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USGS2009

Quality of Water from Domestic Wells in Principal Aquifers of the United States, 1991-2004

As part of the National Water-Quality Assessment Program of the U.S. Geological Survey (USGS), water samples were collected during 1991-2004 from domestic wells (private wells used for household drinking water) for analysis of drinking-water contaminants, where contaminants are considered, as defined by the Safe Drinking Water Act, to be all substances in water. Physical properties and the concentrations of major ions, trace elements, nutrients, radon, and organic compounds (pesticides and volatile organic compounds) were measured in as many as 2,167 wells; fecal indicator bacteria and radionuclides also were measured in some wells. The wells were located within major hydrogeologic settings of 30 regionally extensive aquifers used for water supply in the United States. One sample was collected from each well prior to any in-home treatment. Concentrations were compared to water-quality benchmarks for human health, either U.S. Environmental Protection Agency (USEPA) Maximum Contaminant Levels (MCLs) for public water supplies or USGS Health-Based Screening Levels (HBSLs). No individual contaminant was present in concentrations greater than available health benchmarks in more than 8 percent of the sampled wells. Collectively, however, about 23 percent of wells had at least 1 contaminant present at concentrations greater than an MCL or HBSL, based on analysis of samples from 1,389 wells in which most contaminants were measured. Radon, nitrate, several trace elements, fluoride, gross alpha- and beta-particle radioactivity, and fecal indicator bacteria were found most frequently (in one or more percent of wells) at concentrations greater than benchmarks and, thus, are of potential concern for human health. Radon concentrations were greater than the lower of two proposed MCLs (300 picocuries per liter or pCi/L) in about 65 percent of the wells and greater than the higher proposed MCL (4,000 pCi/L) in about 4 percent of wells. Nitrate, arsenic, manganese, strontium, and gross alpha-particle radioactivity (uncorrected) each were present at levels greater than MCLs or HBSLs in samples from about 5 to 7 percent of the wells; boron, fluoride, uranium, and gross beta-particle radioactivity were present at levels greater than MCLs or HBSLs in about 1 to 2 percent of the wells. Total coliform and Escherichia coli bacteria were detected in about 34 and 8 percent, respectively, of sampled wells. Thus, with the exception of nitrate and fecal indicator bacteria, the contaminants that were present in the sampled wells most frequently at concentrations greater than human-health benchmarks were naturally occurring. Anthropogenic organic compounds were frequently detected at low concentrations, using typical analytical detection limits of 0.001 to 0.1 micrograms per liter, but were seldom present at concentrations greater than MCLs or HBSLs. The most frequently detected compounds included the pesticide atrazine, its degradate deethylatrazine, and the volatile organic compounds chloroform, methyl tert-butyl ether, perchloroethene, and dichlorofluoromethane. Only 7 of 168 organic compounds were present in samples at concentrations greater than MCLs or HBSLs, each in less than 1 percent of wells. These were diazinon, dibromochloroprane, dinoseb, dieldrin, ethylene dibromide, perchloroethene, and trichloroethene. Overall, concentrations of any organic compound greater than MCLs or HBSLs were present in 0.8 percent of wells, and concentrations of any organic compound greater than one-tenth of MCLs or HBSLs were present in about 3 percent of wells. Several other properties and contaminants were measured at values or concentrations outside of recommended ranges for drinking water for aesthetic quality (for example, taste or odor) or other non-health reasons. About 16 percent of the sampled wells had pH values less than (14.4 percent) or greater than (1.9 percent) the USEPA recommended range of 6.5 to 8.5. Total dissolved solids were greater than th

Scientific Investigations Report↗

USGS2008

Hydrochemical Regions of the Glacial Aquifer System, Northern United States, and Their Environmental and Water-Quality Characteristics

The glacial aquifer system in the United States is a large (953,000 square miles) regional aquifer system of heterogeneous composition. As described in this report, the glacial aquifer system includes all unconsolidated geologic material above bedrock that lies on or north of the line of maximum glacial advance within the United States. Examining ground-water quality on a regional scale indicates that variations in the concentrations of major and minor ions and some trace elements most likely are the result of natural variations in the geologic and physical environment. Study of the glacial aquifer system was designed around a regional framework based on the assumption that two primary characteristics of the aquifer system can affect water quality: intrinsic susceptibility (hydraulic properties) and vulnerability (geochemical properties). The hydrochemical regions described in this report were developed to identify and explain regional spatial variations in ground-water quality in the glacial aquifer system within the hypothetical framework context. Data analyzed for this study were collected from 1991 to 2003 at 1,716 wells open to the glacial aquifer system. Cluster analysis was used to group wells with similar ground-water concentrations of calcium, chloride, fluoride, magnesium, potassium, sodium, sulfate, and bicarbonate into five unique groups. Maximum Likelihood Classification was used to make the extrapolation from clustered groups of wells, defined by points, to areas of similar water quality (hydrochemical regions) defined in a geospatial model. Spatial data that represented average annual precipitation, average annual temperature, land use, land-surface slope, vertical soil permeability, average soil clay content, texture of surficial deposits, type of surficial deposit, and potential for ground-water recharge were used in the Maximum Likelihood Classification to classify the areas so the characteristics of the hydrochemical regions would resemble the characteristics of the clusters. The result of the Maximum Likelihood Classification is a map showing five hydrochemical regions of the glacial aquifer system. Statistical analysis of ion concentrations (calcium, chloride, fluoride, magnesium, sodium, potassium, sulfate, and bicarbonate) in samples collected from wells completed in the glacial aquifer system illustrates that variations in water quality can be explained, in part, by related environmental characteristics that control the movement of ground water through the aquifer system. A comparison of median concentrations of chemical constituents in ground water among the five hydrochemical regions indicates that ground water in the Midwestern Agricultural Region, the Urban-Influenced Region, and the Western Agriculture and Grassland Region has the highest concentrations of major and minor ions, whereas ground water in the Northern and Great Lakes Forested Region and the Mountain and Coastal Forested Region has the lowest concentrations of these ions. Median concentrations of barium, arsenic, lithium, boron, strontium, and nitrite plus nitrate as nitrogen also are significantly different among the hydrochemical regions.

