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Data from 5,594 samples collected from 1931 through 2006 were used to describe naturally occurring fluoride concentrations in freshwater aquifers in Louisiana. Statistical analyses were used to summarize fluoride concentrations in the aquifers.
The U.S. Geological Survey (USGS), in cooperation with Texas Tech University, constructed a dataset of selected reservoir storage (daily and instantaneous values), reservoir elevation (daily and instantaneous values), and water-quality data from 59 reservoirs throughout Texas. The period of record for the data is as large as January 1965-January 2010. Data were acquired from existing databases, spreadsheets, delimited text files, and hard-copy reports. The goal was to obtain as much data as possible; therefore, no data acquisition restrictions specifying a particular time window were used. Primary data sources include the USGS National Water Information System, the Texas Commission on Environmental Quality Surface Water-Quality Management Information System, and the Texas Water Development Board monthly Texas Water Condition Reports. Additional water-quality data for six reservoirs were obtained from USGS Texas Annual Water Data Reports. Data were combined from the multiple sources to create as complete a set of properties and constituents as the disparate databases allowed. By devising a unique per-reservoir short name to represent all sites on a reservoir regardless of their source, all sampling sites at a reservoir were spatially pooled by reservoir and temporally combined by date. Reservoir selection was based on various criteria including the availability of water-quality properties and constituents that might affect the trophic status of the reservoir and could also be important for understanding possible effects of climate change in the future. Other considerations in the selection of reservoirs included the general reservoir-specific period of record, the availability of concurrent reservoir storage or elevation data to match with water-quality data, and the availability of sample depth measurements. Additional separate selection criteria included historic information pertaining to blooms of golden algae. Physical properties and constituents were water temperature, reservoir storage, reservoir elevation, specific conductance, dissolved oxygen, pH, unfiltered salinity, unfiltered total nitrogen, filtered total nitrogen, unfiltered nitrate plus nitrite, unfiltered phosphorus, filtered phosphorus, unfiltered carbon, carbon in suspended sediment, total hardness, unfiltered noncarbonate hardness, filtered noncarbonate hardness, unfiltered calcium, filtered calcium, unfiltered magnesium, filtered magnesium, unfiltered sodium, filtered sodium, unfiltered potassium, filtered potassium, filtered chloride, filtered sulfate, unfiltered fluoride, and filtered fluoride. When possible, USGS and Texas Commission on Environmental Quality water-quality properties and constituents were matched using the database parameter codes for individual physical properties and constituents, descriptions of each physical property or constituent, and their reporting units. This report presents a collection of delimited text files of source-aggregated, spatially pooled, depth-dependent, instantaneous water-quality data as well as instantaneous, daily, and monthly storage and elevation reservoir data.
Water analyses are reported for 259 samples collected from the Red River, New Mexico, and its tributaries during low-flow(2001) and spring snowmelt (2002) tracer studies. Water samples were collected along a 20-kilometer reach of the Red River beginning just east of the town of Red River and ending at the U.S. Geological Survey streamflow-gaging station located east of Questa, New Mexico. The study area was divided into three sections where separate injections and synoptic sampling events were performed during the low-flow tracer study. During the spring snowmelt tracer study, three tracer injections and synoptic sampling events were performed bracketing the areas with the greatest metal loading into the Red River as determined from the low-flow tracer study. The lowflow tracer synoptic sampling events were August 17, 20, and 24, 2001. The synoptic sampling events for the spring snowmelt tracer were March 30, 31, and April 1, 2002. Stream and large inflow water samples were sampled using equal-width and depth-integrated sampling methods and composited into half-gallon bottles. Grab water samples were collected from smaller inflows. Stream temperatures were measured at the time of sample collection. Samples were transported to a nearby central processing location where pH and specific conductance were measured and the samples processed for chemical analyses. Cations, trace metals, iron redox species, and fluoride were analyzed at the U.S. Geological Survey laboratory in Boulder, Colorado. Cations and trace metal concentrations were determined using inductively coupled plasma-optical emission spectrometry and graphite furnace atomic absorption spectrometry. Arsenic concentrations were determined using hydride generation atomic absorption spectrometry, iron redox species were measured using ultraviolet-visible spectrometry, and fluoride concentrations were determined using an ion-selective electrode. Alkalinity was measured by automated titration, and sulfate, chloride, and bromide were analyzed by ion chromatography at the U.S. Geological Survey laboratory in Salt Lake City, Utah.
In 2001, the U.S. Geological Survey National Water-Quality Assessment Program collected water samples from 48 wells in the southern High Plains as part of a larger scientific effort to broadly characterize and understand factors affecting water quality of the High Plains aquifer across the entire High Plains. Water samples were collected primarily from domestic wells in Texas and eastern New Mexico. Depths of wells sampled ranged from 100 to 500 feet, with a median depth of 201 feet. Depths to water ranged from 34 to 445 feet below land surface, with a median depth of 134 feet. Of 240 properties or constituents measured or analyzed, 10 exceeded U.S. Environmental Protection Agency public drinking-water standards or guidelines in one or more samples - arsenic, boron, chloride, dissolved solids, fluoride, manganese, nitrate, radon, strontium, and sulfate. Measured dissolved solids concentrations in 29 samples were larger than the public drinking-water guideline of 500 milligrams per liter. Fluoride concentrations in 16 samples, mostly in the southern part of the study area, were larger than the public drinking-water standard of 4 milligrams per liter. Nitrate was detected in all samples, and concentrations in six samples were larger than the public drinking-water standard of 10 milligrams per liter. Arsenic concentrations in 14 samples in the southern part of the study area were larger than the new (2002) public drinking-water standard of 10 micrograms per liter. Radon concentrations in 36 samples were larger than a proposed public drinking-water standard of 300 picocuries per liter. Pesticides were detected at very small concentrations, less than 1 microgram per liter, in less than 20 percent of the samples. The most frequently detected compounds were atrazine and breakdown products of atrazine, a finding similar to those of National Water-Quality Assessment aquifer studies across the Nation. Four volatile organic compounds were detected at small concentrations in six water samples. About 70 percent of the 48 primarily domestic wells sampled contained some fraction of recently (less than about 50 years ago) recharged ground water, as indicated by the presence of one or more pesticides, or tritium or nitrate concentrations greater than threshold levels.
