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Fig. 3 in A vanishing hotspot-the impact of molecular insights on the diversity of Central European Bythiospeum Bourguignat, 1882 (Mollusca: Gastropoda: Truncatelloidea)
Fig. 3 Maximum likelihood phylogenetic tree of the 35 Bythiospeum populations based on 191 partial COI sequences; numbers at the nodes show bootstrap support, branches and tips with bootstrap support <75 collapsed. Grey squares delineate the discussed clades
Fig. 8 in A vanishing hotspot-the impact of molecular insights on the diversity of Central European Bythiospeum Bourguignat, 1882 (Mollusca: Gastropoda: Truncatelloidea)
Fig. 8 Variation of penis morphology in clade III. A, B Dossenbach, SMNS-ZI0059269/59268. C, D Boncourt, SMNS-ZI0079874/79878. E Source de la Serrière, SMNS-ZI0079803. F, G Source de la Douay, SMNS-ZI0079818/79826. H, I Interlaken, SMNS-ZI0098583-04/-15. Scale bar: 0.5 mm
Fig. 6 in A vanishing hotspot-the impact of molecular insights on the diversity of Central European Bythiospeum Bourguignat, 1882 (Mollusca: Gastropoda: Truncatelloidea)
Fig. 6 Variation in female anatomy in clade I—intestinal loop and complex of oviduct, bursa copulatrix and receptaculum seminis. Alz, BOE 2818 (A, F). Achenwald, BOE 1212 (B, G). Isar-Munich/Au, BOE 3333 (C). Hinterfallbach, BOE 1133 (D), BOE 1095 (H). Schwangau, BOE 1207 (E, I). Wernau, BOE 1176 (J). Abbreviations: bc, bursa copulatrix; in, intestine; ov, oviduct; rs, receptaculum seminis. Scale bar: 0.5 mm
Figs 106–122. 106–110 in New and interesting records of Auchenorrhyncha (Homoptera) in European Russia
Figs 106–122. 106–110 — Handianus fartilis; 111–114 — Paralimnus elegans; 115–119 — Calamotettix taeniatus; 120–122 — Sorhoanus (Emeljanovianus) magnus. 106, 114–115 — habitus, dorsal view; 107, 116, 120 — pygofer and anal tube, ventral view; 108, 117 — male genitalia, pygofer removed, dorsal view; 109, 112, 118, 121 — aedeagus, lateral view; 110, 113, 119, 122 — same, back view; 111 — male abdominal apodemes. Рис. 106–122. 106–110 — Handianus fartilis; 111–114 — Paralimnus elegans; 115–119 — Calamotettix taeniatus; 120–122 — Sorhoanus (Emeljanovianus) magnus. 106, 114–115 — внеШний вид, сверху; 107, 116, 120 — пигофор и анальнаЯ трубка, сниЗу; 108, 117 — гениталии самца, сверху, пигофор удален; 109, 112, 118, 121 — Эдеагус, сбоку; 110, 113, 119, 122 — то же, сЗади; 111 — брюШные аподемы самца.
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
Fig. 1 a–d in Climatic correlates of body size in European tenebrionid beetles (Coleoptera: Tenebrionidae)
Fig. 1 a–d Relationships between latitude and mean body length of tenebrionid faunas in European countries. Both OLS and SAR regression lines are shown. Equation parameters are reported here only for OLS regressions. SAR parameters are given in Table 3 a All species (y = −0.1865x+17.695, R 2 =0.7256). b Endemics (y =0.4527x −9.7867, R 2 =0.3526). c Pimeliinae (y =−0.107x+16.157, R 2 =0.0238). d Non Pimeliinae (y =−0.1489x+15.59, R 2 =0.7246). Dotted lines OLS regressions. Solid lines SAR regressions
Fig. 3 in Genetic differentiation of the African dwarf crocodile Osteolaemus tetraspis Cope, 1861 (Crocodylia: Crocodylidae) and consequences for European zoos
Fig. 3 Haplotype networks of nuclear RAG-1 and LDH-A gene sequences (a) and mitochondrial COI, cyt-b/CR and 12S genes (b) from 33 African dwarf crocodiles from zoological gardens in Europe. Numbers of individuals with identical sequences are indicated within
Fig. 8 in Phylogeny, classification and taxonomy of European dragonflies and damselflies (Odonata): a review
Fig. 8 Phylogeny of Leucorrhinia (one monophyletic North American group not given in detail), based on Hovmöller and Johansson (2004). The taxa occur in the Eastern Palaearctic (EP), Nearctic (NA) or Western Palaearctic (WP)
Fig. 6 in Phylogeny, classification and taxonomy of European dragonflies and damselflies (Odonata): a review
Fig. 6 Inferred phylogeny of European 'higher' Libelluloidea, based on Ware et al. (2007), Pilgrim and von Dohlen (2008) and Fleck et al. (2008a, b). These trees only show groups' relative positions, but provide no estimate of their relatedness (i.e. shorter branch lengths do not indicate more recent shared ancestry)
Fig. 4 in The symbiotic hesionid Parasyllidea humesi Pettibone, 1961 (Annelida: Polychaeta) hosted by Scrobicularia plana (da Costa, 1778) (Mollusca: Bivalvia: Semelidade) in European waters
Fig. 4 Scrobicularia plana (Da Costa 1778). a Percentages of infested and non-infested specimens according to the size classes (shell length in mm) (n 02,373). b Relationships between length of infested shells and length of Parasyllidea humesi
Fig. 2 in The symbiotic hesionid Parasyllidea humesi Pettibone, 1961 (Annelida: Polychaeta) hosted by Scrobicularia plana (da Costa, 1778) (Mollusca: Bivalvia: Semelidade) in European waters
