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Distribution. Bhutan, China, India, Japan (Hokkaido), North and South Korea, Nepal, Laos, Mongolia, N Myanmar, Russia, Taiwan, and N Thailand. Introduced to several Japanese islands (Honshu, Kyushu & Shikoku Is). in Mustelidae
Distribution. Bhutan, China, India, Japan (Hokkaido), North and South Korea, Nepal, Laos, Mongolia, N Myanmar, Russia, Taiwan, and N Thailand. Introduced to several Japanese islands (Honshu, Kyushu & Shikoku Is).
Subspecies and Distribution. M..l. leucurus Hodgson, 1847 — C, E & S China.. M. l. amurensis Schrenck, 1859 — NE China (Manchuria), Kazakhstan, Mongolia, North and South Korea, and Russia (E of Volga River). in Mustelidae
Subspecies and Distribution. M..l. leucurus Hodgson, 1847 — C, E & S China.. M. l. amurensis Schrenck, 1859 — NE China (Manchuria), Kazakhstan, Mongolia, North and South Korea, and Russia (E of Volga River).
Subspecies and Distribution. M. f. flavigula Boddaert, 1785 — Bangladesh, Bhutan, C, E & S China, India, Nepal, and Pakistan. M. f. borealis Radde, 1862 — NE China, North and South Korea, and Russia. M. f. chrysospila Swinhoe, 1866 — Taiwan. M. f. indochinensis Kloss, 1916 — Cambodia, Laos, Myanmar, Thailand, and Vietnam. M. f. perunsularis Bonhote, 1901 — Borneo, Malay Peninsula, and Sumatra. M. f. robinsoni Pocock, 1936 — Java. in Mustelidae
Subspecies and Distribution. M. f. flavigula Boddaert, 1785 — Bangladesh, Bhutan, C, E & S China, India, Nepal, and Pakistan. M. f. borealis Radde, 1862 — NE China, North and South Korea, and Russia. M. f. chrysospila Swinhoe, 1866 — Taiwan. M. f. indochinensis Kloss, 1916 — Cambodia, Laos, Myanmar, Thailand, and Vietnam. M. f. perunsularis Bonhote, 1901 — Borneo, Malay Peninsula, and Sumatra. M. f. robinsoni Pocock, 1936 — Java.
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest. in Suidae
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest.
Phytoplankton Community Patterns in the Northeastern South China Sea: Implications of intensified Kuroshio intrusion during the 2015/16 El Niño
<p>Phytoplankton Community Patterns in the Northeastern South China Sea:<br> Implications of intensified Kuroshio intrusion during the 2015/16 El Niño</p>
Magnetotelluric array covering the Xuefengshan-Jiuling belt, South China
<p>The MT data files in EDI format belonging to the array covering the Xuefengshan-Jiuling belt, South China</p>
Seismically imaged mantle exhumation in the Southwest Taiwan Basin of the northeastern South China Sea margin
<p>Dataset for submission of Geochemistry, Geophysics, Geosystems.</p>
FIGURE 4 in Notes on two species of Calostoma (Calostomataceae, Boletales) from the south of China
FIGURE 4. Microscopic features of C. sinocinnabarinum (FHMU3739, holotype). a. Basidiospores. b. Exoperidium hyphae. c. Mesoperidium hyphae. d. First layer of stipe hyphae. e. Second layer of stipe hyphae. Bars = 10 μm. Drawings by C. Xu.
FIGURE 2 in Notes on two species of Calostoma (Calostomataceae, Boletales) from the south of China
FIGURE 2. Basidiomata of Calostoma species. a–c Calostoma areolatum (a from FHMU765; b from FHMU2098; c from FHMU2093); d–f Calostoma sinocinnabarinum (d from FHMU1007; e from FHMU3739, holotype; f from FHMU3818). a–e photos by N.K. Zeng; f photo by S.Z. Huang.
FIGURE 4. Lathrobium zhusha. A male sternite VII B male sternite VIII C in New data on the genus Lathrobium Gravenhorst (Coleoptera: Staphylinidae: Paederinae) of Guangxi, South China
FIGURE 4. Lathrobium zhusha. A male sternite VII B male sternite VIII C aedeagus in ventral view D aedeagus in lateral view. Scales: 0.5 mm.
