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Subspecies and Distribution. D.s.sumatrensisFischer,1814—SumatraandPeninsularMalaysia. D.s.harrissoniGroves,1965—Borneo. D. s. lasiotis Buckland, 1872 — South-east Asia (could be extinct). in Rhinocerotidae
Subspecies and Distribution. D.s.sumatrensisFischer,1814—SumatraandPeninsularMalaysia. D.s.harrissoniGroves,1965—Borneo. D. s. lasiotis Buckland, 1872 — South-east Asia (could be extinct).
Figure 1 in Evidence from mitochondrial genomics supports the lower Mesozoic of South Asia as the time and place of basal divergence of cypriniform fishes (Actinopterygii: Ostariophysi)
Figure 1. Geographical regions of cypriniform fish distribution at the continental scale. The seven region scheme presented here [Africa (Af), South Asia (Sa), East Asia (Ea), Europe (Eu), Siberia (Sb), and western and eastern North America (Wn & En)] is a modification of the conventional Wallace's six region system (Berra, 2001). East Asia, Europe, and Siberia are subdivisions of the Palaearctic region, overlapping with each other. Western and eastern North America are subdivisions of the Nearctic region.
Figure 5. A in Evidence from mitochondrial genomics supports the lower Mesozoic of South Asia as the time and place of basal divergence of cypriniform fishes (Actinopterygii: Ostariophysi)
Figure 5. A reconciled dispersal-vicariance analysis (DIVA; upper) and a simple parsimonious reconstruction (lower) inference of past ranges at the subfamilial level superimposed over divergence time estimates. Open rectangular bars stand for 95% confidence ranges of the divergence time estimates. The scale bar at the bottom represents the geological time scale according to Gradstein, Ogg & Smith (2004). Maps drawn from Smith, Smith & Funnel (1994) indicate onset (220 Mya) and completion (160 Mya) of the Pangaean breakup, and separation of the Indian land mass from Africa (130 Mya), which allowed marine permeation. Arrowheads indicate rifting margins; hatched pattern indicates area of black shale deposits (Olsen, 1997).
Figure 2. The maximum likelihood tree inferred from 14 594 in Evidence from mitochondrial genomics supports the lower Mesozoic of South Asia as the time and place of basal divergence of cypriniform fishes (Actinopterygii: Ostariophysi)
Figure 2. The maximum likelihood tree inferred from 14 594 nucleotide sites of 60 Cypriniformes and six outgroups (lnL = -203 966.535). Numbers at each branch indicate the resampling the estimated log likelihood (RELL) local bootstrap probabilities. Asterisks indicate 100% local bootstrap support. Two major clades of Cyprinidae (A and B) correspond with those presented in Cavender & Coburn (1992).
Tropical montane forest in South Asia: Composition, structure and dieback in relation to soils and topography
<p>We evaluated the composition, structure and dieback of a montane forest in relation to soils and physiography of an important biogeographic region that has been sparsely studied. Our objectives were to: 1. Describe the forest composition and structure; 2. Assess the current extent of dieback; and 3. Relate tree composition, structure, and dieback proneness to edaphic and physiographic measures. We enumerated all live and dead standing plants ≥ 3 cm diameter at breast height (DBH), in thirty 20×15 m<sup>2</sup> over story plots. We measured all regeneration <u><</u> 1m height in subplots, sampled soils and measures of physiography, and visually rated the proportion of crown die-back, and recorded standing dead trees.</p>
Distribution. SE Asia, from NE India (Assam, Meghalaya, and Mizoram) E to C & S China (S Sichuan, Guizhou, E Hubei, N Hunan, Yunnan, Guangxi, and including Hainan I) and S through Burma (= Myanmar) and mainland South-east Asia to Peninsular Malaysia, also on Tarutao I (SW coast of Thailand), and on Aur, Pemanggil, and Tioman Is (E coast of Peninsular Malaysia); possibly present in Bangladesh. Recorded from Sumatra but needsverification. in Hystricidae
Distribution. SE Asia, from NE India (Assam, Meghalaya, and Mizoram) E to C & S China (S Sichuan, Guizhou, E Hubei, N Hunan, Yunnan, Guangxi, and including Hainan I) and S through Burma (= Myanmar) and mainland South-east Asia to Peninsular Malaysia, also on Tarutao I (SW coast of Thailand), and on Aur, Pemanggil, and Tioman Is (E coast of Peninsular Malaysia); possibly present in Bangladesh. Recorded from Sumatra but needsverification.
