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Subspecies and Distribution. S. J. fuscicollis Spix, 1823 — W Brazil (states of Acre & Amazonas) and Peru, S of the Rio Solimoes, between the Rio Javari in the W, E through the Rio Jutai Basin to the Rio Jurua (left bank), also in Peru, W of the Rio Yavari as far as the Rio Tapiche, an E tributary of the Rio Ucayali, and extending N from there as far as the Rio Blanco (left bank), where it meets the distribution of Geoffroy's Saddle-back Tamarin, S. nigrifrons (right bank of the Rio Blanco). S. f. auvilapiresi Hershkovitz, 1966 — W Brazil in the Amazonas State (type locality is the mouth of the Lago de Tefé, Rio Solimoes), found along the S of the Rio Solimoes between the rios Jurua and Purus, including the basins of the rios Urucu and Coari, and probably the Rio Tefé; the S limits are not known but possibly in the region of the N bank of the Rio Tapaua, an affluent of the Rio Purus. S. f. eruzlimai Hershkovitz, 1966 — W Brazil, described by Hershkovitz without provenance (based on a single individual "said to be from the upper Rio Purus"); M. G. M. van Roosmalen reported in 2003 that it had been observed by T. van Roosmalen on 21 June 2002, on the W bank of the Rio Purus, opposite the mouth of the Rio Sepatini, and noted that Hershkovitz was correct in supposing that it occurred between the rios Pauini and Tapaua, W of the Rio Purus. S. J. mura Rohe et al, 2009 — C Brazil (Amazonas State), interfluvium of the rios Madeira and Purus, S of the Rio Amazonas, probably S to the Rio Igapo-Acu. S. f. primitivus Hershkovitz, 1977 — W Brazil (Amazonas State), the distribution is believed to extend from the left bank of the Rio Pauini, along the left bank of the upper Rio Purus, N to the Rio Tapaua (right bank), as far W the right bank of the Rio Jurua, and the Rio Tarauaca. in Callitrichiade
Subspecies and Distribution. S. J. fuscicollis Spix, 1823 — W Brazil (states of Acre & Amazonas) and Peru, S of the Rio Solimoes, between the Rio Javari in the W, E through the Rio Jutai Basin to the Rio Jurua (left bank), also in Peru, W of the Rio Yavari as far as the Rio Tapiche, an E tributary of the Rio Ucayali, and extending N from there as far as the Rio Blanco (left bank), where it meets the distribution of Geoffroy's Saddle-back Tamarin, S. nigrifrons (right bank of the Rio Blanco). S. f. auvilapiresi Hershkovitz, 1966 — W Brazil in the Amazonas State (type locality is the mouth of the Lago de Tefé, Rio Solimoes), found along the S of the Rio Solimoes between the rios Jurua and Purus, including the basins of the rios Urucu and Coari, and probably the Rio Tefé; the S limits are not known but possibly in the region of the N bank of the Rio Tapaua, an affluent of the Rio Purus. S. f. eruzlimai Hershkovitz, 1966 — W Brazil, described by Hershkovitz without provenance (based on a single individual "said to be from the upper Rio Purus"); M. G. M. van Roosmalen reported in 2003 that it had been observed by T. van Roosmalen on 21 June 2002, on the W bank of the Rio Purus, opposite the mouth of the Rio Sepatini, and noted that Hershkovitz was correct in supposing that it occurred between the rios Pauini and Tapaua, W of the Rio Purus. S. J. mura Rohe et al, 2009 — C Brazil (Amazonas State), interfluvium of the rios Madeira and Purus, S of the Rio Amazonas, probably S to the Rio Igapo-Acu. S. f. primitivus Hershkovitz, 1977 — W Brazil (Amazonas State), the distribution is believed to extend from the left bank of the Rio Pauini, along the left bank of the upper Rio Purus, N to the Rio Tapaua (right bank), as far W the right bank of the Rio Jurua, and the Rio Tarauaca.
