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67 results for “European mountains”
On following pages: 18. Omilteme Cottontail (Sylvilagus insonus); 19. Common Tapeti (Sylvilagus brasiliensis); 20 Cottontail (Sylvilagus dice); 23. Mexican Cottontail (Sylvilagus cunicularius); 24. Tres Marias Cottontail (Sylvilagus Robust Cottontail (Sylvilagus robustus); 28. Manzano Mountain Cottontail (Sylvilagus cognatus); 29. Hispid Hare (. Central American Tapeti (Sylvilagus gabbi); 21. Venezuelan Lowland Rabbit (Sylvilagus varynaensis), 22. Dice's graysoni); 25. Eastern Cottontail (Sylvilagus floridanus); 26. Appalachian Cottontail (Sylvilagus obscurus); 27. Caprolagus hispidus); 30. Bunyoro Rabbit (Poelagus marjorita); 31. European Rabbit (Oryctolagus cuniculus). in Leporidae
On following pages: 18. Omilteme Cottontail (Sylvilagus insonus); 19. Common Tapeti (Sylvilagus brasiliensis); 20 Cottontail (Sylvilagus dice); 23. Mexican Cottontail (Sylvilagus cunicularius); 24. Tres Marias Cottontail (Sylvilagus Robust Cottontail (Sylvilagus robustus); 28. Manzano Mountain Cottontail (Sylvilagus cognatus); 29. Hispid Hare (. Central American Tapeti (Sylvilagus gabbi); 21. Venezuelan Lowland Rabbit (Sylvilagus varynaensis), 22. Dice's graysoni); 25. Eastern Cottontail (Sylvilagus floridanus); 26. Appalachian Cottontail (Sylvilagus obscurus); 27. Caprolagus hispidus); 30. Bunyoro Rabbit (Poelagus marjorita); 31. European Rabbit (Oryctolagus cuniculus).
On following pages: 25. Ognev's Mole (Talpa ognevi); 26. Caucasian Mole (Talpa caucasica); 27. Levant Mole (Talpa 31. Iberian Mole (Talpa occidentalis); 32. European Mole (Talpa europaea); 33. Aquitanian Mole (Talpa aquitania); 34 Mole (Mogera wogura); 37. Small Japanese Mole (Mogera imaizumii); 38. Sado Mole (Mogera tokudae); 39. Echigo Mole (Mogera kanoana); 43. La Touche's Mole (Mogera latouchel); 44. Himalayan Mole (Euroscaptor micrurus); 45 (Euroscaptor klossi); 48. Kuznetsov's Mole (Euroscaptor kuznetsovi); 49. Orlov''s Mole (Euroscaptor orlovi); 50. Vietnamese (Euroscaptor malayanus); 53. White-tailed Mole (Parascaptor leucurus); 54. Short-faced Mole (Scaptochirus moschatus levantis); 28. Balkan Mole (Talpa stankovici); 29. Blind Mole (Talpa caeca); 30. Roman Mole (Talpa romana);. Japanese Mountain Mole (Oreoscaptor mizura); 35. Ussuri Mole (Mogera robusta); 36. Large Japanese Mole (Mogera etigo); 40. Senkaku Mole (Mogera uchidai); 41. Insular Mole (Mogera insularis); 42. Kano's . Greater Chinese Mole (Euroscaptor grandis); 46. Long-nosed Mole (Euroscaptor longirostris); 47. Kloss's Mole Mole (Euroscaptor subanura); 51. Small-toothed Mole (Euroscaptor parvidens); 52. Malaysian Mole). in Talpidae
On following pages: 25. Ognev's Mole (Talpa ognevi); 26. Caucasian Mole (Talpa caucasica); 27. Levant Mole (Talpa 31. Iberian Mole (Talpa occidentalis); 32. European Mole (Talpa europaea); 33. Aquitanian Mole (Talpa aquitania); 34 Mole (Mogera wogura); 37. Small Japanese Mole (Mogera imaizumii); 38. Sado Mole (Mogera tokudae); 39. Echigo Mole (Mogera kanoana); 43. La Touche's Mole (Mogera latouchel); 44. Himalayan Mole (Euroscaptor micrurus); 45 (Euroscaptor klossi); 48. Kuznetsov's Mole (Euroscaptor kuznetsovi); 49. Orlov''s Mole (Euroscaptor orlovi); 50. Vietnamese (Euroscaptor malayanus); 53. White-tailed Mole (Parascaptor leucurus); 54. Short-faced Mole (Scaptochirus moschatus levantis); 28. Balkan Mole (Talpa stankovici); 29. Blind Mole (Talpa caeca); 30. Roman Mole (Talpa romana);. Japanese Mountain Mole (Oreoscaptor mizura); 35. Ussuri Mole (Mogera robusta); 36. Large Japanese Mole (Mogera etigo); 40. Senkaku Mole (Mogera uchidai); 41. Insular Mole (Mogera insularis); 42. Kano's . Greater Chinese Mole (Euroscaptor grandis); 46. Long-nosed Mole (Euroscaptor longirostris); 47. Kloss's Mole Mole (Euroscaptor subanura); 51. Small-toothed Mole (Euroscaptor parvidens); 52. Malaysian Mole).
