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309 results for “Yellow Sea”
Yellow-Bellied Sea Snake (Hydrophis platurus) brain illustration
<p>3D model of the Yellow-Bellied Sea Snake brain highlighting the anatomy and the spatial arrangement of its major subdivisions.</p> <p>The brain reconstruction was obtained from a microCT scan of a iodine-stained specimen through manual segmentation using the software Amira 5.5.0.</p> <p>Other illustrations can be found <strong><a href="https://zenodo.org/search?page=1&size=20&q=keywords:%22squamate%20brain%22">here</a></strong>.</p> <p><em>If you are interested in reptile brain evolution and behavior, please, have a look to our recent publication:</em></p> <p><a href="https://www.nature.com/articles/s41467-019-13405-w"><em><strong>"Comparative analysis of squamate brains unveils multi-level variation in cerebellar architecture associated with locomotor specialization"</strong></em></a></p> <p><strong>Simone Macrì, Yoland Savriama, Imran Khan & Nicolas Di-Poï</strong></p> <p><em>Nature Communications</em> <strong>10, </strong>5560 (2019)</p> <p> </p> <p><em>Check out also our *4K* video collection of various snake and lizard 3D brains:</em></p> <p><strong><a href="https://www.youtube.com/playlist?list=PLgx4vtT32C8hqxG_icKiuXGtZVLVX-oG1">Snake and Lizard brain reconstructions video collection</a></strong></p> <p> </p> <p>For any inquiries or additional information, please, refer to the contacts provided in the <strong><a href="https://www.nature.com/articles/s41467-019-13405-w">article</a></strong>.</p>
Water Body Checklists 2019: Yellow Sea Species List
Species checklists created using effechecka and modified polygons from IHO. The polygons were reduced in resolution.<p></p>List of species collected from the Yellow Sea using effechecka and a modified polygon from the International Hydrographic Association. A filter was applied (based on data from WoRMS) to remove all non-marine taxa.
Water Body Checklists: Yellow Sea Species List
Species checklists created using effechecka and modified polygons from IHO. The polygons were reduced in resolution.<p></p>List of species collected from the Yellow Sea using effechecka and a modified polygon from the International Hydrographic Association. A filter was applied (based on data from WoRMS) to remove all non-marine taxa.
Influences of the 1855 AD Huanghe (Yellow River) Relocation on Sedimentary Organic Carbon Burial in the Southern Yellow Sea
<p>This is the original data used in the manuscript titled "Influences of the 1855 AD Huanghe (Yellow River) Relocation on Sedimentary Organic Carbon Burial in the Southern Yellow Sea" which has been accepted by Frontiers in Marine Science. The data is from a box-core HH12 recovered from the southern Yellow Sea (123.50°E, 35.00°N; core length: 48 cm; water depth: 77 m; time span: ~300 yr). This excel includes depth, year, TOC, TN, biomarkers and other proxy record.</p> <p>Full Article at: <a href="https://www.frontiersin.org/articles/10.3389/fmars.2022.824617/full">https://www.frontiersin.org/articles/10.3389/fmars.2022.824617/full</a></p>
Fig. 4 in Distribution Of Sibling Species Yellow-Legged Gull, Larus Michahellis And Caspian Gull, Larus Cachinnans (Charadriiformes, Laridae), On The Black Sea Coast
Fig. 4. Settlements of Larus cachinnans (circles) and Larus michahellis (triangles) in the northern part of the Black Sea. Yellow figures — the species was determined by means of the analysis of mitochondrial DNA, red ones — by means of the analysis of museum specimens or photos of alive birds. According to Belik, 2018; Klein, Buchheim, 1997; Kuzikov, 2021; Liebers et al., 2004; Mnatsekanov et al., 1992; Sikorsky, 2016; Siokhin et al., 2000; Til'ba, Filipov, 2016; Tsvelykh, 2016, 2018 and data from this study.
Fig. 5 in Distribution Of Sibling Species Yellow-Legged Gull, Larus Michahellis And Caspian Gull, Larus Cachinnans (Charadriiformes, Laridae), On The Black Sea Coast
Fig. 5. Breeding ranges of Larus michahellis (orange) and Larus cachinnans (red) on the Black sea and Sea of Azov coasts.
Fig. 1 in Distribution Of Sibling Species Yellow-Legged Gull, Larus Michahellis And Caspian Gull, Larus Cachinnans (Charadriiformes, Laridae), On The Black Sea Coast
Fig. 1. Differences in coloration of the outer primaries of Larus michahellis (left column) and Larus cachinnans (right column) from the Black Sea coast. A — Kobuleti, Georgia. August 20, 1910 (collection of the National Museum of Natural History, the National Academy of Sciences of Ukraine), B — Karadag, Crimean Peninsula, Ukraine, July 2, 1946; (collection of the Zoological Museum of Kyiv National University), C — Vilkovo, Danube Delta, Ukraine, April 26, 1948 (collection of the Zoological Museum of Kyiv National University), D — Swan Islands, Karkinitian Bay, Ukraine, February 22, 1972 (collection of the National Museum of Natural History of the National Academy of Sciences of Ukraine).
