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Groundwater quality and geochemistry of West Virginia’s southern coal fields

Coal mining has been the dominant industry and land use in West Virginia’s southern coal fields since the mid-1800s. Mortality rates for a variety of serious chronic conditions, such as diabetes, heart disease, and some forms of cancer in Appalachian coal mining regions, are higher than in areas lacking substantial coal mining activity within the Appalachian Region or elsewhere in the United States. Causes of the increased mortality and morbidity are not clear, but poor diet, high rates of smoking, socioeconomic factors, and the quality of groundwater used by area residents are all possible contributing factors. This study was conducted by the U.S. Geological Survey in cooperation with the West Virginia Department of Health and Human Resources and the West Virginia Department of Environmental Protection, with grant support from the Centers for Disease Control and Prevention (CDC) to assess the quality of groundwater in southern West Virginia. The data from this assessment of groundwater quality may be used by the CDC and other agencies to potentially investigate the role or lack thereof of groundwater quality with respect to mortality and morbidity rates in the region. The study was conducted in a region where a high density of current or past coal mining combined with a lack of advanced sewage treatment could affect concentrations of commonly occurring constituents plus contaminants, including nitrate, trace metals, major ions, indicator bacteria, radon, hydrogen sulfide, and dissolved hydrocarbons. Because rural residential wells and mine outfalls are considered private sources of water in the region, and are therefore unregulated and unmonitored, water-quality data are sparse. To fill the data gap and assess the groundwater quality in the region, water-quality samples were collected from 60 sites in a 10-county area. The 60 sites sampled included 46 rural residential homeowner wells and 14 mine outfall discharges used for residential supply. For this study, all samples were collected prior to any filtration or other treatments, typically at the pressure tank, and are indicative of total and dissolved constituents in the untreated water. Generally, data for the 60 sites indicate that most waters sampled do not exceed thresholds for most U.S. Environmental Protection Agency (EPA) drinking-water standards and U.S. Geological Survey (USGS) drinking-water screening criteria. However, there were several notable exceptions. Turbidity exceeded the 5-Nephelometric Turbidity Unit (NTU) EPA treatment technique (TT) drinking-water standard in 14 of 60 (23 percent) sites sampled and exceeded the 1-NTU TT standard in 51 of 60 (85 percent) sites sampled. Turbidity is common in many wells in southern West Virginia and may be attributed to iron oxyhydroxide precipitates, sediment carried into the aquifers from the shallow soil zone due to improperly constructed or cased wells or transported to the aquifer in shallow stress-relief fracture zones or through permeable bedding-plane partings. For the sites sampled, 31 of 60 (52 percent) had pH values at, above, or below the upper and lower range of the EPA Secondary Maximum Contaminant Level (SMCL, 6.5–8.5 standard units). Of those 31 sites, 28 (90 percent) were indicative of acidic corrosive water and 3 (10 percent) were indicative of alkaline water. The Langelier Saturation Index (LSI), which is a measure of the corrosivity of the water, was computed for all sites sampled for the study. Eighty-two percent of the sites sampled had waters that were classified as corrosive, based on a LSI less than −0.5. Corrosive water has the potential to leach lead, copper, and other metals from lead, copper, galvanized, or lead-tin soldered connections in water lines. The chloride to sulfate mass ratio also was assessed with the alkalinity to indicate the potential to promote galvanic corrosion (PPGC) of water lines and plumbing fixtures. Only one of the sites (1.7 percent) classified as a corrosive water site, had a PPGC considered high; the remaining sites were classified as having either a moderate (53.3 percent) or low (45 percent) PPGC. Therefore, the type of plumbing systems sampled for this study may be affected by corrosive water, but the potential for leaching trace metals and other constituents from residential plumbing systems containing older galvanized pipes or lead-tin soldered copper pipes is moderate to low. The indicator bacteria total coliform and Escherichia coli ( E. coli ) also were detected in groundwater samples to varying degrees. Total coliforms, which are a broad class of indicator bacteria, are common in groundwater in southern West Virginia and were detected in 39 of the 60 sites (65 percent) sampled. The presence of total coliform bacteria is a potential indicator of surface contamination, due to improperly constructed or cased wells, or infiltration of soil or other surface contaminants into the aquifer or well bore. E. coli bacteria, however, are much more indicative of fecal contamination of groundwater from either human or animal sources, and 14 of the 60 (23 percent) sites sampled had detections of E. coli . Although only a few strains of E. coli are known pathogens, their presence in groundwater may be an indicator of other related pathogens such as viruses and should be regarded as a serious potential issue. Water treatment such as chlorination, ozonation, or ultraviolet light may be appropriate to kill potential pathogenic bacteria or viruses in the source water. Manganese and iron were prevalent contaminants in the groundwater samples collected for this study, with 30 of 60 (50 percent) sites analyzed for manganese and 25 of 60 (42 percent) sites analyzed for iron exceeding the proposed 50- and 300-micrograms per liter (µg/L) SMCL drinking-water standards, respectively, for aesthetic criteria such as taste, odor, or staining of plumbing fixtures. Fourteen of the 60 sites sampled (23 percent) had concentrations of manganese that exceeded the 300-µg/L USGS health-based screening level, and 1 site exceeded the 1,600-µg/L EPA drinking-water equivalent level, which is based on a lifetime exposure level. Sodium is another common constituent in groundwater within the study area. Sodium has an EPA health-based value (HBV) of 20 milligrams per liter (mg/L) for individuals who are on a sodium-restricted diet for blood pressure or other health reasons. Sodium concentrations exceeded the 20-mg/L EPA HBV in 27 of 60 (45 percent) samples. Radon, a naturally occurring carcinogenic radioactive gas known to cause lung cancer, was detected at concentrations at or exceeding the proposed 300-picocuries per liter (pCi/L) EPA Maximum Contaminant Level (MCL) in 12 of the 60 (20 percent) sites sampled. Sites with radon gas concentrations exceeding the 300-pCi/L proposed MCL have the potential for airborne concentrations of radon to exceed the 4-pCi/L indoor air standard. Inhalation of radon can cause lung cancer, and the 4-pCi/L indoor air standard is based on an inhalation standard. Therefore, homeowners whose wells have radon gas concentrations exceeding 300 pCi/L may be advised to have their indoor air tested to determine if indoor air concentrations exceed the 4-pCi/L indoor air standard established by the EPA. Various factors were analyzed statistically and graphically to determine whether they have an influence on groundwater quality within the study area, including topographic setting, well depth, type of mining (surface or underground), type of site (well or mine outfall), and geologic formation. Only geologic formation and the type of site sampled had strong statistical correlations with one or more of the constituents of concern for this study. The overall chemistry of outfalls (mine outfalls) and wells was significantly different, with a much higher dissolved oxygen content in outfalls than in wells. The dissolved oxygen content is the primary component driving the oxidation and reduction of minerals, and the precipitation of minerals that are saturated or super saturated with respect to various cations and anions. Median dissolved oxygen concentrations for the outfalls sampled was 8.75 mg/L, and only 0.4 mg/L for the wells sampled. Median concentrations of sulfate and selenium were much higher in waters from the outfalls sampled, with median concentrations of 73.75 mg/L and 2.35 µg/L, respectively, compared to the wells sampled, which had median concentrations of 18.3 mg/L and less than (<) the 0.05-µg/L method detection limit, respectively. The maximum selenium concentration was for a well, with a concentration of 16.6 µg/L. The geochemical processes that control sulfate and selenium concentrations in groundwater are similar and are the result of the oxidation of sulfide minerals such as pyrite and ferroselite. Iron and manganese concentrations were elevated in most of the wells sampled, with median concentrations of 269.5 and 124.5 µg/L, respectively, but were rarely detected in the outfalls sampled, with median concentrations of < 4.0 and < 0.4 µg/L, respectively. The difference in iron and manganese between wells and outfalls is indicative of the role of dissolved oxygen on processes controlling groundwater chemistry in the region. Three principal geologic formations were assessed for the study, and the overall chemistry for the Pocahontas, New River, and Kanawha Formations varied substantially with respect to several constituents. Concentrations of calcium, magnesium, and total dissolved solids were highest for sites sampled in the Pocahontas Formation, with median concentrations of 41.9, 18.6, and 312 mg/L, respectively. For constituents that are commonly associated with mining activity, the highest concentrations were for sites sampled in the New River Formation, with median concentrations of iron and manganese of 2,450 µg/L and 482 µg/L, respectively, and a median pH of 6.35 standard units. Concentrations of barium also were elevated in samples collected from sites in the New River Formation, with a median barium concentration of 184 µg/L. The source of the barium is not fully known but may be associated with commingling of shallow groundwater with deeper brines or dissolution of the mineral barite. The highest median sulfate concentrations were from sites sampled in the Pocahontas Formation, with a median concentration of 64.0 mg/L. Of the 12 sites at or exceeding the 300-pCi/L proposed drinking-water standard for radon, 8 (67 percent of MCL exceedances) were for sites deriving water from the Kanawha Formation, 3 (25 percent of MCL exceedances) were for sites deriving water from the New River Formation, and only 1 site was for water from the Pocahontas Formation (8 percent of proposed MCL exceedances). Dissolved hydrocarbons, including methane, ethane, propane, propene, n - and i -butane, 1-butene, n - and i -pentane, pentane, 2- and 3-ethyl pentane, hexane, and benzene were analyzed in samples collected from 59 of the 60 sites to assess the potential occurrence and sources of these trace gases in groundwater within the study area. Results of the analysis indicate that most of the gas is of shallow biogenic origin, possibly associated with coal-bed methane, but a subset of samples has a gas signature and a chloride to bromide ratio indicative of potential mixing with deeper thermogenic gases. Only 2 of the 59 (3.3 percent) sites sampled had concentrations of methane gas, which is a highly combustible and explosive gas, exceeding the 10 milligrams per kilogram level of concern established by the U.S. Office of Surface Mining Reclamation and Enforcement. Principal components analysis was used to assess the primary geochemical processes occurring in the aquifers sampled. The first principal component had significant positive loadings for bromide, chloride, silica, ammonia, barium, iron, manganese, and arsenic, and significant negative loadings for dissolved oxygen, potassium, nitrate, and uranium, and reflects reduction and oxidation (redox) processes occurring in deeper anoxic groundwater or shallow oxic groundwater. The strong positive loadings for iron, manganese, barium, and arsenic are correlated with reducing conditions often found deeper in the aquifer. More oxic water is correlated with oxidation of nitrogen species to nitrate and environmental mobilization of uranium and sulfate in shallow wells and mine outfalls.

