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McGUIRE-SYSTEMATICS OF CROTAPHYTID LIZARDS<br />

Gypsum Cave, Clark County. Nevada (Brattstrom,<br />

1954), and Smith Creek Cave, White Pine County,<br />

Nevada (Mead et al., 1982) were identified as Cro-<br />

taphytus collaris. All fall within the current distri-<br />

butional range of C. bicinctores and therefore, on<br />

distributional grounds, may be more appropriately<br />

referred to this taxon.<br />

Natural History.-Many anecdotal reports re-<br />

garding the natural history of Croraphytus bicinc-<br />

(ores have appeared, although no general treatment<br />

of the ecology of the species has been published.<br />

The species occurs in some of the most inhospitable<br />

regions of North America including the rugged, vol-<br />

canic basin and range mountains of the Sonoran,<br />

Mojave, and Great Basin deserts. It is generally re-<br />

stricted to rocky habitats with scant vegetation, such<br />

as alluvia, lava flows, mountain sides, canyons, and<br />

rocky plains, but occasionally may be found in pe-<br />

ripheral areas with only limited rocky cover. I have<br />

observed individuals more than a mile away from<br />

the nearest extensive rocky habitat in association<br />

with rolling gravely hills with only occasional rocks.<br />

Their ability to inhabit such areas may allow this<br />

species to disperse across the suboptimal habitats<br />

that separate isolated desert mountain ranges, as<br />

they are known to inhabit numerous isolated moun-<br />

tain systems. These are diurnal lizards often seen<br />

perched atop dark volcanic rocks at temperatures<br />

over 37°C. When disturbed, they may take refuge<br />

beneath a nearby stone or bound bipedally from one<br />

rock to the next before taking refuge under a stone<br />

or in a nearby rodent hole. Although primarily sax-<br />

icolous, this species occasionally may ascend small<br />

shrubs (Banta, 1967). possibly to avoid high sub-<br />

strate temperatures or in search of food.<br />

The diet of this species appears to consist pri-<br />

marily of arthropods, including orthopterans, co-<br />

leopterans, hemipterans, homopterans, hymenop-<br />

terans, lepidopterans, and arachnids, as well as small<br />

vertebrates (Camp, 19 16; Knowlton and Thomas,<br />

1936; Snyder, 1972; Nussbaum et al., 1983; per-<br />

sonal observation). Uta stansburiana is probably the<br />

most commonly consumed vertebrate species (Sny-<br />

der, 1972; personal observation), although other re-<br />

corded taxa include Sceloporus. Cnernidophorus,<br />

Phrynosoma, and Xantusia vigilis (Banta, 1960;<br />

Nussbaum et al., 1983). As do other crotaphytids,<br />

C. bicinctores occasionally includes plant matter in<br />

its diet (Banta, 1960).<br />

Snyder (1972) found that adult Crotaphytus bi-<br />

cinctores in northwestern Nevada may become ac-<br />

tive as early as April 17 and large numbers may be<br />

observed in early May. I have observed adults active<br />

as early as March 19 in southwestern Arizona. In<br />

southeastern California, I have observed juveniles<br />

(probably hatched the previous season), gravid fe-<br />

males, and adult males on May 2, indicating that<br />

mating activities probably commenced in April. Ne-<br />

onates have been observed in August in eastern Or-<br />

egon (Brooking, 1934). Axtell (1972) hatched eggs<br />

in the laboratory on September 19. Andre and<br />

MacMahon (1 980) studied the reproductive biology<br />

of C. bicinclores in Tule Valley, Millard County,<br />

Utah. They discovered that females reached repro-<br />

ductive maturity at 85 mm SVL. All females sur-<br />

veyed in the first week of June contained oviducal<br />

eggs and by the end of June no females contained<br />

yolked follicles or oviducal eggs. Mean clutch size<br />

was reported as 5.38 with a range of three to seven.<br />

Larger females were found to produce larger clutches<br />

of eggs.<br />

Moehn (1976) showed that exposure to sunlight<br />

stimulates aggressive activity and despotism in cap-<br />

tives of this species. Sanborn and Loomis (1979)<br />

discussed male display patterns. Smith (1 974) noted<br />

that C. bicinctores may elicit a high-pitched squeal<br />

when under duress. Snyder (1972) discussed home<br />

range size and territoriality in populations adjacent<br />

to Pyramid Lake, Storey County, Nevada.<br />

Illustrarions.-A detailed black-and-white illus-<br />

tration ofthe entire animal was provided in Stebbins<br />

(1954); line drawings of the head squamation were<br />

included in Bun (1 928b:fig. 8) and Axtell (1972).<br />

Line drawings of the dorsal and ventral color pat-<br />

terns were given in Smith and Tanner (1 974); black-<br />

and-white photographs were provided in Axtell<br />

(1972). Pickwell (1 972), Smith and Tanner (1 972),<br />

and Nussbaum et al. (1983); color photographs were<br />

given by Behler and King (1979) and Sprackland<br />

(1990, 1993).<br />

Croraphyius collaris Say<br />

Agama collaris Say, 1823:252. Type locality: not given; Arkansas<br />

Tenitory (now Oklahoma) near the Verdigris River implied<br />

(holotype: Academy of Natural Sciences of Philadelphia, now<br />

lost). Restricted type locality (Stejneger, 1890): "the Verdigris<br />

River. near its junction with the Neosho River, Creek Nation,<br />

Indian Temtory"; (Stejneger and Barbour. 19 17): "Verdigris<br />

River near its union with the Arkansas River, Oklahoma";<br />

(Webb, 1970): "near Colonel Hugh Glenn's Trading Post on<br />

the east bank of the Verdigris River, about two miles above<br />

its confluence with the Arkansas River"; (Axtell. 1989~): Verdigris<br />

River near its union with the Arkansas River. Oklahoma.<br />

Croraphyrus collaris- Holbrook, 1842:79; pl. 10.<br />

Leiosaurus collaris-Dumkril, 1856:532.<br />

Croraphyrus baileyi Stejneger (syn. fide Cope, 1900), 1890: 103;<br />

fig. 1.2. Type locality: "Painted Desert, Little Colorado River,<br />

Arizona" (holotyp: USNM 1582 1).

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