This thesis investigates the relationship between success and access to children, slaves, and kin as labor sources during the period of 1833 to 1865 in northeast Mississippi. The theoretical concepts of agricultural intensification and relative intensity were used to measure variability among the households. Artifacts from seven archaeological sites were used to establish mean dates. These sites were tied to their original occupants through historic records. A historic document search revealed the number of slaves and children each family had, and whether they had kin living nearby. Agricultural census records showed the productivity of each farm during the study period. Families were considered successful if they stayed in the study area until death, increased the number of slaves or land owned, or increased their agricultural output. This thesis concluded that the relationship between success and the availability of labor is complex with no one strategy ensuring success.

Three studies regarding Escherichia coli O157:H7 in apple cider were conducted. The objectives were: to evaluate the effectiveness of wash and sanitizers for removing E. coli O157:H7 from apples; to survey cider producer practices; and to determine the efficacy of ultraviolet light for reducing E. coli O157:H7 in cider. Apples with a five-strain acid resistant mixture of E. coli O157:H7 were treated with 200 ppm hypochlorite, a phosphoric acid-based fruit wash, 5% acetic acid, 5% acetic acid followed by 3% hydrogen peroxide, a peroxyacetic acid-based solution, and distilled water. The water wash caused insignificant reductions. All other treatments caused significant reductions. Acetic acid and peroxyacetic acid were the most effective with reductions of 3.1 and 2.6 logs, respectively. The survey determined that most producers are small, seasonal operations. Most use sound orchard management practices, clean and sanitize daily, sort and wash apples, use refrigeration, and try to prevent contamination. However, some use drop and damaged apples. Few use chemical sanitizers on apples, preservatives, pasteurize cider, or have HACCP programs. Cider inoculated with the same mixture of E. coli O157:H7 was processed using a thin- film ultraviolet disinfection unit operating at 254 nm. Dosages ranged from 9,402 to 61,005 æW- sec/cm2. Treatment significantly reduced E. coli O157:H7 (pó 0.0001) with a mean reduction of 3.81 log CFU/ml. Reduction was also affected by the level of background microflora in cider. Results indicate that ultraviolet light can reduce this pathogen in cider. However, additional reduction measures are necessary to achieve the required 5 log reduction. / Master of Science

Ultraviolet light (UV) and hydrogen peroxide (H2O2) decrease eggshell bacteria. However, when combined, the optimum amount of each and effects on hatchability are unknown. In Experiment 1, when compared to other concentrations of H2O2 and lengths of UV, the combination of 1.5% H2O2 and 8 minutes of UV yielded optimum results with a 3 log10 CFU/egg reduction in bacteria on the eggshell. In Experiment 2, exposing eggs to this optimum combination yielded a 1000 fold reduction in eggshell bacteria but only a numerical increase in hatch of set and hatch of fertile. In Experiment 3, eggs exposed to repetitive treatments of H2O2 and UV yielded a 4 log reduction in eggshell bacteria but no differences in hatchability or chick characteristics. In conclusion, the combination of H2O2 and UV proved to be effective for eggshell sanitization, especially when used repetitively, and did not alter hatchability.

No description available.

This research investigated the efficacy of chlorine dioxide (ClO₂), ultraviolet (UV) irradiation, UV in combination with chlorine dioxide (UV/ClO₂), and UV in combination with hydrogen peroxide (UV/H₂O₂) for decolorizing three reactive azo dyes (sultan red, indigo blue and cypress green) and treated textile-manufacturing wastewater. The objective was to determine the best treatment for reducing color to the Virginia Pollutant Discharge Elimination System (VPDES) permit level of 300 American Dye Manufacturers Institute (ADMI) units. The effects of the three chemical oxidation treatments provided color reduction for all three dyes. The results suggested UV/H₂O₂ and UV/ClO₂2 treatments provided maximum color reduction of the red and blue dyes, and UV/H₂O₂ was the most effective for maximum reduction of the green dye. A research goal was to provide predictive models of the wastewater effluent for the treatment processes, including the UV exposure time required to reach the 300 ADMI permit value and the effective ClO₂ dose necessary to achieve the 300 units. The results of the investigations regarding the effluent indicated that UV/H₂O₂ and UV/ClO₂ (5 mg/L) provided reduction to 300 units in less than 10 minutes UV exposure when the initial effluent color was less than 500 ADMI units. Without the addition of oxidant, contact times longer than 10 minutes were required for UV to decolorize these effluents to 300 ADMI units. Chlorine dioxide dosages between 10 and 30 mg/L both with and without UV irradiation achieved the same results. / Master of Science

