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zenodo32/100

Subspecies and Distribution. N. n. noctula Schreber, 1774 — throughout Europe from Great Britain, France, and Spain E to W Russia, W Kazakhstan, and SW Turkmenistan, including S Scandinavia, Gotland and Oland Is, and Cyprus (Cyprus records somewhat tentatively regarded as this subspecies). Absent throughout much of Iberia and is locally extinct in Portugal. N. n. lebanoticus D. L.. Harrison, 1962 — WC & SW Syria, Lebanon, and NE Israel. N. n. mecklenburzevi Kuzyakin, 1934 — SC & E Kazakhstan, SC Russia, W Uzbekistan, Tajikistan, Kyrgyzstan, and NW China (Xinjiang). The species may be present in N Africa, with two records claimed from Algeria in 1858, but these may represent N. lasiopterus; further sampling is needed. in Vespertilionidae

Subspecies and Distribution. N. n. noctula Schreber, 1774 — throughout Europe from Great Britain, France, and Spain E to W Russia, W Kazakhstan, and SW Turkmenistan, including S Scandinavia, Gotland and Oland Is, and Cyprus (Cyprus records somewhat tentatively regarded as this subspecies). Absent throughout much of Iberia and is locally extinct in Portugal. N. n. lebanoticus D. L.. Harrison, 1962 — WC & SW Syria, Lebanon, and NE Israel. N. n. mecklenburzevi Kuzyakin, 1934 — SC & E Kazakhstan, SC Russia, W Uzbekistan, Tajikistan, Kyrgyzstan, and NW China (Xinjiang). The species may be present in N Africa, with two records claimed from Algeria in 1858, but these may represent N. lasiopterus; further sampling is needed.

opennotspecifiedOct 2019View details →
zenodo32/100

Distribution. Recorded from three localities in W & C Ethiopia (Beko River, Yamboshi River, and Chercher Mts) and three localities in W Kenya (Marsabit Lake, Mt Gargues, and Ngong); there is an apparent record from Tana Lake in NW Ethiopia, but it does not seem to represent this species (most likely P. hesperidus hesperidus). in Vespertilionidae

Distribution. Recorded from three localities in W & C Ethiopia (Beko River, Yamboshi River, and Chercher Mts) and three localities in W Kenya (Marsabit Lake, Mt Gargues, and Ngong); there is an apparent record from Tana Lake in NW Ethiopia, but it does not seem to represent this species (most likely P. hesperidus hesperidus).

opennotspecifiedOct 2019View details →
zenodo32/100

Subspecies and Distribution. N.p.plancyiGerbe,1880—NE&ECChina(Gansu,Shaanxi,Shanxi,Henan,Beijing,Shandong,Liaoning,andJilin). N.p.labiatusHodgson,1835—HimalayasfromNPakistan,NIndia,Nepal,SCChina,andNMyanmaralongwithNW&SVietnam;mayoccurinThailand,NLaos,NEVietnam,andPeninsularMalaysia,buttherearenoconfirmedrecordsfromtheseregions. N. p. velutinus G. M. Allen, 1923 — C & SE China (Sichuan, Yunnan, Hubei, Anhui, Jiangsu, Shanghai, Zhejiang, Guizhou, Guangxi, Hunan, Jiangxi, Fujian, Guangdong, and Hong Kong) and Taiwan I. The subspecific status of recently collected specimens from the Central Cordillera of Luzon I in the Philippines is uncertain, although they may represent velutinus. Another specimen recently collected from Hainan I may also represent velutinus. in Vespertilionidae

Subspecies and Distribution. N.p.plancyiGerbe,1880—NE&ECChina(Gansu,Shaanxi,Shanxi,Henan,Beijing,Shandong,Liaoning,andJilin). N.p.labiatusHodgson,1835—HimalayasfromNPakistan,NIndia,Nepal,SCChina,andNMyanmaralongwithNW&SVietnam;mayoccurinThailand,NLaos,NEVietnam,andPeninsularMalaysia,buttherearenoconfirmedrecordsfromtheseregions. N. p. velutinus G. M. Allen, 1923 — C & SE China (Sichuan, Yunnan, Hubei, Anhui, Jiangsu, Shanghai, Zhejiang, Guizhou, Guangxi, Hunan, Jiangxi, Fujian, Guangdong, and Hong Kong) and Taiwan I. The subspecific status of recently collected specimens from the Central Cordillera of Luzon I in the Philippines is uncertain, although they may represent velutinus. Another specimen recently collected from Hainan I may also represent velutinus.

