USGS Science⌕ Search

SEARCH · USGS Science

Results for “Chemical Geology”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 847 records · Page 47Linked to original sources
USGS1997

Physical and chemical characteristics of Terrace Reservoir, Conejos County, Colorado, May 1994 through May 1995

Terrace Reservoir receives drainage of low-pH, metal-enriched water from mineralized areas, including the Summitville Mine, within the Alamosa River Basin. Drainage from the Summitville Mine has contributed a substantial part of the metal load to Terrace Reservoir. From May 1994 through May 1995, a study was done by the U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, to evaluate the physical and chemical characteristics of Terrace Reservoir. Terrace Reservoir was thermally stratified from about mid-May through August 1994. Thermal stratification was absent from September\x111994through March 1995. During periods of stratification, underflow of the Alamosa River was predominant, and residence times of the underflow were shortened by 40 to 75\x11percent of the theoretical residence times for a well-mixed reservoir. Transport and deposition of suspended solids in Terrace Reservoir varied spatially and temporally. Most of the suspended solids were deposited in Terrace Reservoir. The concentration of dissolved oxygen in the reservoir varied little spatially or temporally and generally was within a few tenths of the dissolved-oxygen concentration of the inflow. The pH of water in the reservoir generally ranged from about 4.0 to about 7.0, depending on date, depth, and location. The largest pH values were measured during May. A markeddecrease of about 1.5\x11pH units occurred at site T5 in the reservoir about mid-June. The pH of the reservoir remained at or below 5.5 from mid-June through November. Dissolved-metal concentrations varied spatially and temporally in response to several factors, which included inflow characteristics, reservoir stratification and mixing, inflow-routing and flow-through patterns, residence times, sedimentation, dissolved oxygen, and pH.Inflow chemistry is the dominant controlling factor of metal chemistry within Terrace Reservoir.During periods of stratification, large vertical variations in metal concentrations occurred. The highest metal concentrations in the reservoir generally were measured in the hypolimnion between June and August. During June, epilimnetic water of the reservoir had pH values greater than 6.0, and metal concentrations were lower than hypolimnetic concentrations. In the hypolimnion, pH values were less than 5.5. The difference between the chemistry of the epilimnion and the hypolimnion was due to differences in flow routing and residence times of water in those respective layers. The dissolved-metal concentrations were larger during July and August than during June.During September, small vertical variations in metalconcentrations occurred, and the dissolved-metal concentrations were nearly equivalent to the average August metal concentrations, indicatingthat the metal concentrations measured during September resulted largely from reservoir mixing.During March, the largest metal concentrationsoccurred in the epilimnion, where pH was about 5.5; in the hypolimnion, where the pH was about 6.0, dissolved-metal concentrations were substantially lower and reflected inflow concentrations.

Colorado↗
USGS2007

A simple scheme to determine potential aquatic metal toxicity from mining wastes

A decision tree (mining waste decision tree) that uses simple physical and chemical tests has been developed to determine whether effluent from mine waste material poses a potential toxicity threat to the aquatic environment. For the chemical portion of the tree, leaching tests developed by the United States Geological Survey, the Colorado Division of Minerals and Geology (Denver, CO), and a modified 1311 toxicity characteristic leaching procedure (TCLP) test of the United States Environmental Protection Agency have been extensively used as a surrogate for readily available metals that can be released into the environment from mining wastes. To assist in the assessment, element concentration pattern graphs (ECPG) are produced that compare concentrations of selected groups of elements from the three leachates and any water associated with the mining waste. The MWDT makes a distinction between leachates or waters with pH less than or greater than 5. Generally, when the pH values are below 5, the ECPG of the solutions are quite similar, and potential aquatic toxicity from cationic metals, such as Pb, Cu, Zn, Cd, and Al, is assumed. Below pH 5, these metals are mostly dissolved, generally are not complexed with organic or inorganic ligands, and hence are more bioavailable. Furthermore, there is virtually no carbonate alkalinity at pH less than 5. All of these factors promote metal toxicity to aquatic organisms. On the other hand, when the pH value of the water or the leachates is above 5, the ECPG from the solutions are variable, and inferred aquatic toxicity depends on factors in addition to the metals released from the leaching tests. Hence, leachates and waters with pH above 5 warrant further examination of their chemical composition. Physical ranking criteria provide additional information, particularly in areas where waste piles exhibit similar chemical rankings. Rankings from physical and chemical criteria generally are not correlated. Examples of how this decision tree has been applied in assessing mine sites are discussed. Copyright ?? Taylor & Francis Group, LLC.

