E. RAYMOND HALL and KEITH R. KELSON

In preparing maps showing the geographic distribution of North American

mammals we have found in the literature conflicting statements and

questionable identifications, which have led us to examine the

specimens concerned with results as set forth below. Our studies have

been aided by a contract (NR 161-791) between the Office of Naval

Research, Department of the Navy, and the University of Kansas.

Grateful acknowledgment is made to the persons in charge of the several

collections of mammals consulted for permission to examine and study

the specimens therein.

~Didelphis marsupialis californica~ Bennett

From Cuernavaca, Morelos, Hooper (Jour. Mamm., 28:43, February 1, 1947)

lists a specimen, as he says, on purely geographic grounds, as of the

subspecies _Didelphis mesamericana tabascensis_. We have examined this

specimen, an unsexed skull-only, which falls within the range of

individual variation of _Didelphis marsupialis californica_ and refer

the specimen to that subspecies.

~Didelphis marsupialis etensis~ J. A. Allen

From El Muneco, Costa Rica, Harris (Occas. Papers, Mus. Zool. Univ.

Michigan, no. 476:7, October 8, 1943) lists as _Didelphis richmondi_ a

specimen ([Male], No. 67550 U.M.). Our examination of the specimen

shows it to be within the range of individual variation of populations

that have been referred to _D. m. etensis_ from adjoining areas. We

identify the specimen as _Didelphis marsupialis etensis_.

~Didelphis marsupialis tabascensis~ J. A. Allen

From Minatitlan, Veracruz, J. A. Allen (Bull. Amer. Mus. Nat. Hist.,

14:168, June 15) listed a specimen under the name _Didelphis

marsupialis_ [in the trinomial sense] instead of under the name

_Didelphis marsupialis tabascensis_, which would be expected, on

geographic grounds, to apply. The specimen is No. 78123, U.S. Nat.

Mus., Biol. Surv. Coll. Our examination of the specimen reveals that it

is within the range of individual variation of _Didelphis marsupialis

tabascensis_ and we identify the specimen as of that subspecies. From

Yaruca, Honduras, Bangs (Bull. Mus. Comp. Zool., 39:157, July, 1903)

doubtfully listed as _Didelphis yucatanensis_ a specimen, No. 10611,

M.C.Z. Our examination of the specimen indicates that it is within the

range of variation expectable in _Didelphis marsupialis tabascensis_,

known from surrounding areas, and we identify the specimen as

_Didelphis marsupialis tabascensis_.

~Didelphis marsupialis virginiana~ Kerr

J. A. Allen (Bull. Amer. Mus. Nat. Hist., 14:166, May 28, 1901) and A.

H. Howell (N. Amer. Fauna, 45:20, October 28, 1921) have identified

four skulls from Sylacuga, Alabama, as _Didelphis virginiana pigra_.

The two subspecies _virginiana_ and _pigra_ are not known to differ

cranially. We have, however, examined the skulls which are Nos.

44057-44060 in the U.S. Nat. Mus., Biol. Surv. Coll. Because they are

from a place north of other localities (Auburn and Greensboro, Alabama)

from which the subspecies _virginiana_ has been recorded, and within

the geographic range of _virginiana_, we identify the specimens as

_Didelphis marsupialis virginiana_.

Sycamore Creek (synonymous with Fort Worth), Texas, is a place from

which J. A. Allen (_op. cit._:173) recorded a specimen as _Didelphis

marsupialis texensis_. This specimen (No. 24359/31765 U. S. Nat. Mus.,

Biol. Surv. Coll.) is in the black color-phase. There are only a few

white hairs on the hind feet, and the basal fourth of the tail is

black. The black phase occurs all through the range of the species _D.

marsupialis_ and our examination of the specimen reveals no characters

by which it can be distinguished from _D. m. virginiana_ of the

surrounding region and we accordingly identify the specimen as

_Didelphis marsupialis virginiana_.

~Didelphis marsupialis pigra~ Bangs

Davis (Jour. Mamm., 25:375, December 12, 1944) was one writer who

presented evidence that _Didelphis virginiana_ (through its subspecies

_virginiana_ or _pigra_ or both) was only subspecifically distinct from

the species _Didelphis mesembrinus_ (= _D. marsupialis_) through the

subspecies _texensis_. Davis, however, did not actually employ a name

combination that would enforce his conclusion and he remarked that he

had not seen specimens which showed actual intergradation in the color

of the toes. As the remarks below will show, Davis (_loc. cit._) was

correct in his supposition that J. A. Allen had seen such specimens.

