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656 results for “Northern China”
Phlorest phylogeny derived from Zhang et al 2019 'Phylogenetic evidence for Sino-Tibetan origin in northern China in the Late Neolithic'
<p>Cite the source of the dataset as:</p> <blockquote> <p>Zhang M, Yan S, Pan W, & Jin L. 2019. Phylogenetic evidence for Sino-Tibetan origin in northern China in the Late Neolithic. Nature, 569, 112–115.</p> </blockquote>
Savanna-like Mammalian Community in the Mid-Miocene of Northern China--Supplementary Data
<p><strong><span>Supplementary Data 1:</span></strong><span> Stable Carbon and Oxygen isotopes data of Junggar Basin and Tongxin region, China.</span></p> <p><strong><span>Supplementary Data 2:</span></strong><span> Teeth hypsodonty of herbivorous mammals from China and Europe, including Sandelzhausen, Steinheim, Sansan, Madrid Basin, Qaidam Basin, Tunggur region, Baode, Lantian, Junggar Basin and Tongxin region.</span></p> <p><strong><span>Supplementary Data 3: </span></strong><span>Body mass of herbivorous mammals from different locations in China. </span></p>
Characteristic and spatiotemporal variation of air pollution in Northern China based on correlation analysis and clustering analysis of five air pollutants
<p>original daily data for 'Characteristic and spatiotemporal variation of air pollution in Northern China based on correlation analysis and clustering analysis of five air pollutants'</p>
Figure 10 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 10. Species ranges, phyletic relationship, and zoogeographical positions of the Paradicrocerus–Stephanocemas clade. Most of the species ranges are approximate. Phyletic relationship is based on one of the shortest trees in our cladistic analysis, and some indeterminate taxa not included in the cladogram are inserted here based on our estimates of their relationships. The antlers are scaled to their approximate relative size, and dashed lines are mostly our own reconstructions of missing tines.
Figure 9 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 9. Strict consensus of four shortest trees (tree length = 12) of the Paradicrocerus–Stephanocemas clade found by the branch and bound option of the PAUP program on a ten taxa ¥ nine characters data matrix (Table 1).
Figure 8. IVPP V15726 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 8. IVPP V15726, Stephanocemas sp. from IVPP locality CD0406. A, dorsal, and B, ventral views of antler fragment. Scale is for both views.
Figure 6. IVPP V15724 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 6. IVPP V15724, referred specimen of Stephanocemas palmatus sp. nov. A, dorsal, B, ventral, and C, medial views of posterior palm portion of a juvenile antler.
Figure 7. IVPP V15725 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 7. IVPP V15725, Stephanocemas sp. from IVPP locality CD9818. A, stereophoto of dorsal view, B, lateral view, and C, ventral view of partial antler.
Figure 5. IVPP V15723 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 5. IVPP V15723, referred specimen of Stephanocemas palmatus sp. nov. A, dorsal, and B, ventral views of palm portion of antler.
Figure 4. IVPP V15722 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 4. IVPP V15722, left antler without pedicel, holotype of Stephanocemas palmatus sp. nov. from Qaidam Basin, northern Tibetan Plateau. A, medial, and B, ventral views. Left is posterior and right is anterior.
Figure 3 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 3. Stereophoto of dorsal view of IVPP V15722, left antler without pedicel, holotype of Stephanocemas palmatus sp. nov. from Qaidam Basin, northern Tibetan Plateau. Top is posterior and bottom is anterior.
Figure 2 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 2. Satellite image of the Barun Yawula anticline, with key fossil localities and their relative stratigraphical positions indicated. The east–west trending fold is asymmetrical with the south limb dipping more steeply than the north limb. A prominent resistant bed (a dark–light band combination, indicated by black dashed lines) within the rusty green sandstones layers helps to trace stratigraphical relationships between localities in eastern and western ends of the anticline, although multiple faults (with offsets ranging from 50 to 500 m), particularly those in the eastern end, complicate correlations. White lines are the measured section.
Fig. 5 in Eucricetodon (Rodentia, Mammalia) from the Late Oligocene of the Junggar basin, northern Xinjiang, China
Fig. 5. Mandible of Eucricetodon aff. E. caducus, labial view, from the late Oligocene of the Junggar basin, locality XJ 99006 (V15974.14).
