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.
153
datasets available to search
ShareScore release 0.7.1
Dataset results
153 results for “Eastern Europe”
Figure 4 in Genetic lineages of Parisotoma notabilis sensu lato (Collembola) in Eastern Europe and the Caucasus
Figure 4. Sites of lineage findings in the Caucasus region and in southern Eastern Europe (L0, L1, L2, L3, L4-Hebert, L-Hyrcan, L-Crimea, L-Cheget, L-Georgia, L-Khosta).
Figure 1 in Genetic lineages of Parisotoma notabilis sensu lato (Collembola) in Eastern Europe and the Caucasus
Figure 1. Maximum Likelihood genetic tree of 10 lineages of P. notabilis based on the COI gene fragment.
Text-fig. 2. Main geological structures of the eastern slope of the Sikhote-Alin' ridge and main plant-bearing localities of the Cenozoic floras. I – Mesozoic folded basement; II – East Sikhote-Alin' Volcanic Belt (Late Cretaceous–Early Palaeocene); III – Near-Shore Basaltic Volcanic Belt (Eocene–Early Miocene); IV – Udyl Basin (Cenozoic); V – Late Neogene to Quaternary plateaubasalts; Va – Sovgavan plateau; Vb – Samarga plateau; Vc – Bikin plateau. 1 – Malo-Mikhaylovka; 2 – Siziman; 3 – Sjurkum; 4 – Botchi; 5 – Dembi; 6 – Bui; 7 – Sonje; 8 – Takhobe; 9 – Amgu; 10 – Velikaya Kema; 11 – Zerkal'naya (former Tadushi). in Mid-Latitude Palaeogene Floras Of Eurasia Bound To Volcanic Settings And Palaeoclimatic Events - Experience Obtained From The Far East Of Russia (Sikhote-Alin') And Central Europe (Bohemian Massif)
Text-fig. 2. Main geological structures of the eastern slope of the Sikhote-Alin' ridge and main plant-bearing localities of the Cenozoic floras. I – Mesozoic folded basement; II – East Sikhote-Alin' Volcanic Belt (Late Cretaceous–Early Palaeocene); III – Near-Shore Basaltic Volcanic Belt (Eocene–Early Miocene); IV – Udyl Basin (Cenozoic); V – Late Neogene to Quaternary plateaubasalts; Va – Sovgavan plateau; Vb – Samarga plateau; Vc – Bikin plateau. 1 – Malo-Mikhaylovka; 2 – Siziman; 3 – Sjurkum; 4 – Botchi; 5 – Dembi; 6 – Bui; 7 – Sonje; 8 – Takhobe; 9 – Amgu; 10 – Velikaya Kema; 11 – Zerkal'naya (former Tadushi).
Text-fig. 3. Distribution of main types of volcanoes in the NearShore Volcanic Belt of Eastern Sikhote-Alin' (Eocene–Neogene). 1 – Central volcanoes (partly preserved); 2 – Central volcanoes (destructed); 3 – Shield and gentle sloping volcanoes with a dolerite or trachy-basaltic neck on the top; 4 – Lava and scoria cones; 5 – Pyroclastic, tuffaceous coarse- and fine-grained terrigenous sedimentary rocks, partly with plant-bearing levels; 6 – Eruption centers of plateau-basalts and the direction of lava flows; 7 – Main Late Cenozoic basaltic plateaus; 8 – Fumarol fields; 9 – Hot springs. in Mid-Latitude Palaeogene Floras Of Eurasia Bound To Volcanic Settings And Palaeoclimatic Events - Experience Obtained From The Far East Of Russia (Sikhote-Alin') And Central Europe (Bohemian Massif)
Text-fig. 3. Distribution of main types of volcanoes in the NearShore Volcanic Belt of Eastern Sikhote-Alin' (Eocene–Neogene). 1 – Central volcanoes (partly preserved); 2 – Central volcanoes (destructed); 3 – Shield and gentle sloping volcanoes with a dolerite or trachy-basaltic neck on the top; 4 – Lava and scoria cones; 5 – Pyroclastic, tuffaceous coarse- and fine-grained terrigenous sedimentary rocks, partly with plant-bearing levels; 6 – Eruption centers of plateau-basalts and the direction of lava flows; 7 – Main Late Cenozoic basaltic plateaus; 8 – Fumarol fields; 9 – Hot springs.
