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Distribution. SE Madagascar, in scattered localities between Ranomafana National Park (where it has been seen as far N as Miaranony and Bevoahazo), and as far S as Andringitra National Park and in the forest corridor that connects them, with the distribution possibly extending to the NE as far as the region of Betsakafandrika; there has recently been an unconfirmed sighting of this species to the S in the Vevembe Forest (W of Vondrozo). in Lemuridae
Distribution. SE Madagascar, in scattered localities between Ranomafana National Park (where it has been seen as far N as Miaranony and Bevoahazo), and as far S as Andringitra National Park and in the forest corridor that connects them, with the distribution possibly extending to the NE as far as the region of Betsakafandrika; there has recently been an unconfirmed sighting of this species to the S in the Vevembe Forest (W of Vondrozo).
Subspecies and Distribution. L. f. fasciatus Peron & Lesueur, 1807 — Dorre and Bernier Is, in Shark Bay, Western Australia. Recently introduced into Faure I, also in Shark Bay. in Macropodidae
Subspecies and Distribution. L. f. fasciatus Peron & Lesueur, 1807 — Dorre and Bernier Is, in Shark Bay, Western Australia. Recently introduced into Faure I, also in Shark Bay.
Subspecies and Distribution. R.r.raptorGoldman,1912—EPanama. R. r. hartmanni Enders, 1938 — Pacific slopes of highlands in Costa Rica and W Panama; a recently collected specimen is from a Caribbean lowland locality. in Cricetidae
Subspecies and Distribution. R.r.raptorGoldman,1912—EPanama. R. r. hartmanni Enders, 1938 — Pacific slopes of highlands in Costa Rica and W Panama; a recently collected specimen is from a Caribbean lowland locality.
Distribution. Traditionally known only from the type locality in NW México, but recently found in Cerro de Garnica, NE Michoacan, Mexico. in Cricetidae
Distribution. Traditionally known only from the type locality in NW México, but recently found in Cerro de Garnica, NE Michoacan, Mexico.
Distribution. Known originally from only type locality in S Andean Peru but recently also found in a second locality in Santuario historico de Machu Picchu. in Molossidae
Distribution. Known originally from only type locality in S Andean Peru but recently also found in a second locality in Santuario historico de Machu Picchu.
Recent population differentiation in the habitat specialist Glossy Antshrike (Aves: Thamnophilidae) across Amazonian seasonally flooded forests: Complete matrix
<p>We assessed population structure and the spatio-temporal pattern of diversification in the Glossy Antshrike <i>Sakesphorus luctuosus</i> (Aves, Thamnophilidae) to understand the processes shaping the evolutionary history of Amazonian floodplains and address unresolved taxonomic controversies surrounding its species limits. By targeting ultraconserved elements (UCEs) from 32 specimens of <i>S. luctuosus</i>, we identified independent lineages and estimated their differentiation, divergence times and migration rates. We also estimated current and past demographic histories for each recovered lineage. We found evidence confirming that <i>S. luctuosus</i> consists of a single species, comprising at least four populations, with some highly admixed individuals and overall similar levels of migration between populations. We confirmed the differentiation of the Araguaia River basin population (<i>S. l.</i> <i>araguayae</i>), and gathered circumstantial evidence indicating that the taxon <i>S. hagmanni</i> may represent a highly introgressed population between 3 distinct phylogroups of <i>S. luctuosus</i>. Divergence time estimates between populations seem to be recent, occurring during the last 183 kya. Signs of population expansions were detected for populations attributed to subspecies <i>S. l. luctuosus</i>, but the <i>S. l. araguayae </i>population had probably maintained its effective size through time. Our results support<b> </b>that <i>S. luctuosus</i> has had a complex population history, resulting from a high dependence on southeastern "clear-water" habitats and their availability through time. Spatial and demographic expansions towards the western "white water" flooded forests might still be ongoing. Our study reinforces the view that isolation due to absence of suitable habitat has been an important driver of population differentiation within Amazonian flooded forests, but also that differences between <i>várzeas</i> ("white water" floodplains, mostly in southwestern Amazonia) and <i>igapós</i> ("clear- water" floodplains, especially located in the east) should be further explored as powerful drivers of micro-evolution.</p>
Distribution. Presumably endemic to mountains of Cameroon; known from type locality, Bamenda Highlands, and more recently from Mt Oku. in Soricidae
Distribution. Presumably endemic to mountains of Cameroon; known from type locality, Bamenda Highlands, and more recently from Mt Oku.
