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6,383 results for “isolates”
Distribution. EC & SE Brazil (Bahia, Minas Gerais, and Sao Paulo states, and Distrito Federal), with an isolated record in W Brazil (Rondonia State); range may extend to Matto Grosso State. in Cricetidae
Distribution. EC & SE Brazil (Bahia, Minas Gerais, and Sao Paulo states, and Distrito Federal), with an isolated record in W Brazil (Rondonia State); range may extend to Matto Grosso State.
Subspecies and Distribution. N. ¢c. concolor Harlan, 1826 — S China (C & SW Yunnan Province) including a small population W of the Mekong River near the Myanmar border, and N Vietnam (Lao Cai, Son La, and Yen Bai provinces) between the Black and Red rivers from ¢.20° N 023° 45° N. c. c. lu Delacour, 1951 — NW Laos (Bokeo and Luang Namtha provinces) in an isolated population E of the Mekong River at ¢.20° 17° N-20° 25' N. in Hylobatidae
Subspecies and Distribution. N. ¢c. concolor Harlan, 1826 — S China (C & SW Yunnan Province) including a small population W of the Mekong River near the Myanmar border, and N Vietnam (Lao Cai, Son La, and Yen Bai provinces) between the Black and Red rivers from ¢.20° N 023° 45° N. c. c. lu Delacour, 1951 — NW Laos (Bokeo and Luang Namtha provinces) in an isolated population E of the Mekong River at ¢.20° 17° N-20° 25' N.
Distribution. Bangladesh and NE India (states of Assam, Arunachal Pradesh, Nagaland, Meghalaya, Manipur, Mizoram, and Tripura) between the Brahmaputra and Salween rivers, and to the S of the Brahmaputra and E of the Dibang rivers, extending into NW Myanmar, W of the Chindwin River. W. Bleisch has reported an isolated population of gibbons to the N, in the Medog Nature Reserve in SE Xizang Autonomous Region (= Tibet), across the border from Arunachal Pradesh, but their identity has not been established. in Hylobatidae
Distribution. Bangladesh and NE India (states of Assam, Arunachal Pradesh, Nagaland, Meghalaya, Manipur, Mizoram, and Tripura) between the Brahmaputra and Salween rivers, and to the S of the Brahmaputra and E of the Dibang rivers, extending into NW Myanmar, W of the Chindwin River. W. Bleisch has reported an isolated population of gibbons to the N, in the Medog Nature Reserve in SE Xizang Autonomous Region (= Tibet), across the border from Arunachal Pradesh, but their identity has not been established.
Distribution. Patchily distributed on E side of Great Dividing Range from N of Brisbane, Queensland, to Kangaroo Valley, New South Wales. Small isolated populations persist W of the Great Dividing Range in N New South Wales (in the Warrumbungles and at Mt Kaputar) and in E Victoria (East Gippsland). in Macropodidae
Distribution. Patchily distributed on E side of Great Dividing Range from N of Brisbane, Queensland, to Kangaroo Valley, New South Wales. Small isolated populations persist W of the Great Dividing Range in N New South Wales (in the Warrumbungles and at Mt Kaputar) and in E Victoria (East Gippsland).
Distribution. USA and Mexico, from S Nebraska, SE Colorado, and SE Arizona E to Virginia, the Carolinas, Georgia, and Florida, and S through Texas to Nuevo Leon and Tamaulipas, with an isolated population in the lower Colorado River of SW Arizona, SE California, and extreme NW Sonora. in Cricetidae
Distribution. USA and Mexico, from S Nebraska, SE Colorado, and SE Arizona E to Virginia, the Carolinas, Georgia, and Florida, and S through Texas to Nuevo Leon and Tamaulipas, with an isolated population in the lower Colorado River of SW Arizona, SE California, and extreme NW Sonora.
Subspecies and Distribution. M.m.mexicanusSaussure,1861—highplateauregionofCMexico. M.m.fulviventerMerriam,1898—COaxaca,Mexico. M.m.fundatusHall,1948—CMichoacan,Mexico. M.m.madrensisGoldman,1938—SierraMadreOccidental,Chihuahua,Mexico. M.m.neveriaeHooper,1955—SierradeManantlan,Jalisco,2500m. M.m.ocotensisAlvarez&Hernandez-Chavez,1993—ElOcoteVolcano,WChiapas,Mexico. M.m.phaeusMerriam,1892—fromNWDurangoStoNevadodeColima,SJalisco,Mexico. M.m.salvusHall,1948—SierradeTancitaro,Michoacan,Mexico,atelevationsof2400-3500m. M. m. subsimus Goldman, 1938 — isolated mountains from Sierra de Guadalupe in SE Coahuila S through Nuevo Leon to SW Tamaulipas, Mexico. in Cricetidae
Subspecies and Distribution. M.m.mexicanusSaussure,1861—highplateauregionofCMexico. M.m.fulviventerMerriam,1898—COaxaca,Mexico. M.m.fundatusHall,1948—CMichoacan,Mexico. M.m.madrensisGoldman,1938—SierraMadreOccidental,Chihuahua,Mexico. M.m.neveriaeHooper,1955—SierradeManantlan,Jalisco,2500m. M.m.ocotensisAlvarez&Hernandez-Chavez,1993—ElOcoteVolcano,WChiapas,Mexico. M.m.phaeusMerriam,1892—fromNWDurangoStoNevadodeColima,SJalisco,Mexico. M.m.salvusHall,1948—SierradeTancitaro,Michoacan,Mexico,atelevationsof2400-3500m. M. m. subsimus Goldman, 1938 — isolated mountains from Sierra de Guadalupe in SE Coahuila S through Nuevo Leon to SW Tamaulipas, Mexico.