Subspecies and Distribution. L.t.tolaiPallas,1778—InnerMongolia(=NeiMongol),andGansu(NCChina). L.t.buchariensisOgnev,1922—TajikistanandNEAfghanistan. L.t.cheybaniBaloutch,1978—SWIran(ZagrosMts). L.t.cinnamomeusShamel,1940—SWSichuan,andNYunnan(SCChina). L.t.filchneriMatschie,1908—Shaanxi(CChina). L.t.lehmanniSevertzov,1873—SKazakhstan,Turkmenistan,andextremeN&NEIran,EtoSSiberia,Mongolia,andXinjiang(NWChina). L. t. swinhoei Thomas, 1894 — from Heilongjiang, Jilin, Liaoning, Inner Mongolia S to Hebei, Beijing, Henan, Shaanxi, Shanxi, and Shandong (NE & E China). The Tolai Hare occurs in the steppes E of the Caspian Sea, S to NE & SW Iran, E through the Middle Asian republics to Afghanistan, and from Kazakhstan and S Siberia to Mongolia, S Russian Far East, NW, C & NE China; an isolated population lives in S Iraq and SW Iran. A single specimen in South Asia might extend the distribution of the Tolai Hare as far S as Jammu and Kashmir, N India. in Leporidae
Subspecies and Distribution. L.t.tolaiPallas,1778—InnerMongolia(=NeiMongol),andGansu(NCChina). L.t.buchariensisOgnev,1922—TajikistanandNEAfghanistan. L.t.cheybaniBaloutch,1978—SWIran(ZagrosMts). L.t.cinnamomeusShamel,1940—SWSichuan,andNYunnan(SCChina). L.t.filchneriMatschie,1908—Shaanxi(CChina). L.t.lehmanniSevertzov,1873—SKazakhstan,Turkmenistan,andextremeN&NEIran,EtoSSiberia,Mongolia,andXinjiang(NWChina). L. t. swinhoei Thomas, 1894 — from Heilongjiang, Jilin, Liaoning, Inner Mongolia S to Hebei, Beijing, Henan, Shaanxi, Shanxi, and Shandong (NE & E China). The Tolai Hare occurs in the steppes E of the Caspian Sea, S to NE & SW Iran, E through the Middle Asian republics to Afghanistan, and from Kazakhstan and S Siberia to Mongolia, S Russian Far East, NW, C & NE China; an isolated population lives in S Iraq and SW Iran. A single specimen in South Asia might extend the distribution of the Tolai Hare as far S as Jammu and Kashmir, N India.
Subspecies and Distribution. M.c.coypusMolina,1782—Chilemainland. M.c.bonariensisE.GeoffroySaint-Hilaire,1805—Bolivia,Paraguay,NArgentina,SEBrazil,andUruguay. M.c.melanopsOsgood,1943—ChiloéI(CChile). M. c. santacruzae Hollister, 1914 — Argentina, from the Chaco S to Patagonia. Introduced widely into N South America, S North America, Europe, Central Asia, and East Africa. in Echimyidae
Subspecies and Distribution. M.c.coypusMolina,1782—Chilemainland. M.c.bonariensisE.GeoffroySaint-Hilaire,1805—Bolivia,Paraguay,NArgentina,SEBrazil,andUruguay. M.c.melanopsOsgood,1943—ChiloéI(CChile). M. c. santacruzae Hollister, 1914 — Argentina, from the Chaco S to Patagonia. Introduced widely into N South America, S North America, Europe, Central Asia, and East Africa.
