch having dammed up the rivers and converted much of Siberia into a vast freshwater or brackish lake, perhaps offers the best solution of the difficulty.[9] _Plate II.--Characteristic Mammalia of Western Tartary._--Several of the most remarkable animals of the Palæarctic region inhabit Western Tartary, and are common to the European and Siberian sub-regions. We therefore choose this district for one of our illustrative plates. The large animals in the centre are the remarkable saiga antelopes (_Saiga Tartarica_), distinguished from all others by a large and fleshy proboscis-like nose, which gives them a singular appearance. They differ so much from all other antelopes that they have been formed into a distinct family by some naturalists, but are here referred to the great family Bovidæ. They inhabit the open plains from Poland to the Irtish River. On the left is the mole-rat, or sand-rat (_Spalax murinus_). This animal burrows under ground like a mole, feeding on bulbous roots. It inhabits the same country as the saiga, but extends farther south in Europe. On the right is a still more curious animal, the desman (_Myogale Muscovitica_), a long-snouted water-mole. This creature is fifteen inches long, including the tail; it burrows in the banks of streams, feeding on insects, {219}worms, and leeches; it swims well, and remains long under water, raising the tip of the snout, where the nostrils are situated, to the surface when it wants to breathe. It is thus well concealed; and this may be one use of the development of the long snout, as well as serving to follow worms into their holes in the soft earth. This species is confined to the rivers Volga and Don in Southern Russia, and the only other species known inhabits some of the valleys on the north side of the Pyrenees. In the distance are wolves, a characteristic feature of these wastes. Plate II. [Illustration] CHARACTERISTIC MAMMALIA OF WESTERN TARTARY. _Birds._--But few genera of birds are absolutely restricted to this sub-region. _Podoces_, a curious form of starling, is the most decidedly so; _Mycerobas_ and _Pyrrhospiza_ are genera of finches confined to Thibet and the snowy Himalayas; _Leucosticte_, another genus of finches, is confined to the eastern half of the sub-region and North America; _Tetraogallus_, a large kind of partridge, ranges west to the Caucasus; _Syrrhaptes_, a form of sand-grouse, and _Lerwa_ (snow-partridge), are almost confined here, only extending into the next sub-region; as do _Grandala_, and _Calliope_, genera of warblers, _Uragus_, a finch allied to the North American cardinals, and _Crossoptilon_, a remarkable group of pheasants. Almost all the genera of central and northern Europe are found here, and give quite a European character to the ornithology, though a considerable number of the species are different. There are a few Oriental forms, such as _Abrornis_ and _Larvivora_ (warblers); with _Ceriornis_ and _Ithaginis_, genera of pheasants, which reach the snow-line in the Himalayas and thus just enter this sub-region, but as they do not penetrate farther north, they hardly serve to modify the exclusively Palæarctic character of its ornithology. According to Middendorf, the extreme northern Asiatic birds are the Alpine ptarmigan (_Lagopus mutus_); the snow-bunting (_Plectrophanes nivalis_); the raven, the gyrfalcon and the snowy-owl. Those which are characteristic of the barren "tundras," but which do not range so far north as the preceding are,--the willow-grouse (_Lagopus albus_); the Lapland-bunting (_Plectrophanes {220}lapponica_); the shore-lark (_Otocorys alpestris_); the sand-martin (_Cotyle riparia_), and the sea-eagle (_Haliæetus albicilla_). Those which are more characteristic of the northern forests, and which do not pass beyond them, are--the linnet; two crossbills (_Loxia Leucoptera_ and _L. Curvirostra_); the pine grosbeak (_Pinicola enucleator_); the waxwing; the common magpie; the common swallow; the peregrine falcon; the rough-legged buzzard; and three species of owls. Fully one-half of the land-birds of Siberia are identical with those of Europe, the remainder being mostly representative species peculiar to Northern Asia, with a few stragglers and immigrants from China and Japan or the Himalayas. A much larger proportion of the wading and aquatic families are European or Arctic, these groups having always a wider range than land birds. _Reptiles and Amphibia._--From the nature of the country and climate these are comparatively few, but in the more temperate districts snakes and lizards seem to be not uncommon. _Halys_, a genus of Crotaline snakes, and _Phrynocephalus_, lizards of the family Agamidæ, are characteristic of these parts. _Simotes_, a snake of the family Oligodontidæ, reaches an elevation of 16,000 feet in the Himalayas, and therefore enters this sub-region. _Insects._--_Mesapia_ and _Hypermnestra_, genera of Papilionidæ, are butterflies peculiar to this sub-region; and _Parnassius_ is as characteristic as it is of our European mountains. Carabidæ are also abundant, as will be seen by referring to the Chapter on the Distribution of Insects in the succeeding part of this work. The insects, on the whole, have a strictly European character, although a large proportion of the species are peculiar, and several new genera appear. _IV.--Japan and North China, or the Manchurian Sub-region._ This is an interesting and very productive district, corresponding in the east to the Mediterranean sub-region in the west, or rather perhaps to all western temperate Europe. Its limits are not very well defined, but it probably includes all Japan; the Corea and Manchuria to the Amour river and to the lower {221}slopes of the Khingan and Peling mountains; and China to the Nanlin mountains south of the Yang-tse-kiang. On the coast of China the dividing line between it and the Oriental region seems to be somewhere about Foo-chow, but as there is here no natural barrier, a great intermingling of northern and southern forms takes place. Japan is volcanic and mountainous, with a fine climate and a most luxuriant and varied vegetation. Manchuria is hilly, with a high range of mountains on the coast, and some desert tracts in the interior, but fairly wooded in many parts. Much of northern China is a vast alluvial plain, backed by hills and mountains with belts of forest, above which are the dry and barren uplands of Mongolia. We have a tolerable knowledge of China, of Japan, and of the Amoor valley, but very little of Corea and Manchuria. The recent researches of Père David in Moupin, in east Thibet, said to be between 31° and 32° north latitude, show, that the fauna of the Oriental region here advances northward along the flanks of the Yun-ling mountains (a continuation of the Himalayas); since he found at different altitudes representatives of the Indo-Chinese, Manchurian, and Siberian faunas. On the higher slopes of the Himalayas, there must be a narrow strip from about 8,000 to 11,000 feet elevation intervening between the tropical fauna of the Indo-Chinese sub-region and the almost arctic fauna of Thibet; and the animals of this zone will for the most part belong to the fauna of temperate China and Manchuria, except in the extreme west towards Cashmere, where the Mediterranean fauna will in like manner intervene. On a map of sufficiently large scale, therefore, it would be necessary to extend our present sub-region westward along the Himalayas, in a narrow strip just below the upper limits of forests. It is evident that the large number of Fringillidæ, Corvidæ, Troglodytidæ, and Paridæ, often of south Palæarctic forms, that abound in the higher Himalayas, are somewhat out of place as members of the Oriental fauna, and are equally so in that of Thibet and Siberia; but they form a natural portion of that of North China on the one side, or of South Europe on the other. {222}_Mammalia._--This sub-region contains a number of peculiar and very interesting forms, most of which have been recently discovered by Père David in North and West China and East Thibet. The following are the peculiar genera:--_Rhinopithecus_, a sub-genus of monkeys, here classed under _Semnopithecus_; _Anurosorex_, _Scaptochirus_, _Uropsilus_ and _Scaptonyx_, new forms of Talpidæ or moles; _Æluropus_ (Æluridæ); _Nyctereutes_ (Canidæ); _Lutronectes_ (Mustelidæ); _Cricetulus_ (Muridæ); _Hydropotes_, _Moschus_, and _Elaphodus_ (Cervidæ). The _Rhinopithecus_ appears to be a permanent inhabitant of the highest forests of Moupin, in a cold climate. It has a very thick fur, as has also a new species of _Macacus_ found in the same district. North China and East Thibet seem to be very rich in Insectivora. _Scaptochirus_ is like a mole; _Uropsilus_ between the Japanese _Urotrichus_ and _Sorex_; _Scaptonyx_ between _Urotrichus_ and _Talpa_. _Æluropus_ seems to be the most remarkable mammal discovered by Père David. It is allied to the singular panda (_Ælurus fulgens_) of Nepal, but is as large as a bear, the body wholly white, with the feet, ears, and tip of the tail black. It inhabits the highest forests, and is therefore a true Palæarctic animal, as most likely is the _Ælurus_. _Nyctereutes_, a curious racoon-like dog, ranges from Canton to North China, the Amoor and Japan, and therefore seems to come best in this sub-region; _Hydropotes_ and _Lophotragus_ are small hornless deer confined to North China; _Elaphodus_, from East Thibet, is another peculiar form of deer; while the musk deer (_Moschus_) is confined to this sub-region and the last. Besides the above, the following Palæarctic genera were found by Père David in this sub-region: _Macacus_: five genera or sub-genera of bats (_Vespertilio_, _Vesperus_, _Vesperugo_, _Rhinolophus_, and _Murina_); _Erinaceus_, _Nectogale_, _Talpa_, _Crocidura_ and _Sorex_, among Insectivora; _Mustela_, _Putorius_, _Martes_, _Lutra_, _Viverra_, _Meles_, _Ælurus_, _Ursus_, _Felis_, and _Canis_, among _Carnivora_; _Hystrix_, _Arctomys_, _Myospalax_, _Spermophilus_, _Gerbillus_, _Dipus_, _Lagomys_, _Lepus_, _Sciurus_, _Pteromys_, _Arvicola_, and _Mus_, among Rodentia; _Budorcas_, _Nemorhedus_, _Antilope_, _Ovis_, _Moschus_, _Cervulus_ and _Cervus_ among Ruminants; and the wide-spread _Sus_ or wild boar. The following Oriental genera are also {223}included in Père David's list, but no doubt occur only in the lowlands and warm valleys, and can hardly be considered to belong to the Palæarctic region: _Paguma_, _Helictis_, _Arctonyx_, _Rhizomys_, _Manis_. The _Rhizomys_ from Moupin is a peculiar species of this tropical genus, but all the others inhabit Southern China. A few additional forms occur in Japan: _Urotrichus_, a peculiar Mole, which is found also in north-west America; _Enhydra_, the sea otter of California; and the dormouse (_Myoxus_). Japan also possesses peculiar species of _Macacus_, _Talpa_, _Meles_, _Canis_, and _Sciuropterus_. It will be seen that this sub-region is remarkably rich in Insectivora, of which it possesses ten genera; and that it has also several peculiar forms of Carnivora, Rodentia, and Ruminants. _Birds._--To give an accurate idea of the ornithology of this sub-region is very difficult, both on account of its extreme richness and the impossibility of defining the limits between it and the Oriental region. A considerable number of genera which are well developed in the high Himalayas, and some which are peculiar to that district, have hitherto always been classed as Indian, and therefore Oriental groups; but they more properly belong to this sub-region. Many of them frequent the highest forests, or descend into the Himalayan temperate zone only in winter; and others are so intimately connected with Palæarctic species, that they can only be considered as stragglers into the border land of the Oriental region. On these principles we consider the following genera to be confined to this sub-region:-- _Grandala_, _Nemura_ (Sylviidæ); _Pterorhinus_ (Timaliidæ); _Cholornis_, _Conostoma_, _Heteromorpha_ (Panuridæ); _Cyanoptila_ (Muscicapidæ); _Eophona_ (Fringillidæ); _Dendrotreron_ (Columbidæ); _Lophophorus_, _Tetraophasis_, _Crossoptilon_, _Pucrasia_, _Thaumalea_, and _Ithaginis_ (Phasianidæ). This may be called the sub-region of Pheasants; for the above six genera, comprising sixteen species of the most magnificent birds in the world, are all confined to the temperate or cold mountainous regions of the Himalayas, Thibet, and China; and in addition we have {224}most of the species of tragopan (_Ceriornis_), and some of the true pheasants (_Phasianus_). The most abundant and characteristic of the smaller birds are warblers, tits, and finches, of Palæarctic types; but there are also a considerable number of Oriental forms which penetrate far into the country, and mingling with the northern birds give a character to the Ornithology of this sub-region very different from that of the Mediterranean district at the western end of the region. Leaving out a large number of wide-ranging groups, this mixture of types may be best exhibited by giving lists of the more striking Palæarctic and Oriental genera which are here found intermingled. PALÆARCTIC GENERA. SYLVIIDÆ. Erithacus. Ruticilla. Locustella. Cyanecula. Sylvia. Potamodus. Reguloides. Regulus. Accentor. CINCLIDÆ. Cinclus. TROGLODYTIDÆ. Troglodytidæ. CERTHIIDÆ. Certhia. Sitta. Tichodroma. PARIDÆ. Parus. Lophophanes. Acredula. CORVIDÆ. Fregilus. Nucifraga. Pica. Cyanopica. Garrulus. AMPELIDÆ. Ampelis. FRINGILLIDÆ. Fringilla. Chrysomitris. Chlorospiza. Passer. Coccothraustes. Pyrrhula. Carpodacus. Uragus. Loxia. Linota. Emberiza. STURNIDÆ. Sturnus. ALAUDIDÆ. Otocorys. PICIDÆ. Picoides. Picus. Hyopicus. Dryocopus. YUNGIDÆ. Yunx. PTEROCLIDÆ. Syrrhaptes. TETRAONIDÆ. Tetrao. Tetraogallus. Lerwa. Lagopus. VULTURIDÆ. Gypaëtus. Vultur. FALCONIDÆ. Archibuteo. ORIENTAL GENERA. SYLVIIDÆ. Suya. Calliope. Larvivora. Tribura. Horites. Abrornis. Copsychus. TURDIDÆ. Oreocincla. TIMALIIDÆ. Alcippe. Timalia. Pterocyclus. Garrulax. Trochalopteron. Pomatorhinus. {225} Suthora. PANURIDÆ. Paradoxornis. CINCLIDÆ. Enicurus. Myiophonus. TROGLODYTIDÆ. Pnoepyga. LIOTRICHIDÆ. Liothrix. Yuhina. Pteruthius. PYCNONOTIDÆ. Microscelis. Pycnonotus. Hypsipetes. CAMPEPHAGIDÆ. Pericrocotus. DICRURIDÆ. Dicrurus. Chibia. Buchanga. MUSCICAPIDÆ. Xanthopygia. Niltava. Tchitrea. CORVIDÆ. Urocissa. NECTARINEIDÆ. Æthopyga. MOTACILLIDÆ. Nemoricola. DICÆIDÆ. Zosterops. FRINGILLIDÆ. Melophus. Pyrgilauda. PLOCEIDÆ. Munia. STURNIDÆ. Acridotheres. Sturnia. PITTIDÆ. Pitta. PICIDÆ. Vivia. Yungipicus. Gecinus. CORACIIDÆ. Eurystomus. ALCEDINIDÆ. Halcyon. Ceryle. UPUPIDÆ. Upupa. PSITTACIDÆ. Palæornis. COLUMBIDÆ. Treron. Ianthænas. Macropygia. PHASIANIDÆ. Phasianus. Ceriornis. STRIGIDÆ. Scops. In the above lists there are rather more Oriental than Palæarctic genera; but it must be remembered that most of the former are summer migrants only, or stragglers just entering the sub-region; whereas the great majority of the latter are permanent residents, and a large proportion of them range over the greater part of the Manchurian district. Many of those in the Oriental column should perhaps be omitted, as we have no exact determination of their range, and the limits of the regions are very uncertain. It must be remembered, too, that the Palæarctic genera of Sylviidæ, Paridæ, and Fringillidæ, are often represented by numerous species, whereas the corresponding Oriental genera have for the most part only single species; and we shall then find that, except towards the borders of the Oriental region the Palæarctic element is strongly predominant. Four of the more especially Oriental groups are confined to Japan, the southern {226}extremity of which should perhaps come in the Oriental region. The great richness of this sub-region compared with that of Siberia is well shown by the fact, that a list of all the known land-birds of East Siberia, including Dahuria and the comparatively fertile Amoor Valley, contains only 190 species; whereas Père David's catalogue of the birds of Northern China with adjacent parts of East Thibet and Mongolia (a very much smaller area) contains for the same families 366 species. Of the Siberian birds more than 50 per cent, are European species, while those of the Manchurian sub-region comprise about half that proportion of land-birds which are identical with those of Europe. Japan is no doubt very imperfectly known, as only 134 land-birds are recorded from it. Of these twenty-two are peculiar species, a number that would probably be diminished were the Corea to be explored. Of the genera, only nine are Indo-Malayan, while forty-three are Palæarctic. _Plate III.--Scene on the Borders of North-West China and Mongolia with Characteristic Mammalia and Birds._--The mountainous districts of Northern China, with the adjacent portions of Thibet and Mongolia, are the head-quarters of the pheasant tribe, many of the most beautiful and remarkable species being found there only. In the north-western provinces of China and the southern parts of Mongolia may be found the species figured. That in the foreground is the superb golden pheasant (_Thaumalea picta_), a bird that can hardly be surpassed for splendour of plumage by any denizen of the tropics. The large bird perched above is the eared pheasant (_Crossoptilon auritum_), a species of comparatively sober plumage but of remarkable and elegant form. In the middle distance is Pallas's sand grouse (_Syrrhaptes paradoxus_), a curious bird, whose native country seems to be the high plains of Northern Asia, but which often abounds near Pekin, and in 1863 astonished European ornithologists by appearing in considerable numbers in Central and Western Europe, in every part of Great Britain, and even in Ireland. Plate III. [Illustration] CHARACTERISTIC ANIMALS OF NORTH CHINA. The quadruped figured is the curious racoon dog (_Nyctereutes procyonoides_), {227}an animal confined to North China, Japan, and the Amoor Valley, and having no close allies in any other part of the globe. In the distance are some deer, a group of animals very abundant and varied in this part of the Palæarctic region. _Reptiles and Amphibia._--Reptiles are scarce in North China, only four or five species of snakes, a lizard and one of the Geckotidæ occurring in the country round Pekin. The genus _Halys_ is the most characteristic form of snake, while _Callophis_, an oriental genus, extends to Japan. Among lizards, _Plestiodon_, _Maybouya_, _Tachydromus_, and _Gecko_ reach Japan, the two latter being very characteristic of the Oriental region. Amphibia are more abundant and interesting; _Hynobius_, _Onychodactylus_, and _Sieboldtia_ (Salamandridæ) being peculiar to it, while most of the European genera are also represented. _Fresh-water Fish._--Of these there are a few peculiar genera; as _Plecoglossus_ (Salmonidæ) from Japan; _Achilognathus_, _Pseudoperilampus_, _Ochetobius_, and _Opsariichthys_ (Cyprinidæ); and there are many other Chinese Cyprinidæ belonging to the border land of the Palæarctic and Oriental regions. _Insects._--The butterflies of this sub-region exhibit the same mixture of tropical and temperate forms as the birds. Most of the common European genera are represented, and there are species of _Parnassius_ in Japan and the Amoor. _Isodema_, a peculiar genus of Nymphalidæ is found near Ningpo, just within our limits; and _Sericinus_, one of the most beautiful genera of Papilionidæ is peculiar to North China, where four species occur, thus balancing the _Thais_ and _Doritis_ of Europe. The genus _Zephyrus_ (Lycænidæ) is well represented by six species in Japan and the Amoor, against two in Europe. _Papilio paris_ and _P. bianor_, magnificent insects of wholly tropical appearance, abound near Pekin, and allied forms inhabit Japan and the Amoor, as well as _P. demetrius_ and _P. alcinous_ belonging to the "Protenor" group of the Himalayas. Other tropical genera occurring in Japan, the Amoor, or North China are, _Debis_, _Neope_, _Mycalesis_, _Ypthimia_ (Satyridæ); _Thaumantis_ (Morphidæ), at Shanghae; _Euripus_, _Neptis_, _Athyma_ (Nymphalidæ); _Terias_ (Pieridæ); and the above-mentioned Papilionidæ. {228}_Coleoptera._--The beetles of Japan decidedly exhibit a mixture of tropical forms with others truly Palæarctic, and it has been with some naturalists a matter of doubt whether the southern and best known portion of the islands should not be joined to the Oriental region. An important addition to our knowledge of the insects of this country has recently been made by Mr. George Lewis, and a portion of his collections have been described by various entomologists in the _Transactions of the Entomological Society of London_. As the question is one of considerable interest we shall give a summary of the results fairly deducible from what is now known of the entomology of Japan; and it must be remembered that almost all our collections come from the southern districts, in what is almost a sub-tropical climate; so that if we find a considerable proportion of Palæarctic forms, we may be pretty sure that the preponderance will be much greater a little further north. Of Carabidæ Mr. Bates enumerates 244 species belonging to 84 genera, and by comparing these with the Coleoptera of a tract of about equal extent in western Europe, he concludes that there is little similarity, and that the cases of affinity to the forms of eastern tropical Asia preponderate. By comparing his genera with the distributions as given in _Gemminger and Harold's Catalogue_, a somewhat different result is arrived at. Leaving out the generic types altogether peculiar to Japan, and also those genera of such world-wide distribution that they afford no clear indications for our purpose, it appears that no less than twenty-two genera, containing seventy-four of the Japanese species, are either exclusively Palæarctic, Palæarctic and Nearctic, or highly characteristic of the Palæarctic region; then come thirteen genera containing eighty-seven of the species which have a very wide distribution, but are also Palæarctic: we next have seventeen genera containing twenty-four of the Japanese species which are decidedly Oriental and tropical. Here then the fair comparison is between the twenty-two genera and seventy-four species whose affinities are clearly Palæarctic or at least north temperate, and seventeen genera with twenty-four species which are Asiatic and tropical; and this seems to prove that, although South {229}Japan (like North China) has a considerable infusion of tropical forms, there is a preponderating substratum of Palæarctic forms, which clearly indicate the true position of the islands in zoological geography. There are also a few cases of what may be called eccentric distribution; which show that Japan, like many other island-groups, has served as a kind of refuge in which dying-out forms continue to maintain themselves. These, which are worthy of notice, are as follows: _Orthotrichus_ (1 sp.) has the only other species in Egypt; _Trechichus_ (1 sp.) has two other species, of which one inhabits Madeira, the other the Southern United States; _Perileptus_ (1 sp.) has two other species, of which one inhabits Bourbon, the other West Europe; and lastly, _Crepidogaster_ (1 sp.) has the other known species in South Africa. These cases diminish the value of the indications afforded by some of the Japanese forms, whose only allies are single species in various remote parts of the Oriental region. The Staphylinidæ have been described by Dr. Sharp, and his list exhibits a great preponderance of north temperate, or cosmopolitan forms, with a few which are decidedly tropical. The Pselaphidæ and Scydmenidæ, also described by Dr. Sharp, exhibit, according to that gentleman, "even a greater resemblance to those of North America than to those of Europe," but he says nothing of any tropical affinities. The water-beetles are all either Palæarctic or of wide distribution. The Lucanidæ (_Gemm. and Har. Cat._, 1868) exhibit an intermingling of Palæarctic and Oriental genera. The Cetoniidæ (_Gemm. and Har. Cat._, 1869) show, for North China and Japan, three Oriental to two Palæarctic genera. The Buprestidæ collected by Mr. Lewis have been described by Mr. Edward Saunders in the _Journal of the Linnæan Society_, vol. xi. p. 509. The collection consisted of thirty-six species belonging to fourteen genera. No less than thirteen of these are known also from India and the Malay Islands; nine from Europe; seven from Africa; six from America, and four from China. In six of the genera the Japanese species are said to be allied to those of the Oriental region; while in three they are allied to European forms, and in two to American. Considering {230}the southern latitude and warm climate in which these insects were mostly collected, and the proximity to Formosa and the Malay Islands compared with the enormous distance from Europe, this shows as much Palæarctic affinity as can be expected. In the Palæarctic region the group is only plentiful in the southern parts of Europe, which is cut off by the cold plateau of Thibet from all direct communication with Japan; while in the Oriental region it everywhere abounds and is, in fact, one of the most conspicuous and dominant families of Coleoptera. The Longicorns collected by Mr. Lewis have been described by Mr. Bates in the _Annals of Natural History for 1873_. The number of species now known from Japan is 107, belonging to sixty-four genera. The most important genera are _Leptura_, _Clytanthus_, _Monohammus_, _Praonetha_, _Exocentrus_, _Glenea_, and _Oberea_. There are twenty-one tropical genera, and seven peculiar to Japan, leaving thirty-six either Palæarctic or of very wide range. A number of the genera are Oriental and Malayan, and many characteristic European genera seem to be absent; but it is certain that not half the Japanese Longicorns are yet known, and many of these gaps will doubtless be filled up when the more northern islands are explored. The Phytophaga, described by Mr. Baly, appear to have a considerable preponderance of tropical Oriental forms. A considerable collection of Hymenoptera formed by Mr. Lewis have been described by Mr. Frederick Smith; and exhibit the interesting result, that while the bees and wasps are decidedly of tropical and Oriental forms, the Tenthredinidæ and Ichneumonidæ are as decidedly Palæarctic, "the general aspect of the collection being that of a European one, only a single exotic form being found among them." _Remarks on the General Character of the Fauna of Japan._--From a general view of the phenomena of distribution we feel justified in placing Japan in the Palæarctic region; although some tropical groups, especially of reptiles and insects, have largely occupied its southern portions; and these same groups have in many cases spread into Northern China, beyond the {231}usual dividing line of the Palæarctic and Oriental regions. The causes of such a phenomenon are not difficult to conceive. Even now, that portion of the Palæarctic region between Western Asia and Japan is, for the most part, a bleak and inhospitable region, abounding in desert plateaus, and with a rigorous climate even in its most favoured districts, and can, therefore, support but a scanty population of snakes, and of such groups of insects as require flowers, forests, or a considerable period of warm summer weather; and it is precisely these which are represented in Japan and North China by tropical forms. We must also consider, that during the Glacial epoch this whole region would have become still less productive, and that, as the southern limit of the ice retired northward, it would be followed up by many tropical forms along with such as had been driven south by its advance, and had survived to return to their northern homes. It is also evident that Japan has a more equable and probably moister climate than the opposite shores of China, and has also a very different geological character, being rocky and broken, often volcanic, and supporting a rich, varied, and peculiar vegetation. It would thus be well adapted to support all the more hardy denizens of the tropics which might at various times reach it, while it might not be so well adapted for the more boreal forms from Mongolia or Siberia. The fact that a mixture of such forms occurs there, is then, little to be wondered at, but we may rather marvel that they are not more predominant, and that even in the extreme south, the most abundant forms of mammal, bird, and insect, are modifications of familiar Palæarctic types. The fact clearly indicates that the former land connections of Japan with the continent have been in a northerly rather than in a southerly direction, and that the tropical immigrants have had difficulties to contend with, and have found the land already fairly stocked with northern aborigines in almost every class and order of animals. _General Conclusions as to the Fauna of the Palæarctic Region._--From the account that has now been given of the fauna {232}of the Palæarctic region, it is evident that it owes many of its deficiencies and some of its peculiarities to the influence of the Glacial epoch, combined with those important changes of physical geography which accompanied or preceded it. The elevation of the old Sarahan sea and the complete formation of the Mediterranean, are the most important of these changes in the western portion of the region. In the centre, a wide arm of the Arctic Ocean extended southward from the Gulf of Obi to the Aral and the Caspian, dividing northern Europe and Asia. At this time our European and Siberian sub-regions were probably more distinct than they are now, their complete fusion having been effected since the Glacial epoch. As we know that the Himalayas have greatly increased in altitude during the Tertiary period, it is not impossible that during the Miocene and Pliocene epochs the vast plateau of Central Asia was much less elevated and less completely cut off from the influence of rain-bearing winds. It might then have been far more fertile, and have supported a rich and varied animal population, a few relics of which we see in the Thibetan antelopes, yaks, and wild horses. The influence of yet earlier changes of physical geography, and the relations of the Palæarctic to the tropical regions immediately south of it, will be better understood when we have examined and discussed the faunas of the Ethiopian and Oriental regions. {233}TABLES OF DISTRIBUTION. In constructing these tables showing the distribution of various classes of animals in the Palæarctic region, the following sources of information have been chiefly relied on, in addition to the general treatises, monographs, and catalogues used in compiling the fourth part of this work. _Mammalia._--Lord Clement's Mammalia and Reptiles of Europe; Siebold's Fauna Japonica; Père David's List of Mammalia of North China and Thibet; Swinhoe's Chinese Mammalia; Radde's List of Mammalia of South-Eastern Siberia; Canon Tristram's Lists for Sahara and Palestine; Papers by Professor Milne-Edwards, Mr. Blanford, Mr. Sclater, and the local lists given by Mr. A. Murray in the Appendix to his Geographical Distribution of Mammalia. _Birds._--Blasius' List of Birds of Europe; Godman, On Birds of Azores, Madeira, and Canaries; Middendorf, for Siberia; Père David and Mr. Swinhoe, for China and Mongolia; Homeyer, for East Siberia; Mr. Blanford, for Persia and the high Himalayas; Mr. Elwes's paper on the Distribution of Asiatic Birds; Canon Tristram, for the Sahara and Palestine; Professor Newton, for Iceland and Greenland; Mr. Dresser, for Scandinavia; and numerous papers and notes in the Ibis; Journal für Ornithologie; Annals and Mag. of Nat. History; and Proceedings of the Zoological Society. _Reptiles and Amphibia._--Schreiber's European Herpetology. {234}TABLE I. _FAMILIES OF ANIMALS INHABITING THE PALÆARCTIC REGION._ EXPLANATION. Names in _italics_ show families peculiar to the region. Names inclosed thus (......) barely enter the region, and are not considered properly to belong to it. Numbers are not consecutive, but correspond to those in Part IV. ---------------------+-------------------+------------------------------- | Sub-regions | | 1=Europe. | Order and Family | 2=Mediterranean. | Range beyond the Region. | 3=Siberian. | | 4=Japan. | ---------------------+----+----+----+----+------------------------------- | 1. | 2. | 3. | 4. | ---------------------+----+----+----+----+------------------------------- | | | | | MAMMALIA. | | | | | PRIMATES. | | | | | 3. Cynopithecidæ | | -- | | -- |Ethiopian, Oriental | | | | | CHIROPTERA. | | | | | 9. (Pteropidæ) | | | | -- |Tropics of E. Hemisphere 11. Rhinolophidæ | -- | -- | -- | -- |Warmer parts of E. Hemis. 12. Vespertilionidæ | -- | -- | -- | -- |Cosmopolite 13. Noctilionidæ | | -- | | |Tropical regions | | | | | INSECTIVORA. | | | | | 15. Macroscelididæ | | -- | | |Ethiopian 17. Erinaceidæ | -- | -- | -- | -- |Oriental, S. Africa 21. Talpidæ | -- | -- | -- | -- |Nearctic, Oriental 22. Soricidæ | -- | -- | -- | -- |Cosmopolite, excl. Australia | | | | | and S. America | | | | | CARNIVORA. | | | | | 23. Felidæ | -- | -- | -- | -- |All regions but Australian 25. Viverridæ | | -- | | |Ethiopian, Oriental 27. Hyænidæ | | -- | | |Ethiopian, Oriental 28. Canidæ | -- | -- | -- | -- |All regions but Australian 29. Mustelidæ | -- | -- | -- | -- |All regions but Australian 31. Æluridæ | | | | -- |Oriental 32. Ursidæ | -- | -- | -- | -- |Nearctic, Oriental, Andes 33. Otariidæ | | | | -- |N. and S. temperate zones 34. Trichechidæ | -- | | -- | |Arctic regions 35. Phocidæ | -- | -- | -- | -- |N. and S. temperate zones | | | | | CETACEA. | | | | | 36 to 41. | | | | |Oceanic | | | | | SIRENIA. | | | | | 42. Manatidæ | -- | | -- | |Tropics, from Brazil to | | | | | N. Australia | | | | | UNGULATA. | | | | | 43. Equidæ | | -- | -- | |Ethiopian 47. Suidæ | -- | -- | -- | -- |Cosmopolite, excl. Nearctic | | | | | reg. and Australia 48. Camelidæ | | -- | -- | |Andes 50. Cervidæ | -- | -- | -- | -- |All regions but Ethiopian and | | | | | Australian 52. Bovidæ | -- | -- | -- | -- |All regions but Neotropical and | | | | | Australian | | | | | HYRACOIDÆ. | | | | | 54. (Hyracidæ) | | -- | | |Ethiopian family | | | | | RODENTIA. | | | | | 55. Muridæ | -- | -- | -- | -- |Almost Cosmopolite 56. Spalacidæ | -- | -- | -- | |Ethiopian, Oriental 57. Dipodidæ | | -- | -- | -- |Ethiopian, Nearctic 58. Myoxidæ | -- | -- | -- | -- |Ethiopian 60. Castoridæ | -- | | -- | |Nearctic 61. Sciuridæ | -- | -- | -- | -- |All regions but Australian 64. Octodontidæ | | -- | | |Abyssinia, Neotropical 67. Hystricidæ | | -- | | |Ethiopian, Oriental 69. Lagomyidæ | | | -- | |Nearctic 70. Leporidæ | -- | -- | -- | -- |All regions but Australian | | | | | BIRDS. | | | | | PASSERES. | -- | -- | -- | -- | 1. Turdidæ | -- | -- | -- | -- |Cosmopolite 2. Sylviidæ | | -- | | -- |Cosmopolite 3. Timaliidæ | -- | -- | -- | -- |Ethiopian, Oriental, Australian 4. Panuridæ | -- | -- | -- | -- |Nearctic, Oriental 5. Cinclidæ | -- | -- | -- | -- |Oriental 6. Troglodytidæ | -- | -- | -- | -- |American, Oriental 8. Certhiidæ | -- | -- | -- | -- |Oriental, Nearctic 9. Sittidæ | -- | -- | -- | -- |Nearctic, Oriental, Australian, | | | | | Madagascar 10. Paridæ | -- | -- | | -- |Nearctic, Oriental, Australian | | | | | [?] 13. Pycnonotidæ | | -- | | -- |Oriental, Ethiopian 14. Oriolidæ | -- | -- | -- | -- |Ethiopian, Oriental, Australian 17. Muscicapidæ | | | | |Eastern Hemisphere 19. Laniidæ | -- | -- | -- | -- |Eastern Hemisphere and N. | | | | | America 20. Corvidæ | -- | -- | -- | -- |Cosmopolite 23. (Nectariniidæ) | | -- | | |Ethiopian, Oriental, Australian 24. (Dicæidæ) | | | | -- |Ethiopian, Oriental, Australian 29. Ampelidæ | -- | -- | -- | -- |Nearctic 30. Hirundinidæ | -- | -- | -- | -- |Cosmopolite 33. Fringillidæ | -- | -- | -- | -- |All regions but Australian 35. Sturnidæ | -- | -- | -- | -- |Eastern Hemisphere 37. Alaudidæ | -- | -- | -- | -- |All regions but Neotropical 38. Motacillidæ | -- | -- | -- | -- |Cosmopolite 47. (Pittidæ) | | | | -- |Oriental, Australian, Ethiopian | | | | | PICARIÆ. | | | | | 51. Picidæ | -- | -- | -- | -- |All regions but Australian 52. Yungidæ | -- | -- | -- | -- |N. W. India, N. E. Africa, | | | | | S. Africa 58. Cuculidæ | -- | -- | -- | -- |Almost Cosmopolite 62. Coraciidæ | -- | -- | -- | -- |Ethiopian, Oriental, Australian 63. Meropidæ | -- | -- | | |Ethiopian, Oriental, Australian 67. Alcedinidæ | -- | -- | -- | -- |Cosmopolite 69. Upupidæ | | -- | | -- |Ethiopian, Oriental 73. Caprimulgidæ | -- | -- | -- | -- |Cosmopolite 74. Cypselidæ | -- | -- | -- | -- |Almost Cosmopolite | | | | | COLUMBÆ. | | | | | 84. Columbidæ | -- | -- | -- | -- |Cosmopolite | | | | | GALLINÆ. | | | | | 86. Pteroclidæ | -- | -- | -- | -- |Ethiopian, Indian 87. Tetraonidæ | -- | -- | -- | -- |Nearctic, Ethiopian, Oriental 88. Phasianidæ | | -- | -- | -- |Oriental, Ethiopian, Nearctic 89. Turnicidæ | | -- | | -- |Ethiopian, Oriental, Australian | | | | | ACCIPITRES. | | | | | 94. Vulturidæ | -- | -- | -- | -- |All regions but Australian 96. Falconidæ | -- | -- | -- | -- |Cosmopolite 97. Pandionidæ | -- | -- | -- | -- |Cosmopolite 98. Strigidæ | -- | -- | -- | -- |Cosmopolite | | | | | GRALLÆ. | | | | | 99. Rallidæ | -- | -- | -- | -- |Cosmopolite 100. Scolopacidæ | -- | -- | -- | -- |Cosmopolite 104. Glareolidæ | -- | -- | -- | -- |Ethiopian, Oriental, Australian 105. Charadriidæ | -- | -- | -- | -- |Cosmopolite 106. Otididæ | -- | -- | -- | -- |Ethiopian, Oriental, Australian 107. Gruidæ | -- | -- | -- | -- |Eastern Hemisphere, and | | | | | N. America 113. Ardeidæ | -- | -- | -- | -- |Cosmopolite 114. Plataleidæ | -- | -- | -- | -- |Almost Cosmopolite 115. Ciconiidæ | -- | -- | -- | -- |Nearly Cosmopolite 117. Phænicopteridæ | | -- | | |Neotropical, Ethiopian, Indian | | | | | ANSERES. | | | | | 118. Anatidæ | -- | -- | -- | -- |Cosmopolite 119. Laridæ | -- | -- | -- | -- |Cosmopolite 120. Procellariidæ | -- | -- | -- | -- |Cosmopolite 121. Pelecanidæ | -- | -- | -- | -- |Cosmopolite 123. Colymbidæ | -- | | -- | -- |Arctic and N. Temperate 124. Podicipidæ | -- | -- | -- | -- |Cosmopolite 125. Alcidæ | -- | | -- | -- |N. Temperate zone | | | | | REPTILIA. | | | | | OPHIDIA. | | | | | 1. Typhlopidæ | | -- | | -- |All regions but Nearctic 5. Calamariidæ | | -- | | |All other regions 6. Oligodontidæ | | | | -- |Oriental and Neotropical 7. Colubridæ | -- | -- | -- | -- |Almost Cosmopolite 8. Homalopsidæ | | -- | -- | -- |Oriental, and all other regions 9. Psammophidæ | | -- | | |Ethiopian and Oriental 18. Erycidæ | | -- | | |Oriental and Ethiopian 20. Elapidæ | | | | -- |Australian and all other | | | | | regions 24. Crotalidæ | | | -- | -- |Nearctic, Neotropical, Oriental 25. Viperidæ | -- | -- | -- | -- |Ethiopian, Oriental | | | | | LACERTILIA. | | | | | 26. _Trogonophidæ_ | | -- | | | 28. Amphisbænidæ | | -- | | |Ethiopian, Neotropical 30. Varanidæ | | -- | | |Oriental, Ethiopian, Australian 33. Lacertidæ | -- | -- | -- | -- |All continents but American 34. Zonuridæ | | -- | | |America, Africa, N. India 41. Gymnopthalmidæ | -- | -- | -- | |Ethiopian, Australian, | | | | | Neotropical 45. Scincidæ | -- | -- | -- | -- |Almost Cosmopolite 46. _Ophiomoridæ_ | | -- | | | 47. Sepidæ | | -- | | |Ethiopian 49. Geckotidæ | | -- | -- | -- |Almost Cosmopolite 51. Agamidæ | | -- | -- | -- |All continents but America 52. Chamæleonidæ | | -- | | |Ethiopian, Oriental | | | | | CHELONIA. | | | | | 57. Testudinidæ | -- | -- | | -- |All continents but Australia 59. Trionychidæ | | | | -- |Ethiopian, Oriental, Nearctic 60. Cheloniidæ | | | | |Marine | | | | | AMPHIBIA. | | | | | URODELA. | | | | | 3. Proteidæ | -- | | | |Nearctic 5. Menopomidæ | | | | -- |Nearctic 6. Salamandridæ | -- | -- | -- | -- |Nearctic to Andes of Bogota | | | | | ANOURA. | | | | | 10. Bufonidæ | -- | -- | -- | -- |All continents but Australia 13. Bombinatoridæ | -- | -- | | |Neotropical, New Zealand 15. Alytidæ | -- | | | |All regions but Oriental 17. Hylidæ | -- | -- | -- | |All regions but Ethiopian 18. Polypedatidæ | | | -- | -- |All the regions 19. Ranidæ | -- | -- | -- | -- |Almost Cosmopolite 20. Discoglossidæ | -- | -- | -- | -- |All regions but Nearctic | | | | | FISHES (FRESH-WATER).| | | | | ACANTHOPTERYGII. | | | | | 1. Gasterosteidæ | -- | -- | -- | -- |Nearctic 3. Percidæ | -- | -- | -- | -- |All regions but Australian 12. Scienidæ | -- | -- | | -- |All regions but Australian 26. _Comephoridæ_ | | | -- | | 37. Atherinidæ | -- | -- | | |N. America and Australia | | | | | PHYSOSTOMI. | | | | | 59. Siluridæ | -- | -- | -- | -- |All warm regions 65. Salmonidæ | -- | -- | -- | -- |Nearctic, New Zealand 70. Esocidæ | -- | -- | | |Nearctic 71. Umbridæ | -- | | | |Nearctic 73. Cyprinodontidæ | | -- | | |All regions but Australia 75. Cyprinidæ | -- | -- | -- | -- |All regions but Australian and | | | | | Neotropical | | | | | GANOIDEI. | | | | | 96. Accipenseridæ | -- | -- | -- | |Nearctic 97. Polydontidæ | | | | -- |Nearctic | | | | | INSECTS. | | | | | LEPIDOPTERA (PART). | | | | | DURINI (BUTTERFLIES).| | | | | 1. Danaidæ | -- | -- | | -- |All tropical regions 2. Satyridæ | -- | -- | -- | -- |Cosmopolite 8. Nymphalidæ | -- | -- | -- | -- |Cosmopolite 9. Libytheidæ | -- | -- | | |All continents but Australia 10. Nemeobeidæ | -- | | | |Absent from Nearctic region and | | | | | Australia 13. Lycænidæ | -- | -- | -- | -- |Cosmopolite 14. Pieridæ | -- | -- | -- | -- |Cosmopolite 15. Papilionidæ | -- | -- | -- | -- |Cosmopolite 16. Hesperidæ | -- | -- | -- | -- |Cosmopolite | | | | | SPHINGIDEA. | | | | | 17. Zygænidæ | -- | -- | -- | -- |Cosmopolite 21. Stygiidæ | -- | -- | -- | -- |Neotropical 22. Ægeriidæ | -- | -- | -- | -- |Absent only from Australia 23. Sphingidæ | -- | -- | -- | -- |Cosmopolite ---------------------+----+----+----+----+------------------------------- COLEOPTERA.--Of about 80 families into which the Coleoptera are divided, all the more important are cosmopolite, or nearly so. It would therefore unnecessarily occupy space to give tables of the whole for each region. LAND SHELLS.--The more important families being cosmopolite, and the smaller ones being somewhat uncertain in their limits, the reader is referred to the account of the families and genera under each region, and to the chapter on Mollusca in the concluding part of this work, for such information as can be given of their distribution. {239}TABLE II. _LIST OF THE GENERA OF TERRESTIAL MAMMALIA AND BIRDS INHABITING THE PALÆARCTIC REGION._ EXPLANATION. Names in _italics_ show genera peculiar to the region. Names inclosed thus (...) show genera which just enter the region, but are not considered properly to belong to it. Genera which undoubtedly belong to the region are numbered consecutively. _MAMMALIA._ -------------------+-------+----------------------+---------------------- Order, Family, and | No. of| Range within | Range beyond Genus. |Species| the Region. | the Region. -------------------+-------+----------------------+---------------------- | | | PRIMATES. | | | SEMNOPITHECIDÆ. | | | | | | (Semnopithecus | 1 |Eastern Thibet) |Oriental genus | | | CYNOPITHECIDÆ. | | | | | | 1. Macacus | 4 |Gibraltar, N. Africa, |Oriental | | E. Thibet to Japan | | | | CHIROPTERA. | | | PTEROPIDÆ. | | | | | | (Pteropus | 2 |Egypt, Japan) |Tropics of the E. . | | | Hemis (Xantharpyia | 1 |N. Africa, Palestine) |Oriental, Austro- | | | Malayan | | | RHINOLOPHIDÆ. | | | | | | 2. Rhinolphus | 9 |Temperate & Southern |Warmer parts E. | | parts of Region | Hemisphere (Asellia | 1 |Egypt) |Ethiopian, Java (_Rhinopoma_ | 1 |Egypt, Palestine) |[?] India (Nycteris | 1 |Egypt) |Nubia, Himalaya | | | VESPERTILIONIDÆ. | | | | | | 3. Vesperugo | 1 |Siberia, Amoorland |[?] 4. _Otonycteris_ | 1 |Egypt |[?] 5. Vespertilio | 35 |The whole region |Cosmopolite (Kerivoula | 1 |N. China) |Oriental, S. Africa 6. Miniopteris | 1 |S. Europe, N. Africa, |S. Afric. Malaya, | | Japan | Austral. 7. Plecotus | 1 |S. Europe |Himalayas 8. Barbastellus | 2 |Mid. and S. Europe, |Darjeeling, Timor | | Palestine | | | | NOCTILIONIDÆ. | | | | | | 9. Molossus | 2 |S. Europe, N. Africa |Ethiop., Neotrop., | | | Australian | | | INSECTIVORA. | | | ERINACEIDÆ. | | | | | | 10. Erinaceus | 4 |The whole region; excl.|Oriental, Africa. | | Japan | | | | TALPIDÆ. | | | | | | 11. _Talpa_ | 5 |The whole region |N. India 12. _Scaptochirus_ | 1 |N. China | 13. _Anurosorex_ | 1 |N. China | 14. _Scaptonyx_ | 1 |N. China | 15. _Myogale_ | 2 |S. E. Russia, Pyrenees | 16. _Nectogale_ | 1 |Thibet | 17. Urotrichus | 1 |Japan |N. W. America 18. _Uropsilus_ | 1 |E. Thibet | | | | SORICIDÆ. | | | | | | 19. Sorex | 10 |The whole region |Absent from Australia | | | & S. America 20. Crocidura | 4 |W. Europe to N. China | [?] | | | CARNIVORA. | | | FELIDÆ. | | | | | | 21. Felis | 12 |The whole region; excl.|All regions but | | extreme North | Austral. 22. Lyncus | 9 |S. Europe to Arctic sea|America N. of 66° N. | | | Lat. | | | VIVERRIDÆ. | | | | | | (Viverra | 1 |N. China) |Oriental and Ethiopian 23. Genetta | 1 |S. Europe & N. Africa, |Ethiopian | | Palestine | (Herpestes | 1 |N. Africa, Spain [?], |Oriental and Ethiopian | | Palestine) | | | | HYÆNIDÆ. | | | | | | 24. Hyæna | 1 |N. Africa and S. W. |Ethiopian, India | | Asia | | | | CANIDÆ. | | | | | | 25. Canis | 4 |The whole region |All reg. but Austral. | | | [?] 26. _Nyctereutes_ | 1 |Japan, Amoorland, N. | | | China | | | | MUSTELIDÆ. | | | | | | 27. Martes | 7 |N. Europe and Asia, E. |Oriental, Nearctic | | Thibet | 28. _Putorius_ | 3 |W. Europe to N. E. Asia| 29. Mustela | 10 |The whole region |Nearctic, Ethiop., | | | Himalayas, Peru 30. Vison | 2 |Europe and Siberia |N. America, N. India, | | | China 31. Gulo | 1 |The Arctic regions |Arctic America 32. Lutra | 2 |The whole region |Oriental 33. _Lutronectes_ | 1 |Japan | 34. Enhydris | 1 |N. Asia and Japan |California 35. _Meles_ | 2 |Cen. Europe, Palestine,|China to Hongkong | | N. China, Japan | | | | ÆLURIDÆ. | | | | | | 36. Ælurus | 1 |S. E. Thibet |Nepal 37. _Æluropus_ | 1 |E. Thibet | | | | URSIDÆ. | | | | | | 38. Thalassarctos | 1 |Arctic regions |Arctic America 39. Ursus | 4 |The whole region |Oriental, Nearctic, | | | Chili | | | OTARIIDÆ. | | | | | | 40. Callorhinus | 1 |Kamschatka and | | | Behring's Straits | 41. Zalophus | 1 |Japan |California 42. Eumetopias | 1 |Japan, Behring's |California | | Straits | | | | TRICHECHIDÆ. | | | | | | 43. Trichechus | 1 |Polar Seas |Arctic America | | | PHOCIDÆ. | | | | | | 44. Callocephalus | 3 |North Sea, Caspian, |Greenland | | Lake Baikal | 45. Pagomys | 2 |North Sea, Japan |N. Pacific 46. Pagophilus | 2 |Northern Seas |N. Pacific 47. Phoca | 2 |Northern Seas |N. Pacific 48. Halichærus | 1 |North Sea and Baltic |Greenland 49. _Pelagius_ | 2 |Madeira to Black Sea | 50. Cystophora | 2 |N. Atlantic |N. Atlantic | | | SIRENIA. | | |Tropics & Behring's | | | Strts. | | | CETACEA. | | |Oceanic | | | UNGULATA. | | | EQUIDÆ. | | | | | | 51. Equus | 4 |Cent. and W. Asia & N. |Ethiopian | | Africa | | | | SUIDÆ. | | | | | | 52. Sus | 2 |The whole region |Oriental, Austro- | | | Malayan | | | CAMELIDÆ. | | | | | | 53. _Camelus_ | 2 |Deserts of Cent. and W.| | | Asia and N. Africa | | | | CERVIDÆ. | | | | | | 54. Alces | 1 |North Europe and Asia |N. America 55. Tarandus | 1 |Arctic Europe and Asia |Arctic America 56. Cervus | 8 |The whole region |All regions but | | | Austral. 57. _Dama_ | 1 |Mediterranean district | 58. _Elaphodus_ | 1 |N. W. China | 59. _Lophotragus_ | 1 |N. China | 60. _Capreolus_ | 2 |Temp. Europe and W. | | | Asia and N. China | 61. _Moschus_ | 1 |Amoor R., N. China, to | | | Himalayas | 62. _Hydropotes_ | 1 |N. China | | | | BOVIDÆ. | | | | | | 63. { Bos | 1 |Europe, (not wild) |Oriental 64. { Bison | 1 |Poland and Caucasus |Nearctic 65. { _Poephagus_ | 1 |Thibet | 66. _Addax_ | 1 |N. Africa to Syria | 67. Oryx | 1 |N. Africa to Syria |Ethiopian deserts 68. { Gazella | 12 |N. Africa to Persia, |S. Africa, India { | | and Beloochistan | 69. { _Procapra_ | 2 |W. Thibet and Mongolia | 70. {_Saiga_ | 1 |E. Europe and W. Asia | 71. {_Pantholops_ | 1 |W. Thibet | (Alcephalus | 1 |Syria) |Ethiopian genus. 72. _Budorcas_ | 2 |E. Himalayas to E. | | | Thibet | 73. _Rupicapra_ | 2 |Pyrenees to Caucasus | 74. Nemorhedus | 7 |E. Himalayas to E. |Oriental to Sumatra, | | China and Japan | Formosa 75. Capra | 20 |Spain to Thibet and |Nilgherries, Rocky | | N.E. Africa | Mtns. | | | HYRACOIDEA. | | | HYRACIDÆ. | | | | | | (Hyrax | 1 |Syria) |Ethiopian genus | | | RODENTIA. | | | MURIDÆ. | | | | | | 76. Mus |?15 |The whole region |E. Hemisphere 77. _Cricetus_ | 9 |The whole region | 78. _Cricetulus_ | 3 |N. China | 79. Meriones | 8 |W. and Central Asia to |Ethiopian, Indian. | | N. China, N. Africa | 80. _Rhombomys_ | 6 |E. Europe, Cent. Asia, | | | N. Africa | 81. _Psammomys_ | 3 |Egypt and Palestine | 82. _Sminthus_ | 3 |East Europe, Siberia | 83. Arvicola |?21 |The whole region |Himalayas, Nearctic 84. Cuniculus | 1 |N. E. Europe, Siberia |Arctic America 85. Myodes | 1 |North of region |Nearctic 86. _Myospalax_ | 3 |Altai Mountains and N. | | | China | | | | SPALACIDÆ. | | | | | | 87. _Ellobius_ | 1 |S. Russia and S. W. | | | Siberia | 88. _Spalax_ | 1 |Hungary and Greece to | | | W. Asia, Palestine | | | | DIPODIDÆ. | | | | | | 89. Dipus |?15 |S. E. Europe and N. |Africa, India | | Africa to N. China | | | | MYOXIDÆ. | | | | | | 90. Myoxus | 12 |Temperate parts of |Ethiopian | | whole region | | | | CASTORIDÆ. | | | | | | 91. Castor | 1 |Temperate zone, from |N. America | | France to Amoorland | | | | SCIURIDÆ. | | | | | | 92. Sciurus | 8 |The whole region |All regions but | | | Austral. 92a. Tamias | 1 |All Northern Asia |N. America 93. Sciuropterus | 4 |Finland to Siberia and |Oriental, Nearctic | | Japan | 94. Pteromys | 3 |Japan and W. China |Oriental 95. Spermophilus | 10 |E. Europe to N. China |Nearctic | | and Kamschatka | 96. Arctomys. | 4 |Alps to E. Thibet and |Nearctic | | Kamschatka | | | | OCTODONTIDÆ. | | | | | | 97._Ctenodactylus_ | 1 |N. Africa | | | | HYSTRICIDÆ. | | | | | | 98. Hystrix | 2 |S. Europe, Palestine, |Ethiopian, Oriental | | N. China. | | | | LAGOMYIDÆ. | | | | | | 99. Lagomys | 10 |Volga to E. Thibet and |Nearctic | | Kamschatka | | | | LEPORIDÆ. | | | | | | 100. Lepus | 12 |The whole region |All regions but | | | Austral. _BIRDS._ PASSERES. | | | TURDIDÆ. | | | | | | 1. Turdus | 18 |The whole region |Almost cosmopolite | |(excluding Spitsbergen)| 2. Oreocincla | 1 |N. E. Asia and Japan, |Oriental and | | straggler to Europe | Australian 3. Monticola | 3 |S. Europe, N. Africa, |Oriental and | | Palestine, N. China | S. African (Bessornis | 1 |Palestine) |Tropical and | | | S. Africa | | | SYLVIIDÆ. | | | | | | 4. Cisticola | 1 |S. W. Europe, N. |Ethiop., Orient., | | Africa, Japan | Austral. 5. {Acrocephalus | 10 |W. Europe to Japan |Orient., Ethiop., { | | | Austral. 6. {_Dumeticola_ | 4 |Nepaul, Lake Baikal, | { | | E. Thibet high | 7. {_Potamodus_ | 3 |W. and S. Europe, | { | | N. Africa, E. Thibet | 8. {_Lusciniola_ | 1 |S. Europe | 9. {_Locustella_ | 7 |W. Europe and N. Africa|India, winter { | | to Japan | migrants(?) 10. {Bradyptetus | 2 |S. Europe and Palestine|E. and S. Africa 11. {_Calamodus_ | ?3 |Europe, N. Africa, | | | Palestine | 12. {Phylloscopus | 6 |The whole region |Oriental { | | (excluding western | { | | islands) | 13. {Hypolais | 9 |Europe, N. Africa, |China, Moluccas, { | | Palestine, China | India, Africa 14. {Abrornis | 2 |Cashmere, E. Thibet |Oriental region 15. {Reguloides | 2 |Europe and China |N. India, Formosa 16. {Regulus | 4 |The whole region |N. and Central America | | (excluding Iceland, | | | &c.) | 17. {Aedon | 2 |S. Europe, W. Asia, |E. and S. Africa { | | N. Africa | 18. {_Pyrophthalma_ | 2 |E. Europe and Palestine| 19. {_Melizophilus_ | 2 |W. and S. Europe, | { | | Sardinia | 20. {_Sylvia_ | 6 |Madeira to W. India, |N. E. Africa, Ceylon { | | N. Africa | migrants(?) 21. {_Curruca_ | 7 |Madeira to India, |E. Africa, India, | | N. Africa | migrants 22. {_Luscinia_ | 2 |W. Europe, N. Africa, | { | | Persia | 23. {_Cyanecula_ | 3 |Europe and N. Africa to|Abyssinia and India { | | Kamschatka | migrants 24. {_Calliope_ | 2 |N. Asia, Himalayas, |Centl. India { | | China | (? migrant) 25. {_Erithacus_ | 3 |Atlantic Islands to | { | | Japan | 26. {_Grandala_ | 1 |High Himalayas and | | | E. Thibet | 27. { Ruticilla | 10 |Eu. to Japan, N. Afr., |Abyssinia, India { | | Himalayas | 28. { Larvivora | 2 |E. Thibet, Amoor, Japan|Oriental 29. Dromolæa | 3 |S. Europe, N. Africa, |Ethiopian | | Palestine | 30. Saxicola | 10 |The whole region |E. and S. Africa, | | | India 31. Cercomela | 2 |Palestine (a desert |N. E. Africa, N. W. | | genus) | India 32. Pratincola | 3 |W. Europe, N. Africa to|Ethiopian to Oriental | | India | 33. _Accentor_ | 12 |W. Europe to Japan; |Himalayas(?) in winter | | high Himalayas | | | | TIMALIIDÆ. | | | | | | 34. _Pterorhinus_ | 3 |Thibet and N. W. China | (Malacocercus | 1 |Palestine) |Oriental genus (Crateropus | 2 |N. Africa, Persia) |Ethiopian genus (Trochalopteron | 3 |E. Thibet) |Oriental genus (Ianthocincla | 3 |E. Thibet) |Oriental genus | | | PANURIDÆ. | | | | | | (Paradoxornis | 3 |Himalayas and |(?)Oriental genus | | E. Thibet) | 35. _Conostoma_ | 1 |High Himalayas | | | E. Thibet) | 36. Suthora | 3 |E. Thibet |Himalayas, China, | | | Formosa 37. _Panurus_ | 1 |W. Europe to W. Siberia| 38. _Heteromorpha_ | 1 |Nepaul and E. Thibet, | | | from 10,000 feet | | | altitude | 39. _Cholornis_ | 1 |E. Thibet | | | | CINCLIDÆ. | | | | | | 40. Cinclus | 5 |The whole region |American highlands | | (Atlantic Islands | | | excluded) | (Myiophonus | 1 |Turkestan, Thian-Shan |Oriental genus | | Mountains, 6,000 feet| | | | TROGLODYTIDÆ. | | | | | | 41. Troglodytes | 3 |Iceland and Britain to |Neotropical and | | Japan | Nearctic, Himalayas (Pnoepyga | 2 |E. Thibet) |Oriental genus | | | CERTHIIDÆ. | | | | | | 42. Certhia | 2 |W. Europe to N. China |Himalayas, Nearctic 43. _Tichodroma_ | 1 |S. Europe to N. China |Abyssinia, Nepaul, | | | high | | | SITTIDÆ. | | | | | | 44. Sitta | 7 |W. Europe to Himalayas India, Nearctic | | and Japan | | | | PARIDÆ. | | | | | | 45. Parus | 20 |W. Europe to Kamschatka|Nearctic, Oriental, | | N. Africa | Ethiopian 46. Lophophanes | 6 |Europe and high |Nearctic | | Himalayas | 47. _Acredula_ | 6 |W. Europe to N. China | | | and Kamschatka | 48. Ægithalus | 1 |S. E. Europe |Ethiopian | | | LIOTRICHIDÆ. | | | | | | (Proparus | 4 |Moupin, in E. Thibet) |Oriental genus and | | | fam. | | | PYCNONOTIDÆ. | | | | | | 49. Microscelis | 1 |Japan |Oriental genus 50. Pycnonotus | 2 |Palestine, N. China, |Oriental and Ethiopian | | Japan | | | | ORIOLIDÆ. | | | | | | 51. Oriolus | |S. Europe, China |Ethiopian and Oriental | | | MUSCICAPIDÆ. | | | | | | 52. Muscicapa | 2 |W. and Central Europe |Ethiopian. 53. Butalis | 2 |W. Europe to Japan and |E. and S. Africa, | | China | Moluccas 54. Erythrosterna | 3 |Central Europe to N. |Oriental & Madagascar | | China and Japan | (Xanthopygia | 1 |Japan) |Oriental genus (Eumyias-- | 1 |E. Thibet) |Oriental genus (Cyanoptila | 1 |Japan and Amoor) |Oriental genus (Siphia | 1 |Moupin, E. Thibet) |Oriental genus 55. Tchitrea | 2 |N. China and Japan |Ethiopian and Oriental | | | LANIIDÆ. | | | | | | 56. Lanius | 11 |The whole region (excl.|Nearctic, Ethiopian, | | Atlantic Islands) | Oriental (Telephonus | 1 |N. Africa) |Ethiopian genus | | | CORVIDÆ. | | | | | | 57. Garrulus | 7 |W. Europe, N. Africa, |Himalayas, Formosa | | to Japan | 58. Perisoreus | 1 |N. Europe and Siberia |N. America (Urocissa | 2 |Cashmere, Japan) |Oriental genus 59. _Nucifraga_ | 3 |W. Europe to Japan, |Himalayan pine forests | | and Himalayas | 60. _Pica_ | 5 |W. Europe to China and |S. China and Formosa | | Japan | migrants[?] 61. _Cyanopica_ | 2 |Spain, N. E. Asia and | | | Japan | 62. Corvus | 12 |The whole region |Cosmopolite (excl. | | | S. Am.) 63. _Fregilus_ | 3 |W. Europe to N. China, |Abyssinian mountains | | Himalayas | | | | NECTARINIIDÆ. | | | | | | (Arachnecthra | 1 |Palestine) |Oriental genus | | | DICÆIDÆ. | | | | | | (Zosterops | 1 |Amoor and Japan) |Ethiop., Orien., | | | Austral. | | | AMPELIDÆ. | | | | | | 64. Ampelis | 2 |Northern half of region|North America | | | HIRUNDINIDÆ. | | | | | | 65. Hirundo | 2 |The whole region |Cosmopolite 66. Cotyle | 2 |The whole region (excl.|Nearctic, Ethiop., | | Atlan. Is.) | Orien. 67. Chelidon | 3 |The whole region |Oriental | | | FRINGILLIDÆ. | | | | | | 68. Fringilla | 6 |The whole region |Africa 69. _Acanthis_ | 3 |Europe and N. Africa to| | | Central Asia | 70. _Procarduelis_ | 1 |High Himalayas and | | | E. Thibet | 71. Chrysomitris | 2 |W. Europe to Japan |N. and S. America 72. _Dryospiza_ | 4 |Atlantic Islands to | | | Palestine, N. Africa | 73. _Metoponia_ | 1 |N. E. Europe to | | | W. Himalayas | 74. Chlorospiza | 5 |W. Europe, N. Africa |China, E. Africa | | to Japan | 75. Passer | 8 |The whole region |Ethiopian, Oriental 76. Montifringilla | 4 |Europe to Cashmere and | | | Siberia | 77. _Fringillauda_ | 1 |N. W. Himalayas to | | | E. Thibet, high | 78. Coccothraustes | 3 |W. Europe, High |N. America | | Himalayas to Japan | 79. _Mycerobas_ | 2 |Central Asia & High | | | Himalayas | 80. Eophona | 2 |E. Thibet, China, and |China | | Japan | 81. _Pyrrhula_ | 9 |Azores to Japan, High |Alaska | | Himalayas | (Crithagra | 1 |Palestine) |Ethiopian genus 82. Carpodacus | 12 |Cent. Eu. to Japan, |India & China, | | High Himalayas | N. Amer. 83. _Erythrospiza_ | 4 |N. Africa to | | | Afghanistan and | | | Turkestan | 84. _Uragus_ | 2 |Turkestan & E. Thibet | | | to Japan | 85. Loxia | 3 |Europe, High Himalayas |N. America | | to Japan | 86. Pinicola | 1 |N. Europe, Siberia |N. America 87. _Propyrrhula_ | 1 |High Himalayas |Darjeeling in winter 88. _Pyrrhospiza_ | 1 |Snowy Himalayas | 89. Linota | 6 |The whole region |N. America 90. Leucosticte | 4 |Turkestan to Kamschatka|N. W. America | | | Emberizinæ | | | | | | 91. {Euspiza | 4 |E. Europe to Japan |N. America 92. {_Emberiza_ | 25 |Europe to Japan |N. India, China 93. {Fringillaria | 2 |S. Europe, N. Africa |African genus 94. {Plectrophanes | 2 |Northern half of region|N. America | | | STURNIDÆ. | | | | | | 95. Pastor | 1 |East Europe, Central |India | | Asia | 96. Sturnia | 2 |Amoor, Japan, N. China |Oriental 97. Sturnus | 3 |The whole region (excl.|India, China | | Atlantic Islands) | (Amydrus | 1 |Palestine) |N. E. African genus 98. _Podoces_ | 3 |Cen. Asia, Turkestan, | | | Yarkand | | | | ALAUDIDÆ. | | | | | | 99. Otocorys | 6 |N. Europe to Japan, |India, N. America, | | N. Africa, Arabia | Andes 100. Alauda | 7 |The whole region (excl.|India, Africa | | Iceland) | 101. Galerita | 2 |Central Europe to |India, Central Africa | | N. China, N. Africa | 102. Calandrella | 4 |Central Europe to |India | | N. China, N. Africa | 103. _Melanocorypha_| 5 |S. Eu., N. Africa, |N. W. India | | N. & Cen. Asia | 104. _Pallasia_ | 1 |Mongolia | (Certhilauda | 1 |N. Africa) |S. African genus (Alaemon | 1 |N. Africa, Arabia) |Ethiopian genus 105. Ammomanes | 3 |S. Europe, N. Africa, |Africa, India | | to Cashmere | | | | MOTACILLIDÆ. | | | | | | 106. Motacilla | 6 |The whole region |Oriental, Ethiopian 107. Budytes | 4 |Europe to China |Oriental, Moluccas 108. Calobates | 2 |Atlantic Is., W. |Malaisia, Madagascar | | Europe, to China | | | | PITTIDÆ. | | | | | | (Pitta | 1 |Japan) |Oriental & Austral. | | | genus | | | PICARIÆ. | | | PICIDÆ. | | | | | | 109. Picoides | 3 |N. and Cen. Europe to |North America | | Thibet & E. Asia | 110. Picus | 16 |The whole region (excl.|India, China, N. and | | Atlantic Islands) | S. America 111. Hypopicus | 1 |N. China |Himalayas (Yungipicus | 1 |N. China) |Oriental genus 112. Dryocopus | 1 |N. & Cen. Europe to |Neotropical | | N. China | 113. Gecinus | 6 |W. Europe to Thibet, |Oriental | | Amoor & Japan | | | | YUNGIDÆ. | | | | | | 114. Yunx | 2 |W. Europe to N. W. |N. E. Africa, | | India, Thibet and | S. Africa | | Japan | | | | CUCULIDÆ. | | | | | | 115. Cuculus | 2 |The whole region (excl.|Ethiop., Oriental, | | Atlantic Islands) | Austral. 116. Coccystes | 1 |S. Europe and N. Africa|Ethiopian and Oriental | | | CORACIIDÆ. | | | | | | 117. Coracias | 1 |Cent. Europe to Cent. |Ethiopian, Oriental | | Asia | (Eurystomus | 1 |Amoor in summer) |Oriental & Austral. | | | genus | | | MEROPIDÆ. | | | | | | 118. Merops | 2 |S. Europe to Cashmere, |Ethiopian and Oriental | | N. Africa | | | | ALCEDINIDÆ. | | | | | | (Halcyon | 3 |W. Asia, N. China, |Ethiop., Orien., | | Japan) | Austral. 119. Alcedo | 2 |Europe, N. China | 120. Ceryle | 2 |S. E. Europe, Japan |Africa, India, America | | | UPUPIDÆ. | | | | | | 121. Upupa | 1 |S. Europe, N. China |Ethiop. & Oriental | | | genus | | | CAPRIMULGIDÆ. | | | | | | 122. Caprimulgus | 5 |Europe to Japan |Ethiopian and Oriental | | | CYPSELIDÆ. | | | | | | 123. Cypselus | 4 |The whole region (excl.|Ethiopian, America | | Iceland) | 124. Chætura | 2 |N. China, Dauria |Africa, India | | | COLUMBÆ. | | | COLUMBIDÆ. | | | | | | 125. Columba | 6 |The whole region |Africa, Asia, America 126. Turtur | 4 |W. Europe to Japan |Ethiopian and Oriental (Alsæcomus | 1 |E. Thibet) |Oriental genus | | | GALLINÆ. | | | PTEROCLIDÆ. | | | | | | 127. Pterocles | 2 |S. Europe, N. Africa, |Ethiopian genus | | to W. India | 128. _Syrrhaptes_ | 2 |Central Asia, N. China | | | | TETRAONIDÆ. | | | | | | 129. Francolinus | 1 |Borders of |Ethiopian, Oriental | | Mediterranean | 130. _Perdix_ | 2 |Europe to Mongolia | 131. Coturnix | 1 |Central and S. Europe |Ethiop., Orien., | | to Japan | Austral. 132. _Lerwa_ | 1 |Snowy Himalayas to | | | E. Thibet | 133. _Caccabis_ | 5 |Cen. Europe and N. |Abyssinia, Arabia | | Africa to N. W. | | | Himalayas | 134. _Tetraogallus_ | 4 |Caucasus to E. Thibet | | | and Altai Mountains | 135. Tetrao | 4 |Europe and N. Asia |N. America 136. Bonasa | 1 |Europe and N. Asia |N. America 137. Lagopus | 4 |Iceland, W. Europe to |N. America, Greenland | | Japan | | | | PHASIANIDÆ. | | | | | | 138. _Crossoptilon_ | 4 |Thibet, Mongolia, | | | N. China | 139. _Lophophorus_ | 3 |Cashmere to E. Thibet | | | (highest woods) | 140. Tetraophasis | 1 |E. Thibet |E. Thibet(?) 141. Ceriornis | 1 |N. W. Himalayas (high) |Himalayas to W. China 142. Pucrasia-- | 3 |N. W. Himalayas to |Himalayas | | N. W. China | 143. _Phasianus_ | 10 |Western Asia to Japan |W. Himalayas, Formosa 144. _Thaumalea_ | 3 |E. Thibet to Amoor, |West China | | N. China | 145. _Ithaginis_ | 2 |Nepaul to E. Thibet | | | (high) | | | | TURNICIDÆ. | | | | | | 146. Turnix | 2 |Spain and N. Africa, |Ethiop., Orien., | | N. China | Austral. | | | ACCIPITRES. | | | VULTURIDÆ. | | | | | | 147. _Vultur_ | 1 |Spain and N. Africa to | | | N. China | 148. Gyps | 1 |S. Europe, Palestine, |E. Africa, India | | Cen. Asia | 149. Otogyps | 1 |S. Europe, N. Africa |S. Africa, India 150. Neophron | 1 |Atlantic Isds. to |Africa, India | | Palestine | | | | FALCONIDÆ. | | | | | | 151. Circus | 5 |Europe to Japan |Almost Cosmopolite 152. Astur | 1 |Europe to N. China |Almost Cosmopolite 153. Accipiter | 2 |Europe to Japan |Almost Cosmopolite 154. Buteo | 4 |Europe to Japan |Cosmopolite (excl. | | | Australia) 155. Archibuteo | 1 |N. Europe to Japan |N. America 156. Gypaetus | 1 |S. Europe, N. Africa |Abyssinia, Himalayas 157. Aquila | 5 |Europe to Japan |Nearctic, Ethiop., | | | Orien. 158. Nisaetus | 2 |E. Europe, N. Africa, |India, Australia | | W. Asia | 159. Circaetus | 1 |E. and S. Europe, N. |Africa, India | | Africa, W. Asia | 160. Haliæetus | 3 |Iceland and S. Europe |Cosmopolite (excl. | | to Japan | Neotropical region) 161. Milvus | 4 |Europe to Japan, |The Old World & | | N. Africa | Austral. 162. Elanus | 2 |N. Africa, N. China to |Cosmopolite (excl. | | Amoor | East U. S.) 163. Pernis | 1 |Europe to Japan |Ethiopian and Oriental 164. Falco | 5 |The whole region |Cosmopolite (excl. | | | Pacific Islands) 165. Hierofalco | 5 |The whole region |N. America 166. Cerchneis | 4 |Atlantic Islands to |Cosmop. (excl. | | Japan | Oceania) | | | PANDIONIDÆ. | | | | | | 167. Pandion | 1 |Europe to Japan |Cosmopolite | | | STRIGIDÆ. | | | | | | 168. Surnia | 1 |N. Europe and Siberia |North America 169. Nyctea | 1 |Arctic regions |Arctic America 170. Athene | 4 |Central and S. Europe |Ethiop., Orien., | | to Japan | Austral. (Ninox | 1 |N. China and Japan) |Oriental genus 171. Glaucidium | 1 |Europe to N. China |America 172. Bubo | 2 |Europe to N. China |Africa, India, | | | America 173. Scops | 3 |S. Europe to Japan |African, Orien., | | | Austral. 174. Syrnium | 5 |Europe to Japan |African, Oriental, | | | Amer. 175. Otus | 2 |Europe to Japan |Almost Cosmopolite 176. Nyctala | 1 |N. Europe to E. Siberia|N. America 177. Strix | 1 |Europe and N. Africa |All warm & temp. | | | regions _Peculiar or very characteristic Genera of Wading and Swimming Birds._ GRALLÆ. | | | RALLIDÆ. | | | | | | _Ortygometra_ | 8 |Europe, N. E. Africa | | | | SCOLOPACIDÆ. | | | | | | _Ibidorhyncha_ | 1 |Cashmere & Cen. Asia, |Himalayan Valleys | | N. China | Terekia | 1 |N. E. Europe and |India, Australia | | Siberia | (migrant) _Helodromas_ | 1 |E. and N. Europe, | | | N. India | _Machetes_ | 1 |N. and Cen. Europe, |India in winter | | Cen. Asia | _Eurinorhynchus_ | 1 |N. E. Asia |Bengal | | | GLAREOLIDÆ. | | | | | | _Pluvianus_ | 1 |N. Africa, Spain | | | | CHARADRIIDÆ. | | | | | | Vanellus | 8 |Europe to the Punjaub |S. America | | | OTIDIDÆ. | | | | | | _Otis_ | 2 |W. Europe to Mongolia, | | | N. Africa | ANSERES. | | | ANATIDÆ. | | | | | | Aix | 1 |N. China to Amoor |N. America Bucephala | 3 |Iceland, N. Europe, and|N. America | | Asia | Histrionicus | 1 |Iceland, N. Siberia |N. America Harelda | 1 |North of whole region |Arctic America Somateria | 3 |North of whole region |N. America Oedemia | 3 |North of whole region |N. America | | | LARIDÆ. | | | | | | Rissa | 1 |North coasts of whole |N. America | | region | | | | COLYMBIDÆ. | | | | | | Colymbus | 3 |North of whole region |N. America | | | ALCIDÆ. | | | | | | Alca | 2 |North coasts of whole |N. America | | region | Fratercula | 3 |North coasts of whole |N. America | | region | Uria | 3 |North coasts of whole |N. America | | region | Mergulus | 1 |Iceland and Arctic |Arctic America | | coasts | --------------------+-----+-----------------------+---------------------- [Illustration: ETHIOPIAN REGION] {251}CHAPTER XI. THE ETHIOPIAN REGION. This is one of the best defined of the great zoological regions, consisting of tropical and South Africa, to which must be added tropical Arabia, Madagascar, and a few other islands, all popularly known as African. Some naturalists would extend the region northwards to the Atlas Mountains and include the whole of the Sahara; but the animal life of the northern part of that great desert seems more akin to the Palæarctic fauna of North Africa. The Sahara is really a debatable land which has been peopled from both regions; and until we know more of the natural history of the great plateaus which rise like islands in the waste of sand, it will be safer to make the provisional boundary line at or near the tropic, thus giving the northern half to the Palæarctic, the southern to the Ethiopian region. The same line may be continued across Arabia. With our present imperfect knowledge of the interior of Africa, only three great continental sub-regions can be well defined. The open pasture lands of interior tropical Africa are wonderfully uniform in their productions; a great number of species ranging from Senegal to Abyssinia and thence to the Zambesi, while almost all the commoner African genera extend over the whole of this area. Almost all this extensive tract of country is a moderately elevated plateau, with a hot and dry climate, and characterised by a grassy vegetation interspersed with patches of forest. This forms our first or East African sub-region. The whole of the west coast from the south side of the Gambia River to about 10° or 12° south latitude, is a very {252}different kind of country; being almost wholly dense forests where not cleared by man, and having the hot moist uniform climate, and perennial luxuriance of vegetation, which characterise the great equatorial belt of forest all round the globe. This forest country extends to an unknown distance inland, but it was found, with its features well marked, by Dr. Schweinfurth directly he crossed the south-western watershed of the Nile; and far to the south we find it again unmistakably indicated, in the excessively moist forest country about the head waters of the Congo, where the heroic Livingstone met his death. In this forest district many of the more remarkable African types are alone found, and its productions occasionally present us with curious similarities to those of the far removed South American or Malayan forests. This is our second or West African sub-region. Extra-tropical South Africa possesses features of its own, quite distinct from those of both the preceding regions (although it has also much in common with the first). Its vegetation is known to be one of the richest, most peculiar, and most remarkable on the globe; and in its zoology it has a speciality, similar in kind but less in degree, which renders it both natural and convenient to separate it as our third, or South African sub-region. Its limits are not very clearly ascertained, but it is probably bounded by the Kalahari desert on the north-west, and by the Limpopo Valley, or the mountain range beyond, on the north-east, although some of its peculiar forms extend to Mozambique. There remains the great Island of Madagascar, one of the most isolated and most interesting on the globe, as regards its animal productions; and to this must be added, the smaller islands of Bourbon, Mauritius and Rodriguez, the Seychelles and the Comoro Islands, forming together the Mascarene Islands,--the whole constituting our fourth sub-region. _Zoological Characteristics of the Ethiopian Region._--We have now to consider briefly, what are the peculiarities and characteristics of the Ethiopian Region as a whole,--those which give it its distinctive features and broadly separate it from the other primary zoological regions. {253}_Mammalia._--This region has 9 peculiar families of mammalia. Chiromyidæ (containing the aye-aye); Potamogalidæ and Chrysochloridæ (Insectivora); Cryptoproctidæ and Protelidae (Carnivora); Hippopotamidæ and Camelopardalidæ (Ungulata); and Orycteropodidæ (Edentata). Besides these it possesses 7 peculiar genera of apes, _Troglodytes_, _Colobus_, _Myiopithecus_, _Cercopithecus_, _Cercocebus_, _Theropithecus_, and _Cynocephalus_; 2 sub-families of lemurs containing 6 genera, confined to Madagascar, with 3 genera of two other sub-families confined to the continent; of Insectivora a family, Centetidæ, with 5 genera, peculiar to Madagascar, and the genera _Petrodromus_ and _Rhynchocyon_ belonging to the Macroscelididæ, or elephant-shrews, restricted to the continent; numerous peculiar genera or sub-genera of civets; _Lycaon_ and _Megalotis_, remarkable genera of Canidæ; _Ictonyx_, the zorilla, a genus allied to the weasels; 13 peculiar genera of Muridæ; _Pectinator_, a genus of the South American family Octodontidæ; and 2 genera of the South American Echimyidæ or spiny rats. Of abundant and characteristic groups it possesses _Macroscelides_, _Felis_, _Hyæna_, _Hyrax_, _Rhinoceros_, and _Elephas_, as well as several species of zebra and a great variety of antelopes. The great speciality indicated by these numerous peculiar families and genera, is still farther increased by the absence of certain groups dominant in the Old-World continent, an absence which we can only account for by the persistence, through long epochs, of barriers isolating the greater part of Africa from the rest of the world. These groups are, Ursidæ, the bears; Talpidæ the moles; Camelidæ, the camels; Cervidæ, the deer; Caprinæ, the goats and sheep; and the genera _Bos_ (wild ox); and _Sus_ (wild boar). Combining these striking deficiencies, with the no less striking peculiarities above enumerated, it seems hardly possible to have a region more sharply divided from the rest of the globe than this is, by its whole assemblage of mammalia. _Birds._--In birds the Ethiopian region is by no means so strikingly peculiar, many of these having been able to pass the ancient barriers which so long limited the range of mammalia. {254}It is, however, sufficiently rich, possessing 54 families of land birds, besides a few genera whose position is not well ascertained, and which may constitute distinct families. Of these 6 are peculiar, Musophagidæ (the plantain eaters); Coliidæ (the colies); Leptosomidæ, allied to the cuckoos; Irrisoridæ, allied to the hoopoes; and Serpentaridæ, allied to the hawks. Only one Passerine family is peculiar--Paictidæ, while most of the other tropical regions possess several; but _Euryceros_ and _Buphaga_, here classed with the Sturnidæ, ought, perhaps, to form two more. It has, however, many peculiar genera, especially among the fruit-thrushes, Pycnonotidæ; flycatchers, Muscicapidæ; shrikes, Lanidæ; crows, Corvidæ; starlings, Sturnidæ; and weaver-birds, Ploceidæ; the latter family being very characteristic of the region. It is also rich in barbets, Megalæmidæ (7 peculiar genera); cuckoos, Cuculidæ; rollers, Coraciidæ; bee-eaters, Meropidæ; hornbills, Bucerotidæ; and goat-suckers, Caprimulgidæ. It is poor in parrots and rather so in pigeons; but it abounds in _Pterocles_ and _Francolinus_, genera of Gallinæ, and possesses 4 genera of the peculiar group of the guinea-fowls, forming part of the pheasant family. It abounds in vultures, eagles, and other birds of prey, among which is the anomalous genus _Serpentarius_, the secretary-bird, constituting a distinct family. Many of the most remarkable forms are confined to Madagascar and the adjacent islands, and will be noticed in our account of that sub-region. _Reptiles._--Of the reptiles there are 4 peculiar Ethiopian families;--3 of snakes, Rachiodontidæ, Dendraspidæ, and Atractaspidæ and 1 of lizards, Chamæsauridæ. Psammophidæ (desert snakes) are abundant, as are Lycodontidæ (fanged ground-snakes), and Viperidæ (vipers). The following genera of snakes are peculiar or highly characteristic:--_Leptorhynchus_, _Rhamnophis_, _Herpetethiops_ and _Grayia_ (Colubridæ); _Hopsidrophis_ and _Bucephalus_ (Dendrophidæ); _Langalia_ (Dryophidæ); _Pythonodipsas_ (Dipsadidæ); _Boedon_, _Lycophidion_, _Holuropholis_, _Simocephalus_ and _Lamprophis_ (Lycodontidæ); _Hortulia_ and _Sanzinia_ (Pythonidæ); _Cyrptophis_, _Elapsoidea_ and _Poecilophis_ (Elapidæ); and _Atheris_ (Viperidæ). The following genera {255}of lizards are the most characteristic:--_Monotrophis_ (Lepidosternidæ); _Cordylus_, _Pseudocordylus_, _Platysaurus_, _Cordylosaurus_, _Pleurostichus_, _Saurophis_ and _Zonurus_ (Zonuridæ); _Sphænops_, _Scelotes_, _Sphænocephalus_ and _Sepsina_ (Sepidæ); _Pachydactylus_ (Geckotidæ); _Agama_ (Agamidæ); and _Chameleon_ (Chameleonidæ). Of tortoises, _Cynyxis_, _Pyxis_ and _Chersina_ (Testudinidæ), and _Cycloderma_ (Trionychidæ) are the most characteristic. _Amphibia._--Of the 9 families of amphibia there is only 1 peculiar, the Dactylethridæ, a group of toads; but the Alytidæ, a family of frogs, are abundant. _Fresh-water Fish._--Of the 14 families of fresh-water fishes 3 are peculiar: Mormyridæ and Gymnarchidæ, small groups not far removed from the pikes; and Polypteridæ, a small group of ganoid fishes allied to the gar-pikes (Lepidosteidæ) of North America. _Summary of Ethiopian Vertebrates._--Combining the results here indicated and set forth in greater detail in the tables of distribution, we find that the Ethiopian region possesses examples of 44 families of mammalia, 72 of birds, 35 of reptiles, 9 of amphibia, and 15 of fresh-water fishes. It has 23 (or perhaps 25) families of Vertebrata altogether peculiar to it out of a total of 175 families, or almost exactly one-eighth of the whole. Out of 142 genera of mammalia found within the region, 90 are peculiar to it; a proportion not much short of two-thirds. Of land birds there are 294 genera, of which 179 are peculiar; giving a proportion of a little less than three-fifths. Compared with the Oriental region this shows a considerably larger amount of speciality under all the heads; but the superiority is mainly due to the wonderful and isolated fauna of Madagascar, to which the Oriental region has nothing comparable. Without this the regions would be nearly equal. _Insects: Lepidoptera._--11 out of the 16 families of butterflies have representatives in Africa, but none are peculiar. Acræidæ is one of the most characteristic families, and there {256}are many interesting forms of Nymphalidæ, Lycænidæ, and Papilionidæ. The peculiar or characteristic forms are _Amauris_ (Danaidæ); _Gnophodes_, _Leptoneura_, _Bicyclus_, _Heteropsis_ and _Coenyra_ (Satyridæ); _Acræa_ (Acræidæ); _Lachnoptera_, _Precis_, _Salamis_, _Crenis_, _Godartia_, _Amphidema_, _Pseudacræa_, _Catuna_, _Euryphene_, _Romalæosoma_, _Hamanumida_, _Aterica_, _Harma_, _Meneris_, _Charaxes_, and _Philognoma_ (Nymphalidæ); _Pentila_, _Liptena_, _Durbania_, _Zeritis_, _Capys_, _Phytala_, _Epitola_, _Hewitsonia_ and _Deloneura_ (Lycænidæ); _Pseudopontia_, _Idmais_, _Teracolus_, _Callosune_ (Pieridæ); _Abantis_, _Ceratrichia_ and _Caprona_ (Hesperidæ). The total number of species known is about 750; which is very poor for an extensive tropical region, but this is not to be wondered at when the nature of much of the country is considered. It is also, no doubt, partly due to our comparative ignorance of the great equatorial forest district, which is the only part likely to be very productive in this order of insects. _Coleoptera._--In our first representative family, Cicindelidæ or tiger-beetles, the Ethiopian region is rather rich, having 13 genera, 11 of which are peculiar to it; and among these are such remarkable forms as _Manticora_, _Myrmecoptera_ and _Dromica_; with _Megacephala_, a genus only found elsewhere in Australia and South America. In Carabidæ or carnivorous ground beetles, there are about 75 peculiar genera. Among the most characteristic are _Anthia_, _Polyrhina_, _Graphipterus_ and _Piezia_, which are almost all peculiar; while _Orthogonius_, _Hexagonia_, _Macrochilus_, _Thyreopterus_, _Eudema_, and _Abacetus_ are common to this and the Oriental region; and _Hypolithus_ to the Neotropical. Out of 27 genera of Buprestidæ, or metallic beetles, only 6 are peculiar to the region, one of the most remarkable being _Polybothrus_, confined to Madagascar. _Sternocera_ and _Chrysochroa_ are characteristic of this region and the Oriental; it has _Julodis_ in common with the Mediterranean sub-region, and _Belionota_ with the Malayan. The region is not rich in Lucanidæ, or stag-beetles, possessing only 10 genera, 7 of which are peculiar, but most of them {257}consist of single species. The other three genera, _Cladognathus_, _Nigidius_, and _Figulus_, are the most characteristic, though all have a tolerably wide range in the Old World. In the elegant Cetoniidæ, or rose-chafers, this region stands preeminent, possessing 76 genera, 64 of which are peculiar to it. The others are chiefly Oriental, except _Oxythræa_ which is European, and _Stethodesma_ which is Neotropical. Preeminent in size and beauty is _Goliathus_, comprising perhaps the most bulky of all highly-coloured beetles. Other large and characteristic genera are _Ceratorhina_, _Ischnostoma_, _Anochilia_, _Diplognatha_, _Agenius_, and many others of less extent. In the enormous tribe of Longicorns, or long-horned beetles, the Ethiopian is not so rich as the other three tropical regions; but this may be, in great part, owing to its more productive districts having never been explored by any competent entomologists. It nevertheless possesses 262 genera, 216 of which are peculiar, the others being mostly groups of very wide range. Out of such a large number it is difficult to select a few as most characteristic, but some of the peculiarities of distribution as regards other regions may be named. Among Prionidæ, _Tithoes_ is a characteristic Ethiopian genus. A few species of the American genera _Parandra_ and _Mallodon_ occur here, while the North Temperate genus _Prionus_ is only found in Madagascar. Among Cerambycidæ, _Promeces_ is the most characteristic. The American genera _Oeme_ and _Cyrtomerus_ occur; while _Homalachnus_ and _Philagathes_ are Malayan, and _Leptocera_ occurs only in Madagascar, Ceylon, Austro-Malaya, and Australia. The Lamiidæ are very fine; _Sternotomis_, _Tragocephala_, _Ceroplesis_, _Phryncta_, _Volumnia_, and _Nitocris_, being very abundant and characteristic. Most of the non-peculiar genera of this family are Oriental, but _Spalacopsis_ and _Acanthoderes_ are American, while _Tetraglenes_ and _Schoenionta_ have been found only in East and South Africa and in Malaya. _Terrestrial Mollusca_.