No description available.

No description available.

Bioremediation of chlorinated aliphatic hydrocarbon (CAH) compounds commonly found at contaminated sites has been an area of focus in recent years. The cometabolic transformation of CAH compounds is important at sites where the redox condition does not favor natural attenuation or populations of indigenous microorganisms are relatively low. At sites where the ground-water system is aerobic, monitored natural attenuation strategies will not meet remediation objectives, or both, enhanced bioremediation via cometabolism is an option. Models are needed to simulate cometabolism in an effort to improve performance and design. The SEAM3D Cometabolism Package was designed to address this need. The objective of this report is to model field data to determine the ability of SEAM3D to simulate the performance of cometabolism. A ground-water flow and transport model was designed based on reported parameters used in the field experiments at Moffett Field. Electron donor and acceptor breakthrough curves were also simulated in an effort to calibrate the model. Several data sets describing the cometabolism of CAHs were used in the cometabolism modeling for calibration to field data. The cometabolism modeling showed areas of best fit calibration with modification to the model parameters reported for the pilot tests at Moffett Field. The overall performance of the SEAM3D Cometabolism Package described in this report establishes validation of the model using field experiment results from the literature. Additional model validation is recommended for other contaminants. / Master of Science

No description available.

The objective of this research was to evaluate the long-term performance of enhanced anaerobic bioremediation (EAB) at chlorinated solvent sites and the occurrence of sustained treatment following EAB. A database of groundwater concentration versus time records was compiled for 25 sites with at least three years of post-treatment data. The median post-treatment monitoring period for these sites was 5.2 years, with a maximum of 11.7 years. Long-term performance was evaluated based on concentration changes from before treatment to the final year of post-treatment monitoring. Results indicate that the median concentration reduction for all 25 sites was approximately 80%, just under 1 order of magnitude. Sustained treatment, where concentrations remain suppressed after ceasing active treatment, was evaluated using a lines-of-evidence approach including analysis of rebound, statistical concentration trends after treatment, and decay rates from before and after treatment. Results indicate that sustained treatment is occurring at a majority of the sites.

No description available.

<p>Chlorinated solvents are common contaminants in soil and water. Under anaerobic conditions microbes are capable of transforming chlorinated solvents into ethylene which would result in a remediation of the contaminated area. In order to use natural attenuation as a remediation method evidence of continuous degradation is required. Furthermore, the degradation must occur at a sufficient rate and continuous monitoring of the site is needed until the demanded levels are achieved. A field study was performed on the basis of data from a dry-cleaning facility contaminated mainly by perchloroethylene. The purpose of the study was to define the existing situation regarding distribution and transformation of contaminant in order to evaluate the possibilities of using natural attenuation as a method of remediation. Degradation of perchloroethylene proceeds through successive removal of chlorine, with the formation of trichloroethylene, dichloroethylene, vinyl chloride and ethylene. There exists evidence of degradation as far as vinyl chloride on the site but whether transformation continues to ethylene is not established. The computer model Biochlor was used to simulate distribution and degradation of the contaminants. The site possesses a complex hydrogeology and the existing data are not sufficient to distinguish the effect of degradation from other factors such as spreading of contaminant between different layers of soil. Since degradation failed to be quantified, natural attenuation can not be recommended as a safe remediation method at the considered site without further investigations.</p> / <p>Klorerade lösningsmedel är vanligt förekommande föroreningar i mark och vatten. Under anaeroba förhållanden kan mikrober omvandla klorerade kolväten till eten vilket leder till rening av det förorenade området. För att kunna använda denna naturliga nedbrytning som saneringsmetod krävs bevis för att nedbrytning fortskrider i tillräcklig utsträckning för att rena området och därefter krävs kontinuerlig provtagning till dess målen för saneringen har uppnåtts. En fallstudie utfördes utifrån data från en kemtvättsfastighet förorenad av i första hand perkloreten. Syftet var att kartlägga föroreningssituationen med avseende på spridning och nedbrytning av de klorerade föreningarna för att undersöka om naturlig nedbrytning var en möjlig framtida saneringsmetod. Nedbrytning av perkloreten sker stegvis genom att klor avspjälkas, under bildande av produkterna trikloreten, dikloreten, vinylklorid och etengas. Nedbrytning av förorening har konstaterats ske på fastigheten fram till vinylklorid men huruvida nedbrytning avstannat där eller fullföljts till etengas är ej klarlagt. Datormodellen Biochlor användes för att simulera spridning och nedbrytning av utsläppet. Fältplatsen har en komplex hydrogeologi och befintliga fältdata var inte tillräckliga för att särskilja nedbrytningens effekt från faktorer såsom spridning av förorening mellan olika jordlager. Eftersom nedbrytningen inte kunde kvantifieras kan naturlig nedbrytning inte rekommenderas som säker saneringsmetod på denna fältplats utan kompletterande analyser.</p>

No description available.

