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USGS2008

Assessment of Water-Quality Conditions in Fivemile Creek in the Vicinity of the Fivemile Creek Greenway, Jefferson County, Alabama, 2003-2005

The watershed of Fivemile Creek (FMC), a tributary to the Locust Fork of the Black Warrior River, is located north of Birmingham, Alabama. Areas that have been previously coal-mined border the creek, and portions of the upper watershed have been and are currently (2007) being used for industrial and urban uses. The U.S. Geological Survey (USGS), in cooperation with the City of Tarrant, the Freshwater Land Trust, and the Jefferson County Commission, conducted a water-quality assessment of 12 sites along FMC during 2003?2005. Water samples were analyzed for basic physical and chemical properties and concentrations of major ions, nutrients, fecal indicator bacteria, organic wastewater compounds, pesticides, trace elements, and semivolatile organic compounds. Streambed-sediment samples were analyzed for concentrations of trace elements and semivolatile organic compounds. Benthic invertebrate communities were evaluated for taxonomic composition and relation to water-quality conditions. Nutrient concentrations in the FMC watershed reflect the influences of natural and anthropogenic sources. Concentrations of total nitrogen in all samples and total Kjeldahl nitrogen in at least one sample each collected from FMC at Hewitt Park, FMC below Springdale Road, FMC at Lewisburg, FMC near Republic, FMC at Brookside, and FMC at Linn Crossing exceeded U.S. Environmental Protection Agency (USEPA) ecoregion nutrient criteria. Total phosphorus concentrations in about 58 percent of all samples were above the ecoregion nutrient criteria. Concentrations of chlorophyll a, an indicator of algal biomass, in the FMC watershed were below the appropriate USEPA ecoregion criteria. Fecal indicator bacteria concentrations occasionally exceeded criteria established by the Alabama Department of Environmental Management (ADEM) and the USEPA to protect human health and aquatic life. Median fecal-coliform concentrations equaled or exceeded USEPA criteria at four of the six sites with multiple samples. Maximum Escherichia coli (E. coli) concentrations usually occurred during high-flow conditions and exceeded the single-sample criterion for infrequently-used whole-body contact (576 colonies per 100 milliliters) at all but one site. Median E. coli concentrations for two of the seven sites with multiple samples exceeded USEPA criteria. Twenty-nine samples were collected from sites along FMC and analyzed by the USGS National Water Quality Laboratory for the presence of 57 organic wastewater compounds. Forty-six of the 57 organic wastewater compounds, representing all 11 general-use categories, were detected in samples from FMC. All detections of organic wastewater compounds were estimated below laboratory reporting limits except for several detections of the herbicide bromacil. Herbicides accounted for approximately 62 percent of the number of pesticide detections in the FMC study area. Two herbicides, atrazine and simazine, were detected most frequently, in 100 percent of the surface-water samples. Fipronil sulfide was the most commonly detected insecticide-derived compound, occurring in 52 percent of the surface-water samples. Concentrations of one insecticide, dieldrin, exceeded the USEPA?s health advisory level for drinking water in one sample at FMC at Hewitt Park and in one sample at FMC below Springdale Road. Concentrations of carbaryl in two samples and malathion in one sample exceeded aquatic-life criteria. Only a few trace element concentrations measured in FMC exceeded established standards or criteria. Some concentrations of aluminum and manganese were above secondary drinking-water standards. One cadmium concentration and three selenium concentrations measured at FMC at Lewisburg exceeded ADEM chronic aquatic-life criteria. Streambed-sediment samples were collected at seven sites along FMC, and analyzed for selected semivolatile organic compounds and trace elements. Forty-nine of 98 semivolatile organic compounds were detected in stre