Deming Station, Matagordo, and Velasco, Texas, are three places from

which J. A. Allen (Bull. Amer. Mus. Nat. Hist., 14:162, May 28, 1901)

listed specimens as _Didelphis virginiana_. The specimens concerned are

in the Biological Surveys Collection of the U.S. Nat. Museum and bear

catalogue numbers as follows: Deming Station, 32430/44266, 32432/44268,

32433/44269; Matagordo, 32431/44267; Velasco, 32812/44833. In each

specimen the tail is shorter than the head and body. The specimen from

Velasco is semi-black, has the basal tenth of the tail black and there

is no white on the ears or tail. The specimen from Matagordo is

grayish, has the basal fifth of the tail black, ears black, the right

hind foot black, but there is some white on the toes of the left hind

foot and on each of the forefeet. Of the three specimens from Deming

Station, all are in the gray color-phase. The first has the tail black

only as far from the base as there is hair and there is considerable

whitish on the hind toes. The second specimen has the basal fifth of

the tail black and a slight amount of whitish on the hind toes. The

third specimen has the basal third of the tail black and the toes are

all black. In the sum total of their characters the specimens mentioned

above are referable to _Didelphis marsupialis pigra_. These five

specimens, and indeed the three from Deming Station alone, show

intergradation in coloration of the feet between _Didelphis marsupialis

texensis_ and _Didelphis virginiana pigra_. Probably there is three-way

intergradation here at Deming Station in that _D. v. virginiana_

immediately to the north is involved. The specimens mentioned above,

along with the information recorded by Davis (_loc. cit._) and other

authors (for example, J. A. Allen, _loc. cit._, and Bull. Amer. Mus.

Nat. Hist., 16:249-279, August 18, 1902), give basis for arranging the

North American _Didelphis_ as follows:

_Didelphis marsupialis virginiana_ Kerr.

1792. _Didelphis virginiana_ Kerr, Animal Kingdom, p. 193, type

locality Virginia.

_Didelphis marsupialis pigra_ Bangs.

1898. _Didelphis virginiana pigra_ Bangs, Proc. Boston Soc.

Nat. Hist., 28:172, March, type from Oak Lodge, opposite Micco,

Brevard Co., Florida.

_Didelphis marsupialis texensis_ J. A. Allen.

1901. _Didelphis marsupialis texensis_ J. A. Allen, Bull. Amer.

Mus. Nat. Hist., 14:172, June 15, type from Brownsville,

Cameron County, Texas.

_Didelphis marsupialis californica_ Bennett.

1833. _Didelphis Californica_ Bennett, Proc. Zool. Soc. London,

p. 40, May 17, type probably from northwestern part of present

Republic of Mexico.

1924. _Didelphis mesamericana mesamericana_, Miller. Bull. U.S.

Nat. Mus., 128:3, April 29, 1924, and authors. Type locality,

northern Mexico. (_Did[elphys]. mesamericana_ Oken, Lehrbuch d.

naturgesch., pt. 3, vol. 2, p. 1152, 1816, along with other

names from Oken 1816, is judged to be unavailable under current

rules of zoological nomenclature.)

_Didelphis marsupialis tabascensis_ J. A. Allen.

1901. _Didelphis marsupialis tabascensis_ J. A. Allen, Bull.

Amer. Mus. Nat. Hist., 14:173, June 15, type from Teapa,

Tabasco.

_Didelphis marsupialis yucatanensis_ J. A. Allen.

1901. _Didelphis yucatanensis_ J. A. Allen, Bull. Amer. Mus.

Nat. Hist., 14:178, June 15, type from Chichenitza, Yucatan.

_Didelphis marsupialis cozumelae_ Merriam.

1901. _Didelphis yucatanensis cozumelae_ Merriam, Proc. Biol.

Soc. Washington, 14:101, July 19, type from Cozumel Island,

Yucatan.

_Didelphis marsupialis richmondi_ J. A. Allen.

1901. _Didelphis richmondi_ J. A. Allen, Bull. Amer. Mus. Nat.

Hist., 14:175, June 15, type from Greytown, Nicaragua.

1920. _D[idelphis], m[arsupialis], richmondi_, Goldman,

Smithsonian Misc. Coll., 69(5):46, April 24.

_Didelphis marsupialis etensis_ J. A. Allen.

1902. _Didelphis marsupialis etensis_ J. A. Allen, Bull. Amer.

Mus. Nat. Hist., 16:262, August 18, type from Eten, Piura,

Peru.

_Didelphis marsupialis battyi_ Thomas.

1902. _Didelphis marsupialis battyi_ Thomas, Novitates

Zoologicae, 9:137, April 10, type from Coiba Island, Panama.

_Didelphis marsupialis particeps_ Goldman.

1917. _Didelphis marsupialis particeps_ Goldman, Proc. Biol.

Soc. Washington, 30:107, May 23, type from San Miguel Island,

Panama.

_Didelphis marsupialis insularis_ J. A. Allen.

1902. _Didelphis marsupialis insularis_ J. A. Allen, Bull.

Amer. Mus. Nat. Hist., 16:259, August 18, type from Caparo,

Trinidad.

In listing the subspecific names given immediately above we are aware

of the possibility that a thorough study of the geographic variation in

_Didelphis marsupialis_ may contract or expand the list of recognizable

subspecies. We are aware also that Hershkovitz (Fieldiana: Zoology, 31

(No. 47):548, July 10, 1951) has arranged several of the subspecific

names listed immediately above as synonyms of _Didelphis marsupialis

californica_ Bennett. We have not employed his arrangement because he

has not given proof that the currently recognized subspecies are

indistinguishable.

