Geology topics

Matthew D. Petkewich

Publications and source records attributed to Matthew D. Petkewich.

30 records · Page 2Linked to original sources

USGS2009

Source, Transport, and Fate of Groundwater Contamination at Site 45, 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 and the storm sewer. 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. Extensive biodegradation of the contamination takes place in the surficial aquifer; however, the biodegradation is insufficient to reduce trichloroethene to less than milligram-per-liter concentrations prior to discharging into the storm sewers. The groundwater volatile organic compounds entering the storm sewers are substantially diluted by tidal flushing upon entry and are subject to volatilization as they are transported through the storm sewer to a discharge point in a tributary to Ballast Creek. TCE concentrations of about 2-6 micrograms per liter were present in storm-sewer water near the discharge point (sampled at manhole STS26). On three out of four sampling events at manhole STS14, the storm-sewer water contained no vinyl chloride. During a time of relatively high groundwater levels, however, 20 micrograms per liter of vinyl chloride was present in STS14 storm-sewer water. Because groundwater leaks into that storm sewer and because the storm sewer upgradient from manhole STS14 is adjacent to part of the aquifer where 2,290 micrograms per liter of vinyl chloride have been detected, there is a potential for substantially increased concentrations of vinyl chloride to discharge at the storm-sewer outfall under conditions of high groundwater levels and low tidal flushing. In addition, the observation that free-phase tetrachloroethene may have entered the storm-sewer system during the 1994 discharge means that dense nonaqueous phase liquid tetrachloroethene could have leaked from various parts of the storm sewer or discharged to surface water at the storm-sewer outfall.

South Carolina↗

USGS2009

Investigation of Contaminated Groundwater at Solid Waste Management Unit 12, Naval Weapons Station Charleston, North Charleston, South Carolina, 2008

South Carolina↗

USGS2009

Simulation of Reclaimed-Water Injection and Pumping Scenarios and Particle-Tracking Analysis near Mount Pleasant, South Carolina

The effect of injecting reclaimed water into the Middendorf aquifer beneath Mount Pleasant, South Carolina, was simulated using a groundwater-flow model of the Coastal Plain Physiographic Province of South Carolina and parts of Georgia and North Carolina. Reclaimed water, also known as recycled water, is wastewater or stormwater that has been treated to an appropriate level so that the water can be reused. The scenarios were simulated to evaluate potential changes in groundwater flow and groundwater-level conditions caused by injecting reclaimed water into the Middendorf aquifer. Simulations included a Base Case and two injection scenarios. Maximum pumping rates were simulated as 6.65, 8.50, and 10.5 million gallons per day for the Base Case, Scenario 1, and Scenario 2, respectively. The Base Case simulation represents a non-injection estimate of the year 2050 groundwater levels for comparison purposes for the two injection scenarios. For Scenarios 1 and 2, the simulated injection of reclaimed water at 3 million gallons per day begins in 2012 and continues through 2050. The flow paths and time of travel for the injected reclaimed water were simulated using particle-tracking analysis. The simulations indicated a general decline of groundwater altitudes in the Middendorf aquifer in the Mount Pleasant, South Carolina, area between 2004 and 2050 for the Base Case and two injection scenarios. For the Base Case, groundwater altitudes generally declined about 90 feet from the 2004 groundwater levels. For Scenarios 1 and 2, although groundwater altitudes initially increased in the Mount Pleasant area because of the simulated injection, these higher groundwater levels declined as Mount Pleasant Waterworks pumping increased over time. When compared to the Base Case simulation, 2050 groundwater altitudes for Scenario 1 are between 15 feet lower to 23 feet higher for production wells, between 41 and 77 feet higher for the injection wells, and between 9 and 23 feet higher for observation wells in the Mount Pleasant area. When compared to the Base Case simulation, 2050 groundwater altitudes for Scenario 2 are between 2 and 106 feet lower for production wells and observation wells and between 11 and 27 feet higher for the injection wells in the Mount Pleasant area. Water budgets for the model area immediately surrounding the Mount Pleasant area were calculated for 2011 and for 2050. The largest flow component for the 2050 water budget in the Mount Pleasant area is discharge through wells at rates between 7.1 and 10.9 million gallons of water per day. This groundwater is replaced predominantly by between 6.0 and 7.8 million gallons per day of lateral groundwater flow within the Middendorf aquifer for the Base Case and two scenarios and through reclaimed-water injection of 3 million gallons per day for Scenarios 1 and 2. In addition, between 175,000 and 319,000 gallons of groundwater are removed from this area per day because of the regional hydraulic gradient. Additional sources of water to this area are groundwater storage releases at rates between 86,800 and 116,000 gallons per day and vertical flow from over- and underlying confining units at rates between 69,100 and 150,000 gallons per day. Reclaimed water injected into the Middendorf aquifer at three hypothetical injection wells moved to the Mount Pleasant Waterworks production wells in 18 to 256 years as indicated by particle-tracking simulations. Time of travel varied from 18 to 179 years for simulated conditions of 20 percent uniform aquifer porosity and between 25 to 256 years for 30 percent uniform aquifer porosity.

