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Distribution. SE Brazil (in the states of Espirito Santo, neighboring E Minas Gerais, and extreme N Rio de Janeiro), the distribution may be at least partly limited by the Rio Jequitinhonha to the N, but probably intergrades with distributions of the Blackfronted Titi (C. nigrifrons) to the S and W and the Southern Bahian Titi (C. melanochir) to the N. The exact present-day limits of the distribution of C. personatus are unclear. in Phitheciidae
Distribution. SE Brazil (in the states of Espirito Santo, neighboring E Minas Gerais, and extreme N Rio de Janeiro), the distribution may be at least partly limited by the Rio Jequitinhonha to the N, but probably intergrades with distributions of the Blackfronted Titi (C. nigrifrons) to the S and W and the Southern Bahian Titi (C. melanochir) to the N. The exact present-day limits of the distribution of C. personatus are unclear.
Distribution. Brazilian Amazon, S of the Rio Amazonas, between the Tapajos/Juruena system and the Tocantins/Araguaia river system to the E, in the Brazilian states of Para and Mato Grosso; the exact S limit ofits distribution is unclear, but it seems likely that it coincides with the transition between the Amazon rainforest and the cerrado savannas of C Brazil; this ecotone encompasses headwaters of the Xingu and Tapajos river systems in N Mato Grosso. Vieira's Titi (C. vieirai) is also known to occur in this region, but there are too few records to confirm whether their distributions intergrade, or in fact where the exact limits of their distributions are. One recent study also found that the Red-bellied Titi may be absent from or present at extremely low densities in large areas of the Tocantins-Xingu interfluvium. Given the overall lack of records, while it is clear that the Red-bellied Titi occurs over a vast area of the SE Amazon Basin, the exact limits of its distribution within this area remain unclear. in Phitheciidae
Distribution. Brazilian Amazon, S of the Rio Amazonas, between the Tapajos/Juruena system and the Tocantins/Araguaia river system to the E, in the Brazilian states of Para and Mato Grosso; the exact S limit ofits distribution is unclear, but it seems likely that it coincides with the transition between the Amazon rainforest and the cerrado savannas of C Brazil; this ecotone encompasses headwaters of the Xingu and Tapajos river systems in N Mato Grosso. Vieira's Titi (C. vieirai) is also known to occur in this region, but there are too few records to confirm whether their distributions intergrade, or in fact where the exact limits of their distributions are. One recent study also found that the Red-bellied Titi may be absent from or present at extremely low densities in large areas of the Tocantins-Xingu interfluvium. Given the overall lack of records, while it is clear that the Red-bellied Titi occurs over a vast area of the SE Amazon Basin, the exact limits of its distribution within this area remain unclear.
Subspecies and Distribution. D.n.novemcinctusLinnaeus,1758—EColombia,E&SVenezuela,theGuianas,mostofBrazil,EEcuador,EPeru,Bolivia,Paraguay,Uruguay,andN&CEArgentina;alsoonMargarita,Trinidad,Tobago,andGrenadaIs. D.n.aequatorialisL.onnberg,1913—WAndeanslopefromColombiatoNWPeru. D.n.davis:Russell,1953—WMexico,fromNSinaloaStoGuerrerostates. D.n.fenestratusPeters,1864—fromHondurasSEtoPanama(includingBarroColoradoI)andtheNtipofSouthAmericainN&EColombiaandN&WVenezuela. D.n.mexianaeHagmann,1908—AmazonDelta,ParaState,Brazil. D. n. mexicanus Peters, 1864 — C, S & SE USA, E & S Mexico, Belize, and Guatemala. Also present in El Salvador, but subspecies involved not known. in Dasypodidae
Subspecies and Distribution. D.n.novemcinctusLinnaeus,1758—EColombia,E&SVenezuela,theGuianas,mostofBrazil,EEcuador,EPeru,Bolivia,Paraguay,Uruguay,andN&CEArgentina;alsoonMargarita,Trinidad,Tobago,andGrenadaIs. D.n.aequatorialisL.onnberg,1913—WAndeanslopefromColombiatoNWPeru. D.n.davis:Russell,1953—WMexico,fromNSinaloaStoGuerrerostates. D.n.fenestratusPeters,1864—fromHondurasSEtoPanama(includingBarroColoradoI)andtheNtipofSouthAmericainN&EColombiaandN&WVenezuela. D.n.mexianaeHagmann,1908—AmazonDelta,ParaState,Brazil. D. n. mexicanus Peters, 1864 — C, S & SE USA, E & S Mexico, Belize, and Guatemala. Also present in El Salvador, but subspecies involved not known.
