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Paul E. Stackelberg

Publications and source records attributed to Paul E. Stackelberg.

At least 37 records · Page 2Linked to original sources

Groundwater-quality and select quality-control data from the National Water-Quality Assessment Project, January through December 2015, and previously unpublished data from 2013 to 2014

Groundwater-quality data were collected from 502 wells as part of the National Water-Quality Assessment Project of the U.S. Geological Survey National Water-Quality Program and are included in this report. Most of the wells (500) were sampled from January through December 2015, and 2 of them were sampled in 2013. The data were collected from five types of well networks: principal aquifer study networks, which are used to assess the quality of groundwater used for public water supply; land-use study networks, which are used to assess land-use effects on shallow groundwater quality; major aquifer study networks, which are used to assess the quality of groundwater used for domestic supply; enhanced trends networks, which are used to evaluate the time scales during which groundwater quality changes; and vertical flow-path study networks, which are used to evaluate changes in groundwater quality from shallow to deeper depths. Groundwater samples were analyzed for a large number of water-quality indicators and constituents, including major ions, nutrients, trace elements, volatile organic compounds, pesticides, radionuclides, and some constituents of special interest (arsenic speciation, chromium [VI], and perchlorate). These groundwater-quality data, along with data from quality-control samples, are tabulated in this report and in an associated data release. Some data from environmental samples collected in 2013 and quality-control samples collected in 2014 also are included in the associated data release; these data are associated with networks described in this report and have not been published previously.

Data Series↗

Radium mobility and the age of groundwater in public-drinking-water supplies from the Cambrian-Ordovician aquifer system, north-central USA

High radium (Ra) concentrations in potable portions of the Cambrian-Ordovician (C-O) aquifer system were investigated using water-quality data and environmental tracers ( 3 H, 3 He trit , SF 6 , 14 C and 4 He rad ) of groundwater age from 80 public-supply wells (PSWs). Groundwater ages were estimated by calibration of tracers to lumped parameter models and ranged from modern (<50 yr) in upgradient, regionally unconfined areas to ancient (>1 Myr) in the most downgradient, confined portions of the potable system. More than 80 and 40 percent of mean groundwater ages were older than 1000 and 50,000 yr, respectively. Anoxic, Fe-reducing conditions and increased mineralization develop with time in the aquifer system and mobilize Ra into solution resulting in the frequent occurrence of combined Ra (Ra c = 226 Ra + 228 Ra) at concentrations exceeding the USEPA MCL of 185 mBq/L (5 pCi/L). The distribution of the three Ra isotopes comprising total Ra (Ra t = 224 Ra + 226 Ra + 228 Ra) differed across the aquifer system. The concentrations of 224 Ra and 228 Ra were strongly correlated and comprised a larger proportion of the Ra t concentration in samples from the regionally unconfined area, where arkosic sandstones provide an enhanced source for progeny from the 232 Th decay series. 226 Ra comprised a larger proportion of the Ra t concentration in samples from downgradient confined regions. Concentrations of Ra t were significantly greater in samples from the regionally confined area of the aquifer system because of the increase in 226 Ra concentrations there as compared to the regionally unconfined area. 226 Ra distribution coefficients decreased substantially with anoxic conditions and increasing ionic strength of groundwater (mineralization), indicating that Ra is mobilized to solution from solid phases of the aquifer as adsorption capacity is diminished. The amount of 226 Ra released from solid phases by alpha-recoil mechanisms and retained in solution increases relative to the amount of Ra sequestered by adsorption processes or co-precipitation with barite as adsorption capacity and the concentration of Ba decreases. Although 226 Ra occurred at concentrations greater than 224 Ra or 228 Ra, the ingestion exposure risk was greater for 228 Ra owing to its greater toxicity. In addition, 224 Ra added substantial alpha-particle radioactivity to potable samples from the C-O aquifer system. Thus, monitoring for Ra isotopes and gross-alpha-activity (GAA) is important in upgradient, regionally unconfined areas as downgradient, and GAA measurements made within 72 h of sample collection would best capture alpha-particle radiation from the short-lived 224 Ra.