--In the extensive family of the Helicidæ or snails, 13 genera are represented, only one of which, _Columna_, is peculiar. This region is however the metropolis of _Achatina_, some of the species being the largest land-shells {258}known. _Buliminus_, _Stenogyra_, and _Pupa_ are characteristic genera. _Bulimus_ is absent, though one species inhabits St. Helena. The operculated shells are not very well represented, the great family of Cyclostomidæ having here only nine genera, with but one peculiar, _Lithidion_, found in Madagascar, Socotra, and Arabia. None of the genera appear to be well represented throughout the region, and they are almost or quite absent from West Africa. According to Woodward's _Manual_ (1868) West Africa has about 200 species of land-shells, South Africa about 100, Madagascar nearly 100, Mauritius about 50. All the islands have their peculiar species; and are, in proportion to their extent, much richer than the continent; as is usually the case. THE ETHIOPIAN SUB-REGIONS. It has been already explained that these are to some extent provisional; yet it is believed that they represent generally the primary natural divisions of the region, however they may be subdivided when our knowledge of their productions becomes more accurate. _I. The East African Sub-region, or Central and East Africa._ This division includes all the open country of tropical Africa south of the Sahara, as well as an undefined southern margin of that great desert. With the exception of a narrow strip along the east coast and the valleys of the Niger and Nile, it is a vast elevated plateau from 1,000 to 4,000 feet high, hilly rather than mountainous, except the lofty table land of Abyssinia, with mountains rising to 16,000 feet and extending south to the equator, where it terminates in the peaks of Kenia and Kilimandjaro, 18,000 and 20,000 feet high. The northern portion of this sub-region is a belt about 300 miles wide between the Sahara on the north and the great equatorial forest on the south, extending from Cape Verd, the extreme western point of Africa, across the northern bend of the Niger and Lake Tchad to the mountains of Abyssinia. The greater part of this tract has a {259}moderate elevation. The eastern portion reaches from about the second cataract of the Nile, or perhaps from about the parallel of 20° N. Latitude, down to about 20° S. Latitude, and from the east coast to where the great forest region commences, or to Lake Tanganyika and about the meridian of 28° to 30° E. Longitude. The greater part of this tract is a lofty plateau. The surface of all this sub-region is generally open, covered with a vegetation of high grasses or thorny shrubs, with scattered trees and isolated patches of forest in favourable situations. The only parts where extensive continuous forests occur, are on the eastern and western slopes of the great Abyssinian plateau, and on the Mozambique coast from Zanzibar to Sofala. The whole of this great district has one general zoological character. Many species range from Senegal to Abyssinia, others from Abyssinia to the Zambesi, and a few, as _Mungos fasciatus_ and _Phacochoerus æthiopicus_, range over the entire sub-region. _Fennecus_, _Ictonyx_, and several genera of antelopes, characterise every part of it, as do many genera of birds. _Coracias nævia_, _Corythornis cyanostigma_, _Tockus nasutus_, _T. erythrorhynchus_, _Parus leucopterus_, _Buphaga africana_, _Vidua paradisea_, are examples of _species_, which are found in the Gambia, Abyssinia and South East Africa, but not in the West African sub-region; and considering how very little is known of the natural history of the country immediately south of the Sahara, it may well be supposed that these are only a small portion of the species really common to the whole area in question, and which prove its fundamental unity. Although this sub-region is so extensive and so generally uniform in physical features, it is by far the least peculiar part of Africa. It possesses, of course, all those wide-spread Ethiopian types which inhabit every part of the region, but it has hardly any special features of its own. The few genera which are peculiar to it have generally a limited range, and for the most part belong, either to the isolated mountain-plateau of Abyssinia which is almost as much Palæarctic as Ethiopian, or to the woody districts of Mozambique where the fauna has more of a West or South African character. {260}_Mammalia._--The only forms of Mammalia peculiar to this sub-region are _Theropithecus_, one of the Cynopithecidæ confined to Abyssinia; _Petrodromus_ and _Rhynchocyon_, belonging to the insectivorous Macroscelididæ, have only been found in Mozambique; the Antelopine genus _Neotragus_, from Abyssinia southward; _Saccostomus_ and _Pelomys_ genera of Muridæ inhabiting Mozambique; _Heterocephalus_ from Abyssinia, and _Heliophobius_ from Mozambique, belonging to the Spalacidæ; and _Pectinator_ from Abyssinia, belonging to the Octodontidæ. _Cynocephalus_, _Rhinoceros_, _Camelopardalis_, and antelopes of the genera _Oryx_, _Cervicapra_, _Kobus_, _Nanotragus_, _Cephalophus_, _Hippotragus_, _Alcephalus_, and _Catoblepas_, are characteristic; as well as _Felis_, _Hyæna_, and numerous civets and ichneumons. _Birds._--Peculiar forms of birds are hardly to be found here; we only meet with two--_Hypocolius_, a genus of shrikes in Abyssinia; and _Balæniceps_, the great boat-billed heron of the Upper Nile. Yet throughout the country birds are abundant, and most of the typical Ethiopian forms are well represented. _Reptiles._--Of reptiles, the only peculiar forms recorded are _Xenocalamus_, a genus of snakes, belonging to the Calamariidæ; and _Pythonodipsas_, one of the Dipsadidæ, both from the Zambesi; and among lizards, _Pisturus_, one of the Geckotidæ, from Abyssinia. _Amphibia and Fishes._--There are no peculiar forms of amphibia or of fresh-water fishes. _Insects._--Insects are almost equally unproductive of peculiar forms. Among butterflies we have _Abantis_, one of the Hesperidæ, from Mozambique; and in Coleoptera, 2 genera of Cicindelidæ, 8 of Carabidæ, 1 or 2 of Cetoniidæ, and about half-a-dozen of Longicorns: a mere nothing, as we shall see, compared with the hosts of peculiar genera that characterise each of the other sub-regions. Neither do land-shells appear to present any peculiar forms. The fact that so very few special types characterise the extensive area now under consideration is very noteworthy. It justifies us in uniting this large and widespread tract of country as forming essentially but one sub-division of the great Ethiopian region, and it suggests some curious speculations as to the former history of that region, a subject which must be deferred to the latter part of this chapter. In none of the other great tropical regions does it occur, that the largest portion of their area, although swarming with life, yet possesses hardly any distinctive features except the absence of numerous types characteristic of the other sub-regions. Plate IV. [Illustration] CHARACTERISTIC ANIMALS OF EAST AFRICA. {261}_Plate IV._--_Illustrating the Zoology of East Africa._--Although this sub-region has so little speciality, it is that which abounds most in large animals, and is, perhaps, the best representative of Africa as regards zoology. Some of the most distinctive of African animals range over the whole of it, and as, from recent explorations, many parts of this wide area have been made known to the reading public, we devote one of our plates to illustrate the especially African forms of life that here abound. The antelopes represented are the koodoo (_Tragelaphus strepsiceros_) one of the handsomest of the family, which ranges over all the highlands of Africa from Abyssinia to the southern districts. To the left is the aardvark, or earth pig, of North Eastern Africa (_Orycteropus æthiopicus_) which, to the north of the equator in East Africa, represents the allied species of the Cape of Good Hope. These Edentata are probably remnants of the ancient fauna of Africa, when it was completely isolated from the northern continents and few of the higher types had been introduced. The large bird in the foreground is the secretary-bird, or serpent-killer (_Serpentarius reptilivorus_), which has affinities both for the birds-of-prey and the waders. It is common over almost all the open country of Africa, destroying and feeding on the most venomous serpents. The bird on the wing is the red-billed promerops (_Irrisor erythrorhynchus_), a handsome bird with glossy plumage and coral-red bill. It is allied to the hoopoes, and feeds on insects which it hunts for among the branches of trees. This species also ranges over a large part of east and central Africa to near the Cape of Good Hope. Other species are found in the west; and the genus, which forms a distinct family, _Irrisoridæ_, is one of the best marked Ethiopian types of birds. In the distance is a rhinoceros, now one of the characteristic features of African {262}zoology, though there is reason to believe that it is a comparatively recent intruder into the country. _II. The West-African Sub-region._ This may be defined as the equatorial-forest sub-region, since it comprises all that portion of Africa, from the west coast inland, over which the great equatorial forests prevail more or less uninterruptedly. These commence to the south of the Gambia River, and extend eastwards in a line roughly parallel to the southern margin of the great desert, as far as the sources of the upper Nile and the mountains forming the western boundary of the basin of the great lakes; and southward to that high but marshy forest-country in which Livingstone was travelling at the time of his death. Its southern limits are undetermined, but are probably somewhere about the parallel of 11° S. Latitude.[10] This extensive and luxuriant district has only been explored zoologically in the neighbourhood of the West coast. Much, no doubt, remains to be done in the interior, yet its main features are sufficiently well known, and most of its characteristic types of animal life have, no doubt, been discovered. _Mammalia._--Several very important groups of mammals are peculiar to this sub-region. Most prominent are the great anthropoid apes--the gorilla and the chimpanzee--forming the genus _Troglodytes_; and monkeys of the genera _Myiopithecus_ and _Cercocebus_. Two remarkable forms of lemurs, _Perodicticus_ and _Arctocebus_, are also peculiar to West Africa. Among the Insectivora is _Potamogale_, a semi-aquatic animal, forming a distinct family; and three peculiar genera of civets (Viverridæ) have been described. _Hyomoschus_, a small, deer-like animal, belongs to the Tragulidæ, or chevrotains, a family otherwise {263}confined to the Oriental region; and in the squirrel family is a curious genus, _Anomalurus_, which resembles the flying squirrels of other parts of the world, without being directly allied to them. _Birds._--In this class we find a larger proportionate number of peculiar forms. _Hypergerus_ and _Alethe_, belonging to the Timaliidæ, or babblers, are perhaps allied to Malayan groups; _Parinia_, a peculiar form of tit, is found only in Prince's Island; _Ixonotus_ is an abundant and characteristic form of Pycnonotidæ; _Fraseria_, _Hypodes_, _Cuphopterus_, and _Chaunonotus_, are peculiar genera of shrikes; _Picathartes_ is one of the many strange forms of the crow family; _Cinnyricinclus_ is a peculiar genus of sun-birds; _Pholidornis_ is supposed to belong to the Oriental Dicæidæ, or flower-peckers; _Waldenia_ is a recently-described new form of swallow; _Ligurnus_, a finch, _Spermospiga_, a weaver bird, and _Onychognathus_ a starling, are also peculiar West African genera. Coming to the Picariæ we have _Verreauxia_, a peculiar woodpecker; three peculiar genera of barbets (Megalæmidæ); the typical plantain-eaters (Musophaga); _Myioceyx_, a peculiar genus of kingfishers; while _Berenicornis_ is a genus of crested hornbills, only found elsewhere in Malaya. The grey parrots, of the genus _Psittacus_, are confined to this sub-region, as are two peculiar genera of partridges, and three of guinea-fowl. We have also here a species of _Pitta_, one of the Oriental family of ground-thrushes; and the Oriental paroquets, _Palæornis_, are found here as well as in Abyssinia and the Mascarene Islands. We thus find, both in the Mammalia and birds of West Africa, a special Oriental or even Malayan element not present in the other parts of tropical Africa, although appearing again in Madagascar. In the Mammalia it is represented by the anthropoid apes; by _Colobus_ allied to _Semnopithecus_, and by _Cercocebus_ allied to _Macacus_; and especially by a form of the Malayan family of chevrotains (Tragulidæ). The Malayan genus of otters, _Aonyx_, is also said to occur in West and South Africa. In birds we have special Oriental and Malayan affinities in _Alethe_, _Pholidornis_, _Berenicornis_, _Pitta_, and _Palæornis;_ while the Oriental genus _Treron_ has a wide range in Africa. We shall {264}endeavour to ascertain the meaning of this special relation at a subsequent stage of our inquiries. _Plate V._--_River Scene in West Africa, with Characteristic Animals._--Our artist has here well represented the luxuriance and beauty of a tropical forest; and the whole scene is such as might be witnessed on the banks of one of the rivers of equatorial West Africa. On the right we see a red river-hog (_Potamochoerus penicillatus_), one of the handsomest of the swine family, and highly characteristic of the West African sub-region. In a tree overhead is the potto (_Perodicticus potto_), one of the curious forms of lemur confined to West Africa. On the left is the remarkable _Potamogale velox_, first discovered by Du Chaillu,--an Insectivorous animal, with the form and habits of an otter. On the other side of the river are seen a pair of gorillas (_Troglodytes gorilla_), the largest of the anthropoid apes. The bird on the wing is the Whydah finch (_Vidua paradisea_), remarkable for the enormous plumes with which the tail of the male bird is decorated during the breeding season. The crested bird overhead is one of the beautiful green touracos (_Turacus macrorhynchus_), belonging to the Musophagidæ, or plantain-eaters, a family wholly African, and most abundant in the western sub-region. _Reptiles._--In this class we find a large number of peculiar forms; 13 genera of snakes, 3 of lizards, and 2 of tortoises being confined to the sub-region. The snakes are _Pariaspis_, _Elapops_, and _Prosymna_ (Calamariidæ), _Rhamnophis_, _Herpetethiops_, and _Grayia_ (Colubridæ), _Neusterophis_ and _Limnophis_ (Homalopsidæ), _Simocephalus_ and _Holurophis_ (Lycodontidæ); _Pelophilus_ (Pythonidæ); _Elapsoidea_ (Elapidæ); and _Atheris_ (Viperidæ). The lizards are _Dalophia_ (Lepidosternidæ); _Otosaurus_ (Scincidæ); _Psilodactylus_ (Geckotidæ). The tortoises, _Cinyxis_ (Testudinidæ) and _Tetrathyra_ (Trionichidæ). _Amphibia._--Of Amphibia, there are 2 peculiar genera of tree-frogs, _Hylambatis_ and _Hemimantis_, belonging to the Polypedatidæ. Plate V. [Illustration] SCENE IN WEST AFRICA, WITH CHARACTERISTIC ANIMALS. {265}Here, too, we find some interesting relations with the Oriental region on the one side, and the Neotropical on the other. The snakes of the family Homalopsidæ have a wide range, in America, Europe, and all over the Oriental region, but are confined to West Africa in the Ethiopian region. _Dryiophis_ (Dryiophidæ) and _Dipsadoboa_ (Dipsadidæ) on the other hand, are genera of tropical America which occur also in West Africa. The family of lizards, Acontiadæ, are found in West and South Africa, Ceylon, and the Moluccas. The family of toads, Engystomidæ, in West and South Africa and the whole Oriental region; while the Phryniscidæ inhabit tropical Africa and Java. _Insects._--We have here a large number of peculiar genera. There are 10 of butterflies, _Lachnoptera_, _Amphidema_, and _Catuna_ belonging to the Nymphalidæ, while four others are Lycænidæ. The genus _Euxanthe_ is common to West Africa and Madagascar. Of Coleoptera there are 53 peculiar genera; 20 are Carabidæ, 2 Lucanidæ, 12 Cetoniidæ, 3 Prionidæ, 16 Cerambycidæ, and 34 Lamiidæ. Besides these there are 4 or 5 genera confined to West Africa and Madagascar. _Land Shells._--West Africa is very rich in land shells, but it does not appear to possess any well-marked genera, although several of the smaller groups or sub-genera are confined to it. Helicidæ of the genera _Nanina_, _Buliminus_ and _Achatina_ are abundant and characteristic. _Islands of the West African Sub-region._--The islands in the Gulf of Guinea are, Fernando Po, very near the main land, with Prince's Island and St. Thomas, considerably further away to the south-west. Fernando Po was once thought to be a remarkable instance of an island possessing a very peculiar fauna, although close to the main land and not divided from it by a deep sea. This, however, was due to our having obtained considerable collections from Fernando Po, while the opposite coast was almost unknown. One after another the species supposed to be peculiar have been found on the continent, till it becomes probable, that, as in the case of other islands similarly situated, it contains no peculiar species whatever. The presence of numerous mammalia, among which are baboons, lemurs, _Hyrax_, and {266}_Anomalurus_, shows that this island has probably once been united to the continent. Prince's Island, situated about 100 miles from the coast, has no mammals, but between 30 and 40 species of birds. Of these 7 are peculiar species, viz., _Zosterops ficedulina_, _Cuphopterus dohrni_ (a peculiar genus of Sylviidæ), _Symplectes princeps_, _Crithagra rufilata_, _Columba chlorophæa_, _Peristera principalis_, and _Strix thomensis_. In the Island of St. Thomas, situated on the equator about 150 miles from the coast, there are 6 peculiar species out of 30 known birds, viz., _Scops leucopsis_, _Zosterops lugubris_, _Turdus olivaceofuscus_, _Oriolus crassirostris_, _Symplectes sancti-thomæ_ and _Aplopelia simplex_; also _Strix thomensis_ in common with Prince's Island. The remainder are all found on the adjacent coasts. It is remarkable that in Prince's Island there are no birds of prey, any that appear being driven off by the parrots (_Psittacus erithacus_) that abound there; whereas in St. Thomas and Fernando Po they are plentiful. _III. South-African Sub-region._ This is the most peculiar and interesting part of Africa, but owing to the absence of existing barriers its limits cannot be well defined. The typical portion of it hardly contains more than the narrow strip of territory limited by the mountain range which forms the boundary of the Cape Colony and Natal, while in a wider sense it may be extended to include Mozambique. It may perhaps be best characterised as bounded by the Kalahari desert and the Limpopo river. It is in the more limited district of the extreme south, that the wonderful Cape flora alone exists. Here are more genera and species, and more peculiar types of plants congregated together, than in any other part of the globe of equal extent. There are indications of a somewhat similar richness and specialization in the zoology of this country; but animals are so much less closely dependent on soil and climate, that much of the original peculiarity has been obliterated, by long continued interchange of species with so vast an area as {267}that of Africa south of the equator. The extreme peculiarity and isolation of the flora must not, however, be lost sight of, if we would correctly interpret the phenomena afforded by the distribution of animal life on the African continent. _Mammalia._--A much larger number of peculiar forms of mammals are found here than in any of the other sub-regions, although it is far less in extent than either of the three divisions of the continent. Among Insectivora we have the Chrysochloridæ, or golden moles, consisting of two genera confined to South Africa; while the Macroscelididæ, or elephant shrews, are also characteristically South African, although ranging as far as Mozambique and the Zambezi, with one outlying species in North Africa. The Viverridæ are represented by three peculiar genera, _Ariela_, _Cynictis_, and _Suricata_. The Carnivora present some remarkable forms: _Proteles_, forming a distinct family allied to the hyænas and weasels; and two curious forms of Canidæ--_Megalotis_ (the long-eared fox) and _Lycaon_ (the hyæna-dog), the latter found also in parts of East Africa. _Hydrogale_ is a peculiar form of Mustelidæ; _Pelea_ one of the antelopes; _Dendromys_, _Malacothrix_, and _Mystromys_ are peculiar genera of the mouse family (Muridæ); _Bathyerges_ one of the mole-rats (Spalacidæ); _Pedetes_, the Cape-hare, a remarkable form of jerboa; and _Petromys_, one of the spiny-rats (Echimyidæ). The remarkable _Orycteropus_, or earth-pig, has one species in South and one in North East Africa. We have thus eighteen genera of mammalia almost or quite peculiar to South Africa. _Birds._--These do not present so many peculiar forms, yet some are very remarkable. _Chætops_ is an isolated genus of thrushes (Turdidæ). _Lioptilus_, one of the fruit-thrushes (Pycnonotidæ). _Pogonocichla_, one of the fly-catchers; _Urolestes_, a shrike; _Promerops_, a sun-bird; _Philetærus_ and _Chera_, weaver-birds; and three peculiar genera of larks--_Spizocorys_, _Heterocorys_, and _Tephrocorys_, complete the list of peculiar types of Passeres. A wood-pecker, _Geocolaptes_, is nearly allied to a South American genus. The Cape-dove, _Oena_, is confined to South and East Africa and Madagascar; and _Thalassornis_ is a peculiar form of duck. Several genera are also confined to West and South {268}Africa;--as _Phyllastrephus_ (Pycnonotidæ), _Smithornis_ (Muscicapidæ), _Corvinella_ (Laniidæ); _Barbatula_ and _Xylobucco_ (Megalæmidæ); _Ceuthmochares_, also in Madagascar, (Cuculidæ); _Typanistria_ (Columbidæ). Other remarkable forms, though widely spread over Africa, appear to have their metropolis here, as _Colius_ and _Indicator_. Others seem to be confined to South Africa and Abyssinia, as the curious _Buphaga_ (Sturnidæ); and _Apaloderma_ (Trogonidæ). _Machærhamphus_ (Falconidæ) is found only in South-West Africa, Madagascar, and the Malay Peninsula. _Reptiles._--There are 4 peculiar genera of snakes,--_Typhline_, belonging to the blind burrowing snakes, Typhlopidæ; _Lamprophis_ (Lycodontidæ); _Cyrtophis_ and _Pæcilophis_ (Elapidæ), a family which is chiefly Oriental and Australian. Of Lizards there are 10 peculiar genera; _Monotrophis_ (Lepidosternidæ), but with an allied form in Angola; _Cordylus_, _Pseudocordylus_, _Platysaurus_, _Cordylosaurus_, _Pleurostichus_, and _Saurophis_, all peculiar genera of Zonuridæ; _Chamæsaura_, forming the peculiar family Chamæsauridæ; _Colopus_ and _Rhopitropus_ (Geckotidæ). _Amphibia._--Of Amphibia there are 4 peculiar genera: _Schismaderma_ (Bufonidæ); _Brachymerus_ (Engystomidæ); _Phrynobatrachus_ and _Stenorhynchus_ (Ranidæ). These last are allied to Oriental genera, and the only other Engystomidæ are Oriental and Neotropical. _Fresh-water Fish._--Of fresh-water fishes there is 1 genus--_Abrostomus_--belonging to the carp family, peculiar to South Africa. _Insects._--South Africa is excessively rich in insects, and the number of peculiar types surpasses that of any other part of the region. We can only here summarize the results. _Lepidoptera._--Of butterflies there are 7 peculiar genera; 2 belonging to the Satyridæ, 1 to Acræidæ, 3 to Lycænidæ, and 1 to Hesperidæ. _Zeritis_ (Lycænidæ) is also characteristic of this sub-region, although 1 species occurs in West Africa. _Coleoptera._--These are very remarkable. In the family of Cicindelidæ, or tiger-beetles, we have the extraordinary _Manticora_ and _Platychile_, forming a sub-family, whose nearest allies are in North America; as well as _Ophryodera_ and _Dromica_, the latter an extensive genus, which ranges as far north as Mozambique {269}and Lake Ngami. Another genus of this family, _Jansenia_, is common to South Africa and South India. In the large family of Carabidæ, or ground-beetles, there are 17 peculiar South African genera, the most important being _Crepidogaster_, _Hytrichopus_, _Arsinoë_, and _Piezia_. Three others--_Eunostus_, _Glyphodactyla_, and _Megalonychus_--are common to South Africa and Madagascar only. There is also a genus in common with Java, and one with Australia. Of Lucanidæ, or stag-beetles, there are 3 peculiar genera; of Cetoniidæ, or rose-chafers, 14; and of Buprestidæ, 2. In the great family of Longicorns there are no less than 67 peculiar genera--an immense number when we consider that the generally open character of the country, is such as is not usually well suited to this group of insects. They consist of 5 peculiar genera of Prionidæ, 25 of Cerambycidæ, and 37 of Lamiidæ. _Summary of South-African Zoology._--Summarizing these results, we find that South Africa possesses 18 peculiar genera of Mammalia, 12 of Birds, 18 of Reptiles, 1 of Fishes, 7 of Butterflies, and 107 of the six typical families of Coleoptera. Besides this large amount of speciality it contains many other groups, which extend either to West Africa, to Abyssinia, or to Madagascar only, a number of which are no doubt to be referred as originating here. We also find many cases of direct affinity with the Oriental region, and especially with the Malay districts, and others with Australia; and there are also less marked indications of a relation to America. _Atlantic Islands of the Ethiopian Region._ _St. Helena._--The position of St. Helena, about 1,000 miles west of Africa and 16° south of the equator, renders it difficult to place it in either of the sub-regions; and its scanty fauna has a general rather than any special resemblance to that of Africa. The entire destruction of its luxuriant native forests by the introduction of goats which killed all the young trees (a destruction which was nearly completed two centuries ago) must have led to the extermination of most of the indigenous birds and insects. At present there is no land bird that is believed to be really indigenous, and but one {270}wader, a small plover (_Ægialitis sanctæ-helenæ_) which is peculiar to the island, but closely allied to African species. Numerous imported birds, such as canaries, Java sparrows, some African finches, guinea-fowls, and partridges, are now wild. There are no native butterflies, but a few introduced species of almost world-wide range. The only important remnant of the original fauna consists of beetles and land shells. The beetles are the more numerous and have been critically examined and described by Mr. T. V. Wollaston, whose researches in the other Atlantic islands are so well known. _Coleoptera of St. Helena._--Omitting those beetles which get introduced everywhere through man's agency, there are 59 species of Coleoptera known from St. Helena; and even of these there are a few widely distributed species that may have been introduced by man. It will be well, therefore, to confine ourselves almost wholly to the species peculiar to the island, and, therefore, almost certainly forming part of the endemic or original fauna. Of these we find that 10 belong to genera which have a very wide range, and thus afford no indication of geographical affinity; 2 belong to genera which are characteristic of the Palæarctic fauna (_Bembidium_, _Longitarsus_); 3 to African genera (_Adoretus_, _Sciobius_, _Aspidomorpha_); and two species of _Calosoma_ are most allied to African species. There are also 4 African species, which may be indigenous in St. Helena. The peculiar genera, 7 in number, are, however, the most interesting. We have first _Haplothorax_, a large beetle allied to _Carabus_ and _Calosoma_, though of a peculiar type. This may be held to indicate a remote Palæarctic affinity. _Melissius_, one of the Dynastidæ, is allied to South African forms. _Microxylobius_, one of the Cossonides (a sub-family of Curculionidæ) is the most important genus, comprising as it does 13 species. It is, according to Mr. Wollaston, an altogether peculiar type, most allied to _Pentarthrum_, a genus found in St. Helena, Ascension, and the south of England, and itself very isolated. _Nesiotes_, another genus of Curculionidæ, belongs to a small group, the allied genera forming which inhabit Europe, Madeira, and Australia. A third peculiar and isolated genus is _Trachyphlæosoma_. The Anthribidæ are represented by {271}2 genera, _Notioxenus_ and _Homoeodera_, which are altogether peculiar and isolated, and contain 9 species. Thus no less than 27 species, or more than half of the undoubtedly indigenous beetles, belong to 5 peculiar and very remarkable genera of Rhyncophora. It appears from this enumeration, that the peculiar species as a whole, exhibit most affinity to the Ethiopian fauna; next to the South European fauna; and lastly to that of the islands of the North Atlantic; while there is such a large amount of peculiarity in the most characteristic forms, that no special geographical affinity can be pointed out. _Land Shells._--These consist of about a dozen living species, and about as many extinct found in the surface soil, and probably exterminated by the destruction of the forests. The genera are _Succinea_, _Zonites_, _Helix_, _Bulimus_, _Pupa_, and _Achatina_. The _Bulimi_ (all now extinct but one) comprise one large, and several small species, of a peculiar type, most resembling forms now inhabiting South America and the islands of the Pacific. _Zonites_ is chiefly South European, but the other genera are of wide range, and none are peculiar to the island. The marine shells are mostly Mediterranean, or West Indian species, with some found in the Indian Ocean; only 4 or 5 species being peculiar to the island. _Tristan d'Acunha._--This small island is situated nearly midway between the Cape of Good Hope and the mouth of the La Plata, but it is rather nearer Africa than America, and a little nearer still to St. Helena. An island so truly oceanic and of whose productions so little is known, cannot be placed in any region, and is only noticed here because it comes naturally after St. Helena. It is known to possess three peculiar land birds. One is a thrush (_Nesocichla eremita_) whose exact affinities are not determined; the other a small water-hen (_Gallinula nesiotis_) allied to our native species, but with shorter and softer wings, which the bird does not use for flight. A finch of the genus _Crithagra_ shows African affinities; while another recently described as _Nesospiza acunhæ_ (Journ. für Orn. 1873, p. 154) forms a new genus said to resemble more nearly some American forms. {272}The only known land-shells are 2 peculiar species of _Balea,_ a genus only found elsewhere in Europe and Brazil. _IV. Madagascar and the Mascarene Islands, or the Malagasy Sub-region._ This insular sub-region is one of the most remarkable zoological districts on the globe, bearing a similar relation to Africa as the Antilles to tropical America, or New Zealand to Australia, but possessing a much richer fauna than either of these, and in some respects a more remarkable one even than New Zealand. It comprises, besides Madagascar, the islands of Mauritius, Bourbon, and Rodriguez, the Seychelles and Comoro islands. Madagascar itself is an island of the first class, being a thousand miles long and about 250 miles in average width. It lies parallel to the coast of Africa, near the southern tropic, and is separated by 230 miles of sea from the nearest part of the continent, although a bank of soundings projecting from its western coast reduces this distance to about 160 miles. Madagascar is a mountainous island, and the greater part of the interior consists of open elevated plateaus; but between these and the coast there intervene broad belts of luxuriant tropical forests. It is this forest-district which has yielded most of those remarkable types of animal life which we shall have to enumerate; and it is probable that many more remain to be discovered. As all the main features of this sub-region are developed in Madagascar, we shall first endeavour to give a complete outline of the fauna of that country, and afterwards show how far the surrounding islands partake of its peculiarities. _Mammalia._--The fauna of Madagascar is tolerably rich in genera and species of mammalia, although these belong to a very limited number of families and orders. It is especially characterized by its abundance of Lemuridæ and Insectivora; it also possesses a few peculiar Carnivora of small size; but most of the other groups in which Africa is especially rich--apes and monkeys, lions, leopards and hyænas, zebras, giraffes, antelopes, elephants and rhinoceroses, and even porcupines and squirrels, are wholly wanting. No less than 40 distinct families of land {273}mammals are represented on the continent of Africa, only 11 of which occur in Madagascar, which also possesses 3 families peculiar to itself. The following is a list of all the genera of Mammalia as yet known to inhabit the island:-- PRIMATES. LEMURIDÆ. Indrisinæ. Species. _Indris_ 6 Lemurinæ. _Lemur_ 15 _Hapalemur_ 2 _Microcebus_ 4 _Chirogaleus_ 5 _Lepilemur_ 2 CHIROMYIDÆ. _Chiromys_ 1 BATS--(Chiroptera). PTEROPIDÆ. Pteropus 2 RHINOLOPHIDÆ. Rhinolophus 1 VESPERTILIONIDÆ. Vespertilio 1 Taphozous 1 NOCTILIONIDÆ. Nyctinomus 1 INSECTIVORA. CENTETIDÆ. _Centetes_ 2 _Hemicentetes_ 2 _Ericulus_ 2 _Oryzorictes_ 1 _Echinops_ 3 SORICIDÆ. Sorex 1 CARNIVORA. CRYPTOPROCTIDÆ. _Cryptoprocta_ 1 VIVERRIDÆ. _Fossa_ 2 _Galidia_ 3 _Galidictis_ 2 _Eupleres_ 1 UNGULATA. SUIDÆ. Potamochoerus 1 RODENTIA. MURIDÆ. _Nesomys_ 1 _Hypogeomys_ 1 _Brachytarsomys_ 1 We have here a total of 12 families, 27 genera, and 65 species of Mammals; 3 of the families and 20 of the genera (indicated by italics) being peculiar. All the species are peculiar, except perhaps one or two of the wandering bats. Remains of a _Hippopotamus_ have been found in a sub-fossil condition, showing that this animal probably inhabited the island at a not very remote epoch. The assemblage of animals above noted is remarkable, and seems to indicate a very ancient connection with the southern portion of Africa, before the apes, ungulates, and felines had entered it. The lemurs, which are here so largely developed, are {274}represented by a single group in Africa, with two peculiar forms on the West coast. They also re-appear under peculiar and isolated forms in Southern India and Malaya, and are evidently but the remains of a once wide-spread group, since in Eocene times they inhabited North America and Europe, and very probably the whole northern hemisphere. The Insectivora are another group of high antiquity, widely scattered over the globe under a number of peculiar forms; but in no equally limited area represented by so many peculiar types as in Madagascar. South and West Africa are also rich in this order. The Carnivora of Madagascar are mostly peculiar forms of Viverridæ, or civets, a family now almost confined to the Ethiopian and Oriental regions, but which was abundant in Europe during the Miocene period. The _Potamochoerus_ is a peculiar _species_ only, which may be perhaps explained by the unusual swimming powers of swine, and the semi-aquatic habits of this genus, leading to an immigration at a later period than in the case of the other Mammalia. The same remark will apply to the small _Hippopotamus_, which was coeval with the great Struthious bird Æpiornis. Rodents are only represented by three peculiar forms of Muridæ, but it is probable that others remain to be discovered. _Birds._--Madagascar is exceedingly rich in birds, and especially in remarkable forms of Passeres. No less than 88 genera and 111 species of land-birds have been discovered, and every year some additions are being made to the list. The African families of Passeres are almost all represented, only two being absent--Paridæ and Fringillidæ, both very poorly represented in Africa itself. Among the Picariæ, however, the case is very different, no less than 7 families being absent, viz.--Picidæ, or woodpeckers; Indicatoridæ, or honey-guides; Megalæmidæ, or barbets; Musophagidæ, or plantain-eaters; Coliidæ, or colies; Bucerotidæ, or hornbills; and Irrisoridæ, or mockers. Three of these are peculiar to Africa, and all are well represented there, so that their absence from Madagascar is a very remarkable fact. The number of peculiar genera in Madagascar constitutes one of the main features of its ornithology, and many of these are so {275}isolated that it is very difficult to classify them, and they remain to this day a puzzle to ornithologists. In order to exhibit clearly the striking characteristics of the bird-fauna of this island, we shall first give a list of all the peculiar genera; another, of the genera of which the species only are peculiar; and, lastly, a list of the species which Madagascar possesses in common with the African continent. GENERA OF BIRDS PECULIAR TO MADAGASCAR, OR FOUND ELSEWHERE ONLY IN THE MASCARENE ISLANDS. SYLVIIDÆ. Species. 1. Bernieria 2 2. Ellisia 1 3. Mystacornis 1 4. Eroessa 1 5. Gervasia 1 TIMALIIDÆ. 6. Oxylabes 2 CINCLIDÆ(?). 7. Mesites 1 SITTIDÆ. 8. _Hypherpes_ 1 PYCNONOTIDÆ(?) 9. Tylas 1 ORIOLIDÆ. 10. Artamia 3 11. Cyanolanius 1 MUSCICAPIDÆ. 12. Newtonia 1 13. Pseudobias 1 LANIIDÆ. 14. Calicalicus(?) 1 15. Vanga 4 NECTARINIIDÆ. 16. Neodrepanis 1 HIRUNDINIDÆ. 17. Phedina 1 PLOCEIDÆ. 18. Nelicurvius 1 STURNIDÆ. 19. Euryceros(?) 1 20. Hartlaubia 1 21. Falculia 1 PAICTIDÆ. 22. Philepitta 1 CUCULIDÆ. 23. Coua 9 24. Cochlothraustes 1 LEPTOSOMIDÆ. 25. Leptosomus 1 CORACIIDÆ. 26. Atelornis 2 27. Brachypteracias 1 28. Geobiastes 1 PSITTACIDÆ. 29. Coracopsis 2 COLUMBIDÆ. 30. _Alectrænas_ 1 TETRAONIDÆ. 31. _Margaroperdix_ 1 FALCONIDÆ. 32. Nisoides 1 33. Eutriorchis 1 -- Total species of peculiar genera 50 ÆPYORNITHIDÆ(extinct). 34. Æpyornis 1 {276}ETHIOPIAN OR ORIENTAL GENERA WHICH ARE REPRESENTED IN MADAGASCAR BY PECULIAR SPECIES. TURDIDÆ. Species. 1. Bessonornis 1 SYLVIIDÆ. 2. Acrocephalus 1 3. _Copsychus (Or.)_ 1 4. Pratincola 1 PYCNONOTIDÆ. 5. _Hypsipetes (Or.)_ 1 6. Andropadus 1 CAMPEPHAGIDÆ. 7. Campephaga 1 DICRURIDÆ. 8. Dicrurus 1 MUSCICAPIDÆ. 9. Tchitrea 1 LANIIDÆ. 10. Laniarius 1 NECTARINIIDÆ. 11. Nectarinia 1 PLOCEIIDÆ. 12. Foudia 2 13. Hypargos 1 14. Spermestes 1 ALAUDIDÆ. 15. Mirafra 1 MOTACILLIDÆ. 16. Motacilla 1 CUCULIDÆ. 17. Ceuthmochares 1 18. Centropus 1 19. Cuculus 1 CORACIIDÆ. 20. Eurystomus 1 ALCEDINIDÆ. 21. Corythornis 1 22. Ispidina 1 UPUPIDÆ. 23. Upupa (?) 1 CAPRIMULGIDÆ. 24. Caprimulgus 1 CYPSELIDÆ. 25. Cypselus 2 26. Chætura 1 PSITTACIDÆ. 27. Poliopsitta 1 COLUMBIDÆ. 28. Treron 1 29. Columba 1 30. Turtur 1 PTEROCLIDÆ. 31. Pterocles 1 TETRAONIDÆ. 32. Francolinus 1 PHASIANIDÆ. 33. Numida 1 TURNICIDÆ. 34. Turnix 1 FALCONIDÆ. 35. Polyboroides 1 36. Circus 1 37. Astur 3 38. Accipiter 1 39. Buteo 1 40. Haliæetus 1 41. Pernis 1 42. Baza 1 43. Cerchneis 1 STRIGIDÆ. {277} 44. Athene 1 45. Scops 1 RALLIDÆ. 46. Rallus 3 47. Porzana 1 SCOLOPACIDÆ. 48. Gallinago 1 PLATALEIDÆ. 49. Ibis 1 PODICIPIDÆ. 50. Podiceps 1 -- Total peculiar species of Eth. } or Or. genera } 56 SPECIES OF BIRDS COMMON TO MADAGASCAR AND AFRICA OR ASIA. 1. Cisticola cursitans. 2. Corvus scapulatus. 3. Crithagra canicollis. 4. Merops superciliosus. 5. Collocalia fuciphaga. 6. Oena capensis. 7. Aplopelia tympanistria. 8. Falco minor. 9. Falco concolor. 10. Milvus ægyptius. 11. Milvus migrans. 12. Strix flammea. These three tables show us an amount of speciality hardly to be found in the birds of any other part of the globe. Out of 111 land-birds in Madagascar, only 12 are identical with species inhabiting the adjacent continents, and most of these belong to powerful-winged, or wide-ranging forms, which probably now often pass from one country to the other. The peculiar species--49 land-birds and 7 waders, or aquatics--are mostly well-marked forms of African genera. There are, however, several genera (marked by italics) which have Oriental or Palæarctic affinities, but not African, viz.--_Copsychus_, _Hypsipetes_, _Hypherpes_, _Alectrænas_, and _Margaroperdix_. These indicate a closer approximation to the Malay countries than now exists. The table of 33 peculiar genera is of great interest. Most of these are well-marked forms, belonging to families which are fully developed in Africa; though it is singular that not one of the exclusively African families is represented in any way in Madagascar. Others, however, are of remote or altogether doubtful affinities. _Sittidæ_ is Oriental and Palæarctic, but not Ethiopian. _Oxylabes_ and _Mystacornis_ are of doubtful affinities. _Artamia_ and _Cyanolanius_ still more so, and it is quite undecided what family they belong to. _Calicalicus_ is almost equally obscure. _Neodrepanis_, one of the most recent discoveries, seems to connect the Nectariniidæ with the Pacific {278}Depanididæ. _Euryceros_ is a complete puzzle, having been placed with the hornbills, the starlings, or as a distinct family. _Falculia_ is an exceedingly aberrant form of starling, long thought to be allied to _Irrisor_. _Philepitta_, forming a distinct family, (Paictidæ), is most remarkable and isolated, perhaps with remote South American affinities. _Leptosoma_ is another extraordinary form, connecting the cuckoos with the rollers. _Atelornis_, _Brachypteracias_, and _Geobiastes_, are terrestrial rollers, with the form and colouring of _Pitta_. So many perfectly isolated and remarkable groups are certainly nowhere else to be found; and they fitly associate with the wonderful aye-aye (_Chiromys_), the insectivorous Centetidæ, and carnivorous _Cryptoprocta_ among the Mammalia. They speak to us plainly of enormous antiquity, of long-continued isolation; and not less plainly of a lost continent or continental island, in which so many, and various, and peculiarly organized creatures, could have been gradually developed in a connected fauna, of which we have here but the fragmentary remains. _Plate VI.--Illustrating the characteristic features of the Zoology of Madagascar._--The lemurs, which form the most prominent feature in the zoology of Madagascar, being comparatively well-known from the numerous specimens in our zoological gardens; and good figures of the Insectivorous genera not being available, we have represented the nocturnal and extraordinary aye-aye (_Chiromys madagascariensis_) to illustrate its peculiar and probably very ancient mammalian fauna; while the river-hogs in the distance (_Potamochoerus edwardsii_) allied to African species, indicate a later immigration from the mainland than in the case of most of the other Mammalia. The peculiar birds being far less generally known, we have figured three of them. The largest is the _Euryceros prevosti_, here classed with the starlings, although its remarkable bill and other peculiarities render it probable that it should form a distinct family. Its colours are velvety black and rich brown with the bill of a pearly grey. The bird beneath (_Vanga curvirostris_) is one of the peculiar Madagascar shrikes whose plumage, variegated with green-black and pure white is very conspicuous; while that in the right hand corner is the _Leptosoma discolor_, a bird which appears to be intermediate between such very distinct families as the cuckoos and the rollers, and is therefore considered to form a family by itself. It is a coppery-green above and nearly white beneath, with a black bill and red feet. The fan-shaped plant on the left is the traveller's tree (_Urania speciosa_), one of the peculiar forms of vegetation in this marvellous island. Plate VI. [Illustration] SCENE IN MADAGASCAR, WITH CHARACTERISTIC ANIMALS. {279}_Reptiles._--These present some very curious features, comparatively few of the African groups being represented, while there are a considerable number of Eastern and even of American forms. Beginning with the snakes, we find, in the enormous family of Colubridæ, none of the African types; but instead of them three genera--_Herpetodryas_, _Philodryas_, and _Heterodon_--only found elsewhere in South and North America. The Psammophidæ, which are both African and Indian, are represented by a peculiar genus, _Mimophis_. The Dendrophidæ are represented by _Ahætulla_, a genus which is both African and American. The Dryiophidæ, which inhabit all the tropics but are most developed in the Oriental region, are represented by a peculiar genus, _Langaha_. The tropical Pythonidæ are represented by another peculiar genus, _Sanzinia_. The Lycodontidæ and Viperidæ, so well developed in Africa, are entirely absent. The lizards are no less remarkable. The Zonuridæ, abundantly developed in Africa, are represented by one peculiar genus, _Cicigna_. The wide-spread Scincidæ by another peculiar genus, _Pygomeles_. The African Sepsidæ, are represented by three genera, two of which are African, and one, _Amphiglossus_, peculiar. The Acontiadæ are represented by a species of the African genus _Acontias_. Of Scincidæ there is the wide-spread _Euprepes_. The Sepidæ are represented by the African genera _Seps_ and _Scelotes_. The Geckotidæ are not represented by any purely African genera, but by _Phyllodactylus_, which is American and Australian; _Hemidactylus_, which is spread over all the tropics; by two peculiar genera; and by _Uroplatis_, _Geckolepis_, and _Phelsuma_, confined to Madagascar, Bourbon, and the Andaman Islands. The Agamidæ, which are mostly Oriental and are represented in {280}Africa by the single genus _Agama_, have here three peculiar genera, _Tracheloptychus_, _Chalarodon_, and _Hoplurus_. Lastly, the American Iguanidæ are said to be represented by a species of the South American genus _Oplurus_. The classification of Reptiles is in such an unsettled state that some of these determinations of affinities are probably erroneous; but it is not likely that any corrections which may be required will materially affect the general bearing of the evidence, as indicating a remarkable amount of Oriental and American relationship. The other groups are of less interest. Tortoises are represented by two African or wide-spread genera of Testudinidæ, _Testudo_ and _Chersina_, and by one peculiar genus, _Pyxis_; and there are also two African genera of Chelydidæ. The Amphibia are not very well known. They appear to be confined to species of the wide-spread Ethiopian and Oriental genera--_Hylarana_, _Polypedates_, and _Rappia_ (Polypedatidæ); and _Pyxicephalus_ (Ranidæ). _Fresh-water Fishes._--These appear to be at present almost unknown. When carefully collected they will no doubt furnish some important facts. _The Mascarene Islands._ The various islands which surround Madagascar--Bourbon, Mauritius, Rodriguez, the Seychelles, and the Comoro Islands--all partake in a considerable degree of its peculiar fauna, while having some special features of their own. Indigenous Mammalia (except bats) are probably absent from all these islands (except the Comoros), although _Lemur_ and _Centetes_ are given as natives of Bourbon and Mauritius. They have, however, perhaps been introduced from Madagascar. _Lemur mayottensis_, a peculiar species, is found in the Comoro Islands, where a Madagascar species of _Viverra_ also occurs. Bourbon and Mauritius may be taken together, as they much resemble each other. They each possess species of a peculiar genus of Campephagidæ, or caterpillar shrikes, _Oxynotus_; while the remarkable _Fregilupus_, belonging to the starling family, inhabits Bourbon, if it is not now extinct. They also have {281}peculiar species of _Pratincola_, _Hypsipetes_, _Phedina_, _Tchitrea_, _Zosterops_, _Foudia_, _Collocalia_, and _Coracopsis_; while Mauritius has a very peculiar form of dove of the sub-genus _Trocaza_; an _Alectrænas_, extinct within the last thirty years; and a species of the Oriental genus of parroquets, _Palæornis_. The small and remote island of Rodriguez has another _Palæornis_, as well as a peculiar _Foudia_, and a _Drymoeca_ of apparently Indian affinity. Coming to the Seychelle Islands, far to the north, we find the only mammal an Indian species of bat (_Pteropus edwardsii_). Of the twelve land-birds all but one are peculiar species, but all belong to genera found also in Madagascar, except one--a peculiar species of _Palæornis_. This is an Oriental genus, but found also in several Mascarene Islands and on the African continent. A species of black parrot (_Coracopsis barklayi_) and a weaver bird of peculiar type (_Foudia seychellarum_) show, however, a decided connection with Madagascar. There are also two peculiar pigeons--a short-winged _Turtur_ and an _Alectrænas_. Most of the birds of the Comoro Islands are Madagascar species, only two being African. Five are peculiar, belonging to the genera _Nectarinia_, _Zosterops_, _Dicrurus_, _Foudia_, and _Alectrænas_. Reptiles are scarce. There appear to be no snakes in Mauritius and Bourbon, though some African species are said to be found in the Seychelle Islands. Lizards are fairly represented. Mauritius has _Cryptoblepharus_, an Australian genus of Gymnopthalmidæ; _Hemidactylus_ (a wide-spread genus); _Peropus_ (Oriental and Australian)--both belonging to the Geckotidæ. Bourbon has _Heteropus_, a Moluccan and Australian genus of Scincidæ; _Phelsuma_ (Geckotidæ), and _Chameleo_, both found also in Madagascar; as well as _Pyxis_, one of the tortoises. The Seychelles have _Theconyx_, a peculiar genus of Geckotidæ, and _Chameleo_. Gigantic land-tortoises, which formerly inhabited most of the Mascarene Islands, now only survive in Aldabra, a small island north of the Seychelles. These will be noticed again further on. Amphibia seem only to be recorded from the Seychelles, where two genera of tree-frogs of the family Polypedatidæ are found; one (_Megalixalus_) peculiar, the other (_Rappia_) found also in Madagascar and Africa. {282}The few insect groups peculiar to these islands will be noted when we deal with the entomology of Madagascar. _Extinct fauna of the Mascarene Islands and Madagascar._--Before quitting the vertebrate groups, we must notice the remarkable birds which have become extinct in these islands little more than a century ago. The most celebrated is the dodo of the Mauritius (_Didus ineptus_), but an allied genus, _Pezophaps_, inhabited Rodriguez, and of both of these almost perfect skeletons have been recovered. Other species probably existed in Bourbon. Remains of two genera of flightless rails have also been found, _Aphanapteryx_ and _Erythromachus_; and even a heron (_Ardea megacephala_) which was short-winged and seldom flew; while in Madagascar there lived a gigantic Struthious bird, the _Æpyornis_. Some further details as to these extinct forms will be found under the respective families, Dididæ, Rallidæ, and Æpyornithidæ, in the fourth part of this work; and their bearing on the past history of the region will be adverted to in the latter part of this chapter. Dr. Günther has recently distinguished five species of fossil tortoises from Mauritius and Rodriguez,--all of them quite different from the living species of Aldabra. _Insects._--The butterflies of Madagascar are not so remarkable as some other orders of insects. There seems to be only one peculiar genus, _Heteropsis_ (Satyridæ). The other genera are African, _Leptoneura_ being confined to Madagascar and South Africa. There are some fine _Papilios_ of uncommon forms. The most interesting lepidopterous insect, however, is the fine diurnal moth (_Urania_), as all the other species of the genus inhabit tropical America and the West Indian Islands. The Coleoptera have been better collected, and exhibit some very remarkable affinities. There is but one peculiar genus of Cicindelidæ, _Pogonostoma_, which is allied to the South American genus, _Ctenostoma_. Another genus, _Peridexia_, is common to Madagascar and South America. None of the important African genera are represented, except _Eurymorpha_; while _Meglaomma_ is common to Madagascar and the Oriental region. In the Carabidæ we have somewhat similar phenomena on a {283}wider scale. Such large and important African genera as _Polyhirma_ and _Anthia_, are absent; but there are four genera in common with South Africa, and two with West Africa; while three others are as much Oriental as African. One genus, _Distrigus_, is wholly Oriental; and another, _Homalosoma_, Australian. _Colpodes_, well developed in Bourbon and Mauritius, is Oriental and South American. Of the peculiar genera, _Sphærostylis_ has South American affinities; _Microchila_, Oriental; the others being related to widely distributed genera. The Lucanidæ are few in number, and all have African affinities. Madagascar is very rich in Cetoniidæ, and possesses 20 peculiar genera. _Bothrorhina_, and three other genera belonging to the _Ichnostoma_ group, have wholly African relations. _Doryscelis_ and _Chromoptila_ are no less clearly allied to Oriental genera. A series of eight peculiar genera belong to the Schizorhinidæ, a family the bulk of which are Australian, while there are only a few African forms. The remaining genera appear to have African affinities, but few of the peculiarly African genera are represented. _Glyciphana_ is characteristic of the Oriental region. The Buprestidæ of Madagascar consist mainly of one large and peculiar genus, _Polybothris_, allied to the almost cosmopolite _Psiloptera_. Most of the other genera are both Ethiopian and Oriental; but _Polycesta_ is mainly South American, and the remarkable and isolated genus _Sponsor_ is confined to the Mauritius with a species in Celebes and New Guinea. The Longicorns are numerous and interesting, there being no less than 24 peculiar genera. Two of the genera of Prionidæ are very isolated, while a third, _Closterus_, belongs to a group which is Malayan and American. Of the Cerambycidæ, _Philematium_ ranges to Africa and the West Indies; _Leptocera_ is only found eastward in Ceylon and the New Hebrides; while _Euporus_ is African. Of the peculiar genera, 2 are of African type; 3 belong to the _Leptura_ group, which are mostly Palæarctic and Oriental, with a few in South Africa; while _Philocalocera_ is allied to a South American genus. Among the Lamiidæ there are several wide-ranging and 7 {284}African genera; but _Coptops_ is Oriental, and the Oriental _Praonetha_ occurs in the Comoro Islands. Among the peculiar genera several have African affinities, but _Tropidema_ belongs to a group which is Oriental and Australian; _Oopsis_ is found also in the Pacific Islands; _Mythergates_, _Sulemus_, and _Coedomæa_, are allied to Malayan and American genera. _General Remarks on the Insect-fauna of Madagascar._--Taking the insects as a whole, we find the remarkable result that their affinities are largely Oriental, Australian, and South American: while the African element is represented chiefly by special South African or West African forms, rather than by such as are widely spread over the Ethiopian region.[11] In some families--as Cetoniidæ and Lamiidæ--the African element appears to preponderate; in others--as Cicindelidæ--the South American affinity seems strongest; in Carabidæ, perhaps the Oriental; while in Buprestidæ and Cerambycidæ the African and foreign elements seem nearly balanced. We must not impute too much importance to these foreign alliances among insects, because we find examples of them in every country on the globe. The reason they are so much more pronounced in Madagascar may be, that during long periods of time this island has served as a refuge for groups that have been dying out on the great continents; and that, owing to the numerous deficiencies of a somewhat similar kind in the series of vertebrata in Australia and South America, the same groups have often been able to maintain themselves in all these countries as well as in Madagascar. It must be remembered too, that these peculiarities in the Malagasy and Mascarene insect-fauna are but exaggerations of a like phenomenon on the mainland. Africa also has numerous affinities with South America, with the Malay countries, and with Australia; but they do not bear anything like so large a proportion to the whole fauna, and do not, therefore, attract so much attention. The special conditions of existence and the long-continued isolation of Madagascar, will account for much of this difference; and it will evidently not be necessary {285}to introduce, as some writers are disposed to do, a special land connection or near approach between Madagascar and all these countries, independently of Africa; except perhaps in the case of the Malay Islands, as will be discussed further on. _Land-shells._--Madagascar and the adjacent islands are all rich in land-shells. The genera of Helicidæ are _Vitrina_, _Helix_, _Achatina_, _Columna_ (peculiar to Madagascar and West Africa), _Buliminus_, _Cionella_ (chiefly Oriental and South American, but not African), _Pupa_, _Streptaxis_, and _Succinea_. Among the Operculata we have _Truncatella_ (widely scattered, but not African); _Cyclotus_ (South American, Oriental, and South African); _Cyclophorus_ (mostly Oriental, with a few South African); _Leptopoma_ (Oriental); _Megalomastoma_ (Malayan and South American); _Lithidion_ (peculiar to Madagascar, Socotra, and South-West Arabia); _Otopoma_ (with the same range, but extending to West India and New Ireland); _Cyclostomus_ (widely spread but not African); and _Omphalotropis_ (wholly Oriental and Australian). We thus find the same general features reproduced in the land-shells as in the insects, and the same remarks will to a great extent apply to both. The classification of the former is, however, by no means so satisfactory, and we have no extensive and accurate general catalogues of shells, like those of Lepidoptera and Coleoptera, which have furnished us with such valuable materials for the comparison of the several faunas. _On the probable Past History of the Ethiopian Region._ Perhaps none of the great zoological regions of the earth present us with problems of greater difficulty or higher interest than the Ethiopian. We find in it the evidence of several distinct and successive faunas, now intermingled; and it is very difficult, with our present imperfect knowledge, to form an adequate conception of how and when the several changes occurred. There are, however, a few points which seem sufficiently clear, and these afford us a secure foundation in our endeavour to comprehend the rest. Let us then consider what are the main facts we have to account for.--1. In Continental Africa, more especially in the south {286}and west, we find, along with much that is peculiar, a number of genera showing a decided Oriental, and others with an equally strong South American affinity; this latter more particularly showing itself among reptiles and insects. 2. All over Africa, but more especially in the east, we have abundance of large ungulates and felines--antelopes, giraffes, buffaloes, elephants, and rhinoceroses, with lions, leopards, and hyænas, all of types now or recently found in India and Western Asia. 3. But we also have to note the absence of a number of groups which abound in the above-named countries, such as deer, bears, moles, and true pigs; while camels and goats--characteristic of the desert regions just to the north of the Ethiopian--are equally wanting. 4. There is a wonderful unity of type and want of speciality in the vast area of our first sub-region extending from Senegal across to the east coast, and southward to the Zambezi; while West Africa and South Africa each abound in peculiar types. 5. We have the extraordinary fauna of Madagascar to account for, with its evident main derivation from Africa, yet wanting all the larger and higher African forms; its resemblances to Malaya and to South America; and its wonderful assemblage of altogether peculiar types. Here we find a secure starting-point, for we are sure that Madagascar must have been separated from Africa before the assemblage of large animals enumerated above, had entered it. Now, it is a suggestive fact, that all these belong to types which abounded in Europe and India about the Miocene period. It is also known, from the prevalence of Tertiary deposits over the Sahara and much of Arabia, Persia, and Northern India, that during early Tertiary times a continuous sea from the Bay of Bengal to the British Isles completely cut off all land communication between Central and Southern Africa on the one side, and the great continent of the Eastern hemisphere on the other. When Africa was thus isolated, its fauna probably had a character somewhat analogous to that of South America at the same period. Most of the higher types of mammalian life were absent, while lemurs, Edentates, and Insectivora took their place. At this period Madagascar was no doubt united with Africa, {287}and helped to form a great southern continent which must at one time have extended eastward as far as Southern India and Ceylon; and over the whole of this the lemurine type no doubt prevailed. During some portion of this period, South Temperate Africa must have had a much greater extension, perhaps indicated by the numerous shoals and rocks to the south and east of the Cape of Good Hope, and by the Crozets and Kerguelen Islands further to the south-east. This would have afforded means for that intercommunion with Western Australia which is so clearly marked in the flora, and to some extent also in the insects of the two countries; and some such extension is absolutely required for the development of that wonderfully rich and peculiar temperate flora and fauna, which, now crowded into a narrow territory, is one of the greatest marvels of the organic world. During this early period, when the great southern continents--South America, Africa, and Australia--were equally free from the incursions of the destructive felines of the north, the Struthious or ostrich type of birds was probably developed into its existing forms. It is not at all necessary to suppose that these three continents were at any time united, in order to account for the distribution of these great terrestrial birds; as this may have arisen by at least two other easily conceivable modes. The ancestral Struthious type may, like the Marsupial, have once spread over the larger portion of the globe; but as higher forms, especially of Carnivora, became developed, it would be exterminated everywhere but in those regions where it was free from their attacks. In each of these it would develope into special forms adapted to surrounding conditions; and the large size, great strength, and excessive speed of the ostrich, may have been a comparatively late development caused by its exposure to the attacks of enemies which rendered such modification necessary. This seems the most probable explanation of the distribution of Struthious birds, and it is rendered almost certain by the discovery of remains of this order in Europe in Eocene deposits, and by the occurrence of an ostrich among the fossils of the Siwalik hills; but it is just possible, also, that the {288}ancestral type may have been a bird capable of flight, and that it spread from one of the three southern continents to the others at the period of their near approach, and more or less completely lost the power of flight owing to the long continued absence of enemies. During the period we have been considering, the ancestors of existing apes and monkeys flourished (as we have seen in Chapter VI.) along the whole southern shores of the old Palæarctic continent; and it seems likely that they first entered Africa by means of a land connection indicated by the extensive and lofty plateaus of the Sahara, situated to the south-east of Tunis and reaching to a little north-west of Lake Tchad; and at the same time the elephant and rhinoceros type may have entered. This will account for the curious similarity between the higher faunas of West Africa and the Indo-Malay sub-region, for owing to the present distribution of land and sea and the narrowing of the tropical zone since Miocene times, these are now the only lowland, equatorial, forest-clad countries, which were in connection with the southern shores of the old Palæarctic continent at the time of its greatest luxuriance and development. This western connection did not probably last long, the junction that led to the greatest incursion of new forms, and the complete change in the character of the African fauna, having apparently been effected by way of Syria and the shores of the Red Sea at a somewhat later date. By this route the old South-Palæarctic fauna, indicated by the fossils of Pikermi and the Siwalik Hills, poured into Africa; and finding there a new and favourable country, almost wholly unoccupied by large Mammalia, increased to an enormous extent, developed into new forms, and finally overran the whole continent. Before this occurred, however, a great change had taken place in the geography of Africa. It had gradually diminished on the south and east; Madagascar had been left isolated; while a number of small islands, banks, and coral reefs in the Indian Ocean alone remained to indicate the position of a once extensive equatorial land. The Mascarene Islands appear to represent the portion which separated earliest, before any carnivora had {289}reached the country; and it was in consequence of this total exemption from danger, that several groups of birds altogether incapable of flight became developed here, culminating in the huge and unwieldy Dodo, and the more active Aphanapteryx. To the same cause may be attributed the development, in these islands, of gigantic land-tortoises, far surpassing any others now living on the globe. They appear to have formerly inhabited Mauritius, Bourbon, and Rodriguez, and perhaps all the other Mascarene islands, but having been recklessly destroyed, now only survive in the small uninhabited Aldabra islands north of the Seychelle group. The largest living specimen (5½ feet long) is now in our Zoological Gardens. The only other place where equally large tortoises (of an allied species) are found, is the Galapagos islands, where they were equally free from enemies till civilized man came upon the scene; who, partly by using them for food, partly by the introduction of pigs, which destroy the eggs, has greatly diminished their numbers and size, and will probably soon wholly exterminate them. It is a curious fact, ascertained by Dr. Günther, that the tortoises of the Galapagos are more nearly related to the extinct tortoises of Mauritius than is the living tortoise of Aldabra. This would imply that several distinct groups or sub-genera of _Testudo_ have had a wide range over the globe, and that some of each have survived in very distant localities. This is rendered quite conceivable by the known antiquity of the genus _Testudo_, which dates back to at least the Eocene formation (in North America) with very little change of form. These sluggish reptiles, so long-lived and so tenacious of life, may have remained unchanged, while every higher animal type around them has become extinct and been replaced by very different forms; as in the case of the living _Emys tectum_, which is the sole survivor of the strange Siwalik fauna of the Miocene epoch. The ascertained history of the genus and the group, thus affords a satisfactory explanation of the close affinity of the gigantic tortoises of Mauritius and the Galapagos. The great island of Madagascar seems to have remained longer united with Africa, till some of the smaller and more active {290}carnivora had reached it; and we consequently find there, no wholly terrestrial form of bird but the gigantic and powerful _Æpyornis_, well able to defend itself against such enemies. As already intimated, we refer the South American element in Madagascar, not to any special connection of the two countries independently of Africa, but to the preservation there of a number of forms, some derived from America through Africa, others of once almost cosmopolitan range, but which, owing to the severer competition, have become extinct on the African continent, while they have continued to exist under modified forms in the two other countries. The depths of all the great oceans are now known to be so profound, that we cannot conceive the elevation of their beds above the surface without some corresponding depression elsewhere. And if, as is probable, these opposite motions of the earth's crust usually take place in parallel bands, and are to some extent dependent on each other, an elevation of the sea bed could hardly fail to lead to the submergence of large tracts of existing continents; and this is the more likely to occur on account of the great disproportion that we have seen exists between the mean height of the land and the mean depth of the ocean. Keeping this principle in view, we may, with some probability, suggest the successive stages by which the Ethiopian region assumed its present form, and acquired the striking peculiarities that characterise its several sub-regions. During the early period, when the rich and varied temperate flora of the Cape, and its hardly less peculiar forms of insects and of low type mammalia, were in process of development in an extensive south temperate land, we may be pretty sure that the whole of the east and much of the north of Africa was deep sea. At a later period, when this continent sank towards the south and east, the elevation may have occurred which connected Madagascar with Ceylon; and only at a still later epoch, when the Indian Ocean had again been formed, did central, eastern, and northern Africa gradually rise above the ocean, and effect a connection with the great northern continent by way of Abyssinia and Arabia. And if this last change took place with {291}tolerable rapidity, or if the elevatory force acted from the north towards the south, there would be a new and unoccupied territory to be taken possession of by immigrants from the north, together with a few from the south and west. The more highly-organised types from the great northern continent, however, would inevitably prevail; and we should thus have explained the curious uniformity in the fauna of so large an area, together with the absence from it of those peculiar Ethiopian types which so abundantly characterise the other three sub-regions. We may now perhaps see the reason of the singular absence from tropical Africa of deer and bears; for these are both groups which live in fertile or well-wooded countries, whereas the line of immigration from Europe to Africa was probably always, as now, to a great extent a dry and desert tract, suited to antelopes and large felines, but almost impassable to deer and bears. We find, too, that whereas remains of antelopes and giraffes abound in the Miocene deposits of Greece, there were no deer (which are perhaps a somewhat later development); neither were there any bears, but numerous forms of Felidæ, Viverridæ, Mustelidæ, and ancestral forms of _Hyæna_, exactly suited to be the progenitors of the most prevalent types of modern African Zoology. There appears to have been one other change in the geography of Africa and the Atlantic Ocean that requires notice. The rather numerous cases of close similarity in the insect forms of tropical Africa and America, seem to indicate some better means of transmission, at a not very remote epoch, than now exists. The vast depth of the Atlantic, and the absence of any corresponding likeness in the vertebrate fauna, entirely negative the idea of any union between the two countries; but a moderate extension of their shores towards each other is not improbable, and this, with large islands in the place of the Cape Verd group, St. Paul's Rocks, and Fernando Noronha, to afford resting places in the Atlantic, would probably suffice to explain the amount of similarity that actually exists. Our knowledge of the geology and palæontology of Africa {292}being so scanty, it would be imprudent to attempt any more detailed explanation of the peculiarities of its existing fauna. The sketch now given is, it is believed, founded on a sufficient basis of facts to render it not only a possible but a probable account of what took place; and it is something gained to be able to show, that a large portion of the peculiarities and anomalies of so remarkable a fauna as that of the Ethiopian region, can be accounted for by a series of changes of physical geography during the tertiary epoch, which can hardly be considered extreme, or in any way unlikely to have occurred. {293}TABLES OF DISTRIBUTION. In drawing up these tables showing the distribution of various classes of animals in the Ethiopian Region, the following sources of information have been chiefly relied on, in addition to the general treatises, monographs, and catalogues, used for the Fourth Part of this work:-- _Mammalia._--Blanford's Abyssinia; Peters's Mozambique; Heuglin and Schweinfurth for North East Africa; Grandidier Schlegel, &c., for Madagascar; the local lists given by Mr. Andrew Murray; numerous papers by Fraser, Gray, Kirk, Mivart, Peters, Sclater, and Speke; and a MS. list of Bovidæ from Sir Victor Brooke. _Birds._--Finsch and Hartlaub for East Africa; Heuglin for North-East Africa; Blanford for Abyssinia; Layard for South Africa; Hartlaub for West Africa; Dohrn for Princes Island; Andersson for Damaraland; and papers by Gurney, Hartlaub, Kirk, Newton, Peters, Sharpe, Sclater, Schlegel, and Pollen and a MS. list of Madagascar Birds from Mr. Sharpe. {294}TABLE I. _FAMILIES OF ANIMALS INHABITING THE ETHIOPIAN REGION._ EXPLANATION. Names in _italics_ show families peculiar to the region. Names inclosed thus (......) barely enter the region, and are not considered properly to belong to it. Numbers are not consecutive, but correspond to those in Part IV. ---------------------+-------------------+------------------------------- | Sub-regions | | 1=East Africa. | Order and Family | 2=West Africa. | Range beyond the Region. | 3=South Africa. | | 4=Madagascar. | ---------------------+----+----+----+----+------------------------------- | 1. | 2. | 3. | 4. | ---------------------+----+----+----+----+------------------------------- | | | | | MAMMALIA. | | | | | PRIMATES. | | | | | 1. Simiidæ | | -- | | |Oriental 2. Semnopithecidæ | -- | -- | | |Oriental 3. Cynopithecidæ | -- | -- | -- | |Oriental, Palæarctic 6. Lemuridæ | -- | -- | -- | -- |Oriental 8. _Chiromyidæ_ | | | | -- | | | | | | CHEIROPTERA. | | | | | 9. Pteropidæ | -- | -- | -- | -- |Oriental, Australian 11. Rhinolophidæ | -- | -- | -- | -- |The Eastern Hemisphere 12. Vespertilionidæ | -- | -- | -- | -- |Cosmopolite 13. Noctilionidæ | -- | -- | -- | -- |All Tropical regions | | | | | INSECTIVORA. | | | | | 15. Macroscelididæ | -- | | -- | |South Palæarctic 17. Erinaceidæ | | | -- | |Palæarctic, Oriental 18. _Centetidæ_ | | | | -- |Greater Antilles 19. _Potamogalidæ_ | | -- | | | 20. _Chrysochloridæ_ | -- | | -- | | 22. Soricidæ | -- | -- | -- | -- |All regions but Australian and | | | | | Neotropical | | | | | CARNIVORA. | | | | | 23. Felidæ | -- | -- | -- | -- |All regions but Australian 24. _Cryptoproctidæ_ | | | | -- | 25. Viverridæ | -- | -- | -- | -- |Oriental, S. Palæarctic 26. _Protelidæ_ | | | -- | | 27. Hyænidæ | -- | -- | -- | |S. Palæarctic, India 28. Canidæ | -- | -- | -- | |Almost cosmopolite 29. Mustelidæ | -- | -- | -- | |All regions but Australian 33. Otariidæ | | | -- | |All temperate regions | | | | | CETACEA. | | | | | 36 to 41. | | | | |Oceanic | | | | | SIRENIA. | | | | | 42. Manatidæ | -- | -- | | |Neotropical, Oriental, | | | | | Australian | | | | | UNGULATA. | | | | | 43. Equidæ | -- | -- | -- | |Palæarctic 45. Rhinocerotidæ | -- | -- | -- | |Oriental 46. _Hippopotamidæ_ | -- | -- | -- | | 47. Suidæ | -- | -- | -- | -- |Cosmopolite; excl. Australia 49. Tragulidæ | | -- | | |Oriental 51. _Camelopardidæ_ | -- | | -- | | 52. Bovidæ | -- | -- | -- | |All regions but Neotrop. and | | | | | Australian | | | | | PROBOSCIDEA. | | | | | 53. Elephantidæ | -- | -- | -- | |Oriental | | | | | HYRACOIDEA. | | | | | 54. Hyracidæ | -- | -- | -- | |Syria | | | | | RODENTIA. | | | | | 55. Muridæ | -- | -- | -- | -- |Cosmopolite; excl. Oceania 56. Spalacidæ | -- | -- | -- | |Palæarctic, Oriental 57. Dipodidæ | -- | -- | -- | |Palæarctic, Nearctic 58. Myoxidæ | -- | -- | -- | |Palæarctic 61. Sciuridæ | -- | -- | -- | |All regions but Australian 64. Octodontidæ | -- | | | |N. Africa, Neotropical 65. Echimyidæ | -- | | -- | |Neotropical 67. Hystricidæ | -- | -- | -- | |S. Palæarctic, Oriental 70. Leporidæ | -- | | -- | |All regions but Australian | | | | | EDENTATA. | | | | | 72. Manididæ | -- | -- | -- | |Oriental 74. _Orycteropodidæ_ | -- | | -- | | | | | | | BIRDS. | | | | | PASSERES. | | | | | 1. Turdidæ | -- | -- | -- | -- |Almost Cosmopolite 2. Sylviidæ | -- | -- | -- | -- |Cosmopolite 3. Timaliidæ | -- | -- | -- | -- |Oriental, Australian 5. Cinclidæ? | | | | -- |Widely scattered 6. Troglodytidæ | -- | -- | -- | |Almost Cosmopolite 9. Sittidæ | | | | -- |Palæarctic, Oriental, | | | | | Australian 10. Paridæ | -- | -- | -- | |All regions but Australian 13. Pycnonotidæ | -- | -- | -- | -- |Oriental 14. Oriolidæ | -- | -- | -- | -- |Oriental, Australian 15. Campephagidæ | -- | -- | -- | -- |Oriental, Australian 16. Dicruridæ | -- | -- | -- | -- |Oriental, Australian 17. Muscicapidæ | -- | -- | -- | -- |The Eastern Hemisphere 19. Laniidæ | -- | -- | -- | -- |The Eastern Hemisphere and | | | | | North America 20. Corvidæ | -- | -- | -- | -- |Cosmopolite 23. Nectariniidæ | -- | -- | -- | -- |Oriental, Australian 24. Dicæidæ | -- | -- | -- | -- |Oriental, Australian 30. Hirundinidæ | -- | -- | -- | -- |Cosmopolite 33. Fringillidæ | -- | -- | -- | -- |Cosmopolite, except Australian | | | | | region 34. Ploceidæ | -- | -- | -- | -- |Oriental, Australian 35. Sturnidæ | -- | -- | -- | -- |Eastern Hemisphere 37. Alaudidæ | -- | -- | -- | -- |Eastern Hemisphere and North | | | | | America 38. Motacillidæ | -- | -- | -- | -- |The Eastern Hemisphere 47. Pittidæ | | -- | | |Oriental, Australian 48. _Paictidæ_ | | | | -- | | | | | | PICARIÆ. | | | | | 51. Picidæ | -- | -- | -- | |Cosmopolite, excl. Australian | | | | | region 52. Yungidæ | -- | | -- | |Palæarctic 53. Indicatoridæ | -- | -- | -- | |Oriental 54. Megalæmidæ | -- | -- | -- | |Oriental, Neotropical 56. _Musophagidæ_ | -- | -- | -- | | 57. _Coliidæ_ | -- | -- | -- | | 58. Cuculidæ | -- | -- | -- | -- |Cosmopolite 59. _Leptosomidæ_ | | | | -- | 62. Coraciidæ | -- | -- | -- | -- |Oriental, Australian 63. Meropidæ | -- | -- | -- | -- |Oriental, Australian 66. Trogonidæ | -- | -- | -- | |Oriental, Neotropical 67. Alcedinidæ | -- | -- | -- | -- |Cosmopolite 68. Bucerotidæ | -- | -- | -- | |Oriental and to N. Guinea 69. Upupidæ | -- | -- | -- | -- |Palæarctic, Oriental 70. _Irrisoridæ_ | -- | -- | -- | | 73. Caprimulgidæ | -- | -- | -- | -- |Cosmopolite 74. Cypselidæ | -- | -- | -- | -- |Almost Cosmopolite | | | | | PSITTACI. | | | | | 78. Palæornithidæ | -- | -- | | -- |Oriental 81. Psittacidæ | -- | -- | -- | -- |Neotropical | | | | | COLUMBÆ. | | | | | 84. Columbidæ | -- | -- | -- | -- |Cosmopolite 85. _Dididæ_ | | | | -- |(Extinct) | | | | | GALLINÆ. | | | | | 86. Pteroclidæ | -- | | -- | -- |Palæarctic, Oriental 87. Tetraonidæ | -- | -- | -- | -- |Eastern Hemisphere and | | | | | N. America 88. Phasianidæ | -- | -- | -- | -- |Old World and N. America 89. Turnicidæ | -- | -- | -- | -- |Eastern Hemisphere. | | | | | ACCIPITRES. | | | | | 94. Vulturidæ | -- | -- | -- | |All the continents but | | | | | Australia 95. _Serpentariidæ_ | -- | -- | -- | | 96. Falconidæ | -- | -- | -- | -- |Cosmopolite 97. Pandionidæ | -- | -- | -- | -- |Cosmopolite 98. Strigidæ | -- | -- | -- | -- |Cosmopolite | | | | | GRALLÆ. | | | | | 99. Rallidæ | -- | -- | -- | -- |Cosmopolite 100. Scolopacidæ | -- | -- | -- | -- |Cosmopolite 103. Parridæ | -- | -- | -- | -- |Tropical 104. Glareolidæ | -- | -- | -- | -- |Eastern Hemisphere 105. Charadriidæ | -- | -- | -- | -- |Cosmopolite 106. Otididæ | -- | -- | -- | |Eastern Hemisphere 107. Gruidæ | -- | -- | -- | |All regions but Neotropical 113. Ardeidæ | -- | -- | -- | -- |Cosmopolite 114. Plataleidæ | -- | -- | -- | -- |Almost Cosmopolite 115. Ciconiidæ | -- | -- | -- | -- |Almost Cosmopolite 117. Phoenicopteridæ | -- | -- | -- | -- |Oriental and Neotropical | | | | | ANSERES. | | | | | 118. Anatidæ | -- | -- | -- | -- |Cosmopolite 119. Laridæ | -- | -- | -- | -- |Cosmopolite 120. Procellariidæ | -- | -- | -- | -- |Cosmopolite 121. Pelecanidæ | -- | -- | -- | -- |Cosmopolite 122. Spheniscidæ | | | -- | |South temperate regions 124. Podicipidæ | -- | -- | -- | -- |Cosmopolite 126. Struthionidæ | -- | | -- | |Temperate S. America 131. _Æpyornithidæ_ | | | | -- |(Extinct) | | | | | REPTILIA. | | | | | OPHIDIA. | | | | | 1. Typhlopidæ | -- | -- | -- | -- |All regions but Nearctic 5. Calamariidæ | -- | -- | -- | |Warm parts of all regions 7. Colubridæ | -- | -- | -- | -- |Almost Cosmopolite 8. Homalopsidæ | | -- | | |Oriental, and all other regions 9. Psammophidæ | -- | -- | -- | -- |Oriental and S. Palæarctic 10. _Rachiodontidæ_ | | -- | -- | | 11. Dendrophidæ | -- | -- | -- | -- |Oriental, Australian, | | | | | Neotropical 12. Dryiophidæ | | -- | | -- |Oriental, Neotropical 13. Dipsadidæ | -- | -- | -- | |Oriental, Australian, | | | | | Neotropical 15. Lycodontidæ | -- | -- | -- | |Oriental 17. Pythonidæ | -- | -- | -- | -- |All tropical regions 18. Erycidæ | | -- | | |Oriental, S. Palæarctic 20. Elapidæ | -- | -- | -- | |Tropical regions, S. U. States | | | | | and Japan 21. _Dendraspididæ_ | -- | -- | | | 22. _Atractaspididæ_ | | -- | -- | | 23. Hydrophidæ | | | | -- |Oriental, Australian, Panama 25. Viperidæ | -- | -- | -- | -- |Oriental, Palæarctic | | | | | LACERTILIA. | | | | | 28. Amphisbænidæ | -- | -- | | |S. Europe, Neotropical 29. Lepidosternidæ | | -- | -- | |N. America 30. Varanidæ | -- | -- | -- | |Warm parts of E. Hemisphere 33. Lacertidæ | -- | -- | -- | |All continents but America 34. Zonuridæ | -- | -- | -- | -- |All America, N. India, | | | | | S. Europe 40. _Chamæsauridæ_ | | | -- | | 41. Gymnopthalmidæ | | -- | | -- |Palæarctic, Australian, | | | | | Neotropical 45. Scincidæ | -- | -- | -- | -- |Almost Cosmopolite 47. Sepidæ | -- | -- | -- | -- |South 48. Acontiadæ | | -- | -- | -- |Ceylon and Moluccas 49. Geckotidæ | -- | -- | -- | -- |Almost cosmopolite 51. Agamidæ | -- | -- | -- | -- |Oriental, Australian, | | | | | S. Palæarctic 52. Chamæleonidæ | -- | -- | -- | -- |Oriental, S. Palæarctic | | | | | CROCODILIA. | | | | | 55. Crocodilidæ | -- | -- | -- | -- |Oriental, Neotropical | | | | | CHELONIA. | | | | | 57. Testudinidæ | -- | -- | -- | -- |All continents but Australia 58. Chelydidæ | -- | -- | -- | -- |Australia, S. America 59. Trionychidæ | -- | -- | -- | |Oriental, Japan, E. United | | | | | States 60. Cheloniidæ | | | | |Marine | | | | | AMPHIBIA. | | | | | PSEUDOPHIDIA. | | | | | 1. Cæciliadæ | | -- | | |Oriental, Neotropical | | | | | ANOURA. | | | | | 7. Phryniscidæ | -- | -- | | |Neotropical, Australia, Java 9. Bufonidæ | -- | -- | -- | |All regions but Australian 11. Engystomidæ | | -- | -- | |All regions but Palæarctic 14. Alytidæ | -- | -- | -- | |All regions but Oriental 17. Polypedatidæ | -- | -- | -- | -- |All the regions 18. Ranidæ | -- | -- | -- | -- |Almost Cosmopolite 19. Discoglossidæ | | -- | -- | |All regions but Nearctic 21. _Dactylethridæ_ | -- | -- | -- | | | | | | | FISHES (FRESH-WATER).| | | | | ACANTHOPTERYGII. | | | | | 3. Percidæ | -- | | | |All regions but Australian 12. Scienidæ | -- | -- | -- | |All regions but Australian 35. Labyrinthici | | | -- | -- |Oriental, Moluccas 38. Mugillidæ | -- | -- | -- | -- |Australian, Neotropical 52. Chromidæ | -- | -- | -- | -- |Oriental, Neotropical | | | | | PHYSOSTOMI. | | | | | 59. Siluridæ | -- | -- | -- | -- |All warm regions 60. Characinidæ | -- | -- | | |Neotropical 68. _Mormyridæ_ | -- | -- | | | 69. _Gymnarchidæ_ | -- | -- | | | 73. Cyprinodontidæ | -- | -- | | -- |Palæarctic, Oriental, American 75. Cyprinidæ | -- | -- | -- | -- |Absent from Australia and | | | | | S. America 78. Osteoglossidæ | -- | -- | | |All tropical regions 82. Notopteridæ | | -- | | |Oriental | | | | | GANOIDEI. | | | | | 92. Sirenoidei | -- | -- | | |Neotropical, Australian 94. _Polypteridæ_ | -- | -- | | | | | | | | INSECTS. | | | | | LEPIDOPTERA (PART). | | | | | DIURNI (BUTTERFLIES).| | | | | 1. Danaidæ | -- | -- | -- | -- |All warm countries and Canada 2. Satyridæ | -- | -- | -- | -- |Cosmopolite 3. Elymniidæ | | -- | | |Oriental, Moluccas 6. Acræidæ | -- | -- | -- | -- |All tropical regions 8. Nymphalidæ | -- | -- | -- | -- |Cosmopolite 9. Libytheidæ | | -- | | -- |Absent from Australia only 10. Nemeobiidæ | | -- | | -- |Absent from Australia and | | | | | Nearctic region 13. Lycænidæ | -- | -- | -- | -- |Cosmopolite 14. Pieridæ | -- | -- | -- | -- |Cosmopolite 15. Papilionidæ | -- | -- | -- | -- |Cosmopolite 16. Hesperidæ | -- | -- | -- | -- |Cosmopolite | | | | | SPHINGIDEA. | | | | | 17. Zygænidæ | -- | -- | -- | -- |Cosmopolite 19. Agaristidæ | -- | -- | -- | -- |Australian, Oriental 20. Uraniidæ | | | | -- |All tropical regions 22. Ægeriidæ | -- | -- | -- | -- |Cosmopolite, excl. Australia 23. Sphingidæ | -- | -- | -- | -- |Cosmopolite ---------------------+----+----+----+----+------------------------------- {300}TABLE II. _LIST OF GENERA OF TERRESTRIAL MAMMALIA AND BIRDS INHABITING THE ETHIOPIAN REGION._ EXPLANATION. Names in _italics_ show genera peculiar to the region. Names inclosed thus (......) show genera which just enter the region, but are not considered properly to belong to it. Genera which undoubtedly belong to the region are numbered consecutively. _MAMMALIA._ -------------------+-------+----------------------+---------------------- Order, Family, and | No. of| Range within | Range beyond Genus. |Species| the Region. | the Region. -------------------+-------+----------------------+---------------------- | | | PRIMATES. | | | SIMIIDÆ. | | | | | | 1. _Troglodytes_ | 2 |W. Africa to Western | | | Nile Sources | | | | SEMNOPITHECIDÆ. | | | 2. _Colobus_ | 11 |Abyssinia to West | | | Africa | | | | CYNOPITHECIDÆ. | | | | | | 3. _Myiopithecus_ | 1 |West Africa | 4. _Cercopithecus_| 24 |Tropical Africa | 5. _Cercocebus_ | 5 |West Africa | 6. _Theropithecus_| 2 |North-east Africa, |Palestine | | Arabia | 7. _Cynocephalus_ | 10 |Nubia to Cape, | | | W. Africa, Arabia | | | | (Sub-Order) | | | _LEMUROIDEA._ | | | LEMURIDÆ. | | | | | | 8. _Indris_ | 6 |Madagascar | 9. _Lemur_ | 15 |Madagascar | 10. _Hapalemur_ | 2 |Madagascar | 11. _Microcebus_ | 4 |Madagascar | 12. _Chirogaleus_ | 5 |Madagascar | 13. _Lepilemur_ | 2 |Madagascar | 14. _Perodicticus_ | 1 |Sierra Leone | 15. _Arctocebus_ | 1 |Old Calabar | 16. _Galago_ | 14 |Tropical and S. Africa | | | | CHIROMYIDÆ. | | | | | | 17. _Chiromys_ | 1 |Madagascar | | | | CHIROPTERA. | | | PTEROPIDÆ. | | | | | | 18. Pteropus | 7 |Africa and Madagascar |Tropics of Eastern | | | Hemisphere 19. Xantharpya | 1 |All Africa |Oriental, Austro- | | | Malayan 20. Cynopterus | 1 |Tropical Africa |Oriental 21. _Epomophorus_ | 6 |Tropical Africa and | | | Abyssinia | 22. _Hypsignathus_ | 1 |W. Africa | | | | RHINOLOPHIDÆ. | | | | | | 23. Rhinolophus | 6 |Africa and Madagascar |Warmer parts of | | | Eastern Hemisphere 24. _Macronycterys_| 1 |W. Africa | 25. Phyllorhina | 4 |Tropical Africa |Indo-Malaya, Austro- | | | Malaya 26. Asellia | 1 |Nubia |Indo-Malaya, Austro- | | | Malaya 27. Megaderma | 1 |Senegal, Upper Nile |Oriental, Moluccas 28. Nycteris | 3 |All Africa |Java | | | VESPERTILIONIDÆ. | | | | | | 29. Vespertilio | 14 |Africa and Madagascar |Cosmopolite 30. Kerivoula | 1 |S. Africa |Oriental 31. Miniopteris | 1 |S. Africa |Indo-Malaya 32. Nycticejus | 7 |Tropical Africa |India 33. Taphozous | 2 |Africa and Madagascar |Oriental, Austro- | | | Malayan, Neotropical | | | NOCTILIONIDÆ. | | | | | | 34. Nyctinomus | 1 |Madagascar |Oriental, American, | | | S. Palæarctic 35. Molossus | 3 |Africa, Bourbon |Neotropical, | | | S. Palæarctic | | | INSECTIVORA. | | | MACROSCELIDIDÆ. | | | | | | 36. _Macroscelides_| 2 |South and East Africa |N. Africa 37. _Petrodromus_ | 1 |Mozambique | 38. _Rhynchocyon_ | 1 |Mozambique | | | | ERINACEIDÆ. | | | | | | 39. Erinaceus | 2 |Cen. and South Africa |Palæarctic, N. India | | | CENTETIDÆ. | | | | | | 40. _Centetes_ | 2 |Madagascar and | | | Mauritius | 41. _Hemicentetes_ | 2 |Madagascar | 42. _Ericulus_ | 2 |Madagascar | 43. _Oryzorictes_ | 1 |Madagascar | 44. _Echinops_ | 3 |Madagascar | | | | POTAMOGALIDÆ. | | | | | | 45. _Potamogale_ | 1 |Old Calabar | | | | CHRYSOCHLORIDÆ. | | | | | | 46. _Chrysochloris_| 3 |Cape to Mozambique | | | | SORICIDÆ. | | | | | | 47. Sorex | 15 |All Africa and |Palæarc., Nearc., Ori | | Madagascar | | | | CARNIVORA. | | | FELIDÆ. | | | | | | 48. Felis | 8 |All Africa |All reg. but | | | Australian 49. Lynx[?] | 1 |N. and S. Africa |Palæarctic and | | | Nearctic 50. Cynælurus | 1 |Cape of Good Hope | | | | CRYPTOPROCTIDÆ. | | | | | | 51. _Cryptoprocta_ | 1 |Madagascar | | | | VIVERRIDÆ. | | | | | | 52. Viverra | 1 |Tropical Africa |Oriental 53. Genetta | 4 |Tropical and S. Africa |S. Palæarctic 54. _Fossa_ | 2 |Madagascar | 55. _Poiana_ | 1 |W. Africa | 56. _Galidia_ | 3 |Madagascar | 57. _Nandinia_ | 1 |W. Africa | 58. _Galidictis_ | 2 |Madagascar | 59. Herpestes | 13 |All Africa |S. Europe, Oriental 60. _Athylax_ | 3 |S. and E. Africa(?) | | | Madagascar | 61. Calogale | 9 |Tropical and S. Africa |Oriental 62. _Galerella_ | 1 |E. Africa | 63. _Ariela_ | 1 |S. Africa | 64. _Ichneumia_ | 4 |E. Africa, Senegal, | | | S. Africa | 65. _Bdeogale_ | 3 |Tropical Africa | 66. _Helogale_ | 2 |E. and S. Africa | 67. _Cynictis_ | 3 |S. Africa | 68. _Rhinogale_ | 1 |E. Africa | 69. _Mungos_ | 3 |Tropical and S. Africa | 70. _Crossarchus_ | 1 |Tropical Africa | 71. _Eupleres_ | 1 |Madagascar | 72. _Suricata_ | 1 |S. Africa | | | | PROTELIDÆ. | | | | | | 73. _Proteles_ | 1 |S. Africa | | | | HYÆNIDÆ. | | | | | | 74. Hyæna | 3 |All Africa |S. Palæarctic, India | | | CANIDÆ. | | | | | | 75. _Lycaon_ | 1 |S., Central, and | | | E. Africa | 76. Canis | 5 |All Africa |Almost Cosmopolitan 77. _Megalotis_ | 1 |S. Africa | | | | MUSTELIDÆ. | | | | | | 78. Mustela | 1 |Angola |Palæarctic, Nearctic 79. Gymnopus[?] | 1 |S. Africa |Oriental 80. Aonyx | 1 |S. and W. Africa |Oriental 81. _Hydrogale_ | 1 |S. Africa | 82. Mellivora | 2 |South and Tropical |India | | Africa | 83. _Ictonyx_ | 2 |Tropical and S. Africa | | | | OTARIIDÆ. | | | | | | 84. Arctocephalus | 1 |Cape of Good Hope |South Temperate Zone | | | SIRENIA. | | | MANATIDÆ. | | | | | | 85. Manatus | 1 |W. Africa |Tropical America 86. Halicore | 1 |E. Africa |Oriental and | | | Australian | | | UNGULATA. | | | EQUIDÆ. | | | | | | 87. Equus | 3 |Tropical and S. Africa |Palæarctic | | | RHINOCEROTIDÆ. | | | | | | 88. Rhinoceros | 4 |All Tropical and |Oriental | | S. Africa | | | | HIPPOPOTAMIDÆ. | | | | | | 89. _Hippopotamus_ | 2 |Great Rivers of Africa | | | | SUIDÆ. | | | | | | 90. _Potamochoerus_| 3 |Tropical Africa and | | | Madg. | 91. _Phacochoerus_ | 2 |Abyssinia to Caffraria | | | | TRAGULIDÆ. | | | | | | 92. _Hyomoschus_ | 1 |W. Africa | | | | CAMELOPARDALIDÆ. | | | | | | 93._Camelopardalis_| 1 |All open country | | | | BOVIDÆ. | | | | | | 94. Bubalus | 3 |Trop. and S. Africa |India 95. _Oreas_ | 2 |Africa S. of Sahara | 96. _Tragelaphus_ | 8 |Africa S. of Sahara | 97. Oryx | 3 |Arabian and African |S. Palæarctic | | deserts | 98. Gazella | 12 |Africa N. of Equator |Palæarctic Deserts | | and S. Africa | 99. _Æpyceros_ | 1 |S. E. Africa | 100. _Cervicapra_ | 4 |All Tropical Africa | 101. _Kobus_ | 6 |Pastures of all Africa | 102. _Pelea_ | 1 |South Africa | 103. _Nanotragus_ | 9 |Africa S. of Sahara | 104. _Neotragus_ | 1 |Abyssinia and | | | N. E. Africa | 105. _Cephalophus_ | 22 |All tropical Africa | 106. _Hippotragus_ | 3 |Gambia, Central Africa | | | to Cape | 107. _Alcephalus_ | 9 |All Africa | 108. _Catoblepas_ | 2 |Africa S. of Equator | (Capra | 1 |Abyssinia, high) |Palæarctic genus | | | PROBOSCIDEA. | | | | | | ELEPHANTIDÆ. | | | | | | 109. Elephas | 1 |Tropical and S. Africa |Oriental | | | HYRACOIDEA. | | | HYRACIDÆ. | | | | | | 110. Hyrax | 10 |Tropical and S. Africa |Syria | | | RODENTIA. | | | MURIDÆ. | | | | | | 111. Mus | 26 |All Africa |E. Hemis. excl. | | | Oceania 112. _Lasiomys_ | 1 |W. Africa | 113. Acanthomys | 4 |Tropical Africa |India 114. _Cricetomys_ | 1 |Tropical Africa | 115. _Saccostomus_ | 2 |Mozambique | 116. _Dendromys_ | 2 |S. Africa | 117. _Nesomys_ | 1 |Madagascar | 118. _Steatomys_ | 2 |East and S. Africa | 119. _Pelomys_ | 1 |Mozambique | 120. _Otomys_ | 6 |S. and E. Africa | 121. Meriones | 14 |Africa |Palæarctic, India 122. _Malacothrix_ | 2 |S. Africa | 123. _Mystromys_ | 1 |S. Africa | 124._Brachytarsomys_| 1 |Madagascar | 125. _Hypogeomys_ | 1 |Madagascar | 126. _Lophiomys_ | 1 |S. Arabia and | | | N. E. Africa | | | | SPALACIDÆ. | | | | | | 127. Rhizomys | 4 |Abyssinia |Oriental to Malacca 128. _Bathyerges_ | 1 |S. Africa | 129. _Georychus_ | 6 |E. Central, and | | | S. Africa | 130. _Heliophobius_ | 1 |Mozambique | | | | DIPODIDÆ. | | | | | | 131. Dipus | 7 |N. and Central Africa |Central Palæarctic 132. _Pedetes_ | 1 |S. Af. to Mozambique | | | and Angola | | | | MYOXIDÆ. | | | | | | 133. Myoxus | 1 |Africa to Cape |Palæarctic | | | SCIURIDÆ. | | | | | | 134. Sciurus | 18 |All woody districts of |All regions but | | Africa | Australia 135. _Anomalurus_ | 5 |W. Africa and Fernando | | | Po. | | | | OCTODONTIDÆ. | | | | | | 136. _Pectinator_ | 1 |Abyssinia | | | | ECHIMYIDÆ. | | | | | | 137. _Petromys_ | 1 |S. Africa | 138. _Aulacodes_ | 1 |W., E., and S. Africa | | | | HYSTRICIDÆ. | | | | | | 139. Hystrix | 1 |Africa to Cape |S. Palæarctic Oriental 140. Atherura | 1 |W. Africa |Palæarctic | | | LEPORIDÆ. | | | | | | 141. Lepus | 5 |East and South Africa |All regions but | | | Australian | | | EDENTATA. | | | MANIDIDÆ. | | | | | | 142. Manis | 4 |Sennaar to W. Africa |Oriental | | and Cape | | | | ORYCTEROPODIDÆ. | | | | | | 143. _Orycteropus_ | 2 |N. E. Africa to Nile | | | Sources, and S. Africa| _BIRDS._ PASSERES. | | | TURDIDÆ. | | | | | | 1. Turdus | 13 |The whole reg. (excl. |Almost Cosmopolite | | Madagas.) | 2. Monticola | 2 |S. Africa |Palæarctic and | | | Oriental 3. _Chætops_ | 3 |S. Africa | 4. _Bessonornis_ | 15 |The whole region |Palestine | | | SYLVIIDÆ. | | | | | | 5. { _Drymoeca_ | 70 |The whole region |Palestine 6. { Cisticola | 13 |The whole region |Palæarc., Orien., { | | | Austral. 7. { Sphenoeacus | 1 |S. Africa |Australian 8. { _Camaroptera_| 5 |Africa | | | | 9. { Acrocephalus | 8 |The whole region |Palæarc., Orien., { | | | Austral. 10. { Bradyptetus | 8 |Abyssinia and S. Africa|S. Europe, Palestine 11. { _Catriscus_ | 3 |All Africa | 12. { _Bernieria_ | 1 |Madagascar | 13. { _Ellisia_ | 1 |Madagascar | 14. { _Mystacornis_| 1 |Madagascar | | | | 15. { Phylloscopus | 1 |S. Africa |Palæarctic, Oriental 16. { _Eremomela_ | 16 |All Africa | 17. { _Eroessa_ | 1 |Madagascar | 18. { Hypolais | 2 |S. Africa |Palæarctic, Oriental | | | 19. { Aedon | 8 |E. and S. Africa |Palæarctic 20. { Sylvia | 3 |N. E. Africa, Gambia, |Palæarctic, Oriental { | | Cape Verd Ids. | 21. { Curruca | 2 |S. Africa |Palæarctic | | | 22. { Ruticilla | 2 |Abyssinia and Senegal |Palæarctic, Oriental 23. { Cyanecula | 2 |N. E. Africa |Palæarctic | | | 24. { Copsychus | 2 |Madagascar and |Oriental { | | Seychelle Ids. | 25. { Thamnobia | 7 |All Africa |Oriental 26. {_Cercotrichas_| 2 |W. and N. E. Africa | 27. { _Poeoptera_ | 1 |W. Africa | 28. { _Gervasia_ | 2 |Madagascar and | { | | Seychelle Ids. | 29. { Dromolæa | 13 |All Africa |S. Palæarctic, India 30. { Saxicola | 14 |Central, E. and |Palæarctic, India { | | S. Africa | 31. { Cercomela | 3 |N. E. Africa |Palestine, N. W. India 32. { Pratincola | 7 |Africa and Madagascar |Palæarctic, Oriental | | | TIMALIIDÆ. | | | | | | 33. Chatarrhæa | 1 |Abyssinia |Oriental, Palestine 34. _Crateropus_ | 17 |All Africa |N. Africa, Persia 35. _Hypergerus_ | 1 |W. Africa | 36. _Cichladusa_ | 3 |W. and E. Africa | 37. _Alethe_ | 4 |W. Africa | 38. _Oxylabes_ | 2 |Madagascar | | | | CINCLIDÆ.[?] | | | | | | 39. _Mesites_ | 1 |Madagascar | | | | TROGLODYTIDÆ.[?] | | | | | | 40. Sylvietta | 2 |Central, E. and | | | S. Africa | | | | SITTIDÆ. | | | | | | 41. _Hypherpes_ | 1 |Madagascar | | | | PARIDÆ. | | | | | | 42. Parus | 5 |All Africa |Palæarc., Orien., | | | Nearc. 43. _Parisoma_ | 5 |All Africa | 44. Ægithalus | 4 |W., Central, and |Palæarctic | | S. Africa | 45. _Parinia_ | 1 |W. Africa, Prince's | | | Island | | | | PYCNONOTIDÆ. | | | | | | 46. Pycnonotus | 8 |All Africa |S. Palæarctic, | | | Oriental 47._Phyllastrephus_| 4 |W. and S. Africa | 48. Hypsipetes | 4 |Madagascar and |Oriental | | Mascarene Ids. | 49. _Tylas_ | 1 |Madagascar | 50. Criniger | 14 |W. and S. Africa |Oriental 51. _Ixonotus_ | 8 |W. Africa | 52. _Andropadus_ | 9 |Africa and Madagascar | 53. _Lioptilus_ | 1 |S. Africa | | | | ORIOLIDÆ. | | | | | | 54. Oriolus | 10 |All Africa |Palæarctic, Oriental 55. _Artamia_[?] | 3 |Madagascar | 56._Cyanolanius_[?]| 1 |Madagascar | | | | CAMPEPHAGIDÆ. | | | | | | 57. _Lanicterus_ | 5 |All Africa | 58. _Oxynotus_ | 2 |Mauritius and Bourbon | 59. Campephaga | 5 |The whole region |Celebes to New | | | Caledonia | | | DICRURIDÆ. | | | | | | 60. Dicrurus | 11 |The whole region |Oriental, Australian | | | MUSCICAPIDÆ. | | | | | | 61. Butalis | 3 |All Africa |Palæarctic, | | | N. Oriental 62. Muscicapa | 10 |All tropical Africa |Palæarctic 63. Alseonax | 4 |S. Africa |Oriental 64. _Newtonia_ | 1 |Madagascar | 65. _Hyliota_ | 2 |W. Africa | 66. _Erythrocercus_| 2 |Tropical Africa | 67. _Artomyias_ | 2 |W. Africa | 68. _Pseudobias_ | 1 |Madagascar | 69. _Smithorius_ | 2 |W. and S. Africa | 70. _Megabias_ | 1 |W. Africa | 71. _Cassinia_ | 2 |W. Africa | 72. _Bias_ | 1 |Tropical Africa | 73. _Elminia_ | 2 |Tropical Africa | 74. _Platystira_ | 12 |All Africa | 75. Tchitrea | 18 |The whole region |Oriental 76. _Pogonocichla_ | 1 |S. Africa | 77. _Bradyornis_ | 7 |All Africa | | | | LANIIDÆ. | | | | | | 78. _Parmoptila_[?]| 1 |W. Africa. | 79. _Calicalicus_ | 1 |Madagascar | 80. Lanius | 15 |All Africa |Palæarc., Orien., | | | Nearc. 81. _Hypocolius_ | 1 |Abyssinia | 82. _Corvinella_ | 1 |S. and W. Africa | 83. _Urolestes_ | 1 |S. Africa | 84. _Fraseria_ | 2 |W. Africa | 85. _Hypodes_ | 1 |W. Africa | 86. _Cuphoterus _ | 1 |Prince's Island | 87. _Nilaus_ | 1 |All Africa | 88. _Prionops_ | 9 |All Africa | 89. _Eurocephalus_ | 2 |N. E. and S. Africa | 90. _Chaunonotus_ | 1 |W. Africa | 91. _Vanga_ | 4 |Madagascar | 92. _Laniarius_ | 38 |All Africa, | | | Madagascar[?] | 93. _Meristes_ | 2 |W. and S. E. Africa | 94. _Nicator_ | 1 |E. Africa | 95. _Telephonus_ | 10 |All Africa |N. Africa | | | CORVIDÆ. | | | | | | 96. _Ptilostomus_ | 2 |W. and E. Africa | 97. Corvus | 7 |All Africa and |Cosmop., excl. | | Madagascar | S. Amer. 98. _Corvultur_ | 2 |N. E. to S. Africa | 99. _Picathartes_ | |W. Africa | (Fregilus | 1 |Abyssinia) |Palæarctic genus | | | NECTARINIIDÆ. | | | | | | 100. _Nectarinia_ | 55 |The whole region | 101. _Promerops_ | 1 |S. Africa | 102._Cinnyricinclus_| 4 |W. Africa | 103. _Neodrepanis_ | 1 |Madagascar | | | | DICÆIDÆ. | | | | | | 104. Zosterops | 23 |The whole region |Oriental and | | | Australian 105. _Pholidornis_ | 1 |W. Africa | | | | HIRUNDINIDÆ. | | | | | | 106. Hirundo | 17 |The whole region |Cosmopolite 107. _Psalidoprogne_| 10 |The whole region | 108. _Phedina_ | 2 |Madagascar and | | | Mauritius | 109. Petrochelidon | 1 |S. Africa |Neotropical 110. Chelidon | 1 |Bogos-land |Palæarctic, Oriental 111. Cotyle | 6 |All Africa |Palæarctic, Oriental 112. _Waldenia_ | 1 |W. Africa | | | | FRINGILLIDÆ. | | | | | | 113. Dryospiza | 8 |All Africa |S. Palæarctic 114. Chlorospiza | 4 |Abyssinia to Cape |Palæarctic 115. Passer | 18 |All Africa |Palæarctic, Oriental 116. _Crithagra_ | 12 |All Africa |N. Africa, Syria 117. _Ligurnus_ | 2 |W. Africa | (Erythrospiza | 1 |Nubia, Arabia) |S. Palæarctic genus 118. Pinicola[?] | 1 |Cameroons, W. Africa |N. Temperate genus 119. _Fringillaria_ | 9 |All Africa |South Palæarctic | | | PLOCEIDÆ. | | | | | | 120. _Textor_ | 5 |All Africa | 121. _Hyphantornis_ | 32 |Tropical and S. Africa | 122. _Symplectes_ | 8 |Tropical and S. Africa | 123. _Malimbus_ | 9 |W. and E. Africa | 124. Ploceus | 2 |W. and E. Africa |Oriental 125. _Nelicurvius_ | 1 |Madagascar | 126. _Foudia_ | 11 |Tropical Africa, | | | Madagascar, &c. | 127. _Sporopipes_ | 1 |Tropical and S. Africa | 128. _Pyromelana_ | 12 |Tropical and S. Africa | 129. _Philetærus_ | 1 |S. Africa | 130. _Nigrita_ | 7 |W. and N. E. Africa | 131. _Plocepasser_ | 4 |E. and S. Africa | 132. _Vidua_ | 6 |Tropical and S. Africa | 133. _Colliuspasser_| 9 |Tropical and S. Africa | 134. _Chera_ | 1 |S. Africa | 135. _Spermospiza_ | 2 |W. Africa | 136. _Pyrenestes_ | 6 |Tropical and S. Africa | 137. Estrilda | 16 |Tropical and S. Africa |Oriental 138. _Pytelia_ | 20 |Tropical and S. Africa | 139. _Hypargos_ | 2 |E. Africa, Madagascar | 140. _Amadina_ | 6 |Tropical and S. Africa | 141. _Spermestes_ | 7 |The whole region | 142. _Amauresthes_ | 1 |E. and W. Africa | 143. _Hypochera_ | 2 |Tropical and S. Africa | | | | STURNIDÆ. | | | | | | 144. _Dilophus_ | 1 |S. Africa, Loanda, | | | Sennaar | 145. _Buphaga_ | 2 |Trop. and S. Africa | | | ([?] a family) | 146. _Euryceros_ | 1 |Madagascar ([?] a | | | family) | 147. _Juida_ | 5 |Tropical and S. Africa | 148. _Lamprocolius_ | 16 |Tropical and S. Africa | 149._Cinnyricinclus_| 2 |Tropical and S. Africa | 150. _Onychognathus_| 2 |W. Africa | 151. _Spreo_ | 5 |Tropical and S. Africa | 152. _Amydrus_ | 5 |N. E. Africa |Palestine 153. _Hartlaubius_ | 1 |Madagascar | 154. _Falculia_ | 1 |Madagascar | 155. _Fregilupus_ | 1 |Bourbon | | | | ALAUDIDÆ. | | | | | | 156. Alauda | 3 |Abyssinia and |Palæarctic, Indian | | S. W. Africa | 157. _Spizocorys_ | 1 |South Africa | 158. Galerida | 4 |North of tropical |Palæarctic, Indian | | Africa | 159. _Calendula_ | 2 |Abyssinia, S. Africa | (Melanocorypha | 1 |Abyssinia) |Palæarctic genus 160. Certhilauda | 3 |South Africa |S. Europe 161. Alaemon | 3 |South Africa |S. Palæarctic 162. _Heterocorys_ | 1 |South Africa | 163. Mirafra | 10 |South Africa, |Oriental, Australian | | Madagascar | 164. Ammomanes | 4 |African deserts |S. Palæarctic, Indian 165. _Megalophonus_ | 5 |Tropical and S. Africa | 166. _Tephrocorys_ | 2 |S. Africa | 167. Pyrrhulauda | 6 |Tropical and S. Africa |Oriental, Canary | | | Islands | | | MOTACILLIDÆ. | | | | | | 168. Budytes | 8 |The whole region |Palæarctic, Oriental, | | |Australian | | | 169. Anthus | 10 |Tropical and S. Africa |All regions, exc. | | | Australia 170. _Macronyx_ | 4 |Tropical and S. Africa | | | | PITTIDÆ. | | | | | | 171. Pitta | 1 |W. Africa |Oriental, Australian | | | PAICTIDÆ. | | | | | | 172. _Philepitta_ | 2 |Madagascar | | | | PICARIÆ. | | | | | | PICIDÆ. | | | | | | 173. _Verreauxia_ | 1 |W. Africa | 174. _Dendropicus_ | 14 |Tropical and S. Africa | 175. _Campethera_ | 14 |Tropical and S. Africa | 176. _Geocolaptes_ | 1 |South Africa | | | | YUNGIDÆ. | | | | | | 177. Yunx | 1 |N. E. Africa, S. Africa|Palæarctic | | | INDICATORIDÆ. | | | | | | 178. Indicator | 8 |Tropical and S. Africa |Oriental | | | MEGALÆMIDÆ. | | | | | | 179._Pogonorhynchus_| 14 |Tropical and S. Africa | 180. _Buccanodon_ | 1 |West Africa | 181. _Stactolæma_ | 1 |West Africa | 182. _Barbatula_ | 9 |West and South Africa | 183. _Xylobucco_ | 3 |West and South Africa | 184. _Gymnobucco_ | 3 |West Africa | 185. _Trachyphonus_ | 6 |Tropical and South | | | Africa | | | | MUSOPHAGIDÆ. | | | | | | 186. _Musophaga_ | 2 |West Africa | 187. _Turacus_ | 10 |Tropical and S. Africa | 188. _Schizorhis_ | 6 |Tropical and S. Africa | | | | COLIIDÆ. | | | | | | 189. _Colius_ | 7 |Tropical and S. Africa | | | | CUCULIDÆ. | | | | | | 190. _Ceuthmochares_| 2 |Africa and Madagascar | 191. _Coua_ | 9 |Madagascar | 192._Cochlothraustes_ 1 |Madagascar | 193. _Centropus_ | 8 |Africa and Madagascar |Oriental, Australian 194. Cuculus | 10 |Africa and Madagascar |Palæarc., Orien., | | | Austral. 195. Chrysococcyx | 7 |Tropical and S. Africa |Oriental, Australian 196. Coccystes | 6 |Tropical and S. Africa |S. Palæarctic, | | | Oriental | | | LEPTOSOMIDÆ. | | | | | | 197. _Leptosomus_ | 1 |Madagascar | | | | CORACIIDÆ. | | | | | | 198. Coracias | 5 |Africa and Madagascar |S. Palæarctic, | | | Oriental 199. Eurystomus | 3 |Africa and Madagascar |Oriental, Australian 200. _Atelornis_ | 2 |Madagascar | 201._Brachypteracias_ 1 |Madagascar | 202. _Geobiastes_ | 1 |Madagascar | | | | MEROPIDÆ. | | | | | | 203. Merops | 11 |Africa and Madagascar |S. Palæar., Orien., | | | Austral. 204. _Melittophagus_| 5 |Tropical and S. Africa | | | | TROGONIDÆ. | | | | | | 205. _Apaloderma_ | 2 |Tropical and S. Africa | | | | ALCEDINIDÆ. | | | | | | 206. Alcedo | 2 |W. Africa, Abyssinia, |Palæar., Orien., | | Natal | Austral. 207. _Corythornis_ | 3 |Africa and Madagascar | 208. Ceryle | 1 |W. Africa, Abyssinia, |American, Palæarctic | | Natal | 209. _Myioceyx_ | 2 |West Africa | 210. _Ispidina_ | 4 |Africa and Madagascar | 211. Halcyon | 10 |Africa, Prince's Is., |S. Palæar., Orien., | | St. Thomé | Austral. | | | BUCEROTIDÆ. | | | | | | 212. Berenicornis | 1 |West Africa |Malaya 213. _Tockus_ | 12 |Tropical and S. Africa | 214. _Bycanistes_ | 6 |Tropical and S. Africa | 215. _Bucoreus_ | 2 |Tropical and S. Africa | | | | UPUPIDÆ. | | | | | | 216. Upupa | 3 |Africa and Madagascar |S. Palæarctic, | | | Oriental | | | IRRISORIDÆ. | | | | | | 217. _Irrisor_ | 12 |Africa and Madagascar | | | | CAPRIMULGIDÆ. | | | | | | 218. Caprimulgus | 18 |Africa and Madagascar |Palæarc., Orien., | | | Austral. 219. _Scortornis_ | 3 |Tropical Africa | 220. _Macrodipteryx_| 2 |W. Africa to Abyssinia | 221. _Cosmetornis_ | 1 |Tropical Africa to the | | | Zambesi | | | | CYPSELIDÆ. | | | | | | 222. Cypselus | 6 |The whole region |Palæarctic, Oriental 223. Collocalia | 1 |Mascarene Ids., |Oriental, Australian | | Madagascar | 224. Chætura | 4 |Tropical Africa and |Cosmop., exc. | | Madagascar | W. Palæarctic | | | PSITTACI. | | | PALÆORNITHIDÆ. | | | | | | 225. Palæornis | 3 |W. Africa to Abys. & |Oriental | | Mauritius | | | | PSITTACIDÆ. | | | | | | 226. _Coracopsis_ | 5 |Madagascar and | | | Seychelle Ids. | 227. _Psittacus_ | 2 |W. Africa | 228. _Poeocephalus_ | 9 |Tropical and S. Africa | 229. _Agapornis_ | 4 |Tropical and S. Africa | 230. _Poliopsitta_ | 2 |Trop. Africa and | | | Madagascar | | | | COLUMBÆ. | | | COLUMBIDÆ. | | | | | | 231. Treron | 6 |Africa and Madagascar |Oriental 232. _Alectrænas_ | 5 |Madagascar and Masc. | | | Ids. (extct. in | | | Mauritius and | | | Rodriguez) | 233. Columba | 12 |Africa and Madagascar |Palæarctic, Oriental 234. _Oena_ | 1 |Tropical and S. Africa | 235. Turtur | 10 |Africa, Madagascar, |Palæarctic, Oriental | | Comoro and Seychelle | | | Islands | 236. _Aplopelia_ | 4 |Abyssinia, S. Africa | | | and West African | | | Islands | 237. _Chalcopelia_ | 3 |Tropical and S. Africa | | | | DIDIDÆ. (extinct) | | | | | | 238. _Didus_ | 5 |Mascarene Islands | | | | GALLINÆ. | | | PTEROCLIDÆ. | | | | | | 239. Pterocles | 9 |Africa and Madagascar |S. Palæarctic, Indian | | | TETRAONIDÆ. | | | | | | 240. _Ptilopachus_ | 1 |West Africa | 241. Francolinus | 30 |Africa and Madagascar |S. Palæarctic, Indian 242. _Peliperdix_ | 1 |West Africa | 243. _Margaroperdix_| 1 |Madagascar | 244. Coturnix | 2 |Tropical and S. Africa |Palæar., Orient., | | | Austral. (Caccabis | 1 |Abyssinia) |Palæarctic genus | | | PHASIANIDÆ. | | | | | | 245. _Phasidus_ | 1 |West Africa | 246. _Agelastes_ | 1 |West Africa | 247. _Acryllium_ | 1 |West Africa | 248. _Numida_ | 9 |Africa to Natal and | | | Madagascar | | | | TURNICIDÆ. | | | | | | 249. Turnix | 4 |S. Africa and |Palæarc., Orient., | | Madagascar | Austrl. 250. _Ortyxelos_ | 1 |Africa | | | | ACCIPITRES. | | | VULTURIDÆ. | | | | | | 251. Gyps | 2 |Africa, except W. |Palæarctic, Oriental | | sub-region | 252. Pseudogyps | 1 |N. E. Africa to Senegal|Oriental 253. Otogyps | 1 |N. E. and S. Africa |Palæarctic, Oriental 254. _Lophogyps_ | 1 |N. E. and S. Africa and| | | Senegal | 255. Neophron | 2 |Africa, excl. west |S. Palæarctic, | | coast | Oriental | | | FALCONIDÆ. | | | | | | 256. _Polyboroides_ | 2 |Africa and Madagascar | 257. Circus | 4 |Africa and Madagascar |Almost Cosmopolite 258. _Urotriorchis_ | 1 |W. Africa | 259. _Melierax_ | 5 |Africa, excl. west | | | coast | 260. Astur | 5 |Africa and Madagascar |Almost Cosmopolite 261. _Nisoides_ | 1 |Madagascar | 262. _Eutriorchis_ | 1 |Madagascar | 263. Accipiter | 8 |Africa and Madagascar |Almost Cosmopolite 264. Buteo | 5 |Africa and Madagascar |Cosmop., excl. | | | Austral. 265. Gypaëtus | 1 |N. E. and S. Africa |S. Palæarctic 266. Aquila | 5 |All Africa |Nearc., Palæarc., | | | Indian 267. Nisaëtus | 1 |W. Africa |S. Palæarctic, | | | Oriental, Australia 268. Spizaëtus | 3 |All Africa |Neotropical, Oriental | | | to N. Guinea 269. _Lophoætus_ | 1 |All Africa | 270. _Asturinula_ | 1 |Tropical Africa | 271. _Dryotriorchis_| 1 |W. Africa | 272. Circaëtus | 5 |All Africa |Palæarctic, Oriental 273. Butastur | 1 |N. E. Africa |Oriental to New Guinea 274. _Helotarsus_ | 2 |Tropical and S. Africa | 275. Haliæetus | 2 |The whole region |Cosmopolite, excl. | | | Neotropical region 276. _Gypohierax_ | 1 |West and East Africa | 277. _Elanoides_ | 1 |West and N. E. Africa | 278. Milvus | 1 |The whole region |The Eastern Hemisphere 279. Elanus | 1 |Africa |India to Australia 280. Machærhamphus | 1 |S. W. Africa and |Malacca | | Madagascar | 281. Pernis | 1 |S. Africa and |Palæarctic, Oriental | | Madagascar | 282. Baza | 3 |Africa and Madagascar |India to N. Australia 283. Poliohierax | 1 |East Africa |Burmah 284. Falco | 4 |All Africa |Almost Cosmopolite 285. Cerchneis | 8 |The whole region |Almost Cosmopolite | | | SERPENTARIIDÆ. | | | | | | 286. _Serpentarius_ | 1 |The greater part of | | | Africa | | | | PANDIONIDÆ. | | | | | | 287. Pandion | 1 |All Africa |Cosmopolite | | | STRIGIDÆ. | | | | | | 288. Athene | 5 |Africa and Madagascar, |Palæarctic, Oriental, | | Rodriquez (extinct) | Australian 289. Bubo | 8 |Africa and Madagascar |Cosmopolite 290. _Scotopelia_ | 2 |West and S. Africa to | | | Zambesi | 291. Scops | 3 |W. and S. Africa, |Almost Cosmopolite | | Madagascar, Comoro | | | Islands | 292. Syrnium | 2 |Africa |Palæarctic, Oriental, | | | American 293. Asio | 1 |N. E. and S. Africa |Cosmopolite 294. Strix | 4 |Africa and Madagascar |Cosmopolite _Peculiar or very Characteristic Genera of Wading or Swimming Birds._ GRALLÆ. | | | RALLIDÆ. | | | | | | _Himantornis_ | 1 |West Africa | Podica | 3 |Africa |Burmah | | | GLAREOLIDÆ. | | | | | | Cursorius | 8 |All Africa |S. Europe, India | | | OTIDIDÆ. | | | | | | Eupodotis | 16 |All Africa |India, Australia | | | GRUIDÆ. | | | | | | _Balearica_ | 2 |All Africa | | | | ARDEIDÆ. | | | | | | _Balæniceps_ | 1 |Upper Nile | | | | PLATALEIDÆ. | | | | | | _Scopus_ | 1 |Tropical and S. Africa | | | | ANSERES. | | | ANATIDÆ. | | | | | | _Thalassornis_| 1 |South Africa | | | | STRUTHIONES. | | | STRUTHIONIDÆ. | | | | | | 295. _Struthio_ | 2 |All Africa |Syria | | | ÆPYORNITHIDÆ. | |(Extinct) | | | | 296. _Æpyornis_ | 3[?]|Madagascar | {314}CHAPTER XII. THE ORIENTAL REGION. This region is of comparatively small extent, but it has a very diversified surface, and is proportionately very rich. The deserts on the north-west of India are the debatable land that separates it from the Palæarctic and Ethiopian regions. The great triangular plateau which forms the peninsula of India is the poorest portion of the region, owing in part to its arid climate and in part to its isolated position; for there can be little doubt that in the later Tertiary period it was an island, separated by an arm of the sea (now forming the valleys of the Ganges and Indus) from the luxuriant Himalayan and Burmese countries. Its southern extremity, with Ceylon, has a moister climate and more luxuriant vegetation, and exhibits indications of a former extension southwards, with a richer and more peculiar fauna, partly Malayan and partly Mascarene in its character. The whole southern slopes of the Himalayas, with Burmah, Siam and Western China, as well as the Malay peninsula and the Indo-Malay islands, are almost everywhere covered with tropical forests of the most luxuriant character, which abound in varied and peculiar forms of vegetable and animal life. The flora and fauna of this extensive district are essentially of one type throughout; yet it may be usefully divided into the Indo-Chinese and the Malayan sub-regions, as each possesses a number of peculiar or characteristic animals. The former sub-region, besides having many tropical and sub-tropical types of its own, also possesses a large number of peculiarly modified temperate forms on the mountain ranges of its northern boundary, which are wholly wanting in the Malayan sub-region. The Philippine islands are best classed with the Indo-Malay group, although they are strikingly deficient in many Malayan types, and exhibit an approach to the Celebesian division of the Austro-Malay sub-region. [Illustration: ORIENTAL REGION] {315}_Zoological Characteristics of the Oriental Region._--The Oriental Region possesses examples of 35 families of Mammalia, 71 of Birds, 35 of Reptiles, 9 of Amphibia, and 13 of Fresh-water Fishes. Of these 163 families, 12 are peculiar to the region; namely, Tarsiidæ, Galeopithecidæ, and Tupaiidæ among Mammalia, while Æluridæ, though confined to the higher Himalayas, may perhaps with more justice be claimed by the Palæarctic region; Liotrichidæ, Phyllornithidæ, and Eurylæmidæ among birds; Xenopeltidæ (extending, however, to Celebes), Uropeltidæ, and Acrochordidæ among reptiles; Luciocephalidæ, Ophiocephalidæ and Mastacembelidæ among fresh-water fishes. A number of other families are abundant, and characteristic of the region; and it possesses many peculiar and characteristic genera, which must be referred to somewhat more in detail. _Mammalia._--The Oriental region is rich in quadrumana, and is especially remarkable for its orang-utans and long-armed apes (_Simia_, _Hylobates_, and _Siamanga_); its abundance of monkeys of the genera _Presbytes_ and _Macacus_; its extraordinary long-nosed monkey (_Presbytes nasalis_); its Lemuridæ (_Nycticebus_ and _Loris_); and its curious genus _Tarsius_, forming a distinct family of lemurs. All these quadrumanous genera are confined to it, except _Tarsius_ which extends as far as Celebes. It possesses more than 30 genera of bats, which are enumerated in the lists given at the end of this chapter. In Insectivora it is very rich, and possesses several remarkable forms, such as the flying lemur (_Galeopithecus_); the squirrel-like Tupaiidæ consisting of three genera; and the curious _Gymnura_ allied to the hedgehogs. In Carnivora, it is especially rich in many forms of civets (Viverridæ), possessing 10 peculiar genera, among which _Prionodon_ and _Cynogale_ are remarkable; numerous Mustelidæ, of which _Gymnopus_, _Mydaus_, _Aonyx_ and _Helictis_ are the most conspicuous; _Ælurus_, a curious animal, cat-like in appearance but {316}more allied to the bears, forming a distinct family of Carnivora, and confined to the high forest-districts of the Eastern Himalayas and East Thibet; _Melursus_ and _Helarctos_, peculiar forms of bears; _Platanista_, a dolphin peculiar to the Ganges and Indus. Among Ruminants it has the beautiful chevrotain, forming the genus _Tragulus_ in the family Tragulidæ; with one peculiar genus and three peculiar sub-genera of true deer. The Antilopinæ and Caprinæ are few, confined to limited districts and not characteristic of the region; but there are everywhere wild cattle of the genera _Bibos_ and _Bubalus_, which, with species of _Rhinoceros_ and _Elephas_, form a prominent feature in the fauna. The Rodents are less developed than in the Ethiopian region, but several forms of squirrels everywhere abound, together with some species of porcupine; and the Edentata are represented by the scaly manis. _Birds._--The families and genera of birds which give a character to Oriental lands, are so numerous and varied, that we can here only notice the more prominent and more remarkable. The Timaliidæ, represented by the babblers (_Garrulax_, _Pomatorhinus_, _Timalia_, &c.), are almost everywhere to be met with, and no less than 21 genera are peculiar to the region; the elegant fork-tailed _Enicurus_ and rich blue _Myiophonus_, though comparatively scarce, are characteristic of the Malayan and Indo-Chinese faunas; the elegant little "hill-tits" (Liotrichidæ) abound in the same part of the region; the green bulbuls (_Phyllornis_) are found everywhere; as are various forms of Pycnonotidæ, the black and crimson "minivets" (_Pericrocotus_), and the glossy "king-crows" (_Dicrurus_); _Urocissa_, _Platylophus_ and _Dendrocitta_ are some of the interesting and characteristic forms of the crow family; sun-birds (Nectariniidæ) of at least three genera are found throughout the region, as are the beautiful little flower-peckers (Dicæidæ), and some peculiar forms of weaver-birds (_Ploceus_ and _Munia_). Of the starling family, the most conspicuous are the glossy mynahs (_Eulabes_). The swallow-shrikes (_Artamus_) are very peculiar, as are the exquisitely coloured pittas (Pittidæ), and the gaudy broad-bills (Eurylæmidæ). Leaving the true Passeres, we find woodpeckers, barbets, and cuckoos everywhere, often of peculiar and {317}remarkable forms; among the bee-eaters we have the exquisite _Nyctiornis_ with its pendent neck-plumes of blue or scarlet; brilliant kingfishers and strangely formed hornbills abound everywhere; while brown-backed trogons with red and orange breasts, though far less frequent, are equally a feature of the Ornithology. Next we have the frog-mouthed goatsuckers (_Battrachostomus_), and the whiskered swifts (_Dendrochelidon_), both wide-spread, remarkable, and characteristic groups of the Oriental region. Coming to the parrot tribe, we have only the long-tailed _Palæornis_ and the exquisite little _Loriculus_, as characteristic genera. We now come to the pigeons, among which the fruit-eating genera _Treron_ and _Carpophaga_ are the most conspicuous. The gallinaceous birds offer us some grand forms, such as the peacocks (_Pavo_); the argus pheasants (_Argusianus_); the fire-backed pheasants (_Euplocamus_); and the jungle-fowl (_Gallus_), all strikingly characteristic; and with these we may close our sketch, since the birds of prey and the two Orders comprising the waders and swimmers offer nothing sufficiently remarkable to be worthy of enumeration here. _Reptiles._--Only the more abundant and characteristic groups will here be noticed. In the serpent tribe, the Oligodontidæ, a small family of ground-snakes; the Homalopsidæ, or fresh-water snakes; the Dendrophidæ, or tree-snakes; the Dryiophidæ, or whip-snakes; the Dipsadidæ, or nocturnal tree-snakes; the Lycodontidæ or fanged ground-snakes; the Pythonidæ, or rock-snakes; the Elapidæ, or venomous colubrine snakes (including the "cobras"); and the Crotalidæ, or pit-vipers, are all abundant and characteristic, ranging over nearly the whole region, and presenting a great variety of genera and species. Among lizards, the Varanidæ or water-lizards; the Scincidæ or "scinks;" the Geckotidæ, or geckoes; and the Agamidæ, or eastern iguanas; are the most universal and characteristic groups. Among crocodiles the genus _Crocodilus_ is widely spread, _Gavialis_ being characteristic of the Ganges. Among Chelonia, or shielded reptiles, forms of fresh-water Testudinidæ and Trionychidæ (soft tortoises) are tolerably abundant. _Amphibia._--The only abundant and characteristic groups of {318}this class are toads of the family Engystomidæ; tree-frogs of the family Polypedatidæ; and several genera of true frogs, Ranidæ. _Fresh-water Fishes._--The more remarkable and characteristic fishes inhabiting the fresh waters of the Oriental region belong to the following families: Nandidæ, Labyrinthici, Ophiocephalidæ, Siluridæ, and Cyprinidæ; the last being specially abundant. The sketch here very briefly given, must be supplemented by an examination of the tables of distribution of the genera of all the Mammalia and Birds inhabiting the region. We will now briefly summarize the results. _Summary of the Oriental Vertebrata._--The Oriental region possesses examples of 163 families of Vertebrata of which 12 are peculiar, a proportion of a little more than one-fourteenth of the whole. Out of 118 genera of Mammalia 54 seem to be peculiar to the region, equal to a proportion of 9/20 or a little less than half. Of Land-Birds there are 342 genera of which 165 are peculiar, bringing the proportion very close to a half. In the Ethiopian region the proportion of peculiar forms both of Mammalia and Birds is greater; a fact which is not surprising when we consider the long continued isolation of the latter region--an isolation which is even now very complete, owing to the vast extent of deserts intervening between it and the Palæarctic region; while the Oriental and Palæarctic were, during much of the Tertiary epoch, hardly separable. _Insects._ _Lepidoptera._--We can only glance hastily at the more prominent features of the wonderfully rich and varied butterfly-fauna of the Oriental region. In the first family Danaidæ, the genera _Danais_ and _Euploea_ are everywhere abundant, and the latter especially forms a conspicuous feature in the entomological aspect of the country; the large "spectre-butterflies" (_Hestia_) are equally characteristic of the Malayan sub-region. Satyridæ, though abundant are not very remarkable, _Debis_, _Melanitis_, _Mycalesis_, and _Ypthima_ being the most characteristic {319}genera. Morphidæ are well represented by the genera _Amathusia_, _Zeuxidia_, _Discophora_, and _Thaumantis_, some of the species of which almost equal the grand South American Morphos. The Nymphalidæ furnish us with a host of characteristic genera, among the most remarkable of which are, _Terinos_, _Adolias_, _Cethosia_, _Cyrestis_, _Limenitis_, and _Nymphalis_, all abounding in beautiful species. Among the Lycænidæ are a number of fine groups, among which we may mention _Ilerda_, _Myrina_, _Deudoryx_, _Aphneus_, _Iolaus_, and _Amblypodia_, as characteristic examples. The Pieridæ furnish many fine forms, such as _Thyca_, _Iphias_, _Thestias_, _Eronia_, _Prioneris_, and _Dercas_, the last two being peculiar. The Papilionidæ are unsurpassed in the world, presenting such grand genera as _Teinopalpus_ and _Bhutanitis_; the yellow-marked _Ornithopteræ_; the superb "Brookiana;" the elegant _Leptocercus_; and _Papilios_ of the "Coon," "Philoxenus," "Memnon," "Protenor," and especially the 'green-and-gold-dusted' "Paris" groups. The Moths call for no special observations, except to notice the existence in Northern India of a number of forms which resemble in a striking manner some of the most remarkable of the above mentioned groups of the genus _Papilio_, especially the "Protenor" group, which there is reason to believe protected by a peculiar smell or taste like the _Heliconias_ and Danaidæ. _Coleoptera._--The most characteristic Oriental form of the Cicindelidæ or tiger beetles, is undoubtedly the elegant genus _Collyris_, which is found over the whole region and is almost confined to it. Less abundant, but equally characteristic, is the wingless ant-like _Tricondyla_. Two small genera _Apteroessa_ and _Dromicidia_ are confined to the Indian Peninsula, while _Therates_ only occurs in the Malayan sub-region. The Carabidæ, or ground carnivorous beetles, are so numerous that we can only notice a few of the more remarkable and characteristic forms. The wonderful _Mormolyce_ of the Indo-Malay sub-region, stands pre-eminent for singularity in the entire family. _Thyreopterus_, _Orthogonius_, _Catascopus_, and _Pericallus_ are very characteristic forms, as well as _Planetes_ and {320}_Distrigus_, the latter having a single species in Madagascar. There are 80 genera of this family peculiar to the region, 10 of which have only been found in Ceylon. Among the Lucanidæ, or stag-beetles, _Lucanus_, _Odontolabris_, and _Cladognathus_ are the most characteristic forms. Sixteen genera inhabit the region, of which 7 are altogether peculiar, while three others only extend eastward to the Austro-Malayan sub-region. The beautiful Cetoniidæ, or rose-chafers, are well represented by _Rhomborhina_, _Heterorhina_, _Clinteria_, _Macronota_, _Agestrata_, _Chalcothea_ and many fine species of _Cetonia_. There are 17 peculiar genera, of which _Mycteristes_, _Phædimus_, _Plectrone_, and _Rhagopteryx_, are Malayan; while _Narycius_, _Clerota_, _Bombodes_, and _Chiloloba_ are Indian. In Buprestidæ--those elongate metallic-coloured beetles whose elytra are used as ornaments in many parts of the world--this region stands pre-eminent, in its gigantic _Catoxantha_, its fine _Chrysochroa_, its Indian _Sternocera_, its Malayan _Chalcophora_ and _Belionota_, as well as many other beautiful forms. It possesses 41 genera, of which 14 are peculiar to it, the rest being generally of wide range or common to the Ethiopian and Australian regions. In the extensive and elegant group of Longicorns, the Oriental region is only inferior to the Neotropical. It possesses 360 genera, 25 of which are Prionidæ, 117 Cerambicidæ, and 218 Lamiidæ;--about 70 per cent. of the whole being peculiar. The most characteristic genera are _Rhaphidopodus_ and _Ægosoma_ among Prionidæ; _Neocerambyx_, _Euryarthrum_, _Pachyteria_, _Acrocyrta_, _Tetraommatus_, _Chloridolum_, and _Polyzonus_ among Cerambycidæ; and _Coelosterna_, _Rhytidophora_, _Batocera_, _Agelasta_, and _Astathes_ among Lamiidæ. Of remarkable forms in other families, we may mention the gigantic horned _Chalcosoma_ among Scarabæidæ; the metallic _Campsosternus_ among Elateridæ; the handsome but anomalous _Trictenotoma_ forming a distinct family; the gorgeous _Pachyrhynchi_ of the Philippine Islands among Curculionidæ; _Diurus_ {321}among Brenthidæ; with an immense number and variety of Anthotribidæ, Heteromera, Malacoderma, and Phytophaga. THE ORIENTAL SUB-REGIONS. The four sub-regions into which we have divided the Oriental region, are very unequal in extent, and perhaps more so in productiveness, but they each have well-marked special features, and serve well to exhibit the main zoological characteristics of the region. As they are all tolerably well defined and their faunas comparatively well-known, their characteristics will be given with rather more than usual detail. _I. Hindostan, or Indian Sub-region._ This includes the whole peninsula of India from the foot of the Himalayas on the north to somewhere near Seringapatam on the south, the boundary of the Ceylonese sub-region being unsettled. The deltas of the Ganges and Brahmaputra mark its eastern limits, and it probably reaches to about Cashmere in the north-west, and perhaps to the valley of the Indus further south; but the great desert tract to the east of the Indus forms a transition to the south Palæarctic sub-region. Perhaps on the whole the Indus may be taken as a convenient boundary. Many Indian naturalists, especially Mr. Blyth and Mr. Blanford, are impressed with the relations of the greater part of this sub-region to the Ethiopian region, and have proposed to divide it into several zoological districts dependent on differences of climate and vegetation, and characterized by possessing faunas more or less allied either to the Himalayan or the Ethiopian type. But these subdivisions appear far too complex to be useful to the general student, and even were they proved to be natural, would be beyond the scope of this work. I agree, however, with Mr. Elwes in thinking that they really belong to local rather than to geographical distribution, and confound "station" with "habitat." Wherever there is a marked diversity of surface and vegetation the productions of a country will correspondingly differ; the groups peculiar to forests, for example, will be absent from open {322}plains or arid deserts. It happens that the three great Old World regions are separated from each other by a debatable land which is chiefly of a desert character; hence we must expect to find a resemblance between the inhabitants of such districts in each region. We also find a great resemblance between the aquatic birds of the three regions; and as we generally give little weight to these in our estimate of the degree of affinity of the faunas of different countries, so we should not count the desert fauna as of equal weight with the more restricted and peculiar types which are found in the fertile tracts,--in the mountains and valleys, and especially in the primeval forests. The supposed preponderance of exclusively Ethiopian groups of Mammalia and Birds in this, sub-region, deserves however a close examination, in order to ascertain how far the facts really warrant such an opinion. _Mammalia._--The following list of the more important genera of Mammalia which range over the larger part of this sub-region will enable naturalists to form an independent judgment as to the preponderance of Ethiopian, or of Oriental and Palæarctic types, in this, the most important of all the classes of animals for geographical distribution. RANGE OF THE GENERA OF MAMMALIA WHICH INHABIT THE SUB-REGION OF HINDOSTAN. 1. Presbytes Oriental only. 2. Macacus Oriental only. 3. Erinaceus Palæarctic genus. 4. Sorex Widely distributed. 5. Felis Almost Cosmopolitan. 6. Cynælurus Ethiopian and S. Palæarctic. 7. Viverra Ethiopian and Oriental to China and Malaya. 8. Viverricula Oriental only. 9. Paradoxurus Oriental only. 10. Herpestes Ethiopian, S. Palæarctic, and Oriental to Malaya. 11. Calogale Ethiopian, Oriental to Cambodja. 12. Tæniogale Oriental. 13. Hyæna Palæarctic and Ethiopian (a Palæarctic species.) 14. Canis Palæarctic and Oriental to Malaya. 15. Cuon Oriental to Malaya. 16. Vulpes Very wide range. 17. Lutra Oriental and Palæarctic. 18. Mellivora Ethiopian. 19. Melursus Oriental only; family not Ethiopian. 20. Sus Palæarctic and Oriental, not Ethiopian. 21. Tragulus Oriental. {323} 22. Cervus Oriental and Palæarctic; family not Ethiopian. 23. Cervulus Oriental; family not Ethiopian. 24. Bibos Palæarctic and Oriental. 25. Portax Oriental. 26. Gazella Palæarctic and Ethiopian. 27. Antilope Oriental. 28. Tetraceros Oriental. 29. Elephas Oriental species. 30. Mus Cosmopolite nearly. 31. Platacanthomys Oriental. 32. Meriones Very wide range. 33. Spalacomys Oriental. 34. Sciurus Almost Cosmopolite. 35. Pteromys Palæarctic and Oriental to China and Malaya, 36. Hystrix Wide range. 37. Lepus Wide range. 38. Manis Ethiopian and Oriental to Malaya, Out of the above 38 genera, 8 have so wide a distribution as to give no special geographical indications. Of the remaining 30, whose geographical position we have noted, 14 are Oriental only; 5 have as much right to be considered Oriental as Ethiopian, extending as they do over the greater part of the Oriental region; 2 (the hyæna and gazelle) show Palæarctic rather than Ethiopian affinity; 7 are Palæarctic and Oriental but not Ethiopian; and only 2 (_Cynælurus_ and _Mellivora_) can be considered as especially Ethiopian. We must also give due weight to the fact that we have here Ursidæ and Cervidæ, two families entirely absent from the Ethiopian region, and we shall then be forced to conclude that the affinities of the Indian peninsula are not only clearly Oriental, but that the Ethiopian element is really present in a far less degree than the Palæarctic. _Birds._--The naturalists who have adopted the "Ethiopian theory" of the fauna of Hindostan, have always supported their views by an appeal to the class of birds; maintaining, that not only are almost all the characteristic Himalayan and Malayan genera absent, but that their place is to a great extent supplied by others which are characteristic of the Ethiopian region. After a careful examination of the subject, Mr. Elwes, in a paper read before the Zoological Society (June 1873) came to the conclusion, that this view was an erroneous one, founded on the fact that the birds of the plains are the more abundant and more {324}open to observation; and that these are often of wide-spread types, and some few almost exclusively African. The facts he adduced do not, however, seem to have satisfied the objectors; and as the subject is an important one, I will here give lists of all the genera of Passeres, Picariæ, Psittaci, Columbæ, and Gallinæ, which inhabit the sub-region, leaving out those which only just enter within its boundaries from adjacent sub-regions. These are arranged under four heads:--1. Oriental genera; which are either wholly confined to, or strikingly prevalent in, the Oriental region beyond the limits of the Indian peninsula. 2. Genera of Wide Range; which are fully as much entitled to be considered Oriental or Palæarctic as Ethiopian, and cannot be held to prove any Ethiopian affinity. 3. Palæarctic genera; which are altogether or almost absent from the Ethiopian region. 4. Ethiopian genera; which are confined to, or very prevalent in, the Ethiopian region, whence they extend into the Indian peninsula but not over the whole Oriental region. The last are the only ones which can be fairly balanced against those of the first list, in order to determine the character of the fauna. 1. ORIENTAL GENERA IN CENTRAL INDIA. _Geocichla_, _Orthotomus_, _Prinia_, _Megalurus_, _Abrornis_, _Larvivora_, _Copsychus_, _Kittacincla_, _Pomatorhinus_, _Malacocercus_, _Chatarrhæa_, _Layardia_, _Garrulax_, _Trochalopteron_, _Pellorneum_, _Dumetia_, _Pyctoris_, _Alcippe_, _Myiophonus_, _Sitta_, _Dendrophila_, _Phyllornis_, _Iora_, _Hypsipetes_, _Pericrocotus_, _Graucalus_, _Volvocivora_, _Chibia_, _Chaptia_, _Irena_, _Erythrosterna_, _Hemipus_, _Hemichelidon_, _Niltava_, _Cyornis_, _Eumyias_, _Hypothymis_, _Myialestes_, _Tephrodornis_, _Dendrocitta_, _Arachnechthra_, _Nectarophila_, _Arachnothera_, _Dicæum_, _Piprisoma_, _Munia_, _Eulabes_, _Pastor_, _Acridotheres_, _Sturnia_, _Sturnopastor_, _Artamus_, _Nemoricola_, _Pitta_, _Yungipicus_, _Chrysocolaptes_, _Hemicircus_, _Gecinus_, _Mulleripicus_, _Brachypternus_, _Tiga_, _Micropternus_, _Megalæma_, _Xantholæma_, _Rhopodytes_, _Taccocoua_, _Surniculus_, _Hierococcyx_, _Eudynamnis_, _Nyctiornis_, _Harpactes_, _Pelargopsis_, _Ceyx_, _Hydrocissa_, _Meniceros_, _Batrachostomus_, _Dendrochelidon_, _Collocalia_, _Palæornis_, _Treron_, _Carpophaga_, _Chalcophaps_, _Ortygornis_, _Perdix_, _Pavo_, _Gallus_, _Galloperdix_;--87 genera; and {325}one peculiar genus, _Salpornis_, whose affinities are Palæarctic or Oriental. 2. GENERA OF WIDE RANGE OCCURRING IN CENTRAL INDIA. _Tardus_, _Monticola_, _Drymoeca_, _Cisticola_, _Acrocephalus_, _Phylloscopus_, _Pratincola_, _Parus_, _Pycnonotus_, _Criniger_, _Oriolus_, _Dicrurus_, _Tchitrea_, _Lanius_, _Corvus_, _Zosterops_, _Hirundo_, _Cotyle_, _Passer_, _Ploceus_, _Estrilda_, _Alauda_, _Calandrella_, _Mirafra_, _Ammomanes_, _Motacilla_, _Anthus_, _Picus_, _Yunx_, _Centropus_, _Cuculus_, _Chrysoccocyx_, _Coccystes_, _Coracias_, _Eurystomus_, _Merops_, _Alcedo_, _Ceryle_, _Halcyon_, _Upupa_, _Caprimulgus_, _Cypselus_, _Chætura_, _Columba_, _Turtur_, _Pterocles_, _Coturnix_, _Turnix_;--48 genera. 3. PALÆARCTIC GENERA OCCURRING IN CENTRAL INDIA. _Hypolais_, _Sylvia_, _Curruca_, _Cyanecula_, _Calliope_, _Chelidon_, _Euspiza_, _Emberiza_, _Galerita_, _Calobates_, _Corydalla_;--11 genera. 4. ETHIOPIAN GENERA OCCURRING IN CENTRAL INDIA. _Thamnobia_, _Pyrrhulauda_, _Pterocles_, _Francolinus_;--4 genera. A consideration of the above lists shows us, that the Hindostan sub-region is by no means so poor in forms of bird-life as is generally supposed (and as I had myself anticipated, it would prove to be), possessing, as it does, 151 genera of land-birds, without counting the Accipitres. It must also set at rest the question of the zoological affinities of the district, since a preponderance of 88 genera, against 4, cannot be held to be insufficient, and cannot be materially altered by any corrections in details that may be proposed or substantiated. Even of these four, only the first two are exclusively Ethiopian, _Pterocles_ and _Francolinus_ both being Palæarctic also. It is a question, indeed, whether anywhere in the world an outlying sub-region can be found, exhibiting less zoological affinity for the adjacent regions; and we have here a striking illustration of the necessity of deciding all such cases, not by _examples_, which may be so chosen as to support any view, but by carefully weighing and contrasting the whole of the facts on which the solution of the {326}problem admittedly depends. It will, perhaps, be said that a great many of the 88 genera above given are very scarce and very local; but this is certainly not the case with the majority of them; and even where it is so, that does not in any degree affect their value as indicating zoo-geographical affinities. It is the _presence_ of a type in a region, not its abundance or scarcity, that is the important fact; and when we have to do, as we have here, with many groups whose habits and mode of life necessarily seclude them from observation, their supposed scarcity may not even be a fact. _Reptiles and Amphibia._--Reptiles entirely agree with Mammalia and Birds in the main features of their distribution. Out of 17 families of snakes inhabiting Hindostan, 16 range over the greater part of the entire region, and only two can be supposed to show any Ethiopian affinity. These are the Psammophidæ and Erycidæ, both desert-haunting groups, and almost as much South Palæarctic as African. The genus _Tropidococcyx_ is peculiar to the sub-region, and _Aspidura_, _Passerita_ and _Cynophis_ to the peninsula and Ceylon; while a large number of the most characteristic genera, as _Dipsas_, _Simotes_, _Bungarus_, _Naja_, _Trimeresurus_, _Lycodon_ and _Python_, are characteristically Oriental. Of the six families of lizards all have a wide range. The genera _Eumeces_, _Pentadactylus_, _Gecko_, _Eublepharis_, and _Draco_, are characteristically or wholly Oriental; _Ophiops_ and _Uromastix_ are Palæarctic; while _Chamæleon_ is the solitary case of decided Ethiopian affinity. Of the Amphibia not a single family exhibits special Ethiopian affinities. _II. Sub-region of Ceylon and South-India._ The Island of Ceylon is characterised by such striking peculiarities in its animal productions, as to render necessary its separation from the peninsula of India as a sub-region; but it is found that most of these special features extend to the Neilgherries and the whole southern mountainous portion of India, and that the two must be united in any zoo-geographical {327}province. The main features of this division are,--the appearance of numerous animals allied to forms only found again in the Himalayas or in the Malayan sub-region, the possession of several peculiar generic types, and an unusual number of peculiar species. _Mammalia._--Among Mammalia the most remarkable form is _Loris_, a genus of Lemurs altogether peculiar to the sub-region; several peculiar monkeys of the genus _Presbytes_; the Malayan genus _Tupaia_; and _Platacanthomys_, a peculiar genus of Muridæ. _Birds._--Among birds it has _Ochromela_, a peculiar genus of flycatchers; _Phoenicophaës_ (Cuculidæ) and _Drymocataphus_ (Timaliidæ), both Malayan forms; a species of _Myiophonus_ whose nearest ally is in Java; _Trochalopteron_, _Brachypteryx_, _Buceros_ and _Loriculus_, which are only found elsewhere in the Himalayas and Malayana. It also possesses about 80 peculiar species of birds, including a large jungle fowl, one owl and two hornbills. _Reptiles._--It is however by its Reptiles, even more than by its higher vertebrates, that this sub-region is clearly characterised. Among snakes it possesses an entire family, Uropeltidæ, consisting of 5 genera and 18 species altogether confined to it,--_Rhinophis_ and _Uropeltis_ in Ceylon, _Silybura_, _Plecturus_ and _Melanophidium_ in Southern India. Four other genera of snakes, _Haplocercus_, _Cercaspis_, _Peltopelor_, and _Hypnale_ are also peculiar; _Chersydrus_ is only found elsewhere in Malaya; while _Aspidura_, _Passerita_, and _Cynophis_, only extend to Hindostan; and species of _Eryx_, _Echis_, and _Psammophis_ show an affinity with Ethiopian and Palæarctic forms. Among lizards several genera of _Agamidæ_ are peculiar, such as _Otocryptis_, _Lyricoephalus_, _Ceratophora_, _Cophotis_, _Salea_, _Sitana_ and _Charasia_. In the family Acontiadæ, _Nessia_ is peculiar to Ceylon, while a species of the African genus _Acontias_ shows an affinity for the Ethiopian region. _Amphibia._--The genera of Amphibians that occur here are generally of wide range, but _Nannophrys_, _Haplobatrachus_, and _Cacopus_ are confined to the sub-region; while _Megalophrys_ is Malayan, and the species found in Ceylon also inhabit Java. {328}_Insects._--The insects of Ceylon also furnish some curious examples of its distinctness from Hindostan, and its affinity with Malaya. Among its butterflies we find _Papilio jophon_, closely allied to _P. antiphus_ of Malaya. The remarkable genus _Hestia_, so characteristic of the Malay archipelago, only occurs elsewhere on the mountains of Ceylon; while its _Cynthia_ and _Parthenos_ are closely allied to, if not identical with, Malayan species. Among Coleoptera we have yet more striking examples. The highly characteristic Malayan genus _Tricondyla_ is represented in Ceylon by no less than 10 species; and among Longicorns we find the genera _Tetraommatus_, _Thranius_, _Cacia_, _Praonetha_, _Ropica_, and _Serixia_, all exclusively Malayan or only just entering the Indo-Chinese peninsula, yet all represented in Ceylon, while not a single species occurs in any part of India or the Himalayas. _The Past History of Ceylon and South-India as indicated by its Fauna._--In our account of the Ethiopian region we have already had occasion to refer to an ancient connection between this sub-region and Madagascar, in order to explain the distribution of the Lemurine type, and some other curious affinities between the two countries. This view is supported by the geology of India, which shows us Ceylon and South India consisting mainly of granitic and old metamorphic rocks, while the greater part of the peninsula, forming our first sub-region, is of tertiary formation, with a few isolated patches of secondary rocks. It is evident therefore, that during much of the tertiary period, Ceylon and South India were bounded on the north by a considerable extent of sea, and probably formed part of an extensive southern continent or great island. The very numerous and remarkable cases of affinity with Malaya, require however some closer approximation to these islands, which probably occurred at a later period. When, still later, the great plains and table-lands of Hindostan were formed, and a permanent land communication effected with the rich and highly developed Himalo-Chinese fauna, a rapid immigration of new types took place, and many of the less specialised forms of mammalia and birds (particularly those of ancient Ethiopian type) became extinct. Among reptiles and insects the competition was less severe, or the older forms were too well {329}adapted to local conditions to be expelled; so that it is among these groups alone that we find any considerable number, of what are probably the remains of the ancient fauna of a now submerged southern continent. _III. Himalayan or Indo-Chinese Sub-region._ This, which is probably the richest of all the sub-regions, and perhaps one of the richest of all tracts of equal extent on the face of the globe, is essentially a forest-covered, mountainous country, mostly within the tropics, but on its northern margin extending some degrees beyond it, and rising in a continuous mountain range till it meets and intercalates with the Manchurian sub-division of the Palæarctic region. The peculiar mammalia, birds and insects of this sub-region begin to appear at the very foot of the Himalayas, but Dr. Gunther has shown that many of the reptiles characteristic of the plains of India are found to a height of from 2,000 to 4,000 feet. In Sikhim, which may be taken as a typical example of the Himalayan portion of the sub-region, it seems to extend to an altitude of little less than 10,000 feet, that being the limit of the characteristic Timaliidæ or babbling thrushes; while the equally characteristic Pycnonotidæ, or bulbuls, and Treronidæ, or thick-billed fruit-pigeons, do not, according to Mr. Blanford, reach quite so high. We may perhaps take 9,000 feet as a good approximation over a large part of the Himalayan range; but it is evidently not possible to define the line with any great precision. Westward, the sub-region extends in diminishing breadth, till it terminates in or near Cashmere, where the fauna of the plains of India almost meets that of the Palæarctic region, at a moderate elevation. Eastward, it reaches into East Thibet and North-west China, where Père David has found a large number of the peculiar types of the Eastern Himalayas. A fauna, in general features identical, extends over Burmah and Siam to South China; mingling with the Palæarctic fauna in the mountains south of the Yang-tse-kiang river, and with that of Indo-Malaya in Tenasserim, and to a lesser extent in Southern Siam and Cochin China. {330}_Zoological Characteristics of the Himalayan Sub-region._--Taking this sub-region as a whole, we find it to be characterised by 3 genera of mammalia (without counting bats), and 44 genera of land-birds, which are altogether peculiar to it; and by 13 genera of mammalia and 36 of birds, which it possesses in common with the Malayan sub-region; and besides these it has almost all the genera before enumerated as "Oriental," and several others of wide range, more especially a number of Palæarctic genera which appear in the higher Himalayas. The names of the more characteristic genera are as follows:-- PECULIAR HIMALO-CHINESE GENERA. Mammalia.--_Urva_, _Arctonyx_, _Ælurus_. Birds.--_Suya_, _Horites_, _Chæmarrhornis_, _Tarsiger_, _Oreicola_, _Acanthoptila_, _Grammatoptila_, _Trochalopteron_, _Actinodura_, _Sibia_, _Suthora_, _Paradoxornis_, _Chlenasicus_, _Tesia_, _Rimator_, _Ægithaliscus_, _Cephalopyrus_, _Liothrix_, _Siva_, _Minla_, _Proparus_, _Cutia_, _Yuhina_, _Ixulus_, _Myzornis_, _Erpornis_, _Hemixus_, _Chibia_, _Niltava_, _Anthipes_, _Chelidorhynx_, _Urocissa_, _Pachyglossa_, _Heterura_, _Hæmatospiza_, _Ampeliceps_, _Saroglossa_, _Psarisomus_, _Serilophus_, _Vivia_, _Hyopicus_, _Gecinulus_, _Aceros_, _Ceriornis_. GENERA COMMON TO THE HIMALO-CHINESE AND MALAYAN SUB-REGIONS. Mammalia.--_Hylobates_, _Nycticebus_, _Viverricula_, _Prionodon_, _Arctitis_, _Paguma_, _Arctogale_, _Cuon_, _Gymnopus_, _Aonyx_, _Helictis_, _Rhinoceros_, _Nemorhedus_, _Rhizomys_. Birds.--_Oreocincla_, _Notodela_, _Janthocincla_, _Timalia_, _Stachyris_, _Mixornis_, _Trichastoma_, _Enicurus_, _Pnoepyga_, _Melanochlora_, _Allotrius_, _Microscelis_, _Iole_, _Analcipus_, _Cochoa_, _Bhringa_, _Xanthopygia_, _Hylocharis_, _Cissa_, _Temnurus_, _Crypsirhina_, _Chalcostetha_, _Anthreptes_, _Chalcoparia_, _Cymbirhynchus_, _Hydrornis_, _Sasia_, _Venilia_, _Indicator_, _Carcineutes_, _Lyncornis_, _Macropygia_, _Argusianus_, _Polyplectron_, _Euplocamus_, _Phodilus_. Plate VII. [Illustration] SCENE IN NEPAUL, WITH CHARACTERISTIC ANIMALS. {331}_Plate VII. Scene in Nepal, with Characteristic Himalayan Animals._--Our illustration contains figures of two mammals and two birds, characteristic of the higher woody region of the Himalayas. The lower figure on the left is the _Helictis nepalensis_, confined to the Eastern Himalayas, and belonging to a genus of the weasel family which is exclusively Oriental. It is marked with white on a grey-brown ground. Above it is the remarkable Panda (_Ælurus fulgens_), a beautiful animal with a glossy fur of a reddish colour, darker feet, and a white somewhat cat-like face. It is distantly allied to the bears, and more nearly to the American racoons, yet with sufficient differences to constitute it a distinct family. The large bird on the tree, is the horned Tragopan (_Ceriornis satyra_), one of the fine Himalayan pheasants, magnificently spotted with red and white, and ornamented with fleshy erectile wattles and horns, of vivid blue and red colours. The bird in the foreground is the _Ibidorhynchus struthersii_, a rare and curious wader, allied to the curlews and sandpipers but having the bill and feet red. It frequents the river-beds in the higher Himalayas, but has also been found in Thibet. _Reptiles._--Very few genera of reptiles are peculiar to this sub-region, all the more important ranging into the Malay islands. Of snakes the following are the more characteristic genera:--_Typhline_, _Cylindrophis_, _Xenopeltis_, _Calamaria_, _Xenelaphis_, _Hypsirhina_, _Fordonia_, several small genera of Homalopsidæ (_Herpeton_ and _Hipistes_ being characteristic of Burmah and Siam), _Psammodynastes_, _Gonyosoma_, _Chrysopelea_, _Tragops_, _Dipsas_, _Pareas_, _Python_, _Bungarus_, _Naja_, _Callophis_, and _Trimeresurus_. _Naja_ reaches 8,000 feet elevation in the Himalayas, _Tropidonotus_ 9,000 feet, _Ablabes_ 10,000 feet, and _Simotes_ 15,000 feet. Of lizards, _Pseudopus_ has one species in the Khasya hills while the other inhabits South-east Europe; and there are two small genera of Agamidæ peculiar to the Himalayas, while _Draco_ and _Calotes_ have a wide range and _Acanthosaura_, _Dilophyrus_, _Physignathus_, and _Liolepis_ are found chiefly in the Indo-Chinese peninsula. There are several genera of Scincidæ; and the extensive genus of wall-lizards, _Gecko_, ranges over the whole region. Of Amphibia, the peculiar forms are not numerous. _Ichthyophis_ {332}a genus of Ceciliadæ, is peculiar to the Khasya Hills; _Tylotritron_ (Salamandridæ) to Yunan in Western China, and perhaps belongs to the Palæarctic region. Of the tail-less Batrachians, _Glyphoglossus_ is found in Pegu; _Xenophys_ in the Eastern Himalayas; while _Callula_, _Ixalus_, _Rhacophorus_, _Hylurana_, _Oxyglossus_, and _Phrynoglossus_, are common to the Himalo-Chinese and Malayan sub-regions. Of the lizards, _Colotes_, _Barycephalus_, and _Hinulia_,--and of the Batrachia, _Bufo_,--are found at above 11,000 feet elevation in the Himalayas. _Insects._--So little has been done in working out the insect faunas of the separate sub-regions, that they cannot be treated in detail, and the reader is referred to the chapter on the distribution of insects in the part of this work devoted to Geographical Zoology. A few particulars may, however, be given as to the butterflies, which have been more systematically collected in tropical countries than any other order of insects. The Himalayan butterflies, especially in the eastern portions of the range--in Assam and the Khasya Hills--are remarkably fine and very abundant; yet all the larger groups extend into the Malayan sub-region, many to Ceylon, and a considerable proportion even to Africa and Austro-Malaya. There are a large number of peculiar types, but most of them consist of few or single species. Such are _Neope_, _Orenoma_, and _Rhaphicera_, genera of Satyridæ; _Enispe_ (Morphidæ); _Hestina_, _Penthema_, and _Abrota_ (Nymphalidæ); _Dodona_ (Erycinidæ); _Ilerda_ (Lycænidæ); _Calinaga_, _Teinopalpus_, and _Bhutanitis_ (Papilionidæ). Its more prominent features are, however, derived from what may be termed Malayan, or even Old World types, such as _Euplæa_, among Danaidæ; _Amathusia_, _Clerome_, and _Thaumantis_, among Morphidæ; _Euripus_, _Diadema_, _Athyma_, _Limenitis_, and _Adolias_, among Nymphalidæ; _Zemeros_ and _Taxila_ among Erycinidæ; _Amblypodia_, _Miletus_, _Ilerda_, and _Myrina_, among Lycænidæ; _Thyca_, _Prioneris_, _Dercas_, _Iphias_, and _Thestias_ among Pieridæ; and Papilios of the "_Amphrisius_," "_Coon_", "_Philoxenus_," "_Protenor_," "_Paris_," and "_Sarpedon_" groups. In the Himalayas there is an unusual abundance of large and gorgeous species of the genus _Papilio_, {333}and of large and showy Nymphalidæ, Morphidæ, and Danaidæ, which render it, in favoured localities, only second to South America for a display of this form of beauty and variety in insect life. Among the other orders of insects in which the Himalayas are remarkably rich, we may mention large and brilliant Cetoniidæ, chiefly of the genus _Rhomborhima_; a magnificent Lamellicorn, _Euchirus macleayii_, allied to the gigantic long-armed beetle (_E. longimanus_) of Amboyna; superb moths of the families Agaristidæ and Sesiidæ; elegant and remarkable Fulgoridæ, and strange forms of the gigantic Phasmidæ; most of which appear to be of larger size or of more brilliant colours than their Malayan allies. _Islands of the Indo-Chinese Sub-region._--A few important islands belong to this sub-region, the Andamans, Formosa, and Hainan being the most interesting. _Andamans._--The only mammalia are a few rats and mice, a _Paradoxurus_, and a pig supposed to be a hybrid race,--all of which may have been introduced by man's agency. The birds of the Andaman Islands have been largely collected, no less than 155 species having been obtained; and of these 17, (all land-birds) are peculiar. The genera are all found on the continent, and are mostly characteristic of the Indo-Chinese fauna, to which most of the species belong. Reptiles are also tolerably abundant; about 20 species are known, the majority being found also on the continent, while a few are peculiar. There are also a few Batrachia, and some fresh-water fishes, closely resembling those of Burmah. The absence of such mammalia as monkeys and squirrels, which abound on the mainland, and which are easily carried over straits or narrow seas by floating trees, is sufficient proof that these islands have not recently formed part of the continent. The birds are mostly such as may have reached the islands while in their present geographical position; and the occurrence of reptiles and fresh-water fishes, said to be identical in species with those of Burmah, must be due to the facilities, which some of these animals undoubtedly {334}possess, for passing over a considerable width of sea. We must conclude, therefore, that these islands do not owe their existing fauna to an actual union with the mainland; but it is probable that they may have been formerly more extensive, and have then been less distant from the continent than at the present time. The Nicobar Islands, usually associated with the Andamans, are less known, but present somewhat similar phenomena. They are, however, more Malayan in their fauna, and seem properly to belong to the Indo-Malay sub-region. _Formosa._--This island has been carefully examined by Mr. Swinhoe, who found 144 species of birds, of which 34 are peculiar. There is one peculiar genus, but the rest are all Indo-Chinese, though some of the species are more allied to Malayan than to Chinese or Himalayan forms. About 30 species of mammalia were found in Formosa, of which 11 are peculiar species, the rest being either Chinese or Himalayan. The peculiar species belong to the genera _Talpa_, _Helictis_, _Sciuropterus_, _Pteromys_, _Mus_, _Sus_, _Cervus_, and _Capricornis_. A few lizards and snakes of continental species have also been found. These facts clearly indicate the former connection of Formosa with China and Malaya, a connection which is rendered the more probable by the shallow sea which still connects all these countries. _Hainan._--The island of Hainan, on the south coast of China, is not so well known in proportion, though Mr. Swinhoe collected 172 species of birds, of which 130 were land-birds. Of these about 20 were peculiar species; the remainder being either Chinese, Himalayan, or Indo-Malayan. Mr. Swinhoe also obtained 24 species of mammalia, all being Chinese, Himalayan, or Indo-Malayan species except a hare, which is peculiar. This assemblage of animals would imply that Hainan, as might be anticipated from its position, has been more recently separated from the continent than the more distant island of Formosa. _IV. Indo-Malaya, or the Malayan Sub-region._ This sub-region, which is almost wholly insular (including only the Malayan peninsula on the continent of Asia), is equal, if {335}not superior, in the variety and beauty of its productions, to that which we have just been considering. Like Indo-China, it is a region of forests, but it is more exclusively tropical; and it is therefore deficient in many of those curious forms of the temperate zone of the Himalayas, which seem to have been developed from Palæarctic rather than from Oriental types. Here alone, in the Oriental region, are found the most typical equatorial forms of life--organisms adapted to a climate characterised by uniform but not excessive heat, abundant moisture, and no marked departure from the average meteorological state, throughout the year. These favourable conditions of life only occur in three widely separated districts of the globe--the Malay archipelago, Western Africa, and equatorial South America. Hence perhaps it is, that the tapir and the trogons of Malacca should so closely resemble those of South America; and that the great anthropoid apes and crested hornbills of Western Africa, should find their nearest allies in Borneo and Sumatra. Although the islands which go to form this sub-region are often separated from each other by a considerable expanse of sea, yet their productions in general offer no greater differences than those of portions of the Indo-Chinese sub-region separated by an equal extent of dry land. The explanation is easy, however, when we find that the sea which separates them is a very shallow one, so shallow that an elevation of only 300 feet would unite Sumatra, Java, and Borneo into one great South-eastern prolongation of the Asiatic continent. As we know that our own country has been elevated and depressed to a greater amount than this, at least twice in recent geological times, we can have no difficulty in admitting similar changes of level in the Malay archipelago, where the subterranean forces which bring about such changes are still at work, as manifested by the great chain of active volcanoes in Sumatra and Java. Proofs of somewhat earlier changes of level are to be seen in the Tertiary coal formations of Borneo, which demonstrate a succession of elevations and subsidences, with as much certainty as if we had historical record of them. It is not necessary to suppose, nor is it probable, that all these {336}great islands were recently united to the continent, and that their separation took place by one general subsidence of the whole. It is more consonant with what we know of such matters, that the elevations and depressions were partial, varying in their points of action and often recurring; sometimes extending one part of an island, sometimes another; now joining an island to the main land, now bringing two islands into closer proximity. There is reason to believe that sometimes an intervening island has sunk or receded and allowed others which it before separated to effect a partial union independently of it. If we recognise the probability that such varied and often-renewed changes of level have occurred, we shall be better able to understand how certain anomalies of distribution in these islands may have been brought about. We will now endeavour to sketch the general features of the zoology of this interesting district, and then proceed to discuss some of the relations of the islands to each other. _Mammalia._--We have seen that the Indo-Chinese sub-region possesses 13 species of mammalia in common with the Indo-Malay sub-region, and 4 others peculiar to itself, besides one Ethiopian and several Oriental and Palæarctic forms of wide range. Of this latter class the Malay islands have comparatively few, but they possess no less than 14 peculiar genera, viz. _Simia_, _Siamanga_, _Tarsius_, _Galeopithecus_, _Hylomys_, _Ptilocerus_, _Gymnura_, _Cynogale_, _Hemigalea_, _Arctogale_, _Barangia_, _Mydaus_, _Helarctos_, and _Tapirus_. The islands also possess tigers, deer, wild pigs, wild cattle, elephants, the scaly ant-eater, and most of the usual Oriental genera; so that they are on the whole fully as rich as, if not richer than, any part of Asia; a fact very unusual in island faunas, and very suggestive of their really continental nature. Plate VIII. [Illustration] A FOREST IN BORNEO, WITH CHARACTERISTIC MAMMALIA. {337}_Plate VIII. Scene in Borneo with Characteristic Malayan Quadrupeds._--The Malayan fauna is so rich and peculiar that we devote two plates to illustrate it. We have here a group of mammalia, such as might be seen together in the vast forests of Borneo. In the foreground we have the beautiful deer-like Chevrotain (_Tragulus javanicus_). These are delicate little animals whose body is not larger than a rabbit's, thence often called "mouse-deer." They were formerly classed with the "musk-deer," owing to their similar tusk-like upper canines; but their anatomy shows them to form quite a distinct family, having more resemblance to the camels. On the branch above is the curious feather-tailed Tree-Shrew (_Ptilocerus lowii_), a small insectivorous animal altogether peculiar to Borneo. Above this is the strange little Tarsier (_Tarsius spectrum_), one of the lemurs confined to the Malay islands, but so distinct from all others as to constitute a separate family. The other small animals are the Flying Lemurs (_Galæopithecus volans_) formerly classed with the lemurs, but now considered to belong to the Insectivora. They have a very large expansion of the skin connecting the fore and hind limbs and tail, and are able to take long flights from one tree to another, and even to rise over obstacles in their course by the elevatory power of the tail-membrane. They feed chiefly on leaves, and have a very soft and beautifully marbled fur. In the distance is the Malayan tapir (_Tapirus indicus_), a representative of a group of animals now confined to the larger Malay islands and tropical America, but which once ranged over the greater part of temperate Europe. _Birds._--Owing to several of the families consisting of very obscure and closely allied species, which have never been critically examined and compared by a competent ornithologist, the number of birds inhabiting this sub-region is uncertain. From the best available materials there appear to be somewhat less than 650 species of land-birds actually known, or excluding the Philippine Islands somewhat less than 600. The larger part of these are peculiar species, but mostly allied to those of Indo-China; 36 of the genera, as already stated, being common to these two sub-regions. There are, however, no less than 46 genera which are peculiarly or wholly Indo Malayan and, in many cases, have no close affinity with other Oriental groups. These peculiar genera are as follows:--_Timalia_, _Malacopteron_, _Macronus_, _Napothera_, _Turdinus_, and _Trichixos_--genera {338}of Timaliidæ; _Eupetes_, a most remarkable form, perhaps allied to _Enicurus_, and _Cinclus_; _Rhabdornis_ (Certhiidæ) found only in the Philippines; _Psaltria_, a diminutive bird of doubtful affinities, provisionally classed among the tits (Paridæ); _Setornis_ (Pycnonotidæ); _Lalage_ (Campephagidæ) extending eastward to the Pacific Islands; _Pycnosphrys_, _Philentoma_ (Muscicapidæ); _Laniellus_, a beautiful bird doubtfully classed with the shrikes (Laniidæ); _Platylophus_ and _Pityriasis_, the latter a most anomalous form--perhaps a distinct family, at present classed with the jays, in Corvidæ; _Prionochilus_, a curious form classed with Dicæidæ; _Erythrura_ (Ploceidæ), extending eastwards to the Fiji Islands; _Gymnops_, _Calornis_, (Sturnidæ); _Eurylæmus_, _Corydon_, and _Calyptomena_ (Eurylæmidæ); _Eucichla_, the longest tailed and most elegantly marked of the Pittidæ; _Reinwardtipicus_ and _Miglyptes_ (Picidæ); _Psilopogon_ and _Calorhamphus_, (Megalæmidæ); _Rhinococcyx_, _Dasylophus_, _Lepidogrammus_, _Carpococcyx_, _Zanclostomus_, _Poliococcyx_, _Rhinortha_, (Cuculidæ); _Berenicornis_, _Caldo_, _Cranorhinus_, _Penelopides_, _Rhinoplax_, (Bucerotidæ); _Psittinus_, (Psittacidæ); _Ptilopus_, _Phapitreron_, (Columbidæ); _Rollulus_, (Treronidæ); _Machærhamphus_, (Falconidæ). Many of these genera are abundant and wide-spread, while some of the most characteristic Himalayan genera, such as _Larvivora_, _Garrulax_, _Hypsipetes_, _Pomatorhinus_, and _Dendrocitta_, are here represented by only a few species. Among the groups that are characteristic of the Malayan sub-region, the Timaliidæ and Pycnonotidæ stand pre-eminent; the former represented chiefly by the genera _Timalia_, _Malacopteron_, _Macronus_, and _Trichastoma_, the latter by _Criniger_, _Microscelis_, and many forms of _Pycnonotus_. The Muscicapidæ, Dicruridæ, Campephagidæ, Ploceidæ, and Nectariniidæ are also well developed; as well as the Pittidæ, and the Eurylæmidæ, the limited number of species of the latter being compensated by a tolerable abundance of individuals. Among the Picariæ are many conspicuous groups; as, woodpeckers (Picidæ); barbets (Megalæmidæ); trogons (Trogonidæ); kingfishers (Alcedinidæ); and hornbills (Bucerotidæ); five families which are perhaps the most conspicuous in the whole fauna. Lastly come the pigeons {339}(Columbidæ), and the pheasants (Phasianidæ), which are fairly represented by such fine genera as _Treron_, _Ptilopus_, _Euplocamus_, and _Argusianus_. A few forms whose affinities are Australian rather than Oriental, help to give a character to the ornithology, though none of them are numerous. The swallow-shrikes (_Artamus_); the wag-tail fly-catchers (_Rhipidura_); the green fruit-doves (_Ptilopus_); and the mound-makers (_Megapodius_), are the chief of these. There are a few curious examples of remote geographical alliances that may be noted. First, we have a direct African connection in _Machærhamphus_, a genus of hawks, and _Berenicornis_, a genus of hornbills; the only close allies being, in the former case in South, and in the latter in West Africa. Then we have a curious Neotropical affinity, indicated by _Carpococcyx_, a large Bornean ground-cuckoo, whose nearest ally is the genus _Neomorphus_ of South America; and by the lovely green-coloured _Calyptomena_ which seems unmistakably allied to the orange-coloured _Rupicola_, or "Cock of the rock," in general structure and in the remarkable form of crest, a resemblance which has been noticed by many writers. In the preceding enumeration of Malayan genera several are included which extend into the Austro-Malay Islands, our object, at present, being to show the differences and relations of the two chief Oriental sub-regions. _Plate IX. A Malayan Forest with some of its peculiar Birds._--Our second illustration of the Malayan fauna is devoted to its bird-life; and for this purpose we place our scene in the Malay peninsula, where birds are perhaps more abundant and more interesting, than in any other part of the sub-region. Conspicuous in the foreground is the huge Rhinoceros Hornbill (_Buceros rhinoceros_), one of the most characteristic birds of the Malayan forests, the flapping of whose wings, as it violently beats the air to support its heavy body, may be heard a mile off. On the ground behind, is the Argus pheasant (_Argusianus giganteus_) whose beautifully ocellated wings have been the subject of a most interesting description in Mr. Darwin's _Descent of Man_. The wing-feathers are here so enormously {340}developed for display (as shown in our figure) that they become almost, if not quite, useless for their original purpose of flight; yet the colours are so sober, harmonizing completely with the surrounding vegetation, and the bird is so wary, that in the forests where it abounds an old hunter assured me he had never been able to see a specimen till it was caught in his snares. It is interesting to note, that during the display of the plumage the bird's head is concealed by the wings from a spectator in front, and, contrary to what usually obtains among pheasants, the head is entirely unadorned, having neither crest nor a particle of vivid colour,--a remarkable confirmation of Mr. Darwin's views, that gayly coloured plumes are developed in the male bird for the purpose of attractive display in the breeding season. The long-tailed bird on the right is one of the Drongo-shrikes (_Bhringa remifer_), whose long bare tail-feathers, with an oar-like web at the end, and blue-black glossy plumage, render it a very attractive object as it flies after its insect prey. On the left is another singular bird the great Broad-bill (_Corydon sumatranus_), with dull and sombre plumage, but with a beak more like that of a boat-bill than of a fruit-eating passerine bird. Over all, the white-handed Gibbon (_Hylobates lar_) swings and gambols among the topmost branches of the forest. _Reptiles and Amphibia._--These are not sufficiently known to be of much use for our present purpose. Most of the genera belong to the continental parts of the Oriental region, or have a wide range. Of snakes _Rhabdosoma_, _Typhlocalamus_, _Tetragonosoma_, _Acrochordus_, and _Atropos_, are the most peculiar, and there are several peculiar genera of Homalopsidæ. Of Oriental genera, _Cylindrophis_, _Xenopeltes_, _Calamaria_, _Hypsirhina_, _Psammodynastes_, _Gonyosoma_, _Tragops_, _Dipsas_, _Pareas_, _Python_, _Bungarus_, _Naja_, and _Callophis_ are abundant; as well as _Simotes_, _Ablabes_, _Tropidonotus_, and _Dendrophis_, which are widely distributed. Among lizards _Hydrosaurus_ and _Gecko_ are common; there are many isolated groups of Scincidæ; while _Draco_, _Calotes_, and many forms of Agamidæ, some of which are peculiar, abound. Plate IX. [Illustration] A MALAYAN FOREST, WITH ITS CHARACTERISTIC BIRDS. {341}Among the Amphibia, toads and frogs of the genera _Micrhyla_, _Kalophrynus_, _Ansonia_, and _Pseudobufo_, are peculiar: while the Oriental _Megalophrys_, _Ixalus_, _Rhacophorus_, and _Hylorana_ are abundant and characteristic. _Fishes._--The fresh-water fishes of the Malay archipelago have been so well collected and examined by the Dutch naturalists, that they offer valuable indications of zoo-geographical affinity; and they particularly well exhibit the sharply defined limits of the region, a large number of Oriental and even Ethiopian genera extending eastward as far as Java and Borneo, but very rarely indeed sending a single species further east, to Celebes or the Moluccas. Thirteen families of fresh-water fishes are found in the Indo-Malay sub-region. Of these the Scienidæ and Symbranchidæ have mostly a wide range in the tropics. Ophiocephalidæ are exclusively Oriental, reaching Borneo and the Philippine islands. The Mastacembelidæ are also Oriental, but one species is found as far as Ceram. Of the Nandidæ, 3 genera range over the whole region. The Labyrinthici extend from Africa through the Oriental region to Amboyna, The single species constituting the family Luciocephalidæ is confined to Borneo and the small islands of Biliton and Banca. Of the extensive family Siluridæ 17 genera are Oriental and Malayan, and 11 are Malayan exclusively; and not one of these appears to pass beyond the limits of the sub-region. The Cyprinidæ offer an equally striking example, 23 genera ranging eastward to Java and Borneo and not one beyond; 14 of these being exclusively Malayan. It must be remembered that this is not from any want of knowledge of the countries farther east, as extensive collections have also been made in Celebes, the Moluccas, and Timor; so that the facts of distribution of fresh-water fishes come, most unexpectedly, to fortify that division of the archipelago into two primary regions, which was founded on a consideration of mammalia and birds only. _Insects._--Few countries in the world can present a richer and more varied series of insects than the Indo-Malay islands, and we can only here notice a few of their more striking peculiarities and more salient features. {342}The butterflies of this sub-region, according to the best estimate that can be formed, amount to about 650 described species, a number that will yet, no doubt, be very considerably increased. The genera which appear to be peculiar to it are _Erites_ (Satyridæ); _Zeuxidia_ (Morphidæ); _Amnosia_, _Xanthotænia_, and _Tanæcia_ (Nymphalidæ). The groups which are most characteristic of the region, either from their abundance in individuals or species, or from their size and beauty, are--the rich dark-coloured _Euplæa_; the large semi-transparent _Hestia_; the plain-coloured _Mycalesis_, which replace our meadow-brown butterflies (_Hipparchia_); the curious _Elymnias_, which often closely resemble Euplæas; the large and handsome _Thamantis_ and _Zeuxidia_, which take the place of the giant Morphos of South America; the _Cethosia_, of the brightest red, and marked with a curious zigzag pattern; the velvety and blue-glossed _Terinos_; the pale and delicately-streaked _Cyrestis_; the thick-bodied and boldly coloured _Adolias_; the small wine-coloured _Taxila_; the fine blue _Amblypodia_; the beautiful _Thyca_, elegantly marked underneath with red and yellow, which represent our common white butterflies and are almost equally abundant; the pale blue _Eronia_, and the large red-tipped _Iphias_. The genus _Papilio_ is represented by a variety of fine groups; the large _Ornithoptera_, with satiny yellow under-wings; the superb green-marked "_brookeana_;" the "_paradoxa_" group, often closely resembling the Euplæas that abound in the same district; the "_paris_" group richly dusted with golden-green specks; the "_helenus_" group with wide-spreading black and white wings; the black and crimson "_polydorus_" group; the "_memnon_" group, of the largest size and richly-varied colours; and the "_eurypilus_" group, elegantly banded or spotted with blue or green: all these are so abundant that some of them are met with in every walk, and are a constant delight to the naturalist who has the privilege of observing them in their native haunts. The Coleoptera are far less prominent and require to be carefully sought after; but they then well repay the collector. As affording some measure of the productiveness of the tropics in insect life it will not be out of place to give a few notes of the {343}number of species collected by myself in some of the best localities. At Singapore 300 species of Coleoptera were collected in 15 days, and in a month the number had increased to 520; of which 100 were Longicorns and 140 Rhyncophora. At Sarawak in Borneo I obtained 400 species in 15 days, and 600 in a month. In two months this number had increased to about 850, and in three months to 1,000 species. This was the most prolific spot I ever collected in, especially for Longicorns which formed about one-fifth of all the species of beetles. In the Aru Islands in one month, I obtained only 235 species of Coleoptera, and about 600 species of insects of all orders; and this may be taken as a fair average, in localities where no specially favourable conditions existed. On the average 40 to 60 species of Coleoptera would be a good day's collecting; 70 exceptionally good; while the largest number ever obtained in one day was 95, and the majority of these would be very minute insects. It must be remembered, however, that many very common species were passed over, yet had every species met with been collected, not much more than 100 species would ever have been obtained in one day's collecting of four or five hours. These details may afford an interesting standard of comparison for collectors in other parts of the world. Of Cicindelidæ the most peculiarly Malayan form is _Therates_, found always on leaves in the forests in the same localities as the more widely spread _Collyris_. Five genera of this family are Indo-Malayan. The Carabidæ, though sufficiently plentiful, are mostly of small size, and not conspicuous in any way. But there is one striking exception in the purely Malayan genus _Mormolyce_, the largest and most remarkable of the whole family. It is nocturnal, resting during the days on the under side of large _boleti_ in the virgin forest. _Pericallus_ and _Catascopus_ are among the few genera which are at all brillantly coloured. Buprestidæ are abundant, and very gay; the genus _Belionota_ being perhaps one of the most conspicuous and characteristic. The giant _Catoxantha_ is, however, the most peculiar, though comparatively scarce. _Chrysochroa_ and _Chalcophora_ are also {344}abundant and characteristic. Out of the 41 Oriental genera 21 are Malayan, and 10 of these are not found in the other sub-regions. In Lucanidæ the Malay islands are rich, 14 out of the 16 Oriental genera occurring there, and 3 being peculiar. There are many fine species of _Odontolabris_, which may be considered the characteristic genus of the sub-region. The Cetoniidæ are well represented by 16 genera and about 120 species. The genera _Mycteristes_, _Phædimus_, _Plectrone_, _Euremina_, _Rhagopteryx_ and _Centrognathus_ are peculiar, while _Agestrata_, _Chalcothea_, and _Macronota_ are abundant and characteristic. The Longicorns, as in all continental forest regions near the equator, are very abundant and in endlessly varied forms. No less than 55 genera containing about 200 species are peculiar to this sub-region, the Cerambycidæ being much the most numerous. _Euryarthrum_, _Coelosterna_, _Agelasta_, and _Astathes_ may be considered as most characteristic; but to name the curious and interesting forms would be to give a list of half the genera. For the relations of the Longicorns of the Indo-Malay, and those of the Austro-Malay region, the reader is referred to the chapter on the distribution of insects in the succeeding part of this work. _Terrestrial Mollusca._--The Philippine islands are celebrated as being one of the richest parts of the world for land shells, about 400 species being known. The other islands of the sub-region are far less rich, not more than about 100 species having yet been described from the whole of them. _Helix_ and _Bulimus_ both abound in species in the Philippines, whereas the latter genus is very scarce in Borneo and Java. Ten genera of Helicidæ inhabit the sub-region; _Pfeifferia_ is found in the Philippines and Moluccas, while the large genus _Cochlostyla_ is almost peculiar to the Philippines. Of the Operculata there are representatives of 20 genera, of which _Dermatoma_ and _Pupinella_ are peculiar, while _Registoma_ and _Callia_ extend to the Australian region. _Cyclophorus_, _Leptopoma_, and _Pupina_ are perhaps the most characteristic genera. {345}_The Zoological Relations of the Several Islands of the Indo-Malay Sub-region._ Although we have grouped the Philippine islands with the Indo-Malay sub-region, to which, as we shall see, they undoubtedly belong, yet most of the zoological characteristics we have just sketched out, apply more especially to the other groups of islands and the Malay peninsula. The Philippine islands stand, to Malaya proper, in the same relation that Madagascar does to Africa or the Antilles to South America; that is, they are remarkable for the absence of whole families and genera which everywhere characterise the remainder of the district. They are, in fact, truly insular, while the other islands are really continental in all the essential features of their natural history. Before, therefore, we can conveniently compare the separate islands of Malaya[12] with each other, we must first deal with the Philippine group, showing in what its speciality consists, and why it must be considered apart from the sub-region to which it belongs. _Mammals of the Philippine Islands._--The only mammalia recorded as inhabiting the Philippine Islands are the following:-- QUADRUMANA. 1. Macacus cynomolgus. 2. Cynopithecus niger. Dr. Semper doubts this being a Philippine species. LEMUROIDEA. 3. Tarsius spectrum. INSECTIVORA. 4. Galeopithecus philippinensis. 5. Tupaia (species). On Dr. Semper's authority. CARNIVORA. 6. Viverra tangalunga. 7. Paradoxurus philippensis. UNGULATA. 8. Sus (species). On Dr. Semper's authority. 9. Cervus mariannus. 10. Cervus philippensis. 11. Cervus alfredi. 12. Bos (species). Wild cattle; perhaps introduced. RODENTIA. 13. Phlæomys cummingii. 14. Scuirus philippinensis. Also 24 species, belonging to 17 genera, of bats. {346}The foregoing list, although small, contains an assemblage of species which are wholly Oriental in character, and several of which (_Tarsius_, _Galeopithecus_, _Tupaia_) are characteristic and highly peculiar Malayan forms. At the same time these islands are completely separated from the rest of Malaya by the total absence of _Semnopithecus_, _Hylobates_, _Felis_, _Helarctos_, _Rhinoceros_, _Manis_, and other groups constantly found in the great Indo-Malay islands and peninsula of Malacca. We find apparently two sets of animals: a more ancient series, represented by the deer, _Galeopithecus_, and squirrel, in which the species are distinct from any others; and a more recent series, represented by _Macacus cynomolgus_, and _Viverra tangalunga_, identical with common Malayan animals. The former indicate the earliest period when these volcanic islands were connected with some part of the Malayan sub-region, and they show that this was not geologically remote, since no peculiar generic types have been preserved or differentiated. The latter may indicate either the termination of the period of union, or merely the effects of introduction by man. The reason why a larger number of mammalian forms were not introduced and established, was probably because the union was effected only with some small islands, and from these communicated to other parts of the archipelago; or it may well be that later subsidences extinguished some of the forms that had established themselves. _Birds of the Philippine Islands._--These have been carefully investigated by Viscount Walden, in a paper read before the Zoological Society of London in 1873, and we are thus furnished with ample information on the relations of this important portion of the fauna. The total number of birds known to inhabit the Philippines is 219, of which 106 are peculiar. If, however, following our usual plan, we take only the land-birds, we find the numbers to be 159 species, of which 100 are peculiar; an unusually large proportion for a group of islands so comparatively near to various parts of the Oriental and Australian regions. The families of birds which are more especially characteristic of the Indo-Malay sub-region are about 28 in number, and examples {347}of all these are found in the Philippines except four, viz., Cinclidæ, Phyllornithidæ, Eurylæmidæ, and Podargidæ. The only Philippine families which are, otherwise, exclusively Austro-Malayan are, Cacatuidæ and Megapodiidæ. Yet although the birds are unmistakably Malayan, as a whole, there are, as in the mammalia (though in a less degree), marked deficiencies of most characteristic Malayan forms. Lord Walden gives a list of no less than 69 genera thus absent; but it will be sufficient here to mention such wide-spread and specially Indo-Malay groups as,--_Eurylæmus_, _Nyctiornis_, _Arachnothera_, _Geocichla_, _Malacopteron_, _Timalia_, _Pomatorhinus_, _Phyllornis_, _Iora_, _Criniger_, _Enicurus_, _Chaptia_, _Tchitrea_, _Dendrocitta_, _Eulabes_, _Palæornis_, _Miglyptes_, _Tiga_, and _Euplocamus_. These deficiencies plainly show the isolated character of the Philippine group, and imply that it has never formed a part of that Indo-Malayan extension of the continent which almost certainly existed when the peculiar Malayan fauna was developed; or that, if it has been so united, it has been subsequently submerged and broken up to such an extent, as to cause the extinction of many of the absent types. It appears from Lord Walden's careful analysis, that 31 of the Philippine species occur in the Papuan sub-region, and 47 in Celebes; 69 occur also in India, and 75 in Java. This last fact is curious, since Java is the most remote of the Malayan islands, but it is found to arise almost wholly from the birds of that island being better known, since only one species, _Xantholæma rosea_, is confined to the Philippine Islands and Java. The wading and swimming birds are mostly of wide-spread forms, only 6 out of the 60 species being peculiar to the Philippine archipelago. Confining ourselves to the land-birds, and combining several of the minutely subdivided genera of Lord Walden's paper so as to agree with the arrangement adopted in this work, we find that there are 112 genera of land-birds represented in the islands. Of these, 50 are either cosmopolitan, of wide range, or common to the Oriental and Australian regions, and may be put aside as affording few indications of geographical affinity. Of the remaining 62 no less than 40 are exclusively {348}or mainly Oriental, and most of them are genera which range widely over the region, only two (_Philentoma_ and _Rollulus_) being exclusively Malayan, and two others (_Megalurus_ and _Malacocircus_) more especially Indian or continental. Five other genera, though having a wide range, are typically Palæarctic, and have reached the islands through North China. They are, _Monticola_, _Acrocephalus_, _Phylloscopus_, _Calliope_, and _Passer_; the two first having extended their range southward into the Moluccas. The peculiarly Australian genera are only 12, the majority being characteristic Papuan and Moluccan forms; such as--_Campephaga_, _Alcyone_, _Cacatua_, _Tanygnathus_, _Ptilopus_, _Janthænas_, _<Phlogænas_, and _Megapodius_. One is peculiar to Celebes (_Prioniturus_); one to the Papuan group (_Cyclopsitta_); and one is chiefly Australian (_Gerygone_). The beautiful little parroquets forming the genus _Loriculus_, are characteristic of the Philippines, which possess 5 species, a larger number than occurs in any other group of islands, though they range from India to New Guinea. There remain six peculiar genera--_Rhabdornis_, an isolated form of creepers (Certhiidæ); _Gymnops_, a remarkable bareheaded bird belonging to the starlings (Sturnidæ); _Dasylophus_, and _Lepidogrammus_, remarkable genera of cuckoos (Cuculidæ); _Penelopides_, a peculiar hornbill, and _Phapitreron_, a genus of pigeons. Besides these there are four other types (here classed as sub-genera, but considered to be distinct by Lord Walden) which are peculiar to the Philippines. These are _Pseudoptynx_, an owl of the genus _Athene_; _Pseudolalage_, a sub-genus of _Lalage_; _Zeocephus_, a sub-genus of _Tchitrea_; and _Ptilocolpa_, included under _Carpophaga_. When we look at the position of the Philippine group, connected by the Bashee islands with Formosa, by Palawan and the Sooloo archipelago with Borneo, and by the Tulour and other islets with the Moluccas and Celebes, we have little difficulty in accounting for the peculiarities of its bird fauna. The absence of a large number of Malayan groups would indicate that the actual connection with Borneo, which seems necessary for the introduction of the Malay types of mammalia, was not of long duration; while the large proportion of wide-spread continental genera of birds would seem to imply that greater facilities had {349}once existed for immigration from Southern China, perhaps by a land connection through Formosa, at which time the ancestors of the peculiar forms of deer entered the country. It may indeed be objected that our knowledge of these islands is far too imperfect to arrive at any satisfactory conclusions as to their former history; but although many more species no doubt remain to be discovered, experience shows that the broad characters of a fauna are always determined by a series of collections made by different persons, at various localities, and at different times, even when more imperfect than those of the Philippine birds really are. The isolated position, and the volcanic structure of the group, would lead us to expect them to be somewhat less productive than the Moluccas, close to the rich and varied Papuan district,--or than Celebes, with its numerous indications of an extensive area and great antiquity; and taking into account the excessive poverty of its mammalian fauna, which is certain to be pretty well known, I am inclined to believe that no future discoveries will materially alter the character of Philippine ornithology, as determined from the materials already at our command. _Java._--Following the same plan as we have adopted in first discussing the Philippine islands, and separating them from the body of the sub-region on account of special peculiarities, we must next take Java, as possessing marked individuality, and as being to some extent more isolated in its productions than the remaining great islands. Java is well supplied with indigenous mammalia, possessing as nearly as can be ascertained 55 genera and 90 species. None of these genera are peculiar, and only about 5 of the species,--3 quadrumana, a deer and a wild pig. So far then there is nothing remarkable in its fauna, but on comparing it with that of the other great islands, viz., Borneo and Sumatra, and the Malay peninsula, we find an unmistakable deficiency of characteristic forms, the same in kind as that we have just commented on in the case of the Philippines, though much less in degree. First, taking genera which are found in all three of the above-named {350}localities and which must therefore be held to be typical Malayan groups, the following are absent from Java: _Viverra_, _Gymnopus_, _Lutra_, _Helarctos_, _Tapirus_, _Elephas_, and _Gymnura_; while of those _known_ to occur in two, and which, owing to our imperfect knowledge, may very probably one day be discovered in the third, the following are equally wanting: _Simia_, _Siamanga_, _Hemigalea_, _Paguma_, _Rhinosciurus_, and _Rhizomys_. It may be said this is only negative evidence, but in the case of Java it is much more, because this island is not only the best known of any in the archipelago, but there is perhaps no portion of British India of equal extent so well known. It is one of the oldest of the Dutch possessions and the seat of their colonial government; good roads traverse it in every direction, and experienced naturalists have been resident in various parts of it for years together, and have visited every mountain and every forest, aided by bands of diligent native collectors. We should be almost as likely to find new species of mammalia in Central Europe as in Java; and therefore the absence of such animals as the Malay bear, the elephant, tapir, gymnura, and even less conspicuous forms, must be accepted as a positive fact. In the other islands there are still vast tracts of forest in the hands of natives and utterly unexplored, and any similar absence in their case will prove little; yet on making the same comparison in the case of Borneo, the most peculiar and the least known of the other portions of the sub-region, we find only 2 genera absent which are found in the three other divisions, and only 3 which are found in two others. A fact to be noted also is, that the only genus found in Java but not in other parts of the sub-region (_Helictis_) occurs again in North India; and that some Javan _species_, as _Rhinoceros javanicus_, and _Lepus kurgosa_ occur again in the Indo-Chinese sub-region, but not in the Malayan. Among the birds we meet with facts of a similar import; and though the absence of certain types from Java is not quite so certain as among the mammalia, this is more than balanced by the increased number of such deficiencies, so that if a few {351}should be proved to be erroneous, the main result will remain unaltered. Java possesses about 270 species of land birds, of which about 40 are peculiar to it. There are, however, very few peculiar genera, _Laniellus_, a beautiful spotted shrike, being the most distinct, while _Cochoa_ and _Psaltria_ are perhaps not different from their Indian allies. The island has however a marked individuality in two ways--in the absence of characteristic Malayan types, and in the presence of a number of forms not yet found in any of the other Malay islands, but having their nearest allies in various parts of the Indo-Chinese sub-region. The following 16 genera are all found in Malacca, Sumatra, and Borneo, but are absent from Java: _Setornis_, _Temnurus_, _Dendrocitta_, _Corydon_, _Calyptomena_, _Venilia_, _Reinwardtipicus_, _Caloramphus_, _Rhinortha_, _Nyctiornis_, _Cranorhinus_, _Psittinus_, _Polyplectron_, _Argusianus_, _Euplocamus_, and _Rollulus_. The following 9 are known from _two_ of the above localities, and will very probably be found in the third, but are absent from, and not likely to occur in, Java: _Trichixos_, _Eupetes_, _Melanochlora_, _Chaptia_, _Pityriasis_, _Lyncornis_, _Carpococcyx_, _Poliococcyx_, and _Rhinoplax_. We have thus 25 typically Malayan genera which are not known to occur in Java. The following genera, on the other hand, do not occur in any of the Malayan sub-divisions except Java, and they all occur again, or under closely allied forms, in the Indo-Chinese sub-region; _Brachypteryx_ (allied species in Himalayas); _Zoothera_ (allied species in Aracan); _Notodela_ (allied species in Pegu); _Pnoëpyga_ (allied species in Himalayas); _Allotrius_ (allied species in the Himalayas); _Cochoa_ (allied species in the Himalayas); _Crypsirhina_ (allied species in Burmah); _Estrilda_ (allied species in India); _Psaltria_ (allied genus--_Ægithaliscus_--in Himalayas); _Pavo muticus_ and _Harpactes oreskios_ (same species in Siam and Burmah); _Cecropis striolata_ (same species in Java and Formosa, and allied species in India). Here we have 12 instances of very remarkable distribution, and considering that there are nearly as many birds known from Sumatra and Borneo as from Java, and considerably more from {352}the Malay peninsula, it is not likely that many of these well marked forms will be discovered in these countries. There are also a considerable number of species of birds common to Malacca, Sumatra, and Borneo, but represented in Java by distinct though closely allied species. Such are,-- _Venilia malaccensis_ (represented in Java by) _V. miniata_. _Drymocataphus nigrocapitatus_ " " _D. capistratus_. _Malacopteron coronatum_ " " _M. rufifrons_. _Irena cyanea_ " " _I. turcosa_. _Ploceus baya_ " " _P. hypoxantha_. _Loriculus galgulus_ " " _L. pusillus_. _Ptilopus jambu_ " " _P. porphyreus_. Now if we look at our map of the region, and consider the position of Java with regard to Borneo, Sumatra, and the Indo-Chinese peninsula, the facts just pointed out appear most anomalous and perplexing. First, we have Java and Sumatra forming one continuous line of volcanoes, separated by a very narrow strait, and with all the appearance of having formed one continuous land; yet their productions differ considerably, and those of Sumatra show the closest resemblance to those of Borneo, an island ten times further off than Java and differing widely in the absence of volcanoes or any continuous range of lofty mountains. Then again, not only does Java differ from these two, but it agrees with a country beyond them both--a country from which they seem to have a much better chance to have been supplied by immigration than Java has, and to have (almost necessarily) participated, even more largely, in the benefits of any means of transmission capable of reaching the latter island. Yet more; whatever changes have occurred to bring about the anomalous state of things that exists must have been, zoologically and geologically, recent; for the strange cross-affinities between Java and the Indo-Chinese continent (in which Sumatra and Borneo have not participated), as well as that between Malacca, Sumatra, and Borneo (in which Java has not participated) are exhibited, in many cases by community of _species_, in others by the presence of very closely allied forms of the same _genera_, of mammalia and birds. Now we know that {353}these higher animals become replaced by allied species much more rapidly than the mollusca; and it is also pretty certain that the modification by which this replacement is effected takes place more rapidly when the two sets of individuals are isolated from each other, and especially when they are restricted to islands, where they are necessarily subject to distinct and pretty constant conditions, both physical and organic. It becomes therefore almost a certainty, that Siam and Java on the one hand, and Sumatra, Borneo, and Malacca on the other must have been brought into some close connexion, not earlier than the newer Pliocene period; but while the one set of countries were having their meeting, the other must have been by some means got out of the way. Before attempting to indicate the mode by which this might have been effected in accordance with what we know of the physical geography, geology, and vegetation of the several islands, it will be as well to complete our sketch of their zoological relations to each other, so as ascertain with some precision, what are the facts of distribution which we have to explain. _Malacca, Sumatra, and Borneo._--After having set apart the Philippine Islands and Java, we have remaining two great islands and a peninsula, which, though separated by considerable arms of the sea, possess a fauna of wonderful uniformity having all the typical Malayan features in their full development. Their unity is indeed so complete, that we can find hardly any groups of sufficient importance by which to differentiate them from each other; and we feel no confidence that future discoveries may not take away what speciality they possess. One after another, species or genera once peculiar to Borneo or Sumatra have been found elsewhere; and this has gone to such an extent in birds, that hardly a peculiar genus and very few peculiar species are left in either island. Borneo however is undoubtedly the most peculiar. It possesses three genera of Mammalia not found elsewhere; _Cynogale_, a curious carnivore allied to the otters; with _Dendrogale_ and _Ptilocerus_, small insectivora allied to _Tupaia_. It has _Simia_, the {354}Orang-utan, and _Paguma_, one of the Viverridæ, in common with Sumatra; as well as _Rhinosciurus_, a peculiar form of squirrel, and _Hemigalea_, one of the Viverridæ, in common with Malacca. Sumatra has only one genus not found in any other Malayan district--_Nemorhedus_, a form of antelope which occurs again in North India. It also has _Siamanga_ in common with Malacca, _Mydaus_ with Java, and _Rhizomys_ with India. The Malay Peninsula seems to have no peculiar forms of Mammalia, though it is rich in all the characteristic Malay types. The bats of the various islands have been very unequally collected, 36 species being recorded from Java, 23 from Sumatra, but only 16 each from Borneo and Malacca. Leaving these out of consideration, and taking into account the terrestrial mammals only, we find that Java is the poorest in species, while Borneo, Sumatra, and Malacca are tolerably equal; the numbers being 55, 62, 66, and 65 respectively. Of these we find that the species confined to each island or district are (in the same order) 6, 16, 5, and 6. It thus appears that Borneo is, in its mammalia, the most isolated and peculiar; next comes Sumatra, and then Malacca and Java, as shown by the following table. Peculiar Peculiar Genera. Species. Borneo 4 16 Sumatra 1 5 Malacca 0 6 Java 0 6 This result differs from that which we have arrived at by the more detailed consideration of the fauna of Java; and it serves to show that the estimate of a country by the number of its peculiar genera and species alone, may not always represent its true zoological importance or its most marked features. Java, as we have seen, is differentiated from the other three districts by the absence of numerous types common to them all, and by its independent continental relations. Borneo is also well distinguished by its peculiar genera and specific types, yet it is at the same time more closely related to Sumatra and Malacca than is Java. The two islands have evidently had a very different history, which a detailed knowledge of their geology {355}would alone enable us to trace. Should we ever arrive at a fair knowledge of the physical changes that have resulted in the present condition, we shall almost certainly find that many of the differences and anomalies of their existing fauna and flora will be accounted for. In Birds we hardly find anything to differentiate Borneo and Sumatra in any clear manner. _Pityriasis_ and _Carpococcyx_, once thought peculiar to the former, are now found also in the latter; and we have not a single genus left to characterize Borneo except _Schwaneria_ a peculiar fly-catcher, and _Indicator_, an African and Indian group not known to occur elsewhere in the Malay sub-region. Sumatra as yet alone possesses _Psilopogon_, a remarkable form of barbet, but we may well expect that it will be soon found in the interior of Borneo or Malacca; it also has _Berenicornis_, an African form of hornbill. The Malay Peninsula appears to have no genus peculiar to it, but it possesses some Chinese and Indian forms which do not pass into the islands. As to the species, our knowledge of them is at present very imperfect. The Malay Peninsula is perhaps the best known, but it is probable that both Sumatra and Borneo are quite as rich in species. With the exception of the genera noted above, and two or three others as yet found in two islands only, the three districts we are now considering may be said to have an almost identical bird-fauna, consisting largely of the same species and almost wholly of these together with closely allied species of the same genera. There are no well-marked groups which especially characterise one of these islands rather than the other, so that even the amount of speciality which Borneo undoubtedly exhibits as regards mammalia, is only faintly shown by its birds. The Pittidæ may perhaps be named as the most characteristic Bornean group, that island possessing six species, three of which are peculiar to it and are among the most beautiful birds of an unusually beautiful family. Yet Sumatra possesses two peculiar, and hardly less remarkable species. In other classes of vertebrates, in insects, and in land-shells, our knowledge is far too imperfect to allow of our making any useful comparison between the faunas. {356}_Banca._--We must, however note the fact of peculiar species occurring in Banca, a small island close to Sumatra, and thus offering another problem in distribution. A squirrel (_Sciurus bangkanus_) is allied to three species found in Malacca, Sumatra, and Borneo respectively, but quite as distinct from them all as they are from each other. More curious are the two species of _Pitta_ peculiar to Banca; one, _Pitta megarhynchus_, is allied to the _P. brachyurus_, which inhabits the whole sub-region and extends to Siam and China, but differs from it in its very large bill and differently coloured head; the other, _P. bangkanus_, is allied to _P. cucullatus_, which extends from Nepal to Malacca, and to _P. sordidus_, which inhabits both Borneo and Sumatra as well as the Philippines. We have here, on a small scale, a somewhat similar problem to that of Java, and as this is comparatively easy of solution we will consider it first. Although, on the map, Banca is so very close to Sumatra, the observer on the spot at once sees that the proximity has been recently brought about. The whole south-east coast of Sumatra is a great alluvial plain, hardly yet raised above the sea level, and half flooded in the wet season. It is plainly a recent formation, caused by the washing down into a shallow sea of the _débris_ from the grand range of volcanic mountains 150 miles distant. Banca, on the other hand is, though low, a rugged and hilly island, formed almost wholly of ancient rocks of apparently volcanic origin, and closely resembling parts of the Malay Peninsula and the intervening chain of small islands. There is every appearance that Banca once formed the extremity of the Peninsula, at which time it would probably have been separated from Sumatra by 50 or 100 miles of sea. Its productions should, therefore, most resemble those of Singapore and Malacca, and the few peculiar species it possesses will be due to their isolation in a small tract of country, surrounded by a limited number of animal and vegetable forms, and subject to the influence of a peculiar soil and climate. The parent species existing in such large tracts as Borneo or Sumatra, subjected to more varied conditions of soil, climate, vegetation, food, and enemies, would preserve, almost or quite {357}unchanged, the characteristics which had been developed under nearly identical conditions when the great island formed part of the continent. Geology teaches us that similar changes in the forms of the higher vertebrates have taken place during the Post-Tertiary epoch; and there are other reasons for believing that, under such conditions of isolation as in Banca, the change may have required but a very moderate period, even reckoned in years. We will now return to the more difficult problem presented by the peculiar continental relations of Java, as already detailed. _Probable Recent Geographical Changes in the Indo-Malay Islands._--Although Borneo is by far the largest of the Indo-Malay islands, yet its physical conformation is such that, were a depression to occur of one or two thousand feet, it would be reduced to a smaller continuous area than either Sumatra or Java. Except in its northern portion it possesses no lofty mountains, while alluvial valleys of great extent penetrate far into its interior. A very moderate depression, of perhaps 500 feet, would convert it into an island shaped something like Celebes; and its mountains are of so small an average elevation, and consist so much of isolated hills and detached ranges, that a depression of 2,000 feet would almost certainly break it up into a group of small islands, with a somewhat larger one to the north. Sumatra (and to a less extent Java) consists of an almost continuous range of lofty mountains, connected by plateaus from 3,000 to 4,000 feet high; so that although a depression of 2,000 feet would greatly diminish their size, it would probably leave the former a single island, while the latter would be separated into two principal islands of still considerable extent. The enormous amount of volcanic action in these two islands, and the great number of conical mountains which must have been slowly raised, chiefly by ejected matter, to the height of 10,000 and 12,000 feet, and whose shape indicates that they have been formed above water, renders it almost certain that for long periods they have not undergone submersion to any considerable extent. In Borneo, however, we have no such evidences. No volcano, {358}active or extinct, is known in its entire area; while extensive beds of coal of tertiary age, in every part of it, prove that it has been subject to repeated submersions, at no distant date geologically. An indication, if not a proof, of still more recent submersion is to be found in the great alluvial valleys which on the south and south-west extend fully 200 miles inland, while they are to a less degree a characteristic feature all round the island. These swampy plains have been formed by the combined action of rivers and tides; and they point clearly to an immediately preceding state of things, when that which is even now barely raised above the ocean, was more or less sunk below it. These various indications enable us to claim, as an admissible and even probable supposition, that at some epoch during the Pliocene period of geology, Borneo, as we now know it, did not exist; but was represented by a mountainous island at its present northern extremity, with perhaps a few smaller islets to the south. We thus have a clear opening from Java to the Siamese Peninsula; and as the whole of that sea is less than 100 fathoms deep, there is no difficulty in supposing an elevation of land connecting the two together, quite independent of Borneo on the one hand and Sumatra on the other. This union did not probably last long; but it was sufficient to allow of the introduction into Java of the _Rhinoceros javanicus_, and that group of Indo-Chinese and Himalayan species of mammalia and birds which it alone possesses. When this ridge had disappeared by subsidence, the next elevation occurred a little more to the east, and produced the union of many islets which, aided by sub-aerial denudation, formed the present island of Borneo. It is probable that this elevation was sufficiently extensive to unite Borneo for a time with the Malay Peninsula and Sumatra, thus helping to produce that close resemblance of genera and even of species, which these countries exhibit, and obliterating much of their former speciality, of which, however, we have still some traces in the long-nosed monkey and _Ptilocerus_ of Borneo, and the considerable number of genera both of mammalia and birds confined to two only out of the three divisions of typical Malaya. The subsidence which again divided these {359}countries by arms of the sea rather wider than at present, might have left Banca isolated, as already referred to, with its proportion of the common fauna to be, in a few instances, subsequently modified. Thus we are enabled to understand how the special relations of the _species_ of these islands to each other may have been brought about. To account for their more deep-seated and general zoological features, we must go farther back. _Probable Origin of the Malayan Fauna._--The typical Malayan fauna is essentially an equatorial one, and must have been elaborated in an extensive equatorial area. This ancient land almost certainly extended northward over the shallow sea as far as the island of Palawan, the Paracels shoals and even Hainan. To the east, it may at one time have included the Philippines and Celebes, but not the Moluccas. To the south it was limited by the deep sea beyond Java. It included all Sumatra and the Nicobar islands, and there is every reason to believe that it stretched out also to the west so as to include the central peak of Ceylon, the Maldive isles, and the Cocos islands west of Sumatra. We should then have an area as extensive as South America to 15° south latitude, and well calculated to develop that luxuriant fauna and flora which has since spread to the Himalayas. The submergence of the western half of this area (leaving only a fragment in Ceylon) would greatly diminish the number of animals and perhaps extinguish some peculiar types; but the remaining portion would still form a compact and extensive district, twice as large as the peninsula of India, over the whole of which a uniform Malayan fauna would prevail. The first important change would be the separation of Celebes; and this was probably effected by a great subsidence, forming the deep strait that now divides that island from Borneo. During the process Celebes itself was no doubt greatly submerged, leaving only a few islands in which were preserved that remnant of the ancient Malayan fauna that now constitutes one of its most striking and anomalous features. The Philippine area would next be separated, and perhaps be almost wholly submerged; or {360}broken up into many small volcanic islets in which a limited number of Malayan types alone survived. Such a condition of things will account for the very small variety of mammalia compared with the tolerably numerous genera of birds, that now characterise its fauna; while both here and in Celebes we find some of the old Malayan types preserved, which, in the extended area of the Sunda Isles have been replaced by more dominant forms. The next important change would be the separation of Java; and here also no doubt a considerable submergence occurred, rendering the island an unsuitable habitation for the various Malay types whose absence forms one of its conspicuous features. It has since remained permanently separated from the other islands, and has no doubt developed some peculiar species, while it may have preserved some ancient forms which in the larger area have become changed. From the fact that a number of its species are confined either to the western or the eastern half of the island, it is probable that it long continued as two islands, which have become united at a comparatively recent period. It has also been subjected to the immigration of Indo-Chinese forms, as already referred to in the earlier part of this sketch. We have thus shown how the main zoological features of the several sub-divisions of the Malayan sub-region may be accounted for, by means of a series of suppositions as to past changes which, though for the most part purely hypothetical, are always in accordance with what we know both of the physical geography and the zoology of the districts in question and those which surround them. It may also be remarked, that we know, with a degree of certainty which may be called absolute, that alternate elevation and subsidence is the normal state of things all over the globe; that it was the rule in the earliest geological epochs, and that it has continued down to the historical era. We know too, that the _amount_ of elevation and subsidence that can be proved to have occurred again and again in the same area, is often much greater than is required for the changes here speculated on,--while the _time_ required for such changes is certainly less than that necessitated by the changes {361}of specific and generic forms which have coincided with, and been to a large extent dependent on them. We have, therefore, true causes at work, and our only suppositions have been as to how those causes could have brought about the results which we see; and however complex and unlikely some of the supposed changes may seem to the reader, the geologist who has made a study of such changes, as recorded in the crust of the earth, will not only admit them to be probable, but will be inclined to believe that they have really been far more complex and more unexpected than any supposition we can make about them. There is one other external relation of the Malayan fauna about which it may be necessary to say a few words. I have supposed the greatest westward extension of the Malayan area to be indicated by the Maldive islands, but some naturalists would extend it to include Madagascar in order to account for the range of the Lemuridæ. Such an extension would, however, render it difficult to explain the very small amount of correspondence with a pervading diversity, between the Malayan and Malagasy faunas. It seems more reasonable to suppose an approximation of the two areas, without actual union having ever occurred. This approximation would have allowed the interchange of certain genera of birds, which are common to the Oriental Region and the Mascarene islands, but it would have been too recent to account for the diffusion of the lemurs, which belong to distinct genera and even distinct families. This probably dates back to a much earlier period, when the lemurine type had a wide range over the northern hemisphere. Subjected to the competition of higher forms, these imperfectly developed groups have mostly died out, except a few isolated examples, chiefly found in islands, and a few groups in Africa. In our discussion of the origin of the Ethiopian fauna, we have supposed that a close connection once existed between Madagascar and Ceylon. This was during a very early tertiary epoch; and if, long after it had ceased and the fauna of Ceylon and South India had assumed somewhat more of their present character, we suppose the approximation or union of Ceylon {362}and Malaya to have taken place, we shall perhaps be able to account for most of the special affinities they present, with the least amount of simultaneous elevation of the ocean bed; which it must always be remembered, requires a corresponding depression elsewhere to balance it. _Concluding Remarks on the Oriental Region._--We have already so fully discussed the internal and external relations of the several sub-regions, that little more need be said. The rich and varied fauna which inhabited Europe at the dawn of the tertiary period,--as shown by the abundant remains of mammalia wherever suitable deposits of Eocene age have been discovered,--proves, that an extensive Palæarctic continent then existed; and the character of the flora and fauna of the Eocene deposits is so completely tropical, that we may be sure there was then no barrier of climate between it and the Oriental region. At that early period the northern plains of Asia were probably under water, while the great Thibetan plateau and the Himalayan range, had not risen to more than a moderate height, and would have supported a luxuriant sub-tropical flora and fauna. The Upper Miocene deposits of northern and central India, and Burmah, agree in their mammalian remains with those of central and southern Europe, while closely allied forms of elephant, hyæna, tapir, rhinoceros, and _Chalicotherium_ have occurred in North China; leading us to conclude that one great fauna then extended over much of the Oriental and Palæarctic regions. Perim island at the mouth of the Red Sea, where similar remains are found, probably shows the southern boundary of this part of the old Palæarctic region in the Miocene period. Towards the equator there would, of course, be some peculiar groups; but we can hardly doubt, that, in that wonderful time when even the lands that stretched out furthest towards the pole, supported a luxuriant forest vegetation, substantially one fauna ranged over the whole of the great eastern continent of the northern hemisphere. During the Pliocene period, however, a progressive change went on which resulted in the complete differentiation of the Oriental and Palæarctic faunas. The {363}causes of this change were of two kinds. There was a great geographical and physical revolution effected by the elevation of the Himalayas and the Thibetan plateau, and, probably at the same time, the northward extension of the great Siberian plains. This alone would produce an enormous change of climate in all the extra-tropical part of Asia, and inevitably lead to a segregation of the old fauna into tropical and temperate, and a modification of the latter so as to enable it to support a climate far more severe than it had previously known. But it is almost certain that, concurrently with this, there was a change going on of a cosmical nature, leading to an alteration of the climate of the northern hemisphere from equable to extreme, and culminating in that period of excessive cold which drove the last remnants of the old sub-tropical fauna beyond the limits of the Palæarctic region. From that time, the Oriental and the Ethiopian regions alone contained the descendants of many of the most remarkable types which had previously flourished over all Europe and Asia; but the early history of these two regions, and the peculiar equatorial types developed in each, sufficiently separate them, as we have already shown. The Malayan sub-region is that in which characteristic Oriental types are now best developed, and where the fundamental contrast of the Oriental, as compared with the Ethiopian and Palæarctic regions, is most distinctly visible. {364}TABLES OF DISTRIBUTION. In constructing these tables, showing the distribution of various classes of animals in the Oriental region, the following sources of information have been chiefly relied on, in addition to the general treatises, monographs, catalogues, &c., used for the compilation of the Fourth Part of this work. _Mammalia._--Jerdon's Indian Mammalia; Kelaart's Fauna of Ceylon; Horsfield and Moore's Catalogue of the East India Museum; Swinhoe's Catalogue of Chinese Mammalia; S. Müller's Zoology of the Indian Archipelago; Dr. J. E. Gray's list of Mammalia of the Malay Archipelago (Voyage of Samarang); and papers by Anderson, Blyth, Cantor, Gray, Peters, Swinhoe, &c. _Birds._--Jerdon's Birds of India; Horsfield and Moore's Catalogue; Holdsworth's list of Ceylon Birds; Schlegel's Catalogue of the Leyden Museum; Swinhoe on the Birds of China, Formosa, and Hainan; Salvadori on the Birds of Borneo; Lord Walden on the Birds of the Philippine Islands; and papers by Blyth, Blanford, Elwes, Elliot, Stoliczka, Sclater, Sharpe, Swinhoe, Verreaux, and Lord Walden. _Reptiles._--Günther's Reptiles of British India; papers by same author, and by Dr. Stoliczka. {365}TABLE I. _FAMILIES OF ANIMALS INHABITING THE ORIENTAL REGION._ EXPLANATION. Names in _italics_ show families peculiar to the region. Numbers correspond with those in Part IV. Names enclosed thus (......) barely enter the region, and are not considered really to belong to it. ---------------------+-------------------+------------------------------- | Sub-regions | | 1=Hindostan. | Order and Family | 2=Ceylon. | Range beyond the Region. | 3=Indo-China. | | 4=Indo-Malaya. | ---------------------+----+----+----+----+------------------------------- | 1. | 2. | 3. | 4. | ---------------------+----+----+----+----+------------------------------- | | | | | MAMMALIA. | | | | | PRIMATES. | | | | | 1. Simiidæ | | | -- | -- |W. Africa 2. Semnopithecidæ | -- | -- | -- | -- |Tropical Africa 3. Cynopithecidæ | -- | -- | -- | -- |All Africa, S. Palæarctic 6. Lemuridæ | | -- | -- | -- |Ethiopian 7. _Tarsiidæ_ | | | | -- |Celebes | | | | | CHIROPTERA. | | | | | 9. Pteropidæ | -- | -- | -- | -- |Ethiopian, Australian 11. Rhinolophidæ | -- | -- | -- | -- |The Eastern Hemisphere 12. Vespertilionidæ | -- | -- | -- | -- |Cosmopolite 13. Noctilionidæ | -- | -- | -- | -- |Tropical regions | | | | | INSECTIVORA. | | | | | 14. _Galeopithecidæ_| | | | -- | 16. _Tupaiidæ_ | | -- | -- | -- | 17. Erinaceidæ | -- | -- | | -- |Palæarctic, S. Africa 21. Talpidæ | | | -- | |Palæarctic, Nearctic 22. Soricidæ | -- | -- | -- | -- |Palæarctic, Ethiopian, | | | | | N. America | | | | | CARNIVORA. | | | | | 23. Felidæ | -- | -- | -- | -- |All regions but Australian 25. Viverridæ | -- | -- | -- | -- |Ethiopian, S. Palæarctic 27. Hyænidæ | -- | | | |Ethiopian, S. Palæarctic 28. Canidæ | -- | -- | -- | -- |All regions but Australian [?] 29. Mustelidæ | -- | -- | -- | -- |All regions but Australian 31. Æluridæ | | | -- | |Palæarctic 32. Ursidæ | -- | -- | -- | -- |Palæarctic, Nearctic, Chili | | | | | CETACEA. | | | | |Oceanic | | | | | SIRENIA. | | | | | 42. Manatidæ | -- | -- | -- | -- |Ethiopian, N. Pacific | | | | | UNGULATA. | | | | | 43. (Equidæ) | -- | | | |Palæarctic, Ethiopian 44. Tapiridæ | | | | -- |Neotropical 45. Rinocerotidæ | | | -- | -- |Ethiopian 47. Suidæ | -- | -- | -- | -- |Palæarctic, Ethiopian, | | | | | Neotropical 49. Tragulidæ | -- | -- | -- | -- |W. Africa 50. Cervidæ | -- | -- | -- | -- |All regions but Ethiopian and | | | | | Australian 52. Bovidæ | -- | -- | -- | -- |All regions but Australian and | | | | | Neotropical 53. Elephantidæ | -- | -- | -- | -- |Ethiopian | | | | | RODENTIA. | | | | | 55. Muridæ | -- | -- | -- | -- |Cosmopolite, excl. Oceania 56. Spalacidæ | | | -- | -- |Palæarctic, Ethiopian 61. Sciuridæ | -- | -- | -- | -- |All regions but Australian 67. Hystricidæ | -- | -- | -- | -- |S. Palæarctic, Ethiopian 70. Leporidæ | -- | -- | -- | |All regions but Australian | | | | | EDENTATA. | | | | | 72. Manididæ | -- | -- | -- | -- |Ethiopian | | | | | BIRDS. | | | | | PASSERES. | | | | | 1. Turdidæ | -- | -- | -- | -- |Almost Cosmopolite 2. Sylviidæ | -- | -- | -- | -- |Almost Cosmopolite 3. Timaliidæ | -- | -- | -- | -- |Ethiopian, Australian 4. Panuridæ | | | -- | |Palæarctic 5. Cinclidæ | -- | -- | -- | -- |Not Ethiopian or Australian 6. Troglodytidæ | | | -- | -- |American and Palæarctic 8. Certhiidæ | -- | | -- | -- |Palæarctic, Nearctic, | | | | | Australian 9. Sittidæ | -- | -- | -- | -- |Palæarctic, Nearctic, | | | | | Australian, Madagascar 10. Paridæ | -- | -- | -- | -- |The Eastern Hemisphere and | | | | | North America 11. _Liotrichidæ_ | | | -- | -- | 12. _Phyllornithidæ_| -- | -- | -- | -- | 13. Pycnonotidæ | -- | -- | -- | -- |Ethiopian, Moluccas 14. Oriolidæ | -- | -- | -- | -- |The Eastern Hemisphere 15. Campephagidæ | -- | -- | -- | -- |Ethiopian, Australian 16. Dicruridæ | -- | -- | -- | -- |Ethiopian, Australian 17. Muscicapidæ | -- | -- | -- | -- |The Eastern Hemisphere 18. Pachycephalidæ | | | -- | -- |Australian 19. Laniidæ | -- | -- | -- | -- |The Eastern Hemisphere and | | | | | North America 20. Corvidæ | -- | -- | -- | -- |Cosmopolite 23. Nectariniidæ | -- | -- | -- | -- |Ethiopian, Australian 24. Dicæidæ | -- | -- | -- | -- |Ethiopian, Australian 30. Hirundinidæ | -- | -- | -- | -- |Cosmopolite 33. Fringillidæ | -- | -- | -- | -- |All regions but Australian 34. Ploceidæ | -- | -- | -- | -- |Ethiopian, Australian 35. Sturnidæ | -- | -- | -- | -- |The Eastern Hemisphere 36. Artamidæ | -- | -- | -- | -- |Australian 37. Alaudidæ | -- | -- | -- | -- |All regions but Neotropical 38. Motacillidæ | -- | -- | -- | -- |Cosmopolite 43. _Eurylæmidæ_ | | | -- | -- | 47. Pittidæ | -- | -- | -- | -- |Ethiopian, Australian | | | | | PICARIÆ. | | | | | 51. Picidæ | -- | -- | -- | -- |All regions but Australian 52. Yungidæ | -- | | | |Palæarctic 53. Indicatoridæ | | | -- | -- |Ethiopian 54. Megalæmidæ | -- | -- | -- | -- |Ethiopian, Neotropical 58. Cuculidæ | -- | -- | -- | -- |Cosmopolite 62. Coraciidæ | -- | -- | -- | -- |Ethiopian, Australian 63. Meropidæ | -- | -- | -- | -- |Ethiopian, Australian 66. Trogonidæ | -- | -- | -- | -- |Neotropical, Ethiopian 67. Alcedinidæ | -- | -- | -- | -- |Cosmopolite 68. Bucerotidæ | -- | -- | -- | -- |Ethiopian, Austro-Malayan 69. Upupidæ | -- | -- | -- | |Ethiopian, S. Palæarctic 71. Podargidæ | -- | -- | -- | -- |Australian 73. Caprimulgidæ | -- | -- | -- | -- |Cosmopolite 74. Cypselidæ | -- | -- | -- | -- |Cosmopolite | | | | | PSITTACI. | | | | | 76. (Cacatuidæ) | | | | -- |Australian 78. Palæornithidæ | -- | -- | -- | -- |Ethiopian, Austro-Malayan | | | | | COLUMBÆ. | | | | | 84. Columbidæ | -- | -- | -- | -- |Cosmopolite | | | | | GALLINÆ. | | | | | 86. Pteroclidæ | -- | | | |Ethiopian, Palæarctic 87. Tetraonidæ | -- | -- | -- | -- |Eastern Hemisphere and North | | | | | America 88. Phasianidæ | -- | -- | -- | -- |Ethiopian, Palæarctic, North | | | | | America 89. Turnicidæ | -- | -- | -- | -- |Ethiopian, Australian, | | | | | S. Palæarctic 90. Megapodiidæ | | | | -- |Australian | | | | | ACCIPITRES. | | | | | 94. Vulturidæ | -- | -- | -- | |All regions but Australian 96. Falconidæ | -- | -- | -- | -- |Cosmopolite 97. Pandionidæ | -- | -- | -- | -- |Cosmopolite 98. Strigidæ | -- | -- | -- | -- |Cosmopolite | | | | | GRALLÆ. | | | | | 99. Rallidæ | -- | -- | -- | -- |Cosmopolite 100. Scolopacidæ | -- | -- | -- | -- |Cosmopolite 103. Parridæ | -- | -- | -- | -- |Tropical regions 104. Glareolidæ | -- | -- | -- | -- |Eastern Hemisphere 105. Charadriidæ | -- | -- | -- | -- |Cosmopolite 106. Otididæ | -- | -- | -- | |Eastern Hemisphere 107. Gruidæ | -- | -- | -- | |All regions but Neotropical 113. Ardeidæ | -- | -- | -- | -- |Cosmopolite 114. Plataleidæ | -- | -- | -- | -- |Almost Cosmopolite 115. Ciconiidæ | -- | -- | -- | -- |Almost Cosmopolite 117. Phænicopteridæ | -- | -- | | |Ethiopian, Neotropical, | | | | | S. Palæarctic | | | | | ANSERES. | | | | | 118. Anatidæ | -- | -- | -- | -- |Cosmopolite 119. Laridæ | -- | -- | -- | -- |Cosmopolite 120. Procellariidæ | -- | -- | -- | -- |Cosmopolite 121. Pelecanidæ | -- | -- | -- | -- |Cosmopolite 124. Podicipidæ | -- | -- | -- | -- |Cosmopolite | | | | | REPTILIA. | | | | | OPHIDIA. | | | | | 1. Typhlopidæ | -- | -- | -- | -- |All regions but Nearctic 2. Tortricidæ | -- | -- | -- | -- |Austro-Malaya, S. America 3. _Xenopeltidæ_ | | | -- | -- |Celebes 4. _Uropeltidæ_ | | -- | | | 5. Calamariidæ | -- | -- | -- | -- |All the warmer regions 6. Oligodontidæ | -- | -- | -- | -- |S. America, Japan 7. Colubridæ | -- | -- | -- | -- |Almost Cosmopolite 8. Homalopsidæ | -- | -- | -- | -- |All the regions 9. Psammophidæ | -- | | -- | -- |Ethiopian, S. Palæarctic 11. Dendrophidæ | -- | -- | -- | -- |Ethiopian, Australian, | | | | | Neotropical 12. Dryiophidæ | -- | -- | -- | -- |Ethiopian, Neotropical 13. Dipsadidæ | -- | -- | -- | -- |Ethiopian, Australian, | | | | | Neotropical 14. Scytalidæ | | | | -- |Tropical America 15. Lycodontidæ | -- | -- | -- | -- |Ethiopian 16. Amblycephalidæ | | | -- | -- |Neotropical 17. Pythonidæ | -- | -- | -- | -- |The tropical regions, and | | | | | California 18. Erycidæ | -- | | -- | |Ethiopian, S. Palæarctic 19. _Acrochordidæ_ | | -- | | -- | 20. Elapidæ | -- | -- | -- | -- |Tropical regions, Japan, | | | | | S. Carolina 23. Hydrophidæ | -- | -- | -- | -- |Australian, Panama, Madagascar 24. Crotalidæ | -- | -- | -- | -- |America, E. Palæarctic 25. Viperidæ | -- | -- | -- | -- |Ethiopian, Palæarctic | | | | | LACERTILIA. | | | | | 30. Varanidæ | -- | -- | -- | -- |Africa, Australia 33. Lacertidæ | -- | -- | -- | -- |The Eastern Hemisphere 34. Zonuridæ | | | -- | |America, S. Europe, Ethiopian 45. Scincidæ | -- | -- | -- | -- |Almost Cosmopolite 48. Acontiadæ | | -- | | |Ethiopian, Moluccas 49. Geckotidæ | -- | -- | -- | -- |Almost Cosmopolite 51. Agamidæ | -- | -- | -- | -- |The Eastern Hemisphere 52. Chamæleonidæ | -- | -- | | |Ethiopian | | | | | CROCODILIA. | | | | | 54. Gavialidæ | -- | | | -- |N. Australia 55. Crocodilidæ | -- | -- | -- | -- |Ethiopian, Neotropical, | | | | | N. Australia | | | | | CHELONIA. | | | | | 57. Testudinidæ | -- | -- | -- | -- |All continents but Australia 59. Trionychidæ | -- | -- | -- | -- |Japan, E. of N. America, | | | | | Africa 60. Cheloniidæ | | | | |Marine | | | | | AMPHIBIA. | | | | | PSEUDOPHIDIA. | | | | | 1. Cæciliadæ | -- | -- | -- | |Ethiopian, Neotropical | | | | | URODELA. | | | | | 5. Salamandridæ | | | -- | |North temperate zone | | | | | ANOURA. | | | | | 7. Phryniscidæ | | | | -- |Ethiopian, Australian, | | | | | Neotropical 9. Bufonidæ | -- | -- | -- | -- |All continents but Australia 11. Engystomidæ | -- | -- | -- | -- |All regions but Palæarctic 16. Hylidæ | | | -- | |All regions but Ethiopian 17. Polypedatidæ | -- | -- | -- | -- |Neotropical and all other | | | | | regions 18. Ranidæ | -- | -- | -- | -- |Almost Cosmopolite 19. Discoglossidæ | | -- | -- | -- |All regions but Nearctic | | | | | FISHES. (FRESHWATER).| | | | | ACANTHOPTERYGII. | | | | | 3. Percidæ | -- | -- | -- | -- |All regions but Australian 12. Scienidæ | -- | -- | -- | -- |All regions but Australian 33. Nandidæ | -- | -- | -- | -- |Neotropical 35. Labyrinthici | -- | -- | -- | -- |S. Africa, Moluccas 36. _Luciocephalidæ_| | | | -- | 39. _Ophiocephalidæ_| -- | -- | -- | -- | 46. _Mastacembelidæ_| -- | -- | -- | -- | 52. Chromidæ | | -- | | |Ethiopian, Neotropical | | | | | PHYSOSTOMI. | | | | | 59. Siluridæ | -- | -- | -- | -- |All warm regions 73. Cyprinodontidæ | -- | -- | -- | -- |S. Palæarctic, Ethiopian, | | | | | American 75. Cyprinidæ | -- | -- | -- | -- |Not in S. America and Australia 78. Osteoglossidæ | | | | -- |All tropical regions 82. Notopteridæ | -- | -- | -- | -- |W. Africa 85. Symbranchidæ | -- | | -- | -- |Australian (? Marine) | | | | | Neotropical | | | | | INSECTS. | | | | | LEPIDOPTERA (PART). | | | | | DIURNI (BUTTERFLIES.)| | | | | 1. Danaidæ | -- | -- | -- | -- |All warm regions and to Canada 2. Satyridæ | -- | -- | -- | -- |Cosmopolite 3. Elymniidæ | | | -- | -- |Ethiopian, Moluccas 4. Morphidæ | | | -- | -- |Neotropical, Moluccas, and | | | | | Polynesia 6. Acræidæ | -- | -- | -- | -- |All tropical regions 8. Nymphalidæ | -- | -- | -- | -- |Cosmopolite 9. Libytheidæ | -- | -- | -- | -- |Absent from Australia 10. Nemeobeidæ | | | -- | -- |Not in Australia or Nearctic | | | | | regions 13. Lycænidæ | -- | -- | -- | -- |Cosmopolite 14. Pieridæ | -- | -- | -- | -- |Cosmopolite 15. Papilionidæ | -- | -- | -- | -- |Cosmopolite 16. Hesperidæ | -- | -- | -- | -- |Cosmopolite | | | | | SPHINGIDEA. | | | | | 17. Zygænidæ | -- | -- | -- | -- |Cosmopolite 19. Agaristidæ | -- | -- | -- | -- |Australian, Ethiopian 20. Uraniidæ | -- | -- | -- | -- |All tropical regions 22. Ægeriidæ | -- | -- | -- | -- |Absent from Australia 23. Sphingidæ | -- | -- | -- | -- |Cosmopolite ---------------------+----+----+----+----+------------------------------- TABLE II. GENERA OF TERRESTRIAL MAMMALIA AND BIRDS INHABITING THE ORIENTAL REGION. EXPLANATION. Names in _italics_ show genera peculiar to the region. Names inclosed thus (...) show genera which just enter the region, but are not considered properly to belong to it. Genera truly belonging to the region are numbered consecutively. _MAMMALIA._ -------------------+-------+----------------------+---------------------- Order, Family, and | No. of| Range within | Range beyond Genus. |Species| the Region. | the Region. -------------------+-------+----------------------+---------------------- | | | PRIMATES. | | | SIMIIDÆ. | | | | | | 1. _Simia_ | 2 |Borneo and Sumatra | 2. _Hylobates_ | 7 |Sylhet to Java and | | | S. China | 3. _Siamanga_ | 1 |Malacca and Sumatra | | | | SEMNOPITHECIDÆ. | | | | | | 4. _Presbytes_ | 28 |Simla to Aracan and |Moupin, Palæarctic [?] | | E. Thibet, Ceylon, | | | and Java | | | | CYNOPITHECIDÆ. | | | | | | 5. _Macacus_ | 22 |The whole region |S. Palæarctic 6. _Cynopithecus_ | 1 |Philippines |Celebes | | | (_Sub-Order_) | | | _LEMUROIDEA._ | | | | | | LEMURIDÆ. | | | | | | 7. _Nycticebus_ | 3 |E. Bengal to Java, and | | | S. China | 8. _Loris_ | 1 |Ceylon and S. India | | | | TARSIIDÆ. | | | | | | 9. _Tarsius_ | 1 |Sumatra, Borneo and | N. Celebes | | Philippines | | | | CHIROPTERA. | | | PTEROPIDÆ. | | | | | | 10. Pteropus | 6 |The whole region |Tropics of E. Hemisp. 11. Xantharpyia | 1 |The whole region |Austro-Malaya, | | | Ethiop., | | | S. Palæarctic 12. Cynopterus | 3 |The whole region |Tropical Africa 13. _Megærops_ | 1 |Sumatra | 14. Macroglossus | 1 |Java, Borneo, |Austro-Malaya | | Philippines | 15. Harpyia | 1 |Philippines |Austro-Malaya | | | RHINOLOPHIDÆ. | | | | | | 16. _Aquias_ | 2 |Nepal to Java | 17. _Phyllotis_ | 1 |Philippines | 18. Rhinolophus | 10 |The whole region |Warmer parts of | | | E. Hem. 19. Hipposideros | 8 |The whole region |Austro-Malaya 20. Phyllorhina | 4 |Indo-Malay subregion |Austro-Malaya, | | | Tropical Africa 21. Asellia | 1 |Java, Sumatra |Amboyna, Egypt 22. _Petalia_ | 1 |Java | 23. _Coelops_ | 1 |India (Bengal) | 24. _Rhinopoma_ | 1 |All India |Egypt, Palestine 25. Megaderma | 2 |The whole region |Ternate, N. Ethiopian 26. Nycteris | 1 |Java |Ethiopian | | | VESPERTILIONIDÆ. | | | | | | 27. Scotophilus | 10 |The whole region |Austral., Nearc., | | | Neotrop. 28. Vespertilio | 12 |The whole region |Cosmopolite 29. Keriovula | 8 |The whole region |S. Africa, N. China 30. _Trilatitus_ | 2 |Indo-Malaya |? 31. _Noctulina_ | 3 |Nepal to Philippines |? 32. Miniopteris | 3 |Java, Philippines, and |S. Africa, | | China | S. Palæarctic, | | | Australian 33. _Murina_ | 2 |Himalayas to Java |? 34. Nycticejus | 8 |All India |Trop. Africa, Temp. . | | | Amer 35. Harpiocephalus | 2 |Java and Philippines | 36. Taphozous | 4 |The whole region |Ethiop., Austro- | | | Malayan, Neotropical 37. _Myotis_ | 3 |Himalayas | 38. Plecotus | 1 |Darjeeling |Timor, S. Palæarctic 39. Barbastellus | 1 |Himalayas |Europe 40. Nyctophilus | 1 |Mussoorie |Australian | | | NOCTILIONIDÆ. | | | | | | 41. _Chiromeles_ | 1 |Indo-Malaya, Siam | 42. Nyctinomus | |The whole region |Madagascar, America | | | INSECTIVORA. | | | GALEOPITHECIDÆ. | | | | | | 43. _Galeopithecus_| 2 |Indo-Malay and | | | Philippines, excl. | | | Java | | | | TUPAIIDÆ. | | | | | | 44. _Tupaia_ | 7 |S. and E. of India to | | | Borneo | 45. _Hylomys_ | 2 |Tenasserim to Java and | | | Borneo | 46. _Ptilocerus_ | 1 |Borneo | | | | ERINACEIDÆ. | | | | | | 47. Erinaceus | 2 |Hindostan and Formosa |Palæarctic, S. Africa 48. _Gymnura_ | 1 |Malacca, Sumatra, | | | Borneo | | | | TALPIDÆ. | | | | | | 49. Talpa | 2 |Himalayas to Assam, & |Palæarctic | | Formosa | | | | SORICIDÆ. | | | | | | 50. Sorex | 21 |The whole region |All regions but | | | Austral. and | | | S. America | | | CARNIVORA. | | | FELIDÆ. | | | | | | 51. Felis | 20 |The whole region |All regions but | | | Austral. (Lynx | 1 |Central India) |Palæarctic, Ethiopian 52. Cynælurus | 1 |S. and W. India |S. Palæarctic, | | | Ethiopian | | | VIVERRIDÆ. | | | | | | 53. Viverra | 2 |The whole region |Ethiopian, Moluccas 54. _Viverricula_ | 2 |India to China and Java| 55. _Prionodon_ | 2 |Nepal to Borneo and | | | Java | 56. _Hemigalea_ | 2 |Malacca and Borneo | 57. _Arctitis_ | 1 |Nepal to Sumatra and | | | Java | 58. _Paradoxurus_ | 8 |The whole region |Ke Islands (? | | | introduced) 59. _Paguma_ | 3 |Nepal to Malaya and | | | China | 60. _Arctogale_ | 1 |Tenasserim and Malaya | 61. _Cynogale_ | 1 |Borneo | 62. Herpestes | 7 |The whole reg., excl. |S. Palæarctic, | | Philippines | Ethiopian 63. Calogale | 4 |India to Cambodjia |Ethiopian 64. _Calictis_ | 1 |Ceylon ? | 65. _Urva_ | |N. India | 66. _Tæniogale_ | 1 |Central India | 67. _Onychogale_ | 1 |Ceylon | | | | HYÆNIDÆ. | | | | | | 68. Hyæna | 1 |Hindostan, open country|S. Palæarctic, | | | Ethiopian | | | CANIDÆ. | | | | | | 69. Canis | 2 |All India |Almost Cosmopolite 70. _Cuon_ | 1 |India to Java | 71. Vulpes | 4 |All India |All Continents but S. | | |America and Australia (Nyctereutes | 1 |China) |Japan and Amoorland | | | MUSTELIDÆ. | | | | | | 72. Martes | 2 |India, Ceylon, Java, |Palæarctic, Nearctic | | and China | 73. Mustela | 3 |Himalayas to Bhotan and|Palæarc., Ethiop., | | China | Nearc. 74. _Gymnopus_ | 2 |Nepal to Borneo | 75. _Barangia_ | 1 |Sumatra | 76. Lutra | 5 |The whole region |Palæarctic 77. Aonyx | 2 |N. India, Malaya |W. and S. Africa 78. _Arctonyx_ | 1 |Nepal to Aracan | (Meles | 1 |S. China) |Palæarctic genus 79. Mydaus | 1 |Sumatra, Java | 80. Mellivora | 1 |Hindostan |Ethiopian 81. _Helictis_ | 4 |Nepal, Formosa, China &| | | Java | | | | ÆLURIDÆ. | | | | | | 82. Ælurus | 1 |E. Himalayas to |Palæarctic ? | | E. Thibet | | | | URSIDÆ. | | | | | | 83. Ursus | 2 |Himalayas to China |Palæarctic, Nearctic 84. _Helarctos_ | 1 |Indo-Malaya | 85. _Melursus_ | 1 |Ganges to Ceylon | | | | CETACEA. | | | DELPHINIDÆ. | | | | | | 86. _Platanista_ | 2 |Ganges to India | | | | SIRENIA. | | | MANATIDÆ. | | | | | | 87. Halicore | 1 |Coasts of W. India, |E. Africa, | | Ceylon, and | N. Australia | | Indo-Malaya | | | | UNGULATA. | | | TAPIRIDÆ. | | | | | | 88. Tapirus | 1 |Malay Pen., Sumatra, |Neotropical | | Borneo | | | | RHINOCEROTIDÆ. | | | | | | 89. Rhinoceros | 5 |Nepal to Bengal, Siam, |Ethiopian | | & Java | | | | SUIDÆ. | | | | | | 90. Sus | 6 |The whole region |Palæarc., Austro- | | | Malaya | | | TRAGULIDÆ. | | | | | | 91. _Tragulus_ | 5 |India and Ceylon to | | | Cambodja and Java | | | | CERVIDÆ. | | | | | | 92. Cervus | 15 |The whole region |Palæarc., Amer., | | | Moluc. 93. _Cervulus_ | 4 |The whole region | (Moschus | 1 |Himalayas above 8,000 |Central Asia, | | feet) | Palæarctic | | | BOVIDÆ. | | | | | | 94. _Bibos_ | 3 |India to Burmah, | | | Formosa, and Java | 95. Bubalus | 1 |N. and N. Central India|Ethiopian, | | | S. Palæarctic 96. _Portax_ | 1 |Peninsula of India | 97. Gazella | 1 |Deserts and plains of |Palæarctic deserts | | India | 98. _Antilope_ | 1 |Open country of India | 99. _Tetraceros_ | 2 |Hilly districts all | | | over India | 100. Nemorhedus | 3 |E. Himalayas and |N. China and Japan | | Sumatra | 101. Capra | 1 |Neilgherries |Palæarctic, Nearctic | | | PROBOSCIDEA. | | | ELEPHANTIDÆ. | | | | | | 102. Elephas | |India to Siam, Sumatra |Ethiopian | | & Borneo | | | | RODENTIA. | | | MURIDÆ. | | | | | | 103. Mus | 50 |The whole region |The E. Hemisphere 104. Acanthomys | 1 |India |Ethiopian, Australian 105. _Phlæomys_ | 1 |Philippines | 106._Platacanthomys_| 1 |S. W. India | 107. Meriones | 2 |India and Ceylon |Palæarctic, Ethiopian 108. _Spalacomys_ | 1 |India | 109. Arvicola | 2 |Himalayas |Palæarctic, Nearctic | | | SPALACIDÆ. | | | | | | 110. Rhizomys | 3 |Nepal to Canton, |Abyssinia | | Malacca and Sumatra | | | | SCIURIDÆ. | | | | | | 111. Sciurus | 50 |The whole region |Cosmop., excl. | | | Austral. region 112. Sciuropterus | 9 |India, and Ceylon to |N. and E. Palæarctic | | Java, Formosa | 113. _Pteromys_ | 9 |India & Ceylon to |Japan | | Borneo, Java, Formosa| (Arctomys | 2 |W. Himalayas above |Palæarctic and | | 8,000 ft.) | Nearctic | | | HYSTRICIDÆ. | | | | | | 114. Hystrix | 3 |India and Ceylon, to |S. Palæarctic, | | Malacca & S. China | Ethiopian 115. Atherura | 2 |India to Malaya |West Africa 116. _Acanthion_ | 2 |Nepal to Borneo and | | | Java | | | | LEPORIDÆ. | | | | | | 117. Lepus | 5 |India and Ceylon to |All regions but | | S. China and Formosa | Austral. | | | ENDENTATA. | | | MANIDIDÆ. | | | | | | 118. Manis | 2 |Nepal to Ceylon, |Ethiopian | | S. China and Java | | | | _BIRDS._ PASSERES. | | | TURDIDÆ. | | | | | | 1. _Brachypteryx_ | 8 |Himalayas, Ceylon and | | | Java | 2. Oreocincla | 8 |N. W. Himalayas to E. |Palæarctic, Australian | | Thibet Ceylon, Burmah,| | | Malaya, Formosa | 3. Turdus | 26 |The whole region |Almost Cosmopolite 4. Geocichla | 9 |India & Ceylon to Java,|Celebes, Lombock, to | | Formosa | N. Australia 5. Monticola | 3 |The whole region |Palæarctic, Ethiopian, | | |Moluccas 6. _Orocætes_ | 2 |N. W. Himalayas, and | | | India | 7. _Zoothera_ | 3 |W. Himalayas to Aracan,|Lombock, Timor ? | | Java | | | | SYLVIIDÆ. | | | | | | 8. {_Orthotomus_ | 13 |The whole region | 9. {_Prinia_ | 11 |The whole reg., excl. | { | | Philippines | 10. {Drymæca | 13 |The whole reg., excl. |Ethiopian { | | Philippines | 11. {Cisticola | 6 |The whole region |Ethiopian, Australian 12. {_Suya_ | 5 |Nepal to S. China and | { | | Formosa | 13. {_Megalurus_ | 3 |Central India, Java, | | | Philippines | | | | 14. {Acrocephalus | 9 |India to Ceylon, S. |Palæarc., Ethiop., { | | China, and Philippines| Austral. {(Dumeticola | 2 |Nepal and E. Thibet) |A Palæarctic genus | | | 15. {Locustella | 4 |Nepal, Hindostan, |Palæarctic { | | S. China | 16. {Horites | 2 |Himalayas, Formosa |High Himal., E. Thibet | | | 17. {Phylloscopus | 10 |All India and Ceylon, |Palæarctic, Ethiopian { | | to China, Philippines| {(Gerygone | 1 |Philippine Islands) |Australian genus {(Hypolais | 1 |All India, ? migrant) |Palæarctic genus 18. {Abrornis | 26 |The whole reg., excl. |Cashmere, E. Thibet { | | Philippines | 19. {Reguloides | 2 |Himalayas and Central |Palæarctic { | | India | {(Regulus | 1 |N. W. Himalayas and |Palæarctic and | | E. Thibet) | Nearctic {(Sylvia | 2 |India and Ceylon) |Palæarctic genus {(Curruca | 2 |India) |Palæarctic genus | | | {(Cyanecula | 1 |India) |Palæarctic genus 20. {Calliope | 2 |Himalayas and Central |Palæarctic { | | India, Philippine | { | | Islands | 21. {Ruticilla | 8 |Himalayas to China and |Palæarctic, Ethiopian { | | Formosa | 22. {_Chæmarrhornis_ 1 |Himalayas to Burmah | 23. {_Larvivora_ | 10 |W. Himalayas to Ceylon,| { | | Malacca and China | 24. {_Notodela_ | 3 |Himalayas to Pegu, | { | | Java, Formosa | 25. {_Tarsiger_ | 2 |Nepal and W. Himalayas | {(Grandala | 1 |Nepal and E. Thibet, |Palæarctic genus | | high) | 26. {Copsychus | 6 |The whole region |Madagascar 27. {_Kittacincla_ | 5 |The whole region | 28. {Thamnobia | 2 |N. W. India, Hindostan,|Ethiopian { | | and Ceylon | {(Dromolæa | 1 |N. W. India) |Ethiopian genus {(Saxicola | 2 |N. W. India) |Palæarctic and { | | | Ethiopian 29. {Oreicola ? | 1 |Burmah |Timor {(Cercomela | 1 |N. W. India, a desert |N. E. Africa, { | | genus) | S. W. Asia 30. {Pratincola | 5 |The whole region |Palæarctic, Ethiopian, | | |Celebes, and Timor (Accentor | 2 |Himalayas, in winter) |Palæarctic genus | | | TIMALIIDÆ. | | | | | | 31. Pomatorhinus | 20 |The whole region |Australian 32. Malacocercus | 14 |All India to Burmah, |Arabia, Nubia | | Philippines | 33. Chatarrhæa | 5 |India, Burmah, |Palestine, Abyssinia | | Philippines | 34. _Layardia_ | 3 |India and Ceylon | 35. _Acanthoptila_ | 1 |Nepal | 36. _Garrulax_ | 22 |The whole region | 37. _Janthocincla_ | 8 |Himalayas to E. Thibet,| | | Sumatra, Formosa | 38._Gampsorhynchus_| 1 |Nepal | 39. _Grammatoptila_| 1 |N. India | 40._Trochalopteron_| 22 |N. W. Himalayas, India,| | | China, Formosa | 41. _Actinodura_ | 3 |E. Himalayas, 3,000 to | | | 10,000 | 42. _Pellorneum_ | 3 |India, Ceylon, | | | Tenasserim | 43. _Dumetia_ | 2 |India and Ceylon | 44. _Timalia_ | 10 |Malacca to Java | 45. _Stachyris_ | 6 |N. W. Himalayas to | | | China, Formosa, | | | Sumatra | 46. _Pyctoris_ | 3 |India, Ceylon, and | | | Up. Burmah | 47. _Mixornis_ | 8 |Himalayas to Borneo and| | | Java | 48. _Malacopteron_ | 3 |Malacca to Java | 49. Alcippe | 16 |The whole region |New Guinea 50. _Macronus_ | 1 |Malacca to Java | 51. _Cacopitta_ | 5 |Java, Borneo, Sumatra | 52. Trichastoma | 9 |Nepal, Malacca to Java |Celebes 53. _Napothera_ | 5 |Malacca to Java | 54. Drymocataphus | 6 |Malacca to Java, Ceylon|Timor 55. _Turdinus_ | 4 |Tenasserim, Malacca | 56. _Trichixos_ | 1 |Malacca, Borneo | 57. _Sibia_ | 6 |N. W. Himalayas to | | | Tenasserim, Formosa | | | | PANURIDÆ. | | | | | | 58. _Paradoxornis_ | 3 |Nepal to Aracan and E. | | |Thibet, 3,000-6,000 ft.| 59. Suthora | 8 |Himalayas to E. Thibet,|N. W. China, E. Thibet | | China, Formosa | 60. _Chlenasicus_ | 1 |Sikhim | | | | CINCLIDÆ. | | | | | | 61. Cinclus | 2 |Himalayas, China, and |Palæarctic and | | Formosa | American 62. Eupetes | 2 |Malacca and Sumatra |New Guinea 63. _Enicurus_ | 9 |N. W. Himalayas (to | | | 11,000 ft.) to Java | | | and West China | 64. _Myiophonus_ | 6 |All India (to 9,000 ft.|Turkestan | | in N. W. Himalayas) | | | S. China, Formosa, | | | Java, Sumatra | | | | TROGLODYTIDÆ. | | | | | | 65. _Tesia_ | 2 |Eastern Himalayas | 66. _Pnoepyga_ | 6 |N. W. Himalayas to | | | E. Thibet, Java | 67. Troglodytes | 1 |Himalayas to E. Thibet |Palæarctic and | | | American 68. _Rimator_ | 2 |Darjeeling | | | | CERTHIIDÆ. | | | | | | 69. Certhia | 2 |Himalayas |Palæarctic and | | | Nearctic 70. _Salpornis_ | 1 |Central India | 71. _Rhabdornis_ | 1 |Philippine Islands | (Tichodroma | 1 |Himalayas in winter) |Palæarctic genus | | | SITTIDÆ. | | | | | | 72. Sitta | 5 |Himalayas to S. India, |Palæarctic and | | S. China | Nearctic 73. _Dendrophila_ | 2 |All India and Ceylon to| | | Pegu and Java | | | | PARIDÆ. | | | | | | 74. Parus | 16 |The whole region |Palæarctic and | | | Nearctic 75. _Melanochlora_ | 2 |Nepal to Malacca and | | | Sumatra | 76. _Psaltria_ | 1 |West Java | 77. _Ægithaliscus_ | 6 |W. Himalayas to China |Afghanistan 78. _Sylviparus_ | 1 |W. Himalayas to Central| | | India and E. Thibet | 79. _Cephalopyrus_ | 1 |N. W. Himalayas | | | | LIOTRICHIDÆ. | | | | | | 80. _Liothrix_ | 3 |Nepal to S. W. China | 81. _Siva_ | 3 |Himalayas:--3,000-7,000| | | ft. | 82. _Minla_ | 4 |Nepal to E. Thibet; | | | moderate heights | 83. Proparus | 6 |N. W. Himalayas to |Perhaps also | | E. Thibet; high | Palæarctic 84. _Allotrius_ | 7 |N. W. Himalayas to | | | Tenasserim, E. Thibet| | | and Java | 85. _Cutia_ | 2 |Nepal and Sikhim | 86. _Yuhina_ | 4 |Himalayas to E. Thibet,|Perhaps Palæarctic | | high | 87. _Ixulus_ | 4 |Darjeeling to | | | Tenasserim | 88. _Myzornis_ | 1 |Nepal and Sikhim | | | | PHYLLORNITHIDÆ. | | | | | | 89. _Phyllornis_ | 10 |The whole region; | | | excluding China and | | | Philippines | 90. _Iora_ | 5 |The whole reg., excl. | | | Philippines | 91. _Erpornis_ | 2 |Nepal and Hainan | | | | PYCNONOTIDÆ. | | | | | | 92. _Microscelis_ | 5 |Burmah, China, Malaya |Japan 93. Pycnonotus | 40 |The whole region |Ethiopian 94. _Hemixus_ | 2 |Himalayas and Hainan | 95. Hypsipetes | 15 |The whole region |Madagascar 96. Criniger | 11 |India, Ceylon, Malaya, |Africa, Moluccas | | Hainan | 97. _Setornis_ | 3 |Malacca, Sumatra, | | | Borneo | 98. _Iole_ | 4 |Aracan and Malaya | | | | ORIOLIDÆ. | | | | | | 99. Oriolus | 12 |The whole region |Palæarc. Ethiopian, | | | Celebes, Flores 100. _Analcipus_ | 3 |Himalayas, Malaya, | | | Formosa, Hainan | | | | CAMPEPHAGIDÆ. | | | | | | 101. _Pericrocotus_ | 22 |The whole region |Lombock; the Amoor, | | | migrant 102. Graucalus | 7 |India, Ceylon, Malaya, |Australian | | Philippines, Hainan | | | and Formosa | 103. Campephaga | 1 |Philippine Islands |Celebes to N. Guinea 104. _Volvocivora_ | 7 |The whole reg., excl. | | | Philippines | 105. Lalage | 2 |Malaya and Philippines |Celebes to Pacific Is. 106. _Cochoa_ | 3 |Himalayas and Java | | | | DICRURIDÆ. | | | | | | 107. Dicrurus | 17 |The whole region |Ethiop. and Australian 108. _Bhringa_ | 2 |Himalayas to Burmah and| | | Java | 109. _Chibia_ | 1 |India to China |Pekin in summer 110. _Chaptia_ | 3 |India to Borneo and | | | Formosa | 111. _Irena_ | 3 |S. India and Ceylon, | | | Assam to Malaya and | | | Philippines | | | | MUSCICAPIDÆ. | | | | | | 112. _Muscicapula_ | 6 |Cashmere to W. China, | | | S. India | 113. Erythrosterna | 7 |The whole region, |Palæarctic and | | excluding Philippines| Madagascar 114. Xanthpygia | 2 |Malacca to China |N. China and Japan 115. _Hemipus_ | 1 |India and Ceylon | 116. _Pycnophrys_ | 1 |Java | 117. Hemichelidon | 3 |N. India to Ceylon, and|Eastern Asia | | China; ? Philippines | 118. _Niltava_ | 3 |Himalayas to W. China | 119. Cyornis | 14 |The whole region |Celebes and Timor 120. Cyanoptila | 1 |Hainan to Japan |Japan and N. China 121. _Eumyias_ | 8 |The whole reg., excl. | | | Philippines | 122. _Siphia_ | 9 |N. W. India, Ceylon, | | | Formosa, E. Thibet | 123. _Anthipes_ | 1 |Nepal | 124. _Schwaneria_ | 1 |Borneo | 125. _Hypothymis_ | 1 |The whole region |Celebes 126. Rhipidura | 7 |All India and Ceylon, | | | Malaya, Philippines |Australian 127. _Chelidorhynx_ | 1 |N. India | 128. _Cryptolopha_ | 1 |The whole region |Celebes | | | 129. Tchitrea | 6 |The whole region |N. China, and Japan, | | |Flores, Ethiopian 130. _Philentoma_ | 4 |Malaya and Philippines | | | | PACHYCEPHALIDÆ. | | | | | | 131. Hylocharis | 2 |Aracan to Malaya & |Celebes, Timor | | Philippines | | | | LANIIDÆ. | | | | | | 132. Lanius | 16 |The whole region |Nearc., Palæarc., | | | Ethiop. 133. _Laniellus_ | 1 |Java | 134. _Tephrodornis_ | 5 |India, Ceylon, and | | | Malaya; Hainan | | | | CORVIDÆ. | | | | | | 135. _Pityriasis_ | 1 |Borneo, Sumatra | 136. _Platylophus_ | 4 |Malaya | 137. Garrulus | 4 |Himalayas, S. China, |Palæarctic | | Formosa | 138. _Cissa_ | 3 |Himalayas and Aracan to| | | Java | 139. _Urocissa_ | 7 |N.W. Himalayas, Ceylon,|N. China and Japan | | Burmah, China, Formosa| 140. _Temnurus_ | 3 |Malaya and Cochin China| 141. _Dendrocitta_ | 8 |All India to S. China, | | | Formosa, and Sumatra | 142. _Crypsirhina_ | 2 |Java and Burmah | 143. Nucifraga | 2 |Himalayas and E. Thibet|Palæarctic genus | | 8,000-10,000 feet | 144. Pica | 2 |China and Himalayas of |Palæarctic and | | Boetan | Nearctic 145. Corvus | 9 |The whole region |Cosmop., excl. S. Am. (Fregilus | 2 |Himalayas, high) |Palæarctic genus | | | NECTARINIIDÆ. | | | | | | 146. _Æthopaga_ | 13 |Himalayas to W. China &|Celebes | | Java, Central India | 147. Chalcostetha | 1 |Malaya and Siam |Celebes to New Guinea 148. Arachnothera | 12 |The whole reg., excl. |Celebes, Lombock, New | | Philippine |Guinea 149. Arachnecthera | 7 |The whole region, excl.|Celebes to New Ireland | | China | 150. _Nectarophila_ | 4 |India, Ceylon, Malaya, |Celebes | | Philipp. | 151. _Anthreptes_ | 1 |Malaya and Indo-China |Celebes | | | DICÆIDÆ. | | | | | | 152. Dicæum | 10 |The whole region |Australian 153. Pachyglossa | 1 |Nepal |Celebes 154. _Piprisoma_ | 1 |India and Ceylon | 155. _Prionochilus_ | 4 |Malaya | 156. Zosterops | 8 |The whole region |Ethiopian, Australian 157. _Chalcoparia_ | 1 |Aracan to Malaya | | | | HIRUNDINIDÆ. | | | | | | 158. Hirundo | 10 |The whole region |Cosmopolite 159. Cotyle | 5 |India to China |Palæarc., Ethiop., | | | Amer. 160. Chelidon | 3 |India, Borneo |Palæarctic | | | FRINGILLIDÆ. | | | | | | (Fringilla | 1 |Himalayas, in winter) |Palæarctic genus (Acanthis | 1 |N. W. Himalayas, in |Palæarctic genus | | winter) | (Procarduelis | 1 |High Himalayas) |Palæarctic genus (Chlorospiza | 1 |China) |Palæarctic and | | | Ethiopian 161. Passer | 6 |The whole region |Palæarctic and | | | Ethiopian (Fringillauda | 1 |High Himalayas) |Palæarctic genus (Coccothraustes| 2 |High Himalayas) |Palæarctic and | | | Nearctic (Mycerobas | 1 |High Himalayas) |Palæarctic genus 162. Eophona | 1 |China |Palæarctic (Pyrrhula | 4 |Himalayas, winter) |Palæarctic (Carpodacus | 4 |Himalayas and Central |Palæarctic and | | India, in winter) | Nearctic (Loxia | 1 |Snowy Himalayas) |Palæarctic and | | | Nearctic (Propyrrhula | 1 |Darjeeling, in winter) |[?] Palæarctic 163. _Hæmatospiza_ | 1 |S. E. Himal., 5,000 to | | | 10,000 ft. | | | | (_S. Fam._ EMBERIZINÆ) | | | | | 164. Euspiza | 4 |N. W. India to Burmah, |Palæarctic and | | & China | Nearctic 165. Emberiza | 7 |All India and China, in|Palæarctic genus | | winter | | | | PLOCEIDÆ. | | | | | | 166. Ploceus | 4 |India & Ceylon, Burmah,|Ethiopian | | Malaya | 167. Munia | 20 |The whole region |Austro-Malayan 168. Estrilda | 2 |India and Ceylon, |Ethiopian, Australian | | Burmah, Java | 169. Erythrura | 1 |Java, Sumatra |Moluccas to Fiji | | | Islands | | | STURNIDÆ. | | | | | | 170. Eulabes | 7 |The whole reg., excl. |Flores, Papua | | Philippines | 171. _Ampeliceps_ | 1 |Tenasserim to | | | Cochin-China | 172. _Gymnops_ | 1 |Philippine Islands | 173. Pastor | 1 |All India to Burmah |S. Palæarctic 174. _Acridotheres_ | 6 |The whole region |Celebes 175. _Sturnia_ | 12 |The whole region |N. China & Japan, | | | Celebes 176. Sturnus | 3 |India and China |Palæarctic 177. _Sturnopastor_ | 3 |Cen. India to Burmah & | | | Malaya | 178. Calornis | 2 |Malaya and Philippines |[?] Celebes, Moluccas | | | to Samoan Islands 179. _Saroglossa_ | 1 |W. and Central | | | Himalayas | | | | ARTAMIDÆ. | | | | | | 180. Artamus | 3 |The whole region |Australian | | | ALAUDIDÆ. | | | | | | (Otocorys | 1 |N. India, in winter) |Palæarctic and | | | Nearctic 181. Alauda | 7 |India and China |Palæarctic and | | | Ethiopian 182. Galerita | 2 |Central India |Palæarctic 183. Calandrella | 2 |India and Burmah |Palæarctic and | | | Ethiopian (Melanocorypha | 1 |N. W. India) |Palæarctic 184. Mirafra | 5 |India, Ceylon, and Java|Ethiopian 185. Ammomanes | 1 |Central India |Palæarctic and | | | Ethiopian 186. Pyrrhulauda | 1 |India and Ceylon |Ethiopian | | | MOTACILLIDÆ. | | | | | | 187. Motacilla | 6 |India and Ceylon to |Palæarctic and | | China and Philippines| Ethiopian 188. Budytes | 2 |China and Philippines |Palæarctic & | | | Ethiopian, Moluccas 189. Calobates | 1 |The whole region |Palæarctic 190. _Nemoricola_ | 1 |India, Ceylon, and | | | Malaya | 191. Authus | 3 |India and China |Cosmopolite 192. Corydalla | 8 |The whole region |Palæarctic, Australian 193. _Heterura_ | 1 |Himalayas | | | | EURYLÆMIDÆ. | | | | | | 194. _Eurylæmus_ | 2 |Malaya | 195. _Serilophus_ | 1 |Himalayas | 196. _Psarisomus_ | 1 |Himalayas | 197. _Corydon_ | 1 |Malacca, Sumatra, | | | Borneo | 198. _Cymbirhynchus_| 2 |Aracan, Siam, and | | | Malaya | 199. _Calyptomena_ | 1 |Malacca, Sumatra, | | | Borneo | | | | PITTIDÆ | | | | | | 200. Pitta | 11 |The whole region |Australian, Ethiopian 201. _Eucichla_ | 3 |Malaya | 202. _Hydrornis_ | 3 |Himalayas and Malaya | | | | PICARIÆ. | | | PICIDÆ. | | | | | | 203. _Vivia_ | 1 |N. W. Himalayas to E. | | |Thibet, 3,000-6,000 ft.| 204. _Sasia_ | 2 |Nepal to Malaya and | | | Borneo | 205. Picus | 14 |The whole region, excl.|Palæarctic, American | | Philippines | 206. Hyopicus | 1 |Himalayas |N. China 207. _Yungipicus_ | 12 |The whole region |N. China, Japan, | | | Celebes 208._Reinwardtipicus_ 1 |Penang to Sumatra and | | | Borneo | 209. _Venilia_ | 2 |Nepal to Sumatra and | | | Borneo | 210._Chrysocolaptes_| 8 |India, Ceylon, Malaya, | | | Philippines | 211. _Hemicercus_ | 5 |Malabar, Pegu to Malaya| 212. Gecinus | 12 |All India and Ceylon to|Palæarctic | | Pegu and Malaya | 213. _Mulleripicus_ | 5 |Malabar, Aracan to |Celebes | | Malaya and Philippines| 214. _Brachypternus_| 5 |India, Ceylon, and | | | China | 215. _Tiga_ | 5 |India to Malaya | 216. _Gecinulus_ | 2 |S. Himalayas to Burmah | 217. _Miglyptes_ | 3 |Malaya | 218. _Micropternus_ | 8 |India and Ceylon, to | | | Borneo and S. China | | | | YUNGIDÆ. | | | | | | 219. Yunx | 1 |Central and S. China |Palæarctic, S. Africa | | | INDICATORIDÆ. | | | | | | 220. Indicator | 2 |Himalayas and Borneo |Ethiopian | | | MEGALÆMIDÆ. | | | | | | 221. _Megalæma_ | 27 |The whole region, excl.| | | Philippines | 222. _Xantholæma_ | 4 |All India and Ceylon to| | | Pegu and Malaya | 223. _Psilopogon_ | 1 |Sumatra | 224. _Caloramphus_ | 2 |Malacca, Sumatra and | | | Borneo | | | | CUCULIDÆ. | | | | | | 225. _Phoenicophaës_| 1 |Ceylon | 226. _Rhinococcyx_ | 1 |Java | 227. _Dasylophus_ | 1 |Philippine Islands | 228. _Lepidogrammus_| 1 |Philippine Islands | 229. _Carpococcyx_ | 1 |Borneo, Sumatra | 230. _Zanclostomus_ | 1 |Malaya | 231. _Rhopodytes_ | 7 |Nepal to Ceylon, Hainan| | | and Malaya | 232. _Taccocoua_ | 4 |All India, Ceylon, | | | Malacca | 233. _Poliococcyx_ | 1 |Malacca, Sumatra, | | | Borneo | 234. _Rhinortha_ | 1 |Malacca, Sumatra, | | | Borneo | 235. Centropus | 14 |The whole region |Ethiopian, Australian 236. Cuculus | 10 |The whole region |Palæarc., Ethiop., | | | Aust. 237. Cacomantis | 9 |The whole region |Australian 238. Chrysococcyx | 5 |The whole region |Ethiopian, Australian 239. _Surniculus_ | 2 |India, Ceylon and | | | Malaya | 240. Hierococcyx | 6 |The whole region |Celebes, N. China and | | | Amoorland 241. Coccystes | 2 |The whole region, excl.|Ethiopian | | Philippines | 242. Eudynamis | 2 |The whole region |Australian | | | CORACIIDÆ. | | | | | | 243. Coracias | 2 |India, Ceylon and |Ethiopian, S. | | Burmah | Palæarctic, Celebes 244. Eurystomus | 1 |The whole region |Ethiopian, Australian | | | MEROPIDÆ. | | | | | | 245. _Nyctiornis_ | 3 |S. India to Himalayas, | | | Burmah, Sumatra, and | | | Borneo | 246. Merops | 5 |The whole region |S. Palæarctic, | | | Ethiopian, | | | Australian | | | TROGONIDÆ. | | | | | | 247. _Harpactes_ | 10 |The whole region, excl.| | | China | | | | ALCEDINIDÆ. | | | | | | 248. Halcyon | 10 |The whole region |S. Palæarctic, | | | Ethiopian, | | | Australian 249. _Pelargopsis_ | 7 |The whole region, excl.|Celebes and Timor | | China | 250. _Carcineutes_ | 2 |Burmah, Siam, and | | | Malaya | 251. Ceyx | 6 |India and Ceylon, |Moluccas & New Guin. | | Malaya and Philippines| 252. Alcedo | 5 |The whole region |Palæarctic, Ethiopian, | | |Austro-Malayan 253. Alcyone | 1 |Philippines |Australian genus 254. Ceryle | 2 |India to S. China |Ethiopian, S. | | | Palæarctic, American | | | BUCEROTIDÆ. | | | | | | 255. _Buceros_ | 4 |Nepal to Malaya, S. | | | India, Philippines | 256. _Hydrocissa_ | 7 |India, Ceylon and | | | Malaya | 257. Berenicornis | 1 |Sumatra |W. Africa 258. Calao | 2 |Tenasserim, Malaya |Austro-Malaya 259. _Aceros_ | 1 |S. E. Himalayas | 260. _Cranorrhinus_ | 2 |Malacca to Borneo and |Celebes | | Philippines | 261. _Penelopides_ | 1 |Philippines | 262. _Rhinoplax_ | 1 |Sumatra, Borneo | 263. _Meniceros_ | 3 |India and Ceylon to | | | Tenasserim | | | | UPUPIDÆ. | | | | | | 264. Upupa | 3 |India, Ceylon and |Ethiopian, | | Burmah | S. Palæarctic | | | PODARGIDÆ. | | | | | | 265. Batrachostomus | 6 |India, Ceylon and |Moluccas | | Malaya | | | | CAPRIMULGIDÆ. | | | | | | 266. Caprimulgus | 13 |The whole region |The Eastern | | | Hemisphere 267. _Lyncornis_ | 4 |Burmah, Malaya, & |Celebes | | Philippines | | | | CYPSELIDÆ. | | | | | | 268. Cypselus | 8 |The region, excl. |The Old World & | | Philippines | S. Amer. 269. Dendrochelidon | 3 |Ceylon, India, Malaya, |Austro-Malaya | | Philipp. | 270. Collocalia | 3 |The whole region |Madagascar, Moluccas, | | | Pacific Islands 271. Chætura | 3 |Ceylon, India, Malaya, |America, Africa | | Hainan | | | | PSITTACI. | | | CACATUIDÆ. | | | | | | (Cacatua | 1 |Philippines) |Australian genus | | | PALÆORNITHIDÆ. | | | | | | 272. Palæornis | 14 |N. W. India to Ceylon, |Ethiopian | | Siam & Malaya | 273. Prioniturus | 1 |Philippine Islands |Celebes 274. Cyclopsitta | 1 |Philippine Islands |Papuan Islands 275. _Psittinus_ | 1 |Malaya, excl. Java | 276. Tanygnathus | 1 |Philippine Islands |Austro-Malaya 277. Loriculus | 9 |Ceylon, India, Malaya, |Celebes and Moluccas, | | Philippines | Flores | | | COLUMBÆ. | | | COLUMBIDÆ. | | | | | | 278. Treron | 21 |The whole region |Ethiopian, Moluccas 279. Ptilopus | 3 |Malaya and Philippines |Australian 280. Carpophaga | 10 |India and Ceylon to |Australian | | Hainan and Philippines| 281. Columba | 7 |Ceylon and India to |Palæarc., Ethiop., | | Tenasserim | Amer. 282. Janthænas | 3 |Philippine, Andaman & |Japan, Moluccas to | | Nicobar Islands | Samoan Islands 283. Macropygia | 6 |Nepal, Java, Hainan, |Austro-Malaya, | | Philippines | Australia 284. Turtur | 8 |The whole region |Old World, Austro- | | | Malay. 285. Chalcophaps | 2 |India, Ceylon, Malaya, |Austro-Malaya, | | Hainan, Philippines, | Australia | | Formosa | 286. _Phapitreron_ | 2 |Philippine Islands | 287. Caloenas | 1 |Nicobar and Philippine |Austro-Malaya | | Islands | 288. Phlegoenas | 2 |Philippine and Sooloo |Austro-Mal. & | | Islands | Polynesia 289. Geopelia | 1 |Philippine Islands, |Austro-Malaya & | | Java | Austral. | | | GALLINÆ. | | | PTEROCLIDÆ. | | | | | | 290. Pterocles | 2 |Central and S. India |S. Palæarctic, | | | Ethiopian | | | TETRAONIDÆ. | | | | | | 291. Francolinus | 3 |Ceylon and India to |S. Palæarctic, | | S. China | Ethiopian 292. _Ortygornis_ | 3 |Ceylon to Himalayas, | | | Sumatra & Borneo | 293. Perdix | 12 |India, Malaya, |Palæarctic | | Philippines, China | 294. Coturnix | 9 |The whole region |The Eastern Hemisphere 295. _Rollulus_ | 2 |Malacca, Siam, Borneo, | | | Philipp. | (Caccabis | 1 |W. Himalayas) |Palæarctic genus | | | PHASIANIDÆ. | | | | | | 296. _Pavo_ | 2 |Ceylon to Himalayas, | | | S. W. China and Java | | | | 297. _Argusianus_ | 4 |Siam, Malacca, Borneo | 298. _Polyplectron_ | 5 |Upper Assam to S. W. | | | China & Sumatra | (Lophophorus | 3 |Cashmere and E. Thibet)|Palæarctic genus (Tetraophasis | 1 |E. Thibet) |Palæarctic genus 299. Ceriornis | 5 |N. W. Himalayas to |S. E. Palæarctic | | W. China | (Pucrasia | 3 |N. W. Himalayas to N. |Palæarctic genus | | China and Mongolia) | 300. Phasianus | 3 |W. Himalayas, S. China,|S. Palæarctic | | Formosa | 301. _Euplocamus_ | 13 |N. W. Himalayas to | | | China, Sumatra and | | | Borneo | 302. _Gallus_ | 4 |The region, excl. China|Celebes and Timor 303. _Galloperdix_ | 3 |Central India to Ceylon| | | | TURNICIDÆ. | | | | | | 304. Turnix | 9 |The whole region |S. Palæarc., | | | Ethiopian, Australian | | | MEGAPODIIDÆ. | | | | | | 305. Megapodius | 2 |Nicobar Is., |Celebes to Samoan Is., | | Philippines, N. W. | N. Australia | | Borneo | | | | ACCIPITRES. | | | VULTURIDÆ. | | | | | | 306. Vultur | 1 |Himalayas |S. Palæarctic, | | | Ethiopian 307. Gyps | 3 |India and Siam |S. Palæarctic, | | | Ethiopian 308. _Pseudogyps_ | 1 |India and Burmah |N. Ethiopian 309. Neophron | 1 |All India |S. Palæarctic, | | | Ethiopian | | | FALCONIDÆ. | | | | | | 310. Circus | 4 |India and China |Almost Cosmopolite 311. Astur | 4 |The whole region |Almost Cosmopolite 312. Accipiter | 2 |The whole region |Almost Cosmopolite 313. Buteo | 2 |India to China |Cosmopolite; excl. | | | Austl. 314. Aquila | 4 |India to China |Nearc, Palæarc., | | | Ethiop. 315. Nisaëtus | 2 |India and Ceylon |S. Palæar., Ethiop., | | | Aus. 316. Lophotriorchis | 1 |Indo-Malaya |Neotropical 317. Neopus | 1 |India to Burmah and |Celebes and Moluccas | | Malaya | 318. Spizaëtus | 5 |India to Malaya and |Neotropical, | | Formosa | Ethiopian, | | | Austro-Malayan 319. Circaëtus | 1 |Indian peninsula |Palæarc., Ethiop., | | | Timor 320. _Spilornis_ | 5 |The whole region |Celebes 321. Butastur | 3 |The whole region |N. E. Africa, Celebes, | | |New Guinea 322. Haliæetus | 2 |The whole region |Cosmopolite; excl. | | | Neotropical region 323. Haliastur | 1 |India to Malaya |Austro-Malaya, | | | Austral. 324. Milvus | 3 |The whole region |The Eastern | | | Hemisphere. 325. Elanus | 2 |India, Malaya |Africa, Australia 326. Machærhamphus | 1 |Malacca |S. W. Africa & Madag. 327. Pernis | 1 |India |Palæarctic and | | | Ethiopian, Celebes 328. Baza | 3 |India to Malaya | | |Moluccas and N. Austrl.| 329. _Hierax_ | 4 |N. India, Burmah, | | | Malaya | 330. Poliohierax | 1 |Burmah |E. Africa 331. Falco | 8 |The whole region |Almost Cosmopolite 332. Cerchneis | 3 |The whole region |Almost Cosmopolite | | | PANDIONIDÆ. | | | | | | 333. Pandion | 1 |The whole region |Cosmopolite 334. Polioaëtus | 2 |India to Malaya |Indo-Malaya & | | | Polynesia | | | STRIGIDÆ. | | | | | | 335. Athene | 9 |The whole region |The Eastern Hemisphere 336. _Ninox_ | 7 |The whole region |N. China and Japan 337. Bubo | 4 |India, Ceylon, Malaya |Cosmop. exc. Austr. | | and Philip. | reg. 338. _Ketupa_ | 3 |The whole region | 339. Scops | 7 |The whole region |Almost Cosmopolite 340. Syrnium | 6 |The whole region |Cosmop. exc. Austr. | | | reg. (Asio | 2 |India) |Palæarc., Ethiop. | | | Amer. 341. Strix | 4 |The whole region |Cosmopolite 342. _Phodilus_ | 2 |Nepal, Malaya | _Peculiar or very Characteristic Genera of Wading or Swimming Birds._ | | | GRALLÆ. | | | RALLIDÆ. | | | | | | Rallina | 10 |The whole region |Austro-Malaya | | | PARRIDÆ. | | | | | | _Hydrophasanus _| 1 |The whole region | | | | CHARADRIIDÆ. | | | | | | Æsacus | 1 |The whole region |Austro-Malayan, Austra [Illustration: AUSTRALIAN REGION] {387}CHAPTER XIII. THE AUSTRALIAN REGION. The Australian is the great insular region of the earth. As a whole it is one of the best marked, and has even been considered to be equal in zoological value to all the rest of the globe; but its separate portions are very heterogeneous, and their limits sometimes ill-defined. Its central and most important masses consist of Australia and New Guinea, in which the main features of the region are fully developed. To the north-west it extends to Celebes, in which a large proportion of the Australian characters have disappeared, while Oriental types are mingled with them to such an extent that it is rather difficult to determine where to locate it. To the south-east it includes New Zealand, which is in some respects so peculiar, that it has even been proposed to constitute it a distinct region. On the east it embraces the whole of Oceania to the Marquesas and Sandwich Islands, whose very scanty and often peculiar fauna, must be affiliated to the general Australian type. Australia is the largest tract of land in the region, being several times more extensive than all the other islands combined, and it is here that the greatest variety of peculiar types have been developed. This island-continent, being situated in the track of the southern desert zone, and having no central mountains to condense the vapours from the surrounding ocean, has a large portion of its interior so parched up and barren as to be almost destitute of animal life. The most extensive tract of fertile and well-watered country is on the east and south-east, {388}where a fine range of mountains reaches, in the Colony of Victoria, the limits of perpetual snow. The west coast also possesses mountains of moderate height, but the climate is very dry and hot. The northern portion is entirely tropical, yet it nowhere presents the luxuriance of vegetation characteristic of the great island of New Guinea immediately to the north of it. Taken as a whole, Australia is characterized by an arid climate and a deficiency of water; conditions which have probably long prevailed, and under which its very peculiar fauna and flora have been developed. This fact will account for some of the marked differences between it and the adjacent sub-regions of New Guinea and the Moluccas, where the climate is moist, and the vegetation luxuriant; and these divergent features must never be lost sight of, in comparing the different portions of the Australian region. In Tasmania alone, which is however, essentially a detached portion of Australia, a more uniform and moister climate prevails; but it is too small a tract of land, and has been too recently severed from its parent mass to have developed a special fauna. The Austro-Malay sub-region (of which New Guinea is the central and typical mass) is strikingly contrasted with Australia, being subjected to purely equatorial conditions,--a high, but uniform temperature, excessive moisture, and a luxuriant forest vegetation, exactly similar in general features to that which clothes the Indo-Malay Islands, and the other portions of the great equatorial forest zone. Such a climate and vegetation, being the necessary result of its geographical position, must have existed from remote geological epochs with but little change, and must therefore have profoundly affected all the forms of life which have been developed under their influence. Around New Guinea as a centre are grouped a number of important islands, more or less closely agreeing with it in physical features, climate, vegetation, and forms of life. In most immediate connection we place the Aru Islands, Mysol and Waigiou, with Jobie and the other Islands in Geelvinck Bay, all of which are connected with it by shallow seas; they possess one of its most characteristic groups, the Birds of Paradise, and have no doubt only recently (in {389}a geological sense) been separated from it. In the next rank come the large islands of the Moluccas on the west, and the range terminating in the Solomon Islands on the east, both of which groups possess a clearly Papuan fauna, although deficient in many of the most remarkable Papuan types. All these islands agree closely with New Guinea itself in being very mountainous, and covered with a luxuriant forest vegetation; but to the south-west we find a set of islands extending from Timor to Lombock, which agree more nearly with Australia, both in climate and vegetation; being arid and abounding in eucalypti, acacias, and thickets of thorny shrubs. These, like the Moluccas, are surrounded by deep sea, and it is doubtful whether they have either of them been actually connected with New Guinea or Australia in recent geological times; but the general features of their zoology oblige us to unite all these islands with New Guinea as forming the Austro-Malay sub-division of the Australian region. Still further west however, we have the large island of Celebes, whose position is very difficult to determine. It is mountainous, but has also extensive plains and low lands. Its climate is somewhat arid in the south, where the woods are often scattered and thorny, while in the north it is moister, and the forests are luxuriant. It is surrounded by deep seas, but also by coralline and volcanic islets, indicating former elevations and subsidences. Its fauna presents the most puzzling relations, showing affinities to Java, to the Philippines, to the Moluccas, to New Guinea, to continental India, and even to Africa; so that it is almost impossible to decide whether to place it in the Oriental or the Australian region. On the whole the preponderance of its relations appears to be with the latter, though it is undoubtedly very anomalous, and may, with almost as much propriety, be classed with the former. This will be better understood when we come to discuss its zoological peculiarities. The next sub-region consists of the extensive series of islands scattered over the Pacific, the principal groups being the Sandwich Islands, the Marquesas and Society Islands, the Navigators', Friendly, and Fiji Islands. New Caledonia and the New {390}Hebrides have rather an uncertain position, and it is difficult to decide whether to class them with the Austro-Malay Islands, the Pacific Islands, or Australia. The islands of the west Pacific, north of the equator, also probably come into this region, although the Ladrone Islands may belong to the Philippines; but as the fauna of all these small islets is very scanty, and very little known, they are not at present of much importance. There remains the islands of New Zealand, with the surrounding small islands, as far as the Auckland, Chatham, and Norfolk Islands. These are situated in the south temperate forest-zone. They are mountainous, and have a moist, equable, and temperate climate. They are true oceanic islands, and the total absence of mammalia intimates that they have not been connected with Australia or any other continent in recent geological times. The general character of their zoology, no less than their botany, affiliates them however, to Australia as portions of the same zoological region. _General Zoological Characteristics of the Australian Region._--For the purpose of giving an idea of the very peculiar and striking features which characterise the Australian region, it will be as well at first to confine ourselves to the great central land masses of Australia and New Guinea, where those features are manifested in their greatest force and purity, leaving the various peculiarities and anomalies of the outlying islands to be dealt with subsequently. _Mammalia._--The Australian region is broadly distinguished from all the rest of the globe by the entire absence of all the orders of non-aquatic mammalia that abound in the Old World, except two--the winged bats (Chiroptera), and the equally cosmopolite rodents (Rodentia). Of these latter however, only one family is represented--the Muridæ--(comprising the rats and mice), and the Australian representatives of these are all of small or moderate size--a suggestive fact in appreciating the true character of the Australian fauna. In place of the Quadrumana, Carnivora, and Ungulates, which abound in endless variety in all the other regions under equally favourable conditions, Australia possesses two new orders (or perhaps {391}sub-classes)--Marsupialia and Monotremata, found nowhere else on the globe except a single family of the former in America. The Marsupials are wonderfully developed in Australia, where they exist in the most diversified forms, adapted to different modes of life. Some are carnivorous, some herbivorous; some arboreal, others terrestrial. There are insect-eaters, root-gnawers, fruit-eaters, honey-eaters, leaf or grass-feeders. Some resemble wolves, others marmots, weasels, squirrels, flying squirrels, dormice or jerboas. They are classed in six distinct families, comprising about thirty genera, and subserve most of the purposes in the economy of nature, fulfilled in other parts of the world by very different groups; yet they all possess common peculiarities of structure and habits which show that they are members of one stock, and have no real affinity with the Old-World forms which they often outwardly resemble. The other order, Monotremata, is only represented by two rare and very remarkable forms, _Ornithorhynchus_ and _Echidna_, probably the descendants of some of those earlier developments of mammalian life which in every other part of the globe have long been extinct. The bats of Australia all belong to Old-World genera and possess no features of special interest, a result of the wandering habits of these aerial mammals. The Rodents are more interesting. They are all more or less modified forms of mice or rats. Some belong to the widely distributed genus _Mus_, others to four allied genera, which may be all modifications of some common Old-World form. They spread all over Australia, and allied species occur in Celebes and the Papuan Islands, so that although not yet known from the Moluccas, there can be little doubt that some of them exist there. _Birds._--The typical Australian region, as above defined, is almost as well characterized by its birds, as by its mammalia; but in this case the deficiencies are less conspicuous, while the peculiar and characteristic families are numerous and important. The most marked deficiency as regards wide-spread families, is the total absence of Fringillidæ (true finches), Picidæ (woodpeckers), Vulturidæ (vultures), and Phasianidæ (pheasants). {392}and among prevalent Oriental groups, Pycnonotidæ (bulbuls), Phyllornithidæ (green bulbuls), and Megalæmidæ (barbets) are families whose absence is significant. Nine families are peculiar to the region, or only just pass its limits in the case of single species. These are Paridiseidæ (paradise-birds), Meliphagidæ (honey-suckers), Menuridæ (lyre-birds), Atrichidæ (scrub-birds), Cacatuidæ (cockatoos), Platycercidæ (broad-tailed and grass-paroquets), Trichoglossidæ (brush-tongued paroquets), Megapodiidæ (mound-makers), and Casuariidæ (cassowaries). There are also eight very characteristic families, of which four,--Pachycephalidæ (thick-headed shrikes), Campephagidæ (caterpillar shrikes), Dicæidæ (flower-peckers), and Artamidæ (swallow-shrikes)--are feebly represented elsewhere, while the other four--Ploceidæ (weaver-finches), Alcædinidæ (kingfishers), Podargidæ (frog-mouths), and Columbidæ (pigeons)--although widely distributed, are here unusually abundant and varied, and (except in the case of the Ploceidæ) better represented in the Australian than in any other region. Of all these the Meliphagidæ (honeysuckers) are the most peculiarly and characteristically Australian. This family abounds in genera and species; it extends into every part of the region from Celebes and Lombock on the west, to the Sandwich Islands, Marquesas, and New Zealand on the east, while not a single species overpasses its limits, with the exception of one (_Ptilotis limbata_) which abounds in all the islands of the Timorese group, and has crossed the narrow strait from Lombock to Baly; but this can hardly be considered to impugn the otherwise striking fact of wide diffusion combined with strict limitation, which characterizes it. This family is the more important, because, like the Trichoglossidæ or brush-tongued paroquets, it seems to have been developed in co-ordination with that wealth of nectariferous flowering shrubs and trees which is one of the marked features of Australian vegetation. It probably originated in the extensive land-area of Australia itself, and thence spread into all the tributary islands, where it has become variously modified, yet always in such close adaptation to the other great features of the Australian fauna, that it seems unable to maintain itself when subject to the competition of the more {393}varied forms of life in the Oriental region; to which, possessing great powers of flight, some species must occasionally have emigrated. Its presence or absence serves therefore to define and limit the Australian region with a precision hardly to be equalled in the case of any other region or any other family of birds. The Trichoglossidæ, as already intimated, are another of these peculiarly organized Australian families,--parrots with an extensile brush-tipped tongue, adapted to extract the nectar and pollen from flowers. These are also rigidly confined to this region, but they do not range so completely over the whole of it, being absent from New Zealand (where however they are represented by a closely allied form _Nestor_), and from the Sandwich Islands. The Paradiseidæ (birds of paradise and allies) are another remarkable family, confined to the Papuan group of Islands, and the tropical parts of Australia. The Megapodiidæ (or mound-builders) are another most remarkable and anomalous group of birds, no doubt specially adapted to Australian conditions of existence. Their peculiarity consists in their laying enormous eggs (at considerable intervals of time) and burying them either in the loose hot sand of the beach above high-water mark, or in enormous mounds of leaves, sticks, earth, and refuse of all kinds, gathered together by the birds, whose feet and claws are enlarged and strengthened for the work. The warmth of this slightly fermenting mass hatches the eggs; when the young birds work their way out, and thenceforth take care of themselves, as they are able to run quickly, and even to fly short distances, as soon as they are hatched. This may perhaps be an adaptation to the peculiar condition of so large a portion of Australia, in respect to prolonged droughts and scanty water-supply, entailing a periodical scarcity of all kinds of food. In such a country the confinement of the parents to one spot during the long period of incubation would often lead to starvation, and the consequent death of the offspring. But the same birds with free power to roam about, might readily maintain themselves. This peculiar constitution and habit, which enabled the Megapodii to maintain an existence under the unfavourable conditions of their {394}original habitat gives them a great advantage in the luxuriant islands of the Moluccas, to which they have spread. There they abound to a remarkable extent, and their eggs furnish a luxurious repast to the natives. They have also reached many of the smallest islets, and have spread beyond the limits of the region to the Philippines, and North-Western Borneo, as well as to the remote Nicobar Islands. The Platycercidæ, or broad-tailed paroquets, are another wide-spread Australian group, of weak structure but gorgeously coloured, ranging from the Moluccas to New Zealand and the Society Islands, and very characteristic of the region, to which they are strictly confined. The Cockatoos have not quite so wide a range, being confined to the Austro-Malayan and Australian sub-regions, while one species extends into the Philippine Islands. The other two peculiar families are more restricted in their range, and will be noticed under the sub-regions to which they respectively belong. Of the characteristic families, the Pachycephalidæ, or thick-headed shrikes, are especially Australian, ranging over all the region, except New Zealand; while only a single species has spread into the Oriental, and one of doubtful affinity to the Ethiopian region. The Artamidæ, or swallow-shrikes, are also almost wholly confined to the region, one species only extending to India. They range to the Fiji Islands on the east, but only to Tasmania on the south. These two families must be considered as really peculiar to Australia. The Podargidæ, or frog-mouths--large, thick-billed goat-suckers--are strange birds very characteristic of the Australian region, although they have representatives in the Oriental and Neotropical regions. Campephagidæ (caterpillar-shrikes) also abound, but they are fairly represented both in India and Africa. The Ploceidæ, or weaver-birds, are the finches of Australia, and present a variety of interesting and beautiful forms. We now come to the kingfishers, a cosmopolitan family of birds, yet so largely developed in the Australian region as to deserve special notice. Two-thirds of all the genera are found here, and no less than 10 out of the 19 genera in the family are {395}peculiar to the Australian region. Another of the universally distributed families which have their metropolis here, is that of the Columbidæ or pigeons. Three-fourths of the genera have representatives in the Australian region, while two-fifths of the whole are confined to it; and it possesses as many species of pigeons as any other two regions combined. It also possesses the most remarkable forms, as exemplified in the great crowned pigeons (_Goura_) and the hook-billed _Didunculus_, while the green fruit-pigeons (_Ptilopus_) are sometimes adorned with colours vying with those of the gayest parrots or chatterers. This enormous development of a family of birds so defenceless as the pigeons, whose rude nests expose their eggs and helpless young to continual danger, may perhaps be correlated, as I have suggested elsewhere (Ibis, 1865, p. 366), with the entire absence of monkeys, cats, lemurs, weasels, civets and other arboreal mammals, which prey on eggs and young birds. The very prevalent green colour of the upper part of their plumage, may be due to the need of concealment from their only enemies,--birds of prey; and this is rendered more probable by the fact that it is among the pigeons of the small islands of the Pacific (where hawks and their allies are exceedingly scarce) that we alone meet with species whose entire plumage is a rich and conspicuous yellow. Where the need of concealment is least, the brilliancy of colour has attained its maximum. We may therefore look upon the genus _Ptilopus_, with its fifty species whose typical coloration is green, with patches of bright blue, red, or yellow on the head and breast, as a special development suited to the tropical portion of the Australian region, to which it is almost wholly confined. It will be seen from the sketch just given, that the ornithological features of the Australian region are almost as remarkable as those presented by its Mammalian fauna; and from the fuller development attained by the aërial class of birds, much more varied and interesting. None of the other regions of the earth can offer us so many families with special points of interest in structure, or habits, or general relations. The paradise-birds, the honeysuckers, the brush-tongued paroquets, the mound-builders, and the cassowaries--all strictly peculiar {396}to the region--with such remarkable developments as we have indicated in the kingfishers and pigeons, place the Australian region in the first rank for the variety, singularity, and interest of its birds, and only second to South America as regards numbers and beauty. _Reptiles._--In Reptiles the peculiarity of the main Australian region is less marked, although the fauna is sufficiently distinct. There is no family of snakes confined to the region, but many peculiar genera of the families Pythonidæ and Elapidæ. About two-thirds of the Australian snakes belong to the latter family, and are poisonous; so that although the Crotalidæ and Viperidæ are absent, there are perhaps a larger proportion of poisonous to harmless snakes than in any other part of the world. According to Mr. Gerard Krefft the proportion varies considerably in the different colonies. In Victoria, New South Wales, and Queensland the proportion is about two to one; in West Australia three to one; and in South Australia six to one. In Tasmania there are only 3 species and all are poisonous. The number of species, as in other parts of the world, seems to increase with temperature. The 3 in Tasmania have increased to 12 in Victoria, 15 in South Australia and the same in West Australia; 31 in New South Wales, and 42 in sub-tropical Queensland. The lizards of Australia have lately been catalogued by Dr. Günther in the concluding part of the "Voyage of the Erebus and Terror," issued in 1875. They belong to 8 families, 3 of which are peculiar; 57 genera of which 36 are peculiar; and about 140 species, all but 2 or 3 of which are peculiar. The scinks and geckoes form the great bulk of the Australian lizards, with a few Agamidæ, Gymnopthalmidæ, and Varanidæ. The three peculiar families are the Pygopodidæ, Aprasiidæ and Lialidæ; comprising only 4 genera and 7 species. The above all belong to Australia proper. Those of the other sub-regions are few in number and will be noticed under their respective localities. They will perhaps bring up the number of genera to 70. West and South Australia seem to offer much peculiarity in their lizards; these districts possessing 12 peculiar genera, {397}while a much smaller number are confined to the East and South-East, or to the North. Among the fresh-water turtles of the family Chelydidæ there are three peculiar genera--_Chelodina_, _Chelemys_, and _Elseya_, all from Australia. _Amphibia._--No tailed amphibians are known from the whole region, but no less than eleven of the families of tail-less Batrachians (toads and frogs) are known to inhabit some part or other of it. A peculiar family (Xenorhinidæ), consisting of a single species, is found in New Guinea; the true toads (Bufonidæ) are only represented by a single species of a peculiar genus in Australia, and by a _Bufo_ in Celebes. Nine of the families are represented in Australia itself, and the following genera are peculiar to it:--_Pseudophryne_ (Phryniscidæ), _Pachybatrachus_, and _Chelydobatrachus_ (Engystomydæ); _Helioporus_ (Alytidæ); _Pelodyras_ and _Chirodyras_ (Pelodryadæ); _Notaden_ (Bufonidæ). _Fresh-water Fish._--There is only one peculiar family of fresh-water fishes in this region--the Gadopsidæ--represented by a single genus and species. The other species of Australia belong to the families Trachinidæ, Atherinidæ, Mugillidæ, Siluridæ, Homalopteræ, Haplochitonidæ, Galaxidæ, Osteoglossidæ, Symbranchidæ, and Sirenoidei; most of the genera being peculiar. The large and widely-distributed families, Cyprinodontidæ and Cyprinidæ, are absent. The most remarkable fish is the recently discovered _Ceratodus_, allied to the _Lepidosiren_ of Tropical America, and _Protopterus_ of Tropical Africa, the three species constituting the Sub-class Dipnoi, remains of which have been found fossil in the Triassic formation. _Summary of Australian Vertebrata._--In order to complete our general sketch of Australian zoology, and to afford materials for comparison with other regions, we will here summarize the distribution of Vertebrata in the entire Australian region, as given in detail in the tables at the end of this chapter. When an undoubted Oriental family or genus extends to Celebes only we do not count it as belonging to the Australian region, that island being so very anomalous and intermediate in character. {398}The Australian region, then, possesses examples of 18 families of Mammalia, 8 of which are peculiar; 71 of Birds, 16 being peculiar; 31 of Reptiles, 4 being peculiar; 11 of Amphibia, with 1 peculiar; and 11 of Fresh-water fish, with 1 peculiar. In all, 142 families of Vertebrates, 30 of which are almost or quite confined to it, or between one-fourth and one-fifth of the whole number. The genera of Mammalia occurring within the limits of this region are 70, of which 45 are almost, or quite, confined to it. Of Land-Birds there are 296 genera, 196 of which are equally limited. The proportion is in both cases very nearly five-eighths. This shows a considerable deficiency both in families of Vertebrates and genera of Mammalia, as compared with the Oriental and Ethiopian regions; while in genera of Birds it is a little superior to the latter in total numbers, and considerably so in the proportion of peculiar types. _Supposed Land Connection between Australia and South America._ We may now consider how far the different classes and orders of vertebrates afford indications that during past ages there has been some closer connection between Australia and South America than that which now exists. Among Mammalia we have the remarkable fact of a group of marsupials inhabiting South America, and extending even into the temperate regions of North America, while they are found in no other part of the globe beyond the limits of the Australian region; and this has often been held to be evidence of a former connection between the two countries. A preliminary objection to this view is, that the opossums seem to be rather a tropical group, only one species reaching as far as 42° south latitude on the west coast of South America; but whatever evidence we have which seems to require a former union of these countries shows that it took place, if at all, towards their cold southern limits, the tropical faunas on the whole showing no similarity. This is not a very strong objection, since climates may have changed in the south to as great an extent as we {399}know they have in the north. Perhaps a more important consideration is, that _Didelphys_ is a family type unknown in Australia; and this implies that the point of common origin is very remote in geological time. But the most conclusive fact is that in the Eocene and Miocene periods this very family, Didelphyidæ, existed in Europe, while it only appeared in America in the Post-pliocene or perhaps the Pliocene period; so that it is really an Old-World group, which, though long since extinct in its birthplace, has survived in America, to which country it is a comparatively recent emigrant. Primeval forms of marsupials we know abounded in Europe during much of the Secondary epoch, and no doubt supplied Australia with the ancestors of the present fauna. It is clear, therefore, that in this case there is not a particle of evidence for any former union between Australia and South America; while it is almost demonstrated that both derived their marsupials from a common source in the northern hemisphere. Birds offer us more numerous but less clearly defined cases of this kind. Among Passeres, the wonderful lyre bird (_Menura_) is believed by some ornithologists to be decidedly allied to the South American Pteroptochidæ, while others maintain that it is altogether peculiar, and has no such affinity. The Australian Pachycephalidæ have also been supposed to find their nearest allies in the American Vireonidæ, but this is, perhaps, equally problematical. That the mound-makers (Megapodiidæ) of the Australian region are more nearly allied to the South American curassows (Cracidæ) than to any other family, is perhaps better established; but if proved, it is probably due, as in the case of the marsupials, to the survival of an ancient and once wide-spread type, and thus lends no support to the theory of a land connection between the two regions. A recent author, Professor Garrod, classes _Phaps_ and other Australian genera of pigeons along with _Zenaida_ and allied South American forms; but here again the affinity, if it exists, is so remote that the explanation already given will suffice to account for it. There remain only the penguins of the genus _Eudyptes_; and these have almost certainly passed from one region to the other, but {400}no actual land connection is required for birds which can cross considerable arms of the sea. Reptiles again seem to offer no more support to the view than do mammalia or birds. Among snakes there are no families in common that have not a very wide distribution. Among lizards the Gymnopthalmidæ are the only family that favour the notion, since they are found in Australia and South America, but not in the Oriental region. Yet they occur in both the Palæarctic and Ethiopian regions, and their distribution is altogether too erratic to be of any value in a case of this kind; and the same remarks apply to the tortoises of the family Chelydidæ. The Amphibia, however, furnish us with some more decided facts. We have first the family of tree-frogs, Pelodryade, confined to the two regions; _Litoria_, a genus of the family Hylidæ peculiar to Australia, but with one species in Paraguay; and in the family Discoglossidæ, the Australian genus _Chiroleptes_ has its nearest ally in the Chilian genus _Calyptocephalus_. Fresh-water fishes give yet clearer evidence. Three groups are exclusively found in these two regions; _Aphritis_, a fresh-water genus of Trachinidæ, has one species in Tasmania and two others in Patagonia; the Haplochitonidæ inhabit only Terra del Fuego, the Falkland Islands and South Australia; while the genus _Galaxias_ (forming the family Galaxidæ) is confined to South Temperate America, Australia, and New Zealand. We have also the genus _Osteoglossum_ confined to the tropical rivers of Eastern South America, the Indo-Malay Islands and Australia. It is important here to notice that the heat-loving Reptilia afford hardly any indications of close affinity between the two regions, while the cold-enduring amphibia and fresh-water fish, offer them in abundance. Taking this fact in connection with the absence of all indications of close affinity among the mammalia and terrestrial birds, the conclusion seems inevitable that there has been no land-connection between the two regions within the period of existing species, genera, or families. Yet some interchange of amphibia and fresh-water {401}fishes, as of plants and insects, has undoubtedly occurred, but this has been effected by other means. If we look at a globe we see at once how this interchange may have taken place. Immediately south of Cape Horn we have the South Shetland Islands and Graham's land, which is not improbably continuous, or nearly so, with South Victoria land immediately to the south of New Zealand. The intervening space is partly occupied by the Auckland, Campbell, and Macquaries' Islands, which, there is reason to believe are the relics of a great southern extension of New Zealand. At all events they form points which would aid the transmission of many organisms; and the farthest of the Macquaries' group, Emerald Island, is only 600 miles from the outlying islets of Victoria land. The ova of fish will survive a considerable time in the air, and the successful transmission of salmon ova to New Zealand packed in ice, shows how far they might travel on icebergs. Now there is evidently some means by which ova or young fishes are carried moderate distances, from the fact that remote alpine lakes and distinct river systems often have the same species. Glaciers and icebergs generally have pools of fresh water on their surfaces; and whatever cause transmits fish to an isolated pond might occasionally stock these pools, and by this means introduce the fishes of one southern island into another. Batrachians, which are equally patient of cold, might be transported by similar means; while, as Mr. Darwin has so well shown, (_Origin of Species_, 6th Ed. p. 345) there are various known modes by which plants might be transmitted, and we need not therefore be surprised that botanists find a much greater similarity between the production of the several Southern lands and islands, than do zoologists. It is important to notice that, however this intercommunication was effected, it has continued down to the epoch of existing species; for Dr. Günther finds the same species of fresh-water fish (_Galaxias attenuatus_) inhabiting Tasmania, New Zealand, the Falkland Islands, and Temperate South America; while another species is common to New Zealand and the Auckland Islands. We cannot believe that a land connection has existed between all these remote lands within the period of existence of this one species of fish, {402}not only on account of what we know of the permanence of continents and deep oceans, but because such a connection must have led to much more numerous and important cases of similarity of natural productions than we actually find. And if within the life of _species_ such interchange may have taken place across seas of greater or less extent, still more easy is it to understand, how, within the life of _genera_ and _families_, a number of such interchanges may have occurred; yet always limited to those groups whose conditions of life render transmission possible. Had an actual land connection existed within the temperate zone, or during a period of warmth in the Antarctic regions, there would have been no such strict limitations to the inter-migration of animals. It may be held to support the view that floating ice has had _some_ share in the transmission of fish and amphibia, when we find that in the case of the narrow tropical sea dividing Borneo from Celebes and the Moluccas, no proportionate amount of transmission has taken place, but numerous species, genera, and whole families, terminate abruptly at what we have other reasons for believing to be the furthest limits of an ancient continent. We can hardly suppose, however, that this mode of transmission would have sufficed for such groups as tree-frogs, which are inhabitants of the more temperate or even warm portions of the two southern lands. Some of these cases may perhaps be explained by the supposition of a considerable extent of land in the South-Temperate and Antarctic regions now submerged, and by a warm or temperate climate analogous to that which prevailed in the Arctic regions during some part of the Miocene epoch; while others may be due to cases of survival in the two areas of once wide-spread groups, a view supported in the case of the Amphibia by the erratic manner in which many of the groups are spread over the globe. From an examination of the facts presented by the various classes of vertebrates, we are, then, led to the conclusion, that there is no evidence of a former land-connection between the Australian and Neotropical regions; but that the various scattered resemblances in their natural productions {403}that undoubtedly occur, are probably due to three distinct causes. First, we have the American Didelphyidæ, among Mammals, and the Cracidæ, among birds, allied respectively to the Marsupials and the Megapodiidæ of Australia. This is probably more a coincidence than an affinity, due to the preservation of ancient wide-spread types in two remote areas, each cut off from the great northern continental masses, in which higher forms were evolved leading to the extinction of the lower types. In each of these southern isolated lands the original type would undergo a special development; in the one case suited to an arboreal existence, in the other to a life among arid plains. The second case is that of the tree-frogs, and the genus _Osteoglossum_ among fishes; and is most likely due to the extension and approximation of the two southern continents, and the existence of some intermediate lands, during a warm period when facilities would be afforded for the transmission of a few organisms by the causes which have led to the exceptional diffusion of fresh-water productions in all parts of the world. As however _Osteoglossum_ occurs also in the Sunda Islands, this may be a case of survival of a once wide-spread group. The third case is that of the same genera and even species of fish, and perhaps of frogs, in the two countries; which may be due to transmission from island to island by the aid of floating ice, with or without the assistance of more intervening lands than now exist. Having arrived at these conclusions from a consideration of the vertebrata, we shall be in a position to examine how far the same causes will explain, or agree with, the distribution of the invertebrate groups, or elucidate any special difficulties we may meet with in the relations of the sub-regions. _Insects._ The insects of the Australian region are as varied, and in some respects as peculiar as its higher forms of life. As we have already indicated in our sketch of the Oriental region, a vast number of forms inhabit the Austro-Malay sub-region {404}which are absent from Australia proper. Such of these as are common to the Malay archipelago as a whole, have been already noted; we shall here confine ourselves more especially to the groups peculiar to the region, which are almost all either Australian or Austro-Malayan, the Pacific Islands and New Zealand being very poor in insect life. _Lepidoptera._--Australia itself is poor in butterflies, except in its northern and more tropical parts, where green _Ornithopteræ_ and several other Malayan forms occur. In South Australia there are less than thirty-five species, whereas in Queensland there are probably over a hundred. The peculiar Australian forms are few. In the family Satyridæ, _Xenica_ and _Heteronympha_, with _Hypocista_ extending to New Guinea; among the Lycænidæ, _Ogyris_ and _Utica_ are confined to Australia proper, and _Hypochrysops_ to the region; and in Papilionidæ, the remarkable _Eurycus_ is confined to Australia, but is allied to _Euryades_, a genus found in Temperate South America (La Plata), and to the _Parnassius_ of the North-Temperate zone. The Austro-Malay sub-region has more peculiar forms. _Hamadryas_, a genus of Danaidæ, approximates to some South American forms; _Hyades_ and _Hyantis_ are remarkable groups of Morphidæ; _Mynes_ and _Prothoë_ are fine Nymphalidæ, the former extending to Queensland; _Dicallaneura_, a genus of Erycinidæ, and _Elodina_, of Pieridæ, are also peculiar forms. The fine _Ægeus_ group of _Papilio_, and _Priamus_ group of _Ornithoptera_, also belong exclusively to this region. _Xois_ is confined to the Fiji Islands, _Bletogona_ to Celebes, and _Acropthalmia_ to New Zealand, all genera of Satyridæ. Seventeen genera in all are confined to the Australian region. Among the Sphingina, _Pollanisus_, a genus of Zygænidæ, is Australian; also four genera of Castniidæ--_Synemon_, _Euschemon_, _Damias_, and _Cocytia_, the latter being confined to the Papuan islands. The occurrence of this otherwise purely South American family in the Australian region, as well as the affinity of _Eurycus_ and _Euryades_ noticed above, is interesting; but as we have seen that the genera and families of insects are more permanent than those of the higher animals, and as the groups in question are {405}confined to the warmer parts of both countries, they may be best explained as cases of survival of a once wide-spread type, and may probably date back to the period when the ancestors of the Marsupials and Megapodii were cut off from the rest of the world. _Coleoptera._--The same remark applies here as in the Lepidoptera, respecting the affinity of the Austro-Malay fauna to that of Indo-Malay Islands; but Australia proper is much richer in beetles than in butterflies, and exhibits much more speciality. Although the other two parts of the Australian region (Polynesia and New Zealand) are very poor in beetles, it will, nevertheless, on the whole compare favourably with any of the regions except the very richest. Cicindelidæ are not very abundant. _Therates_ and _Tricondyla_ are the characteristic genera in Austro-Malaya, but are absent from Australia, where we have _Tetracha_ as the most characteristic genus, with one species of _Megacephala_ and two of _Distypsidera_, a genus which is found also in New Zealand and some of the Pacific Islands. The occurrence of the South American genus, _Tetracha_, may perhaps be due to a direct transfer by means of intervening lands during the warm southern period; but considering the permanence of coleopterous forms (as shown by the Miocene species belonging almost wholly to existing genera), it seems more probable that it is a case of the survival of a once wide-spread group. Carabidæ are well represented, there being no less than 94 peculiar genera, of which 19 are confined to New Zealand. The Australian genera of most importance are _Carenum_ (68 species), _Promecoderus_ (27 species), _Silphomorpha_ (32 species), _Adelotopus_ (27 species), _Scaraphites_ (25 species), _Notonomus_ (18 species), _Gnathoxys_ (12 species), _Eutoma_ (9 species), _Ænigma_ (15 species), _Lacordairea_ (8 species), _Pamborus_ (8 species), _Catadromus_ (4 species),--the latter found in Australia and Celebes. Common to Australia and New Zealand are _Mecodema_ (14 species), _Homalosoma_ (32 species), _Dicrochile_ (12 species), and _Scopodes_ (5 species). The larger genera, confined to New Zealand only, are _Metaglymma_ (8 species), and _Demetrida_ (3 species). The curious genus _Pseudomorpha_ (10 species), is divided between California, Brazil, {406}and Australia; and the Australian genera, _Adelotopus_, _Silphomorpha_, and _Sphallomorpha_, form with it a distinct tribe of Coleoptera. These being all confined to the warmer regions, and having so scattered a distribution, are no doubt the relics of a widespread group. The Australian genus, _Promecoderus_, has, however, closely allied genera (_Cascelius_ and its allies), in Chili and Patagonia; while two small genera confined to the Auckland Islands (_Heterodactylus_ and _Pristancyclus_) are allied to a group found only in Terra-del-Fuego and the Falkland Islands, (_Migadops_); and in these cases we may well believe that a direct transmission has taken place by some of the various means already indicated. In Lucanidæ, Australia is only moderately rich, having 7 peculiar genera. The most important are _Ceratognathus_ and _Rhyssonotus_, confined to Australia; _Lissotes_ to Australia and New Zealand; _Lamprima_ to Australia and Papua. _Mitophyllus_ and _Dendroblax_ inhabit New Zealand only; while _Syndesus_ is found in Australia, New Caledonia, and tropical South America. The beautiful Cetoniidæ are poorly represented, there being only 3 peculiar genera;--_Schizorhina_, mainly Australian, but extending to Papua and the Moluccas; _Anacamptorhina_, confined to New Guinea, and _Sternoplus_ to Celebes. _Lomaptera_ is very characteristic of the Austro-Malay Islands. This almost tropical family shows no approximations between the Australian and Neotropical faunas. In Buprestidæ, the Australian region is the richest, possessing no less than 47 genera, of which 20 are peculiar to it. Of these, 15 are peculiar to Australia itself, the most important being _Stigmodera_ (212 species), _Ethon_ (13 species), and _Nascio_ (3 species); _Cisseis_ (17 species), and the magnificent _Calodema_ (3 species), are common to Australia and Austro-Malaya; while _Sambus_ (10 species) and _Anthaxomorpha_ (4 species), with some smaller groups, are peculiarly Austro-Malayan. In this family occur several points of contact with the Neotropical region. _Stigmodera_ is said to have a species in Chili, while there are undoubtedly several allied genera in Chili and South Temperate America. The genus _Curis_ has 5 Australian and 3 Chilian species, and {407}_Acherusia_ has 2 species in Brazil, 1 in Australia. These resemblances may probably have arisen from intercommunication during the warm southern period, when floating timber would occasionally transmit a few larvæ of this family from island to island across the antarctic seas. When the cold period returned, they would spread northward, and become more or less modified under the new physical conditions and organic competition, to which they were subjected. We now come to the very important group of Longicorns, in which the Australian region as a whole, is very rich, possessing 360 genera, of which 263 are peculiar to it. Of these about 50 are confined to the Austro-Malay Islands, 12 to New Zealand, and the remainder to Australia proper with Tasmania. Of the genera confined to, or highly characteristic of Australia, the following are the most important:--_Cnemoplites_, belonging to the Prionidæ; _Phoracantha_, to the Cerambycidæ; _Zygocera_, _Hebecerus_, _Symphyletes_, and _Rhytidophora_, to the Lamiidæ. Confined to the Austro-Malay Islands are _Tethionea_ (Cerambycidæ): _Tmesisternus_, _Arrhenotus_, _Micracantha_, and _Sybra_ (Lamiidæ); but there are also such Malayan genera as _Batocera_, _Gnoma_, _Praonetha_, and _Sphenura_, which are very abundant in the Austro-Malay sub-region. A species of each of the Australian genera, _Zygocera_, _Syllitus_, and _Pseudocephalus_, is said to occur in Chili, and one of the tropical American genus, _Hammatochærus_, in tropical Australia; an amount of resemblance which, as in the case of the Buprestidæ, may be imputed to trans-oceanic migration during the Southern warm period. This concludes our illustrations of the distribution of some of the more important groups of Australian insects; and it will be admitted that we have not met with any such an amount of identity with the fauna of Temperate South America, as to require us to modify the conclusions we arrived at from a consideration of the vertebrate groups. _Land-Shells._--The distribution of many of the larger genera of land-shells is very erratic, while others are exceedingly restricted, so that it requires an experienced conchologist to investigate the affinities of the several groups, and thus work {408}out the important facts of distribution. All that can be done here is to note the characteristic and peculiar genera, and any others presenting features of special interest. In the great family of the snails (Helicidæ), the only genera strictly confined to the region are, _Partula_, now containing above 100 species, and ranging over the Pacific from the Solomon Isles on the west, to the Sandwich Islands and Tahiti on the east; and _Achatinella_, now containing nearly 300 species, and wholly confined to the Sandwich Islands. _Pfeifferia_ is confined to the Philippine Islands and Moluccas; _Cochlostyla_ to the Indo-Malay Islands and Australia; _Bulimus_ occurs in most of the insular groups, including New Zealand, but is absent from Australia. Among the Aciculidæ, the widely-scattered _Truncatella_ is the only genus represented. Among Diplommatinidæ, _Diplommatina_ is the characteristic genus, ranging over the whole region, and found elsewhere as far as India, with one species in Trinidad. The extensive family Cyclostomidæ, is not well represented. Seven genera reach the Austro-Malay Islands, one of which, _Registoma_, is confined to the Philippines, Moluccas, New Caledonia, and the Marshall Islands. _Omphalotropis_ is the most characteristic genus, ranging over the whole region; _Callia_ is confined to the Philippines, Ceram, and Australia; _Realia_ to New Zealand and the Marquesas. The genus _Helicina_ alone represents the Helicinidæ, and is found in the whole region except New Zealand. The number of species known from Australia is perhaps about 300; while the Polynesian sub-region, according to Mr. Harper Pease, contains over 600; the Austro-Malay Islands will furnish probably 200; and New Zealand about 100; making a total of about 1,200 species for the whole region. AUSTRALIAN SUB-REGIONS. Few of the great zoological regions comprise four divisions so strongly contrasted as these, or which present so many interesting problems. We have first the Austro-Malay Islands, an equatorial forest-region teeming with varied and beautiful forms of life; next we have Australia itself, an island-continent with its satellite {409}Tasmania, both tropical and temperate, but for the most part arid, yet abounding in peculiar forms in all the classes of animals; then come the Polynesian Islands, another luxuriant region of tropical vegetation, yet excessively poor in most of the higher groups of animals as well as in some of the lower; and lastly, we have New Zealand, a pair of temperate forest-clad islands far in the southern ocean, with a very limited yet strange and almost wholly peculiar fauna. We have now to consider the general features and internal relations of the faunas of each of these sub-regions, together with any external relations which have not been discussed while treating the region as a whole. _I. Austro-Malayan Sub-region._ The central mass on which almost every part of this sub-region is clearly dependent, is the great island of New Guinea, inhabited by the Papuan race of mankind; and this, with the surrounding islands, which are separated from it by shallow seas and possess its most marked zoological features, are termed Papua. A little further away lie the important groups of the Moluccas on one side and the Eastern Papuan Islands on the other, which possess a fauna mainly derivative from New Guinea, yet wanting many of its distinctive types; and, in the case of the Moluccas possessing many groups which are not Australian, but derived from the adjacent Oriental region. To the south of these we have the Timor group, whose fauna is clearly derivative, from Australia, from Java, and from the Moluccas. Lastly comes Celebes, whose fauna is most complex and puzzling, and, so far as we can judge, not fundamentally derivative from any of the surrounding islands. _Papua, or the New Guinea Group._--New Guinea is very deficient in Mammalia as compared with Australia, though this apparent poverty may, in part, depend on our very scanty knowledge. As yet only four of the Australian families of Marsupials are known to inhabit it, with nine genera, several of which are peculiar. It also possesses a peculiar form of wild pig; but as yet no other non-marsupial terrestrial mammal has been discovered, except a rat, described by Dr. Gray as _Uromys {410}aruensis_, but about the locality of which there seems some doubt.[13] Omitting bats, of which our knowledge is very imperfect, the Papuan Mammals are as follows:-- Family. Genus. Species. Suidæ _Sus_ 1 Eastern limit of the genus. Muridæ _Uromys_ 1 Aru Islands (?) Dasyuridæ _Phascogale_ 1 Australian genus. " _Antechinus_ 1 " " " _Dactylopsila_ 1 To North Australia only. " _Myoictis_ 1 Aru islands only. Peramelidæ _Perameles_ 1 New Guinea only. Macropodidæ _Dendrolagus_ 2 New Guinea only. " _Dorcopsis_ 2 Papua only. Phalangistidæ _Cuscus_ 7 Celebes to New Guinea. " _Belideus_ 1 Australia and Moluccas. We have here no sign of any approach to the Mammalian fauna of the Oriental region, for though _Sus_ has appeared, the Muridæ (rats and mice) seem to be wanting. In Birds the case is very different, since we at once meet with important groups, either wholly, or almost peculiar to the Papuan fauna. According to a careful estimate, embodying the recent discoveries of Meyer and D'Albertis, there are 350 species of Papuan land-birds comprised in 136 genera. About 300 of the species are absolutely peculiar to the district, while 39 of the genera are exclusively Papuan or just extend into the Moluccas, or into North Australia where it closely approaches New Guinea. In analysing the genera we may set aside 31 as having a wide range, and being of no significance in distribution; such are most of the birds of prey, with the genera _Hirundo_, _Caprimulgus_, _Zosterops_; and others widely spread in both the Oriental and Australian regions, as _Dicæum_, _Munia_, _Eudynamis_, &c. Of the remainder, as above stated, about 39 are peculiar to the Papuan fauna, 50 are characteristic Australian genera; 9 are more especially Malayan, and as much Australian as Oriental; while 7 only, appear to be typically Oriental with a discontinuous distribution, none of them occurring in the Moluccas. {411}This Papuan fauna is so interesting and remarkable, that it seems advisable to give lists of these several classes of generic types. I. Genera occurring in the Papuan Islands which are characteristic of the Australian region (89). Those marked with an asterisk are exclusively Papuan. Sylviidæ _Malurus_, _Gerygone_, _Petroica_, _Orthonyx_. Certhiidæ _Climacteris_. Sittidæ _Sittella_. Oriolidæ _Mimeta_. Campephagidæ _Graucalus_, _Lalage_. Dicruridæ *_Chætorhynchus_. Muscicapidæ *_Peltops_, _Monarcha_, *_Leucophantes_, _Microeca_, _Sisura_, _Myiagra_, *_Machærirhynchus_, _Rhipidura_, *_Todopsis_. Pachycephalidæ _Pachycephala_. Laniidæ *_Rectes_. Corvidæ _Cracticus_, *_Gymnocorvus_. Paradiseidæ *_Paradisea_, *_Manucodia_, *_Astrapia_, *_Parotia_, *_Lophorina_, *_Diphyllodes_, *_Xanthomelus_, *_Cicinnurus_, *_Paradigalla_, *_Epimachus_, *_Drepanornis_, *_Seleucides_, _Ptilorhis_, _Æluroedus_, *_Amblyornis_. Meliphagidæ _Myzomela_, _Entomophila_, _Glicyphila_, _Ptilotis_, *_Melidectes_, *_Melipotes_, *_Melirrhophetes_, _Anthochæra_, _Philemon_, *_Euthyrhynchus_, _Melithreptes_. Nectariniidæ _Chalcostetha_, *_Cosmetira_. Artamidæ _Artamus_. Pittidæ *_Melampitta_. Cuculidæ *_Caliechthrus_. Alcedinidæ _Alcyone_, *_Syma_, _Dacelo_, *_Tanysiptera_, *_Melidora_. Podargidæ _Podargus_, _Ægotheles_. Caprimulgidæ _Eurostopodus_. Cacatuidæ _Cacatua_, *_Microglossus_, _Licmetis_, *_Nasiterna_. Platycercidæ _Aprosmictus_ Palæornithidæ _Tanygnathus_, _Eclectus_, _Geoffroyus_, *_Cyclopsitta_. Trichoglossidæ _Trichoglossus_, *_Charmosyna_, _Eos_, _Lorius_. Nestoridæ *_Dasyptilus_. Columbidæ _Ptilopus_, _Carpophaga_, _Ianthoenas_, _Reinwardtoenas_, *_Trugon_, *_Henicophaps_, _Phlogoenas_, *_Otidiphaps_, *_Goura_. Megapodiidæ _Talegallus_, _Megapodius_. Falconidæ *_Henicopernis_. Casuariidæ _Casuarius_. The chief points of interest here are the richness and specialization of the parrots, pigeons, and kingfishers; the wonderful paradise-birds; the honeysuckers; and some remarkable flycatchers. {412}The most prominent deficiencies, as compared with Australia, are in Sylviidæ, Timaliidæ, Ploceidæ, Platycercidæ, and Falconidæ. II. The genera which are characteristic of the whole Malay Archipelago are the following (10):-- 1. _Erythrura_ (Ploceidæ) 2. _Pitta_ (Pittidæ) 3. _Ceyx_ (Alcedinidæ) 4. _Calao_ (Bucerotidæ) 5. _Dendrochelidon_ (Cypselidæ) 6. _Loriculus_ (Psittacidæ) 7. _Macropygia_ (Columbidæ) 8. _Chalcophaps_ " 9. _Caloenas_ " 10. _Baza_ (Falconidæ) III. The curious set of genera apparently of Indo-Malayan origin, but unknown in the Moluccas, are as follows:-- 1. _Eupetes_ (Cinclidæ) 2. _Alcippe_ (Timaliidæ) 3. _Pomatorhinus_ " 4. _Arachnothera_ (Nectariniidæ) 5. _Prionochilus_ (Dicæidæ) 6. _Eulabes_ (Sturnidæ) The above six birds are very important as indicating past changes in the Austro-Malay Islands, and we must say a few words about each. (1) _Eupetes_ is very remarkable, since the New Guinea birds resemble in all important characters that which is confined to Malacca and Sumatra. They are probably the survivors of a once wide-spread Malayan group. (2) _Alcippe_ or _Drymocataphus_ (for in which genus the birds should be placed is doubtful) seems another clear case of a typical Indo-Malayan form occurring in New Guinea and Java, but in no intervening island. (3) _Pomatorhinus_ is a most characteristic Himalayan and Indo-Malayan genus, occurring again in New Guinea and also in Australia, but in no intermediate island. The New Guinea bird seems as nearly related to Oriental as Australian species. (4) _Arachnothera_ is exactly parallel to _Alcippe_, occurring nowhere east of Borneo except in New Guinea. (5) _Prionochilus_, a small black bird, sometimes classed as a distinct genus, but evidently allied to the _Prionochili_ of the Indo-Malay Islands. (6) _Eulabes_, the genus which contains the well known Mynahs of India, extends east of Java as far as Flores, but is not found in Celebes or the Moluccas. The two New Guinea species are sometimes classed in different genera, but they are undoubtedly allied to the Mynahs of India and Malaya. We find then, that while the ornithology of New Guinea is {413}preeminently Australian in character and possesses many peculiar developments of Australian types, it has also--as might be expected from its geographical position, its climate, and its vegetation--received an infusion of Malayan forms. But while one group of these is spread over the whole Archipelago, and occasionally beyond it, there is another group which presents the unusual and interesting feature of discontinuous distribution, jumping over a thousand miles of island-studded sea from Java and Borneo to New Guinea itself. It is a parallel case to that of Java in the Oriental region, which we have already discussed, but the suggested explanation in that case is more difficult to apply here. The recent soundings by the _Challenger_ show us, that although the several islands of the Moluccas are surrounded by water from 1,200 to 2,800 fathoms deep, yet these seas form inclosed basins with rims not more than from 400 to 900 fathoms deep, suggesting the idea of great lakes or inland seas which have sunk down bodily with the surrounding land, or that enormous local and restricted elevations and subsidences have here occurred. We have also the numerous small islands and coral banks south of Celebes and eastward towards Timor-Laut and the Aru Islands, indicating great subsidence; and it is possible that there was an extension of Papua to the west, approaching sufficiently near to Java to receive occasional straggling birds of Indo-Malay type, altogether independent of the Moluccas to the north. _Bright Colours and Ornamental Plumage of New Guinea Birds._--One of the most striking features of Papuan ornithology is the large proportion which the handsome and bright-coloured birds bear to the more obscure species. That this is really the case has been ascertained by going over my own collections, made at Aru and New Guinea, and comparing them with my collection made at Malacca--a district remarkable for the number of handsome birds it produces. Using, as nearly as possible, the same standard of beauty, about one-third of the Malacca birds may be classed as handsome,[14] while in Papua the proportion comes out exactly one-half. This is due, in part to the great abundance of {414}parrots, cockatoos, and lories, almost all of which are beautiful; and of pigeons, more than half of which are very beautiful; as well as to the numerous kingfishers, most of which are excessively brilliant. Then we have the absence of thrushes, and the very small numbers of the warblers, shrikes, and Timaliidæ, which are dull-coloured groups; and, lastly, the presence of numerous gay pittas, flycatchers, and the unequalled family of paradise-birds. A large number of birds adorned with metallic plumage is also a marked feature of this fauna, more than a dozen genera being so distinguished. Among the remarkable forms are _Peltops_, a flycatcher, long classed as one of the Indo-Malayan Eurylæmidæ, which it resembles both in bill and coloration; _Machærirhynchus_, curious little boat-billed flycatchers; and _Todopsis_, a group of terrestrial flycatchers with the brilliant colours of _Pitta_ or _Malurus_. The paradise-birds present the most wonderful developments of plumage and the most gorgeous varieties of colour, to be found among passerine birds. The great whiskered-swift, the handsomest bird in the entire family, has its head-quarters here. Among kingfishers the elegant long-tailed _Tanysipteræ_ are preeminent, whether for singularity or beauty. Among parrots, New Guinea possesses the great black cockatoo, one of the largest and most singular birds in the order; _Nasiterna_, the smallest of known parrots; and _Charmosyna_, perhaps the most elegant. Lastly, among the pigeons we have the fine crowned-pigeons, the largest and most remarkable group of the order. Plate X. [Illustration] SCENE IN NEW GUINEA, WITH CHARACTERISTIC ANIMALS. _Plate X. Illustrating the Ornithology of New Guinea._--The wonderful ornithological fauna we have just sketched, could only be properly represented in a series of elaborate coloured plates. We are obliged here to confine ourselves to representing a few of the more remarkable types of form, as samples of the great number that adorn this teeming bird-land. The large central figure is the fine twelve-wired paradise-bird (_Seleucides albus_), one of the most beautiful and remarkable of the family. Its general plumage appears, at first sight, to be velvety black; but on closer examination, and by holding the bird in various lights, it is found that every part of it glows with the most exquisite metallic tints--rich bronze, intense violet, and, on the {415}edges of the breast-feathers, brilliant green. An immense tuft of dense plumes of a fine orange-buff colour, springs from each side of the body, and six of these on each side terminate in a black curled rachis or shaft, which form a perfectly unique adornment to this lovely bird. To appreciate this wonderful family (of which no good mounted collection exists) the reader should examine the series of plates in Mr. Elliot's great work on the Paradiseidæ, where every species is figured of the size of life, and with a perfection of colouring that leaves little to be desired. Below the _Seleucides_ is one of the elegant racquet-tailed king-hunters (_Tanysiptera galatea_) whose plumage of vivid blue and white, and coral-red bill, combined with the long spatulate tail, renders this bird one of the most attractive of the interesting family of kingfishers. On a high branch is seated the little Papuan parroquet (_Charmosyna papuensis_), one of the Trichoglossidæ, or brush-tongued parrots,--richly adorned in red and yellow plumage, and with an unusually long and slender tail. On the ground is the well-known crowned pigeon (_Goura coronata_), a genus which is wholly confined to New Guinea and a few of the adjacent islands. One of the very few Papuan mammals, a tree-kangaroo (_Dendrolagus inustus_), is seated on a high branch. It is interesting, as an arboreal modification of a family which in Australia is purely terrestrial; and as showing how very little alteration of form or structure is needed to adapt an animal to such a different mode of life. _Reptiles and Amphibia._--Of these classes comparatively little is at present known, but there is evidence that the same intermixture of Oriental and Australian forms that occurs in birds and insects, is also found here. Dr. A. B. Meyer, the translator of this work into German, and well known for his valuable discoveries in New Guinea, has kindly furnished me with a manuscript list of Papuan reptiles, from which most of the information I am able to give is derived. Of Snakes, 24 genera, are known, belonging to 11 families. Six of the genera are Oriental,--_Calamaria_, _Cerberus_, _Chrysopelea_, _Lycodon_, _Chersydrus_, and _Ophiophagus_. Four are Australian,--_Morelia_, {416}_Liasis_, _Diemenia_, and _Acanthophis_; while four others are more especially Papuan,--_Dibamus_ (Typhlopidæ), _Brachyorros_--a sub-genus of the wide-spread _Rhabdosoma_ (Calamariidæ), found also in Timor; _Nardoa_ and _Enygrus_ (Pythonidæ), ranging from the Moluccas to the Fiji Islands. The rest are either common to the Oriental and Australian regions or of wide range. Of Lizards also, 24 genera are recorded, belonging to 5 families. Three only are peculiarly Oriental,--_Eumeces_, _Tiaris_, and _Nycteridium_; but another, _Gonyocephalus_, is Malayan, ranging from Java and Borneo to the Pelew Islands. Three are Australian,--_Cyclodus_, _Heteropus_, and _Gehyra_; while six are especially Papuan,--_Keneuxia_ (extending to the Philippines), _Elania_, _Carlia_ (to North Australia), _Lipinia_ (to the Philippine Islands), and _Tribolonotus_,--all belonging to the Scincidæ; and _Arua_ belonging to the Agamidæ. We must add _Cryptoblepharus_, which is confined to the Australian region, except a species in Mauritius. The other genera have a wider distribution. The preponderant Oriental element in the snakes as compared with the lizards, is suggestive of the dispersal of the former being dependent on floating trees, or even on native canoes, which for an unknown period have traversed these seas, and in which various species of snakes often secrete themselves. This seems the more probable, as snakes are usually more restricted in their range than lizards, and exhibit less numerous examples of widespread genera and species. The other orders of reptiles present no features of interest. Of Amphibia only 8 genera are known, belonging to 6 families. _Rana_, _Hylarana_, and _Hyla_ are wide-spread genera, the former being, however, absent from Australia. _Hyperolius_, _Pelodryas_, _Litoria_, and _Asterophrys_ are Australian; while _Platymantis_ is Polynesian, with a species in the Philippine Islands. Hence it appears that the amphibia, so far as yet known, exhibit no Oriental affinity; and this is a very suggestive fact. We have seen (p. 29) that salt water is almost a complete barrier to the dispersal of these creatures; so that the wholly Australian character of the Papuan batrachia is what we might expect, if, as here advocated, no actual land connection between {417}the Oriental and Australian regions, has probably occurred during the entire Tertiary and Post-tertiary periods. _Insects._--The general character of the Papuan insects has been sufficiently indicated in our sketch of the Entomology of the region. We will here only add, that the metallic lustre so prevalent among the birds, is also apparent in such insects as _Sphingnotus mirabilis_, a most brilliant metallic Longicorn; _Lomaptera wallacei_ and _Anacamptorhina fulgida_, Cetonii of intense lustre; _Calodema wallacei_ among the Buprestidæ; and the elegant blue _Eupholi_ among the weevils. Even among moths we have _Cocytia durvillii_, remarkable for its brilliant metallic colours. _The Moluccas._--The islands of Gilolo, Bouru, and Ceram, with several smaller islands adjacent, together with Sanguir, and perhaps Tulour or Salibaboo to the north-west, and the islands from Ke to Timor-Laut to the south-east, form the group of the Moluccas or Spice-Islands, remarkable for the luxuriance of their vegetation and the extreme beauty of their birds and insects. Their Mammalia are of Papuan character, with some foreign intermixture. Two genera of the New Guinea marsupials, _Belideus_ and _Cuscus_, abound; and we have also the wide-spread _Sus_. But besides these, we find no less than five genera of placental Mammals quite foreign to the Papuan or Australian faunas. These are 1. _Cynopithecus nigrescens_, found only in the small island of Batchian, and probably introduced from Celebes, where the same ape occurs. 2. _Viverra tangalunga_, a common Indo-Malayan species of civet, probably introduced. 3. _Cervus hippelaphus_, var. _Moluccensis_, a deer abundant in all the islands, very close to a Javan species and almost certainly introduced by man, perhaps very long ago. 4. _Babirusa alfurus_, the babirusa, found only in the island of Bouru, and perhaps originally introduced from Celebes. 5. _Sorex_ sp., small shrews. With the exception of the last, _all_ these species are animals habitually domesticated and kept in confinement by the Malays; and when we consider that none of the smaller Mammalia of Java and Borneo, numbering at least fifty different species, are found {418}in any of the Moluccas, we can hardly suppose that such large animals as the deer and ape, could have reached them by natural means. There is every reason to believe, therefore, that the indigenous Mammalia of the Moluccas are wholly of Papuan stock, and very limited in number. The birds are much more varied and interesting. About 200 species of land-birds are now known, belonging to 85 genera. Of the species about 15 are Indo-Malayan, 32 Papuan, and about 140 peculiar. Of the genera only two are peculiar,--_Semioptera_, a paradise bird, and _Lycocorax_, a singular form of Corvidæ; but there is also a peculiar rail-like wader, _Habroptila_. One genus, _Basilornis_, is found only in Ceram and Celebes; another, _Scythrops_, is Australian, and perhaps a migrant. About 30 genera are characteristic Papuan types, and 37 others, of more or less wide range, are found in New Guinea and were therefore probably derived thence. There remains a group of birds which are not found in New Guinea, and are either Palæarctic or Oriental. These are 13 in number as follows:-- 1. Monticola. 2. Acrocephalus. 3. Cisticola. 4. Hypolais. 5. Criniger. 6. Butalis. 7. Budytes. 8. Corydalla. 9. Hydrornis. 10. Batrachostomus. 11. Loriculus. 12. Treron. 13. Neopus. Of these the _Monticola_, found only in Gilolo, appears to be a straggler or migrant from the Philippine islands. _Acrocephalus_, of which four species occur, is a wide-spread group; one of the Moluccan birds is an Australian and another a North-Asian species, which perhaps indicates that there has long been some migration southward from island to island, across the Moluccas. _Cisticola_ is a genus of very wide range, extending to Australia. _Hypolais_ is probably a modified form of a Chinese or Javanese species. _Criniger_ is a pure Indo-Malay form, represented here by three fine species. _Butalis_ is a Chinese species, no doubt straggling southward. _Budytes_ and _Corydalla_ are widespread Oriental and Palæarctic species or slight modifications of them. _Hydrornis_ is a Malayan form of Pittidæ. _Batrachostomus_ is a distinct representative of a purely Indo-Malay genus. {419}_Loriculus_ is Malayan, and especially Philippine, but it reaches as far as Mysol. _Treron_ is here at its eastern limit, and is represented in Bouru and Ceram by one of the most beautiful species. _Neopus_, a Malayan eagle, is said to occur in the Moluccas. We find then only three characteristic Indo-Malay types in the Moluccas,--_Criniger_, _Batrachostomus_, and _Treron_. All are represented by distinct and well marked species, indicating a somewhat remote period since their ancestors entered the district, but all are birds of considerable powers of flight, so that a very little extension of the islands in a south-westerly direction would afford the means of transmission, but this could not well have been by way of Celebes, because the two former genera are unknown in that island. It is evident, therefore, that the Moluccas are wholly Papuan in their zoology; yet they are no less clearly derivative, and must have obtained their original immigrants under conditions that rendered a full representation of the fauna impossible. Such remarkable and dominant types as the eleven genera of Paradiseidæ, with _Cracticus_, _Rectes_, _Todopsis_, _Machærirhynchus_, _Gerygone_, _Dacelo_, _Podargus_, _Cyclopsitta_, _Microglossum_, _Nasiterna_, _Chalcopsitta_, and _Goura_,--all characteristic Papuan groups, found in almost all the islands and most of them very abundant, are yet totally absent from the Moluccas. Taking this, in conjunction with the absence of the two genera of Papuan kangaroos and the other smaller groups of marsupials, and we must be convinced that the Moluccas cannot be mere fragments of the old Papuan land, or they would certainly, in some one or other of their large and fertile islands, have preserved a more complete representation of the parent fauna. Most of the Moluccan birds are very distinct from the allied species of New Guinea; and this would imply that the entrance of the original forms took place at a remote period. The two peculiar genera with clearly Papuan affinities, show the same thing. The cassowary, found only in the large island of Ceram and distinct from any Papuan species, would however seem to have required a land connection for its introduction, almost as much as any of the larger mammalia. {420}Taking all the facts into consideration, I would suggest as the most probable explanation, that if the Moluccas ever formed part of the main Papuan land, they were separated at an early date, and subsequently so greatly submerged as to destroy a large proportion of their fauna. They have since risen, and have probably been larger than at present, and rather more closely approximated to the parent land, whence they received a considerable immigration of such animals as were adapted to cross narrow seas. This gave them several Papuan forms, but still left them without a number of the types more especially confined to the forest depths, or powerful enough to combat the gales which often blow weaker flyers out to sea. Most of the birds whose absence from the Moluccas is so conspicuous belong to one or other of these classes. Among the most characteristic birds of the Moluccas are the handsome crimson lories of the genera _Lorius_ and _Eos_. These are found in every island (but not in Celebes or the Timor group); and a fine species of _Eos_, peculiar to the small islands of Siau and Sanguir, just north of Celebes, obliges us to place these with the Moluccas instead of with the former island, to which they seem most naturally to belong. The crimson parrots of the genus _Eclectus_ are almost equally characteristic of the Moluccas, and add greatly to the brilliancy of the ornithology of these favoured islands. _Reptiles._--The Reptiles, so far as known, appear to agree in their distribution with the other vertebrates. In some small collections from Ceram there were no less than six of the genera peculiar to the Australian region, and which were before only known from Australia itself. These are, of snakes, _Liasis_ and _Enygrus_, genera of Pythonidæ; with _Diemenia_ and _Acanthophis_ (Elapidæ); of lizards, _Cyclodus_, a genus of Scincidæ; and of Amphibia, a tree-frog of the genus _Pelodryas_. _Insects--Peculiarities of the Moluccan Fauna._--In insects the Moluccas are hardly, if at all, inferior to New Guinea itself. The islands abound in grand _Papilios_ of the largest size and extreme beauty; and it is a very remarkable fact, that when the closely-allied species of the Moluccas and New Guinea are compared, {421}the former are almost always the largest. As examples may be mentioned, _Ornithoptera priamus_ and _O. helena_ of the Moluccas, both larger than the varieties (or species) of Papua; _Papilio ulysses_ and _deiphobus_ of Amboyna, usually larger than their allies in New Guinea; _Hestia idea_, the largest species of the genus; _Diadema pandarus_ and _Charaxes euryalus_, both larger than any other species of the same genera in the whole archipelago. It is to be noted also, that in the Moluccas, the very largest specimens or races seem always to come from the small island of Amboyna; even those of Ceram, the much larger island to which it is a satellite, being almost always of less dimensions. Among Coleoptera, the Moluccas produce _Euchirus longimanus_, one of the largest and most remarkable of the Lamellicornes; _Sphingnotus dunningi_, the largest of the Austro-Malayan Tmesisterninæ; a _Sphenura_, the largest and handsomest of an extensive genus; an unusually large _Schizorhina_ (Cetoniidæ); and some of the most remarkable and longest-horned Anthotribidæ. Even in birds the same law may be seen at work,--in the _Tanysiptera nais_ of Ceram, which has a larger tail than any other in the genus; in _Centropus goliath_ of Gilolo, being the largest and longest-tailed species; in _Hydrornis maximus_ of Gilolo, the largest and perhaps the most elegantly and conspicuously coloured of all the Pittidæ; in _Platycercus amboinensis_, being pre-eminent in its ample blue tail; in the two Moluccan lories and _Eos rubra_, being more conspicuously red than the allied New Guinea species; and in _Megapodius wallacei_ of Bouru, being the only species of the genus conspicuously marked and banded. All these examples, of larger size, of longer tails or other appendages, and of more conspicuous colouring, are probably indications of a less severe struggle for existence in these islands than in the larger tract of New Guinea, with a more abundant and more varied fauna; and this may apply even to the smaller islands, as compared with the larger in the immediate vicinity. The limited number of forms in the small islands compared with a similar area in the parent land, implies, perhaps, less competition and less danger; and thus allows, where all other conditions are favourable, an unchecked and continuous {422}development in size, form, and colour, until they become positively injurious. This law may not improbably apply to the New Guinea fauna itself, as compared with that of Borneo or any other similar country; and some of its peculiarities (such as its wonderful paradise-birds) may be due to long isolation, and consequent freedom from the influence of any competing forms. The difference between the very sober colours of the Coleoptera, and in a less degree of the birds, of Borneo, as compared with their brilliancy in New Guinea, always struck me most forcibly, and was long without any, even conjectural, explanation. It is not the place here to go further into this most curious and interesting subject. The reader who wishes for additional facts to aid him in forming an opinion, should consult Mr. Darwin's _Descent of Man_, chapters x. to xv.; and my own _Contributions to the Theory of Natural Selection_, chapters iii. and iv. _Timor Group._--_Mammalia._--In the group of islands between Java and Australia, from Lombok to Timor inclusive, we find a set of mammals similar to those of the Moluccas, but some of them different species. A wide-spread species of _Cuscus_ represents the Papuan element. A _Sorex_ and a peculiar species of wild pig, we may also accept as indigenous. Three others have almost certainly been introduced. These are, (1.) _Macacus cynomolgus_, the very commonest Malay monkey, which may have crossed the narrow straits from island to island between Java and Timor, though it seems much more probable that it was introduced by Malays, who constantly capture and rear the young of this species. (2.) _Cervus timoriensis_, a deer, said to be a distinct species, inhabits Timor, but it is probably only a variety of the _Cervus hippelaphus_ of Java. This animal is, however, much more likely to have crossed the sea than the monkey. (3.) _Paradoxurus fasciatus_, takes the place of _Viverra tangalunga_ in the Moluccas, both common and wide-spread civets which are often kept in confinement by the Malays. The _Felis megalotis_, long supposed to be a native of Timor, has been ascertained by Mr. Elliot to belong to a different country altogether. _Birds._--The birds are much more interesting, since they are {423}sufficiently numerous to allow us to determine their relations, and trace their origin, with unusual precision. There are 96 genera and 160 species of land-birds known to inhabit this group of islands; and on a careful analysis, they are found to be almost equally related to the Australian and Oriental regions, 30 genera being distinctly traceable to the former, and the same number to the latter. Their connection with the Moluccas is shown by the presence of the genera _Mimeta_, _Geoffroyus_, _Cacatua_, _Ptilopus_, and _Ianthænas_, together with _Megapodius_ and _Cerchneis_ represented by Moluccan species. _Turacoena_ shows a connection with Celebes, and _Scops_ is represented by a Celebesian species. The connection with Australia is shown by the genera _Sphæcothera_, _Gerygone_, _Myiagra_, _Pardalotus_, _Gliciphila_, _Amadina_, and _Aprosmictus_; while _Milvus_, _Hypotriorchis_, _Eudynamis_, and _Eurystomus_, are represented by Australian species. Other genera confined to or characteristic of the Australian region, are _Rhipidura_, _Monarcha_, _Artamus_, _Campephaga_, _Pachycephala_, _Philemon_, _Ptilotis_, and _Myzomela_. We now come to the Indo-Malay or Javan element represented by the following genera: 1. Turdus (T.) 2. Geocichla (T.) 3. Zoothera. 4. Megalurus (T.) 5. Orthotomus. 6. Pratincola (T.) 7. Oreicola (T.) 8. Drymocataphus (T.) 9. Parus. 10. Pycnonotus. 11. Oriolus. 12. Pericrocotus. 13. Cyornis (T.) 14. Hypothymis. 15. Tchitrea. 16. Lanius (T.) 17. Anthreptes. 18. Eulabes. 19. Estrilda (T.) 20. Erythrura (T.) 21. Yungipicus. 22. Merops. 23. Pelargopsis. 24. Ceyx. 25. Loriculus. 26. Treron (T.) 27. Iotreron (s.g. of _Ptilopus_). 28. Chalcophaps (T.) 29. Gallus (T.) 30. Strix. Such genera as _Merops_ and _Strix_, which are as much Australian as Oriental, are inserted here because they are represented by Javan species. The list is considerably swelled by genera which have reached Lombok across the narrow strait from Baly, but have passed no further. Such are _Zoothera_, _Orthotomus_, _Pycnonotus_, _Pericrocotus_ and _Strix_. A much larger number (12) stop short at Flores, leaving only 13, indicated in the list by (T) after their names, which reach Timor. It is evident, therefore, that these islands have been stocked from three chief sources,--the {424}Moluccas (with New Guinea and Celebes,) Australia, and Java. The Moluccan forms may well have arrived as stragglers from island to island, aided by whatever facilities have been afforded by lands now submerged. Most of the remainder have been derived either from Australia or from Java; and as their relations to these islands are very interesting, they must be discussed with some detail. _Origin of the Timorese Fauna._--We must first note, that 80 species, or exactly one-half of the land-birds of the islands, are peculiar and mostly very distinct, intimating that the immigration commenced long enough back to allow of much specific modification. There is also one peculiar genus of kingfishers, _Caridonax_, found only in Lombok and Flores, and more allied to Australian than to Oriental types. The fine white-banded pigeons (s. g. _Leucotreron_) are also almost peculiar; one other less typical species only being known, a native of N. Celebes. In order to compare the species with regard to their origin, we must first take away those of wide distribution from which no special indications can be obtained. In this case 49 of the land-birds must be deducted, leaving 111 species which afford good materials for comparison. These, when traced to their origin, show that 62 came from some part of the Australian region, 49 from Java or the Oriental region. But if we divide them into two groups, the one containing the species identical with those of the Australian or Oriental regions, the other containing _allied_ or _representative_ species peculiar to the islands, we have the following result: Species common to the Timorese Islands and the Oriental Region 30 Peculiar Timorese species allied to those of the Oriental Region 19 -- Total 49 Species common to the Timorese Islands and the Australian Region 18 Peculiar Timorese species allied to those of the Australian Region 44 -- Total 62 This table is very important, as indicating that the connection {425}with Australia was probably earlier than that with Java; since the majority of the Australian species have become modified, while the majority of the Oriental species have remained unchanged. This is due, no doubt, in part to the continued immigration of fresh individuals from Java, after that from Australia, the Moluccas and New Guinea had almost wholly ceased. We must also notice the very small proportion of the genera, either of Australia or Java, that have found their way into these islands, many of the largest and most wide-spread groups in both countries being altogether absent. Taking these facts into consideration, it is pretty clear that there has been no close and long-continued approximation of these islands to any part of the Australian region; and it is also probable that they were fairly stocked with such Australian groups as they possess before the immigration from Java commenced, or a larger number of characteristic Oriental forms would have been able to have established themselves. On looking at our map, we find that a shallow submerged bank extends from Australia to within about twenty miles of the coast of Timor; and this is probably an indication that the two countries were once only so far apart. This would have allowed the purely Australian types to enter, as they are not numerous; there being about 6 Australian species, and 10 or 12 representatives of Australian species, in Timor. All the rest may have been derived from the Moluccas or New Guinea, being mostly wide-spread genera of the Australian region; and the extension of Papua in a south-west direction towards Java (which was suggested as a means of providing New Guinea with peculiar Indo-Malay types not found in any other part of the region) may have probably served to supply Timor and Flores with the mass of their Austro-Malayan genera across a narrow strait or arm of the sea. Lombok, Baly, and Sumbawa were probably not then in existence, or nothing more than small volcanic cones rising out of the sea, thus leaving a distance of 300 miles between Flores and Java. Subsequently they grew into islands, which offered an easy passage for a number of Indo-Malay genera into such scantily stocked territories as Flores and Timor. The {426}north coast of Australia then sank, cutting off the supply from that country; and this left the Timorese group in the position it now occupies. The reptiles and fishes of this group are too little known to enable us to make any useful comparison. _Insects._--The insects, though not numerous, present many fine species, some quite unlike any others in the Archipelago. Such are--_Papilio liris_, _Pieris læta_, _Cirrochroa lamarckii_ and _C. leschenaultii_ among butterflies. The Coleoptera are comparatively little known, but in the insects generally the Indo-Malay element predominates. This may have arisen from the peculiar vegetation and arid climate not being suitable to the Papuan insects. Why Australian forms did not establish themselves we cannot conjecture; but the field appears to have been open to immigrants from Java, the climate and vegetation of which island at its eastern extremity approximates to that of the Timorese group. The insects are, however, so peculiarly modified as to imply a very great antiquity, and this is also indicated by a group of Sylviine birds here classed under _Oreicola_, but some of which probably form distinct genera. There may, perhaps, have been an earlier and a later approximation to Java, which, with the other changes indicated, would account for most of the facts presented by the fauna of these islands. One deduction is, at all events, clear: the extreme paucity of indigenous mammals along with the absence of so many groups of birds, renders it certain that the Timorese islands did not derive their animal life by means of an actual union with any of the large islands either of the Australian or the Oriental regions. _Celebes Group._--We now come to the Island of Celebes, in many respects the most remarkable and interesting in the whole region, or perhaps on the globe, since no other island seems to present so many curious problems for solution. We shall therefore give a somewhat full account of its peculiar fauna, and endeavour to elucidate some of the causes to which its zoological isolation may be attributed. _Mammalia._--The following is the list of the mammalia of {427}Celebes as far as at present known, though many small species may yet be discovered. 1. Cynopithecus nigrescens. 2. Tarsius spectrum. 3. Viverra tangalunga. 4. Cervus hippelaphus. 5. Anoa depressicornis. 6. Sus celebensis. 7. Barbirusa alfurus. 8. Sciurus (5 peculiar sp.) 9. Mus (2 peculiar sp.) 10. Cuscus (2 peculiar sp.) Also 7 species of bats, of which 5 are peculiar. The first--a large black ape--is itself an anomaly, since it is not closely allied to any other form of quadrumana. Its flat projecting muzzle, large superciliary crests and maxillary ridges, with the form and appearance of its teeth, separate it altogether from the genus _Macacus_, as represented in the Indo-Malay islands, and ally it closely to the baboons of Africa.[15] We have already seen reason to suppose that it has been carried to Batchian, and there is some doubt about the allied species or variety (_C. niger_) of the Philippines being really indigenous there; in which case this interesting form will remain absolutely confined to Celebes. (2.) The tarsier is a truly Malayan species, but it is said to occur in a small island at the northern extremity of Celebes and on some of the Philippine Islands. It might possibly have been introduced there. (3) and (4)--a civet and a deer--are, almost certainly, as in the Moluccas, introduced species. (5.) _Anoa depressicornis._ This is one of the peculiar Celebesian types; a small straight-horned wild-bull, anatomically allied to the buffaloes, and somewhat resembling the bovine antelopes of Africa, but having no near allies in the Oriental region. (6.) _Sus Celebensis_; a peculiar species of wild-pig. (7.) _Babirusa alfurus_; another remarkable type, having no near allies. It differs in its dentition from the typical Suidæ, and seems to approach the African Phacochoeridæ, The manner in which the canines of the upper jaw are reversed, and grow directly upwards in a spiral curve over the eyes, is unique among mammalia. (8.) Five squirrels inhabit Celebes, and all are peculiar species. (9.) These are forest rats of the sub-genus _Gymnomys_, allied to Australian species. 10. _Cuscus._ This typical {428}Australian form is represented in Celebes by two peculiar species. Leaving out the Indo-Malay _species_, which may probably have been introduced by man, and are at all events comparatively recent immigrants, and the wild pig, a genus which ranges over the whole archipelago and which has therefore little significance, we find two genera which have come from the Australian side,--_Cuscus_ and _Mus_; and four from the Oriental side,--_Cynopithecus_, _Anoa_, _Babirusa_, and _Sciurus_. But _Sciurus_ alone corresponds to _Cuscus_, as a genus still inhabiting the adjacent islands; the other three being not only peculiar to Celebes, but incapable of being affiliated to any specially Oriental group. We seem, then, to have indications of two distinct periods; one very ancient, when the ancestors of the three peculiar genera roamed over some unknown continent of which Celebes formed, perhaps, an outlying portion;--another more recent, when from one side there entered _Sciurus_, and from the other _Cuscus_. But we must remember that the Moluccas to the east, possess scarcely any indigenous mammals except _Cuscus_; whereas Borneo and Java on the west, have nearly 50 distinct genera. It is evident then, that the facilities for immigration must have been much less with the Oriental than with the Australian region, and we may be pretty certain that at this later period there was no land connection with the Indo-Malay islands, or some other animals than squirrels would certainly have entered. Let us now see what light is thrown upon the subject by the birds. _Birds._--The total number of birds known to inhabit Celebes is 205, belonging to about 150 genera. We may leave out of consideration the wading and aquatic birds, most of which are wide-ranging species. There remain 123 genera and 152 species of land-birds, of which 9 genera and 66 species are absolutely confined to the island, while 20 more are found also in the Sula or Sanguir Islands, so that we may take 86 to be the number of peculiar Celebes species. Lord Walden, from whose excellent paper on the birds of Celebes (_Trans. Zool. Soc._ vol. viii. p. 23) most of these figures are obtained, estimates, that of the species which are not peculiar to Celebes, 55 are of Oriental and 22 of {429}Australian origin, the remainder being common to both regions. This shows a preponderant recent immigration from the West and North, which is not to be wondered at when we look at the long coast line of Java, Borneo, and the Philippine islands, with an abundant and varied bird population, on the one side, and the small scattered islands of the Moluccas, with a comparatively scanty bird-fauna, on the other. But, adopting the method here usually followed, let us look at the relations of the _genera_ found in Celebes, omitting for the present those which are peculiar to it. I divide these genera into two series:--those which are found in Borneo or Java but not in the Moluccas, and those which inhabit the Moluccas and not Borneo or Java; these being the respective sources from which, _primâ facie_, the species of these genera must have been derived. Genera which range widely into both these districts are rejected, as teaching us nothing of the origin of the Celebesian fauna. In a few cases, sub-genera which show a decided eastern or western origin, are given. GENERA DERIVED FROM BORNEO AND JAVA. 1. Geocichla. 2. Pratincola (sp.) 3. Trichastoma. 4. Oriolus (sp.) 5. Cyornis. 6. Hypothymis. 7. Hylocharis. 8. Æthopyga. 9. Nectarophila. 10. Anthreptes (sp.) 11. Munia (sp.) 12. Acridotheres. 13. Yungipicus. 14. Mulleripicus. 15. Rhamphococcyx. 16. Hierococcyx. 17. Hydrocissa. 18. Cranorrhinus. 19. Lyncornis. 20. Treron (sp.) 21. Gallus (sp.) 22. Spilornis. 23. Butastur. 24. Pernis. GENERA DERIVED FROM THE MOLUCCAS OR TIMOR. 1. Graucalus (sp.) 2. Chalcostetha. 3. Myzomela. 4. Munia (sp.) 5. Cacatua (sp.) 6. Tanygnathus. 7. Trichoglossus. 8. Scythrops (sp.) 9. Turacoena. 10. Reinwardtoenas (sp.) 11. Myristicivora (s. g.) 12. Ducula (s. g.) 13. Zonoenas (s. g.) 14. Lamproteron (s. g.) 15. Megapodius. These tables show a decided preponderance of Oriental over Australian forms. But we must remember that the immediately adjacent lands from whence the supply was derived, is {430}very much richer in the one case than in the other. The 24 genera derived from Borneo and Java are only about _one fourth_ of the characteristic genera of those islands; while the 15 Moluccan and Timorese genera are fully _one third_ of their characteristic types. The _proportion_ derived from the Australian, is greater than that derived from the Oriental side. We shall exhibit this perhaps more clearly, by giving a list of the important groups of each set of islands which are absent from Celebes. Important Families of Java and Borneo absent from Celebes. 1. Eurylæmidæ. 2. Timaliidæ. 3. Phyllornithidæ. 4. Pycnonotidæ 5. Laniidæ. 6. Megalæmidæ. 7. Trogonidæ. 8. Phasianidæ. Important Families of the Moluccas absent from Celebes. 1. Meliphagidæ. Additional important genera of Java or Borneo absent from Celebes. 1. Orthotomus. 2. Copsychus. 3. Enicurus. 4. Tchitrea. 5. Pericrocotus. 6. Irena. 7. Platylophus. 8. Dendrocitta. 9. Eulabes. 10. Hemicercus. 11. Chrysocolaptes. 12. Tiga. 13. Micropternus. 14. Batrachostomus. 15. Palæornis. 16. Rollulus. Important genera of the Moluccas absent from Celebes. 1. Mimeta. 2. Monarcha. 3. Rhipidura. 4. Pachycephala. 5. Lycocorax. 6. Alcyone. 7. Tanysiptera. 8. Geoffroyus. 9. Eclectus. 10. Platycercus. 11. Eos. 12. Lorius. If we reckon the absent families to be each represented by only two important genera, we shall find the deficiency on the Oriental side much the greatest; yet those on the side of the Moluccas are sufficiently remarkable. The Meliphagidæ are not indeed absolutely wanting, since a _Myzomela_ has now been found in Celebes; but all its larger and more powerful forms which range over almost the entire region, are absent. This may be balanced by the absence of the excessively abundant Timaliidæ of the Indo-Malay islands, which are represented by {431}only a single species; and by the powerful Phasianidæ, represented only by the common Malay jungle fowl, perhaps introduced. The entire absence of Pycnonotidæ is a very anomalous fact, since one of the largest genera, _Criniger_, is well represented in several islands of the Moluccas, and one has even been found in the Togian islands in the great northern inlet of Celebes; but yet it passes over Celebes itself. _Ceyx_, a genus of small kingfishers, is a parallel case, since it is found everywhere from India to New Guinea, leaving out only Celebes; but this comes among those curiosities of the Celebesian fauna which we shall notice further on. In the list of genera derived from Borneo or Java, no less than 6 are represented by identical species (indicated by sp. after the name); while in the Moluccan list 5 are thus identical. These must be taken to indicate, either that the genus is a recent introduction, or that stragglers still occasionally enter, crossing the breed, and thus preventing specific modification. In either case they depend on the existing state of things, and throw no light on the different distribution of land and sea which aided or checked migration in former times; and they therefore to some extent diminish the weight of the Indo-Malay affinity, as measured by the relations of the peculiar species of Celebes. From our examination of the evidence thus far,--that is, taking account firstly, of the _species_, and, secondly, of the _genera_, which are common to Celebes and the groups of islands between which it is situated, we must admit that the connexion seems rather with the Oriental than with the Australian region; but when we take into account the _proportion_ of the genera and species present, to those which are absent, and giving some weight to the greater extent of coast line on the Indo-Malay side, we seem justified in stating that the Austro-Malay element is rather the most fully represented. This result applies both to birds and mammals; and it leads us to the belief, that during the epoch of existing species and genera, Celebes has never been united with any extensive tract of land either on the Indo-Malay or Austro-Malay side, but has received immigrants from both during a very long period, the facilities for immigration having been rather the {432}greatest on the Austro-Malay or Australian side. We have now to consider what further light can be thrown on the subject by the consideration of the _peculiar genera_ of Celebes, and of those curiosities or anomalies of distribution to which we have referred. Nine genera of birds are altogether peculiar to Celebes; three more are found only in one other island, and seem to be typically Celebesian; while one is found in the Sula islands (which belongs to the Celebes group) and probably exists in Celebes also. The following is a list of these 13 genera: 1. _Artamides_ (Campephagidæ) 2. _Streptocitta_ (Corvidæ) 3. _Charitornis_ " 4. _Gazzola_, (s. g.) " 5. _Basilornis_ (Sturnidæ) 6. _Enodes_ " 7. _Scissirostrum_ " 8. _Monachalcyon_ (Alcedinidæ) 9. _Cittura_ " 10. _Ceycopsis_ " 11. _Meropogon_ (Meropidæ) 12. _Prioniturus_ (Psittacidæ) 13. _Megacephalon_ (Megapodiidæ) Of the above, _Artamides_, _Monachalcyon_, _Cittura_, and _Megacephalon_, are modifications of types characteristic of the Australian region. All are peculiar to Celebes except _Cittura_, found also in the Sanguir islands to the northward, but which seems to belong to the Moluccan group. _Streptocitta_, _Charitornis_, and _Gazzola_, are peculiar types of Corvidæ; the two former allied to the magpies, the latter to the jackdaws. _Charitornis_ is known only from the Sula islands east of Celebes, and is closely related to _Streptocitta_. There is nothing comparable to these three groups in any of the Malay islands, and they seem to have relations rather with the Corvidæ of the old-world northern continent. _Basilornis_, _Enodes_, and _Scissirostrum_, are remarkable forms of Sturnidæ. _Basilornis_ has a beautiful compressed crest, which in the allied species found in Ceram is elongated behind. _Enodes_ has remarkable red superciliary streaks, but seems allied to _Calornis_. _Scissirostrum_ seems also allied to _Calornis_ in general structure, but has a very peculiarly formed bill and nostrils. We can hardly say whether these three forms show more affinity to Oriental or to Australian types, but they add to the weight of evidence as to the great antiquity and isolation of the Celebesian fauna. _Scissirostrum_ has been classed with _Euryceros_, a {433}Madagascar bird, and with _Buphaga_, an African genus; but the peculiar beak and nostrils approximate more to _Cracticus_ and its allies, of the Australian region, which should probably form a distinct family. _Ceycopsis_ is undoubtedly intermediate between the Malayan _Ceyx_ and the African _Ispidina_, and is therefore especially interesting. _Meropogon_ is a remarkable form of bee-eater, allied to the Indo-Malayan _Nyctiornis_. _Prioniturus_ (the raquet-tailed parrots) of which two species inhabit Celebes, and one the Philippines, appears to be allied to the Austro-Malayan _Geoffroyus_. We must finally notice a few genera found in Celebes, whose nearest allies are not in the surrounding islands, and which thus afford illustrations of discontinuous distribution. The most remarkable, perhaps, is _Coracias_, of which a fine species inhabits Celebes; while the genus is quite unknown in the Indo-Malay sub-region, and does not appear again till we reach Burmah and India; and the species has no closer affinity for Indian than for African forms. _Myialestes_, a small yellow flycatcher, is another exmple; its nearest ally (_M. cinereocapilla_) being a common Indian bird, but unknown in the Malay islands. The Celebesian bird described by me as _Prionochilus aureolimbatus_, is probably a third case of discontinuous distribution, if (as a more careful examination seems to show) it is not a _Prionochilus_, but congeneric with _Pachyglossa_, a bird only found in the Himalayas. The fine pigeon, _Carpophaga forsteni_, belongs to a group found in the Philippines, Australia, and New Zealand; but the Celebes species is very distinct from all the others, and seems, if anything, more allied to that of New Zealand. The Sula islands (Sula-mangola, Sula-taliabo, and Sula-besi) lie midway between Celebes and the Moluccas, being 80 miles from the nearest part of Celebes, with several intervening islands, and 40 miles from Bouru, all open sea. Their birds show, as might be expected, a blending of the two faunas, but with a decided preponderance of that of Celebes. Out of 43 land birds which have been collected in these islands, we may deduct 6 as of wide range and no significance. Of the 37 remaining, 21 are Celebesian species, and 4 are new species but {434}allied to those of Celebes; while there are 10 Moluccan species and 2 new species allied to those of the Moluccas. It is curious that no less than 3 Moluccan genera, quite unknown in Celebes itself, occur here,--_Monarcha_, _Pachycephala_, and _Criniger_; but all these, as well as several other of the Moluccan birds, are rather weak flyers, and such as are likely to have been carried across by strong winds. Of the _genera_, 23 are from Celebes, 10 from the Moluccas. These facts show, that the Sula islands form part of the Celebes group, although they have received an infusion of Moluccan forms, which will perhaps in time spread to the main island, and diminish the remarkable individuality that now characterises its fauna. _Insects._--Of the reptiles and fishes of Celebes we have not sufficient information to draw any satisfactory conclusions. I therefore pass to the insects of which something more is known. The Butterflies of Celebes are not very numerous, less than 200 species in all having been collected; but a very large proportion of them, probably three-fourths of the whole, are peculiar. There is only one peculiar genus, _Amechania_, allied to _Zethera_ (a group confined to the Philippine Islands), with which it should perhaps be united. Most of the genera are of wide distribution in the archipelago, or are especially Malayan, only two truly Australian genera, _Elodina_ and _Acropthalmia_, reaching Celebes. On the other hand, 7 peculiar Oriental genera are found in Celebes, but not further east, viz., _Clerome_, _Adolias_, _Euripus_, _Apatura_, _Limenitis_, _Iolaus_, and _Leptocircus_. There are also several indications of a direct affinity with the continent rather than with Malaya, as in the cases already enumerated among birds. A fine butterfly, yet unnamed, almost exactly resembles _Dichorragia nesimachus_, a Himalayan species. _Euripus robustus_ is closely allied to _E. halitherses_ of N. India; there are no less than 5 species of _Limenitis_, all quite unlike those found in other parts of the archipelago. The butterflies of Celebes are remarkably distinguished from all others in the East, by peculiarities of form, size, and colour, which run through groups of species belonging to different genera. Many Papilionidæ and Pieridæ, and some {435}Nymphalidæ, have the anterior wings elongated, with the apex often acute, and, what is especially remarkable, an abrupt bend or shoulder near the base of the wing. (See _Malay Archipelago_, 3rd Ed. p. 281, woodcut.) No less than 13 species of _Papilio_, 10 Pieridæ, and 4 or 5 Nymphalidæ, are thus distinguished from their nearest allies in the surrounding islands or in India. In size again, a large number of Celebesian butterflies stand preeminent over their allies. The fine Papilios--_adamantius_, _blumei_, and _gigon_--are perfect giants by the side of the closely-allied forms of Java; while _P. androcles_ is the largest and longest-tailed, of all the true swallow-tailed group of the Old World. Among Nymphalidæ, the species of _Rhinopalpa_ and _Euripus_, peculiar to Celebes, are immensely larger than their nearest allies; and several of the Pieridæ are also decidedly larger, though in a less marked degree. In colour, many of the Celebesian butterflies differ from the nearest allied species; so that they acquire a singularity of aspect which marks them off from the rest of the group. The most curious case is that of three butterflies, belonging to three distinct genera (_Cethosia myrina_, _Messaras mæonides_, and _Atella celebensis_) all having a delicate violet or lilac gloss in lines or patches, which is wholly wanting in every allied species of the surrounding islands. These numerous peculiarities of Celebesian butterflies are very extraordinary; and imply isolation from surrounding lands, almost as much as do the strange forms of mammals and birds, which more prominently characterise this interesting island. Of the Coleoptera we know much less, but a few interesting facts may be noted. There are a number of fine species of _Cicindela_, some of peculiar forms; and one _Odontochila_, a South American genus; while _Collyris_ reaches Celebes from the Oriental region. In Carabidæ it has one peculiar genus, _Dicraspeda_; and a species of the fine Australian genus _Catadromus_. In Lucanidæ it has the Oriental genus, _Odontolabris_. In Cetoniidæ it has a peculiar genus, _Sternoplus_, and several fine _Cetoniæ_; but the characteristic Malayan genus, _Lomaptera_, found in every other island of the archipelago from Sumatra to New Guinea, is absent--an analogous fact to the case of _Ceyx_ among birds. {436}In Buprestidæ, the principal Austro-Malay genus, _Sambus_, is found here; while _Sponsor_, a genus 8 species of which inhabit Mauritius, has one species here and one in New Guinea. In Longicorns there are four peculiar genera, _Comusia_, _Pytholia_, _Bityle_, and _Ombrosaga_; but the most important features are the occurrence of the otherwise purely Indo-Malayan genera _Agelasta_, _Nyctimene_, and _Astathes_; and of the purely Austro-Malayan _Arrhenotus_, _Trysimia_, _Xenolea_, _Amblymora_, _Diallus_, and _Ægocidnus_. The remaining genera range over both portions of the archipelago. In the extensive family of Curculionidæ we can only notice the elegant genus, _Celebia_, allied to _Eupholus_, which, owing to its abundance and beauty, is a conspicuous feature in the entomology of the island. _Origin of the fauna of Celebes._--We have now to consider, briefly, what past changes of physical geography are indicated by the curious assemblage of facts here adduced. We have evidently, in Celebes, a remnant of an exceedingly ancient land, which has undergone many and varied revolutions; and the stock of ancient forms which it contains must be taken account of, when we speculate on the causes that have so curiously limited more recent immigrations. Going back to the arrival of those genera which are represented in Celebes by peculiar species, and taking first the Austro-Malay genera, we find among them such groups as _Zonoenas_ (s.g.), _Phlogoenas_, _Leucotreron_ (s.g.), and _Turacoena_, which are not found in the Moluccas at all; and _Myzomela_, found in Timor and Banda, but not in Ceram or Bouru, which are nearest to Celebes. This, combined with the curious absence of so many of the commonest Moluccan genera, leads to the conclusion that the Austro-Malay immigration took place by way of Timor and the southern part of New Guinea. It will be remembered, that to account for the Indo-Malayan forms in New Guinea, we suggested an extension of that country in a westerly direction just north of Timor. Now this is exactly what we require, to account for the stocking of Celebes with the Australian forms it possesses. At this time Borneo did not approach so near, and it was at a somewhat later period that the last great Indo-Malay migration set in; but {437}finding the country already fairly stocked, comparatively few groups were able to establish themselves. Going back a little farther, we come to the entrance of those few birds and insects which belong to India or Indo-China; and this probably occurred at the same time as that continental extension southward, which we found was required to account for a similar phenomenon in Java. Celebes, being more remote, received only a few stragglers. We have now to go much farther back, to the time when the ancestors of the peculiar Celebesian genera entered the country, and here our conjectures must necessarily be less defined. On the Australian side we have to account for _Megacephalon_, and the other genera of purely Papuan type. It may perhaps be sufficient to say, that we do not yet know that these genera, or some very close allies, do not still exist in New Guinea; in which case they may well have entered at the same time with the species, already referred to. If, on the other hand, they are really as isolated as they appear to be, they represent an earlier communication, either by an approximation of the two islands over the space now occupied by the Moluccas; or, what is perhaps more probable, through a former extension of the Moluccas, which have since undergone so much subsidence, as to lead to the extinction of a large proportion of their ancient fauna. The wide-spread volcanic action, and especially the prevalence of raised coral-reefs in almost all the islands, render this last supposition very probable. On the Oriental side the difficulty is greater; for here we find, what seem to be clear indications of a connection with Africa, as well as with Continental Asia, at some immensely remote epoch. _Cynopithecus_, _Babirusa_, and _Anoa_; _Ceycopsis_, _Streptocitta_, and _Gazzola_ (s. g.), and perhaps _Scissirostrum_, may be well explained as descendants of ancestral types in their respective groups, which also gave rise to the special forms of Africa on the one hand, and of Asia on the other. For this immigration we must suppose, that at a period before the formation of the present Indo-Malay Islands, a great tract of land extended in a north-westerly direction, till it met the old Asiatic continent. This may have been before {438}the Himalayas had risen to any great height, and when a large part of what are now the cold plateaus of Central Asia may have teemed with life, some forms of which are preserved in Africa, some in Malaya, and a few in Celebes. Here may have lived the common ancestor of _Sus_, _Babirusa_, and _Phacochoerus_; as well as of _Cynopithecus_, _Cynocephalus_, and _Macacus_; of _Anoa_ and _Bubalus_; of _Scissirostrum_ and _Euryceros_; of _Ceyx_, _Ceycopsis_, and _Ispidina_. Such an origin accounts, too, for the presence of the North-Indian forms in Celebes; and it offers less difficulties than a direct connection with continental Africa, which once appeared to be the only solution of the problem. If this south-eastward extension of Asia occurred at the same time as the north-eastward extension of South Africa and Madagascar, the two early continents may have approached each other sufficiently to have allowed of some interchange of forms: _Tarsius_ may be the descendant of some Lemurine animal that then entered the Malayan area, while the progenitors of _Cryptoprocta_ may then have passed from Asia to Madagascar. It is true that we here reach the extremest limits of speculation; but when we have before us such singular phenomena as are presented by the fauna of the island of Celebes, we can hardly help endeavouring to picture to our imaginations by what past changes of land and sea (in themselves not improbable) the actual condition of things may have been brought about. _II. Australia and Tasmania, or the Australian Sub-region._ A general sketch of Australian zoology having been given in the earlier part of this chapter, it will not be necessary to occupy much time on this sub-region, which is as remarkably homogeneous as the one we have just left is heterogeneous. Although much of the northern part of Australia is within the tropics, while Victoria and Tasmania are situated from 36° to 43° south latitude, there is no striking change in the character of the fauna throughout the continent; a number of important genera extending over the whole country, and giving a very uniform character to its zoology. The eastern parts, including the colonies of New South Wales and Queensland, are undoubtedly the richest, several peculiar types being found only here. The southern portion is somewhat poorer, and has very few peculiar forms; and Tasmania being isolated is poorer still, yet its zoology has much resemblance to that of Victoria, from which country it has evidently not been very long separated. The north, as far as yet known, is characterised by hardly any peculiar forms, but by the occurrence of a number of Papuan types, which have evidently been derived from New Guinea. Plate XI. [Illustration] A SCENE IN TASMANIA, WITH CHARACTERISTIC MAMMALIA. {439}_Mammalia._--The Australian sub-region contains about 160 species of Mammalia, of which 3 are Monotremata, 102 Marsupials, 23 Chiroptera, 1 Carnivora (the native dog, probably not indigenous), and 31 Muridæ. The north is characterised by a species of the Austro-Malayan genus _Cuscus_. _Phascolarctos_ (the koala, or native bear) is found only in the eastern districts; _Phascolomys_ (the wombat) in the south-east and Tasmania; _Petaurista_ (a peculiar form of flying opossum) in the east. _Thylacinus_ (the zebra-wolf), and _Sarcophilus_ (the "native devil"), two carnivorous marsupials, are confined to Tasmania. West Australia, the most isolated and peculiar region botanically, alone possesses the curious little honey-eating _Tarsipes_, and the _Peragalea_, or native rabbit. The remarkable _Myrmecobius_, a small ant-eating marsupial, is found in the west and south; and _Onychogalea_, a genus of kangaroos, in West and Central Australia. All the other genera have a wider distribution, as will be seen by a reference to the list at the end of this chapter. _Plate XI. A Scene in Tasmania, with Characteristic Mammalia._--As some of the most remarkable Mammalia of the Australian region are now found only in Tasmania, we have chosen this island for the scene of our first illustration of the fauna of the Australian sub-region. The pair of large striped animals are zebra-wolves (_Thylacinus cynocephalus_), the largest and most destructive of the carnivorous marsupials. These creatures used to be tolerably plentiful in Tasmania, where they are alone found. They are also called "native tigers," or "native hyænas;" and being destructive to sheep, they have been destroyed by the farmers and will doubtless soon be exterminated. In the foreground on {440}the left is a bandicoot (_Perameles gunnii_). These are delicate little animals allied to the kangaroos; and they are found in all parts of Australia, and Tasmania, to which latter country this species is confined. On the right is the wombat (_Phascolomys wombat_), a root-eating marsupial, with large incisor teeth like those of our rodents. They inhabit south-east Australia and Tasmania. In the foreground is the porcupine ant-eater (_Echidna setosa_), belonging to a distinct order of mammalia, Monotremata, of which the only other member is the duck-billed _Ornithorhynchus_. These animals are, however, more nearly allied to the marsupials, than to the insectivora or edentata of the rest of the world, which in some respects they resemble. An allied species (_Echidna hystrix_) inhabits south-east Australia. _Birds._--Australia (with Tasmania) possesses about 630 species of birds, of which 485 are land-birds. Not more than about one-twentieth of these are found elsewhere, so that it has a larger proportion of endemic species than any other sub-region on the globe. These birds are divided among the several orders as follows: Passeres 306 Picariæ 41 Psittaci 60 Columbæ 24 Gallinæ 15 Accipitres 36 Grallæ 77 Anseres 65 Struthiones 3 The Psittaci, we see, are very richly represented, while the Picariæ are comparatively few; and the Columbæ are scarce as compared with their abundance in the Austro-Malay sub-region. Birds seem to be very evenly distributed over all Australia; comparatively few genera of importance being locally restricted. In the eastern districts alone, we find _Origma_, and _Orthonyx_ (Sylviidæ); _Sericulus_ and _Ptilorhynchus_ (Paradiseidæ); _Leucosarcia_ (Columbidæ); and _Talegalla_ (Megapodiidæ). _Nectarinia_, _Pitta_, _Ptilorhis_, _Chlamydodera_, and _Sphecotheres_, range from the north down the east coasts. _Nanodes_ (Psittacidæ), and _Lipoa_ (Megapodiidæ), are southern forms, the first extending {441}to Tasmania; which island appears to possess no peculiar genus of birds except _Eudyptes_, one of the penguins. West Australia has no wholly peculiar genus except _Geopsittacus_, a curious form of ground parroquet; the singular _Atrichia_, first found here, having been discovered in the east. In North Australia, _Emblema_ (Ploceidæ) is the only peculiar Australian genus, but several Austro-Malayan and Papuan genera enter,--as, _Syma_ and _Tanysiptera_ (Alcedinidæ); _Machærihynchus_ (Muscicapidæ); _Calornis_ (Sturnidæ); _Manucodia_, _Ptilorhis_, and _Æluroedus_ (Paradiseidæ); _Megapodius_; and _Casuarius_. The presence of a species of bustard (_Eupodotis_) in Australia, is very curious, its nearest allies being in the plains of India and Africa. Among waders the genus _Tribonyx_, a thick-legged bird somewhat resembling the _Notornis_ of New Zealand, though not closely allied to it, is the most remarkable. The district where the typical Australian forms most abound is undoubtedly the eastern side of the island. The north and south are both somewhat poorer, the west much poorer, although it possesses a few very peculiar forms, especially among Mammalia. Tasmania is the poorest of all, a considerable number of genera being here wanting; but, except the two peculiar carnivorous marsupials, it possesses nothing to mark it off zoologically from the adjacent parts of the main land. It is probable that its insular climate, more moist and less variable than that of Australia, may not be suitable to some of the absent forms; while others may require more space and more varied conditions, than are offered by a comparatively small island. The remaining classes of animals have been already discussed in our sketch of the region as a whole (p. 396). _Plate XII. Illustrating the Fauna of Australia._--In this plate we take New South Wales as our locality, and represent chiefly, the more remarkable Australian types of birds. The most conspicuous figure is the wonderful lyre-bird (_Menura superba_), the elegant plumage of whose tail is altogether unique in the whole class of birds. The unadorned bird is the female. In the centre is the emu (_Dromæus novæ-hollandiæ_), the representative in Australia, of the ostrich in Africa and America, but {442}belonging to a different family, the Casurariidæ. To the right are a pair of crested pigeons (_Ocyphaps lophotes_), one of the many singular forms of the pigeon family to which the Australian region gives birth. In every other part of the globe pigeons are smooth-headed birds, but here they have developed three distinct forms of crest, as seen in this bird, the crowned pigeon figured in Plate X., and the double-crested pigeon (_Lopholæmus antarcticus_). The large bird on the tree is one of the Australian frog-mouthed goat-suckers (_Podargus strigoides_), which are called in the colony "More-pork," from their peculiar cry. They do not capture their prey on the wing like true goat-suckers, but hunt about the branches of trees at dusk, for large insects, and also for unfledged birds. A large kangaroo (_Macropus giganteus_) is seen in the distance; and passing through the air, a flying opossum (_Petaurus sciureus_), a beautiful modification of a marsupial, so as to resemble in form and habits the flying squirrels of the northern hemisphere. _III. The Pacific Islands, or Polynesian Sub-region._ Although the area of this sub-region is so vast, and the number of islands it contains almost innumerable, there is a considerable amount of uniformity in its forms of animal life. From the Ladrone islands on the west, to the Marquesas on the east, a distance of more than 5,000 miles, the same characteristic genera of birds prevail; and this is the only class of animals on which we can depend, mammalia being quite absent, and reptiles very scarce. The Sandwich Islands, however, form an exception to this uniformity; and, as far as we yet know, they are so peculiar that they ought, perhaps, to form a separate sub-region. They are, however, geographically a part of Polynesia; and a more careful investigation of their natural history may show more points of agreement with the other islands. It is therefore a matter of convenience, at present, to keep them in the Polynesian sub-region, which may be divided into Polynesia proper and the Sandwich Islands. Plate XII. [Illustration] THE PLAINS OF NEW SOUTH WALES, WITH CHARACTERISTIC ANIMALS. {443}Polynesia proper consists of a number of groups of islands of some importance, and a host of smaller intermediate islets. For the purpose of zoological comparison, we may class them in four main divisions. 