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USGS2010

Steady-state and transient models of groundwater flow and advective transport, Eastern Snake River Plain aquifer, Idaho National Laboratory and vicinity, Idaho

Three-dimensional steady-state and transient models of groundwater flow and advective transport in the eastern Snake River Plain aquifer were developed by the U.S. Geological Survey in cooperation with the U.S. Department of Energy. The steady-state and transient flow models cover an area of 1,940 square miles that includes most of the 890 square miles of the Idaho National Laboratory (INL). A 50-year history of waste disposal at the INL has resulted in measurable concentrations of waste contaminants in the eastern Snake River Plain aquifer. Model results can be used in numerical simulations to evaluate the movement of contaminants in the aquifer. Saturated flow in the eastern Snake River Plain aquifer was simulated using the MODFLOW-2000 groundwater flow model. Steady-state flow was simulated to represent conditions in 1980 with average streamflow infiltration from 1966-80 for the Big Lost River, the major variable inflow to the system. The transient flow model simulates groundwater flow between 1980 and 1995, a period that included a 5-year wet cycle (1982-86) followed by an 8-year dry cycle (1987-94). Specified flows into or out of the active model grid define the conditions on all boundaries except the southwest (outflow) boundary, which is simulated with head-dependent flow. In the transient flow model, streamflow infiltration was the major stress, and was variable in time and location. The models were calibrated by adjusting aquifer hydraulic properties to match simulated and observed heads or head differences using the parameter-estimation program incorporated in MODFLOW-2000. Various summary, regression, and inferential statistics, in addition to comparisons of model properties and simulated head to measured properties and head, were used to evaluate the model calibration. Model parameters estimated for the steady-state calibration included hydraulic conductivity for seven of nine hydrogeologic zones and a global value of vertical anisotropy. Parameters estimated for the transient calibration included specific yield for five of the seven hydrogeologic zones. The zones represent five rock units and parts of four rock units with abundant interbedded sediment. All estimates of hydraulic conductivity were nearly within 2 orders of magnitude of the maximum expected value in a range that exceeds 6 orders of magnitude. The estimate of vertical anisotropy was larger than the maximum expected value. All estimates of specific yield and their confidence intervals were within the ranges of values expected for aquifers, the range of values for porosity of basalt, and other estimates of specific yield for basalt. The steady-state model reasonably simulated the observed water-table altitude, orientation, and gradients. Simulation of transient flow conditions accurately reproduced observed changes in the flow system resulting from episodic infiltration from the Big Lost River and facilitated understanding and visualization of the relative importance of historical differences in infiltration in time and space. As described in a conceptual model, the numerical model simulations demonstrate flow that is (1) dominantly horizontal through interflow zones in basalt and vertical anisotropy resulting from contrasts in hydraulic conductivity of various types of basalt and the interbedded sediments, (2) temporally variable due to streamflow infiltration from the Big Lost River, and (3) moving downward downgradient of the INL. The numerical models were reparameterized, recalibrated, and analyzed to evaluate alternative conceptualizations or implementations of the conceptual model. The analysis of the reparameterized models revealed that little improvement in the model could come from alternative descriptions of sediment content, simulated aquifer thickness, streamflow infiltration, and vertical head distribution on the downgradient boundary. Of the alternative estimates of flow to or from the aquifer, only a 20 percent decrease in

Open-File Report↗

USGS2010

Steady-state and transient models of groundwater flow and advective transport, Eastern Snake River Plain aquifer, Idaho National Laboratory and vicinity, Idaho

Scientific Investigations Report↗

USGS2013

The transboundary non-renewable Nubian Aquifer System of Chad, Egypt, Libya and Sudan: Classical groundwater questions and parsimonious hydrogeologic analysis and modeling

Parsimonious groundwater modeling provides insight into hydrogeologic functioning of the Nubian Aquifer System (NAS), the world’s largest non-renewable groundwater system (belonging to Chad, Egypt, Libya, and Sudan). Classical groundwater-resource issues exist (magnitude and lateral extent of drawdown near pumping centers) with joint international management questions regarding transboundary drawdown. Much of NAS is thick, containing a large volume of high-quality groundwater, but receives insignificant recharge, so water-resource availability is time-limited. Informative aquifer data are lacking regarding large-scale response, providing only local-scale information near pumps. Proxy data provide primary underpinning for understanding regional response: Holocene water-table decline from the previous pluvial period, after thousands of years, results in current oasis/sabkha locations where the water table still intersects the ground. Depletion is found to be controlled by two regional parameters, hydraulic diffusivity and vertical anisotropy of permeability. Secondary data that provide insight are drawdowns near pumps and isotope-groundwater ages (million-year-old groundwaters in Egypt). The resultant strong simply structured three-dimensional model representation captures the essence of NAS regional groundwater-flow behavior. Model forecasts inform resource management that transboundary drawdown will likely be minimal—a nonissue—whereas drawdown within pumping centers may become excessive, requiring alternative extraction schemes; correspondingly, significant water-table drawdown may occur in pumping centers co-located with oases, causing oasis loss and environmental impacts.

Hydrogeology Journal↗

USGS2013

Geologic framework, structure, and hydrogeologic characteristics of the Knippa Gap area in eastern Uvalde and western Medina Counties, Texas

The Edwards aquifer is the primary source of potable water for the San Antonio area in south-central Texas. The Knippa Gap was postulated to channel or restrict flow in the Edwards aquifer in eastern Uvalde County, and its existence was based on a series of numerical simulations of groundwater flow in the aquifer. To better understand the function of the area known as the Knippa Gap as it pertains to its geology and structure, the geologic framework, structure, and hydrogeologic characteristics of the area were evaluated by the U.S. Geological Survey in cooperation with the U.S. Army Corps of Engineers-Fort Worth District. The principal structural feature in the San Antonio area is the Balcones Fault Zone, which is the result of Miocene age faulting. In Medina County, the faulting of the Balcones Fault Zone has produced a relay-ramp structure that dips to the southwest from the Edwards aquifer recharge zone and extends westward and below land surface from Seco Creek. Groundwater flow paths in the Edwards aquifer are influenced by faulting and geologic structure. Some faults act as barriers to groundwater flow paths where the aquifer is offset by 50 percent or more and result in flow moving parallel to the fault. The effectiveness of a fault as a barrier to flow changes as the amount of fault displacement changes. The structurally complex area of the Balcones Fault Zone contains relay ramps, which form in extensional fault systems to allow for deformation changes along the fault block. In Medina County, the faulting of the Balcones Fault Zone has produced a relay-ramp structure that dips to the southwest from the Edwards aquifer recharge zone. Groundwater moving down the relay ramp in northern Medina County flows downgradient (downdip) to the structural low (trough) from the northeast to the southwest. In Uvalde County, the beds dip from a structural high known as the Uvalde Salient. This results in groundwater moving from the structural high and downgradient (dip) towards a structural low (trough) to the northeast. These two opposing structural dips result in a subsurface structural low (trough) locally referred to as the Knippa Gap. This trough is located in eastern Uvalde County beneath the towns of Knippa and Sabinal. By using data that were compiled and collected for this study and previous studies, a revised map was constructed depicting the geologic framework, structure, and hydrogeologic characteristics of the Knippa Gap area in eastern Uvalde and western Medina Counties, Tex. The map also shows the interpreted structural dip directions and interpreted location of a structural low (trough) in the area known as the Knippa Gap.

