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USGS2011

Physical and chemical characteristics including total and geochemical forms of phosphorus in sediment from the top 30 centimeters of cores collected in October 2006 at 26 sites in Upper Klamath Lake, Oregon

μThis study of phosphorus (P) cycling in eutrophic Upper Klamath Lake (UKL), Oregon, was conducted by the U.S. Geological Survey in cooperation with the U.S. Bureau of Reclamation. Lakebed sediments from the upper 30 centimeters (cm) of cores collected from 26 sites were characterized. Cores were sampled at 0.5, 1.5, 2.5, 3.5, 4.5, 10, 15, 20, 25, and 30 cm. Prior to freezing, water content and sediment pH were determined. After being freeze-dried, all samples were separated into greater than 63-micron (μm) particle-size (coarse) and less than 63-μm particle-size (fine) fractions. In the surface samples (0.5 to 4.5 cm below the sediment water interface), approximately three-fourths of the particles were larger than 63-μm. The ratios of the coarse particle-size fraction (>63 μm) and the fine particle-size fraction (<63 μm) were approximately equal in samples at depths greater than 10 cm below the sediment water interface. Chemical analyses included both size fractions of freeze-dried samples. Chemical analyses included determination of total concentrations of aluminum (Al), calcium (Ca), carbon (C), iron (Fe), poorly crystalline Fe, nitrogen (N), P, and titanium (Ti). Total Fe concentrations were the largest in sediment from the northern portion of UKL, Howard Bay, and the southern portion of the lake. Concentrations of total Al, Ca, and Ti were largest in sediment from the northern, central, and southernmost portions of the lake and in sediment from Howard Bay. Concentrations of total C and N were largest in sediment from the embayments and in sediment from the northern arm and southern portion of the lake in the general region of Buck Island. Concentrations of total C were larger in the greater than 63-μm particle-size fraction than in the less than 63-μm particle-size fraction. Sediments were sequentially extracted to determine concentrations of inorganic forms of P, including loosely sorbed P, P associated with poorly crystalline Fe oxides, and P associated with mineral phases. The difference between the concentration of total P and sum of the concentrations of inorganic forms of P is referred to as residual P. Residual P was the largest fraction of P in all of the sediment samples. In UKL, the correlation between concentrations of total P and total Fe in sediment is poor (R2<0.1). The correlation between the concentrations of total P and P associated with poorly crystalline Fe oxides is good (R2=0.43) in surface sediment (0.5-4.5 cm below the sediment water interface) but poor (R2<0.1) in sediments at depths between 10 cm and 30 cm. Phosphorus associated with poorly crystalline Fe oxides is considered bioavailable because it is released when sediment conditions change from oxidizing to reducing, which causes dissolution of Fe oxides.

Oregon↗

USGS2009

Regional variations in water quality and relationships to soil and bedrock weathering in the southern Sacramento Valley, California, USA

Regional patterns in ground- and surface-water chemistry of the southern Sacramento Valley in California were evaluated using publicly available geochemical data from the US Geological Survey's National Water Information System (NWIS). Within the boundaries of the study area, more than 2300 ground-water analyses and more than 20,000 surface-water analyses were available. Ground-waters from the west side of the Sacramento Valley contain greater concentrations of Na, Ca, Mg, B, Cl and SO 4 , while the east-side ground-waters contain greater concentrations of silica and K. These differences result from variations in surface-water chemistry as well as from chemical reactions between water and aquifer materials. Sediments that fill the Sacramento Valley were derived from highlands to the west (the Coast Ranges) and east (the Sierra Nevada Mountains), the former having an oceanic provenance and the latter continental. These geologic differences are at least in part responsible for the observed patterns in ground-water chemistry. Thermal springs that are common along the west side of the Sacramento Valley appear to have an effect on surface-water chemistry, which in turn may affect the ground-water chemistry.

