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Distribution. SE Guinea, E Liberia, S Ivory Coast, and W Ghana; populations ofeither this species, the Ivory Coast White-toothed Shrew (C. eburnea), or both species are found in S Sierra Leone and are included in the range map ofthis species but have not been investigated genetically and could represent either species. There are apparently records that represent this species from S Nigeria, although further research is needed to confirm thatthis speciesis truly found there. in Soricidae
Distribution. SE Guinea, E Liberia, S Ivory Coast, and W Ghana; populations ofeither this species, the Ivory Coast White-toothed Shrew (C. eburnea), or both species are found in S Sierra Leone and are included in the range map ofthis species but have not been investigated genetically and could represent either species. There are apparently records that represent this species from S Nigeria, although further research is needed to confirm thatthis speciesis truly found there.
Distribution. Widely distributed in South-east Asia (Myanmar, Laos, Thailand, Cambodia, S Vietnam, and Peninsular Malaysia, including offshore islands). Distribution boundary between this species and the Large White-toothed Shrew (C. dracula), especially in Myanmar or whether their distributions overlapped, is not clear. in Soricidae
Distribution. Widely distributed in South-east Asia (Myanmar, Laos, Thailand, Cambodia, S Vietnam, and Peninsular Malaysia, including offshore islands). Distribution boundary between this species and the Large White-toothed Shrew (C. dracula), especially in Myanmar or whether their distributions overlapped, is not clear.
Distribution. Islands off peninsular Thailand (Koh Samui) and Peninsular Malaysia (Tioman, and Mapur); one old specimen from Mt Tahan, Pahang State, Malaysia, might also belong to this species, but no recent confirmation of this taxon on the Malay Peninsula cast doubts about the existence of such a continental population of Peninsular White-toothed Shrew. in Soricidae
Distribution. Islands off peninsular Thailand (Koh Samui) and Peninsular Malaysia (Tioman, and Mapur); one old specimen from Mt Tahan, Pahang State, Malaysia, might also belong to this species, but no recent confirmation of this taxon on the Malay Peninsula cast doubts about the existence of such a continental population of Peninsular White-toothed Shrew.
FIGURE 4 in Reinstatement of "Hippolyte St. Pauli" Brandt, 1851 as a valid species of Lebbeus White, 1847 (Decapoda: Caridea: Thoridae)
FIGURE 4. Lebbeus sanctipauli (Brand, 1851), male (cl 7.0 mm; TUF). A, carapace and left cephalic appendages, lateral view; B, rostrum and anterior part of carapace, lateral view; C, endopod of left pleopod 1, dorsal (anterior) view; D, appendices interna and masculina of left pleopod 2, dorsomesial view.
FIGURE 3 in Reinstatement of "Hippolyte St. Pauli" Brandt, 1851 as a valid species of Lebbeus White, 1847 (Decapoda: Caridea: Thoridae)
FIGURE 3. Lebbeus sanctipauli (Brand, 1851), female (cl 8.7 mm; CBM-ZC 10176), left thoracic appendages. A, maxilliped 3, lateral view; B, same appendage, distal part of ultimate article, extensor view; C, same appendage, distal part of antepenultimate article, lateral view; D, pereopod 1, lateral view; E, same appendage, chela, extensor view; F, same appendage, tip of fingers; G, pereopod 2, lateral view; H, pereopod 3, lateral view; I, same appendage, dactylus and distal part of propodus, lateral view; J, pereopod 4, lateral view; K, pereopod 5, lateral view.
FIGURE 5 in Reinstatement of "Hippolyte St. Pauli" Brandt, 1851 as a valid species of Lebbeus White, 1847 (Decapoda: Caridea: Thoridae)
FIGURE 5. Lebbeus polaris (Sabine, 1824). A–E, female (cl 11.0 mm; HUMZ-C 1368); F, G, male (cl 10.7 mm; same lot). A, carapace and left cephalic appendages, lateral view; B, rostrum and anterior part of carapace, lateral view; C, telson, dorsal view; D, right pereopod 3, lateral view; E, same appendage, dactylus and distal part of propodus, lateral view; F, carapace and cephalic right appendages, lateral view; G, rostrum and anterior part of carapace, lateral view.
