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At least 667 records · Page 37Linked to original sources

USGS1993

Conceptual evaluation of regional ground-water flow in the carbonate-rock province of the Great Basin, Nevada, Utah, and adjacent states

The regional groundwater flow system in the carbonate rocks of Nevada and Utah is conceptualized as shallow systems superimposed on deeper systems, which transmit water primarily through carbonate rocks. A computer model was used to simulate the two systems. The regional model includes simplifying assumptions that are probably valid for parts of the province; however, the validity of each assumption is unknown for the province as a whole. Therefore, simulation results do not perfectly replicate actual groundwater flow; instead they provide a conceptual evaluation of regional groundwater flow. The model was calibrated by adjusting transmissivity and vertical leakance until simulated water levels and simulated discharge generally agreed with known water levels, mapped areas of discharge, and estimates of discharge. Simulated flow is about 1.5 million acre-ft/yr. Most groundwater flow is simulated in the upper model layer where about 45 shallow flow regions were identified. In the lower layer, 17 deep-flow subregions were identified and grouped into 5 large regions on the basis of water-flow patterns. Simulated flow in this layer is about 28 percent of the total inflow and about half is discharged as springflow. Interbasin flow to several large springs is through thick, continuous, permeable carbonate rocks; elsewhere deep consolidated rocks are not highly transmissive, suggesting that carbonate rocks are not highly permeable everywhere or are not present everywhere. (USGS)

Nevada, Utah↗

USGS1996

Hydrogeologic assessment of shallow clastic and carbonate rock aquifers in Hendry and Collier counties, southwestern Florida

Direct-current electrical resistivity data were collected from 109 vertical electrical sounding sites in Hendry and Collier Counties, southwestern Florida. Selected direct-current electrical resistivity surveys, together with available borehole geologic and geophysical data, were used to determine the approximate areal extent of the shallow clastic aquifers composed of thick sands and carbonate lithologies. Results indicated that a complex pattern of shallow sands, clays, and carbonate lithologies occur throughout the area. Buried channel sands were found as deep as 50 meters below land surface in some places. The channels contain unconsolidated fine- to medium-grained quartz sand interbedded with sandy limestone, shell fragments, and gray-green sandy clay. Both surface and borehole geophysical techniques with lithologic data were necessary to approximately locate and define layers that might behave as confining layers and to locate and define the extent of any buried sand aquifers. The borehole geophysical data were used to analyze the zones of higher resistivity. Direct-current electrical resistivity data indicated the approximate location of certain layer boundaries. The conjunctive use of natural gamma and short- and long-normal resistivity logs was helpful in determining lithologic effects. Geohydrologic sections were prepared to identify potential locations of buried channels and carbonates containing freshwater. Buried channel sands and carbonate rock sections were identified in the subsurface that potentially may contain freshwater supplies.

Florida↗

USGS2004

Determining sources of water and contaminants to wells in a carbonate aquifer near Martinsburg, Blair County, Pennsylvania, by use of geochemical indicators, analysis of anthropogenic contaminants, and simulation of ground-water flow

