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Potentially bioavailable natural organic carbon and hydrolyzable amino acids in aquifer sediments

This study evaluated the relationship between concentrations of operationally defined potentially bioavailable organic -carbon (PBOC) and hydrolyzable amino acids (HAAs) in sediments collected from a diverse range of chloroethene--contaminated sites. Concentrations of PBOC and HAA were measured using aquifer sediment samples collected at six selected study sites. Average concentrations of total HAA and PBOC ranged from 1.96 ± 1.53 to 20.1 ± 25.6 mg/kg and 4.72 ± 0.72 to 443 ± 65.4 mg/kg, respectively. Results demonstrated a statistically significant positive relationship between concentrations of PBOC and total HAA present in the aquifer sediment (p < 0.05). Higher levels of HAA were consistently observed at sites with greater levels of PBOC and first-order decay rates. Because amino acids are known to be readily biodegradable carbon compounds, this relationship suggests that the sequential chemical extraction procedure used to measure PBOC is a useful indicator of bioavailable carbon in aquifer sediments. This, in turn, is consistent with the interpretation that PBOC measurements can be used for estimating the amount of natural organic carbon available for driving the reductive dechlorination of chloroethenes in groundwater systems.

Ground Water Monitoring and Remediation

Evaluation of landslide monitoring in the Polish Carpathians

In response to the June 15, 2010 request from the Polish Geological Institute (PGI) to the U.S. Geological Survey (USGS) for assistance and advice regarding real-time landslide monitoring, landslide specialists from the USGS Landslide Hazard Program visited PGI headquarters and field sites in September 2010. During our visit we became familiar with characteristics of landslides in the Polish Carpathians, reviewed PGI monitoring techniques, and assessed needs for monitoring at recently activated landslides. Visits to several landslides that are monitored by PGI (the Just, Hańczowa, Szymbark, Siercza and Łasńica landslides) revealed that current data collection (monthly GPS and inclinometer surveys, hourly piezometers readings) is generally sufficient for collecting basic information about landslide displacement, depth, and groundwater conditions. Large landslides are typically hydrologically complex, and we would expect such complexity in Carpathian landslides, given the alternating shale and sandstone stratigraphy and complex geologic structures of the flysch bedrock. Consequently groundwater observations could be improved by installing several piezometers that sample the basal shear zone of each landslide being monitored by PGI. These could be supplemented by additional piezometers at shallower depths to help clarify general flow directions and hydraulic gradients. Remedial works at Hańczowa make the landslide unsuitable for monitoring as part of an early warning network. Monitoring there should focus on continued performance of the remedial works. Our suggestions for new monitoring at recently activated landslides are summarized in table 1. Displacement monitoring using extensometers and (or) GPS is a high priority at Kłodne, Łaśnica, Łazki, and Siedloki. Geomorphologic mapping of active surface features (scarps, cracks, shear zones, folds, and thrusts) in sufficient detail to reveal the kinematics of each landslide would greatly help in planning subsurface exploration and monitoring. Mapping should take advantage of existing and future airborne lidar data sets of specific areas, where available. Borehole inclinometers and piezometers would complete the basic monitoring package for these landslides. The landslide at Kłodne may be well suited for more detailed monitoring for landslide process research, although research opportunities exist at the other landslides as well. The landslide near Siedloki may be a good candidate for terrestrial laser scanning (TLS). Tandem streamflow gages upstream and downstream from the Siedloki landslide, or laser distance meters to monitor advancement of the toe, may be needed to provide warning of stream blockage of Potok Milowski. A real-time warning system specifically for the Łazki landslide might be considered due to potential concerns about catastrophic movement into Międzybrodzie Reservoir. Challenges associated with the establishment of a complete real-time monitoring and early warning system are far greater than just the technical and logistical aspects of installing remote monitoring systems at a large number of landslides. Long-term maintenance of a landslide monitoring network will involve considerable effort and expense as sensors break-down from exposure to weather, landslide movement, and harsh underground environmental conditions. Once PGI&rsquo;s planned pilot network of 10-20 monitored landslides is operating, a period of observation and analysis will be needed to establish appropriate alert levels and criteria for issuing alerts and warnings. Simultaneously, discussions with authorities will be needed to develop action plans for responding to landslide notifications and (or) warnings. Public resistance to landslide warnings and mandated evacuations may be high given the low historical incidence of fatalities and injuries resulting from Carpathian landslides and the small potential for warnings to reduce landslide damage to homes and land. Careful weighing of purpose, advantages, and costs of a large-scale monitoring and early warning program is needed early in the planning process and should be revisited regularly throughout pilot and final implementation. In this report, we present a generic plan for monitoring of a hypothetical Carpathian landslide that illustrates how our suggestions for each of the specific landslides could be implemented. The plan includes basic pore pressure, displacement, and weather monitoring, along with supplemental monitoring for special conditions at specific landslides. Table 2 summarizes the overall approach and basic equipment and software requirements.

Open-File Report

Biodegradation of chloroethene compounds in groundwater at Operable Unit 1, Naval Undersea Warfare Center, Division Keyport, Washington, 1999-2010

