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210 results for “soil nutrients”
Soil Characteristic and Nutrient Data from the Taylor Slough, within Everglades National Park (FCE), from March 2002 to April 2004
Three random soil cores are collected once a year from TS/Ph 1b, 2, 3, 4, 5, & 6b. The collection of these soil cores is in the dry season (Dec.-May). The top 10cm of soil is collected using a soil core. The soil is then analyzed to obtain its bulk density, organic matter content, TC, TN, and TP.
Soil Characteristics and Nutrient Data from the Shark River Slough, within Everglades National Park (FCE), from March 2003 to March 2004
Three random soil cores are collected once a year from SRS1b, SRS2, and SRS3. The collection of these soil cores is in the dry season (Dec.-May). The top 10cm of soil is collected using a soil core. The soil is then analyzed to obtain its bulk density, organic matter content, TC, TN, and TP.
H2Ohio Wetland Monitoring Program Surface Water and Soil Nutrient Content from Wetlands across Ohio, USA (2021–2022).
This data package contains surface water and soil nutrient concentration datasets from wetland projects across Ohio, USA monitored by the H2Ohio Wetland Monitoring Program. Monitoring began in May 2021 and is ongoing. This data package will be updated yearly. In general, surface water samples are collected to measure concentrations of major nutrients, including inorganic nitrogen, ammonium-nitrogen, total nitrogen, dissolved reactive phosphorus, and total phosphorus. Sampling from major inflows and outflows is prioritized at flow-through wetland projects to support the calculation of nutrient filtration estimates using mass balance approaches. Surface water samples may also be collected from representative zones or hydrologic features with sufficient standing water (i.e., vernal pools, vegetated areas, interconnected smaller pond-like areas, etc.) to assess nutrient conditions and processes within the wetland system. The majority of surface water sampling (~monthly) occurs from March through December, with opportunistic sampling in January and February. Every effort is made to collect samples during hydrologic events (i.e., storms) as well as baseflow conditions. Concurrent with surface water sampling, hand-held multiparameter sensors are used to measure snapshots of physicochemical characteristics including dissolved oxygen, temperature, specific conductance, turbidity, and pH. Soil samples (0-5 cm) are collected in saturated and unsaturated zones at each identified soil "patch" determined from expert opinion, soil maps (Natural Resources Conservation Service), and/or hydrogeophysical assessment. Additionally, soil samples may be collected along major visible hydrologic or elevation gradients. Soil sampling occurs 1-3 times a year in select wetland projects.
Microbial, Plant, and Soil Impacts on Soil Nutrient Cycling in Harvard Forest and Greater Boston 2021-2022
Microbes are the driving force behind nutrient cycling within soils, secreting enzymes necessary to break down organic matter, immobilizing nutrients and C, or transferring nutrients to plant hosts. Even though nutrients would almost never move through ecosystems without microbes, we know little about how their composition and activity is related to ecosystem nutrient cycling, and their importance relative to plant and soil abiotic factors. In this study, we sought to determine which commonly measured soil microbial community characteristics best explain soil N and P cycling, and the relative contributions of microbial, plant, and abiotic factors in explaining these processes.
Soil water content measurements and rainfall data for plots with experimentally altered precipitation and nutrient inputs at the Jornada Basin LTER site, 2011-ongoing
This dataset contains soil volumetric water content data collected starting in 2011 for a long-term precipitation and nutrient manipulation experiment at the Jornada Basin LTER site in southern New Mexico, U.S.A. This experiment uses precipitation shelters and irrigation treatments to manipulate water inputs, and fertilization treatments to alter nitrogen input to 2.5 x 2.5 meter plots in a desert grassland. Soil sensors are installed at surface and deep soil layers in each plot and collect hourly averages of volumetric water content using a time-domain reflectometry method. This dataset contains daily averages. This is an ongoing study and the dataset will be updated yearly.
