Screening of wood rotting fungi potentially useful for the degradation of organic pollutants

Many papers have shown that white rot fungi can degrade aromatic pollutants under laboratory conditions, but few report field scale trials. Here we report the first steps in the development of a remediation system for Greek conditions. A review of the available organochlorine compound pollution information in Greece is presented. White rot fungi isolated from sites in Greece have been screened for growth rate and ligninolytic activity, using decolourisation of the dye Poly R-478 as an indicator of enzyme activity. Use of white rot fungi under field conditions in Greece will require bioaugmentation to be effective at high temperatures and low water activity for much of the year. The most potent strains have been selected under a range of conditions and have been challenged with priority pollutants to determine their degradative ability under laboratory conditions and subsequently ex situ in soil.     

糙皮侧耳降解碱木素的动力学研究

对糙皮侧耳B1(白腐真菌的一种)降解碱木素的动力学进行了研究.基于Logistic方程,建立了糙皮侧耳B1在纯培养条件和碱木素存在条件下的生长动力学模型.动力学模型参数分别为0.94d-1和0.90d-1.该模型能够较好地模拟体系中生物量的变化,平均相对误差分别为3.2％和3.4％.糙皮侧耳B1对低浓度碱木素的降解存在...     

A Novel Approach to Biological Treatment of Contaminated Water

Over the past few years, the focus of our research has been to respond to the recognized needs for novel biological processes that are capable of destroying a wide range of biodegradable pollutants and providing the perfect environment for complex interspecies interactions required for the degradation of environmental contaminants. A new biotechnology process called Biological Permeable Barrier (BPB) was developed to provide high microbial density, stable environmental conditions, and protective measures for microbial activities for in‐situ bioremediation of contaminated groundwater. This patented technology (U.S. Patent 6,337,019 ) is based on the creation of a structured matrix, or Bio‐beads, that provides the perfect environment for organic‐degrading microorganisms to establish biofilms capable of destroying the contaminants in water with remarkable stability and control. For over 240 days, the viability and performance of the BPB (Bio‐beads) system were shown for biodegradation of a targeted contaminant, 2,4,6‐ trichlorophenol (TCP), under a variety of operating and stress conditions (Razavi‐Shirazi, 1997 ). Extensive batch experiments were also conducted to obtain necessary data to determine the rate of TCP diffusion into the Bio‐beads, adsorption properties of the Bio‐beads, and substrate‐use rate of the mixed bioculture as free cells and as immobilized cells (Bio‐beads). A simulated model of BPB was also characterized with its porosity, permeability, and compressibility or deformation under typical field conditions. Our extensive research showed that BPB takes advantage of a controlled biotechnology process to overcome the disadvantages and uncertainties associated with conventional biological processes. A summary of our investigation is presented here. © 2002 Wiley Periodicals, Inc.     

Infrared and nuclear magnetic resonance evidence of degradation in thermoplastics based on forest products

The degradation of lignin-(1-phenylethylene) graft copolymers (lignin-styrene graft copolymers) by white rot basidiomycete fungi was followed by monitoring aromatic absorption bands by Fourier transform infrared (FTIR) spectroscopy and nuclear magnetic resonance (NMR) spectroscopy. The FTIR of the graft copolymers shows a series of characteristic absorbance peaks from multi-substituted aromatic rings and a strong poly(1-phenylethylene) (polystyrene) absorbance peak from monosubstituted aromatic rings. Subtraction of copolymer spectra taken before incubation from spectra taken after 50 days of incubation with the four tested fungi shows the loss of functional groups from the copolymer. NMR spectra also show reduction of aromatic ring resonances from the copolymer and incorporation of peaks from fungi as a result of incubation with fungi. The biodegradation tests were run on lignin-(1-phenylethylene) graft copolymers which contained 10.3, 32.2, and 50.4% of lignin. The polymer samples were incubated with the white rot fungiPleurotus ostreatus, Phanerochaete chrysosporium, andTrametes versicolor, and the brown rot fungusGleophyllum trabeum. White rot fungi degraded the plastic samples at a rate that increased with increasing lignin content in the copolymer sample. Both poly(1-phenylethylene) and lignin components of the copolymer were readily degraded. Observation by scanning electron microscopy of incubated copolymers showed a deterioration of the plastic surface. The brown rot fungus did not affect any of these plastics, nor did any of the fungi degrade pure poly(1-phenylethylene).Paper presented at the Bio/Environmentally Degradable Polymer Society—Second National Meeting, August 19–21, 1993, Chicago, Illinois.     

