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At least 487 records · Page 27Linked to original sources
USGS2023

Analysis of aquifer framework and properties, North Magee Street well field, Southampton, New York

The U.S. Geological Survey, in cooperation with the Suffolk County Water Authority, evaluated the groundwater-flow characteristics and aquifer properties of the North Magee Street well field north of the village of Southampton, New York. Characteristics and properties included groundwater-flow direction, potential groundwater-contributing areas to the well field production wells, and aquifer transmissivity and storage. The groundwater flow and aquifer properties were also evaluated to allow Suffolk County Water Authority to better assess the potential source of dissolved halocarbons (refrigerants, such as chlorofluorocarbons). The well field production wells are screened in the upper glacial aquifer and an observation well is screened in the Magothy aquifer. Based on depth and available logs, groundwater from wells screened in the upper glacial aquifer was classified as under water-table (unconfined) conditions, and groundwater from wells screened in the Magothy aquifer was classified as being under semiconfined conditions. Groundwater flows radially to the well field during production and in a northwesterly direction under the effect of the regional flow regime. A previously published particle tracking analysis identified the following recharge contributing areas nearby the well field: (1) contributing areas to surface-water bodies of the Peconic Estuary, (2) contributing areas to surface-water bodies of the South Shore Estuary Reserve, (3) a contributing area to the Atlantic Ocean, and (4) a contributing area to another Suffolk County Water Authority well field. Five other pumping well contributing areas were identified within the study area, including those of various wells pumped for golf-course irrigation. Analysis of drawdown and recovery data collected during the multiple-well aquifer test, through the application of a Neuman analytical model, provided estimates of upper glacial aquifer characteristics and properties. Inclusion of lateral aquifer boundaries was not necessary for the analysis to result in satisfactory matches with the observed water-level responses. Aquifer transmissivity was estimated to be 170,000 feet squared per day. Storativity was estimated to be 0.02 (dimensionless), and specific yield was estimated to be 0.08 (dimensionless), consistent with the inferred degree of confinement and well field characteristics.

New York↗
USGS1987

Ground-water conditions in Avra Valley, Pima and Pinal Counties, Arizona -1985

Avra Valley is a north-trending alluvial basin about 15 mi west of Tucson in Pima and Pinal Counties in south-central Arizona. The valley includes about 520 sq mi of which about 100 sq mi is in the San Xavier Indian Reservation. The basin is bounded on the east by the Tortolita, Tucson, and Sierrita Mountains and on the west by the Picacho, Silverbell, and Roskruge Mountains. The climate of the valley is semiarid, the average annual precipitation ranges from 8 to 12 in., and the average annual lake evaporation ranges from 58 to 62 in. Two major ephemeral streams--Santa Cruz River and Brawley Wash--drain the area. Santa Cruz River and Brawley Wash and their tributaries provide a source of recharge to an extensive alluvial aquifer that underlies the valley floor. Since 1940, the amount of groundwater pumped from the aquifer has been greater than the amount of natural recharge from infiltration and underflow. Overdraft of the aquifer resulted in substantial water level declines throughout the valley. Until 1969, use of groundwater in Avra Valley was for irrigation. Since 1969, the city of Tucson has pumped and transported groundwater for municipal use in the adjacent Tucson basin from lands that were purchased and retired from agriculture. The purpose of this report is to describe groundwater conditions in Avra Valley as of 1985. A brief discussion of the geohydrologic setting and history of groundwater development are given to define aquifer characteristics, changes in groundwater levels, and groundwater pumpage since 1940. (Lantz-PTT)

Arizona↗
USGS2002

Using chemical, hydrologic, and age dating analysis to delineate redox processes and flow paths in the riparian zone of a glacial outwash aquifer‐stream system

