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154 results for “mainland Asia”
Distribution. Mainland SE Asia, Philippines, Indonesian Archipelago, New Guinea (including Bismarck Archipelago), Solomon Is, and NE Australia; also on N Nicobar Is in Hipposideridae
Distribution. Mainland SE Asia, Philippines, Indonesian Archipelago, New Guinea (including Bismarck Archipelago), Solomon Is, and NE Australia; also on N Nicobar Is
Distribution. NE India, NE Bangladesh, S China (including Hainan I), mainland SE Asia, Sumatra (including Simeulue, Nias, and Mentawai Is), Borneo, Java, Kangean, Bali, and many offshore Is. in Hipposideridae
Distribution. NE India, NE Bangladesh, S China (including Hainan I), mainland SE Asia, Sumatra (including Simeulue, Nias, and Mentawai Is), Borneo, Java, Kangean, Bali, and many offshore Is.
Subspecies and Distribution. H. a. armiger Hodgson, 1835 -N India, Nepal, Myanmar, C & S China (including Hainan I), and mainland SE Asia except Vietnam. H. a. fujianensis Zhen, 1987-SE China (Fujian). H. a. terasensis Kishida, 1924 —Taiwan I. H. a. traninhensis Bourret, 1942—Vietnam. in Hipposideridae
Subspecies and Distribution. H. a. armiger Hodgson, 1835 -N India, Nepal, Myanmar, C & S China (including Hainan I), and mainland SE Asia except Vietnam. H. a. fujianensis Zhen, 1987-SE China (Fujian). H. a. terasensis Kishida, 1924 —Taiwan I. H. a. traninhensis Bourret, 1942—Vietnam.
Meteorological and Flux Data in Two Rubber Plantations and a Natural Forest in Mainland Southeast Asia
<p>Rubber plantations have rapidly replaced natural forests in Mainland Southeast Asia, yet the relevant impacts on the terrestrial carbon cycle remain uncertain, especially with an increase in drought frequency. Based on the meteorological and flux data from two rubber sites and one natural forest site, our study investigated the rubber ecosystem fluxes in a marginal (drier) plantation and their responses to drought 2015/2016 compared to a local natural forest, and the differences in ecosystem fluxes and their climatic drivers between the marginal plantation and a traditional humid plantation. </p>
Subspecies and Distribution. M.m.muntjakZimmermann,1780—PeninsularMalaysia,Sumatra,Java,Bali,Borneoandseveralassociatedsmallerislands. M.m.annamensisKloss,1928—SLaos,SVietnam,andCambodia. M.m.aureusC.H.Smith,1826—Pakistan,N&CIndia. M.m.curvostylisGray,1872—Myanmar,Thailand. M.m.malabaricusLydekker,1915—SIndiaandSriLanka. M.m.menglalisWang&Groves,1988—SChina(SYunnan);possiblyalsoinneighboringMyanmar,Laos,andVietnam. M.m.montanusRobinson&Kloss,1918—Sumatranhighlands. M.m.nigripesG.Allen,1930—HainanI. M.m.vaginalisBoddaert,1785—Nepal,Bhutan,NEIndia,andBangladesh. M. m. yunnanensis Ma & Wang, 1988 — S China (from C & N Yunnan and S Sichuan to S Fujian & Guangdong). Forms from mainland Asia have been introduced into the Andaman Is. in Cervidae
Subspecies and Distribution. M.m.muntjakZimmermann,1780—PeninsularMalaysia,Sumatra,Java,Bali,Borneoandseveralassociatedsmallerislands. M.m.annamensisKloss,1928—SLaos,SVietnam,andCambodia. M.m.aureusC.H.Smith,1826—Pakistan,N&CIndia. M.m.curvostylisGray,1872—Myanmar,Thailand. M.m.malabaricusLydekker,1915—SIndiaandSriLanka. M.m.menglalisWang&Groves,1988—SChina(SYunnan);possiblyalsoinneighboringMyanmar,Laos,andVietnam. M.m.montanusRobinson&Kloss,1918—Sumatranhighlands. M.m.nigripesG.Allen,1930—HainanI. M.m.vaginalisBoddaert,1785—Nepal,Bhutan,NEIndia,andBangladesh. M. m. yunnanensis Ma & Wang, 1988 — S China (from C & N Yunnan and S Sichuan to S Fujian & Guangdong). Forms from mainland Asia have been introduced into the Andaman Is.
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. 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.
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.
