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240 results for “Hipposideridae”

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zenodo32/100

Distribution. C, E & S in Hipposideridae

Distribution. C, E & S China (including Hainan I) and N Vietnam; a record from N Myanmar has not been confirmed.

opennotspecifiedOct 2019View details →
zenodo32/100

Supplementary material 3 from: Patterson BD, Webala PW, Lavery TH, Agwanda BR, Goodman SM, Kerbis Peterhans JC, Demos TC (2020) Evolutionary relationships and population genetics of the Afrotropical leaf-nosed bats (Chiroptera, Hipposideridae). ZooKeys 929: 117-161. https://doi.org/10.3897/zookeys.929.50240

Figure S3. Phylogeny of Hipposideridae based on Bayesian inference analysis of cyt-b based on 452 individuals

opencc-zeroApr 2020View details →
zenodo32/100

Supplementary material 2 from: Patterson BD, Webala PW, Lavery TH, Agwanda BR, Goodman SM, Kerbis Peterhans JC, Demos TC (2020) Evolutionary relationships and population genetics of the Afrotropical leaf-nosed bats (Chiroptera, Hipposideridae). ZooKeys 929: 117-161. https://doi.org/10.3897/zookeys.929.50240

Figure S2. Phylogeny of Hipposideridae based on maximum likelihood analysis of cyt-b based on 452 individuals

opencc-zeroApr 2020View details →
zenodo32/100

FIG. 5 in Description of a new species of the genus Aselliscus (Chiroptera, Hipposideridae) from Vietnam

FIG. 5. Portraits and skull photographs of A. stoliczkanus s.l. A — A. stoliczkanus (IEBR-T5024, ♂) and B — A. dongbacana sp.n. (holotype IEBR-VN11-0143, ♂)

opennotspecifiedNov 2015View details →
zenodo32/100

FIG. 1 in Description of a new species of the genus Aselliscus (Chiroptera, Hipposideridae) from Vietnam

FIG. 1. Distribution area (dot line) of Aselliscus stoliczkanus s.l. (Li et al., 2007; Bates et al., 2008) and taxonomic sampling used for this study. Map of karst (shaded) in the mainland of Southeast Asia (modified from Ford and Williams, 2007). Type locality: A. stoliczkanus (circle, in red); A. wheeleri (full square, in red). Symbols represent the geographical origins of bats of clade A (full circles) and clade B (empty diamonds) of A. stoliczkanus identified by genetic and morphological analyses (Figs. 2 and 4). Clade A: Subclade A1 (1 — Sai Yok; 2 — Dakrong; 3 — Bac Huong Hoa; 4 — Phong Nha - Ke Bang; 5, 6, 7 — Hin Nam No region; 8 — Phou Khao Khouay; 9 — Luoang Phrabang; 10 — Xuan Lien; 11 — Ngoc Lac; 12 — Cuc Phuong; 13 — Xuan Son; 14 — Nam Et NBCA; 19 — Ta Phin, Sa Pa); Subclade A2 (21 — Yunnan (Li et al., 2007)); Subclade A3 (20 — Yunnan (Sun et al., 2009); 22 — Guizhou; and 24 — Shichuan); Subclade A4 (23 — Guizhou, Libo) and Subclade A5 (15 — Louang Namtha; 16, 17, 18 — Myanmar); Clade B: 25 — Khau Ca; 26 — Phia Oac-Phia Den; 27 — Ba Be; 28 — Na Hang; and 29 — Huu Lien

opennotspecifiedNov 2015View details →
zenodo32/100

FIG. 4 in Description of a new species of the genus Aselliscus (Chiroptera, Hipposideridae) from Vietnam

FIG. 4. Principal components analyses (PCA) of studied Aselliscus spp. A — PCA based on eight external characters; B–E — PCAs based on datasets of a reduction from 10 to three craniodental characters

opennotspecifiedNov 2015View details →
zenodo32/100

IV in Description of a new species of the genus Aselliscus (Chiroptera, Hipposideridae) from Vietnam

IV Chronogram reconstructed from the Cytb dataset for Aselliscus spp. and associated outgroups. Mean divergence values (expressed as million year ago, Mya) are given at each node and horizontal bars represent the 95% highest posterior density ranges. Clade names of A. stoliczkanus s.l. correspond to those given in Fig. 2

opennotspecifiedNov 2015View details →
zenodo32/100

III Average nucleotide distances (%) based on the Kimura 2-parameter (K2P) model between Aselliscus spp., and associated outgroups based on complete mitochondrial Cytb (1,140 bp, below the diagonal) and COI (657 bp, above the diagonal) gene sequences in Description of a new species of the genus Aselliscus (Chiroptera, Hipposideridae) from Vietnam

III Average nucleotide distances (%) based on the Kimura 2-parameter (K2P) model between Aselliscus spp., and associated outgroups based on complete mitochondrial Cytb (1,140 bp, below the diagonal) and COI (657 bp, above the diagonal) gene sequences

opennotspecifiedNov 2015View details →
zenodo32/100

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

opennotspecifiedMar 2006View details →
zenodo32/100

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

opennotspecifiedMar 2006View details →
zenodo32/100

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

opennotspecifiedMar 2006View details →
zenodo32/100

FIG. 3 in A new species of Hipposideros (Chiroptera: Hipposideridae) from Sulawesi