opennotspecifiedOct 2019View details →
zenodo32/100

Distribution. Known only confidently from holotype in NE part of N Peninsula of Sulawesi; there are apparently records from Tolai and Rurukan, N Sulawesi, and two other specimens from Tobelo, N Sulawesi, which are all located near type locality, but all of these specimens need to be reexamined to determine whether or not they truly represent this species. in Vespertilionidae

Distribution. Known only confidently from holotype in NE part of N Peninsula of Sulawesi; there are apparently records from Tolai and Rurukan, N Sulawesi, and two other specimens from Tobelo, N Sulawesi, which are all located near type locality, but all of these specimens need to be reexamined to determine whether or not they truly represent this species.

opennotspecifiedOct 2019View details →
zenodo32/100

Subspecies and Distribution. A.p.phaeotisG.S.Miller,1902—E&SEMexico(fromVeracruztoYucatanPeninsula),NGuatemala,Belize,Honduras,ENicaragua,ECostaRica,PanamaandWColombia. A.p.nanusK.Andersen,1906—W&SWMexico(fromSinaloatoOaxaca). A. p. palatinus W. B. Davis, 1970 — S Mexico (SW Chiapas), S Guatemala, W El Salvador, W Nicaragua, and W Costa Rica. Records from W Ecuador and N Peru are unverified; they could represent the Little Fruit-eating Bat (A. ravus), which was thought to be part of this taxon. Those from Venezuela, N Brazil, and Guyana probably represent misidentifications. in Phyllostomidae

Subspecies and Distribution. A.p.phaeotisG.S.Miller,1902—E&SEMexico(fromVeracruztoYucatanPeninsula),NGuatemala,Belize,Honduras,ENicaragua,ECostaRica,PanamaandWColombia. A.p.nanusK.Andersen,1906—W&SWMexico(fromSinaloatoOaxaca). A. p. palatinus W. B. Davis, 1970 — S Mexico (SW Chiapas), S Guatemala, W El Salvador, W Nicaragua, and W Costa Rica. Records from W Ecuador and N Peru are unverified; they could represent the Little Fruit-eating Bat (A. ravus), which was thought to be part of this taxon. Those from Venezuela, N Brazil, and Guyana probably represent misidentifications.

opennotspecifiedOct 2019View details →
zenodo32/100

Subspecies and Distribution. P.p.poeyiGundlach,1861—Cuba,includingIsladelaJuventud. P. p. obtusa G. S. Miller, 1929 — Hispaniola. A record of two individuals captured in the Florida Keys, USA could represent vagrant individuals. in Phyllostomidae

Subspecies and Distribution. P.p.poeyiGundlach,1861—Cuba,includingIsladelaJuventud. P. p. obtusa G. S. Miller, 1929 — Hispaniola. A record of two individuals captured in the Florida Keys, USA could represent vagrant individuals.

opennotspecifiedOct 2019View details →
zenodo32/100

Small set of representative NCLDV genomes

<p>This is a small set of protein prediction files from a variety of giant virus genomes. These can be used to generate phylogenies for the phylogenetic placement of new genomes.</p>

