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Mapping elemental contamination on Palmyra Atoll National Wildlife Refuge

Palmyra Atoll, once a WWII U.S. Navy air station, is now a U.S. National Wildlife Refuge with nearly 50 km 2 of coral reef and 275 ha of emergent lands with forests of Pisonia grandis trees and colonies of several bird species. Due to the known elemental and organic contamination from chemicals associated with aviation, power generation and transmission, waste management, and other air station activities, a screening survey to map elemental concentrations was conducted. A map of 1944 Navy facilities was georeferenced and identifiable features were digitized. These data informed a targeted survey of 25 elements in soils and sediment at locations known or suspected to be contaminated, using a hand-held X-ray fluorescence spectrometer. At dozens of locations, concentrations of elements exceeded established soil and marine sediment thresholds for adverse ecological effects. Results were compiled into a publicly available geospatial dataset to inform potential remediation and habitat restoration activities.

Marine Pollution Bulletin↗

Environmental Assessment of the Muscatatuck Urban Training Center near Butlerville, Indiana, October and November 2005

An environmental assessment of the Muscatatuck Urban Training Center near Butlerville in Jennings County, Indiana, was completed during October and November 2005. As part of the Department of Defense Earth Science Program, the U.S. Geological Survey collected information about environmental conditions at the 825-acre former State of Indiana mental health facility prior to its conversion by the Indiana National Guard into an urban training center. The assessment was designed to investigate the type and extent of potential contamination associated with historical activities in selected areas of the facility. Samples of surface water, ground water, surface soil, and buried sediment were collected for the assessment in seven geographic study areas. Surface-water samples were collected from flowing and pooled surface water, as well as seeps and springs where ground water discharged at the land surface. Ground-water samples were collected from temporary wells installed in boreholes drilled to bedrock. Surface-soil samples were collected near sites of possible contamination. Buried-sediment samples were taken from core material collected near the top of bedrock at depths of 6.4 to 26 feet. For the assessment, 59 environmental, 22 quality-assurance, and 46 laboratory-blank samples were analyzed for as many as 65 volatile organic compounds, 62 semivolatile organic compounds, 20 trace elements, 10 inorganic cations and anions, 3 nutrients, and 4 water-quality characteristics. Concentrations of constituents detected in these samples were compared with regulatory standards (the Indiana Surface-Water-Quality Standards and Indiana Ground-Water-Quality Standards) and guidance criteria from the Indiana Department of Environmental Management's Risk Integrated System of Closures for contaminated soil and ground water. Standards or criteria were exceeded by 17 constituent concentrations in 11 environmental samples from 5 of the 7 geographic study areas. Standards or criteria were exceeded for 10 constituents: ammonia, arsenic, benzo(a)pyrene, beryllium, chloride, chloroform, copper, lead, sulfate, and zinc.

Indiana↗

Evaluation of available data on the geohydrology, soil chemistry, and ground-water chemistry of Gas Works Park and surrounding region, Seattle, Washington

Gas Works Park, in Seattle, Washington, is located at the site of an abandon gasification plant on Lake Union. Wastes deposited during 50 years of plant operations (1906-1956) have extended the shore line 100 ft and left the park soil contaminated with a number of hazardous material. Soil contaminants include polynuclear aromatic hydrocarbons (PAHs), polychlorinated biphenyls, pesticides, volatile organic compounds, cyanide, and metals. PAHs and metals have been detected in Lake Union sediments. Maximum total PAH concentrations exceeded 100 million micrograms/kilogram in some places in the soils of the park at 6-inch depths and in some lake sediments. Other contaminants present are much lower in concentrations. The park is on glacial drift overlain by gasification waste materials and clean fill. Waste materials include sand and gravels, mixed with lampblack, oil, bricks, and other industrial wastes. Groundwater flows through the soils and waste toward Lake Union. Vertical groundwater movement is uncertain, but is assumed to be upward near Lake Union. Concentrations of most soil contaminants are probably low in the groundwater and in Lake Union due to the low solubilities and high sorptive characteristics of these contaminants. However, no water quality data are available to confirm this premise. (USGS)

Water-Resources Investigations Report↗

Distribution of Cu, Co, As, and Fe in mine waste, sediment, soil, and water in and around mineral deposits and mines of the Idaho Cobalt Belt, USA