Fig. 6 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 6. Ground squirrel Spermophilus praecox sp. nov. from the late Pliocene and Early Pleistocene of southern Ukraine: Kryzhanovka 2 (A, J), Kotlovina 2 (E, F, K, L, Q, R), Kotlovina 3 (G, M, S), Yuzhny (B, N, T, U), Morskoy (C, D, H, I, V, W); upper cheek teeth (A–D, P3; E–I, P4; J–P, M1–M2; Q–W, M3), in occlusal views. A. ZIN 105160/1. B. GIN 1166/1. C. NMNHU-P MoT-2. D. NMNHU-P MoT-4. E. NMNHU-P 41-5588. F. NMNHU-P 41-5589. G. NMNHU-P 41-5611. H. NMNHU-P MoT-6. I. NMNHU-P MoT-10. J. ZIN 105160/5. K. NMNHU-P 41-5598 (holotype). L. NMNHU-P 41-5599. M. NMNHU-P 41-5613. N. GIN 1166/4. O. NMNHU-P MoT-14. P. NMNHU-P MoT-16. Q. NMNHU-P 41-5601. R. NMNHU-P 41-5602. S. NMNHU-P 41-5616. T. GIN 1166/11. U. GIN 1166/12. V. NMNHU-P MoT-31. W. NMNHU-P MoT-32. C, J, K, O, Q, S (inverted).
Fig. 8 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 8. Temporally-calibrated dental variation in P3, P4, M1–M2, M3, p4, and m3 of Spermophilus praecox sp. nov. and Spermophilus nogaici (Topachevsky, 1957). Abbreviations: anl, anteroloph; ants, antesinus; ast, anterostyle; antd, anteroconulid; anv, anterior valley; encd, entoconulid; enl, endoloph; hyd, hypoconid; hyp, hypocone; lanld, labial anterolophid; LH, Late Pleistocene–Holocene; lianld, lingual anterolophid; limtl, lingual metaloph; limtld, lingual metalophid; mes, mesostyle; metl, metaconule; pofd, postflexid; pro, protocone.
Fig. 9 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 9. Stratigraphic record of P3 (A), p4 (B), M1–M2 (C), and m1–m2 (D) sizes of Spermophilus praecox sp. nov. (circles) and Spermophilus nogaici Topachevsky, 1957) (triangles). Abbreviations: L, length; W, width; tal.W, talonid width; tri.W, trigonid width.
Fig. 4 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 4. Ground squirrel Spermophilus nogaici (Topachevsky, 1957) from the Early and Middle Pleistocene of southern Ukraine and southwestern Russia: Zhevakhova Gora 1 (A, C, N), Tarkhankut (D–F, O, T), Nogaisk (G–J, P, U–W, Z), Moiseevo 1 (Q), Cherevichnoe 1 (B, X), Tihonovka 1 (K, L), Bolshevik 2,I (M), lower cheek teeth (A, B, dp4; C–M, p4; N–S, m1–m2; T–Y, m3; Z, p4–m3), in occlusal (A–Z1), labial (Z2), and lingual (Z3) views. A. NMNHU-P ZG1-20. B. NMNHU-P Che1-41. C. NMNHU-P ZG1-24. D. NMNHU-P 50-26/65. E. NMNHU-P 50-26/110. F. NMNHU-P 50-26/122. G. NMNHU-P 27-106. H. NMNHU-P 27-540. I. NMNHU-P 27-541. J. NMNHU-P 27-543. K. NMNHU-P 29-4066. L. NMNHU-P 29-4075. M. NMNHU-P Bol2/1- 64. N. NMNHU-P ZG1-25. O. NMNHU-P 50-25/131. P. NMNHU-P 27-575. Q. ZIN 105151/33. R. NMNHU-P 29-4079. S. NMNHU-P Bol2/1-73. T. NMNHU-P 50-26/56. U. NMNHU-P 27-161. V. NMNHU-P 27-163. W. NMNHU-P 27-172. X. NMNHU-P Che1-68. Y. NMNHU-P 29-4099. Z. NMNHU-P 27-224. B, D, H, L, T, U, Y (inverted).
