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Fig. 2 in Fig. 3 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 2. Schematic diagram of feather tract and types of natal down formation in zebra finch and chicken. Zebra finch embryos show two types of feather formation: Type I feather formation (open circles), in which the feather buds do not develop into downy feather; Type II feather formation (black circles), in which the feather buds develop into downy feathers, which are later replaced by contour feathers. Chicken embryos exhibit only the Type II feather formation. E8, E9, and E12: embryo day 8, 9 and 12, respectively. D7: 7 days post-hatch. Scale bar = 0.1 cm. The figure was modified from our previous study (Chen et al. 2017).

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. Abundance variation of anurans in the Monte Zerpa Cloud Forest. Differences in overall abundances among species (A), total anuran abundance between precipitation seasons (B), abundances by species between seasons (C) are presented. Letters indicate significant differences among groups according to post hoc tests (p <0.05), while ns indicates non-significant differences between samples.

Fig. 7 in Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 7. Genealogical network for the COI haplotypes observed within the clades of Parasesarma liho and other related species. Unlabelled hatches indicate inferred haplotypes not found in the sampled population. For haplotype names, see table 1.

Fig. 1. The modified time calibrated Bayesian tree and a in Fig. 3 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 1. The modified time calibrated Bayesian tree and a plot of four major avian developmental modes (Prum et al. 2015). The complete tree is divided into parts A and B. Scale in the Y-axis: millions of years ago.

Fig. 4 in Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 4. The outer surface of chelipedal meri of Parasesarma cognatum (holotype, NMMBCD 3975). A, left cheliped; B, right cheliped. Arrow indicates a subdistal angle on the upper margin of chelipedal merus.

Fig. 6. A in Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 6. A Bayesian inference (BI) tree of Parasesarma liho, as well as the outgroups, based on the cytochrome oxidase subunit I genes (COI). Probability values at the nodes represent support values for BI and maximum likelihood (ML). For haplotype names, see table 1.

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

Fig. 3. The relationship between nesting CCL (curved carapace lenght) size and latitude in marine turtles across different regions.

Fig. 2 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 2. The temporal change in the CCL (curved carapace length) and CCW (curved carapace width) values over the years (Black lines are Theil-Sen trend lines).

Fig. 12. A in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 12. A Bayesian inference tree of the Austruca variegata complex, with the outgroups of other congeneric species, based on the combined 28S, 16S and COI markers. Values at the nodes are Bayesian posterior probabilities.

Fig. 13 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 13. Genealogical network for the COI haplotypes observed within the clades of Austruca variegata (Heller, 1862), A. bengali (Crane, 1975) and A. triangularis (A. Milne-Edwards, 1873). Unlabelled hatches indicate inferred haplotypes not found in the sampled population. For haplotype names, see table 1.

Fig. 2 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 2. Austruca variegata (Heller, 1862). a–d, male (CW 18.6 mm, CL 10.7 mm, PL 26.6 mm, ZRC 2018.1375). (a) habitus; (b) major cheliped; (c) pleon; (d) minor cheliped. Scale bar = 5.0 mm.

Fig. 8 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 8. Female Austruca variegata (Heller, 1862) (a–d), A. bengali (Crane, 1975) (e) and A. triangularis (A. Milne-Edwards, 1873) (f). (a) habitus; (b) floor of right orbit; (c) right minor cheliped; (d–f) right vulva (gonopore). (a–d) CW 16.6 mm (NCHUZOOL 14365; Tamil Nadu, India); (e) CW 12.4 mm (QM W27320; Phuket, Thailand); (f) CW 14.6 mm (NCHUZOOL 14350; Cebu, Philippines). Scale bars: b, c = 5.0 mm, d–f = 0.5 mm

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

Fig. 3. Carapaces of male Austruca variegata (Heller, 1862) (a, b), A. bengali (Crane, 1975) (c) and A. triangularis (A. Milne-Edwards, 1873) (d). (a) CW 16.6 mm (ZRC 2001.0853; left-handed; Tamil Nadu, India); (b) CW 14.5 mm (ZRC 2017.0917; left-handed; West Bengal, India); (c) CW 14.5 mm (NCHUZOOL 14345; right-handed; Selangor, Malaysia); (d) CW 14.8 mm (NCHUZOOL 13574; lefthanded; Cebu, Philippines).

Fig. 2. Fresh specimen photos for West Indian Ocean II Group type A in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 2. Fresh specimen photos for West Indian Ocean II Group type A (WIO IIA) and West Indian Ocean II Group type B (WIO IIB), and western Arabian type (WA), and the posterior part of the soft dorsal fin. Scale bar = 5 cm.

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

Fig. 5. (a) The lateral face of the left sagittal otolith, from the WIO IIA, WIO IIB, and WA groups with a scale bar of 2 mm. (b) Canonical analysis of principal coordinates on the wavelet coefficients from otolith outlines based on Euclidean distance. Letters A, B, and WA indicate the mean canonical score of the WIO IIA, WIO IIB, and WA groups, respectively. Error bars around the mean present one standard error. (c) Mean otolith shape based on wavelet reconstruction for the WIO IIA, WIO IIB, and WA groups, respectively.

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

Fig. 7. Urocardiac ossicles of Austruca variegata (Heller, 1862) (a, b, e), A. bengali (Crane, 1975) (c, f) and A. triangularis (A. Milne-Edwards, 1873) (d, g). (a) male (CW 16.1 mm, ZRC 2003.0463; Tamil Nadu, India); (b, e) female (CW 14.5 mm, ZRC 2003.0463; Tamil Nadu, India); (c) male (CW 13.1 mm, QM W27320; Phuket, Thailand); (d) male (CW 14.8 mm, NCHUZOOL 13574; Cebu, Philippines); (f) male (CW 12.5 mm, QM W27320; Phuket, Thailand); (g) female (CW 14.6 mm, NCHUZOOL 14350; Cebu, Philippines). Scale bars = 0.5 mm.

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

Fig. 1. Location of sampling localities (white dots; two sampling sites per locality) for phyllostomid bats in Oaxaca, Mexico. Cover types: agricultural areas (AGR), pine-oak forest (POF), and montane cloud forest (MCF). Source: Google Earth (February 2012), Digital Globe and NASA.

Fig. 2 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 2. Rank abundance curves of phyllostomids bats in neotropical temperate forest and agricultural areas in southern Mexico.

Fig. 11 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 11. The live coloration of Austruca triangularis (A. Milne-Edwards, 1873). (a–d) dorsal view of adult male; (e, f) dorsal view of juvenile male; (g, h) frontal view of adult male. (a, g) NCHUZOOL 14347 (140716, Bali, Indonesia); (b, h) male (CW 11.5 mm, NCHUZOOL 14349; Cebu, Philippines); (c, d) specimens lost (Baoli River estuary, Pingtung, Taiwan); (f) NCHUZOOL 14346 (Labuan, Malaysia).

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

Fig. 4. Non-metric multidimensional scaling analysis (NMDS) ordination of phyllostomid bats in neotropical temperate forests and agricultural areas in southern Mexico. a) species composition, b) guilds. Cover types: agriculture (solid line), montane cloud forest (dashed line), and pine-oak forest (dotted line).