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FIGURE 6 in Description of a new species of Priolepis (Perciformes: Gobiidae) from the Red Sea, a new record of Priolepis compita, and a distributional range extension of Trimma fishelsoni
FIGURE 6. Underwater photographs of alive individuals. A: Trimma fishelsoni, Dahab, Gulf of Aqaba, Red Sea; B: Trimma taylori, Al Lith, Saudi Arabia, Red Sea. Photos by S.V. Bogorodsky.
FIGURE 5. Trimma fishelsoni, SMF 35737 in Description of a new species of Priolepis (Perciformes: Gobiidae) from the Red Sea, a new record of Priolepis compita, and a distributional range extension of Trimma fishelsoni
FIGURE 5. Trimma fishelsoni, SMF 35737, cephalic sensory papillae of head. Dorsal (top), lateral (middle) and ventral (bottom) views of head. Dots represent the sensory papillae; AN= anterior nares, PN= posterior nares; arrows show position of lower end of gill opening. Photo and drawing by T. Suzuki.
FIGURE 2. Priolepis melanops n in Description of a new species of Priolepis (Perciformes: Gobiidae) from the Red Sea, a new record of Priolepis compita, and a distributional range extension of Trimma fishelsoni
FIGURE 2. Priolepis melanops n. sp., SMF 35728, holotype, cephalic sensory papillae of head. Dorsal (top), lateral (middle) and ventral (bottom) views of head. Dots represent the sensory papillae; AN= anterior nares, PN= posterior nares; arrow shows position of lower end of gill opening. Photo and drawing by T. Suzuki.
FIGURE 3. A in Description of a new species of Priolepis (Perciformes: Gobiidae) from the Red Sea, a new record of Priolepis compita, and a distributional range extension of Trimma fishelsoni
FIGURE 3. A: Priolepis compita, live individual, Sharm el Moya, at entrance of the Gulf of Aqaba, Red Sea; B: Priolepis semidoliata, fresh specimen, BPBM 41242, 21.0 mm SL, Dahab, Gulf of Aqaba, Red Sea. Photos by S.V. Bogorodsky.
FIGURE 1. Priolepis melanops, n in Description of a new species of Priolepis (Perciformes: Gobiidae) from the Red Sea, a new record of Priolepis compita, and a distributional range extension of Trimma fishelsoni
FIGURE 1. Priolepis melanops, n. sp., SMF 35728, holotype, female, 24.0 mm SL, Al Lith, Saudi Arabia, Red Sea A: freshly collected; B: preserved; C: ventral view of region between pelvic and anal fins; red line indicates basal membrane, yellow lines show fourth and fifth pelvic-fin rays. Photos by S.V. Bogorodsky (A) and T. Suzuki (B, C).
FIGURE 4. Trimma fishelsoni. A in Description of a new species of Priolepis (Perciformes: Gobiidae) from the Red Sea, a new record of Priolepis compita, and a distributional range extension of Trimma fishelsoni
FIGURE 4. Trimma fishelsoni. A: SMF 35735, fresh specimen, 20.0 mm SL, female, Al Lith, Saudi Arabia, Red Sea; B: SMF 35737, preserved specimen, 21.6 mm SL, male, Al Lith, Saudi Arabia, Red Sea. Photo by S.V. Bogorodsky (A) and T. Suzuki (B).
Construction of PROTAC-Mediated Ternary Complex Structure Distribution Profiles Using Extensive Conformational Search
<p>input files for MD simulations, the restart structures in the PaCS-MD and OFLOOD, and analysis scripts</p>
FIGURE 17 in Parrotfishes (Teleostei: Labridae: Scarini) of the Socotra Archipelago: Diversity and distributional biogeography, including a range extension of Scarus zufar Randall & Hoover, 1995
FIGURE 17. Double-Distributional Multigraph combining area-based (x-axis; Fig. S2-4) and species-based (y-axis; Fig. S2-8) resemblance patterns of 39 parrotfish species among 10 putative Arabian ecoregions (with separate checklists for the Eastern Gulf of Aden and Southern Oman) and 14 additional areas of the wider Western Indian Ocean across the distributional matrix (Supplement 1), columns and rows of which re-ordered according to the sequence arising from both dendrograms; also presenting 'richness-by-area' and 'presence-by-species' sums.
FIGURE 8. Scarus fuscopurpureus. A in Parrotfishes (Teleostei: Labridae: Scarini) of the Socotra Archipelago: Diversity and distributional biogeography, including a range extension of Scarus zufar Randall & Hoover, 1995
FIGURE 8. Scarus fuscopurpureus. A: initial phase, Di Hamri, Socotra Island, 2 m depth; B: terminal male, Ras Qatanahn, Socotra Island, 10 m depth.