Fig. 2 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 2. Upper (A) and lower (B) sciurid cheek teeth illustrating the terminology employed here (after Marivaux et al. 2004; Comte et al. 2012; VianeyLiaud et al. 2013; and Maridet et al. 2017; with modifications). Abbreviations: aam, anterior arm of metacone (premetacrista sensu Comte et al. 2012; Vianey-Liaud et al. 2013); aap; anterior arm of protocone; aapa, anterior arm of paracone; alas, anterolabial sinus; anl, anteroloph; ansd, anterosinusid; ant, anterocone; ants, antesinus; ast, anterostyle; antd, anteroconulid; anv, anterior valley; cev, central valley; ecl, ectoloph; ecld, ectolophid; encd, entoconulid; end, entoconid; endr, entoconid ridge; enl, endoloph; enld, entolophid; esd, ectostylid; hyd, hypoconid; hyld, hypoconulid; hyld II, hypoconulid II (second hypoconulid); hyp, hypocone (hypostyle sensu Popova 2016); hyst, hypostyle (hypostyle 2 sensu Popova 2016); lamtl, labial metaloph; lamtld, labial metalophid; lanld, labial anterolophid; laprl, labial protoloph; lianld, lingual anterolophid; liansd, lingual anterosinusid; limtl, lingual metaloph; limtld, lingual metalophid; liprl, lingual protoloph; mecd, mesoconid; med, metaconid; mes, mesostyle; mesd, mesostylid; mesl, metastyle; met, metacone; metd, metastylid; metdtc, metastylid crest; metl, metaconule; metl II, metaconule II (second metaconule); mtld, metalophid; pap, posterior arm of paracone (postparacrista sensu Comte et al. 2012; Vianey-Liaud et al. 2013); par, paracone; parl, paraconule; pasl, parastyle; pasl II, parastyle II (second parastyle); plas, posterolabial sinus; poc, posterocone; pofd, postflexid; pol, posteroloph; pold, posterolophid; pov, posterior valley; prd, protoconid; pro, protocone; prst, protostyle; sd, sinusid; sin, sinus; talb, talonid basin; trdb, trigonid basin.
Fig. 5 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 5. Ground squirrel Spermophilus praecox sp. nov. from the Early Pleistocene of southern Ukraine: Kotlovina 3 (A) and Morskoy (B, C); mandibles in lateral (A1–C1), and medial (A2–C2) views. A. ZIN 105163/1. B. ZIN NMNHU-P MoT-63 (inverted). C. NMNHU-P MoT-64.
Fig. 3 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 3. Ground squirrel Spermophilus nogaici (Topachevsky, 1957) from the Early and Middle Pleistocene of southern Ukraine and southwestern Russia: Tarkhankut (A, B, G, H, I, O, U), Zhevakhova Gora 1 (F, N, T), Nogaisk (C, J, K, P, V, W, X), Moiseevo 1 (Q), Tihonovka 1 (D, L, R, S, Y, Z), Bolshevik 2,I (M); upper cheek teeth (A–E, P3; F, G, DP4; H–M, P4; N–S, M1–M2; T–Y, M3; Z, P3–M3), in occlusal (A–Z1), labial (Z2), and lingual (Z3) views. A. NMNHU-P 50-29/10. B. NMNHU-P 50-29/11. C. NMNHU-P 27-230. D. NMNHU-P 29-212. E. NMNHU-P Bol2/1-4. F. NMNHU-P ZG1-1. G. NMNHU-P 50-29/69. H. NMNHU-P 50-29/25. I. NMNHU-P 50-29/27. J. NMNHU-P 27-123. K. NMNHU-P 27-239. L. NMNHU-P 29- 216. M. NMNHU-P Bol2/1-24. N. NMNHU-P ZG1-13. O. NMNHU-P 50-27/5. P. NMNHU-P 27-110. Q. ZIN 105151/12. R. NMNHU-P 29-4037. S. NMNHU-P 29-4043. T. NMNHU-P ZG1-17. U. NMNHU-P 50-28/42. V. NMNHU-P 27-535. W. NMNHU-P 27-532. X. NMNHU-P 27-121. Y. NMNHU-P 29-4059. Z. NMNHU-P 29-4036. A–C, D, H–J, P, Q, T, X (inverted).
Fig. 7 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 7. Ground squirrel Spermophilus praecox sp. nov. from the late Pliocene and Early Pleistocene of southern Ukraine: Kotlovina 2 (A, B, H–J), Kotlovina 3 (C, J–L, U, V, Z), Kryzhanovka 2 (T), Yuzhny (M–O), Morskoy (D–G, P–S, W–Y); lower cheek teeth (A–G, p4; H–S, m1–m2; T–Y, m3; Z, p3–m3), in occlusal (A–Z1), labial (Z2), and lingual (Z3) views. A. NMNHU-P 41-5603. B. NMNHU-P 41-5604. C. NMNHU-P 41-5617. D. NMNHU-P MoT-34. E. NMNHU-P MoT-36. F. NMNHU-P MoT-39. G. NMNHU-P MoT-43. H. NMNHU-P 41-5606. I. NMNHU-P 41-5610. J. NMNHU-P 41- 5621. K. NMNHU-P 41-5622. L. NMNHU-P 41-5624. M. GIN 1166/13. N. GIN 1166/15. O. GIN 1166/16. P. NMNHU-P MoT-48. Q. NMNHU-P MoT-47. R. NMNHU-P MoT-50. S. NMNHU-P MoT-57. T. ZIN 105160/7. U. NMNHU-P 41-5627. V. NMNHU-P 41-5626. W. NMNHU-P MoT-58. X. NMNHU-P MoT-60. Y. NMNHU-P MoT-61. Z. ZIN 105163/1. B, G, Q, R, X, Y (inverted).
