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48 results for “Vittatus”
FIGURE 4 in Sarcocheilichthys vittatus, a new species of gudgeon (Teleostei: Cyprinidae) from the Poyang Lake Basin in Jiangxi Province, South China
FIGURE 4. Lateral view of body in: (a) S. caobangensis (IHB 587721, 62.5 mm SL) from Li-Jiang flowing into Zhu-Jiang basin; (b) S. sinensis (201711015784, 82.5 mm SL) from Lake Dongting, at Leishi Town, Yuanjiang City, Hunan Province; and (c) S. nigripinnis (IHB 201712029529, 80.5 mm SL) from Hai-He basin, at Anyang City, Henan Province. Scale bar = 10 mm.
FIGURE 3 in Sarcocheilichthys vittatus, a new species of gudgeon (Teleostei: Cyprinidae) from the Poyang Lake Basin in Jiangxi Province, South China
FIGURE 3. (a) Freshly captured (lateral view); (b) and (c) kept in formalin preservative 3 days after capture (lateral and dorsal view); S. parvus, IHB 201804018395, 51.4 mm SL, from Qingni Town, Fuzhou, Jiangxi Province, South China. (d) a copy of Nichols' (1943) illustration for holotype of S. parvus; and (e) lateral view of paratype of S. parvus.
FIGURE 2 in Sarcocheilichthys vittatus, a new species of gudgeon (Teleostei: Cyprinidae) from the Poyang Lake Basin in Jiangxi Province, South China
FIGURE 2. Ventral view of oromandibular structures in: (a) S. vittatus, IHB 201804018393, holotype, male, 83.5 mm SL, from Qingni Town, Fuzhou, Jiangxi Province, South China. (b) S. parvus, IHB 201611010342, male, 56.5 mm SL, in Suichuan County, Jiangxi Province. (c) S. nigripinnis IHB 201707011818, female, 64.5 mm SL, from Yichun City, Jiangxi Province. (d) S. caobangensis, IHB 587721, 62.5 mm SL, from Li-Jiang, a tributary flowing into Xi-Jiang of Zhu-Jiang basin, at Guiling City, Guangxi Province. CS= cornified sheath, LL=lower lip, MB= maxillary barbels.
FIGURE 7 in Sarcocheilichthys vittatus, a new species of gudgeon (Teleostei: Cyprinidae) from the Poyang Lake Basin in Jiangxi Province, South China
FIGURE 7. Maximum likelihood (ML) tree inferred from cyt b gene for 11 putative species of Sarcocheilichthys. Numbers at major internal nodes are bootstrap values and Bayesian posterior probability values for ML /BI tree (left: only values≥50 are reported, right: only values≥0.5 are reported). Haplotypes with * were retrieved from GenBank.
FIGURE 6 in Sarcocheilichthys vittatus, a new species of gudgeon (Teleostei: Cyprinidae) from the Poyang Lake Basin in Jiangxi Province, South China
FIGURE 6. Type locality of S. vittatus: clear, slowly-running water with mixed substrates including sand, gravel and boulders.
FIGURE 2 in Rediscovery of the holotype of Tetragonopterus vittatus Castelnau 1855, a senior synonym of Moenkhausia doceana (Steindachner 1887) (Characiformes: Characidae)
FIGURE 2. The original drawing of the holotype of Tetragonopterus vittatus presented in Castelnau (1855).
FIGURE 7. Rhampsinitus vittatus Lawrence 1931, male. A in Notes on Phalangiidae (Arachnida: Opiliones) of southern Africa with description of new species and comments on within-species variation
FIGURE 7. Rhampsinitus vittatus Lawrence 1931, male. A: Body, dorsal view; B: anterior part of body, lateral view; C: penis, left lateral view; D: penis, dorsal view; E: glans, left lateral view.
FIGURE 4. Discriminant function analysis depicting morphological differentiation within the C. vittatus-hansenae group. Close grey circle indicates C. vittatus Group II. Open circle denotes C. hansenae Group I. Closed black circle represents C. hansenae Group II in Re-evaluating the taxonomic status of Chiromantis in Thailand using multiple lines of evidence (Amphibia: Anura: Rhacophoridae)
FIGURE 4. Discriminant function analysis depicting morphological differentiation within the C. vittatus-hansenae group. Close grey circle indicates C. vittatus Group II. Open circle denotes C. hansenae Group I. Closed black circle represents C. hansenae Group II.
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.