Conference Paper↗
USGS2006

Hydrogeochemical investigations in the Osgood Mountains, north-central Nevada

Field investigations performed in the Osgood Mountains during the summers of 1999 and 2000 were designed to test methods of combining geologic, hydrologic, and geochemical investigations. The goals were to develop a more thorough understanding of the movement of water through the study area and to understand the water-rock reactions that may occur along flow paths. The Osgood Mountains were chosen for study because they represent a well-defined geologic system, based on existing and new field data. New work in the area focused on gathering more data about fractures, faults, and joints and on collecting water samples to evaluate the role of geologic structures on hydrologic and geochemical properties of the ground-water/surface-water system. Chemical methods employed in the study included measuring traditional field parameters (e.g., pH, temperature, conductivity, dissolved oxygen) as well as Fe2+ and collecting a variety of samples that were preserved for later laboratory analysis. Hydrologic methods included closely spaced evaluations of substream hydraulic head to define ground-water discharge and recharge zones as well as some measurements of stream discharge. Geologic investigations focused on the locations and orientations of fractures and kinematic indicators of slip observable in outcrops.

Nevada↗
USGS2014

A 19-year record of chemical and isotopic composition of water from springs of the Shenandoah National Park, Virginia, 1995-2014

During October 1995 through March 2014, the U.S. Geological Survey in cooperation with the National Park Service, Luray, Virginia Station collected and analyzed samples of selected springs, air and unsaturated-zone gases in Shenandoah National Park, Virginia. The 19-year record of measurements of chemical and isotopic composition of water discharging from 34 springs located along the crest of the Blue Ridge Mountains in Shenandoah National Park, Virginia, is reported. These data include field measurements of water temperature, specific conductance, concentrations of dissolved oxygen (O 2 ), and pH. Laboratory measurements included major-, minor-, and trace-element chemistry; concentrations of dissolved gases (nitrogen, [N 2 ] argon [Ar], oxygen, and carbon dioxide [CO 2 ]); concentrations of dissolved trace atmospheric gases, including trichlorofluoromethane (CFC-11), dichlorodifluoromethane (CFC-12), and trichlorotrifluoroethane (CFC-113) and sulfur hexafluoride (SF 6 ); and hydrogen stable isotopic composition (δ 2 H) and oxygen isotopic composition (δ 18 O) of water. The data include an up to 14-year time series record of monthly sampling at five springs collected between 1995 and 2013. The measurements included temperature, specific conductance, pH, and discharge recorded at 30-minute intervals. Atmospheric mixing ratios of CFC-11, CFC-12, CFC-113, trifluorobromomethane (CF 3 Br), SF 6 , and trifluoromethyl sulfur pentafluoride (SF 5 CF 3 ) in air from the Big Meadows Air Monitoring Station, Shenandoah National Park, were measured at approximately weekly intervals from September 1995 through March 2014. Additional data include monthly (between May 2001 and August 2003) measurements of temperature, N 2 , O 2 , Ar, CO 2 , CFC-12, CFC-11, CFC-113, and SF 6 concentrations in unsaturated-zone air from seven multilevel piezometers in Shenandoah National Park and at the U.S. Geological Survey National Center in Reston, Virginia. All samples were analyzed at the U.S. Geological Survey Laboratories in Reston, Virginia.

Virginia↗
USGS1996

Physical and chemical characteristics of Terrace Reservoir, Conejos County, Colorado, May 1994 through May 1995; interim report