South Carolina↗

USGS2008

Investigation of Contaminated Ground Water at Solid Waste Management Unit 12, Naval Weapons Station Charleston, North Charleston, South Carolina, 2006-2007

The U.S. Geological Survey investigated natural and engineered remediation of chlorinated volatile organic compound (VOC) ground-water contamination at Solid Waste Management Unit 12 at the Naval Weapons Station Charleston, North Charleston, South Carolina, beginning in 2000. The primary contaminants of interest in the study are tetrachloroethene, 1,1,1-trichloroethane, trichloroethene, cis-1,2-dichloroethene, vinyl chloride, 1,1-dichloroethane, and 1,1-dichloroethene. The permeable reactive barrier (PRB) along the main axis of the contaminant plume appears to be actively removing contamination. In contrast to the central area of the PRB, the data from the southern end of the PRB indicate that contaminants are moving around the PRB. Concentrations in wells 12MW-10S and 12MW-03S, upgradient from the PRB, showed a general decrease in VOC concentrations. VOC concentrations in some wells in the forest showed a sharp increase, followed by a decrease. In 2007, the VOC concentrations began to increase in well 12MW-12S, downgradient from the PRB and thought to be unaffected by the PRB. The VOC-concentration changes in the forest, such as at well 12MW-12S, may represent lateral shifting of the plume in response to changes in ground-water-flow direction or may represent movement of a contamination pulse through the forest.

South Carolina↗

USGS2007

Investigation of Ground-Water Contamination at Solid Waste Management Unit 12, Naval Weapons Station Charleston, North Charleston, South Carolina

