The Project Gutenberg eBook of Comments on the Taxonomy and Geographic Distribution of North American Microtines This ebook is for the use of anyone anywhere in the United States and most other parts of the world at no cost and with almost no restrictions whatsoever. You may copy it, give it away or re-use it under the terms of the Project Gutenberg License included with this ebook or online at www.gutenberg.org. If you are not located in the United States, you will have to check the laws of the country where you are located before using this eBook. Title: Comments on the Taxonomy and Geographic Distribution of North American Microtines Author: E. Raymond Hall E. Lendell Cockrum Release date: June 22, 2009 [eBook #29201] Most recently updated: January 5, 2021 Language: English Credits: Produced by Chris Curnow, Joseph Cooper and the Online Distributed Proofreading Team at https://www.pgdp.net *** START OF THE PROJECT GUTENBERG EBOOK COMMENTS ON THE TAXONOMY AND GEOGRAPHIC DISTRIBUTION OF NORTH AMERICAN MICROTINES *** Produced by Chris Curnow, Joseph Cooper and the Online Distributed Proofreading Team at https://www.pgdp.net Comments on the Taxonomy and Geographic Distribution of North American Microtines BY E. RAYMOND HALL AND E. LENDELL COCKRUM University of Kansas Publications Museum of Natural History Volume 5, No. 23, pp. 293-312 November 17, 1952 University of Kansas LAWRENCE 1952 UNIVERSITY OF KANSAS PUBLICATIONS, MUSEUM OF NATURAL HISTORY Editors: E. Raymond Hall, Chairman, A. Byron Leonard, Edward H. Taylor, Robert W. Wilson Volume 5, No. 23, pp. 293-312 November 17, 1952 UNIVERSITY OF KANSAS Lawrence, Kansas PRINTED BY FERD VOILAND, JR., STATE PRINTER TOPEKA, KANSAS 1952 Transcriber's Note: The symbol "^" in some numbers in Table I is used to indicate that the number following it are printed in superscript. Comments on the Taxonomy and Geographic Distribution of North American Microtines BY E. RAYMOND HALL and E. LENDELL COCKRUM In preparing maps showing the geographic distribution of North American microtines, conflicting statements in the literature and identifications that, if accepted, would result in improbable geographic ranges have led to the examination of pertinent specimens with the results given below. The studies here reported upon were aided by a contract between the Office of Naval Research, Department of the Navy, and the University of Kansas (Nr 161-791), by funds provided by the University of Kansas from its Research Appropriation, and by grants for out-of-state field work from the Kansas University Endowment Association. Grateful acknowledgment is made to persons in charge of the collections at each of the following institutions for permission to use the collections under their charge: Biological Surveys Collection, United States National Museum (herein abbreviated USBS); California Museum of Vertebrate Zoology (MVZ); Chicago Natural History Museum (CNHM); University of Kansas Museum of Natural History (KU); Museum of Comparative Zoology (MCZ); United States National Museum (USNM); Department of Economic Zoology, University of Wisconsin (UWDEZ); and Zoological Museum, University of Wisconsin (UWZM). Synaptomys cooperi saturatus Bole and Moulthrop 1942. _Synaptomys cooperi saturatus_ Bole and Moulthrop, Sci. Publs. Cleveland Mus. Nat. Hist., 5:149, September 11, type from Bloomington, McLean County, Illinois. When Bole and Moulthrop named _Synaptomys cooperi saturatus_, with type locality in Illinois, they, in effect, divided the geographic range of _Synaptomys cooperi stonei_ into two parts (see A. B. Howell, N. Amer. Fauna, 50:10 (fig. 2), August 5, 1927) since Bole and Moulthrop (_op. cit._) did not assign to any subspecies the specimens from southern Wisconsin that Howell (_op. cit._) had identified as _S. c. stonei_. Bole and Moulthrop's inclusion in their newly named subspecies of a specimen from as far west as East Columbia, Missouri, left in doubt the subspecific identity of specimens from Iowa and a specimen from Arkansas. Howell (_op. cit._) had assigned this material from Iowa and Arkansas to _S. c. gossii_. Howell recognized that the one individual (168266 USBS) from Lake City, Arkansas, was too young to be identified to subspecies with certainty and assigned the specimen to _S. c. gossii_ "upon geographical grounds" (_op. cit._:19). Keith R. Kelson and one of us (Hall) compared this specimen with pertinent materials. As a result of this comparison we refer the specimen, on the same grounds employed by Howell, to _Synaptomys cooperi saturatus_. Specimens from approximately the southern half of Wisconsin (from Kelly Lake southward) were referred to _S. c. stonei_ by Howell (_op. cit._:16). Now that _S. c. saturatus_ has been recognized, these specimens from southern Wisconsin would be expected to be referable to _S. c. saturatus_. When these specimens were examined and compared (by Hall and Kelson) with other specimens in the United States National Museum the skulls were found to be much larger than in _S. c. cooperi_, smaller than in _S. c. gossii_, and nearly the size of those of _Synaptomys cooperi saturatus_, to which subspecies we refer the specimens in question. Howell (_op. cit._:16) referred a specimen from Cassopolis, Michigan, a locality that might be presumed to fall within the range of the more recently named _S. c. saturatus_, to _S. c. stonei_. Bole and Moulthrop did not mention this specimen when they described and named _S. c. saturatus_ (1942). Neither did Burt, but Cassopolis is within the geographic range ascribed to _S. c. cooperi_ on his map (The Mammals of Michigan, Univ. Michigan Press, p. 213, 1946). Examination (by Kelson and Hall) of the specimen (41777 MCZ) reveals that it resembles _S. c. cooperi_ in shortness of hind foot (18 mm.), shortness of tail (18 mm.), narrowness across zygomata (16 mm.), and grayish pelage. In the long braincase, heavy rostrum, greater condylobasilar length, greater lambdoidal breadth, long rostrum, and longer incisive foramina, it agrees closely with specimens of _S. c. saturatus_, to which subspecies we refer the specimen. Necker and Hatfield (Bull. Chicago Acad. Sci., 6:54, 1941) referred specimens from Rosiclaire, Illinois, to _S. c. gossii_. These specimens were not mentioned by Bole and Moulthrop (_op. cit._) when they named _S. c. saturatus_ although the specimens presumably would be referred to the newly-named subspecies. We have examined the pertinent specimens (Nos. 15781-15786 and 16049-16054 CNHM) and find that on the basis of dark color, long and slender skull, heavy incisors, and small cheek-teeth, they are referable to _S. c. saturatus_ Bole and Moulthrop. None, however, has a tail so short as the type of _S. c. saturatus_. For that matter, the average length of the tail of six near topotypes (5 mi. W, 2-1/2 mi. S Monticello, Piatt County, Illinois, Nos. 32037-32042 KU) exceeds that of the type (17.4 mm., range 12-20, as compared to 14 mm. for the type). Synaptomys cooperi gossii (Coues) 1877. _Arvicola (Synaptomys) gossii_ Coues, Monogr. N. Amer. Rodentia, p. 235 (published as a synonym of _Synaptomys cooperi_, but name stated to apply to Kansan specimens of which description and measurements are on p. 236), type from Neosho Falls, Woodson County, Kansas. 1897. _Synaptomys cooperi gossii_, Rhoads, Proc. Acad. Nat. Sci. Philadelphia, 49:307, June. In view of the taxonomic treatment accorded by Bole and Moulthrop (Sci. Publs. Cleveland Mus. Nat. Hist, 5:149-151, September 11, 1942) to the lemming mice of the species _Synaptomys cooperi_, as explained in the preceding account, it has seemed desirable to examine Iowan specimens of this species. Hall and Kelson examined the necessary material and made the following conclusions. An adult male from Hillsboro (168453 USBS) has the lighter color and large skull of _S. c. gossii_ to which Howell (N. Amer. Fauna, 50:19, August 5, 1927) referred the specimen. The more western specimen from Knoxville, a young male (190358 USNM), is almost exactly the same age as a male of _S. c. saturatus_ from Bascom, Indiana (143701 USNM), and is but slightly older than a male _S. c. gossii_ from Ft. Leavenworth, Kansas (91583 USBS). The upper molariform tooth-row is the same length in the specimens from Kansas and Iowa, but is longer in that from Indiana. The fact that the specimen from Knoxville closely resembles the Kansan specimen in other dimensions of the skull, which is larger than in the specimen from Indiana, gives a basis for applying the name _Synaptomys cooperi gossii_ to the specimen from Knoxville. This is the same name recently used by Fichter and Hansen (Bull. Univ. Nebraska State Mus., 3(2):2, September, 1947) for the Iowan specimens, although they seemingly applied the name without being aware of Bole and Moulthrop's earlier naming of _S. c. saturatus_ (Sci. Publs. Cleveland Mus. Nat. Hist., 5:149, September 11, 1942). Synaptomys borealis sphagnicola Preble 1899. _Synaptomys (Mictomys) sphagnicola_ Preble, Proc. Biol. Soc. Washington, 13:43, May 29, type from Fabyans, Coos County, New Hampshire. 1927. _Synaptomys borealis sphagnicola_, A. B. Howell, N. Amer. Fauna, 50:30, August 5. Howell (N. Amer. Fauna, 50:30-31, August 5, 1927) had only eight specimens of this subspecies available when he revised the genus _Synaptomys_. Of these eight (Maine: Mount Katahdin, 2; New Brunswick: Near Bathurst, 1; New Hampshire: Fabyans, 1, the type; Quebec: St. Rose, 4), only the type and one of the specimens from St. Rose are adults. Concerning the others, Howell wrote (_op. cit._:31): "The example from near Bathurst is not adult and has a damaged skull, so is identified provisionally. All other specimens are too young for positive diagnosis." Since Howell's revision only one additional specimen has been reported. Anderson (Ann. Rept. Provancher Soc. for 1939, p. 71, 1940) reported it from Table Mountain, 3888 ft., Gaspé County, Quebec. In the collection of the University of Kansas Museum of Natural History there is still another specimen. It is an adult male topotype (No. 6483 KU, formerly No. 72 in the collection of Alfred E. Preble) obtained on August 21, 1905, at Fabyans, New Hampshire. The measurements of this specimen are as follows (measurements in parenthesis are those of the type as given by Howell, _op. cit._): Total length, 135 (132); tail, 26 (24); hind foot, 22 (20); condylobasilar length, 25.1 (25.8); rostral length, 6.5 (6.8); rostral breadth, 4.7 (4.9); interorbital breadth, 3.3 (2.8); zygomatic breadth, 15.4 (16.0); lambdoidal breadth, 12.1 (12.4); incisive foramina, 5.9 (5.7); height of skull, 9.1 (9.3). Howell (_op. cit._:30) characterized _S. b. sphagnicola_ as: "Large and high [skull] with narrow interorbital sharply ridged, the ridges of the type being joined for a distance of 4 millimeters; interparietal narrow and rectangular. The rostrum is long, tapering very little, and the nasals, slightly constricted medially are quite narrow posteriorly. The incisive foramina are long and wide." Howell further stated (_op. cit._:30-31) that: "It is hard to predict what will be found to constitute the most valuable cranial characters in distinguishing this race from adult _medioximus_. The discernible differences now are in the shape of the interparietals, rostral characters, and interorbital differences that will probably not hold good when animals of the same age are compared." As can be seen from a comparison of the measurements given above for the type and the topotype, some of the characteristics given by Howell are not found in the topotype: The interorbital region is not narrow (in fact it is wider than it ordinarily is in some other subspecies of _Synaptomys borealis_) and the incisive foramina are not longer than in other subspecies of _Synaptomys borealis_. As far as present material permits us to judge, _Synaptomys borealis sphagnicola_ is characterized, cranially, by: Skull large; interorbital region sharply ridged (the ridges being joined for a distance of 4 mm. in the type and of 4.5 mm. in the topotype); rostrum long, tapering relatively little; nasals slightly constricted medially and unusually narrow posteriorly; interparietal narrow and rectangular. Clethrionomys occidentalis caurinus (Bailey) 1898. _Evotomys caurinus_ Bailey, Proc. Biol. Soc. Washington, 12:21, January 27, type from Lund, east shore Malaspina Inlet, British Columbia. 