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At least 1,225 records · Page 68Linked to original sources
USGS1988

Statistical summary of the chemical quality of surface water in the Powder River coal basin, the Hanna coal field, and the Green River coal region, Wyoming

A summary of the chemical quality of surface water in the three principal coal-producing areas of Wyoming was intensified by the U.S. Geologic Survey during 1975-81, in response to interest spurred by a dramatic increase in surface mining of the areas. This statistical summary consists of descriptive statistics and regression analyses of data from 72 stations on streams in the Powder River coal basin, the Hanna coal field, and the Green River coal region of Wyoming. The mean dissolved-solids concentrations in streams ranged from 15 to 4,800 mg/L. Samples collected near mountainous areas or in the upstream reaches of perennial streams in the plains had the smallest concentrations of dissolved solids, and the predominant ions were calcium and bicarbonate. Samples from ephemeral, intermittent, and the downstream reaches of perennial streams in the plains contained relatively large dissolved-solids concentrations, and the predominant ions usually were sodium and sulfate. Regression models showed that the concentrations of dissolved solids, calcium, magnesium, sodium, alkalinity, sulfate, and chloride correlated well with specific-conductance values in many of the streams. (USGS)

Water-Resources Investigations Report↗
USGS1996

Water quality, bed-sediment quality, and simulation of potential contaminant transport in Foster Creek, Berkeley County, South Carolina, 1991-93

Foster Creek, a freshwater tidal creek in Berkeley County, South Carolina, is located in an area of potential contaminant sources from residential, commercial, light industrial, and military activities. The creek is used as a secondary source of drinking water for the surrounding Charleston area. Foster Creek meets most of the freshwater- quality requirements of State and Federal regulatory agencies, but often contains low concentrations of dissolved oxygen and has been characterized as eutrophic. Investigations of water- and bed-sediment quality were made between 1991 and 1993 to assess the effects of anthropogenic sources of contamination on Foster Creek. Low-flow surface-water samples were generally free of toxic compounds with the exception of laboratory artifacts and naturally occurring trace metals. Storm-runoff samples generally contained very low concentrations (near detection limits) of a small number of volatile and semivolatile organics and naturally occurring trace metals. Concentrations of toxic compounds in excess of current (1995) South Carolina Department of Health and Environmental Control and U.S. Environmental Protection Agency regulations were not detected in surface-water samples collected from Foster Creek. Chemical analyses of streambed sediments indicated minimal anthropogenic effects on sediment quality. The particle-tracking option of the U.S. Geological Survey one-dimensional unsteady-flow model (BRANCH) indicated that as the simulated volume of rainfall runoff increased in the Foster Creek Basin, simulated particles in Foster Creek were transported greater distances. Simulating flow through the Bushy Park Dam (also known as Back River Dam) had little effect on particle movement in Foster Creek. Simulating typical withdrawal rates at a water-supply intake resulted in a slight attraction of particles toward the intake during conditions of relatively low runoff. These withdrawals had a greater influence on particles downstream of the intake than on those upstream of the intake. Simulations confirmed earlier findings which suggested that the creek would not flush during baseflow conditions, with the exception of the lower 1-mile reach, where flushing results from tidal movements. According to the simulations, Foster Creek will fully flush if a 2-year, 7-day storm occurs. Flushing appears to be affected more by the total volume of storm runoff than by typical municipal withdrawals or tidal effects.

South Carolina↗
USGS2019

Hydrologic balance, water quality, chemical-mass balance, and geochemical modeling of hyperalkaline ponds at Big Marsh, Chicago, Illinois, 2016–17

