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6,170 results for “european”
Figures 14–18 in The European centipedes hitherto referred to Eurygeophilus, Mesogeophilus, and Chalandea (Chilopoda, Geophilomorpha): taxonomy, distribution, and geographical variation in segment number
Figures 14–18. Eurygeophilus pinguis (Brölemann, 1898), female, 27 mm long, M. La Marzola (Alps). (14) Head, dorsal (right antenna and setae not drawn). (15) Head, ventral (antennae not drawn). (16) Forcipular segment, ventral. (17) Sternum of leg-bearing segment V, ventral. (18) Last leg-bearing segment and terminal segments, ventral (right telopodite and setae on the relevant coxopleuron not drawn).
Figures 5–8 in The European centipedes hitherto referred to Eurygeophilus, Mesogeophilus, and Chalandea (Chilopoda, Geophilomorpha): taxonomy, distribution, and geographical variation in segment number
Figures 5–8. Eurygeophilus multistiliger (Verhoeff, 1899), female, 32 mm long, Coimbra (Iberian Peninsula), holotype, mounted on a slide. (5) Forcipular segment, ventral. (6) Calyx inside the left forcipule, ventral. (7) Sternum of leg-bearing segment XII. (8) Last leg-bearing segment and terminal segments, ventral. Images from light microscopy. Scale bars: 200 Mm (5); 100 Mm (6, 8); 50 Mm (7).
Figures 9–13 in The European centipedes hitherto referred to Eurygeophilus, Mesogeophilus, and Chalandea (Chilopoda, Geophilomorpha): taxonomy, distribution, and geographical variation in segment number
Figures 9–13. Eurygeophilus multistiliger (Verhoeff, 1899), female, 24 mm long, Campu Omo (Sardinia). (9) Head, dorsal (right antenna and setae not drawn). (10) Head, ventral (antennae not drawn). (11) Forcipular segment, ventral. (12) Sternum of leg-bearing segment V, ventral. (13) Last leg-bearing segment and terminal segments, ventral (right telopodite and setae on the relevant coxopleuron not drawn).
Figures 1–4 in The European centipedes hitherto referred to Eurygeophilus, Mesogeophilus, and Chalandea (Chilopoda, Geophilomorpha): taxonomy, distribution, and geographical variation in segment number
Figures 1–4. (1–3) Eurygeophilus pinguis (Brölemann, 1898), female, 33 mm long, M. La Marzola (near Trento, Alps). (1) Distal articles of the left antenna, ventral. (2) Left claw of the second maxillae, ventral. (3) Right part of the forcipular coxosternum, ventral. (4) Geophilus linearis C. L. Koch, 1835, male, 34 mm long, Cologna Veneta (near Verona, Italy): right part of the forcipular coxosternum, ventral. Arrows indicate the putative position of the forcipular chitin-lines. Micrographs from ESEM Philips XL30. Scale bars: 20 Mm (1, 2); 50 Mm (3, 4).
Plant community data for European ecoregions
<p>Patterns in macroecology are related to species occurrence across meaningful spatial and temporal scales. The dataset provided here reports species distribution data (presence-absence) for herbaceous plants across a number of European habitats (ecoregions). Species occurrence is accompanied by the corresponding plant's maximun stem height values. This dataset has been used to unveil patterns of herbaceous plant height clustering in mid-latitude European ecoregions.</p> <p>Presence-absence data for herbaceous plants were drawn from Atlas Florae Europaeae (Jalas & Suominen, 1964-1999). Associated to each species, a dominant habitat (ecoregion) was assigned according to the WWF Biomes of the World classification. Each herbaceous species in an ecoregion was characterized by its maximum stem height. Mean height values were obtained for different sources. In order to correlate clustering patterns with productivity measures, actual evapotranspiration (AET) data is also provided. AET maps were obtained from data estimated through remote sensing (Mu et al., 2011), which are publicly available in the MODIS project website (http://www.ntsg.umt.edu/project/modis/mod17.php).</p> <p>Plant distribution and trait data across Europe unveils a relation between plant height clustering and actual evapotranspiration. This clustering is most evident in mid-latitude ecoregions, where conditions for growth (reflected in actual evapotranspiration rates) are optimal. Away from this optimum, climate severity leads to non-significant height clustering in actual communities.</p>
Figs 7–8. Dineura Dahlbom, 1835, 3 in Descriptions and key to larvae of Central European Dineura (Hymenoptera: Symphyta: Tenthredinidae)
Figs 7–8. Dineura Dahlbom, 1835, 3rd abdominal segment of larvae (a – dorsal section, b – subspiracular lobe): 7 – D. stilata (Klug, 1816), 8 – D. testaceipes (Klug, 1816), 9 – D. virididorsata (Retzius, 1783). Scale bar: 0.05 mm.
Figs 4–6. Dineura Dahlbom, 1835 in Descriptions and key to larvae of Central European Dineura (Hymenoptera: Symphyta: Tenthredinidae)
Figs 4–6. Dineura Dahlbom, 1835, larvae (a – lateral view, b – dorsal view): 4 – D. stilata (Klug, 1816), 5 – D. testaceipes (Klug, 1816), 6 – D. virididorsata (Retzius, 1783). Scale bar: 10 mm.
Fig. 40 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Fig. 40. Diagram with definition of 6 stages of reduction of venation in brachypterous and wing polymorphic species of Sphaeroceridae (West Palaearctic only).
Fig. 39 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Fig. 39. Wings of Aptilotus species from Canary Islands. Successive sequence of reduction of veins in wings in particular endemic species. The numbers 2–6 refers to stages of reduction of venation as defined in Fig. 40. A. beckeri (Duda, 1918) from Tenerife, a macropterous species (top wing); A. avolans (Roháček & Papp, 1983) from La Palma (left bottom); A. gomerensis (Papp & Roháček, 1981) from La Gomera (middle bottom); A. franzi (Papp & Roháček, 1981) from Tenerife (right bottom above, stage 5); A. anapterus (Papp & Roháček, 1981) from La Palma (right bottom below, stage 6).