West Virginia↗

Effects of human-induced alteration of groundwater flow on concentrations of naturally-occurring trace elements at water-supply wells

The effects of human-induced alteration of groundwater flow patterns on concentrations of naturally-occurring trace elements were examined in five hydrologically distinct aquifer systems in the USA. Although naturally occurring, these trace elements can exceed concentrations that are considered harmful to human health. The results show that pumping-induced hydraulic gradient changes and artificial connection of aquifers by well screens can mix chemically distinct groundwater. Chemical reactions between these mixed groundwaters and solid aquifer materials can result in the mobilization of trace elements such as U, As and Ra, with subsequent transport to water-supply wells. For example, in the High Plains aquifer near York, Nebraska, mixing of shallow, oxygenated, lower-pH water from an unconfined aquifer with deeper, confined, anoxic, higher-pH water is facilitated by wells screened across both aquifers. The resulting higher-O2, lower-pH mixed groundwater facilitated the mobilization of U from solid aquifer materials, and dissolved U concentrations were observed to increase significantly in nearby supply wells. Similar instances of trace element mobilization due to human-induced mixing of groundwaters were documented in: (1) the Floridan aquifer system near Tampa, Florida (As and U), (2) Paleozoic sedimentary aquifers in eastern Wisconsin (As), (3) the basin-fill aquifer underlying the California Central Valley near Modesto (U), and (4) Coastal Plain aquifers of New Jersey (Ra). Adverse water-quality impacts attributed to human activities are commonly assumed to be related solely to the release of the various anthropogenic contaminants to the environment. The results show that human activities including various land uses, well drilling, and pumping rates and volumes can adversely impact the quality of water in supply wells, when associated with naturally-occurring trace elements in aquifer materials. This occurs by causing subtle but significant changes in geochemistry and associated trace element mobilization as well as enhancing advective transport processes.

Applied Geochemistry↗

Groundwater availability in the Atlantic Coastal Plain of North and South Carolina

The Atlantic Coastal Plain aquifers and confining units of North and South Carolina are composed of crystalline carbonate rocks, sand, clay, silt, and gravel and contain large volumes of high-quality groundwater. The aquifers have a long history of use dating back to the earliest days of European settlement in the late 1600s. Although extensive areas of some of the aquifers have or currently (2009) are areas of groundwater level declines from large-scale, concentrated pumping centers, large areas of the Atlantic Coastal Plain contain substantial quantities of high-quality groundwater that currently (2009) are unused. Groundwater use from the Atlantic Coastal Plain aquifers in North Carolina and South Carolina has increased during the past 60 years as the population has increased along with demands for municipal, industrial, and agricultural water needs. While North Carolina and South Carolina work to increase development of water supplies in response to the rapid growth in these coastal populations, both States recognize that they are facing a number of unanswered questions regarding availability of groundwater supplies and the best methods to manage these important supplies. An in-depth assessment of groundwater availability of the Atlantic Coastal Plain aquifers of North and South Carolina has been completed by the U.S. Geological Survey Groundwater Resources Program. This assessment includes (1) a determination of the present status of the Atlantic Coastal Plain groundwater resources; (2) an explanation for how these resources have changed over time; and (3) development of tools to assess the system's response to stresses from potential future climate variability. Results from numerous previous investigations of the Atlantic Coastal Plain by Federal and State agencies have been incorporated into this effort. The primary products of this effort are (1) comprehensive hydrologic datasets such as groundwater levels, groundwater use, and aquifer properties; (2) a revised hydrogeologic framework; (3) simulated water budgets of the overall study area along with several subareas; and (4) construction and calibration of a numerical modeling tool that is used to forecast the potential effects of climate change on groundwater levels.

North Carolina, South Carolina↗

Regional potentiometric surface of the Ozark aquifer in Arkansas, Kansas, Missouri, and Oklahoma, November 2014–January 2015

The Ozark aquifer, within the Ozark Plateaus aquifer system (herein referred to as the &ldquo;Ozark system&rdquo;), is the primary groundwater source in the Ozark Plateaus physiographic province (herein referred to as the &ldquo;Ozark Plateaus&rdquo;) of Arkansas, Kansas, Missouri, and Oklahoma. Groundwater from the Ozark system has historically been an important part of the water resource base, and groundwater availability is a concern in some areas; dependency on the Ozark aquifer as a water supply has caused evolving, localized issues. The construction of a regional potentiometric-surface map of the Ozark aquifer is needed to aid assessment of current and future groundwater use and availability. The regional potentiometric-surface mapping is part of the U.S. Geological Survey (USGS) Groundwater Resources Program initiative ( http://water.usgs.gov/ogw/gwrp/activities/regional.html ) and the Ozark system groundwater availability project ( http://ar.water.usgs.gov/ozarks ), which seeks to quantify current groundwater resources, evaluate changes in these resources over time, and provide the information needed to simulate system response to future human-related and environmental stresses. The Ozark groundwater availability project objectives include assessing (1) growing demands for groundwater and associated declines in groundwater levels as agricultural, industrial, and public supply pumping increases to address needs; (2) regional climate variability and pumping effects on groundwater and surface-water flow paths; (3) effects of a gradual shift to a greater surface-water dependence in some areas; and (4) shale-gas production requiring groundwater and surface water for hydraulic fracturing. Data compiled and used to construct the regional Ozark aquifer potentiometric surface will aid in the assessment of those objectives.

