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1,109 results for “South China Sea”
Fig. 10. A–C in Deep-sea spider crabs of the families Epialtidae MacLeay, 1838 and Inachidae MacLeay, 1838, from the South China Sea, with descriptions of two new species (Decapoda, Brachyura, Majoidea)
Fig. 10. A–C. Rochinia kagoshimensis (Rathbun, 1932), holotype, ♂ (11.2 × 6.8 mm) (USNM 48253), off Kagoshima gulf. A. Overall dorsal view. B. Overall ventral view. C. Lateral view of carapace. D–F. Rochinia kagoshimensis (Rathbun 1932) comb. nov., ♂ (10.7 × 6.9 mm) (ZRC 2016.0549), South China Sea. D. Overall dorsal view. E. Overall ventral view. F. Lateral view of carapace. Scale bars = 5 mm.
Fig. 1 in Deep-sea spider crabs of the families Epialtidae MacLeay, 1838 and Inachidae MacLeay, 1838, from the South China Sea, with descriptions of two new species (Decapoda, Brachyura, Majoidea)
Fig. 1. Goniopugettia sagamiensis (Gordon, 1930), ♀ (41.8 × 30.1 mm) (ZRC 2016.0064), South China Sea with carapace half cleaned, left side of carapace with zootharian attached. A. Overall dorsal view. B. Lateral view of carapace. Scale bars = 10 mm.
Net community production, nutrients, and hydrographic parameters in the South China Sea in October 2014 and June 2015
<p>Net community production (NCP) corresponds to the difference between photosynthesis and respiration and can be estimated based on the dissolved oxygen to argon ratio (O<sub>2</sub>/Ar) in the mixed layer. NCP is also an important proxy for the biological pump in the ocean. In order to figure out the influencing factors on NCP in the northern slope region of the South China Sea (SCS), we conducted high-resolution underway measurements of O<sub>2</sub>/Ar and hydrographic parameters using membrane inlet mass spectrometry (MIMS) and multi-parameter water quality logger (RBR Maestro) in the northern slope region of the SCS in October 2014 and June 2015, assisted by nutrients measurements. NCP in the mixed layer was estimated using the biological supersaturation of O<sub>2</sub>/Ar, Δ (O<sub>2</sub>/Ar), and gas transfer velocity (k). All the underway data were compiled into the 5-min interval. Surface water samples for the nutrients analysis were collected from Niskin bottles mounted on the conductivity–temperature–depth (CTD) rosette at sampling stations, the nutrients were then photometrically determined by an auto-analyzer. The mixed layer depth (MLD) and the euphotic depth (Z<sub>eu</sub>) were calculated at stations where CTD casts were made based on potential density and chlorophyll fluorescence profile, respectively.</p>
Fig. 7 in Species Composition And Distribution Of The Dominant Flyingfishes (Exocoetidae) Associated With The Kuroshio Current, South China Sea
Fig. 7. Monthly median (square dot) with 25 th and 75th quartiles (vertical line) for (a) flyingfishes catch proportion (proportion of catch, adjusted by number of trips in the month, to the overall catches of the sampling year), (b) SST (°C), (c) tide level (cm), and (d) tidal range (cm). Tidal range in the plot is the difference of tide level within one hour. Dashed lines indicate roughly the area with high catch
Fig. 5 in Species Composition And Distribution Of The Dominant Flyingfishes (Exocoetidae) Associated With The Kuroshio Current, South China Sea
Fig. 5. Monthly flyingfish densities by (a) vertical catch layer (upper: Fig. 4. Flyingfish compositions of the six dominant species by 0–1.2 m, middle: 1.2–2.4 m, and bottom: 2.4–3.6 m), and (b) mesh sampling area, collected by in-port sampling and at-sea survey size of net (5.6 cm, 4 cm, and 2.8 cm for large, medium, and small
Fig. 3 in Anthomastus nanhaiensis, new species, and Bathyalcyon robustum Versluys, 1906, two mushroom soft corals (Octocorallia: Coralliidae) from Zhenbei Seamount in the South China Sea
Fig. 3. Sclerites of Anthomastus nanhaiensis, new species. A, sclerites from autozooid tentacle tip; B, sclerites from tentacle base; C, sclerites from pharynx. Scale bars = 0.10 mm (A, B), and 0.05 mm (C).
Fig. 2 in Anthomastus nanhaiensis, new species, and Bathyalcyon robustum Versluys, 1906, two mushroom soft corals (Octocorallia: Coralliidae) from Zhenbei Seamount in the South China Sea
Fig. 2. Morphology of the holotype of Anthomastus nanhaiensis, new species. A, the animal in situ; B, an autozooid; C, the colony in top view; D, the colony in lateral view; E, the longitudinal section of the colony, showing large cavities of autozooids (au) and small cavities of siphonozooids (arrows). Scale bars = 1 mm (B), 10 mm (C‒E).
Fig. 7 in Anthomastus nanhaiensis, new species, and Bathyalcyon robustum Versluys, 1906, two mushroom soft corals (Octocorallia: Coralliidae) from Zhenbei Seamount in the South China Sea
Fig. 7. Sclerites of Bathyalcyon robustum Versluys, 1906. A, sclerites from tentacle pinnules of autozooids; B, sclerites from tentacle rachis of autozooids; C, sclerites from anthocodial wall. Scale bars = 0.10 mm.