Water supply for the Borough of Martinsburg, Pa., is from two well fields (Wineland and Hershberger) completed in carbonate-bedrock aquifers in the Morrison Cove Valley. Water supply is plentiful; however, waters with high concentrations of nitrate are a concern. This report describes the sources of water and contaminants to the supply wells. A review of previous investigations was used to establish the aquifer framework and estimate aquifer hydraulic properties. Aquifer framework and simulation of ground-water flow in a 25-square-mile area using the MODFLOW model helped to further constrain aquifer hydraulic properties and identify water-source areas in the zone of contribution of ground water to the well fields. Flow simulation identified potential contaminant-source areas. Data on contaminants and geochemical characteristics of ground water at the well fields were compared to the results of flow simulation. The Woodbury Anticline controls the aquifer framework near the well fields and four carbonate-bedrock formations contain the primary aquifers. Three carbonate-bedrock aquifers of Ordovician age overlie the Gatesburg aquifer of Cambrian age on the flanks of the anticline. Fracture, not conduit, permeability was determined to be the dominant water-bearing characteristic of the bedrock. The horizontal hydraulic conductivity of the Gatesburg aquifer is about 36 feet per day. The other carbonate aquifers (Nittany/Stonehenge, Bellefonte/Axemann, and Coburn through Loysburg aquifers) overlying and flanking the Gatesburg aquifer have horizontal hydraulic conductivities of about 1 foot per day. Regional directions of ground-water flow are toward the major streams with Clover Creek as the major discharge point for ground water in the east. Ground-water flow to the well fields is anisotropic with a 5:1 preferential horizontal direction along strike of the axial fold of the anticline. Thus, the zone of contribution of ground water to the well fields is elongate in a north-south direction along the anticline axis, with the majority of the flow to the well fields originating from the south. Human activity in the areal extent of the zone of contribution to the well fields was the source of contaminants. The areal extent of the zone of contribution included both urban areas in the Borough and a large amount of agricultural land. By relating results of flow simulation, natural geochemistry, and analyses of anthropogenic (human-made) contaminants, the source areas for water and contaminants were determined with more confidence than by using only flow simulation. Analysis of natural geochemistry identified water sources from both limestone and dolomite aquifers. Geochemistry results also indicated fractures, not conduits, were the dominant source of water from aquifers; however, quantitative source identification was not possible. Chemical ratios of chloride and bromide were useful to show that all samples of ground water had sources with chemical contributions from land surface. Nitrogen isotope ratio analysis indicated animal manure as the possible primary source of nitrate in most ground water. Some of the nitrate in ground water had chemical fertilizer as a source. At the Wineland well field, chemical fertilizer was likely the source of nitrate. The nitrate in water from the Hershberger well field was from a mixture of fertilizer and animal-manure sources. Human sewage was ruled out as a major source of nitrate in water from the municipal wells by results showing 1) wastewater compounds in sewage were rarely detected and 2) a mass-balance calculation indicating the small contribution of nitrogen that could be attributed to septic systems.

Scientific Investigations Report↗

USGS2005

Hydrogeology and simulation of source areas of water to production wells in a colluvium-mantled carbonate-bedrock aquifer near Shippensburg, Cumberland and Franklin Counties, Pennsylvania

This report presents the results of a study by the U.S. Geological Survey in cooperation with the Shippensburg Borough Authority to evaluate the source areas of water to production wells in a colluvium-mantled carbonate-bedrock aquifer in Cumberland and Franklin Counties, Pa. The areal extent of the zone of contribution was simulated for three production wells near Shippensburg, Pa. by use of a ground-water-flow model. A 111-square-mile area was selected as the model area and includes areas of the South Mountain Section and the Great Valley Section of the Valley and Ridge Physiographic Province. Within the model area, the geologic units in the South Mountain area are predominantly metamorphic rocks and the geologic units in the Great Valley are predominantly carbonate rocks. Hydrologic and geologic information were compiled to establish a conceptual model of ground-water flow. Characteristics of aquifer materials were determined, and streamflow and water levels were measured. Streamflow measurements in November 2003 showed all streams lost water as they flowed from South Mountain over the colluvium-mantled carbonate aquifer into the Great Valley. Some streams lost more than 1 cubic foot per second to the aquifer in this area. The Shippensburg Borough Authority owns three production wells in the model area. Two wells, Cu 969 and Fr 823, are currently (2004) used as production wells and produce 500,000 and 800,000 gallons per day, respectively. Well Cu 970 is intended to be brought on line as a production well in the future. Water levels were measured in 43 wells to use for model calibration. Water-level fluctuations and geophysical logs indicated confined conditions in well Cu 970. Ground-water flow was simulated with a model that consisted of two vertical layers, with five zones in each layer. The units were hydrostratigraphic units that initially were based on geologic formations, but boundaries were adjusted during model calibration. Model calibration resulted in a root mean square error of 9.8 feet. A parameter-estimation package was used during model calibration to estimate three parameters. The parameter estimation resulted in a value of 233 feet per day for horizontal hydraulic conductivity of the highly fractured carbonate rocks and sandy colluvium in layer 1; 3.97 feet per day for horizontal hydraulic conductivity of the ridge-forming unit in layer 1; and a value of 1.73 for horizontal anisotropy in both layers. The calibrated model was used to delineate the areal extent of the zone of contribution for wells Cu 969 and Fr 823. Although well Cu 970 is not currently (2004) being used, the areal extent of its zone of contribution also was simulated without additional model calibration. The shape of the areal extent of the zone of contribution was similar for each well and included an area that extended from the well southwest along the Tomstown Formation, and then extended southeast into the metamorphic rocks of South Mountain. The contributing areas from the watersheds of losing streams were also delineated because losing stream reaches bisect the areal extent of the zones of contribution. Spatial uncertainty of the areal extent of the zone of contribution was illustrated using a Monte-Carlo analysis. The model was run 1,000 times using randomly generated parameter sets that were normally distributed within the confidence interval around the optimal values for the three estimated parameters. The model converged and had a reasonable water budget for 980 of the model runs. For each of those 980 model runs, the recharge area was determined, and the results for all runs were compiled and contoured. The results of the Monte-Carlo analysis were compared to the results of the deterministic model, illustrating that the deterministic model has the greatest certainty in the area closest to each well in the Tomstown Formation. The areas farther from the well, upgradient, and in the metamorphic rocks have a higher degree