Scientific Investigations Report↗

USGS2014

Water-quality trends for selected sampling sites in the upper Clark Fork Basin, Montana, water years 1996-2010

A large-scale trend analysis was done on specific conductance, selected trace elements (arsenic, cadmium, copper, iron, lead, manganese, and zinc), and suspended-sediment data for 22 sites in the upper Clark Fork Basin for water years 1996–2010. Trend analysis was conducted by using two parametric methods: a time-series model (TSM) and multiple linear regression on time, streamflow, and season (MLR). Trend results for 1996–2010 indicate moderate to large decreases in flow-adjusted concentrations (FACs) and loads of copper (and other metallic elements) and suspended sediment in Silver Bow Creek upstream from Warm Springs. Deposition of metallic elements and suspended sediment within Warm Springs Ponds substantially reduces the downstream transport of those constituents. However, mobilization of copper and suspended sediment from floodplain tailings and stream banks in the Clark Fork reach from Galen to Deer Lodge is a large source of metallic elements and suspended sediment, which also affects downstream transport of those constituents. Copper and suspended-sediment loads mobilized from within this reach accounted for about 40 and 20 percent, respectively, of the loads for Clark Fork at Turah Bridge (site 20); whereas, streamflow contributed from within this reach only accounted for about 8 percent of the streamflow at Turah Bridge. Minor changes in FACs and loads of copper and suspended sediment are indicated for this reach during 1996–2010. Clark Fork reaches downstream from Deer Lodge are relatively smaller sources of metallic elements than the reach from Galen to Deer Lodge. In general, small decreases in loads and FACs of copper and suspended sediment are indicated for Clark Fork sites downstream from Deer Lodge during 1996–2010. Thus, although large decreases in FACs and loads of copper and suspended sediment are indicated for Silver Bow Creek upstream from Warm Springs, those large decreases are not translated to the more downstream reaches largely because of temporal stationarity in constituent transport relations in the Clark Fork reach from Galen to Deer Lodge. Unlike metallic elements, arsenic (a metalloid element) in streams in the upper Clark Fork Basin typically is mostly in dissolved phase, has less variability in concentrations, and has weaker direct relations with suspended-sediment concentrations and streamflow. Arsenic trend results for 1996–2010 indicate generally moderate decreases in FACs and loads in Silver Bow Creek upstream from Opportunity. In general, small temporal changes in loads and FACs of arsenic are indicated for Silver Bow Creek and Clark Fork reaches downstream from Opportunity during 1996–2010. Contribution of arsenic (from Warm Springs Ponds, the Mill-Willow bypass, and groundwater sources) in the Silver Bow Creek reach from Opportunity to Warm Springs is a relatively large source of arsenic. Arsenic loads originating from within this reach accounted for about 11 percent of the load for Clark Fork at Turah Bridge; whereas, streamflow contributed from within this reach only accounted for about 2 percent of the streamflow at Turah Bridge.

Montana↗

USGS2006

Recent (2003-05) water quality of Barton Springs, Austin, Texas, with emphasis on factors affecting variability

From 2003 to 2005, the U.S. Geological Survey, in cooperation with the Texas Commission on Environmental Quality, collected and analyzed water samples from the four springs (orifices) of Barton Springs in Austin, Texas (Upper, Main, Eliza, and Old Mill Springs), with the objective of characterizing water quality. Barton Springs is the major discharge point for the Barton Springs segment of the Edwards aquifer. A three-pronged sampling approach was used: physicochemical properties (including specific conductance and turbidity) were measured continuously; samples were collected from the four springs routinely every 2 weeks (during August-September 2003) to 3 weeks (during June 2004-June 2005) and analyzed for some or all major ions, nutrients, trace elements, soluble pesticides, and volatile organic compounds; and samples were collected from the four springs at more closely spaced intervals during the 2 weeks following two storms and analyzed for the same suite of constituents. Following the two storms, samples also were collected from five of the six major streams that provide recharge to Barton Springs. Spring discharge during both sample collection periods was above average (60 cubic feet per second or greater). Barton Springs was found to be affected by persistent low concentrations of atrazine (an herbicide), chloroform (a drinking-water disinfection by-product), and tetrachloroethene (a solvent). Increased recharge from the major recharging streams resulted in increased calcium, sulfate, atrazine, simazine, and tetrachloroethene concentrations and decreased concentrations of most other major ions, nitrate, and chloroform at one or more of the springs. These changes in concentration demonstrate the influence of water quality in recharging streams on water quality at the springs even during non-stormflow conditions. The geochemical compositions of the four springs indicate that Upper Spring is more contaminated and is influenced by a contributing flow path that is separate from those leading to other springs under all but stormflow conditions. Main, Eliza, and Old Mill Springs share at least one common flow path that contributes contaminants to the three springs. Old Mill Spring, however, is less affected by anthropogenic contaminants than the other springs and receives a greater component of water from a flow path whose geochemistry is influenced by water from the saline zone of the aquifer. At Main Spring, atrazine, simazine, chloroform, and tetrachloroethene concentrations increased following storms, describing breakthrough curves that peaked 2 days following rainfall; at Upper Spring, atrazine and simazine concentrations described breakthrough curves that peaked 1 day following rainfall. At both Main and Upper Springs, additional anthropogenic compounds were detected following storms. The geochemical response of the springs to recharge indicates that much of the transport occurs through conduits. When there is no flow in the recharging streams, ground water advects from the aquifer matrix into the conduits and is transported to the springs. When there is flow in the streams, recharge through the streambeds directly enters the conduit system and is transported to the springs. Following storms, surface runoff recharges through both interstream recharge features and streambeds, delivering runoff-related contaminants to Barton Springs.

Scientific Investigations Report↗

USGS2002

Quality of shallow ground water in areas of recent residential and commercial development, Wichita, Kansas, 2000

Water samples from 30 randomly distributed monitoring wells in areas of recent residential and commercial development (1960–96), Wichita, Kansas, were collected in 2000 as part of the High Plains Regional Ground-Water Study conducted by the U.S. Geological Survey's National Water-Quality Assessment (NAWQA) Program. The samples were analyzed for about 170 water-quality constituents that included chlorofluorocarbons, physical properties, dissolved solids and major ions, nutrients and dissolved organic carbon, trace elements, pesticide compounds, and volatile organic compounds. The purpose of this report is to provide an assessment of water quality in recharge to shallow ground water underlying areas of recent residential and commercial development and to determine the relation of ground-water quality to overlying urban land use. Analyses of water from the 30 monitoring wells for chlorofluorocarbons were used to estimate apparent dates of recharge. Water from 18 wells with nondegraded and uncontaminated chlorofluorocarbon concentrations had calculated apparent recharge dates that ranged from 1979 to 1990 with an average date of 1986. Water from 14 monitoring wells (47 percent) exceeded the 500-milligrams-per-liter Secondary Maximum Contaminant Level established by the U.S. Environmental Protection Agency for dissolved solids in drinking water. The Secondary Maximum Contaminant Levels of 250 milligrams per liter for chloride and sulfate were exceeded in water from one well. The source of the largest concentrations of dissolved solids and associated ions, such as chloride and sulfate, in shallow ground water in the study area probably is highly mineralized water moving out of the Arkansas River into the adjacent, unconsolidated deposits and mixing with the dominant calcium bicarbonate water in the deposits. Concentrations of most nutrients in water from the sampled wells were small, with the exception of nitrate. Although water from the sampled wells did not have nitrate concentrations larger than the 10-milligram-per-liter Maximum Contaminant Level for drinking water, water from 50 percent of the sampled wells showed nitrate enrichment (concentrations greater than 2.0 milligrams per liter). Most trace elements in water from the sampled wells were detected only in small concentrations, and few exceeded respective water-quality standards. Twenty percent of iron concentrations, 40 percent of manganese concentrations, 3 percent of arsenic concentrations, and 13 percent of uranium concentrations exceeded respective Maximum Contaminant Levels or Secondary Maximum Contaminant Levels. A total of 47 pesticide compounds were analyzed in ground-water samples during this study. Water from 73 percent of the wells sampled had detectable concentrations of one or more of 8 of these 47 compounds. The herbicide atrazine or its degradation product deethylatrazine were detected most frequently (in water from 70 percent of the sampled wells). Metolachlor was detected in water from 10 percent of the wells, and simazine was detected in water from 30 percent of the wells sampled. Other pesticides detected included dieldrin, pendimethalin, prometon, and tebuthiuron (each in water from 3 percent of the wells). All concentrations of these compounds were less than established Maximum Contaminant Levels. A total of 85 volatile organic compounds (VOCs) were analyzed in ground-water samples during this study. Water from 43 percent of the wells had a detectable concentration of one or more VOCs. Chloroform was the most frequently detected VOC (23 percent of the wells sampled).Seven other VOCs were detected in water at frequencies of 13 percent or less in the wells sampled. Concentrations of VOCs were less than respective Maximum Contaminant Levels, except one sample with a concentration of 9.0 micrograms per liter for tetrachloroethylene (Maximum Contaminant Level of 5.0 micrograms per liter). An analysis of hydraulic gradient, flow velocity, and residence time of the ground water indicated potential recharge areas that ranged from 0.8 to 2.8 miles upgradient of monitoring-well locations. Nineteen (63 percent) of these potential recharge areas were in agricultural areas or areas in transition from agricultural to residential and (or) commercial land use at the time water sampled from the monitoring wells was recharged to the shallow ground water. The occurrence of atrazine or deethylatrazine in water from 70 percent of the monitoring wells may indicate a historical agricultural land-use relation. This agricultural relation also may affect concentrations of other water-quality constituents of possible agricultural origin such as nitrate, which generally were in excess of background concentrations in shallow ground water.

