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USGS1978

Chemical analyses of surface water in Illinois, 1958–74—Volume I, Des Plaines River basin and Lake Michigan

Samples of surface water were collected and analyzed by the Illinois Environmental Protection Agency and its predecessor, the Stream Pollution Control Bureau of the Illinois Department of Public Health. The results for the period 1958 to 1974 are presented in tabular form and the history of sampling and analytical methods are summarized. Stream discharge data from records of the U.S. Geological Survey are included for all sites where samples were collected at gaging stations or near enough that reliable discharge estimates could be made. The report is contained in three volumes. This volume (Volume I) includes Des Plaines River basin and Lake Michigan. (See also W78-10035 and W78-10036).

Illinois↗

USGS1978

Chemical analyses of surface water in Illinois, 1958–74—Volume II, Illinois River basin and Mississippi River tributaries north of Illinois River basin

Samples of surface water were collected and analyzed by the Illinois Environmental Protection Agency and its predecessor, the Stream Pollution Control Bureau of the Illinois Department of Public Health. The results for the period 1958 to 1974 are presented in tabular form and the history of sampling and analytical methods are included for all sites where samples were collected at gaging stations or near enough that reliable discharge estimates could be made. The report is contained in three volumes. This volume (Volume II) includes Illinois River basin and Mississippi River tributaries north of Illinois River basin. (See also W78-10034 and W78-10036)

Illinois↗

USGS1978

Chemical analyses of surface water in Illinois, 1958–74—Volume III, Ohio River tributaries and Mississippi River tributaries south of the Illinois River basin

Samples of surface water were collected and analyzed by the Illinois Environmental Protection Agency and its predecessor, the Stream Pollution Control Bureau of the Illinois Department of Public Health. The results for the period 1958 to 1974 are presented in tabular form and the history of sampling and analytical methods are summarized. Stream discharge data from records of the U.S. Geological Survey are included for all sites where saples were collected at gaging stations or near enough that reliable discharge estimates could be made. The report is contained in three volumes. This volume (Volume III) includes Ohio River tributaries and Mississippi River tributaries south of Illinois River basin. (See also W78-10034 and W78-10035)

Illinois↗

USGS1994

Nonpoint and Point Sources of Nitrogen in Major Watersheds of the United States

Estimates of nonpoint and point sources of nitrogen were made for 107 watersheds located in the U.S. Geological Survey's National Water-Quality Assessment Program study units throughout the conterminous United States. The proportions of nitrogen originating from fertilizer, manure, atmospheric deposition, sewage, and industrial sources were found to vary with climate, hydrologic conditions, land use, population, and physiography. Fertilizer sources of nitrogen are proportionally greater in agricultural areas of the West and the Midwest than in other parts of the Nation. Animal manure contributes large proportions of nitrogen in the South and parts of the Northeast. Atmospheric deposition of nitrogen is generally greatest in areas of greatest precipitation, such as the Northeast. Point sources (sewage and industrial) generally are predominant in watersheds near cities, where they may account for large proportions of the nitrogen in streams. The transport of nitrogen in streams increases as amounts of precipitation and runoff increase and is greatest in the Northeastern United States. Because no single nonpoint nitrogen source is dominant everywhere, approaches to control nitrogen must vary throughout the Nation. Watershed-based approaches to understanding nonpoint and point sources of contamination, as used by the National Water-Quality Assessment Program, will aid water-quality and environmental managers to devise methods to reduce nitrogen pollution.

Water-Resources Investigations Report↗

USGS1995

Water-quality characteristics of selected public recreational lakes and ponds in Connecticut