Scientific Investigations Report↗

USGS2010

Quality of Source Water from Public-Supply Wells in the United States, 1993-2007

More than one-third of the Nation's population receives their drinking water from public water systems that use groundwater as their source. The U.S. Geological Survey (USGS) sampled untreated source water from 932 public-supply wells, hereafter referred to as public wells, as part of multiple groundwater assessments conducted across the Nation during 1993-2007. The objectives of this study were to evaluate (1) contaminant occurrence in source water from public wells and the potential significance of contaminant concentrations to human health, (2) national and regional distributions of groundwater quality, and (3) the occurrence and characteristics of contaminant mixtures. Treated finished water was not sampled. The 932 public wells are widely distributed nationally and include wells in selected parts of 41 states and withdraw water from parts of 30 regionally extensive aquifers used for public water supply. These wells are distributed among 629 unique public water systems-less than 1 percent of all groundwater-supplied public water systems in the United States-but the wells were randomly selected within the sampled hydrogeologic settings to represent typical aquifer conditions. Samples from the 629 systems represent source water used by one-quarter of the U.S. population served by groundwater-supplied public water systems, or about 9 percent of the entire U.S. population in 2008. One groundwater sample was collected prior to treatment or blending from each of the 932 public wells and analyzed for as many as six water-quality properties and 215 contaminants. Consistent with the terminology used in the Safe Drinking Water Act (SDWA), all constituents analyzed in water samples in this study are referred to as 'contaminants'. More contaminant groups were assessed in this study than in any previous national study of public wells and included major ions, nutrients, radionuclides, trace elements, pesticide compounds, volatile organic compounds (VOCs), and fecal-indicator microorganisms. Contaminant mixtures were assessed in subsets of samples in which most contaminants were analyzed. Contaminant concentrations were compared to human-health benchmarks-regulatory U.S. Environmental Protection Agency (USEPA) Maximum Contaminant Levels (MCLs) for contaminants regulated in drinking water under the SDWA or non-regulatory USGS Health-Based Screening Levels (HBSLs) for unregulated contaminants, when available. Nearly three-quarters of the contaminants assessed in this study are unregulated in drinking water, and the USEPA uses USGS data on the occurrence of unregulated contaminants in water resources to fulfill part of the SDWA requirements for determining whether specific contaminants should be regulated in drinking water in the future. More than one in five (22 percent) source-water samples from public wells contained one or more naturally occurring or man-made contaminants at concentrations greater than human-health benchmarks, and 80 percent of samples contained one or more contaminants at concentrations greater than one-tenth of benchmarks. Most individual contaminant detections, however, were less than one-tenth of human-health benchmarks. Public wells yielding water with contaminant concentrations greater than benchmarks, as well as those with concentrations greater than one-tenth of benchmarks, were distributed throughout the United States and included wells that withdraw water from all principal aquifer rock types included in this study. Ten contaminants individually were detected at concentrations greater than human-health benchmarks in at least 1 percent of source-water samples and collectively accounted for most concentrations greater than benchmarks. Seven of these 10 contaminants occur naturally, including three radionuclides (radon, radium, and gross alpha-particle radioactivity) and four trace elements (arsenic, manganese, strontium, and boron); three of these 10 contaminants (dieldrin, nitrate, and perchl

Scientific Investigations Report↗

USGS1951

Airborne radioactivity survey in the vicinity of Grants, McKinley and Valencia Counties, New Mexico

An airborne radioactivity survey in the vicinity of Grants, New Mexico, was made on May 28. 1951; aeromagnetic measurements were made concurrently with the radioactivity measurements. Several radioactivity anomalies were noted in conjunction with negative magnetic anomalies; this association is unusual and may reflect a genetic relationship between the uranium mineralization and the geologic structure causing the negative magnetic effect. Further investigation of the vicinity of the anomalies near the Haystack area, including ground magnetometer survey, seems warranted.

New Mexico↗

USGS1984

Reconnaissance of water-quality characteristics of streams in the City of Charlotte and Mecklenburg County, North Carolina

In 1979-81, water samples were collected from 119 sites on streams throughout the City of Charlotte and Mecklenburg County, North Carolina, and were analyzed for specific conductance, dissolved chloride, hardness, pH, total alkalinity, total phosphorus, trace elements, arsenic, cadmium, chromium, copper, iron, lead, manganese, mercury, silver, and zinc and biological measures including dissolved oxygen, biochemical oxygen demand, fecal coliform bacteria, and fecal streptococcus bacteria. Sampling was conducted during both low flow (base flow) and high flow. Several water-quality measures including pH, total arsenic, total cadmium, total chromium, total copper, total iron, total lead, total manganese, total mercury, total silver, total zinc, dissolved oxygen, and fecal coliform bacteria at times exceeded North Carolina water-quality standards in various streams. Runoff from non-point sources appears to contribute more to the deterioration of streams in Charlotte and Mecklenburg County than point-source effluents. Urban and industrial areas contribute various trace elements. Residential and rural areas and municipal waste-water treatment plants contribute high amounts of phosphorus.

North Carolina↗

USGS1999

Hydrogeology and water quality of the Nutmeg Valley area, Wolcott and Waterbury, Connecticut