On following pages: 79. Eastern Mole Vole (Ellobius tancrei); 80. Alai Mole Vole (Ellobius alaicus); 81. Southern Mole Vole (Ellobius fuscocapillus); 82. Transcaucasian Mole Vole (Ellobius lutescens); 83. Yellow Steppe Lemming (Eolagurus luteus); 84. Przewalski's Steppe Lemming (Eolagurus przewalskii); 85. Steppe Vole (Lagurus lagurus), 86. South-western Water Vole (Arvicola sapidus); 87. Eurasian Water Vole (Arvicola amphibius); 88. Montane Water Vole (Arvicola monticola); 89. Italian Water Vole (Arvicola italicus); 90. Sagebrush Vole (Lemmiscus curtatus); 91. European Snow Vole (Chionomys nivalis); 92. Robert's Snow Vole (Chionomys robert); 93. Gudaur Snow Vole (Chionomys gud); 94. Lazistan Snow Vole (Chionomys lasistanius); 95. Sichuan Vole (Volemys millicens); 96. Marie's Vole (Volemys musseri); 97. Duke of Bedford's Vole (Proedromys bedford); 98. Liangshan Vole (Proedromys liangshanensis); 99. Brandt's Vole (Lasiopodomys brandftil); 100. Mandarin Vole (Lasiopodomys mandarinus); 101. Narrow-headed Vole (Lasiopodomys gregalis); 102. Radde's Vole (Lasiopodomys raddei); 103. Sikkim Mountain Vole (Neodon sikimensis); 104. Linzhi Mountain Vole (Neodon linzhiensis); 105. Clarke's Vole (Neodon clarke); 106. Medog Mountain Vole (Neodon medogensis); 107. Nyalam Mountain Vole (Neodon nyalamensis); 108. Irene Mountain Vole (Neodon irene); 109. Forrest's Mountain Vole (Neodon forresti); 110. Blyth's Mountain Vole (Neodon leucurus); 111. Smoky Mountain Vole (Neodon fuscus). in Cricetidae
On following pages: 79. Eastern Mole Vole (Ellobius tancrei); 80. Alai Mole Vole (Ellobius alaicus); 81. Southern Mole Vole (Ellobius fuscocapillus); 82. Transcaucasian Mole Vole (Ellobius lutescens); 83. Yellow Steppe Lemming (Eolagurus luteus); 84. Przewalski's Steppe Lemming (Eolagurus przewalskii); 85. Steppe Vole (Lagurus lagurus), 86. South-western Water Vole (Arvicola sapidus); 87. Eurasian Water Vole (Arvicola amphibius); 88. Montane Water Vole (Arvicola monticola); 89. Italian Water Vole (Arvicola italicus); 90. Sagebrush Vole (Lemmiscus curtatus); 91. European Snow Vole (Chionomys nivalis); 92. Robert's Snow Vole (Chionomys robert); 93. Gudaur Snow Vole (Chionomys gud); 94. Lazistan Snow Vole (Chionomys lasistanius); 95. Sichuan Vole (Volemys millicens); 96. Marie's Vole (Volemys musseri); 97. Duke of Bedford's Vole (Proedromys bedford); 98. Liangshan Vole (Proedromys liangshanensis); 99. Brandt's Vole (Lasiopodomys brandftil); 100. Mandarin Vole (Lasiopodomys mandarinus); 101. Narrow-headed Vole (Lasiopodomys gregalis); 102. Radde's Vole (Lasiopodomys raddei); 103. Sikkim Mountain Vole (Neodon sikimensis); 104. Linzhi Mountain Vole (Neodon linzhiensis); 105. Clarke's Vole (Neodon clarke); 106. Medog Mountain Vole (Neodon medogensis); 107. Nyalam Mountain Vole (Neodon nyalamensis); 108. Irene Mountain Vole (Neodon irene); 109. Forrest's Mountain Vole (Neodon forresti); 110. Blyth's Mountain Vole (Neodon leucurus); 111. Smoky Mountain Vole (Neodon fuscus).