Kansas↗

USGS2003

Framework for a ground-water quality monitoring and assessment program for California

The State of California uses more ground water than any other State in the Nation. With a population of over 30 million people, an agricultural economy based on intensive irrigation, large urban industrial areas, and naturally elevated concentrations of some trace elements, there is a wide range of contaminant sources that have the potential to contaminate ground water and limit its beneficial uses. In response to the many-and different-potential sources of ground-water contamination, the State of California has evolved an extensive set of rules and programs to protect ground-water quality, and agencies to implement the rules and programs. These programs have in common a focus on compliance with regulations governing chemical use and (or) ground-water quality. Although appropriate for, and successful at, their specific missions, these programs do not at present provide a comprehensive view of ground-water quality in the State of California. In October 2001, The California Assembly passed a bill, AB 599, establishing the Ground-Water- Quality Monitoring Act of 2001.' The goal of AB 599 is to improve Statewide comprehensive ground-water monitoring and increase availability of information about ground-water quality to the public. AB 599 requires the State Water Resources Control Board (SWRCB), in collaboration with an interagency task force (ITF) and a public advisory committee (PAC), to develop a plan for a comprehensive ground-water monitoring program. AB 599 specifies that the comprehensive program should be capable of assessing each ground-water basin in the State through direct and other statistically reliable sampling approaches, and that the program should integrate existing monitoring programs and design new program elements, as necessary. AB 599 also stresses the importance of prioritizing ground-water basins that provide drinking water. The United States Geological Survey (USGS), in cooperation with the SWRCB, and in coordination with the ITF and PAC, has developed a framework for a comprehensive ground-water-quality monitoring and assessment program for California. The proposed framework relies extensively on previous work conducted by the USGS through its National Water-Quality Assessment (NAWQA) program. In particular, the NAWQA program defines three types of ground-water assessment: (1) status, the assessment of the current quality of the ground-water resource; (2) trends, the detection of changes in water quality, and (3) understanding, assessing the human and natural factors that affect ground-water quality. A Statewide, comprehensive ground-water quality-monitoring and assessment program is most efficiently accomplished by applying uniform and consistent study-design and data-collection protocols to the entire State. At the same time, a comprehensive program should be relevant at a variety of scales, and therefore needs to retain flexibility to address regional and local issues. Consequently, many of the program components include a predominant element that will be consistently applied in all basins, and a secondary element that may be applied in specific basins where local conditions warrant attention.

Water-Resources Investigations Report↗

USGS2012

Groundwater levels and water-quality observations pertaining to the Austin Group, Bexar County, Texas, 2009-11

The U.S. Geological Survey, in cooperation with the San Antonio Water System, examined groundwater-level altitudes (groundwater levels) and water-quality data pertaining to the Austin Group in Bexar County, Texas, during 2009–11. Hydrologic data collected included daily mean groundwater levels collected at seven sites in the study area. Water-quality samples were collected at six sites in the study area and analyzed for major ions, nutrients, trace elements, organic carbon, and stable isotopes. The resulting datasets were examined for similarities between sites as well as similarities to data from the Edwards aquifer in Bexar County, Tex. Similarities in the groundwater levels between sites completed in the Austin Group and site J (State well AY-68-37-203; hereafter referred to as the “Bexar County index well”) which is completed in the Edwards aquifer might be indicative of groundwater interactions between the two hydrologic units as a result of nearby faulting or conduit flow. The groundwater levels measured at the sites in the study area exhibited varying degrees of similarity to the Bexar County index well. Groundwater levels at site A (State well AY-68-36-136) exhibited similar patterns as those at the Bexar County index well, but the hydrographs of groundwater levels were different in shape and magnitude in response to precipitation and groundwater pumping, and at times slightly offset in time. The groundwater level patterns measured at sites C, D, and E (State wells AY-68-29-513, AY-68-29-514, and AY-68-29-512, respectively) were not similar to those measured at the Bexar County index well. Groundwater levels at site F (State well AY-68-29-819) exhibited general similarities as those observed at the Bexar County index well; however, there were several periods of notable groundwater-level drawdowns at site F that were not evident at the Bexar County index well. These drawdowns were likely because of pumping from the well at site F. The groundwater levels at sites H and I (State wells AY-68-37-205 and AY-68-29-932, respectively) exhibited similar patterns as those at the Bexar County index well (coefficient of determination [R 2 ] of 0.99 at both wells), indicating there might be some degree of hydrologic connectivity to the Edwards aquifer. In general, the water-quality data indicated that the samples were representative of a calcium carbonate dominated system. The major ion chemistry and relations between magnesium to calcium molar ratios and 87 Sr/ 86 Sr isotopic ratios of samples collected from sites H and I indicated that the groundwater from these sites was most geochemically similar to groundwater collected from site B (State well AY-68-36-134), which is representative of groundwater in the Edwards aquifer. Of the sites sampled in this study, there appears to be varying hydrologic connectivity between groundwater from wells completed in the Austin Group and the Edwards aquifer.

