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4,775 results for “carbon”
NEON distributed initial soil characterization dataset (DP1.10047.001) modified for statistical analysis of organic carbon and extractable metals in Hall and Thompson (2021)
We compiled National Ecological Observatory Network (NEON) datasets related to the initial distributed soil sampling effort and subsetted them (removed samples with missing values for certain variables, and several samples with extreme values) for use in statistical analyses to describe relationships between soil organic carbon (SOC) and metals measured in several soil chemical extractions. The NEON provisional data products we used were DP1.10047.001 and DP1.10008.001, which were subsequently combined by NEON as a single data product DP1.10047.001, “Soil physical and chemical properties, distributed initial characterization”. These datasets were used for the analyses reported in a manuscript by Hall and Thompson (2021) in the Soil Science Society of America Journal.
Mass per tiller, nitrogen concentration, stable isotope ratios for carbon and nitrogen from the 1980-82 Eriophorum vaginatum reciprocal transplant experiment along a latitudinal gradient in interior Alaska collected in July, 2011
In 1980-1982, six transplant gardens were established along a latitudinal gradient in interior Alaska from Eagle Creek, AK in the south to Prudhoe Bay, AK in the north. Three sites, Toolik Lake (TL), Sagwon (SAG), and Prudhoe Bay (PB) are north of the continental divide and the remaining three, Eagle Creek (EC), No Name Creek (NN), and Coldfoot (CF), are south of the continental divide. Each garden consisted of 10 individual Eriophorum vaginatum tussocks transplanted back to their home-site, as well as 10 individuals from each of the other transplant sites. The gardens were harvested in 2011. Important variables are garden name, source population, mass per tiller, nitrogen concentration, and stable isotope ratios for Carbon and Nitrogen.
Light-saturated photosynthetic rate, dark respiration, stomatal conductance and ratio of internal to external carbon dioxide concentration from the 1980-82 Eriophorum vaginatum reciprocal transplant plots from Eagle Creek to Prudhoe Bay, Alaska, 2010
In 1980-1982, six transplant gardens were established along a latitudinal gradient in interior Alaska from Eagle Creek, AK, in the south to Prudhoe Bay, AK, in the north (Shaver et al. 1986) .Three sites, Toolik Lake (TL), Sagwon (SAG), and Prudhoe Bay (PB) are north of the continental divide and the remaining three, Eagle Creek (EC), No Name Creek (NN), and Coldfoot (CF), are south of the continental divide. Each garden consisted of 10 individual tussocks transplanted back to their home-site, as well as 10 individuals from each of the other transplant sites. Data were collected in July 2010 for tussocks transplanted in 1980-82 in a reciprocal transplant experiment and then harvested in 2011. Important variables are garden name, source population, light-saturated photosynthetic rate, dark respiration, stomatal conductance and ratio of internal to external carbon dioxide concentration.
Carbon and nitrogen isotopes and concentrations in terrestrial plants from a six-year (2006-2012) fertilization experiment at the Arctic LTER, Toolik Field Station, Alaska.
The data set describes stable carbon and nitrogen isotopes and carbon and nitrogen concentrations from an August 2012 pluck of a fertilization experiment begun in 2006. Fertilization was with nitrogen (N) and phosphorus (P). Fertilization levels included control, F2, F5, and F10, with F2 corresponding to yearly additions of 2 g/m2 N and 1 g/m2 P, F5 corresponding to yearly additions of 5 g/m2 N and 2.5 g/m2 P, and F10 corresponding to yearly additions of 10 g/m2 N and 5 g/m2 P. After harvest, plants were separated by species and then by tissue. Tissues were then dried, ground and analyzed for stable isotopes and concentrations at the University of New Hampshire stable isotope laboratory.
Plant and root biomass, nitrogen, carbon, and phosphorus concentrations in a mesic acidic tussock tundra experimental site established in 1981(MAT81) and harvested in 2015, Arctic LTER, Toolik Lake, Alaska.