Distribution. CE Madagascar, but the geographic distribution is poorly known; at present known only from its type locality of Andasibe (= Périnet) and neighboring areas (e.g. Maromizaha Forest), Analamazaotra Special Reserve, Anjozorobe-Angavo Protected Area, and Mantadia National Park. in Cheirogaleidae
Distribution. CE Madagascar, but the geographic distribution is poorly known; at present known only from its type locality of Andasibe (= Périnet) and neighboring areas (e.g. Maromizaha Forest), Analamazaotra Special Reserve, Anjozorobe-Angavo Protected Area, and Mantadia National Park.
The domain structure of keratin 2 and the mutation detected in the present patient.
<p>The location of the mutation in this patient is indicated by the black arrow.</p>
Distribution. New Guinea, including Yapen, Mios Num, and Roon Is in Cenderawasih (= Geelvink) Bay, Karkar and Walis Is off the N coast, Raja Ampat Is of Salawati, Sorong, and Misool, SE Papua New Guinea Is of Samarai (= Dinner) and Dufaure (= Dufour), and Aru Is. It is present on many islands of C & S Moluccas (Seram, Ambon, Pulau Pandjang, Buru, and the Tayandu and Kai archipelagos). It has been introduced to Selayar I between Sulawesi and Flores (W occurrence of the species), and there are vague records from Flores and Sulawesi, which may also refer to the Selayar population. This species was also apparently introduced to Mussau (St. Matthias Group, NE Bismarck Archipelago) in prehistoric times and to New Ireland I (Bismarck Archipelago) in the 20™ century. in Phalangeridae
Distribution. New Guinea, including Yapen, Mios Num, and Roon Is in Cenderawasih (= Geelvink) Bay, Karkar and Walis Is off the N coast, Raja Ampat Is of Salawati, Sorong, and Misool, SE Papua New Guinea Is of Samarai (= Dinner) and Dufaure (= Dufour), and Aru Is. It is present on many islands of C & S Moluccas (Seram, Ambon, Pulau Pandjang, Buru, and the Tayandu and Kai archipelagos). It has been introduced to Selayar I between Sulawesi and Flores (W occurrence of the species), and there are vague records from Flores and Sulawesi, which may also refer to the Selayar population. This species was also apparently introduced to Mussau (St. Matthias Group, NE Bismarck Archipelago) in prehistoric times and to New Ireland I (Bismarck Archipelago) in the 20™ century.
Distribution. New Guinea, widespread throughout lowlands from the Bird's Head (= Vogelkop) Peninsula in W to Milne Bay Province in E, also present on Salawati and Yapen Is. in Pseudocheiridae
Distribution. New Guinea, widespread throughout lowlands from the Bird's Head (= Vogelkop) Peninsula in W to Milne Bay Province in E, also present on Salawati and Yapen Is.
Distribution. Endemic to N Australia, with two main populations, one in the Kimberley region of Western Australia that extends into W Northern Territory and a second from NC Northern Territory to Boodjamulla (= Lawn Hill) National Park in NW Queensland; also present on Groote Eylandt I. in Pseudocheiridae
Distribution. Endemic to N Australia, with two main populations, one in the Kimberley region of Western Australia that extends into W Northern Territory and a second from NC Northern Territory to Boodjamulla (= Lawn Hill) National Park in NW Queensland; also present on Groote Eylandt I.
Distribution. Endemic to Iberian Peninsula where widespread in NW & W but absent in most of the E, Pyrenees, and Ebro Basin, also present on Cortegada (Galicia) tidal island. in Talpidae
Distribution. Endemic to Iberian Peninsula where widespread in NW & W but absent in most of the E, Pyrenees, and Ebro Basin, also present on Cortegada (Galicia) tidal island.
