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At least 1,459 records · Page 81Linked to original sources
USGS1996

Field screening of water quality, bottom sediment, and biota associated with irrigation drainage in and near Walker River Indian Reservation, Nevada 1994-95

A study was begun in 1994 to determine whether the quality of irrigation drainage from the Walker River Indian Reservation, Nevada, has caused or has potential to cause harmful effects on human health or on fish and wildlife, or may adversely affect the suitability of the Walker River for other beneficial uses. Samples of water, bottom sediment, and biota were collected during June-August 1994 (during a drought year) from sites upstream from and on the Walker River Indian Reservation for analyses of trace elements. Other analyses included physical characteristics, major dissolved constituents, selected species of water-soluble nitrogen and phosphorus, and selected pesticides in bottom sediment. Water samples were collected again from four sites on the Reservation in August 1995 (during a wetterthan- average year) to provide data for comparing extreme climatic conditions. Water samples collected from the Walker River Indian Reservation in 1994 equaled or exceeded the Nevada water-quality standard or level of concern for at least one of the following: water temperature, pH, dissolved solids, unionized ammonia, phosphate, arsenic, boron, chromium, lead, and molybdenum; in 1995, only a single sample from one site exceeded a Nevada water-quality standard for molybdenum. Levels of concern for trace elements in bottom sediment collected in 1994 were equaled or exceeded for arsenic, iron, manganese, and zinc. Concentrations of organochiorine pesticide residues in bottom sediment were below analytical reporting limits. Levels of concern for trace-elements in samples of biota were equaled or exceeded for arsenic, boron, copper, and mercury. Results of toxicity testing indicate that only water samples from Walker Lake caused a toxic response in test bacteria. Arsenic and boron concentrations in water, bottom sediment, and biological tissue exceeded levels of concern throughout the Walker River Basin, but most commonly in the lower Walker River Basin. Mercury also was elevated in several biological samples collected throughout the Basin, although concentrations in water and bottom sediment were below analytical reporting limits. Sources of arsenic, boron, and mercury in the Basin are uncertain, but ambient levels reported for a variety of sample matrices collected from western Nevada generally exceed ranges cited as natural background levels. Because these potentially toxic constituents exceeded concern levels in areas that do not directly receive irrigation drainage, concentrations measured in samples collected for this study may not necessarily be attributable to agricultural activities. Diversion of river water for irrigation may have greater effects on beneficial uses of water and on fish and wildlife than does drainage from agricultural areas on the Reservation. In 1994, agricultural water consumption precluded dilution of ground-water seepage to the river channel. This resulted in concentrations of potentially toxic solutes that exceeded levels of concern. Diversion of irrigation water also may have facilitated leaching of potentially toxic solutes from irrigated soil on the Reservation, but during this study all water applied for irrigation on the Reservation was either consumed by evapotranspiration or infiltrated to recharge shallow ground water. No irrigation drainage was found on the Reservation during this study. However, because 1994 samples of ground-water seepage to the Walker River channel exceeded at least six Nevada waterquality standards, water-quality problems may result should ground-water levels rise enough to cause ground-water discharge to the agricultural drain on the Reservation. Nevertheless, the potential for adverse effects from irrigation drainage on the Reservation is believed to be small because surface-water rights for the Walker River Indian Reservation amount to only 2 percent of total surface- water rights in the entire Walker River Basin.

California, Nevada↗
USGS2001

Estimated loads and yields of suspended solids and water-quality constituents in Kentucky streams

Loads and yields of suspended solids, nutrients, major ions, trace elements, organic carbon, fecal coliform, dissolved oxygen, and alkalinity were estimated for 22 streams in 11 major river basins in Kentucky. Mean daily discharge was estimated at ungaged stations or stations with incomplete discharge records using drainage-area ratio, regression analysis, or a combination of the two techniques. Streamflow was partitioned into total and base flow and used to estimate loads and yields for suspended solids and water-quality constituents by use of the ESTIMATOR and FLUX computer programs. The relative magnitude of constituent transport to streams from groundand surface-water sources was determined for the 22 stations. Nutrient and suspended solids yields for drainage basins with relatively homogenous land use were used to estimate the total-flow and base-flow yields of nutrient and suspended solids for forested, agricultural, and urban land. Yields of nutrients?nitrite plus nitrate, ammonia plus organic nitrogen, and total phosphorus?in forested drainage basins were generally less than 1 ton per square mile per year ((ton/mi2)/yr) and were generally less than 2 (ton/mi2)/yr in agricultural drainage basins. The smallest total-flow yields for nitrogen (nitrite plus nitrate) was estimated at Levisa Fork at Paintsville in which 95 percent of the land is forested. This site also had one of the smallest total-flow yields for ammonia plus organic nitrogen. In general, nutrient yields from forested lands were lower than those from urban and agricultural land. Some of the largest estimated total-flow yields of nutrients among agricultural basins were for streams in the Licking River Basin, the North Fork Licking River near Milford, and the South Fork Licking River at Cynthiana. Agricultural land constitutes greater than 75 percent of the drainage area in these two basins. Possible sources of nutrients discharging into the Licking River are farm and residential fertilizers. Estimated base-flow yields of suspended solids and nutrients at several basins in the larger Green River and Lower Cumberland River Basins were about half of their estimated total-flow yields. The karst terrain in these basins makes the ground water highly susceptible to contamination, especially if a confining unit is thin or absent.