The distribution of Cu, Co, As and Fe was studied downstream from mines and deposits in the Idaho Cobalt Belt (ICB), the largest Co resource in the USA. To evaluate potential contamination in ecosystems in the ICB, mine waste, stream sediment, soil, and water were collected and analyzed for Cu, Co, As and Fe in this area. Concentrations of Cu in mine waste and stream sediment collected proximal to mines in the ICB ranged from 390 to 19,000 μg/g, exceeding the USEPA target clean-up level and the probable effect concentration (PEC) for Cu of 149 μg/g in sediment; PEC is the concentration above which harmful effects are likely in sediment dwelling organisms. In addition concentrations of Cu in mine runoff and stream water collected proximal to mines were highly elevated in the ICB and exceeded the USEPA chronic criterion for aquatic organisms of 6.3 μg/L (at a water hardness of 50 mg/L) and an LC50 concentration for rainbow trout of 14 μg/L for Cu in water. Concentrations of Co in mine waste and stream sediment collected proximal to mines varied from 14 to 7400 μg/g and were highly elevated above regional background concentrations, and generally exceeded the USEPA target clean-up level of 80 μg/g for Co in sediment. Concentrations of Co in water were as high as in 75,000 μg/L in the ICB, exceeding an LC50 of 346 μg/L for rainbow trout for Co in water by as much as two orders of magnitude, likely indicating an adverse effect on trout. Mine waste and stream sediment collected in the ICB also contained highly elevated As concentrations that varied from 26 to 17,000 μg/g, most of which exceeded the PEC of 33 μg/g and the USEPA target clean-up level of 35 μg/g for As in sediment. Conversely, most water samples had As concentrations that were below the 150 μg/L chronic criterion for protection of aquatic organisms and the USEPA target clean-up level of 14 μg/L. There is abundant Fe oxide in streams in the ICB and several samples of mine runoff and stream water exceeded the chronic criterion for protection of aquatic organisms of 1000 μg/L for Fe. There has been extensive remediation of mined areas in the ICB, but because some mine waste remaining in the area contains highly elevated Cu, Co, As and Fe, inhalation or ingestion of mine waste particulates may lead to human exposure to these elements.

Idaho↗

Evaluating soil contamination

This compilation was designed to help U.S. Fish and Wildlife Service contaminant specialists evaluate the degree of contamination of a soil, based on chemical analyses. Included are regulatory criteria, opinions, brief descriptions of scientific articles, and miscellaneous information that might be useful in making risk assessments. The intent was to make hard-to-obtain material readily available to contaminant specialists, but not to critique the material or develop new criteria. The compilation is to be used with its index, which includes about 200 contaminants. There are several entries for a few of the most thoroughly studied contaminants, but for most of them the information available is meager. Entries include soil contaminant criteria from other countries, contaminant guidelines for applying sewage sludge to soil, guidelines for evaluating sediments, background soil concentrations for various elements, citations to scientific articles that may help estimate the potential movement of soil contaminants into wildlife food chains, and a few odds and ends. Articles on earthworms were emphasized because they are a natural bridge between soil and many species of wildlife.

Biological Report↗

Coal-tar-based pavement sealcoat and PAHs: implications for the environment, human health, and stormwater management

Coal-tar-based sealcoat products, widely used in the central and eastern U.S. on parking lots, driveways, and even playgrounds, are typically 20−35% coal-tar pitch, a known human carcinogen that contains about 200 polycyclic aromatic hydrocarbon (PAH) compounds. Research continues to identify environmental compartments—including stormwater runoff, lake sediment, soil, house dust, and most recently, air—contaminated by PAHs from coal-tar-based sealcoat and to demonstrate potential risks to biological communities and human health. In many cases, the levels of contamination associated with sealed pavement are striking relative to levels near unsealed pavement: PAH concentrations in air over pavement with freshly applied coal-tar-based sealcoat, for example, were hundreds to thousands of times higher than those in air over unsealed pavement. Even a small amount of sealcoated pavement can be the dominant source of PAHs to sediment in stormwater-retention ponds; proper disposal of such PAH-contaminated sediment can be extremely costly. Several local governments, the District of Columbia, and the State of Washington have banned use of these products, and several national and regional hardware and home-improvement retailers have voluntarily ceased selling them.