Doctor of Philosophy / Water quality guidelines (WQGs) present concentrations of contaminants that are designed to be protective of aquatic ecosystems. In Australia, guidance for assessment of water quality is provided by the ANZECC and ARMCANZ (2000) Guidelines for Fresh and Marine Water Quality. WQGs are generally provided for individual contaminants, not complex mixtures of chemicals, where interaction between contaminants may occur. Complex mixtures of contaminants are however, more commonly found in the environment than singular chemicals. The likelihood and consequences of adverse effects occurring in aquatic ecosystems resulting from contaminants are generally assessed using an ecological risk assessment (ERA) framework. Ecological risk assessment is often a tiered approach, whereby risks identified in early stages, using conservative assumptions, prompt further detailed and more realistic assessment in higher tiers. The objectives of this study were: to assess and investigate the toxicity of the mixture of volatile chlorinated hydrocarbons (VCHs) in groundwater to indigenous marine organisms; to present a ‘best practice’ ecological risk assessment of the discharge of contaminated groundwater to an estuarine embayment and to develop techniques to quantify the environmental risk; and to evaluate the existing ANZECC and ARMCANZ (2000) WQGs for VCHs and to derive new WQGs, where appropriate. Previous investigations at a chemical manufacturing facility in Botany, Sydney, identified several plumes of groundwater contamination with VCHs. Contaminated groundwater containing a complex mixture of VCHs was identified as discharging, via a series of stormwater drains, to surface water in nearby Penrhyn Estuary, an adjacent small intertidal embayment on the northern margin of Botany Bay. A screening level ecological hazard assessment was undertaken using the hazard quotient (HQ) approach, whereby contaminant concentrations measured in the environment were screened against published trigger values (TVs) presented in ANZECC and ARMCANZ (2000). Existing TVs were available for 9 of the 14 VCHs present in surface water in the estuary and new TVs were derived for the remaining 5 VCHs. A greater hazard was identified in the estuary at low tide than high tide or when VCH concentrations from both high and low tides were assessed together. A greater hazard was also identified in the estuary when the toxicity of the mixture was assessed, rather than the toxicity of individual contaminants. The screening level hazard assessment also identified several limitations, including: the low reliability of the TVs for VCHs provided in ANZECC and ARMCANZ (2000); the limited applicability of the TVs to a complex mixture of 14 potentially interacting contaminants; the use of deterministic measures for each of the exposure and toxicity profiles in the HQ method and the associated lack of elements of probability to assess ‘risk’. Subsequent studies were undertaken to address these identified shortcomings of the screening level hazard assessment as described in the following chapters. A toxicity testing methodology was adapted and evaluated for suitability in preventing loss of VCHs from test solutions and also for testing with 6 indigenous marine organisms, including: oyster (Saccostrea commercialis) and sea urchin larvae (Heliocidaris tuberculata); a benthic alga (Nitzschia closterium); an amphipod (Allorchestes compressa); a larval fish (Macquaria novemaculeata); and a polychaete worm (Diopatra dentata). The study evaluated possible VCH loss from 44 mL vials for small organisms (H.tuberculata, S.commercialis and N.closterium) and 1 L jars for larger organisms (M.novemaculeata, A.compressa and D.dentata). Vials were effective in preventing loss of VCHs, however, an average 46% of VCHs were lost from jars, attributable to the headspace provided in the vessels. Test jars were deemed suitable for use with the organisms as test conditions, i.e. dissolved oxygen content and pH, were maintained, however, variability in test organism survival was identified, with some control tests failing to meet all acceptance criteria. Direct toxicity assessment (DTA) of groundwater contaminated with VCHs was undertaken using 5 indigenous marine organisms and site-specific species sensitivity distributions (SSDs) and TVs were derived for the complex mixture of VCHs for application to surface water in Penrhyn Estuary. Test organisms included A.compressa, H.tuberculata, S.commercialis, D.dentata and N.closterium. The SSD was derived using NOEC data in accordance with procedures presented in ANZECC and ARMCANZ (2000) for deriving WQGs. The site-specific SSD adopted was a log-normal distribution, using an acute to chronic ratio (ACR) of 5, with a 95% TV of 838 μg/L total VCHs. A number of additional scenarios were undertaken to evaluate the effect of including different ACRs (i.e. 5 or 10), inclusion of larval development tests as either acute or chronic tests and choice of SSD distribution (i.e. log-normal, Burr Type III and Pareto). TVs for the scenarios modelled varied from 67 μg/L to 954 μg/L total VCHs. A site-specific, quantitative ERA was undertaken of the surface water contaminated with VCHs in Penrhyn Estuary. The risk assessment included probabilistic elements for toxicity (i.e. the site-specific SSD) and exposure (i.e. a cumulative distribution function of monitoring data for VCHs in surface waters in the estuary). The joint probability curve (JPC) methodology was used to derive quantitative estimates of ecological risk (δ) and the type of exposure in the source areas in surface water drains entering the estuary, i.e. Springvale and Floodvale