Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
2,510
datasets available to search
ShareScore release 0.9.0
Dataset results
2,510 results for “South China”
FIGURE 7 in Three new species of shell-boring Dipolydora (Annelida: Spionidae: Polydorini) from the South China Sea and the Gulf of Thailand, Vietnam, with comments on the modified spines in posterior notopodia and sperm morphology in polydorins
FIGURE 7. Morphology of Dipolydora spinosa sp. nov. A–D, anterior ends: A, left lateral view; B, D, ventral view; C, dorsal view. E–G, posterior ends: E, left lateral view; F, dorsal view; G, dorso-lateral view. H, notopodia of posterior chaetigers with capillary chaetae and awl-like spines. Abbreviation: an = occipital antenna, ch5 = chaetiger 5. Scale bars: A–D = 300 µm; E–G = 200 µm; H = 50 µm. A–F—holotype MIMB 42721, in life; G, H—paratype MIMB 42720, in life.
FIGURE 6 in Three new species of shell-boring Dipolydora (Annelida: Spionidae: Polydorini) from the South China Sea and the Gulf of Thailand, Vietnam, with comments on the modified spines in posterior notopodia and sperm morphology in polydorins
FIGURE 6. Dipolydora spinosa sp. nov. morphometric relationships. A, caruncle length and anterior position of gizzard-like structure versus total number of chaetigers. B, last branchiate chaetiger and anterior position of notopodial awl-like spines versus total number of chaetigers. Correlation coefficients (r) and their significance are reported in Table 1.
FIGURE 5 in Three new species of shell-boring Dipolydora (Annelida: Spionidae: Polydorini) from the South China Sea and the Gulf of Thailand, Vietnam, with comments on the modified spines in posterior notopodia and sperm morphology in polydorins
FIGURE 5. Morphology of Dipolydora spinosa sp. nov. (in life). A, B, anterior end, dorsal view. C, middle chaetigers, dorsal view, showing gizzard-like structure. D, gizzard-like structure, dorsal view, showing grain-like structures in the wall. Abbreviation: ch5 = chaetiger 5; gi = gizzard-lile structure. Scale bars: A–C = 200 µm; D = 50 µm. A, C, D—41-chaetiger individual; B—70-chaetiger individual. A–D—MIMB 42719.
FIGURE 3 in Three new species of shell-boring Dipolydora (Annelida: Spionidae: Polydorini) from the South China Sea and the Gulf of Thailand, Vietnam, with comments on the modified spines in posterior notopodia and sperm morphology in polydorins
FIGURE 3. Morphology of Dipolydora echinata sp. nov. (formalin-fixed holotype MIMB 42702 stained with methylene green). A, posterior end, dorsal view. B, notopodia of posterior chaetiger with thin protruding capillary chaetae and thick embedded awl-like spines. C, pygidium, dorsal view. Scale bars: A–C = 50 µm.
FIGURE 8 in Three new species of shell-boring Dipolydora (Annelida: Spionidae: Polydorini) from the South China Sea and the Gulf of Thailand, Vietnam, with comments on the modified spines in posterior notopodia and sperm morphology in polydorins
FIGURE 8. Morphology of Dipolydora spinosa sp. nov. A–F, chaetiger 5 chaetae: A, C, bilimbate companion chaetae; B, D, falcate spines in lateral view; E, ventral capillary chaeta; F, dorsal superior geniculate capillary chaeta. G, H, neurochaetae from chaetiger 7: G, inferior winged capillary chaeta; H, bidentate hooded hook. I, J, neurochaetae from a posterior most chaetiger: I, inferior hair-like capillary chaeta; J, bidentate hooded hook. K, L, notochaetae from a posterior most chaetiger: K, three awl-like spines with basal part blunt; L, capillary chaeta. M, octad of spermatids (one below is not visible). Scale bars: A–J, K, L = 20 µm; M = 5 µm. A–J—MIMB 42714; K–M—MIMB 42715.
