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FIGURE 5 in Weltneria acanthostoma sp. nov., a burrowing barnacle (Cirripedia: Acrothoracica) from the deep-waters of the South China Sea
FIGURE 5. Map of distribution of species of Weltneria (modified after Kolbasov 2009): 1—W. aapta, 2—W. acanthostoma, 3—W. bekae, 4—W. exargilla, 5—W. griggi, 6—W. hessleri, 7—W. hirsuta, 8—W. ligamenta, 9—W. reticulata, 10—W. spinosa, 11—W. tomlinsoni, 12—W. zibrowii.
FIGURE 1 in Weltneria acanthostoma sp. nov., a burrowing barnacle (Cirripedia: Acrothoracica) from the deep-waters of the South China Sea
FIGURE 1. Weltneria acanthostoma sp. nov., general appearance (light microscopy). (A) General view, lateral side, part of mantle from rear side enlarged in rectangular area. (B) Opercular area, lateral view, parts of opercular bar with tiny bifid teeth and posterior margin of aperture with simple mantle teeth enlarged in rectangular areas. (C) Attachment disk separated from mantle sac, frontal view. (D) Posterior part of thorax with bases of terminal cirri and caudal appendages. Abbreviations: ad— attachment disk, ca—caudal appendages, ob—opercular bars, oc—oral/mouth cone, tc—terminal cirri. Scale bars in µm.
FIGURE 1. A–B in Recent brachiopods from the South China Sea, NW Pacific
FIGURE 1. A–B. Terebratulina japonica (Sowerby, 1846), dorsal views of complete specimens, stn DW 4125, 305–306 m, SEM, MNHN IB-2013-640. C–G. Macandrevia sp., one complete specimen, stn CP 4123, 1612–1665 m, MNHN IB-2013-641. C–D. Dorsal and lateral views of complete specimen. E–F. Ventral valve of the same specimen, posterior part of interior and tilted view to show strong dental plates, SEM. G. Interior view of dorsal valve to show cardinalia, SEM. H–R. Nipponithyris afra Cooper, 1973, stn CP 4130, 795–822 m. H–M. Dorsal, lateral and anterior views of two complete specimens, MNHN BI-2013-642. N–O. Posterior part of ventral valve interior and tilted view to show swollen bases and grooves to accommodate inner socket ridges, SEM, MNHN BI-2013- 643. P. Interior of dorsal valve, partly broken loop visible, SEM, MNHN BI-2013-644. Q–R. Posterior part of dorsal valve interior and enlargement to show details of strongly thickened cardinalia, SEM MNHN BI-2013-645.
FIGURE 4 in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea
FIGURE 4. Unmatched sites from SSrRNA gene sequences alignment. Numbers represent the positions of the nucleotides. Missing sites are compensated by gaps (-). Matched sites are marked with dots (.).
FIGURE 3 in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea
FIGURE 3. Comparison of Apokeronopsis species. A. crassa (A, B, from Song et al. 2004), A. wrighti (C, D, from Long et al. 2008), A. antarctica (E, F, from Petz 1995), A. ovalis (G, H, from Shao et al. 2009), A. bergeri (I, J, from Li et al. 2008), and A. sinica (K, L, original), to show the morphology of live cells (A, C, E, G, I, K), infraciliature (B, D, F, H, J, L). Scale bars in (A, B, I, J) =100 µm, in (C–H, K, L) = 60 µm.
