Pawpaw (Asimina triloba (L.) Dunal) has significant potential as a new fruit crop. During ripening, loss of firmness is extremely rapid, and this trait may be the biggest obstacle to the development of a broader market as handling without injury is difficult. Cold storage of pawpaw seems limited to 4 weeks at 4 C. A study of several cultivars with commercial appeal showed that ripening traits such as ethylene production, respiration and loss of firmness were similar in all genotypes, and that no cultivar showed superior responses to cold storage. Cold storage for longer than 4 weeks caused the development of cold injury symptoms such as black discoloration, rapid loss of firmness, impaired respiration, tissue acidification, decrease in antioxidant content, decrease in volatile ester production and development of off-flavor volatile compounds. Overall cold storage injury symptoms observed in pawpaw may be due to oxidative damage linked to the failure of the two major antioxidant systems that could protect against such damage: phenolics and the ascorbateglutamate system. With the aim of enhancing pawpaw low temperature tolerance and prolonging cold storage length, different techniques such as hot air exposure and hot water dips of fruit prior to beginning cold storage, and intermittent warming periods during cold storage, were evaluated. Despite positive results with these techniques for other commodities, all the strategies failed to appreciably alter fruit ripening, loss of firmness or maintain fruit quality during and/or after cold storage.

We aimed to identify the volatile compounds in inflorescences of Rudbeckia hirta that may be responsible for the olfactory attraction of the crab spider Misumenoides formosipes to this plant. Our approach was to use ultrasonic extraction, separate the extract into fractions using flash chromatography with different solvent systems, and test the attraction of the male spiders to the pooled fractions using a y-tube olfactometer. Ultrasonic extraction is carried out using a mixture of 1:2 hexane/diethyl ether with 10 g of inflorescences for 30 minutes. Bioassay results indicated that male spiders chose the inflorescences, bulk ultrasonic extract, and the pooled 100% dichloromethane fractions over controls. Nuclear magnetic resonance experiments and infrared spectroscopy experiments were carried out on the 100% dichloromethane fractions and these experiments indicated that a long chain hydrocarbon is the main component in the 100% dichloromethane fractions / Chromatographic method and bioassay development method -- M. formosipes olfactory response to R. hirta -- Separation and identification of the possible attractants in the 100% dichloromethane fractions. / Department of Chemistry

Volatile organic compounds (VOCs) are emitted into the atmosphere from biogenic and anthropogenic sources with atmospheric lifetimes ranging from minutes to months, depending on the specific VOC compound considered. It is estimated that biogenic VOCs (BVOCs) (e.g. isoprenes, terpenes) make up 90% of the global atmospheric VOC budget. However, in highly industrialised regions, anthropogenic VOCs (e.g. benzene, toluene, ethylbenzene and xylene, combined abbreviated as BTEX) might dominate. VOCs have various reversible and irreversible effects on human health. They also have environmental impacts that range from changes in the population of terrestrial and aquatic ecosystems to the extinction of vulnerable species. VOCs are precursors for the formation of ozone (O3) during solar radiation initiated reactions in the presence of NOx. Tropospheric O3 is considered a pollutant, with negative impacts on human health, ecosystems and food security. O3 is also a short-lived greenhouse gas. Through reactions with radical species, VOCs lead to the formation of higher molecular weight organic compounds, which produce carbon monoxide (CO), peroxyacytyl nitrate (PAN) and ultimately secondary organic aerosol (SOA) particles. SOA particles impact directly on air quality and visibility, as well as directly and indirectly on the radiation balance of the earth that contributes to the regulation of climate. Notwithstanding the importance of atmospheric VOCs, limited data is available for VOCs in South Africa. In this study, a comprehensive dataset of BVOC and anthropogenic VOC species was obtained at the Welgegund measurement station in the North West Province, South Africa. Measurements were conducted from 9 February 2011 to 4 February 2012. Samples were collected on Tenax-TA and Carbopack-B adsorption tubes twice a week for two hours during day time and two hours during night time. The first 1.25m of the stainless steel sampling inlet was heated to 120ºC to remove O3 that could lead to sample degradation. Analyses of the sampled adsorption tubes were conducted by thermal desorption, cryofocusing, re-desorption, followed by gas chromatography separation and analysis with a mass selective detector (GC-MS). The results indicated that toluene was the most abundant aromatic hydrocarbon and heptane the most abundant alkane. Benzene is currently the only VOC listed as a criteria pollutant in the South African Air Quality Act with an annual average standard of 1.6ppb. The annual median benzene concentration was 0.13 ppb, while the highest daily benzene concentration measured was 8.7 ppb. No distinct seasonal cycles were identified for anthropogenic VOC species measured, i.e. aromatic hydrocarbons and alkanes. However, air mass history analysis indicated that air masses that passed over the Mpumalanga Highveld, the Vaal Triangle and the Johannesburg-Pretoria conurbation (collectively referred to as Area I) had significantly higher concentrations of these anthropogenic VOCs compared to air masses that passed over the western and eastern Bushveld Igneous Complex, and a region over which air masses typically followed an anti-cyclonic movement pattern (collectively referred to as Area II). Anthropogenic VOC levels in air masses that passed over the regional background (areas with no large point sources) had levels similar to air masses that had passed over Area II. Relatively good interspecies correlations (r > 0.8) between most of the aromatic hydrocarbons in air masses that had passed over Area I, with the exception of benzene, indicated that these species had common sources. Benzene, however, correlated well with CO, indicating that sources associated with incomplete combustion were most likely the origin of benzene in air masses that had passed over Area I. The interspecies concentration ratios for plumes passing over Area I indicated that this source region is relatively close to the Welgegund monitoring station and air masses that passed over this source region were substantially influenced by anthropogenic activities. The concentration ratios for plumes that passed over Area II and the Regional Background indicated that these were aged air masses. Furthermore, the concentration ratios of toluene, ethylbenzene and o,m,p-xylene (TEX) to the total aromatic concentration for air masses that passed over the various source regions showed a greater contribution to the total VOC concentration during periods of higher temperature, i.e. summer. This proved that the evaporation of solvents contributes significantly to VOC levels during the months with higher temperatures. The relative contribution of aromatic hydrocarbons to photochemical O3 formation in air masses that passed over the various source regions indicated the highest contribution was observed for air masses that passed over Area I, with Area II and the Regional Background in the same order of magnitude. The annual temporal variations of the measured BVOCs indicated that 2-methyl-3-buten-2-ol (MBO) and isoprene exhibited distinct seasonal patterns, i.e. higher values in summer and lower values in winter. The monoterpenes (MT) and the sesquiterpenes (SQT) did not follow distinct seasonal patterns. BVOC concentrations correlated relatively well to seasonal variations in temperature, photosynthetically active radiation (PAR), rainfall, relative humidity (RH) and CO2 flux. This proved that biogenic activity is responsible for BVOCs emitted. The most abundant MT was -pinene, while -caryophyllene was the most abundant SQT with annual median concentrations of 0.468 ppb and 0.022 ppb, respectively. Pollution roses for isoprene showed a dominance of sources from the north-west to the north-east, as well as the south-east. These directions correlated to areas where pockets of the savannah biome are located. / Thesis (MSc (Environmental Sciences))--North-West University, Potchefstroom Campus, 2013

