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John S. Zogorski

Publications and source records attributed to John S. Zogorski.

At least 19 recordsLinked to original sources

The atmosphere can be a source of certain water soluble volatile organic compounds in urban streams

Surface water and air volatile organic compound (VOC) data from 10 U.S. Geological Survey monitoring sites were used to evaluate the potential for direct transport of VOCs from the atmosphere to urban streams. Analytical results of 87 VOC compounds were screened by evaluating the occurrence and detection levels in both water and air, and equilibrium concentrations in water (C w s ) based on the measured air concentrations. Four compounds (acetone, methyl tertiary butyl ether, toluene, and m - & p -xylene) were detected in more than 20% of water samples, in more than 10% of air samples, and more than 10% of detections in air were greater than long-term method detection levels (LTMDL) in water. Benzene was detected in more than 20% of water samples and in more than 10% of air samples. Two percent of benzene detections in air were greater than one-half the LTMDL in water. Six compounds (chloroform, p-isopropyltoluene, methylene chloride, perchloroethene, 1,1,1-trichloroethane, and trichloroethene) were detected in more than 20% of water samples and in more than 10% of air samples. Five VOCs, toluene, m - & p -xylene, methyl tert-butyl ether (MTBE), acetone, and benzene were identified as having sufficiently high concentrations in the atmosphere to be a source to urban streams. MTBE, acetone, and benzene exhibited behavior that was consistent with equilibrium concentrations in the atmosphere.

Journal of the American Water Resources Associatio

Prioritization of constituents for national- and regional-scale ambient monitoring of water and sediment in the United States

A total of 2,541 constituents were evaluated and prioritized for national- and regional-scale ambient monitoring of water and sediment in the United States. This prioritization was done by the U.S. Geological Survey (USGS) in preparation for the upcoming third decade (Cycle 3; 2013–23) of the National Water-Quality Assessment (NAWQA) Program. This report provides the methods used to prioritize the constituents and the results of that prioritization. Constituents were prioritized by the NAWQA National Target Analyte Strategy (NTAS) work group on the basis of available information on physical and chemical properties, observed or predicted environmental occurrence and fate, and observed or anticipated adverse effects on human health or aquatic life. Constituents were evaluated within constituent groups that were determined on the basis of physical or chemical properties or on uses or sources. Some constituents were evaluated within more than one constituent group. Although comparable objectives were used in the prioritization of constituents within the different constituent groups, differences in the availability of information accessed for each constituent group led to the development of separate prioritization approaches adapted to each constituent group to make best use of available resources. Constituents were assigned to one of three prioritization tiers: Tier 1, those having the highest priority for inclusion in ambient monitoring of water or sediment on a national or regional scale (including NAWQA Cycle 3 monitoring) on the basis of their likelihood of environmental occurrence in ambient water or sediment, or likelihood of effects on human health or aquatic life; Tier 2, those having intermediate priority for monitoring on the basis of their lower likelihood of environmental occurrence or lower likelihood of effects on human health or aquatic life; and Tier 3, those having low or no priority for monitoring on the basis of evidence of nonoccurrence or lack of effects on human health or aquatic life, or of having insufficient evidence of potential occurrence or effects to justify placement into Tier 2. Of the 1,081 constituents determined to be of highest priority for ambient monitoring (Tier 1), 602 were identified for water and 686 were identified for sediment (note that some constituents were evaluated for both water and sediment). These constituents included various types of organic compounds, trace elements and other inorganic constituents, and radionuclides. Some of these constituents are difficult to analyze, whereas others are mixtures, isomers, congeners, salts, and acids of other constituents; therefore, modifications to the list of high-priority constituents for ambient monitoring could be made on the basis of the availability of suitable methods for preparation, extraction, or analysis. An additional 1,460 constituents were placed into Tiers 2 or 3 for water or sediment, including some constituents that had been placed into Tier 1 for a different matrix; 436 constituents were placed into Tier 2 for water and 246 constituents into Tier 2 for sediment; 979 constituents were placed into Tier 3 for water and 779 constituents into Tier 3 for sediment.

