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FIGURE 8. A in On the distribution of the species of the genus Hebius Thompson, 1913 (Squamata Natricidae) in northern Thailand, including the description of a new species and a discussion on snake diversity of this region
FIGURE 8. A. Ventral view of the anterior part of the body of DOR Additional Specimen 7, SHPC11.10.11-14 from Umphang District, Tak Province, showing the 'golden-salmon' pigment accumulations along the edges of the first row of dorsal scales and the corners of the ventral plates, and extending less densely to the edges of the second dorsal row. B. Details of Fig. 11, showing that the pigment accumulations along the edges of the second dorsal row are less dense compared to the first row and ventral corners, and broken up into distinct grains. Photos by Sjon Hauser.
Distribution. Over headwaters of four drainage systems along the E slope of the Andes from Ocobamba, Cusco Region (SE Peru) to Llamachaqui, La Paz Department (W Bolivia). in Caenolestidae
Distribution. Over headwaters of four drainage systems along the E slope of the Andes from Ocobamba, Cusco Region (SE Peru) to Llamachaqui, La Paz Department (W Bolivia).
Subspecies and Distribution. S.t.telumLichtenstein,1823—Kazakhstan(Aktobe,Atyrau,WEastKazakhstan,Karaganda,SKostanay,NKyzylorda,andWestKazakhstanregions). S.t.amankaragaiSelevin,1934—NKazakhstan(NKostanayRegion). S.t.birulaeVinogradov,1937—EKazakhstan(ELakeZaysanBasin)andNWChina(NWXinjiang). S.t.falzferiniBrauner,1913—SUkraine(leftbankoflowerDnieperRiverValleyinMikolaivandKhersonregions). S.t.nastjukoviShenbrot,1991—SKazakhstan(Mangystau,SKyzylorda,Jambyl,andSAlmatyregions),NWUzbekistan(Karakalpakstan),andW&NTurkmenistan(BalkhanandDasoguzregions). S. t. turovi Heptner, 1934 — S European Russia (middle Don Valley in Volgograd and Rostov regions E & S to the right bank of Volga in Astrakhan, Kalmykia, N S.t., and Dagestan). in Dipodidae
Subspecies and Distribution. S.t.telumLichtenstein,1823—Kazakhstan(Aktobe,Atyrau,WEastKazakhstan,Karaganda,SKostanay,NKyzylorda,andWestKazakhstanregions). S.t.amankaragaiSelevin,1934—NKazakhstan(NKostanayRegion). S.t.birulaeVinogradov,1937—EKazakhstan(ELakeZaysanBasin)andNWChina(NWXinjiang). S.t.falzferiniBrauner,1913—SUkraine(leftbankoflowerDnieperRiverValleyinMikolaivandKhersonregions). S.t.nastjukoviShenbrot,1991—SKazakhstan(Mangystau,SKyzylorda,Jambyl,andSAlmatyregions),NWUzbekistan(Karakalpakstan),andW&NTurkmenistan(BalkhanandDasoguzregions). S. t. turovi Heptner, 1934 — S European Russia (middle Don Valley in Volgograd and Rostov regions E & S to the right bank of Volga in Astrakhan, Kalmykia, N S.t., and Dagestan).
Distribution. Maghreb region of North Africa, from SW Western Sahara, Morocco, N Algeria, and Tunisia to W Libya (as far E as Murqub District, and as far S as Fezzan). in Gliridae
Distribution. Maghreb region of North Africa, from SW Western Sahara, Morocco, N Algeria, and Tunisia to W Libya (as far E as Murqub District, and as far S as Fezzan).
Distribution. Australia, in Potter I, the Pilbara region, Carnarvon Basin, and Little Sandy Desert of Western Australia. in Dasyuridae
Distribution. Australia, in Potter I, the Pilbara region, Carnarvon Basin, and Little Sandy Desert of Western Australia.
Subspecies and Distribution. E. k. kalubu Fischer, 1829 — W Papuan Is (Waigeo, Salawati, Misool), and most of New Guinea, including Yapen I and islands NE of mainland (Bagabag, Blup Blup, Kadovar, Karkar, Koil, Vokeo). E. k. cockerelli Ramsay, 1877 — New Britain, Manus, and adjacent islands, in Bismarck Archipelago. E. k. oriomo Tate & Archbold, 1936 — Fly River region, in S New Guinea. E. k. plaulipi Troughton, 1945 — Biak-Supiori and Owi I, in Cenderawasih (= Geelvink) Bay. in Peramelidae
Subspecies and Distribution. E. k. kalubu Fischer, 1829 — W Papuan Is (Waigeo, Salawati, Misool), and most of New Guinea, including Yapen I and islands NE of mainland (Bagabag, Blup Blup, Kadovar, Karkar, Koil, Vokeo). E. k. cockerelli Ramsay, 1877 — New Britain, Manus, and adjacent islands, in Bismarck Archipelago. E. k. oriomo Tate & Archbold, 1936 — Fly River region, in S New Guinea. E. k. plaulipi Troughton, 1945 — Biak-Supiori and Owi I, in Cenderawasih (= Geelvink) Bay.
