Bioacoustics of Kalophrynus cryptophonus

Species

Account

What the sources say about this taxon, as written.

distribution · Plazi

DISTRIBUTION .— Vietnam . Kalophrynus cryptophonus is known only from the vicinity of the type locality . NATURAL HISTORY .— This sticky frog lives in a mid-montane evergreen tropical forest (secondary) with abundant bamboo clumps. It was discovered in mid April by the males’ vocalization from inside cut bamboo stems. The water inside the bamboo stems serve as egg-deposition and larval development sites (phytotelm breeding).

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etymology · Plazi

ETYMOLOGY .— Because this species was only discovered by the males’ vocalization from hollow bamboo stems, the authors highlight this behavior with Greek cryptos for hidden or mystery and phonus , voice, thus hidden voice.

this account at Plazi

etymology · Plazi

Etymology. The species name is a noun in the nominative case, derived from the Greek cryptos, meaning “to hide”, “mystery”, “cryptic”, and phonus meaning “voice” in reference to our history of discovering the species. During the expedition of the JRVTRTC in April–May, 2013 in Loc Bao forest, Lam Dong Province, we recorded unusual frog calls which were hard for us to locate. After two weeks of searching we found a male Kalophrynus cryptophonus sp. nov. calling from an empty bamboo stem. Recommended vernacular name: The recommended common name in English is Bamboo sticky frog, referring to the unusual breeding habitat of the new species.