Scientific Investigations Report

Factors associated with sources, transport, and fate of chloroform and three other trihalomethanes in untreated groundwater used for drinking water

Multiple lines of evidence for indicating factors associated with the sources, transport, and fate of chloroform and three other trihalomethanes (THMs) in untreated groundwater were revealed by evaluating low-level analytical results and logistic regression results for THMs. Samples of untreated groundwater from wells used for drinking water were collected from 1996-2007 from 2492 wells across the United States and analyzed for chloroform, bromodichloromethane, dibromochloromethane, and bromoform by a low-level analytical method implemented in April 1996. Using an assessment level of 0.02 μg/L, chloroform was detected in 36.5% of public-well samples and 17.6% of domestic-well samples, with most concentrations less than 1 μg/L. Brominated THMs occurred less frequently than chloroform but more frequently in public-well samples than domestic-well samples. For both public and domestic wells, THMs occurred most frequently in urban areas. Logistic regression analyses showed that the occurrence of THMs was related to nonpoint sources such as urban land use and to point sources like septic systems. The frequent occurrence and concentration distribution pattern of THMs, as well as their frequent co-occurrence with other organic compounds and nitrate, all known to have anthropogenic sources, and the positive associations between THM occurrence and dissolved oxygen and recharge indicate the recycling of water that contains THMs and other anthropogenic contaminants.

Environmental Science & Technology

MTBE; to what extent will past releases contaminate community water supply wells?(Brief Article)

The increasing frequency of detection of the widely used gasoline additive methyl tertbutyl ether (MTBE) in both ground- and surface waters is receiving much attention from the media, environmental scientists, state environmental agencies, and federal agencies. At the national level, the September 15,1999, Report of the Blue Ribbon Panel on Oxygenates in Gasoline (i) )tates that between 5 and 10% of community drinking water supplies in high MTBE use areas show at least detectable concentrations of MTBE, and about 1% of those systems are characterized by levels of this compound that are above 20 pg/L. In Maine, a desire to determine the extent of MTBE contamination led to a 1998 study (2) that revealed that this compound is found at levels above 0.1 pg/L in 16% of 951 randomly selected household wells and in 16% of the 793 community water systems tested in that state (37 wells were not tested). The study also suggested that between 1400 and 5200 household wells may have levels above 35 pg/L, although no community water supplies were found to be above that concentration. For comparison, Maryland, New Hampshire, New York, and California have set MTBE remediation "action levels" at or below 20 pg/L, and EPA has set its advisory level for taste and odor at 20-40 pg/L (3).

Environmental Science & Technology

Design and evaluation of a field study on the contamination of selected volatile organic compounds and wastewater-indicator compounds in blanks and groundwater samples

The Field Contamination Study (FCS) was designed to determine the field processes that tend to result in clean field blanks and to identify potential sources of contamination to blanks collected in the field from selected volatile organic compounds (VOCs) and wastewater-indicator compounds (WICs). The VOCs and WICs analyzed in the FCS were detected in blanks collected by the U.S. Geological Survey (USGS) National Water-Quality Assessment (NAWQA) Program during 1996–2008 and 2002–08, respectively. To minimize the number of variables, the study required ordering of supplies just before sampling, storage of supplies and equipment in clean areas, and use of adequate amounts of purge-and-trap volatile-grade methanol and volatile pesticide-grade blank water (VPBW) to clean sampling equipment and to collect field blanks. Blanks and groundwater samples were collected during 2008–09 at 16 sites, which were a mix of water-supply and monitoring wells, located in 9 States. Five different sample types were collected for the FCS at each site: (1) a source-solution blank collected at the USGS National Water Quality Laboratory (NWQL) using laboratory-purged VPBW, (2) source-solution blanks collected in the field using laboratory-purged VPBW, (3) source-solution blanks collected in the field using field-purged VPBW, (4) a field blank collected using field-purged VPBW, and (5) a groundwater sample collected from a well. The source-solution blank and field-blank analyses were used to identify, quantify, and document extrinsic contamination and to help determine the sources and causes of data-quality problems that can affect groundwater samples. Concentrations of compounds detected in FCS analyses were quantified and results were stored in the USGS National Water Information System database after meeting rigorous identification and quantification criteria. The study also utilized information provided by laboratory analysts about evidence indicating the presence of selected compounds, using less rigorous identification criteria than is required for reporting data to the National Water Information System database. For the FCS, these data are considered adequate to indicate "evidence of presence," and were used only for diagnostic purposes. Evidence of VOCs and WICs at low concentrations near or less than the long-term method detection level can indicate a contamination problem that could affect future datasets if method detection levels were ever to be lowered.