A combination of chemical and dissolved gas analyses, chlorofluorocarbon age dating, and hydrologic measurements were used to determine the degree to which biogeochemical processes in a riparian wetland were responsible for removing NO 3 − from groundwaters discharging to the Otter Tail River in west central Minnesota. An analysis of river chemistry and flow data revealed that NO 3 − concentrations in the river increased in the lower half of the 8.3 km study reach as the result of groundwater discharge to the river. Groundwater head measurements along a study transect through the riparian wetland revealed a zone of groundwater discharge extending out under the river. On the basis of combined chemical, dissolved gas, age date, and hydrologic results, it was determined that water chemistry under the riparian wetland was controlled largely by upgradient groundwaters that followed flow paths up to 16 m deep and discharged under the wetland, creating a pattern of progressively older, more chemically reduced, low NO 3 − water the farther one progressed from the edge of the wetland toward the river. These findings pose challenges for researchers investigating biogeochemical processes in riparian buffer zones because the progressively older groundwaters entered the aquifer in earlier years when less NO 3 − fertilizer was being used. NO 3 − concentrations originally present in the groundwater had also decreased in the upgradient aquifer as a result of denitrification and progressively stronger reducing conditions there. The resulting pattern of decreasing NO 3 − concentrations across the riparian zone may be incorrectly interpreted as evidence of denitrification losses there instead of in the upgradient aquifer. Consequently, it is important to understand the hydrogeologic setting and age structure of the groundwaters being sampled in order to avoid misinterpreting biogeochemical processes in riparian zones.

Water Resources Research↗
USGS2017

Groundwater model of the Great Basin carbonate and alluvial aquifer system version 3.0: Incorporating revisions in southwestern Utah and east central Nevada

The groundwater model described in this report is a new version of previously published steady-state numerical groundwater flow models of the Great Basin carbonate and alluvial aquifer system, and was developed in conjunction with U.S. Geological Survey studies in Parowan, Pine, and Wah Wah Valleys, Utah. This version of the model is GBCAAS v. 3.0 and supersedes previous versions. The objectives of the model for Parowan Valley were to simulate revised conceptual estimates of recharge and discharge, to estimate simulated aquifer storage properties and the amount of reduction in storage as a result of historical groundwater withdrawals, and to assess reduction in groundwater withdrawals necessary to mitigate groundwater-level declines in the basin. The objectives of the model for the area near Pine and Wah Wah Valleys were to recalibrate the model using new observations of groundwater levels and evapotranspiration of groundwater; to provide new estimates of simulated recharge, hydraulic conductivity, and interbasin flow; and to simulate the effects of proposed groundwater withdrawals on the regional flow system. Meeting these objectives required the addition of 15 transient calibration stress periods and 14 projection stress periods, aquifer storage properties, historical withdrawals in Parowan Valley, and observations of water-level changes in Parowan Valley. Recharge in Parowan Valley and withdrawal from wells in Parowan Valley and two nearby wells in Cedar City Valley vary for each calibration stress period representing conditions from March 1940 to November 2013. Stresses, including recharge, are the same in each stress period as in the steady-state stress period for all areas outside of Parowan Valley. The model was calibrated to transient conditions only in Parowan Valley. Simulated storage properties outside of Parowan Valley were set the same as the Parowan Valley properties and are not considered calibrated. Model observations in GBCAAS v. 3.0 are groundwater levels at wells and discharge locations; water-level changes; and discharge to springs, evapotranspiration of groundwater, rivers, and lakes. All observations in the model outside of Parowan Valley are considered to represent steady-state conditions. Composite scaled sensitivities indicate the observations of discharge to rivers and springs provide more information about model parameters in the model focus area than do water-level observations. Water levels and water-level changes, however, provide the only information about specific yield and specific storage parameters and provide more information about recharge and withdrawals in Parowan Valley than any other observation group. Comparisons of simulated water levels and measured water levels in Parowan Valley indicated that the model fits the overall trend of declining water levels and provides reasonable estimates of long-term reduction in storage and of storage changes from 2012 to 2013. The conceptual and simulated groundwater budgets for Parowan Valley from November 2012 to November 2013 are similar, with recharge of about 20,000 acre-feet and discharge of about 45,000 acre-feet. In the simulation, historical withdrawals averaging about 28,000 acre-feet per year (acre-ft/yr) cause major changes in the groundwater system in Parowan Valley. These changes include the cessation of almost all natural discharge in the valley and the long-term removal of water from storage. Simulated recharge in Pine Valley of 11,000 acre-ft/yr and in Wah Wah Valley of 3,200 acre-ft/yr is substantially less in GBCAAS v. 3.0 than that simulated by previous model versions. In addition, the valleys have less simulated inflow from and outflow to other hydrographic areas than were simulated by previous model versions. The effects of groundwater development in these valleys, however, are independent of the amount of water recharging in and flowing through the valleys. Groundwater withdrawals in Pine and Wah Wah Valleys will decrease groundwater storage (causing drawdown) until discharge in surrounding areas and mountain springs around the two valleys is reduced by the rate of withdrawal. The model was used to estimate that reducing withdrawals in Parowan Valley from 35,000 to about 22,000 acre-ft/yr would likely stabilize groundwater levels in the valley if recharge varies as it did from about 1950 to 2012. The model was also used to demonstrate that withdrawals of 15,000 acre-ft/yr from Pine Valley and 6,500 acre-ft/yr from Wah Wah Valley could ultimately cause long-term steady-state water-level declines of about 1,900 feet near the withdrawal wells and of more than 5 feet in an area of about 10,500 square miles. The timing of drawdown and capture and the ultimate amount of drawdown are dependent on the proximity to areas of simulated natural groundwater discharge, simulated transmissivity, and simulated storage properties. The model projections are a representation of possible effects.

