One advantage of Integrated Multi-Trophic Aquaculture (IMTA) is the potential for bioremediation by organic-extractive organisms. In British Columbia, a number of marine invertebrate species are being considered for use in open-water IMTA with sablefish (Anoplopoma fimbria). These include both filter-feeding bivalves (e.g. cockles, mussels, oysters, scallops) which would consume the finer suspended particulates from the finfish culture component and deposit/detrital feeders (e.g. sea cucumbers, sea urchins, prawns) which would feed on the heavier-settleable solids. The following candidate species were tested for their ability to consume sablefish faeces and uneaten sablefish feed in laboratory feeding trials: green sea urchin (Strongylocentrotus droebachiensis), basket cockle (Clinocardium nuttallii), blue mussel (Mytilus edulis), spot prawn (Pandalus platyceros), and California sea cucumber (Parastichopus californicus). Whether they can remove organic material from aquaculture wastes was tested by measuring ingestion rate or clearance rate and absorption efficiency when they were fed a diet of sablefish waste, relative to those fed a natural control diet. Egestion rates in the candidate species were quantified to estimate the potential amount of waste that may be lost from the organic-extractive component. Biophysical properties including shape, size, and settling velocity were measured in faecal pellets egested by the candidate species to provide input data for models to assess dispersal of faeces from IMTA sites. Results from the laboratory feeding trials demonstrate that all candidate species are capable of consuming wastes from sablefish aquaculture and absorbing the organic material. The relative merits and drawbacks of each candidate species are discussed with respect to the results and within the broader context of IMTA. The general conclusion is that, in order to achieve efficient removal of organic material and successful bioremediation, deposit feeders should be included in the organic-extractive component, whether alone or in conjunction with suspension feeders. / Graduate

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This study aims to determine the factors that affect the implementation of marine pollution policy, especially with regard to regulation of the hazardous substances which contaminate the marine environment- The purpose is to identify weaknesses in the current regulatory regime and to propose improvements. The study also aims to develop a new strategic framework for the implementation of the recent international policy commitments, which call for the complete cessation of discharges of hazardous substances into the marine environment by the year 2020. Furthermore, the study seeks to provide evidence to support or challenge current theories relating to regulation and policy implementation. Examination was made of the attitudes of environmental managers from the UK chemical industry and inspectors from the environmental agencies towards the regulatory system. These are the key personnel who operate at the regulatory interface where the policy outcome is determined. The methodology combined both qualitative and quantitative techniques. Structured interviews helped define the issues for subsequent investigation using a questionnaire survey which was sent to over 700 key personnel. Focus groups were then used to explain the survey findings and develop solutions to key regulatory problems. Statistical analysis of the survey response data revealed similarities and significant differences between the views of industry and the regulator on the effectiveness of the current Integrated Pollution Control regime. The strength of the system was perceived as its practical and pragmatic approach, coupled with a convenient and familiar bureaucracy. The weaknesses identified related to the derivation and enforcement of standards. The Environmental Quality Standards system, which underpins the regime, was acknowledged to be flawed by both operators and regulators who agreed it should be improved by the expansion in the number of priority listed chemicals, the introduction of sediment Environmental Quality Standards and Direct Toxicity Assessment of effluents. Focus groups supported the expansion of the system, but recognised that it would create a regime that was both complex and impractical. The findings were used to construct a revised model of the existing regime. Multivariate analysis of the industry response data identified 3 cluster types and significant differences were revealed between their knowledge of policy developments, their implications and the need for changes to the current system of hazardous chemical control. Operators and regulators acknowledged the existence of the mutual interdependency which has created and maintained a tight policy network (community) at the regulatory interface. Further evidence to support the existence of this community and of regulatory capture, was provided by the study data. Focus group discussions also identified the requirement for a more fundamental reappraisal of the regulatory system in order to deliver the OSPAR strategy. A new regulatory model, which incorporates process and product substitution, is proposed as a strategic framework to ensure that future policy commitments are implemented. This approach may lead to the opening up of the current tight policy network with resultant benefits for policy implementation and reduced regulatory capture. The new model could be applied by other countries within the OSPAR region and in other regions of the world, in order to improve environmental protection.