Chester County encompasses 760 square miles in southeastern Pennsylvania. Groundwater-quality studies have been conducted in the county over several decades to address specific hydrologic issues. This report compiles and describes water-quality data collected during studies conducted mostly after 1990 and summarizes the data in a county-wide perspective. In this report, water-quality constituents are described in regard to what they are, why the constituents are important, and where constituent concentrations vary relative to geology or land use. Water-quality constituents are grouped into logical units to aid presentation: water-quality constituents measured in the field (pH, alkalinity, specific conductance, and dissolved oxygen), common ions, metals, radionuclides, bacteria, nutrients, pesticides, and volatile organic compounds. Water-quality constituents measured in the field, common ions (except chloride), metals, and radionuclides are discussed relative to geology. Bacteria, nutrients, pesticides, and volatile organic compounds are discussed relative to land use. If the U.S. Environmental Protection Agency (USEPA) or Chester County Health Department has drinking water standards for a constituent, the standards are included. Tables and maps are included to assist Chester County residents in understanding the water-quality constituents and their distribution in the county. Ground water in Chester County generally is of good quality and is mostly acidic except in the carbonate rocks and serpentinite, where it is neutral to strongly basic. Calcium carbonate and magnesium carbonate are major constituents of these rocks. Both compounds have high solubility, and, as such, both are major contributors to elevated pH, alkalinity, specific conductance, and the common ions. Elevated pH and alkalinity in carbonate rocks and serpentinite can indicate a potential for scaling in water heaters and household plumbing. Low pH and low alkalinity in the schist, quartzite, and gneiss rocks can indicate a potential for corrosive water. The only constituent measured in the field that has a USEPA Secondary Maximum Contaminant Level (SMCL) is pH. The SMCL for pH is 6.5-8.5; 64 percent of samples analyzed for pH were acidic (below pH 6.5). Only 1 percent of samples were basic (above pH 8.5). Of the common ions, the USEPA has SMCLs for chloride, sulfate, and total dissolved solids. The USEPA has a SMCL and a Primary Maximum Contaminant Level (PMCL) for fluoride. Chloride is more closely related to land use than geology. In Chester County, chloride exceeded the SMCL (250 mg/L) only in 5 percent of the services (commercial services, community services, and military) land-use areas. No samples analyzed for sulfate exceeded the SMCL (250 mg/L). Only 3 percent of samples analyzed for total dissolved solids exceeded the SMCL (500 milligrams per liter) (mg/L). No samples analyzed for fluoride equaled or exceeded the SMCL (2.0 mg/L) or PMCL (4.0 mg/L). Iron concentrations exceeded the USEPA SMCL in 11 percent of samples and were highest in schist (14 percent) and gneiss (13 percent). Manganese concentrations exceeded the SMCL in 19 percent of samples and were highest in quartzite and schist (both 28 percent). Lead and arsenic were present in low concentrations: the highest concentrations of lead occurred in water from quartzite (8 percent exceeded the USEPA Action Level), and arsenic was detected mostly in Triassic sedimentary rocks (9 percent exceeded the USEPA PMCL). The highest concentrations of copper occurred more frequently in quartzite rocks, and to a lesser extent were evenly distributed between ground water in gneiss, schist, and Triassic sedimentary rocks. Elevated concentrations of radon-222 and the combined radium-226/radium-228 radionuclides were common in water from quartzite and schist. Gross alpha and gross beta particle activities were elevated in water from quartzite and carbonate rocks. In contrast, elevated concentrations of uranium primarily were measured in water from Triassic sedimentary and carbonate rocks. Despite a sampling bias towards agricultural land use, only two samples indicated the presence of fecal coliforms. Samples analyzed for nutrients generally exhibited low concentrations, but about 11 percent of samples collected for nitrate exceeded the USEPA PMCL. Only one nitrite sample (less than 1 percent) exceeded the respective USEPA PMCL. Approximately 190 samples were collected for each of the three pesticides in this report: lindane, dieldrin, and diazinon. Sampling was biased towards agricultural, low-medium density residential, and wooded land uses. Approximately 95 percent of samples for each pesticide were below minimum reporting levels (MRL). Only lindane has a USEPA PMCL, and only one sample exceeded the standard. Results for dieldrin and diazinon were similar, except results for two diazinon samples where concentrations were 57.0 and 490 micrograms per liter (μg/L). Volatile organic compounds in this report were analyzed in water from 198 samples. Sampling was biased towards agricultural, low-medium density residential, and wooded land uses. Two percent of samples analyzed for trichloroethylene and less than 1 percent of samples analyzed for tetrachloroethylene exceeded their respective USEPA PMCLs (each 5.0 μg/L). No samples analyzed for 1,1,1-trichloroethane exceeded the USEPA PMCL (200 μg/L). No samples analyzed for methyl tert-butyl ether exceeded the USEPA Drinking Water Advisory (20μg/L).