FIGURE 2 in Reinstatement of "Hippolyte St. Pauli" Brandt, 1851 as a valid species of Lebbeus White, 1847 (Decapoda: Caridea: Thoridae)
FIGURE 2. Lebbeus sanctipauli (Brand, 1851), female (cl 8.7 mm; CBM-ZC 10176). A, rostrum, lateral view; B, anterior part of carapace and cephalic appendages, dorsal view (marginal setae on antennal scaphocerites omitted); C, telson, dorsal view; D, same, posterior margin, dorsal view.
FIGURE 1 in Reinstatement of "Hippolyte St. Pauli" Brandt, 1851 as a valid species of Lebbeus White, 1847 (Decapoda: Caridea: Thoridae)
FIGURE 1. Lebbeus sanctipauli (Brand, 1851), female (cl 8.7 mm; CBM-ZC 10176), habitus in lateral view.
Distribution. WC core and SE peninsula of Sulawesi, including Mt Kanino, Mt Nokilalaki, Mt Lehio, Rano Rano, and Mamasa regions, Quarles Range, Mt Rantemario, and Mt Latimojong. Descriptive notes. er 155-242 mm, tail 138-190 mm, ear 23-29 mm, hind-foot 28-45 mm; weight 95-170 g. The Montane Hill Rat is the largest member of the B. fratrorum species group, with broad head, long rostrum, and robust body. Pelage is moderately long, soft, and lustrous, with shortish blackish guard hairs mixed throughout. Dorsum is brownish gray, speckled with buff that is a mix of dark gray underfur and overhairs with brown tips and buffy bands, being dark gray for the most part. Sides are paler grayish brown and fade into ventral pelage. Sides of muzzle are white. Venter is grayish white or dark grayish white, although some are grayish buff, with gray hairs and unpigmented tips or unpigmented altogether, respectively. Juveniles are duller and darker, with more grayish white underparts. Feet are long and slender, with white digits. Ears are large, covered in short unpigmented hair, rubbery, and gray and brown hues. Tail is 88-102% of head-body length and mainly bicolored, brownish gray to blackish gray dorsally and glossy white ventrally, with white tip most of the time. Scrotum is gray. Skull is large, with long and wide rostrum and narrow zygomatic plate. Fleas (e.g. Sigmactenus, Stivalius, Musserella, and Dasypsyllus), ticks (Rhipicephalus) pseudoscorpions (Magachernes and Chiridiochernes), and nematodes (Bunomystrongylus and Sibulura) have been recorded from the Montane Hill Rat. There are two pairs of inguinal mammae. Chromosomal complement is 2n = 42, FN = 60 (females) or FN = 61 (males). in Muridae
Distribution. WC core and SE peninsula of Sulawesi, including Mt Kanino, Mt Nokilalaki, Mt Lehio, Rano Rano, and Mamasa regions, Quarles Range, Mt Rantemario, and Mt Latimojong. Descriptive notes. er 155-242 mm, tail 138-190 mm, ear 23-29 mm, hind-foot 28-45 mm; weight 95-170 g. The Montane Hill Rat is the largest member of the B. fratrorum species group, with broad head, long rostrum, and robust body. Pelage is moderately long, soft, and lustrous, with shortish blackish guard hairs mixed throughout. Dorsum is brownish gray, speckled with buff that is a mix of dark gray underfur and overhairs with brown tips and buffy bands, being dark gray for the most part. Sides are paler grayish brown and fade into ventral pelage. Sides of muzzle are white. Venter is grayish white or dark grayish white, although some are grayish buff, with gray hairs and unpigmented tips or unpigmented altogether, respectively. Juveniles are duller and darker, with more grayish white underparts. Feet are long and slender, with white digits. Ears are large, covered in short unpigmented hair, rubbery, and gray and brown hues. Tail is 88-102% of head-body length and mainly bicolored, brownish gray to blackish gray dorsally and glossy white ventrally, with white tip most of the time. Scrotum is gray. Skull is large, with long and wide rostrum and narrow zygomatic plate. Fleas (e.g. Sigmactenus, Stivalius, Musserella, and Dasypsyllus), ticks (Rhipicephalus) pseudoscorpions (Magachernes and Chiridiochernes), and nematodes (Bunomystrongylus and Sibulura) have been recorded from the Montane Hill Rat. There are two pairs of inguinal mammae. Chromosomal complement is 2n = 42, FN = 60 (females) or FN = 61 (males).
