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6,170 results for “european”
Distribution. SE Ukraine (E of Dnieper River), S European Russia, Greece (E Aegean Is of Kos and Rhodes), Turkey (Anatolia), Syria, Lebanon, Israel, NW Jordan, Georgia, Armenia, Azerbaijan, N Iran, and W & § Turkmenistan. in Muridae
Distribution. SE Ukraine (E of Dnieper River), S European Russia, Greece (E Aegean Is of Kos and Rhodes), Turkey (Anatolia), Syria, Lebanon, Israel, NW Jordan, Georgia, Armenia, Azerbaijan, N Iran, and W & § Turkmenistan.
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Distribution. S European Russia, S in Muridae
Distribution. S European Russia, S Kazakhstan, Uzbekistan, Turkmenistan, Kyrgyzstan, Tajikistan, NE Iran, N Afghanistan, NW & NC China (Xinjiang, Gansu, Qinghai, Inner Mongolia [= Nei Mongol], Ningxia, N Shaanxi, N Shanxi, and NW Hebei), and S Mongolia.
Dataset_ metabolic scope performance and tolerance of juvenile European sea bass Dicentrarchus labrax upon acclimation to high temperatures
<p>This dataset contains the data associated with the article 'Metabolic scope, performance and tolerance of juvenile European sea bass Dicentrarchus labrax upon acclimation to high temperatures' by Stavrakidis-Zachou et al. accepted for publication on Plos one in July 2022.</p>
Data for: European mushroom assemblages are phylogenetically structured by temperature
<p><span>Recent global warming affects species compositions at an unprecedented rate. To predict climate-induced changes in species assemblages, a better understanding of the link between species occurrence and climate is needed. Macrofungal fruit body assemblages are correlated with the thermal environment at the European scale. However, it is still unknown whether macrofungal communities are also phylogenetically structured by thermal environments. Thermal environments are characterized by annual temperature means but also by intra-annual temperature variability (hereafter termed temperature seasonality), which are both considered in this study. Here, we used distribution data of </span><span>2,882 </span><span>species based on fruit body records across Europe to address two main questions: (i) Are mushroom assemblages at the extremes of the mean (warm and cold) and seasonal (high intra-annual variability, i.e. continental) climate gradient phylogenetically more similar than expected (phylogenetic alpha diversity); (ii) are mushroom assemblages, that are subject to different mean and seasonal temperature conditions, composed of different lineages (phylogenetic beta diversity). Our phylogenetic alpha diversity analysis shows that mushroom assemblages are phylogenetically structured by warm and cold environments, indicating that phylogenetically related species with similar traits thrive under more extreme conditions. In contrast, assemblages are phylogenetically more dissimilar (overdispersed) in temperature seasonal environments, indicating limiting similarity. Phylogenetic beta diversity was significantly correlated with mean and seasonal temperature differences, a response mainly driven by a few genera. Our results show that macrofungal assemblages are phylogenetically structured by temperature across Europe, suggesting phylogenetically constrained specialization towards temperature extremes. Predicted anthropogenic warming is likely to affect species composition and phylogenetic diversity with additional consequences for the carbon- and nutrient cycles.</span></p>
A new species of the genus Dolichoderus Lund, 1831 (Hymenoptera, Formicidae) from a Late Eocene European amber. Supplementary file 2
<p>Supplementary file 2: Paleontological reconstruction (3D model) of <em>Dolichoderus jonasi</em> Dubovikoff et Zharkov, 2022 (male). </p>
A new species of the genus Dolichoderus Lund, 1831 (Hymenoptera, Formicidae) from a Late Eocene European amber. Supplementary file 1
<p>Supplementary file 1: Paleontological reconstruction (3D model) of Dolichoderus jonasi Dubovikoff et Zharkov, 2022 (worker)</p>
Figure 14. A, B, E, F in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 14. A, B, E, F, Eratigena inermis; C, D, G, H, Eratigena vomeroi; I, Tegenaria montiszasensis sp. nov.; J, Tegenaria annulata; K, L, Tegenaria schoenhoferi sp. nov.; M-P, Tegenaria annae sp. nov.; Q-T, Tegenaria ariadnae. Left male palp in ventral (A, C, K, M, Q) and retrolateral views (B, D, L, N, R); epigyne in ventral view (O, S), vulva in dorsal (E, G, I, J, P, T) and lateral views (F, H). Abbreviations: E, embolus; C, conductor; CD, copulatory duct; DA, dorsal appendages on CD; FD, fertilization duct; MA, median apophysis; RC, receptaculum; RTA d, dorsal branch of retrolateral tibial apophysis; RTA l, lateral branch of retrolateral tibial apophysis; TR, transversal ridge.
