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214 results for “Mountain areas”
FIGURE. Collection areas in northeastern China. A. Changchun area in Jilin Province. B. Jilin area in Jilin Province. C. Mountanious area in southern Heilongjiang Province. D. Area around Changbai Mountains. E. Baicheng area in western Jilin Province. F. Yanbian area in eastern Jilin Province. G. Tonghua area in southeastern Jilin Province. in Phylogenetic approach for identification and life cycles of Puccinia (Pucciniaceae) species on Poaceae from northeastern China
FIGURE. Collection areas in northeastern China. A. Changchun area in Jilin Province. B. Jilin area in Jilin Province. C. Mountanious area in southern Heilongjiang Province. D. Area around Changbai Mountains. E. Baicheng area in western Jilin Province. F. Yanbian area in eastern Jilin Province. G. Tonghua area in southeastern Jilin Province.
Water uptake strategies by typical broadleaf and coniferous trees in the Loess Plateau mountain area of northern China
<p class="1">Poor precipitation in the Loess Plateau area may significantly influence water uptake strategies of the plants growing there. The water sources of these trees have not been studied to date. We investigated the impacts of precipitation (before and after) on water uptake strategies of typical broadleaf and coniferous trees in the Loess Plateau mountain area of northern China by using hydrogen and oxygen stable isotope techniques. Our results indicated that water sources of these two tree types varied before and after rainfall. <i>Robinia pseudoacacia</i>, a broadleaf tree, absorbed water majorly from the 30–40 cm (57.8%) soil layer before precipitation and from the 20–30 cm (58.5%) soil layer after precipitation. However, <i>Pinus tabuliformis</i>, a coniferous tree, mainly absorbed water from 20–30 cm (24.9%) and 10–20 cm (21.6%) soil layers before precipitation and from 0–10 cm (39.8%) and 10–20 cm (44%) soil layers after precipitation. Moreover, the herbaceous of broadleaf plant has higher complexity of the community through filed investigation. Thus, <i>R. pseudoacacia</i> and <i>P. tabuliformis</i> exhibited peculiar difference in terms of water uptake, indicating that they are suitable to grow together as forest vegetation in arid and semi-arid areas. Overall, our results provided vital information for sustainable afforestation management in the Loess Plateau mountain area of northern China.</p>
Distribution. Endemic to the mountains of E Nigeria and the Adamawa Massif and surrounding areas in W Cameroon. in Bovidae
Distribution. Endemic to the mountains of E Nigeria and the Adamawa Massif and surrounding areas in W Cameroon.
Distribution. Two disjunct areas across the lowland rainforest belt of W Africa (Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Togo & Benin) and C Africa through the Congo Basin (Cameroon, Gabon, Republic of the Congo, DR Congo, Central African Republic & extreme SW Sudan), and five very small disjunct populations in mountainous areas in C Kenya. in Bovidae
Distribution. Two disjunct areas across the lowland rainforest belt of W Africa (Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Togo & Benin) and C Africa through the Congo Basin (Cameroon, Gabon, Republic of the Congo, DR Congo, Central African Republic & extreme SW Sudan), and five very small disjunct populations in mountainous areas in C Kenya.
Distribution. Malay Peninsula in S Thailand (only in a small area on the border with Malaysia), NW & C Peninsular Malaysia (largely restricted to mountainous areas in the W of the country, S of the Perak River and N of the Muar River, and Tasek Bera across to the Pahang River), and W Sumatra where confined to the Barisan Mts; it may have formerly occurred on Bangka I. in Hylobatidae
Distribution. Malay Peninsula in S Thailand (only in a small area on the border with Malaysia), NW & C Peninsular Malaysia (largely restricted to mountainous areas in the W of the country, S of the Perak River and N of the Muar River, and Tasek Bera across to the Pahang River), and W Sumatra where confined to the Barisan Mts; it may have formerly occurred on Bangka I.
