Search USGSSearch

SEARCH · Search USGS

Results for “EPA Report”

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

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

At least 73 records · Page 4Linked to original sources

Chemical constituent concentrations in stream water, streambed sediment, and soils of Fort Belvoir, Virginia—A characterization of ambient conditions in 2019

Introduction The U.S. Army Fort Belvoir (FTBL) installation is on the banks of the Potomac River in Fairfax County, northeastern Virginia. The installation was founded by the U.S. Army during World War I. It has been home to a variety of military organizations over the course of its more than 100-year history and currently houses more than 145 mission partners. The installation consists of two noncontiguous units, the Main Post, and a smaller area to the northwest, Fort Belvoir North Area (FTNA). FTBL encompasses 8.91 square miles. There is concern that activities on FTBL, including a long history of training, operations, and maintenance, may have resulted in contamination of stream water, streambed sediment, and (or) soils. Of particular concern is the U.S. Environmental Protection Agency (EPA) Target Analyte List (TAL). TAL refers to “the list of inorganic compounds/elements designated for analysis as contained in the version of the EPA Contract Laboratory Program Statement of Work for Inorganics Analysis, Multi-Media, Multi-Concentration in effect as of the date on which the laboratory is performing the analysis” ( https://www.nj.gov/dep/srp/guidance/tcl_tal/ ). Because of the potential for TAL contamination at FTBL, the U.S. Geological Survey (USGS), in cooperation with U.S. Army Fort Belvoir, conducted a survey of FTBL’s stream water, streambed sediment, and soils during calendar year 2019. The terminology “ambient concentrations” is used in this report to represent the concentrations of the TAL and other constituents at the time of sampling. This is in contrast to “background concentrations,” a term that “refers to areas in which the concentrations of chemicals have not been elevated by site activities”. Although some of the samples collected for this project may represent “background concentrations,” there is no assurance that they do, so all data collected are described as having “ambient concentrations.” The purpose of the study was to obtain environmental data to characterize ambient concentrations of EPA TAL constituents in stream water, streambed sediment, and soils in FTBL, Virginia. This report describes methods and results of sampling stream water, streambed sediment, and soils during 2019. The purpose of this report is four-fold: (1) to describe the field sampling methods used to collect stream water, streambed sediment, and soils; (2) to describe the laboratory methods used to analyze the samples; (3) to report summaries of the field and laboratory results; and (4) to report the quality assurance and quality control results.

Virginia

Ground-water quality in east-central New Jersey, and a plan for sampling networks

Groundwater quality was evaluated in seven confined aquifers and the water table aquifer in east-central New Jersey based on 237 analyses of samples collected in 1981-82, and 225 older analyses. Investigation of the effect of land use on water quality and several sampling network proposals for the region are reported. Generally, water in the confined aquifers is of satisfactory quality for human consumption and most other uses. Iron (Fe) and manganese (Mn) concentrations exceed U.S. EPA drinking water standards in some wells screened in the Potomac-Raritan-Magothy aquifer system. Sodium (Na) concentrations in samples from three wells more than 800 ft deep in the Englishtown aquifer exceed the standard. Iron and Mn concentrations in this aquifer may also exceed the standards. Iron concentrations in the Wenonah-Mount Laurel aquifer exceed the standard. Based on 15 analyses of water from the Vincetown aquifer, Mn is the only constituent that exceeds the drinking water standard. In the Manasquan aquifer, 4 of the 16 Na determinations exceed the standard, and 8 of 16 Fe determinations exceed the standard. Water quality in the Atlantic City 800-ft sand is generally satisfactory. However, 12 Fe and 1 of 12 Mn determinations exceed the standards. For the Rio Grande water-bearing zone, 1 of 3 Fe determinations exceed the standard. The Kirkwood-Cohansey aquifer system (the water table aquifer) was the most thoroughly sampled (249 chemical analyses from 209 wells). Dissolved solids, chloride, Fe, nitrate, and Mn concentrations exceed drinking water standards in some areas. The results of chi-square tests of constituent distributions based on analyses from 158 wells in the water table aquifer indicate that calcium is higher in industrial and commercial areas; and Mg, chloride, and nitrate-plus-nitrite is higher in residential areas. (Author 's abstract)

Water-Resources Investigations Report

Status of selenium in south San Francisco Bay—A basis for modeling potential guidelines to meet National tissue criteria for fish and a proposed wildlife criterion for birds