Figure 12. A, B in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 12. A, B, Eratigena herculea; C, D, H, N, O, Eratigena arganoi; E, K, Eratigena sicana; F, G, L, M, Eratigena hispanica; I, J, P, Q, Eratigena sardoa; R–T, Eratigena picta. Female epigyne in ventral (A, C, F, I) and vulva in dorsal view (B, D, E, G, J); male left palp in ventral (L, N, P, R) and retrolateral views (M, O, Q, S); frontal face of male E. arganoi (H); habitus of female E. sicana (K); habitus of two males of E. picta (T). Scale bars = 0.5 mm.
› Figure 22. A, B, Tegenaria capolongoi; C-K, Tegenaria parmenidis; L-S, Tegenaria circeoensis sp. nov. Left male palp in ventral (E, N), retrolateral (F, O), and dorsal views (G, P); epigyne in ventral (A, C, Q, S) and vulva in dorsal view (B, D, R); intraspecific epigynal morphological variation (S); face of male in frontal view (J); spinnerets in ventral view (K); habitus (H) of male in dorsal and sternum in ventral view (I); carapace and abdomen of male in dorsal view (L, M). Scale bars = 0.5 mm (except 1 mm for H). in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
› Figure 22. A, B, Tegenaria capolongoi; C-K, Tegenaria parmenidis; L-S, Tegenaria circeoensis sp. nov. Left male palp in ventral (E, N), retrolateral (F, O), and dorsal views (G, P); epigyne in ventral (A, C, Q, S) and vulva in dorsal view (B, D, R); intraspecific epigynal morphological variation (S); face of male in frontal view (J); spinnerets in ventral view (K); habitus (H) of male in dorsal and sternum in ventral view (I); carapace and abdomen of male in dorsal view (L, M). Scale bars = 0.5 mm (except 1 mm for H).
Figure 17. A, B in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 17. A, B, Tegenaria domestica; C, F, G, M, N, Tegenaria racovitzai; D, E, Q, R, Tegenaria hauseri; H-J, Tegenaria bozhkovi; K, L, O, P, Tegenaria campestris; S, T, Tegenaria pieperi; U, Tegenaria schmalfussi; V, Tegenaria faniapollinis; W, Tegenaria percuriosa (holotype of Tegenaria bithyniae); X-Z, Tegenaria croatica sp. nov. Left male palp in ventral (M, O, Q) and retrolateral views (N, P, R); epigyne in ventral (D, F, H, K, S, U–W, Y) and posterioventral views (T), vulva in dorsal (E, G, I, L, U, Z) and lateral views (J); face of female Teg. domestica (A) and Teg. racovitzai (C); cheliceral margins of female Teg. domestica in posterioventral view (B); habitus, dorsal view (X). Scale bars = 0.5 mm (no scale for Teg. faniapollinis, V, and Teg. schmalfussi, U).
Figure 13. A, B, I, J in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 13. A, B, I, J, Eratigena balearica; C, D, K, L, R, Eratigena inermis; E, F, M–Q, Eratigena vomeroi; G, H, Eratigena picta. Male left palp in ventral (A, C, E) and retrolateral views (B, D, F); epigyne in ventral (G, I, K, M) and vulva in dorsal view (H, J, L, N); carapace (O) and abdomen (Q) in dorsal view, sternum in ventral view (P, R). Scale bars = 0.5 mm.
Figure 20. A–I in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 20. A–I, Tegenaria silvestris, variation in males and females (F–I); J-M, Tegenaria parvula; N, S-V, Tegenaria henroti; O-R, Tegenaria eleonorae; W-Z, Tegenaria pindosiensis sp. nov. Left male palp in ventral (A, F, J, O, S) and retrolateral views (B, G, K, P, T); epigyne in ventral (C, H, L, Q, U, W) and vulva in dorsal (D, I, M, R, V, X) and lateral views (E); female habitus (N) and abdomen in dorsal view (Z); sternum in ventral view (Y). Scale bars = 0.5 mm (except 1 mm for N).
Figure 18. A–C in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 18. A–C, Tegenaria domestica; D-F, Tegenaria carensis; G, H, Tegenaria argaeica (female paratype); I-M, Tegenaria circeoensis sp. nov.; N-Q, Tegenaria parmenidis; R, S, Tegenaria sbordonii. Left male palp in ventral (A, D, I, N, R), retrolateral (E, J, O, S), and dorsal views (K); epigyne in ventral (B, G, L, P) and vulva in dorsal view (C, F, H, M, Q).