Texas↗

USGS2012

Status of groundwater quality in the Upper Santa Ana Watershed, November 2006--March 2007--California GAMA Priority Basin Project

Groundwater quality in the approximately 1,000-square-mile (2,590-square-kilometer) Upper Santa Ana Watershed (USAW) study unit was investigated as part of the Priority Basin Project of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The study unit is located in southern California in Riverside and San Bernardino Counties. The GAMA Priority Basin Project is being conducted by the California State Water Resources Control Board in collaboration with the U.S. Geological Survey and the Lawrence Livermore National Laboratory. The GAMA USAW study was designed to provide a spatially unbiased assessment of untreated groundwater quality within the primary aquifer systems in the study unit. The primary aquifer systems (hereinafter, primary aquifers) are defined as the perforation interval of wells listed in the California Department of Public Health (CDPH) database for the USAW study unit. The quality of groundwater in shallower or deeper water-bearing zones may differ from that in the primary aquifers; shallower groundwater may be more vulnerable to surficial contamination. The assessment is based on water-quality and ancillary data collected by the U.S. Geological Survey (USGS) from 90 wells during November 2006 through March 2007, and water-quality data from the CDPH database. The status of the current quality of the groundwater resource was assessed based on data from samples analyzed for volatile organic compounds (VOCs), pesticides, and naturally occurring inorganic constituents, such as major ions and trace elements. The status assessment is intended to characterize the quality of groundwater resources within the primary aquifers of the USAW study unit, not the treated drinking water delivered to consumers by water purveyors. Relative-concentrations (sample concentration divided by the health- or aesthetic-based benchmark concentration) were used for evaluating groundwater quality for those constituents that have Federal or California regulatory or non-regulatory benchmarks for drinking-water quality. A relative-concentration greater than (>) 1.0 indicates a concentration above a benchmark, and a relative-concentration less than or equal to (≤) 1.0 indicates a concentration equal to or less than a benchmark. Organic and special-interest constituent relative-concentrations were classified as "high" (> 1.0), "moderate" (0.1 < relative-concentration ≤ 1.0), or "low" (≤ 0.1). Inorganic constituent relative-concentrations were classified as "high" (> 1.0), "moderate" (0.5 < relative-concentration ≤ 1.0), or "low" ( ≤ 0.5). Aquifer-scale proportion was used as the primary metric in the status assessment for evaluating regional-scale groundwater quality. Aquifer-scale proportions are defined as the percentage of the area of the primary aquifer system with concentrations above or below specified thresholds relative to regulatory or aesthetic benchmarks. High aquifer-scale proportion is defined as the percentage of the area of the primary aquifers with a relative-concentration greater than 1.0 for a particular constituent or class of constituents; percentage is based on an areal, rather than a volumetric basis. Moderate and low aquifer-scale proportions were defined as the percentage of the primary aquifers with moderate and low relative-concentrations, respectively. Two statistical approaches—grid-based and spatially weighted—were used to evaluate aquifer-scale proportions for individual constituents and classes of constituents. Grid-based and spatially weighted estimates were comparable in the USAW study unit (within 90-percent confidence intervals). Inorganic constituents with human-health benchmarks had relative-concentrations that were high in 32.9 percent of the primary aquifers, moderate in 29.3 percent, and low in 37.8 percent. The high aquifer-scale proportion of these inorganic constituents primarily reflected high aquifer-scale proportions of nitrate (high relative-concentration in 25.3 percent of the aquifer), although seven other inorganic constituents with human-health benchmarks also were detected at high relative-concentrations in some percentage of the aquifer: arsenic, boron, fluoride, gross alpha activity, molybdenum, uranium, and vanadium. Perchlorate, as a constituent of special interest, was evaluated separately from other inorganic constituents, and had high relative-concentrations in 11.1 percent, moderate in 53.3 percent, and low or not detected in 35.6 percent of the primary aquifers. In contrast to the inorganic constituents, relative-concentrations of organic constituents (one or more) were high in 6.7 percent, moderate in 11.1 percent, and low or not detected in 82.2 percent of the primary aquifers. Of the 237 organic and special-interest constituents analyzed for, 39 constituents were detected (21 VOCs, 13 pesticides, 3 pharmaceuticals, and 2 constituents of special interest). All of the detected VOCs had health-based benchmarks, and five of these—1,1-dichloroethene, 1,2-dibromo-3-chloropropane (DBCP), tetrachloroethene (PCE), carbon tetrachloride, and trichloroethene (TCE)—were detected in at least one sample at a concentration above a benchmark (high relative-concentration). Seven of the 13 pesticides had health-based benchmarks, and none were detected above these benchmarks (no high relative-concentrations). Pharmaceuticals do not have health-based benchmarks. Thirteen organic constituents were frequently detected (detected in at least 10 percent of samples without regard to relative-concentrations): bromodichloromethane, chloroform, cis-1,2-dichloroethene, 1,1-dichloroethene, dichlorodifluoromethane (CFC-12), methyl tert-butyl ether (MTBE), PCE, TCE, trichlorofluoromethane (CFC-11), atrazine, bromacil, diuron, and simazine.

California↗

USGS2006

Contamination of ground water by PCE - A national perspective

Perchloroethylene (PCE) has physical and chemical properties that make it likely to persist in groundwater if released to the environment. The US Geological Survey has collected or compiled data on the occurrence of PCE in groundwater from major aquifers around the US. These data represent the occurrence of PCE in the groundwater resource as a whole and not occurrence at specific release sites. PCE was detected at measurable concentrations in nearly one in 10 wells in major aquifers throughout the country. Trichloroethylene was found most commonly with PCE and its presence may be due, in part, to reductive dechlorination of PCE. This is an abstract of a paper presented at the Petroleum Hydrocarbons and Organic Chemicals in Ground Water: Prevention, Assessment, and Remediation Conference (Houston, TX 11/6-7/2006).

