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119 results for “Yi”
Figure 8 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 8 Relative synonymous codon usage (RSCU) of the mitogenomes of the five Trichiurus species; the stop codon is not included. T. japonicus (TJ), T. lepturus (TL), T. nanhaiensis (TN), T. gangeticus (TG) and T. brevis (TB).
Figure 7 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 7 A Mean evolutionary rates for each protein coding gene in mitogenomes of five Trichiurus species B Evolutionary rates of ND6 gene of five Trichiurus species. C Evolutionary rates of Ka/Ks in ATP8 gene of five Trichiurus species. Indicated the rates of non-synonymous substitutions to the rate of synonymous substitutions (ka/ks). T. japonicus (TJ), T. lepturus (TL), T. nanhaiensis (TN), T. gangeticus (TG) and T. brevis (TB).
Figure 2 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 2 Positions of 14 (a–n) landmarks used to contrast the morphological differences between Trichiurus species.
Supplementary material 1 from: Lin S-S, Li Y-H, Su H-L, Yi H, Pan Z, Sun Y-J, Zeng Z-C, Wang J (2022) Discovery of a new limestone karst-restricted odorous frog from northern Guangdong, China (Anura, Ranidae, Odorrana). ZooKeys 1120: 47-66. https://doi.org/10.3897/zookeys.1120.87067
Table S1
Figure 4 from: Zhao L, Yi D, Li C, Sun D, Xu H, Gao T (2017) Phylogeography and population structure of - grypotus (Richardson, 1846) as revealed by mitochondrial control region sequences. ZooKeys 705: 143-158. https://doi.org/10.3897/zookeys.705.13001
Figure 4 - Observed and expected mismatch distribution under the sudden expansions model of the control region haplotypes in J. grypotus.
Figure 3 from: Zhao L, Yi D, Li C, Sun D, Xu H, Gao T (2017) Phylogeography and population structure of - grypotus (Richardson, 1846) as revealed by mitochondrial control region sequences. ZooKeys 705: 143-158. https://doi.org/10.3897/zookeys.705.13001
Figure 3 - Minimum spanning network showing genetic relationship among mtDNA control region haplotypes in J. grypotus (Circles represent haplotypes with sizes proportional to their respective frequencies. Tick marks represent deduced numbers of nucleotide substitutions along each branch)
Figure 2 from: Zhao L, Yi D, Li C, Sun D, Xu H, Gao T (2017) Phylogeography and population structure of - grypotus (Richardson, 1846) as revealed by mitochondrial control region sequences. ZooKeys 705: 143-158. https://doi.org/10.3897/zookeys.705.13001
Figure 2 - Phylogenetic tree of control region haplotypes constructed using neighbor-joining algorithms of J. grypotus.
Figure 5 from: Zhao L, Yi D, Li C, Sun D, Xu H, Gao T (2017) Phylogeography and population structure of - grypotus (Richardson, 1846) as revealed by mitochondrial control region sequences. ZooKeys 705: 143-158. https://doi.org/10.3897/zookeys.705.13001
Figure 5 - Bayesian skyline plots showing NefT (Nef=effective female population size; T=generation time) changes through time in J. grypotus populations. Black lines are median estimates of NefT; light lines represent the upper and lower 95% highest posterior density (HPD) limits of NefT.
BESHIK TO'YI MAROSIMI FOLKLORINING O'RGANILISHIGA DOIR
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Figure 6 from: Li Q, Hu H, Triapitsyn S, Yi L, Lu J (2018) Anagrus dmitrievi sp. n. (Hymenoptera, Mymaridae), an egg parasitoid of Zyginidia eremita (Hemiptera, Cicadellidae), a pest of maize in Xinjiang, China. ZooKeys 736: 43-57. https://doi.org/10.3897/zookeys.736.20883
Figure 6 Records of Zyginidia eremita in Xinjiang. The large star denotes the type locality of Anagrus dmitrievi.
