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At least 307 records · Page 17Linked to original sources

USGS2026

Multiple-well monitoring site adjacent to the Midway- Sunset and Buena Vista Oil Fields, Kern County, California

Groundwater quality in and around oil fields in the Southern San Joaquin Valley is of interest to many California residents that rely heavily on groundwater for domestic, commercial, and agricultural use. To help assess the effects of historical oil-field activities and natural geologic sources on groundwater near the southwest margins of the Kern County Groundwater Subbasin, a multiple-well monitoring site was installed near the administrative boundary between the Midway-Sunset and Buena Vista Oil Fields in Kern County, California. The installation of the Midway-Sunset Buena Vista multiple-well monitoring site (MSBV) supports regional analysis of the relations of oil and gas sources to groundwater quality by providing information about the geology, hydrology, geophysical properties, and water quality of the alluvial and upper Tulare aquifers in areas where groundwater data were limited. Data collected from the site included drill cuttings, whole core samples, sidewall core samples, mud-gas analysis, borehole geophysical logs, depth to water measurements, and water quality samples. Whole cores were scanned using dual energy computed tomography. Subsamples of selected cores were analyzed for density, porosity, specific retention, and bulk minerology. Thin sections of the subsamples were prepared, photographed, and examined. Two samples were analyzed using scanning electron microscope technology to examine the microporosity of diatomite laden sediment. Instrumentation installed in the wells collect hourly depth to water measurements. Analysis of the data show there is 355 feet of alluvium overlying the Tulare Formation at the well site. The contact between the two formations is an aquitard resulting in a perched aquifer in the alluvium and unconfined aquifer in the Tulare Formation. The alluvium is more heterogenous and finer grained than the Tulare Formation resulting in markedly higher porosity in the alluvium compared to the Tulare Formation. Higher specific retention observed in the alluvium is attributed to the finer grained sediment and greater abundance of reworked diatomite (as represented by opal-CT [cristobalite-tridymite]) compared to the Tulare Formation. Total dissolved solids (TDS) approached or exceeded 10,000 milligrams per liter (mg/L) in the alluvium from approximately 176 to 242 feet below land surface and at the top of the Amnicola clay at approximately 670 feet below land surface within the Tulare Formation. Elevated TDS, chloride, and boron concentrations in the alluvium and on top of the Amnicola clay likely reflect groundwater that is mixed with oil-field water. Water chemistry and modern-aged groundwater in the alluvial monitoring well (MSBV #3) are consistent with the oil-field water in the alluvium being derived from documented historical surface disposal of oil-field water upslope (northwest) of the site. Water chemistry and pre-modern groundwater age in the deeper Tulare monitoring well (MSBV #1) on top of the Amnicola clay are consistent with oil-field fluids derived from upslope natural geologic sources or old oil wells that leak in the subsurface. Shallow groundwater in the Tulare (MSBV #2) is not affected by mixing with oil-field sources.

EarthArXiv↗

USGS2021

The Biscuit Brook and Neversink Reservoir Watersheds: Long-term investigations of stream chemistry, soil chemistry, and aquatic ecology in the Catskill Mountains, New York, USA, 1983 to 2020

This data note describes the Biscuit Brook and Neversink Reservoir watershed Long-Term Monitoring Data that includes: 1) stream discharge, (1983 – 2020 for Biscuit Brook and 1937 – 2020 for the Neversink Reservoir watershed), 2) stream water chemistry, 1983-2020, at 4 stations, 3) fish survey data from 16 locations in the watershed 1990-2019, 4) soil chemistry data from 2 headwater sub-watersheds, 1993-2012, and 5) periodic stream water chemistry sampling data from 364 locations throughout the watershed, 1983-2020. The Neversink Reservoir watershed in the Catskill Mountains of New York, USA drains an area of 172.5 km 2 . The watershed feeds one of 6 reservoirs in New York City's West of Hudson water supply, which accounts for about 90% of the city's water supply. Biscuit Brook is a 9.63 km 2 tributary sub-watershed within the Neversink Reservoir watershed.