Influence of soil amendment and crop species on nutrient cycling in a St. Paul urban garden, 2017-2023
An experiment was conducted from 2017-2023 at the University of St. Thomas research garden (Saint Paul, MN) to determine rates of nutrient recycling and loss from compost applied to urban gardens. Thirty-two 4 m2 study plots received one of six different soil amendment treatments, with four different crops growing on each plot. Meteorological data includes hourly measurements of rainfall, solar radiation, temperature and relative humidity, and wind speed and direction, from June 2017-October 2023. Hourly soil moisture measurements were recorded at depths of 10 cm, 20 cm, and 30 cm, from June-December 2021, June-October 2022, and June-October 2023. Annual crop harvest totals from each subplot are reported for 2017-2023. Leachate was collected from lysimeters installed in each of the 132 subplots weekly from June-October of each year (2017-2023), recording total volume. Leachate subsamples were analyzed for NO3-N, NH4-N, and PO4-P. Soil samples were collected at the beginning and end of the growing season in 2017, and every two weeks during the growing season from 2018-2023, and analyzed for pH, organic matter, Bray-1 extractable P, available K, nitrate, and ammonium, at the University of Minnesota Analytical Research Laboratory.
Soil organic carbon and nutrient dynamics in response to anaerobic digestate application to farm fields, Eastern Iowa, 2011-2023
This dataset documents a long-term, field-scale study of anaerobic digestate application on commercial croplands in eastern Iowa, USA. It includes detailed records of digestate composition, application rates, and timing, as well as soil test results collected over a 12-year period (2011–2023) from 14 agricultural fields. The dataset supports analysis of soil organic carbon (SOC), nutrient dynamics, and isotopic composition in response to digestate inputs. It contains 421 georeferenced soil samples, digestate nutrient profiles, field management histories, and spatial boundaries. The data were collected as part of a collaborative effort between researchers at Iowa State University and Sievers Family Farms to evaluate the agronomic and environmental implications of integrating anaerobic digestion into row crop and livestock systems.
Soil nutrient availability from the 2007 Anaktuvuk River, Alaska, USA fire scar during the 2016 growing season
This file contains plant-available nitrate (NO3), ammonium (NH4), and phosphate (PO4) in the upper 5-10 cm of organic matter from a burned and unburned site in the southern section of the 2007 Anaktuvuk River fire in northern Alaska. Soil nutrients were assessed using ion-exchange resin membranes incubated in the soil during the growing season of 2016.
Soil nutrient availability from the 2007 Anaktuvuk River, Alaska, USA fire scar during the 2019 growing season
This file contains plant-available nitrate (NO3), ammonium (NH4), phosphate (PO4), and total free primary amines (TFPA )in the upper 5-10cm of organic matter from a burned and unburned site in the southern section of the 2007 Anaktuvuk River fire in northern Alaska. Soil nutrients were assessed using buried resin bags which incubated for 1 month during the peak of the growing season in 2019.
Soil nutrients sampled in and around harvester ant nests in three habitats at the Jornada Basin LTER site, 1987
This dataset contains soil nutrient content measurements from harvester ant nests and reference soils in three nesting habitats at the Jornada Basin LTER site in 1987. The purpose of this investigation was to answer three general questions: 1. How does the modification of soil properties and the ratios of resources (e.g., water-N) by ants alter species assemblages of winter annual plants at the edge of the ant nests? 2. How does the "spring cleaning", clipping, predation or herbivory by ants affect success of the winter annual plants at the edge of ant nests? 3. Are there significant differences in the floristic assemblage and belowground standing crop (root biomass) between the edge of ant nest and the surrounding unaffected soils? Five ant nests and paired (non-nest) reference soils were sampled in three study locations. This dataset contains chemical analyses for the soil samples collected for each of the three sites, including total nitrogen, (ammonium, nitrate), inorganic phosphorus, and exchangeable cations (K+, Na+, Ca2+ and Mg2+). Also included is below ground biomass from five ant nests for each of the three sites. This study was completed in 1987.
Soil chemistry and nutrient distribution in long-term NPP plots at the Jornada Basin LTER site, 1989
This dataset contains soil nutrient and chemistry data from soils collected in 1989 at the 15 long-term NPP study sites at the Jornada Basin LTER site. The study sites were selected to represent the 5 major ecosystem types in the Chihuahuan Desert (upland grasslands, playa grasslands, mesquite-dominated shrublands, creosotebush-dominated shrublands, tarbush-dominated shrublands). For each ecosystem type, three sites were selected to represent the range in variability in production and plant diversity; thus the locations are not replicates. In 1989, replicate soil samples were collected at multiple depths from buffer zones surrounding the long-term vegetation monitoring plots. Nutrient and chemical analyses were subsequently performed on these soils, and the data here include inorganic nitrogen, phosphorus, pH, cation concentration, percent organic carbon, and other variables. This dataset is complete.
