Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
163
datasets available to search
ShareScore release 0.9.0
Dataset results
163 results for “Central India”
FIGURES 4A–B in Euparatettix dandakaranyensis sp. nov. (Tetrigidae: Tetriginae) — a new pygmy grasshopper species from Central India
FIGURES 4A–B. Distribution map of E. dandakaranyensis sp. nov. A, India; coloured area denotes Chhattisgarh state; B, Bastar district, the sphere mark denotes the distribution of E. dandakaranyensis sp. nov.
FIGURES 1A–C. A, E in Euparatettix dandakaranyensis sp. nov. (Tetrigidae: Tetriginae) — a new pygmy grasshopper species from Central India
FIGURES 1A–C. A, E. dandakaranyensis sp. nov. female, lateral view; B, dorsal view; C, head showing frontal region (ventral view).
FIGURES 3A–H, A, E in Euparatettix dandakaranyensis sp. nov. (Tetrigidae: Tetriginae) — a new pygmy grasshopper species from Central India
FIGURES 3A–H, A, E. dandakaranyensis sp. nov. head showing median carina of vertex (dorsal view); B, E. sikkimensis head showing median carina of vertex; C, E. dandakaranyensis sp. nov. ovipositor showing a large series of teeth; D, E. sikkimensis, ovipositor showing a large series of teeth; E, E. dandakaranyensis sp. nov. tegmenula; F, E. sikkimensis, tegmenula; G, E. dandakaranyensis sp. nov. separate sheet of tegmenula; H, E. sikkimensis sp. nov. separate sheet of tegmenula.
FIGURE 3. A–B in A new pygmy grasshopper species (Tetrigidae: Tetriginae) from Central India
FIGURE 3. A–B. Distribution map of Ergatettix subtruncatus sp. nov. A. India; B. coloured area denotes Durg, Raipur, Bastar district and the circle mark denotes the distribution of Ergatettix subtruncatus sp. nov.
FIGURE 1. A–M in A new pygmy grasshopper species (Tetrigidae: Tetriginae) from Central India
FIGURE 1. A–M. Ergatettix subtruncatus sp. nov. A–K (Female) L–M (Male): A. Body in dorsal view; B. Body in lateral view; C. Antenna; D. Head frontal ridge; E. Tegmen; F. Paranota; G. Fore leg (external view); H. Mid leg (external view); I. Hind leg (external view); J. Pulvilli; K. Ovipositor in lateral view; L. Body in dorsal view; M. Body in lateral view.
FIGURE 2. A–F in A new pygmy grasshopper species (Tetrigidae: Tetriginae) from Central India
FIGURE 2. A–F. Keys characters: A, C, E Ergatettix subtruncatus sp. nov; A. Pronotum in lateral view; C. Frontal ridge; E. Ovipositor in lateral view. B, D, F reference collection Ergatettix callosus; B. Pronotum in lateral view; D. Frontal ridge; F. Ovipositor in lateral view.
FIGURE 4 in The "Mr. and Mrs. Ghat crab", Ghatiana dvirupa sp. nov. (Decapoda: Brachyura: Gecarcinucidae) from the Central Western Ghats of India
FIGURE 4. Ghatiana dvirupa sp. nov.: A–C, paratype male (29.99 × 20.05 mm), ZSI-WRC C.2444; D–F, paratype female (28.67 × 19.07 mm), ZSI-WRC C.2444. A, D, habitus, dorsal view; B, pleonal somites 3–6 and telson; C, dorsal view of left G1; E, pleonal somites 4–6 and telson; F, thoracic sternites showing vulvae. Scale bars = 10 mm (A, D), 5 mm (B, E, F), 1 mm (C).
FIGURE 2 in The "Mr. and Mrs. Ghat crab", Ghatiana dvirupa sp. nov. (Decapoda: Brachyura: Gecarcinucidae) from the Central Western Ghats of India
FIGURE 2. Ghatiana dvirupa sp. nov., holotype male (26.11 × 17.52 mm), ZSI-WRC C.2443. A, habitus, dorsal view; B, frontal view of cephalothorax; C, habitus, ventral view. Scale bars = 10 mm.
