A simple and convenient empirical survey method with a soil electrical conductivity meter for incineration residue-derived soil contamination

To facilitate field surveys for identifying areas of incineration residue-derived soil contamination, a simple and convenient method with a soil electrical conductivity meter was examined. First, the leaching test specified by Notification No. 13 of the Ministry of the Environment, 1973, was conducted on 506 samples of 11 types of wastes and compost, and the relationship between the concentrations of toxic elements [total Hg (T-Hg), Cd, Pb, Cr⁶⁺, and As] and values of electrical conductivity (EC) was examined. The results showed that bottom ash and fly ash were wastes with high EC values and that these wastes indicated higher levels of toxic elements. Second, an estimation method for the soil EC value of contaminated soil (ECc) was proposed based on the EC values of noncontaminated soil, and its usefulness was examined. The results of field surveys conducted at sites whose soils were suspected of contamination by dioxins and other pollutants derived from incineration residues showed that the contaminated spots and areas were identified by using ECc values. Moreover, comparison of the elemental contents of soils in terms of Cr, Ni, Zn, Na, K, Ca, Fe, Mn, and others, in addition to the above-mentioned toxic elements (excluding Cr⁶⁺), with those of the potential sources of pollution was verified to be effective for identifying the source of soil contamination.     

Petroleum Hydrocarbons Rhizodegradation by Sebastiania commersoniana (Baill.) L. B. SM. & Downs

Petroliferous activities in Brazil have an accelerated development in the last years. As a consequence, the incidence of environmental accidents such as oil spills and contamination of soils has increased significantly. Therefore, it is extremely necessary to develop remediation techniques with lower costs, decontamination efficiency and impact minimisation. The aim of this work was to evaluate Sebastiania commersoniana phytoremediation potential in soil contaminated by petroleum. This species, which is a native tree, was selected due to its proven capacity for surviving in areas contaminated by petroleum. Experiments were carried out with soils that were vegetated but non-contaminated, soils that were freshly contaminated (25, 50 and 75 g kg^?1) but non-vegetated, and soils that were vegetated and contaminated, samples were collected 60 and 424 days after contamination with the purpose of evaluating the percentage of petroleum degradation in relation to the time. The results obtained in the present study allow us to state that S. commersoniana proves to be tolerant to petroleum contamination with respect to plant’s growth. The degradation of petroleum hydrocarbons was evaluated by gas chromatography with a flame ionisation detector (GC-FID) equipped with a capillary column HP-5 (5% phenyl-methylpolysiloxane, 30 m; 0.25 mm; 0.25 μm). According to chromatographic analysis, samples in contact with S. commersoniana showed a significant area reduction of the hydrocarbon peaks. Analysis of the 60-day samples showed a reduction of petroleum hydrocarbons area higher than 60% and the 424-day samples showed a reduction higher than 94%, which demonstrates that a petroleum degradation process is occurring.     

Scenario‐Based Evaluation of Commercially Available Cleaning Robots for Collection of Bacillus Spores from Environmental Surfaces

The cleaning robots, a vacuum‐based robot (R2) and a wetted‐wipe‐based robot (R4), were evaluated in this study to determine their effectiveness for sampling Bacillus atrophaeus spores. The tests were designed to evaluate the benefit of robot sampling on large areas with two different contamination scenarios: a high‐concentration, low spatial extent contamination (hot spot) and a low concentration, high spatial extent contamination (widely dispersed). The hot spot tests were conducted with the high spore contamination (approximately 10⁷ colony forming units [CFUs]) on a limited area (30.5 cm × 30.5 cm), 2 percent of the entire test. The widely dispersed tests were conducted with approximately 0.1 CFUs/cm² for floor laminate and approximately 10 CFUs/cm² for carpet surfaces. The widely dispersed tests distributed spores across the test surface and covered approximately 40 percent of the entire test area. The test results showed that both robots successfully sampled a large quantity of spores from carpet and floor laminate surfaces for both test scenarios. Robot performance is discussed in the context of currently used surface sampling methods. © 2014 Wiley Periodicals, Inc.*     

