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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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USGS2015

From submarine to lacustrine groundwater discharge

Submarine groundwater discharge (SGD) and its role in marine nutrient cycling are well known since the last decade. The freshwater equivalent, lacustrine groundwater discharge (LGD), is often still disregarded, although first reports of LGD are more than 50 years old. We identify nine different reasons why groundwater has long been disregarded in both freshwater and marine environments such as invisibility of groundwater discharge, the size of the interface and its difficult accessibility. Although there are some fundamental differences in the hydrology of SGD and LGD, caused primarily by seawater recirculation that occurs only in cases of SGD, there are also a lot of similarities such as a focusing of discharge to near-shore areas. Nutrient concentrations in groundwater near the groundwater–surface water interface might be anthropogenically enriched. Due to spatial heterogeneity of aquifer characteristics and biogeochemical processes, the quantification of groundwater-borne nutrient loads is challenging. Both nitrogen and phosphorus might be mobile in near-shore aquifers and in a lot of case studies large groundwater-borne nutrient loads have been reported.

Conference Paper↗

USGS2019

Differentiating anthropogenic and natural sources of uranium by geochemical fingerprinting of groundwater at the Homestake Uranium Mill, Milan, New Mexico, USA

A multiparameter geochemical-isotopic fingerprinting approach was used to differentiate natural and anthropogenic signatures of uranium contamination near the Homestake uranium mill site (Site), near Milan, New Mexico, USA. The Site consists of two tailings piles from milling operations and groundwater contamination from these tailings have been noted. The Site lies within the lower San Mateo Creek Basin with multiple regional sources of U contamination from mining and mill operations and is underlain by a heterogeneous alluvial aquifer, which is underlain by basement rock of the Chinle Group and the lowermost San Andres-Glorieta aquifer. To help decipher signatures, several statistical approaches were used including PCA, NMDS, and cluster analysis. Trilinear piper diagrams indicate two end member water types at the Site, sulfate-Na-K and sulfate-Ca. Natural alluvial aquifer groundwater in this area, relatively unaffected by mining or milling, appears to be more dominated by bicarbonate than sulfate and the deeper San Andres-Glorieta aquifer that has a mixture of sulfate and bicarbonate. Uranium concentrations from the Site fall into three broad categories, less than the drinking water standard of 30 µg/L (n=3), from 30 to 100 µg/L (n=9) and greater than 100 µg/L (n=8). Component loadings in a principal component analysis are highest for uranium isotopes, 228Ra, gross alpha-beta, molybdenum, chloride, uranium, and sodium, which affect the similarities or differences among wells sampled. Results suggest that several alluvial wells upgradient from the Site have anthropogenic fingerprints from regional sources related to upgradient mining. Wells with higher uranium concentrations have uranium activity ratios close to 1, which is indicative of mining or milling signatures. These same wells have elevated radon activities. This information can be used to inform Site managers on the source of water related to uranium at the Site and provide an approach for geochemical fingerprinting.

New Mexico↗

USGS1977

The age of groundwater in the Lincolnshire Limestone, England and its relevance to the flow mechanism

Groundwater samples from the Lincolnshire Limestone have been analysed for tritium, radiocarbon, and the stable-isotope ratios 13 C 12 C "> 13 C 12 C , 18 O 16 O "> 18 O 16 O and D/H. The age of the water increases in a downgradient direction below overlying confining deposits and reaches a maximum age greater than 25,000 years within 15 km of the outcrop. The δ 13 C ratio ultimately attains the unusually low negative values of −2‰ in a downgradient direction; this is approaching that of the aquifer matrix which is +2.35‰. The reason is believed to be exchange of carbon between the groundwater and the matrix by a continuous process of precipitation and further solution of calcium carbonate. The δ 18 O and δ D ratios imply that recharge of the aquifer during the late Pleistocene took place in the spring and autumn rather than the winter as at present. The data are interpreted by assuming that movement of water through the saturated zone is a combination of flow in fissures and “piston flow” through the micro-fissures and pores of the rock. The mechanism of water movement in the saturated zone is dominated by relatively rapid flow in fissures, but the fissure flow includes a contribution of much older water from “intergranular” storage which enters the fissures from the rock matrix by pressure differentials in the fissure distribution system and by diffusion. The distribution of water of different ages in the aquifer is closely related to recent groundwater abstraction patterns.