Terrace Reservoir receives drainage of low-pH, metal-enriched water from mineralized areas, including the Summitville Mine, within the Alamosa River Basin. Drainage from the Summitville Mine has contributed a substantial part of the metal load to Terrace Reservoir. From May 1994 through May 1995, a study was done by the U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, to evaluate the physical and chemical characteristics of Terrace Reservoir. Terrace Reservoir was thermally stratified from about mid-May through August 1994. Thermal stratification was absent from September\x111994through March 1995. During periods of stratification, underflow of the Alamosa River was predominant, and residence times of the underflow were shortened by 40 to 75\x11percent of the theoretical residence times for a well-mixed reservoir. Transport and deposition of suspended solids in Terrace Reservoir varied spatially and temporally. Most of the suspended solids were deposited in Terrace Reservoir. The concentration of dissolved oxygen in the reservoir varied little spatially or temporally and generally was within a few tenths of the dissolved-oxygen concentration of the inflow. The pH of water in the reservoir generally ranged from about 4.0 to about 7.0, depending on date, depth, and location. The largest pH values were measured during May. A markeddecrease of about 1.5\x11pH units occurred at site T5 in the reservoir about mid-June. The pH of the reservoir remained at or below 5.5 from mid-June through November. Dissolved-metal concentrations varied spatially and temporally in response to several factors, which included inflow characteristics, reservoir stratification and mixing, inflow-routing and flow-through patterns, residence times, sedimentation, dissolved oxygen, and pH. Inflow chemistry is the dominant controlling factor of metal chemistry within Terrace Reservoir. During periods of stratification, large vertical variations in metal concentrations occurred. The highest metal concentrations in the reservoir generally were measured in the hypolimnion between June and August. During June, epilimnetic water of the reservoir had pH values greater than 6.0, and metal concentrations were lower than hypolimnetic concentrations. In the hypolimnion, pH values were less than 5.5. The difference between the chemistry of the epilimnion and the hypolimnion was due to differences in flow routing and residence times of water in those respective layers. The dissolved-metal concentrations were larger during July and August than during June. During September, small vertical variations in metal concentrations occurred, and the dissolved-metal concentrations were nearly equivalent to the average August metal concentrations, indicatingthat the metal concentrations measured during September resulted largely from reservoir mixing.During March, the largest metal concentrationsoccurred in the epilimnion, where pH was about 5.5; in the hypolimnion, where the pH was about 6.0, dissolved-metal concentrations were substantially lower and reflected inflow concentrations.

Colorado↗
USGS2018

Hydrology-driven chemical loads transported by the Green River to the Lower Duwamish Waterway near Seattle, Washington, 2013–17

The sediments in the Lower Duwamish Waterway Superfund site in Seattle, Washington, are contaminated with chemicals including metals such as arsenic, polychlorinated biphenyls (PCBs), carcinogenic polycyclic aromatic hydrocarbons (cPAHs), and dioxins/furans from decades of intense anthropogenic activities. The U.S. Geological Survey, in cooperation with the Washington State Department of Ecology, collected new data from 2013 to 2017 to estimate sediment and chemical loads transported by the Green/Duwamish River to the Lower Duwamish Waterway Superfund site (the final 8-kilometer reach of the river) in support of sediment remediation within the site. Chemical loads were calculated as the product of river suspended-sediment loads and suspended sediment-bound chemical concentrations measured at river kilometer 16.7. Using four different approaches, annual suspended sediment-bound chemical load estimates transported by the river to the Lower Duwamish Waterway were in the range of 1,120–1,470 kilograms arsenic, 2,810–8,200 grams (g) toxic equivalent cPAHs, 205–407 milligrams toxic equivalent dioxins/furans, and 340–1,180 g PCBs. Storm events contributed a disproportionately large amount of the load of anthropogenic organic compounds such as cPAHs (54 percent), dioxins/furans (44 percent), and PCBs (52 percent) as compared to overall time (17 percent). Chemical concentrations and load estimates often were underestimated using results from unfiltered water analysis only, especially in samples with high suspended-sediment concentrations and for hydrophobic organic chemicals such as cPAHs that prefer to sorb to particulates and are at low concentrations near or below the analytical limits of water methods. For metals and PCBs, the dissolved concentration was relatively low and consistent between sampling events, whereas the suspended sediment-bound chemical concentrations contributed most of the chemical concentration in the water column during periods of high river suspended-sediment concentrations. However, the dissolved fraction, on average, contributed more than one-third of the estimated total chemical load in the river system for arsenic and PCBs, even given the hydrophobic nature of the chemicals. These results suggest that the sum of the chemical concentrations measured on two separate fractions—the particulate fraction and the dissolved fraction—more fully represents the total chemical concentration as compared to analysis of an unfiltered water sample, especially in samples with high suspended-sediment concentrations. Most of the suspended-sediment load (97 percent) and sediment-bound chemical load (92–94 percent) occurred during the wet winter half of the year from October 15 to April 14. However, the highest sediment-bound chemical concentrations often occurred during short intense storms or “first flush” autumn runoff events during the dry summer half of the year from April 15 to October 14. Because of the highly variable and dynamic river system characteristics (including precipitation, discharge, sediment concentration, and tidal fluctuations), it is critical to characterize the occurrence, frequency, concentrations, and loads during extreme conditions (for example, when the river is affected by storm-derived runoff) rather than time-averaged conditions. These short extreme events have a high potential for acute effects on ecological and human health, and may have a great influence on the effectiveness of the sediment remediation activities that are underway in the Lower Duwamish Waterway.