The U.S. Geological Survey evaluated the biodegradation of chloroethene compounds in groundwater beneath the former landfill at Operable Unit 1 (OU 1) of the U.S. Naval Undersea Warfare Center (NUWC), Division Keyport. The predominant contaminants in groundwater are the chloroethene compounds trichloroethene, cis -1,2-dichloroethene, and vinyl chloride. The remedy selected for groundwater contamination at OU 1 includes phytoremediation and natural attenuation. In 1999, the U.S. Navy planted two hybrid poplar plantations, referred to as the northern and southern plantations, over the most contaminated parts of the landfill. The U.S. Navy monitors tree health, groundwater levels, and contaminant concentrations to assess the effectiveness of phytoremediation. The U.S. Geological Survey began a cooperative effort with the U.S. Navy in 1995 to monitor the effectiveness of natural attenuation processes for removing and controlling the migration of chloroethenes and chloroethanes. Field and laboratory studies from 1996 through 2000 demonstrated that biodegradation of chloroethenes and chloroethanes in shallow groundwater at OU 1 was substantial. The U.S. Geological Survey monitored geochemical and contaminant concentrations in groundwater annually from 2001 through 2010. This report presents groundwater geochemical and contaminant data collected by the U.S. Geological Survey during June 2010 and evaluates evidence for continued biodegradation of chloroethenes in groundwater. Geochemical and contaminant concentration data through 2010 indicate that biodegradation of chloroethenes in groundwater continued beneath the landfill at OU 1. Contaminant concentrations in groundwater decreased beneath most of the 9-acre landfill between 1999 and 2010. The evidence indicating that biodegradation was a primary cause for the decreased concentrations included decreasing ratios of more highly chlorinated compounds to less chlorinated compounds over time, and widespread detections of non-chlorinated biodegradation end-products ethane and ethene. No widespread changes in groundwater reduction-oxidation (redox) conditions were observed that could result in either more or less efficient biodegradation. Even with continued biodegradation, dissolved-phase contaminant concentrations in the tens of milligrams per liter have persisted beneath part of the 0.7-acre southern plantation. The magnitude and persistence of those concentrations indicate that non-aqueous phase liquid chloroethenes likely are present beneath the southern plantation and are not substantially affected by biodegradation. During 2010, chloroethenes continued to be measured in shallow groundwater samples from the southern part of the adjacent marsh, although at the lowest concentrations ever measured. Flux calculations based on 2010 data indicate that 95 percent of dissolved-phase chloroethenes in the upper aquifer beneath the southern landfill were degraded before discharging to surface water. Overall, biodegradation of chloroethenes in groundwater throughout OU 1 continued through 2010, and it prevented most of the mass of dissolved-phase chloroethenes in the upper aquifer beneath the landfill from discharging to surface water.

Washington

Sewers as a source and sink of chlorinated-solvent groundwater contamination, Marine Corps Recruit Depot, Parris Island, South Carolina

Groundwater contamination by tetrachloroethene and its dechlorination products is present in two partially intermingled plumes in the surficial aquifer near a former dry‐cleaning facility at Site 45, Marine Corps Recruit Depot, Parris Island, South Carolina. The northern plume originates from the vicinity of former above‐ground storage tanks. Free‐phase tetrachloroethene from activities in this area entered the groundwater. The southern plume originates at a nearby, new dry‐cleaning facility, but probably was the result of contamination released to the aquifer from a leaking sanitary sewer line from the former dry‐cleaning facility. Discharge of dissolved groundwater contamination is primarily to leaking storm sewers below the water table. The strong influence of sanitary sewers on source distribution and of storm sewers on plume orientation and discharge at this site indicates that groundwater‐contamination investigators should consider the potential influence of sewer systems at their sites.

South Carolina

Distributional patterns of arsenic concentrations in contaminant plumes offer clues to the source of arsenic in groundwater at landfills

The distributional pattern of dissolved arsenic concentrations from landfill plumes can provide clues to the source of arsenic contamination. Under simple idealized conditions, arsenic concentrations along flow paths in aquifers proximal to a landfill will decrease under anthropogenic sources but potentially increase under in situ sources. This paper presents several conceptual distributional patterns of arsenic in groundwater based on the arsenic source under idealized conditions. An example of advanced subsurface mapping of dissolved arsenic with geophysical surveys, chemical monitoring, and redox fingerprinting is presented for a landfill site in New Hampshire with a complex flow pattern. Tools to assist in the mapping of arsenic in groundwater ultimately provide information on the source of contamination. Once an understanding of the arsenic contamination is achieved, appropriate remedial strategies can then be formulated.

Remediation Journal

Analyses of regulatory water-quality data

Between 1952 and 1964, hexavalent chromium, Cr(VI), was released into groundwater from the Pacific Gas and Electric Company (PG&E) Hinkley compressor station in the Mojave Desert 80 miles northeast of Los Angeles, California. The Pacific Gas and Electric Company has monitored groundwater near Hinkley, California, for Cr(VI) and other constituents since the late 1980s. By June 2017, more than 20,000 samples had been collected and analyzed for Cr(VI) for regulatory purposes. Most Cr(VI) samples were analyzed using the U.S. Environmental Protection Agency (EPA) Method 218.6 with a laboratory reporting level (LRL) of 0.2 micrograms per liter (μg/L). Between July 2012 and June 2017, selected samples were analyzed for low-level Cr(VI) concentrations using a modified version of EPA Method 218.6 with an LRL of 0.06 μg/L. Field-blank data and duplicate samples collected during this period indicate a study reporting level (SRL) of 0.2 μg/L for most analyses and a SRL of 0.12 μg/L for low-level Cr(VI) analyses. The overall precision for Cr(VI) data analyzed by both methods at the interim regulatory Cr(VI) background concentration of 3.1 μg/L was 0.09 μg/L, or about 3 percent. Hexavalent chromium concentration trends were calculated for 564 monitoring wells for the period from July 2012 through June 2017. Upward Cr(VI) concentration trends were present in water from 102 monitoring wells throughout Hinkley and Water Valleys. Upward Cr(VI) concentration trends in water from wells near the margins of the October–December 2015 (Q4 2015) regulatory Cr(VI) plume (1) within strands of the Lockhart fault east and southeast of the Hinkley compressor station and (2) in water from shallow wells within the northern subarea were consistent with expansion of the Cr(VI) plume in these areas between 2012 and 2017. Upward Cr(VI) concentration trends were widely distributed elsewhere in Hinkley and Water Valleys outside the Q4 2015 regulatory Cr(VI) plume and were commonly associated with declining water levels. These upward trends may result from natural Cr(VI) sources, including movement of Cr(VI) containing groundwater from (1) weathered bedrock, (2) fine-textured deposits, or (3) secondarily oxidized material distributed throughout aquifer deposits. Downward Cr(VI) concentration trends were observed in 146 monitoring wells. Downward trends were largely within the Q4 2015 regulatory Cr(VI) plume and can be attributed to remediation activities downgradient from the Hinkley compressor station. Hexavalent chromium concentration trends also were calculated for 219 domestic wells from July 2012 through June 2017. Upward Cr(VI) concentration trends in 8 domestic wells and downward trends in 23 domestic wells were clustered largely within former residential areas west of the Q4 2015 regulatory Cr(VI) plume. Results of Cr(VI) trend analyses (including upward, downward, and no trend) were used with other data as part of a summative-scale analysis (chapter G) to define the extent of anthropogenic Cr(VI) and natural Cr(VI) within Hinkley and Water Valleys.

