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At least 73 records · Page 4Linked to original sources
USGS2007

Hydrogeology, Ground-Water-Age Dating, Water Quality, and Vulnerability of Ground Water to Contamination in a Part of the Whitewater Valley Aquifer System near Richmond, Indiana, 2002-2003

Assessments of the vulnerability to contamination of ground-water sources used by public-water systems, as mandated by the Federal Safe Drinking Water Act Amendments of 1996, commonly have involved qualitative evaluations based on existing information on the geologic and hydrologic setting. The U.S. Geological Survey National Water-Quality Assessment Program has identified ground-water-age dating; detailed water-quality analyses of nitrate, pesticides, trace elements, and wastewater-related organic compounds; and assessed natural processes that affect those constituents as potential, unique improvements to existing methods of qualitative vulnerability assessment. To evaluate the improvement from use of these methods, in 2002 and 2003, the U.S. Geological Survey, in cooperation with the City of Richmond, Indiana, compiled and interpreted hydrogeologic data and chemical analyses of water samples from seven wells in a part of the Whitewater Valley aquifer system in a former glacial valley near Richmond. This study investigated the application of ground-water-age dating, dissolved-gas analyses, and detailed water-quality analyses to quantitatively evaluate the vulnerability of ground water to contamination and to identify processes that affect the vulnerability to specific contaminants in an area of post-1972 greenfield development. The aquifer system in the study area includes an unconfined sand and gravel aquifer used for public-water supply (upper aquifer) and a confined sand and gravel aquifer (lower aquifer) separated by a till confining unit. Several hydrogeologic and cultural measures indicate that the upper aquifer is qualitatively vulnerable to contamination: the upper aquifer is unconfined and has a shallow depth to the water table (from about 4.75 to 14 feet below land surface), low-permeability sediments in the unsaturated zone are thin (less than 10 feet thick), estimated ground-water-flow rates through the upper aquifer are relatively rapid (the highest estimated rates ranged from 0.44 to about 5.0 feet per day), and potential contaminant sources were present. Ground-water-age dates indicate that ground-water samples represented recharge from about the time greenfield development began south of the ground-water-flow divide and that changes in water quality would lag changes in contaminant inputs. Estimates of ground-water age, computed with dichlorodifluoromethane (CFC-12) and trichlorotrifluoroethane (CFC-113) concentrations in water samples collected from seven observation wells in February and March 2003, indicated that water in the upper aquifer had recharged within about 13 to 30 years before sampling. Ground-water ages were youngest (from about 13 to 15 years since recharge) in water from the shallow wells along the glacial-valley margin and oldest (30 years) in water from a well at the base of the aquifer in the valley center. Ground-water ages determined for the shallow wells may be affected by mixing of recent recharge with older ground water from deeper in the aquifer, as indicated by upward hydraulic gradients between paired shallow and deep wells in the upper aquifer. Other parts of the Whitewater Valley aquifer system with similar hydrogeologic characteristics could be expected to have similarly young ground-water ages and residence times. Analyses of water samples collected from the seven observation wells in August and September 2002 indicated that concentrations of chloride, sodium, and nitrate generally were larger in ground water from the upper aquifer than in other parts of the Whitewater Valley aquifer system. Drinking-water-quality standards for Indiana were exceeded in water samples from one well for chloride concentrations, from four wells for dissolved-solids concentrations, and from one well for nitrate concentrations. Application of low-level methods for trace-element analyses determined that concentrations of aluminum, cobalt, iron, lithium, molybdenum, nickel, selenium, uranium, vanadium, and zinc were less than or equal to 8 micrograms per liter; concentrations of arsenic, cadmium, chromium, and copper were less than or equal to 1 microgram per liter. Application of low-level analytical methods to water samples enabled the detection of several pesticides and volatile, semivolatile, and wastewater-related organic compounds; concentrations of individual pesticides and volatile organic compounds were less than 0.1 microgram per liter and concentrations of individual wastewater organic compounds were less than 0.5 microgram per liter. The low-level analytical methods will provide useful data with which to compare future changes in water quality. Results of detailed water-quality analyses, ground-waterage dating, and dissolved-gas analyses indicated the vulnerability of ground water to specific types of contamination, the sequence of contaminant introduction to the aquifer relative to greenfield development, and processes that may mitigate the contamination. Concentrations of chloride and sodium and chloride/bromide weight ratios in sampled water from five wells indicated the vulnerability of the upper aquifer to roaddeicer contamination. Ground-water-age estimates from these wells indicated the onset of upgradient road-deicer use within the previous 25 years. Nitrate in the upper aquifer predates the post-1972 development, based on a ground-water-age date (30 years) and the nitrate concentration (5.12 milligrams per liter as nitrogen) in water from a deep well. Vulnerability of the aquifer to nitrate contamination is limited partially by denitrification. Detection of one to four atrazine transformation products in water samples from the upper aquifer indicated biological and hydrochemical processes that may limit the vulnerability of the ground water to atrazine contamination. Microbial processes also may limit the aquifer vulnerability to small inputs of halogenated aliphatic compounds, as indicated by microbial transformations of trichlorofluoromethane and trichlorotrifluoroethane relative to dichlorodifluoromethane. The vulnerability of ground water to contamination in other parts of the aquifer system also may be mitigated by hydrodynamic dispersion and biologically mediated transformations of nitrate, pesticides, and some organic compounds. Identification of the sequence of contamination and processes affecting the vulnerability of ground water to contamination would have been unlikely with conventional assessment methods.

Indiana, Ohio↗
USGS1990

Ground-water levels in water year 1987 and estimated ground-water pumpage in water years 1986-87, Carson Valley, Douglas County, Nevada

Groundwater levels were measured at 58 wells during water year 1987 and a summary of estimated pumpage is given for water years 1986 and 1987 in Carson Valley, Douglas County, Nevada. The data were collected to provide a record of groundwater changes over the long-term and pumpage estimates that can be incorporated into an existing groundwater model. The estimated total pumpage in water year 1986 was 10,200 acre-ft and in water year 1987 was 13,400 acre-ft. Groundwater levels exhibited seasonal fluctuations but remained relatively stable over the reporting period throughout most of the valley. (USGS)

Open-File Report↗
USGS1997

Water-quality assessment of the Rio Grande Valley, Colorado, New Mexico, and Texas; water-quality data for water-column, suspended-sediment, and bed-material samples collected at selected surface-water sites in the upper Rio Grande Basin, June and September 1994

As part of the Rio Grande Valley National Water-Quality Assessment Program, samples were collected at 34 sites in the upper Rio Grande Basin in Colorado and New Mexico during June and September 1994. The focus of the sampling was on trace-element concentrations in the water column, suspended sediment, and bed material. Water-column samples were analyzed for major constituent, nutrient, dissolved organic carbon, and dissolved trace- element concentrations. Suspended-sediment samples were analyzed for suspended- sediment and total trace-element concentrations. Bed-material samples were analyzed for nutrient and total trace-element concentrations. Physical properties of the water column also were measured at each site.

