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.
137
datasets available to search
ShareScore release 0.9.0
Dataset results
137 results for “worldwide distribution”
Distribution. Worldwide in tropical and subtropical waters from c.40° N to ¢.35° §, including the Gulf of Mexico, Arabian Sea, Bay of Bengal, South China Sea, and Timor Sea. in Delphinidae
Distribution. Worldwide in tropical and subtropical waters from c.40° N to ¢.35° §, including the Gulf of Mexico, Arabian Sea, Bay of Bengal, South China Sea, and Timor Sea.
Distribution. Worldwide in tropical and warm temperate oceanic waters mainly from ¢.50° N to ¢.50° S, including semi-enclosed seas such as Gulf of California, Gulf of Mexico, Mediterranean Sea, Arabian Sea, Red Sea, Sea ofJapan, and Yellow Sea. in Delphinidae
Distribution. Worldwide in tropical and warm temperate oceanic waters mainly from ¢.50° N to ¢.50° S, including semi-enclosed seas such as Gulf of California, Gulf of Mexico, Mediterranean Sea, Arabian Sea, Red Sea, Sea ofJapan, and Yellow Sea.
Subspecies and Distribution. 1. t. truncatus Montagu, 1821 — worldwide in temperate and tropical waters as far S as New Zealand and generally as far as 45° N, but reaching the Faroe Is in the N Atlantic. 1: 1. ponticus Barabash-Nikiforov, 1940 — inhabits the Black Sea, Kerch Strait along with the connecting part of the Azov Sea, and the Turkish Straits system. in Delphinidae
Subspecies and Distribution. 1. t. truncatus Montagu, 1821 — worldwide in temperate and tropical waters as far S as New Zealand and generally as far as 45° N, but reaching the Faroe Is in the N Atlantic. 1: 1. ponticus Barabash-Nikiforov, 1940 — inhabits the Black Sea, Kerch Strait along with the connecting part of the Azov Sea, and the Turkish Straits system.
Distribution. Worldwide in tropical to temperate tropical to temperate oceanic waters between ¢.60° N and 60° S including the North Sea, Mediterranean Sea, and northern Gulf of Alaska. in Delphinidae
Distribution. Worldwide in tropical to temperate tropical to temperate oceanic waters between ¢.60° N and 60° S including the North Sea, Mediterranean Sea, and northern Gulf of Alaska.
Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms. in Leporidae
Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms.
Distribution. Originally native to the Indian Subcontinent and now introduced worldwide, including the sub-Antarctic Macquarie I but not Antarctica (modern introductions not shaded on the map). in Muridae
Distribution. Originally native to the Indian Subcontinent and now introduced worldwide, including the sub-Antarctic Macquarie I but not Antarctica (modern introductions not shaded on the map).
Distribution. Originally native to N China (possibly Mongolia), SW Siberia in Russia, and Japan, and now introduced worldwide, except Antarctica (modern introductions not shaded on the map). in Muridae
Distribution. Originally native to N China (possibly Mongolia), SW Siberia in Russia, and Japan, and now introduced worldwide, except Antarctica (modern introductions not shaded on the map).
Subspecies and Distribution. M.m.musculusLinnaeus,1758—EEurope,CAsia,andChina. M.m.castaneusWaterhouse,1843—Kenya,Madagascar,Pakistan,India,andSEAsia. M. m. domesticus E. Schwarz & H. K. Schwarz, 1943 — W Europe and N Africa. M. m. gentilulus Thomas, 1919 — Arabian Peninsula. Also three unnamed geographic lineages from C & SE Iran and Nepal. Now introduced worldwide, except Antarctica (modern introductions not shaded on the map). in Muridae
Subspecies and Distribution. M.m.musculusLinnaeus,1758—EEurope,CAsia,andChina. M.m.castaneusWaterhouse,1843—Kenya,Madagascar,Pakistan,India,andSEAsia. M. m. domesticus E. Schwarz & H. K. Schwarz, 1943 — W Europe and N Africa. M. m. gentilulus Thomas, 1919 — Arabian Peninsula. Also three unnamed geographic lineages from C & SE Iran and Nepal. Now introduced worldwide, except Antarctica (modern introductions not shaded on the map).