Distribution. NE of DR Congo, and possibly restricted to this region; known from type locality, Ituri Forest, and Medje. Recently it has been reported from Okapi Wildlife Reserve and Masako Forest. in Soricidae
Distribution. NE of DR Congo, and possibly restricted to this region; known from type locality, Ituri Forest, and Medje. Recently it has been reported from Okapi Wildlife Reserve and Masako Forest.
Distribution. NE Mali, EC & SE Sudan, SE South Sudan, and NE Ethiopia. There is also a record from ancient Egypt in Thebes where a mummified individual has recently been identified, although status of the species there is uncertain considering no individuals have been observed there in recent times. in Soricidae
Distribution. NE Mali, EC & SE Sudan, SE South Sudan, and NE Ethiopia. There is also a record from ancient Egypt in Thebes where a mummified individual has recently been identified, although status of the species there is uncertain considering no individuals have been observed there in recent times.
Distribution. Uncertain, but the type locality is generally accepted to be Mt Kilimanjaro, NE Tanzania; there are further reports of this species throughout W & E Africa (including some recent ones from Uganda), but they cannot be confirmed since most of the specimens have been wrongly attributed. in Soricidae
Distribution. Uncertain, but the type locality is generally accepted to be Mt Kilimanjaro, NE Tanzania; there are further reports of this species throughout W & E Africa (including some recent ones from Uganda), but they cannot be confirmed since most of the specimens have been wrongly attributed.
Distribution. Near Halabiya at the Euphrates and Qal'at Sukkara (Syria); potentially in SW Iran. There are no recent records from Israel, Palestine or Lebanon indicating that the species is potentially extinct in this region. However, it cannot certainly be excluded that katinka is more common in the Levant and the Arabian Peninsula. in Soricidae
Distribution. Near Halabiya at the Euphrates and Qal'at Sukkara (Syria); potentially in SW Iran. There are no recent records from Israel, Palestine or Lebanon indicating that the species is potentially extinct in this region. However, it cannot certainly be excluded that katinka is more common in the Levant and the Arabian Peninsula.
Distribution. Known only from living specimens in Giza, Nile Delta, NE Egypt, plus a recent additional record S on the Nile and another to the N of Giza in the Nile Delta; mummified specimens are known from Thebes, SE Egypt; it may have a more extensive distribution throughout the Nile Valley between Giza and Thebes. in Soricidae
Distribution. Known only from living specimens in Giza, Nile Delta, NE Egypt, plus a recent additional record S on the Nile and another to the N of Giza in the Nile Delta; mummified specimens are known from Thebes, SE Egypt; it may have a more extensive distribution throughout the Nile Valley between Giza and Thebes.
Subspecies and Distribution. C.r.russulaHermann,1780—W&SWEuropeinGermany,Belgium,Netherlands,Luxembourg,N&WSwitzerland,France,Spain,Portugal,andmanycloseoffshoreislands.ApopulationhasbecomeestablishedonGranCanariaIintheCanaryIs,althoughwhenthespecieswaslikelyintroducedisunresolved. C. r. yebalensis Cabrera, 1913 — NW Africa in N Morocco and N Algeria. The Greater White-toothed Shrew has also been recently reported in S Ireland, where it was likely recently introduced, probably representing the subspecies russula. They also seem to have made it to Scilly Is and the Channel Is, where they probably traveled by boat. in Soricidae
Subspecies and Distribution. C.r.russulaHermann,1780—W&SWEuropeinGermany,Belgium,Netherlands,Luxembourg,N&WSwitzerland,France,Spain,Portugal,andmanycloseoffshoreislands.ApopulationhasbecomeestablishedonGranCanariaIintheCanaryIs,althoughwhenthespecieswaslikelyintroducedisunresolved. C. r. yebalensis Cabrera, 1913 — NW Africa in N Morocco and N Algeria. The Greater White-toothed Shrew has also been recently reported in S Ireland, where it was likely recently introduced, probably representing the subspecies russula. They also seem to have made it to Scilly Is and the Channel Is, where they probably traveled by boat.
