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152 results for “phyllostomid bats”
Fig. 5. Phyllostomid bat Macrotus waterhousii Gray, 1843 in Carnassiform notches improve the functional efficiency of bat molar shearing crests
Fig. 5. Phyllostomid bat Macrotus waterhousii Gray, 1843 (OMNH 10653) from Mexico, Recent. Lower molars showing carnassiform notches in the cristid obliqua (arrows) and postcristid and accompanying accessory troughs in the talonid basins of m1–m2, in anterolabial view (A1) and occlusal (A2, stereopair) views, notches indicated by arrows. Chrotopterus auritus show carnassiform notches similar to those on the trigonid crests of many insectivorous bats. However, these specialized carnivorous bats lack notches in the talonid crests. CN and accessory troughs are moderately developed in Macrotinae (Macrotus; Fig. 5) and most strongly expressed in Micronycterinae (Micronycteris and Lampronycteris; Fig. 6), Lonchorhininae (Lonchorhina; Fig. 7), Phyllostomini (Gardnerycteris, Lophostoma, Phylloderma, Phyllostomus, and Tonatia; Fig. 8), and Glyphonycterinae (Glyphonycteris, Neonycteris, and Trinycteris; Fig. 9). Regarding the micronycterines, Micronycteris has been shown to exhibit a high degree of dietary flexibility; Santana et al. (2011a) showed that Micronycteris microtis, a small (5–7 g) species, ate a wide variety of insects, spiders, and a tiny lizard making them the smallest bat known to exhibit rare carnivory. Much of the species' feeding behavior involved chewing motions involving the premolars and molars. Based on molecular evidence, Glyphonycterinae was recently recognized as a distinct subfamily of Phyllostomidae within a radiation of omnivorous and frugivorous bats (the Nullicauda, including Carolliinae, Glyphonycterinae, Rhinophyllinae, and Stenodermatinae; Cirranello et al. 2016), and contains the genera Glyphonycteris, Neonycteris, and
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.
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.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
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