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FIG. 8 in An inventory of Bramble sharks Echinorhinus brucus (Bonnaterre, 1788) (Elasmobranchii, Echinorhinidae) in natural history collections worldwide for conservation status assessment

FIG. 8. — Echinorhinus brucus (Bonnaterre, 1788) in Australian (Melbourne) collections (continuation): A, NMV 51369 (Entry 7); B, C, NMV A15734 (Entry 8).

FIG. 17 in An inventory of Bramble sharks Echinorhinus brucus (Bonnaterre, 1788) (Elasmobranchii, Echinorhinidae) in natural history collections worldwide for conservation status assessment

FIG. 17. — Echinorhinus brucus (Bonnaterre, 1788) in French (Ergué-Gabéric and Bayonne) collections: A, GAB-MOO unregistered (Entry 64); B, MHNB 2013.0.162 (Entry 65).

FIG. 6 in An inventory of Bramble sharks Echinorhinus brucus (Bonnaterre, 1788) (Elasmobranchii, Echinorhinidae) in natural history collections worldwide for conservation status assessment

FIG. 6. — Echinorhinus brucus (Bonnaterre, 1788) in Austrian (Vienna) collections: A-C, NMW 3065 (Entry 3); D-G, NMW 50137 (Entry 4); H-J, NMW 85158 (Entry 5).

FIG. 15 in An inventory of Bramble sharks Echinorhinus brucus (Bonnaterre, 1788) (Elasmobranchii, Echinorhinidae) in natural history collections worldwide for conservation status assessment

FIG. 15. — Echinorhinus brucus (Bonnaterre, 1788) in German (Stuttgart, Berlin and Hamburg) collections: A, SMNS 16252 (Entry 48); B-D, ZMB 4536 (Entry 50); E, ZMB 12541 (Entries 51-52); F, G, ZMB 34908 (Entry 53); H, I, ZMB 34909 (Entry 54); J, ZMB 34910 (Entry 55); K, L, ZMH 26192 (Entry 57).

FIG. 4 in An inventory of Bramble sharks Echinorhinus brucus (Bonnaterre, 1788) (Elasmobranchii, Echinorhinidae) in natural history collections worldwide for conservation status assessment

FIG. 4. — Numbers of individual Bramble sharks Echinorhinus brucus (Bonnaterre, 1788) in natural history collections worldwide, dated and grouped per decade (this survey, n = 157): A, Global waters (the Atlantic Ocean); B, European waters, including the north-eastern Atlantic Ocean and the Mediterranean Sea; C, American waters, including the north-western and the south-western Atlantic Ocean; D, African waters, including the eastern and the south-eastern Atlantic Ocean.

FIG. 20 in An inventory of Bramble sharks Echinorhinus brucus (Bonnaterre, 1788) (Elasmobranchii, Echinorhinidae) in natural history collections worldwide for conservation status assessment

FIG. 20. — Echinorhinus brucus (Bonnaterre, 1788) in French (Nantes) collections (continuation): A-E, MHNN.Z.019419 (Entry 73).

Fig. 8 in Troubled giants: The updated conservation status of the coconut crab (Birgus latro)

Fig. 8. Birgus latro (Linnaeus, 1767) in its natural habitat on Christmas Island in the Indian Ocean. A, feeding on fruit trees; B, feeding on coconuts. Photographs by Max Orchard.

Fig. 7 in Troubled giants: The updated conservation status of the coconut crab (Birgus latro)

Fig. 7. Threats to Birgus latro (Linnaeus, 1767) while crossing roads during breeding season migrations on Christmas Island in the Indian Ocean. A, cannibalism by coconut crabs; B, crab and vehicle in close proximity; C, recording each road kill incident; D, warning to motorists. Photographs by Max Orchard.

Fig. 10 in Troubled giants: The updated conservation status of the coconut crab (Birgus latro)

Fig. 10. Conservation actions for Birgus latro (Linnaeus, 1767) in Okinawa and Kagoshima Prefectures, Japan. A, the location of Okinawa and Kagoshima Prefectures. The collection of coconut crabs is regulated by legal protective ordinances in the entire Kagoshima Prefecture. B, detail of Okinawa Prefecture showing the islands where the collection of coconut crabs is regulated by legal protective ordinances, shown in red ovals (Tarama Village, Miyakojima City, and Ishigaki City). Islands shown in black ovals (Yonaguni Village, Taketoni Town, and Okinawa Island and its associated islands) do not have protective ordinances for coconut crabs.

