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.
3,853
datasets available to search
ShareScore release 0.7.1
Dataset results
3,853 results for “russia”
Fig. 6 in Osteology and relationships of Olorotitan arharensis, a hollow-crested hadrosaurid dinosaur from the latest Cretaceous of Far Eastern Russia
Fig. 6. Right maxilla of hadrosaurid dinosaur Olorotitan arharensis Godefroit, Bolotsky, and Alifanov, 2003 (AEHM 2/845, holotype), from the Upper Cretaceous of Kundur (Russia), in lateral (A) and medial (B) views. Photographs (A1, B1), explanatory drawings (A2, B2).
Fig. 13. Axis complex and cervical vertebrae 3–4 in Osteology and relationships of Olorotitan arharensis, a hollow-crested hadrosaurid dinosaur from the latest Cretaceous of Far Eastern Russia
Fig. 13. Axis complex and cervical vertebrae 3–4 of hadrosaurid dinosaur Olorotitan arharensis Godefroit, Bolotsky, and Alifanov 2003 (AEHM 2/845, holotype), from the Upper Cretaceous of Kundur (Russia), in right lateral (A) and dorsal (B) views. Abbreviatons: ax, axis; cv, cervical vertebra.
Fig. 2 in Osteology and relationships of Olorotitan arharensis, a hollow-crested hadrosaurid dinosaur from the latest Cretaceous of Far Eastern Russia
Fig. 2. Holotype (AEHM 2/845) of hadrosaurid dinosaur Olorotitan arharensis Godefroit, Bolotsky, and Alifanov, 2003, from the Upper Cretaceous of Kundur (Russia), as discovered in the field (N49°04'57.5", E130°51'34.1"). Abbreviations: L, left; N, North; R, right.
Fig. 7 in Osteology and relationships of Olorotitan arharensis, a hollow-crested hadrosaurid dinosaur from the latest Cretaceous of Far Eastern Russia
Fig. 7. Right jugal of hadrosaurid dinosaur Olorotitan arharensis Godefroit, Bolotsky, and Alifanov, 2003 (AEHM 2/845, holotype), from the Upper Cretaceous of Kundur (Russia), in lateral (A) and medial (B) views.
Fig. 3 in Osteology and relationships of Olorotitan arharensis, a hollow-crested hadrosaurid dinosaur from the latest Cretaceous of Far Eastern Russia
Fig. 3. Reconstruction of the skull of hadrosaurid dinosaur Olorotitan arharensis Godefroit, Bolotsky, and Alifanov, 2003, from the Upper Cretaceous of Kundur (Russia), in right lateral view.
Fig. 19 in Osteology and relationships of Olorotitan arharensis, a hollow-crested hadrosaurid dinosaur from the latest Cretaceous of Far Eastern Russia
Fig. 19. Hadrosaurid dinosaur Olorotitan arharensis Godefroit, Bolotsky, and Alifanov, 2003 (AEHM 2/845, holotype), from the Upper Cretaceous of Kundur (Russia). A. Left humerus, in cranial (A1), caudal (A2), and lateral (A3) views. B. Right ulna, in cranial (B1) and medial (B2) views. C. Right radius, in caudal (C1) and cranial (C2) views.
Fig. 5 in Osteology and relationships of Olorotitan arharensis, a hollow-crested hadrosaurid dinosaur from the latest Cretaceous of Far Eastern Russia
Fig. 5. Photographs of the braincase of hadrosaurid dinosaur Olorotitan arharensis Godefroit, Bolotsky, and Alifanov, 2003 (AEHM 2/845, holotype), from the Upper Cretaceous of Kundur (Russia), in right lateral (A), left lateral (B), and dorsal (C) views. D. Details of the right lateral view of the braincase.
Fig. 11 in Osteology and relationships of Olorotitan arharensis, a hollow-crested hadrosaurid dinosaur from the latest Cretaceous of Far Eastern Russia
Fig. 11. Right dentary teeth of hadrosaurid dinosaur Olorotitan arharensis Godefroit, Bolotsky, and Alifanov, 2003 (AEHM 2/845, holotype), from the Upper Cretaceous of Kundur (Russia), in lingual views. A. From the middle part of the dental battery. B. From the caudal part of the dental battery.
Fig. 10 in Osteology and relationships of Olorotitan arharensis, a hollow-crested hadrosaurid dinosaur from the latest Cretaceous of Far Eastern Russia
Fig. 10. Left dentary of hadrosaurid dinosaur Olorotitan arharensis Godefroit, Bolotsky, and Alifanov, 2003 (AEHM 2/845, holotype), from the Upper Cretaceous of Kundur (Russia), in medial (A), lateral (B), and dorsal (C) views. Photographs (A1, B1), explanatory drawings (A2, B2, C).