~Caluromys derbianus canus~ (Matschie)

Matschie (Sitzungsberichte der Gesellschaft Naturforschender Freunde zu

Berlin, Jahrgang 1917, p. 284 (for April), September, 1917) applied the

name _Micoureus canus_ to a specimen on which the locality was no more

precise than Nicaragua. Comparison of Matschie's description with

specimens in the United States National Museum (including the holotype

of _Philander centralis_ Hollister and referred specimens of _Philander

laniger pallidus_ Thomas) reveals that Matschie's specimen was

intermediate in coloration between the other two kinds of woolly

opossums named above and that there is nothing distinctive, in the

specific sense, in the cranial measurements which Matschie published

(_op. cit._). _M. canus_, therefore, may be merely an intergrade

between the two previously named woolly opossums (_C. d. centralis_ and

_C. d. pallidus_), an individual variant of a previously named kind,

say, _C. d. pallidus_, or a valid subspecies. If it is a recognizable

subspecies, it probably comes from somewhere in the eastern half of

Nicaragua. As a means of handling the name, _Micoureus canus_ Matschie,

we tentatively place it as a subspecies of the species _Caluromys

derbianus_. The name may, therefore, stand as _Caluromys derbianus

canus_ (Matschie), with type locality in Guatemala.

~Caluromys derbianus fervidus~ (Thomas)

Elliott (Field Columb. Mus. Nat. Hist., Publ. No. 115, Zool. Ser., 8:5,

1907) lists as _Caluromys laniger pallidus_ a specimen from Honduras

that was acquired for the Field Columbian Museum (= Chicago Natural

History Museum) by purchase from Ward's Natural Science Establishment

of Rochester, New York. On August 4, 1951, in the Chicago Natural

History Museum, we found in the catalogue of the collection of Recent

mammals an entry for a male _Caluromys_ bearing catalogue number 6 and

listed as from "San Pedro Sula [Honduras]. From Wards. Mounted". In the

collection of study specimens there is no specimen from Honduras that

was purchased from Ward's, mounted or unmounted. In the sealed,

glass-fronted, exhibit cases of mammals on display there is one, and

only one, _Caluromys_. It is presumed to be specimen No. 6. This

specimen is not _C. d. pallidus_ because it is too dark. It could be

_Caluromys derbianus fervidus_ and we tentatively refer it to that

subspecies.

~Caluromys derbianus pallidus~ (Thomas)

From Puntarenas, Costa Rica, Harris (Occas. Papers Mus. Zool. Univ.

Michigan, 476:7, October 8, 1943) listed as _Caluromys laniger

centralis_ a female, skull and skin, No. 62702 in the Museum of Zoology

of the University of Michigan. We have examined this specimen, the

color of which is darker than in some other specimens of _C. d. pallidus_

but lighter than that of specimens of _C. d. centralis_ (for example,

specimens from Turrialba, Costa Rica) and on basis of color we refer No.

62702 to _Caluromys derbianus pallidus_.

~Scalopus aquaticus aereus~ (Bangs)

Bangs' (Proc. Biol. Soc. Washington, 10:138, December 28, 1896) name

_S. a. aereus_ was based on a single specimen that shows more than an

average amount of coppery color. Jackson (N. Amer. Fauna, 38:52,

September 30, 1915) and subsequent authors accord full specific rank to

the specimen under the name _Scalopus aereus_. Blair (Amer. Midland

Nat., 22:98, July, 1939) recorded, from the type locality of _Scalopus

aereus_, normally colored individuals of _Scalopus aquaticus pulcher_

Jackson. Previously, Scheffer (Kansas State Agric. College, Exp. Bull.,

168:4, August 1, 1910) reported that in his examination of 100

individuals of _Scalops_ [= _Scalopus_] _aquaticus_ from Manhattan,

Kansas, there were two individuals "that were suffused all over with

rich golden brown." Because our examination of the type specimen of

_Scalops texanus aereus_ Bangs reveals no features additional to

coppery color that differentiate _aereus_ from other individuals of

_Scalopus aquaticus pulcher_ Jackson (Proc. Biol. Soc. Washington,

27:19, February 2, 1914) we conclude that Jackson's name and Bangs'

name (_Scalops texanus aereus_) apply to the same subspecies. Bangs'

name has priority and the correct name, therefore, for the populations

of moles that in recent years have been designated as _Scalopus aereus_

Bangs and _Scalopus aquaticus pulcher_ Jackson will be _Scalopus

aquaticus aereus_ (Bangs). This name combination was previously used by

Miller (U.S. Nat. Mus. Bull., 79:8, December 31, 1912).

~Scalopus aquaticus australis~ (Chapman)

Quay (Jour. Mamm., 30:66, February 14, 1949) recorded _Scalopus

aquaticus_ from Springhill Plantation, 10 miles south-southwest of

Thomasville, Georgia. He stated that the specimens were intermediate

between the subspecies _S. a. australis_ and _S. a. howelli_, but did

not refer the specimens to either subspecies. The locality whence the

material was obtained is approximately half way between the geographic

ranges, as previously known, of _S. a. australis_ and _S. a. howelli_

(see Jackson, N. Amer. Fauna, 38, September 30, 1915).

The specimens recorded by Quay probably are two females in the

Cleveland Museum of Natural History bearing Catalogue Nos. 18136 and

18262 and labeled as from Springhill Plantation, Thomas County,

Georgia. We have examined these specimens and find that they resemble

_S. a. howelli_ in narrowness across the upper tooth-rows, but that

they resemble _S. a. australis_ in length of tail (22, 24), in

shortness of maxillary tooth-row (9.5, 9.5), and in convex dorsal

outline of the skull. Accordingly, we refer the specimens to _Scalopus

aquaticus australis_.