Kentucky↗
USGS2011

Water quality of the Chokosna, Gilahina, Lakina Rivers, and Long Lake watershed along McCarthy Road, Wrangell-St. Elias National Park and Preserve, Alaska, 2007-08

The Chokosna, Gilahina, and Lakina River basins, and the Long Lake watershed are located along McCarthy Road in Wrangell–St. Elias National Park and Preserve. The rivers and lake support a large run of sockeye (red) salmon that is important to the commercial and recreational fisheries in the larger Copper River. To gain a better understanding of the water quality conditions of these watersheds, these basins were studied as part of a cooperative study with the National Park Service during the open water periods in 2007 and 2008. Water type of the rivers and Long Lake is calcium bicarbonate with the exception of that in the Chokosna River, which is calcium bicarbonate sulfate water. Alkalinity concentrations ranged from 63 to 222 milligrams per liter, indicating a high buffering capacity in these waters. Analyses of streambed sediments indicated that concentrations of the trace elements arsenic, chromium, and nickel exceed levels that might be toxic to fish and other aquatic organisms. However, these concentrations reflect local geology rather than anthropogenic sources in this nearly pristine area. Benthic macroinvertebrate qualitative multi-habitat and richest targeted habitat samples collected from six stream sites along McCarthy Road indicated a total of 125 taxa. Insects made up the largest percentage of macroinvertebrates, totaling 83 percent of the families found. Dipterans (flies and midges) accounted for 43 percent of all macroinvertebrates found. Analysis of the macroinvertebrate data by non-metric multidimensional scaling indicated differences between (1) sites at Long Lake and other stream sites along McCarthy Road, likely due to different basin characteristics, (2) the 2007 and 2008 data, probably from the higher rainfall in 2008, and (3) macroinvertebrate data collected in south-central Alaska, which represents a different climate zone. The richness, abundance, and community composition of periphytic algae taxa was variable between sampling sites. Taxa richness and diversity were highest at the Long Lake outflow site, suggesting that the lake may have contributed planktonic taxa to the periphytic community and (or) created physical and chemical conditions at the outlet that were favorable to a variety of taxa. Long Lake is fed by groundwater and by clear water (non glacial) streams, resulting in relatively high Secchi-disc readings ranging from 17.5 to 23 feet. Depth profiles of water temperature in the lake show a strong stratification during the summer from the surface to about 13 feet, with temperatures ranging from 16 to 5 °C. Depth profiles of dissolved oxygen in the lake show a strong stratification between 26 and 33 feet, below which the concentrations of dissolved oxygen decrease from 10 to 2 milligrams per liter. Because the Long Lake outlet stream supports a large run of sockeye salmon and water temperature is an important factor during its life cycle, a logistic model was used to simulate 1998–2006 water temperatures at this site. Analysis of simulation results for 1998–2008 indicated no significant trends in water temperature. 2007 water temperatures were the highest during the 10-year period.

Alaska↗
USGS1997

Water-quality trends for streams and reservoirs in the Research Triangle area of North Carolina, 1983-95

Water-quality and streamflow monitoring data, collected from 1983 to 1995, were analyzed for 34 stream and reservoir sites in a seven-county region within the upper Neuse and upper Cape Fear River Basins. Early data (1983-88) were compiled from U.S. Geological Survey water-quality studies and from the ambient water-quality monitoring network of the North Carolina Department of Environment, Health, and Natural Resources. Analyses of major ions, nutrients, metals, trace elements, and synthetic organic compounds were compiled from samples collected by the U.S. Geological Survey from 1988 to 1995 as part of a continuing project to monitor the water quality of surface-water supplies in the Research Triangle area of North Carolina, and from the North Carolina Department of Environment, Health, and Natural Resources ambient water-quality monitoring network. This report presents the results of analysis of consistently increasing or decreasing trends in concentrations of nitrogen and phosphorus species, suspended sediment, suspended solids, sodium, chloride, iron, manganese, zinc, and chlorophyll a from seasonal Kendall trend analysis on flow-adjusted concentrations for streams and concentrations in lakes. Total phosphorus concentrations also were tested for a step decrease in concentration (step trend) associated with the North Carolina phosphate-detergent ban of 1988. For some other constituents, insufficient data or values below laboratory detection limits precluded trend analysis. A regionwide decrease in total phosphorus, ranging from 25 to 81 percent, was observed that coincided with increased phosphorus removal efforts at municipal wastewater-treatment facilities in the region and the statewide phosphate-detergent ban. Most sites had stable or decreasing trends in nitrogen concentrations; however, increasing trends occurred in the Neuse River near Clayton and at Smithfield, both of which are downstream from the developing Raleigh-Durham area. Chlorophyll a concentrations have increased by 17 to 52 percent per year at monitored reservoirs, except at Cane Creek Reservoir and Lake Michie where there was no trend. No significant trends in suspended-sediment concentrations were observed. Long-term sodium concentrations were available for only a few sites. Of these, decreasing concentrations were observed in the Neuse River at Smithfield and Cane Creek near Orange Grove, and an increasing concentration was observed in University Lake. At most sites, concentrations of manganese, iron, and zinc were stable. Decreasing iron trends were observed in Little River and Cane Creek Reservoirs and Lake Michie. Cane Creek Reservoir also had a decreasing manganese trend. Seven sites, all downstream from wastewater-treatment facilities, were analyzed for zinc trends. A decreasing trend was observed in two of these--Knap of Reeds Creek and Little Lick Creek.

North Carolina↗
USGS2023

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

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

Montana↗
USGS2013

Groundwater quality and the relation between pH values and occurrence of trace elements and radionuclides in water samples collected from private wells in part of the Kickapoo Tribe of Oklahoma Jurisdictional Area, central Oklahoma, 2011

