Geology topics

Groundwater & aquifers

Find USGS groundwater and aquifer publications. Search an aquifer name or place, compare source-supplied dates and open reports for hydrogeology, recharge and water-level studies.

Follow this topic with RSS

At least 829 records · Page 46Linked to original sources

USGS2004

Mineral dissolution in the Cape Cod aquifer, Massachusetts, USA: I . Reaction stoichiometry and impact of accessory feldspar and glauconite on strontium isotopes, solute concentrations, and REY distribution

To compare relative reaction rates of mineral dissolution in a mineralogically simple groundwater aquifer, we studied the controls on solute concentrations, Sr isotopes, and rare earth element and yttrium (REY) systematics in the Cape Cod aquifer. This aquifer comprises mostly carbonate-free Pleistocene sediments that are about 90% quartz with minor K-feldspar, plagioclase, glauconite, and Fe-oxides. Silica concentrations and pH in the groundwater increase systematically with increasing depth, while Sr isotopic ratios decrease. No clear relationship between 87 Sr/ 86 Sr and Sr concentration is observed. At all depths, the 87 Sr/ 86 Sr ratio of the groundwater is considerably lower than the Sr isotopic ratio of the bulk sediment or its K-feldspar component, but similar to that of a plagioclase-rich accessory separate obtained from the sediment. The Si- 87 Sr/ 86 Sr-depth relationships are consistent with dissolution of accessory plagioclase. In addition, solutes such as Sr, Ca, and particularly K show concentration spikes superimposed on their respective general trends. The K-Sr- 87 Sr/ 86 Sr systematics suggests that accessory glauconite is another major solute source to Cape Cod groundwater. Although the authigenic glauconite in the Cape Cod sediment is rich in Rb, it is low in in-grown radiogenic 87 Sr because of its young Pleistocene age. The low 87 Sr/ 86 Sr ratios are consistent with equilibration of glauconite with seawater. The impact of glauconite is inferred to vary due to its variable abundance in the sediments. In the Cape Cod groundwater, the variation of REY concentrations with sampling depth resembles that of K and Rb, but differs from that of Ca and Sr. Shale-normalized REY patterns are light REY depleted, show negative Ce anomalies and super-chondritic Y/Ho ratios, but no Eu anomalies. REY input from feldspar, therefore, is insignificant compared to input from a K-Rb-bearing phase, inferred to be glauconite. These results emphasize that interpretation of groundwater chemistry, even in relatively simple aquifers, may be complicated by solute contributions from “exotic” accessory minerals such as glauconite. To detect such peculiarities, groundwater studies should combine the study of elemental concentration and isotopic composition of several solutes that show different geochemical behavior.

Massachusetts↗

USGS2021

Complexity of groundwater age mixing near a seawater intrusion zone based on multiple tracers and Bayesian inference

Aquifer flow systems near seawater interfaces can be complicated by density-driven flows and the formation of stagnation zones, which inevitably introduces uncertainty into groundwater age-dating. While age-dating has proved effective to understand the seawater intrusion and aquifer salinization process in coastal aquifers, further efforts are needed to propagate model and data uncertainty to the uncertainty associated with the inferred age distributions. This study was performed in a coastal aquifer located close to the Yellow Sea, South Korea, where there is a decreasing trend of groundwater levels due to recent heavy exploitation, raising a warning of induced seawater intrusion. We inferred the groundwater age distributions in wells around the intrusion zone and estimated the uncertainty associated with the inference based on multiple age tracers including 3 H, tritiogenic 3 He, radiogenic 4 He, CFC-11, CFC-12 and CFC-113 using Bayesian inference. We examined various models representing the age distributions including traditional parametric Lumped Parameter Models (LPMs) and two non-parametric “shape-free” models. The results showed that the mean ages at the study site ranged from 10.9 to 522.5 y. Complex, multimodal distributions of ages occurred near a seawater intrusion area and upland recharge zones, implying converging paths of a wide range of different ages in those regions. In particular, the age distributions estimated near the seawater intrusion interface were characterized by heavy-tailed mixing structures with elevated concentrations of 4 He. This likely indicates density-driven upward flow at the seawater intrusion interface, forcing old groundwater rich in 4 He into the shallow aquifer. The Bayesian inference estimated large uncertainties particularly for the old age distributions, which was attributed partly to the gradual accumulation of 4 He in groundwater. The Bayesian inference improved understanding of flow dynamics at a complex seawater interface and identified opportunities to further reduce uncertainty of old water age estimates that characterize upwelling groundwater near the interface.

Jaancheon basin↗

USGS2010

The quality of our nation's waters: Nutrients in the nation's streams and groundwater, 1992-2004

National Findings and Their Implications Although the use of artificial fertilizer has supported increasing food production to meet the needs of a growing population, increases in nutrient loadings from agricultural and, to a lesser extent, urban sources have resulted in nutrient concentrations in many streams and parts of aquifers that exceed standards for protection of human health and (or) aquatic life, often by large margins. Do NAWQA findings substantiate national concerns for aquatic and human health? National Water-Quality Assessment (NAWQA) findings indicate that nutrient concentrations in streams and groundwater in basins with significant agricultural or urban development are substantially greater than naturally occurring or “background” levels. For example, median concentrations of total nitrogen and phosphorus in agricultural streams are about 6 times greater than background levels. Findings also indicate that concentrations in streams routinely were 2 to 10 times greater than regional nutrient criteria recommended by the U.S. Environmental Protection Agency (USEPA) to protect aquatic life. Such large differences in magnitude suggest that significant reductions in sources of nutrients, as well as greater use of land management strategies to reduce the transport of nutrients to streams, are needed to meet recommended criteria for streams draining areas with significant agricultural and urban development. Nitrate concentrations above the Federal drinking-water standard—or Maximum Contaminant Level (MCL)—of 10 milligrams per liter (mg/L, as nitrogen) are relatively uncommon in samples from streams used for drinking water or from relatively deep aquifers; the MCL is exceeded, however, in more than 20 percent of shallow (less than 100 feet below the water table) domestic wells in agricultural areas. This finding raises concerns for human health in rural agricultural areas where shallow groundwater is used for domestic supply and may warn of future contamination of deeper groundwater pumped from public‑supply wells. Are levels of nutrients in water increasing or decreasing? A decadal assessment of trends in concentrations of nitrogen and phosphorus from about 1993 to 2003 shows minimal changes in those concentrations in the majority of studied streams across the Nation, and more upward than downward trends in concentrations at sites with changes. These findings underscore the need for reductions in nutrient inputs or management strategies that would reduce transport of nutrients to streams. Upward trends were evident among all land uses, including those only minimally affected by agricultural and (or) urban development, which suggests that additional protection of some of our Nation’s most pristine streams warrants consideration. The median of nitrate concentrations in groundwater from 495 wells also increased significantly from 3.2 to 3.4 mg/L (6 percent) during about the same period, and the proportion of wells with concentrations of nitrate greater than the MCL increased from 16 to 21 percent. Nitrate concentrations in water in deep aquifers are likely to increase during the next decade as shallow groundwater with elevated concentrations moves downward. The potential for future contamination of the deep aquifers requires attention because these aquifers commonly are used for public water supply, and because restoration of groundwater is costly and difficult. Long-term and consistent monitoring of nutrients, improved accounting of nutrient sources, and improved tracking and modeling of climatic and landscape changes will be essential for distinguishing trends in nutrient concentrations, understanding the causes of those trends, and accurately tracking the effectiveness of strategies implemented to manage nutrients.