FIGURE 2 in Three new species of shell-boring Dipolydora (Annelida: Spionidae: Polydorini) from the South China Sea and the Gulf of Thailand, Vietnam, with comments on the modified spines in posterior notopodia and sperm morphology in polydorins
FIGURE 2. Morphology of Dipolydora echinata sp. nov. A, anterior end, dorsal view. B–H, chaetiger 5 chaetae: B, D, bilimbate companion chaetae; C, E, F, falcate spines in lateral view (C, F) and in rear view (E); G, ventral capillary chaeta; H, dorsal superior geniculate capillary chaeta. I, J, neurochaetae from chaetiger 7: I, inferior winged capillary chaeta; J, bidentate hooded hook. K, L, neurochaetae from a posterior most chaetiger: K, inferior hair-like capillary chaeta; L, bidentate hooded hook. M–O, notochaetae from a posterior most chaetiger: M, partially developed awl-like spine with basal part blunt; N, fully developed awl-like spine with basal part pointed; O, capillary chaeta. P, tetrad of spermatids. Scale bars: A = 100 µm; B–O = 20 µm; P = 5 µm. A–P—MIMB 42701.
FIGURE 9 in Three new species of shell-boring Dipolydora (Annelida: Spionidae: Polydorini) from the South China Sea and the Gulf of Thailand, Vietnam, with comments on the modified spines in posterior notopodia and sperm morphology in polydorins
FIGURE 9. Morphology and reproduction of Dipolydora spinosa sp. nov. (in life). A, complete female, left lateral view, palps missing. B, anterior end, dorsal view, palps missing. C, a part of a brood laid by female inside its burrow in the shell, showing egg capsules joined in a string and containing trochophores. D, trochophores and abortive eggs from the capsules shown on C. Abbreviations: ab = abortive eggs; mo = mouth. Scale bars: A = 500 µm; B, C = 300 µm; D = 30 µm. A, B—paratype MIMB 42720; C, D—egg capsules deposited by holotype MIMB 42721.
FIGURE 1 in Three new species of shell-boring Dipolydora (Annelida: Spionidae: Polydorini) from the South China Sea and the Gulf of Thailand, Vietnam, with comments on the modified spines in posterior notopodia and sperm morphology in polydorins
FIGURE 1. Maps showing sampling locations in the Gulf of Thailand and South China Sea (A) and Nha Trang Bay (B).
FIGURE 4 in Three new species of shell-boring Dipolydora (Annelida: Spionidae: Polydorini) from the South China Sea and the Gulf of Thailand, Vietnam, with comments on the modified spines in posterior notopodia and sperm morphology in polydorins
FIGURE 4. Morphology of Dipolydora spinosa sp. nov. (formalin-fixed 41-chaetiger paratype MIMB 42719 stained with methylene green). A, anterior end, dorsal view. B, chaetigers 10–20, dorsal view, showing remains of larval pigmentation and pattern of MG staining. Abbreviations: ch10, ch20 = chaetigers 10 and 20; dl = dorso-lateral melanophores; do = dorsal paired melanophores; la = lateral melanophores; me = median vesiculate melanophores. Scale bars: A, B = 50 µm.
FIGURE 13 in Three new species of shell-boring Dipolydora (Annelida: Spionidae: Polydorini) from the South China Sea and the Gulf of Thailand, Vietnam, with comments on the modified spines in posterior notopodia and sperm morphology in polydorins
FIGURE 13. Morphology of Dipolydora vietnamita sp. nov. A–F, chaetiger 5 chaetae: A, C, bilimbate companion chaetae; B, D, falcate spines in lateral view; E, ventral capillary chaeta; F, dorsal superior geniculate capillary chaeta. G, H, neurochaetae from chaetiger 7: G, inferior winged capillary chaeta; H, bidentate hooded hook. I, J, neurochaetae from a posterior most chaetiger: I, inferior hair-like capillary chaeta; J, bidentate hooded hook. K, tetrad of spermatids. Scale bars: A–J = 20 µm; K = 5 µm. A–K—MIMB 42724.