Environmental Science & Technology↗

Anthropogenic vs. natural pollution: An environmental study of an industrial site under remediation (Naples, Italy)

Heavy metal concentrations and Pb isotopic composition were determined in the soils, slags, scums and landfill materials from a shut down industrial (brownfield) site. This was the second largest integrated steelworks in Italy, and is now under remediation by a Government project. It is located in the outskirts of Napoli on the Bagnoli-Fuorigrotta plain (BFP), which is part of the Campi Flegrei (CF) volcanic caldera, where many spas and geothermal springs occur. The purpose of this work is to distinguish the natural (geogenic) component, originated by hydrothermal activity, from anthropogenic contamination owing to industrial activity. 'In-situ sediments' (soils), slags, scums and landfill materials from 20 drill-cores were selected from a network of 197 drills carried out on a 100 ?? 100 m grid, covering the entire brownfield site. In general, heavy metal enrichments in the upper 3 m of the cores strongly suggest mixing between natural (geogenic) and anthropogenic components. Pb isotopic data are suggestive of three potential end members, and confirm the existence of a strong natural component in addition to contamination from anthropogenic activities. The slags, scums and landfill materials have been proved, through mineralogy and leachate experiments, to be geochemically stable; this shows that metal pollutants are not bio-available and, hence, do not pose a risk to future developments on this site. The natural contribution of hydrothermal fluids to soil pollution, in addition to the non-bio-availability of metal pollutants from industrial materials, indicate that heavy metal remediation of soils in this area would be of little use. Continuous discharge from mineralized hydrothermal solutions would cancel out any remediation effort.

Geochemistry: Exploration, Environment, Analysis↗

Contaminated-sediment database development and assessment in Boston Harbor

Bottom sediments have been regarded as memory banks for contaminant inputs to urban waterways. Bottom sediments accumulate by the addition of particles that enter the waterway from many sources (U.S. National Research Council, 1989). Sediments include solid contaminants, as well as contaminants from the water column that are adsorbed on organic matter or soil (rock) particles. Sediments from Boston Harbor and adjacent parts of Massachusetts Bay are now among the most intensively studied in the Nation in terms of chemical composition. Scientists at the U.S. Geological Survey (USGS), Woods Hole, Mass., undertook a pioneering effort to assemble a database from all available sources of information on chemicals in sediments of the Boston Harbor study area. The database was created to help understand the distribution of sediment contaminants and their sources, transport, and other processes and to support environmental management. The work involved collaboration with the U.S. Environmental Protection Agency (USEPA), the U.S. Army Corps of Engineers (USACOE), the Massachusetts Water Resources Authority, and other organizations. More than 100,000 sediment measurements from more than 3,000 samples were gleaned from 1,500 references. New approaches were developed to scientifically edit and validate data from heterogeneous sources. The compiled data included inorganic and organic chemical information and physical parameters like sediment texture (grain size), as well as documentation to minimize a userđs need to track down hard-to-find reports.

Massachusetts↗

Partition of nonpolar organic pollutants from water to soil and sediment organic matters

The partition coefficients (Koc) of carbon tetrachloride and 1,2-dichlorobenzene between normal soil/sediment organic matter and water have been determined for a large set of soils, bed sediments, and suspended solids from the United States and the People's Republic of China. The Koc values for both solutes are quite invariant either for the soils or for the bed sediments; the values on bed sediments are about twice those on soils. The similarity of Koc values between normal soils and between normal bed sediments suggests that natural organic matters in soils (or sediments) of different geographic origins exhibit comparable polarities and possibly comparable compositions. The results also suggest that the process that converts eroded soils into bed sediments brings about a change in the organic matter property. The difference between soil and sediment Koc values provides a basis for identifying the source of suspended solids in river waters. The very high Koc values observed for some special soils and sediments are diagnostic of severe anthropogenic contamination.