Distribution. Most of Europe, from the British Is and NW France E to W Siberia as far E as Irtysh and Ob rivers, and from S Sweden, S Finland, and S Karelia (Russia) S to N Italy and N Balkans; marginally present also in NW Kazakhstan. In E Europe and in Asia the border roughly follows the extreme extension of the taiga in the N (northernmost record is from Pechora River close to 68°N) and the steppe-forest—steppe transition in the S. Present on some Is in the Baltic Sea and around Denmark (Oland, Funen, Zeeland, Bjgrng, Tasinge, Tung, Langeland, Riigen, Usedom, and Wollin), around Great Britain (Sky, Mull, Anglesey, Wight, and Jersey), offshore W coast of France (Ouessant and Ré), and on Cres (Croatia) as the only Mediterranean I. in Talpidae
Distribution. Most of Europe, from the British Is and NW France E to W Siberia as far E as Irtysh and Ob rivers, and from S Sweden, S Finland, and S Karelia (Russia) S to N Italy and N Balkans; marginally present also in NW Kazakhstan. In E Europe and in Asia the border roughly follows the extreme extension of the taiga in the N (northernmost record is from Pechora River close to 68°N) and the steppe-forest—steppe transition in the S. Present on some Is in the Baltic Sea and around Denmark (Oland, Funen, Zeeland, Bjgrng, Tasinge, Tung, Langeland, Riigen, Usedom, and Wollin), around Great Britain (Sky, Mull, Anglesey, Wight, and Jersey), offshore W coast of France (Ouessant and Ré), and on Cres (Croatia) as the only Mediterranean I.
Distribution. CE Madagascar, the Mangoro and Onive rivers are the N limits of the present range, and the Rienana River in Andringitra National Park is the S boundary. The former distribution probably extended somewhat N and further S to the Manampatrana River, but populations in those regions appear to have been extirpated. in Indriidae
Distribution. CE Madagascar, the Mangoro and Onive rivers are the N limits of the present range, and the Rienana River in Andringitra National Park is the S boundary. The former distribution probably extended somewhat N and further S to the Manampatrana River, but populations in those regions appear to have been extirpated.
Cuadro del área basal y área basal relativa, calculado para las especies con DAP superior a 3 cm presentes en la cobertura Bosque fragmentado con vegetación secundaria (Bf), sector vereda Larga la vida, Municipio de Dibulla, La Guajira (Colombia). Área basal (G); Área basal relativa (Gr).
<p>Publicado en:</p> <p>Pérez Brito, J., Sierra Julio, M. & Acuña Vargas, J. (2022). Estructura y composición de la vegetación riparia en la cuenca baja de la Quebrada Larga la Vida, municipio de Dibulla, La Guajira (Colombia). <em>Ciencia e Ingeniería</em>, 9 (1): e6711270. https://www.doi.org/10.5281/zenodo.6711270</p>
Distribution. NW Madagascar, the core distribution seems to be to the N and E of the Betsiboka River as far as the Bay of Narinda, and this is also the species present in Ankarafantsika National Park. The isolated population farther N in the Ankarana region may also be this species, but, in between, the Sambirano Woolly Lemur (A. unicolor) inhabits both the Ampasindava Peninsula and the Sambirano region, including the Manongarivo Special Reserve. in Indriidae
Distribution. NW Madagascar, the core distribution seems to be to the N and E of the Betsiboka River as far as the Bay of Narinda, and this is also the species present in Ankarafantsika National Park. The isolated population farther N in the Ankarana region may also be this species, but, in between, the Sambirano Woolly Lemur (A. unicolor) inhabits both the Ampasindava Peninsula and the Sambirano region, including the Manongarivo Special Reserve.