FIGURE 3 in The "Mr. and Mrs. Ghat crab", Ghatiana dvirupa sp. nov. (Decapoda: Brachyura: Gecarcinucidae) from the Central Western Ghats of India
FIGURE 3. Ghatiana dvirupa sp. nov., holotype male (26.11 × 17.52 mm), ZSI-WRC C.2443. A, mouth parts exposed; B, left maxilliped 3; C, outer view of major or right chela; D, pleon; E, dorsal view of left G1; F, dorsal view of left G1 ultimate article; G, ventral view of left G1; H, left G2. Scale bars = 5 mm (C, D), 2 mm (A, B), 1 mm (E, G, H), 0.5 mm (F).
FIGURE 5 in The "Mr. and Mrs. Ghat crab", Ghatiana dvirupa sp. nov. (Decapoda: Brachyura: Gecarcinucidae) from the Central Western Ghats of India
FIGURE 5. Ghatiana dvirupa sp. nov., colour in life: A, holotype male, ZSI-WRC C.2443; B, male, ZSI-WRC C.2447; C, paratype female, ZSI-WRC C.2444; D, paratype female, ZSI-WRC C.2446. Habitats of Ghatiana dvirupa sp. nov.: E, general habitat at type locality; F, male, ZSI-WRC C.2447, in crevice of laterite boulder. Ghatiana aurantiaca Pati & Sharma, 2014, colour in life: G, crab in its natural habitat during wet season (31 August 2013); H, crab outside of its habitat during dry season (28 November 2011). Ghatiana rouxi Pati & Thackeray, 2021, colour in life. I, male, ZSI-WRC C.2177; J, male, ZSI-WRC C.2176. Figure G is credited to Satyen Mehta, which is modified from https://www.inaturalist.org/observations/51882255. This figure is available in colour at Zootaxa online.
FIGURE 1 in The "Mr. and Mrs. Ghat crab", Ghatiana dvirupa sp. nov. (Decapoda: Brachyura: Gecarcinucidae) from the Central Western Ghats of India
FIGURE 1. Map showing the distribution of Ghatiana dvirupa sp. nov. A, Western Ghats; B, Kali Tiger Reserve; C, Atle (type locality). This figure is available in colour at Zootaxa online.
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. Pl. azandica]. A. Allen, 1924 — NE Zaire. P. l. bleyenberghi Lonnberg, 1914 — S Zaire, Zambia, and Angola. P. l. kruger: Roberts, 1929 — NW (Kalahari), N, and SE South Africa. P.l. nubica de Blainville, 1843 — NE and E Africa. P.l. persica Meyer, 1826 — from Iraq to C India in the 19" century; now restricted to the Gir Forest, India. P. l. senegalensis Meyer, 1826 — West Africa E to the Central African Republic. in Felidae
Subspecies and Distribution. Pl. azandica]. A. Allen, 1924 — NE Zaire. P. l. bleyenberghi Lonnberg, 1914 — S Zaire, Zambia, and Angola. P. l. kruger: Roberts, 1929 — NW (Kalahari), N, and SE South Africa. P.l. nubica de Blainville, 1843 — NE and E Africa. P.l. persica Meyer, 1826 — from Iraq to C India in the 19" century; now restricted to the Gir Forest, India. P. l. senegalensis Meyer, 1826 — West Africa E to the Central African Republic.
Distribution. India (Uttarakhand, West Bengal, Maharashtra, Kerala, and Tamil Nadu), C Nepal, Sri Lanka (Central and Uva provinces), SC China (SE Tibet [= Xizang], Yunnan, and Guangxi), and NE Myanmar (known only from type locality in Kachin State). in Vespertilionidae
Distribution. India (Uttarakhand, West Bengal, Maharashtra, Kerala, and Tamil Nadu), C Nepal, Sri Lanka (Central and Uva provinces), SC China (SE Tibet [= Xizang], Yunnan, and Guangxi), and NE Myanmar (known only from type locality in Kachin State).