Hydrogeologic investigations in an industrial area in Wolcott and Waterbury, Connecticut, have provided information on the geology, ground-water flow, and water quality of the area. Ground-water contamination by volatile organic compounds was discovered in the 1980?s in the Nutmeg Valley area, where approximately 43 industries and 25 residences use ground water for industrial and domestic supply. Unconsolidated surficial deposits, including glacial stratified deposits and till, are more than 85 feet thick and are interconnected with the underlying bedrock. The horizontal hydraulic conductivity of the stratified deposits ranges from 0.8 to 21 feet per day. Water in the surficial aquifer generally flows toward discharge points along Old Tannery Brook and the Mad River. Water in the bedrock aquifer flows through low-angle unroofing joints, high-angle fractures, and foliation-parallel fractures. Most high-angle water-bearing fractures strike north with an easterly dip. Most of the water pumped from bedrock wells in the study area comes from shallow fractures that are probably in hydraulic connection with the surficial aquifer. Short-circuit flow between fracture zones in wells is a likely pathway for contaminant transport. During periods of low streamflow, only a small amount of ground water discharges directly to Old Tannery Brook or to the Mad River. The amount of discharge is on the same order of magnitude as the estimated ground-water withdrawals. In northern parts of the valley bottom within the study area, downward vertical hydraulic gradients were present between wells in the surficial and bedrock aquifers. In southern parts of the valley, however, vertical gradients were upward from the bedrock to the surficial aquifer. Vertical gradients can change seasonally in response to different amounts of ground-water recharge and to stresses caused by ground-water withdrawals, which can in turn facilitate the spread of contamination. Vapor-diffusion samplers were installed in streambeds to identify zones where water containing volatile organic compounds was discharging to streams in the study area. Three areas with high vapor concentrations of trichloroethene and tetrachloroethene were identified. Concentrations of trichloroethene as high as 30,000 parts per billion by volume were detected. Three of 44 wells sampled contained concentrations of volatile organic compounds, including trichloroethene and tetrachloroethene, above primary drinking water standards. Based on the findings of this and previous investigations, water in the bedrock aquifer in the southern part of the study area is likely to contain trichloroethene, tetrachloroethene, and 1,1,1-trichloroethane. Volatile organic compounds also were detected in stream samples from the downstream end of Old Tannery Brook and the Mad River. Concentrations of major ions and trace elements (with one exception) did not exceed primary drinking water standards in any ground-water or surface-water samples collected. Ground-water samples collected downgradient from the Waterbury North End Disposal Area contained ethyl ether, chlorobenzene, and elevated concentrations of dissolved solids, similar to samples of landfill leachate and groundwater samples collected from springs and wells adjacent to the landfill.

Water-Resources Investigations Report↗

USGS1989

Present-day biogeochemical activities of anaerobic bacteria and their relevance to future exobiological investigations

If the primordial atmosphere was reducing, then the first microbial ecosystem was probably composed of anaerobic bacteria. However, despite the presence of an oxygen-rich atmosphere, anaerobic habitats are important, commonplace components of the Earth's present biosphere. The geochemical activities displayed by these anaerobes impact the global cycling of certain elements (e.g., C, N, S, Fe, Mn, etc.). Methane provides an obvious example of how human-enhanced activities on a global scale can influence the content of a "radiative" (i.e., infrared absorbing) trace gas in the atmosphere. Methane can be oxidized by anaerobic bacteria, but this does not appear to support their growth. Acetylene, however, does support such growth. This may form the basis for future exobiological investigations of the atmospheres of anoxic, hydrocarbon-rich planets like Jupiter and Saturn, as well as the latter's satellite Titan.

Advances in Space Research↗

USGS2011

Trace elements and radon in groundwater across the United States, 1992-2003

Trace-element concentrations in groundwater were evaluated for samples collected between 1992 and 2003 from aquifers across the United States as part of the U.S. Geological Survey National Water-Quality Assessment Program. This study describes the first comprehensive analysis of those data by assessing occurrence (concentrations above analytical reporting levels) and by comparing concentrations to human-health benchmarks (HHBs). Data from 5,183 monitoring and drinking-water wells representing more than 40 principal and other aquifers in humid and dry regions and in various land-use settings were used in the analysis. Trace elements measured include aluminum (Al), antimony (Sb), arsenic (As), barium (Ba), beryllium (Be), boron (B), cadmium (Cd), chromium (Cr), cobalt (Co), copper (Cu), iron (Fe), lead (Pb), lithium (Li), manganese (Mn), molybdenum (Mo), nickel (Ni), selenium (Se), silver (Ag), strontium (Sr), thallium (Tl), uranium (U), vanadium (V), and zinc (Zn). Radon (Rn) gas also was measured and is included in the data analysis. Climate influenced the occurrence and distribution of trace elements in groundwater whereby more trace elements occurred and were found at greater concentrations in wells in drier regions of the United States than in humid regions. In particular, the concentrations of As, Ba, B, Cr, Cu, Mo, Ni, Se, Sr, U, V, and Zn were greater in the drier regions, where processes such as chemical evolution, ion complexation, evaporative concentration, and redox (oxidation-reduction) controls act to varying degrees to mobilize these elements. Al, Co, Fe, Pb, and Mn concentrations in groundwater were greater in humid regions of the United States than in dry regions, partly in response to lower groundwater pH and (or) more frequent anoxic conditions. In groundwater from humid regions, concentrations of Cu, Pb, Rn, and Zn were significantly greater in drinking-water wells than in monitoring wells. Samples from drinking-water wells in dry regions had greater concentrations of As, Ba, Pb, Li, Sr, V, and Zn, than samples from monitoring wells. In humid regions, however, concentrations of most trace elements were greater in monitoring wells than in drinking-water wells; the exceptions were Cu, Pb, Zn, and Rn. Cu, Pb, and Zn are common trace elements in pumps and pipes used in the construction of drinking-water wells, and contamination from these sources may have contributed to their concentrations. Al, Sb, Ba, B, Cr, Co, Fe, Mn, Mo, Ni, Se, Sr, and U concentrations were all greater in monitoring wells than in drinking-water wells in humid regions. Groundwater from wells in agricultural settings had greater concentrations of As, Mo, and U than groundwater from wells in urban settings, possibly owing to greater pH in the agricultural wells. Significantly greater concentrations of B, Cr, Se, Ag, Sr, and V also were found in agricultural wells in dry regions. Groundwater from dry-region urban wells had greater concentrations of Co, Fe, Pb, Li, Mn, and specific conductance than groundwater from agricultural wells. The geologic composition of aquifers and aquifer geochemistry are among the major factors affecting trace-element occurrence. Trace-element concentrations in groundwater were characterized in aquifers from eight major groups based on geologic material, including (1) unconsolidated sand and gravel; (2) glacial unconsolidated sand and gravel; (3) semiconsolidated sand; (4) sandstone; (5) sandstone and carbonate rock; (6) carbonate rock; (7) basaltic and other volcanic rock; and (8) crystalline rock. The majority of groundwater samples and the largest percentages of exceedences of HHBs were in the glacial and nonglacial unconsolidated sand and gravel aquifers; in these aquifers, As, Mn, and U are the most common trace elements exceeding HHBs. Overall, 19 percent of wells (962 of 5,097) exceeded an HHB for at least one trace element. The trace elements with HHBs included in this summary were Sb, As, Ba, Be, B, Cd, Cr,