Plant and root biomass, nitrogen, carbon, and phosphorus were measured in 2015 in the Arctic LTER tussock tundra experimental site (MAT81). This site was established in 1981 and has been harvested in previous years (see Shaver and Chapin Ecological Monographs, 61(1), 1991, pp.1-31, https://doi.org/10.2307/1942997). Data tables include the biomass for each harvested quadrat and block summaries for percent carbon, nitrogen, and phosphorus for control and fertilized plots from the original 4-block design. New control plots, established in 2015, are in a separate data table and include biomass, percent carbon, nitrogen, and phosphorus for each quadrat.
High-frequency dissolved organic carbon and nitrate from the Oksrukuyik Creek outlet near Toolik Field Station,Alaska, summer 2017-2019
Data file describing high frequency (every ~10 minutes), optial sensor-derived chemistry of river water from Oksukuyik Creek near Toolik Field Station, North Slope of Alaska. Data file includes date, time, dissolved organic carbon (DOC) concentration, and nitrate concentration. Sensors (V2 s::can uv-vis spectrophotometers) were continuously deployed from June through August or September and optically determined nitrate and dissolved organic carbon concentrations.
Carbon dioxide flux measurements and plot photographs from Arctic LTER Heath Tundra herbivore exclosures, Toolik Field Station, Alaska 2013
Ecosystem carbon dioxide (CO2) flux light response curves were measured from Arctic LTER heath tundra herbivore exclosures. Plot photographs were taken of each subplot using five consumer grade red, green and blue (RGB) wavelength camera. Structure from motion (SFM) photogrammetric method was then used to derive canopy structure. This file contains the CO2, normalized difference vegetation index (NDVI) data and photographs for each plot.
Modeling the effect of explicit vs implicit representation of grazing on ecosystem carbon and nitrogen cycling in response to elevated carbon dioxide and warming in arctic tussock tundra, Alaska - Dataset A
We use a simple model of coupled carbon and nitrogen cycles in terrestrial ecosystems to examine how explicitly representing grazers versus having grazer effects implicitly aggregated in with other biogeochemical processes in the model alters predicted responses to elevated carbon dioxide and warming. The aggregated approach can affect model predictions because grazer-mediated processes can respond differently to changes in climate from the processes with which they are typically aggregated. We use small-mammal grazers in arctic tundra as an example and find that the typical three-to-four-year cycling frequency is too fast for the effects of cycle peaks and troughs to be fully manifested in the ecosystem biogeochemistry. We conclude that implicitly aggregating the effects of small-mammal grazers with other processes results in an underestimation of ecosystem response to climate change relative to estimations in which the grazer effects are explicitly represented. The magnitude of this underestimation increases with grazer density. We therefore recommend that grazing effects be incorporated explicitly when applying models of ecosystem response to global change.
Modeling the effect of explicit vs implicit representation of grazing on ecosystem carbon and nitrogen cycling in response to elevated carbon dioxide and warming in arctic tussock tundra, Alaska - Dataset B
We use a simple model of coupled carbon and nitrogen cycles in terrestrial ecosystems to examine how explicitly representing grazers versus having grazer effects implicitly aggregated in with other biogeochemical processes in the model alters predicted responses to elevated carbon dioxide and warming. The aggregated approach can affect model predictions because grazer-mediated processes can respond differently to changes in climate from the processes with which they are typically aggregated. We use small-mammal grazers in arctic tundra as an example and find that the typical three-to-four-year cycling frequency is too fast for the effects of cycle peaks and troughs to be fully manifested in the ecosystem biogeochemistry. We conclude that implicitly aggregating the effects of small-mammal grazers with other processes results in an underestimation of ecosystem response to climate change relative to estimations in which the grazer effects are explicitly represented. The magnitude of this underestimation increases with grazer density. We therefore recommend that grazing effects be incorporated explicitly when applying models of ecosystem response to global change.