Pennsylvania↗

USGS2007

Water-Quality Constituents, Dissolved-Organic-Carbon Fractions, and Disinfection By-Product Formation in Water from Community Water-Supply Wells in New Jersey, 1998-99

Water samples were collected from 20 community water-supply wells in New Jersey to assess the chemical quality of the water before and after chlorination, to characterize the types of organic carbon present, and to determine the disinfection by-product formation potential. Water from the selected wells previously had been shown to contain concentrations of dissolved organic carbon (DOC) that were greater than 0.2 mg/L. Of the selected wells, five are completed in unconfined (or semi-confined) glacial-sediment aquifers of the Piedmont and Highlands (New England) Physiographic Provinces, five are completed in unconfined bedrock aquifers of the Piedmont Physiographic Province, and ten are completed in unconsolidated sediments of the Coastal Plain Physiographic Province. Four of the ten wells in the Coastal Plain are completed in confined parts of the aquifers; the other six are in unconfined aquifers. One or more volatile organic compounds (VOCs) were detected in untreated water from all of the 16 wells in unconfined aquifers, some at concentrations greater than maximum contaminant levels. Those compounds detected included aliphatic compounds such as trichloroethylene and 1,1,1-trichloroethane, aromatic compounds such as benzene, the trihalomethane compound, chloroform, and the gasoline additive methyl tert-butyl ether (MTBE). Concentrations of sodium and chloride in water from one well in a bedrock aquifer and sulfate in water from another exceeded New Jersey secondary standards for drinking water. The source of the sulfate was geologic materials, but the sodium and chloride probably were derived from human inputs. DOC fractions were separated by passing water samples through XAD resin columns to determine hydrophobic fractions from hydrophilic fractions. Concentrations of hydrophobic acids were slightly lower than those of combined hydrophilic acids, neutral compounds, and low molecular weight compounds in most samples. Water samples from the 20 wells were adjusted to a pH of 7, dosed with sodium hypochlorite, and incubated for 168 hours (seven days) at 25 ?C to form disinfection by-products (DBPs). Concentrations of the DBPs-trihalomethanes, haloacetic acids, haloacetonitriles, and chlorate-were measured. Concentrations of these compounds, with few exceptions, were higher in water from Coastal Plain wells than from wells in glacial and bedrock aquifers. The organic-carbon fractions were dosed with sodium hypochlorite, incubated for 168 hours at 25 ?C, and analyzed for trihalomethanes, haloacetic acids, haloacetonitriles, and chlorate. Concentrations of trihalomethanes and haloacetic acids were higher in most of the hydrophobic organic-acid fractions than in the hydrophilic fractions, with the highest concentrations in samples from Coastal Plain aquifers. Traces of haloacetonitriles were measured, mostly in the hydrophilic fraction. The aromaticity of the precursor DOC, as estimated by measurements of the absorbance of ultraviolet light at 254 nanometers, apparently is a factor in the DBP formation potentials determined, as aromaticity was greater in the samples that developed high concentrations of DBPs. VOCs may have contributed to the organic carbon present in some of the samples, but much of the DOC present in water from the 20 wells appeared to be natural in origin. The sediments of the Coastal Plain aquifers, in particular, contain substantial amounts of organic matter, which contribute ammonia, organic nitrogen, and aromatic DOC compounds to the ground water. Thus, the geologic characteristics of the aquifers appear to be a major factor in the potential for ground water to form DBPs when chlorinated.

Scientific Investigations Report↗

USGS1951

The quantitative determination of calcite associated with the carbonate-bearing apatites

The CO 2 combined as calcite in carbonate-bearing apatites as been distinguished from that combined as carbonate-apatite, or present in some form other than calcite, by use of X-ray powder patterns, differential thermal analyses, and differential solubility tests. These methods were applied to several pure apatite minerals, to one fossil bone, and to a group of phosphorites from the Phosphoria formation of Permian age from Trail Canyon and the Conda mine, Idaho, and the Laketown district, Utah. With the exceptions of pure fluorapatite, pure carbonate-flueorapatite, and one phosphorite from Trail Canyon, these substances contain varying amounts of calcite, but in all the samples an appreciable part of the carbonite content is not present as calcite. The results of solubility tests, in which the particle size of sample and the length of solution time were varied, imply that the carbonate content is not due to shielded calcite entrapped along an internal network of surfaces.