Nevada, Utah↗
USGS2016

Status of groundwater levels and storage volume in the Equus Beds aquifer near Wichita, Kansas, January 2016

The Equus Beds aquifer in south-central Kansas, which is part of the High Plains aquifer, serves as a source of water for municipal and agricultural users in the area. The city of Wichita has used the Equus Beds aquifer as one of its primary water sources since the 1940s. The aquifer in and around Wichita’s well field reached historically low water levels in 1993, prompting the city to adopt new water-use and conservation strategies to ensure future water supply needs were met. Part of the plan was to initiate a managed aquifer recharge program called the Equus Beds Aquifer Storage and Recovery project. The goal of the managed aquifer recharge program is to artificially recharge the Equus Beds aquifer with treated water from the Little Arkansas River. As part of the Equus Beds Aquifer Storage and Recovery project, the city of Wichita and the U.S. Geological Survey have partnered in a long-term cooperative study to monitor and describe the quantity and quality of the water in the Equus Beds aquifer and the Little Arkansas River. The city of Wichita, the Equus Beds Groundwater Management District No. 2, the Kansas Department of Agriculture–Division of Water Resources, and the U.S. Geological Survey collected groundwater levels in numerous wells screened in the Equus Beds aquifer in the area in and around Wichita’s well field in January 2016. The measurements were used to interpolate potentiometric surfaces for shallow and deep parts of the aquifer in the study area. These potentiometric surfaces were compared with potentiometric surfaces from previous years to estimate changes in water levels and storage volume in the study area. Groundwater levels were generally higher in January 2016 than they were in January 2015. On average, in January 2016, groundwater levels in the shallow part of the aquifer were about 3.4 feet higher and groundwater levels in the deep part of the aquifer were about 3.8 feet higher than in January 2015. The volume of water stored in the study area decreased by about 74,000 acre-feet between predevelopment (the time period before substantial pumpage began in the 1940s) and January 2016; increased by about 121,000 acre-feet between the historic low in 1993 and January 2016; and increased by about 61,000 acre-feet between January 2015 and January 2016. About 62 percent of the storage volume lost between predevelopment and 1993 has been recovered. The increase in storage volume from January 2015 to January 2016 can probably be attributed to less pumping by the city of Wichita and irrigators, more recharge due to higher-than-average precipitation, and higher volumes of artificial recharge in 2015.

Kansas↗
USGS2014

The quality of our Nation's waters: Water quality in the Denver Basin aquifer system, Colorado, 2003-05

Availability and sustainability of groundwater in the Denver Basin aquifer system depend on water quantity and water quality. The Denver Basin aquifer system underlies about 7,000 square miles of the Great Plains in eastern Colorado and is the primary or sole source of water for domestic and public supply in many areas of the basin. Use of groundwater from the Denver Basin sandstone aquifers has been instrumental for development of the south Denver metropolitan area and other areas, but has resulted in a decline in water levels in some parts of the system. Human activities in many areas have adversely affected the quality of water in the aquifer system, especially the shallow parts. Groundwater in deeper parts of the system used for drinking water, once considered isolated from the effects of overlying land use, is increasingly vulnerable to contamination from human activities and geologic materials. Availability and sustainability of high-quality groundwater are vital to the economic health of the Denver Basin area.

