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At least 19 recordsLinked to original sources
USGS2007

Demonstration and validation of a regenerated cellulose dialysis membrane diffusion sampler for monitoring ground-water quality and remediation progress at DoD sites (ER-0313)

This final technical report documents the demonstration and validation of regenerated cellulose dialysis membrane diffusion samplers for use in collecting ground water samples for a range of inorganic and organic water-quality parameters. This project, ER-0313, was funded by the Environmental Security Technology Certification Program (ESTCP). The primary objectives of the project were; (1) to determine the usefulness of dialysis samplers in collecting a range of organic and inorganic water quality constituents from ground water, (2) to determine the optimum equilibration times for these constituents to diffuse into the dialysis sampler, (3) to compare water quality results and sampling costs from samples collected with dialysis samplers to samples collected with a low-flow purging technique and polyethylene diffusion bag (PDB) samplers, and (4) to transfer the technology while gaining regulatory acceptance. Field comparisons were conducted at three Department of Defense (DoD) sites: (1) Naval Air Engineering Station (NAES) Lakehurst, NJ, (2) Naval Base Ventura County (NBVC), Port Hueneme and Pt. Mugu, CA, and (3) Naval Air Warfare Center (NAWC) West Trenton, NJ. Dialysis samplers were found to cost significantly less than samples collected with a low-flow purging procedure. Field sampling time was reduced by a factor of more than six times, compared to low-flow purging. The total sampling costs per sample was estimated to be three times less, compared to low-flow purging.

Technical Report↗
USGS2006

Use of plume mapping data to estimate chlorinated solvent mass loss

Results from a plume mapping study from November 2000 through February 2001 in the sand-and-gravel surficial aquifer at Dover Air Force Base, Delaware, were used to assess the occurrence and extent of chlorinated solvent mass loss by calculating mass fluxes across two transverse cross sections and by observing changes in concentration ratios and mole fractions along a longitudinal cross section through the core of the plume. The plume mapping investigation was conducted to determine the spatial distribution of chlorinated solvents migrating from former waste disposal sites. Vertical contaminant concentration profiles were obtained with a direct-push drill rig and multilevel piezometers. These samples were supplemented with additional ground water samples collected with a minipiezometer from the bed of a perennial stream downgradient of the source areas. Results from the field program show that the plume, consisting mainly of tetrachloroethylene (PCE), trichloroethene (TCE), and cis-1,2-dichloroethene (cis-1,2-DCE), was approximately 670 m in length and 120 m in width, extended across much of the 9- to 18-m thickness of the surficial aquifer, and discharged to the stream in some areas. The analyses of the plume mapping data show that losses of the parent compounds, PCE and TCE, were negligible downgradient of the source. In contrast, losses of cis-1,2-DCE, a daughter compound, were observed in this plume. These losses very likely resulted from biodegradation, but the specific reaction mechanism could not be identified. This study demonstrates that plume mapping data can be used to estimate the occurrence and extent of chlorinated solvent mass loss from biodegradation and assess the effectiveness of natural attenuation as a remedial measure.

Ground Water Monitoring and Remediation↗
USGS2007

A field test of electromigration as a method for remediating sulfate from shallow ground water

Eloctromigraiion offers a potential tool for remediating ground water contaminated with highly soluble components, such as Na + , Cl, NO 3 and SO 4 − . A field experiment was designed to lest the efficacy of electromigration for preconcontrating dissolved SO 4 2 in ground water associated with a fossil-fuel power plant. Two shallow wells, 25 feel apart (one 25 feel deep, the other 47 feet deep), were constructed in the upper portion of an unconfined alluvial aquifer. The wells were constructed with a double-wall design, with an outer casing of 4-inch PVC and an inner lube of 2-inch FVC; both were fully slotted (0.01 inch). Electrodes were constructed by wrapping the inner lulling with a 100-foot length of rare-earth metal oxide/copper wire. An electrical potential of 10.65 volts DC Was applied, and tests were run for periods of 12, 44, and 216 hours. Results showed large changes in the pH from the initial pH of ground water of about 7.5 to values of approximately 2 and 12 at the anode and cathode, respectively. Despite the fact that the test conditions were far from ideal, dissolved SO 4 2- ; was significantly concentrated at the anode. Over a period of approximately nine days, the concentration of SO 4 2- at the anode reached what appeared to he a steady-state value of 2200 mg/L. compared lo the initial value in ground water of approximately 1150 mg/L. The results of this field lest should encourage further investigation of electromigration as a tool in the remediation of contaminated ground water.