~Sorex cinereus cinereus~ Kerr

In his revision of the American long-tailed shrews, Jackson (N. Amer.

Fauna, 51, vi + 238, 13 pls., 24 figs., July 24, 1928) referred

specimens of _Sorex cinereus_ from Tyonek, Cook Inlet, Alaska, to the

subspecies _S. c. cinereus_ (_op. cit._: 46) and one specimen from

Chester Creek, Anchorage, Alaska, to the subspecies _S. c. hollisteri_

(_op. cit._: 56). Thus, the geographic ranges of the two subspecies

would seem to overlap around the northern shores of Cook Inlet. In an

attempt to resolve this seemingly anomalous distribution, we have

examined pertinent materials in the Biological Surveys Collection, U.S.

National Museum. We agree with Jackson (_op. cit._) that the series of

specimens from Tyonek is readily referable to _S. c. cinereus_. To our

eye, however, the specimen, No. 232691, from Anchorage is referable to

_Sorex cinereus cinereus_, rather than to _S. c. hollisteri_. The

reference is made on the basis of the darker color, especially of the

underparts. In this specimen, other characters that distinguish the two

mentioned subspecies are not apparent, probably because it is

relatively young; the teeth show only slight wear.

~Sorex trowbridgii humboldtensis~ Jackson

In his account of the long-tailed shrews, Jackson (N. Amer. Fauna,

51:98, July 24, 1928) listed under specimens examined of _Sorex

trowbridgii montereyensis_ four specimens from 7 mi. N Hardy, Mendocino

Co., California. Under his account of the subspecies _S. t. humboldtensis_,

however, he (_op. cit._:97) mentions that specimens (seemingly the same

four) from 7 mi. N Hardy "have shorter tails than typical representatives

of _humboldtensis_, but in color and cranial characters they are similar

to this [_humboltensis_] subspecies." We conclude, therefore, that the

specimens mentioned were inadvertently listed as _S. t. montereyensis_

and are _Sorex trowbridgii humboldtensis_. This conclusion is supported

by the fact that the locality concerned, 7 mi. N Hardy, is within the

geographic range assigned to _S. t. humboldtensis_ by Jackson (_op.

cit._:97); his southern records of occurrence of _S. t. humboldtensis_

are Sherwood and Mendocino, both in Mendocino County, California. Our

conclusion is further supported by Grinnell's (Univ. California Publ.

Zool., 40(2):80, September 26, 1933) statement of the range of _S. t.

montereyensis_ as "from southern Mendocino County south...."

~Blarina brevicauda churchi~ Bole and Moulthrop

Kellogg (Proc. U.S. Nat. Mus., 86:253, February 14, 1939) tentatively

referred specimens of the short-tailed shrew from the mountainous parts

of eastern Tennessee to the subspecies _Blarina brevicauda talpoides_,

with the remark that they were unlike specimens of that subspecies

obtained in eastern and southern West Virginia. Subsequently, Bole and

Moulthrop (Sci. Publ. Cleveland Mus. Nat. Hist., 5:109, September 11,

1942) named the subspecies _Blarina brevicauda churchi_ with type

locality at Roan Mountain, North Carolina. We have examined the

specimens in the U.S. National Museum recorded by Kellogg (_loc. cit._)

from the following localities: Shady Valley, 2900 ft. (Catalogue No.

267182); Holston Mtn., 4 mi. NE Shady Valley, 3800 ft. (Nos.

267176-267178, 267180, and 267181); Holston Mtn., 3 mi. NE Shady

Valley, 3000 ft. (No. 267179); Roan Mtn., (Nos. 267469-267475); Mt.

Guyot, 6300 ft. (No. 267183); 4-1/2 mi. SE Cosby, 3300 and 3400 ft.

(Nos. 267184 and 267185); and Snake Den Mtn., 3800 ft. (No. 267186).

Among named kinds of _Blarina brevicauda_, we find these specimens to

resemble most closely _Blarina brevicauda churchi_ and so refer them.

They are readily distinguishable from specimens of _B. b. kirtlandi_,

that occurs farther north in the same mountain range, by larger size

and longer tail. Incidentally, in the specimens that we have examined,

we do not find that _B. b. churchi_ is darker colored than other

subspecies of _Blarina brevicauda_; _B. b. churchi_, to us, is

indistinguishable in color from _B. b. kirtlandi_. Bole and Moulthrop

(_op. cit._) thought that _B. b. churchi_ was notably darker than other

subspecies from adjoining areas.

~Blarina brevicauda carolinensis~ (Bachman)

Blair (Amer. Midland Nat., 22(1):99, July, 1939) referred specimens of

the short-tailed shrew from the Arbuckle Mountain area of Oklahoma to

_Blarina brevicauda hulophaga_ and specimens from Mohawk Park, Tulsa

County, Oklahoma, to _B. b. carolinensis_. Later Bole and Moulthrop

(Sci. Publs. Cleveland Mus. Nat. Hist., 5:108, September 11, 1942) saw

two of the specimens from Mohawk Park and assigned them to _B. b.

hulophaga_. According to the most recent published account, therefore,

_B. b. hulophaga_ would seem to have a peculiarly discontinuous

geographic range. We have examined the material seen by Blair and by

Bole and Moulthrop (Nos. 75946, 75947, 75643, Mus. Zool. Univ.

