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USGS2023

Quality of groundwater used for domestic supply in the Modesto, Turlock, and Merced Subbasins of the San Joaquin Valley, California

Summary More than 2 million Californians rely on groundwater from privately owned domestic wells for drinking-water supply. This report summarizes a water-quality survey of domestic and small-system drinking-water supply wells in the Modesto, Turlock, and Merced subbasins of the San Joaquin Valley where more than 78,000 residents are estimated to use privately owned domestic wells. Results indicate that inorganic and organic constituents in groundwater were respectively present above regulatory (maximum contaminant level, MCL) benchmarks for public drinking-water quality in 37 percent and 9 percent of the aquifer area used for domestic drinking-water supplies (herein, “domestic groundwater resources”). The most prevalent inorganic constituents exceeding regulatory benchmarks were nitrate, uranium, and arsenic. The only organic constituents exceeding regulatory benchmarks were the fumigant constituents 1,2,3-trichloropropane (1,2,3-TCP) and 1,2-dibromo-3-chloropropane (DBCP), but the herbicides atrazine and simazine were detected at low concentrations below one-tenth of regulatory benchmarks in 30 percent of domestic groundwater resources. Total dissolved solids (TDS) and manganese exceeded aesthetic-based (secondary maximum contaminant level [SMCL]) benchmarks for drinking water in 3 percent and 13 percent of domestic groundwater resources, respectively. Per- and polyfluoroalkyl substances (PFAS) were detected in 23 percent of domestic groundwater resources, with 4 percent exceeding California state notification or response levels for specific compounds. Total coliform bacteria were detected in 20 percent of domestic groundwater resources. Elevated concentrations of nitrate, uranium, TDS, and pesticides (fumigant constituents and herbicides) are related to agricultural land use and were typically present at shallow depths up to 75 meters below land surface. Agriculturally derived constituents were detected in wells screened below the Corcoran Clay Member of the Tulare Formation (herein, “Corcoran Clay”) in the southeastern part of the study area, where the Corcoran Clay tends to be shallower and thinner than in areas to the northwest. Nitrate, uranium, and TDS were most prevalent in the northwest part of the study area proximal to the valley trough where soils are poorly drained and agricultural land uses are predominantly grain, alfalfa, and dairy farms. Pesticides tended to occur in groundwater below coarse-grained surficial deposits and within a northwest to southeast trending band along the eastern extent of the Corcoran Clay that typically demarcates the western extent of well-drained soils associated with perennial orchard crops. Elevated concentrations of arsenic tended to occur west of this band in reducing groundwater but also sometimes co-occurred with elevated nitrate in oxic groundwater, most likely because of geochemical conditions in agriculturally affected groundwater that can enhance the mobility of arsenic from aquifer sediments.

California↗

USGS2009

Impact of wildfire on levels of mercury in forested watershed systems: Voyageurs National Park, Minnesota

Atmospheric deposition of mercury to remote lakes in mid-continental and eastern North America has increased approximately threefold since the mid-1800s (Swain and others, 1992; Fitzgerald and others, 1998; Engstrom and others, 2007). As a result, concerns for human and wildlife health related to mercury contamination have become widespread. Despite an apparent recent decline in atmospheric deposition of mercury in many areas of the Upper Midwest (Engstrom and Swain, 1997; Engstrom and others, 2007), lakes in which fish contain levels of mercury deemed unacceptable for human consumption and possibly unacceptable for fish-consuming wildlife are being detected with increasing frequency. In northern Minnesota, Voyageurs National Park (VNP) (fig. 1) protects a series of southern boreal lakes and wetlands situated on bedrock of the Precambrian Canadian Shield. Mercury contamination has become a significant resource issue within VNP as high concentrations of mercury in loons, bald eagle eaglets, grebes, northern pike, and other species of wildlife and fish have been found. The two most mercury-contaminated lakes in Minnesota, measured as methylmercury in northern pike ( Esox lucius ), are in VNP. Recent multidisciplinary U.S. Geological Survey (USGS) research demonstrated that the bulk of the mercury in lake waters, soils, and fish in VNP results from atmospheric deposition (Wiener and others, 2006). The study by Wiener and others (2006) showed that the spatial distribution of mercury in watershed soils, lake waters, and age-1 yellow perch ( Perca flavescens ) within the Park was highly variable. The majority of factors correlated for this earlier study suggested that mercury concentrations in lake waters and age-1 yellow perch reflected the influence of ecosystem processes that affected within-lake microbial production and abundance of methylmercury (Wiener and others, 2006), while the distribution of mercury in watershed soils seemed to be partially dependent on forest disturbance, especially the historic forest fire pattern (Woodruff and Cannon, 2002). Forest fire has an essential role in the forest ecosystems of VNP (Heinselman, 1996). Because resource and land managers need to integrate both natural wildfire and prescribed fire in management plans, the potential influence of fire on an element as sensitive to the environment as mercury becomes a critical part of their decisionmaking. A number of recent studies have shown that while fire does have a significant impact on mercury at the landscape level, the observed effects of fire on aquatic environments are highly variable and unpredictable (Caldwell and others, 2000; Garcia and Carrigan, 2000; Kelly and others, 2006; Nelson and others, 2007). Caldwell and others (2000) described an increase in methylmercury in reservoir sediments resulting from mobilization and transport of charred vegetative matter following a fire in New Mexico. Krabbenhoft and Fink (2000) attributed increases in total mercury concentrations in young-of-the-year fish in the Florida Everglades to release of mercury resulting from peat oxidation following fires. A fivefold increase in whole-body mercury accumulation by rainbow trout ( Oncorhynchus mykiss ) following a fire in Alberta, Canada, apparently resulted from increased nutrient concentrations that enhanced productivity and restructured the food web of a lake within the fire’s burn footprint (Kelly and others, 2006). For this study, we determined the short-term effects of forest fire on mercury concentrations in terrestrial and aquatic environments in VNP by comparing and contrasting mercury concentrations in forest soils, lake waters, and age-1 yellow perch for a burned watershed and an adjacent lake, with similar samples from watersheds and lakes with no fire activity (control watersheds and lakes). The concentration of total mercury in whole, 1-year-old yellow perch serves as a good biological indicator for monitoring trends in methylmercury concentrations in food webs of lakes in North America (Wiener and others, 2007). With a limited gape, age-1 yellow perch that hatched the previous year and resided in a lake for 1 year feed largely on zooplankton and small benthic invertebrates. Thus, age-1 yellow perch provide a baseline for methylmercury concentrations for individual lakes that can be compared across spatial areas. The nine appendixes that accompany this report contain the complete datasets for soils, lake waters, and age-1 yellow perch collected for this study. This report uses data from these three media to provide a framework for evaluating short-term effects of fire on mercury in forested soils and possible effects of the mobilization of mercury from soils on lake water quality and aquatic health.

