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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.

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At least 1,459 records · Page 81Linked to original sources

USGS1993

Geohydrology and water quality of the Calumet aquifer, in the vicinity of the Grand Calumet River/Indiana Harbor Canal, northwestern Indiana

The water-table configuration of the Calumet aquifer in the vicinity of the Grand Calumet River/Indiana Harbor Canal in Lake County, northwestern Indiana, reflects the complexity of the shallow ground-water-flow system. Large depressions in the water table in sewered areas interrupt broad ground-water divides between rivers. The aquifer/stream interactions along the Grand Calumet River/ Indiana Harbor Canal are directly related to Lake Michigan water levels because of a direct connection of the Grand Calumet River/Indiana Harbor Canal to the lake. Fluctuations in lake levels and evapotranspiration result in reversals in ground-water flow near the river and canal that last from several hours to several months. Most of the water from the Calumet aquifer discharges into sewers, the Grand Calumet River/Indiana Harbor Canal, Lake Michigan, and Silurian carbonate bedrock. Model simulations of ground-water flow for the study area indicate that the Calumet aquifer discharges about 15 ft 3 /s (cubic feet per second) of ground water to sewers, about 10 ft 3 /s to the Grand Calumet River/Indiana Harbor Canal, and about 4 ft 3 /s to Lake Michigan along a 25-mile section of shoreline. Estimates of groundwater flow from the Calumet aquifer to the bedrock range from 0 to 10 ft 3 /s. Results of analyses of water samples collected from wells in five land-use types steel industry, petrochemical industry, commercial and light industry, residential, and parks were compared. The highest median concentrations of inorganic ions and the most detections of organic compounds generally occurred in water samples from wells on the steel and petrochemical land-use areas. Water samples collected from wells on the commercial and light industrial land-use areas generally had lower median chemical concentrations than the samples from the steel and petrochemical land-use areas and greater median concentrations than the samples from the residential and park land-use areas. Seven of 52 acid-extractable and base/neutralextractable organic compounds and 17 of 36 volatile organic compounds analyzed were detected in a total of 35 wells. Only 4 of the 88 organic analytes phenols, bis(2-ethylhexyl)phthalate, benzene, and toluene were detected in more than 5 of the 35 wells. A comparison of primarily inorganic-constituent data from the five land-use groups to inorganic-constituent data from sites known to be contaminated shows that constituent concentrations in ground waters from wells in the land-use areas generally are lower than those in ground water from contaminated areas. Abstract 1 Likewise, a comparison of inorganic-constituent data from the land-use groups to inorganic-constituent data from areas relatively unaffected by human presence shows that constituent concentrations in ground water from wells in the land-use areas generally are greater than those in ground water from the unaffected areas. Some documented but unaccounted for chemical loads in the Grand Calumet River are from ground water. Ground water probably contributes more than 10 percent of the total chemical load of ammonia, chromium, and cyanide to the Grand Calumet River. In comparison, about 1 to 3 percent of the total streamflow in the Grand Calumet River is from ground water. Of the four major groundwater sinks in the aquifer, the east branch of the Grand Calumet River and the Indiana Harbor Canal generally receive the greatest chemical loads from ground water, whereas Lake Michigan generally receives the smallest loads.

Indiana↗

USGS2004

Aquifer vulnerability to pesticide pollution: Combining soil, land-use and aquifer properties with molecular descriptors

This study uses an extensive survey of herbicides in groundwater across the midwest United States to predict occurrences of a range of compounds across the region from a combination of their molecular properties and the properties of the catchment of a borehole. The study covers 100 boreholes and eight pesticides. For each of the boreholes its catchment the soil, land-use and aquifer properties were characterized. Discriminating boreholes where pollution occurred from those where no pollution occurred gave a model that was 74% correct with organic carbon content, percentage sand content and depth to the water table being significant properties of the borehole catchment. Molecular topological descriptors as well as K oc , solubility and half-life were used to characterize each compound included in the study. Inclusion of molecular properties makes it possible to discriminate between occurrence and non-occurrence of each compound in each well. The best-fit model combines: organic carbon content, percentage sand content and depth to the water table with molecular descriptors representing molecular size, molecular branching and functional group composition of the herbicides.