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003). in Muridae
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003).
Although previously treated as a subspecies of G. dolichurus, G.dryas was later recognized as a good species. Monotypic. Distribution. Restricted to elevations above 1000 m within the Albertine Rift Mts. Descriptive notes. Head-body 100-130 mm, tail 142-177 mm, car 15-21 mm, hindfoot 22-28 mm; weight 30-59 g. Fur of the Albertine Rift Thicket Rat is tawny brown above, becoming brighter orange brown on rump, with sharply demarcated pure white belly bordered by thin orange line. Tail is very long (160% of head-body length), semi-prehensile, tufted, and dark brown. Feet are pale buff, with four digits on forefoot and five on relatively short hindfoot, fifth digit longer and semi-opposable. Females have 0+2 = 2 pairs of nipples. in Muridae
Although previously treated as a subspecies of G. dolichurus, G.dryas was later recognized as a good species. Monotypic. Distribution. Restricted to elevations above 1000 m within the Albertine Rift Mts. Descriptive notes. Head-body 100-130 mm, tail 142-177 mm, car 15-21 mm, hindfoot 22-28 mm; weight 30-59 g. Fur of the Albertine Rift Thicket Rat is tawny brown above, becoming brighter orange brown on rump, with sharply demarcated pure white belly bordered by thin orange line. Tail is very long (160% of head-body length), semi-prehensile, tufted, and dark brown. Feet are pale buff, with four digits on forefoot and five on relatively short hindfoot, fifth digit longer and semi-opposable. Females have 0+2 = 2 pairs of nipples.
FIGURE. The colour of the florets in solitary or corymbose synflorescences of Callilepis species. A. Solitary capitulum of the shrubby C. caerulea with white ray and disc florets collected at Blouberg by Kremer-Köhne (Photographer M. Koekemoer). B. Solitary capitulum of the perennial herb C. leptophylla with white ray and purplish disc florets growing at Nylsvlei (Photographer M. Koekemoer). C. Solitary capitulum of the perennial herb C. leptophylla with white ray and disc florets growing in Pretoria (Photographer S.P. Bester). D. Corymbose synflorescence of the perennial herb C. normae with white ray and disc florets from the type locality (Photographer M. Koekemoer). in A taxonomic revision of the genus Callilepis (Asteraceae) in South Africa
FIGURE. The colour of the florets in solitary or corymbose synflorescences of Callilepis species. A. Solitary capitulum of the shrubby C. caerulea with white ray and disc florets collected at Blouberg by Kremer-Köhne (Photographer M. Koekemoer). B. Solitary capitulum of the perennial herb C. leptophylla with white ray and purplish disc florets growing at Nylsvlei (Photographer M. Koekemoer). C. Solitary capitulum of the perennial herb C. leptophylla with white ray and disc florets growing in Pretoria (Photographer S.P. Bester). D. Corymbose synflorescence of the perennial herb C. normae with white ray and disc florets from the type locality (Photographer M. Koekemoer).
FIGURES 13–15 in Kiwisaldula waiho and K. hurunui, two new species of Saldidae (Hemiptera: Heteroptera) from the South Island of New Zealand, with redescriptions of K. butleri (White) and K. laelaps (White)
FIGURES 13–15. Eunomy (left corium), most frequently observed pigmentation patterns. (13) Kiwisaldula waiho, (14) K. butleri, (15) K. laelaps.