Texas↗

USGS2015

Characterization of hydrology and water quality of Piceance Creek in the Alkali Flat area, Rio Blanco County, Colorado, March 2012

Previous studies by the U.S. Geological Survey identified Alkali Flat as an area of groundwater upwelling, with increases in concentrations of total dissolved solids, and streamflow loss, but additional study was needed to better characterize these observations. The U.S. Geological Survey, in cooperation with the Bureau of Land Management, White River Field Office, conducted a study to characterize the hydrology and water quality of Piceance Creek in the Alkali Flat area of Rio Blanco County, Colorado. Water-quality samples were collected at five springs on March 27, 2012, to determine field properties, major ions, trace elements, and stable isotopes of water. Major-ion and trace-element chemistry indicated that the springs sampled as part of this study were likely recharged by the bedrock aquifer. Isotopic values for the springs plotted close to that of groundwater from the Parachute Creek Member of the Green River Formation, and the isotopic values from both of these sources are similar to the values for Grand Mesa snow. Based on fluoride, lithium, and strontium concentrations, one spring appeared to have different source water than the other four springs. The spring also had higher concentrations of calcium, magnesium, and sulfate relative to the other four springs. Trace-element and major-ion data indicate that this spring was sourced from the Uinta Formation. It was likely the other four springs were primarily sourced from the lower part of the Parachute Creek Member of the Green River Formation as indicated by low sulfate concentrations and high fluoride, lithium, and boron concentrations. Water-quality samples were collected at 16 surface-water-quality sites on March 14, 2012, to determine field properties, major ions, and trace elements. Sodium was the dominant cation and concentrations increased steadily from upstream to downstream along the study reach. Calcium, magnesium, and potassium concentrations remained relatively stable along the study reach. Strontium concentrations were relatively stable along the study reach, whereas boron and lithium concentrations increased appreciably at site PC22031 and remained elevated to the end of the study reach. Loading profiles were used to further refine areas of spring and groundwater input and streamflow gains and losses. Although there was a minor gain in streamflow from sites PC21543 to PC21816 (58 to 59 cubic feet per second (ft 3 /s) during March 2014), the observed increase in dissolved solids load indicated groundwater contribution to Piceance Creek between these two sites. From sites PC22737 to PC22980, dissolved solids load decreased, which was not observed in concentration profiles and indicated that streamflow loss occurred between these two sites. Barium, boron, lithium, and strontium loads showed similar patterns to that of the major ions along the study reach and indicated similar areas of groundwater gain and loss. Boron and lithium load were not observed to decrease in a similar pattern to that of barium and strontium load which would suggest the contribution to the stream from sources with similar chemistry to that of spring sites PCSP2 through PCSP5. Sodium, chloride, and bicarbonate loads increased and decreased along the study reach in a pattern similar to that of dissolved solids load. A chemical mass balance was used to estimate the amount of groundwater and (or) spring water that contributed to the observed changes in water quality along Piceance Creek. This analysis indicated only 5 percent spring water would need to reach Piceance Creek to result in the observed changes in water quality. Instantaneous streamflow was measured from sites PC20133 to PC23721 during field reconnaissance (February 2012) and during synoptic sampling (March 2012). During both February and March, the study reach from sites PC20133 to PC23721 was a losing reach with net losses that ranged from 0.5 ft 3 /s (February) to 3 ft 3 /s (March). Observed changes in streamflow along the study reach helped to depict interactions between groundwater and surface water in the Alkali Flat area. Water-quality samples were collected at five surface-water sites in December 2010 that were sampled as part of a previous USGS study in 2000. Water-quality data collected during December 2010 showed no appreciable difference from water-quality data collected during December 2000 at the five sites.

Colorado↗

USGS2007

Hydrogeology of the Coconino Plateau and adjacent areas, Coconino and Yavapai Counties, Arizona

Two large, regional ground-water flow systems occur in the Coconino Plateau and adjacent areas: the C aquifer and the Redwall-Muav aquifer. The C aquifer occurs mainly in the eastern and southern parts of the 10,300-square-mile Coconino Plateau study area, and the Redwall-Muav aquifer underlies the entire study area. The C aquifer is a water-table aquifer for most of its occurrence with depths to water that range from a few hundred feet to more than 1,500 feet. In the western part of the Coconino Plateau study area, the C aquifer is dry except for small localized perched water-bearing zones decoupled from the C aquifer to the east. The Redwall-Muav aquifer underlies the C aquifer and ranges from at least 3,000 feet below land surface in the western part of the Coconino Plateau study area to more than 3,200 feet below land surface in the eastern part of the study area. The Redwall-Muav aquifer is a confined aquifer for most of its occurrence with hydraulic heads of several hundred to more than 500 feet above the top of the aquifer in the western part of the study area and more than 2,000 feet above the top of the aquifer in the eastern part of the study area near Flagstaff. In the eastern and northeast parts of the area, the C aquifer and the Redwall-Muav aquifer are in partial hydraulic connection through faults and other fractures. The water discharging from the two aquifers on the Coconino Plateau study area is generally of good quality for most intended uses. Water from sites in the lower Little Colorado River Canyon had high concentrations of most trace elements relative to other springs, rivers, and streams in the study area. Concentrations of barium, arsenic, uranium, and lead, and gross alpha radioactivity were greater than U.S. Environmental Protection Agency Maximum Contaminant Levels for drinking water at some sites. Ground water discharging to most springs, streams, and wells on the Coconino Plateau and in adjacent areas is a calcium magnesium bicarbonate type and has low concentrations of the major dissolved constituents. Ground water discharging from the Redwall-Muav aquifer to springs in the lower Little Colorado River Canyon is a mixture of water from the C aquifer and the Redwall-Muav aquifer and is a sodium chloride type with high concentrations of most major dissolved constituents. Concentrations of sulfate and chloride in ground water discharging from the Redwall-Muav aquifer at springs near the south rim of Grand Canyon increase toward the west. Water samples from the Verde River above Mormon Pocket had higher concentrations of most dissolved constituents than samples from springs that discharge from the Redwall-Muav aquifer at Mormon Pocket and in Sycamore Canyon. Water-chemistry data from C aquifer wells and springs in the Flagstaff area indicate that ground-water ages in the aquifer range from 7,000 years to modern and that samples were a mix of younger and older waters. Ground-water ages for the Redwall-Muav aquifer are estimated to range from 22,600 to 7,500 years, and low tritium values indicate that this water is older than water discharging from the C aquifer. Tritium and carbon-14 results indicate that ground water discharging at most springs and streams is a mixture of young and old ground waters, likely resulting from multiple flow paths and multiple recharge areas. Ground-water withdrawals in the study area increased from about 4,000 acre-feet per year prior to 1975, to about 20,000 acre-feet per year in 2003. About two-thirds of the water withdrawn is from the C aquifer and about one-third is from the Redwall-Muav aquifer. In the study area, most development of the C aquifer has occurred near Flagstaff. Development of the Redwall-Muav aquifer is more extensive in Verde Valley where water-bearing zones of the aquifer are closer to land surface. In recent years, however, development of the Redwall-Muav aquifer in the study area has increased in response to population growth and the atten

Scientific Investigations Report↗

USGS2004

Quality of water from shallow wells in the rice-growing area in southwestern Louisiana, 1999 through 2001

