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cryptic species within the dendrophidion vinitor complex in middle ...

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SPECIES IN THE DENDROPHIDION VINITOR COMPLEX N Cadle 185<br />

some of <strong>the</strong> characters particularly useful<br />

for <strong>the</strong> three <strong>species</strong> covered <strong>in</strong> this paper.<br />

Dorsocaudal reductions were recorded as<br />

<strong>the</strong> subcaudal at which <strong>the</strong> reduction from<br />

eight to six dorsal scale rows on <strong>the</strong> tail<br />

occurred (Lieb, 1988). The po<strong>in</strong>t of posterior<br />

reduction of <strong>the</strong> dorsal scales was<br />

scored on each side of selected specimens<br />

as <strong>the</strong> ventral scute number at which <strong>the</strong><br />

reduction occurred and <strong>the</strong> dorsal rows<br />

<strong>in</strong>volved. For purposes of analyz<strong>in</strong>g <strong>in</strong>traspecific<br />

differences <strong>in</strong> mean snout–vent<br />

length (SVL) of adult males and females,<br />

specimens with SVL . 450 mm were<br />

considered adults (Goldberg, 2003; Stafford,<br />

2003). Similarly, because relative tail<br />

length <strong>in</strong>creases proportionally with SVL,<br />

<strong>the</strong> range of adult relative tail length (RTL)<br />

was assessed for <strong>in</strong>dividuals with SVL .<br />

300 mm because analyses showed that RTL<br />

approaches an asymptote at approximately<br />

this size. When measurements or meristic<br />

data for particular specimens are referred to<br />

<strong>in</strong> <strong>the</strong> text, <strong>the</strong>se data are based on my<br />

exam<strong>in</strong>ations (data encountered <strong>in</strong> <strong>the</strong><br />

literature sometimes differ).<br />

Intraspecific mean differences between<br />

male and female sizes and scale counts were<br />

tested for significance us<strong>in</strong>g t tests after<br />

test<strong>in</strong>g for homogeneity of variances. P-<br />

values reported for <strong>in</strong>traspecific comparisons<br />

are two-tailed pairwise comparisons; <strong>in</strong><br />

<strong>the</strong> few cases <strong>in</strong> which <strong>the</strong>re was a priori<br />

expectation for one sex or <strong>the</strong> o<strong>the</strong>r to have<br />

a greater value for a character (e.g., males<br />

hav<strong>in</strong>g a longer tail or more subcaudals than<br />

females), p-values for one-tailed tests did<br />

not differ from <strong>the</strong> two-tailed comparison.<br />

Similar procedures and two-tailed tests<br />

were used for <strong>in</strong>terspecific comparisons,<br />

which were analyzed separately for each sex<br />

except <strong>in</strong> cases <strong>in</strong> which <strong>in</strong>traspecific sexual<br />

differences were nonsignificant (sexes<br />

pooled <strong>in</strong> <strong>the</strong>se cases). Means, standard<br />

deviations, and results of <strong>in</strong>traspecific statistical<br />

comparisons for most meristic counts<br />

are presented <strong>in</strong> Table 1, and only summaries<br />

are given <strong>in</strong> <strong>the</strong> text.<br />

For determ<strong>in</strong><strong>in</strong>g tail breakage frequencies,<br />

I counted as ‘‘broken’’ only tails with a<br />

clearly healed cap on <strong>the</strong> stump; thus, I<br />

record <strong>the</strong> frequency of ‘‘broken/healed’’<br />

tails. In my survey of literature, it was<br />

apparent that some authors <strong>in</strong>cluded any<br />

specimens with a tail fracture <strong>in</strong> <strong>the</strong>ir tail<br />

breakage frequency calculations (e.g., at<br />

least one paper recorded multiple fracture<br />

po<strong>in</strong>ts <strong>in</strong> a high percentage of specimens).<br />

However, this method artificially <strong>in</strong>flates<br />

estimates of tail breakage frequencies because<br />

of <strong>the</strong> <strong>in</strong>clusion of snakes whose tails<br />

were broken dur<strong>in</strong>g or after capture, or<br />

even subsequent to storage <strong>in</strong> a museum jar.<br />

Although <strong>the</strong>se specimens may offer clues<br />

as to <strong>the</strong> fragility of <strong>the</strong> tail <strong>in</strong> a particular<br />

<strong>species</strong>, <strong>the</strong>y are not especially useful for<br />

comparative purposes.<br />

I scored <strong>the</strong> number of keeled dorsal<br />

scale rows on <strong>the</strong> neck, at midbody, and just<br />

anterior to <strong>the</strong> vent. Keels <strong>in</strong> all <strong>species</strong> of<br />

Dendrophidion are best developed (i.e.,<br />

encompass<strong>in</strong>g more dorsal rows) on <strong>the</strong><br />

posterior body, but <strong>the</strong> number of keeled<br />

rows on <strong>the</strong> neck or at midbody often show<br />

<strong>in</strong>terspecific differences that provide discrim<strong>in</strong>at<strong>in</strong>g<br />

characters. The three <strong>species</strong><br />

covered <strong>in</strong> this paper are similar <strong>in</strong> <strong>the</strong>ir<br />

patterns of keel<strong>in</strong>g. The basic pattern of<br />

temporal scales <strong>in</strong> D. <strong>v<strong>in</strong>itor</strong> and <strong>the</strong> new<br />

<strong>species</strong> here described is 2+2 (two primary,<br />

two secondary). However, temporal scales<br />

were often divided by a vertical suture<br />

(usually divid<strong>in</strong>g <strong>the</strong> scale asymmetrically),<br />

or, less commonly, two temporal scales were<br />

fused or a temporal was fused with a<br />

supralabial. I recorded <strong>the</strong>se divisions or<br />

fusions separately from <strong>the</strong> basic pattern.<br />

For example, a specimen might be recorded<br />

as hav<strong>in</strong>g 2+2 temporals but with <strong>the</strong> upper<br />

primary and upper secondary fused on one<br />

side. Because of frequent asymmetry, temporal<br />

scales and supra- and <strong>in</strong>fralabials were<br />

scored on each side of a specimen, and each<br />

side was treated as an <strong>in</strong>dependent observation;<br />

<strong>the</strong> total count of observations for<br />

<strong>the</strong>se scale characters (Table 1) is thus<br />

about twice <strong>the</strong> number of specimens<br />

exam<strong>in</strong>ed (damage sometimes prevented<br />

scor<strong>in</strong>g on one or both sides of a given<br />

specimen).<br />

Bullet<strong>in</strong> of <strong>the</strong> Museum of Comparative Zoology harv-160-04-01.3d 11/4/12 19:58:33 185

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