Distribution. Endemic to C & SE Sulawesi; known from various lowland and more mountainous regions, including Mt Rorekatimbo, Mt Gandangdewata, Mt Balease, and Mt Nokilalaki. Together with the Elongated White-toothed Shrew (C. elongata) this is the only wild shrew occurring on the SE peninsula, but lack of adequate sampling in most pristine areas of S Sulawesi hinders precise biogeographical inferences. in Soricidae
Distribution. Endemic to C & SE Sulawesi; known from various lowland and more mountainous regions, including Mt Rorekatimbo, Mt Gandangdewata, Mt Balease, and Mt Nokilalaki. Together with the Elongated White-toothed Shrew (C. elongata) this is the only wild shrew occurring on the SE peninsula, but lack of adequate sampling in most pristine areas of S Sulawesi hinders precise biogeographical inferences.
Distribution. Mountainous areas in Morocco (Rif, High and Middle Atlas) and Algeria (Grande and Petite Kabylie); historically it also occurred in W Tunisia but is now extinct there. A free-ranging population occurs in Gibraltar introduced there by the British in 1740. in Cercopithecidae
Distribution. Mountainous areas in Morocco (Rif, High and Middle Atlas) and Algeria (Grande and Petite Kabylie); historically it also occurred in W Tunisia but is now extinct there. A free-ranging population occurs in Gibraltar introduced there by the British in 1740.
Distribution. Found in a small area of mountainous terrain in Western Highlands and Chimbu provinces, Papua New Guinea, with records from slopes of the Hagen Range, Mt Giluwe, and Mt Wilhelm. in Muridae
Distribution. Found in a small area of mountainous terrain in Western Highlands and Chimbu provinces, Papua New Guinea, with records from slopes of the Hagen Range, Mt Giluwe, and Mt Wilhelm.
Distribution. Throughout various mountainous areas of New Guinea, Yapen I, New Britain I, and extreme NE Australia (NE Queensland: Iron Range, and from Shiptons Flat to Koombooloomba). in Muridae
Distribution. Throughout various mountainous areas of New Guinea, Yapen I, New Britain I, and extreme NE Australia (NE Queensland: Iron Range, and from Shiptons Flat to Koombooloomba).
Distribution. Currently recorded only on N ridge of Mt Halcon, Mindoro I, Philippines; likely widespread in mountains of Mindoro, an area that remains poorly surveyed for small mammals. in Muridae
Distribution. Currently recorded only on N ridge of Mt Halcon, Mindoro I, Philippines; likely widespread in mountains of Mindoro, an area that remains poorly surveyed for small mammals.
Vineyard and Apple Orchard Suitability Maps for Mountainous Areas (Southern Pyrenees and Pre-Pyrenees)
<p>The manuscript related to this dataset can be consulted trought:</p> <p>The layers available in this dataset are in EPSG: WGS84.</p> <ul> <li><strong>Indicators</strong> <ul> <li><strong>BBL.tif </strong>- Hydrothermic index of Branas, Bernon, Levadoux (ºC*mm)</li> <li><strong>CDls.tif </strong>- Cold Days late spring (days)</li> <li><strong>FRea.tif </strong>- Frost Risk early autumn (days)</li> <li><strong>FRls_vineyard.tif </strong>- Frost Risk late spring vineyard (days)</li> <li><strong>FRls_apple.tif </strong>- Frost Risk late spring apple orchard (days)</li> <li><strong>GDD.tif</strong> - Growing Degree Days (ºC)</li> <li><strong>GSP.tif </strong>- Growing Season Precipitation (mm)</li> <li><strong>GST.tif </strong>- Growing Season Temperature (ºC)</li> <li><strong>Ha</strong><strong>.tif </strong>- Hail (days)</li> <li><strong>HI</strong><strong>.tif </strong>- Heliothermal Index of Huglin (ºC)</li> <li><strong>NCIr</strong><strong>.tif </strong>- Night Cool Index