Minnesota↗

USGS2023

Application of surrogate technology to predict real-time metallic-contaminant concentrations and loads in the Clark Fork near Grant-Kohrs Ranch National Historic Site, Montana, water years 2019–20

Grant-Kohrs Ranch National Historic Site (GRKO) in southwestern Montana commemorates the frontier cattle era and its formative role in shaping the culture and history of the Western United States. The ranch was designated a national historic landmark in 1960 and a unit of the National Park Service (NPS) by Congress in 1972. The GRKO is unique because of its proximity to large-scale extraction, milling, and smelting of gold, silver, copper, and lead ore from the 1860s to the 1980s in the Butte mining district. During this time, mining and milling wastes were discarded in the upper Clark Fork Basin, resulting in the deposition of large amounts of waste materials (tailings) enriched with metallic contaminants (including cadmium, copper, iron, lead, manganese, zinc, and the metalloid trace element arsenic) in soils and in nearby streams and floodplains. Denuded vegetation and fish kills attributed to large concentrations of heavy metals caused the U.S. Environmental Protection Agency to designate a 120-mile section of the Clark Fork River (hereafter referred to as the “Clark Fork”), including GRKO, to be included on the National Priority List for Superfund cleanup in 1989. In 2018, with oversight from the Montana Department of Environmental Quality, the NPS began remediation of 2.6 miles of the Clark Fork as it flows through GRKO property. In 2019, the U.S. Geological Survey (USGS), in collaboration with the NPS, conducted a study using time-series data from backscatter signals from fixed-point turbidity and acoustic sensors with the intent to provide a high-resolution monitoring tool to estimate metallic-contaminant concentrations (MCCs) and loads during NPS remediation of the Clark Fork. Two monitoring sites at USGS streamgages on the Clark Fork on either side of GRKO property were instrumented with turbidity and acoustic sensors and surrogate relations were developed among time-series data and MCCs. The application of high-resolution surrogate data was used to infer contaminant source and fate and evaluate MCC values relative to aquatic-life standards. Using high-resolution surrogate data, it was determined that during spring runoff and storm-related runoff events, MCCs peaked at their highest values at streamflows markedly lower and prior to peak streamflow. Because MCCs peaked prior to streamflow peaks, it could be inferred that the source of MCCs originated from channel bed sediments in close spatial proximity to the monitoring site or from nearby streambanks and floodplains. High-resolution surrogate data revealed that copper concentrations in the Clark Fork exceeded chronic aquatic-life standards 90 percent of the time when streamflow exceeded 200 cubic feet per second (ft 3 /s) and exceeded acute aquatic-life standards 85 percent of the time when streamflow exceeded 260 ft 3 /s. These data helped support NPS management goals for evaluating variation in water quality during remediation of GRKO property, evaluating MCC values relative to aquatic-life standards, and quantifying benefits from Superfund remediation activities.

Montana↗

USGS2005

Geologic and geophysical maps of the Las Vegas 30' x 60' quadrangle, Clark and Nye counties, Nevada, and Inyo County, California

Las Vegas and Pahrump are two of the fastest growing cities in the US, and the shortage of water looms as among the greatest future problems for these cities. These new maps of the Las Vegas 30 x 60-minute quadrangle provide a geologic and geophysical framework and fundamental earth science database needed to address societal issues such as ground water supply and contamination, surface flood, landslide, and seismic hazards, and soil properties and their changing impact by and on urbanization. The mountain ranges surrounding Las Vegas and Pahrump consist of Mesozoic, Paleozoic and Proterozoic rocks. A majority of these rocks are Paleozoic carbonate rocks that are part of Nevada's carbonate rock aquifer province. The Spring Mountains represent a major recharge site in the province, where maximum altitude is 3,632 m (Charleston Peak) above sea level. Rocks in the Sheep and Las Vegas Ranges and Spring Mountains contain correlative, northeast-striking, southeast-verging thrust faults that are part of the Cretaceous, Sevier orogenic belt. These thrusts were offset during the Miocene by the Las Vegas Valley shear system (LVVSZ). We conducted new mapping in the Blue Diamond area, highlighting refined work on the Bird Spring thrust, newly studied ancient landslides, and gravity-slide blocks. We conducted new mapping in the Las Vegas Range and mapped previously unrecognized structures such as the Valley thrust and fold belt; recognition of these structures has led to a refined correlation of Mesozoic thrust faults across the LVVSZ. New contributions in the quadrangle also include a greatly refined stratigraphy of Paleozoic bedrock units based on conodont biostragraphy. We collected over 200 conodont samples in the quadrangle and established stratigraphic reference sections used to correlate units across the major Mesozoic thrust faults. Quaternary deposits cover about half of the map area and underlie most of the present urbanized area. Deposits consist of large coalescing alluvial fans that grade downslope to extensive areas of fine-grained sediment indicative of groundwater-discharge during the Pleistocene. In the central areas of Las Vegas and Pahrump valleys, Quaternary fault scarps associated with past ground-water discharge deposits suggest a genetic relationship. In collaboration with NBMG and University of Nevada, a variety of ages of gravelly alluvium are newly mapped using surficial characteristics and soil development, along with reassessment of previously published mapping during compilation. Reconnaissance geochronology (thermoluminescence and U-series) of eolian and authigenic components of surficial and buried soils and spring deposits is applied to test hypotheses of geomorphic and hydrologic response to climate change over the past 100 k.y.). The major structure in the Las Vegas quadrangle is the LVVSZ. Because the LVVSZ is concealed by thick basin-fill deposits of Quaternary and Tertiary age, it was characterized primarily based on geophysics. Likewise, the newly described State line fault system in Pahrump Valley has also been characterized by geophysics, where geophysically inferred structures correlate remarkably with surface structures defined by our new geologic mapping in the Mound Spring and Hidden Hills Ranch 7.5-minute quadrangles.

Scientific Investigations Map↗

USGS1996

Accumulation of chlorinated benzenes in earthworms

Chlorinated benzenes are widespread in the environment. Hexachlorobenzene, pentachlorobenzene and all isomers of dichlorobenzenes, trichlorobenzenes, and tetrachlorobenzenes, have been detected in fish, water, and sediments from the Great Lakes. This paper describes a long-term (26 week) experiment relating the concentrations of chlorinated benzenes in earthworms to 1) the length of exposure, and it describes three 8-week experiments relating concentrations of chlorinated benzenes in earthworms to 2) their concentration in soil 3) the soil organic matter content and, 4) the degree of chlorination. In the 26-week experiment, the concentration of 1,2,4 - trichlorobenzene in earthworms fluctuated only slightly about a mean of 0.63 ppm (Fig. 1). Although a statistically significant decrease can be demonstrated over the test (Pearson correlation coefficient, r = -0.62 p < 0.05), the decrease was minor. Hexachlorobenzene in earthworms showed a cyclical trend that coincided with replacement of the media, and a slight but statistically significant tendency to increase from about 2 to 3 ppm over the 26 weeks (r = 0.55, p < 0.05). Concentrations of both trichlorobenzene and hexachlorobenzene in earthworms increased as the concentrations in the soil increased (Fig. 2), but leveled off at the highest soil concentrations. The most surprising result of this study was the relatively low concentrations in earthworms compared to those in soils. The average concentration of each of the six isomers of trichlorobenzene and tetrachlorobenzene in earthworms was only about 1 ppm (Table 2); the isomeric structure did not affect accumulation. The concentration of organic matter in soil had a prominent effect on hexachlorobenzene concentrations in earthworms (Fig. 3). Hexachlorobenzene concentrations decreased steadily from 9.3 ppm in earthworms kept in soil without any peat moss added to about 1 ppm in soil containing 16 or 32% organic matter.

