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Figure 3 in Observations of a greater sac-winged bat pup (Saccopteryx bilineata) with a chromatic disorder

Figure 3: The female pup of Saccopteryx bilineata with chromatic disorder (A). Both wing membranes, the tail membrane, and the skin showed normal colouration (B) whereas the fur was entirely white. However, some of the white hairs had black tips (C). Photo credit: S. Ripperger.

Figure 2 in Observations of a greater sac-winged bat pup (Saccopteryx bilineata) with a chromatic disorder

Figure 2: Entire isolation call from the leucistic pup. The multisyllabic call is composed of three different syllable types: (vs) variable simple syllables, end syllables which include the composite syllable type (cs) and the short stereotyped syllable type (ss). The composite syllable type is composed of two parts, a noisy part which is facultative (nc), connected to a tonal part (tc). The spectrogram depicts frequency (kHz) as a function of time and was generated using a 1042 point-fast Fourier transform with a Hamming window with 50 % overlap. Above the spectrogram, the oscillogram is depicted, displaying time on the x-axis and amplitude on the y-axis. Nomenclature follows (Fernandez and KnÖrnschild 2017).

Figure 1 in A multidisciplinary approach unveils the distribution of the Alpine long-eared bat Plecotus macrobullaris (Vespertilionidae) in Italy

Figure 1: Summary of the distribution of the Alpine long-eared bat in Italy. Colour coding: yellow, non-genotyped (scientific and grey literature); orange, non-genotyped (new occurrences); purple, genotyped.

Figure 1 in Potential seed dispersal of cumbaru (Dipteryx alata) by fruit-eating bats (Artibeus sp.) in a Brazilian urban context

Figure 1: Location of the bat roost (yellow point) monitored, in the urban area (blue circle) of the municipality of Cáceres, Central-Southern region of Mato Grosso state, Brazil.

Figure 2 in Potential seed dispersal of cumbaru (Dipteryx alata) by fruit-eating bats (Artibeus sp.) in a Brazilian urban context

Figure 2: Potential seed dispersal of Dipteryx alata by Artibeus sp. (A) Cerrado riparian forest located in an urban area of the municipality of Cáceres,Mato Grosso (Brazil) where potentially cumbaru tree (D. alata) is present, (B) roosting site used by two individuals of Artibeus sp. monitored for 21 consecutive days to quantify cumbaru frugivory and seed dispersal (C and D).

Figure 4 in Bats (Mammalia: Chiroptera) from two priority areas for biodiversity conservation in the Brazilian Amazon and range extension for Carollia benkeithi (Phyllostomidae)

Figure 4: Female specimen of Micronycteris sp. (MPEG 37789) registered in the Mamirauá SDR. (A) Dorsal (left) and ventral (right) fur views; (B) two upper dorsal views of the head showing the separation of the ear band (arrows). Scale bars: 10 mm.

Figure 1 in Bats (Mammalia: Chiroptera) from two priority areas for biodiversity conservation in the Brazilian Amazon and range extension for Carollia benkeithi (Phyllostomidae)

Figure 1: Map of South America showing the Mamirauá and Amanã Sustainable Development Reserves in Amazonas state, Brazil.

Figure 10 in On the systematic position of the horseshoe bats (Mammalia: Chiroptera) from Lesotho

Figure 10: Portrait and a frontal (middle) and lateral views (right) of the horseshoe of Rhinolophus cervenyi sp. n. (photo by J. Červený).

Figure 9 in On the systematic position of the horseshoe bats (Mammalia: Chiroptera) from Lesotho

Figure 9: Type locality of Rhinolophus cervenyi sp. n.: small cave near the old park lodge in the Sehlabathebe National Park, Lesotho, and the bat colony containing the type series (photo by J. Červený).

Figure 6 in On the systematic position of the horseshoe bats (Mammalia: Chiroptera) from Lesotho

Figure 6: Maximum likelihood tree of reconstructed phylogenetic relationships of the Lesotho horseshoe bats with species of the fumigatus group and other Rhinolophus groups based on the nuclear dataset. Branch support values are shown by pie charts on the nodes.

Figure 5 in On the systematic position of the horseshoe bats (Mammalia: Chiroptera) from Lesotho

Figure 5: Maximum likelihood tree of reconstructed phylogenetic relationships of the Lesotho horseshoe bats with species of the fumigatus group and other Rhinolophus groups based on the Cyt-b dataset. Branch support values are shown by pie charts on the nodes.

Figure 4 in On the systematic position of the horseshoe bats (Mammalia: Chiroptera) from Lesotho

Figure 4: Bivariate plot of skull dimensions of the examined samples of the Lesotho bats and comparative taxa: condylocanine length of skull (LCc) against length of the upper tooth-row (CM3); values in millimetres. Explanations: Lesotho I = samples from Lesotho examined by molecular genetic analysis; Lesotho II = samples from Lesotho examined only by the morphological analysis; Namibia 0 = samples of R. damarensis examined only by the morphological analysis; Namibia 1 = samples of R. damarensis of the Namibia 1 lineage; Namibia 2 = samples of R. damarensis of the Namibia 2 lineage; damarensis T = holotype specimen of Rhinolophus darlingi damarensis; S Africa II = extremely small-sized specimens from South Africa (Free State) originally identified as R. clivosus (see text for details).

Figure 2 in On the systematic position of the horseshoe bats (Mammalia: Chiroptera) from Lesotho

Figure 2: Bivariate plot of skull dimensions of the examined samples of the Lesotho bats and comparative taxa: first two roots of the principal component analysis of 15 plain skull dimensions; for explanations see Figure 1.

