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2,402 results for “East Asia”
Subspecies and Distribution. S.e.etruscusSavi,1822—EuropeandCaucasus;thissubspeciesprobablyalsoinTurkey(scatteredrecordsinW,N&SC). S.e.bactrianusStroganov,1958—Tajikistan. S.e.madagascariensisCoquerel,1848—Madagascar. S.e.micronyxBlyth,1855—Himalayas. S.e.nanulaStroganov,1941—Uzbekistan. S.e.nudipesBlyth,1855—NEIndia. S. e. perrottetti Duvernoy, 1842 — S India. Also known from Tenerife I, many Mediterranean Is, North Africa, Arabia, Socotra I, and Central and South-east Asia, but subspecies involved not known. in Soricidae
Subspecies and Distribution. S.e.etruscusSavi,1822—EuropeandCaucasus;thissubspeciesprobablyalsoinTurkey(scatteredrecordsinW,N&SC). S.e.bactrianusStroganov,1958—Tajikistan. S.e.madagascariensisCoquerel,1848—Madagascar. S.e.micronyxBlyth,1855—Himalayas. S.e.nanulaStroganov,1941—Uzbekistan. S.e.nudipesBlyth,1855—NEIndia. S. e. perrottetti Duvernoy, 1842 — S India. Also known from Tenerife I, many Mediterranean Is, North Africa, Arabia, Socotra I, and Central and South-east Asia, but subspecies involved not known.
Distribution. Mainland South-east Asia in S Laos (N limit is 16° 23' N), SC Vietnam (N limit is 14° 30' N), and E Cambodia (Ratanakiri and Mondulkiri provinces); most likely the W limitis the Mekong River, but further studies are needed to confirm this. Records in Vietnam N to 16° 37° N are questionable. in Cercopithecidae
Distribution. Mainland South-east Asia in S Laos (N limit is 16° 23' N), SC Vietnam (N limit is 14° 30' N), and E Cambodia (Ratanakiri and Mondulkiri provinces); most likely the W limitis the Mekong River, but further studies are needed to confirm this. Records in Vietnam N to 16° 37° N are questionable.
Distribution. Mainland South-east Asia in S Myanmar, S Thailand, S Laos, Cambodia (W of Mekong River), and the S tip of Vietnam. Range limit of this species to the E might be the Mekong River. in Cercopithecidae
Distribution. Mainland South-east Asia in S Myanmar, S Thailand, S Laos, Cambodia (W of Mekong River), and the S tip of Vietnam. Range limit of this species to the E might be the Mekong River.
Improvement of the aerosol forecast and analysis over East Asia with joint assimilation of two geostationary satellite observations
<p>These are FY-4A satellite AOD products and SONET AOD datasets used in the manuscript titled "Improvement of the aerosol forecast and analysis over East Asia with joint assimilation of two geostationary satellite observations" to Geophysical Research Letters. </p>
Figure 11 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 11. Illustration showing how marine incursion could drive sea–land transition and diversification of the M. japonica complex. A, marine incursion leads to large-scale sea–land transition. B, isolation caused by subsequent marine regression drives terrestrial species diversification. C, stepping-stone dispersal maintains gene flow between different regions. Arrows show the direction of dispersal.
Figure 10 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 10. Morinoia aosen sp. nov. female paratype, from Beijing. A, antennae I–II. B, gnathopod I. C, gnathopod II. D, propodus of gnathopod II. E, pleopod. F, the tip of spine (on the propodus of gnathopod II).
Figure 9 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 9. The telson in Morinoia species. A, B, telson of Morinoia aosen sp. nov. C, telson of M. paludosus. D, telson of M. japonica. White arrows show the interspecific difference. Images of M. paludosus and M. japonica modified from Cheng et al. (2011).
Figure 7 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 7. Morinoia aosen sp. nov. male holotype, from Beijing. A, pereopod III. B, pereopod IV. C, pereopod V. D, pereopod VI. E, pereopod VII.
Figure 8 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 8. The uropod III in Morinoia species. A, B, uropod III of Morinoia aosen sp. nov. C, D, uropod III of M. japonica. E–G, uropod III of M. paludosus. White arrows show the interspecific difference and black arrows show the intraspecific difference. Images of M. paludosus and M. japonica modified from Cheng et al. (2011).
Figure 3 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 3. Population structure of Morinoia japonica species complex based on COI haplotypes. A, minimum spanning network. Each circle represents a unique mitochondrial COI haplotype, with size proportional to frequency. B, assignment of 89 COI haplotypes to K = 5 genetic clusters inferred from STRUCTURE simulations. Colours indicate posterior probability of assignment of each individual to a particular cluster based on the combination of ten replicate runs.
Figure 4 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 4. Morinoia aosen sp. nov. from Beijing. A, male, holotype, IZCAS-I-A1700–1, 8.5 mm. B, female, paratype, IZCASI-A1700–2, 7.6 mm.
