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At least 37 records · Page 2Linked to original sources

Source and fate of inorganic soil contamination around the abandoned Phillips sulfide mine, hudson Highlands, New York

The abandoned Phillips sulfide mine in the critical Highlands watershed in New York has been shown to produce strongly acidic mine drainage (AMD) with anomalous metal contaminants in first-order streams that exceeded local water standards by up to several orders of magnitude (Gilchrist et al., 2009). The metal-sulfide-rich tailings also produce contaminated soils with pH < 4, organic matter < 2.5% and trace metals sequestered in soil oxides. A geochemical transect to test worst-case soil contamination showed that Cr, Co and Ni correlated positively with Mn, (r = 0.72, r= 0.89, r = 0.80, respectively), suggesting Mn-oxide sequestration and that Cu and Pb correlated with Fe (r = 0.76, r = 0.83, respectively), suggesting sequestration in goethite. Ubiquitous, yellow coating on the mine wastes, including jarosite and goethite, is a carrier of the metals. Geochemical and μ-SXRF analyses determined Cu to be the major soil contaminant. μ-SXRF also demonstrated that the heterogeneous nature of the soil chemistry at the micro-meter scale is self-similar to those in the bulk soil samples. Generally metals decreased, with some fluctuations, rapidly downslope through suspension of fines and dissolution in AMD leaving the area of substantial contamination << 0.5 km from the source.

New York↗

Chemical fate and transport of atrazine in soil gravel materials at agrichemical distribution facilities

The gravel commonly used to cover parking lots and roadways at retail agrichemical facilities may contain relatively large concentrations of pesticides that resulted from past management problems. These pesticides may threaten groundwater quality. Previous studies, however, suggested that the pesticides had not moved from the gravel in several sample profiles. Excavations at a closed facility revealed tremendous variability in pesticide distribution within the site. Pesticides were present below the gravel in two profiles, but the mechanism(s) for their movement were not clear. The objectives of this study were to investigate how the physical and chemical properties of the gravel influence the environmental fate of atrazine. All of the gravel samples collected and characterized contained atrazine and sufficient organic C to adsorb significant amounts of atrazine, thus retarding its movement through the gravel. Laboratory column leaching experiments, however, suggested that much of the atrazine should leach from the gravel within a year or two. A field-scale test plot was constructed to study how atrazine moves through the gravel under controlled conditions. Atrazine was “spilled” in the test plot. Atrazine moved from the gravel both vertically and horizontally. It appears that formulated product spilled on gravel will leach. A single discrete spill can give rise to phantom spills whose occurrence and distribution is not related to any specific pesticide-management practice. The apparent lack of atrazine leaching from gravel appeared to be a transient phenomenon and/or the result of sampling limitations in previous studies. The contaminated gravel clearly poses a risk to groundwater quality.

Soil and Sediment Contamination↗

Lead isotopic analyses of selected soil samples from the USEPA Vasquez Blvd.-I-70 study area, Denver, CO

Large amounts of arsenic contamination, in excess of 2000 ppm, have been found in some residential surface soils in northern Denver, Colorado (USEPA, 1999). Associated with the arsenic are elevated levels of metals such as lead, cadmium and mercury. Potential sources of this contamination include waste from smelters in the area and commercial herbicide containing arsenic trioxide and lead arsenate (USEPA, 1999). As a part of the U.S. Environmental Protection Agency’s Vasquez Boulevard-I-70 Project (VBI70 project; USEPA, 1999), lead isotopic analyses of selected soil samples, smelter waste, and a commercial herbicide and a commercial lead arsenate pesticide have been performed in order to constrain the possible sources of elevated lead, and by proxy arsenic, found in these residential soils. The isotopes of lead can be used as a natural tracer in determining sources of contaminants in soils and stream sediments (e.g. Church and others, 1997; Fey and others, 1999; Unruh and others, 2000). The element lead (Pb) consists of four naturally occurring and stable isotopes, 204Pb, 206Pb, 207Pb, and 208Pb. Three of these, 206Pb, 207Pb, and 208Pb are radiogenic decay products of naturally occurring 238U, 235U, and 232Th, respectively. Owing to variations among the U/Pb and Th/Pb elemental abundance ratios among different types of geologic materials, variations in the relative abundances of the Pb isotopes are produced among different materials during geologic time. In order for the Pb isotope method to be useful for determining possible contaminant sources, two important criteria must be met (e.g. Church and others 1997): (1) It must be possible to obtain and measure the Pb isotopic compositions in all potential contaminant sources and in uncontaminated material and (2) the Pb isotopic compositions of the potential contaminant sources must be distinctly different from one another and from uncontaminated background. Variations among the Pb isotopic ratios in selected samples can be correlated with potential sources of Pb with known isotopic compositions in order to determine the relative contribution of Pb from a specific source to the sample. The purpose of this study is to use Pb isotopic data obtained from a selected subset of samples to determine the Pb isotopic signatures of uncontaminated soils as well as those of potential sources of contamination. The data will eventually be used in conjunction with other geochemical data to help determine which source or sources of contamination are most likely responsible for the elevated arsenic levels in the residential soils.

