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Distribution. SE Kenya and NE Tanzania. The Fringe-eared Oryx is geographically separated from the Galla Oryx by the Tana River and Aberdare Mts in S Kenya. Its range began to spread into the Serengeti in the 1970s. in Bovidae
Distribution. SE Kenya and NE Tanzania. The Fringe-eared Oryx is geographically separated from the Galla Oryx by the Tana River and Aberdare Mts in S Kenya. Its range began to spread into the Serengeti in the 1970s.
Distribution. It ranges through temperate zone forests and paramos from the Cordillera Central in C Colombia through the Cordillera Oriental of Ecuador to the eastern Andean cloud forests in Peru, southward to Junin department. The exact range is unknown and there are obvious distributional gaps. One major natural gap is the dry forest south of the Huancabamba depression, which separates the northern population from the main Peruvian population. in Cervidae
Distribution. It ranges through temperate zone forests and paramos from the Cordillera Central in C Colombia through the Cordillera Oriental of Ecuador to the eastern Andean cloud forests in Peru, southward to Junin department. The exact range is unknown and there are obvious distributional gaps. One major natural gap is the dry forest south of the Huancabamba depression, which separates the northern population from the main Peruvian population.
Distribution. Two geographically disjunct ranges, including arid parts of extreme SW Angola, W Namibia, and W South Africa S to Western Cape Province, and N Mozambique, E & S Zimbabwe, extreme E Botswana, and N South Africa; an 800km-gap separates the two parts of the species' range between Augrabies Falls on the Orange River in W South Africa and the Magaliesberg of North West and Gauteng provinces in N South Africa. in Molossidae
Distribution. Two geographically disjunct ranges, including arid parts of extreme SW Angola, W Namibia, and W South Africa S to Western Cape Province, and N Mozambique, E & S Zimbabwe, extreme E Botswana, and N South Africa; an 800km-gap separates the two parts of the species' range between Augrabies Falls on the Orange River in W South Africa and the Magaliesberg of North West and Gauteng provinces in N South Africa.
Distribution. Widely distributed in tropical forest belt of Africa extending from Senegal in W to E DR Congo in the FE; there is a separate population restricted to coastal Kenya, Tanzania (including Pemba and Unguja Is in Zanzibar Archipelago), and NE Mozambique, with scattered records from Zambia, S Malawi, N Zimbabwe, and WC Mozambique. in Nycteridae
Distribution. Widely distributed in tropical forest belt of Africa extending from Senegal in W to E DR Congo in the FE; there is a separate population restricted to coastal Kenya, Tanzania (including Pemba and Unguja Is in Zanzibar Archipelago), and NE Mozambique, with scattered records from Zambia, S Malawi, N Zimbabwe, and WC Mozambique.
Distribution. Broadly distributed in at least two widely separated populations: one in E Africa (E Uganda, extreme SW Ethiopia, W & S Kenya, and N & W Tanzania), the other in S Africa (S Angola, NE Namibia, N Botswana, W Zambia, and extreme W Zimbabwe); isolated population in Jebel Marra, W Sudan. in Nesomyidae
Distribution. Broadly distributed in at least two widely separated populations: one in E Africa (E Uganda, extreme SW Ethiopia, W & S Kenya, and N & W Tanzania), the other in S Africa (S Angola, NE Namibia, N Botswana, W Zambia, and extreme W Zimbabwe); isolated population in Jebel Marra, W Sudan.
