Alginates are copolymers of &beta / -D-mannuronic (M) and &alpha / -L-guluronic acids (G). In this study, Azotobacter vinelandii ATCC&reg / 9046 was used to produce alginate in a fermentor. The effect of parameters such as dissolved oxygen tension (DOT), agitation speed, initial concentrations of sucrose and calcium on the properties of alginate were examined. Changes of DOT in the range of 1 and 10 % affected alginate production. The optimum DOT giving high alginate yield (4.51 g/L) and maximum viscosity was observed as 5 % yielding moderate GG-blocks of 55 %. Both high and low agitation levels reduced alginate production, but these conditions increased GG-block alginates as 76 and 87 % at 200 and 700 rpm, respectively. Moderate sucrose and calcium concentrations, 20 g/L and 50 mg/L, respectively were found better since further increase in their concentrations did not lead to a considerable improvement in alginate production and quality. Sodium alginates produced in this work were investigated for maximum heavy metal uptake with a special focus on copper ion and the highest copper uptake was around 1.9 mM Cu2+/g alginate. Findings showed that the block distribution of alginate was not as important as expected for copper removal. Alginate together with calcium ions was used for the removal of turbidity. The amount of GG-block was found to be important in turbidity removal. Alginate having 55 % GG block and 8.9 cP viscosity resulted in a final turbidity lower than 1 NTU at 2 mg/L of alginate with 60 mg/L of calcium ion.

Endocrine disrupters and trace organic contaminants are recently recognized contaminants in wastewaters. Current concept is the multibarier approach where the contaminants are removed from the water cycle both by water and wastewater treatment facilities, as well as natural die-away. In this thesis work LC/MS/MS determination of selected EDC compounds, namely, diltiazem, progesterone, estrone, carbamazepine, benzyl butyl phthalate and acetaminophen, at ultra trace levels, have been carried out by optimizing analytical parameters. In addition, new methods were developed for their analysis in sludge samples at sub ppb levels. Following optimization and method development, occurrence of these contaminants in wastewaters and their removal in two full-scale and two pilot-scale membrane biological reactors (MBRs) was studied. Progesterone, estrone and acetaminophen were completely removed from wastewater by biodegradation. CBZ and diltiazem were not removed at all during the study. There was little effect of flux and sludge retention times on the removal of selected EDCs in these membrane plants. In SBR combined with membrane filtration, 13 different micropollutants, including Fluoxetine (FLX), Ibuprofen (IBP), Naproxen (NPX), Diclofenac (DCF), Carbamazepine (CBZ), Trimethoprim (TMP), Roxithromycin (ROX), Erythromycin (ERY), Sulfamethoxazole (SMX), Diazepam (DZP), Galaxolide (GLX), Tonalide (TON), Celestolide (CEL). CEL, GLX, TON and FLX were removed by adsorption onto the sludge while ROX, ERY, SMX, IBP and NPX were removed by biological degradation. The CBZ, DZP, TMP and DCF were not removed by biodegradation or adsorption. Whereas, following the addition of powdered activated carbon, all these compounds were removed entirely from the wastewater stream by accumulating in sludge.

Thesis (M.A.)--Florida State University, 2004. / Advisor: Dr. Cheryl Ward, Florida State University, College of Arts and Sciences, Department of Anthropology. Title and description from dissertation home page (viewed June 16, 2004). Includes bibliographical references.

Thesis (M.L.A.)--University of Hong Kong, 1999. / Includes special study report entitled: Influence of vegetation on slope stabilization and landscape development on slope. Includes bibliographical references.