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Activated carbons are used widely for the adsorption of environmentally unfriendly species from both liquid and gas phases, the separation of gases and adsorption of species from aqueous solution. Examples of the processes are the adsorption of Au(CN)2 and Ag(CN)2 from aqueous solution for the recovery of precious metals, the treatment of waste water containing organic chemicals and toxic metal species and the preparation of metal catalysts supported on carbon. This investigation has involved the study of the influence of porous structure and surface functional groups on the adsorption of both anionic and cationic metal species in order to understand the mechanism of adsorption of these species on active carbon from aqueous solution. Various types of oxygen functional groups were introduced onto the surface of coconut shell derived activated carbon through oxidation using nitric acid. Fourier transform infrared spectroscopy (FTIR), temperature programmed desorption (TPD) and selective neutralisation were used to characterise the surface oxygen functional groups. The oxidised carbons were also heat treated to provide a suite of carbons where the oxygen functional groups of various thermal stability were varied progressively. It was found that acidic oxygen functional groups mainly as carboxylic acid groups were incorporated into activated carbon by HNO3 oxidation. The phenol and quinone groups were also introduced by the oxidation process while the lactone groups were formed during heat treatment. The oxygen functional groups had a range of thermal stabilities with carboxylic acid groups being the least stable. A coconut shell derived active carbon was treated with ammonia and nitric acid followed by ammonia to incorporate nitrogen functional groups into the carbon. Active carbon with high nitrogen content was also prepared from nitrogen-rich precursor polyacrylonitrile (PAN). X-ray absorption near edge structure spectroscopy (XANES) and FTIR were used to investigate the structures of the nitrogen functional groups in carbons. The possible nitrogen functional groups present on carbon surface were pyridinic, pyrrolic (or indolic), pyridonic and aromatic amine-like structures. The adsorption characteristics of gold and silver cyanide anionic species on a suite of active carbons derived from coconut shell, polyacrylonitrile and chemical modification of the coconut shell carbon were investigated. The gold and silver cyanide adsorption capacities for coconut shell derived carbons correlate with total pore volume. Nitric acid oxidation treatment of the carbon was detrimental to gold adsorption in spite of the incorporation of oxygen content of carbon. The influence of nitrogen functional groups in the carbon structure on gold and silver adsorption was investigated using carbons derived from polyacrylonitrile. The addition of ethanol and butanol to the solution had an adverse effect on gold adsorption. Adsorption of silver cyanide ionic species on the active carbon was suppressed in the presence of excess free cyanide ions in solution whereas gold cyanide adsorption was not greatly affected at room temperature. The adsorption of gold cyanide was suppressed by the excess free cyanide and sodium sulphide at 70 °C. The adsorption of cadmium ions was enhanced dramatically by oxidation of the carbon. The ratio of released proton to adsorbed cadmium on oxidised carbon was approximately 2 indicating cation exchange was involved in the adsorption process. Na+ exchange studies with the oxidised carbon gave a similar ratio. After heat treatment of the oxidised carbons to remove oxygen functional groups, the ratio of H+/Cd2+ decreased significantly as well as the adsorption capacity. Both reversible and irreversible adsorption were involved in the process of cadmium adsorption with reversible adsorption having higher enthalpy. The irreversible adsorption resulted from cation exchange with carboxylic acid groups whereas the reversible adsorption probably involved physisorption of the partially hydrated cadmium ion. The nitrogen functional groups may act as ligands which can coordinate with transition metal cations. The adsorption of transition metal cations such as Cd 2+, Ni2+ and Cu2+ on active carbon was appreciably increased by the nitrogen functional groups present on carbon surface whereas ammonia treatment of the carbon showed little effect on the adsorption of alkali earth metal cation Cat+. There is little difference in the adsorption capacities of cadmium ions on coconut shell derived carbon at pH 4.1 and pH 7 whereas the adsorption of cadmium ions was significantly enhanced with increasing pH for the carbons with high nitrogen content. The nitrogen rich carbons show selectivity towards various transition metal cations reflected by adsorbing more Cu 2+ than Cd2+. This is consistent with the fact that the coordination compound of Cu 2+ with pyridine has higher stability constant than that of cadmium.

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Biopolymers are polymers produced by certain microorganisms, that are readily degradable in the environment. These biodegradable plastics have the potential to be used as substitutes for conventional petroleum based plastic provided that the production costs can be greatly reduced. The high cost of biopolymer production is due to the cost of substrate which mainly is glucose. / The enzymatic hydrolysis of potato processing wastes was to produce glucose as a least expensive feedstock substrate for the production of biopolymers of polyhydroxybutirate (PHB) from the bacterium Alcaligenes eutrophus was studied. The enzymatic hydrolysis experiments were carried out using $ alpha$-amylase liquefaction enzymes from Aspergillus oryzae and barley-malt, and amyloglucosidase saccharification enzyme from Rhizopus. / The results indicated that the production of glucose from potato starch waste to be used as a substrate to produce biopolymers was both technically and economically feasible. A 10 to 90 ratio of barley-malt to potato starch waste gave the highest conversion of starch to glucose of 194.30 gL$ sp{-1}$ (96.56%), and the lowest liquefaction enzyme cost ($0.054) to hydrolyze one kg of potato starch waste. { it A. eutrophus /} produced PHB of 5.0 gL$ sp-1$ (76.9 % of biomass) using the glucose substrate generated from the potato starch waste.