Water analyses are reported for 104 samples collected from numerous thermal and non-thermal features in Yellowstone National Park (YNP) during 2006-2008. Water samples were collected and analyzed for major and trace constituents from 10 areas of YNP including Apollinaris Spring and Nymphy Creek along the Norris-Mammoth corridor, Beryl Spring in Gibbon Canyon, Norris Geyser Basin, Lower Geyser Basin, Crater Hills, the Geyser Springs Group, Nez Perce Creek, Rabbit Creek, the Mud Volcano area, and Washburn Hot Springs. These water samples were collected and analyzed as part of research investigations in YNP on arsenic, antimony, iron, nitrogen, and sulfur redox species in hot springs and overflow drainages, and the occurrence and distribution of dissolved mercury. Most samples were analyzed for major cations and anions, trace metals, redox species of antimony, arsenic, iron, nitrogen, and sulfur, and isotopes of hydrogen and oxygen. Analyses were performed at the sampling site, in an on-site mobile laboratory vehicle, or later in a U.S. Geological Survey laboratory, depending on stability of the constituent and whether it could be preserved effectively. Water samples were filtered and preserved on-site. Water temperature, specific conductance, pH, emf (electromotive force or electrical potential), and dissolved hydrogen sulfide were measured on-site at the time of sampling. Dissolved hydrogen sulfide was measured a few to several hours after sample collection by ion-specific electrode on samples preserved on-site. Acidity was determined by titration, usually within a few days of sample collection. Alkalinity was determined by titration within 1 to 2 weeks of sample collection. Concentrations of thiosulfate and polythionate were determined as soon as possible (generally a few to several hours after sample collection) by ion chromatography in an on-site mobile laboratory vehicle. Total dissolved iron and ferrous iron concentrations often were measured on-site in the mobile laboratory vehicle. Concentrations of dissolved aluminum, arsenic, boron, barium, beryllium, calcium, cadmium, cobalt, chromium, copper, iron, potassium, lithium, magnesium, manganese, molybdenum, sodium, nickel, lead, selenium, silica, strontium, vanadium, and zinc were determined by inductively coupled plasma-optical emission spectrometry. Trace concentrations of dissolved antimony, cadmium, cobalt, chromium, copper, lead, and selenium were determined by Zeeman-corrected graphite-furnace atomic-absorption spectrometry. Dissolved concentrations of total arsenic, arsenite, total antimony, and antimonite were determined by hydride generation atomic-absorption spectrometry using a flow-injection analysis system. Dissolved concentrations of total mercury and methylmercury were determined by cold-vapor atomic fluorescence spectrometry. Concentrations of dissolved chloride, fluoride, nitrate, bromide, and sulfate were determined by ion chromatography. For many samples, concentrations of dissolved fluoride also were determined by ion-specific electrode. Concentrations of dissolved ferrous and total iron were determined by the FerroZine colorimetric method. Concentrations of dissolved ammonium were determined by ion chromatography, with reanalysis by colorimetry when separation of sodium and ammonia peaks was poor. Dissolved organic carbon concentrations were determined by the wet persulfate oxidation method. Hydrogen and oxygen isotope ratios were determined using the hydrogen and CO 2 equilibration techniques, respectively.
This annual report describes studies by the U. S. Geological Survey, sponsored by the U. S. Atomic Energy Commission, to determine the hydrologic effects of disposal of radioactive waste to the ground at the National Reactor Testing Station. The project has involved the collection and analyses of ground-and surface-water samples for radiometric and chemical changes. Results have been evaluated and mapped. Ground-water levels have also been mapped over the station. The net ground-water consumption after pumpage and waste injection has been determined. Two billion gallons of water were pumped during 1966 of which 40 percent was metered and returned to the Snake Plain aquifer. A record runoff of the Big Lost River during 1965 and 1966 induced a large amount of recharge to the Snake Plain aquifer. The recharge caused water levels to rise as much as six feet, but apparently did not have a great effect on the concentrations of waste products in the ground water. Pressure transmission, or mass transfer effects from the recharge, were observed as far as 50 miles southwest of the river. Tritium is the primary radioactive waste product discharged to the subsurface. Several aspects of tritium disposal have been studied in detail at the TRA (Test Reactor Area) and the ICPP (Idaho Chemical Processing Plant) areas. The distribution of waste tritium in the Snake Plain aquifer has been mapped, and background levels were determined to range from 0.05 to 0.1 pCi/m1 (picocuries per milliliter). Waste tritium in water from the Snake Plain aquifer has been detected 4-1/2 miles south of the ICPP. An estimated mass balance of total tritium remaining in the Snake Plain aquifer is presented for the TRA and ICPP areas. About 21,500 Ci (curies) of tritium at the ICPP and about 3,700 Ci at the TRA have been disposed from 1952 through 1966. About 14,000 Ci and 2,700 Ci of tritium, respectively, should remain after radioactive decay. Similar amounts are indicated to be present in the ground water. Waste tritium has been used as a tracer in studies of the complex flow characteristics of the aquifer in the ICPP area. Dissolved chromium has been used to trace TRA pond waste water in perched ground-water bodies and downgradient 2-1/2 miles in the Snake Plain aquifer. Concentrations of hexavalent chromium ranged as high as 1.7 ppm (parts per million) in the perched water and 0.4 ppm in the water from the Snake Plain aquifer. Chromium serves as a good tracer of TRA wastes because it does not occur in nearby ICPP wastes, is not usually present in natural waters, and can be determined in very low concentrations. Natural fluoride in the water of the Snake Plain aquifer has been used to trace the ground-water flow downgradient from the northeast end of the Snake River Plain. The fluoride, which is dissolved from certain rocks, indicates recharge areas and flow paths in the aquifer. A project to test the feasibility of disposing radioactive gases into the ground is presently underway. A seismic survey was used to map surface sediment thickness, and two test wells were cored to evaluate potential injection-well sites. A "breathing" well has been instrumented to study flow rates, temperature, humidity, and other aspects of vertical flow of air in the well. Results of the continuing study are presented. Studies made on several wells which had vertically flowing borehole water indicated that the physical and chemical properties of the water are influenced by the flow. One well with downward flow had a head difference of 0.01 to 0.07 foot between two permeable zones throughout the year.
Data on groundwater quality, hydrogeology, and land and water use for the Carson River basin, Nevada and California were analyzed as part of the U. S. Geological Survey National Water-Quality Assessment program. The basin consists of six hydrographic areas--a mountainous headwaters area and five downstream areas interconnected by the Carson River. Each valley contains one or more basin-fill aquifers. The data on groundwater quality came from several agencies and were screened to verify site location and to avoid analyses of treated water. The screened data are stored in the U. S. Geological Survey National Water Information System data base. Differences in sample-collection and preservation procedures among some of the data-collection agencies restrict use of the data to a descriptive analysis. Drinking water standards were employed as the basis for evaluating reported concentrations. Frequencies with which primary or secondary standards are exceeded increase from upstream parts of the basin to downstream parts. Primary standards commonly exceeded are fluoride in upstream areas and arsenic and fluoride in downstream areas. Secondary standards commonly exceeded are iron and manganese in upstream areas and chloride, dissolved solids, iron, manganese, and sulfate in downstream areas. The poorer-quality groundwater generally is a result of natural geochemical reactions, rather than the introduction of chemicals by man. Limited data indicate, however , that manmade organic compounds are present, mostly at or near urban land.
