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20 results for “water occurence”
Gas exchange, dieback, leaf water potential and chlorophyll content during a greenhouse drought experiment: An evolutionary perspective on functional diversity in co-occuring willow(salix) species
Thirteen willow (Salix) species occur in southeastern Minnesota and often co-occur within the same wetlands. This high local diversity is challenging to explain since closely related species are often functionally similar and density-dependent interactions such as competition and susceptibility to pests and pathogens should limit their co-occurrence. However, if willow species are partitioning resources, or if they are phylogenetically structured so that closely related species rarely co-occur, then the impact of these density-dependent processes could be reduced. In this study, I examined the role of niche partitioning in maintaining local willow diversity by comparing species physiology in a greenhouse.
Collection of chemical occurance data from NORMAN surface water database and other related files
<p>This data set collection includes the downloaded chemical occurrence data from the NORMAN database. It is related with the surface waters. Additionally, this collection also includes the chemical data from the NORMAN database and DSSTox.<br><br>Curated version of this dataset using the newly developed CleanGeoStreamR R package can be found in:<a href="https://zenodo.org/records/13799955"><em> Curated NORMAN Data</em></a>.<br><br>More details about the applied methods and the development of <strong>CleanGeoStreamR</strong> can be found in the following scientific paper: <a href="https://doi.org/10.1016/j.ecoinf.2025.103038"><em>Automated Curation of Spatial Metadata in Environmental Monitoring Data</em></a> (DOI: 10.1016/j.ecoinf.2025.103038).<br><br><br></p>
Distribution. SW Asia from Iraq and Iran to Afghanistan, Pakistan, India, Nepal, and Bhutan; also Bangladesh, Myanmar and S China (including Hainan I). Introduced to Antigua, Barbados, Beef Island, Buck Island, Carriacou, Croatia, Cuba, Fiji, French Guiana, Goat Island, Grenada, Guadeloupe, Guyana, Hawaii, Hispaniola, Jamaica, Japan, Jost Van Dyke, La Desirade, Lavango, Mafia (Tanzania), Marie Galante, Martinique, Maui, Mauritius, Molokai, Nevis, Oahu, Puerto Rico, St. Croix, St. John, St. Kitts, St. Lucia, St. Martin, St. Thomas, St. Vincent, Surinam, Tortola, Trinidad, Vieques, and Water Island. Introduction was unsuccessful in the Dominican Republic. The Small Indian Mongoose or the Javan Mongoose is said to occur on Hong Kong since the 1980s, and to have been also introduced to some Indonesian islands (particularly Ambon). in Herpestidae
Distribution. SW Asia from Iraq and Iran to Afghanistan, Pakistan, India, Nepal, and Bhutan; also Bangladesh, Myanmar and S China (including Hainan I). Introduced to Antigua, Barbados, Beef Island, Buck Island, Carriacou, Croatia, Cuba, Fiji, French Guiana, Goat Island, Grenada, Guadeloupe, Guyana, Hawaii, Hispaniola, Jamaica, Japan, Jost Van Dyke, La Desirade, Lavango, Mafia (Tanzania), Marie Galante, Martinique, Maui, Mauritius, Molokai, Nevis, Oahu, Puerto Rico, St. Croix, St. John, St. Kitts, St. Lucia, St. Martin, St. Thomas, St. Vincent, Surinam, Tortola, Trinidad, Vieques, and Water Island. Introduction was unsuccessful in the Dominican Republic. The Small Indian Mongoose or the Javan Mongoose is said to occur on Hong Kong since the 1980s, and to have been also introduced to some Indonesian islands (particularly Ambon).
Distribution. Cold-temperate waters of the Southern Hemisphere, mainly at 20-60° S except on both coasts of South America, where they occur at most lower latitudes. Concentrated in winter near the coastlines off S Australia, New Zealand, Atlantic coast of South America (Argentina, Brazil), and S Africa (mainly South Africa), but also off Chile, Peru, Tristan da Cunha Is and the E coast of Madagascar; in summer they are found mainly in latitudes of 40-50° S but have been seen in the Antarctic as far as 65° S and around South Georgia Is. in Balaenidae
Distribution. Cold-temperate waters of the Southern Hemisphere, mainly at 20-60° S except on both coasts of South America, where they occur at most lower latitudes. Concentrated in winter near the coastlines off S Australia, New Zealand, Atlantic coast of South America (Argentina, Brazil), and S Africa (mainly South Africa), but also off Chile, Peru, Tristan da Cunha Is and the E coast of Madagascar; in summer they are found mainly in latitudes of 40-50° S but have been seen in the Antarctic as far as 65° S and around South Georgia Is.
Distribution. Cosmopolitan in temperate and tropical waters of the Atlantic, Pacific, and Indian oceans; concentrations of stranding records occur along E USA, South Africa, and New Zealand and to a lesser degree on French and Spanish coasts; precise at-sea distribution is unknown. in Kogiidae
Distribution. Cosmopolitan in temperate and tropical waters of the Atlantic, Pacific, and Indian oceans; concentrations of stranding records occur along E USA, South Africa, and New Zealand and to a lesser degree on French and Spanish coasts; precise at-sea distribution is unknown.
Distribution. Occurs from the temperate waters of S Atlantic, Indian, and S Pacific oceans to the waters of Antarctica. A record from Burma (= Myanmar) is thought to represent a vagrant individual. in Ziphiidae
Distribution. Occurs from the temperate waters of S Atlantic, Indian, and S Pacific oceans to the waters of Antarctica. A record from Burma (= Myanmar) is thought to represent a vagrant individual.
