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USGS2009

Mercury Loads in the South River and Simulation of Mercury Total Maximum Daily Loads (TMDLs) for the South River, South Fork Shenandoah River, and Shenandoah River: Shenandoah Valley, Virginia

Due to elevated levels of methylmercury in fish, three streams in the Shenandoah Valley of Virginia have been placed on the State's 303d list of contaminated waters. These streams, the South River, the South Fork Shenandoah River, and parts of the Shenandoah River, are downstream from the city of Waynesboro, where mercury waste was discharged from 1929-1950 at an industrial site. To evaluate mercury contamination in fish, this total maximum daily load (TMDL) study was performed in a cooperative effort between the U.S. Geological Survey, the Virginia Department of Environmental Quality, and the U.S. Environmental Protection Agency. The investigation focused on the South River watershed, a headwater of the South Fork Shenandoah River, and extrapolated findings to the other affected downstream rivers. A numerical model of the watershed, based on Hydrological Simulation Program-FORTRAN (HSPF) software, was developed to simulate flows of water, sediment, and total mercury. Results from the investigation and numerical model indicate that contaminated flood-plain soils along the riverbank are the largest source of mercury to the river. Mercury associated with sediment accounts for 96 percent of the annual downstream mercury load (181 of 189 kilograms per year) at the mouth of the South River. Atmospherically deposited mercury contributes a smaller load (less than 1 percent) as do point sources, including current discharge from the historic industrial source area. In order to determine how reductions of mercury loading to the stream could reduce methylmercury concentrations in fish tissue below the U.S. Environmental Protection Agency criterion of 0.3 milligrams per kilogram, multiple scenarios were simulated. Bioaccumulation of mercury was expressed with a site-specific exponential relation between aqueous total mercury and methylmercury in smallmouth bass, the indicator fish species. Simulations indicate that if mercury loading were to decrease by 98.9 percent from 189 to 2 kilograms per year, fish tissue methylmercury concentrations would drop below 0.3 milligrams per kilogram. Based on the simulations, the estimated maximum load of total mercury that can enter the South River without causing fish tissue methylmercury concentrations to rise above 0.3 milligrams per kilogram is 2.03 kilograms per year for the South River, and 4.12 and 6.06 kilograms per year for the South Fork Shenandoah River and Shenandoah River, respectively.

Scientific Investigations Report↗

USGS1997

Phytotoxicity of floodplain soils contaminated with trace metals along the clark fork river, Grant-Kohrs Ranch National Historic Site, Deer Lodge, Montana, United States

Concentrations of metals in sediments and soils deposited along the floodplain of the Clark Fork River, within the Grant-Kohrs Ranch National Historic Site, Deer Lodge, Montana, USA, have exceeded maximum background concentrations in the United States for most metals tested. As a result of mining and smelting activities, portions of the Deer Lodge Valley, including the Grant-Kohrs Ranch, have received National Priority List Designation under the Comprehensive Environmental Response, Compensation and Liability Act. Using a series of plant germination tests, pH measurements, and metal analyses, this study investigated the toxicity of soils from floodplain 'slicken' areas, bare spots devoid of vegetation, along the Clark Fork River. The slicken soils collected from the Grant-Kohrs Ranch were toxic to all four plant species tested. The most sensitive endpoint in the germination tests was root length and the least sensitive was emergence. Considering emergence, the most sensitive species was the resident grass species Agrostis gigantea. The sensitivities were reversed when root lengths were examined, with Echinochloa crusgalli showing the greatest sensitivity. Both elevated concentrations of metals and low pH were necessary to produce an acutely phytotoxic response in laboratory seed germination tests using slicken soils. Moreover, pH values on the Grant-Kohrs Ranch appear to be a better predictor of acutely phytotoxic conditions than total metal levels.

