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At least 307 records · Page 17Linked to original sources
USGS1989

Geochemistry of the Cambrian-Ordovician aquifer system in the northern Midwest, United States: D in Regional aquifer-system analysis

Distributions of solutes in aquifers of Cambrian and Ordovician age were studied in Minnesota, Wisconsin, Iowa, Illinois, northwestern Indiana, and northern Missouri to determine the sources of solutes and the probable chemical mechanisms that control regional variations in water quality. This work is part of the Northern Midwest Regional Aquifer-System Analysis project, whose objective is to describe and model the regional hydrogeology of the Cambrian- Ordovician aquifer system in the study region. The data base used included more than 3,000 ground-water-quality analyses from all major aquifers, but especially from the St. Peter, Jordan, and Mount Simon Sandstones and their equivalents. Regional variations in the water chemistry of glacial drift and other sedimentary units that overlie the Cambrian-Ordovician aquifer system in recharge areas in Minnesota, Iowa, Wisconsin, and Illinois were also studied, but to a lesser degree. The most important chemical variation in the aquifer is the change in water type from calcium-sodium-sulfate-bicarbonate water to sodium-calcium-sulfate-bicarbonate and sodium-chloride waters along the longest regional flow path from northwestern Iowa to the Illinois basin. Sodium predominance downgradient from the recharge area is probably related to mechanisms of ion exchange and shalemembrane filtration near the Illinois and Forest City basins. The most striking aspect of the distribution of dissolved solids and carbon isotopic content of bicarbonate is the increase in concentration and isotopic enrichment from southwestern Wisconsin, southern Minnesota, and northwestern Illinois south toward Missouri. This trend is perpendicular to the present hydraulic gradient that trends from northwestern Iowa southeastward to the Illinois basin. The distribution of dissolved solids defines a "plume" of dilute water having a dissolved-solids concentration of about 500 milligrams per liter, compared with surrounding concentrations more than twice as large. Distribution of the isotopic content of oxygen (<518O) and hydrogen (5D) in water closely parallels that of dissolved solids and shows covariance similar to modern meteoric water. The isotopic contents are more depleted (lighter) toward the south, perpendicular to the direction of current hydraulic gradients. The degree of depletion, compared with the isotopic content of modern recharge water, indicates that the plume and a significant fraction of the ground water in Iowa, northern Missouri, and possibly central Illinois may have originated as recharge during Pleistocene time. Distributions of dissolved trace constituents in the aquifers probably are related to the proximity to mineralogic sources as well as chemical and hydraulic mechanisms. For example, concentrations of some constituents, such as cadmium and arsenic, are largest in the vicinity of the Dakota Formation in northwestern Iowa. Other constituents, such as beryllium and vanadium, have larger concentrations near the edge of the Forest City basin in southwestern Iowa and northwestern Missouri. Strontium and fluoride concentrations generally increase from north to south, which suggests the input of these trace constituents during the recharge events. However, concentrations of bromide, radium-226, and lithium show distribution patterns similar to the "plume" defined by dissolved solids and isotopes of water, suggesting dilution of concentrations of trace constituents by Pleistocene recharge. Concentrations of other constituents are partly controlled by aquifer temperature, such as silica in south-central Iowa, and solubility controls, such as barium in northeastern Illinois. Additional information on the chemical and mineralogical composition of the aquifer matrix and the isotopically lightest ground water is needed to evaluate the hypothesis of Pleistocene mixing before more quantitative studies can be done to evaluate the different proposed mechanisms that have controlled and modified the water chemistry over time. This study, however, indicates that the ground water in the region is thousands of years old. The study also indicates that the major chemical trends in the aquifers probably are related as much to paleohydrogeologic flow systems during Pleistocene time as to the present flow system, which may postdate the retreat of the last ice sheet about 12,000 years ago.

Iowa, Indiana, Illinois, Michigan, Minnesota, Miss↗
USGS1996

Summary of the Snake River plain Regional Aquifer-System Analysis in Idaho and eastern Oregon

Regional aquifers underlying the 15,600-square-mile Snake River Plain in southern Idaho and eastern Oregon was studied as part of the U.S. Geological Survey's Regional Aquifer-System Analysis program. The largest and most productive aquifers in the Snake River Plain are composed of Quaternary basalt of the Snake River Group, which underlies most of the 10,8000-square-mile eastern plain. Aquifer tests and simulation indicate that transmissivity of the upper 200 feet of the basalt aquifer in the eastern plain commonly ranges from about 100,000 to 1,000,000 feet squared per day. However, transmissivity of the total aquifer thickness may be as much as 10 million feet squared per day. Specific yield of the upper 200 feet of the aquifer ranges from about 0.01 to 0.20. Average horizontal hydraulic conductivity of the upper 200 feet of the basalt aquifer ranges from less than 100 to 9,000 feet per day. Values may be one to several orders of magnitude higher in parts in individual flows, such as flow tops. Vertical hydraulic conductivity is probably several orders of magnitude lower than horizontal hydraulic conductivity and is generally related to the number of joints. Pillow lava in ancestral Snake River channels has the highest hydraulic conductivity of all rock types. Hydraulic conductivity of the basalt decreases with depth because of secondary filling of voids with calcite and silica. An estimated 80 to 120 million acre-feet of water is believed to be stored in the upper 200 feet of the basalt aquifer in the eastern plain. The most productive aquifers in the 4,800-square-mile western plain are alluvial sand and gravel in the Boise River valley. Although aquifer tests indicate that transmissivity of alluvium in the Boise River valley ranges from 5,000 to 160,000 feet squared per day, simulation suggests that average transmissivity of the upper 500 feet is generally less than 20,000 feet squared per day. Vertically averaged horizontal hydraulic conductivity of the upper 500 feet of alluvium ranges from about 4 to 40 feet per day; higher values can be expected in individual sand and gravel zones. Vertical hydraulic conductivity is considerably lower because of the presence of clay layers. Hydraulic heads measured in piezometers, interpreted from diagrams showing ground-water flow and equipotential lines and estimated by computer simulation, demonstrate that water movement is three dimensional through the rock framework. Natural recharge takes place along the margins of the plain where head decreases with depth; discharge takes place near some reaches of the Snake River and the Boise River where head increases with depth. Geothermal water in rhyolitic rocks in the western plain and western part of the eastern plain has higher hydraulic head than the overlying cold water. Geothermal water, therefore, moves upward and merges into the cold-water system. Basin water-budget analyses indicate that the volume of cold water. Carbon-14 age determinations, which indicate that residence time of geothermal water is 17,700 to 20,300 years, plus or minus 4,000 years, imply slow movement of water through the geothermal system. Along much of its length, the Snake River gains large quantities of ground water. On the eastern plain, the river gained about 1.9 million acre-feet of water between Blackfoot and Neeley, Idaho, in 1980. Between Milner and King Hill, Idaho, the river gained 4.7 million acre-feet, mostly as spring flow from the north side. Upstream from Blackfoot and in the vicinity of Lake Walcott, the rover loses flow to ground water during parts or all of the year. On the western plain, river gains from ground water are small relative to those on the eastern plain; most are from seepage. Streams in tributary drainage basins supply calcium/bicarbonate type and calcium/magnesium/bicarbonate type water to the plain. Water type is a reflection of the chemical composition of rocks in the drainage basin, Concentrations of dissolved solids are smallest, about 50 milligrams per liter, in streams such as the Boise River that drain areas of granitic rocks; concentrations are greatest, about 400 milligrams per liter, in streams such as the Owyhee and Raft Rivers that drain area of sedimentary rocks. Water chemistry reflects the interaction of surface water and ground water. The chemical composition of ground water in the plain is essentially the same as that in streamflow and groundwater discharge from tributary drainage basins. Tributary drainage basins supplied 85 percent of the ground-water recharge in the eastern plain during 1980 and a nearly equivalent percentage of the solute load in ground water; human activities and dissolution of minerals supplied the other solutes. Dissolved-solids concentrations in ground water were generally less than 400 milligrams per liter. Water from the lower geothermal system is chemically different from water from the upper cold-water system. Geothermal water typically has greater concentrations of sodium, bicarbonate, sulfate, chloride, fluoride, silica, arsenic, boron, and lithium and smaller concentrations of calcium, magnesium, and hydrogen. Difference are attributed to ion exchange as geothermal moves through the rock framework. Irrigation, mostly on the Snake River Plain, accounted for about 96 percent of consumptive water use in Idaho during 1980. The use of surface water for irrigation for more than 100 years has caused major changes in the hydrologic system on the plain. Construction of dams, reservoirs, and diversifications effected planned changes in the surface-water system but resulted in largely unplanned changes in the ground-water system. During those years of irrigation, annual recharge in the main part of the eastern plain increased to about 6.7 million acre-feet in 1980, or by about 70 percent. Most of the increase was from percolation of surface water diverted for irrigation. From preirrigation to 1952, groundwater storage increased about 24 million acre-feet, and storage decreased from 1952 to 1964 and from 1976 to 1980 because of below-normal precipitation and increased withdrawals of ground water for irrigation. Annual ground-water discharge increased to about 7.1 million acre-feet in 1980, or about 80 percent since the start of irrigation. About 10 percent of the 1980 total discharge was ground-water pumpage. About 3.1 million acres, or almost one-third of the plain, was irrigated during 1980: 2.0 million acres with surface water, 1.0 million acres with ground water, and 0.1 million acres with combined surface and ground water. About 8.9 million acre-feet of Snake River water was diverted for irrigation during 1980 and 2.3 million acre-feet of ground water was pumped from 5,300 wells. Most irrigation wells on the eastern plain are open to basalt. About two-thirds of them yield more than 1,500 gallons per minute with a reported maximum of 7,240 gallons per minute; drawdown is less than 20 feet in two-thirds of the wells. Most irrigation wells on the western plain are open to sedimentary rocks. About one-third of them yield more than 1,00 gallons per minute with a reported maximum of 3,850 gallons per minute; drawndown is less than 20 feet in about one-fifth of the wells. The major instream use of water on the Snake River Plain is hydroelectric power generation. Fifty-two million acre-feet of water generated 2.6 million megawatthours of electricity during 1980. Digital computer ground-water flows models of the eastern and western plain reasonably simulated regional changes in water levels and ground-water discharges from 1880 (preirrigation) to 1980. Model results support the concept of three-dimensional flow and the hypotheses of no underflow between the eastern and western plain. Simulation of the regional aquifer system in the eastern plain indicates that is 1980 hydrologic conditions, including pumpage, were to remain the same for another 30 years, moderate declines in ground-water levels and decreases in spring discharges would continue. Increased ground-water pumpage to irrigate an additional 1 million acres could cause ground-water levels to decline a few tens of feet in the central part of the plain and could cause corresponding decreases in ground-water discharge. A combination of actions such as increased ground-water pumpage and decreased use of surface water for irrigation (resulting in reduced recharge) would accentuate the changes.