The U.S. Geological Survey and the Naval Facilities Engineering Command Southeast investigated natural and engineered remediation of chlorinated volatile organic compound ground-water contamination at Solid Waste Management Unit 12 at the Naval Weapons Station Charleston, North Charleston, South Carolina. The primary contaminants of interest are tetrachloroethene, 1,1,1-trichloroethane, trichloroethene, cis-1,2-dichloroethene, vinyl chloride, 1,1-dichloroethane, and 1,1-dichloroethene. In general, the hydrogeology of Solid Waste Management Unit 12 consists of a surficial aquifer, composed of sand to clayey sand, overlain by dense clay that extends from about land surface to a depth of about 8 to 10 feet and substantially limits local recharge. During some months in the summer, evapotranspiration and limited local recharge result in ground-water level depressions in the forested area near wells 12MW-12S and 12MW-17S, seasonally reflecting the effects of evapotranspiration. Changes in surface-water levels following Hurricane Gaston in 2004 resulted in a substantial change in the ground-water levels at the site that, in turn, may have caused lateral shifting of the contaminant plume. Hydraulic conductivity, determined by slug tests, is higher along the axis of the plume in the downgradient part of the forests than adjacent to the plume, implying that there is some degree of lithologic control on the plume location. Hydraulic conductivity, hydraulic gradient, sulfur-hexafluoride measurements, and historical data indicate that ground-water flow rates are substantially slower in the forested area relative to upgradient areas. The ground-water contamination, consisting of chlorinated volatile organic compounds, extends eastward in the surficial aquifer from the probable source area near a former underground storage tank. Engineered remediation approaches include a permeable reactive barrier and phytoremediation. The central part of the permeable reactive barrier along the main axis of the contaminant plume appears to be actively removing contamination; however, ground-water contamination is moving around the southern end of the permeable reactive barrier. Changes in the contaminant concentrations along the path of ground-water transport reflect a complex variety of influences. Potential influences include dechlorination, sorption and desorption, transpirative removal by trees, lateral shifting of the plume, and the presence of zones of differing concentrations possibly reflecting one or more pulse releases of contamination from the source area. Near the source area at well 12MW-10S, volatile organic compound concentrations of cis-1,2-dichlorothene, vinyl chloride, 1,1-dichloroethane, and 1,1,1-trichloroethane continued an irregular decline, while tetrachloroethene and 1,1-dichloroethene showed marked fluctuations in concentration during 2005 and 2006. Volatile organic compound concentrations at well 12MW-03S continued to show decreasing concentrations with the June 2006 concentrations being the lowest yet recorded at that well for several volatile organic compounds. Concentration and delta carbon 13 data indicate that in the upgradient part of the plume, tetrachloroethene is being degraded to trichloroethene, which is being degraded to cis-1,2-dichloroethene, and cis-1,2-dichloroethene is accumulating faster than it is being depleted. Ground-water volatile organic compound concentrations also changed in some wells in the forested area in the midpart of the plume. Increasing tetrachloroethene and decreasing trichloroethene and 1,1-dichloroethene concentrations were observed at wells 12MW-05S and 12MW-29S, possibly reflecting a lateral shift in the axis of the contamination plume or an advancing contamination pulse. Substantial decreases in contamination occur in the forested area downgradient from well 12MW-05S. Probable major loss mechanisms in this area include evapotranspiration and sorption.

North Carolina, South Carolina↗

USGS2007

Hydrogeology and simulation of ground-water flow near Mount Pleasant, South Carolina: Predevelopment, 2004, and predicted scenarios for 2030