Hyperalkaline (pH greater than 12) ponds and groundwater exist at Big Marsh near Lake Calumet, Chicago, Illinois, a site used by the steel industry during the mid-1900s to deposit steel- and iron-making waste, in particular, slag. The hyperalkaline ponds may pose a hazard to human health and the environment. The U.S. Geological Survey (USGS), in cooperation with the Environmental Protection Agency (EPA) and in collaboration with the City of Chicago’s Park District, completed a study to evaluate the hydrologic balance, water quality, and chemical-mass balance of hyperalkaline ponds at Big Marsh and geochemical modeling used to evaluate remediation options for water quality at the site based on data collected in 2016–17. Synoptic measurements of surface-water and groundwater elevations were used to determine flow directions and to enable a preliminary estimate of the hydrologic balance for the ponds. Water-quality samples also were collected and analyzed for selected constituents including major anions and cations, nutrients, metals, and trace elements. The results of the water-quality analyses were used to develop a geochemical model to evaluate concentrations, factors affecting pH, and the state of equilibrium between surface waters and atmospheric carbon dioxide. The geochemical model was used to evaluate remediation scenarios using riprap, spillways, or active aeration. The results indicate that active aeration will decrease the pH to near 7.5 in about 8 hours, the fastest rate of the scenarios. Passive aeration, such as riprap or spillways, also can be effective at decreasing the pH in about 45 hours, but spatial obstacles limit their implementation. Seasonal variations in temperature also affect the rate of equilibration, where colder temperatures may have a lower pH than warmer temperatures and may affect the timing and frequency of remediation.

Illinois↗
USGS1994

U. S. Geological Survey Federal-State Cooperative Water-Resources Program Fiscal Year 1993

The Federal-State Cooperative Program is a part- nership between the U.S. Geological Survey and State and local agencies. It provides a balanced approach to the study and resolution of water- related problems and to acquiring hydrologic data. The principal program objectives are to: (1) collect, on a systematic basis, data needed for the continuing determination and evaluation of the quantity, quality, and use of the Nation's water resources, and (2) appraise the availa- bility and the physical, chemical, and biological characteristics of surface and ground water through analytical and interpretive investi- gations. During fiscal year 1993, hydrologic data collection, interpretive investigations, and research were conducted by Geological Survey personnel in offices in every State, Puerto Rico, and in several territories in cooperation with about 1,100 local, State, and regional agencies. In fiscal year 1993, Federal funding of $63.5 million was matched by cooperating agencies, which also provided almost $23 million unmatched for a total program of about $150 million. This amounted to nearly 40 percent of the total funds for Geological Survey water- resources activities. This report presents examples of current (1993) investigations. It also provides updated information on Cooperative Program investigations related to agricultural activities.

Open-File Report↗
USGS1979

Chemical composition of water and gas from five nearshore subaqueous springs in Clear Lake, Northern California

In 1971 The Geysers-Clear Lake area was selected by the U.S. Geological Survey geothermal research program as a region for extensive investigation. Under this program thermal water samples were first collected in December, 1974 during a winter of normal rainfall; the last samples were collected in February, 1977 during a period of drought. The drought exposed many springs which normally are submerged by Clear Lake. The collection and analysis of these springs is reported in Thompson and others (this vol.).

California↗
USGS1979

Hydrologic data for water-table aquifers in the greater Denver area, Front Range Urban Corridor, Colorado

As part of the U.S. Geological Survey 's investigations of the hydrology and geology in the Front Range Urban Corridor of Colorado, hydrologic data for water-table aquifers in the greater Denver area were collected and compiled during 1976-77. These data, consisting of records for 325 wells and 11 springs and chemical analyses of water for 272 of the wells and all 11 springs, are presented in tabular form. The tables contain data that were collected during the investigation, data compiled from reports published by the Colorado Water Conservation Board and the U.S. Geological Survey, and unpublished data from the files of the U.S. Geological Survey. State and local officials in the greater Denver area may find these data useful in planning for residential, commercial, and industrial development. (Woodard-USGS)

Open-File Report↗
USGS2009

Effects of simplifying fracture network representation on inert chemical migration in fracture-controlled aquifers