Fig. 5 in Troubled giants: The updated conservation status of the coconut crab (Birgus latro)

Fig. 5. Life stages of Birgus latro (Linnaeus, 1767) on Christmas Island in the Indian Ocean. A, juvenile crab with pleon inside small snail shell; B, juvenile with pleon inside larger shell of African giant snail (an introduced species); C, young subadult with hardened pleon that had recently cast off its snail shell. Photographs by Max Orchard.

Fig. 6 in Troubled giants: The updated conservation status of the coconut crab (Birgus latro)

Fig. 6. Birgus latro (Linnaeus, 1767) in its natural habitat on Christmas Island in the Indian Ocean. A, two adults mating; B, gravid female carrying eggs; C, female releasing eggs into the sea. Photographs by Max Orchard.

Fig. 9 in Troubled giants: The updated conservation status of the coconut crab (Birgus latro)

Fig. 9. Threats to Birgus latro (Linnaeus, 1767) on Christmas Island (Indian Ocean) from aggressive, invasive yellow crazy ants (Anoplolepis gracilipes). A, ants attacking the arthrodial membranes between peg articles; B, ants attacking the eyestalks; C, ants swarming on the body of a coconut crab. Photographs by Max Orchard. These images were kindly provided by Atara Film GmbH / NDR Doclights, from the film "Realm of the Robber Crab".

Fig. 4 in Troubled giants: The updated conservation status of the coconut crab (Birgus latro)

Fig. 4. Updated localities where Birgus latro (Linnaeus, 1767) is either extirpated (red, darkest circles) or its continued existence is uncertain (yellow, lightest circles). Note that the scale of the map may imply a wider area of extirpation than is actually known, so reference to the text and Table 3 is recommended to see the exact localities where extirpation is suspected.

Fig. 3 in New distribution records and conservation status of Atelopus seminiferus Cope, 1874: A Critically Endangered harlequin frog from northern Peru

Fig. 3. Updated distribution map of Atelopus seminiferus. Black dots indicate new localities reported in this study. Light green area corresponds the estimated Extent of Occurrence (ca. 2,520 km2) based on the new records presented here and the previously known localities. Numbers correspond to labels in Table 1. Map by Juan C. Cusi.

Fig. 3 in New distribution records and conservation status of Atelopus seminiferus Cope, 1874: A Critically Endangered harlequin frog from northern Peru

Fig. 3. Dorsal and ventral views of the holotype of Atelopus seminifeus (ANSP 11383), deposited in the herpetological collection at the Academy of Natural Sciences of Drexel University, Philadelphia. Photos courtesy of Ned Gilmore.

Fig. 2 in New distribution records and conservation status of Atelopus seminiferus Cope, 1874: A Critically Endangered harlequin frog from northern Peru

Fig. 2. (A) A pair of Atelopus seminiferus in amplexus, found between El Carmen and La Esperanza [not collected]. Photo by Fredi Sangama and Florencio León. (B) Dorsal coloration pattern of a female MUSM 33328. (C) Ventral coloration pattern in a male MUSM 33327. (D) Ventral coloration pattern in a female MUSM JCM H-24. (D) El Carmen village in Alto Mayo Protected Forest, Rioja province, San Martin (E). Photos B‒E by Juan C. Cusi.

Fig. 1 in New distribution records and conservation status of Atelopus seminiferus Cope, 1874: A Critically Endangered harlequin frog from northern Peru

Fig. 1. Distribution of Atelopus seminiferus in the Mayo River basin, San Martin, Peru. Yellow polygon corresponds to geographic range estimated by IUCN. Compare with Fig. 3, which shows proposed new polygon based on results from this study. Map by Juan C. Cusi.

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Fig. 2 in Climatic niche, natural history, and conservation status of the Porthole Treefrog, Charadrahyla taeniopus (Günther, 1901) (Anura: Hylidae) in Mexico

Fig. 2. Current (A), and future 2050 (B) and 2070 (C) scenarios of the climatic niche of Charadrahyla taeniopus in Sierra Madre Oriental province (degraded area). The color scale indicates the probability of occupancy for the species.

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Fig. 1 in Climatic niche, natural history, and conservation status of the Porthole Treefrog, Charadrahyla taeniopus (Günther, 1901) (Anura: Hylidae) in Mexico

Fig. 1. Female individual of Charadrahyla taeniopus (A) in a cloud forest and (B) at Tenango de Doria, Hidalgo, Mexico. Photos by Uriel Hernández-Salinas (A) and Raciel Cruz-Elizalde (B).