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FIGURE 4 in Taraxacum sect. Erythrocarpa in Europe in the Alps and eastwards: A revision of a precursor group of relicts
FIGURE 4. Distribution of species of T. sect. Erythrocarpa. Taraxacum fastuosum (squares), T. adamovicii (star), T. olympophilum (green/dark circles), T. pieninicum (yellow/light circles).
Subspecies and Distribution. L. t. timidus Linnaeus, 1758 — Scandinavia S to 59° N, N Russia (S to 57° N to 58° N) to E of Ural Mts, Estonia, perhaps Poland, and Altai and Beita Mts in N Xinjiang (China); from Sweden extending in hybrid zones with the subspecies sylvaticus to S coast of Norway and W Latvia. L. t. abet Kuroda, 1938 — Kurile Is (Russia). L. t. ainu Barrett-Hamilton, 1900 — Hokkaido (Japan). L. t. begitschevi Koljuschev, 1936 — Taimyr Peninsula (Russia). L. t. gichiganus J. A. Allen, 1903 — C Yakutia, Kamchatka and Okhotsk Sea coast (Russia). L. t. hibernicus Bell, 1837 — Ireland. L. t. kolymensis Ognev, 1922 — NE Siberia (Russia). L. t. kozhevnikovi Ognev, 1929 — C Russia from 57° to 58°N, whereit intergrades with the nomonotypical timidus S to 53° N. The W boundary is unclear. L. t. lugubris Kastschenko, 1899 — Siberian Altai Mts (Russia). L. t. mordeni Goodwin, 1933 — Russian Far East (Ussuri Valley and lower and middle Amur River) and Heilongjiang (China). L. t. ori Kuroda, 1928 — Sakhalin (Russia). L. t. scoticus Hilzheimer, 1906 — Scotland. L. t. sibiricorumJohansen, 1923 — W & SW Siberia (Russia), N Kazakhstan, and Tacheng Mts in N Xinjiang (China). L. t. sylvaticus Nilsson, 1831 —S Sweden, extending in hybrid zones with nominotypical timidus to S coast of Norway and W Latvia. L. t. transbaikalicus Ognev, 1929 — Trans-Baikal region in E Siberia (Russia) and E Inner Mongolia (= Nei Mongol, China). L. t. varronis Miller, 1901 — at high altitudes in the Alps, C Europe. in Leporidae
Subspecies and Distribution. L. t. timidus Linnaeus, 1758 — Scandinavia S to 59° N, N Russia (S to 57° N to 58° N) to E of Ural Mts, Estonia, perhaps Poland, and Altai and Beita Mts in N Xinjiang (China); from Sweden extending in hybrid zones with the subspecies sylvaticus to S coast of Norway and W Latvia. L. t. abet Kuroda, 1938 — Kurile Is (Russia). L. t. ainu Barrett-Hamilton, 1900 — Hokkaido (Japan). L. t. begitschevi Koljuschev, 1936 — Taimyr Peninsula (Russia). L. t. gichiganus J. A. Allen, 1903 — C Yakutia, Kamchatka and Okhotsk Sea coast (Russia). L. t. hibernicus Bell, 1837 — Ireland. L. t. kolymensis Ognev, 1922 — NE Siberia (Russia). L. t. kozhevnikovi Ognev, 1929 — C Russia from 57° to 58°N, whereit intergrades with the nomonotypical timidus S to 53° N. The W boundary is unclear. L. t. lugubris Kastschenko, 1899 — Siberian Altai Mts (Russia). L. t. mordeni Goodwin, 1933 — Russian Far East (Ussuri Valley and lower and middle Amur River) and Heilongjiang (China). L. t. ori Kuroda, 1928 — Sakhalin (Russia). L. t. scoticus Hilzheimer, 1906 — Scotland. L. t. sibiricorumJohansen, 1923 — W & SW Siberia (Russia), N Kazakhstan, and Tacheng Mts in N Xinjiang (China). L. t. sylvaticus Nilsson, 1831 —S Sweden, extending in hybrid zones with nominotypical timidus to S coast of Norway and W Latvia. L. t. transbaikalicus Ognev, 1929 — Trans-Baikal region in E Siberia (Russia) and E Inner Mongolia (= Nei Mongol, China). L. t. varronis Miller, 1901 — at high altitudes in the Alps, C Europe.
FIGURES 47-54 in Comparative larval ultramorphology of three endemic Lathrobium (Glyptomerus) species (Coleoptera, Staphylinidae, Paederinae) from the Eastern Alps in Italy
FIGURES 47-54. Mature larva of L. alzonai (47, 47A, 48, 51, 52), L. freyi (49, 53) and L. pacei (50, 54). 47-54, right maxilla with stipes (48), microstructure near trichobothrium (51) and region of mala (52-54) in ventral aspect. Abbreviations: Cd— cardo, Pf—palpifer, Ma—mala, I-III—antennal and maxillary palp articles, St—stipes, Trb—trichobothrium, 1, 2—setae of maxillary palp.
