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128 results for “carbon biomass”
Assembled file of spring annual averages of pelagic tunicate organic biomass as carbon from the Southern California region, 1951 - 2011.
Derived dataset of approximately a dozen measures of annual springtime biomass of pelagic tunicates since 1951 (ongoing). Enumeration of net-towed samples (salps, doliolids, appendicularians, and pyrosomes) are converted to organic carbon biomass using length-carbon relationships (original from the zooplankton dataspace). Reference for pelagic tunicate organic carbon is Lavaniegos and Ohman (2007).
Plant aboveground biomass carbon and nitrogen:Effect of Fire Frequency on Grassland Vegetation and Soils
The purpose of this experiment, begun in 1983 by Johannes Knops, is to determine what effect different fire frequencies have on grassland vegetation. This experiment is being conducted in field B. There are 4 different burn treatments: 1. plots burned every year 2. plots burned every other year 3. controls which are not burned 4. plots burned every fourth year There are 6 replicates of each treatment which were randomly assigned to the 24 plots. Plots are 8 by 8 meters and are placed in a 3 by 8 grid with 2 meter walkways. Plots are marked with colored rebar at each corner.
Litter biomass carbon nitrogen from water treatment plots:BioCON: Biodiversity, CO2, and Nitrogen
BioCON (Biodiversity, CO2, and Nitrogen) is an ecological experiment started in 1997 at the University of Minnesota's Cedar Creek Ecosystem Science Reserve. BioCON's goal is to explore the ways in which plant communities will respond to three environmental changes that are known to be occurring on a global scale: increasing nitrogen deposition, increasing atmospheric CO2, and decreasing biodiversity. Why Biodiversity, CO2, and Nitrogen? While there are many uncertainties in global change biology, there are also some well documented facts. Some of these are: 1. The amount of carbon dioxide (CO2) in the atmosphere is rising. Since the industrial revolution, the CO2 concentration in the atmosphere has increased from approximately 275 parts per million (ppm) to about 378 ppm today. This has been largely the result of fossil fuel burning. It is expected that CO2 levels will continue to rise, and that by the year 2050 these levels will be approximately 550 ppm. CO2 is the raw material for photosynthesis and is known to affect plant growth and development. 2. The amount of nitrogen moving through terrestrial ecosystems has increased in the recent past. While natural "background" levels of nitrogen fixation have remained constant, human additions to the system through fertilizer production and fossil fuel use have increased dramatically. Nitrogen is a key nutrient for plant growth and plays a critical role in plant community structure and composition in many environments. 3. Biodiversity levels are falling. While the research and data are not as complete as they are for CO2 and nitrogen, data indicate that the number of species globally, is being reduced. Perhaps more important for ecosystem function, diversity levels on local to regional scales have fallen due to land use change, biotic invasion and many other drivers. While much is known about how each of these factors affects ecosystem functioning, many questions remain. There is also little data on how these issues affe
The vertical distribution of soil microbial biomass carbon: A global dataset
<p>Soil microbial biomass carbon (SMBC) is important in regulating soil organic carbon (SOC) dynamics along soil profiles by mediating the decomposition and formation of SOC. The dataset is about the vertical distributions of SOC, SMBC, and soil microbial quotient (SMQ = SMBC/SOC) and their relations to environmental factors across five continents. Data are collected from literature, with a total of 289 soil profiles and 1040 observations in different soil layers compiled. The associated environment data were also collectd including climate, ecosystem types, and edaphic factors. More specifically, we develop this dataset by compiling data from 59 papers published in the Web of Sciene and the China National Knowledge Infrastructure from the year of 1970 to 2019. All the data included in this dataset meet two creteria: 1) there are at least three soil layers along a soil profile, and 2) soil MBC is measured using the fumigation extraction method. The data were obtained from tables and texts from literature directly, and the data in figures were extracted using GetData Graph digitizer software version 2.25. When climate and soil properties are not available from publications, we obtainted the data from the World Weather Information Service (https://worldweather.wmo.int/en/home.html) and SoilGrids at a spatial resolution of 250 meters (version 0.5.3, https://soilgrids.org).</p> <p>The units of all the variables are converted to the standard international units or commonly used ones and the values are converted correspondingly. For example, the value of soil organic matter (SOM) is converted to SOC using the equation (SOC = SOM × 0.58). Soil depth is calculated as the arithmetic mean value of the upper and lower boundaries for a given soil layer.</p> <p>This dataset can be used in predicting global SOC change along soil profiles using the multi-layer soil C models. It can also be used to analyse how soil microbial biomass changes with plant roots as well as the composition, structure, and functions of soil microbial communities along soil profiles at large spatial scales. This dataset offers opportunities to improve our prediction of SOC dynamics under global changes and to advance our understanding of the environmental controls.</p>
