Noninvasive characterization of the Trecate (Italy) crude-oil contaminated site: links between contamination and geophysical signals

The characterization of contaminated sites can benefit from the supplementation of direct investigations with a set of less invasive and more extensive measurements. A combination of geophysical methods and direct push techniques for contaminated land characterization has been proposed within the EU FP7 project ModelPROBE and the affiliated project SoilCAM. In this paper, we present results of the investigations conducted at the Trecate field site (NW Italy), which was affected in 1994 by crude oil contamination. The less invasive investigations include ground-penetrating radar (GPR), electrical resistivity tomography (ERT), and electromagnetic induction (EMI) surveys, together with direct push sampling and soil electrical conductivity (EC) logs. Many of the geophysical measurements were conducted in time-lapse mode in order to separate static and dynamic signals, the latter being linked to strong seasonal changes in water table elevations. The main challenge was to extract significant geophysical signals linked to contamination from the mix of geological and hydrological signals present at the site. The most significant aspects of this characterization are: (a) the geometrical link between the distribution of contamination and the site’s heterogeneity, with particular regard to the presence of less permeable layers, as evidenced by the extensive surface geophysical measurements; and (b) the link between contamination and specific geophysical signals, particularly evident from cross-hole measurements. The extensive work conducted at the Trecate site shows how a combination of direct (e.g., chemical) and indirect (e.g., geophysical) investigations can lead to a comprehensive and solid understanding of a contaminated site’s mechanisms.     

Evaluating LNAPL contamination using GPR signal attenuation analysis and dielectric property measurements: practical implications for hydrological studies

Groundwater and sub-surface contamination by Light Non-Aqueous Phase Liquids (LNAPLs) is one of the industrial world's most pressing environmental issues and a thorough understanding of the hydrological, physical and bio-chemical properties of the sub-surface is key to determining the spatial and temporal development of any particular contamination event. Non-invasive geophysical techniques (such as electrical resistivity, electromagnetic conductivity, Ground-Penetrating Radar, etc.) have proved to be successful sub-surface investigation and characterisation tools with Ground-Penetrating Radar (GPR) being particularly popular. Recent studies have shown that the spatial/temporal variation in GPR signal attenuation can provide important information on the electrical properties of the sub-surface materials that, in turn, can be used to assess the physical and hydrological nature of the pore fluids and associated contaminants. Unfortunately, a high percentage of current LNAPL-related GPR studies focus on contaminant mapping only, with little emphasis being placed on characterising the hydrological properties (e.g., determining contaminant saturation index, etc.). By comparing laboratory-based, dielectric measurements of LNAPL contaminated materials with the GPR signal attenuation observed in both contaminated and 'clean' areas of an LNAPL contaminated site, new insights have been gained into the nature of contaminant distribution/saturation and the likely signal attenuation mechanisms. The results show that, despite some practical limitations of the analysis technique, meaningful hydrological interpretations can be obtained on the contaminant properties, saturation index and bio-degradation processes. A generalised attenuation/saturation model has been developed that describes the physical and attenuation enhancement characteristics of the contaminated areas and reveals that the most significant attenuation is related to smeared zone surrounding the seasonally changing water table interface. It is envisaged that the model will provide a basis for the interpretation of GPR data from analogous LNAPL contaminated sites and provide investigators with an appreciation of the merits and limitations of GPR-based, attenuation analysis techniques for hydrological applications.     

