Find research datasets worth reusing

Fig. 1 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 1. (c) one subtree in the Arabian Gulf/South Africa clade showing two clusters: the South Africa clade and the Western Arabian Gulf type (WA) clade; (d) subtree in the Arabian Gulf/South Africa clade showing one group that is identical to the West Indian Ocean II (WIO II) group from Lo et al. (2017), WIO II type A, and WIO II type B. The black numbers at nodes are bootstrap supporting values (%). Only values larger than 80% are shown. Grey numbers in italics on the branches represent branch length, with only those longer than 3% plotted. Samples collected from the Arabian Gulf are abbreviated with LKR.

Fig. 1 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 1. Male Austruca variegata (Heller, 1862) (a–d) and Cranuca inversa (Hoffmann, 1874) (e). (a) habitus; (b, c) major cheliped; (d, e) merus of right major cheliped. (a, b) lectotype, CW 17.2 mm (PL 24.7 mm, NHMW 25656; Madras, India), originally identified as A. perplexa. (c) "Gelasimus perplexus" in Heller (1865: pl. 5(4)). (d) male (CW 18.6 mm, ZRC 2018.1375; Tamil Nadu, India). (e) CW 19.9 mm (NCHUZOOL 14904; Al Darb, Arabia). Scale bars = 5.0 mm.

Fig. 6. Right G1s in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 6. Right G1s of Austruca variegata (Heller, 1862) (a, b, c, f), A. bengali (Crane, 1975) (d, g) and A. triangularis (A. Milne-Edwards, 1873) (e, h). (a, f–h) lateral view of distal part; (b) mesial view of distal part; (c–e) lateral view. (a, b) CW 16.6 mm (ZRC 2001.0853; Tamil Nadu, India); (c, f) CW CW 14.5 mm (ZRC 2017.0917; West Bengal, India); (d, g) 14.5 mm (NCHUZOOL 14345; Selangor, Malaysia); (e, h) 14.8 mm (NCHUZOOL 13574; Cebu, Philippines). Scale bars: a, b, f–h = 0.5 mm, c–e = 1.0 mm.

Fig. 7 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 7. The first gill arch (left panels, scale bar = 10 mm) and swim bladder (right panels, scale bar = 50 mm) for the WIO IIA, WIO IIB groups, and Otolithes arabicus sp. nov.

Fig. 10 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 10. The live coloration of Austruca bengali (Crane, 1975) (a–g). (a, b) dorsal view of adult male; (c, d) dorsal view of juvenile male; (e) frontal view of adult male; (f) frontal view of juvenile female; (g) a female in the field (not captured; Phuket, Thailand); (h) habitat in Phuket, Thailand. (a) male (not captured; Selangor, Malaysia); (b) male (not captured; Phuket, Thailand); (c, d) male (CW 7.3, 7.8 mm, NCHUZOOL 14361; Phuket, Thailand); (e) male (CW 14.5 mm, NCHUZOOL 14345; Selangor, Malaysia); (f) female (CW 8.1 cm, NCHUZOOL 14361; Phuket, Thailand).

Fig. 5 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 5. Outer and inner sides of major palm of Austruca variegata (Heller, 1862) (a–d), A. bengali (Crane, 1975) (e, f) and A. triangularis (A. MilneEdwards, 1873) (g, h). (a, b) CW 16.6 mm (ZRC 2001.0853; left-handed; Tamil Nadu, India); (c, d) CW 14.5 mm (ZRC 2017.0917; left-handed; West Bengal, India); (e, f) CW 14.5 mm (NCHUZOOL 14345; right-handed; Selangor, Malaysia); (g, h) CW 14.8 mm (NCHUZOOL 13574; lefthanded; Cebu, Philippines).

Fig. 9 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 9. The live coloration of Austruca variegata (Heller, 1862) (a–h). (a, b) dorsal view of male; (c, d) frontal view of male; (e) dorsal view of female; (f) two males fighting; (g) two males moving to low intertidal zone for feeding; (h) a male A. variegata (left) and a male A. annulipes (H. Milne Edwards, 1837) (right) sympatric in one locality. Specimens not captured. Photos taken from Vellar River estuary, Porto Novo, Tamil Nadu, India.

Fig. 3 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 3. (a) Canonical analysis of principal coordinates for 30 standardized morphology measurements based on Euclidean distance. Letters A, B, and WA indicate the mean canonical value of the WIO IIA, WIO IIB, and WA groups, respectively. Error bars around the mean present one standard error. (b) Contributions of different measurements (measurement scores, proportional to the eigenvalues) on the constrained ordination plot. The measurement abbreviations refer to appendix 1.

Fig. 1 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 1. (a) Full phylogenetic tree of the genus Otolithes with specimens from the Indo-Pacific, Western Arabian Gulf, and South Africa by Kimura- 2P distance and maximum-likelihood distance using the GTR + G nucleotide substitution model and Protonibea diacanthus as the outgroup; (b) subtree showing three clades: the Otolithes cuvieri complex, the Otolithes ruber Western Indo Pacific clade, and the Otolithes sp. Arabian Gulf/South Africa clade. The black numbers at nodes are bootstrap supporting values (%). Only values larger than 80% are shown. Grey numbers in italics on the branches represent branch length, with only those longer than 3% plotted.

Fig. 6 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 6. Fresh specimen of the holotype of Otolithes arabicus sp. nov. The scale bar represents 5 cm, and each block represents 1 cm.