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description · Plazi

Description of holotype . Adult male ( Fig. 3 AB) with well-developed oblong testes; measurements are given in Table 4. Habitus stout, with body widest in lumbar area. Head relatively short (HL/SVL 0.31), slightly wider than long (HL/HW 0.88), triangular. Snout pointed, short (SL/HL 0.36), sloping in profile ( Fig. 3 C) and distinctly projecting beyond lower jaw; canthus rostralis indistinct, smooth; nostrils rounded, situated closer to snout tip than to eye (SND/ END 0.65) and oriented rostrolaterally. Eyes bulging, medium-sized (ED/SVL 0.11), lateral, well visible from below, with oval horizontal pupil; upper eyelid with fine tubercles on margin, UEW/IOD 0.45. Tympanum very close to eye, smaller than eye (TD/ED 0.69, TD/SVL 0.08), roughly round, distinct, bordered from above by sharply prominent supratympanic fold running from posterior corner of eye along upper edge of tympanum and then down to the point of forelimb insertion. Maxillary and vomerine teeth absent; tongue with even rounded edge posteriorly; transversal crenulated dermal ridge on palate posterior to eyes level, short low dermal fold anterior to it, restricted to medial part of palate; postchoanal dermal ridges distinct. Small notch in the rostral part of skin covering of upper jaw and small prominence on the rostral part of lower jaw, fitting together. Single subgular vocal sac; wide slit-like vocal openings between jaw articulation and tongue insertion. Numerous tubercles with wide base and sharp, conical, semitransparent apical spine being clearly distinct on skin covering maxilla and mandible ( Fig. 3 D). Spines on mandible largest, bordering the lower jaw in one to three rows, from rostral end to mouth corner and spreading on the area below and behind tympanum; on upper jaw spines smaller and occupying the entire area below snout tip, nostrils and eyes. Several tiny, hardly distinct similar spines present on each tympanum. Small scattered spines spread on axillar area, on anterior forelimb surface and on breast between forelimbs, but not on gular region. Forelimbs slender, more than half of body length (FLL/SVL 0.71); hands with rudimental webbing. Tips of fingers rounded, without dilatation. Relative length of fingers I<IV<II<III; palmar tubercle moderately large, prominent, oval in shape; subarticular tubercles prominent, rounded; one on each fingers I, II and IV and two on finger III; smaller additional metacarpal tubercles between palmar tubercle and each finger base ( Fig. 4 A). Nuptial pads on dorsal hand well-defined, finely asperous, thickened areas of skin covering fingers I–III from base to proximal end of terminal phalange ( Fig. 4 C). Hind limbs slender, relatively short (HLL/SVL 1.36); when legs adpressed to body laterally, heel reaches interval between eye and tympanum. Tibia slightly shorter than thigh (TFL/ThL 0.96) and significantly shorter than tarsus+foot (TFL/TarFL 0.66). Toe tips rounded, without dilatation; relative length of toes I<II<V<III<IV; foot webbing formula I 1–2 ½ II ½–2½ III 1 ½ –3½ IV 3 ¾–1½ V ; subarticular tubercles moderately prominent on toes I–IV, oval in shape; one on each toe I and II, two on toe III and three on toe IV; distal subarticular tubercle on toe V distinct, proximal one less conspicuous, rudimentary; inner metatarsal tubercle prominent, oval; outer metatarsal tubercle smaller than inner one (OMTL/IMTL 0.8), low, rounded ( Fig. 4 B). Skin on dorsum finely shagreened from interorbital level to vent, with singular small tubercles topped with tiny apical spine; smooth on the snout; roughly granular on belly, lower flanks, thighs undersides and in cloacal region, smooth on gular area, inner leg surfaces and forelimbs except for scarce, tiny spines in outer and axillar surfaces. Two pairs of whitish glandular tubercles on the pectoral region, each with tiny sharp spines on apex. Dorsolateral boundary sharp, finely glandular. Coloration. In life,( Fig. 5 AB) ground coloration on upper head, trunk and limb surfaces variable, ranging from chocolate-brown at night to pinkish-beige during the day time. Sharp edge of dorsal coloration extending from snout tip through upper eyelid to groin contrasted by darker, pinkish-brown flanks and head sides. Diffuse pinkish-gray pattern in the shape of inverted “ Y ” on the dorsum lasting from interorbital area towards inguinal region and edged with light-beige color. " Y "-shaped pattern followed laterally by three less distinct, parallel, intervening stripes forming somewhat reticulate pattern. Pale rounded spot visible on parietal area, similar diffuse spots scattered on dorsum. Three faint brownish crossbands on thigh and shin; brown marmorate pattern on elbow and knee, on foot underside and on anterior surface of lower forearm and hand. Cloacal region brownish, separated from dorsal surface by thin pale edging line. Inguinal ocelli represented by small (smaller than tympanum, ISD/TD 