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21 results for “secondary distribution”
Figure 3. Distribution of Q3 values-Secondary Structure Prediction of Protein using Resilient Back Propagation Learning Algorithm
<p>The estimated accuracy for the α- helices (QH), β- strands (QE), C-coil states (QC), and three<br> state together (Q3) for the system is shown in Figure 3.</p>
Particle number size distributions associated with secondary organics
<p>We provide the model data used to reproduce the figures in our manuscript titled "secondary organic aerosol formation regulates cloud condensation nuclei in the global remote troposphere". </p>
Secondary data_Cell density distributions histograms
<p>Dataset containing secondary data regarding cell density. This data was used for the generation of histograms of cell density related to the article: <strong>The distinctive chemotactic responses of three marine herbivore protists to DMSP and related compounds.</strong> Therefore, provides information about the spatial distribution of three cultured dinoflagellates (<em>Karlodinium armiger, Gyrodinium dominans</em> and<em> Oxyrrhis marina</em>) responding to three chemical cues diffusing from a microcapillary. </p> <p>Nomenclature:</p> <p>bin_edge_um: spatial postion (um2) / counts: cell/um2 (density9 / concentration: uM</p>
Secondary Distribution of HIV Self-tests: an Innovative Strategy for Promoting Partner Testing and Reducing HIV Risk
ClinicalTrials.gov study NCT03135067. IPD Sharing: NO. Countries: 1. Publications: 37.
Evaluation of Secondary Distribution of HIV Self-screening Tests by Women With HIV
ClinicalTrials.gov study NCT05074251. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003). in Muridae
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003).
Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996). in Muridae
Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996).
Global distribution of primary and secondary vegetation at 1km spatial resolution
<p>This dataset provides the global spatial distribution of primary and secondary vegetation at approx. 1km spatial resolution (0.01°). It combines Hilda+ landuse/cover data by Winkler et al. (2020) and the global dataset on human influence by Riggio et al. (2020).</p> <p>The data consists of three NetCDF files: </p> <ul> <li>Primary vegetation</li> <li>Primary vegetation minimal use</li> <li>Secondary vegetation</li> </ul> <p>Primary vegetation is assigned where forests, unmanaged grass-/ shrubland or land with sparse vegetation according to the HILDA+ dataset (classes 44, 55, 66) are under full agreement of low human influence according to the global dataset on human influence.</p> <p>The same HILDA+ classes (44, 55, 66) with full agreement to be under very low human influence according to Riggion et al. (2020) are defined as primary vegetation minimal use.</p> <p>Secondary vegetation consists of forests, unmanaged grass-/ shrubland or land with sparse vegetation according to the Hilda+ dataset (classes 44, 55, 66) that are not classified as primary vegetation.</p> <p> </p> <p>Sources:</p> <p>Winkler, K., Fuchs, R., Rounsevell, M. D. A., Herold, M. (2020): HILDA+ Global Land Use Change between 1960 and 2019. PANGAEA. <a href="https://doi.org/10.1594/PANGAEA.921846">https://doi.org/10.1594/PANGAEA.921846</a> </p> <div> <div> <div> <div> <div> <div> <p>Riggio, J. et al. (2020): Global human influence maps reveal clear opportunities in conserving Earth’s remaining intact terrestrial ecosystems. Dryad. <a href="https://doi.org/10.25338/B80G7Z">https://doi.org/10.25338/B80G7Z</a></p> </div> </div> </div> </div> </div> </div> <p> </p> <p>This seperation of primary and secondary vegetation has been used e.g. in the following studies:</p> <p>Schneider et al. (2024): Effects of profit-driven cropland expansion and conservation policies. Nature Sustainability. <a href="https://doi.org/10.1038/s41893-024-01410-x">https://doi.org/10.1038/s41893-024-01410-x</a></p> <p><span>Piipponen et al. (2024): Protein and energy from grazing or crops - does livestock have a chance? Preprint: </span><a href="https://doi.org/10.21203/rs.3.rs-3392089/v1"><span>https://doi.org/10.21203/rs.3.rs-3392089/v1</span></a></p>
IFS-COMPO data related to the surface evaluation of Secondary Inorganic Aerosol distribution and wet deposition terms
<p>These datasets are used for the GMD submission related to the evaluation of the impact of applying EQSAM4Clim in the IFS-COMPO model on Secondary Inorganic Partcile surafec distributions and the resulting wet deposition totals for selected global regions.</p>
FIGURE 8. Macrochaetae distribution, a — S in Two Seira Lubbock 1869 (Collembola, Arthropleona, Entomobryidae) new to science, with remarkable secondary sexual characters
FIGURE 8. Macrochaetae distribution, a — S. raptora sp. n.; b — S. mantis sp. n. Schematic representation according to Christiansen and Bellinger (1998, 2000) modified from Jacquemart, 1974.