New York↗

USGS1994

Low cost limestone treatment of acid sensitive trout streams in the Appalachian Mountains of Virginia

The method of single point, single application liming has been studied as a means of mitigating anthropogenic acid in trout streams in Virginia. Three critically acid sensitive streams were dosed with a total of five applications of limestone sand and monitored before, during and after the treatments to assess changes in water chemistry and biota. Limestone treatments of 8 to 50 tons (particle sizes 150–1000 μ m), with the amounts based on sulfate deposition loading and existent stream water chemistry, were used to restore ‘lost’ acid neutralizing capacity (ANC). Contact time between the limestone bed in the stream bottom and the water was the limiting factor affecting the degree of treatment with bed length primarily controlled by the gradient of the stream at the dosing site. A single site application was able to restore approximately 2/3 of the ANC. Exponential fits of limestone consumption data were used to predict that treaments of similar streams would last from two five years before reliming was necessary. Both total and monomeric aluminum levels were reduced up to 50%, and aquatic biota increased below the treatment sites. Post-liming average values for the three streams were pH 6.66, 82.7 μ eq L −1 ANC and 2.63 mg L −1 Ca. The average ANC improvement suggests that some 88% of the native trout streams in Virginia, which average 29 μ eq L −1 ANC reduction from acid deposition, could be temporarily restored using single application liming.

Virginia↗

USGS2010

Processes controlling the chemistry of two snowmelt‐dominated streams in the Rocky Mountains

Time‐intensive discharge and chemical data for two alpine streams in the Loch Vale watershed, Colorado, were used to identify sources of runoff, flow paths, and important biogeochemical processes during the 1992 snowmelt runoff season. In spite of the paucity of soil cover the chemical composition of the streams is regulated much as in typical forested watersheds. Soils and other shallow groundwater matrices such as boulder fields appear to be more important in controlling surface‐water chemistry than their abundance would indicate. The chemical composition of the major source waters (usually thought of as end‐members whose chemical composition is relatively constant over time) changes at the same time that their mixing ratio in streams changes, confounding use of end‐member mixing models to describe stream‐water chemistry. Changes in the chemical composition of these source waters are caused by the ionic pulse of solutes from the snowpack and the small size of the shallow groundwater reservoir compared to the volume of snowmelt passing through it. The brief hydrologic residence time in the shallow groundwater indicates that concentrations of most dissolved constituents of stream water were controlled by fast geochemical processes that occurred on timescales of hours to days, rather than slower processes such as weathering of primary minerals. Differences in the timing of snowmelt‐related processes between different areas of the watershed also affect the stream‐water chemical composition. Cirque lakes affect discharge and chemical composition of one of the streams; seasonal control on stream‐water NO 3 and SiO 2 concentrations by diatom uptake in the lakes was inferred. Elution of acidic waters from the snowpack, along with dilution of base cations originating in shallow groundwater, caused episodes of decreased acid‐neutralizing capacity in the streams, but the streams did not become acidic.

Colorado↗

USGS1989

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

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

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

USGS2012

A comparison of U.S. Geological Survey three-dimensional model estimates of groundwater source areas and velocities to independently derived estimates, Idaho National Laboratory and vicinity, Idaho