In 1999-2001, the U.S. Geological Survey installed and sampled 27 shallow wells in the rice-growing area in southwestern Louisiana as part of the Acadian-Pontchartrain Study Unit of the National Water-Quality Assessment Program. The purpose of this report is to describe the waulity of water from shallow wells in the rice-growing area and to relate that water quality to natural and anthropogenic activities, particularly rice agriculture. Ground-water samples were analyzed for general ground-water properties and about 150 water-quality constituents, including major inorganic ions, trace elements, nutrients, dissolved organic carbon (DOC), pesticides, radon, chloroflourocarbons, and selected stable isotopes. Dissolved solids concentrations for 17 wells exceeded the U.S. Environmental Protection Agency secondary minimum containment level of 500 milligrams per liter (mg/L) for drinking water. Concentrations for major pesticides generally were less than the maximum contaminant levels for drinking water. Two major inorganic ions, sulfate and chloride, and two trace elements, iron and manganese, had concentrations that were greater than the secondary maximum containment levels. Three nutrient concentrations were greater than 2 mg/L, a level that might indicate contamination from human activities, and one nutrient concentration (that for nitrite plus nitrite as nitrogen) was greater than the maximum contaminant level of 10 mg/L for drinking water. The median concentration for DOC was 0.5 mg/L, indicating naturally-occurring DOC conditions in the study area. Thirteen pesticides and 7 pesticide degradation products were detected in 14 of the 27 wells sampled. Bentazon, 2, 4-D, and molinate (three rice herbicides) were detected in water from four, one, and one wells, respectively, and malathion (a rice insecticide) was deteced in water fromone well. Low-level concentrations and few detections of nutrients and pesticides indicated that ground-water quality was affected slightly by anthropogenic activities. Quality-control samples, including field blanks, replicates, and spikes, indicated no bias in ground-water data from collection on analysis. Radon concentrations for 22 of the 24 wells sampled wer at or greater than the U.S. Environmental Protection Agency proposed maximum contaminant level of 300 picocuries per liter. Chlorofluorocarbon concentrations in selected wells indicated the apparent ages of the ground water varied with depth water level and ranged from about 17 to 49 years. The stable isotopes of hydrogen and oxygen in water molecules indicated the origin of ground water in the study area was rainwater that originated near the study area and that few geochemical or physical processes influenced the stable isotopic composition of the shallow ground water. The Spearman rank correlation was used to detemrine whther significant correlations existed between physical properties, selected chemical constituents, the number of pesticides detected, and the apparent age of water. The depth to ground water was positively correlated to the well depth and inversely correlated to dissolved solids and other constituents, such as radon, indicating the ground water was under unconfined or semiconfined conditions and more dilute with increasing depth. As the depth to ground water increased, the concentrations of dissolved solids and other constituents decreased, possibly because the deeper sands had a greater transmittal of ground water, which, over time, would flush out, or dilute, the concentrations of dissolved solids in the natural sediments. The apparent age of water was correlated inversely with nitrite plus nitrite concentration, indicating that as apparent age increased, the nitrite plus nitrite concentration decreased. No significant correlations existed between the number of pesticides detected and any of the physical or chemica

Water-Resources Investigations Report↗

USGS1990

Water quality of alluvial aquifers, Carroll and Guthrie counties, Iowa, with emphasis on the occurrence of nitrate and pesticides, 1986-87

Samples collected from wells in Carroll and Guthrie Counties, Iowa, were analyzed to describe the chemical quality of the ground water in shallow aquifers. The study began in June 1986 with the selection of 20 shallow wells in Carroll County and 22 shallow wells in Guthrie County. These wells were sampled in the summer and fall of 1986 and 1987. Samples from the wells were analyzed for major ions, nutrients, trace elements, radiochemicals, nitrate, and pesticides. Median and mean nitrate concentrations were 95 and 11 milligrams per liter. About 60 percent of the samples had nitrate concentrations greater than 5.0 milligrams per liter. Detectable concentrations of a least one pesticide were in 27 percent of the samples. Atrazine, the most prevalent pesticide, was detected in 25 percent of the samples; alachlor was detected in 6 percent; and cyanazine was detected in 5 percent. Dicamba, metolachlor, trifluralin, and2,4-D were detected in 2 percent or less of the samples. In the summer and fall 1986,43 and 45 percent of the water samples had nitrate concentrations larger than 10 milligrams per liter, the maximum contaminant level for public drinking water specified by the State of Iowa; in the summer and fall 1987,41 and 55 percent of the samples had nitrate concentrations larger than the maximum contaminant level. In the summer and fall 1986,23 and 18 percent of the samples contained detectable concentrations of at least one pesticide; in the summer and fall 1987,21 and 47 percent of the samples contained detectable concentrations of at least one pesticide. Detection frequencies ofatrazine, alachlor, and cyanazine increased for samples collected in October 1987. Pesticides were more frequently detected along Brushy Creek, and the East Nishnabotna, Middle, North Raccoon, and South Raccoon Rivers. However, pesticides also were detected along the Middle Raccoon and West Nishnabotna Rivers. Detection frequencies were greatest (50 percent) for the East Nishnabotna River and Middle River alluvial settings. Increased nitrate concentrations generally were observed in the shallower wells and were larger than those previously reported for shallow municipal wells. Pesticide detection relative to well depth was inconsistent with the trend observed for nitrate. Pesticide detection frequencies were greater for wells that were 40 to 80 feet deep (about 40 percent) than for wells less that 40 feet deep (about 20 percent). Of the water samples with nitrate concentrations greater than or equal to 5.0 milligrams per liter, 33 percent had detectable pesticide concentrations. Conversely, for those samples with detectable pesticide concentrations, 76 percent had nitrate concentrations larger than or equal to 5.0 milligrams per liter and 67 percent were larger than or equal to 10 milligrams per liter. The median concentration of nitrate for samples containing at least one detectable pesticide was 15 milligrams per liter and was greater than the overall median nitrate concentration of 95 milligrams per liter. The median for samples that did not contain a detectable pesticide was 73 milligrams per liter.

Iowa↗

USGS2007

Influence of Locally Derived Recharge on the Water Quality and Temperature of Springs in Hot Springs National Park, Arkansas