Comparing PFAS to other groundwater contaminants: Implications for remediation

Established groundwater contaminants such as chlorinated solvents and hydrocarbons have impacted groundwater at hundreds of thousands of sites around the United States and have been responsible for multibillion dollar remediation expenditures. An important question is whether groundwater remediation for the emerging contaminant class comprised of per‐ and polyfluoroalkyl substances (PFAS) will be a smaller, similar, or a larger‐scale problem than the established groundwater contaminants. A two‐pronged approach was used to evaluate this question in this paper. First, nine quantitative scale‐of‐remediation metrics were used to compare PFAS to four established contaminants: chlorinated solvents, benzene, 1,4‐dioxane, and methyl tert‐butyl ether. These metrics reflected the prevalence of the contaminants in the U.S., attenuation potential, remediation difficulty, and research intensity. Second, several key challenges identified with PFAS remediation were evaluated to see similar situations (qualitative analogs) that have been addressed by the remediation field in the past. The results of the analysis show that four out of nine of the evaluated quantitative metrics (production, number of potential sites, detection frequency, required destruction/removal efficiency) indicate that the scale of PFAS groundwater remediation may be smaller compared to the current scale of remediation for conventional groundwater contaminants. One attenuation metric, median plume length, suggests that overall PFAS remediation could pose a greater challenge compared to hydrocarbon sites, but only slightly larger than chlorinated volatile organic compounds sites. The second attenuation metric, hydrophobic sorption, was not definitive regarding the potential scale of PFAS remediation. The final three metrics (regulatory criteria, in‐situ remediation capability, and research intensity) all indicate that PFAS remediation might end up being a larger scale problem than the established contaminants. An assessment of the evolution of groundwater remediation capabilities for established contaminants identified five qualitative analogs for key PFAS groundwater remediation issues: (a) low‐level detection analytical capabilities; (b) methods to assess the risk of complex chemical mixtures; (c) nonaqueous phase dissolution as an analog for partitioning, precursors, and back diffusion at PFAS sites; (d) predictions of long plume lengths for emerging contaminants; and (e) monitored natural attenuation protocols for other non‐degrading groundwater contaminants. Overall the evaluation of these five analogs provided some comfort that, while remediating the potential universe of PFAS sites will be extremely challenging, the groundwater community has relevant past experience that may prove useful. The quantitative metrics and the qualitative analogs suggest a different combination of remediation approaches may be needed to deal with PFAS sites and may include source control, natural attenuation, in‐situ sequestration, containment, and point‐of‐use treatment. However, as with many chlorinated solvent sites, while complete restoration of PFAS sites may be uncommon, it should be possible to prevent excessive exposure of PFAS to human and ecological receptors.     

A New Perspective on Sustainable Soil Remediation—Case Study Suggests Novel Fungal Genera Could Facilitate in situ Biodegradation of Hazardous Contaminants

Deciding upon a cost effective and sustainable method to address soil pollution is a challenge for many remedial project managers. High pressure to quickly achieve cleanup goals pushes for energy‐intensive remedies that rapidly address the contaminants of concern with established technologies, often leaving little room for research and development especially for slower treatment technologies, such as bioremediation, for the more heavily polluted sites. In this case study, new genomic approaches have been leveraged to assess fungal biostimulation potential in soils polluted with particularly persistent hydrophobic contaminants. This new approach provides insights into the genetic functions available at a given site in a way never before possible. In particular, this article presents a case study where next‐generation sequencing has been used to categorize fungi in soils from the Atlantic Wood Industries Superfund site in Portsmouth, Virginia. Data suggest that original attempts to harness fungi for bioremediation may have focused on fungal genera poorly suited to survive under heavily polluted site conditions, and that more targeted approaches relying on native indigenous fungi which are better equipped to survive under site‐specific conditions may be more appropriate. ©2016 Wiley Periodicals, Inc.     