Idaho;Oregon↗
USGS2017

Germanium and indium

Germanium and indium are two important elements used in electronics devices, flat-panel display screens, light-emitting diodes, night vision devices, optical fiber, optical lens systems, and solar power arrays. Germanium and indium are treated together in this chapter because they have similar technological uses and because both are recovered as byproducts, mainly from copper and zinc sulfides. The world’s total production of germanium in 2011 was estimated to be 118 metric tons. This total comprised germanium recovered from zinc concentrates, from fly ash residues from coal burning, and from recycled material. Worldwide, primary germanium was recovered in Canada from zinc concentrates shipped from the United States; in China from zinc residues and coal from multiple sources in China and elsewhere; in Finland from zinc concentrates from the Democratic Republic of the Congo; and in Russia from coal. World production of indium metal was estimated to be about 723 metric tons in 2011; more than one-half of the total was produced in China. Other leading producers included Belgium, Canada, Japan, and the Republic of Korea. These five countries accounted for nearly 95 percent of primary indium production. Deposit types that contain significant amounts of germanium include volcanogenic massive sulfide (VMS) deposits, sedimentary exhalative (SEDEX) deposits, Mississippi Valley-type (MVT) lead-zinc deposits (including Irish-type zinc-lead deposits), Kipushi-type zinc-lead-copper replacement bodies in carbonate rocks, and coal deposits. More than one-half of the byproduct indium in the world is produced in southern China from VMS and SEDEX deposits, and much of the remainder is produced from zinc concentrates from MVT deposits. The Laochang deposit in Yunnan Province, China, and the VMS deposits of the Murchison greenstone belt in Limpopo Province, South Africa, provide excellent examples of indium-enriched deposits. The SEDEX deposits at Bainiuchang, China (located in southeastern Yunnan Province), and the Dabaoshan SEDEX deposit (located in the Nanling region of China) contain indium-enriched sphalerite. Another major potential source of indium occurs in the polymetallic tin-tungsten belt in the Eastern Cordillera of the Andes Mountains of Bolivia. Deposits there occur as dense arrays of narrow, elongate, indium-enriched tin oxide-polymetallic sulfide veins in volcanic rocks and porphyry stocks. Information about the behavior of germanium and indium in the environment is limited. In surface weathering environments, germanium and indium may dissolve from host minerals and form complexes with chloride, fluoride, hydroxide, organic matter, phosphate, or sulfate compounds. The tendency for germanium and indium to be dissolved and transported largely depends upon the pH and temperature of the weathering solutions. Because both elements are commonly concentrated in sulfide minerals, they can be expected to be relatively mobile in acid mine drainage where oxidative dissolution of sulfide minerals releases metals and sulfuric acid, resulting in acidic pH values that allow higher concentrations of metals to be dissolved into solution.

Professional Paper↗
USGS1979

Summary appraisals of the nation's ground-water resources– South Atlantic-Gulf region