The hot springs of Hot Springs National Park consist of a mixture of water from two recharge components: a primary hot-water component and a secondary cold-water component. Widespread distribution of fractures enables mixing of the hot- and cold-water components of flow near the discharge area for the springs. Urbanization in the area near the hot springs of Hot Springs National Park has increased the potential for degradation of the quality of surface-water runoff and locally derived ground-water recharge to the hot springs. Previous studies by the U.S. Geological Survey have indicated that water from some cold-water springs and wells in the vicinity of Hot Springs, Arkansas, showed evidence of contamination and that water from locally derived cold-water recharge might contribute 25 percent of the total flow to the hot springs after storms. Water samples were collected during base-flow conditions at nine hot springs and two cold-water springs in September 2000. Nine hot springs and one cold-water spring were resampled in October 2001 after a storm that resulted in a measurable decrease in water temperature in selected hot springs. Water samples were analyzed for a variety of dissolved chemical constituents (nutrients, major ions, trace elements, pesticides, semivolatile compounds, isotopes, and radiochemicals), physical properties, field measurements, and bacteria. Comparison of analyses of samples collected during base-flow conditions from the springs in 2000 and during a storm event in 2001 with the results from earlier studies dating back to the late 1800's indicates that little change in major, minor, and trace constituent chemistry has occurred and that the water continues to be of excellent quality. Water-quality data show distinguishable differences in water chemistry of the springs during base-flow and stormflow conditions, indicating changing input of cold-water recharge relative to hot-water recharge. Silica, total dissolved solids, strontium, barium, and sulfate show statistically significant differences between the median values of base-flow and stormflow samples. While variations in these constituents do not degrade water quality, the differences do provide evidence of variability in the factors controlling water quality of the hot springs and show that water quality is influenced by the locally derived, cold-water component of flow to the springs. Water temperature was measured continuously (3-minute intervals) between August 2000 and October 2002 at four hot springs. Continuous water-temperature data at the springs provide no indication of persistent long-term change in water temperature through time. Short time-scale water-temperature decreases occur in response to mixing of hot-springs water with locally derived recharge after storm events; the magnitude of these decreases varied inversely with the amount of rainfall. Maximum decreases in water temperature for specific storms had a non-linear relation with the amount of precipitation measured for the events. Response time for water temperature to begin decreasing from baseline temperature as a result of storm recharge was highly variable. Some springs began decreasing from baseline temperature as quickly as 1 hour after the beginning of a storm; one spring had an 8-hour minimum response time to show a storm-related temperature decrease. Water-quality, water-temperature, isotopic, and radiochemical data provide multiple lines of evidence supporting the importance of the contribution of cold-water recharge to hot springs. All the springs sampled indicated some measure of influence from local recharge. Binary mixing models using silica and total dissolved solids indicate that cold-water recharge from stormflow contributes an estimated 10 to 31 percent of the flow of hot springs. Models using water temperature indicate that cold-water recharge from stormflow contributes an estimated 1 to 35 percent of the flow of the various hot springs. Alth

Scientific Investigations Report↗

USGS2015

Occurrence and transport of selected constituents in streams near the Stibnite mining area, Central Idaho, 2012–14

Mining of stibnite (antimony sulfide), tungsten, gold, silver, and mercury near the town of Stibnite in central Idaho has left a legacy of trace element contamination in local streams. Water-quality and streamflow monitoring data from a network of five streamflow-gaging stations were used to estimate trace-element and suspended-sediment loads and flow-weighted concentrations in the Stibnite mining area between 2012 and 2014. Measured concentrations of arsenic exceeded human health-based water-quality criteria at each streamflow-gaging station, except for Meadow Creek (site 2), which was selected to represent background conditions in the study area. Measured concentrations of antimony exceeded human health-based water-quality criteria at sites 3, 4, and 5. Regression models developed using the U.S. Geological Survey LOAD ESTimation (LOADEST) program showed that concentrated sources of arsenic and antimony are present in specific reaches along Meadow Creek and the East Fork of South Fork of the Salmon River (EFSFSR) between the EFSFSR at Stibnite (site 3) and the EFSFSR above Sugar Creek (site 4). Eighty percent of the arsenic and antimony loads were attributable to discrete reaches that accounted for 25 percent of the total streamflow in the study area. Streamflow was negatively correlated with arsenic and antimony concentrations, indicating groundwater sources. Continuously monitored specific conductance, alone or combined with continuously computed streamflow, was more significant than streamflow alone as a surrogate measure of dissolved arsenic and antimony concentrations. Surrogate regression models (with coefficients of determination ranging from 0.96 to 0.65) can be used to estimate arsenic and antimony concentrations in real time at all five streamflow-gaging stations. LOADEST model simulation results indicated hysteresis in transport of suspended sediment and sediment-associated constituents. Predictor variables that account for streamflow variability reduced model bias and root mean square error when included in regression models used to estimate concentrations and loads of suspended sediment, total aluminum, total lead, and total mercury. Ninety-eight percent of the estimated total mercury load transported downstream of the study area is attributable to Sugar Creek. A maximum concentration of 26 micrograms per liter was measured in Sugar Creek during May 2013 when snowmelt runoff occurred during a single peak in the hydrograph. Monitoring and modeling results indicate sediment and sediment-associated constituent concentrations and loads increase along Meadow Creek, likely because of the inflow of the East Fork of Meadow Creek, and decrease between sites 3 and 4 because the Glory Hole is trapping sediments. Sugar Creek (site 5) accounted for most of the sediment and sediment-associated constituent loading leaving the study area because loads from the East Fork of Meadow Creek remained trapped in the Glory Hole. Additionally, total mercury was detected at all five streamflow-gaging stations, and sampled mercury concentrations exceeded Idaho ambient water-quality criteria at all five streamflow-gaging stations.

Idaho↗

USGS2017

Water quality, sources of nitrate, and chemical loadings in the Geronimo Creek and Plum Creek watersheds, south-central Texas, April 2015–March 2016

Located in south-central Texas, the Geronimo Creek and Plum Creek watersheds have long been characterized by elevated nitrate concentrations. From April 2015 through March 2016, an assessment was done by the U.S. Geological Survey, in cooperation with the Guadalupe-Blanco River Authority and the Texas State Soil and Water Conservation Board, to characterize nitrate concentrations and to document possible sources of elevated nitrate in these two watersheds. Water-quality samples were collected from stream, spring, and groundwater sites distributed across the two watersheds, along with precipitation samples and wastewater treatment plant (WWTP) effluent samples from the Plum Creek watershed, to characterize endmember concentrations and isotopic compositions from April 2015 through March 2016. Stream, spring, and groundwater samples from both watersheds were collected during four synoptic sampling events to characterize spatial and temporal variations in water quality and chemical loadings. Water-quality and -quantity data from the WWTPs and stream discharge data also were considered. Samples were analyzed for major ions, selected trace elements, nutrients, and stable isotopes of water and nitrate. The dominant land use in both watersheds is agriculture (cultivated crops, rangeland, and grassland and pasture). The upper part of the Plum Creek watershed is more highly urbanized and has five major WWTPs; numerous smaller permitted wastewater outfalls are concentrated in the upper and central parts of the Plum Creek watershed. The Geronimo Creek watershed, in contrast, has no WWTPs upstream from or near the sampling sites. Results indicate that water quality in the Geronimo Creek watershed, which was evaluated only during base-flow conditions, is dominated by groundwater, which discharges to the stream by numerous springs at various locations. Nitrate isotope values for most Geronimo Creek samples were similar, which indicates that they likely have a common source (or sources) of nitrate. Nitrate sources in the Geronimo Creek watershed include a predominance of nitrate from fertilizer applications, as well as a contribution from septic systems. Additional nitrate loading from these sources is ongoing. Chemical loadings of dissolved solids, chloride, and sulfate varied little among sampling events and were low at most sites because of low streamflow. In contrast to the Geronimo Creek watershed, nitrate sources in the Plum Creek watershed are dominated by effluent discharge from the major WWTPs in the upper and central parts of the watershed. Results indicate that discharge from these WWTPs accounts for the majority of base flow in the watershed. Nitrate concentrations in Plum Creek were dependent on flow conditions, with the highest concentrations measured at lower flows, when flow is dominated by WWTP effluent discharge. In addition to WWTP effluent discharge, the Plum Creek watershed, similar to the Geronimo Creek watershed, also is affected by historical and current loading of nitrate from fertilizer applications and from septic systems in the watershed. Chemical loadings of dissolved solids, chloride, sulfate, and nitrate in Plum Creek at lower flow conditions are highest at the upstream sites and decrease downstream as distance from the WWTPs increases, which is consistent with WWTP effluent as an important control on water quality. Under higher flow conditions, however, nitrate loads to Plum Creek increased by about a factor of three. These higher nitrate loads cannot be accounted for by WWTP effluent discharge from the five major WWTPs in the watershed. This additional loading indicates that nitrate is exported from the northeastern part of the watershed. In the lower part of the Plum Creek watershed, higher concentrations of dissolved solids, chloride, and sulfate occur, which might be affected by produced water associated with oil and gas exploration, or mixing with saline groundwater.