Bulletin of Environmental Contamination and Toxico↗

USGS2010

Assessing the vulnerability of public-supply wells to contamination: Glacial aquifer system in Woodbury, Connecticut

This fact sheet highlights findings from the vulnerability study of a public-supply well in Woodbury, Connecticut. The well typically produces water at the rate of 72 gallons per minute from the glacial aquifer system in the Pomperaug River Basin. Water samples were collected at the public-supply well and at monitoring wells installed in or near the simulated zone of contribution to the supply well. Samples of untreated water from the public-supply wellhead contained several types of undesirable constituents, including 11 volatile organic compounds (VOCs), nitrate, pesticides, uranium, and radon. Most of these constituents were detected at concentrations below drinking-water standards, where such standards exist. Only concentrations of the VOC trichlorethylene exceeded the Maximum Contaminant Level (MCL) of 5 micrograms per liter (ug/L) established by U.S. Environmental Protection Agency for drinking water. Radon concentrations exceeded a proposed-but not finalized-MCL of 300 picocuries per liter (pCi/L). Overall, the study findings point to four main factors that affect the movement and fate of contaminants and the vulnerability of the public-supply well in Woodbury: (1) groundwater age (how long ago water entered, or recharged, the aquifer); (2) the percentage of recharge received through urban areas; (3) the percentage of recharge received through dry wells and their proximity to the public-supply well; and (4) natural geochemical processes occurring within the aquifer system; that is, processes that affect the amounts and distribution of chemical substances in aquifer sediments and groundwater. A computer-model simulation of groundwater flow to the public-supply well was used to estimate the age of water particles entering the well along the length of the well screen. About 90 percent of the simulated flow to the well consists of water that entered the aquifer 9 or fewer years ago. Such young water is vulnerable to contaminants resulting from human activities, as indicated by the solvents, fuel components, road salt, and septic-system leachate that were detected in the glacial aquifer system during the current study. Age-dating combined with chemical modeling suggests that less than 2 percent of water produced by the public-supply well is water from the deep bedrock that is "old" (water that recharged, or entered, the aquifer before 1952). Such a small percentage of old groundwater entering the public-supply well offers little potential for dilution of young waters containing contaminants from human activities. Shallow groundwater that originated as recharge through urban areas generally had higher median concentrations and more detections of volatile organic compounds (VOCs) than did groundwater from the deep glacial deposits or fractured bedrock that originated mainly as recharge through agricultural and undeveloped land. Shallow groundwater was also found to be affected by road salt and septic-system leachate. A chemical mixing model indicates that up to 15 percent of nitrate in water from the supply well is likely from septic-system leachate. The Connecticut Department of Public Health has identified several potential sources of contamination in the commercial area of Woodbury (several light industrial or commercial properties where hazardous materials and petroleum products are used and stored). To reduce stormwater runoff in the commercial area, water from the parking lots and pavement is channeled into dry wells-drains that shunt water directly into the aquifer system, bypassing the soil and unsaturated zones. A computer-model simulation of groundwater flow indicates that approximately 16 percent of the water produced by the public-supply well is derived from runoff captured by these drains. Traveltime for water from the dry wells to the public-supply well ranges from about 1.5 to less than 4 years. Dry wells have the potential to enhance contaminant movement to the supply well, suggesting that stormwater-control methods cannot be considered separately from groundwater quality—they are linked. Water-quality protection in this setting depends on the entire community. If residents and businesses take steps to reduce input of manmade contaminants to groundwater, a positive effect on quality of the supply-well water might begin to be seen in less than 10 years, owing to the short residence time of water in the aquifer.

Connecticut↗

USGS1998

Nitrate and pesticides in ground water in the eastern San Joaquin Valley, California : Occurrence and trends

The occurrence of nitrate and pesticides in ground water in California's eastern San Joaquin Valley may be greatly influenced by the long history of intensive farming and irrigation and the generally permeable sediments. This study, which is part of the U.S. Geological Survey National Water-Quality Assessment Program, was done to assess the quality of the ground water and to do a preliminary evaluation of the temporal trends in nitrate and pesticides in the alluvial fans of the eastern San Joaquin Valley. Ground-water samples were collected from 30 domestic wells in 1995 (each well was sampled once during 1995). The results of the analyses of these samples were related to various physical and chemical factors in an attempt to understand the processes that control the occurrence and the concentrations of nitrate and pesticides. A preliminary evaluation of the temporal trends in the occurrence and the concentration of nitrate and pesticides was done by comparing the results of the analyses of the 1995 ground-water samples with the results of the analyses of the samples collected in 1986-87 as part of the U.S. Geological Survey Regional Aquifer-System Analysis Program. Nitrate concentrations (dissolved nitrate plus nitrite, as nitrogen) in ground water sampled in 1995 ranged from less than 0.05 to 34 milligrams per liter, with a median concentration of 4.6 milligrams per liter. Nitrate concentrations exceeded the maximum contaminant level of 10 milligrams per liter (as nitrogen) in 5 of the 30 ground-water samples (17 percent), whereas 12 of the 30 samples (40 percent) had nitrate concentrations less than 3.0 milligrams per liter. The high nitrate concentrations were associated with recently recharged, well-oxygenated ground water that has been affected by agriculture (indicated by the positive correlations between nitrate, dissolved-oxygen, tritium, and specific conductance). Twelve pesticides were detected in 21 of the 30 ground-water samples (70 percent) in 1995, although only 5 pesticides were detected in more than 10 percent of the ground-water samples. All 12 pesticides were detected at concentrations below the maximum contaminant levels, except the banned soil fumigants 1,2-dibromo-3-chloropropane (3 detections) and 1,2-dibromoethane (1 detection). Atrazine and desethyl atrazine (a transformation product of atrazine) were the most frequently detected pesticides; they were detected in 11 ground-water samples. The frequent detections of atrazine and desethyl atrazine may be related either to past applications of atrazine or to recent application on rights-of-way. Simazine was detected in 10 ground-water samples and diuron was detected in 4 ground-water samples. The detections of simazine and diuron are generally consistent with their reported applications on the crops near the wells where they were detected. 1,2,3-trichloropropane, a manufacturing by-product of 1,2-dichloropropane and 1,3- dichloropropene formulations, was detected in 4 ground-water samples. The occurrence of 1,2,3-trichloropropane, 1,2-dibromo-3-chloropropane, and 1,2-dibromoethane is probably related to past use. Similar to nitrate concentrations, pesticide occurrence was positively correlated to dissolved-oxygen concentrations, indicating that areas with high dissolved-oxygen concentrations may be vulnerable to contamination by nitrate and pesticides. High dissolved-oxygen concentrations may be associated with water that has been rapidly recharged. A comparison of the concentrations and the occurrence of nitrate and pesticides between 1986-87 and 1995 indicates that nitrate concentrations may pose a greater threat to the quality of the ground-water resource in this region than pesticides, in the context of current drinking-water standards. Nitrate concentrations were significantly higher in the 1995 ground-water samples than in the 1986-87 samples collected from the same wells.