Figure 3 in The bat Tonatia bidens (Phyllostomidae) as an insect pest predator in the Brazilian Caatinga

Figure 3: Temporal distribution of insect remains preyed upon by Tonatia bidens in the Brazilian Caatinga. (A) Richness, number of insect remains, and monthly rainfall recorded in each sampled month. (B) Richness and number of insect remains in the dry (September and October 2016, March and August 2017) and rainy (May and November 2022) seasons, considering all data gathered. Rainfall data from https://www.apac.pe.gov. br.

Figure 7 in On the systematic position of the horseshoe bats (Mammalia: Chiroptera) from Lesotho

Figure 7: Map of localities of the examined specimens of Rhinolophus acrotis (diamonds), R. damarensis (squares) and R. cervenyi sp. n. (circles) in southern Africa (A) and in Lesotho (B); L, Lesotho; M, Mozambique; SZ, Eswatini. Open symbols – localities of origin of the specimens examined by the molecular genetic methods (except those of R. acrotis), numbers at the symbols correspond with the mitochondrial haplotype numbers as in Figure 5 and Table S1, number script denotes the lineage assignation: regular – Namibia1, bold – Namibia2, italics – South Africa & Lesotho bats. Small letters denote known localities of R. cervenyi sp. n.: Lesotho (B): a – Ha Mokoto, b – Ha Natla, c – Hermon, d – Mateanong, e – Moqotoane, f – Mount Moorosi, g – Nkokamele, h – Phallang, i – Roma, cave, j – Sehlabathebe NP, lodge, k – Semonkong, l – Ski Lodge, Oxbow; South Africa (A): m – Jagersfontein, n – Uintjiesburg.

Figure 12 in On the systematic position of the horseshoe bats (Mammalia: Chiroptera) from Lesotho

Figure 12: Occlusal views on the mesial part of the left upper tooth-row (C–M1) and the right lower toothrow (I –M) of Rhinolophus cervenyi sp. n. 3 1 (NMP 97760, holotype). Scale bar: 2 mm.

Figure 3 in Importance of riparian vegetation and wood-pastures in the maintenance of bat assemblages in a highly fragmented landscape in Veracruz, Mexico

Figure 3: Rank abundance curves of bats captured in wood-pastures (A) and riparian vegetation (B) in Jamapa, Veracruz, Mexico. Numbers indicate species, 1: Artibeus jamaicensis, 2: Sturnira parvidens, 3: A. lituratus, 4: S. hondurensis, 5: Glossophaga soricina, 6: G. commissarissi, 7: Rhogeesa tumida, 8: Desmodus rotundus, 9: Phyllostomus discolor, 10: Eptesicus furinalis, 11: Carollia sowelli, 12: A. phaeotis, 13: Uroderma bilobatum, 14: Molossus rufus, 15: C. perspicillata, 16: Chiroderma salvini, 17: A. watsoni, 18: C. villosum, 19: Pteronotus parnelli, 20: Platyrrhinus helleri, 21: Micronycteris microtis, 22: A. toltecus, 23: Centurio senex, 24: P. davyi, 25: Mormoops megallophylla, 26: Eumops bonariensis, 27: Promops centralis, 28: Myotis californicus, 29: M. keaysi.

Figure 1 in The bat Tonatia bidens (Phyllostomidae) as an insect pest predator in the Brazilian Caatinga

Figure 1: Abundance of remains of different lepidopteran taxa sampled under feeding perches of the bat Tonatia bidens, in the Brazilian Caatinga. Data collected in September and October 2016, March and August 2017, and May and November 2022. Undet. = undetermined. Lepidopteran silhouettes were used under CC0 1.0 license (www.phylopic.org).

Figure 1 in On the systematic position of the horseshoe bats (Mammalia: Chiroptera) from Lesotho

Figure 1: Bivariate plot of skull dimensions of the examined samples of the Lesotho bats and comparative taxa: condylocanine length of skull (LCc) against length of the upper tooth-row (CM3); values in millimetres. Explanations: Abyssinia = samples of R. acrotis acrotis from Ethiopia, Eritrea and the Sudan; E Africa = samples of R. acrotis augur from East Africa (Uganda, Kenya, Rwanda, Tanzania, Malawi); S Africa = samples of R. acrotis augur from southern Africa (Mozambique, South Africa); types = holotype specimens of Rhinolophus augur (G), Rhinolophus augur zambesiensis (B), Rhinolophus augur zuluensis (U), and Rhinolophus darlingi damarensis (D); S Africa II = extremely small-sized specimens from South Africa originally identified as R. clivosus (see text for details); polygon = range extremes of the values for R. damarensis from Namibia.

Figure 2 in Filling the gap of distribution of the pale-winged dog-like bat Peropteryx pallidoptera (Chiroptera, Emballonuridae) in Brazil and Peru

Figure 2: Specimens of Peropteryx pallidoptera sampled in Brazilian Amazon. (A–B) Adult female (IDSM 03258) captured at Juami-Japurá Ecological Station, Amazonas (photos by Tamily C.M. Santos and Gerson P. Lopes); (C) adult male (MZUSP 35757) captured at Machadinho D'Oeste, Rondônia (photo by Vinícius C. Cláudio); (D) adult female at Sacará-Taquera National Forest, Pará (photo by Andrezza S.V. Hirota).