FIGURE 2 in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea
FIGURE 2. Photomicrographs of Apokeronopsis sinica n. sp. from live cells (A–E, I, J) and after protargol impregnation (K–O), and ventral views of live cells of A. crassa (F), A. bergeri (G) and A. wrighti (H). (A) Ventral view of the typical specimen. (B) Ventral view, showing the contractile vacuole (arrow). (C) Lateral view. (D) Ventral view of the anterior portion, arrows indicate the cilia of adoral zone of membranelles, arrowheads mark the paroral membranes and double-arrowheads depict the buccal cirri. (E) Lateral view to show the large cortical granules distributed on dorsal side. (I) Ventral view, to show the cortical granules: vermeil large (arrows), colorless large (arrowheads) and colorless small ones (double-arrowheads). (J) Ventral view, showing the cortical granules between the cirri rows. (K) infraciliature of the ventral side of a typical specimen. (L) Ventral view of the anterior portion, arrow indicates the paroral membrane and arrowhead marks the endoral membrane. (M) Ventral view of the anterior-right portion, arrowheads refer to frontoterminal cirri, and arrows show the buccal cirri. (N) Macronuclear nodules. (O) Ventral view of the posterior portion, note the transverse cirri (arrows). Scale bars in (A, B, C, F, G, H) = 100 µm, in (K) = 80 µm.
FIGURE 1. Apokeronopsis sinica n in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea
FIGURE 1. Apokeronopsis sinica n. sp. from live cells (A–D) and after protargol impregnation (E–F). (A, B) Ventral views of two typical specimens. (C) Dorsal view; to show the sparsely distributed large granules. (D) Details of the cortex, double-arrowheads indicate the smaller cortical granules, arrows mark the vermeil larger ones and arrowheads mark the colorless larger ones. (E, F) Ventral and dorsal views of the infraciliature and nuclear apparatus. AZM = adoral zone of membranelles; BC = buccal cirri; BiC = bicoronal cirri; DK = dorsal kineties; EM = endoral membrane; FTC = frontoterminal cirri; LMR = left marginal row; Ma = macronuclei; MC = midventral complex; PM = paroral membrane; RMR = right marginal row; TC = transverse cirri. Scale bars = 80 µm.
FIGURE 6. A in A new barbeled goby from south China (Teleostei: Gobiidae)
FIGURE 6. A phylogenetic tree based on an alignment of 887bp 12s rDNA containing 12.92% missing data of 8 Tridentiger species, topology and branch lengths obtained by MrBayes is shown. Nodal support values are given in the following order: Posterior probability of BS tree, 1000 bootstrap of RAxML tree. Poorly supported nodes (PP <70%) are marked with a "*".
FIGURE 5 in A new barbeled goby from south China (Teleostei: Gobiidae)
FIGURE 5. Linear regressions of standard length and natural log-transformed wet body weight for T. radiatus (n=191), T. bifasciatus (n=137) and T. barbatus (n=511). Grey regions depict 95% CI of the least-square regression line. See Table 3 for parameter estimates.
FIGURE 4 in A new barbeled goby from south China (Teleostei: Gobiidae)
FIGURE 4. Lateral view of T. radiatus displaying facial barbel and papilla pattern. Nomenclature of sensory canal pores same as Figure 2. Sanzo, 1911 is adopted for the nomenclature of papillae and barbels rows. Pore A' blocked by anterior nasal tubule from this angle, not shown.
FIGURE 1 in A new barbeled goby from south China (Teleostei: Gobiidae)
FIGURE 1. Photographs of fresh Tridentiger radiatus sp. nov. and T. barbatus specimens. A. Lateral view of T. radiatus (Holotype, SYSZ0030838, Male, SL=64.2 mm); B. Lateral view of T. barbatus (SYSZ0030812 Male, SL=73.7 mm); C. Ventral view of the same specimen of T. radiatus, arrow showing less developed chin barbels; D. Ventral view of the same specimen of T. barbatus, arrow referring to the highly developed chin barbels; E. Dorsal view of T. radiatus (Paratype, SYSZ0030836, Male, SL=77.8 mm) showing a banded colouration.
FIGURE 3 in A new barbeled goby from south China (Teleostei: Gobiidae)
FIGURE 3. Ventral view of T. radiatus displaying ventral barbel lines. Nomenclature adopted from homologous papillae lines in Sanzo, 1911, e: linea exteriore, i: linea interiore. CM: Centre-most chin barbel.