Journal of Hydrology↗

USGS1989

Effects of variations in recharge on groundwater quality

The predominant regional effect of recharge on municipal groundwater quality in Kansas is the dilution of mineralized water in aquifers with relatively shallow water tables. The individual dissolved constituents contributing most to the water-quality variations are sulfate and chloride, and the calcium and sodium accompanying them, which are derived from the dissolution of evaporite minerals within the aquifer or from saline formation water in bedrock underlying the aquifer. The relationship between recharge and groundwater-quality variation can be quantified by associating certain climatic indices, especially the Palmer Drought Index, with quality observations. The response time of the maximum water-quality change relative to the occurrence of drought or substantial recharge ranges from a month to 3 years depending on the aquifer characteristics, and is generally proportional to the saturated thickness and specific yield. The response time is also affected by discharge to and recharge from nearby streams and by the well construction, particularly the placement of the screened interval, and pumping stress.

Journal of Hydrology↗

USGS1993

Crude oil in a shallow sand and gravel aquifer-II. Organic geochemistry

Crude oil spilled from a pipeline break in a remote area of north-central Minnesota has contaminated a shallow glacial outwash aquifer. Part of the oil was sprayed over a large area to the west of the pipeline and part of it accumulated in an oil body that floats at the water table to the east of the point of discharge. Total dissolved organic carbon (TDOC) concentrations in shallow groundwater collected in the oil spray area reach 16 mg/l. This is nearly an order of magnitude higher than the TDOC concentrations of native groundwater (∼2–3mg/l). The additional TDOC derives from the partial degradation of petroleum residues deposited at the land surface and transported to the aquifer by vertical recharge. In the vicinity of the oil body, TDOC concentrations in groundwater are 48 mg/l, 58% of the TDOC being composed of non-volatile organic C. The majority of the volatile DOC (63%) is a mixture of low-molecular-weight saturated, aromatic and alicyclic hydrocarbons derived from the oil. Downgradient from the oil body along the direction of groundwater flow, concentrations of all measured constituents of the TDOC pool decrease. Concentrations begin to decline most rapidly, however, in the zone where dissolved O 2 concentrations begin to increase, ∼50m downgradient from the leading edge of the oil. Within the anoxic zone near the oil body, removal rates of isometric monoaromatic hydrocarbons vary widely. This indicates that the removal processes are mediated mainly by microbiological activity. Molecular and spectroscopic characterization of the TDOC and its spatial and temporal variation provide evidence of the importance of biogeochemical processes in attenuating petroleum contaminants in this perturbed subsurface environment.

Applied Geochemistry↗

USGS2016

Use of multiple age tracers to estimate groundwater residence times and long-term recharge rates in arid southern Oman

Multiple age tracers were measured to estimate groundwater residence times in the regional aquifer system underlying southwestern Oman. This area, known as the Najd, is one of the most arid areas in the world and is planned to be the main agricultural center of the Sultanate of Oman in the near future. The three isotopic age tracers 4 He, 14 C and 36 Cl were measured in waters collected from wells along a line that extended roughly from the Dhofar Mountains near the Arabian Sea northward 400 km into the Empty Quarter of the Arabian Peninsula. The wells sampled were mostly open to the Umm Er Radhuma confined aquifer, although, some were completed in the mostly unconfined Rus aquifer. The combined results from the three tracers indicate the age of the confined groundwater is < 40 ka in the recharge area in the Dhofar Mountains, > 100 ka in the central section north of the mountains, and up to and > one Ma in the Empty Quarter. The 14 C data were used to help calibrate the 4 He and 36 Cl data. Mixing models suggest that long open boreholes north of the mountains compromise 14 C-only interpretations there, in contrast to 4 He and 36 Cl calculations that are less sensitive to borehole mixing. Thus, only the latter two tracers from these more distant wells were considered reliable. In addition to the age tracers, δ 2 H and δ 18 O data suggest that seasonal monsoon and infrequent tropical cyclones are both substantial contributors to the recharge. The study highlights the advantages of using multiple chemical and isotopic data when estimating groundwater travel times and recharge rates, and differentiating recharge mechanisms.