Distribution. Warmer waters ofthe Pacific and Indian oceans in an area ranging from E Africa, S India and Sri Lanka to Galapagos Is, and possibly as far as Central and South America. Exact distribution remains unclear due to the small number of known strandings, and the taxonomic confusion between the Deraniyagala's Beaked Whale and the Ginkgo-toothed Beaked Whale (M. ginkgodens). in Ziphiidae
Distribution. Warmer waters ofthe Pacific and Indian oceans in an area ranging from E Africa, S India and Sri Lanka to Galapagos Is, and possibly as far as Central and South America. Exact distribution remains unclear due to the small number of known strandings, and the taxonomic confusion between the Deraniyagala's Beaked Whale and the Ginkgo-toothed Beaked Whale (M. ginkgodens).
FIGURE 1. Cercidospora navarroi. A in Cercidospora navarroi, a new species of lichenicolous fungus from the Central Himalayan region of India
FIGURE 1. Cercidospora navarroi. A. Thallus and apothecial disc of Rinodina intermedia infected by C. navarroi (scale bar = 1 mm). B. Magnified view of thallus showing perithecia of C. navarroi (scale bar = 1 mm). C. Magnified view of apothecia of R. intermedia, showing perithecia of C. navarroi (scale bar = 1 mm).
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.
Successful conservation translocation: Population dynamics of tiger recovery in Panna Tiger Reserve, Central India
<p>Tiger (<em>Panthera tigris</em>) is an indicator species of ecological health and conservation efforts. Due to excessive poaching, the tiger was locally extinct in Panna Tiger Reserve, central India. Subsequent successful reintroduction efforts have brought the species back from the verge of extinction and have demonstrated the success of conservation translocations in response to such critical situations.</p> <p>To understand the demographic characteristics of the tigers reintroduced to Panna Tiger Reserve, we used an ensemble approach of different sampling techniques and direct observations from a long-term data-set spanning more than 10 years. We evaluated different demographic indicators (population status, growth rate, mean litter size, inter-birth interval, and survival probability).</p> <p>Since reintroduction in 2009, 18 females have recruited 120 cubs from 45 litters. This led to 59 individuals in 2021 with a growth rate of ~26%. The mean litter size was 2.66 (SE 0.1), and the inter-birth interval was 19.16 months (SE 0.5). The high survival rate of the reintroduced population (0.82±0.2) helped to achieve the success of reintroduction. We observed non-constant mortality trajectories for both sexes (higher survival probabilities for females) with a moderately higher risk of death in younger (<1 year) and older (>10 years) individuals.</p> <p>Our results showed the effectiveness of translocation and conservation efforts. The recovered population can be used as a founder for augmentation in other recovering tiger populations. A long-term tiger-centric management plan should be implemented in the area adjacent to Panna Tiger Reserve to conserve and secure the habitat of the entire landscape for the long-term survival of the reintroduced population in a metapopulation framework.</p>
FIGURES 21, 22 in Description of Enterobius (Colobenterobius) emodensis sp. n. (Nematoda: Oxyuridae) collected from Central Himalayan langur, Semnopithecus schistaceus, in Uttarakhand, India
FIGURES 21, 22. Reproductive organs of immature adult females of Enterobius (Colobenterobius) emodensis sp. n. collected from Semnopithecus schistaceus in Chamoli District, Uttarakhand, India. 21. Ventral view (in worm of 2.48 mm long). 22. Right lateral view (in worm of 3.95 mm long).
FIGURES 15–20 in Description of Enterobius (Colobenterobius) emodensis sp. n. (Nematoda: Oxyuridae) collected from Central Himalayan langur, Semnopithecus schistaceus, in Uttarakhand, India
FIGURES 15–20. Fourth-stage larvae of Enterobius (Colobenterobius) emodensis sp. n. collected from Semnopithecus schistaceus in Chamoli, Uttarakhand, India. 15. Cephalic apex of female, apical view. 16. Anterior portion of male, right lateral view. 17. Posterior portion of male, right lateral view. 18. Anterior portion of female, right lateral view. 19. Posterior portion of female, right lateral view. 20. Anterior portion of premolt female, right lateral view.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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
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.