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40 results for “Ceratobatrachidae”
Figure 3 in On the Liurana (Anura: Ceratobatrachidae) of India with the description of three new species from Talley Valley Wildlife Sanctuary in Arunachal Pradesh, Eastern Himalayas
Figure 3. Liurana indica sp. nov. showing the type locality; holotype in live and preserved conditions. Scale is for the preserved specimen photographs only.
Data from: Multilocus phylogeny and a new classification for Southeast Asian and Melanesian forest frogs (family Ceratobatrachidae)
We present a near comprehensive, densely sampled, multilocus phylogenetic estimate of species relationships within the anuran family Ceratobatrachidae, a morphologically and ecologically diverse group of frogs from the island archipelagos of Southeast Asia and the South-West Pacific. Ceratobatrachid frogs consist of three clades: a small clade of enigmatic, primarily high-elevation, semi-aquatic Sundaland species currently assigned to Ingerana (for which we erect a new genus), which is the sister taxon of two large, monophyletic radiations, each situated on islands on either side of Wallace's Line. One radiation is composed of Philippine species of Platymantis and the other contains all taxa from the eastern Indonesian, New Guinean, Solomon, Bismarck, and Fijian archipelagos. Several additional genera (Batrachylodes, Discodeles, Ceratobatrachus, and Palmatorappia) are nested within Platymantis, and of these Batrachylodes and Discodeles are nonmonophyletic. To address the widespread paraphyly of the genus Platymantis and several additional nomenclatural issues, we undertook a wholesale nomenclatural reorganization of the family. Given our partially unresolved phylogeny, and in order to impart a conservative, stable taxonomy, involving a minimal number of genus-species couplet changes, we propose a conservative classification representing a few compromises. These changes are designed to preserve maximally the presumed original intent of taxonomy (widely used group names associated with morphological and ecological diversity of particular species or groups of species) while implementing a hierarchical system that is consistent with the estimate of phylogeny based on new molecular data.
FIGURE 4 in Two new species of Platymantis (Anura: Ceratobatrachidae) from the Admiralty Archipelago, Papua New Guinea
FIGURE 4. Thigh patterns of A. Platymantis admiraltiensis sp. nov. holotype (SAMA R62799), B. P. latro sp. nov. holotype (SAMA R62819) and C. P. papuensis showing distinct mottling of thighs of P. admiraltiensis sp. nov.
FIGURE 5. A in Two new species of Platymantis (Anura: Ceratobatrachidae) from the Admiralty Archipelago, Papua New Guinea
FIGURE 5. A. Platymantis admiraltiensis sp. nov. (SAMA R62802) and B. P. l a t ro sp. nov. (UPNG 10052) in life.
FIGURE 3 in Two new species of Platymantis (Anura: Ceratobatrachidae) from the Admiralty Archipelago, Papua New Guinea
FIGURE 3. Plantar views of A. Platymantis admiraltiensis sp. nov. holotype (SAMA R62799) and B. P. latro sp. nov holotype (SAMA R62819). Scale = 5 mm.
FIGURE 1 in Two new species of Platymantis (Anura: Ceratobatrachidae) from the Admiralty Archipelago, Papua New Guinea
FIGURE 1. Lateral view of heads of A. Platymantis admiraltiensis sp. nov. holotype (SAMA R62799) and B. P. latro sp. nov. holotype (SAMA R62819) showing distinct lateral band of P. latro sp. nov. Scale = 10 mm.
FIGURE 2 in Two new species of Platymantis (Anura: Ceratobatrachidae) from the Admiralty Archipelago, Papua New Guinea
FIGURE 2. Palmar views of A. Platymantis admiraltiensis sp. nov. holotype (SAMA R62799) and B. P. latro sp. nov holotype (SAMA R62819). Scale = 5 mm.
FIGURE 8 in Two new frogs of the genus Platymantis (Anura: Ceratobatrachidae) from the Isabel Island group, Solomon Islands
FIGURE 8. Comparisons of complete calls of sympatric P. parilis (A: 22.1°C) and P. neckeri (B: 22.3°C). Included are 1250–1500 ms audiospectrograms (top panels: frequency in kHz vs. time in ms) and oscillograms (bottom panels: relative amplitude vs. time in ms). Note invariant structure and internote interval in P. parlis (A) versus complex, alternating note structure and declining internote interval across the call of P. neckeri (B).
FIGURE 3 in Two new frogs of the genus Platymantis (Anura: Ceratobatrachidae) from the Isabel Island group, Solomon Islands
FIGURE 3. Photographs of the holotype of P. d e s t i c a n s (A: SAMA R56849) and a paratype of P. parilis (B: SAMA R56908) in life.
FIGURE 6 in Two new frogs of the genus Platymantis (Anura: Ceratobatrachidae) from the Isabel Island group, Solomon Islands
FIGURE 6. The advertisement call of P. desticans (holotype SAMA R56849) recorded at ambient temperature of 24.7°C Barora Faa Island, by SJR. A power spectrum (A: Fast Fourier Transformation; relative amplitude vs. frequency in kHz), a 200 ms audiospectrogram (B: frequency in kHz vs. time in ms), and an expanded waveform (C: relative amplitude vs. time in ms) of a single call. A 2.0 s audiospectrogram (D: frequency in kHz vs. time in ms) and oscillogram (E: relative amplitude vs. time in ms) of a typical pair of calls from the 35 s recording segment waveform depicted in F (showing paired call groups during peak calling activity).