Subspecies and Distribution. M. f. fascicularis Raffles, 1821 — S Laos, S Vietnam, Cambodia, E & S Thailand (and offshore Is), S to the Malay Peninsula, Borneo, Sumatra, Java, Bali, and most but not all offshore Is, also extending into the Sulu Archipelago and Zamboanga Peninsula of W Mindanao, in the Philippines; probably artificially introduced in the Nusa Penida-Timor Is chain. M. f. atriceps Kloss, 1919 — Ko Khram I (= Khram Yai), off SE coast of Thailand. M. f. aureus E. Geoffroy Saint-Hilaire, 1831 — SW Bangladesh (Teknaaf Peninsula), S Myanmar (including the Mergui Archipelago), WC Thailand (S to ¢.10° N), and Laos. M. f. condorensis Kloss, 1926 — SE Vietnam (Con Son and Hon Ba Is in the South China Sea). M. f. fuscus G. S. Miller, 1903 — Simeulue I, off NW Sumatra. M. f. karimondjawae Sody, 1949 — Karimunjawa I and presumably nearby Kemujan I, N ofJava. M. f. lasiae Lyon, 1916 — Lasia I, off NW Sumatra. M. f. philippinensis 1. Geoffroy Saint-Hilaire, 1843 — Philippine Archipelago N of ¢.10° N. M. f. tua Kellogg, 1944 — Maratua I, off E Borneo. M. f. umbrosus G. S. Miller, 1902 — Nicobar Is (Katchall, Little Nicobar, and Great Nicobar Is). in Cercopithecidae
Subspecies and Distribution. M. f. fascicularis Raffles, 1821 — S Laos, S Vietnam, Cambodia, E & S Thailand (and offshore Is), S to the Malay Peninsula, Borneo, Sumatra, Java, Bali, and most but not all offshore Is, also extending into the Sulu Archipelago and Zamboanga Peninsula of W Mindanao, in the Philippines; probably artificially introduced in the Nusa Penida-Timor Is chain. M. f. atriceps Kloss, 1919 — Ko Khram I (= Khram Yai), off SE coast of Thailand. M. f. aureus E. Geoffroy Saint-Hilaire, 1831 — SW Bangladesh (Teknaaf Peninsula), S Myanmar (including the Mergui Archipelago), WC Thailand (S to ¢.10° N), and Laos. M. f. condorensis Kloss, 1926 — SE Vietnam (Con Son and Hon Ba Is in the South China Sea). M. f. fuscus G. S. Miller, 1903 — Simeulue I, off NW Sumatra. M. f. karimondjawae Sody, 1949 — Karimunjawa I and presumably nearby Kemujan I, N ofJava. M. f. lasiae Lyon, 1916 — Lasia I, off NW Sumatra. M. f. philippinensis 1. Geoffroy Saint-Hilaire, 1843 — Philippine Archipelago N of ¢.10° N. M. f. tua Kellogg, 1944 — Maratua I, off E Borneo. M. f. umbrosus G. S. Miller, 1902 — Nicobar Is (Katchall, Little Nicobar, and Great Nicobar Is).
On following pages: 631. Ryukyu Islands Tree Rat (Diplothrix legata); 632. Lesser Bandicoot Rat (Bandicota bengalensis); 633. Greater Bandicoot Rat (Bandicota indica); 634. Savile's Bandicoot Rat (Bandicota savilei), 635. Mackenzie's White-toothed Rat (Berylmys mackenziel); 636. Manipur White-toothed Rat (Berylmys manipulus); 637. Bowers's White-toothed Rat (Berylmys bowersii); 638. Berdmore's White-toothed Rat (Bery/mys berdmorei); 639. Millard's Rat (Dacnomys millard)); 640. Brahman White-bellied Rat (Niviventer brahma); 641. Smoke-bellied White-bellied Rat (Niviventer eha); 642. Anderson's White-bellied Rat (Niviventer andersoni), 643. Sichuan White-bellied Rat (Niviventer excelsion); 644. South China White-bellied Rat (Niviventer huang); 645. Hainan White-bellied Rat (Niviventer lotipes); 646. Himalayan White-bellied Rat (Niviventer niviventen; 647. Spiny Taiwan White-bellied Rat (Niviventer coninga); 648. Soft-furred Taiwan White-bellied Rat (Niviventer culturatus), 649. Cameron Highlands White-bellied Rat (Niviventer cameron); 650. Indochinese White-bellied Rat (Niviventer fulvescens); 651. Bukit White-bellied Rat (Niviventer bukit); 652. Confucian White-bellied Rat (Niviventer confucianus); 653. Limestone White-bellied Rat (Niviventer hinpoon); 654. Indochinese Mountain White-bellied Rat (Niviventer tenaster); 655. Sundaic Arboreal White-bellied Rat (Niviventer cremoriventer); 656. Montane Sumatran White-bellied Rat (Niviventer fraternus);, 657. Montane Javan White-bellied Rat (Niviventer lepturus); 658. Montane Bornean White-bellied Rat (Niviventer rapit). in Muridae