Non-intrusive characterization of the redox potential of landfill leachate plumes from self-potential data

Contaminant plumes (e.g., associated with leakages from municipal landfills) provide a source of natural electrical potentials (or "self-potentials") recordable at the Earth's surface. One contribution to these self-potentials is associated with pore water flow (i.e., the "streaming potential"), and the other is related to redox conditions. A contaminant plume can be regarded as a "geobattery": the source current potentially results from the degradation of the organic matter by micro-organisms, which produces electrons. These electrons are then carried by nanowires that connect bacteria and thorough metallic particles that precipitate in areas of strong redox potential gradient. In the case of the Entressen landfill (South of France), reported here, the hydraulic head differences measured in piezometers outside the contaminant plume is strongly linked to the surface self-potential signals, with a correlation coefficient of -0.94. We used a Bayesian method that combines hydraulic head and self-potential data collected outside the contaminated area to estimate the streaming potential component of the collected self-potential data. Once the streaming potential contribution was removed from the measured self-potentials, the correlation coefficient between the residual self-potentials and the measured redox potentials in the aquifer was 0.92. The slope of this regression curve was close to 0.5, which was fairly consistent with both finite element modelling and the proposed geobattery model.     

Monitoring microbial community in a subsurface soil contaminated with hydrocarbons by quinone profile

A natural attenuation experiment was carried out using a lysimeter for 308 days after contaminating the subsoil with hydrocarbons (HCs) and the changes in the structures of microbial community in the hydrocarbon (HC) contaminated subsoil were monitored by quinone profile analysis. The residues of HCs remained for 217 days in the subsoil after the contamination. The amount of total quinones (TQ), an indicator of microbial biomass, significantly increased in the HC contaminated subsoil for 217 days, comparing with that of the background subsoil or the subsoil before the addition of HCs. The major quinone species and the quinone composition, indicators of community structure, were significantly different between the HC contaminated soil and the background soil for 217 days. The major increased quinine species in the HC contaminated soil were menaquinone-8(H4), menaquinone-9(H2) and ubiquinone-9, indicating the propagation of Gram-positive bacteria with high guanine and cytosine content and gamma-subclass of Proteobacteria and fungi. There was no significant difference in the diversity of the quinone species (DQ), an indicator of taxonomic diversity of microbial community, except for the decrease in DQ in the shallow subsoil after 35 days when a high concentration of HCs was detected. After 308 days when the HCs in the subsoil disappeared, TQ returned to the level of the background soil, and no significant difference in quinone composition were observed between the HC contaminated soil and the background soil. The results suggested that respiratory quinones are effective biomarkers for characterizing the temporal changes of microbial community in the HC contaminated subsoil.     

Organochlorinated pesticides, PCBs, dioxins, and PBDEs in grey mullets (Liza ramada) and allis shads (Alosa alosa) from the Vilaine estuary (France)

This study aimed to compare the contamination levels of various organohalogenated compounds in two migratory fish species in the Vilaine River in western France. Organochlorinated pesticides, polychlorinated biphenyls (PCBs), dioxins (polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDDs/Fs)), and polybrominated diphenyl ethers (PBDEs) were analyzed in two diadromous species from the Vilaine estuary, the grey mullet (Liza ramada)—an amphihaline species, and the allis shad (Alosa alosa)—an anadromous species. Fish were collected in spring 2004 and spring 2005, upstream and downstream of the Arzal Dam. PCB contamination varied from 27 to 200 ng?g^?1 dry weight (d.w.). PCDDs/Fs, expressed in toxicity equivalent quantity (TEQ) varied from 0.4 to 2.8 pg?g^?1 d.w. Dioxins and dioxin-like PCBs expressed in total TEQ varied from 1.4 to 18.8 pg?g^?1 d.w. PBDE47 was present at around 2–10 ng?g^?1 d.w. and concentrations of the insecticide dichlorodiphenyltrichloroethane breakdown product p,p′-dichlorodiphenylchloroethylene varied from 1 to 14 ng?g^?1 d.w. For both species, specimens collected upstream were more contaminated. The grey mullet specimens were less contaminated than the allis shad when taken downstream of the dam but were more contaminated upstream. The allis shads presented intermediate contaminant concentrations with a less pronounced difference between upstream and downstream specimens. However, it is thought that shads do not feed when they spawn in the upstream parts of rivers, which should modify the contaminant concentrations. However, measurements in upstream shad samples show an unexpected increase of the contamination, which remains unexplained.     