Health risk assessment of heavy metals (Cr, Ni, Cu, Zn, Cd, Pb) in circumjacent soil of a factory for recycling waste electrical and electronic equipment

The aim of the study was to determine the potential environmental contamination in a typical factory for recycling waste electrical and electronic equipment in Shanghai. Heavy metals (Cr, Ni, Cu, Zn, Cd, Pb) in the soil around the factory have been evaluated in this paper. Compared with the background value, the concentrations of six metals detected in all the samples were higher, which showed that toxic metals were released into soil around the factory. Compared with the Environmental Quality Standards for Soils, China grade III, all the six metals are under soil guidelines. The non-cancer risk in different directions from the factory was in the order of: the north > the west > the south > the east. For inhalation and ingestion, the non-cancer risk in the soil west of the factory was biggest. Nevertheless, the non-cancer risk in the soil north of the factory was the biggest for dermal contact. The trend of cancer risk was the west > the south > the north > the east. The non-cancer risk and the carcinogenic risk for Cr, Ni, and Cd were all below the limiting value. This study might provide a reference for the risk assessment involved in electronic waste management and recycling activities.     

Chlorinated Hydrocarbon–Contaminated Site Investigation With Optimized 3D‐CSIA Approach

An optimized “Three‐Dimensional Compound Specific Isotope Analysis (3D‐CSIA)'' investigation was conducted at a chlorinated hydrocarbon–contaminated site in order to (1) determine if multiple onsite sources of groundwater contamination existed and (2) demonstrate the cost‐effectiveness of applying isotope fingerprinting at such a complex contaminated site. Previous groundwater investigations identified chlorinated hydrocarbons at levels that significantly exceed drinking‐water standards but failed to determine the source(s) of contamination due to the lack of vadose‐zone contamination and the absence of groundwater contaminants in shallow portions of the surficial aquifer. To better understand the contaminant source(s), groundwater samples were taken and tested for both the presence of chlorinated hydrocarbons and their isotopic signatures of ¹³C/¹²C, ³⁷Cl/³⁵Cl, and ²H/¹H. A site investigation with an optimized 3D‐CSIA approach revealed multiple chlorinated hydrocarbon releases from different sources, which was also cost‐effective considering the new lines of evidence of target contaminants obtained with the 3D‐CSIA approach instead of any traditional fingerprinting approaches. In addition, the 3D‐CSIA results inferred in situ bioremediation of chlorinated hydrocarbons would be feasible at the site. © 2013 Wiley Periodicals, Inc.     

Systematically selecting an alternative to remediate soil contaminating groundwater

Contaminated soil is a continuing source of ground water contamination at some hazardous waste sites. Even if that soil does not pose a threat to human health or the environment, soil remediation may benefit ground-water cleanup in terms of time, money, or protectiveness. A method has been developed to provide a systematic manner to select a soil cleanup alternative. Using commercially available Windows-based software, the method consists of the development of a decision tree whose chance nodes are the restoration time frame probability distributions. Uncertainty associated with site data is quantitatively evaluated using Monte Carlo analysis to develop the probability distributions. The decision tree selects the alternative with the lowest cost. Data from an actual remedial investigation/feasibility study demonstrate the ease and practicality of the selection method.     

Remediation of MTBE-Contaminated Water and Soil

As the number of leaking underground fuel tank sites with methyl tertiary butyl ehter (MTBE) contamination continues to grow, there is a need to develop cost-effective solutions for treatment of soil and water contamination. MTBE poses special challenges because of its physicochemical properties, in particular high solubility and low Henry's constant, low affinity for sorption, and very slow rate of microbial degradation. Advanced oxidation processes tend to generate undesirable by-products. Based on laboratory studies with hollow fiber membranes (HFM), a field-scale unit was constructed and tested at a number of sites, to determine the effectiveness of this technology in dealing with MTBE contamination. In addition, to treat the soil contamination, the HFM unit was coupled with a Spray Aeration Vapor Extraction (SAVE) unit, which is based on an internal combustion engine. The engine provides the means to treat soil vapors, as well as organic vapors from the spray aeration and HFM units. The overall treatment objectives of 5μg/l for MTBE and 1 μg/l for benzene were achieved with a treatment train consisting of an ion exchange unit, a spray aeration system, a hollow fiber membrane module and two granular activated carbon (GAC) units, for flowrates ranging from 3.8 to 30 l/min (1 to 8 gal/min). The ion exchange unit sewed to reduce water hardness and avoid scaling in the subsequent treatment units, extending the run-time of the entire system. Overall removal efficiencies for the spray aeration system and hollow fiber membrane module ranged from 85 to over 99 percent. High removal efficiencies (> 97%) were obtained at elevated water temperatures (54°C) or lower flowrates (up to 11 l/min). The GAC units were used only to polish the effluent and meet the discharge requirements. Soil, water, and gas phases are treated with this system. Cost estimates are provided for similar treatment processes, for water flowrates up to 38 l/min (10 gal/min). © 1999 John Wiley & Sons, Inc.     