Isolation and identification of potential fungal species for spent engine lubrication oil remediation in Peninsular Malaysia

Improper disposal and spills of spent engine oil into the environment can result in contamination, which eventually affects humans through the food chain. Mycoremediation is an effective and inexpensive alternative to clean up spent engine oil contamination. In recent work, the potential effectiveness of fungi for degrading spent engine oil was confirmed, with the species identified through molecular identification. Fungi that were able to grow in Bushnell Haas Broth supplied with spent engine oil were identified with the potential to utilize spent engine oil as a carbon source. Six species of fungi namely Penicillium simplicissimum, Aspergillus nidulans, Aspergillus niger, Trichoderma longibrachiatum, Aspergillus ustus, and Aspergillus flavus were successfully identified in this study. Over a course of seven days, P. simplicissimum (21.11 percent) was identified as the most effective fungi in degrading spent engine oil, followed by A. nidulans (17.75 percent), A. niger (15.85 percent), T. longibrachiatum (15.12 percent), A. ustus (15.02 percent), and A. flavus (11.80 percent). As these species of fungi were isolated from the natural environment in Peninsular Malaysia, the potential of using these fungi as mycoremediation of spent engine oil was therefore confirmed.     

Contribution to the Study of Fungal Attack on Some Plasticized Vinyl Formulations

The objective of this study was to develop new vinyl flooring formulations with increased resistance to fungi and microorganisms attack, by using plasticizers having a chemical composition different from that of common di-ethylhexyl phthalate (DOP). It is suspected that during the vinyl flooring life service, the attack of fungi and microorganisms leads to the degradation of DOP and the release of some volatile organic compounds (VOC). For this reason the new materials were formulated with plasticizers having chemical composition different of that of DOP i.e.: diethyleneglycol dibenzoate (2–45), tricresyl phosphate (Lindol) and phenol alkylsulphonic ester (Mesamoll). For the same reason in the new flooring formulations the vinyl polymer, vinyl chloride-vinyl acetate copolymer (VC-VAc), was partially replaced with lignin (L) a natural polymer and major component of wood and vascular plants. Besides its other functions in wood, L imparts resistance to the most microorganisms attack. An organosolv lignin Alcell lignin (AL) was utilized as partial replacement of VC-VAc copolymer.The influence of the new plasticizers, as well as the influence of the partial replacement of VC-VAc copolymer with L on the resistance of the new formulations to fungal attack was evaluated following a standard procedure given in ASTM G 21–2002 “Determining Resistance of Synthetic Polymeric Materials to Fungi”. The evaluation has been undertaken for controls (formulated without AL) and blends (formulated with 20 parts AL) specimens. Test specimens were inoculated with a mixture of five fungi. Following 28 days of incubation at 28°C and 95% relative humidity, the specimens were examinated visual and under the microscope and rated for fungal growth. Weight loss, changes in mechanical properties and changes in glass transition temperature due to the effect of biodeterioration were also determined.Although each plasticizer has a specific resistance to hydrolysis due to differences among ester groups, the visible effects of fungal attack, in formulations without AL, is similar for all plasticized controls, with the exception of formulations incorporating diethyleneglycol dibenzoate (2–45) in which a higher degree of biodegradation was always present. Based on the weight loss of specimens formulated without AL, their resistance to fungal attack can be rated as follows: . The same rating is applicable for blend specimens. The results have demonstrated that each particular AL-plasticizer-additives formulation has its specific mechanism of biodegradation.     

Styrene/Lignin-Based Polymeric Composites Obtained Through a Sequential Mass-Suspension Polymerization Process

A modified sequential mass-suspension polymerization was employed to ensure adequate dispersion of lignin into the monomeric phase. Due to its complex macromolecular structure and low compatibility with styrene, eucalyptus wood-extracted lignin, via a modified Kraft method, was esterified with methacrylic anhydride to ensure organic phase homogeneity into the reaction medium. Infrared spectroscopy showed a decrease in the hydroxyl band, a characteristic of natural lignin (3200–3400 cm^?1) and an increase in the characteristic ester band (1720–1740 cm^?1) whereas nuclear magnetic resonance measurements exhibited intense peaks in the range from 1.7 to 2.05 ppm (–CH₃) and 5.4 to 6.2 ppm (=CH₂), related to methacrylic anhydride. Comparatively, the esterified lignin also displayed an increase of its glass transition temperature for 98?°C, related to natural lignin, whose T _g was determined to be equal to 91?°C. Styrene/lignin-based polymers exhibited higher average molar masses in comparison to the values observed for polystyrene synthesized with similar amounts of benzoyl peroxide, due to the ability of lignin to act as a free-radical scavenger. Composites obtained with styrene and natural or esterified lignin were successfully synthesized, presenting regular morphology and proper lignin dispersion. Based on a very simple polymerization system, it is possible to enhance the final properties of polystyrene through the incorporation of lignin, which represents an important platform for developing attractive polymeric materials from renewable resources.     