Figure 15. A, B in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 15. A, B, Tegenaria achaea; C-F, Tegenaria argaeica; G-J, Tegenaria armigera; K, L, O-Q, Tegenaria dalmatica; M, N, Tegenaria hasperi; R-U, Tegenaria annulata; and V, X, Tegenaria schoenhoferi sp. nov. Left male palp in lateral (C, H, L, U, W), and ventral views (D, G, K, T, V); epigyne in ventral (A, E, I, M, O, R) and vulva in dorsal view (B, F, J, N, P, S); comparison of vulva of small and large 'forms' of Teg. armigera (J); Prosoma in frontal view (Q), abdomen in dorsal view (X). Scale bars = 0.5 mm (epigyne and vulva of Teg. argaeica, E–F without scale; photos from syntype taken with digital camera through the oculars).
Figure 5 in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 5. Combined mtDNA data (cytochrome c oxidase subunit 1, nicotinamide adenine dinucleotide dehydrogenase subunit 1) Bayesian tree. Posterior probabilities of clades are expressed in percentages and given above branches. Clade support (> 50) from the resampling method (jack-knife, 1000 replications) based on parsimony analysis with implied weighting (K = 10) is given below the branches. Abbreviations: AT, Austria; BG, Bulgaria; CH, Switzerland; DE, Germany; FR, France; GR, Greece; IT, Italy; PT, Portugal; US, United States.
Figure 4 in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 4. Combined DNA data (cytochrome c oxidase subunit 1, nicotinamide adenine dinucleotide dehydrogenase subunit 1, and 28S) Bayesian tree. Posterior probabilities of clades are expressed in percentages and given above branches. Clade support (> 50) from the resampling method (jack-knife, 1000 replications) based on parsimony analysis with implied weighting (K = 10) is given below the branches. Abbreviations: AT, Austria; BE, Belgium; BG, Bulgaria; CH, Switzerland; DE, Germany; ES, Spain; FR, France; GR, Greece; IT, Italy; PT, Portugal; SE, Sweden; US, United States. ·
Figure 2 in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 2. Microscope and scanning electron microscopy pictures of character details. Plumose hairs (A) and claws (B) on tarsus I of Tegenaria dalmatica; C, embolus tip of Tegenaria ferruginea; D, male palp of Tegenaria dalmatica in ventroretrolateral view; E, retrolateral tibial apophysis in retrolateral view of Tegenaria ferruginea; F, epigyne in ventral view of Tegenaria domestica; G, long and dark spikes on the anal tubercle of Agelena labyrinthica; H, face and chelicerae, frontal view; I, cheliceral margins with teeth, ventral view; and J, sternum, ventral view, of female Eratigena atrica. Abbreviations: BT, basal portion of tegulum; C, conductor; CO, copulatory opening; CON, connection of tegulum and conductor; DB, dorsal branch; DC, distal portion of conductor; DP, dorsal part of terminal end of conductor; E, embolus; EP, epigynal plate; LB, lateral branch; LM, lateral margin of median region; MA, median apophysis; MC, lateral margin of conductor (here entirely folded); MP, median plate; MR, median region; PS, posterior sclerite (here bar- or band like); PT, 'pseudo teeth'; TEC, terminal end of conductor (here bifid); VB, ventral branch; VP, ventral part of terminal end of conductor. Scale bars for F–J = 0.5 mm.
Figure 3 in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 3. Most parsimonious strict consensus tree based on morphological data with equal character weights. Branch support is indicated by jack-knife values (1000 pseudoreplicates)/Bremer support at the nodes. Analysis with implied weighting (K = 10) resulted in additional supported clades (jack-knife support): Tegenaria mercanturensis + Tegenaria mirifica (69), Tegenaria montana + Tegenaria rilaensis (52), Tegenaria parvula + Tegenaria silvestris (55). Black dots indicate apomorpies, white dots indicate homoplasies. Numbers above the dots correspond to the character number, numbers below the dots to the character state.
Figure 1 in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
Figure 1. Scanning electron microscopy pictures of spinnerets of female and other structures. A–D, Tegenaria domestica; E, F, Tegenaria parietina; G, H, Tegenaria dalmatica; I, Eratigena agrestis; J, Eratigena atrica; K, Aterigena ligurica; L-N, Malthonica lusithanica; O, Allagelena gracilens. A, L, overview; B, D, F, I, K, N, PMS; E, H, J, ALS; M, distal segment of PLS; C, G, colulus; O, tarsal trichobothrium. Abbreviations: ALS, anterior lateral spinnerets; CGS, cylindrical gland spigot; COL, colulus; mAS, minor ampullate gland spigot; MAS, major ampullate gland spigot; N, nubbin; PGS, piriform gland spigots; PLS, posterior lateral spinnerets; PMS, posterior median spinnerets; T, tartipore; TS, tracheal stigma.
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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)
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.