Fig. 2 Scrobicularia plana (Da Costa 1778). a Measurements taken on shells: length(l), width (w) and height (h). Parasyllidea humesi Pettibone 1961. b Whole body, dorsal view. c Detail of anterior end, dorsal view. Scale bar: 3 mm, b and 1 mm, c
Fig. 1 Parasyllidea humesi Pettibone 1961 in The symbiotic hesionid Parasyllidea humesi Pettibone, 1961 (Annelida: Polychaeta) hosted by Scrobicularia plana (da Costa, 1778) (Mollusca: Bivalvia: Semelidade) in European waters
Fig. 1 Parasyllidea humesi Pettibone 1961. Geographic location of the two known populations in the Republic of Congo and in the Gulf of Cádiz (Caño Sancti Petri and Río San Pedro) and location of the remaining studied estuaries: (1) Ria Formosa; (2) Guadalquivir; (3) Salado; (4) Barbate; (5) Palmones
Fig. 5 in The symbiotic hesionid Parasyllidea humesi Pettibone, 1961 (Annelida: Polychaeta) hosted by Scrobicularia plana (da Costa, 1778) (Mollusca: Bivalvia: Semelidade) in European waters
Fig. 5 Scrobicularia plana (Da Costa 1778). Relationships of length vs. width (a), height (b), and biomass (c) in infested and non-infested specimens
Fig. 2 in Revealing the diversity of the green Eulalia (Annelida, Phyllodocidae) species complex along the European coast, with description of three new species
Fig. 2 Scheme of the morphotype of Eulalia clavigera, showing the morphometric measurements used for analysis. a Anterior end. b Parapodia. Abbreviations: CLL, length of chaetigerous lobes; CLH, height of chaetigerous lobes; AL, length of antennae; PL, length of palps; MAL, length of middle antenna; DTL, length of dorsal tentac-
Fig. 6 in Revealing the diversity of the green Eulalia (Annelida, Phyllodocidae) species complex along the European coast, with description of three new species
Fig. 6 Live, relaxed specimens of Eulalia (WL: worm length). a Eulalia feliciae sp. nov., specimen DBUA0002478.01.v07, dorsal view, greenish coloration. b Eulalia madeirensis sp. nov., specimen DBUA0002479.01. v03, dorsal view, faint yellowish/light green coloration. c Eulalia xanthomucosa sp. nov., specimen from the Natural History Museum, London (left) and specimen BI-2014/15–077 (right), dorsal view, bright yellow coloration
Fig. 3 in Revealing the diversity of the green Eulalia (Annelida, Phyllodocidae) species complex along the European coast, with description of three new species
Fig. 3 Phylogenetic tree and respective COI haplotypes and MOTU locations. a Phylogenetic tree reconstructed using Bayesian inference based on concatenated COI, ITS regions and 28S sequences, with information regarding the different MOTU delineation methods. BINs were used only for COI. MOTU GB1 only have COI sequences and was not present in BOLD systems preventing BIN analysis. Only the bootstrap support over 0.85 BI and 85 ML is shown. Each different consensus MOTU is represented by the respective number, with the different colors corresponding to the respective geographic
Fig. 7 Live, relaxed specimens from E in Revealing the diversity of the green Eulalia (Annelida, Phyllodocidae) species complex along the European coast, with description of three new species
Fig. 7 Live, relaxed specimens from E. xanthomucosa sp. nov. exhibiting yellow coloration and high prevalence of yellowish mucus. a Mucus present in the posterior end of the body (specimen from David Fenwick's private collection). b Mucus present in the median part of the body (specimen from David Fenwick's private collection)
FIGURES 13–14. L in The European Lepidocyrtus Bourlet, 1839 (Collembola: Entomobryidae)
FIGURES 13–14. L. curvicollis: 13, interocular chaetotaxy (right ocular area); 14, abd. II complete chaetotaxy (left side), same simbols as in Fig. 6, arrows indicate differences with respect to Fig. 6.
Figure 4 in Dissecting copepod diversity at different spatial scales in southern European groundwater
Figure 4. (A) Mean species richness of the local units in karstic and porous aquifers in each region (standard error bars shown); (B) total species richness of karstic and porous aquifers in each region; (C) mean species richness of local units in the four habitat types in each region (standard error bars shown); (D) total species richness of the four habitat types in each region.
Figure 2 in Invasion of Eurytemora sibling species (Copepoda: Temoridae) from north America into the Baltic Sea and European Atlantic coast estuaries
Figure 2. The phylogenetic tree constructed on the basis of 52 nucleotide sequences of a region of the Eurytemora affinis cytochrome oxidase I gene (611 base pairs). The indices of bootstrap analysis (%) are shown (values below 50 are not presented) U-L, V, N - Gulf of Finland; R, Riga Bay; VL, Vistula Lagoon. The sites of sample collection are shown in Figure 1. Eurytemora herdmani and Eurytemora pacifica were used as an outgroup.
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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.