Applied Geochemistry↗

Groundwater quality in the glacial aquifer system, United States

Groundwater provides nearly 50 percent of the Nation’s drinking water. To help protect this vital resource, the U.S. Geological Survey (USGS) National Water-Quality Assessment (NAWQA) Project assesses groundwater quality in aquifers that are important sources of drinking water (Burow and Belitz, 2014). The glacial aquifer system constitutes one of the important areas being evaluated.

Glacial Aquifer System↗

Groundwater quality in the Cambrian-Ordovician aquifer system, midwestern United States

Groundwater provides nearly 50 percent of the Nation’s drinking water. To help protect this vital resource, the U.S. Geological Survey (USGS) National Water-Quality Assessment (NAWQA) Project assesses groundwater quality in aquifers that are important sources of drinking water (Burow and Belitz, 2014). The Cambrian-Ordovician aquifer system constitutes one of the important areas being evaluated.

Illinois, Indiana, Iowa, Michigan, Minnesota, Miss↗

Groundwater-quality data from the National Water-Quality Assessment Project, January through December 2014 and select quality-control data from May 2012 through December 2014

Groundwater-quality data were collected from 559 wells as part of the National Water-Quality Assessment Project of the U.S. Geological Survey National Water-Quality Program from January through December 2014. The data were collected from four types of well networks: principal aquifer study networks, which are used to assess the quality of groundwater used for public water supply; land-use study networks, which are used to assess land-use effects on shallow groundwater quality; major aquifer study networks, which are used to assess the quality of groundwater used for domestic supply; and enhanced trends networks, which are used to evaluate the time scales during which groundwater quality changes. Groundwater samples were analyzed for a large number of water-quality indicators and constituents, including major ions, nutrients, trace elements, volatile organic compounds, pesticides, radionuclides, and some constituents of special interest (arsenic speciation, chromium [VI] and perchlorate). These groundwater-quality data, along with data from quality-control samples, are tabulated in this report and in an associated data release.

Data Series↗

Regression models for estimating concentrations of atrazine plus deethylatrazine in shallow groundwater in agricultural areas of the United States

Tobit regression models were developed to predict the summed concentration of atrazine [6-chloro- N -ethyl- N' -(1-methylethyl)-1,3,5-triazine-2,4-diamine] and its degradate deethylatrazine [6-chloro- N -(1-methylethyl)-1,3,5,-triazine-2,4-diamine] (DEA) in shallow groundwater underlying agricultural settings across the conterminous United States. The models were developed from atrazine and DEA concentrations in samples from 1298 wells and explanatory variables that represent the source of atrazine and various aspects of the transport and fate of atrazine and DEA in the subsurface. One advantage of these newly developed models over previous national regression models is that they predict concentrations (rather than detection frequency), which can be compared with water quality benchmarks. Model results indicate that variability in the concentration of atrazine residues (atrazine plus DEA) in groundwater underlying agricultural areas is more strongly controlled by the history of atrazine use in relation to the timing of recharge (groundwater age) than by processes that control the dispersion, adsorption, or degradation of these compounds in the saturated zone. Current (1990s) atrazine use was found to be a weak explanatory variable, perhaps because it does not represent the use of atrazine at the time of recharge of the sampled groundwater and because the likelihood that these compounds will reach the water table is affected by other factors operating within the unsaturated zone, such as soil characteristics, artificial drainage, and water movement. Results show that only about 5% of agricultural areas have greater than a 10% probability of exceeding the USEPA maximum contaminant level of 3.0 &mu;g L -1 . These models are not developed for regulatory purposes but rather can be used to (i) identify areas of potential concern, (ii) provide conservative estimates of the concentrations of atrazine residues in deeper potential drinking water supplies, and (iii) set priorities among areas for future groundwater monitoring.

