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zenodo32/100

FIGURE 25 in The type material of spider wasps (Hymenoptera, Pompilidae) deposited in the Federal Scientific Center of the East Asia Terrestrial Biodiversity, Russian Academy of Sciences, Vladivostok, Russia

FIGURE 25. Kuriloagenia ermolenkoi Loktionov & Lelej, 2014, ♂, holotype. A. Labels. B. Habitus, lateral view. C. Head, lateral view. D. Head, dorsal view. E. Head, frontal view. F. Hypopygium and sternum 7, ventral view. G. Genitalia, ventral view. Scale bar: 1.0 mm for B; 0.5 mm for F, G; 0.2 mm for C, D, E. F, G from Loktionov & Lelej 2014.

opennotspecifiedMar 2022View details →
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FIGURE 2 in A new species of Diacheopsis from Russia

FIGURE 2. Diacheopsis cinerea (holotype). A. Peridium, spores (CM). B, C. Capillitium connected to the peridium, spores (CM). D–F. Capillitium, spores (CM). G. Spores on the peridium (SEM). H. Spore (SEM). I. Spore surface ornamentation (SEM). J. Capillitium connected to the peridium, spores (SEM). Scale bars: A–F = 20 μm, G = 4 μm, H = 2 μm, I = 0.4 μm, J = 30 μm.

opennotspecifiedMar 2022View details →
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FIGURE 3 in A new species of Diacheopsis from Russia

FIGURE 3. Maximum likelihood tree illustrating the phylogeny of Diacheopsis cinerea (holotype) with related species in Stemonitidales based on SSU sequences. The evolutionary history was inferred by using the maximum likelihood method and Tamura-Nei model (Tamura & Nei 1993). The tree with the highest log likelihood (-3167.40) is shown. Values on the branches represent a percentage of the 1000 bootstrap replicates, and the bootstrap values over 75% are shown on the tree. There was a total of 644 positions in the final dataset. Echinostelium minutum (ATCC22345) in Echinosteliales was selected as an outgroup taxon. Evolutionary analysis was conducted using MEGA X. Outgroup is indicated in bold and black. The novel taxon is indicated in bold and blue.

opennotspecifiedMar 2022View details →
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FIGURE 1 in A new species of Diacheopsis from Russia

FIGURE 1. Diacheopsis cinerea (holotype). A–D. Sporocarps (DM). E. Basal rings (DM). Scale bars: A–D = 1 mm, E = 2 mm.

opennotspecifiedMar 2022View details →
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Subspecies and Distribution. M. n. nattereriKuhl, 1817 — broadly extended in N, C & E Europe until 60° N and W Turkey. M.n.hoveliD.L.Harrison,1964—SCTurkey,WSyria,Lebanon,Israel,andWJordan. M. n. tschuliensis Kuzyakin, 1935 — Crimea S to Caucasus region. Isolated populations from W Russia, Crete, Cyprus, and Iraq, Iran, and Turkmenistan are not currently assigned to a subspecies. in Vespertilionidae

Subspecies and Distribution. M. n. nattereriKuhl, 1817 — broadly extended in N, C & E Europe until 60° N and W Turkey. M.n.hoveliD.L.Harrison,1964—SCTurkey,WSyria,Lebanon,Israel,andWJordan. M. n. tschuliensis Kuzyakin, 1935 — Crimea S to Caucasus region. Isolated populations from W Russia, Crete, Cyprus, and Iraq, Iran, and Turkmenistan are not currently assigned to a subspecies.

opennotspecifiedOct 2019View details →
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Distribution. Most of Europe and W Asia, from S Fennoscandia, British Is, and Iberian Peninsula E to W Russia (E to Omsk region), the Caucasus, and N Turkey; disrupted distribution in Mediterranean areas. in Vespertilionidae

Distribution. Most of Europe and W Asia, from S Fennoscandia, British Is, and Iberian Peninsula E to W Russia (E to Omsk region), the Caucasus, and N Turkey; disrupted distribution in Mediterranean areas.