[1] While it is widely recognized that highly permeable ‘large‐scale' fractures dominate chemical migration in many fractured aquifers, recent studies suggest that the pervasive ‘small‐scale’ fracturing once considered of less significance can be equally important for characterizing the spatial extent and residence time associated with transport processes. A detailed examination of chemical migration through fracture‐controlled aquifers is used to advance this conceptual understanding. The influence of fracture structure is evaluated by quantifying the effects to transport caused by a systematic removal of fractures from three‐dimensional discrete fracture models whose attributes are derived from geologic and hydrologic conditions at multiple field sites. Results indicate that the effects to transport caused by network simplification are sensitive to the fracture network characteristics, degree of network simplification, and plume travel distance, but primarily in an indirect sense since correlation to individual attributes is limited. Transport processes can be ‘enhanced’ or ‘restricted’ from network simplification meaning that the elimination of fractures may increase or decrease mass migration, mean travel time, dispersion, and tailing of the concentration plume. The results demonstrate why, for instance, chemical migration may not follow the classic advection‐dispersion equation where dispersion approximates the effect of the ignored geologic structure as a strictly additive process to the mean flow. The analyses further reveal that the prediction error caused by fracture network simplification is reduced by at least 50% using the median estimate from an ensemble of simplified fracture network models, and that the error from network simplification is at least 70% less than the stochastic variability from multiple realizations.

Water Resources Research↗
USGS1967

Reconnaissance of the chemical quality of surface waters of the Neches River basin, Texas

The kinds and quantities of minerals dissolved in the surface water of the Neches River basin result from such environmental factors as geology, streamflow patterns and characteristics, and industrial influences. As a result of high rainfall in the basin, much of the readily soluble material has been leached from the surface rocks and soils. Consequently, the water in the streams is usually low in concentrations of dissolved minerals and meets the U.S. Public Health Service drinking-water standards. In most streams the concentration of dissolved solids is less than 250 ppm (parts per million). The Neches River drains an area of about 10,000 square miles in eastern Texas. From its source in southeast Van Zandt County the river flows in a general southeasterly direction and empties into Sabine Lake, an arm of the Gulf of Mexico. In the basin the climate ranges from moist subhumid to humid, and the average annual rainfall ranges from 46 inches is the northwest to more than 52 inches in the southeast. Annual runoff from the basin has averaged 11 inches; however, runoff rates vary widely from year to year. The yearly mean discharge of the Neches River at Evadale has ranged from 994 to 12,720 cubic feet per second. The rocks exposed in the Neches River basin are of the Quaternary and Tertiary Systems and range in age from Eocene to Recent. Throughout most of the basin the geologic formations dip generally south and southeast toward the gulf coast. The rate of dip is greater than that of the land surface; and as a result, the older formations crop out to the north of the younger formations. Water from the outcrop areas of the Wilcox Group and from the older formations of the Claiborne Group generally has dissolved-solids concentrations ranging from 100 to 250 ppm; water from the younger formations has concentrations less than 100 ppm. The northern half of the basin has soft water, with less than 60 ppm hardness. The southern half of .the basin has very soft water, usually with less than 30 ppm hardness. The chloride concentrations are less than 20 ppm in surface water in the southern half of the basin and usually range from 20 to 100 ppm in the northern half of the basin. Concentrations greater than 100 ppm are found only where pollution is occurring. The Neches River basin has an abundance of surface water, but uneven distribution of runoff makes storage projects necessary to provide dependable water supplies. The principal existing reservoirs, with the exception of Striker Creek Reservoir, contain water of excellent quality. Chemical-quality data for the Striker Creek drainage area indicate that its streams are affected by .the disposal of brines associated with oil production. Sam Rayburn Reservoir began impounding water in 1965. The water impounded should prove of acceptable quality for most uses, but municipal and industrial wastes released into the Angelina River near Lufkin may have a degrading effect on the quality of the water, especially during extended periods of low flows. Water available for storage at the many potential reservoir sites will be of good quality; but, if the proposed salt-water barrier is to impound acceptable water, the disposal of oilfield brine into Pine Island Bayou should be discontinued.