FIGURE 9. Scarus ghobban. A in Parrotfishes (Teleostei: Labridae: Scarini) of the Socotra Archipelago: Diversity and distributional biogeography, including a range extension of Scarus zufar Randall & Hoover, 1995
FIGURE 9. Scarus ghobban. A: initial phase, Di Timri, Socotra Island, 12 m depth; B: initial phase, Di Hamri, Socotra Island, 10 m depth; C: terminal male, Ras Bidou, Socotra Island, 12 m depth.
FIGURE 3. Chlorurus strongylocephalus. A in Parrotfishes (Teleostei: Labridae: Scarini) of the Socotra Archipelago: Diversity and distributional biogeography, including a range extension of Scarus zufar Randall & Hoover, 1995
FIGURE 3. Chlorurus strongylocephalus. A: initial phase female, Di Hamri, Socotra Island, 4 m depth; B: initial phase male, Alameh, Socotra Island, 5 m depth; C: terminal male, Roosh, Socotra Island, 14 m depth.
FIGURE 16 in Parrotfishes (Teleostei: Labridae: Scarini) of the Socotra Archipelago: Diversity and distributional biogeography, including a range extension of Scarus zufar Randall & Hoover, 1995
FIGURE 16. Resemblance pattern of 10 putative Arabian ecoregions and Kenya (Scarini, 30 spp.) based on Hellinger distance, represented as plots of the (A) non-metric multidimensional scaling analysis (nMDS), overlaid with the cluster analysis and superposed with symbols representing the statistically (ANOSIM) best supported a priori-defined province-level combination X (Supplement 3); and the (B) hierarchical agglomerative cluster analysis according to separate checklists for the Eastern Gulf of Aden and Southern Oman.
FIGURE 7. Scarus frenatus. A in Parrotfishes (Teleostei: Labridae: Scarini) of the Socotra Archipelago: Diversity and distributional biogeography, including a range extension of Scarus zufar Randall & Hoover, 1995
FIGURE 7. Scarus frenatus. A: terminal male, Di Hamri, Socotra Island, 3 m depth; B: terminal male, Qariah, Socotra Island, 5 m depth.
FIGURE 11. Scarus rubroviolaceus. A in Parrotfishes (Teleostei: Labridae: Scarini) of the Socotra Archipelago: Diversity and distributional biogeography, including a range extension of Scarus zufar Randall & Hoover, 1995
FIGURE 11. Scarus rubroviolaceus. A: small initial phase, Roosh, Socotra Island, 3 m depth; B: initial phase, Di Hamri, Socotra Island, 10 m depth; C: terminal male, Abd al-Kuri Island, Socotra Archipelago, 8 m depth.
FIGURE 6. Scarus ferrugineus. A in Parrotfishes (Teleostei: Labridae: Scarini) of the Socotra Archipelago: Diversity and distributional biogeography, including a range extension of Scarus zufar Randall & Hoover, 1995
FIGURE 6. Scarus ferrugineus. A: terminal male, Di Hamri, Socotra Island, 5 m depth; B: terminal male, Roosh, Socotra Island, 14 m depth.
FIGURE 4. Scarus arabicus. A in Parrotfishes (Teleostei: Labridae: Scarini) of the Socotra Archipelago: Diversity and distributional biogeography, including a range extension of Scarus zufar Randall & Hoover, 1995
FIGURE 4. Scarus arabicus. A: initial phase, Abd al-Kuri Island, Socotra Archipelago, 7 m depth; B: SMF uncatalogued, initial phase, 26 cm SL, Hadibo fishmarket, Socotra Island; C: SMF uncatalogued, terminal male, 46 cm SL, Hadibo fishmarket, Socotra Island.
FIGURE 14. Scarus zufar. A in Parrotfishes (Teleostei: Labridae: Scarini) of the Socotra Archipelago: Diversity and distributional biogeography, including a range extension of Scarus zufar Randall & Hoover, 1995
FIGURE 14. Scarus zufar. A: initial phase, Eryssel, Socotra Island, 12 m depth; B: terminal male, Ras Bidou, Socotra Island, 14 m depth; C: terminal male, Eryssel, Socotra Island, 12 m depth.