Circular↗

USGS2009

Simulation of Groundwater-Level and Salinity Changes in the Eastern Shore, Virginia

Groundwater-level and salinity changes have been simulated with a groundwater model developed and calibrated for the Eastern Shore of Virginia. The Eastern Shore is the southern part of the Delmarva Peninsula that is occupied by Accomack and Northampton Counties in Virginia. Groundwater is the sole source of freshwater to the Eastern Shore, and demands for water have been increasing from domestic, industrial, agricultural, and public-supply sectors of the economy. Thus, it is important that the groundwater supply be protected from overextraction and seawater intrusion. The best way for water managers to use all of the information available is usually to compile this information into a numerical model that can simulate the response of the system to current and future stresses. A detailed description of the geology, hydrogeology, and historical groundwater extractions was compiled and entered into the numerical model. The hydrogeologic framework is composed of a surficial aquifer under unconfined conditions, a set of three aquifers and associated overlying confining units under confined conditions (the upper, middle, and lower Yorktown-Eastover Formation), and an underlying confining unit (the St. Marys Formation). An estimate of the location and depths of two major paleochannels was also included in the framework of the model. Total withdrawals from industrial, commercial, public-supply, and some agricultural wells were compiled from the period 1900 through 2003. Reported pumpage from these sources increased dramatically during the 1960s and 70s, up to currently about 4 million gallons per day. Domestic withdrawals were estimated on the basis of population census districts and were assigned spatially to the model on the assumption that domestic users are located close to roads. A numerical model was created using the U.S. Geological Survey (USGS) code SEAWAT to simulate both water levels and concentrations of chloride (representing salinity). The model was calibrated using 605 predevelopment and transient water-level observations that are associated predominantly with 20 observation nests of wells sited across the study area. Sampling for groundwater chemistry at these sites revealed that chloride has not increased significantly in the last 20 years. Environmental tracers in the samples also indicated that the water in the surficial aquifer is typically years to decades old, whereas water in the confined aquifers is typically centuries to millennia old. The calibration procedure yielded distributions of hydraulic conductivity and storage coefficients of the aquifers and confining units that are based on 21 pilot points, but vary smoothly across the study area. The estimated values are consistent with other measurements of these properties measured previously on cores and during hydraulic tests at various well fields. Simulations performed with the model demonstrated that the calibrated model can reproduce the observed historical water levels fairly well (R2 = 0.93). The chloride concentrations were also simulated, but a match with chloride concentrations was more difficult to achieve (R2 = 0.16) because of the lack of sufficient data and the unknown exact behavior of the entire transition zone in the millennia leading up to the present day. Future pumping scenarios were simulated through 2050, with pumping set to either 2003 rates or total permitted withdrawal rates. Water levels in 2050 are predicted to be lower than current levels by a few feet where stresses are currently heaviest but potentially by tens of feet if total permitted withdrawals are extracted at current low-stressed sites. Simulations of chloride concentrations through 2050 revealed some potential for seawater intrusion in the areas of Cape Charles, Chincoteague, east of the town of Exmore, and east of the town of Accomac, but precise estimates of concentration increases are highly uncertain. Simulation results were also used to estimate that the down

Scientific Investigations Report↗

USGS2015

Hexavalent and total chromium at low reporting concentrations in source-water aquifers and surface waters used for public supply in Illinois, 2013