Hematological and histopathological changes in silver catfish Rhamdia quelen (Siluriformes) exposed to clomazone herbicide in the Madre River,Santa Catarina State,Southern Brazil

This study evaluated the influence of the clomazone herbicide (2-[(2-chlorophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone) contamination on the hematological parameters and histological changes in gills and liver of silver catfish (Rhamdia quelen) from Madre River, Santa Catarina State, Southern Brazil. Fish were collected between March 2010 and January 2012 at two different sites of the Madre River, one site receiving residual water (contaminated site) from rice culture (n = 49) and another that do not receive residual water (reference site) (n = 48). The herbicide clomazone analysis detected 3.40 ± 1.70 μg/L in the contaminated site and 1.1 ± 0.33 μg/L in the reference site. Fish from contaminated site showed increased (P < 0.05) number of monocytes suggesting the possible defense response as a result of chronic exposure to clomazone. On the other hand, no difference was found in the hematocrit percentage, red blood cell count, total thrombocyte number, white blood cell count, lymphocytes, and neutrophils number. Fish from both sites showed histopathological changes in gills and liver, possibly caused by chronic exposure to contamination. The influence of herbicide sub doses on fish health is also discussed.     

Temporal trends of polycyclic aromatic hydrocarbons (PAHs) in Dreissena polymorpha specimens from Lake Maggiore (Northern Italy)

The Lake Maggiore (Northern Italy) has been recognized as an aquatic environment heavily contaminated by persistent organic pollutants, mainly organochlorine compounds, but to date limited information is available regarding another class of widespread and hazardous pollutants, such as the polycyclic aromatic hydrocarbons (PAHs). The aim of this study was to investigate seasonal and temporal trends of 18 PAHs accumulated in native Dreissena polymorpha specimens during a 5-year biomonitoring program, as well as to identify the possible PAH emission sources by using isomeric diagnostic ratios. Zebra mussels were sampled both in their pre- (May) and post-reproductive (September) stage over the 2008–2012 period in eight sampling stations covering the whole lake shoreline. PAH concentrations were measured through gas chromatography coupled to mass spectrometry. A notable PAH contamination following an increasing temporal trend was noticed in bivalves from all the sampling stations, with the benzo(α)anthracene as the predominant compound. An overall increase in PAH levels was found in the post-reproductive surveys, indicating a marked seasonality of this contamination probably due to the increase in touristic activity during spring–summer months.     

Contamination status of arsenic and other trace elements in drinking water and residents from Tarkwa, a historic mining township in Ghana

This study was conducted to assess the contamination status of 22 trace elements, especially As in water and residents in Tarkwa, a historic mining town in Ghana. Drinking water and human urine samples were collected from Tarkwa in addition to control samples taken from Accra, the capital of Ghana in March, 2004. Concentrations of As and Mn in some drinking water samples from Tarkwa were found above the WHO drinking water guidelines posing a potential health risk for the people. A potential health risk of As and Mn is a concern for the people consuming the contaminated water in this area. No significant difference of As concentrations in human urine between mining town (Tarkwa) and control site (Accra) was observed. Although As concentrations in drinking water in Tarkwa were low, urinary As levels were comparable to those reported in highly As-affected areas in the world. These results suggest the presence of other sources of As contamination in Ghana. This is the first study on multi-elemental contamination in drinking water and human from a mining town in Ghana.     

