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1996 McGUIRE- SYSTEMATICS OF CROTAPHY TID LIZARDS 57<br />
just reaches forelimb insertion, (2) terminates (I) golden tan; (2) straw yellow; (3) aquamarine<br />
within antehumeral fold, (3) terminates before to cobalt blue; (4) brown; (5) olive green, turentering<br />
antehumeral fold.<br />
76. Dark nuchal spots (P): (0) absent, (I) present.<br />
quoise, or gray.<br />
77. Inguinal patches (P): (0) absent, (I) present.<br />
78. Inguinal patches (U): (0) small, (1) large (taxa<br />
without inguinal patches coded as unknown<br />
["?"I)<br />
79. Femoral pore secretions (P): (0) off-white to gray,<br />
(1) black.<br />
80. Black pigmentation in central region of gular<br />
BEHAVIOR<br />
86. Saxicoly (including the use of saltatory bipedal<br />
locomotion in rocky habitats) (U): (0) absent,<br />
(1) present.<br />
87. Territoriality (P): (0) present, (1) absent.<br />
88. Lateral tail coiling (P): (0) absent, (1) present.<br />
pattern (U): (0) absent, (1) present.<br />
8 1. Peripheral gular pattern (U): (0) reticulated, (1)<br />
pale spots or radiating oblique stripes.<br />
82. Gular pattern (U): (0) present only in adults and<br />
well developed in males only, (1) well developed<br />
in all age classes and in both sexes.<br />
83. Enlarged melanic axillary patches (P): (0) absent,<br />
(1) present.<br />
84. Ventrolateral coloration (P, UO): (0) does not<br />
differ from ventral coloration (white), (1) olive<br />
green, (2) orange, (3) blue.<br />
85. Dorsal coloration (U, UO): (0) off-white to tan;<br />
ALLozYMES<br />
89. H-LDH (U): four electromorphs.<br />
90. aGPD (U): two electromorphs.<br />
9 1. 6-PGD (U): three electromorphs.<br />
92. ICDs (U): four electromorphs.<br />
93. ICDm (U): four electromorphs.<br />
94. GOTs (U): three electromorphs.<br />
95. Pro (U): two electromorphs.<br />
96. Est 1 (U): three electromorphs.<br />
97. Hbpf (U): two electromorphs.<br />
98. Tr (U): four electromorphs.<br />
An initial analysis was performed on the mor-<br />
phological data set of 88 characters (allozyme data<br />
of Montanucci et al. [I9751 not included). This re-<br />
sulted in the discovery of a single tree (Fig. 37) with<br />
a length of 12,334 (123.34 when the effect of weight-<br />
ing the characters is removed) and a consistency<br />
index (CI; excluding uninformative characters) of<br />
0.761, a retention index (RI) of 0.848, and a g, tree<br />
length frequency distribution skewness value of<br />
- 1.49 (the critical g, value for this data set when<br />
randomized is -0.16 [P 5 0.01 1); Table 1). This CI<br />
is greater than that expected for an analysis of 13<br />
taxa (expected CI = 0.649; Sanderson and Dono-<br />
ghue, 1989), indicating that there is less homoplasy<br />
than expected in these data when compared with<br />
the 60 data sets reexamined by Sanderson and Don-<br />
oghue (1989). The g, value is strongly left skewed<br />
suggesting that the data are phylogenetically infor-<br />
mative. The tree generated in the bootstrap analysis<br />
is presented in Figure 38.<br />
Reanalysis of the allozyme data set of Montanucci<br />
et al. (1 975) using the Manhattan distance frequency<br />
approach resulted in the discovery of a single most<br />
parsimonious tree (Fig. 39A). The tree length fre-<br />
quency distribution data, summarized by the g, sta-<br />
RESULTS<br />
tistic (Hillis and Huelsenbeck, 1992), suggests that<br />
there is phylogenetically informative signal in this<br />
data set (observed g, value of -0.50; the critical g,<br />
value for this data set when randomized is -0.45<br />
[P r 0.011). The bootstrap tree for the analysis is<br />
given in Figure 39B (see comments below regarding<br />
interpretation of bootstrap P values).<br />
Because analysis of both the morphological and<br />
allozyme data sets suggests that they contain phy-<br />
logenetic signal, these data sets were combined and<br />
the larger data set was analyzed. Analysis of the<br />
combined morphology and allozyme data sets re-<br />
sulted in the same tree as did the analysis of the<br />
morphology data alone (Fig. 37). The tree length is<br />
139.91, while the C1 (excluding uninformative char-<br />
acters) for the combined tree is 0.761, the RI is<br />
0.848, and the g, value is - 1.45 (critical g, value<br />
= -0.15 [P I 0.0 I]). PAUP is unable to incorporate<br />
the step matrix characters into the CI and RI cal-<br />
culations, which explains why the CI and RI values<br />
are identical to those discovered in the analysis of<br />
the morphological data alone. The g, and CI values<br />
indicate that the data harbor substantial phyloge-<br />
netic signal. The 50 percent majority-rule consensus<br />
tree generated in the bootstrap analysis of the com-