From 1999 to 2007, the Indian Health Service reported that gross alpha-particle activities and concentrations of uranium exceeded the Maximum Contaminant Levels for public drinking-water supplies in water samples from six private wells and two test wells in a rural residential neighborhood in the Kickapoo Tribe of Oklahoma Jurisdictional Area, in central Oklahoma. Residents in this rural area use groundwater from Quaternary-aged terrace deposits and the Permian-aged Garber-Wellington aquifer for domestic purposes. Uranium and other trace elements, specifically arsenic, chromium, and selenium, occur naturally in rocks composing the Garber-Wellington aquifer and in low concentrations in groundwater throughout its extent. Previous studies have shown that pH values above 8.0 from cation-exchange processes in the aquifer cause selected metals such as arsenic, chromium, selenium, and uranium to desorb (if present) from mineral surfaces and become mobile in water. On the basis of this information, the U.S. Geological Survey, in cooperation with the Kickapoo Tribe of Oklahoma, conducted a study in 2011 to describe the occurrence of selected trace elements and radionuclides in groundwater and to determine if pH could be used as a surrogate for laboratory analysis to quickly and inexpensively identify wells that might contain high concentrations of uranium and other trace elements. The pH and specific conductance of groundwater from 59 private wells were measured in the field in an area of about 18 square miles in Lincoln and Pottawatomie Counties. Twenty of the 59 wells also were sampled for dissolved concentrations of major ions, trace elements, gross alpha-particle and gross beta-particle activities, uranium, radium-226, radium-228, and radon-222 gas. Arsenic concentrations exceeded the Maximum Contaminant Level of 10 micrograms per liter in one sample having a concentration of 24.7 micrograms per liter. Selenium concentrations exceeded the Maximum Contaminant Level of 50 micrograms per liter in one sample having a concentration of 147 micrograms per liter. Both samples had alkaline pH values, 8.0 and 8.4, respectively. Uranium concentrations ranged from 0.02 to 383 micrograms per liter with 5 of 20 samples exceeding the Maximum Contaminant Level of 30 micrograms per liter; the five wells with uranium concentrations exceeding 30 micrograms per liter had pH values ranging from 8.0 to 8.5. Concentrations of uranium and radon-222 and gross alpha-particle activity showed a positive relation to pH, with the highest concentrations and activity in samples having pH values of 8.0 or above. The groundwater samples contained dissolved oxygen and high concentrations of bicarbonate; these characteristics are also factors in increasing uranium solubility. Concentrations of radium-226 and radium-228 (combined) ranged from 0.03 to 1.7 picocuries per liter, with a median concentration of 0.45 picocuries per liter for all samples. Radon-222 concentrations ranged from 95 to 3,600 picocuries per liter with a median concentration of 261 picocuries per liter. Eight samples having pH values ranging from 8.0 to 8.7 exceeded the proposed Maximum Contaminant Level of 300 picocuries per liter for radon-222. Eight samples exceeded the 15 picocuries per liter Maximum Contaminant Level for gross alpha-particle activity at 72 hours (after sample collection) and at 30 days (after the initial count); those samples had pH values ranging from 8.0 to 8.5. Gross beta-particle activity increased in 15 of 21 samples during the interval from 72 hours to 30 days. The increase in gross beta-particle activity over time probably was caused by the ingrowth and decay of uranium daughter products that emit beta particles. Water-quality data collected for this study indicate that pH values above 8.0 are associated with potentially high concentrations of uranium and radon-222 and high gross alpha-particle activity in the study area. High pH values also are associated with potentially high concentrations of arsenic, chromium, and selenium in groundwater when these elements occur in the aquifer matrix along groundwater-flow paths.

Oklahoma↗
USGS1988

Surface-water quality of the Cedar River basin, Iowa-Minnesota, with emphasis on the occurrence and transport of herbicides, May 1984 through November 1985

The surface-water quality in the Cedar River basin was evaluated by analyzing the occurrence, distribution, and transport of common inorganic constituents and selected trace inorganic and organic constituents, with emphasis on herbicides. The surface-water quality of the Cedar River basin was monitored from May 1984 through November 1985. Depth integrated surface-water samples generally were collected monthly at six stations for a considerable range of river discharge. Samples were analyzed for concentrations of common inorganic constituents in the dissolved phase and for concentrations of primary nutrients, trace elements, organic carbon, and herbicides in the dissolved and the dissolved plus suspended phases. Water in the Cedar River was determined to be a calcium bicarbonate type; suspended-sediment concentrations ranged from 3 to 676 milligrams per liter. Concentrations of dissolved fluoride, dissolved nitrite plus nitrate, dissolved arsenic, dissolved lead, and dissolved mercury were less than those of the U.S. Environmental Protection Agency's drinking-water standards for public water supplies. Generally, herbicides were detected only in the dissolved phase, which indicates that herbicides are not being adsorbed on the suspended sediment. However, the lack of detection of adsorbed herbicides also may indicate a need for re-examination of traditionally acceptable methods of treating water samples at the sampling site, separating sediment and water, and extracting organic compounds from sediment. The largest concentrations of several dissolved herbicides were detected after application on agricultural areas in the spring and early summer in both wet and dry periods. However, dissolved atrazine concentrations also increased in the winter during periods of high streamflow resulting from snow melt. The maximum concentration of dissolved herbicides detected at all sampling sites during the study were: alachlor, 21 micrograms per liter; atrazine, 16 micrograms per liter; cyanazine, 8.7 micrograms per liter; metolachlor, 11.0 micrograms per liter; and metribuzin, 3.0 micrograms per liter. Herbicides can be transported from agricultural areas to the river by overland flow, drainage from agricultural areas conveyed by tile drains, and ground water. Hydrograph separation for 10 locations in the Cedar River basin indicates that the ground-water contribution varies within the basin and probably ranges from 56 to 80 percent of the annual river discharge. The predominance of ground-water contribution, the persistent detection of dissolved atrazine even during base flow, and the variety of dissolved herbicides detected in the river during the dry spring of 1985 indicate that some herbicides are being transported to the river by ground water. Atrazine transported to the Cedar River was estimated to be about 1.4 to 4.0 percent of that applied, depending on the assumed application rate. The large river discharge in June 1984, which was predominantly overland flow, contained about 70 percent of the atrazine transported to the river during 1984.