Soil chemistry and nutrient distribution in long-term NPP plots at the Jornada Basin LTER site, 1991
This dataset contains soil nutrient and chemistry data from soils collected in 1991 at the 15 long-term NPP study sites at the Jornada Basin LTER site. The study sites were selected to represent the 5 major ecosystem types in the Chihuahuan Desert (upland grasslands, playa grasslands, mesquite-dominated shrublands, creosotebush-dominated shrublands, tarbush-dominated shrublands). For each ecosystem type, three sites were selected to represent the range in variability in production and plant diversity; thus the locations are not replicates. In fall of 1991, replicate soil samples were collected at multiple spatial grid designs in the biomass plots of the long-term vegetation monitoring plots. Nutrient and chemical analyses were subsequently performed on these soils, and the data here include total nitrogen, pH, gravimetric water content, and other variables. This dataset is complete.
Shrub influence on soil moisture, nutrients, temperature and species composition, 2019 - 2020.
Shrubification, the expansion and densification of shrubs, is occurring in arctic and alpine zones across the globe (Myers-Smith et al., 2011). This alteration is primarily driven by warming temperatures (Elmendorf et al., 2012b, 2012a), and can have major consequences for the existing vegetation (Anthelme et al., 2007; Pajunen et al., 2011; Venn et al., 2014) and for nutrient pools (Sturm et al., 2005; DeMarco et al., 2014) due to the abiotic and biotic effects of shrubs. Shrubs accumulate snow which insulates the ground during the winter and provides more moisture later in the season (Liston et al., 2002). During the summer, shrubs provide shade and wind protection. Additionally, shrubs can increase the soil nitrogen (N) pool through their high input of plant material into the soil (DeMarco et al., 2014). These small-scale climatic and soil alterations have important consequences for plant community dynamics in the arctic and alpine. References: Anthelme, F., Villaret, J.-C., and Brun, J.-J., 2007: Shrub encroachment in the Alps gives rise to the convergence of sub-alpine communities on a regional scale. Journal of Vegetation Science, 18(3):355–362. DeMarco, J., Mack, M. C., and Bret-Harte, M. S., 2014: Effects of arctic shrub expansion on biophysical vs . biogeochemical drivers of litter decomposition. Ecological Society of America, 95(7):1861–1875. Elmendorf, S. C., Henry, G. H. R., Hollister, R. D., Björk, R. G., Bjorkman, A. D., Callaghan, T. V., Collier, L. S., Cooper, E. J., Cornelissen, J. H. C., Day, T. A., Fosaa, A. M., Gould, W. A., Grétarsdóttir, J., Harte, J., Hermanutz, L., Hik, D. S., Hofgaard, A., Jarrad, F., Jónsdóttir, I. S., Keuper, F., Klanderud, K., Klein, J. A., Koh, S., Kudo, G., Lang, S. I., Loewen, V., May, J. L., Mercado, J., Michelsen, A., Molau, U., Myers-Smith, I. H., Oberbauer, S. F., Pieper, S., Post, E., Rixen, C., Robinson, C. H., Schmidt, N. M., Shaver, G. R., Stenström, A., Tolvanen, A., Totland, Ø., Troxler, T., Wahren, C. H
Crab Burrows, Soil Nutrients, and Spartina alterniflora : organic content in Brownsville, VA 1992
The effect of Crab Burrows on Soil Nutrients and Spartina alterniflora by Winli Lin This study investigated the effects of fiddler crab (Uca pugnax) burrows on soil nutrients and the marsh grass Spartina alterniflora. Tall-form Spartina alterniflora (1-2m tall) typically dominates the marsh area that is flooded daily by tides. The short-form S. alterniflora(<0.5m tall) generally occupies the higher tidal heights (Bertness 1985). These short-form S. alterniflora are charterized by reduced soil drainage (Mendelssohn and Senecs 1980; Howes et al. 1981; Mendelssohn et al. 1981) and increased soil sulfide levels (King et al. 1982). From comparing control areas devoid of burrrows to those with burrows added, an increase in above-ground Spartina alterniflora production has been observed along