Dhofar Mountains↗

USGS2019

Factors affecting the occurrence of lead and manganese in untreated drinking water from Atlantic and Gulf Coastal Plain aquifers, eastern United States—Dissolved oxygen and pH framework for evaluating risk of elevated concentrations

Groundwater samples collected during 2012 and 2013 from public-supply wells screened in the Atlantic and Gulf Coastal Plain aquifers of the eastern and southeastern U.S. rarely contained lead or manganese concentrations that exceeded drinking-water limits, despite having corrosive characteristics. Data indicate that the occurrence of dissolved lead and manganese in sampled groundwater, prior to its distribution or treatment, was related to several explanatory factors including the presence of source minerals, hydrologic position along the flow path, water-rock interactions, and associated geochemical conditions such as pH and dissolved oxygen (DO) concentrations. Elevated concentrations of lead compared to health-based benchmarks were associated with groundwater that is acidic (pH ≤ 6.5), oxygenated (DO ≥ 2 mg/L), and closer to recharge zones (relatively young water). Elevated concentrations of manganese were associated with groundwater that is acidic to neutral (pH ≤ 7.5), has low DO (<2 mg/L), and further from recharge zones (relatively old). Under these geochemical conditions, minerals that could sequester lead or manganese tended to be undersaturated, and adsorption by hydrous ferric oxide was limited. Under neutral to alkaline pH conditions, precipitation of impure calcium carbonate or phosphate compounds containing traces of lead or manganese (solid solutions) could maintain low concentrations of the trace elements. Additionally, adsorption of lead or manganese cations by hydrous ferric oxides (HFO) could be another attenuating factor where conditions are oxidizing and dissolved inorganic carbon concentrations are relatively low. A DO/pH framework was developed as a screening tool for evaluating risk of elevated lead or manganese, based on the occurrence of elevated lead and manganese concentrations and the corresponding distributions of DO and pH in the Atlantic and Gulf Coastal Plain aquifers. Validation of the DO/pH framework was accomplished using an independent national dataset that showed consistent results for elevated lead (pH ≤ 6.5; DO ≥ 2 mg/L) and manganese (pH ≤ 7.5; DO < 2 mg/L).

Atlantic and Gulf Coastal Plain aquifers↗

USGS2021

Noble gas signatures constrain oil-field water as the carrier phase of hydrocarbons occurring in shallow aquifers in the San Joaquin Basin, USA

Noble gases record fluid interactions in multiphase subsurface environments through fractionation processes during fluid equilibration. Water in the presence of hydrocarbons at the subsurface acquires a distinct elemental signature due to the difference in solubility between these two fluids. We find the atmospheric noble gas signature in produced water is partially preserved after hydrocarbons production and water disposal to unlined ponds at the surface. This signature is distinct from meteoric water and can be used to trace oil-field water seepage into groundwater aquifers. We analyse groundwater ( n = 30) and fluid disposal pond ( n = 2) samples from areas overlying or adjacent to the Fruitvale, Lost Hills, and South Belridge Oil Fields in the San Joaquin Basin, California, USA. Methane (2.8 × 10 −7 to 3 × 10 −2 cm 3 STP/cm 3 ) was detected in 27 of 30 groundwater samples. Using atmospheric noble gas signatures, the presence of oil-field water was identified in 3 samples, which had equilibrated with thermogenic hydrocarbons in the reservoir. Two (of the three) samples also had a shallow microbial methane component, acquired when produced water was deposited in a disposal pond at the surface. An additional 6 samples contained benzene and toluene, indicative of interaction with oil-field water; however, the noble gas signatures of these samples are not anomalous. Based on low tritium and 14 C contents (≤ 0.3 TU and 0.87–6.9 pcm, respectively), the source of oil-field water is likely deep, which could include both anthropogenic and natural processes. Incorporating noble gas analytical techniques into the groundwater monitoring programme allows us to 1) differentiate between thermogenic and microbial hydrocarbon gas sources in instances when methane isotope data are unavailable, 2) identify the carrier phase of oil-field constituents in the aquifer (gas, oil-field water, or a combination), and 3) differentiate between leakage from a surface source (disposal ponds) and from the hydrocarbon reservoir (either along natural or anthropogenic pathways such as faulty wells).