Washington County occupies an area of 864 square miles in southwestern Pennsylvania and lies within the Pittsburgh Plateaus Section of the Appalachian Plateaus physiographic province. About 69 percent of the county population is served by public water-supply systems, and the Monongahela River is the source for 78 percent of the public-supply systems. The remaining 31 percent of the population depends on wells, springs, and cisterns for its domestic water supply. The sedimentary rocks of Pennsylvanian and Permian age that underlie the county include sandstone, siltstone, limestone, shale, and coal. The mean reported yield of bedrock wells ranges from 8.8 gallons per minute in the Pittsburgh .Formation to 46 gallons per minute in the Casselman Formation. Annual water-level fluctuations usually range from less than 3 ft (feet) beneath a valley to about 16 ft beneath a hilltop. Average hydraulic conductivity ranges from 0.01 to 18 ft per day. Water-level fluctuations and aquifer-test results suggest that most ground water circulates within 150 ft of land surface. A three-dimensional computer flow-model analysis indicates 96 percent of the total ground-water recharge remains in the upper 80 to 110 ft of bedrock (shallow aquifer system). The regional flow system (more than 250ft deep in the main valley) receives less than 0.1 percent of the total ground-water recharge from the Brush Run basin. The predominance of the shallow aquifer system is substantiated by driller's reports, which show almost all water bearing zones are less than 150ft below land surface. The modeling of an unmined basin showed that the hydrologic factors that govern regional groundwater flow can differ widely spatially but have little effect on the shallow aquifers that supply water to most domestic wells. However, the shallow aquifers are sensitive to hydrologic factors within this shallow aquifer system (such as ground-water recharge, hydraulic conductivity of the streamaquifer interface, and hydraulic conductivity of the aquifer). A vertical fracture zone would probably increase ground-water availability within the zone and would probably result in a lower head in the shallow aquifers in an upland draw area and an increased head in a valley. l Streams in the northern and western parts of the county drain to the Ohio River and streams in the eastern and southern parts of the county drain to the Monongahela River. The computed 7-day, 10-year low-flow frequencies for the surface-water sites ranged from 0.0 to 55 x 10-3 cubic feet per second per square mile. The lowest low-flow discharges per square mile were in the south-central and southwestern parts of the county. The highest low-flow discharges per square mile were in the eastern and northern parts of the county. The annual water loss at five gaged streams ranged from 52 to 75 percent of the total precipitation. The loss resulted from evaporation, transpiration, diversion, mines, ground-water outflow from the system, and plant and animal consumption. The major ground-water-quality problems are elevated concentrations of iron, manganese, and dissolved solids, and very hard water. Minor groundwater-quality problems include elevated concentrations of fluoride, chloride, and sulfate. Downgradient along the ground-water flow path, principal ions change from mostly calcium, magnesium, sulfate, and bicarbonate to sodium and chloride. Dissolyed-solids concentrations generally increase with residence time .. Elevated concentrations of sulfate and total dissolved solids were common at the surface-water sites in the northern and eastern parts of the county where most of the active and abandohed coal mines are located and where acid mine drainage is most prevalent. However, measured alkalinity at most of the surface-water sites ranged from 86 to 345 milligrams per liter, indicating that these streams would have a neutralizing effect on most inflows of acid mine drainage. The model of the hypothetically mined Brush Run basin shows that the vertical hydraulic conductivity (either existing or induced by mine subsidence) between the shallow ground-water system and the mine, and the depth to the mine are critical controls on the amount of ground water entering the mine. When the vertical hydraulic conductivity was increased by a factor of four for a mine about 250 ft deep in the main valley, inflow to the mine increased almost by the same factor. The model also shows that increasing the depth to a mine by 200 ft (mine about 450 ft deep in main valley) would cause mine inflow to decrease one order of magnitude. Comparisons between stream discharges during low base-flow conditions in a mined basin (Daniels Run) and an unrnined basin (Brush Run) indicated that the deep mining did not substantially lower streamflow. Although streamflow decreased and, at times, completely disappeared in the middle and lower parts of Daniels Run basin, it reappeared again downstream as ground-water discharge and was part of the flow at the mouth of Daniels Run. Comparison of the water-quality characteristics of the two basins showed that concentrations of dissolved solids, sulfate, sodium, chloride, fluoride, and manganese were greater in the mined basin than in the unmined basin. The pH and iron concentrations were similar in both basins.