Scientific Investigations Report↗

USGS2016

Capsule- and disk-filter procedure

Capsule and disk filters are disposable, self-contained units composed of a pleated or woven filter medium encased in a polypropylene or other plastic housing that can be connected inline to a sample-delivery system (such as a submersible or peristaltic pump) that generates sufficient pressure (positive or negative) to force water through the filter. Filter media are available in several pore sizes, but 0.45 µm is the pore size used routinely for most studies at this time. Capsule or disk filters (table 5.2.1.A.1) are required routinely for most studies when filtering samples for trace-element analyses and are recommended when filtering samples for major-ion or other inorganic-constituent analyses.

Techniques of Water-Resources Investigations↗

USGS1998

Water-quality trends in the Santa Ana River at MWD Crossing and below Prado Dam, Riverside County, California

The Santa Ana River, located in an extensively urbanized basin, drains about 2,670 square miles near Los Angeles, California. Almost all flow in the river, about 200,000 acre-feet annually, is diverted to ponds where it infiltrates and recharges underlying aquifers. About 2 million people are dependent on these aquifers for water supply. In recent years, base flow in the river has increased as a result of increased discharge of treated municipal wastewater, and high flows have increased as a result of increase precipitation and urbanization. Trends in water quality were calculated for two sites?at the Metropolitan Water District (MWD) Crossing (an upstream site) and below Prado Dam (a downstream site)?using the computer program ESTREND. Water-quality data for these sites were collected by the U.S. Geological Survey from 1969 to 1995. At MWD Crossing, flow-adjusted downward trends of -1.1 microsiemens per centimeter (iS/cm) per year and -1.6 milligrams per liter (mg/L) per year were calculated for specific conductance and dissolved solids, respectively. In contrast, a flow-adjusted upward trends of 2.2 iS/cm per year for dissolved solids was calculated for the Santa Ana River below Prado Dam. Specific conductance and dissolved solids in the Santa Ana River below Prado Dam had downward unadjusted trends (not adjusted for streamflow) of -8.3 iS/cm per year and -6.0 mg/L per year, respectively. For the Santa Ana River below Prado Dam, downward unadjusted trends were calculated for ammonia (-0.04 mg/L per year) and total organic carbon (0.19 mg/L per year); flow-adjusted upward trends were calculated for nitrite plus nitrate (0.15 mg/L per year), total dissolved nitrogen (0.39 mg/L per year), and orthophosphate (0.03 mg/L per year). Statistically significant unadjusted and flow-adjusted trends were not obtained for organic nitrogen, phosphorus, and dissolved organic carbon. Data for selected trace elements and organic compounds collected between 1970-94 also are summarized in this report.

Water-Resources Investigations Report↗

USGS2002

Stability of dilute solutions of uranium, lead, and thorium ions

Standard solutions and samples containing a few micrograms of metallic ions per milliliter are frequently used in determination of trace elements. It is important to know whether the concentrations of such solutions remain constant from day to day. The stability of dilute solutions of three metallic ions-uranium, lead, and thorium-has been investigated. Solutions containing concentrations of metallic ions, ranging from 1000 to 0.1 γ per milliliter, were allowed to stand for approximately 2.5 months, and then the metallic ion content of those solutions that had lost strength was determined. Both adsorption and hydrolysis variously influenced the solute loss, but the minimum pH at which loss of concentration of lead and uranium occurred seemed to coincide with the pH at which the hydrolyzed metal ions began to precipitate. No increase in the stability of the solutions was obtained by substituting polyethylene containers for borosilicate glass. The solutions that lost strength could not be restored promptly to the original concentration by manual means, such as shaking them vigorously for several minutes.

Analytical Chemistry↗

USGS1956

Radiometric investigations along the Taylor Highway and part of the Tanana River, Alaska

No abstract available.