Figure 5 in Shedding light on species boundaries in small endogeic animals through an integrative approach: species delimitation in the centipede Clinopodes carinthiacus (Chilopoda: Geophilidae) in the south-eastern Alps
Figure 5. Contribution of the bioclimatic variables on the first two principal components of climatic variation in the study area, and density of occurrence of Clinopodes carinthiacus s.s. and Clinopodes strasseri on the two principal components estimated with ecospat, based on 106 sites (former species) and 16 sites (latter). Continuous and dashed contour lines indicate 100% and 50% of the available climatic space, respectively.
Fig. 4 Zospeum spelaeum. a lectotype SMF 158543 in An integrative taxonomic study reveals carychiid microsnails of the troglobitic genus Zospeum in the Eastern and Dinaric Alps (Gastropoda, Ellobioidea, Carychiinae)
Fig. 4 Zospeum spelaeum. a lectotype SMF 158543, Postojnska jama, sh: 1.634 mm. — b1–6 NMBE 553308, Betalov Spodmol, sh: 1.8 mm; c ditto, sh: 1.495 mm. — d NMBE 553306, Betalov Spodmol, sh: 1.8 mm. — e NMBE 553310, Mačkovica jama, sh: 2.39 mm. — f1–2 NMBE 553312, Velika Pasica, sh: 2.055 mm. —(g) NMBE 553311, sh: 1.957 mm; h ditto, sh: 2.07 mm. — i NMBE 553304, Čampari jama,
Fig. 2 in An integrative taxonomic study reveals carychiid microsnails of the troglobitic genus Zospeum in the Eastern and Dinaric Alps (Gastropoda, Ellobioidea, Carychiinae)
Fig. 2 Top: The nine measurements as illustrated on the frontal (left) and apical (right) view of a Zospeum manitaense shell (NMBE 549731). Bottom right: Position of the 14 landmarks on the shell. Bottom left: Nomenclature to dentition indicated on shell of Zospeum lamellatum (MCSMNH 35995)
Fig. 6 in An integrative taxonomic study reveals carychiid microsnails of the troglobitic genus Zospeum in the Eastern and Dinaric Alps (Gastropoda, Ellobioidea, Carychiinae)
Fig. 6 (a–e) Zospeum alpestre, (a1–2) NHMW 75000 (E 12483), Dovja griča, sh: 1.485 mm; (b) ditto, sh: 1.369 mm; (c1–2) ditto, sh: 1.432 mm. — (d1–2) NMBE 553373, Jama pod Mokrico, sh: 1.652 mm. — (e) SMNH 2216, Jama pod Mokrico, sh: 1.53 mm. —(f–i) Zospeum kupitzense, (f) Holotype, SMF 256354, Kupitzklamm, sh: 1.67 mm. — (g1–2) Paratype, NMBE 549730, sh: 1.551 mm; (h) ditto, sh: 1.536 mm. — (i1–2) NMBE 553393, Ložekarjeva jama, sh: 1.657 mm. —(j–k) Zospeum isselianum, (j1–2) Neotype, MCSMNH 37013, Turjeva jama,
Fig. 1 a in An integrative taxonomic study reveals carychiid microsnails of the troglobitic genus Zospeum in the Eastern and Dinaric Alps (Gastropoda, Ellobioidea, Carychiinae)
Fig. 1 a Currently known distribution of the genus Zospeum in the southwestern Alps and the Dinarids; b Distribution of recovered clades
Fig. 5 a–f in An integrative taxonomic study reveals carychiid microsnails of the troglobitic genus Zospeum in the Eastern and Dinaric Alps (Gastropoda, Ellobioidea, Carychiinae)
Fig. 5 a–f Zospeum costatum, (a) NHMW 71848, Babja luknja, Goričane, sh: 2.214 mm; (b) ditto, sh: 2.043 mm. — (c1–3) NHMW 71847, Babja luknja, Goričane, sh: 2.08 mm. — (d) NMBE 553383, Jama 2 pri Jabljah, sh: 1.86 mm; (e) ditto, sh: 1.92 mm; (f) ditto, sh: 2.03 mm. —(g–k) Zospeum lamellatum, (g1–3) Lectotype, MCSMNH 35995, Krasnica, sh: 2.059 mm. — (h) MCSMNH 7057, Ukovnik pri sp. Idriji, sh: 1.751 mm; (i) ditto, sh: 1.739 mm; (j) ditto, sh: 1.733 mm; (k) ditto, sh: 1.766 mm. —(l–m) Zospeum lautum, (l1–2) NHMW 71828,
Fig. 2 Neighbour-joining phenogram calculated with the program PHYLIP ver. 3.5.c in Species radiation in the Alps: multiple range shifts caused diversification in Ringlet butterflies in the European high mountains
Fig. 2 Neighbour-joining phenogram calculated with the program PHYLIP ver. 3.5.c. (Felsenstein 1993), based on Nei's (1972) genetic distances for all samples analysed. The tree topology assigned the samples into the following six main clusters (from left to right): Erebia tyndarus (Central Alps), Erebia c. neleus (Balkans and Retezat), Erebia ottomana (Balkans), Erebia c. cassioides (eastern Alps with Apennines), Erebia c. arvernensis (western Alps, Pyrenees, Massif Central and Passo Maghen located in the south-eastern Alps) and Erebia nivalis (eastern Alps). Bootstrap values calculated with 1000 permutations are given for values exceeding 50 % probability
