Arsenic, microbes and contaminated aquifers

Science.gov (United States)

Oremland, Ronald S.; Stolz, John F.

2005-01-01

The health of tens of millions of people world-wide is at risk from drinking arsenic-contaminated well water. In most cases this arsenic occurs naturally within the sub-surface aquifers, rather than being derived from identifiable point sources of pollution. The mobilization of arsenic into the aqueous phase is the first crucial step in a process that eventually leads to human arsenicosis. Increasing evidence suggests that this is a microbiological phenomenon.

Intrinsic bioremediation of petroleum hydrocarbons in a gas condensate-contaminated aquifer

International Nuclear Information System (INIS)

Gieg, L.M.; McInerney; Tanner, R.S.; Harris, S.H. Jr.; Sublette, K.L.; Suflita, J.M.; Kolhatkar, R.V.

1999-01-01

A study was designed to determine if the intrinsic bioremediation of gas condensate hydrocarbons represented an important fate process in a shallow aquifer underlying a natural gas production site. For over 4 yr, changes in the groundwater, sediment, and vadose zone chemistry in the contaminated portion of the aquifer were interpreted relative to a background zone. Changes included decreased dissolved oxygen and sulfate levels and increased alkalinity, Fe(II), and methane concentrations in the contaminated groundwater, suggesting that aerobic heterotrophic respiration depleted oxygen reserves leaving anaerobic conditions in the hydrocarbon-impacted subsurface. Dissolved hydrogen levels in the contaminated groundwater indicated that sulfate reduction and methanogenesis were predominant biological processes, corroborating the geochemical findings. Furthermore, 10--1000-fold higher numbers of sulfate reducers and methanogens were enumerated in the contaminated sediment relative to background. Putative metabolites were also detected in the contaminated groundwater, including methylbenzylsuccinic acid, a signature intermediate of anaerobic xylene decay. Laboratory incubations showed that benzene, toluene, ethylbenzene, and each of the xylene isomers were biodegraded under sulfate-reducing conditions as was toluene under methanogenic conditions. These results coupled with a decrease in hydrocarbon concentrations in contaminated sediment confirm that intrinsic bioremediation contributes to the attenuation of hydrocarbons in this aquifer

Semianalytical solutions for contaminant transport under variable velocity field in a coastal aquifer

Science.gov (United States)

Koohbor, Behshad; Fahs, Marwan; Ataie-Ashtiani, Behzad; Simmons, Craig T.; Younes, Anis

2018-05-01

Existing closed-form solutions of contaminant transport problems are limited by the mathematically convenient assumption of uniform flow. These solutions cannot be used to investigate contaminant transport in coastal aquifers where seawater intrusion induces a variable velocity field. An adaptation of the Fourier-Galerkin method is introduced to obtain semi-analytical solutions for contaminant transport in a confined coastal aquifer in which the saltwater wedge is in equilibrium with a freshwater discharge flow. Two scenarios dealing with contaminant leakage from the aquifer top surface and contaminant migration from a source at the landward boundary are considered. Robust implementation of the Fourier-Galerkin method is developed to efficiently solve the coupled flow, salt and contaminant transport equations. Various illustrative examples are generated and the semi-analytical solutions are compared against an in-house numerical code. The Fourier series are used to evaluate relevant metrics characterizing contaminant transport such as the discharge flux to the sea, amount of contaminant persisting in the groundwater and solute flux from the source. These metrics represent quantitative data for numerical code validation and are relevant to understand the effect of seawater intrusion on contaminant transport. It is observed that, for the surface contamination scenario, seawater intrusion limits the spread of the contaminant but intensifies the contaminant discharge to the sea. For the landward contamination scenario, moderate seawater intrusion affects only the spatial distribution of the contaminant plume while extreme seawater intrusion can increase the contaminant discharge to the sea. The developed semi-analytical solution presents an efficient tool for the verification of numerical models. It provides a clear interpretation of the contaminant transport processes in coastal aquifers subject to seawater intrusion. For practical usage in further studies, the full

Protists from a sewage‐contaminated aquifer on cape cod, Massachusetts

Science.gov (United States)

Novarino, Gianfranco; Warren, Alan; Kinner, Nancy E.; Harvey, Ronald W.

1994-01-01

Several species of flagellates (genera Bodo, Cercomonas, Cryptaulax, Cyathomonas, Goniomonas, Spumella) have been identified in cultures from a plume of organic contamination (treated sewage effluent) within an aquifer on Cape Cod, Massachusetts. Amoebae and numerous unidentifiable 2‐ to 3‐μm flagellates have also been observed. As a rule, flagellates were associated with solid surfaces, or were capable of temporary surface attachment, corroborating earlier observations from in situ and column transport experiments suggesting that protists in the Massachusetts aquifer have a high propensity for association with sediment grain surfaces. Based on the fact that cultures from the uncontaminated part of the aquifer yielded only a few species of protists, it is hypothesized that the greater abundance and variety of food sources in the contaminant plume is capable of supporting a greater number of protistan species.

The supposed radioactive contamination of the Puelche aquifer

International Nuclear Information System (INIS)

Martini, Leopoldo E.

2005-01-01

The paper attempts to clarify the supposed radioactive contamination of the Puelche Aquifer in the Ezeiza Atomic Center Area, Ezeiza, province of Buenos Aires (Argentina). Reports are listed that show categorically that no anthropogenic uranium contamination is present. As far as the nitrates contamination is concerned, it is not generated by the Ezeiza Atomic Center, because the Center is downward from the contaminated zone. It is possible that the contamination is produced by houses in the area without suitable sewage. In the present case the best contribution to the environmental right, besides the adaptation and the systematization of the different legal instruments, is to found the analysis of the facts on the scientific and technical knowledge. (author) [es

Sustainable Technologies and Social Costs for Eliminating Contamination of an Aquifer

Directory of Open Access Journals (Sweden)

Mario Schirmer

2010-07-01

Full Text Available This case study deals with long-term contamination of the Leuna aquifer, which is intended to be restored using sustainable technologies financed by the state. The contamination can only be solved using active rather than passive intervention, because the aquifer has an extraordinarily low natural attenuation capacity for the specific pollutants. Due to the longevity of the contamination source, the groundwater treatment technology that was chosen for the site must operate for a minimum of 20 years but probably much longer. Since the polluter-pay principle cannot be applied, the estimated dynamic primary remediation costs must be accepted as a political or social cost, which must be paid by current and future generations.

Assessing the vulnerability of public-supply wells to contamination--Glacial aquifer system in Woodbury, Connecticut

Science.gov (United States)

Jagucki, Martha L.; Brown, Craig J.; Starn, J. Jeffrey; Eberts, Sandra M.

2010-01-01

, as indicated by the solvents, fuel components, road salt, and septic-system leachate that were detected in the glacial aquifer system during the current study. Age-dating combined with chemical modeling suggests that less than 2 percent of water produced by the public-supply well is water from the deep bedrock that is "old" (water that recharged, or entered, the aquifer before 1952). Such a small percentage of old groundwater entering the public-supply well offers little potential for dilution of young waters containing contaminants from human activities. Shallow groundwater that originated as recharge through urban areas generally had higher median concentrations and more detections of volatile organic compounds (VOCs) than did groundwater from the deep glacial deposits or fractured bedrock that originated mainly as recharge through agricultural and undeveloped land. Shallow groundwater was also found to be affected by road salt and septic-system leachate. A chemical mixing model indicates that up to 15 percent of nitrate in water from the supply well is likely from septic-system leachate. The Connecticut Department of Public Health has identified several potential sources of contamination in the commercial area of Woodbury (several light industrial or commercial properties where hazardous materials and petroleum products are used and stored). To reduce stormwater runoff in the commercial area, water from the parking lots and pavement is channeled into dry wells-drains that shunt water directly into the aquifer system, bypassing the soil and unsaturated zones. A computer-model simulation of groundwater flow indicates that approximately 16 percent of the water produced by the public-supply well is derived from runoff captured by these drains. Traveltime for water from the dry wells to the public-supply well ranges from about 1.5 to less than 4 years. Dry wells have the potential to enhance contaminant movement to the supply well, suggesting that stormwater

Applicability of slug interference testing of hydraulic characterization of contaminated aquifer sites

International Nuclear Information System (INIS)

Spane, F.A.; Swanson, L.C.

1993-10-01

Aquifer test methods available for characterizing hazardous waste sites are sometimes restricted because of problems with disposal of contaminated groundwater. These problems, in part, have made slug tests a more desirable method of determining hydraulic properties at such sites. However, in higher permeability formations (i.e., transmissivities ≥ 1 x 10 -3 m 2 /s), slug test results often cannot be analyzed and give, at best, only a lower limit for transmissivity. A need clearly exists to develop test methods that can be used to characterize higher permeability aquifers without removing large amounts of contaminated groundwater. One hydrologic test method that appears to hold promise for characterizing such sites is the slug interference test. To assess the applicability of this test method for use in shallow alluvial aquifer systems, slug interference tests have been conducted, along with more traditional aquifer testing methods, at several Hanford multiple-well sites. Transmissivity values estimated from the slug interference tests were comparable (within a factor of 2 to 3) to values calculated using traditional testing methods, and made it possible to calculate the storativity or specific yield for the intervening test formation. The corroboration of test results indicates that slug interference testing is a viable hydraulic characterization method in transmissive alluvial aquifers, and may represent one of the few test methods that can be used in sensitive areas where groundwater is contaminated

Adaptations of indigenous bacteria to fuel contamination in karst aquifers in south-central Kentucky

Science.gov (United States)

Byl, Thomas D.; Metge, David W.; Agymang, Daniel T.; Bradley, Michael W.; Hileman, Gregg; Harvey, Ronald W.

2014-01-01

The karst aquifer systems in southern Kentucky can be dynamic and quick to change. Microorganisms that live in these unpredictable aquifers are constantly faced with environmental changes. Their survival depends upon adaptations to changes in water chemistry, taking advantage of positive stimuli and avoiding negative environmental conditions. The U.S. Geological Survey conducted a study in 2001 to determine the capability of bacteria to adapt in two distinct regions of water quality in a karst aquifer, an area of clean, oxygenated groundwater and an area where the groundwater was oxygen depleted and contaminated by jet fuel. Water samples containing bacteria were collected from one clean well and two jet fuel contaminated wells in a conduit-dominated karst aquifer. Bacterial concentrations, enumerated through direct count, ranged from 500,000 to 2.7 million bacteria per mL in the clean portion of the aquifer, and 200,000 to 3.2 million bacteria per mL in the contaminated portion of the aquifer over a twelve month period. Bacteria from the clean well ranged in size from 0.2 to 2.5 mm, whereas bacteria from one fuel-contaminated well were generally larger, ranging in size from 0.2 to 3.9 mm. Also, bacteria collected from the clean well had a higher density and, consequently, were more inclined to sink than bacteria collected from contaminated wells. Bacteria collected from the clean portion of the karst aquifer were predominantly (,95%) Gram-negative and more likely to have flagella present than bacteria collected from the contaminated wells, which included a substantial fraction (,30%) of Gram-positive varieties. The ability of the bacteria from the clean portion of the karst aquifer to biodegrade benzene and toluene was studied under aerobic and anaerobic conditions in laboratory microcosms. The rate of fuel biodegradation in laboratory studies was approximately 50 times faster under aerobic conditions as compared to anaerobic, sulfur-reducing conditions. The

Effects of Subsurface Microbial Ecology on Geochemical Evolution of a Crude-Oil Contaminated Aquifer

Science.gov (United States)

Bekins, B. A.; Cozzarelli, I. M.; Godsy, E. M.; Warren, E.; Hostettler, F. D.

2001-12-01

We have identified several subsurface habitats for microorganisms in a crude oil contaminated located near Bemidji, Minnesota. These aquifer habitats include: 1) the unsaturated zone contaminated by hydrocarbon vapors, 2) the zones containing separate-phase crude oil, and 3) the aqueous-phase contaminant plume. The surficial glacial outwash aquifer was contaminated when a crude oil pipeline burst in 1979. We analyzed sediment samples from the contaminated aquifer for the most probable numbers of aerobes, iron reducers, fermenters, and three types of methanogens. The microbial data were then related to gas, water, and oil chemistry, sediment extractable iron, and permeability. The microbial populations in the various contaminated subsurface habitats each have special characteristics and these affect the aquifer and contaminant chemistry. In the eight-meter-thick, vapor-contaminated vadose zone, a substantial aerobic population has developed that is supported by hydrocarbon vapors and methane. Microbial numbers peak in locations where access to both hydrocarbons and nutrients infiltrating from the surface is maximized. The activity of this population prevents hydrocarbon vapors from reaching the land surface. In the zone where separate-phase crude oil is present, a consortium of methanogens and fermenters dominates the populations both above and below the water table. Moreover, gas concentration data indicate that methane production has been active in the oily zone since at least 1986. Analyses of the extracted separate-phase oil show that substantial degradation of C15 -C35 n-alkanes has occurred since 1983, raising the possibility that significant degradation of C15 and higher n-alkanes has occurred under methanogenic conditions. However, lab and field data suggest that toxic inhibition by crude oil results in fewer acetate-utilizing methanogens within and adjacent to the separate-phase oil. Data from this and other sites indicate that toxic inhibition of

Factors affecting the distribution of hydrocarbon contaminants and hydrogeochemical parameters in a shallow sand aquifer

Science.gov (United States)

Lee, Jin-Yong; Cheon, Jeong-Yong; Lee, Kang-Kun; Lee, Seok-Young; Lee, Min-Hyo

2001-07-01

The distributions of hydrocarbon contaminants and hydrogeochemical parameters were investigated in a shallow sand aquifer highly contaminated with petroleum hydrocarbons leaked from solvent storage tanks. For these purposes, a variety of field investigations and studies were performed, which included installation of over 100 groundwater monitoring wells and piezometers at various depths, soil logging and analyses during well and piezometer installation, chemical analysis of groundwater, pump tests, and slug tests. Continuous water level monitoring at three selected wells using automatic data-logger and manual measuring at other wells were also conducted. Based on analyses of the various investigations and tests, a number of factors were identified to explain the distribution of the hydrocarbon contaminants and hydrogeochemical parameters. These factors include indigenous biodegradation, hydrostratigraphy, preliminary pump-and-treat remedy, recharge by rainfall, and subsequent water level fluctuation. The permeable sandy layer, in which the mean water table elevation is maintained, provided a dominant pathway for contaminant transport. The preliminary pump-and-treat action accelerated the movement of the hydrocarbon contaminants and affected the redox evolution pattern. Seasonal recharge by rain, together with indigenous biodegradation, played an important role in the natural attenuation of the petroleum hydrocarbons via mixing/dilution and biodegradation. The water level fluctuations redistributed the hydrocarbon contaminants by partitioning them into the soil and groundwater. The identified factors are not independent but closely inter-correlated.

Modeling contaminant plumes in fractured limestone aquifers

DEFF Research Database (Denmark)

Mosthaf, Klaus; Brauns, Bentje; Fjordbøge, Annika Sidelmann

Determining the fate and transport of contaminant plumes from contaminated sites in limestone aquifers is important because they are a major drinking water resource. This is challenging because they are often heavily fractured and contain chert layers and nodules, resulting in a complex transport...... model. The paper concludes with recommendations on how to identify and employ suitable models to advance the conceptual understanding and as decision support tools for risk assessment and the planning of remedial actions....... behavior. Improved conceptual models are needed for this type of site. Here conceptual models are developed by combining numerical models with field data. Several types of fracture flow and transport models are available for the modeling of contaminant transport in fractured media. These include...... the established approaches of the equivalent porous medium, discrete fracture and dual continuum models. However, these modeling concepts are not well tested for contaminant plume migration in limestone geologies. Our goal was to develop and evaluate approaches for modeling the transport of dissolved contaminant...

Effect of Short-Circuit Pathways on Water Quality in Selected Confined Aquifers (Invited)

Science.gov (United States)

McMahon, P. B.

2010-12-01

Confined aquifers in the United States generally contain fewer anthropogenic contaminants than unconfined aquifers because confined aquifers often contain water recharged prior to substantial human development and redox conditions are more reducing, which favors degradation of common contaminants like nitrate and chlorinated solvents. Groundwater in a confined part of the High Plains aquifer near York, Nebraska had an adjusted radiocarbon age of about 2,000 years, and groundwater in a confined part of the Floridan aquifer near Tampa, Florida had apparent ages greater than 60 years on the basis of tritium measurements. Yet compounds introduced more recently into the environment (anthropogenic nitrate and volatile organic compounds) were detected in selected public-supply wells completed in both aquifers. Depth-dependent measurements of flow and chemistry in the pumping supply wells, groundwater age dating, numerical modeling of groundwater flow, and other monitoring data indicated that the confined aquifers sampled by the supply wells were connected to contaminated unconfined aquifers by short-circuit pathways. In the High Plains aquifer, the primary pathways appeared to be inactive irrigation wells screened in both the unconfined and confined aquifers. In the Floridan aquifer, the primary pathways were karst sinkholes and conduits. Heavy pumping in both confined systems exacerbated the problem by reducing the potentiometric surface and increasing groundwater velocities, thus enhancing downward gradients and reducing reaction times for processes like denitrification. From a broader perspective, several confined aquifers in the U.S. have experienced large declines in their potentiometric surfaces because of groundwater pumping and this could increase the potential for contamination in those aquifers, particularly where short-circuit pathways connect them to shallower, contaminated sources of water, such as was observed in York and Tampa.

Global aquifers dominated by fossil groundwaters but wells vulnerable to modern contamination

Science.gov (United States)

Jasechko, Scott; Perrone, Debra; Befus, Kevin M.; Bayani Cardenas, M.; Ferguson, Grant; Gleeson, Tom; Luijendijk, Elco; McDonnell, Jeffrey J.; Taylor, Richard G.; Wada, Yoshihide; Kirchner, James W.

2017-06-01

The vulnerability of groundwater to contamination is closely related to its age. Groundwaters that infiltrated prior to the Holocene have been documented in many aquifers and are widely assumed to be unaffected by modern contamination. However, the global prevalence of these `fossil' groundwaters and their vulnerability to modern-era pollutants remain unclear. Here we analyse groundwater carbon isotope data (12C, 13C, 14C) from 6,455 wells around the globe. We show that fossil groundwaters comprise a large share (42-85%) of total aquifer storage in the upper 1 km of the crust, and the majority of waters pumped from wells deeper than 250 m. However, half of the wells in our study that are dominated by fossil groundwater also contain detectable levels of tritium, indicating the presence of much younger, decadal-age waters and suggesting that contemporary contaminants may be able to reach deep wells that tap fossil aquifers. We conclude that water quality risk should be considered along with sustainable use when managing fossil groundwater resources.

Removal of petroleum-derived hydrocarbons from contaminated soils by solvent extraction

International Nuclear Information System (INIS)

Ladanowski, C.; Petti, L.

1993-01-01

Laboratory studies were conducted using hexane for the removal of light crude oil from contaminated sand, peat, and clay soils. The bench-scale process tested consists of three major steps: solvent washing, settling/decantation/filtration of extract, and solvent recycle. The results indicate that the use of solvent extraction for cleanup of oil-contaminated soils is an effective technology at the bench-scale level. Using a 1,000 g batch system, extremely high oil removal efficiencies were obtained from contaminated sand (up to 98.9%) and peat soil (up to 83.9%). The final oil contaminant concentration for sand varied between 0.06% and 0.39%, while that for peat soil varied between 1.52% and 5.21%. The guidelines for the decommissioning and cleanup of sites in Ontario for oil and grease (1 wt %) were met in all instances for the treated sand. Hexane recovery from diesel-contaminated sand and peat soil experiments was ca 81% and 67% respectively. 4 refs., 6 figs., 10 tabs

New methodology to investigate potential contaminant mass fluxes at the stream-aquifer interface by combining integral pumping tests and streambed temperatures

International Nuclear Information System (INIS)

Kalbus, E.; Schmidt, C.; Bayer-Raich, M.; Leschik, S.; Reinstorf, F.; Balcke, G.U.; Schirmer, M.

2007-01-01

The spatial pattern and magnitude of mass fluxes at the stream-aquifer interface have important implications for the fate and transport of contaminants in river basins. Integral pumping tests were performed to quantify average concentrations of chlorinated benzenes in an unconfined aquifer partially penetrated by a stream. Four pumping wells were operated simultaneously for a time period of 5 days and sampled for contaminant concentrations. Streambed temperatures were mapped at multiple depths along a 60 m long stream reach to identify the spatial patterns of groundwater discharge and to quantify water fluxes at the stream-aquifer interface. The combined interpretation of the results showed average potential contaminant mass fluxes from the aquifer to the stream of 272 μg m -2 d -1 MCB and 71 μg m -2 d -1 DCB, respectively. This methodology combines a large-scale assessment of aquifer contamination with a high-resolution survey of groundwater discharge zones to estimate contaminant mass fluxes between aquifer and stream. - We provide a new methodology to quantify the potential contaminant mass flux from an aquifer to a stream

Quality of Nevada's aquifers and their susceptibility to contamination, 1990-2004

Science.gov (United States)

Lopes, Thomas J.

2006-01-01

EXECUTIVE SUMMARY: In 1999, the U.S. Environmental Protection Agency introduced a rule to protect the quality of ground water in areas other than source-water protection areas. These other sensitive ground-water areas (OSGWA) are areas that are not currently but could eventually be used as a source of drinking water. To help determine whether a well is in an OSGWA, the Nevada Division of Environmental Protection needs statewide information on the susceptibility and vulnerability of Nevada's aquifer systems to contamination. This report presents an evaluation of the quality of ground water and susceptibility of Nevada's aquifer systems to anthropogenic contamination. Chemical tracers and statistical methods were used to assess the susceptibility of aquifer systems in Nevada. Chemical tracers included nitrate, pesticides, volatile organic compounds (VOCs), chlorofluorocarbons (CFCs), dissolved gases, and isotopes of hydrogen and oxygen. Ground-water samples were collected from 133 wells during August 2002 through October 2003. Logistic regression was done to estimate the probability of detecting nitrate above concentrations typically found in undeveloped areas. Nitrate is one of the most common anthropogenic contaminants that degrades ground-water quality, is commonly measured and is persistent, except in reducing conditions. These characteristics make nitrate a good indicator of aquifer susceptibility. Water-quality data for 5,528 wells were compiled into a database. The area around each well was characterized using information on explanatory variables that could be related to nitrate concentrations. Data also were used to characterize the quality of ground water in Nevada, including dissolved solids, nitrate, pesticide, and VOC concentrations.

Determination of timescales of nitrate contamination by groundwater age models in a complex aquifer system

Science.gov (United States)

Koh, E. H.; Lee, E.; Kaown, D.; Lee, K. K.; Green, C. T.

2017-12-01

Timing and magnitudes of nitrate contamination are determined by various factors like contaminant loading, recharge characteristics and geologic system. Information of an elapsed time since recharged water traveling to a certain outlet location, which is defined as groundwater age, can provide indirect interpretation related to the hydrologic characteristics of the aquifer system. There are three major methods (apparent ages, lumped parameter model, and numerical model) to date groundwater ages, which differently characterize groundwater mixing resulted by various groundwater flow pathways in a heterogeneous aquifer system. Therefore, in this study, we compared the three age models in a complex aquifer system by using observed age tracer data and reconstructed history of nitrate contamination by long-term source loading. The 3H-3He and CFC-12 apparent ages, which did not consider the groundwater mixing, estimated the most delayed response time and a highest period of the nitrate loading had not reached yet. However, the lumped parameter model could generate more recent loading response than the apparent ages and the peak loading period influenced the water quality. The numerical model could delineate various groundwater mixing components and its different impacts on nitrate dynamics in the complex aquifer system. The different age estimation methods lead to variations in the estimated contaminant loading history, in which the discrepancy in the age estimation was dominantly observed in the complex aquifer system.

Delineation of the extent of milling-related contamination in a naturally contaminated aquifer system

International Nuclear Information System (INIS)

Downs, William F.; Storms, Erik F.

1992-01-01

Uranium mill tailings from the Susquehanna-Western mill near Falls City, Texas, were pumped to tailings ponds located in abandoned open pit uranium mines. The ores from these mines were oxidized. Uranium and the associated hazardous constituents were present in these ores as relatively soluble secondary minerals. Because the tailings piles are located on the outcrops of the units designated as the uppermost aquifer, there is no upgradient aquifer from which to establish 'background' water quality. The widespread mineralization in the area naturally imposes a large variability in water quality in these units. It was necessary to demonstrate to State and Federal regulators that selected downgradient wells were beyond the influence of milling operations, and to develop a series of 'indicator parameters' that could be used to differentiate milling contaminated groundwater from that native to the aquifer. (author)

Phylogenetic and functional diversity within toluene-degrading, sulphate-reducing consortia enriched from a contaminated aquifer.

Science.gov (United States)

Kuppardt, Anke; Kleinsteuber, Sabine; Vogt, Carsten; Lüders, Tillmann; Harms, Hauke; Chatzinotas, Antonis

2014-08-01

Three toluene-degrading microbial consortia were enriched under sulphate-reducing conditions from different zones of a benzene, toluene, ethylbenzene and xylenes (BTEX) plume of two connected contaminated aquifers. Two cultures were obtained from a weakly contaminated zone of the lower aquifer, while one culture originated from the highly contaminated upper aquifer. We hypothesised that the different habitat characteristics are reflected by distinct degrader populations. Degradation of toluene with concomitant production of sulphide was demonstrated in laboratory microcosms and the enrichment cultures were phylogenetically characterised. The benzylsuccinate synthase alpha-subunit (bssA) marker gene, encoding the enzyme initiating anaerobic toluene degradation, was targeted to characterise the catabolic diversity within the enrichment cultures. It was shown that the hydrogeochemical parameters in the different zones of the plume determined the microbial composition of the enrichment cultures. Both enrichment cultures from the weakly contaminated zone were of a very similar composition, dominated by Deltaproteobacteria with the Desulfobulbaceae (a Desulfopila-related phylotype) as key players. Two different bssA sequence types were found, which were both affiliated to genes from sulphate-reducing Deltaproteobacteria. In contrast, the enrichment culture from the highly contaminated zone was dominated by Clostridia with a Desulfosporosinus-related phylotype as presumed key player. A distinct bssA sequence type with high similarity to other recently detected sequences from clostridial toluene degraders was dominant in this culture. This work contributes to our understanding of the niche partitioning between degrader populations in distinct compartments of BTEX-contaminated aquifers.

Glacial recharge, salinisation and anthropogenic contamination in the coastal aquifers of Recife (Brazil)

Energy Technology Data Exchange (ETDEWEB)

Chatton, E., E-mail: eliot.chatton@gmail.com [Géosciences Rennes, Université Rennes 1-CNRS, UMR 6118, adress: 263 av du général Leclerc, Campus de Beaulieu, bat 15, 35042 Rennes Cedex (France); Aquilina, L., E-mail: luc.aquilina@univ-rennes1.fr [Géosciences Rennes, Université Rennes 1-CNRS, UMR 6118, adress: 263 av du général Leclerc, Campus de Beaulieu, bat 15, 35042 Rennes Cedex (France); Pételet-Giraud, E., E-mail: e.petelet@brgm.fr [Bureau de Recherches Géologiques et Minières (BRGM), adress: 3 avenue Claude-Guillemin, BP 36009, 45060 Orléans Cedex 2 (France); Cary, L., E-mail: l.cary@brgm.fr [Bureau de Recherches Géologiques et Minières (BRGM), adress: 3 avenue Claude-Guillemin, BP 36009, 45060 Orléans Cedex 2 (France); Bertrand, G., E-mail: guillaume353@gmail.com [Instituto de Geociências, CEPAS (Groundwater Research Center), University of São Paulo, adress: Rua do lago 562, 05508-080 Sao Paulo (Brazil); Labasque, T., E-mail: thierry.labasque@univ-rennes1.fr [Géosciences Rennes, Université Rennes 1-CNRS, UMR 6118, adress: 263 av du général Leclerc, Campus de Beaulieu, bat 15, 35042 Rennes Cedex (France); and others

2016-11-01

Implying large residence times and complex water origins deep coastal aquifers are of particular interest as they are remarkable markers of climate, water use and land use changes. Over the last decades, the Metropolitan Region of Recife (Brazil) went through extensive environmental changes increasing the pressure on water resources and giving rise to numerous environmental consequences on the coastal groundwater systems. We analysed the groundwater of the deep aquifers Cabo and Beberibe that are increasingly exploited. The processes potentially affecting groundwater residence times and flow paths have been studied using a multi-tracer approach (CFCs, SF6, noble gases, 14C, 2H and 18O). The main findings of these investigations show that: (1) Groundwaters of the Cabo and Beberibe aquifers have long residence times and were recharged about 20,000 years ago. (2) Within these old groundwaters we can find palaeo-climate evidences from the last glacial period at the tropics with lower temperatures and dryer conditions than the present climate. (3) Recently, the natural slow dynamic of these groundwater systems was significantly affected by mixing processes with contaminated modern groundwater coming from the shallow unconfined Boa Viagem aquifer. (4) The large exploitation of these aquifers leads to a modification of the flow directions and causes the intrusion through palaeo-channels of saline water probably coming from the Capibaribe River and from the last transgression episodes. These observations indicate that the current exploitation of the Cabo and Beberibe aquifers is unsustainable regarding the long renewal times of these groundwater systems as well as their ongoing contamination and salinisation. The groundwater cycle being much slower than the human development rhythm, it is essential to integrate the magnitude and rapidity of anthropogenic impacts on this extremely slow cycle to the water management concepts. - Highlights: • Study of anthropogenic impacts

Glacial recharge, salinisation and anthropogenic contamination in the coastal aquifers of Recife (Brazil)

International Nuclear Information System (INIS)

Chatton, E.; Aquilina, L.; Pételet-Giraud, E.; Cary, L.; Bertrand, G.; Labasque, T.

2016-01-01

Implying large residence times and complex water origins deep coastal aquifers are of particular interest as they are remarkable markers of climate, water use and land use changes. Over the last decades, the Metropolitan Region of Recife (Brazil) went through extensive environmental changes increasing the pressure on water resources and giving rise to numerous environmental consequences on the coastal groundwater systems. We analysed the groundwater of the deep aquifers Cabo and Beberibe that are increasingly exploited. The processes potentially affecting groundwater residence times and flow paths have been studied using a multi-tracer approach (CFCs, SF6, noble gases, 14C, 2H and 18O). The main findings of these investigations show that: (1) Groundwaters of the Cabo and Beberibe aquifers have long residence times and were recharged about 20,000 years ago. (2) Within these old groundwaters we can find palaeo-climate evidences from the last glacial period at the tropics with lower temperatures and dryer conditions than the present climate. (3) Recently, the natural slow dynamic of these groundwater systems was significantly affected by mixing processes with contaminated modern groundwater coming from the shallow unconfined Boa Viagem aquifer. (4) The large exploitation of these aquifers leads to a modification of the flow directions and causes the intrusion through palaeo-channels of saline water probably coming from the Capibaribe River and from the last transgression episodes. These observations indicate that the current exploitation of the Cabo and Beberibe aquifers is unsustainable regarding the long renewal times of these groundwater systems as well as their ongoing contamination and salinisation. The groundwater cycle being much slower than the human development rhythm, it is essential to integrate the magnitude and rapidity of anthropogenic impacts on this extremely slow cycle to the water management concepts. - Highlights: • Study of anthropogenic impacts

Perched aquifers - their potential impact on contaminant transport in the southern High Plains, Texas

International Nuclear Information System (INIS)

Mullican, W.F. III; Fryar, A.E.; Johns, N.D.

1993-01-01

Understanding the hydrogeology and hydrochemistry of perched aquifers at potential and known contaminated waste sites has become increasingly important because of the impact these aquifers may have on contaminant transport independent of regional aquifer processes. Investigations of a perched aquifer above the Ogallala aquifer are being conducted in the region of the U.S. Department of Energy's Pantex Plant, a proposed Superfund site, located approximately 20 mi northeast of Amarillo, Texas. Since the early 1950s, a small playa basin located on the Pantex Plant has been used as a waste-water discharge pond with daily discharge rates ranging from 400,000 to 1 million gal. The focus of this investigation is an unconfined, perched aquifer that overlies a thick silty clay sequence within the upper, mostly unsaturated part of the Ogallala Formation (Neogene). In the area of the Pantex Plant, measured depths to the perched aquifer range from 200 to 300 ft below land surface, whereas depth to the regional Ogallala aquifer ranges from 375 to 500 ft. The potentiometric surface of the perched aquifer typically represents groundwater mounds proximal to the playas and thins into trough in the interplaya areas. Hydrologic gradients of the primary mound under investigation are relatively high, ranging from 28 to 45 ft/mi. Calculated transmissivities have a geometric mean of 54 ft 2 /day, with saturated thicknesses ranging from 4 to 1000 ft. Modeling of the perched aquifer was designed to determine how much, if any, discharge to the small playa basin has enhanced recharge to the perched aquifers and increased the vertical and lateral extent of the perched aquifer. Preliminary results indicate that measurements of vertical conductance through the perching silty-clay sequence and recharge rates through playas are critical for calibrating the model. Accurate delineation of rates and flow directions in the perched aquifer is critical to any successful remediation effort

Assessing the susceptibility to contamination of two aquifer systems used for public water supply in the Modesto and Fresno metropolitan areas, California, 2001 and 2002

Science.gov (United States)

Wright, Michael T.; Belitz, Kenneth; Johnson, Tyler D.

2004-01-01

Ground-water samples were collected from 90 active public supply wells in the Fresno and Modesto metropolitan areas as part of the California Aquifer Susceptibility (CAS) program. The CAS program was formed to examine the susceptibility to contamination of aquifers that are tapped by public supply wells to serve the citizens of California. The objectives of the program are twofold: (1) to evaluate the quality of ground water used for public supply using volatile organic compound (VOC) concentrations in ground-water samples and (2) to determine if the occurrence and distribution of low level VOCs in ground water and characteristics, such as land use, can be used to predict aquifer susceptibility to contamination from anthropogenic activities occurring at, or near, land surface. An evaluation was made of the relation between VOC occurrence and the explanatory variables: depth to the top of the uppermost well perforation, land use, relative ground-water age, high nitrate concentrations, density of leaking underground fuel tanks (LUFT), and source of recharge water. VOCs were detected in 92 percent of the wells sampled in Modesto and in 72 percent of the wells sampled in Fresno. Trihalomethanes (THM) and solvents were frequently detected in both study areas. Conversely, the gasoline components?benzene, toluene ethylbenzene, and xylenes (BTEX)?were rarely, if at all, detected, even though LUFTs were scattered throughout both study areas. The rare occurrence of BTEX compounds may be the result of their low solubility and labile nature in the subsurface environment. Samples were analyzed for 85 VOCs; 25 were detected in at least one sample. The concentrations of nearly all VOCs detected were at least an order of magnitude below action levels set by drinking water standards. Concentrations of four VOCs exceeded federal and state maximum contaminant levels (MCL): the solvent trichloroethylene (TCE) and the fumigant 1, 2-dibromo-3-chloropropane (DBCP) in Fresno, and the

Radon distribution in a gasoline-contaminated aquifer

International Nuclear Information System (INIS)

Fan, K.; Kuo, T.; Han, Y.; Chen, C.; Lin, C.; Lee, C.

2007-01-01

Naturally occurring radon-222 gas in groundwater was investigated as a partitioning tracer to detect non-aqueous phase liquid (NAPL) in a gasoline-contaminated aquifer. The radon-222 activity of groundwater decreased significantly from an average of 7.38+/-1.68BqL -1 measured in monitoring wells located upgradient in the uncontaminated zone to an average of 2.30+/-0.60BqL -1 measured in monitoring wells inside the NAPL source zone. Meanwhile, the radium-226 concentrations measured in aquifer matrix were virtually homogeneous at several locations both upgradient of and inside the NAPL source zone. Furthermore, the NAPL concentration obtained from the Radon Deficit Factor agrees reasonably with the results derived from direct sampling and chemical analysis of soil samples taken from the residual NAPL source zone. The field results of this study confirmed the general applicability of groundwater radon to detect residual NAPL source zone

Reactive dispersive contaminant transport in coastal aquifers: Numerical simulation of a reactive Henry problem

KAUST Repository

Nick, H.M.

2013-02-01

The reactive mixing between seawater and terrestrial water in coastal aquifers influences the water quality of submarine groundwater discharge. While these waters come into contact at the seawater groundwater interface by density driven flow, their chemical components dilute and react through dispersion. A larger interface and wider mixing zone may provide favorable conditions for the natural attenuation of contaminant plumes. It has been claimed that the extent of this mixing is controlled by both, porous media properties and flow conditions. In this study, the interplay between dispersion and reactive processes in coastal aquifers is investigated by means of numerical experiments. Particularly, the impact of dispersion coefficients, the velocity field induced by density driven flow and chemical component reactivities on reactive transport in such aquifers is studied. To do this, a hybrid finite-element finite-volume method and a reactive simulator are coupled, and model accuracy and applicability are assessed. A simple redox reaction is considered to describe the degradation of a contaminant which requires mixing of the contaminated groundwater and the seawater containing the terminal electron acceptor. The resulting degradation is observed for different scenarios considering different magnitudes of dispersion and chemical reactivity. Three reactive transport regimes are found: reaction controlled, reaction-dispersion controlled and dispersion controlled. Computational results suggest that the chemical components\\' reactivity as well as dispersion coefficients play a significant role on controlling reactive mixing zones and extent of contaminant removal in coastal aquifers. Further, our results confirm that the dilution index is a better alternative to the second central spatial moment of a plume to describe the mixing of reactive solutes in coastal aquifers. © 2012 Elsevier B.V.

Recharge processes drive sulfate reduction in an alluvial aquifer contaminated with landfill leachate

Science.gov (United States)

Scholl, M.A.; Cozzarelli, I.M.; Christenson, S.C.

2006-01-01

Natural attenuation of contaminants in groundwater depends on an adequate supply of electron acceptors to stimulate biodegradation. In an alluvial aquifer contaminated with leachate from an unlined municipal landfill, the mechanism of recharge infiltration was investigated as a source of electron acceptors. Water samples were collected monthly at closely spaced intervals in the top 2 m of the saturated zone from a leachate-contaminated well and an uncontaminated well, and analyzed for ??18O, ??2H, non-volatile dissolved organic carbon (NVDOC), SO42-, NO3- and Cl-. Monthly recharge amounts were quantified using the offset of the ??18O or ??2H from the local meteoric water line as a parameter to distinguish water types, as evaporation and methanogenesis caused isotopic enrichment in waters from different sources. Presence of dissolved SO42- in the top 1 to 2??m of the saturated zone was associated with recharge; SO42- averaged 2.2??mM, with maximum concentrations of 15??mM. Nitrate was observed near the water table at the contaminated site at concentrations up to 4.6??mM. Temporal monitoring of ??2H and SO42- showed that vertical transport of recharge carried SO42- to depths up to 1.75??m below the water table, supplying an additional electron acceptor to the predominantly methanogenic leachate plume. Measurements of ??34S in SO42- indicated both SO42- reduction and sulfide oxidation were occurring in the aquifer. Depth-integrated net SO42- reduction rates, calculated using the natural Cl- gradient as a conservative tracer, ranged from 7.5 ?? 10- 3 to 0.61??mM??d- 1 (over various depth intervals from 0.45 to 1.75??m). Sulfate reduction occurred at both the contaminated and uncontaminated sites; however, median SO42- reduction rates were higher at the contaminated site. Although estimated SO42- reduction rates are relatively high, significant decreases in NVDOC were not observed at the contaminated site. Organic compounds more labile than the leachate NVDOC may be

Recharge processes drive sulfate reduction in an alluvial aquifer contaminated with landfill leachate.

Science.gov (United States)

Scholl, Martha A; Cozzarelli, Isabelle M; Christenson, Scott C

2006-08-10

Natural attenuation of contaminants in groundwater depends on an adequate supply of electron acceptors to stimulate biodegradation. In an alluvial aquifer contaminated with leachate from an unlined municipal landfill, the mechanism of recharge infiltration was investigated as a source of electron acceptors. Water samples were collected monthly at closely spaced intervals in the top 2 m of the saturated zone from a leachate-contaminated well and an uncontaminated well, and analyzed for delta(18)O, delta(2)H, non-volatile dissolved organic carbon (NVDOC), SO(4)(2-), NO(3)(-) and Cl(-). Monthly recharge amounts were quantified using the offset of the delta(18)O or delta(2)H from the local meteoric water line as a parameter to distinguish water types, as evaporation and methanogenesis caused isotopic enrichment in waters from different sources. Presence of dissolved SO(4)(2-) in the top 1 to 2 m of the saturated zone was associated with recharge; SO(4)(2-) averaged 2.2 mM, with maximum concentrations of 15 mM. Nitrate was observed near the water table at the contaminated site at concentrations up to 4.6 mM. Temporal monitoring of delta(2)H and SO(4)(2-) showed that vertical transport of recharge carried SO(4)(2-) to depths up to 1.75 m below the water table, supplying an additional electron acceptor to the predominantly methanogenic leachate plume. Measurements of delta(34)S in SO(4)(2-) indicated both SO(4)(2-) reduction and sulfide oxidation were occurring in the aquifer. Depth-integrated net SO(4)(2-) reduction rates, calculated using the natural Cl(-) gradient as a conservative tracer, ranged from 7.5x10(-3) to 0.61 mM.d(-1) (over various depth intervals from 0.45 to 1.75 m). Sulfate reduction occurred at both the contaminated and uncontaminated sites; however, median SO(4)(2-) reduction rates were higher at the contaminated site. Although estimated SO(4)(2-) reduction rates are relatively high, significant decreases in NVDOC were not observed at the contaminated

Diagnostic Tools for Performance Evaluation of Innovative In-Situ Remediation Technologies at Chlorinated Solvent-Contaminated Sites

Science.gov (United States)

2011-11-01

Electronic down-hole sensors with data loggers, or fiber optic sensors, can also provide information on the pore pressure, temperature, conductivity...of a dechlorinating community resulting from in-situ biostimulation in a trichloroethene-contaminated deep, fractured basalt aquifer and comparison to...dechlorinating community resulting from in-situ biostimulation in a trichloroethene-contaminated deep, fractured basalt aquifer and comparison to a

Application of groundwater residence time tracers and broad screening for micro-organic contaminants in the Indo-Gangetic aquifer system

Science.gov (United States)

Lapworth, Dan; Das, Prerona; Mukherjee, Abhijit; Petersen, Jade; Gooddy, Daren; Krishan, Gopal

2017-04-01

Groundwater abstracted from aquifers underlying urban centres across India provide a vital source of domestic water. Abstraction from municipal and private supplies is considerable and growing rapidly with ever increasing demand for water from expanding urban populations. This trend is set to continue. The vulnerability of deeper aquifers (typically >100 m below ground) used for domestic water to contamination migration from often heavily contaminated shallow aquifer systems has not been studies in detail in India. This paper focusses on the occurrence of micro-organic contaminants within sedimentary aquifers beneath urban centres which are intensively pumped for drinking water and domestic use. New preliminary results from a detailed case study undertaken across Varanasi, a city with an estimated population of ca. 1.5 million in Uttar Pradesh. Micro -organic groundwater quality status and evolution with depth is investigated through selection of paired shallow and deep sites across the city. These results are considered within the context of paired groundwater residence time tracers within the top 150m within the sedimentary aquifer system. Groundwater emerging contaminant results are compared with surface water quality from the Ganges which is also used for drinking water supply. Broad screening for >800 micro-organic compounds was undertaken. Age dating tools were employed to constrain and inform a conceptual model of groundwater recharge and contaminant evolution within the sedimentary aquifer system.

Stochastic Management of Non-Point Source Contamination: Joint Impact of Aquifer Heterogeneity and Well Characteristics

Science.gov (United States)

Henri, C. V.; Harter, T.

2017-12-01

Agricultural activities are recognized as the preeminent origin of non-point source (NPS) contamination of water bodies through the leakage of nitrate, salt and agrochemicals. A large fraction of world agricultural activities and therefore NPS contamination occurs over unconsolidated alluvial deposit basins offering soil composition and topography favorable to productive farming. These basins represent also important groundwater reservoirs. The over-exploitation of aquifers coupled with groundwater pollution by agriculture-related NPS contaminant has led to a rapid deterioration of the quality of these groundwater basins. The management of groundwater contamination from NPS is challenged by the inherent complexity of aquifers systems. Contaminant transport dynamics are highly uncertain due to the heterogeneity of hydraulic parameters controlling groundwater flow. Well characteristics are also key uncertain elements affecting pollutant transport and NPS management but quantifying uncertainty in NPS management under these conditions is not well documented. Our work focuses on better understanding the joint impact of aquifer heterogeneity and pumping well characteristics (extraction rate and depth) on (1) the transport of contaminants from NPS and (2) the spatio-temporal extension of the capture zone. To do so, we generate a series of geostatistically equivalent 3D heterogeneous aquifers and simulate the flow and non-reactive solute transport from NPS to extraction wells within a stochastic framework. The propagation of the uncertainty on the hydraulic conductivity field is systematically analyzed. A sensitivity analysis of the impact of extraction well characteristics (pumping rate and screen depth) is also conducted. Results highlight the significant role that heterogeneity and well characteristics plays on management metrics. We finally show that, in case of NPS contamination, the joint impact of regional longitudinal and transverse vertical hydraulic gradients and

Using enteric pathogens to assess sources of fecal contamination in the Silurian Dolomite Aquifer: Preliminary results

Science.gov (United States)

Muldoon, Maureen A; Borchardt, Mark A.; Spencer, Susan K.; Hunt, Randall J.; Owens, David

2018-01-01

The fractured Silurian dolomite aquifer is an important, but vulnerable, source of drinking water in northeast Wisconsin (Sherrill in Geology and ground water in Door County, Wisconsin, with emphasis on contamination potential in the Silurian dolomite, 1978; Bradbury and Muldoon in Hydrogeology and groundwater monitoring of fractured dolomite in the Upper Door Priority Watershed, Door County, Wisconsin, 1992; Muldoon and Bradbury in Assessing seasonal variations in recharge and water quality in the Silurian aquifer in areas with thicker soil cover. p 45, 2010). Areas underlain by the Silurian dolomite aquifer are extremely vulnerable to groundwater contamination from various land-use activities, especially the disposal of human wastewater and dairy manure. Currently there is no consensus as to which source of wastewater generates the greater impact to the aquifer.

Complementing approaches to demonstrate chlorinated solvent biodegradation in a complex pollution plume: mass balance, PCR and compound-specific stable isotope analysis.

OpenAIRE

Courbet Christelle; Rivière Agnès; Jeannottat Simon; Rinaldi Sandro; Hunkeler Daniel; Bendjoudi Hocine; De Marsily Ghislain

2011-01-01

This work describes the use of different complementing methods (mass balance polymerase chain reaction assays and compound specific stable isotope analysis) to demonstrate the existence and effectiveness of biodegradation of chlorinated solvents in an alluvial aquifer. The solvent contaminated site is an old chemical factory located in an alluvial plain in France. As most of the chlorinated contaminants currently found in the groundwater at this site were produced by local industries at vario...

Decontamination of radioactive contaminated protective wear using dry cleaning solvent

International Nuclear Information System (INIS)

Muthiah, Pushpa; Chitra, S.; Paul, Biplob

2013-01-01

Liquid waste generated by conventional decontamination of radioactive contaminated cotton protective wear using detergent affects the chemical treatment of the plant. To reduce the generation of aqueous detergent waste, dry cleaning of cotton protective wear, highly soiled with oil and grease towards decontamination was tried with organic solvents. Mineral turpentine oil (MTO) among various other organic solvents was identified as a suitable organic solvent. As MTO leaves characteristic odour on the cloth, various commercial fragrances for the removal of the odour were tried. Application of the optimised dry cleaning solvent and commercial fragrance was adopted in plant scale operation. (author)

Radon measurements over a natural-gas contaminated aquifer

International Nuclear Information System (INIS)

Palacios, D.; Fusella, E.; Avila, Y.; Salas, J.; Teixeira, D.; Fernández, G.; Salas, A.; Sajo-Bohus, L.; Greaves, E.; Barros, H.; Bolívar, M.; Regalado, J.

2013-01-01

Radon and thoron concentrations in soil pores in a gas production region of the Anzoategui State, Venezuela, were determined by active and passive methods. In this region, water wells are contaminated by natural gas and gas leaks exist in the nearby river. Based on soil gas Radon data surface hydrocarbon seeps were identified. Radon and thoron concentration maps show anomalously high values near the river gas leaks decreasing in the direction of water wells where natural gas is also detected. The area where the highest concentrations of 222 Rn were detected seems to indicate the surface projection of the aquifer contaminated with natural gas. The Radon/Thoron ratio revealed a micro-localized anomaly, indicating the area where the gas comes from deep layers of the subsoil. The radon map determined by the passive method showed a marked positive anomaly around abandoned gas wells. The high anomalous Radon concentration localized near the trails of ascending gas bubbles at the river indicates the zone trough where natural gases are ascending with greater ease, associated with a deep geological fault, being this the main source of methane penetration into the aquifer. It is suggested that the source of the natural gas may be due to leaks at deep sites along the structure of some of the abandoned wells located at the North-East of the studied area. - Highlights: ► High Radon/Thoron ratios were localized near the natural-gas emanations in a river. ► Natural gases are ascending trough a deep geological fault. ► Apparently, the radon anomaly shows the site where natural gas enters the aquifer. ► Natural gas source may be related to leaks in the structure of abandoned gas wells

Design and construction of an interceptor system for radioactively contaminated solvent

International Nuclear Information System (INIS)

Weiss, T.G. Jr.; Blickwedehl, R.R.

1991-01-01

During the conduct of fuel reprocessing operations at the Western New York Nuclear Service Center from 1966 to 1972, the site operator disposed of spent solvent by shallow land burial in the area used for disposal of solid radioactive waste. The spent solvent was placed in twenty-two 3785 liter (1000-gallon) steel tanks which were then placed in eight 6-meter-deep burial holes. With the passage of time groundwater entered the tanks displacing the solvent (a mixture of tributyl phosphate and n-dodecane) and allowing it to enter the surrounding groundwater system. The solvent, which is lighter than water, floated to the surface of the groundwater within the burial holes and began to migrate laterally through cracks caused by weathering. In 1983, after the US Department of Energy (DOE) initiated efforts for the West Valley Demonstration Project (WVDP), trace amounts of solvent were encountered in a monitoring well near the perimeter of the burial area. Since the initial discovery, extensive studies and continued monitoring have been conducted of the solvent migration. In the fall of 1989, this monitoring showed evidence of further on-site migration of the solvent within the disposal area. In response, the DOE authorized West Valley Nuclear Services Company, Inc. (WVNS) to proceed with the design and construction of a trench system to intercept the flow of solvent and prevent it from discharging to nearby streams. Since the solvent and the contaminated groundwater samples taken in the area exhibited high levels of Iodine-129 in an organic complex, it was necessary to construct a pretreatment facility. An important aspect of the trench construction was the management of contaminated soil and construction water. Contaminated soils were placed into storage containers and held for future treatment and disposal. All water pumped from the trench during construction was stored in large bladder tanks, analyzed for hazardous constituents, and upon finding none, was discharged

Contamination of wells completed in the Roubidoux aquifer by abandoned zinc and lead mines, Ottawa County, Oklahoma

Science.gov (United States)

Christenson, Scott C.

1995-01-01

The Roubidoux aquifer in Ottawa County Oklahoma is used extensively as a source of water for public supplies, commerce, industry, and rural water districts. Water in the Roubidoux aquifer in eastern Ottawa County has relatively low dissolved-solids concentrations (less than 200 mg/L) with calcium, magnesium, and bicarbonate as the major ions. The Boone Formation is stratigraphically above the Roubidoux aquifer and is the host rock for zinc and lead sulfide ores, with the richest deposits located in the vicinity of the City of Picher. Mining in what became known as the Picher mining district began in the early 1900's and continued until about 1970. The water in the abandoned zinc and lead mines contains high concentrations of calcium, magnesium, bicarbonate, sulfate, fluoride, cadmium, copper, iron, lead, manganese, nickel, and zinc. Water from the abandoned mines is a potential source of contamination to the Roubidoux aquifer and to wells completed in the Roubidoux aquifer. Water samples were collected from wells completed in the Roubidoux aquifer in the Picher mining district and from wells outside the mining district to determine if 10 public supply wells in the mining district are contaminated. The chemical analyses indicate that at least 7 of the 10 public supply wells in the Picher mining district are contaminated by mine water. Application of the Mann-Whitney test indicated that the concentrations of some chemical constituents that are indicators of mine-water contamination are different in water samples from wells in the mining area as compared to wells outside the mining area. Application of the Wilcoxon signed-rank test showed that the concentrations of some chemical constituents that are indicators of mine-water contamination were higher in current (1992-93) data than in historic (1981-83) data, except for pH, which was lower in current than in historic data. pH and sulfate, alkalinity, bicarbonate, magnesium, iron, and tritium concentrations consistently

Biodegradation: Updating the Concepts of Control for Microbial Cleanup in Contaminated Aquifers

DEFF Research Database (Denmark)

Meckenstock, Rainer U.; Elsner, Martin; Griebler, Christian

2015-01-01

Biodegradation is one of the most favored and sustainable means of removing organic pollutants from contaminated aquifers but the major steering factors are still surprisingly poorly understood. Growing evidence questions some of the established concepts for control of biodegradation. Here, we...... on the controls of biodegradation in contaminant plumes. These include the plume fringe concept, transport limitations, and transient conditions as currently underestimated processes affecting biodegradation....

Techniques for Source Zone and Plume Characterization of Tetrachloroethene in Fractured Limestone Aquifers

DEFF Research Database (Denmark)

Fjordbøge, Annika Sidelmann; Mosthaf, Klaus; Janniche, Gry S.

Characterization of chlorinated solvents in fractured limestone aquifers is essential for proper development of site specific conceptual models and subsequent risk assessment and remediation. High resolution characterization is challenged by the difficulties involved in collection of intact core...... an improved conceptual understanding of contaminant transport. At both sites limestone cores were collected with significant core losses. The discrete quantification of chlorinated solvents in the retrieved limestone cores was compared to different FLUTe technologies at the DNAPL site and passive and active...... distribution compared to the data obtained by quantification of chlorinated solvents in the limestone cores....

In situ remediation of chlorinated solvent-contaminated groundwater using ZVI/organic carbon amendment in China: field pilot test and full-scale application.

Science.gov (United States)

Yang, Jie; Meng, Liang; Guo, Lin

2018-02-01

Chlorinated solvents in groundwater pose threats to human health and the environment due to their carcinogenesis and bioaccumulation. These problems are often more severe in developing countries such as China. Thus, methods for chlorinated solvent-contaminated groundwater remediation are urgently needed. This study presents a technique of in situ remediation via the direct-push amendment injection that enhances the reductive dechlorination of chlorinated solvents in groundwater in the low-permeability aquifer. A field-based pilot test and a following real-world, full-scale application were conducted at an active manufacturing facility in Shanghai, China. The chlorinated solvents found at the clay till site included 1,1,1-trichloroethane (1,1,1-TCA), 1,1-dichloroethane (1,1-DCA), 1,1-dichloroethylene (1,1-DCE), vinyl chloride (VC), and chloroethane (CA). A commercially available amendment (EHC ® , Peroxychem, Philadelphia, PA) combining zero-valent iron and organic carbon was used to treat the above pollutants. Pilot test results showed that direct-push EHC injection efficiently facilitated the in situ reductive remediation of groundwater contaminated with chlorinated solvents. The mean removal rates of 1,1,1-TCA, 1,1-DCA, and 1,1-DCE at 270 days post-injection were 99.6, 99.3, and 73.3%, respectively, which were obviously higher than those of VC and CA (42.3 and 37.1%, respectively). Clear decreases in oxidation-reduction potential and dissolved oxygen concentration, and increases in Fe 2+ and total organic carbon concentration, were also observed during the monitoring period. These indicate that EHC promotes the anaerobic degradation of chlorinated hydrocarbons primarily via long-term biological reductive dechlorination, with instant chemical reductive dechlorination acting as a secondary pathway. The optimal effective time of EHC injection was 0-90 days, and its radius of influence was 1.5 m. In full-scale application, the maximum concentrations of 1,1,1-TCA

Effects of natural and human factors on groundwater quality of basin-fill aquifers in the southwestern United States-conceptual models for selected contaminants

Science.gov (United States)

Bexfield, Laura M.; Thiros, Susan A.; Anning, David W.; Huntington, Jena M.; McKinney, Tim S.

2011-01-01

As part of the U.S. Geological Survey National Water-Quality Assessment (NAWQA) Program, the Southwest Principal Aquifers (SWPA) study is building a better understanding of the factors that affect water quality in basin-fill aquifers in the Southwestern United States. The SWPA study area includes four principal aquifers of the United States: the Basin and Range basin-fill aquifers in California, Nevada, Utah, and Arizona; the Rio Grande aquifer system in New Mexico and Colorado; and the California Coastal Basin and Central Valley aquifer systems in California. Similarities in the hydrogeology, land- and water-use practices, and water-quality issues for alluvial basins within the study area allow for regional analysis through synthesis of the baseline knowledge of groundwater-quality conditions in basins previously studied by the NAWQA Program. Resulting improvements in the understanding of the sources, movement, and fate of contaminants are assisting in the development of tools used to assess aquifer susceptibility and vulnerability.This report synthesizes previously published information about the groundwater systems and water quality of 15 information-rich basin-fill aquifers (SWPA case-study basins) into conceptual models of the primary natural and human factors commonly affecting groundwater quality with respect to selected contaminants, thereby helping to build a regional understanding of the susceptibility and vulnerability of basin-fill aquifers to those contaminants. Four relatively common contaminants (dissolved solids, nitrate, arsenic, and uranium) and two contaminant classes (volatile organic compounds (VOCs) and pesticide compounds) were investigated for sources and controls affecting their occurrence and distribution above specified levels of concern in groundwater of the case-study basins. Conceptual models of factors that are important to aquifer vulnerability with respect to those contaminants and contaminant classes were subsequently formed. The

Use of aqueous and solvent extraction to assess risk and bioavailability of contaminated soil

International Nuclear Information System (INIS)

Bordelon, N.; Huebner, H.; Washburn, K.; Donnelly, K.C.

1995-01-01

Contaminated media at Superfund sites typically consist of complex mixtures of organic and inorganic chemicals. These mixtures are difficult to characterize, both analytically and toxicologically, especially the complex mixtures of polycyclic aromatic hydrocarbons. The current approach to risk assessment assumes that all contaminants in the soil are available for human exposure. EPA protocol uses solvent extraction to remove chemicals from the soil as a basis for estimating risk to the human population. However, contaminants that can be recovered with a solvent extract may not represent chemicals that are available for exposure. A system using aqueous extraction provides a more realistic picture of what chemicals are bioavailable through leaching and ingestion. A study was conducted with coal tar contaminated soil spiked with benzo(a)pyrene, and trinitrotoluene. Samples were extracted with hexane:acetone and water titrated to pH 2 and pH 7. HPLC analysis demonstrated up to 35% and 29% recovery of contaminants from aqueous extracts with an estimated cancer risk one order of magnitude less than that for solvent extracts. Analysis using the Salmonella/microsome assay showed that solvent extracts were genotoxic with metabolic activation while aqueous extracts showed no genotoxicity. These results suggest that aqueous extraction may be useful in determining what contaminants are available for human exposure, as well as what compounds may pose a risk to human health

Both Phosphorus Fertilizers and Indigenous Bacteria Enhance Arsenic Release into Groundwater in Arsenic-Contaminated Aquifers.

Science.gov (United States)

Lin, Tzu-Yu; Wei, Chia-Cheng; Huang, Chi-Wei; Chang, Chun-Han; Hsu, Fu-Lan; Liao, Vivian Hsiu-Chuan

2016-03-23

Arsenic (As) is a human carcinogen, and arsenic contamination in groundwater is a worldwide public health concern. Arsenic-affected areas are found in many places but are reported mostly in agricultural farmlands, yet the interaction of fertilizers, microorganisms, and arsenic mobilization in arsenic-contaminated aquifers remains uncharacterized. This study investigates the effects of fertilizers and bacteria on the mobilization of arsenic in two arsenic-contaminated aquifers. We performed microcosm experiments using arsenic-contaminated sediments and amended with inorganic nitrogenous or phosphorus fertilizers for 1 and 4 months under aerobic and anaerobic conditions. The results show that microcosms amended with 100 mg/L phosphorus fertilizers (dipotassium phosphate), but not nitrogenous fertilizers (ammonium sulfate), significantly increase aqueous As(III) release in arsenic-contaminated sediments under anaerobic condition. We also show that concentrations of iron, manganese, potassium, sodium, calcium, and magnesium are increased in the aqueous phase and that the addition of dipotassium phosphate causes a further increase in aqueous iron, potassium, and sodium, suggesting that multiple metal elements may take part in the arsenic release process. Furthermore, microbial analysis indicates that the dominant microbial phylum is shifted from α-proteobacteria to β- and γ-proteobacteria when the As(III) is increased and phosphate is added in the aquifer. Our results provide evidence that both phosphorus fertilizers and microorganisms can mediate the release of arsenic to groundwater in arsenic-contaminated sediments under anaerobic condition. Our study suggests that agricultural activity such as the use of fertilizers and monitoring phosphate concentration in groundwater should be taken into consideration for the management of arsenic in groundwater.

Evaluation of Different Modeling Approaches to Simulate Contaminant Transport in a Fractured Limestone Aquifer

Science.gov (United States)

Mosthaf, K.; Rosenberg, L.; Balbarini, N.; Broholm, M. M.; Bjerg, P. L.; Binning, P. J.

2014-12-01

It is important to understand the fate and transport of contaminants in limestone aquifers because they are a major drinking water resource. This is challenging because they are highly heterogeneous; with micro-porous grains, flint inclusions, and being heavily fractured. Several modeling approaches have been developed to describe contaminant transport in fractured media, such as the discrete fracture (with various fracture geometries), equivalent porous media (with and without anisotropy), and dual porosity models. However, these modeling concepts are not well tested for limestone geologies. Given available field data and model purpose, this paper therefore aims to develop, examine and compare modeling approaches for transport of contaminants in fractured limestone aquifers. The model comparison was conducted for a contaminated site in Denmark, where a plume of a dissolved contaminant (PCE) has migrated through a fractured limestone aquifer. Multilevel monitoring wells have been installed at the site and available data includes information on spill history, extent of contamination, geology and hydrogeology. To describe the geology and fracture network, data from borehole logs was combined with an analysis of heterogeneities and fractures from a nearby excavation (analog site). Methods for translating the geological information and fracture mapping into each of the model concepts were examined. Each model was compared with available field data, considering both model fit and measures of model suitability. An analysis of model parameter identifiability and sensitivity is presented. Results show that there is considerable difference between modeling approaches, and that it is important to identify the right one for the actual scale and model purpose. A challenge in the use of field data is the determination of relevant hydraulic properties and interpretation of aqueous and solid phase contaminant concentration sampling data. Traditional water sampling has a bias

Assessing the Vulnerability of Public-Supply Wells to Contamination: Floridan Aquifer System Near Tampa, Florida

Science.gov (United States)

Jagucki, Martha L.; Katz, Brian G.; Crandall, Christy A.; Eberts, Sandra M.

2009-01-01

This fact sheet highlights findings from the vulnerability study of a public-supply well in Temple Terrace, Florida, northeast of Tampa. The well selected for study typically produces water at the rate of 700 gallons per minute from the Upper Floridan aquifer. Water samples were collected at the public-supply well and at monitoring wells installed in or near the simulated zone of contribution to the supply well. Samples of untreated water from the public-supply wellhead contained the undesirable constituents nitrate, arsenic, uranium, radon-222, volatile organic compounds (VOCs), and pesticides, although all were detected at concentrations less than established drinking-water standards, where such standards exist. Overall, study findings point to four primary factors that affect the movement and fate of contaminants and the vulnerability of the public-supply well in Temple Terrace: (1) groundwater age (how long ago water entered, or recharged, the aquifer); (2) short-circuiting of contaminated water through sinkholes; (3) natural geochemical processes within the aquifer; and (4) pumping stress. Although the public-supply well is completed in the Upper Floridan aquifer, it produces water with concentrations of nitrate, VOCs, and the natural contaminant radon that are intermediate between the typical composition of water from the Upper Floridan aquifer and that of the overlying surficial aquifer system. Mixing calculations show that the water produced by the public-supply well could consist of upwards of 50 percent water from the surficial aquifer system mixed with water from the Upper Floridan aquifer. Anthropogenically affected water from the surficial aquifer system travels rapidly to depth through sinkholes that must be directly connected to the cavernous zone intersected by the public-supply well (and several other production wells in the region). Such solution features serve as fast pathways to the well and circumvent the natural attenuation of nitrate and

Evaluation of modeling approaches to simulate contaminant transport in a fractured limestone aquifer

DEFF Research Database (Denmark)

Mosthaf, Klaus; Fjordbøge, Annika Sidelmann; Broholm, Mette Martina

in fractured limestone aquifers. The model comparison is conducted for a contaminated site in Denmark, where a plume of dissolved PCE has migrated through a fractured limestone aquifer. Field data includes information on spill history, distribution of the contaminant (multilevel sampling), geology...... and hydrogeology. To describe the geology and fracture system, data from borehole logs and cores was combined with an analysis of heterogeneities and fractures from a nearby excavation and pump test data. We present how field data is integrated into the different model concepts. A challenge in the use of field...... and remediation strategies. Each model is compared with field data, considering both model fit and model suitability. Results show a considerable difference between the approaches, and that it is important to select the right one for the actual modeling purpose. The comparison with data showed how much...

Hydrophysical logging: A new wellbore technology for hydrogeologic and contaminant characterization of aquifers

International Nuclear Information System (INIS)

Pedler, W.H.; Williams, L.L.; Head, C.L.

1992-01-01

In the continuing search for improved groundwater characterization technologies, a new wellbore fluid logging method has recently been developed to provide accurate and cost effective hydrogeologic and contaminant characterization of bedrock aquifers. This new technique, termed hydrophysical logging, provides critical information for contaminated site characterization and water supply studies and, in addition, offers advantages compared to existing industry standards for aquifer characterization. Hydrophysical logging is based on measuring induced electrical conductivity changes in the fluid column of a wellbore by employing advanced downhole water quality instrumentation specifically developed for the dynamic borehole environment. Hydrophysical logging contemporaneously identifies the locations of water bearing intervals, the interval-specific inflow rate during pumping, and in-situ hydrochemistry of the formation waters associated with each producing interval. In addition, by employing a discrete point downhole fluid sampler during hydrophysical logging, this technique provides evaluation of contaminant concentrations and migration of contaminants vertically within the borehole. Recently, hydrophysical logging was applied in a deep bedrock wellbore at an industrial site in New Hampshire contaminated with dense nonaqueous phase liquids (DNAPLs). The results of the hydrophysical logging, conducted as part of a hydrogeologic site investigation and feasibility study, facilitated investigation of the site by providing information which indicated that the contamination had not penetrated into deeper bedrock fractures at concentrations of concern. This information was used to focus the pending Remedial Action Plan and to provide a more cost-effective remedial design

Contamination Control of Freeze Shoe Coring System for Collection of Aquifer Sands

Science.gov (United States)

Homola, K.; van Geen, A.; Spivack, A. J.; Grzybowski, B.; Schlottenmier, D.

2017-12-01

We have developed and tested an original device, the freeze-shoe coring system, designed to recover undisturbed samples of water contained in sand-dominated aquifers. Aquifer sands are notoriously difficult to collect together with porewater from coincident depths, as high hydraulic permeability leads to water drainage and mixing during retrieval. Two existing corer designs were reconfigured to incorporate the freeze-shoe system; a Hydraulic Piston (HPC) and a Rotary (RC) Corer. Once deployed, liquid CO­2 contained in an interior tank is channeled to coils at the core head where it changes phase, rapidly cooling the deepest portion of the core. The resulting frozen core material impedes water loss during recovery. We conducted contamination tests to examine the integrity of cores retrieved during a March 2017 yard test deployment. Perfluorocarbon tracer (PFC) was added to the drill fluid and recovered cores were subsampled to capture the distribution of PFC throughout the core length and interior. Samples were collected from two HPC and one RC core and analyzed for PFC concentrations. The lowest porewater contamination, around 0.01% invasive fluid, occurs in the center of both HPC cores. The greatest contamination (up to 10%) occurs at the disturbed edges where core material contacts drill fluid. There was lower contamination in the core interior than top, bottom, and edges, as well as significantly lower contamination in HPC cores that those recovered with the RC. These results confirm that the freeze-shoe system, proposed for field test deployments in West Bengal, India, can successfully collect intact porewater and sediment material with minimal if any contamination from drill fluid.