The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, evaluated a three-dimensional model of groundwater flow in the fractured basalts and interbedded sediments of the eastern Snake River Plain aquifer at and near the Idaho National Laboratory to determine if model-derived estimates of groundwater movement are consistent with (1) results from previous studies on water chemistry type, (2) the geochemical mixing at an example well, and (3) independently derived estimates of the average linear groundwater velocity. Simulated steady-state flow fields were analyzed using backward particle-tracking simulations that were based on a modified version of the particle tracking program MODPATH. Model results were compared to the 5-microgram-per-liter lithium contour interpreted to represent the transition from a water type that is primarily composed of tributary valley underflow and streamflow-infiltration recharge to a water type primarily composed of regional aquifer water. This comparison indicates several shortcomings in the way the model represents flow in the aquifer. The eastward movement of tributary valley underflow and streamflow-infiltration recharge is overestimated in the north-central part of the model area and underestimated in the central part of the model area. Model inconsistencies can be attributed to large contrasts in hydraulic conductivity between hydrogeologic zones. Sources of water at well NPR-W01 were identified using backward particle tracking, and they were compared to the relative percentages of source water chemistry determined using geochemical mass balance and mixing models. The particle tracking results compare reasonably well with the chemistry results for groundwater derived from surface-water sources (-28 percent error), but overpredict the proportion of groundwater derived from regional aquifer water (108 percent error) and underpredict the proportion of groundwater derived from tributary valley underflow from the Little Lost River valley (-74 percent error). These large discrepancies may be attributed to large contrasts in hydraulic conductivity between hydrogeologic zones and (or) a short-circuiting of underflow from the Little Lost River valley to an area of high hydraulic conductivity. Independently derived estimates of the average groundwater velocity at 12 well locations within the upper 100 feet of the aquifer were compared to model-derived estimates. Agreement between velocity estimates was good at wells with travel paths located in areas of sediment-rich rock (root-mean-square error [RMSE] = 5.2 feet per day [ft/d]) and poor in areas of sediment-poor rock (RMSE = 26.2 ft/d); simulated velocities in sediment-poor rock were 2.5 to 4.5 times larger than independently derived estimates at wells USGS 1 (less than 14 ft/d) and USGS 100 (less than 21 ft/d). The models overprediction of groundwater velocities in sediment-poor rock may be attributed to large contrasts in hydraulic conductivity and a very large, model-wide estimate of vertical anisotropy (14,800).

Idaho↗

USGS2014

Associations between water physicochemistry and Prymnesium parvum presence, abundance, and toxicity in west Texas reservoirs

Toxic blooms of golden alga ( Prymnesium parvum ) have caused substantial ecological and economic harm in freshwater and marine systems throughout the world. In North America, toxic blooms have impacted freshwater systems including large reservoirs. Management of water chemistry is one proposed option for golden alga control in these systems. The main objective of this study was to assess physicochemical characteristics of water that influence golden alga presence, abundance, and toxicity in the Upper Colorado River basin (UCR) in Texas. The UCR contains reservoirs that have experienced repeated blooms and other reservoirs where golden alga is present but has not been toxic. We quantified golden alga abundance (hemocytometer counts), ichthyotoxicity (bioassay), and water chemistry (surface grab samples) at three impacted reservoirs on the Colorado River; two reference reservoirs on the Concho River; and three sites at the confluence of these rivers. Sampling occurred monthly from January 2010 to July 2011. Impacted sites were characterized by higher specific conductance, calcium and magnesium hardness, and fluoride than reference and confluence sites. At impacted sites, golden alga abundance and toxicity were positively associated with salinity-related variables and blooms peaked at ~10°C and generally did not occur above 20°C. Overall, these findings suggest management of land and water use to reduce hardness or salinity could produce unfavorable conditions for golden alga.

Journal of the American Water Resources Associatio↗

USGS2018

Preliminary groundwater salinity mapping near selected oil fields using historical water-sample data, central and southern California