California↗

USGS2021

Manganese in the Northern Atlantic Coastal Plain aquifer system, eastern USA—Modeling regional occurrence with pH, redox, and machine learning

Study region : The study was conducted in the Northern Atlantic Coastal Plain aquifer system, eastern USA, an important water supply in a densely populated region. Study focus : Manganese (Mn), an emerging health concern and common nuisance contaminant in drinking water, is mapped and modeled using the XGBoost machine learning method, predictions of pH and redox conditions from previous models, and other explanatory variables that describe the groundwater flow system and surface characteristics. Methods to address the imbalanced occurrence of elevated and low Mn concentrations are compared and used to more accurately predict concentrations of interest for human health and drinking water quality. New hydrological insights for the region : Elevated Mn concentrations were more likely in shallow groundwater, close to recharge areas and in topographically low areas where soil or unsaturated processes influence groundwater quality. Predicted concentrations greater than the health threshold of 300 micrograms per liter extended across 17 % of the surficial aquifer area, but across <1% of the areas of underlying aquifers. pH and variables related to flow-system position and near-surface processes were more important predictors than the probability of low dissolved oxygen (DO). Mapped variable influence (SHAP values) showed that both pH and DO variables were related to hydrogeologic conditions. Class weights, which improved the predictive ability for elevated Mn without altering the data, was the preferred method to address class imbalance.

Maryland, New Jersey, New York, North Carolina, Pe↗

USGS2008

Distribution and variability of redox zones controlling spatial variability of arsenic in the Mississippi River Valley alluvial aquifer, southeastern Arkansas

Twenty one of 118 irrigation water wells in the shallow (25-30??m thick) Mississippi River Valley alluvial aquifer in the Bayou Bartholomew watershed, southeastern Arkansas had arsenic (As) concentrations (< 0.5 to 77????g/L) exceeding 10????g/L. Sediment and groundwater samples were collected and analyzed from the sites of the highest, median, and lowest concentrations of As in groundwater in the alluvial aquifers located at Jefferson County, Arkansas. A traditional five-step sequential extraction was performed to differentiate the exchangeable, carbonate, amorphous Fe and Mn oxide, organic, and hot HNO3-leachable fraction of As and other compounds in sediments. The Chao reagent (0.25??M hydroxylamine hydrochloride in 0.25??M HCl) removes amorphous Fe and Mn oxides and oxyhydroxides (present as coatings on grains and amorphous minerals) by reductive dissolution and is a measure of reducible Fe and Mn in sediments. The hot HNO3 extraction removes mostly crystalline metal oxides and all other labile forms of As. Significant total As (20%) is complexed with amorphous Fe and Mn oxides in sediments. Arsenic abundance is not significant in carbonates or organic matter. Significant (40-70????g/kg) exchangeable As is only present at shallow depth (0-1??m below ground surface). Arsenic is positively correlated to Fe extracted by Chao reagent (r = 0.83) and hot HNO3 (r = 0.85). Arsenic extracted by Chao reagent decreases significantly with depth as compared to As extracted by hot HNO3. Fe (II)/Fe (the ratio of Fe concentration in the extracts of Chao reagent and hot HNO3) is positively correlated (r = 0.76) to As extracted from Chao reagent. Although Fe (II)/Fe increases with depth, the relative abundance of reducible Fe decreases noticeably with depth. The amount of reducible Fe, as well as As complexed to amorphous Fe and Mn oxides and oxyhydroxides decreases with depth. Possible explanations for the decrease in reducible Fe and its complexed As with depth include historic flushing of As and Fe from hydrous ferric oxides (HFO) by microbially-mediated reductive dissolution and aging of HFO to crystalline phases. Hydrogeochemical data suggests that the groundwater in the area falls in the mildly reducing (suboxic) to relatively highly reducing (anoxic) zone, and points to reductive dissolution of HFO as the dominant As release mechanism. Spatial variability of gypsum solubility and simultaneous SO42- reduction with co-precipitation of As and sulfide is an important limiting process controlling the concentration of As in groundwater in the area. ?? 2008 Elsevier B.V. All rights reserved.