Scientific Investigations Report

Quality of volatile organic compound data from groundwater and surface water for the National Water-Quality Assessment Program, October 1996–December 2008

This report describes the quality of volatile organic compound (VOC) data collected from October 1996 to December 2008 from groundwater and surface-water sites for the U.S. Geological Survey's National Water-Quality Assessment (NAWQA) Program. The VOC data described were collected for three NAWQA site types: (1) domestic and public-supply wells, (2) monitoring wells, and (3) surface-water sites. Contamination bias, based on the 90-percent upper confidence limit (UCL) for the 90th percentile of concentrations in field blanks, was determined for VOC samples from the three site types. A way to express this bias is that there is 90-percent confidence that this amount of contamination would be exceeded in no more than 10 percent of all samples (including environmental samples) that were collected, processed, shipped, and analyzed in the same manner as the blank samples. This report also describes how important native water rinsing may be in decreasing carryover contamination, which could be affecting field blanks. The VOCs can be classified into four contamination categories on the basis of the 90-percent upper confidence limit (90-percent UCL) concentration distribution in field blanks. Contamination category 1 includes compounds that were not detected in any field blanks. Contamination category 2 includes VOCs that have a 90-percent UCL concentration distribution in field blanks that is about an order of magnitude lower than the concentration distribution of the environmental samples. Contamination category 3 includes VOCs that have a 90-percent UCL concentration distribution in field blanks that is within an order of magnitude of the distribution in environmental samples. Contamination category 4 includes VOCs that have a 90-percent UCL concentration distribution in field blanks that is at least an order of magnitude larger than the concentration distribution of the environmental samples. Fifty-four of the 87 VOCs analyzed in samples from domestic and public-supply wells were not detected in field blanks (contamination category 1), and 33 VOC were detected in field blanks. Ten of the 33 VOCs had a 90-percent UCL concentration distribution in field blanks that was at least an order of magnitude lower than the concentration distribution in environmental samples (contamination category 2). These 10 VOCs may have had some contamination bias associated with the environmental samples, but the potential contamination bias was negligible in comparison to the environmental data; therefore, the field blanks were assumed to be representative of the sources of contamination bias affecting the environmental samples for these 10 VOCs. Seven VOCs had a 90-percent UCL concentration distribution of the field blanks that was within an order of magnitude of the concentration distribution of the environmental samples (contamination category 3). Sixteen VOCs had a 90-percent UCL concentration distribution in the field blanks that was at least an order of magnitude greater than the concentration distribution of the environmental samples (contamination category 4). Field blanks for these 16 VOCs appear to be nonrepresentative of the sources of contamination bias affecting the environmental samples because of the larger concentration distributions (and sometimes higher frequency of detection) in field blanks than in environmental samples. Forty-three of the 87 VOCs analyzed in samples from monitoring wells were not detected in field blanks (contamination category 1), and 44 VOCs were detected in field blanks. Eight of the 44 VOCs had a 90-percent UCL concentration distribution in field blanks that was at least an order of magnitude lower than concentrations in environmental samples (contamination category 2). These eight VOCs may have had some contamination bias associated with the environmental samples, but the potential contamination bias was negligible in comparison to the environmental data; therefore, the field blanks were assumed to be representative. Seven VOCs had a 90-percent UCL concentration distribution in field blanks that was of the same order of magnitude as the concentration distribution of the environmental samples (contamination category 3). Twenty-nine VOCs had a 90-percent UCL concentration distribution in the field blanks that was an order of magnitude greater than the distribution of the environmental samples (contamination category 4). Field blanks for these 29 VOCs appear to be nonrepresentative of the sources of contamination bias to the environmental samples. Fifty-four of the 87 VOCs analyzed in surface-water samples were not detected in field blanks (category 1), and 33 VOC were detected in field blanks. Sixteen of the 33 VOCs had a 90-percent UCL concentration distribution in field blanks that was at least an order of magnitude lower than the concentration distribution in environmental samples (contamination category 2). These 16 VOCs may have had some contamination bias associated with the environmental samples, but the potential contamination bias was negligible in comparison to the environmental data; therefore, the field blanks were assumed to be representative. Ten VOCs had a 90-percent UCL concentration distribution in field blanks that was similar to the concentration distribution of environmental samples (contamination category 3). Seven VOCs had a 90-percent UCL concentration distribution in the field blanks that was greater than the concentration distribution in environmental samples (contamination category 4). Field-blank samples for these seven VOCs appear to be nonrepresentative of the sources of contamination bias to the environmental samples. The relation between the detection of a compound in field blanks and the detection in subsequent environmental samples appears to be minimal. The median minimum percent effectiveness of native water rinsing is about 79 percent for the 19 VOCs detected in more than 5 percent of field blanks from all three site types. The minimum percent effectiveness of native water rinsing (10 percent) was for toluene in surface-water samples, likely because of the large detection frequency of toluene in surface-water samples (about 79 percent) and in the associated field-blank samples (46.5 percent). The VOCs that were not detected in field blanks (contamination category 1) from the three site types can be considered free of contamination bias, and various interpretations for environmental samples, such as VOC detection frequency at multiple assessment levels and comparisons of concentrations to benchmarks, are not limited for these VOCs. A censoring level for making comparisons at different assessment levels among environmental samples could be applied to concentrations of 9 VOCs in samples from domestic and public-supply wells, 16 VOCs in samples from monitoring wells, and 9 VOCs in surface-water samples to account for potential low-level contamination bias associated with these selected VOCs. Bracketing the potential contamination by comparing the detection and concentration statistics with no censoring applied to the potential for contamination bias on the basis of the 90-percent UCL for the 90th-percentile concentrations in field blanks may be useful when comparisons to benchmarks are done in a study. The VOCs that were not detected in field blanks (contamination category 1) from the three site types can be considered free of contamination bias, and various interpretations for environmental samples, such as VOC detection frequency at multiple assessment levels and comparisons of concentrations to benchmarks, are not limited for these VOCs. A censoring level for making comparisons at different assessment levels among environmental samples could be applied to concentrations of 9 VOCs in samples from domestic and public-supply wells, 16 VOCs in samples from monitoring wells, and 9 VOCs in surface-water samples to account for potential low-level contamination bias associated with these selected VOCs. Bracketing the potential contamination by comparing the detection and concentration statistics with no censoring applied to the potential for contamination bias on the basis of the 90-percent UCL for the 90th-percentile concentrations in field blanks may be useful when comparisons to benchmarks are done in a study.