Washington↗
USGS1965

Records of wells and test holes, materials tests, and chemical analyses of water in the Assabet River basin, Massachusetts

The Assabet River, located in Worcester and Middlesex Counties in eastern Massachusetts, drains an area of approximately 177 square miles. The area includes all or a portion of the following towns: Acton, Boxborough, Carlisle, Concord, Hudson, Littleton, Marlborough, Maynard, Stow, Sudbury, and Westford in Middlesex County; Berlin, Bolton, Boylston, Clinton, Grafton, Harvard, Northborough, Shrewsbury, and Westborough in Worcester County (see plate 1 in pocket). This report presents data collected as part of an investigation of the ground-water resources in the Assabet River basin by the U.S. Geological Survey in cooperation with the Massachusetts Water Resources Commission. The data have been prepared for release in order to make available to the public basic ground-water data that will be useful in the planning of water-resources development. The data in this report were collected intermittently from 1939 to 1964 by H. A. Wilde, H. L. Pree, H. N. Halberg, J. A. Baker, R. W. Macomber, W. B. Fleck, and S. J. Pollock. The selected data in tables 2, 3, 4, and 5 represent those wells, test wells, and borings that were deemed representative of any given location. Data of some one hundred wells and test wells and over one thousand bridge and roadway borings are not included in this report, but may be inspected at the U.S. Geological Survey, Ground Water Branch, 211 Congress Street, Boston, Massachusetts. Tables 6-9 include data on chemical analyses of water samples, physical and hydrologic properties of materials samples, and water-table measurements made during the years 1961 through 1964. The geologic units used in tables 2 and 3 are described in table 1.

Massachusetts↗
USGS1990

Records of wells and chemical analyses of ground water in Deuel and Hamlin counties, South Dakota

Well and chemical groundwater data contained in three tables were collected during a 5-year study started in 1971 to determine the geology and water resources of Deuel and Hamlin Counties, South Dakota. Physical, hydrologic, and geologic data for 3,228 wells and test holes have been entered into computer storage in the Ground-Water Site Inventory File of the U.S. Geological Survey 's National Water Data Storage and Retrieval System (WATSTORE). The well tables in the report are computer printouts from WATSTORE. Water quality data from 564 chemical analyses have been stored in the Water-Quality File of WATSTORE and is computer printed in the chemical analyses table by aquifer. (USGS)

Open-File Report↗
USGS1963

Geologic and hydrologic features of the San Bernardino area, California; with special reference to underflow across the San Jacinto fault

This is the second in a series of interpretive reports on subsurface outflow from the ground-water basins of San Bernardino County, Calif., prepared by the U.S. Geological Survey in cooperation with the San Bernardino County Flood Control District. One principal purpose of the study was to estimate the ground-water outflow from the Bunker Hill basin to the Rialto-Colton basin across the San Jacinto fault, which, except locally, forms a nearly impermeable boundary between the two basins. In addition, the report deals qualitatively with the geology, the fault barriers that divide the area into several ground-water basins, the physical nature and degree of imperviousness of the barriers, the occurrence and movement of ground water and fluctuations of water level in the basins, and the chemical quality of surface and ground waters in the San Bernardino area. The report includes a geologic map and sections, water-level-contour maps and profiles, and hydrographs of selected well. The Santa Ana River, the principal stream, flows generally westward across the area. Channels of the river and its tributaries overlie a large irregular structural depression filled with alluvial deposits ranging in age from late Tertiary to Recent and forming a valley bounded on the north by the San Gabriel Mountains, on the east by the San Bernardino Mountains, and on the south by an irregular group of hills. Large alluvial fans underlie most of the area, but its landforms also include alluvial benches and terraces near the mountains, stream channels, and elongate hills, ridges, and scarps along the trace of the San Jacinto fault, which strikes northwestward across the valley about in the center of the area. This fault and others divide the area into ground-water basins, which include the Bunker Hill, Rialto-Colton, upper and lower Lytle and Chino basins. The water-bearing deposits include the following units: the younger alluvium. of Recent age, which occupies principally the backfilled channels beneath the Santa Ana River and its tributaries and through which ground water moves from Bunker Hill basin to Rialto-Colton basin; the older alluvium, of Pleistocene age, which is the principal water-bearing unit of the area and yields water to more than a thousand wells; and continental deposits of Tertiary to Quaternary age, which crop out along the southern margin of the area and locally along the San Gabriel Mountains on the north. The younger alluvium attains a maximum thickness of about 125 feet beneath the Santa Ana River south of San Bernardino. Locally in the Bunker Hill basin it is composed of two members, an upper member of relatively impermeable clay and a lower member of highly permeable material in which water is confined by the upper member. The older alluvium locally has a known thickness greater than 700 feet; elsewhere in the San Bernardino Valley it may exceed 1,400 feet. Locally, where ground water is confined in Bunker Hill basin, the older alluvium is divided into three permeable water-bearing zones separated from each other and from the younger alluvium above by less permeable zones. In parts of Chino and Rialto-Colton basins the alluvium consists of a coarse-grained facies along a former course of a major stream that is interfingered with and overlain by relatively fine-grained deposits. The permeability of the younger alluvium in the area beneath the Santa Ana River downstream from the San Jacinto fault was determined from tests to be about 2,700 gallons per day per square foot. The permeability of the coarse water-yielding materials of the older alluvium several miles downstream was estimated from tests to be about the same magnitude. Rocks that yield practically no water include continental rocks of Tertiary age, which are not exposed in the area but are tapped by wells in Rialto-Colton basin, and crystalline and metamorphic rocks of pre-Tertiary age that form the bedrock of the area.