The distribution of groundwater salinity was mapped for 31 oil fields and adjacent aquifers and summarized by 8 subregions across major oil-producing areas of central and southern California. The objectives of this study were to describe the distribution of groundwater near oil fields having total dissolved solids less than 10,000 milligrams per liter (mg/L) based on available data and to document where data gaps exist. Salinity was represented by the measured or calculated concentration of total dissolved solids (TDS) in samples of produced water obtained from petroleum wells and groundwater obtained from water wells. The water chemistry data were used to estimate the minimum depths of TDS greater than 3,000 mg/L and greater than 10,000 mg/L in areas near selected oil fields using historical water-chemistry data coupled with available well-location and construction information. The 10,000 mg/L threshold, representing the highest level of TDS concentration of water that could be considered as a potential source of drinking water, was present in all but 4 (Jasmin, Kern Bluff, Kern Front, and Mount Poso) of the 31 individual oil fields. Among petroleum wells, the median TDS concentration of produced water ranged from 500 mg/L for the Jasmin field to 32,636 mg/L for the Elk Hills field. Among water wells, median TDS concentrations, either reported or calculated from specific conductance, ranged from 151 mg/L for wells within 2 miles of the Ten Section field to 9,750 mg/L for wells within 2 miles of the combined North and South Belridge fields. In general, TDS across the eight geographic subregions increased with depth, but the relation of TDS with depth varied regionally. The most pronounced increases in TDS with depth were across the West Kern Valley Floor and West Kern Valley Margin subregions on the west side of the San Joaquin Valley, and in the vicinity of the Wilmington field in the Los Angeles Basin subregion; in these areas, relatively high TDS concentrations greater than 10,000 mg/L were present within the upper few hundred to several thousand feet of land surface. Total dissolved solids concentrations increased more gradually with depth in the Middle Kern Valley Floor subregion, in the South Kern Valley Margin subregion, in the vicinity of the Montebello and Santa Fe Springs fields in the Los Angeles Basin subregion, and in the Central Coast Basin subregion. The Kern Sierran Foothills and East Kern Valley Floor subregions, on the east side of the San Joaquin Valley, had the most gradual increases in TDS with depth. Fields in the East Kern Valley Floor subregion generally had groundwater and produced water with TDS less than 10,000 mg/L that extended to a large depth compared to most other subregions. Overall, the west side of the San Joaquin Valley in Kern County and the Wilmington field in Los Angeles County generally have the highest TDS values and the shallowest depths to high TDS. High TDS at relatively shallow depths on the west side of the San Joaquin Valley may be because of a combination of natural conditions and anthropogenic factors. In the vicinity of the Wilmington field in the Los Angeles Basin subregion, high TDS at relatively shallow depths is attributable at least in part to seawater intrusion. Fields on the east side of the San Joaquin Valley in Kern County have the lowest TDS and greatest depths to TDS greater than 10,000 mg/L because of their geologic setting adjacent to Sierra Nevada recharge areas. Reconnaissance salinity mapping was limited by several factors. The primary limitation was the lack of well-construction data for a significant number of water wells. Bottom perforation, well depth, or hole depth were not available for 35 percent of wells used for salinity mapping. A second limitation was variability in data quality. Total dissolved solids and specific conductance data were compiled from different data sources with varying degrees of documentation that ranged from comprehensive to very little or none. As a result, it was not always possible to assess the quality of the provided data with respect to either conditions at each well during sampling or the methodology used for sample collection and analysis. A third limitation was the lack of wells, either petroleum or water, and associated TDS data over large vertical intervals for some fields. As a result, the distribution of salinity and the depths at which TDS concentration exceeds the 3,000 and 10,000 mg/L thresholds could not always be precisely determined. This analysis highlights key gaps that need to be filled with additional analysis of other sources of information, such as borehole geophysical logs and new water sample or geophysical data collection.

California↗

USGS2019

Hydraulic, geochemical, and thermal monitoring of an aquifer system in the vicinity of Mammoth Lakes, Mono County, California, 2015–17