Environmental Science & Technology↗

Pesticide residues in Hemlock and Canadice Lakes and their tributaries in western New York, 1997-98

In 1997, the U.S.Geological Survey (USGS) and the City of Rochester began a cooperative program to study the presence of pesticides (herbicides and insecticides) that occur at trace levels in Hemlock and Canadice Lakes and their tributaries. The most frequently detected pesticides in streamflow and lake-water samples were herbicides commonly used in agriculture — atrazine, metolachlor, and simazine. None of the concentrations of these compounds in the samples exceeded Federal or State water-quality standards. Differences in the concentrations among stream samples can be attributed to land use and streamflow, and the timing of rainfall in relation to herbicide application. The north (lower) end of Hemlock Lake can receive pesticides in agricultural runoff from northern parts of its watershed and Canadice Creek. These pesticide inputs bypass most of the lake and could periodically affect the water quality periodically affect the water quality at the City of Rochester intake. Pesticide concentrations in samples from the intake during this study, however, were about 100 times less than current Federal and State standards for drinking water. Residues of DDT, dieldrin, and mirex are present in low concentrations in the bottom sediments of both lakes, but none were detected in water samples. The use of these insecticides was banned in 1972,and their persistence in the lakebed sediments is probably due to erosion of contaminated soils from agricultural lands.

New York↗

Grass buffers for playas in agricultural landscapes: A literature synthesis

We summarize current knowledge about grass buffers for protecting small, isolated wetlands in agricultural contexts, including information relevant to protecting playas from runoff containing sediments, nutrients, pesticides, and other contaminants, and information on how buffers may affect densities and productivity of grassland birds. Land-uses surrounding the approximately 60,000 playas within the Playa Lakes Region (PLR), including intensive agriculture, feedlots, and oil extraction, can contribute to severe degradation of playas. Farming and grazing can lead to significant sedimentation in nearby playas, eliminating their ability to hold water, support the region’s biodiversity, or adequately recharge aquifers. Contaminants further degrade habitats and threaten the water quality of underlying aquifers, including the Ogallala Aquifer. Grass buffers hold promise as a management tool to reduce the amount of sediments and contaminants from agricultural runoff that enters playas. Effective buffer width is determined by acceptable sediment-reduction levels, potential water flow and velocity, landscape and soil variables, buffer species, and vegetation structure. Various models have been developed to predict buffer effectiveness; however, most of these models, including those provided by the Natural Resource Conservation Service (NRCS), remain unvalidated. The majority of buffer-effectiveness literature is based on simulated conditions in experimental trays or plots; no published studies of buffer design or effectiveness specifically address playas. Nonetheless, some general patterns have emerged regarding buffer design/effectiveness. Buffers 10–60 m wide are generally considered adequate for trapping most sediments, although in some cases buffers need to be >200 m. The U.S. Fish and Wildlife Service Partners for Wildlife Program in the Southern High Plains recommend a buffer width of ~33 m planted with a diverse mix of native shortgrasses and mixed grasses as a starting point. Most dissolved contaminants, however, are removed from runoff only when they infiltrate the soil, where microbes or other processes can break down or sequester contaminants. Promoting runoff infiltration requires wider buffers with denser stem densities than those required for filtering sediments, which may result in hydrological changes in playas. Ultimately, the balance between runoff and infiltration determines whether or not water eventually reaches a given basin. Long-term buffer effectiveness requires regular maintenance, including excavation to remove overburdens of sediments, repairing vegetation damage, and removing over-mature vegetation or invasions of noxious weeds. Buffers may not be enough to protect playas; best management practices (BMPs; e.g., conservation tillage, contour tilling, and mulching herbicides into soil after application) that diminish soil erosion and contaminant runoff also may be necessary. Nutrient loads in runoff can be minimized by balancing nutrient input with nutrient requirements for livestock and crops. Pesticide application practices also require careful evaluation. Mowing or grazing rather than use of herbicides offer alternatives for suppressing invasive or undesirable plant species in buffers. Future research should entail multiple-scale approaches at regional, wetland-complex, and individual watershed scales. Information needs include direct measures of buffer effectiveness in ‘real-world’ systems, refinement and field tests of buffer-effectiveness models, how buffers may affect floral and faunal communities of playas, and basic ecological information on playa function and playa wildlife ecology. Understanding how wildlife communities respond to patch size and habitat fragmentation is crucial for addressing questions regarding habitat quality of grass buffers in playa systems.