Heavy water use from the Cretaceous Middendorf aquifer in South Carolina has created a large, regional cone of depression in the potentiometric surface of the Middendorf aquifer in Charleston and Berkeley Counties, South Carolina. Water-level declines of up to 249 feet have been observed in wells over the past 125 years and are a result of ground-water use for public-water supply, irrigation, and private industry. To address the concerns of users of the Middendorf aquifer, the U.S. Geological Survey, in cooperation with Mount Pleasant Waterworks, updated an existing ground-water flow model to incorporate additional data that have been compiled since 1989. The updated ground-water flow model incorporates water-level data collected from 349 wells in 2004, baseflow data measured at 17 streams, hydraulic property data from 265 wells, and water-use data compiled for more than 2,700 wells for the period between the early 1900s to 2004. The ground-water flow system of the Coastal Plain physiographic province of South Carolina and parts of Georgia and North Carolina was simulated using the U.S. Geological Survey finite-difference code MODFLOW-2000. The model was vertically discretized into nine layers to include the five aquifers of the surficial, the combined Floridan aquifer system and Tertiary sand aquifer, Black Creek, Middendorf, and Cape Fear, separated by four intervening confining units. Specified-head boundary conditions were used at the lateral boundaries of the model and for the lower Coastal Plain part of the surficial aquifer; no-flow boundary conditions were used at the updip and downdip extent of the model layers and at the base of the Cape Fear aquifer. Ground-water conditions for predevelopment and 2004 were simulated using steady-state and transient approximations, respectively. Simulated water levels generally matched the observed conditions, plus or minus a 20-foot calibration target, with 56.4 and 64.8 percent of the simulated values approximating the measured values for predevelopment and 2004 hydrologic conditions, respectively. The root-mean-square error of the water-level residuals for the various model layers varied between 20.2 and 34.4 feet for predevelopment and 18.2 and 36.7 feet for 2004. The general goodness of fit also was apparent in the calculation of the ratio of standard deviation of residuals to range of observations for each modeled aquifer layer. The calculated ratios for the predevelopment and 2004 hydrologic conditions were less than 0.10 for all model layers except for the Cape Fear aquifer in both predevelopment and 2004 simulations. The Mount Pleasant model was most sensitive to changes in simulated specific storage of most model layers, vertical anisotropy of the confining units above and below the Middendorf aquifer, hydraulic conductivity of the confining units, and the specified-head boundary conditions for the surficial aquifer. The model also is sensitive to horizontal hydraulic conductivity of the Floridan aquifer system and Tertiary sand aquifer and the Black Creek and Middendorf aquifers. Simulated water budgets indicate that the primary sources of water to the model are recharge and the specified-head boundaries in layers 1 and 3. More than 88 percent of the water that discharges from the model discharges from layers 1-3 through specified-head boundaries and rivers. Approximately 11 percent of the water budget was discharged through wells for the 2004 budget. In 2004, 8.11 million gallons of water per day was discharged from wells in the Mount Pleasant area. Water to these wells is provided predominantly by lateral flow within the Middendorf aquifer. Additional water is provided from aquifer storage and leakage from confining units located above and below the Middendorf aquifer. Downward flow through the Middendorf confining unit is a reversal of the predevelopment flow direction. Five predictive water-management scenarios were simulated to determine the effects on the

South Carolina↗

USGS2005

Hydrogeology, water quality, and water-supply potential of the Lower Floridan Aquifer, coastal Georgia, 1999-2002

The hydrogeology and water quality of the upper permeable and Fernandina permeable zones of the Lower Floridan aquifer were studied at seven sites in the 24-county study area encompassed by the Georgia Coastal Sound Science Initiative. Although substantially less than the Upper Floridan aquifer in coastal Georgia, transmissivities for the Lower Floridan aquifer are in the same range as other water-supply aquifers in Georgia and South Carolina and could meet the needs of public drinking-water supply. Water of the upper permeable zone of the Lower Floridan aquifer exceeds the Federal secondary drinking-water standards for sulfate and total dissolved solids at most coastal Georgia sites and the Federal secondary drinking-water standard for chloride at the Shellman Bluff site. The top of the Lower Floridan aquifer correlates within 50 feet of the previously reported top, except at the St Simons Island site where the top is more than 80 feet higher. Based on the hydrogeologic characteristics, the seven sites are divided into the northern sites at Shellman Bluff, Richmond Hill, Pembroke, and Pineora; and southern sites at St Marys, Brunswick, and St Simons Island. At the northern sites, the Lower Floridan aquifer does not include the Fernandina permeable zone, is thinner than the overlying Upper Floridan aquifer, and consists of only strata of the middle Eocene Avon Park Formation. Transmissivities in the Lower Floridan aquifer are 8,300 feet squared per day at Richmond Hill and 6,000 feet squared per day at Shellman Bluff, generally one tenth the transmissivity of the Upper Floridan aquifer at these sites. At the southern sites, the upper permeable zone of the Lower Floridan aquifer is thicker than the Upper Floridan aquifer and consists of porous limestone and dolomite interbedded with nonporous strata of the middle Eocene Avon Park and early Eocene Oldsmar Formations. Transmissivities for the upper permeable zone of the Lower Floridan aquifer are 500 feet squared per day at the St Simons Island site and 13,000 feet squared per day at the St Marys site. The Lower Floridan aquifer at the Brunswick and St Marys sites includes the Fernandina permeable zone, which consists of saltwater-bearing dolomite. Hydrographs of Coastal Sound Science Initiative wells and other nearby wells open to the Upper Floridan aquifer, and the upper permeable and Fernandina permeable zones of the Lower Floridan aquifer have similar trends. Water levels in wells open to the Upper and Lower Floridan aquifers are below land surface at the northern sites and the St Simons Island site, and above land surface at the Brunswick and St Marys sites, as of January 1, 2004. Freshwater is present in the Lower Floridan aquifer at Pineora, Pembroke, and St Marys, and from 1,259 to 1,648 feet below land surface at Brunswick. Slightly saline water is present in the Lower Floridan aquifer at Richmond Hill, Shellman Bluff, St Simons Island, and from 1,679 to 1,970 feet below land surface in well 34H495 at Brunswick. The upper permeable zone of the Lower Floridan aquifer contains bicarbonate water at the Pembroke site, sulfate-bicarbonate water at the Brunswick site, and sulfate water at the St Simons Island, Shellman Bluff, St Marys, and Richmond Hill sites. The bicarbonate, sulfate-bicarbonate, and sulfate waters are saturated relative to calcite and dolomite, and undersaturated with gypsum and anhydrite. The Fernandina permeable zone in well 34H495 includes moderately saline water, very saline water, and brine. The Fernandina permeable zone of the Lower Floridan aquifer beneath downtown Brunswick contains chloride water that is slightly undersaturated to saturated with gypsum and anhydrite. Concentrations of total dissolved solids, sulfate, and chloride exceeded the Federal secondary drinking-water standards. The chloride-contaminated plumes beneath downtown Brunswick would require at least a 12- to 20-percent contribution of very saline water from the Fernandi