The U.S. Geological Survey, in cooperation with the New Mexico Environment Department, is investigating the pre-mining ground-water chemistry at the Molycorp molybdenum mine in the Red River Valley, New Mexico. The primary approach is to determine the processes controlling ground-water chemistry at an unmined, off-site but proximal analog. The Straight Creek catchment, chosen for this purpose, consists of the same Tertiary-age quartz-sericite-pyrite altered andesite and rhyolitic volcanics as the mine site. Straight Creek is about 5 kilometers east of the eastern boundary of the mine site. Both Straight Creek and the mine site are at approximately the same altitude, face south, and have the same climatic conditions. Thirteen wells in the proximal analog drainage catchment were sampled for ground-water chemistry. Eleven wells were installed for this study and two existing wells at the Advanced Waste-Water Treatment (AWWT) facility were included in this study. Eight wells were sampled outside the Straight Creek catchment: one each in the Hansen, Hottentot, and La Bobita debris fans, four in a well cluster in upper Capulin Canyon (three in alluvial deposits and one in bedrock), and an existing well at the U.S. Forest Service Questa Ranger Station in Red River alluvial deposits. Two surface waters from the Hansen Creek catchment and two from the Hottentot drainage catchment also were sampled for comparison to ground-water compositions. In this report, these samples are evaluated to determine if the geochemical interpretations from the Straight Creek ground-water geochemistry could be extended to other ground waters in the Red River Valley , including the mine site. Total-recoverable major cations and trace metals and dissolved major cations, selected trace metals, anions, alkalinity; and iron-redox species were determined for all surface- and ground-water samples. Rare-earth elements and low-level As, Bi, Mo, Rb, Re, Sb, Se, Te, Th, U, Tl, V, W, Y, and Zr were determined on selected samples. Dissolved organic carbon (DOC), mercury, sulfate stable isotope composition (δ 34 S and δ 18 O of sulfate), stable isotope composition of water (δ 2 H and δ 18 O of water) were measured for selected samples. Chlorofluorocarbons (CFC) and 3 He and 3 H were measured for age dating on selected samples. Linear regressions from the Straight Creek ground-water data were used to compare ground-water chemistry trends in non-Straight Creek ground waters with Straight Creek alluvial ground-water chemistry dilution trends. Most of the solute trends for the ground waters are similar to those for Straight Creek but there are some notable exceptions. In lithologies that contain substantial pyrite mineralization, acid waters form with similar chemistries to those in Straight Creek and all the waters tend to be calcium-sulfate type. Hottentot ground waters contain substantially lower calcium concentrations relative to those in Straight Creek. This anomaly results from the exposure of rhyolite porphyry in the Hottentot scar and weathering zone. The rhyolite contains less calcium than the altered andesites and tuffs in the Straight Creek catchment and probably does not have the abundant gypsum and calcite. The Hansen ground waters have reached gypsum saturation and have similar calcium, magnesium, and beryllium concentrations as Straight Creek ground waters but have lower concentrations of fluoride, manganese, zinc, cobalt, nickel, copper, and lithium. Lower concentrations of elements related to mineralization at Hansen likely reflect the more distal location of Hansen with respect to intrusive centers that provided the heat source for hydrothermal alteration. The other ground water with water chemistry trends that are outside the Straight Creek trends was from an alluvial well from Capulin Canyon (CC2A). Although it had pH values near 6.0 and most major ions similar to the other Capulin Canyon ground waters, it contained high concentrations of fluoride, manganese, aluminum, iron, beryllium, and zinc similar to a mineralized zone and had low alkalinity. Saturation indices indicate that solubility constraints continue to provide upper limits on some solute concentrations. Siderite, ferrihydrite, calcite, gypsum, rhodochrosite, and barite provide limits for concentrations of Fe(II), Fe(III), Ca, Mn, and Ba, respectively. Beryllium concentrations may be subject to an upper concentration limit by the solubility of Be(OH) 2 but these concentrations probably are not reached in the ground waters. Ground-water isotopic data were consistent with the meteoric water line estimated for precipitation in the Red River Valley, indicating that all the ground waters examined in this study were meteoric, recent in origin, and showed no substantial indication of evaporation. Tritium-helium-3 and chlorofluorocarbon (CFC) age dating were partially successful. Generally, dates were consistent with location and depth of wells. Two samples had good agreement between CFC dates and tritium-helium dates, whereas a third reflected either substantial mixing with younger or older waters or complications arising from excess helium-4. The well at La Bobita appeared to contain a large component of modern water, most likely as a result of mixing with water from Red River alluvial deposits.
To demonstrate the value of long-term, water-quality monitoring, the Michigan Department of Environmental Quality (MDEQ), in cooperation with the U.S. Geological Survey (USGS), initiated a study to evaluate potential trends in water-quality constituents for selected National Stream Quality Accounting Network (NASQAN) stations in Michigan. The goal of this study is to assist the MDEQ in evaluating the effectiveness of water-pollution control efforts and the identification of water-quality concerns. The study included a total of nine NASQAN stations in Michigan. Approximately 28 constituents were analyzed for trend tests. Station selection was based on data availability, land-use characteristics, and station priority for the MDEQ Water Chemistry Monitoring Project. Trend analyses were completed using the uncensored Seasonal Kendall Test in the computer program Estimate Trend (ESTREND), a software program for the detection of trends in water-quality data. The parameters chosen for the trend test had (1) at least a 5-year period of record (2) about 5 percent of the observations censored at a single reporting limit, and (3) 40 percent of the values within the beginning one-fifth and ending one-fifth of the selected period. In this study, a negative trend indicates a decrease in concentration of a particular constituent, which generally means an improvement in water quality; whereas a positive trend means an increase in concentration and possible degradation of water quality. The results of the study show an overall improvement in water quality at the Clinton River at Mount Clemens, Manistee River at Manistee, and Pigeon River near Caseville. The detected trend for these stations show decreases in concentrations of various constituents such as nitrogen compounds, conductance, sulfate, fecal coliform bacteria, and fecal streptococci bacteria. The negative trend may indicate an overall improvement in agricultural practices, municipal and industrial wastewater-treatment processes, and effective regulations. Phosphorus data for most of the study stations could not be analyzed because of the data limitations for trend tests. The only station with a significant negative trend in total phosphorus concentration is the Clinton River at Mount Clemens. However, scatter-plot analyses of phosphorus data indicate decreasing concentrations with time for most of the study stations. Positive trends in concentration of nitrogen compounds were detected at the Kalamazoo River near Saugatuck and Muskegon River near Bridgeton. Positive trends in both fecal coliform and total fecal coliform were detected at the Tahquamenon River near Paradise. Various different point and nonpoint sources could produce such positive trends, but most commonly the increase in concentrations of nitrogen compounds and fecal coliform bacteria are associated with agricultural practices and sewage-plant discharges. The constituent with the most numerous and geographically widespread significant trend is pH. The pH levels increased at six out of nine stations on all the major rivers in Michigan, with no negative trend at any station. The cause of pH increase is difficult to determine, as it could be related to a combination of anthropogenic activities and natural processes occurring simultaneously in the environment. Trends in concentration of major ions, such as calcium, sodium, magnesium, sulfate, fluoride, chloride, and potassium, were detected at eight out of nine stations. A negative trend was detected only in sulfate and fluoride concentrations; a positive trend was detected only in calcium concentration. The major ions with the most widespread significant trends are sodium and chloride; three positive and two negative trends were detected for sodium, and three negative and two positive trends were detected for chloride. The negative trends in chloride concentrations outnumbered the positive trends. This result indicates a slight improvement in surface-water quality because chloride as a point source in natural water comes from deicing salt, sewage effluents, industrial wastes, and oil fields. For other major ions, such as magnesium and potassium, both positive and negative trends were detected. These changes in trends indicate changes in surface-water quality caused by a variety of point and non-point sources throughout Michigan, as well as natural changes in the environment.