Ready-to-eat meat products have been implicated in several foodborne listeriosis outbreaks. Microbial contamination of these products can occur after the product has been thermally processed and is being rapidly chilled using salt brines. The objective of this study was to determine the effect of ultraviolet irradiation on the inactivation of Listeria monocytogenes and lactic acid bacteria in a model brine chiller system. Two concentrations of brines (7.9%w/w or 13.2%w/w) were inoculated with a ~6.0 log10 CFU/ml cocktail of L. monocytogenes or lactic acid bacteria and passed through the ultraviolet (UV) treatment system for 60 minutes. Three replications of each bacteria and brine combination were performed and resulted in at least a 4.5 log reduction in microbial numbers in all treated brines after exposure to ultraviolet light. Bacterial populations were significantly reduced after five minutes exposure to UV light in the model brine chiller as compared to the control, which received no UV light exposure (P<0.05). The maximum rate of inactivation for both microorganisms in treated brines occurred between minute 1 and 15 of ultraviolet exposure. Overall, results indicate that inline treatment of chill brines with ultraviolet light (UVC) shows promise in inactivating L. monocytogenes and lactic acid bacteria. Due to the low capital involved in initiating a continuous inline UV system, the use of ultraviolet energy may prove to be beneficial for effectively controlling pathogens in recycled chill brines without interrupting the chilling operation. An inline ultraviolet system could be used in a hazard analysis and critical control points plan. / Master of Science

This study presents findings on the effect of domestic laundry detergents on the fastness to light of selected fibre reactive dyes applied to cotton. The study was carried out to elucidate the reasons for the accelerated colour loss of cotton garments washed under Australian domestic laundering conditions. Cotton fabric dyed with commonly used reactive dyes were laundered with water only, several domestic detergents and a laboratory formulated neutral detergent, and then exposed to light for two hours in the wet state. Quantities of detergent used were in accordance with the manufacturers recommendations. Exposures were repeated fifteen times equivalent to 30 hours exposure. Colour loss and colour difference were measured after 5, 10 and 15 wash cycles and 10, 20 and 30 hours exposure. When the fabric was exposed wet the colour faded more rapidly than when exposed dry to light. Detergents increased the colour loss even when the fabric was not exposed to light. The presence of an oxidizing bleach (sodium perborate) in the detergent increased colour loss during washing and wet exposure to light. Ultraviolet radiation from the light source, heat, moisture, alkali and oxidising bleach during exposure resulted in hydrolysis of the dye-fibre bond causing dye desorption during washing and rinsing. Water alone increased the fading of the dyes most likely due to presence of dissolved oxygen held within the fibre. The combination of ultraviolet radiation and oxidizing bleaches altered the chemistry of the dye and hence its shade. This was particularly evident on the black dye and one of the navy blue dyes.