1935. _Clethrionomys gapperi caurinus_, Racey and Cowan, Rept. British Columbia Prov. Mus. for 1935, p. H 25. Prior to 1935 _caurinus_ was considered to be a monotypic species. In 1935 Racey and Cowan (Rept. British Columbia Provincial Museum for 1935, pp. H 25-H 26) examined material from southwestern British Columbia of _C. caurinus_, including a series of 24 specimens from Alta Lake, and compared it with _Clethrionomys gapperi occidentalis_ and _C. g. saturatus_. They found _caurinus_ to be distinct from _C. g. saturatus_ but were "not convinced that _occidentalis_ and _caurinus_ both merit systematic recognition; should they prove to be indistinguishable, as the little available material indicates, _occidentalis_ will take precedence on grounds of priority. It is our opinion that further study of the distribution of the genus in British Columbia will lead to the recognition of _occidentalis_ as the form inhabiting coast-line and _saturatus_ the interior of British Columbia" p. H 26. In the face of these opinions Racey and Cowan nevertheless recognized _caurinus_ under the name _Clethrionomys gapperi caurinus_ (Bailey). In spite of the treatment by Racey and Cowan (_op. cit._) of _occidentalis_ and _caurinus_ as subspecies of _C. gapperi_, later authors arranged _occidentalis_ as a member of the "_californicus_" group although they retained _caurinus_ in the _gapperi_ group. For example, Davis (The Recent Mammals of Idaho, The Caxton Printers, pp. 307-308, 1939) assigned _C. caurinus_ to the _gapperi_ group, although he regarded _C. caurinus_ as a species (not a subspecies). He regarded also _C. occidentalis_ as a species (not a subspecies) but assigned it to the _californicus_ group. Dalquest (Univ. Kansas Publ., Mus. Nat. Hist., 2:344, April 9, 1948) considered _occidentalis_ to be conspecific with _Clethrionomys californicus_ and wrote (_op. cit._:101): "The _californicus_ group, I feel, contains only the races of _Clethrionomys californicus_, while the _gapperi_ group contains _C. gapperi_ and its races, including _caurinus_, and possible other species." Dalquest gave no indication that he had examined any specimens of _caurinus_. When Dalquest (_op. cit._:344) arranged _occidentalis_ and _californicus_ as subspecies of the same species, he used the name combination _Clethrionomys californicus occidentalis_ because he ignored, or was unaware of, the page priority of _occidentalis_ over _californicus_. We regard the anterior position of _occidentalis_ as nomenclatural priority and therefore employ _occidentalis_ rather than _californicus_ as the specific name. Differences between the _gapperi_ group and the _occidentalis_ group include: postpalatal bridge (complete in both groups) truncate posteriorly in the _gapperi_ group and with a median, posteriorly directed, spine in the _occidentalis_ group (this character is not evident in all specimens; some _gapperi_ have a spine, and some _occidentalis_ have the spine much reduced); dentition of the _occidentalis_ group is heavier; enamel pattern of M3 and m1 in _occidentalis_ more simplified--the number of salient and re-entrant angles tends to be reduced in adults of the _occidentalis_ group. An examination of specimens of _caurinus_ (British Columbia: Mt. Seymour, 2 KU; Lund, Malaspina Inlet, 2 USBS; and Inverness, mouth Skeena River, 1 USBS), reveals that, in the presence of the median postpalatal spine and in the characters of the molars, _caurinus_ agrees with the _occidentalis_ group. Clethrionomys occidentalis nivarius (Bailey) 1897. _Evotomys nivarius_ Bailey, Proc. Biol. Soc. Washington, 11:136, May 13, type from northwest slope of Mount Ellinor, 4000 ft., Olympic Mts., Mason County, Washington. The red-backed mouse of the Olympic Peninsula was originally accorded specific rank. Currently it stands in the literature as a subspecies of the wide-spread species _Clethrionomys gapperi_ because Dalquest (Univ. Kansas Publ. Mus. Nat. Hist., 2:343, April 9, 1948) used the name-combination _Clethrionomys gapperi nivarius_. Taylor and Shaw had earlier (Occas. Papers Charles R. Conner Mus., 2:23, 1929) indicated the same status by using the name _Evotomys gapperi nivarius_. Davis (The Recent Mammals of Idaho, The Caxton Printers, Caldwell, Idaho, p. 306, April 5, 1939), however, indicated that the affinities of _nivarius_ were with the _californicus_ [= _occidentalis_] group, although he treated _nivarius_ as a distinct species. We have examined two adult females (K. U. Nos. 10707 and 10708) of _nivarius_ from Reflection Lake, 3800 ft., Jefferson County, Washington, and on the basis of their thick, instead of thin, pterygoid processes concur with Davis that the affinities of _nivarius_ are with the named kinds of _Clethrionomys_ now arranged as subspecies of _Clethrionomys occidentalis_, rather than with the kinds now arranged as subspecies of _Clethrionomys gapperi_. Although we are aware that Dalquest (_op. cit._:101-102) did not find actual intergradation between _nivarius_ and _Clethrionomys occidentalis occidentalis_--a ten-mile gap separated their ranges--we prefer to use the name combination _Clethrionomys occidentalis nivarius_. In doing so we recognize that intergradation ultimately may be found between the two species _C. occidentalis_ and _C. gapperi_; in that event the name _gapperi_ will apply as the name of the species because it has priority over _occidentalis_. The following named kinds of _Clethrionomys_ are considered to be subspecies of _Clethrionomys occidentalis_: CLETHRIONOMYS OCCIDENTALS OCCIDENTALIS (Merriam). 1890. _Evotomys occidentalis_ Merriam, N. Amer. Fauna, 4:25, October 8, type from Aberdeen, Chehalis County, Washington. 1894. _Evotomys pygmaeus_ Rhoads, Proc. Acad. Nat. Sci. Philadelphia, p. 284, October 23, type from mouth of Nisqually River, Pierce County, Washington. 1929. _Evotomys gapperi occidentalis_, Taylor and Shaw, Occas. Papers Charles R. Conner Mus., Washington State College, 2:23. 1948. _Clethrionomys californicus occidentalis_, Dalquest, Univ. Kansas Publ., Mus. Nat. Hist., 2:344, April 9. CLETHRIONOMYS OCCIDENTALIS CALIFORNICUS (Merriam). 1890. _Evotomys californicus_ Merriam, N. Amer. Fauna, 4:26, October 8, type from Eureka, Humboldt County, California. CLETHRIONOMYS OCCIDENTALIS CAURINUS (Bailey). 1898. _Evotomys caurinus_ Bailey, Proc. Biol. Soc. Washington, 12:21, January 27, type from Lund, east shore of Malaspina Inlet, British Columbia. 1935. _Clethrionomys gapperi caurinus_, Racey and Cowan, Rept. British Columbia Prov. Mus. for 1935, p. H 25. CLETHRIONOMYS OCCIDENTALIS MAZAMA (Merriam). 1897. _Evotomys mazama_ Merriam, Proc. Biol. Soc. Washington, 11:71, April 21, type from Crater Lake, 7000 ft., Mount Mazama, Klamath County, Oregon. 1936. _Clethrionomys californicus mazama_, Bailey, N. Amer. Fauna, 55:192, August 29. CLETHRIONOMYS OCCIDENTALIS NIVARIUS (Bailey). 1897. _Evotomys nivarius_ Bailey, Proc. Biol. Soc. Washington, 11:136, May 13, type from northwest slope of Mount Ellinor, 4000 ft., Olympic Mts., Mason County, Washington. CLETHRIONOMYS OCCIDENTALIS OBSCURUS (Merriam). 1897. _Evotomys obscurus_ Merriam, Proc. Biol. Soc. Washington, 11:72, April 21, type from Prospect, 2600 ft., upper Rogue River Valley, Jackson County, Oregon. 1933. _Clethrionomys mazama obscurus_, Grinnell, Univ. California Publ. Zool., 40:185, September 26. 1936. _Clethrionomys californicus obscurus_, Bailey, N. Amer. Fauna, 55:192, August 29. Clethrionomys gapperi pallescens, new name 1940. _Clethrionomys gapperi rufescens_ R. W. Smith, Amer. Midland Nat., 24:233, July, type from Wolfville, Kings County, Nova Scotia (_nec Arvicola rufescens_ de Selys Longchamps, 1836, from Longchamps-sur-Ger, Belgium). The name _rufescens_, as applied by R. W. Smith (Amer. Midland Nat., 24:233, July, 1940) to the red-backed mouse of Nova Scotia, seems to be unavailable under the rules of the International Code of Zoological Nomenclature, since it is a homonym of _Arvicola rufescens_ de Selys Longchamps, 1836, which in turn is a synonym of _Clethrionomys glareolus glareolus_ Schreber, 1780 (Ellerman and Morrison-Scott, Checklist of Palaearctic and Indian Mammals, 1758 to 1946, p. 663, November 19, 1951). Clethrionomys gapperi phaeus (Swarth) 1911. _Evotomys phaeus_ Swarth, Univ. California Publ. Zool., 7:127, January 12, type from Marten Arm, Boca de Quadra, Alaska. When Swarth (_loc. cit._) named the red-backed mouse of the mainland of southern Alaska as a new subspecies, he characterized it as "Size rather large. Differs from _E._ [= _Clethrionomys_] _wrangeli_, nearest it geographically, in cranial characters and in much longer tail; from _E. caurinus_, the species to the southward in British Columbia, in larger size and longer tail." He remarked (_loc. cit._): "I had supposed that the red-backed mouse occurring on the mainland coast of this region would prove to be _E. wrangeli_, but the latter appears to be purely an insular species. I have had no specimens of that race for comparison, but the _Evotomys_ secured differ so widely from it in all the essential peculiarities of the species as given in the published descriptions that there seems little doubt of their belonging to a different species. _Wrangeli_ has a short tail, less than twice as long as the hind foot--in adults of _phaeus_ the tail is invariably more than twice the length of the foot, frequently more than a third of the entire length of the animal." The external and cranial measurements of two subadults in the United States National Museum (No. 217413 from Quadra Lake and No. 217415 from Marten Arm, Boca de Quadra, taken in mid-February) and three old adults from Fort [= Port] Simpson, British Columbia (Nos. 90263-90264, 90272 USBS), are almost the same as those given by Swarth in the original description of _Clethrionomys phaeus_. In cranial measurements, as well as in the structure of the palate and last upper molar, _C. phaeus_ agrees with the _gapperi_ group (to which it has been assigned by Davis, The Recent Mammals of Idaho, The Caxton Printers, p. 306, April 5, 1939, and by Orr, Jour. Mamm., 26:69, February 12, 1945) and differs from _Clethrionomys occidentalis caurinus_ (which was assigned above to the _occidentalis_ group, formerly the _californicus_ group). Since the measurements of specimens examined by us, as well as those recorded by Swarth (_op. cit._), fall within the range of those of the species _Clethrionomys gapperi_, and since the differences between _phaeus_ and _C. g. saturatus_ are of the kind and degree that separate subspecies in _C. gapperi_ we employ the name combination _Clethrionomys gapperi phaeus_ (Swarth). _C. g. saturatus_, as understood by us, occurs to the southeast of _C. g. phaeus_ in the Rocky Mountains of British Columbia, and in northeastern Washington, northern Idaho and northwestern Montana. _Specimens examined._--Total, 23, distributed as follows: Alaska: Chickamin River (Behm Canal), 15 (MVZ); Boca de Quadra, 3 (MVZ); Marten Arm, Boca de Quadra, 1 (USNM); Quadra Lake, 1 (USNM). British Columbia: Fort [= Port] Simpson, 3 (USBS). Clethrionomys gapperi wrangeli (Bailey) 1897. _Evotomys wrangeli_ Bailey, Proc. Biol. Soc. Washington, 11:120, May 13, type from Wrangell, Wrangell Island, Alaska. When Bailey (_loc. cit._) named the red-backed mouse from Wrangell Island, Alaska, he characterized it as "A large, dull-colored species entirely distinct from any known form," and remarked: "In no way does _E._ [= _Clethrionomys_] _wrangeli_ show a close relationship to any other American species. In size and relative proportions it comes closest to _E. dawsoni_, from which it differs widely in coloration and more widely in cranial characters. With the long-tailed species south and east of its range there is no need of comparison." Swarth (Univ. California Publ. Zool., 24:173, June 17, 1922) reported that three specimens from Flood Glacier and 23 from Great Glacier, British Columbia, and four from Sergief Island, at the mouth of the Stikine River, Alaska, were: "All _E. wrangeli_, indistinguishable from specimens at hand from Wrangell Island." Swarth further reported that, although he found no intergradation between _Clethrionomys wrangeli_ from Flood Glacier and the nearly adjacent _Clethrionomys rutilus dawsoni_, "the two species, however, resemble each other so closely in form, and in some pelages in color also, that _wrangeli_ would seem to be a coastal offshoot of _dawsoni_...." Davis (The Recent Mammals of Idaho, The Caxton Printers, p. 306, April 5, 1939) and Orr (Jour. Mamm., 26:69, February 12, 1945) more recently have shown that _Clethrionomys wrangeli_ is not a member of the _rutilus_ group (to which _C. dawsoni_ belongs) but is a member of the _gapperi_ group. Our comparisons of a series of eight topotypes of _wrangeli_ (all in the Biological Surveys Collection) with several subspecies of _Clethrionomys gapperi_ (including _phaeus_, _saturatus_, _galei_, _brevicaudus_, and others) reveal that the differences seen in _wrangeli_ are of the kind and degree that serve to separate subspecies. The red-backed mouse from Wrangell Island, then, should stand as _Clethrionomys gapperi wrangeli_ (Bailey). _Specimens examined._--Total, 31, distributed as follows: Alaska: Wrangell, Wrangell Island, 27 (19 MVZ., 8 USBS); Sergief Island at mouth of Stikine River, 4 (MVZ). Clethrionomys gapperi solus, new subspecies _Type._--Male, adult, skin and skull, No. 74939, Biological Surveys Collection, United States National Museum; from Loring, Revillagigedo Island, Alaska; obtained on September 22, 1895, by C. P. Streator; original No. 4980. _Range._--Known only from two localities on Revillagigedo Island, Alaska. _Diagnosis._--A short-tailed, dark-colored member of the _gapperi_ group. Dorsal stripe wide, between Chestnut and Bay (capitalized color terms after Ridgway: Color Standards and Color Nomenclature. Washington, D. C., 1912), with slight mixture of black-tipped hairs; sides and venter heavily washed with Ochraceous-Tawny. Skull flattened; rostrum proportionately short and wide; auditory bullae relatively uninflated. _Comparisons._--From topotypes of _Clethrionomys gapperi wrangeli_, _C. g. solus_ differs as follows: dorsal stripe wider and slightly brighter; sides brighter; venter more heavily washed with Ochraceous-Tawny (heavy wash in all 13 _C. g. solus_ examined; in _C. g. wrangeli_ no wash in 11, slight wash in 16, and heavy wash in only one); nasals, alveolar extent of upper cheek-teeth and incisive foramina shorter; skull shallower when measured with tympanic bullae included; rostrum averages slightly broader. From _C. g. phaeus_ of the adjacent mainland, _C. g. solus_ differs in: dorsal stripe slightly darker; ventral wash more prominent; tail shorter; skull smaller in all parts measured except that nasals are approximately the same length, auditory bullae notably smaller and teeth notably narrower. _Measurements._--External and cranial measurements of adults are shown in table 1. _Remarks._--Bailey (Proc. Biol. Soc. Washington, 11:120, May 13, 1897) referred 17 specimens from Loring to his newly named species, _E. wrangeli_ [= _Clethrionomys gapperi wrangeli_] but based his description on specimens from Wrangell Island. He pointed out (_loc. cit._) that all of the specimens from Loring had the "bellies strongly washed with buffy-ochraceous, while more than half of those from Wrangell have whitish bellies." _Specimens examined._--Total, 13, all in the Biological Surveys Collection, U. S. National Museum, from the following localities: Alaska: Revillagigedo Island: Loring, 10; mouth of Fish Creek, Ketchikan, 3. Clethrionomys gapperi stikinensis, new subspecies _Type._--Male, adult, skin and skull, No. 30735, Museum of Vertebrate Zoology, University of California; from Stikine River at Great Glacier, British Columbia; obtained on August 13, 1919, by J. Dixon; original number 7691. _Range._--Known only from the lower Stikine River Valley of British Columbia and the Cleveland Peninsula of Alaska. _Diagnosis._--A medium-sized, dark-colored member of the _gapperi_ group. Dorsal stripe wide, near Auburn with mixture of black-tipped hairs; sides and venter washed with Ochraceous-Tawny. Skull small; cheek-teeth narrow; auditory bullae relatively uninflated. _Comparisons._--From topotypes of _Clethrionomys gapperi wrangeli_, _C. g. stikinensis_ differs as follows: dorsal stripe slightly wider and brighter; sides slightly duller (lacking the olivaceous wash of _C. g. wrangeli_); all cranial measurements taken averaging smaller except height of skull, which is approximately the same; alveolar length of upper tooth-row and length of incisive foramina notably shorter; auditory bullae less inflated; cheek-teeth much narrower. From topotypes of _C. g. phaeus_, _C. g. stikinensis_ differs as follows: dorsal stripe and sides darker; auditory bullae less inflated; cheek-teeth narrower; skull smaller in most measurements taken (see table 1). From topotypes of _C. g. solus_, _C. g. stikinensis_ differs as follows: dorsal stripe lighter (more tawny underwash); ventral wash of buffy much paler (especially noticeable around mouth and on throat); zygomatic and lambdoidal breadths greater; skull deeper; auditory bullae more inflated; cheek-teeth slightly heavier. TABLE 1. _External and cranial measurements of Clethrionomys._ N | | | | | | | | | | | u | | | | | | | | | | | m | | | | | | | | | | L | b | | | | | | | | | | e | e | | | | | | | | | | n | r s | | | | | | | | | | g | e | | | | | | | | | | t | o x | | | | | | | | | | h | f | | | | C | | | | | | | o | | | | o | | | | | | o | i r | | | | n | | | | | | f | n | | | | d | | L | | A | B | | d s | | | | y | Z | a | | l | r | i | i p | | | | l | y | m | L | v | e | n | v e | | | | o | g | b | e | e u| a | c | H i c | | | | b | o | d | n | o p| d | i | e d i | | | | a | m | o | g | l p| t | s | i u m | T | | | s | a | i | t | a e| h | i | g a e | o | | | i | t | d | h | r r| | v | h l n | t | | | l | i | a | | | o | e | t s | a | | H | a | c | l | o | l t| f | | m | l | | i | r | | | f | e o| | f | o o e | | | n | | b | b | | n o| r | o | f f a | l | | d | l | r | r | n | g t| o | r | s | e | | | e | e | e | a | t h| s | a | s e u | n | T | f | n | a | a | s | h | t | m | k a r | g | a | o | g | d | d | a | r| r | i | u c e | t | i | o | t | t | t | l | o o| u | n | l h d | h | l | t | h | h | h | s | f w| m | a | l _Clethrionomys gapperi solus_, Loring Male type |133|33 |20 | 22.3 | 12.5 |10.9 |6.8 |5.1 |3.4 |5.3 | 9.0 Male 5 av. |131|34 |20 | 22 | 12.7 |10.8 |6.8 |5.3 |3.5 |5.1 | 9.1 min.