Figure 2 from: Li Q, Hu H, Triapitsyn S, Yi L, Lu J (2018) Anagrus dmitrievi sp. n. (Hymenoptera, Mymaridae), an egg parasitoid of Zyginidia eremita (Hemiptera, Cicadellidae), a pest of maize in Xinjiang, China. ZooKeys 736: 43-57. https://doi.org/10.3897/zookeys.736.20883
Figure 2 Anagrus dmitrievi (female, holotype): A ovipositor (arrows pointing to distal setae on one of its external plates, or second valvifers) B fore and hind wings.
Figure 1 from: Li Q, Hu H, Triapitsyn S, Yi L, Lu J (2018) Anagrus dmitrievi sp. n. (Hymenoptera, Mymaridae), an egg parasitoid of Zyginidia eremita (Hemiptera, Cicadellidae), a pest of maize in Xinjiang, China. ZooKeys 736: 43-57. https://doi.org/10.3897/zookeys.736.20883
Figure 1 Anagrus dmitrievi (female, holotype): A slide B antennae (complete antenna without mps on F4; F4 of the incomplete antenna with 1 mps) C body D mesoscutum (arrows pointing to adnotaular setae on its midlobe).
Figure 4 from: Li Q, Hu H, Triapitsyn S, Yi L, Lu J (2018) Anagrus dmitrievi sp. n. (Hymenoptera, Mymaridae), an egg parasitoid of Zyginidia eremita (Hemiptera, Cicadellidae), a pest of maize in Xinjiang, China. ZooKeys 736: 43-57. https://doi.org/10.3897/zookeys.736.20883
Figure 4 A parasitized eggs of Zyginidia eremita by Anagrus dmitrievi in a maize leaf B an adult female of A. dmitrievi right after emergence C an adult male of A. dmitrievi.
FIGURE 12 in A remarkable new species of Nemoura (Plecoptera: Nemouridae) from Chuxiong Yi Autonomous Prefecture of Yunnan Province, China
FIGURE 12. Type locality, Zixi Mountain, Chuxiong Yi Autonomous Prefecture, Yunnan Province, China.
Supplementary material 6 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
File S2. Checklist of the species of Neuroptera from Beijing :
Supplementary material 5 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
File S1. List of all specimens used in this study, including GenBank accession numbers :
Figure 1 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
Figure 1 Neighbor-joining tree based on the COI sequence dataset of the lacewing species from Beijing. Different color of clades represents different species.
Figure 4 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
Figure 4 Habitus photographs of species of Hemerobiidae newly recorded from Beijing. ADrepanepteryxalgida (Erichson, 1851) BHemerobiusbispinus Banks, 1940 CHemerobiusexoterus Navás, 1936 DHemerobiushumulinus Linnaeus, 1758 EHemerobiusjaponicus Nakahara, 1915 FHemerobiusmarginatus (Stephens, 1836) GHemerobiussubtriangulus Yang, 1987 HSympherobiusmanchuricus Nakahara, 1960. Scale bar: 1 mm.
Figure 3 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
Figure 3 Habitus photographs of species of Chrysopidae newly recorded from Beijing. ANothochrysasinica Yang, 1986 BChrysopaintima McLachlan, 1893 CChrysoperlafurcifera (Okamoto, 1914) DChrysopidiaciliata (Wesmael, 1841) EMalladaflavimaculus Yang & Yang, 1991 FPseudomalladacognatellus (Okamoto, 1914) GPseudomalladaqinlingensis (Yang & Yang, 1989) HNinetagrandis Navás, 1915 INinetashaanxiensis Yang & Yang, 1989. Scale bar: 1 mm.
Figure 2 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
Figure 2 Habitus photographs of species of Coniopterygidae newly recorded from Beijing. AConwentziasinica Yang, 1974 BSemidalisbicornis Liu & Yang, 1993. Scale bar: 1 mm.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.