Life cycle of PCBs and contamination of the environment and of food products from animal origin

This report gives a summary of the historic use, former management and current release of polychlorinated biphenyls (PCBs) in Germany and assesses the impact of the life cycle of PCBs on the contamination of the environment and of food products of animal origin. In Germany 60,000 t of PCBs were used in transformers, capacitors or as hydraulic oils. The use of PCB oils in these “closed applications”, has been banned in Germany in 2000. Thirty to 50% of these PCBs were not appropriately managed. In West Germany, 24,000 t of PCBs were used in open applications, mainly as additive (plasticiser, flame retardant) in sealants and paints in buildings and other construction. The continued use in open applications has not been banned, and in 2013, an estimated more than 12,000 t of PCBs were still present in buildings and other constructions. These open PCB applications continuously emit PCBs into the environment with an estimated release of 7–12 t per year. This amount is in agreement with deposition measurements (estimated to 18 t) and emission estimates for Switzerland. The atmospheric PCB releases still have an relevant impact on vegetation and livestock feed. In addition, PCBs in open applications on farms are still a sources of contamination for farmed animals. Furthermore, the historic production, use, recycling and disposal of PCBs have contaminated soils along the lifecycle. This legacy of contaminated soils and contaminated feed, individually or collectively, can lead to exceedance of maximum levels in food products from animals. In beef and chicken, soil levels of 5 ng PCB-TEQ/kg and for chicken with high soil exposure even 2 ng PCB-TEQ/kg can lead to exceedance of EU limits in meat and eggs. Areas at and around industries having produced or used or managed PCBs, or facilities and areas where PCBs were disposed need to be assessed in respect to potential contamination of food-producing animals. For a large share of impacted land, management measures applicable on farm level might be sufficient to continue with food production. Open PCB applications need to be inventoried and better managed. Other persistent and toxic chemicals used as alternatives to PCBs, e.g. short chain chlorinated paraffins (SCCPs), should be assessed in the life cycle for exposure of food-producing animals and humans.     

A comparative assessment of heavy metal accumulation in soft parts and byssus of mussels from subarctic, temperate, subtropical and tropical marine environments

Existing data on metal concentrations in mussels from subarctic, temperate, subtropical and tropical waters were analyzed using multivariate statistics in order to assess regional variations in metal contamination. Potential errors were reduced by only analyzing data from surveys that employed the same protocols, analytical methodologies and analysts. Factor analysis demonstrated that mussels inhabiting extremely contaminated areas (e.g. from Japanese and Swedish metallurgy sources) could be separated from mussels from other contaminated areas, and that metals such as Cd, Pb, Cu and Zn could be used to identify heavily contaminated samples while Co, Fe, Cr and Ni concentrations were good markers for exposure to inputs from different industrial sources. Furthermore byssus, like soft tissue, selectively and sensitively reflects variations of certain metal concentrations in ambient waters and thus serves as a reliable biomonitor for these contaminants in a variety of coastal and estuarine areas.     

Metal uptake capability of <Emphasis Type="Italic">Cyperus articulatus</Emphasis> L. and its role in mitigating heavy metals from contaminated wetlands

Wetland plants are biological filters that play an important role in maintaining aquatic ecosystem and can take up toxic metals from sediments and water. The present study investigated the seasonal variation in the accumulation potential of heavy metals by Cyperus articulatus in contaminated watercourses. Forty quadrats, distributed equally in 8 sites (six contaminated sites along Ismailia canal and two uncontaminated sites along the River Nile), were selected seasonally for sediment, water, and plant investigations. Autumn was the flourishing season of C. articulatus with the highest shoot density, length, and diameter as well as aboveground biomass, while summer showed the least growth performance. The photosynthetic pigments were markedly reduced under contamination stress. C. articulatus plants accumulated concentrations of most heavy metals, except Pb, in their roots higher than the shoots. The plant tissues accumulated the highest concentrations of Fe, Cd, Ni, and Zn during autumn, while Cu and Mn during spring, and Cr and Co during winter. It was found that Cd, Cu, Ni, Zn, Pb, and Co had seasonal bioaccumulation factor (BF) > 1 with the highest BF for Cd, Ni, and Zn during autumn, Co, Cu, and Pb in winter, spring, and summer, respectively. The translocation factor of most heavy metals, except Pb in spring, was <1 indicating potential phytostabilization of these metals. In conclusion, autumn is an ideal season for harvesting C. articulatus in order to monitor pollution in contaminated wetlands.     