California↗
USGS1971

Summary of data on chemical quality of streams of North Carolina, 1943-67

This report summarizes water-quality data collected by the U.S. Geological Survey in cooperation with the State of North Carolina during the period 1943-67. Maximum, minimum, and average values are shown for complete analyses of mineral constituents dissolved in water from 177 locations at which samples were collected daily or monthly for at least 1 consecutive year. Maximum and minimum values are given for 460 'miscellaneous and occasional stations' at which two or more chemical analyses were made. Single analyses are shown for 580 additional sampling sites. A total of about 19,000 analyses were used in determining statistical values included in the report. Water in streams of North Carolina is generally of good mineral quality and is acceptable with a minimum amount of treatment for most uses.

North Carolina↗
USGS2015

Simulation of the effects of different inflows on hydrologic conditions in Lake Houston with a three-dimensional hydrodynamic model, Houston, Texas, 2009–10

Lake Houston, an important water resource for the Houston, Texas, area, receives inflows from seven major tributaries that compose the San Jacinto River Basin upstream from the reservoir. The effects of different inflows from the watersheds drained by these tributaries on the residence time of water in Lake Houston and closely associated physical and chemical properties including lake elevation, salinity, and water temperature are not well known. Accordingly, the U.S. Geological Survey (USGS), in cooperation with the City of Houston, developed a three-dimensional hydrodynamic model of Lake Houston as a tool for evaluating the effects of different inflows on residence time of water in the lake and associated physical and chemical properties. The Environmental Fluid Dynamics Code (EFDC), a grid-based, surface-water modeling package for simulating three-dimensional circulation, mass transport, sediments, and biogeochemical processes, was used to develop the model of Lake Houston. The Lake Houston EFDC model was developed and calibrated by using 2009 data and verified by using 2010 data. Three statistics (mean error, root mean square error, and the Nash-Sutcliffe model efficiency coefficient) were used to evaluate how well the Lake Houston EFDC model simulated lake elevation, salinity, and water temperature. The residence time of water in reservoirs is associated with various physical and chemical properties (including lake elevation, salinity, and water temperature). Simulated and measured lake-elevation values were compared at USGS reservoir station 08072000 Lake Houston near Sheldon, Tex. The accuracy of simulated salinity and water temperature values was assessed by using the salinity (computed from measured specific conductance) and water temperature at two USGS monitoring stations: 295826095082200 Lake Houston south Union Pacific Railroad Bridge near Houston, Tex., and 295554095093401 Lake Houston at mouth of Jack’s Ditch near Houston, Tex. Specific conductance and water temperature were measured at as many as four different depths at each of the two monitoring stations during 2009 and then used for assessing the accuracy of simulated values of salinity and water temperature during 2010. The performance evaluation statistics indicate that the model performed satisfactorily. The calibrated model was used to simulate two possible inflow scenarios to evaluate the changes in the residence time of water in Lake Houston. The two scenarios tested were an increased inflow of approximately 300 cubic feet per second for 1 month (May 2010) from two watersheds: the West Fork San Jacinto River and Luce Bayou. These scenarios were chosen to mimic the effects of possible small releases or diversions of water from outside the San Jacinto River Basin into the basin (or directly into the lake) on the residence time of water in Lake Houston. During the time of increased inflow for the two scenarios tested, maximum residence time decreased slightly from approximately 106 to 97 days.

