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BULLETIN CARNEGIE MUSEUM OF NATURAL HISTORY NO. 32<br />
Fig. 11.-Ventral view of the skull of Crotaphytur dickrsonae<br />
(REE 2777, adult male. SVL = 116 mm). Scale = 5 mm.<br />
(Leiolepis belliana, Physignathus lesueurii). There-<br />
fore, the presence of a tubercle is considered to be<br />
the derived state and represents a synapomorphy<br />
for Crotaphytidae.<br />
There is also variation in the angle of the jugal<br />
where it serves as the ventrolateral border of the<br />
orbit. In Crotaphytus, the medial face of the jugal<br />
is oriented dorsolaterally at about a 45-degree angle<br />
over most of its length. In G. wislizenii, G. copei,<br />
and 15 of 3 1 G. silus, the medial face becomes pro-<br />
gressively more vertical anteriorly until it articulates<br />
with the palatine, lacrimal, and prefrontal. As a re-<br />
sult, the region of articulation of the three bones in<br />
Gambelia wislizenii, G. copei, and some G. silus is<br />
box-like because the jugal meets the palatine and<br />
prefrontal at perpendicular angles. In Crotaphytus<br />
and some G. silus, the jugal meets the prefrontal in<br />
a smooth, rounded arc. The box-like condition of<br />
the ventrolateral border of the orbit was approached<br />
only in Petrosaurus mearnsi. Uta stansburiana. Uma<br />
(but not Callisaurus, Cophosaurus, or Holbrookia<br />
rnaculata), one of two Enyalioides laticeps, and Lei-<br />
olepis belliana and is therefore considered to be the<br />
derived state within Crotaphytidae.<br />
PALATE<br />
Vorners (Character 16; Fig. 1 1, 12). -In Crota-<br />
phytus insularis and C. vestigium, a separate pair of<br />
small bones, here termed extravomerine bones, may<br />
be present posteromedially where the vomers and<br />
palatines meet (Fig. 12). These medially contacting<br />
bones appear to be the result of secondary ossifi-<br />
cation centers in the vomers. In many specimens,<br />
this additional bone is present on one side only and<br />
the region where the bone is absent is filled in by<br />
the vomer from that side. Extravomerine bones are<br />
present in all five C. insularis available for study,<br />
although it is found on the right side only in one<br />
specimen (REE 2797). It is also found on at least<br />
one side in ten of 27 C. vestigium. Extravomerine<br />
bones are not present in the outgroup taxa examined<br />
here and no evidence has been discovered docu-<br />
menting their presence in other lizard species.<br />
Therefore, the presence of either one or two extra-<br />
vomerine bones is considered to be the derived state.<br />
Palatines (Character 17; Fig. 6, 1 1, 12).-In Cro-<br />
raphytus, the dorsal surface of the maxillary process<br />
usually bears the palatine foramen (Fig. 6), which<br />
may be situated in the suture of the maxillary pro-<br />
cess and the prefrontal or completely within the<br />
palatine. In one C. collaris (USNM 2202 16), the<br />
foramina were located entirely within the palatine<br />
processes of the prefrontals. A well-developed,<br />
transversely oriented canal, associated with the in-<br />
termediate palatine branch of nerve VII (Oelrich,<br />
1956), projects medially from the palatine foramen<br />
(Fig. 6). In Gambelia, a palatine foramen is only<br />
rarely evident (five of 43 G. tvislizenii, zero of eight<br />
G. copei, two of 30 G. silus), although the canal, and<br />
presumably the intermediate palatine branch of<br />
nerve VII, are present. Instead of passing through<br />
the prefrontal and palatine bones, the tube passes<br />
through the connective tissue medial to the palatine<br />
process of the prefrontal along the lateral border of<br />
the orbitonasal fenestra. The absence of a palatine<br />
foramen in the great majority of Gambelia appears<br />
to be the result of the narrower palatine process of<br />
the prefrontal found in this taxon, rather than the<br />
absence or rerouting of the intermediate palatine<br />
branch of nerve VII. Some variation was observed