Iowa, Minnesota↗
USGS1978

Water chemistry of the Redwood Creek and Mill Creek basins, Redwood National Park, Humboldt and Del Norte Counties, California

A 2-year study was made in the Redwood Creek and Mill Creek drainage basins of Redwood National Park to determine existing chemical water-quality conditions and to identify the effects of logging on water quality in the main stems and tributaries of the two basins. Overall, the chemical water quality of the main stems and the tributaries is excellent, suitable for most beneficial uses. Dissolved-solids concentrations range from 25 milligrams per liter in the Redwood Creek basin and 21 milligrams per liter in the Mill Creek basin during the rainy season to 139 and 49 during the dry season. Water shifts from a mixed calcium-sodium bicarbonate-chloride type toward a calcium bicarbonate type from the end of the wet season to the end of the dry season. It shifts back toward a mixed calcium-sodium bicarbonate-chloride type from the end of the dry season to the end of the wet season. The pH shifts with the water type from a median value of 6.80 in the rainy season to 7.37 in the dry season. Nitrogen and phosphorus concentrations are generally too low to support nuisance algae but are high enough, in some streams, to support modest populations, particularly in the main stem where light levels are high. Trace-metal concentrations are low, typical of clean streams. Evidence suggests that dissolved calcium and bicarbonate in stream water is produced by weathering of the Franciscan assemblage underlying the basins but that chlorides are transported inland from the ocean as dry fallout and spray and in rain. Exposure of the surface soils to the elements, either by logging or by natural causes such as sparse vegetation, seems to accelerate weathering, which leads to a calcium bicarbonate water type. Logging accelerates weathering most in the tributary watersheds with regoliths derived from sandstone and least in those with regoliths derived from schist; however, the data suggest that the rate of weathering in a schistose watershed can increase dramatically if soil disruption is extensive. Studies during storms indicated that specific conductance and alkalinity were two to three times as likely to decrease at the discharge peak in logged watersheds as in forested ones. This suggests that overland flow containing lower concentrations of soil-derived dissolved solids than flow from other sources is a larger component of peak flow in logged watersheds than in forested watersheds. Comparing a storm in November 1974 to one in February 1975, nitrate concentration increased significantly from November to February in a stream draining a logged watershed and decreased significantly in a stream draining a forested watershed. Then from the rainy season to the dry season, nitrate decreased in both logged and forested watersheds. This pattern suggests that soil nitrate produced by fixation and organic decomposition early in the rainy season tends to wash out of logged watersheds but be taken up in tree growth in forested watersheds. As the dry season progresses, base flow containing little nitrate enters the streams, causing a decrease in nitrate concentration. By contrast, the other plant nutrients--phosphorus, Kjeldahl nitrogen, ammonium, and dissolved organic carbon--all decreased in streams from the November 1974 storm to the February 1975 storm and changed little from the rainy season through the dry season. This pattern suggests that these materials tend to accumulate in the soil during the dry season and be washed out and diluted as the rainy season progresses. Very little reaches the water table due to soil absorption so that little appears in the base flow during the dry season.

California↗
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↗
USGS2008

Hydrochemical Regions of the Glacial Aquifer System, Northern United States, and Their Environmental and Water-Quality Characteristics

The glacial aquifer system in the United States is a large (953,000 square miles) regional aquifer system of heterogeneous composition. As described in this report, the glacial aquifer system includes all unconsolidated geologic material above bedrock that lies on or north of the line of maximum glacial advance within the United States. Examining ground-water quality on a regional scale indicates that variations in the concentrations of major and minor ions and some trace elements most likely are the result of natural variations in the geologic and physical environment. Study of the glacial aquifer system was designed around a regional framework based on the assumption that two primary characteristics of the aquifer system can affect water quality: intrinsic susceptibility (hydraulic properties) and vulnerability (geochemical properties). The hydrochemical regions described in this report were developed to identify and explain regional spatial variations in ground-water quality in the glacial aquifer system within the hypothetical framework context. Data analyzed for this study were collected from 1991 to 2003 at 1,716 wells open to the glacial aquifer system. Cluster analysis was used to group wells with similar ground-water concentrations of calcium, chloride, fluoride, magnesium, potassium, sodium, sulfate, and bicarbonate into five unique groups. Maximum Likelihood Classification was used to make the extrapolation from clustered groups of wells, defined by points, to areas of similar water quality (hydrochemical regions) defined in a geospatial model. Spatial data that represented average annual precipitation, average annual temperature, land use, land-surface slope, vertical soil permeability, average soil clay content, texture of surficial deposits, type of surficial deposit, and potential for ground-water recharge were used in the Maximum Likelihood Classification to classify the areas so the characteristics of the hydrochemical regions would resemble the characteristics of the clusters. The result of the Maximum Likelihood Classification is a map showing five hydrochemical regions of the glacial aquifer system. Statistical analysis of ion concentrations (calcium, chloride, fluoride, magnesium, sodium, potassium, sulfate, and bicarbonate) in samples collected from wells completed in the glacial aquifer system illustrates that variations in water quality can be explained, in part, by related environmental characteristics that control the movement of ground water through the aquifer system. A comparison of median concentrations of chemical constituents in ground water among the five hydrochemical regions indicates that ground water in the Midwestern Agricultural Region, the Urban-Influenced Region, and the Western Agriculture and Grassland Region has the highest concentrations of major and minor ions, whereas ground water in the Northern and Great Lakes Forested Region and the Mountain and Coastal Forested Region has the lowest concentrations of these ions. Median concentrations of barium, arsenic, lithium, boron, strontium, and nitrite plus nitrate as nitrogen also are significantly different among the hydrochemical regions.

Scientific Investigations Report↗
USGS2014

Water-quality trends for selected sampling sites in the upper Clark Fork Basin, Montana, water years 1996-2010