Texas↗

USGS2002

Statistical analysis of stream water-quality data and sampling network design near Oklahoma City, central Oklahoma, 1977-1999

Water-quality data collected from 1993-99 at five sites on Bluff, Deer, and Chisholm Creeks and from 1988-99 at five sites in the North Canadian River indicated that there were significant differences in constituent values among sites for water properties, major ions, trace elements, nutrients, turbidity, pesticides, and bacteria. Concentrations of dissolved solids and sulfate generally decreased as streams flowed through the Oklahoma City urban area. Concentrations of organic carbon, nitrogen and phosphorus compounds, lindane, and 2,4-D, and frequencies of detection of pesticides increased in the North Canadian River as it flowed through the urban area. Volatile organic compounds were not detected in samples collected quarterly from 1988-90 at sites on the North Canadian River. Concentrations of some compounds, including dissolved oxygen, sulfate, chloride, ammonia, manganese, diazinon, dieldrin, and fecal coliform bacteria periodically exceeded Federal or state water-quality standards at some sites. Regression analyses were used to identify trends in constituent concentrations related to streamflow, season, and time. Trends for some constituents were indicated at all sites, but most trends were sitespecific. Seasonal trends were evident for several constituents: suspended solids, organic nitrogen, and biochemical oxygen demand were greatest during summer. Dissolved oxygen, ammonia, and nitrite plus nitrate-nitrogen were greatest during winter. Concentrations of dissolved oxygen, fluoride, sulfate, total suspended solids, iron, and manganese generally increased with time. Concentrations of chloride, nitrite plus nitrate-nitrogen, dissolved phosphorus, dissolved orthophosphate, biochemical oxygen demand, dieldrin, and lindane decreased with time. There was relatively little change in land use from the late 1970s to the mid-1990s due to relatively modest rates of population growth in the study area during that period. Most changes in water quality in these streams and rivers may be due to changes in chemical use and wastewater treatment practices. The sampling network was evaluated with respect to areal coverage, sampling frequency, and analytical schedules. Areal coverage could be expanded to include one additional watershed that is not part of the current network. A new sampling site on the North Canadian River might be useful because of expanding urbanization west of the city, but sampling at some other sites could be discontinued or reduced based on comparisons of data between the sites. Additional real-time or periodic monitoring for dissolved oxygen may be useful to prevent anoxic conditions in pools behind new low-water dams. The sampling schedules, both monthly and quarterly, are adequate to evaluate trends, but additional sampling during flow extremes may be needed to quantify loads and evaluate water-quality during flow extremes. Emerging water-quality issues may require sampling for volatile organic compounds, sulfide, total phosphorus, chlorophyll- a , Esherichia coli , and enterococci, as well as use of more sensitive laboratory analytical methods for determination of cadmium, mercury, lead, and silver.

Oklahoma↗

USGS2005

Water-Quality Assessment of the Yellowstone River Basin, Montana and Wyoming-Water Quality of Fixed Sites, 1999-2001

The National Water-Quality Assessment Program of the U.S. Geological Survey initiated an assessment in 1997 of the quality of water resources in the Yellowstone River Basin. Water-quality samples regularly were collected during 1999-2001 at 10 fixed sites on streams representing the major environmental settings of the basin. Integrator sites, which are heterogeneous in land use and geology, were established on the mainstem of the Yellowstone River (4 sites) and on three major tributaries?Clarks Fork Yellowstone River (1 site), the Bighorn River (1 site), and the Powder River (1 site). Indicator sites, which are more homogeneous in land use and geology than the integrator sites, were located on minor tributaries with important environmental settings?Soda Butte Creek in a mineral resource area (1 site), the Tongue River in a forested area (1 site), and the Little Powder River in a rangeland area (1 site). Water-quality sampling frequency generally was at least monthly and included field measurements and laboratory analyses of fecal-indicator bacteria, major ions, dissolved solids, nutrients, trace elements, pesticides, and suspended sediment. Median concentrations of fecal coliform and Escherichia coli were largest for basins that were predominantly rangeland and smallest for basins that were predominantly forested. Concentrations of fecal coliform and Escherichia coli significantly varied by season (p-value <0.001); the smallest median concentrations were during January?March and the largest median concentrations were during April?June. Fecal-coliform concentrations exceeded the U.S. Environmental Protection Agency recommended limit for a single sample of 400 colonies per 100 milliliters in 2.6 percent of all samples. Escherichia coli concentrations exceeded the U.S. Environmental Protection Agency recommended limit for a single sample of 298 colonies per 100 milliliters for moderate use, full-body contact recreation in 7.6 percent of all samples. Variations in water type in the basin are reflective of the diverse geologic terrain in the Yellowstone River Basin. The water type of Soda Butte Creek and the Tongue River was calcium bicarbonate. These two sites are in forested and mountainous areas where igneous rocks and Paleozoic-era and Mesozoic-era sedimentary rocks are the dominant geologic groups. The water type of the Little Powder River was sodium sulfate. The Little Powder River originates in the plains, and geology of the basin is nearly homogenous with Tertiary-period sedimentary rocks. Water type of the Yellowstone River changed from a mixed-cation bicarbonate type upstream to a mixed-cation sulfate type downstream. Dissolved-solids concentrations ranged from fairly dilute in Soda Butte Creek, which had a median concentration of 118 milligrams per liter, to concentrated in the Little Powder River, which had a median concentration of 2,840 milligrams per liter. Nutrient concentrations generally were small and reflect the relatively undeveloped conditions in the basin; however, some correlations were made with anthropogenic factors. Median dissolved-nitrate concentrations in all samples from the fixed sites ranged from 0.04 milligram per liter to 0.54 milligram per liter. Flow-weighted mean dissolved-nitrate concentrations were positively correlated with increasing agricultural land use and rangeland on alluvial deposits upstream from the sites and negatively correlated with increasing forested land. Ammonia concentrations generally were largest in samples collected from the Yellowstone River at Corwin Springs, Montana, which is downstream from Yellowstone National Park and receives discharge from geothermal waters that are high in ammonia. Median total-phosphorus concentrations ranged from 0.007 to 0.18 milligram per liter. Median total-phosphorus concentrations exceeded the U.S. Environmental Protection Agency's recommended goal of 0.10 milligram per liter for preventing nuisance plant growth for samples collec