Arkansas, Kansas, Missouri, Oklahoma↗

Water levels in the aquifers of the Nacatoch Sand of southwestern and northeastern Arkansas and the Tokio Formation of southwestern Arkansas, February–March 2011

The aquifers in the Nacatoch Sand and Tokio Formation in southwestern Arkansas and the Nacatoch Sand in northeastern Arkansas are sources of water for industrial, public supply, domestic, and agricultural uses. Potentiometric-surface maps were constructed from water-level measurements made in 47 wells completed in the Nacatoch Sand and 45 wells completed in the Tokio Formation during February and March 2011. Aquifers in the Nacatoch Sand and Tokio Formation are hereafter referred to as the Nacatoch aquifer and the Tokio aquifer, respectively. The direction of groundwater flow in the Nacatoch aquifer in southwestern Arkansas is towards the southeast in Hempstead, Little River, and Miller Counties and east-southeast in Clark and Nevada Counties. A potentiometric high is located within the outcrop area of north-central Hempstead County. Two cones of depression exist in the Nacatoch aquifer, one at Hope in southeastern Hempstead County and one in Clark County. The direction of groundwater flow in the Nacatoch aquifer in northeastern Arkansas generally is towards the southeast. A potentiometric high in the study area is located along the north and northwestern boundaries of the area, but water levels may be higher outside the study area. In northeastern Arkansas, groundwater withdrawals from the Nacatoch aquifer increased by 564 percent from 1965 to 2010. In southwestern Arkansas, groundwater withdrawals from the Nacatoch Sand increased by 125 percent from 1965 to 1980, and withdrawals decreased by 85 percent from 1980 to 2010. In southwestern Arkansas, groundwater withdrawals from the Tokio aquifer increased by 201 percent from 1965 to 1980, and withdrawals decreased by 81 percent from 1980 to 2000. Withdrawals from the Tokio aquifer increased by 291 percent from 2000 to 2005, and withdrawals decreased by 32 percent from 2005 to 2010. The direction of groundwater flow in the Tokio aquifer in southwestern Arkansas generally is towards the south or southeast. The potentiometric high is within the outcrop area in the northern part of the area. Artesian flow exists or is inferred in southeastern Pike, northeastern Hempstead, and northwestern Nevada Counties. One apparent cone of depression might exist northwest of Hope in Hempstead County.

Arkansas↗

Preliminary machine learning models of manganese and 1,4-dioxane in groundwater on Long Island, New York

Manganese and 1,4-dioxane in groundwater underlying Long Island, New York, were modeled with machine learning methods to demonstrate the use of these methods for mapping contaminants in groundwater in the Long Island aquifer system. XGBoost, a gradient boosted, ensemble tree method, was applied to data from 910 wells for manganese and 553 wells for 1,4-dioxane. Explanatory variables included soil properties, groundwater flow, land use, and other features that describe the hydrogeology and geochemistry of the aquifer system. Four models were developed to predict the probability of manganese concentrations greater than a detection level of 10 micrograms per liter (μg/L) and greater than three threshold concentrations (50, 150, and 300 μg/L) relevant to drinking-water quality. One model was developed to predict the probability of 1,4-dioxane concentrations greater than a detection level of 0.07 μg/L. The 1,4-dioxane model was limited geographically to Suffolk County because of data availability. Predictions were made for two layers in the upper glacial aquifer and three layers in the Magothy aquifer, which are the upper two of the three major aquifers of the Long Island aquifer system. The objective of the study described in this report was to demonstrate the application of the methods rather than to develop precise estimates of manganese or 1,4-dioxane concentrations at any given location. The predictive models developed in the study are considered preliminary in the sense that they are an initial effort at developing these kinds of models specifically for Long Island. The models could be improved by the inclusion of additional data, by the use of methods to improve the modeling of infrequent high concentrations of manganese and 1,4-dioxane (above threshold concentrations), and by including more explanatory variables that specifically describe conditions and contaminant sources on Long Island. Nonetheless, the distribution of model predictions and the influence of explanatory variables in the models were consistent with the expected relations between contaminant concentrations and groundwater-flow-system characteristics and the distribution of manmade sources. Mapped predictions indicated that manganese detections were more probable in the upper glacial aquifer and along the southern shore of Long Island, consistent with the distribution of anoxic conditions in groundwater in the Long Island aquifer system. Manganese was infrequently predicted at concentrations greater than thresholds of concern for drinking-water quality in any of the aquifer layers. Detections of 1,4-dioxane were predicted in the western, more highly developed parts of Suffolk County, in the upper glacial aquifer and the top and middle layers of the Magothy aquifer, and in northwestern Suffolk County in the bottom layer of the Magothy aquifer. Although preliminary in nature and based on limited data, these mapped predictions can be used to generally identify areas where manganese and 1,4-dioxane may be present at concentrations of concern to prioritize areas for future monitoring and to guide future modeling and mapping efforts.

New York↗

Groundwater-quality data in the Borrego Valley, Central Desert, and Low-Use Basins of the Mojave and Sonoran Deserts study unit, 2008-2010--Results from the California GAMA Program

