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At least 19 recordsLinked to original sources
USGS1988

Effects of zinc smelter emissions on farms and gardens at Palmerton, PA

In 1979, before the primary Zn smelter at Palmerton was closed due to excessive Zn and Cd emissions and change in the price of Zn, we were contacted by a local veterinarian regarding death of foals (young horses) on farms near the smelter. To examine whether Zn or Cd contamination of forage or soils could be providing potentially toxic levels of Zn or other elements in the diets of foals, we measured metals in forages, soils, and feces of grazing livestock on two farms near Palmerton. The farms were about 2.5 and about 10 km northeast of the East stack. Soils, forages, and feces were greatly increased in Zn and Cd. Soil, forage, and fecal Zn were near 1000 mg/kg and Cd, 10-20 mg/kg at farm A (2.5 km) compared to normal background levels of 43 mg Zn and 0.2 mg Cd/kg, respectively. Liver and kidney of cattle raised on Farm A were increased in Zn and Cd, indicating that at least part of the Zn and Cd in smelter contaminated forages was bioavailable. During the farm sampling, we obtained soil from one garden in Palmerton within 200 m of the primary (West) smelter. The Borough surrounds the smelter facility in a valley. Because soil Cd was near 100 mg/kg, we sampled garden soils and vegetables from over 40 gardens in 6 randomly selected blocks and in rural areas at different distances from the smelter during September, 1980. All homes were contacted on each sampled block. Nearly all homes had some garden, while at least 2 appeared to grow over 50% of their annual vegetable and potato consumption. Palmerton garden soils averaged 76 mg Cd/kg and 5830 mg Zn/kg. Gardeners had been taught to add limestone and organic fertilizers to counteract yield reduction and chlorosis due to the excessive soil Zn. Gardens with over 5000 mg Zn/kg were nearly allover pH 7, and many were calcareous. Because the smelter had not yet ceased operations in 1980, crops could have been polluted by aerosol Zn and Cd emitted by the smelter. Crop Zn and Cd were extremely high, about 100 times normal Cd levels. In more distant gardens, soil metals were not so high, and gardeners had not added as much limestone. Bean rotated with the potatoes and leafy vegetables often suffered chlorosis and visible yield reduction. Potatoes contained up to 6 mg Cd/kg dry wt. compared to backgrournd 0.20 mg/kg DW. An estimate of potential Zn and Cd intakes due to the contaminated crops was made using the teen-aged male diet model, and average Cd intakes would be 250 ug/day if diets contained 100% locally grown leafy and root vegetables and potatoes. Gardeners were warned to restrict consumption of garden grown leafy and root vegetables and potatoes, and to apply 22 T/A of limestone to restrict Cd uptake. Use of improved adult diet models, and increased understanding of the effect of Zn on Cd bioavailability indicate that little Cd risk may result from consuming garden vegetables grown at Palmerton. Individuals appear to be protected because Zn accompanied crop Cd, they grew only small amounts of vegetables in most cases, and aerosol pollution of crops has ceased. Reduced Zn emissions, and Cu supplementation have prevented further health effects on foals or cattle. Detailed examination of these risks is needed to develop remedial measures for both farms and gardens in the Zn + Cd polluted soils near Zn smelters at many locations in the United States and other countries. Remedial actions are necessarary to prevent chronic Zn toxicity to crops and livestock, and minimize the risk of chronic Cd toxicity to humans who consume locally grown garden crops.

Pennsylvania↗
USGS1988

Damage to the forest ecosystem on Blue Mountain from zinc smelting

Emissions from two zinc smelters in Palmerton, Pennsylvania, have caused widespread destruction of the forest on Blue Mountain. There have been striking changes in the species composition and structure of the community of vascular plants, as well as population reductions of lichens, mosses, arthropods inhabiting the letter, and amphibians. Reductions in the populations of decomposers of organic matter have led to an accumulation of litter on the forest floor. Zinc poisoning was diagnosed in a white-tailed deer, and lead poisoning was diagnosed in a shrew. White-tailed deer also contained high concentrations of cadmium.

Trace Substances in Environmental Health↗
USGS2003

Handbook of groundwater remediation using permeable reactive barriers: Applications to radionuclides, trace metals, and nutrients

Over the last century and a half, groundwaters have become contaminated by a growing number of organic and inorganic substances ranging from petroleum-derived hydrocarbons to radioactive compounds, to cancer-causing hexavalent chromium. The importance of uncontaminated groundwater for agriculture, human consumption, and the environmental health of ecosystems is paramount to the health and productivity of industrial society. Water scientists and managers are focused on developing cost-effective methods to reverse this trend. Several methodologies have been developed, however few are as cost-effective as the use of readily available materials, such as iron and organic compost, for absorbing and isolating contaminants within the matrix of a permeable barrier. The Handbook of Groundwater Remediation using Permeable Reactive Barriers presents readers with this latest technology and developments within four main sections: 1. Innovations in Design, Construction, and Evaluation of PRBs 2. Development of Reactive Materials 3. Evaluations of Chemical and Biological Processes 4. Case Studies of Permeable Reactive Barrier Installations The Handbook is one of the first references specifically on this topic. It is an excellent fit for graduate students entering this emerging field as well as professionals conducting research or implementing this technology.