Scientific Investigations Report

Methyl tert-butyl ether in ground and surface water of the United States: National-scale relations between MTBE occurrence in surface and ground water and MTBE use in gasoline

The detection frequency of methyl tert -butyl ether (MTBE) in ground and surface water of the United States is positively related to the content of MTBE in gasoline in various metropolitan areas of the U.S. The frequency of detection of MTBE is generally higher in areas that use larger amounts of MTBE in gasoline. Sampling of surface and ground water by the U.S. Geological Survey's National Water-Quality Assessment (NAWQA) Program between 1993 and 1998 revealed a frequent detection of low concentrations of MTBE. In this analysis, data from several national-scale gasoline surveys are examined and data from one survey that is most extensive in geographic and temporal coverage is used to relate the detection of MTBE in ground and surface water to the volumetric content of MTBE in gasoline.

ACS Symposium Series

Occurrence of volatile organic compounds in selected urban streams in the United States, 1995-2003

As part of the U.S. Geological Survey's (USGS) National Water-Quality Assessment (NAWQA) Program, urban indicator sites were monitored to (1) characterize the stream quality from drainage basins with predominantly residential and commercial land use, and (2) determine which selected natural and anthropogenic factors affect stream quality. A total of 869 water samples were collected from 37 urban streams during 1995-2003 and were analyzed for 87 volatile organic compounds (VOCs). The occurrence of VOCs in urban streams is described in this report for (1) all samples as a single dataset, (2) all samples grouped by streamflow pentiles, and (3) all samples grouped by warmer (April through September) and cooler (October through March) months by the detection frequency and (or) concentration of (a) any VOC, (b) VOC groups, and (c) individual compounds. An assessment level of 0.02 microgram per liter (ug/L) was used to compute the detection frequencies and concentrations of VOCs. Concentrations of VOCs were compared to (1) U.S. Environmental Protection Agency's (USEPA) drinking-water Maximum Contaminant Levels (MCLs) or Drinking Water Advisories, (2) Health-Based Screening Levels (HBSLs) developed by the USGS in collaboration with the USEPA and other agencies, and (3) USEPA and Canadian aquatic-life criteria. One or more VOCs were detected in 97.1 percent of 869 samples, and one or more VOCs were detected frequently (greater than 80 percent) at all sites. The median total VOC concentration for all samples was 0.57 ug/L, and total VOC concentrations in a single sample ranged from not detected to 698 ug/L. About 85 percent of the samples contained two or more VOCs, and about one-half contained five or more VOCs. The gasoline hydrocarbons were the most frequently occurring VOC group followed by solvents, trihalomethanes (THMs), gasoline oxygenates, organic synthesis compounds, fumigants, and refrigerants. Concentration ranges for most VOC groups were distributed over at least two orders of magnitude. Fifty-seven of the 87 VOCs analyzed were detected in at least one sample at an assessment level of 0.02 ug/L. More than one-half of the 30 VOCs not detected in samples were organic synthesis compounds. Fifteen compounds had detection frequencies greater than or equal to 10 percent. With the exception of toluene and chloroform, the median concentration of each VOC for all samples was less than the assessment level. Furthermore, the median concentrations of detections for the 15 most frequently occurring VOCs ranged from 0.03 to 3.9 ug/L, and typically were less than or equal to 0.10 ug/L. The 869 samples from the 37 sites were stratified into five streamflow pentiles (less than 20, 20-less than 40, 40-less than 60, 60-less than 80, and greater than or equal to 80 percent of estimated long-term streamflow statistics) for comparison of the occurrence of VOCs. The detection frequency of one or more VOCs by streamflow pentile varied