Alaska↗

USGS1988

Reconnaissance investigation of water quality, bottom sediment, and biota associated with irrigation drainage in the Kendrick Reclamation Project Area, Wyoming, 1986-87

A reconnaissance investigation of the Kendrick Reclamation Project in central Wyoming was conducted during 1986-87 to determine if irrigation drainage has caused or has the potential to cause harmful effects on human health, fish, and wildlife, or other water uses. The investigation of the Kendrick Reclamation Project is one of nine similar investigations being conducted in the western conterminous United States as part of the Department of the Interior 's Irrigation Drainage Program. Samples of surface water were collected at 10 sites and ground water at 5 sites. Surface-water analyses included trace elements, radiochemicals, and pesticides. Concentrations in the water generally were less than national standards for public water supplies, with the exception of selenium. The median concentration of dissolved selenium was 7.5 microgm/L in 24 samples of surface and groundwater. Of the 11 samples that contained dissolved- selenium concentrations greater than the national standard for public water supplies of 10 microgm/L, 10 of the samples were collected at sites on streams that are not used for public water supplies; the eleventh sample was collected from a shallow well. Dissolved-selenium concentrations ranged from less than 1 to 300 microgm/L. Concentrations of dissolved selenium in the North Platte River, which supplies drinking water for several municipalities, ranged from less than 1 to 4 microgm/L. The dissolved-selenium concentration and selenium discharge in the North Platte River increased in the downstream direction. The four principal tributaries that receive drainage from the Kendrick Reclamation Project contributed substantially to the increase in selenium concentration and discharge in the North Platte River. Bottom-sediment samples from the North Platte River contained selenium contents of 1.2 microgm/g or less. (Author 's abstract)

Water-Resources Investigations Report↗

USGS2009

Groundwater quality data for the Tahoe-Martis study unit, 2007: Results from the California GAMA Program

Groundwater quality in the approximately 460-square-mile Tahoe–Martis study unit was investigated in June through September 2007 as part of the Priority Basin Project of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The GAMA Priority Basin Project was developed in response to the Groundwater Quality Monitoring Act of 2001 and is being conducted by the U.S. Geological Survey (USGS) in cooperation with the California State Water Resources Control Board (SWRCB). The study was designed to provide a spatially unbiased assessment of the quality of raw groundwater used for public water supplies within the Tahoe–Martis study unit (Tahoe–Martis) and to facilitate statistically consistent comparisons of groundwater quality throughout California. Samples were collected from 52 wells in El Dorado, Placer, and Nevada Counties. Forty-one of the wells were selected using a spatially distributed, randomized grid-based method to provide statistical representation of the study area (grid wells), and 11 were selected to aid in evaluation of specific water-quality issues (understanding wells). The groundwater samples were analyzed for a large number of synthetic organic constituents (volatile organic compounds [VOC], pesticides and pesticide degradates, and pharmaceutical compounds), constituents of special interest (perchlorate and N -nitrosodimethylamine [NDMA]), naturally occurring inorganic constituents (nutrients, major and minor ions, and trace elements), radioactive constituents, and microbial indicators. Naturally occurring isotopes (tritium, carbon-14, strontium isotope ratio, and stable isotopes of hydrogen and oxygen of water), and dissolved noble gases also were measured to help identify the sources and ages of the sampled groundwater. In total, 240 constituents and water-quality indicators were investigated. Three types of quality-control samples (blanks, replicates, and samples for matrix spikes) each were collected at 12 percent of the wells, and the results obtained from these samples were used to evaluate the quality of the data for the groundwater samples. Field blanks rarely contained detectable concentrations of any constituent, suggesting that data for the groundwater samples were not compromised by possible contamination during sample collection, handling or analysis. Differences between replicate samples were within acceptable ranges. Matrix spike recoveries were within acceptable ranges for most compounds. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, raw water typically is treated, disinfected, or blended with other waters to maintain water quality. Regulatory thresholds apply to water that is served to the consumer, not to raw groundwater. However, to provide some context for the results, concentrations of constituents measured in the raw groundwater were compared with regulatory and nonregulatory health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and the California Department of Public Health (CDPH), and with aesthetic and technical thresholds established by CDPH. Comparisons between data collected for this study and drinking-water thresholds are for illustrative purposes only and do not indicate of compliance or noncompliance with regulatory thresholds. The concentrations of most constituents detected in groundwater samples from the Tahoe–Martis wells were below drinking-water thresholds. Organic compounds (VOCs and pesticides) were detected in about 40 percent of the samples from grid wells, and most concentrations were less than 1/100th of regulatory and nonregulatory health-based thresholds, although the conentration of perchloroethene in one sample was above the USEPA maximum contaminant level (MCL-US). Concentrations of all trace elements and nutrients in samples from grid wells were below regulatory and nonregulatory health-based thresholds, with five exceptions. Concentrations of arsenic were above the MCL-US in 20 percent of the samples from grid wells. Gross alpha particle activity (MCL-US), boron (CDPH notification level, NL-CA), and molybdenum (USEPA lifetime health advisory, HAL-US) were each detected above thresholds in two of the samples from grid wells, and radon (proposed alternative MCL-US) was detected above the threshold in one sample from a grid well. Most of the samples from Tahoe–Martis grid wells had concentrations of major elements, total dissolved solids, and trace elements below the CDPH secondary maximum contaminant levels, nonenforceable thresholds set for aesthetic and technical concerns. Fifteen percent of the samples from grid wells contained iron, manganese, or total dissolved solids at concentrations above these levels.