In 2000, the U.S. Geological Survey, in cooperation with Park County, Colorado, began a study to evaluate ground-water quality in the various aquifers in Park County that supply water to domestic wells. The focus of this study was to identify and describe the principal natural and human factors that affect ground-water quality. In addition, the potential effects of individual sewage disposal system (ISDS) effluent on ground-water quality were evaluated. Ground-water samples were collected from domestic water-supply wells from July 2001 through October 2004 in the alluvial, crystalline-rock, sedimentary-rock, and volcanic-rock aquifers to assess general ground-water quality and effects of ISDS's on ground-water quality throughout Park County. Samples were analyzed for physical properties, major ions, nutrients, bacteria, and boron; and selected samples also were analyzed for dissolved organic carbon, human-related (wastewater) compounds, trace elements, radionuclides, and age-dating constituents (tritium and chlorofluorocarbons). Drinking-water quality is adequate for domestic use throughout Park County with a few exceptions. Only about 3 percent of wells had concentrations of fluoride, nitrate, and (or) uranium that exceeded U.S. Environmental Protection Agency national, primary drinking-water standards. These primary drinking-water standards were exceeded only in wells completed in the crystalline-rock aquifers in eastern Park County. Escherichia coli bacteria were detected in one well near Guffey, and total coliform bacteria were detected in about 11 percent of wells sampled throughout the county. The highest total coliform concentrations were measured southeast of the city of Jefferson and west of Tarryall Reservoir. Secondary drinking-water standards were exceeded more frequently. About 19 percent of wells had concentrations of one or more constituents (pH, chloride, fluoride, sulfate, and dissolved solids) that exceeded secondary drinking-water standards. Currently (2004), there is no federally enforced drinking-water standard for radon in public water-supply systems, but proposed regulations suggest a maximum contaminant level of 300 picocuries per liter (pCi/L) and an alternative maximum contaminant level of 4,000 pCi/L contingent on other mitigating remedial activities to reduce radon levels in indoor air. Radon concentrations in about 91 percent of ground-water samples were greater than or equal to 300 pCi/L, and about 25 percent had radon concentrations greater than or equal to 4,000 pCi/L. Generally, the highest radon concentrations were measured in samples collected from wells completed in the crystalline-rock aquifers. Analyses of ground-water-quality data indicate that recharge from ISDS effluent has affected some local ground-water systems in Park County. Because roughly 90 percent of domestic water used is assumed to be recharged by ISDS's, detections of human-related (wastewater) compounds in ground water in Park County are not surprising; however, concentrations of constituents associated with ISDS effluent generally are low (concentrations near the laboratory reporting levels). Thirty-eight different organic wastewater compounds were detected in 46 percent of ground-water samples, and the number of compounds detected per sample ranged from 1 to 17 compounds. Samples collected from wells with detections of wastewater compounds also had significantly higher (p-value < 0.05) chloride and boron concentrations than samples from wells with no detections of wastewater compounds. ISDS density (average subdivision lot size used to estimate ISDS density) was related to ground-water quality in Park County. Chloride and boron concentrations were significantly higher in ground-water samples collected from wells located in areas that had average subdivision lot sizes of less than 1 acre than in areas that had average subdivision lot sizes greater than or equal to 1 acre. For wells completed in the crystalline-
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.
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
Because of water quantity and quality concerns within the Ozark aquifer, the State of Kansas in 2004 issued a moratorium on most new appropriations from the aquifer until results were made available from a cooperative study between the U.S. Geological Survey and the Kansas Water Office. The purposes of the study were to develop a regional ground-water flow model and a water-quality assessment of the Ozark aquifer in northwestern Arkansas, southeastern Kansas, southwestern Missouri, and northeastern Oklahoma (study area). In 2006 and 2007, water-quality samples were collected from 40 water-supply wells completed in the Ozark aquifer and spatially distributed throughout the study area. Samples were analyzed for physical properties, dissolved solids and major ions, nutrients, trace elements, and selected isotopes. This report presents the results of the water-quality assessment part of the cooperative study. Water-quality characteristics were evaluated relative to U.S. Environmental Protection Agency drinking-water standards. Secondary Drinking-Water Regulations were exceeded for dissolved solids (11 wells), sulfate and chloride (2 wells each), fluoride (3 wells), iron (4 wells), and manganese (2 wells). Maximum Contaminant Levels were exceeded for turbidity (3 wells) and fluoride (1 well). The Maximum Contaminant Level Goal for lead (0 milligrams per liter) was exceeded in water from 12 wells. Analyses of isotopes in water from wells along two 60-mile long ground-water flow paths indicated that water in the Ozark aquifer was at least 60 years old but the upper age limit is uncertain. The source of recharge water for the wells along the flow paths appeared to be of meteoric origin because of isotopic similarity to the established Global Meteoric Water Line and a global precipitation relation. Additionally, analysis of hydrogen-3 (3H) and carbon-14 (14C) indicated that there was possible leakage of younger ground water into the lower part of the Ozark aquifer. This may be caused by cracks or fissures in the confining unit that separates the upper and lower parts of the aquifer, poorly constructed or abandoned wells, or historic mining activities. Analyses of major ions in water from wells along the flow paths indicated a transition from freshwater in the east to saline water in the west. Generally, ground water along flow paths evolved from a calcium magnesium bicarbonate type to a sodium calcium bicarbonate or a sodium calcium chloride bicarbonate type as water moved from recharge areas in Missouri into Kansas. Much of this evolution occurred within the last 20 to 25 miles of the flow paths along a water-quality transition zone near the Kansas-Missouri State line and west. The water quality of the Kansas part of the Ozark aquifer is degraded compared to the Missouri part. Geophysical and well-bore flow information and depth-dependent water-quality samples were collected from a large-capacity (1,900-2,300 gallons per minute) municipal-supply well to evaluate vertical ground-water flow accretion and variability in water-quality characteristics at different levels. Although the 1,050-foot deep supply well had 500 feet of borehole open to the Ozark aquifer, 77 percent of ground-water flow entering the borehole came from two 20-foot thick rock layers above the 1,000-foot level. For the most part, water-quality characteristics changed little from the deepest sample to the well-head sample, and upwelling of saline water from deeper geologic formations below the well was not evident. However, more saline water may be present below the bottom of the well.
