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325 results for “Distribution limits”
Distribution. Brazilian Amazon, S from the Rio Iriri at least as far as the S (left) margin of the Rio Peixoto de Azevedo (E tributary of the Rio Teles Pires), the S limits are not beyond the headwaters and upper Rio Paraguay (c.14° 30' S), the upper Rio Teles Pires evidently marks the W limit. in Callitrichiade
Distribution. Brazilian Amazon, S from the Rio Iriri at least as far as the S (left) margin of the Rio Peixoto de Azevedo (E tributary of the Rio Teles Pires), the S limits are not beyond the headwaters and upper Rio Paraguay (c.14° 30' S), the upper Rio Teles Pires evidently marks the W limit.
Subspecies and Distribution. P.b.bilabiatumWagner,1843—E&SBrazil,Paraguay,andNEArgentina(Misiones). P.b. magnum Owen & Webster, 1983 — SE Bolivia (Santa Cruz Department) and NW Argentina (Salta Province). Records from Suriname (including the type of S. microdon by W. K. H. Peters in 1863) are controversial; several authors consider that this was probably a mistake in the annotated locality. Despite intense collecting efforts in Suriname in the last 40 years, there was no record of Pygoderma; its northern limit is E Brazil, and it is only known from Cerrado and Mata Atlantica ecoregions. No voucheris securely assigned to a Suriname location, so it is not included as part ofits distribution. in Phyllostomidae
Subspecies and Distribution. P.b.bilabiatumWagner,1843—E&SBrazil,Paraguay,andNEArgentina(Misiones). P.b. magnum Owen & Webster, 1983 — SE Bolivia (Santa Cruz Department) and NW Argentina (Salta Province). Records from Suriname (including the type of S. microdon by W. K. H. Peters in 1863) are controversial; several authors consider that this was probably a mistake in the annotated locality. Despite intense collecting efforts in Suriname in the last 40 years, there was no record of Pygoderma; its northern limit is E Brazil, and it is only known from Cerrado and Mata Atlantica ecoregions. No voucheris securely assigned to a Suriname location, so it is not included as part ofits distribution.
Distribution. Disjunct range in Ghana, Togo, Benin, SE Nigeria, Cameroon, extreme S South Sudan, NE DR Congo, SE Uganda, and W Kenya; limits uncertain. in Nesomyidae
Distribution. Disjunct range in Ghana, Togo, Benin, SE Nigeria, Cameroon, extreme S South Sudan, NE DR Congo, SE Uganda, and W Kenya; limits uncertain.
Distribution. Limited to the Amazon River Basin and most ofits tributaries in Colombia, Ecuador, and Peru. It may also extend into the Orinoco River system in Venezuela, but itis uncertain if sightings there were this species or the Guiana Dolphin (S. guianensus). in Delphinidae
Distribution. Limited to the Amazon River Basin and most ofits tributaries in Colombia, Ecuador, and Peru. It may also extend into the Orinoco River system in Venezuela, but itis uncertain if sightings there were this species or the Guiana Dolphin (S. guianensus).
Distribution. SW Colombia (Putumayo Department), in the Colombian Amazon between the upper rios Caqueta and Putumayo, which form the N and S limits ofits distribution, respectively, with the foothills of the Andes to the W; the E limit ofits distribution is poorly known, but it likely intergrades with that of the Yellow-handed Titi (C. lucifer), which occurs further E in the Caqueta-Putumayo interfluvium. in Phitheciidae
Distribution. SW Colombia (Putumayo Department), in the Colombian Amazon between the upper rios Caqueta and Putumayo, which form the N and S limits ofits distribution, respectively, with the foothills of the Andes to the W; the E limit ofits distribution is poorly known, but it likely intergrades with that of the Yellow-handed Titi (C. lucifer), which occurs further E in the Caqueta-Putumayo interfluvium.
Distribution. Brazilian Amazon, S of the right (S) bank of the Solimoes-Madeira river system and N of the Canuma, Uraria, and Ramos channels ("paranas"), which form the N limit of the distribution of Hoffmanns's Titi (C. hoffmannsi). in Phitheciidae
Distribution. Brazilian Amazon, S of the right (S) bank of the Solimoes-Madeira river system and N of the Canuma, Uraria, and Ramos channels ("paranas"), which form the N limit of the distribution of Hoffmanns's Titi (C. hoffmannsi).
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.
Distribution. Brazilian Amazon Basin, in the Solimoes-Tapajos interfluvium, S of the Canuma, Uraria, and Ramos channels ("paranas"), which form the S limit of the distribution of the Lake Baptista Titi (C. baptista); the distribution is limited to the W by the Rio Abacaxis. in Phitheciidae
Distribution. Brazilian Amazon Basin, in the Solimoes-Tapajos interfluvium, S of the Canuma, Uraria, and Ramos channels ("paranas"), which form the S limit of the distribution of the Lake Baptista Titi (C. baptista); the distribution is limited to the W by the Rio Abacaxis.
Distribution. SE coastal Madagascar, known from the Manombo Special Reserve, S of the Manampatrana River and N of the Mananara River. The precise N and S limits of the range are unknown. in Lepilemuridae
Distribution. SE coastal Madagascar, known from the Manombo Special Reserve, S of the Manampatrana River and N of the Mananara River. The precise N and S limits of the range are unknown.