Book↗
USGS2018

Methods used for the collection and analysis of chemical and biological data for the Tapwater Exposure Study, United States, 2016–17

In 2016, the U.S. Geological Survey (USGS) Environmental Health Mission Area, initiated the Tapwater Exposure Study as part of an infrastructure project to assess human exposure to potential threats from complex mixtures of contaminants. In the pilot phase (2016), samples were collected from 11 States throughout the United States, and in the second phase (2017), the study focused on the Greater Chicago area, including North and South Chicago, Illinois, and East Chicago, Indiana. Residential tapwater samples were collected at private residences during both phases, and during the first phase, samples were collected from Federal office buildings and from one office 19-liter water-bottle source. During the second phase, raw intake and treated (pre-distributional) water samples also were collected from four drinking-water treatment facilities in the Greater Chicago area. Samples were sent to laboratories at the USGS, U.S. Environmental Protection Agency, National Institute of Environmental Health Sciences, and Colorado School of Mines Center for Environmental Risk Assessment, for potential drinking-water pathogens, chemical, and bioassay analyses. These analyses included more than 400 chemicals such as trace elements, steroid hormones, pharmaceuticals, volatile organic compounds, pesticides, per- and polyfluorinated alkyl substances, cyanotoxins, and other organic compounds. The in vitro bioassay analyses included estrogen, androgen, and glucocorticoid receptor activity.

Open-File Report↗
USGS2014

Arsenic, iron, lead, manganese, and uranium concentrations in private bedrock wells in southeastern New Hampshire, 2012-2013

Trace metals, such as arsenic, iron, lead, manganese, and uranium, in groundwater used for drinking have long been a concern because of the potential adverse effects on human health and the aesthetic or nuisance problems that some present. Moderate to high concentrations of the trace metal arsenic have been identified in drinking water from groundwater sources in southeastern New Hampshire, a rapidly growing region of the State (Montgomery and others, 2003). During the past decade (2000–10), southeastern New Hampshire, which is composed of Hillsborough, Rockingham, and Strafford Counties, has grown in population by nearly 48,700 (or 6.4 percent) to 819,100. These three counties contain 62 percent of the State’s population but encompass only about 22 percent of the land area (New Hampshire Office of Energy and Planning, 2011). According to a 2005 water-use study (Hayes and Horn, 2009), about 39 percent of the population in these three counties in southeastern New Hampshire uses private wells as sources of drinking water, and these wells are not required by the State to be routinely tested for trace metals or other contaminants. Some trace metals have associated human-health benchmarks or nonhealth guidelines that have been established by the U.S. Environmental Protection Agency (EPA) to regulate public water supplies. The EPA has established a maximum contaminant level (MCL) of 10 micrograms per liter (μg/L) for arsenic (As) and a MCL of 30 μg/L for uranium (U) because of associated health risks (U.S. Environmental Protection Agency, 2012). Iron (Fe) and manganese (Mn) are essential for human health, but Mn at high doses may have adverse cognitive effects in children (Bouchard and others, 2011; Agency for Toxic Substances and Disease Registry, 2012); therefore, the EPA has issued a lifetime health advisory (LHA) of 300 μg/L for Mn. Recommended secondary maximum contaminant levels (SMCLs) for Fe (300 μg/L) and Mn (50 μg/L) were established primarily as nonhealth guidelines—based on aesthetic considerations, such as taste or the staining of laundry and plumbing fixtures—because these contaminants, at the SMCLs, are not considered to present risks to human health. Because lead (Pb) contamination of drinking water typically results from corrosion of plumbing materials belonging to water-system customers but still poses a risk to human health, the EPA established an action level (AL) of 15 μg/L for Pb instead of an MCL or SMCL (U.S. Environmental Protection Agency, 2012). The 15-μg/L AL for Pb has been adopted by the New Hampshire Department of Environmental Services for public water systems, and if exceeded, the public water system must inform their customers and undertake additional actions to control corrosion in the pipes of the distribution system (New Hampshire Department of Environmental Services, 2013). Unlike the quality of drinking water provided by public water suppliers, the quality of drinking water obtained from private wells in New Hampshire is not regulated; consequently, private wells are sampled only when individual well owners voluntarily choose to sample them. The U.S. Geological Survey (USGS), in cooperation with the EPA New England, conducted an assessment in 2012–13 to provide private well owners and State and Federal health officials with information on the distribution of trace-metal (As, Fe, Pb, Mn, and U) concentrations in groundwater from bedrock aquifers in the three counties of southeastern New Hampshire. This fact sheet analyzes data from water samples collected by a randomly selected group of private well owners from the three-county study area and describes the major findings for trace-metal concentrations.

New Hampshire↗
USGS2009

Biogeochemical redox processes and their impact on contaminant dynamics

Life and element cycling on Earth is directly related to electron transfer (or redox) reactions. An understanding of biogeochemical redox processes is crucial for predicting and protecting environmental health and can provide new opportunities for engineered remediation strategies. Energy can be released and stored by means of redox reactions via the oxidation of labile organic carbon or inorganic compounds (electron donors) by microorganisms coupled to the reduction of electron acceptors including humic substances, iron-bearing minerals, transition metals, metalloids, and actinides. Environmental redox processes play key roles in the formation and dissolution of mineral phases. Redox cycling of naturally occurring trace elements and their host minerals often controls the release or sequestration of inorganic contaminants. Redox processes control the chemical speciation, bioavailability, toxicity, and mobility of many major and trace elements including Fe, Mn, C, P, N, S, Cr, Cu, Co, As, Sb, Se, Hg, Tc, and U. Redox-active humic substances and mineral surfaces can catalyze the redox transformation and degradation of organic contaminants. In this review article, we highlight recent advances in our understanding of biogeochemical redox processes and their impact on contaminant fate and transport, including future research needs.

