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525 results for “white species”
Giant sengi or elephant-shrew (Rhynchocyon species) interactions with Red-Capped Robin-Chat (Cossypha natalensis) and White-Chested Alethe (Chamaetylas fuelleborni) in Tanzania
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Data from: Strength and variability of postmating reproductive isolating barriers between four European white oak species
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Data from: Sixteen in one: white-belted Megaselia Rondani (Diptera: Phoridae) from the New World challenge species concepts
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Figure 5 from: Pellegrini MOO, Forzza RC (2017) Synopsis of Commelina L. (Commelinaceae) in the state of Rio de Janeiro, reveals a new white-flowered species endemic to Brazil. PhytoKeys 78: 59-81. https://doi.org/10.3897/phytokeys.78.11932
Figure 5 - Distribution map of Commelina huntii M.Pell.
TABLE 1 in A new species of the thorid shrimp genus Lebbeus White, 1847 (Decapoda: Caridea) from the Amami Rift hydrothermal vent field in the Ryukyu region, Japan
<p><b>TABLE 1.</b> GenBank accession numbers of the mitochondrial COI and 16S rRNA gene sequences from species of <i>Lebbeus</i> used for genetic analyses. *Registered as <i>Lebbeus carinatus</i> de Saint Laurent, 1984 in GenBank.</p><table><tbody><tr><th>Species</th><th>COI</th><th>16S</th></tr></tbody><tbody><tr><th><i>Lebbeus altus</i> Komai, Chang & Chan, 2021</th><td>MZ742156, MZ742157</td><td>-</td></tr><tr><th><i>Lebbeus antarcticus</i> Hale, 1941</th><td>KC494749–KC494752</td><td>-</td></tr><tr><th><i>Lebbeus brevicornis</i> Komai, 2011</th><td>LC831371</td><td>LC831221</td></tr><tr><th><i>Lebbeus compressus</i> (Yokoya, 1933)</th><td>MZ742158, MZ742159</td><td>LC699546</td></tr><tr><th><i>Lebbeus cultrirostris</i> Wang, Sha & Sun, 2023</th><td>OP580068</td><td>OP578210</td></tr><tr><th><i>Lebbeus formosus</i> Komai, Chang & Chan, 2010</th><td>MK409684</td><td>KF023087</td></tr><tr><th><i>Lebbeus fujimotoi</i> Matsuzaki, Hibino & Komai, 2016</th><td>LC699876, LC699877</td><td>LC699547</td></tr><tr><th><i>Lebbeus grandimanus</i> (Bražnikov, 1907)</th><td>MN138399</td><td>-</td></tr><tr><th><i>Lebbeus groenlandicus</i> (Fabricius, 1775)</th><td>DQ882082–DQ882884, FJ581737,</td><td>-</td></tr><tr><th>MG310744, MG312804, MG314359,</th></tr><tr><th>MG314559, MG315672, MG317214,</th></tr><tr><th>MG319295, MG319690, MG319934,</th></tr><tr><th>MG320381, MG320565, MG321028,</th></tr><tr><th></th><td>MG936123, MH242822</td><td></td></tr><tr><th><i>Lebbeus jaolongi</i> (Xu, Liu, Ding & Wang, 2016)</th><td>MH398092</td><td>MH398078</td></tr><tr><th><i>Lebbeus java</i> Komai, Chang & Chan, 2019</th><td>MK409683</td><td>-</td></tr><tr><th><i>Lebbeus kexuei</i> Wang, Sha & Sun, 2023</th><td>OP580069</td><td>OP578211</td></tr><tr><th><i>Lebbeus kiae</i> Schiaparelli, Ahyong & Bowden, 2015</th><td>KT187237–KT187243</td><td>-</td></tr><tr><th><i>Lebbeus laurentae</i> Wicksten, 2010 *</th><td>AF125421</td><td>-</td></tr><tr><th><i>Lebbeus longidactylus</i> (Kobjakova, 1936)</th><td>LC699878</td><td>LC699548</td></tr><tr><th><i>Lebbeus longipes</i> (Kobjakova, 1936)</th><td>LC699879</td><td>LC699549</td></tr><tr><th><i>Lebbeus parvirostris</i> <b>sp. nov.</b></th><td>LC831370</td><td>LC831220</td></tr><tr><th><i>Lebbeus polaris</i> (Sabine, 1824)</th><td>FJ581738, FJ581739, HM425371,</td><td>KP725539, KP772540</td></tr><tr><th>HQ966810, KP759419, KP759420,</th></tr><tr><th>MG310343, MG311624, MG311072,</th></tr><tr><th>MG312952, MG312957, MG313605,</th></tr><tr><th>MG314788, MG315175, MG315873,</th></tr><tr><th>MG316672, MG317268, MG317301,</th></tr><tr><th>MG317705, MG317885, MG318148,</th></tr><tr><th>MG318608, MG318898, MG319773,</th></tr><tr><th>MG319844, MG319853, MG319864,</th></tr><tr><th>MG320139, MG320699, MG321050,</th></tr><tr><th>MG935131, MG935282</th></tr><tr><th><i>Lebbeus rufomaculosus</i> Komai & Matsuzaki, 2022</th><td>LC699872</td><td>LC699542</td></tr><tr><th><i>Lebbeus shinkaiae</i> Komai, Tsuchida & Segonzac,</th><td>MH398097</td><td>MH398083</td></tr><tr><th>2012</th><td></td><td></td></tr><tr><th><i>Lebbeus sokhobio</i> Marin, 2020</th><td>MN590012–MN590015, MN608153–</td><td>-</td></tr><tr><th>MN608155</th></tr><tr><th><i>Lebbeus subtilis</i> Komai & Matsuzaki, 2022</th><td>LC699873</td><td>LC699543</td></tr><tr><th><i>Lebbeus tenuipes</i> Komai & Matsuzaki, 2022</th><td>LC699874, LC699875</td><td>LC699544, LC699545</td></tr><tr><th><i>Lebbeus unalaskensis</i> (Rathbun, 1902)</th><td>-</td><td>LC699550</td></tr><tr><th><i>Lebbeus virentova</i> Nye, Copley, Plouviez & Van</th><td>JQ837265, KJ566966</td><td>KM979548</td></tr><tr><th>Dover, 2012</th></tr></tbody></table>
Figure 13 from: Metzler E, Forbes G (2011) The Lepidoptera of White Sands National Monument, Otero County, New Mexico, USA 4. A new species of Schinia Hübner, 1818 (Lepidoptera, Noctuidae, Heliothinae). ZooKeys 149: 135-144. https://doi.org/10.3897/zookeys.149.1518
Figure 13 - White dune habitat of type locality of Schinia poguei.
Figure 14 from: Metzler E, Forbes G (2011) The Lepidoptera of White Sands National Monument, Otero County, New Mexico, USA 4. A new species of Schinia Hübner, 1818 (Lepidoptera, Noctuidae, Heliothinae). ZooKeys 149: 135-144. https://doi.org/10.3897/zookeys.149.1518
Figure 14 - Distribution map for Schinia poguei.
Figure 3 from: Shiao S, Yang S, Kurahashi H (2014) Keys to the blow flies of Taiwan, with a checklist of recorded species and the description of a new species of Paradichosia Senior-White (Diptera, Calliphoridae). ZooKeys 434: 57-109. https://doi.org/10.3897/zookeys.434.7540
Figure 3 - Pteropleuron (pt) of Bengalia escheri Bezzi, hairs on pteropleuron are largely blackish.
Figure 8 from: Shiao S, Yang S, Kurahashi H (2014) Keys to the blow flies of Taiwan, with a checklist of recorded species and the description of a new species of Paradichosia Senior-White (Diptera, Calliphoridae). ZooKeys 434: 57-109. https://doi.org/10.3897/zookeys.434.7540
Figure 8 - Silbomyia hoeneana Enderlein, ♂. A dorsal view B lateral view.
Figure 7 from: Shiao S, Yang S, Kurahashi H (2014) Keys to the blow flies of Taiwan, with a checklist of recorded species and the description of a new species of Paradichosia Senior-White (Diptera, Calliphoridae). ZooKeys 434: 57-109. https://doi.org/10.3897/zookeys.434.7540
Figure 7 - Paradichosia lui sp. n., ♂. A dorsal view B lateral view.
FIG. 2. Species accumulation curves for all 10 in Bat diversity in the Simandou Mountain Range of Guinea, with the description of a new white-winged vespertilionid
FIG. 2. Species accumulation curves for all 10 sites surveyed at Simandou (2002 RAP and 2008 baseline) generated with EstimateS 8.2.0. Also shown are the Chao1 (dashed line = 42.15) and Chao 2 (dotted line = 45.03), conservative estimates of the total number of species to be expected at Simandou
Figs. 121–127. Prionacalus species. 121 in Revision of the Genus Prionacalus White, 1845 (Coleoptera: Cerambycidae: Prioninae: Prionini)
Figs. 121–127. Prionacalus species. 121) P. simonsi, syntype male, dorsal view; 122) P. simonsi, syntype male, ventral view; 123) P. simonsi, syntype male, labels; 124) P. uniformis, lectotype male, dorsal view; 125) P. uniformis, lectotype male, ventral view; 126–127) P. uniformis, lectotype male same, labels.
Figs. 115–120. Prionacalus species. 115 in Revision of the Genus Prionacalus White, 1845 (Coleoptera: Cerambycidae: Prioninae: Prionini)
Figs. 115–120. Prionacalus species. 115) P. iphis, lectotype male, dorsal view; 116) P. iphis, lectotype, ventral view; 117) P. iphis, lectotype, labels; 118) P. whitei, holotype male, dorsal view; 119) P. whitei, holotype, ventral view; 120) P. whitei, holotype, labels.
FIGURE 6 in A new sympagic nematode species Daptonema gelida sp. n. (Monhysterida, Xyalidae) from the White Sea landfast ice
FIGURE 6. Phylogenetic tree (18S rDNA) derived from Bayesian inference (BI) and Maximum Likelihood (ML) analyses. Branch support provided as ML/BI (SH-aLRT support (%)/posterior probability (%)). The sequence of the new Daptonema species is marked in bold.