Data from: Woody plant biomass and carbon exchange depend on elephant-fire interactions across a productivity gradient in African savanna
Elephants and fire are individually well-known disturbance agents within savanna ecosystems, but their interactive role in governing tree-cover dynamics and savanna–forest biome boundaries remains unresolved. Of central importance are the mechanisms by which elephants vs. fire affect tree biomass and cover, and how – over long time periods – both factors interact with rainfall and soils to govern tree biomass and carbon dynamics. Here, we evaluated the response of woody vegetation to 56 years of fire manipulation in South Africa's Kruger National Park, with three fire regimes (annual, triennial and unburned) replicated across a productivity gradient and subject to two periods of contrasting elephant abundances (generated by the cessation of culling in 1994). Higher fire frequencies had a negative effect on woody biomass in the low-elephant period, but this effect was weak to negligible in the high-elephant period as the difference among fire treatments diminished. Moreover, elephants removed increasing amounts of woody biomass as productivity increased across study sites, but fire did not. We infer that elephant-induced tree mortality could overcome increases in woody-plant productivity, while fire-induced mortality alone could not. Elephants caused woody-plant carbon to shift from a sink to a source; this effect was independent of fire treatment, with highest rates of net carbon removal in the wettest and most productive site. Synthesis. Our results reveal a context-dependent interaction between fire and elephants as disturbance agents in savanna: the influence of fire on woody plants was sensitive to the abundance of elephants and diminished with increased plant productivity. In contrast, elephants were capable of shifting landscapes from relatively dense woodland to open savanna, even in unburned sites, and exerted strong impacts irrespective of site conditions and plant productivity.
Data from: Effects of carbon-based nanomaterials on seed germination, biomass accumulation and salt stress response of bioenergy crops
Bioenergy crops are an attractive option for use in energy production. A good plant candidate for bioenergy applications should produce a high amount of biomass and resist harsh environmental conditions. Carbon-based nanomaterials (CBNs) have been described as promising seed germination and plant growth regulators. In this paper, we tested the impact of two CBNs: graphene and multi-walled carbon nanotubes (CNTs) on germination and biomass production of two major bioenergy crops (sorghum and switchgrass). The application of graphene and CNTs increased the germination rate of switchgrass seeds and led to an early germination of sorghum seeds. The exposure of switchgrass to graphene (200 mg/l) resulted in a 28% increase of total biomass produced compared to untreated plants. We tested the impact of CBNs on bioenergy crops under salt stress conditions and discovered that CBNs can significantly reduce symptoms of salt stress imposed by the addition of NaCl into the growth medium. Using an ion selective electrode, we demonstrated that the concentration of Na+ ions in NaCl solution can be significantly decreased by the addition of CNTs to the salt solution. Our data confirmed the potential of CBNs as plant growth regulators for non-food crops and demonstrated the role of CBNs in the protection of plants against salt stress by desalination of saline growth medium.
Code to support 'Optimal elevations for afforestation and reforestation to enhance biomass carbon accumulation in the tropics'
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Self-sacrificing and self-supporting biomass carbon anode assisted water electrolysis for low-cost hydrogen production
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Fine-resolution global maps of root biomass carbon colonized by arbuscular and ectomycorrhizal fungi
<p><span>Despite the recognized importance of mycorrhizal associations in ecosystem functioning, the actual abundance patterns of mycorrhizal fungi belowground are still unknown. This information is key for better quantification of mycorrhizal impacts on ecosystem processes and for incorporating mycorrhizal pathways into global biogeochemical models. Here we present the first high-resolution maps of fine root stocks colonized by arbuscular mycorrhizal (AM) and ectomycorrhizal (EcM) fungi (MgC ha−1). The maps were assembled by combining multiple open-source databases holding information on root biomass carbon, the proportion of AM and EcM tree biomass, plot-level relative abundance of plant species and intensity of AM and EcM root colonization. We calculated root-associated AM and EcM abundance in 881 spatial units, defined as the combination of ecoregions and land cover types across six continents. These maps serve as a basis for future research where continuous spatial estimates of root mycorrhizal stocks are needed.</span></p>
Data from: Woody plant biomass and carbon exchange depend on elephant-fire interactions across a productivity gradient in African savanna
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Data from: Measuring biomass and carbon stock in resprouting woody plants
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Data from: Opening the black box of plant nutrient uptake under warming predicts global patterns in community biomass and biological carbon storage
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Fine-resolution global maps of root biomass carbon colonized by arbuscular and ectomycorrhizal fungi
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Data from: Does plant biomass partitioning reflect energetic investments in carbon and nutrient foraging?
