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122 results for “Shandong”
Subspecies and Distribution. L.t.tolaiPallas,1778—InnerMongolia(=NeiMongol),andGansu(NCChina). L.t.buchariensisOgnev,1922—TajikistanandNEAfghanistan. L.t.cheybaniBaloutch,1978—SWIran(ZagrosMts). L.t.cinnamomeusShamel,1940—SWSichuan,andNYunnan(SCChina). L.t.filchneriMatschie,1908—Shaanxi(CChina). L.t.lehmanniSevertzov,1873—SKazakhstan,Turkmenistan,andextremeN&NEIran,EtoSSiberia,Mongolia,andXinjiang(NWChina). L. t. swinhoei Thomas, 1894 — from Heilongjiang, Jilin, Liaoning, Inner Mongolia S to Hebei, Beijing, Henan, Shaanxi, Shanxi, and Shandong (NE & E China). The Tolai Hare occurs in the steppes E of the Caspian Sea, S to NE & SW Iran, E through the Middle Asian republics to Afghanistan, and from Kazakhstan and S Siberia to Mongolia, S Russian Far East, NW, C & NE China; an isolated population lives in S Iraq and SW Iran. A single specimen in South Asia might extend the distribution of the Tolai Hare as far S as Jammu and Kashmir, N India. in Leporidae
Subspecies and Distribution. L.t.tolaiPallas,1778—InnerMongolia(=NeiMongol),andGansu(NCChina). L.t.buchariensisOgnev,1922—TajikistanandNEAfghanistan. L.t.cheybaniBaloutch,1978—SWIran(ZagrosMts). L.t.cinnamomeusShamel,1940—SWSichuan,andNYunnan(SCChina). L.t.filchneriMatschie,1908—Shaanxi(CChina). L.t.lehmanniSevertzov,1873—SKazakhstan,Turkmenistan,andextremeN&NEIran,EtoSSiberia,Mongolia,andXinjiang(NWChina). L. t. swinhoei Thomas, 1894 — from Heilongjiang, Jilin, Liaoning, Inner Mongolia S to Hebei, Beijing, Henan, Shaanxi, Shanxi, and Shandong (NE & E China). The Tolai Hare occurs in the steppes E of the Caspian Sea, S to NE & SW Iran, E through the Middle Asian republics to Afghanistan, and from Kazakhstan and S Siberia to Mongolia, S Russian Far East, NW, C & NE China; an isolated population lives in S Iraq and SW Iran. A single specimen in South Asia might extend the distribution of the Tolai Hare as far S as Jammu and Kashmir, N India.
Distribution. NE & C China (Inner Mongolia [= Nei Mongol], Heilongjiang, Gansu, Ningxia, Shaanxi, Shanxi, Hebei, Beijing, Liaoning, Henan, Shandong, and Jiangsu); probably Mongolia. in Talpidae
Distribution. NE & C China (Inner Mongolia [= Nei Mongol], Heilongjiang, Gansu, Ningxia, Shaanxi, Shanxi, Hebei, Beijing, Liaoning, Henan, Shandong, and Jiangsu); probably Mongolia.
Subspecies and Distribution. L.m.mandarinusMilne-Edwards,1871—NC&ECChina(SInnerMongolia[=NeiMongol],Shaanxi,Shanxi,Henan,andNEAnhui). L.m.faeceusG.M.Allen,1924—EChina(SEInnerMongolia,Hebei,WLiaoning,Beijing,Shandong,andJiangsu). L.m.johannesThomas,1910—NCChina(NEShanxi). L.m.kishida:Mori,1930—KoreanPeninsula. L. m. vinogradovi Fetisov, 1936 — S Transbaikalia in Russia (S Buryatia) and NC Mongolia. Also present in NE Inner Mongolia, but subspecies involved not known. in Cricetidae
Subspecies and Distribution. L.m.mandarinusMilne-Edwards,1871—NC&ECChina(SInnerMongolia[=NeiMongol],Shaanxi,Shanxi,Henan,andNEAnhui). L.m.faeceusG.M.Allen,1924—EChina(SEInnerMongolia,Hebei,WLiaoning,Beijing,Shandong,andJiangsu). L.m.johannesThomas,1910—NCChina(NEShanxi). L.m.kishida:Mori,1930—KoreanPeninsula. L. m. vinogradovi Fetisov, 1936 — S Transbaikalia in Russia (S Buryatia) and NC Mongolia. Also present in NE Inner Mongolia, but subspecies involved not known.
FIGURE 2 in Coniella castanea sp. nov. on Castanea mollissima from Shandong Province, China
FIGURE 2. Coniella castanea (SAUCC 200313). a Leaves of host plant. b Surface view of colony after 7 days on PDA. c Reverse view of colony after 7 days on PDA. d Conidiomata sporulating on PDA. e–k Conidiogenous cells with developing Conidia. l Conidia. Scale bars: e–l= 10 μm.