|128|33 |19 | 21.8 | 12.5 |10.5 |6.7 |5.1 |3.3 |5.0 | 8.9 max.|133|36 |20 | 22.3 | 13.0 |11.2 |7.1 |5.5 |3.6 |5.3 | 9.5 Female 5 av. |128|34 |19 | 21.3 | 12.5 |10.5 |6.5 |5.4 |3.5 |4.9 | 9.2 min.|124|31 |19 | 20.9 | 12.3 |10.3 |6.0 |5.2 |3.3 |4.8 | 8.9 max.|140|36 |20 | 21.7 | 12.7 |10.7 |7.0 |5.6 |3.6 |5.0 | 9.5 _Clethrionomys gapperi stikinensis_, Stikine River at Great Glacier Male type |145|39 |20 | 23.2 | 13.9 |11.4 |7.3 |5.0 |3.1 |5.5 | 9.5 Male 4 av. |136|35 |20 | 22.2 | 13.0 |11.1 |6.8 |5.2 |3.4 |5.2 | 9.4 min.|132|33 |19 | 21.5 | 12.3 |10.7 |6.5 |5.0 |3.1 |5.1 | 9.1 max.|145|39 |20 | 23.2 | 13.9 |11.4 |7.3 |5.6 |3.5 |5.5 | 9.7 Female 7 av. |134|33 |19 | 21.8 | 12.7^6*|10.9 |7.0 |5.4 |3.4 |5.1 | 9.5 min.|125|30 |19 | 21.5 | 12.5 |10.5 |6.7 |5.3 |3.2 |5.0 | 9.2 max.|147|35 |20 | 22.2 | 12.9 |11. |7.1 |5.6 |3.7 |5.3 | 9.8 _Clethrionomys gapperi wrangeli_, Wrangell Male 9 av. |139|36 |19 | 23.4^8| 13.3 |11.4^8 |7.3 | .6 | .6 | .6 | 9.6^8 min.|130|31 |18 | 22.9 | 13.0 |10.9 |7.1 |5.5 |3.3 |5.4 | 9.2 max.|151|43 |20 | 23.9 | 13.7 |11.8 |7.6 |5.8 |4.0 |5.8 |10.1 Female 16 av.|134|34 |18^15| 23.2 | 13.3 |11.2^13|7.3 |5.8 |3.5 |5.5 | 9.4 min.|123|28 |17 | 22.4 | 12.6 |10.7 |6.9 |5.5 |3.2 |5.2 | 9.0 max.|156|45 |20 | 24.1 | 14.1 |11.8 |8.0 |6.1 |3.7 |5.9 | 9.7 _Clethrionomys gapperi phaeus_, Chickamin River Male 5 av. |148|47 |20 | 23.0^4| 13.7^4|11.3^4 |7.5^4|5.3^4|3.5^4|5.3^4| 9.7^3 min.|138|38 |20 | 22.3 | 13.0 |11.1 |7.1 |5.3 |3.4 |4.9 | 9.3 max.|159|51 |21 | 23.8 | 14.6 |11.8 |7.7 |5.6 |3.8 |5.6 |10.0 Female 4 av. |153|49 |20 | 23.1^3| 13.4 |11.2^3 |7.6^3|5.2 |3.7 |5.3 | 9.6^3 min.|140|44 |20 | 22.4 | 12.8 |10.8 |7.3 |5.0 |3.4 |5.1 | 9.2 max.|164|56 |20 | 24.2 | 13.6 |11.4 |7.7 |5.3 |3.9 |5.5 | 9.8 *Superior numbers denote the number of individuals averaged. _Measurements_.--External and cranial measurements of adults are given in table 1. _Remarks_.--Morphologically _C. g. stikinensis_ shows greater resemblance to _C. g. solus_ of Revillagigedo Island, than to the geographically adjacent subspecies _C. g. wrangeli_ and _C. g. phaeus_. Possibly the original stock of _C. g. solus_ was rafted to Revillagigedo Island from the Cleveland Peninsula. _Specimens examined_.--Total, 29, all in the Museum of Vertebrate Zoology, University of California, distributed as follows: British Columbia: Stikine River at Great Glacier, 22; Stikine River at Flood Glacier, 3. Alaska: Bradfield Canal, 1; Helm Bay, 2. Pitymys pinetorum scalopsoides (Audubon and Bachman) 1841. _Arvicola scalopsoides_ Audubon and Bachman, Proc. Acad. Nat. Sci. Philadelphia, 1:97, type from Long Island, New York. 1912. _Pitymys pinetorum scalopsoides_ Miller, U. S. Nat. Mus. Bull., 79:229, December 31. Hanson (Trans. Wisconsin Acad. Sci., Arts, and Letters, 36:124, 1944) reported two pine mice from near Prairie du Sac, in Westpoint Township, Columbia County, Wisconsin, as _Pitymys pinetorum scalopsoides_ but cast doubt upon their subspecific identity. He also reported pine mice from Blue Mounds, Dane County, Wisconsin. We have examined these specimens (Westpoint, Columbia County, 2--No. 544, skin only, UWDEZ, and No. 521, skin only, H. C. Hanson's private collection; Westpoint, Dane County, 1, No. 11620, UWZM; Vermont, Dane County, 2, Nos. 11674 and 11694, UWZM) and have compared them with topotypes of _P. p. schmidti_, and with specimens of _P. p. nemoralis_ and _P. p. scalopsoides_. The specimens from Columbia and Dane counties differ from _P. p. schmidti_ in the greater zygomatic breadth, and lesser height of skull. They differ from _P. p. nemoralis_ of comparable age in shorter tooth-row and generally smaller skull. The interorbital region, however, is wider. In all of the features mentioned above, the specimens in question agree with _Pitymys pinetorum scalopsoides_, to which subspecies they are here referred. Microtus pennsylvanicus aztecus (Allen) 1893. _Arvicola (Mynomes) aztecus_ Allen, Bull. Amer. Mus. Nat. Hist., 5:73, April 28, type from Aztec, 5900 ft., San Juan County, New Mexico. Allen (_loc. cit._) described this species on the basis of two specimens from Aztec, New Mexico, and three from La Plata, New Mexico. He characterized it as "Size large; pelage very full and soft; tail short; skull very narrow. "Above grayish brown with a tinge of pale buff; fur blackish plumbeous beneath the surface, tipped with pale yellowish brown, and varied with longer, projecting, black-tipped hairs; below grayish white, the fur plumbeous beneath the surface and tipped with white, giving a whitish gray effect. Feet dusky; tail dusky brown above, dull white below." Allen identified as this species "a large _Arvicola_ from Estes Park, Colorado, which I have before been unable to allocate. I am unable to find that it differs in any particular from the specimens from New Mexico." He pointed out also (_op. cit._:73-74) that "The type and only positively identified specimen of Baird's _Arvicola modesta_ [= _Microtus pennsylvanicus modestus_ (Baird)] from Sawatche Pass, Colorado, is a very young specimen in poor condition. An examination of a series of adult and young examples from the type locality will be necessary in order to determine its relationships to _A. alticolus_ [= _Microtus longicaudus alticolus_ (Merriam)] and _A. aztecus_." Bailey, in his revision of the American