Steady state carbon, nitrogen, phosphorus, and water budgets for twelve mature ecosystems ranging from prairie to forest and from the arctic to the tropics
We use the Multiple Element Limitation (MEL) model to examine the responses of twelve ecosystems - from the arctic to the tropics and from grasslands to forests - to elevated carbon dioxide (CO2), warming, and 20% decreases or increases in annual precipitation. The ecosystems we simulated include moist acidic tundra, shrub tundra, and wet sedge tundra near Toolik Lake, Alaska, alpine dry meadow tundra near Niwot Ridge, Colorado, restored tallgrass prairie near Kellogg Biological Station, Michigan, native tallgrass prairie at the Konza Prairie, Kansas, upland and lowland boreal forest near Bonanza Creek, Alaska, temperate coniferous forest in HJ Andrews Experimental Forest, Oregon, a northern hardwood forest in Hubbard Brook Experimental Forest, New Hampshire, a transition oak-maple forest in Harvard Forest, Massachusetts, and lowland tropical rainforest near Caxiuanã National Forest, Pará, Brazil. For each of the twelve sites, we run six 100-year simulations beginning from the calibrated steady state (72 simulations total). The six simulations are: (1) increasing CO2 from 400 to 800 μmol mol-1, (2) warming from current temperatures to current plus 3.5oC, (3) decreasing precipitation from 100% to 80% of the current annual rate, (4) increasing precipitation from 100% to 120% of the current annual rate, (5) doubling of CO2, 3.5oC warming, and 20% decrease in precipitation, and (6) doubling of CO2, 3.5oC warming, and 20% increase in precipitation. The carbon, nitrogen, phosphorus, and water budgets presented here are used to calibrate the MEL model prior to running the climate change simulations. Citations and calculations for the data presented here are described in the individual site html files included in this dataset.
Ecosystem responses to changes in climate and carbon dioxide in twelve mature ecosystems ranging from prairie to forest and from the arctic to the tropics
We use the Multiple Element Limitation (MEL) model to examine the responses of twelve ecosystems - from the arctic to the tropics and from grasslands to forests - to elevated carbon dioxide (CO2), warming, and 20% decreases or increases in annual precipitation. The ecosystems we simulated include moist acidic tundra, shrub tundra, and wet sedge tundra near Toolik Lake, Alaska, alpine dry meadow tundra near Niwot Ridge, Colorado, restored tallgrass prairie near Kellogg Biological Station, Michigan, native tallgrass prairie at the Konza Prairie, Kansas, upland and lowland boreal forest near Bonanza Creek, Alaska, temperate coniferous forest in HJ Andrews Experimental Forest, Oregon, a northern hardwood forest in Hubbard Brook Experimental Forest, New Hampshire, a transition oak-maple forest in Harvard Forest, Massachusetts, and lowland tropical rainforest near Caxiuanã National Forest, Pará, Brazil. For each of the twelve sites, we run six 100-year simulations beginning from the calibrated steady state (72 simulations total). The six simulations are: (1) increasing CO2 from 400 to 800 μmol mol-1, (2) warming from current temperatures to current plus 3.5oC, (3) decreasing precipitation from 100% to 80% of the current annual rate, (4) increasing precipitation from 100% to 120% of the current annual rate, (5) doubling of CO2, 3.5oC warming, and 20% decrease in precipitation, and (6) doubling of CO2, 3.5oC warming, and 20% increase in precipitation. This dataset consists of the MEL model Windows executable, the driver and parameter file for each site, and the output files for each of the six simulations listed above.
Model Simulations of The Effects of Shifts in High-frequency Weather Variability (No Long-term Weather Trend) Control Carbon Loss from Land to the Atmosphere, Toolik Lake, Alaska, 2022-2122
Climate change is increasing extreme weather events, but effects on high-frequency weather variability and the resultant impacts on ecosystem function are poorly understood. We assessed ecosystem responses of arctic tundra to changes in day-to-day weather variability using a biogeochemical model and stochastic simulations of daily temperature, precipitation, and light. Changes in weather variability altered ecosystem carbon, nitrogen, and phosphorus stocks and cycling rates. Some responses of processes (e.g., respiration) were inconsistent with expectations, indicating that whole-ecosystem interactions and feedbacks moderate or even reverse responses to weather variability. More weather variability led to greater carbon losses from land to atmosphere, and less variability led to higher carbon sequestration on land. The magnitude of response to weather variability was similar to that predicted from climate mean trend effects. This dataset consists of the MEL parameter file, driver files and output files for simulations without a long term weather trend.
