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2,256 results for “Southern China”
Fig. 9 in Cheniella gen. nov. (Leguminosae: Cercidoideae) from southern China, Indochina and Malesia
Fig. 9. Flowers of Cheniella tenuiflora (Watt ex C.B.Clarke) R.Clark & Mackinder comb. nov., showing yellow staminodal disc in young flower and dark pink staminodal disc in old flower. Photo: R. Clark.
Fig. 4 in Cheniella gen. nov. (Leguminosae: Cercidoideae) from southern China, Indochina and Malesia
Fig. 4. Illustration of Cheniella R.Clark & Mackinder gen. nov. A. Cheniella ovatifolia (T.C.Chen) R.Clark & Mackinder comb. nov., habit (Harder et al. 4249). B. C. glauca (Wall. ex Benth.) R.Clark & Mackinder comb. nov., leaf abaxial surface (Horsfield 165). C. C. quinnanensis subsp. villosa R.Clark & Mackinder subsp. nov., leaf abaxial indumentum (Tu 924). D. C. quinnanensis (T.C.Chen) R.Clark & Mackinder comb. nov. subsp. quinnanensis, leaf abaxial indumentum (Forrest 11844). E. C. tenuiflora (Watt ex C.B.Clarke) R.Clark & Mackinder comb. nov., flower (Urquhart s.n.). F. C. touranensis (Gagnep.) R.Clark & Mackinder comb. nov., flower (Henry 10175). G. C. touranensis, ovary (Harder & al. 2387). H. C. quinnanensis, ovary (Bar 2676). I. C. tenuiflora, fruit (Winit 1455). J. C. corymbosa (Roxb.) R.Clark & Mackinder comb. nov., fruit (Cult. Calcutta B.G. s.n.). K. C. corymbosa, seed, three views (Cult. Calcutta B.G. s.n.). L. C. tenuiflora, schematised flower, showing staminodes (2 broken), bases of 3 stamen filaments (solid black), base of ovary (dotted), bases of petals (dotted outlines), sepals and hairs omitted. Drawn by Andrew Brown.
Fig. 8 in Cheniella gen. nov. (Leguminosae: Cercidoideae) from southern China, Indochina and Malesia
Fig. 8. Nectariferous disc of Phanera championii Benth. (Clark 458). A. Whole disc ×30. B. Surface apertures ×450.
Fig. 6 in Cheniella gen. nov. (Leguminosae: Cercidoideae) from southern China, Indochina and Malesia
Fig. 6. Staminodes of Phanera yunnanensis (Franch.) Wunderlin, not joined at the base and lacking a fleshy disc (×35, Owens s.n.).
Fig. 10 in Cheniella gen. nov. (Leguminosae: Cercidoideae) from southern China, Indochina and Malesia
Fig. 10. Distribution of Cheniella glauca (Wall. ex Benth.) R.Clark & Mackinder comb. nov. and C. tenuiflora (Watt ex C.B.Clarke) R.Clark & Mackinder comb. nov.
Fig. 8 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 8. Coecobrya oculata sp. nov. A. Labrum. B. Dorsal cephalic chaetotaxy. C. Lateral process of labial palp. D. Chaetae on the ventral side of head. E. Trochanteral organ, ventral view. F. Hind claw. G. Anterior face of ventral tube and lateral flap. H. Posterior face of ventral tube. I. Mucro. J. Thoracic chaetotaxy. K–M, Abdominal chaetotaxy. K. Abd. I–III. L. Abd. IV. M. Abd. V. Scale bars: A, C–I = 20 μm; B, J–M = 100 μm.
Fig. 7 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 7. Abdominal chaetotaxy of Coecobrya ciliata sp. nov. A. Abd. I–III. B. Abd. IV. C. Abd. V. Scale bars: 50 μm.