FIGURE 2 in A new barbeled goby from south China (Teleostei: Gobiidae)
FIGURE 2. Cephalic canal system and sensory pores of Tridentiger radiatus. AN: Anterior nasal pore, PN: Posterior nasal pore, AOC: Anterior oculoscapular canal, POC: Posterior oculoscapular canal, PC: Preopercular canal. Nomenclature of sensory pores follows (Akihito et al. 1988), canals are marked by dotted lines.
Figure 2 in Morphology and molecular phylogeny of three new oligotrich ciliates (Protozoa, Ciliophora) from the South China Sea
Figure 2. Parallelostrombidium ellipticum sp. nov. from life (A–F, J–R) and after protargol impregnation (G–I, S–Y). A, J, ventral views of typical specimen. B, L, dorsal views, arrowhead marks the extrosomes. C, P, detail views of the polygonal platelets. D, resting extrusomes. E, swimming trace. F, K, fat individual. G, pattern of somatic ciliature. H, I, ventral (H) and dorsal (I) views showing the ciliary pattern and the macronucleus. M, Q, apical views, arrows mark the thigmotactic membranelles. N, ventral view of anterior portion of cell, arrow marks the apical protrusion. O, detail of extrusomes attached above the girdle kinety, arrowheads mark the cilia of girdle kinety. R, S, posterior portion of cell, showing the distribution of extrusomes (arrowheads). T, detail view of the dikinetids in girdle kinety. U, Y, right lateral views to show the posterior portion of ventral and girdle kineties. V, ventral view showing the somatic kineties and the macronucleus. W, ventral views of anterior cell portion, to show the adoral zone of membranelles. X, detail of the oral primordium (arrow) in the early stage dividers. AM, anterior membranelles; E, extrusomes; EM, endoral membrane; GK, girdle kinety; Ma, macronucleus; TM, thigmotactic membranelles; VK, ventral kinety; VM, ventral membranelles. Scale bars: 100 μm (E); 30 μm (A, B, F–M, Q); 20 μm (N, R, S, U–W); 5 μm (C, D, O, P, T, X, Y).
Figure 4 in Morphology and molecular phylogeny of three new oligotrich ciliates (Protozoa, Ciliophora) from the South China Sea
Figure 4. Maximum likelihood (ML) tree inferred from small subunit (SSU) rRNA gene sequences indicating the phylogenetic positions of Parallelostrombidium obesum, Parallelostrombidium ellipticum, and Strombidium tropicum (orange dots). Numbers at the nodes represent support values in the following order: ML bootstrap values and Bayesian inference (BI) posterior probabilities. Nodes absent from one of the two phylogenies are indicated by a hyphen. The scale bar indicates the number of substitutions per ten nucleotides.
Figure 1 in Morphology and molecular phylogeny of three new oligotrich ciliates (Protozoa, Ciliophora) from the South China Sea
Figure 1. Parallelostrombidium obesum sp. nov. from life (A–E, I–R) and after protargol impregnation (F–H, S–V). A, ventral view of typical specimen. B, I, J, different body shapes, arrow marks the apical protrusion. C, swimming trace. D, P, pattern of cortical platelets. E, O, Q, detail of extrusomes attached above the girdle kinety. F, pattern of somatic ciliature. G, H, ventral (G) and dorsal (H) views of the same specimens showing the ciliary pattern and the macronucleus. K, lateral view. L, N, ventral (L) and dorsal (N) views showing the distribution of extrusomes (arrowheads). M, two thigmotactic membranelles. R, detail of bases of thigmotactic membranelles (arrows). S, V, ventral views of anterior portion of cell showing oral membranelles. T, U, dorsal (T) and ventral (U) views showing the girdle and ventral kineties. AM, anterior membranelles; E, extrusomes; EM, endoral membrane; GK, girdle kinety; Ma, macronucleus; TM, thigmotactic membranelles; VK, ventral kinety; VM, ventral membranelles. Scale bars: 120 μm (C); 40 μm (A, B, F–K); 20 μm (L–N, S–V); 10 μm (D, E, O–R).