Applied Geochemistry↗

USGS2008

Alkylphenols, other endocrine-active chemicals, and fish responses in three streams in Minnesota — Study design and data, February-September 2007

This report presents the study design and environmental data for an integrated chemical and biological study of three streams (South Fork Crow River, Redwood River, and Grindstone River) that receive wastewater in Minnesota. The objective of the study was to identify distribution patterns of endocrine-active chemicals and other organic chemicals indicative of wastewater, and to identify fish responses in the same streams. Endocrine-active chemicals are a class of chemicals that interfere with the natural regulation of endocrine systems, and an understanding of their distribution in aquatic systems is important so that aquatic organism exposure can be evaluated. This study was a cooperative effort of the U.S. Geological Survey (USGS), the Minnesota Pollution Control Agency, and St. Cloud State University (St. Cloud, Minn.). The USGS collected and analyzed water and quality-assurance samples and measured streamflow during six sampling events in each of three streams. Water samples were collected upstream from and at two successive points downstream from wastewater-treatment plant (WWTP) effluent discharge and from treated effluent from February through September 2007. Bed-sediment samples were collected during one sampling period at each of the stream locations. Water and bed-sediment samples were analyzed for endocrine-active chemicals including alkylphenols, alkylphenol polyethoxylates, and nonylphenol ethoxycarboxlylates (NPECs). Water samples also were analyzed for major ions, nutrients, and organic carbon. In addition, as part of an intensive time-series investigation, the USGS staff collected daily water samples for 8 weeks from the Redwood River near Marshall, Minn., for analyses of total alkylphenols and atrazine. St. Cloud State University staff collected and analyzed fish to determine male fish responses at all water sampling sites and at an additional site near the discharge of wastewater-treatment plant effluent to these streams. Male fish responses included the presence and concentration of vitellogenin in plasma, gonadosomatic indices, and histological characterizations of liver and testes tissue. Hydrologic, chemical and biological characteristics were different among sites. The percentage of streamflow contributed by WWTP effluent (ranging from less than 1 to 79 percent) was greatest at the South Fork Crow River and least at the Grindstone River. WWTP effluent generally contributed the greatest percentage of streamflow during winter and late summer when streamflows were low. A wide variety of chemicals were detected. More chemicals were detected in WWTP effluent samples than in stream samples during most time periods. The most commonly detected chemicals in samples collected monthly and analyzed at the USGS National Research Program Laboratory were 2,6-di- tert -butyl-1,4-benzoquinone, 2,6-di- tert -butyl-4-methylphenol, 3- beta -coprostanol, 4-methylphenol, 4-nonylphenol (NP), 4- tert -octylphenol, bisphenol A, cholesterol, ethylenediaminetetraacetic acid, and triclosan. The chemicals 4-nonylphenolmonoethoxycarboxylate (NP1EC), 4-nonylphenoldiethoxycarboxylate (NP2EC), and 4-nonylphenoltriethoxycarboxylate (NP3EC) also were detected. Excluding nondetections, the sum of NP1EC through NP3EC concentrations ranged from 5.1 to 260 µg/L among all samples. NP was detected in upstream, effluent, and downstream samples in each stream during at least one time period. NP was detected in 49 percent of environmental samples. Excluding nondetections, concentrations of NP ranged from 100 to 880 nanograms per liter among all samples. NP was also detected in more than one-half of the bed-sediment samples. The most commonly detected wastewater indicator chemicals in samples analyzed by schedule 4433 at the USGS National Water Quality Laboratory were 3,4-dichlorophenyl isocyanate, acetyl-hexamethyl-tetrahydronaphthalene, benzophenone, cholesterol, hexahydrohexamethyl-cyclopenta-benzopyran, N,N-diethyl- meta -toluamide, and tri(dichloroisopropyl) phosphate. Male fish responses were the focus of the fish analyses, and 508 male fish were collected among all sampling sites. Vitellogenin was detected in 57 percent of the 415 male fish analyzed; concentrations ranged from an estimated value of 0.1 to 330 micrograms per milliliter (µg/mL) (average of 17.1 µg/mL). Intersex (the presence of oocytes in testes tissue) was observed in only one fathead minnow from an upstream site on the Grindstone River.