Open-File Report↗
USGS2002

Water quality and environmental isotopic analyses of ground-water samples collected from the Wasatch and Fort Union Formations in areas of coalbed methane development — Implications to recharge and ground-water flow, eastern Powder River Basin, Wyoming

Chemical analyses of ground-water samples were evaluated as part of an investigation of lower Tertiary aquifers in the eastern Powder River Basin where coalbed methane is being developed. Ground-water samples were collected from two springs discharging from clinker, eight monitoring wells completed in the Wasatch aquifer, and 13 monitoring or coalbed methane production wells completed in coalbed aquifers. The ground-water samples were analyzed for major ions and environmental isotopes (tritium and stable isotopes of hydrogen and oxygen) to characterize the composition of waters in these aquifers, to relate these characteristics to geochemical processes, and to evaluate recharge and ground-water flow within and between these aquifers. This investigation was conducted in cooperation with the Wyoming State Engineer's Office and the Bureau of Land Management. Water quality in the different aquifers was characterized by major-ion composition. Samples collected from the two springs were classified as calcium-sulfate-type and calcium-bicarbonate-type waters. All ground-water samples from the coalbed aquifers were sodium-bicarbonate-type waters as were five of eight samples collected from the overlying Wasatch aquifer. Potential areal patterns in ionic composition were examined. Ground-water samples collected during this and another investigation suggest that dissolved-solids concentrations in the coalbed aquifers may be lower south of the Belle Fourche River (generally less than 600 milligrams per liter). As ground water in coalbed aquifers flows to the north and northwest away from an inferred source of recharge (clinker in the study area), dissolved-solids concentrations appear to increase. Variation in ionic composition in the vertical dimension was examined qualitatively and statistically within and between aquifers. A relationship between ionic composition and well depth was noted and corroborates similar observations by earlier investigators in the Powder River Basin in both Wyoming and Montana. This relationship results in two different water-quality zones with different characteristics - a shallow zone, comprising the upper part of the Wasatch aquifer, characterized by mixed cation composition and either sulfate or bicarbonate as the dominant anion; and a deeper zone, comprising the lower (deeper) part of the Wasatch aquifer and the underlying coalbed aquifers, characterized by sodium-bicarbonate-type waters. The zonation appears to be related to geochemical processes described by earlier investigators such as dissolution and precipitation of minerals, ion exchange, sulfate reduction, and mixing of waters. Qualitative and statistically significant differences were observed in sulfate concentrations between the coalbed aquifers and the overlying Wasatch aquifer. Ionic composition suggests that bacterially mediated redox processes such as sulfate reduction were probably the dominant geochemical processes in the anaerobic coalbed aquifers. Tritium was used to qualitatively estimate the time of ground-water recharge. Tritium concentrations in both springs suggests that both were recharged after 1952 and contain modern water. Tritium was not detected at concentrations suggestive of modern water in any ground-water samples collected from the coalbed aquifers or in six of eight ground-water samples collected from the overlying Wasatch aquifer. Tritium concentrations in the remaining two wells from the Wasatch aquifer suggest a mixture between submodern (recharged before 1952) and modern water, although the low concentrations suggest that ground water in these two wells have very little modern water. The relative absence of modern water in all aquifers in the study area suggests that recharge processes to these aquifers are probably very slow. Paired d 2 H (deuterium/hydrogen isotopic ratio) and d 18 O (oxygen-18/oxygen-16 isotopic ratio) values for samples collected from the springs and all aquifers are close to the Global Meteoric Water Line, a meteoric water line for North American continental precipitation, and an estimated local meteoric water line, suggesting the water in the aquifers is of meteoric origin. The d 2 H and d 18 O values suggest that the waters were recharged in a colder climate or temperature, mid-latitudes, and mid-continent. In general, the samples do not form separate groups based on aquifer origin; this suggests either intermixing of the waters in the aquifers or that the different aquifers are subject to similar recharge and/or evolutional paths for the water. However, examination of the differences in the values of d 2 H and d 18 O, in combination with major-ion chemistry at three monitoring-well clusters, suggest that changes in the values with depth may represent different timing or sources of recharge to the different aquifers. The areal distribution of d 2 H was examined and an apparent break in the d 2 H along a northwest to southeast trend was observed. In the coalbed aquifers, all but one ground-water sample (collected from the Big George coal bed), show a pattern where the d 2 H values become more negative towards the center of the Powder River Basin and values greater (less negative) than an arbitrary reference value of -140 ‰ (per mil or parts per thousand) were observed near the outcrop area of the Wyodak-Anderson coal zone. In the overlying Wasatch aquifer, the d 2 H values became less negative towards the center of the basin. The values more negative than -140 ‰ are near the outcrop area and the values that are less negative than -140 ‰ are closer to the basin center. It is unclear if this pattern is a result of sample size, different recharge mechanisms, geochemical processes, or if the processes producing these differences are independent or unrecognized. Results of water-quality sampling were compared with selected regulatory and non-regulatory standards as well as commonly-used guidelines for proposed water uses. Dissolved solids was the measure that most frequently exceeded U.S. Environmental Protection Agency public water-supply standards and State of Wyoming domestic-use standards in ground-water samples collected from the Wasatch aquifer and coalbed aquifers. The State of Wyoming agricultural standards (irrigation) for sulfate and dissolved solids were exceeded in some samples collected from the Wasatch aquifer and coalbed aquifers. The State of Wyoming livestock standard for pH was exceeded in some samples collected from the Wasatch aquifer. Water from the Wasatch aquifer ranged from soft to very hard, and water from the coalbed aquifers ranged from moderately hard to very hard. Samples collected from wells completed in both the Wasatch aquifer and coalbed aquifers plotted in a wide range of both sodium- and salinity-hazard classes, but most samples clustered in or near the combined medium-sodium-hazard—high-salinity-hazard classes.

Wyoming↗
USGS1999

Fraser River watershed, Colorado — Assessment of available water-quantity and water-quality data through water year 1997

The water-quantity and water-quality data for the Fraser River watershed through water year 1997 were compiled for ground-water and surface-water sites. In order to assess the water-quality data, the data were related to land use/land cover in the watershed. Data from 81 water-quantity and water-quality sites, which consisted of 9 ground-water sites and 72 surface-water sites, were available for analysis. However, the data were limited and frequently contained only one or two water-quality analyses per site. The Fraser River flows about 28 miles from its headwaters at the Continental Divide to the confluence with the Colorado River. Ground-water resources in the watershed are used for residential and municipal drinking-water supplies. Surface water is available for use, but water diversions in the upper parts of the watershed reduce the flow in the river. Land use/land cover in the watershed is predominantly forested land, but increasing urban development has the potential to affect the quantity and quality of the water resources. Analysis of the limited ground-water data in the watershed indicates that changes in the land use/land cover affect the shallow ground-water quality. Water-quality data from eight shallow monitoring wells in the alluvial aquifer show that iron and manganese concentrations exceeded the U.S. Environmental Protection Agency secondary maximum contaminant level. Radon concentrations from these monitoring wells exceeded the U.S. Environmental Protection Agency proposed maximum contaminant level. The proposed radon contaminant level is currently being revised. The presence of volatile organic compounds at two monitoring wells in the watershed indicates that land use affects the shallow ground water. In addition, bacteria detected in three samples are at concentrations that would be a concern for public health if the water was to be used as a drinking supply. Methylene blue active substances were detected in the ground water at some sites and are a possible indication of contamination from wastewater. Age of the alluvial ground water ranged from 10 to 30 years; therefore, results of land-management practices to improve water quality may not be apparent for many years. Surface-water-quality data for the Fraser River watershed are sparse. The surface-water-quality data show that elevated concentrations of selected constituents generally are related to specific land uses in the watershed. For one sample (about 2 percent; 1 of 53), dissolved manganese concentration exceeded the U.S. Environmental Protection Agency secondary maximum contaminant level. Two samples from two surface-water sites in the watershed exceeded the un-ionized ammonia chronic criterion. Spatial distribution of nutrient species (ammonia, nitrite, nitrate, and total phosphorus) shows that elevated concentrations occur primarily downstream from urban areas. Sites with five or more years of record were analyzed for temporal trends in concentration of nutrient species. Downward trends were identified for ammonia and nitrite for three surface-water sites. For nitrate, no trends were observed at two sites and a downward trend was observed at one site. Total phosphorus showed no trend for the site near the mouth of the Fraser River. Downward trends in the nutrient species may reflect changes in the wastewater-treatment facilities in the watershed. Bacteria sampling completed in the watershed indicates that more bacteria are present in the water near urban settings. The limited ground-water and surface-water data for the Fraser River watershed provide a general assessment of the quantity and quality of these resources. Concentrations of most water-quality constituents generally are less than ground- and surface-water-quality standards, but the presence of bacteria, some volatile organic compounds, methylene blue active substances, and increased nutrients in the water may indicate that land use is affecting the water quality.