Colorado↗
USGS2012

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

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

California↗
USGS1996

Preliminary assessment of the occurrence and possible sources of MTBE in groundwater in the United States, 1993-1994

The 1990 Clean Air Act Amendments require fuel oxygenates to be added to gasoline used in some metropolitan areas to reduce atmospheric concentrations of carbon monoxide or ozone. Methyl tert-butyl ether (MTBE) is the most commonly used fuel oxygenate and is a relatively new gasoline additive. Nevertheless, out of 60 volatile organic chemicals analyzed, MTBE was the second most frequently detected chemical in samples of shallow ambient groundwater from urban areas that were collected during 1993-1994 aspart of the U.S. Geological Survey's National Water-Quality Assessment program. Samples were collected from five drinking water wells, 12 springs, and 193 monitoring wells in urban areas. No MTBE was detected in drinking water wells. At a reporting level of 0.2 ??g/L, MTBE was detected most frequently in shallow groundwater from urban areas (27% of 210 wells and springs sampled in eight areas) as compared to shallow groundwater from agricultural areas (1.3% of 549 wells sampled in 21 areas) or deeper groundwater from major aquifers (1.0% of 412 wells sampled in nine areas). Only 3% of the shallow wells sampled in urban areas had concentrations of MTBE that exceed 20 ??g/L, which is the estimated lower limit of the United States Environmental Protection Agency draft drinking water health advisory. Because MTBE is persistent and mobile in groundwater, it can move from shallow to deeper aquifers with time. In shallow urban groundwater, MTBE generally was not found with benzene, toluene, ethylbenzene, or xylene (BTEX) compounds, which commonly are associated with gasoline spills. This disassociation causes uncertainty as to the source of MTBE. Possible sources of MTBE in groundwater include point sources, such as leaking storage tanks, and non-point sources, such as recharge of precipitation and stormwater runoff.

Environmental Science & Technology↗
USGS2009

Elevated naturally occurring arsenic in a semiarid oxidizing system, Southern High Plains aquifer, Texas, USA

High groundwater As concentrations in oxidizing systems are generally associated with As adsorption onto hydrous metal (Al, Fe or Mn) oxides and mobilization with increased pH. The objective of this study was to evaluate the distribution, sources and mobilization mechanisms of As in the Southern High Plains (SHP) aquifer, Texas, relative to those in other semiarid, oxidizing systems. Elevated groundwater As levels are widespread in the southern part of the SHP (SHP-S) aquifer, with 47% of wells exceeding the current EPA maximum contaminant level (MCL) of 10 μg/L (range 0.3–164 μg/L), whereas As levels are much lower in the north (SHP-N: 9% ⩾ As MCL of 10 μg/L; range 0.2–43 μg/L). The sharp contrast in As levels between the north and south coincides with a change in total dissolved solids (TDS) from 395 mg/L (median north) to 885 mg/L (median south). Arsenic is present as arsenate (As V) in this oxidizing system and is correlated with groundwater TDS (Spearman’s ρ = 0.57). The most likely current source of As is sorbed As onto hydrous metal oxides based on correlations between As and other oxyanion-forming elements (V, ρ = 0.88; Se, ρ = 0.54; B, ρ = 0.51 and Mo, ρ = 0.46). This source is similar to that in other oxidizing systems and constitutes a secondary source; the most likely primary source being volcanic ashes in the SHP aquifer or original source rocks in the Rockies, based on co-occurrence of As and F ( ρ = 0.56), oxyanion-forming elements and SiO 2 ( ρ = 0.41), which are found in volcanic ashes. High groundwater As concentrations in some semiarid oxidizing systems are related to high evaporation. Although correlation of As with TDS in the SHP aquifer may suggest evaporative concentration, unenriched stable isotopes (δ 2 H: −65 to −27; δ 18 O: −9.1 to −4.2) in the SHP aquifer do not support evaporation. High TDS in the SHP aquifer is most likely related to upward movement of saline water from the underlying Triassic Dockum aquifer. Mobilization of As in other semiarid oxidizing systems is caused by increased pH; however, pH in the SHP aquifer is near neutral (10–90 percentiles, 7.0–7.6). Although many processes, such as competitive desorption with SiO 2 , VO 4 , or PO 4 , could be responsible for local mobilization of As in the SHP aquifer, the most plausible explanation for the regional As distribution and correlation with TDS is the counterion effect caused by a change from Ca- to Na-rich, water as shown by the high correlation between As and Na/(Ca) 0.5 ratios ( ρ = 0.57). This change in chemistry is related to mixing with saline water that moves upward from the underlying Dockum aquifer. This counterion effect may mobilize other anions and oxyanion-forming elements that are correlated with As (F, V, Se, B, Mo and SiO 2 ). Competition among the oxyanions for sorption sites may enhance As mobilization. The SHP case study has similar As sources to those of other semiarid, oxidizing systems (original volcanic ash source followed by sorption onto hydrous metal oxides) but contrasts with these systems by showing lack of evaporative concentration and pH mobilization of As but counterion mobilization of As instead in the SHP-S aquifer.