Precipitation in the 270,000-square-mile South Atlantic-Gulf Region ranges from 44 to 80 inches, and the average runoff is about 15 inches. The ground-water discharge that forms the base flow of streams is conservatively estimated to be about 78,000 million gallons per day the equivalent of about 6 inches of precipitation. On this basis, the regional sustained ground-water supply is about 286,000 gallons per day per square mile. Projected water use through 2020 indicates that about 10 percent of the supply will meet the region's requirement for ground water. Enormous quantities of ground water are available in the South Atlantic-Gulf States in the extensive aquifers that underlie the Coastal Plain province. Large supplies of ground water can be developed also in places in the Cumberland Plateau and the Valley and Ridge provinces. In the Piedmont and Blue Ridge provinces ground water is available only in modest quantities. The principal Coastal Plain aquifers consist largely of deltaic sand and gravel deposits of Cretaceous to Quaternary age; however, a notable exception is the highly permeable Tertiary limestone aquifer, which underlies parts of four States. Ground water in the Blue Ridge and the Valley and Ridge provinces is available from openings along fissures and joints in consolidated rocks and from the unconsolidated sand and gravel in the residuum and alluvium that overlie the bedrock. In parts of these areas faulting and folding has created favorable conditions for the development of moderate supplies of ground water. In the Piedmont province modest quantities of water are available from joints and fractures. Solution cavities in massive limestone units in some areas underlying the Cumberland Plateau section yield very large quantities of ground water. Most of the major Coastal Plain aquifers are recharged where they are exposed and water moves downdip to the south. The general direction of ground-water movement in the Coastal Plain aquifers is seaward. There is, however, movement of water vertically and laterally that affects pressure and quality in every aquifer. Ground water of good chemical and physical quality is available generally except in a small area in western Alabama and eastern Mississippi and in some small coastal areas. Freshwater extends to depths of slightly more than 3,000 feet in some areas. In many areas, water can be produced that does not require any treatment for general use. The more common objectionable constituents or properties are excessive iron, fluoride, hardness, color, and acidity. Contamination or pollution of ground water is not a major regional problem, but it is significant in local areas. Many of these local problems of contamination were the result of earlier improper disposal of oil-field and industrial waste. Saltwater intrusion either directly from the sea or from estuaries has been reported in every State in the region, and the potential for the proliferation of this problem is very large. The relationship of ground water and surface water is significant at many places in the region where large ground-water withdrawals affect swamps, lakes, and the flow of streams and springs. There is a potential in some areas for using ground water during dry periods for low-flow augmentation of stream supplies. In other areas it is feasible to recharge ground-water reservoirs artificially by means of injection wells, pits, and water spreading. Although large water-level declines caused by withdrawals have occurred locally, water-level changes have been small or modest when considered on a regional basis owing to the abundant rainfall and favorable recharge conditions. The saline-water resources of the region are known to be extremely large. In some areas where the availability of freshwater is limited, saline ground water is available for desalinization to supplement freshwater supplies. Also, the saline aquifers are potential storage sites for injected freshwater. Ground-water problems generally are not severe. Critical situations are restricted to areas where large quantities of ground water are being withdrawn or where aquifers are contaminated by oil-field or industrial waste. Large withdrawals in coastal areas have caused some saltwater intrusion. In other localities, highly mineralized water may have migrated along fault zones to freshwater aquifers. Many of the present problems can be resolved or ameliorated by redistributing withdrawals or developing alternative water sources.

Alabama, Florida, Georgia, Mississippi, North Caro↗
USGS2005

Hydrologic characteristics of the Agua Fria National Monument, central Arizona, determined from the reconnaissance study

Hydrologic conditions in the newly created Agua Fria National Monument were characterized on the basis of existing hydrologic and geologic information, and streamflow data collected in May 2002. The study results are intended to support the Bureau of Land Management's future water-resource management responsibilities, including quantification of a Federal reserved water right within the monument. This report presents the study results, identifies data deficiencies, and describes specific approaches for consideration in future studies. Within the Agua Fria National Monument, the Agua Fria River flows generally from north to south, traversing almost the entire 23-mile length of the monument. Streamflow has been measured continuously at a site near the northern boundary of the monument since 1940. Streamflow statistics for this site, and streamflow measurements from other sites along the Agua Fria River, indicate that the river is perennial in the northern part of the monument but generally is intermittent in downstream reaches. The principal controls on streamflow along the river within the monument appear to be geology, the occurrence and distribution of alluvium, inflow at the northern boundary and from tributary canyons, precipitation, and evapotranspiration. At present, (2004) there is no consistent surface-water quality monitoring program being implemented for the monument. Ground-water recharge within the monument likely results from surface-water losses and direct infiltration of precipitation. Wells are most numerous in the Cordes Junction and Black Canyon City areas. Only eight wells are within the monument. Ground-water quality data for wells in the monument area consist of specific-conductance values and fluoride concentrations. During the study, ground-water quality data were available for only one well within the monument. No ground-water monitoring program is currently in place for the monument or surrounding areas.

Scientific Investigations Report↗
USGS2004

Water resources of Sweetwater County, Wyoming

Sweetwater County is located in the southwestern part of Wyoming and is the largest county in the State. A study to quantify the availability and describe the chemical quality of surface-water and ground-water resources in Sweetwater County was conducted by the U.S. Geological Survey in cooperation with the Wyoming State Engineer’s Office. Most of the county has an arid climate. For this reason a large amount of the flow in perennial streams within the county is derived from outside the county. Likewise, much of the ground-water recharge to aquifers within the county is from flows into the county, and occurs slowly. Surface-water data were not collected as part of the study. Evaluations of streamflow and stream-water quality were limited to analyses of historical data and descriptions of previous investigations. Forty-six new ground-water-quality samples were collected as part of the study and the results from an additional 782 historical ground-water-quality samples were reviewed. Available hydrogeologic characteristics for various aquifers throughout the county also are described. Flow characteristics of streams in Sweetwater County vary substantially depending on regional and local basin characteristics and anthropogenic factors. Because precipitation amounts in the county are small, most streams in the county are ephemeral, flowing only as a result of regional or local rainfall or snowmelt runoff. Flows in perennial streams in the county generally are a result of snowmelt runoff in the mountainous headwater areas to the north, west, and south of the county. Flow characteristics of most perennial streams are altered substantially by diversions and regulation. Water-quality characteristics of selected streams in and near Sweetwater County during water years 1974 through 1983 were variable. Concentrations of dissolved constituents, suspended sediment, and bacteria generally were smallest at sites on the Green River because of resistant geologic units, increased vegetative cover, large diluting streamflows, and large reservoirs. Concentrations of dissolved constituents, suspended sediment, and bacteria generally were largest at sites in the Big Sandy River and Bitter Creek Basins. Some nutrient concentrations and bacteria counts exceeded various State and Federal water-quality criteria. Historical and recent anthropogenic activities contributed to natural sources of many dissolved constituents and suspended sediment. Both water-table and artesian conditions occur in aquifers within the county. Shallow ground water is available throughout the county, although much of it is only marginally suitable or is unsuitable for domestic and irrigation uses mainly because of high total dissolved solids (TDS) concentrations. Suitable ground water for livestock use can be found in most areas of the county. Ground-water quality tends to deteriorate with increasing distance from recharge areas and with increasing depth below land surface. Ground water from depths of greater than a few thousand feet tends to have TDS concentrations that make it moderately saline to briny. In some areas even shallow ground water has moderately saline TDS concentrations. Specific constituents in parts of some aquifers in the county occur in relatively high concentrations when compared to U.S. Environmental Protection Agency drinking-water standards. Relatively high concentrations of sulfate, fluoride, boron, iron, and manganese were found in several aquifers. Many ground-water samples from the Battle Spring aquifer in the Great Divide Structural Basin had high radionuclide concentrations. The estimated mean daily water use in Sweetwater County in 2000 was 170.73 million gallons per day. Irrigation was the largest single use of water in the county with an estimated mean use of more than 92 million gallons per day. Surface water irrigation accounted for nearly 90 percent of the total irrigation water used in 2000. Although ground water is used to a much lesser extent than surface water, in many areas of the county it is the only source of water available.