Environmental Science & Technology↗
USGS2003

Pharmaceuticals, hormones, personal-care products, and other organic wastewater contaminants in water resources: Recent research activities of the U.S. Geological Survey's toxic substances hydrology program

Recent decades have brought increasing concerns for potential contamination of water resources that could inadvertently result during production, use, and disposal of the numerous chemicals offering improvements in industry, agriculture, medical treatment, and even common household products. Increasing knowledge of the environmental occurrence or toxicological behavior of these contaminants from various studies in Europe, United States, and elsewhere has resulted in increased concern for potential adverse environmental and human health effects (Daughton and Ternes, 1999). Ecologists and public health experts often have incomplete understandings of the toxicological significance of many of these contaminants, particularly long-term, low-level exposure and when they occur in mixtures with other contaminants (Daughton and Ternes, 1999; Kümmerer, 2001). In addition, these ‘emerging contaminants’ are not typically monitored or assessed in ambient water resources. The need to understand the processes controlling the transport and fate of these contaminants in the environment, and the lack of knowledge of the significance of long-term exposures have increased the need to study environmental occurrence down to trace (nanogram per liter) levels. Furthermore, the possibility that mixtures of environmental contaminants may interact synergistically or antagonistically has increased the need to characterize the types of mixtures that are found in our waters. The U.S. Geological Survey’s Toxic Substances Hydrology Program (Toxics Program) is developing information and tools on emerging water-quality issues that will be used to design and improve water-quality monitoring and assessment programs of the USGS and others, and for proactive decision-making by industry, regulators, the research community, and the public (http://toxics.usgs.gov/regional/emc.html). This research on emerging water-quality issues includes a combination of laboratory work to develop new analytical capabilities as well as field work on the occurrence, fate, and effects of these contaminants.

Geohealth News↗
USGS2009

Quality of Water from Domestic Wells in Principal Aquifers of the United States, 1991-2004

As part of the National Water-Quality Assessment Program of the U.S. Geological Survey (USGS), water samples were collected during 1991-2004 from domestic wells (private wells used for household drinking water) for analysis of drinking-water contaminants, where contaminants are considered, as defined by the Safe Drinking Water Act, to be all substances in water. Physical properties and the concentrations of major ions, trace elements, nutrients, radon, and organic compounds (pesticides and volatile organic compounds) were measured in as many as 2,167 wells; fecal indicator bacteria and radionuclides also were measured in some wells. The wells were located within major hydrogeologic settings of 30 regionally extensive aquifers used for water supply in the United States. One sample was collected from each well prior to any in-home treatment. Concentrations were compared to water-quality benchmarks for human health, either U.S. Environmental Protection Agency (USEPA) Maximum Contaminant Levels (MCLs) for public water supplies or USGS Health-Based Screening Levels (HBSLs). No individual contaminant was present in concentrations greater than available health benchmarks in more than 8 percent of the sampled wells. Collectively, however, about 23 percent of wells had at least 1 contaminant present at concentrations greater than an MCL or HBSL, based on analysis of samples from 1,389 wells in which most contaminants were measured. Radon, nitrate, several trace elements, fluoride, gross alpha- and beta-particle radioactivity, and fecal indicator bacteria were found most frequently (in one or more percent of wells) at concentrations greater than benchmarks and, thus, are of potential concern for human health. Radon concentrations were greater than the lower of two proposed MCLs (300 picocuries per liter or pCi/L) in about 65 percent of the wells and greater than the higher proposed MCL (4,000 pCi/L) in about 4 percent of wells. Nitrate, arsenic, manganese, strontium, and gross alpha-particle radioactivity (uncorrected) each were present at levels greater than MCLs or HBSLs in samples from about 5 to 7 percent of the wells; boron, fluoride, uranium, and gross beta-particle radioactivity were present at levels greater than MCLs or HBSLs in about 1 to 2 percent of the wells. Total coliform and Escherichia coli bacteria were detected in about 34 and 8 percent, respectively, of sampled wells. Thus, with the exception of nitrate and fecal indicator bacteria, the contaminants that were present in the sampled wells most frequently at concentrations greater than human-health benchmarks were naturally occurring. Anthropogenic organic compounds were frequently detected at low concentrations, using typical analytical detection limits of 0.001 to 0.1 micrograms per liter, but were seldom present at concentrations greater than MCLs or HBSLs. The most frequently detected compounds included the pesticide atrazine, its degradate deethylatrazine, and the volatile organic compounds chloroform, methyl tert-butyl ether, perchloroethene, and dichlorofluoromethane. Only 7 of 168 organic compounds were present in samples at concentrations greater than MCLs or HBSLs, each in less than 1 percent of wells. These were diazinon, dibromochloroprane, dinoseb, dieldrin, ethylene dibromide, perchloroethene, and trichloroethene. Overall, concentrations of any organic compound greater than MCLs or HBSLs were present in 0.8 percent of wells, and concentrations of any organic compound greater than one-tenth of MCLs or HBSLs were present in about 3 percent of wells. Several other properties and contaminants were measured at values or concentrations outside of recommended ranges for drinking water for aesthetic quality (for example, taste or odor) or other non-health reasons. About 16 percent of the sampled wells had pH values less than (14.4 percent) or greater than (1.9 percent) the USEPA recommended range of 6.5 to 8.5. Total dissolved solids were greater than th