Michigan) in an attempt to form our own judgment as to their

subspecific identity. The teeth of No. 75946 are well worn, whereas the

teeth of the other two are scarcely worn. We are unable to distinguish

No. 75946 from topotypes of _B. b. carolinensis_ by size, color, or

cranial features. The two younger specimens are smaller and paler, but

do not agree with the description of _B. b. hulophaga_. The

nearly-complete narrow, white girdle of No. 75947 is clearly an

individual variation. We assign the animals to _Blarina brevicauda

carolinensis_ (Bachman) as did Blair (_loc. cit._).

~Blarina brevicauda minima~ Lowery

Bailey (N. Amer. Fauna, 25:207, October 24, 1905) identified as

_Blarina brevicauda carolinensis_ one specimen from Joaquin and two

specimens from Big Thicket, 8 mi. NE Sour Lake, both localities in

eastern Texas. Strecker and Williams (Jour. Mamm., 10:259, August 10,

1929) later recorded the specimens again under the same name. The

subsequent naming of _B. b. plumbea_ from Aransas National Wildlife

Refuge, Aransas County, Texas (Davis, Jour. Mamm., 22(3):317, August

14, 1941) and _B. b. minima_ from Louisiana (Lowery, Occas. Papers Mus.

Zool., Louisiana St. Univ., 13:218, November 22, 1943) leaves the

identity of the specimens from eastern Texas in doubt. We have examined

the following specimens in the Biological Surveys Collection, U.S.

National Museum: No. 117372, from Joaquin; No. 136407, from 7 mi. NE

Sour Lake; and No. 136788, from 8 mi. NE Sour Lake. We judge these to

be the specimens referred to by Bailey (_loc. cit._). We find that they

are indistinguishable from specimens of _Blarina brevicauda minima_ and

they seem to differ from _B. b. plumbea_ in being chestnut rather than

plumbeous in color and in lacking the highly-arched posterior border of

the palate. They are easily distinguished from _B. b. carolinensis_ by

their chestnut, rather than slaty-black, color and small size. They are

distinguishable from _B. b. hulophaga_, to which they might conceivably

be referred on geographic grounds, by their color and small size. We

refer them to _Blarina brevicauda minima_ Lowery.

~Spilogale angustifrons angustifrons~ A. H. Howell

In his "Revision of the skunks of the genus Spilogale" (N. Amer. Fauna,

26, November 24, 1906) A. H. Howell identified certain specimens in the

United States National Museum as follows:

_Spilogale leucoparia_, [Male] sad. 55585 from Tulancingo, Hidalgo

(_op. cit._:21).

_Spilogale gracilis_, [Male] sad. 88154 from San Sebastian in

Jalisco, [Male] ad. 79017 from Lagos in Jalisco, [Male] ad. 47177

from Patzcuaro in Michoacan (_op. cit._:23).

_Spilogale ambigua_, [Male] ad. 35667/20437 from Barranca Ibarra in

Jalisco, [Male] yg. 120101 from Ocotlan in Jalisco (_op. cit._:25).

Hall and Villa (Univ. Kansas Publ., Mus. Nat. Hist, 1:448, December

27, 1949) inferred that No. 47177 from Patzcuaro was instead referable

to _Spilogale angustifrons angustifrons_. Our examination of No. 47177

and of each of the other specimens mentioned by catalogue number

immediately above leads us to conclude that they all are of one

species, and that, among named kinds of _Spilogale_, they should be

referred to the subspecies _Spilogale angustifrons angustifrons_

Howell.

Our examination of all of the specimens that Howell (_op. cit_.)

identified as _Spilogale [angustifrons] angustifrons_ reveals that

none of the specimens from the type locality had attained full adult

stature; the holotype is a subadult and the other specimens from the

type locality are even younger. The small size of these specimens from

the type locality seems to have misled Howell into thinking that they

were taxonomically distinct from the larger specimens--those from

Jalisco, Michoacan and Hidalgo--that he identified as other kinds.

~Spilogale gracilis gracilis~ Merriam

In the genus _Spilogale_ four specific names, concerning the status of

which we have been uncertain, are listed below in the order of their

appearance in the literature.

1890. _Spilogale gracilis_ Merriam, N. Amer. Fauna, 3:83,

September 11, type from bottom of canyon, Grand Canyon, Arizona.

1890. _Spilogale leucoparia_ Merriam, N. Amer. Fauna, 4:11,

October 8, type from Mason, Mason County, Texas.

1891. _Spilogale phenax arizonae_ Mearns, Bull. Amer. Mus. Nat.

Hist., 3:256, June 5, type from near Fort Verde, Yavapai County,

Arizona.

1897. _Spilogale ambigua_ Mearns, Preliminary diagnoses of new

mammals ... from the Mexican boundary line, p. 3, January 12

[reprinted in Proc. U.S. Nat. Mus., 20:460, December 24, 1897],

type from summit of Eagle Cliff Mtn., 2 mi. S of Monument No. 5 of

Emory's Survey which, according to Miller (U.S. Nat. Mus. Bull.,

128:134, April 29, 1924), is "Eagle Mountain, Chihuahua, Mexico,

about four miles south of Dona Ana County, New Mexico."