Texas↗
USGS1997

Preliminary assessment of the occurrence and possible sources of MTBE in groundwater in the United States, 1993-1994

The 1990 Clean Air Act Amendments require fuel oxygenates to be added to gasoline used in some metropolitan areas to reduce atmospheric concentrations of carbon monoxide or ozone. Methyl tert-butyl ether (MTBE), is the most commonly used fuel oxygenate and is a relatively new gasoline additive. Nevertheless, out of 60 volatile organic chemicals analyzed, MTBE was the second most frequently detected chemical in samples of shallow ambient groundwater from urban areas that were collected during 1993-94 as part of the U.S. Geological Survey's National Water-Quality Assessment Program. Samples were collected from 5 drinking-water wells, 12 springs, and 1g3 monitoring wells in urban areas. No MTBE was detected in drinking-water wells. At a reporting level of 0.2 ??g/L, MTBE was detected most frequently in shallow groundwater from urban areas (27% of 210 wells and springs sampled in 8 areas) as compared to shallow groundwater from agricultural areas (1.3% of 549 wells sampled in 21 areas) or deeper groundwater from major aquifers (1.0% of 412 wells sampled in 9 areas). Only 3% of the shallow wells sampled in urban areas had concentrations of MTBE that exceed 20 ??g/L, which is the estimated lower limit of the United States Environmental Protection Agency draft lifetime drinking water health advisory. Because MTBE is persistent and mobile in groundwater) it can move from shallow to deeper aquifers with time. In shallow urban groundwater, MTBE generally was not found with benzene, toluene, ethylbenzene, or xylenes (BTEX) compounds which commonly are associated with gasoline spills. This disassociation causes uncertainty as to the source of MTBE. Possible sources of MTBE in groundwater include point sources, such as leaking storage tanks, and nonpoint sources, such as recharge of precipitation and storm-water runoff.

ACS Division of Environmental Chemistry, Preprints↗
USGS2010

Status and understanding of groundwater quality in the North San Francisco Bay groundwater basins, 2004: California GAMA Priority Basin Project