Environmental Toxicology and Chemistry↗

USGS2008

Reducing sedimentation of depressional wetlands in agricultural landscapes

Depressional wetlands in agricultural landscapes are easily degraded by sediments and contaminants accumulated from their watersheds. Several best management practices can reduce transport of sediments into wetlands, including the establishment of vegetative buffers. We summarize the sources, transport dynamics, and effect of sediments, nutrients, and contaminants that threaten wetlands and the current knowledge of design and usefulness of grass buffers for protecting isolated wetlands. Buffer effectiveness is dependent on several factors, including vegetation structure, buffer width, attributes of the surrounding watershed (i.e., area, vegetative cover, slope and topography, soil type and structure, soil moisture, amount of herbicides and pesticides applied), and intensity and duration of rain events. To reduce dissolved contaminants from runoff, the water must infiltrate the soil where microbes or other processes can break down or sequester contaminants. But increasing infiltration also diminishes total water volume entering a wetland, which presents threats to wetland hydrology in semi-arid regions. Buffer effectiveness may be enhanced significantly by implementing other best management practices (e.g., conservation tillage, balancing input with nutrient requirements for livestock and crops, precision application of chemicals) in the surrounding watershed to diminish soil erosion and associated contaminant runoff. Buffers require regular maintenance to remove sediment build-up and replace damaged or over-mature vegetation. Further research is needed to establish guidelines for effective buffer width and structure, and such efforts should entail a coordinated, regional, multi-scale, multidisciplinary approach to evaluate buffer effectiveness and impacts. Direct measures in "real-world" systems and field validations of buffer-effectiveness models are crucial next steps in evaluating how grass buffers will impact the abiotic and biotic variables attributes that characterize small, isolated wetlands. ?? 2008 The Society of Wetland Scientists.

Wetlands↗

USGS2000

Stratigraphy and historic accumulation of mercury in recent depositional sediments in the Sudbury River, Massachusetts, USA

The distribution and deposition of sedimentary mercury in the Sudbury River were linked to an industrial complex (Nyanza site) that operated from 1917 through 1978. In two reservoirs just downstream from the Nyanza site, estimated rates of mercury accumulation increased markedly in the 1920s and 1930s, were greatest during 1976-1982, decreased within 5 years after industrial operations ceased, and have decreased further since capping of contaminated soil at the Nyanza site was completed in 1991. The most contaminated sediments were typically buried, yet the 0- to 1-cm stratum remained substantially contaminated in all cores. Mercury accumulating in the surficial, reservoir sediments was probably from continuing, albeit much lesser, inputs from the Nyanza site, whereas recent inputs to downstream wetland areas were attributed to recycling of sedimentary mercury or to mercury from unidentified local sources. In the reservoirs, burial of highly contaminated sediments is gradually decreasing the amount of sedimentary mercury available for methylation. In downstream wetlands, however, sedimentary mercury seemed to be more available than that in the reservoirs for physical transport and biogeochemical cycling.

Canadian Journal of Fisheries and Aquatic Sciences↗

USGS2014

Groundwater quality at Alabama Plating and Vincent Spring, Vincent, Alabama, 2007–2008

The former Alabama Plating site in Vincent, Alabama, includes the location where the Alabama Plating Company operated an electroplating facility from 1956 until 1986. The operation of the facility generated waste containing cyanide, arsenic, cadmium, chromium, copper, lead, zinc, and other heavy metals. Contamination resulting from the site operations was identified in groundwater, soil, and sediment. Vincent Spring, used as a public water supply by the city of Vincent, Alabama, is located about ½ mile southwest of the site. The U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, conducted an investigation at Vincent Spring and the Alabama Plating site, Vincent, Alabama, during 2007–2008 to evaluate the groundwater quality and evaluate the potential effect of contaminated groundwater on the water quality of Vincent Spring. The results of the investigation will provide scientific data and information on the occurrence, fate, and transport of contaminants in the water resources of the area and aid in the evaluation of the vulnerability of the public water supply to contamination. Samples were analyzed to evaluate the water quality at the former plating site, investigate the presence of possible contaminant indicators at Vincent Spring, and determine the usefulness of stable isotopes and geochemical properties in understanding groundwater flow and contaminant transport in the area. Samples collected from 16 monitor wells near the plating site and Vincent Spring were analyzed for major constituents, trace metals, nutrients, and the stable isotopes for hydrogen ( 2 H/H) and oxygen ( 18 O/ 16 O). Groundwater collected from Vincent Spring was characterized as a calcium-magnesium-bicarbonate water type with total dissolved solids concentrations ranging from 110 to 120 milligrams per liter and pH ranging from about 7.5 to 7.9 units. Groundwater chemistry at the monitor wells at the Alabama Plating site was highly variable by location and depth. Dissolved solids concentrations ranged from 28 to 2,880 milligrams per liter, and the water types varied from calcium-magnesium-bicarbonate-chloride, to calcium-sulfate or calcium-magnesium-sulfate, to sodium-chloride water types. The stable isotope ratios for hydrogen ( 2 H/H) and oxygen ( 18 O/ 16 O) for water from the monitor wells and from Vincent Spring, based on a single sampling event, can be separated into three groups: (1) Vincent Spring, (2) monitor wells MW03 and MW28, and (3) the remaining Alabama Plating monitor wells. The geochemical and stable isotope analyses indicate that water from Vincent Spring is distinct from water from the Alabama Plating monitor wells; however, this evaluation is based on a single sampling event. Although the water from Vincent Spring, for this sampling event, is different and does not seem to be affected by contaminated groundwater from the Alabama Plating site, additional hydrologic and water-quality data are needed to fully identify flow paths, the potential for contaminant transport, and water-quality changes through time.