Sulfur cycling in contaminated aquifers: What can we learn from oxygen isotopes in sulfate? (Invited)

Science.gov (United States)

Knoeller, K.; Vogt, C.; Hoth, N.

2009-12-01

Bacterial reduction of dissolved sulfate (BSR) is a key process determining the natural attenuation in many contaminated aquifers. For example, in groundwater bodies affected by acid mine drainage (AMD) BSR reduces the contaminant load by producing alkalinity and facilitating a sustainable fixation of sulfur in the sediment. In aquifers contaminated with petroleum hydrocarbons sulfate may act as a terminal electron acceptor for the anaerobic oxidation of the organic contaminants to carbon dioxide and water. Due to the isotope selectivity of sulfate reducing bacteria, BSR shows the most pronounced isotope fractionation within the sulfur cycle. While sulfur displays a straightforward kinetic enrichment in the residual sulfate described by the enrichment factor epsilon (ɛ), the mechanism of oxygen isotope fractionation is still being discussed controversially. Nevertheless, it is agreed on that oxygen isotope exchange between ambient water and residual sulfate occurs during BSR in natural environments. With respect to this potential isotope exchange, the fractionation parameter theta (θ) is introduced instead of the kinetic enrichment factor epsilon (ɛ). The dual isotope system considering both sulfate-sulfur and sulfate-oxygen isotope fractionation and the respective fractionation parameters ɛ and θ provides an excellent tool for the recognition and quantification of BSR. Beyond that, the dual isotope approach may help identify and estimate interfering sulfur transformations such as re-oxidation and disproportionation processes which is especially vital for the understanding of the overall natural attenuation potential of the investigated aquifers. We present two examples from different field studies showing the benefits of applying the combination of sulfur and oxygen isotopes in dissolved sulfate to reveal the details of the sulfur cycle. The first case study is concerned with the evaluation of the potential for BSR in an AMD-affected aquifer close to an

Microbial ecology of a crude oil contaminated aquifer

Science.gov (United States)

Bekins, B.A.; Cozzarelli, I.M.; Warren, E.; Godsy, E.M.

2002-01-01

Detailed microbial analyses of a glacial outwash aquifer contaminated by crude oil provide insights into the pattern of microbial succession from iron reducing to methanogenic in the anaerobic portion of the contaminant plume. We analysed sediments from this area for populations of aerobes, iron reducers, fermenters and methanogens, using the most probable number method. On the basis of the microbial data the anaerobic area can be divided into distinct physiological zones dominated by either iron-reducers or a consortium of fermenters and methanogens. Chemistry and permeability data show that methanogenic conditions develop first in areas of high hydrocarbon flux. Thus, we find methanogens both in high permeability horizons and also where separate-phase crude oil is present in either the saturated or unsaturated zone. Microbial numbers peak at the top of the separate-phase oil suggesting that growth is most rapid in locations with access to both hydrocarbons and nutrients infiltrating from the surface.

Denitrification and dilution along fracture flowpaths influence the recovery of a bedrock aquifer from nitrate contamination

International Nuclear Information System (INIS)

Kim, Jonathan J.; Comstock, Jeff; Ryan, Peter; Heindel, Craig; Koenigsberger, Stephan

2016-01-01

In 2000, elevated nitrate concentrations ranging from 12 to 34 mg/L NO_3−N were discovered in groundwater from numerous domestic bedrock wells adjacent to a large dairy farm in central Vermont. Long-term plots and contours of nitrate vs. time for bedrock wells showed “little/no”, “moderate”, and “large” change patterns that were spatially separable. The metasedimentary bedrock aquifer is strongly anisotropic and groundwater flow is controlled by fractures, bedding/foliation, and basins and ridges in the bedrock surface. Integration of the nitrate concentration vs. time data and the physical and chemical aquifer characterization suggest two nitrate sources: a point source emanating from a waste ravine and a non-point source that encompasses the surrounding fields. Once removed, the point source of NO_3 (manure deposited in a ravine) was exhausted and NO_3 dropped from 34 mg/L to 10 mg/L. Our multidisciplinary methods of aquifer characterization are applicable to groundwater contamination in any complexly-deformed and metamorphosed bedrock aquifer. - Highlights: • Bedrock wells contaminated with nitrates at a dairy farm in Vermont, U.S.A. • Nitrate concentration vs. time patterns for wells were spatially separable. • Multidisciplinary aquifer characterization used physical and chemical methods. • Denitrification dominant over dilution along fracture flowpaths • Conceptual model shows exhaustion of a nitrate point-source over 12 years.

Potential Risks of Freshwater Aquifer Contamination with Geosequestration

Energy Technology Data Exchange (ETDEWEB)

Jackson, Robert

2013-09-30

Substantial leakage of CO{sub 2} from deep geological strata to shallow potable aquifers is likely to be rare, but chemical detection of potential leakage nonetheless remains an integral component of any safe carbon capture and storage system. CO{sub 2} that infiltrates an unconfined freshwater aquifer will have an immediate impact on water chemistry by lowering pH in most cases and by altering the concentration of total dissolved solids. Chemical signatures in affected waters provide an important opportunity for early detection of leaks. In the presence of CO{sub 2}, trace elements such as Mn, Fe, and Ca can increase by an order of magnitude or more above control concentrations within 100 days. Therefore, these and other elements should be monitored along with pH as geochemical markers of potential CO{sub 2} leaks. Dissolved inorganic carbon and alkalinity can also be rapidly responsive to CO{sub 2} and are stable indicators of a leak. Importantly, such changes may be detectable long before direct changes in CO{sub 2} are observed. The experimental results also suggest that the relative severity of the impact of leaks on overlying drinking-water aquifers should be considered in the selection of CO{sub 2} sequestration sites. One primary selection criteria should be metal and metalloid availability, such as uranium and arsenic abundance, to carefully monitor chemical species that could trigger changes above maximum contaminant levels (MCLs). Overall, the risks of leakage from underground CO{sub 2} storage are real but appear to be manageable if systems are closely monitored.

Using artificial sweeteners to identify contamination sources and infiltration zones in a coupled river-aquifer system

Science.gov (United States)

Bichler, Andrea; Muellegger, Christian; Hofmann, Thilo

2014-05-01

In shallow or unconfined aquifers the infiltration of contaminated river water might be a major threat to groundwater quality. Thus, the identification of possible contamination sources in coupled surface- and groundwater systems is of paramount importance to ensure water quality. Micropollutants like artificial sweeteners are promising markers for domestic waste water in natural water bodies. Compounds, such as artificial sweeteners, might enter the aquatic environment via discharge of waste water treatment plants, leaky sewer systems or septic tanks and are ubiquitously found in waste water receiving waters. The hereby presented field study aims at the (1) identification of contamination sources and (2) delineation of infiltration zones in a connected river-aquifer system. River bank filtrate in the groundwater body was assessed qualitatively and quantitatively using a combined approach of hydrochemical analysis and artificial sweeteners (acesulfame ACE) as waste water markers. The investigated aquifer lies within a mesoscale alpine head water catchment and is used for drinking water production. It is hypothesized that a large proportion of the groundwater flux originates from bank filtrate of a nearby losing stream. Water sampling campaigns in March and July 2012 confirmed the occurrence of artificial sweeteners at the investigated site. The municipal waste water treatment plant was identified as point-source for ACE in the river network. In the aquifer ACE was present in more than 80% of the monitoring wells. In addition, water samples were classified according to their hydrochemical composition, identifying two predominant types of water in the aquifer: (1) groundwater influenced by bank filtrate and (2) groundwater originating from local recharge. In combination with ACE concentrations a third type of water could be discriminated: (3) groundwater influence by bank filtrate but infiltrated prior to the waste water treatment plant. Moreover, the presence of ACE

Contaminant transport in the Snake River Plain Aquifer: Phase 1, Part 1: Simple analytical model of individual plumes

International Nuclear Information System (INIS)

Rood, A.S.; Arnett, R.C.; Barraclough, J.T.

1989-05-01

A preliminary, semi-quantitative assessment of the migration of INEL effluents in the Snake River Plain Aquifer (SRPA) was performed. This study focused on past tritium, 129 I, and 90 Sr effluents from the Idaho Chemical Processing Plant (ICPP) and Test Reactor Area (TRA) and carbon tetrachloride from the Radioactive Waste Management Complex (RWMC). The disposal ponds at TRA and the ICPP injection well were the primary means of liquid radioactive waste discharge from the ICPP and TRA. Drums containing solidified chlorinated solvents disposed of at the RWMC were the primary source of carbon tetrachloride. Water samples taken from wells located in the SRPA show detectable quantities of the four contaminants. The predicted radionuclide concentrations exceed drinking water limits in limited areas within the INEL boundaries. Without planned remedial action, carbon tetrachloride is predicted to exceed drinking water limits beyond the site boundaries near the middle of the next century. 16 refs., 23 figs., 3 tabs

Enhanced reductive de-chlorination of a solvent contaminated aquifer through addition and apparent fermentation of cyclodextrin

Science.gov (United States)

Blanford, William James; Pecoraro, Michael Philip; Heinrichs, Rebecca; Boving, Thomas Bernhard

2018-01-01

In a field study, aqueous cyclodextrin (CD) was investigated for its ability to extract chlorinated volatile organic compounds (cVOC), such as trichloroethylene (TCE), 1,1,1-trichloroethane (TCA), and dichloroethene (DCE) through in-situ flushing of a sandy aquifer. After cessation of aquifer flushing, a plume of CD was left. Changes in CD, cVOC, and inorganic terminal electron acceptors (TEAs) (DO, nitrate, sulfate, iron) were monitored in four rounds of wellwater sampling (20, 210, 342, and 425 days after cessation of active pumping). Post-CD flushing VOC levels rebounded (850% for TCE, 190% for TCA, and 53% for DCE) between the first two sampling rounds, apparently due to rate-limited desorption from aquifer media and dissolution from remaining NAPL. However, substantial reduction in the mass of TCE (6.3 to 0.11 mol: 98%) and TCA (2.8 to 0.73 mol: 74%) in groundwater was observed between 210 and 425 days. DCE should primarily be produced from the degradation of TCE and is expected to subsequently degrade to chloroethene. Since DCE levels decreased only slightly (0.23 to 0.17 mol: 26%), its degradation rate should be similar to that produced from the decaying TCE. Cyclodextrin was monitored starting from day 210. The mass of residual CD (as measured by Total Organic Carbon) decreased from 150 mol (day 210) to 66 (day 425) (56% decrease). The naturally anaerobic zone within the aquifer where residual CD mass decreased coincided with a loss of other major potential TEAs: nitrate (97% loss), sulfate (31%) and iron (31%). In other studies, TCE and 1,1,1-TCA have been found to be more energetically favorable TEAs than sulfate and iron and their degradation via reductive dechlorination has been found to be enhanced by the fermentation of carbohydrates. Such processes can explain these observations, but more investigation is needed to evaluate whether residual levels of CD can facilitate the anaerobic degradation of chlorinated VOCs.

Modeling the potential impact of seasonal and inactive multi-aquifer wells on contaminant movement to public water-supply wells

Science.gov (United States)

Johnson, R.L.; Clark, B.R.; Landon, M.K.; Kauffman, L.J.; Eberts, S.M.

2011-01-01

Wells screened across multiple aquifers can provide pathways for the movement of surprisingly large volumes of groundwater to confined aquifers used for public water supply (PWS). Using a simple numerical model, we examine the impact of several pumping scenarios on leakage from an unconfined aquifer to a confined aquifer and conclude that a single inactive multi-aquifer well can contribute nearly 10% of total PWS well flow over a wide range of pumping rates. This leakage can occur even when the multi-aquifer well is more than a kilometer from the PWS well. The contribution from multi-aquifer wells may be greater under conditions where seasonal pumping (e.g., irrigation) creates large, widespread downward hydraulic gradients between aquifers. Under those conditions, water can continue to leak down a multi-aquifer well from an unconfined aquifer to a confined aquifer even when those multi-aquifer wells are actively pumped. An important implication is that, if an unconfined aquifer is contaminated, multi-aquifer wells can increase the vulnerability of a confined-aquifer PWS well.

Uranium contamination in the Great Miami Aquifer at the Fernald Environmental Management Project, Fernald, Ohio

International Nuclear Information System (INIS)

Sidle, W.C.

1996-01-01

Ground-water investigations at a former US Department of Energy nuclear weapons complex near Fernald, in southwestern Ohio, included the delineation of uranium contamination above the USEPA proposed drinking water standard of 20 microg/l. Contamination occurs in a buried valley and has migrated >1.5 km south-southeast of the facility boundary. Flooring of the plume(s) appears to be ≅ 32 m below the water table of the Great Miami Aquifer. U 6+ predominates in the modeled U-O 2 -CO 2 -H 2 O system and U retardation decreases at depth. U 234 /U 238 disequilibria analyses complement hydrogeologic studies which suggest that U leakage through the clayey till cap is less significant than the predominant transport pathway of infiltration via drainage channels incised into the aquifer

Assessment of microbial in situ activity in contaminated aquifers

Energy Technology Data Exchange (ETDEWEB)

Kaestner, M. [UFZ-Umweltforschungszentrum Leipzig-Halle GmbH, Department Bioremediation, Permoserstrasse 15, 04318 Leipzig (Germany); Fischer, A.; Nijenhuis, I.; Stelzer, N.; Bombach, P.; Richnow, H.H. [UFZ-Umweltforschungszentrum Leipzig-Halle GmbH, Department Isotopenbiogeochemie, Permoserstrasse 15, 04318 Leipzig (Germany); Geyer, R. [UFZ-Umweltforschungszentrum Leipzig-Halle GmbH, Department Umweltmikrobiologie, Permoserstrasse 15, 04318 Leipzig (Germany); Tebbe, C.C. [Institut fuer Agraroekologie, Bundesforschungsanstalt fuer Landwirtschaft (FAL), D-38116 Braunschweig (Germany)

2006-06-15

Microbial ecologists and environmental engineers share the interest in identifying the key microorganisms responsible for compound turnover in the environment and in estimating the respective transformation rates. For the successful application of Natural Attenuation processes, a reliable assessment of the in situ turnover of a contaminant in an aquifer is essential. Here, we review and present new details of two recently developed approaches concerning the assessment of in situ biodegradation: (i) determination of biodegradation caused by microbial metabolism in a contamination plume by stable isotope fractionation analysis (SIFA) and (ii) determination of the actual degradation under the respective environmental conditions in the aquifer by using in situ microcosms (BACTRAPS registered) amended with {sup 13}C-labeled substrates as tracer compounds. Based on stable isotope fractionation analysis, the degradation occurring under anoxic biogeochemical conditions at a respective site can be calculated for the entire plume. This has been shown for benzene and toluene at the Zeitz site and partly for chlorobenzene at the Bitterfeld site. By use of the in situ microcosm approach with {sup 13}C-labeled compounds, the microbial in situ degradation under strictly anaerobic conditions could be proven for benzene and toluene in Zeitz and for chlorobenzene in Bitterfeld. The transformation of {sup 13}C-carbon of the labeled substrate into microbial fatty acids confirmed the assimilation of the pollutant resulting in the formation of biomass. In addition, metabolites such as benzylsuccinic acid were found in the toluene-amended microcosms indicating anaerobic degradation of toluene. This result corresponds to the geochemical conditions found at the field site and therefore, the microcosm approach with {sup 13}C-labeled compounds can be used to assign the predominant in situ degradation pathways in a contaminated aquifer. Since fatty acids profiles alone are often too

Consequences of preferential flow in cracking clay soils for contamination-risk of shallow aquifers

NARCIS (Netherlands)

Oostindie, K.; Bronswijk, J.J.B.

1995-01-01

A method is presented to asses the contamination risk of aquifers covered with cracking clay soils, with special emphasis on preferential flow through shrinkage cracks. A water extraction area was divided into units with homogeneous soil types and hydrological conditions. For each unit, a

Simulation of ground-water flow in the St. Peter aquifer in an area contaminated by coal-tar derivatives, St. Louis Park, Minnesota. Water Resources Investigation

International Nuclear Information System (INIS)

Lorenz, D.L.; Stark, J.R.

1990-01-01

A model constructed to simulate ground-water flow in part of the Prairie du Chien-Jordan and St. Peter aquifers, St. Louis Park, Minnesota, was used to test hypotheses about the movement of ground water contaminated with coal-tar derivatives and to simulate alternatives for reducing the downgradient movement of contamination in the St. Peter aquifer. The model, constructed for a previous study, was applied to simulate the effects of current ground-water withdrawals on the potentiometric surface of the St. Peter aquifer. Model simulations predict that the multiaquifer wells have the potential to limit downgradient migration of contaminants in the St. Peter aquifer caused by cones of depression created around the multiaquifer wells. Differences in vertical leakage to the St. Peter aquifer may exist in areas of bedrock valleys. Model simulations indicate that these differences are not likely to affect significantly the general patterns of ground-water flow

Thermally enhanced bioremediation of a gasoline-contaminated aquifer using toluene oxidizing bacteria

International Nuclear Information System (INIS)

Deeb, R.; Alvarez-Cohen, L.

1994-01-01

The combined application of steam injection and vacuum extraction has proved to be very effective for the in situ remediation of a gasoline contaminated aquifer. It is expected that the steam treated zone with its near-sterile nature, increased temperature, and decreased level of contaminant concentration will provide a superior environment for enhanced bioremediation, and will favor the survival of an introduced microbial culture for the destruction of residual gasoline hydrocarbons and especially BTEX compounds (Benzene, Toluene, Ethyl benzene, and Xylene). A mixed microbial culture seeded from the pre-steamed aquifer material was enriched in a laboratory chemostat on toluene, a major gasoline aromatic. Studies were conducted to determine the optimal conditions for microbial growth and activity. Growth rate studies conducted at different temperatures revealed that cell growth was optimal at 35 C, a temperature at which the aquifer can be maintained using the existing steam injection wells. The enriched culture was shown to degrade all BTEX compounds successfully both individually and in mixtures. Substrate toxicity was observed for some of the gasoline aromatics but at concentration levels well above those found in groundwater. When cells were exposed to mixtures of BTEX compounds, the biodegradation of xylene, the most recalcitrant aromatic among BTEX compounds, was stimulated. When cells were exposed to gasoline, BTEX degradation proceeded with no apparent inhibition by gasoline aliphatics; little aliphatic degradation took place, however, suggesting the absence of monooxygenase enzymes in the mixed culture. In mixtures of both toluene and propane enriched cultures, only dioxygenase activity was observed

Fingerprinting groundwater pollution in catchments with contrasting contaminant sources using microorganic compounds.

Science.gov (United States)

Stuart, Marianne E; Lapworth, Dan J; Thomas, Jenny; Edwards, Laura

2014-01-15

Evaluating the occurrence of microorganics helps to understand sources and processes which may be controlling the transport and fate of emerging contaminants (ECs). A study was carried out at the contrasting instrumented environmental observatory sites at Oxford, on the peri-urban floodplain gravel aquifer of the River Thames and Boxford, in the rural valley of the River Lambourn on the chalk aquifer, in Southern England to explore the use of ECs to fingerprint contaminant sources and flow pathways in groundwater. At Oxford compounds were typical of a local waste tip plume (not only plasticisers and solvents but also barbiturates and N,N-diethyl-m-toluamide (DEET)) and of the urban area (plasticisers and mood-enhancing drugs such as carbamazepine). At Boxford the results were different with widespread occurrence of agricultural pesticides, their metabolites and the solvent trichloroethene, as well as plasticisers, caffeine, butylated food additives, DEET, parabens and trace polyaromatic hydrocarbons (PAHs). Groups of compounds used in pharmaceuticals and personal care products of different provenance in the environment could be distinguished, i) historical household and medical waste, ii) long-term household usage persistent in groundwater and iii) current usage and contamination from surface water. Co-contaminant and degradation products can also indicate the likely source of contaminants. A cocktail of contaminants can be used as tracers to provide information on catchment pathways and groundwater/surface water interactions. A prominent feature in this study is the attenuation of many EC compounds in the hyporheic zone. © 2013.

A convenient method for estimating the contaminated zone of a subsurface aquifer resulting from radioactive waste disposal into ground

International Nuclear Information System (INIS)

Fukui, Masami; Katsurayama, Kousuke; Uchida, Shigeo.

1981-01-01

Studies were conducted to estimate the contamination spread resulting from the radioactive waste disposal into a subsurface aquifer. A general equation, expressing the contaminated zone as a function of radioactive decay, the physical and chemical parameters of soil is presented. A distribution coefficient was also formulated which can be used to judge the suitability of a site for waste disposal. Moreover, a method for predicting contaminant concentration in groundwater at a site boundary is suggested for a heterogeneous media where the subsurface aquifer has different values of porosity, density, flow velocity, distribution coefficient and so on. A general equation was also developed to predict the distribution of radionuclides resulting from the disposal of a solid waste material. The distributions of contamination was evaluated for 90 Sr and 239 Pu which obey a linear adsorption model and a first order kinetics respectively. These equations appear to have practical utility for easily estimating groundwater contamination. (author)

Nitrate Contamination of Deep Aquifers in the Salinas Valley, California

Science.gov (United States)

Moran, J. E.; Esser, B. K.; Hillegonds, D. J.; Holtz, M.; Roberts, S. K.; Singleton, M. J.; Visser, A.; Kulongoski, J. T.; Belitz, K.

2011-12-01

The Salinas Valley, known as 'the salad bowl of the world', has been an agricultural center for more than 100 years. Irrigated row crops such as lettuce and strawberries dominate both land use and water use. Groundwater is the exclusive supply for both irrigation and drinking water. Some irrigation wells and most public water supply wells in the Salinas Valley are constructed to draw water from deep portions of the aquifer system, where contamination by nitrate is less likely than in the shallow portions of the aquifer system. However, a number of wells with top perforations greater than 75 m deep, screened below confining or semi-confining units, have nitrate concentrations greater than the Maximum Contaminant Limit (MCL) of 45 mg/L as NO3-. This study uses nitrate concentrations from several hundred irrigation, drinking water, and monitoring wells (Monterey County Water Resources Agency, 1997), along with tritium-helium groundwater ages acquired at Lawrence Livermore National Laboratory through the State of California Groundwater Monitoring and Assessment (GAMA) program (reported in Kulongoski et al., 2007 and in Moran et al., in press), to identify nitrate 'hot spots' in the deep aquifer and to examine possible modes of nitrate transport to the deep aquifer. In addition, observed apparent groundwater ages are compared with the results of transport simulations that use particle tracking and a stochastic-geostatistical framework to incorporate aquifer heterogeneity to determine the distribution of travel times from the water table to each well (Fogg et al., 1999). The combined evidence from nitrate, tritium, tritiogenic 3He, and radiogenic 4He concentrations, reveals complex recharge and flow to the capture zone of the deep drinking water wells. Widespread groundwater pumping for irrigation accelerates vertical groundwater flow such that high nitrate groundwater reaches some deep drinking water wells. Deeper portions of the wells often draw in water that recharged

Multi-isotope (carbon and chlorine) analysis for fingerprinting and site characterization at a fractured bedrock aquifer contaminated by chlorinated ethenes

Energy Technology Data Exchange (ETDEWEB)

Palau, Jordi, E-mail: jordi.palau@unine.ch [Departament de Cristal.lografia, Mineralogia i Dipòsits Minerals, Facultat de Geologia, Universitat de Barcelona, Martí i Franquès, s/n 08028 Barcelona (Spain); Marchesi, Massimo [Departament de Cristal.lografia, Mineralogia i Dipòsits Minerals, Facultat de Geologia, Universitat de Barcelona, Martí i Franquès, s/n 08028 Barcelona (Spain); Department of Earth and Environmental Sciences, University of Waterloo, Waterloo, Ontario N2L 3G1 (Canada); Chambon, Julie C.C. [Department of Environmental Engineering, Technical University of Denmark, 2800 Lyngby (Denmark); Aravena, Ramon [Department of Earth and Environmental Sciences, University of Waterloo, Waterloo, Ontario N2L 3G1 (Canada); Canals, Àngels [Departament de Cristal.lografia, Mineralogia i Dipòsits Minerals, Facultat de Geologia, Universitat de Barcelona, Martí i Franquès, s/n 08028 Barcelona (Spain); Binning, Philip J.; Bjerg, Poul L. [Department of Environmental Engineering, Technical University of Denmark, 2800 Lyngby (Denmark); Otero, Neus; Soler, Albert [Departament de Cristal.lografia, Mineralogia i Dipòsits Minerals, Facultat de Geologia, Universitat de Barcelona, Martí i Franquès, s/n 08028 Barcelona (Spain)

2014-03-01

The use of compound specific multi-isotope approach (C and Cl) in the characterization of a chlorinated ethenes contaminated fractured aquifer allows the identification of several sources and contaminant plumes, as well as the occurrence of biodegradation and mixing processes. The study site is located in Spain with contamination resulting in groundwater concentrations of up to 50 mg/L of trichloroethene (TCE), the most abundant chlorinated ethene, and 7 mg/L of tetrachloroethene (PCE). The potential sources of contamination including abandoned barrels, an underground tank, and a disposal lagoon, showed a wide range in δ{sup 13}C values from − 15.6 to − 40.5‰ for TCE and from − 18.5 to − 32.4‰ for PCE, allowing the use of isotope fingerprinting for tracing of the origin and migration of these contaminants in the aquifer. In contrast, there is no difference between the δ{sup 37}Cl values for TCE in the contaminant sources, ranging from + 0.53 to + 0.66‰. Variations of δ{sup 37}Cl and δ{sup 13}C in the different contaminant plumes were used to investigate the role of biodegradation in groundwater. Moreover, the isotopic data were incorporated into a reactive transport model for determination of whether the isotope pattern observed downstream from the tank's source could be explained by the simultaneous effect of mixing and biodegradation. The results demonstrate that a multi-isotope approach is a valuable tool for characterization of complex sites such as fractured bedrock aquifer contaminated by multiple sources, providing important information which can be used by consultants and site managers to prioritize and design more successful remediation strategies. - Highlights: • Origin and fate of CAHs in groundwater by means of multi CSIA ({sup 13}C,{sup 35}Cl) survey • Innovative/new approach tested in a fractured bedrock site • Differentiation of distinct CAH sources • Biodegradation and source mixing recognition in the aquifer.

Multi-isotope (carbon and chlorine) analysis for fingerprinting and site characterization at a fractured bedrock aquifer contaminated by chlorinated ethenes

International Nuclear Information System (INIS)

Palau, Jordi; Marchesi, Massimo; Chambon, Julie C.C.; Aravena, Ramon; Canals, Àngels; Binning, Philip J.; Bjerg, Poul L.; Otero, Neus; Soler, Albert

2014-01-01

The use of compound specific multi-isotope approach (C and Cl) in the characterization of a chlorinated ethenes contaminated fractured aquifer allows the identification of several sources and contaminant plumes, as well as the occurrence of biodegradation and mixing processes. The study site is located in Spain with contamination resulting in groundwater concentrations of up to 50 mg/L of trichloroethene (TCE), the most abundant chlorinated ethene, and 7 mg/L of tetrachloroethene (PCE). The potential sources of contamination including abandoned barrels, an underground tank, and a disposal lagoon, showed a wide range in δ 13 C values from − 15.6 to − 40.5‰ for TCE and from − 18.5 to − 32.4‰ for PCE, allowing the use of isotope fingerprinting for tracing of the origin and migration of these contaminants in the aquifer. In contrast, there is no difference between the δ 37 Cl values for TCE in the contaminant sources, ranging from + 0.53 to + 0.66‰. Variations of δ 37 Cl and δ 13 C in the different contaminant plumes were used to investigate the role of biodegradation in groundwater. Moreover, the isotopic data were incorporated into a reactive transport model for determination of whether the isotope pattern observed downstream from the tank's source could be explained by the simultaneous effect of mixing and biodegradation. The results demonstrate that a multi-isotope approach is a valuable tool for characterization of complex sites such as fractured bedrock aquifer contaminated by multiple sources, providing important information which can be used by consultants and site managers to prioritize and design more successful remediation strategies. - Highlights: • Origin and fate of CAHs in groundwater by means of multi CSIA ( 13 C, 35 Cl) survey • Innovative/new approach tested in a fractured bedrock site • Differentiation of distinct CAH sources • Biodegradation and source mixing recognition in the aquifer

Comparison of different modeling approaches to simulate contaminant transport in a fractured limestone aquifer

DEFF Research Database (Denmark)

Mosthaf, Klaus; Rosenberg, L.; Balbarini, Nicola

. Given available field data and model purpose, this paper therefore aims to develop, examine and compare modeling approaches for transport of contaminants in fractured limestone aquifers. The model comparison was conducted for a contaminated site in Denmark, where a plume of a dissolved contaminant (PCE...... was combined with an analysis of heterogeneities and fractures from a nearby excavation (analog site). Methods for translating the geological information and fracture mapping into each of the model concepts were examined. Each model was compared with available field data, considering both model fit...... of field data is the determination of relevant hydraulic properties and interpretation of aqueous and solid phase contaminant concentration sampling data. Traditional water sampling has a bias towards fracture sampling, however concentrations in the limestone matrix are needed for assessing contaminant...

Preliminary Study Contamination of Organochlorine Pesticide (Heptachlor) and Heavy Metal (Arsenic) in Shallow Groundwater Aquifer of Semarang Coastal Areas

Science.gov (United States)

Rochaddi, Baskoro; Adhi Suryono, Chrisna; Atmodjo, Warsito; Satriadi, Alfi

2018-02-01

The present study was conducted to assess the level of pesticide and heavy metal contamination in shallow aquifer of Semarang coastal areas. Results indicated that Heptachlor and Arsenic were detected in the water samples in the range 0.023-0.055 μg L-1 and 0,03-1,63 μg L-1, respectively. Compared to the standard limits of the organochlorine contents in the water sample by World Health Organization (WHO) limits and Indonesian Drinking and Domestic Water Quality Standard for Ground Water (IWQS), groundwater of Semarang Coastal Areas was contaminated with pesticide and heavy metal. This study has proven the presence of organochlorine and heavy metal contamination of some shallow aquifer supplies in the coastal areas of Semarang.

Fluorescence in situ hybridization (CARD-FISH) of microorganisms in hydrocarbon contaminated aquifer sediment samples.

Science.gov (United States)

Tischer, Karolin; Zeder, Michael; Klug, Rebecca; Pernthaler, Jakob; Schattenhofer, Martha; Harms, Hauke; Wendeberg, Annelie

2012-12-01

Groundwater ecosystems are the most important sources of drinking water worldwide but they are threatened by contamination and overexploitation. Petroleum spills account for the most common source of contamination and the high carbon load results in anoxia and steep geochemical gradients. Microbes play a major role in the transformation of petroleum hydrocarbons into less toxic substances. To investigate microbial populations at the single cell level, fluorescence in situ hybridization (FISH) is now a well-established technique. Recently, however, catalyzed reporter deposition (CARD)-FISH has been introduced for the detection of microbes from oligotrophic environments. Nevertheless, petroleum contaminated aquifers present a worst case scenario for FISH techniques due to the combination of high background fluorescence of hydrocarbons and the presence of small microbial cells caused by the low turnover rates characteristic of groundwater ecosystems. It is therefore not surprising that studies of microorganisms from such sites are mostly based on cultivation techniques, fingerprinting, and amplicon sequencing. However, to reveal the population dynamics and interspecies relationships of the key participants of contaminant degradation, FISH is an indispensable tool. In this study, a protocol for FISH was developed in combination with cell quantification using an automated counting microscope. The protocol includes the separation and purification of microbial cells from sediment particles, cell permeabilization and, finally, CARD-FISH in a microwave oven. As a proof of principle, the distribution of Archaea and Bacteria was shown in 60 sediment samples taken across the contaminant plume of an aquifer (Leuna, Germany), which has been heavily contaminated with several ten-thousand tonnes of petroleum hydrocarbons since World War II. Copyright © 2012 Elsevier GmbH. All rights reserved.

Identification of critical contaminants in wastewater effluent for managed aquifer recharge.

Science.gov (United States)

Yuan, Jie; Van Dyke, Michele I; Huck, Peter M

2017-04-01

Managed aquifer recharge (MAR) using highly treated effluent from municipal wastewater treatment plants has been recognized as a promising strategy for indirect potable water reuse. Treated wastewater effluent can contain a number of residual contaminants that could have adverse effects on human health, and some jurisdictions have regulations in place to govern these. For those that do not, but where reuse may be under consideration, it is of crucial importance to develop a strategy for identifying priority contaminants, which can then be used to understand the water treatment technologies that might be required. In this study, a multi-criteria approach to identify critical contaminants in wastewater effluent for MAR was developed and applied using a case study site located in southern Ontario, Canada. An important aspect of this approach was the selection of representative compounds for each group of contaminants, based on potential for occurrence in wastewater and expected health or environmental impacts. Due to a lack of MAR regulations in Canada, the study first proposed potential recharge water quality targets. Predominant contaminants, potential additional contaminants, and potential emerging contaminants, which together comprise critical contaminants for MAR with reclaimed water, were then selected based on the case study wastewater effluent monitoring data and literature data. This paper proposes an approach for critical contaminant selection, which will be helpful to guide future implementation of MAR projects using wastewater treatment plant effluents. Copyright © 2016 Elsevier Ltd. All rights reserved.

Biotransformation of chlorinated aliphatic solvents in the presence of aromatic compounds under methanogenic conditions

International Nuclear Information System (INIS)

Liang, L.N.; Grbic-Galic, D.

1993-01-01

Transformation of carbon tetrachloride (CT) and tetrachloroethylene (PCE) was studied under methanogenic conditions, in the presence or absence of toluene, ethylbenzene, phenol, and benzoate. Microbial inoculate for the experiments were derived from three groundwater aquifers contaminated by jet fuel or creosote. CT and PCE were reductively dechlorinated in all the examined castes (CT to chloroform [CF]; PCE to trichloroethylene [TCE], trans-1,2-dichloroethylene [DCE], and vinyl chloride [VC]). In the aquifer microcosms, the electron donors used for the reductive transformations were most likely the unidentified organic compounds present on aquifer solids, or storage materials in microorganisms. Alternatively, molecular hydrogen from the anaerobic incubator atmosphere could have been used. The addition of benzoate caused a decrease in rates of dechlorination if benzoate was transformed. Phenol and ethylbenzene were not degraded and did not influence the transformation of CT or PCE. Toluene, in most of the studied cases, had no influence on reductive dechlorination of either CT or PCE. Only in microcosms derived from a JP-4 jet fuel-contaminated aquifer did the anaerobic degradation of toluene occur simultaneously with reductive dechlorination of PCE, suggesting that toluene might possibly have been used as an electron donor for reductive transformation of chlorinated solvents

Mobilization of arsenic and other naturally occurring contaminants in groundwater of the Main Ethiopian Rift aquifers.

Science.gov (United States)

Rango, Tewodros; Vengosh, Avner; Dwyer, Gary; Bianchini, Gianluca

2013-10-01

This study investigates the mechanisms of arsenic (As) and other naturally occurring contaminants (F(-), U, V, B, and Mo) mobilization from Quaternary sedimentary aquifers of the Main Ethiopian Rift (MER) and their enrichment in the local groundwater. The study is based on systematic measurements of major and trace elements as well as stable oxygen and hydrogen isotopes in groundwater, coupled with geochemical and mineralogical analyses of the aquifer rocks. The Rift Valley aquifer is composed of rhyolitic volcanics and Quaternary lacustrine sediments. X-ray fluorescence (XRF) results revealed that MER rhyolites (ash, tuff, pumice and ignimbrite) and sediments contain on average 72 wt. % and 65 wt. % SiO2, respectively. Petrographic studies of the rhyolites indicate predominance of volcanic glass, sanidine, pyroxene, Fe-oxides and plagioclase. The As content in the lacustrine sediments (mean = 6.6 mg/kg) was higher than that of the rhyolites (mean: 2.5 mg/kg). The lacustrine aquifers of the Ziway-Shala basin in the northern part of MER were identified as high As risk zones, where mean As concentration in groundwater was 22.4 ± 33.5 (range of 0.60-190 μg/L) and 54% of samples had As above the WHO drinking water guideline value of 10 μg/L. Field As speciation measurements showed that most of the groundwater samples contain predominantly (~80%) arsenate-As(V) over arsenite-As(III) species. The As speciation together with field data of redox potential (mean Eh = +73 ± 65 mV) and dissolved-O2 (6.6 ± 2.2 mg/L) suggest that the aquifer is predominantly oxidative. Water-rock interactions, including the dissolution of volcanic glass produces groundwater with near-neutral to alkaline pH (range 6.9-8.9), predominance of Na-HCO3 ions, and high concentration of SiO2 (mean: 85.8 ± 11.3 mg/L). The groundwater data show high positive correlation of As with Na, HCO3, U, B, V, and Mo (R(2) > 0.5; p groundwater indicates that Fe-oxides and oxyhydroxides minerals were saturated

Hydrogeology, water quality, and potential for contamination of the Upper Floridan aquifer in the Silver Springs ground-water basin, central Marion County, Florida

Science.gov (United States)

Phelps, G.G.

1994-01-01

The Upper Floridan aquifer, composed of a thick sequence of very porous limestone and dolomite, is the principal source of water supply in the Silver Springs ground-water basin of central Marion County, Florida. The karstic nature of the local geology makes the aquifer susceptible to contaminants from the land surface. Contaminants can enter the aquifer by seepage through surficial deposits and through sinkholes and drainage wells. Potential contaminants include agricultural chemicals, landfill leachates and petroleum products from leaking storage tanks and accidental spills. More than 560 sites of potential contamination sources were identified in the basin in 1990. Detailed investigation of four sites were used to define hydrologic conditions at representative sites. Ground-water flow velocities determined from dye trace studies ranged from about 1 foot per hour under natural flow conditions to about 10 feet per hour under pumping conditions, which is considerably higher than velocities estimated using Darcy's equation for steady-state flow in a porous medium. Water entering the aquifer through drainage wells contained bacteria, elevated concentrations of nutrients, manganese and zinc, and in places, low concentrations of organic compounds. On the basis of results from the sampling of 34 wells in 1989 and 1990, and from the sampling of water entering the Upper Floridan aquifer through drainage wells, there has been no widespread degradation of water quality in the study area. In an area of karst, particularly one in which fracture flow is significant, evaluating the effects from contaminants is difficult and special care is required when interpolating hydrogeologic data from regional studies to a specific. (USGS)

Molecular analysis of microbial community structures in pristine and contaminated aquifers--Field and laboratory microcosm experiments

Science.gov (United States)

Shi, Y.; Zwolinski, M.D.; Schreiber, M.E.; Bahr, J.M.; Sewell, G.W.; Hickey, W.J.

1999-01-01

Molecular Analysis of Microbial Community Structures in Pristine and Contaminated Aquifers: Field and Laboratory Microcosm Experimentsvar callbackToken='531E8ACDB6C8511'; var subCode='asmjournal_sub'; var OAS_sitepage = 'aem.asm.org'; This study used phylogenetic probes in hybridization analysis to (i) determine in situ microbial community structures in regions of a shallow sand aquifer that were oxygen depleted and fuel contaminated (FC) or aerobic and noncontaminated (NC) and (ii) examine alterations in microbial community structures resulting from exposure to toluene and/or electron acceptor supplementation (nitrate). The latter objective was addressed by using the NC and FC aquifer materials for anaerobic microcosm studies in which phylogenetic probe analysis was complemented by microbial activity assays. Domain probe analysis of the aquifer samples showed that the communities were predominantlyBacteria; Eucarya and Archaea were not detectable. At the phylum and subclass levels, the FC and NC aquifer material had similar relative abundance distributions of 43 to 65% β- and γ-Proteobacteria (B+G), 31 to 35% α-Proteobacteria (ALF), 15 to 18% sulfate-reducing bacteria, and 5 to 10% high G+C gram positive bacteria. Compared to that of the NC region, the community structure of the FC material differed mainly in an increased abundance of B+G relative to that of ALF. The microcosm communities were like those of the field samples in that they were predominantly Bacteria (83 to 101%) and lacked detectable Archaea but differed in that a small fraction (2 to 8%) of Eucarya was detected regardless of the treatment applied. The latter result was hypothesized to reflect enrichment of anaerobic protozoa. Addition of nitrate and/or toluene stimulated microbial activity in the microcosms, but only supplementation of toluene alone significantly altered community structures. For the NC material, the dominant subclass shifted from B+G to ALF, while in the FC microcosms 55 to 65

Organic solvents improve hydrocarbon desorption and biodegradation in highly contaminated weathered soils

Energy Technology Data Exchange (ETDEWEB)

Garcia-Rivero, M. [Tecnologico de Estudios Superiores de Ecatepec, Mexico City (Mexico); Saucedo-Casteneda, G.; Gutierrez-Rojas, M. [Autonoma Metropolitan Univ., Mexico City (Mexico). Dept. of Biotechnology

2007-07-15

A toluene-based microbial slurry phase system was used to remediate hydrocarbons (HC) in highly contaminated soil samples collected from a site next to a working refinery in Mexico. Initial HC concentrations of the samples were 237.2 {+-} 16,6 g kg{sup -1} in dry soil. The microbial consortium consisted of 10 different strains in a mineral solution. Non-polar solvents used in the phase system included hexane, benzene, and toluene. Polar solvents included n-butanol, acetone, and methanol. The bioavailability of the HCs was increased using both polar and nonpolar solvents in order to promote desorption from the soil and to enhance overall HC biodegradation. HC desorption was analyzed in an abiotic system. Respiration and residual HCs were examined after a period of 30 days in order to compare the effects of the 2 solvents. The biodegradation extracts were then fractionated in a silica gel column to determine if the solvents actually enhanced the biodegradation of specific HC fractions. The study showed that induced dipole interactions forces resulted when nonpolar molecules were dissolved into a nonpolar solvent. Results for desorption and solubility varied among the 6 solvents. Higher dielectric constants resulted in higher solubility and desorption of HCs for nonpolar solvents, while the opposite effect was observed for polar solvents. It was concluded that toluene produced better biodegradation results than any of the milder solvents. 34 refs., 4 tabs., 1 fig.

Investigation of ethyl lactate as a green solvent for desorption of total petroleum hydrocarbons (TPH) from contaminated soil.

Science.gov (United States)

Jalilian Ahmadkalaei, Seyedeh Pegah; Gan, Suyin; Ng, Hoon Kiat; Abdul Talib, Suhaimi

2016-11-01

Treatment of oil-contaminated soil is a major environmental concern worldwide. The aim of this study is to examine the applicability of a green solvent, ethyl lactate (EL), in desorption of diesel aliphatic fraction within total petroleum hydrocarbons (TPH) in contaminated soil and to determine the associated desorption kinetics. Batch desorption experiments were carried out on artificially contaminated soil at different EL solvent percentages (%). In analysing the diesel range of TPH, TPH was divided into three fractions and the effect of solvent extraction on each fraction was examined. The experimental results demonstrated that EL has a high and fast desorbing power. Pseudo-second order rate equation described the experimental desorption kinetics data well with correlation coefficient values, R 2 , between 0.9219 and 0.9999. The effects of EL percentage, initial contamination level of soil and liquid to solid ratio (L/S (v/w)) on initial desorption rate have also been evaluated. The effective desorption performance of ethyl lactate shows its potential as a removal agent for remediation of TPH-contaminated soil worldwide.

Laboratory and pilot field-scale testing of surfactants for environmental restoration of chlorinated solvent DNAPLs

International Nuclear Information System (INIS)

Jackson, R.E.; Fountain, J.C.

1994-01-01

This project is composed of two phases and has the objective of demonstrating surfactant-enhanced aquifer remediation (SEAR) as a practical remediation technology at DOE sites with ground water contaminated by dense, non-aqueous phase liquids (DNAPLs), in particular, chlorinated solvents. The first phase of this project, Laboratory and Pilot Field Scale Testing, which is the subject of the work so far, involves (1) laboratory experiments to examine the solubilization of multiple component DNAPLs, e.g., solvents such as perchloroethylene (PCE) and trichloroethylene (TCE), by dilute surfactant solutions, and (2) a field test to demonstrate SEAR technology on a small scale and in an existing well

Key players and team play: anaerobic microbial communities in hydrocarbon-contaminated aquifers.

Science.gov (United States)

Kleinsteuber, Sabine; Schleinitz, Kathleen M; Vogt, Carsten

2012-05-01

Biodegradation of anthropogenic pollutants in shallow aquifers is an important microbial ecosystem service which is mainly brought about by indigenous anaerobic microorganisms. For the management of contaminated sites, risk assessment and control of natural attenuation, the assessment of in situ biodegradation and the underlying microbial processes is essential. The development of novel molecular methods, "omics" approaches, and high-throughput techniques has revealed new insight into complex microbial communities and their functions in anoxic environmental systems. This review summarizes recent advances in the application of molecular methods to study anaerobic microbial communities in contaminated terrestrial subsurface ecosystems. We focus on current approaches to analyze composition, dynamics, and functional diversity of subsurface communities, to link identity to activity and metabolic function, and to identify the ecophysiological role of not yet cultured microbes and syntrophic consortia. We discuss recent molecular surveys of contaminated sites from an ecological viewpoint regarding degrader ecotypes, abiotic factors shaping anaerobic communities, and biotic interactions underpinning the importance of microbial cooperation for microbial ecosystem services such as contaminant degradation.

Evaluation of the fate of arsenic-contaminated groundwater at different aquifers of Thar coalfield Pakistan.

Science.gov (United States)

Ali, Jamshed; Kazi, Tasneem G; Baig, Jameel A; Afridi, Hassan I; Arain, Mariam S; Ullah, Naeem; Brahman, Kapil D; Arain, Sadaf S; Panhwar, Abdul H

2015-12-01

In present study, the ground water at different aquifers was evaluated for physicochemical parameters, iron, total arsenic, total inorganic arsenic and arsenic species (arsenite and arsenate). The samples of groundwater were collected at different depths, first aquifer (AQ1) 50-60 m, second aquifer (AQ2) 100-120 m, and third aquifer (AQ3) 200-250 m of Thar coalfield, Pakistan. Total inorganic arsenic was determined by solid phase extraction using titanium dioxide as an adsorbent. The arsenite was determined by cloud point extraction using ammonium pyrrolidinedithiocarbamate as a chelating reagent, and resulted complex was extracted by Triton X-114. The resulted data of groundwater were reported in terms of basic statistical parameters, principal component, and cluster analysis. The resulted data indicated that physicochemical parameters of groundwater of different aquifers were exceeded the World Health Organization provisional guideline for drinking water except pH and SO4(2-). The positive correlation was observed between arsenic species and physicochemical parameters of groundwater except F(-) and K(+), which might be caused by geochemical minerals. Results of cluster analysis indicated that groundwater samples of AQ1 was highly contaminated with arsenic species as compared to AQ2 and AQ3 (p > 0.05).

Assessments of aquifer sensitivity on Navajo Nation and adjacent lands and ground-water vulnerability to pesticide contamination on the Navajo Indian Irrigation Project, Arizona, New Mexico, and Utah

Science.gov (United States)

Blanchard, Paul J.

2002-01-01

The U.S. Environmental Protection Agency requested that the Navajo Nation conduct an assessment of aquifer sensitivity on Navajo Nation lands and an assessment of ground-water vulnerability to pesticide contamination on the Navajo Indian Irrigation Project. Navajo Nation lands include about 17,000 square miles in northeastern Arizona, northwestern New Mexico, and southeastern Utah. The Navajo Indian Irrigation Project in northwestern New Mexico is the largest area of agriculture on the Navajo Nation. The Navajo Indian Irrigation Project began operation in 1976; presently (2001) about 62,000 acres are available for irrigated agriculture. Numerous pesticides have been used on the Navajo Indian Irrigation Project during its operation. Aquifer sensitivity is defined by the U.S. Environmental Protection Agency as 'The relative ease with which a contaminant [pesticide] applied on or near a land surface can migrate to the aquifer of interest. Aquifer sensitivity is a function of the intrinsic characteristics of the geologic material in question, any underlying saturated materials, and the overlying unsaturated zone. Sensitivity is not dependent on agronomic practices or pesticide characteristics.' Ground-water vulnerability is defined by the U.S. Environmental Protection Agency as 'The relative ease with which a contaminant [pesticide] applied on or near a land surface can migrate to the aquifer of interest under a given set of agronomic management practices, pesticide characteristics, and aquifer sensitivity conditions.' The results of the aquifer sensitivity assessment on Navajo Nation and adjacent lands indicated relative sensitivity within the boundaries of the study area. About 22 percent of the study area was not an area of recharge to bedrock aquifers or an area of unconsolidated deposits and was thus assessed to have an insignificant potential for contamination. About 72 percent of the Navajo Nation study area was assessed to be in the categories of most potential

The Effects of Surfactants on the Desorption of Organic Contaminants from Aquifer Materials

Science.gov (United States)

1989-08-01

costs for remediating a contaminated aquifer can be reduced by 50-80 percent using this system. A preflush of 0.1-1.0 percent concentration potassium ...use of polymers such as polyacrylic acid and polyacrylamide as sacrificial adsorbates to decrease the adsorption of a mixed nonionic and anionic...cribed by Chapman (1965) in Methods of Soils Analysis was used to determine the masses of extractable sodium, potassium , calcium and mag- nesium

contaminant migration in a sand aquifer near an inactive uranium tailings impoundment, Elliot Lake, Ontario

International Nuclear Information System (INIS)

Morin, K.A.; Cherry, J.A.

1982-01-01

An investigation of the movement of contaminated groundwater from inactive uranium tailings through a sand aquifer is being conducted at the Nordic Main tailings impoundment near Elliot Lake, Ontario. During 1979 and 1980, multilevel bundle-type piezometers were installed at several locations around the edge of the tailings impoundment. Chemical analysis of water samples from the bundle piezometers indicate that a major contaminant plume extends outward through a sand aquifer from the southeastern part of the Nordic Main impoundment dam. In the vincinity of the contaminant plume, the sand aquifer varies in thickness from about 9 to 15 m. The plume has two distinct segments, referred to as the inner core and the outer zone. The inner core, which has a pH of 4.3-5.0 and extends about 15 m from the foot of the tailings dam, contains several grams per litre of iron and sulfate, and tens of pCi/L of 226 Ra and 210 Pb. Water levels in piezometers within the inner core show that groundwater is moving horizontally, away from the tailings impoundment, with a velocity of up to several hundred metres per year. The outer zone, which extends a few hundred metres downgradient from the dam, is characterized by hundreds to thousands of milligrams per litre of iron and sulfate, less than 15pCi/L of 226 Ra, and a pH greater than 5.7. Comparison of 1979 and 1980 data shows that the front of the inner core is advancing a few metres per year, which is less than a few percent of the groundwater velocity. This retardation of movement of the inner core is caused by neutralization of the acidic water as a result of dissolution of calcium carbonate in the sand. With the rise in pH, precipitation of iron carbonate and possibly some iron hydroxide occurs and the contaminants of main concern such as 226 Ra, 210 Pb, and uranium are removed from solution by adsorption or coprecipitation

Contamination risk and drinking water protection for a large-scale managed aquifer recharge site in a semi-arid karst region, Jordan

Science.gov (United States)

Xanke, Julian; Liesch, Tanja; Goeppert, Nadine; Klinger, Jochen; Gassen, Niklas; Goldscheider, Nico

2017-09-01

Karst aquifers in semi-arid regions are particularly threatened by surface contamination, especially during winter seasons when extremely variable rainfall of high intensities prevails. An additional challenge is posed when managed recharge of storm water is applied, since karst aquifers display a high spatial variability of hydraulic properties. In these cases, adapted protection concepts are required to address the interaction of surface water and groundwater. In this study a combined protection approach for the surface catchment of the managed aquifer recharge site at the Wala reservoir in Jordan and the downstream Hidan wellfield, which are both subject to frequent bacteriological contamination, is developed. The variability of groundwater quality was evaluated by correlating contamination events to rainfall, and to recharge from the reservoir. Both trigger increased wadi flow downstream of the reservoir by surface runoff generation and groundwater seepage, respectively. A tracer test verified the major pathway of the surface flow into the underground by infiltrating from pools along Wadi Wala. An intrinsic karst vulnerability and risk map was adapted to the regional characteristics and developed to account for the catchment separation by the Wala Dam and the interaction of surface water and groundwater. Implementation of the proposed protection zones for the wellfield and the reservoir is highly recommended, since the results suggest an extreme contamination risk resulting from livestock farming, arable agriculture and human occupation along the wadi. The applied methods can be transferred to other managed aquifer recharge sites in similar karstic environments of semi-arid regions.

Field demonstration of foam injection to confine a chlorinated solvent source zone.

Science.gov (United States)

Portois, Clément; Essouayed, Elyess; Annable, Michael D; Guiserix, Nathalie; Joubert, Antoine; Atteia, Olivier

2018-05-01

A novel approach using foam to manage hazardous waste was successfully demonstrated under active site conditions. The purpose of the foam was to divert groundwater flow, that would normally enter the source zone area, to reduce dissolved contaminant release to the aquifer. During the demonstration, foam was pre generated and directly injected surrounding the chlorinated solvent source zone. Despite the constraints related to the industrial activities and non-optimal position of the injection points, the applicability and effectiveness of the approach have been highlighted using multiple metrics. A combination of measurements and modelling allowed definition of the foam extent surrounding each injection point, and this appears to be the critical metric to define the success of the foam injection approach. Information on the transport of chlorinated solvents in groundwater showed a decrease of contaminant flux by a factor of 4.4 downstream of the confined area. The effective permeability reduction was maintained over a period of three months. The successful containment provides evidence for consideration of the use of foam to improve traditional flushing techniques, by increasing the targeting of contaminants by remedial agents. Copyright © 2018 Elsevier B.V. All rights reserved.

Field Investigation of Natural Attenuation of a Petroleum Hydrocarbon Contaminated Aquifer, Gyeonggi Province, Korea

Science.gov (United States)

Yang, J.; Lee, K.; Bae, G.

2004-12-01

In remediation of a petroleum hydrocarbon contaminated aquifer, natural attenuation may be significant as a remedial alternative. Therefore, natural attenuation should be investigated in the field in order to effectively design and evaluate the remediation strategy at the contaminated site. This study focused on evaluating the natural attenuation for benzene, toluene, ethylbenzene, and xylene (BTEX) at a contaminated site in South Korea. At the study site, the aquifer is composed of a high permeable gravel layer and relatively low permeable sandy-silt layers. Groundwater level vertically fluctuated between 1m and 2m throughout the year (April, 2003~June, 2004) and showed direct response to rainfall events. Chemical analyses of sampled groundwater were performed to investigate the concentrations of various chemical species which are associated with the natural attenuation processes. To evaluate the degree of the biodegradation, the expressed biodegradation capacity (EBC) analysis was done using aerobic respiration, nitrate reduction, manganese reduction, ferric iron reduction, and sulfate reduction as an indicator. High EBC value of sulfate indicate that anaerobic biodegradation by sulfate reduction was a dominant process of mineralization of BTEX at this site. The EBC values decrease sensitively when heavy rainfall occurs due to the dilution and inflow of electron acceptors through a gravel layer. The first-order biodegradation rates of BTEX were estimated by means of the Buscheck and Alcantar method (1995). Results show that the natural attenuation rate of benzene was the highest among the BTEX.

Factors affecting public-supply well vulnerability in two karst aquifers.

Science.gov (United States)

Musgrove, MaryLynn; Katz, Brian G; Fahlquist, Lynne S; Crandall, Christy A; Lindgren, Richard J

2014-09-01

Karst aquifers occur in a range of climatic and geologic settings. Nonetheless, they are commonly characterized by their vulnerability to water-quality impairment. Two karst aquifers, the Edwards aquifer in south-central Texas and the Upper Floridan aquifer in western Florida, were investigated to assess factors that control the movement of contaminants to public-supply wells (PSWs). The geochemistry of samples from a selected PSW or wellfield in each aquifer was compared with that from nearby monitoring wells and regional PSWs. Geochemistry results were integrated with age tracers, flow modeling, and depth-dependent data to refine aquifer conceptual models and to identify factors that affect contaminant movement to PSWs. The oxic Edwards aquifer is vertically well mixed at the selected PSW/wellfield, although regionally the aquifer is geochemically variable downdip. The mostly anoxic Upper Floridan aquifer is affected by denitrification and also is geochemically variable with depth. In spite of considerable differences in geology and hydrogeology, the two aquifers are similarly vulnerable to anthropogenic contamination. Vulnerability in studied PSWs in both aquifers is strongly influenced by rapid karst flowpaths and the dominance of young (aquifers (nitrate, atrazine, deethylatrazine, tetrachloroethene, and chloroform). Specific consideration of water-quality protection efforts, well construction and placement, and aquifer response times to land-use changes and contaminant loading are discussed, with implications for karst groundwater management. © 2014 The Authors. Groundwater published by Wiley Periodicals, Inc. on behalf of National Ground Water Association.

Effect of nitrate addition on biorestoration of fuel-contaminated aquifer: Field demonstration

International Nuclear Information System (INIS)

Hutchins, S.R.; Downs, W.C.; Wilson, J.T.; Smith, G.B.; Kovacs, D.A.

1991-01-01

A spill of JP-4 jet fuel at the U.S. Coast Guard Air Station in Traverse City, Michigan, contaminated a water-table aquifer. An infiltration gallery (30 ft X 30 ft) was installed above a section of the aquifer containing 700 gal JP-4. Purge wells recirculated three million gallons of ground water per week through the infiltration gallery at a rate designed to raise the water table above the contaminated interval. Ground water containing ambient concentrations was first recirculated for 40 days. Concentrations of benzene in monitoring wells beneath the infiltration gallery were reduced from 760 to <1 micrograms/1. Concentrations of toluene, ethylbenzene, m,p-xylene, and o-xylene were reduced from 4500 to 17,840 to 44,2600 to 490, and 1400 to 260 micrograms/1, respectively. Average core concentrations of benzene, toluene, ethylbenzene, m,p-xylene, and o-xylene were reduced from 0.84 to 0.032, 33 to 0.13, 18 to 0.36, 58 to 7.4, and 26 to 3.2 mg/kg, respectively. Ground water amended with nitrate (10 mg/1 nitrate-nitrogen) and nutrients was then recirculated for 76 days. Final core concentrations of benzene, toluene, ethylbenzene, m,p-xylene and o-xylene were 0.017, 0.036, 0.019, 0.059, and 0.27 mg/kg, respectively. Final aqueous concentrations were <1 micrograms/1 for benzene and toluene, 6 micrograms/1 for ethylbenzene, and 20 to 40 micrograms/1 for the xylene isomers, in good agreement with predicted values based on residual fuel content and partitioning theory. Although alkylbenzene concentrations have been substantially reduced, the test plot is still contaminated with the weathered fuel. Based on stoichiometry, approximately 10 times more nitrate was consumed than could be accounted for by BTX degradation alone, indicating that other compounds were also degraded under denitrifying conditions

Microbial community composition during anaerobic mineralization of tert-butyl alcohol (TBA) in fuel-contaminated aquifer material.

Science.gov (United States)

Wei, Na; Finneran, Kevin T

2011-04-01

Anaerobic mineralization of tert-butyl alcohol (TBA) and methyl tert-butyl ether (MTBE) were studied in sediment incubations prepared with fuel-contaminated aquifer material. Microbial community compositions in all incubations were characterized by amplified ribosomal DNA restriction analysis (ARDRA). The aquifer material mineralized 42.3±9.9% of [U-(14)C]-TBA to 14CO2 without electron acceptor amendment. Fe(III), sulfate, and Fe(III) plus anthraquinone-2,6-disulfonate addition also promoted U-[14C]-TBA mineralization at levels similar to those of the unamended controls. Nitrate actually inhibited TBA mineralization relative to unamended controls. In contrast to TBA, [U-(14)C]-MTBE was not significantly mineralized in 400 days regardless of electron acceptor amendment. Microbial community analysis indicated that the abundance of one dominant clone group correlated closely with anaerobic TBA mineralization. The clone was phylogenetically distinct from known aerobic TBA-degrading microorganisms, Fe(III)- or sulfate-reducing bacteria. It was most closely associated with organisms belonging to the alphaproteobacteria. Microbial communities were different in MTBE and TBA amended incubations. Shannon indices and Simpson indices (statistical community comparison tools) both demonstrated that microbial community diversity decreased in incubations actively mineralizing TBA, with distinct "dominant" clones developing. These data contribute to our understanding of anaerobic microbial transformation of fuel oxygenates in contaminated aquifer material and the organisms that may catalyze the reactions.

Denitrification and dilution along fracture flowpaths influence the recovery of a bedrock aquifer from nitrate contamination

Energy Technology Data Exchange (ETDEWEB)

Kim, Jonathan J., E-mail: jon.kim@vermont.gov [Vermont Geological Survey, 1 National Life Drive, Main 2, Montpelier, VT 05620 (United States); Comstock, Jeff [Vermont Agency of Agriculture, 116 State Street, Montpelier, VT 05620 (United States); Ryan, Peter [Dept. of Geology, Middlebury College, Middlebury, VT 05753 (United States); Heindel, Craig [Waite-Heindel Environmental Management, 7 Kilburn Street, Suite 301, Burlington, VT 05401 (United States); Koenigsberger, Stephan [Dept. of Geology, Middlebury College, Middlebury, VT 05753 (United States)

2016-11-01

In 2000, elevated nitrate concentrations ranging from 12 to 34 mg/L NO{sub 3}−N were discovered in groundwater from numerous domestic bedrock wells adjacent to a large dairy farm in central Vermont. Long-term plots and contours of nitrate vs. time for bedrock wells showed “little/no”, “moderate”, and “large” change patterns that were spatially separable. The metasedimentary bedrock aquifer is strongly anisotropic and groundwater flow is controlled by fractures, bedding/foliation, and basins and ridges in the bedrock surface. Integration of the nitrate concentration vs. time data and the physical and chemical aquifer characterization suggest two nitrate sources: a point source emanating from a waste ravine and a non-point source that encompasses the surrounding fields. Once removed, the point source of NO{sub 3} (manure deposited in a ravine) was exhausted and NO{sub 3} dropped from 34 mg/L to < 10 mg/L after ~ 10 years; however, persistence of NO{sub 3} in the 3 to 8 mg/L range (background) reflects the long term flux of nitrates from nutrients applied to the farm fields surrounding the ravine over the years predating and including this study. Inferred groundwater flow rates from the waste ravine to either moderate change wells in basin 2 or to the shallow bedrock zone beneath the large change wells are 0.05 m/day, well within published bedrock aquifer flow rates. Enrichment of {sup 15}N and {sup 18}O in nitrate is consistent with lithotrophic denitrification of NO{sub 3} in the presence of dissolved Mn and Fe. Once the ravine point-source was removed, denitrification and dilution collectively were responsible for the down-gradient decrease of nitrate in this bedrock aquifer. Denitrification was most influential when NO{sub 3}−N was > 10 mg/L. Our multidisciplinary methods of aquifer characterization are applicable to groundwater contamination in any complexly-deformed and metamorphosed bedrock aquifer. - Highlights: • Bedrock wells contaminated

The dispersal of contaminants in heterogeneous aquifers: a review of methods of estimating scale dependent parameters

International Nuclear Information System (INIS)

Farmer, C.L.

1986-02-01

The design and assessment of underground waste disposal options requires modelling the dispersal of contaminants within aquifers. The logical structure of the development and application of disposal models is discussed. In particular we examine the validity and interpretation of the gradient diffusion model. The effective dispersion parameters in such a model seem to depend upon the scale on which they are measured. This phenomenon is analysed and methods for modelling scale dependent parameters are reviewed. Specific recommendations regarding the modelling of contaminant dispersal are provided. (author)

Chemical and microbiological monitoring of a sole-source aquifer intended for artificial recharge, Nassau County, New York

Science.gov (United States)

Katz, Brian G.; Mallard, Gail E.

1980-01-01

In late 1980, approximately 4 million gallons per day of highly treated wastewater will be used to recharge the groundwater reservoir in central Nassau County through a system of 10 recharge basins and 5 shallow injection wells. To evaluate the impact of large-scale recharge with reclaimed water on groundwater quality, the U.S. Geological Survey has collected hydrologic and water-quality data from a 1-square-mile area around the recharge site to provide a basis for future comparison. Extensive chemical and microbiological analyses are being made on samples from 48 wells screened in the upper glacial (water-table) aquifer and the upper part of the underlying Magothy (public-supply) aquifer. Preliminary results indicate that water from the upper glacial aquifer contains significant concentrations of nitrate and low-molecular-weight chlorinated hydrocarbons and detectable concentrations of organochlorine insecticides and polychlorinated biphenyls. At present, no fecal contamination is evident in either aquifer in the area studied. In the few samples containing fecal indicator bacteria, the numbers were low. Nonpoint sources provide significant loads of organic and inorganic compounds; major sources include cesspool and septic-tank effluent, cesspool and septic-tank cleaners and other over-the-counter domestic organic solvents, fertilizers, insecticides for termite and other pest control, and stormwater runoff to recharge basins. The water-table aquifer is composed mainly of stratified, well-sorted sand and gravel and, as a result, is highly permeable. In the 1-square-mile area studied, some contaminants seem to have traveled 200 feet downward to the bottom of the water-table aquifer and into the upper part of the public-supply aquifer. (USGS)

Radionuclides, Heavy Metals and Fluoride Contamination in Al Bahira Aquifer, Youssoufia Area, Morocco

Energy Technology Data Exchange (ETDEWEB)

Agma, T. T; Bouchaou, L.; Ettayfi, N.; Lgourna, Z.; Boutaleb, S. [Ibn Zohr University, Applied Geology and Geo-Environment Laboratory, Cite Dakhla, Agadir 80060 (Morocco); Warner, N.; Vengosh, A. [Duke University, Division of Earth and Ocean Sciences, Durham, NC 27708 (United States)

2013-07-15

This study investigates the geochemistry and quantity of trace metals and naturally occurring radionuclides (Ra, U) in the shallow groundwater in the western part of the Al Bahira aquifer (Phosphate Plateau) located in west central Morocco. Groundwater is characterized by a wide salinity range (TDS of 540 to 9286 mg/l) and shows systematic linear relationships between the major dissolved constituents. These relationships suggest that the mixing of a single saline source and fresh water controls the quality of groundwater. Fluoride, uranium, selenium, and arsenic concentrations are also correlated with salinity. The activity concentrations of Radium-226 exceed the US-EPA drinking water standard. Radium-226 activity in the groundwater is not directly related to salinity and might be affected by other factors such as water temperature. The low ratios of the short lived Ra-224 to Ra-223 ({approx}2) indicate that Ra was derived from a uranium rich source with a low Th/U ratio in the rock source, which is consistent with the Urich lithology of the aquifer (e.g., phosphate rocks). The high levels of contaminants found in the shallow groundwater samples have important health implications for the local population, as shallow groundwater is used for drinking water in the rural communities northwest of Marrakech and these contaminants pose potential serious health problems (e.g., dental fluorosis, kidney disease, and bone cancer). (author)

Activated Persulfate Treatment of 1,4-Dioxane in the Presence of Chlorinated Solvent Co-contaminants

Science.gov (United States)

Boving, T. T.; Eberle, D. E. H.; Ball, R.

