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USGS2004

Summary of available state ambient stream-water-quality data, 1990-98, and limitations for national assessment

The investigation described in this report summarized data from State ambient stream-water-quality monitoring sites for 10 water-quality constituents or measurements (suspended solids, fecal coliform bacteria, ammonia as nitrogen, nitrite plus nitrate as nitrogen, total phosphorus, total arsenic, dissolved solids, chloride, sulfate, and pH). These 10 water-quality constituents or measurements commonly are listed nationally as major contributors to degradation of surface water. Water-quality data were limited to that electronically accessible from the U.S. Environmental Protection Agency Storage and Retrieval System (STORET), the U.S. Geological Survey National Water Information System (NWIS), or individual State databases. Forty-two States had ambient stream-water-quality data electronically accessible for some or all of the constituents or measurements summarized during this investigation. Ambient in this report refers to data collected for the purpose of evaluating stream ecosystems in relation to human health, environmental and ecological conditions, and designated uses. Generally, data were from monitoring sites assessed for State 305(b) reports. Comparisons of monitoring data among States are problematic for several reasons, including differences in the basic spatial design of monitoring networks; water-quality constituents for which samples are analyzed; water-quality criteria to which constituent concentrations are compared; quantity and comprehensiveness of water-quality data; sample collection, processing, and handling; analytical methods; temporal variability in sample collection; and quality-assurance practices. Large differences among the States in number of monitoring sites precluded a general assumption that statewide water-quality conditions were represented by data from these sites. Furthermore, data from individual monitoring sites may not represent water-quality conditions at the sites because sampling conditions and protocols are unknown. Because of these factors, a high level of uncertainty exists in a national assessment of water quality. The purpose of this report is to present a summary of electronically available State ambient stream-water-quality data for 10 selected constituents and measurements from monitoring sites with nine or more analyses for 199098 and to discuss limitations for use of the data for national assessment. These analyses were statistiscally summarized by monitoring site and State, and the results presented in tabular format. Most of the selected constituents or measurements have U.S. Environmental Protection Agency criteria or guidelines for aquatic-life or drinking-water purposes. A significant finding of this investigation is that for a large percentage of monitoring sites in the Nation, there are insufficient data to meet U.S. Environmental Protection Agency recommendations for determining if water-quality conditions are degraded and for making informed decisions regarding total maximum daily loads.

Water-Resources Investigations Report↗
USGS2002

Variability of pesticide detections and concentrations in field replicate water samples collected for the National Water-Quality Assessment Program, 1992-97

Field replicate water samples (“field replicates”) collected for the U.S. Geological Survey National Water-Quality Assessment (NAWQA) Program during 1992 to 1997 were used to assess the variability of pesticide detections and concentrations in environmental water samples collected from the surface-and ground-water-quality networks of the NAWQA Program. Field replicates are two or more identically collected, processed, and analyzed environmental water samples that are used to assess the overall variability of field and laboratory procedures. Variability is the degree of random error in independent measurements of the same quantity and is the opposite of precision—the degree of mutual agreement. Information on variability can be used to estimate the reproducibility of individual measurements, the concentration needed to be assured of exceeding a water-quality standard, and the likelihood that two measurements of water quality are different. Variability of pesticide detections was assessed by calculating the mean percentage detection of a pesticide and the percentage of inconsistent replicate sets. Variability of pesticide concentrations was assessed by pooling estimates of the standard deviation and relative standard deviation in replicate sets. Variability of pesticide detections and concentrations was a function of concentration, and estimates of variability were developed for discrete ranges of concentration. Reliability of estimates of variability was assessed by calculating 90-percent upper confidence bounds for the percentage of inconsistent replicate sets and for the pooled estimates. The variability of detection for most pesticides is high at concentrations less than the minimum reporting level, but the variability of detection decreases dramatically at higher concentrations. In view of the highly diverse sources of water submitted as field replicates for the NAWQA Program and the generally low concentrations (concentrations in 79 percent of replicate sets were less than 0.1 microgram per liter) of pesticides in most replicates, inconsistent detections in replicate sets likely were caused by variability in the analytical method and by water-matrix interferences (or other loss processes) that result in false-negative errors. Consequently, estimates of the frequency of detection of pesticides in environmental water samples collected for the NAWQA Program probably are biased low because of false-negative errors at concentrations near the minimum reporting level. Correlation analysis indicates that for most pesticides and concentrations, pooled estimates of relative standard deviation rather than pooled estimates of standard deviation should be used to estimate variability because pooled estimates of relative standard deviation are less affected by heteroscedasticity. The 2 Variability of Pesticide Detections and Concentrations in Field Replicate Water Samples, 1992–97 median pooled relative standard deviation was calculated for all pesticides to summarize the typical variability for pesticide data collected for the NAWQA Program. The median pooled relative standard deviation was 15 percent at concentrations less than 0.01 micrograms per liter (µg/L), 13 percent at concentrations near 0.01 µg/L, 12 percent at concentrations near 0.1 µg/L, 7.9 percent at concentrations near 1 µg/L, and 2.7 percent at concentrations greater than 5 µg/L. Pooled estimates of standard deviation or relative standard deviation presented in this report are larger than estimates based on averages, medians, smooths, or regression of the individual measurements of standard deviation or relative standard deviation from field replicates. Pooled estimates, however, are the preferred method for characterizing variability because they provide unbiased estimates of the variability of the population. Assessments of variability based on standard deviation (rather than variance) underestimate the true variability of the population. Because pooled estimates of variability are larger than estimates based on other approaches, users of estimates of variability must be cognizant of the approach used to obtain the estimate and must use caution in the comparison of estimates based on different approaches.

