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128 results for “Yearly activity”
Copernicus EMS flood activations delimitations (2012 - 2020) rasterised at 30m and aggregated per year and season
<p>This dataset was created as part of the <a href="https://opendatascience.eu/">Geo-harmonizer project</a>, with the scope of making open data easier to access. It contains all the flood activations mapped by the <a href="https://emergency.copernicus.eu/mapping/list-of-activations-rapid">Copernicus Emergency Rapid Mapping Service</a> between 2012 and 2020. To obtain these GeoTIFFs, the vector data packages from CEMS were individual downloaded, rasterized and mosaicked per year and season, resampled at 30-m and reprojected to <a href="https://epsg.io/3035">EPSG 3035: ETRS89-extended / LAEA Europe</a>. If no CEMS flood activation was identified in a specific year and season, the raster was not created. The rasters are provided as COG files, type=16Int, the flooded area pixels have value 100, nodata value is 255.</p> <p>To allow an easier and faster search through all 2012 - 2020 CEMS flood activations, we have prepared a point vector layer (geojson) containing one point for each flood activation area of interest with the following attributes attached: CEMS identification number <ems_id>, area of interest defined by CEMS <ems_aoi>, URL link to the CEMS activation <ems_link>, year of the event <year_start>, <year_end> , <season> and the name of the <geo_harmonizer_raster> where the 30m rasterised delimitations of the flooded areas of the corresponding flood activation can be found. </p> <p>For any additional questions regarding the data, please contact the author at codrina.ilie[at]terrasigna.com.</p> <p>The Copernicus Emergency Rapid Mapping Service data access policy is available <a href="https://emergency.copernicus.eu/mapping/sites/default/files/files/CopernicusEMS-Data_and_Dissemination_Policy.pdf">here</a>.</p>
Dataset in the article "Sedimentary record off the Yangtze River estuary and its response to typhoons and human activities over the past 70 years"
<p>The original data presented here is related to the article “Sedimentary record off the Yangtze River estuary and its response to typhoons and human activities over the past 70 years”</p>
The datasets for the paper "Spatial and temporal distribution of lobate scarps in the lunar south polar region: Evidence for latitudinal variation of scarp geometry, kinematics and formation ages, continuous tectonic activity in the last 100 million years and seismically safe south pole Artemis human landing site" Geophysical Research Letters.
<p>This dataset provides the original data that were used for preparing the illustrations, figures and tables.</p>
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).
DiverReef: The global repository of divers' and snorkelers' behavior during tourism activities and their interactions with reef environments over 20 years
<p>The DiverReef database provides the first public dataset on the underwater behavior of recreational divers and snorkellers in shallow reef environments (< 25 m depth) globally and their interactions with the reef seascape and/or reef benthic sessile organisms. The dataset comprises 19 years of data (2004-2023) by observing the behavior of 2312 recreational divers and snorkelers in 9 countries at 19 diving destinations and 176 diving sites. The data were collected through on-site observation of divers' behavior during tourism activities and their physical interactions with the reef structure and/or benthic reef sessile organisms. Observers discretely followed divers and recorded their behavior and interactions with the reef over set time periods. Interactions were described as "contact" and "damage", the latter refers to when physical damage to a benthic organism or the reef structure was observed. Besides behavior, observers also recorded data on the type of diving activity (scuba or snorkeling), profiles of the divers (gender and experience), use of cameras by the divers, visibility, type of reef formation and marine protection status of the dive site. This is the external repository where the DiverReef database is archived. This database has an attribution-share alike (CC BY-SA 4.0 Deed) copyright restriction. When using this database, the original paper in the Ecology journal (include DOI when available) must be cited.</p>
Figure 2. Mean monthly temperatures per year for the period April 1998 in Effect of temperature on the flight activity of culicids in Buenos Aires City, Argentina
Figure 2. Mean monthly temperatures per year for the period April 1998 to March 2001, and minimum, maximum and mean temperatures for the period 1861–2003. Buenos Aires City.