Scientific Investigations Report↗
USGS2004

Water-quality characteristics and ground water quantity of the Fraser River watershed, Grand County, Colorado, 1998-2001

The U.S. Geological Survey, in cooperation with the Grand County Board of County Commissioners, conducted a 4-year study to assess ground- and surface-water-quality conditions and ground-water quantity in the 302-square-mile Fraser River watershed in north-central Colorado. The Fraser River flows north about 28 miles from the headwaters near the Continental Divide, through the towns of Winter Park, Fraser, Tabernash, and Granby, and is one of the major tributaries to the Upper Colorado River. Increasing urban development, as well as the seasonal influx of tourists, is placing more demands on the water resources in the Fraser River watershed. A ground-water sampling network of 11 wells was established to represent different aquifer systems (alluvial, Troublesome Formation, Precambrian granite), land uses (urban, nonurban), and areas with or without individual septic disposal system use. The well network was sampled for ground-water quality on a semiannual basis from August 1998 through September 2001. The sampling included field properties and the collection of water samples for analysis of major ions, trace elements, nutrients, dissolved organic carbon, bacteria, methylene blue active substances, and radon-222. One surface-water site, on the Fraser River just downstream from the town of Tabernash, Colorado, was sampled bimonthly from August 1998 through September 2001 to assess the cumulative effects of natural and human processes on water quality in the upper part of the Fraser River watershed. Surface-water-quality sampling included field properties and the collection of water-quality samples for analysis of major ions, trace elements, nutrients, organic carbon, and bacteria. Ground water was a calcium-bicarbonate type water and is suitable as a drinking-water, domestic, municipal, industrial, and irrigation source. In general, no widespread ground-water-quality problems were indicated. All pH values and concentrations of dissolved solids, chloride, fluoride, sulfate, nitrite, and nitrate in the ground-water samples met or were substantially less than U.S. Environmental Protection Agency drinking-water standards and health advisories or State of Colorado water-quality standards. Federal standards for turbidity and concentrations of iron, manganese, methylene blue active substances, and radon-222 were not met in water samples from at least one well. The only ground-water-quality concern assessed by this study is radon-222, which was detected in all radon- analyzed samples from 10 wells at levels exceeding the proposed U.S. Environmental Protection Agency drinking-water standard of 300 picocuries per liter. Concentrations of chloride, magnesium, and sulfate were statistically different (higher) in ground-water samples from wells completed in the alluvial aquifer, urbanized areas, and areas with individual septic disposal system use than those from wells completed in the Troublesome Formation, nonurban areas, and areas without individual septic disposal system use. Dissolved organic carbon concentrations were statistically higher in ground-water samples from wells completed in the alluvial aquifer and areas without individual septic disposal system use than those from wells completed in the Troublesome Formation and areas with individual septic disposal system use. Differences in dissolved organic-carbon concentrations between the latter category and areas without septic systems likely had no environmental significance. Surface water at the site Fraser River below Crooked Creek at Tabernash was a calcium-bicarbonate type water and is suitable as a drinking-water, residential, commercial, and irrigation resource. All pH values and concentrations of dissolved oxygen were within the State of Colorado instream water-quality standards, and all concentrations of chloride, sulfate, iron, manganese, un-ionized ammonia, nitrite, nitrate, and fecal coliform bacteria met State standards. Seasonal changes in the values or conc

Colorado↗
USGS1998

Environmentally critical elements in channel and cleaned samples of Illinois coals

Sixteen trace and minor elements that occur in coal are listed among 189 substances identified as ‘hazardous air pollutants’ (HAPs) in the US Clean Air Act Amendments of 1990. We investigated the occurrence and cleanability of the 16 HAPs in Illinois coals, as a contribution to the discussion about the potential effect of pending environmental regulations on the future use of these coals in power generation. The average ash content of the samples of conventionally cleaned as-shipped coals is about 20% lower than that of standard channel samples. Conventional cleaning reduces the average concentrations of As, Cd, Co, Hg, Mn, Ni, Pb, Sb and Th in the as-shipped coals by more than 20% relative to channel samples. Thus, basing assessments of health risks from emissions of HAPs during coal combustion on channel samples without appropriate adjustment would overestimate the risk. Additional cleaning by froth-flotation reduces the ash content of finely-ground as-shipped coals by as much as 76% at an 80% combustibles recovery. Although the average froth-flotation cleanability for the majority of HAPs is less than that for ash, the cleanabilities in some individual cases approaches, or even exceeds, the cleanability for ash, depending on the modes of occurrences of the elements.