California

Monitoring the effect of poplar trees on petroleum-hydrocarbon and chlorinated-solvent contaminated ground water

At contaminated groundwater sites, poplar trees can be used to affect ground-water levels, flow directions, and ultimately total groundwater and contaminant flux to areas downgradient of the trees. The magnitude of the hydrologic changes can be monitored using fundamental concepts of groundwater hydrology, in addition to plant physiology-based approaches, and can be viewed as being almost independent of the contaminant released. The affect of poplar trees on the fate of groundwater contaminants, however, is contaminant dependent. Some petroleum hydrocarbons or chlorinated solvents may be mineralized or transformed to innocuous compounds by rhizospheric bacteria associated with the tree roots, mineralized or transformed by plant tissues in the transpiration stream or leaves after uptake, or passively volatilized and rapidly dispersed or oxidized in the atmosphere. These processes also can be monitored using a combination of physiological- or geochemical-based field or laboratory approaches. When combined, such hydrologic and contaminant monitoring approaches can result in a more accurate assessment of the use of poplar trees to meet regulatory goals at contaminated groundwater sites, verify that these goals continue to be met in the future, and ultimately lead to a consensus on how the performance of plant-based remedial strategies (phytoremediation) is to be assessed.

International Journal of Phytoremediation

Streamflow Gain and Loss, Hydrograph Separation, and Water Quality of Abandoned Mine Lands in the Daniel Boone National Forest, Eastern Kentucky, 2015–17

During 2015–17, the U.S. Geological Survey, in cooperation with the U.S. Department of Agriculture Forest Service (Forest Service), carried out a study to characterize the hydrology and water chemistry in two study areas within the Daniel Boone National Forest. One study area was within the Rock Creek drainage and the other study area included the Wildcat and Addison Branch drainages. Both study areas historically were mined for coal prior to the Surface Mining Control and Reclamation Act of 1977 and contain abandoned coal mine sites that have since been the focus of remediation efforts. Synoptic surveys of streamflow and water-quality properties (water temperature, pH, specific conductance, and dissolved oxygen) of Rock Creek were done during November 2015 and May 2016, and surveys of Wildcat and Addison Branches were done during June 2016 and May 2017. Streamflow measurements were used to quantify contributions from tributaries and to compute streamflow gain and loss in designated reaches. Discrete measurements of water temperature, pH, specific conductance, and dissolved oxygen were used to evaluate conditions during a short timeframe and for comparison between study areas. Study designs for the two study areas differed because there was an operating streamgage on Rock Creek near Yamacraw, Kentucky (station number 03410590) where streamflow and water-quality properties (water temperature, specific conductance, pH, dissolved oxygen, and turbidity) were monitored continuously, while Addison and Wildcat Branches were ungaged. Several hydrograph separation methods were used to estimate base flow and runoff at the Rock Creek gage. These data will be used by the Forest Service to evaluate the current (2018) conditions and plan remediation efforts. The water quality at Rock Creek was less affected by acid mine drainage (AMD) than the Wildcat or Addison Branches. Appreciable losing reaches, where water flowed underground, were identified in both study areas. All losing reaches coincided with karst topography. Streamflow increased in areas with openings to underground mine tunnels, known as portals. Six hydrograph separation methods (Base-flow index [BFI; standard and modified], HYSEP [fixed interval, sliding interval, and local minimum], and PART) were applied to daily mean streamflow collected from August 2015 to August 2017 at station number 03410590. The hydrograph separation methods partition total streamflow into base flow and streamflow that originated from surface runoff. Base flow typically reacts slowly to precipitation infiltration and is largely sustained by groundwater discharge. The estimated daily base flow and runoff made with the different separation methods are not highly different. On average, base flow accounted for more total streamflow than surface runoff during the study period, irrespective of method. Water temperature, pH, dissolved oxygen, specific conductance, and turbidity values were measured from July 2016 through July 2017 with a continuous monitor installed at station number 03410590. Nearly neutral pH values that ranged from 6.8 to 7.9 standard units likely limited metal solubility in the surface water. The continuous specific conductance values ranged between 30 and 259 microsiemens per centimeter at 25 degrees Celsius. The previous remediation efforts are likely continuing to improve the effect of AMD in the study area.