voles of the genus _Microtus_ (N. Amer. Fauna, 17:20), showed _Arvicola modesta_ Baird to be a subspecies of _Microtus pennsylvanicus_ but retained _Microtus aztecus_ (Allen) as a distinct species. In describing _M. aztecus_ he wrote "the size similar to _M. pennsylvanicus_, but with shorter tail and larger hindfoot; skull long; braincase narrow; interparietal long ..." and remarked that "_Microtus aztecus_ belongs to the _pennsylvanicus_ group. Externally it is not very different from _modestus_, but none of the specimens show any signs of intergradation; and the skull characters are so well marked that there seems no doubt of its full specific rank." Subsequent to the publication of Allen's (_op. cit._) account and Bailey's account (_op. cit._), additional material was collected that helps to clarify the relationships of _Microtus aztecus_. A comparison of six adult topotypes of _Microtus aztecus_ with a series of nine adults of _M. p. modestus_ from 1 mi. S, 2 mi. E Eagle Nest, 8100 ft., Colfax County, New Mexico, with three adults from 1-1/2 mi. E Manassa, Conejos County, Colorado, and with four adults from Saguache County, Colorado (all in KU), reveals that the supposed "well marked" external and cranial differences between the two forms are not nearly so evident as was indicated by Bailey. The cranial differences that exist between these two forms (narrower nasals, slightly longer interparietal, slightly longer and narrower skull in _aztecus_) are evident only as averages. Although geographically intermediate specimens are lacking, the morphological differences between the two kinds of animals are of the degree and kind that separate subspecies, rather than species. We therefore judge _M. aztecus_ (Allen) to be only subspecifically distinct from _M. pennsylvanicus modestus_ and employ the name _Microtus pennsylvanicus aztecus_. Microtus pennsylvanicus funebris (Dale) 1940. _Microtus pennsylvanicus funebris_ Dale, Jour. Mamm., 21:338, August 14, type from Coldstream, 1450 ft., 3-1/2 mi. SE Vernon, British Columbia. Taylor and Shaw (Occas. Papers Charles R. Conner Mus., State College Washington, 2:24, December, 1929) list under _Microtus nanus_ [= _montanus_] _canescens_ material from Calispell Peak, Washington. Probably the basis for this record is a specimen in the Biological Surveys collection (adult male, 236474) taken on May 9, 1921, by G. G. Cantwell, and labelled as Calispell Peak, 9 mi. W Locke, 3500 ft., Pend Oreille County. An examination (by Hall and Kelson) of the specimen discloses that it is of the species _Microtus pennsylvanicus_, and that it falls within the geographic range ascribed to the subspecies _Microtus pennsylvanicus funebris_ by Dalquest (Univ. Kansas Publ., Mus. Nat. Hist., 2:346, April 9, 1948). Microtus oeconomus amakensis (Murie) 1930. _Microtus amakensis_ Murie, Jour. Mamm., 11:74, February 11, type from Amak Island, Bering Sea, Alaska. When Murie (Jour. Mamm., 11:75, February 11, 1930) named the meadow mouse from Amak Island, Alaska, as _amakensis_, he arranged it as a separate species. One of us (Hall) and K. R. Kelson examined the type and topotypes of _amakensis_ in the Biological Surveys collection in the U. S. National Museum and compared them with series of _Microtus oeconomus operarius_, _M. o. sitkensis_, _M. o. elymocetes_, _M. o. yakutatensis_, and _M. o. kadiacensis_. Among the specimens examined of the latter subspecies were 17 from Izambek Bay, Kodiak Peninsula, on the mainland opposite Amak Island, the type locality of _amakensis_. The characters given by Murie (_op. cit._) serve to separate _amakensis_ from closely related neighboring kinds of meadow mice, but are of the degree and kind that, in this group of meadow mice, separate subspecies rather than species. Although actual intergrades are lacking, the animals from Amak Island are considered to be only subspecifically distinct and to belong to the _oeconomus_ complex. The name _Microtus oeconomus amakensis_ is applied to them. Microtus longicaudus mordax (Merriam) 1891. _Arvicola_ (_Mynomes_) _mordax_ Merriam, N. Amer. Fauna, 5:61, July 30, type from Sawtooth (= Alturas) Lake, 7200 ft., east base of Sawtooth Mountains, Blaine County, Idaho. 1938. _Microtus longicaudus mordax_, Goldman, Jour. Mamm., 19:491, November 14. Dalquest (Univ. Kansas Publ., Mus. Nat. Hist., 2:353, April 9, 1948) assigned all the meadow mice of the species _Microtus longicaudus_ from approximately the eastern half of Washington State to _Microtus longicaudus halli_ Hayman and Holt and, in doing so, excluded the subspecies _Microtus longicaudus mordax_ from that state. This assignment of specimens in Washington had the effect of separating the geographic range of _M. l. mordax_ into two parts. One part was in south-central British Columbia and the other part was mainly in the Rocky Mountain region of the United States. Hall and Kelson examined specimens in the Biological Surveys collection in the U. S. National Museum in an attempt to determine more precisely the ranges of the subspecies in southern Canada, Washington, and Idaho. _Microtus longicaudus angustus_ [= _M. l. halli_] was described by one of us (Hall, Univ. California Publ. Zool., 37:13, April 10, 1931) as differing from _mordax_ in narrower braincase, higher skull near the anterior end of the frontals, darker coloration, and seemingly smaller size. After examining the material in the U. S. National Museum no reason is seen at the present time to amend this characterization, except to add that some specimens of _M. l. mordax_ are as dark as seasonably comparable specimens of _M. l. halli_. Examination of specimens of _Microtus longicaudus_ from Washington east of the Cascade Range (those from the Blue Mountain area excepted) discloses that the skulls do not differ essentially from those of topotypes of _M. l. mordax_, but do differ, as outlined above, from near-topotypes of _M. l. halli_. There is considerable variation in color among the Washington-taken specimens of _Microtus longicaudus_. Animals from the eastern