Subspecies and Distribution. L. t. timidus Linnaeus, 1758 — Scandinavia S to 59° N, N Russia (S to 57° N to 58° N) to E of Ural Mts, Estonia, perhaps Poland, and Altai and Beita Mts in N Xinjiang (China); from Sweden extending in hybrid zones with the subspecies sylvaticus to S coast of Norway and W Latvia. L. t. abet Kuroda, 1938 — Kurile Is (Russia). L. t. ainu Barrett-Hamilton, 1900 — Hokkaido (Japan). L. t. begitschevi Koljuschev, 1936 — Taimyr Peninsula (Russia). L. t. gichiganus J. A. Allen, 1903 — C Yakutia, Kamchatka and Okhotsk Sea coast (Russia). L. t. hibernicus Bell, 1837 — Ireland. L. t. kolymensis Ognev, 1922 — NE Siberia (Russia). L. t. kozhevnikovi Ognev, 1929 — C Russia from 57° to 58°N, whereit intergrades with the nomonotypical timidus S to 53° N. The W boundary is unclear. L. t. lugubris Kastschenko, 1899 — Siberian Altai Mts (Russia). L. t. mordeni Goodwin, 1933 — Russian Far East (Ussuri Valley and lower and middle Amur River) and Heilongjiang (China). L. t. ori Kuroda, 1928 — Sakhalin (Russia). L. t. scoticus Hilzheimer, 1906 — Scotland. L. t. sibiricorumJohansen, 1923 — W & SW Siberia (Russia), N Kazakhstan, and Tacheng Mts in N Xinjiang (China). L. t. sylvaticus Nilsson, 1831 —S Sweden, extending in hybrid zones with nominotypical timidus to S coast of Norway and W Latvia. L. t. transbaikalicus Ognev, 1929 — Trans-Baikal region in E Siberia (Russia) and E Inner Mongolia (= Nei Mongol, China). L. t. varronis Miller, 1901 — at high altitudes in the Alps, C Europe. in Leporidae
Subspecies and Distribution. L. t. timidus Linnaeus, 1758 — Scandinavia S to 59° N, N Russia (S to 57° N to 58° N) to E of Ural Mts, Estonia, perhaps Poland, and Altai and Beita Mts in N Xinjiang (China); from Sweden extending in hybrid zones with the subspecies sylvaticus to S coast of Norway and W Latvia. L. t. abet Kuroda, 1938 — Kurile Is (Russia). L. t. ainu Barrett-Hamilton, 1900 — Hokkaido (Japan). L. t. begitschevi Koljuschev, 1936 — Taimyr Peninsula (Russia). L. t. gichiganus J. A. Allen, 1903 — C Yakutia, Kamchatka and Okhotsk Sea coast (Russia). L. t. hibernicus Bell, 1837 — Ireland. L. t. kolymensis Ognev, 1922 — NE Siberia (Russia). L. t. kozhevnikovi Ognev, 1929 — C Russia from 57° to 58°N, whereit intergrades with the nomonotypical timidus S to 53° N. The W boundary is unclear. L. t. lugubris Kastschenko, 1899 — Siberian Altai Mts (Russia). L. t. mordeni Goodwin, 1933 — Russian Far East (Ussuri Valley and lower and middle Amur River) and Heilongjiang (China). L. t. ori Kuroda, 1928 — Sakhalin (Russia). L. t. scoticus Hilzheimer, 1906 — Scotland. L. t. sibiricorumJohansen, 1923 — W & SW Siberia (Russia), N Kazakhstan, and Tacheng Mts in N Xinjiang (China). L. t. sylvaticus Nilsson, 1831 —S Sweden, extending in hybrid zones with nominotypical timidus to S coast of Norway and W Latvia. L. t. transbaikalicus Ognev, 1929 — Trans-Baikal region in E Siberia (Russia) and E Inner Mongolia (= Nei Mongol, China). L. t. varronis Miller, 1901 — at high altitudes in the Alps, C Europe.
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. 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. Brazil, extreme SE Peru (Pampas del Heath in Madre de Dios Region), Bolivia, Paraguay, and NE Argentina. in Cricetidae
Distribution. Brazil, extreme SE Peru (Pampas del Heath in Madre de Dios Region), Bolivia, Paraguay, and NE Argentina.