Ground Water Monitoring and Remediation↗
USGS2011

Reinterpreting the importance of oxygen-based biodegradation in chloroethene-contaminated groundwater

Chlororespiration is common in shallow aquifer systems under conditions nominally identified as anoxic. Consequently, chlororespiration is a key component of remediation at many chloroethene-contaminated sites. In some instances, limited accumulation of reductive dechlorination daughter products is interpreted as evidence that natural attenuation is not adequate for site remediation. This conclusion is justified when evidence for parent compound (tetrachloroethene, PCE, or trichloroethene, TCE) degradation is lacking. For many chloroethene-contaminated shallow aquifer systems, however, nonconservative losses of the parent compounds are clear but the mass balance between parent compound attenuation and accumulation of reductive dechlorination daughter products is incomplete. Incomplete mass balance indicates a failure to account for important contaminant attenuation mechanisms and is consistent with contaminant degradation to nondiagnostic mineralization products like CO 2 . While anoxic mineralization of chloroethene compounds has been proposed previously, recent results suggest that oxygen-based mineralization of chloroethenes also can be significant at dissolved oxygen concentrations below the currently accepted field standard for nominally anoxic conditions. Thus, reassessment of the role and potential importance of low concentrations of oxygen in chloroethene biodegradation are needed, because mischaracterization of operant biodegradation processes can lead to expensive and ineffective remedial actions. A modified interpretive framework is provided for assessing the potential for chloroethene biodegradation under different redox conditions and the probable role of oxygen in chloroethene biodegradation.

Ground Water Monitoring and Remediation↗
USGS2010

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↗
USGS2019

Examining the extraction efficiency of petroleum-derived dissolved organic matter in contaminated groundwater plumes

The extraction efficiency of petroleum-derived dissolved organic matter (DOM) was examined for groundwater samples from an aquifer contaminated with crude oil. Four different types of extraction were used to determine which method is best suited for the analysis of potentially toxic petroleum-derived DOM. The four types were a liquid-liquid extraction (LLE) with dichloromethane (EPA method 3510C), and three solid-phase extraction (SPE) stationary phases that are routinely used for extraction of polar analytes from water. For the LLE, that is selective for non-polar compounds, the extraction efficiency of petroleum-derived DOM decreased downgradient as the petroleum-derived DOM becomes increasingly polar due to biodegradation. In contrast, the average extraction efficiency by the SPE methods was greater than 65 % across the gradient. The results showed that SPE is more efficient for extracting petroleum-derived DOM at hydrocarbon-contaminated sites. The use of a method with greater extraction efficiency for partially-oxidized hydrocarbons may prove useful in determining relationships between their composition and structure and potential for risks to human health or the environment.

Ground Water Monitoring and Remediation↗
USGS2022

Understanding the evolution of groundwater-contaminant plume chemistry emanating from legacy contaminant sources: An example from a long-term crude oil spill

Understanding the evolution of plumes emanating from residual hydrocarbon contaminant sources requires evaluating how changes in source compositions over time cause changes in dissolved plume chemistry as residual sources age. This study investigates such changes at the site of a 1979 crude-oil pipeline spill and is the first comprehensive look at groundwater chemistry associated with a residual hydrocarbon source zones in different stages of aging. The data show a direct relationship between concentrations of benzene and naphthalene in the residual oil and those measured in water samples collected below the oil. Groundwater associated with oil near the spill site had different chemical composition compared with water associated with oil that had spread downgradient from the spill zone, indicating a shift in biodegradation reactions. These results emphasize that source zone processes are spatially and temporally heterogeneous and should be accounted for in natural attenuation studies where residual source zones persist.