Alabama↗

USGS1997

Assessing aquifer contamination risk using immunoassay: Trace analysis of atrazine in unsaturated zone sediments

The vulnerability of a shallow aquifer in south-central Kansas to contamination by atrazine (2-chloro-4-ethylamino-6-isopropylamines-triazine) was assessed by analyzing unsaturated zone soil and sediment samples from about 60 dryland and irrigated sites using an ultrasensitive immunoassay (detection level of 0.02 µg/kg) with verification by gas chromatography/mass spectrometry (GC/MS). Samples were collected at depths of 0 to 1.2 m (i.e., the root zone), 1.2 to 1.8 m, and 1.8 to 3.0 m during two time periods-prior to planting and after harvest of crops. About 75% of the samples contained detectable concentrations of parent atrazine. At the shallow sampling depth, atrazine concentrations ranged from 0.5 to approximately 12 µg/kg. Atrazine concentrations at the intermediate (1.2-1.8 m) depth generally were <1.0 µg/kg, with most of the concentrations <0.10 µg/kg, which suggests substantial degradation of parent atrazine in the root zone. Likewise, atrazine concentrations front the deepest (1.8-3.0 m) depth ranged from <0.02 to 0.33 µg/kg. The metabolite deethylatrazine (2-amino-4-chloro-6- isopropylamine-s-triazine) was detected by GC/MS only in 2 of 60 samples with concentrations of 1.4 and 1.5 µg/kg. The reconnaissance survey shows that, in spite of atrazine use ranging from 1 to 5 or more years, there does not appear to he a significant buildup of parent compound below the root zone. Therefore, the unsaturated zone does not appear to be a major storage compartment of atrazine contamination for the underlying shallow aquifer.

Journal of Environmental Quality↗

USGS2012

Concentration, distribution, and translocation of mercury and methylmercury in mine-waste, sediment, soil, water, and fish collected near the Abbadia San Salvatore mercury mine, Monte Amiata district, Italy

The distribution and translocation of mercury (Hg) was studied in the Paglia River ecosystem, located downstream from the inactive Abbadia San Salvatore mine (ASSM). The ASSM is part of the Monte Amiata Hg district, Southern Tuscany, Italy, which was one of the world’s largest Hg districts. Concentrations of Hg and methyl-Hg were determined in mine-waste calcine (retorted ore), sediment, water, soil, and freshwater fish collected from the ASSM and the downstream Paglia River. Concentrations of Hg in calcine samples ranged from 25 to 1500 μg/g, all of which exceeded the industrial soil contamination level for Hg of 5 μg/g used in Italy. Stream and lake sediment samples collected downstream from the ASSM ranged in Hg concentration from 0.26 to 15 μg/g, of which more than 50% exceeded the probable effect concentration for Hg of 1.06 μg/g, the concentration above which harmful effects are likely to be observed in sediment-dwelling organisms. Stream and lake sediment methyl-Hg concentrations showed a significant correlation with TOC indicating considerable methylation and potential bioavailability of Hg. Stream water contained Hg as high as 1400 ng/L, but only one water sample exceeded the 1000 ng/L drinking water Hg standard used in Italy. Concentrations of Hg were elevated in freshwater fish muscle samples and ranged from 0.16 to 1.2 μg/g (wet weight), averaged 0.84 μg/g, and 96% of these exceeded the 0.3 μg/g (methyl-Hg, wet weight) USEPA fish muscle standard recommended to protect human health. Analysis of fish muscle for methyl-Hg confirmed that > 90% of the Hg in these fish is methyl-Hg. Such highly elevated Hg concentrations in fish indicated active methylation, significant bioavailability, and uptake of Hg by fish in the Paglia River ecosystem. Methyl-Hg is highly toxic and the high Hg concentrations in these fish represent a potential pathway of Hg to the human food chain.