Conference Paper↗

USGS1997

Distribution of terminal electron-accepting processes in an aquifer having multiple contaminant sources

Concentrations of electron acceptors, electron donors, and H2 in groundwater were measured to determine the distribution of terminal electron-accepting processes (TEAPs) in an alluvial aquifer having multiple contaminant sources. Upgradient contaminant sources included two separate hydrocarbon point sources, one of which contained the fuel oxygenate methyl tertbutyl ether (MTBE). Infiltrating river water was a source of dissolved NO31 SO4 and organic carbon (DOC) to the downgradient part of the aquifer. Groundwater downgradient from the MTBE source had larger concentrations of electron acceptors (dissolved O2 and SO4) and smaller concentrations of TEAP end products (dissolved inorganic C, Fe2+ and CH4) than groundwater downgradient from the other hydrocarbon source, suggesting that MTBE was not as suitable for supporting TEAPs as the other hydrocarbons. Measurements of dissolved H2 indicated that SO4 reduction predominated in the aquifer during a period of high water levels in the aquifer and river. The predominant TEAP shifted to Fe3+ reduction in upgradient areas after water levels receded but remained SO4 reducing downgradient near the river. This distribution of TEAPs is the opposite of what is commonly observed in aquifers having a single contaminant point source and probably reflects the input of Dec and SO4 to the aquifer from the river. Results of this study indicate that the distribution of TEAPs in aquifers having multiple contaminant sources depends on the composition and location of the contaminants and on the availability of electron acceptors.

Applied Geochemistry↗

USGS2010

Status and understanding of groundwater quality in the central-eastside San Joaquin Basin, 2006: California GAMA Priority Basin Project

Groundwater quality in the approximately 1,695-square-mile Central Eastside San Joaquin Basin (Central Eastside) study unit was investigated as part of the Priority Basin Project (PBP) of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The GAMA PBP was developed in response to the California Groundwater Quality Monitoring Act of 2001, and is being conducted by the California State Water Resources Control Board in collaboration with the U.S. Geological Survey and the Lawrence Livermore National Laboratory. The GAMA Central Eastside study unit was designed to provide a spatially unbiased assessment of untreated-groundwater quality, as well as a statistically consistent basis for comparing water quality throughout California. During March through June 2006, samples were collected from 78 wells in Stanislaus and Merced Counties, 58 of which were selected using a spatially distributed, randomized grid-based method to provide statistical representation of the study unit (grid wells), and 20 of which were sampled to evaluate changes in water chemistry along groundwater-flow paths (understanding wells). Water-quality data from the California Department of Public Health (CDPH) database also were used for the assessment. An assessment of the current status of the groundwater quality included collecting samples from wells for analysis of anthropogenic constituents such as volatile organic compounds (VOCs) and pesticides, as well as naturally occurring constituents such as major ions and trace elements. The assessment of status is intended to characterize the quality of untreated-groundwater resources within the primary aquifer system, not the treated drinking water delivered to consumers by water purveyors. The primary aquifer system (hereinafter, primary aquifer) is defined as that part of the aquifer corresponding to the perforation interval of wells listed in the CDPH database for the Central Eastside study unit. The quality of groundwater in shallower or deeper water-bearing zones may differ from that in the primary aquifer; shallower groundwater may be more vulnerable to surficial contamination. The primary aquifer is represented by the grid wells, of which 90 percent had depths to the tops of their perforations of about 80 to 330 feet and depths to bottom of about 100 to 670 feet. Relative-concentrations (sample concentration divided by benchmark concentration) were used as the primary metric for assessing the status of water quality for those constituents that have Federal and (or) California human health or aesthetic benchmarks. A relative-concentration greater than (>) 1.0 indicates a concentration above a benchmark, and less than or equal to (≤) 1.0 indicates a concentration equal to or below a benchmark. For organic and special interest constituents, relative-concentrations were classified as high (>1.0), moderate (≤1.0 and >0.1), or low (≤0.1). For inorganic constituents, relative-concentrations were classified as high (>1.0), moderate (≤1.0 and >0.5), or low (≤0.5). The threshold between low and moderate classifications was lower for organic and special interest constituents than for inorganic constituents because organic constituents generally are less prevalent and have smaller relative-concentrations than inorganic constituents. Grid-based and spatially-weighted approaches, the latter incorporating data from all CDPH wells, were used to evaluate the proportion of the primary aquifer (aquifer-scale proportions) with high, moderate, or low relative-concentrations. For individual constituents or classes of constituents, the aquifer-scale high proportion is the percentage of the area of the study unit having high relative-concentrations within the depth-zones of the primary aquifer. Aquifer-scale moderate and low proportions are defined similarly. Spatially-weighted aquifer-scale high proportions nearly always fell within the 90-percent confidence interval of grid-based aquifer-scale high proportions, indicating that the grid-based approach yielded statistically equivalent results to the spatially-weighted approach incorporating CDPH data. The status assessment for inorganic constituents showed that inorganic constituents (one or more) were high, relative to human-health benchmarks, in 18.0 percent of the primary aquifer, moderate in 44.0 percent, and low in 38.0 percent. Of inorganic constituents with human-health benchmarks, arsenic, vanadium, and nitrate were detected at high relative-concentrations in 15.6 percent, 3.6 percent, and 2.1 percent, respectively, of the primary aquifer. Of inorganic constituents with secondary maximum contaminant levels (SMCL), manganese, iron, and TDS were detected at high relative-concentrations in 4.5 percent, 2.2 percent, and 1.7 percent, respectively, of the primary aquifer. The status assessment for organic constituents showed that organic constituents (one or more) were high, relative to human-health benchmarks, in a smaller proportion of the primary aquifer (1.2 percent) than inorganic constituents (18.0 percent). Organic constituents had moderate relative-concentrations in 14.3 percent, and had low relative-concentrations or were not detected in 84.5 percent, of the primary aquifer. The proportion of the primary aquifer with high relative-concentrations of organic constituents reflected high proportions of the discontinued soil fumigant 1,2-dibromo-3-chlororopane (DBCP; 1.0 percent) and the solvent tetrachloroethene (PCE; 0.2 percent). Most of the organic and special interest constituents detected in groundwater in the Central Eastside study unit have human-health benchmarks. Of the 205 organic and special interest constituents analyzed for, 36 constituents were detected. Of these constituents, 32 were detected only at low relative-concentrations. Four constituents, chloroform, carbon tetrachloride, DBCP, and perchlorate, were detected at moderate relative-concentrations in grid wells. Nine organic and special-interest constituents were detected frequently (detected in greater than 10 percent of samples): the trihalomethanes chloroform, bromoform, bromodichloromethane, and dibromochloromethane; the solvent PCE; the herbicides atrazine, simazine, and metolachlor, and special-interest constituent perchlorate. An assessment of understanding of the groundwater quality included sampling of understanding wells, some of which were perforated in shallower or deeper portions of the aquifer system than the primary aquifer, and analysis of correlations of groundwater quality with land use, depth, age classification, and other potential explanatory factors. The understanding assessment indicated that the concentrations of many constituents were related to depth and groundwater age. However, concentrations of individual constituents or constituent classes also were sometimes related to geochemical conditions, lateral position in the flow system, or land use. High and moderate relative-concentrations of uranium, nitrate, and total dissolved solids (TDS) were detected in some wells where the tops of perforations are within the upper 200 feet of the aquifer system. In wells with the depth to the top of perforations below this depth, concentrations were low. A similar pattern occurred for the sum of herbicide concentrations. These vertical water-chemistry patterns are consistent with the hydrogeologic setting, in which return flows from agricultural and urban land use are the major source of recharge, and withdrawals for irrigation and urban supply are the major source of discharge, resulting in substantial vertical components of groundwater flow. The decrease in concentrations of many constituents with depth reflects in part that groundwater gets older with depth. Tritium, helium-isotopes, and carbon-14 data were used to classify the predominant age of groundwater samples into three categories: modern (water that has entered the aquifer in the last 50 years), pre-modern (water that entered the aquifer more than 50 years, up to tens of thousands of years, ago), and mixed (mixtures of waters with modern and pre-modern ages). Uranium, nitrate, and herbicide concentrations were significantly higher in groundwater having modern- and mixed-ages than pre-modern ages, indicating that these constituents may be affected by anthropogenic activities in the last 50 years. Other patterns in the distribution of nitrate, uranium, and TDS are evident. Isotopic and geochemical data are consistent with partial denitrification of nitrate in some reducing groundwaters in the western and deeper parts of the flow system. Uranium and TDS concentrations increase from east to west across the valley, along the direction of regional lateral groundwater flow. High and moderate relative-concentrations of arsenic can be attributed to reductive dissolution of manganese or iron oxides, or to desorption by high pH waters. Arsenic concentrations also increased with increasing depth and groundwater age. High to moderate relative-concentrations of vanadium primarily are related to high pH under oxic conditions. The frequency of detections of DBCP was greater in areas with orchard-vineyard land use >40 percent and at depths <200 feet. THMs and solvents were correlated positively with percent urban land use. Herbicide concentrations were correlated negatively with percent natural land use. Perchlorate concentrations were significantly greater in waters having modern and mixed ages than waters having pre-modern ages and were significantly and positively correlated with two land uses—percent orchard/vineyard land use and percent urban land use.