Minnesota↗
USGS2007

Installation of observation wells on hazardous waste sites in Kansas using a hollow-stem auger

Noncontaminating procedures were used during the hollow-stem auger installation of 12 observation wells on three hazardous waste sites in Kansas. Special precautions were taken to ensure that water samples were representative of the ground water in the aquifer and were not subjected to contamination from the land surface or cross contamination from within borehole. Precautions included thorough cleaning of the hollow-stem auger and casing, keeping drill cuttings from falling back into the borehole while drilling, and not adding water to the borehole. These procedures were designed to prevent contamination of the ground water during well installation. Because of the use of water during well installation could contaminate the aquifer or dilute contaminants already present in the aquifer, two methods of well installation that did not introduce outside water to the borehole were used. The first method involved using a slotted 3/4 -inch coupling that was attached to the bit plate of the hollow-stem auger, allowing formation water to enter the auger, thereby preventing sand-plug formation. This method proved to be adequate, except when drilling through clay layers, which tended to clog the slotted coupling. The second method involved screened well swab that allowed only formation water to enter the hollow-stem auger and prevented sand from plugging the hollow-stem auger when the bit plate was removed.

Ground Water Monitoring and Remediation↗
USGS2007

Effects of sample isolation and handling on the recovery of purgeable organic compounds

This report compares the recovery of purgeable organic compounds (POCs) obtained by using a downhole isobaric sampler developed by the U.S. Geological Survey, a helical-rotor submersible pump, and a point source bailer to collect and isolate samples of ground water from three wells in Now York and New Jersey: the samples contained a total of 13 PCX's delectable at concentrations ranging from 0.5 μg/L to about 400 μg/L. This report also compares the effects of sample handling, specifically the differences in PCX concentration recovery when an isobaric sample container is filled at land surface vs. when it is filled downhole. and when samples art taken using a bailer with and without a bottom-emptying device. These case studies are used to quantify the possible effects of different sample-isolation find sample-handling techniques on POC recovery. The relative effectiveness of the three devices varied by site and by compound. Overall, the POC recoveries achieved by using the helical-rotor submersible pump and the downlink isobaric sampler were not significantly different at the 95 percent confidence, level. POC recovery obtained by using the point source bailer was 11 percent lower overall. The downhole isobaric sampler results exhibited smaller coefficients of variation than did the helical-rotor submersible pump or the point-source bailer results. However, the differences between the coefficients of variation of the downhole isobaric sampler and those of the helical-rotor submersible pump were not significant at the 95 percent confidence level. The nonsignificant smaller coefficient of variation of the downhole isobaric sampler apparently resulted from two fewer sample handling steps that exposed the sample water to ambient air. An independent experiment performed with a different downhole sampler at one of the wells used in this investigation produced a similar statistical result. Also, the POC recovery obtained by pouring sample water out the lop of a point source bailer into 40-mL vials was S percent lower than that obtained by filling vials from a bailer with a bottom-emptying device.

Ground Water Monitoring and Remediation↗
USGS2007

A sample-freezing drive shoe for a wire line piston core sampler

Loss of fluids and samples during retrieval of cores of saturated, noncohesive sediments results in incorrect measures of fluid distributions and an inaccurate measure of the stratigraphic position of the sample. To reduce these errors, we developed a hollow drive shoe that freezes in place the lowest 3 inches (75 mm) of a 1.88‐inch‐diameter (48 mm), 5‐foot‐long (1.5 m) sediment sample taken using a commercial wire line piston core smapler. The end of the core is frozen by piping liquid carbon dioxide at ambient temperature through a steel tube from a bottle at the land surface to the drive shoe where it evaporates and expands, cooling the interior surface of the shoe to about ‐ 109°F (‐ 78°C). Freezing a core end takes about 10 minutes. The device was used to collect samples for a study of oil‐water‐air distributions, and for studies of water chemistry and microbial activity in unconsolidated sediments at the site of an oil spill near Bemidji, Minnesota. Before freezing was employed, samples of sandy sediments from near the water table sometimes flowed out of the core barrel as the sampler was withdrawn. Freezing the bottom of the core allowed for the retention of all material that entered the core barrel and lessened the redistribution of fluids within the core. The device is useful in the unsaturated and shallow saturated zones, but does not freeze cores well at depths greater than about 20 feet (6 m) below water, possibly because the feed tube plugs with dry ice with increased exhaust back‐pressure, or because sediment enters the annulus between the core barrel and the core barrel liner and blocks the exhaust.