Georgia↗

USGS2004

Hydrologic and geochemical evaluation of aquifer storage recovery in the Santee Limestone/Black Mingo Aquifer, Charleston, South Carolina, 1998-2002

The hydrologic and geochemical effects of aquifer storage recovery were evaluated to determine the potential for supplying the city of Charleston, South Carolina, with large quantities of potable water during emergencies, such as earthquakes, hurricanes, or hard freezes. An aquifer storage recovery system, including a production well and three observation wells, was installed at a site located on the Charleston peninsula. The focus of this study was the 23.2-meter thick Tertiary-age carbonate and sand aquifer of the Santee Limestone and the Black Mingo Group, the northernmost equivalent of the Floridan aquifer system. Four cycles of injection, storage, and recovery were conducted between October 1999 and February 2002. Each cycle consisted of injecting between 6.90 and 7.19 million liters of water for storage periods of 1, 3, or 6 months. The volume of recovered water that did not exceed the U.S. Environmental Protection Agency secondary standard for chloride (250 milligrams per liter) varied from 1.48 to 2.46 million liters, which is equivalent to 21 and 34 percent of the total volume injected for the individual tests. Aquifer storage recovery testing occurred within two productive zones of the brackish Santee Limestone/Black Mingo aquifer. The individual productive zones were determined to be approximately 2 to 4 meters thick, based on borehole geophysical logs, electromagnetic flow-meter testing, and specific-conductance profiles collected within the observation wells. A transmissivity and storage coefficient of 37 meters squared per day and 3 x 10-5, respectively, were determined for the Santee Limestone/Black Mingo aquifer. Water-quality and sediment samples collected during this investigation documented baseline aquifer and injected water quality, aquifer matrix composition, and changes in injected/aquifer water quality during injection, storage, and recovery. A total of 193 water-quality samples were collected and analyzed for physical properties, major and minor ions, and nutrients. The aquifer and treated surface water were sodiumchloride and calcium/sodium-bicarbonate water types, respectively. Forty-five samples were collected and analyzed for total trihalomethane. Total trihalomethane data collected during aquifer storage recovery cycle 4 indicated that this constituent would not restrict the use of recovered water for drinking-water purposes. Analysis of six sediment samples collected from a cored well located near the aquifer storage recovery site showed that quartz and calcite were the dominant minerals in the Santee Limestone/Black Mingo aquifer. Estimated cation exchange capacity ranged from 12 to 36 milliequivalents per 100 grams in the lower section of the aquifer. A reactive transport model was developed that included two 2-meter thick layers to describe each of the production zones. The four layers composing the production zones were assigned porosities ranging from 0.1 to 0.3 and hydraulic conductivities ranging from 1 to 8.4 meters per day. Specific storage of the aquifer and confining units was estimated to be 1.5 x 10-5 meter-1. Longitudinal dispersivity of all layers was specified to be 0.5 meter. Leakage through the confining unit was estimated to be minimal and, therefore, not used in the reactive transport modeling. Inverse geochemical modeling indicates that mixing, cation exchange, and calcite dissolution are the dominant reactions that occur during aquifer storage recovery testing in the Santee Limestone/Black Mingo aquifer. Potable water injected into the Santee Limestone/Black Mingo aquifer evolved chemically by mixing with brackish background water and reaction with calcite and cation exchangers in the sediment. Reactive-transport model simulations indicated that the calcite and exchange reactions could be treated as equilibrium processes.

