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Fig. 2 in A new species of terrestrial-breeding frog of the genus Psychrophrynella (Anura: Strabomantidae) from the Cordillera de Vilcabamba, southeastern Peru

Fig. 2. Photographs in life of paratypes of Psychrophrynella vilcabambensis sp. nov. (A–B) Dorsolateral and ventral views of adult female, MUBI 13486 (SVL = 16.63 mm); (C–D) dorsolateral and ventral views of juvenile MUBI 13484 (SVL = 12.99 mm).

Fig. 4 in A new species of terrestrial-breeding frog of the genus Psychrophrynella (Anura: Strabomantidae) from the Cordillera de Vilcabamba, southeastern Peru

Fig. 4. Map of Peru indicating the type localities of species of Psychrophrynella and Noblella from the southeastern region of the country.

Fig. 1 in A new species of terrestrial-breeding frog of the genus Psychrophrynella (Anura: Strabomantidae) from the Cordillera de Vilcabamba, southeastern Peru

Fig. 1. Photographs in life of the holotype of Psychrophrynella vilcabambensis sp. nov., adult male MUBI 13485 (SVL = 16.5 mm.). (A–B) Dorsolateral views; (C) ventral view.

Fig. 3 in A new species of terrestrial-breeding frog of the genus Psychrophrynella (Anura: Strabomantidae) from the Cordillera de Vilcabamba, southeastern Peru

Fig. 3. Morphological details of Psychrophrynella vilcabambensis sp. nov. (A) Plantar surface with a red arrow indicating the presence of lateral fringes (MUBI 13484); (B) lateral view of forelimb with white arrows indicating the presence of ulnar tubercles (MUBI 13485).

opencc-by-4.0Jun 2020View details →

Fig. 1 in Cultural association and its role in garnering support for conservation: the case of the Mountain Chicken Frog on Dominica

Fig. 1. The Commonwealth of Dominica, and its position in the Caribbean, showing the distribution of Leptodactylus fallax and the study locations (After Adams et al. 2014; IUCN SSC Amphibian Specialist Group 2017).

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Fig. 4. Forest Islands 1, 2 in The Blue Dyeing Poison-Dart Frog, Dendrobates tinctorius (Dendrobates azureus, Hoogmoed 1969): extant in Suriname based on a rapid survey

Fig. 4. Forest Islands 1, 2, and 4, extant vegetation comparison between Google Earth images for 2004 (A) and 1969 (B). Red outlines delineating the three forest islands were juxtaposed from the 2004 image onto the 1969 image.

opencc-by-4.0Dec 2019View details →

Fig. 1 in The Blue Dyeing Poison-Dart Frog, Dendrobates tinctorius (Dendrobates azureus, Hoogmoed 1969): extant in Suriname based on a rapid survey

Fig. 1. Map of Suriname, South America (upper left inset) with approximate location of Sipaliwini savannah indicated by the black box. Forest Islands are outlined in red and identified by numbers corresponding to those of Hoogmoed (1969, 2019). Arrows indicate locations of the 50 x 50 m plots surveyed in Forest Islands 1, 2, and 4 during 16–18 June 2015. Forest Island 3 was not surveyed. In this 2004 Google image, savanna vegetation surrounding the forest islands had been recently burned by indigenous hunters.

Fig. 4 in Breeding and rearing the Critically Endangered Lake Oku Clawed Frog (Xenopus longipes Loumont and Kobel 1991)

Fig. 4. Monthly water temperatures (circles) and pH (triangles) recorded from the shoreline of Lake Oku between 2008/2009 and 2013. Error bars represent SEM.

Fig. 1 in Breeding and rearing the Critically Endangered Lake Oku Clawed Frog (Xenopus longipes Loumont and Kobel 1991)

Fig. 1. Male (top) and female (bottom) adults of Xenopus longipes in the collection at ZSL London Zoo (ZIMS ID 7441).

Fig. 3. Aquarium for X. longipes, set within a in Breeding and rearing the Critically Endangered Lake Oku Clawed Frog (Xenopus longipes Loumont and Kobel 1991)

Fig. 3. Aquarium for X. longipes, set within a custom built, centrally filtered system (inset photograph) at ZSL London Zoo. Life support system and sump not shown – see text for details.