The U.S. Environmental Protection Agency (EPA) proposed Aquatic Life and AquaticDependent Wildlife Criteria for Selenium (Se) in California’s San Francisco Bay and Delta (Bay-Delta) in June 2016. Here we apply the same modeling methodology—Ecosystem-Scale Selenium Modeling— to an assessment of conditions and documentation of food webs of south San Francisco Bay (South Bay) as an exploratory framework in support of site-specific Se criteria development. Long-term datasets contribute to the basis for modeling, especially the 21-year collection of the clam Macoma petalum from a mudflat at the lower end of South Bay (Lower South Bay). As such, this is a working document that may serve as a basis to establish an understanding of the specifics of Se biodynamics within the estuary and reduce uncertainties about how to protect it. This approach brings together the main factors involved in toxicity: likelihood of high exposure, inherent species sensitivity, and the behavioral ecology (for example, demographics and life history) of an organism in terms of susceptibility to a reproductive toxicant. Species sensitivity is represented here by use of the EPA’s current national tissue Se criterion for fish or that proposed to protect the eggs of aquatic birds for the Bay-Delta (U.S. Environmental Protection Agency, 2016a, 2016b, 2016c). This report also strives to bring together findings and field data across a body of literature for South Bay to provide an integrative assessment. We find an assemblage of site-specific conditions that could affect modeling: associated urban processes such as discharges from municipal wastewater treatment plants and drainage from mercury (Hg) mining and limestone extraction are sources of Se that characterize the Lower South Bay as the location of interest for Se exposure; • hydrodynamics are lagoon-like (that is, less flushing), which sustains elevated nutrients and phytoplankton blooms; • managed freshwater sources are a major hydrodynamic component; • birds, in addition to fish, are prominent predators in South Bay; • wetland restoration has recently intervened to play a significant role in ecosystem function that may include uptake of both Hg and Se; • the dietary food web of surficial-sediment to M. petalum is important because of the dominance of this clam species and its elevated Se bioaccumulation potential compared to other local food webs; and 2 • maximal Se concentrations may be limited by transitory or annually renewed food webs (for example, migratory shorebirds and decimation of clams from marshes). We also find that the constructed mechanistic model: • spatially connects to the Palo Alto mudflat site because of data availability; • accurately predicts average observed Se concentrations in M. petalum and in predator species of fish and birds; and • is able to bracket a range of potential protective water-column Se concentrations specific to predator species based on the EPA’s national Se criterion for whole-body fish tissue and a proposed site-specific criterion for bird eggs in the Bay-Delta.

California

Chemical characteristics and temporal trends in eight streams of the Catskill Mountains, New York

Discharge to concentration relationships for eight streams studied by the U.S. Geological Survey (USGS) as part of the U.S. Environmental Protection Agency's (U.S. EPA) Long-Term Monitoring Project (1983-89) indicate acidification of some streams by H2SO4 and HNO3 in atmospheric deposition and by organic acids in soils. Concentrations of major ions in precipitation were similar to those reported at other sites in the northeastern United States. Average concentrations of SO42- and NO3- were similar among streams, but base cation concentrations differed widely, and these differences paralleled the differences in acid neutralizing capacity (ANC). Baseflow ANC is not a reliable predictor of stream acidity at high flow; some streams with high baseflow ANC (> 150 ??eq L-1) declined to near zero ANC at high flow, and one stream with low baseflow ANC (< 50 ??eq L-1) did not approach zero ANC as flow increased. Episodic decreases in ANC and pH during peak flows were associated with increased concentrations of NO3- and dissolved organic carbon (DOC). Aluminum concentrations exceeding 300 ??g L-1 were observed during peak flows in headwater streams of the Neversink River and Rondout Creek. Seasonal Kendall Tau tests for temporal trends indicate that SO42- concentrations in streamwater generally decreased and NO3- concentrations increased during the period 1983-1989. Combined acid anion concentrations (SO42- + NO3-) were generally unchanged throughout the period of record, indicating both that the status of these streams with respect to acidic deposition is unchanged, and that NO3- is gradually replacing SO42- as the dominant acid anion in the Catskill streams.Discharge to concentration relationships for eight streams studied by the US Geological Survey (USGS) as part of the Environmental Protection Agency's (US EPA) Long-term monitoring project (19831-89) indicate acidification of some streams by H2SO4 and HNO3 in atmospheric deposition and by organic acids in soils. Concentrations of major ions in precipitations were similar to those reported at other sites in the northeastern United States. Average concentrations of SO42- and No3- were similar among streams, but base cation concentrations differed widely, and these differences parallelel the differences in acid neutralizing capacity (ANC).

Water, Air, & Soil Pollution

Mercury export from the Yukon River Basin and potential response to a changing climate

We measured mercury (Hg) concentrations and calculated export and yield from the Yukon River Basin (YRB) to quantify Hg flux from a large, permafrost-dominated, high-latitude watershed. Exports of Hg averaged 4400 kg Hg yr -1 . The average annual yield for the YRB during the study period was 5.17 &mu;g m -2 yr -1 , which is 3&ndash;32 times more than Hg yields reported for 8 other major northern hemisphere river basins. The vast majority (90%) of Hg export is associated with particulates. Half of the annual export of Hg occurred during the spring with about 80% of 34 samples exceeding the U.S. EPA Hg standard for adverse chronic effects to biota. Dissolved and particulate organic carbon exports explained 81% and 50%, respectively, of the variance in Hg exports, and both were significantly ( p < 0.001) correlated with water discharge. Recent measurements indicate that permafrost contains a substantial reservoir of Hg. Consequently, climate warming will likely accelerate the mobilization of Hg from thawing permafrost increasing the export of organic carbon associated Hg and thus potentially exacerbating the production of bioavailable methylmercury from permafrost-dominated northern river basins.