Subspecies and Distribution. L. ¢c. capensis Linnaeus, 1758 — Western Cape Province (South Africa). L.c.aegyptiusDesmarest,1822—Egypt,Sudan,Palestine. L.c.aquiloThomas&Wroughton,1907—SMozambique. L. c. arabicus Hemprich & Ehrenberg, 1832 — Middle East, Arabian Peninsula, Iran, SW Pakistan (Baluchistan), and SW Afghanistan. . ¢. atlanticus de Winton, 1898 — Morocco. ¢. carpi Lundholm, 1955 — NW Namibia. granti Thomas & Schwann, 1904 — Northern Cape Province (South Africa). MDDnop hawker: Thomas, 1901 — W Sudan, Eritrea. isabellinus Cretzschmar, 1826 — Egypt, Sudan, Eritrea. Ean mediterraneus Wagner, 1841 — Sardinia. schlumberger: Remy Saint-Loup, 1894 — NE Morocco. sinaiticus Hemprich & Ehrenberg, 1832 — Egypt, Iraq. S whitakeri Thomas, 1902 — Libya, Niger and Algeria. The Cape Hare occurs in the Mediterranean I of Sardinia and in isolated populations scattered throughout most of the Arabian Peninsula and the Middle East and E to W Himalayas. This species has an extensive range in Africa which is separated in two distinct regions. First, in Egypt, Sudan, South Sudan, Eritrea, Ethiopia, Uganda, Kenya, and Tanzania, and throughout most of the dry savanna regions of C, W & N Africa, including parts of the Sahara Desert. Second, in savanna and semi-desert regions of Namibia, Botswana, S Zimbabwe, SW Mozambique, South Africa, Swaziland, and Lesotho. in Leporidae
Subspecies and Distribution. L. ¢c. capensis Linnaeus, 1758 — Western Cape Province (South Africa). L.c.aegyptiusDesmarest,1822—Egypt,Sudan,Palestine. L.c.aquiloThomas&Wroughton,1907—SMozambique. L. c. arabicus Hemprich & Ehrenberg, 1832 — Middle East, Arabian Peninsula, Iran, SW Pakistan (Baluchistan), and SW Afghanistan. . ¢. atlanticus de Winton, 1898 — Morocco. ¢. carpi Lundholm, 1955 — NW Namibia. granti Thomas & Schwann, 1904 — Northern Cape Province (South Africa). MDDnop hawker: Thomas, 1901 — W Sudan, Eritrea. isabellinus Cretzschmar, 1826 — Egypt, Sudan, Eritrea. Ean mediterraneus Wagner, 1841 — Sardinia. schlumberger: Remy Saint-Loup, 1894 — NE Morocco. sinaiticus Hemprich & Ehrenberg, 1832 — Egypt, Iraq. S whitakeri Thomas, 1902 — Libya, Niger and Algeria. The Cape Hare occurs in the Mediterranean I of Sardinia and in isolated populations scattered throughout most of the Arabian Peninsula and the Middle East and E to W Himalayas. This species has an extensive range in Africa which is separated in two distinct regions. First, in Egypt, Sudan, South Sudan, Eritrea, Ethiopia, Uganda, Kenya, and Tanzania, and throughout most of the dry savanna regions of C, W & N Africa, including parts of the Sahara Desert. Second, in savanna and semi-desert regions of Namibia, Botswana, S Zimbabwe, SW Mozambique, South Africa, Swaziland, and Lesotho.
Distribution. Notably disjunct distribution in Madagascar with separate populations in the N (moister forests of the Sambirano region and in scattered forest fragments on the slopes of the Tsaratanana Massif), the NW (two areas, one ranging from the Manongarivo Special Reserve to the Mahavavy du Nord River, and a more S extension from the Betsiboka River and Ankarafantsika National Park N to the Maevarano River), and the CE (NE of Antananarivo, N of the Mangoro River as far as the Ambatovaky Special Reserve); the distribution in the N part of its range and its relation to the White-fronted Brown Lemur (FE. albifrons) remain unclear; generally speaking, it occurs inland of the range of the White-fronted Brown Lemur, but additional surveys are needed. Introduced on the Comoros Is. in Lemuridae
Distribution. Notably disjunct distribution in Madagascar with separate populations in the N (moister forests of the Sambirano region and in scattered forest fragments on the slopes of the Tsaratanana Massif), the NW (two areas, one ranging from the Manongarivo Special Reserve to the Mahavavy du Nord River, and a more S extension from the Betsiboka River and Ankarafantsika National Park N to the Maevarano River), and the CE (NE of Antananarivo, N of the Mangoro River as far as the Ambatovaky Special Reserve); the distribution in the N part of its range and its relation to the White-fronted Brown Lemur (FE. albifrons) remain unclear; generally speaking, it occurs inland of the range of the White-fronted Brown Lemur, but additional surveys are needed. Introduced on the Comoros Is.
Distribution. Albertine Rift region of NE DR Congo, Uganda, W Rwanda, and NW Burundi, from Lake Albert to the headwaters of the Kagera River, and the Itombwe Massif in the S; there is a narrow eastern distributional extension to just W of the Nile, where it occurs in forest patches such as Mabira and Mpanga, and a record from Moroto in N Uganda. in Galagidae
Distribution. Albertine Rift region of NE DR Congo, Uganda, W Rwanda, and NW Burundi, from Lake Albert to the headwaters of the Kagera River, and the Itombwe Massif in the S; there is a narrow eastern distributional extension to just W of the Nile, where it occurs in forest patches such as Mabira and Mpanga, and a record from Moroto in N Uganda.
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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.