Texas↗
USGS1975

Chemical and biological quality of water in part of the Everglades, southeastern Florida

A comprehensive monitoring network was established in a part of the Everglades to evaluate the quality of water being delivered to Everglades National Park. Physical, chemical, and biological parameters were determined in surface water, bottom sediment, and bulk precipitation (rainfall and dry fallout). The geology of the area, bottom sediment, bulk precipitation, natural, urban, and agricultural runoff, and the characteristics of the hydrologic system in the Everglades influence the type and concentration of each chemical constituent and how it affects the water quality. The quality of surface water in the agricultural area between Lake Okeechobee and the water conservation areas is markedly different from that of other surface water in southeastern Florida. In general, the water in this area is higher in concentrations of most chemical constituents. Man has engaged in cultural activities, both agricultural and urban, which have affected the water quality in the northern and eastern segments of the area of investigation. The quality of the water improves, however, as it flows to the south and east because there is minimal input from man's activities and many of the constituents are assimilated by plants, sorbed on organic material and clay in the bottom sediments, and entrapped within the sediments. Dilution by rainfall and concentration by evapotranspiration are also important factors that influence the quality of surface water in the area of investigation. The area of investigation in the Everglades is a sink for macronutrients, trace metals, and chlorinated-hydrocarbon insecticides. These constituents do not move through the system freely. They become tied up in various complexes and for that reason, the water being delivered to Everglades National Park is of better quality than the water entering the northern edge of the water conservation areas. The various physical and biological processes and chemical reactions combine to improve the water quality as the water flows southward. The data presented in this report may be used as a baseline for determination of future changes in water quality at the several places in the Everglades where recurrent sampling of rainfall, surface water, and bottom sediments was undertaken during the course of the investigation.

Florida↗
USGS2007

Simulation of Multiscale Ground-Water Flow in Part of the Northeastern San Joaquin Valley, California

The transport and fate of agricultural chemicals in a variety of environmental settings is being evaluated as part of the U.S. Geological Survey (USGS) National Water-Quality Assessment Program. One of the locations being evaluated is a 2,700-km2 (square kilometer) regional study area in the northeastern San Joaquin Valley surrounding the city of Modesto, an area dominated by irrigated agriculture in a semi-arid climate. Ground water is a key source of water for irrigation and public supply, and exploitation of this resource has altered the natural flow system. The aquifer system is predominantly alluvial, and an unconfined to semiconfined aquifer overlies a confined aquifer in the southwestern part of the study area; these aquifers are separated by the lacustrine Corcoran Clay. A regional-scale 16-layer steady-state model of ground-water flow in the aquifer system in the regional study area was developed to provide boundary conditions for an embedded 110-layer steady-state local-scale model of part of the aquifer system overlying the Corcoran Clay along the Merced River. The purpose of the local-scale model was to develop a better understanding of the aquifer system and to provide a basis for simulation of reactive transport of agricultural chemicals. The heterogeneity of aquifer materials was explicitly incorporated into the regional and local models using information from geologic and drillers? logs of boreholes. Aquifer materials were differentiated in the regional model by the percentage of coarse-grained sediments in a cell, and in the local model by four hydrofacies (sand, silty sand, silt, and clay). The calibrated horizontal hydraulic conductivity values of the coarse-grained materials in the zone above the Corcoran Clay in the regional model and of the sand hydrofacies used in the local model were about equal (30?80 m/d [meter per day]), and the vertical hydraulic conductivity values in the same zone of the regional model (median of 0.012 m/d), which is dominated by the finer-grained materials, were about an order of magnitude less than that for the clay hydrofacies in the local model. Data used for calibrating both models included long-term hourly water-level measurements in 20 short-screened wells installed by the USGS in the Modesto and Merced River areas. Additional calibration data for the regional model included water-level measurements in 11 wells upslope and 17 wells downslope from these areas. The root mean square error was 2.3 m (meter) for all wells in the regional model and 0.8 m for only the USGS wells; the associated average errors were 0.9 m and 0.3 m, respectively. The root mean square error for the 12 USGS wells along a transect in the local model area was 0.08 m; the average error was 0.0 m. Particle tracking was used with the local model to estimate the concentration of an environmental tracer, sulfur hexafluoride, in 10 USGS transect wells near the Merced River that were sampled for this constituent. Measured and estimated concentrations in the mid-depth and deepest wells, which would be most sensitive to errors in hydraulic conductivity estimates, were consistent. The combined results of particle tracking and sulfur hexafluoride analysis suggest that most water sampled from the transect wells was recharged less that 25 years ago.