Distribution. Known only from the Konteh Area of the Sanetti Plateau in SC Ethiopia; it remains possible that this recently described species inhabits other parts of the plateau as well, although it is likely endemic to the Bale Mts. in Soricidae
Distribution. Known only from the Konteh Area of the Sanetti Plateau in SC Ethiopia; it remains possible that this recently described species inhabits other parts of the plateau as well, although it is likely endemic to the Bale Mts.
Distribution. Known from SW China (Yunnan and Guizhou), adjacent N & W Myanmar, Laos, Thailand, and S Vietnam. Because both the Indochinese White-toothed Shrew and the Hainan White-toothed Shrew (C. wuchihensis) were identified as Horsfield's White-toothed Shrew (C. horsfieldiz) until recently, their distribution limits in China are not clear. in Soricidae
Distribution. Known from SW China (Yunnan and Guizhou), adjacent N & W Myanmar, Laos, Thailand, and S Vietnam. Because both the Indochinese White-toothed Shrew and the Hainan White-toothed Shrew (C. wuchihensis) were identified as Horsfield's White-toothed Shrew (C. horsfieldiz) until recently, their distribution limits in China are not clear.
Distribution. Islands off peninsular Thailand (Koh Samui) and Peninsular Malaysia (Tioman, and Mapur); one old specimen from Mt Tahan, Pahang State, Malaysia, might also belong to this species, but no recent confirmation of this taxon on the Malay Peninsula cast doubts about the existence of such a continental population of Peninsular White-toothed Shrew. in Soricidae
Distribution. Islands off peninsular Thailand (Koh Samui) and Peninsular Malaysia (Tioman, and Mapur); one old specimen from Mt Tahan, Pahang State, Malaysia, might also belong to this species, but no recent confirmation of this taxon on the Malay Peninsula cast doubts about the existence of such a continental population of Peninsular White-toothed Shrew.
Distribution. Endemic to Japan, widely distributed on Honshu and Kyushu. No recent records of extant distribution but fossil records found on Shikoku. in Soricidae
Distribution. Endemic to Japan, widely distributed on Honshu and Kyushu. No recent records of extant distribution but fossil records found on Shikoku.
Distribution. Known from Nepal and NE India (Sikkim). Distributional limits remain unclarified because it recently has been elevated to full species. in Soricidae
Distribution. Known from Nepal and NE India (Sikkim). Distributional limits remain unclarified because it recently has been elevated to full species.
Distribution. West Africa, from SE Sierra Leone and S Guinea to Ghana (extending just E of the Volta River), and in S Togo, S Benin, and S Nigeria (S bank of the River Benue just above its confluence with the Niger River in the Idah, Kogi State, and the lower Niger). There is a discontinuity in the distribution between the VoltaRiver in Ghana and the Nigerian population, and it is believed that its range was far greater in the recent past. in Cercopithecidae
Distribution. West Africa, from SE Sierra Leone and S Guinea to Ghana (extending just E of the Volta River), and in S Togo, S Benin, and S Nigeria (S bank of the River Benue just above its confluence with the Niger River in the Idah, Kogi State, and the lower Niger). There is a discontinuity in the distribution between the VoltaRiver in Ghana and the Nigerian population, and it is believed that its range was far greater in the recent past.
Distribution. SE coastal Kenya, confined to a narrow stretch of forest along the lower Tana River, mainly from Garsen N nearly as far as Wenje; recently also found in the forests of the Tana River Delta. in Cercopithecidae
Distribution. SE coastal Kenya, confined to a narrow stretch of forest along the lower Tana River, mainly from Garsen N nearly as far as Wenje; recently also found in the forests of the Tana River Delta.
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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.