Alaska

Core descriptions, core photographs, physical property logs and surface textural data of sediment cores recovered from the continental shelf of the Monterey Bay National Marine Sanctuary during the research cruises M-1-95-MB, P-2-95-MB, and P-1-97-MB

In response to the 1992 creation of the Monterey Bay National Marine Sanctuary (MBNMS), the United States Geological Survey (USGS) initiated a multiyear investigation of the Sanctuary continental margin. As part of the investigative effort, this report summarizes the shipboard procedures, subsequent laboratory analyses, and data results from three seafloor sampling cruises conducted on the continental shelf between Monterey peninsula, CA and San Francisco, CA. The cruises were conducted in 1995 aboard the NOAA Ship McArthur (M-1-95-MB) and in 1995 and 1997 aboard the R/V Point Sur (P-2-95-MB and P-1-97-MB). Scientists and representatives from the Environmental Protection Agency (EPA), the National Oceanic and Atmospheric Administration (NOAA), the California Department of Fish and Game (CDFG), the University of California Santa Cruz (UCSC), and the San Jose State University Moss Landing Marine Laboratory (SJSU-MLML) supported the research effort. In this report we present sediment descriptions, sediment textural data, physical property logs, station metadata, and photographs of subcores from a total of three hundred and eighty four sample stations. At these sites either a box corer, MultiCore™r, grab sampler or a combination of these sampling devices were used to collect the sea floor sediments. The report is presented in an interactive web-based format with each mapped core station linked to the corresponding description and photo, and to a spreadsheet of surface texture and other sampling data.

California

The US EPA’s National Nutrient Inventory: Critical shifts in US nutrient pollution sources from 1987 to 2017

Efforts to constrain the negative environmental impacts of excess nitrogen (N) and phosphorus (P) are costly and challenging, due in part to inconsistent reporting of nutrient sources at temporal and spatial scales relevant for local decision making. To meet this challenge, the U.S. Environmental Protection Agency’s National Nutrient Inventory provides estimates of major agricultural, urban, atmospheric, and natural nutrient fluxes for the contiguous United States at county and HUC12 scales annually from 1987 (from 1950 for agriculture) to 2017. Since the late 1980s, total N emissions and atmospheric N deposition have declined 22% and 15%, respectively, despite increased agricultural emissions. Over the same period, municipal wastewater N and P loads remained largely stable, despite population increases, through wastewater treatment upgrades and the phaseout of phosphorus-containing detergents. Improved agricultural efficiency allowed for dramatic increases in agricultural production and crop harvest since 1987 (∼25% for N and P), with little change in surplus nutrients left on fields. Overall, a combination of innovative technologies and management has stemmed or even decreased major sources of nutrient pollution to the environment over the last several decades, representing an important shift that, if continued, may contribute to improved air, land, and water quality and human health.

contiguous United States

Groundwater conditions in Utah, spring of 2010

This is the forty-seventh in a series of annual reports that describe groundwater conditions in Utah. Reports in this series, published cooperatively by the U.S. Geological Survey and the Utah Department of Natural Resources, Division of Water Resources and Division of Water Rights, and the Utah Department of Environmental Quality, Division of Water Quality, provide data to enable interested parties to maintain awareness of changing groundwater conditions. This report, like the others in the series, contains information on well construction, groundwater withdrawal from wells, water-level changes, precipitation, streamflow, and chemical quality of water. Information on well construction included in this report refers only to wells constructed for new appropriations of groundwater. Supplementary data are included in reports of this series only for those years or areas which are important to a discussion of changing groundwater conditions and for which applicable data are available. This report includes individual discussions of selected significant areas of groundwater development in the State for calendar year 2009. Most of the reported data were collected by the U.S. Geological Survey in cooperation with the Utah Department of Natural Resources, Division of Water Resources and Division of Water Rights, and the Utah Department of Environmental Quality, Division of Water Quality. This report is also available online at http://www. waterrights.utah.gov/techinfo/ and http://ut.water.usgs.gov/ publications/GW2010.pdf. Groundwater conditions in Utah for calendar year 2008 are reported in Burden and others (2009) and available online at http://ut.water.usgs.gov/publications/ GW2009.pdf. Analytical results associated with water samples collected from each area of groundwater development were compared to State of Utah maximum contaminant levels (MCLs) and secondary drinking-water standards of routinely measureable substances present in water supplies. The MCLs and secondary drinking-water standards can be accessed online at http://www.rules.utah.gov/publicat/code/r309/r309-200. htm#T5. The U.S. Environmental Protection Agency (EPA) drinking-water standards can be accessed at http://www.epa. gov/safewater/mcl.html#mcls. Maximum contaminant levels and secondary drinking-water standards were developed for public water systems and do not apply to the majority of wells sampled during this study. Every 5 years, this report series includes maps depicting comparisons of 30-year changes in water levels for each of the major areas of groundwater development. The water-level change maps in this report show the difference between water levels measured in 1980 and in 2010. Water-level rises or declines occurring on shorter time scales are shown in plots of annual water-level measurements for several wells in each of the major areas of groundwater development.