South Carolina↗

USGS2002

Field tests of diffusion samplers for inorganic constituents in wells and at a ground-water discharge zone

Field tests were performed on two types of diffusion samplers to collect representative samples of inorganic constituents from ground water in wells and at an arsenic-contaminated ground-water-discharge zone beneath a stream. Nylon-screen samplers and dialysis samplers were tested for the collection of arsenic, calcium, chloride, iron, manganese, sulfate, and dissolved oxygen. The investigations were conducted at the Naval Industrial Reserve Ordnance Plant (NIROP), Fridley, Minnesota, and at the Naval Air Station Fort Worth Joint Reserve Base (NAS Fort Worth JRB), Texas. Data indicate that, in general, nylon-screen and dialysis diffusion samplers are capable of obtaining concentrations of inorganic solutes in ground water that correspond to concentrations obtained by low-flow sampling. Diffusion samplers offer a potentially time-saving approach to well sampling. Particular care must be taken, however, when sampling for iron and other metals, because of the potential for iron precipitation by oxygenation and when dealing with chemically stratified sampling intervals. Simple nylon-screen jar samplers buried beneath creekbed sediment appear to be effective tools for locating discharge zones of arsenic contaminated ground water. Although the LDPE samplers have proven to be inexpensive and simple to use in wells, they are limited by their inability to provide a representative sample of ionic solutes. The success of nylon-screen samplers in sediment studies suggests that these simple samplers may be useful for collecting water samples for inorganic constituents in wells. Results using dialysis bags deployed in wells suggest that these types of samplers have the potential to provide a representative sample of both VOCs and ionic solutes from ground water (Kaplan and others, 1991; Theodore A. Ehlke, U.S. Geological Survey, written commun., 2001). The purpose of this report is to provide results of field tests investigating the potential to use diffusion samplers to collect representative samples of inorganic constituents from ground water in wells and at an arsenic-contaminated ground-water-discharge zone beneath a stream. The investigations were performed at NIROP, Fridley, Minn. (fig. 1) and at NAS Fort Worth JRB, Texas (fig. 2). Two types of samplers were tested. One type was a nylon-screen sampler, which consisted of a 30-mL jar filled with deionized water, with its opening covered by a nylon screen. The second type was a dialysis sampler that consisted of a tube of dialysis membrane filled with deionized water. The nylon-screen samplers were deployed in wells at NIROP Fridley and NAS Fort Worth JRB and beneath the ground-water/surface water interface of a stream at NAS Fort Worth JRB. The dialysis samplers were deployed only in wells at NAS Fort Worth JRB.

