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Data set for: Crustal Azimuthal Anisotropy Beneath the Southeastern Tibetan Plateau and its Geodynamic Implications
<p>Abstract of the original paper:</p> <p>Zheng, T., Ding, Z., Ning, J., Chang, L., Wang, X., Kong, F., Liu, K.H., & Gao, S.S. (2018).<br> Crustal azimuthal anisotropy beneath the southeastern Tibetan Plateau and its geodynamic implications.<br> <em><strong>Journal of Geophysical Research: Solid Earth, 123(11)</strong>, 9733-9749. </em> <a href="https://agupubs.onlinelibrary.wiley.com/doi/abs/10.1029/2018JB015995"> https://doi.org/10.1029/2018JB015995</a></p> <p>The fast orientation and magnitude of crustal azimuthal anisotropy beneath the southeastern Tibetan Plateau and adjacent areas are measured by analyzing the sinusoidal moveout of the <em>P</em> to <em>S</em> converted phase from the Moho. Beneath the tectonically active plateau, the mean magnitude is 0.48 ± 0.13 s, which is about twice as large as that observed in the stable Sichuan Basin (0.23 ± 0.10 s). The two areas are separated by the Longmenshan fault zone, a zone of devastating earthquakes including the 12 May 2008 <em>M</em><sub><em>W</em></sub> 7.9 Wenchuan earthquake. Fault orthogonal fast orientations observed in the southern Longmenshan fault zone, where previous studies have revealed high crustal <em>V</em><sub><em>p</em></sub>/<em>V</em><sub><em>s</em></sub> and suggested the presence of mid‐lower crustal flow, may reflect flow‐induced lattice preferred orientation of anisotropic minerals. Fault parallel anisotropy in the central segment of the fault zone is most likely related to fluid filled fractures, and fault perpendicular extensional cracks are probably responsible for the observed anisotropy in the northern segment. The crustal anisotropy measurements, when combined with results from previous studies, suggest the existence of mid‐lower crustal flow beneath the southeastern margin of the plateau. Comparison of crustal anisotropy obtained before and after the Wenchuan earthquake suggests that the earthquake has limited influence on whole crustal anisotropy, although temporal changes of anisotropy associated with the earthquake have been reported using splitting of shear waves from local earthquakes occurred in the upper crust.</p>
FIGURE 2. 50 in A molecular phylogeny of the genus Psittacula sensu lato (Aves: Psittaciformes: Psittacidae: Psittacula, Psittinus, Tanygnathus, † Mascarinus) with taxonomic implications
FIGURE 2. 50% majority-rule consensus tree of the Bayesian inference of relationships among representatives of Psittacula s.l. (Psittacula, Tanygnathus, Psittinus) based on Bayesian analysis (BEAST) of the concatenated data set (CYTB, RAG-1); maximum clade credibility tree, HKY model. Bayesian posterior probabilities above 0.85 are indicated left of the slash. Maximum likelihood methods (RAxML) gave an identical tree topology, bootstrap values (ML) above 70 are indicated after the slash.
FIGURE 1 in A molecular phylogeny of the genus Psittacula sensu lato (Aves: Psittaciformes: Psittacidae: Psittacula, Psittinus, Tanygnathus, † Mascarinus) with taxonomic implications
FIGURE 1. Schematic illustration of all species plus some additional subspecies of the Psittacula s.l. group (including Psittinus, Tanygnathus, and †Mascarinus). Extinct taxa are indicated with a '†'. Only males are shown. Taxa which were sampled for our phylogenetic reconstruction are indicated with an asterisk (*). Lines highlight distinctive characters.
FIGURE 3 in A molecular phylogeny of the genus Psittacula sensu lato (Aves: Psittaciformes: Psittacidae: Psittacula, Psittinus, Tanygnathus, † Mascarinus) with taxonomic implications
FIGURE 3. Recommended taxonomic revision of the Psittacula s.l. group. Schematic illustration of all species plus additional subspecies for our study of the Psittacula s.l. group (including Psittinus, Tanygnathus, and †Mascarinus). Morphological and genetic clades are separated by dotted lines (see FIGURE 1 for conventions).