Water Supply Paper↗
USGS1982

Chemical and isotopic diversity in basalts dredged from the East Pacific Rise at 10°S, the fossil Galapagos Rise and the Nazca plate

We present petrographic, chemical and isotopic data for fresh lava samples dredged from three regions: (1) the fossil Galapagos Rise; (2) an elongate volcano near this extinct spreading center; and (3) the East Pacific Rise at 10°S. The samples from the Galapagos Rise are among the first samples from any fossil spreading center to be analyzed. Alkalic picrites from the elongate seamount and transitional basalts from the East Pacific Rise are both somewhat unusual rock types considering their respective tectonic environments. The dredges from the East Pacific Rise at about 10°S recovered unusual transitional, light rare-earth element (LREE) enriched basalts which show a range of fractionation. On the basis of their chemical and isotopic abundances, it is unlikely that the lavas are related by a single simple process of magmatic differentiation. We suggest that the mantle source region of these basalts was chemically and isotopically heterogeneous. The chemistry of LREE-depleted tholeiitic basalt dredged from near the axis of the extinct Galapagos Rise indicates complex petrogenesis and differentiation. The presence of tholeiitic basalts here indicates that unlike the Guadalupe and Mathematician fossil ridges, the Galapagos Rise has not been the site of voluminous post-abandonment alkalic volcanism. Alkalic basalts of picritic bulk composition dredged from an elongate seamount near the Galapagos Rise do not represent liquid compositions. Instead, we suggest that these alkalic liquids contain added olivine and plagioclase xenocrysts. Although most of the samples analyzed are very fresh, a few have been altered. The latter exhibit characteristic chemical and isotopic effects of seawater alteration.

Marine Geology↗
USGS1977

Long-term adequacy of metal resources

Although the earth's crust contains vast quantities of metals, extraction technologies and associated costs are inextricably bound to three fundamental geological factors — the amount of metal available in the earth's crust in each range of grades, the mineralogical form and chemical state of the metal, and the spatial distribution of the metal. The energy required to recover a given amount of metal increases substantially as grade declines. Most metal is produced from sulphide or oxide minerals, whereas most metal in the crust may be locked in the structures of the more refractory silicates. Recovery from silicate minerals could require orders of magnitude more energy than that used at present as also could exploitation of small, widely scattered or thin, deeply buried deposits. Although specific information on the fundamental factors is not available, each factor must in turn tend to further restrict exploitation. Independence of average grade and tonnage for many deposit types further reduces the availability of rock as a source of metal. In the long term, effects of these factors will be large increases in price for many metals.

Resources Policy↗
USGS2003

Atmospheric deposition maps for the Rocky Mountains

Variability in atmospheric deposition across the Rocky Mountains is influenced by elevation, slope, aspect, and precipitation amount and by regional and local sources of air pollution. To improve estimates of deposition in mountainous regions, maps of average annual atmospheric deposition loadings of nitrate, sulfate, and acidity were developed for the Rocky Mountains by using spatial statistics. A parameter-elevation regressions on independent slopes model (PRISM) was incorporated to account for variations in precipitation amount over mountainous regions. Chemical data were obtained from the National Atmospheric Deposition Program/National Trends Network and from annual snowpack surveys conducted by the US Geological Survey and National Park Service, in cooperation with other Federal, State and local agencies. Surface concentration maps were created by ordinary kriging in a geographic information system, using a local trend and mathematical model to estimate the spatial variance. Atmospheric-deposition maps were constructed at 1-km resolution by multiplying surface concentrations from the kriged grid and estimates of precipitation amount from the PRISM model. Maps indicate an increasing spatial trend in concentration and deposition of the modeled constituents, particularly nitrate and sulfate, from north to south throughout the Rocky Mountains and identify hot-spots of atmospheric deposition that result from combined local and regional sources of air pollution. Highest nitrate (2.5-3.0kg/ha N) and sulfate (10.0-12.0kg/ha SO4) deposition is found in northern Colorado.