ripenning (ºC)</li> <li><strong>NHN.tif</strong> - Need Hydric Needs (mm/year)</li> <li><strong>SHDr.tif </strong>- Stressful Hot Days ripening (days)</li> <li><strong>WI.tif </strong>- Winkler Index (ºC)</li> <li><strong>CaCO3.tif </strong>- Calcium Carbonates (%)</li> <li><strong>CEC.tif </strong>- Cation Exchange Capacity (cmol/kg)</li> <li><strong>pH.tif </strong>- pH</li> <li><strong>SD.tif </strong>- Soil Depth (cm)</li> <li><strong>TAW.tif</strong> - Total Available Water (mm)</li> <li><strong>Te.tif</strong> - Texture</li> <li><strong>TOC.tif </strong>- Topsoil Organic Carbon (%)</li> <li><strong>As.tif </strong>- Aspect</li> <li><strong>GSR.tif </strong>- Growing season Solar Radiation (kWh/m2)</li> <li><strong>Sl.tif </strong>- Slope (%)</li> </ul> </li> </ul> <ul> <li><strong>Indicators_Suitability</strong> <ul> <li><strong>BBL_suitability.tif </strong>- Hydrothermic index of Branas, Bernon, Levadoux (ºC*mm)</li> <li><strong>CDls_suitability.tif </strong>- Cold Days late spring (days)</li> <li><strong>FRea_suitability.tif </strong>- Frost Risk early autumn (days)</li> <li><strong>FRls_vineyard_suitability.tif </strong>- Frost Risk late spring vineyard (days)</li> <li><strong>FRls_apple_suitability.tif </strong>- Frost Risk late spring apple orchard (days)</li> <li><strong>GDD_suitability.tif</strong> - Growing Degree Days (ºC)</li> <li><strong>GSP_suitability.tif </strong>- Growing Season Precipitation (mm)</li> <li><strong>GST_suitability.tif </strong>- Growing Season Temperature (ºC)</li> <li><strong>Ha_suitability</strong><strong>.tif </strong>- Hail (days)</li> <li><strong>HI_suitability</strong><strong>.tif </strong>- Heliothermal Index of Huglin (ºC)</li> <li><strong>NCIr_suitability</strong><strong>.tif </strong>- Night Cool Index ripenning (ºC)</li> <li><strong>NHN_suitability.tif</strong> - Need Hydric Needs (mm/year)</li> <li><strong>SHDr_suitability.tif </strong>- Stressful Hot Days ripening (days)</li> <li><strong>WI_suitabilitytif</strong> - Winkler Index (ºC)</li> <li><strong>CaCO3_suitability.tif </strong>- Calcium Carbonates (%)</li> <li><strong>CEC_suitability.tif </strong>- Cation Exchange Capacity (cmol/kg)</li> <li><strong>pH_suitability.tif </strong>- pH</li> <li><strong>SD_suitability.tif </strong>- Soil Depth (cm)</li> <li><strong>TAW_suitability.tif</strong> - Total Available Water (mm)</li> <li><strong>Te_suitability.tif</strong> - Texture</li> <li><strong>TOC_suitability.tif </strong>- Topsoil Organic Carbon (%)</li> <li><strong>As_suitability.tif </strong>- Aspect</li> <li><strong>GSR_suitability.tif </strong>- Growing season Solar Radiation (kWh/m2)</li> <li><strong>Sl_suitability.tif </strong>- Slope (%)</li> </ul> </li> </ul> <ul> <li><strong>Suitability</strong> <ul> <li><strong>Vineyard_suitability.tif </strong>- Vineyard Suitability map (Minumum Suitability 0 - 100 Maximum Suitability)</li> <li><strong>Apple_orchard_suitability.tif </strong>- Apple Orchard Suitability map (Minumum Suitability 0 - 100 Maximum Suitability) </li> </ul> </li> </ul>
Air temperature measurements using autonomous self-recording dataloggers in mountainous and snow covered areas
<p>Data and sctripts employed on submitted article on Water Resources Research (AGU Journal)</p>
FIGURES 34–41 in Achnanthidium sinense sp. nov. (Bacillariophyta) from the Wuling Mountains Area, China
FIGURES 34–41. Achnanthidium sinense, sp. nov., SEM. 34–41. External views of middle part of raphe valve, note the stria variation around the central area. 38–41. External views of middle part of rapheless valve, note the stria variation around the central area. Scale bars = 5 μm.