2014-12-01

1,4-dioxane is an emerging groundwater contaminant and a likely human carcinogen. Due to its history as a stabilizer in chlorinated solvents, 1,4-dioxane is often found as a co-contaminant at solvent releases sites such as landfills, solvent recycling facilities, vapor decreasing operations, and fire-training areas. Historically, 1,4-dioxane was not routinely analyzed for at solvent release sites. The lack of analyses and the limitations of the analyses that were performed (i.e. high reporting limits) means that the scale of 1,4-dioxane subsurface contamination is still emerging. With the number of known 1,4-dioxane sites increasing, the need for cost effective 1,4-dioxane remediation technologies is rising as well. Remediation strategies that are capable of treating both 1,4-dioxane as well as chlorinated co-contaminants are of particular importance, especially when treating mixed-waste source zones. In the present study, we examined the fate of 1,4-dioxane during the targeted remediation of aqueous phase volatile organic compounds (VOC) using an activated persulfate based ISCO method (OxyZone®). Bench scale laboratory experiments are used to evaluate the treatability of 1,4-dioxane both as a single compound and in the presence of trichloroethene (TCE) and 1,1,1-trichloroethane (1,1,1-TCA). Possible dependencies on oxidant concentration and reaction kinetics were studied. Preliminary results are promising and show that OxyZone® is persistent and long lived, with oxidation of 1,4-dioxane continuing more than 12 days after initial dosage, even at dilute oxidant concentrations. The oxidative destruction of 1,4-dioxane, TCE and 1,1,1-TCA in single compound batch systems followed pseudo first order reaction kinetics. The rate of oxidation for each contaminant increased linearly with increasing persulfate concentration over the range of oxidant concentrations tested. The rate of oxidative destruction, from most easily degraded to least was: TCE > 1,4-Dioxane > 1

Using slow-release permanganate candles to remove TCE from a low permeable aquifer at a former landfill.

Science.gov (United States)

Christenson, Mark D; Kambhu, Ann; Comfort, Steve D

2012-10-01

Past disposal of industrial solvents into unregulated landfills is a significant source of groundwater contamination. In 2009, we began investigating a former unregulated landfill with known trichloroethene (TCE) contamination. Our objective was to pinpoint the location of the plume and treat the TCE using in situ chemical oxidation (ISCO). We accomplished this by using electrical resistivity imaging (ERI) to survey the landfill and map the subsurface lithology. We then used the ERI survey maps to guide direct push groundwater sampling. A TCE plume (100-600 μg L(-1)) was identified in a low permeable silty-clay aquifer (K(h)=0.5 md(-1)) that was within 6m of ground surface. To treat the TCE, we manufactured slow-release potassium permanganate candles (SRPCs) that were 91.4 cm long and either 5. cm or 7.6 cm in dia. For comparison, we inserted equal masses of SRPCs (7.6-cm versus 5.1-cm dia) into the low permeable aquifer in staggered rows that intersected the TCE plume. The 5.1-cm dia candles were inserted using direct push rods while the 7.6-cm SRPCs were placed in 10 permanent wells. Pneumatic circulators that emitted small air bubbles were placed below the 7.6-cm SRPCs in the second year. Results 15 months after installation showed significant TCE reductions in the 7.6-cm candle treatment zone (67-85%) and between 10% and 66% decrease in wells impacted by the direct push candles. These results support using slow-release permanganate candles as a means of treating chlorinated solvents in low permeable aquifers. Copyright © 2012 Elsevier Ltd. All rights reserved.

Characterizing pharmaceutical, personal care product, and hormone contamination in a karst aquifer of southwestern Illinois, USA, using water quality and stream flow parameters.

Science.gov (United States)

Dodgen, L K; Kelly, W R; Panno, S V; Taylor, S J; Armstrong, D L; Wiles, K N; Zhang, Y; Zheng, W

2017-02-01

Karst aquifers are drinking water sources for 25% of the global population. However, the unique geology of karst areas facilitates rapid transfer of surficial chemicals to groundwater, potentially contaminating drinking water. Contamination of karst aquifers by nitrate, chloride, and bacteria have been previously observed, but little knowledge is available on the presence of contaminants of emerging concern (CECs), such as pharmaceuticals. Over a 17-month period, 58 water samples were collected from 13 sites in the Salem Plateau, a karst region in southwestern Illinois, United States. Water was analyzed for 12 pharmaceutical and personal care products (PPCPs), 7 natural and synthetic hormones, and 49 typical water quality parameters (e.g., nutrients and bacteria). Hormones were detected in only 23% of samples, with concentrations of 2.2-9.1ng/L. In contrast, PPCPs were quantified in 89% of groundwater samples. The two most commonly detected PPCPs were the antimicrobial triclocarban, in 81% of samples, and the cardiovascular drug gemfibrozil, in 57%. Analytical results were combined with data of local stream flow, weather, and land use to 1) characterize the extent of aquifer contamination by CECs, 2) cluster sites with similar PPCP contamination profiles, and 3) develop models to describe PPCP contamination. Median detection in karst groundwater was 3 PPCPs at a summed concentration of 4.6ng/L. Sites clustered into 3 subsets with unique contamination models. PPCP contamination in Cluster I sites was related to stream height, manganese, boron, and heterotrophic bacteria. Cluster II sites were characterized by groundwater temperature, specific conductivity, sodium, and calcium. Cluster III sites were characterized by dissolved oxygen and barium. Across all sites, no single or small set of water quality factors was significantly predictive of PPCP contamination, although gemfibrozil concentrations were strongly related to the sum of PPCPs in karst groundwater

Determining shallow aquifer vulnerability by the DRASTIC model ...

Indian Academy of Sciences (India)

Shallow aquifer vulnerability has been assessed using GIS-based DRASTIC model by incorporating the major geological and hydrogeological factors that affect and control the groundwater contamination in a granitic terrain. It provides a relative indication of aquifer vulnerability to the contamination. Further, it has been ...

Final Rule: 2013 Conditional Exclusions From Solid Waste and Hazardous Waste for Solvent-Contaminated Wipes

Science.gov (United States)

This is a regulation page for the final rule EPA issued on July 31, 2013 that modifies the hazardous waste management regulations for solvent-contaminated wipes under the Resource Conservation and Recovery Act (RCRA).

VULNERABILITY AND RISK OF CONTAMINATION KARSTIC AQUIFERS

Directory of Open Access Journals (Sweden)

Yameli Aguilar

2013-08-01

Full Text Available Karstic systems occupy nearly 20% of the surface of the earth and are inhabited by numerous human communities. Karstic aquifers are the most exposed to pollution from human activities. Pollution of karstic aquifers is a severe environmental problem worldwide.  In order to face the vulnerability of karstic aquifers to pollution, researchers have created a diversity of study approaches and models, each one having their own strengths and weaknesses depending on the discipline from which they were originated, thus requiring a thorough discussion within the required multidisciplinary character. The objective of this article was to analyze the theoretical and methodological approaches applied to the pollution of karstic aquifers. The European hydrogeological, land evaluation, hydropedological and a geographic approach were analyzed. The relevance of a geomorphological analysis as a cartographic basis for the analysis of vulnerability and risks were emphasized. From the analysis of models, approaches and methodologies discussed the following recommendation is made: to form an interdisciplinary work team, to elaborate a conceptual model according to the site and the working scale and to e, apply and validate the model.

EPA Region 1 Sole Source Aquifers

Science.gov (United States)

This coverage contains boundaries of EPA-approved sole source aquifers. Sole source aquifers are defined as an aquifer designated as the sole or principal source of drinking water for a given aquifer service area; that is, an aquifer which is needed to supply 50% or more of the drinking water for the area and for which there are no reasonable alternative sources should the aquifer become contaminated.The aquifers were defined by a EPA hydrogeologist. Aquifer boundaries were then drafted by EPA onto 1:24000 USGS quadrangles. For the coastal sole source aquifers the shoreline as it appeared on the quadrangle was used as a boundary. Delineated boundaries were then digitized into ARC/INFO.

Molecular Analysis of Microbial Community Structures in Pristine and Contaminated Aquifers: Field and Laboratory Microcosm Experiments

Science.gov (United States)

Shi, Y.; Zwolinski, M. D.; Schreiber, M. E.; Bahr, J. M.; Sewell, G. W.; Hickey, W. J.

1999-01-01

This study used phylogenetic probes in hybridization analysis to (i) determine in situ microbial community structures in regions of a shallow sand aquifer that were oxygen depleted and fuel contaminated (FC) or aerobic and noncontaminated (NC) and (ii) examine alterations in microbial community structures resulting from exposure to toluene and/or electron acceptor supplementation (nitrate). The latter objective was addressed by using the NC and FC aquifer materials for anaerobic microcosm studies in which phylogenetic probe analysis was complemented by microbial activity assays. Domain probe analysis of the aquifer samples showed that the communities were predominantly Bacteria; Eucarya and Archaea were not detectable. At the phylum and subclass levels, the FC and NC aquifer material had similar relative abundance distributions of 43 to 65% β- and γ-Proteobacteria (B+G), 31 to 35% α-Proteobacteria (ALF), 15 to 18% sulfate-reducing bacteria, and 5 to 10% high G+C gram positive bacteria. Compared to that of the NC region, the community structure of the FC material differed mainly in an increased abundance of B+G relative to that of ALF. The microcosm communities were like those of the field samples in that they were predominantly Bacteria (83 to 101%) and lacked detectable Archaea but differed in that a small fraction (2 to 8%) of Eucarya was detected regardless of the treatment applied. The latter result was hypothesized to reflect enrichment of anaerobic protozoa. Addition of nitrate and/or toluene stimulated microbial activity in the microcosms, but only supplementation of toluene alone significantly altered community structures. For the NC material, the dominant subclass shifted from B+G to ALF, while in the FC microcosms 55 to 65% of the Bacteria community was no longer identifiable by the phylum or subclass probes used. The latter result suggested that toluene exposure fostered the proliferation of phylotype(s) that were otherwise minor constituents of the

Fundamental Studies of the Removal of Contaminants from Ground and Waste Waters via Reduction by Zero-Valent Metals

International Nuclear Information System (INIS)

Yarmoff, Jory A.; Amrhein, Christopher

1999-01-01

Contaminated groundwater and surface waters are a problem throughout the United States and the world. In many instances, the types of contamination can be directly attributed to man's actions. For instance, the burial of chemical wastes, casual disposal of solvents in unlined pits, and the development of irrigated agriculture have all contributed to groundwater and surface water contamination. The kinds of contaminants include chlorinated solvents and toxic trace elements (including radioisotopes) that are soluble and mobile in soils and aquifers. Oxyanions of uranium, selenium, chromium, arsenic, technetium, and chlorine (as perchlorate) are frequently found as contaminants on many DOE sites. Uranium is a particularly widespread contaminant at most DOE sites including Oak Ridge, Rocky Flats, Hanford, Idaho (INEEL), and Fernald. The uranium contamination is associated with mining and milling of uranium ore (UMTRA sites), isotope separation and enrichment, and mixed waste and TRU waste burial. In addition, the careless disposal of halogenated solvents, such as carbon tetrachloride and trichloroethylene, has further contaminated many groundwaters at these sites. A potential remediation method for many of these oxyanions and chlorinated-solvents is to react the contaminated water with zero-valent iron. In this reaction, the iron serves as both an electron source and as a catalyst. Elemental iron is already being used on an experimental basis at many DOE sites. Both in situ reactive barriers and above-ground reactors are being developed for this purpose. However, the design and operation of these treatment systems requires a detailed process-level understanding of the interactions between the contaminants and the iron surfaces. We are performing fundamental investigations of the interactions of the relevant chlorinated solvents and trace element-containing compounds with single- and poly-crystalline Fe surfaces. The aim of this work is to develop th e fundamental

Preliminary survey of the vulnerability to the contamination of the aquifers of Morondava river catchments

International Nuclear Information System (INIS)

Randrianasolo, A.F.

2004-01-01

The objective of this work is to make a preliminary survey of the vulnerability to the contamination of the aquifers of Morondava river catchments. The methods used are the geological and hydrogeological surveys, the hydrochemistry and isotopic techniques. This survey allows us to have an overview of the chemical features of groundwaters, conditions of recharge, and especially to determine the potential and active zone of nitrate pollution. Two field works have been carried out within the frame of MAG/8/003 project. The first one is focused on groundwater sampling and surface water sampling, and the second one is based on the geological and hydrogeological surveys. The samples were sent for isotope ( 18 O, 2 H, 15 N, 87 Sr, 3 H) and chemical analysis to the I.A.E.A laboratories. The survey gave the following conclusions: the groundwaters are affected by evaporation before or during infiltration and saline intrusion. The region of Morondava is submitted to a regime of simple oceanic precipitation (excess in deuterium). The boreholes waters is of sodic-bicarbonate chemical type, whereas well waters belong to the calcic-bicarbonate. The superficial aquifers (subsurface water) trapped by the wells are more vulnerable than deep aquifers (homogeneous aquifers) trapped by boreholes. These hypotheses are proven by geological and hydrogeological investigations, by the groundwaters nitrate analyses results, and are confirmed by radioactive isotope. [fr

Groundwater vulnerability mapping of Qatar aquifers

Science.gov (United States)

Baalousha, Husam Musa

2016-12-01

Qatar is one of the most arid countries in the world with limited water resources. With little rainfall and no surface water, groundwater is the only natural source of fresh water in the country. Whilst the country relies mainly on desalination of seawater to secure water supply, groundwater has extensively been used for irrigation over the last three decades, which caused adverse environmental impact. Vulnerability assessment is a widely used tool for groundwater protection and land-use management. Aquifers in Qatar are carbonate with lots of fractures, depressions and cavities. Karst aquifers are generally more vulnerable to contamination than other aquifers as any anthropogenic-sourced contaminant, especially above a highly fractured zone, can infiltrate quickly into the aquifer and spread over a wide area. The vulnerability assessment method presented in this study is based on two approaches: DRASTIC and EPIK, within the framework of Geographical Information System (GIS). Results of this study show that DRASTIC vulnerability method suits Qatar hydrogeological settings more than EPIK. The produced vulnerability map using DRASTIC shows coastal and karst areas have the highest vulnerability class. The southern part of the country is located in the low vulnerability class due to occurrence of shale formation within aquifer media, which averts downward movement of contaminants.

Modelling contaminant transport in saturated aquifers

International Nuclear Information System (INIS)

Lakshminarayana, V.; Nayak, T.R.

1990-01-01

With the increase in population and industrialization the problem of pollution of groundwater has become critical. The present study deals with modelling of pollutant transport through saturated aquifers. Using this model it is possible to predict the concentration distribution, spatial as well as temporal, in the aquifer. The paper also deals with one of the methods of controlling the pollutant movement, namely by pumping wells. A simulation model is developed to determine the number, location and rate of pumping of a number of wells near the source of pollution so that the concentration is within acceptable limits at the point of interest. (Author) (18 refs., 14 figs., tab.)

Viral and bacterial contamination in a sedimentary aquifer in Uruguay: evaluation of coliforms as regional indicators of viral contamination.

Science.gov (United States)

Gamazo, Pablo; Colina, Rodney; Victoria, Matias; Alvareda, Elena; Burutatran, Luciana; Ramos, Julian; Olivera, María; Soler, Joan

2015-04-01

In many areas of Uruguay groundwater is the only source of water for human consumption and for industrial-agricultural economic activities. Traditionally considered as a safe source, groundwater is commonly used without any treatment. The Uruguayan law requires bacteriological (fecal) analysis for most water uses, but virological analyses are not mentioned in the legislation. In the Salto district, where groundwater is used for human consumption and for agricultural activities, bacterial contamination has been detected in several wells but no viruses analysis have been performed. The Republic University (UDELAR), with the support of the National Agency for Research and Innovation (ANII), is studying the incidence of virus and fecal bacteria in groundwater on an intensive agriculture area of the Salto district. An initial screening campaign of 44 wells was performed in which, besides total and fecal coliforms, rotavirus and adenovirus were detected. A subgroup of the screening wells (15) where selected for bimonthly sampling during a year. In accordance with literature results, single well data analysis shows that coliform and viral contamination can be considered as independent variables. However, when spatial data is integrated, coliform and viral contamination show linear correlation. In this work we present the survey results, we analyse the temporal incidence of variables like precipitation, temperature and chemical composition in well contamination and we discuss the value of coliforms as global indicator of viral contamination for the Salto aquifer.

Stabilization of Rocky Flats combustible residues contaminated with plutonium metal and organic solvents

International Nuclear Information System (INIS)

Bowen, S.M.; Cisneros, M.R.; Jacobson, L.L.; Schroeder, N.C.; Ames, R.L.

1998-01-01

This report describes tests on a proposed flowsheet designed to stabilize combustible residues that were generated at the Rocky Flats Environmental Technology Site (RFETS) during the machining of plutonium metal. Combustible residues are essentially laboratory trash contaminated with halogenated organic solvents and plutonium metal. The proposed flowsheet, designed by RFETS, follows a glovebox procedure that includes (1) the sorting and shredding of materials, (2) a low temperature thermal desorption of solvents from the combustible materials, (3) an oxidation of plutonium metal with steam, and (4) packaging of the stabilized residues. The role of Los Alamos National Laboratory (LANL) in this study was to determine parameters for the low temperature thermal desorption and steam oxidation steps. Thermal desorption of carbon tetrachloride (CCl 4 ) was examined using a heated air stream on a Rocky Flats combustible residue surrogate contaminated with CCl 4 . Three types of plutonium metal were oxidized with steam in a LANL glovebox to determine the effectiveness of this procedure for residue stabilization. The results from these LANL experiments are used to recommend parameters for the proposed RFETS stabilization flowsheet

Electrokinetic-enhanced bioaugmentation for remediation of chlorinated solvents contaminated clay

International Nuclear Information System (INIS)

Mao, Xuhui; Wang, James; Ciblak, Ali; Cox, Evan E.; Riis, Charlotte; Terkelsen, Mads; Gent, David B.; Alshawabkeh, Akram N.

2012-01-01

Highlights: ► Simultaneous delivery of electron donors and bacteria into low permeability clays. ► Bacteria injection, growth and consequent transformation of contaminants are viable. ► EK injection is more effective than advection-based injection for clay soil. ► Electroosmosis appears to be the driving mechanism for bacteria injection. ► Both EK transport and biodegradation contribute the removal of VOCs in clay. - Abstract: Successful bioremediation of contaminated soils is controlled by the ability to deliver bioremediation additives, such as bacteria and/or nutrients, to the contaminated zone. Because hydraulic advection is not practical for delivery in clays, electrokinetic (EK) injection is an alternative for efficient and uniform delivery of bioremediation additive into low-permeability soil and heterogeneous deposits. EK-enhanced bioaugmentation for remediation of clays contaminated with chlorinated solvents is evaluated. Dehalococcoides (Dhc) bacterial strain and lactate ions are uniformly injected in contaminated clay and complete dechlorination of chlorinated ethene is observed in laboratory experiments. The injected bacteria can survive, grow, and promote effective dechlorination under EK conditions and after EK application. The distribution of Dhc within the clay suggests that electrokinetic transport of Dhc is primarily driven by electroosmosis. In addition to biodegradation due to bioaugmentation of Dhc, an EK-driven transport of chlorinated ethenes is observed in the clay, which accelerates cleanup of chlorinated ethenes from the anode side. Compared with conventional advection-based delivery, EK injection is significantly more effective for establishing microbial reductive dechlorination capacity in low-permeability soils.

Assessing the Vulnerability of Public-Supply Wells to Contamination: Central Valley Aquifer System near Modesto, California

Science.gov (United States)

Jagucki, Martha L.; Jurgens, Bryant C.; Burow, Karen R.; Eberts, Sandra M.

2009-01-01

This fact sheet highlights findings from the vulnerability study of a public-supply well in Modesto, California. The well selected for study pumps on average about 1,600 gallons per minute from the Central Valley aquifer system during peak summer demand. Water samples were collected at the public-supply well and at monitoring wells installed in the Modesto vicinity. Samples from the public-supply wellhead contained the undesirable constituents uranium, nitrate, arsenic, volatile organic compounds (VOCs), and pesticides, although none were present at concentrations exceeding drinking-water standards. Of these contaminants, uranium and nitrate pose the most significant water-quality risk to the public-supply well because human activities have caused concentrations in groundwater to increase over time. Overall, study findings point to four primary factors that affect the movement and (or) fate of contaminants and the vulnerability of the public-supply well in Modesto: (1) groundwater age (how long ago water entered, or recharged, the aquifer); (2) irrigation and agricultural and municipal pumping that drives contaminants downward into the primary production zone of the aquifer; (3) short-circuiting of contaminated water down the public-supply well during the low-pumping season; and (4) natural geochemical conditions of the aquifer. A local-scale computer model of groundwater flow and transport to the public-supply well was constructed to simulate long-term nitrate and uranium concentrations reaching the well. With regard to nitrate, two conflicting processes influence concentrations in the area contributing recharge to the well: (1) Beneath land that is being farmed or has recently been farmed (within the last 10 to 20 years), downward-moving irrigation waters contain elevated nitrate concentrations; yet (2) the proportion of agricultural land has decreased and the proportion of urban land has increased since 1960. Urban land use is associated with low nitrate

Characterization of chlorinated solvent contamination in limestone using innovative FLUTe® technologies in combination with other methods in a line of evidence approach

DEFF Research Database (Denmark)

Broholm, Mette Martina; Janniche, Gry Sander; Mosthaf, Klaus

2016-01-01

Characterization of dense non-aqueous phase liquid (DNAPL) source zones in limestone aquifers/bedrock is essential to develop accurate site-specific conceptual models and perform risk assessment. Here innovative field methods were combined to improve determination of source zone architecture......, hydrogeology and contaminant distribution. The FACT™ is a new technology and it was applied and tested at a contaminated site with a limestone aquifer, together with a number of existing methods including wire-line coring with core subsampling, FLUTe® transmissivity profiling and multilevel water sampling...... groundwater sampling (under two flow conditions) and FACT™ sampling and analysis combined with FLUTe® transmissivity profiling and modeling were used to provide a line of evidence for the presence of DNAPL, dissolved and sorbed phase contamination in the limestone fractures and matrix. The combined methods...

Assessing the vulnerability of public-supply wells to contamination: Rio Grande aquifer system in Albuquerque, New Mexico

Science.gov (United States)

Jagucki, Martha L.; Bexfield, Laura M.; Heywood, Charles E.; Eberts, Sandra M.

2012-01-01

This fact sheet highlights findings from the vulnerability study of a public-supply well in Albuquerque, New Mexico (hereafter referred to as “the study well”). The study well produces about 3,000 gallons of water per minute from the Rio Grande aquifer system. Water samples were collected at the study well, at two other nearby public-supply wells, and at monitoring wells installed in or near the simulated zone of contribution to the study well. Untreated water samples from the study well contained arsenic at concentrations exceeding the Maximum Contaminant Level (MCL) of 10 micrograms per liter (µg/L) established by the U.S. Environmental Protection Agency for drinking water. Volatile organic compounds (VOCs) and nitrate also were detected, although at concentrations at least an order of magnitude less than established drinking-water standards, where such standards exist. Overall, study findings point to four primary influences on the movement and (or) fate of contaminants and the vulnerability of the public-supply well in Albuquerque: (1) groundwater age (how long ago water entered, or recharged, the aquifer), (2) groundwater development (introduction of manmade recharge and discharge sources), (3) natural geochemical conditions of the aquifer, and (4) seasonal pumping stresses. Concentrations of the isotope carbon-14 indicate that groundwater from most sampled wells in the local study area is predominantly water that entered, or recharged, the aquifer more than 6,000 years ago. However, the additional presence of the age tracer tritium in several groundwater samples at concentrations above 0.3 tritium units indicates that young (post-1950) recharge is reaching the aquifer across broad areas beneath Albuquerque. This young recharge is mixing with the thousands-of-years-old water, is migrating to depths as great as 245 feet below the water table, and is traveling to some (but not all) of the public-supply wells sampled. Most groundwater samples containing a

Phytoremediation potential of willow tress for aquifers contaminated with ethanol-blended gasoline

Energy Technology Data Exchange (ETDEWEB)

Corseuil, H.X. [Universidade Federal de Santa Catarina, Florianopolis (Brazil). Departamento de Engenharia Sanitaria e Ambiental; Moreno, F.N. [Universidade do Sul de Santa Catarina, Palhoca (Brazil). Centro de Ciencias Agrarias e das Engenharias

2001-07-01

Ethanol-blended gasoline has been used in Brazil for 20 years and, probably, is going to be more widely used in North America due to the MtBE environmental effects on groundwater. The potential impacts caused by the presence of ethanol in UST spills are related to the co-solvency effect and the preferential degradation of ethanol over the BTEX compounds. These interactions may increase the length of dissolved hydrocarbon plumes and the costs associated with site remediation. This study investigates the advantages of phytoremediation to overcome the problems associated with the presence of ethanol in groundwater contaminated with gasoline-ethanol mixtures. Experiments were performed under lab conditions with cuttings of Willow tree (Salix babylonica) cultivated hydroponically. Results showed that the cuttings were able to reduce ethanol and benzene concentrations by more than 99% in less than a week. The uptake of both contaminants was confirmed by blank controls and was significantly related to cuttings transpiration capacity. Sorption onto roots biomass also markedly affected the behavior of contaminants in solution. Experiments to evaluate plants' toxicity to ethanol indicated that plants were only affected when aqueous ethanol concentration reached 2000mgl{sup -1}. Results suggest that phytoremediation can be a good complement to intrinsic remediation in shallow aquifer sites contaminated with ethanol-blended gasoline spills. (Author)

Vulnerability of a public supply well in a karstic aquifer to contamination.

Science.gov (United States)

Katz, B G; McBride, W S; Hunt, A G; Crandall, C A; Metz, P A; Eberts, S M; Berndt, M P

2009-01-01

To assess the vulnerability of ground water to contamination in the karstic Upper Floridan aquifer (UFA), age-dating tracers and selected anthropogenic and naturally occurring compounds were analyzed in multiple water samples from a public supply well (PSW) near Tampa, Florida. Samples also were collected from 28 monitoring wells in the UFA and the overlying surficial aquifer system (SAS) and intermediate confining unit located within the contributing recharge area to the PSW. Age tracer and geochemical data from the earlier stage of the study (2003 through 2005) were combined with new data (2006) on concentrations of sulfur hexafluoride (SF(6)), tritium ((3)H), and helium-3, which were consistent with binary mixtures of water for the PSW dominated by young water (less than 7 years). Water samples from the SAS also indicated mostly young water (less than 7 years); however, most water samples from monitoring wells in the UFA had lower SF(6) and (3)H concentrations than the PSW and SAS, indicating mixtures containing high proportions of older water (more than 60 years). Vulnerability of the PSW to contamination was indicated by predominantly young water and elevated nitrate-N and volatile organic compound concentrations that were similar to those in the SAS. Elevated arsenic (As) concentrations (3 to 19 microg/L) and higher As(V)/As(III) ratios in the PSW than in water from UFA monitoring wells indicate that oxic water from the SAS likely mobilizes As from pyrite in the UFA matrix. Young water found in the PSW also was present in UFA monitoring wells that tap a highly transmissive zone (43- to 53-m depth) in the UFA.

Metagenome-based metabolic reconstruction reveals the ecophysiological function of Epsilonproteobacteria in a hydrocarbon-contaminated sulfidic aquifer

Directory of Open Access Journals (Sweden)

Andreas Hardy Keller

2015-12-01

Full Text Available The population genome of an uncultured bacterium assigned to the Campylobacterales (Epsilonproteobacteria was reconstructed from a metagenome dataset obtained by whole-genome shotgun pyrosequencing. Genomic DNA was extracted from a sulfate-reducing, m-xylene-mineralizing enrichment culture isolated from groundwater of a benzene-contaminated sulfidic aquifer. The identical epsilonproteobacterial phylotype has previously been detected in toluene- or benzene-mineralizing, sulfate-reducing consortia enriched from the same site. Previous stable isotope probing experiments with 13C6-labeled benzene suggested that this phylotype assimilates benzene-derived carbon in a syntrophic benzene-mineralizing consortium that uses sulfate as terminal electron acceptor. However, the type of energy metabolism and the ecophysiological function of this epsilonproteobacterium within aromatic hydrocarbon-degrading consortia and in the sulfidic aquifer are poorly understood.Annotation of the epsilonproteobacterial population genome suggests that the bacterium plays a key role in sulfur cycling as indicated by the presence of a sqr gene encoding a sulfide quinone oxidoreductase and psr genes encoding a polysulfide reductase. It may gain energy by using sulfide or hydrogen/formate as electron donors. Polysulfide, fumarate, as well as oxygen are potential electron acceptors. Auto- or mixotrophic carbon metabolism seems plausible since a complete reductive citric acid cycle was detected. Thus the bacterium can thrive in pristine groundwater as well as in hydrocarbon-contaminated aquifers. In hydrocarbon-contaminated sulfidic habitats, the epsilonproteobacterium may generate energy by coupling the oxidation of hydrogen or formate and highly abundant sulfide with the reduction of fumarate and/or polysulfide, accompanied by efficient assimilation of acetate produced during fermentation or incomplete oxidation of hydrocarbons. The highly efficient assimilation of acetate was

Metagenome-Based Metabolic Reconstruction Reveals the Ecophysiological Function of Epsilonproteobacteria in a Hydrocarbon-Contaminated Sulfidic Aquifer.

Science.gov (United States)

Keller, Andreas H; Schleinitz, Kathleen M; Starke, Robert; Bertilsson, Stefan; Vogt, Carsten; Kleinsteuber, Sabine

2015-01-01

The population genome of an uncultured bacterium assigned to the Campylobacterales (Epsilonproteobacteria) was reconstructed from a metagenome dataset obtained by whole-genome shotgun pyrosequencing. Genomic DNA was extracted from a sulfate-reducing, m-xylene-mineralizing enrichment culture isolated from groundwater of a benzene-contaminated sulfidic aquifer. The identical epsilonproteobacterial phylotype has previously been detected in toluene- or benzene-mineralizing, sulfate-reducing consortia enriched from the same site. Previous stable isotope probing (SIP) experiments with (13)C6-labeled benzene suggested that this phylotype assimilates benzene-derived carbon in a syntrophic benzene-mineralizing consortium that uses sulfate as terminal electron acceptor. However, the type of energy metabolism and the ecophysiological function of this epsilonproteobacterium within aromatic hydrocarbon-degrading consortia and in the sulfidic aquifer are poorly understood. Annotation of the epsilonproteobacterial population genome suggests that the bacterium plays a key role in sulfur cycling as indicated by the presence of an sqr gene encoding a sulfide quinone oxidoreductase and psr genes encoding a polysulfide reductase. It may gain energy by using sulfide or hydrogen/formate as electron donors. Polysulfide, fumarate, as well as oxygen are potential electron acceptors. Auto- or mixotrophic carbon metabolism seems plausible since a complete reductive citric acid cycle was detected. Thus the bacterium can thrive in pristine groundwater as well as in hydrocarbon-contaminated aquifers. In hydrocarbon-contaminated sulfidic habitats, the epsilonproteobacterium may generate energy by coupling the oxidation of hydrogen or formate and highly abundant sulfide with the reduction of fumarate and/or polysulfide, accompanied by efficient assimilation of acetate produced during fermentation or incomplete oxidation of hydrocarbons. The highly efficient assimilation of acetate was recently

Impacts of physical and chemical aquifer heterogeneity on basin-scale solute transport: Vulnerability of deep groundwater to arsenic contamination in Bangladesh

Science.gov (United States)

Michael, Holly A.; Khan, Mahfuzur R.

2016-12-01

Aquifer heterogeneity presents a primary challenge in predicting the movement of solutes in groundwater systems. The problem is particularly difficult on very large scales, across which permeability, chemical properties, and pumping rates may vary by many orders of magnitude and data are often sparse. An example is the fluvio-deltaic aquifer system of Bangladesh, where naturally-occurring arsenic (As) exists over tens of thousands of square kilometers in shallow groundwater. Millions of people in As-affected regions rely on deep (≥150 m) groundwater as a safe source of drinking water. The sustainability of this resource has been evaluated with models using effective properties appropriate for a basin-scale contamination problem, but the extent to which preferential flow affects the timescale of downward migration of As-contaminated shallow groundwater is unknown. Here we embed detailed, heterogeneous representations of hydraulic conductivity (K), pumping rates, and sorptive properties (Kd) within a basin-scale numerical groundwater flow and solute transport model to evaluate their effects on vulnerability and deviations from simulations with homogeneous representations in two areas with different flow systems. Advective particle tracking shows that heterogeneity in K does not affect average travel times from shallow zones to 150 m depth, but the travel times of the fastest 10% of particles decreases by a factor of ∼2. Pumping distributions do not strongly affect travel times if irrigation remains shallow, but increases in the deep pumping rate substantially reduce travel times. Simulation of advective-dispersive transport with sorption shows that deep groundwater is protected from contamination over a sustainable timeframe (>1000 y) if the spatial distribution of Kd is uniform. However, if only low-K sediments sorb As, 30% of the aquifer is not protected. Results indicate that sustainable management strategies in the Bengal Basin should consider impacts of both

Assessing the mechanisms controlling the mobilization of arsenic in the arsenic contaminated shallow alluvial aquifer in the blackfoot disease endemic area

International Nuclear Information System (INIS)

Liao, Vivian Hsiu-Chuan; Chu, Yu-Ju; Su, Yu-Chen; Lin, Po-Cheng; Hwang, Yaw-Huei; Liu, Chen-Wuing; Liao, Chung-Min; Chang, Fi-John; Yu, Chan-Wei

2011-01-01

Highlights: ► Sedimentary microcosm showed simultaneous microbial reduction of Fe(III) and As(V). ► Addition of acetate caused a further increase in aqueous Fe(II) but not arsenic. ► An As(V)-reducing bacterium (ARS-3) native to aquifer sediments was isolated. ► ARS-3 showed microbial reduction of As(V) to As(III) in pore water in this aquifer. - Abstract: High levels of arsenic in groundwater and drinking water represent a major health problem worldwide. Drinking arsenic-contaminated groundwater is a likely cause of blackfoot disease (BFD) in Taiwan, but mechanisms controlling the mobilization of arsenic present at elevated concentrations within aquifers remain understudied. Microcosm experiments using sediments from arsenic contaminated shallow alluvial aquifers in the blackfoot disease endemic area showed simultaneous microbial reduction of Fe(III) and As(V). Significant soluble Fe(II) (0.23 ± 0.03 mM) in pore waters and mobilization of As(III) (206.7 ± 21.2 nM) occurred during the first week. Aqueous Fe(II) and As(III) respectively reached concentrations of 0.27 ± 0.01 mM and 571.4 ± 63.3 nM after 8 weeks. We also showed that the addition of acetate caused a further increase in aqueous Fe(II) but the dissolved arsenic did not increase. We further isolated an As(V)-reducing bacterium native to aquifer sediments which showed that the direct enzymatic reduction of As(V) to the potentially more-soluble As(III) in pore water is possible in this aquifer. Our results provide evidence that microorganisms can mediate the release of sedimentary arsenic to groundwater in this region and the capacity for arsenic release was not limited by the availability of electron donors in the sediments.

Assessing the mechanisms controlling the mobilization of arsenic in the arsenic contaminated shallow alluvial aquifer in the blackfoot disease endemic area

Energy Technology Data Exchange (ETDEWEB)

Liao, Vivian Hsiu-Chuan, E-mail: vivianliao@ntu.edu.tw [Department of Bioenvironmental Systems Engineering, National Taiwan University, 1 Roosevelt Road, Sec. 4, Taipei 106, Taiwan (China); Chu, Yu-Ju; Su, Yu-Chen; Lin, Po-Cheng [Department of Bioenvironmental Systems Engineering, National Taiwan University, 1 Roosevelt Road, Sec. 4, Taipei 106, Taiwan (China); Hwang, Yaw-Huei [Institute of Occupational Medicine and Industrial Hygiene, College of Public Health, National Taiwan University, 17 Xu-Zhou Road, Taipei 100, Taiwan (China); Liu, Chen-Wuing; Liao, Chung-Min; Chang, Fi-John; Yu, Chan-Wei [Department of Bioenvironmental Systems Engineering, National Taiwan University, 1 Roosevelt Road, Sec. 4, Taipei 106, Taiwan (China)

2011-12-15

Highlights: Black-Right-Pointing-Pointer Sedimentary microcosm showed simultaneous microbial reduction of Fe(III) and As(V). Black-Right-Pointing-Pointer Addition of acetate caused a further increase in aqueous Fe(II) but not arsenic. Black-Right-Pointing-Pointer An As(V)-reducing bacterium (ARS-3) native to aquifer sediments was isolated. Black-Right-Pointing-Pointer ARS-3 showed microbial reduction of As(V) to As(III) in pore water in this aquifer. - Abstract: High levels of arsenic in groundwater and drinking water represent a major health problem worldwide. Drinking arsenic-contaminated groundwater is a likely cause of blackfoot disease (BFD) in Taiwan, but mechanisms controlling the mobilization of arsenic present at elevated concentrations within aquifers remain understudied. Microcosm experiments using sediments from arsenic contaminated shallow alluvial aquifers in the blackfoot disease endemic area showed simultaneous microbial reduction of Fe(III) and As(V). Significant soluble Fe(II) (0.23 {+-} 0.03 mM) in pore waters and mobilization of As(III) (206.7 {+-} 21.2 nM) occurred during the first week. Aqueous Fe(II) and As(III) respectively reached concentrations of 0.27 {+-} 0.01 mM and 571.4 {+-} 63.3 nM after 8 weeks. We also showed that the addition of acetate caused a further increase in aqueous Fe(II) but the dissolved arsenic did not increase. We further isolated an As(V)-reducing bacterium native to aquifer sediments which showed that the direct enzymatic reduction of As(V) to the potentially more-soluble As(III) in pore water is possible in this aquifer. Our results provide evidence that microorganisms can mediate the release of sedimentary arsenic to groundwater in this region and the capacity for arsenic release was not limited by the availability of electron donors in the sediments.

Engineered and subsequent intrinsic in situ bioremediation of a diesel fuel contaminated aquifer

Science.gov (United States)

Hunkeler, Daniel; Höhener, Patrick; Zeyer, Josef

2002-12-01

A diesel fuel contaminated aquifer in Menziken, Switzerland was treated for 4.5 years by injecting aerated groundwater, supplemented with KNO 3 and NH 4H 2PO 4 to stimulate indigenous populations of petroleum hydrocarbon (PHC) degrading microorganisms. After dissolved PHC concentrations had stabilized at a low level, engineered in situ bioremediation was terminated. The main objective of this study was to evaluate the efficacy of intrinsic in situ bioremediation as a follow-up measure to remove PHC remaining in the aquifer after terminating engineered in situ bioremediation. In the first 7 months of intrinsic in situ bioremediation, redox conditions in the source area became more reducing as indicated by lower concentrations of SO 42- and higher concentrations of Fe(II) and CH 4. In the core of the source area, strongly reducing conditions prevailed during the remaining study period (3 years) and dissolved PHC concentrations were higher than during engineered in situ bioremediation. This suggests that biodegradation in the core zone was limited by the availability of oxidants. In lateral zones of the source area, however, gradually more oxidized conditions were reestablished again, suggesting that PHC availability increasingly limited biodegradation. The total DIC production rate in the aquifer decreased within 2 years to about 25% of that during engineered in situ bioremediation and remained at that level. Stable carbon isotope analysis confirmed that the produced DIC mainly originated from PHC mineralization. The total rate of DIC and CH 4 production in the source area was more than 300 times larger than the rate of PHC elution. This indicates that biodegradation coupled to consumption of naturally occurring oxidants was an important process for removal of PHC which remained in the aquifer after terminating engineered measures.

Intrinsic and enhanced bioremediation in aquifers contaminated with chlorinated and aromatic hydrocarbons in The Netherlands

NARCIS (Netherlands)

Rijnaarts, H.H.M.; Aalst-van Leeuwen, M.A. van; Heiningen, E. van; Buyzen, H. van; Sinke, A.; Liere, H.C. van; Harkes, M.; Baartmans, R.; Bosma, T.N.P.; Doddema, H.J.

1998-01-01

The feasibility of intrinsic and enhanced bioremediation approaches for 16 contaminated sites in the Netherlands are discussed. At at least five out of 10 chlorinated solvent sites, natural attenuation can be used as one of the tools to prevent further dispersion of the plume. At two sites

Probabilistic human health risk assessment of degradation-related chemical mixtures in heterogeneous aquifers: Risk statistics, hot spots, and preferential channels

Science.gov (United States)

Henri, Christopher V.; Fernàndez-Garcia, Daniel; de Barros, Felipe P. J.

2015-06-01

The increasing presence of toxic chemicals released in the subsurface has led to a rapid growth of social concerns and the need to develop and employ models that can predict the impact of groundwater contamination on human health risk under uncertainty. Monitored natural attenuation is a common remediation action in many contamination cases. However, natural attenuation can lead to the production of daughter species of distinct toxicity that may pose challenges in pollution management strategies. The actual threat that these contaminants pose to human health depends on the interplay between the complex structure of the geological media and the toxicity of each pollutant byproduct. This work addresses human health risk for chemical mixtures resulting from the sequential degradation of a contaminant (such as a chlorinated solvent) under uncertainty through high-resolution three-dimensional numerical simulations. We systematically investigate the interaction between aquifer heterogeneity, flow connectivity, contaminant injection model, and chemical toxicity in the probabilistic characterization of health risk. We illustrate how chemical-specific travel times control the regime of the expected risk and its corresponding uncertainties. Results indicate conditions where preferential flow paths can favor the reduction of the overall risk of the chemical mixture. The overall human risk response to aquifer connectivity is shown to be nontrivial for multispecies transport. This nontriviality is a result of the interaction between aquifer heterogeneity and chemical toxicity. To quantify the joint effect of connectivity and toxicity in health risk, we propose a toxicity-based Damköhler number. Furthermore, we provide a statistical characterization in terms of low-order moments and the probability density function of the individual and total risks.

The in-situ decontamination of sand and gravel aquifers by chemically enhanced solubilization of multiple-compound DNAPLs with surfactant solutions. Phase 1: Laboratory and pilot field-scale testing. Phase 2: Solubilization test and partitioning interwell tracer tests. Final report

International Nuclear Information System (INIS)

1997-01-01

Laboratory, numerical simulation, and field studies have been conducted to assess the potential use of micellar-surfactant solutions to solubilize chlorinated solvents contaminating sand and gravel aquifers. Ninety-nine surfactants were screened for their ability to solubilize trichloroethene (TCE), perchloroethylene (PCE), and carbon tetrachloride (CTET). The field test was conducted in the alluvial aquifer which is located 20 to 30 meters beneath a vapor degreasing operation at Paducah Gaseous Diffusion Plant. This aquifer has become contaminated with TCE due to leakage of perhaps 40,000 liters of TCE, which has generated a plume of dissolved TCE extending throughout an area of approximately 3 km 2 in the aquifer. Most of the TCE is believed to be present in the overlying lacustrine deposits and in the aquifer itself as a dense, non-aqueous phase liquid, or DNAPL. The objective of the field test was to assess the efficacy of the surfactant for in situ TCE solubilization. Although the test demonstrated that sorbitan monooleate was unsuitable as a solubilizer in this aquifer, the single-well test was demonstrated to be a viable method for the in situ testing of surfactants or cosolvents prior to proceeding to full-scale remediation

An evaluation of aquifer intercommunication between the unconfined and Rattlesnake Ridge aquifers on the Hanford Site

International Nuclear Information System (INIS)

Jensen, E.J.

1987-10-01

During 1986, Pacific Northwest Laboratory conducted a study of a portion of the Rattlesnake Ridge aquifer (confined aquifer) that lies beneath the B Pond - Gable Mountain Pond area of the Hanford Site. The purpose was to determine the extent of intercommunication between the unconfined aquifer and the uppermost regionally extensive confined aquifer, referred to as the Rattlesnake Ridge aquifer. Hydraulic head data and chemical data were collected from the ground water in the study area during December 1986. The hydraulic head data were used to determine the effects caused by water discharged to the ground from B Pond on both the water table of the unconfined aquifer and the potentiometric surface of the confined aquifer. The chemical data were collected to determine the extent of chemical constituents migrating from the unconfined aquifer to the confined aquifer. Analysis of chemical constituents in the Rattlesnake Ridge aquifer demonstrated that communication between the unconfined and confined aquifers had occurred. However, the levels of contaminants found in the Rattlesnake Ridge aquifer during this study were below the DOE Derived Concentration Guides

The in-situ decontamination of sand and gravel aquifers by chemically enhanced solubilization of multiple-compound DNAPLs with surfactant solutions: Phase 1 -- Laboratory and pilot field-scale testing and Phase 2 -- Solubilization test and partitioning and interwell tracer tests. Final report

Energy Technology Data Exchange (ETDEWEB)

NONE

1997-10-24

Laboratory, numerical simulation, and field studies have been conducted to assess the potential use of micellar-surfactant solutions to solubilize chlorinated solvents contaminating sand and gravel aquifers. Ninety-nine surfactants were screened for their ability to solubilize trichloroethene (TCE), perchloroethylene (PCE), and carbon tetrachloride (CTET). The field test was conducted in the alluvial aquifer which is located 20 to 30 meters beneath a vapor degreasing operation at Paducah Gaseous Diffusion Plant. This aquifer has become contaminated with TCE due to leakage of perhaps 40,000 liters of TCE, which has generated a plume of dissolved TCE extending throughout an area of approximately 3 km{sup 2} in the aquifer. Most of the TCE is believed to be present in the overlying lacustrine deposits and in the aquifer itself as a dense, non-aqueous phase liquid, or DNAPL. The objective of the field test was to assess the efficacy of the surfactant for in situ TCE solubilization. Although the test demonstrated that sorbitan monooleate was unsuitable as a solubilizer in this aquifer, the single-well test was demonstrated to be a viable method for the in situ testing of surfactants or cosolvents prior to proceeding to full-scale remediation.

Investigating the Sources of Nitrogen Contamination in the Shallow Aquifer of Jakarta using a Newly Developed Distributed River-Aquifer Flow and Transport Model

Science.gov (United States)

Costa, D.; Burlando, P.; Liong, S. Y.

2015-12-01

Recent observations in the shallow aquifer of Jakarta show a rise in nitrate (NO3-) levels. Groundwater is extensively used in the city to compensate for the limited public water supply network and therefore the risk to public health from a rise in NO3- concentration is high. NO3- has been identified as a cofactor for methemoglobinemia in infants, a disease which can lead to death in extreme cases. The NO3- levels detected are still below regulatory limits for drinking purposes but strategies are necessary to contain the growing problem. To this end, the main sources and pathways of inorganic compounds containing nitrogen (N) - i.e. nitrate, nitrite (NO2-) and ammonium (NH4+) - were investigated. We combined 3 years of field measurements in the Ciliwung River, the major river flowing through Jakarta, with a distributed river-aquifer interaction model to characterize the N-cycle in both systems and quantify the contribution of river infiltration in the overall groundwater N budget. The computed infiltration fluxes were compared to estimates of leaks from poorly maintained septic tanks, which are extensively used in the city, to identify the main source of groundwater contamination. Observations show a strong and interdependent spatial and seasonal variability in the levels of NO3-, NO2- and NH4+ in the river, which is caused by changes in nitrification/denitrification rates due to variations in dissolved oxygen concentrations. Simulation results suggest that such dynamics in the river cause river to aquifer contamination patterns to likewise change over space and time, which leads to heterogeneous vulnerability distributions. The estimated contribution of river-N infiltration to the observed NO3- groundwater levels is small if compared to that originating from all leaking septic tanks inside Jakarta. However, in the vicinity of the Ciliwung, river to groundwater N-loading can play an important role in the local NO3- groundwater levels because it is highly

Quaternary stratigraphy, sediment characteristics and geochemistry of arsenic-contaminated alluvial aquifers in the Ganges-Brahmaputra floodplain in central Bangladesh.

Science.gov (United States)

Shamsudduha, M; Uddin, A; Saunders, J A; Lee, M-K

2008-07-29

This study focuses on the Quaternary stratigraphy, sediment composition, mineralogy, and geochemistry of arsenic (As)-contaminated alluvial aquifers in the Ganges-Brahmaputra floodplain in the central Bangladesh. Arsenic concentrations in 85 tubewells in Manikganj area, 70 km northwest of Dhaka City, range from 0.25 microg/L to 191 microg/L with a mean concentration of 33 microg/L. Groundwater is mainly Ca-HCO(3) type with high concentrations of dissolved As, Fe, and Mn, but low level of SO(4). The uppermost aquifer occurs between 10 m and 80 m below the surface that has a mean arsenic concentration of 35 microg/L. Deeper aquifer (>100 m depth) has a mean arsenic concentration of 18 microg/L. Sediments in the upper aquifer are mostly gray to dark-gray, whereas sediments in the deep aquifer are mostly yellowing-gray to brown. Quartz, feldspar, mica, hornblende, garnet, kyanite, tourmaline, magnetite, ilmenite are the major minerals in sediments from both aquifers. Biotite and potassium feldspar are dominant in shallow aquifer, although plagioclase feldspar and garnet are abundant in deep aquifer sediments. Sediment composition suggests a mixed provenance with sediment supplies from both orogenic belts and cratons. High arsenic concentrations in sediments are found within the upper 50 m in drilled core samples. Statistical analysis shows that As, Fe, Mn, Ca, and P are strongly correlated in sediments. Concentrations of Cd, Cu, Ni, Zn, and Bi also show strong correlations with arsenic in the Manikganj sediment cores. Authigenic goethite concretions, possibly formed by bacteria, are found in the shallow sediments, which contain arsenic of a concentration as high as 8.8 mg/kg. High arsenic concentrations in aquifers are associated with fine-grained sediments that were derived mostly from the recycled orogens and relatively rapidly deposited mainly by meandering channels during the Early to Middle Holocene rising sea-level conditions.

Assessing the mechanisms controlling the mobilization of arsenic in the arsenic contaminated shallow alluvial aquifer in the blackfoot disease endemic area.

Science.gov (United States)

Liao, Vivian Hsiu-Chuan; Chu, Yu-Ju; Su, Yu-Chen; Lin, Po-Cheng; Hwang, Yaw-Huei; Liu, Chen-Wuing; Liao, Chung-Min; Chang, Fi-John; Yu, Chan-Wei

2011-12-15

High levels of arsenic in groundwater and drinking water represent a major health problem worldwide. Drinking arsenic-contaminated groundwater is a likely cause of blackfoot disease (BFD) in Taiwan, but mechanisms controlling the mobilization of arsenic present at elevated concentrations within aquifers remain understudied. Microcosm experiments using sediments from arsenic contaminated shallow alluvial aquifers in the blackfoot disease endemic area showed simultaneous microbial reduction of Fe(III) and As(V). Significant soluble Fe(II) (0.23±0.03 mM) in pore waters and mobilization of As(III) (206.7±21.2 nM) occurred during the first week. Aqueous Fe(II) and As(III) respectively reached concentrations of 0.27±0.01 mM and 571.4±63.3 nM after 8 weeks. We also showed that the addition of acetate caused a further increase in aqueous Fe(II) but the dissolved arsenic did not increase. We further isolated an As(V)-reducing bacterium native to aquifer sediments which showed that the direct enzymatic reduction of As(V) to the potentially more-soluble As(III) in pore water is possible in this aquifer. Our results provide evidence that microorganisms can mediate the release of sedimentary arsenic to groundwater in this region and the capacity for arsenic release was not limited by the availability of electron donors in the sediments. Copyright © 2011 Elsevier B.V. All rights reserved.

Ground-water flow in the surficial aquifer system and potential movement of contaminants from selected waste-disposal sites at Cecil Field Naval Air Station, Jacksonville, Florida

Science.gov (United States)

Halford, K.J.

1998-01-01

As part of the Installation Restoration Program, Cecil Field Naval Air Station, Jacksonville, Florida, is considering remedialaction alternatives to control the possible movement of contaminants from sites that may discharge to the surface. This requires a quantifiable understanding of ground-water flow through the surficial aquifer system and how the system will respond to any future stresses. The geologic units of interest in the study area consist of sediments of Holocene to Miocene age that extend from land surface to the base of the Hawthorn Group. The hydrogeology within the study area was determined from gamma-ray and geologists? logs. Ground-water flow through the surficial aquifer system was simulated with a seven-layer, finite-difference model that extended vertically from the water table to the top of the Upper Floridan aquifer. Results from the calibrated model were based on a long-term recharge rate of 6 inches per year, which fell in the range of 4 to 10 inches per year, estimated using stream hydrograph separation methods. More than 80 percent of ground-water flow circulates within the surficial-sand aquifer, which indicates that most contaminant movement also can be expected to move through the surficial-sand aquifer alone. The surficial-sand aquifer is the uppermost unit of the surficial aquifer system. Particle-tracking results showed that the distances of most flow paths were 1,500 feet or less from a given site to its discharge point. For an assumed effective porosity of 20 percent, typical traveltimes are 40 years or less. At all of the sites investigated, particles released 10 feet below the water table had shorter traveltimes than those released 40 feet below the water table. Traveltimes from contaminated sites to their point of discharge ranged from 2 to 300 years. The contributing areas of the domestic supply wells are not very extensive. The shortest traveltimes for particles to reach the domestic supply wells from their respective

Assessment of Intrinsic Vulnerability to Contamination for the Alluvial Aquifer in El-Fayoum Depression Using the Drastic Method

International Nuclear Information System (INIS)

Ahmed, M.A.

2012-01-01

Intrinsic vulnerability assessment to delineate areas that are more susceptible to contamination from anthropogenic sources has become an important element for sensible resource management and land use planning. The vulnerability for the alluvial aquifer in El-Fayoum depression was assessed by applying the Drastic model as well as utilizing sensitivity analyses to evaluate the reliability of this model. This method uses seven parameters including climatic, geological, and hydrogeological conditions controlling the seepage of pollutant substances to groundwater. Vulnerability maps were produced by applying the Generic and Agricultural models according to the Drastic charter. The resulting agricultural Drastic vulnerability map indicates that 23.3%, 22.7% and 12.4% of El-Fayoum depression is under low, low-moderate and moderately high vulnerability of groundwater contamination, respectively, while 41.6% of the area of study can be designated as an area of moderate vulnerability of groundwater contamination. Resulting maps revealed that the potential for polluting groundwater with agricultural chemicals is greater than with Generic Drastic index pollutants. Depth to water table parameter inflicted the largest impact on the intrinsic vulnerability of the alluvial aquifer in El-Fayoum depression. Both the map removal and single-parameter sensitivity analyses indicated that the vulnerability index is the least sensitive to the removal of the recharge and hydraulic conductivity parameters but is highly sensitive to the removal of depth to water parameter.

Engineered in situ bioremediation of a petroleum hydrocarbon-contaminated aquifer: assessment of mineralization based on alkalinity, inorganic carbon and stable carbon isotope balances

Science.gov (United States)

Hunkeler, Daniel; Höhener, Patrick; Bernasconi, Stefano; Zeyer, Josef

1999-04-01

A concept is proposed to assess in situ petroleum hydrocarbon mineralization by combining data on oxidant consumption, production of reduced species, CH 4, alkalinity and dissolved inorganic carbon (DIC) with measurements of stable isotope ratios. The concept was applied to a diesel fuel contaminated aquifer in Menziken, Switzerland, which was treated by engineered in situ bioremediation. In the contaminated aquifer, added oxidants (O 2 and NO 3-) were consumed, elevated concentrations of Fe(II), Mn(II), CH 4, alkalinity and DIC were detected and the DIC was generally depleted in 13C compared to the background. The DIC production was larger than expected based on the consumption of dissolved oxidants and the production of reduced species. Stable carbon isotope balances revealed that the DIC production in the aquifer originated mainly from microbial petroleum hydrocarbon mineralization, and that geochemical reactions such as carbonate dissolution produced little DIC. This suggests that petroleum hydrocarbon mineralization can be underestimated if it is determined based on concentrations of dissolved oxidants and reduced species.

Characterization of the vadose zone above a shallow aquifer contaminated with gas condensate hydrocarbons

International Nuclear Information System (INIS)

Sublette, K.; Duncan, K.; Thoma, G.; Todd, T.

2002-01-01

A gas production site in the Denver Basin near Ft. Lupton, Colorado has leaked gas condensate hydrocarbons from an underground concrete tank used to store produced water. The leak has contaminated a shallow aquifer. Although the source of pollution has been removed, a plume of hydrocarbon contamination still remains for nearly 46 m from the original source. An extensive monitoring program was conducted in 1993 of the groundwater and saturated sediments. The objective was to determine if intrinsic aerobic or anaerobic bioremediation of hydrocarbons occurred at the site at a rate that would support remediation. Geochemical indicators of hydrogen biodegradation by microorganisms in the saturated zone included oxygen depletion, increased alkalinity, sulfate depletion, methane production and Fe2+ production associated with hydrogen contamination. The presence of sulfate-reducing bacteria and methanogens was also much higher in the contaminated sediments. Degraded hydrocarbon metabolites were found in contaminated groundwater. An extensive characterization of the vadose zone was conducted in which the vadose zone was sample in increments of 15 cm from the surface to the water table at contaminated and non contaminated sites. The samples were tested for individual C3+ hydrocarbons, methane, CO2, total organic carbon, total inorganic carbon, and total petroleum hydrocarbons. The vadose zone consisted of an active and aerobic bioreactor fueled by condensate hydrocarbons transported into the unsaturated zone by evaporation of hydrocarbons at the water table. It was concluded that the unsaturated zone makes an important contribution to the natural attenuation of gas condensate hydrocarbons in the area. 17 refs., 2 tabs., 28 figs

Regeneration strategies of polymers employed in ex-situ remediation of contaminated soil: Bioregeneration versus solvent extraction.

Science.gov (United States)

Mosca Angelucci, Domenica; Tomei, M Concetta

2015-08-15

In this study we evaluated the feasibility of two regeneration strategies of contaminated polymers employed for ex-situ soil remediation in a two-step process. Soil decontamination is achieved by sorption of the pollutants on the polymer beads, which are regenerated in a subsequent step. Tested soil was contaminated with a mixture of 4-chlorophenol and pentachlorophenol, and a commercial polymer, Hytrel, has been employed for extraction. Removal efficiencies of the polymer-soil extraction are in the range of 51-97% for a contact time ≤ 24 h. Two polymer regeneration strategies, solvent extraction and biological regeneration (realized in a two-phase partitioning bioreactor), were tested and compared. Performance was assessed in terms of removal rates and efficiencies and an economic analysis based on the operating costs has been performed. Results demonstrated the feasibility of both regeneration strategies, but the bioregeneration was advantageous in that provided the biodegradation of the contaminants desorbed from the polymer. Practically complete removal for 4-chlorophenol and up to 85% biodegradation efficiency for pentachlorophenol were achieved. Instead, in the solvent extraction, a relevant production (184-831 L kg(pol)(-1)) of a highly polluted stream to be treated or disposed of is observed. The cost analysis of the two strategies showed that the bioregeneration is much more convenient with operating costs of ∼12 €/kg(pol) i.e. more than one order of magnitude lower in comparison to ∼233 €/kg(pol) of the solvent extraction. Copyright © 2015 Elsevier Ltd. All rights reserved.

Assessing the Impact of Chlorinated-Solvent Sites on Metropolitan Groundwater Resources

OpenAIRE

Brusseau, Mark L.; Narter, Matthew

2013-01-01

Chlorinated-solvent compounds are among the most common groundwater contaminants in the U.S.A. The majority of the many sites contaminated by chlorinated-solvent compounds are located in metropolitan areas, and most such areas have one or more chlorinated-solvent contaminated sites. Thus, contamination of groundwater by chlorinated-solvent compounds may pose a potential risk to the sustainability of potable water supplies for many metropolitan areas. The impact of chlorinated-solvent sites on...

78 FR 46447 - Conditional Exclusions From Solid Waste and Hazardous Waste for Solvent-Contaminated Wipes

Science.gov (United States)

2013-07-31

... section 307 of the Clean Water Act (CWA)); A municipal solid waste landfill that is regulated under 40 CFR... laundries and dry cleaners could dispose of sludge from cleaning solvent-contaminated wipes in solid waste landfills if the sludge does not exhibit a hazardous waste characteristic. \\8\\ The Agency stated in the...

Coupling of Realistic Rate Estimates with Genomics for Assessing Contaminant Attenuation and Long-Term Plume Containment

Energy Technology Data Exchange (ETDEWEB)

Colwell, F.S.; Crawford, R.L.; Sorenson, K.

2005-09-01

Acceptance of monitored natural attenuation (MNA) as a preferred treatment technology saves significant site restoration costs for DOE. However, in order to be accepted MNA requires direct evidence of which processes are responsible for the contaminant loss and also the rates of the contaminant loss. Our proposal aims to: 1) provide evidence for one example of MNA, namely the disappearance of the dissolved trichloroethylene (TCE) from the Snake River Plain aquifer (SRPA) at the Idaho National Laboratory’s Test Area North (TAN) site, 2) determine the rates at which aquifer microbes can co-metabolize TCE, and 3) determine whether there are other examples of natural attenuation of chlorinated solvents occurring at DOE sites. To this end, our research has several objectives. First, we have conducted studies to characterize the microbial processes that are likely responsible for the co-metabolic destruction of TCE in the aquifer at TAN (University of Idaho and INL). Second, we are investigating realistic rates of TCE co-metabolism at the low catabolic activities typical of microorganisms existing under aquifer conditions (INL). Using the co-metabolism rate parameters derived in low-growth bioreactors, we will complete the models that predict the time until background levels of TCE are attained in the aquifer at TAN and validate the long-term stewardship of this plume. Coupled with the research on low catabolic activities of co-metabolic microbes we are determining the patterns of functional gene expression by these cells, patterns that may be used to diagnose the co-metabolic activity in the SRPA or other aquifers.

Analysis of Aquifer Response, Groundwater Flow, and PlumeEvolution at Site OU 1, Former Fort Ord, California

Energy Technology Data Exchange (ETDEWEB)

Jordan, Preston D.; Oldenburg, Curtis M.; Su, Grace W.

2005-02-24

This report presents a continuation from Oldenburg et al. (2002) of analysis of the hydrogeology, In-Situ Permeable Flow Sensor (ISPFS) results, aquifer response, and changes in the trichloroethylene (TCE) groundwater plume at Operational Unit 1 (OU 1) adjacent to the former Fritzsche Army Airfield at the former Fort Ord Army Base, located on Monterey Bay in northern Monterey County. Fuels and solvents were burned on a portion of OU 1 called the Fire Drill Area (FDA) during airport fire suppression training between 1962 and 1985. This activity resulted in soil and groundwater contamination in the unconfined A-aquifer. In the late 1980's, soil excavation and bioremediation were successful in remediating soil contamination at the site. Shortly thereafter, a groundwater pump, treat, and recharge system commenced operation. This system has been largely successful at remediating groundwater contamination at the head of the groundwater plume. However, a trichloroethylene (TCE) groundwater plume extends approximately 3000 ft (900 m) to the northwest away from the FDA. In the analyses presented here, we augment our prior work (Oldenburg et al., 2002) with new information including treatment-system totalizer data, recent water-level and chemistry data, and data collected from new wells to discern trends in contaminant migration and groundwater flow that may be useful for ongoing remediation efforts. Some conclusions from the prior study have been modified based on these new analyses, and these are pointed out clearly in this report.

Multi-isotope (carbon and chlorine) analysis for fingerprinting and site characterization at a fractured bedrock aquifer contaminated by chlorinated ethenes

DEFF Research Database (Denmark)

Palau, Jordi; Marchesi, Massimo; Chambon, Julie Claire Claudia

2014-01-01

is located in Spain with contamination resulting in groundwater concentrations of up to 50 mg/L of trichloroethene (TCE), the most abundant chlorinated ethene, and 7 mg/L of tetrachloroethene (PCE). The potential sources of contamination including abandoned barrels, an underground tank, and a disposal lagoon......, showed a wide range in δ13C values from − 15.6 to − 40.5‰ for TCE and from − 18.5 to − 32.4‰ for PCE, allowing the use of isotope fingerprinting for tracing of the origin and migration of these contaminants in the aquifer. In contrast, there is no difference between the δ37Cl values for TCE...

Coupling of Realistic Rate Estimates with Genomics for Assessing Contaminant Attenuation and Long-Term Plume Containment

Energy Technology Data Exchange (ETDEWEB)

Colwell, F. S.; Crawford, R. L.; Sorenson, K.

2005-09-01

Acceptance of monitored natural attenuation (MNA) as a preferred treatment technology saves significant site restoration costs for DOE. However, in order to be accepted MNA requires direct evidence of which processes are responsible for the contaminant loss and also the rates of the contaminant loss. Our proposal aims to: 1) provide evidence for one example of MNA, namely the disappearance of the dissolved trichloroethylene (TCE) from the Snake River Plain aquifer (SRPA) at the Idaho National Laboratory’s Test Area North (TAN) site, 2) determine the rates at which aquifer microbes can co-metabolize TCE, and 3) determine whether there are other examples of natural attenuation of chlorinated solvents occurring at DOE sites. To this end, our research has several objectives. First, we have conducted studies to characterize the microbial processes that are likely responsible for the co-metabolic destruction of TCE in the aquifer at TAN (University of Idaho and INL). Second, we are investigating realistic rates of TCE co-metabolism at the low catabolic activities typical of microorganisms existing under aquifer conditions (INL). Using the co-metabolism rate parameters derived in low-growth bioreactors, we will complete the models that predict the time until background levels of TCE are attained in the aquifer at TAN and validate the long-term stewardship of this plume. Coupled with the research on low catabolic activities of co-metabolic microbes we are determining the patterns of functional gene expression by these cells, patterns that may be used to diagnose the co-metabolic activity in the SRPA or other aquifers. Third, we have systematically considered the aquifer contaminants at different locations in plumes at other DOE sites in order to determine whether MNA is a broadly applicable remediation strategy for chlorinated hydrocarbons (North Wind Inc.). Realistic terms for co-metabolism of TCE will provide marked improvements in DOE’s ability to predict and

Single-well reactive tracer test and stable isotope analysis for determination of microbial activity in a fast hydrocarbon-contaminated aquifer

International Nuclear Information System (INIS)

Burbery, L.; Cassiani, G.; Andreotti, G.; Ricchiuto, T.; Semple, K.T.

2004-01-01

Single-well reactive tracer tests, such as the push-pull test are useful tools for characterising in-situ bioattenuation processes in contaminated aquifers. However, the analytical models that are used to interpret push-pull data may be over-simplified, and potentially overlook important processes responsible for the frequent discrepancy between predicted and observed results obtained from push-pull tests. In this study, the limitations underlying the push-pull test methodology were investigated and were supported with results from a push-pull test conducted in a sulphate-reducing aquifer contaminated by crude oil. Poor ( 20% mass recoveries were achieved. Push-pull test data collected from sulphate-reducing aquifers indicate that the assumption of a well-mixed batch reactor system is incorrect and that reaction rates obtained from push-pull tests in such systems may be affected by the extraction regime implemented. Evidence of microbial respiration of the reactive tracer was provided by stable sulphur isotope analysis, from which an isotope fractionation factor of +9.9±8.1%o was estimated. The stable isotope data support the argument that reaction rates calculated using push-pull tests are not uniformly distributed in space and time and are likely to be influenced by heterogeneities in the flow field. - Reaction rates calculated by push-pull tests are not uniformly distributed in time and space

Risk-Based Management of Contaminated Groundwater: The Role of Geologic Heterogeneity, Exposure and Cancer Risk in Determining the Performance of Aquifer Remediation

International Nuclear Information System (INIS)

Maxwell, R.M.; Carle, S.F.; Tompson, A.F.B.

