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FIG. 2 in Ecomorphological diversity in the Patagonian assemblage of bats from Argentina

FIG. 2. Skull variables measured in Patagonian bats from Argentina, shown on a H. macrotus specimen (LIEB-M 851 ♀). See text for abbreviations. Scale bar is 10 mm

FIG. 3 in Molecular dietary analysis of the endangered Ozark big-eared bat (Corynorhinus townsendii ingens)

FIG. 3. The occurrence of each moth family recovered through molecular identification of insect DNA recovered from 33 Ozark big-eared bat fecal pellets

FIG. 2 in Molecular dietary analysis of the endangered Ozark big-eared bat (Corynorhinus townsendii ingens)

FIG. 2. Results of molecular dietary analysis for Ozark big-eared bat (C. townsendii ingens) fecal pellets: A — number of times each prey species was detected among 33 guano pellets, B — number of prey species detected in each of the 33 guano pellets

FIG. 2 in A novel food preference in the greater short-nosed fruit bat, Cynopterus sphinx: mother-pup interaction a strategy for learning

FIG. 2. Behavioural responses of C. sphinx pups to the novel food during preference test. Pups feeding attempts (A), and feeding bouts (B) to the known and novel fruits, pups trained with mother showed more number of feeding attempts and bouts towards the novel fruits than other group pups. Data were shown as 0 ± SEM; *** — P <0.001

FIG. 1 in Swarming behaviour, catchment area and seasonal movement patterns of the Bechstein's bats: implications for conservation

FIG. 1. Map of the Belgium and adjacent countries (inset top right) indicating the location of study area. Within the study are (main figure), sampled swarming sites and recovered roost sites are indicated (grey pentagons and black circles, respectively). Forest fragments are shaded according to age (recent: light grey; ancient: dark grey). Capture site abbreviations correspond to those used in Table 1

FIG. 1 in Host-parasite relationships between a Malagasy fruit bat (Pteropodidae) and associated bat fly (Diptera: Nycteribiidae): seasonal variation of host body condition and the possible impact of parasite abundance

FIG. 1. Location map of the study site, Grotte des Chauves-souris, in the Parc National d'Ankarana, northern Madagascar

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FIG. 1 in What is for dinner? First report of human blood in the diet of the hairy-legged vampire bat Diphylla ecaudata

FIG. 1. Topology of Bayesian inference (SYM + gamma distribution) and maximum parsimony based on 260 bp of Cytb between sequences obtained from fecal samples of D. ecaudata in the Caatinga drylands of Northeastern Brazil and sequences of H. sapiens, G. gallus, and D. ecaudata originating from GenBank. The number above and below the branches indicate the statistic support for branches of posterior probabilities and bootstrap, respectively. Sequences from GenBank show their respective access codes

FIG. 5 in Species richness, functional diversity and assemblage structure of insectivorous bats along an elevational gradient in tropical West Africa

FIG. 5. Mean nearest taxon distances (MNTD) of multivariate traits (A and B), forearm length (C and D), greatest skull length (E and F), narrowest breadth of skull (G and H), ear length (I and J) and tail length (K and L) of insectivorous bats along the Mount Nimba elevational gradient. Observed MNTD for each elevation is represented by the green dots. A green line of best fit is shown for significant relationships between observed MNTD and elevation. The red dots indicate the expected MNTD as calculated by 999 randomized community shuffles for figures on the left, and trait shuffles for figures on the right. A red line of best fit is shown for significant relationships between expected MNTD and elevation. Instances where observed MNTD differs significantly from the expected MNTD are indicated by black rings

FIG. 1 in How do young bats find suitable swarming and hibernation sites? Assessing the plausibility of the maternal guidance hypothesis using genetic maternity assignment for two European bat species

FIG. 1. Left — drawing of 'Brunnen Meyer'; right — photo of the western side of the 'Brunnen Meyer' well house with window where bats enter

FIG. 5 in Spatial heterogeneity of fruit bats in a primary tropical lowland evergreen rainforest in northeastern Luzon, Philippines

FIG. 5. Wing loading and aspect ratio of eight fruit bat species captured in a primary tropical lowland evergreen rainforest in northeastern Luzon, Philippines. Mean values of each flight index are shown with 95% confidence intervals. Sample size for all species is n = 10 (five adult males and five non-pregnant adult females), except for E. spelaea (n = 5, all adult males)

FIG. 3 in Species richness, functional diversity and assemblage structure of insectivorous bats along an elevational gradient in tropical West Africa

FIG. 3. Dendrogram of bat functional groups present on Mount Nimba. Eight functional groups were identified, each represented by a different colour. See Supplementary Table S1 for full species names

FIG. 1 in Diet determined by next generation sequencing reveals pest consumption and opportunistic foraging by bats in macadamia orchards in South Africa

FIG. 1. Map of study area showing location of study area in South Africa and Limpopo Province (A) and detailed location of faecal pellet collection sites within the study area (B). Grey shading indicates the extent of vegetation types associated with the Soutpansberg Mts. Numbers represent localities as follows: 1) Farm Vlakfontein, 2–5) Farm Welgevonden, 6) Farm Laatsgevonden

FIG. 2 in Spatial heterogeneity of fruit bats in a primary tropical lowland evergreen rainforest in northeastern Luzon, Philippines

FIG. 2. Accumulation curves of species in (A) the understory and canopy, and in (B) ridges, streams, and forest edges in a primary tropical lowland evergreen rainforest in northeastern Luzon, Philippines. Curves are constructed based on averaging from random permutations of the weighted data

