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190 results for “NW China”
High-resolution and full coverage AOD downscaling based on the bagging model over the arid and semi-arid areas, NW China
<p>High-resolution and full coverage 250 m monthly AOD product over the arid and semi-arid areas, NW China. the scale factor is 1000.</p>
Data for: Variation in eye lenses of two new Late Devonian phacopid trilobites from western Junggar, NW China
<p>The Suborder Phacopina, characterized by schizochroal eyes, is among the most common groups of trilobites in Devonian strata. The marine sediments of the Famennian in western Junggar, Xinjiang, contain abundant low-disparity phacopids, which have previously been designated to <em>Omegops</em> <em>accipitrinus</em> <em>mobilis</em>, <em>Phacops</em> <em>circumspectans</em> <em>tuberculosus</em>, and <em>Omegops</em> <em>cornelius</em>, based on small numbers of poorly preserved specimens. In this study, these phacopids were identified as two new species of <em>Omegops</em>, <em>O</em>. <em>honggulelengensis</em> sp. nov. and <em>O</em>. <em>xiangi</em> sp. nov., based on nearly 200 well-preserved specimens. The intraspecific variations of eye-lenses of these specimens were quantitatively analyzed. Based on differences in the total number, number of dorso-ventral files, and arrangement of the eye lenses, the absence of lenses in the middle part of the visual surface, and asymmetry of the number and/or arrangement of lenses in the two eyes, it was concluded that the reasons for intraspecific variation in eye lenses of Late Devonian <em>Omegops</em> from western Junggar were different from previously described factors, but were likely genetic or embryological malfunctions, or abnormalities caused by pathological conditions. Diversity of lenses in the schizochroal eyes shows that the number and arrangement of eye lenses were not stable in Phacopina. Therefore, many specimens are needed for quantitative study to determine the true characteristics of the number or arrangement of eye lenses when these features are used in the systematic taxonomy of Phacopina.</p>
Data for: Variation in eye lenses of two new Late Devonian phacopid trilobites from western Junggar, NW China
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FIGURES 38–48 in Sexual variation in two species of Helorus Latreille (Hymenoptera, Heloridae) from NW China, with description of female of Helorus caii He & Xu
FIGURES 38–48. Helorus caii He & Xu, ♂, China (Shaanxi). 38 antenna. 39 head, anterior aspect. 40 mesosoma, lateral aspect. 41 propodeum and first tergite, lateral aspect. 42 metasoma, dorsal aspect. 43 wings. 44 head, dorsal aspect. 45 mesosoma, dorsal aspect. 46 first tergite, dorsal aspect. 47 metasoma, lateral aspect. 48 hind leg, lateral aspect.
FIGURES 50–58 in Sexual variation in two species of Helorus Latreille (Hymenoptera, Heloridae) from NW China, with description of female of Helorus caii He & Xu
FIGURES 50–58. Helorus caii He & Xu, ♀, China (Shaanxi). 50 head, dorsal aspect. 51 antenna, head and mesosoma, lateral aspect. 52 propodeum and first tergite, lateral aspect. 53 first tergite, dorsal aspect. 54 metasoma, lateral aspect. 55 head, anterior aspect. 56 mesosoma, dorsal aspect. 57 wings. 58 hind leg, lateral aspect.
FIGURES 14–24 in Sexual variation in two species of Helorus Latreille (Hymenoptera, Heloridae) from NW China, with description of female of Helorus caii He & Xu
FIGURES 14–24. Helorus antefurcalis He & Xu, ♂, China (Shaanxi). 14 antenna. 15 head, dorsal aspect. 16 mesosoma, dorsal aspect. 17 propodeum and first tergite, lateral aspect. 18 first tergite, dorsal aspect. 19 metasoma, lateral aspect. 20 metasoma, dorsal aspect. 21 head, anterior aspect. 22 mesosoma, lateral aspect. 23 wings. 24 hind leg, lateral aspect.
FIGURES 2–12 in Sexual variation in two species of Helorus Latreille (Hymenoptera, Heloridae) from NW China, with description of female of Helorus caii He & Xu
FIGURES 2–12. Helorus antefurcalis He & Xu, ♀, China (Shaanxi). 2 antenna. 3 mesosoma, lateral aspect. 4 mesosoma, dorsal aspect. 5 first tergite, dorsal aspect. 6 propodeum and first tergite, lateral aspect. 7 metasoma, lateral aspect. 8 scapus and pedicellus. 9 head, dorsal aspect. 10 head, anterior aspect. 11 fore wing. 12 hind leg, lateral aspect.
FIGURES 26–36 in Sexual variation in two species of Helorus Latreille (Hymenoptera, Heloridae) from NW China, with description of female of Helorus caii He & Xu
FIGURES 26–36. Helorus caii He & Xu, ♀, China (Shaanxi). 26 antenna. 27 head, dorsal aspect. 28 mesosoma, dorsal aspect. 29 first tegite, dorsal aspect. 30 metasoma, lateral aspect. 31 hind leg, lateral aspect. 32 head, anterior aspect. 33 mesosoma, lateral aspect. 34 propodeum and first tergite, lateral aspect. 35 metasoma, dorsal aspect. 36 wings.
