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153 results for “eastern Europe”
Figure 16 from: Kasparek M (2018) Taxonomic revision proves Trachusa pubescens (Morawitz, 1872) sensu lato to be a complex of allopatric and sympatric species in South-Eastern Europe and Western Asia (Hymenoptera, Apoidea, Anthidiini). ZooKeys 764: 111-144. https://doi.org/10.3897/zookeys.764.24581
Figure 16 Discriminant Analysis (DA) of the 26 morphometric characters of males of Trachusa balcanica sp. n., T. hakkariensis sp. n., and T. maxima. Members of these OUs are characterised by an emarginate clypeus and subacute lateral projections of T6. Trachusa maxima is subdivided into the Armenian OU (including one specimen from central Iran) and the Anatolian OU.
Figure 7 from: Kasparek M (2018) Taxonomic revision proves Trachusa pubescens (Morawitz, 1872) sensu lato to be a complex of allopatric and sympatric species in South-Eastern Europe and Western Asia (Hymenoptera, Apoidea, Anthidiini). ZooKeys 764: 111-144. https://doi.org/10.3897/zookeys.764.24581
Figure 7 Dorsal view of the apical margin of T6 in the five species of the Trachusa pubescens complex. The dotted line is added to show the relative length of the median projection in relation to the lateral projections. Arrows indicate distinguishing features.
Figure 8 from: Kasparek M (2018) Taxonomic revision proves Trachusa pubescens (Morawitz, 1872) sensu lato to be a complex of allopatric and sympatric species in South-Eastern Europe and Western Asia (Hymenoptera, Apoidea, Anthidiini). ZooKeys 764: 111-144. https://doi.org/10.3897/zookeys.764.24581
Figure 8 Dorsal view of the apex of the median projection of T7 in the five species of the Trachusa pubescens complex.
Figure 3 from: Kasparek M (2018) Taxonomic revision proves Trachusa pubescens (Morawitz, 1872) sensu lato to be a complex of allopatric and sympatric species in South-Eastern Europe and Western Asia (Hymenoptera, Apoidea, Anthidiini). ZooKeys 764: 111-144. https://doi.org/10.3897/zookeys.764.24581
Figure 3 Principal Component Analysis (PCA) of 26 morphometric characters (males) of those OUs of the Trachusa pubescens complex whose members are characterised by an emarginate clypeus and subacute lateral projections on T6.
Figure 6 from: Kasparek M (2018) Taxonomic revision proves Trachusa pubescens (Morawitz, 1872) sensu lato to be a complex of allopatric and sympatric species in South-Eastern Europe and Western Asia (Hymenoptera, Apoidea, Anthidiini). ZooKeys 764: 111-144. https://doi.org/10.3897/zookeys.764.24581
Figure 6 Comparison of the clypeus index (clypeus width / clypeus length) in males of the five species of the Trachusa pubescens complex. Abbreviations: bal = T. balcanica sp. n.; hak = T. hakkariensis sp. n.; max = T. maxima; pub = T. pubescens; ver = T. verhoeffi.
Supplementary material 2 from: Czúcz B, Kalóczkai Á, Arany I, Kelemen K, Papp J, Havadtői K, Campbell K, Kelemen M, Vári Á (2018) How to design a transdisciplinary regional ecosystem service assessment: a case study from Romania, Eastern Europe. One Ecosystem 3: e26363. https://doi.org/10.3897/oneeco.3.e26363
Key elements of the participatory approach in the Niraj-MAES project
Supplementary material 1 from: Czúcz B, Kalóczkai Á, Arany I, Kelemen K, Papp J, Havadtői K, Campbell K, Kelemen M, Vári Á (2018) How to design a transdisciplinary regional ecosystem service assessment: a case study from Romania, Eastern Europe. One Ecosystem 3: e26363. https://doi.org/10.3897/oneeco.3.e26363
Definition of key terms, as used in the study
Supplementary material 3 from: Czúcz B, Kalóczkai Á, Arany I, Kelemen K, Papp J, Havadtői K, Campbell K, Kelemen M, Vári Á (2018) How to design a transdisciplinary regional ecosystem service assessment: a case study from Romania, Eastern Europe. One Ecosystem 3: e26363. https://doi.org/10.3897/oneeco.3.e26363
Supplementary tables with additional justification for individual ES indicators
Figure 2 in Genetic lineages of Parisotoma notabilis sensu lato (Collembola) in Eastern Europe and the Caucasus
Figure 2. Maximum Likelihood genetic tree of P. notabilis s. l. based on the D3−D5 region of 28S gene.
Figure 1 in Discovering underground bat hibernacula in lowland eastern Europe
Figure 1. Location of the examined underground sites. Numbers correspond to those in the list of Annex 1.