Atmospheric Environment↗
USGS1958

Minerals of the cassiterite-bearing veins at Irish Creek, Virginia, and their paragenetic relations

Major rock types of the Irish Creek district are gneisses and schists, intruded by granodiorite. All these rocks are believed to be Precambrian. The ore deposits are fissure veins consisting largely of quartz veins bordered by greisen, and enriched by recurrent deposition. From field and microscopic evidence six stages of mineral formation have been deduced: 1. Crystallization of the granodiorite with the formation of hypersthene, augite, hornblende, andesine, orthoclase, microcline, and quartz; and accessory apatite, rutile, ilmenite, titanomagnetite, and zircon. 2. Metamorphism of the granodiorite and gneiss with formation of uralitic actinolite, epidote, and sphene. 3. A period of fracturing and formation of quartz veins. 4. Greisenization of the host rock producing first: coarse muscovite, brown biotite, cassiterite, beryl, wolframite, and quartz; then producing a second group of minerals-fluorite, green biotite, chlorite, phenakite, siderite, ankerite, parisite, sphalerite, sulfides, including aikinite and galeno-bismutite, leucoxene, fine muscovite, and quartz. 5. Formation of late vein minerals, clinozoisite, calcite, nontronite, and montmorillonite. 6. Formation of surficial alteration products, kaolinite, vermiculite, hematite, limonite, and scorodite. The italicized mineral names indicate the minerals heretofore unreported from Irish Creek; parisite, aikinite, and galenobismutite are new minerals for Virginia. Included in the detailed descriptions of all the minerals is a chemical analysis of beryl.

Virginia↗
USGS1945

Chemical analyses of surface waters in Oklahoma, September - December, 1944

A preliminary survey of the industrial quality of surface waters in Oklahoma was started in August, 1944, by the U.S. Geological Survey in cooperation with the Oklahoma Resources and Planning Board, with the Oklahoma A. & M. College, Engineering Experiment Station and Department of Chemistry. From September to December, 1944, three hundred and fifteen samples were obtained at eighty-four points where gages are maintained for measurement of discharge. Daily samples were collected at six stations, namely: Illinois River near Gore, Oklahoma Cimarron River near Oilton, Oklahoma Canadian River near Whitefield, Oklahoma Washita River near Durwood, Oklahoma Red River near Gainesville, Texas Red River at Denison Dam, Texas Sport samples were collected at the remainder of the stations. The analyses of the spot samples were made largely in a laboratory provided by the Oklahoma A. & M. College, under the supervision of Dr. O.M. Smith, Head, Department of Chemistry; Dr. S.R. Wood, Associate Professor of Chemistry; and W.W. Hastings, U.S. Geological Survey. The daily samples were analyzed in the water resources laboratory of the Geological Survey at Austin, Texas. These data have been summarized in a report to the Oklahoma Planning and Resources Board prepared by the U.S. Geological Survey, March 1, 1945. The streams of Oklahoma are classified into two major drainage basins: the Arkansas River and the Red River and their tributaries. The attached analyses are arranged in geographical order for their respective drainage basins, with records listed in downstream order for stations on the main stem first, followed by the analyses for the tributaries. When available, the mean daily discharge is given for the analyses.

Oklahoma;Texas↗
USGS2007

Processes Affecting Phosphorus and Copper Concentrations and Their Relation to Algal Growth in Two Supply Reservoirs in the Lower Coastal Plain of Virginia, 2002-2003, and Implications for Alternative Management Strategies

