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.
736
datasets available to search
ShareScore release 0.9.0
Dataset results
736 results for “East China”
Figure 3 in First record of the East Asian fourfinger threadfin, Eleutheronema rhadinum (Jordan & Evermann, 1902), from Zhenjiang, China
Figure 3. – Head of Eleutheronema rhadinum, showing anterior two-thirds of lower jaw with small teeth extending onto lateral surface, adjacent portion of lip absent. JSFFRI-18010, 219.6 mm SL.
Figs 6 – 12 in New data on the subgenus Callophrys (Ahlbergia) (Lepidoptera: Lycaenidae) from East Asia, with description of a new species from China and confirmation of the record of C. (A.) ferrea from Russia
Figs 6 – 12. Callophrys (Ahlbergia) spp., genitalia. 6-9 – C. (A.) abae sp. n.: 6 – holotype, ♂, genital capsule with valvae, ventral view; 7 – Id., aedeagus, lateral view; 8 – Id., vesica of aedeagus with cornuti; 9 – paratype, ♀, China, Sichuan Province, Ngawa Tibetan and Qiang Autonomous Prefecture, Songpan County, 2900 m and higher, 24.VI.1894, M.M. Berezovsky leg., lamella postvaginalis, antrum, ductus bursae and bursa, ventral view; 10-12 – C. (A.) ferrea (Butler, 1866): 10 – ♂, Russia, Kunashir Island, 4.5 km NW Mendeleevo airport, Tretyakovo village, 19.V 2021, S. Rybalkin leg., genital capsule with valvae, ventral view; 11 – Id., aedeagus, lateral view; 12 – Id., vesica of aedeagus with cornuti.
Figs 1–5 in New data on the subgenus Callophrys (Ahlbergia) (Lepidoptera: Lycaenidae) from East Asia, with description of a new species from China and confirmation of the record of C. (A.) ferrea from Russia
Figs 1–5. Callophrys (Ahlbergia) abae sp. n., adults, dorsal view (above), ventral view (below) and corresponding labels. 1 – holotype, ♂ (ZISP); 2 – labels of the holotype; 3 – paratype, ♂, voucher No. CAL075, GenBank accession No. OM630563, China, Sichuan Province, Ngawa Tibetan and Qiang Autonomous Prefecture, Jinchuan County, Jinchuan env., 1900 m, 07.VI.2015, V. Patrikeev leg. (VTM); 4 – paratype, ♀, [China, Sichuan Province, Ngawa Tibetan and Qiang Autonomous Prefecture, Songpan County / 9500 ft. [2900 m] [above sea level] and higher / M.M. Berezovsky leg. 24.VI.1894] (ZISP); 5 – labels of previous specimen. 24
Fig. 2 in Invertebrate Fauna Associated with Floating Sargassum horneri (Fucales: Sargassaceae) in the East China Sea
Fig. 2. Density of total taxa of epibionts on floating algae (A), abundance of total taxa (B), and Simpson's diversity index (C) presented as box plots. The number above each box indicates the number of examined algal rafts per station. The black line in each box shows the median and the whiskers show the range except for the outlier (black dot).
Fig. 3 in Invertebrate Fauna Associated with Floating Sargassum horneri (Fucales: Sargassaceae) in the East China Sea
Fig. 3. Correlations between number of total taxa and examined algal wet weight (A) (n=53, R2=0.21); abundance of total taxa and examined algal wet weight (B) (n=53, R2=0.41); and Simpson's diversity index and examined algal wet weight (C) (n=53, R2 = 0.10).
Stable Water Isotopes and Nutrients in the Changjiang (Yangtze River) Estuary and adjacent East China Sea shelf in Winter
<p>The dataset presented here includes the temperature, salinity, stable water isotopes, and nutrients of seawater from the Changjiang Estuary and adjacent East China Sea shelf in March 2013. </p>
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021). in Floristic, Vegetation And Climate Assessment Of The Early/Middle Miocene Parschlug Flora Indicates A Distinctly Seasonal Climate
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021).
Text-fig. 4. Graphical visualization of Phytogeographic Reference Regions Assessment (PRRA) of nearest living relative genera of fossil-taxa from late Early Miocene Wiesa assemblage in eastern Germany. Analysis yields only NLRs which have modern distribution area (partly) in E and SE Asia. For relationships of fossil-taxa to nearest living relatives or ecological equivalents, see Tab. 6; taxa used for analysis marked with asterisks. Three geographic resolutions conducted: a – grid with 1.5° latitude/longitude resolution, b – grid with 2°, c – grid with 3°; similarity column indicates cooccurrences of genera of nearest living relatives in single grid box. Maximum value in our analysis: grid box marked with arrow in map a, located in western Yunnan Province, P. R. China and southern Kachin Province, NE Myanmar (east of Myitkyina city), area with 97.371 7–98.874 2° longitude and 24.586 7–25.837 5° latitude, yields 23 co-occurring species of 13 genera (Tab. 7). in Assessment Of Phytogeographic Reference Regions For Cenozoic Vegetation: A Case Study On The Miocene Flora Of Wiesa (Germany)
Text-fig. 4. Graphical visualization of Phytogeographic Reference Regions Assessment (PRRA) of nearest living relative genera of fossil-taxa from late Early Miocene Wiesa assemblage in eastern Germany. Analysis yields only NLRs which have modern distribution area (partly) in E and SE Asia. For relationships of fossil-taxa to nearest living relatives or ecological equivalents, see Tab. 6; taxa used for analysis marked with asterisks. Three geographic resolutions conducted: a – grid with 1.5° latitude/longitude resolution, b – grid with 2°, c – grid with 3°; similarity column indicates cooccurrences of genera of nearest living relatives in single grid box. Maximum value in our analysis: grid box marked with arrow in map a, located in western Yunnan Province, P. R. China and southern Kachin Province, NE Myanmar (east of Myitkyina city), area with 97.371 7–98.874 2° longitude and 24.586 7–25.837 5° latitude, yields 23 co-occurring species of 13 genera (Tab. 7).