Wyoming↗
USGS2004

Water-quality characteristics of quaternary unconsolidated-deposit aquifers and lower tertiary aquifers of the Bighorn Basin, Wyoming and Montana, 1999-2001

As part of the Yellowstone River Basin National Water Quality Assessment study, ground-water samples were collected from Quaternary unconsolidated-deposit and lower Tertiary aquifers in the Bighorn Basin of Wyoming and Montana from 1999 to 2001. Samples from 54 wells were analyzed for physical characteristics, major ions, trace elements, nutrients, dissolved organic carbon, radionuclides, pesticide compounds, and volatile organic compounds (VOCs) to evaluate current water-quality conditions in both aquifers. Water-quality samples indicated that waters generally were suitable for most uses, and that natural conditions, rather than the effects of human activities, were more likely to limit uses of the waters. Waters in both types of aquifers generally were highly mineralized, and total dissolved-solids concentrations frequently exceeded the U.S. Environmental Protection Agency (USEPA) Secondary Maximum Contaminant Level (SMCL) of 500 milligrams per liter (mg/L). Because of generally high mineralization, waters from nearly one-half of the samples from Quaternary aquifers and more than one-half of the samples from lower Tertiary aquifers were not classified as fresh (dissolved-solids concentration were not less than 1,000 mg/L). The anions sulfate, fluoride, and chloride were measured in some ground-water samples at concentrations greater than SMCLs. Most waters from the Quaternary aquifers were classified as very hard (hardness greater than 180 mg/L), but hardness varied much more in waters from the lower Tertiary aquifers and ranged from soft (less than 60 mg/L) to very hard (greater than 180 mg/L). Major-ion chemistry varied with dissolved-solids concentrations. In both types of aquifers, the predominant anion changes from bicarbonate to sulfate with increasing dissolved-solids concentrations. Samples from Quaternary aquifers with fresh waters generally were calcium-bicarbonate, calcium-sodium-bicarbonate, and calcium-sodium-sulfate-bicarbonate type waters, whereas samples with larger concentrations generally were calcium-sodium-sulfate, calcium-sulfate, or sodium-sulfate-type waters. In the lower Tertiary aquifers, samples with fresh waters generally were sodium-bicarbonate or sodium-bicarbonate-sulfate type waters, whereas samples with larger concentrations were sodium-sulfate or calcium-sodium-sulfate types. Concentrations of most trace elements in both types of aquifers generally were small and most were less than applicable USEPA standards. The trace elements that most often did not meet USEPA secondary drinking-water standards were iron and manganese. In fact, the SMCL for manganese was the most frequently exceeded standard; 68 percent of the samples from the Quaternary aquifers and 31 percent of the samples from the lower Tertiary aquifers exceeded the manganese standard. Geochemical conditions may control manganese in both aquifers as concentrations in Quaternary aquifers were negatively correlated with dissolved oxygen concentrations and concentrations in lower Tertiary aquifers decreased with increasing pH. Elevated nitrate concentrations, in addition to detection of pesticides and VOCs in both aquifers, indicated some effects of human activities on ground-water quality. Nitrate concentrations in 36 percent of the wells in Quaternary aquifers and 28 percent of the wells in lower Tertiary aquifers were greater than 1 mg/L, which may indicate ground-water contamination from human sources. The USEPA drinking-water Maximum Contaminant Level (MCL) for nitrate, 10 mg/L, was exceeded in 8 percent of samples collected from Quaternary aquifers and 3 percent from lower Tertiary aquifers. Nitrate concentrations in Quaternary aquifers were positively correlated with the percentage of cropland and other agricultural land (non-cropland), and negatively correlated with rangeland and riparian land. In the lower Tertiary aquifers, nitrate concentrations only were correlated with the percentage of cropland. Concentratio

Scientific Investigations Report↗
USGS2005

Evaluation of geohydrologic framework, recharge estimates and ground-water flow of the Joshua Tree area, San Bernardino County, California

Ground water historically has been the sole source of water supply for the community of Joshua Tree in the Joshua Tree ground-water subbasin of the Morongo ground-water basin in the southern Mojave Desert. The Joshua Basin Water District (JBWD) supplies water to the community from the underlying Joshua Tree ground-water subbasin. The JBWD is concerned with the long-term sustainability of the underlying aquifer. To help meet future demands, the JBWD plans to construct production wells in the adjacent Copper Mountain ground-water subbasin. As growth continues in the desert, there may be a need to import water to supplement the available ground-water resources. In order to manage the ground-water resources and to identify future mitigating measures, a thorough understanding of the ground-water system is needed. The purpose of this study was threefold: (1) improve the understanding of the geohydrologic framework of the Joshua Tree and Copper Mountain ground-water subbasins, (2) determine the distribution and quantity of recharge using field and numerical techniques, and (3) develop a ground-water flow model that can be used to help manage the water resources of the region. The geohydrologic framework was refined by collecting and interpreting water-level and water-quality data, geologic and electric logs, and gravity data. The water-bearing deposits in the Joshua Tree and Copper Mountain ground-water subbasins are Quarternary alluvial deposits and Tertiary sedimentary and volcanic deposits. The Quarternary alluvial deposits were divided into two aquifers (referred to as the 'upper' and the 'middle' alluvial aquifers), which are about 600 feet (ft) thick, and the Tertiary sedimentary and volcanic deposits were assigned to a single aquifer (referred to as the 'lower' aquifer), which is as thick as 1,500 ft. The ground-water quality of the Joshua Tree and Copper Mountain ground-water subbasins was defined by collecting 53 ground-water samples from 15 wells (10 in the Joshua Tree ground-water subbasin and 5 in the Copper Mountain ground-water subbasin) between 1980 and 2002 and analyzing the samples for major ions, nutrients, and selected trace elements. Selected samples also were analyzed for oxygen-18, deuterium, tritium, and carbon-14. The water-quality data indicated that dissolved solids and nitrate concentrations were below regulatory limits for potable water; however, fluoride concentrations in the lower aquifer exceeded regulatory limits. Arsenic concentrations and chromium concentrations were generally below regulatory limits; however, arsenic concentrations measured in water from wells perforated in the lower aquifer exceeded regulatory limits. The carbon-14 activities ranged from 2 to 72 percent modern carbon and are consistent with uncorrected ground-water ages (time since recharge) of about 32,300 to 2,700 years before present. The oxygen-18 and deuterium composition of water sampled from the upper aquifer is similar to the volume-weighted composition of present-day winter precipitation indicating that winter precipitation was the predominant source of ground-water recharge. Field studies, conducted during water years 2001 through 2003 to determine the distribution and quantity of recharge, included installation of instrumented boreholes in selected washes and at a nearby control site. Core material and cuttings from the boreholes were analyzed for physical, chemical, and hydraulic properties. Instruments installed in the boreholes were monitored to measure changes in matric potential and temperature. Borehole data were supplemented with temperature data collected from access tubes installed at additional sites along study washes. Streambed hydraulic properties and the response of instruments to infiltration were measured using infiltrometers. Physical and geochemical data collected away from the stream channels show that direct infiltration of precipitation to depths below the root zone and subsequent gro

Scientific Investigations Report↗
USGS2004

Effects of surface applications of biosolids on soil, crops, ground water, and streambed sediment near Deer Trail, Colorado, 1999-2003