Groundwater quality in the approximately 1,000-square-mile (2,590-square-kilometer) North San Francisco Bay study unit was investigated as part of the Priority Basin Project of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The study unit is located in northern California in Marin, Napa, and Sonoma Counties. The GAMA Priority Basin Project is being conducted by the California State Water Resources Control Board in collaboration with the U.S. Geological Survey (USGS) and the Lawrence Livermore National Laboratory. The GAMA North San Francisco Bay study was designed to provide a spatially unbiased assessment of untreated groundwater quality in the primary aquifer systems. The assessment is based on water-quality and ancillary data collected by the USGS from 89 wells in 2004 and water-quality data from the California Department of Public Health (CDPH) database. The primary aquifer systems (hereinafter referred to as primary aquifers) were defined by the depth interval of the wells listed in the CDPH database for the North San Francisco Bay study unit. The quality of groundwater in shallower or deeper water-bearing zones may differ from that in the primary aquifers; shallower groundwater may be more vulnerable to surficial contamination. The first component of this study, the status of the current quality of the groundwater resource, was assessed by using data from samples analyzed for volatile organic compounds (VOC), pesticides, and naturally occurring inorganic constituents, such as major ions and trace elements. This status assessment is intended to characterize the quality of groundwater resources within the primary aquifers of the North San Francisco Bay study unit, not the treated drinking water delivered to consumers by water purveyors. Relative-concentrations (sample concentration divided by the health- or aesthetic-based benchmark concentration) were used for evaluating groundwater quality for those constituents that have Federal and (or) California benchmarks. A relative-concentration greater than (>) 1.0 indicates a concentration above a benchmark, and less than or equal to (≤) 1.0 indicates a concentration equal to or below a benchmark. Relative-concentrations of organic and special interest constituents were classified as “high” (relative-concentration > 1.0), “moderate” (0.1 < relative-concentration ≤ 1.0), or “low” (relative-concentration ≤ 0.1). Inorganic constituent relative-concentrations were classified as “high” (relative-concentration > 1.0), “moderate” (0.5 < relative-concentration ≤ 1.0), or “low” (relative-concentration ≤ 0.5). Aquifer-scale proportion was used as a metric for evaluating regional-scale groundwater quality. High aquifer-scale proportion is defined as the percentage of the primary aquifers that have a relative-concentration greater than 1.0; proportion is calculated on an areal rather than a volumetric basis. Moderate and low aquifer-scale proportions were defined as the percentage of the primary aquifers that have moderate and low relative-concentrations, respectively. Two statistical approaches—grid-based and spatially-weighted—were used to evaluate aquifer-scale proportion for individual constituents and classes of constituents. Grid-based and spatially-weighted estimates were comparable in the North San Francisco Bay study unit (90-percent confidence intervals). For inorganic constituents with human-health benchmarks, relative-concentrations were high in 14.0 percent of the primary aquifers, moderate in 35.8 percent, and low in 50.2 percent. The high aquifer-scale proportion of inorganic constituents primarily reflected high aquifer-scale proportions of arsenic (10.0 percent), boron (4.1 percent), and lead (1.6 percent). In contrast, relative-concentrations of organic constituents (one or more) were high in 1.4 percent, moderate in 4.9 percent, and low in 93.7 percent (not detected in 64.8 percent) of the primary aquifers. The high aquifer-scale proportion of organic constituents primarily reflected high aquifer-scale proportions of PCE (1.3 percent), TCE (0.1 percent), and 1,1-dichloroethene (0.1 percent). The inorganic constituents with secondary maximum contaminant levels (SMCL), manganese and iron, had relative-concentrations that were high in 40.8 percent and 24.4 percent of the primary aquifers, respectively. Of the 255 organic and special-interest constituents analyzed for, 26 constituents were detected. Two organic constituents were frequently detected (in 10 percent or more of samples), the trihalomethane chloroform and the herbicide simazine, but both were detected at low relative-concentrations. The second component of this study, the understanding assessment, identified the natural and human factors that affect groundwater quality by evaluating land use, physical characteristics of the wells, geochemical conditions of the aquifer, and water temperature. Results from these evaluations were used to explain the occurrence and distribution of constituents in the study unit. The understanding assessment indicated that a majority of the wells that contained nitrate also had an urban or agricultural land-use classification, had a modern or mixed age classification, and had depths to their top perforations <100 ft (30 m). Geochemical data are consistent with partial denitrification of nitrate in some reducing groundwaters in the terminal and deeper parts of the flow system. High and moderate relative-concentrations of arsenic may be attributed to reductive dissolution of manganese or iron oxides, or to desorption or inhibition of arsenic sorption under alkaline conditions. Arsenic concentrations increased with increasing depth and groundwater age in the North San Francisco Bay study unit. High to moderate relative-concentrations of boron were primarily associated with hydrothermal activity or high-salinity waters in the Napa Sonoma lowlands. Simazine was detected in groundwater classified as modern and mixed age more often than in groundwater classified as pre-modern age, while chloroform was detected most often in groundwater classified as mixed age. Simazine and chloroform also were observed in wells that had surrounding land use classified as agricultural or land use classified as urban, and top of perforation depths less than 100 ft (30 m). Together, the occurrence of chloroform and simazine in shallow wells with modern or mixed groundwater located in urban or agricultural areas suggests that these constituents result from anthropogenic activities during the last 50 years. Tritium, helium-isotope, and carbon-14 data were used to classify the predominant age of groundwater samples into three categories: modern (water that has entered the aquifer in the last 50 years), pre-modern (water that entered the aquifer more than 50 years to tens of thousands of years ago), and mixed (mixtures of modern- and pre-modern-age waters). Arsenic, iron, and total dissolved solids (TDS) concentrations were significantly greater in groundwater having pre-modern-age classification than modern, suggesting that these constituents accumulate with groundwater residence time.

California↗
USGS2023

A model of transmissivity and hydraulic conductivity from electrical resistivity distribution derived from airborne electromagnetic surveys of the Mississippi River Valley Alluvial Aquifer, Midwest USA

Groundwater-flow models require the spatial distribution of the hydraulic conductivity parameter. One approach to defining this spatial distribution in groundwater-flow model grids is to map the electrical resistivity distribution by airborne electromagnetic (AEM) survey and establish a petrophysical relation between mean resistivity calculated as a nonlinear function of the resistivity layering and thicknesses of the layers and aquifer transmissivity compiled from historical aquifer tests completed within the AEM survey area. The petrophysical relation is used to transform AEM resistivity to transmissivity and to hydraulic conductivity over areas where the saturated thickness of the aquifer is known. The US Geological Survey applied this approach to a gain better understanding of the aquifer properties of the Mississippi River Valley alluvial aquifer. Alluvial-aquifer transmissivity data, compiled from 160 historical aquifer tests in the Mississippi Alluvial Plain (MAP), were correlated to mean resistivity calculated from 16,816 line-kilometers (km) of inverted resistivity soundings produced from a frequency-domain AEM survey of 95,000 km 2 of the MAP. Correlated data were used to define petrophysical relations between transmissivity and mean resistivity by omitting from the correlations the aquifer-test and AEM sounding data that were separated by distances greater than 1 km and manually calibrating the relation coefficients to slug-test data. The petrophysical relation yielding the minimum residual error between simulated and slug-test data was applied to 2,364 line-km of AEM soundings in the 1,000-km 2 Shellmound (Mississippi) study area to calculate hydraulic property distributions of the alluvial aquifer for use in future groundwater-flow models.

