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242 results for “distributed systems”
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.
Distribution. Cape York Peninsula of NE Queensland, N of the Stewart River and the Coen-Archer River system, including Mcllwraith and Iron ranges. in Phalangeridae
Distribution. Cape York Peninsula of NE Queensland, N of the Stewart River and the Coen-Archer River system, including Mcllwraith and Iron ranges.
Distribution. France (W & S of Loire River) and N & NE Iberian Peninsula (E Cantabrian coast and Mts, N Iberian System Mts, N Ebro Basin, Pyrenees, and N Catalonia). in Talpidae
Distribution. France (W & S of Loire River) and N & NE Iberian Peninsula (E Cantabrian coast and Mts, N Iberian System Mts, N Ebro Basin, Pyrenees, and N Catalonia).
Distribution. SE Madagascar, currently known from S of the Mangoro/Nesivolo river systems in the forests of Manara, Vatoalatsaka, Sangalampona, Mahasoarivo, and Ranomatana; the S extent of the distribution remains unclear. The precise distributional limits of Peyrieras's Woolly Lemur and in particular its relationship to the Southern Woolly Lemur (A. meridionalis) and the Manombo Woolly Lemur (A. ramanantsoavanai) in the S are undetermined. in Indriidae
Distribution. SE Madagascar, currently known from S of the Mangoro/Nesivolo river systems in the forests of Manara, Vatoalatsaka, Sangalampona, Mahasoarivo, and Ranomatana; the S extent of the distribution remains unclear. The precise distributional limits of Peyrieras's Woolly Lemur and in particular its relationship to the Southern Woolly Lemur (A. meridionalis) and the Manombo Woolly Lemur (A. ramanantsoavanai) in the S are undetermined.
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. Sierra Leone (W limit Rokupr, 9° N, 12° 34' 48" W), S Guinea, Liberia, and W Ivory Coast (E to the Nzi-Bandama River system). in Cercopithecidae
Distribution. Sierra Leone (W limit Rokupr, 9° N, 12° 34' 48" W), S Guinea, Liberia, and W Ivory Coast (E to the Nzi-Bandama River system).
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.
Distribution. NW DR Congo and NE Republic of the Congo, in lowland forests of the Congo Basin on both sides of the lower and middle Congo (c.16" E to 26°-27° E); S of the Congo Riverits distribution extends E to the Lomami River system (c.3° N to 6° 30° S); it has also been recorded on twoislands in the Sangha River. Its presence in NE Angola requires confirmation. in Cercopithecidae
Distribution. NW DR Congo and NE Republic of the Congo, in lowland forests of the Congo Basin on both sides of the lower and middle Congo (c.16" E to 26°-27° E); S of the Congo Riverits distribution extends E to the Lomami River system (c.3° N to 6° 30° S); it has also been recorded on twoislands in the Sangha River. Its presence in NE Angola requires confirmation.
Subspecies and Distribution. C.p.petauristaSchreber,1774—C&EIvoryCoast(EoftheSassandraRiver),Ghana,andWTogo;possiblyinBenin. C. p. buettikofer: Jentink, 1886 — SE Senegal, S Guinea-Bissau, S Guinea, Sierra Leone, Liberia, and W Ivory Coast (W of the Nzo-Sassandra River system). in Cercopithecidae
Subspecies and Distribution. C.p.petauristaSchreber,1774—C&EIvoryCoast(EoftheSassandraRiver),Ghana,andWTogo;possiblyinBenin. C. p. buettikofer: Jentink, 1886 — SE Senegal, S Guinea-Bissau, S Guinea, Sierra Leone, Liberia, and W Ivory Coast (W of the Nzo-Sassandra River system).
Distribution. Endemic to DR Congo, in the C Congo Basin S & W of the Congo-Lualaba River System. in Cercopithecidae
Distribution. Endemic to DR Congo, in the C Congo Basin S & W of the Congo-Lualaba River System.
Other common names: East African Grammomys, Rwenzori Grammomys, Rwenzori Thicket Rat Taxonomy. Thamnomys ibeanus Osgood, 1910, Molo, Kenya. Grammomys ibeanus was previously includ-ed in G. cometes, but molecular data show it to be closer to G. macmillani. Monotypic. Distribution. Occurs quite widely in E Africa associated with mountains of the Rift Valley system and the Eastern Arc, including S South Sudan, E Uganda, Kenya, Tanzania, Malawi, and Mozambique. in Muridae
Other common names: East African Grammomys, Rwenzori Grammomys, Rwenzori Thicket Rat Taxonomy. Thamnomys ibeanus Osgood, 1910, Molo, Kenya. Grammomys ibeanus was previously includ-ed in G. cometes, but molecular data show it to be closer to G. macmillani. Monotypic. Distribution. Occurs quite widely in E Africa associated with mountains of the Rift Valley system and the Eastern Arc, including S South Sudan, E Uganda, Kenya, Tanzania, Malawi, and Mozambique.
