Growth of bacteria in drinking water distribution and storage systems can lead to the deterioration of water quality, violation of water standards, and increased operating costs. Growth or Regrowth results from viable bacteria surviving the disinfection process and utilizing nutrient in the water and biofilm to sustain growth. Factors other than nutrients that influence regrowth include temperature, residence time in mains and storage units, and the efficacy of disinfection. Tests to determine the potential for bacterial regrowth focus on the concentration of nutrients. Not all organic compounds are equally susceptible to microbial decomposition; the fraction that provides energy and carbon for bacterial growth has been called labile dissolved organic carbon, biodegradable organic carbon (BDOC), or Assimilable Organic Carbon (AOC). Easily measured chemical surrogates for AOC are not available now. As alternative to chemical methods, bioassays have been proposed. Assimilable Organic Carbon (AOC) is that portion of the biodegradable organic carbon that can be converted to cell mass and expressed as a carbon concentration by means of a conversion factor. In this study, two organisms, namely Psuedomonas fluorescens strain P17 and Spirillum species NOX were selected for the AOC determination. The growth of the bacteria was determined by periodic colony counts with spread plate technique on LLA (Lab-Lemco nutrient agar) cultivation medium until the growth reached maximum (maximum colony count, Nmax). Results showed that AOC follows a trend based on the climatic and seasonal changes (local climate) with peaks in summer and low during winter season and vice versa in term of AOC removing capability. In addition to confirm AOC removal rate in biofiltration bed was evaluated with a test column containing the same filling materials, Granular Activated Carbon (GAC). Long term test showed that GAC would last for forty weeks without any special treatment. Other result showed that biofiltration bed has a better removal efficiency rate 72% (average based on four year), than the test column 49% since it experience frequent back-washing, thus maintaining a healthy removal rate. In the test column change in total organic carbon was quite abnormal. AOC yearly distribution was also studied and differentiated into four stages. AOC removal of each stage was 48%, 70%, 83% and 77%. Total organic carbon concentration was much higher in the effluent 384 than influent 334 £gg C/L; later methionine was found in water sample (effluent) which strongly suggests that the indigenous microbes had been reducing organic material such as cystein to methionine thus increasing the organic carbon content of the effluent. The microbial growths inside the GAC test column is entirely based on the long term feed of water at the treatment plant. Several other parameters such as Scanning Electron Microscope (SEM), Excitation Emissions Fluorescence Matrix (EEFM), Molecular Weight and Amino acids detection were selected and coupled with the AOC to shed light on the working mechanisms of both GAC as filtration material and characteristics of indigenous microbes towards the removal of organic contaminants and changes they can bring about to the quality of clear water.

Thesis (Ph. D.)--Oregon State University, 2010. / Printout. Includes bibliographical references (leaves 190-208). Also available on the World Wide Web.

Thesis (Ph.D.)--York University, 2007. Graduate Programme in Chemistry. / Typescript. Includes bibliographical references. Also available on the Internet. MODE OF ACCESS via web browser by entering the following URL: http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:NR39012

Thesis (Ph. D.)--University of Missouri-Columbia, 2000. / Typescript. Vita. Includes bibliographical references (leaves 112-120). Also available on the Internet.

Thesis (Ph. D.)--University of Missouri-Columbia, 2000. / Typescript. Vita. Includes bibliographical references (leaves 112-120). Also available on the Internet.

Title from PDF of title page (University of Missouri--Columbia, viewed on Feb 18, 2010). The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file. Thesis advisor: Dr. Jeffre Firman. Includes bibliographical references.

Thesis (M.S.)--Mississippi State University. Department of Chemistry. / Title from title screen. Includes bibliographical references.

Shell organic matrix proteins in fossils are valuable geochemical archives for studying ancient environments and food webs. Compound-specific studies of stable carbon isotope ratios offer particularly good resolution of trophic level of consumers and the identities of primary producers and can be used to detect diagenetic alteration of isotopic ratios. To interpret compound specific isotope data, however, controlled diet studies in the laboratory are needed to reveal trophic enrichment patterns of 13C in tissues and shell organic matter. This study examines the relationship between d 13C of 11 amino acids in diet, soft tissues, and shell organic matter in laboratory-cultured Strombus alatus, an herbivorous marine gastropod. The d 13C values of amino acids in this animal's foot and mantle tissues are consistently enriched in 13C relative to the diet. Phenylalanine (+1.8 ppm) and alanine (+3.8 ppm) showed the least fractionation between diet and tissues, while aspartic acid (+10.7 ppm) and glutamic acid (+14.6 ppm) showed the greatest enrichment. On average, nonessential amino acids exhibited greater enrichment than did essential amino acids (+7.1 ppm vs. + 4.1 ppm). Shell organic matter amino acids showed a very similar pattern, with aspartic and glutamic acids again showing the greatest enrichment (+7.2 ppm and +11.1 ppm respectively). Nonessential amino acids in shell (+4.9 ppm) were also more enriched than the essential amino acids (+3.5 ppm). Overall, the carbon isotopic compositions of amino acids in shell organic matrix appear to parallel those in animal tissue, validating the utility of employing this material as a surrogate for animal tissue in fossil samples. Interpreting trophic position information in consumers is difficult, however, as the variation in the magnitude of trophic enrichments for glutamic and aspartic acids between species, tissue types and diet is still poorly understood. As phenylalanine has the most consistent diet-consumer enrichments, the most suitable application for d 13C isotope analysis at this time is the reconstruction of base food sources.

published_or_final_version / Zoology / Master / Master of Philosophy

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