Mississippi River Valley Alluvial Aquifer↗
USGS2012

Heterogeneous redox conditions, arsenic mobility, and groundwater flow in a fractured-rock aquifer near a waste repository site in New Hampshire, USA

Anthropogenic sources of carbon from landfill or waste leachate can promote reductive dissolution of in situ arsenic (As) and enhance the mobility of As in groundwater. Groundwater from residential-supply wells in a fractured crystalline-rock aquifer adjacent to a Superfund site in Raymond, New Hampshire, USA, showed evidence of locally enhanced As mobilization in relatively reducing (mixed oxic-anoxic to anoxic) conditions as determined by redox classification and other lines of evidence. Redox classification was determined from geochemical indicators based on threshold concentrations of dissolved oxygen (DO), nitrate (NO 3- ), iron (Fe 2+ ), manganese (Mn 2+ ), and sulfate (SO 4 2- ). Redox conditions were evaluated also based on methane (CH 4 ), excess nitrogen gas (N 2 ) from denitrification, the oxidation state of dissolved As speciation (As(III) and As(V)), and several stable isotope ratios. Samples from the residential-supply wells primarily exhibit mixed redox conditions, as most have long open boreholes (typically 50&ndash;100 m) that receive water from multiple discrete fractures with contrasting groundwater chemistry and redox conditions. The methods employed in this study can be used at other sites to gauge redox conditions and the potential for As mobilization in complex fractured crystalline-rock aquifers where multiple lines of evidence are likely needed to understand As occurrence, mobility, and transport.

New Hampshire↗
USGS2018

Groundwater-quality data from the eastern Snake River Plain Aquifer, Jerome and Gooding Counties, south-central Idaho, 2017

Groundwater-quality samples and water-level data were collected from 36 wells in the Jerome/Gooding County area of the eastern Snake River Plain aquifer during June 2017. The wells included 30 wells sampled for the U.S. Geological Survey’s National Water-Quality Assessment project, plus an additional 6 wells were selected to increase spatial distribution. The data provide water managers with the ability for an improved understanding of groundwater quality and flow directions in the area. Groundwater-quality samples were analyzed for nutrients, major ions, trace elements, and stable isotopes of water. Quality-assurance and quality-control measures consisted of multiple blank samples and a sequential replicate sample. All data are available online at the USGS National Water Information System.

Idaho↗
USGS2020

Inventory and analysis of groundwater resources: Theodore Roosevelt National Park, North Dakota

Industrial and commercial developments in western North Dakota potentially could affect the sources of water that contribute to wells, spring flow, and seeps within Theodore Roosevelt National Park. Without basic water resources data, accurately predicting the effects of water withdrawals and water quality concerns related to industrial and commercial developments near the park would be challenging. Water resources in the park include surface water and groundwater. The Little Missouri River and its tributaries cross all three Theodore Roosevelt National Park units and are the primary surface-water features in the park. Groundwater resources include well discharges, springs, and seeps. The geology and hydrogeology of Theodore Roosevelt National Park are defined by the surrounding Williston Basin. Four aquifers are sources of groundwater to the park: unconsolidated aquifers including alluvial systems, the upper Fort Union aquifer, the lower Fort Union aquifer, and the Fox Hills-lower Hell Creek aquifer. Data used for wells, springs, seeps, and water quality in this report were compiled from the U.S. Geological Survey National Water Information System or from the North Dakota State Water Commission. An inventory of 16 wells was completed for sites within the boundaries of the park. In addition to well data, an inventory of 11 springs and seeps was completed. The groundwater-quality analysis had two objectives: (1) to characterize the groundwater chemistry in aquifers underlying the park and (2) to spatially map selected physical properties and chemical constituents of interest. Groundwater-quality data from the North Dakota State Water Commission were summarized, mapped, and used to characterize groundwater for each aquifer in the study area. Spatial concentration distribution maps were constructed for selected physical properties and chemical constituents using summary statistics and exceedances. Piper diagrams were used to classify and characterize groundwater for each aquifer. Future research to help fill data gaps in water resources information for Theodore Roosevelt National Park, including recommendations from previous studies, consists of the following: (1) evaluating the variability in discharge from springs and seeps in comparison to changes in precipitation or other recharge sources, (2) evaluating flow control measures for flowing artesian wells, (3) completing a water rights review, and (4) performing routine water-quality monitoring for wells and springs.