Monte Amiata↗

USGS1999

Hydroxyatrazine in soils and sediments

Hydroxyatrazine (HA) is the major metabolite of atrazine in most surface soils. Knowledge of HA sorption to soils, and its pattern of stream water contamination suggest that it is persistent in the environment. Soils with different atrazine use histories were collected from four sites, and sediments were collected from an agricultural watershed. Samples were exhaustively extracted with a mixed—mode extractant, and HA was quantitated using high performance liquid chromatography with UV detection. Atrazine, deethylatrazine (DEA), and deisopropylatrazine (DIA) were also measured in all samples. Concentrations of HA were considerably greater than concentrations of atrazine, DEA, and DIA in all soils and sediments studied. Soil concentrations of HA ranged from 14 to 640 μg/kg with a median concentration of 84 μg/kg. Sediment concentrations of HA ranged from 11 to 96 μg/kg, with a median concentration of 14 μg/kg. Correlations of HA and atrazine concentrations to soil properties indicated that HA levels in soils were controlled by sorption of atrazine. Because atrazine hydrolysis is known to be enhanced by sorption and pH extremes, soils with high organic matter (OM) and clay content and low pH will result in greater atrazine sorption and subsequent hydrolysis. Significant correlation of HA concentrations to OM, pH, and cation exchange capacity of sediments indicated that mixed—mode sorption (i.e., binding by cation exchange and hydrophobic interactions) was the mechanism controlling HA levels in sediment. The presence of HA in soils and stream sediments at the levels observed support existing hypotheses regarding its transport in surface runoff. These results also indicated that persistence of HA in terrestrial and aquatic ecosystems is an additional risk factor associated with atrazine usage.

Environmental Toxicology and Chemistry↗

USGS2018

Science support for evaluating natural recovery of polychlorinated biphenyl concentrations in fish from Crab Orchard Lake, Crab Orchard National Wildlife Refuge, Illinois

Introduction Crab Orchard Lake in southern Illinois is one of the largest and most popular recreational lakes in the state. Construction of the nearly 7,000-acre reservoir in the late 1930s created employment opportunities through the Works Progress Administration, and the lake itself was intended to supply water, control flooding, and provide recreational opportunities for local communities (Stall, 1954). In 1942, the Department of War appropriated or purchased more than 20,000 acres of land around Crab Orchard Lake and constructed the Illinois Ordnance Plant, which manufactured bombs and anti-tank mines during World War II. After the war, an Act of Congress transferred the property to the U.S. Department of the Interior. Crab Orchard National Wildlife Refuge was established on August 5, 1947, for the joint purposes of wildlife conservation, agriculture, recreation, and industry. Production of explosives continued, but new industries also moved onsite. More than 200 tenants have held leases with Crab Orchard National Wildlife Refuge and have operated a variety of manufacturing plants (electrical components, plated metal parts, ink, machined parts, painted products, and boats) on-site. Soils, water, and sediments in several areas of the refuge were contaminated with hazardous substances from handling and disposal methods that are no longer acceptable environmental practice (for example, direct discharge to surface water, use of unlined landfills). Polychlorinated biphenyl (PCB) contamination at the refuge was identified in the 1970s, and a PCB-based fish-consumption advisory has been in effect since 1988 for Crab Orchard Lake. The present advisory covers common carp ( Cyprinus carpio ) and channel catfish ( Ictalurus punctatus ); see Illinois Department of Public Health (2017). Some of the most contaminated areas of the refuge were actively remediated, and natural ecosystem recovery processes are expected to further reduce residual PCB concentrations in the lake. The U.S. Fish and Wildlife Service sought technical support to understand environmental drivers of current (2017) PCB residues in fish tissue and patterns in PCB residues through time to inform the fish-consumption advisory for Crab Orchard Lake. This project is planned in two phases (Tasks 1 and 2); the first phase is included in this report. Task 1, reported here, includes a review of existing literature and a brief overview focused on environmental and biochemical/physiological processes that drive PCB residues in fish tissue. This review specifically targets processes that are relevant for freshwater lacustrine environments such as those at Crab Orchard Lake. In addition to discussions of environmental fate, metabolism, and accumulation of PCBs, this review includes a brief scientifically based explanation of approaches used to establish fish-consumption advisories. A planned second task (Task 2) will include a compilation and summary of existing data on PCB residues in fish tissue samples from Crab Orchard Lake. This summary will also place Crab Orchard Lake data in a broader geographic context through a comparison with fish data from other Midwestern lakes. When Task 1 and Task 2 are complete, resource managers will have (a) a synthesis of existing literature that characterizes the processes influencing the fate of residual PCBs remaining in systems such as Crab Orchard Lake, (b) a summary of natural PCB attenuation processes for use in risk communication with the public, and (c) a summary of existing data on PCBs in fish tissues from Crab Orchard Lake, including exploratory plots of tissue residues through time. Overall, this project will provide data to help resource managers better understand the ecological and public health consequences of residual PCBs in Crab Orchard Lake.