Model Simulations of The Effects of Shifts in High-frequency Weather Variability (With a Long-term Trend) on Carbon Loss from Land to the Atmosphere, Toolik Lake, Alaska, 2022-2122
Climate change is increasing extreme weather events, but effects on high-frequency weather variability and the resultant impacts on ecosystem function are poorly understood. We assessed ecosystem responses of arctic tundra to changes in day-to-day weather variability using a biogeochemical model and stochastic simulations of daily temperature, precipitation, and light. Changes in weather variability altered ecosystem carbon, nitrogen, and phosphorus stocks and cycling rates. Some responses of processes (e.g., respiration) were inconsistent with expectations, indicating that whole-ecosystem interactions and feedbacks moderate or even reverse responses to weather variability. More weather variability led to greater carbon losses from land to atmosphere, and less variability led to higher carbon sequestration on land. The magnitude of response to weather variability was similar to that predicted from climate mean trend effects. This dataset consists of the MEL parameter file, driver files and output files for simulations with a long-term weather trend.
Block summaries of biomass, carbon, nitrogen, and phosphorus allocation among tissue types, species, and plant functional types from Arctic LTER 1981 Moist Acidic Tussock (MAT81) long-term experiment harvests: 2000 and 2015, Toolik Lake Field Station, Alaska.
A complete accounting of biomass, C, N, and P allocation both among tissue types (leaves, stems, rhizomes, roots) and among species and plant functional types from Arctic LTER 1981 Moist Acidic Tussock (MAT81) long-term experiment’s untreated control plots and plots that were fertilized annually, harvested after 20 and 35 years, near Toolik Lake Field Station, Alaska. Data are gram per meter squared summarized by block.
Carbon flux from aquatic ecosystems of the Arctic Coastal Plain along the Beaufort Sea, Alaska, 2010-2018
Multiple aquatic ecosystems (pond, lake, river, lagoon, ocean) on the Arctic Coastal Plain (ACP) near Utqiaġvik, AK were visited to determine their relative contribution to landscape-level atmospheric CO2 flux and how this may have changed over time. pCO2 (partial pressure of carbon dioxide) was monitored in late summer (late July to mid-August) over a period of four years (2013, 2015, 2017, 2018) from open water areas and is related to habitat type, dissolved organic carbon (DOC) and environmental factors (temperature, radiation, rainfall). Data include both daily averages from most sites, as well as spatial representation of pCO2 in Elson Lagoon and diel cycles of pCO2 from a tundra pond. Pond NEP (net ecosystem production) is estimated by free water metabolism and presented as daily estimates over a four summer period.
Model estimates of runoff, dissolved organic carbon, soil temperature and moisture for Elson Lagoon watershed, Alaska, 1981-2020
This dataset contains model estimates of dissolved organic carbon (DOC) yield (mg C/m^2) and runoff (mm), for surface and subsurface flows, soil temperature (degree C), and soil moisture (% of soil volume) for grid cells spanning the Elson Lagoon watershed in northwest Alaska. Daily air temperature, precipitation, and wind speed data from Utqiagvik airport were used for meteorological forcings for the daily simulation by the Permafrost Water Balance Model (PWBM) from 1981 to 2020. The DOC and runoff data files are organized by grid cell and month. The soil temperature and soil moisture files are organized by grid cell and day of year (DOY), and contain values for the first eight model soil layers, with centers of the layers at 1, 3, 8, 13, 23, 33, 45, 55 cm depth. The estimates are most useful for analyses of the dynamics of the watershed’s surface and subsurface runoff and DOC yield. Leachate DOC concentrations can be obtained using the gridded runoff and yield values. A manuscript describing the data and associated analysis has been accepted for publication in Environmental Research Letters (Rawlins et al., 2021).
Eight Mile Lake Research Watershed, Carbon in Permafrost Experimental Heating Research (CiPEHR): Half-hourly growing season, chamber-based, CO2 flux data, 2009-2021
The Carbon in Permafrost Experimental Heating Research (CiPEHR) project addresses the following questions: 1) Does ecosystem warming cause a net release of C from the ecosystem to the atmosphere?, 2) Does the decomposition of old C, that comprises the bulk of the soil C pool, influence ecosystem C loss?, and 3) How do winter and summer warming alone, and in combination, affect ecosystem C exchange? We are answering these questions using a combination of field and laboratory experiments to measure ecosystem carbon balance and radiocarbon isotope ratios at a warming experiment located in an upland tundra field site near Healy, Alaska in the foothills of the Alaska Range. This data contains CO2 fluxes measured using an automated chamber system that measures net ecosystem CO2 exchange (NEE). Measurements are made every ~1.5 hours and modeled half-hourly. Half hour ecosystem respiration is modeled using an exponential Q10 relationship when light conditions are low (PAR<5umol/m2/s) and using a hyperbolic light relationship when PAR>5umol/m2/s. GPP is calculated as the difference between NEE and Reco.
