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131 results for “Kyushu”
FIGURE 5 in A new species of Pseudodiaptomus (Copepoda: Calanoida) from Japan, with notes on the closely related P. inopinus Burckhardt, 1913 from Kyushu Island
FIGURE 5. Pseudodiaptomus nansei sp. nov. Female (A–F, holotype; G, paratype): A–E, legs 1–5, posterior; F, base of third exopodal segment of leg 5, posterior; G, base of third exopodal segment of leg 5, anterior.
FIGURE 1 in A new species of Pseudodiaptomus (Copepoda: Calanoida) from Japan, with notes on the closely related P. inopinus Burckhardt, 1913 from Kyushu Island
FIGURE 1. Map of the Nansei Islands and Kyushu Island. Locations of the rivers (R.) where sampling occurred are indicated by black spots, among which those with the numbers represent the rivers from which specimens of the new species or P. inopinus Burckhardt, 1913 were collected in the Nansei Islands (1, Hirakubo-gawa R.; 2, Miyara-gawa R.; 3, Yakashimoguchi-gawa R.; 4, Tokuhina-gawa R.; 5, Ginozafukuchi-gawa R.; 6, Chinaze-gawa R.; 7, Kawauchi-gawa R.; 8, Yakugachi-gawa R.; 9, Ura-gawa R.) and Kyushu Island (10, Tsuri-kawa R.; 11, Imari-gawa R.; 12, Yukiura-gawa R.; 13, Rokkaku-gawa R.; 14, Chikugo-gawa R.; 15, Manose-gawa R.; 16, Hitotsuse-gawa R.; 17, Shiomi-gawa R.; 18, Yasaka-gawa R.; 19, Yamakuni-gawa R.).
FIGURE 6 in A new species of Pseudodiaptomus (Copepoda: Calanoida) from Japan, with notes on the closely related P. inopinus Burckhardt, 1913 from Kyushu Island
FIGURE 6. Pseudodiaptomus nansei sp. nov. Male (A–F, allotype; G, specimen from Ura-gawa River): A, habitus, dorsal; B, habitus, right lateral; C, second urosomite, ventral; D, right antennule; E, leg 5, posterior; F, leg 5, anterior; G, moderately paddle-shaped second exopodal segment of left leg 5.
FIGURE 6 in New records of callianassid ghost shrimp (Crustacea: Decapoda: Axiidea) from reducing environments in Kyushu, southwestern Japan
FIGURE 6. Nihonotrypaea thermophila Lin, Komai & Chan, 2007, male (cl. 9.6 mm), JAMSTEC No. 2050025167. A, left third maxilliped, lateral view (setae omitted); B, right major cheliped, lateral view; C, tuberculate ridge on fixed finger of right major cheliped, mesial view; D, left minor cheliped, lateral view (proximal part of ischium omitted); E, distal 3 segments of left third pereopod, lateral view. Scale bars: 2 mm.
FIGURE 2. Cheramus cavifrons n in New records of callianassid ghost shrimp (Crustacea: Decapoda: Axiidea) from reducing environments in Kyushu, southwestern Japan
FIGURE 2. Cheramus cavifrons n. sp., holotype, ovigerous female (cl 3.7 mm), NSMT-Cr 22092. A, carapace and cephalic appendages, lateral view; B, anterior part of carapace and cephalic appendages, lateral view; C, rostrum and eyes, dorsal view; D, thoracic shield and coxae of fourth pereopods, ventral view; E, posterior part of cephalothorax and abdomen (left third pleopod removed), lateral view, showing direction of fourth pereopod; F, left first maxilliped, outer view (distal endite broken off); G, left second maxilliped; H, left third pleopod, posterior view (setae omitted); I, same, appendix interna. Scale bars: 1 mm for A–E; 0.5 mm for F–I.
FIGURE 5 in New records of callianassid ghost shrimp (Crustacea: Decapoda: Axiidea) from reducing environments in Kyushu, southwestern Japan
FIGURE 5. Nihonotrypaea thermophila Lin, Komai & Chan, 2007, male (cl. 9.6 mm), JAMSTEC No. 2050025167. A, carapace and cephalic appendages, lateral view; B, anterior part of carapace and cephalic appendages, dorsal view; C, sixth abdominal somite, dorsal view; D, telson and left uropod, dorsal view (setae omitted); E, appendix interna of left third pleopod, ventral view. Scale bars: 2 mm for A–D; 0.5 mm for E.