Fig. 6 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 6. Coecobrya ciliata sp. nov. A. Ant. III organ. B. Dorsal cephalic chaetotaxy. C. Lateral process of labial palp. D. Chaetae on the ventral side of head. E. Trochanteral organ, ventral view. F. Hind claw. G. Anterior face of ventral tube ad lateral flap. H. Posterior face of ventral tube. I. Mucro. J. Thoracic chaetotaxy. Scale bars: A, C–I = 20 μm; B, J = 100 μm.
Fig. 3 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 3. Coecobrya gejianbangi sp. nov. A. Thoracic chaetotaxy. B–D. Abdominal chaetotaxy. B. Abd. I–III. C. Abd. IV. D. Abd. V. Scale bars: 200 μm.
Fig. 9. Clypeal chaetae. A. Diagram. B in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 9. Clypeal chaetae. A. Diagram. B. Coecobrya gejianbangi sp. nov. C. Coecobrya annulata sp. nov. D. Coecobrya ciliata sp. nov. E. Coecobrya brevis. F. Coecobrya pani. Figures of the latter two species after Xu et al. (2012). Scale bars: 40 μm.
Fig. 4 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 4. Coecobrya annulata sp. nov. A. Ant. III organ. B. Dorsal cephalic chaetotaxy. C. Chaetae on the ventral side of head. D. Trochanteral organ, ventral view. E. Hind claw. F. Anterior face and lateral flap of ventral tube. G. Posterior face of ventral tube. H. Mucro. Scale bars: A, C–E, H = 50 μm; B, F–G = 100 μm.
Fig. 2 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 2. Coecobrya gejianbangi sp. nov. A. Ant. III organ. B. Dorsal cephalic chaetotaxy. C. Lateral process of labial palp. D. Chaetae on the ventral side of head. E. Trochanteral organ, ventral view. F. Fore claw. G. Hind claw. H–J. Ventral tube. H. Anterior face. I. Posterior face. J. Lateral flap. K. Manubrial plaque. Scale bars: A, C, E–G, K = 40 μm; B, D, H–J = 100 μm.
FIGURE 5. Steinernema guangdongense n in Steinernema guangdongense sp. n. (Nematoda: Steinernematidae), a new entomopathogenic nematode from southern China with a note on S. serratum (nomen nudum)
FIGURE 5. Steinernema guangdongense n. sp. Lightmicroscope photographs. AB, epiptygma of the first generation females. CD, tails of infective juveniles showing dorsal constriction (arrows), compared to no dorsal constriction in S. longicaudum in EF. G, mature female of the first generation with prominent postanal swelling. H, second generation female with longer tail. Scales: A, B = 18 μm, C = 24 μm, D = 22 μm, E, F = 22 μm.
FIGURE 6 in Steinernema guangdongense sp. n. (Nematoda: Steinernematidae), a new entomopathogenic nematode from southern China with a note on S. serratum (nomen nudum)
FIGURE 6. SEM photographs of Steinernema guangdongense n. sp. infective juvenile. AB, anterior region showing one lateral line, closed mouth (m), amphids (a) and cephalic (c) papillae. C, lateral field with 2 ridges (3 incisures). D, lateral field showing the change of lateral field pattern from 2 to 7 ridges. E, lateral field showing 7 ridges and the middle one (number 4) is divided into 2 making 8 ridges in lateral field. F, lateral field showing phasmid (p) and 7 ridges changing to 4 then 2. Scales: A = 6.67 μm, B = 5 μm, C = 8.60 μm, D F = 6.67 μm.
FIGURES 2A–F. A–B in JIE LIU, SHUQIANG LI & PETER JÄGER (2008) New cave-dwelling huntsman spider species of the genus Sinopoda (Araneae: Sparassidae) from southern China. Zootaxa, 1857, 1-20.
FIGURES 2A–F. A–B. Sinopoda fornicata sp. nov., holotype. C–D. Sinopoda yaojingensis sp. nov., holotype. E–F. Sinopoda crassa sp. nov., holotype. (A, C, E, Epigyne, ventral view; B, D, F, Vulva, dorsal view). Scale lines: 0.2 mm.