with an increase of soil drainage rates and redox potential levels (Bertness 1985). Others have looked at how nutrient availability (Mendelssohn 1979) and sulfide accumulation (King et al. 1982; Howarth and Giblin 1983) may be the primary limiting factors controlling the production and success of S. alterniflora. While soil water movement has been shown to influence the soil parameters, (i.e., sulfide concentration and redox potential) that directly affect cordgrass production (King et al. 1982; Koch et al. 1990), little has been studied on how biotic modifications, such as crab burrows, mediate these physical factors. The Uca pugnax, are burrowing deposit-feeders that excavate and maintain semi-permanent burrows in the marsh surface. They have been found to not only oxygenate marsh soils (Howes et al 1981) and modify sediment meiofaunal abundance, they could also provide a suitable environment for continued burrowing and, as a byproduct, increase the marsh grass production and maintain the tall-form S. alterniflora. Uca pugnax, the mud fiddler crab, is the dominant form of crab seen in Brownsville, VA. Their burrows are primarily restricted to areas of tall-form S. alterniflora, due
Water-soluble organic matter and nutrients from stormwater control measure and urban wetland soils
Water-soluble organic matter (WSOM) represents organic matter that has the potential to be readily released from soils. WSOM has been understudied in urban, engineered soils relative to natural soils. To understand the potential for organic matter and nutrient release, we extracted WSOM from the soils of stormwater control measures (SCM) and urban wetlands. In February 2022, we sampled soils from 20 SCMs and natural wetlands in the Rappahannock River watershed of the mid-Atlantic United States. The SCMs reflected a variety of design configurations including bioretention, rain gardens, wet ponds, and swales. We also sampled naturally occurring floodplain wetlands that are located in this urban watershed. Soils were sampled to a depth of approximately 40 cm. If there was standing water present in the SCMs and wetlands at the time of sampling, we also collected surface water samples. If present, grab samples of leaf litter or biomass were collected. Soil characteristics, such as pH, bulk density, soil moisture, soil organic matter, and cation exchange capacity were also determined for each site. WSOM was extracted from soils and biomass in the laboratory and analyzed for organic matter concentration (dissolved organic carbon) and composition (absorbance and fluorescence metrics), along with dissolved nutrient concentrations (total dissolved nitrogen, total dissolved phosphorus, nitrate, ammonium, and orthophosphate). In addition to the 20 sites in the Rappahannock watershed, soils from 2 additional bioretention SCMs on the Virginia Tech campus were sampled on a monthly basis from February 2022 to February 2023 to explore temporal variability in WSOM. To characterize changes in soil hydrologic conditions during monthly SCM sampling, we applied a Thornthwaite-type monthly water balance model. Finally, we performed a simple scaling exercise to WSOM results based on SCM area, sample depth, and soil bulk density to estimate potential SCM contributions of organic matter.
Absorbed soil nutrients on ion exchange membranes in the reciprocal transplant gardens at Toolik Lake, Coldfoot, and Sagwon in 2016
Transplant gardens at Toolik Lake and Sagwon were established in 2014. At each location, 60 tussocks each from ecotypes of Eriophorum vaginatum from Coldfoot (CF, 67°15′32″N, 150°10′12″W), Toolik Lake (TL, 68°37′44″N, 149°35′0″W), and Sagwon (SG, 69°25′26″N, 148°42′49″W) were transplanted. At the reciprocal transplant gardens, ion exchange membranes were used to measure nutrient availability over two time periods: Early season (June) and mid season (July). Membranes were deployed in the field for either 20 or 21 days, depending on travel constraints.