Data for: Separation of oil vapor by polyether block amide composite membrane modified with porous materials
<p>The ability of membranes to separate oil vapor is affected by their permeance and selectivity. This study modifies polyether block amide (PEBA) composite membranes with a microporous zeolite, Silicalite-1, or a mesoporous zeolite, MCM-41. The results show that when PEBA composite membranes are modified with these zeolites, the selective layer of the composite membrane is coated more thinly, resulting in a higher flux of organic gas. Silicalite-1 increases the hydrophobicity of the membrane, which facilitates the adsorption of organic vapor on the membrane surface, thus improving the membrane selectivity. In the separation of oil vapor, both modified membranes can effectively increase the gas permeabilities and selectivities. The main mechanism governing gas transport in the MCM-41-modified membrane is Knudsen diffusion, so the selectivity for small molecules is improved more significantly. By contrast, the dissolution–diffusion mechanism is dominant in the Silicalite-1-modified membranes, which considerably increases the selectivity for large molecules.</p>
Phase separation of competing memories along the human hippocampal theta rhythm.
<p>Data set for Phase separation of competing memories along the human hippocampal theta rhythm.</p>
Distribution. Endemic to N Pacific Ocean, the majority ofrecords come from W North America from 32° 42° N to 54° 18' N, also recorded on the Pacific coast ofJapan from 35% to 41° 42° N. This suggests that distribution of this species spans the N Pacific Ocean, but with no records from the C Pacific Ocean, it remains possible that there are separate E and W populations. It has been suggested that distribution of this species is related to the deep current system of the subarctic. in Ziphiidae
Distribution. Endemic to N Pacific Ocean, the majority ofrecords come from W North America from 32° 42° N to 54° 18' N, also recorded on the Pacific coast ofJapan from 35% to 41° 42° N. This suggests that distribution of this species spans the N Pacific Ocean, but with no records from the C Pacific Ocean, it remains possible that there are separate E and W populations. It has been suggested that distribution of this species is related to the deep current system of the subarctic.
Distribution. Endemic to Australia, in two di ¶ unct regions separated by Great Sandy Desert: W region is smallcst and comprises the W part of Pilbara region of Westem Australia, and E region largest and includes NE Western Australia (Kimberley region), N Northern Territory, and NW Queensland. in Rhinonycteridae
Distribution. Endemic to Australia, in two di ¶ unct regions separated by Great Sandy Desert: W region is smallcst and comprises the W part of Pilbara region of Westem Australia, and E region largest and includes NE Western Australia (Kimberley region), N Northern Territory, and NW Queensland.
Subspecies and Distribution. P.n.nasutaE.GeoffroySaint-Hilaire,1804—EAustraliafrommid-NQueenslandStoVictoria. P.n. pallescens Thomas, 1923 — far N Queensland, with geographically separate populations in Wet Tropics and on Cape York Peninsula. in Peramelidae
Subspecies and Distribution. P.n.nasutaE.GeoffroySaint-Hilaire,1804—EAustraliafrommid-NQueenslandStoVictoria. P.n. pallescens Thomas, 1923 — far N Queensland, with geographically separate populations in Wet Tropics and on Cape York Peninsula.
