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9,029 results for “Asia”
FIGURE 4 in The water mite family Aturidae Thor, 1900 from Southeast Asia (Acari: Hydrachnidia) with the description of one new genus and 14 new species
FIGURE 4: Hexaxonopsis reticulata n. sp., A – C holotype male, D – paratype female: A – dorsum; B – venter; C – palp; D – venter. Scale bars = 50 µm.
FIGURE 3 in The water mite family Aturidae Thor, 1900 from Southeast Asia (Acari: Hydrachnidia) with the description of one new genus and 14 new species
FIGURE 3: Brachypodopsis thailandicus n. sp., holotype female: A – dorsum; B – venter; C – palp. Scale bars = 50 µm.
FIGURE 1 in The water mite family Aturidae Thor, 1900 from Southeast Asia (Acari: Hydrachnidia) with the description of one new genus and 14 new species
FIGURE 1: Albaxonona elongata n. sp., holotype female: A – dorsum; B – venter; C – palp. Scale bars = 50 µm.
Figs. 4 in Oculogryphus, A Remarkable New Genus of Fireflies from Asia (Coleoptera: Lampyridae)
Figs. 4. Oculogryphus fulvus, new genus and species, male, head and thorax, ventral aspect.
Fig. 5 in Oculogryphus, A Remarkable New Genus of Fireflies from Asia (Coleoptera: Lampyridae)
Fig. 5. Oculogryphus fulvus, new genus and species, male, basal half of elytra, lateral aspect.
Figure 3 Alhagi maurorum, plant with typical Aceria alhagi n in A new Aceria species (Acari:Trombidiformes: Eriophyoidea) from West Asia, a potential biological control agent for the invasive weed camelthorn, Alhagi maurorum Medik. (Leguminosae)
Figure 3 Alhagi maurorum, plant with typical Aceria alhagi n. sp. symptoms where the shoot tips
Figure 3 in Revision of Acanthocyrtus (Collembola: Entomobryidae), with description of a new genus from eastern Asia
Figure 3. Cephalic dorsal chaetotaxy (Mari-Mutt, 1986).
Figure 1 in Revision of Acanthocyrtus (Collembola: Entomobryidae), with description of a new genus from eastern Asia
Figure 1. Biogeographical map of species distribution of Acanthocyrtus.
Hydroclimate of the Tibetan Plateau and Central Asia during the Late Cenozoic
<p>These repository data contain netcdf files for each of the four high-resolution (~0.75° per grid cell) general circulation model (GCM) ECHAM-5 experiments with boundary conditions for the mid-Pliocene (~3 Ma; ECHAM5_PLIO_1d_aprl_aprc_q_v_u_Asia.nc), the Last Glacial Maximum (LGM; ~21 ka; ECHAM5_LGM_1d_aprl_aprc_q_v_u_Asia.nc), the mid-Holocene (~6 ka; ECHAM5_MH_1d_aprl_aprc_q_v_u_Asia.nc), and the pre-industrial (ECHAM5_PI_1d_aprl_aprc_q_v_u_Asia.nc). Each file contains 3D fields of specific humidity and winds, as well as precipitation (large-scale and convective) for Asian region. </p>
Laboratory bioassay of insecticides mixtures (neonicotinoids and ketoenols) against Bemisia tabaci Asia I
<p>Cotton leaves were dipped in serially diluted solutions of formulated insecticides for 10 s with slight agitation. The leaves with second instar nymphs that were dipped in double-distilled water containing 0.1 g L<sup>-1</sup> Triton X-100 only, served as control. Each bioassay including control used 3-4 replicates at a minimum of eight different concentrations and were maintained at the controlled growth condition. All the insecticides concentrations were selected to give a range of 0-100% mortality of <em>B. tabaci</em> nymphs. Two weeks later final mortality was assessed when the last nymphal instar had been reached on control plants. It was computed by comparing the number of second instar nymphs present at the time of treatment with the number remaining dead or unhatched on the day of mortality assessment. For bioassays with synergists (PBO and DEF), the cotton leaves containing the second instar nymphs of <em>B. tabaci</em> were dipped into synergist solutions (100 mg L<sup>-1</sup>) for 10 s at least 2 h before the imposition of insecticide treatments. Other procedures were same to those with insecticides only.</p>
A regionally resolved inventory of High Mountain Asia surge-type glaciers, derived from a multi-factor remote sensing approach