FIGURES 9–16. Butterflies. 9 in Lethe elwesi (Moore) stat. rev., a distinct species, with description of a new subspecies from NW Yunnan, China (Lepidoptera, Nymphalidae, Satyrinae)
FIGURES 9–16. Butterflies. 9, Lethe elwesi stat. rev., male (Bhutan), dorsal; 10, ditto, ventral; 11, L. jalaurida, male (Bhutan), dorsal; 12, ditto, ventral; 13, L. jalaurida, male (Bhutan), dorsal; 14, ditto, ventral; 15, L. jalaurida nuolaensis, male, SATY0361 (Gongshan, Yunnan), dorsal (left) and ventral (right); 16, L. jalaurida plistia, male, SATY0367 (Puge, Sichuan), dorsal (left) and ventral (right). Scale bar = 10 mm.
FIGURES 35–38. 35 in Lethe elwesi (Moore) stat. rev., a distinct species, with description of a new subspecies from NW Yunnan, China (Lepidoptera, Nymphalidae, Satyrinae)
FIGURES 35–38. 35. Habitat of Lethe elwesi houjiangae ssp. nov. and L. jalaurida nuolaensis, altitude 3200 m, East slope of Mts. Gao-li-gong, Gongshan, NW Yunnan; 36. Habitat of L. elwesi stat. rev., altitude 2800 m, 62K, Medog, SE Tibet; 37. L. elwesi houjiangae ssp. nov. in nature, altitude 3200 m, Gongshan, NW Yunnan; 38. L. elwesi stat. rev. in nature, altitude 2800 m, 62K, Medog, SE Tibet.
FIGURES 23–28 in Lethe elwesi (Moore) stat. rev., a distinct species, with description of a new subspecies from NW Yunnan, China (Lepidoptera, Nymphalidae, Satyrinae)
FIGURES 23–28. Tip of the male valva in dorsal view. 23, Lethe elwesi houjiangae ssp. nov., holotype, SATY0369 (Gongshan, Yunnan); 24, L. elwesi houjiangae ssp. nov., paratype, SATY0356 (Gongshan, Yunnan); 25, L. elwesi houjiangae ssp. nov., paratype, SATY0363 (Gongshan, Yunnan); 26, L. elwesi stat. rev., SATY0368 (Medog, Tibet); 27, L. jalaurida nuolaensis, SATY0361 (Gongshan, Yunnan); 28, L. jalaurida plistia, SATY0367 (Puge, Sichuan).
FIGURES 1–8. Butterflies. 1 in Lethe elwesi (Moore) stat. rev., a distinct species, with description of a new subspecies from NW Yunnan, China (Lepidoptera, Nymphalidae, Satyrinae)
FIGURES 1–8. Butterflies. 1, Lethe elwesi houjiangae ssp. nov., male, holotype, SATY0369 (Gongshan, Yunnan), dorsal; 2, ditto, ventral; 3, L. elwesi houjiangae ssp. nov., male, paratype, SATY0356 (Gongshan, Yunnan), dorsal; 4, ditto, ventral; 5, L. elwesi houjiangae ssp. nov., male, paratype (Gongshan, Yunnan), dorsal; 6, ditto, ventral; 7, L. elwesi stat. rev., male, SATY0368 (Medog, Tibet), dorsal; 8, ditto, ventral. Scale bar = 10 mm.
FIGURES 17–22. Male genitalia. a in Lethe elwesi (Moore) stat. rev., a distinct species, with description of a new subspecies from NW Yunnan, China (Lepidoptera, Nymphalidae, Satyrinae)
FIGURES 17–22. Male genitalia. a. Male genitalia in lateral view with left valva and aedeagus removed; b. Aedeagus in lateral view. 17, Lethe elwesi houjiangae ssp. nov., holotype, SATY0369 (Gongshan, Yunnan); 18, L. elwesi houjiangae ssp. nov., paratype, SATY0356 (Gongshan, Yunnan); 19, L. elwesi houjiangae ssp. nov., paratype, SATY0363 (Gongshan, Yunnan); 20, L. elwesi stat. rev., SATY0368 (Medog, Tibet); 21, L. jalaurida nuolaensis, SATY0361 (Gongshan, Yunnan); 22, L. jalaurida plistia, SATY0367 (Puge, Sichuan).
FIGURES 1–8 in Description of a new species of Chonala (Lepidoptera, Nymphalidae, Satyrinae) from NW Yunnan, China
FIGURES 1–8. Butterflies of Chonala. 1, C. huertasae sp. nov., male, holotype (Gongshan, Yunnan), upperside; 2, ditto, underside; 3, C. praeusta burmana, male (Gongshan, Yunnan), upperside; 4, ditto, underside; 5, C. yunnana, male (Shangri-la, Yunnan), upperside; 6, ditto, underside; 7, C. masoni, male (Bhumtang, Bhutan), upperside; 8, ditto, underside.