FIG. 1 in Spatial heterogeneity of fruit bats in a primary tropical lowland evergreen rainforest in northeastern Luzon, Philippines

FIG. 1. Location of the study area in the Northern Sierra Madre Natural Park, province of Isabela, northeastern Luzon, Philippines. Dark grey indicates forested areas, light grey indicates water bodies, and white indicates open areas. Map adapted from NAMRIA basemap downloaded from http://www.geoportal.gov.ph/viewer

FIG. 1 in Species richness, functional diversity and assemblage structure of insectivorous bats along an elevational gradient in tropical West Africa

FIG. 1. Study sites in Liberia and Guinea (Google Earth, 2015) and their assignment to the eight elevation belts. Key for site colours: red: <500 m; green: 500–600 m; yellow: 601–800 m; blue: 801–900 m; purple: 901–1100 m; black: 1101–1200 m; orange: 1201– 1400 m; white: 1401–1600 m

FIG. 4 in Spatial heterogeneity of fruit bats in a primary tropical lowland evergreen rainforest in northeastern Luzon, Philippines

FIG. 4. Capture rates of eight fruit bat species (A–H) in ridges, streams, and forest edges in a tropical lowland evergreen rainforest in northeastern Luzon, Philippines. Capture rates are expressed as the number of individuals captured per mist-net hour (m2·h). Bars indicate standard errors. Statistics refer to Kruskal-Wallis tests. Note the different y-axis scale for (C) E. robusta and (H) R. amplexicaudatus

Fig 5. A in The oldest known bat skeletons and their implications for Eocene chiropteran diversification

Fig 5. A composite stratigraphic column of the Green River Formation showing the relative position of the Fossil Butte Member and stratigraphic levels where various bat fossils have been found. The Fossil Butte Member is the thinnest of the members in the Green River Formation, but was deposited when the lake was deepest, providing conditions that were optimal for exceptional preservation. Five units in the Fossil Butte Member (Sandwich Beds, 18-inch Layer, Minifish Bed, Gastropod Beds, and Upper Split-fish Bed) are actively quarried on private and stateowned land by companies collecting the abundant fossil fish to sell. Among the fish, one bat is found on average every two years. To date, all bats have come from the 18-inch Layer and Sandwich Beds. Bat specimens are coded by color: Icaronycteris gunnelli in red, I. index in orange, Onychonycteris finneyi in blue, and unidentified or indeterminate are black. More than 10 bat specimens are held in private collections (not shown here), but none are confirmed lower in the section than the two specimens of I. gunnelli. Left two columns modified after Buchheim et al, 2011 [40]. https://doi.org/10.1371/journal.pone.0283505.g005

Fig 3 in The oldest known bat skeletons and their implications for Eocene chiropteran diversification

Fig 3. Skeleton of paratype of Icaronycteris gunnelli (ROM:Palaeobiology-Vertebrate Fossils:52666). https://doi.org/10.1371/journal.pone.0283505.g003

Fig 4 in The oldest known bat skeletons and their implications for Eocene chiropteran diversification

Fig 4. Remaining deposits of Fossil Lake sediments of the Green River Formation are illustrated in gray with highly-fossiliferous, deep-water, laminated limestone deposits of Eocene Fossil Lake in southwest Wyoming and poorly-fossiliferous, shallow-water, non-laminated limestones in northeast Utah and southeast Idaho. Eleven of more than 20 fossil quarries are still active today. Three active quarries (A, B and D) and one inactive quarry (C) have produced fossil bats currently held in public institutions. All other historic and active quarry locations are marked by small black dots. American Fossil Quarry (A) yielded I. gunnelli (AMNH.FM.145747 and ROM.52666), I. index (AMNH.FM.125000 and AMNH.FM.144215), I. cf index (WDC-CGR-115) and O. finneyi (AMNH.FM.142467 and ROM.55351). Thompson Ranch north quarry (B) yielded I. index (FMNH.PM.62096 and HMNS.PV.001468). The Holland brother's quarry (C) was active for only one season in the mid-1930s and yielded I. index (YPM-PU.18150). The Smith Hollow quarry (D) yielded a poorly preserved and unidentified specimen (FOBU13777). Most bat specimens were recovered from two quarries operating continuously since the 1980s in nearshore deposits. A combination of proximity to the eastern shore and a large volume of rock excavated is the most probable explanation for the greater number of bat fossils being discovered in those locations. https://doi.org/10.1371/journal.pone.0283505.g004

Fig 2 in The oldest known bat skeletons and their implications for Eocene chiropteran diversification

Fig 2. Illustrated dentitions of Green River bats. A) Onychonycteris finneyi (ROM 55351A-B) upper P1-M3; B) Icaronycteris index (YPM-PU 18150) upper P1-M3; C) Icaronycteris gunnelli (FM.145747A) upper P1-M3; D) Icaronycteris gunnelli (FM.145747A) lower c1-m3, with reconstructed i1-i3, in labial view. Abbreviations of features discussed in the text: dc—distal cingulid; ec—ectocingulum; ef—ectoflexus; hs—hypocone shelf; lc—lingual cingulum; pbc—posterobasal cusp; prm—premetacrista; prp—preparacrista; ps—parastyle; psm—postmetacrista; psp— postparacrista; tal—talonid. https://doi.org/10.1371/journal.pone.0283505.g002