2000-01-01

The effectiveness of aquifer remediation is typically expressed in terms of a reduction in contaminant concentrations relative to a regulated maximum contaminant level (MCL), and is usually confined by sparse monitoring data and/or simple model calculations. Here, the effectiveness of remediation is examined from a risk-based perspective that goes beyond the traditional MCL concept. A methodology is employed to evaluate the health risk to individuals exposed to contaminated household water that is produced from groundwater. This approach explicitly accounts for differences in risk arising from variability in individual physiology and water use, the uncertainty in estimating chemical carcinogenesis for different individuals, and the uncertainties and variability in contaminant concentrations within groundwater. A hypothetical contamination scenario is developed as a case study in a saturated, alluvial aquifer underlying a real Superfund site. A baseline (unremediated) human exposure and health risk scenario, as induced by contaminated groundwater pumped from this site, is predicted and compared with a similar estimate based upon pump-and-treat exposure intervention. The predicted reduction in risk in the remediation scenario is not an equitable one-that is, it is not uniform to all individuals within a population and varies according to the level of uncertainty in prediction. The importance of understanding the detailed hydrogeologic connections that are established in the heterogeneous geologic regime between the contaminated source, municipal receptors, and remediation wells, and its relationship to this uncertainty is demonstrated. Using two alternative pumping rates, we develop cost-benefit curves based upon reduced exposure and risk to different individuals within the population, under the presence of uncertainty

Numerical simulation of seasonal heat storage in a contaminated shallow aquifer - Temperature influence on flow, transport and reaction processes

Science.gov (United States)

Popp, Steffi; Beyer, Christof; Dahmke, Andreas; Bauer, Sebastian

2015-04-01

The energy market in Germany currently faces a rapid transition from nuclear power and fossil fuels towards an increased production of energy from renewable resources like wind or solar power. In this context, seasonal heat storage in the shallow subsurface is becoming more and more important, particularly in urban regions with high population densities and thus high energy and heat demand. Besides the effects of increased or decreased groundwater and sediment temperatures on local and large-scale groundwater flow, transport, geochemistry and microbiology, an influence on subsurface contaminations, which may be present in the urban surbsurface, can be expected. Currently, concerns about negative impacts of temperature changes on groundwater quality are the main barrier for the approval of heat storage at or close to contaminated sites. The possible impacts of heat storage on subsurface contamination, however, have not been investigated in detail yet. Therefore, this work investigates the effects of a shallow seasonal heat storage on subsurface groundwater flow, transport and reaction processes in the presence of an organic contamination using numerical scenario simulations. A shallow groundwater aquifer is assumed, which consists of Pleistoscene sandy sediments typical for Northern Germany. The seasonal heat storage in these scenarios is performed through arrays of borehole heat exchangers (BHE), where different setups with 6 and 72 BHE, and temperatures during storage between 2°C and 70°C are analyzed. The developing heat plume in the aquifer interacts with a residual phase of a trichloroethene (TCE) contamination. The plume of dissolved TCE emitted from this source zone is degraded by reductive dechlorination through microbes present in the aquifer, which degrade TCE under anaerobic redox conditions to the degradation products dichloroethene, vinyl chloride and ethene. The temperature dependence of the microbial degradation activity of each degradation step is

Susceptibility to saline contamination of coastal confined aquifer of the Uraba banana axis with hydrogeochemical and isotopic techniques

International Nuclear Information System (INIS)

Paredes Zuniga, Vanessa

2010-01-01

The project has covered an area of study of 8916 km 2 is located in the Northwestern part of the Department of Antioquia, Colombia. Interest area is geologically constituted by tertiary sedimentary rocks (T1 and T2) and alluvial deposits (Quaternary). Hydrogeological units, potentially better use of groundwater, have been established for the unit T2 (confined aquifer) and quaternary deposits.) The area has been of 2600 mm/year to 3600 mm/year of average rainfall. The susceptibility to saline contamination has been determined of coastal aquifer of the Uraba banana axis. Hydrochemical and geological information, geophysics, hydraulic and hydrochemical is used improving existing conceptual hydrogeological model. A hydrochemical characterization has been performed to evaluate the processes of salinity in the confined aquifer. The integration of geological information, geophysical and hydrogeological has been methodology used to validate the hydraulic characteristics of the aquifer, its geometry and operation, updating the conceptual hydrogeological model. The use of complementary tools been able to determine and identify processes that may affect natural physico-chemical characteristics of groundwater. The results have showed that salinization processes present in the coastal aquifer of Uraba Banana Axis could be linked to water-rock interaction, to mixtures with water have become saline as a result of transgression - regression processes in the former study. The hydrogeochemical techniques have become a complementary tool to the hydrogeology allowing respond the questions were presented in complex systems, such as the case of coastal aquifers, where sanitation is usually associated with saline intrusion processes and can also be obeying the conjunction with other hydroclimatological and hydrodynamic aspects. (author) [es

Aerobic biodegradation potential of subsurface microorganisms from a jet fuel-contaminated aquifer

International Nuclear Information System (INIS)

Aelion, C.M.; Bradley, P.M.

1991-01-01

Current efforts to remediate subsurface contamination have spurred research in the application of in situ bioremediation. In 1975, a leak of 83,000 gallons (314,189 liters) of jet fuel (JP-4) contaminated a shallow water-table aquifer near North Charleston, S.C. Laboratory experiments were conducted with contaminated sediments to assess the aerobic biodegradation potential of the in situ microbial community. Sediments were incubated with 14 C-labeled organic compounds, and the evolution of 14 CO 2 was measured over time. Gas chromatographic analyses were used to monitor CO 2 production and O 2 consumption under aerobic conditions. Results indicated that the microbes from contaminated sediments remained active despite the potentially toxic effects of JP-4. 14 CO 2 was measured from [ 14 C]glucose respiration in unamended and nitrate-amended samples after 1 day of incubation. Total [ 14 C]glucose metabolism was greater in 1 mM nitrate-amended than in unamended samples because of increased cellular incorporation of 14 C label. [ 14 C]benzene and [ 14 C]toluene were not significantly respired after 3 months of incubation. With the addition of 1 mM NO 3 , CO 2 production measured by gas chromatographic analysis increased linearly during 2 months of incubation at a rte of 0.099 μmol g -1 (dry weight) day -1 while oxygen concentration decreased at a rate of 0.124 μmol g -1 (dry weight) day -1 . With no added nitrate, CO 2 production was not different from that in metabolically inhibited control vials. The results suggest that the in situ microbial community is active despite the JP-4 jet fuel contamination and that biodegradation may be compound specific. Also, the community is strongly nitrogen limited, and nitrogen additions may be required to significantly enhance hydrocarbon biodegradation

Estimating the fates of organic contaminants in an aquifer using QSAR.

Science.gov (United States)

Lim, Seung Joo; Fox, Peter

2013-01-01

The quantitative structure activity relationship (QSAR) model, BIOWIN, was modified to more accurately estimate the fates of organic contaminants in an aquifer. The predictions from BIOWIN were modified to include oxidation and sorption effects. The predictive model therefore included the effects of sorption, biodegradation, and oxidation. A total of 35 organic compounds were used to validate the predictive model. The majority of the ratios of predicted half-life to measured half-life were within a factor of 2 and no ratio values were greater than a factor of 5. In addition, the accuracy of estimating the persistence of organic compounds in the sub-surface was superior when modified by the relative fraction adsorbed to the solid phase, 1/Rf, to that when modified by the remaining fraction of a given compound adsorbed to a solid, 1 - fs.

Enhanced removal of lead from contaminated soil by polyol-based deep eutectic solvents and saponin

Science.gov (United States)

Mukhopadhyay, Soumyadeep; Mukherjee, Sumona; Hayyan, Adeeb; Hayyan, Maan; Hashim, Mohd Ali; Sen Gupta, Bhaskar

2016-11-01

Deep eutectic solvents (DESs) are a class of green solvents analogous to ionic liquids, but less costly and easier to prepare. The objective of this study is to remove lead (Pb) from a contaminated soil by using polyol based DESs mixed with a natural surfactant saponin for the first time. The DESs used in this study were prepared by mixing a quaternary ammonium salt choline chloride with polyols e.g. glycerol and ethylene glycol. A natural surfactant saponin obtained from soapnut fruit pericarp, was mixed with DESs to boost their efficiency. The DESs on their own did not perform satisfactory due to higher pH; however, they improved the performance of soapnut by up to 100%. Pb removal from contaminated soil using mixture of 40% DES-Gly and 1% saponin and mixture of 10% DES-Gly and 2% saponin were above 72% XRD and SEM studies did not detect any major corrosion in the soil texture. The environmental friendliness of both DESs and saponin and their affordable costs merit thorough investigation of their potential as soil washing agents.

Extent and Durability of Contamination of Groundwater and Water Works With The Pesticide Metabolite Bam (2,6 -dichlorbenzamide) Evaluated For Representative Aquifers In Denmark

Science.gov (United States)

Jørgensen, Peter R.; Clausen, Liselotte; Larsen, Flemming

The pesticide metabolite BAM (2,6-dichlorbenzamide) is the most frequently found pesticide contaminant in Danish groundwater. In 1999 BAM was found in 26% of Danish water supply wells and the drinking water standard (0.1 µg/L) was exceeded in 11% of the wells. BAM is a metabolite from the active ingredient dichlobenil (DCB), which was used for non-agricultural total weed protection during 1966 ­ 1997. By using the numerical codes FRAC3Dvs and MODFLOW/MT3D it is the aim of the study to evaluate the extent and durability of the BAM pollution in Danish groundwater and to recommend planning strategies to avoid or minimize BAM in future water supply. The modeling was based on the total amount sold of the DCB (29.000 ton/year) combined with data for sorption and degradation of the DCB and BAM measured from comprehensive laboratory experiments with soil material representing root zone and main aquifer soil types in Denmark. As a main result the laboratory experiments revealed that BAM was only very slowly degraded in the root zone, while no degradation was observed in the sub-soil environments. Combining these model in-put data with representative data for the main aquifer types and overriding fractured clay aquitards, the modeling indicates that more than 99% of infiltrated dichlobenile has been transformed to its metabolite BAM (approximately 500 tons in total), and that currently (year 2001) approximately 100% of this compound appears widely in the groundwater and/or in the above aquitards. The modeling shows that the BAM pollution will appear in the groundwater with a high frequency in extensive parts of Denmark during the following 20 years to more than 100 years. The highest current BAM concentrations, but however also the shortest durability of the BAM pollution, will occur in contaminated aquifers, which are not covered with clay layers. Short durability in such areas is furthermore dependent on the lack of further up-stream BAM sources. The modeling moreover

Three-dimensional analysis of future groundwater flow conditions and contaminant plume transport in the Hanford Site unconfined aquifer system: FY 1996 and 1997 status report

Energy Technology Data Exchange (ETDEWEB)

Cole, C.R.; Wurstner, S.K.; Williams, M.D.; Thorne, P.D.; Bergeron, M.P.

1997-12-01

A three-dimensional numerical model of groundwater flow and transport, based on the Coupled Fluid Energy, and Solute Transport (CFEST) code, was developed for the Hanford Site to support the Hanford Groundwater Project (HGWP), managed by Pacific Northwest National Laboratory. The model was developed to increase the understanding and better forecast the migration of several contaminant plumes being monitored by the HGWP, and to support the Hanford Site Composite Analysis for low-level waste disposal in the 200-Area Plateau. Recent modeling efforts have focused on continued refinement of an initial version of the three-dimensional model developed in 1995 and its application to simulate future transport of selected contaminant plumes in the aquifer system. This version of the model was updated using a more current version of the CFEST code called CFEST96. Prior to conducting simulations of contaminant transport with the three-dimensional model, a previous steady-state, two-dimensional model of the unconfined aquifer system was recalibrated to 1979 water-table conditions with a statistical inverse method implemented in the CFEST-INV computer code. The results of the recalibration were used to refine the three-dimensional conceptual model and to calibrate it with a conceptualization that preserves the two-dimensional hydraulic properties and knowledge of the aquifer`s three-dimensional properties for the same 1979 water-table conditions. The transient behavior of the three-dimensional flow model was also calibrated by adjusting model storage properties (specific yield) until transient water-table predictions approximated observed water-table elevations between 1979 and 1996.

GeoChip-based analysis of microbial functional gene diversity in a landfill leachate-contaminated aquifer

Science.gov (United States)

Lu, Zhenmei; He, Zhili; Parisi, Victoria A.; Kang, Sanghoon; Deng, Ye; Van Nostrand, Joy D.; Masoner, Jason R.; Cozzarelli, Isabelle M.; Suflita, Joseph M.; Zhou, Jizhong

2012-01-01

The functional gene diversity and structure of microbial communities in a shallow landfill leachate-contaminated aquifer were assessed using a comprehensive functional gene array (GeoChip 3.0). Water samples were obtained from eight wells at the same aquifer depth immediately below a municipal landfill or along the predominant downgradient groundwater flowpath. Functional gene richness and diversity immediately below the landfill and the closest well were considerably lower than those in downgradient wells. Mantel tests and canonical correspondence analysis (CCA) suggested that various geochemical parameters had a significant impact on the subsurface microbial community structure. That is, leachate from the unlined landfill impacted the diversity, composition, structure, and functional potential of groundwater microbial communities as a function of groundwater pH, and concentrations of sulfate, ammonia, and dissolved organic carbon (DOC). Historical geochemical records indicate that all sampled wells chronically received leachate, and the increase in microbial diversity as a function of distance from the landfill is consistent with mitigation of the impact of leachate on the groundwater system by natural attenuation mechanisms.

Evaluation of ethyl tert-butyl ether biodegradation in a contaminated aquifer by compound-specific isotope analysis and in situ microcosms

Energy Technology Data Exchange (ETDEWEB)

Bombach, Petra, E-mail: petra.bombach@ufz.de [UFZ – Helmholtz Centre for Environmental Research, Department of Isotope Biogeochemistry, Permoserstrasse 15, D-04318 Leipzig (Germany); Isodetect GmbH Leipzig, Deutscher Platz 5b, D-04103 Leipzig (Germany); Nägele, Norbert [Kuvier the Biotech Company S.L., Ctra. N-I, p.k. 234–P.E. INBISA 23" a, E-09001 Burgos (Spain); Rosell, Mònica [UFZ – Helmholtz Centre for Environmental Research, Department of Isotope Biogeochemistry, Permoserstrasse 15, D-04318 Leipzig (Germany); Grup de Mineralogia Aplicada i Medi Ambient, Departament de Cristallografia, Mineralogia i Dipòsits Minerals, Facultat de Geologia, Universitat de Barcelona (UB), C/Martí i Franquès s/n, 08028 Barcelona (Spain); Richnow, Hans H. [UFZ – Helmholtz Centre for Environmental Research, Department of Isotope Biogeochemistry, Permoserstrasse 15, D-04318 Leipzig (Germany); Fischer, Anko [Isodetect GmbH Leipzig, Deutscher Platz 5b, D-04103 Leipzig (Germany)

2015-04-09

Highlights: • In situ biodegradation of ETBE was investigated in a fuel contaminated aquifer. • Degradation was studied by CSIA and in situ microcosms in combination with TLFA-SIP. • ETBE was degraded when ETBE was the main groundwater contaminant. • ETBE was also degraded in the presence of BTEX and MTBE. • Hydrochemical analysis indicated aerobic and anaerobic ETBE biodegradation. - Abstract: Ethyl tert-butyl ether (ETBE) is an upcoming groundwater pollutant in Europe whose environmental fate has been less investigated, thus far. In the present study, we investigated the in situ biodegradation of ETBE in a fuel-contaminated aquifer using compound-specific stable isotope analysis (CSIA), and in situ microcosms in combination with total lipid fatty acid (TLFA)-stable isotope probing (SIP). In a first field investigation, CSIA revealed insignificant carbon isotope fractionation, but low hydrogen isotope fractionation of up to +14‰ along the prevailing anoxic ETBE plume suggesting biodegradation of ETBE. Ten months later, oxygen injection was conducted to enhance the biodegradation of petroleum hydrocarbons (PH) at the field site. Within the framework of this remediation measure, in situ microcosms loaded with [{sup 13}C{sub 6}]-ETBE (BACTRAP{sup ®}s) were exposed for 119 days in selected groundwater wells to assess the biodegradation of ETBE by TLFA-SIP under the following conditions: (i) ETBE as main contaminant; (ii) ETBE as main contaminant subjected to oxygen injection; (iii) ETBE plus other PH; (iv) ETBE plus other PH subjected to oxygen injection. Under all conditions investigated, significant {sup 13}C-incorporation into microbial total lipid fatty acids extracted from the in situ microcosms was found, providing clear evidence of ETBE biodegradation.

Evaluation of ethyl tert-butyl ether biodegradation in a contaminated aquifer by compound-specific isotope analysis and in situ microcosms

International Nuclear Information System (INIS)

Bombach, Petra; a, E-09001 Burgos (Spain))" data-affiliation=" (Kuvier the Biotech Company S.L., Ctra. N-I, p.k. 234–P.E. INBISA 23a, E-09001 Burgos (Spain))" >Nägele, Norbert; Rosell, Mònica; Richnow, Hans H.; Fischer, Anko

2015-01-01

Highlights: • In situ biodegradation of ETBE was investigated in a fuel contaminated aquifer. • Degradation was studied by CSIA and in situ microcosms in combination with TLFA-SIP. • ETBE was degraded when ETBE was the main groundwater contaminant. • ETBE was also degraded in the presence of BTEX and MTBE. • Hydrochemical analysis indicated aerobic and anaerobic ETBE biodegradation. - Abstract: Ethyl tert-butyl ether (ETBE) is an upcoming groundwater pollutant in Europe whose environmental fate has been less investigated, thus far. In the present study, we investigated the in situ biodegradation of ETBE in a fuel-contaminated aquifer using compound-specific stable isotope analysis (CSIA), and in situ microcosms in combination with total lipid fatty acid (TLFA)-stable isotope probing (SIP). In a first field investigation, CSIA revealed insignificant carbon isotope fractionation, but low hydrogen isotope fractionation of up to +14‰ along the prevailing anoxic ETBE plume suggesting biodegradation of ETBE. Ten months later, oxygen injection was conducted to enhance the biodegradation of petroleum hydrocarbons (PH) at the field site. Within the framework of this remediation measure, in situ microcosms loaded with [ 13 C 6 ]-ETBE (BACTRAP ® s) were exposed for 119 days in selected groundwater wells to assess the biodegradation of ETBE by TLFA-SIP under the following conditions: (i) ETBE as main contaminant; (ii) ETBE as main contaminant subjected to oxygen injection; (iii) ETBE plus other PH; (iv) ETBE plus other PH subjected to oxygen injection. Under all conditions investigated, significant 13 C-incorporation into microbial total lipid fatty acids extracted from the in situ microcosms was found, providing clear evidence of ETBE biodegradation

Enhanced reductive dechlorination in clay till contaminated with chlorinated solvents

DEFF Research Database (Denmark)

Damgaard, Ida

Chlorinated solvents are among the most frequently found contaminants in groundwater. In fractured media, chlorinated ethenes and ethanes are transported downwards through preferential pathways with subsequent diffusion into the sediment matrix. Due to slow back diffusion it can serve as a long...... (direct push delivery, Gl. Kongevej). Degradation of chlorinated ethenes (and ethanes) in the clay till matrix and in embedded high permeability features was investigated by high resolution sampling of intact cores combined with groundwater sampling. An integrated approach using chemical analysis...... (hydraulic fracturing with gravitational injection and direct push delivery) were therefore tested in clay till by injection of amendment-comparable tracers to investigate the possibility to overcome diffusion limitations in the low permeability matrix. The study of hydraulic fracturing demonstrated...

Factors Affecting Public-Supply Well Vulnerability in Two Karst Aquifers

OpenAIRE

Musgrove, MaryLynn; Katz, Brian G; Fahlquist, Lynne S; Crandall, Christy A; Lindgren, Richard J

2014-01-01

Karst aquifers occur in a range of climatic and geologic settings. Nonetheless, they are commonly characterized by their vulnerability to water-quality impairment. Two karst aquifers, the Edwards aquifer in south-central Texas and the Upper Floridan aquifer in western Florida, were investigated to assess factors that control the movement of contaminants to public-supply wells (PSWs). The geochemistry of samples from a selected PSW or wellfield in each aquifer was compared with that from nearb...

Aquifer Sampling Tube Completion Report: 100 Area and Hanford Townsite Shorelines

International Nuclear Information System (INIS)

Peterson, R.E.; Borghese, J.V.; Erb, D.B.

1998-02-01

Groundwater contamination is known or suspected along the Hanford Site shoreline of the Columbia River adjacent to the retired reactor areas. Along the shoreline away from the reactor areas, where contamination is presumed to be absent, monitoring sites are frequently widely spaced or unavailable to confirm the presumption. Previous characterizations of contamination near the river have relied on data from a limited number of near-river wells, contaminant plume migration predictions, and river bank seepage sampling to anticipate shoreline conditions. In recent years, new methods have been developed to obtain groundwater samples from the aquifer near the groundwater/river water interface. These methods include using (1) divers to obtain samples of pore water from riverbed sediment and (2) sampling tubes that are driven into the aquifer at the shoreline. The latter method also permits sampling the aquifer at multiple depths, which helps to determine the thickness of the potentially contaminated groundwater layer that discharges into the river

The use of nitrate isotopes to identify contamination sources in the Bou-Areg aquifer (Morocco)

Energy Technology Data Exchange (ETDEWEB)

Re, Viviana [Ca' Foscari University of Venice, Department of Molecular Sciences and Nanosystems, Dorsoduro 2137, Venice, 30123 (Italy); Sacchi, Elisa [University of Pavia, Department of Earth and Environmental Sciences, Via Ferrata 1, Pavia, 27100 (Italy); Allais, Enrico [ISO4 s.n.c., Via Ferrata 1, Pavia, 27100 (Italy)

2013-07-01

The Bou-Areg coastal aquifer (Morocco) is affected by high nitrate levels in groundwater, with possible consequences for the natural environment and human health. The use of environmental tracers, including δ{sup 15}NNO{sub 3} and δ{sup 18}ONO{sub 3}, allowed identifying the main sources of nitrate contamination in groundwater samples collected in 2010. These are manure and septic effluents, especially in urban areas, and synthetic fertilizers in agricultural areas. This work represents a preliminary step for a more detailed nitrate vulnerability assessment to support groundwater management and protection in the studied region. (authors)

Modeling subsurface contamination at Fernald

International Nuclear Information System (INIS)

Jones, B.W.; Flinn, J.C.; Ruwe, P.R.

1994-01-01

The Department of Energy's Fernald site is located about 20 miles northwest of Cincinnati. Fernald produced refined uranium metal products from ores between 1953 and 1989. The pure uranium was sent to other DOE sites in South Carolina, Tennessee, Colorado,and Washington in support of the nation's strategic defense programs. Over the years of large-scale uranium production, contamination of the site's soil and groundwater occurred.The contamination is of particular concern because the Fernald site is located over the Great Miami Aquifer, a designated sole-source drinking water aquifer. Contamination of the aquifer with uranium was found beneath the site, and migration of the contamination had occurred well beyond the site's southern boundary. As a result, Fernald was placed on the National Priorities (CERCLA/Superfund) List in 1989. Uranium production at the site ended in 1989,and Fernald's mission has been changed to one of environmental restoration. This paper presents information about computerized modeling of subsurface contamination used for the environmental restoration project at Fernald

Isotope chemistry of an extensively nitrate-contaminated urban aquifer

Science.gov (United States)

Kracht, O.; de Souza, L. C.; de Queiros, M. A.; Stegemann, C.; Hunziker, J.

2003-04-01

The supply of drinking water for the approximately 800.000 inhabitants of the city of Natal (Rio Grande do Norte, Brazil) is strongly dependent on the use of local groundwater from the Barreiras Aquifer. Over 70 % of the public production are served by a system of about 130 tubular wells, that are distributed all over the urban area. Yet, no groundwater protection zones have been declared. In addition, a comparable number of private wells also depend on the cities underground water resources. Depending on the local topography, the groundwater table is located several tens of meters below surface. Useable groundwater occurrences are bound to an up to hundred meters thick series of unconsolidated clastic sediments from the younger tertiary (Barreiras Formation), that is underlain by less permeable cretaceous carbonates. Natals topography is dominated by impressive quaternary dunes formations, that play an important role for the infiltration of rain as the only source of recharge for the local groundwater. During the last decades, an extensive and rapidly growing groundwater-contamination with up to over 100 mg/l nitrate was observed by the local authorities. Hydrochemical data indicate this deterioration to be due to a massive spill of sanitary effluents over septic pits, as only 20 % of the city is yet served by a sewer system. The isotopic composition of Natals groundwater shows only small variations, with an average δ18O value of -2,3 per mill and δ2H value of -10,5 per mill vs. SMOW. Its origin from recent local precipitation is revealed by a good correspondence with the annual weighted means for precipitation in Ceara Mirim (nearest GNIP station, situated 45 km NE of Natal). In contrast, a set of samples from different regional surface waters indicated a strong evaporation trend with systematic enrichment in the oxygen and hydrogen isotopic composition. Samples from 33 production wells with a wide variation of nitrate concentrations were investigated for their

Fate of sulfamethoxazole, 4-nonylphenol, and 17β-estradiol in groundwater contaminated by wastewater treatment plant effluent

Science.gov (United States)

Barber, Larry B.; Keefe, Steffanie H.; LeBlanc, Denis R.; Bradley, Paul M.; Chapelle, Francis H.; Meyer, Michael T.; Loftin, Keith A.; Koplin, Dana W.; Rubio, Fernando

2009-01-01

Organic wastewater contaminants (OWCs) were measured in samples collected from monitoring wells located along a 4.5-km transect of a plume of groundwater contaminated by 60 years of continuous rapid infiltration disposal of wastewater treatment plant effluent. Fifteen percent of the 212 OWCs analyzed were detected, including the antibiotic sulfamethoxazole (SX), the nonionic surfactant degradation product 4-nonylphenol (NP), the solvent tetrachloroethene (PCE), and the disinfectant 1,4-dichlorobenzene (DCB). Comparison of the 2005 sampling results to data collected from the same wells in 1985 indicates that PCE and DCB are transported more rapidly in the aquifer than NP, consistent with predictions based on compound hydrophobicity. Natural gradient in situ tracer experiments were conducted to evaluate the subsurface behavior of SX, NP, and the female sex hormone 17β-estradiol (E2) in two oxic zones in the aquifer: (1) a downgradient transition zone at the interface between the contamination plume and the overlying uncontaminated groundwater and (2) a contaminated zone located beneath the infiltration beds, which have not been loaded for 10 years. In both zones, breakthrough curves for the conservative tracer bromide (Br−) and SX were nearly coincident, whereas NP and E2 were retarded relative to Br− and showed mass loss. Retardation was greater in the contaminated zone than in the transition zone. Attenuation of NP and E2 in the aquifer was attributed to biotransformation, and oxic laboratory microcosm experiments using sediments from the transition and contaminated zones show that uniform-ring-labeled 14C 4-normal-NP was biodegraded more rapidly (30−60% recovered as 14CO2 in 13 days) than 4-14C E2 (20−90% recovered as 14CO2in 54 days). There was little difference in mineralization potential between sites.

Spore-forming, Desulfosporosinus-like sulphate-reducing bacteria from a shallow aquifer contaminated with gasoline.

Science.gov (United States)

Robertson, W J; Franzmann, P D; Mee, B J

2000-02-01

Previous studies on the geochemistry of a shallow unconfined aquifer contaminated with hydrocarbons suggested that the degradation of some hydrocarbons was linked to bacterial sulphate reduction. There was attenuation of naphthalene, 1,3,5-trimethylbenzene (TMB), toluene, p-xylene and ethylbenzene in the groundwater with concomitant loss of sulphate. Here, the recovery of eight strains of sulphate-reducing bacteria (SRB) from the contaminated site is reported. All were straight or curved rod-shaped cells which formed endospores. Amplification and sequencing of the 16S rDNA indicated that the strains were all sulphate reducers of the Gram-positive line of descent, and were most closely related to Desulfosporosinus (previously Desulfotomaculum) orientis DSM 8344 (97-98.9% sequence similarity). The strains clustered in three phylogenetic groups based on 16S rRNA sequences. Whole cell fatty acid compositions were similar to those of D. orientis DSM 8344, and were consistent with previous studies of fatty acids in soil and groundwater from the site. Microcosms containing groundwater from this aquifer indicated a role for sulphate reduction in the degradation of [ring-UL-14C]toluene, but not for the degradation of [UL-14C]benzene which could also be degraded by the microcosms. Adding one of the strains that was isolated from the groundwater (strain T2) to sulphate-enriched microcosms increased the rate of toluene degradation four- to 10-fold but had no effect on the rate of benzene degradation. The addition of molybdate, an inhibitor of sulphate reduction, to the groundwater samples decreased the rate of toluene mineralization. There was no evidence to support the mineralization of [UL-14C]benzene, [ring-UL-14C]toluene or unlabelled m-xylene, p-xylene, ethylbenzene, TMB or naphthalene by any of the strains in pure culture. Growth of all the strains was completely inhibited by 100 micromol l-1 TMB.

Assessing the vulnerability of public-supply wells to contamination—Edwards aquifer near San Antonio, Texas

Science.gov (United States)

Jagucki, Martha L.; Musgrove, MaryLynn; Lindgren, Richard J.; Fahlquist, Lynne; Eberts, Sandra M.

2011-01-01

This fact sheet highlights findings from the vulnerability study of a public-supply well field in San Antonio, Texas. The well field consists of six production wells that tap the Edwards aquifer. Typically, one or two wells are pumped at a time, yielding an average total of 20-21 million gallons per day. Water samples were collected from public-supply wells in the well field and from monitoring wells installed along general directions of flow to the well field. Samples from the well field contained some constituents of concern for drinking-water quality, including nitrate; the pesticide compounds atrazine, deethylatrazine, and simazine; and the volatile organic compounds tetrachloroethene (also called perchloroethene, or PCE), chloroform, bromoform, and dibromochloromethane. These constituents were detected in untreated water at concentrations much less than established drinking-water standards, where such standards exist. Overall, the study findings point to four primary factors that affect the movement and fate of contaminants and the vulnerability of the public-supply well field in San Antonio, Texas: (1) groundwater age (how long ago water entered, or recharged, the aquifer), (2) fast pathways for flow of groundwater through features formed or enlarged by dissolution of bedrock, (3) recharge characteristics of the aquifer, and (4) natural geochemical processes within the aquifer. A computer-model simulation of groundwater flow and transport was used to estimate the traveltime (or age) of water particles entering public-supply well W4 in the well field. Modeled findings show that almost half of the water reaching the public-supply well is less than 2 years old. Such a large percentage of very young water indicates that (1) contaminants entering the aquifer may be transported rapidly to the well, (2) there is limited time for chemical reactions to occur in the aquifer that may attenuate contaminants, and (3) should recharge water become contaminated with

Bioavailability and biodegradation of weathered diesel fuel in aquifer material under denitrifying conditions

International Nuclear Information System (INIS)

Bregnard, T.P.A.; Hoehener, P.; Zeyer, J.

1998-01-01

During the in situ bioremediation of a diesel fuel-contaminated aquifer in Menziken, Switzerland, aquifer material containing weathered diesel fuel (WDF) and indigenous microorganisms was excavated. This material was used to identify factors limiting WDF biodegradation under denitrifying conditions. Incubations of this material for 360 to 390 d under denitrifying conditions resulted in degradation of 23% of the WDF with concomitant consumption of NO 3 - and production of inorganic carbon. The biodegradation of WDF and the rate of NO 3 - consumption was stimulated by agitation of the microcosms. Biodegradation was not stimulated by the addition of a biosurfactant (rhamnolipids) or a synthetic surfactant (Triton X-100) at concentrations above their critical micelle concentrations. The rhamnolipids were biodegraded preferentially to WDF, whereas Triton X-100 was not degraded. Both surfactants reduced the surface tension of the growth medium from 72 to <35 dynes/cm and enhanced the apparent aqueous solubility of the model hydrocarbon n-hexadecane by four orders of magnitude. Solvent-extracted WDF, added at a concentration equal to that already present in the aquifer material, was also biodegraded by the microcosms, but not at a higher rate than the WDF already present in the material. The results show that the denitrifying biodegradation of WDF is not necessarily limited by bioavailability but rather by the inherent recalcitrance of WDF

Method of and apparatus for cleaning garments and soft goods contaminated with nuclear, chemical and/or biological contaminants

International Nuclear Information System (INIS)

Fowler, D.E.

1989-01-01

A method is described for decontaminating garments, soft good or mixtures thereof contaminated with radioactive particulates, toxin, chemical, and biological contaminants comprising the steps of: (a) depositing contaminated garments, soft goods or mixtures thereof in a cleaning drum; (b) charging the drum with a cleaning solvent in which the chemical contaminants are soluble; (c) agitating the drum during a wash cycle to separate radioactive, toxin, biological particulate matter of mixtures thereof from the garments; (d) draining the drum of the dry cleaning solvent which contains suspended particulate contaminants and dissolved chemical contaminants; (e) contacting the drained solvent with both a neutralizing agent and an oxidizing agent, the neutralizing agent being selected from the group consisting of sodium hydroxide, potassium hydroxide and mixtures thereof and having a concentration greater than one (1.0) normal; (f) rinsing the garments, soft goods or mixtures thereof by circulating clean solvent from a solvent tank through the drum thereby effecting additional removal and flushing of particulate and chemical contaminants; (g) filtering the circulated solvent to remove the particulate material suspended in the solvent prior to addition to the drum; and (h) preferentially adsorbing the chemical contaminants dissolved in the circulated solvent prior to addition to the drum

The Role of Attached and Free-Living Bacteria in Biodegradation in Karst Aquifers

Directory of Open Access Journals (Sweden)

Ahmad Kheder

2011-12-01

Full Text Available Natural attenuation of groundwater contamination occurs at some level for all aquifers impacted with organic contaminants. The issues regarding natural attenuation are whether it takes place at a sufficient rate to be protective of human health and the environment. Implementation of a Monitored Natural Attenuation (MNA remedial alternative for groundwater requires parties responsible for the contamination to demonstrate to regulators and the public that MNA is protective at a given site. Analysis of MNA for remediation of karst aquifers is hampered by a lack of understanding of biodegradation in karst environments. The lack of studies examining biodegradation in karst aquifers may in large part be due to the widespread perception that contaminants are rapidly flushed out of karst aquifers resulting in insufficient residence times for contaminants to biodegrade. In highly developed and well-connected conduit systems, the rate of contaminant migration is perceived to be much faster than the rate of biodegradation. This perception of contaminant transport is largely incorrect. Tracer studies for karst aquifers often indicate that these aquifers are characterized by diverse flow regimes and storage capabilities. Additionally, it is also believed that if bioremediation in bedrock aquifers is dependent upon contact between surface-attached bacteria and contaminants, then bioremediation would be limited by the low surface-area-to-volume ratio (SA/V of karst aquifers. A quantitative basis, however, for accepting or rejecting the assumption that attached bacteria dominate the biodegradation process in karst conduits has not been shown. The objective of this research was to determine if free-living karst bacteria from contributed as much to toluene biodegradation as attached bacteria. This is an important area of research. Research indicates bacteria are both attached and free-living in karst aquifers and it is unrealistic to think that only the attached

Water-quality characteristics of quaternary unconsolidated-deposit aquifers and lower tertiary aquifers of the Bighorn Basin, Wyoming and Montana, 1999-2001

Science.gov (United States)

Bartos, Timothy T.; Eddy-Miller, Cheryl A.; Norris, Jody R.; Gamper, Merry E.; Hallberg, Laura L.

2004-01-01

As part of the Yellowstone River Basin National Water Quality Assessment study, ground-water samples were collected from Quaternary unconsolidated-deposit and lower Tertiary aquifers in the Bighorn Basin of Wyoming and Montana from 1999 to 2001. Samples from 54 wells were analyzed for physical characteristics, major ions, trace elements, nutrients, dissolved organic carbon, radionuclides, pesticide compounds, and volatile organic compounds (VOCs) to evaluate current water-quality conditions in both aquifers. Water-quality samples indicated that waters generally were suitable for most uses, and that natural conditions, rather than the effects of human activities, were more likely to limit uses of the waters. Waters in both types of aquifers generally were highly mineralized, and total dissolved-solids concentrations frequently exceeded the U.S. Environmental Protection Agency (USEPA) Secondary Maximum Contaminant Level (SMCL) of 500 milligrams per liter (mg/L). Because of generally high mineralization, waters from nearly one-half of the samples from Quaternary aquifers and more than one-half of the samples from lower Tertiary aquifers were not classified as fresh (dissolved-solids concentration were not less than 1,000 mg/L). The anions sulfate, fluoride, and chloride were measured in some ground-water samples at concentrations greater than SMCLs. Most waters from the Quaternary aquifers were classified as very hard (hardness greater than 180 mg/L), but hardness varied much more in waters from the lower Tertiary aquifers and ranged from soft (less than 60 mg/L) to very hard (greater than 180 mg/L). Major-ion chemistry varied with dissolved-solids concentrations. In both types of aquifers, the predominant anion changes from bicarbonate to sulfate with increasing dissolved-solids concentrations. Samples from Quaternary aquifers with fresh waters generally were calcium-bicarbonate, calcium-sodium-bicarbonate, and calcium-sodium-sulfate-bicarbonate type waters, whereas

Development and validation of a model of bio-barriers for remediation of Cr(VI) contaminated aquifers using laboratory column experiments.

Science.gov (United States)

Shashidhar, T; Bhallamudi, S Murty; Philip, Ligy

2007-07-16

Bench scale transport and biotransformation experiments and mathematical model simulations were carried out to study the effectiveness of bio-barriers for the containment of hexavalent chromium in contaminated confined aquifers. Experimental results showed that a 10cm thick bio-barrier with an initial biomass concentration of 0.205mg/g of soil was able to completely contain a Cr(VI) plume of 25mg/L concentration. It was also observed that pore water velocity and initial biomass concentration are the most significant parameters in the containment of Cr(VI). The mathematical model developed is based on one-dimensional advection-dispersion reaction equations for Cr(VI) and molasses in saturated, homogeneous porous medium. The transport of Cr(VI) and molasses is coupled with adsorption and Monod's inhibition kinetics for immobile bacteria. It was found that, in general, the model was able to simulate the experimental results satisfactorily. However, there was disparity between the numerically simulated and experimental breakthrough curves for Cr(VI) and molasses in cases where there was high clay content and high microbial activity. The mathematical model could contribute towards improved designs of future bio-barriers for the remediation of Cr(VI) contaminated aquifers.

Water-quality observations of the San Antonio segment of the Edwards aquifer, Texas, with an emphasis on processes influencing nutrient and pesticide geochemistry and factors affecting aquifer vulnerability, 2010–16

Science.gov (United States)

Opsahl, Stephen P.; Musgrove, MaryLynn; Mahler, Barbara J.; Lambert, Rebecca B.

2018-06-07

As questions regarding the influence of increasing urbanization on water quality in the Edwards aquifer are raised, a better understanding of the sources, fate, and transport of compounds of concern in the aquifer—in particular, nutrients and pesticides—is needed to improve water management decision-making capabilities. The U.S. Geological Survey, in cooperation with the San Antonio Water System, performed a study from 2010 to 2016 to better understand how water quality changes under a range of hydrologic conditions and in contrasting land-cover settings (rural and urban) in the Edwards aquifer. The study design included continuous hydrologic monitoring, continuous water-quality monitoring, and discrete sample collection for a detailed characterization of water quality at a network of sites throughout the aquifer system. The sites were selected to encompass a “source-to-sink” (that is, from aquifer recharge to aquifer discharge) approach. Network sites were selected to characterize rainfall, recharging surface water, and groundwater; groundwater sites included wells in the unconfined part of the aquifer (unconfined wells) and in the confined part of the aquifer (confined wells) and a major discharging spring. Storm-related samples—including rainfall samples, stormwater-runoff (surface-water) samples, and groundwater samples—were collected to characterize the aquifer response to recharge.Elevated nitrate concentrations relative to national background values and the widespread detection of pesticides indicate that the Edwards aquifer is vulnerable to contamination and that vulnerability is affected by factors such as land cover, aquifer hydrogeology, and changes in hydrologic conditions. Greater vulnerability of groundwater in urban areas relative to rural areas was evident from results for urban groundwater sites, which generally had higher nitrate concentrations, elevated δ15N-nitrate values, a greater diversity of pesticides, and higher pesticide

Upper Basalt-Confined Aquifer System in the Southern Hanford Site

International Nuclear Information System (INIS)

Thorne, P.

1999-01-01

The 1990 DOE Tiger Team Finding GW/CF-202 found that the hydrogeologic regime at the Hanford Site was inadequately characterized. This finding also identified the need for completing a study of the confined aquifer in the central and southern portions of the Hanford Site. The southern portion of the site is of particular interest because hydraulic-head patterns in the upper basalt-confined aquifer system indicate that groundwater from the Hanford central plateau area, where contaminants have been found in the aquifer, flows southeast toward the southern site boundary. This results in a potential for offsite migration of contaminants through the upper basalt-confined aquifer system. Based on the review presented in this report, available hydrogeologic characterization information for the upper basalt-confined aquifer system in this area is considered adequate to close the action item. Recently drilled offsite wells have provided additional information on the structure of the aquifer system in and near the southern part of the Hanford Site. Information on hydraulic properties, hydrochemistry, hydraulic heads and flow directions for the upper basalt-confined aquifer system has been re-examined and compiled in recent reports including Spane and Raymond (1993), Spane and Vermeul ( 1994), and Spane and Webber (1995)

Geochemical evolution processes and water-quality observations based on results of the National Water-Quality Assessment Program in the San Antonio segment of the Edwards aquifer, 1996-2006

Science.gov (United States)

Musgrove, MaryLynn; Fahlquist, Lynne; Houston, Natalie A.; Lindgren, Richard J.; Ging, Patricia B.

2010-01-01

increase along flow paths; results for samples of Edwards aquifer groundwater show an increase from shallow/urban unconfined, to unconfined, to confined groundwater categories. These differences are consistent with longer residence times and greater extents of water-rock interaction controlling fluid compositions as groundwater evolves from shallow unconfined groundwater to deeper confined groundwater. Results for stable isotopes of hydrogen and oxygen indicate specific geochemical processes affect some groundwater samples, including mixing with downdip saline water, mixing with recent recharge associated with tropical cyclonic storms, or mixing with recharge water than has undergone evaporation. The composition of surface water recharging the aquifer, as well as mixing with downdip water from the Trinity aquifer or the saline zone, also might affect water quality. A time-series record (1938-2006) of discharge at Comal Springs, one of the major aquifer discharge points, indicates an upward trend for nitrate and chloride concentrations, which likely reflects anthropogenic activities. A small number of organic contaminants were routinely or frequently detected in Edwards aquifer groundwater samples. These were the pesticides atrazine, its degradate deethylatrazine, and simazine; the drinking-water disinfection byproduct chloroform; and the solvent tetrachloroethene. Detection of these contaminants was most frequent in samples of the shallow/urban unconfined groundwater category and least frequent in samples of the unconfined groundwater category. Results indicate that the shallow/urban unconfined part of the aquifer is most affected by anthropogenic contaminants and the unconfined part of the aquifer is the least affected. The high frequency of detection for these anthropogenic contaminants aquifer-wide and in samples of deep, confined groundwater indicates that the entire aquifer is susceptible to water-quality changes as a result of anthropogenic activities. L

Industrial rag cleaning process for the environmentally safe removal of petroleum-based solvents

International Nuclear Information System (INIS)

Fierro, J.V.

1993-01-01

A process for the cleaning of industrial rags contaminated with environmentally unsafe petroleum-based solvent is described, comprising the step of: (a) placing a load of the industrial rags in a mechanically driven rotary drum; (b) revolving the drum at a high speed sufficient to physically extract liquid petroleum-based solvent contaminate from the industrial rags; (c) routing the extracted petroleum-based solvent contaminate from the rotary drum to a waste solvent collection line for environmentally safe disposal; (d) revolving the rotary drum to cause a tumbling of the industrial rags while maintaining the temperature within the drum at below the flash point of the petroleum-based solvent; (e) intermittently forcing cold air and hot air through the rotary drum to vaporize solvent from the industrial rags; (f) routing the vaporized petroleum-based solvent contaminant from the rotary drum to a condenser wherein the petroleum-based solvent contaminate is condensed and thereafter further routing said condensed solvent to a waste collection line for environmentally safe disposal; and (g) cleaning the industrial rags in the presence of a dry cleaning solvent to remove residual petroleum-based solvents and soil

Multitracer test for the determination of transport and in-situ degradation of organic micro-contaminants in karst aquifers on the example of caffeine

Science.gov (United States)

Hillebrand, O.; Nödler, K.; Licha, T.; Geyer, T.

2012-04-01

The application of organic micro-contaminants as indicators for contamination sources in aquifers and surface-water bodies has been increasingly discussed in the literature over the last years. One of the proposed substances was caffeine. It served as indicator for wastewater-leakage to various systems. As well, wastewater volumes could be estimated from caffeine concentrations. Although caffeine is known to be degradable, the degradation rates are normally only determined from mass balances or laboratory experiments. Degradation rates obtained from mass balances are relatively uncertain, as the input-function is difficult to be assessed. Laboratory experiments are hardly capable to consider the full complexity of natural systems and can rarely be transferred to those. To solve this problem, in-situ degradation rates of reactive indicators have to be determined. Especially multitracer tests can be used to access compound-specific transport parameters and degradation rates, relative to conservative tracers. A multitracer test with caffeine and uranine has been performed in a karst system (catchment of the Gallusquelle spring, SW Germany). From the breakthrough curves of the tracers, the transport behavior and the in-situ degradation rate of caffeine could be deduced. The tracers were injected into a sinkhole with a linear distance of 3000 m to the spring. The mean residence time of the tracers was found to be 84 h at a flow velocity of 35 m/h. Throughout the whole experiment, the spring discharge was constant at 187 L/s. Uranine served as conservative reference-tracer for the calibration of a one-dimensional transport model with respect to solute-unspecific parameters. Relative to that, the tracer breakthrough curve of caffeine was interpreted. As solute-specific parameters the retardation coefficient as well as degradation rate of caffeine in the investigated karst aquifer could be determined. The results indicate, that caffeine is slightly retarded in the

Hydrochemistry and hydrogeologic conditions within the Hanford Site upper basalt confined aquifer system

International Nuclear Information System (INIS)

Spane, F.A. Jr.; Webber, W.D.

1995-09-01

As part of the Hanford Site Ground-Water Surveillance Project, Flow System Characterization Task. Pacific Northwest Laboratory examines the potential for offsite migration of contamination within the upper basalt confined aquifer system for the US Department of Energy (DOE). As part of this activity, groundwater samples were collected over the past 2 years from selected wells completed in the upper Saddle Mountains Basalt. The hydrochemical and isotopic information obtained from these groundwater samples provides hydrologic information concerning the aquifer-flow system. Ideally, when combined with other hydrologic property information, hydrochemical and isotopic data can be used to evaluate the origin and source of groundwater, areal groundwater-flow patterns, residence and groundwater travel time, rock/groundwater reactions, and aquifer intercommunication for the upper basalt confined aquifer system. This report presents the first comprehensive Hanford Site-wide summary of hydrochemical properties for the upper basalt confined aquifer system. This report provides the hydrogeologic characteristics (Section 2.0) and hydrochemical properties (Section 3.0) for groundwater within this system. A detailed description of the range of the identified hydrochemical parameter subgroups for groundwater in the upper basalt confined aquifer system is also presented in Section 3.0. Evidence that is indicative of aquifer contamination/aquifer intercommunication and an assessment of the potential for offsite migration of contaminants in groundwater within the upper basalt aquifer is provided in Section 4.0. The references cited throughout the report are given in Section 5.0. Tables that summarize groundwater sample analysis results for individual test interval/well sites are included in the Appendix

Redox Conditions in Selected Principal Aquifers of the United States

Science.gov (United States)

McMahon, P.B.; Cowdery, T.K.; Chapelle, F.H.; Jurgens, B.C.

2009-01-01

Reduction/oxidation (redox) processes affect the quality of groundwater in all aquifer systems. Redox processes can alternately mobilize or immobilize potentially toxic metals associated with naturally occurring aquifer materials, contribute to the degradation or preservation of anthropogenic contami-nants, and generate undesirable byproducts, such as dissolved manganese (Mn2+), ferrous iron (Fe2+), hydrogen sulfide (H2S), and methane (CH4). Determining the kinds of redox processes that occur in an aquifer system, documenting their spatial distribution, and understanding how they affect concentrations of natural or anthropogenic contaminants are central to assessing and predicting the chemical quality of groundwater. This Fact Sheet extends the analysis of U.S. Geological Survey authors to additional principal aquifer systems by applying a framework developed by the USGS to a larger set of water-quality data from the USGS national water databases. For a detailed explanation, see the 'Introduction' in the Fact Sheet.

Determination of dominant biogeochemical processes in a contaminated aquifer-wetland system using multivariate statistical analysis

Science.gov (United States)

Baez-Cazull, S. E.; McGuire, J.T.; Cozzarelli, I.M.; Voytek, M.A.

2008-01-01

Determining the processes governing aqueous biogeochemistry in a wetland hydrologically linked to an underlying contaminated aquifer is challenging due to the complex exchange between the systems and their distinct responses to changes in precipitation, recharge, and biological activities. To evaluate temporal and spatial processes in the wetland-aquifer system, water samples were collected using cm-scale multichambered passive diffusion samplers (peepers) to span the wetland-aquifer interface over a period of 3 yr. Samples were analyzed for major cations and anions, methane, and a suite of organic acids resulting in a large dataset of over 8000 points, which was evaluated using multivariate statistics. Principal component analysis (PCA) was chosen with the purpose of exploring the sources of variation in the dataset to expose related variables and provide insight into the biogeochemical processes that control the water chemistry of the system. Factor scores computed from PCA were mapped by date and depth. Patterns observed suggest that (i) fermentation is the process controlling the greatest variability in the dataset and it peaks in May; (ii) iron and sulfate reduction were the dominant terminal electron-accepting processes in the system and were associated with fermentation but had more complex seasonal variability than fermentation; (iii) methanogenesis was also important and associated with bacterial utilization of minerals as a source of electron acceptors (e.g., barite BaSO4); and (iv) seasonal hydrological patterns (wet and dry periods) control the availability of electron acceptors through the reoxidation of reduced iron-sulfur species enhancing iron and sulfate reduction. Copyright ?? 2008 by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America. All rights reserved.

Contamination of ground water, surface water, and soil, and evaluation of selected ground-water pumping alternatives in the Canal Creek area of Aberdeen Proving Ground, Maryland

Science.gov (United States)

Lorah, Michelle M.; Clark, Jeffrey S.

1996-01-01

Chemical manufacturing, munitions filling, and other military-support activities have resulted in the contamination of ground water, surface water, and soil in the Canal Creek area of Aberdeen Proving Ground, Maryland. Chlorinated volatile organic compounds, including 1,1,2,2-tetrachloroethane and trichloroethylene, are widespread ground-water contaminants in two aquifers that are composed of unconsolidated sand and gravel. Distribution and fate of chlorinated organic compounds in the ground water has been affected by the movement and dissolution of solvents in their dense immiscible phase and by microbial degradation under anaerobic conditions. Detection of volatile organic contaminants in adjacent surface water indicates that shallow contaminated ground water discharges to surface water. Semivolatile organic compounds, especially polycyclic aromatic hydrocarbons, are the most prevalent organic contaminants in soils. Various trace elements, such as arsenic, cadmium, lead, and zinc, were found in elevated concentrations in ground water, surface water, and soil. Simulations with a ground-water-flow model and particle tracker postprocessor show that, without remedial pumpage, the contaminants will eventually migrate to Canal Creek and Gunpowder River. Simulations indicate that remedial pumpage of 2.0 million gallons per day from existing wells is needed to capture all particles originating in the contaminant plumes. Simulated pumpage from offsite wells screened in a lower confined aquifer does not affect the flow of contaminated ground water in the Canal Creek area.

Three-dimensional analysis of future groundwater flow conditions and contaminant plume transport in the Hanford Site unconfined aquifer system: FY 1996 and 1997 status report

International Nuclear Information System (INIS)

Cole, C.R.; Wurstner, S.K.; Williams, M.D.; Thorne, P.D.; Bergeron, M.P.

1997-12-01

A three-dimensional numerical model of groundwater flow and transport, based on the Coupled Fluid Energy, and Solute Transport (CFEST) code, was developed for the Hanford Site to support the Hanford Groundwater Project (HGWP), managed by Pacific Northwest National Laboratory. The model was developed to increase the understanding and better forecast the migration of several contaminant plumes being monitored by the HGWP, and to support the Hanford Site Composite Analysis for low-level waste disposal in the 200-Area Plateau. Recent modeling efforts have focused on continued refinement of an initial version of the three-dimensional model developed in 1995 and its application to simulate future transport of selected contaminant plumes in the aquifer system. This version of the model was updated using a more current version of the CFEST code called CFEST96. Prior to conducting simulations of contaminant transport with the three-dimensional model, a previous steady-state, two-dimensional model of the unconfined aquifer system was recalibrated to 1979 water-table conditions with a statistical inverse method implemented in the CFEST-INV computer code. The results of the recalibration were used to refine the three-dimensional conceptual model and to calibrate it with a conceptualization that preserves the two-dimensional hydraulic properties and knowledge of the aquifer's three-dimensional properties for the same 1979 water-table conditions. The transient behavior of the three-dimensional flow model was also calibrated by adjusting model storage properties (specific yield) until transient water-table predictions approximated observed water-table elevations between 1979 and 1996

Attenuation of contaminant plumes in homogeneous aquifers: Sensitivity to source function at moderate to large peclet numbers

International Nuclear Information System (INIS)

Selander, W.N.; Lane, F.E.; Rowat, J.H.

1995-05-01

A groundwater mass transfer calculation is an essential part of the performance assessment for radioactive waste disposal facilities. AECL's IRUS (Intrusion Resistant Underground Structure) facility, which is designed for the near-surface disposal of low-level radioactive waste (LLRW), is to be situated in the sandy overburden at AECL's Chalk River Laboratories. Flow in the sandy aquifers at the proposed IRUS site is relatively homogeneous and advection-dominated (large Peclet numbers). Mass transfer along the mean direction of flow from the IRUS site may be described using the one-dimensional advection-dispersion equation, for which a Green's function representation of downstream radionuclide flux is convenient. This report shows that in advection-dominated aquifers, dispersive attenuation of initial contaminant releases depends principally on two time scales: the source duration and the pulse breakthrough time. Numerical investigation shows further that the maximum downstream flux or concentration depends on these time scales in a simple characteristic way that is minimally sensitive to the shape of the initial source pulse. (author). 11 refs., 2 tabs., 3 figs

Coastal Aquifer Contamination and Geochemical Processes Evaluation in Tugela Catchment, South Africa—Geochemical and Statistical Approaches

Directory of Open Access Journals (Sweden)

Badana Ntanganedzeni

2018-05-01

Full Text Available Assessment of groundwater quality, contamination sources and geochemical processes in the coastal aquifer of Tugela Catchment, South Africa were carried out by the geochemical and statistical approach using major ion chemistry of 36 groundwater samples. Results suggest that the spatial distribution pattern of EC, TDS, Na, Mg, Cl and SO4 are homogenous and elevated concentrations are observed in the wells in the coastal region and few wells near the Tugela River. Wells located far from the coast are enriched by Ca, HCO3 and CO3. Durov diagrams, Gibbs plots, ionic ratios, chloro alkaline indices (CAI1 and CAI2 and correlation analysis imply that groundwater chemistry in the coastal aquifer of Tugela Catchment is regulated by the ion exchange, mineral dissolution, saline sources, and wastewater infiltration from domestic sewage; septic tank leakage and irrigation return flow. Principle component analysis also ensured the role of saline and anthropogenic sources and carbonates dissolution on water chemistry. Spatial distributions of factor score also justify the above predictions. Groundwater suitability assessment indicates that around 80% and 90% of wells exceeded the drinking water standards recommended by the WHO and South African drinking water standards (SAWQG, respectively. Based on SAR, RSC, PI, and MH classifications, most of the wells are suitable for irrigation in the study region. USSL classification suggests that groundwater is suitable for coarse-textured soils and salt-tolerant crops. The study recommends that a proper management plan is required to protect this coastal aquifer efficiently.

Ground-water quality of the surficial aquifer system and the upper Floridan Aquifer, Ocala National Forest and Lake County, Florida, 1990-99

Science.gov (United States)

Adamski, J.C.; Knowles, Leel

2001-01-01

Data from 217 ground-water samples were statistically analyzed to assess the water quality of the surficial aquifer system and Upper Floridan aquifer in the Ocala National Forest and Lake County, Florida. Samples were collected from 49 wells tapping the surficial aquifer system, 141 wells tapping the Upper Floridan aquifer, and from 27 springs that discharge water from the Upper Floridan aquifer. A total of 136 samples was collected by the U.S. Geological Survey from 1995 through 1999. These data were supplemented with 81 samples collected by the St. Johns River Water Management District and Lake County Water Resources Management from 1990 through 1998. In general, the surficial aquifer system has low concentrations of total dissolved solids (median was 41 milligrams per liter) and major ions. Water quality of the surficial aquifer system, however, is not homogeneous throughout the study area. Concentrations of total dissolved solids, many major ions, and nutrients are greater in samples from Lake County outside the Ocala National Forest than in samples from within the Forest. These results indicate that the surficial aquifer system in Lake County outside the Ocala National Forest probably is being affected by agricultural and (or) urban land-use practices. High concentrations of dissolved oxygen (less than 0.1 to 8.2 milligrams per liter) in the surficial aquifer system underlying the Ocala National Forest indicate that the aquifer is readily recharged by precipitation and is susceptible to surface contamination. Concentrations of total dissolved solids were significantly greater in the Upper Floridan aquifer (median was 182 milligrams per liter) than in the surficial aquifer system. In general, water quality of the Upper Floridan aquifer was homogeneous, primarily being a calcium or calciummagnesium- bicarbonate water type. Near the St. Johns River, the water type of the Upper Floridan aquifer is sodium-chloride, corresponding to an increase in total dissolved

An assessment of subsurface contamination of an urban coastal aquifer due to oil spill.

Science.gov (United States)

Nambi, Indumathi M; Rajasekhar, Bokam; Loganathan, Vijay; RaviKrishna, R

2017-04-01

Incidences of leakages of chemicals from underground oil storage tanks or oil-carrying pipelines have posed huge threat to the coastal aquifers around the world. One such leak was recently identified and notified by the people of Tondiarpet, Chennai, India. The assessment of the contamination level was done by obtaining electrical resistivity maps of the subsurface, drilling of 20 new borewells for soil and water analysis, and testing the water quality of 30 existing borewells. Samples were collected from the borewells, and observations were made that included parameters such as odor, moisture, contamination characteristics, lithology, groundwater level, thickness of the free product that are used to demarcate the extent of soil, and water contamination. Furthermore, a multigas detector was used to detect hydrocarbon presence as soil vapor. Moreover, to capture the transport of dissolved hydrocarbons, 10 samples were collected in the periphery of the study area and were analyzed for the presence of petroleum hydrocarbon and polyaromatic hydrocarbon. Analysis of the data indicated the presence of free-phase hydrocarbon in soil and groundwater close to the junction of Thiruvottiyur high (TH) road (TH) and Varadaja Perumal Koil (VPK) street. Although the contaminant plume is confined to a limited area, it has spread more to the southern and eastern side of the pipeline possibly due to continuous abstraction of groundwater by residential apartments. After cutting a trench along the VPK street and plotting of the plume delineation map, observations indicated that the source of the hydrocarbon leak is present in VPK street close to TH road. A multipronged strategy was suggested targeting the remediation of oil in various phases.

Characterisation of the nitrate contamination process in the Seville-Carmona aquifer system; Caracterizacion del proceso de contaminacion por nitratos en el sistema acuifero Sevilla-Carmona

Energy Technology Data Exchange (ETDEWEB)

Gonzalez Vazquez, J.C.; Grande Gil, J.A. [Universidad de Huelva (Spain); Barragan de la Rosa, F.J.; Jimenez Sanchez, J.C. [Universidad de Sevilla (Spain)

1998-07-01

The aim of this work is to characterize the aquifer Sevilla-Carmona by a graphic treatment, in order to determine the environmental problem owing to high concentration of nitrates because of the fact that there are an excessive agricultural fertilization. There is a relationship between the highest nitrate contamination and the crop of the area, mainly cotton and potato. Two factors have been observed to have an influence on this aquifer: excess doses of N- fertilizers and irrigation devices whose excessive water discharge results in leaching of nitrate accumulated in soil and finally toward saturated zone because of rain. (Author) 18 refs.

Coastal aquifers: Scientific advances in the face of global environmental challenges

Science.gov (United States)

Post, Vincent E. A.; Werner, Adrian D.

2017-08-01

Coastal aquifers embody the subsurface transition between terrestrial and marine systems, and form the almost invisible pathway for tremendous volumes of freshwater that flow to the ocean. Changing conditions of the earth's landscapes and oceans can disrupt the fragile natural equilibrium between fresh and saltwater that exists in coastal zones. Among these, over-abstraction of groundwater is considered the leading man-made cause of seawater intrusion. Moreover, many of the world's largest urban settings, where sources of contamination are profuse, have been built over the freshwater in coastal aquifers. Thus, coastal aquifers are important receptors of human impacts to water on Earth (Michael et al., 2017). This Special Issue on 'Investigation and Management of Coastal Aquifers' contains current scientific advances on the topic, dealing with the storage and quality of water, affected by stressors ranging in scale from point source contamination to global climate change.

Three-dimensional geologic modeling and groundwater flow modeling of the Töllinperä aquifer in the Hitura nickel mine area, Finland – providing the framework for restoration and protection of the aquifer

Directory of Open Access Journals (Sweden)

Sami Saraperä

2004-01-01

Full Text Available Elevated concentrations of sulphate, chloride, and nickel were discovered in water samples taken from the Töllinperä aquifer in western Finland. The area is located adjacent to the tailings area of the Hitura nickel mine. Earlier studies revealed that the groundwater contamination resulted from tailings-derived mine waters leaking from a tailings impoundment area. The tailings area directly overlies the Weichselian esker system, part of which is the Töllinperä classified groundwater area. The observed groundwater and surface water contamination resulted in a need to characterize the subsurface geology in the whole area of the contaminated esker aquifer. The primary sedimentary units were introduced into a three-dimensional (3-D geologic model of the aquifer made with EarthVision geologic modeling software. The information obtained from the 3-D geological model was then introduced into a numerical groundwater flow model made with MODFLOW code, which was calibrated with MODFLOWP code.The results of this study were used to guide the sealing of the tailings impoundment in order to prevent the further contamination of the Töllinperä aquifer. The groundwater flow model was used to interpret and simulate the flow system, and to provide a plan to safely continue water supply to local inhabitants from the unpolluted parts of the aquifer.

Determining shallow aquifer vulnerability by the DRASTIC model and hydrochemistry in granitic terrain, southern India

Science.gov (United States)

Mondal, N. C.; Adike, S.; Singh, V. S.; Ahmed, S.; Jayakumar, K. V.

2017-08-01

Shallow aquifer vulnerability has been assessed using GIS-based DRASTIC model by incorporating the major geological and hydrogeological factors that affect and control the groundwater contamination in a granitic terrain. It provides a relative indication of aquifer vulnerability to the contamination. Further, it has been cross-verified with hydrochemical signatures such as total dissolved solids (TDS), Cl-, HCO3-, SO4^{2-} and Cl-/HCO3- molar ratios. The results show four zones of aquifer vulnerability (i.e., negligible, low, moderate and high) based on the variation of DRASTIC Vulnerability Index (DVI) between 39 and 132. About 57% area in the central part is found moderately and highly contaminated due to the 80 functional tannery disposals and is more prone to groundwater aquifer vulnerability. The high range values of TDS (2304-39,100 mg/l); Na+(239- 6,046 mg/l) and Cl- (532-13,652 mg/l) are well correlated with the observed high vulnerable zones. The values of Cl-/HCO3- (molar ratios: 1.4-106.8) in the high vulnerable zone obviously indicate deterioration of the aquifer due to contamination. Further cumulative probability distributions of these parameters indicate several threshold values which are able to demarcate the diverse vulnerability zones in granitic terrain.

Monitoring of emerging contaminants (pharmaceuticals, Personal Care Products, surfactants and heavy metals) in a quaternary detritic aquifer

Science.gov (United States)

Candela, L.; Valdes-Abellan, J.; Jiménez-Martínez, J.

2012-04-01

The presence of 209 emerging compounds, surfactants, priority substances according to the 2008/105/EC Directive, 10 heavy metals and microbiological organisms in blended water and aquifer samples was investigated in a quaternary aquifer. The effects of these compounds over the environment are not clear in many cases, but many of them have been classified as endocrine disruptor compounds, EDC. Their presence in the media is controlled in one hand by their transformation and/or removal rates and, on the other hand, by their continuous release into the media, due to the broad use of these in many human activities (pharmaceuticals, personal care products, pesticides, heavy metals, LAS and others). The attention of this work focusses on the presence and fate of these substances in the vadose zone and the aquifer. The aquifer catchment (81km2) located in SE Spain presents a high natural salinity (with EC values of ~7,500 μS cm-1, and high concentrations of chloride, sulphate and sodium), making it unsuitable to be used as drinking water or irrigation. Two sampling campaigns (February and June 2011) in wells and springs have been carried out top characterize physic-chemical, microbiological and emerging contaminants presence in the aquifer. A total of 209 emerging pollutants grouped into the following classes were analysed: 125 pharmaceutical compounds (Phs), 20 polyaromatic hydrocarbons (PAHs) and Dioxins, 46 pesticides, 3 volatile priority pollutants as well as the most commonly used anionic surfactants were identified for further analysis. Heavy metals included: Cu, Cd, Pb, Hg, Ni, Zn, Sn, Pt, Pd and Tl. Results showed that 39 out of all compounds were detected: 11 pharmaceuticals, 9 PAHs, 19 pesticides, 4 surfactants and 4 heavy metals. Two of the compounds, endosulfan-α and Ni, were detected in concentrations above the allowed regulation. Although results are limited to 2 sampling campaigns, it is important to note that surfactants (LAS), pesticides PAHs and

Understanding Uranium Behavior in a Reduced Aquifer

Science.gov (United States)

Janot, N.; Lezama-Pacheco, J. S.; Williams, K. H.; Bernier-Latmani, R.; Long, P. E.; Davis, J. A.; Fox, P. M.; Yang, L.; Giammar, D.; Cerrato, J. M.; Bargar, J.

2012-12-01

Uranium contamination of groundwater is a concern at several US Department of Energy sites, such Old Rifle, CO. Uranium transport in the environment is mainly controlled by its oxidation state, since oxidized U(VI) is relatively mobile, whereas U(IV) is relatively insoluble. Bio-remediation of contaminated aquifers aims at immobilizing uranium in a reduced form. Previous laboratory and field studies have shown that adding electron donor (lactate, acetate, ethanol) to groundwater stimulates the activity of metal- and sulfate-reducing bacteria, which promotes U(VI) reduction in contaminated aquifers. However, obtaining information on chemical and physical forms of U, Fe and S species for sediments biostimulated in the field, as well as kinetic parameters such as U(VI) reduction rate, is challenging due to the low concentration of uranium in the aquifers (typically bio-remediation experiment at the Old Rifle site, CO, from early iron-reducing conditions to the transition to sulfate-reducing conditions. Several in-well chromatographic columns packed with sediment were deployed and were sampled at different days after the start of bio-reduction. X-ray absorption spectroscopy and X-ray microscopy were used to obtain information on Fe, S and U speciation and distribution. Chemical extractions of the reduced sediments have also been performed, to determine the rate of Fe(II) and U(IV) accumulation.

DNA-SIP identifies sulfate-reducing Clostridia as important toluene degraders in tar-oil-contaminated aquifer sediment

Energy Technology Data Exchange (ETDEWEB)

Winderl, C.; Penning, H.; von Netzer, F.; Meckenstock, R.U.; Lueders, T. [Helmholtz Zentrum Munchen, Neuherberg (Germany)

2010-10-15

Global groundwater resources are constantly challenged by a multitude of contaminants such as aromatic hydrocarbons. Especially in anaerobic habitats, a large diversity of unrecognized microbial populations may be responsible for their degradation. Still, our present understanding of the respective microbiota and their ecophysiology is almost exclusively based on a small number of cultured organisms, mostly within the Proteobacteria. Here, by DNA-based stable isotope probing (SIP), we directly identified the most active sulfate-reducing toluene degraders in a diverse sedimentary microbial community originating from a tar-oil-contaminated aquifer at a former coal gasification plant. On incubation of fresh sediments with {sup 13}C{sub 7}-toluene, the production of both sulfide and (CS{sub 2}){sup 13}CO{sub 2} was clearly coupled to the {sup 13}Clabeling of DNA of microbes related to Desulfosporosinus spp. within the Peptococcaceae (Clostridia). The screening of labeled DNA fractions also suggested a novel benzylsuccinate synthase alpha-subunit (bssA) sequence type previously only detected in the environment to be tentatively affiliated with these degraders. However, carbon flow from the contaminant into degrader DNA was only similar to 50%, pointing toward high ratios of heterotrophic CS{sub 2}-fixation during assimilation of acetyl-CoA originating from the contaminant by these degraders. These findings demonstrate that the importance of non-proteobacterial populations in anaerobic aromatics degradation, as well as their specific ecophysiology in the subsurface may still be largely ungrasped.