FIGURE 1 in Coniella castanea sp. nov. on Castanea mollissima from Shandong Province, China
FIGURE 1. Phylogram of Coniella based on combined ITS, LSU, RPB2 and TEF1-α genes. The ML and BI bootstrap support values above 70 % and 0.90 BYPP are shown at the first and second position above nodes. Strains from the current study are in red. Tree is rooted with [out group]. Some branches were shortened to fit them to the page – these are indicated by two diagonal lines with the number of times a branch was shortened indicated next to the lines.
The dataset of "Characteristics of Urban Interaction Network in Shandong Province from the Perspective of Traffic Flow and Information Flow"
<p>There are the datasets of the research named "Characteristics of Urban Interaction Network in Shandong Province from the Perspective of Traffic Flow and Information Flow".</p>
FIGURES 1–9. FIGURES 1–5 in A new species of the genus Xya Latreille, 1809 from Shandong, China (Orthoptra, Tridctyloidea, Tridactylidae)
FIGURES 1–9. FIGURES 1–5. Xya shandongensis sp. nov. 1. body in lateral view Ƌ; 2. end of abdomen in dorsal view ♁; 3. head pronotum in lateral view ♁; 4. head in frontal view ♀; 5. body in dorsal view ♀; 6. end of abdomen in ventral view ♀; FIGURES 7– 9. Xya japonica (Haan, 1842) 7. head in frontal view ♀; 8. epiproct in dorsal view ♁; 9. body in dorsal view ♀. (figs. 7–9 after Murai, 2005).
FIGURE 10 in A new species of the genus Xya Latreille, 1809 from Shandong, China (Orthoptra, Tridctyloidea, Tridactylidae)
FIGURE 10. Landscape habitat of Xya shandongensis sp. nov. (China, Shandong, Junan county, Panlong Lake, 35°12′ 29"N, 118°51′23"E, alt. 106m.).
FIGURES 36–40 in A new freshwater species Achnanthes licunese sp. nov. (Achnanthaceae, Bacillariophyta) from pebbles of Licun River, Shandong Province, China
FIGURES 36–40. Achnanthes licunese sp. nov. SEM, the internal view of araphid valve (ARV). 36. internal view of the whole valve. 37. central area of ARV. 38. detailed internal view of virgae and areolae 39–40. apices of ARV. Scale bars: 10 µm (36); 2 µm (37); 1 µm (38–40).
FIGURES 21–23 in A new freshwater species Achnanthes licunese sp. nov. (Achnanthaceae, Bacillariophyta) from pebbles of Licun River, Shandong Province, China
FIGURES 21–23. Achnanthes licunese sp. nov. SEM, girdle view. 21. a complete girdle view of the frustule and the cone-shaped spines (arrows). 22–23. middle detail of 21, showing the areolae and silica granules on the girdle bands (wavy arrows). Scale bar: 10 µm (21); 2 µm (22–23).
FIGURES 28–31 in A new freshwater species Achnanthes licunese sp. nov. (Achnanthaceae, Bacillariophyta) from pebbles of Licun River, Shandong Province, China
FIGURES 28–31. Achnanthes licunese sp. nov. SEM, the internal view of raphid valve (RV). 28. internal view of the whole valve. 29. central area of the valve, showing the proximal raphe ends, and central raphe endings are hookshaped. 30. detail of the internal areolae, showing the areolae is not occluded by the complex cribra. 31. apices of the valve, showing the detail view of areolae (arrows), terminal raphe fissure, helictoglossae, and margin of valve. Scale bars: 10 µm (28); 2 µm (29); 1 µm (31); 0.5 µm (30).
FIGURES 24–27 in A new freshwater species Achnanthes licunese sp. nov. (Achnanthaceae, Bacillariophyta) from pebbles of Licun River, Shandong Province, China
FIGURES 24–27 Achnanthes licunese sp. nov. SEM, the external view of raphid valve (RV). 24. external view of the whole valve. 26. central area of RV, showing the proximal raphe ends. 25, 27. apices of the valve, showing the terminal raphe fissure and areolae. Scale bars: 10 µm (24); 2 µm (26); 1 µm (25, 27).
FIGURES 32–35 in A new freshwater species Achnanthes licunese sp. nov. (Achnanthaceae, Bacillariophyta) from pebbles of Licun River, Shandong Province, China
FIGURES 32–35. Achnanthes licunese sp. nov. SEM, the external view of araphid valve (ARV). 32. external view of the whole valve. 34. central area of ARV. 33, 35. details of the apices of the valve, showing areolae and spines on the valve. Scale bars: 10 µm (32); 2 µm (34); 1 µm (33, 35).
FIGURES 3–20 in A new freshwater species Achnanthes licunese sp. nov. (Achnanthaceae, Bacillariophyta) from pebbles of Licun River, Shandong Province, China
FIGURES 3–20. Achnanthes licunese sp. nov. LM. 3–8. frustule in girdle view. 9–14. size diminution series of raphe valve. 15–20. size diminution series of rapheless valve. Scale bar: 10 μm.