published_or_final_version / Botany / Master / Master of Philosophy

The fate and occurrence of Giardia and Cryptosporidium were studied in the marine environment to assess their potential for transmission since their transmission to swimmers in fresh waters has been previously documented. The first part of this study was designed to determine the occurrence of Giardia and Cryptosporidium at bathing beaches within the vicinity of an outfall discharging primary treated sewage into Mamala Bay, Hawaii. Sites were monitored monthly and quarterly for parasites by passing 400 liters of marine water through a spun polyproplyene fiber filter. Giardia and Cryptosporidium were detected in primary treated sewage from the Sand Island sewage treatment plant which discharges into Mamala Bay at concentrations of 2,560 cysts and 216 oocysts/liter, respectively. Ala Wai Canal as well as the bathing beaches within the vicinity of the outfall were also found to contain the parasites. The survival of Giardia in marine water was studied in direct sunlight and the dark in marine waters (33- to 35-ppt salinity), canal water (28-ppt salinity) and in phosphate-buffered saline (8-ppt) at 18 to 28°C. Giardia muris was inactivated by 3-logs in the presence of sunlight in marine and canal waters. In comparison, Giardia survive up to 6 hours in PBS under the same conditions. Overall, it appears that salinity and sunlight quickly inactivate Giardia cysts. Thus, Giardia would pose a threat only if the cysts reach the bathing beaches within a few hours. The last phase of this project was designed to develop a more efficient method of collection of cysts and oocysts from water. Methods for the concentration of enteric viruses, Giardia and Cryptosporidium from water requires the use of two different types of filters. This study compared the efficiency of their concentration from tap water and tertiary treated wastewater with a polypropylene fiber cartridge, and the Filterite electronegative and the 1MDS Virosorb electropositive microporous filters. Results indicated that the overall efficiency was greatest for the Filterite filter for both Giardia and Cryptosporidium (p = 0.000762 and p = 0.067069, respectively); and in addition they are easier and faster to process than the polypropylene-wound parasite filter.

This study measured the actual water consumption of sanitary fixtures installed in restrooms of a university building while most studies have been based on the manufacturer's reported flow rate. Furthermore, this study analyzed the appropriateness of retrofitting with low-consumption water closets and urinals based on the actual water consumption. The purpose of this study is to analyze the cost-effectiveness of water savings from retrofitting water closets and urinals in restrooms of the Langford Architecture building A at Texas A&M University. The researcher directly measured the actual water-volume per flush of as-is, tune-up, low-consumption manual, and low-consumption automatic water closets and urinals. The data collected by these observations was analyzed, and the researcher evaluated the water savings of retrofitting water closets and urinals. Finally, this study provides the actual water-consumption data of sanitary fixtures and proves that retrofitting with low-consumption fixtures can save on water costs. The results will present practical standards to facility managers and other building professionals and will also contribute to determining the feasibility of retrofitting water closets and urinals.

Thesis (M.Tech.: Biotechnology)-Dept. of Biotechnology, Durban Institute Of Technology, 2005 xxiii, 172 p. : ill. ; 30 cm / The provision of safe and sanitary water is a constitutional right and above all, a necessity of life. As a result of the rapid urbanisation and the past policies of apartheid, a large population of South Africa dwell in informal settlements, where there is very little hope of development, as the government does not possess the resources that are necessary for a full-scale sanitation programme. Therefore, on-site treatments have been considered to provide sanitation in these dense peri-urban areas. The anaerobic baffled reactor (ABR) is one such sanitation system. This reactor utilises the phenomenon of anaerobic digestion to degrade substrates. One of the major disadvantages of any anaerobic treatment processes is the extreme sensitivity of the bacterial communities, thus inducing slow recovery rates following toxic shocks. Therefore, an understanding of these microbial consortia is essential to effectively control, operate and optimise the anaerobic reactor. Fluorescence in situ hybridization, 4’,6-diamidino-2-phenylindole (DAPI) staining and DNA sequencing techniques were applied to determine the microbial consortium, as well as their reactions to daily operating conditions. With an understanding of these populations and their responses to perturbations within the system, it is possible to construct an anaerobic system that is successful in its treatment of domestic wastewater. In situ hybridizations were conducted for three operating periods, each characterised by specific flow rates. Results showed Eubacterial population dominance over the Archaeal population throughout both of the operating periods investigated. However, these cells cumulatively consisted of 50% of the total biomass fraction, as determined by DAPI staining. Group-probes utilised revealed a high concentration of fermentative acidogenic bacteria, which lead to a decrease in the pH values. It was noted that the ABR did not separate the acidogenic and methanogenic phases, as expected. Therefore, the decrease in pH further inhibited the proliferation of Archaeal acetoclastic methanogens, which were not present in the second operating period. DNA sequencing results revealed the occurrence of the hydrogenotrophic Methanobacterium and Methanococcus genera and confirmed the presence of Methanosarcina. Sequencing of the bacterial DNA confirmed the presence of the low G+ C Gram Positives (Streptococcus), the high G+C Gram Positives (Propionibacterium) and the sulfate reducing bacteria (Desulfovibrio vulgaris). However, justifications were highly subjective due to a lack of supportive analytical data, such as acetate, volatile fatty acids and methane concentrations. Despite this, findings served to add valuable information, providing details on the specific microbial groups associated with ABR treatment processes.

