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.
378
datasets available to search
ShareScore release 0.9.0
Dataset results
378 results for “widespread species”
FIGURE 4 in A new species of Cis Latreille (Coleoptera: Ciidae) widespread in Brazil but with similarities to the African fauna
FIGURE 4. Dissected fourth instar larva of Cis caramelo sp. nov. from Cariacica, in the state of Espírito. Head (a), showing maxillae (mx), mandibles (md), frontal arms (f.a.), and antennae (black arrows). Part of the ventro-lateral view of thorax (b), focusing on the first left leg. Abdomen (c) in lateral view, showing the segments VI-VIII and the spiracles (red arrows). Posterior portion of abdomen (d) in ventral view, showing the urogomphi (ug). Scale bars: 0.1 mm.
FIGURE 3 in A new species of Cis Latreille (Coleoptera: Ciidae) widespread in Brazil but with similarities to the African fauna
FIGURE 3. Eggs, larva and pupa of Cis caramelo sp. nov. from Cariacica, in the state of Espírito Santo. Three eggs (a, red arrows) in the pores of Trametes versicolor. Fourth instar larva in lateral view (b) and detail of the abdominal apex (c). Pupa (d). Scale bars: 0.5 mm.
FIGURE 2 in A new species of Cis Latreille (Coleoptera: Ciidae) widespread in Brazil but with similarities to the African fauna
FIGURE 2. Cis caramelo sp. nov., females. Dorsal view of a paratype from Cariacica, in the state of Espírito Santo (a). Abdominal terminalia of a paratype from the same locality (b–c), showing the ovipositor (b) and the VIII sternite with the spiculum ventrale (c). Scale bars: 0.5 mm (a), 0.1 mm (b–c).
FIGURE 1 in A new species of Cis Latreille (Coleoptera: Ciidae) widespread in Brazil but with similarities to the African fauna
FIGURE 1. Cis caramelo sp. nov., males. Holotype from Cariacica, in the state of Espírito Santo, in dorsal (a), lateral (b) and ventral view (c). Small paratype from the same locality in dorsal view (d). The first two abdominal ventrites of specimens from Cariacica and showing a large circular (e) and a small oval (f) setose sex patch. Abdominal terminalia in a specimen from Cariacica, showing the VIII sternite (g), basal piece (h), tegmen (i) and penis (j). Scale bars: 0.5 mm (a–d), 0.2 mm (e–f), 0.1 mm (g–j).
Data from: Morphometrics and redescription of Aphyllon fasciculatum and Aphyllon franciscanum (Orobanchaceae), two widespread but previously conflated species in western North America
<p>We continue the taxonomic reevaluation of <em>Aphyllon</em> sect. <em>Aphyllon</em> by describing a widespread species throughout Western North America previously recognized within a polyphyletic <em>A. fasciculatum</em>. To support our description and revised key, we analyzed fifteen continuous and discrete characters across 156 herbarium specimens and iNaturalist observations sampled from across the geographic range. Principal component and multiple correspondence analyses reveal clear variation in floral characters. Discriminant analyses show that floral color, the calyx cup to calyx lobe ratio, calyx lobe length, and degree of bend in the corolla tube are useful distinguishing features, but not diagnostic in every case.</p>
Distribution. Widespread in the C and W regions of S Africa, reaching to about 15° N in SW Angola. Occupies mainly arid and semi-arid areas, but also occurs in regions with higher precipitation and denser vegetation, such as the fynbos biome of South Africa's Western Cape Province. Cape Foxes have expanded their range over recent decades to the SW, where the species reaches the Atlantic and Indian Ocean coastlines. May occur in SW Swaziland, and possibly also in Lesotho. in Canidae
Distribution. Widespread in the C and W regions of S Africa, reaching to about 15° N in SW Angola. Occupies mainly arid and semi-arid areas, but also occurs in regions with higher precipitation and denser vegetation, such as the fynbos biome of South Africa's Western Cape Province. Cape Foxes have expanded their range over recent decades to the SW, where the species reaches the Atlantic and Indian Ocean coastlines. May occur in SW Swaziland, and possibly also in Lesotho.