Monitoring of the aerobe biodegradation of chlorinated organic solvents by stable isotope analysis

Science.gov (United States)

Horváth, Anikó; Futó, István; Palcsu, László

2014-05-01

Our chemical-biological basic research aims to eliminate chlorinated environmental contaminants from aquifers around industrial areas in the frame of research program supported by the European Social Fund (TÁMOP-4.2.2.A-11/1/KONV-2012-0043). The most careful and simplest way includes the in situ biodegradation with the help of cultured and compound specific strains. Numerous members of Pseudomonas bacteria are famous about function of bioremediation. They can metabolism the environmental hazardous chemicals like gas oils, dyes, and organic solvents. Our research based on the Pseudomonas putida F1 strain, because its ability to degrade halogenated hydrocarbons such as trichloroethylene. Several methods were investigated to estimate the rate of biodegradation, such as the measurement of the concentration of the pollutant along the contamination pathway, the microcosm's studies or the compound specific stable isotope analysis. In this area in the Transcarpathian basin we are pioneers in the stable isotope monitoring of biodegradation. The main goal is to find stable isotope fractionation factors by stable isotope analysis, which can help us to estimate the rate and effectiveness of the biodegradation. The subsequent research period includes the investigation of the method, testing its feasibility and adaptation in the environment. Last but not least, the research gives an opportunity to identify the producer of the contaminant based on the stable isotope composition of the contaminant.

Solvent extraction treatment of PCB contaminated soil at Sparrevohn Long Range Radar Station, Alaska

International Nuclear Information System (INIS)

Weimer, L. D.

1999-01-01

On-site soil treatment at a long range radar station in Alaska, which was contaminated with between 50 and 350 mg/kg of polychlorinated biphenyls (PCBs) is described. The stock-piled soil was treated by the Terra Kleen Response Group, using a solvent extraction process. After the treatment, PCB concentrations in the treated soil were found to have been reduced to less than the target treatment level of 15 mg/kg. Not only was the process successful, it also saved the government about $ 1 million over what hauling and off-site treatment and disposal would have cost. 1 tab

Using Novel Laboratory Incubations and Field Experiments to Identify the Source and Fate of Reactive Organic Carbon in an Arsenic-contaminated Aquifer System

Science.gov (United States)

Stahl, M.; Tarek, M. H.; Badruzzaman, B.; Harvey, C. F.

2017-12-01

Characterizing the sources and fate of organic matter (OM) within aquifer systems is key to our understanding of both the broader global carbon cycle as well as the quality of our groundwater resources. The linkage between the subsurface carbon cycle and groundwater quality is perhaps nowhere more apparent than in the aquifer systems of South and Southeast Asia, where the contamination of groundwater with geogenic arsenic (As) is widespread and threatens the health of millions of individuals. OM fuels the biogeochemical processes driving As mobilization within these aquifers, however the source (i.e., modern surface-derived or aged sedimentary OM) of the reactive OM is widely debated. To characterize the sources of OM driving aquifer redox processes we tracked DIC and DOC concentrations and isotopes (stable and radiocarbon) along groundwater flow-paths and beneath an instrumented study pond at a field site in Bangladesh. We also conducted a set of novel groundwater incubation experiments, where we carbon-dated the DOC at the start and end of a experiment in order to determine the age of the OM that was mineralized. Our carbon/isotope balance reveals that aquifer recharge introduces a large quantity of young (i.e. near modern) OM that is efficiently mineralized within the upper few meters of the aquifer, effectively limiting this pool of reactive surface-sourced OM from being transported deeper into the aquifer where significant As mobilization takes place. The OM mineralized past the upper few meters is an aged, sedimentary source. Consistent with our field data, our incubation experiments show that past the upper few meters of the aquifer the reactive DOC is significantly older than the bulk DOC and has an age consistent with sedimentary OM. Combining our novel set of incubation experiments and a carbon/isotope balance along groundwater flow-paths and beneath our study pond we have identified the sources of reactive OM across different aquifer depths in a

Emerging Water Contaminants: Technical, Legal and Policy Challenges

Science.gov (United States)

Deeb, R. A.; Kresic, N.; Laugier, M. C.; Kavanaugh, M. C.

2002-12-01

Approximately 120 new chemicals are created each year due to ever-improving industry and technology markets. Releases of new contaminants into the environment can occur during production, use and disposal of these chemicals thereby leading to potential contamination of water supply sources. Very few emerging contaminants are regulated. In addition, knowledge gaps regarding emerging contaminants include lack health effects, occurrence (either because these compounds are not measured or because concentrations are below detection limits of readily available analytical techniques) and fate and transport in the environment especially with regards to mobility and persistence. The sources of these compounds are numerous. One source is treated wastewater, which is re-injected into groundwater aquifers for indirect potable reuse purposes. Emerging compounds of concern can be classified in various classes. This presentation will focus on contaminants, which have emerged in the last 10 years including pharmaceuticals (antibiotics/drugs), personal care products (polycyclic musks), pesticides/herbicides, industrial solvents (1,4-dioxane), gasoline additives (MTBE), disinfection byproducts such as NDMA (N-nitrosodimethylamine), and inorganic compounds such as perchlorate and arsenic. This presentation will present technical, legal and legislative challenges posed by the presence of these contaminants in water. Background information including chemical's history of use, sources in the environments, nationwide occurrence, physical and chemical properties, behavior in the environment and technologies for removal from soil and water will be presented. In addition, case studies on MTBE, pharmaceuticals and personal care products, 1,4-dioxane, arsenic and NDMA will be discussed.

Behavioral response to contamination risk information in a spatially explicit groundwater environment: Experimental evidence

Science.gov (United States)

Li, Jingyuan; Michael, Holly A.; Duke, Joshua M.; Messer, Kent D.; Suter, Jordan F.

2014-08-01

This paper assesses the effectiveness of aquifer monitoring information in achieving more sustainable use of a groundwater resource in the absence of management policy. Groundwater user behavior in the face of an irreversible contamination threat is studied by applying methods of experimental economics to scenarios that combine a physics-based, spatially explicit, numerical groundwater model with different representations of information about an aquifer and its risk of contamination. The results suggest that the threat of catastrophic contamination affects pumping decisions: pumping is significantly reduced in experiments where contamination is possible compared to those where pumping cost is the only factor discouraging groundwater use. The level of information about the state of the aquifer also affects extraction behavior. Pumping rates differ when information that synthesizes data on aquifer conditions (a "risk gauge") is provided, despite invariant underlying economic incentives, and this result does not depend on whether the risk information is location-specific or from a whole aquifer perspective. Interestingly, users increase pumping when the risk gauge signals good aquifer status compared to a no-gauge treatment. When the gauge suggests impending contamination, however, pumping declines significantly, resulting in a lower probability of contamination. The study suggests that providing relatively simple aquifer condition guidance derived from monitoring data can lead to more sustainable use of groundwater resources.

Geophysical Signitures From Hydrocarbon Contaminated Aquifers

Science.gov (United States)

Abbas, M.; Jardani, A.

2015-12-01

The task of delineating the contamination plumes as well as studying their impact on the soil and groundwater biogeochemical properties is needed to support the remediation efforts and plans. Geophysical methods including electrical resistivity tomography (ERT), induced polarization (IP), ground penetrating radar (GPR), and self-potential (SP) have been previously used to characterize contaminant plumes and investigate their impact on soil and groundwater properties (Atekwana et al., 2002, 2004; Benson et al., 1997; Campbell et al., 1996; Cassidy et al., 2001; Revil et al., 2003; Werkema et al., 2000). Our objective was to: estimate the hydrocarbon contamination extent in a contaminated site in northern France, and to adverse the effects of the oil spill on the groundwater properties. We aim to find a good combination of non-intrusive and low cost methods which we can use to follow the bio-remediation process, which is planned to proceed next year. We used four geophysical methods including electrical resistivity tomography, IP, GPR, and SP. The geophysical data was compared to geochemical ones obtained from 30 boreholes installed in the site during the geophysical surveys. Our results have shown: low electrical resistivity values; high chargeability values; negative SP anomalies; and attenuated GPR reflections coincident with groundwater contamination. Laboratory and field geochemical measurements have demonstrated increased groundwater electrical conductivity and increased microbial activity associated with hydrocarbon contamination of groundwater. Our study results support the conductive model suggested by studies such as Sauck (2000) and Atekwana et al., (2004), who suggest that biological alterations of hydrocarbon contamination can substantially modify the chemical and physical properties of the subsurface, producing a dramatic shift in the geo-electrical signature from resistive to conductive. The next stage of the research will include time lapse borehole

Combining lead isotopes and cluster analysis to distinguish the Guarani and Serra Geral Aquifer Systems and contaminated waters in a highly industrialized area in Southern Brazil.

Science.gov (United States)

Kuhn, Isadora Aumond; Roisenberg, Ari

2017-10-01

The Rio dos Sinos Watershed area is located at the Middle-West region of the Rio Grande do Sul State, Southern Brazil, along thirty two municipalities and affecting 1.5 million inhabitants and many important industrial centers. Three main aquifers are recognized in the study area: the unconfined-fractured Serra Geral Aquifer System, the porous Guarani Aquifer System, and the Permian Aquitard. This study aims to understand groundwater, surface water and human activity interactions in the Rio dos Sinos Watershed, evaluating the application of stable lead isotopic ratios analyzed for this propose. Thirty six groundwater samples, 8 surface water samples and 5 liquid effluents of tanneries and landfills samples were measured using a Thermal Ionization Mass Spectrometer Thermo-Finnigan and a Neptune Multi-Collector Inductively Coupled Plasma Mass Spectrometer. Groundwater isotopic ratios have a wider range compared to the surface water, with less radiogenic averages 208 Pb/ 204 Pb = 38.1837 vs 38.4050 (standard deviation = 0.2921 vs 0.1343) and 206 Pb/ 204 Pb = 18.2947 vs 18.4766 (standard deviation = 0.2215 vs 0.1059), respectively. Industrial liquid effluents (tanneries and industrial landfill) have averages 208 Pb/ 204 Pb = 38.1956 and 206 Pb/ 204 Pb = 18.3169, distinct from effluent samples of domestic sanitary landfill (averages 208 Pb/ 204 Pb = 38.2353 and 206 Pb/ 204 Pb = 18.6607). Hierarchical cluster analysis led to distinguish six groups of groundwater, representing the three aquifers that occur in the area, two clusters suggesting groundwater mixtures and one demonstrating a highly contaminated groundwater. By analyzing the cluster results and wells' stratigraphic profiles it was possible to distinguish the different aquifers in the area. The Serra Geral Aquifer System has 206 Pb/ 204 Pb ratios between 18.4718 and 18.7089; 207 Pb/ 204 Pb between 15.6692 and 15.6777; 208 Pb/ 204 Pb between 38.6826 and 38.7616; 207 Pb/ 206 Pb between 0.8372 and 0

Dual Pump Recovery (DPR System to Extract Freshwater in Coastal Aquifers

Directory of Open Access Journals (Sweden)

C. Otto

2002-06-01

Full Text Available The paper describes the hydraulic theory of recovering a dense plume using a newly devised dual pump recover system (DPR and its feasibility to half the remediation time of a contaminated unconfined aquifer in a coastal urban environment. Although the DPR system was successfully applied to clean up the polluted aquifer, the hydraulic principles and techniques are also applicable to extract fresh groundwater from coastal aquifers without the risk of saltwater incursion.

Decontamination method and device for radiation contaminated product

International Nuclear Information System (INIS)

Morikawa, Kenji; Ohinata, Hiroshi; Omata, Kazuo; Sato, Toshihiko; Nakajima, Yoshihiko; Ichikawa, Seigo.

1996-01-01

In the present invention, radiation contaminated products generated during shot peening are decontaminated by a chelating agent, and the chelating agent is removed from the radiation contaminated products. Then the temperature of the radiation contaminated products is elevated by hot blowing at a temperature higher than a boiling point of the solvent. Then, a solvent is added to the radiation contaminated products and the solvent is evaporated abruptly. The solution of the chelating agent remained while being deposited thereto is removed by evaporation to remove it from the radiation contaminated products together with the solvent. With such procedures, all of the decontamination steps can be completed in one device without requiring a large space or not moving the radiation contaminated products on every step. (T.M.)

Attenuation of landfill leachate by UK Triassic sandstone aquifer materials. 1. Fate of inorganic pollutants in laboratory columns

Science.gov (United States)

Thornton, Steven F.; Tellam, John H.; Lerner, David N.

2000-05-01

The attenuation of inorganic contaminants in acetogenic and methanogenic landfill leachate by calcareous and carbonate-deficient, oxide-rich Triassic sandstone aquifer materials from the English Midlands was examined in laboratory columns. Aqueous equilibrium speciation modelling, simple transport modelling and chemical mass balance approaches are used to evaluate the key processes and aquifer geochemical properties controlling contaminant fate. The results indicate that leachate-rock interactions are dominated by ion-exchange processes, acid-base and redox reactions and sorption/precipitation of metal species. Leachate NH 4 is attenuated by cation exchange with the aquifer sediments; however, NH 4 migration could be described with a simple model using retardation factors. Organic acids in the acetogenic leachate buffered the system pH at low levels during flushing of the calcareous aquifer material. In contrast, equilibrium with Al oxyhydroxide phases initially buffered pH (˜4.5) during flushing of the carbonate-deficient sandstone with methanogenic leachate. This led to the mobilisation of sorbed and oxide-bound heavy metals from the aquifer sediment which migrated as a concentrated pulse at the leachate front. Abiotic reductive dissolution of Mn oxyhydroxides on each aquifer material by leachate Fe 2+ maintains high concentrations of dissolved Mn and buffers the leachate inorganic redox system. This feature is analogous to the Mn-reducing zones found in leachate plumes and in the experiments provides a sink for the leachate Fe load and other heavy metals. The availability of reactive solid phase Mn oxyhydroxides limits the duration of redox buffering and Fe attenuation by these aquifer sediments. Aquifer pH and redox buffering capacity exert a fundamental influence on leachate inorganic contaminant fate in these systems. The implications for the assessment of aquifer vulnerability at landfills are discussed and simple measurements of aquifer properties which

Quantitation of buried contamination by use of solvents. [degradation of silicone polymers by amine solvents

Science.gov (United States)

Pappas, S. P.; Hsiao, Y. C.; Hill, L. W.

1973-01-01

Spore recovery form cured silicone potting compounds using amine solvents to degrade the cured polymers was investigated. A complete list of solvents and a description of the effect of each on two different silicone polymers is provided.

Nonhazardous solvent composition and method for cleaning metal surfaces

International Nuclear Information System (INIS)

Googin, J.M.; Simandl, R.F.; Thompson, L.M.

1993-01-01

A solvent composition for displacing greasy and oily contaminants as well as water and/or aqueous residue from metallic surfaces, especially surfaces of radioactive materials so that such surfaces can be wiped clean of the displaced contaminants, water and/or aqueous residue. The solvent composition consists essentially of a blend of nonpolar aliphatic hydrocarbon solvent having a minimum flash point of about 140 F and 2 to 25 volume percent of a polar solvent having a flash point sufficiently high so as to provide the solvent composition with a minimum flash point of at least 140 F. The solvent composition is nonhazardous so that when it is used to clean the surfaces of radioactive materials the waste in the form of paper or cloth wipes, lab coats and the like used in the cleaning operation is not considered to be mixed waste composed of a hazardous solvent and a radioactive material

Intensive exploitation of a karst aquifer leads to Cryptosporidium water supply contamination.

Science.gov (United States)

Khaldi, S; Ratajczak, M; Gargala, G; Fournier, M; Berthe, T; Favennec, L; Dupont, J P

2011-04-01

Groundwater from karst aquifers is an important source of drinking water worldwide. Outbreaks of cryptosporidiosis linked to surface water and treated public water are regularly reported. Cryptosporidium oocysts are resistant to conventional drinking water disinfectants and are a major concern for the water industry. Here, we examined conditions associated with oocyst transport along a karstic hydrosystem, and the impact of intensive exploitation on Cryptosporidium oocyst contamination of the water supply. We studied a well-characterized karstic hydrosystem composed of a sinkhole, a spring and a wellbore. Thirty-six surface water and groundwater samples were analyzed for suspended particulate matter, turbidity, electrical conductivity, and Cryptosporidium and Giardia (oo)cyst concentrations. (Oo)cysts were identified and counted by means of solid-phase cytometry (ChemScan RDI(®)), a highly sensitive method. Cryptosporidium oocysts were detected in 78% of both surface water and groundwater samples, while Giardia cysts were found in respectively 22% and 8% of surface water and groundwater samples. Mean Cryptosporidium oocyst concentrations were 29, 13 and 4/100 L at the sinkhole, spring and wellbore, respectively. Cryptosporidium oocysts were transported from the sinkhole to the spring and the wellbore, with respective release rates of 45% and 14%, suggesting that oocysts are subject to storage and remobilization in karst conduits. Principal components analysis showed that Cryptosporidium oocyst concentrations depended on variations in hydrological forcing factors. All water samples collected during intensive exploitation contained oocysts. Control of Cryptosporidium oocyst contamination during intensive exploitation is therefore necessary to ensure drinking water quality. Copyright © 2011. Published by Elsevier Ltd.

Assessment of natural attenuation of ground-water contamination at sites FT03, LF13, and WP14/LF15, Dover Air Force Base, Delaware

Science.gov (United States)

Barbaro, Jeffrey R.

2002-01-01

Water-quality, aquifer-sediment, and hydro-logic data were used to assess the effectiveness of natural attenuation of ground-water contamination at Fire Training Area Three, the Rubble Area Landfill, the Liquid Waste Disposal Landfill, and the Receiver Station Landfill in the East Management Unit of Dover Air Force Base, Delaware. These sites, which are contaminated with chlorinated solvents and fuel hydrocarbons, are under-going long-term monitoring to determine if natural attenuation continues to sufficiently reduce contaminant concentrations to meet regulatory requirements. This report is the first assessment of the effectiveness of natural attenuation at these sites since long-term monitoring began in 1999, and follows a preliminary investigation done in 1995?96. This assessment was done by the U.S. Geological Survey in cooperation with the U.S. Air Force.Since 1995?96, additional information has been collected and used in the current assessment. The conclusions in this report are based primarily on ground-water samples collected from January through March 2000. Previous analytical results from selected wells, available geologic and geo-physical well logs, and newly acquired information such as sediment organic-carbon measurements, hydraulic-conductivity measurements determined from slug tests on wells in the natural attenuation study area, and water-level measurements from surficial-aquifer wells also were used in this assessment. This information was used to: (1) calculate retardation factors and estimate contaminant migration velocities, (2) improve estimates of ground-water flow directions and inferred contaminant migration pathways, (3) better define the areal extent of contamination and the proximity of contaminants to discharge areas and the Base boundary, (4) develop a better under-standing of the vertical variability of contaminant concentrations and redox conditions, (5) evaluate the effects of temporal changes on concentrations in the plumes and

Full scale solvent extraction remedial results

International Nuclear Information System (INIS)

Cash, A.B.

1992-01-01

Sevenson Extraction Technology, Inc. has completed the development of the Soil Restoration Unit (initially developed by Terra-Kleen Corporation), a mobile, totally enclosed solvent extraction treatment facility for the removal of organic contaminated media is greater by a closed loop, counter current process that recycles all solvents. The solvents used are selected for the individual site dependant upon the contaminants, such as PCB's, oil, etc. and the soil conditions. A mixture of up to fourteen non-toxic solvents can be used for complicated sites. The full scale unit has been used to treat one superfund site, the Traband Site in Tulsa, Oklahoma, and is currently treating another superfund site, the Pinette's Salvage Yard Site in Washburn, Maine. The full scale Soil Restoration Unit has also been used at a non-superfund site, as part of a TSCA Research and Development permit. The results from these sites will be discussed in brief herein, and in more detail in the full paper

The effect of vadose zone heterogeneities on vapor phase migration and aquifer contamination by volatile organics

Energy Technology Data Exchange (ETDEWEB)

Seneviratne, A.; Findikakis, A.N. [Bechtel Corporation, San Francisco, CA (United States)

1995-03-01

Organic vapors migrating through the vadose zone and inter-phase transfer can contribute to the contamination of larger portions of aquifers than estimated by accounting only for dissolved phase transport through the saturated zone. Proper understanding of vapor phase migration pathways is important for the characterization of the extent of both vadose zone and the saturated zone contamination. The multiphase simulation code T2VOC is used to numerically investigate the effect of heterogeneties on the vapor phase migration of chlorobenzene at a hypothetical site where a vapor extraction system is used to remove contaminants. Different stratigraphies consisting of alternate layers of high and low permeability materials with soil properties representative of gravel, sandy silt and clays are evaluated. The effect of the extent and continuity of low permeability zones on vapor migration is evaluated. Numerical simulations are carried out for different soil properties and different boundary conditions. T2VOC simulations with zones of higher permeability were made to assess the role of how such zones in providing enhanced migration pathways for organic vapors. Similarly, the effect of the degree of saturation of the porous medium on vapor migration was for a range of saturation values. Increased saturation reduces the pore volume of the medium available for vapor diffusion. Stratigraphic units with higher aqueous saturation can retard the vapor phase migration significantly.

Groundwater recharge and agricultural contamination

Science.gov (United States)

Böhlke, J.K.

2002-01-01

Agriculture has had direct and indirect effects on the rates and compositions of groundwater recharge and aquifer biogeochemistry. Direct effects include dissolution and transport of excess quantities of fertilizers and associated materials and hydrologic alterations related to irrigation and drainage. Some indirect effects include changes in water–rock reactions in soils and aquifers caused by increased concentrations of dissolved oxidants, protons, and major ions. Agricultural activities have directly or indirectly affected the concentrations of a large number of inorganic chemicals in groundwater, for example NO3–, N2, Cl, SO42–, H+, P, C, K, Mg, Ca, Sr, Ba, Ra, and As, as well as a wide variety of pesticides and other organic compounds. For reactive contaminants like NO3–, a combination of chemical, isotopic, and environmental-tracer analytical approaches might be required to resolve changing inputs from subsequent alterations as causes of concentration gradients in groundwater. Groundwater records derived from multi-component hydrostratigraphic data can be used to quantify recharge rates and residence times of water and dissolved contaminants, document past variations in recharging contaminant loads, and identify natural contaminant-remediation processes. These data indicate that many of the world's surficial aquifers contain transient records of changing agricultural contamination from the last half of the 20th century. The transient agricultural groundwater signal has important implications for long-term trends and spatial heterogeneity in discharge.

Aquifer Vulnerability Investigation Using Geoelectric Method in Parts ...

African Journals Online (AJOL)

The generated longitudinal conductance map showed poor protective capacity ... capacity makes the aquifer in the study area vulnerable to contamination ..... Sedimentation and Structure of the Niger Delta. ... Direct application of the Dar.

Preliminary hydrogeologic assessment of a ground-water contamination area in Wolcott, Connecticut

Science.gov (United States)

Stone, J.R.; Casey, G.D.; Mondazzi, R.A.; Frick, T.W.

1997-01-01

Contamination of ground water by volatile organic compounds and inorganic constituents has been identified at a number of industrial sites in the Town of Wolcott, Connecticut. Contamination is also present at a municipal landfill in the City of Waterbury that is upgradient from the industrial sites in the local ground-water-flow system. The study area, which lies in the Western Highlands of Connecticut, is in the Mad River Valley, a tributary to the Naugatuck River. Geohydrologic units (aquifer materials) include unconsolidated glacial sediments (surficial materials) and fractured crystalline (metamorphic) bedrock. Surficial materials include glacial till, coarse-grained andfine-grained glacial stratified deposits, and postglacial floodplain alluvium and swamp deposits. The ground-water-flow system in the surficial aquifer is complex because the hydraulic properties of the surficial materials are highly variable. In the bedrock aquifer, ground water moves exclusively through fractures. Hydrologic characteristics of the crystalline bedrock-degree of confinement, hydraulic conductivity, storativity, and porosity-are poorly defined in the study area. Further study is needed to adequately assess ground-water flow and contaminant migration under current or past hydrologic conditions. All known water-supply wells in the study area obtain water from the bedrock aquifer. Twenty households in a hillside residential area on Tosun Road currently obtain drinking water from private wells tapping the bedrock aquifer. The extent of contamination in the bedrock aquifer and the potential for future contamination from known sources of contamination in the surficial aquifer is of concern to regulatory agencies. Previous investigations have identified ground-water contamination by volatile organic compounds at the Nutmeg Valley Road site area. Contamination has been associated with on-site disposal of heavy metals, chlorinated and non-chlorinated volatile organic compounds, and

Hydrogeochemical and mineralogical effects of sustained CO₂ contamination in a shallow sandy aquifer: A field-scale controlled release experiment

DEFF Research Database (Denmark)

Cahill, Aaron Graham; Marker, Pernille Aabye; Jakobsen, Rasmus

2014-01-01

A shallow aquifer CO2 contamination experiment was performed to investigate evolution of water chemistry and sediment alteration following leakage from geological storage by physically simulating a leak from a hypothetical storage site. In a carbonate-free aquifer, in western Denmark, a total...... of 1600 kg of gas phase CO2 was injected at 5 and 10 m depth over 72 days through four inclined injection wells into aeolian and glacial sands. Water chemistry was monitored for pH, EC, and dissolved element evolution through an extensive network of multilevel sampling points over 305 days. Sediment cores...... were taken pre and postinjection and analyzed to search for effects on mineralogy and sediment properties. Results showed the simulated leak to evolve in two distinct phases; an advective elevated ion pulse followed by increasing persistent acidification. Spatial and temporal differences in evolution...

Steam Injection For Soil And Aquifer Remediation

Science.gov (United States)

The purpose of this Issue Paper is to provide to those involved in assessing remediation technologies for specific sites basic technical information on the use of steam injection for the remediation of soils and aquifers that are contaminated by...

Evaluation of ethyl lactate as solvent in Fenton oxidation for the remediation of total petroleum hydrocarbon (TPH)-contaminated soil.

Science.gov (United States)

Jalilian Ahmadkalaei, Seyedeh Pegah; Gan, Suyin; Ng, Hoon Kiat; Abdul Talib, Suhaimi

2017-07-01

Due to the health and environmental risks posed by the presence of petroleum-contaminated areas around the world, remediation of petroleum-contaminated soil has drawn much attention from researchers. Combining Fenton reaction with a solvent has been proposed as a novel way to remediate contaminated soils. In this study, a green solvent, ethyl lactate (EL), has been used in conjunction with Fenton's reagents for the remediation of diesel-contaminated soil. The main aim of this research is to determine how the addition of EL affects Fenton reaction for the destruction of total petroleum hydrocarbons (TPHs) within the diesel range. Specifically, the effects of different parameters, including liquid phase volume-to-soil weight (L/S) ratio, hydrogen peroxide (H 2 O 2 ) concentration and EL% on the removal efficiency, have been studied in batch experiments. The results showed that an increase in H 2 O 2 resulted in an increase in removal efficiency of TPH from 68.41% at H 2 O 2  = 0.1 M to 90.21% at H 2 O 2  = 2 M. The lowest L/S, i.e. L/S = 1, had the highest TPH removal efficiency of 85.77%. An increase in EL% up to 10% increased the removal efficiency to 96.74% for TPH, and with further increase in EL%, the removal efficiency of TPH decreased to 89.6%. EL with an optimum value of 10% was found to be best for TPH removal in EL-based Fenton reaction. The power law and pseudo-first order equations fitted well to the experimental kinetic data of Fenton reactions.

Method of removing contaminants from plastic resins

Science.gov (United States)

Bohnert, George W.; Hand, Thomas E.; DeLaurentiis, Gary M.

2008-11-18

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Method for removing contaminants from plastic resin

Science.gov (United States)

Bohnert, George W.; Hand, Thomas E.; DeLaurentiis, Gary M.

2008-12-30

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Surfactant-enhanced aquifer remediation at the Portsmouth Gaseous Diffusion Plant

International Nuclear Information System (INIS)

Jackson, R.E.; Londergan, J.T.; Pickens, J.

1995-01-01

Many DOE facilities are situated in areas of sand and gravel which have become polluted with dense, non-aqueous phase liquids or DNAPLs, such as chlorinated solvents, from the various industrial operations at these facilities. The presence of such DNAPLs in sand and gravel aquifers is now recognized as the principal factor in the failure of standard ground-water remediation methods, i.e., open-quotes pump-and-treatclose quotes operations, to decontaminate such systems. The principal objective of this study is to demonstrate that multi-component DNAPLs can be readily solubilized in sand and gravel aquifers by dilute surfactant solutions

Solvent recycle/contaminant reduction testing - Phase I, Task 3. Topical progress report, June 1994--December 1994

International Nuclear Information System (INIS)

1995-07-01

The Department of Energy (DOE) is now faced with the task of meeting decontamination and decommissioning obligations at numerous facilities by the year 2019. Due to the tremendous volume of material involved, innovative decontamination technologies are being sought that can reduce the volumes of contaminated waste materials and secondary wastes requiring disposal. With sufficient decontamination, some of the material from DOE facilities could be released as scrap into the commercial sector for recycle, thereby reducing the volume of radioactive waste requiring disposal. Although recycling may initially prove to be more costly than current disposal practices, rapidly increasing disposal costs are expected to make recycling more and more cost effective. Additionally, recycling is now perceived as the ethical choice in a world where the consequences of replacing resources and throwing away reusable materials are impacting the well-being of the environment. This report describes the solvent recyle test program for EDTA/ammonium carbonate solvent

Guidelines for active spreading during in situ chemical oxidation to remediate contaminated groundwater

Science.gov (United States)

The effectiveness of in situ chemical oxidation to remediate contaminated aquifers depends on the extent and duration of contact between the injected treatment chemical and the groundwater contaminant (the reactants). Techniques that inject and extract in the aquifer to ‘ac...

Response and recovery of a pristine groundwater ecosystem impacted by toluene contamination - A meso-scale indoor aquifer experiment

Science.gov (United States)

Herzyk, Agnieszka; Fillinger, Lucas; Larentis, Michael; Qiu, Shiran; Maloszewski, Piotr; Hünniger, Marko; Schmidt, Susanne I.; Stumpp, Christine; Marozava, Sviatlana; Knappett, Peter S. K.; Elsner, Martin; Meckenstock, Rainer; Lueders, Tillmann; Griebler, Christian

2017-12-01

Microbial communities are the driving force behind the degradation of contaminants like aromatic hydrocarbons in groundwater ecosystems. However, little is known about the response of native microbial communities to contamination in pristine environments as well as their potential to recover from a contamination event. Here, we used an indoor aquifer mesocosm filled with sandy quaternary calciferous sediment that was continuously fed with pristine groundwater to study the response, resistance and resilience of microbial communities to toluene contamination over a period of almost two years, comprising 132 days of toluene exposure followed by nearly 600 days of recovery. We observed an unexpectedly high intrinsic potential for toluene degradation, starting within the first two weeks after the first exposure. The contamination led to a shift from oxic to anoxic, primarily nitrate-reducing conditions as well as marked cell growth inside the contaminant plume. Depth-resolved community fingerprinting revealed a low resistance of the native microbial community to the perturbation induced by the exposure to toluene. Distinct populations that were dominated by a small number of operational taxonomic units (OTUs) rapidly emerged inside the plume and at the plume fringes, partially replacing the original community. During the recovery period physico-chemical conditions were restored to the pristine state within about 35 days, whereas the recovery of the biological parameters was much slower and the community composition inside the former plume area had not recovered to the original state by the end of the experiment. These results demonstrate the low resilience of sediment-associated groundwater microbial communities to organic pollution and underline that recovery of groundwater ecosystems cannot be assessed solely by physico-chemical parameters.

Influence of soil and hydrocarbon properties on the solvent extraction of high-concentration weathered petroleum from contaminated soils.

Science.gov (United States)

Sui, Hong; Hua, Zhengtao; Li, Xingang; Li, Hong; Wu, Guozhong

2014-05-01

Petroleum ether was used to extract petroleum hydrocarbons from soils collected from six oil fields with different history of exploratory and contamination. It was capable of fast removing 76-94 % of the total petroleum hydrocarbons including 25 alkanes (C11-C35) and 16 US EPA priority polycyclic aromatic hydrocarbons from soils at room temperature. The partial least squares analysis indicated that the solvent extraction efficiencies were positively correlated with soil organic matter, cation exchange capacity, moisture, pH, and sand content of soils, while negative effects were observed in the properties reflecting the molecular size (e.g., molecular weight and number of carbon atoms) and hydrophobicity (e.g., water solubility, octanol-water partition coefficient, soil organic carbon partition coefficient) of hydrocarbons. The high concentration of weathered crude oil at the order of 10(5) mg kg(-1) in this study was demonstrated adverse for solvent extraction by providing an obvious nonaqueous phase liquid phase for hydrocarbon sinking and increasing the sequestration of soluble hydrocarbons in the insoluble oil fractions during weathering. A full picture of the mass distribution and transport mechanism of petroleum contaminants in soils will ultimately require a variety of studies to gain insights into the dynamic interactions between environmental indicator hydrocarbons and their host oil matrix.

System for removing contaminants from plastic resin

Science.gov (United States)

Bohnert, George W.; Hand, Thomas E.; DeLaurentiis, Gary M.

2010-11-23

A resin recycling system that produces essentially contaminant-free synthetic resin material in an environmentally safe and economical manner. The system includes receiving the resin in container form. A grinder grinds the containers into resin particles. The particles are exposed to a solvent in one or more solvent wash vessels, the solvent contacting the resin particles and substantially removing contaminants on the resin particles. A separator is used to separate the resin particles and the solvent. The resin particles are then placed in solvent removing element where they are exposed to a solvent removing agent which removes any residual solvent remaining on the resin particles after separation.

Artificial Intelligence-Based Models for the Optimal and Sustainable Use of Groundwater in Coastal Aquifers

Science.gov (United States)

Sreekanth, J.; Datta, Bithin

2011-07-01

Overexploitation of the coastal aquifers results in saltwater intrusion. Once saltwater intrusion occurs, it involves huge cost and long-term remediation measures to remediate these contaminated aquifers. Hence, it is important to have strategies for the sustainable use of coastal aquifers. This study develops a methodology for the optimal management of saltwater intrusion prone aquifers. A linked simulation-optimization-based management strategy is developed. The methodology uses genetic-programming-based models for simulating the aquifer processes, which is then linked to a multi-objective genetic algorithm to obtain optimal management strategies in terms of groundwater extraction from potential well locations in the aquifer.

Correlative Cryo-Tem Cryo-Stxm and Cryo-Shxm Investigation of Selenium Bioreduction in a Contaminated Aquifer

Science.gov (United States)

Fakra, S.; Luef, B.; Tyliszczak, T.; Castelle, C. J.; Mullin, S. W.; Hug, L. A.; Williams, K. H.; Marcus, M.; Banfield, J. F.

2015-12-01

Accurate mapping of the composition and ultrastructure of minerals and cells is key to understanding biogeochemical process in contaminated environments. Here we developed two apparatus that allow correlation of cryogenic transmission electron microscopy (TEM), synchrotron hard X-ray microprobe (SHXM) and scanning transmission X-ray microscopy (STXM) datasets. These cryogenic methods enabled precise determination of the distribution, valence state and structure of selenium in intact biofilms sampled during a biostimulation experiment in a contaminated aquifer near Rifle, CO, USA. Results were replicated in the laboratory via anaerobic selenate-reducing enrichment cultures. 16S rRNA analyses of field-derived biofilm indicated the dominance of Betaproteobacteria from the Comamonadaceae family, and uncultivated members of the Simplicispira genus. The major product in field and culture-derived biofilms consists of ~25-300 nm red amorphous Se0 aggregates of colloidal nanoparticles. Correlative analyses of the cultures provided direct evidence for microbial dissimilatory reduction of Se(VI) to Se(IV) to Se0. X-ray diffraction and Se K-edge extended X-ray absorption fine structure spectroscopy revealed red amorphous Se0 with a first shell Se-Se interatomic distance of 2.339 ± 0.003 Å. STXM showed that these aggregates are strongly associated with a protein-rich biofilm matrix containing acidic polysaccharides. From Rifle groundwater, we isolated a strain that shares 98.9% 16S rRNA gene sequence identity with Dechloromonas aromatica RCB and grows anaerobically by oxidizing acetate and reducing selenate. We refer to this isolate as Dechloromonas selenatis strain RGW99. 3D cryo-electron tomography showed that Se0 particles do not form inside the cytoplasm but rather originate in the cell membrane. The end product of selenate reduction by D. selenatis is 240 ± 66 nm diameter red amorphous Se0 colloidal aggregates. This product was found to be stable for months. Overall

Groundwater quality of the Gulf Coast aquifer system, Houston, Texas, 2010

Science.gov (United States)

Oden, Jeannette H.; Brown, Dexter W.; Oden, Timothy D.

2011-01-01

During March–December 2010, the U.S. Geological Survey, in cooperation with the city of Houston, collected source-water samples from 60 municipal supply wells in the Houston area. These data were collected as part of an ongoing study to determine concentrations, spatial extent, and associated geochemical conditions that might be conducive for mobility and transport of selected naturally occurring contaminants (selected trace elements and radionuclides) in the Gulf Coast aquifer system in the Houston area. In the summers of 2007 and 2008, a reconnaissance-level survey of these constituents in untreated water from 28 municipal supply wells was completed in the Houston area. Included in this report are the complete analytical results for 47 of the 60 samples collected in 2010—those results which were received from the laboratories and reviewed by the authors as of December 31, 2010. All of the wells sampled were screened in the Gulf Coast aquifer system; 22 were screened entirely in the Evangeline aquifer, and the remaining 25 wells contained screened intervals that intersected both Evangeline and Chicot aquifers. The data documented in this report were collected as part of an ongoing study to characterize source-water-quality conditions in untreated groundwater prior to drinking-water treatment. An evaluation of contaminant occurrence in source water provides background information regarding the presence of a contaminant in the environment. Because source-water samples were collected prior to any treatment or blending that potentially could alter contaminant concentrations, the water-quality results documented by this report represent the quality of the source water, not the quality of finished drinking water provided to the public.

Groundwater vulnerability assessment in karstic aquifers using COP method.

Science.gov (United States)

Bagherzadeh, Somayeh; Kalantari, Nasrollah; Nobandegani, Amir Fadaei; Derakhshan, Zahra; Conti, Gea Oliveri; Ferrante, Margherita; Malekahmadi, Roya

2018-05-02

Access to safe and reliable drinking water is amongst the important indicators of development in each society, and water scarcity is one of the challenges and limitations affecting development at national and regional levels and social life and economic activity areas. Generally, there are two types of drinking water sources: the first type is surface waters, including lakes, rivers, and streams and the second type is groundwaters existing in aquifers. Amongst aquifers, karst aquifers play an important role in supplying water sources of the world. Therefore, protecting these aquifers from pollution sources is of paramount importance. COP method is amongst the methods to investigate the intrinsic vulnerability of this type of aquifers, so that areas susceptible to contamination can be determined before being contaminated and these sources can be protected. In the present study, COP method was employed in order to spot the regions that are prone to contamination in the region. This method uses the properties of overlying geological layers above the water table (O factor), the concentration of flow (C factor), and precipitation (P factor) over the aquifer, as the parameters to assess the intrinsic vulnerability of groundwater resources. In this regard, geographical information system (GIS) and remote sensing (RS) were utilized to prepare the mentioned factors and the intrinsic vulnerability map was obtained. The results of COP method indicated that the northwest and the west of the region are highly and very vulnerable. This study indicated that regions with low vulnerability were observed in eastern areas, which accounted for 15.6% of the area. Moderate vulnerability was 40% and related to the northeast and southeast of the area. High vulnerability was 38.2% and related to western and southwestern regions. Very high vulnerability was 6.2% and related to the northwest of the area. By means of the analysis of sensitivity of the model, it was determined that the focus

Fate of sulfamethoxazole, 4-nonylphenol, and 17beta-estradiol in groundwater contaminated by wastewater treatment plant effluent.

Science.gov (United States)

Barber, Larry B; Keefe, Steffanie H; Leblanc, Denis R; Bradley, Paul M; Chapelle, Francis H; Meyer, Michael T; Loftin, Keith A; Kolpin, Dana W; Rubio, Fernando

2009-07-01

Organic wastewater contaminants (OWCs) were measured in samples collected from monitoring wells located along a 4.5-km transect of a plume of groundwater contaminated by 60 years of continuous rapid infiltration disposal of wastewater treatment plant effluent. Fifteen percent of the 212 OWCs analyzed were detected, including the antibiotic sulfamethoxazole (SX), the nonionic surfactant degradation product 4-nonylphenol (NP), the solvent tetrachloroethene (PCE), and the disinfectant 1,4-dichlorobenzene (DCB). Comparison of the 2005 sampling results to data collected from the same wells in 1985 indicates that PCE and DCB are transported more rapidly in the aquiferthan NP, consistent with predictions based on compound hydrophobicity. Natural gradient in situ tracer experiments were conducted to evaluate the subsurface behavior of SX, NP, and the female sex hormone 17beta-estradiol (E2) in two oxic zones in the aquifer: (1) a downgradient transition zone at the interface between the contamination plume and the overlying uncontaminated groundwater and (2) a contaminated zone located beneath the infiltration beds, which have not been loaded for 10 years. In both zones, breakthrough curves for the conservative tracer bromide (Br-) and SX were nearly coincident, whereas NP and E2 were retarded relative to Br- and showed mass loss. Retardation was greater in the contaminated zone than in the transition zone. Attenuation of NP and E2 in the aquifer was attributed to biotransformation, and oxic laboratory microcosm experiments using sediments from the transition and contaminated zones show that uniform-ring-labeled 14C 4-normal-NP was biodegraded more rapidly 130-60% recovered as 14CO2 in 13 days) than 4-14C E2 (20-90% recovered as 14CO2 in 54 days). There was little difference in mineralization potential between sites.

Arsenic pollution of groundwater in Vietnam exacerbated by deep aquifer exploitation for more than a century

Science.gov (United States)

Winkel, Lenny H. E.; Trang, Pham Thi Kim; Lan, Vi Mai; Stengel, Caroline; Amini, Manouchehr; Ha, Nguyen Thi; Viet, Pham Hung; Berg, Michael

2011-01-01

Arsenic contamination of shallow groundwater is among the biggest health threats in the developing world. Targeting uncontaminated deep aquifers is a popular mitigation option although its long-term impact remains unknown. Here we present the alarming results of a large-scale groundwater survey covering the entire Red River Delta and a unique probability model based on three-dimensional Quaternary geology. Our unprecedented dataset reveals that ∼7 million delta inhabitants use groundwater contaminated with toxic elements, including manganese, selenium, and barium. Depth-resolved probabilities and arsenic concentrations indicate drawdown of arsenic-enriched waters from Holocene aquifers to naturally uncontaminated Pleistocene aquifers as a result of > 100 years of groundwater abstraction. Vertical arsenic migration induced by large-scale pumping from deep aquifers has been discussed to occur elsewhere, but has never been shown to occur at the scale seen here. The present situation in the Red River Delta is a warning for other As-affected regions where groundwater is extensively pumped from uncontaminated aquifers underlying high arsenic aquifers or zones. PMID:21245347

Characterization of arsenic-contaminated aquifer sediments from eastern Croatia by ion microbeam, PIXE and ICP-OES techniques

Energy Technology Data Exchange (ETDEWEB)

Ujević Bošnjak, M., E-mail: magdalena.ujevic@hzjz.hr [Croatian National Institute of Public Health, Rockefelerova 7, 10000 Zagreb (Croatia); Fazinić, S. [Institute Ruđer Bošković, Bijenička cesta, 10000 Zagreb (Croatia); Duić, Ž. [University of Zagreb, Faculty of Mining, Geology and Petroleum Engineering, Pierottijeva 6, Zagreb (Croatia)

2013-10-01

Highlights: •ICP-OES and PIXE used in the characterization of As-contaminated sediments. •Observed high correlations between the results obtained by those techniques. •Discrepancies observed for Mn, and for the highest As concentrations. •Microbeam analyses showed As association with sulphides and iron. -- Abstract: Groundwater arsenic contamination has been evidenced in eastern Croatia and hydrochemical results suggest that the occurrence of arsenic in the groundwater depends on the local geology, hydrogeology, and geochemical characteristics of the aquifer. In order to perform the sediment characterization and to investigate arsenic association with the other elements in the sediments, 10 samples from two boreholes (PVc-3 and Gundinci 1) in eastern Croatia were analyzed using two techniques: PIXE (without sample pre-treatment) and ICP-OES (after digestion), as well by ion microbeam analyses. The results of the PIXE and ICP-OES techniques showed quite good agreement; however, greater discrepancies were observed at the higher arsenic and manganese mass ratios. According to both techniques, higher As mass ratios were observed in the sediments from the PVc-3 core (up to 651 mg/kg and 491 mg/kg using PIXE and ICP-OES analyses respectively) than from the Gundinci 1 core (up to 60 mg/kg using both techniques). Although arsenic association with Fe is expected, no correlation was observed. The microbeam analyses demonstrated that arsenic is associated with sulphides and iron in the most As-contaminated sample from the PVc-3 core, while this relationship was not evident in the most As-contaminated sample from the Gundinci 1 borehole.

Characterization of arsenic-contaminated aquifer sediments from eastern Croatia by ion microbeam, PIXE and ICP-OES techniques

International Nuclear Information System (INIS)

Ujević Bošnjak, M.; Fazinić, S.; Duić, Ž.

2013-01-01

Highlights: •ICP-OES and PIXE used in the characterization of As-contaminated sediments. •Observed high correlations between the results obtained by those techniques. •Discrepancies observed for Mn, and for the highest As concentrations. •Microbeam analyses showed As association with sulphides and iron. -- Abstract: Groundwater arsenic contamination has been evidenced in eastern Croatia and hydrochemical results suggest that the occurrence of arsenic in the groundwater depends on the local geology, hydrogeology, and geochemical characteristics of the aquifer. In order to perform the sediment characterization and to investigate arsenic association with the other elements in the sediments, 10 samples from two boreholes (PVc-3 and Gundinci 1) in eastern Croatia were analyzed using two techniques: PIXE (without sample pre-treatment) and ICP-OES (after digestion), as well by ion microbeam analyses. The results of the PIXE and ICP-OES techniques showed quite good agreement; however, greater discrepancies were observed at the higher arsenic and manganese mass ratios. According to both techniques, higher As mass ratios were observed in the sediments from the PVc-3 core (up to 651 mg/kg and 491 mg/kg using PIXE and ICP-OES analyses respectively) than from the Gundinci 1 core (up to 60 mg/kg using both techniques). Although arsenic association with Fe is expected, no correlation was observed. The microbeam analyses demonstrated that arsenic is associated with sulphides and iron in the most As-contaminated sample from the PVc-3 core, while this relationship was not evident in the most As-contaminated sample from the Gundinci 1 borehole

Aquifer Testing And Rebound Study In Support Of The 100-H Deep Chromium Investigation

International Nuclear Information System (INIS)

Smoot, J.L.

2010-01-01

The 100-HR-3 Groundwater Operable Unit (OU) second Comprehensive Environmental Response, Compensation, and Liability Act of 1980 (CERCLA) 5-year review (DOEIRL-2006-20, The Second CERCLA Five-Year Review Report for the Hanford Site) set a milestone to conduct an investigation of deep hexavalent chromium contamination in the sediments of the Ringold upper mud (RUM) unit, which underlies the unconfined aquifer in the 100-H Area. The 5-year review noted that groundwater samples from one deep well extending below the aquitard (i.e., RUM) exceeded both the groundwater standard of 48 parts per billion (ppb) (Ecology Publication 94-06, Model Toxics Control Act Cleanup Statute and Regulation) and the federal drinking water standard of 100 μg/L for hexavalent chromium. The extent of hexavalent chromium contamination in this zone is not well understood. Action 12-1 from the 5-year review is to perform additional characterization of the aquifer below the initial aquitard. Field characterization and aquifer testing were performed in the Hanford Site's 100-H Area to address this milestone. The aquifer tests were conducted to gather data to answer several fundamental questions regarding the presence of the hexavalent chromium in the deep sediments of the RUM and to determine the extent and magnitude of deeper contamination. The pumping tests were performed in accordance with the Description of Work for Aquifer Testing in Support of the 100-H Deep Chromium Investigation (SGW-41302). The specific objectives for the series of tests were as follows: (1) Evaluate the sustainable production of the subject wells using step-drawdown and constant-rate pumping tests. (2) Collect water-level data to evaluate the degree of hydraulic connection between the RUM and the unconfined (upper) aquifer (natural or induced along the well casing). (3) Evaluate the hydraulic properties of a confined permeable layer within the RUM.; (4) Collect time-series groundwater samples during testing to evaluate

Polyhydroxyalkanoate as a slow-release carbon source for in situ bioremediation of contaminated aquifers: From laboratory investigation to pilot-scale testing in the field.

Science.gov (United States)

Pierro, Lucia; Matturro, Bruna; Rossetti, Simona; Sagliaschi, Marco; Sucato, Salvatore; Alesi, Eduard; Bartsch, Ernst; Arjmand, Firoozeh; Papini, Marco Petrangeli

2017-07-25

A pilot-scale study aiming to evaluate the potential use of poly-3-hydroxy-butyrate (PHB) as an electron donor source for in situ bioremediation of chlorinated hydrocarbons in groundwater was conducted. Compared with commercially available electron donors, PHB offers a restricted fermentation pathway (i.e., through acetic acid and molecular hydrogen) by avoiding the formation of any residual carbon that could potentially spoil groundwater quality. The pilot study was carried out at an industrial site in Italy, heavily contaminated by different chlorinated aliphatic hydrocarbons (CAHs). Prior to field testing, PHB was experimentally verified as a suitable electron donor for biological reductive dechlorination processes at the investigated site by microcosm studies carried out on site aquifer material and measuring the quantitative transformation of detected CAHs to ethene. Owing to the complex geological characteristics of the aquifer, the use of a groundwater circulation well (GCW) was identified as a potential strategy to enable effective delivery and distribution of electron donors in less permeable layers and to mobilise contaminants. A 3-screened, 30-m-deep GCW coupled with an external treatment unit was installed at the site. The effect of PHB fermentation products on the in situ reductive dechlorination processes were evaluated by quantitative real-time polymerase chain reaction (qPCR). The results from the first 4 months of operation clearly demonstrated that the PHB fermentation products were effectively delivered to the aquifer and positively influenced the biological dechlorination activity. Indeed, an increased abundance of Dehalococcoides mccartyi (up to 6.6 fold) and reduced CAH concentrations at the installed monitoring wells were observed. Copyright © 2016 Elsevier B.V. All rights reserved.

Ground-water contamination and legal controls in Michigan

Science.gov (United States)

Deutsch, Morris

1963-01-01

The great importance of the fresh ground-water resources of Michigan is evident because 90 percent of the rural and about 70 percent of the total population of the State exclusive of the Detroit metropolitan area are supplied from underground sources. The water-supply and public-health problems that have been caused by some cases of ground-water contamination in the State illustrate the necessity of protecting this vital resource.Manmade and natural contaminants, including many types of chemical and organic matter, have entered many of the numerous aquifers of the State. Aquifers have been contaminated by waste-laden liquids percolating from the surface or from the zone of aeration and by direct injection to the aquifer itself. Industrial and domestic wastes, septic tanks, leaking sewers, flood waters or other poor quality surface waters, mine waters, solids stored or spread at the surface, and even airborne wastes all have been sources of ground-water contamination in Michigan. In addition, naturally occurring saline waters have been induced into other aquifers by overpumping or unrestricted flow from artesian wells, possibly by dewatering operations, and by the deepening of surface stream channels. Vertical migration of saline waters through open holes from formations underlying various important aquifers also has spoiled some of the fresh ground waters in the State. In spite of the contamination that has occurred, however, the total amount of ground water that has been spoiled is only a small part of the total resource. Neither is the contamination so widespread as that of the surface streams of Michigan.Overall legal authority to control most types of ground-water contamination in the State has been assigned by the Michigan Legislature to the Water Resources Commission, although the Department of Conservation and the Health Department also exercise important water-pollution control functions. The Michigan Supreme Court, in an important case upholding the power

Distribution of aquifers, liquid-waste impoundments, and municipal water-supply sources, Massachusetts

Science.gov (United States)

Delaney, David F.; Maevsky, Anthony

1980-01-01

Impoundments of liquid waste are potential sources of ground-water contamination in Massachusetts. The map report, at a scale of 1 inch equals 4 miles, shows the idstribution of aquifers and the locations of municipal water-supply sources and known liquid-waste impoundments. Ground water, an important source of municipal water supply, is produced from shallow sand and gravel aquifers that are generally unconfined, less than 200 feet thick, and yield less than 2,000 gallons per minute to individual wells. These aquifers commonly occupy lowlands and stream valleys and are most extensive in eastern Massachusetts. Surface impoundments of liquid waste are commonly located over these aquifers. These impoundments may leak and allow waste to infiltrate underlying aquifers and alter their water quality. (USGS)

Hydrogeology and ground-water flow of the drift and Platteville aquifer system, St Louis Park, Minnesota

Science.gov (United States)

Lindgren, R.J.

1995-01-01

Three aquifers and two confining units have been delineated within the drift underlying the area near the site of a former coal-tar distillation and wood-preserving plant in St. Louis Park, Minnesota. The hydrogeologic units of the drift, in descending order, are the upper drift aquifer, the upper drift confining unit, the middle drift aquifer, the lower drift confining unit. and the lower drift aquifer. A contamination plume consisting of coal-tar derivatives exists in the drift aquifers and in the Platteville aquifer underlying the southern part of the plant site and areas to the south and east of the plant site.

Integration of models of various types of aquifers for water quality management in the transboundary area of the Soča/Isonzo river basin (Slovenia/Italy).

Science.gov (United States)

Vižintin, Goran; Ravbar, Nataša; Janež, Jože; Koren, Eva; Janež, Naško; Zini, Luca; Treu, Francesco; Petrič, Metka

2018-04-01

Due to intrinsic characteristics of aquifers groundwater frequently passes between various types of aquifers without hindrance. The complex connection of underground water paths enables flow regardless of administrative boundaries. This can cause problems in water resources management. Numerical modelling is an important tool for the understanding, interpretation and management of aquifers. Useful and reliable methods of numerical modelling differ with regard to the type of aquifer, but their connections in a single hydrodynamic model are rare. The purpose of this study was to connect different models into an integrated system that enables determination of water travel time from the point of contamination to water sources. The worst-case scenario is considered. The system was applied in the Soča/Isonzo basin, a transboundary river in Slovenia and Italy, where there is a complex contact of karst and intergranular aquifers and surface flows over bedrock with low permeability. Time cell models were first elaborated separately for individual hydrogeological units. These were the result of numerical hydrological modelling (intergranular aquifer and surface flow) or complex GIS analysis taking into account the vulnerability map and tracer tests results (karst aquifer). The obtained cellular models present the basis of a contamination early-warning system, since it allows an estimation when contaminants can be expected to appear, and in which water sources. The system proves that the contaminants spread rapidly through karst aquifers and via surface flows, and more slowly through intergranular aquifers. For this reason, karst water sources are more at risk from one-off contamination incidents, while water sources in intergranular aquifers are more at risk in cases of long-term contamination. The system that has been developed is the basis for a single system of protection, action and quality monitoring in the areas of complex aquifer systems within or on the borders of

Tools for Management of Chlorinated Solvent - Contaminated Sites

Science.gov (United States)

2009-12-03

Movie Lee Ann Doner – (2008) MS CSU “Sandy aquifers” Image from Fred Payne /ARCADIS New Paradigm After NRC 2005 l~r SERDP. Advancing solvent plume...Situ Bioremediation Using Emulsified  Edible  Oil”   AFCEE (http://www.afcee.brooks.af.mil/products/techtrans/) - “Principles and Practices of Enhanced...Anaerobic Bioremediation of  Chlorinated Solvents”  - “Protocol for In Situ Bioremediation of Chlorinated Solvents Using  Edible  Oil” 232 Short Course

Hydrogeology of the Susquehanna River valley-fill aquifer system in the Endicott-Vestal area of southwestern Broome County, New York

Science.gov (United States)

Randall, Allan D.; Kappel, William M.

2015-07-29

The village of Endicott, New York, and the adjacent town of Vestal have historically used groundwater from the Susquehanna River valley-fill aquifer system for municipal water supply, but parts of some aquifers in this urban area suffer from legacy contamination from varied sources. Endicott would like to identify sites distant from known contamination where productive aquifers could supply municipal wells with water that would not require intensive treatment. The distribution or geometry of aquifers within the Susquehanna River valley fill in western Endicott and northwestern Vestal are delineated in this report largely on the basis of abundant borehole data that have been compiled in a table of well records.

In situ bioreduction of technetium and uranium in a nitrate-contaminated aquifer

International Nuclear Information System (INIS)

IstokD, Jonathan; Senko, J.M.; Krumholz, Lee R.; Watson, David B.; Bogle, Mary Anna; Peacock, Aaron D.; Change, Y.J.; White, David C.

2004-01-01

The potential to stimulate an indigenous microbial community to reduce a mixture of U(VI) and Tc(VII) in the presence of high (120 mM) initial NO 3 - co-contamination was evaluated in a shallow unconfined aquifer using a series of single-well, push-pull tests. In the absence of added electron donor, NO 3 - , Tc(VII), and U(VI) reduction was not detectable. However, in the presence of added ethanol, glucose, or acetate to serve as electron donor, rapid NO 3 - utilization was observed. The accumulation of NO 2 - , the absence of detectable NH 4 + accumulation, and the production of N 2 O during in situ acetylene-block experiments suggest that NO 3 - was being consumed via denitrification. Tc(VII) reduction occurred concurrently with NO 3 - reduction, but U(VI) reduction was not observed until two or more donor additions resulted in iron-reducing conditions, as detected by the production of Fe(II). Reoxidation/remobilization of U(IV) was also observed in tests conducted with high (120 mM) but not low (1 mM) initial NO 3 - concentrations and not during acetylene-block experiments conducted with high initial NO 3 - . These results suggest that NO 3 - -dependent microbial U(IV) oxidation may inhibit or reverse U(VI) reduction and decrease the stability of U(IV) in this environment. Changes in viable biomass, community composition, metabolic status, and respiratory state of organisms harvested from down-well microbial samplers deployed during these tests were consistent with the conclusions that electron donor additions resulted in microbial growth, the creation of anaerobic conditions, and an increase in activity of metal-reducing organisms (e.g., Geobacter). The results demonstrate that it is possible to stimulate the simultaneous bioreduction of U(VI) and Tc(VII) mixtures commonly found with NO 3 - co-contamination at radioactive waste sites.

Biogeochemistry at a wetland sediment-alluvial aquifer interface in a landfill leachate plume

Science.gov (United States)

Lorah, M.M.; Cozzarelli, I.M.; Böhlke, J.K.

2009-01-01

The biogeochemistry at the interface between sediments in a seasonally ponded wetland (slough) and an alluvial aquifer contaminated with landfill leachate was investigated to evaluate factors that can effect natural attenuation of landfill leachate contaminants in areas of groundwater/surface-water interaction. The biogeochemistry at the wetland-alluvial aquifer interface differed greatly between dry and wet conditions. During dry conditions (low water table), vertically upward discharge was focused at the center of the slough from the fringe of a landfill-derived ammonium plume in the underlying aquifer, resulting in transport of relatively low concentrations of ammonium to the slough sediments with dilution and dispersion as the primary attenuation mechanism. In contrast, during wet conditions (high water table), leachate-contaminated groundwater discharged upward near the upgradient slough bank, where ammonium concentrations in the aquifer where high. Relatively high concentrations of ammonium and other leachate constituents also were transported laterally through the slough porewater to the downgradient bank in wet conditions. Concentrations of the leachate-associated constituents chloride, ammonium, non-volatile dissolved organic carbon, alkalinity, and ferrous iron more than doubled in the slough porewater on the upgradient bank during wet conditions. Chloride, non-volatile dissolved organic carbon (DOC), and bicarbonate acted conservatively during lateral transport in the aquifer and slough porewater, whereas ammonium and potassium were strongly attenuated. Nitrogen isotope variations in ammonium and the distribution of ammonium compared to other cations indicated that sorption was the primary attenuation mechanism for ammonium during lateral transport in the aquifer and the slough porewater. Ammonium attenuation was less efficient, however, in the slough porewater than in the aquifer and possibly occurred by a different sorption mechanism. A

A Greedy Approach for Placement of Subsurface Aquifer Wells in an Ensemble Filtering Framework

KAUST Repository

El Gharamti, Mohamad; Marzouk, Youssef M.; Huan, Xun; Hoteit, Ibrahim

2015-01-01

Optimizing wells placement may help in better understanding subsurface solute transport and detecting contaminant plumes. In this work, we use the ensemble Kalman filter (EnKF) as a data assimilation tool and propose a greedy observational design algorithm to optimally select aquifer wells locations for updating the prior contaminant ensemble. The algorithm is greedy in the sense that it operates sequentially, without taking into account expected future gains. The selection criteria is based on maximizing the information gain that the EnKF carries during the update of the prior uncertainties. We test the efficiency of this algorithm in a synthetic aquifer system where a contaminant plume is set to migrate over a 30 years period across a heterogenous domain.

A Greedy Approach for Placement of Subsurface Aquifer Wells in an Ensemble Filtering Framework

KAUST Repository

El Gharamti, Mohamad

2015-11-26

Optimizing wells placement may help in better understanding subsurface solute transport and detecting contaminant plumes. In this work, we use the ensemble Kalman filter (EnKF) as a data assimilation tool and propose a greedy observational design algorithm to optimally select aquifer wells locations for updating the prior contaminant ensemble. The algorithm is greedy in the sense that it operates sequentially, without taking into account expected future gains. The selection criteria is based on maximizing the information gain that the EnKF carries during the update of the prior uncertainties. We test the efficiency of this algorithm in a synthetic aquifer system where a contaminant plume is set to migrate over a 30 years period across a heterogenous domain.

Uranium series geochemistry in aquifers: quantification of transport mechanisms of uranium and daughter products: the chalk aquifer (Champagne, France)

International Nuclear Information System (INIS)

Hubert, A.

2005-09-01

With the increase of contaminant flux of radionuclides in surface environment (soil, river, aquifer...), there is a need to understand and model the processes that control the distribution of uranium and its daughter products during transport within aquifers. We have used U-series disequilibria as an analogue for the transport of uranium and its daughter products in aquifer to understand such mechanisms. The measurements of uranium ( 234 U et 238 U), thorium ( 230 Th et 232 Th), 226 Ra and 222 Rn isotopes in the solid and liquid phases of the chalk aquifer in Champagne (East of France) allows us to understand the processes responsible for fractionation within the uranium decay chain. Fractionations are induced by physical and chemical properties of the elements (leaching, adsorption) but also by radioactive properties (recoil effect during α-decay). For the first time a comprehensive sampling of the solid phase has been performed, allowing quantifying mechanisms responsible for the long term evolution of the aquifer. A non steady state 1D model has been developed which takes into account leaching, adsorption processes as well as radioactive filiation and α-recoil effect. Retardation coefficients have been calculated for uranium, thorium and radium. The aquifer is characterised by a double porosity, and the contribution of fracture and matrix porosity on the water/rock interaction processes has been estimated. (author)

Apparatus and method for removing solvent from carbon dioxide in resin recycling system

Science.gov (United States)

Bohnert, George W [Harrisonville, MO; Hand, Thomas E [Lee's Summit, MO; DeLaurentiis, Gary M [Jamestown, CA

2009-01-06

A two-step resin recycling system and method solvent that produces essentially contaminant-free synthetic resin material. The system and method includes one or more solvent wash vessels to expose resin particles to a solvent, the solvent contacting the resin particles in the one or more solvent wash vessels to substantially remove contaminants on the resin particles. A separator is provided to separate the solvent from the resin particles after removal from the one or more solvent wash vessels. The resin particles are next exposed to carbon dioxide in a closed loop carbon dioxide system. The closed loop system includes a carbon dioxide vessel where the carbon dioxide is exposed to the resin, substantially removing any residual solvent remaining on the resin particles after separation. A separation vessel is also provided to separate the solvent from the solvent laden carbon dioxide. Both the carbon dioxide and the solvent are reused after separation in the separation vessel.

Combining stable isotopes with contamination indicators: A method for improved investigation of nitrate sources and dynamics in aquifers with mixed nitrogen inputs.

Science.gov (United States)

Minet, E P; Goodhue, R; Meier-Augenstein, W; Kalin, R M; Fenton, O; Richards, K G; Coxon, C E

2017-11-01

Excessive nitrate (NO 3 - ) concentration in groundwater raises health and environmental issues that must be addressed by all European Union (EU) member states under the Nitrates Directive and the Water Framework Directive. The identification of NO 3 - sources is critical to efficiently control or reverse NO 3 - contamination that affects many aquifers. In that respect, the use of stable isotope ratios 15 N/ 14 N and 18 O/ 16 O in NO 3 - (expressed as δ 15 N-NO 3 - and δ 18 O-NO 3 - , respectively) has long shown its value. However, limitations exist in complex environments where multiple nitrogen (N) sources coexist. This two-year study explores a method for improved NO 3 - source investigation in a shallow unconfined aquifer with mixed N inputs and a long established NO 3 - problem. In this tillage-dominated area of free-draining soil and subsoil, suspected NO 3 - sources were diffuse applications of artificial fertiliser and organic point sources (septic tanks and farmyards). Bearing in mind that artificial diffuse sources were ubiquitous, groundwater samples were first classified according to a combination of two indicators relevant of point source contamination: presence/absence of organic point sources (i.e. septic tank and/or farmyard) near sampling wells and exceedance/non-exceedance of a contamination threshold value for sodium (Na + ) in groundwater. This classification identified three contamination groups: agricultural diffuse source but no point source (D+P-), agricultural diffuse and point source (D+P+) and agricultural diffuse but point source occurrence ambiguous (D+P±). Thereafter δ 15 N-NO 3 - and δ 18 O-NO 3 - data were superimposed on the classification. As δ 15 N-NO 3 - was plotted against δ 18 O-NO 3 - , comparisons were made between the different contamination groups. Overall, both δ variables were significantly and positively correlated (p contamination groups revealed that denitrification did not occur in the absence of point

Aquifer recharging in South Carolina: radiocarbon in environmental hydrogeology

International Nuclear Information System (INIS)

Stone, P.A.; Knox, R.L.; Mathews, T.D.

1985-01-01

Radiocarbon activities of dissolved inorganic carbon (and tritium activities where infiltration rates are rapid and aquifers shallow) provide relatively unambiguous and inexpensive evidence for identification of significant recharge areas. Such evidence is for the actual occurrence of modern recharge in the aquifer and thus is less inferential than stratigraphic or potentiometric evidence. These underutilized isotopic techniques are neither arcane nor complex and have been more-or-less standardized by earlier researchers. In South Carolina, isotopic evidence has been used from both calcareous and siliceous sedimentary aquifers and fractured crystalline rock aquifers. The Tertiary limestone aquifer is shown not to be principally recharged in its subcrop area, unlike conditions assumed for many other sedimentary aquifers in southeastern United States, and instead receives considerable lateral recharge from interfingering updip Tertiary sand aquifers in the middle coastal plain. Induced recharging at Hilton Head Island is mixing ancient relict water and modern recharge water. Recharging to deeper portions of the Cretaceous Middendorf basal sand aquifer occurs at least as far coastward as the middle coastal plain, near sampling sites that stratigraphically appear to be confined. Pronounced mineralization of water in fractured rocks cannot be considered as evidence of ancient or relict ground water that is isolated from modern contaminants, some of these waters contain considerable radiocarbon and hydrogen-bomb tritium

Ultrasonic aqueous cleaning as a replacement for chlorinated solvent cleaning

International Nuclear Information System (INIS)

Thompson, L.M.; Simandl, R.F.