Illinois↗
USGS2016

Effects of aquifer storage and recovery activities on water quality in the Little Arkansas River and Equus Beds Aquifer, south-central Kansas, 2011–14

The Equus Beds aquifer in south-central Kansas is aprimary water source for the city of Wichita. The Equus Beds aquifer storage and recovery (ASR) project was developed to help the city of Wichita meet increasing current (2016) and future water demands. The Equus Beds ASR project pumps water out of the Little Arkansas River during above-base flow conditions, treats it using drinking-water quality standards as a guideline, and recharges it into the Equus Beds aquifer for later use. Phase II of the Equus Beds ASR project currently (2016) includes a river intake facility and a surface-water treatment facility with a 30 million gallon per day capacity. Water diverted from the Little Arkansas River is delivered to an adjacent presedimentation basin for solids removal. Subsequently, waste from the surface-water treatment facility and the presedimentation basin is returned to the Little Arkansas River through a residuals return line. The U.S. Geological Survey, in cooperation with the city of Wichita, developed and implemented a hydrobiological monitoring program as part of the ASR project to characterize and quantify the effects of aquifer storage and recovery activities on the Little Arkansas River and Equus Beds aquifer water quality. Data were collected from 2 surface-water sites (one upstream and one downstream from the residuals return line), 1 residuals return line site, and 2 groundwater well sites (each having a shallow and deep part): the Little Arkansas River upstream from the ASR facility near Sedgwick, Kansas (upstream surface-water site 375350097262800), about 0.03 mile (mi) upstream from the residuals return line site; the Little Arkansas River near Sedgwick, Kans. (downstream surface-water site 07144100), about 1.68 mi downstream from the residuals return line site; discharge from the Little Arkansas River ASR facility near Sedgwick, Kansas (residuals return line site 375348097262800); 25S 01 W 07BCCC01 SMW–S11 near CW36 (MW–7 shallow groundwater well site 375327097285401); 25S01 W 07BCCC02 DMW–S10 near CW36 (MW–7 deep groundwater well site 375327097285402); 25S 01W 07BCCA01 SMW–S13 near CW36 (MW–8 shallow groundwater well site 375332097284801); and 25S 01W 07BCCA02 DMW–S14 near CW36 (MW–8 deep groundwater well site 375332097284802). The U.S. Geological Survey, in cooperation with the city of Wichita, assessed the effects of the ASR Phase II facility residuals return line discharges on stream quality of the Little Arkansas River by measuring continuous physicochemical properties and collecting discrete water-quality and sediment samples for about 2 years pre- (January 2011 through April 2013) and post-ASR (May 2013 through December 2014) Phase II facility operation upstream and downstream from the ASR Phase II facility. Additionally, habitat variables were quantified and macroinvertebrate and fish communities were sampled upstream and downstream from the ASR Phase II facility during the study period. To assess the effects of aquifer recharge on Equus Beds groundwater quality, continuous physicochemical properties were measured and discrete water-quality samples were collected before and during the onset of Phase II aquifer recharge in two (shallow and deep) groundwater wells. Little Arkansas River streamflow was about 10 times larger after the facility began operating because of greater rainfall. Residuals return line release volumes were a very minimal proportion (0.06 percent) of downstream streamflow volume during the months the ASR facility was operating. Upstream and downstream continuously measured water temperature and dissolved oxygen median differences were smaller post-ASR than pre-ASR. Turbidity generally was smaller at the downstream site throughout the study period and decreased at both sites after the ASR Phase II facility began discharging despite a median residuals return line turbidity that was about an order of magnitude larger than the median turbidity at the downstream site. Upstream and downstream continuously measured turbidity median differences were larger post-ASR than pre-ASR. Median post-ASR continuously measured nitrite plus nitrate and continuously computed total suspended solids and suspended-sediment concentrations were smaller than pre-ASR likely because of higher streamflows and dilution; whereas, median continuously computed dissolved and total organic carbon concentrations were larger likely because of higher streamflows and runoff conditions. None of the discretely measured water-quality constituents (dissolved and suspended solids, primary ions, suspended sediment, nutrients, carbon, trace elements, viral and bacterial indicators, and pesticides) in surface water were significantly different between the upstream and downstream sites after the ASR Phase II facility began discharging; however, pre-ASR calcium, sodium, hardness, manganese, and arsenate concentrations were significantly larger at the upstream site, which indicates that some water-quality conditions at the upstream and downstream sites were more similar post-ASR. Most of the primary constituents that make up dissolved solids decreased at both sites after the ASR Phase II facility began operation. Discretely collected total suspended solids concentrations were similar between the upstream and downstream sites before the facility began operating but were about 27 percent smaller at the downstream site after the facility began operating, despite the total suspended solids concentrations in the residuals return line being 15 times larger than the downstream site. Overall habitat scores were indicative of suboptimal conditions upstream and downstream from the ASR Phase II facility throughout the study period. Substrate fouling and sediment deposition mean scores indicated marginal conditions at the upstream and downstream sites during the study period, demonstrating that sediment deposition was evident pre- and post-ASR and no substantial changes in these habitat characteristics were noted after the ASR Phase II facility began discharging. Macroinvertebrate community composition (evaluated using functional feeding, behavioral, and tolerance metrics) generally was similar between sites during the study period. Fewer macroinvertebrate metrics were significant between the upstream and downstream sites post-ASR (6) than pre-ASR (14), which suggests that macroinvertebate communities were more similar after the ASR facility began discharging. Upstream-downstream comparisons in macroinvertebrate aquatic-life-support metrics had no significant differences for the post-ASR time period and neither site was fully supporting for any of the Kansas Department of Health and Environment aquatic-life-support metrics (Macroinvertebrate Biotic Index; Kansas Biotic Index with tolerances for nutrients and oxygen-demanding substances; Ephemeroptera, Plecoptera, and Trichoptera [EPT] richness; and percentage of EPT species). Overall, using macroinvertebrate aquatic life-support criteria from the Kansas Department of Health and Environment, upstream and downstream sites were classified as partially supporting before and after the onset of ASR facility operations. Fish community trophic status and tolerance groups generally were similar among sites during the study period. Fish community Little Arkansas River Basin Index of Biotic Integrity scores at the upstream and downstream sites were indicative of fair-to-good conditions before the facility began operating and decreased to fair conditions after the facility began operating. Groundwater physicochemical changes concurrent with the beginning of recharge operations at the Sedgwick basin were more pronounced in shallow groundwater. No constituent concentrations in the pre-recharge period in comparison to the post-recharge period increased to concentrations exceeding drinking water regulations; however, nitrate decreased significantly from a pre-recharge exceedance of the U.S. Environmental Protection Agency maximum contaminant level to a post recharge nonexceedance. Shallow groundwater chemical concentrations or rates of detection increased after artificial recharge began for the ions potassium, chloride, and fluoride; phosphorus and organic carbon species; trace elements barium, manganese, nickel, arsenate, arsenic, and boron; agricultural pesticides atrazine, metolachlor, metribuzin, and simazine; organic disinfection byproducts bromodichloromethane and trichloromethane; and gross beta levels. Additionally, water temperature, and pH were larger after recharge began; and total solids and slime-forming bacteria concentrations and densities were smaller. Total solids, nitrate, and selenium significantly decreased; and potassium, chloride, nickel, arsenic, fluoride, phosphorus and carbon species, and gross beta levels significantly increased in shallow groundwater after artificial recharge. Results of biological activity reaction tests indicated that water quality microbiology was different before and after artificial recharge began; at times, these differences may lead to changes in dominant bacterial populations that, in turn, may lead to formation and expansion in populations that may cause bioplugging and other unwanted effects. Calcite, iron (II) hydroxide, hydroxyapatite, and similar minerals, had shifts in saturation indices that generally were from undersaturation toward equilibrium and, in some cases, toward oversaturation. These shifts toward neutral saturation indices might suggest reduced weathering of the minerals present in the Equus Beds aquifer. Chemical weathering in the shallow parts of the aquifer may be accelerated because of the increased water temperatures and the system is more vulnerable to clogged pores and mineral dissolution as the equilibrium state is affected by recharge and withdrawal. When oversaturation is indicated for iron minerals, plugging of aquifer materials may happen.