Calfornia↗

USGS2011

Review of samples of water, sediment, tailings, and biota at the Little Bonanza mercury mine, San Luis Obispo County, California

Background and Objectives The Little Bonanza mercury (Hg) mine, located in San Luis Obispo County, California, is a relatively small mine with, a historical total Hg production of about 1,000 flasks. The mine workings and tailings are located in the headwaters of the previously unnamed west fork of Las Tablas Creek (WF Las Tablas Creek), which flows into the Nacimiento Reservoir. Wasterock and tailings eroded from the Little Bonanza Hg Mine have contributed Hg-enriched mine wastes to the headwaters of WF Las Tablas Creek. The mine is located on Federal land managed by the U.S. Bureau of Land Management (BLM), which requested that the U.S. Geological Survey (USGS) measure and characterize Hg and other geochemical constituents in tailings, sediment, water, and biota at and downstream from the minesite. This report is in response that request, from the lead agency which is mandated to conduct a Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) - Removal Site Investigation (RSI). The RSI applies to removal of Hg-contaminated mine waste from the Little Bonanza minesite as a means of reducing Hg transport to WF Las Tablas Creek. This report summarizes data obtained from field sampling of mine tailings, wasterock, sediment, water, and biota at the Little Bonanza Mine that was completed on April 6, 2010. Conditions during sampling were dry and no rain had occurred in the watershed for several weeks. Our results permit a preliminary assessment of the mining sources of Hg and associated chemical constituents that could produce elevated levels of monomethyl mercury (MMeHg) in WF Las Tablas Creek and in biota. History and Geology The history of the Little Bonanza Hg mine is summarized here from Yates (1943) and other references as cited. The Little Bonanza Mine, located 20 mi west of Paso Robles, was discovered in 1862. Although production was minor until 1900, from 1900 to 1906, the mine produced about 1,000 flasks of Hg. Intermittent production continued into the 1940s but was relatively limited. Underground workings, now caved and inaccessible, include about 3,000 ft of drifts, crosscuts, and raises on three levels extending 260 ft downward. The workings at the Little Bonanza Mine explore a zone of fault breccia, which trends northwest. The breccia is composed of fragments of sandstone, greenstone, serpentine, and chert in a shale matrix. The serpentine has been hydrothermally altered to silica-carbonate rock, and the Hg deposit is hosted within the zone of alteration. The veins are discontinuous and irregular, but form a steplike pattern along the fault zone. The principal mineralization occurring in the veins is irregular, consisting of disseminated zones of cinnabar. Most of the veins in the mine area contain cinnabar. Sample Sites and Methods Samples were collected to assess the concentrations of Hg and biogeochemically relevant constituents in tailings and wasterock piles at the Little Bonanza Hg mine. Tailings are present adjacent to a three-pipe retort used to process the Hg ore. The tailings occur in the upper 15 cm of the soil adjacent to the retort and slag from the retort is present on the surface. An area of disturbed soil and rock uphill from the retort was likely formed during construction of a dam that provided water for mining activities. Wasterock in these piles was sampled. The largest amount of tailings is exposed to the west of the retort in the bank of WF Las Tablas Creek. Water, sediment, and biota were sampled from WF Las Tablas Creek, which flows through the mine area. Sample-site locations are shown in figures 10 and 11 and listed in table 1. Samples were collected when streamflow was low and no precipitation had occurred.

California↗

USGS2002

Mercury loading and methylmercury production and cycling in high-altitude lakes from the Western United States

Studies worldwide have shown that mercury (Hg) is a ubiquitous contaminant, reaching even the most remote environments such as high-altitude lakes via atmospheric pathways. However, very few studies have been conducted to assess Hg contamination levels of these systems. We sampled 90 mid-latitude, high-altitude lakes from seven national parks in the western United States during a four-week period in September 1999. In addition to the synoptic survey, routine monitoring and experimental studies were conducted at one of the lakes (Mills Lake) to quantify MeHg fluxrates and important process rates such as photo-demethylation. Results show that overall, high-altitude lakes have low total mercury (HgT) and methylmercury (MeHg) levels (1.07 and 0.05 ng L -1 , respectively), but a very good correlation of Hg to MeHg (r 2 = 0.82) suggests inorganic Hg(II) loading is a primary controlling factor of MeHg levels in dilute mountain lakes. Positive correlations were also observed for dissolved organic carbon (DOC) and both Hg and MeHg, although to a much lesser degree. Levels of MeHg were similar among the seven national parks, with the exception of Glacier National Park where lowerconcentrations were observed (0.02 ng L -1 ), and appear to be related to naturally elevated pH values there. Measured rates ofMeHg photo-degradation at Mills Lake were quite fast, and this process was of equal importance to sedimentation and stream flow for removing MeHg. Enhanced rates of photo-demethylation are likely an important reason why high-altitude lakes, with typically high water clarity and sunlight exposure, are low in MeHg.

California, Colorado, Montana, Wyoming↗

USGS2010

Rate of formation and dissolution of mercury sulfide nanoparticles: The dual role of natural organic matter

Mercury is a global contaminant of concern due to its transformation by microorganisms to form methylmercury, a toxic species that accumulates in biological tissues. The effect of dissolved organic matter (DOM) isolated from natural waters on reactions between mercury(II) (Hg) and sulfide (S(-II)) to form HgS (s) nanoparticles across a range of Hg and S(-II) concentrations was investigated. Hg was equilibrated with DOM, after which S(-II) was added. Dissolved Hg (Hg aq ) was periodically quantified using ultracentrifugation and chemical analysis following the addition of S(-II). Particle size and identity were determined using dynamic light scattering and X-ray absorption spectroscopy. S(-II) reacts with Hg to form 20 to 200nm aggregates consisting of 1-2 nm HgS (s) subunits that are more structurally disordered than metacinnabar in the presence of 2 x 10 -9 to 8 x 10 -6 M Hg and 10 (mg C)L -1 DOM. Some of the HgS(s) nanoparticle aggregates are subsequently dissolved by DOM and (re)precipitated by S(-II) over periods of hours to days. At least three fractions of Hg-DOM species were observed with respect to reactivity toward S(-II): 0.3 μmol reactive Hg per mmol C (60 percent), 0.1 μmol per mmol C (20 percent) that are kinetically hindered, and another 0.1 μmol Hg per mmol C (20 percent) that are inert to reaction with S(-II). Following an initial S(-II)-driven precipitation of HgS (s) , HgS (s) was dissolved by DOM or organic sulfur compounds. HgS (s) formation during this second phase was counterintuitively favored by lower S(-II) concentrations, suggesting surface association of DOM moieties that are less capable of dissolving HgS (s) . DOM partially inhibits HgS(s) formation and mediates reactions between Hg and S(-II) such that HgS (s) is susceptible to dissolution. These findings indicate that Hg accessibility to microorganisms could be controlled by kinetic (intermediate) species in the presence of S(-II) and DOM, undermining the premise that equilibrium Hg species distributions should correlate to the extent or rate of Hg methylation in soils and sediments.

Geochimica et Cosmochimica Acta↗

USGS2010

Combined use of groundwater dating, chemical, and isotopic analyses to resolve the history and fate of nitrate contamination in two agricultural watersheds, Atlantic coastal plain, Maryland

The history and fate of groundwater nitrate (NO 3 − ) contamination were compared in 2 small adjacent agricultural watersheds in the Atlantic coastal plain by combined use of chronologic (CCl 2 F 2 , 3 H), chemical (dissolved solids, gases), and isotopic (δ 15 N,δ 13 C, δ 34 S) analyses of recharging groundwaters, discharging groundwaters, and surface waters. The results demonstrate the interactive effects of changing agricultural practices, groundwater residence times, and local geologic features on the transfer of NO 3 − through local flow systems. Recharge dates of groundwaters taken in 1990–1992 from the surficial aquifer in the Chesterville Branch and Morgan Creek watersheds near Locust Grove, Maryland, ranged from pre-1940 to the late 1980’s. When corrected for localized denitrification by use of dissolved gas concentrations, the dated waters provide a 40-year record of the recharge rate of NO 3 − , which increased in both watersheds by a factor of 3–6, most rapidly in the 1970's. The increase in groundwater NO 3 − over time was approximately proportional to the documented increase in regional N fertilizer use, and could be accounted for by oxidation and leaching of about 20–35% of the fertilizer N. Groundwaters discharging upward beneath streams in both watersheds had measured recharge dates from pre-1940 to 1975, while chemical data for second-order reaches of the streams indicated average groundwater residence times in the order of 20+ years. At the time of the study, NO 3 − discharge rates were less than NO 3 − recharge rates for at least two reasons: (1) discharge of relatively old waters with low initial NO 3 − concentrations, and (2) local denitrification. In the Chesterville Branch watershed, groundwaters remained oxic throughout much of the surficial aquifer and discharged relatively unaltered to the stream, which had a relatively high NO 3 − concentration (9–10 mg/L as N). In the Morgan Creek watershed, groundwaters were largely reduced and denitrified before discharging to the stream, which had a relatively low NO 3 − concentration (2–3 mg/L as N). Chemical and isotopic data indicate that quantitative denitrification occurred within buried calcareous glauconitic marine sediments that are present at relatively shallow depths beneath the Morgan Creek watershed. NO 3 − removal by forests, wetlands, and shallow organic-rich soils in near-stream environments was largely avoided by groundwaters that followed relatively deep flow paths before converging and discharging rapidly upward to the streams.

