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3,145 results for “Well Being”
Data set for: Effects of microstructure evolution on compressive strength of silica sand-enhanced oil well cement at a wide temperature range
<p><span>The influence of microstructure of silica-enhanced cement on the mechanical performance of cement is difficult to be described. In this study, we used the scanning electron microscope and image processing method to investigate the relationship between the complicity of cement microstructure and compressive strength under various temperature and curing time conditions. Fractal dimension was applied to describe the complicity of cement. The relationships among compressive strength, fractal dimension, temperature, curing time and pore structure of cement were identified. The results show that curing time of cement directly control the complicity of cement microstructure and compressive strength by altering the pore orientation and macropore ratio in cement. The curing temperature affects the complicity of cement microstructure and compressive strength indirectly by changing the ratio of micropore and small pore. The fractal dimension of silica-enhanced cement shows good correlation with compressive strength. Pore size distribution is the most important factor that influence the complicity of cement matrix and compressive strength of silica-enhanced cement. When building up the macroscopic mechanical performance model of cement, we should consider the influence of pore size distribution in cement under different curing temperatures and times on the complicity of cement microstructure. </span></p>
Distribution. Mountains of EC DR Congo, Rwanda, and Burundi as well as the Bwindi Impenetrable National Park in extreme SW Uganda and Idjwi I in L Kivu. in Soricidae
Distribution. Mountains of EC DR Congo, Rwanda, and Burundi as well as the Bwindi Impenetrable National Park in extreme SW Uganda and Idjwi I in L Kivu.
Distribution. SE Cameroon, S Central African Republic, N Republic of the Congo, N & E DR Congo, Uganda, Rwanda, Burundi, W Kenya, and Tanzania, and as well as a single record each from S South Sudan and SW Ethiopia; distributional limits of Hildegarde's White-toothed Shrew are still uncertain. in Soricidae
Distribution. SE Cameroon, S Central African Republic, N Republic of the Congo, N & E DR Congo, Uganda, Rwanda, Burundi, W Kenya, and Tanzania, and as well as a single record each from S South Sudan and SW Ethiopia; distributional limits of Hildegarde's White-toothed Shrew are still uncertain.
Distribution. SE Nigeria, Cameroon, S Central African Republic, N Gabon, N Republic of the Congo, N DR Congo, and WC Uganda as well as a disjunctset of records from Guinea and Sierra Leone. in Soricidae
Distribution. SE Nigeria, Cameroon, S Central African Republic, N Gabon, N Republic of the Congo, N DR Congo, and WC Uganda as well as a disjunctset of records from Guinea and Sierra Leone.
Distribution. SE Kenya and NE Tanzania, as well as a disjunct record from NW Kenya, although this specimen needs to be further examined for misidentification. in Soricidae
Distribution. SE Kenya and NE Tanzania, as well as a disjunct record from NW Kenya, although this specimen needs to be further examined for misidentification.
Distribution. Jombeni Range near Nyeri in WC Kenya; potentially found in the Aberdare Range as well, although this has yet to be confirmed. in Soricidae
Distribution. Jombeni Range near Nyeri in WC Kenya; potentially found in the Aberdare Range as well, although this has yet to be confirmed.
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. Endemic to the Ryukyu Is, including 15 small islands of both the Amami and Okinawa Is; it may be distributed to the other small islands as well. in Soricidae
Distribution. Endemic to the Ryukyu Is, including 15 small islands of both the Amami and Okinawa Is; it may be distributed to the other small islands as well.
Distribution. SE Nigeria (Obudu Plateau), S Cameroon, SW Central African Republic, Equatorial Guinea, and Gabon, as well as one record from SE DR Congo; possibly W Republic of the Congo. in Soricidae
Distribution. SE Nigeria (Obudu Plateau), S Cameroon, SW Central African Republic, Equatorial Guinea, and Gabon, as well as one record from SE DR Congo; possibly W Republic of the Congo.
Distribution. SE DR Congo and W Tanzania S through E Zambia, W Malawi, W Mozambique, and E Zimbabwe to South Africa and Lesotho, as well as a single isolated record from C Nigeria; most records throughoutits distribution are scattered. in Soricidae
Distribution. SE DR Congo and W Tanzania S through E Zambia, W Malawi, W Mozambique, and E Zimbabwe to South Africa and Lesotho, as well as a single isolated record from C Nigeria; most records throughoutits distribution are scattered.
Distribution. Throughout sub-Saharan Africa from Guinea E to W Kenya and S to C Mozambique and C Angola, as well as an isolated region of W Ethiopia. in Soricidae
Distribution. Throughout sub-Saharan Africa from Guinea E to W Kenya and S to C Mozambique and C Angola, as well as an isolated region of W Ethiopia.