Utah

Fort Collins Science Center

The U.S. Geological Survey's Fort Collins Science Center (FORT) is one of 17 USGS biological science centers nationwide. FORT conducts research and develops technical applications to assist land managers in understanding and managing biological resources, habitats, and ecosystems. Although the majority of FORT's activities are conducted within the 15-state Central Region of the USGS, many FORT projects are national or international in scope. FORT serves all Department of the Interior land management bureaus and other natural resource agencies. In addition, FORT scientists partner with DOI and other federal entities such as CDC, DOE, EPA, NASA, NIH, and USDA to share expertise and resources. FORT also partners with several universities and works cooperatively with states and nongovernmental organizations. Products and services include reports and publications, predictive models and software, maps and GIS products, and other technical assistance in the form of meetings, workshops, training, field visits, and needs assessments.

Fact Sheet

Groundwater quality, age, and susceptibility and vulnerability to nitrate contamination with linkages to land use and groundwater flow, Upper Black Squirrel Creek Basin, Colorado, 2013

The Upper Black Squirrel Creek Basin is located about 25 kilometers east of Colorado Springs, Colorado. The primary aquifer is a productive section of unconsolidated deposits that overlies bedrock units of the Denver Basin and is a critical resource for local water needs, including irrigation, domestic, and commercial use. The primary aquifer also serves an important regional role by the export of water to nearby communities in the Colorado Springs area. Changes in land use and development over the last decade, which includes substantial growth of subdivisions in the Upper Black Squirrel Creek Basin, have led to uncertainty regarding the potential effects to water quality throughout the basin. In response, the U.S. Geological Survey, in cooperation with Cherokee Metropolitan District, El Paso County, Meridian Service Metropolitan District, Mountain View Electric Association, Upper Black Squirrel Creek Groundwater Management District, Woodmen Hills Metropolitan District, Colorado State Land Board, and Colorado Water Conservation Board, and the stakeholders represented in the Groundwater Quality Study Committee of El Paso County conducted an assessment of groundwater quality and groundwater age with an emphasis on characterizing nitrate in the groundwater. Groundwater-quality samples were collected from 50 randomly selected wells between May and June 2013. The samples were analyzed for major ions, nutrients, dissolved gases, tritium ( 3 H), chlorofluorocarbons (CFC-11, CFC-12, and CFC-113), and fuel products (such as benzene, toluene, ethylbenzene, and xylenes). None of the groundwater samples exceeded the U.S. Environmental Protection Agency (EPA) National Primary Drinking Water Regulations for primary maximum contaminant levels (MCL) for major ions. Secondary maximum contaminant levels, which are not health concerns and affect mainly taste, color, or odor of the water, were observed in rare instances for pH (2 samples), chloride (1 sample), iron (3 samples), and manganese (8 samples). The secondary maximum contaminant level for total dissolved solids was also exceeded for two samples. Nitrate (nitrite plus nitrate as nitrogen in groundwater) was elevated above the estimated background concentration of natural recharge waters of 1 milligram per liter (mg/L) in 44 of the 50 wells sampled and showed a median concentration of 5.4 mg/L. Nitrate concentrations were above the MCL of 10 mg/L in 5 of the 50 wells sampled and above half of the EPA MCL (5 mg/L) in 27 of the 50 wells sampled, which included samples above the MCL. Dissolved-oxygen concentrations exceeded 0.5 mg/L in 95 percent of reported values (40 of 42 samples) and exceeded 2.0 mg/L in 90 percent of reported values (38 of 42 samples). The oxidized conditions observed in most areas indicate that nitrate from fertilizers and animal or human waste was geochemically stable and could persist in the groundwater for decades or perhaps longer. A historical analysis of median nitrate concentrations over nearly three decades showed an increase in nitrate of approximately 1 mg/L from 4.3 to 5.4 mg/L, although the increase was not determined to be significantly different using nonparametric statistical methods. Major-ion data indicate that groundwater representative of the primary aquifer was classified as calcium-sodium bicarbonate type water. Other water samples from wells located mainly along the periphery of the primary aquifer had cation-anion compositions consistent with distinct water sources, including groundwater contributions from the underlying bedrock aquifers. The areas with differentiable water sources were located mainly where alluvial deposits were thin and geologic contacts to the underlying bedrock aquifers were relatively shallow. Nitrate concentrations in the groundwater were evaluated for relations to land use. An agricultural region was defined using a sequence of land satellite imagery. Groundwater flow directions interpreted from median water-table elevations