Idaho;Utah↗

USGS2012

Determination of the δ 13 C of dissolved inorganic carbon in water; RSIL lab code 1710

The purpose of the Reston Stable Isotope Laboratory (RSIL) lab code 1710 is to present a method to determine the δ 13 C of dissolved inorganic carbon (DIC) of water. The DIC of water is precipitated using ammoniacal strontium chloride (SrCl 2 ) solution to form strontium carbonate (SrCO 3 ). The δ 13 C is analyzed by reacting SrCO 3 with 100-percent phosphoric acid (H 3 PO 4 ) to liberate carbon quantitatively as carbon dioxide (CO 2 ), which is collected, purified by vacuum sublimation, and analyzed by dual inlet isotope-ratio mass spectrometry (DI-IRMS). The DI-IRMS is a DuPont double-focusing mass spectrometer. One ion beam passes through a slit in a forward collector and is collected in the rear collector. The other measurable ion beams are collected in the front collector. By changing the ion-accelerating voltage under computer control, the instrument is capable of measuring mass/charge ( m/z ) 45 or 46 in the rear collector and m/z 44 and 46 or 44 and 45, respectively, in the front collector. The ion beams from these m/z values are as follows: m/z 44 = CO 2 = 12 C 16 O 16 O, m/z 45 = CO 2 = 13 C 16 O 16 O primarily, and m/z 46 = CO 2 = 12 C 16 O 18 O primarily. The data acquisition and control software calculates δ 13 C values.

Techniques and Methods↗

USGS2004

Sources and Transport of Nutrients, Organic Carbon, and Chlorophyll-a in the San Joaquin River Upstream of Vernalis, California, during Summer and Fall, 2000 and 2001

Oxidizable materials from the San Joaquin River upstream of Vernalis can contribute to low dissolved oxygen episodes in the Stockton Deep Water Ship Channel that can inhibit salmon migration in the fall. The U.S. Geological Survey collected and analyzed samples at four San Joaquin River sites in July through October 2000 and June through November 2001, and at eight tributary sites in 2001. The data from these sites were supplemented with data from samples collected and analyzed by the University of California at Davis at three San Joaquin River sites and eight tributary sites as part of a separate study. Streamflows in the San Joaquin River were slightly above the long-term average in 2000 and slightly below average in 2001. Nitrate loads at Vernalis in 2000 were above the long-term average, whereas loads in 2001 were close to average. Total nitrogen loads in 2000 were slightly above average, whereas loads in 2001 were slightly below average. Total phosphorus loads in 2000 and 2001 were well below average. These nutrient loads correspond with the flow-adjusted concentration trends--nitrate concentrations significantly increased since 1972 (p < 0.01), whereas total nitrogen and total phosphorus concentrations did not (p > 0.05). Loading rates of nutrients and dissolved organic carbon increased in the San Joaquin River in the fall with the release of wetland drainage into Mud Slough and with increased reservoir releases on the Merced River. During August 2000 and September 2001, the chlorophyll-a loading rates and concentrations in the San Joaquin River declined and remained low during the rest of the sampling period. The most significant tributary sources of nutrients were the Tuolumne River, Harding Drain, and Mud Slough. The most significant tributary sources of dissolved organic carbon were Salt Slough, Mud Slough, and the Tuolumne and Stanislaus Rivers. Compared with nutrients and dissolved organic carbon, the tributaries were minor sources of chlorophyll-a, suggesting that most of the chlorophyll-a was produced in the San Joaquin River rather than its tributaries. On the basis of the carbon-to-nitrogen ratios and the d13C of particulate organic matter in the San Joaquin River and tributaries, the particulate organic matter in the river was mostly phytoplankton. On the basis of the d15N values of the particulate organic matter, and of total dissolved nitrogen and nitrate, the nitrate in the San Joaquin River probably was a significant nutrient source for the phytoplankton. The range of d15N and d18O values of nitrate in the San Joaquin River and tributaries suggest that animal waste or sewage was a significant source of nitrate in the river at the time the samples were collected.