1. The Ladrone and Caroline Islands; 2. New Caledonia and the New Hebrides; 3. The Fiji, Tonga, and Samoa Islands; 4. The Society, and Marquesas Islands. The typical Polynesian fauna is most developed in the third division; and it will be well to describe this first, and then show how the other islands diverge from it, and approximate other sub-regions. _Fiji, Tonga, and Samoa Islands._--The land-birds inhabiting these islands belong to 41 genera, of which 17 are characteristic of the Australian region, and 9 more peculiarly Polynesian. The characteristic Australian genera are the following: _Petroica_ (Sylviidæ); _Lalage_ (Campephagidæ); _Monarcha_, _Myiagra_, _Rhipidura_ (Muscicapidæ); _Pachycephala_ (Pachycephalidæ); _Rectes_ (Laniidæ); _Myzomela_, _Ptilotis_, _Anthochæra_ (Meliphagidæ); _Amadina_, _Eythrura_, (Ploceidæ); _Artamus_ (Artamidæ); _Lorius_ (Trichoglossidæ); _Ptilopus_, _Phlogænas_ (Columbidæ); _Megapodius_ (Megapodiidæ). The peculiar Polynesian genera are:--_Tatare_, _Lamprolia_ (Sylviidæ); _Aplonis_, _Sturnodes_ (Sturnidæ); _Todiramphus_ (Alcedinidæ); _Pyrhulopsis_, _Cyanoramphus_, (Platycercidæ); _Coriphilus_ (Trichoglossidæ); _Didunculus_ (Didunculidæ). The wide-spread genera are _Turdus_, _Zosterops_, _Hirundo_, _Halcyon_, _Collocalia_, _Eudynamis_, _Cuculus_, _Ianthoenas_, _Carpophaga_, _Turtur_, _Haliæetus_, _Astur_, _Circus_, _Strix_, _Asio_. The aquatic birds are fifteen in number, all wide-spread species except one--a form of moor-hen (Gallinulidæ), which has been constituted a new genus _Pareudiastes_. _Society, and Marquesas Islands._--Here, the number of genera of land-birds has considerably diminished, amounting only to 16 in all. The characteristic Australian genera are 5;--_Monarcha_, _Anthochæra_, _Trichoglossus_, _Ptilopus_, and _Phlogoenas_. The Polynesian genera are 4;--_Tatare_, _Todiramphus_, _Cyanoramphus_, _Coriphilus_, and one recently described genus, _Serresius_, an extraordinary form of large fruit pigeon, here classed under _Carpophaga_. These remote groups have thus all the character of Oceanic islands, even as regards the rest of Polynesia, since they {444}possess hardly anything, but what they might have received by immigration over a wide extent of ocean. _Ladrone, and Caroline Islands._--These extensive groups of small islands are very imperfectly known, yet a considerable number of birds have been obtained. They possess two peculiar Polynesian genera, _Tatare_ and _Sturnodes_; one peculiar sub-genus, _Psammathia_ (here included under _Acrocephalus_); and ten of the typical Australian genera found in Polynesia,--_Lalage_, _Monarcha_, _Myiagra_, _Rhipidura_, _Myzomela_, _Erythrura_, _Artamus_, _Phlogoenas_, _Ptilopus_, and _Megapodius_, as well as the Papuan genus _Rectes_, and the Malayan _Calornis_;--so that they can be certainly placed in the sub-region. Genera which do not occur in the other Polynesian islands are, _Acrocephalus_, (s.g. _Psammathia_) originally derived perhaps from the Philippines; and _Caprimulgus_, a peculiar species, allied to one from Japan. _New Caledonia, and the New Hebrides._--Although these islands seem best placed with Polynesia, yet they form a transition to Australia proper, and to the Papuan group. They possess 30 genera of land-birds, 18 of which are typical of the Australian region; but while 13 are also Polynesian, there are 5 which do not pass further east. These are _Acanthiza_, _Eopsaltria_, _Gliciphila_, _Philemon_, and _Ianthoenas_. The peculiar Polynesian genus, _Aplonis_, of which three species inhabit New Caledonia, link it to the other portions of the sub-region. The following are the genera at present known from New Caledonia:--_Turdus_, _Acanthiza_, _Campephaga_, _Lalage_, _Myiagra_, _Rhipidura_, _Pachycephala_, _Eopsaltria_, _Corvus_, _Physocorax_ (s.g. of _Corvus_, allied to the jackdaws), _Glicphila_, _Anthochæra_, _Philemon_, _Zosterops_, _Erythrura_, _Aplonis_, _Artamus_, _Cuculus_, _Halcyon_, _Collocalia_, _Cyanoramphus_, _Trichoglossus_, _Ptilopus_, _Carpophaga_, _Macropygia_, _Ianthoenas_, _Chalcophaps_, _Haliastur_, _Accipiter_. The curious _Rhinochetus jubatus_, forming the type of a distinct family of birds (Rhinochetidæ), allied to the herons, is only known from New Caledonia. It thus appears, that not more than about 50 genera and 150 species of land-birds, are known from the vast number of islands that are scattered over the Central Pacific, and it is not probable {445}that the number will be very largely increased. Some of the species, as the _Eudynamis taitensis_ and _Tatare longirostris_, range over 40° of longitude, from the Fiji Islands to the Marquesas. In other genera, as _Cyanoramphus_ and _Ptilopus_, each important island or group of islands, has its peculiar species. The connection of all these islands with each other, on the one hand, and their close relation to the Australian region, on the other, are equally apparent; but we have no sufficient materials for speculating with any success, on the long series of changes that have brought about their existing condition, as regards their peculiar forms of animal life. _Sandwich Islands._--This somewhat extensive group of large islands, is only known to contain 11 genera and 18 species of indigenous land-birds; and even of this small number, two birds of prey are wide ranging species, which may well have reached the islands during their present isolated condition. These latter are, _Strix delicatula_, an owl spread over Australia and the Pacific; and _Asio accipitrinus_, a species which has reached the Galapagos from S. America, and thence perhaps the Sandwich Islands. Of the remaining 8 genera, one is a crow (_Corvus hawaiensis_), and another a fishing eagle (_Pandion solitarius_), of peculiar species; leaving 7 genera, which are all (according to Mr. Sclater) peculiar. First we have _Chasiempis_, a genus of Muscicapidæ, containing two species (which may however belong to distinct genera); and as the entire family is unknown on the American continent these birds must almost certainly be allied to some of the numerous Muscicapine forms of the Australian region. Next we have the purely Australian family Meliphagidæ, represented by two genera,--_Moho_, an isolated form, and _Chætoptila_, a genus established by Mr. Sclater for a bird before classed in _Entomyza_, an Australian group. The four remaining genera are believed by Mr. Sclater to belong to one group, the Drepanididæ, altogether confined to the Sandwich Islands. Two of them, _Drepanis_ and _Hemignathus_, with three species each, are undoubtedly allied; the other two, _Loxops_ and _Psittirostra_, have usually been classed as finches. The former seem to approach the Dicæidæ; and all resemble this group in their coloration, {446}The aquatic birds and waders all belong to wide-spread genera, and only one or two are peculiar species. The Sandwich Islands thus possess a larger proportion of peculiar genera and species of land-birds than any other group of islands, and they are even more strikingly characterised by what seems to be a peculiar family. The only other class of terrestrial animals at all adequately represented on these islands, are the land shells; and here too we find a peculiar family, sub-family, or genus (Achatinella or Achatinellidæ) consisting of a number of genera, or sub-genera,--according to the divergent views of modern conchologists,--and nearly 300 species. The Rev. J. T. Gulick, who has made a special study of these shells on the spot, considers that there are 10 genera, some of which are confined to single islands. The species are so restricted that their average range is not more than five or six square miles, while some are confined to a tract of only two square miles in extent, and very few range over an entire island. Some species are confined to the mountain ridges, others to the valleys; and each ridge or valley possesses its peculiar species. Considerably more than half the species occur in the island of Oahu, where there is a good deal of forest. Very few shells belonging to other groups occur, and they are all small and obscure; the Achatinellæ almost monopolising the entire archipelago. _Remarks on the probable past history of the Sandwich Islands._--The existence of these peculiar groups of birds and land-shells in so remote a group of volcanic islands, clearly indicates that they are but the relics of a more extensive land; and the reefs and islets that stretch for more than 1,000 miles in a west-north-west direction, may be the remains of a country once sufficiently extensive to develope these and many other, now extinct, forms of life.[16] Some light may perhaps be thrown on the past history of the {447}Sandwich Islands, by the peculiar plants which are found on their mountains. The peak of Teneriffe produces no Alpine plants of European type, and this has been considered to prove that it has been always isolated; whereas the occurrence of North Temperate forms on the mountains of Java, accords with other evidence of this island having once formed part of the Asiatic continent. Now on the higher summits of the Sandwich Islands, nearly 30 genera of Arctic and North Temperate flowering plants have been found. Many of these occur also in the South Temperate zone, in Australia or New Zealand; but there are others which seem plainly to point to a former connection with some North Temperate land, probably California, as a number of islets are scattered in the ocean between the two countries. The most interesting genera are the following:--_Silene_, which is wholly North Temperate, except that it occurs in S. Africa; _Vicia_, also North Temperate, and in South Temperate America; _Fragaria_, with a similar distribution; _Aster_, widely spread in America, otherwise North Temperate only; _Vaccinium_, wholly confined to the northern hemisphere, in cold and temperate climates. None of these are found in Australia or New Zealand; and their presence in the Sandwich Islands seems clearly to indicate a former approximation to North Temperate America, although the absence of any American forms of vertebrata renders it certain that no actual land connection ever took place. Recent soundings have shown, that the Sandwich Islands rise from a sea which is 3,000 fathoms or 18,000 feet deep; while there is a depth of at least 2,000 fathoms all across to California on one side, and to Japan on the other. Between the Fiji Islands, New Caledonia, the Solomon Islands, and Australia, the depth is about 1,300 fathoms, and between Sydney and New Zealand 2,600 fathoms; showing, in every case, a general accordance between the depth of sea and the approximation of the several faunas. In a few more years, when it is to be hoped we shall know the contour of the sea-bottom better than that of the continents, we shall be able to arrive at more definite and trustworthy conclusions as to the probable changes {448}of land and sea by which the phenomena of animal distribution in the Pacific have been brought about. _Reptiles of the Polynesian Sub-region._--The researches of Mr. Darwin on Coral Islands, proved, that large areas in the Pacific Ocean have been recently subsiding; but the peculiar forms of life which they present, no less clearly indicate the former existence of some extensive lands. The total absence of Mammalia, however, shows either that these lands never formed part of the Australian or Papuan continents, or if they did, that they have been since subjected to such an amount of subsidence as to exterminate most of their higher terrestrial forms of life. It is a remarkable circumstance, that although Mammalia (except bats) are wanting, there are a considerable number of reptiles ranging over the whole sub-region. Lizards are the most numerous, five families and fourteen genera being represented, as follows:-- 1. Cryptoblepharus (Gymnopthalmidæ ) Fiji Islands. 2. Ablepharus " All the islands. 3. Lygosoma (Scincidæ) Pelew Islands, New Caledonia. 4. Mabouya " Samoa Islands. 5. Euprepes " Pacific Islands. 6. _Dactyloperus_ (Geckotidæ) Sandwich Islands. 7. _Doryura_ (Geckotidæ) Pacific Islands. 8. Gehyra " Fiji Islands. 9. _Amydosaurus_ " Tahiti. 10. Heteronota " Fiji Islands. 11. _Correlophus_ " New Caledonia. 12. _Brachylophus_ (Iguanidæ) Fiji Islands. 13. Lophura (Agamidæ) Pelew Islands. 14. _Chloroscartes_ " Fiji Islands. The first five are wide-spread genera, represented mostly by peculiar species; but sometimes the species themselves have a wide range, as in the case of _Ablepharus poecilopleurus_, which (according to Dr. Günther) is found in Timor, Australia, New Caledonia, Savage Island (one of the Samoa group), and the Sandwich Islands! _Gehyra_ and _Heteronota_ are Australian genera; while _Lophura_ has reached the Pelew Islands from the Moluccas. The remainder (printed in italics), are peculiar genera; _Brachylophus_ being especially interesting as an example of an {449}otherwise peculiar American family, occurring so far across the Pacific. Snakes are much less abundant, only four genera being represented, one of them marine. They are, _Anoplodipsas_, a peculiar genus of Amblycephalidæ from New Caledonia; _Enygrus_, a genus of Pythonidæ from the Fiji Islands; _Ogmodon_, a peculiar genus of Elapidæ, also from the Fiji Islands, but ranging to Papua and the Moluccas; and _Platurus_, a wide-spread genus of sea-snakes (Hydrophidæ). In the more remote Sandwich and Society Islands there appear to be no snakes. This accords with our conclusion that lizards have some special means of dispersal over the ocean which detracts from their value as indicating zoo-geographical affinities; which is further proved by the marvellous range of a single species (referred to above) from Australia to the Sandwich Islands. A species of _Hyla_ is said to inhabit the New Hebrides, and several species of _Platymantis_ (tree-frogs) are found in the Fiji Islands; but otherwise the Amphibians appear to be unrepresented in the sub-region, though they will most likely be found in so large an island as New Caledonia. From the foregoing sketch, it appears, that although the reptiles present some special features, they agree on the whole with the birds, in showing, that the islands of Polynesia all belong to the Australian region, and that in the Fiji Islands is to be found the fullest development of their peculiar fauna. _IV. New Zealand Sub-region._ The islands of New Zealand are more completely oceanic than any other extensive tract of land, being about 1,200 miles from Australia and nearly the same distance from New Caledonia and the Friendly Isles. There are, however, several islets scattered around, whose productions show that they belong to the same sub-region;--the principal being, Norfolk Island, Lord Howe's Island, and the Kermadec Isles, on the north; Chatham Island on the east; the Auckland and Macquarie Isles on the south;--and if these were once joined to {450}New Zealand, there would have been formed an island-continent not much inferior in extent to Australia itself. New Zealand is wholly situated in the warmer portion of the Temperate zone, and enjoys an exceptionally mild and equable climate. It has abundant moisture, and thus comes within the limits of the South-Temperate forest zone; and this leads to its productions often resembling those of the tropical, but moist and wooded, islands of the Pacific, rather than those of the temperate, but arid and scantily wooded plains of Australia. The two islands of New Zealand are about the same extent (approximately) as the British Isles, but the difference in the general features of their natural history is very great. There are, in the former, no mammalia, less than half as many birds, very few reptiles and fresh-water fishes, and an excessive and most unintelligible poverty of insects; yet, considering the situation of the islands and their evidently long-continued isolation, the wonder rather is that their fauna is so varied and interesting as it is found to be. Our knowledge of this fauna, though no doubt far from complete, is sufficiently ample; and it will be well to give a pretty full account of it, in order to see what conclusions may be drawn as to its origin. _Mammalia._--The only mammals positively known as indigenous to New Zealand are two bats, both peculiar to it,--_Scotophilus tuberculatus_ and _Mystacina tuberculata_. The former is allied to Australian forms; the latter is more interesting, as being a peculiar genus of the family Noctilionidæ, which does not exist in Australia; and in having decided resemblances to the Phyllostomidæ of South America, so that it may almost be considered to be a connecting link between the two families. A forest rat is said to have once abounded on the islands, and to have been used for food by the natives; but there is much doubt as to what it really was, and whether it was not an introduced species. The seals are wide-spread antarctic forms which have no geographical significance. _Birds._--About 145 species of birds are natives of New Zealand, of which 88 are waders or aquatics, leaving 57 land-birds {451}belonging to 34 genera. Of this latter number, 16, or nearly half, are peculiar; and there are also 5 peculiar genera of waders and aquatic birds, making 21 in all. Of the remaining genera of land-birds, four are cosmopolite or of very wide range, while the remainder are characteristic of the Australian region. The following is a list of the Australian genera found in New Zealand: _Sphenæacus_, _Gerygone_, _Orthonyx_ (Sylviidæ); _Graucalus_ (Campephagidæ); _Rhipidura_ (Muscicapidæ); _Anthochæra_ (Meliphagidæ); _Zosterops_ (Dicæidæ); _Cyanoramphus_ (Platycercidæ); _Carpophaga_ (Columbidæ); _Hieracidea_ (Falconidæ); _Tribonyx_ (Rallidæ). Besides these there are several genera of wide range, as follows:--_Anthus_ (Motacillidæ); _Hirundo_ (Hirundinidæ); _Chrysococcyx_, _Eudynamis_ (Cuculidæ); _Halcyon_ (Alcedinidæ); _Coturnix_ (Tetraonidæ); _Circus_ (Falconidæ); _Athene_ (Strigidæ). Most of the above genera are represented by peculiar New Zealand species, but in several cases the species are identical with those of Australia, as in the following: _Anthochæra carunculata_, _Zosterops lateralis_, _Hirundo nigricans_, and _Chrysococcyx lucidus_; also one--_Eudynamis taitensis_--which is Polynesian. We now come to the genera peculiar to New Zealand, which are of especial interest: LIST OF GENERA OF BIRDS PECULIAR TO NEW ZEALAND. No. of Family and Genus. Species. Remarks. SYLVIIDÆ. 1. Myiomoira 3 Allied to Petroica, an Australian genus 2. Miro 2 " " " " TIMALIIDÆ (?) 3. Turnagra 2 Of doubtful affinities. SITTIDÆ. 4. Xenicus 3 Of doubtful affinities. 5. Acanthisitta 1 Of doubtful affinities. PARIDÆ. 6. Certhiparus 2 Of doubtful affinities. MELIPHAGIDÆ. 7. Prosthemadera 1 Peculiar genera of honeysuckers, a 8. Pogonornis 1 family which is confined to the 9. Anthornis 3 Australian Region. STURNIDÆ. {452} 10. Creadion 2 These three genera are probably 11. Heterolocha 1 allied, and perhaps form a distinct 12. Callæas 2 family. NESTORIDÆ. 13. Nestor 3 A peculiar family of Parrots. STRINGOPIDÆ. 14. Stringops 1 A peculiar family of Parrots. STRIGIDÆ. 15. (Sceloglaux) 1 s.g. of Athene. RALLIDÆ. 16. Ocydromus 6 Allied to _Eulabeornis_, an Australian genus. 17. Notornis 1 Allied to _Porphyrio_, a genus of wide range. CHARADRIIDÆ. 18. Thinornis 1 19. Anarhynchus 1 ANATIDÆ. 20. Hymenolæmus 1 Allied to _Malacorhynchus_, an Australian genus. APTERYGIDÆ. 21. Apteryx 4 Forming a peculiar family. We have thus a wonderful amount of speciality; yet the affinities of the fauna, whenever they can be traced, are with Australia or Polynesia. Nine genera of New Zealand birds are characteristically Australian, and the eight genera of wide range are Australian also. Of the peculiar genera, 7 or 8 are undoubtedly allied to Australian groups. There are also four Australian and one Polynesian _species_. Even the peculiar _family_, Nestoridæ is allied to the Australian Trichoglossidæ. We have therefore every gradation of similarity to the Australian fauna, from identical species, through identical genera, and allied genera, to distinct but allied families; clearly indicating very long continued yet rare immigations from Australia or Polynesia; immigrations which are continued down to our day. For resident ornithologists believe, that the _Zosterops lateralis_ has found its way to New Zealand within the last few years, and that the two cuckoos now migrate annually, the one from Australia, the other from some {453}part of Polynesia, distances of more than 1,000 miles! These facts seem, however, to have been accepted on insufficient evidence and to be in themselves extremely improbable. It is observed that the cuckoos appear annually in certain districts and again disappear; but their course does not seem to have been traced, still less have they ever been actually seen arriving or departing across the ocean. In a country which has still such wide tracts of unsettled land, it is very possible that the birds in question may only move from one part of the islands to another. _Islets of the New Zealand Sub-region._ We will here notice the smaller islands belonging to the sub-region, as it is chiefly their birds that possess any interest. _Norfolk Island._--The land-birds recorded from this island amount to 15 species, of which 8 are Australian, viz.: _Climacteris scandens_, _Symmorphus leucopygius_, _Zosterops tenuirostris_ and _Z. albogularis_, _Halcyon sanctus_, _Platycercus pennanti_, _Carpophaga spadicea_, _Phapspicata_ and _P. chalcoptera_. Of the peculiar species three belong to Australian genera; _Petroica_, _Gerygone_, and _Rhipidura_; one to a cosmopolitan genus, _Turdus_. So far the affinity seems to be all Australian, and there remain only three birds which ally this island to New Zealand,--_Nestor productus_, _Cyanoramphus rayneri_, and _Notornis alba_. The former inhabited the small Phillip Island (close to Norfolk Island) but is now extinct. Being a typical New Zealand genus, quite incapable of flying across the sea, its presence necessitates some former connexion between the two islands, and it is therefore perhaps of more weight than all the Australian genera and species, which are birds capable of long flights. The _Cyanoramphus_ is allied to a New Zealand broad-tailed parroquet. The _Notornis alba_ is extinct, but two specimens exist in museums, and it is even a stronger case than the _Nestor_, as showing a former approximation or union of this island with New Zealand. A beautiful figure of this bird is given in the _Ibis_ for 1873. _Lord Howe's Island._--This small island, situated half-way between Australia and Norfolk Island, is interesting, as containing a peculiar species of the New Zealand genus _Ocydromus_, or {454}wood-hen (_O. sylvestris_). There is also a peculiar thrush, _Turdus vinitinctus_. Its other birds are wholly of Australian types, and most of them probably Australian species. The following have been observed, and no doubt constitute nearly its whole indigenous bird fauna. _Acanthiza_ sp., _Rhipidura_ sp., _Pachycephala gutturalis_, _Zosterops strennuus_ and _Z. tephropleurus_, _Strepera_ sp., _Halcyon_ sp., and _Chalcophaga chrysochlora_. The two species of _Zosterops_ are peculiar. The _Ocydromus_ is important enough to ally this island to New Zealand rather than to Australia; and if the white bird seen there is, as supposed, the _Notornis alba_ which is extinct in Norfolk Island, the connection will be rendered still more clear. _Chatham Islands._--These small islands, 450 miles east of New Zealand, possess about 40 species of birds, of which 13 are land-birds. All but one belong to New Zealand genera, and all but five are New Zealand species. The following are the genera of the land-birds: _Sphenæacus_, _Gerygone_, _Myiomoira_, _Rhipidura_, _Zosterops_, _Anthus_, _Prosthemadera_, _Anthornis_, _Chrysococcyx_, _Cyanoramphus_, _Carpophaga_, _Circus_. The peculiar species are _Anthornis melanocephala_, _Myiomoira diffenbachi_ and _M. traversi_, _Rhipidura flabellifera_, and a peculiar rail incapable of flight, named by Captain Hutton _Cabalus modestus_. It is stated that the _Zosterops_ differs from that of New Zealand, and is also a migrant; and it is therefore believed to come every year from Australia, passing over New Zealand, a distance of nearly 1,700 miles! Further investigation will perhaps discover some other explanation of the facts. It is also stated, that the pigeon and one of the small birds (? _Gerygone_ or _Zosterops_) have arrived at the islands within the last eight years. The natives further declare, that both the _Stringops_ and _Apteryx_ once inhabited the islands, but were exterminated about the year 1835. _The Auckland Islands._--These are situated nearly 300 miles south of New Zealand, and possess six land-birds, of which three are peculiar,--_Anthus aucklandicus_, _Cyanoramphus aucklandicus_, and _C. malherbii_, the others being New Zealand species of _Myiomoira_, _Prosthemadera_, and _Anthornis_. It is remarkable that two peculiar parrots of the same genus should inhabit these small islands; but such localities seem favourable to the Platycercidæ, for another peculiar species is found in the remote Macquarie Islands, more than 400 miles farther south. A peculiar species and genus of ducks, _Nesonetta aucklandica_, is also found here, and as far as yet known, nowhere else. A species of the northern genus _Mergus_ is also found on these islands, and has been recently obtained by Baron von Hügel. Plate XIII. [Illustration] SCENE IN NEW ZEALAND, WITH SOME OF ITS REMARKABLE BIRDS. {455}_Plate XIII. Illustrating the peculiar Ornithology of New Zealand._--Our artist has here depicted a group of the most remarkable and characteristic of the New Zealand birds. In the middle foreground is the Owl-parrot or Kakapoe (_Stringops habroptilus_), a nocturnal burrowing parrot, that feeds on fern-shoots, roots, berries, and occasionally lizards; that climbs but does not fly; and that has an owl-like mottled plumage and facial disc. The wings however are not rudimentary, but fully developed; and it seems to be only the muscles that have become useless for want of exercise. This would imply, that these birds have not long been inhabitants of New Zealand only, but were developed in other countries (perhaps Australia) where their wings were of use to them. Beyond the Kakapoe are a pair of the large rails, _Notornis mantelli_; heavy birds with short wings quite useless for flight, and with massive feet and bill of a red colour. On the right is a pair of Kiwis (_Apteryx australis_), one of the queerest and most unbird-like of living birds. It has very small and rudimentary wings, entirely concealed by the hair-like plumage, and no tail. It is nocturnal, feeding chiefly on worms, which it extracts from soft earth by means of its long bill. The genus _Apteryx_ forms a distinct family of birds, of which four species are now known, besides some which are extinct. They are allied to the Cassowary and to the gigantic extinct _Dinornis_. On the wing are a pair of Crook-billed Plovers (_Anarhynchus frontalis_), remarkable for being the only birds known which have the bill bent sideways. This was at first thought to be a malformation; but it is now proved to be a constant character of the species, as it exists even in the young chicks; yet the purpose served by such an anomalous structure is not yet discovered. {456}No country on the globe can offer such an extraordinary set of birds as are here depicted. _Reptiles._--These consist almost wholly of lizards, there being no land-snakes and only one frog. Twelve species of lizards are known, belonging to three genera, one of which is peculiar, as are all the species. _Hinulia_, with two species, and _Mocoa_, with four species (one of which extends to the Chatham Islands), belong to the Scincidæ; both are very wide-spread genera and occur in Australia. The peculiar genus _Naultinus_, with six species, belongs to the Geckotidæ, a family spread over the whole world. The most extraordinary and interesting reptile of New Zealand is, however, the _Hatteria punctata_, a lizard-like animal living in holes, and found in small islands on the north-east coast, and more rarely on the main land. It is somewhat intermediate in structure between lizards and crocodiles, and also has bird-like characters in the form of its ribs. It constitutes, not only a distinct family, Rhyncocephalidæ, but a separate order of reptiles, Rhyncocephalina. It is quite isolated from all other members of the class; and is probably a slightly modified representative of an ancient and generalised form, which has been superseded in larger areas by the more specialized lizards and saurians. The only representatives of the Ophidia are two sea-snakes of Australian and Polynesian species, and of no geographical interest. _Amphibia._--The solitary frog indigenous to New Zealand, belongs to a peculiar genus, _Liopelma_, and to the family Bomburatoridæ, otherwise confined to Europe and temperate South America. _Fresh-water Fishes._--There are, according to Captain Hutton, 15 species of fresh-water fish in New Zealand, belonging to 7 genera; six species, and one genus (_Retropinna_), being peculiar. _Retropinna richardsoni_ belongs to the Salmonidæ, and is the only example of that family occurring in the Southern hemisphere, where it is confined to New Zealand and the Chatham Islands. The wide distribution of _Galaxias attenuatus_--from the {457}Chatham Islands to South America--has already been noticed; while another species, _G. fasciatus_, is found in the Chatham and Auckland Isles as well as New Zealand. A second genus peculiar to New Zealand, _Neochanna_, allied to _Galaxias_, has recently been described. _Prototroctes oxyrhynchus_ is allied to an Australian species, but belongs to a family (Haplochitonidæ) which is otherwise South American. An eel, _Anguilla latirostris_, is found in Europe, China, and the West Indies, as well as in New Zealand! while the genus _Agonostoma_ ranges to Australia, Celebes, Mauritius, and Central America. _Insects._--The great poverty of this class is well shown by the fact, that only eleven species of butterflies are known to inhabit New Zealand. Of these, six are peculiar, and one, _Argyrophenga_ (Satyridæ), is a peculiar genus allied to the Northern genus _Erebia_. The rest are either of wide range, as _Pyrameis cardui_ and _Diadema bolina_; or Australian, as _Hamdyaas zoilus_; while one, _Danais erippus_, is American, but has also occurred in Australia, and is no doubt a recent introduction into both countries. Only one _Sphinx_ is recorded, and no other species of the Sphingina except the British currant-moth, _Ægeria tipuliformis_, doubtless imported. Coleoptera are better represented, nearly 300 species having been described, all or nearly all being peculiar. These belong to about 150 genera, of which more than 50 are peculiar. No less than 14 peculiar genera belong to the Carabidæ, mostly consisting of one or two species, but _Demetrida_ has 3, and _Metaglymma_ 8 species. Other important genera are _Dicrochile_, _Homalosoma_, _Mecodema_, and _Scopodes_, all in common with Australia. _Mecodema_ and _Metaglymma_ are the largest genera. Even the Auckland Islands have two small genera of Carabidæ found nowhere else. Cicindelidæ are represented in New Zealand by 6 species of _Cicindela_, and 1 of _Dystipsidera_, a genus peculiar to the Australian region. The Lucanidæ are represented by two peculiar genera, _Dendroblax_ and _Oxyomus_; two Australian genera, _Lissotes_ and _Ceratognathus_; and by the almost cosmopolite _Dorcus_. The Scarabeidæ consist of ten species only, belonging to four {458}genera, two of which are peculiar (_Odontria_ and _Stethaspis_); and two Australian (_Pericoptus_ and _Calonota_). There are no Cetoniidæ. There is only one Buprestid, belonging to the Australian genus _Cisseis_. The Elateridæ, (about a dozen species,) belong mostly to Australian genera, but two, _Metablax_ and _Ochosternus_, are peculiar. There are 30 species of Curculionidæ, belonging to 22 genera. Of the genera, 12 are peculiar; 1 is common to New Zealand and New Caledonia; 5 belong to the Australian region, and the rest are widely distributed. Longicorns are, next to Carabidæ, the most numerous family, there being, according to Mr. Bates (_Ann. Nat. Hist._, 1874), about 35 genera, of which 26 are peculiar or highly characteristic, and 7 of the others Australian. The largest and most characteristic genera are _Æmona_ and _Xyloteles_, both being peculiar to New Zealand; few of the remainder having more than one or two species. _Demonax_ extends to the Moluccas and S. E. Asia. A dozen of the genera have no near relations with those of any other country. Phytophaga are remarkably scarce, only two species of _Colaspis_ being recorded; and there is only a single species of _Coccinella_. The other orders of Insects appear to be equally deficient. Hymenoptera are very poorly represented, only a score of species being yet known; but two of the genera are peculiar, as are all the species. The Neuroptera and Heteroptera are also very scarce, and several of the species are wide-spread forms of the Australian region. The few species of Homoptera are all peculiar. The Myriapoda afford some interesting facts. There are nine or ten species, all peculiar. One genus, _Lithobius_, ranges over the northern hemisphere as far south as Singapore, and probably through the Malay Archipelago, but is not found in Australia. _Henicops_ occurs elsewhere only in Tasmania and Chili. _Cryptops_, only in the north temperate zone; while two others, _Cermatia_ and _Cormocephalus_, both occur in Australia. {459}_Land-Shells._--Of these, 114 species are known, 97 being peculiar. Three species of _Helix_ are also found in Australia, and five more in various tropical islands of the Pacific. _Nanina_, _Lymnæa_, and _Assiminea_, are found in Polynesia or Malaya, but not in Australia. _Amphibola_ is an Australian genus, as is _Janella_. _Testacella_ and _Limax_ belong to the Palæarctic region. From the Chatham Islands, 82 species of shells are known, all being New Zealand species, except nine, which are peculiar. _The Ancient Fauna of New Zealand._--One of the most remarkable features of the New Zealand fauna, is the existence, till quite recent times, of an extensive group of wingless birds,--called Moas by the natives--many of them of gigantic size, and which evidently occupied the place which, in other countries, is filled by the mammalia. The most recent account of these singular remains, is that by Dr. Haast, who, from a study of the extensive series of specimens in the Canterbury museum, believes, that they belong to two families, distinguished by important differences of structure, and constitute four genera,--_Dinornis_ and _Miornis_, forming the family Dinornithidæ; _Palapteryx_ and _Euryapteryx_, forming the family Palapterygidæ. These were mostly larger birds than the living _Apteryx_, and some of them much larger even than the African ostrich, and were more allied to the Casuariidæ and Struthionidæ than to the Apterygidæ. No less than eleven species of these birds have been discovered; all are of recent geological date, and there are indications that some of them may have been in existence less than a century ago, and were really exterminated by man. Remains have been found (of apparently the same recent date) of species of _Apteryx_, _Stringops_, _Ocydromus_, and many other living forms, as well as of _Harpagornis_, a large bird of prey, and _Cnemiornis_, a gigantic goose. Bodies of the _Hatteria punctata_ have also been found along with those of the Moa, showing that this remarkable reptile was once more abundant on the main islands than it is now. _The Origin of the New Zealand Fauna._--Having now given {460}an outline sketch of the main features of the New Zealand fauna and of its relations with other regions, we may consider what conclusions are fairly deducible from the facts. As the outlying Norfolk, Chatham, and Lord Howe's Islands, are all inhabited (or have recently been so) by birds of New Zealand type or even identical species, almost incapable of flight, we may infer that these islands show us the former minimum extent of the land-area in which the peculiar forms which characterise the sub-region were developed. If we include the Auckland and Macquarie Islands to the south, we shall have a territory of not much less extent than Australia, and separated from it by perhaps several hundred miles of ocean. Some such ancient land must have existed to allow of the development and specialization of so many peculiar forms of birds, and it probably remained with but slight modifications for a considerable geological period. During all this time it would interchange many of its forms of life with Australia, and there would arise that amount of identity of genera between the two countries which we find to exist. Its extension southwards, perhaps considerably beyond the Macquaries, would bring it within the range of floating ice during colder epochs, and within easy reach of the antarctic continent during the warm periods; and thus would arise that interchange of genera and species with South America, which forms one of the characteristic features of the natural history of New Zealand. Captain F. W. Hutton (to whose interesting paper on the Geographical relations of the New Zealand Fauna we are indebted for some of our facts) insists upon the necessity of former land-connections in various directions, and especially of an early southern continental period, when New Zealand, Australia, Southern Africa, and South America, were united. Thus he would account for the existence of Struthious birds in all these countries, and for the various other groups of birds, reptiles, fishes, or insects which have no obvious means of traversing the ocean,--and this union must have occurred before mammalia existed in any of these countries. But such a supposition is quite unnecessary, if we consider that all wingless land-birds and some water-birds (as the Gare-fowl {461}and Steamer Duck) are probably cases of abortion of useless organs, and that the common ancestors of the various forms of Struthiones may have been capable of a moderate degree of flight; or they may have originated in the northern hemisphere, as already explained in Chap. XI. p. 287. The existence of two, if not three, distinct families of these birds in New Zealand, proves that the original type was here isolated at a very early date, and being wholly free from the competition of mammalia, became more differentiated than elsewhere. The _Hatteria_ is probably coeval with these early forms, and is the only relic of a whole order of reptiles, which once perhaps ranged far over the globe. Still less does any other form of animal inhabiting New Zealand, require a land connection with distant countries to account for its presence. With the example before us of the Bermudas and Azores, to which a great variety of birds fly annually over vast distances, and even of the recent arrival of new birds in New Zealand and Chatham Island, we may be sure that the ancestors of every New Zealand bird could easily have reached its shores during the countless ages which elapsed while the _Dinornis_ and _Apteryx_ were developing. The wonderful range of some of the existing species of lizards and fresh-water fish, as already given, proves that they too possess means of dispersal which have sufficed to spread them, within a comparatively recent period, over countries separated by thousands of miles of ocean; and the fact that a group like the snakes, so widely distributed and for which the climate of New Zealand is so well adapted, does not exist there, is an additional proof that land connection had nothing to do with the introduction of the existing fauna. We have already (p. 398), discussed in some detail the various modes in which the dispersal of animals in the southern hemisphere has been effected; and in accordance with the principles there established, we conclude, that the New Zealand fauna, living and extinct, demonstrates the existence of an extensive tract of land in the vicinity of Australia, Polynesia, and the Antarctic continent, without having been once actually connected with either of these countries, since the period when mammalia had peopled {462}all the great continents. That event certainly dates back to Secondary, if not to Palæozoic, times, because so dominant a group must soon have spread over the whole continuous land-area of the globe. We have no reason for believing that birds were an earlier development; and certainly cannot, with any probability, place the origin of the Struthiones before that of Mammals. _Causes of the Poverty of Insect-life in New Zealand: its Influence on the Character of the Flora._--The extreme paucity of insects in New Zealand, to which we have already alluded, seems to call for some attempt at explanation. No other country in the world, in which the conditions are equally favourable for insect-life, and which has either been connected with, or is in proximity to, any of the large masses of land, presents a similar phenomenon. The only approach to it is in the Galapagos, and in some of the islands of the Pacific; and in each of these cases the absence of mammals leads us to infer, that no connection with a continent has ever taken place. Yet the fauna of New Zealand evidently dates back to a remote geological epoch, and it seems strange that an abundance of indigenous insects have not been developed, especially when we consider the vast antiquity that most of the orders and families, and many of the genera, of insects possess (see p. 166), and that they must always have reached the country in greater numbers and variety than any of the higher animals. The undoubted fact that such an indigenous insect-fauna has not arisen, would therefore lead us to conclude, that insects find the conditions requisite for their development only in the great continental masses of land, in strict adaptation to, and dependance on, a varied fauna and flora of ever-increasing richness and complexity. A small number of widely-separated forms, introduced into a country where the fauna and flora are alike scanty and unrelated to them, seem to have little tendency to vary and branch out into that vast network of insect-life which enriches all the great continents and their once connected islands. It is a striking confirmation on a large scale, of Mr. Darwin's beautiful theory--that the gay colours of flowers have mostly, or {463}perhaps, wholly been produced, in order to attract insects which aid in their fertilization--that in New Zealand, where insects are so strikingly deficient in variety, the flora should be almost as strikingly deficient in gaily-coloured blossoms. Of course there are some exceptions, but as a whole, green, inconspicuous, and imperfect flowers prevail, to an extent not to be equalled in any other part of the globe; and affording a marvellous contrast to the general brilliancy of Australian flowers, combined with the abundance and variety of its insect-life. We must remember, too, that the few gay or conspicuous flowering-plants possessed by New Zealand, are almost all of Australian, South American, or European _genera_; the peculiar New Zealand or Antarctic genera being almost wholly without conspicuous flowers. In the tropical Galapagos the same thing occurs. Mr. Darwin notices the wretched weedy appearance of the vegetation; and states that it was some time before he discovered that most of the plants were in flower at the time of his visit! And the insect-life was correspondingly deficient, consisting mainly of a few terrestrial beetles. The poverty of insect-life in New Zealand must, therefore, be a very ancient feature of the country; and it furnishes an additional argument against the theory of land-connection with, or even any near approach to, either Australia, South Africa, or South America. For in that case numbers of winged insects would certainly have entered, and the flowers would then, as in every other part of the world, have been rendered attractive to them by the development of coloured petals; and this character once acquired would long maintain itself, even if the insects had, from some unknown cause, subsequently disappeared. After the preceding paragraphs were written, it occurred to me, that if this reasoning were correct, New Zealand plants ought to be also deficient in scented flowers; because it is a part of the same theory, that the odours of flowers have, like their colours, been developed to attract the insects required to aid in their fertilization. I therefore at once applied to my friend Dr. Hooker, as the highest authority on New Zealand botany; simply asking whether there was any such observed deficiency. His reply {464}was:--"New Zealand plants are remarkably scentless, both in regard to the rarity of scented flowers, of leaves with immersed glands containing essential oils, and of glandular hairs." There are a few exceptional cases, but these seem even more rare than might be expected, so that the confirmation of theory is very complete. The circumstance that aromatic leaves are also very scarce, suggests the idea that these, too, serve as an attraction to insects. Aromatic plants abound most in arid countries, and on Alpine heights; both localities where winged insects are comparatively scarce, and where it may be necessary to attract them in every possible way. Dr. Hooker also informs, me that since his _Introduction to the New Zealand Flora_ was written, many plants with handsome flowers have been discovered, especially among the _Ranunculi_, shrubby Veronicas, and herbaceous Compositæ. The two former, however, are genera of wide range, which may have originated in New Zealand by the introduction of plants with handsome flowers, which the few indigenous insects would be attracted by, and thus prevent the loss of their gay corollas; so that these discoveries will not much affect the general character of the flora, and its very curious bearing on the past history of the islands through the relations of flowers and insects. In judging of the relation here supposed to exist, it must be remembered, that if the New Zealand insects have been introduced from the surrounding countries by chance immigrations at distant intervals, then, as we go back into the past the insect fauna will become poorer and poorer, and still more inadequate than at present to lead to the development of attractive flowers and odours. This quite harmonizes with the fact of the ancient indigenous flora being so remarkably scentless and inconspicuous, while a few of the more recently introduced genera of plants have retained their floral attractions. _Concluding Remarks on the Early History of the Australian Region._ We have already discussed in some detail, the various relations of the Australian sub-regions to the surrounding Regions, and the geographical changes that appear to have taken place. A very {465}few observations will therefore suffice, on the supposed early history of the Australian region as a whole. It was probably far back in the Secondary period, that some portion of the Australian region was in actual connection with the northern continent, and became stocked with ancestral forms of Marsupials; but from that time till now there seems to have been no further land connection, and the Australian lands have thenceforward gone on developing the Marsupial and Monotremate types, into the various living and extinct races we now find there. During some portion of the Tertiary epoch Australia probably comprised much of its existing area, together with Papua and the Solomon Islands, and perhaps extended as far east as the Fiji Islands; while it might also have had a considerable extension to the south and west. Some light has recently been thrown on this subject by Professor McCoy's researches on the Palæontology of Victoria. He finds abundant marine fossils of Eocene and Miocene age, many of which are strikingly similar to those of Europe at the same period. Among these are Cetaceans of the genus _Squalodon_; European species of Plagiostomous fishes; mollusca and corals closely resembling those of Europe and North America of the same age,--such as numerous Volutes closely allied to those of the Eocene beds of the Isle of Wight, and the genus _Dentalium_ in great abundance, almost or quite identical with European tertiary species. Along with these, are found some living species, but always such as now live farther north in tropical seas. The Cretaceous and Mesozoic marine fossils are equally close to those of Europe. The whole of these remains demonstrate that, as in the northern so in the southern hemisphere, a much warmer climate prevailed in the Eocene and Miocene periods than at the present time. This is a most important result, and one which strongly supports Mr. Belt's view, before referred to, that the warmer climates in past geological epochs, and especially that of the Miocene as compared with our own, was caused by a diminution of the obliquity of the ecliptic, leading to a much greater uniformity of the seasons for a considerable distance from the equator, and greatly reducing the polar area within which the sun would ever {466}disappear during an entire rotation of the earth. During such a period, tropical forms of marine animals would have been able to spread north and south, into what are now cool latitudes; and identical genera, and even species, might then have ranged along the southern shores of the old Palæarctic continent, from Britain to the Bay of Bengal, and southward along the Malayan coasts to Australia, Numerous Miocene plant-beds have also been found in Victoria, containing abundance of Dicotyledonous leaves, which are said generally to resemble those of the Asiatic flora, and of the Miocene plant-beds of the Rhine. It is to be hoped these beds will be more closely examined for remains of insects, land-shells, and vertebrates, and that the plants will be carefully preserved and critically studied; for here probably lies hidden the key, that will solve much of the mystery that attaches to the past history of the Australian fauna. {467}TABLES OF DISTRIBUTION. In drawing up these tables, showing the distribution of the various classes of animals in the Australian region, the following sources of information have been relied on, in addition to the general treatises, monographs, and catalogues used in compiling the 4th Part of this work. _Mammalia._--Gould, Mammals of Australia; Waterhouse on Marsupials; Dr. J. E. Gray's List of Mammalia of New Guinea; Müller, Temminck and Schlegel on Mammals of the Moluccas; papers by Dr. Gray; and personal observations by the Author. _Birds._--Gould's Birds of Australia; Buller's Birds of New Zealand; G. R. Gray's Lists of Birds of Moluccas, &c. Hartlaub and Finsch on Birds of Pacific Islands; Sclater on Birds of Sandwich Islands; papers by Haast, Hutton, Meyer, Salvin, Schlegel, Sclater, Travers, Lord Walden and the Author. _Reptiles._--Krefft, Catalogue of Snakes; Gunther, List of Lizards in _Voyage of Erebus and Terror_ (1875); and numerous papers. {468}TABLE I. _FAMILIES OF ANIMALS INHABITING THE AUSTRALIAN REGION._ EXPLANATION. Names in _italics_ show families which are peculiar to the region. Names inclosed thus (...) show families which only just enter the region, and are not considered properly to belong to it. Numbers correspond to the series of numbers to the families in Part IV. ---------------------+-------------------+------------------------------- | Sub-regions | | 1=Austro-Malaya. | Order and Family | 2=Australia. | Range beyond the Region. | 3=Polynesia. | | 4=New Zealand. | ---------------------+----+----+----+----+------------------------------- | 1. | 2. | 3. | 4. | ---------------------+----+----+----+----+------------------------------- | | | | | MAMMALIA. | | | | | PRIMATES. | | | | | 3. Cynopithecidæ | -- | | | |Oriental and Ethiopian | | | | | CHIROPTERA. | | | | | 9. Pteropidæ | -- | -- | -- | -- |Oriental and Ethiopian 11. Rhinolophidæ | -- | -- | | |The Eastern Hemisphere 12. Vespertilionidæ | -- | -- | -- | -- |Cosmopolite 13. Noctilionidæ | | | | -- |All tropical regions | | | | | CARNIVORA. | | | | | 25. (Viverridæ) | -- | | | |Oriental 33. Otariidæ | | -- | | -- |N. and S. temperate zones 35. Phocidæ | | -- | | -- |N. and S. temperate zones | | | | | CETACEA. | | | | | 36 to 41. | | | | |Oceanic | | | | | SIRENIA. | | | | | 42. Manatidæ | -- | | | |Ethiopian, Oriental | | | | | UNGULATA. | | | | | 47. Suidæ | -- | | | |All other regions but Nearctic 50. (Cervidæ) | -- | | | |All other regions but Ethiopian 52. (Bovidæ) | -- | | | |All other regions but | | | | | Neotropical | | | | | RODENTIA. | | | | | 55. Muridæ | -- | -- | | |All other regions 61. (Scuiridæ) | -- | | | |All other regions | | | | | MARSUPIALIA. | | | | | 77. _Dasyuridæ_ | -- | -- | | | 78. _Myrmecobiidæ_ | | -- | | | 79. _Peramelidæ_ | -- | -- | | | 80. _Macropodidæ_ | -- | -- | | | 81. _Phalangistidæ_ | -- | -- | | | 82. _Phascolomyidæ_ | | -- | | | | | | | | MONOTREMATA. | | | | | 83._Ornithorhynchidæ_| | -- | | | 84. _Echidnidæ_ | | -- | | | | | | | | BIRDS. | | | | | PASSERES. | | | | | 1. Turdidæ | -- | -- | -- | |Cosmopolite 2. Sylviidæ | -- | -- | -- | -- |Cosmopolite 3. Timaliidæ | -- | -- | | -- |Oriental family 5. Cinclidæ | -- | | | | 8. Certhiidæ | -- | -- | | | 9. Sittidæ | -- | -- | | -- | 10. Paridæ | | -- | | -- | 13. Pycnonotidæ | -- | | | |Oriental family 14. Oriolidæ | -- | -- | | |Oriental and Ethiopian 15. Campephagidæ | -- | -- | -- | -- |Oriental and Ethiopian 16. Dicruridæ | -- | -- | | |Oriental and Ethiopian 17. Muscicapidæ | -- | -- | -- | -- |The Old World 18. _Pachycephalidæ_| -- | -- | -- | |Almost peculiar to region 19. Laniidæ | -- | -- | -- | |The Old World 20. Corvidæ | -- | -- | -- | |Cosmopolite 21. _Paradiseidæ_ | -- | -- | | | 22. _Meliphagidæ_ | -- | -- | -- | -- | 23. Nectariniidæ | -- | -- | | |Oriental and Ethiopian 24. Dicæidæ | -- | -- | -- | -- |Oriental and Ethiopian 25. _Drepanididæ_ | | | -- | | 30. Hirundinidæ | -- | -- | -- | -- |Cosmopolite 34. Ploceidæ | -- | -- | -- | |Oriental, Ethiopian 35. Sturnidæ | -- | | -- | -- |The Old World 36. Artamidæ | -- | -- | -- | |Oriental 37. Alaudidæ | -- | -- | | |The Old World and N. America 38. Motacillidæ | -- | -- | | -- |The Old World 47. Pittidæ | -- | -- | | |Oriental, Ethiopian 49. _Menuridæ_ | | -- | | |Peculiar to Australia 50. _Atrichiidæ_ | | -- | | |Peculiar to Australia | | | | | PICARIÆ. | | | | | 51. Picidæ | -- | | | |All other regions 58. Cuculidæ | -- | -- | -- | -- |Cosmopolite 62. Coraciidæ | -- | -- | | |Oriental and Ethiopian 63. Meropidæ | -- | -- | | |Oriental and Ethiopian 67. Alcedinidæ | -- | -- | -- | -- |Cosmopolite 68. Bucerotidæ | -- | | | |Oriental and Ethiopian 71. Podargidæ | -- | -- | | |Oriental 73. Caprimulgidæ | -- | -- | -- | |Cosmopolite 74. Cypselidæ | -- | -- | -- | |Cosmopolite | | | | | PSITTACI. | | | | | 76. _Cacatuidæ_ | -- | -- | | |Philippine Islands 77. _Platycercidæ_ | -- | -- | -- | -- | 78. Palæornithidæ | -- | | | |Oriental 79. _Trichoglossidæ_| -- | -- | -- | | 82. _Nestoridæ_ | -- | | | -- | 83. _Stringopidæ_ | | | | -- | | | | | | COLUMBÆ. | | | | | 84. Columbidæ | -- | -- | -- | -- |Cosmopolite 84a. _Didunculidæ_ | | | -- | | | | | | | GALLINÆ. | | | | | 87. Tetraonidæ | -- | -- | -- | -- |Old World and N. America 88. (Phasianidæ) | -- | | | |Oriental 89. Turnicidæ | -- | -- | | |The Old World 90. _Megapodiidæ_ | -- | -- | -- | | | | | | | ACCIPITRES. | | | | | 96. Falconidæ | -- | -- | -- | -- |Cosmopolite 97. Pandionidæ | -- | -- | -- | -- |Cosmopolite 98. Strigidæ | -- | -- | -- | -- |Cosmopolite | | | | | GRALLÆ. | | | | | 99. Rallidæ | -- | -- | -- | -- |Cosmopolite 100. Scolopacidæ | -- | -- | -- | -- |Cosmopolite 103. Parridæ | -- | -- | | |Tropical 104. Glareolidæ | -- | -- | | |The Eastern Hemisphere 105. Charadriidæ | -- | -- | -- | -- |Cosmopolite 106. Otididæ | | -- | | |The Eastern Hemisphere 107. Gruidæ | | -- | | |The Eastern Hemisphere 112. _Rhinochetidæ_ | | | -- | | 113. Ardeidæ | -- | -- | -- | -- |Cosmopolite 114. Plataleidæ | -- | -- | | |Almost cosmopolite 115. Ciconiidæ | -- | -- | | |Widely distributed | | | | | ANSERES. | | | | | 118. Anatidæ | -- | -- | -- | -- |Cosmopolite 119. Laridæ | -- | -- | -- | -- |Cosmopolite 120. Procellariidæ | -- | -- | -- | -- |Cosmopolite 121. Pelecanidæ | -- | -- | -- | -- |Cosmopolite 122. Spheniscidæ | | -- | | -- |S. temperate regions 124. Podicipidæ | -- | -- | -- | -- |Cosmopolite | | | | | STRUTHIONES. | | | | | 127. _Casuariidæ_ | -- | -- | | | 128. _Apterygidæ_ | | | | -- | 129. _Dinornithidæ_ | | | | -- |Extinct 130. _Palapterygidæ_ | | | | -- |Extinct | | | | | REPTILIA. | | | | | OPHIDIA. | | | | | 1. Typhlopidæ | -- | -- | | |All regions but Nearctic 2. Tortricidæ | -- | | | |Oriental, S. America, | | | | | California 3. Xenopeltidæ | -- | | | |Oriental 5. Calamariidæ | -- | -- | | |All warm countries 7. Colubridæ | -- | -- | | |Almost cosmopolite 8. Homalopsidæ | -- | -- | | |Oriental, and all other regions 11. Dendrophidæ | -- | -- | | |Oriental, Ethiopian, | | | | | Neotropical 12. Dryiophidæ | -- | | | |Oriental, Ethiopian, | | | | | Neotropical 13. Dipsadidæ | -- | -- | | |Oriental, Ethiopian, | | | | | Neotropical 15. Lycodontidæ | -- | | | |Ethiopian and Oriental 16. Amblycephalidæ | | -- | | |Oriental, Neotropical 17. Pythonidæ | -- | -- | -- | |Tropical regions, California 19. Acrochordidæ | -- | | | |Oriental 20. Elapidæ | -- | -- | -- | |Tropical regions, Japan, | | | | | S. Carolina 23. Hydrophidæ | -- | -- | -- | -- |Oriental, Madagascar, Panama | | | | | LACERTILIA. | | | | | 30. Varanidæ | -- | -- | | |Oriental, Africa 33. Lacertidæ | | -- | | |The Eastern Hemisphere 41. Gymnopthalmidæ | -- | -- | -- | |Neotropical, Ethiopian, | | | | | Palæarctic 42. _Pygopodidæ_ | | -- | | | 43. _Aprasiadæ_ | | -- | | | 44. _Lialidæ_ | | -- | | | 45. Scincidæ | -- | -- | -- | -- |Almost cosmopolite 48. Acontiadæ | -- | | | |Ethiopian, Oriental 49. Geckotidæ | -- | -- | -- | -- |Almost cosmopolite 50. Iguanidæ | | | -- | |N. and S. America 51. Agamidæ | -- | -- | -- | |The Eastern Hemisphere | | | | | RHYNCOCEPHALINA. | | | | | 53._Rhyncocephalidæ_ | | | | -- | | | | | | CROCODILIA. | | | | | 54. Gavialidæ | -- | | | |Oriental 55. Crocodilidæ | -- | -- | | |Tropical regions | | | | | CHELONIA. | | | | | 57. Testudinidæ | -- | | | |All other regions 58. Chelydidæ | -- | -- | | |Ethiopian, Neotropical 60. Cheloniidæ | -- | -- | -- | -- |Marine | | | | | AMPHIBIA. | | | | | ANOURA. | | | | | 7. Phryniscidæ | | -- | | |Ethiopian, Malayan, Neotropical 9. Bufonidæ | -- | | | |All other regions 10. _Xenorhinidæ_ | -- | | | | 11. Engystomidæ | | -- | | |All regions but Palæarctic 12. Bombinatoridæ | | | | -- |Neotropical, Palæarctic 14. Alytidæ | -- | -- | | |All regions but Oriental 15. Pelodryadæ | -- | -- | | |Neotropical 16. Hylidæ | -- | -- | | |All regions but Ethiopian 17. Polypedatidæ | -- | -- | -- | |All the regions 18. Ranidæ | -- | -- | | |Almost cosmopolite 19. Discoglossidæ | -- | -- | | |All regions but Nearctic | | | | | FISHES (FRESH-WATER).| | | | | ACANTHOPTERYGII. | | | | | 11. Trachinidæ | | -- | | |Patagonia (? marine) 35. Labyrinthici | -- | | | |Oriental, S. Africa 37. Atherinidæ | | -- | | |Europe, America 38. Mugillidæ | -- | -- | | -- |Ethiopian, Neotropical | | | | | ANACANTHINI. | | | | | 53. _Gadopsidæ_ | | -- | | | | | | | | PHYSOSTOMI. | | | | | 59. Siluridæ | -- | -- | -- | -- |All warm regions 61. Haplochitonidæ | | -- | | |Temperate S. America 65. Salmonidæ | | | | -- |Palæarctic, Nearctic 67. Galaxidæ | | -- | | -- |Temperate S. America 78. Osteoglossidæ | | -- | | |All tropical regions 85. (Symbranchidæ) | | -- | | |Oriental, Neotropical | | | | | DIPNOI. | | | | | 92. Sirenoidei | | -- | | |Ethiopian, Neotropical | | | | | INSECTS. | | | | | LEPIDOPTERA (PART). | | | | | DIURNI (BUTTERFLIES).| | | | | 1. Danaidæ | -- | -- | -- | -- |All warm regions, and to Canada 2. Satyridæ | -- | -- | -- | -- |Cosmopolite 3. Elymniidæ | -- | | | |Oriental, Ethiopian 4. Morphidæ | -- | | -- | |Oriental, Neotropical 6. Acræidæ | -- | -- | | |All tropical regions 8. Nymphalidæ | -- | -- | -- | -- |Cosmopolite 9. Libytheidæ | -- | | | |All the other regions 10. Nemeobeidæ | -- | | | |All other regions but Nearctic 13. Lycænidæ | -- | -- | -- | -- |Cosmopolite 14. Pieridæ | -- | -- | -- | -- |Cosmopolite 15. Papilionidæ | -- | -- | -- | -- |Cosmopolite 16. Hesperidæ | -- | -- | -- | -- |Cosmopolite | | | | | SPHINGIDEA. | | | | | 17. Zygænidæ | -- | -- | -- | -- |Cosmopolite 18. Castniidæ | -- | -- | -- | -- |Neotropical 19. Agaristidæ | -- | -- | -- | -- |Oriental, Ethiopian 20. Uraniidæ | -- | -- | -- | -- |All tropical regions 23. Sphingidæ | -- | -- | -- | -- |Cosmopolite TABLE II. _GENERA OF TERRESTRIAL MAMMALIA AND BIRDS INHABITING THE AUSTRALIAN REGION._ EXPLANATION. Names in _italics_ show genera peculiar to the region. Names enclosed thus (...) show genera which just enter the region, but are not considered properly to belong to it. Genera truly belonging to the region are numbered consecutively. _MAMMALIA._ -------------------+-------+----------------------+---------------------- Order, Family, and | No. of| Range within | Range beyond Genus. |Species| the Region. | the Region. -------------------+-------+----------------------+---------------------- | | | PRIMATES. | | | CYNOPITHECIDÆ. | | | | | | (Macacus | 1 |Lombok to Timor) |Oriental genus 1. Cynopithecus | 1 |Celebes and Batchian |Philippines? | | | LEMURIDÆ. | | | | | | (Tarsius | 1 |Celebes) |Indo-Malayan genus | | | CHIROPTERA. | | | PTEROPIDÆ. | | | | | | 2. Pteropus | 15 |The whole reg. except |Tropics of E. Hemisp. | | New Zeal. | 3. Xantharpyia | 1 |Moluccas and Timor |Oriental, | | | S. Palæarctic 4. Cynopterus | 1 |Morty Island |Oriental 5. Macroglossus | 1 |Celebes, Moluccas, |Indo-Malaya | | Timor | 6. Harpyia | 1 |Celebes and Moluccas |Philippines 7. _Hypoderma_ | 1 |Celebes, Moluccas, and | | | Timor | 8. _Notopteris_ | 1 |Fiji Islands | | | | RHINOLOPHIDÆ. | | | | | | 9. Rhinolophus | 7 |Moluccas, Timor, |Warmer pts. of | | Australia | E. Hemis. 10. Hipposideros | 5 |Moluccas and Aru |Oriental | | Islands | 11. Phyllorhina | 2 |Moluccas and Timor |Indo-Malaya 12. Asellia | 1 |Amboyna |Indo-Malaya 13. Megaderma | 1 |Ternate |Oriental, Ethiopian | | | VESPERTILIONIDÆ. | | | | | | 14. Scotophilus | 8 |Moluccas, Timor, |Oriental | | Australia | 15. Vespertilio | 2 |Australia |Cosmopolite 16. Miniopteris | 3 |Moluccas, Timor, and |Indo-Malaya, S. Africa | | Australia | 17. Taphozous | 2 |Celebes, Moluccas, |Orien., Ethiop., | | N. Australia | Neotrop. 18. Plecotus | 1 |Timor |N. India, | | | S. Palæarctic 19. Nyctophilus | 5 |Australia and Tasmania |India | | | NOCTILIONIDÆ. | | | | | | 20. Molossus | 1 |Australia |Neotrop., Ethiop., | | | S. Pal. 21. _Mystacina_ | 1 |New Zealand | | | | INSECTIVORA. | | | SORICIDÆ. | | | | | | 22. Sorex | 2 |Moluccas and Timor |The E. Hemis. & | | | N. Amer. | | | CARNIVORA. | | | VIVERRIDÆ. | | | | | | (Viverra | 1 |Celebes and Moluccas) |Oriental genus (Paradoxurus | 1 |Timor, Ke Islands, ? |Oriental genus | | introduced) | | | | OTARIIDÆ. | | | | | | 23. Arctocephalus | 1 |S. Australia, |S. Temperate shores | | New Zealand | 24. Zalophus | 1 |Australia |North Pacific | | | PHOCIDÆ. | | | | | | 25. Stenorhynchus | 1 |New Zealand |Antarctic shores | | | SIRENIA. | | | MANATIDÆ. | | | | | | 26. Halicore | 1 |N. Australia |Oriental Ethiopian | | | UNGULATA. | | | SUIDÆ. | | | | | | 27. Sus | 4 |Celebes to New Guinea |Palæarctic, Oriental 28. _Babirusa_ | 1 |Celebes, Bouru | | | | CERVIDÆ. | | | | | | (Cervus | 2 |Celebes, Moluccas, |Oriental genus | | Timor) | | | | BOVIDÆ. | | | | | | 29. _Anoa_ | 1 |Celebes | | | | RODENTIA. | | | SCIURIDÆ. | | | | | | (Sciurus | 5 |Celebes) |All the other regions | | | MURIDÆ. | | | | | | 30. Mus | 13 |Australia, Celebes, |The Western Hemisphere | | Papua | 31. _Pseudomys_ | 1 |Australia | 32. _Hapalotis_ | 13 |Australia | 33. _Hydromys_ | 5 |Australia and Tasmania | 34. _Acanthomys_ | 1 |N. Australia | 35. _Echiothrix_ | 1 |Australia | | | | MARSUPIALIA. | | | DASYURIDÆ. | | | | | | 36. _Phascogale_ | 3 |New Guinea and | | | Australia | 37. _Antechinomys_ | 1 |S. Australia (interior)| 38. _Antechinus_ | 12 |Aru Ids. Australia and | | | Tasmania | 39. _Chætocercus_ | 1 |S. Australia | 40. _Dactylopsila_ | 1 |Aru Islands and | | | N. Australia | 41. _Podabrus_ | 5 |Australia and Tasmania | 42. _Myoictis_ | 1 |Aru Islands | 43. _Sarcophilus_ | 1 |Tasmania | 44. _Dasyurus_ | 4 |Australia | 45. _Thylacinus_ | 1 |Tasmania | | | | MYRMECOBIIDÆ. | | | | | | 45. _Myrmecobius_ | 1 |S. and W. Australia | | | | PERAMELIDÆ. | | | | | | 47. _Perameles_ | 8 |N. Guinea, Aru Ids., | | |Australia, and Tasmania| 48. _Peragalea_ | 1 |W. Australia | 49. _Chæropus_ | 1 |S. E. and W. Australia | | | | MACROPODIDÆ. | | | | | | 50. _Macropus_ | 4 |Australia and Tasmania | 51. _Osphranter_ | 5 |All Australia | 52. _Halmaturus_ | 18 |Australia and Tasmania | 53. _Petrogale_ | 7 |All Australia | 54. _Dendrolagus_ | 2 |New Guinea | 55. _Dorcopsis_ | 2 |Aru, Mysol, and | | | N. Guinea | 56. _Onychogalea_ | 3 |Central Australia | 57. _Lagorchestes_ | 5 |N., W., and S. | | | Australia | 58. _Bettongia_ | 6 |W., S., and E. | | | Australia and Tasmania| 59. _Hypsiprymnus_ | 4 |W. and E. Australia & | | | Tasmania | | | | PHALANIGISTIDÆ. | | | | | | 60. _Phascolarctos_ | 1 |E. Australia | 61. _Phalangista_ | 5 |E., S., and W. | | | Australia and Tasmania| 62. _Cuscus_ | 8 |Celebes to N. Guinea, | | | Timor & N. Australia | 63. _Petaurista_ | 1 |E. Australia | 64. _Belideus_ | 5 |S., E., & N. Austral., | | |N. Guinea, and Moluccas| 65. _Acrobata_ | 1 |S. and E. Australia | 66. _Dromicia_ | 5 |W. & E. Australia & | | | Tasmania | 67. _Tarsipes_ | 1 |W. Australia | | | | PHASCOLOMYIDÆ. | | | | | | 63. _Phascolomys_ | 1 |S. E. Australia and | | | Tasmania | | | | MONOTREMATA. | | | ORNITHORHYNCHIDÆ. | | | | | | 69._Ornithorhynchus_| 1 |S. and E. Australia & | | | Tasmania | | | | ECHIDNIDÆ. | | | | | | 70. _Echidna_ | 2 |S. & E. Australia, & | | | Tasmania | _BIRDS._ | | | PASSERES. | | | TURDIDÆ. | | | | | | 1. Turdus | 6 |Timor, Austral., New |Cosmopolite | | Caledonia, Norfolk | | | Island, Lord Howe's | | | and Samoan Islands | 2. Oreocincla | 1 |S. E. Australia and |Palæarctic, Oriental | | Tasmania | 3. Geocichla | 4 |Celebes, Lombok, Timor,|Oriental | | Austral. | (Monticola | 1 |Gilolo, Celebes) |Palæarctic and | | | Oriental (Zoothera | 1 |Lombok) |Oriental genus | | | SYLVIIDÆ. | | | | | | 4. Cisticola | 7 |Celebes, Bouru, Timor, |Palæarctic, Oriental | | Australia | 5. Sphenæacus | 4 |Australia, N. Zealand, |Ethiopian | | Chatham Islands | 6. Megalurus | 1 |Timor |Oriental 7. _Poodytes_ | 2 |Australia | 8. _Amytis_ | 3 |Australia | 9. _Sphenura_ | 4 |Australia | 10. _Stipiturus_ | 1 |Australia, Tasmania | 11. _Malurus_ | 16 |Australia, Tasmania, & | | | N. Guinea | 12. _Hylacola_ | 3 |Australia | 13. _Calamanthus_ | 2 |Australia and Tasmania | 14. Acrocephalus | 7 |Celebes, Moluccas, |Palæarc., Orien., | | Australia, Caroline | Ethiop. | | Islands | 15. _Tatare_ | 2 |Samoan to Marquesas | | | Islands | 16. Hypolais | 1 |Moluccas |Palæarc., Orien., | | | Ethiop. 17. _Sericornis_ | 7 |Australia and Tasmania | 18. _Acanthiza_ | 14 |Austral., Tasmania, | | | N. Caledonia | 19. _Gerygone_ | 24 |The whole region, excl.|Philippines | | Moluccas | 20. _Drymodes_ | 2 |Australia | 21. Oreicola | 4 |Lombok to Timor |Burmah ? (Pratincola | 1 |Celebes to Timor) |Oriental, Palæarctic 22. _Epthianura_ | 3 |Australia | 23. _Petroica_ | 18 |Papua to Samoan Ids., | | | Australia | 24. _Myiomoira_ | 3 |N. Zealand | 25. _Lamprolia_ | 1 |Fiji Islands | 26. _Miro_ | 3 |New Zealand | 27._Cinclorhamphus_| 2 |Australia | 28. _Origma_ | 1 |Australia | 29. _Orthonyx_ | 5 |N. Guinea, Austral., | | | New Zeald. | | | | TIMALIIDÆ. | | | | | | 30. Pomatorhinus | 5 |N. Guinea and Australia|Oriental 31. _Cinclosoma_ | 4 |Australia and Tasmania | 32. _Turnagra_ | 3 |New Zealand | 33. _Psophodes_ | 2 |S. E. and W. Australia | 34. Alcippe | 3 |New Guinea |Oriental (Trichastoma | 1 |Celebes) |Oriental genus 35. Drymocataphus | 1 |Timor |Oriental 36. _Struthidea_ | 1 |N. and E. Australia | | | | CINCLIDÆ. | | | | | | 37. Eupetes | 2 |New Guinea |Malayan | | | CERTHIIDÆ. | | | | | | 38. _Climacteris_ | 8 |Australia and N. Guinea| | | | SITTIDÆ. | | | | | | 39. _Sittella_ | 5 |Australia and N. Guinea| 40. _Acanthisitta_ | 1 |New Zealand | 41. _Xenicus_ | 3 |New Zealand | | | | PARIDÆ. | | | | | | 42. _Certhiparus_ | 2 |New Zealand | 43. _Sphenostoma_ | 2 |E. and S. Australia | | | | PYCNONOTIDÆ. | | | | | | 44. Criniger | 5 |Moluccas, and small |Oriental | | islands E. of Celebes| | | | ORIOLIDÆ. | | | | | | 45. _Sphecotheres_ | 3 |Timor and Australia | 46. Oriolus | 3 |Celebes, Sulla Ids., |Oriental, Ethiopian | | Lombok and Flores | 47. _Mimeta_ | 10 |Moluccas, N. Guinea, | | | Timor, & Australia | | | | CAMPEPHAGIDÆ. | | | | | | (Pericrocotus | 1 |Lombok) |Oriental genus 48. Graucalus | 20 |Celebes to New Hebrides|Oriental | | and N. Zealand | 49. _Artamides_ | 1 |Celebes | 50. _Pteropodocys_ | 1 |Australia | 51. Campephaga | 12 |Celebes to Timor & |Oriental, Ethiopian | | New Guinea | 52. Lalage | 15 |Celebes to Australia & |Malayan | | Samoan Ids. | 53. _Symmorphus_ | 1 |E. Australia and | | | Norfolk Id. | | | | DICRURIDÆ. | | | | | | 54. Dicrurus | 11 |Celebes to N. Ireland &|Oriental, Ethiopian | | Austral. | 55. _Chætorhynchus_| 1 |New Guinea | | | | MUSCICAPIDÆ. | | | | | | 56. _Peltops_ | 1 |Papuan Islands | 57. _Monarcha_ | 30 |The whole region (excl.| | |Celebes and N. Zealand)| 58. _Leucophantes_ | |N. Guinea | (Butalis | 1 |Moluccas and Celebes) |Palæarc., Orien., | | | Ethiop. 59. _Micræca_ | 6 |Timor, N. Guinea, | | | Australia | 60. Cyornis | 2 |Celebes and Timor |Oriental 61. Siphia | 1 |Timor |Oriental 62. _Seisura_ | 5 |Moluccas to N. Ireland,| | | Austral. | 63. _Myiagra_ | 15 |Moluccas to Samoan Ids.| | | Austral. | (Hypothymis | 2 |Celebes) |Oriental 64._Machærirhynchus_ 4 |Papuan Ids. and | | | N. Australia | 65. Rhipidura | 32 |The region to Samoan |Oriental | | Ids. and N. Zealand | (Myialestes | 1 |Celebes) |Oriental genus (Tchitrea | 1 |Flores) |Orien. & Ethiop. | | | genus 66. _Todopsis_ | 5 |Papuan Islands | 67. _Chasiempis_ | 2 |Sandwich Islands | | | | PACHYCEPHALIDÆ. | | | | | | 68. _Oreoeca_ | 1 |Temperate Australia | 69. _Falcunculus_ | 2 |Temperate Australia | 70. _Pachycephala_ | 45 |Moluccas to Tonga Ids. | | | and Tasmania | 71. Hylocharis | 2 |Celebes and Timor |Oriental 72. _Eopsaltria_ | 10 |Australia to New | | | Hebrides | | | | LANIIDÆ. | | | | | | 73. _Colluricincla_| 4 |Australia and Tasmania | 74. _Rectes_ | 18 |Papuan to Fiji Ids., | | | N. Austral. | (Lanius | 1 |Lombok) |Northern Hemisphere | | | CORVIDÆ. | | | | | | 75. _Strepera_ | 4 |Australia and Tasmania | 76. _Barita_ | 3 |Australia and Tasmania | 77. _Cracticus_ | 9 |Papuan Ids. to Tasmania| 78. _Grallina_ | 1 |Australia | 79. _Streptocitta_ | 2 |Celebes | 80. _Charitornis_ | 1 |Sulla Islands (Celebes | | | group) | 81. Corvus | 8 |The whole region, excl.|Almost Cosmopolite | | N. Zeal. | 82. _Gymnocorvus_ | 2 |Papuan Islands | 83. _Corcorax_ | 1 |Australia | 84. _Lycocorax_ | 3 |Moluccas | | | | PARADISEIDÆ. | | | | | | 85. _Paradisea_ | 4 |Papuan Islands | 86. _Manucodia_ | 3 |Papuan Ids. and | | | N. Australia | 87. _Astrapia_ | 1 |New Guinea | 88. _Parotia_ | 1 |New Guinea | 89. _Lophorina_ | 1 |New Guinea | 90. _Diphyllodes_ | 3 |Papuan Islands | 91. _Xanthomelus_ | 1 |New Guinea | 92. _Cicinnurus_ | 1 |Papuan Islands | 93. _Paradigalla_ | 1 |New Guinea | 94. _Semioptera_ | 1 |Gilolo and Batchian | 95. _Epimachus_ | 1 |New Guinea | 96. _Drepanornis_ | 1 |New Guinea | 97. _Seleucides_ | 1 |New Guinea | 98. _Ptilorhis_ | 4 |New Guinea and | | | N. Australia | 99. _Sericulus_ | 1 |E. Australia | 100. _Ptilorhynchus_| 1 |E. Australia | 101. _Chlamydodera_ | 4 |N. and E. Australia | 102. _Æluredus_ | 3 |Papuan Islands and | | | E. Australia | 103. _Amblyornis_ | 1 |New Guinea | | | | MELIPHAGIDÆ. | | | | | | 104. _Myzomela_ | 20 |The region; excl. | | | N. Zealand | 105. _Entomophila_ | 4 |Papuan Islands and | | | Australia | 106. _Gliciphila_ | 10 |Papuan Ids. Timor, | | |Australia, N. Caledonia| 107._Acanthorhynchus_ 2 |Australia and Tasmania | 108. _Meliphaga_ | 1 |East and S. Australia | 109. _Ptilotis_ | 43 |Lombok and Gilolo to |(Baly) | | Tasmania and | | | Samoan Ids. | 110. _Meliornis_ | 5 |Australia and Tasmania | 111. _Prosthemadera_| 1 |New Zealand | 112. _Anthornis_ | 4 |New Zealand and | | | Chatham Ids. | 113. _Anthochæra_ | 10 |New Guinea to Tasmania | | | and Samoan Ids., | | | N. Zealand | 114. _Pogonornis_ | 1 |New Zealand | 115. _Philemon_ | 18 |Lombok to N. Guinea, | | | N. Caledonia, | | |Australia | 116. _Enicmiza_ | 2 |Australia | 117. _Manorhina_ | 5 |Australia and Tasmania | 118. _Melithreptus_ | 8 |N. Guinea, Australia, | | | Tasmania | 119. _Euthyrhynchus_| 3 |N. Guinea | 120._Melirrhophetes_| 2 |N. Guinea | 121. _Melidectes_ | 1 |N. Guinea | 122. _Melipotes_ | 1 |N. Guinea | 123. _Moho_ | 3 |Sandwich Islands | 124. _Chætoptila_ | 1 |Sandwich Islands | | | | NECTARINIIDÆ. | | | | | | 125. _Cosmetira_ | 1 |Papuan Islands | (Æthopyga | 1 |N. Celebes) |Oriental genus 126. Chalcostetha | 5 |Celebes, Moluccas, |Malaya | | Papuan Ids. | 127. Arachnecthra | 5 |Austro-Malaya and |Oriental | | N. Australia | (Nectarophila | 1 |Celebes) |Oriental genus Anthreptes | 1 |Celebes and Sulla |Malayan genus | | Islands | 128. Arachnothera | 1 |Papuan Islands, Lombok |Oriental | | | DICÆIDÆ. | | | | | | 129. Zosterops | 28 |The region to Fiji Ids.|Oriental, Ethiopian | | & N. Zeal. | 130. Dicæum | 12 |Celebes to Solomon Ids.|Oriental | | & Austral. | 131. Pachyglossa ? | 1 |N. Celebes |Himalayas 132. Piprisoma | 1 |Timor |India, Ceylon 133. _Pardalotus_ | 1 |Australia and Tasmania,| | | Timor | 134. Prionochilus | |Papuan Islands |Malaya | | | DREPANIDIDÆ. | | | | | | 135. _Drepanis_ | 3 |Sandwich Islands | 136. _Hemignathus_ | 3 |Sandwich Islands | 137. _Loxops_ | 1 |Sandwich Islands | 138. _Psittirostra_ | 1 |Sandwich Islands | | | | HIRUNDINIDÆ. | | | | | | 139. Hirundo | 7 |The whole region |Cosmopolite 140. Atticora | 1 |Australia |Neotropical | | | PLOCEIDÆ. | | | | | | 141. Estrilda | 4 |Flores, Timor, |Oriental, Ethiopian | | Australia | 142. _Emblema_ | 1 |N. W. Australia | 143. Munia | 6 |Celebes to N. Guinea |Oriental | | and N. Australia | 144. _Donacola_ | 3 |Australia | 145. _Poephila_ | 6 |Australia | 146. Amadina | 9 |Flores to Tasmania and |Ethiopian | | Samoan Islands | 147. Erythrura | 7 |Moluccas to Caroline |Java, Sumatra | | and Fiji Islands, | | | Timor, N. Caledonia | | | | STURNIDÆ. | | | | | | 148. Eulabes | 4 |Sumbawa, Flores, Papuan|Oriental | | and Solomon Islands | 149. _Basilornis_ | 2 |Celebes and Ceram | (Acridotheres | 1 |Celebes) |Oriental genus 150. _Creadion_ | 2 |N. Zealand | 151. _Heterolocha_ | 1 |N. Zealand | 152. _Callæas_ | 2 |N. Zealand | 153. _Aplonis_ | 8 |N. Caledonia to Tonga | | | Islands | 154. Calornis | 13 |Celebes to Solomon |Malaya | | Islands and | | | N. Australia | 155. _Enodes_ | 1 |Celebes | 156. _Scissirostrum_| 1 |Celebes | | | | ARTAMIDÆ. | | | | | | 157. Artamus | 15 |Celebes to Fiji Ids. |Oriental | | and Tasmania | | | | ALAUDIDÆ. | | | | | | 158. Mirafra | 2 |Flores and Australia |Oriental, Ethiopian | | | MOTACILLIDÆ. | | | | | | 159. Budytes | 11 |Moluccas, Timor, |Palc., Ethiopian, x | | Australia | Australia 160. Corydalla | 5 |Lombok and Moluccas to |Palæarctic, Oriental | | N. Zealand | | | | PITTIDÆ. | | | | | | 161. Pitta | 12 |Celebes and Lombok to |Oriental | |N. Guinea and Australia| 162. Hydrornis | 1 |Gilolo, Batchian |Himalayas to Java 163. _Melampitta_ | 1 |N. Guinea | | | | MENURIDÆ. | | | | | | 164. _Menura_ | 2 |E. Australia | | | | ATRICHIIDÆ. | | | | | | 165. _Atrichia_ | 2 |W. Australia and | | | Queensland | | | | PICARIÆ. | | | PICIDÆ. | | | | | | 166. Yungipicus | 2 |Celebes, Lombok, and |Oriental | | Flores | (Mulleripicus | 1 |Celebes) |Oriental genus | | | CUCULIDÆ. | | | | | | 167. _Rhamphococcyx_| 1 |Celebes | 168. Centropus | 13 |Austro-Malaya and |Oriental, Ethiopian | | Australia | 169. Cuculus | 5 |Austro-Malaya and |Palc., Orien., | | Australia | Ethiopian 170. _Caliechthrus_ | 1 |Papuan Islands | 171. Cacomantis | 10 |Austro-Malaya and |Oriental | | Australia | 172. Chrysococcyx | 5 |Austro-Malaya to Fiji |Oriental, Ethiopian | | Islands and N. Zealand| (Hierococcyx | 1 |Celebes) |Oriental genus 173. Eudynamis | 6 |The whole region; excl.