FIGURES 1–2 in A new freshwater species Achnanthes licunese sp. nov. (Achnanthaceae, Bacillariophyta) from pebbles of Licun River, Shandong Province, China
FIGURES 1–2. Achnanthes licunses sp. nov. LM, the live cells 1. An unprocessed cell in girdle view. 2. Two unprocessed cells in girdle view. Scale bar: 10 μm.
TABLE 1 in A new freshwater species Achnanthes licunese sp. nov. (Achnanthaceae, Bacillariophyta) from pebbles of Licun River, Shandong Province, China
<p><b>TABLE 1.</b> Comparison of morphological characteristics of <i>Acnanthes licunese sp.nov.</i> and closely related taxa.</p><table><tbody><tr><th>Species/feature</th><th>Dimension Length(µm)</th><th>Width(µm)</th><th>Valve outline</th><th>center</th><th>Apices</th><th>Striae in 10 µm on RV</th><th>Striae in 10 µm on ARV</th><th>Spines</th><th>Marginal ridge</th><th>Terminal orbiculi on ARV</th><th>Habitat</th><th>Sources</th></tr></tbody><tbody><tr><th><i>A. licunese sp.nov.</i></th><td>38.0–53.5</td><td>10.0–12.5</td><td>linear to linear-lanceolate</td><td>slightly constricted</td><td>obtuse</td><td>9–10</td><td>9–10</td><td>cone-shaped, distributed along the margin on the ARV</td><td>absent</td><td>absent</td><td>Freshwater</td><td>This study</td></tr><tr><th><i>A. secretitaeniata</i> K.Toyoda & Ji. Tanaka</th><td>18.0–67.0</td><td>9.0–13.0</td><td>lanceolate to linear-lanceolate</td><td>slightly constricted</td><td>broadly rounded</td><td>9–11</td><td>8–10</td><td>plate-like, at each apex</td><td>present</td><td>absent</td><td>Brackish water</td><td>Heudre <i>et al.</i>, 2020</td></tr><tr><th><i>A. sinaensis</i> (Hustedt) Levkov, Tofilovska & Wetzel</th><td>32.5–43.0</td><td>8.5–11.5</td><td>linear to linear-lanceolate</td><td>slightly broad</td><td>broadly rounded to trunctate</td><td>10–11</td><td>10–11</td><td>absent</td><td>present</td><td>present</td><td>Freshwater</td><td>Tofilovska <i>et al.</i>, 2014</td></tr><tr><th><i>A. prominula</i> Levkov & Tofilovska</th><td>18.5–43.0</td><td>8.5–10.5</td><td>linear-lanceolate or elliptic-lanceolate</td><td>slightly broad</td><td>attenuated and narrowly rounded</td><td>11–12</td><td>10–12</td><td>absent</td><td>present</td><td>present</td><td>Freshwater</td><td>Tofilovska <i>et al.</i>, 2014</td></tr><tr><th><i>A</i>. <i>coarctata</i> (Brébisson & Smith) Grunow</th><td>29.0–44.5</td><td>7.0–9.5</td><td>biundulate</td><td>constricted</td><td>attenuated and narrowly rounded or rostrate and rounded</td><td>12–14</td><td>12–14</td><td>absent</td><td>present</td><td>present</td><td>Freshwater</td><td>Tofilovska <i>et al.</i>, 2014</td></tr></tbody></table>
Figure 2 in Effects of fragmentation on genetic variation in populations of the terrestrial earthworm Drawida japonica Michaelsen, 1892 (Oligochaeta, Moniligastridae) in Shandong and Liaodong peninsulas, China
Figure 2. Maximum-parsimony (MP) tree of the unique haplotypes. Numbers at nodes represent bootstrap values (> 50) as a measure of support.
Figure 4 in Effects of fragmentation on genetic variation in populations of the terrestrial earthworm Drawida japonica Michaelsen, 1892 (Oligochaeta, Moniligastridae) in Shandong and Liaodong peninsulas, China
Figure 4. Mismatch curve of nucleotide pairwise based on 16S sequences. Exp, expected value; Obs, observed value.
Figure 3 in Effects of fragmentation on genetic variation in populations of the terrestrial earthworm Drawida japonica Michaelsen, 1892 (Oligochaeta, Moniligastridae) in Shandong and Liaodong peninsulas, China
Figure 3. Maximum-likelihood (ML) tree of the unique haplotypes. Bootstrap values (> 50) are shown on the nodes; Bayesian inference (BI) tree based on the analysis of the unique haplotypes. Posterior probability values (> 0.5) are shown.
Figure 5 in Effects of fragmentation on genetic variation in populations of the terrestrial earthworm Drawida japonica Michaelsen, 1892 (Oligochaeta, Moniligastridae) in Shandong and Liaodong peninsulas, China
Figure 5. Mismatch curve of nucleotide pairwise based on 28S sequences. Exp, expected value; Obs, observed value.
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Allen Brain Atlas
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International Brain Laboratory public data
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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.