Scientific Investigations Report↗
USGS1986

Records of wells and chemical analyses of ground water in Brown County, South Dakota

Well and chemical groundwater data contained in two tables were collected during a 5-year study started in 1967 to determine the geology and water resources of Brown County, South Dakota. Physical, hydrologic, and geologic data for 3,127 wells and test holes have been entered into computer storage in the Ground-Water Site Inventory File of the U.S. Geological Survey 's National Water Data Storage and Retrieval System (WATSTORE). The well table in the report is a computer printout from WATSTORE. Water quality data from 750 chemical analyses has been stored in the Water-Quality File of WATSTORE and is computer printed in the chemical analyses table by aquifer. (USGS)

Open-File Report↗
USGS1987

Records of wells and chemical analyses of ground water in Campbell County, South Dakota

Well and chemical groundwater data contained in two tables were collected during a 3-yr study started in 1964 to determine the geology and water resources of Campbell County, South Dakota. Physical, hydrologic, and geologic data for 631 wells and test holes have been entered into computer storage in the Groundwater Site Inventory File of the U.S. Geological Survey 's National Water Data Storage and Retrieval System (WATSTORE). The well table in the report is a computer printout from WATSTORE. Water quality data from 257 chemical analyses have been stored in the Water Quality File of WATSTORE and is computer printed in the chemical table by aquifer. (USGS)

Open-File Report↗
USGS2009

Occurrence and distribution of fecal indicator bacteria, and physical and chemical indicators of water quality in streams receiving discharge from Dallas/Fort Worth International Airport and vicinity, North-Central Texas, 2008

This report, done by the U.S. Geological Survey in cooperation with Dallas/Fort Worth International (DFW) Airport in 2008, describes the occurrence and distribution of fecal indicator bacteria (fecal coliform and Escherichia [E.] coli), and the physical and chemical indicators of water quality (relative to Texas Surface Water Quality Standards), in streams receiving discharge from DFW Airport and vicinity. At sampling sites in the lower West Fork Trinity River watershed during low-flow conditions, geometric mean E. coli counts for five of the eight West Fork Trinity River watershed sampling sites exceeded the Texas Commission on Environmental Quality E. coli criterion, thus not fully supporting contact recreation. Two of the five sites with geometric means that exceeded the contact recreation criterion are airport discharge sites, which here means that the major fraction of discharge at those sites is from DFW Airport. At sampling sites in the Elm Fork Trinity River watershed during low-flow conditions, geometric mean E. coli counts exceeded the geometric mean contact recreation criterion for seven (four airport, three non-airport) of 13 sampling sites. Under low-flow conditions in the lower West Fork Trinity River watershed, E. coli counts for airport discharge sites were significantly different from (lower than) E. coli counts for non-airport sites. Under low-flow conditions in the Elm Fork Trinity River watershed, there was no significant difference between E. coli counts for airport sites and non-airport sites. During stormflow conditions, fecal indicator bacteria counts at the most downstream (integrator) sites in each watershed were considerably higher than counts at those two sites during low-flow conditions. When stormflow sample counts are included with low-flow sample counts to compute a geometric mean for each site, classification changes from fully supporting to not fully supporting contact recreation on the basis of the geometric mean contact recreation criterion. All water temperature measurements at sampling sites in the lower West Fork Trinity River watershed were less than the maximum criterion for water temperature for the lower West Fork Trinity segment. Of the measurements at sampling sites in the Elm Fork Trinity River watershed, 95 percent were less than the maximum criterion for water temperature for the Elm Fork Trinity River segment. All dissolved oxygen concentrations were greater than the minimum criterion for stream segments classified as exceptional aquatic life use. Nearly all pH measurements were within the pH criterion range for the classified segments in both watersheds, except for those at one airport site. For sampling sites in the lower West Fork Trinity River watershed, all annual average dissolved solids concentrations were less than the maximum criterion for the lower West Fork Trinity segment. For sampling sites in the Elm Fork Trinity River, nine of the 13 sites (six airport, three non-airport) had annual averages that exceeded the maximum criterion for that segment. For ammonia, 23 samples from 12 different sites had concentrations that exceeded the screening level for ammonia. Of these 12 sites, only one non-airport site had more than the required number of exceedances to indicate a screening level concern. Stormflow total suspended solids concentrations were significantly higher than low-flow concentrations at the two integrator sites. For sampling sites in the lower West Fork Trinity River watershed, all annual average chloride concentrations were less than the maximum annual average chloride concentration criterion for that segment. For the 13 sampling sites in the Elm Fork Trinity River watershed, one non-airport site had an annual average concentration that exceeded the maximum annual average chloride concentration criterion for that segment.