A large-scale trend analysis was done on specific conductance, selected trace elements (arsenic, cadmium, copper, iron, lead, manganese, and zinc), and suspended-sediment data for 22 sites in the upper Clark Fork Basin for water years 1996–2010. Trend analysis was conducted by using two parametric methods: a time-series model (TSM) and multiple linear regression on time, streamflow, and season (MLR). Trend results for 1996–2010 indicate moderate to large decreases in flow-adjusted concentrations (FACs) and loads of copper (and other metallic elements) and suspended sediment in Silver Bow Creek upstream from Warm Springs. Deposition of metallic elements and suspended sediment within Warm Springs Ponds substantially reduces the downstream transport of those constituents. However, mobilization of copper and suspended sediment from floodplain tailings and stream banks in the Clark Fork reach from Galen to Deer Lodge is a large source of metallic elements and suspended sediment, which also affects downstream transport of those constituents. Copper and suspended-sediment loads mobilized from within this reach accounted for about 40 and 20 percent, respectively, of the loads for Clark Fork at Turah Bridge (site 20); whereas, streamflow contributed from within this reach only accounted for about 8 percent of the streamflow at Turah Bridge. Minor changes in FACs and loads of copper and suspended sediment are indicated for this reach during 1996–2010. Clark Fork reaches downstream from Deer Lodge are relatively smaller sources of metallic elements than the reach from Galen to Deer Lodge. In general, small decreases in loads and FACs of copper and suspended sediment are indicated for Clark Fork sites downstream from Deer Lodge during 1996–2010. Thus, although large decreases in FACs and loads of copper and suspended sediment are indicated for Silver Bow Creek upstream from Warm Springs, those large decreases are not translated to the more downstream reaches largely because of temporal stationarity in constituent transport relations in the Clark Fork reach from Galen to Deer Lodge. Unlike metallic elements, arsenic (a metalloid element) in streams in the upper Clark Fork Basin typically is mostly in dissolved phase, has less variability in concentrations, and has weaker direct relations with suspended-sediment concentrations and streamflow. Arsenic trend results for 1996–2010 indicate generally moderate decreases in FACs and loads in Silver Bow Creek upstream from Opportunity. In general, small temporal changes in loads and FACs of arsenic are indicated for Silver Bow Creek and Clark Fork reaches downstream from Opportunity during 1996–2010. Contribution of arsenic (from Warm Springs Ponds, the Mill-Willow bypass, and groundwater sources) in the Silver Bow Creek reach from Opportunity to Warm Springs is a relatively large source of arsenic. Arsenic loads originating from within this reach accounted for about 11 percent of the load for Clark Fork at Turah Bridge; whereas, streamflow contributed from within this reach only accounted for about 2 percent of the streamflow at Turah Bridge.

Montana↗
USGS2006

Recent (2003-05) water quality of Barton Springs, Austin, Texas, with emphasis on factors affecting variability

From 2003 to 2005, the U.S. Geological Survey, in cooperation with the Texas Commission on Environmental Quality, collected and analyzed water samples from the four springs (orifices) of Barton Springs in Austin, Texas (Upper, Main, Eliza, and Old Mill Springs), with the objective of characterizing water quality. Barton Springs is the major discharge point for the Barton Springs segment of the Edwards aquifer. A three-pronged sampling approach was used: physicochemical properties (including specific conductance and turbidity) were measured continuously; samples were collected from the four springs routinely every 2 weeks (during August-September 2003) to 3 weeks (during June 2004-June 2005) and analyzed for some or all major ions, nutrients, trace elements, soluble pesticides, and volatile organic compounds; and samples were collected from the four springs at more closely spaced intervals during the 2 weeks following two storms and analyzed for the same suite of constituents. Following the two storms, samples also were collected from five of the six major streams that provide recharge to Barton Springs. Spring discharge during both sample collection periods was above average (60 cubic feet per second or greater). Barton Springs was found to be affected by persistent low concentrations of atrazine (an herbicide), chloroform (a drinking-water disinfection by-product), and tetrachloroethene (a solvent). Increased recharge from the major recharging streams resulted in increased calcium, sulfate, atrazine, simazine, and tetrachloroethene concentrations and decreased concentrations of most other major ions, nitrate, and chloroform at one or more of the springs. These changes in concentration demonstrate the influence of water quality in recharging streams on water quality at the springs even during non-stormflow conditions. The geochemical compositions of the four springs indicate that Upper Spring is more contaminated and is influenced by a contributing flow path that is separate from those leading to other springs under all but stormflow conditions. Main, Eliza, and Old Mill Springs share at least one common flow path that contributes contaminants to the three springs. Old Mill Spring, however, is less affected by anthropogenic contaminants than the other springs and receives a greater component of water from a flow path whose geochemistry is influenced by water from the saline zone of the aquifer. At Main Spring, atrazine, simazine, chloroform, and tetrachloroethene concentrations increased following storms, describing breakthrough curves that peaked 2 days following rainfall; at Upper Spring, atrazine and simazine concentrations described breakthrough curves that peaked 1 day following rainfall. At both Main and Upper Springs, additional anthropogenic compounds were detected following storms. The geochemical response of the springs to recharge indicates that much of the transport occurs through conduits. When there is no flow in the recharging streams, ground water advects from the aquifer matrix into the conduits and is transported to the springs. When there is flow in the streams, recharge through the streambeds directly enters the conduit system and is transported to the springs. Following storms, surface runoff recharges through both interstream recharge features and streambeds, delivering runoff-related contaminants to Barton Springs.

Scientific Investigations Report↗
USGS2002

Quality of shallow ground water in areas of recent residential and commercial development, Wichita, Kansas, 2000