Water-Resources Investigations Report↗

USGS1978

Interpretation of well logs in a carbonate aquifer

This report describes the log analysis of the Randolph and Sabial core holes in the Edwards aquifer in Texas, with particular attention to the principles that can be applied generally to any carbonate system. The geologic and hydrologic data were obtained during the drilling of the two holes, from extensive laboratory analysis of the cores, and from numerous geophysical logs run in the two holes. Some logging methods are inherently superiors to others for the analysis of limestone and dolomite aquifers. Three such systems are the dentistry, neutron, and acoustic-velocity (sonic) logs. Most of the log analysis described here is based on the interpretation of suites of logs from these three systems. In certain instances, deeply focused resistivity logs can be used to good advantage in carbonate rock studies; this technique is used to computer the water resistivity in the Randolph core hole. The rocks penetrated by the Randolph core hole are typical of those carbonates that have undergone very little solution by recent ground-water circulation. There are few large solutional openings; the water is saline; and the rocks are dark, dolomitic, have pore space that is interparticle or intercrystalline, and contain unoxidized organic material. The total porosity of rocks in the saline zone is higher than that of rocks in the fresh-water aquifer; however, the intrinsic permeability is much less in the saline zone because there are fewer large solutional openings. The Sabinal core hole penetrates a carbonate environment that has experienced much solution by ground water during recent geologic time. The rocks have high secondary porosities controlled by sedimentary structures within the rock; the water is fresh; and the dominant rock composition is limestone. The relative percentages of limestone and dolomite, the average matrix (grain) densities of the rock mixtures , and the porosity of the rock mass can be calculated from density, neutron, and acoustic logs. With supporting data from resistivity logs, the formation water quality can be estimated, as well as the relative cementation or tortuosity of the rock. Many of these properties calculated from logs can be verified by analysis of the core available from test holes drilled in the saline and fresh water zones.

Texas↗

USGS1979

Analytical method for dissolved-organic carbon fractionation

A standard procedure for analytical-scale dissolved organic carbon fractionation is presented, whereby dissolved organic carbon in water is first fractionated by a nonionic macroreticular resin into acid, base, and neutral hydrophobic organic solute fractions, and next fractionated by ion-exchange resins into acid, base, and neutral hydrophilic solute fractions. The hydrophobic solutes are defined as those sorbed on a nonionic, acrylic-ester macroreticular resin and are differentiated into acid, base, and nautral fractions by sorption/desorption controlled by pH adjustment. The hydrophilic bases are next sorbed on strong-acid ion-exchange resin, followed by sorption of hydrophilic acids on a strong-base ion-exchange resin. Hydrophilic neutrals are not sorbed and remain dissolved in the deionized water at the end of the fractionation procedure. The complete fractionation can be performed on a 200-milliliter filtered water sample, whose dissolved organic carbon content is 5-25 mg/L and whose specific conductance is less than 2,000 μmhos/cm at 25°C. The applications of dissolved organic carbon fractionation analysis range from field studies of changes of organic solute composition with synthetic fossil fuel production, to fundamental studies of the nature of sorption processes.

Water-Resources Investigations Report↗

USGS1998

Water-quality assessment of the Ozark Plateaus study unit, Arkansas, Kansas, Missouri, and Oklahoma — Nutrients, bacteria, organic carbon, and suspended sediment in surface water, 1993-95