opencc-by-4.0Apr 2022View details →
dryad32/100

Data on the Weather and Habitat and Representative results of qPCR and PCR

<p>We used weather and habitat characteristics, which collected from studied 49 sampling sites, to know how those affect ranavirus infection rate in amphibian larvae of Dryophytes japonicus (Japanese tree frog), Pelophylax nigromaculatus (Black-spotted pond frog), and Lithobates catesbeianus (American bullfrog) in South Korea.</p> <p>Description on the method section: To investigate the relationship between the ranavirus infection rate and habitat characteristics, we analyzed 16 habitat characteristics at each sampling location. The land cover rate (urban area, agricultural area, forest area, grass area, wetland area, bare area, hydrosphere area) within a radius of 3 km2 from the mid-sampling point was calculated on the 2020 South Korean land cover map(http://egis.me.go.kr ). From the land cover data, greenhouse cultivation areas within agricultural areas, salt fields and tidal flat areas within wetland areas, and sea areas within hydrosphere areas were excluded during data handling because these areas are inhabitable for amphibians. Additionally, the shortest distance from the mid-sampling point to agricultural land, mountains, water bodies, and urban areas was calculated in units of 1 m. When a sampling point was located within a specific coverage area, the distance was set to 2 m. All land cover rates, distance data, and altitude values of each sampling point were calculated using QGIS (ver. 3.4.7, QGIS.org 2021). Furthermore, the average air temperature, lowest air temperature, highest air temperature, and average precipitation for the immediately preceding quarter, based on the sampling date of the tadpoles used in the qPCR experiment, were obtained from the local meteorological station closest to the sampling point.</p> <p>We also provided the igures of representative positive qPCR results of D. japonicus (A, B) collected at Haenam, P. nigromaculatus (C, D) collected at Pohang, and L. catesbeianus (E, F) collected at Gmchoen, which showing positive ranavirus detection from the samples, and the Photographs of representative gel electrophoresis of the MCP fragment (~500bp), which confirmed the qPCR result again by sequencing the fragment (G, H) in the further study.</p>

opencc-zeroApr 2022View details →
zenodo32/100

Subspecies and Distribution. R.t.timorensisdeBlainville,1822—TimorI. R.t.djongaVanBemmel,1949-MunaandButonIs. R.t.flovesiensisHeude,1897—Flores1. R.t.macassaricaHeude,1896—Sulawesi. R.t.moluccensisQuoy&Gaimard,1830—MoluccanIs. R.t.renschiSody,1932—Bali. R. t. russa Muller & Schlegel, 1845 — Java. Possibly it is native only to Java and Bali islands, introduced into Lombok, Flores, Sumbawa, Sumba, Timor, Sulawesi, and Moluccan Islands in ancient times. It was introduced during the last centuries in many locations, including New Guinea, Aru Islands, New Britain Is, Australia, New Zealand, New Caledonia, Mauritius, and Comoro Is. The map represents the native range and the oldest introductions. in Cervidae

Subspecies and Distribution. R.t.timorensisdeBlainville,1822—TimorI. R.t.djongaVanBemmel,1949-MunaandButonIs. R.t.flovesiensisHeude,1897—Flores1. R.t.macassaricaHeude,1896—Sulawesi. R.t.moluccensisQuoy&amp;Gaimard,1830—MoluccanIs. R.t.renschiSody,1932—Bali. R. t. russa Muller &amp; Schlegel, 1845 — Java. Possibly it is native only to Java and Bali islands, introduced into Lombok, Flores, Sumbawa, Sumba, Timor, Sulawesi, and Moluccan Islands in ancient times. It was introduced during the last centuries in many locations, including New Guinea, Aru Islands, New Britain Is, Australia, New Zealand, New Caledonia, Mauritius, and Comoro Is. The map represents the native range and the oldest introductions.

opennotspecifiedAug 2011View details →
zenodo32/100

FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–o Orchidaceae: a Maxillaria milenae. b Maxillaria nasuta. c Maxillaria notylioglossa. d Maxillaria ochroleuca. e Maxillaria rigida. f Myoxanthus punctatus. g Myoxanthus ruschii. h Octomeria alexandri. i Octomeria crassifolia. j. Octomeria gracilis. k Octomeria juncifolia. l Octomeria rotundiglossa. m Pabstiella lingua. n Pabstiella lueriana. o Pabstiella matinhensis. 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–o Orchidaceae: a Maxillaria milenae. b Maxillaria nasuta. c Maxillaria notylioglossa. d Maxillaria ochroleuca. e Maxillaria rigida. f Myoxanthus punctatus. g Myoxanthus ruschii. h Octomeria alexandri. i Octomeria crassifolia. j. Octomeria gracilis. k Octomeria juncifolia. l Octomeria rotundiglossa. m Pabstiella lingua. n Pabstiella lueriana. o Pabstiella matinhensis.