only slightly from 96.7 to 97.7 percent. The median total VOC concentrations in samples for the five streamflow pentiles ranged from 0.39 to 1.0 ug/L. Two or more VOCs were present in more than 80 percent of samples in each of the five pentiles. The gasoline hydrocarbons, solvents, THMs, and gasoline oxygenates occurred frequently (greater than 30 percent) in all streamflow pentiles, in contrast to the organic synthesis compounds, fumigants, and refrigerants that occurred less frequently in urban streams under all streamflow conditions. The median total VOC concentrations for gasoline hydrocarbons, solvents, gasoline oxygenates, and organic synthesis compounds generally increased as streamflow increased. In contrast, the median total VOC concentrations for THMs and fumigants generally decreased as streamflow increased. The median total VOC concentrations for refrigerants showed no pattern as streamflow increased. Because differences between VOC occurrence and streamflow pentiles were small for most compariso

Scientific Investigations Report

Occurrence and potential human-health relevance of volatile organic compounds in drinking water from domestic wells in the United States

Background As the population and demand for safe drinking water from domestic wells increase, it is important to examine water quality and contaminant occurrence. A national assessment in 2006 by the U.S. Geological Survey reported findings for 55 volatile organic compounds (VOCs) based on 2,401 domestic wells sampled during 1985–2002. Objectives We examined the occurrence of individual and multiple VOCs and assessed the potential human-health relevance of VOC concentrations. We also identified hydrogeologic and anthropogenic variables that influence the probability of VOC occurrence. Methods The domestic well samples were collected at the wellhead before treatment of water and analyzed for 55 VOCs. Results were used to examine VOC occurrence and identify associations of multiple explanatory variables using logistic regression analyses. We used a screening-level assessment to compare VOC concentrations to U.S. Environmental Protection Agency maximum contaminant levels (MCLs) and health-based screening levels. Results We detected VOCs in 65% of the samples; about one-half of these samples contained VOC mixtures. Frequently detected VOCs included chloroform, toluene, 1,2,4-trimethylbenzene, and perchloroethene. VOC concentrations generally were < 1 μg/L. One or more VOC concentrations were greater than MCLs in 1.2% of samples, including dibromochloropropane, 1,2-dichloropropane, and ethylene dibromide (fumigants); perchloroethene and trichloroethene (solvents); and 1,1-dichloroethene (organic synthesis compound). Conclusions Drinking water supplied by domestic wells is vulnerable to low-level VOC contamination. About 1% of samples had concentrations of potential human-health concern. Identifying factors associated with VOC occurrence may aid in understanding the sources, transport, and fate of VOCs in groundwater.

Environmental Health Perspectives

Occurrence of MTBE and other gasoline oxygenates in CWS source waters

Results from two national surveys indicate that the gasoline oxygenate methyl tertiary butyl ether (MTBE) is one of the most frequently detected volatile organic compounds in source waters used by community water systems in the United States. Three other ether oxygenates were detected infrequently but almost always co-occurred with MTBE. A random sampling of source waters across the United States found MTBE in almost 9% of samples. In geographic areas with high MTBE use, the compound was detected in 23% of source water samples. Although MTBE concentrations were low (<1 µg/L) in most samples, some concentrations equaled or exceeded the drinking water advisory of 20 µg/L set by the US Environmental Protection Agency. The frequent detection of even low concentrations of MTBE demonstrates the vulnerability of US source waters to anthropogenic compounds, indicating a need to include MTBE in monitoring programs to track the trend of contamination.