Fig. 5 in Cretaceous braconid wasps from the Magadan Province of Russia
Fig. 5. Braconid wasp Cretorhyssalus brevis gen. et sp. nov., holotype of male (?), PIN, 3901/81, Habitus in lateral view, Obeshchayushchiy fossil site (Magadan Province, Russia), Earliest Upper Cretaceous. Photograph (A) and drawing (B). Scale bars 1 mm.
Fig. 3 in Cretaceous braconid wasps from the Magadan Province of Russia
Fig. 3. Photographs of braconid wasp Magadanobracon zherikhini gen. et sp. nov., holotype of male (?), Obeshchayushchiy fossil site (Magadan Province, Russia), Earliest Upper Cretaceous. A. PIN, 3901/79, counterpart; A1, habitus; A2, head, mesosoma, and basal part of metasoma. B. PIN, 3901/80, part; B1, habitus (part); B2, fore wing (part); B3, body (part). Scale bars 1 mm.
Fig. 1 in Cretaceous braconid wasps from the Magadan Province of Russia
Fig. 1. Braconid wasp Magadanobracon rasnitsyni gen. et sp. nov., holotype of female, PIN, 3901/77 (part and counterpart), Obeshchayushchiy fossil site (Magadan Province, Russia), Earliest Upper Cretaceous. A. Habitus (part). B. Habitus (counterpart). C. Wings. Photographs (A1, B1) and drawings (A2, B2, C). Scale bars 1 mm.
Fig. 2 in Cretaceous braconid wasps from the Magadan Province of Russia
Fig. 2. Photographs of braconid wasp Magadanobracon rasnitsyni gen. et sp. nov., holotype of female, PIN, 3901/77 (part and counterpart), Obeshchayushchiy fossil site (Magadan Province, Russia), Earliest Upper Cretaceous. A. Antenna. B. Head and mesosoma. C. Fore and hind wings. D. Propodeum and metasoma. E. Hind leg. Scale bars 1 mm.
Fig. 3 in An enigmatic early?palaeocope ostracode from the Arenig of NW Russia
Fig. 3. Lavachilina evae sp. nov. A. TUG 1/1099, Lava River, Russia, Volkhov Stage. Right valve. In lateral (A1), × 17; oblique ventral (A2), × 17; ventral (A3), × 17; posterior (A4) views, × 23; detail of posterior view (A5), × 85; and detail of posterior view (A6), × 54. B. TUG 5/1099, Lava River, Russia, Volkhov Stage. Right valve. In lateral (B1), × 17; oblique ventral (B2), × 17; and ventral (B3) views, × 17. C. TUG 3/1099, Lava River, Russia, Volkhov Stage. Left late preadult valve. In oblique lateral (C1), × 19; lateral (C2), × 19; and ventral (C3) views, × 19. D. TUG 4/1099, Putilovo, Russia, Volkhov Stage. Deformed carapace. In anterior (D1), × 17; and antero−ventral, detail (D2) views, × 89. E. TUG 2/1099, Putilovo, Russia, Volkhov Stage. Left valve. Interior view (E1), × 19; cross−section of the valve (E2), × 61; adductorial muscle scar area (E3), × 42.
FIGURE 1. Eopelobates aff. E in Two pelobatid frogs from the late Miocene of Caucasus (Russia)
FIGURE 1. Eopelobates aff. E. bayeri from Volchaya Balka locality, Russia (late Miocene, early Turolian). 1-2, frontoparietal (GIN 1143-200) in dorsal (1) and ventral (2) views; 3-4, frontoparietal (GIN 1143-201) in dorsal (3) and ventral (4) views; 5-6, right maxilla (GIN 1143-202) in labial (5) and lingual (6) views; 7-8, right maxilla (GIN 1143-203) in labial (7) and lingual (8) views; and 9-10,?left maxilla (GIN 1143-204) in labial (9) and lingual (10) views. Scales equal 1 mm.