Spatial and temporal trends in surface water and sediment contamination in the Laurentian Great Lakes

Data from recent sediment and surface water surveys have been collated and mapped to illustrate the spatial distribution of contaminants across the entire Great Lakes basin. Information from historical surveys, together with data from surface water monitoring programs in three major connecting channels, has also been collated in order to evaluate temporal trends. In general, Lakes Superior and Michigan exhibited the lowest levels of sediment contamination while Lake Ontario had the highest. Contaminants such as gamma-HCH (lindane) and dieldrin were ubiquitous in surface waters across the entire basin, which was indicative of atmospheric sources. The distribution of other compounds including hexachlorobenzene, octachlorostyrene and mirex indicated the presence of local sources within the watersheds of the connecting channels. Surficial sediment contamination was found to have decreased markedly since the late 1960s and 1970s. Similarly, surface water contamination decreased over the period 1986-1997 with concentrations of dieldrin, hexachlorobenzene, octachlorostyrene and mirex reduced by over 50%. However, the spatial distributions of both sediment and surface water contamination indicate that further effort is warranted in reducing local sources of contaminants, particularly in Lake Ontario.     

Ionic contribution to the self-potential signals associated with a redox front

In contaminant plumes or in the case of ore bodies, a source current density is produced at depth in response to the presence of a gradient of the redox potential. Two charge carriers can exist in such a medium: electrons and ions. Two contributions to the source current density are associated with these charge carriers (i) the gradient of the chemical potential of the ionic species and (ii) the gradient of the chemical potential of the electrons (i.e., the gradient of the redox potential). We ran a set of experiments in which a geobattery is generated using electrolysis reactions of a pore water solution containing iron. A DC power supply is used to impose a difference of electrical potential of 3 V between a working platinum electrode (anode) and an auxiliary platinum electrode (cathode). Both electrodes inserted into a tank filled with a well-calibrated sand infiltrated by a (0.01 mol L^− 1 KCl + 0.0035 mol L^− 1 FeSO₄) solution. After the direct current is turned off, we follow the pH, the redox potential, and the self-potential at several time intervals. The self-potential anomalies amount to a few tens of millivolts after the current is turned off and decreases over time. After several days, all the redox-active compounds produced initially by the electrolysis reactions are consumed through chemical reactions and the self-potential anomalies fall to zero. The resulting self-potential anomalies are shown to be much weaker than the self-potential anomalies observed in the presence of an electronic conductor in the laboratory or in the field. In the presence of a biotic or an abiotic electronic conductor, the self-potential anomalies can amount to a few hundred millivolts. These observations point out indirectly the potential role of bacteria forming biofilms in the transfer of electrons through sharp redox potential gradient in contaminant plumes that are rich in organic matter.     

Cadmium (Cd) distribution and contamination in Chinese paddy soils on national scale

Rice is a staple food by an increasing number of people in China. As more issues have arisen in China due to rice contaminated by cadmium (Cd), Cd contamination in arable soils has become a severe problem. In China, many studies have examined Cd contamination in arable soils on a national scale, but little studies have focused on the distribution of Cd in paddy fields. This study explored the spatial pattern of Cd in paddy soils in China, made a preliminary evaluation of the potential risk, and identified the most critically contaminated regions based on the domestic rough rice trade flow. The results showed that Cd concentrations in paddy soils in China ranged from 0.01 to 5.50 mg/kg, with a median value of 0.23 mg/kg. On average, the highest Cd concentrations were in Hunan (0.73 mg/kg), Guangxi (0.70 mg/kg), and Sichuan (0.46 mg/kg) provinces. Cd concentrations in paddy soils in central and western regions were higher than those in eastern regions, especially the southeastern coastal regions. Of the administrative regions, Cd standard exceedance rate was 33.2 %, and the heavy pollution rate was 8.6 %. Regarding to Cd of paddy soil, soil environmental quality was better in Northeast China Plain than in Yangtze River Basin and southeastern coastal region. Mining activities were the main anthropogenic pollution source of Cd in Chinese paddy soil. Based on rice trade, more of the Chinese population would be exposed to Cd through intake of rice produced in Hunan province. Certain regions that output rice, especially Hunan province, should be given priority in the management and control of Cd contamination in paddy soil.     