Fig. 1 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 1. Geographic location of Spermophilus-bearing fossil localities (stars) discussed in the text.
Linked collectors and determiners for: Quercus cerris populations from Central-Eastern Europe and Middle East (IBBR-QUERCUS-CERRIS).
Natural history specimen data linked to collectors and determiners held within, "Quercus cerris populations from Central-Eastern Europe and Middle East (IBBR-QUERCUS-CERRIS)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/3a80944e-06ce-4226-ac9f-052ff0dcbd97">https://bionomia.net/dataset/3a80944e-06ce-4226-ac9f-052ff0dcbd97</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/3a80944e-06ce-4226-ac9f-052ff0dcbd97">https://gbif.org/dataset/3a80944e-06ce-4226-ac9f-052ff0dcbd97</a>. Formatted as a Frictionless Data package.
Unravelling the habitat preferences of two closely related bumble bee species in Eastern Europe
Open the record for dataset details and reuse information.
A genomic data set of single‐nucleotide polymorphisms (SNPs) generated by ddRAD tag sequencing in Q. petraea (Matt.) Liebl. populations from Central-Eastern Europe and Balkan Peninsula
<p>This genomic dataset provides highly variable single-nucleotide polymorphism (SNP) markers from georeferenced natural <em>Quercus petraea</em> (Matt.) Liebl. populations collected in Bulgaria, Hungary, Romania, Serbia, Bosnia and Herzegovina, Kosovo and Albania. These SNP loci can be used to assess genetic diversity, differentiation, population structure, and can also be used to detect signatures of selection and local adaptation.</p>
Raster and original working data for the paper Holocene matters: landscape history accounts for current species richness of vascular plants in forests and grasslands of eastern Central Europe
<p>Aim: Current species-richness patterns are sometimes interpreted as a legacy of landscape history, but historical processes shaping the distribution of species during the Holocene are frequently omitted in biodiversity models. Here, we test their importance in modelling current species richness of vascular plants in forest and grassland vegetation.<br> Location: Western Carpathians and adjacent regions.<br> Taxon: Vascular plants.<br> Methods: Numbers of all species and of habitat specialists were extracted from plot records of forest and grassland vegetation. For each plot, environmental and historical data were derived from thematic maps. Historical data related to the persistence of (i) temperate taxa during the Late Glacial and Early Holocene, (ii) open-landscape taxa during the Middle Holocene, and (iii) taiga species during the Late Holocene were based on 112 fossil pollen profiles. Boosted regression trees were used to model spatial patterns in species richness.<br> Results: Historical variables always appeared among the best predictors of current species richness. In light forests, species richness highly mirrored both the Late Glacial (12.5% contribution) and Middle-Holocene (8.6%) landscape history. The latter factor became an important predictor also for species richness of steppe grasslands (8.3%) along with temperature seasonality (11.9%). Species richness of dark coniferous forests was best predicted by the Late-Holocene occurrence of taiga forests (14.8%), which had an even stronger effect on the richness of habitat specialists (20.5%). <br> Main conclusions: Landscape changes since the Last Glacial Maximum are important predictors of current plant species richness. The historical effects were found to be habitat-specific and, because they may interact with recent environmental conditions and anthropogenic pressures, they often show a non-linear relationship with species richness. We provide one possible direction of incorporating past landscape changes into the models of species richness.</p>
Code and data to "The shifting of buffer crop repertoires in pre-industrial north-eastern Europe "
<p>This code and data can be used to replicate the plots and figures of the paper and to trace the correlation and tests of climate variability and crop development in the study area.</p> <p> </p>
Figs 11–12 in New Records Of The Subfamilies Cylloceriinae And Microleptinae (Hymenoptera, Ichneumonidae) From Eastern Europe
Figs 11–12. Microleptes splendidulus: 11 — habitus (lateral view); 12 — face (frontal view).
Fig. 2 in Testate Amoebae in Karst Caves of the Dinaric Arc (South-Eastern Europe) with a Description of Centropyxis bipilata sp. nov.
Fig. 2. Total number of detected testate amoebae per cave
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.