0.77) rounded black spot in each inguinal area, without light edges; three asymmetric small dark dots on left side of back. Venter pale, yellowish-pink, unpatterned except for gular, chest and upper belly areas displaying diffuse brownish-gray spotting; palmar and plantar surfaces pink. Iris golden. In preservative coloration fades to gray on dorsum and flanks and yellowish-gray on venter; other features remain without significant change. Variation. Individuals of the type series are similar in morphology, body size and proportions (Table 4; Fig. 3 E), except for the female that is smaller in size and lacks the spines and the asperous patches on the hand. The spines in males vary slightly in abundance and size; in all individuals they are the largest on mandible margins, especially in the subtympanal area, and may be less conspicuous on the upper jaw. Nuptial pads on fingers I–III are similar in all males. Variations in the coloration include the inverted “ Y ” or hourglass-shaped pattern on dorsum, which may be almost indistinct; three paratypes have a uniform stellar, slightly paler pattern on back. The inguinal ocelli vary in size, but are always smaller in diameter than tympanum (ISD/TD 0.77±0.05); in the female this spot is present only on the left side of body. Supernumerary asymmetric small dark spots may occur in the inguinal area, on back and on upper thigh and shin surface. The female ( Fig. 5 CD) additionally differs in undersides coloration by having a more pronounced dark marbling or spotting on the upper belly and lower part of flanks, and by having a light medial band on the gular surface bordered with diffuse brown blotches. The ovaries of the female contain relatively small quantity (50–60 per ovary) of developing unpigmented eggs variable in size (diameter 0.3–0.9 mm ). Natural history. All specimens were collected at night time on the limited parcel of secondary, disturbed mountain high polydominant evergreen tropical forest with the abundance of bamboo Phyllostachys sp. ( Poaceae ) ( Fig. 6 ), where Kalophrynus cryptophonus sp. nov. occurs syntopically with Kurixalus sp., Theloderma bambusicola Orlov, Poyarkov, Vassilieva, Ananjeva, Nguyen, Sang & Geissler , Microhyla fissipes Boulenger , Limnonectes limborgi (Sclater) , and Ingerophrynus galeatus (Günther) . The female was found on the ground; all males were collected while calling from inside dead bamboo stems with diameters of about 30–40 mm ( Fig. 5 E), sometimes as close to each other as 5–10 m ; up to four males were heard simultaneously from one point. Tadpoles were collected on 22 April 2013 in a decaying bamboo stem with diameter about 35 mm . In total, 11 early-stage larvae (Gosner Stage 25) were recorded in one partly perforated internode, containing 70–80 ml of rainwater. A calling male was found in the adjacent internode of the same stem. Tadpole description. Tadpoles were allocated to the species based on the following evidence: (1) morphological features characteristic for microhylid larvae in general and other phytotelm breeding Kalophrynus species in particular (see Discussion); (2) specific site of collection (water-filled decaying bamboo internode) which was close to calling male found in the same bamboo stem; (3) all other phytotelm breeding frogs known from the region (members of the genera Theloderma and Rhacophorus , Rhacophoridae ) differ in tadpole morphology and cannot be mistaken with larvae of the new species. Standard tadpoles measurements (mean±SD, n=4, Stage 25): TL 9.14±0.77; BL 2.50±0.05; BW 1.47±0.03; SVL 3.02±0.16; SSp 1.89±0.15; IOD1.05±0.03; SED 0.98±0.03; ED= 0.16±0.01; ODW= 0.94±0.06; TaL= 6.6±0.72; TH= 0.89±0.1. In dorsal view ( Fig. 7 A), body oval or slightly pyriform, with maximum width at eye level (BW/BL 0.59±0.01); snout long (SED/BL 0.39±0.01), broad, blunt. In lateral view ( Fig. 7 B), body compressed dorsoventrally (BH/BW 0.66±0.05), especially anteriorly, flattened above and convex below. Tail long (TaL/ BL2.70±0.25), lanceolate; almost equal in height along its length; tail tip bluntly acuminate, without terminal filament; muscular part moderately developed; at vent level, tail muscular portion about three times higher than lower fin. Upper fin originating slightly behind body-tail junction, much shorter than the lower fin proximally and nearly equal in height to it distally. Eyes dorsolateral, not visible from below, small (ED/BL 0.06±0.002), pupils oriented dorsolaterally. Nostrils not opened at the stages under description. Spiracle ventral, medial, with short free flap, opening at 0.80±0.06 of distance from snout tip to body end. Vent tube medial, long, directed obliquely backward, with opening at ventral edge of lower fin. Lateral line system not visible. Mouth terminal, oral disk wide (ODW/BW 0.64±0.05), without keratinized elements and obvious papillae. Upper labium widely arched, slightly overhanging Ω-shaped lower labium. Live tadpoles appeared almost unpigmented, whitish, with