Midwest region↗

USGS1977

Water table in the surficial aquifer and potentiometric surface of the Floridan Aquifer in selected well fields, west-central Florida, May 1977

The coastal parts of Pasco, Pinellas and Hillsborough are undergoing extensive urban development. The Floridan aquifer is the area 's principal water supply. Potentiometric and water-table maps were prepared in order to determine the effect of groundwater withdrawals in selected well fields in west-central Florida. These maps were prepared in May 1977 to capture the annual low-water-level period. Declines in the potentiometric surface ranged from 3 feet in the Starkey well field to 25 feet in the Sun City well field. (Woodard-USGS)

Open-File Report↗

USGS2014

Uncertainty analysis of a groundwater flow model in east-central Florida

A groundwater flow model for east-central Florida has been developed to help water-resource managers assess the impact of increased groundwater withdrawals from the Floridan aquifer system on heads and spring flows originating from the Upper Floridan aquifer. The model provides a probabilistic description of predictions of interest to water-resource managers, given the uncertainty associated with system heterogeneity, the large number of input parameters, and a nonunique groundwater flow solution. The uncertainty associated with these predictions can then be considered in decisions with which the model has been designed to assist. The “Null Space Monte Carlo” method is a stochastic probabilistic approach used to generate a suite of several hundred parameter field realizations, each maintaining the model in a calibrated state, and each considered to be hydrogeologically plausible. The results presented herein indicate that the model’s capacity to predict changes in heads or spring flows that originate from increased groundwater withdrawals is considerably greater than its capacity to predict the absolute magnitudes of heads or spring flows. Furthermore, the capacity of the model to make predictions that are similar in location and in type to those in the calibration dataset exceeds its capacity to make predictions of different types at different locations. The quantification of these outcomes allows defensible use of the modeling process in support of future water-resources decisions. The model allows the decision-making process to recognize the uncertainties, and the spatial/temporal variability of uncertainties that are associated with predictions of future system behavior in a complex hydrogeological context.

Florida↗

USGS2018

Calibration of regional hydraulic and transport properties of an arid-region aquifer under modern and paleorecharge conditions using water levels and environmental tracers

A two-dimensional numerical groundwater flow model was established and calibrated for the hyperarid Najd region in southern Oman. The results indicate that recent recharge rates are required to sustain the observed groundwater heads in the Najd. The model was also used to estimate possible ranges of past recharge rates and the effective porosity of the main aquifer unit. Recharge rates during past humid periods were estimated to be no more than 1–3 times modern rates. The effective porosity was estimated to be between 0.06 and 0.093. Insight into the nature of the long-term transport within the aquifer was gained by using transient model runs over the last 350 ka and (1) varying the recharge intensity (from 0.1 to 2.5 times modern), and (2) the timing and duration of humid and dry periods. Finally, results indicate that although recharge rates and the flow conditions have likely changed over time, a steady-state model is capable of reproducing the observed groundwater residence times in the Najd based on carbon-14, helium and chlorine-36 dating.

Hydrogeology Journal↗

USGS2024

Imaging freshwater and saline aquifers beneath Bradford County, Pennsylvania, USA, using Audio-Magnetotelluric (AMT) data

We investigate the utility of audio-magnetotelluric (AMT) data for detecting high electrical conductivity zones indicative of fresh and saline groundwater lenses at depths of < ∼1000 m at seven survey sites in the southwestern corner of Bradford County, PA. Dimensionality analysis indicates the AMT data can be interpreted using two-dimensional (2-D) models. 2-D electrical resistivity models obtained from inverting the AMT data reveal conductive zones at depths of <30 m at all sites, between depths of 50–150 m at six sites, and between depths of 400–600 m at one site. The models show slightly lower resistivities (∼15–30 Ω m) in the deeper zones compared to the shallower zones (>30 Ω m). Consistent with well log data from two boreholes in the study area and salinity estimates obtained from the imaged resistivities, we interpret the <30 m deep conductive zone as the freshwater aquifer, and the two deeper conductive zones as salty/briny groundwater lenses. Our salinity estimates for the deeper zones vary from 1 to 380 (unitless Practical Salinity Scale), which agrees well with previous estimates of Appalachian brine salinity of 10–343. We attribute the high-salinity groundwater lenses to Appalachian Basin brine migrating upwards from deeper in the basin via bedrock fracture and fault systems. Our findings indicate AMT surveying can be useful for imaging fresh and saline aquifers at shallow depths (< ∼1000 m), at least within the northeastern section of the Appalachian Basin in Pennsylvania.