The U.S. Geological Survey, in cooperation with Metro Wastewater Reclamation District and North Kiowa Bijou Groundwater Management District, studied natural geochemical effects and the effects of biosolids applications to the Metro Wastewater Reclamation District properties near Deer Trail, Colorado, during 1999 through 2003 because of public concern about potential contamination of soil, crops, ground water, and surface water from biosolids applications. Parameters analyzed for each monitoring component included arsenic, cadmium, copper, lead, mercury, molybdenum, nickel, selenium, and zinc (the nine trace elements regulated by Colorado for biosolids), gross alpha and gross beta radioactivity, and plutonium, as well as other parameters. Concentrations of the nine regulated trace elements in biosolids were relatively uniform and did not exceed applicable regulatory standards. All plutonium concentrations in biosolids were below the minimum detectable level and were near zero. The most soluble elements in biosolids were arsenic, molybdenum, nickel, phosphorus, and selenium. Elevated concentrations of bismuth, mercury, phosphorus, and silver would be the most likely inorganic biosolids signature to indicate that soil or streambed sediment has been affected by biosolids. Molybdenum and tungsten, and to a lesser degree antimony, cadmium, cobalt, copper, mercury, nickel, phosphorus, and selenium, would be the most likely inorganic 'biosolids signature' to indicate ground water or surface water has been affected by biosolids. Soil data indicate that biosolids have had no measurable effect on the concentration of the constituents monitored. Arsenic concentrations in soil of both Arapahoe and Elbert County monitoring sites (like soil from all parts of Colorado) exceed the Colorado soil remediation objectives and soil cleanup standards, which were determined by back-calculating a soil concentration equivalent to a one-in-a-million cumulative cancer risk. Lead concentrations in soil slightly exceed the U.S. Environmental Protection Agency toxicity-derived ecological soil-screening levels for avian wildlife. Plutonium concentration in the soil was near zero. Wheat-grain data were insufficient to determine any measurable effects from biosolids. Comparison with similar data from other parts of North America where biosolids were not applied indicates similar concentrations. However, the Deer Trail study area had higher nickel concentrations in wheat from both the biosolids-applied fields and the control fields. Plutonium content of the wheat was near zero. Ground-water levels generally declined at most wells during 1999 through 2003. Ground-water quality did not correlate with ground-water levels. Vertical ground-water gradients during 1999 through 2003 indicate that bedrock ground-water resources downgradient from the biosolids-applied areas are not likely to be contaminated by biosolids applications unless the gradients change as a result of pumping. Ground-water quality throughout the study area varied over time at each site and from site to site at the same time, but plutonium concentrations in the ground water always were near zero. Inorganic concentrations at well D6 were relatively high compared to other ground-water sites studied. Ground-water pH and concentrations of fluoride, nitrite, aluminum, arsenic, barium, chromium, cobalt, copper, lead, mercury, nickel, silver, zinc, and plutonium in the ground water of the study area met Colorado standards. Concentrations of chloride, sulfate, nitrate, boron, iron, manganese, and selenium exceeded Colorado ground-water standards at one or more wells. Nitrate concentrations at well D6 significantly (alpha = 0.05) exceeded the Colorado regulatory standard. Concentrations of arsenic, cadmium, chromium, lead, mercury, nickel, and zinc in ground water had no significant (alpha = 0.05) upward trends. During 1999-2003, concentrations of nitrate, copper, molybdenum, and selenium

Scientific Investigations Report↗
USGS2005

Assessment of water quality, benthic invertebrates, and periphyton in the Threemile Creek basin, Mobile, Alabama, 1999-2003

The U.S. Geological Survey conducted a 4-year investigation of water quality and aquatic-community structure in Threemile Creek, an urban stream that drains residential areas in Mobile, Alabama. Water-quality samples were collected between March 2000 and September 2003 at four sites on Threemile Creek, and between March 2000 and October 2001 at two tributary sites that drain heavily urbanized areas in the watershed. Stream samples were analyzed for major ions, nutrients, fecal-indicator bacteria, and selected organic wastewater compounds. Continuous measurements of dissolved-oxygen concentrations, water temperature, specific conductance, and turbidity were recorded at three sites on Threemile Creek during 1999?2003. Aquatic-community structure was evaluated by conducting one survey of the benthic invertebrate community and multiple surveys of the algal community (periphyton). Benthic invertebrate samples were collected in July 2000 at four sites on Threemile Creek; periphyton samples were collected at four sites on Threemile Creek and the two tributary sites during 2000 ?2003. The occurrence and distribution of chemical constituents in the water column provided an initial assessment of water quality in the streams; the structure of the benthic invertebrate and algal communities provided an indication of the cumulative effects of water quality on the aquatic biota. Information contained in this report can be used by planners and resource managers in the evaluation of proposed total maximum daily loads and other restoration efforts that may be implemented on Threemile Creek. The three most upstream sites on Threemile Creek had similar water chemistry, characterized by a strong calcium-bicarbonate component; the most downstream site on Threemile Creek was affected by tidal fluctuations and mixing from Mobile Bay and had a strong sodium-chloride component. The water chemistry at the tributary site on Center Street was characterized by a strong sodium-chloride component; the water chemistry at the second tributary site, Toulmins Spring Branch, was characterized by a strong calcium component without a dominant anionic species. The ratios of sodium to chloride at the tributary at Center Street were higher than typical values for seawater, indicating that sources other than seawater (such as leaking or overflowing sewer systems or industrial discharge) likely are contributors to the increased levels of sodium and chloride. Concentrations of fluoride and boron also were elevated at this site, indicating possible anthropogenic sources. Dissolved-oxygen concentrations were not always within levels established by the Alabama Department of Environmental Management; continuous monitors recorded dissolved-oxygen concentrations that were repeatedly less than the minimum criterion (3.0 milligrams per liter) at the most downstream site on Threemile Creek. Water temperature exceeded the recommended criterion (32.2 degrees Celsius) at five of six sites in the Threemile Creek basin. The pH values were within established criteria (6.0 ? 8.5) at sites on Threemile Creek; however, pH values ranged from 7.2 to 10.0 at the tributary at Center Street and from 6.6 to 9.9 at Toulmins Spring Branch. Nutrient concentrations in the Threemile Creek basin reflect the influences of both land use and the complex hydrologic systems in the lower part of the basin. Nitrite-plus-nitrate concentrations exceeded U.S. Environmental Protection Agency ecoregion nutrient criteria in 88 percent of the samples. In 45 percent of the samples, total phosphorus concentrations exceeded the U.S. Environmental Protection Agency goal of 0.1 milligram per liter for preventing nuisance aquatic growth. Ratios of nitrogen to phosphorus indicate that both nutrients have limiting effects. Median concentrations of enterococci and fecal coliform bacteria were highest at the two tributary sites and lowest at the most upstream site on Threemile Creek. In general, concentrations o

Scientific Investigations Report↗
USGS2005

Arsenic in ground water in selected parts of southwestern Ohio, 2002-03

Arsenic concentrations were measured in 57 domestic wells in Preble, Miami, and Shelby Counties, in southwestern Ohio. The median arsenic concentration was 7.1 ?g/L (micrograms per liter), and the maximum was 67.6 ?g/L. Thirty-seven percent of samples had arsenic concentrations greater than the U.S. Environmental Protection Agency drinking-water standard of 10 ?g/L. Elevated arsenic concentrations (>10 ?g/L) were detected over the entire range of depths sampled (42 to 221 feet) and in each of three aquifer types, Silurian carbonate bedrock, glacial buried-valley deposits, and glacial till with interbedded sand and gravel. One factor common in all samples with elevated arsenic concentrations was that iron concentrations were greater than 1,000 ?g/L. The observed correlations of arsenic with iron and alkalinity are consistent with the hypothesis that arsenic was released from iron oxides under reducing conditions (by reductive dissolution or reductive desorption). Comparisons among the three aquifer types revealed some differences in arsenic occurrence. For buried-valley deposits, the median arsenic concentration was 4.6 ?g/L, and the maximum was 67.6 ?g/L. There was no correlation between arsenic concentrations and depth; the highest concentrations were at intermediate depths (about 100 feet). Half of the buried-valley samples were estimated to be methanic. Most of the samples with elevated arsenic concentrations also had elevated concentrations of dissolved organic carbon and ammonia. For carbonate bedrock, the median arsenic concentration was 8.0 ?g/L, and the maximum was 30.7 ?g/L. Arsenic concentrations increased with depth. Elevated arsenic concentrations were detected in iron- or sulfate-reducing samples. Arsenic was significantly correled with molybdenum, strontium, fluoride, and silica, which are components of naturally ocurring minerals. For glacial till with interbedded sand and gravel, half of the samples had elevated arsenic concentrations. The median was 11.4 ?g/L, and the maximum was 27.6 ?g/L. At shallow depths (<100 feet), this aquifer type had higher arsenic and iron concentrations than carbonate bedrock. It is not known whether these observed differences among aquifer types are related to variations in (1) arsenic content of the aquifer material, (2) organic carbon content of the aquifer material, (3) mechanisms of arsenic mobilization (or uptake), or (4) rates of arsenic mobilization (or uptake). A followup study that includes solid-phase analyses and geochemical modeling was begun in 2004 in northwestern Preble County.