FIGURE 3. Lathrobium jiuwanshanense. A female tergite VIII B female sternite VIII C female tergites IX–X. D male sternite VII E male sternite VIII F in New data on the genus Lathrobium Gravenhorst (Coleoptera: Staphylinidae: Paederinae) of Guangxi, South China
FIGURE 3. Lathrobium jiuwanshanense. A female tergite VIII B female sternite VIII C female tergites IX–X. D male sternite VII E male sternite VIII F aedeagus in ventral view G aedeagus in lateral view. Scales: 0.5 mm.
FIGURE 2. Lathrobium caiyujiei. A female tergite VIII B female sternite VIII C female tergites IX–X. D male sternite VII E male sternite VIII F in New data on the genus Lathrobium Gravenhorst (Coleoptera: Staphylinidae: Paederinae) of Guangxi, South China
FIGURE 2. Lathrobium caiyujiei. A female tergite VIII B female sternite VIII C female tergites IX–X. D male sternite VII E male sternite VIII F aedeagus in ventral view G aedeagus in lateral view. Scales: 0.5 mm.
FIGURE 1 in New data on the genus Lathrobium Gravenhorst (Coleoptera: Staphylinidae: Paederinae) of Guangxi, South China
FIGURE 1. Male habitus of Lathrobium spp., A L. caiyujiei B L. jiuwanshanense C L. zhusha. Scales: 1.0 mm.
FIGURE 3 in Oreocharis hainanensis (Gesneriaceae), a new species from karst regions in Hainan Island, South China
FIGURE 3. Molecular phylogeny of Hainan Oreocharis taxa and 57 Oreocharis species, based on the combined chloroplast gene trnLtrnF and nuclear ribosomal DNA (nrDNA) sequence ITS1/2 data matrices. Posterior probability (PP) and Bootstrap value (BS) are showed above branches (only shown if BS> 50%). Hainan Oreocharis taxa were showed in grey.
FIGURE 1. Oreocharis hainanensis S.J.Ling & M.X in Oreocharis hainanensis (Gesneriaceae), a new species from karst regions in Hainan Island, South China
FIGURE 1. Oreocharis hainanensis S.J.Ling & M.X. Ren sp. nov. A. Habitat; B. habit; C. adaxial leaf surface; D. abaxial leaf surface; E. lateral view of corolla, sepal and calyx; F. face view of corolla; G. opening flower showing stamens and staminode; H. pistil, stamens and staminode; I. capsule; J. fruit pods; K. seeds; L–N. Main floral visitors: L. Braunapis sp.; M. Apis sp.; N. Amegilla sp.; All photos by Shao-Jun Ling.
FIGURE 2. Oreocharis hainanensis S.J.Ling & M.X in Oreocharis hainanensis (Gesneriaceae), a new species from karst regions in Hainan Island, South China
FIGURE 2. Oreocharis hainanensis S.J.Ling & M.X. Ren sp. nov. A. Habit; B. abaxial leaf surface; C. lateral view of corolla, sepal and calyx; D. front view of corolla; E. opening corolla showing stamens and staminode; F. pistil, stamens and staminode; G. capsule; H. seed. (Drawn by Shu-Ping Guan based on the holotype S.J.Ling 2020091701 in HUTB).