Kentucky

Hydrogeologic framework of fractured sedimentary rock, Newark Basin, New Jersey

The hydrogeologic framework of fractured sedimentary bedrock at the former Naval Air Warfare Center (NAWC), Trenton, New Jersey, a trichloroethylene (TCE)-contaminated site in the Newark Basin, is developed using an understanding of the geologic history of the strata, gamma-ray logs, and rock cores. NAWC is the newest field research site established as part of the U.S. Geological Survey Toxic Substances Hydrology Program, Department of Defense (DoD) Strategic Environmental Research and Development Program, and DoD Environmental Security Technology Certification Program to investigate contaminant remediation in fractured rock. Sedimentary bedrock at the NAWC research site comprises the Skunk Hollow, Byram, and Ewing Creek Members of the Lockatong Formation and Raven Rock Member of the Stockton Formation. Muds of the Lockatong Formation that were deposited in Van Houten cycles during the Triassic have lithified to form the bedrock that is typical of much of the Newark Basin. Four lithotypes formed from the sediments include black, carbon-rich laminated mudstone, dark-gray laminated mudstone, light-gray massive mudstone, and red massive mudstone. Diagenesis, tectonic compression, off-loading, and weathering have altered the rocks to give some strata greater hydraulic conductivity than other strata. Each stratum in the Lockatong Formation is 0.3 to 8 m thick, strikes N65 degrees E, and dips 25 degrees to 70 degrees NW. The black, carbon-rich laminated mudstone tends to fracture easily, has a relatively high hydraulic conductivity and is associated with high natural gamma-ray count rates. The dark-gray laminated mudstone is less fractured and has a lower hydraulic conductivity than the black carbon-rich laminated mudstone. The light-gray and the red massive mudstones are highly indurated and tend to have the least fractures and a low hydraulic conductivity. The differences in gamma-ray count rates for different mudstones allow gamma-ray logs to be used to correlate and delineate the lithostratigraphy from multiple wells. Gamma-ray logs and rock cores were correlated to develop a 13-layer gamma-ray stratigraphy and 41-layer lithostratigraphy throughout the fractured sedimentary rock research site. Detailed hydrogeologic framework shows that black carbon-rich laminated mudstones are the most hydraulically conductive. Water-quality and aquifer-test data indicate that groundwater flow is greatest and TCE contamination is highest in the black, carbon- and clay-rich laminated mudstones. Large-scale groundwater flow at the NAWC research site can be modeled as highly anisotropic with the highest component of permeability occurring along bedding planes.

New Jersey

Application of a new vertical profiling tool (ESASS) for sampling groundwater quality during hollow-stem auger drilling

A new tool called ESASS (Enhanced Screen Auger Sampling System) was developed by the U.S. Geological Survey. The use of ESASS, because of its unique U.S. patent design (U.S. patent no. 7,631,705 B1), allows for the collection of representative, depth-specific groundwater samples (vertical profiling) in a quick and efficient manner using a 0.305-m long screen auger during hollow-stem auger drilling. With ESASS, the water column in the flights above the screen auger is separated from the water in the screen auger by a specially designed removable plug and collar. The tool fits inside an auger of standard inner diameter (82.55 mm). The novel design of the system constituted by the plug, collar, and A-rod allows the plug to be retrieved using conventional drilling A-rods. After retrieval, standard-diameter (50.8 mm) observation wells can be installed within the hollow-stem augers. Testing of ESASS was conducted at one waste-disposal site with tetrachloroethylene (PCE) contamination and at two reference sites with no known waste-disposal history. All three sites have similar geology and are underlain by glacial, stratified-drift deposits. For the applications tested, ESASS proved to be a useful tool in vertical profiling of groundwater quality. At the waste site, PCE concentrations measured with ESASS profiling at several depths were comparable (relative percent difference <25%) to PCE concentrations sampled from wells. Vertical profiling with ESASS at the reference sites illustrated the vertical resolution achievable in the profile system; shallow groundwater quality varied by a factor of five in concentration of some constituents (nitrate and nitrite) over short (0.61 m) distances.

Ground Water Monitoring and Remediation

Groundwater geochemical and selected volatile organic compound data, Operable Unit 1, Naval Undersea Warfare Center, Division Keyport, Washington, June 2009

Previous investigations indicate that natural attenuation and biodegradation of chlorinated volatile organic compounds (VOCs) are substantial in groundwater beneath the 9-acre former landfill at Operable Unit 1 (OU 1), Naval Undersea Warfare Center, Division Keyport, Washington. Phytoremediation combined with ongoing natural attenuation processes was the preferred remedy selected by the U.S. Navy, as specified in the Record of Decision for the site. The U.S. Navy planted two hybrid poplar plantations on the landfill in spring 1999 to remove and to control the migration of chlorinated VOCs in shallow groundwater. The U.S. Geological Survey (USGS) has continued to monitor groundwater geochemistry to ensure that conditions remain favorable for contaminant biodegradation as specified in the Record of Decision. This report presents groundwater geochemical and selected VOC data collected at OU 1 by the USGS during June 15-17, 2009, in support of long-term monitoring for natural attenuation. For 2009, groundwater samples were collected from 13 wells and 9 piezometers. Samples from all wells and piezometers were analyzed for redox sensitive constituents, and samples from 10 of 18 upper-aquifer wells and piezometers and 3 of 4 intermediate-aquifer wells also were analyzed for chlorinated VOCs. Concentrations of redox sensitive constituents measured in 2009 were consistent with previous years, with dissolved hydrogen (H2) concentrations ranging from less than 0.1 to 1.8 nanomolar (nM), dissolved oxygen concentrations all at 0.6 milligram per liter or less; little to no detectable nitrate; abundant dissolved manganese, iron, and methane; and commonly detected sulfide. The reductive declorination byproducts-methane, ethane, and ethene-were not detected in samples collected from the upgradient wells in the landfill or the upper aquifer beneath the northern phytoremediation plantation. Chlorinated VOC concentrations in 2009 at most piezometers were similar to or slightly less than chlorinated VOC concentrations measured in previous years. In 2009, concentrations of reductive dechlorination byproducts ethane and ethene were less than those measured in 2008 at most northern plantation wells and piezometers. For the upper aquifer beneath the southern phytoremediation plantation, chlorinated VOC concentrations in 2009 at the piezometers were extremely high and continued to vary considerably over space and between years. At piezometer P1-9, the total chlorinated VOC concentration increased from 25,000 micrograms per liter in 2008 to more than 172,000 micrograms per liter in 2009. At piezometer P1-7 in 2009, the concentrations of trichloroethene and cis-1,2-dichloroethene (cis-DCE) were the highest to date. The reductive dechlorination byproducts ethane and ethene were detected at all wells and piezometers in the southern plantation with the exception of piezometer P1-8, although the measured concentrations were not consistently high. For the intermediate aquifer, concentrations of redox sensitive constituents and VOCs in 2009 at wells MW1-25, MW1-28, and MW1-39 were consistent with concentrations measured in previous years. Concentrations of the reductive dechlorination byproducts ethane and ethene at wells MW1-25 and MW1-28 were equal to or greater than previously measured concentrations.