In 1906 (N. Amer. Fauna, 26:1-55, 10 pls., November 24) A. H. Howell's

"Revision of the skunks of the genus Spilogale" was published and the

four names listed above were retained by him as applying to four

species (not subspecies). His map (_op. cit._, pl. 1) showing the

geographic distribution of the four kinds looks reasonable enough at

first inspection and does not indicate any overlapping of the

geographic ranges of the species in question, but if a map be made by

plotting the localities of occurrence recorded by Howell (_op. cit._),

for specimens examined by him, a notably different geographic

distribution is shown. For one thing the geographic ranges of

_gracilis_, _leucoparia_, _arizonae_ and _ambigua_ coincide over a

considerable part of Arizona. Also, specimens collected in recent

years from Arizona and adjoining areas do not readily fit into the

"species" recognized by Howell; some specimens are structurally

intermediate between two or more of these species and other specimens

combine the diagnostic characters ascribed to two or more of the

alleged species. For these and other reasons a re-appraisal of the

application of the names mentioned above long has been indicated.

Before re-appraising the names it is pertinent to recall that Howell's

paper in 1906 on _Spilogale_ was only the second revisionary paper

that he prepared. It was prepared by a man who at that time lacked

much taxonomic experience, and who held to a morphotype concept.

Howell worked under the guidance, in the literal sense, of Dr. C. Hart

Merriam. The concept of species and subspecies held by Merriam

fortunately was recorded by him (Jour. Mamm., 1:6-9, November 28,

1919). Merriam's reliance on degree of difference and his disregard of

intergradation were naturally (and necessarily, we think, in Howell's

work in 1906) adopted by Howell. For example, of six specimens from

Point Reyes in west-central California, a place less than ten miles

from the type locality of _Spilogale phenax phenax_, Howell (_op.

cit._:33) assigned one specimen to the subspecies _Spilogale phenax

latifrons_! _S. p. latifrons_ occurs in Oregon and in northern

California--no nearer than 200 miles to Point Reyes. Howell's

assignment of this specimen to _S. p. latifrons_ was not a _lapsus_,

as persons with the modern (geographic) concept of a subspecies would

be likely to suppose. Howell's assignment of the one specimen to _S.

p. latifrons_ and the other five specimens to _S. p. phenax_ was

intentional, as he told one of us (Hall). He explained that he relied

upon the morphological characters of the individual animal instead of

upon the morphological characters of a population of animals. To him,

therefore, there was nothing inconsistent in his procedure in 1906.

Also, variation that was the result of difference in age and variation

that was the result of individual deviation were not understood, or at

least not taken into account, by Howell in 1906, nor by Merriam in

1890. For example, Merriam selected the most extensively white

specimen available to him for the holotype of _Spilogale leucoparia_.

He, and Howell in 1906, used the extensiveness of the white areas of

that particular specimen (see fig. 3, pl. 2, N. Amer. Fauna, 26, 1906)

as a character diagnostic of the "species" _S. leucoparia_ although

each of the authors had available two other specimens of _S.

leucoparia_ from the type locality, and all of the other referred

specimens in the United States National Museum, that were less

extensively white than the holotype. The _individual specimen_ was the

primary basis for the species or subspecies and one selected specimen

alone often was used in making comparisons between a given named kind

and some other species or subspecies. Also, be it remembered, degree

of difference, and not presence or absence of intergradation, was the

basis on which subspecific _versus_ specific rank was accorded to a

named kind of animal. Howell wrote on the labels of some specimens of

_Spilogale_ "not typical" when the individuals differed from the type

specimen in features that owe their existence to individual variation,

and he wrote the same words on the labels of other specimens that had

not yet developed mastoidal crests because the animals were not yet

adult.

Anyone who examines the specimens that Howell used will do well to

bear in mind the circumstances noted above concerning Howell's paper

of 1906; otherwise the reasons for Howell's identifications of certain

specimens can not be understood.

We have examined and compared the holotypes, and other specimens used

by Howell. While doing so we have borne in mind the degree of

individual variation well shown by each of several series of specimens

(for example, that in six adult males, from the Animas Mountains of

New Mexico, recorded by V. Bailey, N. Amer. Fauna, 53:339, 1932) and

age variation (for example, that shown in specimens of _S. interrupta_

from Douglas County, Kansas). The degree of each of these kinds of

variation, although considerable, is not extraordinary. That is to

say, the variations are of approximately the same degree as we

previously have ascertained to exist in _Mephitis mephitis_ and in

_Mustela frenata_, two species that are in the same family,

Mustelidae, as _Spilogale_. As a result of our comparisons, we

conclude, first that the four names mentioned at the beginning of this

account all pertain to one species, and second that the three names

_S. gracilis_, _S. p. arizonae_ and _S. ambigua_, and probably also

_S. leucoparia_, were based on individual variations in one

subspecies. _S. gracilis_ has priority and will apply; the other names

are properly to be arranged as synonyms of it, as follows:

1890. _Spilogale gracilis_ Merriam, N. Amer. Fauna, 3:83,

September 11.

1890. _Spilogale leucoparia_ Merriam, N. Amer. Fauna, 4:11,

October 8.

1891. _Spilogale phenax arizonae_ Mearns, Bull. Amer. Mus. Nat.

Hist., 3:256, June 5.

1897. _Spilogale ambigua_ Mearns, Preliminary diagnoses of new

mammals ... from the Mexican boundary line, p. 3, January 12.