California↗

USGS2015

Potentiometric surfaces and water-level trends in the Cockfield (upper Claiborne) aquifer in southern Arkansas and the Wilcox (lower Wilcox) aquifer of northeastern and southern Arkansas, 2012

The Cockfield aquifer, located in southern Arkansas, is composed of Eocene-age sand beds found near the base of the Cockfield Formation of Claiborne Group. The Wilcox aquifer, located in northeastern and southern Arkansas, is composed of Paleocene-age sand beds found in the middle to lower part of the Wilcox Group. The Cockfield and Wilcox aquifers are primary sources of groundwater. In 2010, withdrawals from the Cockfield aquifer in Arkansas totaled 19.2 million gallons per day (Mgal/d), and withdrawals from the Wilcox aquifer totaled 36.5 Mgal/d. A study was conducted by the U.S. Geological Survey in cooperation with the Arkansas Natural Resources Commission and the Arkansas Geological Survey to measure water levels associated with the Cockfield aquifer and the Wilcox aquifer in northeastern and southern Arkansas. Water levels were measured at 43 wells completed in the Cockfield aquifer and 47 wells completed in the Wilcox aquifer in February and March 2012. Measurements from 2012 are presented as potentiometric-surface maps and in combination with measurements from 2006 as water-level difference maps. Trends in water-level change over time within the Cockfield and Wilcox aquifers were determined using the water-level difference maps and selected well hydrographs. The Cockfield aquifer study area in southern Arkansas is bounded on the east by the Mississippi River and on the west by the area that contains outcrops and subcrops of the Cockfield Formation. The northern boundary of the Cockfield aquifer study area is defined by the area that contains observation wells completed in the Cockfield aquifer and the southern boundary is the Louisiana State line. The Wilcox aquifer study area in northeastern Arkansas is bounded on the east by the Mississippi River and on the north by the Missouri State line. The southern and western boundaries are defined by areas containing observation wells completed in the Wilcox aquifer or by outcrop areas on or near Crowleys Ridge. The Wilcox aquifer study area in southern Arkansas is defined by observation wells completed in the Wilcox aquifer or by areas that contain outcrops of the Wilcox Group, or both. The potentiometric-surface map of the Cockfield aquifer shows the regional direction of groundwater flow was generally toward the east-southeast, except in areas of intense groundwater withdrawals such as southwestern Ashley County, where groundwater flows toward the town of Crossett. The highest water-level altitude measured was 350 feet (ft) above National Geodetic Vertical Datum of 1929 (NGVD 29) in central Columbia County. The lowest water-level altitude measured was 40 ft above NGVD 29 in southeastern Lincoln County. The water-level difference map for the Cockfield aquifer in Arkansas was constructed using 42 water-level measurements made during 2006 and 2012. The difference in water levels for the Cockfield aquifer ranged from 27.4 ft to -10.4 ft. The largest water-level rise was in Calhoun County, and the largest water-level decline was 10.4 ft in Union County. Of the 42 wells, 13 wells had a rise in water level, and the remaining 29 wells had a decline in water level. Hydrographs for 32 wells in the Cockfield aquifer with historical water-level data were evaluated using linear regression to calculate the annual rise or decline for each well. These data were aggregated by county and statistically evaluated for the range, mean, and median of water-level change in each county. Hydrographs for Bradley, Calhoun, Chicot, Columbia, and Union Counties indicated both rising and declining water levels. The mean annual water-level rise or decline for Calhoun County was 0.00 foot per year (ft/yr) or unchanged. The mean annual water-level for Ashley, Bradley, Chicot, Cleveland, Columbia, Lincoln, and Union Counties show declines ranging from -0.02 to -1.10 ft/yr. Two potentiometric-surface maps, one for the southern area and one for the northeastern area, were constructed to show the altitude of the water surface in the Wilcox aquifer. The direction of groundwater flow in the northeastern area was generally towards the south-southwest except for some areas immediately adjacent to the Mississippi River where the flow was more eastward towards the river. The highest water-level altitude was 219 ft in northern Mississippi County, and the lowest water-level altitude was 123 ft near West Memphis in Crittenden County. The direction of groundwater flow in the northern part of the southern area was generally towards the southwest. The direction of groundwater flow in the southern part was in all directions because of two cones of depression and two water-level mounds. The highest water-level altitude measured was 394 ft at the center of a water-level mound in eastern Hot Spring County and a water-level mound in southwestern Hempstead County. The lowest water-level altitude measured was 145 ft at the center of the cone of depression in Clark County. Water-level difference maps for the Wilcox aquifer in Arkansas were constructed using 47 water-level measurements made during 2006 and 2012. The difference in water levels for the Wilcox aquifer in the northeastern area ranged from 22.0 ft to -17.9 ft. The largest rise in water level occurred in Crittenden County, and the largest decline occurred in Lee County. Twenty-one wells had rising water levels, and 10 wells had declining water levels. The difference in water levels for the Wilcox aquifer in the southern area ranged from 18.1 ft to -4.2 ft. The largest rise and the largest decline in water level occurred in Nevada County. Twelve wells had rising water levels, and 4 wells had declining water levels. Linear regression analysis of long-term hydrographs was used to determine the mean annual water-level rise and decline in the Wilcox aquifer in the northeastern and southern areas of Arkansas. In the northeastern area, the mean annual water level declined in all seven counties. The mean annual declines ranged from -0.55 ft/yr in Craighead County to -1.46 ft/yr in St. Francis County. In the southern area, the annual rise and decline calculations for wells with over 20 years of records indicate rising and declining water levels in Clark, Hot Spring, and Nevada Counties. The mean annual water level declined in all counties except Hot Spring County.