Groundwater quality in the 12,103-square-mile Borrego Valley, Central Desert, and Low-Use Basins of the Mojave and Sonoran Deserts (CLUB) study unit was investigated by the U.S. Geological Survey (USGS) from December 2008 to March 2010, as part of the California State Water Resources Control Board (SWRCB) Groundwater Ambient Monitoring and Assessment (GAMA) Program's Priority Basin Project (PBP). The GAMA-PBP was developed in response to the California Groundwater Quality Monitoring Act of 2001 and is being conducted in collaboration with the SWRCB and Lawrence Livermore National Laboratory (LLNL). The CLUB study unit was the twenty-eighth study unit to be sampled as part of the GAMA-PBP. The GAMA CLUB study was designed to provide a spatially unbiased assessment of untreated-groundwater quality in the primary aquifer systems, and to facilitate statistically consistent comparisons of untreated-groundwater quality throughout California. The primary aquifer systems (hereinafter referred to as primary aquifers) are defined as parts of aquifers corresponding to the perforation intervals of wells listed in the California Department of Public Health (CDPH) database for the CLUB study unit. The quality of groundwater in shallow or deep water-bearing zones may differ from the quality of groundwater in the primary aquifers; shallow groundwater may be more vulnerable to surficial contamination. In the CLUB study unit, groundwater samples were collected from 52 wells in 3 study areas (Borrego Valley, Central Desert, and Low-Use Basins of the Mojave and Sonoran Deserts) in San Bernardino, Riverside, Kern, San Diego, and Imperial Counties. Forty-nine of the wells were selected by using a spatially distributed, randomized grid-based method to provide statistical representation of the study unit (grid wells), and three wells were selected to aid in evaluation of water-quality issues (understanding wells). The groundwater samples were analyzed for organic constituents (volatile organic compounds [VOCs], pesticides and pesticide degradates, and pharmaceutical compounds), constituents of special interest (perchlorate and N -nitrosodimethylamine [NDMA]), naturally-occurring inorganic constituents (trace elements, nutrients, major and minor ions, silica, total dissolved solids [TDS], alkalinity, and species of inorganic chromium), and radioactive constituents (radon-222, radium isotopes, and gross alpha and gross beta radioactivity). Naturally-occurring isotopes (stable isotopes of hydrogen, oxygen, boron, and strontium in water, stable isotopes of carbon in dissolved inorganic carbon, activities of tritium, and carbon-14 abundance) and dissolved noble gases also were measured to help identify the sources and ages of sampled groundwater. In total, 223 constituents and 12 water-quality indicators were investigated. Three types of quality-control samples (blanks, replicates, and matrix spikes) were collected at up to 10 percent of the wells in the CLUB study unit, and the results for 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 contamination from sample collection procedures was not a significant source of bias in the data for the groundwater samples. Replicate samples generally were within the limits of acceptable analytical reproducibility. Median matrix-spike recoveries were within the acceptable range (70 to 130 percent) for approximately 85 percent of the compounds. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, untreated groundwater typically is treated, disinfected, and (or) blended with other waters to maintain water quality. Regulatory benchmarks apply to water that is delivered to the consumer, not to untreated groundwater. However, to provide some context for the results, concentrations of constituents measured in the untreated groundwater were compared with regulatory and non-regulatory health-based benchmarks established by the U.S. Environmental Protection Agency (USEPA) and CDPH, and to non-regulatory benchmarks established for aesthetic concerns by CDPH. Comparisons between data collected for this study and benchmarks for drinking water are for illustrative purposes only and are not indicative of compliance or non-compliance with those benchmarks. Most inorganic constituents detected in groundwater samples from the 49 grid wells were detected at concentrations less than drinking-water benchmarks. In addition, all detections of organic constituents from the CLUB study-unit grid-well samples were less than health-based benchmarks. In total, VOCs were detected in 17 of the 49 grid wells sampled (approximately 35 percent), pesticides and pesticide degradates were detected in 5 of the 47 grid wells sampled (approximately 11 percent), and perchlorate was detected in 41 of 49 grid wells sampled (approximately 84 percent). Trace elements, major and minor ions, and nutrients were sampled for at 39 grid wells, and radioactive constituents were sampled for at 23 grid wells; most detected concentrations were less than health-based benchmarks. Exceptions in the grid-well samples include seven detections of arsenic greater than the USEPA maximum contaminant level (MCL-US) of 10 micrograms per liter (&mu;g/L); four detections of boron greater than the CDPH notification level (NL-CA) of 1,000 &mu;g/L; six detections of molybdenum greater than the USEPA lifetime health advisory level (HAL-US) of 40 &mu;g/L; two detections of uranium greater than the MCL-US of 30 &mu;g/L; nine detections of fluoride greater than the CDPH maximum contaminant level (MCL-CA) of 2 milligrams per liter (mg/L); one detection of nitrite plus nitrate (NO 2- +NO 3- ), as nitrogen, greater than the MCL-US of 10 mg/L; and four detections of gross alpha radioactivity (72-hour count), and one detection of gross alpha radioactivity (30-day count), greater than the MCL-US of 15 picocuries per liter. Results for constituents with non-regulatory benchmarks set for aesthetic concerns showed that a manganese concentration greater than the CDPH secondary maximum contaminant level (SMCL-CA) of 50 &mu;g/L was detected in one grid well. Chloride concentrations greater than the recommended SMCL-CA benchmark of 250 mg/L were detected in three grid wells, and one of these wells also had a concentration that was greater than the upper SMCL-CA benchmark of 500 mg/L. Sulfate concentrations greater than the recommended SMCL-CA benchmark of 250 mg/L were measured in six grid wells. TDS concentrations greater than the SMCL-CA recommended benchmark of 500 mg/L were measured in 20 grid wells, and concentrations in 2 of these wells also were greater than the SMCL-CA upper benchmark of 1,000 mg/L.

California↗

Groundwater-quality data in the Western San Joaquin Valley study unit, 2010 - Results from the California GAMA Program

Groundwater quality in the approximately 2,170-square-mile Western San Joaquin Valley (WSJV) study unit was investigated by the U.S. Geological Survey (USGS) from March to July 2010, as part of the California State Water Resources Control Board (SWRCB) Groundwater Ambient Monitoring and Assessment (GAMA) Program's Priority Basin Project (PBP). The GAMA-PBP was developed in response to the California Groundwater Quality Monitoring Act of 2001 and is being conducted in collaboration with the SWRCB and Lawrence Livermore National Laboratory (LLNL). The WSJV study unit was the twenty-ninth study unit to be sampled as part of the GAMA-PBP. The GAMA Western San Joaquin Valley study was designed to provide a spatially unbiased assessment of untreated-groundwater quality in the primary aquifer system, and to facilitate statistically consistent comparisons of untreated groundwater quality throughout California. The primary aquifer system is defined as parts of aquifers corresponding to the perforation intervals of wells listed in the California Department of Public Health (CDPH) database for the WSJV study unit. Groundwater quality in the primary aquifer system may differ from the quality in the shallower or deeper water-bearing zones; shallow groundwater may be more vulnerable to surficial contamination. In the WSJV study unit, groundwater samples were collected from 58 wells in 2 study areas (Delta-Mendota subbasin and Westside subbasin) in Stanislaus, Merced, Madera, Fresno, and Kings Counties. Thirty-nine of the wells were selected by using a spatially distributed, randomized grid-based method to provide statistical representation of the study unit (grid wells), and 19 wells were selected to aid in the understanding of aquifer-system flow and related groundwater-quality issues (understanding wells). The groundwater samples were analyzed for organic constituents (volatile organic compounds [VOCs], low-level fumigants, and 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 (trace elements, nutrients, dissolved organic carbon [DOC], major and minor ions, silica, total dissolved solids [TDS], alkalinity, total arsenic and iron [unfiltered] and arsenic, chromium, and iron species [filtered]). Isotopic tracers (stable isotopes of hydrogen, oxygen, and boron in water, stable isotopes of nitrogen and oxygen in dissolved nitrate, stable isotopes of sulfur in dissolved sulfate, isotopic ratios of strontium in water, stable isotopes of carbon in dissolved inorganic carbon, activities of tritium, and carbon-14 abundance), dissolved standard gases (methane, carbon dioxide, nitrogen, oxygen, and argon), and dissolved noble gases (argon, helium-4, krypton, neon, and xenon) were measured to help identify sources and ages of sampled groundwater. In total, 245 constituents and 8 water-quality indicators were measured. Quality-control samples (blanks, replicates, or matrix spikes) were collected at 16 percent of the wells in the WSJV study unit, and the results for these samples were used to evaluate the quality of the data from the groundwater samples. Blanks rarely contained detectable concentrations of any constituent, suggesting that contamination from sample collection procedures was not a significant source of bias in the data for the groundwater samples. Replicate samples all were within acceptable limits of variability. Matrix-spike recoveries were within the acceptable range (70 to 130 percent) for approximately 87 percent of the compounds. This study did not evaluate the quality of water delivered to consumers. After withdrawal, groundwater typically is treated, disinfected, and (or) blended with other waters to maintain water quality. Regulatory benchmarks apply to water that is delivered to the consumer, not to untreated groundwater. However, to provide some context for the results, concentrations of constituents measured in the untreated groundwater were compared with regulatory and non-regulatory health-based benchmarks established by the U.S. Environmental Protection Agency (USEPA) and CDPH, and to non-regulatory benchmarks established for aesthetic concerns by CDPH. Comparisons between data collected for this study and benchmarks for drinking water are for illustrative purposes only and are not indicative of compliance or non-compliance with those benchmarks. Most inorganic constituents detected in groundwater samples from the 39 grid wells were detected at concentrations less than health-based benchmarks. Detections of organic and special-interest constituents from grid wells sampled in the WSJV study unit also were less than health-based benchmarks. In total, VOCs were detected in 12 of the 39 grid wells sampled (approximately 31 percent), pesticides and pesticide degradates were detected in 9 grid wells (approximately 23 percent), and perchlorate was detected in 15 grid wells (approximately 38 percent). Trace elements, major and minor ions, and nutrients were sampled for at 39 grid wells; most concentrations were less than health-based benchmarks. Exceptions include two detections of arsenic greater than the USEPA maximum contaminant level (MCL-US) of 10 micrograms per liter (&mu;g/L), 20 detections of boron greater than the CDPH notification level (NL-CA) of 1,000 &mu;g/L, 2 detections of molybdenum greater than the USEPA lifetime health advisory level (HAL-US) of 40 &mu;g/L, 1 detection of selenium greater than the MCL-US of 50 &mu;g/L, 2 detections of strontium greater than the HAL-US of 4,000 &mu;g/L, and 3 detections of nitrate greater than the MCL-US of 10 &mu;g/L. Results for inorganic constituents with non-health-based benchmarks (iron, manganese, chloride, sulfate, and TDS) showed that iron concentrations greater than the CDPH secondary maximum contaminant level (SMCL-CA) of 300 &mu;g/L were detected in five grid wells. Manganese concentrations greater than the SMCL-CA of 50 &mu;g/L were detected in 16 grid wells. Chloride concentrations greater than the recommended SMCL-CA benchmark of 250 milligrams per liter (mg/L) were detected in 14 grid wells, and concentrations in 5 of these wells also were greater than the upper SMCL-CA benchmark of 500 mg/L. Sulfate concentrations greater than the recommended SMCL-CA benchmark of 250 mg/L were measured in 21 grid wells, and concentrations in 13 of these wells also were greater than the SMCL-CA upper benchmark of 500 mg/L. TDS concentrations greater than the SMCL-CA recommended benchmark of 500 mg/L were measured in 36 grid wells, and concentrations in 20 of these wells also were greater than the SMCL-CA upper benchmark of 1,000 mg/L.