Colorado↗

Characterization of ecological risks at the Milltown Reservoir-Clark Fork River Sediments Superfund Site, Montana

A comprehensive field and laboratory approach to the ecological risk assessment for the Milltown Reservoir-Clark Fork River Sediments Site, a Superfund site in the Rocky Mountains of Montana, has been described in the preceding reports of this series. The risk assessment addresses concerns over the ecological impacts of upstream releases of mining wastes to fisheries of the upper Clark Fork River (CFR) and the benthic and terrestrial habitats further downstream in Milltown Reservoir. The risk characterization component of the process integrated results from a triad of information sources: (a) chemistry studies of environmental media to identify and quantify exposures of terrestrial and aquatic organisms to site-related contaminants; (b) ecological or population studies of terrestrial vegetation, birds, benthic communities, and fish; and (c) in situ and laboratory toxicity studies with terrestrial and aquatic invertebrates and plants, small mammals, amphibians, and fish exposed to contaminated surface water, sediments, wetland soils, and food sources. Trophic transfer studies were performed on waterfowl, mammals, and predatory birds using field measurement data on metals concentrations in environmental media and lower trophic food sources. Studies with sediment exposures were incorporated into the Sediment Quality Triad approach to evaluate risks to benthic ecology. Overall results of the wetland and terrestrial studies suggested that acute adverse biological effects were largely absent from the wetland; however, adverse effects to reproductive, growth, and physiological end points of various terrestrial and aquatic species were related to metals exposures in more highly contaminated depositional areas. Feeding studies with contaminated diet collected from the upper CFR indicated that trout are at high risk from elevated metals concentrations in surface water, sediment, and aquatic invertebrates. Integration of chemical analyses with toxicological and ecological evaluations of metal effects on the wetland and fishery has provided an important foundation for environmental decisions at this site.

Montana↗

Potential soil cleanup objectives for nitrogen-containing fertilizers at agrichemical facilities

Accidental and incidental chemical releases of nitrogen-containing fertilizers occur at retail agrichemical facilities. Because contaminated soil may threaten groundwater quality, the facility may require some type of site remediation. The purpose of this study was to apply the concepts of the Soil Screening Levels of the U.S. Environmental Protection Agency to derive soil cleanup objectives (SCO) that are protective of groundwater quality in Illinois for nitrogen as nitrate and as ammonium. The Soil Screening Levels are based on the solute transport mechanisms of sorption, volatilization, and groundwater dilution, and the contaminant-specific groundwater cleanup objective used to derive the SCO. Because nitrate is relatively unreactive, only groundwater dilution could be taken into account in the derivation of a SCO. Using a default groundwater objective for potable groundwater, an SCO of 38 mg N-NO3/kg was derived. For ammonium, however, the extent of sorption was measured using an uncontaminated, surface-soil sample (0 to 15 cm) of 10 different soil types that occur in Illinois and three gravel-fill samples from three different agrichemical facilities. Using a default groundwater objective, an SCO was derived for each soil type. The median SCO was 989 mg N-NH4/kg. The SCO calculated for each of the 10 soil and 3 fill samples was positively correlated with cation exchange capacity, clay content, and surface area. It was concluded that this approach can be used to derive either default of site-specific SCOs for nitrogen as nitrate and as ammonium for chemical releases. Copyright ?? Taylor & Francis Group, LLC.