Distribution. Throughout the warmest waters of the Indian and Pacific oceans, it has a cross-equatorial distribution occurring from as far N as the Arabian Sea, S India, Japan, and Mexico to as far S as South Africa and Australia; its occurrence appears to be relatively continuous within its distribution; it has not been recorded in the Atlantic Ocean. in Ziphiidae
Distribution. Throughout the warmest waters of the Indian and Pacific oceans, it has a cross-equatorial distribution occurring from as far N as the Arabian Sea, S India, Japan, and Mexico to as far S as South Africa and Australia; its occurrence appears to be relatively continuous within its distribution; it has not been recorded in the Atlantic Ocean.
Distribution. Endemic to cold temperate and subpolar waters of N Pacific Ocean, from the relatively shallow waters of the Bering Sea in the N to S Japan (W Pacific Ocean) and C California (E Pacific Ocean); itis the only species of Mesoplodon that commonly occurs in the Sea ofJapan. in Ziphiidae
Distribution. Endemic to cold temperate and subpolar waters of N Pacific Ocean, from the relatively shallow waters of the Bering Sea in the N to S Japan (W Pacific Ocean) and C California (E Pacific Ocean); itis the only species of Mesoplodon that commonly occurs in the Sea ofJapan.
Distribution. All warm temperate to tropical waters of the world and perhaps in cooler waters in the Southern Ocean and the N Pacific Ocean. It is the only species of beaked whales that commonly occurs in the Mediterranean Sea. in Ziphiidae
Distribution. All warm temperate to tropical waters of the world and perhaps in cooler waters in the Southern Ocean and the N Pacific Ocean. It is the only species of beaked whales that commonly occurs in the Mediterranean Sea.
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Dataset of Paper "Solar Water Disinfection in high-volume containers: Are naturally occurring substances attenuating factors of radiation?" (DOI: https://doi.org/10.1016/j.cej.2020.125852)
<p>Dataset of Paper "Solar Water Disinfection in high-volume containers: Are naturally occurring substances attenuating factors of radiation?"</p> <p><strong>- </strong>Data of the water transmission spectra depending of naturally occurring substances presented in the water.</p> <p><strong>- </strong>Data of the <em>E. coli </em>inactivation profiles during solar disinfection in high volume containers to study the effect of different naturally occurring substances in water.</p> <p>- Comparison of experimental and estimated first-order kinetic constants for <em>E. coli</em> photoinactivation of first-order kinetic models of radiation attenuating substances in low-volume and high-volume containers.</p>
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Subspecies and Distribution. H.a.aquaticusOgilby,1841—WAfricafromGuineaandSierraLeonetoGhana. H.a.bates:Lydekker,1906—Nigeria,Cameroon,andpresumablyneighboringcountries. H. a. cottoni Lydekker, 1906 — Republic of the Congo, DR Congo, and presumably Uganda. The Water Chevrotain reportedly has a disjunct distribution, occurring in coastal forests from West Africa and in the rainforests of Central Africa from Nigeria to DR Congo, marginally entering Uganda. It has been listed for the following countries in Central Africa: Angola (Cabinda), Cameroon, Central African Republic, DR Congo, Equatorial Guinea, Gabon, Nigeria, Republic of the Congo, and Uganda (Semliki Valley). A record from Angola's Lunda Norte Province, near the Cassai River,is the southernmost record of the species. The species' status in some countries remains unclear. It is apparently absent from the Republic of Benin and Togo (but the speciesis listed as probable in the Ot Basin in Togo); its supposed occurrence in Guinea Bissau and Senegal remains unsupported by evidence. The species was listed for Sierra Leone, although its presence had been called into question. Photographic evidence seems to clarify that the species occurs in Sierra Leone. In 1850, a specimen was recorded from Gambia, but the present status of the species is unclear. Local people report the species from the Boké Préfecture in NW Guinea, which might be the northernmost area from which the species has been recently reported. Extensive field and market surveys there and in the southern Guinea savanna belt did notfind evidence for the species' presence. in Tragulidae
Subspecies and Distribution. H.a.aquaticusOgilby,1841—WAfricafromGuineaandSierraLeonetoGhana. H.a.bates:Lydekker,1906—Nigeria,Cameroon,andpresumablyneighboringcountries. H. a. cottoni Lydekker, 1906 — Republic of the Congo, DR Congo, and presumably Uganda. The Water Chevrotain reportedly has a disjunct distribution, occurring in coastal forests from West Africa and in the rainforests of Central Africa from Nigeria to DR Congo, marginally entering Uganda. It has been listed for the following countries in Central Africa: Angola (Cabinda), Cameroon, Central African Republic, DR Congo, Equatorial Guinea, Gabon, Nigeria, Republic of the Congo, and Uganda (Semliki Valley). A record from Angola's Lunda Norte Province, near the Cassai River,is the southernmost record of the species. The species' status in some countries remains unclear. It is apparently absent from the Republic of Benin and Togo (but the speciesis listed as probable in the Ot Basin in Togo); its supposed occurrence in Guinea Bissau and Senegal remains unsupported by evidence. The species was listed for Sierra Leone, although its presence had been called into question. Photographic evidence seems to clarify that the species occurs in Sierra Leone. In 1850, a specimen was recorded from Gambia, but the present status of the species is unclear. Local people report the species from the Boké Préfecture in NW Guinea, which might be the northernmost area from which the species has been recently reported. Extensive field and market surveys there and in the southern Guinea savanna belt did notfind evidence for the species' presence.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.