Arkansas↗

USGS2024

Hydroacoustic observations reveal drivers of mixing and salinization of a karst subterranean estuary during intense precipitation

Karst subterranean estuaries within globally ubiquitous carbonate aquifers are coastal groundwater ecosystems that provide an essential water resource for human populations. To understand the drivers of salinization within a coastal aquifer in the Yucatan Peninsula (Mexico), we employed hydroacoustics in flooded caves to observe how oceanic and atmospheric events facilitate mixing between the meteoric lens (fresh-brackish groundwater) and the saline groundwater on tidal and episodic timescales. Precipitation during Tropical Storm Carlotta increased the flow and salinity of the meteoric lens without evidence for vertical mixing across the halocline. We postulate that vertical migration of haloclines in the conduit relative to those within the rock matrix during precipitation creates lateral density gradients that drive mixing, and ultimately creates a brackish layer within the meteoric lens. These results provide a mechanistic explanation for vertical and lateral exchange in a coastal carbonate aquifer, which has implications for groundwater response to future climatic change.

Ox Bel Ha cave system, Yucatan peninsula↗

USGS2010

Effects of groundwater-flow paths on nitrate concentrations across two riparian forest corridors

Groundwater levels, apparent age, and chemistry from field sites and groundwater-flow modeling of hypothetical aquifers collectively indicate that groundwater-flow paths contribute to differences in nitrate concentrations across riparian corridors. At sites in Virginia (one coastal and one Piedmont), lowland forested wetlands separate upland fields from nearby surface waters (an estuary and a stream). At the coastal site, nitrate concentrations near the water table decreased from more than 10 mg/L beneath fields to 2 mg/L beneath a riparian forest buffer because recharge through the buffer forced water with concentrations greater than 5 mg/L to flow deeper beneath the buffer. Diurnal changes in groundwater levels up to 0.25 meters at the coastal site reflect flow from the water table into unsaturated soil where roots remove water and nitrate dissolved in it. Decreases in aquifer thickness caused by declines in the water table and decreases in horizontal hydraulic gradients from the uplands to the wetlands indicate that more than 95% of the groundwater discharged to the wetlands. Such discharge through organic soil can reduce nitrate concentrations by denitrification. Model simulations are consistent with field results, showing downward flow approaching toe slopes and surface waters to which groundwater discharges. These effects show the importance of buffer placement over use of fixed-width, streamside buffers to control nitrate concentrations.

Virginia↗

USGS2011

Modeling the potential impact of seasonal and inactive multi-aquifer wells on contaminant movement to public water-supply wells

Wells screened across multiple aquifers can provide pathways for the movement of surprisingly large volumes of groundwater to confined aquifers used for public water supply (PWS). Using a simple numerical model, we examine the impact of several pumping scenarios on leakage from an unconfined aquifer to a confined aquifer and conclude that a single inactive multi-aquifer well can contribute nearly 10% of total PWS well flow over a wide range of pumping rates. This leakage can occur even when the multi-aquifer well is more than a kilometer from the PWS well. The contribution from multi-aquifer wells may be greater under conditions where seasonal pumping (e.g., irrigation) creates large, widespread downward hydraulic gradients between aquifers. Under those conditions, water can continue to leak down a multi-aquifer well from an unconfined aquifer to a confined aquifer even when those multi-aquifer wells are actively pumped. An important implication is that, if an unconfined aquifer is contaminated, multi-aquifer wells can increase the vulnerability of a confined-aquifer PWS well.