Dataset Bert et al 2024 Diatom assemblages in glacial-fed streams of Italian Western Alps
<p>Dataset on diatoms collected in glacial-fed rivers of Northern Italy. Please refer to the following citation for details on methods:</p> <p> </p> <p><strong><span> </span></strong></p> <p><strong><span>Bert M., Falasco E., Mobili L. , Piovano S , Bona F. </span></strong></p> <p><strong><span>Diatom assemblages in glacial-fed streams of Italian Western Alps (submitted to Botany Letters)</span></strong></p> <p> </p> <p><span>if you use this database for research purposes, cite this paper</span></p>
Figure 4 in A dark shell hiding great variability: a molecular insight into the evolution and conservation of melanic Daphnia populations in the Alps
Figure 4. Unrooted haplotype networks of European Daphnia pulicaria haplotypes showing disconnections at the 97% parsimony threshold. Different patterns identify the main haplogroups considered in this study (see Fig. 1 for geographical distributions of haplogroups). Circles indicate distinct haplotypes (size proportional to the number of specimens sharing the same haplotype). Bold outlines indicate haplotypes found in our melanic alpine populations. The minimum number of mutational steps required to connect all haplotypes in a single network is also given (dashed double-arrowed lines). Alpine haplotypes are coded as in Fig. 3. Black dots indicate missing (unsampled/extinct) haplotypes.
FIGURE 17 in A new species in the Simulium vernum group from the Northern Limestone Alps of Austria: Simulium hasekei (Diptera: Simuliidae)
FIGURE 17. Chromosome arm IIIL, plus base of IIIS, of female larva of Simulium hasekei n. sp. from the type locality, showing the IIIL-1,9,37 sequence. Numbers above the chromosome are section numbers corresponding to the standard sequence of Brockhouse (1985). Numbers 1 to 8 below the chromosome correspond with those of Hunter (2002); arranging them in numerical sequence from 1 to 8 will provide the stepwise transition to the standard sequence for the S. vernum group. Breakpoints of inversions IIIL-9 and IIIL-37 are indicated with arrows below the chromosome; the breakpoints of IIIL-1 would be apparent before IIIL-9 and IIIL-37 occurred. C, centromere.
BMP-2 and ALP Levels Following Laser Therapy With Scaling and Root Planing in Periodontitis- RCT.
ClinicalTrials.gov study NCT05555420. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Endothelial SRSF1 directly regulates ATF3-KLF2 pathway to promote ischemia-induced angiogenesis [ALP_RNA-seq]
GEO Series GSE285367. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Apuan Alps floristic dataset
<p>This dataset has been realized starting from the flora of Apuan Alps ("Prodromo alla flora della Regione Apuana" Ferrarini & Marchetti 1994, Ferrarrini et al. 1997, Ferrarrini 2000) and has been analysed in Di Musciano et al. (under review on Frontiers in Biogeography).</p>
Figure 6 in Grasshoppers in winter: adults observed in a xerothermic oasis in the Italian Alps
Figure 6. Mating of Pezotettix giornae (9 February 2019).
Figure 3 in Grasshoppers in winter: adults observed in a xerothermic oasis in the Italian Alps
Figure 3. Total abundance of specimens sampled in the two years of monitoring.
FIGURE 22. Taraxacum calocephalum. A in Taraxacum sect. Erythrocarpa in Europe in the Alps and eastwards: A revision of a precursor group of relicts
FIGURE 22. Taraxacum calocephalum. A, Achenes (PRA, no. det. 16007). B, Geographical distribution.
Znaki i inna infrastruktura z zakresu informacji turystycznej w wybranych obszarach ochrony ciemnego nieba w Europie Zachodniej (RCN Cranborne Chase, RCN Alpes Azur Mercantour, PCN Galloway Forest)
<p>Dane zawierają zdjęcia w formacie jpg, wykonane w 2022 r. w trakcie realizacji grantu badawczego MINIATUA 5 NCN "Ocena promocji parków ciemnego nieba w ramach systemów informacji turystycznej na szczeblu regionalnym i lokalnym w Polsce i wybranych krajach Europy". Zdjęcia przedstawiają wybraną infrastrukturę informacji turystycznej w wybranych obszarach ciemnego nieba i ich okolicy (RCN Cranborne Chase, RCN Alpes Azur Mercantour, PCN Galloway Forest). Dane nie zawierają danych wrażliwych</p>
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OpenNeuro
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