measured from 2000 to 2013 were used in conjunction with cropland locations to define the agricultural region boundaries by encompassing potential pathways of nitrate transport in the groundwater from nitrogen-based fertilizers. A statistically significant higher median nitrate concentration was observed for areas inside the agricultural region (6.7 mg/L) compared to areas outside the agricultural region (2.3 mg/L), although median concentrations in both areas were below the MCL (10 mg/L). Median nitrate concentration was also significantly greater in land parcels with septic use (4.9 mg/L) compared to nonseptic parcels (1.7 mg/L). In general, agriculture or septic use was identified as the primary source of nitrate, depending on location, while commercial, county, grazing, and residential land uses were generally secondary sources of nitrate. Apparent groundwater ages were estimated from chlorofluorocarbons (CFC-11, CFC-12, and CFC-113) and tritium ( 3 H) data using models that assumed piston flow and binary mixing (dilution of a young component with old, tracer-free water). The mean and median groundwater ages were about 30 years and the standard deviation was 6 years, indicating that most groundwater in the primary aquifer was &ldquo;young&rdquo; water that had recharged to the aquifer over the last few decades (post-1950s). The median fraction of young water was about 71 percent, and the standard deviation was 29 percent. The remaining water predated the 1950s, which may have originated from deeper geologic formations or may represent slow moving groundwater within the primary aquifer. Some of the oldest groundwater ages (older than 30 years) were observed in the upper reaches of the aquifer to the northwest where the primary aquifer is thin and intersects bedrock, supporting the hypothesis of geochemically distinct groundwater entering the primary aquifer from below. Groundwater that had reached the central part of the aquifer from upgradient areas of the basin was variable in age because of differences in flow paths and travel velocities. The groundwater age analysis showed that current (2013) land-use practices could affect water quality over decades to come, and that responses to remedial actions could be slow, especially for constituents, such as nitrate, that are stable under oxidized conditions. Fuel products (including acetone, benzene, diisopropyl ether, ethylbenzene, methyl acetate, methyl tertiary butyl ether (MTBE), methyl tert-pentyl ether, m- + p-xylene, o-xylene, tert-amyl alcohol, tert-butyl alcohol, tert-butyl ethyl ether, and toluene) were analyzed in groundwater from 49 of the 50 wells. Water from seven sites had detections for fuel compounds; all concentrations were below MCL. The results provided assurance of water quality and a valuable baseline to evaluate future trends of fuel constituents as the region is further developed. Probability maps were developed from logistic regression models to examine the likelihood that nitrate concentrations in groundwater exceeded specified levels. Susceptibility analysis examined relations between mid-level (5.0 mg/L) nitrate concentrations and climatic, hydrologic, and geologic variables; the significant variables were identified as depth to groundwater, soil organic matter, and soil water storage to 25-centimeter (cm) depth. The vulnerability assessments included natural factors driving susceptibility but also human factors related to land use and septic use. Vulnerability to low-level (2.5 mg/L) nitrate was related to depth to groundwater, septic zoning, and soil organic matter. The results highlighted that septic zoning affected low-level nitrate concentrations. Vulnerability to mid-level (5.0 mg/L) nitrate was examined using all 50 samples and also with two data outliers removed, which showed relatively high nitrate concentrations but also anomalous water chemistry or were located beyond the primary study area. Vulnerability to mid-level (5.0 mg/L) nitrate using all 50 samples was related to depth to groundwater, land use, septic use within a 500-meter (m) radius, soil water storage to a 25-cm depth, soil organic matter, and whether a location was within the agricultural region. The mid-level (5.0 mg/L) vulnerability model using 48 samples (two outliers removed) produced the best overall fit and was related to the same variables as when using all samples except septic use. The results for mid-level vulnerability provided additional support that septic use was associated with low levels of nitrate in the groundwater. Soil properties and land use were identified as the main drivers of moderate nitrate concentrations. Probabilities of exceeding low-level nitrate concentrations were high in most areas with the lowest probabilities usually to the northwest along thin geologic deposits in the upper part of the basin. The results of this investigation offer the foundational information needed for developing best management practices to mitigate nitrate contamination, basic concepts on water quality to aid public education, and information to guide regulatory measures if policy makers determine this is warranted. Science-based decision making will require continued monitoring and analysis of water quality in the future.