Scientific Investigations Report↗
USGS2005

Ground-water quality in the carbonate-rock aquifer of the Great Basin, Nevada and Utah, 2003

The carbonate-rock aquifer of the Great Basin is named for the thick sequence of Paleozoic limestone and dolomite with lesser amounts of shale, sandstone, and quartzite. It lies primarily in the eastern half of the Great Basin and includes areas of eastern Nevada and western Utah as well as the Death Valley area of California and small parts of Arizona and Idaho. The carbonate-rock aquifer is contained within the Basin and Range Principal Aquifer, one of 16 principal aquifers selected for study by the U.S. Geological Survey’s National Water- Quality Assessment Program. Water samples from 30 ground-water sites (20 in Nevada and 10 in Utah) were collected in the summer of 2003 and analyzed for major anions and cations, nutrients, trace elements, dissolved organic carbon, volatile organic compounds (VOCs), pesticides, radon, and microbiology. Water samples from selected sites also were analyzed for the isotopes oxygen-18, deuterium, and tritium to determine recharge sources and the occurrence of water recharged since the early 1950s. Primary drinking-water standards were exceeded for several inorganic constituents in 30 water samples from the carbonate-rock aquifer. The maximum contaminant level was exceeded for concentrations of dissolved antimony (6 μg/L) in one sample, arsenic (10 μg/L) in eleven samples, and thallium (2 μg/L) in one sample. Secondary drinking-water regulations were exceeded for several inorganic constituents in water samples: chloride (250 mg/L) in five samples, fluoride (2 mg/L) in two samples, iron (0.3 mg/L) in four samples, manganese (0.05 mg/L) in one sample, sulfate (250 mg/L) in three samples, and total dissolved solids (500 mg/L) in seven samples. Six different pesticides or metabolites were detected at very low concentrations in the 30 water samples. The lack of VOC detections in water sampled from most of the sites is evidence thatVOCs are not common in the carbonate-rock aquifer. Arsenic values for water range from 0.7 to 45.7 μg/L, with a median value of 9.6 μg/L. Factors affecting arsenic concentration in the carbonate-rock aquifer in addition to geothermal heating are its natural occurrence in the aquifer material and time of travel along the flow path. Most of the chemical analyses, especially for VOCs and nutrients, indicate little, if any, effect of overlying land-use patterns on ground-water quality. The water quality in recharge areas for the aquifer where human activities are more intense may be affected by urban and/or agricultural land uses as evidenced by pesticide detections. The proximity of the carbonate-rock aquifer at these sites to the land surface and the potential for local recharge to occur through the fractured rock likely results in the occurrence of these and other land-surface related contaminants in the ground water. Water from sites sampled near outcrops of carbonate-rock aquifer likely has a much shorter residence time resulting in a potential for detection of anthropogenic or land-surface related compounds. Sites located in discharge areas of the flow systems or wells that are completed at a great depth below the land surface generally show no effects of land-use activities on water quality. Flow times within the carbonate-rock aquifer, away from recharge areas, are on the order of thousands of years, so any contaminants introduced at the land surface that will not degrade along the flow path have not reached the sampled sites in these areas.

Nevada, Utah↗
USGS2006

Water resources of Carbon County, Wyoming

Carbon County is located in the south-central part of Wyoming and is the third largest county in the State. A study to describe the physical and chemical characteristics of surface-water and ground-water resources in Carbon County was conducted by the U.S. Geological Survey in cooperation with the Wyoming State Engineer's Office. Evaluations of streamflow and stream-water quality were limited to analyses of historical data and descriptions of previous investigations. Surface-water data were not collected as part of the study. Forty-five ground-water-quality samples were collected as part of the study and the results from an additional 618 historical ground-water-quality samples were reviewed. Available hydrogeologic characteristics for various aquifers in hydrogeologic units throughout the county also are described. Flow characteristics of streams in Carbon County vary substantially depending on regional and local basin char-acteristics and anthropogenic factors. Precipitation in the county is variable with high mountainous areas receiving several times the annual precipitation of basin lowland areas. For this reason, streams with headwaters in mountainous areas generally are perennial, whereas most streams in the county with headwaters in basin lowland areas are ephemeral, flowing only as a result of regional or local rainfall or snowmelt runoff. Flow characteristics of most perennial streams are altered substantially by diversions and regulation. Water-quality characteristics of selected streams in and near Carbon County during water years 1966 through 1986 varied. Concentrations of dissolved constituents and suspended sediment were smallest at sites on streams with headwaters in mountainous areas because of resistant geologic units, large diluting streamflows, and increased vegetative cover compared to sites on streams with headwaters in basin lowlands. Both water-table and artesian conditions occur in aquifers within the county. Shallow ground water is available throughout the county, although much of it is only marginally suitable or is unsuitable for domestic and irrigation uses mainly because of high total dissolved solids (TDS) concentrations. Suitable ground water for livestock use is available in most areas of the county. Ground-water quality tends to deteriorate with increasing distance from recharge areas and with increasing depth below land surface. Ground water from depths greater than a few thousand feet tends to have TDS concentrations that make it moderately saline to briny. In some areas, even shallow ground water is moderately saline. Specific constituents in parts of some aquifers in the county occur in relatively high concentrations when compared to U.S. Environmental Protection Agency drinking-water standards; for example, relatively high concentrations of sulfate, chloride, fluoride, boron, iron, manganese, and radon were found in several aquifers. The estimated mean daily water use in Carbon County in 2000 was about 320 million gallons per day. Water used for irrigation accounted for about 98 percent of this total. About 98 percent of the total water used was supplied by surface water and about 2 percent by ground water. Excluding irrigation, ground water comprised about 78 percent of total water use in Carbon County. Although ground water is used to a much lesser extent than surface water, in many areas of the county it is the only available water source.

Scientific Investigations Report↗
USGS2006

Comparison of ground-water quality in samples from selected shallow and deep wells in the central Oklahoma aquifer, 2003-2005

The aquifer units of the Central Oklahoma aquifer underlie about 2,890 square miles of central Oklahoma and are used extensively to supply water for municipal, domestic, industrial, and agricultural needs. The Central Oklahoma aquifer also is commonly referred to as the Garber-Wellington aquifer because the Garber Sandstone and Wellington Formation yield the greatest quantities of usable water for domestic and high-capacity wells. The major water-quality concerns for the Central Oklahoma aquifer described by the U.S. Geological Survey National Water Quality Assessment Program (1987 to 1992) were elevated concentrations of nitrate nitrogen in shallow water and the occurrence of arsenic, chromium, and selenium in parts of the aquifer. The quality of water from deep public-water supply wells in the Central Oklahoma aquifer is monitored by the State of Oklahoma. The chemical quality of water from shallow domestic wells is not monitored, and, therefore, there is a concern that well owners may be unknowingly ingesting water with nitrate nitrogen, arsenic, chromium, selenium, and other chemical constituents at concentrations that are considered harmful. As a result of this concern, the Oklahoma Department of Environmental Quality and the U.S. Geological Survey collaborated on a study to sample water during June 2003 through August 2005 from 23 shallow wells (less than 200 feet in depth) and 28 deep wells (200 feet or greater in depth) completed in the bedrock aquifer units of the Central Oklahoma aquifer. The objectives of the study were to describe the chemical quality of water from shallow and deep wells and to determine if the differences in constituent concentrations are statistically significant. Water from shallow wells had significantly higher concentrations of calcium, magnesium, bicarbonate, sulfate, chloride, and nitrate nitrogen than water from deep wells. There were no significant differences between concentrations of dissolved solids, sodium, and fluoride in water from shallow and deep wells. Water from 9 shallow wells had nitrate nitrogen concentrations greater than 2 milligrams per liter, suggesting nitrogen sources at land surface have had an effect on water from these wells. Water from three shallow wells (13 percent) exceeded the nitrate nitrogen maximum contaminant level of 10 milligrams per liter in drinking water. Water from shallow wells had significantly lower concentrations of arsenic, chromium, iron, and selenium than water from deep wells, whereas, concentrations of barium, copper, manganese, and zinc were similar. Water-quality data indicate that arsenic frequently occurs in shallow ground water from the Central Oklahoma aquifer, but at low concentrations (<10 micrograms per liter). The occurrence of chromium and selenium in water from shallow wells was infrequent and at low concentrations in this study. It does not appear that the quality of water from a shallow well can be predicted based on the quality of water from a nearby deep well. The results show that in general terms, shallow ground water has significantly higher concentrations of most major ions and significantly lower concentrations of arsenic, chromium, and selenium than water from deep wells.