Soil and Sediment Contamination↗

Sequestration of hydrophobic organic contaminants by geosorbents

The chemical interactions of hydrophobic organic contaminants (HOCs) with soils and sediments (geosorbents) may result in strong binding and slow subsequent release rates that significantly affect remediation rates and endpoints. The underlying physical and chemical phenomena potentially responsible for this apparent sequestration of HOCs by geosorbents are not well understood. This challenges our concepts for assessing exposure and toxicity and for setting environmental quality criteria. Currently there are no direct observational data revealing the molecular-scale locations in which nonpolar organic compounds accumulate when associated with natural soils or sediments. Hence macroscopic observations are used to make inferences about sorption mechanisms and the chemical factors affecting the sequestration of HOCs by geosorbents. Recent observations suggest that HOC interactions with geosorbents comprise different inorganic and organic surfaces and matrices, and distinctions may be drawn along these lines, particularly with regard to the roles of inorganic micropores, natural sorbent organic matter components, combustion residue particulate carbon, and spilled organic liquids. Certain manipulations of sorbates or sorbent media may help reveal sorption mechanisms, but mixed sorption phenomena complicate the interpretation of macroscopic data regarding diffusion of HOCs into and out of different matrices and the hysteretic sorption and aging effects commonly observed for geosorbents. Analytical characterizations at the microscale, and mechanistic models derived therefrom, are needed to advance scientific knowledge of HOC sequestration, release, and environmental risk.

Environmental Science & Technology↗

Concentrations of polycyclic aromatic hydrocarbons and inorganic constituents in ambient surface soils, Chicago, Illinois: 2001-2002

Samples of ambient surface soils were collected from 56 locations in Chicago, Illinois, using stratified random sampling techniques and analyzed for polycyclic aromatic hydrocarbon (PAH) compounds and inorganic constituents. PAHs appear to be derived primarily from combustion of fossil fuels and may be affected by proximity to industrial operations, but do not appear to be substantially affected by the organic carbon content of the soil, proximity to nonindustrial land uses, or proximity to a roadway. Atmospheric settling of particulate matter appears to be an important mechanism for the placement of PAH compounds into soils. Concentrations of most inorganic constituents are affected primarily by soil-forming processes. Concentrations of lead, arsenic, mercury, calcium, magnesium, phosphorus, copper, molybdenum, zinc, and selenium are elevated in ambient surface soils in Chicago in comparison to the surrounding area, indicating anthropogenic sources for these elements in Chicago soils. Concentrations of calcium and magnesium in Chicago soils appear to reflect the influence of the carbonate bedrock parent material on the chemical composition of the soil, although the effects of concrete and road fill cannot be discounted. Concentrations of inorganic constituents appear to be largely unaffected by the type of nearby land use. Copyright ?? Taylor & Francis Group, LLC.

Soil and Sediment Contamination↗

Arsenic and mercury in the soils of an industrial city in the Donets Basin, Ukraine

Soil and house dust collected in and around Hg mines and a processing facility in Horlivka, a mid-sized city in the Donets Basin of southeastern Ukraine, have elevated As and Hg levels. Surface soils collected at a former Hg-processing facility had up to 1300 mg kg −1 As and 8800 mg kg −1 Hg; 1M HCl extractions showed 74–93% of the total As, and 1–13% of the total Hg to be solubilized, suggesting differential environmental mobility between these elements. In general, lower extractability of As and Hg was seen in soil samples up to 12 km from the Hg-processing facility, and the extractable (1M HCl, synthetic precipitation, deionized water) fractions of As are greater than those for Hg, indicating that Hg is present in a more resistant form than As. The means (standard deviation) of total As and Hg in grab samples collected from playgrounds and public spaces within 12 km of the industrial facility were 64 (±38) mg kg −1 As and 12 (±9.4) mg kg −1 Hg; all concentrations are elevated compared to regional soils. The mean concentrations of As and Hg in dust from homes in Horlivka were 5–15 times higher than dust from homes in a control city. Estimates of possible exposure to As and Hg through inadvertent soil ingestion are provided.