Water samples from 30 randomly distributed monitoring wells in areas of recent residential and commercial development (1960–96), Wichita, Kansas, were collected in 2000 as part of the High Plains Regional Ground-Water Study conducted by the U.S. Geological Survey's National Water-Quality Assessment (NAWQA) Program. The samples were analyzed for about 170 water-quality constituents that included chlorofluorocarbons, physical properties, dissolved solids and major ions, nutrients and dissolved organic carbon, trace elements, pesticide compounds, and volatile organic compounds. The purpose of this report is to provide an assessment of water quality in recharge to shallow ground water underlying areas of recent residential and commercial development and to determine the relation of ground-water quality to overlying urban land use. Analyses of water from the 30 monitoring wells for chlorofluorocarbons were used to estimate apparent dates of recharge. Water from 18 wells with nondegraded and uncontaminated chlorofluorocarbon concentrations had calculated apparent recharge dates that ranged from 1979 to 1990 with an average date of 1986. Water from 14 monitoring wells (47 percent) exceeded the 500-milligrams-per-liter Secondary Maximum Contaminant Level established by the U.S. Environmental Protection Agency for dissolved solids in drinking water. The Secondary Maximum Contaminant Levels of 250 milligrams per liter for chloride and sulfate were exceeded in water from one well. The source of the largest concentrations of dissolved solids and associated ions, such as chloride and sulfate, in shallow ground water in the study area probably is highly mineralized water moving out of the Arkansas River into the adjacent, unconsolidated deposits and mixing with the dominant calcium bicarbonate water in the deposits. Concentrations of most nutrients in water from the sampled wells were small, with the exception of nitrate. Although water from the sampled wells did not have nitrate concentrations larger than the 10-milligram-per-liter Maximum Contaminant Level for drinking water, water from 50 percent of the sampled wells showed nitrate enrichment (concentrations greater than 2.0 milligrams per liter). Most trace elements in water from the sampled wells were detected only in small concentrations, and few exceeded respective water-quality standards. Twenty percent of iron concentrations, 40 percent of manganese concentrations, 3 percent of arsenic concentrations, and 13 percent of uranium concentrations exceeded respective Maximum Contaminant Levels or Secondary Maximum Contaminant Levels. A total of 47 pesticide compounds were analyzed in ground-water samples during this study. Water from 73 percent of the wells sampled had detectable concentrations of one or more of 8 of these 47 compounds. The herbicide atrazine or its degradation product deethylatrazine were detected most frequently (in water from 70 percent of the sampled wells). Metolachlor was detected in water from 10 percent of the wells, and simazine was detected in water from 30 percent of the wells sampled. Other pesticides detected included dieldrin, pendimethalin, prometon, and tebuthiuron (each in water from 3 percent of the wells). All concentrations of these compounds were less than established Maximum Contaminant Levels. A total of 85 volatile organic compounds (VOCs) were analyzed in ground-water samples during this study. Water from 43 percent of the wells had a detectable concentration of one or more VOCs. Chloroform was the most frequently detected VOC (23 percent of the wells sampled).Seven other VOCs were detected in water at frequencies of 13 percent or less in the wells sampled. Concentrations of VOCs were less than respective Maximum Contaminant Levels, except one sample with a concentration of 9.0 micrograms per liter for tetrachloroethylene (Maximum Contaminant Level of 5.0 micrograms per liter). An analysis of hydraulic gradient, flow velocity, and residence time of the ground water indicated potential recharge areas that ranged from 0.8 to 2.8 miles upgradient of monitoring-well locations. Nineteen (63 percent) of these potential recharge areas were in agricultural areas or areas in transition from agricultural to residential and (or) commercial land use at the time water sampled from the monitoring wells was recharged to the shallow ground water. The occurrence of atrazine or deethylatrazine in water from 70 percent of the monitoring wells may indicate a historical agricultural land-use relation. This agricultural relation also may affect concentrations of other water-quality constituents of possible agricultural origin such as nitrate, which generally were in excess of background concentrations in shallow ground water.

Kansas↗
USGS2003

Framework for a ground-water quality monitoring and assessment program for California

The State of California uses more ground water than any other State in the Nation. With a population of over 30 million people, an agricultural economy based on intensive irrigation, large urban industrial areas, and naturally elevated concentrations of some trace elements, there is a wide range of contaminant sources that have the potential to contaminate ground water and limit its beneficial uses. In response to the many-and different-potential sources of ground-water contamination, the State of California has evolved an extensive set of rules and programs to protect ground-water quality, and agencies to implement the rules and programs. These programs have in common a focus on compliance with regulations governing chemical use and (or) ground-water quality. Although appropriate for, and successful at, their specific missions, these programs do not at present provide a comprehensive view of ground-water quality in the State of California. In October 2001, The California Assembly passed a bill, AB 599, establishing the Ground-Water- Quality Monitoring Act of 2001.' The goal of AB 599 is to improve Statewide comprehensive ground-water monitoring and increase availability of information about ground-water quality to the public. AB 599 requires the State Water Resources Control Board (SWRCB), in collaboration with an interagency task force (ITF) and a public advisory committee (PAC), to develop a plan for a comprehensive ground-water monitoring program. AB 599 specifies that the comprehensive program should be capable of assessing each ground-water basin in the State through direct and other statistically reliable sampling approaches, and that the program should integrate existing monitoring programs and design new program elements, as necessary. AB 599 also stresses the importance of prioritizing ground-water basins that provide drinking water. The United States Geological Survey (USGS), in cooperation with the SWRCB, and in coordination with the ITF and PAC, has developed a framework for a comprehensive ground-water-quality monitoring and assessment program for California. The proposed framework relies extensively on previous work conducted by the USGS through its National Water-Quality Assessment (NAWQA) program. In particular, the NAWQA program defines three types of ground-water assessment: (1) status, the assessment of the current quality of the ground-water resource; (2) trends, the detection of changes in water quality, and (3) understanding, assessing the human and natural factors that affect ground-water quality. A Statewide, comprehensive ground-water quality-monitoring and assessment program is most efficiently accomplished by applying uniform and consistent study-design and data-collection protocols to the entire State. At the same time, a comprehensive program should be relevant at a variety of scales, and therefore needs to retain flexibility to address regional and local issues. Consequently, many of the program components include a predominant element that will be consistently applied in all basins, and a secondary element that may be applied in specific basins where local conditions warrant attention.

Water-Resources Investigations Report↗
USGS2012

Groundwater levels and water-quality observations pertaining to the Austin Group, Bexar County, Texas, 2009-11