Journal of the American Water Resources Associatio↗

USGS2010

Groundwater quality of the Gulf Coast aquifer system, Houston, Texas, 2007-08

In the summers of 2007 and 2008, the U.S. Geological Survey (USGS), in cooperation with the City of Houston, Texas, completed an initial reconnaissance-level survey of naturally occurring contaminants (arsenic, other selected trace elements, and radionuclides) in water from municipal supply wells in the Houston area. The purpose of this reconnaissance-level survey was to characterize source-water quality prior to drinking water treatment. Water-quality samples were collected from 28 municipal supply wells in the Houston area completed in the Evangeline aquifer, Chicot aquifer, or both. This initial survey is part of ongoing research to determine concentrations, spatial extent, and associated geochemical conditions that might be conducive for mobility and transport of these constituents in the Gulf Coast aquifer system in the Houston area. Samples were analyzed for major ions (calcium, magnesium, potassium, sodium, bromide, chloride, fluoride, silica, and sulfate), selected chemically related properties (residue on evaporation [dissolved solids] and chemical oxygen demand), dissolved organic carbon, arsenic species (arsenate [As(V)], arsenite [As(III)], dimethylarsinate [DMA], and monomethylarsonate [MMA]), other trace elements (aluminum, antimony, arsenic, barium, beryllium, boron, cadmium, chromium, cobalt, copper, iron, lead, lithium, manganese, molybdenum, nickel, selenium, silver, strontium, thallium, vanadium, and zinc), and selected radionuclides (gross alpha- and beta-particle activity [at 72 hours and 30 days], carbon-14, radium isotopes [radium-226 and radium-228], radon-222, tritium, and uranium). Field measurements were made of selected physicochemical (relating to both physical and chemical) properties (oxidation-reduction potential, turbidity, dissolved oxygen concentration, pH, specific conductance, water temperature, and alkalinity) and unfiltered sulfides. Dissolved organic carbon and chemical oxygen demand are presented but not discussed in the report. Physicochemical properties, major ions, and trace elements varied considerably. The pH ranged from 7.2 to 8.1 (median 7.6); specific conductance ranged from 314 to 856 microsiemens per centimeter at 25 degrees Celsius, with a median of 517 microsiemens per centimeter; and alkalinity ranged from 126 to 324 milligrams per liter as calcium carbonate (median 167 milligrams per liter). The range in oxidation-reduction potential was large, from -212 to 244 millivolts, with a median of -84.6 millivolts. The largest ranges in concentration for filtered major ion constituents were obtained for cations sodium and calcium and for anions chloride and bicarbonate (bicarbonate was calculated from the measured alkalinity). Filtered arsenic was detected in all 28 samples, ranging from 0.58 to 15.3 micrograms per liter (median 2.5 micrograms per liter), and exceeded the maximum contaminant level established by the U.S. Environmental Protection Agency of 10 micrograms per liter in 2 of the 28 samples. As(III) was the most frequently detected arsenic specie. As(III) concentrations ranged from less than 0.6 to 14.9 micrograms arsenic per liter. The range in concentrations for the arsenic species As(V) was from less than 0.8 to 3.3 micrograms arsenic per liter. Barium, boron, lithium, and strontium were detected in quantifiable (equal to or greater than the laboratory reporting level) concentrations in all samples and molybdenum in all but one sample. Filtered iron, manganese, nickel, and vanadium were each detected in at least 18 of the 28 samples. All other selected trace elements were each detected in 16 or fewer samples. Radionuclides were detected in most samples. The gross alpha-particle activities at 30 days and 72 hours ranged from R-0.94 to 15.5 and R-1.1 to 17.2 picocuries per liter, respectively ('R' indicates nondetected result less than the sample-specific critical level). The combined radium (radium-226 plus radium-228) concentrations ranged from an estimat

Texas↗

USGS2024

Comparison of water quality in shallow groundwater near agricultural areas in the Delaware Coastal Plain, 2014 and 2019

The State of Delaware has encouraged agricultural conservation practices to improve nutrient uptake by crops and mitigate nutrient transport to groundwater in the surficial aquifer. To study recent changes in groundwater quality, the U.S. Geological Survey and the Delaware Department of Agriculture (DDA) developed a network of shallow wells near agricultural areas throughout the Delaware Coastal Plain. This network was designed to characterize water quality related to agricultural practices and to detect any recent changes in shallow groundwater quality, in particular groundwater nitrate concentrations. The shallow well network was first sampled in 2014 and resampled in 2019. In 2019, field parameters (including dissolved oxygen, pH, specific conductance, and temperature), major ions, nutrients, stable isotopes of water, and isotopes of nitrate were measured in groundwater samples collected between October and December. Wells were organized into three groups based on their geochemical characteristics measured in 2014: the Agricultural, Urban, and Mixed Groups. Results from the 2019 sampling showed little change in water quality from the 2014 sampling. Land-use factors continued to be the driving influence between groups. Groundwater moves slowly and changes in groundwater quality are likely to respond slowly to changes in conservation practices. Continued sampling of both groundwater quality in this network and monitoring land management practices can help detect groundwater quality trends in the future.

Delaware↗

USGS2004

Using geochemical data and aquifer simulation to characterize recharge and groundwater flow in the Middle Rio Grande Basin, New Mexico

No abstract available.

New Mexico↗

USGS2011

Status and understanding of groundwater quality in the Monterey Bay and Salinas Valley Basins, 2005-California GAMA Priority Basin Project