Pennsylvania↗

USGS2022

Predicting regional fluoride concentrations at public and domestic supply depths in basin-fill aquifers of the western United States using a random forest model

A random forest regression (RFR) model was applied to over 12,000 wells with measured fluoride (F) concentrations in untreated groundwater to predict F concentrations at depths used for domestic and public supply in basin-fill aquifers of the western United States. The model relied on twenty-two regional-scale environmental and surficial predictor variables selected to represent factors known to control F concentrations in groundwater. The testing model fit R 2 and RMSE were 0.52 and 0.78 mg/L. Comparisons of measured to predicted proportions of four F-concentrations categories (<0.7 mg/L, 0.7–2 mg/L, >2 mg/L – 4 mg/L, and > 4 mg/L) indicate that the model performed well at making regional-scale predictions. Differences between measured and predicted proportions indicate underprediction of measured F at values by between 4 and 20 mg/L, representing less than 1% of the regional scale predicted values. These residuals most often map to geographic regions where local-scale processes including evaporative discharge in closed basins or intermittent streams concentrate fluoride in shallow groundwater. Despite this, the RFR model provides spatially continuous F predictions across the basin-fill aquifers where discrete samples are missing. Further, the predictions capture documented areas that exceed the F maximum contaminant level for drinking water of 4 mg/L and areas that are below the oral-health benchmark of 0.7 mg/L. These predictions can be used to estimate fluoride concentrations in unmonitored areas and to aid in identifying geographic areas that may require further investigation at localized scales.

Arizona, California, Colorado, New Mexico, Nevada,↗

USGS2020

Occurrence and geochemistry of lead-210 and polonium-210 radionuclides in public-drinking-water supplies from principal aquifers of the United States

On the basis of lifetime cancer risks, lead-210 ( 210 Pb) and polonium-210 ( 210 Po) ≥ 1.0 and 0.7 pCi/L (picocuries per liter), respectively, in drinking-water supplies may pose human-health concerns. 210 Pb and 210 Po were detected at concentrations greater than these thresholds at 3.7 and 1.5%, respectively, of filtered untreated groundwater samples from 1263 public-supply wells in 19 principal aquifers across the United States. Nationally, 72% of samples with radon-222 ( 222 Rn) concentrations > 4000 pCi/L had 210 Pb ≥ 1.0 pCi/L. 210 Pb is mobilized by alpha recoil associated with the decay of 222 Rn and short-lived progeny. 210 Pb concentrations ≥ 1.0 pCi/L occurred most frequently where acidic groundwaters inhibited 210 Pb readsorption (felsic-crystalline rocks) and where reducing alkaline conditions favored dissolution of iron–manganese- (Fe–Mn-) oxyhydroxides (which adsorb 210 Pb) and formation of lead–carbonate complexes (enhancing lead (Pb) mobility). 210 Po concentrations ≥ 0.7 pCi/L occurred almost exclusively in confined Coastal Plain aquifers where old (low percent-modern carbon-14) groundwaters were reducing, with high pH (>7.5) and high sodium/chloride (Na/Cl) ratios resulting from cation exchange. In high-pH environments, aqueous polonium (Po) is poorly sorbed, occurring as dihydrogen polonate (H 2 PoO 3 (aq)) or, under strongly reducing conditions, as a hydrogen-polonide anion (HPo – ). Fe–Mn- and sulfate-reduction and cation-exchange processes may mobilize polonium from mineral surfaces. Po 2+ occurrence in low-to-neutral-pH waters is attenuated by adsorption.