California↗

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&ndash;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 &ldquo;Bexar County index well&rdquo;) 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↗

Hydrogeology and hydrologic conditions of the Ozark Plateaus aquifer system

The hydrogeology and hydrologic characteristics of the Ozark Plateaus aquifer system were characterized as part of ongoing U.S. Geological Survey efforts to assess groundwater availability across the Nation. The need for such a study in the Ozark Plateaus physiographic province (Ozark Plateaus) is highlighted by increasing demand on groundwater resources by the 5.3 million people of the Ozark Plateaus, water-level declines in some areas, and potential impacts of climate change on groundwater availability. The subject study integrates knowledge gained through local investigation within a regional perspective to develop a regional conceptual model of groundwater flow in the Ozark Plateaus aquifer system (Ozark system), a key phase of groundwater availability assessment. The Ozark system extends across much of southern Missouri and northwestern and north-central Arkansas and smaller areas of southeastern Kansas and northeastern Oklahoma. The region is one of the major karst landscapes in the United States, and karst aquifers are predominant in the Ozark system. Groundwater flow is ultimately controlled by aquifer and confining unit lithologies and stratigraphic relations, geologic structure, karst development, and the character of surficial lithologies and regolith mantle. The regolith mantle is a defining element of Ozark Plateaus karst, affecting recharge, karst development, and vulnerability to surface-derived contaminants. Karst development is more advanced—as evidenced by larger springs, hydraulic characteristics, and higher well yields—in the Salem Plateau and in the northern part of the Springfield Plateau (generally north of the Arkansas-Missouri border) as compared with the southern part of the Springfield Plateau in Arkansas, largely due to thinner, less extensive regolith and purer carbonate lithology. Precipitation is the ultimate source of all water to the Ozark system, and the hydrologic budget for the Ozark system includes inputs from recharge, losing-stream sections, and groundwater inflows and losses of water to gaining-stream sections, groundwater withdrawals, and surface-water and groundwater outflows to neighboring systems. Groundwater recharge, estimated by a soil-water-balance model, represents about 24 percent, or 11 inches, of 43.9 inches annual precipitation. Recharge is spatially variable, being greater in the northern Springfield Plateau and Salem Plateau than in the southern Springfield Plateau (generally south of the Arkansas border) because of differences in regolith mantle extent and thickness and carbonate lithology and hydraulic properties. Increased precipitation and decreased agricultural land use during the period 1951 through 2011 increased recharge by approximately 5 percent. Although all Ozark streams have losing, neutral, and gaining sections, they are dominantly gaining and are a net sink for groundwater with nearly 90 percent of groundwater recharge returned to springs and streams. Groundwater pumping is a small but important loss of water in the Ozark system hydrologic budget; water-level declines and local cones of depression have been observed around pumping centers and strong concerns exist over potential effects on stream and spring flow. Data indicate that societal needs for freshwater resources in the Ozark Plateaus will continue to increase and will do so in the context of changing climate and hydrology. Groundwater will continue to be an important part of supporting these societal needs and also local ecosystems. The unique character and hydrogeologic variability across the Ozark system will control how the system responds to future stress. Groundwater of the Ozark system in the northern study area is more dynamic, has greater storage and larger flux, and has greater potential for further development than in the part of the study area south of the Arkansas-Missouri border. Further south in Arkansas, a line exists, roughly defined as 5 miles south of the Springfield Plateau-Boston Mountains boundary, beyond which further extensive municipal or commercial development appears unlikely under current economic and resource-need conditions. A small part of the Ozark system groundwater budget is currently drafted for use, leaving an apparently large component available for further development and use—particularly in the northern Springfield Plateau and Salem Plateau; however, the effects of increased pumping on groundwater’s role in maintaining ecosystems and ecosystem services are not quantitatively well understood, and the close relation between groundwater and surface water highlights the importance of further quantitative assessment.

Arkansas, Kansas, Missouri, Oklahoma↗

A novel high-frequency groundwater quality monitoring system

High-frequency, long-term monitoring of water quality has revolutionized the study of surface waters in recent years. However, application of these techniques to groundwater has been limited by the ability to remotely pump and analyze groundwater. This paper describes a novel autonomous groundwater quality monitoring system which samples multiple wells to evaluate temporal changes and identify trends in groundwater chemistry. The system, deployed near Fresno, California, USA, collects and transmits high-frequency data, including water temperature, specific conductance, pH, dissolved oxygen, and nitrate, from supply and monitoring wells, in real-time. The system consists of a water quality sonde and optical nitrate sensor, manifold, submersible three-phase pump, variable frequency drive, data collection platform, solar panels, and rechargeable battery bank. The manifold directs water from three wells to a single set of sensors, thereby reducing setup and operation costs associated with multi-sensor networks. Sampling multiple wells at high frequency for several years provided a means of monitoring the vertical distribution and transport of solutes in the aquifer. Initial results show short period variability of nitrate, specific conductivity, and dissolved oxygen in the shallow aquifer, while the deeper portion of the aquifer remains unchanged—observations that may be missed with traditional discrete sampling approaches. In this aquifer system, nitrate and specific conductance are increasing in the shallow aquifer, while invariant changes in deep groundwater chemistry likely reflect relatively slow groundwater flow. In contrast, systems with high groundwater velocity, such as karst aquifers, have been shown to exhibit higher-frequency groundwater chemistry changes. The stability of the deeper aquifer over the monitoring period was leveraged to develop estimates of measurement system uncertainty, which were typically lower than the manufacturer’s stated specifications, enabling the identification of subtle variability in water chemistry that may have otherwise been missed.

California↗

Hydrogeology and simulation of groundwater flow in fractured rock in the Newark basin, Rockland County, New York