Dataset presented in the recently submitted AGU manuscript "A multi-resolution finite-element approach for global electromagnetic induction modeling with application to southeast China coastal geomagnetic observatory studies"
<p>Dataset presented in the recently submitted AGU paper "A multi-resolution finite-element approach for global electromagnetic induction modeling with application to southeast China coastal geomagnetic observatory studies"</p>
Subspecies and Distribution. D.g.goodfellowiThomas,1908—SEPapuaNewGuinea. D.g.buergersiMatschie,1912—CentralRangeofPapuaNewGuinea. D. g. pulcherrimus Flannery, 1993 — Torricelli Mts and Foja Mts, N New Guinea. An introduced population is present in W New Britain, Bismarck Archipelago. in Macropodidae
Subspecies and Distribution. D.g.goodfellowiThomas,1908—SEPapuaNewGuinea. D.g.buergersiMatschie,1912—CentralRangeofPapuaNewGuinea. D. g. pulcherrimus Flannery, 1993 — Torricelli Mts and Foja Mts, N New Guinea. An introduced population is present in W New Britain, Bismarck Archipelago.
Subspecies and Distribution. P.l.lateralisGould,1842—patchilyacrossSWesternAustralia,includingCapeRange,LittleSandyDesert,andthenearKellerberrininWheatbelt;alsoBarrowIandSalisburyI. P.l.hackettiThomas,1905—islandsofWilson,Mondrain,andWestall(RechercheArchipelago),WesternAustralia.Mayhaveoccurredhistoricallyalsoonadjacentmainland. P. l. pearson: Thomas, 1922 — North Pearson I, Investigator Group, South Australia. Introduced to South and Middle Pearson, Thistle, and Wedge Is, South Australia. A hitherto undescribed subspecies, the West Kimberley race, occurs (distributional limits uncertain) in Edgar, Grant, and Erskine Ranges and on Mt Wynne, Mt Anderson, and Mt Alexander, in S West Kimberley, Western Australia. A second undescribed subspecies, the MacDonnell Ranges race, is present in MacDonnell Ranges of C Australia, extending to E Western Australia and N South Australia. in Macropodidae
Subspecies and Distribution. P.l.lateralisGould,1842—patchilyacrossSWesternAustralia,includingCapeRange,LittleSandyDesert,andthenearKellerberrininWheatbelt;alsoBarrowIandSalisburyI. P.l.hackettiThomas,1905—islandsofWilson,Mondrain,andWestall(RechercheArchipelago),WesternAustralia.Mayhaveoccurredhistoricallyalsoonadjacentmainland. P. l. pearson: Thomas, 1922 — North Pearson I, Investigator Group, South Australia. Introduced to South and Middle Pearson, Thistle, and Wedge Is, South Australia. A hitherto undescribed subspecies, the West Kimberley race, occurs (distributional limits uncertain) in Edgar, Grant, and Erskine Ranges and on Mt Wynne, Mt Anderson, and Mt Alexander, in S West Kimberley, Western Australia. A second undescribed subspecies, the MacDonnell Ranges race, is present in MacDonnell Ranges of C Australia, extending to E Western Australia and N South Australia.
Subspecies and Distribution. M.i.rantThomas,1921—SWIran. M.i.karamaniKrystufeketal.,2010—STurkey,Lebanon,NWSyria,andWIran. M. i. schidlovskii Argyropulo, 1933 — E Turkey, SC Georgia, W Armenia, and NW & N Iran. Also present in Iraq, but subspecies involved not known. in Cricetidae
Subspecies and Distribution. M.i.rantThomas,1921—SWIran. M.i.karamaniKrystufeketal.,2010—STurkey,Lebanon,NWSyria,andWIran. M. i. schidlovskii Argyropulo, 1933 — E Turkey, SC Georgia, W Armenia, and NW & N Iran. Also present in Iraq, but subspecies involved not known.