Thesis (M.Tech.: Biotechnology)-Dept. of Biotechnogy, Durban Institute of Technology, 2005 xvi, 85 leaves : ill. ; 31 cm / Atmospheric nitrogen pollution is on the increase and human activities are directly or indirectly responsible for the generation of the various nitrogen polluting compounds. This can lead to the two major problems of eutrophication and groundwater pollution. Therefore, the removal of nutrients such as nitrogen and phosphorus from wastewater is important. Nitrogen removal from wastewater is achieved by a combination of nitrification and denitrification. Thus, there is a need to identify and characterise heterotrophic denitrifying bacteria involved in denitrification in wastewater treatment systems. The aim of this study, therefore, was to characterise heterotrophic denitrifying bacteria through detailed biochemical and molecular analysis, to facilitate the understanding of their functional role in wastewater treatment systems. Drysdale (2001) isolated heterotrophic denitrifiers to obtain a culture collection of 179 isolates. This culture collection was used to screen for nitrate and nitrite reduction using the colorimetric biochemical nitrate reduction test. The isolates were thereafter Gram stained to assess their gram reaction, cellular and colonial morphology. Based on these results identical isolates were discarded and a culture collection of approximately 129 isolates remained. The genetic diversity of the culture collection was investigated by the analysis of polymerase chain reaction (PCR)-amplified 16S ribosomal DNA (rDNA) fragments on polyacrylamide gels using denaturing gradient gel electrophoresis (DGGE). Thus DNA fragments of the same length but different nucleotide sequences were effectively separated and microbial community profiles of eight predominant isolates were created. Batch experiments were conducted on these eight isolates, the results of which ultimately confirmed their characterisation and placed them into their four functional groups i.e. 3 isolates were incomplete denitrifiers, 2 isolates were true denitrifiers, 2 isolates were sequential denitrifiers and 1 isolate was an exclusive nitrite reducer.

Thesis (M.Tech.: Biotechnology)-Dept. of Biotechnology, Durban Institute of Technology, 2005 xiv, 114 leaves : ill. 30 cm / The activated sludge process is the mostl used biological treatment process. Engineers and microbiologists are constantly seeking ways to improve process efficiency, which can be attributed to the increasing demand for fresh water supplies and proper environmental management. Since the inception of the activated sludge process, bulking and foaming have been major problems affecting its efficiency. Filamentous bacteria have been identified as the primary cause of bulking and foaming. Numerous attempts have been made to resolve this problem. Some of these attempts were effective as interim measures but failed as long term control strategies. The identification of filamentous bacteria and the study of their physiology have been hampered by the unreliability of conventional microbiological techniques. This is largely due to their morphological variations and inconsistent characteristics within different environments. To fully understand their role in promoting bulking and foaming, filamentous bacteria need to be characterized on a molecular level. The aim of this study was, therefore, to identify filamentous bacteria in pure culture with the purpose of validating these findings to the physiological traits of the pure cultures when they were isolated. Fourteen different filamentous cultures were used for this study. The cultures were identified using specific oligonucleotide probes via fluorescent in situ hybridisation and nucleotide sequencing. Prior to sequencing, an agarose gel and a denaturing gradient gel Electrophoresis profile were determined for each isolate. The various techniques were optimised specifically for the filamentous isolates. The isolates were identified as Gordonia amarae, Haliscomenobacter hydrossis, Acinetobacter sp./Type 1863, Type 021N, Thiothrix nivea, Sphaerotilus natans and Nocardioform organisms.