Figure 1 in A new species of the genus Ethmolaimus de Man, 1880 (Nematoda, Ethmolaimidae) from intertidal zone of the Yellow Sea, China
Figure 1. Ethmolaimus multispiralis sp. nov. A. Anterior end of holotype, showing buccal cavity, teeth, cephalic setae, amphidial fovea and cuticle dots; B. Pharyngeal region of female, showing papilliform anterior sensilla, amphid, pharyngeal bulb and excretory system; C. Entire body of holotype; D. Cloacal region of holotype, showing spicule, lateral piece, gubernaculum and precloacal supplement; E. Entire body of female. Scale bars: A, B, D = 20 µm. C, E = 50 µm.
Figure 2 in A new species of the genus Ethmolaimus de Man, 1880 (Nematoda, Ethmolaimidae) from intertidal zone of the Yellow Sea, China
Figure 2. Ethmolaimus multispiralis sp. nov. A. Anterior end of holotype, showing buccal cavity, teeth, outer labial and cephalic setae; B. Anterior end of male, showing amphidial fovea and cuticle dots; C. Amphidial fovea of male; D. Pharyngeal bulb; E. Posterior portion of holotype, showing spicule and precloacal supplement; F. Cloacal region of holotype, showing spicule, lateral piece, gubernaculum and precloacal supplement. Scale bars: A–C = 10 µm; D–F = 20 µm.
Figure 3 in A new species of the genus Ethmolaimus de Man, 1880 (Nematoda, Ethmolaimidae) from intertidal zone of the Yellow Sea, China
Figure 3. Ethmolaimus multispiralis sp. nov. A. Lateral view of entire female; B. Anterior end of female, showing amphidial fovea (arrow) and cuticle punctation; C. Pharyngeal region of female, showing buccal cavity, anterior and posterior pharyngeal bulbs, and excretory system (arrows). Scale bars: A = 50 µm; B = 10 µm; C = 20 µm.
Figs 1−13. Ancistrum haliotis n in Two New and Two Poorly Known Species of Ancistrum (Ciliophora, Scuticociliatia, Thigmotrichida) Parasitizing Marine Molluscs from Chinese Coastal Waters of the Yellow Sea
Figs 1−13. Ancistrum haliotis n. sp. from the abalone Haliotis discus hannai Ino (1–5), Ancistrum mytili (Quennerstedt, 1867) from the blue mussel Mytilus edulis (6, after Kidder 1933) and the horse mussel Modiolus modiolus (7, after Hatzidimitriou and Berger 1977) and Ancistrum crassum Fenchel, 1965 from the purple clam Saxidomus purpuratus (Sowerby) (8–11) and from the short-necked clam Ruditapes philippinarum (12, 13, after Xu et al. 1997), from life (1, 2, 6, 8) and after protargol (3–5, 9, 10, 12, 13) and silver nitrate impregnation (7, 11). 1 – left lateral view of a representative specimen; 2, 3 – ventral view to show the oral structure; 4, 5 – left and right lateral view of the holotype specimen; 6, 7 – lateral and ventral view of A. mytili, which possesses a characteristic reniform macronucleus and a broad buccal field; 8 – left lateral view of body variants; 9–13 – lateral and ventral view of three specimens to show the ciliary pattern. CCo – caudal complex; CyP – cytoproct; M1–3 – membranelles 1–3; MA – macronucleus; MI – micronucleus; PM – paroral membrane; Sc – scutica; SK1, n – somatic kineties 1, n. Scale bars: 30 µm (4, 5 and 7, 9–13 drawn to scale).
Figs 14–25. Ancistrum acutum n in Two New and Two Poorly Known Species of Ancistrum (Ciliophora, Scuticociliatia, Thigmotrichida) Parasitizing Marine Molluscs from Chinese Coastal Waters of the Yellow Sea
Figs 14–25. Ancistrum acutum n. sp. from the surf clam Mactra veneriformis (14–17) and Ancistrum japonicum Uyemura, 1937 from the Japanese dosinia Dosinia japonica (18, 19, 21, 22) and the clam Cyclina sinensis (20, 23–25), from life (14, 15, 18–20) and after protargol (23–25) and silver nitrate impregnation (16, 17, 21, 22). 14 – left lateral view of a representative specimen; 15 – body variant and cortical granules; 16, 17 – ventral and dorsal view of the holotype specimen; 18, 19 – lateral view of living cells; 20 – lateral view of a representative specimen; 21, 22 – lateral view of same specimen; 23 – ventral ciliature; 24, 25 – lateral view of the neotype specimen. CCo – caudal complex; Cs – cytostome; CVP – contractile vacuole pore; M1–3 – membranelles 1–3; MA – macronucleus; MI – micronucleus; PM – paroral membrane; Sc – scutica; SK1, n – somatic kineties 1, n. Scale bars: 30 µm.