Colorado

Preliminary report on coal resources of the Wyodak-Anderson coal zone, Powder River Basin, Wyoming and Montana

The National Coal Resource Assessment (NCRA) project by the U.S. Geological Survey is designed to assess US coal with the greatest potential for development in the next 20 to 30 years. Coal in the Wyodak-Anderson (WA) coal zone in the Powder River Basin of Wyoming and Montana is plentiful, clean, and compliant with EPA emissions standards. This coal is considered to be very desirable for development for use in electric power generation. The purpose of this NCRA study was to compile all available data relating to the Wyodak- Anderson coal, correlate the beds that make up the WA coal zone, create digital files pertaining to the study area and the WA coal, and produce a variety of reports on various aspects of the assessed coal unit. This report contains preliminary calculations of coal resources for the WA coal zone and is one of many products of the NCRA study. Coal resource calculations in this report were produced using both public and confidential data from many sources. The data was manipulated using a variety of commercially available software programs and several custom programs. A general description of the steps involved in producing the resource calculations is described in this report.

North Dakota, South Dakota, Montana, Wyoming

SWToolbox: A surface-water tool-box for statistical analysis of streamflow time series

This report is a user guide for the low-flow analysis methods provided with version 1.0 of the Surface Water Toolbox (SWToolbox) computer program. The software combines functionality from two software programs—U.S. Geological Survey (USGS) SWSTAT and U.S. Environmental Protection Agency (EPA) DFLOW. Both of these programs have been used primarily for computation of critical low-flow statistics. The main analysis methods are the computation of hydrologic frequency statistics such as the 7-day minimum flow that occurs on average only once every 10 years (7Q10), computation of design flows including biologically based flows, and computation of flow-duration curves and duration hydrographs. Other annual, monthly, and seasonal statistics can also be computed. The interface facilitates retrieval of streamflow discharge data from the USGS National Water Information System and outputs text reports for a record of the analysis. Tools for graphing data and screening tests are available to assist the analyst in conducting the analysis.

Techniques and Methods

Mercury in U.S. coal—Priorities for new U.S. Geological Survey studies

In 2011, the U.S. Environmental Protection Agency (EPA) introduced emissions standards, known as Mercury and Air Toxics Standards (MATS), for a range of toxic constituents from coal-fired utility power stations and other combustion sources. This report presents the findings of an expert panel convened in September 2014 to assess the role of the U.S. Geological Survey (USGS) in new coal investigations that would be useful to stakeholders under MATS. Panel input is provided as summaries of responses to a questionnaire distributed to participants. The panel suggests that the USGS continue its work on trace elements in coal and include more information about delivered coals and boiler feed coals, in comparison to previous USGS compilations that emphasized sampling representative of coals in the ground. To be useful under multipollutant regulatory standards, investigation of a range of constituents in addition to mercury would be necessary. These include other toxic metals proposed for regulation, such as arsenic, nickel, cadmium, and chromium, as well as the halogens chlorine and fluorine, which upon emission form harmful acid gases. Halogen determinations are also important because they influence mercury speciation in flue gas, which allows the effectiveness of mercury controls to be assessed and predicted. The panel suggests that the Illinois Basin and the Powder River Basin should have the highest priority for new coal quality investigations in the near term by the USGS, on the basis of current economic conditions and overall economic importance, respectively. As a starting point for new investigations, brief summaries of the distribution of mercury in each coal basin, and their potential for further investigation, are presented.

Open-File Report

Loch Vale Watershed Project quality assurance report, 1995-1998

The Loch Vale Watershed (LVWS) project was initiated in 1980 by the National Park Service with funding from the Aquatic Effects Research Program of the National Acid Precipitation Assessment Program. Initial research objectives were to understand the processes that would either mitigate or accelerate the effects of pollution on soil and surface water chemistry, and to build a record in which long-term trends could be identified and examined. It is important for all data collected in Loch Vale to meet the high standards of quality set forth in previous LVWS QA/QC reports and LVWS Methods Manuals. Given the ever-widening usage of data collected in Loch Vale, it is equally important to provide users of that data with a report assuring that all data are sound. Parameters covered in this report are the quality of meteorological measurements, hydrological measurements, surface water chemistry, and similarities in catch efficiency of two raingage types in Loch Vale for the period of 1995-1998. Routine sampling of weather conditions, precipitation chemistry, and stream/lake water chemistry began in 1982. Since then, all samples and data have been analyzed according to widely accepted and published methods. Weather data have been collected, analyzed, and stored by LVWS project personnel. Methods for the handling of meteorological data are well documented (Denning 1988, Edwards 1991, Newkirk 1995,and Allstott 1995). Precipitation chemistry has always been collected according to National Atmospheric Deposition Program protocol (Bigelow 1988), and analyzed at the Central Analytical Laboratory of the Illinois State Water Survey in Champaign, IL. QA/QC procedures of the National Atmospheric Deposition Program are well documented (Aubertin 1990). Protocols for sampling surface waters are also well documented (Newkirk 1995). Analysis of surface water chemistry has been performed using standard EPA protocol at the US Forest Service's Rocky Mt. Station Biogeochemistry Laboratory since 1993.

Open-File Report

Baseline environmental monitoring of groundwater, surface water, and soil at the Ammonium Perchlorate Rocket Motor Destruction Facility at the Letterkenny Army Depot, Chambersburg, Pennsylvania, 2016