Figs 19 & 20 in Detailed iconography of the widespread Neotropical millipede, Myrmecodesmus hastatus (Schubart, 1945), and the first record of the species from the Caribbean area (Diplopoda, Polydesmida, Pyrgodesmidae)
Figs 19 & 20. Right gonopod of a male of Myrmecodesmus hastatus (Schubart, 1945), from Saint-Pierre, Martinique, subventral and subdorsal views, respectively. Scale bar: 0.2 mm. Del. S. Golovatch. Designations: fl – flagellum; sl – solenomere.
Fig. 18 in Detailed iconography of the widespread Neotropical millipede, Myrmecodesmus hastatus (Schubart, 1945), and the first record of the species from the Caribbean area (Diplopoda, Polydesmida, Pyrgodesmidae)
Fig. 18. Habitus of a male of Myrmecodesmus hastatus (Schubart, 1945), from Saint-Pierre, Martinique, lateral view. Picture by D. VandenSpiegel.
Distribution. Widespread in the C and W regions of S Africa, reaching to about 15° N in SW Angola. Occupies mainly arid and semi-arid areas, but also occurs in regions with higher precipitation and denser vegetation, such as the fynbos biome of South Africa's Western Cape Province. Cape Foxes have expanded their range over recent decades to the SW, where the species reaches the Atlantic and Indian Ocean coastlines. May occur in SW Swaziland, and possibly also in Lesotho. in Canidae
Distribution. Widespread in the C and W regions of S Africa, reaching to about 15° N in SW Angola. Occupies mainly arid and semi-arid areas, but also occurs in regions with higher precipitation and denser vegetation, such as the fynbos biome of South Africa's Western Cape Province. Cape Foxes have expanded their range over recent decades to the SW, where the species reaches the Atlantic and Indian Ocean coastlines. May occur in SW Swaziland, and possibly also in Lesotho.
Distribution. Mostly in E New Guinea with one record in West Papua Province and one record each from Salawati and New Ireland Is; possibly on New Britain and SudestIs; there was a recent acoustic record from Manus I that probably is a member of this species complex, but this needs confirmation with a specimen, and the species is most likely widespread in W New Guinea. in Vespertilionidae
Distribution. Mostly in E New Guinea with one record in West Papua Province and one record each from Salawati and New Ireland Is; possibly on New Britain and SudestIs; there was a recent acoustic record from Manus I that probably is a member of this species complex, but this needs confirmation with a specimen, and the species is most likely widespread in W New Guinea.
Distribution. Presumably found across New Guinea (possibly widespread in N lowlands) and also on Raja Ampat Is (Waigeo and Salawati); distributional limits between this species and the Steadfast Tube-nosed Fruit Bat (FP. tenax) are uncertain, and thus distribution given here is tentative. in Pteropodidae
Distribution. Presumably found across New Guinea (possibly widespread in N lowlands) and also on Raja Ampat Is (Waigeo and Salawati); distributional limits between this species and the Steadfast Tube-nosed Fruit Bat (FP. tenax) are uncertain, and thus distribution given here is tentative.
Subspecies and Distribution. A.l.lerviaPallas,1777—Morocco,NA.l.,andNTunisia. A.l.angusiRothschild,1921—NWNiger(Air&TermitMassifs). A.l.blaineiRothschild,1913—SELybia,NEChad,andNW&NESudan(probablynowrestrictedtoRedSeahills). A.l.fassiniLepri,1930—NWLibya,extremeSTunisia. A.l.ornatus1.GeoffroySaint-Hilaire,1827—SE&SWEgypt. A. l. sahariensis Rothschild, 1913 — S Morocco, Western Sahara, NW Mauritania, S A.l ria, extreme S Libya, NE Mali, SE Niger, and NW Chad. Introduced, free-ranging populations occur in S Spain, the Canary Is, USA (California, New Mexico, and Texas), and NE Mexico. Subspecies of free-ranging introduced populations are unknown because they originate from zoo animals of uncertain origin or from hybrids. Most introduced populations are probably from subspecies lervia, derived from European zoos. The Aoudad has become a widespread invasive species. in Bovidae
Subspecies and Distribution. A.l.lerviaPallas,1777—Morocco,NA.l.,andNTunisia. A.l.angusiRothschild,1921—NWNiger(Air&TermitMassifs). A.l.blaineiRothschild,1913—SELybia,NEChad,andNW&NESudan(probablynowrestrictedtoRedSeahills). A.l.fassiniLepri,1930—NWLibya,extremeSTunisia. A.l.ornatus1.GeoffroySaint-Hilaire,1827—SE&SWEgypt. A. l. sahariensis Rothschild, 1913 — S Morocco, Western Sahara, NW Mauritania, S A.l ria, extreme S Libya, NE Mali, SE Niger, and NW Chad. Introduced, free-ranging populations occur in S Spain, the Canary Is, USA (California, New Mexico, and Texas), and NE Mexico. Subspecies of free-ranging introduced populations are unknown because they originate from zoo animals of uncertain origin or from hybrids. Most introduced populations are probably from subspecies lervia, derived from European zoos. The Aoudad has become a widespread invasive species.
