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ShareScore release 0.9.0
Dataset results
13 results for “artificial production”
Effects of intercropping on the herbage production of a binary grass-legume mixture (Hedisarum coronarium L. and Lolium multiflorum Lam.) under artificial shade in Mediterranean rainfed conditions
<p>This dataset refers to the experimental raw data (csv version) collected within the trial reported in the concerned article on the following parameters:</p> <p>1. crop aboveground biomass, splitted per field, mowing, crop, treatment and replicate (crop aboveground biomass.csv)</p> <p>2. cumulated crop aboveground biomass, splitted per field, year, crop, treatment and replicate (cumulated crop aboveground biomass_year.csv)</p> <p>3. cumulated crop aboveground biomass for the two years of the growing cycle, splitted per field, crop, treatment and replicate (cumulated crop aboveground biomass_2years.csv)</p> <p>4. partial and total RYT splitted per year, field and treatment (RYT_year)</p> <p>5. partial and total RYT for the two years of the growing cycle, splitted per field and treatment (RYT_2years)</p> <p> </p> <p><br> </p>
Seagrass production around artificial reefs is resistant to human stressors
<p>Primary production underpins most ecosystem services, including carbon sequestration and fisheries. Artificial reefs (ARs) are widely used for fisheries management. Research has shown that a mechanism by which AR in seagrass beds can support fisheries and carbon sequestration is through increasing primary production via fertilization from aggregating fish excretion. Seagrass beds are heavily affected by anthropogenic nutrient input and fishing that reduces nutrient input by consumers. The effect of these stressors is difficult to predict because impacts of simultaneous stressors are typically non-additive. We used a long-term experiment to identify the mechanisms by which simultaneous impacts of sewage enrichment and fishing alter seagrass production around ARs across non-orthogonal gradients in human-dominated and relatively unimpacted regions in Haiti and The Bahamas. Merging trait-based measures of seagrass and seagrass ecosystem processes, we found that ARs consistently enhanced per capita seagrass production and maintained ecosystem-scale production despite drastic shifts in controls on production from human stressors. Importantly, we also show that coupled human stressors on seagrass production around ARs were additive, contrasting expectations. These findings are encouraging for conservation because they indicate that seagrass ecosystems are highly resistant to coupled human stressors and that ARs promote ecosystem services even in human-dominated ecosystems.</p>
Data from: Artificial nighttime lighting and herbivory interactively reduce the biomass production of invasive plants while enhancing that of native plants
Open the record for dataset details and reuse information.
Seagrass production around artificial reefs is resistant to human stressors
Open the record for dataset details and reuse information.
Portfolio simplification arising from a century of change in salmon population diversity and artificial production
<p>1. Population and life-history diversity can buffer species from environmental variability and contribute to long-term stability through differing responses to varying conditions akin to the stabilizing effect of asset diversity on financial portfolios. While it is well known that many salmon populations have declined in abundance over the last century, we understand less about how different dimensions of diversity may have shifted. Specifically, how has diminished wild abundance and increased artificial production (i.e., enhancement) changed portfolios of salmon populations, and how might such change influence fisheries and ecosystems?</p> <p>2. We apply modern genetic tools to century-old sockeye salmon (<em>Oncorhynchus nerka</em>) scales from Canada's Skeena River watershed to (<em>i</em>) reconstruct historical abundance and age-trait data for 1913–1947 to compare with recent information, (<em>ii</em>) quantify changes in population and life-history diversity and the role of enhancement in population dynamics, and (<em>iii</em>) quantify the risk to fisheries and local ecosystems resulting from observed changes in diversity and enhancement.</p> <p>3. The total number of wild sockeye returning to the Skeena River during the modern era is 69% lower than during the historical era; all wild populations have declined, several by more than 90%. However, enhancement of a single population has offset declines in wild populations such that aggregate abundances now are similar to historical levels.</p> <p>4. Population diversity has declined by 70%, and life-history diversity has shifted: populations are migrating from freshwater at an earlier age, and spending more time in the ocean. There also has been a contraction in abundance throughout the watershed, which likely has decreased the spatial extent of salmon provisions to Indigenous fisheries and local ecosystems. Despite the erosion of portfolio strength that this salmon complex hosted a century ago, total returns now are no more variable than they were historically perhaps in part due to the stabilizing effect of artificial production.</p> <p>5.<em> Policy implications</em>. Our study provides a rare example of the extent of erosion of within-species biodiversity over the last century of human influence. Rebuilding a diversity of abundant wild populations – that is, maintaining functioning portfolios - may help ensure that watershed complexes like the Skeena are robust to global change. </p>
Portfolio simplification arising from a century of change in salmon population diversity and artificial production
Open the record for dataset details and reuse information.