Eight Mile Lake Research Watershed, Carbon in Permafrost Experimental Heating and Drying Research (DryPEHR): Growing season, chamber-based, CO2 flux data, 2009-2021
This drying and warming experiment addresses the following questions: 1) Does ecosystem drying, warming and permafrost thaw cause a net release or uptake of C from the ecosystem to the atmosphere?, 2) Does the decomposition of old C that comprises the bulk of the soil C pool influence ecosystem C loss? 3) How do drying and warming affect plant communities and ecosystem properties? We are answering these questions using a combined warming and drying experiment (DryPEHR), which is situated with the Carbon in Permafrost Experimental Heating Research (CiPEHR) project and located in an upland tundra field site near Healy, Alaska in the foothills of the Alaska Range. Warming treatment here refers to growing season air temperature warming (~1C) using open top chambers (OTC) combined with soil 'warming' using snow fences during the snow covered months. Drying is achieved using an automated pumping system that lowers the water table in the dry plots. Soil warming began in 2008; OTCs and drying in 2011. This data set includes measured values of CO2 fluxes during the growing season.
Eight Mile Lake Research Watershed, Carbon in Permafrost Experimental Heating Research (CiPEHR): Seasonal water table depth data, 2012-2024
The Carbon in Permafrost Experimental Heating Research (CiPEHR) project addresses the following questions: 1) Does ecosystem warming cause a net release of C from the ecosystem to the atmosphere?, 2) Does the decomposition of old C, that comprises the bulk of the soil C pool, influence ecosystem C loss?, and 3) How do winter and summer warming alone, and in combination, affect ecosystem C exchange? We are answering these questions using a combination of field and laboratory experiments to measure ecosystem carbon balance and radiocarbon isotope ratios at a warming experiment located in an upland tundra field site near Healy, Alaska in the foothills of the Alaska Range. This data includes water table depth measurements collected from winter warming and control treatment plots at CiPEHR for the ice-free period of 2024. Note that the experimental warming portion of this experiment concluded in 2022. These data are a continuation of measurements taken at previously warmed plots but plots were not actively manipulated in 2023 and 2024.
Aquatic biofilm autotrohic index, carbon dioxide flux, and environmental conditions for the APEX water table experiment 2021-2023
To better understand linkages between hydrology and ecosystem carbon flux in northern aquatic ecosystems, we evaluated the relationship between plant communities, biofilm development, and carbon dioxide (CO2) exchange following long-term changes in hydrology in an Alaskan fen. We quantified seasonal variation in biofilm composition and CO2 exchange in response to lowered and raised water-table position (relative to a control) during years with varying levels of background dissolved organic carbon (DOC). We then used nutrient-diffusing substrates to evaluate cause-effect relationships between changes in plant subsidies (i.e., leachates) and biofilm composition among water-table treatments. We found that background DOC concentration determined whether plant subsidies promoted net autotrophy or heterotrophy on nutrient diffusing substrates. In conditions where background DOC was <= 40 mg L-1, plant subsidies promoted an autotrophic biofilm. Conversely, when background DOC concentration was >= 50 mg L-1, plant subsidies promoted heterotrophy. Greater light attenuation associated with elevated levels of DOC may have overwhelmed the stimulatory effect of nutrients on autotrophic microbes by constraining photosynthesis while simultaneously allowing heterotrophs to outcompete autotrophs for available nutrients. At the ecosystem level, conditions that favored an autotrophic biofilm resulted in net CO2 uptake among all water-table treatments, whereas the site was a net source of CO2 to the atmosphere in conditions that supported greater heterotrophy. Taken together, these findings show that hydrologic history interacts with changes in dominant plant functional groups to alter biofilm composition, which has consequences for ecosystem CO2 exchange.
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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.