Journal of Environmental Quality↗

Persistence of pharmaceuticals and other organic compounds in chlorinated drinking water as a function of time

Ninety eight pharmaceuticals and other organic compounds (POOCs) that were amended to samples of chlorinated drinking-water were extracted and analyzed 1, 3, 6, 8, and 10 days after amendment to determine whether the total chlorine residual reacted with the amended POOCs in drinking water in a time frame similar to the residence time of drinking water in a water distribution system. Results indicated that if all 98 were present in the finished drinking water from a drinking-water treatment plant using free chlorine at 1.2 mg/L as the distribution system disinfectant residual, 52 POOCs would be present in the drinking water after 10 days at approximately the same concentration as in the newly finished drinking water. Concentrations of 16 POOCs would be reduced by 32% to 92%, and 22 POOCs would react completely with residual chlorine within 24 h. Thus, the presence of free chlorine residual is an effective means for transforming some POOCs during distribution.

Science of the Total Environment↗

Efficiency of conventional drinking-water-treatment processes in removal of pharmaceuticals and other organic compounds

Samples of water and sediment from a conventional drinking-water-treatment (DWT) plant were analyzed for 113 organic compounds (OCs) that included pharmaceuticals, detergent degradates, flame retardants and plasticizers, polycyclic aromatic hydrocarbons (PAHs), fragrances and flavorants, pesticides and an insect repellent, and plant and animal steroids. 45 of these compounds were detected in samples of source water and 34 were detected in samples of settled sludge and (or) filter-backwash sediments. The average percent removal of these compounds was calculated from their average concentration in time-composited water samples collected after clarification, disinfection (chlorination), and granular-activated-carbon (GAC) filtration. In general, GAC filtration accounted for 53% of the removal of these compounds from the aqueous phase; disinfection accounted for 32%, and clarification accounted for 15%. The effectiveness of these treatments varied widely within and among classes of compounds; some hydrophobic compounds were strongly oxidized by free chlorine, and some hydrophilic compounds were partly removed through adsorption processes. The detection of 21 of the compounds in 1 or more samples of finished water, and of 3 to 13 compounds in every finished-water sample, indicates substantial but incomplete degradation or removal of OCs through the conventional DWT process used at this plant.

Science of the Total Environment↗

Response to comment on “Persistence of pharmaceutical compounds and other organic wastewater contaminants in a conventional drinking-water-treatment plant”

The U.S. Geological Survey (USGS) and the Centers for Disease Control thank Dr. Till for her comments concerning our research ( Till, 2005 ) and welcome the opportunity to respond. The primary objective of our study was to evaluate the potential for organic wastewater-related contaminants (OWCs), including pharmaceuticals, to survive a conventional drinking-water-treatment process and persist in potable-water supplies ( Stackelberg et al., 2004 ). Our study was supported by two USGS laboratories: the National Water Quality Laboratory (NWQL), which provided the HPLC/ESI-MS and CLLE GC/MS data and the Ocala Water Quality and Research Laboratory (OWQRL), which provided the LC/MS data ( Stackelberg et al., 2004 ). Although discussed as distinct techniques by Dr. Till and indicated by differing acronyms to distinguish the laboratories producing the data, as described in our paper, the two LC/MS methods are very similar; they consist of a solid-phase extraction method with analysis of the extract produced using high-performance liquid chromatography coupled to an electrospray ionization mass spectrometer operated in the positive mode. The NWQL and OWQRL report ‘trace’ and ‘ultratrace’ determinations of analytes that provide significant benefit for describing the presence and fate of low-level contaminants. For mass spectral methods, an analyte is qualitatively identified by its retention time on the chromatographic column as well as the presence of two or more confirming ions with area ratios that match that of the reference standard compounds. Because of a recognized increased risk of false positives, these qualitative identification criteria are used in conjunction with abundant quality-control samples (detailed below) to confirm detection prior to making an estimate of the concentration. These qualitative identification criteria must be met before a compound is considered present (or detected) in a sample ( Oblinger Childress et al., 1999 ). When a compound has been qualitatively identified in an environmental sample (whether above or below its reporting level [RL]), it is assessed in context with associated field and laboratory blanks, field and laboratory replicates, and other data, such as appropriate laboratory reagent spikes. An environmental concentration is calculated only after determining that field and laboratory procedures did not contaminate the samples. The concentrations are then calculated from 5- to 8-point calibration curves using internal standard quantitation. Our lowest calibration standard is intentionally much lower than the RL, typically 10 times lower. The most abundant molecular or fragment ion is used for quantitation, and, for the two LC/MS methods, at least one, and where possible two, qualifier ions are used for confirmation. For the GC/MS method, with its greater degree of fragmentation, one quantitation and two qualifier ions are used. When any of the abovementioned qualitative identification criteria are not met, the analyte is considered not present and is reported as “less than” the RL.