Nutrient, bacteria, organic carbon, and suspended- sediment samples were collected from 1993-95 at 43 surface-water-quality sampling sites within the Ozark Plateaus National Water- Quality Assessment Program study unit. Most surface-water-quality sites have small or medium drainage basins, near-homogenous land uses (primarily agricultural or forest), and are located predominantly in the Springfield and Salem Plateaus. The water-quality data were analyzed using selected descriptive and statistical methods to determine factors affecting occurrence in streams in the study unit. Nitrogen and phosphorus fertilizer use increased in the Ozark Plateaus study unit for the period 1965-85, but the application rates are well below the national median. Fertilizer use differed substantially among the major river basins and physiographic areas in the study unit. Livestock and poultry waste is a major source of nutrient loading in parts of the study unit. The quantity of nitrogen and phosphorus from livestock and poultry wastes differed substantially among the river basins of the study unit's sampling network. Eighty six municipal sewage-treatment plants in the study unit have effluents of 0.5 million gallons per day or more (for the years 1985-91). Statistically significant differences existed in surface-water quality that can be attributed to land use, physiography, and drainage basin size. Dissolved nitrite plus nitrate, total phosphorus, fecal coliform bacteria, and dissolved organic carbon concentrations generally were larger at sites associated with agricultural basins than at sites associated with forested basins. A large difference in dissolved nitrite plus nitrate concentrations occurred between streams draining basins with agricultural land use in the Springfield and Salem Plateaus. Streams draining both small and medium agricultural basins in the Springfield Plateau had much larger concentrations than their counterparts in the Salem Plateau. Drainage basin size was not a significant factor in affecting total phosphorus, fecal coliform bacteria, or dissolved organic carbon concentrations. Suspended-sediment concentrations generally were small and indicative of the clear water in streams in the Ozark Plateaus. A comparison of the dissolved nitrite plus nitrate, total phosphorus, and fecal coliform data collected at the fixed and synoptic sites indicates that generally the data for streams draining basins of similar physiography, land-use setting, and drainage basin size group together. Many of the variations are most likely the result of differences in percent agricultural land use between the sites being compared or are discharge related. The relation of dissolved nitrite plus nitrate, total phosphorus, and fecal coliform concentration to percent agricultural land use has a strong positive 2 Water-Quality Assessment-Nutrients, Bacteria, Organic Carbon, and Suspended Sediment in Surface Water, 1993-95 correlation, with percent agricultural land use accounting for between 42 and 60 percent of the variation in the observed concentrations.

Arkansas, Kansas, Missouri, Oklahoma↗

USGS1993

Organic carbon sources and sinks in San Francisco Bay: variability induced by river flow

Sources and sinks of organic carbon for San Francisco Bay (California, USA) were estimated for 1980. Sources for the southern reach were dominated by phytoplankton and benthic microalgal production. River loading of organic matter was an additional important factor in the northern reach. Tidal marsh export and point sources played a secondary role. Autochthonous production in San Francisco Bay appears to be less than the mean for temperate-zone estuaries, primarily because turbidity limits microalgal production and the development of seagrass beds. Exchange between the Bay and Pacific Ocean plays an unknown but potentially important role in the organic carbon balance. Interannual variability in the organic carbon supply was assessed for Suisun Bay, a northern reach subembayment that provides habitat for important fish species (delta smelt Hypomesus transpacificus and larval striped bass Morone saxatilus). The total supply fluctuated by an order of magnitude; depending on the year, either autochthonous sources (phytoplankton production) or allochthonous sources (riverine loading) could be dominant. The primary cause of the year-to-year change was variability of freshwater inflows from the Sacramento and San Joaquin rivers, and its magnitude was much larger than long-term changes arising from marsh destruction and point source decreases. Although interannual variability of the total organic carbon supply could not be assessed for the southern reach, year-to-year changes in phytoplankton production were much smaller than in Suisun Bay, reflecting a relative lack of river influence.

California↗

USGS2023

Dissolved organic carbon dynamics and fluxes in Mississippi-Atchafalaya deltaic system impacted by an extreme flood event and hurricanes: A multi-satellite approach using Sentinel-2/3 and Landsat-8/9 data

Transport of riverine and wetland-derived dissolved organic carbon (DOC) spanning tidal wetlands, estuaries, and continental shelf waters functionally connects terrestrial and aquatic carbon reservoirs, yet the magnitude and ecological significance of this variable and its spatiotemporal linkage remains uncertain for coastal deltaic regions, such as Mississippi River Delta Plain, which includes Mississippi (MR) and Atchafalaya (AR) rivers and estuaries with vast expanses of wetlands and coastal forests. We examined DOC dynamics and fluxes in this large river-dominated wetland-estuarine system for the period between 2019 and 2021 that included an extreme river flood event in 2019, two major hurricanes (Barry in 2019 and Ida in 2021), and cold front passage using an improved adaptive quasi-analytical algorithm (QAA-AD) applied to multi-satellite sensors (Sentinel 3A/B OLCI, Landsat-8/OLI and Sentinel-2A/B MSI) with varying spectral and spatial (10/30/300 m) resolutions. The DOC estimates from multi-satellite sensors in combination with water fluxes were used to assess DOC fluxes from two large rivers (MR and AR) and small channels across the delta plain. Overall, this system delivered a total of 6.7 Tg C yr -1 (1 Tg = 10 12 g) into the estuarine zone and the northern Gulf of Mexico (nGoM) during 2019. High DOC fluxes from the AR (1.3 Tg C yr -1 ) and MR (4.5 Tg C yr -1 ) were associated with the extreme flood event in 2019. Hurricanes that occurred in the study period also contributed to the wetland and estuarine DOC fluxes into continental shelf waters; for example, the passage of Hurricane Barry in July 2019, delivered over a 3-day period ~1.33 ×10 9 g DOC from Barataria Basin into the nGoM. Sentinel 2-MSI land and water classification revealed that Hurricane Ida eroded a total of 1.34×10 8 m 2 of marshes in middle Barataria Basin, converting those habitats into open water with 3.0 m inundation depth and high DOC concentrations (16.4 mg L -1 ), a potentially large DOC source to the coastal waters. Overall, storms and flood events are major sources of DOC flux that facilitate transport of upstream carbon as well as transformation of carbon in the wetlands, through the conversion of vegetated wetland to open water.