A conceptual study on the bio-wall technology: Feasibility and process design

In-situ bioremediation is a process by which contaminants in subsurface environments are biologically eliminated or mineralized; however, it is often difficult to implement. Microbes sparsely distributed in deep soils are incapable of degrading a chemical rapidly; furthermore, fine-pore structures of soils tend to retard the penetration and propagation of these microbes and hinder oxygen transfer. The latter is particularly detrimental to the aerobic growth of microbes, which is often essential for bioremediation. Measures intended to promote bioremediation, such as the addition of surfactants for enhancing dissolution and the application of genetically engineered microbes for accelerating the biodegradation of contaminants, are almost impossible to adopt. This is attributable to the fact that various facets of the bioremediation process (e.g., the distribution of dissolved contaminants, nutrients, and oxygen, and the concentration of microbes) cannot be readily manipulated. This article proposes a novel technology, namely, bio-wall. This technology resorts to an in-situ constructed medium with porosity and organic content greater than those of the original soil for promoting the adsorption and retention of microbes and the biodegradation of contaminants. Moreover, oxygen and nutrients are supplied to the bio-wall to facilitate microbialgrowth. The results of conceptual design study and simulation have revealed that the technology is indeed feasible and, under certain environmental conditions, cost-effective. Particularly noteworthy is the fact that bio-wall can prevent contaminant migration through the enhancement of the biodegradation rate and reduction of the plume-distance, both by several orders of magnitude.     

Microbial degradation of pyridine using Pseudomonas sp. and isolation of plasmid responsible for degradation

Pseudomonas (PI2) capable of degrading pyridine was isolated from the mixed population of the activated sludge unit which was being used for treating complex effluents, the strain was characterized. Aerobic degradation of pyridine was studied with the isolated strain and the growth parameters were evaluated. Pyridine degradation was further conformed by chromatography (HPLC) analysis. The process parameters like biomass growth and dissolved oxygen consumption were monitored during pyridine degradation. In order to conform with the plasmid capability to degrade pyridine, the requisite plasmid was isolated and transferred to DH 5alpha Escherichia coli. The subsequent biodegradation studies revealed the ability of the transformed plasmid capability to degrade the pyridine.     

Degradation of Poly(3-hydroxybutyrate) and Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) by Some Soil Aspergillus spp.

Systematic screening of 45 soil fungi for degradation polyhydroxyalkanoic acids (PHAs) has led to the selection of 6 potent Aspergillus isolates belonging to A. flavus, A. oryzae, A. parasiticus, and A. racemosus. Degradation of PHAs as determined by tube assay method revealed that these Aspergillus spp. were more efficient in degrading poly(3-hydroxybutyrate) [P(3HB)] compared to copolymer of 3-hydroxybutyric acid and 3-hydroxyvaleric acid (P3HB-co-16% 3HV). Moreover, the extent of degradation in mineral base medium was much better than those in complex organic medium. For all the Aspergillus spp. tested, maximum degradation was recorded at a temperature of 37°C with significant inhibition of growth. The optimum pH range for degradation was 6.5–7.0 with degradation being maximum at pH 6.8. The extent of polymer degradation increased with increase in substrate concentration, the optimum concentration for most of the cultures being 0.4% and 0.2% (w/v) for P(3HB) and P(3HB-co-16%3HV) respectively. Supplementation of the degradation medium with additional carbon sources exerted significant inhibitory effect on both P(3HB) and P(3HB-co-16%3HV) degradation.     

