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Figure 3 in Systematic analysis of leisler's bat Nyctalus leisleri (Kuhl, 1817) captured from FATA region, Pakistan

Figure 3. Genus Nyctalus peculiar to COI by Neighbour Joining method. Number shows percent of 1000 bootstraps replication above 50. ♦ shows the sequences of species of the present research.

Fig. 2 in Bats of Sicily: historical evidence, current knowledge, research biases and trends

Fig. 2 - Documents in the primary and secondary datasets and the cumulative number of documents issued between 1810 and 2022. / Documenti nei dataset primario e secondario e numero cumulativo di documenti prodotti tra il 1810 e il 2022.

Fig. 5 in Bats of Sicily: historical evidence, current knowledge, research biases and trends

Fig. 5 - Distribution of the primary dataset, secondary dataset, and total documents according to research areas and used methods. / Distribuzione del dataset primario, del dataset secondario e del totale dei documenti in base alle aree di ricerca e ai metodi utilizzati.

Fig. 1 in Bats of Sicily: historical evidence, current knowledge, research biases and trends

Fig. 1 - Flow diagram showing the selection steps of eligible documents obtained from primary and secondary datasets. / Diagramma di flusso che mostra le fasi di selezione dei documenti eligibili ottenuti dai dataset primario e secondario.

Fig. 4 in Bats of Sicily: historical evidence, current knowledge, research biases and trends

Fig. 4 - (A) Bar plot showing the distribution of studies across different habitats (caves, forest, urban area, riparian areas). (B) Species conservation status across Sicilian bat families classified according to the IUCN categories: Least Concern (LC), Vulnerable (VU), Near Threatened (NT), and Data Deficient (DD). / (A) Grafico a barre che mostra la distribuzione degli studi nei diversi habitat (grotte, foreste, aree urbane, aree ripariali). (B) Stato di conservazione delle specie delle famiglie di pipistrelli siciliani classificate secondo le categorie IUCN: Minima preoccupazione (LC), Vulnerabile (VU), Quasi minacciata (NT) e Carenza di dati (DD).

Fig. 3 in Bats of Sicily: historical evidence, current knowledge, research biases and trends

Fig. 3 - Variation of Bat Research Efficiency scores (BRE) in the nine Sicilian provinces. The colour gradient (darker to lighter) indicates a higher to lower BRE. / Variazione dei punteggi di efficienza della ricerca sui pipistrelli (BRE) nelle nove province siciliane. Il gradiente di colore (da più scuro a più chiaro) indica un BRE da più alto a più basso.

Fig. 4 in The relationships among Leishmania infantum and phyllostomid bats assessed by histopathological and molecular assays

Fig. 4. Photomicrography of spleen of an adult male Artibeus planirostris (A) and Carollia perspicillata (B) qPCR Leishmania infantum positive. No amastigotes forms were found. Note tingible bodies macrophages in the germinal center containing phagocytic apoptotic cells (arrow) and apoptotic cells (arrowhead), H&E, 40x objective.

Fig. 2 in The relationships among Leishmania infantum and phyllostomid bats assessed by histopathological and molecular assays

Fig. 2. Photomicrography of liver of an adult female Leishmania infantum negative Carollia perspicillata presenting cytoplasmic vacuolation of hepatocytes (arrowhead) and mild lymphocytic infiltrate of portal area (arrow), H&E, 40x objective.

Fig. 3 in The relationships among Leishmania infantum and phyllostomid bats assessed by histopathological and molecular assays

Fig. 3. Photomicrography of spleen of an adult male Artibeus planirostris qPCR Leishmania infantum positive. No amastigotes forms were found, only unspecific mild hyperplasia (big ellipse) and hypoplasia (small ellipse) of lymphoid follicles in the reactive white pulp. Note the lack of delimitation between the WP and red pulp (RP), H&E, 10x objective. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in The relationships among Leishmania infantum and phyllostomid bats assessed by histopathological and molecular assays

Fig. 1. Photomicrography of wing skin of an adult male Artibeus planirostris qPCR Leishmania infantum positive. No amastigotes forms were found, only unspecific mild mixed inflammatory infiltrate of dermis with mononuclear (arrow) and polymorphonuclear cells (arrowhead), H&E, 40x objective.

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.