Kansas↗
USGS1992

Ground-water-quality assessment of the central Oklahoma aquifer, Oklahoma: Hydrologic, water-quality, and quality-assurance data 1987-90

This report presents data collected from 202 wells between June 1987 and September 1990 as part of the Central Oklahoma aquifer pilot study of the National Water-Quality Assessment Program. The report describes the sampling networks, the sampling procedures, and the results of the ground-water quality and quality-assurance sample analyses. The data tables consist of information about the wells sampled and the results of the chemical analyses of ground water and quality-assurance sampling. Chemical analyses of ground-water samples in four sampling networks are presented: A geochemical network, a low-density survey bedrock network, a low-density survey alluvium and terrace deposits network, and a targeted urban network. The analyses generally included physical properties, major ions, nutrients, trace substances, radionuclides, and organic constituents. The chemical analyses of the ground-water samples are presented in five tables: (1) Physical properties and concentrations of major ions, nutrients, and trace substances; (2) concentrations of radionuclides and radioactivities; (3) carbon isotope ratios and delta values (d-values) of selected isotopes; (4) concentrations of organic constituents; and (5) organic constituents not reported in ground-water samples. The quality of the ground water sampled varied substantially. The sum of constituents (dissolved solids) concentrations ranged from 71 to 5,610 milligrams per liter, with 38 percent of the wells sampled exceeding the Secondary Maximum Contaminant Level of 500 milligrams per liter established under the Safe Drinking Water Act. Values of pH ranged from 5.7 to 9.2 units with 20 percent of the wells outside the Secondary Maximum Contaminant Level of 6.5 to 8.5 units. Nitrite plus nitrate concentrations ranged from less than 0.1 to 85 milligrams per liter with 8 percent of the wells exceeding the proposed Maximum Contaminant Level of 10 milligrams per liter. Concentrations of trace substances were highly variable, ranging from below the reporting level to concentrations over the Maximum Contaminant Levels for several constituents (arsenic, barium, cadmium, chromium, lead, and selenium). Radionuclide activities also were highly variable. Gross alpha radioactivity ranged from 0.1 to 210 picocuries per liter as 230thorium. Of the wells sampled, 20 percent exceeded the proposed Maximum Contaminant Level of 15 picocuries per liter for gross alpha radioactivity. Organic constituents were detected in 39 percent of the 170 wells sampled for organic constituents; in most cases concentrations were at or near the laboratory minimum reporting levels. Ten of the wells sampled for organic constituents had one or more constituents (chlordane, dieldrin, heptachlor epoxide, trichloroethylene, 1,1-dichloroethylene, 1,1,1-trichloroethane) at concentrations equal to or greater than the Maximum Contaminant Level or acceptable concentrations as suggested in the Environmental Protection Agency's Health Advisory Summaries. Quality-assurance sampling included duplicate samples, repeated samples, blanks, spikes, and blind samples. These samples proved to be essential in evaluating the accuracy of the data, particularly in the case of volatile organic constituents.