On the basis of their recent review of the human health effects of hexavalent chromium [Cr(VI)] in public drinking water, the U.S. Environmental Protection Agency is considering the need for Federal regulation of Cr(VI). Presently, only total chromium is regulated, at a Maximum Contaminant Level (MCL) of 100 micrograms per liter (µg/L). The occurrence of Cr(VI) in groundwater and surface waters generally is attributed to industrial sources, but can be of natural origin. California’s recently established MCL for Cr(VI) of 10 µg/L illustrates the drinking-water concerns associated with Cr(VI). To improve understanding of the possible impact of a Cr(VI)-specific standard that approximates the California level on the management of Illinois’ public drinking water, the U.S. Geological Survey, in cooperation with the Illinois Environmental Protection Agency, assessed the occurrence and distribution of Cr(VI) in the State’s public-water supplies. During 2013, untreated water samples were collected to be analyzed for Cr(VI) and total chromium [Cr(T)] at 119 water-supply wells and 32 surface-water intakes; also, 32 treated surface-water samples were collected near the point of treatment and 32 near the furthest point of distribution. Public-supply sample sites were selected by a stratified random method. Samples typically were analyzed within 24 hours of collection at reporting limits of 0.02 µg/L for Cr(VI) and 0.1 µg/L for Cr(T). The occurrence of Cr(VI) was compared with selected geophysical, physical, and sampling factors that might more fully explain its distribution and magnitude of concentrations. The maximum concentration of Cr(VI) in groundwater was 2.1 µg/L. Maximum concentrations in untreated and treated surface water were 0.29 µg/L and 2.4 µg/L, respectively. All sample concentrations were below the California MCL; only 35 percent were below that State’s non-enforceable public health goal of 0.02 of µg/L. Cr(VI) was undetected in 43 percent of untreated groundwater samples, with a median of 0.06 µg/L when detected. All but two (94 percent) of untreated surface-water samples had detections. In untreated surface water, the median concentration was 0.09 µg/L, whereas in treated (tap and distributed) water the median was 0.20 µg/L. Surface waters treated with lime for softening typically had the greatest Cr(VI) concentrations (maximum, 2.4 µg/L; median, 1.2 µg/L). The maximum concentration of Cr(T) in groundwater was 1.8 µg/L. Maximum concentrations in untreated and treated surface water were 1.8 µg/L and 2.5 µg/L, respectively. All sample concentrations were below the Federal MCL. Total chromium was detected in 65 percent of untreated groundwater samples, with a median of 0.40 µg/L, when detected. All but one (97 percent) of untreated surface-water samples had detections. In untreated surface water, the median concentration was 0.40 µg/L, whereas in treated (tap and distributed) water the median was 0.30 µg/L. As with Cr(VI), surface waters treated with lime typically had the greatest Cr(T) concentrations. Examination of factors that might account for or be associated with the occurrence of Cr(VI) in public-supply source waters found few clearly evident factors. Associations in frequencies of occurrence and range of concentrations indicate that surface waters and groundwaters of shallow, unconsolidated, unconfined aquifers, particularly alluvial aquifers, are possibly most commonly affected by anthropogenic sources of Cr(VI). Groundwaters of deep (greater than 500 feet) bedrock aquifers, particularly the Cambrian-Ordovician aquifer system, are possibly most commonly affected by geologic sources of Cr(VI). Additional study, with supporting geologic and geochemical data that were not collected in this study, would be necessary to verify these associations. There was a weak positive relation (ρ = 0.23) between concentrations of Cr(VI) and Cr(T) in untreated water samples, with a much stronger positive relation (ρ = 0.86 and ρ = 0.90, respectively) in samples collected soon after treatment and near the endpoint of distribution. The stronger relation and greater similarity between Cr(VI) and Cr(T) concentrations in treated water samples indicate that Cr(VI) represents a greater proportion of the measured concentrations of Cr(T) in treated waters than in untreated waters. The analysis of spikes and other quality-assurance samples indicate uncertainties associated with obtaining or confirming consistently accurate analytical results for Cr(VI) at near the applied reporting limit of 0.02 µg/L.

Illinois↗

USGS2015

Water quality of the Little Arkansas River and Equus Beds Aquifer before and concurrent with large-scale artificial recharge, south-central Kansas, 1995-2012

The city of Wichita artificially recharged about 1 billion gallons of water into the Equus Beds aquifer during 2007–2012 as part of Phase I recharge of the Artificial Storage and Recovery project. This report, prepared in cooperation by the U.S. Geological Survey and the city of Wichita, Kansas, summarizes Little Arkansas River (source-water for artificial recharge) and Equus Beds aquifer water quality before (1995–2006) and during (2007–2012) Artificial Storage and Recovery Phase I recharge. Additionally, aquifer water-quality distribution maps are presented and water-quality changes associated with Phase I recharge timing are described. Computed chloride concentrations in the Little Arkansas River exceeded the Federal secondary maximum contaminant level (SMCL) about 20 percent of the time during 1999 through 2012, primarily during low-flow conditions. Groundwater chloride concentrations during 2001 through 2012 exceeded the SMCL in about 6 percent of shallow wells and 7 percent of deep wells, primarily near Burrton, Kansas and along the Arkansas River. Nearly all surface water nitrate plus nitrite concentrations during 1995 through 2012 were less than the Federal maximum contaminant level (MCL); groundwater nitrate plus nitrite concentrations exceeded the MCL in about 16 percent of shallow groundwater samples and were minimal in the deeper parts of the aquifer. Several trace elements frequently exceeded drinking water criteria, including arsenic, iron, and manganese. Recharge activities at Phase I recharge wells have not resulted in substantial effects on groundwater quality in the area, likely because the total amount of water recharged is relatively small (1 billion gallons) compared to aquifer storage volume (greater than 990 billion gallons in winter 2012). The eastward movement of the Burrton chloride plume is likely being slowed by a line of recharge locations associated with Phase I; however, chloride concentrations in deep groundwater still advanced to less than one half mile from the central part of the study area. Water-quality constituents of concern (major ions, nutrients, trace elements, triazine herbicides, and fecal indicator bacteria) have not increased substantially and are likely more affected by climatological (natural recharge by precipitation) and natural (geochemical oxidation/reduction, metabolic and decay rates) processes than artificial recharge. Arsenic remains a water-quality constituent of concern because of natural and continued persistence of concentrations exceeding the Federal maximum contaminant level of 10 micrograms per liter, especially in the deeper parts of the Equus Beds aquifer.

Kansas↗

USGS1987

Ground-water-withdrawal and water-level data used to simulate regional flow in the major coastal plain aquifers of New Jersey

The report documents groundwater withdrawal and level data for the major aquifers of the New Jersey Coastal Plain. These data have been used in the Regional Aquifer System Analysis flow model of 10 major aquifers in the New Jersey Coastal Plain. Groundwater withdrawal data from more than 1,400 wells are tabulated by year for 1956 through 1980. Total yearly withdrawals for 171 public supply and industrial purveyors for 1918 through 1955 are documented. Best estimates are given for percentages of total withdrawals by aquifer for the 1918 through 1955 data. Groundwater withdrawal data is also tabulated yearly from 1918 through 1980 by county for each aquifer. Long-term hydrographs for 89 Coastal Plain wells provide information on water level fluctuations over time. Potentiometric maps showing earliest recorded water levels in Coastal Plain aquifers delineate prepumping conditions. Groundwater withdrawals from the Coastal Plain have increased from less than 50 million gal/day in 1918 to more than 350 million gal/day in 1980. In response to these increased withdrawals, groundwater levels have been steadily declining. In some areas where wells once flowed freely, water levels are now 100 to 200 ft below land surface. (USGS)