Scientific Investigations Report↗
USGS2008

Physicochemical properties and chemical characteristics of water, bed sediment, and mussel tissue from selected streams near the Redleg and Peason Ridge impact areas, Fort Polk Military Reservation, Louisiana, June 2001 - November 2003

At the request of the U.S. Army Joint Readiness Training Center and Fort Polk, the U.S. Geological Survey collected and analyzed water, bed-sediment, and mussel-tissue samples from selected streams near the Redleg impact area (RIA) and Peason Ridge impact areas (PRIA) at the Fort Polk Military Reservation (Reservation), Louisiana. from June 2001 through November 2003. Samples were collected from 13 sites, including 2 reference sites. Water was analyzed for physicochemical properties; water and bed sediment were analyzed for major inorganic ions, cyanide, perchlorate, trace elements, total organic carbon, nutrients, and explosive compounds; and mussel tissue from three sites was analyzed for explosive compounds only. The two reference sites, one near the RIA and one near the PRIA, were selected to provide baseline data for these areas. Streams near the RIA were acidic and low in buffering capacity. with pH measurements ranging from 5.0 to 6.6. Cation concentrations were less than or equal to E3.3J mg/L (E, estimated; J, method blank contamination; milligrams per liter), and anion concentrations were less than or equal to E7.3 mg/L. Field measurements and major inorganic ions concentrations were similar to the RIA reference site and to previously sampled nearby streams, indicating streams near the RIA were typical of streams near the eastern part of the Main Post. Streams near the PRIA were slightly acidic to neutral and low in buffering capacity, with pH measurements ranging from 5.7 to 6.9. Cation concentrations were less than or equal to 6.2 mg/L, and anion concentrations were less than or equal to 16 mg/L. Streams near the PRIA were higher than the RIA for most physicochemical properties and constituents, hut typical of streams near the headwaters of the Calcasieu River. All concentrations of sulfate, chloride, and fluoride were less than the U.S. Environmental Protection Agency (USEPA) Secondary Drinking-Water Regulations (SDWR) of 250, 250, and 2.0 mg/L, respectively. Concentrations of cations calcium, magnesium. and potassium for sites near both the RIA and PRIA were higher in depositional bed-sediment samples than in bulk samples. Higher cation concentrations were likely due to higher clay and organic content in the depositional samples. The trace elements detected in the highest concentrations in water and bed sediment were aluminum, iron, and manganese. All aluminum concentrations in water were within the range or greater than the USEPA SDWR range from 50 to 200 ug/L (micrograms per liter). All but four iron concentrations in water exceeded the SDWR. Manganese concentrations in seven water samples at the RIA sites and four samples at the PRIA sites were greater than the SDWR. These concentrations of cations were consistent with soil characteristics and low pH measurements of stream water and rainfall in the area. All other trace-element concentrations in water were less than regulatory guidelines and regulations except the USEPA Maximum Contaminant Level Goal of 0 ug/L for arsenic and lead and 0.5 u/L for thallium. Arsenic, lead, and thallium concentrations were similar to those detected in blank samples or those reported for the reference sites. The Canadian Council of Ministers of the Environment (CCME) has established bed-sediment guidelines for seven trace elements: arsenic, cadmium, chromium, copper, lead, mercury, and zinc. No concentrations exceeded the CCME Probable Effect Level, and only one arsenic concentration of 8.87 mg/kg (milligrams per kilogram), in a depositional sample from one of the RIA sites, exceeded the CCME Interim Sediment Quality Guideline of 5.9 mg/kg. The median concentrations of total organic carbon in water were 5.3 mg/L at the RIA and 4.0 mg/L at the PRIA, and both concentrations were less than the average dissolved organic carbon concentration of 5.75 mg/L for all world rivers. All detected nutrient concentrations in water were less than USEPA guidelines and regulations. The largest nutrient concentrations in water and bed-sediment samples were total organic nitrogen, measured as total Kjeldahl nitrogen; they included a maximum concentration of 0.53 mg/L in water at the RIA sites, E0.38 mg/L in water at the PRIA sites, 294 mg/kg in hulk bed sediment. and 1,740 mg/kg in depositional bed sediment. Four explosive compounds, 1,3,5-trinitrobenzene, 2,4,6-trinitrotoluene, RDX (hexahydro-1,3,5-trinitro-1,3,5- triazine), and tetryl, were detected in water near the RIA; one compound, HMX (octahydro-1,3,5,7-tetranitro-1,3,5,7- tetrazocine), was detected in bed sediment near the PRIA; and one compound, nitroglycerin, was detected in mussel tissue near the RIA. The most frequently detected explosive compound, RDX, was detected in 10 water samples from 5 sites near the RIA. Concentrations of explosive compounds in water were less than USEPA Health Advisories available for reference.

Louisiana↗
USGS2008

Summary and Evaluation of the Quality of Stormwater in Denver, Colorado, October 2001 to October 2005

Stormwater in the Denver area was sampled by the U.S. Geological Survey, in cooperation with the Urban Drainage and Flood Control District, in a network of five monitoring stations - three on the South Platte River and two on tributary streams, beginning in October 2001 and continuing through October 11, 2005. Composite samples of stormwater were analyzed at the U.S. Geological Survey National Water Quality Laboratory during water years 2003-2005 and the Metro Wastewater Reclamation District Laboratory during water year 2002 for water-quality properties such as pH, specific conductance, hardness, and residue on evaporation at 105 degrees Celsius; and for constituents such as major ions (calcium, chloride, fluoride, magnesium, potassium, sodium, and sulfate) in 2005, organic carbon and nutrients, including ammonia, nitrite plus nitrate, ammonia plus organic nitrogen, phosphorus, and orthophosphate; and for metals, including total and dissolved phases of copper, lead, manganese, and zinc. Samples analyzed for bacteriological indicators such as Escherichia coli and fecal coliform collected during selected storms also were analyzed at the Metro Wastewater Reclamation Laboratory. Discrete samples collected during selected storms were analyzed at the U.S. Geological Survey National Water Quality Laboratory for a suite of water-quality properties and constituents similar to those analyzed in the composite samples but that did not include determinations for total phases of metals. Streamflow characteristics associated with 176 composite stormwater samples indicate that most samples were collected from hydrographs classified as falling or event hydrographs and that only a few samples were collected from rising hydrographs. Results from laboratory analyses of the composite samples indicate spatial patterns in which concentrations for some constituents increase with contributing drainage area in the South Platte River and Sand Creek, but no well-defined relation with the amount of urban land cover was identified using data available from the U.S. Geological Survey National Land Cover data. Results from 22 discrete samples collected during two storms and used to obtain composited results with various weighting methods indicate that correlation coefficients between time-weighted and volume-weighted concentrations were generally at least 0.65, indicating a strong direct correlation between the two weighting methods for the stations involved in this study. In addition, the central tendency for relative percent differences between the time- and volume-weighting methods typically has an absolute value of about 10 or less, indicating good agreement for these weighting methods for data collected as part of this study. Comparison of stormwater results to numeric standards for streams developed by the Colorado Department of Public Health and Environment on the basis of use classifications indicates that, for water-quality properties and constituents other than bacteriological indicators, there were very few exceptions to numeric standards. Bacteriological indicators, however, such as Escherichia coli and fecal coliform consistently exceeded numeric standards in all bacteriological samples. An evaluation of laboratory results from composite samples on the basis of annual means indicates the presence of some simple upward and downward temporal trends in concentrations. In general, for annual means of results for all stations, hardness, ammonia plus organic nitrogen, total phosphorus, most dissolved metals (lead, manganese, and zinc), and all total metals (copper, lead, manganese, and zinc) all indicate annual means that decrease each year, or downward trends. Some trends were indicated only at individual stations in the network rather than at all stations. Ammonia as nitrogen at Union, Denver, and Henderson, orthophosphate at Sand Creek, and nitrite plus nitrate at Denver and Henderson all indicate decreasing annual means, or downward tr

