Litoria pinocchio, Oliver & Günther & Richards, 2019

Oliver, Paul M., Günther, Rainer & Richards, Stephen J., 2019, Systematics of New Guinea treefrogs (Litoria: Pelodryadidae) with erectile rostral spikes: an extended description of Litoria pronimia and a new species from the Foja Mountains, Zootaxa 4604 (2), pp. 335-348 : 341-345

publication ID

https://doi.org/10.11646/zootaxa.4604.2.6

publication LSID

lsid:zoobank.org:pub:150B04BB-EE8B-4FC5-A908-462FEFCD0530

persistent identifier

https://treatment.plazi.org/id/3F3E87D4-FFFC-6618-35FF-A708AAEE72A3

treatment provided by

Plazi

scientific name

Litoria pinocchio
status

sp. nov.

Litoria pinocchio sp. nov.

Northern Pinocchio Treefrog

Figs. 4–5 View FIGURE 4 View FIGURE 5 .

Holotype. MZB amph 15094 (F-num SJR 13612 View Materials ), adult male with tissue preserved in ethanol, Foja Mountains (2.590° S, 138.720° E), Papua Province, Indonesia, at approximately 1250 m a.s.l, collected by Paul Oliver on 21 November 2008. GoogleMaps

Diagnosis. Litoria pinocchio sp. nov can be diagnosed from all other Litoria by the following combination of characters: long (up to at least 2.5 mm), erectile, rostral spike in males that is circular in cross section; relatively small size (SVL 29.2 mm); moderately slender build (HW/SVL 0.26); tibia less than half length of body (SVL/TL 0.48); large eyes (EYE/SVL 0.12); moderately small tympanum (TYM/SVL 0.055); small, rounded, green tubercles present on lateral surfaces of torso but not extending across mid-dorsum; light-brown dorsal colouration with distinct green transverse bands and relatively little dark-brown flecking and spotting; and orange colouration in concealed areas of thighs and axilla.

Description of holotype. Adult male ( Fig. 4 View FIGURE 4 A–B) with vocal slits and pigmented nuptial pads (see Table 1 View TABLE 1 for summary of measurements and ratios). Body slender and elongate, tibia slightly less than half length of body, head much wider than body in dorsal profile, clearly distinct from neck. Snout rounded in dorsal view and truncate in lateral view, with distinct rostral spike extending from tip of upper jaw. Canthus rostralis moderately well defined, slightly curved; loreal region concave. Nares closer to tip of snout (excluding spike) than to eye, oriented laterally, close to top of snout. Eyes large, protruding in both dorsal and lateral views; pupil horizontal. Upper jaw protruding marginally beyond lower jaw. Tympanum moderately small, with a distinct annulus, bordered dorsally by a thick, fleshy supratympanic fold extending to the superior edge of the insertion of the upper arm. Choanae small and circular, situated close to anterior and lateral edge of palate; no vomerine teeth visible; tongue fleshy and ovoid with slightly indented posterior edge. Vocal slits present. Dorsal skin entirely smooth; ventral skin coarsely granular on throat, abdomen and upper hindlimbs; remaining ventral surfaces of limbs smooth; unpigmented ventral tubercles concentrated around vent, along posterior edge of hindlimbs and, to a lesser extent, along posterior edge of forelimbs.

Fingers with relative lengths III>IV>II>I; fleshy, opaque webbing between all digits, forming a narrow basal strip between I and II, extending to disc on distal edge of II and proximal edge of IV, and to penultimate phalanx on both sides on III. Terminal discs expanded, wider than toe discs and with distinct circum-marginal grooves. Nuptial pads brown, roughly tear-shaped with point of tear oriented in posteroventral direction. Indistinct, unpigmented, bifid subarticular tubercle present at base of penultimate phalanx on all fingers, series of further indistinct unpigmented subarticular tubercles present on finger IV, indistinct proximal metacarpal tubercle at base of I, and a pair of smaller distal metacarpal tubercles at base of both III and IV.