The Marine Corps Air Ground Combat Center (MCAGCC) Twentynine Palms, California, overlies the Surprise Spring, Deadman, Mesquite, and Mainside subbasins of the Morongo groundwater basin in the southern Mojave Desert. Historically, the MCAGCC has relied on groundwater pumped from the Surprise Spring subbasin to provide all of its potable water supply. Groundwater pumpage in the Surprise Spring subbasin has caused groundwater levels in the subbasin to decline by as much as 190 feet (ft) from 1953 through 2007. Groundwater from the other subbasins contains relatively high concentrations of fluoride, arsenic, and (or) dissolved solids, making it unsuitable for potable uses without treatment. The potable groundwater supply in Surprise Spring subbasin is diminishing because of pumping-induced overdraft and because of more restrictive Federal drinking-water standards on arsenic concentrations. The U.S. Geological Survey, in cooperation with the MCAGCC, completed this study to better understand groundwater resources in the area and to help establish a long-term strategy for regional water-resource development. The Surprise Spring, Deadman, Mesquite, and Mainside subbasins are filled with sedimentary deposits of Tertiary age, alluvial fan deposits of Quaternary-Tertiary age, and younger alluvial and playa deposits of Quaternary age. Combined, this sedimentary sequence reaches a maximum thickness of more than 16,000 ft in the Deadman and Mesquite subbasins. The sedimentary deposits of Tertiary age yield a small amount of water to wells, and this water commonly contains high concentrations of fluoride, arsenic, and dissolved solids. The alluvial fan deposits form the principal water-bearing unit in the study area and have a combined thickness of 250 to more than 1,000 ft. The younger alluvial and playa deposits are unsaturated throughout most of the study area. Lithologic and downhole geophysical logs were used to divide the Quaternary/ Tertiary alluvial fan deposits into two aquifers (referred to as the upper and the middle aquifers) and the Tertiary sedimentary deposits into a single aquifer (referred to as the lower aquifer). In general, wells perforated in the upper aquifer yield more water than wells perforated in the middle and lower aquifers. The study area is dominated by extensive faulting and moderate to intense folding that has displaced or deformed the pre-Tertiary basement complex as well as the overlying Tertiary and Quaternary deposits. Many of these faults act as barriers to the lateral movement of groundwater flow and form many of the boundaries of the groundwater subbasins. The principal recharge to the study area is groundwater underflow across the western and southern boundaries that originates as runoff in the surrounding mountains. Groundwater discharges naturally from the study area as spring flow, as groundwater underflow to downstream basins, and as water vapor to the atmosphere by transpiration of phreatophytes and direct evaporation from moist soil. The annual volume of water that naturally recharged to or discharged from the groundwater flow system in the study area during predevelopment conditions was estimated to be 1,010 acre-feet per year (acre-ft/yr). About 90 percent of this recharge originated as runoff from the Little San Bernardino and the Pinto Mountains to the south, and the remainder originated as runoff from the San Bernardino Mountains to the west. Evapotranspiration by phreatophytes near Mesquite Lake (dry) was the primary form of predevelopment groundwater discharge. From 1953 through 2007, approximately 139,400 acre-feet (acre-ft) of groundwater was pumped by the MCAGCC from the Surprise Spring subbasin. A regional-scale numerical groundwater flow model was developed using MODFLOW-2000 for the Surprise Spring, Deadman, Mesquite, and Mainside subbasins. The aquifer system was simulated by using three model layers representing the upper, middle, and lower aquifers. Measured groundwater levels
Proper interpretation of water quality requires consideration of the effects that contamination bias and sampling variability might have on measured analyte concentrations. The effect of contamination bias and sampling variability on major ion and total dissolved solids data in water samples collected in 48 of the 52 National Water-Quality Assessment Program study units from 1992–2010 is discussed in this report. Contamination bias and sampling variability can occur as a result of sample collection, processing, shipping, and analysis. Contamination bias can adversely affect interpretation of measured concentrations in comparison to standards or criteria. Sampling variability can help determine the reproducibility of an individual measurement or whether two measurements are different. Field blank samples help determine the frequency and magnitude of contamination bias, and replicate samples help determine the sampling variability (error) of measured analyte concentrations. Quality control data were evaluated for calcium, magnesium, sodium, potassium, chloride, sulfate, fluoride, silica, and total dissolved solids. A 99-percent upper confidence limit is calculated from field blanks to assess the potential for contamination bias. For magnesium, potassium, chloride, sulfate, and fluoride, potential contamination in more than 95 percent of environmental samples is less than or equal to the common maximum reporting level. Contamination bias has little effect on measured concentrations greater than 4.74 mg/L (milligrams per liter) for calcium, 14.98 mg/L for silica, 4.9 mg/L for sodium, and 120 mg/L for total dissolved solids. Estimates of sampling variability are calculated for high and low ranges of concentration for major ions and total dissolved solids. Examples showing the calculation of confidence intervals and how to determine whether measured differences between two water samples are significant are presented.