Illinois↗

USGS2007

Investigation of ground-water contamination at a drainage ditch, Installation Restoration Site 4, Naval Air Station Corpus Christi, Corpus Christi, Texas, 2005–06

The U.S. Geological Survey, in cooperation with the Naval Facilities Engineering Command Southeast, used newly developed sampling methods to investigate ground-water contamination by chlorobenzenes beneath a drainage ditch on the southwestern side of Installation Restoration Site 4, Naval Air Station Corpus Christi, Corpus Christi, Texas, during 2005-06. The drainage ditch, which is a potential receptor for ground-water contaminants from Installation Restoration Site 4, intermittently discharges water to Corpus Christi Bay. This report uses data from a new type of pore-water sampler developed for this investigation and other methods to examine the subsurface contamination beneath the drainage ditch. Analysis of ground water from the samplers indicated that chlorobenzenes (maximum detected concentration of 160 micrograms per liter) are present in the ground water beneath the ditch. The concentrations of dissolved oxygen in the samples (less than 0.05-0.4 milligram per liter) showed that the ground water beneath and near the ditch is anaerobic, indicating that substantial chlorobenzene biodegradation in the aquifer beneath the ditch is unlikely. Probable alternative mechanisms of chlorobenzene removal in the ground water beneath the drainage ditch include sorption onto the organic-rich sediment and contaminant depletion by cattails through uptake, sorption, and localized soil aeration.

Texas↗

USGS2018

Tidal flushing of mercury from the Bremerton Naval Complex through the PSNS015 stormwater drain system to Sinclair Inlet, Kitsap County, Washington, 2011 -12

The sediments of Sinclair Inlet, in Puget Sound, Washington, have elevated levels of contaminants including mercury. The Bremerton Naval Complex is adjacent to Sinclair Inlet, and has known areas of historical soil mercury contamination. The U.S. Geological Survey, in cooperation with the U.S. Navy, has been investigating the potential for mercury sources on the Bremerton Naval Complex to recontaminate recently remediated marine sediment. In 2011–12, the U.S. Geological Survey conducted three tidal- related sampling campaigns to characterize mercury dynamics in the largest stormwater drain system on the Bremerton Naval Complex, which passes through the soils of an area known as Site 2 that has elevated soil mercury concentrations. The sampling campaigns confirmed that the stormwater drain system, PSNS015, serves as a conduit for seawater transport more than 250 m landward of the contaminated soils that subsequently facilitates mercury transport to Sinclair Inlet. During the December 2011 reconnaissance sampling campaign, no freshwater source of mercury to PSNS015 was identified. There was heavy precipitation preceding and stormwater runoff generated during the reconnaissance survey, which suggests that the primary source of mercury in PSNS015 is not precipitation-induced. During the May 2012 spring-tide sampling campaign, the water in PSNS015 drained to Sinclair Inlet during a negative low tide, and the highest filtered total mercury concentration in the stormwater drain system (60 ng/L) was measured during the lower-low tide in the freshwater flowing into the seaward-most stormwater drain vault from either up-pipe or local groundwater intrusion. Similar conditions were not observed during the June 2012 companion neap-tide sampling campaign, when the water-level elevation of the positive low tide in Sinclair Inlet dropped only slightly below the stormwater drain vault elevation, the water in the seaward-most stormwater vault was brackish rather than fresh, and the filtered total mercury concentration never exceeded 24 ng/L. Particulate total mercury concentrations and dynamics during the spring- and neap-tide sampling campaigns were variable, with higher concentrations (as much as 133 ng/L) measured throughout the neap-tide study compared to those measured during the spring-tide study (as much as 4.34 ng/L). The highest filtered total mercury concentration of all sampling campaigns (1,140 ng/L) was measured during ebb tide in a nearshore monitoring well that represents groundwater discharging from the contaminated soils directly to Sinclair Inlet along an unwalled part of the shoreline. The results suggest that mercury extracted from Site 2 soils can be carried to Sinclair Inlet during ebb tides by at least two mechanisms: (1) through groundwater directly to Sinclair Inlet along an unwalled part of the shoreline or (2) through the stormwater drain system when the water level in Sinclair Inlet drops below the water level in the stormwater drain system. The data can be used to guide future modifications to the seawall and stormwater drain system that aim to hydraulically disconnect the stormwater drain system from the surrounding contaminated soils.