Subspecies and Distribution. T.b.belanger:Wagner,1841—knownfromSMyanmar. T. b. chinensis |. Anderson, 1879 — known from SC China (Yunnan), Thailand, and Vietnam. This species has a vast distribution, spanning from SW & SC China and Nepal S through Bhutan, NE India, NE Bangladesh, and South-east Asia to extreme N Malay Peninsula; also found on Hainan I. Exact distributions of the subspecies accepted here are not known. in Tupaiidae
Subspecies and Distribution. T.b.belanger:Wagner,1841—knownfromSMyanmar. T. b. chinensis |. Anderson, 1879 — known from SC China (Yunnan), Thailand, and Vietnam. This species has a vast distribution, spanning from SW & SC China and Nepal S through Bhutan, NE India, NE Bangladesh, and South-east Asia to extreme N Malay Peninsula; also found on Hainan I. Exact distributions of the subspecies accepted here are not known.
Subspecies and Distribution. P. v. vampyrus Linnaeus, 1758 — Java. P.v. edulis E. Geoffroy Saint-Hilaire, 1810 — Lesser Sunda Is (Timor). P. v. lanensis Mearns, 1905 — Philippines. P.v. natunae K. Andersen, 1908 — Borneo and Natuna Is. P. v. pluton Temminck, 1853 — W Lesser Sunda Is. P. v. sumatrensis Ludeking, 1862 — S mainland SE Asia and Malay Peninsula, Sumatra, Lingga Archipelago, Bangka, and S Mentawai Is (Sipora, North Pagai, and South Pagai). Chinese record from Shaanxi Province likely alien. in Pteropodidae
Subspecies and Distribution. P. v. vampyrus Linnaeus, 1758 — Java. P.v. edulis E. Geoffroy Saint-Hilaire, 1810 — Lesser Sunda Is (Timor). P. v. lanensis Mearns, 1905 — Philippines. P.v. natunae K. Andersen, 1908 — Borneo and Natuna Is. P. v. pluton Temminck, 1853 — W Lesser Sunda Is. P. v. sumatrensis Ludeking, 1862 — S mainland SE Asia and Malay Peninsula, Sumatra, Lingga Archipelago, Bangka, and S Mentawai Is (Sipora, North Pagai, and South Pagai). Chinese record from Shaanxi Province likely alien.
Survey and case studies information in South Asia
<p>Supplementary information from South Asia component of the CLACSO IDRC Research Assessment Project. </p>
Distribution. Widely distributed in South-east Asia (Myanmar, Laos, Thailand, Cambodia, S Vietnam, and Peninsular Malaysia, including offshore islands). Distribution boundary between this species and the Large White-toothed Shrew (C. dracula), especially in Myanmar or whether their distributions overlapped, is not clear. in Soricidae
Distribution. Widely distributed in South-east Asia (Myanmar, Laos, Thailand, Cambodia, S Vietnam, and Peninsular Malaysia, including offshore islands). Distribution boundary between this species and the Large White-toothed Shrew (C. dracula), especially in Myanmar or whether their distributions overlapped, is not clear.
Subspecies and Distribution. S.e.etruscusSavi,1822—EuropeandCaucasus;thissubspeciesprobablyalsoinTurkey(scatteredrecordsinW,N&SC). S.e.bactrianusStroganov,1958—Tajikistan. S.e.madagascariensisCoquerel,1848—Madagascar. S.e.micronyxBlyth,1855—Himalayas. S.e.nanulaStroganov,1941—Uzbekistan. S.e.nudipesBlyth,1855—NEIndia. S. e. perrottetti Duvernoy, 1842 — S India. Also known from Tenerife I, many Mediterranean Is, North Africa, Arabia, Socotra I, and Central and South-east Asia, but subspecies involved not known. in Soricidae
Subspecies and Distribution. S.e.etruscusSavi,1822—EuropeandCaucasus;thissubspeciesprobablyalsoinTurkey(scatteredrecordsinW,N&SC). S.e.bactrianusStroganov,1958—Tajikistan. S.e.madagascariensisCoquerel,1848—Madagascar. S.e.micronyxBlyth,1855—Himalayas. S.e.nanulaStroganov,1941—Uzbekistan. S.e.nudipesBlyth,1855—NEIndia. S. e. perrottetti Duvernoy, 1842 — S India. Also known from Tenerife I, many Mediterranean Is, North Africa, Arabia, Socotra I, and Central and South-east Asia, but subspecies involved not known.