Science of the Total Environment↗

Pesticides in the Nation's Streams and Ground Water, 1992–2001

This report is one of a series of publications, The Quality of Our Nation's Waters, that describe major findings of the NAWQA Program on water-quality issues of regional and national concern. This report presents evaluations of pesticides in streams and ground water based on findings for the first decadal cycle of NAWQA. 'Pesticides in the Nation's Streams and Ground Water, 1992-2001' greatly expands the analysis of pesticides presented in 'Nutrients and Pesticides,' which was the first report in the series and was based on early results from 1992 to 1995. Other reports in this series cover additional water-quality constituents of concern, such as volatile organic compounds and trace elements, as well as physical and chemical effects on aquatic ecosystems. Each report builds toward a more comprehensive understanding of regional and national water resources. The information in this series is intended primarily for those interested or involved in resource management, conservation, regulation, and policymaking at regional and national levels. In addition, the information might interest those at a local level who wish to know more about the general quality of streams and ground water in areas near where they live and how that quality compares with other areas across the Nation.

Circular↗

Development and application of a regression equation for estimating the occurrence of atrazine in shallow ground water beneath agricultural areas of the United States

Results from 52 ground-water studies throughout the United States were used to examine relations between the occurrence of atrazine in shallow ground water in agricultural settings and explanatory variables that describe the natural setting, agricultural-management practices, and the type and amount of development in each area. The explanatory variables that were found to be correlated with atrazine occurrence were soil-infiltration rates, presence of artificial drainage (tile drains or trenches), available water-holding capacity of soils, soil permeability, amount of study area using ground water for irrigation source (as percentage of total area), amount of agricultural land (as percentage of total area), and intensity of atrazine use. Ordinary least-squares regression equations that used one or more of these explanatory variables describe as much as 58 percent of the variation in atrazine-detection frequencies. Application of a multivariate equation to unmonitored agricultural areas across the conterminous United States illustrates that atrazine use alone is insufficient for estimating the occurrence of atrazine in shallow ground water. Instead, areas in which soil characteristics and agricultural-management practices favor the movement of water from land surface to the water table and that also have intensive atrazine use are the most vulnerable to atrazine contamination.

Scientific Investigations Report↗

Application of health-based screening levels to ground-water quality data in a state-scale pilot effort