Washington

Groundwater geochemical and selected volatile organic compound data, Operable Unit 1, Naval Undersea Warfare Center, Division Keyport, Washington, June 2011

Previous investigations indicate that concentrations of chlorinated volatile organic compounds are substantial in groundwater beneath the 9-acre former landfill at Operable Unit 1, Naval Undersea Warfare Center, Division Keyport, Washington. Phytoremediation combined with ongoing natural attenuation processes was the preferred remedy selected by the U.S. Navy, as specified in the Record of Decision for the site. The U.S. Navy planted two hybrid poplar plantations on the landfill in spring 1999 to remove and to control the migration of chlorinated volatile organic compounds in shallow groundwater. The U.S. Geological Survey has continued to monitor groundwater geochemistry to ensure that conditions remain favorable for contaminant biodegradation as specified in the Record of Decision. This report presents groundwater geochemical and selected volatile organic compound data collected at Operable Unit 1 by the U.S. Geological Survey during June 20-22, 2011, in support of long-term monitoring for natural attenuation. In 2011, groundwater samples were collected from 13 wells and 9 piezometers. Samples from all wells and piezometers were analyzed for redox sensitive constituents and dissolved gases, and samples from 5 of 13 wells and all piezometers also were analyzed for chlorinated volatile organic compounds. Concentrations of redox sensitive constituents measured in 2011 were consistent with previous years, with dissolved oxygen concentrations all at 0.4 milligram per liter or less; little to no detectable nitrate; abundant dissolved manganese, iron, and methane; and commonly detected sulfide. The reductive declorination byproducts - methane, ethane, and ethene - were either not detected in samples collected from the upgradient wells in the landfill and the upper aquifer beneath the northern phytoremediation plantation or were detected at concentrations less than those measured in 2010. Chlorinated volatile organic compound concentrations in 2011 at most piezometers were similar to or slightly less than chlorinated volatile organic compound concentrations measured in previous years. For the upper aquifer beneath the southern phytoremediation plantation, chlorinated volatile organic compound concentrations in 2011 in groundwater from the piezometers were extremely high and continued to vary considerably over space and between years. At piezometer P1-9, the total chlorinated volatile organic compound concentrations increased from 9,500 micrograms per liter in 2010 to more than 44,000 micrograms per liter in 2011. Total chlorinated volatile organic compound concentrations decreased at piezometers P1-6, P1-7, and P1-10 compared to the concentrations measured in 2010. One or both of the reductive dechlorination byproducts ethane and ethene were detected at all piezometers and three of the four wells in the southern plantation. For the intermediate aquifer, concentrations of redox sensitive constituents and chlorinated volatile organic compounds in 2011 were consistent with concentrations measured in previous years, with the exception of notable decreases in sulfate and chloride concentrations at well MW1-28. Concentrations of the reductive dechlorination byproducts ethane and ethene decreased at wells MW1-25 and MW1-28 compared to previously measured concentrations.

Washington

Analysis of factors affecting plume remediation in a sole-source aquifer system, southeastern Nassau County, New York

Several plumes of dissolved, chlorinated solvents, including trichloroethylene, have been identified in a sole-source aquifer near the former Northrop Grumman Bethpage Facility and Naval Weapons Industrial Reserve Plant sites in southeastern Nassau County, New York. Past investigations have documented that the groundwater contamination originated from this industrial area and now extends to the south, in the direction of groundwater flow. The intermixed plumes are commonly referred to as the “Navy Grumman groundwater plume.” Detailed groundwater-flow modeling was needed for the New York State Department of Environmental Conservation (NYSDEC) to evaluate design options necessary for the construction, operation, optimization, maintenance, and monitoring of a groundwater extraction and treatment cleanup plan selected in a December 2019 Amended Record of Decision by the NYSDEC to comprehensively address these plumes. Consequently, the NYSDEC began a cooperative study with the U.S. Geological Survey in 2020 to better understand the local hydrogeologic framework using two independent approaches to characterize aquifer heterogeneity and update an existing regional groundwater-flow model to provide transient boundary conditions for new inset groundwater-flow models of the plume area. We developed these detailed inset models for the two independent aquifer characterizations using history-matching techniques coupled with a novel approach to risk-based management optimization of the remedial design. We also used the updated regional model to assess this optimized groundwater extraction and treatment design for potential saltwater intrusion. The ensembles of parameters resulting from history matching provided a platform with which to evaluate capture by water-supply and remedial wells using particle-tracking techniques. Using the ensemble to select a risk stance, we performed multiobjective optimization to identify various configurations of remedial pumping that are consistent with external constraints and that favor potentially competing objectives. Multiple solutions provide tradeoffs that NYSDEC can consider. In general, pumping redistribution may help to prevent further contamination migration downgradient. These and other study results are intended to support decisions for the remedial design focused on the local area encompassing the full extent of the Navy Grumman groundwater plume.

New York

Treatability study to evaluate bioremediation of trichloroethene at Site K, former Twin Cities Army Ammunition Plant, Arden Hills, Minnesota, 2020–22