On following pages: 168. Matapalo Broad-nosed Bat (Platyrrhinus matapalensis); 169. Recife Broad-nosed Bat (Platyrrhinus recifinus); 170. Guianan Broad-nosed Bat (Platyrrhinus guianensis); 171. Incan Broad-nosed Bat (Platyrrhinus incarum); 172. Slender Broad-nosed Bat (Platyrrhinus angustirostris); 173. Brown-bellied Broad-nosed Bat (Platyrrhinus fusciventris); 174. Alberico's Broad-nosed Bat (Platyrrhinus albericoi); 175. Greater Broad-nosed Bat (Platyrrhinus vittatus); 176. Choco Broad-nosed Bat (Platyrrhinus chocoensis); 177. Thomas's Broad-nosed Bat (Platyrrhinus dorsalis); 178. Buffy Broad-nosed Bat (Platyrrhinus infuscus); 179. Darien Broad-nosed Bat (Platyrrhinus aquilus); 180. Eldorado Broad-nosed Bat (Platyrrhinus aurarius); 181. Ismael''s Broad-nosed Bat (Platyrrhinus ismaeli); 182. Quechuan Broad-nosed Bat (Platyrrhinus masu); 183. Shadowy Broad-nosed Bat (Platyrrhinus umbratus); 184. Western Broad-nosed Bat (Platyrrhinus nitelinea); 185. Velvety Fruit-eating Bat (Enchisthenes harti); 186. Honduran White Bat (Ectophylla alba). in Phyllostomidae
On following pages: 168. Matapalo Broad-nosed Bat (Platyrrhinus matapalensis); 169. Recife Broad-nosed Bat (Platyrrhinus recifinus); 170. Guianan Broad-nosed Bat (Platyrrhinus guianensis); 171. Incan Broad-nosed Bat (Platyrrhinus incarum); 172. Slender Broad-nosed Bat (Platyrrhinus angustirostris); 173. Brown-bellied Broad-nosed Bat (Platyrrhinus fusciventris); 174. Alberico's Broad-nosed Bat (Platyrrhinus albericoi); 175. Greater Broad-nosed Bat (Platyrrhinus vittatus); 176. Choco Broad-nosed Bat (Platyrrhinus chocoensis); 177. Thomas's Broad-nosed Bat (Platyrrhinus dorsalis); 178. Buffy Broad-nosed Bat (Platyrrhinus infuscus); 179. Darien Broad-nosed Bat (Platyrrhinus aquilus); 180. Eldorado Broad-nosed Bat (Platyrrhinus aurarius); 181. Ismael''s Broad-nosed Bat (Platyrrhinus ismaeli); 182. Quechuan Broad-nosed Bat (Platyrrhinus masu); 183. Shadowy Broad-nosed Bat (Platyrrhinus umbratus); 184. Western Broad-nosed Bat (Platyrrhinus nitelinea); 185. Velvety Fruit-eating Bat (Enchisthenes harti); 186. Honduran White Bat (Ectophylla alba).
FIGURE 9. Navigobius vittatus, WAM P.34032-001, 23.0 in Navigobius kaguya, new species of ptereleotrine goby (Teleostei: Gobiidae) from the West Pacific
FIGURE 9. Navigobius vittatus, WAM P.34032-001, 23.0 mm SL, holotype, Brunei Darussalam. Photo by M.V. Erdmann. (Photo previously published in Allen et al. 2015: fig. 1.)
Lectotype of Scirtetellus vittatus Kiritshenko, 1951
Open the record for dataset details and reuse information.
FIGURES 5A–5I in Revision of the Agrilus vittatus species-group (Coleoptera, Buprestidae, Agrilinae)
FIGURES 5A–5I. Aedeagus of Agrilus mounted in DMHF. 5A–5C, 5E, 5I medial lobe (penis) exposed, 5D, 5F, 5H medial lobe (penis) in natural position. 5A, Agrilus acacivorus sp.nov.; 5B, A. albizivorus sp.nov.; 5C, A. babaulti Théry, 1930; 5D, A. monadikos sp.nov.; 5E, A. occultus sp.nov.; 5F, A. occultus sp.nov.; 5G, A. terraereginae Blackburn, 1892; 5H, A. viridicupreus Saunders, 1866; 5I, A. viridifrons Kerremans, 1893.