FIGURE 5 in Taxonomic and systematic implications of the revision of the phylogenetic relations in the genus Ectinogonia Spinola 1837 (Coleoptera: Buprestidae) of Central Chile
FIGURE 5. Haplotype network of Wg fragment from Ectinogonia species studied. Each color represents a species. Circle size indicates the frequency of the haplotype. Mutational steps between haplotypes are indicated by dot marks on the axis that unites haplotypes.
FIGURE 3 in Taxonomic and systematic implications of the revision of the phylogenetic relations in the genus Ectinogonia Spinola 1837 (Coleoptera: Buprestidae) of Central Chile
FIGURE 3. Haplotype network of COI fragment from Ectinogonia species studied. Each color represents a species. Circle size indicates the frequency of the haplotype. Mutational steps between haplotypes are indicated by hash marks on the axis that unites haplotypes.
FIGURE 2 in Taxonomic and systematic implications of the revision of the phylogenetic relations in the genus Ectinogonia Spinola 1837 (Coleoptera: Buprestidae) of Central Chile
FIGURE 2. Location of the study área (A) and sampling localities (B); La Parva-Potrero Grande (1), La Obra (2), Lo Valdez- El Morado (3), Altos de Cantillana (4), Valle las Leñas (5), Volcán Descabezado Grande (6), Los Sauces (7), Las Comadres-Las Trancas (8). For each locality, numbered from 1 to 8, is the relative frequency of sampled species (circular graph) to show sympatric species.
FIGURE 4 in Rediscovery of Micryletta inornata (Boulenger, 1890) from Sumatra: redescription, molecular identity, and taxonomic implications
FIGURE 4. Micryletta inornata, syntype (male, NHM 1889.11.12.30) and topotype (male, MZB Amph 27242). A–E. Syntype, in preservation: A. dorsal view; B. ventral view; C. lateral view of head; D. ventral view of hand; E. ventral view of foot. F–J. Topotype, in preservation: F. dorsal view; G. ventral view; H. lateral view of head; I. ventral view of hand; J. ventral view of foot. Scale bars = 5 mm.
FIGURE 3 in Rediscovery of Micryletta inornata (Boulenger, 1890) from Sumatra: redescription, molecular identity, and taxonomic implications
FIGURE 3. Micryletta inornata from Sumatra in life. A–B. Adult male (MZB Amph 27242 from Aceh): A. dorsolateral view; B. ventral view. C–D. Sub-adult (MZB Amph 23570 from Deli Serdang): C. dorsolateral view; D. ventral view.
FIGURE 2. Maximum Likelihood tree for 19 in Rediscovery of Micryletta inornata (Boulenger, 1890) from Sumatra: redescription, molecular identity, and taxonomic implications
FIGURE 2. Maximum Likelihood tree for 19 samples of the genus Micryletta based on ~435 bp fragment of the mitochondrial 16S rRNA gene. Values at the branches indicate Maximum Likelihood Bootstrap Support (MLBS) and Bayesian Posterior Probabilities (BPP), respectively.
FIGURE 1 in Rediscovery of Micryletta inornata (Boulenger, 1890) from Sumatra: redescription, molecular identity, and taxonomic implications
FIGURE 1. The revised distribution of Micryletta inornata based on new locality records from Sumatra. Genetically and morphologically studied M. inornata samples (red); an additional morphologically studied M. inornata sample (green); and previously misidentified M. 'inornata' populations used for the molecular study (blue). The locality numbers are referenced in Table 1.
FIGURES 13–16 in A new species of Medinodexia Townsend (Diptera: Tachinidae) from Japan, with a discussion on phylogenetic implications of the female postabdomen in Blondeliini
FIGURES 13–16. Male postabdomen of Medinodexia fulviventris Townsend (Sabah, Malaysia, ITBC). 13. Epandrium, cercus and surstylus in lateral view. 14. Epandrium, cerci and surstyli in dorsal view (setae omitted on left side). 15. Fifth abdominal sternite in ventral view (setae omitted on left side). 16. Hypandrium, pregonite, postgonite and phallus in lateral view. Scale bars = 0.1 mm.