<p>In diploid yeast cells, mitotic recombination is very important for repairing double-strand breaks (DSB). When repair of a DSB results in crossovers, it may cause loss of heterozygosity (LOH) of markers centromere-distal to the DSB in both daughter cells. Gene conversion events unassociated with crossovers cause LOH for an interstitial section of a chromosome. Alternatively, DSBs can initiate break-induced replication (BIR), causing LOH in only one of the daughter cells. Mapping mitotic LOH contributes to understanding of mechanisms for repairing DSBs and distribution of these recombinogenic lesions. Methods for selecting mitotic crossovers and mapping the positions of crossovers have recently been developed in our lab. Our current approach uses a diploid yeast strain that is heterozygous for about 55,000 SNPs, and employs SNP-Microarrays to map LOH events throughout the genome. These methods allow us to examine selected crossovers on chromosome V and unselected mitotic recombination events (crossovers, gene conversion events unassociated with crossovers, and BIR events) at about 1 kb resolution across the genome.</p><p>Mitotic recombination can be greatly induced by UV radiation. However, prior to my research, the nature of the recombinogenic lesions and the distribution of UV-induced recombination events were relatively uncharacterized. Using SNP microarrays, we constructed maps of UV-induced LOH events in G1-synchronized cells. Mitotic crossovers were stimulated 1500-fold and 8500-fold by UV doses of 1 J/m2 and 15 J/m2, respectively, compared to spontaneous events. Additionally, cells treated with 15 J/m2 have about eight unselected LOH events per pair of sectors, including gene conversions associated and unassociated with crossovers as well as BIR events. These unselected LOH events are distributed randomly throughout the genome with no particular hotspots; however, the rDNA cluster was under-represented for the initiation of crossover and BIR events. Interestingly, we found that a high fraction of recombination events in cells treated with 15 J/m2 reflected repair of two sister chromatids broken at roughly the same position. In cells treated with 1 J/m2, most events reflect repair of a single broken sister chromatid (Chapter 2). </p><p>The primary pathway to remove pyrimidine dimers introduced by UV is the nucleotide excision repair (NER) pathway. In NER, the dimer is excised to generate a 30-nucleotide gap that can be replicated to form DSBs if not filled in before DNA replication. The NER gap can also be expanded by Exo1p to form single stranded gaps greater than one kilobase. Alternatively, in the absence of NER, unexcised dimers could result in blocks of DNA replication forks. Resolving the stalled replication fork could lead to recombinogenic breaks. In Chapter 3 and Chapter 4, we analyzed recombination events in strains defective in various steps of processing of UV-induced DNA damage, including exo1 and rad14 mutants. </p><p>In Chapter 3, I show that Exo1p-expanded NER gaps contribute to UV-induced recombination events. Interestingly, I also found that Exo1p is also required for the hotspot activity of a spontaneous crossover hotspot involving a pair of inverted Ty repeats. In addition to its role of expanding a nick to a long single-stranded gap, Exo1p is also a major player in DSB end resection. Therefore, I examined the gene conversion tract lengths in strains deleted for EXO1. I found that, although crossover-associated gene conversion tracts become shorter in the exo1 mutant as expected, noncrossover tract lengths remained unaffected. As a result, noncrossover tracts are longer than crossover tracts in the exo1 mutant while the opposite result was observed in the wild-type strains. I proposed models to rationalize this observation.</p><p>In Chapter 4, to investigate whether the substantial recombinogenic effect in UV in G1-synchronized cells requires NER, we mapped UV-induced LOH events in NER-deficient rad14 diploids treated with 1 J/m2. Mitotic recombination between homologs was greatly stimulated, which suggests that dimers themselves can also cause recombination without processing by NER. We further show that UV-induced inter-homolog recombination events (noncrossover, crossover and BIR) depend on the resolvase Mus81p, and are suppressed by Mms2p-mediated error-free post-replication repair pathway. </p><p>The research described in Chapters, 2, 3, and 4 are in the publications Yin and Petes (2013), Yin and Petes (2014), and Yin and Petes (2015), respectively.</p> / Dissertation

The interaction of intense laser pulses with nanometer scale atomic clusters has been an active area of study since the advent of amplified femtosecond lasers. In the case of infrared irradiation of noble gas clusters, direct field-driven ionization results in the ejection of energetic electrons, high ion charge states, and Coulomb explosion of the ion core of the clusters. These processes result from electron motion driven by the cluster potential and the large ponderomotive potential of the laser field. When extreme ultraviolet (XUV) pulses interact with clusters, the mechanisms responsible for the infrared response are 'turned off' because the ponderomotive potential is very small. We have conducted cluster experiments at 38nm using focused XUV pulses produced by high harmonic generation with a 15TW Ti:Sapphire laser. We measured the charge states and kinetic energy spectra of ions produced in the interaction, and observe substantial ion population up to Xe⁵⁺, with a small number of Xe⁶⁺-Xe⁸⁺ ions produced by collisional ionization by hot plasma electrons. The ion kinetic energy spectrum indicates a hydrodynamic expansion at an ion temperature of 8eV. This is in stark contrast to intense infrared/cluster interactions, where clusters are stripped of electrons to a large degree and expand by Coulomb forces, resulting in far higher ion kinetic energy for similar degrees of ionization. / text

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第20702号 / 工博第4399号 / 新制||工||1683(附属図書館) / 京都大学大学院工学研究科材料工学専攻 / (主査)教授 杉村 博之, 教授 河合 潤, 教授 邑瀬 邦明 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM