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.
28,952
datasets available to search
ShareScore release 0.7.1
Dataset results
28,952 results for “Distributed”
Fig. 4 in Observations On Species Abundance Distribution In Fly Collections
Fig. 4. Further frequency polygons of 2-moving averaged frequencies. A, B and C refer to artificial collections mentioned in the text. Details see at Fig. 1.
Fig. 2 in Observations On Species Abundance Distribution In Fly Collections
Fig. 2. Frequency polygons of 2-moving averaged frequencies relating to combined collections. The 2003–2004 polygon is shifted in the figure by two abundance classes to the right. Details see at Fig. 1.
Figure. 1 in Stoneflies (Plecoptera) of the Czech Republic: species checklist, distribution and protection status
Figure. 1. Map of the Czech Republic showing 8 districts based on main river basins. Published data are marked by circle, new unpublished data by × mark. Main mountains are marked by numbers, their Czech, English and German names are listed: 1 – Doupovské hory (Duppauer Gebirge) Mts., 2 – Slavkovský les Mts., 3 – Krušné hory (Ore/Erzgebirge) Mts., 4 – Jizerské hory (Isergebirge) Mts., 5 – Krkonoše (Giant/Riesengebirge) Mts., 6 – Orlické hory (Adlergebirge) Mts., 7 – Kralický Sněžník Mt.; 8 – Hrubý Jeseník (Altvatergebirge/Hohes Gesenke) Mts., 9 – Šumava (Bohemian Forest/Böhmerwald) Mts., 10 – Novohradské hory Mts., 11 – Českomoravská vrchovina (Böhmisch-Mährische Höhe), 12 – Moravskoslezské Beskydy Mts., 13 – Bílé Karpaty Mts.
Fig. 2 in New Distributional Records of Three Species of Euphylliidae (Cnidaria, Anthozoa, Hexacorallia, Scleractinia) from the Ryukyu Islands, Japan
Fig. 2. Corallum of Fimbriaphyllia species currently reported from the Ryukyu Islands, Japan, F. paraancora (A–D) and F. paradivisa (E–H). A, KAUM-CN-10, Tean, Amami-Oshima island, Kagoshima, Japan, depth of 32 m; B, CMNH-ZG09105, Tean, Amami-Oshima island, Kagoshima, Japan, depth of 35 m; C, CMNH-ZG 08523, Wase, Amami-Oshima island, Kagoshima, Japan, depth of 9 m; D, CMNH- ZG 07195, Ii-nanshi, Ogamijima island, Okinawa, Japan, depth of 10 m; E, KAUM-CN-11, Tean, Amami-Oshima island, Kagoshima, Japan, depth of 32 m; F, CMNH-ZG 09661, Tean, Amami-Oshima island, Kagoshima, Japan, depth of 32 m; G, KAUM-CN-12, Henoko, Okinawajima island, Okinawa, Japan, depth of 28 m; H, CMNH-ZG-09661, Henoko, Okinawajima island, Japan, depth of 28 m.
Fig. 1 in New Distributional Records of Three Species of Euphylliidae (Cnidaria, Anthozoa, Hexacorallia, Scleractinia) from the Ryukyu Islands, Japan
Fig. 1. Underwater appearance of living corals. A, in situ photograph of the colonies of Fimbriaphyllia paraancora (KAUM-CN-10) on the left and F.paradivisa (KAUM-CN-11) at Tean, Amami-Oshima island, Kagoshima, Japan, on 21 December 2017; B, an aggregation of F.paradivisa approximately 3–5 m in diameters on the muddy bottom in the usually turbid inner bay at a depth 28 m, Henoko, Okinawajima island, Okinawa, Japan, on 25 November 2010; C, extended polyps of F. paradivisa showing branching tentacles with spherical ends; D, extended polyps of F. paraancora showing tentacles with anchor-shaped tips; E, in situ photograph of Catalaphyllia jardinei (KAUM-CN-14) at Tean, Amami-Oshima island, Kagoshima, Japan, on 21 December 2017; F, polyps of C. jardinei showing small bubble-shaped tentacles at the edge of the oral disc.
Fig. 4 in New Distributional Records of Three Species of Euphylliidae (Cnidaria, Anthozoa, Hexacorallia, Scleractinia) from the Ryukyu Islands, Japan
Fig. 4. Specimens of Catalaphyllia jardinei preserved in the Smithsonian National Museum of Natural History (Photographs taken by Allison Becker) (USNM). A–B, corallite of USNM 1259568, collected at 52–55 m deep off Manza Horshoe Cliffs, Onna, Okinawajima island, Okinawa, Japan, on 21 December 1988, by Robert F. Bolland; C–D, corallite of USNM 94409, collected at 27 m deep off Nago City, Nago, Okinawajima island, Okinawa, Japan, on 21 February 1992, by R. F. Bolland.