Open-File Report↗

Mercury in the Sudbury River (Massachusetts, USA): pollution history and a synthesis of recent research

We review the transport, fate, and bioavailability of mercury in the Sudbury River, topics addressed in the following five papers. Mercury entered the river from an industrial complex (site) that operated from 1917 to 1978. Rates of mercury accumulation in sediment cores from two reservoirs just downstream from the site decreased soon after industrial operations ended and have decreased further since capping of contaminated soils at the site in 1991. The reservoirs contained the most contaminated sediments (some exceeding 50 mu g Hg.g dry weight(-1)) and were depositional sinks for total mercury. Methyl mercury concentrations in biota did not parallel concentrations of total mercury in the sediments to which organisms were exposed, experimentally or as residents. Contaminated wetlands within the floodplain about 25 km downstream from the site produced and exported methyl mercury from inorganic mercury that had originated from the site. Natural burial processes have gradually decreased the quantity of sedimentary mercury available for methylation within the reservoirs, whereas mercury in the lesser contaminated wetlands farther downstream has remained more available for transport, methylation, and entry into food webs.

Canadian Journal of Fisheries and Aquatic Sciences↗

Fish health study Ashtabula River natural resource damage assessment

INTRODUCTION The Ashtabula River is located in northeast Ohio, flowing into Lake Erie at Ashtabula, Ohio. Tributaries include Fields Brook, Hubbard Run, Strong Brook, and Ashtabula Creek. The bottom sediments, bank soils and biota of Fields Brook have been severely contaminated by unregulated discharges of hazardous substances. Hazardous substances have migrated downstream from Fields Brook to the Ashtabula River and Harbor, contaminating bottom sediments, fish and wildlife. There are presently more than 1,000,000 cubic yards of contaminated sediment in the Ashtabula River and Harbor, much of which originated from Fields Brook. Contaminants include polychlorinated biphenyls (PCBs), chlorinated benzenes, chlorinated ethenes, hexachlorobutadiene, polyaromatic hydrocarbons (PAHs), other organic chemicals, heavy metals and low level radionuclides. A Preassessment Screen, using existing data, was completed for the Ashtabula River and Harbor on May 18, 2001. Among the findings was that the fish community at Ashtabula contained approximately 45 percent fewer species and 52 percent fewer individuals than the Ohio EPA designated reference area, Conneaut Creek. The Ashtabula River and Conneaut Creek are similar in many respects, with the exception of the presence of contamination at Ashtabula. The difference in the fish communities between the two sites is believed to be at least partially a result of the hazardous substance contamination at Ashtabula. In order to investigate this matter further, the Trustees elected to conduct a study of the status and health of the aquatic biological communities of the Ashtabula River and Conneaut Creek in 2002-2004. The following document contains brief method descriptions (more detail available in attached Appendix A) and a summary of the data used to evaluate the health status of brown bullheads (Ameiurus nebulosus) and largemouth bass (Micropterus salmoides) collected from the above sites.

Ohio↗

Contaminant baselines and sediment provenance along the Puget Sound Energy Transport Corridor, 2015

The transport of coal and oil can result in contaminated soil, water, and organisms from unintended releases. Trains carrying coal and crude oil regularly pass through Puget Sound, Washington, and an increase in the number of coal and oil trains is expected in the future. This study characterized levels of potentially toxic contaminants in sediment in September 2015: arsenic, metals, and polycyclic aromatic hydrocarbons (PAHs) at four sites with fine-grained sediment (Chuckanut Bay, Padilla Bay, Snohomish River Delta, Nisqually River Delta) adjacent to the Burlington Northern Santa Fe (BNSF) rail line in the Puget Sound region. Arsenic (As) and metals levels were compared to those measured at a fifth site, urban Saltwater State Park, which was expected to show contaminants associated with urbanization but not rail transport of coal and oil because it is not adjacent to the BNSF rail line. Knowledge about current properties of soil and sediment is essential for quantifying impacts of spills and other releases, and for setting remediation or restoration targets. For the sampling effort and timing of this study, all five sites had fine sediment contents of cadmium (Cd), mercury (Hg), lead (Pb), and zinc (Zn) below minimal effects levels. Pb and Zn appeared to be urban sourced. Median As, chromium (Cr), copper (Cu), and nickel (Ni) levels were in the range where adverse biological effects would possibly occur; however, Cr and Ni were geologically sourced and unlikely to be bioavailable to organisms. As, Cu, and antimony (Sb) levels were highly correlated, an association that is characteristic of legacy smelting operations; however, total sediment contents of these three elements, along with Hg and As/Sb ratios, were near natural levels and could indicate river-borne inputs. Median total PAH concentrations were highest at Snohomish River Delta, but were below minimal effects levels at all sites. Diagnostic PAH ratios were indicative of PAHs sourced from petroleum combustion and coal/biomass burning, rather than from spilled petroleum or coal. Rare earth element patterns were distinct among watersheds with Cascade volcanoes, granitic rocks, or non-volcanic sediments, making them promising sediment provenance indicators. Knowledge about sediment sources and contaminant distributions could provide unique insights about sediment-bound contaminant sourcing, delivery, and dispersal in nearshore regions.