Maryland↗

USGS1999

Surface-water-quality assessment of the Yakima River basin, Washington: Overview of major findings, 1987-91

Surface-water-quality conditions were assessed in the Yakima River Basin, which drains 6,155 square miles of mostly forested, range, and agricultural land in Washington. The Yakima River Basin is one of the most intensively farmed and irrigated areas in the United States, and is often referred to as the “Nation’s Fruitbowl.” Natural and anthropogenic sources of contaminants and flow regulation control water-quality conditions throughout the basin. This report summarizes the spatial and temporal distribution, sources, and implications of the dissolved oxygen, water temperature, pH, suspended sediment, nutrient, organic compound (pesticide), trace element, fecal indicator bacteria, radionuclide, and aquatic ecology data collected during the 1987–91 water years. The Yakima River descends from a water surface altitude of 2,449 feet at the foot of Keechelus Dam to 340 feet at its mouth downstream from Horn Rapids Dam near Richland. The basin can be divided into three distinct river reaches on the basis of its physical characteristics. The upper reach, which drains the Kittitas Valley, has a high gradient, with an average streambed slope of 14 feet per mile (ft/mi) over the 74 miles from the foot of Keechelus Dam (river mile [RM] 214.5) to just upstream from Umtanum. The middle reach, which drains the Mid Valley, extends a distance of 33 miles from Umtanum (RM 140.4) to just upstream from Union Gap and also has a high gradient, with an average streambed slope of 11 ft/mi. The lower reach of the Yakima River drains the Lower Valley and has an average streambed slope of 7 ft/mi over the 107 miles from Union Gap (RM 107.2) to the mouth of the Yakima River. These reaches exhibited differences in water-quality conditions related to the differences in geologic sources of contaminants and land use. Compared with the rest of the basin, the Kittitas Valley and headwaters of the Naches River Subbasin had relatively low concentrations and loads of suspended sediment, nutrients, organic compounds, and fecal indicator bacteria. There were very few failures to meet the Washington State dissolved oxygen standard or exceedances of the water temperature and pH standards in this reach. In general, these areas are considered to be areas of lessdegraded water quality in the basin. The preTertiary metamorphic and intrusive rocks of the Cle Elum and Teanaway River Subbasins, however, were found to be significant geologic sources of antimony, arsenic, chromium, copper, mercury, nickel, selenium, and zinc. As a result, the arsenic, chromium, and nickel concentrations measured in the streambed sediment of the Kittitas Valley were 13 to 74 times higher than those measured in the Lower Valley. The Mid and Lower Valleys had similar water-quality conditions, governed by the intensive agricultural and irrigation activities, highly erosive landscapes, and flow regulation. Most of the failures to meet the Washington State standards for dissolved oxygen and exceedances of the standards for water temperature and pH occurred in the Mid and Lower Valleys. Agricultural drains in the Mid and Lower Valleys were found to be significant sources of nutrients, suspended sediment, pesticides, and fecal indicator bacteria. Downstream from the irrigation diversions near Union Gap, summertime streamflow in the Yakima River was drastically reduced to only a few hundred cubic feet per second. In the lower Yakima River, agricultural return flow typically accounts for as much as 80 percent of the main stem summertime flow near the downstream terminus of the basin. Therefore, the water-quality characteristics of the lower Yakima River resemble those of the agricultural drains. The highest fecal bacteria concentrations (35,000 colonies of Escherichia coli per 100 milliliters of water) were measured in the Granger/Sunnyside area, the location of most of the livestock in the basin. The east side area of the Lower Valley (area east of the Yakima River) was the predominant source area for suspended sediment and pesticides in the basin. This area had the largest acreage of irrigated land and generally received the largest application of pesticides. Owing to the highly erosive soils of the area, the suspended sediment load from the east side in June 1989 (320 kilograms per day) was five or more times larger than from any other area, and the loads of several of the more hydrophobic organic compounds were four or more times larger. An ecological assessment of the Yakima River Basin ranked physical, chemical, and biological conditions at impaired (degraded) sites against reference sites in an effort to understand how land use changes physical and chemical site characteristics and how biota respond to these changes. For this assessment, the basin was divided into four natural ecological categories: (1) Cascades ecoregion, (2) Eastern Cascades Slopes and Foothills ecoregion, (3) Columbia Basin ecoregion, and (4) large rivers. Each of these categories has a unique combination of climate and landscape features that produces a distinctive terrestrial vegetation assemblage. In the combined Cascades and Eastern Cascades site group, which had the fewest impaired sites, the metals index was the only physical and chemical index that indicated any impairment. The moderate levels of impairment noted in the invertebrate and algal communities were not, however, associated with metals, and may have been related to the effects of logging, although the intensity of logging was not directly quantified in this study. Sites in the Columbia Basin site group were all moderately or severely impaired with the exception of the two reference sites (Umtanum Creek and Satus Creek below Dry Creek), which showed no physical, chemical, or biological impairment. Three sites were heavily affected by agriculture (Granger Drain, Moxee Drain, and Spring Creek) and were listed as severely impaired by most of the physical, chemical, and biological condition indices. Agriculture was the primary cause of the impairment of biological communities in this site group. The primary physical and chemical indicators of agricultural effects were nutrients, pesticides, dissolved solids, and substrate embeddedness, which all tended to increase with agricultural intensity. The biological effects of agriculture were manifested by a decrease in the abundance and number of native species of fish and invertebrates, a shift in algal communities to species indicative of eutrophic conditions, and higher abundances. There was also an increase in the abundance and number of nonnative fish species due to the prevalence of fish that are largely tolerant of nutrient-rich conditions. Main stem (large river) sites downstream from the city of Yakima exhibited severe impairment of fish communities associated with high levels of pesticides in fish tissues and the presence of external anomalies on fish.