FIGURE 3. Cheramus cavifrons n in New records of callianassid ghost shrimp (Crustacea: Decapoda: Axiidea) from reducing environments in Kyushu, southwestern Japan
FIGURE 3. Cheramus cavifrons n. sp., holotype, ovigerous female (cl 3.7 mm), NSMT-Cr 22092. A, left major cheliped, lateral view; B, same, mesial view; C, right minor cheliped, lateral view; D, same, mesial view. Scale bar: 1 mm.
FIGURE 1. Cheramus cavifrons n in New records of callianassid ghost shrimp (Crustacea: Decapoda: Axiidea) from reducing environments in Kyushu, southwestern Japan
FIGURE 1. Cheramus cavifrons n. sp., holotype, ovigerous female (cl 3.7 mm), NSMT-Cr 22092. Body parts in dorsal view. A, carapace and cephalic appendages; B, first and second abdominal somites; C, third abdominal somite; D, fourth abdominal somite; E, fifth abdominal somite; F, sixth abdominal somite, telson and right uropod (setae partially omitted). Scale bar: 1 mm.
FIGURE 4. Cheramus cavifrons n in New records of callianassid ghost shrimp (Crustacea: Decapoda: Axiidea) from reducing environments in Kyushu, southwestern Japan
FIGURE 4. Cheramus cavifrons n. sp., holotype, ovigerous female (cl 3.7 mm), NSMT-Cr 22092. A, left third maxilliped, lateral view; B, same mesial view; C, left second pereopod, lateral view; D, left third pereopod, lateral view; E, left fourth pereopod, outer view; F, left fifth pereopod lateral view; G, same, distal 2 segments, extensor view; H, left uropod, perpendicular dorsal view; I, posterior margin of telson. Scale bars: 0.5 mm.
FIGURE 2. A–C in Unusual preservation of fossil mantis shrimp (Stomatopoda): occurrence of mandibles from the Pleistocene Ogushi Formation, Kyushu, Japan
FIGURE 2. A–C, right mandible of Stomatopoda (MFM214701). A, occlusal view. B, anterior view. C, posterior view. D–E, right mandible of Stomatopoda (GCM-IVP3141). D, occlusal view. E, posterior view. F, fragment of stomatopod right mandible, occlusal view (GCM-IVP3142). G, right mandible of extant specimen, Oratosquilla oratoria (de Haan, 1844) (MFM214702), posterior view. H–L, fragments of dactylus of the raptorial claw of Stomatopoda. H, MFM214703. I, GCM-IVP3143. J, GCM-IVP3144. K, MFM214704. L, GCM-IVP3145. All scale bars represent 2 mm.
The dataset for β diversity pattern of megabenthic community on a seamount of Philippine Sea: Implications for conservation planning on the Kyushu-Palau Ridge
Open the record for dataset details and reuse information.
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. m. melampus Wagner, 1841 — Japan (Honshu, Kyushu, Shikoku Is). M. m. coreensis Kuroda & Mori, 1923 — North and South Korea. M. m. tsuensis Thomas, 1897 — Japan (Tsushima I). Introduced on Sado and Hokkaido Is. in Mustelidae
Subspecies and Distribution. M. m. melampus Wagner, 1841 — Japan (Honshu, Kyushu, Shikoku Is). M. m. coreensis Kuroda & Mori, 1923 — North and South Korea. M. m. tsuensis Thomas, 1897 — Japan (Tsushima I). Introduced on Sado and Hokkaido Is.
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.