Colorado↗
USGS2016

Statistical analysis of lake levels and field study of groundwater and surface-water exchanges in the northeast Twin Cities Metropolitan Area, Minnesota, 2002 through 2015: Chapter A of Water levels and groundwater and surface-water exchanges in lakes of the northeast Twin Cities Metropolitan Area, Minnesota, 2002 through 2015

Water levels declined from 2003 to 2011 in many lakes in Ramsey and Washington Counties in the northeast Twin Cities Metropolitan Area, Minnesota; however, water levels in other northeast Twin Cities Metropolitan Area lakes increased during the same period. Groundwater and surface-water exchanges can be important in determining lake levels where these exchanges are an important component of the water budget of a lake. An understanding of groundwater and surface-water exchanges in the northeast Twin Cities Metropolitan Area has been limited by the lack of hydrologic data. The U.S. Geological Survey, in cooperation with the Metropolitan Council and Minnesota Department of Health, completed a field and statistical study assessing lake-water levels and regional and local groundwater and surface-water exchanges near northeast Twin Cities Metropolitan Area lakes. This report documents the analysis of collected hydrologic, water-quality, and geophysical data; and existing hydrologic and geologic data to (1) assess the effect of physical setting and climate on lake-level fluctuations of selected lakes, (2) estimate potential percentages of surface-water contributions to well water across the northeast Twin Cities Metropolitan Area, (3) estimate general ages for waters extracted from the wells, and (4) assess groundwater inflow to lakes and lake-water outflow to aquifers downgradient from White Bear Lake. Statistical analyses of lake levels during short-term (2002–10) and long-term (1925–2014) periods were completed to help understand lake-level changes across the northeast Twin Cities Metropolitan Area. Comparison of 2002–10 lake levels to several landscape and geologic characteristics explained variability in lake-level changes for 96 northeast Twin Cities Metropolitan Area lakes. Application of several statistical methods determined that (1) closed-basin lakes (without an active outlet) had larger lake-level declines than flow-through lakes with an outlet; (2) closed-basin lake-level changes reflected groundwater-level changes in the Quaternary, Prairie du Chien, and Jordan aquifers; (3) the installation of outlet-control structures, such as culverts and weirs, resulted in smaller multiyear lake-level changes than lakes without outlet-control structures; (4) water levels in lakes primarily overlying Superior Lobe deposits were significantly more variable than lakes primarily overlying Des Moines Lobe deposits; (5) lake-level declines were larger with increasing mean lake-level elevation; and (6) the frequency of some of these characteristics varies by landscape position. Flow-through lakes and lakes with outlet-control structures were more common in watersheds with more than 50 percent urban development compared to watersheds with less than 50 percent urban development. A comparison of two 35-year periods during 1925–2014 revealed that variability of annual mean lake levels in flow-through lakes increased when annual precipitation totals were more variable, whereas variability of annual mean lake levels in closed-basin lakes had the opposite pattern, being more variable when annual precipitation totals were less variable. Oxygen-18/oxygen-16 and hydrogen-2/hydrogen-1 ratios for water samples from 40 wells indicated the well water was a mixture of surface water and groundwater in 31 wells, whereas ratios from water sampled from 9 other wells indicated that water from these wells receive no surface-water contribution. Of the 31 wells with a mixture of surface water and groundwater, 11 were downgradient from White Bear Lake, likely receiving water from deeper parts of the lake. Age dating of water samples from wells indicated that the age of water in the Prairie du Chien and Jordan aquifers can vary widely across the northeast Twin Cities Metropolitan Area. Estimated ages of recharge for 9 of the 40 wells sampled for chlorofluorocarbon concentrations ranged widely from the early 1940s to mid-1970s. The wide range in estimated ages of recharge may have resulted from the wide range in the open-interval lengths and depths for the wells. Results from stable isotope analyses of water samples, lake-sediment coring, continuous seismic-reflection profiling, and water-level and flow monitoring indicated that there is groundwater inflow from nearshore sites and lake-water outflow from deep-water sites in White Bear Lake. Continuous seismic-reflection profiling indicated that deep sections of White Bear, Pleasant, Turtle, and Big Marine Lakes have few trapped gases and little organic material, which indicates where groundwater and lake-water exchanges are more likely. Water-level differences between White Bear Lake and piezometer and seepage measurements in deep waters of the lake indicate that groundwater and lake-water exchange is happening in deep waters, predominantly downgradient from the lake and into the lake sediment. Seepage fluxes measured in the nearshore sites of White Bear Lake generally were higher than seepage fluxes measured in the deep-water sites, which indicates that groundwater-inflow rates at most of the nearshore sites are higher than lake-water outflow from the deep-water sites.

Minnesota↗
USGS2007

Anthropogenic organic compounds in ground water and finished water of community water systems in the Greater Twin Cities metropolitan area, Minnesota and Wisconsin, 2004–05

As part of the U.S. Geological Survey’s National Water-Quality Assessment (NAWQA) Program, two Source Water-Quality Assessments (SWQAs) were conducted during 2004–05 in unconfined parts of the glacial aquifer system and in unconfined parts of the Prairie du Chien-Jordan aquifer in the Greater Twin Cities metropolitan area of Minnesota and Wisconsin. SWQAs are two-phased sampling activities in the NAWQA Program. The first phase evaluated the occurrence of 265 (258 are included in this report) anthropogenic organic compounds (AOCs) through monitoring source water in 30 of the largest-producing community water system wells completed in the aquifers underlying the Greater Twin Cities metropolitan area. The AOCs included volatile organic compounds (VOCs), pesticides, and other AOCs. During the second phase of the study, 15 of the original community water system wells, those with the greatest number of AOC detections, were resampled along with associated finished water. Results from the first phase of sampling indicated that 40 AOCs were detected, and 83 percent of the samples had at least one detected AOC. Concentrations of AOCs detected in the source water generally were low (defined in this report as concentrations less than 1.0 microgram per liter). Human-health benchmarks for these compounds (Maximum Contaminant Levels for regulated compounds or Health-Based Screening Levels for unregulated compounds, when they existed) typically were not exceeded. Fifteen VOCs were detected in the source-water samples. However, concentrations were low. Seventeen pesticide compounds were detected generally at concentrations less than concentrations for VOCs. Most of the pesticide compounds detected were triazine- or alachlor-parent compounds or their breakdown products. Eight other AOCs were detected in the source-water samples but generally at low concentrations. Results from the second phase of sampling indicated a total of 13 and 12 VOCs were detected in source-water and in finished-water samples, respectively. Most of the VOCs, except for those associated with disinfection by-products, were detected more frequently in source-water samples than in finished- water samples. Concentrations of most VOCs detected in either source water or finished water were less than human-health benchmarks. Twenty-one pesticide compounds were detected in either source water or finished water. Concentrations of detected pesticides in source-water and finished-water samples were low. The most frequently detected compounds in both the source and finished water were triazine-parent pesticides or their breakdown products and breakdown products of alachlor and metolachlor. In general, pesticides, if detected in source water, also were detected in the corresponding finished water. Concentrations of pesticides detected were less than human-health benchmarks in both source and finished water. A total of nine other AOCs were detected in the source-water or finished-water samples, and about the same number of compounds was detected in each of the sample groups in either source water or finished water. Detected concentrations of other AOCs were low. Water-quality results from source-water samples were compared to characterize differences between aquifers. VOC and other AOC detections were more frequent in water from the Prairie du Chien-Jordan aquifer compared to the glacial aquifer. Pesticides, however, were detected more frequently in the glacial aquifer. On the basis of study results, the hydrogeologic setting, land use, and aquifer productivity are important in explaining the occurrence of AOCs in community water system wells. Results of this study indicate that monitoring for pesticides in source water generally indicates the potential occurrence of pesticides in finished water but that this is not necessarily true of VOCs. Additional monitoring is needed to better understand the occurrence of other AOCs in source and finished waters.

