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102 BULLETIN CARNEGIE MUSEUM OF NATURAL HISTORY NO. 32<br />
Il1usrrations.-Black-and-white photographs of<br />
adult lizards were provided in Banta and Tanner<br />
( 1968) and Montanucci (1 978).<br />
Taxonotnic Remarks.-Gambelia copei and G.<br />
wislizenii are easily distinguished on the basis of<br />
their coloration (see diagnosis above). However,<br />
geographic variation in the dorsal coloration of<br />
Gambelia wislizenii is extensive and this alone is<br />
not particularly compelling evidence for the recog-<br />
nition of copei as a distinct species. The primary<br />
motivation for this taxonomic rearrangement is the<br />
occurrence of both forms in syntopy along a narrow<br />
zone within Paseo de San Matias in northeastern<br />
Baja California. Within Paseo de San Matias, in-<br />
dividuals that are easily identified to species occur<br />
together in the same microhabitat over a zone of<br />
1.6 km without showing any obvious evidence of<br />
intergradation. Aside from this narrow contact zone,<br />
the distributions of G. copei and G. tvislizenii are<br />
widely separated.<br />
Paseo de San Matias is a low elevation dispersal<br />
corridor that connects the lower Colorado Desert<br />
with the coastal region of northwestern Baja Cali-<br />
fornia. Several desert species extend their ranges<br />
westward toward the Pacific coast by way of this<br />
corridor and some coastal species nearly reach the<br />
desert by extending eastward (Welsh and Bury,<br />
1984). It may appear as though G. copei and G.<br />
tvislizenii are geographic variants and that the pat-<br />
tern change is the result of in situ selection where<br />
the habitat changes from extremely xeric creosote<br />
desert to more mesic mountainous terrain. How-<br />
ever, typical G. copei occur in the lower Colorado<br />
Desert region in the vicinity of Bahia de San Luis<br />
Gonzaga, documenting that the distinctive color<br />
pattern of G. copei is not another G. rvislizenii pat-<br />
tern type that appears only in mesic habitats. Gam-<br />
belia copei in the Bahia de San Luis Gonzaga region<br />
are approached by G. wislizenii in the vicinity of<br />
Puertocitos, where they are separated by a trans-<br />
verse volcanic field that is 31.5 road km in width.<br />
This lava field extends from the peninsular ranges<br />
to the edge of the Gulf of California and appears to<br />
be a dispersal bamer for Gantbelia. Because the<br />
color pattern differences noted above are main-<br />
tained in these populations, which occur in essen-<br />
tially identical habitats that are separated only by<br />
the lava field, the notion that the G. copei and G.<br />
wislizenii color pattern differences are the result of<br />
in situ selection is unlikely. Nevertheless, because<br />
this taxonomic decision is based only on differences<br />
in coloration that are relatively subtle, on a single<br />
osteological character that differs in frequency (the<br />
presence of a well-developed tubercle on the an-<br />
terolateral margin of the postorbital was present in<br />
all G. copei examined [n = 81, whereas in G. wisli-<br />
zenii, the tubercle usually is absent [present in four<br />
of 49 specimens]), and on presumed reproductive<br />
isolation in this region, the recognition of G. copei<br />
as a full species is considered tentative. Electropho-<br />
retic analyses of the Paseo de San Matias popula-<br />
tions are planned in order to determine if fixed al-<br />
lelic differences can be detected that are consistent<br />
with the dorsal color pattern data.<br />
Montanucci (1978) considered the populations of<br />
Gantbelia on Isla Tiburon and coastal Sonora be-<br />
tween Puerto Libertad and Bahia Kino to be<br />
con(sub)speci fic with copei. Although there are no-<br />
table similarities between certain individuals from<br />
the coastal Sonoran region and those from Baja Cal-<br />
ifornia (particularly in CAS 17050 from the south-<br />
eastern end of Isla Tiburon), they differ in that the<br />
Sonoran lizards have spots that continue onto the<br />
dorsal surface of the head, whereas G. copei nearly<br />
always lack this spotting. While some individuals<br />
from coastal Sonora clearly resemble those of Baja<br />
California, the majority examined here were char-<br />
acteristic of those of the remaining portions of So-<br />
nora.<br />
Gantbelia coronat Norell<br />
Gantbelia corona Norell, 1989:ll; fig. 10. Type locality: LACM<br />
locality 7058, Vallecito Badlands, Anza-Borrego Desert State<br />
Park (holotype: LACM 42880).<br />
Er)~mology.-From the Latin corona, a crown, in reference to<br />
the distinctive characteristics of the frontal and irontoparietal<br />
suture.<br />
Diagnosis. - Gambelia coronat is distinguished<br />
from other Gambelia by the presence of the fron-<br />
toparietal suture anterior to the posterior extent of<br />
the orbits. It is further distinguished from Gambelia<br />
copei and G. tvislizenii by the presence of a trans-<br />
versely concave frontal bone.<br />
Distribution. -Known only from the type locality.<br />
Rentarks. -Gambelia coronat is an extinct spe-<br />
cies known only from a fossilized skull and man-<br />
dibles. Black-and-white photographs of dorsal and<br />
lateral views of the skull were provided by Norell<br />
(1 989).<br />
Gambelia silus Stejneger<br />
Croraphytus silus Stejneger, 1890: 105. Typ locality: "Fresno,<br />
Cal." (holotype: USNM 1 1790A).<br />
Cruraphytus ~vislizenii-Cope, 1 900:255.