Water-Resources Investigations Report↗

USGS2015

Geochemical evolution of groundwater in the Mud Lake area, eastern Idaho, USA

Groundwater with elevated dissolved-solids concentrations—containing large concentrations of chloride, sodium, sulfate, and calcium—is present in the Mud Lake area of Eastern Idaho. The source of these solutes is unknown; however, an understanding of the geochemical sources and processes controlling their presence in groundwater in the Mud Lake area is needed to better understand the geochemical sources and processes controlling the water quality of groundwater at the Idaho National Laboratory. The geochemical sources and processes controlling the water quality of groundwater in the Mud Lake area were determined by investigating the geology, hydrology, land use, and groundwater geochemistry in the Mud Lake area, proposing sources for solutes, and testing the proposed sources through geochemical modeling with PHREEQC. Modeling indicated that sources of water to the eastern Snake River Plain aquifer were groundwater from the Beaverhead Mountains and the Camas Creek drainage basin; surface water from Medicine Lodge and Camas Creeks, Mud Lake, and irrigation water; and upward flow of geothermal water from beneath the aquifer. Mixing of groundwater with surface water or other groundwater occurred throughout the aquifer. Carbonate reactions, silicate weathering, and dissolution of evaporite minerals and fertilizer explain most of the changes in chemistry in the aquifer. Redox reactions, cation exchange, and evaporation were locally important. The source of large concentrations of chloride, sodium, sulfate, and calcium was evaporite deposits in the unsaturated zone associated with Pleistocene Lake Terreton. Large amounts of chloride, sodium, sulfate, and calcium are added to groundwater from irrigation water infiltrating through lake bed sediments containing evaporite deposits and the resultant dissolution of gypsum, halite, sylvite, and bischofite.

Idaho↗

USGS2000

Mechanism and rate of denitrification in an agricultural watershed: Electron and mass balance along groundwater flow paths

The rate and mechanism of nitrate removal along and between groundwater flow paths were investigated using a series of well nests screened in an unconfined sand and gravel aquifer. Intensive agricultural activity in this area has resulted in nitrate concentrations in groundwater often exceeding drinking water standards. Both the extent and rate of denitrification varied depending on the groundwater flow path. While little or no denitrification occurred in much of the upland portions of the aquifer, a gradual redox gradient is observed as aerobic upland groundwater moves deeper in the aquifer. In contrast, a sharp shallow redox gradient is observed adjacent to a third‐order stream as aerobic groundwater enters reduced sediments. An essentially complete loss of nitrate concurrent with increases in excess N 2 provide evidence that denitrification occurs as groundwater enters this zone. Electron and mass balance calculations suggest that iron sulfide (e.g., pyrite) oxidation is the primary source of electrons for denitrification. Denitrification rate estimates were based on mass balance calculations using nitrate and excess N 2 coupled with groundwater travel times. Travel times were determined using a groundwater flow model and were constrained by chlorofluorocarbon‐based age dates. Denitrification rates were found to vary considerably between the two areas where denitrification occurs. Denitrification rates in the deep, upland portions of the aquifer were found to range from <0.01 to 0.14 m M of N per year; rates at the redoxcline along the shallow flow path range from 1.0 to 2.7 m M of N per year. Potential denitrification rates in groundwater adjacent to the stream may be much faster, with rates up to 140 m M per year based on an in situ experiment conducted in this zone.

Water Resources Research↗

USGS1996

Age dating of shallow groundwater with chlorofluorocarbons, tritium/helium: 3, and flow path analysis, southern New Jersey coastal plain

Groundwater age dating through the combination of transient tracer methods (chlorofluorocarbons (CFCs) and tritium/helium 3 ( 3 H/ 3 He)) and groundwater flow path analysis is useful for investigating groundwater travel times, flow patterns, and recharge rates, as demonstrated by this study of the homogeneous shallow, unconfined Kirkwood-Cohansey aquifer system in the southern New Jersey coastal plain. Water samples for age dating were collected from three sets of nested observation wells (10 wells) with 1.5-m-long screens located near groundwater divides. Three steady state finite difference groundwater flow models were calibrated by adjusting horizontal and vertical hydraulic conductivities to match measured heads and head differences (range, 0.002–0.23 m) among the nested wells, with a uniform recharge rate of 0.46 m per year and porosities of 0.35 (sand) and 0.45 (silt) that were assumed constant for all model simulations and travel time calculations. The simulated groundwater travel times increase with depth in the aquifer, ranging from about 1.5 to 6.5 years for the shallow wells (screen bottoms 3–4 m below the water table), from about 10 to 25 years for the medium-depth wells (screen bottoms 8–19 m below the water table), and from about 30 to more than 40 years for the deep wells (screen bottoms 24–26 m below the water table). Apparent groundwater ages based on CFC- and 3 H/ 3 He-dating techniques and model-based travel times could not be statistically differentiated, and all were strongly correlated with depth. Confinement of 3He was high because of the rapid vertical flow velocity (of the order of 1 m/yr), resulting in clear delineation of groundwater travel times based on the 3 H/ 3 He-dating technique. The correspondence between the 3 H/ 3 He and CFC ages indicates that dispersion has had a minimal effect on the tracer-based ages of water in this aquifer. Differences between the tracer-based apparent ages for seven of the 10 samples were smaller than the error values. A slight bias toward older apparent ages, found not to be statistically significant, was noted for the 3 H/ 3 He-dating technique relative to the CFC-dating technique. This result may be caused by enrichment of local air in CFC-Il and CFC-12 from urban and industrial sources in the northeastern United States and minor contamination from sampling equipment. The demonstrated validity of the combined tracer-dating techniques to determine the age of water in the Kirkwood-Cohansey aquifer system indicates that groundwater flow models can be refined when apparent ages based on 3 H/ 3 He- and CFC- dating are used as calibration targets.

New Jersey↗

USGS2009

Geologic Setting and Hydrogeologic Units of the Columbia Plateau Regional Aquifer System, Washington, Oregon, and Idaho

The Columbia Plateau Regional Aquifer System (CPRAS) covers approximately 44,000 square miles of northeastern Oregon, southeastern Washington, and western Idaho. The area supports a $6 billion per year agricultural industry, leading the Nation in production of apples and nine other commodities (State of Washington Office of Financial Management, 2007; U.S. Department of Agriculture, 2007). Groundwater availability in the aquifers of the area is a critical water-resource management issue because the water demand for agriculture, economic development, and ecological needs is high. The primary aquifers of the CPRAS are basalts of the Columbia River Basalt Group (CRBG) and overlying basin-fill sediments. Water-resources issues that have implications for future groundwater availability in the region include (1) widespread water-level declines associated with development of groundwater resources for irrigation and other uses, (2) reduction in base flow to rivers and associated effects on temperature and water quality, and (3) current and anticipated effects of global climate change on recharge, base flow, and ultimately, groundwater availability. As part of a National Groundwater Resources Program, the U.S. Geological Survey began a study of the CPRAS in 2007 with the broad goals of (1) characterizing the hydrologic status of the system, (2) identifying trends in groundwater storage and use, and (3) quantifying groundwater availability. The study approach includes documenting changes in the status of the system, quantifying the hydrologic budget for the system, updating the regional hydrogeologic framework, and developing a groundwater-flow simulation model for the system. The simulation model will be used to evaluate and test the conceptual model of the system and later to evaluate groundwater availability under alternative development and climate scenarios. The objectives of this study were to update the hydrogeologic framework for the CPRAS using the available geologic mapping and well information and to develop a digital, three-dimensional hydrogeologic model that could be used as the basis of a groundwater-flow model. This report describes the principal geologic and hydrogeologic units of the CPRAS and geologic map and well data that were compiled as part of the study. The report also describes simplified regional hydrogeologic sections and unit extent maps that were used to conceptualize the framework prior to development of the digital 3-dimensional framework model.

