SPHENOPHRYNE - American Museum of Natural History
SPHENOPHRYNE - American Museum of Natural History
SPHENOPHRYNE - American Museum of Natural History
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46 BULLETIN AMERICAN MUSEUM OF NATURAL HISTORY NO. 253<br />
one-half length <strong>of</strong> second, all with somewhat<br />
pointed, grooved terminal discs slightly<br />
broader than the terminal phalanges, subarticular<br />
and metacarpal elevations barely indicated<br />
(fig. 57B). Toes unwebbed, relative<br />
lengths 4 3 5 2 1, discs larger than<br />
those on fingers, slightly pointed and<br />
grooved, subarticular elevations barely evident,<br />
a small inner but no outer metatarsal<br />
elevation (fig. 57B). A brief, weak postocular<br />
fold; other dorsal and ventral body surfaces<br />
smooth.<br />
A color transparency furnished by Harold<br />
Cogger shows a frog with a dark, almost<br />
black ground color, an abundance <strong>of</strong> small<br />
white spots, and between these are numerous<br />
smaller, brick-red spots.<br />
The dorsal ground color in preservative is<br />
tan with no regional differentiation except<br />
that the loreal region is slightly duskier. A<br />
pattern <strong>of</strong> tiny pale spots on all the dorsal<br />
surfaces, including the legs, is uniform except<br />
for greater density on the eyelids. The<br />
ventral surfaces are slightly paler with a uniform<br />
pattern <strong>of</strong> pale spots larger and sparser<br />
than those <strong>of</strong> the dorsum.<br />
VARIATION IN TYPE SERIES: Variation in<br />
proportions is set forth in table 2, and regression<br />
data are in table 3. The largest <strong>of</strong><br />
61 specimens I measured is a female, SVL<br />
21.9 mm. Females as small as 18.2 mm are<br />
gravid, whereas one at 17.1 mm appears just<br />
to be maturing. The largest male measured<br />
19.0 mm. Tyler (1967) reported adult males<br />
15.5–17.2 mm SVL and adult females 17.0–<br />
20.1 mm SVL.<br />
There is little variation in color pattern.<br />
The dorsal ground color <strong>of</strong> preserved specimens<br />
may range from light to dark brown<br />
with the top <strong>of</strong> the snout and loreal region<br />
even darker, and the light spots may be less<br />
abundant medially on the back, snout and<br />
eyelids.<br />
ILLUSTRATIONS: 3rd finger terminal phalanx,<br />
fig. 71K; premaxilla, fig. 64B; vomer,<br />
fig. 65J; hand and foot, fig. 57B.<br />
CALL: The call has not been described.<br />
COMPARISONS WITH OTHER SPECIES: Tyler<br />
(1967: 188) characterized the coloration <strong>of</strong><br />
specimens from Keravat as agreeing ‘‘in all<br />
respects with that <strong>of</strong> the holotype’’ <strong>of</strong> Sphenophryne<br />
mehelyi, which Parker (1934: 156)<br />
described as ‘‘uniformly brown above, the<br />
flanks with scattered lighter dots; lower surfaces<br />
dirty white, the throat and chest washed<br />
with pale brown and irregularly spotted with<br />
white.’’ Méhely¨’s (1901: pl. 12, fig. 3) illustration<br />
<strong>of</strong> the ventral surface <strong>of</strong> mehelyi (as<br />
Chaperina fusca) agrees with Parker’s description<br />
rather than with the light brown,<br />
white spotted chin, chest, and abdomen <strong>of</strong><br />
novaebritanniae. For additional comparison<br />
with mehelyi, see the account <strong>of</strong> that species.<br />
A. novaebritanniae and the similar yelaensis<br />
are compared the account <strong>of</strong> the latter.<br />
HABITAT AND HABITS: Tyler (1967) described<br />
the Keravat locality as one that three<br />
months prior to the collection <strong>of</strong> the frogs<br />
had been cleared <strong>of</strong> virgin rainforest. Large<br />
numbers <strong>of</strong> frogs were aggregated beneath<br />
piles <strong>of</strong> decomposing vegetation—rotting<br />
grass and reeds laid upon ground covered<br />
with leaf mould. Numerous frogs were in<br />
small depressions, sitting on clumps <strong>of</strong> five<br />
or six eggs. The frogs in attendance were<br />
said to be females, although it is not clear<br />
whether the collector segregated the associated<br />
individual specimens with their egg<br />
clutches or if sex was merely assumed.<br />
DISTRIBUTION: The only known localities<br />
for this species (see Holotype and Paratypes,<br />
above) are at the northern end <strong>of</strong> New Britain<br />
(fig. 30).<br />
Austrochaperina palmipes (Zweifel),<br />
new combination<br />
Figure 31F<br />
Sphenophryne palmipes Zweifel, 1956: 15 (type<br />
locality, ‘‘north slope <strong>of</strong> Mt. Dayman, Maneau<br />
Range, Territory <strong>of</strong> Papua [Milne Bay Province,<br />
Papua New Guinea], at an elevation <strong>of</strong> 700 meters’’;<br />
holotype AMNH A57331, collected by<br />
G. M. Tate on the Fourth Archbold Expedition<br />
to New Guinea, July 16, 1953.<br />
DIAGNOSIS: This species differs from other<br />
Austrochaperina in its extensively webbed<br />
toes and usually in having a prominent,<br />
downward-directed, spikelike projection on<br />
each vomer.<br />
MORPHOLOGY: The holotype, an adult male<br />
36.1 mm SVL, is described in detail in Zweifel<br />
(1956: 15–17). Size moderately large<br />
among Austrochaperina, maximum about 40<br />
to 49 mm SVL, evidently varying among<br />
populations (see Variation, below), with