On following pages: 631. Ryukyu Islands Tree Rat (Diplothrix legata); 632. Lesser Bandicoot Rat (Bandicota bengalensis); 633. Greater Bandicoot Rat (Bandicota indica); 634. Savile's Bandicoot Rat (Bandicota savilei), 635. Mackenzie's White-toothed Rat (Berylmys mackenziel); 636. Manipur White-toothed Rat (Berylmys manipulus); 637. Bowers's White-toothed Rat (Berylmys bowersii); 638. Berdmore's White-toothed Rat (Bery/mys berdmorei); 639. Millard's Rat (Dacnomys millard)); 640. Brahman White-bellied Rat (Niviventer brahma); 641. Smoke-bellied White-bellied Rat (Niviventer eha); 642. Anderson's White-bellied Rat (Niviventer andersoni), 643. Sichuan White-bellied Rat (Niviventer excelsion); 644. South China White-bellied Rat (Niviventer huang); 645. Hainan White-bellied Rat (Niviventer lotipes); 646. Himalayan White-bellied Rat (Niviventer niviventen; 647. Spiny Taiwan White-bellied Rat (Niviventer coninga); 648. Soft-furred Taiwan White-bellied Rat (Niviventer culturatus), 649. Cameron Highlands White-bellied Rat (Niviventer cameron); 650. Indochinese White-bellied Rat (Niviventer fulvescens); 651. Bukit White-bellied Rat (Niviventer bukit); 652. Confucian White-bellied Rat (Niviventer confucianus); 653. Limestone White-bellied Rat (Niviventer hinpoon); 654. Indochinese Mountain White-bellied Rat (Niviventer tenaster); 655. Sundaic Arboreal White-bellied Rat (Niviventer cremoriventer); 656. Montane Sumatran White-bellied Rat (Niviventer fraternus);, 657. Montane Javan White-bellied Rat (Niviventer lepturus); 658. Montane Bornean White-bellied Rat (Niviventer rapit).
On following pages: 507. Cansdale's Swamp Rat (Malacomys cansdalel); 508. Edwards's Swamp Rat (Malacomys edwards); 509. Alpine Field Mouse (Apodemus alpicola), 510. Long-tailed Field Mouse (Apodemus sylvaticus); 511. Striped Field Mouse (Apodemus agrarius); 512. Western Broad-toothed Field Mouse (Apodemus epimelas); 513. Hyrcanian Field Mouse (Apodemus hyrcanicus); 514. Caucasus Field Mouse (Apodemus ponticus); 515. Herb Field Mouse (Apodemus uralensis); 516. Yellow-necked Field Mouse (Apodemus flavicollis); 517. Eastern Broad-toothed Field Mouse (Apodemus mystacinus), 518. Steppe Field Mouse (Apodemus witherbyi); 519. Nepalese Field Mouse (Apodemus gurkha); 520. Himalayan Field Mouse (Apodemus pallipes); 521. Kashmir Field Mouse (Apodemus rusiges); 522. Chevrier's Field Mouse (Apodemus chevrieri); 523. South China Field Mouse (Apodemus draco); 524. Large-eared Field Mouse (Apodemus latronum); 525. Taiwan Field Mouse (Apodemus semotus); 526. Korean Field Mouse (Apodemus peninsulae); 527. Small Japanese Field Mouse (Apodemus argenteus); 528. Large Japanese Field Mouse (Apodemus speciosus); 529. Okinawa Island Spiny Rat (Tokudaia muenninki); 530. Amami Spiny Rat (Tokudaiaosimensis); 531. Tokunoshima Spiny Rat (Tokudaia tokunoshimensis). in Muridae