FIG. 3. Dorsal (above) and ventral (below) views of the skull and dorsal view of the right half mandible of two species of Hipposideros. A — H. boeadii (holotype), M28253, Rawa Aopa Watumohai National Park, South-

opennotspecifiedMar 2007View details →
zenodo32/100

FIG. 2 in A new species of Hipposideros (Chiroptera: Hipposideridae) from Sulawesi

FIG. 2. Noseleaves of four species of Hipposideros (with hairs omitted). A — H. boeadii (holotype), M28253, Rawa Aopa Watumohai National Park, South-East Sulawesi; B — H. papua, M16951, Biak Island, Papua Province; C — H. galeritus, M28250, Kakenauwe Nature Reserve, Buton Island, South- East Sulawesi; D — H. cervinus, M28249, Lambasango Wildlife Reserve, Buton Island, South- East Sulawesi. Scale = 5 mm

opennotspecifiedMar 2007View details →
zenodo32/100

FIG. 5 in A new species in the Hipposideros bicolor group (Chiroptera: Hipposideridae) from Peninsular Malaysia

FIG. 5. Distribution of echolocation call frequencies and lengths of forearm for all H. bicolor captured in peninsular Malaysia for which echolocation call data were available. H. bicolor (=H. bicolor-131; open squares), H. kunzi sp. nov. (=H. bicolor- 142; crosses), and unidentified individuals with intermediate call frequency (solid circles) were included

opennotspecifiedDec 2018View details →
zenodo32/100

FIG. 4 in A new species in the Hipposideros bicolor group (Chiroptera: Hipposideridae) from Peninsular Malaysia

FIG. 4. Results of the statistical parsimony analysis for H. kunzi sp. nov. (=H. bicolor-142) recovered two groups, separated by the dashed line (15 steps). Solid lines represent one base pair change. Haplotypes Z and Y are from southern Thailand, haplotypes S, T, U, V, W, and X represent the Perlis group, and all other haplotypes are part of the Malay group. Haplotype A was determined to be the most basal in this analysis

opennotspecifiedDec 2018View details →
zenodo32/100

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

opennotspecifiedMay 2009View details →
zenodo32/100

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 (-)

opennotspecifiedMay 2009View details →
zenodo32/100

List of tissue specimens of Hipposideros spp. used for cytochrome b sequencing and phylogenetic inference, with geographical data. Voucher refers to the location and/or accession number of the voucher, and tissue collection refers to the collection where the tissue is kept, and accession or collector numbers. Acronyms are as follows: Estación Biológica de DoZana, Sevilla, Spain (EBD), South Australia Museum, Adelaide, Australia (SAM), Senckenberg Museum, Frankfurt am Main, Germany (SMF), Instituto de Ecología, Xalapa, México (IEX), Louisiana State University, Baton Rouge, Louisiana, USA (LSU), Charles M. Francis, Canadian Wildlife Service, Ottawa, Ontario, Canada (CMF), Lao Department of Forestry, Vientiane, Lao PDR, no catalogued (LAO). Next column indicates GenBank accession numbers. More information about the specimens is available in the GenBank records in A new species of bat of the Hipposideros bicolor group (Chiroptera: Hipposideridae) from Central Laos, with evidence of convergent evolution with Sundaic taxa

List of tissue specimens of Hipposideros spp. used for cytochrome b sequencing and phylogenetic inference, with geographical data. Voucher refers to the location and/or accession number of the voucher, and tissue collection refers to the collection where the tissue is kept, and accession or collector numbers. Acronyms are as follows: Estación Biológica de DoZana, Sevilla, Spain (EBD), South Australia Museum, Adelaide, Australia (SAM), Senckenberg Museum, Frankfurt am Main, Germany (SMF), Instituto de Ecología, Xalapa, México (IEX), Louisiana State University, Baton Rouge, Louisiana, USA (LSU), Charles M. Francis, Canadian Wildlife Service, Ottawa, Ontario, Canada (CMF), Lao Department of Forestry, Vientiane, Lao PDR, no catalogued (LAO). Next column indicates GenBank accession numbers. More information about the specimens is available in the GenBank records

opennotspecifiedMar 2006View details →
zenodo32/100

FIG. 5 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. 5. Schematic drawing of rostral chambers in dorsal view, mouth above. Dotted areas correspond to dense bone and bone walls, while white areas indicate cavities. A — H. khaokhouayensis ROM 116793; B — H. rotalis IEX-M0095, ♀; C — H. orbiculus SMF 57092; D — H. ridleyi SMF 69291. a) Anterior rostral chamber, b) Postero-lateral rostral chamber, c) and c') postero-median rostral chamber. Notice that in A and B the posterior chambers are not separated by the intermediate wall, and that in D, the posterior median chamber is split in two, c and c'

opennotspecifiedMar 2006View details →
zenodo32/100

FIG. 8 in Taxonomic revision of the genus Asellia (Chiroptera: Hipposideridae) with a description of a new species from southern Arabia

FIG. 8. Median-joining network of Middle Eastern and African Asellia haplotypes. Solid lines indicate one substitution. Dashed lines are not proportional to the evolutionary change, but the numbers of substitutions are indicated numerically. The size of the nodes corresponds to the frequency of the particular haplotype. Solitary haplotypes are left blank, more frequent haplotypes are labelled according to Appendix II

opennotspecifiedMar 2011View details →

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