Journal of Contaminant Hydrology↗

USGS2023

Photochemical mobilization of dissolved hydrocarbon oxidation products from petroleum contaminated soil into a shallow aquifer activate human nuclear receptors

Elevated non-volatile dissolved organic carbon (NVDOC) concentrations in groundwater monitoring wells under oil-contaminated hydrophobic soils originating from a pipeline rupture at the National Crude Oil Spill & Natural Attenuation Research Site near Bemidji, MN are documented.. We hypothesized the elevated NVDOC is comprised of water-soluble photooxidation products transported from the surface to the aquifer. We use field and laboratory samples in combination with complementary analytical methods to test this hypothesis and determine the biological response to these products. Observations from optical spectroscopy and ultrahigh-resolution mass spectrometry reveal a significant correlation between the chemical composition of NVDOC leached from photochemically weathered soils and groundwater monitoring wells with high NVDOC concentrations measured in the aquifer beneath the contaminated soil. Conversely, the chemical composition from the uncontaminated soil photoleachate, matches the NVDOC observed in the uncontaminated wells. Contaminated groundwater and photodissolution leachates from contaminated soil activated biological targets indicative of xenobiotic metabolism and exhibited potential for adverse effects. Newly formed hydrocarbon oxidation products (HOPs) from fresh oil could be distinguished from those downgradient. This study illustrates another pathway for dissolved HOPs to infiltrate groundwater and potentially affect human health and the environment.

Minnesota↗

USGS2021

Prevalence of neonicotinoids and sulfoxaflor in alluvial aquifers in a high corn and soybean producing region of the Midwestern United States

Neonicotinoids have been previously detected in Iowa surface waters, but less is known regarding their occurrence in groundwater. To help fill this research gap, a groundwater study was conducted in eastern Iowa and southeastern Minnesota, a corn and soybean producing area with known heavy neonicotinoid use. Neonicotinoids were studied in alluvial aquifers, a hydrogeologic setting known to be vulnerable to surface-applied contaminants. Groundwater samples were analyzed from 40 wells for six neonicotinoid compounds (acetamiprid, clothianidin , dinotefuran, imidacloprid, thiacloprid, thiamethoxam), and sulfoxaflor. Samples were analyzed using liquid chromatography tandem mass spectrometry (LC/MS/MS) with both direct aqueous injection and solid phase extraction methods. Neonicotinoids were prevalent in the alluvial aquifers with 73% of the wells having at least one neonicotinoid detection. Clothianidin (68%, max: 391.7 ng/L) was the most commonly detected, followed by imidacloprid (43%, max: 6.7 ng/L) and thiamethoxam (3%, max: 0.2 ng/L). Acetamiprid, dinotefuran, sulfoxaflor, and thiacloprid were not detected during the study. The solid phase extraction method was more sensitive than direct aqueous injection, where only clothianidin detected in 23% of samples. SPE is the preferred method for detecting low concentrations of hydrophilic pesticides in water. This study documented that the combination of heavy chemical use overlying a hydrogeologic setting vulnerable to surface applied contaminants leads to transport of neonicotinoids into an important groundwater resource.