Minnesota, Wisconsin↗
USGS1995

Hydrogeology, ground-water quality, and source of ground water causing water-quality changes in the Davis well field at Memphis, Tennessee

An investigation was conducted by the U.S. Geological Survey from 1992 to 1994 to collect and interpret hydrogeologic and water-quality data to determine the source of ground water causing water-quality changes in water from wells screened in the Memphis aquifer in the Davis well field at Memphis, Tennessee. Water-quality changes in aquifers used for water supply are of concern because these changes can indicate a potential for contamination of the aquifers by downward leakage from near-surface sources. The water-quality changes at the Davis well field were detected by Memphis Light, Gas and Water Division, which has periodically sampled and analyzed water from many of the 14 production wells since the well field began operation in 1971. Memphis Light, Gas and Water Division analyzed the water samples primarily for hardness, alkalinity, chloride, ulfate, and iron. Results of the e analy es and results of more recent (1992) analyse of water samples by the U.S. Geological Survey indicate that the quality of water from eight of the production wells has changed since the well field began operation. For example, from 1972 to 1991, hardness of water from one well has increased from 90 to 292 milligrams per liter (224 percent). The confining unit, which separates the fluvial deposits aquifer from the Memphis aquifer in the area of the well field, is relatively thick and contains many clay layers. However, a test hole drilled for one of five shallow wells installed in the alluvial aquifer in the Mississippi Alluvial Plain just west of the well field indicated that the confining unit separating the alluvial aquifer from the Memphis aquifer locally is absent. Differences in hydrauLic head between the alluvial and fluvial deposits aquifers and the Memphis aquifer favor downward leakage of ground water. Thus, the absence of the confining unit beneath the Mississippi Alluvial Plain just west of the well field provides a direct pathway for water in the alluvial aquifer to enter the Memphis aquifer. Comparison of selected water-quality properties and major inorganic and trace element constituent concentrations in samples from the alluvial, fluvial deposits, and Memphis aquifers indicates that the source of ground water causing waterquality changes at the Davis well field is the alluvial aquifer west of the well field . The presence of tritium and chlorofluorocarbons in water from wells screened in the Memphis aquifer in the western part of the well field indicates that relatively young (post-1940) water from the alluvial aquifer has entered the Memphis aquifer. NETPATH geochemical model code was used to mix waters from the alluvial aquifer with water from the Memphis aquifer using chloride as a conservative tracer. The resulting models indicated that a mixture containing 3 percent alluvial aquifer water mixed with 97 percent unaffected Memphis aquifer water would produce the chloride concentration measured in water from the Memphis aquifer well most affected by water-quality changes. NETPATH also was used to calculate mixing percentages of alluvial and Memphis aquifer Abstract waters based on changes in the concentrations of selected dissolved major inorganic and trace element constituents that define the dominant reactions that occur during mixing. These models indicated that a mixture containing 18 percent alluvial aquifer water and 82 percent unaffected Memphis aquifer water would produce the major constituent and trace element concentrations measured in water from the Memphis aquifer well most affected by water-quality changes. However, these model simulations predicted higher dissolved methane concentrations than were measured in water samples from the Memphis aquifer wells.

Tennessee↗
USGS2001

Ground-water hydrology and water-quality data for wells, springs, and surface-water sites in the Bradley-Brumalow creeks area near Arnold Air Force Base, Tennessee, September to December 1999

Arnold Air Force Base (AAFB) occupies about 40,000 acres in Coffee and Franklin Counties, Tennessee. The primary mission of AAFB is to support the development of aerospace systems. This mission is accomplished through test facilities at Arnold Engineering Development Center AEDC), which occupies about 4,000 acres in the center of AAFB. Several synthetic volatile organic compounds (VOC’s), primarily chlorinated solvents, have been identified in ground-water samples at AEDC. Private groundwater supplies in the Bradley-Brumalow Creeks area are hydraulically downgradient from AEDC and could be affected by transport of VOC’s in the ground water at AEDC. From September to December 1999, a comprehensive investigation of the groundwater resources in the Bradley-Brumalow Creeks area was conducted to determine if VOC’s from AEDC have affected local private water supplies and to advance understanding of the ground-water-flow system in this area. The investigation focused on locating and sampling all private water wells and springs located within the Bradley-Brumalow Creeks area that are used as a source of drinking water, though not all of the wells and springs sampled are currently used as a source of drinking water. Ground-water-flow directions were investigated by conducting base-flow stream measurements, measuring water levels in wells, and constructing a potentiometric-surface map of the Manchester aquifer in the study area. Data were collected from a total of 150 private and 88 monitoring wells during the course of the study. Depths to ground water were determined for 103 of the private wells and 86 of the monitoring wells. The wells ranged in depth from 14 to 167 feet deep. Water-level altitudes ranged from 946 to 1,081 feet above sea level. Depths to water ranged from 3 to 93 feet below land surface. Water-quality samples were collected from all 150 private wells that draw water from the Manchester aquifer. Additionally, a reconnaissance of 8 springs and 33 surface-water sites was conducted in the Bradley-Brumalow Creeks area. Discharge measurements were made at 5 of the 8 springs and all 33 of the surface-water sites as part of the regional base-flow component of the study. Water-quality samples were collected at 8 of the springs and 9 of the surface-water sites. Water-level-altitude data collected from wells and base-flow data collected from streams and springs were used to construct a regional potentiometric-surface map of the Manchester aquifer in the study area. Several notable features are illustrated on the map, including a groundwater divide that roughly follows the regional surface-water divide, a “saddle” along the groundwater divide lying northeast of AEDC, and two prominent groundwater“troughs” (valleys) extending east and southeast from the divide toward Bradley Creek. Water-quality samples collected from the 150 private wells, 8 springs, and 9 surface-water sites in the Bradley-Brumalow Creeks area were analyzed for major ions and VOC’s. The sampled water is predominantly of the calcium bicarbonate type. Specific conductance for sampled water ranged from 10 to 788 microsiemens per centimeter (µS/cm), with a median of 104 µS/cm. The range and median value for pH in sampled water were 4.5 to 8.0, and 6.3, respectively. Concentrations of most of the VOC’s analyzed for were less than detection limits. None of the sample results exceed drinking water maximum contaminant levels for public water systems. However, some compounds were detected in concentrations exceeding analytical reporting levels. Two wells produced samples containing toluene in concentrations of 1.4 and 1.3 µg/L. Chloroform also was detected in the sample from another well at a concentration of 2.4 µg/L. Other contaminants of concern were detected in estimated concentrations less than their reporting limits, referred to as estimated values. Samples from three wells showed the presence of tetrachloroethylene (PCE). Estimated concentrations of PCE in the samples ranged from 0.13 to 0.74 µg/L. Trichloroethylene (TCE) was detected in a sample from one of the three wells (0.35 µg/L). 1,1,1-Trichloroethane (1,1,1-TCA) was detected in another well (0.13 µg/L). Dichlo-rodifluoromethane was detected in samples from three other wells. Estimated concentrations of dichlorodifluoromethane ranged from 0.23 to 1.1 µg/L. Samples from another well, a spring, and a surface-water station also showed the presence of trace amounts of toluene. Estimated concentrations of toluene ranged from 0.11 to 0.47 µg/L. Benzene was detected in a sample from one well at an estimated concentration of 0.18 µg/L. Xylenes and ethylbenzene were detected in the samples from another well at estimated concentrations of 0.38 and 0.1 µg/L, respectively. For the VOC’s detected, the fre-quency of detections and median concentrations are compared to data from ambient rural ground water. Most of these volatile organic compounds, particularly the chlorinated solvents PCE, TCE, and 1,1,1-TCA, occur at concentrations above these ambient levels in the ground water at several solid waste management unit sites at AAFB. Collectively, data obtained during the study can aid in the understanding of regional ground-water-flow pathways and their relation to activities at AAFB.

