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6,170 results for “european”
FIGURE 4 in Morphology and molecular data of the species of Suillus (Suillaceae, Boletales) associated with Pinus sibirica at the European northeast of Russia
FIGURE 4. Basidiocarps and elements of pileipellis. a, b Suillus punctipes (SYKOf 2598). c, d Suillus plorans (SYKOf 2666). e, f Suillus plorans ssp. cyanescens (SYKOf 3006). Scale bars a, c, e—2 сm; b, d, f—50 μm. Images: Marina Palamarchuk.
FIGURE 3. Basidiocarps. a in Morphology and molecular data of the species of Suillus (Suillaceae, Boletales) associated with Pinus sibirica at the European northeast of Russia
FIGURE 3. Basidiocarps. a Suillus acidus var. intermedius (SYKOf 1854). b S. acidus var. intermedius (SYKOf 2531). c S. placidus (SYKOf 2664). d S. placidus (SYKOf 2665). e S. sibiricus (SYKOf 2663), f S. sibiricus (SYKOf 2521). Scale bars 2 сm. Images: Marina Palamarchuk.
Term map of European Social Survey publications
<p>This is a term-map which can be visualized using <a href="https://www.vosviewer.com/">VOSviewer</a>.</p> <p>We extracted terms from titles and abstracts from Europen Social Survey publication and visualized them using VOSviewer. Terms are located close to each other if they co-occur frequently. The axes themselves don’t have any special meaning, only the relative distances are relevant. The size of the terms reflect the number of publications.</p> <p>We provide so-called "overlay" views for various countries and institutions, showing where their activity.</p>
Dataset for Spatial Heterogeneity of Uplift Pattern in the Western European Alps Revealed by InSAR Time Series Analysis
<p>ZIP file with InSAR raw and smoothed final velocity solution values</p>
Food and waterborne outbreaks data complementing the European Union One Health 2020 Zoonoses Report
<p>Food and waterborne outbreaks data reported under the framework of Directive 2003/99/EC and in accordance with the update of the technical specifications for harmonised reporting of FBOs through the EU reporting system in accordance with Directive 2003/99/EC. This dataset includes the number of outbreaks, as well as the number of human cases, hospitalisations and deaths, per causative agent. In addition, other information can include data on causative agents, food vehicles, and the factors in food preparation and handling that contributed to the food-borne outbreaks. Reporting countries can also provide information on the nature of the evidence supporting the suspicion of the food vehicle. This evidence can be epidemiological, microbiological, descriptive environmental, or based on product tracing investigations. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: PubliFBO2020_20211109: >></p>
Sample based prevalence data complementing the European Union One Health 2020 Zoonoses Report - Croatia
<p>This dataset contains monitoring data on zoonoses and zoonotic agents under the Directive 2003/99/EC. This Directive requires Member Sates (MSs) to collect, evaluate and report data on zoonoses and zoonotic agents. MSs can also report monitoring data and information on some other pathogenic microbiological agents in foodstuffs. Relevant EU legislation: Commission Regulation (EC) No 2073/2005,Commission Regulation (EC) No 1441/2007, Commission Regulation (EU) No 1086/2011, Commission Regulation (EU) No 209/2013, Commission Regulation(EU) No 217/2014.</p>
Animal population data complementing the European Union One Health 2020 Zoonoses Report
<p>This dataset includes animal population aggregated data under the framework of Directive 2003/99/EC. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: Animal_p20_20211109: >></p>
FIGURE 4 in Revision of the European species of the genus Hincksina Norman, 1903 (Bryozoa, Cheilostomatida, Flustridae)
FIGURE 4. Hincksina neptuni (Jullien in Jullien & Calvet, 1903) n. comb. A. Overview of lectotype with auto- and ovicellate zooecia (MOM INV-22462). B. Slightly oblique view on two autozooids (MNHN IB-2008-1999). C. Oblique view on the two fan shaped, oral spines (top), the distalmost pair of mural spines proximal to these (centre), and two pairs of more proximally positioned mural spines (bottom) (MNHN IB-2008-1999). D. Incompletely developed zooids at colony growth margin, note the relatively thin vertical zooecial margins from which the mural and oral spines will develop by epithelial folding during later ontogeny. E. Ooecium (lectotype, MOM INV-22462). F. Avicularia with mandibles still in place (lectotype, MOM INV-22462). Scale bars: A, D, 200 µm; B, F, 100 µm; C, E, 50 µm.
