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Figs 25–27 in Oribatid Mites (Acari: Oribatida) From Venezuela, Ii. New Or Rare Species From Montane Forests

Figs 25–27. Rostrozetes (Rostrozetella) decorus sp. n.: 25 = body in dorsal view, 26 = body in ventral view, 27 = lateral part of the podosoma in lateral view

Figs 15–22 in Oribatid Mites (Acari: Oribatida) From Venezuela, Ii. New Or Rare Species From Montane Forests

Figs 15–22. Distinguishing characters of Acrozetes species. 15–18 = Arcozetes rotundatus sp. n.: 15 = body in dorsal view, 16 = rostral part of the podosoma in lateral view, 17 = prodorsum in dorsal view, 18 = sensillus. 19–21 = Arcozetes bicuspidatus HAMMER, 1958: 19 = sensillus, 20 = prodorsum in

Figs 6–9 in Oribatid Mites (Acari: Oribatida) From Venezuela, Ii. New Or Rare Species From Montane Forests

Figs 6–9. Beckiella disiuncta sp. n. 6 = body in dorsal view, 7 = body in ventral view, 8 = humeral part of the notogaster, 9 = leg IV

Figs 10–14 in Oribatid Mites (Acari: Oribatida) From Venezuela, Ii. New Or Rare Species From Montane Forests

Figs 10–14. Sternoppia pocsiana sp. n.: 10 = body in dorsal view, 11 = rostral apex in frontal view, 12 = body in ventral view, 13 = lateral part of the podosoma in lateral view, 14 = lateral view of the body

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

Fig. 4. Unidentified taxa. Blenniidae sp. 1 (a); Blenniidae sp. 2 (b); Coilia sp. 1 (c); Callionymidae sp. 1 (d); Sillaginidae sp. 1 (e); Soleidae sp. 1 (f); Platycephalidae sp. 1 (g).

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

Fig. 3. Three degrees of pigmentation on the top of head of A. gymnocephalus larvae; heavy pigment (a); moderate pigment (b); sparse pigment (c, d).

Fig. 1 in Fig. 3 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 1. Map of sampling location (left) and enlarged inset box (right) showing five sampling stations (black circles) along the Klang Strait. Right arrow indicates offshore direction of transect line from Kapar power plant.

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

Fig. 2. Ontogenetic series of E. thoracata at preflexion (a); flexion (b, c); postflexion (d, e); early juvenile (f).

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

Fig. 4. Unidentified taxa. Trypauchen sp. 1 (h); Gobiidae sp. 1 (i); Gobiidae sp. 2 (j); Gobiidae sp. 3 (k); Gobiidae sp. 4 (l); Gobiidae sp. 5 (m); Gobiidae sp. 6 (n); Gobiidae sp. 7-1 (o); Gobiidae sp. 7-2 (p); Gobiidae sp. 8 (q).

Fig. 4 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. 4. Five developmental stages of feathers and the regulators for natal down growth suppression in zebra finch. (A) Schematic diagram shows the five developmental stages of feathers: LoGZ, invagination, branching, feather β-keratin, and dermal papilla (Wu et al. 2018). (B) A summary of the mRNAs identified in Type I and Type II feather formations in zebra finch (Chen et al. 2016).

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. 3 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. 3. The morphology of left chela of types of Parasesarma liho (A–B), P. cognatum (C–D) and P. paucitorum (E–H). A, C, E, G, outer view; B, D, F, H, upper view. A, B, holotype of P. liho (CW 13.0 mm, SMF 36266); C, D, holotype of P. cognatum (CW 14.3 mm, NMMBCD 3975); E, F, paratype of P. paucitorum (CW 15.5 mm, ZRC 2019.0578); G, H, holotype of P. paucitorum (CW 19.7 mm, MZB Cru 2243). Scales bars = 2 mm.

Fig. 5 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. 5. The coloration of Parasesarma liho in the field in Taiwan. A, specimen (not captured) from Gangkou R. estuary, Pingtung; B, specimen (not captured) from Meilun R. estuary, Hualien.

Fig. 2 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. 2. The morphological variation of distal part the right G1s of Parasesarma liho (A–H), and P. paucitorum (I). A, CW 11.1 mm (NCHUZOOL 15022), Pingtung, Taiwan; B, CW 11.6 mm (NCHUZOOL 15027), Hualien, Taiwan; C, CW 12.7 mm (ZSM A20100040, paratype of P. liho), Hualien, Taiwan; D, CW 13.29 mm (NCHUZOOL 15034), Cebu, Philippines; E, CW 14.3 mm (NMMBCD 3975, holotype of P. cognatum), Pingtung, Taiwan; F, CW 15.5 mm (ZRC 2019.0578, paratype of P. paucitorum), Sulawesi, Indonesia; G, CW 16.2 mm (NCHUZOOL 15022), Pingtung, Taiwan; H, CW 16.7 mm (NCHUZOOL 15031), Pingtung, Taiwan; I, CW 19.7 mm (MZB Cru 2243, holotype of P. paucitorum), Sulawesi, Indonesia. Scales bars = 0.5 mm.

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. Relationship between species abundance and climatic predictors according to the generalized linear models. Solid lines represent the fitted values (prediction) of the models, and the shaded area shows the 95% confidence interval of the predicted values of each model. Colour-code points indicate data by precipitation season (low and high).

Fig. 1 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. 1. Schematic drawing showing the measurement of the length, as well as the maximum and minimum widths of the propodi of the fourth pereiopods (third ambulatory leg, P4) used in this study.

Fig. 3 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. 3. Schematic diagram of bird hatchlings. Dorsal (upper row) and ventral (lower row) views of chicken (precocial), pigeon (semialtricial), parrot (altricial) and zebra finch.

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. Geographic location of the study area in relation to South America (A), Venezuela (B), Mérida State (C), and the Monte Zerpa Cloud Forest (D). Points indicate sampled areas.

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. Seasonal climatic and anuran variation among sampling sessions. (A) Principal Component Analysis (PCA) for all individual climate variables measured in 24 sampling sessions. The analysis included precipitation (Pp), relative humidity (RH) and air temperature (Temp). The level of Pearson correlation of each vector is indicated (cos2). (B) Principal Coordinate Analysis (PCoA) for the anuran assemblage based on species composition and abundance during the high and low precipitation seasons. The centroid points represent the average precipitation each month.

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. Anuran species recorded in the Monte Zerpa Cloud Forest. Hyalinobatrachium duranti (A), Hyloscirtus platydactylus (B), Hyloscirtus jahni (C), and Pristimantis vanadisae (D). Photos: Francisco Nava (A, C, D) and Pascual Soriano (B).