Minnesota↗

USGS2017

Optimal hydrograph separation using a recursive digital filter constrained by chemical mass balance, with application to selected Chesapeake Bay watersheds

Quantitative estimates of base flow are necessary to address questions concerning the vulnerability and response of the Nation’s water supply to natural and human-induced change in environmental conditions. An objective of the U.S. Geological Survey National Water-Quality Assessment Project is to determine how hydrologic systems are affected by watershed characteristics, including land use, land cover, water use, climate, and natural characteristics (geology, soil type, and topography). An important component of any hydrologic system is base flow, generally described as the part of streamflow that is sustained between precipitation events, fed to stream channels by delayed (usually subsurface) pathways, and more specifically as the volumetric discharge of water, estimated at a measurement site or gage at the watershed scale, which represents groundwater that discharges directly or indirectly to stream reaches and is then routed to the measurement point. Hydrograph separation using a recursive digital filter was applied to 225 sites in the Chesapeake Bay watershed. The recursive digital filter was chosen for the following reasons: it is based in part on the assumption that groundwater acts as a linear reservoir, and so has a physical basis; it has only two adjustable parameters (alpha, obtained directly from recession analysis, and beta, the maximum value of the base-flow index that can be modeled by the filter), which can be determined objectively and with the same physical basis of groundwater reservoir linearity, or that can be optimized by applying a chemical-mass-balance constraint. Base-flow estimates from the recursive digital filter were compared with those from five other hydrograph-separation methods with respect to two metrics: the long-term average fraction of streamflow that is base flow, or base-flow index, and the fraction of days where streamflow is entirely base flow. There was generally good correlation between the methods, with some biased slightly high and some biased slightly low compared to the recursive digital filter. There were notable differences between the days at base flow estimated by the different methods, with the recursive digital filter having a smaller range of values. This was attributed to how the different methods determine cessation of quickflow (the part of streamflow which is not base flow). For 109 Chesapeake Bay watershed sites with available specific conductance data, the parameters of the filter were optimized using a chemical-mass-balance constraint and two different models for the time-dependence of base-flow specific conductance. Sixty-seven models were deemed acceptable and the results compared well with non-optimized results. There are a number of limitations to the optimal hydrograph-separation approach resulting from the assumptions implicit in the conceptual model, the mathematical model, and the approach taken to impose chemical mass balance (including tracer choice). These limitations may be evidenced by poor model results; conversely, poor model fit may provide an indication that two-component separation does not adequately describe the hydrologic system’s runoff response. The results of this study may be used to address a number of questions regarding the role of groundwater in understanding past changes in stream-water quality and forecasting possible future changes, such as the timing and magnitude of land-use and management practice effects on stream and groundwater quality. Ongoing and future modeling efforts may benefit from the estimates of base flow as calibration targets or as a means to filter chemical data to model base-flow loads and trends. Ultimately, base-flow estimation might provide the basis for future work aimed at improving the ability to quantify groundwater discharge, not only at the scale of a gaged watershed, but at the scale of individual reaches as well.

Scientific Investigations Report↗

USGS1978

Historical profile, Quality of Water Laboratories, U. S. Geological Survey

During the period 1918 to 1973 the U.S. Geological Survey, Water Resources Division, established 22 District-type water quality laboratories. These facilities provided the analytical capability and water-quality information for hydrologic investigations and the national baseline inventory of chemical, physical, fluvial sediment, and biological characteristics of surface and ground waters in the United States. Prior to 1950, most methods used in the laboratory were gravimetric, colorimetric, or titrimetric. Flame photometric equipment was common to most laboratories in the 1950's, and the atomic absorption spectrophotometer was added to larger laboratories in the 1960's. In the late 1960's, the first of the automatic analyzers was installed. Total annual production averaged about 480 adjusted complete analyses during the early years 1919-28, about 7,800 in 1946, and about 50,000 in 1970. Budget estimates for the majority of laboratories ranged from $25,000 to $50,000 (1940-50) and $75,000 to $300,000 (1965-73). Beginning in 1972, major functions of the 22 laboratories have been combined into two comprehensive highly-automated facilities located at Denver (Arvada), Colo., and Atlanta (Doraville), Ga. These laboratories comprise the Central Laboratory System for the U.S. Geological Survey. (Woodard-USGS)