Journal - American Water Works Association

Volatile organic compounds in the nation's ground water and drinking-water supply wells

This national assessment of 55 volatile organic compounds (VOCs) in ground water gives emphasis to the occurrence of VOCs in aquifers that are used as an important supply of drinking water. In contrast to the monitoring of VOC contamination of ground water at point-source release sites, such as landfills and leaking underground storage tanks (LUSTs), our investigations of aquifers are designed as large-scale resource assessments that provide a general characterization of water-quality conditions. Nearly all of the aquifers included in this assessment have been identified as regionally extensive aquifers or aquifer systems. The assessment of ground water (Chapter 3) included analyses of about 3,500 water samples collected during 1985-2001 from various types of wells, representing almost 100 different aquifer studies. This is the first national assessment of the occurrence of a large number of VOCs with different uses, and the assessment addresses key questions about VOCs in aquifers. The assessment also provides a foundation for subsequent decadal assessments of the U.S. Geological Survey (USGS) National Water-Quality Assessment (NAWQA) Program to ascertain long-term trends of VOC occurrence in these aquifers.

Circular

Approach to an assessment of volatile organic compounds in the nation's ground water and drinking-water supply wells

The National Water-Quality Assessment (NAWQA) Program of the U.S. Geological Survey (USGS) developed an approach for a national assessment of the occurrence, status, and distribution of volatile organic compounds (VOCs) in samples of ground water from aquifer studies and in samples from drinking-water supply wells, specifically domestic and public wells. Data on VOCs in samples from aquifers and from domestic and public wells had three sources: (1) NAWQA sampling of ground water in aquifer studies and of shallow ground water in areas of agricultural or urban land use from 1993-2002, (2) retrospective data from other Federal, State, and local agencies that sampled ground water in aquifer studies from 1985-1997, and (3) sampling of ground water from public wells used as a source of drinking water from 1999-2000 (source-water survey). Data for assessing VOCs in ground water came from the NAWQA sampling of aquifers and from retrospective data (1 and 2). Domestic wells were the most commonly sampled well type in these aquifer studies. Data for assessing VOCs in domestic well samples came from the NAWQA sampling of aquifers and shallow ground water and from retrospective data (1 and 2). Data for assessing VOCs in public well samples came from NAWQA sampling of aquifers and shallow ground water and from the source-water survey (1, 2, and 3). Fifty-five VOCs were included in the national assessment. All ground-water samples were collected using consistent, prescribed field protocols and were analyzed using approved analytical methods. All ground-water collection activities and laboratory procedures included the collection of various quality-control samples in order to ensure the quality of the data. Comparisons of detection frequencies and detected concentrations among individual VOCs, groups of VOCs, aquifer studies, and data sets were performed using two assessment levels: (1) an assessment level of 0.2 microgram per liter (?g/L), and (2) an assessment level of 0.02 ?g/L. Selection of the 0.2-?g/L assessment level was based on historical laboratory reporting levels of VOCs used by the USGS National Water-Quality Laboratory (NWQL) prior to April 1996, and selection of the 0.02-?g/L assessment level was based on a new, low-level analytical method developed by the NWQL and used since April 1996. Relational analyses using multivariate logistic regression were performed on VOC data from aquifers, domestic wells, and public wells to better understand the natural and anthropogenic factors that control or influence the occurrence of VOCs. Ancillary data used in the relational analyses represent a variety of anthropogenic and hydrogeologic controls on the occurrence of VOCs. For aquifers, relational analyses were performed only on NAWQA data analyzed using the new low-level analytical method for 10 frequently detected VOCs. For domestic wells, relational analyses were performed at assessment levels of 0.2 ?g/L and 0.02 ?g/L for 6 and 10 frequently detected VOCs at these levels. For public wells, relational analyses were performed at an assessment level of 0.2 ?g/L for nine frequently detected VOCs.