Reconnaissance limnological and lakebed-sediment surveys were conducted in Connecticut during 1989-91 by the U.S. Geological Survey, in cooperation with the Connecticut Department of Environmental Protec- tion, to evaluate water-quality characteristics of selected public recreational lakes and ponds in the State. Limnological surveys were conducted on 49 lakes and ponds selected from a list of 105 publicly owned waterbodies that qualified for water- quality assessments under Section 314 of the Federal Clean Water Act. Lakebed-sediment surveys were conducted in 9 river impoundments and 1 riverine lake below industrial areas and 2 headwater lakes in relatively pristine areas. The limnological surveys consisted of two sampling events--during spring turnover and during the summer stratifi- cation. Each sampling event included depth profiles of water temperature, specific conductance, hydrogen-ion activity, and dissolved oxygen concen- trations; measurements of Secchi disc transparency; and the collection of samples for the analyses of alkalinity, chlorophyll, phosphorus, and nitrogen concentrations. Areal extent and population density of the dominant aquatic macrophytes were qualita- tively noted during the summer sampling event. These water-quality data were used to determine the trophic classification and acidification status of the 49 lakes. The trophic classification yielded the following results: 2 oligotrophic, 8 early mesotrophic, 13 mesotrophic, 5 late mesotrophic, 10 eutrophic, and 11 highly eutrophic lakes. In terms of acidification status, 7 lakes were classified as acid threatened and 42 as not threatened. A Wilcoxon two-tailed signed rank test was used to compare data for 13 lakes and ponds from the present survey with data from the 1973-75 or 1978-79 surveys conducted by the Connecticut Agricultural Experiment Station and Connecticut Department of Environmental Protection. The test showed no significant difference at the 90 percent confidence level for spring nitrogen and summer chlorophyll-a concen- trations, a significant increase at the 90 percent confidence level in summer phosphorus concentra- tions, and a significant decrease at the 95 percent confidence level in summer transparency. For the lakebed-sediment surveys, composite-grab samples were collected from the deepest part of each lake. Samples were analyzed for arsenic, cyanide, organic and inorganic carbon, selected metals, and methylene-extractable, synthetic organic compounds classified by the U.S. Environmental Protection Agency as semi-volatile priority pollutants. Hanover Pond, Eagleville Lake, and West Thompson Lake had three of the four highest concentrations of cadmium, chromium, copper, lead, nickel, zinc, and cyanide. The four lakes with the highest concentrations of arsenic (Aspinook Pond, Fitchville Pond, Mashapaug Pond, and West Thompson Lake) are located in the eastern part of Connecticut. The three samples with the highest mercury concentrations were from Lake Lillinonah and Lake Zoar. There appears to be a positive correlation between the concentrations of cadmium, chromium, copper, lead, nickel, zinc, and cyanide. Only 15 of the 54 synthetic organic compounds analyzed for were detected in 9 of the 12 lakes sampled. Of these 15 compounds, 14 are polycyclic aromatic hydrocarbons and the 15th is a phthalate ester. Hanover Pond had the most compounds detected (9), and phenanthrene was the compound detected in the most lakes (8).

Water-Resources Investigations Report↗

USGS1983

Distribution and abundance of nesting ospreys in the United States

Nesting Ospreys (Pandion haliaetus) in the contiguous United States now number about 8,000 pairs. Five regional populations exist (in order of abundance): Atlantic Coast, Florida and Gulf Coast, Pacific Northwest, Western Interior, and Great Lakes. Pesticides severely impacted the populations in the northern portion of the Atlantic Coast (Boston to Cape May) and the Great Lakes, but both are now recovering. During recent years in the west, especially in the Western Interior, reservoirs have been responsible for a range expansion and, perhaps, a population increase. However, a strong fidelity to ancestral breeding areas (short dispersal distance) has slowed the range expansion. Unique introductions to distant reservoirs (from breeding populations) are now being made and followed with intense interest. Ospreys adapted to man, his structures, and many of his habitat changes, but proved sensitive to his chemical pollutants. These characteristics make the Osprey an excellent environmental indicator species.

Book chapter↗

USGS2025

Leisure boat harbours, hidden alien species, and pollution: A case study of Hinsholmskilen harbour (Gothenburg, Sweden)