The U.S. Geological Survey, in cooperation with the San Antonio Water System, examined groundwater-level altitudes (groundwater levels) and water-quality data pertaining to the Austin Group in Bexar County, Texas, during 2009–11. Hydrologic data collected included daily mean groundwater levels collected at seven sites in the study area. Water-quality samples were collected at six sites in the study area and analyzed for major ions, nutrients, trace elements, organic carbon, and stable isotopes. The resulting datasets were examined for similarities between sites as well as similarities to data from the Edwards aquifer in Bexar County, Tex. Similarities in the groundwater levels between sites completed in the Austin Group and site J (State well AY-68-37-203; hereafter referred to as the “Bexar County index well”) which is completed in the Edwards aquifer might be indicative of groundwater interactions between the two hydrologic units as a result of nearby faulting or conduit flow. The groundwater levels measured at the sites in the study area exhibited varying degrees of similarity to the Bexar County index well. Groundwater levels at site A (State well AY-68-36-136) exhibited similar patterns as those at the Bexar County index well, but the hydrographs of groundwater levels were different in shape and magnitude in response to precipitation and groundwater pumping, and at times slightly offset in time. The groundwater level patterns measured at sites C, D, and E (State wells AY-68-29-513, AY-68-29-514, and AY-68-29-512, respectively) were not similar to those measured at the Bexar County index well. Groundwater levels at site F (State well AY-68-29-819) exhibited general similarities as those observed at the Bexar County index well; however, there were several periods of notable groundwater-level drawdowns at site F that were not evident at the Bexar County index well. These drawdowns were likely because of pumping from the well at site F. The groundwater levels at sites H and I (State wells AY-68-37-205 and AY-68-29-932, respectively) exhibited similar patterns as those at the Bexar County index well (coefficient of determination [R 2 ] of 0.99 at both wells), indicating there might be some degree of hydrologic connectivity to the Edwards aquifer. In general, the water-quality data indicated that the samples were representative of a calcium carbonate dominated system. The major ion chemistry and relations between magnesium to calcium molar ratios and 87 Sr/ 86 Sr isotopic ratios of samples collected from sites H and I indicated that the groundwater from these sites was most geochemically similar to groundwater collected from site B (State well AY-68-36-134), which is representative of groundwater in the Edwards aquifer. Of the sites sampled in this study, there appears to be varying hydrologic connectivity between groundwater from wells completed in the Austin Group and the Edwards aquifer.

Texas↗
USGS2015

Characterization of hydrology and water quality of Piceance Creek in the Alkali Flat area, Rio Blanco County, Colorado, March 2012

Previous studies by the U.S. Geological Survey identified Alkali Flat as an area of groundwater upwelling, with increases in concentrations of total dissolved solids, and streamflow loss, but additional study was needed to better characterize these observations. The U.S. Geological Survey, in cooperation with the Bureau of Land Management, White River Field Office, conducted a study to characterize the hydrology and water quality of Piceance Creek in the Alkali Flat area of Rio Blanco County, Colorado. Water-quality samples were collected at five springs on March 27, 2012, to determine field properties, major ions, trace elements, and stable isotopes of water. Major-ion and trace-element chemistry indicated that the springs sampled as part of this study were likely recharged by the bedrock aquifer. Isotopic values for the springs plotted close to that of groundwater from the Parachute Creek Member of the Green River Formation, and the isotopic values from both of these sources are similar to the values for Grand Mesa snow. Based on fluoride, lithium, and strontium concentrations, one spring appeared to have different source water than the other four springs. The spring also had higher concentrations of calcium, magnesium, and sulfate relative to the other four springs. Trace-element and major-ion data indicate that this spring was sourced from the Uinta Formation. It was likely the other four springs were primarily sourced from the lower part of the Parachute Creek Member of the Green River Formation as indicated by low sulfate concentrations and high fluoride, lithium, and boron concentrations. Water-quality samples were collected at 16 surface-water-quality sites on March 14, 2012, to determine field properties, major ions, and trace elements. Sodium was the dominant cation and concentrations increased steadily from upstream to downstream along the study reach. Calcium, magnesium, and potassium concentrations remained relatively stable along the study reach. Strontium concentrations were relatively stable along the study reach, whereas boron and lithium concentrations increased appreciably at site PC22031 and remained elevated to the end of the study reach. Loading profiles were used to further refine areas of spring and groundwater input and streamflow gains and losses. Although there was a minor gain in streamflow from sites PC21543 to PC21816 (58 to 59 cubic feet per second (ft 3 /s) during March 2014), the observed increase in dissolved solids load indicated groundwater contribution to Piceance Creek between these two sites. From sites PC22737 to PC22980, dissolved solids load decreased, which was not observed in concentration profiles and indicated that streamflow loss occurred between these two sites. Barium, boron, lithium, and strontium loads showed similar patterns to that of the major ions along the study reach and indicated similar areas of groundwater gain and loss. Boron and lithium load were not observed to decrease in a similar pattern to that of barium and strontium load which would suggest the contribution to the stream from sources with similar chemistry to that of spring sites PCSP2 through PCSP5. Sodium, chloride, and bicarbonate loads increased and decreased along the study reach in a pattern similar to that of dissolved solids load. A chemical mass balance was used to estimate the amount of groundwater and (or) spring water that contributed to the observed changes in water quality along Piceance Creek. This analysis indicated only 5 percent spring water would need to reach Piceance Creek to result in the observed changes in water quality. Instantaneous streamflow was measured from sites PC20133 to PC23721 during field reconnaissance (February 2012) and during synoptic sampling (March 2012). During both February and March, the study reach from sites PC20133 to PC23721 was a losing reach with net losses that ranged from 0.5 ft 3 /s (February) to 3 ft 3 /s (March). Observed changes in streamflow along the study reach helped to depict interactions between groundwater and surface water in the Alkali Flat area. Water-quality samples were collected at five surface-water sites in December 2010 that were sampled as part of a previous USGS study in 2000. Water-quality data collected during December 2010 showed no appreciable difference from water-quality data collected during December 2000 at the five sites.