Drains, Springvale and Floodvale Tributaries and the Inner and Outer Estuary. The risk of possible adverse effects and likely adverse effects were each assessed using SSDs derived from NOEC and EC50 data, respectively. Estimates of risk (δ) of possible adverse effects (i.e. based on NOEC data) varied from a maximum of 85% in the Springvale Drain source area to <1% in the outer estuary and estimates of likely adverse effects (i.e. based on EC50 data) varied from 78% to 0%. The ERA represents a ‘best practice’ ecological risk assessment of contamination of an estuary using site-specific probabilistic elements for toxicity and exposure assessments. The VCHs identified in surface water in Penrhyn Estuary are additive in toxicity and act under the narcotic pathway, inhibiting cellular processes through interference with membrane integrity. Lethal toxicity to 50% of organisms (i.e. LC50) is typically reported at the internal lethal concentration (ILC) or critical body residue (CBR) of ~2.5 mmol/kg wet weight or within the range of 1 to 10 mmol/kg wet weight. To evaluate the sensitivity of the test organisms to VCHs and to determine if toxicity in the DTA was due to VCHs, the internal residue for 6 test organisms was calculated for the mixture of VCHs in groundwater and toxicity testing with seawater spiked individually 2 VCHs, chloroform and 1,2-dichloroethane. Calculated residues (at LC50/EC50) were typically between 1 and 10 mmol/kg, with the exception of the algal and sea urchin toxicity tests, which were considerably lower than the expected minimum. Mean internal residues for the groundwater, chloroform and 1,2-dichloroethane were 0.88 mmol/kg, 2.84 mmol/kg and 2.32 mmol/kg, respectively, i.e. close to the predicted value of ~2.5 mmol/kg, indicating that the organisms were suitably sensitive to VCHs. There was no significant difference (P>0.05) between the mean residues of each of the three treatments and the study concluded that the additive toxicity of the VCHs in groundwater was sufficient to account for the observed toxicity (i.e. VCHs caused the toxicity in the DTA undertaken). Evaluation of the existing low reliability ANZECC and ARMCANZ (2000) TVs for chloroform and 1,2-dichloroethane was undertaken to determine if these guidelines were protective of indigenous marine organisms. NOECs, derived from toxicity testing of 1,2- dichloroethane and chloroform with 6 indigenous marine organisms, were screened against the existing low reliability TVs. The TVs for 1,2-dichloroethane and chloroform were protective of 4 of the 6 species tested (A.compressa, D.dentata, S.commercialis and M.novemaculeata), however, the TVs were not protective of the alga (N.closterium) or the sea urchin larvae (H.tuberculata). As the existing TVs were not considered to be adequately protective, SSDs were derived using the NOEC data generated from the testing in accordance with procedures outlined in ANZECC and ARMCANZ (2000). Moderate reliability TVs of 3 μg/L and 165 μg/L were derived for chloroform and 1,2- dichloroethane, respectively, i.e. considerably lower than the existing TVs of 770 μg/L and 1900 μg/L. Differences between the existing and newly derived TVs were considered to result from the sensitive endpoints selected (i.e. growth and larval development rather than survival) and from variability inherent when deriving SSDs using a small number of test species. Ongoing groundwater monitoring indicated that the plumes of VCHs in groundwater, identified in the 1990s, were continuing to migrate towards Botany Bay. Discharge of these groundwater plumes into Botany Bay would result in significant increases in the concentrations of VCHs in the receiving environment and would likely lead to significant environmental impacts. In 2006, a groundwater remediation system was commissioned to prevent the discharge of groundwater containing VCHs into Penrhyn Estuary and Botany Bay. The success of the project had only been measured according to chemical and engineering objectives. Assessment of changes in ecological risk is vital to the success of ERA and central to the ERA management framework. Whereas monitoring of chemical concentrations provides qualitative information that risk should decrease, it cannot quantify the reduction in ecological risk. To assess the ecological risk following implementation of the groundwater treatment system, the risk assessment was revised using surface water monitoring data collected during 2007 and 2008. The ERA indicated that, following remediation of the groundwater, ecological risk in Penrhyn Estuary reduced from a maximum of 35% prior to remediation, to a maximum of only 1.3% after remediation. Using the same methodology applied in the initial risk assessment, the success of the groundwater remediation was measured in terms of ecological risk, rather than engineering or chemical measures of success. Prior to the present investigation, existing techniques for assessing ecological risk of VCH contamination in aquatic ecosystems were inadequate to characterise ecological risk. The current study demonstrated that through monitoring of surface water at the site and DTA using indigenous marine organisms, ecological risk can be assessed using site-specific, quantitative techniques for a complex mixture of VCHs in groundwater. The present investigation also identified that existing ANZECC and ARMCANZ (2000) low reliability TVs were less protective of indigenous test organisms than previously thought and therefore, new TVs were derived in the current work. The present study showed that revision of the risk assessment as conditions change is crucial to the success of the ecological risk management framework.