Bioventing of No. 2 Fuel Oil: Effects of Air Flowrate,Temperature, Nutrient Amendment,and Acclimation

A 14‐month pilot‐scale bioventing study, sponsored by the New Hampshire Department of Environmental Services, was conducted by the University of New Hampshire to determine the effects of the time between the contamination event and the onset of bioventing, as well as air flowrate, temperature, and nutrient amendments. Freshly contaminated soil was not readily amenable to bioventing. Bioventing was effective (82–92.5 percent removal) for acclimated soil amended with nutrients at 10 °C and 20 °C for the 275 cm³/min and 140 cm³/min air flowrates, respectively. First order degradation rates after nutrient addition were ?6.11 ± 0.83 (×10^?3)/day and ?6.57 ± 1.71 (×10^?3)/day, respectively. The results indicate that bioventing will be best applied when the contamination has occurred at least two years before the onset of treatment. © 2014 Wiley Periodicals, Inc.     

Determination of suitable TPH remediation approach via MANOVA and inferential statistics assessment

Soil contamination resulting from petroleum hydrocarbon contaminants poses a fairly substantial hazard to human health and the environment. Phytoremediation, land farming, and chemico–biological stabilization were used to treat total petroleum hydrocarbons (TPHs) and polycyclic aromatic hydrocarbons (PAHs) at a crude oil polluted soil site in Nigeria. A field pilot study was conducted by preparing nine cells with subcells attached to each serving as a control with an overall area of 1.53 m². A complete block design method was used for the study. The prepared soil sample cells were divided into three groups with each group having approximately 300 kg of soil and delineated as low, medium, and high test plots. The low samples were spiked with 6.1 kg of crude oil, the medium samples were spiked with 12.2 kg of crudeoil, and the high samples were spiked with 18.3 kg of crude oil. Each row containing three cells with low, medium, and high concentrations were treated separately using the three treatment methods. The ratio of the soil sample to the organic amendment for the treatments was 2:1. The results showed over 90% degradation in the initial concentration of TPH and PAHs across different contaminant levels except in the control subcells where only 30% of degradation was recorded. Multivariate analysis of variance was employed to assess the significant difference in each treatment group while inferential statistics using a mean performance plot was used to ascertain the optimum treatment method. Land farming, chemico–biological stabilization, and phytoremediation ranked 1, 2, and 3, respectively. In conclusion, the three treatment methods employed all degraded the contaminants (TPH and PAHs) with land farming emerging as the best method.     

Dynamic workplans and field analytics: Metals assessment by inductively coupled plasma/optical emission spectroscopy

Hazardous waste site investigations were carried out at the Marine Corps Air Station (MCAS) in Yuma, Arizona and at Hanscom Air Force Base (HAFB) in Bedford, Massachusetts. The purpose of the first was to determine the location and extent of metals contamination throughout the base. The objective of the second was to evaluate the risk of metals contamination to groundwater from soil at three locations within the airfield. Dynamic workplans were developed and an adaptive sampling and analysis plan carried out with the data produced in the field used to support the goals of each project. An inductively coupled plasma/optical emission spectrometer (ICP/OES) was modified for field operation. A more efficient microwave digestion method and pressurized Teflon filtration system were developed for the HAFB project. Results were comparable to standard Environmental Protection Agency (EPA) methods, which must rely on two digestion procedures to recover EPA-targeted metals within the prescribed recovery range. The MCAS investigation, conducted over a five-month period, advanced the Navy's efforts from 30 months behind schedule to 18 months ahead of schedule, while the data generated at HAFB showed no risk to groundwater from metals.     

