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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.
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.
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.
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.
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.
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.
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.
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)
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.
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.
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).
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.
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.
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.
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
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
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
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
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
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
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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)
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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.
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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
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