Since 2014, the U.S. Geological Survey has been working in cooperation with the Bureau of Land Management, Mono County, Ormat Technologies, Inc., and the Mammoth Community Water District to design and implement a groundwater-monitoring program for the proposed Casa Diablo IV Geothermal Power Project in Long Valley Caldera, California, to characterize baseline groundwater-level, water-temperature, and water-chemistry conditions at dedicated monitoring wells and municipal supply wells. The publicly available data and the analyses provided here represent quality-assured and peer-reviewed information to help with the management of the thermal and non-thermal water resources beneath and in the vicinity of the town of Mammoth Lakes, California. The methods of data collection for continuous water levels and quarterly water-temperature profiles for two 600-foot-deep monitoring wells during 2016 through 2017 are discussed. Also discussed are the methods of water-sample collection and characterizations of the water chemistry in numerous wells in the multilayered aquifer system beneath Mammoth Lakes. Additionally, the methodology used to develop digital (mathematical) filters to remove or reduce the effects of barometric pressure and solid Earth tides on the continuous water-level records is discussed. Digitally filtered water levels for a 2017 flow test of a deep geothermal production well are described, and various aquifer responses observed during the flow test are discussed. These are further considered in a companion evaluation of potential physical and chemical influences on the water-level data collected during the flow test. The digitally filtered water-level data indicated that some hydraulic communication exists between the deep geothermal aquifer and shallow groundwater aquifer at the location of the flow test, northeast of Mammoth Lakes. Groundwater-chemistry data from three wells indicated that shallow groundwater naturally mixes with a small component of geothermal water along the northern periphery of the shallow aquifer system at Mammoth Lakes.

California↗

USGS1995

Geochemical processes in ground water resulting from surface mining of coal at the Big Sky and West Decker Mine areas, southeastern Montana

A potential hydrologic effect of surface mining of coal in southeastern Montana is a change in the quality of ground water. Dissolved-solids concen- trations in water in spoils aquifers generally are larger than concentrations in water in the coal aquifers they replaced; however, laboratory experiments have indicated that concentrations can decrease if ground water flows from coal-mine spoils to coal. This study was conducted to determine if decreases in concentrations occur onsite and, if so, which geochemical processes caused the decreases. Solid-phase core samples of spoils, unmined over- burden, and coal, and ground-water samples were collected from 16 observation wells at two mine areas. In the Big Sky Mine area, changes in ground- water chemistry along a flow path from an upgradient coal aquifer to a spoils aquifer probably were a result of dedolomitization. Dissolved-solids concentrations were unchanged as water flowed from a spoils aquifer to a downgradient coal aquifer. In the West Decker Mine area, dissolved-solids concentrations apparently decreased from about 4,100 to 2,100 milligrams per liter as water moved along an inferred flow path from a spoils aquifer to a downgradient coal aquifer. Geochemical models were used to analyze changes in water chemistry on the basis of results of solid-phase and aqueous geochemical characteristics. Geochemical processes postulated to result in the apparent decrease in dissolved-solids concentrations along this inferred flow path include bacterial reduction of sulfate, reverse cation exchange within the coal, and precipitation of carbonate and iron-sulfide minerals.

Montana↗

USGS2026

Summertime methane and carbon dioxide emission rates and associated variables from a national-scale survey of 146 reservoirs in the United States

Reservoirs are globally important sources of greenhouse gases, but the magnitude of their emissions is highly uncertain. Here we present data for 146 reservoirs from two surveys of reservoir methane and carbon dioxide emissions, one at the regional scale in the midwestern United States and one at the national scale in the conterminous United States, plus data from one reservoir in Washington and another in Puerto Rico. At all reservoirs, ebullitive and diffusive emissions and basic physiochemistry were measured at 15-70 locations during one 22 to 64-hour period during the summers of 2016-2023, with four reservoirs revisited a second time. Concomitant water chemistry measurements were also made at an index site. The dataset is comprised of two geospatial files and seven .csv files containing greenhouse gas emissions, water chemistry, morphology, and other relevant data. These data comprise the largest multi-reservoir emissions dataset ever assembled using consistent measurement methods.

conterminous United States, Puerto Rico↗

USGS2012

National hydrography dataset--linear referencing

Geospatial data normally have a certain set of standard attributes, such as an identification number, the type of feature, and name of the feature. These standard attributes are typically embedded into the default attribute table, which is directly linked to the geospatial features. However, it is impractical to embed too much information because it can create a complex, inflexible, and hard to maintain geospatial dataset. Many scientists prefer to create a modular, or relational, data design where the information about the features is stored and maintained separately, then linked to the geospatial data. For example, information about the water chemistry of a lake can be maintained in a separate file and linked to the lake. A Geographic Information System (GIS) can then relate the water chemistry to the lake and analyze it as one piece of information. For example, the GIS can select all lakes more than 50 acres, with turbidity greater than 1.5 milligrams per liter.