Data from: Loss of fungal symbionts at the arid limit of the distribution range in a native Patagonian grass – resource ecophysiological relations
<p>1. Crucial to our understanding of plant ecology is the consideration of the eco-physiological responses and constraints of plant-fungal symbioses throughout the native distribution range of their host.</p> <p>2. We examined key eco-physiological roles of two co-occurring fungal symbionts [Epichloë endophytes and arbuscular mycorrhizal fungi (AMF)] in the endemic grass Hordeum comosum across a wide bioclimatic gradient and contrasting grazing severity. We sampled H. comosum plants along four humid-to-arid transects in Patagonia, Argentina, covering its entire distribution range and determined Epichloë presence, AMF root colonization, nitrogen and phosphorus concentration, intrinsic water use-efficiency (iWUE, the ratio of photosynthesis to stomatal conductance) and 18O-enrichment of cellulose in shoots.</p> <p>3. Root colonization by AMF increased with Epichloë-presence. All plants hosted Epichloë in the humid range of the gradient, but symbioses occurrence decreased towards arid sites which also displayed severe grazing symptoms at site level.</p> <p>4. Symbiosis with Epichloë correlated positively with shoot nitrogen concentration in the centre of the distribution range, and with shoot phosphorus concentration across the entire distribution range.</p> <p>5. The site-level relationship of AMF colonization with 18O-enrichment and iWUE suggested that mycorrhiza boosted stomatal conductance in humid environments but curbed it in arid environments.</p> <p>6. While the interpretation of interactions and potential causalities from observational studies should be done with caution, this study demonstrates distinct correlations between plant-fungal symbiont associations and key resource parameters (phosphorus, nitrogen, and iWUE vs 18O-enrichment). Such correlations may suggest particular functional roles for these symbionts in the ecology of their host plant.</p>
Distribution. SE California, Arizona, S Colorado, New Mexico, and perhaps S Utah and W Texas; distributional limits in NC Mexico are uncertain, considering it has been recorded only in several localities in Chihuahua and a disjunct site near Texcoco, in the Distrito Federal. in Vespertilionidae
Distribution. SE California, Arizona, S Colorado, New Mexico, and perhaps S Utah and W Texas; distributional limits in NC Mexico are uncertain, considering it has been recorded only in several localities in Chihuahua and a disjunct site near Texcoco, in the Distrito Federal.
Subspecies and Distribution. M. f. fortidens G. S. Miller & G. M. Allen, 1928 — Mexico, from N Sinaloa S along narrow strip on Pacific coast and from Veracruz S to Chiapas, and Guatemala. M. f. sonoriensis Findley & C. Jones, 1967 — at least Sonora and N Sinaloa in NW Mexico. Distributional limits of subspecies are obscure. in Vespertilionidae
Subspecies and Distribution. M. f. fortidens G. S. Miller & G. M. Allen, 1928 — Mexico, from N Sinaloa S along narrow strip on Pacific coast and from Veracruz S to Chiapas, and Guatemala. M. f. sonoriensis Findley & C. Jones, 1967 — at least Sonora and N Sinaloa in NW Mexico. Distributional limits of subspecies are obscure.
Distribution. SE Alaska S to Canada along Pacific coast and extending along lower one-third of Canada; widely distributed in the USA, with exception of SW & SE coasts, with S limit in NE Mexico (Sierra de San Carlos). in Vespertilionidae
Distribution. SE Alaska S to Canada along Pacific coast and extending along lower one-third of Canada; widely distributed in the USA, with exception of SW & SE coasts, with S limit in NE Mexico (Sierra de San Carlos).
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.
Distribution. Mexico (from S Sonora on Pacific slope and C Tamaulipas on Gulf coast to S and including Yucatan Peninsula) and Central America to N Costa Rica (S limit is Cordillera de Talamanca). in Phyllostomidae
Distribution. Mexico (from S Sonora on Pacific slope and C Tamaulipas on Gulf coast to S and including Yucatan Peninsula) and Central America to N Costa Rica (S limit is Cordillera de Talamanca).
Subspecies and Distribution. P. m. maxwelli C.H. Smith, 1827 — Senegal and Gambia to E Ghana (likely limited to the E by the Volta River). P.m. danei Hinton, 1920 — Yatward and Sherbro Is, Sierra Leone. in Bovidae
Subspecies and Distribution. P. m. maxwelli C.H. Smith, 1827 — Senegal and Gambia to E Ghana (likely limited to the E by the Volta River). P.m. danei Hinton, 1920 — Yatward and Sherbro Is, Sierra Leone.
Distribution. WC Iran (SW & NW ofthe city of Isfahan), but its distribution limits are undetermined, especially to the E. in Bovidae
Distribution. WC Iran (SW & NW ofthe city of Isfahan), but its distribution limits are undetermined, especially to the E.
Distribution. Discontinuous and limited to wetland environments in the Congo Basin N and W of the range of the Zambezi Sitatunga in S Benin (Porto Novo), S Nigeria, Cameroon, Central African Republic, Equatorial Guinea, Gabon, Republic of the Congo, N DR Congo; also several isolated populations in W Africa (Senegal, Gambia & Guinea-Bissau), NE Nigeria and W Chad, and perhaps extreme S Ghana. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments in the Congo Basin N and W of the range of the Zambezi Sitatunga in S Benin (Porto Novo), S Nigeria, Cameroon, Central African Republic, Equatorial Guinea, Gabon, Republic of the Congo, N DR Congo; also several isolated populations in W Africa (Senegal, Gambia & Guinea-Bissau), NE Nigeria and W Chad, and perhaps extreme S Ghana. Maps and distributional information here are provisional pending future research.