Iowa↗

USGS1999

Evaluation of confidence intervals for a steady-state leaky aquifer model

The fact that dependent variables of groundwater models are generally nonlinear functions of model parameters is shown to be a potentially significant factor in calculating accurate confidence intervals for both model parameters and functions of the parameters, such as the values of dependent variables calculated by the model. The Lagrangian method of Vecchia and Cooley [Vecchia, A.V. and Cooley, R.L., Water Resources Research, 1987, 23(7), 1237-1250] was used to calculate nonlinear Scheffe-type confidence intervals for the parameters and the simulated heads of a steady-state groundwater flow model covering 450 km2 of a leaky aquifer. The nonlinear confidence intervals are compared to corresponding linear intervals. As suggested by the significant nonlinearity of the regression model, linear confidence intervals are often not accurate. The commonly made assumption that widths of linear confidence intervals always underestimate the actual (nonlinear) widths was not correct. Results show that nonlinear effects can cause the nonlinear intervals to be asymmetric and either larger or smaller than the linear approximations. Prior information on transmissivities helps reduce the size of the confidence intervals, with the most notable effects occurring for the parameters on which there is prior information and for head values in parameter zones for which there is prior information on the parameters.The fact that dependent variables of groundwater models are generally nonlinear functions of model parameters is shown to be a potentially significant factor in calculating accurate confidence intervals for both model parameters and functions of the parameters, such as the values of dependent variables calculated by the model. The Lagrangian method of Vecchia and Cooley was used to calculate nonlinear Scheffe-type confidence intervals for the parameters and the simulated heads of a steady-state groundwater flow model covering 450 km2 of a leaky aquifer. The nonlinear confidence intervals are compared to corresponding linear intervals. As suggested by the significant nonlinearity of the regression model, linear confidence intervals are often not accurate. The commonly made assumption that widths of linear confidence intervals always underestimate the actual (nonlinear) widths was not correct. Results show that nonlinear effects can cause the nonlinear intervals to be asymmetric and either larger or smaller than the linear approximations. Prior information on transmissivities helps reduce the size of the confidence intervals, with the most notable effects occurring for the parameters on which there is prior information and for head values in parameter zones for which there is prior information on the parameters.

Advances in Water Resources↗

USGS2012

Can arsenic occurrence rate in bedrock aquifers be predicted?

A high percentage (31%) of groundwater samples from bedrock aquifers in the greater Augusta area, Maine was found to contain greater than 10 μg L –1 of arsenic. Elevated arsenic concentrations are associated with bedrock geology, and more frequently observed in samples with high pH, low dissolved oxygen, and low nitrate. These associations were quantitatively compared by statistical analysis. Stepwise logistic regression models using bedrock geology and/or water chemistry parameters are developed and tested with external data sets to explore the feasibility of predicting groundwater arsenic occurrence rates (the percentages of arsenic concentrations higher than 10 μg L –1 ) in bedrock aquifers. Despite the under-prediction of high arsenic occurrence rates, models including groundwater geochemistry parameters predict arsenic occurrence rates better than those with bedrock geology only. Such simple models with very few parameters can be applied to obtain a preliminary arsenic risk assessment in bedrock aquifers at local to intermediate scales at other localities with similar geology.

Environmental Science & Technology↗

USGS2012

GeoChip-based analysis of microbial functional gene diversity in a landfill leachate-contaminated aquifer

The functional gene diversity and structure of microbial communities in a shallow landfill leachate-contaminated aquifer were assessed using a comprehensive functional gene array (GeoChip 3.0). Water samples were obtained from eight wells at the same aquifer depth immediately below a municipal landfill or along the predominant downgradient groundwater flowpath. Functional gene richness and diversity immediately below the landfill and the closest well were considerably lower than those in downgradient wells. Mantel tests and canonical correspondence analysis (CCA) suggested that various geochemical parameters had a significant impact on the subsurface microbial community structure. That is, leachate from the unlined landfill impacted the diversity, composition, structure, and functional potential of groundwater microbial communities as a function of groundwater pH, and concentrations of sulfate, ammonia, and dissolved organic carbon (DOC). Historical geochemical records indicate that all sampled wells chronically received leachate, and the increase in microbial diversity as a function of distance from the landfill is consistent with mitigation of the impact of leachate on the groundwater system by natural attenuation mechanisms.