Washington↗

USGS2017

Multiple-source tracking: Investigating sources of pathogens, nutrients, and sediment in the Upper Little River Basin, Kentucky, water years 2013–14

The South Fork Little River (SFLR) and the North Fork Little River (NFLR) are two major headwater tributaries that flow into the Little River just south of Hopkinsville, Kentucky. Both tributaries are included in those water bodies in Kentucky and across the Nation that have been reported with declining water quality. Each tributary has been listed by the Kentucky Energy and Environment Cabinet—Kentucky Division of Water in the 303(d) List of Waters for Kentucky Report to Congress as impaired by nutrients, pathogens, and sediment for contact recreation from point and nonpoint sources since 2002. In 2009, the Kentucky Energy and Environment Cabinet—Kentucky Division of Water developed a pathogen total maximum daily load (TMDL) for the Little River Basin including the SFLR and NFLR Basins. Future nutrient and suspended-sediment TMDLs are planned once nutrient criteria and suspended-sediment protocols have been developed for Kentucky. In this study, different approaches were used to identify potential sources of fecal-indicator bacteria (FIB), nitrate, and suspended sediment; to inform the TMDL process; and to aid in the implementation of effective watershed-management activities. The main focus of source identification was in the SFLR Basin. To begin understanding the potential sources of fecal contamination, samples were collected at 19 sites for densities of FIB ( E. coli ) in water and fluvial sediment and at 11 sites for Bacteroidales genetic markers (General AllBac, human HF183, ruminant BoBac, canid BacCan, and waterfowl GFD) during the recreational season (May through October) in 2013 and 2014. Results indicated 34 percent of all E. coli water samples ( n =227 samples) did not meet the U.S. Environmental Protection Agency 2012 recommended national criteria for primary recreational waters. No criterion currently exists for E. coli in fluvial sediment. By use of the Spearman’s rank correlation test, densities of FIB in fluvial sediments were observed to have a statistically significant positive correlation with drainage area. As drainage area increased, so did the densities of FIB in the fluvial sediments. There was no statistically significant correlation between drainage area and FIB in water. The human-associated marker (HF183) was found above the detection limit in 26 percent of the samples ( n =120 samples); a higher proportion of positive samples was in the NFLR Basin. The ruminant-associated marker (BoBac) was above the detection limit in 65 percent of samples; a higher proportion of positive samples was in the headwaters of the SFLR Basin. Nutrient yields differed between the SFLR and NFLR Basins. Comparatively, the SFLR Basin produced the largest estimated mean yields of total nitrogen (16,000 pounds per year per square mile (lb/yr/mi 2 ) and nitrite plus nitrate nitrogen (12,500 lb/yr/mi 2 ), and the NFLR Basin produced the largest estimated mean yields of ammonia plus organic nitrogen (4,700 lb/yr/mi 2 ), total phosphorus (1,100 lb/yr/mi 2 ), and orthophosphorus (590 lb/yr/mi 2 ). Nitrate sources in surface water were assessed in both basins using dual-nitrate isotope (nitrogen and oxygen) ratios. Data from the different land uses in the SFLR Basin showed differences in nitrate concentrations and overlapping, but moderately distinct, isotopic signatures. Predominantly forested sites consistently had low nitrate concentrations (median = 0.233 milligrams per liter) with minimal variability, and agricultural sites had the highest nitrate concentrations (median = 7.55 milligrams per liter) with the greatest variability. The median nitrate concentration for sites with mixed land use was 2.66 milligrams per liter. Dual-isotope data for forested sites plotted within ranges characteristic of soil-derived nitrate with possible but minimal influence from recycled atmospheric nitrate. Ranges of dual-isotope data for sites with agricultural and mixed land uses were characteristic of possible mixtures of chemical fertilizer, soil-derived nitrate, and manure and septic wastes. In the NFLR Basin, a positive linear relation was observed between nitrate concentrations and nitrogen isotope ratios (δ 15 N NO3 ) (R 2 =0.56; p -value <0.001) that potentially suggests the NFLR Basin has a higher proportion of δ 15 N NO3 -enriched sources, such as manure and sewage. However, mixing of other nitrate-derived sources cannot be excluded, because many values of δ 15 N NO3 and concentrations of nitrate showed minimal variation and plotted within dual-nitrate isotope ranges characteristic of fertilizer and soil-derived nitrate sources. A sediment-fingerprinting approach was used to quantify the relative contribution of four upland sources in the SFLR Basin (agricultural, pasture, riparian/forest, and streambank) to understand how land management affects suspended-sediment concentration. Carbon isotope ratios (δ 13 C), together with calcium and carbon concentrations, were the best indicators of sediment source; the uncertainty was less than 11 percent. Fine-sediment samples collected at the SFLR Basin outlet indicated streambanks as the largest source of the fine sediment to the stream followed by cropland and riparian/forest-source areas, respectively; pasture was a minor contributing source. Streambanks and cropland were essentially equal contributors of fine sediment at the NFLR Basin outlet.

Kentucky↗

USGS2022

Mapping areas of groundwater susceptible to transient contamination events from rapid infiltration into shallow fractured-rock aquifers in agricultural regions of the conterminous United States

Current time-invariant groundwater vulnerability assessments may not capture intermittent contamination events in landscape areas that experience rapid infiltration following precipitation or snowmelt. Occurrences of rapid infiltration and intermittent degradation of groundwater quality are frequently reported in fractured-rock aquifers. This investigation identifies landscape areas underlain by fractured rock within the conterminous United States (CONUS) that may be susceptible to rapid infiltration and where groundwater is a principal source of water supply to the population. Our analysis shows that approximately 27 percent of the CONUS, corresponding to a population of approximately 150 million people, is both underlain by fractured rock and denoted as an area of significant groundwater use. The results of this survey identified shallow fractured-rock aquifers underlying glacial sediments in the upper Midwest and northeastern United States as areas that may be subject to rapid infiltration events. Additionally, aquifers associated with the early Mesozoic basins located in the northeastern and mid-Atlantic United States and bands of carbonate aquifers in the southeastern United States show high susceptibility to rapid infiltration. Index values used in this investigation indicate isolated areas in the western half of the United States also show high susceptibility to rapid infiltration. The isolated areas in Oklahoma, Texas, Arkansas, and southwestern Missouri correspond to karst regions of carbonate aquifers. The isolated areas showing high susceptibility to rapid infiltration and contamination from agricultural sources are locations where more detailed investigations of transient contamination events are warranted. This survey also addresses the potential for contaminant longevity in fractured-rock aquifers stemming from intermittent contamination events. Contaminants that can dissolve into the groundwater following infiltration may be introduced into fractures, and the dissolved constituents can diffuse from fractures into the porosity of the adjacent rock matrix. These constituents can then diffuse back into permeable fractures and adversely affect groundwater quality at downgradient locations over an extended time frame. Rock types with larger matrix porosities have the capacity to retain and then release larger quantities of dissolved constituents, resulting in longer residence times for dissolved groundwater contaminants. The magnitude of the dissolved contaminant concentration infiltrating to the water table will also dictate whether the contaminant concentration in the groundwater exceeds limits for human consumption over the duration of a contamination event. In general, sedimentary- and carbonate-rock aquifers have larger matrix porosities in comparison to igneous- and metamorphic-rock aquifers, and thus, they are more susceptible to longer contaminant residence times. Aquifers composed of sedimentary or carbonate rock constitute approximately 51 percent of the CONUS, and 19 percent of the CONUS is associated with sedimentary- or carbonate-rock aquifers that are of significance for groundwater use. Depending on the contaminants of concern and the concentration of the contaminants introduced into the groundwater from infiltrating water, it would be beneficial for investigations of susceptibility to rapid infiltration to also consider the potential for contaminant longevity. This investigation identifies areas of rapid infiltration into fractured rock using index values applied to the attributes (1) depth to the water table, (2) depth to bedrock, and (3) percentage of sand in soil, where larger index values indicate a greater susceptibility to rapid infiltration. These attributes are selected as the most likely factors that affect rapid infiltration to the water table. The combination of depth to water table and depth to bedrock highlight those aquifer settings that are characterized as shallow fractured-rock aquifers, where the water table may reside either in the bedrock or in overlying unconsolidated geologic materials. In addition, we consider the percentage of agricultural use as a land-use attribute when formulating an index of susceptibility to rapid infiltration and contamination. Agricultural areas are well recognized as nonpoint sources of contaminants that can affect groundwater quality because of seasonal amendments applied to the land surface. Rural agricultural areas are also characterized by septic tanks and leach fields for onsite treatment of wastewater, which may also be a source of contamination that may be introduced into the groundwater following precipitation or snowmelt events.