Washington↗

USGS2013

Occurrence and variability of mining-related lead and zinc in the Spring River flood plain and tributary flood plains, Cherokee County, Kansas, 2009--11

Historical mining activity in the Tri-State Mining District (TSMD), located in parts of southeast Kansas, southwest Missouri, and northeast Oklahoma, has resulted in a substantial ongoing input of cadmium, lead, and zinc to the environment. To provide some of the information needed to support remediation efforts in the Cherokee County, Kansas, superfund site, a 4-year study was begun in 2009 by the U.S. Geological Survey that was requested and funded by the U.S. Environmental Protection Agency. A combination of surficial-soil sampling and coring was used to investigate the occurrence and variability of mining-related lead and zinc in the flood plains of the Spring River and several tributaries within the superfund site. Lead- and zinc-contaminated flood plains are a concern, in part, because they represent a long-term source of contamination to the fluvial environment. Lead and zinc contamination was assessed with reference to probable-effect concentrations (PECs), which represent the concentrations above which adverse aquatic biological effects are likely to occur. The general PECs for lead and zinc were 128 and 459 milligrams per kilogram, respectively. The TSMD-specific PECs for lead and zinc were 150 and 2,083 milligrams per kilogram, respectively. Typically, surficial soils in the Spring River flood plain had lead and zinc concentrations that were less than the general PECs. Lead and zinc concentrations in the surficial-soil samples were variable with distance downstream and with distance from the Spring River channel, and the largest lead and zinc concentrations usually were located near the channel. Lead and zinc concentrations larger than the general or TSMD-specific PECs, or both, were infrequent at depth in the Spring River flood plain. When present, such contamination typically was confined to the upper 2 feet of the core and frequently was confined to the upper 6 inches. Tributaries with few or no lead- and zinc-mined areas in the basin—Brush Creek, Cow Creek, and Shawnee Creek—generally had flood-plain lead and zinc concentrations (surficial soil, 6- and 12-inch depth) that were substantially less than the general PECs. Tributaries with extensive lead- and zinc-mined areas in the basin—Shoal Creek, Short Creek, Spring Branch, Tar Creek, Turkey Creek, and Willow Creek—had flood-plain lead concentrations (surficial soil, 6- and 12-inch depth) that frequently or typically exceeded the general and TSMD-specific PECs. Likewise, the tributaries with extensive lead- and zinc-mined areas in the basin had flood-plain zinc concentrations (surficial soil, 6- and 12-inch depth) that frequently or typically exceeded the general PEC. With the exception of Shoal and Willow Creeks, zinc concentrations typically exceeded the TSMD-specific PEC. The largest flood-plain lead and zinc concentrations (surficial soil, 6- and 12-inch depth) were measured for Short and Tar Creeks. Lead and zinc concentrations in the surficial-soil samples collected from the tributary flood plains varied longitudinally in relation to sources of mining-contaminated sediment in the basins. Lead and zinc concentrations also varied with distance from the channel; however, no consistent spatial trend was evident. For the surficial-soil samples collected from the Spring River flood plain and tributary flood plains, both the coarse (larger than 63 micrometers) and fine particles (less than 63 micrometers) contained substantial lead and zinc concentrations.

Kansas↗

USGS2011

Waste isolation and contaminant migration - Tools and techniques for monitoring the saturated zone-unsaturated zone-plant-atmosphere continuum

In 1976 the U.S. Geological Survey (USGS) began studies of unsaturated zone hydrology next to the Nation’s first commercial disposal facility for low-level radioactive waste (LLRW) near Beatty, NV. Recognizing the need for long-term data collection, the USGS in 1983 established research management areas in the vicinity of the waste-burial facility through agreements with the Bureau of Land Management and the State of Nevada. Within this framework, the Amargosa Desert Research Site (ADRS; http://nevada.usgs.gov/adrs/) is serving as a field laboratory for the sustained study of water-, gas-, and contaminant-transport processes, and the development of models and methods to characterize flow and transport. The research is built on multiple lines of data that include: micrometeorology; evapotranspiration; plant metrics; soil and sediment properties; unsaturated-zone moisture, temperature, and gas composition; geology and geophysics; and groundwater. Contaminant data include tritium, radiocarbon, volatile-organic compounds (VOCs), and elemental mercury. Presented here is a summary of monitoring tools and techniques that are being applied in studies of waste isolation and contaminant migration.