Open-File Report↗

USGS2012

Geologic evidence for a magma chamber beneath Newberry Volcano, Oregon

At Newberry Volcano, central Oregon, more than 0.5 m.y. of magmatic activity, including caldera collapse and renewed caldera-filling volcanism, has created a structural and thermal chimney that channels magma ascent. Holocene rhyolitic eruptions (1) have been confined mainly within the caldera in an area 5 km in diameter, (2) have been very similar in chemical composition, phenocryst mineralogy, and eruptive style, and (3) have occurred as recently as 1300 years ago, with repose periods of 2000–3000 years between eruptions. Holocene basaltic andesite eruptions are widespread on the flanks but are excluded from the area of rhyolitic volcanism. Basaltic andesite in fissures at the edge of the rhyolite area has silicic inclusions and shows mixed basalt-rhyolite magma relations. These geologic relations and the high geothermal gradient that characterizes the lower part of a drill hole in the caldera (U.S. Geological Survey Newberry 2) indicate that a rhyolitic magma chamber has existed beneath the caldera throughout the Holocene. Its longevity probably is a result of intermittent underplating by basaltic magma.

Journal of Geophysical Research Solid Earth↗

USGS2006

Application of municipal biosolids to dry-land wheat fields - A monitoring program near Deer Trail, Colorado (USA). A presentation for an international conference: "The Future of Agriculture: Science, Stewardship, and Sustainability", August 7-9, 2006, Sacramento, CA

Since late 1993, Metro Wastewater Reclamation District of Denver (Metro District), a large wastewater treatment plant in Denver, Colorado, has applied Grade I, Class B biosolids to about 52,000 acres of non-irrigated farmland and rangeland near Deer Trail, Colorado. In cooperation with the Metro District in 1993, the U.S. Geological Survey (USGS) began monitoring ground water at part of this site. In 1999, the USGS began a more comprehensive study of the entire site to address stakeholder concerns about the chemical effects of biosolids applications. This more comprehensive monitoring program has recently been extended through 2010. Monitoring components of the more comprehensive study included biosolids collected at the wastewater treatment plant, soil, crops, dust, alluvial and bedrock ground water, and stream bed sediment. Streams at the site are dry most of the year, so samples of stream bed sediment deposited after rain were used to indicate surface-water effects. This presentation will only address biosolids, soil, and crops. More information about these and the other monitoring components are presented in the literature (e.g., Yager and others, 2004a, b, c, d) and at the USGS Web site for the Deer Trail area studies at http://co.water.usgs.gov/projects/CO406/CO406.html. Priority parameters identified by the stakeholders for all monitoring components, included the total concentrations of nine trace elements (arsenic, cadmium, copper, lead, mercury, molybdenum, nickel, selenium, and zinc), plutonium isotopes, and gross alpha and beta activity, regulated by Colorado for biosolids to be used as an agricultural soil amendment. Nitrogen and chromium also were priority parameters for ground water and sediment components. In general, the objective of each component of the study was to determine whether concentrations of priority parameters (1) were higher than regulatory limits, (2) were increasing with time, or (3) were significantly higher in biosolids-applied areas than in a similar farmed area where biosolids were not applied. Where sufficient samples could be collected, statistical methods were used to evaluate effects. Rigorous quality assurance was included in all aspects of the study. The roles of hydrology and geology also were considered in the design, data collection, and interpretation phases of the study. Study results indicate that the chemistry of the biosolids from the Denver plant was consistent during 1999-2005, and total concentrations of regulated trace elements were consistently lower than the regulatory limits. Plutonium isotopes were not detected in the biosolids. Leach tests using deionized water to simulate natural precipitation indicate arsenic, molybdenum, and nickel were the most soluble priority parameters in the biosolids. Study results show no significant difference in concentrations of priority parameters between biosolids-applied soils and unamended soils where no biosolids were applied. However, biosolids were applied only twice during 1999-2003. The next soil sampling is not scheduled until 2010. To date concentrations of most of the priority parameters were not much greater in the biosolids than in natural soil from the sites. Therefore, many more biosolids applications would need to occur before biosolids effects on the soil priority constituents can be quantified. Leach tests using deionized water to simulate precipitation indicate that molybdenum and selenium were the priority parameters that were most soluble in both biosolids-applied soil and natural or unamended soil. Study results do not indicate significant differences in concentrations of priority parameters between crops grown in biosolids-applied areas and crops grown where no biosolids were applied. However, crops were grown only twice during 1999-2003, so only two crop samples could be collected. The wheat-grain elemental data collected during 1999-2003 for both biosolids-applied areas and unamended areas are similar