California, Nevada↗

USGS2010

Groundwater-quality data in the Colorado River study unit, 2007: Results from the California GAMA Program

Groundwater quality in the 188-square-mile Colorado River Study unit (COLOR) was investigated October through December 2007 as part of the Priority Basin Project of the California State Water Resources Control Board (SWRCB) Groundwater Ambient Monitoring and Assessment (GAMA) Program. The GAMA Priority Basin Project was developed in response to the Groundwater Quality Monitoring Act of 2001, and the U.S. Geological Survey (USGS) is the technical project lead. The Colorado River study was designed to provide a spatially unbiased assessment of the quality of raw groundwater used for public water supplies within COLOR, and to facilitate statistically consistent comparisons of groundwater quality throughout California. Samples were collected from 28 wells in three study areas in San Bernardino, Riverside, and Imperial Counties. Twenty wells were selected using a spatially distributed, randomized grid-based method to provide statistical representation of the Study unit; these wells are termed ‘grid wells’. Eight additional wells were selected to evaluate specific water-quality issues in the study area; these wells are termed ‘understanding wells.’ The groundwater samples were analyzed for organic constituents (volatile organic compounds [VOC], gasoline oxygenates and degradates, pesticides and pesticide degradates, pharmaceutical compounds), constituents of special interest (perchlorate, 1,4-dioxane, and 1,2,3-trichlorpropane [1,2,3-TCP]), naturally occurring inorganic constituents (nutrients, major and minor ions, and trace elements), and radioactive constituents. Concentrations of naturally occurring isotopes (tritium, carbon-14, and stable isotopes of hydrogen and oxygen in water), and dissolved noble gases also were measured to help identify the sources and ages of the sampled groundwater. In total, approximately 220 constituents and water-quality indicators were investigated. Quality-control samples (blanks, replicates, and matrix spikes) were collected at approximately 30 percent of the wells, and the results were used to evaluate the quality of the data obtained from the groundwater samples. Field blanks rarely contained detectable concentrations of any constituent, suggesting that contamination was not a significant source of bias in the data. Differences between replicate samples were within acceptable ranges and matrix-spike recoveries were within acceptable ranges for most compounds. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, raw groundwater typically is treated, disinfected, or blended with other waters to maintain acceptable water quality. Regulatory thresholds apply to water that is served to the consumer, not to raw groundwater. However, to provide some context for the results, concentrations of constituents measured in the raw groundwater were compared to regulatory and nonregulatory health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and the California Department of Public Health (CDPH) and to thresholds established for aesthetic concerns by CDPH. Comparisons between data collected for this study and drinking-water thresholds are for illustrative purposes only and do not indicate compliance or noncompliance with those thresholds. The concentrations of most constituents detected in groundwater samples were below drinking-water thresholds. Volatile organic compounds (VOC) were detected in approximately 35 percent of grid well samples; all concentrations were below health-based thresholds. Pesticides and pesticide degradates were detected in about 20 percent of all samples; detections were below health-based thresholds. No concentrations of constituents of special interest or nutrients were detected above health-based thresholds. Most of the major and minor ion constituents sampled do not have health-based thresholds; the exception is chloride. Concentrations of chloride, sulfate, and total dissolved solids detected in some of the well samples were above the nonenforceable thresholds for aesthetic concerns. Concentrations of fluoride were detected in 5 samples (from 4 grid wells and 1 understanding well) above the maximum contaminant level for California (MCL-CA). Concentrations of most of the trace elements in samples from the COLOR study were below health-based thresholds; exceptions included arsenic above the MCL-US, boron above the notification level for California (NL-CA), iron and manganese above the secondary maximum contaminant level for California (SMCL-CA), and molybdenum and strontium above the lifetime health advisory level (HAL-US) threshold. Most detections of radioactive constituents were below health-based thresholds; exceptions were alpha, uranium, and radon radioactivity. Alpha radioactivity with 72 hour count detections occurred in four grid wells and one understanding well, and 30-day count detections in two grid wells above the MCL-US. Uranium was detected twice in grid wells above the MCL-US threshold. Also, radon-222 was detected at concentrations above the proposed MCL-US in 19 samples (14 grid and 5 understanding wells). No radon-222 was detected above the proposed MCL-US upper threshold.