Triad case study: Former small arms training range

The U.S. Army Corps of Engineers (US ACE) used the Triad approach to expedite site characterization of contaminated soil at the Former Small Arms Evergreen Infiltration Training Range in Fort Lewis, Washington. The characterization was designed to determine if surface soils contain significant concentrations of metals, with the focus on collecting sufficient data for determining appropriate future actions (i.e., risk analysis or soil remediation). A dynamic sampling and analytical strategy based on rapid field‐based analytical methods was created in order to streamline site activities and save resources while increasing confidence in remediation decisions. Concurrent analysis of soil samples during the demonstration of method applicability (DMA) used both field portable X‐ray fluorescence (FPXRF) and laboratory methodologies to establish a correlation between FPXRF and laboratory data. Immediately following the DMA, contaminated soil from the impact berm was delineated by collecting both FPXRF data and fixed laboratory confirmation samples. The combined data set provided analytical results that allowed for revisions to the conceptual site model for the range and directed additional sample collection activities to more clearly determine the extent and distribution of soil contamination. © 2004 Wiley Periodicals, Inc.     

Regional Assessment of Nutrient and Pesticide Leaching in the Vegetable Production Area of Rattaphum Catchment, Thailand

Regional groundwater vulnerability maps to indicate the impact of leaching of chemicals under different management scenarios were prepared for the Rattaphum Catchment using several leaching models and GIS techniques. The Attenuation Factor (AF) model was used to simulate the leaching potential of several pesticides for selected soils in the catchment under different rates of recharge from irrigation. The LEACHN model was used to simulate the NO₃ ⁻ leaching potential and LEACHP was used to simulate leaching potential of metolachlor under different management scenarios. The results showed that only a small number of pesticides have the potential to contaminate the shallow groundwater. However, the risk of contamination with nutrients is much higher due to the mobility and conservative nature of the NO₃ ⁻. The LEACHP results indicated that the intensive use of agrochemicals in the vegetable growing area, especially during the rainy season when the groundwater is near the surface, increases the risk of pesticide contamination. The results of upscaling from the farm to the catchment scale using soil maps and GIS techniques under various management scenarios and chemical application rates showed that the most effective strategy to reduce chemical leaching is by reducing pesticide application rates and optimizing the application of irrigation water. The identification of potential high risk farms by ranking soils and agricultural practices could be used to formulate management practices that reduce pesticide contamination of the surface and ground water resources in the area.     

Residential vapor‐intrusion evaluation: Long‐duration passive sampling vs. short‐duration active sampling

Sampling indoor air for potential vapor‐intrusion impacts using current standard 24‐hour sample collection methods may not adequately account for temporal variability and detect contamination best represented by long‐term sampling periods. Henry Schuver of the U.S. Environmental Protection Agency Office of Solid Waste stated at the September 2007 Air & Waste Management Association vapor‐intrusion conference that the US EPA may consider recommending longer‐term vapor sampling to achieve more accurate time‐weighted‐average detections. In November 2007, indoor air at four residences was sampled to measure trichloroethene (TCE) concentrations over short‐ and long‐duration intervals. A carefully designed investigation was conducted consisting of triplicate samplers for three different investigatory methods: dedicated 6‐liter Summa canisters (US EPA Method TO‐15), pump/sorbent tubes (US EPA Method TO‐17), and passive diffusion samplers (MDHS 80). The first two methods collected samples simultaneously for a 24‐hour period, and the third method collected samples for two weeks. Data collected using Methods TO‐15 (canisters) and TO‐17 (tubes) provided reliable short‐duration TCE concentrations that agree with prior 24‐hour sampling events in each of the residences; however, the passive diffusion samplers may provide a more representative time‐weighted measurement. The ratio of measured TCE concentrations between the canisters and tubes are consistent with previous results and as much as 28.0 μg/m³ were measured. A comparison of the sampling procedures, and findings of the three methods used in this study will be presented. © 2008 Wiley Periodicals, Inc.     