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).
Supplementary material 3 from: Saltmarsh DM, Bowser ML, Morton JM, Sirley Lang S, Shain D, Dial R (2016) Distribution and abundance of exotic earthworms within a boreal forest system in southcentral Alaska. NeoBiota 28: 67-86. https://doi.org/10.3897/neobiota.28.5503
Analysis dataset : Explanation note: This spreadsheet file contains all original measurements and derived metrics used in the analyses. It is arranged in a relational format. The sheet labeled site_data contains all site-level data, including original data and some derived metrics; the plot_data sheet contains plot-level data. The earthworm_lengths sheet contains all of the earthworm length measurements and, by implication, the occurrence data. The two response_data sheets hold data derived from the first three sheets that were used in subsequent analyses.
Supplementary material 2 from: Saltmarsh DM, Bowser ML, Morton JM, Sirley Lang S, Shain D, Dial R (2016) Distribution and abundance of exotic earthworms within a boreal forest system in southcentral Alaska. NeoBiota 28: 67-86. https://doi.org/10.3897/neobiota.28.5503
Specimen records : Explanation note: Occurrence data are provided for earthworm specimens collected. Data field definitions are those used by Arctos (http://arctos.database.museum/, http://arctosdb.org/).
Supplementary material 1 from: Saltmarsh DM, Bowser ML, Morton JM, Sirley Lang S, Shain D, Dial R (2016) Distribution and abundance of exotic earthworms within a boreal forest system in southcentral Alaska. NeoBiota 28: 67-86. https://doi.org/10.3897/neobiota.28.5503
Alaska earthworm records : Explanation note: Earthworm records from Alaska exclusive of data from the present study are compiled. All literature items cited are included in the References section of the manuscript.
Networks files of main scenarios analysed in "Distributed photovoltaics provides key benefits for a highly renewable European energy system"
<p>This repository contains the network files (.nc) of the main scenarios (A, B, C, and D) used for analysis in the paper. The code for reproducing these files plus other network files used for sensitivity analysis plus the Jupyter notebooks used for creating all the figures in the paper are available at: https://github.com/Parisra/Distributed-PV-paper </p>
Importance of Parametric Uncertainty in Predicting Probability Distributions for Burst Wait-Times in Fissile Systems
<p>In accordance with EPSRC funding requirements this folder contains all raw data relevant to the named paper: Importance of Parametric Uncertainty in Predicting Probability Distributions for Burst Wait-Times in Fissile Systems.</p>
Inventory of scientific publications on Distributed Hydrogen Systems from 2000-2023
<p>This Excel sheet contains a comprehensive list of scientific publications on distributed hydrogen systems from the years 2000 to 2023. Each entry includes the following details:</p> <ul> <li><strong>Title</strong>: The title of the publication.</li> <li><strong>Authors</strong>: The names of the authors who contributed to the publication.</li> <li><strong>Year</strong>: The year the publication was released.</li> <li><strong>DOI</strong>: The Digital Object Identifier, providing a unique and permanent link to the publication.</li> <li><strong>Journal Name</strong>: The name of the journal where the publication appeared.</li> <li><strong>Impact Factor</strong>: The impact factor of the journal, indicating its influence and relevance in the scientific community.</li> </ul>
Fig. 7 in Diversity and Distribution of Peritrich Ciliates on the Snail Physa acuta Draparnaud, 1805 (Gastropoda: Physidae) in a Eutrophic Lotic System
Fig. 7. Non-metric multidimensional scaling (NMDS) for peritrichs species abundance on Physa acuta shell. Stress = 0. C_pol = Carchesium polypinum, E_plic = Epistylis plicatilis, E_sp = Epistylis sp., O_art = Opercularia articulata, T_kel = Thuricola kellicottiana, V_cam = Vorticella campanula, V_sp = Vorticella sp.
Fig. 6 in Diversity and Distribution of Peritrich Ciliates on the Snail Physa acuta Draparnaud, 1805 (Gastropoda: Physidae) in a Eutrophic Lotic System
Fig. 6. Abundance, density, diversity and dominance of peritrich epibionts on sites of the Physa acuta shell. Different letters indicate statistical differences p <0.05 and the symbol *indicate p> 0.05.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.