On following pages: 507. Cansdale's Swamp Rat (Malacomys cansdalel); 508. Edwards's Swamp Rat (Malacomys edwards); 509. Alpine Field Mouse (Apodemus alpicola), 510. Long-tailed Field Mouse (Apodemus sylvaticus); 511. Striped Field Mouse (Apodemus agrarius); 512. Western Broad-toothed Field Mouse (Apodemus epimelas); 513. Hyrcanian Field Mouse (Apodemus hyrcanicus); 514. Caucasus Field Mouse (Apodemus ponticus); 515. Herb Field Mouse (Apodemus uralensis); 516. Yellow-necked Field Mouse (Apodemus flavicollis); 517. Eastern Broad-toothed Field Mouse (Apodemus mystacinus), 518. Steppe Field Mouse (Apodemus witherbyi); 519. Nepalese Field Mouse (Apodemus gurkha); 520. Himalayan Field Mouse (Apodemus pallipes); 521. Kashmir Field Mouse (Apodemus rusiges); 522. Chevrier's Field Mouse (Apodemus chevrieri); 523. South China Field Mouse (Apodemus draco); 524. Large-eared Field Mouse (Apodemus latronum); 525. Taiwan Field Mouse (Apodemus semotus); 526. Korean Field Mouse (Apodemus peninsulae); 527. Small Japanese Field Mouse (Apodemus argenteus); 528. Large Japanese Field Mouse (Apodemus speciosus); 529. Okinawa Island Spiny Rat (Tokudaia muenninki); 530. Amami Spiny Rat (Tokudaiaosimensis); 531. Tokunoshima Spiny Rat (Tokudaia tokunoshimensis).
Data for figures in the manuscript "Refraction of the M2 internal tides induced by mesoscale eddies in the South China Sea"
<p>Data for figures in the manuscript "Refraction of the M2 internal tides induced by mesoscale eddies in the South China Sea"</p>
Data along sections in the South China Sea
<p>This is the latest version of the data that are used for reproducing the results of the paper by Dong et al. (2022) entitled "Turbulent dissipation in the surface mixed layer of an anticyclonic mesoscale eddy in the South China Sea".</p>
Figure 5 in Three new species of free-living marine nematodes from the central basin of the South China Sea
Figure 5. Setoplectus minor sp. nov. (a) Pharyngeal region of male, showing cephalic setae, amphid, and pharyngeal bulbs; (b) posterior region of male, showing spicule, gubernaculum and precloacal supplement; (c) anterior end of male, showing cephalic setae, buccal cavity and amphid; (d) entire female, showing amphid, pharyngeal bulb and reproductive system. Scale bars: a, b, c = 10 µm; d = 20 µm.
Figure 4 in Three new species of free-living marine nematodes from the central basin of the South China Sea
Figure 4. Minolaimus distalamphidus sp. nov. (a, b) Anterior end of male, showing anterior sensilla and amphidial fovea; (c) cuticle in the middle of body, showing lateral differentiation; (d) cloacal region of male, showing spicule, gubernaculum and precloacal supplements; (e) posterior part of body. Scale bars: a, b, d = 20 µm; c = 10 µm; e = 50 µm.
Figure 6 in Three new species of free-living marine nematodes from the central basin of the South China Sea
Figure 6. Setoplectus minor sp. nov. (a) Pharyngeal region of male, showing cephalic setae (arrow); (b) pharyngeal region of male, showing pharyngeal bulb and amphid (arrow); (c) cloacal region of male, showing spicule, gubernaculum and precloacal supplement; (d) entire female, showing amphid (arrow 1), pharyngeal bulb and valve (arrow 2). Scale bars: a, b, c = 10 µm; d = 20 µm.
Figure 3 in Three new species of free-living marine nematodes from the central basin of the South China Sea
Figure 3. Minolaimus distalamphidus sp. nov. (a) Anterior region of male, showing amphid and lateral differentiation; (b) pharyngeal region; (c) posterior region, showing tail; (d) cloacal region, showing spicule, gubernaculum and precloacal supplements. Scale bars: 20 µm.
Figure 2 in Three new species of free-living marine nematodes from the central basin of the South China Sea
Figure 2. Elzalia longicaudata sp. nov. (a) Lateral view of male pharyngeal region, showing amphid; (b) anterior end of male, showing buccal cavity, cephalic setae and cervical setae; (c) male tail; (d) cloacal region of male, showing spicules; (e) cloacal region of male, showing gubernaculum. Scale bars: a, c, d = 20 µm; b, e = 10 µm.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.