Subspecies and Distribution. L. ¢c. capensis Linnaeus, 1758 — Western Cape Province (South Africa). L.c.aegyptiusDesmarest,1822—Egypt,Sudan,Palestine. L.c.aquiloThomas&Wroughton,1907—SMozambique. L. c. arabicus Hemprich & Ehrenberg, 1832 — Middle East, Arabian Peninsula, Iran, SW Pakistan (Baluchistan), and SW Afghanistan. . ¢. atlanticus de Winton, 1898 — Morocco. ¢. carpi Lundholm, 1955 — NW Namibia. granti Thomas & Schwann, 1904 — Northern Cape Province (South Africa). MDDnop hawker: Thomas, 1901 — W Sudan, Eritrea. isabellinus Cretzschmar, 1826 — Egypt, Sudan, Eritrea. Ean mediterraneus Wagner, 1841 — Sardinia. schlumberger: Remy Saint-Loup, 1894 — NE Morocco. sinaiticus Hemprich & Ehrenberg, 1832 — Egypt, Iraq. S whitakeri Thomas, 1902 — Libya, Niger and Algeria. The Cape Hare occurs in the Mediterranean I of Sardinia and in isolated populations scattered throughout most of the Arabian Peninsula and the Middle East and E to W Himalayas. This species has an extensive range in Africa which is separated in two distinct regions. First, in Egypt, Sudan, South Sudan, Eritrea, Ethiopia, Uganda, Kenya, and Tanzania, and throughout most of the dry savanna regions of C, W & N Africa, including parts of the Sahara Desert. Second, in savanna and semi-desert regions of Namibia, Botswana, S Zimbabwe, SW Mozambique, South Africa, Swaziland, and Lesotho. in Leporidae
Subspecies and Distribution. L. ¢c. capensis Linnaeus, 1758 — Western Cape Province (South Africa). L.c.aegyptiusDesmarest,1822—Egypt,Sudan,Palestine. L.c.aquiloThomas&Wroughton,1907—SMozambique. L. c. arabicus Hemprich & Ehrenberg, 1832 — Middle East, Arabian Peninsula, Iran, SW Pakistan (Baluchistan), and SW Afghanistan. . ¢. atlanticus de Winton, 1898 — Morocco. ¢. carpi Lundholm, 1955 — NW Namibia. granti Thomas & Schwann, 1904 — Northern Cape Province (South Africa). MDDnop hawker: Thomas, 1901 — W Sudan, Eritrea. isabellinus Cretzschmar, 1826 — Egypt, Sudan, Eritrea. Ean mediterraneus Wagner, 1841 — Sardinia. schlumberger: Remy Saint-Loup, 1894 — NE Morocco. sinaiticus Hemprich & Ehrenberg, 1832 — Egypt, Iraq. S whitakeri Thomas, 1902 — Libya, Niger and Algeria. The Cape Hare occurs in the Mediterranean I of Sardinia and in isolated populations scattered throughout most of the Arabian Peninsula and the Middle East and E to W Himalayas. This species has an extensive range in Africa which is separated in two distinct regions. First, in Egypt, Sudan, South Sudan, Eritrea, Ethiopia, Uganda, Kenya, and Tanzania, and throughout most of the dry savanna regions of C, W & N Africa, including parts of the Sahara Desert. Second, in savanna and semi-desert regions of Namibia, Botswana, S Zimbabwe, SW Mozambique, South Africa, Swaziland, and Lesotho.
Distribution. NE South Africa, known only from three small, widely separated locations: Bronberg Ridge area in SE Pretoria, Gauteng Province (18 sites), Nylsvley Nature Reserve and surrounding farms on Nyl floodplain in Modimolle district, Limpopo Province (9 sites), and near Pretoriuskop Camp, Fayi area (Macili and Machulwane), and Numbi Gate in SW Kruger National Park, Mpumalanga Province (4 sites). in Chrysochloridae
Distribution. NE South Africa, known only from three small, widely separated locations: Bronberg Ridge area in SE Pretoria, Gauteng Province (18 sites), Nylsvley Nature Reserve and surrounding farms on Nyl floodplain in Modimolle district, Limpopo Province (9 sites), and near Pretoriuskop Camp, Fayi area (Macili and Machulwane), and Numbi Gate in SW Kruger National Park, Mpumalanga Province (4 sites).
Subspecies and Distribution. C.v.vellerosusGray,1865—Bolivia,NEChile,Paraguay,andhighlandsofNWArgentina;itprobablyalsooccursinSEPeru. C. v. pannosus Thomas, 1902 — lower areas of NC Argentina S to Mendoza, La Pampa, and SW Buenos Aires provinces; a disjunct population also occurs in E Buenos Aires Province, which is separated from the main distribution area by ¢.500 km. in Chlamyphoridae
Subspecies and Distribution. C.v.vellerosusGray,1865—Bolivia,NEChile,Paraguay,andhighlandsofNWArgentina;itprobablyalsooccursinSEPeru. C. v. pannosus Thomas, 1902 — lower areas of NC Argentina S to Mendoza, La Pampa, and SW Buenos Aires provinces; a disjunct population also occurs in E Buenos Aires Province, which is separated from the main distribution area by ¢.500 km.