Groundwater quality in the approximately 1,000 square mile (2,590 km2) Monterey Bay and Salinas Valley Basins (MS) study unit was investigated as part of the Priority Basin Project of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The study unit is located in central California in Monterey, Santa Cruz, and San Luis Obispo Counties. The GAMA Priority Basin Project is being conducted by the California State Water Resources Control Board in collaboration with the U.S. Geological Survey (USGS) and the Lawrence Livermore National Laboratory. The GAMA MS study was designed to provide a spatially unbiased assessment of the quality of untreated (raw) groundwater in the primary aquifer systems (hereinafter referred to as primary aquifers). The assessment is based on water-quality and ancillary data collected in 2005 by the USGS from 97 wells and on water-quality data from the California Department of Public Health (CDPH) database. The primary aquifers were defined by the depth intervals of the wells listed in the CDPH database for the MS study unit. The quality of groundwater in the primary aquifers may be different from that in the shallower or deeper water-bearing zones; shallow groundwater may be more vulnerable to surficial contamination. The first component of this study, the status of the current quality of the groundwater resource, was assessed by using data from samples analyzed for volatile organic compounds (VOC), pesticides, and naturally occurring inorganic constituents, such as major ions and trace elements. This status assessment is intended to characterize the quality of groundwater resources in the primary aquifers of the MS study unit, not the treated drinking water delivered to consumers by water purveyors. Relative-concentrations (sample concentration divided by the health- or aesthetic-based benchmark concentration) were used for evaluating groundwater quality for those constituents that have Federal and (or) California regulatory or non-regulatory benchmarks for drinking-water quality. A relative-concentration greater than (>) 1.0 indicates a concentration greater than a benchmark, and less than or equal to (≤) 1.0 indicates a concentration less than or equal to a benchmark. Relative-concentrations of organic and special interest constituents [perchlorate, N-nitrosodimethylamine (NDMA), and 1,2,3-trichloropropane (1,2,3-TCP)], were classified as "high" (relative-concentration > 1.0), "moderate" (0.1 < relative-concentration ≤ 1.0), or "low" (relative-concentration ≤ 0.1). Relative-concentrations of inorganic constituents were classified as "high" (relative-concentration > 1.0), "moderate" (0.5 < relative-concentration ≤ 1.0), or "low" (relative-concentration ≤ 0.5). Aquifer-scale proportion was used as the primary metric in the status assessment for evaluating regional-scale groundwater quality. High aquifer-scale proportion was defined as the percentage of the area of the primary aquifers with a relative-concentration greater than 1.0 for a particular constituent or class of constituents; percentage is based on an areal rather than a volumetric basis. Moderate and low aquifer-scale proportions were defined as the percentage of the primary aquifers with moderate and low relative-concentrations, respectively. Two statistical approaches-grid-based and spatially weighted-were used to evaluate aquifer-scale proportions for individual constituents and classes of constituents. Grid-based and spatially-weighted estimates were comparable in the MS study unit (within 90-percent confidence intervals). Inorganic constituents with human-health benchmarks were detected at high relative-concentrations in 14.5 percent of the primary aquifers, moderate in 35.5 percent, and low in 50.0 percent. High aquifer-scale proportion of inorganic constituents primarily reflected high aquifer-scale proportions of nitrate (7.9 percent), molybdenum (2.9 percent), arsenic (2.8 percent), boron (1.9 percent), and gross alpha-beta radioactivity (1.5 percent). Relative-concentrations of organic constituents (one or more) were high in 0.2 percent, moderate in 6.6 percent, and low in 93.2 percent (not detected in 48.1 percent) of the primary aquifers. The high aquifer-scale proportion of organic constituents primarily reflected high aquifer-scale proportions of tetrachloroethene (0.1 percent) and methyl tert-butyl ether (0.1 percent). Relative-concentration for inorganic constituents with secondary maximum contaminant levels, manganese, total dissolved solids, iron, sulfate, and chloride were high in 18.6, 8.6, 7.1, 2.9, and 1.4 percent of the primary aquifers, respectively. Of the 205 organic and special-interest constituents analyzed, 32 constituents were detected. One organic constituent, the herbicide simazine, was frequently detected (in 10 percent or more of samples), but was detected at low relative-concentrations. The second component of this study, the understanding assessment, identified the natural and human factors that affect groundwater quality by evaluating land use, physical characteristics of the wells, and geochemical conditions of the aquifer. Results from these evaluations were used to explain the occurrence and distribution of constituents in the study unit. The understanding assessment indicated that most wells that contained nitrate were classified as being in agricultural land-use areas, and depths to the top of perforations in most of the wells were less than 350 ft (76 m). High and moderate relative-concentrations of arsenic may be attributed to reductive dissolution of manganese or iron oxides, or to desorption or inhibition of arsenic sorption under alkaline conditions. Arsenic concentrations increased with increasing groundwater depth and residence time (age). Simazine was detected more often in groundwater from wells with surrounding land use classified as agricultural or urban, and with top of perforation depths less than 200 ft (61 m), than in groundwater from wells with natural land use or with deeper depths. Tritium, helium-isotope, and carbon-14 data were used to classify the predominant age of groundwater samples into three categories: modern (water that has entered the aquifer since 1953), pre-modern (water that entered the aquifer prior to 1953 to tens of thousands of years ago), and mixed (mixtures of modern- and pre-modern-age waters). Arsenic concentrations were significantly greater in groundwater with pre-modern age classification than in groundwater with modern-age classification, suggesting that arsenic accumulates with groundwater residence time.

Scientific Investigations Report↗

USGS2011

Status and understanding of groundwater quality in the Santa Clara River Valley, 2007-California GAMA Priority Basin Project