Fig. 3 in New Distributional Records of Three Species of Euphylliidae (Cnidaria, Anthozoa, Hexacorallia, Scleractinia) from the Ryukyu Islands, Japan
Fig. 3. Corallum of Catalaphyllia jardinei currently reported from Amami-Oshima island, Japan. A, side view of the corallite of KAUM- CN-14; B, view from the top side of the corallite and the calice of KAUM-CN-14; C, side view of the corallite of CMNH-ZG 09662; D, view from the top side of the corallite and the calice of CMNH-ZG 0966 showing three-forked branching of the calice.
Fig. 3 in Salmincola edwardsii (Copepoda: Lernaeopodidae) Parasitic on Southern Asian Dolly Varden, Salvelinus malma krascheninnikova, from Hokkaido Island, Japan, with the Southernmost Distribution Record of the Copepod in Asia
Fig. 3. Map of Hokkaido Island and the southern Kuril Islands, showing the collection localities of Salmincola edwardsii in the previous (closed triangles, Shedko and Shedko, 2002) and present (closed circles) studies. Open circles show no copepod infection on southern Asian Dolly Varden. 1, Olya Inlet (Prostor Bay), Iturup Island; 2, Kuibyshev Bay, Iturup Island; 3, Petrova River, Kunashir Island; 4, a nameless creek, Kunashir Island; 5, Rusha River; 6, Rausu River; 7, Shari River; 8, Shibetsu River; 9, Saru River; 10, Yoichi River; 11, Shiribetsu River; 12, Notto River; 13, Chihase River.
Fig. 2 in Salmincola edwardsii (Copepoda: Lernaeopodidae) Parasitic on Southern Asian Dolly Varden, Salvelinus malma krascheninnikova, from Hokkaido Island, Japan, with the Southernmost Distribution Record of the Copepod in Asia
Fig. 2. Female of Salmincola edwardsii attached to the base of gill filament of southern Asian Dolly Varden, Salvelinus malma krascheninnikova, from the Shari River, Hokkaido Island. Formalinfixed and later ethanol-preserved specimen, lateral view. Abbreviations: c, cephalothorax; es, egg sac; ga, gill arch; gf, gill filament; mx2, second maxilla; mxp, maxilliped; t, trunk. Scale bar: 1 mm. Note most portions of the infected gill filament lost, and a bulbous swelling (*) enveloping the bulla.
Fig. 1 in Salmincola edwardsii (Copepoda: Lernaeopodidae) Parasitic on Southern Asian Dolly Varden, Salvelinus malma krascheninnikova, from Hokkaido Island, Japan, with the Southernmost Distribution Record of the Copepod in Asia
Fig. 1. Salmincola edwardsii, female, from southern Asian Dolly Varden, Salvelinus malma krascheninnikova, from the Shari River, Hokkaido Island. A, habitus, anterolateral view; B, second antenna, lateral view; C, mandible, lateral view; D, first maxilla, lateral view; E, maxilliped, lateral view. Abbreviations: ant2, second antenna; b, bulla; c, cephalothorax; es, egg sac; ex, exopod; h1, hook 1; mx2, second maxilla; mxp, maxilliped; p, palp; p4, process 4; p5, process 5; s2, spine 2; sy, sympod; t, trunk. Scale bars: A, 1 mm; B, 50 µm; C, 20 µm; D, 100 µm; E, 200 µm.
Fig. 1 in New Record of a Marine Fish Parasite Nerocila trichiura (Crustacea: Isopoda: Cymothoidae) from Japan, with its Confirmed Distribution in the Western North Pacific Ocean
Fig. 1. Nerocila trichiura, ovigerous female, NSMT-Cr 26315. A, Cypselurus hiraii (252 mm in total length) infested with N. trichiura (arrow); B, skin wound at attachment site; C, N. trichiura, dorsal view, fresh specimen. Scale bars: A, 50 mm; B, C, 10 mm.