Executive Summary Chlorinated solvents, including trichloroethene (TCE) and other chlorinated volatile organic compounds (cVOCs), are widespread contaminants that can be treated by bioremediation approaches that enhance anaerobic reductive dechlorination. Reductive dechlorination can be enhanced either through the addition of an electron donor (biostimulation) or the addition of a known dechlorinating culture (bioaugmentation) along with an electron donor. Although bioremediation has been applied at many TCE-contaminated groundwater sites, application in source zones at sites where residual dense nonaqueous phase liquid (DNAPL) is present is more limited. In this study, laboratory and field treatability tests were completed to evaluate the potential application of anaerobic bioremediation for a shallow groundwater plume containing TCE in a perched alluvial aquifer at Site K, former Twin Cities Army Ammunition Plant, Arden Hills, Minnesota, which was on the National Priorities List as the New Brighton/Arden Hills Superfund site until 2019. In addition to the presence of residual DNAPL at the site, temporal variability in groundwater flow directions and input of oxygenated recharge were possible complicating factors for the application of enhanced anaerobic biodegradation in the shallow plume. The Site K plume extends beneath the footprint of Building 103, which was demolished in 2006, and soil excavations to a maximum depth of 6 feet (ft) below ground surface in 2014 were known to leave some deeper contaminated soil in place in the TCE source area. Groundwater treatment at the site, formalized as part of the 1997 Record of Decision, has been in operation since 1986 and consists of an extraction trench at the downgradient edge of the plume to collect groundwater, which is then pumped to an on-site air stripper. Groundwater concentrations in the plume have been relatively stable since treatment began, indicating a continued source of TCE in the aquifer. The desire for a destructive remedy that would enhance the removal of cVOCs in the aquifer at Site K and shorten the remediation timeframe led the U.S. Army to request that the U.S. Geological Survey conduct a groundwater treatability study to assess bioremediation. This report describes the U.S. Geological Survey bioremediation treatability study conducted during 2020–22, including pre-design site characterization to assist in formulating the bioremediation approach, laboratory experiments to support the design of the field pilot test, and implementation and 1-year performance monitoring results for the pilot test. Pre-design site characterization included the collection of soil cores for cVOC analysis and lithologic descriptions and the re-installment of three wells to obtain hydrologic measurements and initial groundwater chemistry. Relatively flat head gradients were measured at the site, and substantial decreases in water-level elevations occurred from spring to summer (May–July 2021). Continuous water-level monitoring indicated a rapid response to precipitation. Groundwater flow velocities were consistently less than 0.5 foot per day, and the pilot bioremediation test was therefore designed with short lateral distances (about 5 ft) between injection and individual monitoring points. Soil analyses confirmed that high volatile organic compound contamination was left in place in the source area. The highest concentrations were near or in clay at the base of the perched aquifer. Concentrations of cVOCs measured in the replaced wells were consistent with historical data and had a maximum TCE concentration of 57,700 micrograms per liter (μg/L), indicative of nearby residual DNAPL based on the general rule of observed concentrations exceeding 1 percent of solubility. The primary TCE daughter product detected was 1,2-cis-dichloroethene (cisDCE), which indicated limited reductive dechlorination in the plume. Groundwater in both the source and downgradient areas was relatively reducing during the pre-design characterization, particularly in the source area where methane concentrations greater than 400 μg/L were measured. Initial laboratory tests conducted using native aquifer microorganisms from the three replacement wells showed that anaerobic TCE biodegradation rates were low when biostimulated with the addition of sodium lactate as an electron donor, also known as a carbon donor, and resulted in the production of only cisDCE. Addition of a known dechlorinating culture, WBC-2, however, resulted in rapid biodegradation and production of ethene, verifying complete reductive dechlorination of TCE. Microcosms constructed with aquifer soil collected from the site were used to evaluate other electron donors besides lactate to support reductive dechlorination by WBC-2, including corn syrup as an alternative fast-release compound and whey, soy-based vegetable oil, and 3-D Microemulsion (Regenesis, San Clemente, California) as slow-release compounds. First-order rate constants for total organic chlorine removal in these WBC-2 amended microcosms were greatest with either lactate or vegetable oil as the donor, ranging between 0.061 and 0.047 per day or corresponding half-lives of 11–15 days. Testing of commercial products in other WBC-2-bioaugmented microcosms led to selection for the field pilot test of an emulsified vegetable oil product that also contained some sodium lactate as a fast-release donor. Delaying the addition of WBC-2 relative to the donor in the microcosms resulted in the most rapid overall biodegradation rates. The selected design for the pilot test utilized three separate test plots, each about 30-ft wide and 60-ft long: plots GS1 and GS2 in the source area of the plume and plot GS3 in the downgradient area of the plume near the excavation trench. Each test plot had one injection well, one monitoring well upgradient from the injection point, and 12 surrounding monitoring wells in a grid to capture variable groundwater flow directions. Donor injections, which included a bromide tracer, were completed in October 2021, immediately following baseline sampling, and the WBC-2 culture was injected about 40 days later, between November 30 and December 2, 2021. Performance monitoring conducted until December 2022 included hydrologic measurements and analyses of cVOCs, redox-sensitive constituents, dissolved organic carbon, bromide, volatile fatty acids, compound-specific carbon isotopes, and microbial communities. The biogeochemical data collected during the pilot tests in the three treatment plots showed that enhanced, complete reductive dechlorination of cVOCs in the groundwater was achieved in the GS1 and GS3 plots. In contrast, evidence of distribution of the injected amendments and subsequent biodegradation was limited in GS2, which was in an area of more heterogeneous soil lithology and low water table elevations. The molar composition of volatile organic compounds in the GS1 and GS3 plots was dominated by ethene in wells that were reached by the injected amendments by the end of the monitoring period. In the GS1 and GS3 plots, similar patterns were observed of cVOC concentrations decreasing to near detection levels, or below, at some wells sampled in July and October 2022, whereas ethene became dominant and indicated sustained complete reductive dechlorination. Baseline cVOC concentrations were more than a factor of 10 higher in the groundwater in the GS1 plot than in GS3, but no apparent inhibition of complete dechlorination occurred. As expected from the initial pre-design site data and the laboratory experiments, enhanced dissolution of residual DNAPL coupled to biodegradation was evident in the GS1 plot, where a marked increase in dichloroethene (DCE) above the initial baseline and upgradient TCE and DCE concentrations occurred. DCE concentrations subsequently declined where DNAPL dissolution was evident, concurrent with production of vinyl chloride and then predominantly ethene. Thus, overall biodegradation rates outpaced the DNAPL dissolution and desorption and DCE production in the source area. This success in complete degradation to predominantly ethene was achieved even in areas where the DCE concentrations reached a maximum of about 30,000 μg/L. Compound specific isotope analysis of carbon in TCE, cisDCE, trans-1,2-dichloroethene, and vinyl chloride was conducted to provide another line of evidence of the occurrence and extent of anaerobic biodegradation. Along a flow path in each plot that was affected by the injected amendments, carbon isotopes in the TCE and daughter cVOCs in the groundwater became isotopically heavier, indicating biodegradation. Enhanced biodegradation rates calculated from the field tests in GS1 and GS3 showed half-lives of 36.9–75.3 days for DCE degradation and 9.48–38.5 days for ethene production. Notably, these ethene production rates calculated from the field tests are consistent with the results of WBC-2-bioaugmented microcosms amended with either lactate or vegetable oil, which had half-lives for total organic chlorine removal that ranged from 11 to 15 days. These rates indicated rapid enhanced biodegradation, which is promising for application of a full-scale bioremediation remedy. Ultimately, however, the mass of residual or sorbed TCE in the aquifer that remains accessible for dissolution and biodegradation would likely control the time required for a full-scale bioremediation effort to achieve performance goals for TCE and cisDCE specified in the Record of Decision for Site K. The field pilot tests showed that the relatively low hydraulic head gradients and temporal changes in groundwater flow directions in the shallow aquifer would add complexity to a full-scale bioremediation effort. The radius of influence (ROI) at GS1 and GS3 (16.3 ft and 12.7 ft, respectively) were close to the design ROI of 15 ft. The estimated ROI at GS2 was about four times the design ROI, but may be less reliable at this location owing to groundwater flow direction. In addition, the low temperatures following WBC-2 injection in late November to early December 2021, in combination with the low hydraulic head gradients, were probably major factors in the delay observed before the onset of enhanced biodegradation following injection of the culture. Additional test injections could be beneficial to optimize the timing of donor and culture injections with the variable temperatures and hydraulic head in the shallow aquifer.