Subspecies and Distribution. L.b.brachyurusTemminck,1845—PacificsideofSHonshu,Shikoku,Kyushu,andsurroundingIs(Awaji,Shodo,Goto,Amakusa,andShimokoshiki). L.b.angustidensHollister,1912—NHonshuandSonSeaofJapanside. L.b.lyoniKishida,1937—SadoI(offWHonshu,WJapan). L. b. okiensis Thomas, 1906 — Oki Is (off SW Honshu, WJapan). in Leporidae
Subspecies and Distribution. L.b.brachyurusTemminck,1845—PacificsideofSHonshu,Shikoku,Kyushu,andsurroundingIs(Awaji,Shodo,Goto,Amakusa,andShimokoshiki). L.b.angustidensHollister,1912—NHonshuandSonSeaofJapanside. L.b.lyoniKishida,1937—SadoI(offWHonshu,WJapan). L. b. okiensis Thomas, 1906 — Oki Is (off SW Honshu, WJapan).
Distribution. WJapan (W Honshu, Shikoku, Kyushu and adjacentislands of Tsushima, Goto Is, Yakushima, Tanegashima, Oki Is, Yashirojima, Shodoshima, and Awajishima); E limit of distribution on Honshu is located across Ishikawa, Gifu, Nagano, and Shizuoka prefectures. in Talpidae
Distribution. WJapan (W Honshu, Shikoku, Kyushu and adjacentislands of Tsushima, Goto Is, Yakushima, Tanegashima, Oki Is, Yashirojima, Shodoshima, and Awajishima); E limit of distribution on Honshu is located across Ishikawa, Gifu, Nagano, and Shizuoka prefectures.
Distribution. Japan (Honshu, Shikoku, and Kyushu); distribution in C Honshu is rather continuous, while N & W distribution is patchy and isolated due to mountainous topography. in Talpidae
Distribution. Japan (Honshu, Shikoku, and Kyushu); distribution in C Honshu is rather continuous, while N & W distribution is patchy and isolated due to mountainous topography.
Distribution. Originally endemic to Japan, and mainly distributed in Honshu, Shikoku, and Kyushu; it has been found in other small islands including Sado, Oki Is, Mishima, Okinoshima (Fukuoka Prefecture), Tanegashima, Yakushima, Nakanoshima (Tokara Is), and Izu Is. Introduced to Hokkaido and Jeju I (South Korea). in Soricidae
Distribution. Originally endemic to Japan, and mainly distributed in Honshu, Shikoku, and Kyushu; it has been found in other small islands including Sado, Oki Is, Mishima, Okinoshima (Fukuoka Prefecture), Tanegashima, Yakushima, Nakanoshima (Tokara Is), and Izu Is. Introduced to Hokkaido and Jeju I (South Korea).
Distribution. Endemic to Japan, widely distributed on Honshu and Kyushu. No recent records of extant distribution but fossil records found on Shikoku. in Soricidae
Distribution. Endemic to Japan, widely distributed on Honshu and Kyushu. No recent records of extant distribution but fossil records found on Shikoku.
Distribution. Originally distributed throughout the Indo-Malayan Region and S China, including Taiwan, Hainan, and Sri Lanka (only original range shaded in the map). Possible human-mediate introduced range in Maldives, islands of Malaysia, Indonesia, Brunei, Philippines, Japan (Kyushu and Ryukyu Is), Guam, Palau, and New Guinea. Introduced in historical times into East Africa (Egypt, Sudan, Eritrea, Djibouti, Kenya, Rwanda, and Tanzania), Pemba and Zanzibar (Unguja) Is, Madagascar, Comoro Is, Mauritius, Réunion I, and into coastal Arabia (in the vicinity of seaports in Iraq, Kuwait, Bahrain, Saudi Arabia, Yemen, and Oman). in Soricidae
Distribution. Originally distributed throughout the Indo-Malayan Region and S China, including Taiwan, Hainan, and Sri Lanka (only original range shaded in the map). Possible human-mediate introduced range in Maldives, islands of Malaysia, Indonesia, Brunei, Philippines, Japan (Kyushu and Ryukyu Is), Guam, Palau, and New Guinea. Introduced in historical times into East Africa (Egypt, Sudan, Eritrea, Djibouti, Kenya, Rwanda, and Tanzania), Pemba and Zanzibar (Unguja) Is, Madagascar, Comoro Is, Mauritius, Réunion I, and into coastal Arabia (in the vicinity of seaports in Iraq, Kuwait, Bahrain, Saudi Arabia, Yemen, and Oman).
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