opennotspecifiedOct 2019View details →
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Distribution. SE Europe from Albania and Greece (including Crete) N to S Ukraine and S Russia, the Caucasus, Turkey, and N Iran, and through C Asia to W Mongolia, N, E & C China (including Hainan), and the Himalayas; isolated populations in S Croatia and Korea. Specimens collected from SW Syria may representjuvenile Geoffroy's Myotis (M. emarginatus) or a different form, and are not mapped here. in Vespertilionidae

Distribution. SE Europe from Albania and Greece (including Crete) N to S Ukraine and S Russia, the Caucasus, Turkey, and N Iran, and through C Asia to W Mongolia, N, E & C China (including Hainan), and the Himalayas; isolated populations in S Croatia and Korea. Specimens collected from SW Syria may representjuvenile Geoffroy's Myotis (M. emarginatus) or a different form, and are not mapped here.

opennotspecifiedOct 2019View details →
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Distribution. NE Kazakhstan, SC & SE Russia (including Sakhalin I), N Mongolia, NE Cina (Nei Mongol, TE Jilin, and Liaoning), Korean Peninsula (including Jeju I), much ofJapan (Hokkaido, Honshu, Okushiri, and Rishirito Is), and S Kuril Is (Kunashir) in Vespertilionidae

Distribution. NE Kazakhstan, SC & SE Russia (including Sakhalin I), N Mongolia, NE Cina (Nei Mongol, TE Jilin, and Liaoning), Korean Peninsula (including Jeju I), much ofJapan (Hokkaido, Honshu, Okushiri, and Rishirito Is), and S Kuril Is (Kunashir)

opennotspecifiedOct 2019View details →
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Subspecies and Distribution. M.a.alcathoevonHelversen&Heller,2001—patchilythroughalmostallEurope,fromNSpaintoGermany,includingBritain,andEtoSWUkraineandNWTurkey(EThrace);therearealsoecholocationcallsfromSSwedenthatcertainlyrepresentthisspeciesandtheremayalsoberecordsfromLatvia. M. a. circassicus Benda, Gazaryan & Vallo, 2016 — N slopes of Greater Caucasus in Russia and Abkhazia (Georgia); possibly also found in North Ossetia — Alania Republic (Russia), NE Turkey (Artvin and Erzurum provinces), and Azerbaijan. in Vespertilionidae

Subspecies and Distribution. M.a.alcathoevonHelversen&Heller,2001—patchilythroughalmostallEurope,fromNSpaintoGermany,includingBritain,andEtoSWUkraineandNWTurkey(EThrace);therearealsoecholocationcallsfromSSwedenthatcertainlyrepresentthisspeciesandtheremayalsoberecordsfromLatvia. M. a. circassicus Benda, Gazaryan & Vallo, 2016 — N slopes of Greater Caucasus in Russia and Abkhazia (Georgia); possibly also found in North Ossetia — Alania Republic (Russia), NE Turkey (Artvin and Erzurum provinces), and Azerbaijan.

opennotspecifiedOct 2019View details →
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Subspecies and Distribution. M.h.hilgendorfiPeters,1880—muchofJapan,alsoKunashir(SKurilIs). M.h.ogneviKishida&Mori,1931—RussianFarEast(includingSakhalin),NEChina,andKorea(includingJejuI). M.h. sibirica Kastschenko, 1905 — S Russia, in S Siberia, including Republic of Khakassia, Sayan Mts, Lake Baikal area, and Altai Mts, along with NE Kazakhstan and NW Mongolia. in Vespertilionidae

Subspecies and Distribution. M.h.hilgendorfiPeters,1880—muchofJapan,alsoKunashir(SKurilIs). M.h.ogneviKishida&Mori,1931—RussianFarEast(includingSakhalin),NEChina,andKorea(includingJejuI). M.h. sibirica Kastschenko, 1905 — S Russia, in S Siberia, including Republic of Khakassia, Sayan Mts, Lake Baikal area, and Altai Mts, along with NE Kazakhstan and NW Mongolia.