Idaho, Oregon, Washington↗

USGS2012

Groundwater quality and simulation of sources of water to wells in the Marsh Creek valley at the U.S. Geological Survey Northern Appalachian Research Laboratory, Tioga County, Pennsylvania

This report provides a November 2010 snapshot of groundwater quality and an analysis of the sources of water to wells at the U.S. Geological Survey (USGS) Northern Appalachian Research Laboratory (NARL) near Wellsboro, Pennsylvania. The laboratory, which conducts fisheries research, currently (2011) withdraws 1,000 gallons per minute of high-quality groundwater from three wells completed in the glacial sand and gravel aquifer beneath the Marsh Creek valley; a fourth well that taps the same aquifer provides the potable supply for the facility. The study was conducted to document the source areas and quality of the water supply for this Department of Interior facility, which is surrounded by the ongoing development of natural gas from the Marcellus Shale. Groundwater samples were collected from the four wells used by the NARL and from two nearby domestic-supply wells. The domestic-supply wells withdraw groundwater from bedrock of the Catskill Formation. Samples were analyzed for major ions, nutrients, trace metals, radiochemicals, dissolved gases, and stable isotopes of oxygen and hydrogen in water and carbon in dissolved carbonate to document groundwater quality. Organic constituents (other than hydrocarbon gases) associated with hydraulic fracturing and other human activities were not analyzed as part of this assessment. Results show low concentrations of all constituents. Only radon, which ranged from 980 to 1,310 picocuries per liter, was somewhat elevated. These findings are consistent with the pristine nature of the aquifer in the Marsh Creek valley, which is the reason the laboratory was sited at this location. The sources of water and areas contributing recharge to wells were identified by the use of a previously documented MODFLOW groundwater-flow model for the following conditions: (1) withdrawals of 1,000 to 3,000 gallons per minute from the NARL wells, (2) average or dry hydrologic conditions, and (3) withdrawals of 1,000 gallons per minute from a new well 3,500 feet to the southwest that was drilled to provide water for Marcellus gas-well operations. Results of simulations indicate that during average hydrologic conditions, infiltration from Straight Run, a tributary to Marsh Creek, provides nearly all the water to the NARL wells. During dry conditions, the areas contributing recharge expand such that Asaph Run contributes about half of the water to the NARL wells when withdrawals are 1,000 or 2,000 gallons per minute. The addition of a simulated withdrawal of 1,000 gallons per minute from the nearby new well does not substantially affect the sources of water captured by the NARL wells. These results are subject to some limitations. The water-quality samples represent a snapshot of groundwater chemistry for only one hydrologic condition; the concentrations of some constituents may change temporally. In addition, samples were collected and analyzed for hydrocarbon gases, but not organic constituents associated with hydraulic fracturing; additional sampling for these constituents would provide a more complete water-quality baseline. The sources contributing water to the NARL wells and the new well were simulated by use of a simplified one-layer model of the glacial sand and gravel aquifer for steady-state conditions that in reality are never achieved. Steady-state simulations of dry hydrologic conditions show that it is possible for the NARL wells to capture water from Asaph Run; however, maps of simulated groundwater time-of-travel indicate that a dry period of unusually long duration would be required. A better analysis could be done by recalibrating the groundwater-flow model with a finite-difference grid having multiple layers, cells smaller than the 200-foot by 200-foot cells used in this study, and transient stress periods.

Pennsylvania↗

USGS2013

Overview of groundwater quality in the Piceance Basin, western Colorado, 1946--2009

