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Fig. 1 in Helminth community structure in two species of arctic-breeding waterfowl

Fig. 1. Study sites in Alaska where Pacific black brant and greater white-fronted geese were collected for helminth examination in 2014; A) Yukon-Kuskokwim Delta (61ǫ N 164ǫ W) in Subarctic western Alaska and B) the Arctic Coastal Plain (70ǫ N 154ǫ) in Arctic Alaska.

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COMMENTS.— Although not breeding in the Mediterranean, the species forages in Libyan waters (van Dijk et al. 2014). In addition to the single beached record, an individual was pulled from nearshore waters of the Tajura coast in 1996 and died in the rehabilitation facility of the Marine Biology Research Centre (MBRC) at Tajura, where it was subsequently taxidermied at the MBRC Museum (Hamza 2010). Capra's (1949) records were based on a report in "L'Idea Coloniale" for 2 May 1927 (Mongàr) and an unspecified specimen in the Museo Civico di Storia Naturale di Trieste (Sella). IUCN THREAT STATUS.— Vulnerable A2bd. MAP 3. Distribution of Dermochelys coriacea in Libya showing stranding site records. in Atlas of the Reptiles of Libya

COMMENTS.— Although not breeding in the Mediterranean, the species forages in Libyan waters (van Dijk et al. 2014). In addition to the single beached record, an individual was pulled from nearshore waters of the Tajura coast in 1996 and died in the rehabilitation facility of the Marine Biology Research Centre (MBRC) at Tajura, where it was subsequently taxidermied at the MBRC Museum (Hamza 2010). Capra's (1949) records were based on a report in "L'Idea Coloniale" for 2 May 1927 (Mongàr) and an unspecified specimen in the Museo Civico di Storia Naturale di Trieste (Sella). IUCN THREAT STATUS.— Vulnerable A2bd. MAP 3. Distribution of Dermochelys coriacea in Libya showing stranding site records.

Fig. 6 in Larval development and breeding ecology of Ziegler's Crocodile Newt, Tylototriton ziegleri Nishikawa, Matsui and Nguyen, 2013 (Caudata: Salamandridae), compared to other Tylototriton representatives

Fig. 6. Tylototriton ziegleri larvae from Bao Lac district, Cao Bang Province with indication of the corresponding developmental stage and scale. Photographs of stages 27 to 36 are from preserved eggs photographed under a digital microscope (photos C. Michel) and photographs of stages 44 and 45 are from individuals in life kept at the Me Linh station (photos T. Ziegler).

Fig. 4 in Larval development and breeding ecology of Ziegler's Crocodile Newt, Tylototriton ziegleri Nishikawa, Matsui and Nguyen, 2013 (Caudata: Salamandridae), compared to other Tylototriton representatives

Fig. 4. Drawing of a formol-preserved larva of Tylototriton ziegleri at stage 35. Drawing C. Michel.

Fig. 2 in Larval development and breeding ecology of Ziegler's Crocodile Newt, Tylototriton ziegleri Nishikawa, Matsui and Nguyen, 2013 (Caudata: Salamandridae), compared to other Tylototriton representatives

Fig. 2. Percentage of the number of adults of Tylototriton vietnamensis and T. ziegleri found at each interval of percentage of canopy cover measured above the water of the breeding site.

Fig. 5 in Larval development and breeding ecology of Ziegler's Crocodile Newt, Tylototriton ziegleri Nishikawa, Matsui and Nguyen, 2013 (Caudata: Salamandridae), compared to other Tylototriton representatives

Fig. 5. Metamorph of Tylototriton ziegleri at stage 44, with an additional finger on left hand, collected in Ha Giang Province in 2012 and preserved in ethanol. Photo M. Bernardes.

Fig. 1. A in Larval development and breeding ecology of Ziegler's Crocodile Newt, Tylototriton ziegleri Nishikawa, Matsui and Nguyen, 2013 (Caudata: Salamandridae), compared to other Tylototriton representatives

Fig. 1. A. Adult male of Tylototriton ziegleri; B. Habitat type in Bao Lac district, Cao Bang Province; C. Adult male of Tylototriton vietnamensis; D. Habitat type in Tay Yen Tu Nature Reserve, Bac Giang Province. Photos M. Bernardes.

Fig. 7 in Larval development and breeding ecology of Ziegler's Crocodile Newt, Tylototriton ziegleri Nishikawa, Matsui and Nguyen, 2013 (Caudata: Salamandridae), compared to other Tylototriton representatives

Fig. 7. Dark and light phenotypic variations of Tylototriton vietnamensis found at the type locality. Photo M. Bernardes.

Fig. 3. A in Larval development and breeding ecology of Ziegler's Crocodile Newt, Tylototriton ziegleri Nishikawa, Matsui and Nguyen, 2013 (Caudata: Salamandridae), compared to other Tylototriton representatives

Fig. 3. A: Typical clutch of Tylototriton ziegleri composed by single eggs; B: an exceptional case of "stickiness" where eggs were aggregated in groups of 2–4. Photos M. Bernardes.

