Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
44
datasets available to search
ShareScore release 0.7.1
Dataset results
44 results for “organic agriculture”
The influence of inherent soil factors and agricultural management on soil organic matter
<p>The accumulation of soil organic matter (SOM) is vital to the agronomic and environmental functioning of agroecosystems, yet the relative influence of inherent soil properties and agricultural management practices on SOM dynamics are not often addressed in individual studies. Using a network of 218 operating farm fields across Wisconsin and southern Minnesota, USA, this research employs single variable analysis (ANOVA and regression) and regression tree analysis to assess the effects of soil properties (texture, drainage class, pH) and management variables related to crop rotation, tillage, cover cropping, and manure application on SOM, as well as total organic carbon (TOC) and total nitrogen (TN) in the upper 15 cm. Single variable analysis revealed that greater SOM, TOC, and TN were associated with poorly drained soil, tile-drained fields, high-clay content soil, and high biomass crop rotations. Soil organic matter (SOM) and TOC were strongly related (R<sup>2</sup>=0.71), but different regression trees were produced; SOM was most influenced by clay content, while TOC was most influenced by drainage class. Future assessment for the building of SOM or TOC should be conducted with drainage and texture class categories and on a regional basis, given that these factors influence the practices that occur within landscapes. A rapid building of data sets through unstructured sampling, including an abundance of meta-data, should be a research priority in agricultural science to identify practices to build SOM on a regional basis.</p>
The legacy of one hundred years of climate change for organic carbon stocks in global agricultural topsoils - full dataset
<p>This zip folder contains a txt and a shp file with predicted soil organic carbon stocks for a total of 931149 points on agricultural land across the globe at three different timepoints. The initial value (2018) for the scenarios c (constant carbon input) and v (variable carbon input) was derived from the FAO GSP Global SOC map published in 2018. the values in 1969 and 1919 are the results of backwards modelling with RothC model to estimate past climate change effects on SOC stocks. Details can be found in the publication " The legacy of one hundred years of climate change for organic carbon stocks in global agricultural topsoils" as published in Scientific Reports.</p>
Soil microbial diversity and community composition during conversion from conventional to organic agriculture
Open the record for dataset details and reuse information.
Data from: Leaching losses of dissolved organic carbon and nitrogen from agricultural soils in the upper US Midwest
Open the record for dataset details and reuse information.
Impact of soil inoculation on crop residue breakdown and carbon and nitrogen cycling in organically and conventionally managed agricultural soils
Open the record for dataset details and reuse information.
The influence of inherent soil factors and agricultural management on soil organic matter
Open the record for dataset details and reuse information.
Data from: Early impacts of cover crop selection on soil biological parameters during a transition to organic agriculture
Open the record for dataset details and reuse information.
Data from: Sensitivity to agricultural inputs and dispersal limitation determine the response of arable plants to time since transition to organic farming
Open the record for dataset details and reuse information.
Effects of land clearing for agriculture on soil organic carbon stocks in drylands: A meta-analysis
Open the record for dataset details and reuse information.
Organic farming benefits birds most in regions with more intensive agriculture
Open the record for dataset details and reuse information.
Reducing pesticides without organic certification? Potentials and limits of an intermediate form of agricultural production
Open the record for dataset details and reuse information.
Data from: A trait‒environment relationship approach to participatory plant breeding for organic agriculture
Open the record for dataset details and reuse information.
Raw data for "Plot-scale variability of organic carbon in temperate agricultural soils - Implications for soil monitoring"
<p>This dataset is the raw data that belongs to a peer-reviewed study on the small-distance variability of soil organic carbon in agricultural soils in Germany. It consists of three different files. The first file gives the coordinates of the 16 soil cores that were taken at each of the 16 sites (eight cropland and eight grassland sites). The second file gives the soil properties measured at each individual core (n=16 per site) and the third file the soil properties measured at each indivdual soil profile (n=6 per site).</p>
Steering microbiomes by organic amendments towards climate-smart agricultural soils
<p>We steered the soil microbiome via applications of organic residues (mix of cover crop residues, sewage sludge + compost, and digestate + compost) to enhance multiple ecosystem services in line with climate-smart agriculture. Our result highlights the potential to reduce greenhouse gases (GHG) emissions from agricultural soils by the application of specific organic amendments (especially digestate + compost). Unexpectedly, also the addition of mineral fertilizer in our mesocosms led to similar combined GHG emissions than one of the specific organic amendments. However, the application of organic amendments has the potential to increase soil C, which is not the case when using mineral fertilizer. While GHG emissions from cover crop residues were significantly higher compared to mineral fertilizer and the other organic amendments, crop growth was promoted. Furthermore, all organic amendments induced a shift in the diversity and abundances of key microbial groups. We show that organic amendments have the potential to not only lower GHG emissions by modifying the microbial community abundance and composition, but also favour crop growth-promoting microorganisms. This modulation of the microbial community by organic amendments bears the potential to turn soils into more climate-smart soils in comparison to the more conventional use of mineral fertilizers.</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).
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).
Steering microbiomes by organic amendments towards climate-smart agricultural soils
Open the record for dataset details and reuse information.
Dataset for: Short-term temperature history affects mineralization of fresh litter and extant soil organic matter, irrespective of agricultural management
<p>Dataset for the article:</p> <p>Mason-Jones, K., Vrehen, P, Koper, K., Wang, J., van der Putten, W.H., Veen, G.F. 2020. Short-term temperature history affects mineralization of fresh litter and extant soil organic matter, irrespective of agricultural management. Soil Biology and Biochemistry, 150, 107985.</p> <p>Article DOI: 10.1016/j.soilbio.2020.107985</p>
Data from: Inorganic fungicides as routinely applied in organic and conventional agriculture can increase palatability but reduce microbial decomposition of leaf litter
1. The application of fungicides is considered an indispensable measure to secure crop production. These substances, however, may unintentionally enter surface waters via runoff, potentially affecting the microbial community. To assess such risks adequately, authorities recently called for suitable test designs involving relevant aquatic microorganisms. 2. We assessed the structural and functional responses of leaf-associated microbial communities, which play a key role in the breakdown of allochthonous leaf material in streams, towards the inorganic fungicides copper (Cu) and elemental sulphur (S). These substances are of particular interest as they are authorized for both conventional and organic farming in many countries of the world. We used the food-choice of the amphipod shredder Gammarus fossarum (indicative for microorganism-mediated leaf palatability) as well as microbial leaf decomposition as functional endpoints. Moreover, the leaf-associated microbial communities were characterized by means of bacterial density, fungal biomass and community composition facilitating mechanistic understanding of the observed functional effects. 3. While Gammarus preferred Cu-exposed leaves over unexposed ones, microbial leaf decomposition was reduced by both Cu and S (up to 30%). Furthermore, Cu-exposure decreased bacterial densities (up to 60%), stimulated the growth of leaf-associated fungi (up to 100%) and altered fungal community composition, while S did not affect any of the assessed structural endpoints. 4. Synthesis and applications. We observed both structural and functional changes in leaf-associated microbial communities at inorganic fungicide concentrations realistic for surface water bodies influenced by conventional and organic farming. Our data hence justify a careful re-evaluation of the environmental safety of the agricultural use of these compounds. Moreover, inclusion of an experimental design similar to the one used in the present study in lower-tier environmental risk assessments of antimicrobial compounds may aid to safeguard the integrity of aquatic microbial communities and the functions they provide.
Data from: Inorganic fungicides as routinely applied in organic and conventional agriculture can increase palatability but reduce microbial decomposition of leaf litter
Open the record for dataset details and reuse information.
ScienceDex guides
Understand access before you commit
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.