FIGURES 2–8 in A new species of Medinodexia Townsend (Diptera: Tachinidae) from Japan, with a discussion on phylogenetic implications of the female postabdomen in Blondeliini
FIGURES 2–8. Medinodexia japonica sp. nov. and its host. 2–7. Medinodexia japonica sp. nov. 8. Aulacophora nigripennis Motschulsky, host from which a larva of M. japonica emerged. 2–3. Male paratype (Kyushu University Ito Campus, Fukuoka Prefecture, BLKU). 2. Habitus in lateral view. 3. Habitus in dorsal view. 4. Puparium. 5–7. Female paratype (Kyushu, Fukuoka, BLKU). 5. Habitus in lateral view. 6. Habitus in dorsal view. 7. Habitus in ventral view. Scale bar = 5 mm.
FIGURES 9–12 in A new species of Medinodexia Townsend (Diptera: Tachinidae) from Japan, with a discussion on phylogenetic implications of the female postabdomen in Blondeliini
FIGURES 9–12. Male postabdomen of Medinodexia japonica sp. nov. (paratype, Kukino, Kumamoto Prefecture, BLKU). 9. Epandrium, cercus and surstylus in lateral view. 10. Epandrium, cerci and surstyli in dorsal view (setae omitted on left side). 11. Fifth abdominal sternite in ventral view (setae omitted on left side). 12. Hypandrium, pregonite, postgonite and phallus in lateral view. Abbreviations: cer, cercus; ep, epandrium; epi, epiphallus; hy, hypandrium; ph, phallus; pos, postgonite; pre, pregonite; sur, surstylus. Scale bars = 0.1 mm.
FIGURE 1 in A new species of Medinodexia Townsend (Diptera: Tachinidae) from Japan, with a discussion on phylogenetic implications of the female postabdomen in Blondeliini
FIGURE 1. Female of Medinodexia japonica sp. nov. in ventral view (paratype, Nishiaburayama, Fukuoka Prefecture, BLKU), with white arrows indicating blunt setae on hind coxae and trochanters. Scale bar = 0.2 mm.
FIGURES 17–20. Female postabdomens. 17–18 in A new species of Medinodexia Townsend (Diptera: Tachinidae) from Japan, with a discussion on phylogenetic implications of the female postabdomen in Blondeliini
FIGURES 17–20. Female postabdomens. 17–18. Medinodexia japonica sp. nov. (paratype, Kyushu University Ito Campus, Fukuoka Prefecture, BLKU). 17. Sixth abdominal tergite in dorsal view. 18. Postabdomen in lateral view. 19–20. Medina separata (Meigen) (Hokkaido, Japan, BLKU). 19. Sixth abdominal tergite in dorsal view. 20. Postabdomen in lateral view. Abbreviations: sg 7, seventh abdominal segment st 5, fifth abdominal sternite; st 6, sixth abdominal sternite; t 6, sixth abdominal tergite. Scale bars = 0.2 mm.
Systematic assessment of tumour purity and its clinical implications
<p>Supplemental data for the study: Systematic assessment of tumour purity and its clinical implications</p>
Transcriptome association studies of neuropsychiatric traits in African Americans implicates PRMT7 in schizophrenia
<p>Genome-wide association study of Schizophrenia and Bipolar Disorder in African Americans 2019</p>
FIGURE 14. Consensus tree obtained from a 847 in The identity of some specimens previously (mis)identified as Rhinoleucophenga obesa (Loew) (Diptera: Drosophilidae) in Brazil, based on morphological and molecular data, with implications on distribution
FIGURE 14. Consensus tree obtained from a 847-bp alignment of cytochrome c oxidase subunit I (COI) gene sequences of Rhinoleucophenga specimens. Above the branches, support values by Neighbour-joining (10,000 bootstrap replications) and posterior probabilities values using Bayesian inference (1,000,000 generations), respectively.
FIGURE 13 in The identity of some specimens previously (mis)identified as Rhinoleucophenga obesa (Loew) (Diptera: Drosophilidae) in Brazil, based on morphological and molecular data, with implications on distribution
FIGURE 13. Female terminalia of an typical specimen of R. cantareira from Porto de Galinhas, Pernambuco. a: ventral view; b: spermathecal capsule; c: dorsal view (scale bar 0.1 mm). c: cercus, e: epiproct,h: hypoproct, S6: sternite 6, S7: sternite 7, T6: tergite 6, T7: tergite 7.
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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.