Open-File Report↗

USGS1971

Microearthquake activity in the vicinity of Wooded Island, Hanford region, Washington

The U.S. Geological Survey (U.S.G.S.) began to monitor microearthquake activity in the region of the Atomic Energy Commission's Hanford Reservation in south-central Washington in March 1969. The Division of Reactor Development and Technology (DRDT), of the Atomic Energy Commission (AEC), supported the operation of a network of 6 (later 7) short-period, high-gain seismograph stations (Figure 1) through June 1970. Then the Chemical Processing Division (CPD) of the AEC assumed support of the original 7-station network and added 9 additional stations (Figure 1). Some preliminary results from the 7-station network covering the period 23 March 1969 to 31 December 1969 were released in the U.S.G.S. open-file4report "Geologic Investigation of Faulting in the Hanford Region, Washington", by James W. Bingham, Clark J. Landquist, and Elmer H. Baltz. Preliminary reports on the results from the seismograph network for 1970 have been submitted to the AEC. This report covers a specific zone of microearthquake activity located near Wooded Island in the Columbia River, which flows along the east side of the Hanford Reservation (Figure 1). The data cover the period 23 March 1969 to 28 February 1971.

Washington↗

USGS2015

Hydrologic data for the Walker River Basin, Nevada and California, water years 2010–14

Walker Lake is a threatened and federally protected desert terminal lake in western Nevada. To help protect the desert terminal lake and the surrounding watershed, the Bureau of Reclamation and U.S. Geological Survey have been studying the hydrology of the Walker River Basin in Nevada and California since 2004. Hydrologic data collected for this study during water years 2010 through 2014 included groundwater levels, surface-water discharge, water chemistry, and meteorological data. Groundwater levels were measured in wells, and surface-water discharge was measured in streams, canals, and ditches. Water samples for chemical analyses were collected from wells, streams, springs, and Walker Lake. Chemical analyses included determining physical properties; the concentrations of major ions, nutrients, trace metals, dissolved gases, and radionuclides; and ratios of the stable isotopes of hydrogen and oxygen. Walker Lake water properties and meteorological parameters were monitored from a floating platform on the lake. Data collection methods followed established U.S. Geological Survey guidelines, and all data are stored in the National Water Information System database. All of the data are presented in this report and accessible on the internet, except multiple-depth Walker Lake water-chemistry data, which are available only in this report.

California, Nevada↗

USGS1958

Determination of the oxidation state of uranium in apatite and phosphorite deposits

Geological and mineralogical evidence indicate that the uranium present in apatite may proxy for calcium in the mineral structure as U(IV). An experimental investigation was conducted and chemical evidence was obtained that establishes the presence of U(IV) in apatite. The following analytical procedure was developed for the determination of U(IV). Carbonatefluorapatite is dissolved in 1.5 M orthophosphoric acid at a temperature of 5°C or slightly below and fluorapatite is dissolved in cold 1.2 M hydrochloric acid (approximately 5°C) containing 1.5 g of hydroxylamine hydrochloride per 100 ml. Uranium(IV) is precipitated by cupferron using titanium as a carrier. The uranium in the precipitate is separated by use of the ethyl acetate extraction procedure and determined fluorimetrically. The validity and the limitations of the method have been established by spike experiments.