The carbon sink potential of southern China after two decades of afforestation
<p>Geological data were provided by China Geological Survey in shapefile with lithology and lithological age in the attribute table. The "class" means the lithology class, where "1" denotes a classification dominated by Dolomite; "2" is a classification dominated by Limestone; "3" represents a classification dominated by Clastic; "4" means water and "5" denotes a classification dominated by Carbonate rocks. "symbol" represents the lithological age.</p> <p>The geomorphological units (Cheng and Zhou, 2014) can be downloaded at the National Tibetan Plateau Third Pole Environment Data Center (https://data.tpdc.ac.cn/en/data/ecb4889a-8d85-4a64-a426-2c74f59fe14f/?q=geomor) in shapefile. It includes 5 types in the attribute table named TypeNames: Flat, Hills, Low relief, Moderate relief, High relief.</p> <p>Hydrological data is available at https://www.webmap.cn/commres.do?method=result25W in shapefile with 3 elements: rivers, lakes, springs and so on. "HYDA" represents the lakes, "HYDL" is rivers, and "HYDP" is springs and wells.</p> <p>Climate data include mean annual precipitation (MAP, mm), mean annual temperature (MAT, °C), aridity index (aridity), humidity index (im), >0°C accumulated temperature (aat0dem, °C-days) and >10°C accumulated temperature (aat10dem, °C-days). MAP and MAT are at a resolution of 1km x 1km from 2000-2015. Aridity index (aridity), humidity index (im), >0°C accumulated temperature (aat0dem, °C-days) and >10°C accumulated temperature (aat10dem, °C-days) are at a resolution of 500m x 500m.</p> <p>Soil properties are also available at the Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences (https://www.resdc.cn/) at a resolution of 1km x 1km. Where names of the soil order codes represent as follows: 10: Alfisols. 11: Semi-alfisol. 13: Xerosol. 15: Primitive soil. 16: Semi-hydric soil. 17: Hydric soil. 18: Saline-alkali soil. 19: Anthrosols. 20: Alpine soil. 21: Ferralsols. 22: Cities. 23: Rocks. 24: Lakes and reservoirs. 25: Rivers. 26: Sand bars and islands in rivers. 27: Glacier and snow cover. 28: Coral reefs and sea islands. 30: Coastal salt farm/aquaculture farm. Soil texture includes clay content (%), silt content (%), and sand content (%).</p> <p>DEM (ASTGTM2_dem) is also available at the Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences (https://www.resdc.cn/) at a resolution of 30m x 30m.</p> <p>This dataset is the percentage of above-ground biomass carbon carrying capacity reached in the eight provinces of southern China and in different forest types from 2002 to 2017 at the resolution of 500m x 500m, with the urban and water areas, cropland, and the southeast margin of the Tibet Plateau masked. The dataset takes values ranging from 0%-100%. 0% represents the highest carbon sequestration potential, while 100% represents carbon sequestration has reached saturation. The dataset can locate areas where vegetation has not yet reached its full potential, which is significant for the implementation and adjustment of ecological engineering. The dataset is publicly available.</p>
Text-fig. 5. Vegetation zones in P. R. China (Editorial Committee of Vegetation Map of China, The Chinese Academy of Sciences 2007), and assumed location of extant reference vegetation type of Wiesa fossil assemblage (rectangle), as revealed from qualitative floristic analysis. Extant reference vegetation type present in southern belt of zone of subtropical evergreen broadleaved forest, with minor overlap into zone of tropical forest. in Assessment Of Phytogeographic Reference Regions For Cenozoic Vegetation: A Case Study On The Miocene Flora Of Wiesa (Germany)
Text-fig. 5. Vegetation zones in P. R. China (Editorial Committee of Vegetation Map of China, The Chinese Academy of Sciences 2007), and assumed location of extant reference vegetation type of Wiesa fossil assemblage (rectangle), as revealed from qualitative floristic analysis. Extant reference vegetation type present in southern belt of zone of subtropical evergreen broadleaved forest, with minor overlap into zone of tropical forest.
