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562 results for “genetic divergences”
Figure 26 in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 26. Distribution of A, Pseudoanthidium kaspareki; B, P. rozeni.
Figure 15. Neotype Anthidium stigmaticorne. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 15. Neotype Anthidium stigmaticorne. A, dorsal view; B, labels; C, face; D, lateral view.
Figure 14. Lectotype Anthidium frontale. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 14. Lectotype Anthidium frontale. A, dorsal view; B, face; C, labels; D, lateral view.
Figure 5. Lectotype, Pseudoanthidium nanum. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 5. Lectotype, Pseudoanthidium nanum. A, lateral view; B, dorsal view; C, labels.
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 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 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 7. Caparinia ictonyctis Lawrence, 1955, tritonymph. A in Validation of the status of a species with high CO1 and low nuclear genetic divergences: the scab mite Caparinia ictonyctis stat. res. (Acariformes: Psoroptidae) parasitizing the African hedgehog Atelerix albiventris
FIGURE 7. Caparinia ictonyctis Lawrence, 1955, tritonymph. A—dorsal view; B—ventral view.
FIGURE 9. Caparinia ictonyctis Lawrence, 1955, male. A in Validation of the status of a species with high CO1 and low nuclear genetic divergences: the scab mite Caparinia ictonyctis stat. res. (Acariformes: Psoroptidae) parasitizing the African hedgehog Atelerix albiventris
FIGURE 9. Caparinia ictonyctis Lawrence, 1955, male. A—dorsal view; B—ventral view.
FIGURE 6 in A new species of Uroplatus (Gekkonidae) from Ankarana National Park Madagascar, of remarkably high genetic divergence
FIGURE 6. Preserved holotype of Uroplatus fetsy sp. nov. (ZSM 288/2004, field number FGZC 552).
Figure 3 from: Colihueque N, Gantz A, Rau JR, Parraguez M (2015) Genetic divergence analysis of the Common Barn Owl Tyto alba (Scopoli, 1769) and the Short-eared Owl Asio flammeus (Pontoppidan, 1763) from southern Chile using COI sequence. ZooKeys 534: 135-146. https://doi.org/10.3897/zookeys.534.5953
Figure 3 - Unrooted haplotype network of COI gene sequence, based on a median-joining network for the Common Barn Owl and the Short-eared Owl. The area of each circle is proportional to the number of individuals containing the haplotype. Open circles indicate mutational events and numbers refer to the variable nucleotide positions. A Common Barn Owl; Solid black: Chile/South America; white with cross lines: Argentina/South America; white with forward diagonal lines: USA/ North America; white with horizontal lines: El Salvador/ Central America; white with vertical lines: Canada/ North America; white with backward diagonal lines: Sweden/ northern Europe; white with backward diagonal cross lines: Australia/ Australasia. B Short-eared Owl; Solid black: Chile/South America; white with cross lines: Argentina/South America; white with forward diagonal lines: USA/ North America; white with horizontal lines: Canada/ North America; white with backward diagonal lines: Sweden/ northern Europe; white with horizontal lines: Russia/ northern Asia; white with cross diagonal lines: Norway/ northern Europe.
Figure 2 from: Colihueque N, Gantz A, Rau JR, Parraguez M (2015) Genetic divergence analysis of the Common Barn Owl Tyto alba (Scopoli, 1769) and the Short-eared Owl Asio flammeus (Pontoppidan, 1763) from southern Chile using COI sequence. ZooKeys 534: 135-146. https://doi.org/10.3897/zookeys.534.5953
Figure 2 - Haplotype designation, variable nucleotide positions of COI gene sequence analysis, with the haplotype frequency observed in each locality. A Haplotypes of Common Barn Owls (n = 21) B haplotypes of Short-eared Owl (n = 10). Number refers to positions identified in the alignment. For all haplotypes, variable nucleotides are indicated while identity is indicated by slashes.
Figure 4 from: Colihueque N, Gantz A, Rau JR, Parraguez M (2015) Genetic divergence analysis of the Common Barn Owl Tyto alba (Scopoli, 1769) and the Short-eared Owl Asio flammeus (Pontoppidan, 1763) from southern Chile using COI sequence. ZooKeys 534: 135-146. https://doi.org/10.3897/zookeys.534.5953
Figure 4 - Phylogenetic estimate of relationships among specimens of the Common Barn Owl from different locations based on analysis of 582 bp of the mitochondrial cytochrome c oxidase subunit I gene (COI). The haplotype, locality and Genbank accession number (in parentheses) for each specimen are shown. The branch lengths are drawn proportional to the relative amount of volutionary change. Scale indicates the sequence divergence estimated from the number of nucleotide substitutions per site A Maximum likelihood tree with the bootstrap support (%) indicated for each node B Bayesian tree with the posterior probability values indicated for each node.