Fig. 2 in Breeding and rearing the Critically Endangered Lake Oku Clawed Frog (Xenopus longipes Loumont and Kobel 1991)

Fig. 2. Keratinized nuptial pads on the inside surfaces of the front limbs of male (A and C) and cloaca of a female X. longipes (B); note the cloacal papillae, which are absent in male frogs.

Fig. 5 in Breeding and rearing the Critically Endangered Lake Oku Clawed Frog (Xenopus longipes Loumont and Kobel 1991)

Fig. 5. Gosner stage progression of the most rapidly developing X. longipes tadpole. Hatching to metamorphosis took 193 days, but smaller tadpoles had only reached stage 35 by this point.

Fig. 5. A in Two new species of frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from the Peruvian Andes

Fig. 5. A) Habitat of the type locality of Phrynopus valquii sp. nov.; B) Microhabitat of Phrynopus valquii sp. nov.; C) Habitat of the type locality of Phrynopus daemon sp. nov.; D) Microhabitat of Phrynopus daemon sp. nov. Photographs: A–B by Germán Chávez and C–D by Roy Santa-Cruz.

Fig. 3 in Two new species of frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from the Peruvian Andes

Fig. 3. Distribution of Phrynopus valquii sp. nov. (green circles) and Phrynopus daemon sp. nov. (red circles). Map by Ca- terina H. Cosmopolis.

Fig. 4 in Two new species of frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from the Peruvian Andes

Fig. 4. Dorsal (left) and ventral (right) views of the type series of Phrynopus daemon sp. nov.: A–B) Holotype (CORBIDI 15364, adult female, SVL = 24.3 mm); C–D) Female paratype (MUSA 4916, adult female, SVL = 21.4 mm); E–F) Male paratype (MUSM 32747, SVL = 21.7). Photographs: A–D by Roy Santa-Cruz and E–F by Daniel Rodriguez.

Fig. 2 in Two new species of frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from the Peruvian Andes

Fig. 2. Ventral view of: A) right hand of the holotype of Phrynopus valquii; B) right foot of the holotype of Phrynopus valquii; C) right hand of the holotype of Phrynopus daemon; D) right foot of the holotype of Phrynopus daemon. Photographs by Germán Chávez.

Fig. 1 in Two new species of frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from the Peruvian Andes

Fig. 1. Dorsal (left) and ventral (right) views of specimens of the type series of Phrynopus valquii sp. nov.: A–B) Holotype (COR- BIDI 14005, adult female, SVL = 31.2 mm); C–D) Paratype (CORBIDI 14007, adult female, SVL = 28.07 mm); E–F (CORBIDI 13993, adult male, SVL = 25.2 mm). Photographs by Germán Chávez.

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Fig. 4 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites

Fig. 4. Mature sporocysts of Hyaloklossia in the kidney of Pelophylax porosus porosus. (A) Light microscopy of a mature sporocyst in homogenized kidney tissue. (B) Nomarski interference contrast microscopy of a mature sporocyst in squash preparation of renal tubular tissue showing the presence of four spindle-shaped sporozoites. (C) Composite line drawing. Bar = 10 μm. Asterisk: sporocyst residuum.

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Fig. 3 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites

Fig. 3. Light microscopy of hematoxylin and eosin-stained sections of renal tissues of Pelophylax porosus porosus. (A) Mature sporocysts in the renal interstitium. Arrows indicate the transverse section of sporocysts showing four sporozoites with nuclei and a granular sporocyst residuum. (B and C) Immature oocysts. Note the very thin oocyst wall (arrows), sporonts with granular cytoplasm, and nuclei distributed at the cell margin (arrowheads). (D) Immature oocysts with two sporoblasts each and containing two polar nuclei (arrowheads). (E) Mature oocysts in renal epithelial cell showing two sporocysts with elongated sporozoites with circular nuclei (arrowhead) and a granular sporocyst residuum. Arrows indicate the sporocyst wall. Bars = 50 μm (A) and 10 μm (B–E).