A systematic approach to in situ bioremediation in groundwater

In situ bioremediation (ISB) melds an understanding of microbiology, chemistry, hydrogeology, and engineering into a strategy for planned and controlled microbial degradation of specific contaminants. ISB creates subsurface environmental conditions, typically through reduction oxidation manipulation, which induce the degradation of contaminants via microbial catalyzed biochemical reactions. In turn, the microbes produce enzymes that are utilized to derive energy and that are instrumental in the degradation of target chemicals. To accomplish this chain of events, the type of microorganisms, contaminant, and the geological conditions at the site must be considered. Since in situ conditions are manipulated by engineered means, the most important consideration is the ability to transmit and mix liquids in the subsurface. The Interstate Technology Regulatory Council (ITRC)–ISB Team has recently completed a guidance document that describes a systematic approach to ISB in groundwater. ITRC is a state‐led coalition of more than 40 states working together with industry and stakeholders to achieve regulatory acceptance of environmental technologies. © 2003 Wiley Periodicals, Inc.     

Characterization of post-consumer polyolefin wastes by hyperspectral imaging for quality control in recycling processes

In this paper new analytical inspection strategies, based on hyperspectral imaging (HSI) in the VIS–NIR and NIR wavelength ranges (400–1000 and 1000–1700 nm, respectively), have been investigated and set up in order to define quality control logics that could be applied at industrial plant level for polyolefins recycling. The research was developed inside the European FP7 Project W2Plastics “Magnetic Sorting and Ultrasound Sensor Technologies for Production of High Purity Secondary Polyolefins from Waste”. The main aim of the project is the separation of pure polyethylene and polypropylene adopting an innovative process, the magnetic density separation (MDS). Spectra of plastic particles and contaminants resulting from post-consumer complex wastes and of virgin polyolefins have been acquired by HSI and by Raman spectroscopy. The classification results obtained applying principal component analysis (PCA) on HSI data have been compared with those obtained by Raman spectroscopy, in order to validate the proposed innovative methodology. Results showed that HSI sensing techniques allow to identify both polyolefins and contaminants. Results also demonstrated that HSI has a great potentiality as a tool for quality control of feed (identification of contaminants in the plastic waste) and of the two different pure polypropylene and polyethylene flow streams resulting from the MDS-based recycling process.     

A multiple source approach to acute human health risk assessments

The US Army Center for Health Promotion and Preventive Medicine (USACHPPM) has developed a three-tiered approach to perform an acute noncarcinogenic health risk assessment to comply with requirements contained in USEPA’s ‘Addendum to the Methodology for Assessing Health Risks Associated with Indirect Exposure to Combustor Emissions' (USEPA, Draft strategy for combustion of hazardous waste, May 1993). The addendum document drafted in November 1993 suggests evaluation of short-term emissions and exposures, but it does not provide necessary guidance or methodology. This evaluation becomes extremely complex when several sources contribute to the overall concentration of contaminants in the air. Because each source has a different emission rate, location, and dispersion profile, the compound-specific maximum concentrations are rarely located at the same receptor location, as determined by using the Industrial Source Complex Short Term (ISCST3) dispersion model. Furthermore, evaluation of hazard quotients at various receptor locations from a large number of contaminants from multiple sources is an extremely complex and tedious process. This paper will detail a three-tiered approach which was developed to perform the acute risk assessment, quantify possible advantages and disadvantages associated with each tier, and demonstrate the effects of contributing factors, such as distance, emission rate variability, population/exposure scenarios, and compound speciation. In order to accomplish this task, a sample facility with four different combustion sources was modeled and processed according to the three-tiered approach.     

Advances in photocatalytic remediation technology

The cost of remediation at hazardous waste sites is estimated at billions of dollars annually. It is imperative that more cost‐effective remediation technologies be developed, particularly to address the more complex megasites. Chlorinated hydrocarbons represent the major contaminants at many such sites. It has long been recognized that chlorinated hydrocarbons can be destroyed by photocatalytic oxidation. Traditional photocatalysts, however, have often shown inadequate destruction activity, a loss of activity over time, and poor selectivity, thereby producing substantial amounts of phosgene and chloroform by‐products. This article presents results obtained using novel photocatalyst compositions. The results demonstrate the ability to achieve high photocatalytic destruction activity for chlorinated hydrocarbons with full retention of activity over extended time periods and with complete elimination of phosgene and chloroform by‐products. © 2006 Wiley Periodicals, Inc.     