On following pages: 223. Mohave Ground Squirrel (Xerospermophilus mohavensis); 224. Perote Ground Squirrel (Xerospermophilus perotensis); 225. Ring-tailed Ground Squirrel (Notocitellus annulatus); 226. Tropical Ground Squirrel (Notocitellus adocetus); 227. European Ground Squirrel (Spermophilus citellus); 228. Russet Ground Squirrel (Spermophilus major); 229. Speckled Ground Squirrel (Spermophilus suslicus); 230. Yellow Ground Squirrel (Spermophilus fulvus); 231. Little Ground Squirrel (Spermophilus pygmaeus); 232. Caucasian Mountain Ground Squirrel (Spermophilus musicus); 233. Asia Minor Ground Squirrel (Spermophilus xanthoprymnus); 234. Tauren Ground Squirrel (Spermophilus taurensis); 235. Red-cheeked Ground Squirrel (Spermophilus erythrogenys); 236. Relict Ground Squirrel (Spermophilus relictus); 237. Tian Shan Ground Squirrel (Spermophilus nilkaensis); 238. Brandt's Ground Squirrel (Spermophilus brevicauda); 239. Pallid Ground Squirrel (Spermophilus pallidicauda); 240. Alashan Ground Squirrel (Spermophilus alashanicus); 241. Daurian Ground Squirrel (Spermophilus dauricus). in Sciuridae
On following pages: 223. Mohave Ground Squirrel (Xerospermophilus mohavensis); 224. Perote Ground Squirrel (Xerospermophilus perotensis); 225. Ring-tailed Ground Squirrel (Notocitellus annulatus); 226. Tropical Ground Squirrel (Notocitellus adocetus); 227. European Ground Squirrel (Spermophilus citellus); 228. Russet Ground Squirrel (Spermophilus major); 229. Speckled Ground Squirrel (Spermophilus suslicus); 230. Yellow Ground Squirrel (Spermophilus fulvus); 231. Little Ground Squirrel (Spermophilus pygmaeus); 232. Caucasian Mountain Ground Squirrel (Spermophilus musicus); 233. Asia Minor Ground Squirrel (Spermophilus xanthoprymnus); 234. Tauren Ground Squirrel (Spermophilus taurensis); 235. Red-cheeked Ground Squirrel (Spermophilus erythrogenys); 236. Relict Ground Squirrel (Spermophilus relictus); 237. Tian Shan Ground Squirrel (Spermophilus nilkaensis); 238. Brandt's Ground Squirrel (Spermophilus brevicauda); 239. Pallid Ground Squirrel (Spermophilus pallidicauda); 240. Alashan Ground Squirrel (Spermophilus alashanicus); 241. Daurian Ground Squirrel (Spermophilus dauricus).
Distribution. Widespread in Europe (from Iceland, Britain, and Iberia E to S Norway, S Sweden, Belarus, SW European Russia, E Ukraine, and the Balkan Peninsula) and in coastal and mountainous regions of Morocco, Algeria, and Tunisia. in Muridae
Distribution. Widespread in Europe (from Iceland, Britain, and Iberia E to S Norway, S Sweden, Belarus, SW European Russia, E Ukraine, and the Balkan Peninsula) and in coastal and mountainous regions of Morocco, Algeria, and Tunisia.