FIGURE 1 in Two new frogs of the genus Platymantis (Anura: Ceratobatrachidae) from the Isabel Island group, Solomon Islands
FIGURE 1. Map of Choiseul and Isabel islands in relation to the Solomon Islands Archipelago (inset), showing type locality of P. desticans new species (triangle: Barora Faa Island, off the western tip of Isabel Island), the type locality of P. parilis (square: Kolopakisa Village, northwestern Isabel Island) and the western Choiseul (circle, Parora River) locality where P. desticans has also been collected.
FIGURE 4 in Two new frogs of the genus Platymantis (Anura: Ceratobatrachidae) from the Isabel Island group, Solomon Islands
FIGURE 4. Oblique views of the heads of the holotypes of (A) P. desticans (SAMA R56849) and (B) P. parilis (SAMA R56911). Scale bars = 5mm.
FIGURE 7 in Two new frogs of the genus Platymantis (Anura: Ceratobatrachidae) from the Isabel Island group, Solomon Islands
FIGURE 7. The advertisement call of P. parilis (holotype SAMA R56911) recorded at ambient temperature of 22.1°C, Kolopakisa Village, Isabel Island, by SJR. (A) a power spectrum (Fast Fourier Transformation; relative amplitude vs. frequency in kHz); a 1.2 s audiospectrogram (B: frequency in kHz vs. time in ms) and an expanded waveform (C: relative amplitude vs. time in ms) of a single call. A 10 s audiospectrogram (D) and oscillogram (E) of a typical pair of calls from the 35 s recording segment waveform depicted in F (showing calls during peak calling activity).
FIGURE 4 in A new species of limestone karst inhabiting forest frog, genus Platymantis (Amphibia: Anura: Ceratobatrachidae: subgenus Lupacolus) from southern Luzon Island, Philippines
FIGURE 4. Oblique view illustration of lateral head of (A) Platymantis (Lupacolus) quezoni, sp. nov., holotype (PNM 9817) and (B) P. dorsalis (KU 300356). Scale bars = 2 mm; Illustrations by M. Garfield.
FIGURE 1 in A new species of limestone karst inhabiting forest frog, genus Platymantis (Amphibia: Anura: Ceratobatrachidae: subgenus Lupacolus) from southern Luzon Island, Philippines
FIGURE 1. Known occurrence of Platymantis (Lupacolus) quezoni, sp. nov., in the Quezon Protected Landscape, southern Luzon Island, Philippines (black dot). The inset shows the location of Luzon Island (darkly shaded) within the Philippines. Note the adjacent position of the Bondoc Peninsula (a geological formation characterized by extensive limestone karst formations; MGB 2010), where we suspect additional P. q u e z o n i populations may occur (see text).
FIGURE 2 in A new species of limestone karst inhabiting forest frog, genus Platymantis (Amphibia: Anura: Ceratobatrachidae: subgenus Lupacolus) from southern Luzon Island, Philippines
FIGURE 2. Ventral views of hand (A) and foot (B) of the adult male holotype of Platymantis (Lupacolus) quezoni, sp. nov. (PNM 9817), and adult male specimens of (C, D) Platymantis dorsalis (KU 300356), (E, F) P. p a e n g i (KU 300206), and (G, H) P. spelaeus (KU 300438) for comparison. Scale bars = 2 mm.
FIGURE 6 in A new species of limestone karst inhabiting forest frog, genus Platymantis (Amphibia: Anura: Ceratobatrachidae: subgenus Lupacolus) from southern Luzon Island, Philippines
FIGURE 6. Advertisement call of Platymantis quezoni, sp. nov. An expanded audiospectogram and waveform (A: frequency [kHz] vs. time [ms]); the Fast-Fourier Transformation (B: Power spectrum of A: relative amplitude vs. frequency); a 3-call non-expanded oscillogram (C: relative amplitude vs. time) and the corresponding sonogram (D: audiospectrogram, frequency vs. time). Note alternating frequency sweep calls of P. dorsalis between those of P. quezoni, and constant ambient background vocalizations of cicadas (4–5 kHz) in Fig. D.
FIGURE 3 in A new species of limestone karst inhabiting forest frog, genus Platymantis (Amphibia: Anura: Ceratobatrachidae: subgenus Lupacolus) from southern Luzon Island, Philippines
FIGURE 3. Photographs of the (A) Platymantis (Lupacolus) quezoni, sp. nov., holotype (PNM 9817; SVL = 33.7) and (B) a male paratype (KU 328735; SVL = 31.3). Photos: RMB.
FIGURE 5 in A new species of limestone karst inhabiting forest frog, genus Platymantis (Amphibia: Anura: Ceratobatrachidae: subgenus Lupacolus) from southern Luzon Island, Philippines
FIGURE 5. Limestone karst forest habitat of Platymantis (Lupacolus) quezoni, sp. nov., at the type locality: (A) limestone bolder where the holotype (PNM 9817) was recorded and collected; (B) appearance of habitat in late afternoon (~16:30). Note darkened caves and crevices beneath limestone over-hangs from where P. q u e z o n i initiate vocalizations in the late afternoons (16:30–17:30 hr) from concealed perches inside crevices and small caves. Photos: RMB.
FIGURE 1 in A new miniature Melanesian Forest Frog (Ceratobatrachidae: CORNufeR) from New Britain Island, constituting the first record of the subgenus BATRAchylOdes from outside of the Solomon Archipelago
FIGURE 1. Map of the Bismarck and Solomon Archipelagos showing the distributions of all species of Cornufer within the subgenus Batrachylodes, including the type locality of Cornufer exedrus (black circle) at Tompoi Camp (~1,600 m above sea level) in the Nakanai Mountains of eastern New Britain.
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