opennotspecifiedMay 2022View details →
zenodo32/100

FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–o Orchidaceae: a Barbosella gardneri. b Bifrenaria clavigera. c Bifrenaria mellicolor. d Campylocentrum ornithorrhynchum. e Cattleya harpophylla. f Cirrhaea nasuta. g Comparettia coccinea. h Crocodeilanthe spiralis. i Dichaea cogniauxiana. j Elleanthus linifolius. k Encyclia patens. l Epidendrum armeniacum. m Epidendrum carpophorum. n Epidendrum henschenii. o Epidendrum proligerum. 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–o Orchidaceae: a Barbosella gardneri. b Bifrenaria clavigera. c Bifrenaria mellicolor. d Campylocentrum ornithorrhynchum. e Cattleya harpophylla. f Cirrhaea nasuta. g Comparettia coccinea. h Crocodeilanthe spiralis. i Dichaea cogniauxiana. j Elleanthus linifolius. k Encyclia patens. l Epidendrum armeniacum. m Epidendrum carpophorum. n Epidendrum henschenii. o Epidendrum proligerum.

opennotspecifiedMay 2022View details →
zenodo32/100

FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–c Hymenophyllaceae: a Hymenophyllum polyanthos. b Polyphlebium angustatum. c Trichomanes polypodioides. d Phlegmariurus martii (Lycopodiaceae). e–o Orchidaceae: e Acianthera auriculata. f Acianthera glanduligera. g Acianthera nemorosa. h Acianthera parahybunensis. i Acianthera ramosa. j Acianthera tricarinata. k Anathallis adenochila. l Anathallis aristulata. m Anathallis linearifolia. n Anathallis microphyta. o Anathallis sclerophylla. 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–c Hymenophyllaceae: a Hymenophyllum polyanthos. b Polyphlebium angustatum. c Trichomanes polypodioides. d Phlegmariurus martii (Lycopodiaceae). e–o Orchidaceae: e Acianthera auriculata. f Acianthera glanduligera. g Acianthera nemorosa. h Acianthera parahybunensis. i Acianthera ramosa. j Acianthera tricarinata. k Anathallis adenochila. l Anathallis aristulata. m Anathallis linearifolia. n Anathallis microphyta. o Anathallis sclerophylla.

opennotspecifiedMay 2022View details →
zenodo32/100

FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–g Bromeliaceae: a Vriesea poenulata. b Vriesea pulchra. c Vriesea racinae. d Vriesea rhodostachys. e Vriesea simplex. f Vriesea tijucana. g Vriesea vagans. h Thoracocarpus bissectus (Cyclanthaceae). i–j Dryopteridaceae: i Elaphoglossum luridum. j Elaphoglossum plumosum. k–n Gesneriaceae: k Codonanthe devosiana. l Nematanthus albus. m Nematanthus crassifolius. n Nematanthus kautskyi. o Hymenophyllum caudiculatum (Hymenophyllaceae). 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–g Bromeliaceae: a Vriesea poenulata. b Vriesea pulchra. c Vriesea racinae. d Vriesea rhodostachys. e Vriesea simplex. f Vriesea tijucana. g Vriesea vagans. h Thoracocarpus bissectus (Cyclanthaceae). i–j Dryopteridaceae: i Elaphoglossum luridum. j Elaphoglossum plumosum. k–n Gesneriaceae: k Codonanthe devosiana. l Nematanthus albus. m Nematanthus crassifolius. n Nematanthus kautskyi. o Hymenophyllum caudiculatum (Hymenophyllaceae).

opennotspecifiedMay 2022View details →
zenodo32/100

FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–o Bromeliaceae: a Aechmea lamarchei. b Aechmea pineliana. c Billbergia euphemiae. d Billbergia lymanii. e Billbergia vittata. f Neoregelia guttata. g Nidularium cariacicaense. h Nidularium longiflorum. i Nidularium procerum. j Portea fosteriana. k Quesnelia strobilispica. l Tillandsia kautskyi. m Vriesea breviscapa. n Vriesea ensiformis. o Vriesea longicaulis. 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–o Bromeliaceae: a Aechmea lamarchei. b Aechmea pineliana. c Billbergia euphemiae. d Billbergia lymanii. e Billbergia vittata. f Neoregelia guttata. g Nidularium cariacicaense. h Nidularium longiflorum. i Nidularium procerum. j Portea fosteriana. k Quesnelia strobilispica. l Tillandsia kautskyi. m Vriesea breviscapa. n Vriesea ensiformis. o Vriesea longicaulis.