Supplementary material 4 from: Boenigk J, Wodniok S, Bock C, Beisser D, Hempel C, Grossmann L, Lange A, Jensen M (2018) Geographic distance and mountain ranges structure freshwater protist communities on a European scalе. Metabarcoding and Metagenomics 2: e21519. https://doi.org/10.3897/mbmg.2.21519
Richness is shown for different elevations. The number of lakes within this elevation range is indicated. While mean richness ranges around 750 OTUs it drops to around 400 OTUs at high elevations. The transition seems to be around or slightly below 1400m.
Fig. 1 in Species radiation in the Alps: multiple range shifts caused diversification in Ringlet butterflies in the European high mountains
Fig. 1 Sampling locations of all studied species, with Erebia cassioides arvernensis (grey circles), Erebia c. cassioides (black circles), Erebia c. neleus in the Balkan region (black-white circles), Erebia nivalis (white triangles), Erebia tyndarus (white circles) and Erebia ottomana (grey triangles) (a). The detailed map shows the distribution of the samples in the Alps (b). Given numbers coincide with other figures and tables
FIGURE 2 in Underestimated diversity in one of the world's best studied mountain ranges: The polyploid complex of Senecio carniolicus (Asteraceae) contains four species in the European Alps
FIGURE 2. Representative shapes of rosette leaves (left) and cauline leaves (right) of Senecio carniolicus (A) and S. noricus (B). Drawings: R. Flatscher.
FIGURE 3 in Underestimated diversity in one of the world's best studied mountain ranges: The polyploid complex of Senecio carniolicus (Asteraceae) contains four species in the European Alps
FIGURE 3. Representative shapes of rosette leaves (left) and cauline leaves (right) of Senecio insubricus (A) and S. disjunctus (B). Drawings: R. Flatscher.
FIGURE 1 in Underestimated diversity in one of the world's best studied mountain ranges: The polyploid complex of Senecio carniolicus (Asteraceae) contains four species in the European Alps
FIGURE 1. Iconography of Senecio carniolicus (A), S. insubricus (B), S. noricus (C) and S. disjunctus (D). Drawings: R. Flatscher.
FIGURE 4 in Underestimated diversity in one of the world's best studied mountain ranges: The polyploid complex of Senecio carniolicus (Asteraceae) contains four species in the European Alps
FIGURE 4. Representative individuals of Senecio carniolicus (A, Almerhorn, population 58 from Sonnleitner et al. 2010), S. insubricus (B; Plose, population 46), S. noricus (C; Bretthöhe, population 80), and S. disjunctus (D; Bretthöhe, population 80). Note the characteristic differences in indumentum density and leaf dissection as well as in the number of capitula per synflorescence. Photographs: M. Sonnleitner.
FIGURE 5 in Underestimated diversity in one of the world's best studied mountain ranges: The polyploid complex of Senecio carniolicus (Asteraceae) contains four species in the European Alps
FIGURE 5. Distribution of the four species of the Senecio carniolicus agg. in the Eastern Alps based on Sonnleitner et al. (2010); S. carniolicus (A), S. insubricus (B), S. noricus (C) and S. disjunctus (D). Morphometrically evaluated populations are marked with a black dot.
Data from: Genetic differentiation of western capercaillie in the Carpathian Mountains reveal the importance of post glacial expansions and habitat connectivity in understanding the present day European distribution
Population structure and barriers to gene flow are important components for understanding the evolutionary history of a species. Here we study population structure and differentiation in the western capercaillie (Aves: Phasianidae) along the Carpathian Mountains. Further, we compared the levels of population differentiation among capercaillie from the Carpathian Mountains, Balkans (Bulgaria) and the boreal forest (Russia and Sweden) in order to reveal past and current processes which may influence population structure. Tissue samples, non-invasive faeces and feathers and toe pads from museum specimens were used for genetic analyses of mitochondrial (mtDNA) sequences and allelic variation at nine nuclear DNA (nDNA) microsatellite loci. Analyses of mtDNA sequences revealed a southern subclade within the northern clade. Within the northern clade, microsatellite data distinguished two groups: (1) Western Carpathian populations; and (2) Eastern Carpathian and boreal forest populations. Bulgarian populations constituted a third cluster corresponding to the southern phylogenetic subclade. The Western Carpathian populations showed a heterozygote deficiency. The analyses indicate that the abundant Eastern Carpathian populations share alleles with populations from the boreal forest suggesting a common origin of these populations since the last glacial period. On the other hand, the Western Carpathian populations have been isolated over a long period with only a few migrants from the east, thereby becoming differentiated from the eastern and northern populations. The southern populations have been isolated from the northern populations since the last glacial maximum. The molecular analyses did not support the currently recognised taxonomy at the subspecies level.