Oklahoma↗

USGS2021

Assessing the feasibility of managed aquifer recharge in California

With aquifers around the world stressed by over-extraction, water managers are increasingly turning to managed aquifer recharge (MAR), directly replenishing groundwater resources through injection wells, recharge basins, or other approaches. While there has been progress in understanding the geological and infrastructure-related considerations to make MAR more effective, critical evaluations of its institutional design and implementation are limited. This study assesses MAR projects, using a case study of projects proposed by groundwater sustainability agencies (GSAs) in California to comply with the state's Sustainable Groundwater Management Act of 2014; these projects will almost double the number of MAR projects in the United States. We draw on content analysis of groundwater sustainability plans that propose these projects. We first assess the types of recharge projects proposed and the stated aims of the projects, to assess when and why agencies are turning to MAR as a solution. We find that recharge basins are by far the most common approach, and that GSAs hope these basins will improve water table levels, reduce subsidence, and improve water quality. We then analyze potential barriers to project implementation and assess the projects' ability to achieve the stated goals. Primary concerns identified include a potential lack of available water, a potentially challenging legal framework, and minimal consideration of funding and cumulative land needs. To conclude, we discuss broader considerations for ensuring that MAR is an effective water management tool.

California↗

USGS2010

Deducing the distribution of terminal electron-accepting processes in hydrologically diverse groundwater systems

The distribution of microbially mediated terminal electron-accepting processes (TEAPs( was investigated in four hydrologically diverse groundwater systems by considering patterns of electron acceptor (nitrate, sulfate) consumption, intermediate product (hydrogen (H 2 )) concentrations, and final product (ferrous iron, sulfide, and methane) production. In each hydrologic system a determination of predominant TEAPs could be arrived at, but the level of confidence appropriate for each determination differed. In a portion of the lacustrine aquifer of the San Joaquin Valley, for example, all three indicators (sulfate concentrations decreasing, H 2 concentrations in the 1–2 nmol range, and sulfide concentrations increasing along flow paths identified sulfate reduction as the predominant TEAP, leading to a high degree of confidence in the determination. In portions of the Floridan aquifer and a petroleum hydrocarbon-contaminated aquifer, sulfate reduction and methanogenesis are indicated by production of sulfide and methane, and hydrogen oncentrations in the 1–4 nmol and 5–14 nmol range, respectively. However, because electron acceptor consumption could not be documented in these systems, less confidence is warranted in the TEAP determination. In the Black Creek aquifer, no pattern of sulfate consumption and sulfide production were observed, but H2 concentrations indicated sulfate reduction as the predominant TEAP. In this case, where just a single line of evidence is available, the least confidence in the TEAP diagnosis is justified. Because this methodology is based on measurable water chemistry parameters and upon the physiology of microbial electron transfer processes, it provides a better description of predominant redox processes in groundwater systems than more traditional Eh-based methods.

Water Resources Research↗

USGS1998

Detection of aquifer system compaction and land subsidence using interferometric synthetic aperture radar, Antelope Valley, Mojave Desert, California

Interferometric synthetic aperture radar (InSAR) has great potential to detect and quantify land subsidence caused by aquifer system compaction. InSAR maps with high spatial detail and resolution of range displacement (±10 mm in change of land surface elevation) were developed for a groundwater basin (∼10 3 km 2 ) in Antelope Valley, California, using radar data collected from the ERS-1 satellite. These data allow comprehensive comparison between recent (1993–1995) subsidence patterns and those detected historically (1926–1992) by more traditional methods. The changed subsidence patterns are generally compatible with recent shifts in land and water use. The InSAR-detected patterns are generally consistent with predictions based on a coupled model of groundwater flow and aquifer system compaction. The minor inconsistencies may reflect our imperfect knowledge of the distribution and properties of compressible sediments. When used in conjunction with coincident measurements of groundwater levels and other geologic information, InSAR data may be useful for constraining parameter estimates in simulations of aquifer system compaction.

California↗