Minnesota

Preliminary investigation of soil and ground-water contamination at a U.S. Army Petroleum Training Facility, Fort Lee, Virginia, September-October 1989

Fuel-oil constituents in the soil and groundwater at the Fort Lee Petroleum Training Facility near Petersburg, Virginia, were studied by the U.S. Geological Survey (USGS) in cooperation with the Department of Defense, U.S. Army. The study included installation of 25 groundwater monitoring wells and description of groundwater flow patterns of the shallow-aquifer system underlying the facility. Soil and groundwater samples were collected to determine the concentrations of fuel-oil constituents and to determine the potential for off-site migration of the constituents. Total petroleum hydrocarbon concentrations up to 18,400 mg/km were reported in soil samples. Concentrations of benzene in water from wells at the facility were up to 130 micrograms per liter (ug/L), and concentrations of ethylbenzene and xylene were up to 54 and 120 ug/L, respectively. Potential exists for off-site migration of the contaminants and migration of contaminants downward to deeper aquifers. Further investigations of these potential contamination-migration pathways are warranted. Risk identification at the Petroleum Training Facility cannot be properly addressed because the distribution of the fuel-oil constituents has not been fully characterized. Preliminary identification of risk, however is presented by an examination of toxicity data for the chemical constituents reported in the groundwater at the facility. Concentrations of constituents were compared to the maximum contaminant levels (MCLs) for drinking water established by the U.S. Environmental Protection Agency (USEPA). Concentrations of benzene in water from wells at the facility exceed the USEPA 's 5 ug/L MCL by as much as 26 times. Sufficient data are not available to fully design the remedial-action plan for the facility; however, general responses to contamination of the type associated with the facility include no-action, monitoring, institutional controls, removal, and treatment.

Virginia

Numerical modeling of groundwater flow in the crystalline-rock aquifer in the vicinity of the Savage Municipal Water-Supply Well Superfund site, Milford, New Hampshire

In 2010, tetrachloroethylene (PCE), a chlorinated volatile organic compound, was detected in groundwater from deep (more than 300 feet below land surface) fractures in monitoring wells tapping a crystalline-rock aquifer. The aquifer underlies the Milford-Souhegan glacial-drift aquifer, a high water-producing aquifer, and the Savage Municipal Water-Supply Well Superfund site in Milford, New Hampshire. Between 30 and 40 residential water-supply wells are near (0.25 mile north of) the PCE-contaminated monitoring wells. Some of the residential water-supply wells are likely installed in similar rock types and formations as those of the monitoring wells installed as part of the Superfund site. As of 2020, periodic sampling by the U.S. Environmental Protection Agency and New Hampshire Department of Environmental Services (cooperative partners for this study) since 1996 had not detected PCE in groundwater from the residential water-supply wells. Nevertheless, understanding the vulnerability of the residential water wells to capture PCE contaminated groundwater was of concern. A numerical groundwater flow model was developed by the U.S. Geological Survey to assess groundwater flow and advective transport of PCE-contaminated groundwater in the crystalline-rock aquifer of the Milford area. The model (called the area-wide model) encompasses a 26.5-square mile area to allow for more accurate computation of water fluxes near the PCE-contaminated monitoring wells and the residential water wells. Simulations with the area-wide model show that, with the 2016 configuration of residential wells, capture of PCE by the residential water wells appears unlikely for hydrologic conditions typical of 2010 based on steady-state, advective transport modeling. However, simulations also show that adding residential water wells to the north of the PCE-contaminated monitoring wells could affect the transport of PCE. Groundwater withdrawals at other adjacent wells in the overlying Milford-Souhegan glacial-drift aquifer affect advective transport in the crystalline-rock aquifer. Therefore, the potential for future changes in withdrawals in the area, as well as changes in hydrologic conditions, including groundwater recharge and streamflow amounts, should be considered in the remedial assessment process. The development of the area-wide model and linkages established by this study with previously developed Milford-Souhegan glacial-drift aquifer transport models will help facilitate the development of remedial strategies for this Superfund site.