Small leisure boat harbours have important aesthetic and recreational values in any country with a coastline. In Sweden, there are about 860 000 leisure boats, which is one of the world's highest numbers in relation to the country's population. However, small boat harbours also present a wide range of environmental problems, including the introduction of alien species and high pollution. In this study, we investigated the ecological quality status (EcoQS) of the Hinsholmskilen small boat harbour, located southwest of the city of Gothenburg (Sweden). We performed a reconnaissance survey of the harbour's previously unstudied benthic foraminiferal communities and analysed surface sediment (0–2 cm) samples for potentially toxic elements: copper (Cu), zinc (Zn), lead (Pb), cobalt (Co), nickel (Ni), chromium (Cr), mercury (Hg), and arsenic (As). The results show that, based on the total benthic foraminiferal distribution (dead and live specimens), the assemblages in Hinsholmskilen harbour represent a typical European estuarine community with highly abundant Ammonia and Elphidium species. Based on molecular and morphological data, we report the presence of two alien and putatively invasive species likely originating from Asia: Trochammina hadai and Ammonia confertitesta (phylotype T6). Both species have recently been identified elsewhere on the Swedish west coast based on molecular and morphological data but do not have a well-known distribution. The sediment analysis for potentially toxic elements showed that the harbour has good to high EcoQS corresponding to no or little deviation from reference conditions for Cd, Co, Ni, and Pb distribution. Some of the contaminants (Pb, As, Zn, and Cr) showed poor to bad EcoQS in the innermost harbour in proximity to high-pressure cleaning plants, where boats are usually lifted, cleaned, and prepared for winter storage on land. Finally, Cu and Hg showed consistently bad and poor EcoQS all over the harbour, reflecting the use of both metals as biocides in antifouling boat paints.

Gothenburg↗

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↗

USGS1987

Estimating threshold values for the land disposal of organic solvent-contaminated wastes

This paper describes conceptual and mathematical modeling approaches to evaluate environmentally suitable waste management practices that prevent ground water pollution from landfill disposal of solid wastes contaminated with organic solvents. Threshold values for disposal of solid wastes contaminated with acetone, nitrobenzene, chlorobenzene, and carbon tetrachloride were estimated using a disposal site model using a two-dimensional advection-,dispersion solute transport computer code. For example, the threshold value for disposal of carbon tetrachloride at the site model was approximately 600 g/acre, while the value for acetone was limited only by the characteristics of the waste to prevent free drainage of liquid solvent. The study indicated that the toxicity, mass loading rate, and the mass of solvent initially disposed are critical parameters determining the relative success of a given site to attenuate contaminants to environmentally acceptable levels.

Journal of Hazardous Materials↗

USGS2009

Comparing wastewater chemicals, indicator bacteria concentrations, and bacterial pathogen genes as fecal pollution indicators

The objective of this study was to compare fecal indicator bacteria (FIB) (fecal coliforms, Escherichia coli [EC], and enterococci [ENT]) concentrations with a wide array of typical organic wastewater chemicals and selected bacterial genes as indicators of fecal pollution in water samples collected at or near 18 surface water drinking water intakes. Genes tested included esp (indicating human-pathogenic ENT) and nine genes associated with various animal sources of shiga-toxin–producing EC (STEC). Fecal pollution was indicated by genes and/or chemicals for 14 of the 18 tested samples, with little relation to FIB standards. Of 13 samples with <50 EC 100 mL −1 , human pharmaceuticals or chemical indicators of wastewater treatment plant effluent occurred in six, veterinary antibiotics were detected in three, and stx 1 or stx 2 genes (indicating varying animal sources of STEC) were detected in eight. Only the EC eae A gene was positively correlated with FIB concentrations. Human-source fecal pollution was indicated by the esp gene and the human pharmaceutical carbamazepine in one of the nine samples that met all FIB recreational water quality standards. Escherichia coli rfb O157 and stx 2c genes, which are typically associated with cattle sources and are of potential human health significance, were detected in one sample in the absence of tested chemicals. Chemical and gene-based indicators of fecal contamination may be present even when FIB standards are met, and some may, unlike FIB, indicate potential sources. Application of multiple water quality indicators with variable environmental persistence and fate may yield greater confidence in fecal pollution assessment and may inform remediation decisions

Journal of Environmental Quality↗

USGS2012

Chiral pesticides: Identification, description, and environmental implications

Anthropogenic chemicals, including pesticides, are a major source of contamination and pollution in the environment. Pesticides have many positive uses: increased food production, decreased damage to crops and structures, reduced disease vector populations, and more. Nevertheless, pesticide exposure can pose risks to humans and the environment, so various mitigation strategies are exercised to make them safer, minimize their use, and reduce their unintended environment effects. One strategy that may help achieve these goals relies on the unique properties of chirality or molecular asymmetry. Some common terms related to chirality are defined in Table 1.