Water-Resources Investigations Report↗
USGS1977

Theoretical drawdown due to simulated pumpage from the Ohio River alluvial aquifer near Siloam, Kentucky

Theoretical drawdown due to simulated pumpage was determined for a site near Siloam, Kentucky by using a digital ground-water-flow model. The maximum sustained yield of water from the single well was shown to be less than 900 gallons per minute, and, for a simulated pumping rate of 450 gallons per minute from each of several wells, the optimum placement for either minimum water-level drawdown or minimum spacing of multiple wells was found to be in a line parallel to and at a distance of about 370 to 600 feet from the Ohio River. An analytical method was used to verify the optimum placement of wells determined by the digital model. (Woodard-USGS)

Kentucky↗
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↗
USGS1979

Chemical analyses of surface water in Illinois, 1975-77--Volume I, Des Plaines River basin and Lake Michigan

Samples of surface water were collected and analyzed by the Illinois Environmental Protection Agency. The results from water years 1975 to 1977 are presented in three volumes. The history of sampling and analytical methods used during that period 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. Volume I includes the Des Plaines River basin and Lake Michigan.

Illinois↗
USGS1979

Chemical analyses of surface water in Illinois, 1975-77--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. The results from water years 1975 to 1977 are presented in three volumes. The history of sampling and analytical methods used during that period 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. Volume II includes the Illinois River basin and Mississippi River tributaries north of Illinois River basin.

Illinois↗
USGS1979

Chemical analyses of surface water in Illinois, 1975-77--Volume III, Ohio River tributaries and Mississippi River tributaries south of Illinois River basin

Samples of surface water were collected and analyzed by the Illinois Environmental Protection Agency. The results from water years 1975 to 1977 are presented in three volumes. The history of sampling and analytical methods used during that period 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. Volume III includes Ohio River tributaries and Mississippi River tributaries south of Illinois River basin.

Illinois↗
USGS1984

Seasonal patterns of alkalinity in the San Francisco Bay estuarine system, California, during 1980

Salinity and alkalinity were measured in the near-surface waters of San Francisco Bay estuarine system at two-week intervals during 1980. Results are presented in figures and as numerical values, and the analytical methods are detailed. The transport of alkalinity to the Bay from the delta during 1980 was 3.8 x 10 to Ohe 10th power equivalents; this estimate is based on the freshwater alkalinity concentrations predicted by the north San Francisco Bay salinity-alkalinity distributions. North San Francisco Bay distributions are primarily the result of conservative mixing of freshwater from the Delta with Pacific Ocean water. Nonlinear distributions are the consequence of alkalinity variations in the freshwater rather than the effects of in-estuary processes or sources. Seasonal inflow of agricultural waste water is a major cause of freshwater alkalinity variations. South San Francisco Bay salinity-alkalinity distributions show the effects of variations in Delta outflow rate, local streams, and municipal waste-water inflows. (USGS)