FIGURES 9–12 in Kiwisaldula waiho and K. hurunui, two new species of Saldidae (Hemiptera: Heteroptera) from the South Island of New Zealand, with redescriptions of K. butleri (White) and K. laelaps (White)
FIGURES 9–12. Facial views of Kiwisaldula species; males. (9) K. waiho, (10) K. hurunui, (11) K. butleri, (12) K. laelaps.
FIGURES 5–8 in Kiwisaldula waiho and K. hurunui, two new species of Saldidae (Hemiptera: Heteroptera) from the South Island of New Zealand, with redescriptions of K. butleri (White) and K. laelaps (White)
FIGURES 5–8. Dorsal views of type specimens with labels. Scale bar = 1 mm. (5–6) Kiwisaldula butleri, female holotype and labels, (7–8) K. laelaps, male lectotype and labels.
FIGURES 1–4 in Kiwisaldula waiho and K. hurunui, two new species of Saldidae (Hemiptera: Heteroptera) from the South Island of New Zealand, with redescriptions of K. butleri (White) and K. laelaps (White)
FIGURES 1–4. Dorsal views of Kiwisaldula species (males; legs and antennae omitted). Scale bar = 1 mm. (1) K. waiho, (2) K. hurunui, (3) K. butleri, (4) K. laelaps.
FIGURES 16–23 in Kiwisaldula waiho and K. hurunui, two new species of Saldidae (Hemiptera: Heteroptera) from the South Island of New Zealand, with redescriptions of K. butleri (White) and K. laelaps (White)
FIGURES 16–23. Schematic view of male genitalia (16–19) Paramere, ventral view. (16) Kiwisaldula waiho (shaft base broken), (17) K. hurunui (shaft base broken), (18a–b) K. butleri, (19) K. laelaps. (20–23) Parandria, posterior view. (20) K. waiho, (21) K. hurunui, (22) K. butleri, (23) K. laelaps.
FIGURE 2. Bairdia fasciata Brady, the holotype. A. The white slide 1.16.44 in "What's in a name?" Bairdia fasciata Brady, 1870, and two new Caribbean species of Bairdoppilata (Bairdiidae, Podocopida, Ostracoda)
FIGURE 2. Bairdia fasciata Brady, the holotype. A. The white slide 1.16.44 is labelled in Kenneth G. McKenzie's handwriting: "Bairdia fasciata Brady, 1869 (Fonds). B97. HOLOTYPE. Loc: St. Vincent, Cape de Verde Islands. KGM 1967 (in pencil)". It contains a single carapace, which is illustrated in Fig. C. B. The red slide 2.05.44 is labelled in G. S. Brady's handwriting: Bairdia fasciata B., Cythere curvirostrata B., St Vincent, Cape de Verd. There are no specimens on this slide. C. Low-resolution snapshot of the carapace in the white slide. "The holotype is cloudy white, but with a little adjustment of lighting it shows a saddle-shaped opaque area. The image is tilted to compensate for the tilt of the mounted specimen, but there may still be a slight distortion of the actual outline (it may look a little more elongate than it actually is)" (observations by DJH 1 September 2022).
FIGURE 10 in Meatopida gen. nov., a new genus to accommodate two species originally described in Atopida White, 1846 (Coleoptera: Scirtoidea: Scirtidae)
FIGURE 10. Meatopida dorsale (Broun), female genitalia. A) genital tract, B) coxites and styli, C) prehensor. Scale bar (A) = 0.5 mm.
FIGURE 9 in Meatopida gen. nov., a new genus to accommodate two species originally described in Atopida White, 1846 (Coleoptera: Scirtoidea: Scirtidae)
FIGURE 9. Meatopida dorsale (Broun), male genitalia in dorsal (A, C, E) and dorsolateral (B, D, F) view. A, B), specimen from Waitaanga Plateau, C, D), specimen from Erua, E, F), specimen from Great Barrier Island.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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