Donets Basin↗

Characterization of the hydrogeologic framework, groundwater-flow system, geochemistry, and aquifer hydraulic properties of the shallow groundwater system in the Wilcox and Lorraine process areas of the Wilcox Oil Company Superfund site near Bristow, Oklahoma, 2022

The Wilcox Oil Company Superfund site (hereinafter referred to as “the site”) was formerly an oil refinery northeast of Bristow in Creek County, Oklahoma. Historical refinery operations contaminated the soil, surface water, streambed sediments, alluvium, and groundwater with refined and stored products at the site. The Wilcox and Lorraine process areas are where the highest concentrations of volatile organic compounds, semivolatile organic compounds, polycyclic aromatic hydrocarbons, and trace elements (including metals) (collectively hereinafter referred to as “contaminants”) were measured in a local shallow perched groundwater system within the alluvium (hereinafter referred to as the “alluvial aquifer”) at the site during previous site assessments. In order to understand the potential migration of contaminants through the soil and groundwater in these areas, the U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, investigated aquifer characteristics of the alluvial aquifer in the Wilcox and Lorraine process areas of the site to (1) document hydraulic conductivity and other aquifer characteristics of the alluvial aquifer that govern contaminant fate and transport, (2) describe the geospatial extent and concentration of the contaminants in the alluvial aquifer in the Wilcox and Lorraine process areas, and (3) describe the geochemical controls pertaining to oxidation and reduction governing the fate and transport and the degradation potential of contaminants in the groundwater. Various data were compiled and collected to evaluate the aquifer characteristics at the site including the hydrogeologic framework, groundwater-flow system, geochemistry, and hydraulic properties of the aquifer. A total of 20 new (2022) groundwater monitoring wells were installed at the site to collect data used to supplement groundwater-level altitude and groundwater-quality data collected from older, existing groundwater monitoring wells and piezometers. Data compiled and collected for the study were used to evaluate the characteristics of the alluvial aquifer at the site. These aquifer characteristics are defined by the hydrogeologic framework, groundwater-flow system, geochemistry, and hydraulic properties of the aquifer.

Oklahoma↗

Modeling aeolian transport in response to succession, disturbance and future climate: Dynamic long-term risk assessment for contaminant redistribution

Aeolian sediment transport is a fundamental process redistributing sediment, nutrients, and contaminants in dryland ecosystems. Over time frames of centuries or longer, horizontal sediment fluxes and associated rates of contaminant transport are likely to be influenced by succession, disturbances, and changes in climate, yet models of horizontal sediment transport that account for these fundamental factors are lacking, precluding in large part accurate assessment of human health risks associated with persistent soil-bound contaminants. We present a simple model based on empirical measurements of horizontal sediment transport (predominantly saltation) to predict potential contaminant transport rates for recently disturbed sites such as a landfill cover. Omnidirectional transport is estimated within vegetation that changes using a simple Markov model that simulates successional trajectory and considers three types of short-term disturbances (surface fire, crown fire, and drought-induced plant mortality) under current and projected climates. The model results highlight that movement of contaminated soil is sensitive to vegetation dynamics and increases substantially (e.g., > fivefold) when disturbance and/or future climate are considered. The time-dependent responses in horizontal sediment fluxes and associated contaminant fluxes were sensitive to variability in the timing of disturbance, with longer intervals between disturbance allowing woody plants to become dominant and crown fire and drought abruptly reducing woody plant cover. Our results, which have direct implications for contaminant transport and landfill management in the specific context of our assessment, also have general relevance because they highlight the need to more fully account for vegetation dynamics, disturbance, and changing climate in aeolian process studies.