Fig. 2 in New Record of a Marine Fish Parasite Nerocila trichiura (Crustacea: Isopoda: Cymothoidae) from Japan, with its Confirmed Distribution in the Western North Pacific Ocean
Fig. 2. Nerocila trichiura, ovigerous female, NSMT-Cr 26315. A, dorsal view; B, lateral view; C, cephalon and pereonite 1, dorsal view; D, pleotelson and right uropod, dorsal view; E, pereopod 7. Scale bars: A, B, 10 mm; C, E, 2 mm; D, 5 mm.
Fig. 3 in New Record of a Marine Fish Parasite Nerocila trichiura (Crustacea: Isopoda: Cymothoidae) from Japan, with its Confirmed Distribution in the Western North Pacific Ocean
Fig. 3. Map showing the localities where Nerocila trichiura was collected in the previous (circles) and present (star) studies. 1, 31°N, 76°W (Schioedte and Meinert 1881); 2, the West Indies (Trilles 1979); 3, Dakar Harbor, Senegal (Bruce and Harrison-Nelson 1988); 4, Banana and an unknown locality, Congo (Nierstrasz 1918; Monod 1931); 5, Durban, South Africa (Barnard 1955; Kensley 1978); 6, Comoro Islands (Kensley 2001); 7, Mauritius (type locality, Mier 1877; Bruce and Harrison-Nelson 1988); 8, 10°20′S, 70°00′E (Bruce and Harrison-Nelson 1988); 9, Great Chagos (Stebbing 1910); 10, Tamil Nadu coast, India (Trilles et al. 2013; Rameshkumar et al. 2013); 11, Zamboanga, Philippines (Schioedte and Meinert 1881); and 12, Kowaura Bay, Japan (this paper).
FIG. 4 in Presence of the foraminifer Chapmanina gassinensis Silvestri, 1931, in the Eocene (Lutetian) of the Grignon "falunière" (Yvelines, Paris Basin). The genus Chapmanina, its species and world distribution
FIG. 4. — Distribution of Chapmanina gassinensis Silvestri,1931 in the Oligocene of Europe. The numbers correspond to the references indicated in the Appendix 1.
FIG. 5 in Presence of the foraminifer Chapmanina gassinensis Silvestri, 1931, in the Eocene (Lutetian) of the Grignon "falunière" (Yvelines, Paris Basin). The genus Chapmanina, its species and world distribution
FIG. 5. — Distribution of Chapmanina Silvestri, 1931 in the Eocene of Asia. The numbers correspond to the references indicated in the Appendix 1.
FIG. 3 in Presence of the foraminifer Chapmanina gassinensis Silvestri, 1931, in the Eocene (Lutetian) of the Grignon "falunière" (Yvelines, Paris Basin). The genus Chapmanina, its species and world distribution
FIG. 3. — Distribution of Chapmanina gassinensis Silvestri, 1931 in the Eocene of Europe and North Africa. The numbers correspond to the references indicated in the Appendix 1.
FIG. 2 in Presence of the foraminifer Chapmanina gassinensis Silvestri, 1931, in the Eocene (Lutetian) of the Grignon "falunière" (Yvelines, Paris Basin). The genus Chapmanina, its species and world distribution
FIG. 2. — The "Falunière" of Grignon section, after Guernet et al. (2012) for the section profile, lithologic units and sub-units and descriptions, Gély (1996) for the sequential units and Huyghe et al. (2012) for the correlation of sequential and lithologic units. Section profile modified from Sanders et al. 2015.
FIG. 1 in Presence of the foraminifer Chapmanina gassinensis Silvestri, 1931, in the Eocene (Lutetian) of the Grignon "falunière" (Yvelines, Paris Basin). The genus Chapmanina, its species and world distribution
FIG. 1. — Chapmanina gassinensis Silvestri, 1931 (Lutetian, Grignon falunière, Yvelines), in lateral (A) and apical (B) views (MNHN.F.F62410). Scale bars: 200 µm.
Fig. 4 in Distribution and reproductive biology of the Electric ray Discopyge tschudii Heckel, 1846 in San Matías Gulf, Northern Patagonia, Argentina
Fig. 4. Size frequency distribution of Discopyge tschudii sampled during 2004-2007. Males (dotted line) n= 564 and females (continuous line) n= 523.
Fig. 9 in Distribution and reproductive biology of the Electric ray Discopyge tschudii Heckel, 1846 in San Matías Gulf, Northern Patagonia, Argentina
Fig. 9. Relationship between total length of the female (TL) and number of embryos (N e) for Discopyge tschudii. N e (dotted line)= 0.221 X exp(0.589 X TL); R²= 0.57; n= 27.
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.