FIGURE 5 in Revision of the European species of the genus Hincksina Norman, 1903 (Bryozoa, Cheilostomatida, Flustridae)
FIGURE 5. Hincksina alice (Jullien in Jullien & Calvet, 1903) n. comb. A. Overview of lectotype (MOM INV-22545); note the differences in mural spine thickness between zooids. B. Auto- and ovicellate zooids (lectotype MOM INV-22545). C. Close-up of autozooid (MNHN IB-2008-1996). D. Periancestrular area with early astogenetic zooids having simple cylindrical and later bifid mural spines before fully developed spines appear, "a" = ancestrula (MNHN IB-2008-4009). E. Two ooecia, note also the unjointed oral and mural spines with their broad bases (MNHN IB-2008-1996). F. Avicularia, note the subrounded lucida in the lower side of the mandible (MNHN IB-2008-1996). Scale bars: A, D, 200 µm; B, 100 µm; C, E, F, 50 µm.
FIGURE 3 in Revision of the European species of the genus Hincksina Norman, 1903 (Bryozoa, Cheilostomatida, Flustridae)
FIGURE 3. Hincksina sceletos (Busk, 1858). A. Overview of lectotype, the autozooids having relatively thin mural spines (NHMUK 1899.7.1.1144). B. Close-up of autozooid; note the flattened, fan-shaped oral spines (lectotype, NHMUK 1899.7.1.1144). C. Two avicularia, the lower one showing the interior mandible with its muscle attachment scar and median lucida (lectotype, NHMUK 1899.7.1.1144). D. Ooecium (NHMUK 1908.3.23.1). E. Mural spines in lateral view (lectotype, NHMUK 1899.7.1.1144). F. Auto- and ovicellate zooids (NHMUK 1908.3.23.1). G. Several autozooids with thicker mural spines and the flattened oral spines viewed at a slightly oblique angle (NHMUK 1908.3.23.1). H. Periancestrular area showing the transition from thin, cylindrical, monomorphic spines in early astogenetic zooids to fully differentiated oral and mural spines in adult zooids (NHMUK 1908.3.23.1). Scale bars: A, F, H, 400 µm; B, C, 100 µm; D, E, 50 µm; G, 200 µm.
FIGURE 2. Hincksina synchysia n in Revision of the European species of the genus Hincksina Norman, 1903 (Bryozoa, Cheilostomatida, Flustridae)
FIGURE 2. Hincksina synchysia n. sp., holotype (MNHN-IB-2017-782), note that fragments of other organisms cover the surface of this unbleached specimen, some of which may be confused with oral or mural spines. A. Autozooids. B. Oblique view on auto- and ovicellate zooids to show the inclined rostra in some of the avicularia. C. Close-up of two autozooids and an avicularium, note the thin band of nodular cryptocyst in the lower left of the central zooid. D. Two zooids with ovicells produced by the distal avicularium at the far left, the three remaining ovicells are produced by the proximal gymnocyst of the distal autozooid, and one avicularium with a relatively pointed tip at lower right; note the nodular cryptocystal rim in the lower left of the central zooid. E. Close-up of an ovicell. Scale bars: A, B, D, 200 µm; C, E, 100 µm.
FIGURE 1 in Revision of the European species of the genus Hincksina Norman, 1903 (Bryozoa, Cheilostomatida, Flustridae)
FIGURE 1. Hincksina flustroides (Hincks, 1877). A. overview of lectotype (NHMUK 2016.6.9.2). B. Oblique view on autozooids (NHMUK 1963.3.24.2), note the presence of bifid as well as broad and slender mural spines, and the jointed spines bases (dark areas between mural rim and calcified spines). C. Close-up of avicularium (lectotype, NHMUK 2016.6.9.2). D. Ovicellate zooids (NHMUK 1963.3.24.2). Scale bars: A, 500 µm; B, 100 µm; C, 50 µm; D, 200 µm.