A species distribution model of the giant kelp Macrocystis pyrifera: Worldwide changes and a focus on the Southeast Pacific
<p>Worldwide climate-driven shifts in the distribution of species is of special concern when it involves habitat-forming species. In the coastal environment, large Laminarian algae—kelps—form key coastal ecosystems that support complex and diverse food webs. Among kelps, <em>Macrocystis pyrifera</em> is the most widely distributed habitat-formingspecies and provides essential ecosystem services. This study aimed to establish the main drivers of future distributional changes on a global scale and use them to predict future habitat suitability. Using species distribution models (SDM), we examined the changes in global distribution of <em>M. pyrifera</em> under different emission scenarios with a focus on the Southeast Pacific shores. To constrain the drivers of our simulations to the most important factors controlling kelp forest distribution across spatial scales, we explored a suite of environmental variables and validated the predictions derived from the SDMs. Minimum sea surface temperature was the single most important variable explaining the global distribution of suitable habitat for <em>M. pyrifera</em>. Under different climate change scenarios, we always observed a decrease of suitable habitat at low latitudes, while an increase was detected in other regions, mostly at high latitudes. Along the Southeast Pacific, we observed an upper range contraction of −17.08° S of latitude for 2090–2100 under the RCP8.5 scenario, implying a loss of habitat suitability throughout the coast of Peru and poleward to −27.83° S in Chile. Along the area of Northern Chile where a complete habitat loss is predicted by our model, natural stands are under heavy exploitation. The loss of habitat suitability will take place worldwide: Significant impacts on marine biodiversity and ecosystem functioning are likely. Furthermore, changes in habitat suitability are a harbinger of massive impacts in the socio-ecological systems of the Southeast Pacific.</p>
Figure 2 in Worldwide distribution of Syllophopsis subcoeca (Hymenoptera: Formicidae), an Old-World species long known only from the West Indies
Figure 2. Syllophopsis subcoeca worker from Tortola, British Virgin Islands (collected by J.K. Wetterer; photo by M. Esposito; from www.antweb.org; CASENT0923381).
Figure 3 in Worldwide distribution of Syllophopsis subcoeca (Hymenoptera: Formicidae), an Old-World species long known only from the West Indies
Figure 3. Distribution records of Syllophopsis subcoeca in the West Indies and Florida (from www. antweb.org).
FIGURE 28 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 28. Emertonia berndi sp. nov. Female (holotype). A, P5 (holotype); B, P6 and genital field. Scale bar = 0.02 mm.
FIGURE 27 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 27. Emertonia berndi sp. nov. Female (holotype). A, P1; B, P2 with intercoxal sclerite; C, P3; D, P4. Scale bar = 0.02 mm.
FIGURE 26 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 26. Emertonia berndi sp. nov. Female. A, antenna (paratype 1); B, mandibular palp (paratype 3); C, maxillule, disarticulated (paratype 2); D, maxilla (paratype 2); E, maxilliped (paratype 1). Scale bar = 0.01 mm.
FIGURE 25 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 25. Emertonia berndi sp. nov. Female (holotype). A, antennule (armature omitted); B, disarticulated antennulary segments showing armature. Scale bar = 0.02 mm.
FIGURE 24 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 24. Emertonia berndi sp. nov. Female (holotype). A, habitus, dorsal view; B, habitus, lateral view; C, caudal ramus, dorsal view. Scale bars = a, b, 0.1 mm; c, 0.02 mm.
FIGURE 23 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 23. Emertonia hessleri sp. nov. Male (paratype 3). A, right antennule, ventral view; B, left antennule (not all segments illustrated). Scale bar = 0.02 mm.
FIGURE 22 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 22. Emertonia hessleri sp. nov. Male (allotype). A, habitus, dorsal view; B, habitus, lateral view; C, caudal ramus, dorsal view. Scale bars = a, b, 0.05 mm; c, 0.02 mm.
FIGURE 16 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 16. Emertonia ilse sp. nov. Male (paratype 1). A, antennule (armature omitted); B, disarticulated antennulary segments showing armature. Scale bar = 0.02 mm.
FIGURE 19 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 19. Emertonia hessleri sp. nov. Female. A, antenna (paratype 4); B, mandibular palp (paratype 2); C, maxillule, disarticulated (paratype 2); D, maxilla (paratype 4); E, maxilliped (paratype 4). Scale bar = 0.01 mm.
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.