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Data from: Effects of carbon-based nanomaterials on seed germination, biomass accumulation and salt stress response of bioenergy crops
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A Compilation of Global Soil Microbial Biomass Carbon, Nitrogen, and Phosphorus Data
This data set provides the concentrations of soil microbial biomass carbon (C), nitrogen (N) and phosphorus (P), soil organic carbon, total nitrogen, and total phosphorus at biome and global scales. The data were compiled from a comprehensive survey of publications from the late 1970s to 2012 and include 3,422 data points from 315 papers. These data are from soil samples collected primarily at 0-15 cm depth with some from 0-30 cm. In addition, data were compiled for soil microbial biomass concentrations from soil profile samples to depths of 100 cm. Sampling site latitude and longitude were available for the majority of the samples that enabled assembling additional soil properties, site characteristics, vegetation distributions, biomes, and long-term climate data from several global sources of soil, land-cover, and climate data. These site attributes are included with the microbial biomass data. This data set contains two *.csv files of the soil microbial biomass C, N, P data. The first provides all compiled results emphasizing the full spatial extent of the data, while the second is a subset that provides only data from a series of profile samples emphasizing the vertical distribution of microbial biomass concentrations.There is a companion file, also in .csv format, of the references for the surveyed publications. A reference_number relates the data to the respective publication.The concentrations of soil microbial biomass, in combination with other soil databases, were used to estimate the global storage of soil microbial biomass C and N in 0-30 cm and 0-100 cm soil profiles. These storage estimates were combined with a spatial map of 12 major biomes (boreal forest, temperate coniferous forest, temperate broadleaf forest, tropical and subtropical forests, mixed forest, grassland, shrub, tundra, desert, natural wetland, cropland, and pasture) at 0.05-degree by 0.5-degree spatial resolution. The biome map and six estimates of C and N storage and C:N ration in soil microbial biomass are provided in a single netCDF format file.
Global Aboveground and Belowground Biomass Carbon Density Maps for the Year 2010
This dataset provides temporally consistent and harmonized global maps of aboveground and belowground biomass carbon density for the year 2010 at a 300-m spatial resolution. The aboveground biomass map integrates land-cover specific, remotely sensed maps of woody, grassland, cropland, and tundra biomass. Input maps were amassed from the published literature and, where necessary, updated to cover the focal extent or time period. The belowground biomass map similarly integrates matching maps derived from each aboveground biomass map and land-cover specific empirical models. Aboveground and belowground maps were then integrated separately using ancillary maps of percent tree cover and landcover and a rule-based decision tree. Maps reporting the accumulated uncertainty of pixel-level estimates are also provided.
Global 1-degree Maps of Forest Area, Carbon Stocks, and Biomass, 1950-2010
This data set provides global forest area, forest growing stock, and forest biomass data at 1-degree resolution for the period 1950-2010. The data set is based on a compilation of forest area and growing stock data reported in international assessments performed by FAO, MCPFE (now Forest Europe), and UNECE. Data of different assessments are to the extent possible harmonized to reflect both forest area and other wooded land, to be comparable between countries and assessments.
Forest Aboveground Biomass and Carbon Sequestration Potential, Northeastern USA
This dataset provides 90 m estimates of forest aboveground biomass (Mg/ha) for nominal 2011 and projections of carbon sequestration potential for 11 states in the Regional Greenhouse Gas Initiative (RGGI) domain. The RGGI is a cooperative, market-based effort among States in the eastern United States. Estimated biomass and sequestration potential were computed using the Ecosystem Demography (ED) model. The ED Model integrates several key data including climate variables from Daymet and MERRA2 products; physical soil and hydraulic properties from Probabilistic Remapping of SSURGO (POLARIS) and CONUS-SOIL; land cover characteristics from airborne lidar, the National Agriculture Imagery Program (NAIP), and the National Land Cover Database (NLCD); and vegetation parameters from the Forest Inventory and Analysis (FIA) Program.
Forest Aboveground Biomass and Carbon Sequestration Potential for Maryland, USA.
This dataset provides 90-m resolution maps of estimated forest aboveground biomass (Mg/ha) for nominal year 2011 and projections of carbon sequestration potential for the state of Maryland. Estimated biomass and sequestration potential were computed using the Ecosystem Demography (ED) model, which integrates data from multiple sources, including: climate variables from the North American Regional Reanalysis (NARR) Product, soil variables from the Soil Survey Geographic Database (SSURGO), land cover variables from airborne lidar, the National Agriculture Imagery Program (NAIP) and the National Land Cover Database (NLCD), and vegetation parameters from the Forest Inventory and Analysis (FIA) Program.
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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.