A state-scale pilot effort was conducted to evaluate a Health-Based Screening Level (HBSL) approach developed for communicating findings from the U.S. Geological Survey (USGS) National Water-Quality Assessment Program in a human-health context. Many aquifers sampled by USGS are used as drinking-water sources, and water-quality conditions historically have been assessed by comparing measured contaminant concentrations to established drinking-water standards and guidelines. Because drinking-water standards and guidelines do not exist for many analyzed contaminants, HBSL values were developed collaboratively by the USGS, U.S. Environmental Protection Agency (USEPA), New Jersey Department of Environmental Protection, and Oregon Health & Science University, using USEPA toxicity values and USEPA Office of Water methodologies. The main objective of this report is to demonstrate the use of HBSL approach as a tool for communicating water-quality data in a human-health context by conducting a retrospective analysis of ground-water quality data from New Jersey. Another important objective is to provide guidance on the use and interpretation of HBSL values and other human-health benchmarks in the analyses of water-quality data in a human-health context. Ground-water samples collected during 1996-98 from 30 public-supply, 82 domestic, and 108 monitoring wells were analyzed for 97 pesticides and 85 volatile organic compounds (VOCs). The occurrence of individual pesticides and VOCs was evaluated in a human-health context by calculating Benchmark Quotients (BQs), defined as ratios of measured concentrations of regulated compounds (that is, compounds with Federal or state drinking-water standards) to Maximum Contaminant Level (MCL) values and ratios of measured concentrations of unregulated compounds to HBSL values. Contaminants were identified as being of potential human-health concern if maximum detected concentrations were within a factor of 10 of the associated MCL or HBSL (that is, maximum BQ value (BQmax) greater than or equal to 0.1) in any well type (public supply, domestic, monitoring). Most (57 of 77) pesticides and VOCs with human-health benchmarks were detected at concentrations well below these levels (BQmax less than 0.1) for all three well types; however, BQmax values ranged from 0.1 to 3,000 for 6 pesticides and 14 VOCs. Of these 20 contaminants, one pesticide (dieldrin) and three VOCs (1,2-dibromoethane, tetrachloroethylene, and trichloroethylene) both (1) were measured at concentrations that met or exceeded MCL or HBSL values, and (2) were detected in more than 10 percent of samples collected from raw ground water used as sources of drinking water (public-supply and (or) domestic wells) and, therefore, are particularly relevant to human health. The occurrence of multiple pesticides and VOCs in individual wells also was evaluated in a human-health context because at least 53 different contaminants were detected in each of the three well types. To assess the relative human-health importance of the occurrence of multiple contaminants in different wells, the BQ values for all contaminants in a given well were summed. The median ratio of the maximum BQ to the sum of all BQ values for each well ranged from 0.83 to 0.93 for all well types, indicating that the maximum BQ makes up the majority of the sum for most wells. Maximum and summed BQ values were statistically greater for individual public-supply wells than for individual domestic and monitoring wells. The HBSL approach is an effective tool for placing water-quality data in a human-health context. For 79 of the 182 compounds analyzed in this study, no USEPA drinking-water standards or guidelines exist, but new HBSL values were calculated for 39 of these 79 compounds. The new HBSL values increased the number of detected pesticides and VOCs with human-health benchmarks from 65 to 77 (of 97 detected compounds), thereby expanding the basis for interpreting contaminant-occu

Scientific Investigations Report↗

Frequently co‐occurring pesticides and volatile organic compounds in public supply and monitoring wells, southern New Jersey, USA

One or more pesticides were detected with one or more volatile organic compounds (VOCs) in more than 95% of samples collected from 30 public supply and 95 monitoring wells screened in the unconsolidated surficial aquifer system of southern New Jersey, USA. Overall, more than 140,000 and more than 3,000 unique combinations of pesticides with VOCs were detected in two or more samples from the supply and monitoring wells, respectively. More than 400 of these combinations were detected in 20% or more of the samples from the supply wells, whereas only 17 were detected in 20% or more of the samples from the monitoring wells. Although many constituent combinations detected in water from the supply and monitoring wells are similar, differences in constituent combinations also were found and can be attributed, in part, to differences in the characteristics of these two well types. The monitoring wells sampled during this study yield water that typically was recharged beneath a single land‐use setting during a recent, discrete time interval and that flowed along relatively short paths to the wells. Public supply wells, in contrast, yield large volumes of water and typically have contributing areas that are orders of magnitude larger than those of the monitoring wells. These large contributing areas generally encompass multiple land uses; moreover, because flow paths that originate in these areas vary in length, these wells typically yield water that was recharged over a large temporal interval. Water withdrawn from public supply wells, therefore, contains a mixture of waters of different ages that were recharged beneath various land‐use settings. Because public supply wells intercept water flowing along longer paths with longer residence times and integrate waters from a larger source area than those associated with monitoring wells, they are more likely to yield water that contains constituents that were used in greater quantities in the past, that were introduced from point sources, and/or that are derived from the degradation of parent compounds along extended flow paths.