Aeolian Research↗

Mercury in waters, soils, and sediments of the New Jersey Coastal Plain: A comparison of regional distribution and mobility with the mercury contamination at the William J. Hughes Technical Center, Atlantic County, New Jersey

Mercury in soils, surface water, and groundwater at the William J. Hughes Technical Center , Atlantic County, New Jersey, has been found at levels that exceed established background concentrations in Coastal Plain waters, and, in some cases, New Jersey State standards for mercury in various media. As of 2012, it is not known whether this mercury is part of regional mercury contamination or whether it is related to former military activities. Regionally, groundwater supplying about 700 domestic wells in the New Jersey Coastal Plain is contaminated with mercury that appears to be derived from anthropogenic inputs, such as agricultural pesticide use and atmospheric deposition. High levels of mercury occasionally are found in Coastal Plain soils, but disturbance during residential development on former agricultural land is thought to have mobilized any mercury applied during farming, a hypothesis borne out by experiments leaching mercury from soils. In the unsewered residential areas with mercury-contaminated groundwater, septic-system effluent is believed to create reducing conditions in which mercury sorbed to subsoils is mobilized to groundwater. In comparing the levels of mercury found in soils, sediments, streamwater, and groundwater at the William J. Hughes Technical Center site with those found regionally, mercury concentrations in groundwater in the region are, in some cases, substantially higher than those found in groundwater at the William J. Hughes Technical Center site. Nevertheless, concentrations of mercury in streamwater at the site are, in some instances, higher than most found regionally. The mercury contents in soils and sediment at the William J. Hughes Technical Center site are substantially higher than those found to date (2012) in the region, indicating that a source other than regional sources may be present at the site.

New Jersey↗

Mobilization and attenuation of metals downstream from a base-metal mining site in the Matra Mountains, northeastern Hungary

Regional geochemical baseline values have been established for Hungary by the use of low-density stream-sediment surveys of flood-plain deposits of large drainage basins and of the fine fraction of stream sediments. The baseline values and anomaly thresholds thus produced helped to evaluate the importance of high toxic element concentrations found in soils in a valley downstream of a polymetallic vein-type base-metal mine. Erosion of the mine dumps and flotation dump, losses of metals during filtering, storage and transportation, human neglects, and operational breakdowns, have all contributed to the contamination of a small catchment basin in a procession of releases of solid waste. The sulfide-rich waste material weathers to a yellow color; this layer of 'yellow sand' blankets a narrow strip of the floodplain of Toka Creek in the valley near the town of Gyongyosoroszi. Contamination was spread out in the valley by floods. Metals present in the yellow sand include Pb, As, Cd, Cu, Zn, and Sb. Exposure of the local population to these metals may occur through inhalation of airborne particulates or by ingestion of these metals that are taken up by crops grown in the valley. To evaluate the areal extent and depth of the contamination, active stream sediment, flood-plain deposits, lake or reservoir sediments, soils, and surface water were sampled along the erosion pathways downstream of the mine and dumps. The flood-plain profile was sampled in detail to see the vertical distribution of elements and to relate the metal concentrations to the sedimentation and contamination histories of the flood plain. Downward migration of mobile Zn and Cd from the contaminated upper layers under supergene conditions is observed, while vertical migration of Pb, As, Hg and Sb appears to be insignificant. Soil profiles of 137Cs which originated from above-ground atomic bomb tests and the Chernobyl accident, provide good evidence that the upper 30-40 cm of the flood-plain sections, which includes the yellow sand contamination, were deposited in the last 30-40 years.The regional geochemical baseline values are established for Hungary using low-density stream-sediment surveys of flood-plain deposits of large drainage basins and of the fine fraction of stream sediments. The baseline values and anomaly thresholds allowed the evaluation of the importance of high toxic element concentrations in soils in a valley, downstream of a polymetallic vein-type base-metal mine. The metals present in the yellow sand include Pb, As, Cd, Cu, Zn and Sb. To evaluate the areal extent and depth of the contamination, active stream sediment, flood-plain deposits, lake or reservoir sediments, the soils and surface water were sampled along the erosion pathways downstream of the mine and dumps.