flanks of the Cascades average darker than those taken, north of the Snake River, still farther east in Washington. Possibly Dalquest (_op. cit._) relied mainly upon this darker color in assigning the specimens from eastern Washington to _M. l. halli_. Relying principally upon cranial characters, we conclude that most of the specimens are better referred to _M. l. mordax_ and that _M. l. halli_ is restricted, in Washington, to the Blue Mountains. _Specimens examined of Microtus longicaudus mordax._--Total, 74, all in the Biological Surveys Collection, distributed as follows: Washington: _Okanogan_ _County_: mouth of Holmar Creek, W Fork Paysaten River, 4700 ft., 1; Conconully, 3; Twisp, 1; Omak Lake, 1200 ft., 3. _Stevens County_: 5 mi. N Colville, 1. _Pend Oreille County_: 9 mi. N Metalina, 2600 ft., 1; Sullivan Lake, 3000 ft., 3. _Chelan County_: Sethekin, 1079 ft., 3; head of Lake Chelan, 900 ft., 12; Hart Lake, Railroad Creek, 3900 ft., 1; Entiat, 20 mi from mouth of Entiat River, 1680 ft., 13; Wenatchee, 4. _Douglas County_: Waterville, 1. _Jefferson County_: Cleveland, 2. _Kittitas County_: 2 mi. S Blewett Pass, 3000 ft., 6: Ellensburg, 1500 ft., 4. _Whitman County_: Colfax, 2. _Yakima County_: McAllister Meadows, Tieton River, 3000 ft., 3; Gotchen Cr., 5500 ft., near Sava Spring, Mt. Adams, 2. _Klickitat County_: 8 mi. S Glenwood, base Mt. Adams, 2. _Asotin County_: Anatone, 3300 ft., 4; Bly, 1000 ft., 2. Microtus miurus muriei (Nelson) 1931. _Microtus muriei_ Nelson, Jour. Mamm., 12:311, August 24, type from Kutuk River (tributary of Alatna River), Endicott Mts., Alaska. Rausch (Jour. Washington Acad. Sci., 40:135, April 21, 1950) proposed the name _Microtus miurus paneaki_, with type locality at Tolugak Lake (lat. 68° 24' N, long. 152° 10' W), Brooks Range, Alaska, for a meadow mouse of the subgenus _Stenocranius_. This place is only approximately forty miles east and north of the type locality of the earlier named _Microtus muriei_, also a member of the subgenus _Stenocranius_. Large series of specimens of this subgenus, from the Arctic Slope of Alaska, are in the Museum of Natural History of the University of Kansas. Study of these indicates that the differences, which Rausch (_op. cit._:136) described as distinguishing his _M. m. paneaki_ from _M. muriei_, result from differences in age of the specimens, and possibly in part from differences in seasonal condition of pelage. For example, Rausch thought that _M. m. paneaki_ was larger than _M. muriei_ but our specimens reveal that such is not the case. The measurements given below of the type specimen of _M. muriei_ (after Nelson, original description) and measurements (in parentheses) of an immature female (43807 K. U.) of _Microtus miurus muriei_ from Chandler Lake, 68° 12', 152° 45', 2900 ft., Alaska, show close correspondence in size. Total length, 119 (122); tail vertebrae, 24 (24); hind foot, 20 (20); condylobasal length, 24.3 (24.5); zygomatic breadth, 10.7 (11.0); greatest width of braincase, 9.0 (9.0); length of nasals, 6.5 (6.0); basal width of rostrum, 4.0 (4.3). In the light of all of the evidence now available, it seems best to treat _Microtus miurus paneaki_ Rausch as a synonym of _Microtus muriei_ Nelson. Quay (Jour. Mamm., 32:95, February 15, 1951) identified fifty-eight specimens from the Seward Peninsula of Alaska as _Microtus miurus oreas_ Osgood. Through the courtesy of Dr. Charles P. Lyman, fifteen of Quay's specimens in the Museum of Comparative Zoology at Harvard College have been examined by one of us (Hall). These specimens are as follows: Lava Lake (43378, 43379, 43381, 43382, 43386, 43467 and 43478); Mt. Boyan (43384, 43385, 43463 and 43477); Anvil Hill [= Peak], Cooper Gulch (43377, 43464 and 43473); ----? Lake, 43383. Although we are not prepared to say that these specimens are _M. m. muriei_, they seem to resemble _M. m. muriei_ as closely as they do any other named form and we here refer them to that subspecies. The facts are that a critical taxonomic study of the American specimens of the subgenus _Stenocranius_ is required in order to ascertain the geographic variation. One of us (Hall) has examined the holotypes of the kinds named from Alaska, and the material listed by R. Baker (Univ. Kansas Publ. Mus. Nat. Hist., 5:109) of the two kinds named from Canada. The degree and nature of the variation shown by these specimens lead us to the conclusion that all are of a single species. If the American mouse is specifically distinct from any of the previously named Asiatic species--at this writing we lack material to decide this question--the named kinds from the mainland of the New World may stand as follows: MICROTUS MIURUS ANDERSONI Rand. 1945. _Microtus andersoni_ Rand, Bull. Nat. Mus. Canada, 99:42, prior to June 20, type from near headwaters of Little Keel River, 5500 ft., 82 mi. W Mackenzie River on Canol Road, Mackenzie. MICROTUS MIURUS CANTATOR Anderson. 1947. _Microtus cantator_ Anderson, Bull. Nat. Mus. Canada, 102:161, January 24, type from mountain top near Tepee Lake, 61° 35' N, 140° 22' W, N slope Elias Range, Yukon Terr. MICROTUS MIURUS MIURUS Osgood. 1901. _Microtus miurus_ Osgood, N. Amer. Fauna, 21:64, September 26, type from head of Bear Creek, in mts. near Hope City, Turnagain Arm, Cook Inlet, Alaska. MICROTUS MIURUS MURIEI Nelson. 1931. _Microtus muriei_ Nelson, Jour. Mamm., 12:311, August 24, type from Kutuk River (tributary of Alatna River), Endicott Mts., Alaska. 1950. _Microtus miurus paneaki_ Rausch, Jour. Washington Acad. Sci., 40:135, April 21, type from Tolugak Lake (lat. 68° 24' N, long. 152° 10'), Brooks Range, Alaska. MICROTUS MIURUS OREAS Osgood. 1907. _Microtus miurus oreas_ Osgood, Proc. Biol. Soc. Washington, 20:61, April 18, type from Toklat River, Alaskan Range, Alaska. _Transmitted July 8, 1952._ *** END OF THE PROJECT GUTENBERG EBOOK COMMENTS ON THE TAXONOMY AND GEOGRAPHIC DISTRIBUTION OF NORTH AMERICAN MICROTINES *** 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. 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