Environmental Science Technology↗

USGS2019

Hormones and pharmaceuticals in groundwater used as a source of drinking water across the United States

This is the first large-scale, systematic assessment of hormone and pharmaceutical occurrence in groundwater used for drinking across the United States. Samples from 1091 sites in Principal Aquifers representing 60% of the volume pumped for drinking-water supply had final data for 21 hormones and 103 pharmaceuticals. At least one compound was detected at 5.9% of 844 sites representing the resource used for public supply across the entirety of 15 Principal Aquifers, and at 11.3% of 247 sites representing the resource used for domestic supply over subareas of nine Principal Aquifers. Of 34 compounds detected, one plastics component (bisphenol A), three pharmaceuticals (carbamazepine, sulfamethoxazole, and meprobamate), and the caffeine degradate 1,7-dimethylxanthine were detected in more than 0.5% of samples. Hydrocortisone had a concentration greater than a human-health benchmark at 1 site. Compounds with high solubility and low K oc were most likely to be detected. Detections were most common in shallow wells with a component of recent recharge, particularly in crystalline-rock and mixed land-use settings. Results indicate vulnerability of groundwater used for drinking water in the U.S. to contamination by these compounds is generally limited, and exposure to these compounds at detected concentrations is unlikely to have adverse effects on human health.

Environmental Science & Technology↗

USGS2009

Fate of sulfamethoxazole, 4-nonylphenol, and 17β-estradiol in groundwater contaminated by wastewater treatment plant effluent

Organic wastewater contaminants (OWCs) were measured in samples collected from monitoring wells located along a 4.5-km transect of a plume of groundwater contaminated by 60 years of continuous rapid infiltration disposal of wastewater treatment plant effluent. Fifteen percent of the 212 OWCs analyzed were detected, including the antibiotic sulfamethoxazole (SX), the nonionic surfactant degradation product 4-nonylphenol (NP), the solvent tetrachloroethene (PCE), and the disinfectant 1,4-dichlorobenzene (DCB). Comparison of the 2005 sampling results to data collected from the same wells in 1985 indicates that PCE and DCB are transported more rapidly in the aquifer than NP, consistent with predictions based on compound hydrophobicity. Natural gradient in situ tracer experiments were conducted to evaluate the subsurface behavior of SX, NP, and the female sex hormone 17β-estradiol (E2) in two oxic zones in the aquifer: (1) a downgradient transition zone at the interface between the contamination plume and the overlying uncontaminated groundwater and (2) a contaminated zone located beneath the infiltration beds, which have not been loaded for 10 years. In both zones, breakthrough curves for the conservative tracer bromide (Br − ) and SX were nearly coincident, whereas NP and E2 were retarded relative to Br − and showed mass loss. Retardation was greater in the contaminated zone than in the transition zone. Attenuation of NP and E2 in the aquifer was attributed to biotransformation, and oxic laboratory microcosm experiments using sediments from the transition and contaminated zones show that uniform-ring-labeled 14 C 4-normal-NP was biodegraded more rapidly (30−60% recovered as 14 CO 2 in 13 days) than 4- 14 C E2 (20−90% recovered as 14 CO 2 in 54 days). There was little difference in mineralization potential between sites.

Massachusetts↗

USGS1998

Molybdate transport in a chemically complex aquifer: Field measurements compared with solute-transport model predictions

A natural-gradient tracer test was conducted in an unconfined sand and gravel aquifer on Cape Cod, Massachusetts. Molybdate was included in the injectate to study the effects of variable groundwater chemistry on its aqueous distribution and to evaluate the reliability of laboratory experiments for identifying and quantifying reactions that control the transport of reactive solutes in groundwater. Transport of molybdate in this aquifer was controlled by adsorption. The amount adsorbed varied with aqueous chemistry that changed with depth as freshwater recharge mixed with a plume of sewage-contaminated groundwater. Molybdate adsorption was strongest near the water table where p H (5.7) and the concentration of the competing solutes phosphate (2.3 micromolar) and sulfate (86 micromolar) were low. Adsorption of molybdate decreased with depth as p H increased to 6.5, phosphate increased to 40 micromolar, and sulfate increased to 340 micromolar. A one-site diffuse-layer surface-complexation model and a two-site diffuse-layer surface-complexation model were used to simulate adsorption. Reactions and equilibrium constants for both models were determined in laboratory experiments and used in the reactive-transport model PHAST to simulate the two-dimensional transport of molybdate during the tracer test. No geochemical parameters were adjusted in the simulation to improve the fit between model and field data. Both models simulated the travel distance of the molybdate cloud to within 10% during the 2-year tracer test; however, the two-site diffuse-layer model more accurately simulated the molybdate concentration distribution within the cloud.