Supplementary material 1 from: Trégarot E, Failler P (2021) Adequacy of ecosystem services assessment tools and approaches to current policy needs and gaps in the European Union Overseas entities. One Ecosystem 6: e74170. https://doi.org/10.3897/oneeco.6.e74170
Selection of MAES tools and approaches to facilitate the uptake of Ecosystem Services in EU Overseas entities
Input data for Open-data based carbon emission intensity signals for electricity generation in European countries -- top down vs. bottom up approach
<p>This dataset contains all necessary input data to reproduce the results of the paper "Open-data based carbon emission intensity signals for electricity generation in European countries -- top down vs. bottom up approach".</p>
Output data for Open-data based carbon emission intensity signals for electricity generation in European countries -- top down vs. bottom up approach
<p>This dataset contains all output data (results) of the paper "Open-data based carbon emission intensity signals for electricity generation in European countries -- top down vs. bottom up approach".</p>
MAR-MPI-ESM1-2-HR HIST (1961-2014) and SSP245 European Alps (2015-2100)
<p>This deposit contains MAR simulations over the European Alps domain (7 kilometers resolution) forced by the MPI-ESM1-2-HR GCM (CMIP6 version) for the historical period (HIST, 1961 to 2014) and the SSP245 projection (SSP245, 2015 to 2100). The version of the MAR model used is v.3.10, model set-up is described in detail in Beaumet et al., 2021 (https://doi.org/10.1007/s10113-021-01830-x) Contact person : Julien Beaumet (beaumetjulien@gmail.com), Martin Menegoz (martin.menegoz@univ-grenoble-alpes.fr)<br> The realization used is r1i1p1f1.<br> Data are available at the daily frequency, with one variable per file (10 years of data per file).<br> The available variables in this deposit are :</p> <p><strong>CC:</strong> Cloud cover, [0-1]<br> <strong>MB:</strong> Total snow water equivalent, [mm.We]<br> <strong>MBrr:</strong> Daily rainfall, [mm.We] (5)<br> <strong>MBsf:</strong> Daily snowfall, [mm.We] (5)<br> <strong>QQz: </strong> Near-surface specific humidity at constant height, [g/kg] (2)</p> <p><strong>TTmax:</strong> Near-surface maximum air temperature for the first model level above the surface (constant sigma), [C]<br> <strong>TTmin:</strong> Near-surface minimum air temperature for the first model level above the surface (constant sigma),[C]</p> <p><strong>TTz: </strong>Near-surface mean air temperature at constant-height, [C]<br> <strong>UUz:</strong> Near-surface zonal component of wind speed at constant height, [m/s]<br> <strong>VVz:</strong> Near surface Meridional component of wind speed at constant height, [m/s]<br> <strong>ZN3:</strong> Total snow height, [m]</p> <p>Other variables are available upon request (see email above).<br> AL : Surface albedo, [0-1]<br> CD: Low level Cloud cover, [0-1]<br> CM: Middle level Cloud cover, [0-1]<br> CU: High level Cloud cover, [0-1]<br> SP: Surface pressure, [hPa]<br> ST: Surface temperature, [C]<br> TT: Near-surface mean air temperature for the first three model level above the surface (constant sigma), [C] (1)<br> TTp: Constant pressure-level mean air temperature, [C] (4)<br> ZZ: Surface geopotential for the first three model level above the surface (constant sigma), [m]</p> <p>LWD: Surface downward longwave radiation, [W/m2]<br> LWU: Surface upward longwave radiation, [W/m2]</p> <p>SWD: Surface downward shortwave radiation, [W/m2]<br> SWU: Surface upward shortwave radiation, [W/m2]</p> <p>SHF: Surface sensible heat flux, [W/m2] LHF: Surface latent heat flux, [W/m2]</p> <p>* Latitude(LAT),longitude(LON)and surface elevation (SH) of each grid point can be read in MARgrid_EUy.nc file</p> <p>(1) For variable TT, ZZ model constant sigma level of 0.9997479, 0.999496, 0.9989921<br> (2) For variables TTz, QQz constant height level are : 2, 10, 50 and 100m<br> (3) For variables UUz, VVz constant height level are : 10, 50 and 100m<br> (4) Variables TTp, UUp, VVp available at pressure level : 925, 850, 800, 700, 600, 500, 200 hPa<br> (5) Snow height and snow water equivalent are available for three sectors which corresponds to three different vegetation type : The three vegetation type used can be readen in the file MARgrid_EUy.nc, with the variable VEG and their respectibe fraction for each grid point is given by the variable FRV. The third vegetation type (sector=3) mostly corresponds to bare soil or low crops by default, but sometimes its fraction=0, which gives unrealistic low values of snow height. In this case, using the max. value on the axis sector often gives the best results.<br> Legend of the vegetation type for the VEG variables : 0:NO_VEGETATION 1:CROPS_LOW 2:CROPS_MEDIUM 3:CROPS_HIGH 4:GRASS_LOW 5:GRASS_MEDIUM 6:GRASS_HIGH 7:BROADLEAF_LOW 8:BROADLEAF MEDIUM 9:BROADLEAF_HIGH 10:NEEDLELEAF_LOW 11:NEEDLELEAF MEDIUM 12:NEEDLELEAF_HIGH 13:City<br> ~ </p>
Management alters drought-induced mortality patterns in European beech (Fagus sylvatica L.) forests