Water-Resources Investigations Report↗

USGS2001

Evaluation of passive diffusion bag samplers in selected wells at the Naval Surface Warfare Center, Louisville, Kentucky, July 1999 to January 2000

Passive diffusion bag samplers were tested in 11 wells at the Naval Surface Warfare Center, Louisville, Kentucky, by comparing the volatile organic compound concentrations obtained from passive diffusion bag samplers to volatile organic compound concentrations obtained by pumping the wells. The wells were screened in poorly permeable formations, including overburden, shale, and limestone. In five of the tested wells containing detectable volatile organic compound contamination, the data suggest that the diffusion samplers accurately reflected ambient contaminant concentrations (wells 1-NEC-15-P, 1-NEC-MW17-S, 1-NEMW23-S, 1-NW-MW24-S, and 1-NW-MW24-P). Comparison of a third well (1-NEC-MW34-S), in which the passive diffusion bag samplers produced higher concentrations than the pumped sample, is less certain because the passive diffusion bag sampler had passed through a layer of light non-aqueous phase liquid during deployment, suggesting the possibility of carryover contamination. In two wells (1-NE-MW23-P and 1-NEC-MW15-S), it was unclear whether concentrations obtained by using the passive diffusion bag samplers adequately represented in situ concentrations because the comparison of concentrations obtained by using the samplers and the pump was inconsistent between sampling events and/or between volatile organic compounds. In one well (1-NEC-MW34-P), the methodologies matched poorly, with volatile organic compound concentrations obtained by using the passive diffusion bag sampler substantially lower than those obtained by using the pump. Two of the tested wells (1-NW-MW6-I and 1-SE-MW13-I) contained no detectable contaminants in water obtained from either method. Data from wells where multiple passive diffusion bag samplers were deployed showed the lowest volatile organic compound concentrations adjacent to the vuggy limestone and higher volatile organic compound concentrations deeper in the limestone, supporting colloidal-borescope data that indicate the vuggy limestone is not a zone that supplies water to the wells.

Kentucky↗

USGS2001

Biodegradation potential of chlorinated solvents in ground water at the Naval Surface Warfare Center, Louisville, Kentucky, July 1999 to February 2000

The U.S. Geological Survey, in cooperation with the U.S. Department of the Navy, Southern Division Naval Facilities Engineering Command, investigated the potential for biodegradation of chlorinated solvents in ground water at the Naval Surface Warfare Center (also known as the Naval Ordnance Station, or the station), Louisville, Kentucky. The subsurface down to at least 100 feet at the station is characterized, from shallowest to deepest, by overburden deposits, a shale layer, and limestone. In general, all of the strata are poorly permeable. The permeable zones of the overburden and the limestone make up the overburden aquifer and the bedrock aquifer, respectively. Observed concentrations of redox-sensitive solutes suggest that the predominant anaerobic terminal electron accepting process in the overburden aquifer can shift between iron reduction and sulfate reduction, possibly as a result of rainfall-induced oxidation events. Daughter-product concentrations and laboratory experiments indicate that a variety of mechanisms, including reductive dechlorination and cometabolic oxidation, appear to be actively

Kentucky↗

USGS2000

Field testing of passive diffusion bag samplers for volatile organic compound concentrations in ground water, Naval Industrial Reserve Ordnance Plant, Fridley, Minnesota, November 1999 and May 2000

Volatile organic compound concentrations from passive diffusion bag samplers were compared with concentrations from conventional purge (three or more casing volumes) sampling and low-flow purge sampling in side-by-side tests in 17 wells at the Naval Industrial Reserve Ordnance Plant, in Fridley, Minnesota. An initial comparison of 1,2-dichloroethene and trichloroethene concentrations obtained by using passive diffusion bag samplers and the conventional purge method in wells where one passive diffusion bag sampler was deployed showed good agreement at several wells but poor agreement at others. Collection of data from multiple diffusion samplers during the conventional purge sampling and during the low-flow sampling, however, suggests that the volatile organic compound concentrations from the passive diffusion bag samplers accurately reflect the volatile organic compound distribution in the screened interval, whereas the conventional purge and low-flow purge samples reflect mixing during pumping. The data also show that contaminant stratification was present in some wells. In one well, trichloroethene concentrations ranged from 470 to 1,600 micrograms per liter over a vertical distance of approximately 6 feet.

Water-Resources Investigations Report↗