Geochimica et Cosmochimica Acta↗

USGS2021

Multiple in-stream stressors degrade biological assemblages in five U.S. regions

Biological assemblages in streams are affected by a wide variety of physical and chemical stressors associated with land-use development, yet the importance of combinations of different types of stressors is not well known. From 2013 to 2017, the U.S. Geological Survey completed multi-stressor/multi-assemblage stream ecological assessments in five regions of the United States (434 streams total). Diatom, invertebrate, and fish communities were enumerated, and five types of potential stressors were quantified: habitat disturbance, excess nutrients, high flows, basic water quality, and contaminants in water and sediment. Boosted regression tree (BRT) models for each biological assemblage and region generally included variables from all five stressor types and multiple stressors types in each model was the norm. Classification and regression tree (CART) models then were used to determine thresholds for each BRT model variable above which there appeared to be adverse effects (multi-metric index (MMI) models only). In every region and assemblage there was a significant inverse relation between the MMI and the number of stressors exerting potentially adverse effects. The number of elevated instream stressors often varied substantially for a given level of land-use development and the number of elevated stressors was a better predictor of biological condition than was development. Using the adverse effects-levels that were developed based on the BRT model results, 68% of the streams had two or more stressors with potentially adverse effects and 35% had four or more. Our results indicate that relatively small increases in the number of stressors of different types can have a large effect on a stream ecosystem.

Science of the Total Environment↗

USGS2000

Transport, behavior, and fate of volatile organic compounds in streams

Volatile organic compounds (VOCs) are compounds with chemical and physical properties that allow the compounds to move freely between the water and air phases of the environment. VOCs are widespread in the environment because of this mobility. Many VOCs have properties that make them suspected or known hazards to the health of humans and aquatic organisms. Consequently, understanding the processes affecting the concentration and distribution of VOCs in the environment is necessary. The transport, behavior, and fate of VOCs in streams are determined by combinations of chemical, physical, and biological processes. These processes are volatilization, absorption, wet and dry deposition, microbial degradation, sorption, hydrolysis, aquatic photolysis, oxidation, chemical reaction, biocon-centration, advection, and dispersion. The relative importance of each of these processes depends on the characteristics of the VOC and the stream. The U.S. Geological Survey National Water-Quality Assessment Program selected 55 VOCs for study. This article reviews the characteristics of the various processes that could affect the transport, behavior, and fate of these VOCs in streams.

Critical Reviews in Environmental Science and Tech↗

USGS1960

Deposits of the manganese oxides

One of the problems of the wartime program of studies of domestic manganese deposits concerned the identification of, and modes of origin of the manganese oxide minerals. Of the hundreds of specimens of the oxides collected in the United States, the minerals of about 250 specimens were identified by X-ray analysis; complete chemical analyses were made of about 35 specimens and partial analyses of about 150 specimens. This report presents the conclusions that arise out of a review of the geologic environment under which the specimens were found. One conclusion of this review concerns the supergene vs. hypogene origin of the oxides. In order to reach conclusions concerning the supergene and hypogene origin of the 33 oxides of manganese recognized thus far, it was necessary to define the criteria that seemed usable.One group of oxides appears to be persistently supergene: groutite, hydrohausmannite, lithiophorite, rancieite, hetaerolite, hydrohetaerolite, chalcophanite, crednerite, woodruffite, and wad. Another group of oxides appears to have been formed only by hypogene processes: manganosite, hausmannite, pyrochroite, bixbyite, galaxite, jacobsite, franklinite, pyrophanite, and ilmenite. A third group of oxides appear to have been formed by supergene processes in some places and by hypogene processes in other places: manganite, pyrolusite, ramsdellite, cryptomelane, psilomelane, hollandite, braunite, and coronadite.Another conclusion concerns a genetic relation between: (1) veins of manganese oxides in the southwest, largely in Tertiary volcanic rocks, (2) bodies of oxides in travertine aprons near active hot springs, and inactive Pleistocene springs, and (3) stratified oxides, largely in late Tertiary sedimentary rocks in the southwest. From the features of these three groups of deposits of oxides and their geologic and geographic distribution, it appears that hot water from great depth rose on fractures in areas of volcanic activity, deposited oxides in the fractures, appeared at the surface as hot springs, deposited oxides in the aprons near the springs and continuing to local basins, deposited manganese oxides with local debris as persistent beds in sediments, partly or wholly of volcanic origin.