Distribution. Discontinuous and limited to wetland environments in SE Sudan, perhaps the Rift Valley of Ethiopia, W Kenya surrounding Lake Victoria (two locations, very rare), Uganda, Burundi, Rwanda, NW Tanzania, and NE DR Congo. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments in SE Sudan, perhaps the Rift Valley of Ethiopia, W Kenya surrounding Lake Victoria (two locations, very rare), Uganda, Burundi, Rwanda, NW Tanzania, and NE DR Congo. Maps and distributional information here are provisional pending future research.
Distribution. Lowlands of EC Ethiopia (Awash area) and NW Somalia. The exact southern limit of the Northern Lesser Kudu''s distribution in eastern Ethiopia requires additional research. in Bovidae
Distribution. Lowlands of EC Ethiopia (Awash area) and NW Somalia. The exact southern limit of the Northern Lesser Kudu''s distribution in eastern Ethiopia requires additional research.
Distribution. Discontinuous and limited to wetland environments in two areas of S Sudan: small swamps in SW Sudan near the DR Congo border, where the type specimen was collected, and the Sudd Swamps (Bahr-el-Ghazal) of the upper White Nile. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments in two areas of S Sudan: small swamps in SW Sudan near the DR Congo border, where the type specimen was collected, and the Sudd Swamps (Bahr-el-Ghazal) of the upper White Nile. Maps and distributional information here are provisional pending future research.
Subspecies and Distribution. T.o.oryxPallas,1766—SAfricaincludingNamibia,Botswana,Swaziland,andSouthAfrica. T. o. livingstonii Sclater, 1864 — S & E Africa; N limit through Angola and S DR Congo, then N to Rwanda, Uganda, SE Sudan, SW Ethiopia, Kenya, S Somalia, and Tanzania. in Bovidae
Subspecies and Distribution. T.o.oryxPallas,1766—SAfricaincludingNamibia,Botswana,Swaziland,andSouthAfrica. T. o. livingstonii Sclater, 1864 — S & E Africa; N limit through Angola and S DR Congo, then N to Rwanda, Uganda, SE Sudan, SW Ethiopia, Kenya, S Somalia, and Tanzania.
Distribution. Discontinuous and limited to wetland environments from S Republic of the Congo through C DR Congo and SW Tanzania, S to Zambia, Angola, and Botswana. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments from S Republic of the Congo through C DR Congo and SW Tanzania, S to Zambia, Angola, and Botswana. Maps and distributional information here are provisional pending future research.
Distribution. Limits of distribution are unresolved but currently known to occur on Mt Damavand and in Central Alborz (= Elburz) Mts of Teheran and Mazandaran provinces, N Iran. in Calomyscidae
Distribution. Limits of distribution are unresolved but currently known to occur on Mt Damavand and in Central Alborz (= Elburz) Mts of Teheran and Mazandaran provinces, N Iran.
Distribution. Limits of distribution unknown but includes the Great Balkhan Mts of W Turkmenistan and the W & C Kopet Dag of S Turkmenistan and NE Iran. in Calomyscidae
Distribution. Limits of distribution unknown but includes the Great Balkhan Mts of W Turkmenistan and the W & C Kopet Dag of S Turkmenistan and NE Iran.
Distribution. Limits of distribution unresolved but currently known from W & S Iran (Zagros Mts as far E as the Kerman Province and the N Genu Mts of Hormozgan Province); it may occur in S & SE Turkey (Gaziantep and Hakkari provinces). in Calomyscidae
Distribution. Limits of distribution unresolved but currently known from W & S Iran (Zagros Mts as far E as the Kerman Province and the N Genu Mts of Hormozgan Province); it may occur in S & SE Turkey (Gaziantep and Hakkari provinces).
Distribution. SE Australia, from the McPherson and Border ranges in SE Queensland, S to Victoria and SE South Australia; it is absent from the coastal drainages of the Great Dividing Range, S at least to the Wallamba River, and W of the Great Dividing Range in New South Wales (but it probably occurs to the limit of tree growth on the Southern Tableland), and from the inland draining catchments of the Murray Basin in Victoria. in Acrobatidae
Distribution. SE Australia, from the McPherson and Border ranges in SE Queensland, S to Victoria and SE South Australia; it is absent from the coastal drainages of the Great Dividing Range, S at least to the Wallamba River, and W of the Great Dividing Range in New South Wales (but it probably occurs to the limit of tree growth on the Southern Tableland), and from the inland draining catchments of the Murray Basin in Victoria.
Distribution. SW Asia, Kopet Dag Mts and Malyy Balkhan Mts of SW Turkmenistan and NE Iran; historic remains from WC Afghanistan discussed under taxonomy. Distributional limits are not known. in Gliridae
Distribution. SW Asia, Kopet Dag Mts and Malyy Balkhan Mts of SW Turkmenistan and NE Iran; historic remains from WC Afghanistan discussed under taxonomy. Distributional limits are not known.
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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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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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