Toes moderately long, relative lengths IV>III>V>II>I. All digits with extensive fleshy, opaque webbing, basal between I and II, extending to anterior end of penultimate phalanx on distal edge of II and III and proximal edge of V, to halfway along penultimate phalanx on proximal edge of III and IV, and base of penultimate tubercle on distal edge of IV. Terminal discs slightly expanded, narrower than finger discs and with distinct circum-marginal grooves. Indistinct unpigmented subarticular tubercles on penultimate phalanx of all toes, single on I-III, bifid on IV and V. Small, indistinct unpigmented metatarsal tubercle at base of I.

In preservative, ground colour of all dorsal surfaces light olive green. Dorsum with three indistinct blueishgreen transverse blotches ( Fig. 4A View FIGURE 4 ); anterior and thinnest blotch extending from orbit to orbit, margined posteriorly and anteriorly by ragged, thin, but noticeably darker-blue edges; posterior two blue blotches much larger with indistinct margins, extending across shoulders and posterior half of abdomen respectively, anterior edge of posteriormost blotch also distinctly darker blue. Additional smaller light-blue patches around anterior dorsal edges of elbows and dorsal surfaces of ankles, knees, and groin. Rostral spike and tip of snout predominantly blue. Two prominent white patches on either side of head, extending from eye, curving below tympanum and ending superior to axilla. Limbs with extensive greyish-brown maculations and vermiculations.Venter plain off-white, unpatterned except for sparse brown maculations along the edge of the lower jaw ( Fig. 4B View FIGURE 4 ).

Appearance in life. The following description is based on photographs of the holotype taken at night and during the day ( Fig. 5 View FIGURE 5 A–E). Ground color of dorsal and lateral surfaces medium brown, with extensive vermiculations of darker brown along lateral surfaces. Three prominent, green transverse dorsal bands or blotches, one thin band between anterior edge of eyes, and two much wider and more indistinct bands extending across shoulders and posterior half of abdomen respectively. Further bright-green lateral flecks and blotches along lips, orbit, elbow and hindlimbs. Rostral spike predominately green, with brown flecks and an unpigmented tip. Broken yellowish-white labial stripe extending from tip of snout below eye to axilla. Iris with indistinctly edged outer ring of golden-brown with dark brown flecks, medial ring of dark brown with golden flecks, and narrow golden-brown inner ring around the pupil. Concealed surfaces of fore and hindlimbs orange ( Fig. 5E View FIGURE 5 ). Venter predominately offwhite, heavily flecked with brown around the edges of the lower jaw.

Comparisons with other species. The combination of small adult size (<35 mm), slender build and a rostral spike distinguishes L. pinocchio sp. nov. from all but four other Melanesian Litoria . Of these four taxa L. pinocchio sp. nov. can be distinguished from L. mareku by its larger size (male SVL 29.2 mm vs 25.5–26.5 mm), long erectile rostral spike in males (vs effectively a short stub that is wider than long), and light to medium brown base colouration on dorsum (vs at least some regions of very dark chocolate brown); from L. havina by its mixed green and brown dorsal colouration (vs uniform green or brown) and orange groin colouration (vs red); and from L. mucro (found at lower elevation in the Fojas) by its proportionally shorter legs (TL/SVL = 0.48 vs 0.51–0.56), larger eyes (EYE/SVL = 0.12 vs 0.097–0.11), and more complex dorsal pattern with three prominent green bands (vs predominantly brown or olive-green with at most a small amount of light-green flecking). Males of L. havina and L. mucro also have shorter rostral spikes than L. pinocchio sp. nov. (RL <2.0 mm vs>2.0 mm).