Passive to active tie‐in for soil gas surveys: Improved technique for source‐area,spatial variability,remediation‐monitoring,and vapor‐intrusion assessment

The mass‐to‐concentration tie‐in (MtoC Tie‐In) correlates passive soil gas (PSG) data in mass to active soil gas data in concentration determined by the US EPA Method TO‐17 or TO‐15. Passive soil gas surveys consist of rapid deployment of hydrophobic sorbents (dozens to several hundred locations typically installed in one day) to a depth of six inches to three feet in a grid pattern with exposure in the field from three days to two weeks to target a wide variety of organic compounds. A power function is used on a compound‐to‐compound basis to correlate spatially varying mass (nanograms) from selected locations within a passive soil gas survey to concentration (µg/m³) at those same locations. The correlation from selected PSG locations is applied to the remainder of the PSG grid. The MtoC Tie‐In correlations provide added value to a PSG survey, with the PSG data then used to estimate risk throughout the limits of the investigation for quantitative assessment. The results from a site in northern California show the MtoC Tie‐In correlations for both benzene and total petroleum hydrocarbons (TPH). The correlations are applied on a compound‐to‐compound basis to the remaining locations in the PSG grid to provide an estimate of concentration that can be used for comparison to risk/screening levels or fate‐and‐transport diagnostic tools (partitioning equations, solubility laws, etc.). An example of how the correlations are applied is presented in tabular form. The results from a chlorinated solvent survey show the MtoC Tie‐In correlation from a site in Maryland for tetrachloroethene (PCE). In this instance, there was a near‐perfect relationship between the PSG mass and the active soil gas concentration (R² value of 1). The concentration estimated throughout a PSG grid enables a vast new realm of interpretive power at sites. Several other sites are discussed, including an example application for groundwater. © 2009 Wiley Periodicals, Inc.     

Effects of Acidification and its Mitigation with Lime and Wood Ash on Forest Soil Processes in Southern Sweden. A Joint Multidisciplinary Study

A joint multidisciplinary investigation was undertaken to studythe effects of lime and wood ash applications on two Norway spruce forest Spodosolic soils. The two sites, typical for southern Sweden, were treated in 1994 with either 3.25 t ha^-1 dolomite or 4.28 t ha^-1 wood ash (Horröd site) or in 1984 with either 3.45 or 8.75 t ha^-1 dolomite (Hasslöv site). Both sites show signs of acidification by atmospheric anthropogenic deposition and possessed low soil pH(4.3) and high concentrations of inorganic Al (35 M) in theupper illuvial soil solution. The prevailing soil conditions indicated perturbed soil processes. Following treatment with lime or wood ash, the soil conditions were dramatically altered. Cation exchange capacity (CEC) and base saturation (BS) was considerable increased after addition. Four years after application most of the added Ca and Mg was still present in the mor layer. Fifteen years after application,Mg in particular, became integrated deeper in the soil profile with a greater proportion lost by leaching incomparison to Ca. The concentrations of these ions were greatestin the mor layer soil solutions and Mg had higher mobility givinghigher concentrations also deeper in the profile. Four years after treatment, the application of wood ash and limeresulted in lower pH values and higher inorganic Al in mineral subsoil solutions compared to the untreated soil. We hypothesize that this was probably due to an increased flow of hydrogen ionsfrom the upper soil as a result of displacement by Ca and Mg ionsin the enlarged exchangeable pool. In contrast, fifteen years after lime and wood ash application, the mineral subsoil horizonspossessed a higher pH and lower soil solution Al content than theuntreated plots.Liming promoted soil microbial activity increasing soil respiration 10 to 36%. This is in the same range as net carbon exchange for forests in northern Sweden and could potentially have a climatological impact. The turnover of low molecularweight organic acids (LMWOA) by the soil microbial biomass werecalculated to contribute 6 to 20% to this CO₂ evolution.At Horröd, citrate and fumarate were the predominant LMWOAs with lowest concentrations found in the treated areas. In contrast, at the Hasslöv site, propionate and malonate were the most abundant LMWOAs. Higher microbial activity in the upper soil horizons was also theprobable cause of the considerably higher DOC concentrations observed in the soil solution of ash and lime treated areas. Thelime-induced increase in DOC levels at Hasslöv could be attributed to increases in the 3–10 kDa hydrophobic size fraction. Liming also promoted nitrification with high liming doses leading to extreme concentrations of NO₃ ^- (1 mM) in soil solution.At Hasslöv the community of mycorrhizal fungi was dramatically changed by the addition of lime, with only four of 24 species recorded being common to both control and treated areas.Many of the observed effects of lime and ash treatment can be viewed as negative in terms of forest sustainability. After fouryears of treatment, there was a decrease in the pH of the soil solution and higher concentrations of inorganic Al and DOC. Increased organic matter turnover, nitrification and NO₃ ^-leakage were found at Hasslöv. Considering that the weathering rate and the mineral nutrient uptake by trees is mostprobably governed by mycorrhizal hyphae etchingmineral grains in the soil, it is important to maintain this ability of the mycorrhizal fungi. The lime and ash-induced changed mycorrhizal community structure may significantly affect this capability. In light of this investigation and others, as reviewed by Lundström et al. (2003), the implications ofliming on forest health are multifaceted with complex relationships occurring over both space and time.     