1992-01-01

The Oak Ridge Y-12 Plant has been involved in the replacement of chlorinated solvents since 1982. One of the most successful replacement efforts has been the substitution of vapor degreasers or soak tanks using chlorinated solvents with ultrasonic cleaning using aqueous detergents. Recently, funding was obtained from the Department of Energy Office (DOE) of Technology Development to demonstrate this technology. A unit has been procured and installed in the vacuum pump shop area to replace the use of a solvent soak tank. Initially, the solvents used in the shop were CFC-113 and a commercial brand cleaner which contained both perchloroethylene and methylene chloride. While the ultrasonic unit was being procured, a terpene-based solvent was used. Generally, parts were soaked overnight in order to soften baked-on vanish. Many times, wire brushing was used to help remove remaining contamination. Initial testing with the ultrasonic cleaner indicated cleaning times of 20 min were as effective as the overnight solvent soaks in removing contamination. Wire brushing was also not required following the ultrasonic cleaning as was sometimes required with the solvent soak

Hydrogeologic controls on ground-water and contaminant discharge to the Columbia River near the Hanford Townsite

International Nuclear Information System (INIS)

Luttrell, S.P.; Newcomer, D.R.; Teel, S.S.; Vermeul, V.R.

1992-11-01

The purpose of this study is to quantify ground-water and contaminant discharge to the Columbia River in the Hanford Townsite vicinity. The primary objectives of the work are to: describe the hydrogeologic setting and controls on ground-water movement and contaminant discharge to the Columbia River; understand the river/aquifer relationship and its effects on contaminant discharge to the Columbia River; quantify the ground-water and contaminant mass discharge to the Columbia River; and provide data that may be useful for a three-dimensional model of ground-water flow and contaminant transport in the Hanford Townsite study area. The majority of ground-water contamination occurs within the unconfined aquifer; therefore, ground-water and contaminant discharge from the unconfined aquifer is the emphasis of this study. The period of study is primarily from June 1990 through March 1992

An overview of nitrate sources and operating processes in arid and semiarid aquifer systems.

Science.gov (United States)

Gutiérrez, Mélida; Biagioni, Richard N; Alarcón-Herrera, Maria Teresa; Rivas-Lucero, Bertha A

2018-05-15

Nitrate concentration in most aquifers in arid and semi-arid areas has increased in the past several decades as a result of human activities. Under the predominantly oxic conditions of these aquifers, denitrification is inhibited, allowing nitrate, a soluble and stable form of nitrogen (N), to accumulate. Because of its close association with municipal and agricultural wastes, nitrate is commonly used as an indicator of anthropogenic contamination. Aquifers affected by agricultural waste may contain salts from irrigation returns and herbicides in addition to nitrates. Preventing leakage from soil to deeper parts of the aquifer is thus a priority in the sustainable management of aquifers in arid and semiarid areas. Studies report a wide range of nitrate concentrations distributed non-uniformly within the aquifer, with roughly 40% and 20% of sampled wells exceeding 50mg/L nitrate in shallow and deep parts of the aquifer respectively. In aquifers at risk of becoming contaminated, nitrate isotopes (δ 15 N, δ 18 O, Δ 17 O) can be used to identify the source of nitrogen as mineral or organic fertilizer, sewage, or atmospheric deposition. A variety of mathematical models (crop, hydrological, geochemical, or a combination of them) have been successful in identifying best practices that minimize N leakage without negatively affecting crop yield. In addition, field research in crop management, e.g., conservation agriculture, has yielded promising results in determining the adequate dosage and time of application of fertilizers to reduce N losses. Examples of key dryland aquifers impacted by nitrate are discussed, and some of the most pressing challenges to achieve sustainability are presented. Copyright © 2017 Elsevier B.V. All rights reserved.

A stable isotope approach for source apportionment of chlorinated ethene plumes at a complex multi-contamination events urban site

Science.gov (United States)

Nijenhuis, Ivonne; Schmidt, Marie; Pellegatti, Eleonora; Paramatti, Enrico; Richnow, Hans Hermann; Gargini, Alessandro

2013-10-01

The stable carbon isotope composition of chlorinated aliphatic compounds such as chlorinated methanes, ethanes and ethenes was examined as an intrinsic fingerprint for apportionment of sources. A complex field site located in Ferrara (Italy), with more than 50 years history of use of chlorinated aliphatic compounds, was investigated in order to assess contamination sources. Several contamination plumes were found in a complex alluvial sandy multi-aquifer system close to the river Po; sources are represented by uncontained former industrial and municipal dump sites as well as by spills at industrial areas. The carbon stable isotope signature allowed distinguishing 2 major sources of contaminants. One source of chlorinated aliphatic contaminants was strongly depleted in 13C (-40‰ which is commonly observed in recent production of chlorinated solvents. The degradation processes in the plumes could be traced interpreting the isotope enrichment and depletion of parent and daughter compounds, respectively. We demonstrate that, under specific production conditions, namely when highly chlorinated ethenes are produced as by-product during chloromethanes production, 13C depleted fingerprinting of contaminants can be obtained and this can be used to track sources and address the responsible party of the pollution in urban areas.

In-Situ Anaerobic Biosurfactant Production Process For Remediation Of DNAPL Contamination In Subsurface Aquifers

Science.gov (United States)

Albino, J. D.; Nambi, I. M.

2009-12-01

Microbial Enhanced Oil Recovery (MEOR) and remediation of aquifers contaminated with hydrophobic contaminants require insitu production of biosurfactants for mobilization of entrapped hydrophobic liquids. Most of the biosurfactant producing microorganisms produce them under aerobic condition and hence surfactant production is limited in subsurface condition due to lack of oxygen. Currently bioremediation involves expensive air sparging or excavation followed by exsitu biodegradation. Use of microorganisms which can produce biosurfactants under anaerobic conditions can cost effectively expedite the process of insitu bioremediation or mobilization. In this work, the feasibility of anaerobic biosurfactant production in three mixed anaerobic cultures prepared from groundwater and soil contaminated with chlorinated compounds and municipal sewage sludge was investigated. The cultures were previously enriched under complete anaerobic conditions in the presence of Tetrachloroethylene (PCE) for more than a year before they were studied for biosurfactant production. Biosurfactant production under anaerobic conditions was simulated using two methods: i) induction of starvation in the microbial cultures and ii) addition of complex fermentable substrates. Positive result for biosurfactant production was not observed when the cultures were induced with starvation by adding PCE as blobs which served as the only terminal electron acceptor. However, slight reduction in interfacial tension was noticed which was caused by the adherence of microbes to water-PCE interface. Biosurfactant production was observed in all the three cultures when they were fed with complex fermentable substrates and surface tension of the liquid medium was lowered below 35 mN/m. Among the fermentable substrates tested, vegetable oil yielded highest amount of biosurfactant in all the cultures. Complete biodegradation of PCE to ethylene at a faster rate was also observed when vegetable oil was amended to the

Vulnerability of deep groundwater in the Bengal Aquifer System to contamination by arsenic

Science.gov (United States)

Burgess, W.G.; Hoque, M.A.; Michael, H.A.; Voss, C.I.; Breit, G.N.; Ahmed, K.M.

2010-01-01

Shallow groundwater, the primary water source in the Bengal Basin, contains up to 100 times the World Health Organization (WHO) drinking-water guideline of 10g l 1 arsenic (As), threatening the health of 70 million people. Groundwater from a depth greater than 150m, which almost uniformly meets the WHO guideline, has become the preferred alternative source. The vulnerability of deep wells to contamination by As is governed by the geometry of induced groundwater flow paths and the geochemical conditions encountered between the shallow and deep regions of the aquifer. Stratification of flow separates deep groundwater from shallow sources of As in some areas. Oxidized sediments also protect deep groundwater through the ability of ferric oxyhydroxides to adsorb As. Basin-scale groundwater flow modelling suggests that, over large regions, deep hand-pumped wells for domestic supply may be secure against As invasion for hundreds of years. By contrast, widespread deep irrigation pumping might effectively eliminate deep groundwater as an As-free resource within decades. Finer-scale models, incorporating spatial heterogeneity, are needed to investigate the security of deep municipal abstraction at specific urban locations. ?? 2010 Macmillan Publishers Limited. All rights reserved.

Benzoate-driven dehalogenation of chlorinated ethenes in microbial cultures from a contaminated aquifer

Energy Technology Data Exchange (ETDEWEB)

Bunge, M.; Kleikemper, J.; Miniaci, C.; Duc, L.; Muusse, M.G.; Zeyer, J. [Swiss Federal Institute of Technology (ETH), Zurich (Switzerland). Inst. of Biogeochemistry and Pollutant Dynamics, Soil Biology; Hause, G. [Halle-Wittenberg Univ., Halle (Germany). Biocenter

2007-10-15

Microbial dehalogenation of tetrachloroethene (PCE) and cis-dichloroethene (cis-DCE) was studied in cultures from a continuous stirred tank reactor initially inoculated with aquifer material from a PCE-contaminated site. Cultures amended with hydrogen and acetate readily dechlorinated PCE and cis-DCE; however, this transformation was incomplete and resulted in the accumulation of chlorinated intermediates and only small amounts of ethene within 60 days of incubation. Conversely, microbial PCE and cis-DCE dechlorination in cultures with benzoate and acetate resulted in the complete transformation to ethene within 30 days. Community fingerprinting by denaturing gradient gel electrophoresis (DGGE) revealed the predominance of phylotypes closely affiliated with Desulfitobacterium, Dehalococcoides, and Syntrophus species. The Dehalococcoides culture VZ, obtained from small whitish colonies in cis-DCE dechlorinating agarose cultures, revealed an irregular cell diameter between 200 and 500 nm, and a spherical or biconcave disk-shaped morphology. These organisms were identified as responsible for the dechlorination of cis-DCE to ethene in the PCE-dechlorinating consortia, operating together with the Desulfitobacterium as PCE-to-cis-DCE dehalogenating bacterium and with a Syntrophus species as potential hydrogen-producing partner in cultures with benzoate. (orig.)

Bioaugmentation for Remediation of Chlorinated Solvents: Technology Development, Status, and Research Needs

Science.gov (United States)

2005-10-01

perception of GEMs. Bacterial predation by protists has been cited as a factor that could potentially limit the effectiveness of bioaugmentation...It was estimated that protist grazing accounted for approximately 5% of the transported bacteria. However, protists were not abundant until near...injected bacteria. Of note, this predation experiment was conducted in a pristine aquifer. Contaminated aquifers often have concentrations of protists

Monitoring priority substances, other organic contaminants and heavy metals in a volcanic aquifer from different sources and hydrological processes.

Science.gov (United States)

Estevez, Esmeralda; Cabrera, María del Carmen; Fernández-Vera, Juan Ramón; Molina-Díaz, Antonio; Robles-Molina, José; Palacios-Díaz, María del Pino

2016-05-01

Irrigation with reclaimed water (R) is necessary to guarantee the sustainability of semi-arid areas. Results obtained during a two years monitoring network (2009-2011) in Gran Canaria are presented, including the analysis of chemical parameters, N and S isotopes, priority substances (2008/105/EC, 2013/39/EU), other organic contaminants and heavy metals in groundwater and R used to irrigate a golf course. The aims of this work are to evaluate the contamination in a volcanic aquifer, relate the presence of organic contaminants and heavy metals with the hydrogeochemistry and identify pollution sources in the area. No priority substance exceeded the EU thresholds for surface water, although seventeen were detected in R. The most frequent compounds were hexachlorobenzene, chlorpyrifos ethyl, fluorene, phenanthrene and pyrene. These compounds were detected at low concentration, except chlorpyrifos. Chlorpyrifos ethyl, terbuthylazine, diuron, terbutryn, procymidone, atrazine and propazine exceeded the European threshold concentration for pesticides in groundwater (100ngL(-1)). Therefore, the priority substances chlorpyrifos ethyl and diuron must be included in monitoring studies. The priority pesticides chlorfenvinphos and diazinon were always detected in R but rarely in groundwater. Besides, the existence of contaminants not related to the current R irrigation has been identified. Absence of environmental problems related to heavy metals can be expected. The relationship among contaminant presence, hydrogeochemistry, including the stable isotopic prints of δ(18)O, δ(15)N and δ(34)S and preferential recharge paths has been described. The coastal well shows high values of EC, nitrate, a variable chemistry, and 50% of organic contaminants detected above 100ngL(-1). The well located in the recharge area presents a stable hydrochemistry, the lowest value of δ(15)N and the lowest contaminants occurrence. The area is an example of a complex volcanic media with several

Characterization of a managed aquifer recharge system using multiple tracers.

Science.gov (United States)

Moeck, Christian; Radny, Dirk; Popp, Andrea; Brennwald, Matthias; Stoll, Sebastian; Auckenthaler, Adrian; Berg, Michael; Schirmer, Mario

2017-12-31

Knowledge about the residence times of artificially infiltrated water into an aquifer and the resulting flow paths is essential to developing groundwater-management schemes. To obtain this knowledge, a variety of tracers can be used to study residence times and gain information about subsurface processes. Although a variety of tracers exists, their interpretation can differ considerably due to subsurface heterogeneity, underlying assumptions, and sampling and analysis limitations. The current study systematically assesses information gained from seven different tracers during a pumping experiment at a site where drinking water is extracted from an aquifer close to contaminated areas and where groundwater is artificially recharged by infiltrating surface water. We demonstrate that the groundwater residence times estimated using dye and heat tracers are comparable when the thermal retardation for the heat tracer is considered. Furthermore, major ions, acesulfame, and stable isotopes (δ 2 H and δ 18 O) show that mixing of infiltrated water and groundwater coming from the regional flow path occurred and a vertical stratification of the flow system exist. Based on the concentration patterns of dissolved gases (He, Ar, Kr, N 2 , and O 2 ) and chlorinated solvents (e.g., tetrachloroethene), three temporal phases are observed in the ratio between infiltrated water and regional groundwater during the pumping experiment. Variability in this ratio is significantly related to changes in the pumping and infiltration rates. During constant pumping rates, more infiltrated water was extracted, which led to a higher dilution of the regional groundwater. An infiltration interruption caused however, the ratio to change and more regional groundwater is extracted, which led to an increase in all concentrations. The obtained results are discussed for each tracer considered and its strengths and limitations are illustrated. Overall, it is demonstrated that aquifer heterogeneity and

Confined aquifer vulnerability induced by a pumping well in a leakage area

Directory of Open Access Journals (Sweden)

X. Meng

2015-05-01

Full Text Available Due to the pollution of shallow groundwater and the rapid development of society and economy which consume more freshwater, the exploitation of confined groundwater is steadily increasing in north China. Therefore, the rapid decline of the confined groundwater head increases the risk of confined aquifer pollution by leaky recharge from shallow aquifers. In this paper, a quantitative method for assessing confined aquifer vulnerability to contamination due to pumping has been developed. This method is based on the shallow and confined groundwater flow model and the advection and dispersion in the aquitard, including sorption. The cumulative time for the pollutant concentration at the top boundary of confined aquifer exceeding the maximum allowable level is defined as the confined aquifer vulnerability index, which can be obtained by numerically solving the solute transport equation. A hypothetical example is chosen as a case study to illustrate the whole process. The results indicate that the proposed method is a practical and reasonable assessment method of confined aquifer vulnerability.

Source, variability, and transformation of nitrate in a regional karst aquifer: Edwards aquifer, central Texas.

Science.gov (United States)

Musgrove, MaryLynn; Opsahl, Stephen P.; Mahler, Barbara J.; Herrington, Chris; Sample, Thomas; Banta, John

2016-01-01

Many karst regions are undergoing rapid population growth and expansion of urban land accompanied by increases in wastewater generation and changing patterns of nitrate (NO3−) loading to surface and groundwater. We investigate variability and sources of NO3− in a regional karst aquifer system, the Edwards aquifer of central Texas. Samples from streams recharging the aquifer, groundwater wells, and springs were collected during 2008–12 from the Barton Springs and San Antonio segments of the Edwards aquifer and analyzed for nitrogen (N) species concentrations and NO3− stable isotopes (δ15N and δ18O). These data were augmented by historical data collected from 1937 to 2007. NO3− concentrations and discharge data indicate that short-term variability (days to months) in groundwater NO3− concentrations in the Barton Springs segment is controlled by occurrence of individual storms and multi-annual wet-dry cycles, whereas the lack of short-term variability in groundwater in the San Antonio segment indicates the dominance of transport along regional flow paths. In both segments, longer-term increases (years to decades) in NO3− concentrations cannot be attributed to hydrologic conditions; rather, isotopic ratios and land-use change indicate that septic systems and land application of treated wastewater might be the source of increased loading of NO3−. These results highlight the vulnerability of karst aquifers to NO3− contamination from urban wastewater. An analysis of N-species loading in recharge and discharge for the Barton Springs segment during 2008–10 indicates an overall mass balance in total N, but recharge contains higher concentrations of organic N and lower concentrations of NO3−than does discharge, consistent with nitrification of organic N within the aquifer and consumption of dissolved oxygen. This study demonstrates that subaqueous nitrification of organic N in the aquifer, as opposed to in soils, might be a previously

Groundwater vulnerability mapping in Guadalajara aquifers system (Western Mexico)

Science.gov (United States)

Rizo-Decelis, L. David; Marín, Ana I.; Andreo, Bartolomé

2016-04-01

some monitoring wells, which have been related to anthropogenic activity. Vulnerability maps were produced using different parametric methods (e.g.: DRASTIC, GOD, DISCO, AVI), then the results are compared and assessed. Since each one of these methods use different number of parameters and weights, relatively different results were obtained, although the results have been evaluated with common cartographic inputs. The comparison between selected methods shows that the GOD method results are more correlated with the other methods and produces vulnerability maps comparable with them. Even though groundwater vulnerability is a critical issue around the world, no protection zones have been delineated in Guadalajara city, one of the biggest in Latin America. The groundwater contamination in the study area poses a serious risk for a large population and the environment. This work aims to propose an approach for groundwater protection cartography, based on the application and the comparison of results from different contamination vulnerability methods. These outcomes may assist water authorities to identify the higher vulnerable zones of the aquifers, in order to improving and adapting the land planning and management according to the protection of the own water resources.

Geohydrologic units and water-level conditions in the Terrace alluvial aquifer and Paluxy Aquifer, May 1993 and February 1994, near Air Force Plant 4, Fort Worth area, Texas

Science.gov (United States)

Rivers, Glen A.; Baker, Ernest T.; Coplin, L.S.

1996-01-01

The terrace alluvial aquifer underlying Air Force Plant 4 and the adjacent Naval Air Station (formerly Carswell Air Force Base) in the Fort Worth area, Texas, is contaminated locally with organic and metal compounds. Residents south and west of Air Force Plant 4 and the Naval Air Station are concerned that contaminants might enter the underlying Paluxy aquifer, which provides water to the city of White Settlement, south of Air Force Plant 4, and to residents west of Air Force Plant 4. The U.S. Environmental Protection Agency has qualified Air Force Plant 4 for Superfund cleanup. The pertinent geologic units include -A~rom oldest to youngest the Glen Rose, Paluxy, and Walnut Formations, Goodland Limestone, and terrace alluvial deposits. Except for the Glen Rose Formation, all units crop out at or near Air Force Plant 4 and the Naval Air Station. The terrace alluvial deposits, which nearly everywhere form the land surface, range from 0 to about 60 feet thick. These deposits comprise a mostly unconsolidated mixture of gravel, sand, silt, and clay. Mudstone and sandstone of the Paluxy Formation crop out north, west, and southwest of Lake Worth and total between about 130 and about 175 feet thick. The terrace alluvial deposits and the Paluxy Formation comprise the terrace alluvial aquifer and the Paluxy aquifer, respectively. These aquifers are separated by the Goodland-Walnut confining unit, composed of the Goodland Limestone and (or) Walnut Formation. Below the Paluxy aquifer, the Glen Rose Formation forms the Glen Rose confining unit. Water-level measurements during May 1993 and February 1994 from wells in the terrace alluvial aquifer indicate that, regionally, ground water flows toward the east-southeast beneath Air Force Plant 4 and the Naval Air Station. Locally, water appears to flow outward from ground-water mounds maintained by the localized infiltration of precipitation and reportedly by leaking water pipes and sanitary and (or) storm sewer lines beneath the

Mineralization of PAHs in coal-tar impacted aquifer sediments and associated microbial community structure investigated with FISH

Energy Technology Data Exchange (ETDEWEB)

Rogers, S W; Ong, S K; Moorman, T B [Iowa State University, Ames, IA (USA)

2007-11-15

The microbial community structure and mineralization of polycyclic aromatic hydrocarbons (PAHs) in a coal-tar contaminated aquifer were investigated spatially using fluorescence in situ hybridization (FISH) and in laboratory-scale incubations of the aquifer sediments. DAPI-detected microbial populations in the contaminated sediments were three orders of magnitude greater than nearby uncontaminated sediments, suggesting growth on coal-tar constituents in situ. Actinobacteria, {beta}- and {gamma}-Proteobacteria, and Flavobacteria dominated the in situ aerobic (> 1 mg l{sup -1} dissolved oxygen) microbial community, whereas sulfate-reducing bacteria comprised 37% of the microbial community in the sulfidogenic region of the aquifer. Rapid mineralization of naphthalene and phenanthrene were observed in aerobic laboratory microcosms and resulted in significant enrichment of {beta}- and {gamma}-Proteobacteria potentially explaining their elevated presence in situ. Nitrate- and sulfate-limited mineralization of naphthalene in laboratory microcosms occurred to a small degree in aquifer sediments from locations where groundwater chemistry indicated nitrate- and sulfate-reduction, respectively. The results of this study suggest that FISH may be a useful tool for providing a link between laboratory microcosms and groundwater measurements made in situ necessary to better demonstrate the potential for natural attenuation at complex PAH contaminated sites.

Accounting for the Decreasing Reaction Potential of Heterogeneous Aquifers in a Stochastic Framework of Aquifer-Scale Reactive Transport

Science.gov (United States)

Loschko, Matthias; Wöhling, Thomas; Rudolph, David L.; Cirpka, Olaf A.

2018-01-01

Many groundwater contaminants react with components of the aquifer matrix, causing a depletion of the aquifer's reactivity with time. We discuss conceptual simplifications of reactive transport that allow the implementation of a decreasing reaction potential in reactive-transport simulations in chemically and hydraulically heterogeneous aquifers without relying on a fully explicit description. We replace spatial coordinates by travel-times and use the concept of relative reactivity, which represents the reaction-partner supply from the matrix relative to a reference. Microorganisms facilitating the reactions are not explicitly modeled. Solute mixing is neglected. Streamlines, obtained by particle tracking, are discretized in travel-time increments with variable content of reaction partners in the matrix. As exemplary reactive system, we consider aerobic respiration and denitrification with simplified reaction equations: Dissolved oxygen undergoes conditional zero-order decay, nitrate follows first-order decay, which is inhibited in the presence of dissolved oxygen. Both reactions deplete the bioavailable organic carbon of the matrix, which in turn determines the relative reactivity. These simplifications reduce the computational effort, facilitating stochastic simulations of reactive transport on the aquifer scale. In a one-dimensional test case with a more detailed description of the reactions, we derive a potential relationship between the bioavailable organic-carbon content and the relative reactivity. In a three-dimensional steady-state test case, we use the simplified model to calculate the decreasing denitrification potential of an artificial aquifer over 200 years in an ensemble of 200 members. We demonstrate that the uncertainty in predicting the nitrate breakthrough in a heterogeneous aquifer decreases with increasing scale of observation.

Combination of aquifer thermal energy storage and enhanced bioremediation

NARCIS (Netherlands)

Ni, Zhuobiao; Gaans, van Pauline; Smit, Martijn; Rijnaarts, Huub; Grotenhuis, Tim

2016-01-01

To meet the demand for sustainable energy, aquifer thermal energy storage (ATES) is widely used in the subsurface in urban areas. However, contamination of groundwater, especially with chlorinated volatile organic compounds (CVOCs), is often being encountered. This is commonly seen as an

Inventory of drainage wells and potential sources of contaminants to drainage-well inflow in Southwest Orlando, Orange County, Florida

Science.gov (United States)

Taylor, George Fred

1993-01-01

Potential sources of contaminants that could pose a threat to drainage-well inflow and to water in the Floridan aquifer system in southwest Orlando, Florida, were studied between October and December 1990. Drainage wells and public-supply wells were inventoried in a 14-square-mile area, and available data on land use and activities within each drainage well basin were tabulated. Three public-supply wells (tapping the Lower Floridan aquifer) and 38 drainage wells (open to the Upper Floridan aquifer) were located in 17 drainage basins within the study area. The primary sources of drainage-well inflow are lake overflow, street runoff, seepage from the surficial aquifer system, and process-wastewater disposal. Drainage-well inflow from a variety of ares, including resi- dential, commercial, undeveloped, paved, and industrial areas, are potential sources of con- taminants. The four general types of possible contaminants to drainage-well inflow are inorganic chemicals, organic compounds, turbidity, and microbiological contaminants. Potential contami- nant sources include plant nurseries, citrus groves, parking lots, plating companies, auto- motive repair shops, and most commonly, lake- overflow water. Drainage wells provide a pathway for contaminants to enter the Upper Floridan aquifer and there is a potential for contaminants to move downward from the Upper Floridan to the Lower Floridan aquifer.

Identification of immiscible NAPL contaminant sources in aquifers by a modified two-level saturation based imperialist competitive algorithm

Science.gov (United States)

Ghafouri, H. R.; Mosharaf-Dehkordi, M.; Afzalan, B.

2017-07-01

A simulation-optimization model is proposed for identifying the characteristics of local immiscible NAPL contaminant sources inside aquifers. This model employs the UTCHEM 9.0 software as its simulator for solving the governing equations associated with the multi-phase flow in porous media. As the optimization model, a novel two-level saturation based Imperialist Competitive Algorithm (ICA) is proposed to estimate the parameters of contaminant sources. The first level consists of three parallel independent ICAs and plays as a pre-conditioner for the second level which is a single modified ICA. The ICA in the second level is modified by dividing each country into a number of provinces (smaller parts). Similar to countries in the classical ICA, these provinces are optimized by the assimilation, competition, and revolution steps in the ICA. To increase the diversity of populations, a new approach named knock the base method is proposed. The performance and accuracy of the simulation-optimization model is assessed by solving a set of two and three-dimensional problems considering the effects of different parameters such as the grid size, rock heterogeneity and designated monitoring networks. The obtained numerical results indicate that using this simulation-optimization model provides accurate results at a less number of iterations when compared with the model employing the classical one-level ICA. A model is proposed to identify characteristics of immiscible NAPL contaminant sources. The contaminant is immiscible in water and multi-phase flow is simulated. The model is a multi-level saturation-based optimization algorithm based on ICA. Each answer string in second level is divided into a set of provinces. Each ICA is modified by incorporating a new knock the base model.

Source, variability, and transformation of nitrate in a regional karst aquifer: Edwards aquifer, central Texas

Energy Technology Data Exchange (ETDEWEB)

Musgrove, M., E-mail: mmusgrov@usgs.gov [U.S. Geological Survey, 1505 Ferguson Lane, Austin, TX 78754 (United States); Opsahl, S.P. [U.S. Geological Survey, 5563 DeZavala, Ste. 290, San Antonio, TX 78249 (United States); Mahler, B.J. [U.S. Geological Survey, 1505 Ferguson Lane, Austin, TX 78754 (United States); Herrington, C. [City of Austin Watershed Protection Department, Austin, TX 78704 (United States); Sample, T.L. [U.S. Geological Survey, 19241 David Memorial Dr., Ste. 180, Conroe, TX 77385 (United States); Banta, J.R. [U.S. Geological Survey, 5563 DeZavala, Ste. 290, San Antonio, TX 78249 (United States)

2016-10-15

Many karst regions are undergoing rapid population growth and expansion of urban land accompanied by increases in wastewater generation and changing patterns of nitrate (NO{sub 3}{sup −}) loading to surface and groundwater. We investigate variability and sources of NO{sub 3}{sup −} in a regional karst aquifer system, the Edwards aquifer of central Texas. Samples from streams recharging the aquifer, groundwater wells, and springs were collected during 2008–12 from the Barton Springs and San Antonio segments of the Edwards aquifer and analyzed for nitrogen (N) species concentrations and NO{sub 3}{sup −} stable isotopes (δ{sup 15}N and δ{sup 18}O). These data were augmented by historical data collected from 1937 to 2007. NO{sub 3}{sup −} concentrations and discharge data indicate that short-term variability (days to months) in groundwater NO{sub 3}{sup −} concentrations in the Barton Springs segment is controlled by occurrence of individual storms and multi-annual wet-dry cycles, whereas the lack of short-term variability in groundwater in the San Antonio segment indicates the dominance of transport along regional flow paths. In both segments, longer-term increases (years to decades) in NO{sub 3}{sup −} concentrations cannot be attributed to hydrologic conditions; rather, isotopic ratios and land-use change indicate that septic systems and land application of treated wastewater might be the source of increased loading of NO{sub 3}{sup −}. These results highlight the vulnerability of karst aquifers to NO{sub 3}{sup −} contamination from urban wastewater. An analysis of N-species loading in recharge and discharge for the Barton Springs segment during 2008–10 indicates an overall mass balance in total N, but recharge contains higher concentrations of organic N and lower concentrations of NO{sub 3}{sup −} than does discharge, consistent with nitrification of organic N within the aquifer and consumption of dissolved oxygen. This study demonstrates

Source, variability, and transformation of nitrate in a regional karst aquifer: Edwards aquifer, central Texas

International Nuclear Information System (INIS)

Musgrove, M.; Opsahl, S.P.; Mahler, B.J.; Herrington, C.; Sample, T.L.; Banta, J.R.

2016-01-01

Many karst regions are undergoing rapid population growth and expansion of urban land accompanied by increases in wastewater generation and changing patterns of nitrate (NO 3 − ) loading to surface and groundwater. We investigate variability and sources of NO 3 − in a regional karst aquifer system, the Edwards aquifer of central Texas. Samples from streams recharging the aquifer, groundwater wells, and springs were collected during 2008–12 from the Barton Springs and San Antonio segments of the Edwards aquifer and analyzed for nitrogen (N) species concentrations and NO 3 − stable isotopes (δ 15 N and δ 18 O). These data were augmented by historical data collected from 1937 to 2007. NO 3 − concentrations and discharge data indicate that short-term variability (days to months) in groundwater NO 3 − concentrations in the Barton Springs segment is controlled by occurrence of individual storms and multi-annual wet-dry cycles, whereas the lack of short-term variability in groundwater in the San Antonio segment indicates the dominance of transport along regional flow paths. In both segments, longer-term increases (years to decades) in NO 3 − concentrations cannot be attributed to hydrologic conditions; rather, isotopic ratios and land-use change indicate that septic systems and land application of treated wastewater might be the source of increased loading of NO 3 − . These results highlight the vulnerability of karst aquifers to NO 3 − contamination from urban wastewater. An analysis of N-species loading in recharge and discharge for the Barton Springs segment during 2008–10 indicates an overall mass balance in total N, but recharge contains higher concentrations of organic N and lower concentrations of NO 3 − than does discharge, consistent with nitrification of organic N within the aquifer and consumption of dissolved oxygen. This study demonstrates that subaqueous nitrification of organic N in the aquifer, as opposed to in soils, might be a

Fate of nine recycled water trace organic contaminants and metal(loid)s during managed aquifer recharge into a anaerobic aquifer: Column studies.

Science.gov (United States)

Patterson, B M; Shackleton, M; Furness, A J; Pearce, J; Descourvieres, C; Linge, K L; Busetti, F; Spadek, T

2010-03-01

Water quality changes associated with the passage of aerobic reverse osmosis (RO) treated recycled water through a deep anaerobic pyritic aquifer system was evaluated in sediment-filled laboratory columns as part of a managed aquifer recharge (MAR) strategy. The fate of nine recycled water trace organic compounds along with potential negative water quality changes such as the release of metal(loid)s were investigated in large-scale columns over a period of 12 months. The anaerobic geochemical conditions provided a suitable environment for denitrification, and rapid (half-life 100 days). High retardation coefficients (R) determined for many of the trace organics (R 13 to 67) would increase aquifer residence time and be beneficial for many of the slow degrading compounds. However, for the trace organics with low R values (1.1-2.6) and slow degradation rates (half-life > 100 days), such as N-nitrosodimethylamine, N-nitrosomorpholine and iohexol, substantial biodegradation during aquifer passage may not occur and additional investigations are required. Only minor transient increases in some metal(loid) concentrations were observed, as a result of either pyrite oxidation, mineral dissolution or pH induced metal desorption, followed by metal re-sorption downgradient in the oxygen depleted zone. Crown Copyright 2009. Published by Elsevier Ltd. All rights reserved.

Contaminant Attenuation and Transport Characterization of 200-UP-1 Operable Unit Sediment Samples

Energy Technology Data Exchange (ETDEWEB)

Lee, Brady D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Szecsody, James E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Qafoku, Nikolla [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); McElroy, Erin M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Baum, Steven R. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Snyder, Michelle MV [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lawter, Amanda R. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Resch, Charles T. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Gartman, Brandy N. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Zhong, Lirong [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Saunders, Danielle L. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Williams, Benjamin D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Horner, Jacob A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Leavy, Ian I. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Christiansen, Beren B. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Clayton, Ray E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Johnson, Kayla C. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2017-09-27

Contaminants disposed of at the land surface migrate through the vadose zone, forming plumes in groundwater. Processes that occur in the groundwater can attenuate contaminant concentrations during transport through the aquifer. For this reason, quantifying contaminant attenuation and contaminant transport processes in the aquifer, in support of the conceptual site model (CSM) and fate and transport modeling, are important for assessing the need for, and type of, remediation in the groundwater, including monitored natural attenuation (MNA). The framework to characterize attenuation and transport processes provided in U.S. Environmental Protection Agency (EPA) guidance documents was used to guide the laboratory effort reported herein.

The role of alluvial aquifer sediments in attenuating a dissolved arsenic plume.

Science.gov (United States)

Ziegler, Brady A; Schreiber, Madeline E; Cozzarelli, Isabelle M

2017-09-01

In a crude-oil-contaminated sandy aquifer at the Bemidji site in northern Minnesota, biodegradation of petroleum hydrocarbons has resulted in release of naturally occurring As to groundwater under Fe-reducing conditions. This study used chemical extractions of aquifer sediments collected in 1993 and 2011-2014 to evaluate the relationship between Fe and As in different redox zones (oxic, methanogenic, Fe-reducing, anoxic-suboxic transition) of the contaminated aquifer over a twenty-year period. Results show that 1) the aquifer has the capacity to naturally attenuate the plume of dissolved As, primarily through sorption; 2) Fe and As are linearly correlated in sediment across all redox zones, and a regression analysis between Fe and As reasonably predicted As concentrations in sediment from 1993 using only Fe concentrations; 3) an As-rich "iron curtain," associated with the anoxic-suboxic transition zone, migrated 30m downgradient between 1993 and 2013 as a result of the hydrocarbon plume evolution; and 4) silt lenses in the aquifer preferentially sequester dissolved As, though As is remobilized into groundwater from sediment after reducing conditions are established. Using results of this study coupled with historical data, we develop a conceptual model which summarizes the natural attenuation of As and Fe over time and space that can be applied to other sites that experience As mobilization due to an influx of bioavailable organic matter. Copyright © 2017 Elsevier B.V. All rights reserved.

The role of alluvial aquifer sediments in attenuating a dissolved arsenic plume

Science.gov (United States)

Ziegler, Brady A.; Schreiber, Madeline E.; Cozzarelli, Isabelle M.

2017-01-01

In a crude-oil-contaminated sandy aquifer at the Bemidji site in northern Minnesota, biodegradation of petroleum hydrocarbons has resulted in release of naturally occurring As to groundwater under Fe-reducing conditions. This study used chemical extractions of aquifer sediments collected in 1993 and 2011–2014 to evaluate the relationship between Fe and As in different redox zones (oxic, methanogenic, Fe-reducing, anoxic-suboxic transition) of the contaminated aquifer over a twenty-year period. Results show that 1) the aquifer has the capacity to naturally attenuate the plume of dissolved As, primarily through sorption; 2) Fe and As are linearly correlated in sediment across all redox zones, and a regression analysis between Fe and As reasonably predicted As concentrations in sediment from 1993 using only Fe concentrations; 3) an As-rich “iron curtain,” associated with the anoxic-suboxic transition zone, migrated 30 m downgradient between 1993 and 2013 as a result of the hydrocarbon plume evolution; and 4) silt lenses in the aquifer preferentially sequester dissolved As, though As is remobilized into groundwater from sediment after reducing conditions are established. Using results of this study coupled with historical data, we develop a conceptual model which summarizes the natural attenuation of As and Fe over time and space that can be applied to other sites that experience As mobilization due to an influx of bioavailable organic matter.

Aquifer Vulnerability to Arsenic contamination in the Conterminous United States: Health Risks and Economic Implications

Science.gov (United States)

Twarakavi, N. C.; Kaluarachchi, J. J.

2004-12-01

Arsenic is historically known be toxic to human health. Drinking water contaminated with unsafe levels of arsenic may cause cancer. The toxicity of arsenic is suggested by a MCLG of zero and a low MCL of 10 µg/L, that has been a subject of constant scrutiny. The US Environmental Protection Agency (US EPA), based on the recommendations of the National Academy of Sciences revised the MCL from 1974 value of 50 µg/L to 10 µg/L. The decision was based on a national-level analysis of arsenic concentration data collected by the National Analysis of Water Quality Assessment (NAWQA). Another factor that makes arsenic in drinking water a major issue is the widespread occurrence and a variety of sources. Arsenic occurs naturally in mineral deposits and is also contributed through anthropogenic sources. A methodology using the ordinal logistic regression (LR) method is proposed to predict the probability of occurrence of arsenic in shallow ground waters of the conterminous United States (CONUS) subject to a set of influencing variables. The analysis considered the maximum contaminant level (MCL) options of 3, 5, 10, 20, and 50 µg/L as threshold values to estimate the probabilities of arsenic occurrence in ranges defined by a given MCL and a detection limit of 1 µg/L. The fit between the observed and predicted probability of occurrence was around 83% for all MCL options. The estimated probabilities were used to estimate the median background concentration of arsenic for different aquifer types in the CONUS. The shallow ground water of the western US is more vulnerable to arsenic contamination than the eastern US. Arizona, Utah, Nevada, and California in particular are hotspots for arsenic contamination. The model results were extended for estimating the health risks and costs posed by arsenic occurrence in the ground water of the United States. The risk assessment showed that counties in southern California, Arizona, Florida, Washington States and a few others scattered

Final report for the IAEA urban aquifers RCA : determining the effects of storm water infiltration on groundwater quality in an urban fractured rock aquifer, Auckland, New Zealand

International Nuclear Information System (INIS)

Rosen, M.R.; Hong, Y.S.; Sheppard, D.; Roberts, K.; Viljevac, Z.; Smaill, A.; Reeves, R.R.

2000-01-01

Disposal of storm water in the Mt Eden-Mt Albert area of Auckland, New Zealand, is via ''soak holes'' drilled directly into the top of the fractured basalt. These soak holes receive storm water and sediment runoff from city streets throughout Mt Eden. Although this method of disposal has been used for at least 60 years, its sustainability with respect to groundwater quality has not been addressed. This study aimed to determine the impact of soakage on the chemical and isotopic composition of the groundwater. In addition, sediments captured by the soak holes were analysed to determine their effectiveness at trapping contaminants. Groundwater samples were collected between August 1998 and August 1999. Three sampling trips were carried out after rainfall events in October 1998, April 1999 and August 1999. Samples were analysed for major and trace components, including nutrients, dissolved and total heavy metals (As, Cr, Cu, Zn, Pb, Cd, and Ni), polynuclear aromatic hydrocarbons (PAHs), chlorofluorocarbons (CFCs) and stable and radiogenic isotopes. Cores of sediment collected in the soak holes were analysed for major components, total and leachable heavy metals, and PAHs to determine the ability of the sediments to adsorp contaminants. In summary, the Mt Eden aquifer system shows the effect of storm water infiltration rapidly after a rainfall event in some parts of the aquifer. Water quality has been effected in some areas, but in general the water quality is quite good considering the quantity of storm water discharge that has occurred in the area for the past 60 years. The relatively high quality of the water in the wells monitored may be attributed to the ability of the accumulated sediment in the soak holes and the aquifer fractures to trap contaminants. Further research is needed to determine if continued use of the groundwater system as a conduit for storm water infiltration will lead to clogging of the fractures in the aquifer and/or transport of particulates

Elastic Wave Imaging of in-Situ Bio-Alterations in a Contaminated Aquifer

Science.gov (United States)

Jaiswal, P.; Raj, R.; Atekwana, E. A.; Briand, B.; Alam, I.

2014-12-01

We present a pioneering report on the utility of seismic methods in imaging bio-induced elastic property changes within a contaminated aquifer. To understand physical properties of contaminated soil, we acquired 48 meters long multichannel seismic profile over the Norman landfill leachate plume in Norman Oklahoma, USA. We estimated both the P- and S- wave velocities respectively using full-waveform inversion of the transmission and the ground-roll coda. The resulting S-wave model showed distinct velocity anomaly (~10% over background) within the water table fluctuation zone bounded by the historical minimum and maximum groundwater table. In comparison, the P-wave velocity anomaly within the same zone was negligible. The Environmental Scanning Electron Microscope (ESEM) images of samples from a core located along the seismic profile clearly shows presence of biofilms in the water table fluctuation zone and their absence both above and below the fluctuation zone. Elemental chemistry further indicates that the sediment composition throughout the core is fairly constant. We conclude that the velocity anomaly in S-wave is due to biofilms. As a next step, we develop mechanistic modeling to gain insights into the petro-physical behavior of biofilm-bearing sediments. Preliminary results suggest that a plausible model could be biofilms acting as contact cement between sediment grains. The biofilm cement can be placed in two ways - (i) superficial non-contact deposition on sediment grains, and (ii) deposition at grain contacts. Both models explain P- and S- wave velocity structure at reasonable (~5-10%) biofilm saturation and are equivocally supported by the ESEM images. Ongoing attenuation modeling from full-waveform inversion and its mechanistic realization, may be able to further discriminate between the two cement models. Our study strongly suggests that as opposed to the traditional P-wave seismic, S-wave acquisition and imaging can be a more powerful tool for in

Biotransformation of monoaromatic and chlorinated hydrocarbons at an aviation-gasoline spill site

International Nuclear Information System (INIS)

Wilson, B.H.; Wilson, J.T.; Kampbell, D.H.; Bledsoe, B.E.; Armstrong, J.M.

1991-01-01

Loss of petroleum products from underground storage tanks, pipelines, and accidental spills are major sources of contamination of unsaturated soils, aquifer solids, and a shallow water table aquifer under the U.S. Coast Guard Air Station at Traverse City, MI, has acclimated to the aerobic and anaerobic transformation of monoaromatic hydrocarbons (BTX) released from an aviation gasoline spill. The aquifer also exhibits reductive dechlorination of a chlorinated solvent spill adjacent to the aviation gasoline spill. The groundwater is buffered near neutrality. The aviation gasoline plume is methanogenic and the aquifer contains enough iron minerals to support significant iron solubilization. Field evidence of both aerobic and anaerobic biotransformation of monoaromatics was confirmed by laboratory studies of aquifer material obtained from the site. In the laboratory studies, the removal of the monoaromatics in the anaerobic material was rapid and compared favorable with removal in the aerobic material. The kinetics of anaerobic removal of monoaromatics in the laboratory were similar to the kinetics at field scale in the aquifer. Biotransformation of the chlorinated solvents was not observed until late in the study, when daughter products from reductive dechlorination of the chlorinated solvents were identified by GC/MS

Advances in hydrocarbons spill remediation in Barreal-Belen: proposed measures for the protection of aquifers

International Nuclear Information System (INIS)

Vargas Fallas, Luis Carlos

2011-01-01

The advances accomplished with regard to hydrocarbons spill remediation, through 2009 are shown and the costs made in the process are listed. In the Central Valley have been located about 160 gas stations on major aquifers at risk of contamination, in light of the case of hydrocarbons spill happened in Barreal-Belen in 2004, discovered by chance during the inspection to a nearby well. The study instruments of the vulnerability to contamination of aquifers are analyzed. A proposal of measures is presented, which should be taken to ensure control over the risk of further spillage and for proper management of waters. (author) [es

Modelling of contaminant release from a uranium mine tailings site

International Nuclear Information System (INIS)

Kahnt, Rene; Metschies, Thomas

2007-01-01

Available in abstract form only. Full text of publication follows: Uranium mining and milling continuing from the early 1960's until 1990 close to the town of Seelingstaedt in Eastern Germany resulted in 4 tailings impoundments with a total tailings volume of about 105 Mio. m 3 . Leakage from these tailings impoundments enters the underlying aquifers and is discharged into surface water streams. High concentration of salts, uranium and several heavy metals are released from the tailings. At present the tailings impoundments are reshaped and covered. For the identification of suitable remediation options predictions of the contaminant release for different remediation scenarios have to be made. A compartment model representing the tailings impoundments and the surrounding aquifers for the calculation of contaminant release and transport was set up using the software GOLDSIM. This compartment model describes the time dependent hydraulic conditions within the tailings and the surrounding aquifers taking into account hydraulic and geotechnical processes influencing the hydraulic properties of the tailings material. A simple geochemical approach taking into account sorption processes as well as retardation by applying a k d -approach was implemented to describe the contaminant release and transport within the hydraulic system. For uranium as the relevant contaminant the simple approach takes into account additional geochemical conditions influencing the mobility. Alternatively the model approach allows to include the results of detailed geochemical modelling of the individual tailings zones which is than used as source term for the modelling of the contaminant transport in the aquifer and to the receiving streams. (authors)

Solvent Handbook Database System user's manual

International Nuclear Information System (INIS)

1993-03-01

Industrial solvents and cleaners are used in maintenance facilities to remove wax, grease, oil, carbon, machining fluids, solder fluxes, mold release, and various other contaminants from parts, and to prepare the surface of various metals. However, because of growing environmental and worker-safety concerns, government regulations have already excluded the use of some chemicals and have restricted the use of halogenated hydrocarbons because they affect the ozone layer and may cause cancer. The Solvent Handbook Database System lets you view information on solvents and cleaners, including test results on cleaning performance, air emissions, recycling and recovery, corrosion, and non-metals compatibility. Company and product safety information is also available

Hydrogeological modelling of the Atlantis aquifer for management ...

African Journals Online (AJOL)

The Atlantis Water Supply Scheme (AWSS, Western Cape, South Africa) has been in operation for about 40 years as a means to supply and augment drinking water to the town of Atlantis via managed aquifer recharge (MAR). In this study, the numerical model MODFLOW for groundwater flow and contaminant transport was ...

A method to investigate inter-aquifer leakage using hydraulics and multiple environmental tracers

Science.gov (United States)

Priestley, Stacey; Love, Andrew; Wohling, Daniel; Post, Vincent; Shand, Paul; Kipfer, Rolf; Tyroller, Lina

2016-04-01

Informed aquifer management decisions regarding sustainable yields or potential exploitation require an understanding of the groundwater system (Alley et al. 2002, Cherry and Parker 2004). Recently, the increase in coal seam gas (CSG) or shale gas production has highlighted the need for a better understanding of inter-aquifer leakage and contaminant migration. In most groundwater systems, the quantity or location of inter-aquifer leakage is unknown. Not taking into account leakage rates in the analysis of large scale flow systems can also lead to significant errors in the estimates of groundwater flow rates in aquifers (Love et al. 1993, Toth 2009). There is an urgent need for robust methods to investigate inter-aquifer leakage at a regional scale. This study builds on previous groundwater flow and inter-aquifer leakage studies to provide a methodology to investigate inter-aquifer leakage in a regional sedimentary basin using hydraulics and a multi-tracer approach. The methodology incorporates geological, hydrogeological and hydrochemical information in the basin to determine the likelihood and location of inter-aquifer leakage. Of particular benefit is the analysis of hydraulic heads and environmental tracers at nested piezometers, or where these are unavailable bore couplets comprising bores above and below the aquitard of interest within a localised geographical area. The proposed methodology has been successful in investigating inter-aquifer leakage in the Arckaringa Basin, South Australia. The suite of environmental tracers and isotopes used to analyse inter-aquifer leakage included the stable isotopes of water, radiocarbon, chloride-36, 87Sr/86Sr and helium isotopes. There is evidence for inter-aquifer leakage in the centre of the basin ~40 km along the regional flow path. This inter-aquifer leakage has been identified by a slight draw-down in the upper aquifer during pumping in the lower aquifer, overlap in Sr isotopes, δ2H, δ18O and chloride

Long-distance electron transfer by cable bacteria in aquifer sediments

DEFF Research Database (Denmark)

Müller, Hubert; Bosch, Julian; Griebler, Christian

2016-01-01

recycling of sulfate by electron transfer over 1–2-cm distance. Sediments were taken from a hydrocarbon-contaminated aquifer, amended with iron sulfide and saturated with water, leaving the sediment surface exposed to air. Steep geochemical gradients developed in the upper 3 cm, showing a spatial separation...... recently been discovered in marine sediments to couple spatially separated redox half reactions over centimeter scales. Here we provide primary evidence that such sulfur-oxidizing cable bacteria can also be found at oxic–anoxic interfaces in aquifer sediments, where they provide a means for the direct...

Assessment of Groundwater Susceptibility to Non-Point Source Contaminants Using Three-Dimensional Transient Indexes.

Science.gov (United States)

Zhang, Yong; Weissmann, Gary S; Fogg, Graham E; Lu, Bingqing; Sun, HongGuang; Zheng, Chunmiao

2018-06-05

Groundwater susceptibility to non-point source contamination is typically quantified by stable indexes, while groundwater quality evolution (or deterioration globally) can be a long-term process that may last for decades and exhibit strong temporal variations. This study proposes a three-dimensional (3- d ), transient index map built upon physical models to characterize the complete temporal evolution of deep aquifer susceptibility. For illustration purposes, the previous travel time probability density (BTTPD) approach is extended to assess the 3- d deep groundwater susceptibility to non-point source contamination within a sequence stratigraphic framework observed in the Kings River fluvial fan (KRFF) aquifer. The BTTPD, which represents complete age distributions underlying a single groundwater sample in a regional-scale aquifer, is used as a quantitative, transient measure of aquifer susceptibility. The resultant 3- d imaging of susceptibility using the simulated BTTPDs in KRFF reveals the strong influence of regional-scale heterogeneity on susceptibility. The regional-scale incised-valley fill deposits increase the susceptibility of aquifers by enhancing rapid downward solute movement and displaying relatively narrow and young age distributions. In contrast, the regional-scale sequence-boundary paleosols within the open-fan deposits "protect" deep aquifers by slowing downward solute movement and displaying a relatively broad and old age distribution. Further comparison of the simulated susceptibility index maps to known contaminant distributions shows that these maps are generally consistent with the high concentration and quick evolution of 1,2-dibromo-3-chloropropane (DBCP) in groundwater around the incised-valley fill since the 1970s'. This application demonstrates that the BTTPDs can be used as quantitative and transient measures of deep aquifer susceptibility to non-point source contamination.

Fate of N-nitrosomorpholine in an anaerobic aquifer used for managed aquifer recharge: a column study.

Science.gov (United States)

Pitoi, M M; Patterson, B M; Furness, A J; Bastow, T P; McKinley, A J

2011-04-01

The fate of N-nitrosomorpholine (NMOR) was evaluated at microgram and nanogram per litre concentrations. Experiments were undertaken to simulate the passage of groundwater contaminants through a deep anaerobic pyritic aquifer system, as part of a managed aquifer recharge (MAR) strategy. Sorption studies demonstrated the high mobility of NMOR in the Leederville aquifer system, with retardation coefficients between 1.2 and 1.6. Degradation studies from a 351 day column experiment and a 506 day stop-flow column experiment showed an anaerobic biologically induced reductive degradation process which followed first order kinetics. A biological lag-time of less than 3 months and a transient accumulation of morpholine (MOR) were also noted during the degradation. Comparable half-life degradation rates of 40-45 days were observed over three orders of magnitude in concentration (200 ng L(-1) to 650 μg L(-1)). An inhibitory effect on microorganism responsible to the biodegradation of NMOR at 650 μg L(-1) or a threshold effect at 200 ng L(-1) was not observed during these experiments. Crown Copyright © 2011. Published by Elsevier Ltd. All rights reserved.

Pump-and-treat is not the only solution to aquifer remediation

International Nuclear Information System (INIS)

Odermatt, J.R.

1994-01-01

The Environmental Protection Agency (EPA) recently surveyed remediation technologies used at petroleum-contaminated sites in 22 states. About 96 percent of underground storage tank (UST) corrective action sites used some form of pump-and-treat technology to remediate contaminated groundwater. However, using only pump-and-treat technology is not a cost-effective approach to aquifer remediation. Pump-and-treat may be more appropriate for containing plumes or for use in initial emergency response actions at sites and massive NAPL releases to groundwater. As of 1990, 68 percent of Superfund records of decision selected pump-and-treat as the final remedy for aquifer remediation. However, of 13 sites where the remedial alternative objective was to restore the aquifer to health-based levels, only one pump-and-treat method has succeeded. Except in cases where human health and the environment are threatened, long-term active technologies, such as pump-and-treat, may not be warranted. Groundwater monitoring and possible wellhead treatment may be perceived as time-consuming processes; however, at many sites, this long-term approach may be far less costly and just as effective as other long-term strategies based on exclusive use of pump-and-treat technology

Aquifer characteristics and groundwater recharge pattern in a typical ...

African Journals Online (AJOL)

EJIRO

method in the delineation of bedrock structures, depth to possible aquifer units and to ... makes for susceptibility to surface contaminants; and (iii) ... regional tectonic setting which are critical to identifying favourable ... Data acquisition and processing. Thirty four ... The VES analysis shows a minimum of three and a maximum ...

Fast-track aquifer characterization and bioremediation of groundwater

International Nuclear Information System (INIS)

Owen, S.B.; Erskine, J.A.; Adkisson, C.

1995-01-01

A short duration step-drawdown pumping test has been used to characterize a highly permeable aquifer contaminated with petroleum hydrocarbons in support of an in situ, closed loop extraction and reinjection bioremediation system for groundwater. The short-term pumping test produces a manageable quantity of contaminated groundwater while yielding a range of values for transmissivity and specific yield parameters. This range of aquifer coefficients is used in an analytical model to estimate a range of groundwater extraction rates that provide a suitable radius of influence for the extraction and reinjection system. A multi-enzyme complex catalyzed bioremediation process has been used to aerobically degrade petroleum hydrocarbons. Enzymes, amino acids, and biosurfactants are supplied to the extracted groundwater to significantly speed up the degradation by naturally occurring bacteria. During the process, amino acids promote the rapid growth of the microbial population while enzymes and bacteria attach to hydrocarbons forming a transformation state complex that degrades to fatty acids, carbon dioxide, and water. This paper presents a case study of a fast-track bioremediation using pumping test data, analytical modeling, and an enzyme technology

Hydrochemistry of New Zealand's aquifers

International Nuclear Information System (INIS)

Rosen, M.R.

2001-01-01

Groundwater chemistry on a national scale has never been studied in New Zealand apart from a few studies on nitrate concentrations and pesticides. These studies are covered in Chapter 8 of this book. However general studies of groundwater chemistry, groundwater-rock interaction and regional characteristics of water quality have not been previously addressed in much detail. This is partly because New Zealand aquifers are relatively small on a world scale and are geologically and tectonically diverse (see Chapter 3). But New Zealand has also recently lacked a centralised agency responsible for groundwater quality, and therefore, no national assessments have been undertaken. In recent years, the Institute of Geological and Nuclear Sciences has managed a programme of collecting and analysing the groundwater chemistry of key New Zealand aquifers. This programme is called the National Groundwater Monitoring Programme (NGMP) and is funded by the New Zealand Public Good Science Fund. The programme started in 1990 using only 22 wells, with four regional authorities of the country participating. The NGMP now includes all 15 regional and unitary authorities that use groundwater and over 100 monitoring sites. The NGMP is considered a nationally significant database by the New Zealand Foundation for Research Science and Technology. The NGMP allows a national comparison of aquifer chemistries because the samples are all analysed at one laboratory in a consistent manner and undergo stringent quality control checks. Poor quality analyses are thus minimised. In addition, samples are collected quarterly so that long-term seasonal trends in water quality can be analysed, and the effects of changes in land use and the vulnerability of aquifers to contaminant leaching can be assessed. This chapter summarises the water quality data collected for the NGMP over the past 10 years. Some records are much shorter than others, but most are greater than three years. Additional information is

Potential effect of natural gas wells on alluvial groundwater contamination at the Kansas City Plant

Energy Technology Data Exchange (ETDEWEB)

Pickering, D.A.; Laase, A.D. [Oak Ridge National Lab., TN (United States); Locke, D.A. [Oak Ridge Inst. for Science and Education, TN (United States)

1993-05-01

This report is the result of a request for further information about several abandoned natural gas wells at the US Department of Energy`s Kansas City Plant (KCP). The request was prompted by an old map showing several, possibly eight, natural gas wells located under or near what is now the southeast corner of the Main Manufacturing Building at KCP. Volatile organic compound contamination in the alluvial aquifer surrounding the gas wells might possibly contaminate the bedrock aquifer if the gas wells still exist as conduits. Several circumstances exist that make it doubtful that contamination is entering the bedrock aquifers: (1) because regional groundwater flow in the bedrock beneath the KCP is expected to be vertically upward, contaminants found in the alluvial aquifer should not migrate down the old wells; (2) because of the low hydraulic conductivity of the bedrock units, contaminant transport would be extremely slow if the contaminants were migrating down the wells; and (3) casing, apparently set through the alluvium in all of the wells, would have deteriorated and may have collapsed; if the casing collapsed, the silty clays in the alluvium would also collapse and seal the well. No definitive information has been discovered about the exact location of the wells. No further search for or consideration of the old gas wells is recommended.

Potential effect of natural gas wells on alluvial groundwater contamination at the Kansas City Plant

Energy Technology Data Exchange (ETDEWEB)

Pickering, D.A.; Laase, A.D. (Oak Ridge National Lab., TN (United States)); Locke, D.A. (Oak Ridge Inst. for Science and Education, TN (United States))

1993-05-01

This report is the result of a request for further information about several abandoned natural gas wells at the US Department of Energy's Kansas City Plant (KCP). The request was prompted by an old map showing several, possibly eight, natural gas wells located under or near what is now the southeast corner of the Main Manufacturing Building at KCP. Volatile organic compound contamination in the alluvial aquifer surrounding the gas wells might possibly contaminate the bedrock aquifer if the gas wells still exist as conduits. Several circumstances exist that make it doubtful that contamination is entering the bedrock aquifers: (1) because regional groundwater flow in the bedrock beneath the KCP is expected to be vertically upward, contaminants found in the alluvial aquifer should not migrate down the old wells; (2) because of the low hydraulic conductivity of the bedrock units, contaminant transport would be extremely slow if the contaminants were migrating down the wells; and (3) casing, apparently set through the alluvium in all of the wells, would have deteriorated and may have collapsed; if the casing collapsed, the silty clays in the alluvium would also collapse and seal the well. No definitive information has been discovered about the exact location of the wells. No further search for or consideration of the old gas wells is recommended.

Potential effect of natural gas wells on alluvial groundwater contamination at the Kansas City Plant

International Nuclear Information System (INIS)

Pickering, D.A.; Laase, A.D.; Locke, D.A.

1993-05-01

This report is the result of a request for further information about several abandoned natural gas wells at the US Department of Energy's Kansas City Plant (KCP). The request was prompted by an old map showing several, possibly eight, natural gas wells located under or near what is now the southeast corner of the Main Manufacturing Building at KCP. Volatile organic compound contamination in the alluvial aquifer surrounding the gas wells might possibly contaminate the bedrock aquifer if the gas wells still exist as conduits. Several circumstances exist that make it doubtful that contamination is entering the bedrock aquifers: (1) because regional groundwater flow in the bedrock beneath the KCP is expected to be vertically upward, contaminants found in the alluvial aquifer should not migrate down the old wells; (2) because of the low hydraulic conductivity of the bedrock units, contaminant transport would be extremely slow if the contaminants were migrating down the wells; and (3) casing, apparently set through the alluvium in all of the wells, would have deteriorated and may have collapsed; if the casing collapsed, the silty clays in the alluvium would also collapse and seal the well. No definitive information has been discovered about the exact location of the wells. No further search for or consideration of the old gas wells is recommended

Mapping of coastal aquifer vulnerable zone in the south west coast of Kanyakumari, South India, using GIS-based DRASTIC model.

Science.gov (United States)

Kaliraj, S; Chandrasekar, N; Peter, T Simon; Selvakumar, S; Magesh, N S

2015-01-01

The south west coast of Kanyakumari district in Tamil Nadu, India, is significantly affected by seawater intrusion and diffusion of pollutants into the aquifers due to unregulated beach placer mining and other anthropogenic activities. The present study investigates the vulnerability of the coastal aquifers using Geographic Information System (GIS)-based DRASTIC model. The seven DRASTIC parameters have been analyzed using the statistical equation of this model to demarcate the vulnerable zones for aquifer contamination. The vulnerability index map is prepared from the weighted spatial parameters, and an accounting of total index value ranged from 85 to 213. Based on the categorization of vulnerability classes, the high vulnerable zones are found near the beach placer mining areas between Manavalakurichi and Kodimanal coastal stretches. The aquifers associated with settlements and agricultural lands in the middle-eastern part have experienced high vulnerability due to contaminated water bodies. Similarly, the coastal areas of Thengapattinam and Manakudi estuary and around the South Tamaraikulam have also been falling under high vulnerability condition due to backwater and saltpan. In general, the nearshore region except the placer mining zone and the backwater has a moderately vulnerable condition, and the vulnerability index values range from 149 to180. Significantly, the northern and northeastern uplands and some parts of deposition zones in the middle-south coast have been identified as low to no vulnerable conditions. They are structurally controlled by various geological features such as charnockite, garnet biotite gneiss and granites, and sand dunes, respectively. The aquifer vulnerability assessment has been cross-verified by geochemical indicators such as total dissolved solids (TDS), Cl(-), HCO₃(-), and Cl(-)/HCO₃(-) ratio. The high ranges of TDS (1,842--3,736 mg/l) and Cl(-) (1,412--2,112 mg/l) values are well correlated with the observed high

Subsurface contaminant transport from the liquid disposal area, CRNL

International Nuclear Information System (INIS)

Killey, R.W.D.; Munch, J.H.

1984-01-01

This report summarizes geologic, hydrogeologic and geochemical information obtained from a detailed study of the aquifer receiving contaminated waste-waters from the Chemical Pit. Geologically, the study area features wind-deposited sand overlying a continuous lacustrine clayey silt and a bouldery basal till. Medium to coarse sands locally found at the base of the sand sequence appear to represent stream channel deposits following a buried drainage course towards Perch Lake. These channel sands significantly influence groundwater flow; 3-dimensional models will be required to mathematically simulate the system. Based on the subsurface data, calculated groundwater residence times between the infiltration pit and points of discharge to surface into the East Swamp range from 4 to 22 months. The shortest observed residence time for a non-reactive radio-nuclide is 5 months. Tritium data confirm that contamination is confined to the sands, but show that within the sand aquifer there is considerable heterogeneity in the distribution and rates of groundwater flow. Samples of contaminated groundwaters collected during this study featured increased redox potentials, increased acidity, and minor increases in some major ions relative to local uncontaminated groundwater. Extensive oxidation of the sands in contaminated portions of the aquifer may reflect much greater chemical differences in plume groundwaters in the past

Dendrochemistry of multiple releases of chlorinated solvents at a former industrial site

Science.gov (United States)

Balouet, Jean Christophe; Burken, Joel G.; Karg, Frank; Vroblesky, Don; Smith, Kevin T.; Grudd, Hakan; Rindby, Anders; Beaujard, Francois; Chalot, Michel

2012-01-01

Trees can take up and assimilate contaminants from the soil, subsurface, and groundwater. Contaminants in the transpiration stream can become bound or incorporated into the annual rings formed in trees of the temperate zones. The chemical analysis of precisely dated tree rings, called dendrochemistry, can be used to interpret past plant interactions with contaminants. This investigation demonstrates that dendrochemistry can be used to generate historical scenarios of past contamination of groundwater by chlorinated solvents at a site in Verl, Germany. Increment cores from trees at the Verl site were collected and analyzed by energy-dispersive X-ray fluorescence (EDXRF) line scanning. The EDXRF profiles showed four to six time periods where tree rings had anomalously high concentrations of chlorine (Cl) as an indicator of potential contamination by chlorinated solvents.

GROUND WATER ISSUE: STEAM INJECTION FOR SOIL AND AQUIFER REMEDIATION

Science.gov (United States)

The purpose of this Issue Paper is to provide to those involved in assessing remediation technologies for specific sites basic technical information on the use of steam injection for the remediation of soils and aquifers that are contaminated by volatile or semivolatile organic c...

Monitoring priority substances, other organic contaminants and heavy metals in a volcanic aquifer from different sources and hydrological processes

International Nuclear Information System (INIS)

Estevez, Esmeralda; Cabrera, María del Carmen; Fernández-Vera, Juan Ramón; Molina-Díaz, Antonio; Robles-Molina, José; Palacios-Díaz, María del Pino

2016-01-01

Irrigation with reclaimed water (R) is necessary to guarantee the sustainability of semi-arid areas. Results obtained during a two years monitoring network (2009–2011) in Gran Canaria are presented, including the analysis of chemical parameters, N and S isotopes, priority substances (2008/105/EC, 2013/39/EU), other organic contaminants and heavy metals in groundwater and R used to irrigate a golf course. The aims of this work are to evaluate the contamination in a volcanic aquifer, relate the presence of organic contaminants and heavy metals with the hydrogeochemistry and identify pollution sources in the area. No priority substance exceeded the EU thresholds for surface water, although seventeen were detected in R. The most frequent compounds were hexachlorobenzene, chlorpyrifos ethyl, fluorene, phenanthrene and pyrene. These compounds were detected at low concentration, except chlorpyrifos. Chlorpyrifos ethyl, terbuthylazine, diuron, terbutryn, procymidone, atrazine and propazine exceeded the European threshold concentration for pesticides in groundwater (100 ng L"−"1). Therefore, the priority substances chlorpyrifos ethyl and diuron must be included in monitoring studies. The priority pesticides chlorfenvinphos and diazinon were always detected in R but rarely in groundwater. Besides, the existence of contaminants not related to the current R irrigation has been identified. Absence of environmental problems related to heavy metals can be expected. The relationship among contaminant presence, hydrogeochemistry, including the stable isotopic prints of δ"1"8O, δ"1"5N and δ"3"4S and preferential recharge paths has been described. The coastal well shows high values of EC, nitrate, a variable chemistry, and 50% of organic contaminants detected above 100 ng L"−"1. The well located in the recharge area presents a stable hydrochemistry, the lowest value of δ"1"5N and the lowest contaminants occurrence. The area is an example of a complex volcanic media with

Monitoring priority substances, other organic contaminants and heavy metals in a volcanic aquifer from different sources and hydrological processes

Energy Technology Data Exchange (ETDEWEB)

Estevez, Esmeralda, E-mail: eestevez@proyinves.ulpgc.es [Dpt. Física (GEOVOL), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas de Gran Canaria, Canary Islands (Spain); Agrifood and Phytopathological Laboratory (Cabildo de Gran Canaria), 35413 Arucas, Canary Islands (Spain); Cabrera, María del Carmen, E-mail: mcarmen.cabrera@ulpgc.es [Dpt. Física (GEOVOL), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas de Gran Canaria, Canary Islands (Spain); IMDEA Water Institute, Alcalá de Henares, Madrid (Spain); Fernández-Vera, Juan Ramón, E-mail: jrfernandezv@grancanaria.com [Agrifood and Phytopathological Laboratory (Cabildo de Gran Canaria), 35413 Arucas, Canary Islands (Spain); Molina-Díaz, Antonio, E-mail: amolina@ujaen.es [Analytical Chemistry Research Group, Department of Physical and Analytical Chemistry, University of Jaen, 23071 Jaen (Spain); Robles-Molina, José, E-mail: jroblesmol@gmail.com [Analytical Chemistry Research Group, Department of Physical and Analytical Chemistry, University of Jaen, 23071 Jaen (Spain); Palacios-Díaz, María del Pino, E-mail: mp.palaciosdiaz@ulpgc.es [Dpt. de Patología Animal, Producción Animal, Bromatología y Tecnología de los Alimentos (GEOVOL), Universidad de Las Palmas de Gran Canaria, 35413 Arucas, Canary Islands (Spain)

2016-05-01

Irrigation with reclaimed water (R) is necessary to guarantee the sustainability of semi-arid areas. Results obtained during a two years monitoring network (2009–2011) in Gran Canaria are presented, including the analysis of chemical parameters, N and S isotopes, priority substances (2008/105/EC, 2013/39/EU), other organic contaminants and heavy metals in groundwater and R used to irrigate a golf course. The aims of this work are to evaluate the contamination in a volcanic aquifer, relate the presence of organic contaminants and heavy metals with the hydrogeochemistry and identify pollution sources in the area. No priority substance exceeded the EU thresholds for surface water, although seventeen were detected in R. The most frequent compounds were hexachlorobenzene, chlorpyrifos ethyl, fluorene, phenanthrene and pyrene. These compounds were detected at low concentration, except chlorpyrifos. Chlorpyrifos ethyl, terbuthylazine, diuron, terbutryn, procymidone, atrazine and propazine exceeded the European threshold concentration for pesticides in groundwater (100 ng L{sup −1}). Therefore, the priority substances chlorpyrifos ethyl and diuron must be included in monitoring studies. The priority pesticides chlorfenvinphos and diazinon were always detected in R but rarely in groundwater. Besides, the existence of contaminants not related to the current R irrigation has been identified. Absence of environmental problems related to heavy metals can be expected. The relationship among contaminant presence, hydrogeochemistry, including the stable isotopic prints of δ{sup 18}O, δ{sup 15}N and δ{sup 34}S and preferential recharge paths has been described. The coastal well shows high values of EC, nitrate, a variable chemistry, and 50% of organic contaminants detected above 100 ng L{sup −1}. The well located in the recharge area presents a stable hydrochemistry, the lowest value of δ{sup 15}N and the lowest contaminants occurrence. The area is an example of a complex

Use of Additives in Bioremediation of Contaminated Groundwater and Soil

Science.gov (United States)

This chapter reviews application of additives used in bioremediation of chlorinated solvents and fuels for groundwater and soil remediation. Soluble carbon substrates are applicable to most site conditions except aquifers with very high or very low groundwater flow. Slow-release ...