Fig. 3 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 3. Asymptotic analysis of the diversity (Hill numbers, q = 0, 1 and 2) of phyllostomid bats in neotropical temperate forests (MCF: montane cloud forest, POF: pine-oak forest) and agricultural areas (AGR) in southern Mexico. Shadded areas are confidence intervals at 0.95%.

Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 4. (a) Illustration of 17 landmarks on the Otolithes sp. 1: tip of snout, 2: termination of maxilla, 3: ventral margin of interopercle, 4: anterior margin of eye orbit, 5: posterior margin of eye orbit, 6: dorsal termination of cranium, 7: origin of lateral line, 8: origin of pectoral fin, 9: origin of pelvic fin, 10: anterior insertion of spinous dorsal fin, 11: origin of soft dorsal fin, 12: origin of anal fin; 13: termination of anal fin, 14: termination of second dorsal fin, 15: insertion of dorsal-most caudal fin ray, 16: termination of lateral line, and 17: insertion of ventral-most caudal fin ray. Procrustes superimposition showing the pair-wise differences in shapes between (b) Western Arabian Gulf group (WA) vs. West Indian Ocean II group, and (c) West Indian Ocean II group type A vs. B. Arrows indicate the difference vector, which is amplified four times for clarity.

Fig. 4 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 4. Floors of orbit of male Austruca variegata (Heller, 1862) (a–d), A. bengali (Crane, 1975) (e, f) and A. triangularis (A. Milne-Edwards, 1873) (g, h). (a, b) CW 18.6 mm (ZRC 2018.1375; right-handed; Tamil Nadu, India); (c, d) CW 14.5 mm (ZRC 2017.0917; left-handed; West Bengal, India); (e, f) CW 14.5 mm (NCHUZOOL 14345; right-handed; Selangor, Malaysia); (g, h) CW 14.8 mm (NCHUZOOL 13574; left-handed; Cebu, Philippines). Scale bars = 5.0 mm.

opencc-by-4.0Sep 2021View details →

Figures 5-8 in Apu, a new genus of Euchromiina (Lepidoptera: Erebidae: Arctiinae: Arctiini), and a new species from the montane forests of southeastern Peru

Figures 5-8. Male genitalia of Apu mooreorum sp. nov. (Genitalia # JGA-411, MUSM). 5-7. 5. Vista dorsal. 6. Vista ventral. 7. Vista lateral. 8. Aedeagus. Scale: 1 mm. / Genitalia macho de Apu mooreorum sp. nov. (Genitalia # JGA-411, MUSM). 5-7. 5. Vista dorsal. 6. Vista ventral. 7. Vista lateral. 8. Edeago. Escala: 1 mm.

opencc-by-4.0Sep 2021View details →

Figures 11-12 in Apu, a new genus of Euchromiina (Lepidoptera: Erebidae: Arctiinae: Arctiini), and a new species from the montane forests of southeastern Peru

Figures 11-12. Apu flavicornis (Druce, 1893) comb. nov. Syntype female in NHMUK. 11-12. 11. Dorsal view. 12. Ventral view. / Apu flavicornis (Druce, 1893) comb. nov. Sintipo hembra en NHMUK. 11-12. 11. Vista dorsal. 12. Vista ventral.

opencc-by-4.0Sep 2021View details →

Figures 9-10 in Apu, a new genus of Euchromiina (Lepidoptera: Erebidae: Arctiinae: Arctiini), and a new species from the montane forests of southeastern Peru

Figures 9-10. Apu flavicornis (Druce, 1893) comb. nov. (Nieva river). 9-10. 9. Vista dorsal. 10. Vista ventral. Scale: 5 mm. / Apu flavicornis (Druce, 1893) comb. nov. (rÍo Nieva). 9-10. 9. Vista dorsal. 10. Vista ventral. Escala: 5 mm.

Fig. 5 in Value of forest remnants for montane amphibians on the livestock grazed Mount Mbam, Cameroon

Fig. 5. Non-metric dimensional scaling plot of amphibian community structure divided by land use type on Mount Mbam based on visual encounter surveys with equal effort for each land use. The PERMANOVA p-value is shown in the top right corner.

Fig. 4 in Value of forest remnants for montane amphibians on the livestock grazed Mount Mbam, Cameroon

Fig. 4. Montane endemic amphibian species observed in recent surveys of Mount Mbam, West-Region, Cameroon. a) Astylosternus rheophilus, b) Astylosternus montanus, c) Afrixalus aff. fulvovittatus, d) Hyperolius balfouri, e) Hyperolius igbettensis, f) Hyperolius nitidulus, g) Hyperolius concolor, h) Hyperolius cinnamomeoventris, i) Hyperolius tuberculatus, j) Leptopelis nordequatorialis, k) Leptopelis boulengeri, l) Phrynobatrachus steindachneri, m) Xenopus cf. eysoole, n) Hoplobatrachus occipitalis, and o) Sclerophrys maculata.

Fig. 2 in Value of forest remnants for montane amphibians on the livestock grazed Mount Mbam, Cameroon

Fig. 2. Montane habitats of amphibian species observed in recent surveys of Mount Mbam, West-Region, Cameroon: a) gallery forest during the rainy season; b): gallery forest during the dry season after a bushfire; c) savanna area transformed by overgrazing; and d): effects of bushfire started for pasture on the same site during the dry season.

Fig. 1 in Value of forest remnants for montane amphibians on the livestock grazed Mount Mbam, Cameroon

Fig. 1. Maps showing (top) the topography of the Bamenda Highlands, white circle showing Mount Mbam in the West Region of Cameroon; and (bottom) the layout of sample sites on Mount Mbam.