Isotopes as tracers in a contaminated fractured chalk aquitard

Clusters of industrial plants often generate contaminant plumes with several potential sources. Prevention of further pollution and designing suitable remedial measures require identification of the contributing source among all potential ones and the sorting of currently active sources from historical ones. In the study area, an industrial complex in the Negev desert, Israel, contaminants could not serve as indicators for the contamination sources because of their extensive spatial distribution across the site. However, stable isotopes of oxygen, hydrogen and sulfur, as well as tritium, proved to be efficient tools for this task. The isotopic characterization of the potential end members provided the criteria for constraining a contaminating source when several alternative sources appeared viable. The isotopic fractionation of oxygen and hydrogen isotopes could be tied to the various disposal phases of the industrial wastewater. The three case studies presented here confirm the important role of isotopes as tracers in contaminated sites.     

Polychlorinated biphenyls in sediments of the Venice Lagoon

Twenty-four surficial sediment samples, representing different environments within the Venice Lagoon, were analyzed for polychlorinated biphenyls (PCBs) in order to assess degrees of pollution, sources, areal distribution, and potential risk for the environment. Concentrations in surficial sediments range from 2 to more than 2049 microg kg(-1) dw. The maximum is probably due to the discharge of industrial wastes into the Brentella Canal, within the first Industrial Area. Lagoon samples are 11-205 times less contaminated, being influenced by pollutants stored in the canals only occasionally. Congener profiles distinguish PCBs in two main categories. The baseline pollution is probably due to a variety of sources within the lagoon system, whereas less chlorinated PCBs were discharged into the Brentella Canal. Our estimates suggest that, due to high concentrations, toxic equivalents (TEQs) of PCBs are comparable to those relative to PCDD/Fs for the least contaminated samples, whereas they are lower in case of heavy PCDD/F contamination.     

Electrical resistivity tomography as monitoring tool for unsaturated zone transport: an example of preferential transport of deicing chemicals

Non-invasive spatially resolved monitoring techniques may hold the key to observe heterogeneous flow and transport behavior of contaminants in soils. In this study, time-lapse electrical resistivity tomography (ERT) was employed during an infiltration experiment with deicing chemical in a small field lysimeter. Deicing chemicals like potassium formate, which frequently impact soils on airport sites, were infiltrated during snow melt. Chemical composition of seepage water and the electrical response was recorded over the spring period 2010. Time-lapse electrical resistivity tomographs are able to show the infiltration of the melt water loaded with ionic constituents of deicing chemicals and their degradation product hydrogen carbonate. The tomographs indicate early breakthrough behavior in parts of the profile. Groundtruthing with pore fluid conductivity and water content variations shows disagreement between expected and observed bulk conductivity. This was attributed to the different sampling volume of traditional methods and ERT due to a considerable fraction of immobile water in the soil. The results show that ERT can be used as a soil monitoring tool on airport sites if assisted by common soil monitoring techniques.     