Letterkenny Army Depot in Chambersburg, Pennsylvania, built an Ammonium Perchlorate Rocket Motor Destruction (ARMD) facility in 2016. The ARMD Facility was designed to centralize rocket motor destruction and contain or capture all waste during the destruction process. Ideally, there would be no contaminant transport to air, soil, or water from the facility, but the Code of Federal Regulations requires that any hazardous waste disposal facility have an environmental monitoring program in place. In a study by the U.S. Geological Survey, in cooperation with the Letterkenny Army Depot, baseline characterization of constituents in groundwater, surface water, and soil was conducted from September to December 2016 to document site conditions prior to the beginning of operations at the facility in January 2017. Groundwater wells, surface water, and soils were sampled monthly during the baseline characterization period. No sediment transport from the site occurred on days when samples were collected from surface-water sites, so no sediment was collected from the retention basin at the facility during the baseline period. Data collected during the baseline period can be compared to data collected in future years to determine whether there is any contaminant transport from the ARMD Facility to the surrounding environment. During the baseline characterization period, monthly samples were collected from 4 groundwater wells and 9 soil sites near the ARMD Facility. The only surface-water site sampled monthly during the baseline period was upgradient from the facility. There was no streamflow at surface-water sites downgradient from the facility on days when surface-water samples were collected during the baseline characterization period. Groundwater results for the four wells sampled near the ARMD Facility during the baseline period did not show any major water-quality issues. Mean specific conductance (SC) and pH in groundwater ranged from 220 to 771 microsiemens per centimeter at 25 degrees Celsius (μS/cm) and 6.45 to 6.98, respectively. No constituents in groundwater samples exceeded any U.S. Environmental Protection Agency (EPA) Maximum Contaminant Level (MCL). Dissolved iron (Fe) was the only groundwater constituent that exceeded a Secondary Maximum Contaminant Level (SMCL) established by the EPA. The SMCL for Fe is 300 micrograms per liter (μg/L); samples from three wells had mean dissolved Fe concentrations ranging from 1,100 to 2,600 μg/L. The only volatile organic compounds (VOCs) detected in groundwater samples were bromomethane, acetone, and chloromethane. All VOC detections in groundwater samples were less than the Reporting Detection Levels (RDLs). These three compounds also were detected in blank samples submitted for groundwater samples. Perchlorate was not detected in any groundwater sample collected during the baseline period. Surface-water data collected during the baseline period were strictly representative of a stream reach upgradient from the ARMD Facility. Stream discharge ranged from 0.03 to 0.08 cubic feet per second during sample collection. The mean SC and pH were 310 μS/cm and 7.6, respectively. No EPA established MCLs or SMCLs were exceeded for any constituents in samples collected from this upgradient stream. Some VOCs were detected in surface water at less than the RDLs. The VOCs detected in surface water were generally the same VOCs as those detected at less than the RDLs for groundwater. Perchlorate was detected in each sample collected from the stream; the mean concentration was 0.07 μg/L. All perchlorate results were less than the RDL of 0.2 μg/L. Soil samples collected during the baseline period did not have any constituent concentrations that exceeded any medium-specific concentrations (MSC) or soil screening levels (SSL) established by either the Commonwealth of Pennsylvania or the EPA. The Commonwealth of Pennsylvania calculates MSCs based on either a function of acceptable concentrations in groundwater or based on health concerns if the soil is directly contacted. The EPA derives acceptable concentrations of constituents (SSLs) in soil based on standardized equations combining exposure information assumptions with EPA toxicity data. The EPA calculates SSLs for residential and industrial sites. Soil sites at the ARMD Facility were considered “industrial” for comparative purposes. There was at least one order of magnitude difference between any inorganic constituent concentration detected in soil and the MSC and (or) SSL for that constituent. Four VOCs were detected in soil samples collected during the baseline period. None of the VOCs detected in the soils were within three orders of magnitude of any established MSCs or SSLs. The VOCs detected in soil were dichloromethane (also known as methylene chloride), methyl tert-butyl ether (MTBE), tetrachloroethene, and acetone (only detected once). Dichloromethane was the only VOC detected at greater than the RDLs; concentrations in all soil samples were greater than the RDLs. Dichloromethane concentrations ranged from 1.9 to 50.1 micrograms per kilogram (μg/kg). MTBE was detected in 50 percent of samples collected but all results were less than the RDLs of 1.7 to 2.6 μg/kg. Tetrachloroethene was detected in 20 percent of soil samples collected, with a maximum estimated value of 1.5 μg/kg. Inorganic constituents with the highest concentrations in soil were Fe and aluminum (Al); mean Fe and Al concentrations ranged from 28,700 to 52,400 and 10,300 to 19,800 milligrams per kilogram (mg/kg), respectively. Data collected during the baseline period in 2016 can be compared to future data to determine whether concentrations in water and soils surrounding the facility have shown any changes that could be caused by the facility operation.

