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Fig. 3 in Diversification Pattern of the Widespread Holarctic Cuckoo Bumble Bee, Bombus flavidus (Hymenoptera: Apidae): The East Side Story
Fig. 3. Bayesian general mixed Yule-coalescent model (bGMYC) results based on COI phylogenetic tree. The colored matrix corresponds to the pairwise probabilities of conspecificity (color scale below the figure).
Fig. 2 in Diversification Pattern of the Widespread Holarctic Cuckoo Bumble Bee, Bombus flavidus (Hymenoptera: Apidae): The East Side Story
Fig. 2. Relationships of Bombus flavidus lineages inferred with cytochrome oxidase I (COI). (A) Haplotype network for the sequenced individuals, highlighting the connections between the haplotypes shown on the map (right). (B) Bayesian tree of B. flavidus and related species. Clade support values are Bayesian posterior probabilities.The right zoomed-in part of the figure highlights population structure. (C) Visualization of the major haplotypes mapped at their respective geographical locations.
Fig. 5 in Diversification Pattern of the Widespread Holarctic Cuckoo Bumble Bee, Bombus flavidus (Hymenoptera: Apidae): The East Side Story
Fig. 5. Dendrogram based on cephalic labial gland secretions of Bombus flavidus with represented Eastern Nearctic (purple) and Palearctic + western Nearctic (green) lineages. This cluster was obtained by hierarchical clustering using an unweighted pair-group method with arithmetic mean (UPGMA) based on correlation distance matrices calculated from the relative abundance of the compounds present in cephalic labial gland secretions (CLGS).The values near nodes represent multiscale bootstrap resampling values. Multiple response permutation procedure (MRPP) indicates level of CLGS differentiation between taxa.
Fig. 1 in Diversification Pattern of the Widespread Holarctic Cuckoo Bumble Bee, Bombus flavidus (Hymenoptera: Apidae): The East Side Story
Fig. 1. Global distribution of Bombus flavidus (Palearctic) and Bombus fernaldae (Nearctic). Distributional ranges are approximated based on literature records (Williams et al. 2014; Ascher and Pickering 2020) and thus are not meant to be accurate at a fine scale.
Fig. 9 in Diversification Pattern of the Widespread Holarctic Cuckoo Bumble Bee, Bombus flavidus (Hymenoptera: Apidae): The East Side Story
Fig. 9. Geographic distribution of B. flavidus color patterns in Oregon. (A) Average percent of individual yellow pile; (B) boxplots comparing total body pile percent yellow between individuals from Western and Eastern localities.The asterisks indicate a significant different between boxplots (unpaired two-tailed t-test, ***P <0.0001).
Fig. 4 in Diversification Pattern of the Widespread Holarctic Cuckoo Bumble Bee, Bombus flavidus (Hymenoptera: Apidae): The East Side Story
Fig. 4. Median-joining network of haplotypes based on nuclear genes ITS and PEPCK. Circle sizes are proportional to frequencies of haplotypes. Colors of haplotypes refer to geographic areas (Fig. 3). Black bars on lines represent the number of mutation(s) between two close haplotypes. Black circles are outgroups (B. skorikovi and B. norvegicus).
Fig. 6 in Diversification Pattern of the Widespread Holarctic Cuckoo Bumble Bee, Bombus flavidus (Hymenoptera: Apidae): The East Side Story
Fig. 6. (A) Ordination of individuals of Bombus flavidus along the first two principal components (PCA1 and PCA2) of the principal components analysis of the landmark configuration variability. (B) Ordination of individuals of Bombus flavidus along the two first axes (LDA1 and LDA2) of the linear discriminant analysis of the landmark configuration variability.
Fig. 8 in Diversification Pattern of the Widespread Holarctic Cuckoo Bumble Bee, Bombus flavidus (Hymenoptera: Apidae): The East Side Story
Fig. 8. Global distribution of color patterns of Bombus flavidus. The extremes and intermediates of color observed are shown for each region. Color patterns with asterisks (Scandinavia) were extracted from LØken (1985).