Subspecies and Distribution. S. v. imlgans Linnaeus, 1758 — S Scandinavia. S. ıı. alpmus Desmaresl, 1822 - Iberian Peninsula, S France, and Italy. S. v. allaıcıu Screbrennikov, 1928 - Altai of E Russia, N Mongolia, and NW China. S. v. anadyrrmzs Ognev, 1929 - Far N Russia across Siberia. S. u. aıctıcus Trouessart, 1906 - Boreal Siberia lo the Lena River (Russia). S. v. balcanıcus Heinrich, 1936 - E Balkan Peninsula. S. v. chiliensis Sowerby, 1921 — E China. S. v. cinerea Hermann, 1804 — C Europe. S. v. dulkeiti Ognev, 1929 — Amur Region of E Siberia to include Shantar Is (Russia). S. v. exalbidus Pallas, 1779 — W Siberia E of the Ob River (Russia). S. v. fedjushini Ognev, 1935 — Belarus, Lith- uania, Latvia, and Estonia. S. v. formosovi Ognev, 1935 — NW Russia. S. v. fusconigricans Dwigubski, 1804 — Mon- golia and China. S. v. leucourus Kerr, 1792 - Great Britain and Ireland. S. u. lilaeus Miller, 1907 - W Balkan Peninsula. S. v. mantchumw Thomas, 1909 - NE China and Korean Peninsula. S. u. manensr Matschie. 1901 - W Siberia to W of the Ob River, Russia. S. v. ogvmıı Migulin, 1928 - W Russia. S. v. mimtıs Thomas, 1906- Hokkaido 1 (Iapan). S. v. mpalns Thomas, 1907 - Sakhalin (Russia). S. v. ulmımwııs Migulin, 1928 - Ukraine. S. v. vanus Gmelin. 1788 - N Scandinavia. in Sciuridae
Subspecies and Distribution. S. v. imlgans Linnaeus, 1758 — S Scandinavia. S. ıı. alpmus Desmaresl, 1822 - Iberian Peninsula, S France, and Italy. S. v. allaıcıu Screbrennikov, 1928 - Altai of E Russia, N Mongolia, and NW China. S. v. anadyrrmzs Ognev, 1929 - Far N Russia across Siberia. S. u. aıctıcus Trouessart, 1906 - Boreal Siberia lo the Lena River (Russia). S. v. balcanıcus Heinrich, 1936 - E Balkan Peninsula. S. v. chiliensis Sowerby, 1921 — E China. S. v. cinerea Hermann, 1804 — C Europe. S. v. dulkeiti Ognev, 1929 — Amur Region of E Siberia to include Shantar Is (Russia). S. v. exalbidus Pallas, 1779 — W Siberia E of the Ob River (Russia). S. v. fedjushini Ognev, 1935 — Belarus, Lith- uania, Latvia, and Estonia. S. v. formosovi Ognev, 1935 — NW Russia. S. v. fusconigricans Dwigubski, 1804 — Mon- golia and China. S. v. leucourus Kerr, 1792 - Great Britain and Ireland. S. u. lilaeus Miller, 1907 - W Balkan Peninsula. S. v. mantchumw Thomas, 1909 - NE China and Korean Peninsula. S. u. manensr Matschie. 1901 - W Siberia to W of the Ob River, Russia. S. v. ogvmıı Migulin, 1928 - W Russia. S. v. mimtıs Thomas, 1906- Hokkaido 1 (Iapan). S. v. mpalns Thomas, 1907 - Sakhalin (Russia). S. v. ulmımwııs Migulin, 1928 - Ukraine. S. v. vanus Gmelin. 1788 - N Scandinavia.
F in Seed-infesting chalcids of the genus Megastigmus Dalman, 1820 (Hymenoptera: Torymidae) native and introduced to the West Palearctic region: taxonomy, host specificity and distribution
F 6, 7. Compared electroscan dorsal view of thorax of Megastigmus. (6) M. atlanticus X, ex. Cupressus atlantica, Morocco. (7) M. pinsapinis W, ex. Cedrus atlantica, France. Same abbreviations as in (5); axl, axillula; dor, dorsellum; lpm, lateral panel of metanotum; mc, median carina; tsa, transscutal articulation. Scale bar=200 mm.
