SPHENOPHRYNE - American Museum of Natural History
SPHENOPHRYNE - American Museum of Natural History
SPHENOPHRYNE - American Museum of Natural History
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2000 ZWEIFEL: PARTITION OF <strong>SPHENOPHRYNE</strong><br />
109<br />
Fig. 66. Dorsal (upper) and ventral views <strong>of</strong><br />
skull <strong>of</strong> Sphenophryne cornuta, AMNH A92804;<br />
scale bar measures 5 mm.<br />
<strong>of</strong> Liophryne allisoni (fig. 70). Although ventromedial<br />
thickening <strong>of</strong> the hyoid and the<br />
protruding process evidently are not pertinent<br />
at the level <strong>of</strong> specific and generic inquiry<br />
here, this morphology may prove to be an<br />
apomorphic state for the Microhylidae.<br />
APPENDAGES<br />
TERMINAL PHALANGES: The tips <strong>of</strong> the<br />
bones may bear T-shaped expansions whose<br />
span is more than twice the width <strong>of</strong> the base<br />
<strong>of</strong> the bone, or at the other extreme the tip<br />
may be bluntly rounded with only a slight<br />
subterminal constriction, its width less than<br />
that <strong>of</strong> the base. The relative breadths <strong>of</strong> the<br />
fleshy terminal disc and that <strong>of</strong> the phalangeal<br />
‘‘T’’ are closely correlated. The terminal<br />
discs are discussed further under Body Form<br />
and Proportions. The terminal phalanx <strong>of</strong> the<br />
third finger, which generally shows the greatest<br />
expansion <strong>of</strong> any <strong>of</strong> the hand’s digits, illustrates<br />
the range <strong>of</strong> variation (fig. 71).<br />
Among specimens <strong>of</strong> 20 species (one examined<br />
by dissection), the span <strong>of</strong> the tip relative<br />
to the length <strong>of</strong> the phalanx or to the<br />
width <strong>of</strong> its base falls into one <strong>of</strong> three discrete<br />
groups: (1) tip span/length <strong>of</strong> 0.24 and<br />
0.32 in Oxydactyla alpestris and O. stenodactyla<br />
(species with narrow, discless fingers);<br />
(2) <strong>of</strong> 0.54–0.82 in 13 species known<br />
or suspected to be litter-dwelling or surface<br />
active species; and (3) <strong>of</strong> 1.09–1.36 in five<br />
species <strong>of</strong> scansorial (Sphenophryne cornuta),<br />
riparian (Austrochaperina palmipes, A.<br />
rivularis, A. derongo, and A. basipalmata)<br />
habits.<br />
AXIAL SKELETON<br />
PRESACRAL VERTEBRAE: There are invariably<br />
eight nonimbricate presacrals, as described<br />
for the Australian species (Zweifel,<br />
1985b: 355). Variations in the transverse processes<br />
include relative lengths and angular<br />
orientation among vertebrae. For example, I<br />
find relatively long processes on vertebrae 2–<br />
4 and a strong anterior orientation to those<br />
on vertebrae 7 and 8 in Austrochaperina derongo,<br />
A. rivularis, A. pluvialis, and A. palmipes,<br />
whereas in Oxydactyla stenodactyla<br />
the processes are more similar in length and<br />
more nearly at a right angle to the column.<br />
Morphologies <strong>of</strong> the other species do not indicate<br />
that a classification <strong>of</strong> discrete types is<br />
possible.<br />
SACRAL VERTEBRAE: The sacral vertebrae<br />
are slightly to moderately expanded in most<br />
species discussed here, more so in one or two<br />
(figs. 72, 73). As an index <strong>of</strong> expansion I use<br />
the ratio <strong>of</strong> broadest diapophyseal measurement<br />
(anterior–posterior) to the span between<br />
ends <strong>of</strong> left and right diapophyses, excluding<br />
terminal cartilaginous extensions; a larger<br />
number implies broader diapophyses.<br />
Among 37 specimens <strong>of</strong> 19 species, including<br />
three Australian endemics, this ratio