Figure 3 in Morphology and molecular phylogeny of three new oligotrich ciliates (Protozoa, Ciliophora) from the South China Sea
Figure 3. Strombidium tropicum sp. nov. from life (A–D, J–P) and after protargol impregnation (E–I, Q–V). A, ventral view of a representative specimen. B, J–L, different body shapes, arrow marks the apical protrusion. C, P, resting extrusomes. D, swimming trace. E, detail of dikinetids, arrow and arrowhead mark the argyrophilic fibres associated with dikinetids in girdle and ventral kineties, respectively. F, detail of ventral membranelles and argyrophilic fibres. G–I, ventral (G, H) and dorsal (I) views showing the ciliary pattern and the macronucleus, arrow marks the argyrophilic fibres associated with adoral membranellar zone and arrowhead notes the pharyngeal fibres. M, ventral view of a mid-divider, arrow shows the oral primordium. N, apical view showing the adoral zone of membranelles. O, dorsal view showing the distribution of extrusomes (arrow). Q, the macronucleus. R, U, ventral views of adoral zone of membranelles, arrow marks the argyrophilic fibres. S, V, ventral and dorsal views of posterior portion of cells to show the infraciliature, arrow marks the extrosomes and arrowhead notes the hemitheca. T, detail of girdle kinety, arrow shows the argyrophilic fibres and arrowhead marks the cilium. AM, anterior membranelles; E, extrusomes; EM, endoral membrane; GK, girdle kinety; Ma, macronucleus; VK, ventral kinety; VM, ventral membranelles. Scale bars: 50 μm (D); 10 μm (A, B, G–L, N, O, Q), 5 μm (C, F, M, P, R, S, U, V), 2 μm (E, T).
Annual-resolution Sr/Ca records of fossil Porites corals from the northern South China Sea
<p>This dataset reports thirteen annual-resolution Sr/Ca records and seven 10-yr resolution Sr/Ca records of a total of 20 fossil <i>Porites </i>corals collected from the northern South China Sea. The ages of the fossil corals were determined by U-Th geochemistry. The Sr/Ca measurements were carried out using an Inductively Coupled Plasma-optical emission spectroscopy (ICP-OES; Agilent 5110). The international coral standard JCp-1 was measured along with the samples, yielding an average value of 8.839 ± 0.017 mmol/mol (1 SD, n = 36).</p>
FIGURE 5 in A new species of the coral-symbiont crab genus Cymo de Haan, 1833 (Decapoda, Brachyura, Xanthidae) from Nansha Islands, the South China Sea
FIGURE 5. Diagnostic features of Cymo: A, F, K, P, C. mazu sp. nov.; B, G, L, Q, C. deplanatus; C, H, M, R, C. quadrilobatus; D, I, N, S, C. andreossyi; E, J, O, T, C. melanodactylus; A–E, overall morphology and live coloration; F–G, front; K–O, major cheliped; P–T, maxilliped 1. Scale bars: A, J, L, M = 2 mm; B–D, N, O = 5 mm; E = 10 mm; F, P = 0.5 mm; G–I, K, Q–T = 1 mm.
FIGURE 3 in A new species of the coral-symbiont crab genus Cymo de Haan, 1833 (Decapoda, Brachyura, Xanthidae) from Nansha Islands, the South China Sea
FIGURE 3. Cymo mazu sp. nov., holotype, male, CW 4.1 mm, CL 3.8 mm, MBM287035: A, carapace; B, front; C, maxilliped 1; D, maxilliped 3; E, pereopod 5; F, large cheliped; G, pleon; H, left G1, ventral view; I, left G1, distal part, ventral view; J, same, dorsal view; K, right G2, ventral view. Scale bar A, E, F = 1 mm, C, D, G = 0.5 mm, H = 0.2 mm, I–K = 0.1 mm.
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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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.