Distribution. Restricted to the cooler waters of the N Atlantic Ocean from 71° 30" N in the Norwegian Sea, Iceland, and [Labrador (Canada) in the N, to Madeira, Azores, and NE USA to the S; single records from the Gulf of Mexico and E Mediterranean Sea are thought to represent vagrant individuals. In general, this species appears to be more widespread in E Atlantic Ocean than in W Atlantic Ocean, which may be related to preferences for cooler water temperatures. in Ziphiidae
Distribution. Restricted to the cooler waters of the N Atlantic Ocean from 71° 30" N in the Norwegian Sea, Iceland, and [Labrador (Canada) in the N, to Madeira, Azores, and NE USA to the S; single records from the Gulf of Mexico and E Mediterranean Sea are thought to represent vagrant individuals. In general, this species appears to be more widespread in E Atlantic Ocean than in W Atlantic Ocean, which may be related to preferences for cooler water temperatures.
Distribution. New Guinea, widespread but patchily distributed except from SW lowlands, also on Yapen I. It has been reported in the Bird's Head (= Vogelkop) Peninsula, but it is uncertain if the species definitely occurs there. in Dasyuridae
Distribution. New Guinea, widespread but patchily distributed except from SW lowlands, also on Yapen I. It has been reported in the Bird's Head (= Vogelkop) Peninsula, but it is uncertain if the species definitely occurs there.
Distribution. Known from only two isolated localities (Ingwavuma and Ubombo) on E slopes of Lebombo Mts, KwaZulu-Natal Province, E South Africa; owl pellet remains from Weenen, ¢.250 km SW of type locality, appear to represent this species, suggesting that it is more widespread than currently recognized. Possibly extends into SE Swaziland along the Lebombo Mts. in Chrysochloridae
Distribution. Known from only two isolated localities (Ingwavuma and Ubombo) on E slopes of Lebombo Mts, KwaZulu-Natal Province, E South Africa; owl pellet remains from Weenen, ¢.250 km SW of type locality, appear to represent this species, suggesting that it is more widespread than currently recognized. Possibly extends into SE Swaziland along the Lebombo Mts.
Figs 1–17 in Detailed iconography of the widespread Neotropical millipede, Myrmecodesmus hastatus (Schubart, 1945), and the first record of the species from the Caribbean area (Diplopoda, Polydesmida, Pyrgodesmidae)
Figs 1–17. SEM micrographs of a male of Myrmecodesmus hastatus (SCHUBART, 1945), from Saint-Pierre, Martinique: habitus, lateral view (1); anterior part of body, lateral and dorsal views, respectively (2 & 5); midbody segments, lateral view (3); caudal part of body, lateral, dorsal and ventral views, respectively (4, 6 & 7); metatergal microsculpture, caudal view (8); cross-section of a midbody segment, caudal view (9); midbody paratergite, lateral view (10); tergal microsculpture with limbus, dorsal view (11); midbody sternite, ventral view (12); midbody leg, lateral view (13); left gonopod, submesal, subventral, subcaudal and mesal views, respectively (14–17). Scale bars: 0.5 mm (1), 0.1 mm (2–7 & 9), 0.05 mm (10 & 13–13), 0.02 mm (8, 11 & 12).
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).
nad1 alignment in Description of three widespread new Peronospora species parasitising Caryophyllales
Open the record for dataset details and reuse information.
COX2/cox2-1 spacer/COX1 alignment in Description of three widespread new Peronospora species parasitising Caryophyllales
Open the record for dataset details and reuse information.
ITS alignment in Description of three widespread new Peronospora species parasitising Caryophyllales
Open the record for dataset details and reuse information.
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.