Groundwater-quality data from public and private sources for the period 1946 to 2009 were compiled and put into a common data repository for the Piceance Basin. The data repository is available on the web at http://rmgsc.cr.usgs.gov/cwqdr/Piceance/index.shtml. A subset of groundwater-quality data from the repository was compiled, reviewed, and checked for quality assurance for this report. The resulting dataset consists of the most recently collected sample from 1,545 wells, 1,007 (65 percent) of which were domestic wells. From those samples, the following constituents were selected for presentation in this report: dissolved oxygen, dissolved solids, pH, major ions (chloride, sulfate, fluoride), trace elements (arsenic, barium, iron, manganese, selenium), nitrate, benzene, toluene, ethylbenzene, xylene, methane, and the stable isotopic compositions of water and methane. Some portion of recharge to most of the wells for which data were available was derived from precipitation (most likely snowmelt), as indicated by δ2H [H2O] and δ18O[H2O] values that plot along the Global Meteoric Water Line and near the values for snow samples collected in the study area. Ninety-three percent of the samples were oxic, on the basis of concentrations of dissolved oxygen that were greater than or equal to 0.5 milligrams per liter. Concentration data were compared with primary and secondary drinking-water standards established by the U.S. Environmental Protection Agency. Constituents that exceeded the primary standards were arsenic (13 percent), selenium (9.2 percent), fluoride (8.4 percent), barium (4.1 percent), nitrate (1.6 percent), and benzene (0.6 percent). Concentrations of toluene, xylenes, and ethylbenzene did not exceed standards in any samples. Constituents that exceeded the secondary standard were dissolved solids (72 percent), sulfate (37 percent), manganese (21 percent), iron (16 percent), and chloride (10 percent). Drinking-water standards have not been established for methane, which was detected in 24 percent of samples. Methane concentrations were greater than or equal to 1 milligram per liter in 8.5 percent of samples. Methane isotopic data for samples collected primarily from domestic wells in Garfield County indicate that methane in samples with relative high methane concentrations were derived from both biogenic and thermogenic sources. Many of the constituents that exceeded standards, such as arsenic, fluoride, iron, and manganese, were derived from rock and sediment in aquifers. Elevated nitrate concentrations were most likely derived from human sources such as fertilizer and human or animal waste. Information about the geologic unit or aquifer in which a well was completed generally was not provided by data sources. However, limited data indicate that Quaternary deposits in Garfield and Mesa Counties, the Wasatch Formation in Garfield County, and the Green River Formation in Rio Blanco County had some of the highest median concentrations of selected constituents. Variations in concentration with depth could not be evaluated because of the general lack of well-depth and water-level data. Concentrations of several important constituents, such as arsenic, manganese, methane, and nitrate, were related to concentrations of dissolved oxygen. Concentrations of arsenic, manganese, and methane were significantly higher in groundwater with low dissolved-oxygen concentrations than in groundwater with high dissolved-oxygen concentrations. In contrast, concentrations of nitrate were significantly higher in groundwater with high dissolved-oxygen concentrations than in groundwater with low dissolved-oxygen concentrations. These results indicate that measurements of dissolved oxygen may be a useful indicator of groundwater vulnerability to some human-derived contaminants and enrichment from some natural constituents. Assessing such a large and diverse dataset as the one available through the repository poses unique challenges for reporting on groundwater quality in the study area. The repository contains data from several studies that differed widely in purpose and scope. In addition to this variability in available data, gaps exist spatially, temporally, and analytically in the repository. For example, groundwater-quality data in the repository were not evenly distributed throughout the study area. Several key water-quality constituents or indicators, such as dissolved oxygen, were underrepresented in the repository. Ancillary information, such as well depth, depth to water, and the geologic unit or aquifer in which a well was completed, was missing for more than 50 percent of samples. Future monitoring could avoid several limitations of the repository by making relatively minor changes to sample- collection and data-reporting protocols. Field measurements for dissolved oxygen could be added to sampling protocols, for example. Information on well construction and the geologic unit or aquifer in which a well was completed should be part of the water-quality dataset. Such changes would increase the comparability of data from different monitoring programs and also add value to each program individually and to that of the regional dataset as a whole. Other changes to monitoring programs could require greater resources, such as sampling for a basic set of constituents that is relevant to major water-quality issues in the regional study area. Creation of such a dataset for the regional study area would help to provide the kinds of information needed to characterize background conditions and the spatial and temporal variability in constituent concentrations associated with those conditions. Without such information, it is difficult to identify departures from background that might be associated with human activities.

Colorado↗

USGS2013

Groundwater withdrawals 1976, 1990, and 2000--10 and land-surface-elevation changes 2000--10 in Harris, Galveston, Fort Bend, Montgomery, and Brazoria Counties, Texas

The study area comprising Harris County and parts of Galveston, Fort Bend, Montgomery, and Brazoria Counties in southeastern Texas forms part of one of the largest areas of land-surface-elevation change in the United States. Land-surface-elevation change in the study area primarily is caused by the withdrawal of groundwater. Groundwater withdrawn from the Chicot and Evangeline aquifers has been the primary source of water for municipal supply, industrial and commercial use, and irrigation in the study area. Groundwater withdrawals cause compaction of clay and silt layers abundant in the aquifers, which has in turn resulted in the widespread, substantial land-surface-elevation changes in the region with increased flooding. To estimate land-surface-elevation changes, the U.S. Geological Survey (USGS), in cooperation with the Harris-Galveston Subsidence District (HGSD), documented land-surface-elevation changes in the study area that occurred during 2000–10 and 2005–10 based on elevation data measured by 11 USGS borehole-extensometer sites, a National Geodetic Survey Continuously Operating Reference Station, and Global Positioning System Port-A-Measure (PAM) sites operated by the HGSD and the Fort Bend Subsidence District. Groundwater withdrawals in the study area also were documented for 1976, 1990, and 2000–10. In 1976, about 428.9 million gallons per day (Mgal/d) were withdrawn from the aquifer system in Harris County, but by 2000, because of HGSD regulation, withdrawals had decreased to about 337.8 Mgal/d, or about a 21-percent reduction since 1976. By 2010, withdrawals had decreased to about 227.1 Mgal/d, or about a 47-percent reduction since 1976. Among the counties in the study area, the largest decrease in groundwater withdrawals has occurred in Galveston County since 1976. In 1976, about 27.4 Mgal/d were withdrawn from the aquifer system, and by 2000, withdrawals had decreased to about 4.12 Mgal/d, or about an 85-percent reduction since 1976. By 2010, withdrawals had decreased to about 0.626 Mgal/d, or about a 98-percent decrease since 1976. Since the mid-1970s, Fort Bend and Montgomery Counties have undergone extensive urban development and corresponding large increases in groundwater withdrawals. Total groundwater withdrawal for Fort Bend County in 1976 was about 16.0 Mgal/d, and by 2000, withdrawals had increased to about 86.5 Mgal/d, or about a 441-percent increase since 1976. By 2010, withdrawals in Fort Bend County had increased to about 99.8 Mgal/d, or about a 524-percent increase since 1976. Total groundwater withdrawal for Montgomery County in 1976 was about 7.84 Mgal/d, and by 2000, withdrawals had increased to about 43.6 Mgal/d, or about a 456-percent increase since 1976. By 2010, withdrawals in Montgomery County had increased to about 64.2 Mgal/d, or about a 719-percent increase since 1976. Total groundwater withdrawal in Brazoria County in 1976 was about 18.0 Mgal/d, and by 2000, withdrawals had increased to about 26.0 Mgal/d, or about a 44-percent increase. By 2010, withdrawals in Brazoria County had increased to about 24.7 Mgal/d, or about a 37-percent increase since 1976. Measured land-surface-elevation changes from December 31, 2000, to December 31, 2010, ranged from an elevation increase of 0.06 feet (ft), or an average increase in elevation of 0.006 ft per year, at the Seabrook borehole extensometer located near Seabrook, Tex., to an elevation decrease of 1.28 ft, or an average decrease in elevation of 0.128 ft per year, at a PAM station north of Jersey Village, Tex. (PAM 07). Measured land-surface-elevation changes from December 31, 2005, to December 31, 2010, ranged from an elevation increase of 0.07 ft, or an average increase in elevation of 0.014 ft per year, at PAM 09 in far northeastern Harris County to an elevation decrease of 0.51 ft, or an average decrease in elevation of 0.102 ft per year, at PAM 07.