Text-fig. 4. Graphical visualization of Phytogeographic Reference Regions Assessment (PRRA) of nearest living relative genera of fossil-taxa from late Early Miocene Wiesa assemblage in eastern Germany. Analysis yields only NLRs which have modern distribution area (partly) in E and SE Asia. For relationships of fossil-taxa to nearest living relatives or ecological equivalents, see Tab. 6; taxa used for analysis marked with asterisks. Three geographic resolutions conducted: a – grid with 1.5° latitude/longitude resolution, b – grid with 2°, c – grid with 3°; similarity column indicates cooccurrences of genera of nearest living relatives in single grid box. Maximum value in our analysis: grid box marked with arrow in map a, located in western Yunnan Province, P. R. China and southern Kachin Province, NE Myanmar (east of Myitkyina city), area with 97.371 7–98.874 2° longitude and 24.586 7–25.837 5° latitude, yields 23 co-occurring species of 13 genera (Tab. 7). in Assessment Of Phytogeographic Reference Regions For Cenozoic Vegetation: A Case Study On The Miocene Flora Of Wiesa (Germany)
Text-fig. 4. Graphical visualization of Phytogeographic Reference Regions Assessment (PRRA) of nearest living relative genera of fossil-taxa from late Early Miocene Wiesa assemblage in eastern Germany. Analysis yields only NLRs which have modern distribution area (partly) in E and SE Asia. For relationships of fossil-taxa to nearest living relatives or ecological equivalents, see Tab. 6; taxa used for analysis marked with asterisks. Three geographic resolutions conducted: a – grid with 1.5° latitude/longitude resolution, b – grid with 2°, c – grid with 3°; similarity column indicates cooccurrences of genera of nearest living relatives in single grid box. Maximum value in our analysis: grid box marked with arrow in map a, located in western Yunnan Province, P. R. China and southern Kachin Province, NE Myanmar (east of Myitkyina city), area with 97.371 7–98.874 2° longitude and 24.586 7–25.837 5° latitude, yields 23 co-occurring species of 13 genera (Tab. 7).
The Meltwater Pulse1A Triggered an Extreme Cooling Event: Evidence From Southern China. Meltwater Pulse Cooling Event (MCE). Winter temperature data during the last deglacial of Huguangyan Maar lake, Surface water temperature and seasonal diatom assemblage data of Huguangyan and Yunlong Lake.
<p>Here we present results of The lake averaged monthly mean surface water temperature over the period from September 2013 to August 2015 from Yunlong Tianchi Lake(YL)(25°52.2′N, 99°16.8′E, altitude: 2551 m a.s.l), southwestern China. The dataset include sediment trap main diatom percentages over the period from September 2013 to August 2015 from YL. Lake water temperature profiles at different depths (1, 3, 6, 9, 11, 13, 16 m) from November 2008 to May 2009 in Huguang Maar Lake (HML)(21°9′N, 110°17′E), Southern China. AMS radiocarbon dates of plant remains and bulk sediment samples for Huguangyan Maar Lake over the last ~17 cal ka BP. The main diatom assemblage percentages (%) from 17 to 10 cal ka BP at Huguangyan Maar Lake. Diatom-based reconstruction of winter temperature (WT) from 17 to 10 cal ka BP at Huguangyan Maar Lake.</p>
Figure 3 in Characterization of root-knot nematodes infecting mulberry in Southern China
Figure 3: Phylogenetic relationships within root-knot nematodes on mulberry as inferred from Bayesian analysis of the D2-D3 region of the 28S gene sequences. Posterior probability values more than 70% are given on appropriate clades.
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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.