Subspecies and Distribution. C.o.olivaceusSchomburgk,1848—mightberestrictedtotheVenezuelanAmazonBasinfromtheupperRioOrinoco,andthroughouttheOrinocosavannaabovethemouthoftheRioMeta,asfarNandWastheSierradePerijaandtheVenezuelanC.o.dela C.o. (C.o. Range), to the left bank of the Rio Essequibo in W Guyana, in forests of the Guiana Shield; distributional limits separating the two subspecies are not well known. C. o. castaneus 1. Geoffroy Saint-Hilaire, 1851 — Guianas (possibly from the Rio Essequibo in Guyana E through Suriname and French Guiana) and N Brazil, where its distributional limits are not well known but are possibly marked by the rios Negro and Branco and Catrimani (right bank affluent of the Rio Branco) in the W, the Rio Amazonas in the S, and the Atlantic coast in the E, and it also occurs on Caviana and Mexiana Is in the estuary of the Rio Amazonas. Small numbers introduced as pets are now feral on Margarita I off the Venezuelan coast. in Cebidae
Subspecies and Distribution. C.o.olivaceusSchomburgk,1848—mightberestrictedtotheVenezuelanAmazonBasinfromtheupperRioOrinoco,andthroughouttheOrinocosavannaabovethemouthoftheRioMeta,asfarNandWastheSierradePerijaandtheVenezuelanC.o.dela C.o. (C.o. Range), to the left bank of the Rio Essequibo in W Guyana, in forests of the Guiana Shield; distributional limits separating the two subspecies are not well known. C. o. castaneus 1. Geoffroy Saint-Hilaire, 1851 — Guianas (possibly from the Rio Essequibo in Guyana E through Suriname and French Guiana) and N Brazil, where its distributional limits are not well known but are possibly marked by the rios Negro and Branco and Catrimani (right bank affluent of the Rio Branco) in the W, the Rio Amazonas in the S, and the Atlantic coast in the E, and it also occurs on Caviana and Mexiana Is in the estuary of the Rio Amazonas. Small numbers introduced as pets are now feral on Margarita I off the Venezuelan coast.
Distribution. Brazilian Amazon, S of the Rio Amazonas, between the rios Xingu and Iriri in the states of Para and Mato Grosso. Only three widely separated localities are known, one is relatively close to the type locality and another on the right (S) bank of the Rio Iriri in Para. in Phitheciidae
Distribution. Brazilian Amazon, S of the Rio Amazonas, between the rios Xingu and Iriri in the states of Para and Mato Grosso. Only three widely separated localities are known, one is relatively close to the type locality and another on the right (S) bank of the Rio Iriri in Para.
Distribution. NE Madagascar, confined to the Masoala Peninsula and the region immediately N of the Bay of Antongil, the Antainambalana River appears to separate it from the Black-and-white Ruffed Lemur (V. variegata subcincta), but the W limit of the range remains unclear; it may have occurred as far N as Antalaha in the past, but this Is uncertain. in Lemuridae
Distribution. NE Madagascar, confined to the Masoala Peninsula and the region immediately N of the Bay of Antongil, the Antainambalana River appears to separate it from the Black-and-white Ruffed Lemur (V. variegata subcincta), but the W limit of the range remains unclear; it may have occurred as far N as Antalaha in the past, but this Is uncertain.
Distribution. SW Madagascar (patchily from the Tsiribihina River S to the region of the Onilahy River and the Andringitra Massif) and SE Madagascar from the Mangoro River and the Onive River in the N, with the S limit probably being the Manampatrana River, which, for the most part, separates it from the White-collared Brown Lemur (E. cinereiceps). in Lemuridae
Distribution. SW Madagascar (patchily from the Tsiribihina River S to the region of the Onilahy River and the Andringitra Massif) and SE Madagascar from the Mangoro River and the Onive River in the N, with the S limit probably being the Manampatrana River, which, for the most part, separates it from the White-collared Brown Lemur (E. cinereiceps).