|Oriental | | Sandwich Islands | 174. _Scythrops_ | 1 |Celebes, Moluccas, and | | | Australia | | | | CORACIIDÆ. | | | | | | (Coracias | 1 |Celebes) |Oriental and Ethiopian 175. Eurystomus | 4 |Austro-Malaya and |Oriental and Ethiopian | | Australia | | | | MEROPIDÆ. | | | | | | 176. _Meropogon_ | 1 |Celebes | 177. Merops | 2 |Austro-Malaya and |Palc., Orien., | | Australia | Ethiopian | | | ALCEDINIDÆ. | | | | | | 178. Alcedo | 4 |Celebes to New Ireland |Palc., Orien., | | | Ethiopian 179. _Alcyone_ | 6 |Batchian to Tasmania |Philippines 180. Pelargopsis | 2 |Celebes, Flores |Oriental 181. Ceyx | 7 |Celebes to New Guinea |Oriental 182. _Ceycopsis_ | 1 |Celebes | 183. _Syma_ | 2 |Papuan Islands and | | | N. Australia | 184. Halcyon | 19 |The whole region; excl.|Oriental, Ethiopian | | Sandwich Islands | 185. _Todirhamphus_ | 3 |Central Pacific and | | | Sandwich Ids. | 186. _Dacelo_ | 6 |Papuan Islands and | | | Australia | 187. _Monachalcyon_ | 1 |Celebes | 188. _Caridonax_ | 1 |Lombok and Flores | 189. _Tanysiptera_ | 14 |Batchian to N. Guinea | | | and N. Australia | 190. _Cittura_ | 2 |Celebes and Sanguir | | | Islands | 191. _Melidora_ | 1 |New Guinea | | | | BUCEROTIDÆ. | | | | | | 192. Hydrocissa? | 1 |Celebes |Oriental 193. Calao | 1 |Moluccas to Solomon |Malayan | | Islands | 194. Cranorrhinus? | 1 |Celebes |Malayan | | | PODARGIDÆ. | | | | | | 195. _Podargus_ | 10 |Papuan Islands to | | | Tasmania | 196. Batrachostomus | 2 |Moluccas |Oriental 197. _Ægotheles_ | 5 |Papuan Islands to | | | Tasmania | | | | CAPRIMULGIDÆ. | | | | | | 198. Caprimulgus | 4 |Lombok to Australia, |Palc., Ethiopian, | | N. Guinea to Pelew | Orien. | | Islands | 199. _Eurostopodus_ | 2 |Aru Islands and |Oriental genus | | Australia | (Lyncornis | 1 |Celebes) | | | | CYPSELIDÆ. | | | | | | 200. Dendrochelidon | 2 |Celebes to N. Guinea |Oriental 201. Collocalia | 4 |Celebes to Pacific |Oriental | | Islands | 202. Cypselus | 1 |Australia |Palc., Orien., | | | Ethiopian 203. Chætura | 2 |Celebes, Australia |Ethio., Orien., | | | American | | | PSITTACI. | | | CACATUIDÆ. | | | | | | 204. _Cacatua_ | 17 |Celebes and Lombok, to |Philippines | | Solomon Islands and | | | Tasmania | 205. _Calopsitta_ | 1 |Australia | 206._Calyptorhynchus_ 8 |Australia and Tasmania | 207. _Microglossus_ | 2 |Papuan Islands and | | | N. Austral. | 208. _Licmetis_ | 3 |Austr., Solmn. Ids., & | | | N. Guin. ? | 209. _Nasiterna_ | 3 |Papuan and Solomon | | | Islands | | | | PLATYCERCIDÆ. | | | | | | 210. _Platycercus_ | 14 |Austral., Tasmania, | | | Norfolk Id. | 211. _Psephotus_ | 6 |Australia | 212. _Polytelis_ | 3 |Australia | 213. _Nymphicus_ | 1 |Australia and | | | N. Caledonia | 214. _Aprosmictus_ | 6 |Moluccas, Timor, Papuan| | | Islands, Australia | 215. _Pyrrhulopsis_ | 3 |Tonga to Fiji Islands | 216. _Cyanoramphus_ | 14 |N. Zealand, Norfolk | | | Island, N. Caledonia,| | | Society Islands | 217. _Melopsittacus_| 1 |Australia | 218. _Euphema_ | 7 |Australia | 219. _Pezoporus_ | 1 |Australia and Tasmania | 220. _Geopsittacus_ | 1 |W. Australia | | | | PALÆORNITHIDÆ. | | | | | | 221. _Prioniturus_ | 2 |Celebes |Philippines 222. _Geoffroyus_ | 5 |Borneo to Timor & | | | Solomon Ids. | 223. _Tanygnathus_ | 4 |Celebes to New Guinea |Philippines 224. _Eclectus_ | 8 |Moluccas and Papuan | | | Islands | 225. _Cyclopsitta_ | 7 |Papuan Ids. and N. E. |Philippines | | Austral. | 226. Loriculus | 7 |Celebes to Mysol, |Oriental | | Flores | 227. _Trichoglossus_| 29 |The whole region, excl.| | | Sandwich Islands, and| | | N. Zealand | 228. _Nanodes_ | 1 |Australia and Tasmania | 229. _Charmosyna_ | 1 |New Guinea | 230. _Eos_ | 9 |Sanguir Ids. and | | | Moluccas to | | | Solomon Ids. | 231. _Lorius_ | 23 |Bouru and Gilolo to | | | Solomon Ids. | 232. _Coriphilus_ | 4 |Samoan to Marquesas | | | Islands | | | | NESTORIDÆ. | | | | | | 233. _Nestor_ | 5 |New Zealand and | | | Norfolk Ids. | 234. _Dasyptilus_ | 1 |New Guinea | | | | STRINGOPIDÆ. | | | | | | 235. _Stringops_ | 1 |N. Zealand, Chatham | | | Islands? | | | | COLUMBÆ. | | | COLUMBIDÆ. | | | | | | 236. Treron | 5 |Celebes, Bouru, and |Oriental, Ethiopian | |Ceram, Flores and Timor| 237. Ptilopus | 50 |The whole region; excl.|Indo-Malaya | | N. Zealand | 238. Carpophaga | 40 |The whole region |Oriental 239. Ianthænas | 6 |Gilolo, Timor, Papuan |Japan, Philippines, | | Ids. to Samoan Islands| Andaman Islands 240. _Leucomeloena_ | 1 |Australia | 241. _Lopholæmus_ | 1 |Australia | 242. Geopelia | 5 |Lombok to Tasmania |Malaya, China 243. Macropygia | 6 |Austro-Malaya, |Indo-Malaya | | Australia | 244. _Turacoena_ | 3 |Celebes, Timor, Solomon| | | Ids. | 245._Reinwardtoenas_| 1 |Celebes to New Guinea | 246. Turtur | 2 |Austro-Malaya |Palæarc., Orien., | | | Ethiop. 247. _Ocyphaps_ | 1 |Australia | 248. _Petrophassa_ | 1 |N. W. Australia | 249. Chalcophaps | 4 |Austro-Malaya, |Oriental | | Australia | 250. _Trugon_ | 1 |N. Guinea | 251. _Henicophaps_ | 1 |Papuan Islands | 252. _Phaps_ | 3 |Australia and Tasmania | 253. _Leucosarcia_ | 1 |Australia | 254. _Geophaps_ | 2 |Australia | 255. _Lophophaps_ | 3 |Australia | 256. _Caloenas_ | 1 |Austro-Malaya |Indo-Malaya 257. _Otidiphaps_ | 1 |N. Guinea | 258. Phlogoenas | 7 |Celebes, N. Guinea to |Philippine Islands | | Madagascar | 259. _Goura_ | 3 |Papuan Islands | | | | DIDUNCULIDÆ. | | | | | | 260. _Didunculus_ | 1 |Samoan Islands | | | | GALLINÆ. | | | | | | TETRAONIDÆ. | | | | | | 261. _Coturnix_ | 9 |Celebes, Timor, |Palæarc., Orien., | | Australia, N. Zealand| Ethiop. | | | PHASIANIDÆ. | | | | | | (Gallus | 2 |Celebes to Timor) |Oriental genus | | | TURNICIDÆ. | | | | | | 262. Turnix | 9 |Celebes & Moluccas to |Palæarc., Orien., | | Tasmania | Ethiop. | | | MEGAPODIIDÆ. | | | | | | 263. _Talegallus_ | 3 |Papuan Islands and | | | Australia | 264. _Megacephalon_ | 1 |Celebes | 265. _Lipoa_ | 1 |S. Australia | 266. _Megapodius_ | 12 |Celebes to Austral. & |Philippines, | | Samoan Ids. | Nicobar Ids. | | | ACCIPITRES. | | | FALCONIDÆ. | | | | | | 267. Circus | 2 |Celebes, S. and E. |Almost Cosmopolite | | Austral | 265. Astur | 20 |The region, to Fiji |Almost Cosmopolite | | Islands | 269. Accipiter | 6 |The whole region, to |Almost Cosmopolite | | Fiji Islands | 270. _Urospiza_ | 1 |Australia | 271. _Uroaëtus_ | 1 |Australia and Tasmania | 272. Nisaëtus | 1 |Australia |S. Palæarc., | | | Ethiopian, Oriental 273. Neopus | 1 |Celebes and Ternate |Oriental 274. Spizaëtus | 2 |Celebes and N. Guinea |Neotrop., Ethiop., | | | Orien. 275. Circaëtus | 1 |Timor and Flores |Palæarc., Ethiop., | | | Orien. (Spilornis | 2 |Celebes and Sulla |Oriental genus | | Islands) | 276. Butastur | 1 |Celebes to New Guinea |Oriental, N. E. Africa 277. Haliæetus | 1 |The whole region |Cosmop., excl. | | | Neotrop. region 278. Haliastur | 2 |Australia and |Oriental | | N. Caledonia | 279. Milvus | 1 |Celebes to Australia |Palæarc., Orien., | | | Ethiop. 280. _Lophoictinia_ | 1 |Australia | 281. _Gypoictinia_ | 1 |Australia | 282. Elanus | 3 |Celebes and Australia |Oriental, Ethiopian 283. _Henicopernis_ | 1 |Papuan Islands | (Pernis | 1 |Celebes) |Palæarctic, Oriental, | | | and Ethiopian 284. Baza | 4 |Moluccas and Australia |Oriental 285. _Harpa_ | 1 |N. Zealand and | | | Auckland Ids. | 286. Falco | 6 |Austro-Malaya and |Almost Cosmopolite | | Australia | 287. _Hieracidea_ | 2 |Australia and Tasmania | 288. Cerchneis | 2 |Austro-Malaya and |Almost Cosmopolite | | Australia | | | | PANDIONIDÆ. | | | | | | 289. Pandion | 1 |The whole region |Cosmopolite 290. Polioaëtus | 1 |Celebes and Sandwich |Oriental | | Islands | | | | STRIGIDÆ. | | | | | | 291. Athene | 21 |The whole reg., excl. |Palæarc., Orien., | | Pacific Ids. | Ethiop. 292. Scops | 6 |Celebes, Moluccas, |Almost Cosmopolite | | N. Zealand | (Asio | 1 |Sandwich Islands) |Almost Cosmopolite, | | | excl. Australian | | | region 293. Strix | 7 |The whole region |Cosmopolite _Peculiar or very Characteristic Genera of Wading and Swimming Birds._ GRALLÆ. | | | RALLIDÆ. | | | | | | _Ocydromus_ | 5 |New Zealand | _Cabalus_ | 1 |Chatham Islands | _Notornis_ | 2 |New Zealand, Norfolk | | |and Lord Howe's Islands| _Tribonyx_ | 4 |Australia and | | | N. Zealand | _Habroptila_ | 1 |Moluccas | Rallina | 6 |Austro-Malaya |Oriental _Pareudiastes_ | 1 |Samoan Islands | | | | SCOLOPACIDÆ. | | | | | | _Cladorhynchus_ | 1 |Australia | | | | CHARADRIIDÆ. | | | | | | Esacus | 1 |Austro-Malaya, |Oriental | | Australia | _Erythrogonys_ | 1 |Australia | _Thinornis_ | 2 |New Zealand | _Anarhynchus_ | 1 |New Zealand | _Pedionomus_ | 1 |Australia | | | | RHINOCHETIDÆ. | | | | | | _Rhinochetus_ | 1 |New Caledonia | | | | ANATIDÆ. | | | | | | _Nesonetta_ | 1 |Auckland Islands | _Malacorhynchus_| 1 |Australia | _Hymenolæmus_ | 1 |New Zealand | _Biziura_ | 1 |Australia | _Anseranas_ | 1 |Australia | _Cereopsis_ | 1 |Australia and Tasmania | | | | PROCELLARIIDÆ. | | | | | | Prion | 6 |New Zealand |Antarctic Seas | | | SPHENISCIDÆ. | | | | | | Eudyptes | 4 |Australia and |Antarctic shores | | N. Zealand | | | | STRUTHIONES. | | | CASUARIIDÆ. | | | | | | 294. _Dromæus_ | 2 |Australia | 295. _Casuarius_ | 9 |Ceram to New Britain, | | | N. Austrl. | | | | APTERYGIDÆ. | | | | | | 296. _Apteryx_ | 4 |New Zealand | | | | DINORNITHIDÆ. | |(Extinct) | | | | 297. _Dinornis_ | 5 |N. Zealand | 298. _Mionornis_ | 2 |N. Zealand | | | | PALAPTERYGIDÆ. | |(Extinct) | | | | 299. _Palapteryx_ | 2 |N. Zealand | 300. _Euryapteryx_ | 2 |N. Zealand | {489}INDEX TO VOL. I. NOTE.--In this Index the names in Italics all refer to fossil genera or families mentioned in Part II. The systematic names of genera and families occurring in almost every page of Part III. are not given, as they would unnecessarily swell the Index; but they can be readily referred to by the Class or Order, or by the Geographical Division (Region or Sub-region) under which they occur. They will, however, all be found in the General Index, with a reference to the page (in Vol. II., Part IV.) where a systematic account of their distribution is given. A. Aardvark of East Africa, figure of, 261 _Accipitres_, European Eocene, 163 Accipitres, classification of, 97 range of Palæarctic genera of, 248 range of Ethiopian genera of, 312 range of Oriental genera of, 385 range of Australian genera of, 484 _Acerotherium_, European Miocene, 119 N. American Tertiary, 136 _Achænodon_, N. American Tertiary, 138 _Acotherium_, European Eocene, 126 _Adapis_, European Eocene, 125 _Ælurogale_, European Eocene, 125 _Æpyornis_, of Madagascar, 164 _Æshna_, from the Lias, 167 _Agnopterus_, European Eocene, 163 _Agriochoerus_, N. American Tertiary, 138 _Agrion_, from the Lias, 167 _Alcephalus_, Indian Miocene, 122 Aldabra Islands, land-tortoises of, 289 _Aletornis_, N. American Eocene, 163 Algeria, Post-Pliocene deposits and caves of, 111 Allen, Mr. J. A., on Zoological regions, 61 objections to his system of circumpolar zones, 67 objections to his zoo-geographical nomenclature, 68 Altai mountains, fossils in caves, 111 _Amblyrhiza_, Pliocene of Antilles, 148 America, recent separation of North and South, 40 extinct mammalia of, 129 North, Post-Pliocene fauna of, 129 _Amomys_, N. American Tertiary, 134 _Amphechinus_, European Miocene, 117 Amphibia, means of dispersal of, 28 classification of, 100 peculiar to Palæarctic region, 186 of Central Europe, 196 of the Mediterranean sub-region, 205 of Siberian sub-region, 220 Amphibia, of the Manchurian sub-region, 226 table of Palæarctic families of, 237 of the Ethiopian region, 255 of West Africa, 264 South African, 268 of Madagascar, 280 table of Ethiopian families of, 298 of the Oriental region, 317 of the Indian sub-region, 326 of Ceylon, 327 of Indo-Chinese sub-region, 331 of Indo-Malay sub-region, 340 table of Oriental families of, 369 of the Australian region, 397 resemblances of Australian and South-American, 400 of New Guinea, 416 of New Zealand, 457 _Amphibos_, Indian Miocene, 122 _Amphicyon_, European Miocene, 118 Indian Miocene, 121 N. American Tertiary, 134 _Amphimericidæ_, European Miocene, 119 _Amphimoschus_, European Miocene, 120 _Amphisorex_, European Miocene, 118 _Amphitragulus_, European Miocene, 120 _Anastoma_, European Tertiary, 169 _Anchilophus_, European Eocene, 125 _Anchippodus_, N. American Eocene, 139 _Anchippus_, N. American Tertiary, 135 _Anchitheridæ_, N. American Tertiary, 135 _Anchitherium_, European Miocene, 119 European Eocene, 125 N. American Tertiary, 135 Ancient fauna of New Zealand, 459 _Ancylotherium_, Miocene of Greece, 116 European Miocene, 121 Andaman Islands, zoology of, 333 probable past history of, 334 _Andreas_, European Miocene, 165 Animal kingdom, primary divisions of, 85 Animals, development of, affecting distribution, 7 dispersal and migration of, 10 rapid multiplication of, 10 {490} _Anisacodon_, N. American Tertiary, 137 Anoa of Celebes, peculiarities of, 428 _Anoplotheriidæ_, European Miocene, 119 _Anoplotherium_, European Miocene, 119 European Eocene, 126 S. American Eocene, 148 Anseres, arrangement of, 98 peculiar Palæarctic genera, 250 peculiar Ethiopian genera of, 313 peculiar Australian genera of, 485 Antelopes in the Indian Miocene deposits, 122 birthplace and migrations of, 155 Palæarctic, 182 _Antelotherium_, Indian Miocene, 122 _Anthracotheridæ_, N. American Tertiary, 137 _Anthracotherium_, European Miocene, 110 _Antiacodon_, N. American Tertiary, 133 Antilles, Pliocene Mammalia of, 148 _Antilope_, Post-Pliocene, 112 in Brazilian caves, 144 Antiquity of the genera of insects, 166 of the genera of land and freshwater shells, 168 _Aphanapteryx_ of Mauritius, 164 _Aphelotherium_, European Eocene, 125 _Aquila_, European Miocene, 161 _Archæopteryx_, Bavarian Oolite, 163 Arctic zone not a separate region, 68 _Arctocyon_, European Eocene, 125 _Arctodus_, N. American Post-Pliocene, 130 _Arctomys_, European Pliocene, 113 _Arctotherium_ in Brazilian caves, 144 S. American Pliocene, 146 Argus pheasant, figure of, 339 peculiarity, in display of plumage, and confirmation of Mr. Darwin's views, 340 _Artiodactyla_, European Eocene, 126 N. American Tertiary, 137 S. American Pliocene, 146 _Arvicola_, European Pliocene, 113 in Brazilian caves, 145 S. American Pliocene, 147 S. American Eocene, 148 _Auchena_, N. American Post-Pliocene, 130 Auckland Islands, birds of, 455 Australia, physical features of, 387 Australia and S. America, supposed land connection between, 398 Australian region, description of, 387 zoological characteristics of, 390 mammalia of, 390 birds of, 391 reptiles of, 396 amphibia of, 397 fresh-water fish of, 397 summary of vertebrata of, 397 supposed land-connection of with S. America, 398 insects of, 403 lepidoptera of, 404 coleoptera of, 405 land shells of, 407 sub-regions of, 408 early history of, 465 Australian sub-region, mammalia of, 438 illustration of mammalia of, 439 birds of, 440 illustration of fauna of, 441 Austro-Malayan sub-region, physical features of, 388 zoology of, 409 Aye-aye, figure of, 278 Azores, visited by European birds, 17 birds of, 207 butterflies of, 207 beetles of, 207, 209 peculiarly modified birds of, 207 stragglers to, 208 how stocked with animal life, 208 B. Babirusa of Celebes, peculiarities of, 428 Badger, figure of, 195 _Balæna_, European Pliocene, 112 _Balænodon_, European Pliocene, 112 Baly, Mr., on Phytophaga of Japan, 230 Banca, its peculiar species and solution of a problem in distribution, 356 Barriers, as affecting distribution, 6 permanence of, as affecting distribution, 7 to the dispersal of birds, 17 Bates, Mr., on Carabidæ of Japan, 228 on Longicorns of Japan, 230 _Bathmodon_, N. American Tertiary, 136 _Bathrodon_, N. American Tertiary, 133 _Batrachia_, Tertiary, 165 Bats, powers of flight of, 15 classification of, 87 of New Zealand, 450 Bears, probable cause of absence of, from tropical Africa, 291 Beaver, N. American Tertiary, 140 Beetles, families selected for study, 103 from the Lias, 167 of Azores, 207 of Japan, 228 _Belemnoziphius_, European Pliocene, 112 Belt, Mr., his theory of a great Siberian lake during the glacial epoch, 218 on change of climate caused by diminution of obliquity of ecliptic, 466 Birds, means of dispersal of, 15 dispersal of by winds, 16 American, found in Europe, 16 reaching the Azores, 17 barriers to dispersal of, 17 limited by forests, 17 classification of, 93 Miocene of Greece, 116 extinct, 160 fossil of Palæarctic region, 161 European of Miocene period, 161 Eocene of Europe, 162 relations of, 162 extinct of North America, 163 recently extinct in New Zealand, 164 Cretaceous of N. America, 164 remains of in Brazilian caves, 164 recently extinct in Madagascar and the Mascarene Islands, 164 cosmopolitan groups of, 176 numerous genera, Palæarctic, 183 of the European sub-region, 193 northern range of in Europe, 193 of the zone of pine forests, 194 of Iceland, 198 of the Mediterranean sub-region, 203 of Malta, 206 (_note_) of Azores, 207 of the Cape Verd Islands, 215 of Siberian sub-region, 219 Oriental found in Siberia, 219 extreme northern Asiatic, 219 of northern Asiatic forests, 220 of the Manchurian sub-region, 223 Palæarctic genera of, in the Manchurian sub-region, 224 Oriental genera of, in the Manchurian sub-region, 224 {491} characteristic of N. W. China and Mongolia, 226 table of Palæarctic families of, 235 of West Africa, 243 list of Palæarctic genera of, 243 of the Ethiopian region, 253 of the East African sub-region, 260 S. African, 267 genera of, peculiar to Madagascar, 275 common to Madagascar and Oriental or Ethiopian regions, 276 species common to Madagascar and Africa or Asia, 277 table of Ethiopian families of, 295 table of Ethiopian genera of, 306 of the Oriental region, 316 of the Indian sub-region, 323 Oriental genera of in Central India, 324 Palæarctic and Ethiopian genera in Central India, 325 of Ceylon, 327 of Indo-Chinese sub-region, 330 of Indo-Malayan sub-region, 337 illustration of peculiar Malayan, 339 of the Philippine Islands, 346 table of Oriental families of, 366 table of Oriental genera of, 375 of Australian region, 391 specially organized Australian families of, 392 of the Papuan Islands, 410 peculiarities of, 413 brilliant colours of, 413 remarkable forms of, 414 of the Moluccas, 418 peculiarities of, 421 of Timor group, 423 of Celebes, 428 of Australia, 440 of New Zealand, 451 peculiar to New Zealand, 452 of Norfolk Island, 453 of Lord Howe's Island, 453 of the Chatham Islands, 454 of the Auckland Islands, 455 table of families of Australian, 471 table of genera of Australian, 478 Black ape of Celebes, 427 Blanford, Mr. W. T., on the "Indian" region, 60 on relations of Indian sub-region with Africa, 321 _Blapsidium_, Oolitic insect, 167 Blyth, Mr., on zoological regions, 60 on the relations of Indian sub-region with Africa, 321 Borneo, probable recent changes in, 357 _Bos_, Post-Pliocene, 112 Indian Miocene, 122 Bourbon, zoology of, 280 reptiles of, 281 _Bovidæ_, European Miocene, 120 _Brachymys_, European Miocene, 120 _Bramatherium_, Miocene of Perim Island, 122 Brazilian cave-fauna, 143 remarks on, 145 _Breyeria borinensis_, carboniferous insect, 168 Britain, peculiar species in, 197 British Isles, zoology of, 197 Broad-bill, Malayan, figure of, 340 _Brontotheridæ_, N. American Tertiary, 137 _Brontotherium_, N. American Tertiary, 137 _Bubo_, European Miocene, 162 _Bulimus_, Eocene, 169 _Bunælurus_, N. American Tertiary, 134 _Buprestidium_, Oolitic insect, 167 Butterflies, arrangement of, 103 Palæarctic, 187 of Central Europe, 196 of the Mediterranean sub-region, 205 of Azores, 207 peculiar to Siberian sub-region, 220 of Japan and North China, 227 of the Ethiopian region, 255 number of Ethiopian species, 256 of Indo-Malay sub-region, 342 of the Australian region, 404 of the Austro-Malay sub-region, 404 of the Moluccas, 419 of Celebes, peculiarities of, 434 of New Zealand, 457 C. _Cadurcotherium_, European Eocene, 125 _Cælodon_, in Brazilian caves, 145 _Cælogenys_, in Brazilian caves, 144 _Cænopithecus_, European Eocene, 124 _Cainotherium_, European Miocene, 120 European Eocene, 126 _Calamodon_, N. American Eocene, 139 _Callithrix_ in Brazilian caves, 184 Canaries, birds of, 208 beetles of, 209 _Canidæ_, European Miocene, 118 European Eocene, 125 N. American Tertiary, 134 remarkable S. African, 267 _Canis_, European Pliocene, 112 Post-Pliocene, 112 European Miocene, 118 Indian Miocene, 121 European Eocene, 125 N. American Post-Pliocene, 129 N. American Tertiary, 134, 135 in Brazilian caves, 144 S. American Pliocene, 146 Camel, fossil in Indian Miocene, 122 birth-place and migrations of, 155 Palæarctic, 182 _Camelidæ_, essentially extra-tropical, 112 N. American Tertiary, 138 _Camelopardalis_, Miocene of Greece, 116 Indian Miocene, 122 _Camelotherium_, S. American Pliocene, 147 Cape of Good Hope, peculiar flora and of, 266 Cape Verd Islands, zoology of, 214 Cape-hare, S. African, 267 _Cardiodus_, S. American Pliocene, 147 _Cariama_, Brazilian caves, 164 _Carnivora_ of European Pliocene, 112 Miocene of Greece, 115 European Miocene, 118 Indian Miocene, 121 European Eocene, 125 N. American Post-Pliocene, 129 N. American Tertiary, 134 of Brazilian caves, 144 S. American Pliocene, 146 Carnivora, classification of, 88 antiquity of, 153 of the Palæarctic region, 182 list of Palæarctic genera of, 240 list of Ethiopian genera of, 302 range of Oriental genera of, 373 list of Australian genera of, 476 Caroline Islands, birds of, 444 _Carterodon_ in Brazilian caves, 145 Carus, and Gerstaeker on classification of animals, 85 {492} Professor, on classification of the Cetacea, 88 _Castor_, European Pliocene, 113 European Miocene, 120 _Casoryx_, N. American Tertiary, 138 _Cathartes_, Brazilian caves, 164 Cave-fauna of Brazil, 143 _Cavia_, European Miocene, 121 in Brazilian caves, 144 S. American Pliocene, 147 _Cebochoerus_, European Eocene, 126 _Cebus_ in Brazilian caves, 144 Celebes, physical features of, 389 mammalia of, 426 birds of, 428 insects of, 434 origin of fauna of, 436 _Centetidæ_, European Miocene, 118 Ceratodus, remarkable Australian fish, 397 _Cercolabes_ in Brazilian caves, 145 _Cercopithecus_ in European Pliocene, 112 _Cervidæ_, European Miocene, 120 birth-place and migrations of, 155 _Cervus_, European Pliocene, 113 Indian Pliocene and Miocene, 122 N. American Post-Pliocene, 130 N. American Tertiary, 138 in Brazilian caves, 144 S. American Pliocene, 147 _Cetacea_, European Pliocene, 112 European Miocene, 119 N. American Post-Pliocene, 130 N. American Tertiary, 140 Cetacea, classification of, 89 range of Oriental genus, 374 Ceylon and Malaya, resemblance of insects of, 327 Ceylonese sub-region, 326 mammalia of, 327 birds of, 327 reptiles of, 327 amphibia of, 327 insects of, 327 past history of, as indicated by its fauna, 328 _Chalicomys_, European Pliocene, 113 _Chalicotherium_, European Miocene, 119 Indian Miocene, 122 fossil in N. China, 123 _Chamæleo_, N. American Eocene, 165 Chamois, figure of, 195 Chatham Islands, birds of, 454 Chelonia, classification of, 100 _Chelydra_, European Pliocene, 165 Chevrotain of Malaya, figure of, 336 Chili should not be placed in the Palæarctic or Nearctic regions, 63 China, fossil mammals in, resembling those of Indian and European Miocene, 362 North, mammalia of, 222 _Chinchillidæ_ in Brazilian caves, 145 S. American Pliocene, 147 Pliocene of Antilles, 148 Chiroptera, classification of, 87 list of Palæarctic genera of, 239 list of Ethiopian genera of, 300 range of Oriental genera of, 371 list of Australian genera of, 475 _Chiroptera_, European Eocene, 125 in Brazilian caves, 144 _Chlamydotherium_ in Brazilian caves, 145 _Choeromorus_, European Miocene, 119 _Choeropotamus_, European Eocene, 126 _Choerotherium_, Indian Miocene, 122 _Choneziphius_, European Pliocene, 112 Chough, Alpine, figure of, 195 Circumpolar zones, objections to system of, 67 Classification as affecting the study of distribution, 83 _Clausilia_, Eocene, 169 Climate, as a limit to the range of mammalia, 11 gradual change of, before the glacial epoch, 41 Coleoptera, families selected for study, 103 Palæarctic, 188 number of Palæarctic species, 189 of Central Europe, 196 of the Mediterranean sub-region, 205 of the Cape Verd Islands, 215 of the Ethiopian region, 256 S. African, 268 of Madagascar, 282, 283 of the Oriental region, 319 of Indo-Malay sub-region, 342 of the Australian region, 405 affinity of Australian and South American, 406, 407 of Celebes, 435 of New Zealand, 457 _Collocalia_, European Miocene, 161 _Colobus_, European Miocene, 117 _Colonoceras_, N. American Tertiary, 136 _Colossochelys_ of Indian Miocene, 123, 165 Columbæ, classification of, 96 range of Palæarctic genera of, 248 range of Ethiopian genera of, 311 range of Oriental genera of, 384 range of Australian genera of, 485 Comoro islands, zoology of, 281 Continents, distribution of, 37 recent changes of, 38 Continental extension in Mesozoic times, 156 _Corvus_, European Miocene, 161 _Coryphodon_, European Eocene, 126 Cosmopolitan groups enumerated, 175 _Cricetodon_, European Miocene, 120 _Cricetus_, European Pliocene, 113 Crocodiles, Eocene, 165 Crocodilia, classification of, 100 Crook-billed plovers of New Zealand, 456 Crotch, Mr., on beetles of the Azores, 209 Crowned-pigeon, figure of, 415 _Cryptornis_, European Eocene, 163 _Ctenomys_, S. American Pliocene, 147 Cuba, extinct mammalia of, 148 _Curculionidium_, Oolitic insect, 167 _Cyclostoma_, Eocene, 169 _Cyllo sepulta_, European Cretaceous, 167 _Cynælurus_, in Brazilian caves, 144 Cynopithecus of Celebes, affinities of, 427 _Cyotherium_, European Eocene, 125 D. _Daptophilus_, N. American Tertiary, 134 Darwin, Mr., his explanation of the cause of the abundance of apterous insects in Madeira, 211 on the relation of flowers and insects, 463 _Dasyprocta_, European Miocene, 121 in Brazilian caves, 144 _Dasypus_, in Brazilian caves, 145 S. American Pliocene, 147 _Dasyurus_, Australian Post-Tertiary, 157 David, Père, his researches in China and Thibet, 221, 222 on birds of N. China, 226 Deer, fossil in N. American Tertiary formations, 138 {493} Palæarctic, 182 probable cause of absence of from tropical Africa, 291 _Delphinus_, European Pliocene, 112 _Dendrocygna_, European Miocene, 162 Desman of S. Russia, figure of, 219 _Diceratherium_, N. American Tertiary, 137 _Dichobune_, European Eocene, 126 _Dicotyles_, N. American Post-Pliocene, 130 N. American Tertiary, 137 in Brazilian caves, 144 S. American Pliocene, 146 birthplace and migrations of, 155 _Dicrocerus_, European Miocene, 120 _Didelphys_, European Eocene, 126 N. American Post-Pliocene, 130 in Brazilian caves, 145 _Dididæ_, 164 _Dinocerata_, N. American Tertiary, 139 _Dinoceras_, N. American Eocene, 139 _Dinornis_, allied form in European Eocene, 163 of New Zealand and Australia, 164 _Dinornithidæ_ of New Zealand, 164 _Dinotherium_, Miocene of Greece, 116 European Miocene, 120 Miocene of Perim Island, 123 _Dinyctis_, N. American Tertiary, 134 _Dinylus_, European Miocene, 117 _Diplacodon_, N. American Tertiary, 136 _Diprotodon_, Australian Post-Tertiary, 157 Dispersal of animals, 10 of mammalia, 10 of reptiles and amphibia, 28 Distribution, affected by climate, 5 affected by physical features, 5 contrasts of, in similar climates, 5 similarities of, in diverse climates, 6 barriers as affecting, 6 study of, dependent on a good classification, 83 of animals an adjunct to geology, 8 of animals requires certain preliminary studies, 8 of animals dependent on physical geography, 35 of animals, as affected by the glacial epoch, 40 of animals, as affected by changes of vegetation, 43 of animals, as affected by organic changes, 44 of animals, hypothetical illustration of, 46 of animals, complexity of the causes affecting the, 49 of animals, problems in, 51 of plants, as affected by the glacial epoch, 42 Dodo of Mauritius, 282 _Dolichopterus_, European Miocene, 162 _Dommina_, N. American Tertiary, 134 _Dorcatherium_, European Miocene, 120 _Dremotherium_, Miocene of Greece, 116 European Miocene, 120 Dresser, Mr. H. E., on northern range of European birds, 193 _Dromatherium_, N. American Triassic, 134 oldest American mammal, 160 Drongo-shrike, Malayan, figure of, 340 _opithecus_, European Miocene, 117 E. East Africa, geographical features of, 258 wide range of genera and species over, 259 few special types in, 260 East African sub-region, description of, 258 genera and species ranging over the whole of, 259 mammalia of, 260 birds of, 260 reptiles of, 260 amphibia and fishes of, 260 insects of, 260 few peculiar types in, 260 illustration of zoology of, 261 East Australia, peculiar birds of, 440 East Thibet, mammalia of, 222 Eaton, Rev. A. E., on insects of Kerguelen Island, 211 _Echimyidæ_, in Brazilian caves, 145 _Echinogale_, European Miocene, 118 _Ectognathus_, N. American Eocene, 139 _Edentata_, Miocene of Greece, 116 European Miocene, 121 N. American Post-Pliocene, 130 N. American Pliocene, 140 of Brazilian caves, 145 S. American Pliocene, 147 Edentata, classification of, 90 probable birthplace of, 155 range of Ethiopian genera of, 305 range of Oriental genus of, 375 Elephants, fossil of Indian Miocene, 123 fossil in N. American Post-Pliocene formations, 130 birthplace and migrations of, 155 Elephant shrews, S. African, 267 _Elephas_, Post-Pliocene, 112 fossil in N. China, 123 N. American Tertiary, 138 Elliot, Mr., his great work on the birds of paradise, 415 _Elornis_, European Miocene, 162 _Elotherium_, N. American Tertiary, 137, 139 Elwes, Mr., on birds of Persia, 204 on true relations of the birds of Central India, 323 _Embasis_, N. American Tertiary, 134 Emu, figure of, 441 _Emys_, Indian Miocene, 123 Miocene and Eocene, 165 _Emydida_, Indian Miocene, 123 _Enhydrion_, Indian Miocene, 121 _Eobasileus_, N. American Eocene, 139 Eocene period, 124 fauna of S. America, 148 _Ephemera_, from the Lias, 167 _Eporeodon_, N. American Tertiary, 138 _Equidæ_, European Pliocene, 112 Miocene of Greece, 115 European Eocene, 125 _Equus_, European Pliocene, 112 Post-Pliocene, 112 Indian Miocene, 121 N. American Post-Pliocene, 130 N. American Tertiary, 135 Brazilian caves, 144 S. American Pliocene, 146 _Ereptodon_, N. American Post-Pliocene, 130 _Erinaceus_, European Miocene, 117 _Erythromachus_ of Rodriguez, 164 _Esthonyx_, N. American Eocene, 139 Ethiopian region should not include any part of India, 63 defined, 73 subdivisions of, 73 general features of, 251 {494} zoological characteristics of, 252 mammalia of, 253 great speciality of, 253 birds of, 253 reptiles of, 254 amphibia of, 255 fresh-water fish of, 255 summary of vertebrates of, 255 insects of, 255 coleoptera of, 256 terrestrial mollusca of, 257 sub-regions of, 258 Atlantic islands of, 269 the probable past history of, 285 tables of distribution of animals of, 293 _Eumys_, N. American Tertiary, 140 _Euphractus_, S. American Pliocene, 147 Europe, recent changes in physical geography of, 39 Miocene fauna of Central, 117 Miocene fauna of, allied to existing fauna of tropical Asia and Africa, 124 European sub-region, description of, 191 forests of, 192 mammalia of, 192 birds of, 193 reptiles and amphibia of, 195 fresh-water fish of, 196 insects of, 196 islands of, 197 Euryceros of Madagascar, figure of, 278 _Eurydon_, in Brazilian caves, 145 _Eurytherium_, European Eocene, 126 _Eutatus_, S. American Pliocene, 147 _Eutelodon_, European Eocene, 126 _Eutemnodus_, S. American Eocene, 148 Extinct mammalian fauna of Europe, general considerations on, 126 mammalia of N. America and Europe, comparison of, 140 mammalia of the Antilles, 148 mammalia of Old and New Worlds, general remarks on, 148 fauna of New Zealand, 459 Extinction of large animals, causes of, 158 F. Fauna of Japan, general character and affinities of, 230 of Palæarctic region, general conclusions as to, 231 extinct, of Madagascar and Mascarene Islands, 282 Malayan, probable origin of, 359 Moluccan, peculiarities of, 419 Timorese, origin of, 422 of Celebes, origin of, 436 of New Zealand, origin of, 460 _Felis spelæa_, 110 _Felis_, Miocene of Greece, 115 European Miocene, 118 Indian Miocene, 121 N. American Post-Pliocene, 129 in Brazilian caves, 144 Fernando Po, zoological features of, 265 Fiji, Tonga, and Samoa Islands, birds of, 443 Fishes, means of dispersal of, 29 classification of, 101 cosmopolitan groups of, 176 of the Palæarctic region, 186 of the European sub-region, 196 of the Mediterranean sub-region, 205 of the Manchurian sub-region, 227 fresh-water, table of Palæarctic families of, 227 of the Ethiopian region, 255 of South Africa, 268 fresh-water, table of Ethiopian families of, 298 fresh-water, of the Oriental region, 318 of the Indo-Malay sub-region, 341 fresh-water, table of Oriental families of, 369 fresh-water, of the Australian region, 397 fresh-water, resemblance of Australian and S. American, 400 how the transmission may have taken place, 401 fresh-water, of New Zealand, 457 Flamingoes, European Miocene, 162 Flora, of New Zealand, as influenced by scarcity of insects, 462 fossil, of Australia, 467 Flower, Professor, on classification of mammalia, 85 classification of carnivora, 87 Flying Lemur, Malayan, figure of, 337 Flying Opossum, figure of, 442 Formosa, zoology of, 332 Forests, essential to existence of many European animals, 192 Siberian, greatest extent of, 216 G. Galapagos, scarcity of insects in, 463 _Galecynus_, in European Pliocene, 112 _Galera_, N. American Post-Pliocene, 130 _Galeospalax_, European Miocene, 118 _Galeotherium_, Post-Pliocene, 111 _Galethylax_, European Eocene, 125 _Galictis_, in Brazilian caves, 144 Gallinæ, classification of, 96 range of Palæarctic genera of, 248 range of Ethiopian genera of, 311 range of Oriental genera of, 384 range of Australian genera of, 485 _Gallus_, Miocene of Greece, 116 _Gallus bravardi_, European Pliocene, 161 _Gastornis_, European Eocene, 163 Genera common to Post-Pliocene and Pliocene faunas of N. America, 132 Geological history of Oriental region, 362 Gibraltar, cave fauna of, 114 Glacial epoch, as affecting the distribution of animals, 40 as a cause of the great change in the fauna of the temperate zones, since Pliocene times, 151 probably simultaneous in both hemispheres, 151 causing a general subsidence of the ocean, 152 _Glandina_, Eocene, 169 _Glossotherium_, in Brazilian caves, 145 S. American Pliocene, 147 _Glyptodon_, S. American Pliocene, 147 _Gnathopsis_, S. American Pliocene, 147 Goats, Palæarctic, 182 Godman, Mr., on Natural History of the Azores, 207 Golden Moles, S. African, 267 _Graculavus_, N. American Cretaceous, 164 Grallæ, arrangement of, 97 peculiar or characteristic Palæarctic genera, 249 peculiar Ethiopian genera of, 313 peculiar Oriental genera of, 386 {495} peculiar Australian genera of, 484 Gray, Dr. J. E., on classification of Cetacea, 88 Greece, Upper Miocene deposits of, 115 summary of Miocene fauna of, 116 Groups peculiar to a region, how defined, 184 Gulick, Rev. J. T., on Achatinellidæ of the Sandwich Islands, 446 Günther, Dr., his classification of reptiles, 98 his classification of fishes, 101 on gigantic tortoises of Galapagos and the Mascarene Islands, 289 on range of Indian reptiles in the Himalayas, 329 H. Haast, Dr., on extinct birds of New Zealand, 460 Habitat, definition of, 4 Hainan, zoology of, 334 _Halcyornis_, European Eocene, 103 _Halitherium_, European Pliocene, 112 European Miocene, 119 _Helladotherium_, Miocene of Greece, 116 European Miocene, 120 Hatteria of New Zealand, 456 Helictis, Himalayan, figure of, 331 _Helix_, Eocene, 169 _Hemibos_, Indian Miocene, 122 _Hemicyon_, European Miocene, 118 _Herpetotherium_, N. American Tertiary, 134 _Hesperomys_, N. American Tertiary, 140 in Brazilian caves, 145 S. American Pliocene, 147 _Hesperornis_, N. American Cretaceous, 164 _Heterodon_, in Brazilian caves, 145 _Hexaprotodon_, Indian Miocene, 122 Hickman, Mr. John, on a cause of the extinction of large animals, 158 Himalayas, altitude reached by various groups in the, 329, 333 _Hipparion_, European Pliocene, 112 Miocene of Greece, 115 European Miocene, 119 N. American Post-Pliocene, 130 N. American Tertiary, 135 _Hippopotamus_, Post-Pliocene, 112 Europe in Pliocene, 113 Indian Pliocene, 122 _Hipposyus_, N. American Tertiary, 133 _Hippotherium_, European Miocene, 119 Indian Miocene, 122 _Hippotragus_, European Miocene, 120 _Homalodontotherium_, S. American Pliocene, 146 _Homalophus_, European Miocene, 161 _Homocamelus_, N. American Tertiary, 138 Honeysuckers, birds specially adapted to Australia, 392 Hooker, Dr., on deficiency of odours in New Zealand plants, 464 _Hoplocetus_, European Pliocene, 112 _Hoplophoneus_, N. American Tertiary, 134 Horses, fossil, in Indian Miocene, 121 perfect series of ancestral, in N. America, 136 probable birthplace of, 154 Hutton, Capt. F. W., on origin of New Zealand fauna, 461 Huxley, Professor, on zoological regions, 59 division of animal kingdom by, 85 _Hyæna_, Post-Pliocene, 112 Miocene of Greece, 115 European Miocene, 118 Indian Miocene, 121 fossil in N. China, 123 _Hyænarctos_ in European Pliocene, 112 European Miocene, 118 Indian Miocene, 121 S. American Pliocene, 146 _Hyænictis_, Miocene of Greece, 115 European Miocene, 118 _Hyænidæ_, European Miocene, 118 _Hyænodon_, European Miocene, 118 European Eocene, 125 N. American Tertiary, 134 _Hyænodontidæ_, European Miocene, 118 _Hydrochoerus_, N. American Post-Pliocene, 130 _Hydrornis_, European Miocene, 162 _Hyohippus_, N. American Tertiary, 135 _Hyomoschus_, European Miocene, 120 _Hyopotamus_, European Miocene, 119 N. American Tertiary, 137 _Hyopsodus_, N. American Tertiary, 133 _Hyotherium_, European Miocene, 119 _Hypertragulus_, N. American Tertiary, 133 _Hypisodus_, N. American Tertiary, 138 _Hypsiprymnus_, Australian Post-Tertiary, 157 _Hyrachyus_, N. American Tertiary, 136 _Hyracodon_, N. American Tertiary, 136 _Hyracoidea_, classification of, 90 Palæarctic, 242 Ethiopian, 304 _Hyracotherium_, supposed, in European Eocene, 125 European Eocene, 126 _Hystrix_, European Pliocene, 113 Miocene of Greece, 116 N. American Tertiary, 140 I. _Ibidipodia_, European Miocene, 162 Ibidorhynchus, figure of, 331 Iceland, zoology of, 198 _Icthyornis_, N. American Cretaceous, 164 _Icticyon_ in Brazilian caves, 144 _Ictitherium_, Miocene of Greece, 115 European Miocene, 118 _Ictops_, N. American Tertiary, 133 India, Miocene fauna of, allied to that of Europe, 123 geological features of, 328 Indian, sub-region, description of, 321 supposed relation to Ethiopian region, 321 mammalia of, 322 birds of, 323 reptiles and amphibia of, 326 Indo-Chinese, sub-region, description of, 329 zoological characteristics of, 330 illustration of, 331 reptiles of, 331 amphibia of, 331 insects of, 332 islands belonging to, 333 Indo-Malayan sub-region, description of, 334 mammalia of, 336 illustrations of, 336, 339 birds of, 337 remote geographical relations of, 339 reptiles and amphibia of, 340 fishes of, 341 insects of, 341 coleoptera of, 342 terrestrial mollusca of, 343 zoological relations of islands of, 345 recent geographical changes in, 357 probable origin of fauna of, 359 Insects, means of dispersal of, 32 tenacity of life of, 33 {496} adapted to special conditions, 33 groups selected for the study of their geographical distribution, 102 antiquity of the genera of, 166 fossil of European Miocene, 166 European Cretaceous, 167 European Wealden, 167 Palæozoic, 168 Palæarctic, 187 of Central Europe, 196 of the Mediterranean sub-region, 205 of the Siberian sub-region, 220 of the Manchurian sub-region, 227 of the Ethiopian region, 255 of the East African sub-region, 260 of West Africa, 265 S. African, 268 of Madagascar, 282 general remarks on, 284 of tropical Africa and America, probable cause of similarities in, 291 of Indo-Chinese sub-region, 332 of the Oriental region, 318 of Ceylon, 327 of Indo-Malay sub-region, 341 statistics of collecting in the various islands of the Malay Archipelago, 343 of the Australian region, 403 of New Guinea, 417 of the Moluccas, 420 of Timor group, 426 of Celebes, 454 of New Zealand, 458 scarcity of, in New Zealand, 462 influence of, on the flora, 463 _Insectivora_, European Miocene, 117 N. American Post-Pliocene, 129 N. American Tertiary, 133 Insectivora, classification of, 87 of the Palæarctic region, 181 of N. China and E. Thibet, 222 range of Palæarctic genera of, 239 of Madagascar, 273 range of Ethiopian genera of, 301 of the Oriental region, 315 range of Oriental genera of, 372 range of Australian genera of, 476 _Isacis_, N. American Tertiary, 133 _Ischyromys_, N. American Tertiary, 140 Islands, N. European, zoology of, 197 of the Mediterranean sub-region, 206 of the West African sub-region, 265 of Ethiopian region, 269 Mascarene, 280 of the Indo-Chinese sub-region, 333 of Indo-Malay sub-region, 345 Fiji, Tonga, and Samoa, 443 Society and Marquesas, 444 New Caledonia and New Hebrides, 445 Sandwich, 446 of New Zealand sub-region, 453 Norfolk, 453 Lord Howe's, 454 Chatham, 454 Auckland, 455 _Issiodromys_, European Pliocene, 113 J. _Jacchus_, in Brazilian caves, 144 Japan and North China, physical features of, 221 southern extremity of perhaps belongs to the Oriental region, 226 general character of the fauna of, 230 former land-connexions of, 231 Java, mammalia of, 349 productions of, well known, 350 birds of, 351 representative species of birds in, 352 origin of the anomalous features of its fauna, 352 Sumatra and Borneo, their geographical contrasts and zoological peculiarities explained, 357 _Junonia_, European Miocene, 167 K. Kakapoe, of New Zealand, 455 Kangaroos, extinct in Australia, 157 Kerguelen Island, apterous insects of, 211 (_note_) _Kerodon_, in Brazilian caves, 144 S. American Pliocene, 147 King-fisher, racquet tailed, of New Guinea, figure of, 415 Kiwi of New Zealand, 455 Koodoo antelope, figure of, 261 L. Lacertilia, classification of, 99 Ladrone Islands, birds of, 444 _Lagomys_, European Pliocene, 113 European Miocene, 120 _Lagostomus_, in Brazilian caves, 145 S. American Pliocene, 147 Lake Baikal, seals of, 218 Land and water, proportions of, 35 Land and fresh-water shells, antiquity of the genera of, 168 Land-shells, Palæozoic, 169 Palæarctic, 190 of Madeira, 209 of the Cape Verd Islands, 215 of the Ethiopian region, 257 of W. Africa, 265 of Madagascar and the Mascarene Islands, 285 of Indo-Malay sub-region, 344 of the Australian region, 407 of Sandwich Islands, 446 of New Zealand, 459 _Lanius_, European Miocene, 161 _Laopithecus_, N. American Tertiary, 133 _Laornis_, N. American Cretaceous, 164 Lemuria, a hypothetical land, 76 _Lamuravidæ_, 133 _Lemuravus_, N. American Tertiary, 133 _Lemuridæ_, European Eocene, 124 Lemuroidea, range of Ethiopian genera of, 300 range of Oriental genera of, 371 _Lepictis_, N. American Tertiary, 133 Lepidoptera, cosmopolitan families of, 177 table of Palæarctic families of, 238 S. African, 268 table of Ethiopian families of, 299 of the Oriental region, 318 table of Oriental families of, 369 of the Australian region, 404 table of Australian families of, 472 _Leptarchus_, N. American Tertiary, 135 _Leptauchenia_, N. American Tertiary, 138 _Leptochoerus_, N. American Tertiary, 137 _Leptodon_, Miocene of Greece, 116 _Leptomeryx_, N. American Tertiary, 138 _Leptoptilus_, European Miocene, 162 _Leptosomus_, allied form in European Eocene, 168 {497} Leptosomus of Madagascar, 278 figure of, 279 _Leptotherium_, in Brazilian caves, 144 _Lepus_, in Brazilian caves, 145 S. American Pliocene, 147 _Lestodon_, S. American Pliocene, 147 Lewis, Mr. George, his collection of Japan insects, 228 _Lebellula_, from the Lias, 167 Lilljeborg, Professor, on classification of the Rodentia, 90 _Limnæa_, Eocene, 169 European Secondary, 169 _Limnatornis_, European Miocene, 161 _Limnocyon_, N. American Tertiary, 134 _Limnohyus_, N. American Tertiary, 136 _Limnotheridæ_, N. American Tertiary, 133 _Limnotherium_, N. American Tertiary, 133 _Listriodon_, European Miocene, 119 _Lithomys_, European Miocene, 120 _Lithornis_, European Eocene, 163 Lizards, classification of, 99 Tertiary, 165 wide range of a species in Polynesia, 448 _Loncheres_, in Brazilian caves, 145 _Lonchophorus_, in Brazilian caves, 145 _Lophiodon_, European Eocene, 125 N. American Tertiary, 136 _Lophiotherium_, N. American Tertiary, 136 Lord Howe's Island, birds of, 453 _Loxomylus_, Pliocene of Antilles, 148 Lund, Dr., his researches in caves of Brazil, 143 _Lutra_, European Miocene, 118 Indian Miocene, 121 _Lycæna_, Miocene of Greece, 115 Lyre bird, figure of, 441 M. _Macacus_, European Pliocene, 112 Miocene of Greece, 115 Indian Miocene, 121 supposed in European Eocene, 125 _Machairodus_, 110, 111 Miocene of Greece, 115 European Miocene, 118 Indian Miocene, 121 N. American Tertiary, 134 in Brazilian caves, 144 S. American Pliocene, 146 _Macrauchenia_, S. American Pliocene, 146 _Macrotherium_, Miocene of Greece, 116 European Miocene, 121 Madagascar, extinct birds of, 164 description of, 272 mammalia of, 272 birds of, 274 reptiles of, 279 amphibia of, 280 extinct fauna of, 282 general remarks on insect fauna of, 284 Madeira, birds of, 208 land shells of, 208 beetles of, 210 wingless insects numerous in, 211 how stocked with animals, 213 Malacca, Sumatra, and Borneo, zoological unity of, 353 comparison of mammalia, 354 of birds, 355 Malagasy sub-region, description of, 272 mammalia of, 272 birds of, 274 illustration of zoology of, 278 reptiles of, 279 amphibia of, 280 extinct fauna of, 282, 289 insects of, 282 early history of, 286 Malaya and Indo-Malaya, terms defined, 345 (_note_) Malayan forms of life reappearing in West Africa, 263 fauna, probable origin of, 359 resemblances to that of Madagascar and Ceylon explained, 361 Malta, Post-Pliocene fauna of, 114 formerly joined to Africa, 201 fossil elephants of, 201 birds of, 206 (_note_) Mammalia, means of dispersal of, 10 as limited by climate, 11 as limited by rivers, 12 how far limited by the sea, 13 dispersed by ice-floes and drift-wood, 14 means of dispersal of aquatic, 15 of most importance in determining zoological regions, 57 classification of, 85 birthplace and migrations of some families of, 142, 153 cosmopolitan groups of, 176 of the Palæarctic region, 181 of the European sub-region, 192 of the Mediterranean sub-region, 202 of the Siberian sub-region, 217 characteristic of Western Tartary, 218 of the Manchurian sub-region, 222 Palæarctic genera of, in the Manchurian sub-region, 222 Oriental genera of, on borders of same sub-region, 223 peculiar to Japan, 223 characteristic of N. W. China and Mongolia, 226 table of Palæarctic families of, 234 range of Palæarctic genera of, 239 of the Ethiopian region, 253 absence of certain important groups, 253 of the East African sub-region, 260 of West Africa, 262 of S. Africa, 267 of Madagascar, 272 table of Ethiopian families of, 294 table of Ethiopian genera of, 300 of the Oriental region, 315 range of the genera inhabiting the Indian sub-region, 322 of Ceylon, 327 of the Indo-Chinese sub-region, 330 of the Indo-Malayan sub-region, 336 illustration of characteristic Malayan, 336 of the Philippine Islands, 345 table of Oriental families of, 365 table of Oriental genera of, 371 of Australian region, 390 of the Papuan Islands, 410 of the Moluccas, 417 of Timor group, 422 of Celebes, 427 of Australia, 439 illustration of, 439 of New Zealand, 450 table of families of Australian, 470 table of genera of Australian, 475 _Mammal_, the most ancient American, 134 _Mammalia_, extinct, of Old World, 107 extinct, of historic period, 110 extinct, comparative age of in Europe, 127 extinct, of the New World, 129 {498} extinct, of N. America and Europe, compared, 141 original birth-place of some families and genera, 142, 153 of the secondary period, 160 _Manatus_, N. American Post-Pliocene, 130 Manchurian sub-region, description of, 220 mammalia of, 222 birds of, 223 reptiles and amphibia of, 227 fresh-water fish of, 227 insects of, 227 coleoptera of, 228 Marquesas Islands, birds of, 443 Marsh, Mr., on improvability of Asiatic and African deserts, 200 on camels and goats as destructive to vegetation, 200 Marsupials, classification of, 91 N. American Post-Pliocene, 130 European Miocene, 121 first migration to America, 155 diversified forms of, 391 of America prove no connexion with Australia, 399 list of Australian genera of, 476 _Martes_, N. American Tertiary, 135 Mascarene Islands, zoology of, 280 extinct fauna of, 282 gigantic land-tortoises of, 289 _Mastodon_, European Pliocene, 113 Miocene of Greece, 116 European Miocene, 120 in Brazilian caves, 144 S. American Pliocene, 147 Indian Miocene, 123 N. American Post-Pliocene, 130 N. American Tertiary, 138 Mauritius, zoology of, 280 reptiles of, 281 McCoy, Professor, on Palæontology of Victoria, 466 Mediterranean, recent changes in, 39 sub-region, description of, 199 mammalia of, 202 birds of, 203 reptiles and amphibia of, 204 fresh-water fish of, 205 insects of, 205 islands of, 206 sea not separating distinct faunas, 201 _Megacerops_, N. American Tertiary, 137 _Megalomeryx_, N. American Tertiary, 138 _Megalocnus_, fossil in Cuba, 148 _Megalonyx_, N. American Post-Pliocene, 130 in Brazilian caves, 145 S. American Pliocene, 147 _Megalostoma_, Eocene, 169 _Megamys_, S. American Eocene, 148 _Megaspira_, European Tertiary, 169 _Megatheridæ_, in Brazilian caves, 145 _Megatherium_, N. American Post-Pliocene, 130 in Brazilian caves, 145 S. American Pliocene, 147 _Melania_, European secondary, 169 _Meleagris_, N. American Miocene, 163 _Mellivora_, Indian Miocene, 121 _Melolonthidium_, Oolitic insect, 167 _Meniscotherium_, N. American Tertiary, 138 _Menotherium_, N. American Tertiary, 133 _Mephitis_, in Brazilian caves, 144 _Merychus_, N. American Tertiary, 138 _Merychippus_, N. American Tertiary, 135 _Merychochoerus_, N. American Tertiary, 138 _Merycodus_, N. American Tertiary, 138 _Merycopotamus_, Indian Miocene, 122 _Merycotherium_ of Siberian drift, 112 _Mesacodon_, N. American Tertiary, 133 _Mesohippus_, N. American Tertiary, 135 _Mesonyx_, N. American Tertiary, 134 _Mesopithecus_, Miocene of Greece, 115 Meyer, Dr. A. B., on reptiles and amphibia of New Guinea, 415 _Microlestes_, oldest European mammal, 160 _Micromeryx_, European Miocene, 120 _Microsyops_, N. American Tertiary, 133 _Microtherium_, European Miocene, 120 Middendorf, on extreme northern birds, 219 Migrating birds, in which region to be placed, 185 Migration of animals, 10 general phenomena of, 18 of birds, 19 of birds in Europe, 19 probable origin of, 22 of birds in India and China, 23 of birds in N. America, 23 changes in extent of, 24 of birds in S. Temperate America, 25 general remarks on, 25 _Milvus_, European Miocene, 162 Miocene fauna of the Old World, 114 fauna of Greece, 115 fauna of Greece, summary of, 116 fauna of Central Europe, 117 deposits of Siwalik Hills, 121 faunas of Europe and Asia, general observations on, 123 _Miohippus_, N. American Tertiary, 135 Mivart, Professor, on classification of primates, 86 on classification of insectivora, 87 on classification of amphibia, 101 Moles almost wholly Palæarctic, 181 Mole-rat, of W. Tartary, 218 Mollusca, means of dispersal of, 30 classification of, 104 groups selected for study, 104 Moluccas, zoology of, 417 birds of, 419 reptiles of, 420 insects of, 420 peculiarities of fauna of, 421 Monkeys on the high Himalayas, 12 fossil in N. American Miocene in E. Thibet, 222 abundance of in the Oriental region, 315 Monotremata, classification of, 91 list of Australian genera of, 477 "More-pork" of Australia, figure of, 442 _Morotherium_, N. American Pliocene, 140 _Motacilla_, European Miocene, 161 Mound-builders, peculiar Australian birds, 393 Moupin, position and zoology of, 221 _Muridæ_, S. American Pliocene, 147 Murray, Mr. Andrew, on zoological region, 60 _Mustela_, Miocene of Greece, 115 European Miocene, 118 S. American Pliocene, 146 _Mustelidæ_, in Brazilian caves, 144 _Mylodon_, N. American Post-Pliocene, 130 S. American Pliocene, 147 _Myogale_, European Miocene, 118 _Myomorphus_, fossil in Cuba _Myopotamus_, in Brazilian caves, 145 _Myoxus_, European Miocene, 120 European Eocene, 126 _Mysarachne_, European Miocene, 118 _Mysops_, N. American Eocene, 140 _Myxophagus_, N. American Post-Pliocene, 130 N. {499} _Nanohyus_, N. American Tertiary, 137 _Nasua_, in Brazilian caves, 144 Nearctic region, defined, 79 subdivisions of, 80 distinct from Palæarctic, 79 _Necrornis_, European Miocene, 161 Neotropical region, defined, 78 subdivisions of, 78 relations of W. African sub-region with, 265 _Nesodon_, S. American Pliocene, 147 Newton, Professor, on position of _Menuridæ_ and _Atrichiidæ_, 95 on birds of Iceland, 198 New Caledonia, birds of, 444 New Guinea, zoology of, 409 mammalia of, 410 birds of, 411 peculiarities of its ornithology, 413 illustration of ornithology of, 414 reptiles and amphibia of, 415 insects of, 416 New Zealand, objections to making a primary zoological region, 62 extinct birds of, 164 sub-region, description of, 449 compared with British Isles, 449 mammalia of, 451 islets of, 453 illustration of ornithology of, 455 reptiles of, 456 amphibia of, 457 fresh-water fish of, 457 insects of, 458 Longicorns of, 458 Myriapoda of, 458 land-shells of, 459 ancient fauna of, 460 origin of fauna of, 460 poverty of insects in, 462 relations of insect-fauna and flora, 472 Nicobar Islands, their zoological relations, 332 Nightingale, migration of the, 21 Norfolk Island, birds of, 453 North America, remarks on Post-Pliocene fauna of, 130 Post-Pliocene fauna of, partly derived from S. America, 131 extinct birds of, 163 North Africa, zoological relations of, 202 _Notharctos_, N. American Tertiary, 133 Notornis of New Zealand, 455 _Nototherium_, Australian Post-Tertiary, 157 O. _Ochotherium_, in Brazilian caves, 145 _Octodontidæ_, S. American Pliocene, 147 Ophidia, classification of, 99 _Opisthocomus_, Brazilian caves, 164 _Opossum_, extinct, in European Miocene, 121 _Oreodon_, N. American Tertiary, 138 _Oreodontidæ_, N. American Tertiary, 138 Oriental region, defined, 75 subdivisions of, 75 description of, 314 zoological features of, 315 mammalia of, 315 birds of, 316 reptiles of, 317 amphibia of, 317 fresh-water fishes of, 318 summary of vertebrata, 318 insects of, 318 sub-regions of, 321 concluding remarks on, 362 tables of distribution of animals of, 364 Oriental relations of W. African sub-region, 265 Oriental and Palæarctic faunas once identical, 362 Oriental and Ethiopian faunas, cause of their resemblances, 363 _Orohippus_, N. American Tertiary, 136 _Ostrich_, Miocene of N. India, 162 _Otaria_, European Miocene, 118 _Ovibos_, N. American Post-Pliocene, 130 Oxen, birthplace and migrations of, 155 Palæarctic, 182 _Oxyæna_, N. American Tertiary, 134 _Oxygomphus_, European Miocene, 118 _Oxymycterus_, in Brazilian caves, 145 S. American Pliocene, 147 P. _Pachyæna_, N. American Tertiary, 134 _Pachynolophus_, European Eocene, 126 _Pachytherium_, in Brazilian caves, 145 Palæarctic region, defined, 71 subdivisions of, 71 general features of, 180 zoological characteristics of, 181 has few peculiar families, 181 mammalia of, 181 birds of, 182 high degree of speciality of, 184 reptiles and amphibia of, 186 fresh-water fish of, 186 summary of vertebrata of, 186 insects of, 186 coleoptera of, 187 number of coleoptera of, 189 land-shells of, 190 sub-regions of, 190 general conclusions on the fauna of, 231 tables of distribution of animals of, 233 _Palæacodon_, N. American Tertiary, 133 _Palæetus_, European Miocene, 162 _Palægithalus_, European Eocene, 162 _Palælodus_, European Miocene, 162 _Palæocastor_, N. American Tertiary, 140 _Palæocercus_, European Miocene, 162 _Palæochoeus_, European Miocene, 119 _Palæohierax_, European Miocene, 162 _Palæolagus_, N. American Tertiary, 140 _Palæolama_, S. American Pliocene, 147 _Palæomephitis_, European Miocene, 118 _Palæomeryx_, European Miocene, 120 _Palæomys_, European Miocene, 121 _Palæontina oolitica_, Oolitic insect, 167 Palæontology, 107 how best studied in its bearing on geographical distribution, 168 as an introduction to the study of geographical distribution, concluding remarks on, 169 _Palæonyctis_, European Eocene, 125 _Palæoperdix_, European Miocene, 161 _Palæophrynus_, European Miocene, 166 _Palæoreas_, Miocene of Greece, 116 _Palæortyx_, European Miocene, 161 _Palæoryx_, Miocene of Greece, 116 _Palæospalax_, 111 European Miocene, 117 _Palæosyops_, N. American Tertiary, 136 _Palæotheridæ_, European Eocene, 125 _Palæotherium_, European Eocene, 125 S. American Eocene, 148 _Palæotragus_, Miocene of Greece, 116 _Palæotringa_, N. American Cretaceous, 164 _Palapterygidæ_ of New Zealand, 164 {500} Palestine, birds of, 203 _Paloplotherium_, European Miocene, 119 European Eocene, 125 _Paludina_, Eocene, 169 European Secondary, 169 Pampas, Pliocene deposits of, 146 Panda, of Nepaul and E. Thibet, 222 Himalayan, figure of, 331 _Panolax_, N. American Tertiary, 140 Papuan Islands, zoology of, 409 Paradise-bird, twelve-wired, figure of, 414 _Parahippus_, N. American Tertiary, 136 _Paramys_, N. American Eocene, 140 Parroquet, Papuan, figure of, 415 Parrots, classification of, 96 Passeres, arrangement of, 94 range of Palæarctic genera of, 243 range of Ethiopian genera of, 306 range of Oriental genera of, 375 range of Australian genera of, 478 _Patriofelis_, N. American Tertiary, 134 Peculiar groups, geographically, how defined, 184 _Pelagornis_, European Miocene, 162 _Pelonax_, N. American Tertiary, 138 _Peratherium_, European Miocene, 121 European Eocene, 126 _Perchoerus_, N. American Tertiary, 137 Perim Island, extinct mammalia of, 122 probable southern limit of old Palæarctic land, 362 _Perissodactyla_, N. American Tertiary, 135 Persia, birds of, 204 _Phascolomys_, Australian Post-Tertiary, 157 _Phasianus_, Miocene of Greece, 116 European Post-Pliocene, 161 Pheasants, in European Miocene, 161 golden, of N. China, 226 eared, of Mongolia, 226 _Phenacodus_, N. American Tertiary, 138 Philippine Islands, mammals of, 345 birds of, 346 origin of peculiar fauna of, 348 _Phocidæ_, N. American Tertiary, 140 _Phyllomys_, in Brazilian caves, 145 _Phyllostomidæ_, in Brazilian caves, 144 Physical changes affecting distribution, 7 _Physeter_, European Pliocene, 112 Picariæ, arrangement of, 95 range of Palæarctic genera of, 247 range of Ethiopian genera of, 309 range of Oriental genera of, 381 range of Australian genera of, 482 _Picus_, European Miocene, 161 Pigeons, classification of, 96 remarkable development of, in the Australian region, 395 crested, of Australia, figure of, 441 Pigs, power of swimming, 13 Pikermi, Miocene fauna of, 115 Pittidæ, abundant in Borneo, 355 _Plagiolophus_, European Eocene, 126 _Planorbis_, European Secondary, 169 Eocene, 169 _Platycercidæ_, gorgeously-coloured Australian parrots, 394 _Platygonus_, N. American Post-Pliocene, 130 _Plesiarctomys_, European Eocene, 126 _Plesiomeryx_, European Eocene, 126 _Plesiosorex_, European Miocene, 118 Pliocene period, Old World, mammalia of, 112 Pliocene and Post-Pliocene faunas, of Europe, general conclusions from, 113 of N. America, 132 of S. America, 146 of Australia, 157 _Pliohippus_, N. American Tertiary, 135 _Pliolophus_, European Eocene, 126 _Pliopithecus_, European Miocene, 117 _Poebrotherium_, N. American Tertiary, 138 Polynesian sub-region, description of, 442 birds of, 443 reptiles of, 447 Post-Pliocene, mammalia of Europe, 110 remains imply changes of physical geography in Europe, 111 fauna of N. America, 129 fauna of N. America, remarks on, 130 Potamogale of West Africa, figure of, 264 _Potamotherium_, European Miocene, 118 Potto of West Africa, figure of, 264 _Praotherium_, N. American Post-Pliocene, 130 Primates, classification of, 86 probable birthplace of, 153 range of Palæarctic genera of, 239 range of Ethiopian genera of, 300 range of Oriental genera of, 371 range of Australian genera of, 475 _Primates_, European Pliocene, 112 Miocene of Greece, 115 European Miocene, 117 Indian Miocene, 121 European Eocene, 124 N. American Tertiary, 132 of Brazilian caves, 144 Prince's Island, birds of, 266 _Prionidium_, Oolitic insects, 167 _Pristiphoca_, in European Pliocene, 112 Proboscidea, classification of, 90 range of Ethiopian genus, 303 range of Oriental genus, 374 _Proboscidea_, European Pliocene, 113 Miocene of Greece, 116 European Miocene, 120 Indian Miocene, 122 N. American Post-Pliocene, 130 N. American Tertiary, 138 of Brazilian caves, 144 S. American Pliocene, 147 _Procamelus_, N. American Post-Pliocene, 130 N. American Tertiary, 138 _Procyon_, N. American Post-Pliocene, 130 _Procyonidæ_, in Brazilian caves, 144 _Promephitis_, Miocene of Greece, 115 European Miocene, 118 Promerops of East Africa, figure of, 261 _Propalæotherium_, European Eocene, 126 _Protemnodon_, Australian Post-Tertiary, 157 _Protohippus_, N. American Tertiary, 135 _Protomeryx_, N. American Tertiary, 138 _Protopithecus_, in Brazilian caves, 144 _Prototomus_, N. American Tertiary, 134 _Protornis_, European Eocene, 162 _Pseudælurus_, European Miocene, 118 _Pseudocyon_, European Miocene, 118 Psittaci, classification of, 96 range of Ethiopian genera of, 311 range of Oriental genera of, 383 range of Australian genera of, 484 _Psittacus_, European Miocene, 161 _Pterocles_, European Miocene, 161 _Pterodon_, European Eocene, 125 _Pupa_, Eocene, 169 _Pupa vetusta_, Palæozoic, 169 _Pythonidæ_, European Miocene, 165 R. Racoon-dog of N. China, 226 _Rana_, European Miocene, 166 Region, the best term for the primary zoological divisions, 68 {501} Arctic, why not adopted, 69 Palæarctic, defined, 71 Palæarctic, subdivisions of, 71 Ethiopian, defined, 73 Ethiopian, subdivisions of, 73 Oriental, defined, 75 Oriental, subdivisions of, 75 Australian, defined, 77 Australian, subdivisions of, 77 Neotropical, defined, 78 Neotropical, subdivisions of, 78 Nearctic, defined, 79 Nearctic, distinct from Palæarctic, 79 Nearctic, subdivisions of, 80 Regions, zoological, 50 zoological, how they should be formed, 53 zoological, may be defined by negative or positive characters, 54 zoological, by what class of animals best determined, 56 for each class of animals, not advisable, 58 zoological, proposed since 1857, 58 zoological, Mr. Sclater's, 59 zoological, discussion of those proposed by various authors, 61 zoological, proportionate richness of, 64 temperate and tropical, well marked in northern hemisphere, 65 and zones, table of, 66 comparative richness of, 81 and sub-regions, table of, 81 order of succession of the, 173 Representative species, 4 Reptiles, means of dispersal of, 28 classification of, 98 Miocene of Greece, 116 of Indian Miocene deposits, 123 extinct Tertiary, 165 cosmopolitan groups of, 176 peculiar to Palæarctic region, 186 of Central Europe, 195 of the Mediterranean sub-region, 204 of Siberian sub-region, 220 of the Manchurian sub-region, 227 table of Palæarctic families of, 236 of the Ethiopian region, 254 of the East African sub-region, 260 of West Africa, 264 S. African, 268 of Madagascar, 279 table of Ethiopian families of, 297 of the Oriental region, 317 of the Indian sub-region, 326 of Ceylon, 327 of Indo-Chinese sub-region, 331 of Indo-Malay sub-region, 340 table of Oriental families of, 368 of the Australian region, 396 of New Guinea, 415 of the Moluccas, 420 of the Polynesian sub-region, 447 of New Zealand, 456 table of Australian families of, 472 _Rhea_, in Brazilian caves, 164 _Rhinoceros_, Post-Pliocene, 112 European Pliocene, 113 Miocene of Greece, 116 Indian Miocene, 122 fossil remains of, at 16,000 feet elevation in Thibet, 122 fossil in N. China, 123 N. American Tertiary, 136 Rhinoceros-hornbill, figure of, 339 _Rhinocerotidæ_, N. American Tertiary, 136 River-hog, of West Africa, figure of, 264 of Madagascar, figure of, 278 Rivers, limiting the range of mammalia, 12 limiting the range of birds, 17 River-scene, in West Africa, 264 Rodentia, classification of, 90 range of Palæarctic genera of, 242 range of Ethiopian genera of, 304 range of Oriental genera of, 374 range of Australian genera of, 476 _Rodentia_, European Pliocene, 113 Miocene of Greece, 116 European Miocene, 120 European Eocene, 126 N. American Post-Pliocene, 130 N. American Tertiary, 139 of Brazilian caves, 144 S. American Pliocene, 147 of S. American Eocene, 148 Ruff, figure of, 195 S. Sahara, a debatable land, 251 Saiga, antelope of W. Tartary, 218 Samoa Islands, birds of, 443 Sandwich Islands, birds of, 445 probable past history of, 446 mountain plants of, 446 depth of ocean around, 447 Sand grouse, Pallas, of Mongolia, 226 _Satyrites Reynesii_, European Cretaceous insect, 167 Saunders, Mr. Edward, on the Buprestidæ of Japan, 229 _Scelidotherium_, in Brazilian caves, 145 S. American Pliocene, 147 _Schistopleurum_, S. American Pliocene, 147 Schweinfurth, Dr., on natural history of Central Africa, 252 on limits of W. African sub-region, 262 (_note_) _Sciurus_, European Miocene, 120 European Eocene, 126 _Sciuravus_, N. American Eocene, 140 Sclater, Mr., on zoological regions, 59 why his six regions are adopted, 63 on birds of Sandwich Islands, 445 Sea, as a barrier to mammalia, 13 Seals, fossil in European Miocene, 118 of Lake Baikal, 218 Secondary formations, mammalian remains in, 159 Secretary-bird of Africa, figure of, 261 _Semnopithecus_, European Pliocene, 112 Miocene of Greece, 115 European Miocene, 117 Indian Miocene, 121 Semper, Dr., on Philippine mammalia, 345 _Serpentarius_, European Miocene, 162 Seychelle Islands, zoology of, 281 amphibia of, 281 Sharp, Dr., on Japan beetles, 229 Sharpe, Mr. R. B., his arrangement of Accipitres, 97 on birds of Cape Verd Islands, 215 Sheep, Palæarctic, 182 Siberia, climate of, 217 Siberian sub-region, description of, 216 mammalia of, 217 birds of, 219 reptiles and amphibia of, 220 insects of, 220 _Simocyon_, Miocene of Greece, 115 _Sinopa_, N. American Tertiary, 134 {502} Sirenia, classification of, 89 range of Ethiopian genera of, 303 range of Oriental genus, 374 range of Australian genus of, 476 _Sirenia_, European Pliocene, 112 European Miocene, 119 _Sivatherium_, Indian Miocene, 122 Siwalik Hills, Miocene deposits of, 121 Smith, Mr. Frederick, on Hymenoptera of Japan, 230 Snake, at great elevation in Himalayas, 220 Snakes, classification of, 99 Eocene, 165 large proportion of venomous species in Australia, 396 of New Zealand, 457 Society Islands, birds of, 443 _Soricictis_, European Miocene, 118 _Soricidæ_, European Miocene, 118 South African sub-region, description of, 266 mammalia of, 267 birds of, 267 reptiles of, 268 amphibia of, 268 fresh-water fish of, 268 butterflies of, 268 coleoptera of, 268 summary of its zoology, 269 South America, fossil fauna of, 143 Pliocene deposits of, 146 supposed land connection with Australia, 398 South Australia, peculiar birds of, 441 Species, representative, 4 _Speothos_, in Brazilian caves, 144 _Spermophilus_, European Miocene, 120 _Sphenodon_, in Brazilian caves, 145 _Sphinx_, in European Oolite, 167 St. Helena, zoological features of, 269 coleoptera of, 270 landshells of, 271 St. Thomas' Island, birds of, 266 Stations, definition of, 4 _Steneofiber_, European Miocene, 120 _Sthenurus_, Australian Post-Tertiary, 157 _Strix_, European Miocene, 162 Struthiones, arrangement of, 98 range of Ethiopian genera of, 313 range of Australian genera of, 485 Struthious birds, probable origin of, 287 _Stylinodontidæ_, N. American Eocene, 139 _Stylinodontia_, N. American Eocene, 139 Sub-regions, on what principle formed, 80 Palæarctic, 191 Ethiopian, 258 Oriental, 321 Australian, 408 _Suidæ_, European Miocene, 119 Sula Islands, fauna of, 433 _Sus_, European Pliocene, 113 Miocene of Greece, 116 European Miocene, 119 Indian Miocene, 122 Swinhoe, Mr., on zoology of Formosa and Hainan, 332 _Symborodon_, N. American Tertiary, 137 _Synaphodus_, European Miocene, 119 _Synoplotherium_, N. American Tertiary, 134 T. Tables of distribution of families and genera explained, 177 _Talpa_, European Miocene, 117 _Tapir_, fossil in N. China, 123 Tapirs, birthplace and migrations of, 154 Tapir, Malayan, figure of, 337 _Tapiridæ_, European Eocene, 125 _Tapirus_, European Pliocene, 113 Indian Miocene, 122 in Brazilian caves, 144 Tarsier, Malayan, figure of, 337 Tasmania, comparative zoological poverty of, 441 _Taxodon_, European Miocene, 118 _Telmatobius_, N. American Cretaceous, 164 _Telmatolestes_, N. American Tertiary, 133 _Testudo_, Miocene of Greece, 116 Indian Miocene, 123 Testudo, great antiquity of the genus, 289 _Tetrachus_, European Miocene, 117 _Tetrao albus_, in Italian caverns, 161 _Thalassictis_, Miocene of Greece, 115 European Miocene, 118 _Theridomys_, European Miocene, 126 European Eocene, 126 S. American Eocene, 148 _Thinohyus_, N. American Tertiary, 137 _Thinolestes_, N. American Tertiary, 133 _Thylacinus_, Australian Post-Tertiary, 157 _Thylacoleo_, Australian Post-Tertiary, 157 _Tillodontia_, N. American Eocene, 139 _Tillotheridæ_, N. American Eocene, 139 _Tillotherium_, N. American Eocene, 139 Timor, physical features of, 389 group, mammalia of, 422 birds of, 422 origin of fauna of, 424 insects of, 426 _Tinoceras_, N. American Eocene, 139 _Titanomys_, European Miocene, 121 _Titanotherium_, N. American Tertiary, 137 _Tomarctos_, N. American Tertiary, 135 Tonga Islands, birds of, 443 Tortoises, classification of, 100 of Mascarene Islands and Galapagos, 289 Touraco of W. Africa, figure of, 264 _Toxodon_, S. American Pliocene, 137 _Toxodontidæ_, S. American Pliocene, 147 _Trachytherium_, European Miocene, 119 _Tragocerus_, Miocene of Greece, 116 European Miocene, 120 Tragopan, Himalayan, figure of, 331 Tree-shrew of Borneo, figure of, 337 Tree-kangaroo, figure of, 415 _Trichechus_, N. American Post-Pliocene, 130 Trichoglossidæ, birds specially adapted to Australia, 393 _Trionyx_, Indian Miocene, 123 Miocene and Eocene, 165 Tristan d'Acunha, zoology of, 271 Tristram, Canon, summary of the birds of Palestine, 203 Trogon, European Miocene, 161 _Trogontherium_, Post-Pliocene of Europe, 111 _Trucijelis_, N. American Post-Pliocene, 129 Tundras of Siberia, greatest extent of, 216 _Tupaiidæ_, European Miocene, 118 Turner, Mr., on classification of Edentata, 90 _Tylodon_, European Eocene, 125 _Typotherium_, S. American Pliocene, 147 U. _Uintacyon_, N. American Tertiary, 134 _Uintatherium_, N. American Eocene, 139 _Uintornis_, N. American Eocene, 163 _Unio_, European Secondary, 169 Ungulata, classification of, 89 antiquity of, 151 {503} of the Palæarctic region, 182 range of Palæarctic genera of, 241 range of Ethiopian genera of, 303 range of Oriental genera of, 374 range of Australian genera of, 476 _Ungulata_, European Pliocene, 112 Miocene of Greece, 115 European Miocene, 119 Indian Miocene, 121 European Eocene, 125 N. American Post-Pliocene, 130 N. American Tertiary, 135 of Brazilian caves, 144 S. American Pliocene, 146 Urania of Madagascar, 282 _Ursidæ_, N. American Tertiary, 135 in Brazilian caves, 144 _Ursitaxus_, Indian Miocene, 121 _Ursus_, Post-Pliocene, 112 Indian Miocene, 121 V. Vanga of Madagascar, figure of, 278 _Varanus_, Miocene of Greece, 116 Indian Miocene, 123 Vertebrata, summary of Palæarctic, 186 summary of Ethiopian, 255 summary of Oriental, 318 summary of Australian, 397 _Vespertilio_, European Eocene, 125 _Viperus_, European Miocene, 165 _Viverra_, European Pliocene, 112 European Miocene, 118 _Viverridæ_, European Miocene, 118 European Eocene, 125 W. Walden, Viscount, on birds of Philippine Islands, 346 on birds of Celebes, 428 _Washakius_, N. American Tertiary, 134 Waterhouse, Mr. G. R., on classification of rodentia, 90 on classification of marsupials, 91 West African sub-region, description of, 262 mammalia of, 262 birds of, 262 Oriental or Malayan element in, 263 river scene with characteristic animals, 264 reptiles of, 264 amphibia of, 264 Oriental and Neotropical relations of, 265 insects of, 265 land-shells of, 265 islands of, 265 West Australia, peculiar birds of, 441 Whydah finch of W. Africa, figure of, 264 Wollaston, Mr. T. V., on the coleoptera of the Atlantic Islands, 209 on the wings of the Madeiran beetles, 211 on the origin of the insect fauna of the Atlantic Islands, 214 on coleoptera of the Cape Verd Islands, 215 on beetles of St. Helena, 270 X. _Xenurus_, in Brazilian caves, 145 _Xiphodontidæ_, European Miocene, 119 Z. _Zeuglodontidæ_, N. American Tertiary, 140 _Zonites priscus_, Palæozoic, 169 Zoological characteristics of Palæarctic region, 181 Ethiopian region, 252 Oriental region, 315 Australian region, 390 Zoological regions, discussion on, 50 END OF VOL. I. LONDON: R. CLAY, SONS, AND TAYLOR, PRINTERS, BREAD STREET HILL. Notes [1] Marcel de Serres states this as a general fact for wading and swimming birds. He says that the old birds arrive in the extreme north almost alone, the young remaining on the shores of the Baltic, or on the lakes of Austria, Hungary, and Russia. See his prize essay, _Des Causes des Migrations_, &c. 2nd. ed., Paris, 1845, p. 121. [2] Quoted in Lyell's _Principles of Geology_ (11th ed. vol. ii. p. 374), from _Amoen. Acad. Essay 75_. [3] This estimate has been made for me by Mr. Stanford from the materials used in delineating the contours of the ocean-bed on our general map. It embodies the result of all the soundings of the _Challenger_, _Tuscarora_, and other vessels, obtainable up to August, 1875. [4] Mr. John Hickman of Desborough. [5] _Trans. Zool. Soc. of London_, vol. viii. p. 381. [6] Malta is interesting as forming a resting-place for migratory birds, while crossing the Mediterranean. It has only eight land and three aquatic birds which are permanent residents; yet no less than 278 species have been recorded by Mr. E. A. Wright as visiting or passing over it, comprising a large proportion of the European migratory birds. The following are the permanent residents: _Cerchneis tinnunculus_, _Strix flammea_, _Passer salicicola_, _Emberiza miliaria_, _Corvus monedula_, _Monticola cyanea_, _Sylvia conspicillata_, _Columba livia_, _Puffinus cinereus_, _P. anglorum_, _Thalassidroma pelagica_. [7] A remarkable confirmation of this theory, is furnished in the Report to the Royal Society of the naturalist to the Kerguelen Island, "Transit Expedition"--the Rev. A. E. Eaton. Insects were assiduously collected, and it was found that almost all were either completely apterous, or had greatly abbreviated wings. The only moth found, several flies, and numerous beetles, were alike incapable of flight. As this island is subject to violent, and almost perpetual gales, even in the finest season, the meaning of the extraordinary loss of wings in almost all the insects, can, in this case, hardly be misunderstood. [8] The facts on which these statements rest, will be found more fully detailed in the Author's Presidential Address to the Entomological Society of London for the year 1871. [9] _Quarterly Journal of the Geological Society_, 1874, p. 494. [10] Dr. Schweinfurth has accurately determined the limits of the sub-region at the point where he crossed the watershed between the Nile tributaries and those of the Shari, in 4½° N. Lat. and 28½° E. Long. He describes a sudden change in the character of the vegetation, which to the southward of this point assumes a West-African character. Here also the chimpanzee and grey parrot first appear, and certain species of plants only known elsewhere in Western Africa. [11] There are also some special resemblances between the plants of Madagascar and South Africa, according to Dr. Kirk. [12] As so many typical Malay groups are absent only from the Philippines, I have adopted the term "Malaya," to show the distribution of these, using the term "Indo-Malaya" when the range of the group includes the Philippines. This must be remembered when consulting the tables of distribution at the end of this chapter. [13] See _Ann. Nat. Hist._, 1873, p. 418, where the species is said to inhabit the Aru Islands and Celebes, which renders it not improbable that it may have been carried to the former islands from the latter. [14] I also find about this proportion in my Amazonian collections, even counting all the humming-birds, parrots, and toucans as handsome birds. [15] The general form of the skull agrees best with that of _Cynocephalus mormon_, the largest and most typical of the African baboons; while the position of the nostrils brings it nearer the macaques. [16] A new genus of Beetles (_Apterocyclus_) of the family Lucanidæ, has recently been described from the Sandwich Islands, and it is said to be most nearly related to a group inhabiting Chili,--an indication either of the great antiquity of the fauna, or of the varied accidental migrations from which it has had its origin. *** END OF THE PROJECT GUTENBERG EBOOK THE GEOGRAPHICAL DISTRIBUTION OF ANIMALS, VOLUME 1 *** Updated editions will replace the previous one—the old editions will be renamed. Creating the works from print editions not protected by U.S. copyright law means that no one owns a United States copyright in these works, so the Foundation (and you!) can copy and distribute it in the United States without permission and without paying copyright royalties. Special rules, set forth in the General Terms of Use part of this license, apply to copying and distributing Project Gutenberg™ electronic works to protect the PROJECT GUTENBERG™ concept and trademark. 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