Archives of Environmental Contamination and Toxico↗

USGS2000

Toxicity of Anacostia River, Washington, D.C., USA, sediment fed to mute swans (Cygnus olor)

Sediment ingestion is sometimes the principal route by which waterfowl are exposed to environmental contaminants, and at severely contaminated sites waterfowl have been killed by ingesting sediment. Mute swans ( Cygnus olor ) were fed a diet for 6 weeks with a high but environmentally realistic concentration (24%) of sediment from the moderately polluted Anacostia River in the District of Columbia, USA, to estimate the sediment's toxicity. Control swans were fed the same diet without the sediment. Five organochlorine compounds were detected in the treated diets, but none of 22 organochlorine compounds included in the analyses was detected in livers of the treated swans. The concentrations of 24 polynuclear aromatic hydrocarbons measured in the treated diet were as high as 0.80 mg/kg, and they were thought to have been responsible for the observed induction of hepatic microsomal monooxygenase activity in livers. A concentration of 85 mg/kg of lead in the diet was enough to decrease red blood cell ALAD activity but was not high enough to cause more serious effects of lead poisoning. The dietary concentrations of Al, Fe, V, and Ba were high compared to the concentrations of these elements known to be toxic in laboratory feeding studies. However, the lack of accumulation in the livers of the treated swans suggested that these elements were not readily available from the ingested sediment. We did not study all potential toxic effects, but, on the basis of those that we did consider, we concluded that the treated swans were basically healthy after a chronic exposure to the sediment.

District of Columbia↗

USGS2026

Tracing mercury from land to river: Global sources, retention, and implications for sustainability

Mercury (Hg) pollution in river systems is a global sustainability challenge. Yet the transport, transformation, and retention of Hg within global rivers remain poorly quantified, particularly in regions with sparse observations such as Southeast Asia and Africa, hindering effective pollution mitigation and reinforcing geographic inequities in scientific knowledge and environmental governance. Here, we present the first global, high-resolution simulation of riverine Hg dynamics using a process-based model that traces Hg from land-based sources through river networks to the ocean. Under a realistic scenario, we estimate that ∼1900 megagrams per year (Mg/yr) of Hg enters global rivers, including 1500 Mg/yr from human-induced sources and 400 Mg/yr from soil erosion. Nearly half of this flux (∼1000 Mg/yr) is retained in reservoirs and dams, which act as major sinks. While such retention limits downstream delivery to the oceans, it also heightens in-reservoir Hg methylation risks. By bridging the gap between Hg releases and observed riverine exports, our framework offers a scalable tool for data-limited regions, promotes data access, and supports global freshwater and pollution-management strategies.

Environmental Science & Technology↗

USGS1996

Simulation of wastewater effects on dissolved oxygen during low streamflow in the Red River of the North at Fargo, North Dakota, and Moorhead, Minnesota

Pursuant to Section 303(d) of the Clean Water Act, both North Dakota and Minnesota identified part of the Red River of the North (Red River) as water-quality limited. The states are required to determine the total maximum daily load (TMDL) that can be discharged to a water-quality limited reach from various pollution sources without contravening water-quality standards (U.S. Environmental Protection Agency, 1991). A work group consisting of local, State, and Federal agency representatives that was organized in June 1994 decided that a TMDL should be developed in phases for a subreach of the Red River at Fargo, N. Dak., and Moorhead, Minn. (fig. 1). In the first phase, which is the basis for this report, the focus is on attainment of the instream dissolved-oxygen (DO) standard during low streamflows, and only Fargo and Moorhead wastewater-treatment-plant discharges and Sheyenne River inflow are considered. The study reach begins about 0.1 mile (mi) downstream (north) of the 12th Avenue North bridge in Fargo and extends 30.8 mi downstream to a site 0.8 mi upstream of the confluence of the Buffalo and Red Rivers (fig. 1). Nitrification of total ammonia (ammonia) from Fargo and Moorhead wastewater consumes most of the DO in the study reach (Wesolowski, 1994). Because the new (1995) Fargo plant already is nitrifying its wastewater, the work group needed to determine the maximum ammonia concentration for wastewater from the nonnitrifying Moorhead plant. To accomplish this task, the Red River at Fargo Water-Quality (RRatFGO QW) model (Wesolowski, 1994, 1996b) was used to simulate the effects of various wastewater-management alternatives during low streamflow. This report presents the results of those simulations to determine the usefulness of the model for management decisions. The simulations and report were completed in cooperation with the North Dakota Department of Health.