Ground Water Monitoring and Remediation↗
USGS2007

Temporal changes in VOC discharge to surface water from a fractured rock aquifer during well installation and operation, Greenville, South Carolina

Analysis of the vapor in passive vapor samplers retrieved from a streambed in fractured rock terrain implied that volatile organic carbon (VOC) discharge from ground water to surface water substantially increased following installation of a contaminant recovery well using air rotary drilling. The air rotary technique forced air into the aquifer near the stream. The injection produced an upward hydraulic gradient that appears to have transported water and contaminants from deeper parts of the aquifer through fractures into shallow parts of the aquifer. Once in the shallow flow regime, the contamination was transported to the stream, where it discharged during the next several weeks following well installation. After the recovery well was activated and began continuously pumping contaminated ground water to a treatment facility, the VOC concentrations in the stream bottom passive vapor samplers decreased to below detectable concentrations, suggesting that the withdrawal had captured the contaminated ground water that previously had discharged to the stream.

South Carolina↗
USGS2007

The relative merits of monitoring and domestic wells for ground water quality investigations

The results of two studies of the effect of agricultural land use on shallow ground water quality indicate that monitoring wells may be a better choice than domestic wells for studies of pesticide occurrence or transport, or for use as early-warning indicators of potential drinking water contamination. Because domestic wells represent the used resource, and because domestic well water may be affected by historical rather than current pesticide and land- use practices, domestic wells would be the best choice for an investigation of drinking water quality. The key difference between the domestic and monitoring wells appears to be that the monitoring wells in this study were installed exclusively to sample the shallowest possible ground water. For these studies, 48 shallow domestic wells and 41 monitoring wells were located randomly within two land-use settings (row crops and orchards) in an irrigated agricultural region of eastern Washington and sampled for 145 pesticides (including nine pesticide degradates) and common water quality indicators. Constructing and sampling monitoring wells required approximately four times the resources (including manpower and materials) as locating and sampling domestic wells. Sample collection and quality assurance procedures and analytical techniques were identical except that a portable submersible pump was required for monitoring wells. In both land-use settings, no significant difference in nitrate concentration was found between well types; however, the average number of pesticides detected per well was significantly higher (p<0.05) in the monitoring wells. A greater variety of pesticides was detected in monitoring wells; many were detected only in monitoring wells. More than 60% of detections of pesticides that were found only in domestic wells were of compounds that are no longer in use. These differences in ground water quality found in this study relate to the depth of the well and are apparently related to the age of ground water in the two types of wells and the greater effects of sorption, degradation, dilution, and dispersion that accompany longer groundwater residence times. The decision to invest resources in monitoring wells should be made in light of the study objective and should consider these differences in results from the two types of wells as well as the relative costs.

Ground Water Monitoring and Remediation↗
USGS2007

Robowell: An automated process for monitoring ground water quality using established sampling protocols

Robowell is an automated process for monitoring selected ground water quality properties and constituents by pumping a well or multilevel sampler. Robowell was developed and tested to provide a cost-effective monitoring system that meets protocols expected for manual sampling. The process uses commercially available electronics, instrumentation, and hardware, so it can be configured to monitor ground water quality using the equipment, purge protocol, and monitoring well design most appropriate for the monitoring site and the contaminants of interest. A Robowell prototype was installed on a sewage treatment plant infiltration bed that overlies a well-studied unconfined sand and gravel aquifer at the Massachusetts Military Reservation, Cape Cod, Massachusetts, during a time when two distinct plumes of constituents were released. The prototype was operated from May 10 to November 13, 1996, and quality-assurance/quality-control measurements demonstrated that the data obtained by the automated method was equivalent to data obtained by manual sampling methods using the same sampling protocols. Water level, specific conductance, pH, water temperature, dissolved oxygen, and dissolved ammonium were monitored by the prototype as the wells were purged according to U.S Geological Survey (USGS) ground water sampling protocols. Remote access to the data record, via phone modem communications, indicated the arrival of each plume over a few days and the subsequent geochemical reactions over the following weeks. Real-time availability of the monitoring record provided the information needed to initiate manual sampling efforts in response to changes in measured ground water quality, which proved the method and characterized the screened portion of the plume in detail through time. The methods and the case study described are presented to document the process for future use.