Land treatment and the toxicity response of soil contaminated with wood preserving waste

Soils contaminated with wood preserving wastes, including pentachlo-rophenol (PCP) and creosote, are treated at field-scale in an engineered prepared-bed system consisting of two one-acre land treatment units (LTUs). The concentration of selected indicator compounds of treatment performance included PCP, pyrene, and total carcinogenic polycyclic aromatic hydrocarbons (TCPAHs) was monitored in the soil by taking both composited soil samples at multiple points in time, and discrete soil samples at two points in time. The mean concentration of the indicator compounds and the 95-percent confidence interval (CI) of the composite and discrete samples agreed relatively well, and first-order degradation rate kinetics satisfactorily represented the mean chemical concentration loss of indicator compounds in the LTU. Toxicity of the soil, as measured by Microtox^TM assay of the soil extracts, indicated that toxicity reduction corresponded with indicator compound disappearance. No toxicity effects were observed with time in treated layers of soil (lifts) buried beneath highly contaminated lifts of newly applied soil. This indicated that vertical migration of soluble contaminants from such lifts had little effect on the microbial activity in the underlying treated soil.     

Adaptive sampling and analysis programs for contaminated soils

Adaptive sampling and analysis programs (ASAPs) provide a cost-effective alternative to traditional sampling program designs. ASAPs are based on field analytical methods for rapid sample turnaround and field-based decision support for guiding the progress of the sampling program. One common objective of ASAPs is to delineate contamination present in soils, either to support feasibility studies or remedial action designs. An ASAP based on portable gas chromatograph/ mass spectrograph (GC/MS) technologies developed at Tufts University combined with decision support tools created at Argonne National Laboratory was used to delineate explosives contamination in soils at Joliet Army Ammunition Plant, Joliet, Illinois. Tufts' GC/MS technologies provided contaminant-specific identification and quantification with rapid sample turnaround and high sample throughput. Argonne's decision support tools estimated contamination extent, determined the uncertainty associated with those estimates, and indicated where sampling should continue to minimize uncertainty. In the case of Joliet, per sample analytical costs were reduced by 75 percent as compared to the cost of off-site laboratory analyses for explosives. The use of an ASAP resulted in a much more accurate identification and delineation of contaminated areas than a traditional sampling program would have with the same number of samples collected on a regular grid. While targeting explosives contamination in soils at Joliet, the ASAP technologies used in this demonstration have much broader application.     