Tennessee↗
USGS2008

Hydrologic, Water-Quality, and Meteorological Data for the Cambridge, Massachusetts, Drinking-Water Source Area, Water Year 2006

Records of water quantity, water quality, and meteorological parameters were continuously collected from three reservoirs, two primary streams, and four subbasin tributaries in the Cambridge, Massachusetts, drinking-water source area during water year 2006 (October 2005 through September 2006). Water samples were collected during base-flow conditions and storms in the subbasins of the Cambridge Reservoir and Stony Brook Reservoir drainage areas and analyzed for dissolved calcium, sodium, chloride, and sulfate; total nitrogen and phosphorus; and polar pesticides and metabolites. These data were collected to assist watershed administrators in managing the drinking-water source area and to identify potential sources of contaminants and trends in contaminant loading to the water supply. Monthly reservoir contents for the Cambridge Reservoir varied from about 59 to 98 percent of capacity during water year 2006, while monthly reservoir contents for the Stony Brook Reservoir and the Fresh Pond Reservoir was maintained at greater than 83 and 94 percent of capacity, respectively. If water demand is assumed to be 15 million gallons per day by the city of Cambridge, the volume of water released from the Stony Brook Reservoir to the Charles River during the 2006 water year is equivalent to an annual water surplus of about 127 percent. Recorded precipitation in the source area was about 16 percent greater for the 2006 water year than for the previous water year and was between 12 and 73 percent greater than for any recorded amount since water year 2002. The monthly mean specific-conductance values for all continuously monitored stations within the drinking-water source area were generally within the range of historical data collected since water year 1997, and in many cases were less than the historical medians. The annual mean specific conductance of 738 uS/cm (microsiemens per centimeter) for water discharged from the Cambridge Reservoir was nearly identical to the annual mean specific conductance for water year 2005 which was 737 uS/cm. However, the annual mean specific conductance at Stony Brook near Route 20 in Waltham (U.S. Geological Survey (USGS) station 01104460), on the principal tributary to the Stony Brook Reservoir, and at USGS station 01104475 on a smaller tributary to the Stony Brook Reservoir were about 15 and 13 percent lower, respectively, than the previous annual mean specific conductances of 538 and 284 uS/cm, respectively for water year 2005. The annual mean specific conductance for Fresh Pond Reservoir decreased from 553 uS/cm in the 2005 water year to 514 uS/cm in the 2006 water year. Water samples were collected in nearly all of the subbasins in the Cambridge drinking-water source area and from Fresh Pond during water year 2006. Discrete water samples were collected during base-flow conditions with an antecedent dry period of at least 4 days. Composite samples, consisting of as many as 100 subsamples, were collected by automatic samplers during storms. Concentrations of most dissolved constituents were generally lower in samples of stormwater than in samples collected during base flow; however, the average concentration of total phosphorus in samples of stormwater were from 160 to 1,109 percent greater than the average concentration in water samples collected during base-flow conditions. Concentrations of total nitrogen in water samples collected during base-flow conditions and composite samples of stormwater at USGS stations 01104415, 01104460, and 01104475 were similar, but mean concentrations of total nitrogen in samples of stormwater differed by about 0.5 mg/L (milligrams per liter) from those in water samples collected during base-flow conditions at U.S. Geological Survey stations 01104433 and 01104455. In six water samples, measurements of pH were lower than the U.S. Environmental Protection Agency (USEPA) national recommended freshwater quality criteria and the USEPA secondary drinking water-standa

Open-File Report↗
USGS1997

Regional water table (1996) and water-level changes in the Mojave River, the Morongo, and the Fort Irwin ground-water basins, San Bernardino County, California

The Mojave River, the Morongo, and the Fort Irwin ground-water basins lie in the southwestern part of the Mojave Desert Region of southern California. These basins supply ground water to local water districts, military bases, and private wells. The rapid growth in population in these basins, which is due, in part, to their proximity toLos Angeles, has increased the demand for water and, therefore, the need to understand the Mojave ground-water systems. Ground-water conditions for the Mojave River, the Morongo, and the Fort Irwin ground-water basins for 1996 and areas with significant changes in water levels are identified in this report. Water-level data were compiled for 632 wells in the study area during January-September 1996 to define the water- table surface and direction of ground-watermovement. These data were used to construct the water-table map included in this report. Also shown on the map are 31 hydrographs that show long-term water-level changes in the study area. Short-term water-level changes were determined and a water- level change map was made by comparing 1996 ground-water conditions to 1990-94 conditions in the Mojave ground-water basin and to 1994 conditions in the Morongo and the Fort Irwin ground-water basins. In general, ground-water levels and the direction of ground-water movement in the regional aquifer have not changed significantly since previously published maps (1995). However, the short-term water level did change at specific locations in all three ground-water basins. Water levels in the Mojave River ground-water basin had a maximum rise during the period 1992-96 of 52 feet and a maximum decline of 28. Water levels in the Morongo ground-water basin had a maximum rise of 66 feet and a maximum decline of 57 feet. The Fort Irwin ground-water basins, however, had relatively little change in water level with a maximum rise of 6 feet and a maximum decline of 8 feet. Hydrographs in the regional aquifer systemindicate a decline or, in some areas, no change in the water table during the period of record. Water levels in the shallow alluvial aquifer, generally within 1 mile of the Mojave River, fluctuate in response to streamflow. Ground-water levels rise during wet periods, when floodflows in the Mojave River recharge the shallow alluvial aquifer.

California↗
USGS2005

Questa baseline and pre-mining ground-water quality investigation. 5. Well installation, water-level data, and surface- and ground-water geochemistry in the Straight Creek drainage basin, Red River Valley, New Mexico, 2001-03

The U.S. Geological Survey, in cooperation with the New Mexico Environment Department, is investigating the pre-mining ground-water chemistry at the Molycorp molybdenum mine in the Red River Valley, northern New Mexico. The primary approach is to determine the processes controlling ground-water chemistry at an unmined, off-site, proximal analog. The Straight Creek drainage basin, chosen for this purpose, consists of the same quartz-sericite-pyrite altered andesitic and rhyolitic volcanic rock of Tertiary age as the mine site. The weathered and rugged volcanic bedrock surface is overlain by heterogeneous debris-flow deposits that interfinger with alluvial deposits near the confluence of Straight Creek and the Red River. Pyritized rock in the upper part of the drainage basin is the source of acid rock drainage (pH 2.8-3.3) that infiltrates debris-flow deposits containing acidic ground water (pH 3.0-4.0) and bedrock containing water of circumneutral pH values (5.6-7.7). Eleven observation wells were installed in the Straight Creek drainage basin. The wells were completed in debris-flow deposits, bedrock, and interfingering debris-flow and Red River alluvial deposits. Chemical analyses of ground water from these wells, combined with chemical analyses of surface water, water-level data, and lithologic and geophysical logs, provided information used to develop an understanding of the processes contributing to the chemistry of ground water in the Straight Creek drainage basin. Surface- and ground-water samples were routinely collected for determination of total major cations and selected trace metals; dissolved major cations, selected trace metals, and rare-earth elements; anions and alkalinity; and dissolved-iron species. Rare-earth elements were determined on selected samples only. Samples were collected for determination of dissolved organic carbon, mercury, sulfur isotopic composition (34S and 18O of sulfate), and water isotopic composition (2H and 18O) during selected samplings. One set of ground-water samples was collected for helium-3/tritium and chlorofluorocarbon (CFC) age dating. Several lines of evidence indicate that surface water is the primary input to the Straight Creek ground-water system. Straight Creek streamflow and water levels in wells closest to the apex of the Straight Creek debris fan and closest to Straight Creek itself appear to respond to the same seasonal inputs. Oxygen and hydrogen isotopic compositions in Straight Creek surface water and ground water are similar, and concentrations of most dissolved constituents in most Straight Creek surface-water and shallow (debris-flow and alluvial) aquifer ground-water samples correlate strongly with sulfate (concentrations decrease linearly with sulfate in a downgradient direction). After infiltration of surface water, dilution along the flow path is the dominant mechanism controlling ground-water chemistry. However, concentrations of some constituents can be higher in ground water than can be accounted for by concentrations in Straight Creek surface water, and additional sources of these constituents must therefore be inferred. Constituents for which concentrations in ground water can be high relative to surface water include calcium, magnesium, strontium, silica, sodium, and potassium in ground water from debris-flow and alluvial aquifers and manganese, calcium, magnesium, strontium, sodium, and potassium in ground water from the bedrock aquifer. All ground water is a calcium sulfate type, often at or near gypsum saturation because of abundant gypsum in the aquifer material developed from co-existing calcite and pyrite mineralization. Calcite dissolution, the major buffering mechanism for bedrock aquifer ground water, also contributes to relatively higher calcium concentrations in some ground water. The main source of the second most abundant cation, magnesium, is probably dissolution of magnesium-rich carbonates or silicates.