Litoria pinocchio sp. nov. is most similar in size and appearance to L. pronimia from the southern slopes of the Central Cordillera. We compared the single specimen of L. pinocchio sp. nov. with L. pronimia specimens from populations scattered widely across much of its known range. It differs by its shorter limbs (TL/SVL 0.48 vs 0.49– 0.52), wider tympanum (TYM/SVL 0.055 vs 0.042–0.053), and light green tubercles in life prominent on lateral regions of mid-torso but not extending across the dorsum (vs extending across the dorsum at mid-torso). Litoria pinocchio sp. nov. further has a tendency towards a more robust build than L. pronimia (HW/SVL 0.26 vs 0.23– 0.26, with only one specimen out of 23 L. pronimia having the maximum ratio of 0.26). The preserved holotype of L. pinocchio sp. nov. also has a more clearly defined dorsal pattern of blue (green in life) blotches on a light brownish background (see Fig. 4 View FIGURE 4 ) (vs densely ‘peppered’ with varying shades of brown and blue, and with transverse green regions tending to be less clearly defined (see Fig. 2 View FIGURE 2 )). Comparison of colour patterns in life based on a series of photographs of both species also suggests some further differences, with the holotype of L. pinocchio sp. nov. having a broken off-white labial stripe extending from the tympanum and across the front of the snout ( Fig. 5 View FIGURE 5 B–D) (vs absent, or on lateral regions of head only) and no visible off-white tubercles along the outer edge of the lower arms and legs (vs usually apparent).

Etymology. In reference to Carlo Collodi’s fictional character Pinocchio, who had a nose that became longer when under stress or lying.

Range. Litoria pinocchio sp. nov. is known only from a single site on the southern slopes of the Foja Mountains in northern Papua Province, Indonesian New Guinea ( Fig. 3 View FIGURE 3 ). Despite extensive searching over six nights at the same site, and during nearly 6 weeks of surveys across two trips at sites higher (~ 1500 m a.s.l) and lower (~ 700 m a.s.l) than the type locality in the Foja Mountains, we failed to capture further individuals. Litoria pinocchio sp. nov. was also not detected during surveys of the nearby Mamberamo Basin, and locals from the villages of Kwerba and Papasina in foothill forests around the Foja Mountains were unfamiliar with this species, suggesting it does not occur at these lower elevations.

Ecological notes. The holotype was collected in undisturbed mid-montane forest at around 1250 m a.s.l. ( Fig. 6 View FIGURE 6 ). Other Litoria and related genera collected at the type locality were three stream-breeding species: Litoria cf. modica , Litoria cf. arfakiana and Nyctimystes pulcher , and a small green lentic-breeding Litoria species that is currently the subject of taxonomic investigation (S.J. Richards, unpublished).

Conservation status. Litoria pinocchio sp. nov. occurs in a region retaining large areas of undisturbed forest with very low human population density. However given that it is known only from a single specimen and information on its distribution and habitat requirements are lacking, we recommend that it be classified as Data Deficient by the IUCN.

Remarks. The holotype was found on the ground in heavy rain in the late afternoon. When collected, the spike was oriented at 180 degrees to the line of the body ( Fig. 5D View FIGURE 5 ). Subsequent to capture, the spike became less rigid and ‘drooped’ ( Fig. 5A View FIGURE 5 ). A similar transition has been reported and photographed in L. mucro and L. pronimia ( Günther 2014; Menzies & Johnston 2015). No females of L. pinocchio sp. nov. are known; however, based on its close similarity to L. pronimia and other small spike-nosed Litoria , we hypothesize that only males have a spike.

Another small Litoria with a rostral spike was observed at higher elevations in the Foja Mountains on a previous expedition in 2005 at the ‘Bog Camp’ site (~ 1600 m a.s.l.; 2.57°S, 138.72°E). This specimens was calling in an inaccessible position on a leaf in the lower canopy, and we are unable to confirm that it was L. pinocchio sp. nov.

MZB

Museum Zoologicum Bogoriense

Kingdom

Animalia

Phylum

Chordata

Class

Amphibia

Order

Anura

Family

Hylidae

Genus

Litoria