Pennsylvania

Water resources of Spink County, South Dakota

Spink County, an agricultural area of about 1,505 square miles, is in the flat to gently rolling James River lowland of east-central South Dakota. The water resources are characterized by the highly variable flows of the James River and its tributaries and by aquifers both in glacial deposits of sand and gravel, and in sandstone in the bedrock. Glacial aquifers underlie about half of the county, and bedrock aquifers underlie most of the county. The James River is an intermittent prairie stream that drains nearly 8,900 square miles north of Spink County and has an average annual discharge of about 124 cubic feet per second where it enters the county. The discharge is augmented by the flow of Snake and Turtle Creeks, each of which has an average annual flow of about 25 to 30 cubic feet per second. Streamflow is unreliable as a water supply because precipitation, which averages 18.5 inches annually, is erratic both in volume and in distribution, and because the average annual potential evapotranspiration rate is 43 inches. The flow of tributaries generally ceases by summer, and zero flows are common in the James River in fall and winter. Aquifers in glacial drift deposits store nearly 3.3 million acre-feet of fresh to slightly saline water at depths of from near land surface to more than 500 feet below land surface beneath an area of about 760 square miles. Yields of properly developed wells in the more productive aquifers exceed 1,000 gallons per minute in some areas. Withdrawals from the aquifers, mostly for irrigation, totaled about 15,000 acre-feet of water in 1990. Water levels in observation wells generally have declined less than 15 feet over several decades of increasing pumpage for irrigation, but locally have declined nearly 30 feet. Water levels generally rose during the wet period of 1983-86. In Spink County, bedrock aquifers store more than 40 million acre-feet of slightly to moderately saline water at depths of from 80 to about 1,300 feet below land surface. Yields of properly developed wells range from 2 to 600 gallons per minute. The artesian head of the heavily used Dakota aquifer has declined about 350 feet in the approximately 100 years since the first artesian wells were drilled in the county, but water levels have stabilized locally as a result of decreases in the discharge of water from the wells. Initial flows of from 4 gallons per minute to as much as 30 gallons per minute of very hard water can be obtained in the southwestern part of the county, where drillers report artesian heads of nearly 100 feet above land surface. The quality of water from aquifers in glacial drift varies greatly, even within an aquifer. Concentrations of dissolved solids in samples ranged from 151 to 9,610 milligrams per liter, and hardness ranged from 84 to 3,700 milligrams per liter. Median concentrations of dissolved solids, sulfate, iron, and manganese in some glacial aquifers are near or exceed Secondary Maximum Contaminant Levels (SMCL's) established by the U.S. Environmental Protection Agency (EPA). Some of the water from aquifers in glacial drift is suitable for irrigation use. Water samples from aquifers in the bedrock contained concentrations of dissolved solids that ranged from 1,410 to 2,670 milligrams per liter (sum of constituents) and hardness that ranged from 10 to 1,400 milligrams per liter; these concentrations generally are largest for aquifers below the Dakota aquifer. Median concentrations of dissolved solids, sulfate, iron, and manganese in Dakota wells either are near or exceed EPA SMCL's. Dissolved solids, sodium, and boron concentrations in water from bedrock aquifers commonly are too large for the water to be suitable for irrigation use.

Water-Resources Investigations Report

Occurrence and distribution of arsenic and radon in water from private wells in the Rancocas aquifer, southern New Castle and northern Kent Counties, Delaware, 2015

Water samples were collected and analyzed for arsenic and radon from 36 private, mostly domestic wells that tap the Rancocas aquifer in southern New Castle and northern Kent Counties, Delaware, during the summer of 2015. Both arsenic and radon are from natural mineral sources, in particular glauconitic and other marine-derived sediments, which are important components of the geologic formations comprising the Rancocas aquifer. Routine testing of domestic wells is not required in Delaware; as a result, many homeowners are not aware of potential water-quality problems with these chemicals in their well water. Arsenic has previously been detected at levels of potential concern for human health in this aquifer in adjacent parts of Maryland where it is referred to as the Aquia aquifer. Arsenic and radon also have previously been detected in several Rancocas aquifer wells in Delaware. The Delaware Department of Natural Resources and Environmental Control intends to use the data from this project to better identify areas with potential for levels of concern for domestic well owners. This report includes chemical results and maps showing the distribution of sampled wells and concentrations of arsenic and radon. All data collected for this study also are available in the U.S. Geological Survey’s National Water Information System database. Arsenic was detected above the minimum reporting limit of 0.1 micrograms per liter (µg/L) in 34 of the 36 wells sampled with concentrations ranging from about 0.11 to 27 µg/L. In 15 of the samples, arsenic concentrations were at or above the U.S. Environmental Protection Agency (EPA) Maximum Contaminant Level (MCL) of 10 µg/L for public wells. Most of the higher concentrations are clustered along a band running from the southwest to northeast in the southern part of the study area. Radon, which is an inert gas derived from radium, was detected in all water samples with concentrations ranging from 85 to 1,870 picocuries per liter (pCi/L). Currently, the EPA has not set a MCL for radon in public water systems. There were no samples where radon was detected at a concentration exceeding the proposed alternative MCL of 4,000 pCi/L. Samples from 16 of 36 wells were above the lower proposed MCL of 300 pCi/L. Most of these samples were from wells greater than 200 feet deep located in a similar part of the aquifer as the higher concentrations of arsenic along an east-northeasterly line in the southern part of the study area.

Delaware

Land-Cover Trends of the Southern California Mountains Ecoregion

This report presents an assessment of land-use and land-cover (LU/LC) change in the Southern California Mountains ecoregion for the period 1973-2001. The Southern California Mountains is one of 84 Level-III ecoregions as defined by the U.S. Environmental Protection Agency (EPA). Ecoregions have served as a spatial framework for environmental resource management, denoting areas that contain a geographically distinct assemblage of biotic and abiotic phenomena including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The established Land Cover Trends methodology generates estimates of change for ecoregions using a probability sampling approach and change-detection analysis of thematic land-cover images derived from Landsat satellite imagery.

Scientific Investigations Report