Minnesota↗

USGS2000

A Synopsis of Technical Issues for Monitoring Sediment in Highway and Urban Runoff

Accurate and representative sediment data are critical for assessing the potential effects of highway and urban runoff on receiving waters. The U.S. Environmental Protection Agency identified sediment as the most widespread pollutant in the Nation's rivers and streams, affecting aquatic habitat, drinking water treatment processes, and recreational uses of rivers, lakes, and estuaries. Representative sediment data are also necessary for quantifying and interpreting concentrations, loads, and effects of trace elements and organic constituents associated with highway and urban runoff. Many technical issues associated with the collecting, processing, and analyzing of samples must be addressed to produce valid (useful for intended purposes), current, complete, and technically defensible data for local, regional, and national information needs. All aspects of sediment data-collection programs need to be evaluated, and adequate quality-control data must be collected and documented so that the comparability and representativeness of data obtained for highway- and urban-runoff studies may be assessed. Collection of representative samples for the measurement of sediment in highway and urban runoff involves a number of interrelated issues. Temporal and spatial variability in runoff result from a combination of factors, including volume and intensity of precipitation, rate of snowmelt, and features of the drainage basin such as area, slope, infiltration capacity, channel roughness, and storage characteristics. In small drainage basins such as those found in many highway and urban settings, automatic samplers are often the most suitable method for collecting samples of runoff for a variety of reasons. Indirect sediment-measurement methods are also useful as supplementary and(or) surrogate means for monitoring sediment in runoff. All of these methods have limitations in addition to benefits, which must be identified and quantified to produce representative data. Methods for processing raw sediment samples (including homogenization and subsampling) for subsequent analysis for total suspended solids or suspended-sediment concentration often increase variance and may introduce bias. Processing artifacts can be substantial if the methods used are not appropriate for the concentrations and particle-size distributions present in the samples collected. Analytical methods for determining sediment concentrations include the suspended-sediment concentration and the total suspended solids methods. Although the terms suspended-sediment concentration and total suspended solids are often used interchangeably to describe the total concentration of suspended solid-phase material, the analytical methods differ and can produce substantially different results. The total suspended solids method, which commonly is used to produce highway- and urban-runoff sediment data, may not be valid for studies of runoff water quality. Studies of fluvial and highway-runoff sediment data indicate that analyses of samples by the total suspended solids method tends to under represent the true sediment concentration, and that relations between total suspended solids and suspended-sediment concentration are not transferable from site to site even when grain-size distribution information is available. Total suspended solids data used to calculate suspended-sediment loads in highways and urban runoff may be fundamentally unreliable. Consequently, use of total suspended solids data may have adverse consequences for the assessment, design, and maintenance of sediment-removal best management practices. Therefore, it may be necessary to analyze water samples using the suspended-sediment concentration method. Data quality, comparability, and utility are important considerations in collection, processing, and analysis of sediment samples and interpretation of sediment data for highway- and urban-runoff studies. Results from sediment studies must be comparable and readily transf

Open-File Report↗

USGS2002

Water-quality parameters and benthic algal communities at selected streams in Minnesota, August 2000 - Study design, methods and data

Water-quality measurements and benthic algal samples were measured or collected from select Minnesota streams as part of a multiagency (Minnesota Pollution Control Agency, Minnesota Department of Natural Resources, U.S. Environmental Protection Agency, and U.S. Geological Survey) study. The goal of the multiagency study was to identify quantifiable thresholds of water-quality impairment and establish quantifiable indicators of nutrient enrichment for medium to high-order streams. This report describes the study design, sampling methods, and summarizes the physical, chemical, and benthic algal data for a component of the multiagency study that was designed to document diurnal water-quality measurements (specific conductance, pH, water temperature, and dissolved oxygen), benthic algal community composition and chlorophyll-a content, and primary productivity at 12 stream sites on 6 streams in Minnesota during August 2000. Specific conductance, pH, water temperature, dissolved oxygen concentrations and percent dissolved oxygen saturation measurements were made with submersible data recorders at 30 minute intervals for a period of 3-6 days during August 2000. Benthic algae collected from wood and rock substrate were identified and enumerated. Biovolume (volume of algal cells per unit area), density (number of cells per unit area), and chlorophyll-a content from benthic algae were determined. These data can be used as part of the multiagency study to develop an understanding of the relations among nutrient concentrations, algal abundance, algal community composition, and primary production and respiration processes in rivers of differing ecoregions in Minnesota.