The findings of this study demonstrate that Dehalococcoides species are intimately involved in complete reductive detoxification of chlorinated ethenes and are widely distributed in anoxic sediments and aquifers, including non-contaminated (pristine) environments. Careful examination of enrichment culture dechlorination kinetics, 16S rRNA gene based analyses, and reductive dehalogenase gene targeted PCR approaches revealed that complete reductive dechlorination is carried out by multiple dechlorinators. Two new dechlorinating species were isolated from contaminated and non-contaminated site materials. The first new isolate, designated strain SZ, was isolated from PCE-to-ethene dechlorinating microcosms established with creek sediment. 16S rRNA gene sequence of the strain SZ indicates that the new isolate is affiliated with the genus Geobacter most closely related to G. thiogenes. Strain SZ is capable of stepwise dechlorination of PCE to cis-DCE, while the closest relatives were not able to dechlorinate PCE or TCE. Dechlorination of PCE or TCE by strain SZ was supported by acetate, hydrogen or pyruvate as electron donor. Chloroethene-dechlorinating populations have been shown to have distinct electron donor requirements. However, none of previously described chlorinated ethene degrading population can use both, acetate and hydrogen, as electron donors. PCE dechlorination by strain SZ uses both acetate and hydrogen as electron donors suggesting that the ability to versatile electron donor utilization may increase the efficiency of bioremediation approaches. Importantly, strain SZ reduced two environmental priority pollutants, PCE and U(VI) concomitantly and detected from both bio-stimulated chloroethene and uranium contaminated sites, strongly suggesting that strain SZ play a important roles in in-situ bioremediation of chloroethene and U(VI) contaminated sites. The second, a new Dehalococcoides species designated strain GT, was isolated from contaminated site materials. Strain GT uses trichloroethene (TCE), cis-DCE, 1,1-dichloroethene (1,1-DCE), and the human carcinogen vinyl chloride (VC) as growth supporting electron acceptors producing products ethene and inorganic chloride. The new isolate shares common traits of Dehalococcoides such as ampicillin resistance, strict hydrogen-dependent metabolism, and a low hydrogen consumption threshold concentration. Culture-dependent and independent, 16S rRNA gene and reductive dehalogenase gene targeted PCR approaches suggested culture purity.