FIGURE 5 in Rubus gayeri and Rubus slavonicus, two new species of Rubus ser. Micantes (Rosaceae) from Central and South-Eastern Europe
FIGURE 5. Distribution maps: (a) Rubus gayeri; (b) Rubus slavonicus
Data from: Taxon-level assessment of the data collection quality in Atlas Florae Europaeae: insights from the case of Rosa (Rosaceae) in Eastern Europe
<p>By the method of data re-collection and re-assessment, we tested the completeness of distribution areas of the species and species aggregates of <i>Rosa</i> in Eastern Europe as mapped in volume 13 of <i>Atlas Florae Europaeae</i>, and discussed insights into the issues connected with the data. We have found many new occurrences which are additions to the published maps: 1068 records of species and 570 records of species aggregates. The new occurrences are listed with references to the sources, and the updated AFE maps are provided. The greatest increase by new native occurrences was revealed for the species that are widespread or taxonomically complicated, and by new alien occurrences for the species that expand their secondary distribution areas. The mapping work published in 2004 is considered good, with minor omissions caused by possible oversights and incomplete sampling. The majority of new additions originated in the period after the original data collection. Nearly the same amount of new data originated from larger and smaller herbarium collections, underlining the value of small collections for chorological studies. We found that only ca. 20% of new records based on herbarium specimens have been published, thus highlighting the need of data papers for publication of distributional data. The greatest increase by new records based on herbarium specimens was found for insufficiently studied territories (Belarus, central, northern and eastern parts of Russia), whereas the same level of increase for the territories with reasonably good coverage (Latvia) was achieved by observations. We conclude that the overall sparsity of published records in Eastern Europe was caused by a lower level of data collection rather than by the poor data availability, and that floristic surveys based on herbarium specimens cannot compete in speed and density of records with observation-based surveys, which may become the main source of distributional information in the future.</p>
FIGURES 30–31 in Trifurcula (Glaucolepis) lituanica sp. nov., an unexpected new stem-miner on Salvia pratensis occurring in eastern Europe (Lepidoptera: Nepticulidae)
FIGURES 30–31. Trifurcula (Glaucolepis) lituanica, habitat in Lithuania, Ringovė, 17.viii.2005.
FIGURE 29 in Trifurcula (Glaucolepis) lituanica sp. nov., an unexpected new stem-miner on Salvia pratensis occurring in eastern Europe (Lepidoptera: Nepticulidae)
FIGURE 29. Trifurcula (Glaucolepis) lituanica, life history.
Figure 1 from: Iorgu IS, Iorgu EI, Puskás G, Ivković S, Borisov S, Gavril VD, Chobanov DP (2016) Geographic distribution of Gryllotalpa stepposa in south-eastern Europe, with first records for Romania, Hungary and Serbia (Insecta, Orthoptera, Gryllotalpidae). ZooKeys 605: 73-82. https://doi.org/10.3897/zookeys.605.8804
Figure 1 - Inner part of hind tibia: A Gryllotalpa unispina B Gryllotalpa stepposa C Gryllotalpa gryllotalpa. Dorsal view of male tegminae: D Gryllotalpa unispina E Gryllotalpa stepposa F Gryllotalpa gryllotalpa. Distal part of the median vein (♂): G Gryllotalpa stepposa H Gryllotalpa gryllotalpa. Epiphallus: I Gryllotalpa unispina J Gryllotalpa stepposa K Gryllotalpa gryllotalpa. Locations: Gryllotalpa unispina – Letea; Gryllotalpa stepposa – Șura Mare; Gryllotalpa gryllotalpa – Pașcani (Romania). Scale bars 1 mm.
Figure 2 from: Iorgu IS, Iorgu EI, Puskás G, Ivković S, Borisov S, Gavril VD, Chobanov DP (2016) Geographic distribution of Gryllotalpa stepposa in south-eastern Europe, with first records for Romania, Hungary and Serbia (Insecta, Orthoptera, Gryllotalpidae). ZooKeys 605: 73-82. https://doi.org/10.3897/zookeys.605.8804
Figure 2 - Geographic distribution of Gryllotalpa species in south-eastern Europe: yellow squares – Gryllotalpa stepposa; red triangles – Gryllotalpa gryllotalpa; green hexagons – Gryllotalpa unispina; blue dots – Gryllotalpa krimbasi (although some localities are not confirmed by karyology studies, we considered them for Gryllotalpa krimbasi, based on indirect data from its distribution and nearby records).
Data from: Taxon-level assessment of the data collection quality in Atlas Florae Europaeae: insights from the case of Rosa (Rosaceae) in Eastern Europe
Open the record for dataset details and reuse information.
Data from: Genetic diversity and genomic signatures of selection among cattle breeds from Siberia, eastern and northern Europe
Domestication in the near eastern region had a major impact on the gene pool of humpless taurine cattle (Bos taurus). As a result of subsequent natural and artificial selection, hundreds of different breeds have evolved, displaying a broad range of phenotypic traits. Here, 10 Eurasian B. taurus breeds from different biogeographic and production conditions, which exhibit different demographic histories and have been under artificial selection at various intensities, were investigated using the Illumina BovineSNP50 panel to understand their genetic diversity and population structure. In addition, we scanned genomes from eight breeds for signatures of diversifying selection. Our population structure analysis indicated six distinct breed groups, the most divergent being the Yakutian cattle from Siberia. Selection signals were shared (experimental P-value < 0.01) with more than four breeds on chromosomes 6, 7, 13, 16 and 22. The strongest selection signals in the Yakutian cattle were found on chromosomes 7 and 21, where a miRNA gene and genes related to immune system processes are respectively located. In general, genomic regions indicating selection overlapped with known QTL associated with milk production (e.g. on chromosome 19), reproduction (e.g. on chromosome 24) and meat quality (e.g. on chromosome 7). The selection map created in this study shows that native cattle breeds and their genetic resources represent unique material for future breeding.
Figure 3 from: Busmachiu G, Kováč Ľ, Dana M, Weiner WM (2017) Riparian Collembola (Hexapoda) communities of northern Moldova, Eastern Europe. ZooKeys 724: 119-134. https://doi.org/10.3897/zookeys.724.12478
Figure 3 Shore of the Lake Costeşti-Stânca.
Figure 2 from: Busmachiu G, Kováč Ľ, Dana M, Weiner WM (2017) Riparian Collembola (Hexapoda) communities of northern Moldova, Eastern Europe. ZooKeys 724: 119-134. https://doi.org/10.3897/zookeys.724.12478
Figure 2 Bank of the Prut River near Branişte.
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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.
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.