Fact Sheet↗

USGS2015

Suburban groundwater quality as influenced by turfgrass and septic sources, Delmarva Peninsula, USA

Suburban land use is expanding in many parts of the United States and there is a need to better understand the potential water-quality impacts of this change. This study characterized groundwater quality in a sandy, water-table aquifer influenced by suburban development and compared the results to known patterns in water chemistry associated with natural, background conditions and agricultural effects. Samples for nutrients, major ions, and isotopes of N and O in NO 3 − were collected in 2011 beneath turfgrass from 29 shallow wells (median depth 3.7 m) and from 18 deeper wells (median depth 16.9 m) in a long-term suburban development. Nitrate (as N) concentrations in groundwater beneath turfgrass were highly variable (0.02–22.3 mg L −1 ) with a median of 2.7 mg L −1 , which is higher than natural water chemistry (>0.4 mg L −1 ; Na + –Cl − –HCO 3 − water type), but significantly lower than concentrations beneath a nearby agricultural area (median 16.9 mg L −1 ; p < .0001). Dissolved Fe concentrations in shallow suburban groundwater, attributed to chelated Fe in turfgrass fertilizers, were significantly higher ( p < .005) than concentrations from the agricultural site, although a Ca 2+ –Mg 2+ –Cl − –NO 3 − water type was dominant in both areas. A Na + –Cl − –NO 3 − water type indicated a septic-system source for nitrate in deep suburban groundwater (0.06–6.0 mg L −1 ; median 1.5 mg L −1 ). Isotopic data indicated denitrification; however, geochemical techniques were more helpful in identifying nitrate sources. Results indicate that suburban expansion into agricultural areas may significantly decrease overall nitrate concentrations in groundwater, but excessive turfgrass fertilization could result in localized contamination.

Delaware↗

USGS2007

Chemical data for rock, sediment, biological, precipitate, and water samples from abandoned copper mines in Prince William Sound, Alaska

Introduction In the early 20th century, approximately 6 million metric tons of copper ore were mined from numerous deposits located along the shorelines of fjords and islands in Prince William Sound, Alaska. At the Beatson, Ellamar, and Threeman mine sites (fig. 1), rocks containing Fe, Cu, Zn, and Pb sulfide minerals are exposed to chemical weathering in abandoned mine workings and remnant waste piles that extend into the littoral zone. Field investigations in 2003 and 2005 as well as analytical data for rock, sediment, precipitate, water, and biological samples reveal that the oxidation of sulfides at these sites is resulting in the generation of acid mine drainage and the transport of metals into the marine environment (Koski and others, 2008; Stillings and others, 2008). At the Ellamar and Threeman sites, plumes of acidic and metal-enriched water are flowing through beach gravels into the shallow offshore environment. Interstitial water samples collected from beach sediment at Ellamar have low pH levels (to ~3) and high concentrations of metals including iron, copper, zinc, cobalt, lead, and mercury. The abundant precipitation of the iron sulfate mineral jarosite in the Ellamar gravels also signifies a low-pH environment. At the Beatson mine site (the largest copper mine in the region) seeps containing iron-rich microbial precipitates drain into the intertidal zone below mine dumps (Foster and others, 2008). A stream flowing down to the shoreline from underground mine workings at Beatson has near-neutral pH, but elevated levels of zinc, copper, and lead (Stillings and others, 2008). Offshore sediment samples at Beatson are enriched in these metals. Preliminary chemical data for tissue from marine mussels collected near the Ellamar, Threeman, and Beatson sites reveal elevated levels of copper, zinc, and lead compared to tissue in mussels from other locations in Prince William Sound (Koski and others, 2008). Three papers presenting results of this ongoing investigation of sulfide oxidation in Prince William Sound are in press. Koski and others (2008) provide an overview of rock alteration, surface water chemistry, and the distribution of metals at the Ellamar, Threeman, and Beatson mine sites. Based on a 60-day, stream-discharge experiment at Beatson in 2005, Stillings and others (2008) analyze changes in water chemistry during storm events and the flux of metals to the shoreline. Foster and others (2008) investigate the biomass and diversity of microbial communities present in surface waters (streams, seeps, pore waters) using fatty acid methyl ester (FAMES) data and principal component analysis. The publications cited above contain a subset of the total chemical data for rock, sediment, biological, precipitate, and water samples collected from the three mine sites in 2003 and 2005. The purpose of this report is the presentation of complete chemical data sets for all samples collected during the two field periods of fieldwork. Data for a small number of samples collected at two other mines (Schlosser and Fidalgo, fig. 1), visited in 2003, are also included in the tables.