Subspecies and Distribution. L.m.mandarinusMilne-Edwards,1871—NC&ECChina(SInnerMongolia[=NeiMongol],Shaanxi,Shanxi,Henan,andNEAnhui). L.m.faeceusG.M.Allen,1924—EChina(SEInnerMongolia,Hebei,WLiaoning,Beijing,Shandong,andJiangsu). L.m.johannesThomas,1910—NCChina(NEShanxi). L.m.kishida:Mori,1930—KoreanPeninsula. L. m. vinogradovi Fetisov, 1936 — S Transbaikalia in Russia (S Buryatia) and NC Mongolia. Also present in NE Inner Mongolia, but subspecies involved not known. in Cricetidae
Subspecies and Distribution. L.m.mandarinusMilne-Edwards,1871—NC&ECChina(SInnerMongolia[=NeiMongol],Shaanxi,Shanxi,Henan,andNEAnhui). L.m.faeceusG.M.Allen,1924—EChina(SEInnerMongolia,Hebei,WLiaoning,Beijing,Shandong,andJiangsu). L.m.johannesThomas,1910—NCChina(NEShanxi). L.m.kishida:Mori,1930—KoreanPeninsula. L. m. vinogradovi Fetisov, 1936 — S Transbaikalia in Russia (S Buryatia) and NC Mongolia. Also present in NE Inner Mongolia, but subspecies involved not known.
Distribution. Great Britain, C Europe, and Scandinavia, and across E Europe, Anatolia, Caucasus, NW Iran, and Kazakhstan to Siberia (E to Lake Baikal and Lena River), extreme N Mongolia (Mongolian Altai and Hovsgol Mts), and NE China (N Xinjiang); also present on many islands and islets in Baltic and North seas. in Cricetidae
Distribution. Great Britain, C Europe, and Scandinavia, and across E Europe, Anatolia, Caucasus, NW Iran, and Kazakhstan to Siberia (E to Lake Baikal and Lena River), extreme N Mongolia (Mongolian Altai and Hovsgol Mts), and NE China (N Xinjiang); also present on many islands and islets in Baltic and North seas.
Subspecies and Distribution. n. nivalis Martins, 1842 — Alps. OONDno. abulensis Morales, 1936 — Iberian Peninsula.. aleco Paspalev, V. Martino & Pesheyv, 1952 — E Balkan Peninsula. 9. appenninicus Dal Piaz, 1929 — Italian Peninsula.. cedrorum Spitzenberger, 1973 — Taurus Mts and SW Anatolia, Turkey. 3. dementievi Heptner, 1939 — S Turkmenistan and NE Iran.. hermonis G. S. Miller, 1908 — Lebanon, W & S Syria, and extreme N Israel. OADSs. malyi Bolkay, 1925 — W Balkan Peninsula.. mirhanreini Schafer, 1935 — Tatra Mts in S Poland and Slovakia.. olympus Neuhauser, 1936 — NW Anatolia, N Turkey. 83 £. pontius G. S. Miller, 1908 — NE Anatolia, NE Turkey. n. trialeticus Shidlovsky, 1919 — Caucasus. C. n. ulpius G. S. Miller, 1908 — E & S Carpathian Mts in SW Ukraine and Romania. Also present in S France, S Turkey (Hatay Province), and NW Iran, but subspecies involved not known. in Cricetidae
Subspecies and Distribution. n. nivalis Martins, 1842 — Alps. OONDno. abulensis Morales, 1936 — Iberian Peninsula.. aleco Paspalev, V. Martino & Pesheyv, 1952 — E Balkan Peninsula. 9. appenninicus Dal Piaz, 1929 — Italian Peninsula.. cedrorum Spitzenberger, 1973 — Taurus Mts and SW Anatolia, Turkey. 3. dementievi Heptner, 1939 — S Turkmenistan and NE Iran.. hermonis G. S. Miller, 1908 — Lebanon, W & S Syria, and extreme N Israel. OADSs. malyi Bolkay, 1925 — W Balkan Peninsula.. mirhanreini Schafer, 1935 — Tatra Mts in S Poland and Slovakia.. olympus Neuhauser, 1936 — NW Anatolia, N Turkey. 83 £. pontius G. S. Miller, 1908 — NE Anatolia, NE Turkey. n. trialeticus Shidlovsky, 1919 — Caucasus. C. n. ulpius G. S. Miller, 1908 — E & S Carpathian Mts in SW Ukraine and Romania. Also present in S France, S Turkey (Hatay Province), and NW Iran, but subspecies involved not known.
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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.