Water-Resources Investigations Report↗
USGS1986

Quality of ground water in the Puget Sound region, Washington, 1981

Groundwater from more than 100 sites in the Puget Sound region, Washington, was sampled and analyzed in 1981 for pH, specific conductance, and concentrations of fecal coliform bacteria, major ions, and dissolved iron, manganese, and nitrate. 20% of the samples were analyzed for concentrations of dissolved trace metals including aluminum, arsenic, barium, cadmium, chromium, copper, lead, mercury, selenium, silver, and zinc. The predominant water types were calcium bicarbonate and calcium-magnesium bicarbonate. Some wells in San Juan and Island Counties contained sodium chloride as a result of seawater intrusion. Dissolved solids concentrations were generally < 150 mg/L. Iron concentrations > 300 micrograms/L in 14% of all samples. Manganese concentrations > 50 micrograms/L in 40% of all samples. Trace-metal concentrations were generally < 10 mg/L , except for barium, copper, lead, and zinc. Nitrate concentrations were < 1.0 mg/L in water for over 75% of the sites. Concentrations > 1.0 mg/L in samples from Skagit, Whatcom , and Pierce Counties, were probably due to agricultural activities or septic tanks. Fecal coliform bacteria were detected in isolated instances. EPA drinking water regulations were exceeded only in isolated instances, except for widespread excessive iron and manganese concentrations. The historical data for the region were also evaluated for the same constituents. There are quantitative differences between historical and 1981 data, but they may be due to inconsistencies in data collection and analytical methods.

Washington↗
USGS1986

Quality of ground water in the Columbia Basin, Washington, 1983

Groundwater from 188 sites in the Columbia Basin of central Washington was sampled and analyzed in 1983 for pH, specific conductance, and concentrations of fecal coliform bacteria, major dissolved ions, and dissolved iron, manganese, and nitrate. Twenty of the samples were also analyzed for concentrations of dissolved trace metals including aluminum, arsenic, barium, cadmium, chromium, copper, lead, mercury, selenium, silver, and zinc. The predominant water types were sodium bicarbonate and calcium bicarbonate. The sodium bicarbonate water samples had higher pH, fluoride, and sodium:adsorption ratio values than samples with other water types. Dissolved solids concentrations were generally between 250 and 500 mg/L. Iron and manganese concentrations were usually < 10 micrograms/L (ug/L). Most trace metal concentrations were also < 10 ug/L except for barium and zinc, which had maximum concentrations of 170 and 600 ug/L, respectively. Nitrate concentrations were < 1.0 mg/L in water from more than half the wells sampled. Concentrations exceeded 1.0 mg/L in large areas of Lincoln, eastern Adams, Franklin and southern Grant Counties. No fecal coliform bacteria were detected. U.S. EPA drinking water regulations were exceeded in several samples, most commonly involving pH and concentrations of fluoride, nitrate, and dissolved solids in samples from Adams and Grant Counties. Generally, the historical data lead to similar conclusions about the quality of groundwater in the Columbia Basin region. However , historical samples had higher dissolved solids concentrations in Douglas County. Historical samples also included fewer sodium bicarbonate type waters in the region as a whole than the 1983 samples. These differences may be due to inconsistencies in data collection or analytical methods. (Author 's abstract)

Water-Resources Investigations Report↗
USGS1995

Hydrogeology and simulation of flow between the alluvial and bedrock aquifers in the upper Black Squirrel Creek basin, El Paso County, Colorado