Groundwater quality in the approximately 460-square-mile Santa Clara River Valley study unit was investigated from April through June 2007 as part of the Priority Basin Project of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The GAMA Priority Basin Project is conducted by the U.S. Geological Survey (USGS) in collaboration with the California State Water Resources Control Board and the Lawrence Livermore National Laboratory. The Santa Clara River Valley study unit contains eight groundwater basins located in Ventura and Los Angeles Counties and is within the Transverse and Selected Peninsular Ranges hydrogeologic province. The Santa Clara River Valley study unit was designed to provide a spatially unbiased assessment of the quality of untreated (raw) groundwater in the primary aquifer system. The assessment is based on water-quality and ancillary data collected in 2007 by the USGS from 42 wells on a spatially distributed grid, and on water-quality data from the California Department of Public Health (CDPH) database. The primary aquifer system was defined as that part of the aquifer system corresponding to the perforation intervals of wells listed in the CDPH database for the Santa Clara River Valley study unit. The quality of groundwater in the primary aquifer system may differ from that in shallow or deep water-bearing zones; for example, shallow groundwater may be more vulnerable to surficial contamination. Eleven additional wells were sampled by the USGS to improve understanding of factors affecting water quality.The status assessment of the quality of the groundwater used data from samples analyzed for anthropogenic constituents, such as volatile organic compounds (VOCs) and pesticides, as well as naturally occurring inorganic constituents, such as major ions and trace elements. The status assessment is intended to characterize the quality of untreated groundwater resources in the primary aquifers of the Santa Clara River Valley study unit, not the quality of treated drinking water delivered to consumers. Relative-concentrations (sample concentration divided by health- or aesthetic-based benchmark concentration) were used for evaluating groundwater quality for those constituents that have Federal and (or) California benchmarks. A relative-concentration greater than 1.0 indicates a concentration greater than a benchmark. For organic and special interest constituents, relative-concentrations were classified as high (greater than 1.0); moderate (greater than 0.1 and less than or equal to 1.0); and low (less than or equal to 0.1). For inorganic constituents, relative-concentrations were classified as high (greater than 1.0); moderate (greater than 0.5 and less than or equal to 1.0); and low (less than or equal to 0.5). Aquifer-scale proportion was used as the primary metric in the status assessment for evaluating regional-scale groundwater quality. High aquifer-scale proportion is defined as the areal percentage of the primary aquifer system with relative-concentrations greater than 1.0. Moderate and low aquifer-scale proportions are defined as the areal percentage of the primary aquifer system with moderate and low relative-concentrations, respectively. Two statistical approaches, grid-based and spatially weighted, were used to evaluate aquifer-scale proportions for individual constituents and classes of constituents. Grid-based and spatially weighted estimates were comparable in the Santa Clara River Valley study unit (within 90 percent confidence intervals). The status assessment showed that inorganic constituents were more prevalent and relative-concentrations were higher than for organic constituents. For inorganic constituents with human-health benchmarks, relative-concentrations (of one or more constituents) were high in 21 percent of the primary aquifer system areally, moderate in 30 percent, and low or not detected in 49 percent. Inorganic constituents with human-health benchmarks with high aquifer-scale proportions were nitrate (15 percent of the primary aquifer system), gross alpha radioactivity (14 percent), vanadium (3.4 percent), boron (3.2 percent), and arsenic (2.3 percent). For inorganic constituents with aesthetic benchmarks, relative-concentrations (of one or more constituents) were high in 54 percent of the primary aquifer system, moderate in 41 percent, and low or not detected in 4 percent. The inorganic constituents with aesthetic benchmarks with high aquifer-scale proportions were total dissolved solids (35 percent), sulfate (22 percent), manganese (38 percent), and iron (22 percent). In contrast, the results of the status assessment for organic constituents with human-health benchmarks showed that relative-concentrations were high in 0 percent (not detected above benchmarks) of the primary aquifer system, moderate in 2.4 percent, and low or not detected in 97 percent. Relative-concentrations of the special interest constituent, perchlorate, were moderate in 12 percent of the primary aquifer system and low or not detected in 88 percent. Relative-concentrations of two VOCs-carbon tetrachloride and trichloroethene (TCE)-were moderate in 2.4 percent of the primary aquifer system. One VOC-chloroform (water disinfection byproduct)-was detected in more than 10 percent of the primary aquifer system but at low relative-concentrations. Of the 88 VOCs and gasoline oxygenates analyzed, 71 were not detected. Pesticides were low or not detected in 100 percent of the primary aquifer system. Of the 118 pesticides and pesticide degradates analyzed, 13 were detected and 5 of those had human-health benchmarks. Two of these five pesticides-simazine and atrazine-were detected in more than 10 percent of the primary aquifer system. The second component of this study, the understanding assessment, was to identify the natural and human factors that affect groundwater quality on the basis of the evaluation of land use, physical characteristics of the wells, and geochemical conditions of the aquifer. Results from these analyses are used to explain the occurrence and distribution of selected constituents in the primary aquifer system of the Santa Clara River Valley study unit. The understanding assessment indicated that water quality varied spatially primarily in relation to depth, groundwater age, reduction-oxidation conditions, pH, and location in the regional groundwater flow system. High and moderate relative-concentrations of nitrate and low relative-concentrations of pesticides were correlated with shallow depths to top-of-perforation, and with high dissolved oxygen. Groundwater of modern and mixed ages had higher nitrate than pre-modern-age groundwater. Decreases in concentrations of total dissolved solids (TDS) and sulfate were correlated with increases in pH. This relationship probably indicates relations of these constituents with increasing depth across most of the Santa Clara River Valley study unit. Previous studies have indicated multiple sources of high concentrations of TDS and sulfate and multiple geochemical processes affecting these constituents in the Santa Clara River Valley study unit. Manganese and iron concentrations were highest in pre-modern-age groundwater at depth and in the downgradient area of the Santa Clara River Valley study unit (closest to the coastline), indicating the prevalence of reducing groundwater conditions in these aquifer zones.

Scientific Investigations Report↗

USGS2023

Potentiometric surfaces (2013, 2015), groundwater quality (2010–15), and water-level changes (2011–13, 2013–15) in the Sparta-Memphis aquifer in Arkansas

The Sparta-Memphis aquifer, present across much of eastern Arkansas, is the second most used groundwater resource in the State, with the Mississippi River Valley alluvial aquifer being the primary groundwater resource. The U.S. Geological Survey, in cooperation with Arkansas Department of Agriculture-Natural Resources Division, Arkansas Geological Survey, Natural Resources Conservation Service, Union County Water Conservation Board, and the Union County Conservation District, collects groundwater data across the Sparta-Memphis aquifer extent in Arkansas. This report presents water-level data for measurements conducted during two time periods, January–May 2013 and January–June 2015, and discusses water-level altitude changes for the 2011–13 and 2013–15 periods in the Sparta-Memphis aquifer. Accompanying water-level data in this report include groundwater-quality data for the period 2010–15 in the Sparta-Memphis aquifer. Groundwater data can guide ongoing and future groundwater-monitoring efforts and inform management of the aquifers in Arkansas. Water levels measured at 306 wells from January to May 2013 and 273 wells from January to June 2015 are graphically presented as potentiometric-surface maps. Measurements from 2011, 2013, and 2015 were used in the construction of 2011–13 and 2013–15 water-level change maps. Select long-term hydrographs are included in the report to illustrate water-level changes at the local scale. Water-level data show the influence of climate, pumping, and conservation and management efforts on groundwater levels. With respect to climate, the study area experienced extreme drought conditions between January 2011 and December 2012. The proximate effects of drought—increased evapotranspiration, decreased recharge, and increased irrigation needs—resulted in water-level declines that were particularly notable in the northern and central portions of the study area. Groundwater sampled in 2010–15 from 148 wells completed in the Sparta-Memphis aquifer was analyzed for specific conductance, pH, chloride (Cl) concentration, and bromide (Br) concentration. In 2015, groundwater-quality data from 103 wells completed in the Sparta-Memphis aquifer had a median specific conductance of 356 microsiemens per centimeter at 25 degrees Celsius and a median Cl concentration of 9.5 milligrams per liter (mg/L). The data show two areas of higher Cl (greater than 10 mg/L) and higher Br (greater than 0.5 mg/L) concentrations in Union, Calhoun, and Bradley Counties in southern Arkansas and Monroe and Phillips Counties in eastern-central Arkansas. A Cl and Br mixing model indicates the two regions of wells may have different sources of higher salinity. In the greater Union County area, water in most wells may be a mixture of recharge or precipitation and higher salinity groundwater from the Nacatoch aquifer. Water in wells in eastern-central Arkansas may be sourced from aquifers having a higher Cl concentration (and thus, also a higher Cl-to-Br ratio).

Arkansas↗