Fig. 1 in Eucricetodon (Rodentia, Mammalia) from the Late Oligocene of the Junggar basin, northern Xinjiang, China
Fig. 1. Terminology used in this paper to described molars, modified from Hugueney (1999) for the first molars and from Freudenthal and Daams (1988) for third molars. (A) Upper molars, M1, M2 and M3: 1. anterior crest; 2. anterocone; 3. labial anteroloph; 4. protocone spur 5. paracone; 6. paracone spur; 7. mesosinus; 8. mesostyle; 9. mesoloph; 10. metalophule; 11. metacone; 12. posterosinus; 13. posteroloph; 14. entoloph; 15. hypocone; 16. sinus; 17. lingual cingulum; 18. 2nd mesoloph; 19. protolophule; 20. protocone; 21. protocone platform; 22. protostyle spur; 23. protostyle; 24. lingual anteroloph; 25. protosinus; 26. anterosinus; 27. protolophule spur; 28. entomesoloph; 29. anterolophule; 30. neomesoloph; 31. neometalophule; (B) Lower molars, m1, m2 and m3: 1. lingual anterolophid; 2. metaconid; 3. metaconid ridge; 4. protoconid hind arm; 5. mesostylid; 6. mesolophid; 7. entoconid; 8. hypolophulid; 9. posterolophid; 10. posterosinusid; 11. hypoconid hind arm; 12. ectolophid; 13. hypoconid; 14. ectomesolophid; 15. sinusoid; 16. ectostylid; 17. mesoconid; 18. 2nd mesolophid; 19. protoconid; 20. protosinusid; 21. labial anterolophid; 22. anterolophulid; 23. metalophulid; 24. anteroconid; 25. metaconid spur; 26. mesosinusid; 27. lingual cingulum; 28. labial posterolophid; 29. labial cingulum; 30. anterosinusid; 31. metalophulid spur.
Fig. 4. Eucricetodon aff. E in Eucricetodon (Rodentia, Mammalia) from the Late Oligocene of the Junggar basin, northern Xinjiang, China
Fig. 4. Eucricetodon aff. E. caducus from the late Oligocene of the Junggar basin. A–C. lower incisor and molars from XJ 20003 (V15975.1–3). D–F. molars from XJ 200208 (V15976.1–3). G–O. molars from XJ 200209 (V15977.1–9).
Fig. 3. Eucricetodon aff. E in Eucricetodon (Rodentia, Mammalia) from the Late Oligocene of the Junggar basin, northern Xinjiang, China
Fig. 3. Eucricetodon aff. E. caducus from the late Oligocene of the Junggar basin, locality XJ 99006. A–J. upper molars (V15974.1–10). K–S. lower molars (V15974.11–19).
Fig. 2. Eucricetodon aff. E in Eucricetodon (Rodentia, Mammalia) from the Late Oligocene of the Junggar basin, northern Xinjiang, China
Fig. 2. Eucricetodon aff. E. caducus from the late Oligocene of the Junggar basin, locality XJ 98024. A–I. upper molars (V159873.1–9). J–O. lower molars (V159873.10–15). P–Q. lower incisors (V159873.16–17).
Three-dimensional water exchanges in the shelf circulation system of the Northern South China Sea under climatic modulation from ENSO
<p>Three-dimensional water exchanges in the shelf circulation system of the Northern South China Sea under climatic modulation from ENSO</p>
Fig. 1 in Distributional Range Extension of Xeniamia atrithorax (Perciformes: Apogonidae) in the northern South China Sea
Fig. 1. Fresh specimens of Xeniamia atrithorax, collected off Dong-gang, Pingtung, Taiwan. (A, B) KAUM–I. 109976, 29.9 mm SL; (C, D) KAUM–I. 110317, 28.1 mm SL.
A dataset of archaeobotanical macroremains (staple crops) during the Neolithic and Bronze Ages in northern China
<p>Dataset of archaeobotanical macroremains includes a total of 538 flotation results from 381 sites with millets excavated during the Neolithic and Bronze Ages in northern China. Two steps of screening have been applied to eliminate inapplicable sites. The dataset only consisted of staple crops according to traditional Chinese agriculture: foxtail millet (Setaria italica), broomcorn millet (<em>Panicum miliaceum</em>), rice (<em>Oryza sativa</em>), wheat and barley (<em>Triticum aestivum</em> and <em>Hordeum vulgare</em>), and soybean (<em>Glycine max</em>). Informations of absolute counts and weights of staple crops, percentage of counts and weights for each site together with their locations and ages were assembled.</p>
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.