Figure 3 in Congruent patterns of lineage diversity in two species complexes of planktonic crustaceans, Daphnia longispina (Cladocera) and Eucyclops serrulatus (Copepoda), in East European mountain lakes
Figure 3. Relationship of eight clades of the Eucyclops serrulatus complex, assessed by Bayesian inference of phylogeny, and haplotype variation of the 12S rRNA gene within clade I. The phylogenetic tree was based on the 1299-bp-long alignment consisting of fragments of mitochondrial genes for 12S rRNA and cytochrome b, and the nuclear gene for 18S rRNA. The scale bar represents genetic distance; numbers at nodes indicate branch support (as posterior probabilities). Haplotype network representing the variation within clade I is based on 43 sequences of the 383-bp-long 12S rDNA fragment. Individuals from the three main mountain regions are indicated by different shading (as in Figs 1, 2) in both tree and network: the Carpathians in dark grey (N = 24), Macedonian-Thracian massif in white (N = 9), and Dinaric Alps in light grey (N = 26). Mountain range abbreviations: Bje, Bjelasica; Dur, Durmitor; Pir, Pirin; Pro, Prokletije; Ret, Retezat; Ril, Rila; Sar, Šar Planina; Tat, Tatra Mountains; Tre, Treskavica; Zel, Zelengora. Countries are indicated by two-letter codes (see Table 1).
Figure 2 in Congruent patterns of lineage diversity in two species complexes of planktonic crustaceans, Daphnia longispina (Cladocera) and Eucyclops serrulatus (Copepoda), in East European mountain lakes
Figure 2. Sequence variation of the 528-bp-long fragment of the 12S rRNA gene within the Daphnia longispina complex from lakes of the studied East European mountain ranges. This is shown in a maximum likelihood tree (A) consisting only of sequences from the studied region (each haplotype represented once per lake), and in a parsimony network (B) of haplotypes of D. longispina s.s., amongst which 63 reference sequences from other European localities were also included. Three main mountain regions from this study are differentiated by shading: the Carpathians in dark grey, Macedonian-Thracian massif in white, and Dinaric Alps in light grey. Haplotypes from other localities, only included in the network, are enclosed by dashed lines. Mountain range abbreviations: Bje, Bjelasica; Dur, Durmitor; Pir, Pirin; Pro, Prokletije; Ret, Retezat; Ril, Rila; Tat, Tatra Mountains; Tre, Treskavica; Zel, Zelengora. Countries are indicated by two-letter codes (see Table 1).
Figure 1 in Congruent patterns of lineage diversity in two species complexes of planktonic crustaceans, Daphnia longispina (Cladocera) and Eucyclops serrulatus (Copepoda), in East European mountain lakes
Figure 1. Map of the sampled Eastern European mountain ranges (Bje, Bjelasica; Dur, Durmitor; Pir, Pirin; Pro, Prokletije; Ret, Retezat; Ril, Rila; Sar, Šar Planina; Tat, Tatra Mountains; Tre, Treskavica; Zel, Zelengora). The main mountain regions are differentiated by shading: the Carpathians in dark grey, Macedonian-Thracian massif in white, and Dinaric Alps in light grey. Countries are indicated by two-letter codes (see Table 1).
Data from: Future ecosystem services from European mountain forests under climate change
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Data from: Polyploidisation and geographic differentiation drive diversification in a European high mountain plant group (Doronicum clusii aggregate, Asteraceae)
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Data from: Genetic differentiation of western capercaillie in the Carpathian Mountains reveal the importance of post glacial expansions and habitat connectivity in understanding the present day European distribution
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Schistidium foraminis-martini sp. nov. (Grimmiaceae), a high mountain calcicole from the European Alps molecularly related to S. agassizii
<p>Alignment of the ITS region of accessions of Schistidium and Grimmia (Bryophyta).</p>
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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.