Colorado↗
USGS2007

Hydrogeology of the Coconino Plateau and adjacent areas, Coconino and Yavapai Counties, Arizona

Two large, regional ground-water flow systems occur in the Coconino Plateau and adjacent areas: the C aquifer and the Redwall-Muav aquifer. The C aquifer occurs mainly in the eastern and southern parts of the 10,300-square-mile Coconino Plateau study area, and the Redwall-Muav aquifer underlies the entire study area. The C aquifer is a water-table aquifer for most of its occurrence with depths to water that range from a few hundred feet to more than 1,500 feet. In the western part of the Coconino Plateau study area, the C aquifer is dry except for small localized perched water-bearing zones decoupled from the C aquifer to the east. The Redwall-Muav aquifer underlies the C aquifer and ranges from at least 3,000 feet below land surface in the western part of the Coconino Plateau study area to more than 3,200 feet below land surface in the eastern part of the study area. The Redwall-Muav aquifer is a confined aquifer for most of its occurrence with hydraulic heads of several hundred to more than 500 feet above the top of the aquifer in the western part of the study area and more than 2,000 feet above the top of the aquifer in the eastern part of the study area near Flagstaff. In the eastern and northeast parts of the area, the C aquifer and the Redwall-Muav aquifer are in partial hydraulic connection through faults and other fractures. The water discharging from the two aquifers on the Coconino Plateau study area is generally of good quality for most intended uses. Water from sites in the lower Little Colorado River Canyon had high concentrations of most trace elements relative to other springs, rivers, and streams in the study area. Concentrations of barium, arsenic, uranium, and lead, and gross alpha radioactivity were greater than U.S. Environmental Protection Agency Maximum Contaminant Levels for drinking water at some sites. Ground water discharging to most springs, streams, and wells on the Coconino Plateau and in adjacent areas is a calcium magnesium bicarbonate type and has low concentrations of the major dissolved constituents. Ground water discharging from the Redwall-Muav aquifer to springs in the lower Little Colorado River Canyon is a mixture of water from the C aquifer and the Redwall-Muav aquifer and is a sodium chloride type with high concentrations of most major dissolved constituents. Concentrations of sulfate and chloride in ground water discharging from the Redwall-Muav aquifer at springs near the south rim of Grand Canyon increase toward the west. Water samples from the Verde River above Mormon Pocket had higher concentrations of most dissolved constituents than samples from springs that discharge from the Redwall-Muav aquifer at Mormon Pocket and in Sycamore Canyon. Water-chemistry data from C aquifer wells and springs in the Flagstaff area indicate that ground-water ages in the aquifer range from 7,000 years to modern and that samples were a mix of younger and older waters. Ground-water ages for the Redwall-Muav aquifer are estimated to range from 22,600 to 7,500 years, and low tritium values indicate that this water is older than water discharging from the C aquifer. Tritium and carbon-14 results indicate that ground water discharging at most springs and streams is a mixture of young and old ground waters, likely resulting from multiple flow paths and multiple recharge areas. Ground-water withdrawals in the study area increased from about 4,000 acre-feet per year prior to 1975, to about 20,000 acre-feet per year in 2003. About two-thirds of the water withdrawn is from the C aquifer and about one-third is from the Redwall-Muav aquifer. In the study area, most development of the C aquifer has occurred near Flagstaff. Development of the Redwall-Muav aquifer is more extensive in Verde Valley where water-bearing zones of the aquifer are closer to land surface. In recent years, however, development of the Redwall-Muav aquifer in the study area has increased in response to population growth and the atten

Scientific Investigations Report↗
USGS2004

Quality of water from shallow wells in the rice-growing area in southwestern Louisiana, 1999 through 2001

In 1999-2001, the U.S. Geological Survey installed and sampled 27 shallow wells in the rice-growing area in southwestern Louisiana as part of the Acadian-Pontchartrain Study Unit of the National Water-Quality Assessment Program. The purpose of this report is to describe the waulity of water from shallow wells in the rice-growing area and to relate that water quality to natural and anthropogenic activities, particularly rice agriculture. Ground-water samples were analyzed for general ground-water properties and about 150 water-quality constituents, including major inorganic ions, trace elements, nutrients, dissolved organic carbon (DOC), pesticides, radon, chloroflourocarbons, and selected stable isotopes. Dissolved solids concentrations for 17 wells exceeded the U.S. Environmental Protection Agency secondary minimum containment level of 500 milligrams per liter (mg/L) for drinking water. Concentrations for major pesticides generally were less than the maximum contaminant levels for drinking water. Two major inorganic ions, sulfate and chloride, and two trace elements, iron and manganese, had concentrations that were greater than the secondary maximum containment levels. Three nutrient concentrations were greater than 2 mg/L, a level that might indicate contamination from human activities, and one nutrient concentration (that for nitrite plus nitrite as nitrogen) was greater than the maximum contaminant level of 10 mg/L for drinking water. The median concentration for DOC was 0.5 mg/L, indicating naturally-occurring DOC conditions in the study area. Thirteen pesticides and 7 pesticide degradation products were detected in 14 of the 27 wells sampled. Bentazon, 2, 4-D, and molinate (three rice herbicides) were detected in water from four, one, and one wells, respectively, and malathion (a rice insecticide) was deteced in water fromone well. Low-level concentrations and few detections of nutrients and pesticides indicated that ground-water quality was affected slightly by anthropogenic activities. Quality-control samples, including field blanks, replicates, and spikes, indicated no bias in ground-water data from collection on analysis. Radon concentrations for 22 of the 24 wells sampled wer at or greater than the U.S. Environmental Protection Agency proposed maximum contaminant level of 300 picocuries per liter. Chlorofluorocarbon concentrations in selected wells indicated the apparent ages of the ground water varied with depth water level and ranged from about 17 to 49 years. The stable isotopes of hydrogen and oxygen in water molecules indicated the origin of ground water in the study area was rainwater that originated near the study area and that few geochemical or physical processes influenced the stable isotopic composition of the shallow ground water. The Spearman rank correlation was used to detemrine whther significant correlations existed between physical properties, selected chemical constituents, the number of pesticides detected, and the apparent age of water. The depth to ground water was positively correlated to the well depth and inversely correlated to dissolved solids and other constituents, such as radon, indicating the ground water was under unconfined or semiconfined conditions and more dilute with increasing depth. As the depth to ground water increased, the concentrations of dissolved solids and other constituents decreased, possibly because the deeper sands had a greater transmittal of ground water, which, over time, would flush out, or dilute, the concentrations of dissolved solids in the natural sediments. The apparent age of water was correlated inversely with nitrite plus nitrite concentration, indicating that as apparent age increased, the nitrite plus nitrite concentration decreased. No significant correlations existed between the number of pesticides detected and any of the physical or chemica

Water-Resources Investigations Report↗