Journal of Geochemical Exploration↗

Coeur d'Alene Lake, Idaho: Insights gained From limnological studies of 1991-92 and 2004-06

More than 100 years of mining and processing of metal-rich ores in northern Idaho’s Coeur d’Alene River basin have resulted in widespread metal contamination of the basin’s soil, sediment, water, and biota, including Coeur d’Alene Lake. Previous studies reported that about 85 percent of the bottom of Coeur d’Alene Lake is substantially enriched in antimony, arsenic, cadmium, copper, lead, mercury, silver, and zinc. Nutrients in the lake also are a major concern because they can change the lake’s trophic status—or level of biological productivity—which could result in secondary releases of metals from contaminated lakebed sediments. This report presents insights into the limnological functioning of Coeur d’Alene Lake based on information gathered during two large-scale limnological studies conducted during calendar years 1991–92 and water years 2004–06. Both limnological studies reported that longitudinal gradients exist from north to south for decreasing water column transparency, loss of dissolved oxygen, and increasing total phosphorus concentrations. Gradients also exist for total lead, total zinc, and hypolimnetic dissolved oxygen concentrations, ranging from high concentrations in the central part of the lake to lower concentrations at the northern and southern ends of the lake. In the southern end of the lake, seasonal anoxia serves as a mechanism to release dissolved constituents such as phosphorus, nitrogen, iron, and manganese from lakebed sediments and from detrital material within the water column. Nonparametric statistical hypothesis tests at a significance level of α=0.05 were used to compare analyte concentrations among stations, between lake zones, and between study periods. The highest dissolved oxygen concentrations were measured in winter in association with minimum water temperatures, and the lowest concentrations were measured in the Coeur d’Alene Lake hypolimnion during late summer or autumn as prolonged thermal stratification restricted mixing of the oxygenated upper water column and the hypolimnion, where oxygen was consumed. Large differences in median concentrations of dissolved inorganic nitrogen were measured between the euphotic zone and hypolimnion in the deep areas of the lake. These differences in nitrogen concentrations were attributable to several limnological processes, including seasonal inflow plume routing, isolation from wind-driven circulation and associated hypolimnetic enrichment, phytoplanktonic assimilation during summer months, and benthic flux. Increased chlorophyll- a and total phosphorus concentrations were measured throughout the lake in the 2004–06 study compared with results from the 1991–92 study. No significant change in hypolimnetic dissolved inorganic nitrogen concentration throughout the lake was noted even though total nitrogen loads into the lake decreased between study periods. Total zinc and total lead decreased throughout the lake from the 1991-92 study to the 2004-06 study except in the southern part of the lake, where concentrations were typically low. Median detected nitrogen-to-phosphorus ratios decreased from the 1991–92 study to the 2004–06 study. Whereas the lake was clearly phosphorus-limited in 1991–92, in 2004–06 the lake may have been much closer to the boundary value of 7.2 that separates nitrogen from phosphorus limitation. However, due to changes in analytical reporting limits in the period between the two studies, the data are insufficiently certain to draw reliable conclusions with regard to limiting nutrients. For both studies, the trophic state of the lake was classified as oligotrophic (less productive) or mesotrophic (moderately productive), depending on the constituent used for classification. Internal circulation from wind-generated waves and changes in the lake’s thermocline are important processes for distribution of water-quality constituents throughout Coeur d’Alene Lake. Surficial distribution of trace metals throughout most of the lake, including bays, is relatively uniform. Even south of the Coeur d’Alene River mouth, lakebed sediments are contaminated with trace metals. Inflow plume routing of the two primary inflow sources, the Coeur d’Alene and St. Joe Rivers, also significantly affects the fate and transport of contaminants. Most riverine inflows appear to move through the lake as overflow during summer, interflow during spring and autumn, and underflow during winter. Benthic flux is another key transport process for contaminants in Coeur d’Alene Lake. The results of in situ benthic flux chamber experiments indicated movement of dissolved metals, nutrients, and dissolved organic carbon out of the lakebed sediments. However, the lake is an overall sink for these constituents when they are associated with particulate material.

