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Figure 5 from: Muhammad F, Lü Z-m, Liu L, Gong L, Du X, Shafi M, Kaleri HA (2018) Genetic structure of Octopus minor around Chinese waters as indicated by nuclear DNA variations (Mollusca, Cephalopoda). ZooKeys 775: 1-14. https://doi.org/10.3897/zookeys.775.24258
Figure 5 Median-joining networking drawn based on ODH gene haplotypes. Colours represent the corresponding population frequencies. Key: Dalian; Dongshan; Nantong; Qingdao; Shanghai; Wenzhou; Xiamen; Zhoushan.
Figure 2 from: Muhammad F, Lü Z-m, Liu L, Gong L, Du X, Shafi M, Kaleri HA (2018) Genetic structure of Octopus minor around Chinese waters as indicated by nuclear DNA variations (Mollusca, Cephalopoda). ZooKeys 775: 1-14. https://doi.org/10.3897/zookeys.775.24258
Figure 2 Neighbour-joining phylogenetic tree constructed based on RD gene sequences. Key: DL = Dalian, N = Nantong, Q = Qingdao, S = Shanghai, W = Wenzhou, X = Xiamen, Z = Zhoushan.
Figure 4 from: Muhammad F, Lü Z-m, Liu L, Gong L, Du X, Shafi M, Kaleri HA (2018) Genetic structure of Octopus minor around Chinese waters as indicated by nuclear DNA variations (Mollusca, Cephalopoda). ZooKeys 775: 1-14. https://doi.org/10.3897/zookeys.775.24258
Figure 4 Median-joining networking drawn based on RD gene haplotypes. Colours represent the corresponding population frequencies. Key: Dalian; Dongshan; Nantong; Qingdao; Shanghai; Wenzhou; Xiamen; Zhoushan.
Figure 3 from: Muhammad F, Lü Z-m, Liu L, Gong L, Du X, Shafi M, Kaleri HA (2018) Genetic structure of Octopus minor around Chinese waters as indicated by nuclear DNA variations (Mollusca, Cephalopoda). ZooKeys 775: 1-14. https://doi.org/10.3897/zookeys.775.24258
Figure 3 Neighbour-joining tree constructed based on the ODH gene. Key: DL = Dalian, N = Nantong, Q = Qingdao, S = Shanghai, W = Wenzhou, X = Xiamen, Z = Zhoushan.
Figure 3 from: Rocha-Méndez A, Sánchez-González LA, Arbeláez-Cortés E, Navarro-Sigüenza AG (2018) Phylogeography indicates incomplete genetic divergence among phenotypically differentiated montane forest populations of Atlapetes albinucha (Aves, Passerellidae). ZooKeys 809: 125-148. https://doi.org/10.3897/zookeys.809.28743
Figure 3 Bayesian skyline plot derived from the concatenated gene dataset of Atlapetesalbinucha species. Time in millions of years. Population size change (Ne*generation time) in the Y axis. Mean estimate is shown as a thick solid line, and the 95% HDP limits are shown in solid purple color area surrounding the mean estimate.
Figure 3 from: Decker P (2018) Phylogenetic and morphological discord indicates introgressive hybridisation in two genera of Australian millipedes (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 809: 1-14. https://doi.org/10.3897/zookeys.809.30087
Figure 3 Bootstrap consensus tree for the combined mt COI+16S dataset in Pogonosternum; maximum likelihood, 1000 bootstrap replicates. Coloured dotted lines indicate specimens with similar gonopod morphology. Coloured bars indicate last male leg pairs with tibial and tarsal brushes (leg pair 7 = blue, leg pair 9 = green).
Figure 4 from: Rocha-Méndez A, Sánchez-González LA, Arbeláez-Cortés E, Navarro-Sigüenza AG (2018) Phylogeography indicates incomplete genetic divergence among phenotypically differentiated montane forest populations of Atlapetes albinucha (Aves, Passerellidae). ZooKeys 809: 125-148. https://doi.org/10.3897/zookeys.809.28743
Figure 4 Maxent ENMs for A.albinucha species projected into present and past scenarios. Darker blue areas depict higher logistic prediction values. ENM projected in the a present b the Mid-Holocene Climatic Optimum (MH) c the Last Glacial Maximum (LGM) and d the Last Interglacial (LIG).
Figure 1 from: Rocha-Méndez A, Sánchez-González LA, Arbeláez-Cortés E, Navarro-Sigüenza AG (2018) Phylogeography indicates incomplete genetic divergence among phenotypically differentiated montane forest populations of Atlapetes albinucha (Aves, Passerellidae). ZooKeys 809: 125-148. https://doi.org/10.3897/zookeys.809.28743
Figure 1 Atlapetesalbinucha distribution shown in green stapled lines, based on Sánchez-González et al. (2015) and Natureserve (http://natureserve.org). Blue dots depict tissue samples used in the present study. Red dots depict records of the species used to construct the distribution model. Bird pictures depict the geographic regions where color morphs are found. Blue line depicts the location of the putative distribution barrier of the morphs in Chiapas.