Oklahoma↗
USGS1971

The geochemist’s involvement with the pollution problem

The geochemist can contribute much information of value toward assessing the effect of environment, including inorganic pollution, on health. The average composition of rocks, soils, plants, and water and also the increments of inorganic substances that can be expected in geologic environments of high-metal content are essential for comparison with metal contents of these components of the environment in areas contaminated by various types of inorganic air and water pollution. Background levels of lead, zinc, nickel, chromium, copper, and manganese in soils and in four classes of vegetation have been estimated from collections that were made in remote areas presumed to be free from inorganic contamination. The trace-metal content of soils and plants varies widely in different geologic provinces of the United States; in those areas of high natural mineralization, additions of metals from man-made pollution may compound a possible hazard. Results of sampling in urban areas show that contamination of vegetation by gasoline lead can be expected for at least 1000 ft back from transportation lanes, and that the lead burden is increasing greatly with time. Ore-treatment plants can also be a source of air contamination for several miles downwind and several thousand feet in other directions. Soils of naturally high metal content in a mining district may be further contaminated with both major and minor elements from smelting operations. Recent studies show that volatile elements are released directly to the air from ore deposits in place. Concentrations of mercury, for instance, may be as much as 20 times background for several hundred feet in altitude over ore deposits in which mercury occurs as a relatively minor constituent. The source of inorganic pollution in surface drainage and also in ground water is commonly geologic, as rivers may be contaminated from coal and metal deposits in place and also from mining and smelting operations. More information of the type illustrated should be accumulated and made available to scientists who are working in environmental health, and, in particular, to those involved in the pollution problem. Only by these means can we provide a scientific basis for the enactment of realistic and effective legislation for pollution control.

Book chapter↗
USGS1995

Presence, distribution, and potential sources of nitrate and selected pesticides in the surficial aquifer along the Straight River in north-central Minnesota, 1992-93

The presence and distribution of nitrate and selected pesticides in ground water in the surficial aquifer along the Straight River in north-central Minnesota were studied. Local residents and public officials are concerned that these substances may pose a health hazard to humans and livestock. Nitrate and pesticides may move downward from cultivated croplands, livestock feedlots and manured fields, waste-water lagoons, and residential development to the ground water. Ground water near the water table ranged in nitrate-nitrogen concentration (based on median values determined for sampled monitoring wells) from less than 5 to a little greater than 20 mg/L (milligrams per liter) except for one concentration of 50 mg/L downgradient from a feedlot and manured field. Increased nitrate-nitrogen concentrations generally were coincident with cultivated croplands. Decreased nitrate-nitrogen concentrations generally were coincident with forests. Trace amounts of atrazine were detected in 4 of 8 ground-water samples collected from 8 monitoring wells screened near the water table. Detections were more frequent in cultivated croplands (detections at 3 of 5 monitoring wells) than in forests (detections at 1 of 3 monitoring wells). Atrazine concentrations ranged from 0.01 to 0.11 ( μ g/L (micrograms per liter), which are well below the MCL (Maximum Contaminant Level) of 3 μ g/L established by the USEPA (U.S. Environmental Protection Agency). Trace amounts of metolachlor and alachlor were detected in one of the samples in which atrazine was detected. MCLs for metolachlor and alachlor have not been established by the USEPA. The median nitrate-nitrogen concentration determined from sampled monitoring wells along the direction of ground-water flow through five land-use settings: (1) increased from slightly greater than 0 to 50 mg/L near the water table at a feedlot and an adjacent manured field; animal waste was a nitrate source; (2) increased from 8.0 to 16 mg/L near the water table at cultivated croplands irrigated with municipal treated waste water; fertilizer probably was a nitrate source; (3) increased from slightly greater than 0 to 14 mg/L near the bottom of the aquifer at cultivated croplands irrigated with ground water; fertilizer probably was a nitrate source; (4) increased from 1.6 to 3.7 mg/L near the water table and from slightly greater than 0 to 2.8 mg/L near the bottom of the aquifer at a residential development; septic-system leachates, and possibly lawn fertilizer, may have been nitrate sources; and (5) decreased from 14 to 2.6 mg/L near the water table at three waste-water treatment lagoons; waste water was not a nitrate source. Upgradient to downgradient mean or individual nitrogen isotope δ 15 N values in % o (delta units in parts per thousand) determined for sampled monitoring wells along the direction of ground-water flow through the five land-use settings were: (1) 5.1 % o and 4.0 % o for the feedlot and adjacent manured field; (2) 1.1 % o and 0.9 % o for the cultivated croplands irrigated with waste water; (3) 3.8 % o and 2.7 % o for the cultivated croplands irrigated with ground water; (4) 3.4 % o and 4.9 % o for the residential development; and (5) 1.7 % o and 3.0 % o for the three waste-water lagoons. Nitrate from fertilizer appeared to have been present in ground water at the waste-water lagoons, cultivated croplands irrigated with waste water, and cultivated croplands irrigated with ground water. Nitrate from soil organic matter rather than from animal waste appeared to have been present in ground water at the feedlot and adjacent manured field.