Idaho↗

Hydrogeologic framework, hydrology, and refined conceptual model of groundwater flow for Coastal Plain aquifers at the Standard Chlorine of Delaware, Inc. Superfund Site, New Castle County, Delaware, 2005-12

From 1966 to 2002, activities at the Standard Chlorine of Delaware chemical facility in New Castle County, Delaware resulted in the contamination of groundwater, soils, and wetland sediment. In 2005, the U.S. Geological Survey (USGS), in partnership with the U.S. Environmental Protection Agency, Region 3, and the Delaware Department of Natural Resources and Environmental Control began a multi-year investigation of the hydrogeologic framework and hydrology of the confined aquifer system. The goals of the ongoing study at the site (the Potomac Aquifer Study) are to determine the hydraulic connection between the Columbia and Potomac aquifers, determine the direction of groundwater flow in the Potomac aquifer, and identify factors affecting the fate of contaminated groundwater. This report describes progress made towards these goals based on available data collected through September 2012. The regional hydrogeologic framework indicates that the site is underlain by Coastal Plain sediments of the Columbia, Merchantville, and Potomac Formations. Two primary aquifers underlying the site, the Columbia and the upper Potomac, are separated by the Merchantville Formation confining unit. Local groundwater flow in the surficial (Columbia) aquifer is controlled by topography and generally flows northward and discharges to nearby surface water. Regional flow within the Potomac aquifer is towards the southeast, and is strongly influenced by major water withdrawals locally. Previous investigations at the site indicated that contaminants, primarily benzene and chlorinated benzene compounds, were present in the Columbia aquifer in most locations; however, there were only limited detections in the upper Potomac aquifer as of 2004. From 2005 through 2012, the USGS designed a monitoring network, assisted with exploratory drilling, collected data at monitoring wells, conducted geophysical surveys, evaluated water-level responses in wells during pumping of a production well, and evaluated major aquifer withdrawals. Data collected through these efforts were used to refine the local conceptual flow system. The refined conceptual flow system for the site includes: (a) identification of gaps in confining units in the study area, (b) identification and correlation of multiple water-bearing sand intervals within the upper Potomac Formation, (c) connections between groundwater and surface water, (d) connections between shallow and deeper groundwater, (e) new water-level (or potentiometric surface) maps and inferred flow directions, and (f) identification of major local pumping well influences. The implications of the revised conceptual flow system on the occurrence and movement of site contaminants are that the resulting detection of contaminants in the upper Potomac aquifer at specific well locations can be attributed primarily to either advective lateral transport, direct vertical contaminant transport, or a combination of vertical and lateral movement resulting from changes in water withdrawal rates over time.

Delaware↗

Antimony in mine wastes: Geochemistry, mineralogy, microbiology

Antimony (Sb) is a valuable mined commodity, used mostly in fire retardants, and considered a critical element. It is also a potential environment hazard classed as a carcinogen. Antimony is concentrated in tailings and waste rock from Sb mines as well as other locations, such as precious metal deposits, where Sb is present in the ore but not recovered. This review covers the aqueous geochemistry, isotope chemistry, mineralogy, and microbiology of Sb in the context of mine waste. The primary minerals stibnite and sulfosalts may release Sb in surface and groundwaters and result in contamination of soils, plants, and river sediments. In some cases, Sb mobility is limited by its adsorption and incorporation into Fe (oxyhydr)oxides. At higher Sb concentrations, precipitation of Sb secondary hosts such as tripuhyite (FeSbO 4 , relatively insoluble) and brandholzite (Mg[Sb(OH) 6 ] 2 · 6H 2 O, highly soluble) influence Sb concentrations in water associated with mine waste. Although Sb is nonessential to organisms, microorganisms are involved in oxidation, reduction, and methylation processes that can drive biogeochemical transformations. Limited toxicological information about Sb makes it challenging to establish regulations or guidelines limiting the concentration of Sb. Antimony is frequently associated with arsenic in mine waste, and remediation design is often based on the assumption that both metalloids behave in a similar way. However, new research suggests that in some environments, this is not the case, and Sb should be considered based on its unique biogeochemical behavior.