Fig. 2 in Data on Ten New Myxosporean Parasites (Myxozoa, Myxosporea, Bivalvulida) from the Yellow Sea, China
Fig. 2. Schematic illustrations of Ceratomyxa kareus sp. n. A–L – from Kareius bicoloratus; M–N – from Zebrias zebra; A–D – lateral view of mature spore; E–F, N – plasmodia with two spores; G–J – earlier stage plasmodia; K – plasmodium with one spore; L–M – plasmodia with mature spores. Scale bars: 10 µm.
Fig. 3 in Data on Ten New Myxosporean Parasites (Myxozoa, Myxosporea, Bivalvulida) from the Yellow Sea, China
Fig. 3. Schematic illustrations of Ceratomyxa spp. A–E – Ceratomyxa lomi sp. n.; A – mature spore viewed from the perspective of the capsule; B–D – lateral view of mature spore; E – plasmodium with two mature spores; F–J – Ceratomyxa lateolabrax sp. n.; F – plasmodium with two spores; G–J – lateral view of mature spore; K–N – Ceratomyxa qingdaoensis sp. n.; K–L, N – showing a lateral view of a mature spore; M – lateral view of an immature spore. Scale bars: 10 µm.
Fig. 1 in Data on Ten New Myxosporean Parasites (Myxozoa, Myxosporea, Bivalvulida) from the Yellow Sea, China
Fig. 1. Schematic illustrations of three myxosporean species. A–E – Sphaerospora sebasta sp. n.; A – mature spore from a frontal view; B–C – spore viewed from the perspective of the capsule; D – spore from a sutural view; E – spore from an oblique sutural view; F–H – Ceratomyxa sebastisca sp. n., showing mature spores with coarse sporoplasm; I–O – Ceratomyxa hemitriptera sp. n.; I–J – mature spore from a lateral view; K–L – plasmodium with one mature spore; M–N – early stage plasmodium with one developing spore; O – plasmodium with one developing spore from a capsule view. Scale bars: 10 µm.
Fig. 5 in Data on Ten New Myxosporean Parasites (Myxozoa, Myxosporea, Bivalvulida) from the Yellow Sea, China
Fig. 5. Microphotographs of myxosporean species. A–B – Sphaerospora sebasta sp. n.; C – Ceratomyxa sebastisca sp. n.; D–E – Ceratomyxa hemitriptera sp. n.; F–H – Ceratomyxa kareus sp. n.; I–J – Ceratomyxa lomi sp. n. Scale bars: 10 µm.
Fig. 4 in Data on Ten New Myxosporean Parasites (Myxozoa, Myxosporea, Bivalvulida) from the Yellow Sea, China
Fig. 4. Schematic illustrations of Ceratomyxa spp. A–G – Ceratomyxa saurida sp. n.; A–D, G – lateral view of mature spore; E – lateral view of abnormal spore; F – lateral view of immature spore; H–L – Ceratomyxa simplex sp. n.; H, J – lateral view of mature spore; I – immature spore viewed from the perspective of the capsule; K–L – plasmodia with one spore; M–T – Ceratomyxa triacantha sp. n.; M–N, P – plasmodia with two spores; O, Q – early stage plasmodia with many nuclei; R–T – sutural view of mature spores. Scale bars: 10 µm.
Fig. 1 in Biodiversity variability of macrobenthic in the Yellow Sea and East China Sea between 2001 and 2011
Fig. 1. Sampling stations in the Yellow Sea and East China Sea in March 2001, copied from the "Field work plan notice of 2001 spring cruise of the National Basic Research Program of China (19990437). YS, the subarea Yellow Sea. ECS, the subarea East China Sea. CJE, the subarea Changjiang River Estuary. Stations marked with red colour, the matching stations.
Figs 6–7 in Biodiversity variability of macrobenthic in the Yellow Sea and East China Sea between 2001 and 2011
Figs 6–7. Distribution of secondary productivity of macrobenthos. 6. In April 2011. 7. In August 2011.
Figs 3–4 in Biodiversity variability of macrobenthic in the Yellow Sea and East China Sea between 2001 and 2011
Figs 3–4. Horizontal distributions of macrobenthic abundance (ind/m2). 3. In March 2001. 4. In April 2011.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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