Anticipated increases in pumping from the bedrock aquifers in El Paso County potentially could affect the direction and rate of flow between the alluvial and bedrock aquifers and lower water levels in the overlying alluvial aquifer. The alluvial aquifer underlies about 90 square miles in the upper Black Squirrel Creek Basin of eastern El Paso County. The alluvial aquifer consists of unconsolidated alluvial deposits that unconformably overlie siltstones, sandstones, and conglomerate (bedrock aquifers) and claystone, shale, and coal (bedrock confining units) of the Denver Basin. The bedrock aquifers (Dawson, Denver, Arapahoe, and Laramie-Fox Hills aquifers) are separated by confining units (upper and lower Denver and the Laramie confining units) and overlie a relatively thick and impermeable Pierre confining unit. The Pierre confining unit is assumed to be a no-flow boundary at the base of the alluvial/ bedrock aquifer system. During 1949-90, substantial water-level declines, as large as 50 feet, in the alluvial aquifer resulted from withdrawals from the alluvial aquifer for irrigation and municipal supplies. Average recharge to the alluvial aquifer from infiltration of precipitation and surface water was an estimated 11.97 cubic feet per second and from the underlying bedrock aquifers was an estimated 0.87 cubic foot per second. Water-level data from eight bedrock observation wells and eight nearby alluvial wells indicate that, locally, the alluvial and bedrock aquifers probably are hydraulically connected and that the alluvial aquifer in the upper Black Squirrel Creek Basin receives recharge from the Denver and Arapahoe aquifers but-locally recharges the Laramie-Fox Hills aquifer. Subsurface-temperature profiles were evaluated as a means of estimating specific discharge across the bedrock surface (the base of the alluvial aquifer). However, assumptions of the analytical method were not met by field conditions and, thus, analyses of subsurface-temperature profiles did not reliably estimate specific discharge across the bedrock surface. The vertical hydraulic diffusivity of a siltstone and sandstone in the lower Denver confining unit was estimated, by an aquifer test, to be about 8 x 10'4 square foot per day. Physical and chemical characteristics of water from the bedrock aquifers in the study area generally differ from the physical and chemical characteristics of water from the alluvial aquifer, except for the physical and chemical characteristics of water from one bedrock well, which is completed in the Laramie-Fox Hills aquifer. In the southern part of the study area, physical and chemical characteristics of ground water indicate downward flow of water from the alluvial aquifer to the Laramie-Fox Hills aquifer. A three-dimensional numerical model was used to evaluate flow of water between the alluvial aquifer and underlying bedrock. Simulation of steady-state conditions indicates that flow from the bedrock aquifers to the alluvial aquifer was about 7 percent of recharge to the alluvial aquifer, about 0.87 cubic foot per second. The potential effects of withdrawal from the alluvial and bedrock aquifers at estimated (October 1989 to September 1990) rates and from the bedrock aquifers at two larger hypothetical rates were simulated for a 50-year projection period. The model simulations indicate that water levels in the alluvial aquifer will decline an average of 8.6 feet after 50 years of pumping at estimated October 1989 to September 1990 rates. Increases in withdrawals from the bedrock aquifers in El Paso County were simulated to: (1) Capture flow that currently discharges from the bedrock aquifers to springs and streams in upland areas and to the alluvial aquifer, (2) induce flow downward from the alluvial aquifer, and (3) accelerate the rate of waterlevel decline in the alluvial aquifer.

Colorado↗
USGS1995

Filtration of water-sediment samples for the determination of organic compounds

This report describes the equipment and procedures used for on-site filtration of surface-water and ground-water samples for determination of organic compounds. Glass-fiber filters and a positive displacement pumping system are suitable for processing most samples for organic analyses. An optional system that uses disposable in-line membrane filters is suitable for a specific gas chromatography/mass spectrometry, selected-ion monitoring analytical method for determination of organonitrogen herbicides. General procedures to minimize contamination of the samples include preparing a clean workspace at the site, selecting appropriate sample-collection materials, and cleaning of the equipment with detergent, tap water, and methanol.