Unaltered soil microbial community composition, but decreased metabolic activity in a semi-arid grassland after two years of passive experimental warming
<p>Soil microbial communities regulate soil carbon feedbacks to climate warming through microbial respiration (i.e. metabolic rate). A thorough understanding of the responses of composition, biomass and metabolic rate of soil microbial community to warming is crucial to predict soil carbon stocks in a future warmer climate. Therefore, we conducted a field manipulative experiment in a semi-arid grassland on the Loess Plateau of China to evaluate the responses of the soil microbial community to increased temperature from April 2015 to December 2017. Soil temperature was 2.0 <sup>o</sup>C higher relative to the ambient when open-top chambers (OTCs) were used. Warming did not affect microbial biomass or the composition of microbial functional groups. However, warming significantly decreased microbial respiration, directly resulting from soil pH decrease driven by the co-mediation of aboveground biomass increase, inorganic nitrogen increase and moisture decrease. These findings highlight that the soil microbial community structure of semi-arid grasslands resisted the short-term warming by 2 <sup>o</sup>C, although its metabolic rate declined.</p>
Initial status and change in cognitive function mediate the association between academic education and physical activity in adults over 50 years of age
<p>The scripts for data management (i.e., from raw data to data used in the analyses) and for the models tested in the paper titled "Initial status and change in cognitive function mediate the association between academic education and physical activity in adults over 50 years of age".</p> <p>“SHARE_Data_merge_w8.R” --> merges the data between the 8 waves of measurement.</p> <p>“SHARE_computingVars_w8.R” --> computes the variables used in the abovementionned study.</p> <p>“Growth_curve_models.R” --> contains the statistical models tested in the abovementionned study.</p>
Supplemental from: Seasonal Variation in Thermal Biology and Water Balance in a Year-Round Active Neotropical Treefrog, Scinax fuscovarius
<p>This supplemental material is associated to the published article entitled: "Seasonal Variation in Thermal Biology and Water Balance in a Year-Round Active Neotropical Treefrog, Scinax fuscovarius" </p>
Association Between Sarcopenia and Urinary Incontinence And Effect Of Physical Activity Among Over 50 Years Old Adults
ClinicalTrials.gov study NCT05313360. IPD Sharing: NO. Countries: 1. Publications: 1.
Smart Walk 50+: Feasibility of a Smartphone-delivered Physical Activity Program for African American Women 50 Years and Older
ClinicalTrials.gov study NCT04073355. IPD Sharing: NO. Countries: 1. Publications: 1.
Trial Comparing Near Versus Distance Activities While Patching for Amblyopia in Children 3 to <7 Years Old
ClinicalTrials.gov study NCT00315198. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Vascular Effects of Achieving Minimal Disease Activity in Psoriatic Arthritis - a 2 Year Prospective Cohort Study
ClinicalTrials.gov study NCT02232321. IPD Sharing: Not stated. Countries: 1. Publications: 2.
The Effects of Traditional Massage on Spasticity and Activity of Children(2 to 10 Years) With Cerebral Palsy
ClinicalTrials.gov study NCT03771599. IPD Sharing: Not stated. Countries: 1. Publications: 9.
Levels of Daily Physical Activity and Sedentary Behaviour in Maastricht University's Undergraduate First Year Students
ClinicalTrials.gov study NCT03513341. IPD Sharing: YES. Countries: 1. Publications: 4.
Physical Activity and Dietary Behaviors of Adults 18 to 80 Years of Age
ClinicalTrials.gov study NCT00641849. IPD Sharing: NO. Countries: 1. Publications: 29.
After-school Game-Based Physical Activity Program Improves Physical Fitness of 9-10-Year-Old Children
ClinicalTrials.gov study NCT06919146. IPD Sharing: YES. Countries: 1. Publications: 1.
A Mobile Phone App to Promote Healthy Diet and Physical Activity in 2.5-year-olds
ClinicalTrials.gov study NCT04147039. IPD Sharing: NO. Countries: 1. Publications: 2.
Feasibility Trial of a Personalised Nutrition and Activity Programme for People With Lung Cancer Over 65 Years
ClinicalTrials.gov study NCT05404022. IPD Sharing: NO. Countries: 1. Publications: 2.
An Individualized Physical Activity Program in Patients Over 65 Years With Hematologic Malignancies
ClinicalTrials.gov study NCT04052126. IPD Sharing: NO. Countries: 1. Publications: 1.
ScienceDex guides
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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.