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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

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