Ground Water Monitoring and Remediation↗
USGS2007

Used motor oil as a source of MTBE, TAME, and BTEX to ground water

Methyl tert-butyl ether (MTBE), the widely used gasoline oxygenate, has been identified as a common ground water contaminant, and BTEX compounds (benzene, toluene, ethylbenzene, and xylenes) have long been associated with gasoline spills. Because not all instances of ground water contamination by MTBE and BTEX can be attributed to spills or leaking storage tanks, other potential sources need to be considered. In this study, used motor oil was investigated as a potential source of these contaminants. MTBE in oil was measured directly by methanol extraction and gas chromatography using a flame ionization detector (GC/FID). Water was equilibrated with oil samples and analyzed for MTBE, BTEX, and the oxygenate tert-amyl methyl ether (TAME) by purge-and-trap concentration followed by GC/FID analysis. Raoult's law was used to calculate oil-phase concentrations of MTBE, BTEX, and TAME from aqueous-phase concentrations. MTBE, TAME, and BTEX were not detected in any of five new motor oil samples, whereas these compounds were found at significant concentrations in all six samples of the used motor oil tested for MTBE and all four samples tested for TAME and BTEX. MTBE concentrations in used motor oil were on the order of 100 mg/L. TAME concentrations ranged from 2.2 to 87 mg/L. Concentrations of benzene were 29 to 66 mg/L, but those of other BTEX compounds were higher, typically 500 to 2000 mg/L.

Ground Water Monitoring and Remediation↗
USGS2007

Soil gas screening for chlorinated solvents at three contaminated karst sites in Tennessee

Soil gas was sampled using active sampling techniques and passive collectors at three sites in Tennessee to evaluate the effectiveness of these techniques for locating chlorinated solvent sources and flowpaths in karst aquifers. Actively collected soil gas samples were analyzed in the field with a portable gas chromatograph, and the passive soil gas collectors were analyzed in the lab with gas chromatography/mass spectrometry. Results of the sampling indicate that the effectiveness of both techniques is highly dependent on the distribution of the contaminants in the subsurface, the geomorphic and hydrogeologic characteristics of the site, and, in one case, on seasonal conditions. Both active and passive techniques identified areas of elevated subsurface chlorinated solvent concentrations at a landfill site where contamination remains concentrated in the regolith. Neither technique detected chlorinated solvents known to be moving in the bedrock at a manufacturing site characterized by thick regolith and an absence of surficial karst features. Passive soil gas sampling had varied success detecting flowpaths for chloroform in the bedrock at a train derailment site characterized by shallow regolith and abundant surficial karst features. At the train derailment site, delineation of the contaminant flowpath through passive soil gas sampling was stronger and more detailed under Winter conditions than summer.

Tennessee↗
USGS2007

Do pharmaceuticals, pathogens, and other organic waste water compounds persist when waste water is used for recharge?

A proof-of-concept experiment was devised to determine if pharmaceuticals and other organic waste water compounds (OWCs), as well as pathogens, found in treated effluent could be transported through a 2.4 m soil column and, thus, potentially reach ground water under recharge conditions similar to those in arid or semiarid climates. Treated effluent was applied at the top of the 2.4 m long, 32.5 cm diameter soil column over 23 days, Samples of the column inflow were collected from the effluent storage tank at the beginning (T begin ) and end (T end ) of the experiment, and a sample of the soil column drainage at the base of the column (B end ) was collected at the end of the experiment. Samples were analyzed for 131 OWCs including veterinary and human antibiotics, other prescription and nonprescription drugs, widely used household and industrial chemicals, and steroids and reproductive hormones, as well as the pathogens Salmonella and Legionella . Analytical results for the two effluent samples taken at the beginning (T begin ) and end (T end ) of the experiment indicate that the number of OWCs detected in the column inflow decreased by 25% (eight compounds) and the total concentration of OWCs decreased by 46% while the effluent was in the storage tank during the 23-day experiment. After percolating through the soil column, an additional 18 compounds detected in T end (67% of OWCs) were no longer detected in the effluent (B end ) and the total concentration of OWCs decreased by more than 70%. These compounds may have been subject to transformation (biotic and abiotic), adsorption, and (or) volatilization in the storage tank and during travel through the soil column. Eight compounds&mdash;carbamazapine; sulfamethoxazole; benzophenone; 5-methyl-1H-benzotriazole; N,N-diethyltoluamide; tributylphosphate; tri(2-chloroethyl) phosphate; and cholesterol&mdash;were detected in all three samples indicating they have the potential to reach ground water under recharge conditions similar to those in arid and semiarid climates. Results from real-time polymerase chain reactions demonstrated the presence of Legionella in all three samples. Salmonella was detected only in T begin , suggesting that the bacteria died off in the effluent storage tank over the period of the experiment. This proof-of-concept experiment demonstrates that, under recharge conditions similar to those in arid or semiarid climates, some pharmaceuticals, pathogens, and other OWCs can persist in treated effluent after soil-aquifer treatment.