New Mexico↗
USGS1997

Hydrogeology, water quality, and simulation of ground-water-development alternatives in the Usquepaug-Queen ground-water reservoir, southern Rhode Island

The Usquepaug-Queen River Basin study describes the hydrogeology, water quality, and simulation of pumping from wells for selected ground-water-development alternatives in the ground-water reservoir under average (1975-90) and drought (1963-66) conditions. In general, ground-water quality is suitable for most purposes. The study provides an evaluation of the effects of simulated pumping of 4 to 11 million gallons per day of ground water on the stream-wetland-aquifer system. Three principal geologic units underlie the Usquepaug-Queen River Basin glacial stratified deposits (stratified drift), glacial till, and crystalline bedrock. Thick and extensive deposits of saturated coarse-grained stratified deposits form the major and most productive aquifer in the Usquepaug-Queen River Basin. The 36.1-square mile Usquepaug-Queen River Basin is in the Pawcatuck River Basin in southern Rhode Island. Stratified deposits cover about 42 percent of the basin and reach a maximum known thickness of 122 feet. The stratified deposits are subdivided into coarse-grained units (dominantly fine to very coarse sand and gravel) and fine-grained units (dominantly very fine sand, silt, and clay). Transmissivity is highest in coarse-grained stratified materials, which have the capability of yielding relatively high volumes of water to wells. Transmissivity is lowest in fine-grained stratified materials, which consist predominantly of lakebottom deposits. Transmissivity of the stratified drift aquifer ranges from 1,900 to 27,800 feet squared per day, and horizontal hydraulic conductivity ranges from 25 to 470 feet per day. The stratified-drift aquifer is the only aquifer in the Usquepaug-Queen River Basin capable of producing yields of 0.5 million gallons per day or more from individual wells. Pumping from ground-water and surface-water sources in the Usquepaug-Queen River Basin averaged 0.28 million gallons per day during 1989 and 0.48 million gallons per day during 1990. Ground water and surface water (which is primarily ground-water runoff) in the UsquepaugQueen River Basin are suitable for most purposes on the basis of a comparison of physical properties and chemical constituents to drinking-water standards. Ground water in the basin is somewhat corrosive because of its low hydrogen-ion concentration. Specific conductance and concentrations of dissolved chloride and dissolved sodium are high in ground water in parts of the Usquepaug-Queen River Basin, which indicates the effects of highway de-icing salts on groundwater quality. Nitrogen (nitrite plus nitrate) concentrations in some localized areas exceed the U.S. Environmental Protection Agency maximum contaminant level of 10 milligrams per liter for drinking water. The effects of selected ground-waterdevelopment alternatives on ground-water levels, wetland-water levels, and streamflow in the Usquepaug-Queen ground-water reservoir were evaluated by means of a three-layer ground-waterflow model. Development alternatives were simulated for average annual (1975-90) and drought (1963-66) conditions. In general, higher simulated pumping rates produced greater drawdowns than lower pumping rates. Drawdowns generally can be reduced by distributing the total pumping over many wells; however, drawdowns were minimal (less than 1.3 feet) in well SNW 906, which was near a major stream (recharge boundary); and drawdowns were substantial (at least 12 feet) in well EXW 33, which was near the edge of the model aquifer boundary (barrier boundary). Total gains in flow from ground-water discharge for all streams in the model area were not affected by the location of wells; however, the amount of ground-water pumpage derived from induced infiltration of streamflow varies significantly. Water levels in the wetlands tend to be constant even during simulated pumping. In general, pumping during simulated drought conditions increased drawdowns fractionally and greatly reduced overall streamflow gains. Pumping from the Usquepaug-Queen stratified-drift aquifer causes infiltration of streamflow along stream segments simulated in the ground-water-flow model. Results of simulations for average conditions show that from 56 to 75 percent of the total water pumped is derived from intercepted ground-water runoff and that the amount of well water derived from induced recharge of streamflow ranged from 20 to 39 percent. The areal extent of contributing areas for selected simulated pumping wells suggest that large areas of stratified drift may need to be protected from land-use practices that are incompatible with the development of potable ground water in the Usquepaug-Queen ground-water reservoir.

Rhode Island↗
USGS2010

Concentration data for anthropogenic organic compounds in groundwater, surface water, and finished water of selected community water systems in the United States, 2002-10

The National Water-Quality Assessment Program of the U.S. Geological Survey began implementing Source Water-Quality Assessments (SWQAs) in 2001 that focus on characterizing the quality of source water and finished water of aquifers and major rivers used by some of the larger community water systems in the United States. As used in SWQA studies, source water is the raw (ambient) water collected at the supply well before water treatment (for groundwater) or the raw (ambient) water collected from the river near the intake (for surface water), and finished water is the water that has been treated and is ready to be delivered to consumers. Finished-water samples are collected before the water enters the distribution system. The primary objective of SWQAs is to determine the occurrence of more than 250 anthropogenic organic compounds in source water used by community water systems, many of which currently are unregulated in drinking water by the U.S. Environmental Protection Agency. A secondary objective is to understand recurrence patterns in source water and determine if these patterns also occur in finished water before distribution. SWQA studies were conducted in two phases for most studies completed by 2005, and in one phase for most studies completed since 2005. Analytical results are reported for a total of 295 different anthropogenic organic compounds monitored in source-water and finished-water samples collected during 2002-10. The 295 compounds were classified according to the following 13 primary use or source groups: (1) disinfection by-products; (2) fumigant-related compounds; (3) fungicides; (4) gasoline hydrocarbons, oxygenates, and oxygenate degradates; (5) herbicides and herbicide degradates; (6) insecticides and insecticide degradates; (7) manufacturing additives; (8) organic synthesis compounds; (9) pavement- and combustion-derived compounds; (10) personal-care and domestic-use products; (11) plant- or animal-derived biochemicals; (12) refrigerants and propellants; and (13) solvents. This report presents the analytical results of source- water samples from 448 community water system wells and 21 surface-water sites. This report also presents the analytical results of finished-water samples from 285 wells and 20 surface-water sites from community water systems. Results of quality-assurance/quality-control samples also are presented including data for equipment blanks, field blanks, source solution blanks, and replicate samples.

Data Series↗
USGS2013

Water-quality conditions, and constituent loads and yields in the Cambridge drinking-water source area, Massachusetts, water years 2005–07