Alaska↗

USGS2007

Chemical data for rock, sediment, biological, precipitate, and water samples from abandoned copper mines in Prince William Sound, Alaska

In the early 20th century, approximately 6 million metric tons of copper ore were mined from numerous deposits located along the shorelines of fjords and islands in Prince William Sound, Alaska. At the Beatson, Ellamar, and Threeman mine sites (fig. 1), rocks containing Fe, Cu, Zn, and Pb sulfide minerals are exposed to chemical weathering in abandoned mine workings and remnant waste piles that extend into the littoral zone. Field investigations in 2003 and 2005 as well as analytical data for rock, sediment, precipitate, water, and biological samples reveal that the oxidation of sulfides at these sites is resulting in the generation of acid mine drainage and the transport of metals into the marine environment (Koski and others, 2008; Stillings and others, 2008). At the Ellamar and Threeman sites, plumes of acidic and metal-enriched water are flowing through beach gravels into the shallow offshore environment. Interstitial water samples collected from beach sediment at Ellamar have low pH levels (to ~3) and high concentrations of metals including iron, copper, zinc, cobalt, lead, and mercury. The abundant precipitation of the iron sulfate mineral jarosite in the Ellamar gravels also signifies a low-pH environment. At the Beatson mine site (the largest copper mine in the region) seeps containing iron-rich microbial precipitates drain into the intertidal zone below mine dumps (Foster and others, 2008). A stream flowing down to the shoreline from underground mine workings at Beatson has near-neutral pH, but elevated levels of zinc, copper, and lead (Stillings and others, 2008). Offshore sediment samples at Beatson are enriched in these metals. Preliminary chemical data for tissue from marine mussels collected near the Ellamar, Threeman, and Beatson sites reveal elevated levels of copper, zinc, and lead compared to tissue in mussels from other locations in Prince William Sound (Koski and others, 2008). Three papers presenting results of this ongoing investigation of sulfide oxidation in Prince William Sound are in press. Koski and others (2008) provide an overview of rock alteration, surface water chemistry, and the distribution of metals at the Ellamar, Threeman, and Beatson mine sites. Based on a 60-day, stream-discharge experiment at Beatson in 2005, Stillings and others (2008) analyze changes in water chemistry during storm events and the flux of metals to the shoreline. Foster and others (2008) investigate the biomass and diversity of microbial communities present in surface waters (streams, seeps, pore waters) using fatty acid methyl ester (FAMES) data and principal component analysis. The publications cited above contain a subset of the total chemical data for rock, sediment, biological, precipitate, and water samples collected from the three mine sites in 2003 and 2005. The purpose of this report is the presentation of complete chemical data sets for all samples collected during the two field periods of fieldwork. Data for a small number of samples collected at two other mines (Schlosser and Fidalgo, fig. 1), visited in 2003, are also included in the tables.