Groundwater in the Newark basin aquifer flows primarily through discrete water-bearing zones parallel to the strike and dip of bedding, whereas flow perpendicular to the strike is restricted, thereby imparting anisotropy to the groundwater flow field. The finite-element model SUTRA was used to represent bedrock structure in the aquifer by spatially varying the orientation of the hydraulic conductivity tensor to reflect variations in the strike and dip of the bedding. Directions of maximum and medium hydraulic conductivity were oriented parallel to the bedding, and the direction of minimum hydraulic conductivity was oriented perpendicular to the bedding. Groundwater flow models were prepared to simulate local flow in the vicinity of the Spring Valley well field and regional flow through the Newark basin aquifer. The Newark basin contains sedimentary rocks deposited as alluvium during the Late Triassic and is one of a series of basins that developed when Mesozoic rifting of the super continent Pangea created the Atlantic Ocean. The westward-dipping basin is filled with interbedded facies of coarse-grained to fine-grained rocks that were intruded by diabase associated with Jurassic volcanism. The Newark basin aquifer is bounded to the north and east by the Palisades sill and to the west by the Ramapo Fault. Although the general dip of bedding is toward the fault, mapping of conglomerate beds indicates the rocks are folded into broad anticlines and synclines. An alternative, more uniform pattern of regional structure, based on interpolated strike and dip measurements from a number of sources, has also been proposed. Two groundwater flow models (A for the former type of bedrock structure and B for the latter type) were developed to represent these alternative depictions of bedrock structure. Transient simulations were calibrated to reproduce measured water-level recoveries in a 9.3 mi&sup2 area surrounding the Spring Valley well field during a 5-day aquifer test in 1992. The models represented a 330-ft thick rock mass divided vertically into 10 equally spaced layers and were calibrated through nonlinear regression. Results of model B best matched the observed water-level recoveries with an estimated hydraulic conductivity of 9.5 ft/day, specific storage of 7.6 x 10 -6 ft -1, and K max : K min anisotropy ratio (hydraulic conductivity parallel to bedding: perpendicular to bedding) of 72:1. Model error was 50 percent greater in model A because the assumed structure did not match the actual strike of bedding in this area. Steady-state simulations of regional flow through the 85.4-mi2 modeled extent of the Newark basin aquifer represented both the alluvial aquifer beneath the Mawah River and the fractured bedrock. The rock mass was divided into two aquifer units: an upper 500-ft thick unit divided into 10 equally spaced layers through which most groundwater is assumed to flow and a lower unit divided into 7 layers with increasing thickness. Models were calibrated through nonlinear regression to average water levels measured in 140 wells from August 2005 through April 2007. Water levels simulated using the two models were similar and generally matched those observed, and the average recharge rate estimated using both models was 19 inches/year for the simulated period. Estimated transmissivity parallel to the strike of bedding (1,100 ft&sup2/d) was uniform in two transmissivity (T) zones in model A, but in model B the transmissivity of a high T zone (1,600 ft&sup2/d), delineated on the basis of aquifer test data, was slightly greater than in a low T zone (1,300 ft&sup2/d). The K max : K min anisotropy was estimated to be 58:1 in model A and 410:1 in model B, so the proportion of flow perpendicular to bedding is less in model B than in model A. Distributions of groundwater age simulated with models A and B are similar and indicate that most shallow ground-water (225 ft below the bedrock surface) is 5 t

Scientific Investigations Report↗

Creating a monthly time series of the potentiometric surface in the Upper Floridan aquifer, Northern Tampa Bay area, Florida, January 2000-December 2009

In Florida’s karst terrain, where groundwater and surface waters interact, a mapping time series of the potentiometric surface in the Upper Floridan aquifer offers a versatile metric for assessing the hydrologic condition of both the aquifer and overlying streams and wetlands. Long-term groundwater monitoring data were used to generate a monthly time series of potentiometric surfaces in the Upper Floridan aquifer over a 573-square-mile area of west-central Florida between January 2000 and December 2009. Recorded groundwater elevations were collated for 260 groundwater monitoring wells in the Northern Tampa Bay area, and a continuous time series of daily observations was created for 197 of the wells by estimating missing daily values through regression relations with other monitoring wells. Kriging was used to interpolate the monthly average potentiometric-surface elevation in the Upper Floridan aquifer over a decade. The mapping time series gives spatial and temporal coherence to groundwater monitoring data collected continuously over the decade by three different organizations, but at various frequencies. Further, the mapping time series describes the potentiometric surface beneath parts of six regionally important stream watersheds and 11 municipal well fields that collectively withdraw about 90 million gallons per day from the Upper Floridan aquifer. Monthly semivariogram models were developed using monthly average groundwater levels at wells. Kriging was used to interpolate the monthly average potentiometric-surface elevations and to quantify the uncertainty in the interpolated elevations. Drawdown of the potentiometric surface within well fields was likely the cause of a characteristic decrease and then increase in the observed semivariance with increasing lag distance. This characteristic made use of the hole effect model appropriate for describing the monthly semivariograms and the interpolated surfaces. Spatial variance reflected in the monthly semivariograms decreased markedly between 2002 and 2003, timing that coincided with decreases in well-field pumping. Cross-validation results suggest that the kriging interpolation may smooth over the drawdown of the potentiometric surface near production wells. The groundwater monitoring network of 197 wells yielded an average kriging error in the potentiometric-surface elevations of 2 feet or less over approximately 70 percent of the map area. Additional data collection within the existing monitoring network of 260 wells and near selected well fields could reduce the error in individual months. Reducing the kriging error in other areas would require adding new monitoring wells. Potentiometric-surface elevations fluctuated by as much as 30 feet over the study period, and the spatially averaged elevation for the entire surface rose by about 2 feet over the decade. Monthly potentiometric-surface elevations describe the lateral groundwater flow patterns in the aquifer and are usable at a variety of spatial scales to describe vertical groundwater recharge and discharge conditions for overlying surface-water features.

Florida↗

Characterization of the structure, clean-sand percentage, dissolved-solids concentrations, and estimated quantity of groundwater in the Upper Cretaceous Nacatoch Sand and Tokio Formation, Arkansas

The West Gulf Coastal Plain, Mississippi embayment, and underlying Cretaceous aquifers are rich in water resources; however, large parts of the aquifers are largely unusable because of large concentrations of dissolved solids. Cretaceous aquifers are known to have large concentrations of salinity in some parts of Arkansas. The Nacatoch Sand and the Tokio Formation of Upper Cretaceous age were chosen for investigation because these aquifers produce groundwater to wells near their outcrops and have large salinity concentrations away from their outcrop areas. Previous investigations have indicated that dissolved-solids concentrations of groundwater within the Nacatoch Sand, 2–20 miles downdip from the outcrop, render the groundwater as unusable for purposes requiring freshwater. Groundwater within the Tokio Formation also exhibits large concentrations of dissolved solids downdip. Water-quality data showing elevated dissolved-solids concentrations are limited for these Cretaceous aquifers because other shallower aquifers are used for water supply. Although not suitable for many uses, large, unused amounts of saline groundwater are present in these aquifers. Historical borehole geophysical logs were used to determine the geologic and hydrogeologic properties of these Cretaceous aquifers, as well as the quality of the groundwater within the aquifers. Based on the interpretation of borehole geophysical logs, in Arkansas, the altitude of the top of the Nacatoch Sand ranges from more than 200 to less than -4,000 feet; the structural high occurs in the outcrop area and the structural low occurs in southeastern Arkansas near the Desha Basin structural feature. The thickness of the Nacatoch Sand ranges from 0 to over 550 feet. The minimum thickness occurs where the formation pinches out in the outcrop area, and the maximum thickness occurs in the southwestern corner of Arkansas. Other areas of large thickness include the area of the Desha Basin structural feature in southeastern Arkansas and in an area on the border of Cross and St. Francis Counties in eastern Arkansas. The clean-sand percentage of the total Nacatoch Sand thickness ranges from less than 20 percent to more than 60 percent and generally decreases downdip. The Nacatoch Sand contains more than 120.5 million acre-feet of water with a dissolved-solids concentration between 1,000 and 10,000 milligrams per liter (mg/L), more than 57.5 million acre-feet of water with a dissolved-solids concentration between 10,000 and 35,000 mg/L, and more than 122.5 million acre-feet of water with a dissolved-solids concentration more than 35,000 mg/L. The altitude of the top of the Tokio Formation, in Arkansas, ranges from more than 200 feet to less than -4,400 feet; the structural high occurs in the outcrop area and the structural low occurs in southeastern Arkansas near the Desha Basin structural feature. The thickness of the Tokio Formation, in Arkansas, ranges from 0 to over 400 feet. The minimum thickness occurs where the formation pinches out in the outcrop area, and the maximum thickness occurs in the southwestern corner of Arkansas. The clean-sand percentage of the total Tokio Formation thickness ranges from less than 20 percent to more than 60 percent and generally decreases away from the outcrop area. The Tokio Formation contains more than 2.5 million acre-feet of water with a dissolved-solids concentration between 1,000 and 10,000 mg/L, more than 12.5 million acre-feet of water with a dissolved-solids concentration between 10,000 and 35,000 mg/L, and nearly 43.5 million acre-feet of water with a dissolved-solids concentration more than 35,000 mg/L.