Economic Geology↗

USGS2006

Effects of urban development on stream ecosystems alongthe Front Range of the Rocky Mountains, Colorado and Wyoming

The U.S. Geological Survey (USGS) conducted a study from 2002 through 2003 through its National Water-Quality Assessment (NAWQA) Program to determine the effects of urbanization on the physical, chemical, and biological characteristics of stream ecosystems along the Front Range of the Rocky Mountains. The objectives of the study were to (1) examine physical, chemical, and biological responses at sites ranging from minimally to highly developed; (2) determine the major physical, chemical, and landscape variables affecting aquatic communities at these sites; and (3) evaluate the relevance of the results to the management of water resources in the South Platte River Basin.

Fact Sheet↗

USGS2000

Chemical data and lead isotopic compositions of geochemical baseline samples from streambed sediments and smelter slag, lead isotopic compositions in fluvial tailings, and dendrochronology results from the Boulder River watershed, Jefferson County, Montana

Introduction As a part of the U.S. Geological Survey Abandoned Mine Lands Initiative, metal-mining related wastes in the Boulder River study area in northern Jefferson County, Montana, have been evaluated for their environmental effects. The study area includes a 24-km segment of the Boulder River in and around Basin, Montana and three principal tributaries to the Boulder River: Basin Creek, Cataract Creek, and High Ore Creek. Mine and prospect waste dumps and mill wastes are located throughout the drainage basins of these tributaries and in the Boulder River. Mine-waste material has been transported into and down streams, where it has mixed with and become incorporated into the streambed sediments. In some localities, mine waste material was placed directly in stream channels and was transported downstream forming fluvial tailings deposits along the stream banks. Water quality and aquatic habitat have been affected by trace-element-contaminated sediment that moves from mine wastes into and down streams during snowmelt and storm runoff events within the Boulder River watershed. Present-day trace element concentrations in the streambed sediments and fluvial tailings have been extensively studied. However, in order to accurately evaluate the impact of mining on the stream environments, it is also necessary to evaluate the pre-mining trace-element concentrations in the streambed sediments. Three types of samples have been collected for estimation of pre-mining concentrations: 1) streambed sediment samples from the Boulder River and its tributaries located upstream from historical mining activity, 2) stream terrace deposits located both upstream and downstream of the major tributaries along the Boulder River, and 3) cores through sediment in overbank deposits, in abandoned stream channels, or beneath fluvial tailings deposits. In this report, we present geochemical data for six stream-terrace samples and twelve sediment-core samples and lead isotopic data for six terrace and thirteen core samples. Sample localities are in table 1 and figures 1 and 2, and site and sample descriptions are in table 2. Geochemical data have been presented for cores through fluvial tailings on High Ore Creek, on upper Basin Creek, and on Jack Creek and Uncle Sam Gulch. Geochemical and lead isotopic data for modern streambed-sediment samples have been presented by Fey and others. Lead isotopic determinations in bed sediments have been shown to be an effective tool for evaluating the contributions from various sources to the metals in bed sediments. However, in order to make these calculations, the lead isotopic compositions of the contaminant sources must also be known. Consequently, we have determined the lead isotopic compositions of five streambed-sediment samples heavily contaminated with fluvial mine waste immediately downstream from large mines in the Boulder River watershed in order to determine the lead isotopic signatures of the contaminants. Summary geochemical data for the contaminants are presented here and geochemical data for the streambed-sediment samples are given by Fey and others. Downstream from the Katie mill site and Jib tailings, fluvial deposits of mill tailings are present on a 10-m by 50-m bar in the Boulder River below the confluence with Basin Creek. The source of these tailings is not known, but fluvial tailings are also present immediately downstream from the Katie mill site, which is immediately upstream from the confluence with Basin Creek. Nine cores of fluvial tailings from this bar were analyzed. Dendrochronology samples were taken at several stream terrace localities to provide age control on the stream terrace deposits. Trees growing on the surfaces of stream terraces provide a minimum age for the terrace deposits, although floods subsequent to the trees' growth could have deposited post-mining overbank deposits around the trees. Historical data were also used to provide estimates of minimum ages of cultural features and to bracket the age of events.