Massachusetts↗

USGS2022

Improving gas-derived parameterization of groundwater using free phase gas measurements

Dissolved atmogenic gasses in groundwater provide significant information about recharge conditions, flowpath, and age. Free phase gas in aquifers is largely ignored in these analyses and there is a lack of quantitative analysis for gas flux mechanisms. Many related fields encountering multiphase flow acknowledge that the presence of bubbles allows for the rapid exsolution of dissolved gasses and volatile compounds through diffusive and polar forces. By measuring the mass flow of the exsolved gas at a spring, coupled with compositional analysis in the free and dissolved phases, we show that not incorporating the effects of the free gas phase of bubbling springs introduces error in the estimation of total gas quantities, particularly light noble gasses. This can significantly affect the corresponding estimation of noble gas temperature (NGT) and apparent age. We examine the transport of free and dissolved gas from the recharge zone, using water level variation data, to the discharge location where the gases are measured. This technique of using the free gas phase for assessing aquifer dynamics will improve groundwater conceptual models, particularly in karstic aquifers where rapid fluctuations in the water table facilitate the development of excess air, generating multiphase spring discharge.

Environmental Science: Water Research & Technology↗

USGS1988

Denitrification in a sand and gravel aquifer

Denitrification was assayed by the acetylene blockage technique in slurried core material obtained from a freshwater sand and gravel aquifer. The aquifer, which has been contaminated with treated sewage for more than 50 years, had a contaminant plume greater than 3.5-km long. Near the contaminant source, groundwater nitrate concentrations were greater than 1 mM, whereas 0.25 km downgradient the central portion of the contaminant plume was anoxic and contained no detectable nitrate. Samples were obtained along the longitudinal axis of the plume (0 to 0.25 km) at several depths from four sites. Denitrification was evident at in situ nitrate concentrations at all sites tested; rates ranged from 2.3 to 260 pmol of N 2 O produced (g of wet sediment) −1 h −1 . Rates were highest nearest the contaminant source and decreased with increasing distance downgradient. Denitrification was the predominant nitrate-reducing activity; no evidence was found for nitrate reduction to ammonium at any site. Denitrifying activity was carbon limited and not nitrate limited, except when the ambient nitrate level was less than the detection limit, in which case, even when amended with high concentrations of glucose and nitrate, the capacity to denitrify on a short-term basis was lacking. These results demonstrate that denitrification can occur in groundwater systems and, thereby, serve as a mechanism for nitrate removal from groundwater.

Massachusetts↗

USGS2012

Synoptic water-level measurements of the Upper Floridan aquifer in Florida and parts of Georgia, South Carolina, and Alabama, May-June 2010

Water levels for the Upper Floridan aquifer were measured throughout Florida and in parts of Georgia, South Carolina, and Alabama in May-June 2010. These measurements were compiled for the U.S. Geological Survey (USGS) Floridan Aquifer System Groundwater Availability Study and conducted as part of the USGS Groundwater Resources Program. Data were collected by personnel from the USGS Florida Water Science Center, Georgia Water Science Center, South Carolina Water Science Center and several state and county agencies in Florida, Georgia, South Carolina, and Alabama using standard techniques. Data collected by USGS personnel are stored in the USGS National Water Information System (NWIS), Groundwater Site-Inventory System (GWSI). Furnished records from cooperators are stored in NWIS/GWSI when possible, but are available from the source agency.

