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Subspecies and Distribution. R d. denti Thomas, 1904 - SW Angola, N Namibia, NW & SW Botswana, and N South Africa (Northern Cape Province). There is an unconfirmed record from SW Republic of the Congo. R d. knorri Eisentraut, 1960 - scattered records across W Africa in SE Senegal, Guinea-Bissau, W Guinea, N Sierra Leone, N Ivory Coast (but possibly representing Lander's Horseshoe Bat, R landeri), NE Ghana, S Burkina Faso, and Nigeria. There is apparently a specimen from S South Sudan that might represent this subspecies, although its identity needs to be validated. in Rhinolophidae
Subspecies and Distribution. R d. denti Thomas, 1904 - SW Angola, N Namibia, NW & SW Botswana, and N South Africa (Northern Cape Province). There is an unconfirmed record from SW Republic of the Congo. R d. knorri Eisentraut, 1960 - scattered records across W Africa in SE Senegal, Guinea-Bissau, W Guinea, N Sierra Leone, N Ivory Coast (but possibly representing Lander's Horseshoe Bat, R landeri), NE Ghana, S Burkina Faso, and Nigeria. There is apparently a specimen from S South Sudan that might represent this subspecies, although its identity needs to be validated.
Fig. Sa/b: (a) Strict consensus of 2 most parsimonious trees generated by exact analysis of sequence data. Numbers on branches represent bootstrap node confidence values from 100 replications. (b) Jac support tree. Numbers on branches represent confidence frequencies in nodes as quantified by parsimony jacknifing with Jac (Farris 1995). in Morphological and mitochondrial-DNA variation in Rhinolophus rouxii (Chiroptera)
Fig. Sa/b: (a) Strict consensus of 2 most parsimonious trees generated by exact analysis of sequence data. Numbers on branches represent bootstrap node confidence values from 100 replications. (b) Jac support tree. Numbers on branches represent confidence frequencies in nodes as quantified by parsimony jacknifing with Jac (Farris 1995).
FIG. 1. Bayesian consensus topology with support values for major nodes. Values above indicate posterior probabilities and values below represent 1,000 in Diversity of Hipposideridae in the Mount Nimba massif, West Africa, and the taxonomic status of Hipposideros lamottei
FIG. 1. Bayesian consensus topology with support values for major nodes. Values above indicate posterior probabilities and values below represent 1,000 bootstraps. An 'X' indicates that the node was not recovered in the respective analysis
APPENDIX Individuals included in the genetic and/or skull morphology analyses are presented with source and locality information (reference to sites in Fig. 1 are given in parentheses when available). Voucher numbers are provided for individuals that were collected: AMNH — American Museum of Natural History, New York, NY, USA, BMNH — Natural History Museum, London, UK, FMNH — Field Museum, Chicago, IL, USA, HZM — Harrison Zoological Museum, Kent, UK, MCZ — Museum of Comparative Zoology, Harvard, MA, USA, MZB — Muzeum Zoologicum Bogoriense, Bogor, Indonesia, RMNH — National Museum of Natural History Naturalis, Leiden, Netherlands, SEN — Senckenberg Museum, Frankfurt, Germany, TK — tissue collection and TTU — specimen numbers; Texas Tech. University, Lubbock, TX, USA, and USNM — Smithsonian Institute, Washington D.C., USA. All specimens from peninsular Malaysia with THK or MBCRU field numbers were collected by A. Zubaid, and the specimens or duplicate wing punches were deposited at UKM (Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia). The original taxonomy of type specimens (type) are listed. Haplotypes (Hap) are given for individuals of H. bicolor (=H. bicolor-131) and H. kunzi (=H. bicolor-142). GenBank accession numbers are given for one representative of each unique haplotype in A new species in the Hipposideros bicolor group (Chiroptera: Hipposideridae) from Peninsular Malaysia
APPENDIX Individuals included in the genetic and/or skull morphology analyses are presented with source and locality information (reference to sites in Fig. 1 are given in parentheses when available). Voucher numbers are provided for individuals that were collected: AMNH — American Museum of Natural History, New York, NY, USA, BMNH — Natural History Museum, London, UK, FMNH — Field Museum, Chicago, IL, USA, HZM — Harrison Zoological Museum, Kent, UK, MCZ — Museum of Comparative Zoology, Harvard, MA, USA, MZB — Muzeum Zoologicum Bogoriense, Bogor, Indonesia, RMNH — National Museum of Natural History Naturalis, Leiden, Netherlands, SEN — Senckenberg Museum, Frankfurt, Germany, TK — tissue collection and TTU — specimen numbers; Texas Tech. University, Lubbock, TX, USA, and USNM — Smithsonian Institute, Washington D.C., USA. All specimens from peninsular Malaysia with THK or MBCRU field numbers were collected by A. Zubaid, and the specimens or duplicate wing punches were deposited at UKM (Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia). The original taxonomy of type specimens (type) are listed. Haplotypes (Hap) are given for individuals of H. bicolor (=H. bicolor-131) and H. kunzi (=H. bicolor-142). GenBank accession numbers are given for one representative of each unique haplotype