Montana↗

USGS2002

Data on surface-water, streambed-interstitial water, and bed-sediment quality for selected locations in the small arms impact area of central Fort Gordon, Georgia, September 4-6, 2001

In September 2001, the U.S. Geological Survey, in cooperation with the Environmental and Natural Resources Management Office of the U.S. Army Signal Center and Fort Gordon (U.S. Department of the Army), conducted a chemical assessment of surface water, streambed-interstitial water, and bed sediments within the small arms impact area of Fort Gordon Military Installation. The study was conducted in support of the development of an Integrated Natural Resources Management Plan (INRMP) for Fort Gordon, Georgia. An effective INRMP ensures that natural resources conservation measures and U.S. Army activities on the military base are integrated and consistent with Federal requirements to manage military installations on an ecosystem basis. Filtered water samples were collected from five sites along South Prong Creek and three sites along Marcum Branch Creek for chemical analyses of major ions, nutrients, and selected trace elements. On-site measurements of pH, temperature, specific conductance, and dissolved oxygen were made at the eight sites. Filtered water collected showed varying concentrations in both surface- and streambed-interstitial water. Bed-sediment samples collected from South Prong Creek contain elevated levels of arsenic, barium, beryllium, cadmium, chromium, cobalt, copper, iron, lead, manganese, nickel, selenium, vanadium, and total organic carbon relative to previous concentrations (McConnell and others, 2000). Bed-sediment samples collected from Marcum Branch Creek contain elevated levels of beryllium, copper, lead, manganese, mercury, selenium, and total organic carbon relative to previous concentrations (McConnell and others, 2000).

Georgia↗

USGS2005

Questa baseline and pre-mining ground-water quality invistigation. 13. Mineral microscopy and chemistry of mined and unmined porphyry molybdenum mineralization along the Red River, New Mexico: Implications for ground- and surface-water quality

This report is one in a series presenting results of an interdisciplinary U.S. Geological Survey (USGS) study of ground-water quality in the lower Red River watershed prior to open-pit and underground molybdenite mining at Molycorp's Questa mine. The stretch of the Red River watershed that extends from just upstream of the town of Red River to just above the town of Questa includes several mineralized areas in addition to the one mined by Molycorp. Natural erosion and weathering of pyrite-rich rocks in the mineralized areas has created a series of erosional scars along this stretch of the Red River that contribute acidic waters, as well as mineralized alluvial material and sediments, to the river. The overall goal of the USGS study is to infer the pre-mining ground-water quality at the Molycorp mine site. An integrated geologic, hydrologic, and geochemical model for ground water in the mineralized but unmined Straight Creek drainage is being used as an analogue for the geologic, geochemical, and hydrologic conditions that influenced ground-water quality and quantity at the mine site prior to mining. This report summarizes results of reconnaissance mineralogical and chemical characterization studies of rock samples collected from the various scars and the Molycorp open pit, and of drill cuttings or drill core from bedrock beneath the scars and adjacent debris fans.

New Mexico↗

USGS1979

Water quality of south San Francisco Bay and Coyote Creek after failure of the San Jose-Santa Clara Water Pollution Control Plant I. 17 September - 10 October 1979

Data are presented to document some short-term biological and chemical consequences of a sewage spill in the southern area of San Francisco Bay and its receiving-water tributary, Coyote Creek. Sampling was conducted at fixed U.S. Geological Survey stations in South Bay, and at six new stations in Coyote Creek, on 17, 20, 25, 26 September and 3, 10 October 1979. Measured water-quality parameters were: salinity; temperature; turbidity; concentrations of selected dissolved gases (oxygen, carbon dioxide, methane, nitrous oxide, ethylene, ethane); concentrations of dissolved inorganic nutrients (ammonia, nitrate, nitrite, phosphate, silicate); and concentrations of chlorophyll a and phaeopigments, total coliforms, fecal coliforms, and fecal streptococci. Rates of oxygen utilization and photosynthetic production were measured at selected stations.

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