Scientific Investigations Report↗
USGS1993

Climatic impact on isovolumetric weathering of a coarse-grained schist in the northern Piedmont Province of the central Atlantic states

The possible impact of periglacial climates on the rate of chemical weathering of a coarse-grained plagioclase-muscovite-quartz schist has been determined for a small watershed near Baltimore, Maryland. The isovolumetric chemical weathering model formulated from the geochemical mass balance study of the watershed shows that the weathering front advances at a velocity of 9.1 m/m.y., if the modern environmental parameters remain the same back through time. However, recent surficial geological mapping demonstrates that periglacial climates have impacted the area. Such an impact significantly affects two key chemical weathering parameters, the concentration of CO 2 in the soil and groundwater moving past the weathering front. Depending upon the assumptions used in the model, the rate of saprolitization varies from 2.2 to 5.3 m/m.y. The possible impact of periglacial processes suggested by the chemical weathering rates indicates a need to reconsider theories of landscape evolution as they apply to the northern Piedmont Province of the mid-Atlantic states. I suggest that from the Late Miocene to the present that the major rivers have become incised in their present locations; this incision has enhanced groundwater circulation and chemical weathering such that crystalline rocks beneath interfluvial areas remain mantled by saprolite; and the saprolite mantle has been partially stripped as periglacial conditions alternate with humid-temperate conditions.

Geomorphology↗
USGS2013

U.S. Geological Survey environmental health science strategy — Providing environmental health science for a changing world

Executive Summary America has an abundance of natural resources. We have bountiful clean water, fertile soil, and unrivaled national parks, wildlife refuges, and public lands. These resources enrich our lives and preserve our health and wellbeing. These resources have been maintained because of our history of respect for their value and an enduring commitment to their vigilant protection. Awareness of the social, economic, and personal value of the health of our environment is increasing. The emergence of environmentally driven diseases caused by exposure to contaminants and pathogens is a growing concern worldwide. New health threats and patterns of established threats are affected by both natural and anthropogenic changes to the environment. Human activities are key drivers of emerging (new and re-emerging) health threats. Societal demands for land and natural resources, quality of life, and economic prosperity lead to environmental change. Natural earth processes, climate trends, and related climatic events will compound the environmental impact of human activities. These environmental drivers will influence exposure to disease agents, including viral, bacterial, prion, and fungal pathogens, parasites, synthetic chemicals and substances, natural earth materials, toxins, and other biogenic compounds. The U.S. Geological Survey (USGS) defines environmental health science broadly as the interdisciplinary study of relations among the quality of the physical environment, the health of the living environment, and human health. The interactions among these three spheres are driven by human activities, ecological processes, and natural earth processes; the interactions affect exposure to contaminants and pathogens and the severity of environmentally driven diseases in animals and people. This definition provides USGS with a framework for synthesizing natural science information from across the Bureau and providing it to environmental, natural resource, agricultural, and public health managers. USGS specializes in science at the environment-health interface, by characterizing the processes that affect the interaction among the physical environment, the living environment, and people, and the resulting factors that affect ecological and human exposure to disease agents. The USGS is a Federal science agency with a broad range of natural science expertise relevant to environmental health. USGS provides scientific information and tools as a scientific basis for management and policy decisionmaking. This report describes a 10-year strategy that encompasses the portfolio of USGS environmental health science. It summarizes national environmental health priorities that USGS is best suited to address, and will serve as a strategic framework for USGS environmental health science goals, actions, and outcomes for the next decade. Implementation of this strategy is intended to aid coordination of USGS environmental health activities and to provide a focal point for disseminating information to stakeholders. The “One Health” paradigm advocated by the World Health Organization (WHO; World Health Organization, 2011), and the American Veterinary Medical Association (AVMA; American Veterinary Medical Association, 2008), among others, is based on a general recognition that the health of humans, animals, and the environment are inextricably linked. Thus, successful efforts to protect that health will require increased interdisciplinary research and increased communication and collaboration among the broader scientific and health community. This strategy is built upon that paradigm.

Circular↗