The source water area for the drinking-water supply of the city of Cambridge, Massachusetts, encompasses major transportation corridors, as well as large areas of light industrial, commercial, and residential land use. Because of ongoing development in the drinking-water source area, the Cambridge water supply has the potential to be affected by a wide variety of contaminants. The U.S. Geological Survey (USGS) has monitored surface-water quality in the Hobbs Brook and Stony Brook Basins, which compose the drinking-water source area, since 1997 (water year 1997) through continuous monitoring and discrete sample collection and, since 2004, through systematic collection of streamwater samples during base-flow and stormflow conditions at five primary sampling stations in the drinking-water source area. Four primary sampling stations are on small tributaries in the Hobbs Brook and Stony Brook Basins; the fifth primary sampling station is on the main stem of Stony Brook and drains about 93 percent of the Cambridge drinking-water source area. Water samples also were collected at six secondary sampling stations, including Fresh Pond Reservoir, the final storage reservoir for the raw water supply. Storm runoff and base-flow concentrations of calcium (Ca), chloride (Cl), sodium (Na), and sulfate (SO 4 ) were estimated from continuous records of streamflow and specific conductance for six monitoring stations, which include the five primary sampling stations. These data were used to characterize current water-quality conditions, estimate loads and yields, and describe trends in Cl and Na in the tributaries and main-stem streams in the Hobbs Brook and Stony Brook Basins. These data also were used to describe how streamwater quality is affected by various watershed characteristics and provide information to guide future watershed management. Water samples were analyzed for physical properties and concentrations of Ca, Cl, Na, and SO 4 , total nitrogen (TN), total phosphorus (TP), caffeine, and a suite of 59 polar pesticides. Values of physical properties and constituent concentrations varied widely, particularly in samples from tributaries. Median concentrations of Ca, Cl, Na, and SO4 in samples collected in the Hobbs Brook Basin (39.8, 392, 207, and 21.7 milligrams per liter (mg/L), respectively) were higher than those for the Stony Brook Basin (17.8, 87.7, 49.7, and 14.7 mg/L, respectively). These differences in major ion concentrations are likely related to the low percentages of developed land and impervious area in the Stony Brook Basin. Concentrations of dissolved Cl and Na in samples, and those estimated from continuous records of specific conductance (particularly during base flow), often were greater than the U.S. Environmental Protection Agency (USEPA) secondary drinking-water guideline for Cl (250 mg/L), the chronic aquatic-life guideline for Cl (230 mg/L), and the Commonwealth of Massachusetts, Executive Office of Energy and Environmental Affairs drinking-water guideline for Na (20 mg/L). Mean annual flow-weighted concentrations of Ca, Cl, and Na were generally positively correlated with the area of roadway land use in the subbasins. Correlations between mean annual concentrations of Ca and SO 4 in base flow and total roadway, total impervious, and commercial-industrial land uses were statistically significant. Concentrations of TN (range of 0.42 to 5.13 mg/L in all subbasins) and TP (range of 0.006 to 0.80 mg/L in all subbasins) in tributary samples did not differ substantially between the Hobbs Brook and Stony Brook Basins. Concentrations of TN and TP in samples collected during water years 2004–07 exceeded proposed reference concentrations of 0.57 and 0.024 mg/L, in 94 and 56 percent of the samples, respectively. Correlations between annual flow-weighted concentrations of TN and percentages of recreational land use and water-body area were statistically significant; however, no significant relation was found between TP and available land-use information. The volume of streamflow affected water-quality conditions at the primary sampling stations. Turbidity and concentrations of TP were positively correlated with streamflow. In contrast, concentrations of major ions were negatively correlated with streamflow, indicating that these constituents were diluted during stormflows. Concentrations of TN were not correlated with streamflow. Twenty-five pesticides and caffeine were detected in water samples collected in the drinking-water source area and in raw water collected from the Cambridge water-treatment facility intake at the Fresh Pond Reservoir. Imidacloprid, norflurazon, and siduron were the most frequently detected pesticides with the frequency of detections ranging from about 24 to 41 percent. Caffeine was detected in about 37 percent of water samples at concentrations ranging from 0.003 to 1.82 micrograms per liter (μg/L). Although some of the detected pesticides degrade rapidly, norflurazon and siduron are relatively stable and are able to immigrate though the serial reservoir system. Concentrations of 2,4-D, carbaryl, imazaquin, MCPA (2-methyl-4-chlorophenoxyacetic acid), metsulfuron-methyl, norflurazon, siduron, and caffeine were detected more frequently in stormflow samples than in base-flow samples. Concentrations of pesticides did not exceed USEPA drinking-water guidelines or other health standards and were several orders of magnitude less than the lethal exposure level established for several fish species common to the drinking-water source area. Imidacloprid, an insecticide, was the only pesticide with a concentration exceeding available long-term aquatic-life guidelines. Several pesticides correlated significantly with the amount of recreational, residential, and commercial area in the tributary subbasins. Mean annual base-flow concentrations of caffeine correlated significantly with parking-lot land use. For most tributaries, about 70 percent of the annual loads of Ca, Cl, Na, and SO 4 were associated with base flow. Upward temporal trends in annual loads of Cl and Na were identified on the basis of data for water years 1998 to 2008 for the outlet of the Cambridge Reservoir in the Hobbs Brook Basin; however, similar trends were not identified for the main stem of Stony Brook downstream from the reservoir. The proportions of the TN load attributed to base flow and stormflow were similar in each tributary. In contrast, more than 83 percent of the TP loads in the tributaries and about 73 percent of the TP load in main stem of Stony Brook were associated with stormflow. Mean annual yields of Ca, Cl, Na, and SO 4 in the Stony Brook Reservoir watershed, which represents most of the drinking-water source area, were 14, 85, 46, and 9 metric tons per square kilometer, respectively. Mean annual yields among the individual tributary subbasins varied extensively. Mean annual yields for the respective constituents increased with an increase in roadway and parking-lot area in the tributary subbasins. Mean annual yields of TN in the tributary subbasins ranged from about 740 to more than 1,200 kilograms per square kilometer and exceeded the yield for the main stem of Stony Brook at USGS station 01104460 upstream from the Stony Brook Reservoir. Mean annual yields estimated for the herbicides 2,4-D and imidacloprid ranged from 34 to 310 grams per square kilometer (g/km 2 ) and 3 to 170 g/km 2 , respectively. Annual loads for 2,4-D were entirely associated with stormflow. The largest annual load for imidacloprid was estimated for the main stem of Stony Brook; however, the highest annual yield for this pesticide, as well as for benomyl, carbaryl, metalaxyl, and propiconazole, was estimated for a tributary to the Stony Brook Reservoir that drains largely residential and recreational areas. Mean annual yields for the herbicide siduron ranged from 6.9 to 35 g/km 2 with most of the loads associated with stormflow. Mean annual yields for the insecticide diuron ranged from 2.1 to 4.4 g/km 2 . Annual yields of caffeine ranged from 11 to 410 g/km 2 .

Massachusetts↗
USGS2020

Compounds of emerging concern detected in water samples from potable water and wastewater treatment plants and detected in water and bed-sediment samples from sites on the Trinity River, Dallas, Texas, 2009–13