Water-Resources Investigations Report↗
USGS1996

Hydrogeologic investigation and simulation of ground-water flow in the Upper Floridan Aquifer of north-central Florida and southwestern Georgia and delineation of contributing areas for selected city of Tallahassee, Florida, water-supply wells

A 4-year investigation of the Upper Floridan aquifer and ground-water flow system in Leon County, Florida, and surrounding counties of north-central Florida and southwestern Georgia began in 1990. The purpose of the investigation was to describe the ground-water flow system and to delineate the contributing areas to selected City of Tallahassee, Florida, water-supply wells. The investigation was prompted by the detection of low levels of tetrachloroethylene in ground-water samples collected from several of the city's water-supply wells. Hydrologic data and previous studies indicate that; ground-water flow within the Upper Floridan aquifer can be considered steady-state; the Upper Floridan aquifer is a single water-bearing unit; recharge is from precipitation; and that discharge occurs as spring flow, leakage to rivers, leakage to the Gulf of Mexico, and pumpage. Measured transmissivities of the aquifer ranged from 1,300 ft 2 /d (feet squared per day) to 1,300,000 ft2/d. Steady-state ground-water flow in the Upper Floridan aquifer was simulated using a three-dimensional ground- water flow model. Transmissivities ranging from less than 5,000 ft2/d to greater than 11,000,000 ft 2 /d were required to calibrate to observed conditions. Recharge rates used in the model ranged from 18.0 inches per year in areas where the aquifer was unconfined to less than 2 inches per year in broad areas where the aquifer was confined. Contributing areas to five Tallahassee water-supply wells were simulated by particle- tracking techniques. Particles were seeded in model cells containing pumping wells then tracked backwards in time toward recharge areas. The contributing area for each well was simulated twice, once assuming a porosity of 25 percent and once assuming a porosity of 5 percent. A porosity of 25 percent is considered a reasonable average value for the Upper Floridan aquifer; the 5 percent porosity simulated the movement of ground-water through only solution-enhanced bedding plains and fractures. The contributing areas were generally elliptical in shape, reflecting the influence of the sloping potentiometric surface. The contributing areas delineated for a 5 percent porosity were always much larger than those determined using a 25 percent porosity. The lowest average ground-water velocity computed within a contributing area, using a 25 percent porosity, was 1.0 ft/d (foot per day) and the highest velocity was 1.6 ft/d. The lowest average ground-water velocity, determined using a 5 percent porosity, was 2.4 ft/d and the highest was 7.4 ft/d. The contributing areas for each of the five wells was also determined analytically and compared to the model-derived areas. The upgradient width of the simulated contributing areas were larger than the upgradient width of the analytically determined contributing areas for four of the five wells. The model could more accurately delineate contributing areas because of the ability to simulate wells as partially penetrating and by incorporating complex, three-dimensional aquifer characteristics, which the analytical method could not.

Florida, Georgia↗
USGS1996

Trends in surface-water quality in Connecticut, 1969-88

Surface-water-quality data from selected monitoring stations in Connecticut were analyzed for trend, using the Seasonal Kendall test, for water years 1969-88, 1975-88, and 1981-88. The number of constituents and stations evaluated varied with the different time periods. The 39 monitoring stations included 26 freshwater streams with associated discharge data, 7 tidally affected streams, 4 harbor stations, and 2 surface impoundments. Flow-adjustment procedures were used where possible to minimize the effects of stream- flow variability on trend results. The drainage area of the monitoring stations includes approximately 5,000 mi 2 covering the State of Connecticut and about 11,000 mi 2 in upstream drainage areas outside of the State. Drainage basin size for the freshwater streams ranges from 4.1 mi 2 to 9,660 mi 2 . Land uses in the drainage basins range from undeveloped forested areas to highly urbanized metropolitan areas. During the period covered by the trend study, the State's population has grown, suburban development has increased, agricultural land use has decreased, and wastewater-treatment practices have improved. Increases in specific conductance and in the concentrations of calcium, magnesium, chloride, sulfate, dissolved solids, and total solids were geographically widespread and numerous during water years 1975-88 and indicate a general increase statewide in dissolved constituents in streamflow, both in urbanized and less developed areas. The effects of increasing urbanization, including municipal and industrial wastewater, septic system leachate, nonpoint runoff, and atmospheric deposition of contaminants, are possible causes for these increases. Decreases in turbidity and in the concentrations of total phosphorus, total organic carbon, and fecal coliform bacteria were geographically widespread and numerous during 1975-88. This general decrease in suspended material and bacteria may be attributable to basic improvements in the treatment of municipal and industrial wastewater during the period of record. Decreasing concentrations of total phosphorus may also be related to decreases in agricultural land use and to a decline in the use of detergents containing phosphorus. Detected decreases in total organic carbon and turbidity may have been caused, in part, by changes in sampling or analytical methods. Increases in total nitrogen, total organic nitrogen, and total nitrite-plus- nitrate were geographically widespread and numerous during 1975-88 and appear to indicate effects from both point sources in urbanized basins and nonpoint sources in less developed basins. The number of stations with increasing concentrations of nitrogen constituents was much smaller during 1981-88 than during 1975-88. Decreases in total ammonia nitrogen were detected at 11 stations during 1981-88. Decreases in total ammonia, sometimes paired with increases in total nitrite-plus-nitrate, may result from improvements in wastewater treatment. Increases in the concentration of dissolved oxygen, or dissolved oxygen as a percent of saturation, were geographically widespread and numerous during 1969-88 and 1975-88. Increases were less common during 1981-88. Increases in dissolved oxygen in urbanized basins may be related to major improvements in wastewater treatment during the 1970's and 1980's. The magnitude of the trends detected during 1969-88 may have been affected in part by a change, around 1974, in the model of the instrument used to measure dissolved oxygen in the field. Statewide increases in pH were detected during 1969-88, 1975-88, and 1981-88, in both urbanized and less developed basins. The widespread increases in pH were unexpected, given the relatively acidic quality of precipitation in the region during the study period. Only two decreases in pH were detected, both in relatively undeveloped basins. Increases in pH in urbanized areas may be related to decreasing concentrations of ammonia and to requirements for neutralization of municipal and industrial wastewater.