Washington↗

Assessment of mercury in sediments and waters of Grubers Grove Bay, Wisconsin

Mercury is a global contaminant that can be detrimental to wildlife and human health. Anthropogenic emissions and point sources are primarily responsible for elevated mercury concentrations in sediments and waters. Mercury can physically move and chemically transform in the environment, resulting in biomagnification of mercury, in the form of methylmercury, in the food web and causing elevated mercury concentrations in upper trophic levels. The ability to measure total mercury concentrations in the environment has existed for several decades and makes it possible to detect hotspots that might exist because of ongoing or previous anthropogenic activity. However, recent (within the past 15 years) developments in mass spectrometry have made it possible to complete low level stable isotope analysis allowing for the determination of mercury sources—natural and anthropogenic—in the environment through “fingerprinting.” Grubers Grove Bay in Lake Wisconsin, the focus area of this study, was determined to have elevated mercury levels even after multiple remediation efforts, resulting in its listing on the Federal list of impaired waters pursuant to the Clean Water Act. Adjacent to the bay is the former Badger Army Ammunition Plant, which manufactured ammunition for the U.S. Army during the early and middle 20th century, after which it was put on standby before being fully decommissioned. This study assesses mercury concentrations in the sediments and suspended particulate matter of Grubers Grove Bay, Wiegands Bay, and upstream sites, and in adjacent soils on the former Badger Army Ammunition Plant site. This study confirmed that mercury contamination exists in the sediments of Grubers Grove Bay even after dredging attempts by the U.S. Army. Additionally, using isotope ratios and a two-endmember mixing model, it was determined that soil from within Badger Army Ammunition Plant’s former site contributed a substantial amount of mercury to the bay. This result was supported by an observed gradient of high to low mercury concentrations from the innermost (nearest Badger Army Ammunition Plant) to the outermost (farthest from Badger Army Ammunition Plant) part of the bay.

Wisconsin↗

An overview of current applications, challenges, and future trends in distributed process-based models in hydrology

Process-based hydrological models have a long history dating back to the 1960s. Criticized by some as over-parameterized, overly complex, and difficult to use, a more nuanced view is that these tools are necessary in many situations and, in a certain class of problems, they are the most appropriate type of hydrological model. This is especially the case in situations where knowledge of flow paths or distributed state variables and/or preservation of physical constraints is important. Examples of this include: spatiotemporal variability of soil moisture, groundwater flow and runoff generation, sediment and contaminant transport, or when feedbacks among various Earth’s system processes or understanding the impacts of climate non-stationarity are of primary concern. These are situations where process-based models excel and other models are unverifiable. This article presents this pragmatic view in the context of existing literature to justify the approach where applicable and necessary. We review how improvements in data availability, computational resources and algorithms have made detailed hydrological simulations a reality. Avenues for the future of process-based hydrological models are presented suggesting their use as virtual laboratories, for design purposes, and with a powerful treatment of uncertainty.

Journal of Hydrology↗

Nitrogen species in soil, sediment, and ground water at a former sewage-treatment wastewater lagoon: Naval Air Station Whidbey Island, Island County, Washington