New Hampshire

Time-domain electromagnetic soundings and passive-seismic measurements for delineation of saline groundwater in the Genesee Valley-fill aquifer system, western New York, 2016–17

The U.S. Geological Survey, in cooperation with the New York State Department of Environmental Conservation, used noninvasive surface geophysics in the investigation of the distribution of saline groundwater in the valley-fill aquifer system of the Genesee River Valley near the former Retsof salt mine in western New York. In 1994, the Retsof salt mine, the largest of its kind in the western hemisphere, underwent a catastrophic roof collapse that resulted in groundwater inflow from the valley-fill aquifer system and bedrock fracture zones into the mine through two bedrock-rubble chimneys and the subsequent dissolution and filling of the mine with saturated brine. Since the early 2000s, except for a period of remedial pumping in 2006 to 2013, high-salinity water has migrated upward through the rubble chimneys into the basal part the aquifer system. The extent of saline-water migration within the aquifer system had not been evaluated since the end of remedial pumping when all the monitoring wells were grouted shut and abandoned. Installation of a monitoring-well network would be expensive and difficult given the thickness and heterogeneous character of valley fill. An investigation of the current extent of saline water in the aquifer system was warranted because the basal part of the aquifer is shallow to the north and it is used for water supply. In fall 2016 and fall 2017, the U.S. Geological Survey collected time-domain electromagnetic soundings at 105 sites along 13 cross-valley transects north and south of the mine-collapse area, east of Piffard, and on the Fowlerville Moraine. The time-domain electromagnetic soundings were colocated with passive-seismic measurements to estimate the bedrock-surface elevation through use of a regression equation developed from measurements at well sites with reported bedrock depths in the study area. An integrated analysis of the time-domain electromagnetic soundings with the depth-to-bedrock estimates, well logs, and past chloride-monitoring data suggests the presence of a zone of high electrical conductivity associated with saline water in the confined lower part of the valley-fill aquifer system. This high-salinity zone delineated in the lower confined aquifer extends from the mine-collapse area northward for more than 2.5 miles (4.0 kilometers). The chloride concentration in groundwater within this high-conductivity zone may be about 20,000 milligrams per liter. Saline water flowing upward through the bedrock-rubble chimneys and mixing with northward groundwater flow in the lower confined aquifer likely is a major source of chlorides for this high-conductivity zone. The northern extent of the zone is unclear because of the presence of highly saline water zones that were delineated by time-domain electromagnetic soundings in the lower confined aquifer and uppermost bedrock and are probably associated with historic salt-solution wells in Piffard or possibly sourced from natural brine pools.

New York

A conceptual site model of contaminant transport pathways from the Bremerton Naval Complex to Sinclair Inlet, Washington, 2011–21

Historical activities on the Bremerton Naval Complex (BNC) in Puget Sound, Washington, have resulted in Sinclair Inlet sediments with elevated concentrations of contaminants, including organic contaminants such as polychlorinated biphenyls and trace elements including mercury. Six U.S. Geological Survey–U.S. Navy datasets have been collected since the last major assessment, in 2013, of soil and groundwater contaminant transport pathways and mercury loading estimates from the BNC to Sinclair Inlet. These include: mercury isotope analysis to support sourcing of mercury in Sinclair Inlet; mercury sampling within the dry dock systems; nearshore thermal surveys to identify potential groundwater discharge locations to Sinclair Inlet; time-series monitoring in nearshore wells to understand the inland extent and dynamics of the tidal mixing zone; tidal studies of mercury in nearshore monitoring wells in an area of contaminated fill material called Site 1; and a spatial survey of trace elements and other parameters in nearshore monitoring wells, pore water, seeps, surface water, and sediment along unwalled shorelines in the western part of the BNC. The results were incorporated into an updated Conceptual Site Model and used to update contaminant load estimates from the terrestrial BNC to Sinclair Inlet. The results from these studies provide data to the U.S. Navy to support prioritization of on-going remediation actions to manage contamination on the BNC that reduce potential impacts to Sinclair Inlet sediment, surface water, and fish and shellfish tissue. Mercury isotope analysis of surface sediments and particulate material indicated that a similar industrial mercury profile is present throughout Puget Sound, including terrestrial and marine BNC samples and in other Sinclair Inlet sediments and persists across regions with low and elevated mercury concentrations. Two sources of mercury at the BNC are Sites 1 and 2 subsurface soils/fill material, with total mercury concentrations in particulates collected from the bottom of monitoring wells drilled in these materials ranging from 18,000 to 44,000 nanograms per gram (as compared to the Washington State Marine Sediment Cleanup Screening Level of 590 nanograms per gram). Contaminants are transported from the terrestrial BNC to Sinclair Inlet via three primary pathways, (1) stormwater outfalls, (2) dry dock discharges, and (3) direct discharge along unwalled shorelines. Previous loading estimates (based on filtered total mercury) ranked stormwater outfalls, particularly outfall PSNS015 in Site 2 soils, as the largest soil and groundwater contaminant transport pathway from the terrestrial BNC to Sinclair Inlet. Updated loading estimates in this report suggest that the dry dock systems may be a larger pathway of mercury from the terrestrial BNC to Sinclair Inlet than previously thought, within the same order of magnitude as the PSNS015 storm-drain system. Trace-element loads via direct shoreline discharge are difficult to estimate due to the large and dynamic tidal mixing zone of groundwater and seawater in the nearshore along unwalled shorelines. However, current best estimated ranges suggest that direct shoreline discharge is one of the three main pathways and may contribute smaller mercury loads than the stormwater and the dry dock systems. Along unwalled shorelines, direct groundwater discharge of terrestrial contaminants may be less important than recirculating seawater in the nearshore mixing zone that can extract contaminants from nearshore subsurface material. Total estimated mercury loads from the terrestrial BNC to Sinclair Inlet range from approximately 40 to 200 grams of filtered total mercury per year and a minimum of 70–350 grams of particulate total mercury per year, for a minimum total of 110–525 grams of whole (filtered plus particulate) total mercury per year. Data gaps are identified that, if filled, would further refine the Conceptual Site Model and contaminant loading estimates from the terrestrial BNC to Sinclair Inlet.

Washington