FIGURE 3. Croton ceanothifolius. A. Habit. B. Staminate flowers. C. Pistillate flower with bifid styles. D. Leaf with impressed primary and secondary veins. E. Nearly mature capsules. C. celtidifolius. F in Croton (Euphorbiaceae) of the Brazilian state of Paraná: an annotated checklist, species distribution, and identification key
FIGURE 3. Croton ceanothifolius. A. Habit. B. Staminate flowers. C. Pistillate flower with bifid styles. D. Leaf with impressed primary and secondary veins. E. Nearly mature capsules. C. celtidifolius. F. Habit (plant in the center with some orange leaves). G. Amber-colored latex. H. Stipules. I. Detail of acropetiolar stipitate nectary glands. J. Inflorescence with lower bisexual cymules. K. Pistillate flower with tetrafid styles. Photos: A.P.N. Pereira.
Secondary Distribution of HIV Self-tests Through Antenatal Care Clinic Attendees and Index Clients
ClinicalTrials.gov study NCT03705611. IPD Sharing: YES. Countries: 1. Publications: 1.
Effect of Spectacle Distribution to Myopic Secondary School Students in Rural Communities of Liaoning Province on Communities Academic High School Enrolment
ClinicalTrials.gov study NCT06714994. IPD Sharing: NO. Countries: 1. Publications: 5.
Hematocrit to Hemoglobin Ratio and Red Blood Cell Distribution Width in Polycythemia Vera and Secondary Erythrocytosis.
ClinicalTrials.gov study NCT05993065. IPD Sharing: Not stated. Countries: 1. Publications: 6.
Abundance, distribution and substrate association of Hong Kong stag beetles (Coleoptera: Lucanidae) in secondary forests
Open the record for dataset details and reuse information.
Molecular distributions of diacids, oxoacids and -dicarbonyls in summer- and winter-time fine aerosols from Tianjin, North China: Emissions from combustion sources and aqueous phase secondary formation
<p>To understand the characteristics and sources of organic aerosols (OA) in North China, we studied diacids, oxoacids and <em>α</em>-dicarbonyls in summer- and winter-time fine aerosols (PM<sub>2.5</sub>) collected from Tianjin. Oxalic (C<sub>2</sub>) acid was found to be the most abundant diacid species, followed by succinic (C<sub>4</sub>), malonic (C<sub>3</sub>) and sebacic (C<sub>8</sub>) acids, respectively. Glyoxylic (wC<sub>2</sub>) was the most abundant oxoacids followed by pyruvic acid. Concentrations of total diacids, oxoacids and <em>α</em>-dicarbonyls in winter were 2~3 times higher than those in summer, but their mass fractions in PM<sub>2.5</sub> were exactly the opposite. On average, total diacids carbon accounted for 2.9% in total carbon and 3.3% in organic carbon (OC) in summer and 1.8% and 2.0%, respectively, in winter. Their contributions to water-soluble OC (WSOC) was almost the same in both seasons (5.5% and 5.3%, respectively). Molecular distributions, mass ratios of selected diacid (C<sub>3</sub>, C<sub>4</sub>, M, F C<sub>6</sub>, Ph and C<sub>9</sub>) species and the linear relations among the selected species (including åC<sub>2</sub>-C<sub>4</sub> and åC<sub>8</sub>-C<sub>12</sub>) and with inorganic markers (K<sup>+</sup> and SO<sub>4</sub><sup>2-</sup>) implied that the diacids and related compounds are mainly originated from coal combustion and biomass burning emissions and produced in the atmosphere by both <em>in-situ</em> photochemical reactions at local scale and aging during long-range transport in both summer and winter. This study revealed that diacids and related compounds and WSOC are increased with increasing SO<sub>4</sub><sup>2-</sup> and they are produced in aqueous phase, implying the need of reduction in oxidants (NO<em><sub>x</sub></em> and SO<sub>2</sub>) emissions to control the water-soluble OA loading over North China.</p>
Genome-wide distribution of AdpA, a global regulator for secondary metabolism and morphological differentiation in Streptomyces, revealed the extent and complexity of the AdpA regulatory network.
GEO Series GSE33994. Streptomyces griseus. 9 samples. Type: Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing.
Genome-wide distribution of AdpA, a global regulator for secondary metabolism and morphological differentiation in Streptomyces [liquid]
GEO Series GSE34036. Streptomyces griseus. 2 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
The Effect of Subcutaneous Immunoglobulin Gammanorm on the Distribution of IgG Subclasses and on Immunity of Patients With Secondary Immunodeficiency
ClinicalTrials.gov study NCT03369301. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Genome-wide distribution of AdpA, a global regulator for secondary metabolism and morphological differentiation in Streptomyces [solid]
GEO Series GSE34037. Streptomyces griseus. 3 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
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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.
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