California↗

USGS2004

Occurrence and distribution of trace elements in snow, streams, and streambed sediments, Cape Krusenstern National Monument, Alaska, 2002-2003

Cape Krusenstern National Monument is located in Northwest Alaska. In 1985, an exchange of lands and interests in lands between the Northwest Alaska Native Association and the United States resulted in a 100-year transportation system easement for 19,747 acres in the monument. A road was then constructed along the easement from the Red Dog Mine, a large zinc concentrate producer and located northeast of the monument, through the monument to the coast and a port facility. Each year approximately 1.3 million tonnes of zinc and lead concentrate are transported from the Red Dog Mine via this access road. Concern about the possible deposition of cadmium, lead, zinc and other trace elements in the monument was the basis of a cooperative project with the National Park Service. Concentrations of dissolved cadmium, dissolved lead, and dissolved zinc from 28 snow samples from a 28 mile by 16 mile grid were below drinking water standards. In the particulate phase, approximately 25 percent of the samples analyzed for these trace elements were higher than the typical range found in Alaska soils. Boxplots of concentrations of these trace elements, both in the dissolved and particulate phase, indicate higher concentrations north of the access road, most likely due to the prevailing southeast wind. The waters of four streams sampled in Cape Krusenstern National Monument are classified as calcium bicarbonate. Trace-element concentrations from these streams were below drinking water standards. Median concentrations of 39 trace elements from streambed sediments collected from 29 sites are similar to the median concentrations of trace elements from the U.S. Geological Survey?s National Water-Quality Assessment database. Statistical differences were noted between trace-element concentrations of cadmium, lead, and zinc at sites along the access road and sites north and south of the access road; concentrations along the access road being higher than north or south of the road. When normalized to 1 percent organic carbon, the concentrations of these trace elements are not expected to be toxic to aquatic life when compared to criteria established by the Canadian government and other recent research.

Scientific Investigations Report↗

USGS1994

Assessment of concentrations of trace elements in ground water and soil at the Small-Arms Firing Range, Shaw Air Force Base, South Carolina

Ground-water samples were collected from four shallow water-table aquifer observation wells beneath the Small-Arms Firing Range study area at Shaw Air Force Base. Water-chemistry analyses indicated that total lead concentrations in shallow ground water beneath the study area do not exceed the U.S. Environmental Protection Agency maximum contaminant level established for lead in drinking water (0.05 milligrams per liter). All other trace element total concentrations in ground water beneath the study area were at or below the detection limit of the analytical methodology.

South Carolina↗

USGS2012

Origin and characteristics of discharge at San Marcos Springs based on hydrologic and geochemical data (2008-10), Bexar, Comal, and Hays Counties, Texas

The Edwards aquifer in south-central Texas is a productive and important water resource. Several large springs issuing from the aquifer are major discharge points, popular locations for recreational activities, and habitat for threatened and endangered species. Discharges from Comal and San Marcos Springs, the first and second largest spring complexes in Texas, are used as thresholds in groundwater management strategies for the Edwards aquifer. Comal Springs is generally understood to be supplied by predominantly regional groundwater flow paths; the hydrologic connection of San Marcos Springs with the regional flow system, however, is less understood. During November 2008–December 2010, a hydrologic and geochemical investigation of San Marcos Springs was conducted by the U.S. Geological Survey (USGS) in cooperation with the San Antonio Water System. The primary objective of this study was to define and characterize sources of discharge from San Marcos Springs. During this study, hydrologic conditions transitioned from exceptional drought (the dry period, November 1, 2008 to September 8, 2009) to wetter than normal (the wet period, September 9, 2009 to December 31, 2010), which provided the opportunity to investigate the hydrogeology of San Marcos Springs under a wide range of hydrologic conditions. Water samples were collected from streams, groundwater wells, and springs at and in the vicinity of San Marcos Springs, including periodic (routine) sampling (every 3–7 weeks) and sampling in response to storms. Samples were analyzed for major ions, trace elements, nutrients, and selected stable and radiogenic isotopes (deuterium, oxygen, carbon, strontium). Additionally, selected physicochemical properties were measured continuously at several sites, and hydrologic data were compiled from other USGS efforts (stream and spring discharge). Potential aquifer recharge was evaluated from local streams, and daily recharge or gain/loss estimates were computed for several local streams. Local rainfall and recharge events were compared with physicochemical properties and geochemical variability at San Marcos Springs, with little evidence for dilution by local recharge.

Texas↗

USGS2015

Groundwater quality data in 15 GAMA study units: results from the 2006–10 Initial sampling and the 2009–13 resampling of wells, California GAMA Priority Basin Project