Figure 6 from: Decker P (2018) Phylogenetic and morphological discord indicates introgressive hybridisation in two genera of Australian millipedes (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 809: 1-14. https://doi.org/10.3897/zookeys.809.30087
Figure 6 Map of South Australia and southern Mt Lofty Ranges showing localities for Somethus species: S.castaneus (filled triangle), S.inflatus (open triangle), S.lancearius (square), and S.castaneus from Mt. Osmond (yellow star).
Figure 2 from: Rocha-Méndez A, Sánchez-González LA, Arbeláez-Cortés E, Navarro-Sigüenza AG (2018) Phylogeography indicates incomplete genetic divergence among phenotypically differentiated montane forest populations of Atlapetes albinucha (Aves, Passerellidae). ZooKeys 809: 125-148. https://doi.org/10.3897/zookeys.809.28743
Figure 2 A Dated Bayesian maximum clade credibility tree showing phylogenetic relationships among members of Atlapetesalbinucha species. Node bars depict 95% HDP interval, scale bar represents millions of years. Nodal values above branches indicate posterior probabilities/ bootstrap supports of BI/ML. Capital letters depict haplotypes. An asterisk (*) indicate birds representing yellow morphs B Median-joining haplotype network for the concatenated dataset. Each color depicts the geographic provenance of samples: green-northern Chiapas (subspecies albinucha), red-southern Chiapas (subspeciesgriseipectus), blue-El Salvador (subspecies griseipectus), yellow-Honduras (subspecies fuscipygius) and light blue-Colombia (subspecies gutturalis). Each branch represents a single nucleotide change, transversal black lines along branches depict the occurrence of three mutations. Gray dots indicate median vectors inferred for the data.
Figure 2 from: Decker P (2018) Phylogenetic and morphological discord indicates introgressive hybridisation in two genera of Australian millipedes (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 809: 1-14. https://doi.org/10.3897/zookeys.809.30087
Figure 2 Pogonosternumnigrovirgatum (Carl, 1902), ♂, right gonopod. A, B AMS KS96017 Ferntree Gully C, DNMV K-10248 from Sandringham and Brighton. Pogonosternumjeekeli Decker, sp. n., ♂, right gonopod E, FNMV K-10252 from Dyer Creek G, HNMV K-10250 from Bemm River. A, C Posterior view B, D Mesal view. Scale bar: 0.5 mm.
Figure 1 from: Decker P (2018) Phylogenetic and morphological discord indicates introgressive hybridisation in two genera of Australian millipedes (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 809: 1-14. https://doi.org/10.3897/zookeys.809.30087
Figure 1 Pogonosternumcf.nigrovirgatum "Dargo", male, right gonopod (NMV K-12202). A Posterior view B Lateral view C Anterior view D Mesal view. Abbreviations: fp1 = femoral process 1; fp2 = femoral process 2; lp = lateral process; prof = prolongation of femorite; S = solenomere; F = femorite. Scale bar: 0.5 mm.
Figure 5 from: Decker P (2018) Phylogenetic and morphological discord indicates introgressive hybridisation in two genera of Australian millipedes (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 809: 1-14. https://doi.org/10.3897/zookeys.809.30087
Figure 5 COI and 28S bootstrap consensus trees for Somethus species; maximum likelihood, 1000 bootstrap replicates.
Figure 4 from: Decker P (2018) Phylogenetic and morphological discord indicates introgressive hybridisation in two genera of Australian millipedes (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 809: 1-14. https://doi.org/10.3897/zookeys.809.30087
Figure 4 Distribution map of Pogonosternumnigrovirgatum (red circles), P.jeekeli (orange diamonds) and P.cf.nigrovirgatum "Dargo" (yellow star) in southeastern Australia. Abbreviation: ACT = Australian Capital Territory.
Measuring output and impact of scientific journals in dentistry and oral medicine using bibliometric indices
<p>Dataset for all analyses done in the study</p>
Supplementary material 1 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
: Data type: statistical data
Supplementary material 2 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
: Data type: statistical data
Supplementary material 3 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
: Data type: phylogenetic data
Figure 5 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
Figure 5 Biogeographic and phylogenetic expectations for a 'vicariance by erosion' scenario as hypothesized for the southern Cumberland Plateau. A–C Karst (gray) erodes and fragments over time, leading to the isolation and divergence of cave populations (colored circles) in the remaining patches of karst D A phylogeny consistent with the vicariance by erosion process, with taxa that diverge early distributed at the periphery of the eroding region.
Figure 3 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
Figure 3 Ultrametric tree for the hirtus-group. Bayesian tree estimated from combined partial mitochondrial sequence data. Branches supported by posterior probability >0.90 are labeled with values or, for branches with posterior probability of 1.0, an asterisk. Blue bars indicate 95% confidence intervals of estimated ages for the nodes. Taxa are labeled with species name and specimen identifier (Table 1). Scale at bottom indicates divergence times in millions of years as estimated by BEAST (Drummond et al. 2012). Branch colors correspond to those in Figure 2A.
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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.