FIGURES 9–10. Male genitalia. a in Description of a new species of Chonala (Lepidoptera, Nymphalidae, Satyrinae) from NW Yunnan, China
FIGURES 9–10. Male genitalia. a. Male genitalia in lateral view with left valva and aedeagus removed; b. Aedeagus in lateral view; c. Tip of the male valva in dorsal view. 9, Chonala huertasae sp. nov., holotype (Gongshan, Yunnan); 10, C. praeusta burmana (Gongshan, Yunnan).
FIGURES 13–16. 13 in Description of a new species of Chonala (Lepidoptera, Nymphalidae, Satyrinae) from NW Yunnan, China
FIGURES 13–16. 13. Chonala huertasae sp. nov., male, paratype, in net, Gongshan, NW Yunnan, upperside; 14. ditto, underside in lateral view; 15. Habitat of C. huertasae sp. nov., altitude 2800 m, Dulong Valley, Mts. Gao-li-gong, Gongshan, NW Yunnan; 16. ditto.
FIGURE 1. A–B in Recent brachiopods from the South China Sea, NW Pacific
FIGURE 1. A–B. Terebratulina japonica (Sowerby, 1846), dorsal views of complete specimens, stn DW 4125, 305–306 m, SEM, MNHN IB-2013-640. C–G. Macandrevia sp., one complete specimen, stn CP 4123, 1612–1665 m, MNHN IB-2013-641. C–D. Dorsal and lateral views of complete specimen. E–F. Ventral valve of the same specimen, posterior part of interior and tilted view to show strong dental plates, SEM. G. Interior view of dorsal valve to show cardinalia, SEM. H–R. Nipponithyris afra Cooper, 1973, stn CP 4130, 795–822 m. H–M. Dorsal, lateral and anterior views of two complete specimens, MNHN BI-2013-642. N–O. Posterior part of ventral valve interior and tilted view to show swollen bases and grooves to accommodate inner socket ridges, SEM, MNHN BI-2013- 643. P. Interior of dorsal valve, partly broken loop visible, SEM, MNHN BI-2013-644. Q–R. Posterior part of dorsal valve interior and enlargement to show details of strongly thickened cardinalia, SEM MNHN BI-2013-645.
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V_ v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas). in Canidae
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V_ v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas).
Subspecies and Distribution. A. f. fulgens Cuvier, 1825 — E Himalayas in Bhutan, India, Nepal, Sikkim; China (S & SE Xizang & NW Yunnan), NE India (Meghalaya), and N Myanmar. A. f. styani Thomas, 1902 — China (W Sichuan & N Yunnan). in Ailuridae
Subspecies and Distribution. A. f. fulgens Cuvier, 1825 — E Himalayas in Bhutan, India, Nepal, Sikkim; China (S & SE Xizang & NW Yunnan), NE India (Meghalaya), and N Myanmar. A. f. styani Thomas, 1902 — China (W Sichuan & N Yunnan).
Subspecies and Distribution. V. i. indica Geoffroy Saint-Hilaire, 1803 — S peninsular India. V. i. atchinensis Sody, 1931 — Sumatra. V. i. baliensis Sody, 1931 — Bali. V. i. baptistae Pocock, 1933 — Bangladesh to NE India (Assam), and Bhutan. V. i. deserti Bonhote, 1898 — Pakistan through C India to Nepal. V. i. klossi Pocock, 1933 — Malaysia. V. i. mayori Pocock, 1933 — Sri Lanka. V. i. muriavensis Sody, 1931 — Java. V.i. taivana Schwarz, 1911 — Taiwan. V.i. thai Kloss, 1919 — Myanmar and Thailand through Indochina to China. V. i. wellsi Pocock, 1933 — NW India. It has been introduced to Madagascar, Zanzibar Island, the Comoro Islands, and Socotra Island for the production of civet or to be used as rat catchers; its presence on some of the Indonesian islands (Bali, Bawean, Kangean, Lombok, and Sumbawa) could also have resulted from introductions. in Viverridae
Subspecies and Distribution. V. i. indica Geoffroy Saint-Hilaire, 1803 — S peninsular India. V. i. atchinensis Sody, 1931 — Sumatra. V. i. baliensis Sody, 1931 — Bali. V. i. baptistae Pocock, 1933 — Bangladesh to NE India (Assam), and Bhutan. V. i. deserti Bonhote, 1898 — Pakistan through C India to Nepal. V. i. klossi Pocock, 1933 — Malaysia. V. i. mayori Pocock, 1933 — Sri Lanka. V. i. muriavensis Sody, 1931 — Java. V.i. taivana Schwarz, 1911 — Taiwan. V.i. thai Kloss, 1919 — Myanmar and Thailand through Indochina to China. V. i. wellsi Pocock, 1933 — NW India. It has been introduced to Madagascar, Zanzibar Island, the Comoro Islands, and Socotra Island for the production of civet or to be used as rat catchers; its presence on some of the Indonesian islands (Bali, Bawean, Kangean, Lombok, and Sumbawa) could also have resulted from introductions.
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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.