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APPENDIX Locality details for Murina mapped in Figs. 1 and 2a. Details for the remaining species in Fig. 2 are given in the text in A review of tube-nosed bats (Murina) from Laos with a description of two new species
APPENDIX Locality details for Murina mapped in Figs. 1 and 2a. Details for the remaining species in Fig. 2 are given in the text
FIG. 6 in A review of tube-nosed bats (Murina) from Laos with a description of two new species
FIG. 6. Photographs of four species of Murina in life from Laos: (a) M. walstoni ROM 110450; (b) M. fionae sp. nov. ROM 106382 or 106383; (c): M. cyclotis ROM 110647; (d) M. feae ROM 110476
FIG. 2 in A review of tube-nosed bats (Murina) from Laos with a description of two new species
FIG. 2. Distribution of known specimen records of Murina from Laos and surrounding countries for (a) M. harrisoni, (b) M. walstoni, (c) M. fionae sp. nov., and (d) M. annamitica sp. nov. Solid circles (●) represent locations for specimens examined by the authors from Laos and surrounding countries (see Appendix and text for specimen details). Solid stars represent type localities for each species. Hollow circles represent records from the published literature. On map (a), the open star marks the type locality for M. tiensa, here considered a synonym of M. harrisoni, while the open circle marks the location of additional material referred to M. tiensa by Csorba et al. (2007)
FIG. 5 in A new species of South-East Asian Myotis (Chiroptera: Vespertilionidae), with comments on Vietnamese 'whiskered bats'
FIG. 5. Camera lucida tracings of the skull of M. annatessae sp. nov. (paratype ZMMU S-165043). Scale bar = 5 mm
FIG. 4 in A new species of South-East Asian Myotis (Chiroptera: Vespertilionidae), with comments on Vietnamese 'whiskered bats'
FIG. 4. Neighbour-joining tree of COI sequences of 25 species of Eurasian Myotis included in comparative molecular analysis (see Appendix for list of sequences used). Only bootstrap supports over 70% are shown
FIG. 2. Bivariate scatterplot for the 1 in A new species of South-East Asian Myotis (Chiroptera: Vespertilionidae), with comments on Vietnamese 'whiskered bats'
FIG. 2. Bivariate scatterplot for the 1st and 2nd Principal Components, calculated for 20 cranial and dental measurements of 100 specimens of small Asian mouse-eared bats. For factor loadings and eigenvalues, see Table 1
FIG. 3 in A new species of South-East Asian Myotis (Chiroptera: Vespertilionidae), with comments on Vietnamese 'whiskered bats'
FIG. 3. Camera lucida traces of penial bones (bacula) in five smaller species of the Asiatic Myotis: a, b — M. annatessae sp. nov., Vietnam, ZMMU S-164989 (dorsal, ventral, right lateral views), ZMMU S-165043 (dorsal, ventro-lateral, right lateral views); c — M. ater, Vietnam, ZMMU S-172604 (dorsal, right lateral views); d — M. siligorensis, Vietnam, ZMMU S-167188 (ventral, left lateral views); e, f, g — M. muricola, Vietnam, ZMMU S-172616 (dorsal, right lateral views), ZMMU S-173413 (dorsal, ventrolateral, left lateral views), ZMMU S-172626 (dorsal, right lateral views); h — M. muricola, Nepal, ZMMU S-164491 (dorsal, right ventro-lateral views)
FIG. 4 in A review of tube-nosed bats (Murina) from Laos with a description of two new species
FIG. 4. Upper left toothrows of specimens of eight species of Murina from Laos: (a) M. harrisoni, EBD 24974; (b) M. fionae sp. nov. ROM 106383; (c) M. huttoni ROM 106419; (d) M. cyclotis, ROM 106431; (e) M. annamitica sp. nov., ROM 106467; (f) M. eleryi, ROM 106411; (g) M. walstoni ROM 110450; (h) M. feae, ROM 106477. Scale bar = 5 mm
inBolikhamsai includedtaxa, ofKading comparisonsNam — K pairwise; Malaysia allEast for,)Sabah studies— otherS; withMalaysia comparisonPeninsularfor— ratesM: equalsamplewiththe,of1983origin, NeiofandregionTamuraindicate(distancesnamegeneticspeciesPercentageafterLetters.. 2studyABLE the T in A new species of bat of the Hipposideros bicolor group (Chiroptera: Hipposideridae) from Central Laos, with evidence of convergent evolution with Sundaic taxa
inBolikhamsai includedtaxa, ofKading comparisonsNam — K pairwise; Malaysia allEast for,)Sabah studies— otherS; withMalaysia comparisonPeninsularfor— ratesM: equalsamplewiththe,of1983origin, NeiofandregionTamuraindicate(distancesnamegeneticspeciesPercentageafterLetters.. 2studyABLE the T
FIG. 1 in A new species of bat of the Hipposideros bicolor group (Chiroptera: Hipposideridae) from Central Laos, with evidence of convergent evolution with Sundaic taxa