Software product line problem in DIMACS format (artificial augments)
<p>Some artificial augment for the software product line problem in dimacs format.</p>
Artificial Melanogenesis by Confining Melanin/Polydopamine Production Inside Polymersomes
<p>Data underlying the figures in the publication “Artificial melanogenesis by confining melanin/polydopamine production inside polymersomes”, published in <em>Macromolecular Bioscience, </em><strong>2021</strong>.</p> <p>Table of contents:</p> <p><strong>1. Figure 1</strong>; Zip. archive containing the experimental data for <em>Figure 1</em>. TEM micrographs and corresponding DLS and SLS revealing the morphology and size of (A) Melanin-polymersomes (with Tyrosinase), (B) PDA-polymersomes (with Tyrosinase), (C) empty polymersomes rehydrated with PBS only, and (D) Tyrosinase-polymersomes.</p> <p><strong>2. Figure 2</strong>; Zip. archive containing the experimental data for <em>Figure 2</em>. (A) Zeta potential values showing the absence of Dopamine, L-DOPA or Tyrosinase adsorption at the surface of polymersomes. TEM micrographs of polymersome clusters formed after adding (B) L-DOPA with Tyrosinase, (C) Dopamine with Tyrosinase, (D) L-DOPA and (E) Dopamine to empty polymersomes.</p> <p><strong>3. Figure 3</strong>; Zip. archive containing the experimental data of the graphs in <em>Figure 3</em>. Melanin and PDA formation within polymersomes monitored via UV-vis spectroscopy. Absorption spectra measured at t = 0 (grey), t=12 h (cyan) and t=24 h (orange) of incubation at 37 °C of (A) Empty polymersomes, (B) Tyrosinase polymersomes, (C) L-DOPA polymersomes, (D) L-DOPA polymersomes (with Tyrosinase), (E) Dopamine polymersomes, (F) Dopamine polymersomes (with Tyrosinase).</p> <p><strong>4. Figure 4</strong>; Zip. archive containing the experimental data for <em>Figure 4</em>. Interaction of polymersome-based melanosome mimics with HaCaT cells. (A) Cell proliferation assay showing the non-toxicity of different polymersomes encapsulating dopamine and Tyrosinase (dashed purple), L-DOPA and Tyrosinase (dashed grey), dopamine (purple), L-DOPA (grey), PBS (yellow), Tyrosinase (dashed yellow) compared to control PBS without polymersomes (blue). Cells were incubated with respective polymersomes for 24 h. (B) Cell proliferation assay showing the cytotoxicity of free L-DOPA/dopamine (with and without Tyrosinase) compared to PBS. (C) Cell proliferation assay showing the cytotoxicity/cell protection effect of different kinds of polymersomes after 40 min of UV-irradiation of cells treated for 24 h with polymersomes. (D) CLSM images showing perinuclear localization of model polymersomes (encapsulating fluorescent Atto-488) in keratinocytes. Statistical significance was shown as p values < 0.02.</p> <p> </p>
Product Preference With Systane Compared to Artificial Tears on Frequency of Drop Use
ClinicalTrials.gov study NCT00347984. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Comparison of Two Artificial Intelligence Scribe Products on Pediatric Subspecialty Provider Wellness and Experience, Patient Satisfaction, and Efficiency.
ClinicalTrials.gov study NCT07157943. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Functional Electrical Stimulation for Production of Artificial Cough
ClinicalTrials.gov study NCT00589199. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Production of artificial piRNAs in flies and mice
GEO Series GSE32435. Drosophila melanogaster; Mus musculus. 11 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Analysis of New Materials and Artificial Turf Products: Influence and Impact on Athlete Performance and Perception
ClinicalTrials.gov study NCT06939218. IPD Sharing: Not stated. Countries: 0. Publications: 0.
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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.
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.