Ground Water Monitoring and Remediation↗
USGS2005

Interpreting DNAPL saturations in a laboratory-scale injection using one- and two-dimensional modeling of GPR Data

Ground-penetrating radar (GPR) is used to track a dense non-aqueous phase liquid (DNAPL) injection in a laboratory sand tank. Before modeling, the GPR data provide a qualitative image of DNAPL saturation and movement. One-dimensional (1D) GPR modeling provides a quantitative interpretation of DNAPL volume within a given thickness during and after the injection. DNAPL saturation in sublayers of a specified thickness could not be quantified because calibration of the 1D GPR model is nonunique when both permittivity and depth of multiple layers are unknown. One-dimensional GPR modeling of the sand tank indicates geometric interferences in a small portion of the tank. These influences are removed from the interpretation using an alternate matching target. Two-dimensional (2D) GPR modeling provides a qualitative interpretation of the DNAPL distribution through pattern matching and tests for possible 2D influences that are not accounted for in the 1D GPR modeling. Accurate quantitative interpretation of DNAPL volumes using GPR modeling requires (1) identification of a suitable target that produces a strong reflection and is not subject to any geometric interference; (2) knowledge of the exact depth of that target; and (3) use of two-way radar-wave travel times through the medium to the target to determine the permittivity of the intervening material, which eliminates reliance on signal amplitude. With geologic conditions that are suitable for GPR surveys (i.e., shallow depths, low electrical conductivities, and a known reflective target), the procedures in this laboratory study can be adapted to a field site to delineate shallow DNAPL source zones.

Ground Water Monitoring and Remediation↗
USGS2005

Behavior of a chlorinated ethene plume following source-area treatment with Fenton's reagent

Monitoring data collected over a 6‐year period show that a plume of chlorinated ethene–contaminated ground water has contracted significantly following treatment of the contaminant source area using in situ oxidation. Prior to treatment (1998), concentrations of perchloroethene (PCE) exceeded 4500 μg/L in a contaminant source area associated with a municipal landfill in Kings Bay, Georgia. The plume emanating from this source area was characterized by vinyl chloride (VC) concentrations exceeding 800 μg/L. In situ oxidation using Fenton's reagent lowered PCE concentrations in the source area below 100 μg/L, and PCE concentrations have not rebounded above this level since treatment. In the 6 years following treatment, VC concentrations in the plume have decreased significantly. These concentration declines can be attributed to the movement of Fenton's reagent–treated water downgradient through the system, the cessation of a previously installed pump‐and‐treat system, and the significant natural attenuation capacity of this anoxic aquifer. While in situ oxidation briefly decreased the abundance and activity of microorganisms in the source area, this activity rebounded in <6 months. Nevertheless, the shift from sulfate‐reducing to Fe(III)‐reducing conditions induced by Fenton's treatment may have decreased the efficiency of reductive dechlorination in the injection zone. The results of this study indicate that source‐area removal actions, particularly when applied to ground water systems that have significant natural attenuation capacity, can be effective in decreasing the areal extent and contaminant concentrations of chlorinated ethene plumes.

Ground Water Monitoring and Remediation↗