Connecticut↗
USGS1998

Surface-water quality at fixed sites in the Western Lake Michigan Drainages, Wisconsin and Michigan, and the effects of natural and human factors, 1993-95

Streamwater samples were collected from April 1993 through July 1995 at 11 fixed sites in the Western Lake Michigan Drainages Study Unit of the U.S. Geological Survey's National Water-Quality Assessment Program. Water samples were collected monthly at all Fixed Sites, and an additional two to four samples were collected each year during periods of high flow. Streamflow was monitored continuously at the Fixed Sites for the duration of the study period. This report describes field techniques used to collect the water samples, and the analytical methods used for laboratory analyses, statistical analyses of the data, and an attempt to determine the effect of natural and anthropogenic factors on concentrations of nutrients and selected major ions and suspended solids. Locations of eight of the Fixed Sites were selected to represent areas with unique combinations of land use/land cover, surficial deposits, and bedrock geology and are referred to as 'indicator sites.' The remaining three sites were located near the mouths of major rivers and are referred to as 'integrator sites.' The integrator sites represent a large part of the total flow from the Study Unit to Green Bay and western Lake Michigan, and drain various combinations of land use, bedrock, and surficial deposits. These data indicate that land use and surficial deposits may be the primary factors affecting nitrate and total phosphorus concentrations in this Study Unit. Median concentrations of nitrate at the forested sites were less than the National Median Concentration (NMC), and those at urban fixed sites were similar to the NMC. Median nitrate concentrations at the Tomorrow River, North Branch Milwaukee River, and Duck Creek agricultural indicator sites were twice the NMC, but median concentrations at the remaining agricultural indicator sites were similar to the NMC. Nitrate concentrations at one agricultural indicator site exceeded the U. S. Environmental Protection Agency (USEPA) maximum contaminant level in three run-off samples in the growing seasons of 1994 and 1995. Median concentrations of total phosphorus at the forested indicator sites were below the NMC. Tomorrow River was the only agricultural indicator site where the median total-phosphorus concentration was less than the NMC; median concentrations at the remaining agricultural Fixed Sites were similar to the NMC and exceeded 0.1 mg/L, the USEPA suggested total-phosphorus concentration in flowing water. The USEPA recommends that total-phosphorus concentration not exceed this limit to discourage excessive aquatic plant growth in flowing waters. Median total-phosphorus concentration at the urban indicator site was less than the urban NMC. Median concentrations for both nitrate and total phosphorus at the mouth of the Fox River and the Milwaukee River integrator sites were similar to the NMC for the dominant land use, agriculture, within their basins, and were lower than that at the Menominee River integrator site with a dominant forest land use. During this study, potassium concentrations were generally highest in areas of clay-dominated surficial deposits, silica was generally highest in areas of sandy surficial deposits, iron generally highest in areas of igneous/metamorphic bedrock, and calcium generally highest in areas of carbonate bedrock. The highest median fluoride concentration occurred at an urban site that receives treated water.