Minnesota↗

USGS2015

Water use in Georgia by county for 2010 and water-use trends, 1985–2010

Water use and water withdrawals and returns in 2010 are estimated for each major river basin, principal aquifer, water-planning region, and county in Georgia using data obtained from various Federal and State agencies and local sources. Offstream water use in 2010 is estimated for the categories of public supply, domestic, commercial, industrial, mining, irrigation, livestock, aquaculture, and thermoelectric power. Water-use trends for 1985 to 2010 are also shown. The period between 2007 and 2010 was a challenging time economically and climatologically in Georgia. During that period, the United States was in the midst of a major recession, resulting in decreases in the manufacturing and construction industries and large increases in unemployment. During 2007, 2008, and the latter half of 2010, precipitation in Georgia was substantially below the 30-year norm. According to the 2010 Census of Population and Housing, nearly 9.7 million people lived in Georgia. The water for about 85 percent of that population was provided by public water suppliers. Estimated total water withdrawals from ground-water and surface-water sources were about 4,670 million gallons per day (Mgal/d) in 2010, about a 15-percent reduction from 2005 (5,471 Mgal/d). In 2010, thermoelectric-power facilities (2,046 Mgal/d) and public-supply uses (1,121 Mgal/d) accounted for 68 percent of all water withdrawn in Georgia. Surface-water withdrawals were greatest for thermoelectric-power generation (2,043 Mgal/d), whereas irrigation used the largest amount of groundwater (599 Mgal/d). Surface water provided 78 percent of the 1,121 Mgal/day withdrawn for public supply in 2010. Typically, counties in northern Georgia withdraw a larger percentage of water from surface water than groundwater sources; whereas, counties in the southern part of the State withdraw more water from groundwater sources. Historically, water withdrawals in Georgia were highest in 1980 (6,725 Mgal/d). By 1990, water use had decreased by 20 percent to 5,353 Mgal/d, but increased to 6,487 Mgal/d in 2000. By 2005, water use had decreased to an estimated 5,471 Mgal/d, and declined further to 4,670 Mgal/d in 2010—a 30-percent decrease since 1980. This decline was evident across all water-use categories, but was greatest for surface-water withdrawals by thermoelectric-power facilities. The estimated total water use per capita in 1985 (total withdrawals for all categories divided by total population) was about 850 gallons per day (gal/d), steadily decreasing to about 798 gal/d in 2000, and decreasing further to 460 gal/d in 2010. Although water use declined among all use categories during that 10-year period, most of the decline in per capita water use was caused by the large decrease in water used for thermoelectric-power generation. Throughout 1985–2010 water withdrawn for thermoelectric-power generation has constituted the largest volume of offstream water use in Georgia. Total withdrawals for thermoelectric-power generation declined about 37 percent between 2000 and 2010, mostly due to the decommissioning of power plants in the State. Also during this period, several power plants were shut down and re-tooled to use natural gas-powered generators; thus, water withdrawals for cooling were substantially reduced. The decline in water withdrawals and use between 2005 and 2010 can probably be attributed to several factors working together during this period: (1) water conservation laws and policies along with advances in water-conservation technology; (2) the onset of a major recession in 2007; and (3) below average rainfall in 2007, 2008, and the latter half of 2010. Because of these factors, water withdrawn by public suppliers decreased by 4.8 percent (despite a nearly 11-percent increase in population served) and per capita use decreased by 19 percent between 2005 and 2010. About 2,225 Mgal/d of water was returned to Georgia streams and lakes in 2010 under the National Pollutant Discharge Elimination System program administered by the Georgia Environmental Protection Division. This amount is about 48 percent of the total water withdrawn from all sources in 2010. Water returns declined 39 percent between 1995 and 2010, mirroring the decline in water withdrawals during that period. In addition, land applications of treated wastewater increased steadily between 1995 and 2010.