opennotspecifiedOct 2019View details →
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Subspecies and Distribution. E.s.serotinusSchreber,1774—muchofEuropeexceptforSIberianPeninsulaandmostofScandinavia,beingfoundinSBritainandfromN&CIberianPeninsulaEtoextremeSScandinavia,SWEuropeanRussia,Caucasus,andN&ETurkeyalongwithnumerousMediterraneanIs(BalearicIs,Corsica,Sardinia,andSicily),includingIonian(Corfu)andAegeanIs(Samothrace,Lesbos,Skyros,Euboea,Samos,Crete,andRhodes). E.s.mirzadeFilippi,1865—STurkey,WSyria,Lebanon,Israel,andNW,C&SWIran. E. s. turcomanus Eversmann, 1840 — Central Asia in SC Russia, Kazakhstan, Uzbekistan, Turkmenistan, N Iran, Kyrgyzstan, Tajikistan, N Afghanistan, and NW China (Xinjiang). in Vespertilionidae

Subspecies and Distribution. E.s.serotinusSchreber,1774—muchofEuropeexceptforSIberianPeninsulaandmostofScandinavia,beingfoundinSBritainandfromN&CIberianPeninsulaEtoextremeSScandinavia,SWEuropeanRussia,Caucasus,andN&ETurkeyalongwithnumerousMediterraneanIs(BalearicIs,Corsica,Sardinia,andSicily),includingIonian(Corfu)andAegeanIs(Samothrace,Lesbos,Skyros,Euboea,Samos,Crete,andRhodes). E.s.mirzadeFilippi,1865—STurkey,WSyria,Lebanon,Israel,andNW,C&SWIran. E. s. turcomanus Eversmann, 1840 — Central Asia in SC Russia, Kazakhstan, Uzbekistan, Turkmenistan, N Iran, Kyrgyzstan, Tajikistan, N Afghanistan, and NW China (Xinjiang).

opennotspecifiedOct 2019View details →
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Distribution. Most of Europe (from Ireland and Iberian Peninsula E to Russia and W Kazakhstan), Turkey, and Caucasus; also on Mediterranean Is such as Crete or Mallorca. in Vespertilionidae

Distribution. Most of Europe (from Ireland and Iberian Peninsula E to Russia and W Kazakhstan), Turkey, and Caucasus; also on Mediterranean Is such as Crete or Mallorca.

opennotspecifiedOct 2019View details →
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Subspecies and Distribution. N. n. noctula Schreber, 1774 — throughout Europe from Great Britain, France, and Spain E to W Russia, W Kazakhstan, and SW Turkmenistan, including S Scandinavia, Gotland and Oland Is, and Cyprus (Cyprus records somewhat tentatively regarded as this subspecies). Absent throughout much of Iberia and is locally extinct in Portugal. N. n. lebanoticus D. L.. Harrison, 1962 — WC & SW Syria, Lebanon, and NE Israel. N. n. mecklenburzevi Kuzyakin, 1934 — SC & E Kazakhstan, SC Russia, W Uzbekistan, Tajikistan, Kyrgyzstan, and NW China (Xinjiang). The species may be present in N Africa, with two records claimed from Algeria in 1858, but these may represent N. lasiopterus; further sampling is needed. in Vespertilionidae

Subspecies and Distribution. N. n. noctula Schreber, 1774 — throughout Europe from Great Britain, France, and Spain E to W Russia, W Kazakhstan, and SW Turkmenistan, including S Scandinavia, Gotland and Oland Is, and Cyprus (Cyprus records somewhat tentatively regarded as this subspecies). Absent throughout much of Iberia and is locally extinct in Portugal. N. n. lebanoticus D. L.. Harrison, 1962 — WC & SW Syria, Lebanon, and NE Israel. N. n. mecklenburzevi Kuzyakin, 1934 — SC & E Kazakhstan, SC Russia, W Uzbekistan, Tajikistan, Kyrgyzstan, and NW China (Xinjiang). The species may be present in N Africa, with two records claimed from Algeria in 1858, but these may represent N. lasiopterus; further sampling is needed.