Concentrations and Pools of Heavy Metals in Urban Soils in Stockholm,Sweden

The concentrations of heavy metals (Cd, Cr, Cu, Hg, Ni, Pb andZn) and arsenic (As) were surveyed and the metal pools estimatedin soils in Stockholm Municipality. The sampling sites were distributed all over the entire municipality with a higher sampling density in the city centre. Soils were sampled to a maximum depth of 25 to 60 cm. Soil texture, total-C content, electrical conductivity and pH were analysed. Heavy metal concentrations were determined after wet digestion with boiling7 M HNO₃.The results showed a wide range in heavy metal concentrations, as well as in other soil properties. The city centre soils constituted a rather homogeneous group whereas outside this areano geographical zones could be distinguished. These soils were grouped based on present land use, i.e. undisturbed soils, public parks, wasteland (mainly former industrial areas), and roadside soils. The city centre and wasteland soils generally hadenhanced heavy metal concentrations to at least 30 cm depth compared to park soils outside the city centre and rural (arable)soils in the region, which were used to estimate background levels. For example, the mean Hg concentration was 0.9 (max 3.3)mg kg^-1 soil at 0–5 cm and 1.0 (max 2.9) at 30 cm depth in the city centre soils, while the background level was 0,04 mg kg^-1. Corresponding values for Pb were 104 (max 444) and135 (max 339) mg kg^-1, at 0–5 and 30 cm, respectively, while the background level was 17 mg kg^-1.The average soil pools (0–30 cm depth) of Cu, Pb and Zn were 21,38 and 58 g m^-2 respectively, which for Pb was 3–4 timeshigher and for Cu and Zn 1.5–2 times higher than the backgroundlevel. The total amount of accumulated metals (down to 30 cm)in the city centre soils (4.5^*10 ⁶ m² public gardens and green areas) was estimated at 80, 1.1, 120 and 40 t for Cu, Hg, Pb and Zn, respectively. The study showed (1) thatfrom a metal contamination point of view, more homogeneous soilgroups were obtained based on present land use than on geographicdistance to the city centre, (2) the importance of establishing a background level in order to quantify the degree of contamination, and (3) soil samples has to be taken below the surface layer (and deeper than 30 cm) in order to quantify theaccumulated metal pools in urban soils.     

ERI evaluation of injectates used at a dry‐cleaning site

A former dry‐cleaning site in Jackson, Tennessee, has undergone remediation to treat dense nonaqueous‐phase liquid (trichloroethene [TCE] and tetrachloroethene [PCE]) contamination in the subsurface. The dry cleaning operation closed in 1977. In 2002, a series of injections were made at the site consisting of corn syrup, vegetable oils, and Simple Green®. In 2004, approximately 200 cubic yards of contaminated soil were excavated, and the bottom of the excavation was covered with sodium lactate. In 2009, the site was characterized using proprietary electrical resistivity imaging (ERI; commercially available as Aestus GeoTrax Surveys^TM). Follow‐up confirmation soil borings targeted anomalies detected via the geophysical work. The results indicate an extremely electrically conductive (less than 1 ohm‐m) vadose zone downgradient from the injection wells, and extremely electrically resistive areas (greater than 10,000 ohm‐m) in the phreatic zone near the injection area. The sample data indicate that the electrically resistive anomalous zones contain moderate to high concentrations of undegraded dry‐cleaning compounds. Electrically conductive anomalous zones are interpreted to be areas of biological activity generated by the amendments injected into the subsurface based on the extreme conductivity values detected, the chemical composition (i.e., PCE degradates are present), and the dominant vadose‐zone location of the conductive zones. © 2012 Wiley Periodicals, Inc.     

Natural attenuation of chlorinated solvent plumes at Texas dry cleaners

Dry cleaners are the largest users of perchloroethene (PCE) solvents in the United States. Releases from dry cleaners to soil and groundwater, however, remain largely unstudied. This article presents a database of 137 chlorinated solvent plumes at dry cleaners in Texas. The data indicate that PCE plumes are generally shorter in extent than those from industrial sites. Degradation products were observed at more than 80 percent of the sites with groundwater contamination. Calculated attenuation rates are on the order of one‐to‐three‐year half‐lives for PCE and its degradation products. The estimated cleanup timeframe for calculated attenuation rates is < 50 years. More research is needed to understand the presence of organic carbon sources at dry cleaners and its implications for natural attenuation. © 2004 Wiley Periodicals, Inc.