Fig. 1 in Widespread support for a global species list with a formal governance system
Fig. 1. Survey results showing (A) generally strong agreement that there would be a net benefit to creation of a single global species list across all respondent groups; (B) overall preferences for representation on an oversight board; (C) overall preferences for oversight options of an independent board, a committee of an existing organization, or an NGO; and (D) common problems encountered by respondents, including competing lists, outdated information, and the absence of lists.
Figure 8 in Modern hydrophilid clades present and widespread in the Late Jurassic and Early Cretaceous (Coleoptera: Hydrophiloidea: Hydrophilidae)
Figure 8. Reconstructions of the clypeus shape and meso- and metathoracic morphology of the Early Cretaceous hydrophilid genera known in adult stage (three-dimensional structure of the mesoventrite not reconstructed). Alegorius gen. nov. (A, B); Cretoxenus gen. nov. (C, D); Hydroyixia gen. nov. (E, F). Head and thorax of the respective genus not to scale.
Figure 7 in Modern hydrophilid clades present and widespread in the Late Jurassic and Early Cretaceous (Coleoptera: Hydrophiloidea: Hydrophilidae)
Figure 7. Hydrophilid fossils from Early Cretaceous Yixian Formation, China. Alegorius yixianus sp. nov.: holotype CNU 2009079, whole specimen (A), detail of meso- and metaventrite (B), detail of abdominal apex (C); paratype CNU 2009078, whole specimen (D), detail of mesoventrite (E). Hydroyixia elongata sp. nov.: paratype CNU 2009075, detail of head and pronotum (F), whole specimen (G); holotype CNU 2010005: whole beetle, piece and counterpiece (H, I), detail of head (J), detail of meso- and metaventrite (K), detail of abdominal apex (L). Hydroyixia latissima sp. nov.: holotype CNU 2009074, detail of abdominal apex (M), whole specimen in dry condition (N) and under alcohol (O). Abbreviations: apls, anapleural suture; abem, apical emargination of abdominal ventrite 5.
Figure 9 in Modern hydrophilid clades present and widespread in the Late Jurassic and Early Cretaceous (Coleoptera: Hydrophiloidea: Hydrophilidae)
Figure 9. Known distribution of the Hydrophilidae in the Late Jurassic and Early Cretaceous. 1, Solnhofen, Germany; 2, Talbragar, Australia; 3, Baissa, Russia; 4, Yixian Formation, China; 5, Koonwarra, Australia.
Figure 4 in Modern hydrophilid clades present and widespread in the Late Jurassic and Early Cretaceous (Coleoptera: Hydrophiloidea: Hydrophilidae)
Figure 4. Results of the phylogenetic analyses of the position of Baissalarva hydrobioides. Unconstrained analysis, strict consensus of seven most-parsimonious trees of 207 steps (A); single most parsimonious tree of length 240 steps resulting from the constrained analysis (B).
Figure 6 in Modern hydrophilid clades present and widespread in the Late Jurassic and Early Cretaceous (Coleoptera: Hydrophiloidea: Hydrophilidae)
Figure 6. Fossil and recent representatives of the Hydrobiusini and Hydrophilini. Baissalarva hydrobioides sp. nov.: holotype PIN 3063/6975, anterior part of the piece (A), detail of the head of the piece (B), detail of the head of the counterpiece (C); paratype PIN 3063/6977 (D). Larva of extant Limnoxenus niger (Hydrobiusini): whole larva in dorsal view (E), detail of head (G). Larva of extant Sternolophus rufipes (Hydrophilini): whole larva in dorsal view (F), detail of head (H). Holotype of Cretoxenus australis sp. nov. NMVP 103312, piece and counterpiece (I, J). Extant hydrobiusine Limnoxenus zealandicus in ventral view, whole beetle (K) and detail of meso- and metaventrite (L). Abbreviations: md, mandible; mtvpr, metaventral process.