Arkansas↗

Lithology, hydrologic characteristics, and water quality of the Arkansas River Valley alluvial aquifer in the vicinity of Van Buren, Arkansas

A study to assess the potential of the Arkansas River Valley alluvial aquifer in the vicinity of Van Buren, Arkansas, as a viable source of public-supply water was conducted by the U.S. Geological Survey in cooperation with the Little Rock, District, U.S. Army Corps of Engineers. An important study component was to identify possible changes in hydrologic conditions following installation of James W. Trimble Lock and Dam 13 (December 1969) on the Arkansas River near the study area. Data were gathered for the study in regard to the lithology, hydrologic characteristics, and water quality of the aquifer. Lithologic information was obtained from drillers&rsquo; logs of wells drilled from 1957 through 1959. Water-quality samples were collected from 10 irrigation wells and analyzed for inorganic constituents and pesticides. To evaluate the potential viability of the alluvial aquifer in the Van Buren area, these data were compared to similar stratigraphic, lithologic, and groundwater-quality data from the Arkansas River Valley alluvial aquifer at Dardanelle, Ark., where the aquifer provides a proven, productive, sole-source of public-supply water. Drillers&rsquo; logs for 59 wells in the Van Buren study area revealed well depths ranging from 25 to 52 feet (ft), with a mean depth of 42 ft. The thickness of the lower sand/gravel interval serving as the water-producing zone ranged from 5 to 47 ft, with a mean thickness of 29 ft. The presence of gravel was noted in only 4 of 59 well logs available for review from the study area. Percent sand was calculated from well logs in the study area, and these sand percentages were overlain onto an orthophotograph map to examine the areal distribution of sand percentage in relation to geomorphologic features of the flood plain in the study area. The logs denoting the greatest percent sand tend to occur in areas near to the river and on the concave (point bar) side of abandoned channels, while the lower percent sand tends to occur on the convex (channel fill and backswamp deposits) side of the abandoned channels. Comparison of hydrographs from water levels collected between 1957 and 1972 to cumulative departure from mean monthly and mean annual precipitation showed overall good fit and explained the long-term decreasing water levels from the earliest period of record through October 1967, followed by a sharp rise in water levels concurrent with rises in cumulative departure from mean monthly and mean annual precipitation. Hydrographs for four wells ranging from 0.8 to 4.5 miles upstream from the dam and potentially affected by rising river stage were compared to graphs of river stage and cumulative departure from mean monthly precipitation. Water levels for these wells showed minimal discernible effect by rising river stage following dam completion. Periods of increased precipitation compared closely to increases in water level for all hydrographs, regardless of river stage, and periods of no precipitation resulted in declining water levels, although river stage continued to slowly rise during these same periods. The Arkansas River has greater salinity than local groundwater, providing a quantitative tracer for any groundwater recharge originating from the river. Comparison of predam and postdam groundwater-chloride concentrations showed no increase in chloride concentrations after dam installation, which is consistent with hydrologic data. These data suggest that the dominant source of groundwater recharge in the Arkansas River Valley alluvial aquifer is infiltration of precipitation through proximal, coarse channel deposits, with minimal influx of river water. Groundwater-quality data collected from 10 wells in the study area indicated a calcium-bicarbonate water type. No primary drinking-water standards were exceeded for any constituents, and iron and manganese were the only constituents exceeding secondary drinking-water regulations. Six of the 10 well-water samples were analyzed for the presence of pesticides, as row-crop agriculture is the dominant land use in the study area. Six herbicide compounds and one herbicide metabolite were detected at concentrations substantially below those of the Federal primary drinking-water standards and health advisories. The hydrologic and geochemical data gathered for this study provide a qualitative assessment of the potential of the Arkansas River Valley alluvial aquifer as a source of public water supply in the Van Buren area. Results indicate minimal influx of water from the Arkansas River, and recharge to the aquifer appears to be dominantly by infiltration of precipitation through overlying alluvium. If vertical wells are used as a source of public water supply, then several wells will have to be used in combination at relatively low pumping rates and placed in areas with a greater percent sand. Use of a horizontal well configuration near the river to increase production may depend on infiltration of river water to supplement water removed from storage, especially where areas of lower permeability sediments might be encountered within the surrounding alluvium. If a poor hydraulic connection exists between the river and the alluvium, as indicated by this study, then production will depend on ample precipitation and recharge throughout the year and groundwater storage sufficient to prevent declining water levels where pumping rates exceed recharge.

Arkansas↗

Development and application of a comprehensive simulation model to evaluate impacts of watershed structures and irrigation water use on streamflow and groundwater: The case of Wet Walnut Creek Watershed, Kansas, USA

This paper presents the results of a comprehensive modeling study of surface and groundwater systems, including stream-aquifer interactions, for the Wet Walnut Creek Watershed in west-central Kansas. The main objective of this study was to assess the impacts of watershed structures and irrigation water use on streamflow and groundwater levels, which in turn affect availability of water for the Cheyenne Bottoms Wildlife Refuge Management area. The surface-water flow model, POTYLDR, and the groundwater flow model, MODFLOW, were combined into an integrated, watershed-scale, continuous simulation model. Major revisions and enhancements were made to the POTYLDR and MODFLOW models for simulating the detailed hydrologic budget for the Wet Walnut Creek Watershed. The computer simulation model was calibrated and verified using historical streamflow records (at Albert and Nekoma gaging stations), reported irrigation water use, observed water-level elevations in watershed structure pools, and groundwater levels in the alluvial aquifer system. To assess the impact of watershed structures and irrigation water use on streamflow and groundwater levels, a number of hypothetical management scenarios were simulated under various operational criteria for watershed structures and different annual limits on water use for irrigation. A standard 'base case' was defined to allow comparative analysis of the results of different scenarios. The simulated streamflows showed that watershed structures decrease both streamflows and groundwater levels in the watershed. The amount of water used for irrigation has a substantial effect on the total simulated streamflow and groundwater levels, indicating that irrigation is a major budget item for managing water resources in the watershed. (C) 2000 Elsevier Science B.V.This paper presents the results of a comprehensive modeling study of surface and groundwater systems, including stream-aquifer interactions, for the Wet Walnut Creek Watershed in west-central Kansas. The main objective of this study was to assess the impacts of watershed structures and irrigation water use on streamflow and groundwater levels, which in turn affect availability of water for the Cheyenne Bottoms Wildlife Refuge Management area. The surface-water flow model, POTYLDR, and the groundwater flow model, MODFLOW, were combined into an integrated, watershed-scale, continuous simulation model. Major revisions and enhancements were made to the POTYLDR and MODFLOW models for simulating the detailed hydrologic budget for the Wet Walnut Creek Watershed. The computer simulation model was calibrated and verified using historical streamflow records (at Albert and Nekoma gaging stations), reported irrigation water use, observed water-level elevations in watershed structure pools, and groundwater levels in the alluvial aquifer system. To assess the impact of watershed structures and irrigation water use on streamflow and groundwater levels, a number of hypothetical management scenarios were simulated under various operational criteria for watershed structures and different annual limits on water use for irrigation. A standard `base case' was defined to allow comparative analysis of the results of different scenarios. The simulated streamflows showed that watershed structures decrease both streamflows and groundwater levels in the watershed. The amount of water used for irrigation has a substantial effect on the total simulated streamflow and groundwater levels, indicating that irrigation is a major budget item for managing water resources in the watershed.A comprehensive simulation model that combines the surface water flow model POTYLDR and the groundwater flow model MODFLOW was used to study the impacts of watershed structures (e.g., dams) and irrigation water use (including stream-aquifer interactions) on streamflow and groundwater. The model was revised, enhanced, calibrated, and verified, then applied to evaluate the hydrologic budget for Wet Wal