Conterminous United States↗

USGS1996

Geology, hydrogeology, and potential of intrinsic bioremediation at the National Park Service Dockside II site and adjacent areas, Charleston, South Carolina, 1993-94

A long history of industrial and commercial use of the National Park Service property and adjacent properties located in downtown Charleston, South Carolina, has caused extensive contamination of the shallow subsurface soils and water-table aquifer. The National Park Service property is located adjacent to a former manufactured-gas plant site, which is the major source of the contamination. Contamination of this shallow water-table aquifer is of concern because shallow ground water discharges to the Cooper River and contains contaminants, which may affect adjacent wildlife or human populations. The geology of the National Park Service property above the Ashley Formation of the Cooper Group consists of two Quaternary lithostratigraphic marine units, the Wando Formation and Holocene deposits, overlain by artificial fill. The Wando Formation overlies the Ashley Formation, a sandy calcareous clay, and consists of soft, organic clay overlain by gray sand. The Holocene deposits are composed of clayey to silty sand and soft organic-rich clay. The artificial fill, which was placed at the site to create dry land where salt marsh existed previously, is composed of sand, silt, and various scrap materials. The shallow hydrogeology of the National Park Service property overlying the Ashley Formation can be subdivided into two sandy aquifers separated by a leaky, black, organic-rich clay. The unconfined upper surficial aquifer is primarily artificial fill. The lower surficial aquifer consists of the Wando sand unit and is confined by the leaky organic-rich clay. Aquifer tests performed on the wells screened in these aquifers resulted in hydraulic conductivities from 0.1 to 10 feet per day for the upper surficial aquifer, and 16 feet per day for the lower surficial aquifer. Vertical hydraulic gradients at the site are typically low. A downward gradient from the upper surficial aquifer to the lower surficial aquifer occurs throughout most of the year. A brick-lined storm-water-drainage archway located in the study area is a conduit for the overflow of seawater into the surficial aquifer during exceptionally high tides. The efficiency of intrinsic bioremediation to reduce contaminant migration in the upper surficial aquifer at the National Park Service site was assessed to determine if, and at what concentrations, contaminants are being transported to the Cooper River. This assessment required incorporating hydrologic, geochemical, microbiologic, and demographic information into a predictive solute-transport model to determine rates of contaminant transport to the Cooper River. The transport of toluene and naphthalene was modeled as a surrogate for the transport of aromatic and other hydrocarbon compounds at the study area. Laboratory estimates of the adsorption coefficients for sediments of the upper surficial aquifer suggest preferential adsorption of naphthalene over toluene. The adsorption coefficient of naphthalene is at least two orders of magnitude greater than that determined for toluene. Laboratory microbial-biodegradation experiments indicate that microorganisms present in the shallow aquifer have the potential to degrade toluene under anaerobic and aerobic conditions, and naphthalene primarily under aerobic conditions. Rates of microbial biodegradation are similar for both compounds under aerobic conditions. Flow-model calibration to the January 1994 water-table surface of the upper surficial aquifer was achieved by specifying appropriate hydrogeologic boundary conditions and using hydraulic conductivity values determined in the field. The brick-lined storm-water drainage archway located in the study area was modeled to account for ground-water discharge through this drain. An exploratory modeling approach was used to evaluate the range of possible solutions that approximate the transport of contaminants to the observed distributions. Approximate toluene solute-transport conditions for January 1994 were estimated using velocity dist

South Carolina↗

USGS1998

Water-quality assessment of part of the upper Mississippi River basin, Minnesota and Wisconsin— Ground-water quality in an urban part of the Twin Cities Metropolitan area, Minnesota, 1996

In the spring of 1996, the Upper Mississippi River Basin Study Unit of the National Water-Quality Assessment Program drilled 30 shallow monitoring wells in a study area characterized by urban residential and commercial land uses. The monitoring wells were installed in sandy river-terrace deposits adjacent to the Mississippi River in Anoka and Hennepin Counties, Minnesota, in areas where urban development primarily occurred during the past 30 years. Analyses of sediments collected during well drilling indicated that at most well sites the aquifer materials had relatively high hydraulic conductivities (ranging from 0.01 to 238 feet per day), and relatively low organic carbon contents (0.10 to 41 grams per kilogram), indicating a high susceptibility to leaching of fertilizers and organic substances used on the land surface. Sediment pH values, which can affect leaching of pesticides, were generally alkaline, ranging from 5.1 to 9.6. Ground-water levels ranged from 2.39 to 23.14 feet below land surface, and indicated that shallow ground water flows primarily toward the Mississippi River. Dissolved-oxygen concentrations in water samples from the wells were generally less than 3 milligrams per liter (mg/L) and specific conductances were generally greater than 600 microsiemens per centimeter. Calcium, magnesium, sodium, bicarbonate, chloride, and sulfate were the primary dissolved constituents in the water samples. Sodium and chloride concentrations were generally greater than commonly reported in the region, probably due to leaching of sodium chloride applied to roads during the winter. Most tracemetal concentrations in ground-water samples were less than 10 micrograms per liter (μg/L), but concentrations of iron and manganese commonly exceeded Secondary Maximum Contaminant Levels set by the U.S. Environmental Protection Agency of 300 and 50 μg/L, respectively. Mineral saturation indices indicated that calcite, dolomite, and gypsum were slightly undersaturated in most water samples, and that quartz, and many oxides and hydroxides of iron and manganese were oversaturated in all of the water samples. Concentrations of nitrate nitrogen, the primary nutrient of concern in ground water, ranged from less than 0.05 to 16 mg/L, with a median concentration of 1.4 mg/L. Dissolved phosphorus concentrations ranged from less than 0.01 to 1.5 mg/L in the water samples, with a median concentration of 0.02 mg/L. Water from one well was oversaturated with respect to hydroxyapatite, a phosphatic mineral used as a fertilizer. Pesticide compounds were detected in water samples from 16 wells, but concentrations of those compounds were less than 1.0 μg/L. Prometon, an herbicide commonly used for right-of-way weed control, was detected in water samples from 10 of the wells. Atrazine, and its metabolite deethylatrazine, were detectable in water samples from 6 and 8 wells, respectively. Atrazine is commonly applied to land planted with corn and is detectable in rainfall and air samples in concentrations of less than 1 ng/L in the urban land use study area. Other detected pesticide compounds, which are used in agriculture, right-of-way weed control, or lawn care included: tebuthiuron, EPTC, p , p '-DDE, metolachlor, simazine, bentazon, and bromacil. Volatile organic compounds were detected in water samples from 26 wells, but the concentrations of most of those compounds were less than 1 μg/L. Carbon disulfide, which may be produced by bacteria in soils, was the most commonly detected volatile organic compound in water samples from the wells. Other detected volatile organic compounds included: methyl chloride, acetone, dichlorofluoromethane, tetrahydrofuran, trichlorofluoromethane, methyl iodide, 1,1-dichloroethane, chloroform, toluene, trichloroethane, trichloroethene, cis -1,2-dichloroethene, methylene chloride, bromodichloromethane, benzene, methylisobutylketone, ethyl ether, and tetrachloroethene. Tritium concentrations, analyzed in water samples from 15 of the 30 wells, indicated that shallow ground water has been recharged since the mid-1950's, and that shallow ground water should be affected by urban development that has taken place over the past 40 years. Land uses in the urban land use study area affected the concentrations of some water-quality constituents. Concentrations of nitrate and chloride, and frequencies of detection of pesticides and of volatile organic compounds, were greater in water samples from the surficial sand and gravel aquifer underlying the urban land use study area than in water samples from similar aquifers from part of the Upper Mississippi River Basin National Water-Quality Assessment study unit. Land uses within 500-meter radii of each well were quantified by digitizing overlays of aerial photographs that were verified and updated in the field. Concentrations of magnesium and sulfate were greater in ground water beneath areas of denser residential development, which may be a natural artifact of better drainage and a deeper water table in those areas. Frequencies of detection of some pesticides and volatile organic compounds were greater in water from wells with greater proportions of industrial and transportation land uses. Ground water in areas with less dense residential development, mostly the more recently-developed areas, tended to have greater concentrations of agricultural herbicides and some nutrients probably a relict of previous agricultural land use.