A comprehensive investigation and assessment of mercury in intertidal sediment in continental coast of Shanghai

The aims of this paper were to survey the total Hg levels and distribution character in intertidal sediment in continental coast of Shanghai, and identify the environment factors that might influence the sediment Hg concentrations, and to assess the pollution degree and potential ecological risk of Hg in sediment. Eighty-eight surface sediment samples and 18 sediment cores were collected for Hg contamination analysis. Physicochemical properties including Eh, particle size, content of total organic carbon (TOC), and acid volatile sulfide (AVS) were also measured. Index of geo-accumulation (I _geo) and potential ecological risk index were used respectively to assess the pollution levels and the ecological risk of sediment Hg. The average of total Hg concentrations in surface sediments was 107.4?±?90.9 ng/g with the range from 0 to 465.9 ng/g. Higher Hg concentrations were generally found in surface sediments near sewage outfalls and the mouth of rivers. Total Hg concentrations were significantly correlated with TOC (p?<?0.05) both in surface (r?=?0.24) and core (r?=?0.29) sediments, but not with the other environment factors (Eh, AVS, and particle size). Geo-accumulation index indicated that Hg contamination in intertidal sediments was generally at none to moderate degree, while potential ecological risk index demonstrated that the risk caused by Hg were at moderate to considerable level. Intertidal sediment in continental coast of Shanghai has generally been contaminated by Hg, and it might pose moderate to considerable risk to the local ecosystem. The Hg contamination is related more to the coastal pollution sources and complicated hydrodynamic and sedimentary conditions than the other environment factors studied.     

Combined geospatial,geophysical and hydrochemical studies on coastal aquifer at Muttom–Mandaikadu area,Tamilnadu, India

A study was conducted in the Muttom–Mandaikadu coastal region, which is among the profitable coastal sectors in Tamil Nadu, to find the groundwater potential as well as its quality by an integrated geospatial, geophysical and geochemical approach. The GIS-based weighted overlay analysis was used to merge five thematic layers to create the groundwater potential zone map. The geophysical resistivity survey was performed in the study area at 26 stations by applying Schlumberger vertical electrical sounding technique. The observed data were inverted to develop a subsurface lithology model and its electrical properties using one-dimensional software AGI Earth Imager. The combined vertical electrical sounding result and remote sensing thematic maps have exposed the potential zone of groundwater in the study area. From the inferred results, it was observed that 20.8% of the area has ample groundwater potential and 7.7% of the area has scanty groundwater potential. The saltwater intrusion zone had been predicted by validating aquifer resistivity with Dar-Zarrouck (D-Z) parameter. From the geophysical and geochemical interpreted results, it was found that aquifers in 34.6% of the study area are vulnerable to saline contamination. The 4-D model with integrated groundwater quantity and quality suggests that the study area's Western part falls under excellent-to-good groundwater potential zone and excellent water quality.

     

Former DDT factory in Pakistan revisited for remediation: severe DDT concentrations in soils and plants from within the area

A factory in Amman Garh near Nowshera, Khyber Pakhtunkhwa, Pakistan, produced dichlorodiphenyltrichloroethane (DDT) from 1963–1994. Consequently, earlier papers reported a soil contamination in the per mille range inside the former factory wall (88 m?×?106 m) and up to 10 mg/kg of DDT in the surroundings in 2005–2007. The site within the factory wall was remonitored systematically in 2011 to complement the earlier data as a prerequisite for remediation, to put them in exposure context in a population developing area, and to suggest and evaluate the optimal remediation technique for the site. The contamination was drastically higher than the earlier published data, and the sum of DDT and its metabolites (ΣDDT) was up to 65 % in the soil. Grasses, shrubs, and trees growing in this severely contaminated site had 50–450 mg/kg_dw of ΣDDT. Thus, people living nearby and husbandry as well as wild animals are heavily exposed to DDT. The semiarid climate favors wind drift and deposition of the pollutant. Additionally, DDT from products of herbivore animals feeding on the contaminated plants will enter the food web. To overcome the exposure and distribution of the DDT, the site within the factory wall was capped with 1.5 m of soil. This remediation technique represents the easiest and least expensive solution. Nevertheless, DDT can still evaporate or leach, and groundwater can rise in this flood-prone area and thereby become contaminated, especially because a binding layer is missing.