New Jersey↗

Water quality data for selected wells in the Coastal Plain of New Jersey, 1996-98

Water-quality data were collected during 1996-98 for 217 wells in New Jersey and 3 wells in New York as part of the U. S. Geological Survey's National Water Quality Assessment Program. Samples were collected for five ground-water surveys that were designed to assess water quality in major aquifer systems, with an emphasis on recently recharged (shallow) ground water associated with present and recent human activities. This report (1) summarizes the hydrogeologic framework in the areas of data collection; (2) describes the objectives and procedures for designing each ground-water survey; (3) summarizes the procedures and protocols for data collec-tion, analysis, and quality control; and (4) lists the concentrations of inorganic constituents, volatile organic compounds, pesticides, nutrients, and trace elements present in the ground-water samples.

Open-File Report↗

Effects of land use and travel time on the distribution of nitrate in the Kirkwood-Cohansey aquifer system in southern New Jersey

Residents of the southern New Jersey Coastal Plain are increasingly reliant on the unconfined Kirkwood-Cohansey aquifer system for public water supply as a result of increasing population and restrictions on withdrawals from the deeper, confined aquifers. Elevated nitrate concentrations above background levels have been found in wells in the surficial aquifer system in agricultural and urban parts of this area. A three-dimensional steady-state ground-water-flow model of a 400-square-mile study area near Glassboro, New Jersey, was used in conjunction with particle tracking to examine the effects of land use and travel time on the distribution of nitrate in ground and surface water in southern New Jersey. Contributing areas and ground-water ages, or travel times, of water at ground-water discharge points (streams and wells) in the study area were simulated. Concentrations of nitrate were computed by linking land use and age-dependent nitrate concentrations in recharge to the discharge points. Median concentrations of nitrate in water samples collected during 1996 from shallow monitoring wells in different land-use areas were used to represent the concentration of nitrate in aquifer recharge since 1990. On the basis of upward trends in the use of nitrogen fertilizer, the concentrations of nitrate in aquifer recharge in agricultural and urban areas were assumed to have increased linearly from the background value in 1940 (0.07 mg/L as N) to the 1990 (2.5-14 mg/L as N) concentrations. Model performance was evaluated by comparing the simulation results to measured nitrate concentrations and apparent ground-water ages. Apparent ground-water ages at 32 monitoring wells in the study area determined from tritium/helium-3 ratios and sulfur hexafluoride concentrations favorably matched simulated travel times to these wells. Simulated nitrate concentrations were comparable to concentrations measured in 27 water-supply wells in the study area. A time series (1987-98) of nitrate concentrations at base-flow conditions in three streams that drain basins of various sizes and with various land uses was compared to simulated concentrations in these streams. In all three of the streams, a reasonable fit to the measured concentrations was achieved by multiplying the simulated concentration by 0.6. Because nitrate appeared to move conservatively (not degraded or adsorbed) in ground water to wells, the apparent non-conservative behavior in streams indicates that about 40 percent of the nitrate in aquifer recharge is removed by denitrification in the aquifer near the streams and (or) by in-stream processes. The model was used to evaluate the effects of various nitrate management options on the concentration of nitrate in streams and water-supply wells. Nitrate concentrations were simulated under the following management alternatives: an immediate ban on nitrate input, reduction of input at a constant rate, and fixed input at the current (2000) level. The time required for water to move through the aquifer results in a time lag between the reduction of nitrate input in recharge and the reduction of nitrate concentration in streams and wells. In the gradual-reduction alternative, nitrate concentrations in streams and wells continued to increase for several years after the reduction was enacted. In both the immediate-ban and gradual-reduction alternatives, nitrate concentrations remained elevated above background concentrations long after nitrate input ceased. In the fixed-use alternative, concentrations in streams and wells continued to increase for 30 to 40 years before reaching a constant level. The spatial distributions of simulated nitrate concentrations in streams in 2000 and 2050 were examined with the assumption of no change in land use, nitrate concentration in recharge, or ground-water withdrawals. As expected, nitrate concentrations were highest in agricultural areas and lowest in largely undeveloped areas.