Subspecies and Distribution. F. s. silvestris Schreber, 1777 — Europe E to the Carpathian Mts and the River Dnieper N of the Black Sea. F.s. brockmani Pocock, 1944 — Somalia. F. s. cafra Desmarest, 1822 — Zimbabwe, S Mozambique and South Africa. F. s. caucasica Satunin, 1905 — Caucasus Mts and Turkey. F.s. caudata Gray, 1874 — deserts E Caspian Sea to NW China (Xinjiang) and Mongolia. F. s. foxi Pocock, 1944 — Senegal to Lake Chad. F.s. gordoni Harrison, 1968 — Batinah coast of Oman. F.s. grampia G. S. Miller, 1907 — N Scotland. F. s. griselda Thomas, 1926 — Kalahari region to S Angola. F. s. iraki Cheesman, 1920 — Arabian Desert regions. F. s. lybica Forster, 1780 — desert regions of N Africa to Sudan and N Niger. F.s. melland: Schwann, 1904 — SC Africa. F.s. nesterovi Biurla, 1916 — Mesopotamian region to SW Iran. F. s. ocreata Gmelin, 1791 — Ethiopian highlands. F. s. ornata Gray, 1830 — India. Probably W through Iran. F.s. pyrrhus Pocock, 1944 — N Angola and SW Zaire. F. s. sarda Lataste, 1885 — coastal Maghreb region of Morocco and Algeria. F.s. tristrami Pocock, 1944 — Palestine and Red Sea coast of Arabia. F.s. ugandae Schwann, 1904 — E Africa. in Felidae
Subspecies and Distribution. F. s. silvestris Schreber, 1777 — Europe E to the Carpathian Mts and the River Dnieper N of the Black Sea. F.s. brockmani Pocock, 1944 — Somalia. F. s. cafra Desmarest, 1822 — Zimbabwe, S Mozambique and South Africa. F. s. caucasica Satunin, 1905 — Caucasus Mts and Turkey. F.s. caudata Gray, 1874 — deserts E Caspian Sea to NW China (Xinjiang) and Mongolia. F. s. foxi Pocock, 1944 — Senegal to Lake Chad. F.s. gordoni Harrison, 1968 — Batinah coast of Oman. F.s. grampia G. S. Miller, 1907 — N Scotland. F. s. griselda Thomas, 1926 — Kalahari region to S Angola. F. s. iraki Cheesman, 1920 — Arabian Desert regions. F. s. lybica Forster, 1780 — desert regions of N Africa to Sudan and N Niger. F.s. melland: Schwann, 1904 — SC Africa. F.s. nesterovi Biurla, 1916 — Mesopotamian region to SW Iran. F. s. ocreata Gmelin, 1791 — Ethiopian highlands. F. s. ornata Gray, 1830 — India. Probably W through Iran. F.s. pyrrhus Pocock, 1944 — N Angola and SW Zaire. F. s. sarda Lataste, 1885 — coastal Maghreb region of Morocco and Algeria. F.s. tristrami Pocock, 1944 — Palestine and Red Sea coast of Arabia. F.s. ugandae Schwann, 1904 — E Africa.
Impacts of transboundary transport on coastal air quality of south China
<p>observation data for air pollutants from China’s Ministry of Ecology and Environment</p>
FIGURE 2. Prunus yunkaishanensis. A. Habitat. B. Habit. C in Prunus yunkaishanensis (Rosaceae), a new species from Guangdong, South China
FIGURE 2. Prunus yunkaishanensis. A. Habitat. B. Habit. C. Portion of stem, showing its reddish-brown bark with small lenticels. D. Leaves, adaxial view. E. Stipules. F. Leaf nectaries at the base of leaf abaxial surface. G. Part of leaf abaxial surface, showing sparse punctation. H. Flower, showing reflexed petals that are shorter than stamens. I. Raceme, showing stout rachis and bracts persistent during anthesis. J. Flowering branch, showing racemes in axils of extant or fallen leaves. K. Bract, adaxial view. L. Endocarp, showing reticulately rugose surface. M. Fruiting branch with ovoid fruits.
FIGURE 3 in Prunus yunkaishanensis (Rosaceae), a new species from Guangdong, South China
FIGURE 3. Morphological comparison of Prunus phaeosticta, P. fordiana and P. yunkaishanensis. P. phaeosticta (A–C): A. Leaf blade with cuneate base; B. Inflorescence with slender rachis and soon caducous bracts; C. Infructescence with subglobose fruits. P. fordiana (D–F): D. Leaf blade with cuneate base; E. Inflorescence with slender rachis and soon caducous bracts; F. Infructescence with an ellipsoid fruit. P. yunkaishanensis (G–I): G. Leaf blade with rounded or slightly cordate base; H. Inflorescence with stout rachis and bracts persistent during anthesis; I. Infructescence with ovoid fruits. A, C from X.X. Huang et al. 18800 (IBSC 0860099); B from S. P. Ko 54147 (IBSC 0338000); D from Department of Forestry 90687 (IBSC 0315466); E from F.C. How 71653 (IBSC 0315481); F from N. Liu et al. 2662 (IBSC 0315463); G from B.H. Wu & W.Y. Zhao P20201562 (IBSC); H from B.H. Wu & W.Y. Zhao P20201558 (IBSC); I from B.H. Wu & X.Q. Wen P20201635 (IBSC).
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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)
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
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International Brain Laboratory public data
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OpenNeuro
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