Migration of chlorinated hydrocarbons in multilayer unconsolidated porous media: a case study from the Po Plain, Italy

Directory of Open Access Journals (Sweden)

Maria Filippini

2017-12-01

Full Text Available Chlorinated solvents are the most ubiquitous organic contaminants found in groundwater since the last six decades. Due to their high degree of carcinogenicity/toxicity and the relatively high mobility and persistence, they represent a serious threat against the human health and the environment. These contaminants generally reach groundwater as Dense Non-Aqueous Phase Liquid (DNAPL that can migrate through aquifers easier than aqueous contaminants. The complex phase partitioning to which chlorinated solvent DNAPLs can undergo (i.e. to the dissolved, vapor or sorbed phase, as well as their transformations (e.g. degradation, depend on the physico-chemical properties of the contaminants and on the features of the hydrogeological system in which they migrate. The hydrogeologic setting below the city of Ferrara (Po plain, northern Italy, which is affected by scattered contamination by chlorinated solvents, has been investigated. In particular, a limited-inspace high-resolution investigation was performed in one selected contaminated test-site, known as “Caretti site”. Here, high-resolution vertical profiling of different kind of data (i.e. stratigraphic data, hydraulic heads, hydrochemical composition of water, stable isotopes of water and contaminants were collected by means of multilevel monitoring systems and other innovative sampling and analytical techniques. The main goals of the research were to assess the intrinsic vulnerability of the aquifers and to identify the dynamics of migration and transformation of the chloroethene contaminants in relationship to the features of the hosting porous medium. The confined aquifers turned out to be more vulnerable to DNAPLs than aqueous contaminants due to the occurrence of microfractures in the overlying clayey aquitards. The presence of organic-rich deposits in the local stratigraphy enhanced the biodegradation of chloroethenes causing accumulation of Vinyl Chloride. The results are useful at the

Contamination of surface and underground waters owing to the disaster of the Sasa mine tailing pond

OpenAIRE

Mircovski, Vojo; Spasovski, Orce

2003-01-01

The uncontrolled run off of flotation waste from the Sasa Mine causes contamination of the flows of the Rivers Kamenicka and Bregalnica as well as the water of Kalimanci Lake and further afield. Boundary, fracture and karst type of aquifers formed depending on the structural type of porosity along the marginal parts of the terrain. The aquifers are recharged mostly by the above mentioned rivers that results in contamination of their waters. Contamination of underground waters is particularly ...

Inherent mineralization of 2,6-dichlorobenzamide (BAM) in unsaturated zone and aquifers - Effect of initial concentrations and adaptation

Energy Technology Data Exchange (ETDEWEB)

Janniche, Gry Sander, E-mail: gsja@env.dtu.dk [DTU Environment, Technical University of Denmark, Building 113, DK-2800 Kgs. Lyngby (Denmark); Clausen, Liselotte; Albrechtsen, Hans-Jorgen [DTU Environment, Technical University of Denmark, Building 113, DK-2800 Kgs. Lyngby (Denmark)

2011-10-15

The dichlobenil metabolite BAM (2,6-dichlorobenzamide) is frequently detected in aquifers e.g. in Denmark despite the mother compound dichlobenil was banned here since 1997. BAM mineralization was investigated at environmentally relevant concentrations in sediment samples. Undisturbed sediment cores with known dichlobenil application were collected from topsoil to 8.5 m below surface resulting in 57 samples hereof 4 aquifer samples. Mineralization was only substantial (>10%) in the uppermost meter of the unsaturated zone. Microbial adaptation, observed as faster mineralization in pre-exposed than in pristine sediments from the same location, was only evident in sandy sediment where dichlobenil was still present, but not in clayey sediments. Higher initial concentrations (1-5000 {mu}g/kg) did not stimulate mineralization in pristine clayey or sandy sediments, or in pre-exposed sand. However, in pre-exposed clay mineralization was stimulated at high concentrations. Furthermore BAM was for the first time mineralized in aerobic aquifer sediments from different BAM-contaminated groundwater locations. - Highlights: > BAM mineralized in BAM-contaminated aerobic aquifer sediments. > In subsurface, fastest BAM mineralization in pre-exposed sandy sediments. > Increased mineralization (adaptation) only observed in contaminated sandy sediment. > In pristine sediments mineralization ratio increased with decreasing concentrations. - BAM mineralization in subsurface and groundwater was demonstrated.

Semianalytical Solutions for Transport in Aquifer and Fractured Clay Matrix System

Science.gov (United States)

A three-dimensional mathematical model that describes transport of contaminant in a horizontal aquifer with simultaneous diffusion into a fractured clay formation is proposed. A group of analytical solutions is derived based on specific initial and boundary conditions as well as ...

Time scales of DNAPL migration in sandy aquifers examined via numerical simulation

Energy Technology Data Exchange (ETDEWEB)

Gerhard, J.I.; Pang, T.; Kueper, B.H. [University of Edinburgh, Edinburgh (United Kingdom). Inst. of Infrastructure & Environmental

2007-03-15

The time required for dense nonaqueous phase liquid (DNAPL) to cease migrating following release to the subsurface is a valuable component of a site conceptual model. This study uses numerical simulation to investigate the migration of six different DNAPLs in sandy aquifers. The most influential parameters governing migration cessation time are the density and viscosity of the DNAPL and the mean hydraulic conductivity of the aquifer. Releases of between 1 and 40 drums of chlorinated solvent DNAPLs, characterized by relatively high density and low viscosity, require on the order of months to a few years to cease migrating in a heterogeneous medium sand aquifer having an average hydraulic conductivity of 7.4 x 10{sup -3} cm/s. In contrast to this, the release of 20 drums of coal tar {rho}{sub D} = 1061 kg/m{sup 3}, {mu}{sub D} = 0.161 Pa(.)s) requires more than 100 years to cease migrating in the same aquifer. Altering the mean hydraulic conductivity of the aquifer results in a proportional change in cessation times. Parameters that exhibit relatively little influence on migration time scales are the DNAPL-water interfacial tension, release volume, source capillary pressure, mean aquifer porosity, and ambient ground water hydraulic gradient. This study also demonstrates that low-density DNAPLs (e.g., coal tar) give rise to greater amounts of lateral spreading and greater amounts of pooling on capillary barriers than high-density DNAPLs such as trichloroethylene or tetrachloroethylene.

Analytical evaluation of the radionuclide concentration through the aquifer for the Abadia de Goias Repository

International Nuclear Information System (INIS)

Alves, Antonio Sergio de Martin

1999-01-01

In this paper the radionuclide concentration though the aquifer has been determined by an analytical process considering that the radionuclide migration is influenced by two kinds of radionuclides releases from the repository during an overflow. In the first release it is assumed that when the radionuclides reach the aquifer there is no contamination in it and the release rate is a constant. For this case it is utilized the model of Reference. For the subsequent releases there will be a contamination in the aquifer provenient from the former releases; it is considered that the subsequent releases are a function of the time which, for the Abadia de Goias Repository, was determined in the Reference. The Laplace transform Method has been utilized to solve the Radionuclide Migration Transport Equation in the aquifer region for the subsequent releases and the resulting function is expressed in terms of exponential and complementary error functions. The improvement in the calculation model, presented in this paper, can be used in the safety analysis of repositories, contributing thus in the nuclear waste management field and particularly, being connecting also to the environmental protection concern. (author)

The EED [Emergencies Engineering Division] solvent extraction process for the removal of petroleum-derived hydrocarbons from soil

International Nuclear Information System (INIS)

Bastien, C.Y.

1994-03-01

Research was conducted to investigate the ability of hexane and natural gas condensate (NGC) to extract three different types of hydrocarbon contaminant (light crude oil, diesel fuel, and bunker C oil) from three types of soil (sand, peat, and clay). A separate but related study determined the efficiency of solvent extraction (using hexane and five other solvents but not NGC) for removal of polychlorinated biphenyls (PCB) from contaminated soil. The process developed for this research includes stages of mixing, extraction, separation, and solvent recovery, for eventual implementation as a mobile solvent extraction unit. In experiments on samples created in the laboratory, extraction efficiencies of hydrocarbons often rose above 95%. On samples from a petroleum contaminated site, average extraction efficiency was ca 82%. Sandy soils contaminated in the laboratory were effectively cleaned of all hydrocarbons tested but only diesel fuel was successfully extracted from peat soils. No significant differences were observed in the effectiveness of hexane and NGC for contamination levels above 3%. Below this number, NGC seems more effective at removing oil from peat while hexane is slightly more effective on clay soils. Sand is equally cleaned by both solvents at all contamination levels. Safety considerations, odor, extra care needed to deal with light ends and aromatics, and the fact that only 26% of the solvent is actually usable make NGC an unfeasible option in spite of its significantly lower cost compared to hexane. For extracting PCBs, a hexane/acetone mixture proved to have the best removal efficiency. 14 refs., 14 figs., 7 tabs

Removal of iron contaminant from zirconium chloride solution

International Nuclear Information System (INIS)

Voit, D.O.

1992-01-01

This patent describes a process for eliminating iron contaminant from an aqueous zirconium chloride solution that has been contaminated with FeCl 3 in a plant in which zirconium and hafnium chloride solutions are separated by a main MINK solvent extraction system and the FeCl 3 is normally removed from the zirconium chloride solution by a secondary MINK solvent extraction system

In situ treatment of arsenic contaminated groundwater by aquifer iron coating: Experimental study

Energy Technology Data Exchange (ETDEWEB)

Xie, Xianjun, E-mail: xjxie@cug.edu.cn [State Key Laboratory of Biogeology and Environmental Geology, School of Environmental Studies, China University of Geosciences, 430074 Wuhan (China); Wang, Yanxin, E-mail: yx.wang@cug.edu.cn [State Key Laboratory of Biogeology and Environmental Geology, School of Environmental Studies, China University of Geosciences, 430074 Wuhan (China); Pi, Kunfu [State Key Laboratory of Biogeology and Environmental Geology, School of Environmental Studies, China University of Geosciences, 430074 Wuhan (China); Liu, Chongxuan [State Key Laboratory of Biogeology and Environmental Geology, School of Environmental Studies, China University of Geosciences, 430074 Wuhan (China); Pacific Northwest National Laboratory, Richland, WA 99354 (United States); Li, Junxia; Liu, Yaqing; Wang, Zhiqiang; Duan, Mengyu [State Key Laboratory of Biogeology and Environmental Geology, School of Environmental Studies, China University of Geosciences, 430074 Wuhan (China)

2015-09-15

In situ arsenic removal from groundwater by an aquifer iron coating method has great potential to be a cost effective and simple groundwater remediation technology, especially in rural and remote areas where groundwater is used as the main water source for drinking. The in situ arsenic removal technology was first optimized by simulating arsenic removal in various quartz sand columns under anoxic conditions. The effectiveness was then evaluated in an actual high-arsenic groundwater environment. The arsenic removal mechanism by the coated iron oxide/hydroxide was investigated under different conditions using scanning electron microscopy (SEM)/X-ray absorption spectroscopy, electron probe microanalysis, and Fourier transformation infrared spectroscopy. Aquifer iron coating method was developed via a 4-step alternating injection of oxidant, iron salt and oxygen-free water. A continuous injection of 5.0 mmol/L FeSO{sub 4} and 2.5 mmol/L NaClO for 96 h can form a uniform goethite coating on the surface of quartz sand without causing clogging. At a flow rate of 7.2 mL/min of the injection reagents, arsenic (as Na{sub 2}HAsO{sub 4}) and tracer fluorescein sodium to pass through the iron-coated quartz sand column were approximately at 126 and 7 column pore volumes, respectively. The retardation factor of arsenic was 23.0, and the adsorption capacity was 0.11 mol As per mol Fe. In situ arsenic removal from groundwater in an aquifer was achieved by simultaneous injections of As(V) and Fe(II) reagents. Arsenic fixation resulted from a process of adsorption/co-precipitation with fine goethite particles by way of bidentate binuclear complexes. Therefore, the study results indicate that the high arsenic removal efficiency of the in situ aquifer iron coating technology likely resulted from the expanded specific surface area of the small goethite particles, which enhanced arsenic sorption capability and/or from co-precipitation of arsenic on the surface of goethite particles

In situ treatment of arsenic contaminated groundwater by aquifer iron coating: Experimental study

International Nuclear Information System (INIS)

Xie, Xianjun; Wang, Yanxin; Pi, Kunfu; Liu, Chongxuan; Li, Junxia; Liu, Yaqing; Wang, Zhiqiang; Duan, Mengyu

2015-01-01

In situ arsenic removal from groundwater by an aquifer iron coating method has great potential to be a cost effective and simple groundwater remediation technology, especially in rural and remote areas where groundwater is used as the main water source for drinking. The in situ arsenic removal technology was first optimized by simulating arsenic removal in various quartz sand columns under anoxic conditions. The effectiveness was then evaluated in an actual high-arsenic groundwater environment. The arsenic removal mechanism by the coated iron oxide/hydroxide was investigated under different conditions using scanning electron microscopy (SEM)/X-ray absorption spectroscopy, electron probe microanalysis, and Fourier transformation infrared spectroscopy. Aquifer iron coating method was developed via a 4-step alternating injection of oxidant, iron salt and oxygen-free water. A continuous injection of 5.0 mmol/L FeSO 4 and 2.5 mmol/L NaClO for 96 h can form a uniform goethite coating on the surface of quartz sand without causing clogging. At a flow rate of 7.2 mL/min of the injection reagents, arsenic (as Na 2 HAsO 4 ) and tracer fluorescein sodium to pass through the iron-coated quartz sand column were approximately at 126 and 7 column pore volumes, respectively. The retardation factor of arsenic was 23.0, and the adsorption capacity was 0.11 mol As per mol Fe. In situ arsenic removal from groundwater in an aquifer was achieved by simultaneous injections of As(V) and Fe(II) reagents. Arsenic fixation resulted from a process of adsorption/co-precipitation with fine goethite particles by way of bidentate binuclear complexes. Therefore, the study results indicate that the high arsenic removal efficiency of the in situ aquifer iron coating technology likely resulted from the expanded specific surface area of the small goethite particles, which enhanced arsenic sorption capability and/or from co-precipitation of arsenic on the surface of goethite particles. - Highlights: �

A long-term bench-scale investigation of permanganate consumption by aquifer materials.

Science.gov (United States)

Xu, Xiuyuan; Thomson, Neil R

2009-11-20

In situ chemical oxidation (ISCO) applications using permanganate involve the injection or release of permanganate into the subsurface to destroy various target contaminants. Naturally occurring reduced components associated with aquifer materials can exert a significant oxidant demand thereby reducing the amount of permanganate available for the destruction of contaminants as well as reducing the overall rate of oxidation. Quantification of this natural oxidant demand (NOD) is a requirement for site-specific assessment and the design of cost-effective oxidant delivery systems. To further our understanding of the interaction between permanganate and aquifer materials, aerobic and anaerobic aquifer materials from eight representative sites throughout North America were tested in a series of systematic bench-scale experiments. Various permanganate to aquifer solids mass loading ratios at different initial permanganate concentrations in well-mixed batch reactors were monitored for >300 days. All NOD temporal profiles demonstrated an initial fast consumption rate followed by a persistent slower consumption rate. The data generated show that the mass loading ratio, the initial permanganate concentration, and the nature and quantity of reduced aquifer material species are the main factors controlling permanganate consumption rates. A higher initial permanganate concentration or a larger mass loading ratio produced a larger fast NOD consumption rate and generated a corresponding higher maximum NOD value. Hence, both the NOD temporal profile and the maximum NOD are not single-valued but are heavily dependent on the experimental conditions. Predictive relationships were developed to estimate the maximum NOD and the NOD at 7 days based on aquifer material properties. The concentration of manganese oxides deposited on the aquifer solids was highly correlated with the mass of permanganate consumed suggesting that passivation of NOD reaction sites occurred due to the formation

Developing a probability-based model of aquifer vulnerability in an agricultural region

Science.gov (United States)

Chen, Shih-Kai; Jang, Cheng-Shin; Peng, Yi-Huei

2013-04-01

SummaryHydrogeological settings of aquifers strongly influence the regional groundwater movement and pollution processes. Establishing a map of aquifer vulnerability is considerably critical for planning a scheme of groundwater quality protection. This study developed a novel probability-based DRASTIC model of aquifer vulnerability in the Choushui River alluvial fan, Taiwan, using indicator kriging and to determine various risk categories of contamination potentials based on estimated vulnerability indexes. Categories and ratings of six parameters in the probability-based DRASTIC model were probabilistically characterized according to the parameter classification methods of selecting a maximum estimation probability and calculating an expected value. Moreover, the probability-based estimation and assessment gave us an excellent insight into propagating the uncertainty of parameters due to limited observation data. To examine the prediction capacity of pollutants for the developed probability-based DRASTIC model, medium, high, and very high risk categories of contamination potentials were compared with observed nitrate-N exceeding 0.5 mg/L indicating the anthropogenic groundwater pollution. The analyzed results reveal that the developed probability-based DRASTIC model is capable of predicting high nitrate-N groundwater pollution and characterizing the parameter uncertainty via the probability estimation processes.

Arsenic release during managed aquifer recharge (MAR)

Science.gov (United States)

Pichler, T.; Lazareva, O.; Druschel, G.

2013-12-01

The mobilization and addition of geogenic trace metals to groundwater is typically caused by anthropogenic perturbations of the physicochemical conditions in the aquifer. This can add dangerously high levels of toxins to groundwater, thus compromising its use as a source of drinking water. In several regions world-wide, aquifer storage and recovery (ASR), a form of managed aquifer recharge (MAR), faces the problem of arsenic release due to the injection of oxygenated storage water. To better understand this process we coupled geochemical reactive transport modeling to bench-scale leaching experiments to investigate and verify the mobilization of geogenic arsenic (As) under a range of redox conditions from an arsenic-rich pyrite bearing limestone aquifer in Central Florida. Modeling and experimental observations showed similar results and confirmed the following: (1) native groundwater and aquifer matrix, including pyrite, were in chemical equilibrium, thus preventing the release of As due to pyrite dissolution under ambient conditions; (2) mixing of oxygen-rich surface water with oxygen-depleted native groundwater changed the redox conditions and promoted the dissolution of pyrite, and (3) the behavior of As along a flow path was controlled by a complex series of interconnected reactions. This included the oxidative dissolution of pyrite and simultaneous sorption of As onto neo-formed hydrous ferric oxides (HFO), followed by the reductive dissolution of HFO and secondary release of adsorbed As under reducing conditions. Arsenic contamination of drinking water in these systems is thus controlled by the re-equilibration of the system to more reducing conditions rather than a purely oxidative process.

Remediating Contaminant Plumes in Groundwater with Shallow Excavations Containing Coarse Reactive Media.

Science.gov (United States)

Hudak, Paul F

2018-02-01

A groundwater flow and mass transport model tested the capability of shallow excavations filled with coarse, reactive media to remediate a hypothetical unconfined aquifer with a maximum saturated thickness of 5 m. Modeled as contaminant sinks, the rectangular excavations were 10 m downgradient of an initial contaminant plume originating from a source at the top of the aquifer. The initial plume was approximately 259 m long, 23 m wide, and 5 m thick, with a downgradient tip located approximately 100 m upgradient of the site boundary. The smallest trench capable of preventing offsite migration was 11 m long (measured perpendicular to groundwater flow), 4 m wide (measured parallel to groundwater flow), and 3 m deep. Results of this study suggest that shallow trenches filled with coarse filter media that partially penetrate unconfined aquifers may be a viable alternative for remediating contaminated groundwater at some sites.

Development Report on the Idaho National Laboratory Sitewide Three-Dimensional Aquifer Model

Energy Technology Data Exchange (ETDEWEB)

Thomas R. Wood; Catherine M. Helm-Clark; Hai Huang; Swen Magnuson; Travis McLing; Brennon Orr; Michael J. Rohe; Mitchell A. Plummer; Robert Podgorney; Erik Whitmore; Michael S. Roddy

2007-09-01

A sub-regional scale, three-dimensional flow model of the Snake River Plain Aquifer was developed to support remediation decisions for Waste Area Group 10, Operable Unit 10 08 at the Idaho National Laboratory (INL) Site. This model has been calibrated primarily to water levels and secondarily to groundwater velocities interpreted from stable isotope disequilibrium studies and the movement of anthropogenic contaminants in the aquifer from facilities at the INL. The three-dimensional flow model described in this report is one step in the process of constructing a fully three-dimensional groundwater flow and contaminant transport model as prescribed in the Idaho National Engineering and Environmental Laboratory Operable Unit 10-08 Sitewide Groundwater Model Work Plan. An updated three-dimensional hydrogeologic conceptual model is presented along with the geologic basis for the conceptual model. Sediment-dominated three-dimensional volumes were used to represent the geology and constrain groundwater flow as part of the conceptual model. Hydrological, geochemical, and geological data were summarized and evaluated to infer aquifer behavior. A primary observation from development and evaluation of the conceptual model was that relative to flow on a regional scale, the aquifer can be treated with steady-state conditions. Boundary conditions developed for the three-dimensional flow model are presented along with inverse simulations that estimate parameterization of hydraulic conductivity. Inverse simulations were performed using the pilot-point method to estimate permeability distributions. Thermal modeling at the regional aquifer scale and at the sub-regional scale using the inverted permeabilities is presented to corroborate the results of the flow model. The results from the flow model show good agreement with simulated and observed water levels almost always within 1 meter. Simulated velocities show generally good agreement with some discrepancies in an interpreted low

Characterizing fate and transport properties in karst aquifers under different hydrologic conditions

Science.gov (United States)

Rodriguez, E.; Padilla, I. Y.

2017-12-01

Karst landscapes contain very productive aquifers. The hydraulic and hydrogeological characteristics of karst aquifers make these systems capable of storing and transporting large amount of water, but also highly vulnerable to contamination. Their extremely heterogeneous nature prevents accurate prediction in contaminant fate and transport. Even more challenging is to understand the impact of hydrologic conditions changes on fate and transport processes. This studies aims at characterizing fate and transport processes in the karst groundwater system of northern Puerto Rico under different hydrologic conditions. The study involves injecting rhodamine and uranine dyes into a sinkhole, and monitoring concentrations at a spring. Results show incomplete recovery of tracers, but breaking curves can be used to estimate advective, dispersive and mass transfer characteristic of the karst system. Preliminary results suggest significant differences in fate and transport characteristics under different hydrologic conditions.

Determining Changes in Groundwater Quality during Managed Aquifer Recharge

Science.gov (United States)

Gambhir, T.; Houlihan, M.; Fakhreddine, S.; Dadakis, J.; Fendorf, S. E.

2016-12-01

Managed aquifer recharge (MAR) is becoming an increasingly prevalent technology for improving the sustainability of freshwater supply. However, recharge water can alter the geochemical conditions of the aquifer, mobilizing contaminants native to the aquifer sediments. Geochemical alterations on deep (>300 m) injection of highly treated recycled wastewater for MAR has received limited attention. We aim to determine how residual disinfectants used in water treatment processes, specifically the strong oxidants chloramine and hydrogen peroxide, affect metal mobilization within deep injection wells of the Orange County Water District. Furthermore, as the treated recharge water has very low ionic strength (44.6 mg L-1 total dissolved solids), we tested how differing concentrations of magnesium chloride and calcium chloride affected metal mobilization within deep aquifers. Continuous flow experiments were conducted on columns dry packed with sediments from a deep injection MAR site in Orange County, CA. The effluent was analyzed for shifts in water quality, including aqueous concentrations of arsenic, uranium, and chromium. Interaction between the sediment and oxic recharge solution causes naturally-occurring arsenopyrite to repartition onto iron oxides. The stability of arsenic on the newly precipitated iron oxides is dependent on pH changes during recharge.

Groundwater redox conditions and conductivity in a contaminant plume from geoelectrical investigations

Directory of Open Access Journals (Sweden)

V. Naudet

2004-01-01

Full Text Available Accurate mapping of the electrical conductivity and of the redox potential of the groundwater is important in delineating the shape of a contaminant plume. A map of redox potential in an aquifer is indicative of biodegradation of organic matter and of concentrations of redox-active components; a map of electrical conductivity provides information on the mineralisation of the groundwater. Both maps can be used to optimise the position of pumping wells for remediation. The self-potential method (SP and electrical resistivity tomography (ERT have been applied to the contaminant plume associated with the Entressen landfill in south-east France. The self-potential depends on groundwater flow (electrokinetic contribution and redox conditions ('electro-redox' contribution. Using the variation of the piezometric head in the aquifer, the electrokinetic contribution is removed from the SP signals. A good linear correlation (R2=0.85 is obtained between the residual SP data and the redox potential values measured in monitoring wells. This relationship is used to draw a redox potential map of the overall contaminated site. The electrical conductivity of the subsoil is obtained from 3D-ERT analysis. A good linear correlation (R2=0.91 is observed between the electrical conductivity of the aquifer determined from the 3D-ERT image and the conductivity of the groundwater measured in boreholes. This indicates that the formation factor is nearly homogeneous in the shallow aquifer at the scale of the ERT. From this correlation, a map of the pore water conductivity of the aquifer is obtained. Keywords: self-potential, redox potential, electrical resistivity tomography, fluid conductivity, contaminant plume

Aquifer restoration at uranium in situ leach sites

International Nuclear Information System (INIS)

Anastasi, F.S.; Williams, R.E.

1985-01-01

In situ mining of uranium involves injection of a leaching solution (lixiviant) into an ore-bearing aquifer. Frequently, the ground water in the mined aquifer is a domestic or livestock water supply. As the lixiviant migrates through the ore body, uranium and various associated elements such as arsenic, selenium, molybdenum, vanadium and radium-226 are mobilized in the ground water. Aquifer restoration after in situ mining is not fully understood. Several methods have been developed to restore mined aquifers to pre-mining (baseline) quality. Commonly used methods include ground water sweeping, clean water injection, and treatment by ion exchange and reverse osmosis technologies. Ammonium carbonate lixiviant was used at one RandD in situ mine. Attempts were made to restore the aquifer using a variety of methods. Efforts were successful in reducing concentrations of the majority of contaminants to baseline levels. Concentrations of certain parameters, however, remained at levels above baseline six months after restoration ceased. Relatively large quantities of ground water were processed in the restoration attempt considering the small size of the project (1.25 acre). More thorough characterization of the hydrogeology of the site may have enhanced the effectiveness of restoration and reduced potential environmental impacts associated with the project. This paper presents some of the findings of a research project conducted by the Mineral Resources Waste Management Team at the University of Idaho in Moscow, Idaho. Views contained herein do not reflect U.S. Nuclear Regulatory Commission policy

Sources of high-chloride water and managed aquifer recharge in an alluvial aquifer in California, USA

Science.gov (United States)

O'Leary, David R.; Izbicki, John A.; Metzger, Loren F.

2015-11-01

As a result of pumping in excess of recharge, water levels in alluvial aquifers within the Eastern San Joaquin Groundwater Subbasin, 130 km east of San Francisco (California, USA), declined below sea level in the early 1950s and have remained so to the present. Chloride concentrations in some wells increased during that time and exceeded the US Environmental Protection Agency's secondary maximum contaminant level of 250 mg/L, resulting in removal of some wells from service. Sources of high-chloride water include irrigation return in 16 % of sampled wells and water from delta sediments and deeper groundwater in 50 % of sampled wells. Chloride concentrations resulting from irrigation return commonly did not exceed 100 mg/L, although nitrate concentrations were as high as 25 mg/L as nitrogen. Chloride concentrations ranged from less than 100-2,050 mg/L in wells affected by water from delta sediments and deeper groundwater. Sequential electromagnetic logs show movement of high-chloride water from delta sediments to pumping wells through permeable interconnected aquifer layers. δD and δ18O data show most groundwater originated as recharge along the front of the Sierra Nevada, but tritium and carbon-14 data suggest recharge rates in this area are low and have decreased over recent geologic time. Managed aquifer recharge at two sites show differences in water-level responses to recharge and in the physical movement of recharged water with depth related to subsurface geology. Well-bore flow logs also show rapid movement of water from recharge sites through permeable interconnected aquifer layers to pumping wells.

Sources of high-chloride water and managed aquifer recharge in an alluvial aquifer in California, USA

Science.gov (United States)

O'Leary, David; Izbicki, John A.; Metzger, Loren F.

2015-01-01

As a result of pumping in excess of recharge, water levels in alluvial aquifers within the Eastern San Joaquin Groundwater Subbasin, 130 km east of San Francisco (California, USA), declined below sea level in the early 1950s and have remained so to the present. Chloride concentrations in some wells increased during that time and exceeded the US Environmental Protection Agency’s secondary maximum contaminant level of 250 mg/L, resulting in removal of some wells from service. Sources of high-chloride water include irrigation return in 16 % of sampled wells and water from delta sediments and deeper groundwater in 50 % of sampled wells. Chloride concentrations resulting from irrigation return commonly did not exceed 100 mg/L, although nitrate concentrations were as high as 25 mg/L as nitrogen. Chloride concentrations ranged from less than 100–2,050 mg/L in wells affected by water from delta sediments and deeper groundwater. Sequential electromagnetic logs show movement of high-chloride water from delta sediments to pumping wells through permeable interconnected aquifer layers. δD and δ18O data show most groundwater originated as recharge along the front of the Sierra Nevada, but tritium and carbon-14 data suggest recharge rates in this area are low and have decreased over recent geologic time. Managed aquifer recharge at two sites show differences in water-level responses to recharge and in the physical movement of recharged water with depth related to subsurface geology. Well-bore flow logs also show rapid movement of water from recharge sites through permeable interconnected aquifer layers to pumping wells.

Analysis of petroleum-contaminated soils by diffuse reflectance spectroscopy and sequential ultrasonic solvent extraction–gas chromatography

International Nuclear Information System (INIS)

Okparanma, Reuben N.; Coulon, Frederic; Mouazen, Abdul M.

2014-01-01

In this study, we demonstrate that partial least-squares regression analysis with full cross-validation of spectral reflectance data estimates the amount of polycyclic aromatic hydrocarbons in petroleum-contaminated tropical rainforest soils. We applied the approach to 137 field-moist intact soil samples collected from three oil spill sites in Ogoniland in the Niger Delta province (5.317°N, 6.467°E), Nigeria. We used sequential ultrasonic solvent extraction–gas chromatography as the reference chemical method. We took soil diffuse reflectance spectra with a mobile fibre-optic visible and near-infrared spectrophotometer (350–2500 nm). Independent validation of combined data from studied sites showed reasonable prediction precision (root-mean-square error of prediction = 1.16–1.95 mg kg −1 , ratio of prediction deviation = 1.86–3.12, and validation r 2 = 0.77–0.89). This suggests that the methodology may be useful for rapid assessment of the spatial variability of polycyclic aromatic hydrocarbons in petroleum-contaminated soils in the Niger Delta to inform risk assessment and remediation. -- Highlights: • We model NIR diffuse reflectance spectra for PAH prediction in contaminated soils. • Soil diffuse reflectance decreases with increasing PAH concentration. • Mechanism of prediction relies on co-variation of PAH with other soil properties. • Positions of important wavelengths are largely similar for studied sites. • Positive regression coefficients around 1647 nm show a link to PAH. -- This approach may be used to collect large spatial data at reduced cost and time to assess the variability of polycyclic aromatic hydrocarbons in petroleum release sites

Groundwater Remediation in a Floodplain Aquifer at Shiprock, New Mexico

Energy Technology Data Exchange (ETDEWEB)

Peterson, Dave [Navarro Research and Engineering; Miller, David [Navarro Research and Engineering; Kautsky, Mark [U. S. Department of Energy, Office of Legacy Management; Dander, David [Navarro Research and Engineering; Nofchissey, Joni [Navajo Nation Division of Natural Resources

2016-03-06

A uranium- and vanadium-ore-processing mill operated from 1954 to 1968 within the Navajo Nation near Shiprock, New Mexico. By September 1986, all tailings and structures on the former mill property were encapsulated in a disposal cell built on top of two existing tailings piles on the Shiprock site (the site) [1]. Local groundwater was contaminated by multiple inorganic constituents as a result of the milling operations. The U.S. Department of Energy (DOE) took over management of the site in 1978 as part of the Uranium Mill Tailings Remedial Action (UMTRA) Project. The DOE Office of Legacy Management currently manages ongoing activities at the former mill facility, including groundwater remediation. Remediation activities are designed primarily to reduce the concentrations and total plume mass of the mill-related contaminants sulfate, uranium, and nitrate. In addition to contaminating groundwater in alluvial and bedrock sediments directly below the mill site, ore processing led to contamination of a nearby floodplain bordering the San Juan River. Groundwater in a shallow alluvial aquifer beneath the floodplain is strongly influenced by the morphology of the river channel as well as changing flows in the river, which provides drainage for regional runoff from the San Juan Mountains of Colorado. As part of a recent study of the floodplain hydrology, a revised conceptual model was developed for the alluvial aquifer along with an updated status of contaminant plumes that have been impacted by more than 10 years of groundwater pumping for site remediation purposes. Several findings from the recent study will be discussed here.

Geochemical Triggers of Arsenic Mobilization during Managed Aquifer Recharge.

Science.gov (United States)

Fakhreddine, Sarah; Dittmar, Jessica; Phipps, Don; Dadakis, Jason; Fendorf, Scott

2015-07-07

Mobilization of arsenic and other trace metal contaminants during managed aquifer recharge (MAR) poses a challenge to maintaining local groundwater quality and to ensuring the viability of aquifer storage and recovery techniques. Arsenic release from sediments into solution has occurred during purified recycled water recharge of shallow aquifers within Orange County, CA. Accordingly, we examine the geochemical processes controlling As desorption and mobilization from shallow, aerated sediments underlying MAR infiltration basins. Further, we conducted a series of batch and column experiments to evaluate recharge water chemistries that minimize the propensity of As desorption from the aquifer sediments. Within the shallow Orange County Groundwater Basin sediments, the divalent cations Ca(2+) and Mg(2+) are critical for limiting arsenic desorption; they promote As (as arsenate) adsorption to the phyllosilicate clay minerals of the aquifer. While native groundwater contains adequate concentrations of dissolved Ca(2+) and Mg(2+), these cations are not present at sufficient concentrations during recharge of highly purified recycled water. Subsequently, the absence of dissolved Ca(2+) and Mg(2+) displaces As from the sediments into solution. Increasing the dosages of common water treatment amendments including quicklime (Ca(OH)2) and dolomitic lime (CaO·MgO) provides recharge water with higher concentrations of Ca(2+) and Mg(2+) ions and subsequently decreases the release of As during infiltration.

Evaluation of organic contamination in urban groundwater surrounding a municipal landfill, Zhoukou, China.

Science.gov (United States)

Han, D M; Tong, X X; Jin, M G; Hepburn, Emily; Tong, C S; Song, X F

2013-04-01

This paper investigates the organic pollution status of shallow aquifer sediments and groundwater around Zhoukou landfill. Chlorinated aliphatic hydrocarbons, monocylic aromatic hydrocarbons, halogenated aromatic hydrocarbons, organochlorine pesticides and other pesticides, and polycyclic aromatic hydrocarbons (PAHs) have been detected in some water samples. Among the detected eleven PAHs, phenanthrene, fluorine, and fluoranthene are the three dominant in most of the groundwater samples. Analysis of groundwater samples around the landfill revealed concentrations of PAHs ranging from not detected to 2.19 μg/L. The results show that sediments below the waste dump were low in pollution, and the shallow aquifer, at a depth of 18-30 m, was heavily contaminated, particularly during the wet season. An oval-shaped pollution halo has formed, spanning 3 km from west to east and 2 km from south to north, and mainly occurs in groundwater depths of 2-4 m. For PAH source identification, both diagnostic ratios of selected PAHs and principal component analysis were studied, suggesting mixed sources of pyro- and petrogenic derived PAHs in the Zhoukou landfill. Groundwater table fluctuations play an important role in the distribution of organic pollutants within the shallow aquifer. A conceptual model of leachate migration in the Quaternary aquifers surrounding the Zhoukou landfill has been developed to describe the contamination processes based on the major contaminant (PAHs). The groundwater zone contaminated by leachate has been identified surrounding the landfill.

Solvent extraction of radionuclides from aqueous tank waste

International Nuclear Information System (INIS)

Moyer, B.A.; Bonnesen, P.V.; Sachleben, R.A.

1997-01-01

This task aims toward the development of efficient solvent-extraction processes for the removal of the fission products 99 Tc, 90 Sr, and 137 Cs from alkaline tank wastes. Processes already developed or proposed entail direct treatment of the waste solution with the solvent and subsequent stripping of the extracted contaminants from the solvent into a dilute aqueous solution. Working processes to remove Tc(and SR) separately and Cs separately have been developed; the feasibility of a combined process is under investigation. Since Tc, Sr, and Cs will be vitrified together in the high-level fraction, however, a process that could separate Tc, Sr, and Cs simultaneously, as opposed to sequentially, potentially offers the greatest impact. A figure presents a simplified diagram of a proposed solvent-extraction cycle followed by three possible treatments for the stripping solution. Some degree of recycle of the stripping solution (option a) is expected. Simple evaporation (option c) is possible prior to vitrification; this offers the greatest possible volume reduction with simple operation and no consumption of chemicals, but it is energy intensive. However, if the contaminants are concentrated (option b) by fixed-bed technology, the energy penalty of evaporation can be avoided and vitrification facilitated without any additional secondary waste being produced

DNAPL migration in a coastal plain aquifer

International Nuclear Information System (INIS)

DiGuiseppi, W.H.; Jung, A.D.

1995-01-01

Soil and ground water at the Dover Gas Light Superfund Site, a former manufactured gas plant (1859 to 1948), are contaminated with polynuclear aromatic hydrocarbons and volatile organic compounds. Contaminants of concern include light aromatics, such as benzene, toluene, ethylbenzene, and xylenes (BTEX), and heavy aromatics, including naphthalene, acenaphthylene, phenanthrene, and benzo(a)pyrene. Although ground-water contaminant levels are elevated near the site, only naphthalene and acenaphthylene are present within an order of magnitude of their solubility limits, indicating the possibility of dense non-aqueous phase liquids (DNAPL) in the subsurface. The unconfined Columbia Aquifer, which is characterized by interfingering and discontinuous sand, silt, and clay Coastal Plain deposits, overlies a clay aquitard at a depth of 60 feet. The ground water beneath the intermediate clay horizon exhibited little or no contamination, even immediately downgradient from the site. The relationship between the more permeable granular sand horizons and the less permeable interfingering clay zones controls the migration of both the aqueous-phase contamination and the DNAPL. A detailed horizontal and vertical characterization of the subsurface stratigraphy was critical to the accurate interpretation of the extent and magnitude of contamination and the identification and delineation of DNAPL zones

Blast fracturing of bedrock to enhance recovery of contaminated groundwater

International Nuclear Information System (INIS)

Holzman, L.R.; Harvey, E.M.; McKee, R.C.E.; Katsabanis, T.

1992-01-01

Petroleum hydrocarbons releasd from a pipeline at a site in southern Ontario had contaminated a fractured dolostone bedrock aquifer. To remediate the site, contaminated groundwater was pumped from the downgradient edge of the hydrocarbon plume and injected into an upgradient area after treatment. Contaminant flow pathways in the fractured bedrock aquifer were found to be complex and erratic. It was anticipated that contaminated groundwater could escape the influence of a line of closely spaced recovery wells. In order to capture the migrating contaminants effectively, improve communication between recovery wells, and optimize pumping efficiencies, a rubble zone was created by drilling and blasting the rock. Using 140 blastholes, the bedrock was fractured to a depth of 4 m over a distance of 200 m. Similarly, an additional 80 blastholes were used to blast fracture 100 m of bedrock to a depth of 4 m in the recharge area to enhance injection of treated water to the aquifer. Various blasthole spacings and explosive loadings and patterns were tested to fracture the rock effectively while minimizing the impact on the nearby pipeline and neighboring residences. Vibrations were carefully monitored using several seismographs. Pump tests conducted before and after the blast indicated the hydraulic connection between the naturally occurring fractures had greatly improved. Monitoring conducted after startup of the pump-treat-and-inject system has confirmed the fracturing provides effective capture and injection of the groundwater. 3 refs., 3 figs., 1 tab

Ground-water flow in the surficial aquifer system and potential movement of contaminants from selected waste-disposal sites at Naval Station Mayport, Florida

Science.gov (United States)

Halford, K.J.

1998-01-01

Ground-water flow through the surficial aquifer system at Naval Station Mayport near Jacksonville, Florida, was simulated with a two-layer finite-difference model as part of an investigation conducted by the U.S. Geological Survey. The model was calibrated to 229 water-level measurements from 181 wells during three synoptic surveys (July 17, 1995; July 31, 1996; and October 24, 1996). A quantifiable understanding of ground-water flow through the surficial aquifer was needed to evaluate remedial-action alternatives under consideration by the Naval Station Mayport to control the possible movement of contaminants from sites on the station. Multi-well aquifer tests, single-well tests, and slug tests were conducted to estimate the hydraulic properties of the surficial aquifer system, which was divided into three geohydrologic units?an S-zone and an I-zone separated by a marsh-muck confining unit. The recharge rate was estimated to range from 4 to 15 inches per year (95 percent confidence limits), based on a chloride-ratio method. Most of the simulations following model calibration were based on a recharge rate of 8 inches per year to unirrigated pervious areas. The advective displacement of saline pore water during the last 200 years was simulated using a particle-tracking routine, MODPATH, applied to calibrated steady-state and transient models of the Mayport peninsula. The surficial aquifer system at Naval Station Mayport has been modified greatly by natural and anthropogenic forces so that the freshwater flow system is expanding and saltwater is being flushed from the system. A new MODFLOW package (VAR1) was written to simulate the temporal variation of hydraulic properties caused by construction activities at Naval Station Mayport. The transiently simulated saltwater distribution after 200 years of displacement described the chloride distribution in the I-zone (determined from measurements made during 1993 and 1996) better than the steady-state simulation. The

ALCOHOL FLUSHING FOR REMOVING DNAPL'S FROM CLAY AND SAND LAYERED AQUIFER SYSTEMS

Energy Technology Data Exchange (ETDEWEB)

N.J. Hayden; P. Padgett; C. Farrell; J. Diebold; X. Zhou; M. Hood

1999-08-01

Alcohol flushing, also called cosolvent flushing, is a relatively new in-situ remediation technology that shows promise for removing organic solvents from the soil and groundwater. Soil and groundwater contamination from organic solvents and petroleum products is one of the most serious and widespread environmental problems of our time. Most of the DOE facilities and inactive sites are experiencing soil and groundwater contamination from organic solvents. These water immiscible solvents have entered the subsurface from leaking underground storage tanks and piping, and from past waste handling and disposal practices such as leaking lagoons, holding ponds and landfills. In many cases, they have traveled hundreds of feet down into the saturated zone. If left in the soil, these chemicals may pose a significant environmental and human health risk. Alcohol flushing has potential for application to spilled solvents located deep within the saturated zone which are difficult if not impossible to remove by current remediation strategies, thus, greatly expediting restoration time, reducing total remediation cost and reducing risk.

Alternative Solvents through Green Chemistry Project

Science.gov (United States)

Hintze, Paul E.; Quinn, Jacqueline

2014-01-01

Components in the aerospace industry must perform with accuracy and precision under extreme conditions, and surface contamination can be detrimental to the desired performance, especially in cases when the components come into contact with strong oxidizers such as liquid oxygen. Therefore, precision cleaning is an important part of a components preparation prior to utilization in aerospace applications. Current cleaning technologies employ a variety of cleaning agents, many of which are halogenated solvents that are either toxic or cause environmental damage. Thus, this project seeks to identify alternative precision cleaning solvents and technologies, including use of less harmful cleaning solvents, ultrasonic and megasonic agitation, low-pressure plasma cleaning techniques, and supercritical carbon dioxide extraction. Please review all data content found in the Public Data tab located at: https:techport.nasa.govview11697public

Sources, migration and transformation of antimony contamination in the water environment of Xikuangshan, China: Evidence from geochemical and stable isotope (S, Sr) signatures

Energy Technology Data Exchange (ETDEWEB)

Wen, Bing [Geological Survey, China University of Geosciences (Wuhan), Lumo Rd 388, Wuhan 430074, Hubei (China); State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences (Wuhan), Lumo Rd 388, Wuhan 430074, Hubei (China); Zhou, Jianwei, E-mail: jw.zhou@cug.edu.cn [School of Environmental Studies, China University of Geosciences (Wuhan), Lumo Rd 388, Wuhan 430074, Hubei (China); Zhou, Aiguo; Liu, Cunfu [School of Environmental Studies, China University of Geosciences (Wuhan), Lumo Rd 388, Wuhan 430074, Hubei (China); Xie, Lina [School of Environmental Studies, China University of Geosciences (Wuhan), Lumo Rd 388, Wuhan 430074, Hubei (China); State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences (Wuhan), Lumo Rd 388, Wuhan 430074, Hubei (China)

2016-11-01

The Xikuangshan (XKS) mine in central China is the largest antimony (Sb) mine in the world. The mining activity has seriously contaminated the waters in the area. To determine the sources, migration and transformation of Sb contamination, 32 samples from groundwater (aquifer water), surface water and mine water were collected for water chemistry, trace element and S{sub SO4} and Sr stable isotope analyses. The results showed that the groundwater and surface water were in an oxidized environment. The S{sub SO4} and Sr isotope compositions in the water indicated that dissolved Sb and SO{sub 4}{sup 2} originated from sulfide mineral (Sb{sub 2}S{sub 3}) oxidation, whereas radiogenic Sr may have been sourced from silicified limestone and stibnite in the Shetianqiao aquifer. Furthermore, a positive correlation between δ{sup 34}S{sub SO4} and δ{sup 87}Sr values revealed that the Sr, S and Sb in the waters had a common contamination source, i.e., silicified limestone and stibnite, whereas the Sr, S and Sb in rock and ore were sourced from Proterozoic basement clastics. The analysis also indicated that the isotope composition of dissolved SO{sub 4}{sup 2} {sup −} had been influenced by slight bacterial SO{sub 4} reduction in the Magunao aquifer. Mining or rock collapse may have caused Shetianqiao aquifer water to contaminate the Magunao aquifer water via mixing. This study has demonstrated that the stable isotopes of {sup 34}S{sub SO4} and {sup 87}Sr, combined with hydrochemical methods, are effective in tracking the sources, migration and transformation of Sb contamination. - Highlights: • Mining activities at XKS mine have caused serious water contamination. • The characteristics of Sb contamination in water environment are still unclear. • Combine S isotopes of sulfate and Sr isotopes with hydrochemical methods. • Sr, S, and Sb in natural water had a common source: silicified limestone and stibnite. • Shetianqiao aquifer water contaminated the Magunao

Sources, migration and transformation of antimony contamination in the water environment of Xikuangshan, China: Evidence from geochemical and stable isotope (S, Sr) signatures

International Nuclear Information System (INIS)

Wen, Bing; Zhou, Jianwei; Zhou, Aiguo; Liu, Cunfu; Xie, Lina

2016-01-01

The Xikuangshan (XKS) mine in central China is the largest antimony (Sb) mine in the world. The mining activity has seriously contaminated the waters in the area. To determine the sources, migration and transformation of Sb contamination, 32 samples from groundwater (aquifer water), surface water and mine water were collected for water chemistry, trace element and S_S_O_4 and Sr stable isotope analyses. The results showed that the groundwater and surface water were in an oxidized environment. The S_S_O_4 and Sr isotope compositions in the water indicated that dissolved Sb and SO_4"2 originated from sulfide mineral (Sb_2S_3) oxidation, whereas radiogenic Sr may have been sourced from silicified limestone and stibnite in the Shetianqiao aquifer. Furthermore, a positive correlation between δ"3"4S_S_O_4 and δ"8"7Sr values revealed that the Sr, S and Sb in the waters had a common contamination source, i.e., silicified limestone and stibnite, whereas the Sr, S and Sb in rock and ore were sourced from Proterozoic basement clastics. The analysis also indicated that the isotope composition of dissolved SO_4"2 "− had been influenced by slight bacterial SO_4 reduction in the Magunao aquifer. Mining or rock collapse may have caused Shetianqiao aquifer water to contaminate the Magunao aquifer water via mixing. This study has demonstrated that the stable isotopes of "3"4S_S_O_4 and "8"7Sr, combined with hydrochemical methods, are effective in tracking the sources, migration and transformation of Sb contamination. - Highlights: • Mining activities at XKS mine have caused serious water contamination. • The characteristics of Sb contamination in water environment are still unclear. • Combine S isotopes of sulfate and Sr isotopes with hydrochemical methods. • Sr, S, and Sb in natural water had a common source: silicified limestone and stibnite. • Shetianqiao aquifer water contaminated the Magunao aquifer water via mixing.

Seasonal Hydrologic Controls on Uranium and Iron Biogeochemistry in a Riparian Aquifer

Science.gov (United States)

Wilkins, M.; Williams, K. H.; Danczak, R. E.; Yabusaki, S.; Fang, Y.; Hobson, C.

2015-12-01

The maintenance of geochemically reducing conditions is generally optimal for the formation and preservation of reduced metals and mineral phases that can limit contaminant fate and transport. At a riparian aquifer near Rifle, CO, we tracked over six months the biogeochemical response within the aquifer to an annual pulse of dissolved oxygen (DO) that results from snowmelt-driven changes in Colorado River stage. In reduced portions of the aquifer (naturally reduced zones; NRZs) the re-oxidation of abundant iron sulfide minerals was the dominant oxygen-consuming process, and resulted in little DO intrusion into the deeper aquifer. In less reduced areas, DO intruded through the entire vertical profile of the aquifer. Across both regions, these perturbations resulted in changes to the microbial community structure, and aqueous metal pools. Two potentially different mechanisms of uranium mobilization were observed; (1) re-oxidation of reduced U(IV) phases in response to DO intrusion, and (2) mobilization of U(VI) from the vadose zone during water table rise. This high-resolution, long-term monitoring of aquifer biogeochemistry at the Rifle site has revealed dynamic microbial and geochemical responses to predictable, annual hydrologic perturbations, and offers an opportunity to further refine modeling approaches for such regions.

Origin of water salinity in the coastal Sarafand aquifer (South-Lebanon)

International Nuclear Information System (INIS)

Hashash, Adnan; Aranyossy, J.F.

1996-01-01

Author.The geochemical and isotopic study, based on the analysis of twenty water samples from well in the coastal plain of Sarafand (South-Lebanon), permit to eliminate the hypothesis of marine intrusion in this aquifer. The increase of salinity observed in certain wells is due to the contamination of cretaceous aquifer water by the quaternary formations. The two poles of mixing are respectively characterized: by weak tritium contents (between 2 and 3 UT) and a value of stable isotopes (-5,9<0,18<-5,5) corresponding to the appearance of cretaceous formation area; by the high tritium contents and enrichment relative to heavy isotope in the mineralized water of superficial formations. On the other hand, the isotope contents permit the set a rapid renewal of the cretaceous aquifer water due to quick circulation in the Karstic system

Some new hydraulic and tracer measurement techniques for heterogeneous aquifer formations

International Nuclear Information System (INIS)

Ptak, T.; Teutsch, G.

1990-01-01

Groundwater contamination assessment and remediation activities demand reliable techniques for the determination of the governing aquifer parameters and their spatial distribution. In order to define guidelines and recommendations, some existing underground investigation techniques were tested and new methods have been developed as a part of the research program at the Horkheimer Insel experimental field site. In this paper, some new developed field and laboratory techniques are introduced and the results compared for two example monitoring wells located in the northern part of the field site. It is shown that highly conductive and highly heterogeneous aquifers demand high resolution investigation techniques. For transport predictions, new methods are needed that are able to detect preferential flow paths. Results from multilevel tracer tests show that simple analytical interpretations are not valid for this type of aquifer. (Author) (8 refs., 12 figs., tab.)

ANALYSIS OF DISSOLVED METHANE, ETHANE, AND ETHYLENE IN GROUND WATER BY A STANDARD GAS CHROMATOGRAPHIC TECHNIQUE

Science.gov (United States)

The measurement of dissolved gases such as methane, ethane, and ethylene in ground water is important in determining whether intrinsic bioremediation is occurring in a fuel- or solvent-contaminated aquifer. A simple procedure is described for the collection and subsequent analys...

Application of a numerical model in the interpretation of a leaky aquifer test

International Nuclear Information System (INIS)

Schroth, B.; Narasimhan, T.N.

1997-01-01

The potential use of numerical models in aquifer analysis is by no means a new concept; yet relatively few engineers and scientists are taking advantage of this powerful tool that is more convenient to use now than ever before. In this technical note the authors present an example of using a numerical model in an integrated analysis of data from a three-layer leaky aquifer system involving well-bore storage, skin effects, variable discharge, and observation wells in the pumped aquifer and in an unpumped aquifer. The modeling detail may differ for other cases. The intent is to show that interpretation can be achieved with reduced bias by reducing assumptions in regard to system geometry, flow rate, and other details. A multiwell aquifer test was carried out at a site on the western part of the Lawrence Livermore National Laboratory (LLNL), located about 60 kilometers east of San Francisco. The test was conducted to hydraulically characterize one part of the site and thus help develop remediation strategies to alleviate the ground-water contamination

Optimizing Managed Aquifer Recharge (MAR) Systems for Removal of Trace Organic Chemicals (TOrCs)

KAUST Repository

Alidina, Mazahirali

2014-01-01

Managed aquifer recharge (MAR) is a low-energy subsurface water treatment system with the potential of being an important component of sustainable water reuse schemes. Alongside common wastewater contaminants, MAR systems have been shown

Technology summary of the in situ bioremediation demonstration (methane biostimulation) via horizontal wells at the Savannah River Site Integrated Demonstration Project

International Nuclear Information System (INIS)

Hazen, T.C.; Looney, B.B.; Fliermans, C.B.; Eddy-Dilek, C.A.; Lombard, K.H.; Enzien, M.V.; Dougherty, J.M.; Wear, J.

1994-01-01

The US Department of Energy, Office of Technology Development, has been sponsoring full-scale environmental restoration technology demonstrations for the past 4 years. The Savannah River Site Integrated Demonstration focuses on ''Clean-up of Soils ad Groundwater Contaminated with Chlorinated VOCs.'' Several laboratories including our own had demonstrated the ability of methanotrophic bacteria to completely degrade or mineralize chlorinated solvents, and these bacteria were naturally found in soil and aquifer material. Thus the test consisted of injection of methane mixed with air into the contaminated aquifer via a horizontal well and extraction from the vadose zone via a parallel horizontal well

Hydrostratigraphy, soil/sediment chemistry, and water quality, Potomac-Raritan-Magothy aquifer system, Puchack Well Field Superfund site and vicinity, Pennsauken Township, Camden County, New Jersey, 1997-2001

Science.gov (United States)

Barringer, Julia L.; Walker, Richard L.; Jacobsen, Eric; Jankowski, Pamela

2010-01-01

Drinking-water supplies from the Potomac-Raritan-Magothy aquifer system at the Puchack well field in Pennsauken Township, Camden County, New Jersey, have been contaminated by hexavalent chromium-the most toxic and mobile form-at concentrations exceeding the New Jersey maximum contaminant level of 100 micrograms per liter. Also, scattered but widespread instances of volatile organic compounds (primarily trichloroethylene) at concentrations that exceed their respective maximum contaminant levels in the area's ground water have been reported. Because inorganic and organic contaminants are present in the ground water underlying the Puchack well field, no water from there has been withdrawn for public supply since 1998, when the U.S. Environmental Protection Agency (USEPA) added the area that contains the Puchack well field to the National Priorities List. As part of the USEPA's investigation of the Puchack Well Field Superfund site, the U.S. Geological Survey (USGS) conducted a study during 1997-2001 to (1) refine previous interpretations of the hydrostratigraphic framework, hydraulic gradients, and local directions of ground-water flow; (2) describe the chemistry of soils and saturated aquifer sediments; and (3) document the quality of ground water in the Potomac-Raritan-Magothy aquifer system in the area. The four major water-bearing units of the Potomac-Raritan-Magothy aquifer system-the Upper aquifer (mostly unsaturated in the study area), the Middle aquifer, the Intermediate Sand (a local but important unit), and the Lower aquifer-are separated by confining units. The confining units contain areas of cut and fill, resulting in permeable zones that permit water to pass through them. Pumping from the Puchack well field during the past 3 decades resulted in downward hydraulic gradients that moved contaminants into the Lower aquifer, in which the production wells are finished, and caused ground water to flow northeast, locally. A comparison of current (1997

Solvent extraction for remediation of manufactured gas plant sites

International Nuclear Information System (INIS)

Luthy, R.G.; Dzombak, D.A.; Peters, C.; Ali, M.A.; Roy, S.B.

1992-12-01

This report presents the results of an initial assessment of the feasibility of solvent extraction for removing coal tar from the subsurface or for treating contaminated soil excavated at manufactured gas plant (MGP) sites. In situ solvent extraction would involve injection, recovery, and reclamation for reinjection of an environmentally-benign, water-miscible solvent. Accelerated dissolution and removal of coaltar from the subsurface might be desirable as a remedial approach if excavation is not practical (e.g., the site underlies facilities in current use), direct pumping of coal tar is ineffective, and bioremediation is not feasible because of the presence of high concentrations of coal tar. Both laboratory experiments and engineering evaluations were performed to provide a basis for the initial feasibility assessment. Laboratory work included identification and evaluation of promising solvents, measurement of fundamental properties of coal tar-solvent-water systems, and measurement of rates of dissolution of coal tar in porous media into flowing solvent-water solutions. Engineering evaluations involved identification of common hydrogeologic features and contaminant distributions at MGP sites, and identification and evaluation of possible injection-recovery well deployment schemes. A coupled flow-chemistry model was developed for simulation of the in situ process and evaluation of the well deployment schemes. Results indicate that in situsolvent extraction may be able to recover a significant amount of coal tar from the subsurface within a reasonable time frame (on the order of one year or so) provided that subsurface conditions are conducive to process implementation. Some important implementation issues remain to be addressed

Study of the inter-relation between shallow and deep aquifers in Mardan Valley, Pakistan

International Nuclear Information System (INIS)

Ishaq Sajjad, M.

1987-04-01

This study concerns the determination of the relationship between shallow and deep aquifers in the Mardan Valley, in Pakistan. The environmental isotopes, 18 O, 2 H, 3 H, 14 C and 13 C were used in conjunction with classical hydrogeological methods to determine the origins of the different groundwaters in the valley. The irrigation water contributes significantly to the water logging of the study area. There is also the evidence of upward leakage from the deep groundwater system which contributes to this effect. There is no evidence of contamination of the deep aquifers as the quality is good. Groundwater movement in the deep aquifer is slow in the order of tens of years

Development of a three-dimensional ground-water model of the Hanford Site unconfined aquifer system: FY 1995 status report

International Nuclear Information System (INIS)

Wurstner, S.K.; Thorne, P.D.; Chamness, M.A.; Freshley, M.D.; Williams, M.D.

1995-12-01

A three-dimensional numerical model of ground-water flow was developed for the uppermost unconfined aquifer at the Hanford Site in south-central Washington. Development of the model is supported by the Hanford Site Ground-Water Surveillance Project, managed by the Pacific Northwest National Laboratory, which is responsible for monitoring the sitewide movement of contaminants in ground water beneath the Hanford Site. Two objectives of the Ground-Water Surveillance Project are to (1) identify and quantify existing, emerging, or potential ground-water quality problems, and (2) assess the potential for contaminants to migrate from the Hanford Site through the ground-water pathway. Numerical models of the ground-water flow system are important tools for estimating future aquifer conditions and predicting the movement of contaminants through ground water. The Ground-Water Surveillance Project has supported development and maintenance of a two-dimensional model of the unconfined aquifer. This report describes upgrade of the two-dimensional model to a three-dimensional model. The numerical model is based on a three-dimensional conceptual model that will be continually refined and updated as additional information becomes available. This report presents a description of the three-dimensional conceptual model of ground-water flow in the unconfined aquifer system and then discusses the cur-rent state of the three-dimensional numerical model

Carbonate aquifers

Science.gov (United States)

Cunningham, Kevin J.; Sukop, Michael; Curran, H. Allen

2012-01-01

Only limited hydrogeological research has been conducted using ichnology in carbonate aquifer characterization. Regardless, important applications of ichnology to carbonate aquifer characterization include its use to distinguish and delineate depositional cycles, correlate mappable biogenically altered surfaces, identify zones of preferential groundwater flow and paleogroundwater flow, and better understand the origin of ichnofabric-related karst features. Three case studies, which include Pleistocene carbonate rocks of the Biscayne aquifer in southern Florida and Cretaceous carbonate strata of the Edwards–Trinity aquifer system in central Texas, demonstrate that (1) there can be a strong relation between ichnofabrics and groundwater flow in carbonate aquifers and (2) ichnology can offer a useful methodology for carbonate aquifer characterization. In these examples, zones of extremely permeable, ichnofabric-related macroporosity are mappable stratiform geobodies and as such can be represented in groundwater flow and transport simulations.

Aquifer geochemistry at potential aquifer storage and recovery sites in coastal plain aquifers in the New York city area, USA

Science.gov (United States)

Brown, C.J.; Misut, P.E.

2010-01-01

The effects of injecting oxic water from the New York city (NYC) drinking-water supply and distribution system into a nearby anoxic coastal plain aquifer for later recovery during periods of water shortage (aquifer storage and recovery, or ASR) were simulated by a 3-dimensional, reactive-solute transport model. The Cretaceous aquifer system in the NYC area of New York and New Jersey, USA contains pyrite, goethite, locally occurring siderite, lignite, and locally varying amounts of dissolved Fe and salinity. Sediment from cores drilled on Staten Island and western Long Island had high extractable concentrations of Fe, Mn, and acid volatile sulfides (AVS) plus chromium-reducible sulfides (CRS) and low concentrations of As, Pb, Cd, Cr, Cu and U. Similarly, water samples from the Lloyd aquifer (Cretaceous) in western Long Island generally contained high concentrations of Fe and Mn and low concentrations of other trace elements such as As, Pb, Cd, Cr, Cu and U, all of which were below US Environmental Protection Agency (USEPA) and NY maximum contaminant levels (MCLs). In such aquifer settings, ASR operations can be complicated by the oxidative dissolution of pyrite, low pH, and high concentrations of dissolved Fe in extracted water.The simulated injection of buffered, oxic city water into a hypothetical ASR well increased the hydraulic head at the well, displaced the ambient groundwater, and formed a spheroid of injected water with lower concentrations of Fe, Mn and major ions in water surrounding the ASR well, than in ambient water. Both the dissolved O2 concentrations and the pH of water near the well generally increased in magnitude during the simulated 5-a injection phase. The resultant oxidation of Fe2+ and attendant precipitation of goethite during injection provided a substrate for sorption of dissolved Fe during the 8-a extraction phase. The baseline scenario with a low (0.001M) concentration of pyrite in aquifer sediments, indicated that nearly 190% more water

Extent and severity of groundwater contamination based on hydrochemistry mechanism of sandy tropical coastal aquifer.

Science.gov (United States)

Isa, Noorain Mohd; Aris, Ahmad Zaharin; Sulaiman, Wan Nor Azmin Wan

2012-11-01

Small islands are susceptible to anthropogenic and natural activities, especially in respect of their freshwater supply. The freshwater supply in small islands may be threatened by the encroachment of seawater into freshwater aquifers, usually caused by over pumping. This study focused on the hydrochemistry of the Kapas Island aquifer, which controls the groundwater composition. Groundwater samples were taken from six constructed boreholes for the analysis and measurement of its in-situ and major ions. The experimental results show a positive and significant correlation between Na-Cl (r=0.907; paquifer bedrock. About 76% of collected data (n=108) were found to be in the dissolution process of carbonate minerals. Moreover, the correlation between total CEC and Ca shows a positive and strong relationship (r=0.995; pchemical composition. The output of this research explains the chemical mechanism attributed to the groundwater condition of the Kapas Island aquifer. Copyright © 2012 Elsevier B.V. All rights reserved.

Use of static Quantitative Microbial Risk Assessment to determine pathogen risks in an unconfined carbonate aquifer used for Managed Aquifer Recharge.

Science.gov (United States)

Toze, Simon; Bekele, Elise; Page, Declan; Sidhu, Jatinder; Shackleton, Mark

2010-02-01

Managed Aquifer Recharge (MAR) is becoming a mechanism used for recycling treated wastewater and captured urban stormwater and is being used as a treatment barrier to remove contaminants such as pathogens from the recharged water. There is still a need, however, to demonstrate the effectiveness of MAR to reduce any residual risk of pathogens in the recovered water. A MAR research site recharging secondary treated wastewater in an unconfined carbonate aquifer was used in conjunction with a static Quantitative Microbial Risk Assessment (QMRA) to assess the microbial pathogen risk in the recovered water following infiltration and aquifer passage. The research involved undertaking a detailed hydrogeological assessment of the aquifer at the MAR site and determining the decay rates of reference pathogens from an in-situ decay study. These variables along with literature data were then used in the static QMRA which demonstrated that the recovered water at this site did not meet the Australian Guidelines for recycled water when used for differing private green space irrigation scenarios. The results also confirmed the importance of obtaining local hydrogeological data as local heterogeneity can influence of residence time in the aquifer which, in turn, influences the outcomes. The research demonstrated that a static QMRA can be used to determine the residual risk from pathogens in recovered water and showed that it can be a valuable tool in the preliminary design and operation of MAR systems and the incorporation of complementary engineered treatment processes to ensure that there is acceptable health risk from the recovered water. Crown Copyright 2009. Published by Elsevier Ltd. All rights reserved.

In situ treatment of arsenic contaminated groundwater by aquifer iron coating: Experimental study.