Conference Paper↗

USGS1996

Soil, water, and streambed quality at a demolished asphalt plant, Fort Bragg, North Carolina, 1992-94

A number of potentially hazardous chemicals were used at an asphalt plant on the Fort Bragg U.S. Army Reservation near Fayetteville, North Carolina. This plant was demolished in the late 1960's. Samples collected from soil, ground water, surface water, and streambed sediment were tested for the presence of contaminants. The sediment immediately underlying the demolished asphalt plant site consists mainly of sands, silts, and clayey sands with interbedded clay occurring at various depths. About 12 inches of rainfall per year infiltrate the unconfined surficial aquifer. The water table in this area is about 233 to 243 feet above sea level. Local ground water moves laterally, mainly towards the north- to-northwest at a rate of about 35 feet per year. where it discharges to Tank Creek, Little River, or one of their tributaries. A series of confining clays separate the surficial aquifer from the underlying upper Cape Fear aquifer. These clays help retard vertical migration of constituents dissolved in ground water. The saprolite-bedrock aquifer lies below the upper Cape Fear aquifer. In general ground water in the seven monitoring wells screened in the upper and lower part of the surficial aquifer did not contain detectable concentrations of chemicals related to past asphalt-plant activities. A small number of chemicals that were assumed to be unrelated to the asphalt plant were present in some of the study area monitoring wells. Ground water in four wells contained concentrations of organochlorine pesticides. Of these pesticides, concentrations of gamma-benzene hexachloride (lindane) (maximum of 0.76 micrograms per liter) exceeded the U.S. Environmental Protection Agency maximum contaminant level of 0.2 micrograms per liter in two wells. In addition, one well contained a trichloroethane concentration (7.7 micrograms per liter) that is assumed to be unrelated to demolished asphalt-plant operations, but exceeded the U.S. Environmental Protection Agency maximum contaminant level of 5.0 micrograms per liter. One well contained a fluoride concentration of 5.2 milligrams per liter that exceeded the U.S. Environmental Protection Agency maximum contaminant level of 4.0 milligrams per liter. Total and dissolved metals concentrations were generally typical of background levels. Some of the wells contained elevated levels of chloride (maximum of 749 milligrams per liter), specific conductance (maximum of 2,780 microsiemens per centimeter at 25 degrees Celsius), and dissolved solids (maximum of 1,520 milligrams per liter). Twelve of twenty-two soil samples that were collected at various depths at monitoring-well locations did not contain volatile organic compounds or polynuclear aromatic hydrocarbons. The remaining ten soil samples contained very low concentrations of polynuclear aromatic hydrocarbons and (or) analytical laboratory-related volatile organic compounds. The maximum concentrations were for fluoranthene and pyrene, at 780 and 750 micrograms per kilogram, respectively. In general, the polynuclear aromatic hydrocarbon concentrations were in sediment near the land surface. Streambed sediment from an unnamed, eastern tributary to Tank Creek in the eastern part of the site contained a small number of organochlorine pesticide compounds (a maximum of 1,400 milligrams per kilogram of 4,4'-DDD) and total petroleum hydrocarbons (113 milligrams per kilogram). Concentrations of metals and other inorganic constituents were generally typical of background concentrations. Surface water in this tributary did not contain elevated concentrations of anthropogenic chemicals.

North Carolina↗

USGS2023

Using mercury stable isotope fractionation to identify the contribution of historical mercury mining sources present in downstream water, sediment and fish

Ecosystems downstream of mercury (Hg) contaminated sites can be impacted by both localized releases as well as Hg deposited to the watershed from atmospheric transport. Identifying the source of Hg in water, sediment, and fish downstream of contaminated sites is important for determining the effectiveness of source-control remediation actions. This study uses measurements of Hg stable isotopes in soil, sediment, water, and fish to differentiate between Hg from an abandoned Hg mine from non-mine-related sources. The study site is located within the Willamette River watershed (Oregon, United States), which includes free-flowing river segments and a reservoir downstream of the mine. The concentrations of total-Hg (THg) in the reservoir fish were 4-fold higher than those further downstream (>90 km) from the mine site in free-flowing sections of the river. Mercury stable isotope fractionation analysis showed that the mine tailings (δ 202 Hg: −0.36‰ ± 0.03‰) had a distinctive isotopic composition compared to background soils (δ 202 Hg: −2.30‰ ± 0.25‰). Similar differences in isotopic composition were observed between stream water that flowed through the tailings (particulate bound δ 202 Hg: −0.58‰; dissolved: −0.91‰) versus a background stream (particle-bound δ 202 Hg: −2.36‰; dissolved: −2.09‰). Within the reservoir sediment, the Hg isotopic composition indicated that the proportion of the Hg related to mine-release increased with THg concentrations. However, in the fish samples the opposite trend was observed—the degree of mine-related Hg was lower in fish with the higher THg concentrations. While sediment concentrations clearly show the influence of the mine, the relationship in fish is more complicated due to differences in methylmercury (MeHg) formation and the foraging behavior of different fish species. The fish tissue δ 13 C and Δ 199 Hg values indicate that there is a higher influence of mine-sourced Hg in fish feeding in a more sediment-based food web and less so in planktonic and littoral-based food webs. Identifying the relative proportion of Hg from local contaminated site can help inform remediation decisions, especially when the relationship between total Hg concentrations and sources do not show similar covariation between abiotic and biotic media.