Fig. 38 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Fig. 38. Wings of Pteremis fenestralis (Fallén, 1820). Successive sequence of reduction of veins in wings with increasing brachyptery. The numbers 2–5 refers to stages of reduction of venation as defined in Fig. 40.
Figs. 31–34 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Figs. 31–34. Spelobia pseudonivalis (Dahl, 1909), wings. 31 – submacropterous male (Czech Republic: Nízký Jeseník Mts.– Slunečná Mt.); 32 – slightly brachypterous female (Czech Republic: Hrubý Jeseník – Kouty nad Desnou); 33 – typical brachypterous female (Czech Republic: Horní Benešov env.); 34 – strongly brachypterous female with dm-cu cross-vein lost (Czech Republic: Moravský kras – Babice). Scale: 0.5 mm. Photo by J. Roháček.
Figs. 35–37 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Figs. 35–37. Terrilimosina corrivalis (Villeneuve, 1918), male wings. 35 – almost macropterous (Romania: Banat, Sfânta Elena – Kulhavá skála); 36 – usual brachypterous (Slovakia: Bukovské vrchy Mts.– Stužica res.); 37 – strongly brachypterous (Slovakia: Poľana Mts.– Hrončecký Grúň res.). Scale: 0.5 mm. Photo by J. Roháček.
Figs. 15–17 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Figs. 15–17. Spelobia manicata (Richards, 1927), male wings. 15 – macropterous (Czech Republic: Třešť); 16 – submacropterous (Czech Republic: Hrubý Jeseník Mts. – Kouty nad Desnou); 17 – brachypterous (Czech Republic: Třešť – Pouště). Scale: 0.5 mm. Photo by J. Roháček.
Figs. 12–14 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Figs. 12–14. Phthitia (Collimosina) spinosa (Collin, 1930), female wings. 12 – macropterous (Czech Republic: Řásná nr. Telč); 13 – slightly brachypterous, with apical part of R2+3 lost; 14 – distinctly brachypterous (both Czech Republic: Úvalenské louky res. nr. Krnov). Scale: 0.5 mm. Photo by J. Roháček.
Figs. 28–30 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Figs. 28–30. Puncticorpus cribratum (Villeneuve, 1918), wings. 28 – submacropterous (Hungary: Síkfőkút); 29 – medium brachypterous, 30 – extremely brachypterous (both Slovakia: Vihorlat Mts.– Stakčín env.). Photo by J. Roháček.
Figs. 23–27 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Figs. 23–27. Pullimosina (Pullimosina) meijerei (Duda, 1918), wings. 23 – macropterous female (Czech Republic: Třešť); 24 – largest brachypterous female (Czech Republic: Kunětická hora Mt.); 25 – brachypterous male with part of CuA 1 lost; 26 – normal brachypterous male; 27 – brachypterous male with dm-cu cross-vein lost (all Czech Republic: Lednice – Kančí obora). Scale: 0.5 mm. Photo by J. Roháček.
Figs. 5–11 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Figs. 5–11. Crumomyia pedestris (Meigen, 1830), wings. 5 – macropterous female; 6 – submacropterous female (both Slovakia: Tatranská Kotlina – Šarpanec); 7 – large brachypterous female; 8 – medium brachypterous female; 9 – strongly brachypterous female; 10 – almost micropterous male (all Czech Republic: Úvalenské louky res. nr. Krnov); 11 – macropterous male with additional dm-cu cross-vein (Slovakia: Tatranská Kotlina – Šarpanec). Scale: 0.5 mm. Photo by J. Roháček.
Figs. 18–22 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Figs. 18–22. Pteremis fenestralis (Fallén, 1820), female wings. 18 – macropterous; 19 – atypical brachypterous with dm-cu present; 20 – typical brachypterous (= Borborus nivalis Haliday, 1833); 21 – brachypterous with terminal part of R2+3 lost; 22 – strongly brachypterous (all Czech Republic: Hrubý Jeseník Mts.– Rejvíz res.). Scale: 0.5 mm. Photo by J. Roháček.
Figs. 1–4. Wing polymorphic Sphaeroceridae. 1 in Wing polymorphism in European species of Sphaeroceridae (Diptera)
Figs. 1–4. Wing polymorphic Sphaeroceridae. 1 – Crumomyia pedestris (Meigen, 1830), brachypterous male, body length 3.4 mm (Czech Republic: Úvalenské louky res. nr. Krnov); 2 – Pteremis fenestralis (Fallén, 1820), brachypterous male, body length 1.5 mm (Czech Republic: Jizerské hory Mts.– Jizerka); 3–4 – Pullimosina (Pullimosina) meijerei (Duda, 1918): 3 – macropterous female, body length 1.6 mm (Slovakia: Muránska planina Mts. – Šarkanica res.); 4 – male with ambiguous wings, body length 1.45 mm (Slovakia: Muránska planina Mts. – Bobačka cave env.). Photos by J. Roháček.
Figs. 33-34 – male antennae. 33 in Revision of Central European species of the Aclista scutellaris complex (Hymenoptera: Diapriidae)
Figs. 33-34 – male antennae. 33 – Aclista pseudobitensis sp. nov.; 34 – A. pseudosoror sp. nov. Scale bar = 3.0 mm. – male fore tibia. 35 – A. angusta (Kieffer, 1909); 36 – A. scutellaris (Thomson, 1859). Scale bar = 0.5 mm.
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Allen Brain Atlas
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International Brain Laboratory public data
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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.