opennotspecifiedOct 2019View details →
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FIGURES 1–12 in Morphological variability of stomatocyst 131 Pang & Wang (Chrysophyceae) from a freshwater shallow lake in South Urals, Russia

FIGURES 1–12. Morphological variability of stomatocyst 131 Pang & Wang from the Lake Zhurmankol (SEM). Figs. 1–6. Immature stomatocysts. Note the different stages of hexagonal pattern development. Figs. 7–9. Mature stomatocysts with fully developed hexagonal pattern and high mesh edges. Figs. 10–12. Structure of the pore-collar complex. Note a regular pore surrounded by a planar annulus. Scale bars: 1 μm.

opennotspecifiedMar 2022View details →
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FIGURE 10. Cognateosymtes serraticoxae Labay, 2018 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994

FIGURE 10. Cognateosymtes serraticoxae Labay, 2018, coastal shallow waters off southeastern Sakhalin Island, female, 6.5 mm: a—incisor and molar of left mandible, b—incisor and raker setae of right mandible, c—maxilliped, d—maxilla 1, e—maxilla 2, f—gnathopod 1, g—gnathopod 2; scales: a, b, d, e—0.1 mm, c, f, g—0.5 mm

opennotspecifiedApr 2022View details →
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FIGURE 9 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994

FIGURE 9. Eosymtes magnumoculis sp. nov., paratype, female, 4.8 mm (the shelf of eastern Sakhalin): a—gnathopod 1, b— palm of propodus and dactylus of gnathopod 1, c—gnathopod 2, d—palm of propodus and dactylus of gnathopod 1; paratype, female, 5.2 mm (the shelf of eastern Sakhalin): e—coxal plate 2 with coxal gill and brood plate; paratype, female, 6.3 mm (the shelf of western Kamchatka): f, g—inner side of coxal plate 1; scales: a, c, e—0.5 mm, b, d, f—0.1 mm; g—0.02 mm

opennotspecifiedApr 2022View details →
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FIGURE 6 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994

FIGURE 6. Eosymtes magnumoculis sp. nov., holotype, female: a—gnathopod 2, b—palm of propodus and dactylus of gnathopod 2, c—pereopod 3; d—pereopod 4; scales: a, c, d—1 mm, b—0.1 mm

opennotspecifiedApr 2022View details →
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FIGURE 7 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994

FIGURE 7. Eosymtes magnumoculis sp. nov., holotype, female: a—pereopod 5, b—pereopod 6, c—pereopod 7, d, e, f—epimeral plates 1–3, g—pleopod 2, h—coupling spines of pleopod 3, i, j, k—coupling setae of pleopods 1, 2 and 3; scales: a–g—1 mm, h–k—0.1 mm

opennotspecifiedApr 2022View details →
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FIGURE 8 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994

FIGURE 8. Eosymtes magnumoculis sp. nov., holotype, female: a—uropod 1, b—uropod 2, c—uropod 3, d—telson; paratype, female, 6.3 mm (the shelf of western Kamchatka): e—microstructure of surface; scales: a, b, c—1 mm, d—0.2 mm, e—0.01 mm

opennotspecifiedApr 2022View details →
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FIGURE 5 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994

FIGURE 5. Eosymtes magnumoculis sp. nov., holotype, female: a—maxilla 1, b—maxilla 2, c—maxilliped, d—gnathopod 1, e—palm of propodus and dactylus of gnathopod 1; paratype, female, 5.3 mm: f—lower lips; paratype, female, 6.3 mm: g—incisor and molar of right mandible; scales: d—0.5 mm; c—0.2 mm; a, b, e, f—0.1 mm

opennotspecifiedApr 2022View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

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abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record