Minnesota↗
USGS2024

Assessment of per- and polyfluoroalkyl substances in water resources of New Mexico, 2020–21

Per- and polyfluoroalkyl substances (PFAS) have been detected in public and private drinking-water wells, springs, and surface waters in New Mexico; however, the presence and distribution of PFAS in water resources across the State are not well characterized. From August 2020 to October 2021, the U.S. Geological Survey, in cooperation with the New Mexico Environment Department, collected water-quality samples from groundwater and surface-water sites throughout New Mexico. One hundred and seventeen groundwater wells were sampled from unconfined water-table aquifers for PFAS and a geochemical suite including major ions, trace elements, nutrients, dissolved organic carbon (DOC), stable isotopes of oxygen and hydrogen, tritium, and carbon-14 to provide context for groundwater age and geochemical evolution. Eighteen surface-water samples were analyzed for PFAS, and select samples were analyzed for wastewater tracers, major ions, trace elements, and DOC. Blanks and replicates indicated low bias and variability for PFAS, wastewater tracers, and geochemical compounds. Twenty-seven of the 117 groundwater sites had PFAS concentrations reported above the detection level, and there were no exceedances of the 2016 U.S. Environmental Protection Agency health advisory of 70 nanograms per liter (ng/L) perfluorooctanoic acid plus perfluorooctane sulfonic acid. Twenty-two sites were resampled and showed similar signatures, excluding some springs. Total PFAS concentrations ranged from 0.91 to 80.3 ng/L. The most frequently detected PFAS at groundwater sites were perfluorobutanesulfonic acid (PFBS; 11 sites), perfluoropentanoic acid (10 sites), and perfluorohexanoic acid (9 sites). Correlations were found between certain PFAS compounds that suggest similar sources. PFAS were also correlated with tritium, DOC, and nitrate, which indicated that a presence of anthropogenic compounds could in turn indicate a likelihood of PFAS occurrence. In addition, a cluster analysis showed that varying geochemical processes and sources of anthropogenic compounds likely contribute to the PFAS signature of each groundwater sample. Surface-water samples showed variable total PFAS concentrations ranging from 1.0 to 155.4 ng/L. Sites downstream from urban areas showed numerous PFAS detections. Some undeveloped areas where minimal PFAS detections would be expected had PFAS detections. Correlations between PFAS were found that suggested similar sources. Perfluoropentanoic acid and PFBS were the most frequently detected PFAS, and PFBS had the highest single concentration of 93 ng/L. Results of the study provide an overview of PFAS occurrences in the water resources of New Mexico along with geochemical context and are used to identify areas for further scientific investigations that could further characterize PFAS occurrences in New Mexico.

New Mexico↗
USGS2022

Occurrence of per- and polyfluoroalkyl substances and inorganic analytes in groundwater and surface water used as sources for public water supply in West Virginia

Per- and polyfluoroalkyl substances (PFAS) are widely observed anthropogenic compounds found in water supplies worldwide and increasingly linked with adverse health effects in humans. In 2019, the West Virginia Legislature recognized the contamination risk to public source-water supplies posed by PFAS and passed a resolution that required a statewide PFAS study. The purpose of the resolution was to understand the occurrence and distribution of PFAS contamination throughout the State’s rivers, lakes, and groundwater aquifers. The U.S. Geological Survey has worked in cooperation with the West Virginia Department of Environmental Protection and West Virginia Department of Health and Human Resources to collect raw-water samples at 279 public-water systems across West Virginia. Public-water systems sampled for this study were identified by the West Virginia Department of Health and Human Resources and included all community water systems in the State and all daycares and schools that operate their own water systems. Raw source water was sampled for both groundwater and surface-water sites at the first available tap in the public-water system, prior to any treatment. One hundred and seventy-three samples were collected from groundwater sources and 106 samples were collected from surface-water sources. Parameters collected at the time of sampling included pH, specific conductance, water temperature, dissolved oxygen, turbidity, and alkalinity. PFAS was analyzed at all 279 sites, major ions and trace elements were analyzed at 272 sites, and nutrients were analyzed at 270 sites. The type of source water used for public supply in West Virginia is generally dependent on geology with more groundwater sites sampled in high-yield aquifers such as karst and alluvium. Surface-water sites were more evenly distributed throughout the State and are often the only source used in areas underlain by lower-yielding fractured-rock aquifers. Twenty-four percent of the sites sampled for this study had at least 1 PFAS detected, 47 of which were in groundwater sources and 20 in surface-water sources. Five sites exceeded the U.S. Environmental Protection Agency’s health advisory for combined perfluorooctanoate and perfluorooctanesulfonate concentrations of 70 nanograms per liter. These sites were located in highly susceptible karst and alluvial groundwater aquifers on the east and west sides of the State. Higher PFAS concentrations were more commonly found in groundwater than surface-water sources, and high concentrations and PFAS detections were generally concentrated in the Ohio River Valley and West Virginia’s eastern panhandle. PFAS was rarely detected in groundwater sites in fractured-rock aquifers and abandoned underground coal-mine aquifers in the Appalachian Plateaus Physiographic Province had very little PFAS detected. These data represent a baseline summary of source water in West Virginia. Additional studies may be needed to understand exposure to private homeowners with domestic-water sources, variability of PFAS concentrations over time, and PFAS in finished drinking water as evaluated by current and future drinking-water regulations.

West Virginia↗