Open-File Report

The occurrence of volatile organic compounds in aquifers of the United States

The U.S. Geological Survey's National Water-Quality Assessment (NAWQA) Program recently completed a national assessment of volatile organic compounds (VOCs) in ground water (Zogorski and others, 2006). As part of this assessment, samples of ambient ground water collected from 3,498 wells during 1985-2002 were selected for characterizing the occurrence of 55 VOCs in 98 aquifer studies. The 55 VOCs were assigned to the following groups on the basis of their primary usage (or origin): (1) fumigants, (2) gasoline hydrocarbons, (3) gasoline oxygenates, (4) organic synthesis compounds, (5) refrigerants, (6) solvents, and (7) trihalo-methanes (chlorination by-products). The samples were collected throughout the conterminous United States as well as Alaska and Hawaii. The sampled wells had a variety of uses including domestic supply (61 percent), public supply (15 percent), monitoring (10 percent), other (13 percent), and unknown (1 percent). NAWQA aquifer studies are large-scale resource assessments of ground water that provide a general characterization of water-quality conditions in locally and regionally important aquifers or portions thereof. In general, the aquifers (or portions thereof) selected for study were some of the most intensively used aquifers for drinking water in greaterHawaiiOahuAlaskathe Nation. The 98 aquifer studies collectively provide an important national perspective on the current (1985-2002) extent of VOC contamination and regional patterns of VOC occurrence in ground water. More information about this national assessment of VOCs is available at a supporting Web site (http://water.usgs.gov/nawqa/vocs/national_assessment).

Scientific Investigations Map

Volatile organic compounds in samples from domestic and public wells, 1985-2002

The U.S. Geological Survey's (USGS) National Water-Quality Assessment (NAWQA) Program recently completed a national study of volatile organic compounds (VOCs) in the Nation's ground water (Zogorski and others, 2006). Part of this assessment emphasizes the occurrence of 55 VOCs in samples from 2,401 domestic wells and 1,096 public wells during 1985-2002. Samples were collected prior to any treatment or blending of water. Domestic wells are privately owned, self-supplied sources used for drinking water and household use (Moran and others, 2002). Public wells are privately or publicly owned and supply water to public water systems (PWSs). Samples from public wells in this assessment characterize the quality of water captured by wells that supply drinking water to PWSs. These systems supply drinking water to at least 15 service connections or regularly serve at least 25 individuals daily at least 60 days a year (U.S. Environmental Protection Agency, 2005). For a screening-level assessment, VOC concentrations were compared to human-health benchmarks. Concentrations greater than the U.S. Environmental Protection Agency's (USEPA) Maximum Contamination Levels (MCLs) (U.S. Environmental Protection Agency, 2004) or the USGS's Health-Based Screening Levels (HBSLs) (Zogorski and others, 2006) were considered of potential human-health concern. The findings from the well samples provide an important perspective on the quality of the Nation's ground water used for drinking-water supplies. More information about this national assessment of VOCs is available (http://water.usgs.gov/nawqa/vocs/national_assessment).

Scientific Investigations Map

Occurrence of trihalomethanes in the nation's ground water and drinking-water supply wells, 1985-2002