Distribution. Most of India, Nepal, Bang- ladesh, SC & SE China (Sichuan, Yunnan, Guizhou, Guangdong, and Fujian) and mainland SE Asia (Myanmar, Thailand, Laos, Vietnam, and Cambodia), also on Cat Ba I off the coast of N Vietnam. Popu- lation of Taiwan has uncertain origins. Introduced into Kedah and Perlis regions of Malay Peninsula as well as Java. in Muridae
Distribution. Most of India, Nepal, Bang- ladesh, SC & SE China (Sichuan, Yunnan, Guizhou, Guangdong, and Fujian) and mainland SE Asia (Myanmar, Thailand, Laos, Vietnam, and Cambodia), also on Cat Ba I off the coast of N Vietnam. Popu- lation of Taiwan has uncertain origins. Introduced into Kedah and Perlis regions of Malay Peninsula as well as Java.
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003). in Muridae
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003).
FIGURES 1–4 in Description of Cabamofa vietnamensis sp. nov., the second species of Cabamofa in mainland southeast Asia (Diptera: Bibionomorpha: Sciaroidea incertae sedis)
FIGURES 1–4. Cabamofa vietnamensis sp. nov., male holotype. 1: Habitus, lateral (specimen in ethanol after DNA extraction). 2: Wing, dorsal, setae omitted. 3: Base of wing, dorsal, setae omitted. 4: Genitalia, ventral. Scale for 1 and 2, 1.0 mm, for 3, 0.5 mm, and for 4, 0.1 mm. Abbreviations: cerc = cercus, hyp = hypoproct, tgm = tegmen, tg9 = ninth tergite.
FIGURE 6 in Taxonomic diversity of the Hipposideros larvatus species complex (Chiroptera: Hipposideridae) in mainland Asia
FIGURE 6. Bivariate scatter plot for the second and fourth factors of a Principal Component Analysis based on 18 cranial and dental measurements of 206 specimens Hipposideros larvatus sensu lato.
FIGURE 3 in Taxonomic diversity of the Hipposideros larvatus species complex (Chiroptera: Hipposideridae) in mainland Asia
FIGURE 3. Phylogenetic relationships within the Hipposideros "larvatus" species complex based on COI sequences. BI/ML supports are shown at the tree nodes. Only bootstrap supports over 70 are shown; maximum supports are marked with asterisks. The scale indicates genetic distance estimated by the BI. The bootstrap values derived from 1000 replications.
FIGURE 1 in Taxonomic diversity of the Hipposideros larvatus species complex (Chiroptera: Hipposideridae) in mainland Asia
FIGURE 1. Map, showing the distribution of the specimens of Hipposideros larvatus sensu lato. Localities of morphologically studied material are marked small light blue circles; localities for original genetic samples are marked with larger colour circles (coloration corresponds to the clades of tree based on nuclear markers).
FIGURE 5 in Taxonomic diversity of the Hipposideros larvatus species complex (Chiroptera: Hipposideridae) in mainland Asia
FIGURE 5. Bivariate scatter plot for the first two factors of a Principal Component Analysis based on 18 cranial and dental measurements of 206 specimens Hipposideros larvatus sensu lato.
FIGURE 4 in Taxonomic diversity of the Hipposideros larvatus species complex (Chiroptera: Hipposideridae) in mainland Asia
FIGURE 4. Phylogenetic relationships within the Hipposideros "larvatus" species complex based on seven nuclear gene topologies combined by MRP method. BI/ML/MRP supports are shown at the tree nodes. Maximum supports are marked with asterisks.
FIGURE 7 in Taxonomic diversity of the Hipposideros larvatus species complex (Chiroptera: Hipposideridae) in mainland Asia
FIGURE 7. Penial bones (dorsal, lateral, and ventral views) of H. larvatus from Malaysian Peninsula (ZMMU S202995) and H. poutensis from Cao Bang Province of Vietnam (ZMMU S-200882). Scale bar = 1 mm.
FIG. 7 in Variation in the Arrow Loach, Nemacheilus masyae (Cypriniformes: Nemacheilidae), in Mainland Southeast Asia with Description of a New Species
FIG. 7. Color pattern variation in NemacheiluS maSYae. (A) UF 236087, 44.3 mm SL, Gulf of Thailand drainage; (B) UF 236049, 64.3 mm SL, Panang Tak River drainage; (C) UF 191306, 55.8 mm SL, Mae Klong River drainage; (D) preserved UF 188670, 38.5 mm SL, On River drainage.
FIG. 5 in Variation in the Arrow Loach, Nemacheilus masyae (Cypriniformes: Nemacheilidae), in Mainland Southeast Asia with Description of a New Species
FIG. 5. NemacheiluS zonatus: (A) pectoral fin, UF 188447, 24.4 mm SL; (B) suborbital flap, UF 237302, 28.6 mm SL.
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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.
Annotated Behaviour and Observability Dataset (ABODe)
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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.