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458 results for “Data Protection”

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dryad36/100

Data from: The protected flora of long-established cemeteries in Hungary: using historical maps in biodiversity conservation

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publicMay 2021View details →
dryad36/100

Data from: Marine protected areas rescue a sexually selected trait in European lobster

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publicMay 2020View details →
dryad36/100

Data from: Impact of agroecological protection practices against cucurbit infesting fruit flies (Diptera: Tephritidae) in Morogoro, Tanzania

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publicAug 2024View details →
dryad36/100

Data from: TNFAIP9 protects against the development of the early stage of chronic kidney disease: Focus on inflammation and fibrosis

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publicDec 2024View details →
dryad36/100

Data from: Ice vests extend physiological work time while wearing explosive ordnance disposal protective clothing in hot and humid conditions

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publicSep 2024View details →
dryad36/100

Data for: Does parasitoid species diversity promote protective symbiont diversity?

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publicMar 2024View details →
dryad36/100

Data from: Thermal plasticity in protective wing pigmentation is modulated by genotype and food availability in an insect model of seasonal polyphenism

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publicJun 2024View details →
dryad36/100

Data from: An approach to incorporating inferred connectivity of adult movement into marine protected area design with limited data

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publicMar 2019View details →
dryad36/100

Data from: Translocation with targeted vaccination is the most effective strategy to protect an island endemic bird threatened by West Nile virus

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publicMar 2021View details →
dryad36/100

Data for: Functions of coastal feeder bluff systems: Implications for prioritizing protection and restoration

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publicOct 2025View details →
dryad36/100

Data and code for: Carnivore exclosures to protect sheep affect the distribution of a wild cervid

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publicAug 2024View details →
dryad36/100

Data for: Protective functions of Biocrusts on the Great Wall of China

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publicNov 2023View details →
dryad36/100

Data from: A nanovaccine for immune activation and prophylactic protection of atherosclerosis in mouse models

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publicFeb 2025View details →
dryad36/100

Data for: Design and testing of a sew-free origami mask for improvised respiratory protection

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publicJul 2023View details →
zenodo32/100

Supplementary material 1 from: Biniari K, Daskalakis I, Bouza D, Stavrakaki M (2019) Comparative study of qualitative and quantitative characters of grape cultivar 'Mavrodafni' (Vitis vinifera L.) and 'Renio' grown in different regions of the Protected Designation of Origin Mavrodafni Patras. Viticulture Data Journal 1: e37852. https://doi.org/10.3897/vdj.1.e37852

<p>This is the raw dataset of the measurements performed on the samples collected from the two varieties from the different locations. There are three repetitions per measurement and no statistical analysis has been performed.</p>

opencc-zeroJan 2020View details →
dryad32/100

Data from: Assessing the effectiveness of a national protected area network in maintaining carnivore populations

<p>Protected areas (PAs) are essential to prevent further biodiversity loss yet their effectiveness varies largely with governance and external threats. Although methodological advances have permitted assessments of PA effectiveness in mitigating deforestation, we still lack similar studies for the impact of PAs on wildlife populations. Here we demonstrate the application ofuse an innovative combination of matching methods and hurdle-mixed models with a large-scale and long-term dataset of unprecedented coverage for Finland's large carnivore species. We show that the national PA network , at the national level, PAs does not support higher densities than non-protected habitat for 3 of the 4 species investigated. For the brown bear, PAs appear to have lower densities than non-protected areas. For some species, PA effects interact with region or time, i.e. wolverine densities decreased inside PAs over the study period and lynx densities increased inside eastern PAs. Although we show that matching approaches could and should be applied to wildlife population data, Wwe support their application of matching methods in combination of additional analytical frameworks for deeper understanding of conservation impacts on wildlife populations. These methodological advances are crucial for improving PA targets and extremely timely for preparing ambitious PA targets a post-2020 global framework for biodiversity.</p>

opencc-zeroApr 2020View details →
dryad32/100

Data from: Upgrades of coastal protection infrastructure affect benthic communities

<ol> <li>Sea level rise, storm surges, aging and wear are forcing upgrades to breakwaters and seawalls to protect coastal areas from erosion and inundation. Such upgrades involve the introduction of new material which may consequently act as an ecological disturbance that can alter established marine communities and ecosystem function. Mitigating ecological impacts requires an understanding of how species assemblages are affected by such works.</li> <li>Here, we use the major upgrade of a regularly wave-overtopped breakwater as a case study to evaluate the impacts of upgrades to hard coastal protection structure on benthic rocky reef communities. An asymmetrical Before-After Control-Impact (BACI) experimental design was used to test interactive effects of the infrastructure upgrades on benthic communities.</li> <li>While benthic assemblages were not significantly different from controls prior to the upgrade, improving the defensive capacity of the breakwater significantly changed community structure. Notably, most taxonomic groups showed higher cover at the control sites than at the impacted site post-upgrade, with articulated calcareous algae (e.g. <i>Corallina officinalis</i> and <i>Amphiroa anceps</i>) showing an opposite trend.</li> <li> <i>Synthesis and applications</i>: Ecological implications and structural limitations make regular upgrading of existing infrastructure unsuitable as a long-term management strategy. More sustainable alternatives need to be considered, such as decommissioning of structures and retreat from flood-prone areas. This transition, however, will take time and requires a change of mindset and policies. Where upgrades are urgent, eco-engineering techniques can mitigate impacts to habitats and associated taxa.</li> </ol>

