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FIGURE 7 in A new species of lobe-lipped bat (Chalinolobus: Vespertilionidae) from southern Papua New Guinea
FIGURE 7. Plot of specimen scores for the first three axes of a PCA based on a correlation matrix of FA and six skull and dental measurements of 29 Chalinolobus skulls: a) PC 1 vs. PC 2, and b), PC 1 vs. PC 3. Symbols are: C. orarius sp. nov. (rectangles), Australian C. nigrogriseus (circles), Chalinolobus from PNG of indeterminate species previous referred to C. nigrogriseus (inverted triangles), and C. gouldii from northern Australia (triangles) including the type series of C. gouldii venatoris (diamonds). Solid symbols are male, open symbols female. 1, C. sp. indet. (AMNH 193793 female) from Port Moresby, PNG.
FIGURE 6 in A new species of lobe-lipped bat (Chalinolobus: Vespertilionidae) from southern Papua New Guinea
FIGURE 6. Plot of specimen scores for the first three axes of a PCA based on a correlation matrix of four skull and dental measurements of 47 Chalinolobus skulls: a) PC 1 vs. PC 2, and b), PC 1 vs. PC 3. Symbols are: C. orarius sp. nov. (rectangles), Australian C. nigrogriseus (circles), Chalinolobus from PNG of indeterminate species previous referred to C. nigrogriseus (inverted triangles), and C. gouldii from southern Australia (hexagons) and northern Australia (triangles), including the type series of C. gouldii venatoris (diamonds). Solid symbols are male, open symbols female. 1, holotype of C. nigrogriseus, 2, holotype of C. orarius sp. nov. and 3, holotype of C. gouldii venatoris.
FIGURE 5 in A new species of lobe-lipped bat (Chalinolobus: Vespertilionidae) from southern Papua New Guinea
FIGURE 5. Trends of a relatively broader rear palate of C. sp. compared to: a), northern C. gouldii as seen in a plot of maximum breadth from left M3 to right M3 (M3–M3) vs. Outer breadth across upper canines (C1–C1); and b), C. nigrogriseus, from a plot of maxillary tooth row length (CM3) vs. M3–M3.
FIGURE 4 in A new species of lobe-lipped bat (Chalinolobus: Vespertilionidae) from southern Papua New Guinea
FIGURE 4. Trends in differing skull proportions of C. sp.: a), least intertemporal breadth (INT) vs. condylobasal length (CON), showing relatively broader INT than northern C. gouldii; b), CON vs. mastoid breadth (MASB) showing relatively broader MASB than northern C. gouldii and C. nigrogriseus; c), CON vs. zygomatic breadth (ZYG) showing relatively broader ZYG than northern C. gouldii and C. nigrogriseus.
FIGURE 3 in A new species of lobe-lipped bat (Chalinolobus: Vespertilionidae) from southern Papua New Guinea
FIGURE 3. Intermediate body size of C. sp. (rectangles) between C. nigrogriseus and C. gouldii exemplified by: a), Forearm length (FA) vs. Outside breadth across upper canines (C1–C1) for adult males (solid symbols) and females (open symbols). Type specimens are: 1, C. orarius sp. nov. holotype; 2, C. nigrogriseus holotype, sex unknown; 3, C. gouldii venatoris holotype, and 4, C. gouldii lectotype, sex unknown; and b), field forearm length (FA) vs. field body weight (WT) for adult females. Symbols are: Australian C. nigrogriseus (circles), C. sp. indet. PNG (inverted triangles); C. gouldii from southern Australia (hexagons), and northern Australia (triangles) including the type series of C. gouldii venatoris (diamonds). Additional symbols for Fig. 3b are: C. nigrogriseus from WA, NT and Gulf of Carpentaria (dotted circles); C. gouldii northern from Cape Cleveland, NT (crosses, n = 5, Glenn Hoye pers. comm.), and an adult female from Port Essington, NT from Calaby & Keith (1974), solid inverted triangle.
FIGURE 9 in A new species of lobe-lipped bat (Chalinolobus: Vespertilionidae) from southern Papua New Guinea
FIGURE 9. Holotype of C. orarius sp. nov., AM M.15114 adult male from Port Moresby, PNG. (Photo: Ron Lovatt, AM Digivols).
FIGURE 1 in A new species of lobe-lipped bat (Chalinolobus: Vespertilionidae) from southern Papua New Guinea
FIGURE 1. Locality records of Chalinolobus from Papua New Guinea, showing Province boundaries. Six localities from Port Moresby environs (inset map) are: 1, Waigani Sewerage works, 2, National Museum & Art Gallery roof, 3, Gordon, 4, Saraga, 5, Champion House, and 6, Paga Hill Court House.
Old world fruit bat body mass: bat-body-masses.txt.gz
Open the record for dataset details and reuse information.