Processability and Biodegradability Evaluation of Composites from Poly(butylene succinate) (PBS) Bioplastic and Biofuel Co-products from Ontario

This study investigates the processability and biodegradability of composite bioplastic materials. Biocomposites were processed using twin-screw compounding of the bioplastic poly(butylene succinate) (PBS) with bio-based fillers derived from co-products of biofuel production. An extensive biodegradability evaluation was conducted on each biocomposite material, as well as the base materials, using respirometric testing to analyze the conversion of organic carbon into carbon dioxide. This evaluation revealed that the presence of meal-based fillers in the biocomposites increased the rate of biodegradation of the matrix polymer, degrading at a faster pace than both the pure PBS polymer and the switchgrass (SG) composite. This degradation was further confirmed using FT-IR and thermal analysis of the material structure before and after biodegradation. The increased biodegradation rate is attributed to the high concentration of proteins in the meal-based composites, which enhanced the hydrolytic biodegradation of the material and facilitated micro-organism growth. The SG-based composite degraded slower than the pure polymer due to its lignin content, which degrades via a different mechanism than the polymer, and slowed the biodegradation process.     

Lignin/Poly(ε-Caprolactone) Blends with Tuneable Mechanical Properties Prepared by High Energy Ball-Milling

Polymer blends between lignin, a natural, widely available, no-cost material, and Poly(ε-caprolactone) (PCL), a biodegradable polymer, have been prepared using the ‘clean’, friendly to the environment, technique of the High Energy Ball Milling (HEBM). Two kinds of lignin have been used, Straw lignin, obtained through the Steam Explosion process (SE lignin), and/or Lignosulphonated one (LS lignin). The tensile mechanical tests have shown that, at certain specific compositions, the blends, in particular those with both SE and LS lignin, have good mechanical properties. In particular, by varying the blend composition it is possible to obtain materials with tuneable properties, therefore useful for different applications. Dynamic-Mechanical-Thermal Analysis (DMTA) reveals substantial immiscibility of the blends. Experiments of UV irradiation show that lignin acts as an UV stabilizer for PCL. The effect is higher with SE lignin, likely due to its low molecular weight, which allows the short lignin chains to diffuse more easily within the amorphous regions of PCL.     

Microbial Enzymes Involved in Polyurethane Biodegradation: A Review

Plastics are present in a lot of aspects of everyday life. They are very versatile and resistant to microbial attack. Polyurethanes are used in several industries and are divided in polyester and polyether polyurethanes and there are different types among them. Despite their microbial resistance, they are susceptible to the attack of fungi and bacteria but the mechanism to elucidate its biodegradation are unknown. There are reports from bacteria and fungi that are capable of degrading polyurethane but the studies about the enzymes that attack the plastic are focused on bacterial enzymes only. The enzymes reported are of type esterase and protease mainly since these enzymes are very unspecific and can recognize some regions in the polyurethane molecule and hydrolyze it. Fungal enzymes have been studied prior the 1990s decade but recently, some authors report the use of filamentous fungi to degrade polyurethane and also report some characteristics of the enzymes involved in it. This review approaches polyurethane biodegradation by focusing on the enzymes reported to date.     

Practical Perspectives of 1,4‐Dioxane Investigation and Remediation

1,4‐Dioxane (dioxane) is a contaminant of emerging concern that is classified by the U.S. Environmental Protection Agency as a likely human carcinogen. Dioxane has been used as a minor or major ingredient in many applications, and is also generated as an unwanted by‐product of industrial processes associated with the manufacturing of polyethylene, nonionic surfactants, and many consumer products (cosmetics, laundry detergents, shampoos, etc.). Dioxane is also a known stabilizer of chlorinated solvents, particularly 1,1,1‐trichloroethane, and has been commonly found comingled with chlorinated solvent plumes. Dioxane plumes at chlorinated solvent sites can complicate site closure strategies, which to date have not typically focused on dioxane. Aggressive treatment technologies have greatly advanced and are clearly capable of achieving lower parts per billion cleanup criteria using ex situ advanced oxidation processes and sorption media. In situ chemical oxidation has also been demonstrated to effectively remediate dioxane and chlorinated solvents. Other in situ remedies, such as enhanced bioremediation, phytoremediation, and monitored natural attenuation, have been studied; however, their ability to achieve cleanup levels is still somewhat questionable and is limited by co‐occurring contaminants. This article summarizes and provides practical perspectives on dioxane analysis, plume stability relative to other contaminants, and the development of investigation tools and treatment technologies.