opencc-zeroAug 2020View details →
dryad32/100

Achieving Bio-Protection in New Zealand Ecosystems mesocosm data

<p>We established 160 experimental ecosystems (mesocosms), manipulated interactions between plants, soil biota and invertebrate herbivores in a fully factorial design. Each mesocosm was grown in a 125 L pot (575 mm diameter, Fig. 1B), and comprised one of 20 unique, eight-species plant communities varying orthogonally in the proportion of exotic and woody shrub/tree species (0-100% and 0-63%, respectively). These plants were taken from a pool of 20 exotic and 19 native/endemic New Zealand plant species. Soil biota were manipulated using a modified plant-soil feedback approach, where each plant species was grown in monoculture in 10 L pots containing field-collected soil for 9-10 months, allowing the conditioning of typical associated soil biota for each of the plant species. We created 'home' soils by taking the conditioned soil from each of the eight representative species in a mesocosm and mixing it together to create a single inoculum. Each 'home' soil mixture was also used as an 'away soil' in a different mesocosm that did not contain any of the representative plants in that inoculum. These soils were intended to increase the relative biomass in inocula of specialized and preferred interaction partners of the resident (or non-resident) plant species. Invertebrate insect herbivore populations were added into half of the mesocosms with home soils and half with away soils. Thirteen invertebrate herbivore species introduced into the mesocosms successfully established, along with seven self-colonizing species, totaling 20 species in all. All mesocosms were sealed with mesh cages (15% shade factor) designed to retain added herbivores and exclude others from entering. In each mesocosm, we measured distinct ecosystem properties and processes that are relevant to carbon cycling dynamics: above and belowground biomass; total <i>in situ</i> soil respiration; basal respiration; microbial biomass (measured as substrate-induced respiration); decomposition (rate of standardized substrate mass loss); soil organic matter; nitrogen availability; herbivore biomass; arbuscular mycorrhizal and other fungal biomass (using neutral- and phospho-lipid fatty acid [NLFA and PLFA] biomarkers, respectively); and bacterial biomass (PLFA).</p>

opencc-zeroAug 2020View details →
dryad32/100

Data from: Modelling the current and future biodiversity distribution in the Chilean Mediterranean Hotspot. The role of protected areas network in a warmer future

Aim: Mediterranean Chile is part of the five recognized Mediterranean-type climates in the world and harbors a very rich floral diversity. Climate change has been reported as a significant threat to its biodiversity. We used the flora of Mediterranean Chile to analyze how biodiversity patterns, as measured by Phylogenetic Diversity, genus and species richness will respond to climate change scenarios and identify the areas that will harbor the greatest evolutionary potential and biodiversity richness. We also evaluated how these spatial patterns are depicted within the current network of protected areas. Location: Chilean Mediterranean climate-type Region, South America. Methods: Biodiversity metrics were evaluated for current and future climatic scenarios. Species distribution models were done using Maxent for 1.727 species and 571 genera. Relationships between species/genera gain, loss and turnover were evaluated. For Mediterranean endemic species, loss and gain was also related to life form. Finally, variation in species gain, loss and turnover was evaluated in future climate change scenarios within and outside Mediterranean Chile state protected areas. Results: We found a general decrease in species richness in the entire Region toward future climate change scenarios. Phylogenetic Diversity is predicted to be higher than expected by richness in the north and south of the area, and lower than expected by richness in the Andes mountain. The highest average species and genus loss is predicted to occur outside the protected areas, meanwhile species and genus gain is higher within them. Main conclusions: Future biodiversity patterns are reported here for the first time in the Chilean Mediterranean Region. Our findings enhance the importance of the current protected areas to harbor this future variation, despite their reduced number and size along the region.

opencc-zeroAug 2020View details →
dryad32/100

Data from: Assessing the effectiveness of protected areas for conserving range-restricted rainforest butterflies in Sabah, Borneo

Rainforests on Borneo support exceptional concentrations of endemic insect biodiversity, but many of these forest-dependent species are threatened by land-use change. Totally protected areas (TPAs) of forest are key for conserving biodiversity, and we examined the effectiveness of the current TPA network for conserving range-restricted butterflies in Sabah (Malaysian Borneo). We found that mean diurnal temperature range and precipitation of the wettest quarter of the year were the most important predictors of butterfly distributions (N = 77 range-restricted species), and that species richness increased with elevation and aboveground forest carbon. On average across all species, TPAs were effective at conserving ~43% of species' ranges, but encompassed only ~40% of areas with high species richness (i.e. containing at least 50% of our study species). The TPA network also included only 33-40% of areas identified as high priority for conserving range-restricted species, as determined by a systematic conservation prioritization analysis. Hence, the current TPA network is reasonably effective at conserving range-restricted butterflies, although considerable areas of high species richness (6565 km2) and high conservation priority (11,152-12,531 km2) are not currently protected. Sabah's remaining forests, and the range-restricted species they support, are under continued threat from agricultural expansion and urban development, and our study highlights important areas of rainforest that require enhanced protection.

opencc-zeroSep 2020View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record