Louisiana↗

USGS2014

Spatio-temporal patterns and climate variables controlling of biomass carbon stock of global grassland ecosystems from 1982 to 2006

Grassland ecosystems play an important role in subsistence agriculture and the global carbon cycle. However, the global spatio-temporal patterns and environmental controls of grassland biomass are not well quantified and understood. The goal of this study was to estimate the spatial and temporal patterns of the global grassland biomass and analyze their driving forces using field measurements, Normalized Difference Vegetation Index (NDVI) time series from satellite data, climate reanalysis data, and a satellite-based statistical model. Results showed that the NDVI-based biomass carbon model developed from this study explained 60% of the variance across 38 sites globally. The global carbon stock in grassland aboveground live biomass was 1.05 Pg·C, averaged from 1982 to 2006, and increased at a rate of 2.43 Tg·C·y −1 during this period. Temporal change of the global biomass was significantly and positively correlated with temperature and precipitation. The distribution of biomass carbon density followed the precipitation gradient. The dynamics of regional grassland biomass showed various trends largely determined by regional climate variability, disturbances, and management practices (such as grazing for meat production). The methods and results from this study can be used to monitor the dynamics of grassland aboveground biomass and evaluate grassland susceptibility to climate variability and change, disturbances, and management.

Remote Sensing↗

USGS2018

A molecular investigation of soil organic carbon composition across a subalpine catchment

The dynamics of soil organic carbon (SOC) storage and turnover are a critical component of the global carbon cycle. Mechanistic models seeking to represent these complex dynamics require detailed SOC compositions, which are currently difficult to characterize quantitatively. Here, we address this challenge by using a novel approach that combines Fourier transform infrared spectroscopy (FT-IR) and bulk carbon X-ray absorption spectroscopy (XAS) to determine the abundance of SOC functional groups, using elemental analysis (EA) to constrain the total amount of SOC. We used this SOC functional group abundance (SOC-fga) method to compare variability in SOC compositions as a function of depth across a subalpine watershed (East River, Colorado, USA) and found a large degree of variability in SOC functional group abundances between sites at different elevations. Soils at a lower elevation are predominantly composed of polysaccharides, while soils at a higher elevation have more substantial portions of carbonyl, phenolic, or aromatic carbon. We discuss the potential drivers of differences in SOC composition between these sites, including vegetation inputs, internal processing and losses, and elevation-driven environmental factors. Although numerical models would facilitate the understanding and evaluation of the observed SOC distributions, quantitative and meaningful measurements of SOC molecular compositions are required to guide such models. Comparison among commonly used characterization techniques on shared reference materials is a critical next step for advancing our understanding of the complex processes controlling SOC compositions.

Soil Systems↗

USGS2014

The implications of microbial and substrate limitation for the fates of carbon in different organic soil horizon types of boreal forest ecosystems: a mechanistically based model analysis

The large amount of soil carbon in boreal forest ecosystems has the potential to influence the climate system if released in large quantities in response to warming. Thus, there is a need to better understand and represent the environmental sensitivity of soil carbon decomposition. Most soil carbon decomposition models rely on empirical relationships omitting key biogeochemical mechanisms and their response to climate change is highly uncertain. In this study, we developed a multi-layer microbial explicit soil decomposition model framework for boreal forest ecosystems. A thorough sensitivity analysis was conducted to identify dominating biogeochemical processes and to highlight structural limitations. Our results indicate that substrate availability (limited by soil water diffusion and substrate quality) is likely to be a major constraint on soil decomposition in the fibrous horizon (40–60% of soil organic carbon (SOC) pool size variation), while energy limited microbial activity in the amorphous horizon exerts a predominant control on soil decomposition (>70% of SOC pool size variation). Elevated temperature alleviated the energy constraint of microbial activity most notably in amorphous soils, whereas moisture only exhibited a marginal effect on dissolved substrate supply and microbial activity. Our study highlights the different decomposition properties and underlying mechanisms of soil dynamics between fibrous and amorphous soil horizons. Soil decomposition models should consider explicitly representing different boreal soil horizons and soil–microbial interactions to better characterize biogeochemical processes in boreal forest ecosystems. A more comprehensive representation of critical biogeochemical mechanisms of soil moisture effects may be required to improve the performance of the soil model we analyzed in this study.