FIGURE 2. Lebbeus rufomaculosus n in Three new species of the thorid shrimp genus Lebbeus White, 1847 (Decapoda: Caridea) from Nemuro Strait, Hokkaido, Japan, with supplemental note on L. fujimotoi Matsuzaki, Hibino & Komai, 2015
FIGURE 2. Lebbeus rufomaculosus n. sp., holotype, ovigerous female (cl 16.5 mm), CBM-ZC 16695. A, carapace and left cephalic appendages, lateral view; B, pleon, telson and left pleonal appendages, lateral view.
Distribution. Brazilian Amazon, N of the rios Solimoes and Japura, from the confluence with the Rio Negro in the E, and as far W as the Rio Apaporis, a left (N) bank tributary of the Japura, the N limit is the Negro/Uaupés river system. Its distribution may extend into SE Colombia between the rios Apaporis and Vaupés, where it probably intergrades with the distribution of the White-chested Titi (C. lugens), although there are no data on the ranges of either species from this region. in Phitheciidae
Distribution. Brazilian Amazon, N of the rios Solimoes and Japura, from the confluence with the Rio Negro in the E, and as far W as the Rio Apaporis, a left (N) bank tributary of the Japura, the N limit is the Negro/Uaupés river system. Its distribution may extend into SE Colombia between the rios Apaporis and Vaupés, where it probably intergrades with the distribution of the White-chested Titi (C. lugens), although there are no data on the ranges of either species from this region.
Within Uromys, U. porculus in included in subgenus Cyromys along with the other two Guadalcanal species, namely U. imperator and U. rex. Monotypic. Distribution. Guadalcanal I, Solomon Is. Descriptive notes. Head-body 220 mm, tail 130 mm, ear 19 mm, hindfoot 43 mm. No specific data are available for body weight. The Guadalcanal Giant Rat is the second smallest species in the distinctive genus Uromys. Pelage is short and soft, with longer bristly guard hairs. Dorsal pelage is reddish brown, being browner near head, redder near rump, and grayer as it fades to ventral pelage on the side; ventral pelage is grayish white with grayunderfur. Feet are very broad and of a dull white coloration. Ears are very small and rounded; vibrissae are long. Tail is very short (59% of head-body length), naked, has fine scaling, and is monocolored black. Skull is longer and narrower than that of the King Giant Rat (U. rex), and with narrower molars than in the Emperor Giant Rat (U. imperator). in Muridae
Within Uromys, U. porculus in included in subgenus Cyromys along with the other two Guadalcanal species, namely U. imperator and U. rex. Monotypic. Distribution. Guadalcanal I, Solomon Is. Descriptive notes. Head-body 220 mm, tail 130 mm, ear 19 mm, hindfoot 43 mm. No specific data are available for body weight. The Guadalcanal Giant Rat is the second smallest species in the distinctive genus Uromys. Pelage is short and soft, with longer bristly guard hairs. Dorsal pelage is reddish brown, being browner near head, redder near rump, and grayer as it fades to ventral pelage on the side; ventral pelage is grayish white with grayunderfur. Feet are very broad and of a dull white coloration. Ears are very small and rounded; vibrissae are long. Tail is very short (59% of head-body length), naked, has fine scaling, and is monocolored black. Skull is longer and narrower than that of the King Giant Rat (U. rex), and with narrower molars than in the Emperor Giant Rat (U. imperator).
FIGURES 13–16 in Flesh flies (Diptera: Sarcophagidae) from a white-sand habitat in the Brazilian Amazon, with the description of four new species
FIGURES 13–16. Helicobia cametaensis sp. nov., holotype ♂. 13. Epandrium, surstylus and cercus, left lateral view. 14. Gonites, left lateral view. 15. Distiphallus, ventral view. 16. Distiphallus, left lateral view. Abbreviations: ca = capitis; hp = harpes; jx = juxta, jxl = juxta lateral plate; ls = lateral stylus; prg = pregonite; ptg = postgonite; ve = vesica. Scale bars: 0.1 mm.
FIGURES 27–32 in Flesh flies (Diptera: Sarcophagidae) from a white-sand habitat in the Brazilian Amazon, with the description of four new species
FIGURES 27–32. Lepidodexia (Lepidodexia) grisea Lopes, male from Cametá (MPEG). 27. Wing, dorsal view. 28. Sternite 5, ventral view. 29. Epandrium, surstylus and cercus, left lateral view. 30. Cerci and surstyli, dorsal view. 31. Gonites, left lateral view. 32. Phallus, left lateral view. Abbreviations: bp = basiphallus; jx = juxta; ms = median stylus; prg = pregonite; ptg = postgonite; sl = spinous lobe; ve = vesica. Scale bars: 0.1 mm.
FIGURE 1 in A new species of Angursa (Tardigrada, Heterotardigrada) from the White Sea, North Russia
FIGURE 1. Angursa olenevskii sp. n., heads. A holotype female, dorsal view. B paratype 1, female, ventral view. The continuous punctations of the cuticle is shown just as a band. Scale bars 10 μm.
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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
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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
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