Alaska↗

USGS2008

Influence of flow-through and renewal exposures on the toxicity of copper to rainbow trout

We examined changes in water chemistry and copper (Cu) toxicity in three paired renewal and flow-through acute bioassays with rainbow trout (Oncorhynchus mykiss). Test exposure methodology influenced both exposure water chemistry and measured Cu toxicity. Ammonia and organic carbon concentrations were higher and the fraction of dissolved Cu lower in renewal tests than in paired flow-through tests. Cu toxicity was also lower in renewal tests; 96 h dissolved Cu LC50 values were 7-60% higher than LC50s from matching flow-through tests. LC50 values in both types of tests were related to dissolved organic carbon (DOC) concentrations in exposure tanks. Increases in organic carbon concentrations in renewal tests were associated with reduced Cu toxicity, likely as a result of the lower bioavailability of Cu-organic carbon complexes. The biotic ligand model of acute Cu toxicity tended to underpredict toxicity in the presence of DOC. Model fits between predicted and observed toxicity were improved by assuming that only 50% of the measured DOC was reactive, and that this reactive fraction was present as fulvic acid. ?? 2007 Elsevier Inc. All rights reserved.

Ecotoxicology and Environmental Safety↗

USGS1999

Environmental characteristics and water quality of hydrologic benchmark network stations in the Eastern United States, 1963-95

The information in this report was compiled to aid in the application and interpretation of historical water-quality data collected as part of the U.S. Geological Survey Hydrologic Benchmark Network program, which was established in 1963 to provide long-term measurements of streamflow and water quality in areas that are minimally affected by human activities. This report describes the environmental characteristics and water quality at 16 benchmark basins in the Eastern United States. In most of the basins, stream-water chemistry seems to be controlled by the interaction of acidic precipitation with the underlying soils and bedrock. Land use had a minimal effect on stream-water chemistry at most of the gaging stations.

Circular↗

USGS2000

Methodology for applying monitored natural attenuation to petroleum hydrocarbon-contaminated ground-water systems with examples from South Carolina

Natural attenuation processes such as dispersion, advection, and biogradation serve to decrease concentrations of disssolved contaminants as they are transported in all ground-water systems. However, the efficiency of these natural attenuation processes and the degree to which they help attain remediation goals, varies considerably from site to site. This report provides a methodology for quantifying various natural attenuation mechanisms. This methodology incorporates information on (1) concentrations of contaminants in space and/or time; (2) ambient reduction/oxidation (redox) conditions; (3) rates and directions of ground-water flow; (4) rates of contaminant biodegradation; and (5) demographic considerations, such as the presence of nearby receptor exposure points or property boundaries. This document outlines the hydrologic, geochemical, and biologic data needed to assess the efficiency of natural attenuation, provides a screening tool for making preliminary assessments, and provides examples of how to determine when natural attenuation can be a useful component of site remediation at leaking underground storage tank sites. At a site in the Piedmont Physiographic Province (Laurens, South Carolina), hydrologic and water-chemistry data indicate that the natural attenuation capacity for benzene is approximately 5 percent per foot of flowpath. As a result, benzene concentrations would decrease from about 28,000 micrograms per liter in ground water at the source area to less than 5 micrograms per liter 200 feet downgradient and prior to discharging to a stream. Because of this rapid attenuation, contaminants do not presently impact the stream downgradient of the site. In contrast, at a site in the coastal Plain Physiographic Province (Charleston, South Carolina), hydrologic and water-chemistry data indicate that, even thought the site has a substantial natural attenuation capacity, it may not be sufficient to fully protect a nearby point of ground-water discharge. These two sites illustrate how the efficiency of natural attenuation processes acting on petroleum hydrocarbons can be systematically evaluated using hydrologic, geochemical, and microbiologic methods. These methods, in turn, can be used to assess the role that the natural attenuation of petroleum hydrocarbons can play in achieving overall site remediation.

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