The potential for contamination of ground water from remnant sewage sludge in re-graded sediments of a deconstructed sewage-treatment lagoon was evaluated. Ground-water levels were measured in temporary drive-point wells, and ground-water samples were collected and analyzed for nutrients and other water-quality characteristics. Composite soil and sediment samples were collected and analyzed for organic carbon and nitrogen species. Multiple lines of evidence, including lack of appreciable organic matter in sediments of the former lagoon, agronomic analysis of nitrogen, the sequestration of nitrogen in the developing soils at the former lagoon, and likely occurrence of peat deposits within the aquifer material, suggest that the potential for substantial additions of nitrogen to ground water beneath the former sewage lagoon resulting from remnant sewage sludge not removed from the former lagoon are small. Concentrations of nitrogen species measured in ground-water samples were small and did not exceed the established U.S. Environmental Protection Agency’s maximum contaminant levels for nitrate (10 milligrams per liter). Concentrations of nitrate in ground-water samples were less than the laboratory reporting limit of 0.06 milligram per liter. Seventy to 90 percent of the total nitrogen present in ground water was in the ammonia form with a maximum concentration of 7.67 milligrams per liter. Concentrations of total nitrogen in ground water beneath the site, which is the sum of all forms of nitrogen including nitrate, nitrite, ammonia, and organic nitrogen, ranged from 1.15 to 8.44 milligrams per liter. Thus, even if all forms of nitrogen measured in ground water were converted to nitrate, the combined mass would be less than the maximum contaminant level. Oxidation-reduction conditions in ground water beneath the former sewage lagoon were reducing. Given the abundant supply of ambient organic carbon in the subsurface and in ground water at the former lagoon, any nitrate that may leach from residual sludge and be transported to ground water with recharge is expected to be quickly denitrified or transformed to nitrite and ammonia under the strongly reducing geochemical conditions that are present. Concentrations of organic carbon, the primary constituent of sewage sludge, in sediments of the former sewage lagoon were less than 1 percent, indicating a near absence of organic matter. The amount of total nitrogen present in the sediments at the former sewage lagoon was only about 25 percent of the amount typically present in developed agricultural soils. The lack of substantial carbon and nitrogen in sediments of the former sewage lagoon indicates that surficial sediments of the former lagoon are essentially devoid of residual sewage sludge. The largest concentration of total nitrogen measured in soil samples from the former sewage lagoon (330 milligrams per kilogram) was used to calculate an estimate of the amount of nitrogen that might be leached from residual sewage sludge by recharge. During the first two years following deconstruction of the former sewage lagoon, the concentration of total nitrogen in recharge leachate might exceed 10 milligrams per liter but the recharge leachate would not likely result in substantial increases in the nitrate concentration in ground water to concentrations greater than the drinking-water maximum contaminant level of 10 milligrams per liter.

Washington↗

Lead isotopic compositions of common arsenical pesticides used in New England

The three most important arsenical pesticides and herbicides that were extensively used on apple, blueberry, and potato crops in New England from mid-1800s to recent times are lead arsenate, calcium arsenate, and sodium arsenate. Lead arsenate was probably the most heavily used of the arsenical pesticides until it was banned in 1988. Other metal-arsenic pesticides were also used but in lesser amounts. A recent report identified areas in New England where arsenical pesticides were used extensively (Robinson and Ayuso, 2004). On the basis of factor analysis of metal concentrations in stream sediment samples, a positive correlation with pesticide use was shown in regions having stream sediment sample populations that contained concentrations of high arsenic and lead. Lead isotope compositions of stream sediments from areas with heavy use of the pesticides could not be entirely explained by lead originating from rock sulfides and their weathering products. An industrial lead contribution (mostly from atmospheric deposition of lead) was suggested in general to explain the lead isotopic distributions of the stream sediments that could not be accounted for by the natural lead in the environment. We concluded that when agricultural land previously contaminated with arsenical pesticides is urbanized, pesticide residues in the soils and stream sediments could be released into the groundwater. No lead isotopic data characterizing the compositions of pesticides were available for comparison. We have determined the lead isotopic compositions of commonly used pesticides in New England, such as lead arsenate, sodium metaarsenite, and calcium arsenate, in order to assist in future isotopic comparisons and to better establish anthropogenic sources of Pb and As. New data are also presented for copper acetoarsenite (or Paris green), methyl arsonic acid and methane arsonic acid, as well as for arsanilic acid, all of which are used as feed additives to promote swine and poultry growth. The new data characterize these anthropogenic sources. The data show that the arsenical pesticides have similar compositions: 208Pb/207Pb = 2.3839-2.4721, 206Pb/207Pb = 1.1035-1.2010, and 206Pb/204Pb = 17.070-18.759 and, more importantly, that the pesticides overlap the composition of the stream sediments that represent the areas with the most extensive agricultural use. Copper acetoarsenite (Paris green), arsenic oxide, methyl arsonic acid, methane arsonic acid, and arsanilic acid were also analyzed and have lead isotope compositions that range widely. An important source of arsenic and metals to most of the stream sediment samples in New England appears to be weathering products from rocks and industrial lead, but the extensive use of arsenical pesticides and herbicides up to about the 1960s can also be a significant anthropogenic source in agricultural regions.

Open-File Report↗