opennotspecifiedMay 2022View details →
zenodo32/100

FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–o Orchidaceae: a Epidendrum ramosum. b Epidendrum saxatile. c Epidendrum vesicatum. d Gomesa jucunda. e Gomesa polyodonta. f Gomesa ranifera. g Gomesa recurva. h Grandiphyllum auricula. i Grandiphyllum edwallii. j Leptotes tenuis. k Masdevallia infracta. l Maxillaria brasiliensis. m Maxillaria desvauxiana. n Maxillaria imbricata. o Maxillaria kautskyi. 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–o Orchidaceae: a Epidendrum ramosum. b Epidendrum saxatile. c Epidendrum vesicatum. d Gomesa jucunda. e Gomesa polyodonta. f Gomesa ranifera. g Gomesa recurva. h Grandiphyllum auricula. i Grandiphyllum edwallii. j Leptotes tenuis. k Masdevallia infracta. l Maxillaria brasiliensis. m Maxillaria desvauxiana. n Maxillaria imbricata. o Maxillaria kautskyi.

opennotspecifiedMay 2022View details →
zenodo32/100

FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–o Orchidaceae: a Pabstiella nymphalis. b Pabstiella pterophora. c Pabstiella seriata. d Pabstiella trifida. e Pabstiella villosisepala. f Phloeophila numularia. g Promenaea stapelioides. h Proschechea kautskyi. i Prosthechea pachysepala. j Scuticaria hadwenii. k Specklinia marginalis. l Specklinia subpicta. m Stelis aprica. n Stelis argentata. o Stelis intermedia. 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–o Orchidaceae: a Pabstiella nymphalis. b Pabstiella pterophora. c Pabstiella seriata. d Pabstiella trifida. e Pabstiella villosisepala. f Phloeophila numularia. g Promenaea stapelioides. h Proschechea kautskyi. i Prosthechea pachysepala. j Scuticaria hadwenii. k Specklinia marginalis. l Specklinia subpicta. m Stelis aprica. n Stelis argentata. o Stelis intermedia.

opennotspecifiedMay 2022View details →
zenodo32/100

FIGURE 2 in The youngest and first Lebanese representative of the family Saucrosmylidae (Insecta, Neuroptera) from the Cenomanian

FIGURE 2. Lebanosmylus leae gen. et sp. nov., holotype, wing counterpart. A, Photograph. B, Photograph with inverted colors. C, Line drawing. Scale bars = 10 mm.

opennotspecifiedApr 2022View details →
zenodo32/100

FIGURE 1 in The youngest and first Lebanese representative of the family Saucrosmylidae (Insecta, Neuroptera) from the Cenomanian

FIGURE 1. Lebanosmylus leae gen. et sp. nov., holotype, wing. A, Photograph. B, Photograph with inverted colors. C, Line drawing, terminology of venation after Liu et al. (2013). Scale bars = 10 mm.

opennotspecifiedApr 2022View details →
zenodo32/100

FIGURE 1 in A new fossil representative of the scorpionfly subfamily Panorpinae (Mecoptera, Panorpidae) from the Miocene of France

FIGURE 1. Panorpa sp., specimen IGR-PAL-3000. A, Photograph of wing. B, Interpretative line drawing of wing venation with names of main veins labeled. Scale bars = 2 mm.

opennotspecifiedApr 2022View details →
zenodo32/100

FIGURE 1. Representative Palaeocene insects from the Sanshui Basin. A–D in A brief report on the Palaeocene insects from the Sanshui Basin of Guangdong, South China

FIGURE 1. Representative Palaeocene insects from the Sanshui Basin. A–D, Orthoptera (Grylloidea). E–F, Blattodea.

opennotspecifiedApr 2022View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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