Distribution. NW Madagascar, restricted to the region of Ambato-Boéni and Ankarafantsika, where the remaining forests are highly fragmented, with the N limit appearing to be near Analalava on the Bay of Narinda, and it is also found S and W of the Betsiboka River at Katsepy and on the shores of Lac Kinkony, on both sides of the Mahavavy River, and in the Tsiombikibo Classified Forest near Mitsinjo. Introduced to the Comoros Is. in Lemuridae
Distribution. NW Madagascar, restricted to the region of Ambato-Boéni and Ankarafantsika, where the remaining forests are highly fragmented, with the N limit appearing to be near Analalava on the Bay of Narinda, and it is also found S and W of the Betsiboka River at Katsepy and on the shores of Lac Kinkony, on both sides of the Mahavavy River, and in the Tsiombikibo Classified Forest near Mitsinjo. Introduced to the Comoros Is.
Distribution. NW Madagascar from near Bealalana in the N to the Betsiboka River, S limit is reportedly Ambato Boeni, and E boundary is near Antetemasy (just W of Befandriana Nord). in Indriidae
Distribution. NW Madagascar from near Bealalana in the N to the Betsiboka River, S limit is reportedly Ambato Boeni, and E boundary is near Antetemasy (just W of Befandriana Nord).
Distribution. Restricted range in NE Madagascar, limited to an extremely small area in the Ampandraha, Madirabe, and Daraina districts bounded by the Loky River in the N and the Manambato River in the S; its distribution is centered on the town of Daraina and covers ¢.245,000 ha. in Indriidae
Distribution. Restricted range in NE Madagascar, limited to an extremely small area in the Ampandraha, Madirabe, and Daraina districts bounded by the Loky River in the N and the Manambato River in the S; its distribution is centered on the town of Daraina and covers ¢.245,000 ha.
Distribution. Salta and Catamarca provinces (N & W of Sierra de Ambato and Sierra de Manchao), NW Argentina, but limits still unresolved. in Cricetidae
Distribution. Salta and Catamarca provinces (N & W of Sierra de Ambato and Sierra de Manchao), NW Argentina, but limits still unresolved.
Subspecies and Distribution. H.l.larLinnaeus,1771—MalayPeninsula,from9°NtotheMudahRiverandSofthePerakRiver. H.l.carpenteriGroves,1968—EMyanmar,NWLaos,andNWThailand,fromChiengDaoat19°22°Nto¢.16°N.H..entelloides1.GeoffroySaint-Hilaire,1842—SMyanmarandSWThailand,fromc.15°No10°N. H.l.vestitusG.S.Miller,1942—NSumatra,NWofLakeTobaandtheSingkilRiver. H. l. yunnanensis Ma & Wang, 1986 — S China (SW Yunnan Province), the northernmost subspecies, originally between the Nujiang (= Salween) and Lancangjiang (= Mekong) rivers in the counties of Cangyuan, Menglian, and Ximeng; by the 1960s limited to the Nangun River at elevations of 1000-1500 m, but now probably extinct there. in Hylobatidae
Subspecies and Distribution. H.l.larLinnaeus,1771—MalayPeninsula,from9°NtotheMudahRiverandSofthePerakRiver. H.l.carpenteriGroves,1968—EMyanmar,NWLaos,andNWThailand,fromChiengDaoat19°22°Nto¢.16°N.H..entelloides1.GeoffroySaint-Hilaire,1842—SMyanmarandSWThailand,fromc.15°No10°N. H.l.vestitusG.S.Miller,1942—NSumatra,NWofLakeTobaandtheSingkilRiver. H. l. yunnanensis Ma & Wang, 1986 — S China (SW Yunnan Province), the northernmost subspecies, originally between the Nujiang (= Salween) and Lancangjiang (= Mekong) rivers in the counties of Cangyuan, Menglian, and Ximeng; by the 1960s limited to the Nangun River at elevations of 1000-1500 m, but now probably extinct there.
Distribution. NC DRCongo, a few localities in the Congo Basin on left bank of the Congo River; its exact distribution is unknown but is probably related to the forest block extension and limited by rivers. in Muridae
Distribution. NC DRCongo, a few localities in the Congo Basin on left bank of the Congo River; its exact distribution is unknown but is probably related to the forest block extension and limited by rivers.
Figure 5 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)
Figure 5. The principal component analysis result of the eight studied sand fly species according to the January mean temperature limits of the species.
FIGURE 21 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 21. Emertonia hessleri sp. nov. Female (holotype): A, P5 (missing outer basal seta indicated by arrow); B, P6 and genital field. Male (allotype): C, P5 (missing outer basal seta indicated by arrow); D, P6. Scale bar = 0.01 mm.
FIGURE 20 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 20. Emertonia hessleri sp. nov. Female. A, P1 (paratype 4); B, P2 (holotype); C, P3 with intercoxal sclerite (holotype); D, P4 (holotype). Scale bar = 0.03 mm.
FIGURE 4 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 4. Emertonia serrata sp. nov. Female (paratype 1). A, antennule, overview (armature omitted); B, disarticulated antennulary segments showing armature. Scale bar = 0.02 mm.
FIGURE 8 in Deep sea without limits-four new closely related species of Emertonia Wilson 1932 (Copepoda: Harpacticoida: Paramesochridae) show characters with a worldwide distribution
FIGURE 8. Emertonia serrata sp. nov. Male (allotype). A, habitus, dorsal view; B, habitus, lateral view; C, caudal ramus, ventral view. Scale bars = a, b, 0.05 mm; c, 0.02 mm.
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