Fig. 3 in New records, range extension and call description for the stream-breeding frog Hyloscirtus lascinius (Rivero, 1970) in Venezuela

Fig. 3. Habitat of Hyloscirtus lascinius at Campamento Guacharaca, Sierra de Perijá, Zulia state (A). Males calling from a branch; (B) and from a rocky wall; (C) at the edge of the creek in Campamento Guacharaca. Photos: F.J.M. RojasRunjaic.

Fig. 2 in New records, range extension and call description for the stream-breeding frog Hyloscirtus lascinius (Rivero, 1970) in Venezuela

Fig. 2. Distribution of Hyloscirtus lascinius in Venezuela and Colombia. 1: Campamento Guacharaca, Sierra de Perijá, Zulia state, Venezuela. 2: San Luis, Mérida state, Venezuela. 3: Road Santa Cruz de Mora-La Macana, Mérida state, Venezuela. 4: Quebrada Ovalles, Mérida state, Venezuela. 5: Quebrada De La Rana, Mérida state, Venezuela. Yellow triangle: Tabor, Tamá massif, Táchira state, Venezuela (type locality); White pentagon: Chinácota, Norte de Santander department, Colombia (Sánchez 2010); The record of headwaters of Río Táchira, Norte de Santander, Colombia (Ruiz-Carranza et al. 1996) and additional localities between Delicias and Tabor (Rivero 1970) are included in the yellow triangle that indicates the type locality.

Fig. 1 in New records, range extension and call description for the stream-breeding frog Hyloscirtus lascinius (Rivero, 1970) in Venezuela

Fig. 1. Hyloscirtus lascinius from Venezuela. (A) Campamento Guacharaca, Sierra de Perijá, Zulia state; (B) Near La Macana, Mérida state; (C) Quebrada La Rana, Mérida state. Photos: F.J.M. Rojas-Runjaic (A) and C.L. Barrio-Amorós (B and C).

Fig. 9 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships

Fig. 9. Habitat of Pristimantis marmoratus (Boulenger, 1900). Left. Submontane rainforest in Kaieteur National Park at ca 630 m elevation. Right. Montane rainforest on the slopes of Maringma-tepui, Guyana at ca 1376 m elevation. Photographs by PJRK.

Fig. 8 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships

Fig. 8. Vocalization of Pristimantis marmoratus (Boulenger, 1900); oscillogram and spectrogram obtained using Seewave v. 1.6.4 in R. Spectrogram (top) and oscillogram (below) of one call of IRSNB 14472 from Kaieteur National Park, Guyana. Call recorded at a temperature of 24°C.

Fig. 6. A in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships

Fig. 6. A. Guzmania cf. sphaeroidea (André) André ex Mez, an arboreal bromeliad species used as egg deposition site by Pristimantis marmoratus (Boulenger, 1900) in the Wokomung Massif. B. Egg clutch of Pristimantis marmoratus deposited on a leaf of the arboreal bromeliad Guzmania cf. sphaeroidea in the Wokomung Massif. C. Egg clutch of Anomaloglossus beebei (Noble, 1923) (white arrow) deposited in the phytotelmata of the same plant as in B. D. Dorsolateral view of IRSNB 17916, 11.3 mm SVL, a juvenile of P. marmoratus collected on the slopes of Maringma-tepui, Guyana. Photographs A–C by DBM, D by PJRK.

Fig. 5 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships

Fig. 5. Pristimantis marmoratus (Boulenger, 1900). Intraspecific variation in dorsal (top) and ventral (below) colour patterns in preserved specimens. Photographs by PJRK.

Fig. 4 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships

Fig. 4. Pristimantis marmoratus (Boulenger, 1900) (four individuals at the top) and P. pulvinatus (Rivero, 1968) (two individuals below). Intraspecific variation in dorsal colour pattern and sexual dimorphism in living specimens. Note: the subtle hint of green visible on the lower body and legs of some specimens of P. marmoratus is due to a reflection of the substrate (green leaf). Photographs by PJRK, except the uncollected P. pulvinatus, which is by CBA.

Fig. 3 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships

Fig. 3. Pristimantis marmoratus (Boulenger, 1900). Ventral view of left hand and left foot of a male (top), and ventral view of right hand and right foot of a female (below), both from Kaieteur National Park, Guyana. Photographs by PJRK.

Fig. 2 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships

Fig. 2. Pristimantis marmoratus (Boulenger, 1900). Preserved adult ♂, holotype (BMNH 1947.2.16.92). A. Dorsal view. B. Ventral view. C. Dorsolateral view. Grid squares = 5 mm. Photographs by PJRK.

Fig. 10 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships

Fig. 10. Phylogenetic relationships within the Pristimantis "unistrigatus group" in the Guiana Shield as recovered in the MrBayes analysis (438 bp of the 16S rRNA gene sequence). Values at each node represent statistical support (* = 0.99 or 1). Pristimantis marmoratus (Boulenger, 1900) is highlighted in red.