Subspecies and Distribution. H.g.griseusLink,1795—CEMadagascar,roughlyfromtheOnibeRiverStotheOniveRiver(whichmayseparateitfromthesubspeciesgilberti). H.g.gilbert:Rabarivolaetal.,2007—ECMadagascar,knownonlyfromitstypelocalityofBeanamalaoandpresumablyasmallareaNoftheNosivoloRiverandSoftheMangoroandOniverivers. H. g. ranomafanensis Rabarivola et al., 2007 — CW & CE Madagascar, occurs in two, widely separated population pockets, one in the W in the forests of Tsingy de Bemaraha, probably as far as the Betsiboka River, and the other in the E in forests to the S of the Mangoro and Onive rivers (except Beanamalao, the type locality of gilberti). in Lemuridae
Subspecies and Distribution. H.g.griseusLink,1795—CEMadagascar,roughlyfromtheOnibeRiverStotheOniveRiver(whichmayseparateitfromthesubspeciesgilberti). H.g.gilbert:Rabarivolaetal.,2007—ECMadagascar,knownonlyfromitstypelocalityofBeanamalaoandpresumablyasmallareaNoftheNosivoloRiverandSoftheMangoroandOniverivers. H. g. ranomafanensis Rabarivola et al., 2007 — CW & CE Madagascar, occurs in two, widely separated population pockets, one in the W in the forests of Tsingy de Bemaraha, probably as far as the Betsiboka River, and the other in the E in forests to the S of the Mangoro and Onive rivers (except Beanamalao, the type locality of gilberti).
Distribution. Notably disjunct distribution in Madagascar with separate populations in the N (moister forests of the Sambirano region and in scattered forest fragments on the slopes of the Tsaratanana Massif), the NW (two areas, one ranging from the Manongarivo Special Reserve to the Mahavavy du Nord River, and a more S extension from the Betsiboka River and Ankarafantsika National Park N to the Maevarano River), and the CE (NE of Antananarivo, N of the Mangoro River as far as the Ambatovaky Special Reserve); the distribution in the N part of its range and its relation to the White-fronted Brown Lemur (FE. albifrons) remain unclear; generally speaking, it occurs inland of the range of the White-fronted Brown Lemur, but additional surveys are needed. Introduced on the Comoros Is. in Lemuridae
Distribution. Notably disjunct distribution in Madagascar with separate populations in the N (moister forests of the Sambirano region and in scattered forest fragments on the slopes of the Tsaratanana Massif), the NW (two areas, one ranging from the Manongarivo Special Reserve to the Mahavavy du Nord River, and a more S extension from the Betsiboka River and Ankarafantsika National Park N to the Maevarano River), and the CE (NE of Antananarivo, N of the Mangoro River as far as the Ambatovaky Special Reserve); the distribution in the N part of its range and its relation to the White-fronted Brown Lemur (FE. albifrons) remain unclear; generally speaking, it occurs inland of the range of the White-fronted Brown Lemur, but additional surveys are needed. Introduced on the Comoros Is.
Distribution. New Guinea, in the Central Range from Star (= Jayawijaya) Mts in Papua Province, Indonesia, E to between Kratke Range and Wau in Papua New Guinea; also separate populations in the Foja Mts in Papua Province, and N Coastal Ranges and the Huon Peninsula in Papua New Guinea. in Pseudocheiridae
Distribution. New Guinea, in the Central Range from Star (= Jayawijaya) Mts in Papua Province, Indonesia, E to between Kratke Range and Wau in Papua New Guinea; also separate populations in the Foja Mts in Papua Province, and N Coastal Ranges and the Huon Peninsula in Papua New Guinea.
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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.