Scientific Investigations Report↗

USGS2009

Quality of Shallow Groundwater and Drinking Water in the Mississippi Embayment-Texas Coastal Uplands Aquifer System and the Mississippi River Valley Alluvial Aquifer, South-Central United States, 1994-2004

The Mississippi embayment-Texas coastal uplands aquifer system is an important source of drinking water, providing about 724 million gallons per day to about 8.9 million people in Texas, Louisiana, Mississippi, Arkansas, Missouri, Tennessee, Kentucky, Illinois, and Alabama. The Mississippi River Valley alluvial aquifer ranks third in the Nation for total withdrawals of which more than 98 percent is used for irrigation. From 1994 through 2004, water-quality samples were collected from 169 domestic, monitoring, irrigation, and public-supply wells in the Mississippi embayment-Texas coastal uplands aquifer system and the Mississippi River Valley alluvial aquifer in various land-use settings and of varying well capacities as part of the U.S. Geological Survey's National Water-Quality Assessment Program. Groundwater samples were analyzed for physical properties and about 200 water-quality constituents, including total dissolved solids, major inorganic ions, trace elements, radon, nutrients, dissolved organic carbon, pesticides, pesticide degradates, and volatile organic compounds. The occurrence of nutrients and pesticides differed among four groups of the 114 shallow wells (less than or equal to 200 feet deep) in the study area. Tritium concentrations in samples from the Holocene alluvium, Pleistocene valley trains, and shallow Tertiary wells indicated a smaller component of recent groundwater than samples from the Pleistocene terrace deposits. Although the amount of agricultural land overlying the Mississippi River Valley alluvial aquifer was considerably greater than areas overlying parts of the shallow Tertiary and Pleistocene terrace deposits wells, nitrate was rarely detected and the number of pesticides detected was lower than other shallow wells. Nearly all samples from the Holocene alluvium and Pleistocene valley trains were anoxic, and the reducing conditions in these aquifers likely result in denitrification of nitrate. In contrast, most samples from the Pleistocene terrace deposits in Memphis, Tennessee, were oxic, and the maximum nitrate concentration measured was 6.2 milligrams per liter. Additionally, soils overlying the Holocene alluvium and Pleistocene valley trains, generally in areas near the wells, had lower infiltration rates and higher percentages of clay than soils overlying the shallow Tertiary and Pleistocene terrace deposits wells. Differences in these soil properties were associated with differences in the occurrence of pesticides. Pesticides were most commonly detected in samples from wells in the Pleistocene terrace deposits, which generally had the highest infiltration rates and lowest clay content. Median dissolved phosphorus concentrations were 0.07, 0.11, and 0.65 milligram per liter in samples from the shallow Tertiary, Pleistocene valley trains, and Holocene alluvium, respectively. The widespread occurrence of dissolved phosphorus at concentrations greater than 0.02 milligram per liter suggests either a natural source in the soils or aquifer sediments, or nonpoint sources such as fertilizer and animal waste or a combination of natural and human sources. Although phosphorus concentrations in samples from the Holocene alluvium were weakly correlated to concentrations of several inorganic constituents, elevated concentrations of phosphorus could not be attributed to a specific source. Phosphorus concentrations generally were highest where samples indicated anoxic and reducing conditions in the aquifers. Elevated dissolved phosphorus concentrations in base-flow samples from two streams in the study area suggest that transport of phosphorus with groundwater is a potential source contributing to high yields of phosphorus in the lower Mississippi River basin. Water from 55 deep wells (greater than 200 feet deep) completed in regional aquifers of Tertiary age represent a sample of the principal aquifers used for drinking-water supply in the study area. The wells were screened in both confined and

Scientific Investigations Report↗

USGS2008

Geochemical trends and natural attenuation of RDX, nitrate, and perchlorate in the hazardous test area Fractured-Granite aquifer, White Sands Missile Range, New Mexico, 1996-2006

A fractured-granite aquifer at White Sands Missile Range is contaminated with the explosive compound RDX, nitrate, and perchlorate (oxidizer associated with rocket propellant) from the previous use of the Open Burn/Open Detonation site at the Hazardous Test Area. RDX, nitrate, and perchlorate ground-water concentrations were analyzed to examine source characteristics, spatial and temporal variability, and the influence of the natural attenuation processes of dilution and degradation in the Hazardous Test Area fractured-granite aquifer. Two transects of ground-water wells from the existing monitoring-site network - one perpendicular to ground-water flow (transect A-A') and another parallel to ground-water flow (transect B-B') - were selected to examine source characteristics and the spatial and temporal variability of the contaminant concentrations. Ground-water samples collected in 2005 from a larger sampling of monitoring sites than the two transects were analyzed for various tracers including major ions, trace elements, RDX degradates, dissolved gases, water isotopes, nitrate isotopes, and sulfate isotopes to examine the natural attenuation processes of dilution and degradation. Recharge entrains contaminants at the site and transports them downgradient towards the Tularosa Basin floor through a poorly connected fracture system(s). From 1996 to 2006, RDX, nitrate, and perchlorate concentrations in ground water downgradient from the Open Burn/Open Detonation site have been relatively stable. RDX, nitrate, and perchlorate in ground water from wells near the site indicate dispersed contaminant sources in and near the Open Burn/Open Detonation pits. The sources of RDX and nitrate in the pit area have shifted with time, and the shift correlates with the regrading of the south and east berms of each pit in 2002 and 2003 following closure of the site. The largest RDX concentrations were in ground water about 0.1 mile downgradient from the pits, the largest perchlorate concentrations were in ground water about 0.15 mile downgradient from the pits, and the largest nitrate concentrations were in ground water about 0.25 mile down-gradient from the pits. Strong and moderate correlation of water level and the contaminant concentrations near the source areas and low correlation outside and downgradient from the source areas indicates a diminishing of the water level/contaminant relation with downgradient flow. Ground water was not progressively older at all locations downgradient from the Open Burn/Open Detonation site indicating multiple recharge areas. Major ion and strontium concentrations and d2H and d18O values identified similar sources of recharge waters comprising the aquifer except along the basin periphery where recharge water may be influenced by dissolution of mineral assemblages associated with ore deposits that are present along the basin margins. Ground-water ages, dissolved-solids concentrations, and calcium-strontium concentrations indicate limited or partial connectivity between fractures and contributions of uncontaminated recharge water downgradient from the site that dilutes contaminant concentrations. Changes in RDX and nitrate concentration patterns, the presence of methane, changes in carbon dioxide concentrations and d15N and d34S values, and variable reduction-oxidation conditions suggest degradation of contaminants in the downgradient direction. Estimated values of electron potential were assigned to ground water collected in October 2005 from all monitoring sites at the Hazardous Test Area. Moderate to strong reducing conditions were present upgradient from the Open Burn/Open Detonation site, at the site, and at various locations downgradient from the site, but the aquifer contained well-oxygenated water between many of the reducing areas. The spatial variability of reduction-oxidation conditions in the aquifer exemplifies the partial connectivity of the fracture system(s). Dilution of the contaminants i

New Mexico↗