Alabama, Florida, Georgia, South Carolina↗

USGS2016

Groundwater contaminant science activities of the U.S. Geological Survey in New England

Aquifers in New England provide water for human needs and natural ecosystems. In some areas, however, aquifers have been degraded by contaminants from geologic and human sources. In recent decades, the U.S. Geological Survey has been a leader in describing contaminant occurrence in the bedrock and surficial aquifers of New England. In cooperation with Federal, State, and local agencies, the U.S. Geological Survey has also studied the vulnerability of groundwater to contaminants, the factors affecting the geographic distribution of contaminants, and the geochemical processes controlling contaminant transport and fate. This fact sheet describes some of the major science needs in the region related to groundwater contaminants and highlights recent U.S. Geological Survey studies that provide a foundation for future investigations.

New England↗

USGS2019

The Missouri groundwater-level observation network

The Missouri groundwater-level observation well network is a series of wells across the State of Missouri in which groundwater levels are monitored in real time and periodically. The wells monitor the water levels in multiple key aquifers, such as the Ozark aquifer in the Salem and Springfield Plateaus and the Mississippi Alluvial Plain aquifer in the South-eastern Lowlands. As of 2018, 150 real-time sites are operated as a cooperative effort between the Missouri Department of Natural Resources (MoDNR) and the U.S. Geological Survey. This fact sheet describes the network and well data from the network.

Missouri↗

USGS2012

Groundwater quality in the Upper Susquehanna River Basin, New York, 2009

Water samples were collected from 16 production wells and 14 private residential wells in the Upper Susquehanna River Basin from August through December 2009 and were analyzed to characterize the groundwater quality in the basin. Wells at 16 of the sites were completed in sand and gravel aquifers, and 14 were finished in bedrock aquifers. In 2004–2005, six of these wells were sampled in the first Upper Susquehanna River Basin study. Water samples from the 2009 study were analyzed for 10 physical properties and 137 constituents that included nutrients, organic carbon, major inorganic ions, trace elements, radionuclides, pesticides, volatile organic compounds, and 4 types of bacterial analyses. Results of the water-quality analyses are presented in tabular form for individual wells, and summary statistics for specific constituents are presented by aquifer type. The results are compared with Federal and New York State drinking-water standards, which typically are identical. The results indicate that groundwater genrally is of acceptable quality, although concentrations of some constituents exceeded at least one drinking-water standard at 28 of the 30 wells. These constituents include: pH, sodium, aluminum, manganese, iron, arsenic, radon-222, residue on evaporation, total and fecal coliform including Escherichia coli and heterotrophic plate count.

New York↗

USGS2012

Groundwater quality in the Genesee River Basin, New York, 2010

Water samples collected from eight production wells and eight private residential wells in the Genesee River Basin from September through December 2010 were analyzed to characterize the groundwater quality in the basin. Eight of the wells were completed in sand and gravel aquifers, and eight were finished in bedrock aquifers. Three of the 16 wells were sampled in the first Genesee River Basin study during 2005-2006. Water samples from the 2010 study were analyzed for 147 physiochemical properties and constituents that included major ions, nutrients, trace elements, radionuclides, pesticides, volatile organic compounds (VOCs), and indicator bacteria. Results of the water-quality analyses are presented in tabular form for individual wells, and summary statistics for specific constituents are presented by aquifer type. The results are compared with Federal and New York State drinking-water standards, which typically are identical. The results indicate that groundwater generally is of acceptable quality, although concentrations of the following constituents exceeded current or proposed Federal or New York State drinking-water standards at each of the 16 wells sampled: color (one sample), sodium (three samples), sulfate (three samples), total dissolved solids (four samples), aluminum (one sample), arsenic (two samples), copper (one sample), iron (nine samples), manganese (eight samples), radon-222 (nine samples), and total coliform bacteria (six samples). Existing drinking-water standards for pH, chloride, fluoride, nitrate, nitrite, antimony, barium, beryllium, cadmium, chromium, lead, mercury, selenium, silver, thallium, zinc, gross alpha radioactivity, uranium, fecal coliform, Escherichia coli, and heterotrophic bacteria were not exceeded in any of the samples collected. None of the pesticides and VOCs analyzed exceeded existing drinking-water standards.

New York↗