Mangrove soil phosphorus addition experiment from June 2013 to August 2013 at the mangrove peat soil mesocosms (FCE), Key Largo, Florida - Nutrients in Porewater, Soil and Roots
Sea levels in South Florida are conservatively predicted to rise by 0.60 m by 2060. The key mechanisms that maintain coastal peatland elevation against increasing sea level are organic matter accumulation via plant production and mineral sedimentation rates (Smoak et al. 2013). Although coastal mangrove soils are regularly inundated with seawater, little is know about the drivers of carbon sequestration (above or below ground) versus atmospheric efflux under different conditions of salinity and elevated phosphorus (P) associated with sea-level rise and storm surge. A recent study using mangrove peat soils found that seawater inundation reduced soil carbon efflux losses and salinity concentration had little effect on carbon retention or loss pathways. The next logical steps are to understand how plant-soil interactions affect above and below ground carbon processes, as well as how increases in P associated with storm surge from the Gulf of Mexico will influence physical, chemical and biological components of mangrove soils that are associated with above and belowground carbon processes. We will manipulate P in inundated peat soil mesocosms with disturbed and undisturbed red mangrove (Rhizophora mangle) seedlings to identify some of the fundamental mechanisms of soil elevation and carbon cycling given expected increases in seawater-based P availability in South Florida coastal mangroves.
Mangrove soil phosphorus addition experiment from July 2013 to August 2013 at the mangrove peat soil mesocosms (FCE), Key Largo, Florida - Nutrients in Surface Water and Aboveground Biomass
Sea levels in South Florida are conservatively predicted to rise by 0.60 m by 2060. The key mechanisms that maintain coastal peatland elevation against increasing sea level are organic matter accumulation via plant production and mineral sedimentation rates (Smoak et al. 2013). Although coastal mangrove soils are regularly inundated with seawater, little is know about the drivers of carbon sequestration (above or below ground) versus atmospheric efflux under different conditions of salinity and elevated phosphorus (P) associated with sea-level rise and storm surge. A recent study using mangrove peat soils found that seawater inundation reduced soil carbon efflux losses and salinity concentration had little effect on carbon retention or loss pathways. The next logical steps are to understand how plant-soil interactions affect above and below ground carbon processes, as well as how increases in P associated with storm surge from the Gulf of Mexico will influence physical, chemical and biological components of mangrove soils that are associated with above and belowground carbon processes. We will manipulate P in inundated peat soil mesocosms with disturbed and undisturbed red mangrove (Rhizophora mangle) seedlings to identify some of the fundamental mechanisms of soil elevation and carbon cycling given expected increases in seawater-based P availability in South Florida coastal mangroves.
Sediment and nutrient deposition and plant-soil phosphorus interactions associated with Hurricane Irma (2017) in mangroves of the Florida Coastal Everglades (FCE LTER), Florida
We quantified how Hurricane Irma influenced soil nutrient pools, vertical accretion, and plant phosphorus (P) uptake after its passage across the Florida Coastal Everglades in September 2017. Mangrove leaf litter data from three years (2008, 2014, 2018) were selected for each site at Shark River estuary to identify species-specific foliar P responses post-Wilma’s impact in 2005 and immediate post-Irma’s impact in 2017. We also monitored porewater SRP concentrations in the Shark River mangrove sites to evaluate the effect of Hurricane Irma on soil chemistry. The data in this data package were used in the following paper: Castañeda-Moya, E., V.H. Rivera-Monroy, R.M. Chambers, X. Zhao, L. Lamb-Wotton, A. Gorsky, E.E. Gaiser, T.G. Troxler, J.S. Kominoski, and M. Hiatt. 2020. Hurricanes fertilize mangrove forests in the Gulf of Mexico (Florida Everglades, USA). PNAS. In Press.
NBC01 Konza Prairie Belowground Plot Experiment: Soil chemistry responses to experimental manipulations of fire, nutrients and mowing
To address the potential interactive effects of fire, aboveground biomass removal, and nutrient amendments on above- and belowground responses, a long-term field experiment was initiated in 1986 as part of the Konza Prairie Long-Term Ecological Research (LTER) program. The general goals of this experiment are: 1) to document both short- and long-term responses of plants and soils to fire, aboveground biomass removal (a surrogate for grazing in these small plots), and nutrient amendments (additions of N and/or P); and 2) to provide a better understanding of the mechanisms underlying tallgrass prairie responses to fire, aboveground biomass removal and nutrient enrichment. Effects of burning, mowing, and N + P additions on soil chemistry are measured on the 64 belowground plots at irregular intervals. Variables measured include P, NO3, NH4, Mn, Cu, K, Zn, Ca, Fe, Mg, Na, ph, Organic matter and Organic-N.
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