Distribution. SE Coahuila and W Nuevo Leon as well as a disjunct population in NW Coahuila, NE Mexico. in Soricidae
Distribution. SE Coahuila and W Nuevo Leon as well as a disjunct population in NW Coahuila, NE Mexico.
Distribution. Great Basin in EC California and SW Nevada as well as an isolated record from WC Utah (SW USA). in Soricidae
Distribution. Great Basin in EC California and SW Nevada as well as an isolated record from WC Utah (SW USA).
Distribution. WC USA from Montana S through Wyoming, SW South Dakota, extreme NW Nebraska, Utah, Colorado, Utah, Arizona, and New Mexico; probably SE Idaho as well. in Soricidae
Distribution. WC USA from Montana S through Wyoming, SW South Dakota, extreme NW Nebraska, Utah, Colorado, Utah, Arizona, and New Mexico; probably SE Idaho as well.
Distribution. Borneo, confined to an area of E Kalimantan, from the Kayan and Sembakung (= Sebuku) rivers in the N, S, and SW to the Mahakam River, the W boundary is not well known but certainly E of the Apau Kayan and the Kayan Mentarang National Park. in Cercopithecidae
Distribution. Borneo, confined to an area of E Kalimantan, from the Kayan and Sembakung (= Sebuku) rivers in the N, S, and SW to the Mahakam River, the W boundary is not well known but certainly E of the Apau Kayan and the Kayan Mentarang National Park.
Distribution. From Senegal and Guinea-Bissau (including the Bijagos Archipelago), E to just W of the Volta River system in Ghana; possibly also in S Mauritania. Introduced into the Cape Verde and Canary Is, as well as to Barbados, Nevis, and Saint Kitts Is in the West Indies. in Cercopithecidae
Distribution. From Senegal and Guinea-Bissau (including the Bijagos Archipelago), E to just W of the Volta River system in Ghana; possibly also in S Mauritania. Introduced into the Cape Verde and Canary Is, as well as to Barbados, Nevis, and Saint Kitts Is in the West Indies.
Subspecies and Distribution. R.c.fuscipesWaterhouse,1839—SWWesternAustraliaaswellasvariousoffshoreIs. R.c.asstmilisGould,1858—EVictoriaandSEQueenslandandsomeoffshoreIs. R.c.coraciusThomas,1923—NEQueensland,includingHinchinbrook I. R. c. greyi Gray, 1841 — SE South Australia and SW Victoria as well as various offshore Is including Kangaroo I. in Muridae
Subspecies and Distribution. R.c.fuscipesWaterhouse,1839—SWWesternAustraliaaswellasvariousoffshoreIs. R.c.asstmilisGould,1858—EVictoriaandSEQueenslandandsomeoffshoreIs. R.c.coraciusThomas,1923—NEQueensland,includingHinchinbrook I. R. c. greyi Gray, 1841 — SE South Australia and SW Victoria as well as various offshore Is including Kangaroo I.
Distribution. Most of India, Nepal, Bang- ladesh, SC & SE China (Sichuan, Yunnan, Guizhou, Guangdong, and Fujian) and mainland SE Asia (Myanmar, Thailand, Laos, Vietnam, and Cambodia), also on Cat Ba I off the coast of N Vietnam. Popu- lation of Taiwan has uncertain origins. Introduced into Kedah and Perlis regions of Malay Peninsula as well as Java. in Muridae
Distribution. Most of India, Nepal, Bang- ladesh, SC & SE China (Sichuan, Yunnan, Guizhou, Guangdong, and Fujian) and mainland SE Asia (Myanmar, Thailand, Laos, Vietnam, and Cambodia), also on Cat Ba I off the coast of N Vietnam. Popu- lation of Taiwan has uncertain origins. Introduced into Kedah and Perlis regions of Malay Peninsula as well as Java.
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008). in Muridae
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008).
Distribution. Present in most of mainland New Guinea, as well as a number ofislands in the Raja Ampat Is (Batanta), Cenderawasih (= Geelvink) Bay (Yapen and Biak), and the Bismarck Archipelago (New Britain) and D'Entrecasteaux Is (Goodenough, Fergusson, and Normanby). in Muridae
Distribution. Present in most of mainland New Guinea, as well as a number ofislands in the Raja Ampat Is (Batanta), Cenderawasih (= Geelvink) Bay (Yapen and Biak), and the Bismarck Archipelago (New Britain) and D'Entrecasteaux Is (Goodenough, Fergusson, and Normanby).
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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.