<ul> <li>The high tree mortality during the dry and hot years 2018-2019 in Europe affected not only even-aged and monospecific conifer stands but also semi-natural <i>Fagus sylvatica</i> L. (European beech) forests. This has triggered concerns on the future of European beech forests under climate change and raised questions as to whether forest management may increase tree mortality rates through creating more open canopies. We compared long-term mortality rates of beech between strict forest reserves and adjacent managed reference stands for three inventory periods at 11 sites in the federal state Hesse, Germany, near the centre of the European distribution of the species.</li> <li>We hypothesized that mortality would increase with climatic water deficits during the growing season, initial stand density, and decreasing dominance (canopy status) of trees. We also hypothesized that mortality would decrease with site moisture status and the intensity of tree removals. To quantify the influence of management, initial stand density and tree removals were used as predictor variables. In addition, we analyzed the influence of the climatic water balance and competitive status of trees on mortality.</li> <li>Mean annual natural mortality rates ranged between 0.5 % and 2.1 %. Even in the drought years beech mortality rates were surprisingly low. We observed no signs of striking canopy disintegration. The significantly higher mortality (1.6 % - 2.1 %) in unmanaged stands during the drought years 2018 and 2019 was largely confined to suppressed trees. There was no significant increase of mortality in managed stands during the drought years, but a shift of mortality towards larger canopy trees.</li> <li>Our study did not confirm a general influence of management in the form of tree removals on mortality rates. Yet, we showed that during drought years management changed the distribution of mortality within the tree community. To analyze the effect of management on mortality rates more comprehensively, a wider gradient in site moisture conditions including sites drier than in this study and longer post-drought periods should be employed.</li> </ul>
Data from: Late Cretaceous European theropod palaeobiodiversity, palaeobiogeography and the intra-Maastrichtian faunal turnover: new contributions from the Iberian fossil site of Laño
<p>A total of 227 theropod teeth have so far been recovered from the late Campanian Laño site (northern Iberian Peninsula). The teeth were studied for their qualitative and quantitative features. From the theropod sample found at Laño, seven morphotypes attributed to five taxa are identified: a medium to large abelisaurid (<i>Arcovenator</i> sp.) and four small coelurosaurians (Dromaeosauridae indet., Paraves indet., cf. <i>Paronychodon</i> sp. and cf. <i>Richardoestesia</i> sp.). Together with the ground bird <i>Gargantuavis</i> and a possible ornithomimosaur, the theropod fauna of Laño might be composed of two medium- to large-sized non-avian theropods, four small-bodied non-avian theropods and a large terrestrial bird. This makes the Laño site the richest and most diverse latest Cretaceous theropod site of Europe. Furthermore, the Laño site and the Late Cretaceous localities of Europe that have yielded theropod remains suggest that the medium- to large-sized theropods were abelisaurids or indeterminate theropods. The small theropods are more abundant, diverse and represented by different dromaeosaurids, <i>Paronychodon</i>, <i>Richardoestesia</i>, or related forms, troodontids and, probably, by other paravians. Among birds, enantiornithines, gargantuaviids and ornithurines are also common in the European Late Cretaceous sites. The theropod assemblage of Laño, together with the taxa of other Late Cretaceous sites, supports the idea that several theropod dispersal events took place during the Cretaceous. This resulted in a mixture of European endemic, Asiamerican and Gondwanan forms. This study also supports the hypothesis that the intra-Maastrichtian faunal turnover that occurred in the Ibero-Armorican landmass seems to have had no effect on theropods.</p>
FIGURE 10 in A taxonomic review of the Tracheliodes quinquenotatus (Jurine, 1807) species complex and some new records of rare European Tracheliodes A. Morawitz, 1866 (Hymenoptera, Crabronidae)
FIGURE 10. Lectotype of Crossocerus festivus Marquet. A—Habitus in dorsal view with labels; B—Habitus in profil; C— Face in front view. Black scale = 1mm.
FIGURE 6 in A taxonomic review of the Tracheliodes quinquenotatus (Jurine, 1807) species complex and some new records of rare European Tracheliodes A. Morawitz, 1866 (Hymenoptera, Crabronidae)
FIGURE 6. Holotype of Crabro quinquenotatus Jurine (Neotype of Crossocerus luteicollis Lepeletier & Brullé). A—Habitus in dorsal view with labels; B—Habitus in profil; C—Face in front view [© B. Landry, MHNG]. Black scale = 1mm.
ScienceDex guides
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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.