Science.gov (United States)

Xie, Xianjun; Wang, Yanxin; Pi, Kunfu; Liu, Chongxuan; Li, Junxia; Liu, Yaqing; Wang, Zhiqiang; Duan, Mengyu

2015-09-15

In situ arsenic removal from groundwater by an aquifer iron coating method has great potential to be a cost effective and simple groundwater remediation technology, especially in rural and remote areas where groundwater is used as the main water source for drinking. The in situ arsenic removal technology was first optimized by simulating arsenic removal in various quartz sand columns under anoxic conditions. The effectiveness was then evaluated in an actual high-arsenic groundwater environment. The arsenic removal mechanism by the coated iron oxide/hydroxide was investigated under different conditions using scanning electron microscopy (SEM)/X-ray absorption spectroscopy, electron probe microanalysis, and Fourier transformation infrared spectroscopy. Aquifer iron coating method was developed via a 4-step alternating injection of oxidant, iron salt and oxygen-free water. A continuous injection of 5.0 mmol/L FeSO4 and 2.5 mmol/L NaClO for 96 h can form a uniform goethite coating on the surface of quartz sand without causing clogging. At a flow rate of 7.2 mL/min of the injection reagents, arsenic (as Na2HAsO4) and tracer fluorescein sodium to pass through the iron-coated quartz sand column were approximately at 126 and 7 column pore volumes, respectively. The retardation factor of arsenic was 23.0, and the adsorption capacity was 0.11 mol As per mol Fe. In situ arsenic removal from groundwater in an aquifer was achieved by simultaneous injections of As(V) and Fe(II) reagents. Arsenic fixation resulted from a process of adsorption/co-precipitation with fine goethite particles by way of bidentate binuclear complexes. Therefore, the study results indicate that the high arsenic removal efficiency of the in situ aquifer iron coating technology likely resulted from the expanded specific surface area of the small goethite particles, which enhanced arsenic sorption capability and/or from co-precipitation of arsenic on the surface of goethite particles. Copyright © 2015

Distribution and composition of microbial populations in a landfill leachate contaminated aquifer (Grindsted, Denmark)

DEFF Research Database (Denmark)

Ludvigsen, L.; Albrechtsen, H.-J.; Ringelberg, D.

1999-01-01

To investigate whether landfill leachates affected the microbial biomass and/or community composition of the extant microbiota, 37 samples were collected along a 305-m transect of a shallow landfill-leachate polluted aquifer. The samples were analyzed for total numbers of bacteria by use of the a......To investigate whether landfill leachates affected the microbial biomass and/or community composition of the extant microbiota, 37 samples were collected along a 305-m transect of a shallow landfill-leachate polluted aquifer. The samples were analyzed for total numbers of bacteria by use...... of the acridine orange direct count method (AODC). Numbers of dominant, specific groups of bacteria and total numbers of protozoa were measured by use of the most probable number method (MPN). Viable biomass estimates were obtained from measures of ATP and ester-linked phospholipid fatty acid (PLFA......) concentrations. The estimated numbers of total bacteria by direct counts were relatively constant throughout the aquifer, ranging from a low of 4.8 × 106 cells/g dry weight (dw) to a high of 5.3 × 107 cells/g dw. Viable biomass estimates based on PLFA concentrations were one to three orders of magnitude lower...

Edible Oil Barriers for Treatment of Chlorinated Solvent and Perchlorate-Contaminated Groundwater

Science.gov (United States)

2010-02-01

The groundwater potentiometric surface beneath SWMU 17 is relatively flat with some tidal influence resulting in fluctuating groundwater flow...after its application, the pH within most of the aquifer would be expected to vary between background (~5) and 9. A titration experiment determined

Abiotic Removal of TCE and cis-DCE by Magnetite under Aerobic Conditions in Ground Water (Maryland)

Science.gov (United States)

The former Twin Cities Army Ammunition Plant (TCAAP) is located just north of St. Paul, Minnesota. Disposal of chlorinated solvents at the Building102 site on the TCAAP contaminated groundwater in the shallow, unconsolidated sand aquifer with TCE and cis-DCE. Concentrations of ...

The integrated impacts of natural processes and human activities on the origin and processes of groundwater salinization in the coastal aquifers of Beihai, Southern China

Science.gov (United States)

Li, Q.; Zhan, Y., , Dr; Chen, W. Ms; Yu, S., , Dr

2017-12-01

Salinization in coastal aquifers usually is the results of contamination related to both seawater intrusion and water-rock interaction. The chemical and isotopic methods were combined to identify the origin and processes of groundwater salinization in Daguansha area of Beihai. The concentrations of the major ions that dominate in sea water (Cl-, Na+, Ca2+, Mg2+ and SO2- 4), as well as the isotopic ratios (2H, 18O, 87Sr/86Sr and 13C) suggest that the salinization occurring in the aquifer water of the coastal plain is related to seawater and the prevailing hydrochemical processes are evaporation, mixing, dissolution and ion exchange. For the unconfined aquifer, groundwater salinization occurred in parts of the area, which is significantly influenced by the land-based sea farming. The integrated impacts of seawater intrusion from the Beibuwan Gulf and infiltration of seawater from the culture ponds is identified in the confined aquifer I at site BBW2. In consequence, the leakage from this polluted aquifer causes the salinization of groundwater in the confined aquifer II. At site BBW3, the confined aquifer I and lower confined aquifer II are remarkably contaminated by seawater intrusion. The weak connectivity with upper aquifers and seaward movement of freshwater prevents saltwater from encroaching the confined aquifer III. Above all, understanding of the origin and processes of groundwater salinization will provide essential information for sustainable planning and management of groundwater resources in this region.

Multi-scale nitrate transport in a sandstone aquifer system under intensive agriculture

Science.gov (United States)

Paradis, Daniel; Ballard, Jean-Marc; Lefebvre, René; Savard, Martine M.

2018-03-01

Nitrate transport in heterogeneous bedrock aquifers is influenced by mechanisms that operate at different spatial and temporal scales. To understand these mechanisms in a fractured sandstone aquifer with high porosity, a groundwater-flow and nitrate transport model—reproducing multiple hydraulic and chemical targets—was developed to explain the actual nitrate contamination observed in groundwater and surface water in a study area on Prince Edward Island, Canada. Simulations show that nitrate is leached to the aquifer year-round, with 61% coming from untransformed and transformed organic sources originating from fertilizers and manure. This nitrate reaches the more permeable shallow aquifer through fractures in weathered sandstone that represent only 1% of the total porosity (17%). Some of the nitrate reaches the underlying aquifer, which is less active in terms of groundwater flow, but most of it is drained to the main river. The river-water quality is controlled by the nitrate input from the shallow aquifer. Groundwater in the underlying aquifer, which has long residence times, is also largely influenced by the diffusion of nitrate in the porous sandstone matrix. Consequently, following a change of fertilizer application practices, water quality in domestic wells and the river would change rapidly due to the level of nitrate found in fractures, but a lag time of up to 20 years would be necessary to reach a steady level due to diffusion. This demonstrates the importance of understanding nitrate transport mechanisms when designing effective agricultural and water management plans to improve water quality.

Simulation–optimization model for groundwater contamination ...

Indian Academy of Sciences (India)

used techniques for groundwater remediation in which the contaminated groundwater is pumped ... ing the affected groundwater aquifer down to some drinking water standard. Several .... For simplicity, rectangular support domain is used in this study. Figure 1 ..... For PAT remediation system, decision variables include the.

Mercury (II) reduction and co-precipitation of metallic mercury on hydrous ferric oxide in contaminated groundwater.

Science.gov (United States)

Richard, Jan-Helge; Bischoff, Cornelia; Ahrens, Christian G M; Biester, Harald

2016-01-01

Mercury (Hg) speciation and sorption analyses in contaminated aquifers are useful for understanding transformation, retention, and mobility of Hg in groundwater. In most aquifers hydrous ferric oxides (HFOs) are among the most important sorbents for trace metals; however, their role in sorption or mobilization of Hg in aquifers has been rarely analyzed. In this study, we investigated Hg chemistry and Hg sorption to HFO under changing redox conditions in a highly HgCl2-contaminated aquifer (up to 870μgL(-1) Hg). Results from aqueous and solid phase Hg measurements were compared to modeled (PHREEQC) data. Speciation analyses of dissolved mercury indicated that Hg(II) forms were reduced to Hg(0) under anoxic conditions, and adsorbed to or co-precipitated with HFO. Solid phase Hg thermo-desorption measurements revealed that between 55 and 93% of Hg bound to HFO was elemental Hg (Hg(0)). Hg concentrations in precipitates reached more than 4 weight %, up to 7000 times higher than predicted by geochemical models that do not consider unspecific sorption to and co-precipitation of elemental Hg with HFO. The observed process of Hg(II) reduction and Hg(0) formation, and its retention and co-precipitation by HFO is thought to be crucial in HgCl2-contaminated aquifers with variable redox-conditions regarding the related decrease in Hg solubility (factor of ~10(6)), and retention of Hg in the aquifer. Copyright © 2015 Elsevier B.V. All rights reserved.

Alternative Solvents and Technologies for Precision Cleaning of Aerospace Components

Science.gov (United States)

Grandelli, Heather; Maloney, Phillip; DeVor, Robert; Hintze, Paul

2014-01-01

Precision cleaning solvents for aerospace components and oxygen fuel systems, including currently used Vertrel-MCA, have a negative environmental legacy, high global warming potential, and have polluted cleaning sites. Thus, alternative solvents and technologies are being investigated with the aim of achieving precision contamination levels of less than 1 mg/sq ft. The technologies being evaluated are ultrasonic bath cleaning, plasma cleaning and supercritical carbon dioxide cleaning.

Investigation of shallow groundwater contamination near East Fork Poplar Creek, Oak Ridge, Tennessee

International Nuclear Information System (INIS)

Carmichael, J.K.

1989-01-01

Alluvial soils of the flood plain of East Fork Poplar Creek in Oak Ridge, Tennessee, are contaminated with mercury and other metals, organic compounds, and radionuclides originating from the Y-12 Plant, a nuclear-processing facility located within the US Department of Energy's Oak Ridge Reservation. Observation wells were installed in the shallow aquifer of the flood plain, and water quality samples were collected to determine if contaminants are present in the shallow groundwater. Groundwater in the shallow aquifer occurs under water-table conditions. Recharge is primarily from precipitation and discharge is to East Fork Poplar Creek. Groundwater levels fluctuate seasonally in response to variations in recharge and evapotranspiration. During extremely dry periods, the water table drops below the base of the shallow aquifer in some flood-plain areas. Contaminants were found in water samples from several of the wells in concentrations which equaled or exceeded drinking-water standards established by the US Environmental Protection Agency are antimony, chromium, lead, mercury, selenium, phenols, and strontium-90. Total and dissolved uranium concentrations exceeded the analytical detection limit in nearly 70% of the wells in the flood plain. The results of water quality determinations demonstrate that elevated concentrations of most trace metals (and possibly organic compounds and radionuclides) were caused by contaminated sediments in the samples. The presence of contaminated sediment in samples is suspected to be the result of borehole contamination during well installation. 21 refs., 20 figs., 6 tabs

Enhanced bioremediation as a cost effective approach following thermally enhanced soil vapour extraction for sites requiring remediation of chlorinated solvents - 16296

International Nuclear Information System (INIS)

Kozlowska, Anna-Maria; Kahlon, Manjit S.; Langford, Steve R.; Williams, Haydn G.

2009-01-01

Thermally enhanced bioremediation can be a more cost-effective alternative to full scale in-situ thermal treatment especially for sites contaminated with chlorinated solvents, where reductive dechlorination is or might be a dominant biological step. The effect of Thermally Enhanced Soil Vapour Extraction (TESVE) on indigenous microbial communities and the potential for subsequent biological polishing of chlorinated solvents was investigated in field trials at the Western Storage Area (WSA) - RSRL (formerly United Kingdom Atomic Energy Authority - UKAEA) Oxfordshire, UK. The WSA site had been contaminated with various chemicals including mineral oil, chloroform, trichloroethane (TCA), carbon tetrachloride and tetrachloroethene (PCE). The contamination had affected the unsaturated zone, groundwater in the chalk aquifer and was a continuing source of groundwater contamination below the WSA. During TESVE the target treatment zone was heated to above the boiling point of water increasing the degree of volatilization of contaminants of concern (CoC), which were mobilised and extracted in the vapour phase. A significant reduction of concentrations of chlorinated solvent in the unsaturated zone was achieved by the full-scale application of TESVE - In Situ Thermal Desorption (ISTD) technology. The rock mass temperature within target treatment zone remained in the range of 35 deg. - 44 deg. C, 6 months after cessation of heating. The concentration of chlorinated ethenes and other CoC were found to be significantly lower adjacent to the thermal treatment area and 1 to 2 orders of magnitude lower within the thermal treatment zone. Samples were collected within and outside the thermal treatment zone using BioTraps R (passive, in- situ microbial samplers) from which the numbers of specific bacteria were measured using quantitative polymerase chain reaction (qPCR) methods of analysis. High populations of reductive de-chlorinators such as Dechalococcoides spp. and Dehalobacter spp

300 area solvent evaporator interim status closure plan: Revision 2

International Nuclear Information System (INIS)

1989-02-01

This document describes activities for the closure of a hazardous waste tank treatment facility operated by the US Department of Energy-Richland Operations Office (DOE-RL) and co-operated by the Westinghouse Hanford Company (WHC). This treatment facility was a solvent evaporator located in the 300 Area of the Hanford Site, from 1975 to 1985 on behalf of DOE-RL. The 300 Area Solvent Evaporator (300 ASE) was a modified load lugger (dumpster) in which solvent wastes were evaporated. Some of the solvents were radioactively contaminated because they came from a degreaser which processed bare uranium metal billets from the N Reactor Fuel Manufacturing Facility. The waste was composed of perchloroethylene, trichloroethylene, 1,1,1-trichloroethane, ethyl acetate/bromine solution, paint shop solvents and possibly some used oil. Also, small amounts of uranium, copper, zirconium and possibly beryllium were present in the degreaser solvents as particulates. Radioactive and non-radioactive solvents were not segregated in the 300 ASE, and the entire mixture was regarded as mixed waste

Superfund Record of Decision (EPA Region 5): Ossineke Groundwater Contamination Site, Alpena County, Ossineke, MI. (First remedial action), June 1991. Final report

International Nuclear Information System (INIS)

1991-01-01

The Ossineke Ground Water Contamination site is an area overlying a contaminated aquifer in Ossineke, Alpena County, Michigan. The site hydrogeology is characterized by an upper aquifer and lower confined aquifer, both of which supply drinking water to local residents. Historically there have been two contaminant source areas of concern within Ossineke. Area 1 is in the center of the Town of Ossineke where two gas stations are located, consisting of underground storage tanks, and a former automobile rustproofing shop. Area 2 is a laundry and dry cleaning facility that has an associated wash water pond containing chlorinated hydrocarbons and VOCs. The State advised all users of the upper aquifer to stop using their wells. In 1982, the State discovered that a snow plow had hit a gasoline pump causing an unknown amount of gasoline to spill and, subsequently, contaminate the basements of several businesses. In 1986, the State replaced residential wells affected by ground water contamination. Because the contaminants of concern have been confirmed to be related to petroleum releases from underground storage tanks, the Superfund program does not have the authority to address cleanup under CERLCLA. The selected remedial action for the site is that no further action

Hydrogen peroxide treatment of TCE contaminated soil

International Nuclear Information System (INIS)

Hurst, D.H.; Robinson, K.G.; Siegrist, R.L.

1993-01-01

Solvent contaminated soils are ubiquitous in the industrial world and represent a significant environmental hazard due to their persistence and potentially negative impacts on human health and the environment. Environmental regulations favor treatment of soils with options which reduce the volume and toxicity of contaminants in place. One such treatment option is the in-situ application of hydrogen peroxide to soils contaminated with chlorinated solvents such as trichloroethylene (TCE). This study investigated hydrogen peroxide mass loading rates on removal of TCE from soils of varying organic matter content. Batch experiments conducted on contaminated loam samples using GC headspace analysis showed up to 80% TCE removal upon peroxide treatment. Column experiments conducted on sandy loam soils with high organic matter content showed only 25% TCE removal, even at hydrogen peroxide additions of 25 g peroxide per kg soil

Constraints of costal aquifer functioning in a deeply antropized area through a multi-isotope fingerprinting (Recife, Brazil)

Science.gov (United States)

Petelet-Giraud, Emmanuelle; Cary, Lise; Bertrand, Guillaume; Hirata, Ricardo; Martins, Veridiana; Montenegro, Suzana; Pauwels, Hélène; Kloppmann, Wolfram; Aquilina, Luc

2014-05-01

The Metropolitan Region of Recife (RMR) went through large changes of water and land uses over the last decades due to an increasing demographic pressure (1.5 M of inhabitants). These evolutions gave rise to numerous environmental consequences, such as a dramatic decline of the water levels, groundwater salinization and contamination. This degradation of natural resources is linked to the increase of water demand that is also punctually amplified by drought periods, inducing the construction of thousands of private wells. Recife city was built on an estuarine area, at the geological limits of the two sedimentary basins of Pernambuco (north of the city) and Paraíba (south of the city) separated by a famous shear zone (the Pernambuco lineament). Tectonic and sedimentary events involved in the genesis and evolution of these basins were mainly controlled by the opening of the Atlantic Ocean leading to the deposition of cretaceous sediments which now constitute the two main exploited aquifers, the Beberibe and Cabo aquifers. These two deep aquiferous formations are topped by the unconfined Boa Viagem aquifer of quaternary sediments. It is the most directly exposed to contamination, since it is connected to mangroves, rivers, estuaries and highly urbanized areas. Both the Beberibe and Cabo aquifers contain large clay levels and are separated by a rather continuous clayed formation which seems to play a consistent role of screen and to interfere in the hydraulic connections between the three aquifers. Previous isotopic studies have shown that recharge processes are similar in the aquifers, suggesting that exchanges may occur and may be modified or amplified by overexploitation. This very complex aquifer system is studied through more than 60 water samples, including some surface water samples from the main rivers. A methodology based on multi-isotopes fingerprinting is applied, including stable isotopes of the water molecule, strontium isotopes, boron isotopes, sulfur

Maps of estimated nitrate and arsenic concentrations in basin-fill aquifers of the southwestern United States

Science.gov (United States)

Beisner, Kimberly R.; Anning, David W.; Paul, Angela P.; McKinney, Tim S.; Huntington, Jena M.; Bexfield, Laura M.; Thiros, Susan A.

2012-01-01

Human-health concerns and economic considerations associated with meeting drinking-water standards motivated a study of the vulnerability of basin-fill aquifers to nitrate contamination and arsenic enrichment in the southwestern United States. Statistical models were developed by using the random forest classifier algorithm to predict concentrations of nitrate and arsenic across a model grid representing about 190,600 square miles of basin-fill aquifers in parts of Arizona, California, Colorado, Nevada, New Mexico, and Utah. The statistical models, referred to as classifiers, reflect natural and human-related factors that affect aquifer vulnerability to contamination and relate nitrate and arsenic concentrations to explanatory variables representing local- and basin-scale measures of source and aquifer susceptibility conditions. Geochemical variables were not used in concentration predictions because they were not available for the entire study area. The models were calibrated to assess model accuracy on the basis of measured values.Only 2 percent of the area underlain by basin-fill aquifers in the study area was predicted to equal or exceed the U.S. Environmental Protection Agency drinking-water standard for nitrate as N (10 milligrams per liter), whereas 43 percent of the area was predicted to equal or exceed the standard for arsenic (10 micrograms per liter). Areas predicted to equal or exceed the drinking-water standard for nitrate include basins in central Arizona near Phoenix; the San Joaquin Valley, the Santa Ana Inland, and San Jacinto Basins of California; and the San Luis Valley of Colorado. Much of the area predicted to equal or exceed the drinking-water standard for arsenic is within a belt of basins along the western portion of the Basin and Range Physiographic Province that includes almost all of Nevada and parts of California and Arizona. Predicted nitrate and arsenic concentrations are substantially lower than the drinking-water standards in much of

Stimulation of reductive dechlorination of tetrachloroethane in anaerobic aquifer microcosms by addition of short-chain organic acids or alcohols

International Nuclear Information System (INIS)

Gibson, S.A.; Sewell, G.W.

1992-01-01

Although the ecological and public health risk associated with tetrachloroethene (PCE) contamination may be the most severe when spills affect groundwater, little is known about the environmental conditions necessary to initiate and sustain dehalogenation activity in contaminated aquifers. This study was done with core material collected from a site impacted by both aviation gasoline and chloroethenes at a Coast Guard Air Station at Traverse City, Michigan. The effect of the addition of common fermentation products on the dehalogenation of tetrachloroethene was studied in methanogenic slurries made with aquifer solids. Lactate, propionate, crotonate, butyrate, and ethanol stimulated dehalogenation activity, while acetate, methanol, and isopropanol did not

Coastal ground water at risk - Saltwater contamination at Brunswick, Georgia and Hilton Head Island, South Carolina

Science.gov (United States)

Krause, Richard E.; Clarke, John S.

2001-01-01

IntroductionSaltwater contamination is restricting the development of ground-water supply in coastal Georgia and adjacent parts of South Carolina and Florida. The principal source of water in the coastal area is the Upper Floridan aquifer—an extremely permeable and high-yielding aquifer—which was first developed in the late 1800s. Pumping from the aquifer has resulted in substantial ground-water-level decline and subsequent saltwater intrusion of the aquifer from underlying strata containing highly saline water at Brunswick, Georgia, and with encroachment of sea-water into the aquifer at the northern end of Hilton Head Island, South Carolina. The saltwater contamination at these locations has constrained further development of the Upper Floridan aquifer in the coastal area and has created competing demands for the limited supply of freshwater. The Georgia Department of Natural Resources, Georgia Environmental Protection Division (GaEPD) has restricted permitted withdrawal of water from the Upper Floridan aquifer in parts of the coastal area (including the Savannah and Brunswick areas) to 1997 rates, and also has restricted additional permitted pumpage in all 24 coastal area counties to 36 million gallons per day above 1997 rates. These actions have prompted interest in alternative management of the aquifer and in the development of supplemental sources of water supply including those from the shallower surficial and upper and lower Brunswick aquifers and from the deeper Lower Floridan aquifer.

3D Geospatial Models for Visualization and Analysis of Groundwater Contamination at a Nuclear Materials Processing Facility

Science.gov (United States)

Stirewalt, G. L.; Shepherd, J. C.

2003-12-01

Analysis of hydrostratigraphy and uranium and nitrate contamination in groundwater at a former nuclear materials processing facility in Oklahoma were undertaken employing 3-dimensional (3D) geospatial modeling software. Models constructed played an important role in the regulatory decision process of the U.S. Nuclear Regulatory Commission (NRC) because they enabled visualization of temporal variations in contaminant concentrations and plume geometry. Three aquifer systems occur at the site, comprised of water-bearing fractured shales separated by indurated sandstone aquitards. The uppermost terrace groundwater system (TGWS) aquifer is composed of terrace and alluvial deposits and a basal shale. The shallow groundwater system (SGWS) aquifer is made up of three shale units and two sandstones. It is separated from the overlying TGWS and underlying deep groundwater system (DGWS) aquifer by sandstone aquitards. Spills of nitric acid solutions containing uranium and radioactive decay products around the main processing building (MPB), leakage from storage ponds west of the MPB, and leaching of radioactive materials from discarded equipment and waste containers contaminated both the TGWS and SGWS aquifers during facility operation between 1970 and 1993. Constructing 3D geospatial property models for analysis of groundwater contamination at the site involved use of EarthVision (EV), a 3D geospatial modeling software developed by Dynamic Graphics, Inc. of Alameda, CA. A viable 3D geohydrologic framework model was initially constructed so property data could be spatially located relative to subsurface geohydrologic units. The framework model contained three hydrostratigraphic zones equivalent to the TGWS, SGWS, and DGWS aquifers in which groundwater samples were collected, separated by two sandstone aquitards. Groundwater data collected in the three aquifer systems since 1991 indicated high concentrations of uranium (>10,000 micrograms/liter) and nitrate (> 500 milligrams

First-principles prediction of liquid/liquid interfacial tension

DEFF Research Database (Denmark)

Andersson, Martin Peter; Bennetzen, M.V.; Klamt, A.

2014-01-01

of groundwater aquifers contaminated by chlorinated solvents to drug delivery and a host of industrial processes. Here, we present a model for predicting interfacial tension from first principles using density functional theory calculations. Our model requires no experimental input and is applicable to liquid...

Hydrogeological geochemical and isotopic study of the coastal aquifer of Sousse Eastern, Tunisia

International Nuclear Information System (INIS)

Ben-Hamouda, M. F.; Carreira, P.; Marques, J. M.; Eggenkamp, H.

2012-12-01

At Sahel, near one of the seaside resort available in Tunisia, the water quantity and quality is a major problem ever at southern center of Tunisia. The Oued Laya coastal system is no exception. The levels, a shallow aquifer up to depths of about 60 m whose reservoir is mainly formed by Mio-Pliocnesediments (with some gypsum lenses dispersed within the geological formations) and deep aquifer, situated between 100 and 250 m depth, located in the Miocene sandstone formations. The results of geochemical and isotopic studies have shown that groundwater salinity seems not be linked with the increasing water well's abstraction. In contrast, water mineralization seems to acquired by dissolution of minerals in the aquifer system especially halie and gypsum. Besides ion exchange processes play also an important role in the groundwater mineralization. Therefore, it clearly appears that several sources might contribute with different mineralization to the selenization of the aquifer through the natural recharge and also through the return of water irrigation. The contamination of the Mio-Pliocene shallow aquifer by a mixture with seawater is confirmed, and stable isotopes data do not support the hypothesis of mixing with seawater. (Author)

Characterising the vertical separation of shale-gas source rocks and aquifers across England and Wales (UK)

Science.gov (United States)

Loveless, Sian E.; Bloomfield, John P.; Ward, Robert S.; Hart, Alwyn J.; Davey, Ian R.; Lewis, Melinda A.

2018-03-01

Shale gas is considered by many to have the potential to provide the UK with greater energy security, economic growth and jobs. However, development of a shale gas industry is highly contentious due to environmental concerns including the risk of groundwater pollution. Evidence suggests that the vertical separation between exploited shale units and aquifers is an important factor in the risk to groundwater from shale gas exploitation. A methodology is presented to assess the vertical separation between different pairs of aquifers and shales that are present across England and Wales. The application of the method is then demonstrated for two of these pairs—the Cretaceous Chalk Group aquifer and the Upper Jurassic Kimmeridge Clay Formation, and the Triassic sandstone aquifer and the Carboniferous Bowland Shale Formation. Challenges in defining what might be considered criteria for `safe separation' between a shale gas formation and an overlying aquifer are discussed, in particular with respect to uncertainties in geological properties, aquifer extents and determination of socially acceptable risk levels. Modelled vertical separations suggest that the risk of aquifer contamination from shale exploration will vary greatly between shale-aquifer pairs and between regions and this will need to be considered carefully as part of the risk assessment and management for any shale gas development.

A multi-objective optimization framework for surfactant-enhanced remediation of DNAPL contaminations

NARCIS (Netherlands)

Schaerlaekens, J.; Mertens, J.; Van Linden, J.; Vermeiren, G.; Carmeliet, J.; Feyen, J.

2006-01-01

The occurrence of Dense Non-Aqueous Phase Liquid (DNAPL) contaminations in the subsurface is a threat for drinkwater resources in the western world. Surfactant-Enhanced Aquifer Remediation (SEAR) is widely considered as one of the most promising techniques to remediate DNAPL contaminations in-situ,

Pathways of sulfate and hydrogen sulfide transformations in a BTEX- contaminated groundwater system

DEFF Research Database (Denmark)

Einsiedl, Florian; Anneser, B.; Griebler, C.

2010-01-01

in complex environmental systems. As a result, compound specific stable isotope signatures in various sulfur species were determined in a tar-oil contaminated site and were linked to the microbial community distribution in the aquifer. The goal of the study was to reach an integrated understanding of sulfur...... intermediate during abiotic oxidation of hydrogen sulphide, with the latter formed during bacterial sulfate reduction. The formed elemental sulfur may be used by the specific microbial community found in this aquifer for the oxidation of organic contaminants such as toluene. In contrast, reoxidation...... of hydrogen sulfide to sulfate by molecular oxygen may affect sulfur cycling within the transition between the unsaturated and the saturated zones and therefore attenuate concentrations of contaminants in groundwater as well....

Arsenic mobilization in an alluvial aquifer of the Terai region, Nepal

Directory of Open Access Journals (Sweden)

Jasmine Diwakar

2015-09-01

New Hydrological Insights for the Region: The aquifer is characterized by Ca-HCO3 type water and is multi-contaminated, with the WHO guideline values exceeded for As, Mn and F in 80%, 70% and 40% of cases respectively. The middle portion of the floodplain was heavily contaminated with As, predominantly as As(III. The river water displayed some evidence of reductive processes in the hyporheic zone contributing As, Fe and Mn to baseflow and also had elevated fluoride. The generally sub-oxic conditions, dominance of As(III and Fe2+ species and positive correlation between As and both NH3 and UV-absorbance at 254 nm suggests that oxidation of organic matter coupled with microbial mediated reductive processes are important for mobilizing As in the aquifer. The apparent decoupling between As(III(aq and Fe2+(aq may be explained by precipitation of siderite, but further work is required to resolve this unambiguously. Along with reductive processes, other geochemical mechanisms including silicate weathering and precipitation/dissolution of carbonate minerals, control the solute and major ion composition of groundwater.

Influence of Solvent-Solvent and Solute-Solvent Interaction Properties on Solvent-Mediated Potential

International Nuclear Information System (INIS)

Zhou Shiqi

2005-01-01

A recently proposed universal calculational recipe for solvent-mediated potential is applied to calculate excess potential of mean force between two large Lennard-Jones (LJ) or hard core attractive Yukawa particles immersed in small LJ solvent bath at supercritical state. Comparison between the present prediction with a hypernetted chain approximation adopted for solute-solute correlation at infinitely dilute limit and existing simulation data shows high accuracy for the region with large separation, and qualitative reliability for the solute particle contact region. The calculational simplicity of the present recipe allows for a detailed investigation on the effect of the solute-solvent and solvent-solvent interaction details on the excess potential of mean force. The resultant conclusion is that gathering of solvent particles near a solute particle leads to repulsive excess PMF, while depletion of solvent particles away from the solute particle leads to attractive excess PMF, and minor change of the solvent-solvent interaction range has large influence on the excess PMF.

Conceptual understanding and groundwater quality of selected basin-fill aquifers in the Southwestern United States

Science.gov (United States)

Thiros, Susan A.; Bexfield, Laura M.; Anning, David W.; Huntington, Jena M.

2010-01-01

The National Water-Quality Assessment (NAWQA) Program of the U.S. Geological Survey has been conducting a regional analysis of water quality in the principal aquifer systems in the southwestern United States (hereinafter, “Southwest”) since 2005. Part of the NAWQA Program, the objective of the Southwest Principal Aquifers (SWPA) study is to develop a better understanding of water quality in basin-fill aquifers in the region by synthesizing information from case studies of 15 basins into a common set of important natural and human-related factors found to affect groundwater quality.The synthesis consists of three major components:1. Summary of current knowledge about the groundwater systems, and the status of, changes in, and influential factors affecting quality of groundwater in basin-fill aquifers in 15 basins previously studied by NAWQA (this report).2. Development of a conceptual model of the primary natural and human-related factors commonly affecting groundwater quality, thereby building a regional understanding of the susceptibility and vulnerability of basin-fill aquifers to contaminants.3. Development of statistical models that relate the concentration or occurrence of specific chemical constituents in groundwater to natural and human-related factors linked to the susceptibility and vulnerability of basin-fill aquifers to contamination.Basin-fill aquifers occur in about 200,000 mi2 of the 410,000 mi2 SWPA study area and are the primary source of groundwater supply for cities and agricultural communities. Four of the principal aquifers or aquifer systems of the United States are included in the basin-fill aquifers of the study area: (1) the Basin and Range basin-fill aquifers in California, Nevada, Utah, and Arizona; (2) the Rio Grande aquifer system in New Mexico and Colorado; (3) the California Coastal Basin aquifers; and (4) the Central Valley aquifer system in California. Because of the generally limited availability of surface-water supplies in

Nature and extent of lava-flow aquifers beneath Pahute Mesa, Nevada Test Site

Energy Technology Data Exchange (ETDEWEB)

Prothro, L.B.; Drellack, S.L. Jr.

1997-09-01

Work is currently underway within the Underground Test Area subproject of the US Department of Energy/Nevada Operations Office Environmental Restoration Program to develop corrective action plans in support of the overall corrective action strategy for the Nevada Test Site as established in the Federal Facility Agreement and Consent Order (FFACO, 1996). A closure plan is currently being developed for Pahute Mesa, which has been identified in the FFACO as consisting of the Western and Central Pahute Mesa Corrective Action Units. Part of this effort requires that hydrogeologic data be compiled for inclusion in a regional model that will be used to predict a contaminant boundary for these Corrective Action Units. Hydrogeologic maps have been prepared for use in the model to define the nature and extent of aquifers and confining units that might influence the flow of contaminated groundwater from underground nuclear tests conducted at Pahute Mesa. Much of the groundwater flow beneath Pahute Mesa occurs within lava-flow aquifers. An understanding of the distribution and hydraulic character of these important hydrogeologic units is necessary to accurately model groundwater flow beneath Pahute Mesa. This report summarizes the results of a study by Bechtel Nevada geologists to better define the hydrogeology of lava-flow aquifers at Pahute Mesa. The purpose of this study was twofold: (1) aid in the development of the hydrostratigraphic framework for Pahute Mesa, and (2) provide information on the distribution and hydraulic character of lava-flow aquifers beneath Pahute Mesa for more accurate computer modeling of the Western and Central Pahute Mesa Corrective Action Units.

Cone penetrometer testing (CPT) for groundwater contamination

International Nuclear Information System (INIS)

Jordan, J.E.; Van Pelt, R.S.

1993-01-01

Over the past decade, researchers at the Savannah River Site (SRS) and elsewhere have greatly advanced the knowledge of waste site characterization technologies. As a result, many of the techniques used in the past to investigate waste sites have been replaced by newer technologies, designed to provide greater protection for human health and the environment, greater access to suspected zones of contamination, and more accurate information of subsurface conditions. Determining the most environmentally sound method of assessing a waste unit is a major component of the SRS environmental restoration program. In an effort to understand the distribution and migration of contaminants in the groundwater system, the cone penetrometer investigation of the A/M-Area Southern Sector was implemented. The program incorporated a phased approach toward characterization by first using the CPT to delineate the plume boundary, followed by installing groundwater monitoring wells. The study provided the additional hydrogeologic information necessary to better understand the nature and extent of the contaminant plume (Fig. 1) and the hydrogeologic system in the Southem Sector. This data is essential for the optimal layout of the planned groundwater monitoring well network and recovery system to remediate the aquifers in the area. A number of other test locations were selected in the area during this study for lithologic calibration of the tool and to collect confirmation water samples from the aquifer. Cone penetrometer testing and hydrocone sampling, were performed at 17 sites (Fig. 2). The hydrocone, a tool modification to the CPT, was used to collect four groundwater samples from confined aquifers. These samples were analyzed by SRS laboratories. Elevated levels of chlorinated compounds were detected from these samples and have aided in further delineating the southern sector contaminant plume

Filtration and transport of Bacillus subtilis spores and the F-RNA phage MS2 in a coarse alluvial gravel aquifer: implications in the estimation of setback distances.

Science.gov (United States)

Pang, Liping; Close, Murray; Goltz, Mark; Noonan, Mike; Sinton, Lester

2005-04-01

Filtration of Bacillus subtilis spores and the F-RNA phage MS2 (MS2) on a field scale in a coarse alluvial gravel aquifer was evaluated from the authors' previously published data. An advection-dispersion model that is coupled with first-order attachment kinetics was used in this study to interpret microbial concentration vs. time breakthrough curves (BTC) at sampling wells. Based on attachment rates (katt) that were determined by applying the model to the breakthrough data, filter factors (f) were calculated and compared with f values estimated from the slopes of log (cmax/co) vs. distance plots. These two independent approaches resulted in nearly identical filter factors, suggesting that both approaches are useful in determining reductions in microbial concentrations over transport distance. Applying the graphic approach to analyse spatial data, we have also estimated the f values for different aquifers using information provided by some other published field studies. The results show that values of f, in units of log (cmax/co) m(-1), are consistently in the order of 10(-2) for clean coarse gravel aquifers, 10(-3) for contaminated coarse gravel aquifers, and generally 10(-1) for sandy fine gravel aquifers and river and coastal sand aquifers. For each aquifer category, the f values for bacteriophages and bacteria are in the same order-of-magnitude. The f values estimated in this study indicate that for every one-log reduction in microbial concentration in groundwater, it requires a few tens of meters of travel in clean coarse gravel aquifers, but a few hundreds of meters in contaminated coarse gravel aquifers. In contrast, a one-log reduction generally only requires a few meters of travel in sandy fine gravel aquifers and sand aquifers. Considering the highest concentration in human effluent is in the order of 10(4) pfu/l for enteroviruses and 10(6) cfu/100 ml for faecal coliform bacteria, a 7-log reduction in microbial concentration would comply with the drinking

The fate of benzotriazole pollutants in an urban oxic intergranular aquifer.

Science.gov (United States)

Trček, Branka; Žigon, Dušan; Zidar, Vlasta Kramarič; Auersperger, Primož

2017-12-26

Benzotriazoles (BTs) are considered as Contaminants of Emerging Concern (CECs); however, information about their fate in aquifers continues to be absent. This was the focus of the present study, which provides the first evidence for relevant BTs' degradation products (BTTPs) in urban aquifers that may impact the groundwater quality. The mechanisms and biotransformation pathways of BTs were investigated in an oxic intergranular medium. The BTs and BTTPs were identified and quantified by gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS) analytical techniques based on reference standards and internal materials. The major transformation products were identified as 2-methyl-2H-benzotriazole (2-MeBT) for the degradation of 1H-benzotriazole (BT) and as 2,4-dimethyl-2H-benzotriazole (2,4-dMeBT) and 1,4-dimethyl-1H-benzotriazole (1,4-dMeBT) for the degradation of 4-methyl-1H-benzotriazole (4-MeBT), and most probably also 5-methyl-1H-benzotriazole (5-MeBT). The leakage of wastewater pipelines is most probably the source of BTs. Sediments with a lower hydraulic conductivity give rise to perched aquifer conditions that lead to the temporal storage of leaking effluents and presumably the majority of BTs' transformation processes via methylation and tautomerization. The most stable BTTPs entered the saturated zone of the aquifer, where they prevailed. Concentrations up to 1500 ng L -1 were measured for the 2,4-dMeBT, which suggest a contamination risk for groundwater that is or may be used as a source for drinking water in the case of a constant input of pollutant loads from sewer systems. Copyright © 2017 Elsevier Ltd. All rights reserved.

A new risk and stochastic analysis of monitoring and remediation in subsurface contamination

Science.gov (United States)

Papapetridis, K.; Paleologos, E.

2012-04-01

Sanitary landfills constitute the most widely used management approach for the disposal of solid wastes because of their simplicity and cost effectiveness. However, historical records indicate that landfills exhibit a high failure rate of groundwater contamination. Successful detection of aquifer contamination via monitoring wells is a complicated problem with many factors, such as the heterogeneity of the geologic environment, the dispersion of contamination into the geologic medium, the quantity and nature of the contaminants, the number and location of the monitoring wells, and the frequency of sampling, all contributing to the uncertainty of early detection. Detection of contaminants, of course, is of value if remedial actions follow as soon as possible, so that the volume of contaminated groundwater to be treated is minimized. Practically, there is always a time lag between contaminant detection and remedial action response. Administrative decisions and arrangements with local contractors initiate remedial procedures introduces a time lag between detection and remediation time. During this time lag a plume continues to move into an aquifer contaminating larger groundwater volumes. In the present study these issues are addressed by investigating the case of instantaneous leakage from a landfill facility into a heterogeneous aquifer. The stochastic Monte Carlo framework was used to address, in two dimensions, the problem of evaluating the effectiveness of contaminant detection in heterogeneous aquifers by linear networks of monitoring wells. Numerical experiments based on the random-walk tracking-particle method were conducted to determine the detection probabilities and to calculate contaminated areas at different time steps. Several cases were studied assuming different levels of geologic heterogeneity, contamination dispersion, detectable contamination limits and monitoring wells' sampling frequencies. A new perspective is introduced for the correction of

Correlation between nitrate concentration in groundwater and parameters affecting aquifer intrinsic vulnerability

Science.gov (United States)

Debernardi, Laura; de Luca, Domenico Antonio; Lasagna, Manuela

2008-08-01

This paper is the result of a study which was carried out in order to verify if the traditional methods to evaluate the intrinsic vulnerability or vulnerability related parameters, are able to clarify the problem of nitrate pollution in groundwater. In particular, the aim was to evaluate limitations and problems connected to aquifer vulnerability methods applied to nitrate contamination prevision in groundwater. The investigation was carried out by comparing NO3 - concentrations, measured in March and November 2004 in the shallow aquifer, and the vulnerability classes, obtained by using GOD and TOT methods. Moreover, it deals with a comparison between NO3 - concentrations and single parameters (depth to water table, land use and nitrogen input). The study area is the plain sector of Piemonte (Northern Italy), where an unconfined aquifer nitrate contamination exists. In this area the anthropogenic presence is remarkable and the input of N-fertilizers and zootechnical effluents to the soil cause a growing amount of nitrates in groundwater. This approach, used in a large area (about 10,000 km2) and in several monitoring wells (about 500), allowed to compare the efficiency of different vulnerability methods and to verify the importance of every parameter on the nitrate concentrations in the aquifer. Furthermore it allowed to obtain interesting correlations in different hydrogeological situations. Correlations between depth to water table, land use and nitrogen input to the soil with nitrate concentrations in groundwater show unclear situations: in fact these comparisons describe the phenomenon trend and highlight the maximum nitrate concentrations for each circumstance but often show wide ranges of possible nitrate concentrations. The same situation could be observed by comparing vulnerability indexes and nitrate concentrations in groundwater. These results suggest that neither single parameters nor vulnerability methods (GOD and TOT) are able to describe individually

Aquifer sensitivity to pesticide leaching: Testing a soils and hydrogeologic index method

Science.gov (United States)

Mehnert, E.; Keefer, D.A.; Dey, W.S.; Wehrmann, H.A.; Wilson, S.D.; Ray, C.

2005-01-01

For years, researchers have sought index and other methods to predict aquifer sensitivity and vulnerability to nonpoint pesticide contamination. In 1995, an index method and map were developed to define aquifer sensitivity to pesticide leaching based on a combination of soil and hydrogeologic factors. The soil factor incorporated three soil properties: hydraulic conductivity, amount of organic matter within individual soil layers, and drainage class. These properties were obtained from a digital soil association map. The hydrogeologic factor was depth to uppermost aquifer material. To test this index method, a shallow ground water monitoring well network was designed, installed, and sampled in Illinois. The monitoring wells had a median depth of 7.6 m and were located adjacent to corn and soybean fields where the only known sources of pesticides were those used in normal agricultural production. From September 1998 through February 2001, 159 monitoring wells were sampled for 14 pesticides but no pesticide metabolites. Samples were collected and analyzed to assess the distribution of pesticide occurrence across three units of aquifer sensitivity. Pesticides were detected in 18% of all samples and nearly uniformly from samples from the three units of aquifer sensitivity. The new index method did not predict pesticide occurrence because occurrence was not dependent on the combined soil and hydrogeologic factors. However, pesticide occurrence was dependent on the tested hydrogeologic factor and was three times higher in areas where the depth to the uppermost aquifer was <6 m than in areas where the depth to the uppermost aquifer was 6 to <15 m. Copyright ?? 2005 National Ground Water Association.

Model-based assessment of the potential of seasonal aquifer thermal energy storage and recovery as a groundwater ecosystem service for the Brussels-Capital Region

Science.gov (United States)

Anibas, Christian; Huysmans, Marijke

2015-04-01

transport models on several pilot sites within this region, our study aims to better quantify the potential for ATES systems in these aquifers. Covering several dozen square kilometres, the models investigate interaction processes between ATES installations and other competing groundwater usages, including groundwater abstraction. Based on the model results ecological and economical balance calculations should better define the effects of ATES systems. Aimed at experts and decision makers this research project delivers a detailed foundation for the exploitation of seasonal aquifer thermal storage in the aquifers of the Brussels-Capital Region as an ecosystem service, and should assist in establishing guidelines for planning, building and maintaining high performing ATES systems. References BONTE, M., STUYFZAND, P.J., HULSMANN, A., VAN BEELEN, P. (2011): Underground thermal energy storage: environmental risks and policy developments in the Netherlands and European Union. Ecology and Society 16 (1): 22. VITO, (2007): Studie van de geothermische en hydrothermische technieken die toepasbaar zijn in Brussel: wettelijke context, milieu-impact, goede praktijk en economisch potentieel (in Dutch); Mol, Belgium. ZUURBIER, K.G., HARTOG, N., VALSTAR, J., POST, V.E., VAN BREUKELEN, B.M., (2013): The impact of low temperature seasonal aquifer thermal energy storage (SATES) systems on chlorinated solvent contaminated groundwater: modeling of spreading and degradation. Journal of Contaminant Hydrology 147: 1-13.

Develop Documentation/Prepare Remedial Action Concept Plan for Building 24 Contamination Plume at Picatinny Arsenal

National Research Council Canada - National Science Library

1989-01-01

.... TCE and other solvents were used in degreasing operations at this metal shop. Three dimensional models of ground water flow and solute transport were developed and applied to the TCE plume in the shallow aquifers around building 24...

Estimating preferential flow in karstic aquifers using statistical mixed models.

Science.gov (United States)

Anaya, Angel A; Padilla, Ingrid; Macchiavelli, Raul; Vesper, Dorothy J; Meeker, John D; Alshawabkeh, Akram N

2014-01-01

Karst aquifers are highly productive groundwater systems often associated with conduit flow. These systems can be highly vulnerable to contamination, resulting in a high potential for contaminant exposure to humans and ecosystems. This work develops statistical models to spatially characterize flow and transport patterns in karstified limestone and determines the effect of aquifer flow rates on these patterns. A laboratory-scale Geo-HydroBed model is used to simulate flow and transport processes in a karstic limestone unit. The model consists of stainless steel tanks containing a karstified limestone block collected from a karst aquifer formation in northern Puerto Rico. Experimental work involves making a series of flow and tracer injections, while monitoring hydraulic and tracer response spatially and temporally. Statistical mixed models (SMMs) are applied to hydraulic data to determine likely pathways of preferential flow in the limestone units. The models indicate a highly heterogeneous system with dominant, flow-dependent preferential flow regions. Results indicate that regions of preferential flow tend to expand at higher groundwater flow rates, suggesting a greater volume of the system being flushed by flowing water at higher rates. Spatial and temporal distribution of tracer concentrations indicates the presence of conduit-like and diffuse flow transport in the system, supporting the notion of both combined transport mechanisms in the limestone unit. The temporal response of tracer concentrations at different locations in the model coincide with, and confirms the preferential flow distribution generated with the SMMs used in the study. © 2013, National Ground Water Association.

20 years of long-term atrazine monitoring in a shallow aquifer in western Germany.

Science.gov (United States)

Vonberg, David; Vanderborght, Jan; Cremer, Nils; Pütz, Thomas; Herbst, Michael; Vereecken, Harry

2014-03-01

Atrazine was banned in Germany in 1991 due to findings of atrazine concentrations in ground- and drinking waters exceeding threshold values. Monitoring of atrazine concentrations in the groundwater since then provides information about the resilience of the groundwater quality to changing agricultural practices. In this study, we present results of a monitoring campaign of atrazine concentrations in the Zwischenscholle aquifer. This phreatic aquifer is exposed to intensive agricultural land use and susceptible to contaminants due to a shallow water table. In total 60 observation wells (OWs) have been monitored since 1991, of which 15 are sampled monthly today. Descriptive statistics of monitoring data were derived using the "regression on order statistics" (ROS) data censoring approach, estimating values for nondetects. The monitoring data shows that even 20 years after the ban of atrazine, the groundwater concentrations of sampled OWs remain on a level close to the threshold value of 0.1 μg l(-1) without any considerable decrease. The spatial distribution of atrazine concentrations is highly heterogeneous with OWs exhibiting permanently concentrations above the regulatory threshold on the one hand and OWs were concentrations are mostly below the limit of quantification (LOQ) on the other hand. A deethylatrazine-to-atrazine ratio (DAR) was used to distinguish between diffuse - and point-source contamination, with a global mean value of 0.84 indicating mainly diffuse contamination. Principle Component Analysis (PCA) of the monitoring dataset demonstrated relationships between the metabolite desisopropylatrazine, which was found to be exclusively associated with the parent compound simazine but not with atrazine, and between deethylatrazine, atrazine, nitrate, and the specific electrical conductivity. These parameters indicate agricultural impacts on groundwater quality. The findings presented in this study point at the difficulty to estimate mean concentrations

Low-rank Kalman filtering for efficient state estimation of subsurface advective contaminant transport models

KAUST Repository

El Gharamti, Mohamad; Hoteit, Ibrahim; Sun, Shuyu

2012-01-01

Accurate knowledge of the movement of contaminants in porous media is essential to track their trajectory and later extract them from the aquifer. A two-dimensional flow model is implemented and then applied on a linear contaminant transport model

Controlling geological and hydrogeological processes in an arsenic contaminated aquifer on the Red River flood plain, Vietnam

International Nuclear Information System (INIS)

Larsen, Flemming; Nhan Quy Pham; Nhan Duc Dang; Postma, Dieke; Jessen, Soren; Viet Hung Pham; Nguyen, Thao Bach; Trieu, Huy Duc; Luu Thi Tran; Hoan Nguyen; Chambon, Julie; Hoan Van Nguyen; Dang Hoang Ha; Nguyen Thi Hue; Mai Thanh Duc; Refsgaard, Jens Christian

2008-01-01

Geological and hydrogeological processes controlling recharge and the mobilization of As were investigated in a shallow Holocene aquifer on the Red River flood plain near Hanoi, Vietnam. The geology was investigated using surface resistivity methods, geophysical borehole logging, drilling of boreholes and installation of more than 200 piezometers. Recharge processes and surface-groundwater interaction were studied using (i) time-series of hydraulic head distribution in surface water and aquifers, (ii) the stable isotope composition of waters and (iii) numerical groundwater modeling. The Red River and two of its distributaries run through the field site and control the groundwater flow pattern. For most of the year, there is a regional groundwater flow towards the Red River. During the monsoon the Red River water stage rises up to 6 m and stalls the regional groundwater flow. The two distributaries recharge the aquifer from perched water tables in the dry season, whilst in the flooding period surface water enters the aquifer through highly permeable bank sediments. The result is a dynamic groundwater flow pattern with rapid fluctuations in the groundwater table. A transient numerical model of the groundwater flow yields an average recharge rate of 60-100 mm/a through the confining clay, and a total recharge of approximately 200 mm/a was estimated from 3 H/ 3 He dating of the shallow groundwater. Thus in the model area, recharge of surface water from the river distributaries and recharge through a confining clay is of the same magnitude, being on average around 100 mm/a. The thickness of the confining clay varies between 2 and 10 m, and affects the recharge rate and the transport of electron acceptors (O 2 , NO 3 - and SO 4 2- ) into the aquifer. Where the clay layer is thin, an up to 2 m thick oxic zone develops in the shallow aquifer. In the oxic zone the As concentration is less than 1 μg/L but increases in the reduced zone below to 550 μg/L. In the Holocene

Evaluation of mercury and physicochemical parameters in different depths of aquifer water of Thar coalfield, Pakistan.

Science.gov (United States)

Ali, Jamshed; Kazi, Tasneem G; Tuzen, Mustafa; Ullah, Naeem

2017-07-01

In the current study, mercury (Hg) and physicochemical parameters have been evaluated in aquifer water at different depths of Thar coal field. The water samples were collected from first aquifer (AQ 1 ), second aquifer (AQ 2 ), and third aquifer (AQ 3 ) at three depths, 50-60, 100-120, and 200-250 m, respectively. The results of aquifer water of three depths were interpreted by using different multivariate statistical techniques. Validation of desired method was checked by spiking standard addition method in studied aquifer water samples. The content of Hg in aquifer water samples was measured by cold vapor atomic absorption spectrometer (CV-AAS). These determined values illustrate that the levels of Hg were higher than WHO recommended values for drinking water. All physicochemical parameters were higher than WHO permissible limits for drinking water except pH and SO 4 2- in aquifer water. The positive correlation of Hg with other metals in aquifer water samples of AQ 1 , AQ 2 , and AQ 3 of Thar coalfield except HCO 3 - was observed which might be caused by geochemical minerals. The interpretation of determined values by the cluster technique point out the variations within the water quality parameter as well as sampling location of studied field. The aquifer water AQ 2 was more contaminated with Hg as compared to AQ 1 and AQ 3 ; it may be due to leaching of Hg from coal zone. The concentration of Hg in aquifer water obtained from different depths was found in the following decreasing order: AQ 2  < AQ 1  < AQ 3 .

Fate of Arsenic during Red River Water Infiltration into Aquifers beneath Hanoi, Vietnam.

Science.gov (United States)

Postma, Dieke; Mai, Nguyen Thi Hoa; Lan, Vi Mai; Trang, Pham Thi Kim; Sø, Helle Ugilt; Nhan, Pham Quy; Larsen, Flemming; Viet, Pham Hung; Jakobsen, Rasmus

2017-01-17

Recharge of Red River water into arsenic-contaminated aquifers below Hanoi was investigated. The groundwater age at 40 m depth in the aquifer underlying the river was 1.3 ± 0.8 years, determined by tritium-helium dating. This corresponds to a vertical flow rate into the aquifer of 19 m/year. Electrical conductivity and partial pressure of CO 2 (P CO 2 ) indicate that water recharged from the river is present in both the sandy Holocene and gravelly Pleistocene aquifers and is also abstracted by the pumping station. Infiltrating river water becomes anoxic in the uppermost aquifer due to the oxidation of dissolved organic carbon. Further downward, sedimentary carbon oxidation causes the reduction of As-containing Fe-oxides. Because the release of arsenic by reduction of Fe-oxides is controlled by the reaction rate, arsenic entering the solution becomes highly diluted in the high water flux and contributes little to the groundwater arsenic concentration. Instead, the As concentration in the groundwater of up to 1 μM is due to equilibrium-controlled desorption of arsenic, adsorbed to the sediment before river water started to infiltrate due to municipal pumping. Calculations indicate that it will take several decades of river water infiltration to leach arsenic from the Holocene aquifer to below the World Health Organization limit of 10 μg/L.

Fate of Arsenic during Red River Water Infiltration into Aquifers beneath Hanoi, Vietnam

Science.gov (United States)

2016-01-01

Recharge of Red River water into arsenic-contaminated aquifers below Hanoi was investigated. The groundwater age at 40 m depth in the aquifer underlying the river was 1.3 ± 0.8 years, determined by tritium–helium dating. This corresponds to a vertical flow rate into the aquifer of 19 m/year. Electrical conductivity and partial pressure of CO2 (PCO2) indicate that water recharged from the river is present in both the sandy Holocene and gravelly Pleistocene aquifers and is also abstracted by the pumping station. Infiltrating river water becomes anoxic in the uppermost aquifer due to the oxidation of dissolved organic carbon. Further downward, sedimentary carbon oxidation causes the reduction of As-containing Fe-oxides. Because the release of arsenic by reduction of Fe-oxides is controlled by the reaction rate, arsenic entering the solution becomes highly diluted in the high water flux and contributes little to the groundwater arsenic concentration. Instead, the As concentration in the groundwater of up to 1 μM is due to equilibrium-controlled desorption of arsenic, adsorbed to the sediment before river water started to infiltrate due to municipal pumping. Calculations indicate that it will take several decades of river water infiltration to leach arsenic from the Holocene aquifer to below the World Health Organization limit of 10 μg/L. PMID:27958705

Restoration of Wadi Aquifers by Artificial Recharge with Treated Waste Water

KAUST Repository

Missimer, Thomas M.

2012-04-26

Fresh water resources within the Kingdom of Saudi Arabia are a rare and precious commodity that must be managed within a context of integrated water management. Wadi aquifers contain a high percentage of the naturally occurring fresh groundwater in the Kingdom. This resource is currently overused and has become depleted or contaminated at many locations. One resource that could be used to restore or enhance the fresh water resources within wadi aquifers is treated municipal waste water (reclaimed water). Each year about 80 percent of the country\\'s treated municipal waste water is discharged to waste without any beneficial use. These discharges not only represent a lost water resource, but also create a number of adverse environmental impacts, such as damage to sensitive nearshore marine environments and creation of high-salinity interior surface water areas. An investigation of the hydrogeology of wadi aquifers in Saudi Arabia revealed that these aquifers can be used to develop aquifer recharge and recovery (ARR) systems that will be able to treat the impaired-quality water, store it until needed, and allow recovery of the water for transmittal to areas in demand. Full-engineered ARR systems can be designed at high capacities within wadi aquifer systems that can operate in concert with the natural role of wadis, while providing the required functions of additional treatment, storage and recovery of reclaimed water, while reducing the need to develop additional, energy-intensive desalination to meet new water supply demands. © 2012, The Author(s). Ground Water © 2012, National Ground Water Association.

Restoration of wadi aquifers by artificial recharge with treated waste water.

Science.gov (United States)

Missimer, Thomas M; Drewes, Jörg E; Amy, Gary; Maliva, Robert G; Keller, Stephanie

2012-01-01

Fresh water resources within the Kingdom of Saudi Arabia are a rare and precious commodity that must be managed within a context of integrated water management. Wadi aquifers contain a high percentage of the naturally occurring fresh groundwater in the Kingdom. This resource is currently overused and has become depleted or contaminated at many locations. One resource that could be used to restore or enhance the fresh water resources within wadi aquifers is treated municipal waste water (reclaimed water). Each year about 80 percent of the country's treated municipal waste water is discharged to waste without any beneficial use. These discharges not only represent a lost water resource, but also create a number of adverse environmental impacts, such as damage to sensitive nearshore marine environments and creation of high-salinity interior surface water areas. An investigation of the hydrogeology of wadi aquifers in Saudi Arabia revealed that these aquifers can be used to develop aquifer recharge and recovery (ARR) systems that will be able to treat the impaired-quality water, store it until needed, and allow recovery of the water for transmittal to areas in demand. Full-engineered ARR systems can be designed at high capacities within wadi aquifer systems that can operate in concert with the natural role of wadis, while providing the required functions of additional treatment, storage and recovery of reclaimed water, while reducing the need to develop additional, energy-intensive desalination to meet new water supply demands. © 2012, The Author(s). Ground Water © 2012, National Ground Water Association.

Use of computer programs STLK1 and STWT1 for analysis of stream-aquifer hydraulic interaction

Science.gov (United States)

Desimone, Leslie A.; Barlow, Paul M.

1999-01-01

Quantifying the hydraulic interaction of aquifers and streams is important in the analysis of stream base fow, flood-wave effects, and contaminant transport between surface- and ground-water systems. This report describes the use of two computer programs, STLK1 and STWT1, to analyze the hydraulic interaction of streams with confined, leaky, and water-table aquifers during periods of stream-stage fuctuations and uniform, areal recharge. The computer programs are based on analytical solutions to the ground-water-flow equation in stream-aquifer settings and calculate ground-water levels, seepage rates across the stream-aquifer boundary, and bank storage that result from arbitrarily varying stream stage or recharge. Analysis of idealized, hypothetical stream-aquifer systems is used to show how aquifer type, aquifer boundaries, and aquifer and streambank hydraulic properties affect aquifer response to stresses. Published data from alluvial and stratifed-drift aquifers in Kentucky, Massachusetts, and Iowa are used to demonstrate application of the programs to field settings. Analytical models of these three stream-aquifer systems are developed on the basis of available hydrogeologic information. Stream-stage fluctuations and recharge are applied to the systems as hydraulic stresses. The models are calibrated by matching ground-water levels calculated with computer program STLK1 or STWT1 to measured ground-water levels. The analytical models are used to estimate hydraulic properties of the aquifer, aquitard, and streambank; to evaluate hydrologic conditions in the aquifer; and to estimate seepage rates and bank-storage volumes resulting from flood waves and recharge. Analysis of field examples demonstrates the accuracy and limitations of the analytical solutions and programs when applied to actual ground-water systems and the potential uses of the analytical methods as alternatives to numerical modeling for quantifying stream-aquifer interactions.

Ground-water quality in the carbonate-rock aquifer of the Great Basin, Nevada and Utah, 2003

Science.gov (United States)

Schaefer, Donald H.; Thiros, Susan A.; Rosen, Michael R.

2005-01-01

The carbonate-rock aquifer of the Great Basin is named for the thick sequence of Paleozoic limestone and dolomite with lesser amounts of shale, sandstone, and quartzite. It lies primarily in the eastern half of the Great Basin and includes areas of eastern Nevada and western Utah as well as the Death Valley area of California and small parts of Arizona and Idaho. The carbonate-rock aquifer is contained within the Basin and Range Principal Aquifer, one of 16 principal aquifers selected for study by the U.S. Geological Survey’s National Water- Quality Assessment Program.Water samples from 30 ground-water sites (20 in Nevada and 10 in Utah) were collected in the summer of 2003 and analyzed for major anions and cations, nutrients, trace elements, dissolved organic carbon, volatile organic compounds (VOCs), pesticides, radon, and microbiology. Water samples from selected sites also were analyzed for the isotopes oxygen-18, deuterium, and tritium to determine recharge sources and the occurrence of water recharged since the early 1950s.Primary drinking-water standards were exceeded for several inorganic constituents in 30 water samples from the carbonate-rock aquifer. The maximum contaminant level was exceeded for concentrations of dissolved antimony (6 μg/L) in one sample, arsenic (10 μg/L) in eleven samples, and thallium (2 μg/L) in one sample. Secondary drinking-water regulations were exceeded for several inorganic constituents in water samples: chloride (250 mg/L) in five samples, fluoride (2 mg/L) in two samples, iron (0.3 mg/L) in four samples, manganese (0.05 mg/L) in one sample, sulfate (250 mg/L) in three samples, and total dissolved solids (500 mg/L) in seven samples.Six different pesticides or metabolites were detected at very low concentrations in the 30 water samples. The lack of VOC detections in water sampled from most of the sites is evidence thatVOCs are not common in the carbonate-rock aquifer. Arsenic values for water range from 0.7 to 45.7 �

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

Science.gov (United States)

Brayton, Michael J.; Cruz, Roberto M.; Myers, Luke; Degnan, James R.; Raffensperger, Jeff P.

2015-01-01

From 1966 to 2002, activities at the Standard Chlorine of Delaware chemical facility in New Castle County, Delaware resulted in the contamination of groundwater, soils, and wetland sediment. In 2005, the U.S. Geological Survey (USGS), in partnership with the U.S. Environmental Protection Agency, Region 3, and the Delaware Department of Natural Resources and Environmental Control began a multi-year investigation of the hydrogeologic framework and hydrology of the confined aquifer system. The goals of the ongoing study at the site (the Potomac Aquifer Study) are to determine the hydraulic connection between the Columbia and Potomac aquifers, determine the direction of groundwater flow in the Potomac aquifer, and identify factors affecting the fate of contaminated groundwater. This report describes progress made towards these goals based on available data collected through September 2012.

Reactive dispersive contaminant transport in coastal aquifers: Numerical simulation of a reactive Henry problem

KAUST Repository

Nick, H.M.; Raoof, A.; Centler, F.; Thullner, M.; Regnier, P.

2013-01-01

The reactive mixing between seawater and terrestrial water in coastal aquifers influences the water quality of submarine groundwater discharge. While these waters come into contact at the seawater groundwater interface by density driven flow

Quality of water in alluvial aquifers in eastern Iowa

Science.gov (United States)

Savoca, Mark E.; Sadorf, Eric M.; Linhart, S. Michael; Barnes, Kimberlee K.

2001-01-01

The goal of the U.S. Geological Survey (USGS) National Water-Quality Assessment (NAWQA) Program is to assess the status and trends in the quality of the Nation's surface and ground water, and to better understand the natural and human factors affecting water quality. The Eastern Iowa Basins study unit encompasses an area of about 50,500 square kilometers (19,500 square miles) in eastern Iowa and southern Minnesota and is one of 59 study units in the NAWQA program. Land-use studies are an important component of the NAWQA program, and are designed to assess the concentration and distribution of water-quality constituents in recently recharged ground water associated with the most significant land use and hydrogeologic settings within a study unit. The focus of the land-use study in the Eastern Iowa Basins study unit is agricultural and urban land uses and alluvial aquifers. Agriculture is the dominant land use in the study unit. Urban areas, although not extensive, represent important potential source areas of contaminants associated with residential, commercial, and industrial activities. Alluvial aquifers are present throughout much of the study unit, and constitute a major ground-water supply that is susceptible to contamination from land-use activities.

Vulnerability assessment of the Toluca Valley aquifer combining a parametric approach and advective transport

International Nuclear Information System (INIS)

Gárfias, J.; Llanos, H.; Franco, R.; Martel, R.

2017-01-01

Groundwater vulnerability assessment is an important task in water resources and land management. Depending on the availability of data and the complexity of the hydrogeological conditions, different approaches can be adopted. As an alternative, this study involves the use of a combined approach based on vulnerability methods and advective particle tracking to better understand the susceptibility to contamination in the Toluca valley aquifer. An intrinsic vulnerability map (DRASTIC) was used to identify areas that are more susceptible to ground water contamination. To estimate advective particle tracking, we developed a 3D flow model using VisualModflow and MODPATH to describe the regional flow of groundwater. The vulnerability map demonstrates the problematic application and interpretation of qualitative the vulnerability method of the parametric system group, which indicates a difference of approximately 23% when compared with the modified vulnerability map. Potential contamination sources based on landfill sites were comparatively high; approximately 76% are located in areas that could be susceptible to contamination through vertical infiltration, especially those that are located along the Lerma system of wells. Industrial parks located in the centre of the valley (83%), where continuous extraction of groundwater and land subsidence occurs, have been classified as high vulnerability zones, increasing the risk of contaminants from surface sources reaching the groundwater. In order to understand the susceptibility to contamination in the aquifer, various delineation approaches should be adopted and all the results that validate each other should be considered, thus making a good strategy for implementing different degrees of protection measures. [es

Delineation of brine contamination in and near the East Poplar oil field, Fort Peck Indian Reservation, northeastern Montana, 2004-09

Science.gov (United States)

Thamke, Joanna N.; Smith, Bruce D.

2014-01-01

The extent of brine contamination in the shallow aquifers in and near the East Poplar oil field is as much as 17.9 square miles and appears to be present throughout the entire saturated zone in contaminated areas. The brine contamination affects 15–37 billion gallons of groundwater. Brine contamination in the shallow aquifers east of the Poplar River generally moves to the southwest toward the river and then southward in the Poplar River valley. The likely source of brine contamination in the shallow aquifers is brine that is produced with crude oil in the East Poplar oil field study area. Brine contamination has not only affected the water quality from privately owned wells in and near the East Poplar oil field, but also the city of Poplar’s public water-supply wells. Three water-quality types characterize water in the shallow aquifers; a fourth water-quality type in the study area characterizes the brine. Type 1 is uncontaminated water that is suitable for most domestic purposes and typically contains sodium bicarbonate and sodium/magnesium sulfate as the dominant ions. Type 2 is moderately contaminated water that is suitable for some domestic purposes, but not used for drinking water, and typically contains sodium and chloride as the dominant ions. Type 3 is considerably contaminated water that is unsuitable for any domestic purpose and always contains sodium and chloride as the dominant ions. Type 3 quality of water in the shallow aquifers is similar to Type 4, which is the brine that is produced with crude oil. Electromagnetic apparent conductivity data were collected in the 106 square-mile area and used to determine extent of brine contamination. These data were collected and interpreted in conjunction with water-quality data collected through 2009 to delineate brine plumes in the shallow aquifers. Monitoring wells subsequently were drilled in some areas without existing water wells to confirm most of the delineated brine plumes; however, several possible

Assessing Contamination Potential of Nitrate-N in Groundwater of Lanyang Plain

Science.gov (United States)

Liang, Ching-Ping; Tu, Yu-Lin; Lin, Chien-Wen; Jang, Cheng-Shin