Fig. 8 in Anthomastus nanhaiensis, new species, and Bathyalcyon robustum Versluys, 1906, two mushroom soft corals (Octocorallia: Coralliidae) from Zhenbei Seamount in the South China Sea
Fig. 8. Sclerites of Bathyalcyon robustum Versluys, 1906. A, sclerites from pharynx; B, sclerites from outermost anthostelar coenenchyme; C, sclerites from deeper layer of coenenchyme; D, sclerites from holdfast. Scale bars = 0.10 mm.
Fig. 5 in Anthomastus nanhaiensis, new species, and Bathyalcyon robustum Versluys, 1906, two mushroom soft corals (Octocorallia: Coralliidae) from Zhenbei Seamount in the South China Sea
Fig. 5. Sclerites of Anthomastus nanhaiensis, new species. A, sclerites from surface of stalk; B, sclerites from interior of stalk. Scale bars = 0.10 mm.
Fig. 4 in Anthomastus nanhaiensis, new species, and Bathyalcyon robustum Versluys, 1906, two mushroom soft corals (Octocorallia: Coralliidae) from Zhenbei Seamount in the South China Sea
Fig. 4. Sclerites of Anthomastus nanhaiensis, new species. A, sclerites from surface of capitulum; B, sclerites from interior of capitulum. Scale bars = 0.10 mm.
Fig. 6 in Anthomastus nanhaiensis, new species, and Bathyalcyon robustum Versluys, 1906, two mushroom soft corals (Octocorallia: Coralliidae) from Zhenbei Seamount in the South China Sea
Fig. 6. Morphology of Bathyalcyon robustum Versluys, 1906. A, MBM286427 in situ; B, clonies in aggregation with MBM286428 in the most right; C, MBM286427 in preservation; D, MBM286428 in preservation; E, siphonozooids; F, transverse section through middle anthostele of MBM286427, showing pharynx and mesenteries. Scale bars = 10 mm (C, D), 0.5 mm (E), and 5 mm (F).
FIGURE 3 Holotype NMNS-8130-001 in Phylogeny of two new pheronematid sponges from the Caroline Seamount and South China Sea
FIGURE 3 Holotype NMNS-8130-001 of Pheronemoides curvipentactin sp. nov. A, the external morphology of dermal areas (scale bar = 5 cm); B, the external morphology of atrial areas.
FIGURE 4 in Phylogeny of two new pheronematid sponges from the Caroline Seamount and South China Sea
FIGURE 4 Spicules of holotype NMNS-8130-001 of Pheronemoides curvipentactin sp. nov. A, choanosomal pentactin; B–C, dermal pinular pentactins; D–H, atrialia: D–E, pinular pentactins; F, crooked pentactin; G–H, special pentactins; I, shaft of macrouncinate; J, microuncinate; K, shaft of microuncinate; L, terminal of microuncinate; M, micramphidisc; N, microdiactin; O–Q, the anchor of basalia; R–S; marginalia.
FIGURE 5 in Phylogeny of two new pheronematid sponges from the Caroline Seamount and South China Sea
FIGURE 5 Bayesian inference trees of pheronematid species based on the 16S rDNA and 28S rDNA sequence data. Numbers at each node are Bayesian posterior probabilities (left) and ML analysis bootstrap values (right).
FIGURE 1 Holotype MBM286618 in Phylogeny of two new pheronematid sponges from the Caroline Seamount and South China Sea
FIGURE 1 Holotype MBM286618 of Pheronemoides crustiformis sp. nov. A, photograph showing the specimen in its natural habitat; B, the external morphology of atrial areas; C, the external morphology of dermal areas and basalia; D, mesh structure of dermal areas; E, mesh structure of atrial areas.
FIGURE 2 in Phylogeny of two new pheronematid sponges from the Caroline Seamount and South China Sea
FIGURE 2 Spicules of holotype MBM286618 of Pheronemoides crustiformis sp. nov. A, choanosomal pentactin; B, the anchor of basalia; C, atrial pinular pentactin; D, dermal pinular pentactin; E–G, micramphidiscs; H, microdiactin I; I, microdiactin II; J, shaft of macrouncinate; K, shaft of mesouncinate; L–N, Sceptre; O–P, the anchor of basalia.
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>
Figure 6. Vellumnus tki n in Redescription of Vellumnus penicillatus (Gordon, 1930) from Hong Kong and description of a new species from Macclesfield Bank, South China Sea (Crustacea: Brachyura: Pilumnidae)
Figure 6. Vellumnus tki n. sp., holotype male (7.8 × 6.0 mm) (NHM 1932.7.7.22), Macclesfield Bank. A, Right side of denuded carapace; B, front, epistome, antennule, antenna and orbit; C, left third maxilliped (denuded); D, left fourth ambulatory leg (denuded); E, anterior thoracic sternum; F, pleon; G, left G1 (ventral view); H, distal part of left G1 (ventral view); I, tip of left G1 (ventral view); J, distal part of left G1 (dorsal view); K, left G2. Scales: A–F= 1.0 mm; G, J = 0.5 mm; H, I = 0.2 mm.
Figure 1 in Redescription of Vellumnus penicillatus (Gordon, 1930) from Hong Kong and description of a new species from Macclesfield Bank, South China Sea (Crustacea: Brachyura: Pilumnidae)
Figure 1. Vellumnus penicillatus (Gordon, 1930). A, Holotype female (4.2 × 2.9 mm) (NHM 1930.12.2.123), Hong Kong; B, C, paratype male (3.6 × 2.9 mm) (NHM 1930.12.2.124), Hong Kong. A, B, overall dorsal view; C, ventral view of cephalothorax.
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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.