Distribution. Known from relatively few sites in semi-isolated mountain range in Ixtlan District, Oaxaca State, Mexico, that is bounded to N by Rio Santo Domingo, to W & S by Rio Grande, and to E by coastal plain of Gulf of Mexico. in Cricetidae
Distribution. Known from relatively few sites in semi-isolated mountain range in Ixtlan District, Oaxaca State, Mexico, that is bounded to N by Rio Santo Domingo, to W & S by Rio Grande, and to E by coastal plain of Gulf of Mexico.
Distribution. Restricted to three small isolated areas of S Siberia (NE Buryatia and N Zabaykalsky Krai): N Barguzin River, Lake Baunt, and Lower Muya River hollows. in Cricetidae
Distribution. Restricted to three small isolated areas of S Siberia (NE Buryatia and N Zabaykalsky Krai): N Barguzin River, Lake Baunt, and Lower Muya River hollows.
Distribution. Subdivided into several isolated patches of different size: N sections located along Arctic shore in Russia from Northern Dvina River E to Kolyma River (Arkhangelsk Region, Nenets Autonomous District, SE Novaya Zemlya, Vaygach I, Northern Ural Mts, Yamal Peninsula, Belyy I, S Taymyr Peninsula, and N Yakutia), C section includes C Yakutia, and S sections extend from Kama River E to Amur River and from S Siberia S to Tian Shan and interfluve of Huang He and Yangtze in E China including Russia, Kazakhstan, Kyrgyzstan, Mongolia, and China (NW Xinjiang, Inner Mongolia [= Nei Mongol], Heilongjiang, Hebei, and Henan). in Cricetidae
Distribution. Subdivided into several isolated patches of different size: N sections located along Arctic shore in Russia from Northern Dvina River E to Kolyma River (Arkhangelsk Region, Nenets Autonomous District, SE Novaya Zemlya, Vaygach I, Northern Ural Mts, Yamal Peninsula, Belyy I, S Taymyr Peninsula, and N Yakutia), C section includes C Yakutia, and S sections extend from Kama River E to Amur River and from S Siberia S to Tian Shan and interfluve of Huang He and Yangtze in E China including Russia, Kazakhstan, Kyrgyzstan, Mongolia, and China (NW Xinjiang, Inner Mongolia [= Nei Mongol], Heilongjiang, Hebei, and Henan).
Distribution. Restricted to three small isolated areas in the lower Amur River Basin of Russian Far East (Upper Bureya River Depression, Chukchagyr-Evoron lakes Depression, adjacent parts of Amgun River Valley, and Upper Zeya River Depression). in Cricetidae
Distribution. Restricted to three small isolated areas in the lower Amur River Basin of Russian Far East (Upper Bureya River Depression, Chukchagyr-Evoron lakes Depression, adjacent parts of Amgun River Valley, and Upper Zeya River Depression).
Distribution. Restricted to Mauritius; there are two isolated records attributed to this species from the Durban region on E coast of South Africa. Previous authors considered it to occur on Madagascar, but Goodman and coworkers found no evidence for its occurrence there. in Molossidae
Distribution. Restricted to Mauritius; there are two isolated records attributed to this species from the Durban region on E coast of South Africa. Previous authors considered it to occur on Madagascar, but Goodman and coworkers found no evidence for its occurrence there.
Distribution. Restricted to Réunion I; there is an isolated record from S Ethiopia, some several hundred kilometers from the coast. This record represents a vagrant or introduced individual, and the species does not normally occur in Africa. in Molossidae
Distribution. Restricted to Réunion I; there is an isolated record from S Ethiopia, some several hundred kilometers from the coast. This record represents a vagrant or introduced individual, and the species does not normally occur in Africa.