Minnesota↗

USGS1989

An investigation of shallow ground-water quality near East Fork Poplar Creek, Oak Ridge, Tennessee

Alluvial soils and fill materials in and near the floodplain of East Fork Poplar Creek in Oak Ridge, Tennessee, are contaminated with various trace metals (primarily mercury), organic compounds, and radionuclides that were lost to the stream as a result of past operations at the Y-12 Plant, a nuclear-processing facility located within the U.S. Department of Energy’s Oak Ridge Reservation. Observation wells were installed in the shallow (above bedrock) aquifer in and near the floodplain of East Fork Poplar Creek and water-quality samples were collected to determine if contaminants found in the soils and fill are also present in the shallow ground water. The shallow aquifer in the East Fork Poplar Creek flood plain consists primarily of alluvial silt and clay with lesser amounts of sand and gravel. Thickness of the shallow aquifer ranges from essentially zero to as much as 20 feet. A silty-clay glei horizon is present between the base of the alluvium and the top of bedrock at most flood-plain locations and, where present, likely impedes downward ground-water movement. Water in the shallow aquifer near East Fork Poplar Creek occurs under water-table conditions. Recharge to the shallow aquifer is principally from precipitation, and discharge is through springs and seeps to East Fork Poplar Creek and its tributaries. During spring, summer; and fall, evapotranspiration also accounts for the removal of water in storage in the shallow aquifer. Water levels in the shallow aquifer fluctuate seasonally in response to variations in recharge and evapotranspiration. Generally, the depth to water in the observation wells ranged from about 1 to 4 feet below land surface in late winter, and from about 2 to 7 feet below land surface in late fall. During extremely dry periods, the water table recedes below the top of bedrock in some flood-plain areas, possibly causing East Fork Poplar Creek to lose water to the shallow aquifer along some reaches. Contaminants found in water samples collected from several of the observation wells in concentrations (total and (or) total-recoverable) which equaled or exceeded drinking-water standards established by the U.S. Environmental Protection Agency are antimony, chromium, lead, mercury, selenium, total phenols, and strontium-90. Total and dissolved uranium concentrations exceeded 1.0 microgram per liter in samples from nearly 70 percent of the wells in the East Fork Poplar Creek flood plain. Organic compounds that were identified in low concentrations in samples from a few wells in the flood plain are: Arochlor 1260, benzo(a)anthracene, benzo(b)fluoranthene, chrysene, 3,3-dichlorobenzidine, di-n-butylphthalate, N-nitrosodiphenylamine, and pyrene. Water from one well in the East Fork Poplar Creek flood plain at a contaminated fill site contained 37and 8 micrograms per liter of trichloroethene and trans-1,2-dichloroethene, respectively. Comparison of the results of total and (or) total-recoverable trace-metal determinations with those from dissolved determinations demonstrates that elevated concentrations of these substances in water collected from several of the wells in the East Fork Poplar Creek flood plain resulted from sorption of trace metals (and possibly organic compounds and radionuclides) by fine sediment suspended in the samples. The occurrence of contaminated sediment in these samples is suspected to be the result of borehole contamination during well installation.

Tennessee↗

USGS1995

Hydrogeology and water quality at the management systems evaluation area near Piketon, Ohio

This report presents the results of a study by the U.S. Geological Survey, The Ohio State University, and the U.S. Department of Agriculture to describe the hydrology, water quality, and geochemical factors controlling water quality at the Ohio Management Systems Evaluation Area (MSEA). The Ohio MSEA is located on a 650-acre farm in the Scioto River Valley in Pike County, south-central Ohio. The farm is underlain by an incised bedrock valley filled with about 70 feet of sand and gravel outwash deposits that are covered by a veneer of silty clay alluvium and silty loam and sandy loam soils. Outwash sediment are composed predominantly of dolomite, quartz, and calcite, and have a median organic carbon concentration of 0.39 weight percent. Horizontal hydraulic conductivity of the sediment based on results of multiple-well aquifer tests ranges from 400 to 560 feet per day. Ground-water flow is from east to west-southwest at an average velocity of 1.5 to 2.5 feet per day. Ground water and surface water at the site are highly interconnected. Big Beaver Creek recharges the outwash aquifer along the eastern edge of the study area, and ground water discharges to the Scioto River at the western edge of the study area. High-stage events on the Scioto River cause frequent flow reversals in the aquifer that allow streamwater to travel a maximum observed distance of 190 feet inland. A zone of oxidizing waters (characterized by high dissolved oxygen concentration and Eh) is found in shallow ground water for several hundred feet adjacent to Big Beaver Creek and the Scioto River. This zone of oxidizing ground water is caused by the periodic inflow of surface waters to the aquifer. A ground-water budget for the study area indicates that the aquifer received 17.7 inches of recharge during water year 1992; of this amount, 72 percent originated as infiltrating precipitation, 28 percent as infiltration of surface water from Big Beaver Creek, and 0.2 percent as leakage from bedrock. Areal variation in water quality is caused by areal differences in the relative importance of these three recharge sources. The effects of bedrock leakage are evident only in the northeast corner of the study area. Here, deep outwash waters are transitional in composition between the calcium magnesium bicarbonate waters found elsewhere in the outwash aquifer and the calcium sodium chloride waters of the bedrock aquifer. Mixing calculations indicate that these deep outwash waters are composed of as much as 26 percent bedrock water. In the southern part of the MSEA, ground water is diluted by surface water from Big Beaver Creek as it recharges the aquifer through a sand and gravel streambed. At the northeast corner of the MSEA, however, Big Beaver Creek flows across a shale streambed through which no infiltration occurs. Redox reactions in the outwash aquifer control variations in aquifer chemistry with depth. From the water table to about 40 feet below land surface, oxidizing conditions are characterized by the presence of dissolved oxygen and nitrates in ground water, Eh greater than 200 millivolts, ferrihydrite coatings on sediment grains, and the absence of dissolved iron and manganese. From about 40 feet below land surface to the base of the aquifer, reducing conditions are characterized by dissolved oxygen concentrations less than 2 mg/L, Eh less than 200 millivolts, and the presence of dissolved iron and manganese. Denitrification in the reducing zone naturally remediates anthropogenic nitrate contamination of the aquifer while oxidizing pyrite in the aquifer sediment.

Ohio↗