<p>This file is the .csv database compiling surge-type glaciers automatically identified in Guillet et al (2022).</p> <p>File format is compliant with the Randolph Glacier Inventory (RGI) V6.0.</p> <p>If you have questions about the dataset - please refer to the following reference or contact Dr. Guillet.</p> <table> <tbody> <tr> <td>Guillet, G., King, O., Lv, M., Ghuffar, S., Benn, D., Quincey, D., & Bolch, T. (2022). A regionally resolved inventory of High Mountain Asia surge-type glaciers, derived from a multi-factor remote sensing approach. <em>The Cryosphere</em>, <em>16</em>(2), 603-623.</td> </tr> <tr> <td> </td> </tr> </tbody> </table> <p> </p>
Ancient volcanos as species pumps: A case study of freshwater amphipods in Northeast Asia
<p>Volcano-tectonic processes have been viewed as primary divers in the formation of present-day diversity. Volcanos associated with mountain uplifts drives allopatric speciation through vicariance and may impact the surrounding areas like species pump or species attractor. However, the application of these hypotheses to aquatic fauna has rarely been tested explicitly. We conducted this research in the Changbai Mountains (Mts), which are one of the most typical, active volcanic ranges in Northeast (NE) Asia with a long and turbulent geological history. The <i>Gammarus nekkensis</i> species complex of amphipod crustaceans, widely distributed throughout NE Asia with poor dispersal abilities and a long evolutionary history, is a suitable model for testing these hypotheses. Phylogenetic and ancestral range reconstructions demonstrated that the studied amphipod originated from the Changbai Mts approximately 27 Ma and diverged into eastern (Clade I) and western (Clade II) clades, which corresponds well with the initial volcanic eruption of the Changbai Mts in the Late Oligocene. The subsequent diversifications of subclades CI-3, CII-1a and CII-2a were likely driven by second and third eruptions of the Changbai Mts during the Miocene. In particular, the Changbai lineages had spread to the Russian Far East multiple times since the Early Miocene, and widely colonized the region during the Pleistocene. Our discoveries suggest that the ancient volcanos of the Changbai Mts act as species pumps in NE Asia, resulted in burst of diversification around the Changbai Mts and subsequent dispersals into adjacent regions.</p>
57 Block--63k or 50k scale Maps of South Asia--additional 2--20251024
<p>89 new map files to add to the set of 63k/50k Maps of South Asia, Block 57. An updated Index Map for Block 57 is included in this set of maps.</p>
63 Block--63k or 50k scale Maps of South Asia--additional 2--20251024
<p>96 new map files to add to the set of 63k/50k Maps of South Asia, Block 63. An updated Index Map for Block 63 is included in this set of maps.</p>
56 Block--63k or 50k scale Maps of South Asia--additional 2--20251024
<p>13 new map files to add to the set of 63k/50k Maps of South Asia, Block 56. An updated Index Map for Block 56 is included in this set of maps.</p>
53 Block--63k or 50k scale Maps of South Asia--additional 1--20251024
<p>99 new map files to add to the set of 63k/50k Maps of South Asia, Block 53. An updated Index Map for Block 53 is included in this set of maps.</p>
39 Block--63k or 50k scale Maps of South Asia--additional 2--20251024
<p>48 new map files to add to the set of 63k/50k Maps of South Asia, Block 39. An updated Index Map for Block 39 is included in this set of maps.</p>
43 Block--63k or 50k scale Maps of South Asia--additional 2--20251024
<p>89 new map files to add to the set of 63k/50k Maps of South Asia, Block 43. An updated Index Map for Block 43 is included in this set of maps.</p>
79 Block--63k or 50k scale Maps of South Asia--additional 1--20240105
<p>77 new map files to add to the set of 63k/50k Maps of South Asia, Block 79. An updated Index Map for Block 79 is included in this set of maps.</p>
47 Block--63k or 50k scale Maps of South Asia--additional 1--20251024
<p>56 map files of add to the set of 63k/50k Maps of South Asia, Block 47. An updated Index Map for Block 47 is included in this set of maps.</p>
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)
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.