Data from: Premating isolation is determined by larval rearing substrates in cactophilic Drosophila mojavensis. X. Age-specific dynamics of adult epicuticular hyrdocarbon expression in response to different host plants
Analysis of sexual selection and sexual isolation in Drosophila mojavensis and its relatives has revealed a pervasive role of rearing substrates on adult courtship behavior when flies were reared on fermenting cactus in preadult stages. Here, we assessed expression of contact pheromones comprised of epicuticular hydrocarbons (CHCs) from eclosion to 28 days of age in adults from two populations reared on fermenting tissues of two host cacti over the entire life cycle. Flies were never exposed to laboratory food and showed significant reductions in average CHC amounts consistent with CHCs of wild-caught flies. Overall, total hydrocarbon amounts increased from eclosion to 14–18 days, well past age at sexual maturity, and then declined in older flies. Most flies did not survive past 4 weeks. Baja California and mainland populations showed significantly different age-specific CHC profiles where Baja adults showed far less age-specific changes in CHC expression. Adults from populations reared on the host cactus typically used in nature expressed more CHCs than on the alternate host. MANCOVA with age as the covariate for the first six CHC principal components showed extensive differences in CHC composition due to age, population, cactus, sex, and age × population, age × sex, and age × cactus interactions. Thus, understanding variation in CHC composition as adult D. mojavensis age requires information about population and host plant differences, with potential influences on patterns of mate choice, sexual selection, and sexual isolation, and ultimately how these pheromones are expressed in natural populations. Studies of drosophilid aging in the wild are badly needed.
16s rRNA and copLAB partial sequences of copper resistant Xanthomonas spp. isolated from agrochemical impacted crucifer fields in Trinidad
<p>Sanger sequence generated partial sequences of copLAB genes present in copper resistant Xanthomonas spp associated with leaf lesion and 16s rRNA sequences used for bacterial genera identification. Part of an upcoming manuscript, will be linked within document.</p>
Distribution. Arabian Peninsula (SW Saudi Arabia and Yemen) and patchily distributed in Africa from E Sudan, Djibouti, and Ethiopia S to E DR Congo, E Zambia, Malawi, and NW Mozambique, also on Unguja and Mafia Is (Zanzibar Archipelago) and isolated localities in NE Nigeria, Chad, and on the coast of the Republic of Congo. in Pteropodidae
Distribution. Arabian Peninsula (SW Saudi Arabia and Yemen) and patchily distributed in Africa from E Sudan, Djibouti, and Ethiopia S to E DR Congo, E Zambia, Malawi, and NW Mozambique, also on Unguja and Mafia Is (Zanzibar Archipelago) and isolated localities in NE Nigeria, Chad, and on the coast of the Republic of Congo.
Distribution. From Senegal and Gambia through sub-Saharan Africa E to S Chad, Central African Republic, Sudan, South Sudan, extreme NE DR Congo, and Uganda to W Ethiopia, S to Gabon, S Republic of the Congo, and W DR Congo, also some isolated patches in S DR Congo and WC Angola. in Pteropodidae
Distribution. From Senegal and Gambia through sub-Saharan Africa E to S Chad, Central African Republic, Sudan, South Sudan, extreme NE DR Congo, and Uganda to W Ethiopia, S to Gabon, S Republic of the Congo, and W DR Congo, also some isolated patches in S DR Congo and WC Angola.
From Networked to Isolated: Observing Water Hydrogen Bonds in Concentrated Electrolytes with Two Dimensional Infrared Spectroscopy
<p>The files contain the data that are shown in the figures of the Main Text and of the Supplementary Materials of the research article:</p> <p>From Networked to Isolated: Observing Water Hydrogen Bonds in Concentrated Electrolytes with Two Dimensional Infrared Spectroscopy</p> <p>Nicholas H. C. Lewis, Bogdan Dereka, Yong Zhang, Edward J. Maginn, and Andrei Tokmakoff</p> <p>J. Phys. Chem. B, (2022)</p>
FIGURE. Distribution of Dicorynia. Physical map of the Amazonian region with all analyzed specimens of Dicorynia. A large amount of point overlays leading to reduced number of visible points is due to the large percentage of materials being old collections that rely only on the name of the municipality or similar. Source: NASA with modifications. Note that almost all specimens are contained in areas with less than 200 m high and the high elevations of the Guiana shield may represent a form of isolation between the two species. in A Taxonomic Revision of the Amazonian Genus Dicorynia (Fabaceae: Dialioideae)
FIGURE. Distribution of Dicorynia. Physical map of the Amazonian region with all analyzed specimens of Dicorynia. A large amount of point overlays leading to reduced number of visible points is due to the large percentage of materials being old collections that rely only on the name of the municipality or similar. Source: NASA with modifications. Note that almost all specimens are contained in areas with less than 200 m high and the high elevations of the Guiana shield may represent a form of isolation between the two species.
Distribution. Northern Iberian Peninsula, discontinuously from Galicia and N Portugal (N of upper Mondego River) E to both sides of the Pyrenees, also in W Central System and N Iberian System Mts; two small isolated populations in Zézere River (Portugal) and Mayor River (Vizcaya, Spain). in Talpidae
Distribution. Northern Iberian Peninsula, discontinuously from Galicia and N Portugal (N of upper Mondego River) E to both sides of the Pyrenees, also in W Central System and N Iberian System Mts; two small isolated populations in Zézere River (Portugal) and Mayor River (Vizcaya, Spain).
Distribution. Japan (Honshu, Shikoku, and Kyushu); distribution in C Honshu is rather continuous, while N & W distribution is patchy and isolated due to mountainous topography. in Talpidae
Distribution. Japan (Honshu, Shikoku, and Kyushu); distribution in C Honshu is rather continuous, while N & W distribution is patchy and isolated due to mountainous topography.
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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.