Figure 4. Diagrammaticfigureofajuvenileof Zenopsis stabilispinosa, AMS I.31147-002 in A new species of Zenopsis (Zeiformes: Zeidae) from the South China Sea, East China Sea and off Western Australia
Figure 4. Diagrammaticfigureofajuvenileof Zenopsis stabilispinosa, AMS I.31147-002 (80.4 mm SL), paratype.
Figure 3 in A new species of Zenopsis (Zeiformes: Zeidae) from the South China Sea, East China Sea and off Western Australia
Figure 3. Diagrammatic figures of anal-fin pterygiophores and spines of 3 species of Zenopsis: A, Z. stabilispinosa, holotype, FAKU 64803 (307.2 mm SL); B, Z. nebulosa, FAKU 64805 (379 mm SL); C, Z. conchifer, RUSI 14070 (135.5 mm SL). Scales indicate 10 mm.
Figure 2 in A new species of Zenopsis (Zeiformes: Zeidae) from the South China Sea, East China Sea and off Western Australia
Figure 2. Diagrammatic figure (A), and teeth on jaws and vomer (B) of the holotype of Zenopsis stabilispinosa sp. nov., FAKU 64803.
Figs 54–57 in Millipedes (Diplopoda) From Korea, The Russian Far East, And China In The Collection Of The Hungarian Natural History Museum
Figs 54–57. Koreadesmus proprius gen. sp. n.: 54–57 = gonopod, mesal, frontal,lateral and caudal view, r – postfemoral process, d – postfemoral tooth, t – flattened outgrowth of postfemorite, lo –
Figs 42–44 in Millipedes (Diplopoda) From Korea, The Russian Far East, And China In The Collection Of The Hungarian Natural History Museum
Figs 42–44. Ansiulus aberrans sp. n.: 42 = antenna, 43 = legpair 1, caudal view, 44 = legpair 2 and penes, caudal view. Scales in mm
Figs 50–53 in Millipedes (Diplopoda) From Korea, The Russian Far East, And China In The Collection Of The Hungarian Natural History Museum
Figs 50–53. Koreadesmus proprius gen. sp. n.: 50 = antenna, 51–52 = somite 10, dorsal and lateral view, 53 = lamina between coxae 4. Scales in mm
Figs 45–49 in Millipedes (Diplopoda) From Korea, The Russian Far East, And China In The Collection Of The Hungarian Natural History Museum
Figs 45–49. Ansiulus aberrans sp. n.: 45 = legpair 7, frontal view, m from Ryanggang Prov., 46 = legpair 7, frontal view, m from North Pyongan Prov., 47 = anterior gonopod, caudomesal view, 48 = posterior gonopod, lateral view, m from Ryanggang Prov., 49 = posterior gonopod, lateral view, m
Fig. 41 in Millipedes (Diplopoda) From Korea, The Russian Far East, And China In The Collection Of The Hungarian Natural History Museum
Fig. 41. Scatterplot of vertical diameter of somite 23 to number of podous somites in various populations of Anaulaciulus golovatchi MIKHALJOVA, 1982. o = males from Russian Far East; n = males
Figs 14–18 in Millipedes (Diplopoda) From Korea, The Russian Far East, And China In The Collection Of The Hungarian Natural History Museum
Figs 14–18. Skleroprotopus costatus sp. n.: 14 = antenna, 15 = legpair 1, frontal view, 16 = terminal segment of legpair 1, ventral view, 17 = penes, caudal view, 18 = legpair 7, frontal view. Scales in mm
Figs 29–40. Anaulaciulus golovatchi MIKHALJOVA, 1982 in Millipedes (Diplopoda) From Korea, The Russian Far East, And China In The Collection Of The Hungarian Natural History Museum
Figs 29–40. Anaulaciulus golovatchi MIKHALJOVA, 1982, variation in shape of opisthomerite apex: 31, 32, 33, 34, 37 = mm from North Korea, 29, 30, 39 = mm from Russian Far East, Primorsky kray, Ussuriysky Nature Reserve, 35 = m from Russian Far East, Primorsky kray, Lazovsky Nature Reserve, 36, 38 = mm from Russian Far East, Primorsky kray, "Kedrovaya Pad" Nature Reserve, 40 = m
Figs 6–13 in Millipedes (Diplopoda) From Korea, The Russian Far East, And China In The Collection Of The Hungarian Natural History Museum
Figs 6–13. Skleroprotopus chollus sp. n.: 6 = gnathochilarium, 7 = antenna, 8 = legpair 1, lateral view, 9 = legpair 2 and penes, caudal view, 10 = legpair 7, frontal view, 11 = telopodite remnant of legpair 7 (enlarged not to scale), 12 = anterior gonopod, caudal view, 13 = posterior gonopod, mesal
Figs 26–28 in Millipedes (Diplopoda) From Korea, The Russian Far East, And China In The Collection Of The Hungarian Natural History Museum
Figs 26–28. Skleroprotopus ramuliferus LIM et MIKHALJOVA, 2001: 26 = legpair 7, caudal view, m paratype from South Korea, 27–28 = distal part of posterior gonopod, lateral view, m from North Ko-
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.