Texas↗

USGS2015

Simulation of groundwater flow and chloride transport in the “1,200-foot” sand with scenarios to mitigate saltwater migration in the “2,000-foot” sand in the Baton Rouge area, Louisiana

Groundwater withdrawals have caused saltwater to encroach into freshwater-bearing aquifers beneath Baton Rouge, Louisiana. The 10 aquifers beneath the Baton Rouge area, which includes East and West Baton Rouge Parishes, Pointe Coupee Parish, and East and West Feliciana Parishes, provided about 184.3 million gallons per day (Mgal/d) for public supply and industrial use in 2012. Groundwater withdrawals from the “1,200-foot” sand in East Baton Rouge Parish have caused water-level drawdown as large as 177 feet (ft) north of the Baton Rouge Fault and limited saltwater encroachment from south of the fault. The recently developed groundwater model for simulating transport in the “2,000-foot” sand was rediscretized to also enable transport simulation within the “1,200-foot” sand and was updated with groundwater withdrawal data through 2012. The model was recalibrated to water-level observation data through 2012 with the parameter-estimation code PEST and calibrated to observed chloride concentrations at observation wells within the “1,200-foot” sand and “2,000-foot” sand. The model is designed to evaluate strategies to control saltwater migration, including changes in the distribution of groundwater withdrawals and installation of scavenger wells to intercept saltwater before it reaches existing production wells. Seven hypothetical scenarios predict the effects of different groundwater withdrawal options on groundwater levels and the transport of chloride within the “1,200-foot” sand and the “2,000-foot” sand during 2015–2112. The predicted water levels and concentrations for all scenarios are depicted in maps for the years 2047 and 2112. The first scenario is a base case for comparison to the six other scenarios and simulates continuation of 2012 reported groundwater withdrawals through 2112 (100 years). The second scenario that simulates increased withdrawals from industrial wells in the “1,200-foot” sand predicts that water levels will be 12–25 ft lower by 2047 and that there will be a negligible difference in chloride concentrations within the “1,200-foot” sand. The five other scenarios simulate the effects of various withdrawal schemes on water levels and chloride concentrations within the “2,000-foot” sand. Amongst these five other scenarios, three of the scenarios simulate only various withdrawal reductions, whereas the two others also incorporate withdrawals from a scavenger well that is designed to extract salty water from the base of the “2,000-foot” sand. Two alternative pumping rates (2.5 Mgal/d and 1.25 Mgal/d) are simulated in each of the scavenger-well scenarios. For the “2,000-foot” sand scenarios, comparison of the predicted effects of the scenarios is facilitated by graphs of predicted chloride concentrations through time at selected observation wells, plots of salt mass in the aquifer through time, and a summary of the predicted plume area and average concentration. In all scenarios, water levels essentially equilibrate by 2047, after 30 years of simulated constant withdrawal rates. Although predicted water-level recovery within the “2,000-foot” sand is greatest for the scenario with the greatest reduction in groundwater withdrawal from that aquifer, the scavenger-well scenarios are most effective in mitigating the future extent and concentration of the chloride plume. The simulated scavenger-well withdrawal rate has more influence on the plume area and concentration than do differences among the scenarios in industrial and public-supply withdrawal rates.

Louisiana, Mississippi↗

USGS2014

Potentiometric surface and water-level difference maps of selected confined aquifers in Southern Maryland and Maryland’s Eastern Shore, 1975-2013

Groundwater is the principal source of freshwater supply in most of Southern Maryland and Maryland’s Eastern Shore. It is also the source of freshwater supply used in the operation of the Calvert Cliffs, Chalk Point, and Morgantown power plants. Increased groundwater withdrawals over the last several decades have caused groundwater levels to decline. This report presents potentiometric-surface maps of the Aquia and Magothy aquifers and the Upper Patapsco, Lower Patapsco, and Patuxent aquifer systems using water levels measured during September 2013. Water-level difference maps are also presented for four of these aquifers. The water-level differences in the Aquia aquifer are shown using groundwater-level data from 1982 and 2013, while the water-level differences are presented for the Magothy aquifer using data from 1975 and 2013. Water-level difference maps for both the Upper Patapsco and Lower Patapsco aquifer systems are presented using data from 1990 and 2013. The potentiometric surface maps show water levels ranging from 165 feet above sea level to 199 feet below sea level. Water levels have declined by as much as 113 feet in the Aquia aquifer since 1982, 81 feet in the Magothy aquifer since 1975, and 61 and 95 feet in the Upper Patapsco and Lower Patapsco aquifer systems, respectively, since 1990.

Maryland, Virginia↗

USGS2013

Sediment distribution and hydrologic conditions of the Potomac aquifer in Virginia and parts of Maryland and North Carolina