F in Seed-infesting chalcids of the genus Megastigmus Dalman, 1820 (Hymenoptera: Torymidae) native and introduced to the West Palearctic region: taxonomy, host specificity and distribution
F 130–135. Electroscan photographs of scutellum of female Megastigmus. (130) M. milleri; (131) M. nigrovariegatus; (132) M. pictus; (133) M. pinsapinis; (134) M. pinus; (135) M. pistaciae. Same origins as in (17–22). Scale bars=100 mm.
F in Seed-infesting chalcids of the genus Megastigmus Dalman, 1820 (Hymenoptera: Torymidae) native and introduced to the West Palearctic region: taxonomy, host specificity and distribution
F 11–21. Female antenna of Megastigmus. (11) M. aculeatus, France; (12) M. amicorum, Portugal; (13) M. atedius, France; (14) M. atlanticus, Morocco; (15) M. bipunctatus, France; (16) M. brevicaudis, Poland; (17) M. milleri, the Netherlands; (18) M. nigrovariegatus, France; (19) M. pictus, China; (20) M. pinsapinis, France; (21) M. pinus, Belgium. Scale bar=200 mm.
F in Seed-infesting chalcids of the genus Megastigmus Dalman, 1820 (Hymenoptera: Torymidae) native and introduced to the West Palearctic region: taxonomy, host specificity and distribution
F 40–47. Male antenna of Megastigmus. (40) M. rafni, the Netherlands; (41) M. schimitscheki, Lebanon; (42) M. specularis, Finland; (43) M. spermotrophus, France; (44) M. strobilobius, France; (45) M. suspectus, France; (46) M. transvaalensis Morocco; (47) M. wachtli, Greece. Scale bar=200 mm.
F in Seed-infesting chalcids of the genus Megastigmus Dalman, 1820 (Hymenoptera: Torymidae) native and introduced to the West Palearctic region: taxonomy, host specificity and distribution
F. 10. Male genitalia, M. wachtli X, ex. Cupressus sempervirens, Greece. adg, aedeagus; dgs, digital spine; dig, digitus; par, paramere; phl, phallobase; vls, volsella. Scale bar=100 mm.
FIGURE 2 in Diversity and distribution of the superfamily Grylloidea (Orthoptera: Ensifera: Gryllidea) in the Nearctic region
FIGURE 2. Biogeographical regionalization relationships for the Nearctic region based on Cluster analysis of the superfamily Grylloidea (1° × 1° grid-cells).
FIGURE 13. Croton longicarpus. A. Habit. B. Inflorescence. C. Staminate flower. D. Pistillate flower. E. Capsule. C. lundianus. F. Inflorescence with a noticeable sterile region between the pistillate and staminate flowers. G. Staminate flowers. H in Croton (Euphorbiaceae) of the Brazilian state of Paraná: an annotated checklist, species distribution, and identification key
FIGURE 13. Croton longicarpus. A. Habit. B. Inflorescence. C. Staminate flower. D. Pistillate flower. E. Capsule. C. lundianus. F. Inflorescence with a noticeable sterile region between the pistillate and staminate flowers. G. Staminate flowers. H. Pistillate flowers; note the characteristic white sepals with serrate margins. I. Capsules. C. macrobothrys. J. Trunk, showing red latex where scored with a knife. K. Stipitate acropetiolar nectary glands. L. Young capsule with persistent, bifid stigmas. Photos: A–E: A.P.N. Pereira, F–I: O.L.M. Silva, J–L: R.F. Santos.
FIGURE 6 in Distribution, Regionalization, and Diversity of the dung beetle genus Phanaeus MacLeay (Coleoptera: Scarabaeidae) using Species Distribution Models
FIGURE 6. Beta diversity (β) of Phanaeus within each dominion, segmented by its components (β + β ). total repl rich
Figure 4 in Regional Distribution Of A Brain-Encysting Parasite Provides Insight On Parasite-Induced Host Behavioral Manipulation
Figure 4. Mean (± SE) total brain surface area (A), parasites found per square millimeter of brain surface area (i.e., parasite density) for lowinfection (B) and high-infection (C) treatment groups, and, total parasite numbers found in each brain region for low-infection (D) and high-infection (E) treatment groups, respectively. The brain regions of interest, the telencephalon (black bars), diencephalon/mesencephalon (gray bars), and the rhombencephalon (white bars), are located on the x-axis. In order to make comparisons among individuals, it was necessary to standardize each brain region into sub-regions. That is, both the telencephalon and rhombencephalon were divided into 4 sub-regions of interest. Due to the large surface area covered by the diencephalon/mesencephalon, this area was divided into 10 sub-regions of interest. Note that the figure in (A) illustrates the total brain surface area in each sub-region, which, when compared to the brain surface parasite densities in both treatment groups, shows that the parasite aggregation numbers are not dependent upon available surface area.
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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.