Figure 3 in Modern hydrophilid clades present and widespread in the Late Jurassic and Early Cretaceous (Coleoptera: Hydrophiloidea: Hydrophilidae)
Figure 3. Early Cretaceous representatives of the Hydrobiusini. Cretoxenus australis gen. nov., sp. nov., Koonwarra, Australia, NMVP 103312, piece and counterpiece (A, B). Baissalarva hydrobioides gen. nov., sp. nov. from Baissa, Russia: paratype PIN 3063/6977 (C); holotype PIN 3063/6975: piece, detail of the head (D), counterpiece, detail of the head (E), whole specimen, counterpiece (F). Abbreviations: absc, abdominal dorsal sclerite; absc4, absc7, abdominal dorsal sclerite of segment 4 or 7; aes3, metanepisternum; apls, anapleural suture; cersc, cervical sclerite; dpl8, dorsal plate on abdominal segment 8; epl, epistomal lobe; md, mandible; men, mentum; mssc, mesoscutum; mstr1, mesotarsomere 1; msv, mesoventrite; mxp, maxillary palpus; mtsc, metascutum; ns, nasale; occf, occipital foramen; pros, prosternum; sbm, submentum; scsh, scutellar shield; sstr, sutural stria; ttr, tracheal trunk.
Figure 2 in Modern hydrophilid clades present and widespread in the Late Jurassic and Early Cretaceous (Coleoptera: Hydrophiloidea: Hydrophilidae)
Figure 2. Alegorius yixianus gen. nov., sp. nov. from the Yixian Formation, China. Holotype, CNU 2009079 (A); paratype, CNU 2009078 (B). Abbreviations: abem, apical emargination of abdominal ventrite 5; aes3, metanepisternum; bst, maxillary basistipes; fmtta, free metatibial anterobasal angle; lb, labrum; men, mentum; mstr1, mesotarsomere 1; msv, mesoventrite; pros, prosternum; sstr, sutural stria; tf, transverse fold of prothorax.
Figure 1 in Modern hydrophilid clades present and widespread in the Late Jurassic and Early Cretaceous (Coleoptera: Hydrophiloidea: Hydrophilidae)
Figure 1. Late Jurassic fossils of the Hydrophilidae. Protochares brevipalpis gen. nov., sp. nov., AMF109568, Talbragar, Australia (A, B, F); 'Mesosperchus' schultzi Ponomarenko, 1985, NHMW 1985/20, Solnhofen, Germany: whole specimen (C, G–H), details of the head of the piece using different lighting (D–E). Abbreviations: aes3, metanepisternum; fcs, frontoclypeal suture; gs, gular suture; mttr1, metatarsomere 1; mxp, maxillary palpus; prospr, prosternal process; scstr, scutellar stria; sstr, sutural stria.
Supplementary material 1 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Supplementary material 1 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Supplementary material 2 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Supplementary material 2 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Additional material for the article "Widespread fracture movements during a volcano-tectonic unrest: the Reykjanes Peninsula, Iceland, from 2019–2021 TerraSAR-X interferometry"
<p><span>Additional Material for the article "Widespread fracture movements during a volcano-tectonic unrest: the Reykjanes Peninsula, Iceland, from 2019–2021 TerraSAR-X interferometry" published in Bulletin of Volcanology (<a href="https://doi.org/10.1007/s00445-023-01699-0" target="_blank" rel="noopener">https://doi.org/10.1007/s00445-023-01699-0</a>).<br></span></p> <p> </p> <p><span>Description of the content in the zip folder:</span></p> <p><span>The georeferenced mapped discontinuities are listed in text files that are classed </span><span>by interferogram date and track. Each file contains a list of longitude and lati</span><span>tude values of the mapped fractures, with the beginning of each fracture trace</span><span> </span><span>annotated by a line starting with ">" and the fracture ID (i.e., the number of </span><span>the fracture starting at 1 in each file), the QI (1, 2 or 3), the estimated sense of</span><span> </span><span>motion (N for normal or SL for strike-slip), and the indicative LOS amplitude</span><span> </span><span>of motion.</span></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.