Sediments of the heavily used Potomac aquifer broadly contrast across major structural features of the Atlantic Coastal Plain Physiographic Province in eastern Virginia and adjacent parts of Maryland and North Carolina. Thicknesses and relative dominance of the highly interbedded fluvial sediments vary regionally. Vertical intervals in boreholes of coarse-grained sediment commonly targeted for completion of water-supply wells are thickest and most widespread across the central and southern parts of the Virginia Coastal Plain. Designated as the Norfolk arch depositional subarea, the entire sediment thickness here functions hydraulically as a single interconnected aquifer. By contrast, coarse-grained sediment intervals are thinner and less widespread across the northern part of the Virginia Coastal Plain and into southern Maryland, designated as the Salisbury embayment depositional subarea. Fine-grained intervals that are generally avoided for completion of water-supply wells are increasingly thick and widespread northward. Fine-grained intervals collectively as thick as several hundred feet comprise two continuous confining units that hydraulically separate three vertically spaced subaquifers. The subaquifers are continuous northward but merge southward into the single undivided Potomac aquifer. Lastly, far southeastern Virginia and northeastern North Carolina are designated as the Albemarle embayment depositional subarea, where both coarse- and fine-grained intervals are of only moderate thickness. The entire sediment thickness functions hydraulically as a single interconnected aquifer. A substantial hydrologic separation from overlying aquifers is imposed by the upper Cenomanian confining unit. Potomac aquifer sediments were deposited by a fluvial depositional complex spanning the Virginia Coastal Plain approximately 100 to 145 million years ago. Westward, persistently uplifted granite and gneiss source rocks sustained a supply of coarse-grained sand and gravel. Immature, high-gradient braided streams deposited longitudinal bars and channel fills across the Norfolk arch subarea. By contrast, across the Salisbury and Albemarle embayment subareas, mature, medium- to low-gradient meandering streams deposited medium- to coarse-grained channel fills and point bars segregated from fine-grained overbank deposits. The Virginia depositional complex merged northward across the Salisbury embayment subarea with another complex in Maryland. Here, additional sediments were received from schist source rocks that underwent three cycles of initial uplift and rapid erosion followed by crustal stability and erosional leveling. Because of the predominance of coarse-grained sediments, transmissivity, hydraulic conductivity, and regional velocities of lateral flow through the Potomac aquifer are greatest across the Norfolk arch depositional subarea, but decrease progressively northward with increasingly fine-grained sediments. Confining units hydraulically separate the Potomac aquifer from overlying aquifers, as indicated by large vertical hydraulic gradients. By contrast, most of the Potomac aquifer internally functions hydraulically as a single interconnected aquifer, as indicated by uniformly small vertical gradients. Most fine-grained sediments within the aquifer do not hydraulically separate overlying and underlying coarse-grained sediments. Across the Salisbury embayment depositional subarea, however, hydraulic separation among the vertically spaced subaquifers is imposed by the intervening confining units. The Potomac aquifer is the largest and most heavily used source of groundwater in the Virginia Coastal Plain. Water-level declines as great as 200 feet create the potential for saltwater intrusion. Conventional stratigraphic correlation has been generally ineffective at accurately characterizing complexly distributed fluvial sediments that compose the Potomac aquifer. Consequently, the aquifer’s internal hydraulic connectivity and overall hydrologic function have not been well understood. Water-supply planning and development efforts have been hampered, and interpretations of regulatory criteria for allowable water-level declines have been ambiguous. An investigation undertaken during 2010–11 by the U.S. Geological Survey, in cooperation with the Virginia Department of Environmental Quality, provides a comprehensive regional description of the spatial distribution of Potomac aquifer sediments and their relation to hydrologic conditions. Altitudes and thicknesses of 2,725 vertical sediment intervals represent the spatial distribution of Potomac aquifer sediments in the Virginia Coastal Plain and adjacent parts of Maryland and North Carolina. Sediment intervals are designated as either dominantly coarse or fine grained and were determined by interpretation of geophysical logs and ancillary information from 456 boreholes. Sediment-interval and borehole summary statistical data indicate regional trends in sediment lithology and stratigraphic continuity, upon which three structurally based and hydrologically distinct sediment depositional subareas are designated. Broad patterns of sediment deposition over time are inferred from published sediment pollen-age data. Discrepancies in previously drawn hydrostratigraphic relations between southeastern Virginia and northeastern North Carolina are partly resolved based on borehole geophysical logs and a recently documented geologic map and corehole. A conceptual model theorizes the depositional history of the sediments and geologically accounts for their distribution. Documented pumping tests of the Potomac aquifer at 197 locations produced 336 values of transmissivity and 127 values of storativity. Based on effective aquifer thicknesses, 296 values of sediment hydraulic conductivity and 113 values of sediment specific storage are calculated. Vertical hydraulic gradients are calculated from 9,479 pairs of water levels measured between November 17, 1953, and October 4, 2011, in 129 closely spaced pairs of wells. Borehole sediment-interval and related data provide a means to achieve high yielding production wells in the Potomac aquifer by site-specific targeting of drilling operations toward water-bearing coarse-grained sand and gravel. Advance knowledge of the potential of different parts of the aquifer also aids in planning optimal groundwater-development areas. Depositional subareas further provide a possible context for resource management. Current (2013) regulatory limits on water-level declines are relative to top surfaces of subdivided upper, middle, and lower Potomac aquifers across the entire Virginia Coastal Plain, but have the potential to exceed the same limit relative to a single undivided Potomac aquifer. By contrast, designation of the sediments as a single aquifer in the Norfolk arch and Albemarle embayment subareas—and as a series of vertically spaced subaquifers and intervening confining units in the Salisbury embayment subarea—best reflects understanding of the Potomac aquifer and can avoid the potential for excessive water-level declines. Simulation modeling to evaluate effects of groundwater withdrawals could be designed similarly, including vertical discretization and (or) zonation of the Potomac aquifer based on depositional subareas and a geostatistical distribution of aquifer properties derived from borehole sediment-interval data. Further resource-management information needs extend beyond the developed part of the Potomac aquifer, particularly across the Northern Neck and Middle Peninsula where only the shallowest part of the aquifer is known, and include structural aspects such as faults, basement bedrock, and the Chesapeake Bay impact crater.

Maryland, North Carolina, Virginia↗

USGS2017

Hydrology of the Claiborne aquifer and interconnection with the Upper Floridan aquifer in southwest Georgia

The U.S. Geological Survey conducted a study, in cooperation with the Georgia Environmental Protection Division, to define the hydrologic properties of the Claiborne aquifer and evaluate its connection with the Upper Floridan aquifer in southwest Georgia. The effort involved collecting and compiling hydrologic data from the aquifer in subarea 4 of southwestern Georgia. Data collected for this study include borehole geophysical logs in 7 wells, and two 72-hour aquifer tests to determine aquifer properties. The top of the Claiborne aquifer extends from an altitude of about 200 feet above the North American Vertical Datum of 1988 (NAVD 88) in Terrell County to 402 feet below NAVD 88 in Decatur County, Georgia. The base of the aquifer extends from an altitude of about 60 feet above NAVD 88 in eastern Sumter County to about 750 feet below NAVD 88 in Decatur County. Aquifer thickness ranges from about 70 feet in eastern Early County to 400 feet in Decatur County. The transmissivity of the Claiborne aquifer, determined from two 72-hour aquifer tests, was estimated to be 1,500 and 700 feet squared per day in Mitchell and Early Counties, respectively. The storage coefficient was estimated to be 0.0006 and 0.0004 for the same sites, respectively. Aquifer test data from Mitchell County indicate a small amount of leakage occurred during the test. Groundwater-flow models suggest that the source of the leakage was the underlying Clayton aquifer, which produced about 2.5 feet of drawdown in response to pumping in the Claiborne aquifer. The vertical hydraulic conductivity of the confining unit between the Claiborne and Clayton aquifers was simulated to be about 0.02 foot per day. Results from the 72-hour aquifer tests run for this study indicated no interconnection between the Claiborne and overlying Upper Floridan aquifers at the two test sites. Additional data are needed to monitor the effects that increased withdrawals from the Claiborne aquifer may have on future water resources.

Georgia↗