This report describes the occurrence of trihalomethanes (THMs) in the Nation's ground water and drinking-water supply wells based on analysis of 5,642 samples of untreated ground water and source water collected or compiled during 1985-2002 by the U.S. Geological Survey National Water-Quality Assessment (NAWQA) Program. THMs are a group of volatile organic compounds (VOCs) with natural and anthropogenic sources that are of interest because they are associated with acute and chronic health problems in humans. THMs occur in water primarily from chlorination and are classified as disinfection by-products. In this report, the four THMs are discussed in the order of chloroform, bromodichloromethane, dibromochloromethane, and then bromoform; this sequence corresponds to largest to smallest chlorine content and smallest to largest bromine content. Four trihalomethanes were detected in less than 20 percent of samples from studies of (1) aquifers, (2) shallow ground water in agricultural areas, (3) shallow ground water in urban areas, (4) domestic wells, and (5) public wells. Detection frequencies for individual THMs in the five studies ranged from zero for shallow ground water in agricultural areas to 19.5 percent for shallow ground water in urban areas. None of the samples from aquifer studies, domestic wells, or public wells had total THM concentrations (the sum of the concentrations of chloroform, bromodichloromethane, dibromochloromethane, and bromoform) greater than or equal to the U.S. Environmental Protection Agency Maximum Contaminant Level of 80 micrograms per liter (?g/L). Comparisons of results among studies of aquifers, shallow ground water in agricultural areas, and shallow ground water in urban areas were used to describe the occurrence of the four THMs in ground water for three different land-use settings-mixed, agricultural, and urban, respectively. At the 0.2-?g/L assessment level, one or more of the four THMs were detected in 7.9 percent of the samples from aquifer studies, 2.2 percent of the samples from shallow ground water in agricultural areas, and 19.5 percent of the samples from shallow ground water in urban areas. In general, detection frequencies and concentrations of the four THMs were greater in shallow ground water in urban areas compared to aquifer studies and to shallow ground water in agricultural areas. For all three of these studies, the most common two-THM mixture at the 0.2-?g/L assessment level was chloroform-bromodichloromethane, and this was the only two-THM mixture found in samples of shallow ground water in agricultural areas. Comparisons of results between studies of domestic wells and public wells were used to describe the occurrence of the four THMs in two different supplies of ground water used for drinking water. At the 0.2-?g/L assessment level, one or more of the four THMs were detected in 5.2 percent of the domestic well samples and in 14.7 percent of the public well samples. In general, detection frequencies and THM concentrations were greater in samples from public wells than from domestic wells. At the 0.2-?g/L assessment level, the six possible two-THM mixtures occurred about six times more frequently in samples from public wells than from domestic wells. One of the most common two-THM mixtures in samples from domestic and public wells was bromodichloromethane-dibromochloromethane. Detection frequency is associated with the chlorine content of the THM compound. In general, for each of the five studies, as the chlorine content of the THM compound decreased, the detection frequency at the 0.2-?g/L assessment level also decreased. The exception was the study of public wells in which the detection frequency of the THMs decreased in the following order: chloroform, bromoform, dibromochloromethane, and bromodichloromethane. At the 0.2-?g/L assessment level, the median concentration for one or more of the four THMs ranged from 0.3 ?g/L (shallow ground water in agricultural a

Scientific Investigations Report

StreamVOC - A deterministic source-apportionment model to estimate volatile organic compound concentrations in rivers and streams

This report documents the construction and verification of the model, StreamVOC, that estimates (1) the time- and position-dependent concentrations of volatile organic compounds (VOCs) in rivers and streams as well as (2) the source apportionment (SA) of those concentrations. The model considers how different types of sources and loss processes can act together to yield a given observed VOC concentration. Reasons for interest in the relative and absolute contributions of different sources to contaminant concentrations include the need to apportion: (1) the origins for an observed contamination, and (2) the associated human and ecosystem risks. For VOCs, sources of interest include the atmosphere (by absorption), as well as point and nonpoint inflows of VOC-containing water. Loss processes of interest include volatilization to the atmosphere, degradation, and outflows of VOC-containing water from the stream to local ground water. This report presents the details of StreamVOC and compares model output with measured concentrations for eight VOCs found in the Aberjona River at Winchester, Massachusetts. Input data for the model were obtained during a synoptic study of the stream system conducted July 11-13, 2001, as part of the National Water-Quality Assessment (NAWQA) Program of the U.S. Geological Survey. The input data included a variety of basic stream characteristics (for example, flows, temperature, and VOC concentrations). The StreamVOC concentration results agreed moderately well with the measured concentration data for several VOCs and provided compound-dependent SA estimates as a function of longitudinal distance down the river. For many VOCs, the quality of the agreement between the model-simulated and measured concentrations could be improved by simple adjustments of the model input parameters. In general, this study illustrated: (1) the considerable difficulty of quantifying correctly the locations and magnitudes of ground-water-related sources of contamination in streams; and (2) that model-based estimates of stream VOC concentrations are likely to be most accurate when the major sources are point sources or tributaries where the spatial extent and magnitude of the sources are tightly constrained and easily determined.

Scientific Investigations Report

Health-Based Screening Levels and their Application to Water-Quality Data

To supplement existing Federal drinking-water standards and guidelines, thereby providing a basis for a more comprehensive evaluation of contaminant-occurrence data in a human-health context, USGS began a collaborative project in 1998 with USEPA, the New Jersey Department of Environmental Protection, and the Oregon Health & Science University to calculate non-enforceable health-based screening levels. Screening levels were calculated for contaminants that do not have Maximum Contaminant Level values using a consensus approach that entailed (1) standard USEPA Office of Water methodologies (equations) for establishing Lifetime Health Advisory (LHA) and Risk-Specific Dose (RSD) values for the protection of human health, and (2) existing USEPA human-health toxicity information.

Fact Sheet