FIG. 1. Map of Southeast Asia with some of the Sunda islands showing the distribution records of H. ridleyi (diamonds), H. orbiculus (squares), H. rotalis (black and hollow circles), and the new species described here (black circles). The distribution of the first three species was reviewed by Francis et al. (1999). Notice that the black circles correspond to new localities recorded in the present study, where both H. rotalis and the new species were captured
Fig. 4 in A new species of bat of the Hipposideros bicolor group (Chiroptera: Hipposideridae) from Central Laos, with evidence of convergent evolution with Sundaic taxa
Fig. 4. View of skull of the holotype of H. khaokhouayensis (ROM 116790, Field No. CMF980203-29). A — dorsal view, B — ventral view, C — dorsal view of mandible, D — lateral view of skull with mandible. White scales are 10 mm long with tick marks spaced 1 mm
FIG. 4 in A new species of tube-nosed bat Murina (Vespertilionidae, Chiroptera) from Vietnam
FIG. 4. Comparison of the upper tooth rows and palate shape among some Murina species: A — M. harpioloides sp. nov., holotype; B — M. aurata, ROM MAM-111386; C — M. ussuriensis, ZMMU S-173249; D — M. tubinaris, ROM MAM-111302; E —
FIG. 1 in A recent inventory of the bats of Mozambique with documentation of seven new species for the country
FIG. 1. Map of Mozambique showing the sites at which bats were captured during this study (2005–2009). The sampling sites are overlaid on a digital elevation model (altitude in metres). The boundaries of the three biogeographic zones (following Parker, 1999) are represented by the two black lines. The southern line follows the Save River, whereas the northern line follows the Zambezi
FIG. 8 in Late Middle Eocene bats from the Creechbarrow Limestone Formation, Dorset, southern England with description of a new species of Archaeonycteris (Chiroptera: Archaeonycteridae)
FIG. 8. Trigonids of lower molars, Creechbarrow bats. Rhinolophidae gen. et sp. indet. M35711. Trigonid left lower molar in A — occlusal, B — buccal and C — lingual views. HZM 2.38159. Trigonid right lower molar in D — occlusal, E — buccal and F — lingual views. Microchiroptera gen. et sp. indet. HZM 22.34774. Trigonid right lower molar in G — occlusal, H — buccal
F. 4. Pseudorhinolophus schlosseri, Creechbarrow. HZM 1.31792. Left M2 in Late Middle Eocene bats from the Creechbarrow Limestone Formation, Dorset, southern England with description of a new species of Archaeonycteris (Chiroptera: Archaeonycteridae)
F. 4. Pseudorhinolophus schlosseri, Creechbarrow. HZM 1.31792. Left M2: A — occlusal and B — oblique distal views. HZM IG 3.38170. Left M1/2 in C — distal, D — lingual, E — buccal and F — occlusal views. Rhinolophidae gen. et sp. indet. HZM 1.31222.
FIG. 2 in Recent surveys of bats (Mammalia: Chiroptera) from China. I. Rhinolophidae and Hipposideridae
FIG. 2. Representative echolocation calls of bats in the family Rhinolophidae captured from China during our surveys (except Rhinolophus stheno for which sound files were unavailable). See text for data on intraspecific variation. Recordings are from time expanded sequences of handheld bats with FFT size 1024 Hz, Hanning window. The species are arranged according to body size
FIG. 3 in A recent inventory of the bats of Mozambique with documentation of seven new species for the country
FIG. 3. Ventral (A) and lateral (B) views of the baculum of R. cf. deckenii (DM 8560), from Chinizuia, central Mozambique. One small square on the graph paper represents 1 mm
FIG. 1 in Late Middle Eocene bats from the Creechbarrow Limestone Formation, Dorset, southern England with description of a new species of Archaeonycteris (Chiroptera: Archaeonycteridae)
FIG. 1. Archaeonycteris relicta sp. nov., Creechbarrow, mandibular cheekteeth. HZM 4.37495. Right P2 in A — occlusal, B — buccal and C — lingual views. Scale = 0.5 mm. HZM 5.38291. Left M3 (holotype) D — distal, E — lingual, F — buccal and G — occlusal
FIG. 3 in Recent surveys of bats (Mammalia: Chiroptera) from China. I. Rhinolophidae and Hipposideridae
FIG. 3. Relationship between frequency of echolocation calls from handheld bats (resting frequency) and forearm length for Rhinolophus sinicus (D) and R. affinis (-)
FIG. 5 in Bat diversity in the Simandou Mountain Range of Guinea, with the description of a new white-winged vespertilionid
FIG. 5. Dorsal and ventral view of a live-captured N. tenuipinnis from Liberia. Note the dark dorsal fur (Photographs by A. Monadjem)
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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.