Figure 1 from: Colihueque N, Gantz A, Rau JR, Parraguez M (2015) Genetic divergence analysis of the Common Barn Owl Tyto alba (Scopoli, 1769) and the Short-eared Owl Asio flammeus (Pontoppidan, 1763) from southern Chile using COI sequence. ZooKeys 534: 135-146. https://doi.org/10.3897/zookeys.534.5953
Figure 1 - Map of southern Chile, illustrating the collection places of Common Barn Owl and Short-eared Owl specimens. Black squares- Common Barn Owl (n = 9), white square- Short-eared Owl (n = 1).
Figure 3 from: Sitnikova T, Kovalenkova M, Peretolchina T, Sherbakov D (2016) A new, genetically divergent species of Pseudobaikalia Lindholm, 1909 (Caenogastropoda, Baicaliidae). ZooKeys 593: 1-14. https://doi.org/10.3897/zookeys.593.8511
Figure 3 - Scanning electron micrographs of Pseudobaikalia michelae sp. n. A, B Operculum, dorsal view to left and ventral view to right C, E Protoconch D Penis, dorsal view. Scale bars: 0.5 mm (A, B); 0.1 mm (C, D, E).
Figure 5 from: Sitnikova T, Kovalenkova M, Peretolchina T, Sherbakov D (2016) A new, genetically divergent species of Pseudobaikalia Lindholm, 1909 (Caenogastropoda, Baicaliidae). ZooKeys 593: 1-14. https://doi.org/10.3897/zookeys.593.8511
Figure 5 - Genitalia of Pseudobaikalia michelae sp. n. A, C Ventral and dorsal view of female genitalia B Section of capsule gland and ventral channel D Penis. Abbreviations: ag—albumen gland; cg—capsule gland; cov—coil oviduct; go—genitalia opening; vch—ventral channel; vd—vas deference. Scale bars 0.5 mm.
Figure 4 from: Sitnikova T, Kovalenkova M, Peretolchina T, Sherbakov D (2016) A new, genetically divergent species of Pseudobaikalia Lindholm, 1909 (Caenogastropoda, Baicaliidae). ZooKeys 593: 1-14. https://doi.org/10.3897/zookeys.593.8511
Figure 4 - Radular teeth of Pseudobaikalia michelae sp. n. Scale bars: 10 μm (A, B, C); 30 μm (D, E).
Figure 2 from: Sitnikova T, Kovalenkova M, Peretolchina T, Sherbakov D (2016) A new, genetically divergent species of Pseudobaikalia Lindholm, 1909 (Caenogastropoda, Baicaliidae). ZooKeys 593: 1-14. https://doi.org/10.3897/zookeys.593.8511
Figure 2 - Shells of the type specimens of Pseudobaikalia michelae sp. n. and syntypes of other species of Pseudobaikalia genus from ZIN collection. A Holotype Pseudobaikalia michelae sp. n. B Paratypes Pseudobaikalia michelae sp. n. used for analyses C Pseudobaikalia michelae sp. n. (=Leucosia angarensis var. pulla, det. Dybowski, No. 1) D Pseudobaikalia elegantula (No. 2) E Pseudobaikalia jentteriana (No. 1) F Pseudobaikalia pulla pulla (No. 1) G Pseudobaikalia pulla tenuicosta (No.1) H Pseudobaikalia zachwatkini (No. 1) I Parabaikalia elata (=Baikalia angarensis elata, No.1) J Pseudobaikalia cancellata (No. 1) K Pseudobaikalia contabulata (No. 1). Scale bar 1 mm.
Figure 1 from: Sitnikova T, Kovalenkova M, Peretolchina T, Sherbakov D (2016) A new, genetically divergent species of Pseudobaikalia Lindholm, 1909 (Caenogastropoda, Baicaliidae). ZooKeys 593: 1-14. https://doi.org/10.3897/zookeys.593.8511
Figure 1 - The location of Pseudobaikalia michelae sp. n. sampling sites in Lake Baikal. Site numbers correspond to 1 Kultuk Bay 2 near Utulik settlement 3 Murinskaya Bank 4 Barguzin Bay.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.