Distribution. Mainland South-east Asia in S Laos (N limit is 16° 23' N), SC Vietnam (N limit is 14° 30' N), and E Cambodia (Ratanakiri and Mondulkiri provinces); most likely the W limitis the Mekong River, but further studies are needed to confirm this. Records in Vietnam N to 16° 37° N are questionable. in Cercopithecidae
Distribution. Mainland South-east Asia in S Laos (N limit is 16° 23' N), SC Vietnam (N limit is 14° 30' N), and E Cambodia (Ratanakiri and Mondulkiri provinces); most likely the W limitis the Mekong River, but further studies are needed to confirm this. Records in Vietnam N to 16° 37° N are questionable.
Distribution. Mainland South-east Asia in S Myanmar, S Thailand, S Laos, Cambodia (W of Mekong River), and the S tip of Vietnam. Range limit of this species to the E might be the Mekong River. in Cercopithecidae
Distribution. Mainland South-east Asia in S Myanmar, S Thailand, S Laos, Cambodia (W of Mekong River), and the S tip of Vietnam. Range limit of this species to the E might be the Mekong River.
Figs 28-34 in Trachyuropodid mites (Acari: Uropodina) from South-East Asia: catalog, new key and description of two new species
Figs 28-34. Schematic illustrations of dorsal aspect of South-East Asian trachyuropodid mites (Scale bars: 100). (28) Arculatatrachys imitans (Berlese, 1905). (29) Leonardiella cistulata (Hirschmann, 1975). (30) Trachyibana sarawakiensis Kontschán, 2015. (31) Bostocktrachys tuberculata (Berlese, 1913). (32) Bostocktrachys micherdzinskii (Hirschmann, 1976). (33) Bostocktrachys surinensis sp. nov. (34) Bostocktrachys thailandica sp. nov.
Figs 15-21 in Trachyuropodid mites (Acari: Uropodina) from South-East Asia: catalog, new key and description of two new species
Figs 15-21. Bostocktrachys thailandica sp. nov., female holotype. (15) Dorsal idiosoma. (16) Ventral idiosoma. (17) Tritosternum. (18) Ventral view of gnathosoma. (19) Epistome. (20) Lateral view of chelicera. (21) Ventral view of palp.
Figs 5-10 in Trachyuropodid mites (Acari: Uropodina) from South-East Asia: catalog, new key and description of two new species
Figs 5-10. Bostocktrachys surinensis sp. nov., female holotype (5-9) and male paratype (10). (5, 10) Intercoxal area. (6) Tritosternum. (7) Ventral view of gnathosoma and palp. (8) Epistome. (9) Lateral view of chelicera.
Figs 11-14 in Trachyuropodid mites (Acari: Uropodina) from South-East Asia: catalog, new key and description of two new species
Figs 11-14. Bostocktrachys surinensis sp. nov., female holotype. (11) Ventral view of leg I. (12) Ventral view of leg II. (13) Ventral view of leg III. (14) Ventral view of leg IV.
Figs 1-4 in Trachyuropodid mites (Acari: Uropodina) from South-East Asia: catalog, new key and description of two new species
Figs 1-4. Bostocktrachys surinensis sp. nov., female holotype. (1) Dorsal idiosoma. (2) Setae on caudal margin and caudal part of dorsal shield. (3) Area posterior and anterior to transversal dorsal furrow. (4) Ventral idiosoma.
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Allen Brain Atlas
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