Journal of Hydrology↗

Environmental tracers of groundwater source, age, and geochemical evolution

Hexavalent chromium, Cr(VI), was discharged in cooling wastewater to unlined surface ponds from 1952 to 1964 and reached the underlying unconsolidated aquifer at the Pacific Gas and Electric Company (PG&E) Hinkley compressor station in the Mojave Desert, 80 miles northeast of Los Angeles, California. A suite of environmental tracers was analyzed in water samples collected from more than 100 wells to characterize the source, age, and geochemical evolution of groundwater within and near the Cr(VI) plume in Hinkley and Water Valleys. This information was used to help determine the extent of Cr(VI) associated with releases from the Hinkley compressor station and to identify Cr(VI) associated with natural sources. The source of water in most wells, indicated by stable oxygen and hydrogen isotope values for water, delta oxygen-18 and delta deuterium, was recharge by infiltration of intermittent surface flows in the Mojave River. With the exception of small flows in 1958, the Mojave River was largely dry between 1952 and 1969. This dry period spans the period of Cr(VI) releases from the Hinkley compressor station; 1952–69 also spans the period of high tritium levels in precipitation resulting from the atmospheric testing of nuclear weapons and, as a consequence, tritium concentrations in groundwater in Hinkley Valley were comparatively low. Groundwater ages (time since recharge) increased downgradient from the Mojave River and with depth. Tritium, measured by helium ingrowth with a study reporting level of 0.05 tritium unit, was detected in water from 51 percent of wells, with detectable tritium as far as 7 miles downgradient from the Mojave River. Tritium concentrations were higher, and tritium/helium-3 groundwater ages younger, in water from wells near the Mojave River and in water from shallower wells downgradient. Agricultural pumping has decreased groundwater levels as much as 60 feet since 1952. As a result of this pumping, some groundwater containing tritium, and presumably anthropogenic Cr(VI), has been removed from the aquifer. The distribution of wells having carbon-14 activities near or greater than 100-percent modern carbon, consistent with post-1952 recharge water, was similar to the distribution of wells containing detectable tritium. Carbon-14 activities as low as 8.9-percent modern carbon, with carbon-14 ages (unadjusted for reactions with aquifer materials) of almost 20,000 years before present (ybp), were sampled in water from some deep wells. Hexavalent chromium concentrations in older groundwater were as high as 11 micrograms per liter but did not exceed 3.6 micrograms per liter in older water from wells completed in “Mojave-type” deposits (composed of felsic Mojave River stream and near-shore lake deposits sourced from the Mojave River); this value may represent an upper limit on Cr(VI) concentrations in groundwater within Mojave-type deposits that likely approximates background Cr(VI) concentrations in the study area. Chlorofluorocarbons were released to the atmosphere and hydrologic cycle as a result of industrial activity beginning in the 1930s. Chlorofluorocarbon data were not generally suitable for groundwater-age dating in Hinkley and Water Valley because of nonatmospheric contributions from local sources. Strontium-87/86 isotope ratios and stable chromium isotopes, delta chromium-53, provide information on the geochemical evolution of groundwater in the aquifer. Highly radiogenic strontium-87/86 ratios greater than 0.71000 were present in water from wells completed in coarse-textured Mojave-type deposits having low chromium concentrations but were not diagnostic of these materials. Nonradiogenic strontium-87/86 ratios less than 0.70950 were diagnostic of weathered materials in the northern subarea of Hinkley and in Water Valley that were eroded from Miocene (23–5 million ybp) deposits east of the study area. Values for delta chromium-53 ranged from near 0 to 2.8 parts per thousand (‰) difference. The extent of reductive fractionation, mixing with native groundwater, and longitudinal dispersion within the October–December 2015 (Q4 2015) regulatory Cr(VI) plume can be estimated on the basis of the delta chromium-53 isotope composition of groundwater within the plume. Reduction of Cr(VI) to trivalent chromium, Cr(III), can occur in the presence of natural reductants in oxic groundwater. Although not diagnostic of anthropogenic chromium at the concentrations of interest near the Q4 2015 regulatory Cr(VI) plume margin, delta chromium-53 data indicate anthropogenic Cr(VI) within the plume is not conservative and has reacted with aquifer materials; these reactions have removed some anthropogenic Cr(VI) from groundwater. Environmental tracers, and the distribution of modern (post-1952) and premodern (pre-1952) groundwater, inform understanding of the extent of anthropogenic and naturally occurring Cr(VI) near the Q4 2015 regulatory Cr(VI) plume and the understanding of geochemical processes occurring in and near the margins of the Cr(VI) plume. The oxygen and hydrogen isotope compositions of water, tritium/helium-3 groundwater-age data, and carbon-14 data were used with mineralogy and chemistry data as part of a summative-scale analysis to determine the Cr(VI) plume extent later in this professional paper (chapter G).

California↗

Potentiometric Surfaces and Water-Level Trends in the Cockfield (Upper Claiborne) and Wilcox (Lower Wilcox) Aquifers of Southern and Northeastern Arkansas, 2009

Eocene-age sand beds near the base of the Cockfield Formation of Claiborne Group constitute the aquifer known locally as the Cockfield aquifer. Upper-Paleocene age sand beds within the lower parts of the Wilcox Group constitute the aquifer known locally as the Wilcox aquifer. In 2005, reported water withdrawals from the Cockfield aquifer in Arkansas totaled 16.1 million gallons per day, while reported water withdrawals from the Wilcox aquifer in Arkansas totaled 27.0 million gallons per day. Major withdrawals from these units were for industrial and public water supplies with lesser but locally important withdrawals for commercial, domestic, and agricultural uses. During February 2009, 56 water-level measurements were made in wells completed in the Cockfield aquifer and 57 water-level measurements were made in wells completed in the Wilcox aquifer. The results from the 2009 water-level measurements are presented in potentiometric-surface maps and in combination with previous water-level measurements. Trends in water-level change over time within the two aquifers are investigated using water-level difference maps and well hydrographs. Water-level difference maps were constructed for each aquifer using the difference between depth to water measurements made in 2003 to 2009. Well hydrographs for each aquifer were constructed for wells with 20 or more years of historical water-level data. The hydrographs were evaluated individually using linear regression to calculate the annual rise or decline in water levels, and by aggregating the regression results by county and statistically summarizing for the range, mean, and median water-level change in each county. The 2009 potentiometric surface of the Cockfield aquifer map indicates the regional direction of groundwater flow generally towards the east and southeast, except in two areas of intense groundwater withdrawals that have developed into cones of depression. The lowest water-level altitude measured was 43 feet and the highest water-level altitude measured was 351 feet. A water-level difference map was constructed from 54 wells completed in the Cockfield aquifer within Arkansas. The largest rise in water level was 14.9 feet and the largest decline was 27.4 feet. Seven wells had a rise in water level, and the remaining 47 wells had a decline in water level. Hydrographs for 33 wells completed in the Cockfield aquifer were developed. Hydrographs indicate water-level changes in individual wells ranged from rises of 0.33 feet per year to declines of 1.21 feet per year over the 20-year period (1990-2009). County summaries of the linear regression analysis indicate Cleveland and Columbia Counties have mean annual rises. Arkansas, Ashley, Bradley, Calhoun, Chicot, Desha, Drew, Lincoln, and Union Counties have mean annual declines. The potentiometric surface for the Wilcox aquifer is presented using two maps, one for a southern area and another for a northeastern area, because of the absence of water-level data in the central part of the State. The direction of groundwater flow in the southern area is generally the east, except around two cones of depression and around two mounds of elevated water levels. Water-level altitudes in the southern area range from 147 feet to 400 feet. The direction of groundwater flow in the northeastern area is generally to the south and southeast except in an area of intense groundwater withdrawals that has altered the flow to a westerly direction. Two water-level difference maps were constructed using water-level altitudes measured in 2003 to 2009 from 53 wells completed in the Wilcox aquifer within southern and northeastern Arkansas. In the southern area the largest rise in water level was 16.0 feet and the largest decline was 17.7 feet. Eight wells in the southern area had rising water levels and the remaining five wells had declining water levels. In the northeastern area, the largest rise in water level was 1.3 feet and the larg

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