The population in the Dallas-Fort Worth metropolitan area in northern Texas is rapidly growing, resulting in a rapid increase in the demand for potable water and an increase in the discharge of wastewater treatment plant effluent. An assessment of compounds of emerging concern (CECs) in samples collected at potable water and wastewater treatment plants in Dallas and downstream from Dallas in the Trinity River was completed by the U.S. Geological Survey in cooperation with the City of Dallas, Dallas Water Utilities. CECs are synthetic or naturally occurring chemicals that are not commonly monitored in the environment but can enter the environment and cause known or suspected adverse ecological or human health effects. CECs can enter the environment through nonpoint sources (for example, runoff) and point sources (for example, concentrated animal feeding operations and treated-effluent discharge from wastewater treatment plants), which can increase concentrations of CECs especially in highly populated areas. CECs include pharmaceuticals (prescription and nonprescription), steroidal hormones, stanols, sterols, detergents and detergent metabolites (hereinafter referred to as “detergents”), personal-use products, pesticides, polycyclic aromatic hydrocarbons (PAHs), flame retardants, plasticizers, and other organic compounds used in everyday domestic, agricultural, and industrial applications. The release of CECs to the environment went largely unrecognized until relatively recently. Increased loading of certain CECs to the environment, combined with advancements in laboratory analysis methods that resulted in appreciably lower detection levels, brought greater attention to the release of CECs. In addition, synthesis of new chemicals or changes in use and disposal of existing chemicals can create new sources of CECs. Some CECs are endocrine disrupting compounds (EDCs), which can elicit adverse effects on development, behavior, and reproduction of wildlife and can cause dysfunction of human and wildlife endocrine (hormone) systems. Results of studies in the United States and Europe indicate that CECs, their metabolites, and industrial, agricultural, and household wastewater products are present in the aquatic environment, water treatment plants, and septic systems. CECs, especially pharmaceuticals, are of interest because of their persistence, widespread use, and potential to cause adverse effects in humans and nontargeted organisms. There is also concern that some CECs and EDCs resist degradation of water treatment processes at potable water treatment plants (PWTPs) and wastewater treatment plants (WWTPs) and that treated-effluent discharge could contain compounds that negatively affect biota living in receiving waters. Therefore, CECs and EDCs are more likely to be detected in environmental samples collected near areas of high population density where treated effluent from WWTPs can contribute substantially to receiving waters. The U.S. Geological Survey, in cooperation with the City of Dallas, Dallas Water Utilities, evaluated the occurrence and concentrations of selected CECs in samples collected at PWTPs and WWTPs in Dallas and downstream from the Dallas-Fort Worth metropolitan area in the Trinity River, Texas, from August 2009 to December 2013. Water samples were collected at three PWTP sites, two WWTP sites, and five study sites on the Trinity River; all sites where samples were collected were in or downstream from Dallas. These water samples were analyzed for 120 CECs, including human-health pharmaceuticals (prescription and nonprescription), antibiotics, steroidal hormones, stanols, sterols, detergents, personal-use products (flavors and fragrances), pesticides and repellents, industrial wastewater compounds, disinfection compounds, PAHs, flame retardants, and plasticizers. Additionally, bed-sediment samples were collected at each of the five Trinity River sites. The bed-sediment samples were analyzed for 57 CECs. In general, the water treatment processes at PWTPs and WWTPs were effective at reducing detections and concentrations of CECs to undetectable levels or transforming the compounds into degradates that were not analyzed. There were 14 and 73 CECs detected in raw water and in untreated-influent water at PWTPs and WWTPs, respectively. Of these, 11 of the 14 CECs detected in raw-water samples and 44 of the 73 CECs detected in untreated-influent samples were not detected in finished water or in treated-effluent water samples, respectively, indicating that these compounds were removed or degraded to compounds that were not analyzed. Some CECs, however, are resistant to degradation and were detected in untreated and treated water at PWTPs and at WWTPs. The three CECs detected at PWTPs in raw-water and finished-water samples were tris(dichloroisopropyl)phosphate, benzophenone, and methyl salicylate. At WWTPs, 29 CECs were detected, including carbamazepine, sulfamethoxazole, 4-androstene-3,17- dione , 3-beta-coprostanol, acetyl-hexamethyl-tetrahydronaphthalene (AHTN), hexahydro-hexamethyl-cyclopenta-benzopyran (HHCB), 1,4-dichlorobenzene, tribromomethane, benzophenone, and tris(dichloroisopropyl)phosphate, in untreated and treated water, indicating that treatment processes likely did not remove or degrade these compounds. Of the 23 CECs detected in stream-water samples collected at 5 sites on the Trinity River in or near Dallas, 10 CECs (carbamazepine, sulfamethoxazole, caffeine, 3-beta-coprostanol, cholesterol, HHCB, benzophenone, triethyl citrate, tributyl phosphate, and tris(dichloroisopropyl)phosphate) were detected at all 5 sites. The 10 CECs detected in water samples collected at all 5 sites on the Trinity River were also detected in treated-effluent water at WWTPs. Eleven of the 57 targeted CECs were detected in bed-sediment samples collected at study sites on the Trinity River. Of these 11 CECs, only 2 (beta-sitosterol and cholesterol) were detected in bed-sediment samples at all 5 sites on the Trinity River. Nine of these 11 CECs were not detected in any water-column sample, likely because of the strong hydrophobic characteristics of these compounds. Results from water treatment plants indicate that the water treatment process is less effective for removing or degrading compounds that are engineered to be resistant to degradation. These results also indicate the presence of CECs and EDCs at locations upstream from PWTPs in Dallas. Results from Trinity River main-stem sites indicate that some compounds are naturally attenuated during transport, but a few are persistent throughout the study reach. Many CECs and EDCs are hydrophobic and were only detected in bed sediment, indicating multiple pathways through which CECs can persist in the environment. In general, concentrations of CECs in the Dallas-Fort Worth metropolitan area were similar to those found in metropolitan areas nationwide.

Texas↗
USGS2002

Spatial patterns and temporal variability in water quality from City of Albuquerque drinking-water supply wells and piezometer nests, with implications for the ground-water flow system

Water-quality data for 93 City of Albuquerque drinking-water supply wells, 7 deep piezometer nests, and selected additional wells were examined to improve understanding of the regional ground-water system and its response to pumpage. Plots of median values of several major parameters showed discernible water-quality differences both areally and with depth in the aquifer. Areal differences were sufficiently large to enable delineation of five regions of generally distinct water quality, which are consistent with areas of separate recharge defined by previous investigators. Data for deep piezometer nests indicate that water quality generally degrades somewhat with depth, except in areas where local recharge influenced by evapotranspiration or contamination could be affecting shallow water. The orientations of the five water-quality regions indicate that the direction of ground-water flow has historically been primarily north to south. This is generally consistent with maps of predevelopment hydraulic heads, although some areas lack consistency, possibly because of differences in time scales or depths represented by water quality as opposed to hydraulic head. The primary sources of recharge to ground water in the study area appear to be mountain-front recharge along the Sandia Mountains to the east and the Jemez Mountains to the north, seepage from the Rio Grande, and infiltration through Tijeras Arroyo. Elevated concentrations of many chemical constituents in part of the study area appear to be associated with a source of water having large dissolved solids, possibly moving upward from depth. Hydraulic-head data for deep piezometer nests indicate that vertical head gradients differ in direction and magnitude across the study area. Hydraulic-head gradients are downward in the central and western parts of the study area and upward across much of the eastern part, except at the mountain front. Water-quality data for the piezometers indicate that the ground water is not well mixed, even in areas of large vertical gradients. Water levels in most piezometers respond to short-term variations in ground-water withdrawals and to the cumulative effect of long-term withdrawals throughout the area. In most piezometers screened below the water table, water levels respond clearly to seasonal variations in ground-water withdrawals. Water levels decline from about April through July and rise from about September through January. Water levels seem to be declining in most piezometers at a rate less than 1 foot per year. Water-quality data for unfiltered samples collected over a 10-year period from 93 City of Albuquerque drinking-water supply wells were examined for variability and temporal trends in 10 selected parameters. Variability generally was found to be greatest in the Western and Northeast water-quality regions of the study area. For the 10 parameters investigated, temporal trends were found in 5 to 57 wells. Dissolved-solids, sodium, sulfate, chloride, and silica concentrations showed more increasing than decreasing trends; calcium, bicarbonate, and arsenic concentrations, field pH, and water temperature showed more decreasing than increasing trends. The median magnitudes of most of these trends over a 1-year period were not particularly large (generally less than 1.0 milligram per liter), although the magnitudes for a few individual wells were significant. For the 10 parameters investigated, correlations with monthly pumpage volumes were found in 10 to 32 wells. Calcium and sulfate concentrations, field pH, and water temperature showed more positive than negative correlations with monthly pumpage; dissolved-solids, sodium, bicarbonate, chloride, silica, and arsenic concentrations showed more negative than positive correlations.

New Mexico↗
USGS2004

Regional water table (2004) and water-level changes in the Mojave River and Morongo ground-water basins, Southwestern Mojave Desert, California

The Mojave River and Morongo ground-water basins are in the southwestern part of the Mojave Desert in southern California. Ground water from these basins supplies a major part of the water requirements for the region. The continuous population growth in this area has resulted in ever-increasing demands on local ground-water resources. The collection and interpretation of ground-water data helps local water districts, military bases, and private citizens gain a better understanding of the ground-water flow systems, and consequently, water availability. During March and April 2004, the U.S. Geological Survey and other agencies made almost 900 water-level measurements in about 740 wells in the Mojave River and Morongo ground-water basins. These data document recent conditions and, when compared with historical data, changes in ground-water levels. A water-level contour map was drawn using data from 500 wells, providing coverage for most of the basins. In addition, 26 long-term (as much as 74 years) hydrographs were constructed which show water-level conditions throughout the basins, 9 short-term (1992 to 2004) hydrographs were constructed which show the effects of recharge and discharge along the Mojave River, and a water-level-change map was compiled to compare 2002 and 2004 water levels throughout the basins. The water-level change data show that in the Mojave River ground-water basin, more than one half (102) of the wells had water-level declines of 0.5 ft or more and almost one fifth (32) of the wells had declines greater than 5 ft. between 2002 and 2004. The water-level change data also show that about one tenth (17) of the wells compared in the Mojave River ground-water basin had water level increases of 0.5 ft or more. Most of the water-level increases were the result of stormflow in the Mojave River during March 2004, which resulted in recharge to wells in the floodplain aquifer mainly along the river in the Alto subarea and the Transition zone, and along the river east of Barstow. In the Morongo ground-water basin, nearly one half (55) of the wells had water-level declines of 0.5 ft or more, and about one tenth (13) of the wells had declines greater than 5 ft. The Warren subbasin, where artificial-recharge operations in Yucca Valley (pl. 1) have caused water levels to rise, had water-level increases of as much as about 97 ft since 2002.

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