New Jersey↗

Comparison of nitrate, pesticides, and volatile organic compounds in samples from monitoring and public-supply wells, Kirkwood-Cohansey aquifer system, southern New Jersey

The number and total concentration of volatile organic compounds (VOCs) per sample were significantly greater in water from public-supply wells than in water from shallow and moderate-depth monitoring wells in the surficial Kirkwood-Cohansey aquifer system in the Glassboro area of southern New Jersey. In contrast, concentrations of nitrate (as nitrogen) and the number and total concentration of pesticides per sample were statistically similar in samples from shallow and moderate-depth monitoring wells and those from public-supply wells. VOCs in ground water typically are derived from point sources, which commonly exist in urban areas and which result in spatially variable contaminant concentrations near the water table. Because larger volumes of water are withdrawn from public-supply wells than from monitoring wells, their contributing areas are larger and, therefore, they are more likely to intercept water flowing from VOC point sources. Additionally, public-supply wells intercept flow paths that span a large temporal interval. Public-supply wells in the Glassboro study area withdraw water flowing along short paths, which contains VOCs that recently entered the aquifer system, and water flowing along relatively long paths, which contains VOCs that originated from the degradation of parent compounds or that are associated with past land uses. Because the volume of water withdrawn from monitoring wells is small and because shallow monitoring wells are screened near the water table, they generally intercept only relatively short flow paths. Therefore, samples from these wells represent relatively recent, discrete time intervals and contain both fewer VOCs and a lower total VOC concentration than samples from public-supply wells. Nitrate and pesticides in ground water typically are derived from nonpoint sources, which commonly are found in both agricultural and urban areas and typically result in lowlevel, relatively uniform concentrations near the water table. Because nonpoint sources are diffuse and because processes such as degradation or sorption/dispersion do not occur at rates sufficient to prevent detection of these constituents in parts of the aquifer used for domestic and public supply in the study area, concentrations of nitrate and pesticides and numbers of pesticide compounds are likely to be similar in samples from shallow monitoring wells and samples from public-supply wells. Results of a comparison of (1) the general characteristics of, and water-quality data from, public-supply wells in the Glassboro study area to available data from public-supply wells screened in the Kirkwood-Cohansey aquifer system outside the study area, and (2) land-use settings, soil characteristics, and aquifer properties in and outside the study area indicate that the findings of this study likely are applicable to the entire extent of the Kirkwood- Cohansey aquifer system in southern New Jersey.

New Jersey↗

Evaluation of the atmosphere as a source of volatile organic compounds in shallow groundwater

The atmosphere as a source of volatile organic compounds (VOCs) in shallow groundwater was evaluated over an area in southern New Jersey. Chloroform, methyl tertbutyl ether (MTBE), 1,1,1‐trichloroethane, tetrachloroethylene (PCE), and carbon disulfide (not a VOC) were detected frequently at low‐level concentrations in a network of 78 shallow wells in the surficial Kirkwood‐Cohansey aquifer system. The atmosphere was sampled for these compounds and only MTBE concentrations were high enough to potentially explain frequent detection in shallow groundwater. A mathematical model of reactive transport through the unsaturated zone is presented to explain how variations in unsaturated properties across the study area could explain differences in MTBE concentrations in shallow groundwater given the atmosphere as the source. Even when concentrations of VOCs in groundwater are low compared to regulatory concentration limits, it is critical to know the source. If the VOCs originate from a point source((), concentrations in groundwater could potentially increase over time to levels of concern as groundwater plumes evolve, whereas if the atmosphere is the source, then groundwater concentrations would be expected to remain at low‐level concentrations not exceeding those in equilibrium with atmospheric concentrations. This is the first analysis of VOC occurrence in shallow groundwater involving colocated atmosphere data.

Water Resources Research↗