Some information in support of the above arrangement, along with some

other observations on _Spilogale_, are as follows: The type specimen

of _Spilogale gracilis_ bears on the original skin-label in the

handwriting of Vernon Bailey, the collector, the statement that the

tail was imperfect. The recorded measurements of 400 for total length

and 142 for length of tail, therefore, are presumed to be subject to

correction. This presumption and the further circumstance that other

specimens from Arizona and New Mexico are as large as specimens of

comparable age and sex that we have examined from Nevada and Utah of

_Spilogale gracilis saxatilis_ Merriam, indicate that _S. g.

saxatilis_ differs less from the allegedly smaller _S. g. gracilis_

than was previously thought. Nevertheless, from north to south (for

example, from northern Nevada to southern Arizona) there is an

increase in extent of white areas at the expense of black areas of the

pelage. As a result, the lateralmost white stripe in _S. g. saxatilis_

averages narrower (and often is wanting) than in _S. g. gracilis_. The

absence, or narrowness, of the lateralmost white stripe seems to be

the principal basis for recognizing _S. g. saxatilis_, just as the

tendency to narrow rostrum in Coloradan specimens seems to be the

principal basis for recognizing _Spilogale gracilis tenuis_ A. H.

Howell. Both _S. g. saxatilis_ and _S. g. tenuis_ are "poorly"

differentiated from _S. g. gracilis_ and from each other.

The holotype of _Spilogale ambigua_ Mearns is slightly smaller than

other adult males of comparable age, and the braincase, relative to

its width, is slightly deeper than in the average adult male. These

variations, nevertheless, are within the range of individual

variation, as also are those characterizing the holotype of _Spilogale

phenax arizonae_ Mearns. The latter specimen is an adult male, with

much inflated mastoidal bullae, nearly straight dorsal profile on the

skull, relatively shallow braincase, and only slightly worn teeth.

The holotype of _Spilogale leucoparia_ Merriam, as pointed out above,

is an extreme example of the extensiveness of the white areas of the

pelage at the expense of the black areas. This feature occurs more

often in the southwestern desert areas of the United States than it

does farther north. In addition to the extensiveness of the white

markings, the other two characters allegedly distinctive of _S.

leucoparia_ are broad and much flattened braincase and great degree of

inflation of the mastoidal bullae. Although these three mentioned

features do distinguish _S. leucoparia_ from _S. indianola_ to the

eastward, they seem not to set _S. leucoparia_ apart from _S.

gracilis_ to the westward. For example, in Arizona some specimens are

extensively white and some others have the braincase flattened and the

mastoidal bullae much inflated. V. Bailey (N. Amer. Fauna, 53:339,

1932) refers to a specimen ([Male], No. 147252 USBS) from the head of

the Rio Mimbres in New Mexico in which, as our comparisons show, the

inflation of the mastoidal bullae exceeds that of any Texan specimen

of _S. leucoparia_, the holotype included. Also, at the type locality

of _S. leucoparia_, subadult male No. 188467 USNM and adult male No.

188468 USNM are narrower across the mastoidal region than is the

holotype. In summary and review, specimens from the eastern part of

the range heretofore ascribed to _S. leucoparia_ nearly all have much

inflated mastoidal bullae whereas less than half of the specimens of

_Spilogale_ from western New Mexico and Arizona have these bullae as

greatly inflated; but, in No. 147252 from the head of the Rio Mimbres

of New Mexico the inflation of the bullae is more extreme than in any

specimen that we know of that has been referred to _S. leucoparia_.

If intergradation occurs between _Spilogale gracilis gracilis_ and

_Spilogale indianola_ and between one or both of these kinds on the

one hand and _Spilogale interrupta_ on the other hand, central Texas

would be a logical place to collect intergrades. We suppose that such

intergradation will be found to occur and that eventually _Spilogale

putorius_ will be the specific name to apply to all of the Recent

subspecies of spotted skunks. Until proof of such intergradation is

forthcoming we employ current nomenclature.

~Spilogale gracilis microdon~ A. H. Howell

A. H. Howell (N. Amer. Fauna, 26:31, November 24, 1906) listed as

_Spilogale arizonae martirensis_ one specimen ([Female] sad.-yg.,

145886 USBS) from Comondu, which is the type locality of _S.

microdon_. Our examination of [Female] No. 145886 convinces us that it

is referable to _S. microdon_.

Examination of the materials used by Howell (_op. cit._) reveals that

there is an increase in size of animal and its skull from within the

geographic range of _S. g. martirensis_ southward to Cape St. Lucas

which is the type locality of _S. lucasana_. Specimens of _S.

microdon_, which so far has been recorded only from Comondu, the type

locality, are, as would be expected, intermediate in size between _S.

g. martirensis_ and _S. lucasana_. The differential characters of

these three named kinds of _Spilogale_ are principally those of size,

and we can see no characters judged to be of more than subspecific

worth. Consequently the named kinds should stand as:

_Spilogale gracilis martirensis_ Elliott;

_Spilogale gracilis microdon_ A. H. Howell;

_Spilogale gracilis lucasana_ Merriam.