The Priority Basin Project (PBP) of the Groundwater Ambient Monitoring and Assessment (GAMA) program was developed in response to the Groundwater Quality Monitoring Act of 2001 and is being conducted by the U.S. Geological Survey (USGS) in cooperation with the California State Water Resources Control Board (SWRCB). From May 2004 to March 2012, the GAMA-PBP collected samples from more than 2,300 wells in 35 study units across the State. Selected wells in each study unit were sampled again approximately 3 years after initial sampling as part of an assessment of temporal trends in water quality by the GAMA-PBP. This triennial (every 3 years) trend sampling of GAMA-PBP study units concluded in December 2013. Fifteen of the study units, initially sampled between January 2006 and June 2010 and sampled a second time between April 2009 and April 2013 to assess temporal trends, are the subject of this report. The initial sampling was designed to provide a spatially unbiased assessment of the quality of untreated groundwater used for public water supplies in the 15 study units. In these study units, 730 wells were selected by using a spatially distributed, randomized grid-based method to provide statistical representation of the areas assessed (grid wells, also called “status wells”). Approximately 3 years after the initial sampling, 93 of the previously sampled status wells (approximately 10 percent in each study unit) were randomly selected for trend sampling (“trend wells”). The 15 study units sampled for trends were distributed among 4 hydrogeologic provinces: Central Valley, Basin and Range, Desert, and Transverse and selected Peninsular Ranges. The total number of status wells sampled, along with those sampled again for trends, varied by study unit. In the Central Valley hydrogeologic province, the numbers of status wells and trend wells in each study unit were as follows: Kern County subbasin study unit—47 status wells, 5 trend wells Central Eastside San Joaquin Basin study unit—58 status wells, 6 trend wells Middle Sacramento Valley study unit—71 status wells, 8 trend wells Northern Sacramento Valley study unit—43 status wells, 4 trend wells Madera–Chowchilla study unit—30 status wells, 4 trend wells Western San Joaquin Valley study unit—39 status wells, 4 trend wells. The Basin and Range hydrogeologic province had only one study unit: Owens and Indian Wells Valleys study unit—53 status wells, 6 trend wells. In the Desert hydrogeologic province, the numbers of wells were as follows: Coachella Valley study unit—19 status wells 4 trend wells Colorado River study unit—20 status wells, 3 trend wells Antelope Valley study unit—56 status wells, 6 trend wells Mojave study unit—52 status wells, 7 trend wells Borrego Valley, Central Desert and Low-Use Basins of the Mojave and Sonoran Deserts study unit—49 status wells, 6 trend wells. In the Transverse and Selected Peninsular Ranges hydrogeologic province, the numbers of wells were as follows: Coastal Los Angeles Basin study unit—61 status wells, 8 trend wells Upper Santa Ana Watershed study unit—90 status wells, 16 trend wells Santa Clara River Valley study unit—42 status wells, 6 trend wells. The groundwater samples were analyzed for a number of synthetic organic constituents (volatile organic compounds, pesticides, and pesticide degradates), constituents of special interest (perchlorate, N -nitrosodimethylamine [NDMA], and 1,2,3-trichloropropane [1,2,3-TCP]), and naturally occurring inorganic constituents (nutrients, major and minor ions, and trace elements). Naturally occurring isotopes (tritium, carbon-14, and stable isotopes of hydrogen and oxygen in water) also were measured to help identify processes affecting groundwater quality and the sources and ages of the sampled groundwater. More than 200 constituents and water-quality indicators were investigated. Quality-control samples (blanks, replicates, or samples for matrix spikes) were collected at 34 percent of the trend wells, and the results for these samples were used to evaluate the quality of the data for the groundwater samples. On the basis of detections in laboratory and field blanks in samples from GAMA-PBP study units, including the study units presented here, some groundwater results were adjusted in this report. Differences between replicate samples were mostly within acceptable ranges, indicating acceptably low variability in analytical results. Median matrix-spike recoveries were within the acceptable range (70 to 130 percent) for 189 of the 224 compounds for which matrix spikes were analyzed (84 percent). This study did not attempt to evaluate the quality of water delivered to consumers. After withdrawal, groundwater used for drinking water typically is treated, disinfected, and blended with other waters to attain acceptable water quality. The benchmarks used in this report apply to treated water that is served to the consumer, not to untreated groundwater. To provide some context for the results, however, concentrations of constituents measured in these groundwater samples were compared with benchmarks established by the U.S. Environmental Protection Agency and California Department of Public Health. Comparisons between data collected for this study and benchmarks for drinking-water quality are for illustrative purposes only and are not indicative of compliance or non-compliance with those benchmarks. Most constituents that were detected in groundwater samples from the trend wells were found at concentrations less than drinking-water benchmarks. Two volatile organic compounds (VOCs)—tetrachloroethene and trichloroethene—were detected in samples from one or more wells at concentrations greater than their health-based benchmarks, and three VOCs—chloroform, tetrachloroethene, and trichloroethene—were detected in at least 10 percent of the trend-well samples from the initial sampling period and the later trend sampling period. No pesticides were detected at concentrations near or greater than their health-based benchmarks. Three pesticide constituents—atrazine, deethylatrazine, and simazine—were detected in more than 10 percent of the trend-well samples in both sampling periods. Perchlorate, a constituent of special interest, was detected at a concentration greater than its health-based benchmark in samples from one trend well in the initial sampling and trend sampling periods, and in an additional trend well sample only in the trend sampling period. Most detections of nutrients, major and minor ions, and trace elements in samples from trend wells were less than health-based benchmarks in both sampling periods. Exceptions included nitrate, fluoride, arsenic, boron, molybdenum, strontium, and uranium; these were all detected at concentrations greater than their health-based benchmarks in at least one well sample in both sampling periods. Lead and vanadium were detected above their health-based benchmarks in one sample each collected in the initial sampling period only. The isotopic ratios of oxygen and hydrogen in water and the activities of tritium and carbon-14 generally changed little between sampling periods.

California↗