FIGURES 4A–4F in Revision of the Agrilus vittatus species-group (Coleoptera, Buprestidae, Agrilinae)
FIGURES 4A–4F. Dry preserved aedeagus, habitus and ovipositor mounted in DMHF of Agrilus. Aedeagus. 4A, A. viridicupreus Saunders, 1866; 4B, A. viridifrons Kerremans, 1893; 4D, A. vittatus Deyrolle, 1864; 4E A. yunnanicola Obenberger, 1936. Ovipositor. 4F, A. viridifrons Kerremans, 1893; Habitus and aedeagus of holotype. 4C, A. fulvovittatus Fisher, 1921.
FIGURES 1A–1G in Revision of the Agrilus vittatus species-group (Coleoptera, Buprestidae, Agrilinae)
FIGURES 1A–1G. Habitus of Agrilus. 1A, Agrilus acacivorus sp.nov.; 1B, A. albizivorus sp.nov.; 1C, A. aurigaster Jendek, 2011; 1D, A. aurigaster Jendek, 2011 (lateral view); 1E, A. babaulti Théry, 1930; 1F, A. coco sp.nov.; 1G, A. monadikos sp.nov.
FIGURES 3A–3J in Revision of the Agrilus vittatus species-group (Coleoptera, Buprestidae, Agrilinae)
FIGURES 3A–3J. Dry preserved aedeagus of Agrilus. 3A, Agrilus acacivorus sp.nov.; 3B, A. albizivorus sp.nov.; 3C, A. aurigaster Jendek, 2011; 3D, A. babaulti Théry, 1930; 3E, A. coco sp.nov.; 3F, A. monadikos sp.nov.; 3G, A. occultus sp.nov.; 3H, A. presbys Jendek. 2011; 3I A. striatocollis Kerremans, 1892; 3J, A. terraereginae Blackburn, 1892.
FIGURES 2A–2H in Revision of the Agrilus vittatus species-group (Coleoptera, Buprestidae, Agrilinae)
FIGURES 2A–2H. Habitus of Agrilus. 2A, A. occultus sp.nov.; 2B, A. presbys Jendek. 2011; 2C, A. striatocollis Kerremans, 1892; 2D, A. terraereginae Blackburn, 1892; 2E, A. viridicupreus Saunders, 1866; 2F, A. viridifrons Kerremans, 1893; 2G, A. vittatus Deyrolle, 1864; 2H A. yunnanicola Obenberger, 1936.
Fig. 15 Oxybelis vittatus. FMNH 170133 in Not withering on the evolutionary vine: systematic revision of the Brown Vine Snake (Reptilia: Squamata: Oxybelis) from its northern distribution
Fig. 15 Oxybelis vittatus. FMNH 170133, from the Canal Zone of Panama. a Profile; b crown; c underside of head
FIGURE 4. Syngonanthus vittatus and other morphologically similar Syngonanthus species. A–E. S in Two new and endangered species of Syngonanthus (Eriocaulaceae) from Chapada dos Veadeiros, Goiás, Brazil
FIGURE 4. Syngonanthus vittatus and other morphologically similar Syngonanthus species. A–E. S. vittatus: A. Habit detail showing specimen at flowering; B. Rosette and roots; C. Elliptic sepal of staminate flower; D. Other forms of sepals revealing concave shapes in staminate flowers; E. Three different shapes of sepals in the same staminate flower revealing asymmetry among the sepals. F–I. Comparison among capitula in Syngonanthus species: F. S. arenarius var. heterophyllus; G. S. vittatus; H. S. densifolius var. brachyphyllus; I. S. densifolius var. majus; J–K. Pistillate flower of S. vittatus: J. Flower exhibiting trichomes on sepals; K. Flower with two sepals removed, the remaining sepal with hairs deciduous, showing the glabrous petals; L. Pistillate flower of S. arenarius var. heterophyllus; M–N. Staminate flowers of S. vittatus: M. Young flower; N. Mature flower; O. Staminate flower of S. arenarius var. heterophyllus. Scale bars: C,M= 500 μm. D–E, J–L, N–O= 1 mm. F–I= 2 mm. (Photos by Mauricio T. C. Watanabe).
FIGURE 1 in Phenotypic variation in Heremites vittatus (Olivier, 1804) (Sauria: Scincidae) from Iran and Turkey
FIGURE 1. Sampling localities of all examined specimens from Iran and Turkey. Colors refer to the country specimens (Red refer to Turkish specimens; Blue refer to Iranian specimens). Numbers next to the dots refer to the specimens in Appendix 1.
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