Elevated phosphorus concentrations commonly promote excessive growth of algae in waters nationwide. When such waters are used for public supply, the algae can plug filters during treatment and impart tastes and odors to the finished water. This increases treatment costs and results in finished water that may not be of the quality desired for public supply. Consequently, copper sulfate is routinely applied to many reservoirs to control algal growth but only is a 'temporary fix' and must be reapplied at intervals that can range from more than 30 days in the winter to less than 7 days in the summer. Because copper has a maximum allowable concentration in public drinking water and can be toxic to aquatic life, water suppliers commonly seek to develop alternative, long-term strategies for managing reservoirs. Because these are nationwide issues and part of the mission of the U.S. Geological Survey (USGS) is to define and protect the quality of the Nation's water resources and better understand the physical, chemical, and biological processes in wetlands, lakes, reservoirs, and estuaries, investigations into these issues are important to the fulfillment of the mission of the USGS. The City of Newport News, Virginia, provides 50 million gallons per day of treated water for public supply from Lee Hall and Harwoods Mill Reservoirs (terminal reservoirs) to communities on the lower York-James Peninsula. About 3,500 pounds of copper sulfate are applied to each reservoir at 3- to 99-day intervals to control algal growth. Consequently, the USGS, in cooperation with the City of Newport News, investigated the effects of management practices and natural processes on phosphorus (the apparent growth-limiting nutrient), copper, and algal concentrations in the terminal reservoirs to provide information that can be used to develop alternative management strategies for the terminal reservoirs. Initial parts of the research evaluated circulation and stratification in the reservoirs because these factors affect phosphorus availability to algae. Results indicate that (1) water flows through both reservoirs in a 'plug-flow' manner; (2) little water in the lower part of Lee Hall Reservoir, into which pumped water enters, flows into the upper part of the reservoir and mixes with that water; (3) Lee Hall Reservoir generally does not stratify; and (4) Harwoods Mill Reservoir stratifies from April to June through September or October into an upper epilimnion that does not mix with water in the lower hypolimnion. The ratio of dissolved nitrogen to phosphorus concentrations (N:P) for sites in both reservoirs generally was greater than 20:1, indicating that phosphorus likely is the growth-limiting nutrient in both reservoirs. Phosphorus was present predominantly as suspended, rather than dissolved, species except in the hypolimnion of Harwoods Mill Reservoir and the natural inflow represented by Baptist Run. Because Harwoods Mill Reservoir stratified, field-measured physical and chemical characteristics and concentrations of nitrogen and phosphorus species changed sharply over short depth intervals in this reservoir. Dissolved phosphorus concentration increased from 0.015 to 0.057 milligrams per liter between a depth of 15 feet (ft) and the bottom (depth of 18 ft), indicating the release of phosphorus by the decomposition of organic material and(or) the reduction of iron oxides in bed sediment and the lower water column. Because the mixing boundary between the epilimnion and the hypolimnion likely was between depths of 6 and 10 ft, such sources in the hypolimnion would not contribute phosphorus to the growth of algae in the epilimnion from which water is withdrawn for supply until the breakdown of stratification in the fall. Furthermore, laboratory studies of samples from both reservoirs indicated that dissolved phosphorus was released from suspended particles at rates of 0.0007 to 0.0019 milligrams per liter per day. At these rates of release, particl

Scientific Investigations Report↗
USGS2015

Hydrogeologic framework, hydrology, and refined conceptual model of groundwater flow for Coastal Plain aquifers at the Standard Chlorine of Delaware, Inc. Superfund Site, New Castle County, Delaware, 2005-12

From 1966 to 2002, activities at the Standard Chlorine of Delaware chemical facility in New Castle County, Delaware resulted in the contamination of groundwater, soils, and wetland sediment. In 2005, the U.S. Geological Survey (USGS), in partnership with the U.S. Environmental Protection Agency, Region 3, and the Delaware Department of Natural Resources and Environmental Control began a multi-year investigation of the hydrogeologic framework and hydrology of the confined aquifer system. The goals of the ongoing study at the site (the Potomac Aquifer Study) are to determine the hydraulic connection between the Columbia and Potomac aquifers, determine the direction of groundwater flow in the Potomac aquifer, and identify factors affecting the fate of contaminated groundwater. This report describes progress made towards these goals based on available data collected through September 2012. The regional hydrogeologic framework indicates that the site is underlain by Coastal Plain sediments of the Columbia, Merchantville, and Potomac Formations. Two primary aquifers underlying the site, the Columbia and the upper Potomac, are separated by the Merchantville Formation confining unit. Local groundwater flow in the surficial (Columbia) aquifer is controlled by topography and generally flows northward and discharges to nearby surface water. Regional flow within the Potomac aquifer is towards the southeast, and is strongly influenced by major water withdrawals locally. Previous investigations at the site indicated that contaminants, primarily benzene and chlorinated benzene compounds, were present in the Columbia aquifer in most locations; however, there were only limited detections in the upper Potomac aquifer as of 2004. From 2005 through 2012, the USGS designed a monitoring network, assisted with exploratory drilling, collected data at monitoring wells, conducted geophysical surveys, evaluated water-level responses in wells during pumping of a production well, and evaluated major aquifer withdrawals. Data collected through these efforts were used to refine the local conceptual flow system. The refined conceptual flow system for the site includes: (a) identification of gaps in confining units in the study area, (b) identification and correlation of multiple water-bearing sand intervals within the upper Potomac Formation, (c) connections between groundwater and surface water, (d) connections between shallow and deeper groundwater, (e) new water-level (or potentiometric surface) maps and inferred flow directions, and (f) identification of major local pumping well influences. The implications of the revised conceptual flow system on the occurrence and movement of site contaminants are that the resulting detection of contaminants in the upper Potomac aquifer at specific well locations can be attributed primarily to either advective lateral transport, direct vertical contaminant transport, or a combination of vertical and lateral movement resulting from changes in water withdrawal rates over time.