Economic Geology↗

Depth-dependent soil mixing persists across climate zones

Soil mixing over long (>10 2 y) timescales enhances nutrient fluxes that support soil ecology, contributes to dispersion of sediment and contaminated material, and modulates fluxes of carbon through Earth’s largest terrestrial carbon reservoir. Despite its foundational importance, we lack robust understanding of the rates and patterns of soil mixing, largely due to a lack of long-timescale data. Here we demonstrate that luminescence, a light-sensitive property of minerals used for geologic dating, can be used as a long-timescale sediment tracer in soils to reveal the structure of soil mixing. We develop a probabilistic model of transport and mixing of tracer particles and associated luminescence in soils and compare with a global compilation of luminescence versus depth in various locations. The model–data comparison reveals that soil mixing rate varies over the soil depth, with this depth dependency persisting across climate and ecological zones. The depth dependency is consistent with a model in which mixing intensity decreases linearly or exponentially with depth, although our data do not resolve between these cases. Our findings support the long-suspected idea that depth-dependent mixing is a spatially and temporally persistent feature of soils. Evidence for a climate control on the patterns and intensities of soil mixing with depth remains elusive and requires the further study of soil mixing processes.

PNAS↗

Geohydrology and water quality of the Durham Center Area, Durham, Connecticut

Contaminated ground water is widespread and persistent beneath the Durham Center area in the town of Durham, Conn. Most of the contaminants are organic halides, usually trichloroethene, 1,1,1-trichloroethane, and tetrachloroethene. Less extensive chemical contamination of surface water, soil, and glacial sediments also has been detected. Two manufacturing companies, located at the northern and southern ends of this largely residential area, are believed to be the principal sources of the organic compounds detected in ground water. The contamination of water in the bedrock, the primary source of drinking water throughout the area, is the major environmental concern. Maximum concentrations of trichloroethene in three bed- rock wells range from 4,500 to about 5,500 mg/L (micrograms per liter). Concentrations of trichloroethene greater than 5 mg/L, the maximum contaminant level established for drinking water by the U.S Environmental Protection Agency, have regularly been detected in water samples from many other bedrock wells for at least 9 years. The geohydrology of the area is highly complex. Compact lodgment till that is up to 30 feet thick and probably fractured, overlies the bedrock. The bedrock is lithologically heterogeneous, and con- sists mostly of red fluvial sandstone, siltstone, and conglomerate; it is locally interbedded with black lacustrine shales and gray sandstones. Lithology and stratigraphy interpreted from borehole-geophysical logs at Durham Center are consistent with the Portland Formation subfacies described in earlier geologic studies. Beds strike nearly north-south and dip gently eastward. At least one high-angle normal fault transects the bedrock; it strikes northeast and dips northwest. Acoustic televiewer logs, measurements at out-crops, and azimuthal, square-array, resistivity data indicate a dominance of northeast-striking fractures that dip steeply northwest and southeast. Less prevalent strike directions are north to east-north-east. The till and sedimentary bedrock are dual-porosity, dual-permeability media. The hydraulic conductivity of the bulk mass of till is believed to be on the order of tenths of a foot per day to about 2.5 feet per day, with a total porosity of about 25 percent and an estimated average fracture porosity of less than 1 percent. The reported transmissivities of the bedrock range from less than 1 to about 17,000 feet squared per day and storativity is generally about 10-4, but the accuracy of these values is uncertain. The intergranular porosity of the sandstone units is estimated to average 5 percent, and estimates of fracture porosity from square-array, resistivity soundings at two sites were 1.1 and 2.7 percent. The bedrock has characteristics of both a single aquifer and a multi-unit, artesian or leaky aquifer system. A local ground-water-flow system that includes the upper part of the bedrock is unconfined. A large- scale flow system in deeper parts of the bedrock has transported organic compounds across topographic drainage divides. Borehole-geophysical logs and head measurements indicate that the natural ground- water-flow system in the bedrock has been altered by drilled wells that connect fractures and by with- drawals from wells. A conceptual model of the movement and fate of organic contaminants suggests that (1) nonaqueous phase organic halides are retained near their source; (2) flow is primarily through fractures in the till and through fractures and bedding-plane openings in the sedimentary rocks; (3) retardation of contaminants occurs primarily by diffusion from fractures into the aquifer matrix; and (4) transport directions of dissolved organic halides are controlled by a combination of natural hydraulic gradients, hydraulic gradients produced by the cyclical pumping of wells, and by the strike directions of bedrock faults, fractures, and bedding planes.

Connecticut↗

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↗