Biogeosciences↗

USGS2016

Colored dissolved organic matter in shallow estuaries: relationships between carbon sources and light attenuation

Light availability is of primary importance to the ecological function of shallow estuaries. For example, benthic primary production by submerged aquatic vegetation is contingent upon light penetration to the seabed. A major component that attenuates light in estuaries is colored dissolved organic matter (CDOM). CDOM is often measured via a proxy, fluorescing dissolved organic matter (fDOM), due to the ease of in situ fDOM sensor measurements. Fluorescence must be converted to CDOM absorbance for use in light attenuation calculations. However, this CDOM–fDOM relationship varies among and within estuaries. We quantified the variability in this relationship within three estuaries along the mid-Atlantic margin of the eastern United States: West Falmouth Harbor (MA), Barnegat Bay (NJ), and Chincoteague Bay (MD/VA). Land use surrounding these estuaries ranges from urban to developed, with varying sources of nutrients and organic matter. Measurements of fDOM (excitation and emission wavelengths of 365 nm (±5 nm) and 460 nm (±40 nm), respectively) and CDOM absorbance were taken along a terrestrial-to-marine gradient in all three estuaries. The ratio of the absorption coefficient at 340 nm (m −1 ) to fDOM (QSU) was higher in West Falmouth Harbor (1.22) than in Barnegat Bay (0.22) and Chincoteague Bay (0.17). The CDOM : fDOM absorption ratio was variable between sites within West Falmouth Harbor and Barnegat Bay, but consistent between sites within Chincoteague Bay. Stable carbon isotope analysis for constraining the source of dissolved organic matter (DOM) in West Falmouth Harbor and Barnegat Bay yielded δ 13 C values ranging from −19.7 to −26.1 ‰ and −20.8 to −26.7 ‰, respectively. Concentration and stable carbon isotope mixing models of DOC (dissolved organic carbon) indicate a contribution of 13 C-enriched DOC in the estuaries. The most likely source of 13 C-enriched DOC for the systems we investigated is Spartina cordgrass. Comparison of DOC source to CDOM : fDOM absorption ratios at each site demonstrates the relationship between source and optical properties. Samples with 13 C-enriched carbon isotope values, indicating a greater contribution from marsh organic material, had higher CDOM : fDOM absorption ratios than samples with greater contribution from terrestrial organic material. Applying a uniform CDOM : fDOM absorption ratio and spectral slope within a given estuary yields errors in modeled light attenuation ranging from 11 to 33 % depending on estuary. The application of a uniform absorption ratio across all estuaries doubles this error. This study demonstrates that light attenuation coefficients for CDOM based on continuous fDOM records are highly dependent on the source of DOM present in the estuary. Thus, light attenuation models for estuaries would be improved by quantification of CDOM absorption and DOM source identification.

Biogeosciences↗

USGS2012

Carbon export by rivers draining the conterminous United States

Material exports by rivers, particularly carbon exports, provide insight to basin geology, weathering, and ecological processes within the basin. Accurate accounting of those exports is valuable to understanding present, past, and projected basin-wide changes in those processes. We calculated lateral export of inorganic and organic carbon (IC and OC) from rivers draining the conterminous United States using stream gaging and water quality data from more than 100 rivers. Approximately 90% of land area and 80% of water export were included, which enabled a continental-scale estimate using minor extrapolation. Total carbon export was 41–49 Tg C yr −1 . IC was >75% of export and exceeded OC export in every region except the southeastern Atlantic seaboard. The 10 largest rivers, by discharge, accounted for 66% of water export and carried 74 and 62% of IC and OC export, respectively. Watershed carbon yield for the conterminous United States was 4.2 and 1.3 g C m −2 yr −1 for IC and OC, respectively. The dominance of IC export was unexpected but is consistent with geologic models suggesting high weathering rates in the continental United States due to the prevalence of easily weathered sedimentary rock.

Inland Waters↗