Scientific Investigations Report↗
USGS2009

Geochemical investigation of the Arbuckle-Simpson Aquifer, South-Central Oklahoma, 2004-06

A geochemical reconnaissance investigation of the Arbuckle-Simpson aquifer in south-central Oklahoma was initiated in 2004 to characterize the ground-water quality at an aquifer scale, to describe the chemical evolution of ground water as it flows from recharge areas to discharge in wells and springs, and to determine the residence time of ground water in the aquifer. Thirty-six water samples were collected from 32 wells and springs distributed across the aquifer for chemical analysis of major ions, trace elements, isotopes of oxygen and hydrogen, dissolved gases, and age-dating tracers. In general, the waters from wells and springs in the Arbuckle-Simpson aquifer are chemically suitable for all regulated uses, such as public supplies. Dissolved solids concentrations are low, with a median of 347 milligrams per liter (mg/L). Two domestic wells produced water with nitrate concentrations that exceeded the U.S. Environmental Protection Agency's nitrate maximum contaminant level (MCL) of 10 mg/L. Samples from two wells in the confined part of the aquifer exceeded the secondary maximum contaminant level (SMCL) for chloride of 250 mg/L and the SMCL of 500 mg/L for dissolved solids. Water samples from these two wells are not representative of water samples from the other wells and springs completed in the unconfined part of the aquifer. No other water samples from the Arbuckle-Simpson geochemical reconnaissance exceeded MCLs or SMCLs, although not every chemical constituent for which the U.S. Environmental Protection Agency has established a MCL or SMCL was analyzed as part of the Arbuckle-Simpson geochemical investigation. The major ion chemistry of 34 of the 36 samples indicates the water is a calcium bicarbonate or calcium magnesium bicarbonate water type. Calcium bicarbonate water type is found in the western part of the aquifer, which is predominantly limestone. Calcium magnesium bicarbonate water is found in the eastern part of the aquifer, which is predominantly a dolomite. The major ion chemistry for these 34 samples is consistent with a set of water-rock interactions. Rainfall infiltrates the soil zone, where the host rock, limestone or dolomite, dissolves as a result of uptake of carbon dioxide gas. Some continued dissolution of dolomite and precipitation of calcite occur as the water flows through the saturated zone. The major ion chemistry of the two samples from wells completed in the confined part of the aquifer indicates the water is a sodium chloride type. Geochemical inverse modeling determined that mixing of calcite-saturated recharge water with brine and dissolving calcite, dolomite, and gypsum accounts for the water composition of these two samples. One of the two samples, collected at Vendome Well in Chickasaw National Recreation Area, had a mixing fraction of brine of about 1 percent. The brine component of the sample at Vendome Well is likely to account for the relatively large concentrations of many of the trace elements (potassium, fluoride, bromide, iodide, ammonia, arsenic, boron, lithium, selenium, and strontium) measured in the water sample. Carbon-14, helium-3/tritium, and chlorofluorocarbons were used to calculate ground-water ages, recharge temperatures, and mixtures of ground water in the Arbuckle-Simpson aquifer. Thirty four of 36 water samples recharged the aquifer after 1950, indicating that water is moving quickly from recharge areas to discharge at streams and springs. Two exceptions to this classification were noted in samples 6 and 15 (Vendome Well). Ground-water ages determined for these two samples by using carbon-14 are 34,000 years (site 6) and 10,500 years (site 15). Concentrations of dissolved argon, neon, and xenon in water samples were used to determine the temperature of the water when it recharged the aquifer. The mean annual air temperature at Ada, Oklahoma, is 16 degrees Celsius (C) and the median temperature of the 30 reconnaissance water samples was 18.1 C. The av

Oklahoma↗
USGS2009

Factors Affecting Water Quality in Domestic Wells in the Upper Floridan Aquifer, Southeastern United States, 1998-2005

The Floridan aquifer system is a highly productive carbonate aquifer that provides drinking water to about 10 million people in Florida, Georgia, and South Carolina. Approximately 1.6 million people rely on domestic wells (privately owned household wells) for drinking water. Withdrawals of water from the Floridan aquifer system have increased by more than 500 percent from 630 million gallons per day (2.38 cubic meters per day) in 1950 to 4,020 million gallons per day (15.2 cubic meters per day) in 2000, largely due to increases in population, tourism, and agriculture production. Water samples were collected from 148 domestic wells in the Upper Floridan aquifer in Florida, Georgia, South Carolina, and Alabama during 1998-2005 as part of the U.S. Geological Survey (USGS) National Water-Quality Assessment Program. The wells were located in different hydrogeologic settings based on confinement of the Upper Floridan aquifer. Five networks of wells were sampled con-sisting of 28 to 30 wells each: two networks were in unconfined areas, two networks were in semiconfined areas, and one network was in the confined area. Physical properties and concentrations of major ions, trace elements, nutrients, radon, and organic compounds (volatile organic compounds and pesticides) were measured in water samples. 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). The MCL for fluoride of 4 milligrams per liter (mg/L) was exceeded for two samples (about 1 percent of samples). A proposed MCL for radon of 300 picocuries per liter was exceeded in about 40 percent of samples. Nitrate concentrations in the Upper Floridan aquifer ranged from less than the laboratory reporting level of 0.06 to 8 mg/L, with a median nitrate concentration less than 0.06 mg/L (as nitrogen). Nitrate concentrations did not exceed the MCL of 10 mg/L. Statistical comparisons indicated that median nitrate concentrations were significantly different by degree of confinement where the highest median nitrate concentration was 1.46 mg/L for 58 samples from unconfined areas, and by network, where the highest median nitrate concentration was 2.43 mg/L in 28 samples from unconfined areas in southwestern Georgia. Nitrate concentrations in unconfined areas were positively correlated to: (1) the percentage of agricultural land use around the well, (2) the amount of nitrogen fertilizer applied, and (3) the dissolved oxygen concentrations in groundwater. Volatile organic compounds (VOCs) were detected in about 63 percent of all samples. Chloroform, carbon disulfide, and 1,2-dichloropropane were the most frequently detected VOCs. Chloroform, a byproduct of water chlorination, was most frequently detected in unconfined urban areas. Carbon disulfide, a solvent, was most frequently detected in confined areas in southeastern Georgia. Pesticides were detected in about 21 percent of all samples, but were detected in about 69 percent of the 28 samples from unconfined areas in southwestern Georgia. The herbicides atrazine, deethylatrazine, and metolachlor were the most frequently detected pesticides.

Scientific Investigations Report↗