~Spilogale gracilis microrhina~ Hall

When Hall (Jour. Mamm., 7:53, February 15, 1926) named as new

_Spilogale phenax microrhina_, he did not mention specimens previously

recorded by A. H. Howell (N. Amer. Fauna, 26:32, November 24, 1906) as

_Spilogale phenax_ from San Bernardino Peak (57026 USBS), La Puerta

(99580 USBS), Dulzura (55848, 56173, 56873, 33693/45728, 36291/48656

and 36292/48657) in southern California. On geographic grounds these

specimens would be expected to be _S. g. microrhina_ although

geographically slightly outside the area that could be delimited by

Hall's (_op. cit._) marginal record-stations of occurrence. Our

examination of the pertinent specimens reveals that they are

_Spilogale gracilis microrhina_. The localities from which the

specimens came are, respectively, the northeasternmost, easternmost

and southernmost occurrences so far listed for the subspecies.

~Conepatus mesoleucus mearnsi~ Merriam

Examination of the holotypes of _Conepatus filipensis_ Merriam,

_Conepatus pediculus_ Merriam, _Conepatus sonoriensis_ Merriam, and

_Conepatus mesoleucus mearnsi_ Merriam, and other specimens of the two

kinds last named, convinces us that all are the same species and that

the names should stand as follows: _Conepatus mesoleucus filipensis_

Merriam (type locality, Cerro San Felipe, Oaxaca); _Conepatus

mesoleucus pediculus_ Merriam (Sierra Guadalupe, Coahuila); and

_Conepatus mesoleucus sonoriensis_ Merriam (Camoa, Rio Mayo, Sonora).

One method of designating the ages of individuals in _Conepatus_ is

to recognize four categories from younger to older, as follows: 1)

juvenile--retaining one or more deciduous teeth; 2) young--sutures

open and clearly to be seen between bones of the facial part of the

skull; 3) subadult--skull of adult form, but lacking sagittal and

lambdoidal crests and retaining faint traces of sutures between facial

bones; and 4) adult--sutures obliterated, lambdoidal ridge high and

temporal ridges (of females) or sagittal crest (of males) prominent.

On this basis of designating age, the holotype of _C. pediculus_ is

young and nearer the juvenal than the subadult stage. Its small size

is partly the result of its youth. Other than its small size we find

no characters to distinguish it from _C. m. mearnsi_. Unfortunately no

young male of _C. m. mearnsi_ of the same age as the holotype of _C.

pediculus_ is available. Also, from the general area of the Sierra

Guadalupe, Coahuila, only the one specimen of _Conepatus mesoleucus_

(the holotype of _C. m. pediculus_) is known. Consequently, we can not

yet prove that some young males of _C. m. mearnsi_ are as small as the

holotype of _C. pediculus_. Because of this lack of proof we

tentatively recognize the subspecies _Conepatus mesoleucus pediculus_

instead of placing the name _Conepatus pediculus_ in the synonomy of

_Conepatus mesoleucus mearnsi_.

The holotype of _C. sonoriensis_ is a young female, older than the

holotype of _C. pediculus_, and approximately midway between the

juvenal and subadult stages.

The holotype of _C. filipensis_ is an adult male.

We suppose that _C. mesoleucus mesoleucus_ Lichtenstein and _C.

mesoleucus mearnsi_ Merriam on the one hand, and _Conepatus leuconotus

leuconotus_ Lichtenstein and _C. l. texensis_ Merriam on the other

hand will be found to intergrade, in which event the name _Conepatus

leuconotus_, having page priority over _Conepatus mesoleucus_, will

apply to the species. Proof of complete intergradation is not yet

available. The one difference between the two that prevents our

uniting them as subspecies of one species is the larger size of _C. l.

leuconotus_ and _C. l. texensis_. Measurements of the smallest adult

male and female available to us of _C. l. texensis_ and of the largest

adult male and female of _C. m. mearnsi_ are given below.

Where the geographic ranges of the two species approach one another

the only taxonomically significant difference detected by us is in

size, _C. leuconotus_ being larger than _C. mesoleucus_. Other

characters that are useful in separating the two alleged species now

are known to vary geographically in a fashion that indicates only

subspecific status for the two kinds. For example, three specimens

from Laredo, Texas (previously recorded by V. Bailey, N. Amer. Fauna,

25:205, October 24, 1905--Nos. 24839/32237, 24840/32238 and

24842/32245 USBS), bridge the gap in color pattern between _C. l.

texensis_ to the east and _C. m. mearnsi_ to the west. _C. l.

texensis_ characteristically has the white stripe terminating

anteriorly in an obtuse angle, and on the hinder back the area of

white is restricted to a narrow line or is wanting. _C. m. mearnsi_

characteristically has the white stripe truncate anteriorly and

approximately as broad on the hinder back as on the shoulders. In the

specimens from Laredo, the young female, No. 24842, has the white

nearly truncate anteriorly (pointed in the other two specimens, adult

females). In No. 24839 the area of white on the hinder back is only

slightly restricted in width (noticeably restricted but present in the

other two specimens).

The proof of intergradation, or the lack of it, between the two

alleged species, _Conepatus mearnsi_ and _Conepatus leuconotus_, would

seem to be profitably sought by obtaining specimens along the Rio

Grande in Texas between the Blocker Ranch ("50 miles southeast of

Eagle Pass") and Laredo.

Measurements illustrating the size difference between the two alleged

species are as follows:

Comments on the Taxonomy and Geographic Distribution of Some North American Marsupials, Insectivores and Carnivores · 第 5 / 6 题