darker gut and reddish gills clearly visible through translucent skin. In preservative, scattered melanophores visible on the dorsal surface of body and tail. Belly and tail fins totally transparent. Eyes black. Gut forming three wide loops. Call characteristics. The advertisement call of Kalophrynus cryptophonus sp. nov. recorded at 25ºC is represented by rhythmic, non-modulated, tonal calls ( Fig. 8 A). Call duration varied from 42 to 114 ms (79±13ms, n=105). The interval between successive calls in one individual varied from 5.91 to 25.57 s (11.76± 6.57 s , n=10). In two individuals calling simultaneously at the distance 5 m apart from each other the interval between calls uttered by different males varied from 0.009 to 2.37 s (1.06± 0.56 s , n=31). The call repetition rate in individuals (n=11) varied from 0.016 to 0.42 calls per second (0.13±0.12, n=105 calls). The call repetition rate in choruses (n=3) consisting of 4–5 individuals varied from 0.21 to 0.74 calls per seconds (0.44±0.27). The initial (1020±100 Hz) and final fundamental frequency in a single call (920±130 Hz) were almost equal (n=38). Two lower harmonics were distinguishable on the majority of call spectrograms. The maximum amplitude frequency in individual calls (1100±370 Hz, n=38) coincided with the fundamental frequency. The entire call was pulsed, with2–5 pulses (3.270.69, n=52) per call and a mean pulse period of 24±0.3 ms. In all calls recorded the pulse rate varied from 30.3 to 55.6 pulses per second (42.51±6.29 pulses/s, n=52). Comparison. In southern Vietnam , Kalophrynus cryptophonus sp. nov. co-occurs with Kalophrynus interlineatus , which inhabits diverse kinds of forested biotopes at elevations up to 900 m a.s.l. The latter was reliably recorded from the same province and district as Kalophrynus cryptophonus sp. nov. , and both species may potentially occur syntopically with each other. From southern Vietnamese K. interlineatus , the new species differs morphologically by the following features: a smaller size (SVL 23.4–30.4 mm vs. 38.6–45.4 mm ); the presence of skin spines on head and nuptial pads on fingers in males (absent in K. interlineatus ); smooth canthus rostralis (vs. sharp in K. interlineatus ); skin on gular area smooth (roughly tuberculated in K. interlineatus ); longer legs (HLL/ SVL 1.35±0.05 vs. 1.16± 0.07 in K. interlineatus ), in adpressed leg heel reaching tympanum (vs. not reaching tympanum in K. interlineatus ); the presence of rudimental webbing on fingers (absent in K. interlineatus ) and slightly less extensive webbing on toes (webbing formula I 1–2 ½ II ½–2½ III 1 ½ –3½ IV 3 ¾–1½ V vs. I ½ –2 II 1–2 ½ III 1–3 IV 3 ¾– 1 V in K. interlineatus , Fig. 10 CD), and reduced anterior palatal dermal ridge (well developed, arch-shaped in K. interlineatus ). In coloration, Kalophrynus cryptophonus sp. nov. differs from K. interlineatus by having a very small, rudimentary black spot without light edging in inguinal area (smaller than tympanum, ISD/TD 0.77±0.05 vs. larger than tympanum, ISD/TD 1.60±0.36), and white-edged inguinal ocellus in K. interlineatus . In reproductive characteristics, Kalophrynus cryptophonus sp. nov. differs from K. interlineatus by having unpigmented eggs (vs. pigmented in K. interlineatus ). In vocalization, Kalophrynus cryptophonus sp. nov. differs from K. interlineatus by calling from inside bamboo stems (vs. from forest floor, often in dense choruses around breeding ponds), as well as call duration, inter-call interval, frequency and other acoustic parameters ( Fig. 8 AB, Table5). From its other congener, described herein from southern Vietnam , Kalophrynus honbaensis sp. nov. (see below), Kalophrynus cryptophonus sp. nov. differs morphologically by having a smaller body size in males (SVL 27.9–30.4 mm vs. 26.7–36.8 mm in Kalophrynus honbaensis sp. nov. ); large skin spines on head (vs. only microscopic spines in Kalophrynus honbaensis sp. nov. ), nuptial pads on fingers in males present (absent in males Kalophrynus honbaensis sp. nov. ); a smooth canthus rostralis (vs. sharp in Kalophrynus honbaensis sp. nov. ); reduced anterior palatal dermal ridge (vs. well developed, parallel to posterior ridge in Kalophrynus honbaensis sp. nov. ), and more extensive webbing on toes (webbing formula I 1–2 ½ II ½–2½ III 1 ½ –3½ IV 3 ¾–1½ V vs. I 1–2 II 1 ½ –3 III 2–3 ¾ IV 4–2 V ). In coloration, Kalophrynus cryptophonus sp. nov. differs from Kalophrynus honbaensis sp. nov. by having a very small, rudimentary black spot in inguinal area (smaller than tympanum, ISD/ TD 0.77±0.05, vs. larger than tympanum, ISD/TD 1.47±0.09).

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Sources

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SourceIts nameIts rankIts familyRecord
PlaziKalophrynus cryptophonusSpeciesMicrohylidaePlazi/Kalophrynus cryptophonus

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Bioschemas Taxon, as embedded
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