Michigan, Wisconsin↗
USGS1999

Use of computer programs STLK1 and STWT1 for analysis of stream-aquifer hydraulic interaction

Quantifying the hydraulic interaction of aquifers and streams is important in the analysis of stream base fow, flood-wave effects, and contaminant transport between surface- and ground-water systems. This report describes the use of two computer programs, STLK1 and STWT1, to analyze the hydraulic interaction of streams with confined, leaky, and water-table aquifers during periods of stream-stage fuctuations and uniform, areal recharge. The computer programs are based on analytical solutions to the ground-water-flow equation in stream-aquifer settings and calculate ground-water levels, seepage rates across the stream-aquifer boundary, and bank storage that result from arbitrarily varying stream stage or recharge. Analysis of idealized, hypothetical stream-aquifer systems is used to show how aquifer type, aquifer boundaries, and aquifer and streambank hydraulic properties affect aquifer response to stresses. Published data from alluvial and stratifed-drift aquifers in Kentucky, Massachusetts, and Iowa are used to demonstrate application of the programs to field settings. Analytical models of these three stream-aquifer systems are developed on the basis of available hydrogeologic information. Stream-stage fluctuations and recharge are applied to the systems as hydraulic stresses. The models are calibrated by matching ground-water levels calculated with computer program STLK1 or STWT1 to measured ground-water levels. The analytical models are used to estimate hydraulic properties of the aquifer, aquitard, and streambank; to evaluate hydrologic conditions in the aquifer; and to estimate seepage rates and bank-storage volumes resulting from flood waves and recharge. Analysis of field examples demonstrates the accuracy and limitations of the analytical solutions and programs when applied to actual ground-water systems and the potential uses of the analytical methods as alternatives to numerical modeling for quantifying stream-aquifer interactions.

Water-Resources Investigations Report↗
USGS1999

Pesticides and their metabolites in wells of Suffolk County, New York, 1998

Five insecticide residues and 20 herbicide residues were detected in water samples collected from 50 shallow wells screened in the surficial sand and gravel aquifer in Suffolk County, Long Island in areas with known or suspected residues. Laboratory analytical methods with extremely low detection limits - from 0.001 to 0.2 ?g/L (micrograms per liter) - were used to analyze the samples for 60 pesticide residues. Forty-four of the samples contained at least one pesticide residue, and some samples contained as many as 11 different pesticides or pesticide metabolites. Only four water- quality standards were exceeded in the samples collected in this study. Dieldrin exceeded the New York State Class GA standard (0.004 ?g/L) in samples from eight wells. The Federal and New York State Maximum Contaminant Level for simazine (4 ?g/L) was exceeded in samples from two wells, and the State Class GA standard for simazine (0.5 ?g/L) was exceeded in samples from six wells. Federal water-quality standards have not been established for many of the compounds detected in this study, including herbicide metabolites. Maximum concentrations of four herbicide metabolites -metolachlor ESA (ethanesulfonic acid), metolachlor OA (oxanilic acid), and the alachlor metabolites alachlor ESA and alachlor OA -exceeded 20 ?g/L. The maximum concentration of one herbicide (tebuthiuron) exceeded 10 ?g/L, and the maximum concentration of three herbicides (simazine, metolachlor, and atrazine) and one herbicide metabolite (deisopropylatrazine) ranged from 1 to 10 ?g/L. The herbicide metolachlor, which is used on potato fields in Suffolk County, and its metabolites (metolachlor ESA and metolachlor OA) were most frequently detected in samples from agricultural areas. The herbicides simazine and tebuthiuron, which were used in utility rights-of-way, and the simazine metabolite deisopropylatrazine were detected at concentrations greater than 0.05 ?g/L most frequently in samples from residential and mixed land-use areas. The results of this investigation are not necessarily representative of conditions throughout the remainder of Long Island, because these samples were collected in areas of known or suspected residues.

Water-Resources Investigations Report↗