Oregon↗

USGS2019

Geochemical sourcing of runoff from a young volcanic watershed to an impacted coral reef in Pelekane Bay, Hawaii

Runoff of sediment and other contaminants from developed watersheds threatens coastal ecosystems and services. A sediment geochemical sourcing study was undertaken on a sediment-impacted coral reef flat to identify terrestrial sediment sources and how these changed over time. Geochemical signatures were identified for watershed soils that formed on Hawaiian basaltic and alkalic lavas using relatively immobile compatible (Ni, Sc) and incompatible (Nb, REE , Th) elements quantified by ICP-MS in total decompositions of the fine fraction of surface soils. Some soils also contained ash from late-erupting cinder cones that added alkalic geochemical signatures, resulting in distinctive mixed signatures near these geologic features. Sediment was collected in Pelekane Bay using sediment traps during winter 2010–2011 and a sediment core in order to geochemically source runoff entering the bay. Geochemical signatures in trapped sediment showed that runoff predominantly originated from the lower watershed along a highway corridor rather than from the upper watershed or areas with alkalic lavas. Soil in the highway corridor also contained Zn above levels of concern for aquatic organisms and anthropogenic Pb, indications that runoff control measures could reduce the exposure of the reef community to potentially toxic metals and other road-associated contaminants. The upper portion of a 60-yr long sediment record from Pelekane Bay was disturbed by tsunamigenic waves from the Tohoku earthquake , and the remainder was likely subject to mixing by winter waves that averaged out geochemical variations. On average, watershed regions with basaltic soils were the predominant source of runoff to the bay over the past 60 years. By linking sediment runoff to geographic regions or features in watersheds, geochemical sourcing can provide insights that allow resource managers to direct runoff mitigation and soil conservation efforts to areas where they will be most effective.

Hawaii↗

USGS2015

Levelling and merging of two discrete national-scale geochemical databases: A case study showing the surficial expression of metalliferous black shales

Government-sponsored, national-scale, soil and sediment geochemical databases are used to estimate regional and local background concentrations for environmental issues, identify possible anthropogenic contamination, estimate mineral endowment, explore for new mineral deposits, evaluate nutrient levels for agriculture, and establish concentration relationships with human or animal health. Because of these different uses, it is difficult for any single database to accommodate all the needs of each client. Smith et al. (2013, p. 168) reviewed six national-scale soil and sediment geochemical databases for the United States (U.S.) and, for each, evaluated “its appropriateness as a national-scale geochemical database and its usefulness for national-scale geochemical mapping.” Each of the evaluated databases has strengths and weaknesses that were listed in that review. Two of these U.S. national-scale geochemical databases are similar in their sample media and collection protocols but have different strengths—primarily sampling density and analytical consistency. This project was implemented to determine whether those databases could be merged to produce a combined dataset that could be used for mineral resource assessments. The utility of the merged database was tested to see whether mapped distributions could identify metalliferous black shales at a national scale.

Conference Paper↗

USGS2013

Assaying environmental nickel toxicity using model nematodes

Although nickel exposure results in allergic reactions, respiratory conditions, and cancer in humans and rodents, the ramifications of excess nickel in the environment for animal and human health remain largely undescribed. Nickel and other cationic metals travel through waterways and bind to soils and sediments. To evaluate the potential toxic effects of nickel at environmental contaminant levels (8.9-7,600 µg Ni/g dry weight of sediment and 50-800 µg NiCl 2 /L of water), we conducted assays using two cosmopolitan nematodes, Caenorhabditis elegans and Pristionchus pacificus . We assayed the effects of both sediment-bound and aqueous nickel upon animal growth, developmental survival, lifespan, and fecundity. Uncontaminated sediments were collected from sites in the Midwestern United States and spiked with a range of nickel concentrations. We found that nickel-spiked sediment substantially impairs both survival from larval to adult stages and adult longevity in a concentration-dependent manner. Further, while aqueous nickel showed no adverse effects on either survivorship or longevity, we observed a significant decrease in fecundity, indicating that aqueous nickel could have a negative impact on nematode physiology. Intriguingly, C. elegans and P. pacificus exhibit similar, but not identical, responses to nickel exposure. Moreover, P. pacificus could be tested successfully in sediments inhospitable to C. elegans . Our results add to a growing body of literature documenting the impact of nickel on animal physiology, and suggest that environmental toxicological studies could gain an advantage by widening their repertoire of nematode species.

PLoS ONE↗