North Dakota↗
USGS2001

Radiocarbon dating of dissolved inorganic carbon in groundwater from confined parts of the Upper Floridan aquifer, Florida, USA

Geochemical reaction models were evaluated to improve radiocarbon dating of dissolved inorganic carbon (DIC) in groundwater from confined parts of the Upper Floridan aquifer in central and northeastern Florida, USA. The predominant geochemical reactions affecting the 14 C activity of DIC include (1) dissolution of dolomite and anhydrite with calcite precipitation (dedolomitization), (2) sulfate reduction accompanying microbial degradation of organic carbon, (3) recrystallization of calcite (isotopic exchange), and (4) mixing of fresh water with as much as 7% saline water in some coastal areas. The calculated cumulative net mineral transfers are negligibly small in upgradient parts of the aquifer and increase significantly in downgradient parts of the aquifer, reflecting, at least in part, upward leakage from the Lower Floridan aquifer and circulation that contacted middle confining units in the Floridan aquifer system. The adjusted radiocarbon ages are independent of flow path and represent travel times of water from the recharge area to the sample point in the aquifer. Downgradient from Polk City (adjusted age 1.7 ka) and Keystone Heights (adjusted age 0.4 ka), 14 of the 22 waters have adjusted 14 C ages of 20–30 ka, indicating that most of the fresh-water resource in the Upper Floridan aquifer today was recharged during the last glacial period. All of the paleowaters are enriched in 18 O and 2 H relative to modern infiltration, with maximum enrichment in δ 18 O of approximately 2.0‰.

Hydrogeology Journal↗
USGS2006

The application of satellite differential SAR interferometry-derived ground displacements in hydrogeology

The application of satellite differential synthetic aperture radar (SAR) interferometry, principally coherent (InSAR) and to a lesser extent, persistent-scatterer (PSI) techniques to hydrogeologic studies has improved capabilities to map, monitor, analyze, and simulate groundwater flow, aquifer-system compaction and land subsidence. A number of investigations over the previous decade show how the spatially detailed images of ground displacements measured with InSAR have advanced hydrogeologic understanding, especially when a time series of images is used in conjunction with histories of changes in water levels and management practices. Important advances include: (1) identifying structural or lithostratigraphic boundaries (e.g. faults or transitional facies) of groundwater flow and deformation; (2) defining the material and hydraulic heterogeneity of deforming aquifer-systems; (3) estimating system properties (e.g. storage coefficients and hydraulic conductivities); and (4) constraining numerical models of groundwater flow, aquifer-system compaction, and land subsidence. As a component of an integrated approach to hydrogeologic monitoring and characterization of unconsolidated alluvial groundwater basins differential SAR interferometry contributes unique information that can facilitate improved management of groundwater resources. Future satellite SAR missions specifically designed for differential interferometry will enhance these contributions. ?? Springer-Verlag 2006.

Hydrogeology Journal↗
USGS2014

Feedback of land subsidence on the movement and conjunctive use of water resources

The dependency of surface- or groundwater flows and aquifer hydraulic properties on dewatering-induced layer deformation is not available in the USGS's groundwater model MODFLOW. A new integrated hydrologic model, MODFLOW-OWHM, formulates this dependency by coupling mesh deformation with aquifer transmissivity and storage and by linking land subsidence/uplift with deformation-dependent flows that also depend on aquifer head and other flow terms. In a test example, flows most affected were stream seepage and evapotranspiration from groundwater (ET gw ). Deformation feedback also had an indirect effect on conjunctive surface- and groundwater use components: Changed stream seepage and streamflows influenced surface-water deliveries and returnflows. Changed ET gw affected irrigation demand, which jointly with altered surface-water supplies resulted in changed supplemental groundwater requirements and pumping and changed return runoff. This modeling feature will improve the impact assessment of dewatering-induced land subsidence/uplift (following irrigation pumping or coal-seam gas extraction) on surface receptors, inter-basin transfers, and surface-infrastructure integrity.

Environmental Modelling and Software↗