Georgia↗

USGS1999

Selected elements and organic chemicals in bed sediment and fish tissue of the Tualatin River basin, Oregon, 1992-96

A variety of elements and organic compounds have entered the environment as a result of human activities. Such substances find their way to aquatic sediments from direct discharges to waterways, atmospheric emissions, and runoff. Some of these chemicals are known to harm fish or wildlife, either by direct toxicity, by reducing viability, or by limiting reproductive success. In aquatic systems, sediments become the eventual sink for most of these chemicals. Analyzing the sediments provides a first step in a chemical inventory that can lead to an assessment of potential biological impacts (Kennicutt and others, 1994). Many elements (iron, aluminum, calcium, and others) enter the environment from the natural weathering of rock. Additional amounts of elements have been contributed by human activities such as mining, metals production and processing, fossil fuel combustion, municipal waste incineration, and transportationrelated sources. The environmental presence of some elements, such as lead and mercury, is almost entirely due to human activity. Lead is often associated with the use of leaded gasoline and from the manufacture and disposal of lead storage batteries. Mercury was used historically in a variety of industrial processes and as a pesticide. Nriagu and Pacyna (1998) concluded that human activity is the “most important element in the global biogeochemical cycling of the trace metals.” The number of organic compounds in existence and their total production has more than tripled in the last century. Many of these compounds enter the environment directly as pesticides; others are inadvertently discharged. Some organic compounds have natural sources. Three general classes of organic compounds will be discussed: organochlorine compounds, polyaromatic hydrocarbons, and phthalates. Almost all organochlorine compounds are manmade. Many are pesticides that were used widely in the 1950s–60s (DDT and chlordanes, for example). Use of most organochlorine pesticides was restricted or banned in the United States in the 1970s–80s. Polychlorinated biphenyls (PCBs) are also organochlorine compounds; they were used for a variety of applications, but most commonly as insulators in electrical transformers and other equipment. In general, organochlorine compounds degrade very slowly in the environment and therefore, are routinely found in environmental samples, despite the fact that they are no longer used in the United States. They are hydrophobic that is they do not dissolve readily in water and, in aquatic systems, are almost exclusively associated with sediments or tissue. Because these compounds cause a variety of adverse health effects in wildlife, the U.S. Environmental Protection Agency (USEPA) has listed many as priority pollutants. Organochlorine compounds also have been implicated as endocrine disrupters— chemicals that can interfere with the normal function of hormones. Polyaromatic hydrocarbons (PAHs) are found in sediments throughout the world (Hites and others, 1980). Their presence is thought to be primarily anthropogenic. PAHs occur naturally in petroleum products and also are produced during combustion. They enter the environment from fuel spills, tar coatings, coal and other fossil fuel usage, road dust, and from the atmospheric deposition of combustion products (Prahl and others, 1984; Wakeham and others, 1980). Urban areas often have high concentrations of PAHs because of transportation-related sources (vehicle exhaust, paving materials, and releases of fuel or oil). Natural sources, such as forest fires, may contribute small amounts of PAHs. Several PAHs are known carcinogens (benzo[a]pyrene, for example); 16 are listed as USEPA priority pollutants. Phthalate compounds are often associated with urban areas. They are used in a wide variety of industrial applications and in inks, adhesives, resins, and as plasticizers (chemicals that increase the flexibility of plastics). In aquatic systems, phthalates are found mostly in sediments where they degrade very slowly. Phthalates are thought to be endocrine disrupters; Jobling and others (1995) found that some phthalates were weakly estrogenic. USEPA considers some phthalates to be possible carcinogens. This report describes the results of a reconnaissance survey of elements and organic compounds found in bed sediment and fish tissue in streams of the Tualatin River Basin. The basin is in northwestern Oregon to the west of the Portland metropolitan area (fig. 1). The Tualatin River flows for about 80 miles, draining an area of about 712 square miles, before it enters the Willamette River. Land use in the basin changes from mostly forested in the headwaters, to mixed forest and agriculture, to predominately urban. The basin supports a growing population of more than 350,000 people, most of whom live in lower parts of the basin. Water quality in the Tualatin River and its tributaries is expected to be affected by the increasing urbanization of the basin.

Oregon↗