FIGURE 4 in Two pelobatid frogs from the late Miocene of Caucasus (Russia)
FIGURE 4. Occurrences of Eopelobates from the Paleogene (circles) and Neogene (squares) of Europe. Co-occurrences with Pelobates are indicated by open symbols. 1, Prémontré in France (Eopelobates aff. E. hinschei), MP 10, early Eocene (Duffaud, 2000); 2, Messel in Germany (E. wagneri), MP 11, middle Eocene (Wuttke, 2012); 3, Geiseltal in Germany (E. hinschei), MP 13, middle Eocene (Estes, 1970); 4, Hordle Cliff in UK (Eopelobates cf. E. hinschei), late Eocene (Milner et al., 1982); 5, Headon Hill in UK (cf. Eopelobates), late Eocene (Rage and Ford, 1980); 6, Quercy in France (cf. Eopelobates), late Eocene (Crochet et al., 1981); 7, Hoogbutsel, Hoeleden, and Boutersem TGV in Belgium (E. bayeri), MP 21, early Oligocene (Smith, 2003); 8, Sieblos in Germany (Eopelobates sp.), early Oligocene (Gaudant, 1985); 9, Rott in Germany (E. anthracinus), MP 30, late Oligocene (Parker, 1929); 10, Bechlejovice in Czech Republic (E. bayeri), late Oligocene (Špinar, 1952, 1972); 11, Oberleichtersbach in Germany (Eopelobates sp.), MP 30, late Oligocene (Böhme, 2008); 12, Dolnice in Czech Republic (Eopelobates sp.), MN 4, early Miocene (Hodrová, 1987b); 13, Sandelzhausen in Germany (Eopelobates sp.), MN 5, early Miocene (Böhme, 2010); 14, Devínska Nová Ves in Slovakia (E. bayeri), middle Miocene (Hodrová, 1988); 15, Suchomasty in Czech Republic (Eopelobates sp.), MN 10, late Miocene (Hodrová, 1987a); 16, Volchaya Balka in Russia (Eopelobates aff. E. bayeri), MN 11, late Miocene (this paper); 17, Osztramos 1 in Hungary (Eopelobates sp.), MN 14, Pliocene (Venczel, 2001); 18,?Ivanovce in Slovakia (?Eopelobates cf. bayeri), MN 15, Pliocene (Hodrová, 1981); 19,?Węże 1 in Poland (Eopelobates sp.), MN 15, Pliocene (Młynarski, 1961, 1962; Sanchíz and Mlynarski, 1979); and 20,?Rębielice Królewskie 1 in Poland (Eopelobates sp.), MN16, Pliocene (Sanchíz and Mlynarski, 1979). Data on taxonomic composition of Eopelobates are based mainly on Roček et al. (2014). The unconfirmed occurrences are denoted by a question-mark.
FIGURE 2. Eopelobates aff. E in Two pelobatid frogs from the late Miocene of Caucasus (Russia)
FIGURE 2. Eopelobates aff. E. bayeri from Volchaya Balka locality, Russia (late Miocene, early Turolian). 1-3, presacral vertebra (GIN 1143-212) in dorsal (1), ventral (2), and lateral (3) views; 4-5, presacral vertebra (GIN 1143-213) in dorsal (4) and lateral (5) views; 6-8, sacral vertebra (GIN 1143-221) in dorsal (6), ventral (7), and anterior (8) views; and 9-11, left ilium (GIN 1143-222) in lateral (9) and medial (10) views, and outline of the junctura ilioischiadica in caudal view (11). Scales equal 1 mm.
FIGURE 3 in Two pelobatid frogs from the late Miocene of Caucasus (Russia)
FIGURE 3. Pelobates sp. (1-11) and Pelobatidae indet. (12-15) from Volchaya Balka and Gaverdovsky localities, Russia (late Miocene, early Turolian). 1-2, frontoparietal (GIN 1143-223) in dorsal (1) and ventral (2) views; 3-4, left maxilla (GIN 1143-225) in labial (3) and lingual (4) views; 5-6, right maxilla (GIN 1143-226) in labial (5) and lingual (6) views; 7-9, presacral vertebra (GIN 1143-231) in dorsal (7), ventral (8), and lateral (9) views; 10-11, sacral vertebra (GIN 1144-201) in dorsal (10) and ventral (11) views; 12-13, premaxilla (GIN 1144-202) in lingual (12) and labial (13) views; and 14-15, left scapula (GIN 1143-233) in dorsal (14) and ventral (15) views. Scales equal 1 mm.
Figure 5 in The formation of the consortia relations of Molipteryx fuliginosa (Uhler, 1860) (Hemiptera, Coreidae) with Ambrosia artemisiifolia in the Primorskii Krai of Russia
Figure 5. Damage to Ambrosia artemisiifolia: a - drying of parts of shoots with leaf plates; b - disruption of the development of inflorescences.
Figure 4 in The formation of the consortia relations of Molipteryx fuliginosa (Uhler, 1860) (Hemiptera, Coreidae) with Ambrosia artemisiifolia in the Primorskii Krai of Russia
Figure 4. Eggs laid by the bug-riddling on the leaf plate Cirsium pendulum (a) and the stem and leaf plate of Ambrosia artemisiifolia (b).
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.