Groundwater quality in the Tahoe-Martis, Central Sierra, and Southern Sierra study units was investigated as part of the Priority Basin Project of the California Groundwater Ambient Monitoring and Assessment (GAMA) Program. The three study units are located in the Sierra Nevada region of California in parts of Nevada, Placer, El Dorado, Madera, Tulare, and Kern Counties. The GAMA Priority Basin Project is being conducted by the California State Water Resources Control Board, in collaboration with the U.S. Geological Survey (USGS) and the Lawrence Livermore National Laboratory. The project was designed to provide statistically robust assessments of untreated groundwater quality within the primary aquifer systems used for drinking water. The primary aquifer systems (hereinafter, primary aquifers) for each study unit are defined by the depth of the screened or open intervals of the wells listed in the California Department of Public Health (CDPH) database of wells used for municipal and community drinking-water supply. The quality of groundwater in shallower or deeper water-bearing zones may differ from that in the primary aquifers; shallower groundwater may be more vulnerable to contamination from the surface. The assessments for the Tahoe-Martis, Central Sierra, and Southern Sierra study units were based on water-quality and ancillary data collected by the USGS from 132 wells in the three study units during 2006 and 2007 and water-quality data reported in the CDPH database. Two types of assessments were made: (1) status, assessment of the current quality of the groundwater resource, and (2) understanding, identification of the natural and human factors affecting groundwater quality. The assessments characterize untreated groundwater quality, not the quality of treated drinking water delivered to consumers by water purveyors. Relative-concentrations (sample concentrations divided by benchmark concentrations) were used for evaluating groundwater quality for those constituents that have Federal or California regulatory or non-regulatory benchmarks for drinking-water quality. A relative-concentration (RC) greater than (>) 1.0 indicates a concentration above a benchmark. RCs for organic constituents (volatile organic compounds and pesticides) and special-interest constituents were classified as "high" (RC > 1.0), "moderate" (1.0 ≥ RC > 0.1), or "low" (RC ≤ 0.1). For inorganic constituents (major ions, trace elements, nutrients, and radioactive constituents), the boundary between low and moderate RCs was set at 0.5. A new metric, aquifer-scale proportion, was used in the status assessment as the primary metric for evaluating regional-scale groundwater quality. High aquifer-scale proportion is defined as the percentage of the area of the primary aquifers with RC > 1.0 for a particular constituent or class of constituents; moderate and low aquifer-scale proportions are defined as the percentages of the area of the primary aquifer with moderate and low RCs, respectively. Percentages are based on an areal rather than a volumetric basis. Two statistical approaches—grid-based, which used one value per grid cell, and spatially weighted, which used multiple values per grid cell—were used to calculate aquifer-scale proportions for individual constituents and classes of constituents. The spatially weighted estimates of high aquifer-scale proportions were within the 90-percent (%) confidence intervals of the grid-based estimates in all cases. The status assessment showed that inorganic constituents had greater high and moderate aquifer-scale proportions than did organic constituents in all three study units. In the Tahoe-Martis study unit, RCs for inorganic constituents with health-based benchmarks (primarily arsenic) were high in 20% of the primary aquifer, moderate in 13%, and low in 67%. In the Central Sierra study unit, aquifer-scale proportions for inorganic constituents with health-based benchmarks (primarily arsenic, uranium, fluoride, and molybdenum) were 41% high, 36% moderate, and 23% low. In the Southern Sierra study unit, 32, 34, and 34% of the primary aquifer had high, moderate, and low RCs of inorganic constituents with health-based benchmarks (primarily arsenic, uranium, fluoride, boron, and nitrate). The high aquifer-scale proportions for inorganic constituents with non-health-based benchmarks were 14, 34, and 24% for the Tahoe-Martis, Central Sierra, and Southern Sierra study units, respectively, and the primary constituent was manganese for all three study units. Organic constituents with health-based benchmarks were not present at high RCs in the primary aquifers of the Central Sierra and Southern Sierra study units, and were present at high RCs in only 1% of the Tahoe-Martis study unit. Moderate aquifer-scale proportions for organic constituents were < 5% in all three study units. Of the 173 organic constituents analyzed, 22 were detected, and of those 22, 17 have health-based benchmarks. Organic constituents were detected in 20, 27, and 40% of the primary aquifers in the Tahoe-Martis, Central Sierra, and Southern Sierra study units, respectively. Four organic constituents had study-unit detection frequencies of > 10%: the trihalomethane chloroform in the Tahoe-Martis study unit; chloroform and the herbicide simazine in the Central Sierra study unit; and chloroform, simazine, the herbicide atrazine, and the solvent perchloroethene in the Southern Sierra study unit. The second component of this study, the understanding assessment, identified the natural and human factors that may have affected groundwater quality in the three study units by evaluating statistical correlations between water-quality constituents and potential explanatory factors. The potential explanatory factors evaluated were land use, septic tank density, climate, relative position in the regional flow system, aquifer lithology, geographic location, well depth and depth to the top of the screened or open interval in the well, groundwater age distribution, pH, and dissolved oxygen concentration. Results of the statistical evaluations were used to explain the occurrence and distribution of constituents in the study units. Aquifer lithology (granitic, metamorphic, sedimentary, or volcanic rocks), groundwater age distribution [modern (recharged since 1952), pre-modern (recharged before 1952), or mixed (containing both modern and pre-modern recharge)], geographic location, pH, and dissolved oxygen were the most significant factors explaining the occurrence patterns of most inorganic constituents. High and moderate RCs of arsenic were associated with pre-modern and mixed-age groundwater and two distinct sets of geochemical conditions: (1) oxic, high-pH conditions, particularly in volcanic rocks, and (2) low-oxygen to anoxic conditions and low- to neutral-pH conditions, particularly in granitic rocks. In granitic and metamorphic rocks, high and moderate RCs of uranium were associated with pre-modern and mixed-age groundwater, low-oxygen to anoxic conditions, and location within parts of the Central Sierra and Southern Sierra study units known to have rocks with anomalously high uranium content compared to other parts of the Sierra Nevada. High and moderate RCs of uranium in sedimentary rocks were associated with pre-modern-age groundwater, oxic and high-pH conditions, and location in the Tahoe Valley South subbasin within the Tahoe-Martis study unit. Land use within 500 meters of the well and groundwater age were the most significant factors explaining occurrence patterns of organic constituents. Herbicide detections were most strongly associated with modern- and mixed-age groundwater from wells with agricultural land use. Trihalomethane detections were most strongly associated with modern- and mixed-age groundwater from wells with > 10% urban land use and (or) septic tank density > 7 tanks per square kilometer. Solvent detections were not significantly related to groundwater age. Eighty-three percent of the wells with modern- or mixed-age groundwater, and 86% of wells with detections of herbicides and (or) THMs had depths to the top of the screened or open interval of < 170 feet. These observations suggest that modern groundwater has infiltrated to depths of approximately 170 feet below land surface. Land use and occurrence of herbicides and solvents were the most significant factors explaining the occurrence of nitrate. Wells with > 5% agricultural land use and detection of a herbicide or solvent had the highest nitrate concentrations. Comparison between observed and predicted detection frequencies of perchlorate suggests that the perchlorate detected at concentrations < 1 microgram per liter likely reflects the distribution of perchlorate under natural conditions, and that the perchlorate detected at higher concentrations may reflect redistribution of originally natural perchlorate salts by irrigation in the agricultural areas of the Southern Sierra study unit.