Figure 1 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 1. Map of East Asia showing sampling sites. Different-coloured dots correspond to different species delimited by ABGD: Morinoia aosen sp. nov. (red), M. paludosus (green), M. japonica (blue), M. sp1 (green), M. sp2 (pink), M. sp3 (light purple), M. sp4 (purple) and M. sp5 (yellow). White dots represent the coastal Platorchestia pacifica species complex.
Figure 2. A in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 2. A, time-calibrated tree obtained from BEAST 2 based on concatenated loci. The divergence times and 95% highest posterior density are showed at nodes of interest. The sea–land transition occurred about 15.63 Mya, corresponding with the divergence between coastal Platoechestia pacifica and terrestrial Morinoia japonica. The ancestral range reconstructions from the DEC+j model in BioGeoBEARS are indicated at the internal nodes. The bars and species at the right of the tree were inferred from species delimitation based on K2P distance. B, biogeographical reconstruction of stepping-stone dispersal in M. japonica from the Japanese islands to north-eastern continental China. C, sea-level fluctuations (blue line) modified from Miller et al. (2005). The light blue vertical shading indicates the Miocene marine incursion during a high sea-level period.
Figure 6 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 6. Morinoia aosen sp. nov. male holotype, from Beijing. A, antennae I–II. B, uropods. C, gnathopod I. D, gnathopod II. E, uropod I. F, uropod II.
Figure 5 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species
Figure 5. Morinoia aosen sp. nov. male holotype, from Beijing. A, upper lip. B, left mandible. C, right mandible. D–E, maxilla I. F, maxilla II. G, lower lip. H, maxilliped.
Unraveling hierarchical genetic structure of tea green leafhopper, Matsumurasca onukii, in East Asia based on SSRs and SNPs
<p><em>Matsumurasca onukii</em> (Matsuda, 1952), one of the dominant pests in major tea production areas in Asia, currently is known to occur in Japan, Vietnam, and China, and severely threatens tea production, quality, and international export trade. To elucidate the population genetic structure of this species, 1633 single nucleotide polymorphisms (SNPs) and 18 microsatellite markers (SSRs) were used to genotype samples from 27 sites representing 18 geographical populations distributed throughout the known range of the species in East Asia. Analyses of both SNPs and SSRs showed that <em>M</em>. <em>onukii</em> populations in Yunnan exhibit high genetic differentiation and structure compared to other populations. The Kagoshima (JJ) and Shizuoka (JS) populations from Japan were separated from populations from China by SNPs but clustered with Jinhua (JH), Yingde (YD), Guilin (GL), Fuzhou (FZ), Hainan (HQ), Leshan (CT), Chongqing (CY) and Zunyi (ZY) tea areas in China and the Vietnamese Vinh Phuc (VN) population based on SSR data. On the contrary, CT, CY, ZY, and Shaanxi (SX) populations clustered together based on SNPs, but were separated by SSRs. Both marker datasets identified significant geographic differentiation among the 18 populations. Various environmental and anthropogenic factors, including the geographical barriers to migration, human transport of hosts (<em>Camellia sinesis</em> (L.) O. Kuntze), and adaptability of <em>M. onukii</em> to various climatic zones possibly account for the rapid spread of this pest in Asia. The results demonstrate that SNPs from high-throughput genotyping data can be used to reveal subtle genetic substructure at broad scales in r-strategist insects.</p>
FIGURES 20–25 in New or little-known taxa of Anurophorinae (Collembola) with anal spines from East Asia with notes on DNA barcode
FIGURES 20–25. Distal part of abdomen in genera with four anal spines on Abd.V: 20–21, Tetracanthella, T. wahlgreni (20) and T. stebaevae (21); 22–23, Blissia, B. glabra, after Rusek (1985) (22) and B. robusta (23); 24, Sibiracanthella (S. rara), 25, Dimorphacanthella (D. mediaseta). Anterior row of setae notated as a1, Md, a3, Mdl. s—s-seta. Most of lateral setae not shown.
FIGURES 6–10 in New or little-known taxa of Anurophorinae (Collembola) with anal spines from East Asia with notes on DNA barcode
FIGURES 6–10. Sahacanthella saoriae sp. nov.: 6, PAO and ocelli; 7, medial conical protuberance, lateral view; 8, Abd.IV– VI; 9, distal part of tibiotarsus 3; 10, Ant.3, lateral view, variability shown. Md—dorsal macroseta, s—s-seta.
FIGURES 17–19 in New or little-known taxa of Anurophorinae (Collembola) with anal spines from East Asia with notes on DNA barcode
FIGURES 17–19. Distal part of abdomen in Octodonthophora ornata: 17–18, common variant with 9 spines, latero-dorsal (17) and latero-ventral (18) views; 19, small male with 8 spines, latero-dorsal views, most of lateral setae not shown. For the abbreviations see the text.
FIGURES 11–16 in New or little-known taxa of Anurophorinae (Collembola) with anal spines from East Asia with notes on DNA barcode
FIGURES 11–16. Octodonthophora ornata: 11, chaetotaxy of body tergites; 12. PAO and ocelli; 13, appearance and macrochaetotaxy; 14, furca; 15, Abd.IV–VI, dorsal view; 16, Th.II. Abbreviations as in Figs 1–5.
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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.