FIGURES 30–33 in Achnanthidium sinense sp. nov. (Bacillariophyta) from the Wuling Mountains Area, China
FIGURES 30–33. Achnanthidium sinense, sp. nov., SEM. 30. External view of rapheless valve, note the slightly radiate striae throughout the valve. 31. Internal view of rapheless valve, note the slightly radiate striae throughout the valve. 32–33. Girdle views. 32. Proliferating cells, note the notches on the mantles. 33. A frustule with convex rapheless valve discernible. Scale bars = 10 μm.
FIGURES 2–21 in Achnanthidium sinense sp. nov. (Bacillariophyta) from the Wuling Mountains Area, China
FIGURES 2–21. Achnanthidium sinense, sp. nov., LM. 2–11. Ten raphe valves showing size reduction, note the lanceolate valve outline and distinct proximal raphe ends. 12–20. Nine rapheless valves showing size reduction, note the lanceolate valve outline. 2 and 12. Photographs of isotype specimens. 11 and 14. Photographs of holotype specimens. 21. Girdle view, note the shallow v-shaped outline. Scale bar (in Fig. 2) = 10 μm for all figures.
FIGURES 22–29 in Achnanthidium sinense sp. nov. (Bacillariophyta) from the Wuling Mountains Area, China
FIGURES 22–29. Achnanthidium sinense, sp. nov., raphe valves, SEM. 22. External view of raphe valve, note the narrow lanceolate axial area. 23. Internal view of raphe valve, note the narrow lanceolate axial area. 24–26. Details of Fig. 22, note the hooked terminal raphe fissures and parallel or slightly convergent striae at the apices. 27–29. Details of Fig. 23, note the parallel or slightly convergent striae at the apices, and curved proximal raphe endings. Scale bars = 5 μm.
FIGURES 47–50 in Adlafia sinensis sp. nov. (Bacillariophyceae) from the Wuling Mountains Area, China, with reference to the structure of its girdle bands
FIGURES 47–50. Adlafia sinensis sp. nov., SEM. 47. A dismembered frustule, showing the valvocopula with one row of areola on both the pars interior and pars exterior (arrow), and c. five striae located only on the mantle (arrows). 48–50. Girdle view showing five striae located only on the mantle (arrows). Scale bars = 5 μm.
FIGURES 43–46 in Adlafia sinensis sp. nov. (Bacillariophyceae) from the Wuling Mountains Area, China, with reference to the structure of its girdle bands
FIGURES 43–46. Adlafia sinensis sp. nov., SEM. 43. Detail of Fig. 41, showing the hooked terminal raphe fissures continuing onto the mantle, open girdle band (arrow), and two rows of poroids become only one row distal the raphe fissure (curved arrow). 44. Detail of Fig. 40, showing the structure of the cingulum at the apex, note the valvocopulae (VC), two segmental bands (B2 and B3), and distinct gap. 45. Detail of Fig. 40, showing the deep mantle and the valvocopula connecting epivalve with the hypovalve. 46. Detail of Fig. 40, showing the structure of the cingulum at the apex, note the valvocopulae (VC), and distinct gap. Scale bars = 1 μm.
FIGURES 40–42 in Adlafia sinensis sp. nov. (Bacillariophyceae) from the Wuling Mountains Area, China, with reference to the structure of its girdle bands
FIGURES 40–42. Adlafia sinensis sp. nov., SEM. 40–42. Three types of frustules. 40. One very slightly dismembered frustule, showing the epivalve (EV), hypovalve (HV) and valvocopula (VC). 41. One slightly dismembered frustule, showing the epivalve (EV), hypovalve (HV) and valvocopula (VC). Note the deep mantle, striae continuing onto the mantle, but seven striae located only on the mantle (arrowheads). 42. One dismembered frustule or a released frustule after new sibling valve formation, note the hypovalve (HV), the epivalve (EV), and the valvocopula (VC). Scale bars = 5 μm.
FIGURES 2–35 in Adlafia sinensis sp. nov. (Bacillariophyceae) from the Wuling Mountains Area, China, with reference to the structure of its girdle bands
FIGURES 2–35. Adlafia sinensis sp. nov., LM. 2–35. 34 valves showing the variation in valve outline, note the central raphe endings discernible only in some specimens. 29. Photograph of holotype. Scale bar (in Fig. 1) =10 μm for all figures.
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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.
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DANDI Archive for NWB datasets
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