Delaware↗
USGS2006

Chapter A6. Section 6.1. Temperature

Accurate temperature measurements are required for accurate determinations of important environmental parameters such as pH, specific electrical conductance, and dissolved oxygen, and to the determination of chemical reaction rates and equilibria, biological activity, and physical fluid properties. This section of the National Field Manual (NFM) describes U.S. Geological Survey (USGS) guidance and protocols for measurement of temperature in air, ground water, and surface water and calibration of the equipment used. Each chapter of the National Field Manual is published separately and revised periodically. Newly published and revised chapters will be announced on the USGS Home Page on the World Wide Web under 'New Publications of the U.S. Geological Survey.'

Techniques of Water-Resources Investigations↗
USGS1982

Water resources data, West Virginia water year 1981, Appendix - coal areas and special projects

The first section of this report contains data collected during the 1981 water year for the West Virginia Coal Hydrology monitoring project. Records consist of discharge and water-quality data collected at 246 sites in July, at 29 sites in August, and sediment data for 235 sites collected in July. The second section of this report contains data collected during the period January 1978 to December 1981 for the water resources study of the Tug Fork and Twelvepole Creek basins. Records consist of physical data for 347 wells, water level data for two wells, quality analyses of water from 328 wells, and discharge, chemical and biological data for 91 sites sampled several times.

West Virginia↗
USGS1998

Guidelines for quality assurance and quality control of fish taxonomic data collected as part of the National Water-Quality Assessment Program

Fish community structure is characterized by the U.S. Geological Survey's National Water-Quality Assessment (NAWQA) Program as part of a perennial, multidisciplinary approach to evaluating the physical, chemical, and biological conditions of the Nation's water resources. The objective of quality assurance and quality control of fish taxonomic data that are collected as part of the NAWQA Program is to establish uniform guidelines and protocols for the identification, processing, and archiving of fish specimens to ensure that accurate and reliable data are collected. Study unit biologists, collaborating with regional biologists and fish taxonomic specialists, prepare a pre-sampling study plan that includes a preliminary faunal list and identification of an ichthyological curation center for receiving preserved fish specimens. Problematic taxonomic issues and protected taxa also are identified in the study plan, and collecting permits are obtained in advance of sampling activities. Taxonomic specialists are selected to identify fish specimens in the field and to assist in determining what fish specimens should be sacrificed, fixed, and preserved for laboratory identification, independent taxonomic verification, and long-term storage in reference or voucher collections. Quantitative and qualitative sampling of fishes follows standard methods previously established for the NAWQA Program. Common ichthyological techniques are used to process samples in the field and prepare fish specimens to be returned to the laboratory or sent to an institutional repository. Taxonomic identifications are reported by using a standardized list of scientific names that provides nomenclatural consistency and uniformity across study units.

Water-Resources Investigations Report↗