9-10-1014: The gas-phase oxidation of mixed organic films at the air-water interface – testing for cloud climate effects in more representative proxies of real clouds
<p>Binned Neutron Data for the titled experiment 9-10-014</p>
Fragment of a doorframe representing Vishnu
Fragment of a doorframe, Candella style, central India, 11th century, pink sandstone. Musée du Cinquantenaire (Brussels, Belgium). Made with ReMake and ReCap Pro from AutoDesk. This relief shows different aspects of Vishnu. Vishnu is the second god in the Hindu triumvirate (orTrimurti). The triumvirate consists of three gods who are responsible for the creation, upkeep and destruction of the world. The other two gods are Brahma and Shiva. Brahma is the creator of the universe and Shiva is the destroyer. For more updates, please consider to follow me on Twitter at @GeoffreyMarchal. Source: Objaverse 1.0 / Sketchfab
FIGURE 9 in Taraxacum mirabile, an enigmatic sexual halophilous endemic dandelion, represents a new section
FIGURE 9. Fine sculpture of achene surface of selected Taraxacum taxa other than T. mirabile, for comparison. A, Taraxacum (Atrata) chionomelas (PRA, cult. JŠ 3835). B, Taraxacum (Cucullata) cucullatum (PRA, cult. JŠ 6575). C, Taraxacum (Borysthenica) bachczisaraicum (PRA, cult. 318). D, Taraxacum (Piesis) besarabicum (PRA, cult. 308). Scale bars: A, 50 μm. B, 20 μm. C, 100 μm. D, 50 μm.
FIGURE 7. Taraxacum mirabile. A, a in Taraxacum mirabile, an enigmatic sexual halophilous endemic dandelion, represents a new section
FIGURE 7. Taraxacum mirabile. A, a detail of achene surface; Tuz Gölü (PRA, no. det. 33693). Scale bar = 0.1 mm. B, achenes; Tuz Gölü (PRA, no. det. 33693). Scale bar = 1 mm.
Figure 6. Amphibioplana onnisi. A, RMNH.VER. 19957.a in Amphibioplanidae: a new branch and family on the phylogenetic tree of the triclad flatworms (Platyhelminthes: Tricladida), represented by a species from Sardinian caves with a remarkable lifestyle
Figure 6. Amphibioplana onnisi. A, RMNH.VER. 19957.a, photomicrograph of sagittal section of the anterior end, showing dorsal (de) and ventral epidermis (ve) being uniformly clothed with cilia (c); B, RMNH.VER. 19960.g, photomicrograph of horizontal section of the posterior end, showing adhesive glands (ag) discharging their secretion through the epidermis.
Figure 7. Amphibioplana onnisi. A, holotype RMNH.VER. 19956.a in Amphibioplanidae: a new branch and family on the phylogenetic tree of the triclad flatworms (Platyhelminthes: Tricladida), represented by a species from Sardinian caves with a remarkable lifestyle
Figure 7. Amphibioplana onnisi. A, holotype RMNH.VER. 19956.a, photomicrograph of a horizontal section of the head, with the brain (b) and the post-cephalic region, also showing the anterior intestinal branch (aib), left ovary (lo) with its tuba (tu) and the first tract of the left oviduct (lod), the most anterior vitellaria (vi) and testes (t); B, RMNH.VER. 19958.f, photomicrograph of a horizontal section of the post-pharyngeal region with the copulatory apparatus, showing the most caudal vitellaria (vi) and the two caudal gut trunks fusing to form a single branch (pib).
Figure 11. Amphibioplana onnisi. A, holotype RMNH.VER. 19956.a in Amphibioplanidae: a new branch and family on the phylogenetic tree of the triclad flatworms (Platyhelminthes: Tricladida), represented by a species from Sardinian caves with a remarkable lifestyle
Figure 11. Amphibioplana onnisi. A, holotype RMNH.VER. 19956.a, sagittal reconstruction of the copulatory apparatus; anterior to the right; B, CGAS Pla 22.3, sagittal reconstruction of the copulatory apparatus; anterior to the right.
Distribution. Malay Peninsula and N Borneo (Sabah, N Kalimantan, and Gunung Gading National Park in SW Sarawak). Data from Sumatra might be erroneous; specimens previously reported from there were identified as the Hairy-faced Myotis (M. annectans), but both species might not occur there. Data from Sulawesi identified as M. cf. ridleyi requires more detailed studies, and on zoogeographical grounds, they probably represent a different taxon. in Vespertilionidae
Distribution. Malay Peninsula and N Borneo (Sabah, N Kalimantan, and Gunung Gading National Park in SW Sarawak). Data from Sumatra might be erroneous; specimens previously reported from there were identified as the Hairy-faced Myotis (M. annectans), but both species might not occur there. Data from Sulawesi identified as M. cf. ridleyi requires more detailed studies, and on zoogeographical grounds, they probably represent a different taxon.
FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–j Araceae: a–b Anthurium angustifolium. c Anthurium longifolium. d Anthurium pentaphyllum. e Philodendron bernardopazii. f Philodendron hatschbachii. g Philodendron hederaceum. h Philodendron ornatum. i Philodendron pedatum. j Thaumatophyllum corcovadense. k Asplenium auriculatum (Aslpeniaceae). l Begonia solananthera. Bromeliaceae: m Aechmea araneosa. n Aechmea capixabae. o Aechmea castanea. in Augusto Ruschi Biological Reserve vascular epiphytes: a hotspot in the mountains of the Atlantic Forest of Southeastern Brazil
FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–j Araceae: a–b Anthurium angustifolium. c Anthurium longifolium. d Anthurium pentaphyllum. e Philodendron bernardopazii. f Philodendron hatschbachii. g Philodendron hederaceum. h Philodendron ornatum. i Philodendron pedatum. j Thaumatophyllum corcovadense. k Asplenium auriculatum (Aslpeniaceae). l Begonia solananthera. Bromeliaceae: m Aechmea araneosa. n Aechmea capixabae. o Aechmea castanea.
FIGURE. Individuals in four Populations of Sanicula orthacantha, showing the variation in plant size and rhizome character (each line represents a population). A. China, Hubei, Xuan'en, Qizimei Mountain, H.M. Li, Y.M. Yi & Y.S. Zhang 1077 (NAS). B. China, Jiangxi, Jiujiang, Lushan, H.M. Li, Y.S. Zhang & Y. Xu 1109 (NAS). C. China, Chongqing, Nanchuan, Jinfo Shan, H.M. Li, Y.S. Zhang & X. Zhang 1141 (NAS). D. China, Sichuan, Emei Shan, H.M. Li & Y.S. Zhang 1157 (NAS). All same scale. in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Individuals in four Populations of Sanicula orthacantha, showing the variation in plant size and rhizome character (each line represents a population). A. China, Hubei, Xuan'en, Qizimei Mountain, H.M. Li, Y.M. Yi & Y.S. Zhang 1077 (NAS). B. China, Jiangxi, Jiujiang, Lushan, H.M. Li, Y.S. Zhang & Y. Xu 1109 (NAS). C. China, Chongqing, Nanchuan, Jinfo Shan, H.M. Li, Y.S. Zhang & X. Zhang 1141 (NAS). D. China, Sichuan, Emei Shan, H.M. Li & Y.S. Zhang 1157 (NAS). All same scale.
Distribution. Widely distributed in tropical and subtropical waters throughout the world. It is occasionally recorded stranding in temperate waters, but these may represent vagrant individuals. in Ziphiidae
Distribution. Widely distributed in tropical and subtropical waters throughout the world. It is occasionally recorded stranding in temperate waters, but these may represent vagrant individuals.
FIGURE. Phylogenetic tree derived from Bayesian analysis, based on nrITS1-5.8S-ITS2 region data. Posterior probability (PP> 0.95) values from the Bayesian analysis are added at the nodes. The scale bar represents the number of nucleotide changes per site. (T) indicates the type specimen for this species. The new species are in bold. in Four new species of Entoloma (Entolomataceae, Agaricomycetes) subgenera Cyanula and Claudopus from Vietnam and their phylogenetic position
FIGURE. Phylogenetic tree derived from Bayesian analysis, based on nrITS1-5.8S-ITS2 region data. Posterior probability (PP> 0.95) values from the Bayesian analysis are added at the nodes. The scale bar represents the number of nucleotide changes per site. (T) indicates the type specimen for this species. The new species are in bold.
Distribution. NE Pakistan, NW & NE India, Nepal, Myanmar, S China (Yunnan), Thai-land, Laos, Vietnam, and Cambodia. Records from W Sumatra and C & E Java likely represent introduced populations. in Muridae
Distribution. NE Pakistan, NW & NE India, Nepal, Myanmar, S China (Yunnan), Thai-land, Laos, Vietnam, and Cambodia. Records from W Sumatra and C & E Java likely represent introduced populations.
FIGURE 4 in First representatives of the stonefly genus Perlomyia and the beaded lacewing genus Isoscelipteron from the Upper Miocene of France (Plecoptera: Leuctridae and Neuroptera: Berothidae), with biogeographical considerations
FIGURE 4. Perlomyia cantalensis sp. nov., holotype IF-STR-0104. Reconstruction of terminalia.. Scale bar = 1 mm.
FIGURE 3 in First representatives of the stonefly genus Perlomyia and the beaded lacewing genus Isoscelipteron from the Upper Miocene of France (Plecoptera: Leuctridae and Neuroptera: Berothidae), with biogeographical considerations
FIGURE 3. Perlomyia cantalensis sp. nov., holotype IF-STR-0104. Photograph of hind wing. Scale bar = 2 mm.
FIGURE 1 in First representatives of the stonefly genus Perlomyia and the beaded lacewing genus Isoscelipteron from the Upper Miocene of France (Plecoptera: Leuctridae and Neuroptera: Berothidae), with biogeographical considerations
FIGURE 1. Perlomyia cantalensis sp. nov., holotype IF-STR-0104. Photograph of general habitus. Scale bar = 2 mm.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.