Fig. 1. A in Postnatal Growth and Vocalization Development in the Long-fingered Bat, Myotis capaccinii (Chiroptera, Vespertilionidae)
Fig. 1. A comparison between echolocation calls of an adult and newborn long-fingered bat, Myotis capaccinii. (a) Sonogram, showing calls composed of a frequency modulation (FM) component with a variable range of frequencies. (b) Power spectrogram, showing the dominant frequency of the call.
Fig. 4 in Postnatal Growth and Vocalization Development in the Long-fingered Bat, Myotis capaccinii (Chiroptera, Vespertilionidae)
Fig. 4. Positive associations between changes in the peak frequency and handwing area, armwing area and aspect ratio. Negative associations are illustrated between changes in the peak frequency and wing loading.
Fig. 3 in Postnatal Growth and Vocalization Development in the Long-fingered Bat, Myotis capaccinii (Chiroptera, Vespertilionidae)
Fig. 3. Positive associations between changes of the peak frequency of calls emitted by Myotis capaccinii infants with (a) forearm length, (b) body mass, (c) wing area and (d) wingspan from day 1-28.
Fig. 2 in Postnatal Growth and Vocalization Development in the Long-fingered Bat, Myotis capaccinii (Chiroptera, Vespertilionidae)
Fig. 2. Changes in the calls emitted by Myotis capaccinii infants during postnatal growth from day 1-16.
Fig. 5 in Postnatal Growth and Vocalization Development in the Long-fingered Bat, Myotis capaccinii (Chiroptera, Vespertilionidae)
Fig. 5. Recording calls by a mother-infant pair when the infant bat is separating from its mother and modes before and after separation from its mother. One to two harmonic calls with high-frequency in the before and after separation step belong to the mother and multiharmonic calls with low-frequency belong to the pup.
Figure 2 in Diurnal activity of a trawling insectivorous bat species, Myotis horsfieldii, in Gunung Mulu National Park, Malaysian Borneo
Figure 2. Feeding buzz of Myotis horsfieldii, observed at Site 13 in the Gunung Mulu National Park, recorded between 11.00 and 11.30am on 17 July 2020.
Figure 3 in Diurnal activity of a trawling insectivorous bat species, Myotis horsfieldii, in Gunung Mulu National Park, Malaysian Borneo
Figure 3. The microhabitats where the diurnal bats were observed in Gunung Mulu National Park: (A) – river with high canopy cover in the forest interior (Site 1), (B) – pool with high canopy shade (Site 6), (C) – river with low canopy cover at the forest edge (Site 9), (D) – river with low canopy shade in fragmented forest (Site 12).
Figure 1 in Diurnal activity of a trawling insectivorous bat species, Myotis horsfieldii, in Gunung Mulu National Park, Malaysian Borneo
Figure 1. Records of daylight activity of Horsfield's bat (Myotis horsfieldii) in Gunung Mulu National Park, in Malaysian Borneo. The circles denote visual records, the triangles denote acoustic records, and the squares denote records by both visual and acoustic inspection.
Figure 2 in A multidisciplinary approach unveils the distribution of the Alpine long-eared bat Plecotus macrobullaris (Vespertilionidae) in Italy
Figure 2: Phylogenetic analyses of long-eared bats. (Left) origin of molecular samples analysed from Italy; (right) bootstrapped consensus ML phylogenetic tree (10,000 iterations) obtained from the analysis of COI gene fragment of Plecotus bats. Coloured sequences represent new genetic sequences and refer to different species. The statistical support of major clades is shown at their nodes (ML bootstrap support).
Figure 2 in First record of Great Himalayan leaf-nosed bat, Hipposideros armiger (Hipposideridae) from Bangladesh
Figure 2: Image showing the supplementary nose-leaf and fleshy outgrowth of Hipposideros armiger captured from the cave in the Sadar Upazila subdistrict of Bandarban district, Bangladesh.
Figure 1 in First record of Great Himalayan leaf-nosed bat, Hipposideros armiger (Hipposideridae) from Bangladesh
Figure 1: Location of the cave in the Sadar Upazila subdistrict of Bandarban district, Bangladesh and global range of Hipposideros armiger according to Bates et al. (2020).
Figure 1 in Observations of a greater sac-winged bat pup (Saccopteryx bilineata) with a chromatic disorder
Figure 1: Saccopteryx bilineata pup in its day-roost with normal pigmentation (A). The wavy white lines are only faint and not yet pronounced like in adult bats. Photo credit: S. Ripperger. Mother-pup pair in a day roost (B). The mother is clearly distinguishable from the pup by her brown fur and the pronounced white lines on the back. Since this pup is older the faint white lines are also starting to appear on its back. Photo credit: M. Stifter.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
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
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.