Volatile organic compounds (VOCs) are emitted into the atmosphere from biogenic and anthropogenic sources with atmospheric lifetimes ranging from minutes to months, depending on the specific VOC compound considered. It is estimated that biogenic VOCs (BVOCs) (e.g. isoprenes, terpenes) make up 90% of the global atmospheric VOC budget. However, in highly industrialised regions, anthropogenic VOCs (e.g. benzene, toluene, ethylbenzene and xylene, combined abbreviated as BTEX) might dominate. VOCs have various reversible and irreversible effects on human health. They also have environmental impacts that range from changes in the population of terrestrial and aquatic ecosystems to the extinction of vulnerable species. VOCs are precursors for the formation of ozone (O3) during solar radiation initiated reactions in the presence of NOx. Tropospheric O3 is considered a pollutant, with negative impacts on human health, ecosystems and food security. O3 is also a short-lived greenhouse gas. Through reactions with radical species, VOCs lead to the formation of higher molecular weight organic compounds, which produce carbon monoxide (CO), peroxyacytyl nitrate (PAN) and ultimately secondary organic aerosol (SOA) particles. SOA particles impact directly on air quality and visibility, as well as directly and indirectly on the radiation balance of the earth that contributes to the regulation of climate. Notwithstanding the importance of atmospheric VOCs, limited data is available for VOCs in South Africa. In this study, a comprehensive dataset of BVOC and anthropogenic VOC species was obtained at the Welgegund measurement station in the North West Province, South Africa. Measurements were conducted from 9 February 2011 to 4 February 2012. Samples were collected on Tenax-TA and Carbopack-B adsorption tubes twice a week for two hours during day time and two hours during night time. The first 1.25m of the stainless steel sampling inlet was heated to 120ºC to remove O3 that could lead to sample degradation. Analyses of the sampled adsorption tubes were conducted by thermal desorption, cryofocusing, re-desorption, followed by gas chromatography separation and analysis with a mass selective detector (GC-MS). The results indicated that toluene was the most abundant aromatic hydrocarbon and heptane the most abundant alkane. Benzene is currently the only VOC listed as a criteria pollutant in the South African Air Quality Act with an annual average standard of 1.6ppb. The annual median benzene concentration was 0.13 ppb, while the highest daily benzene concentration measured was 8.7 ppb. No distinct seasonal cycles were identified for anthropogenic VOC species measured, i.e. aromatic hydrocarbons and alkanes. However, air mass history analysis indicated that air masses that passed over the Mpumalanga Highveld, the Vaal Triangle and the Johannesburg-Pretoria conurbation (collectively referred to as Area I) had significantly higher concentrations of these anthropogenic VOCs compared to air masses that passed over the western and eastern Bushveld Igneous Complex, and a region over which air masses typically followed an anti-cyclonic movement pattern (collectively referred to as Area II). Anthropogenic VOC levels in air masses that passed over the regional background (areas with no large point sources) had levels similar to air masses that had passed over Area II. Relatively good interspecies correlations (r > 0.8) between most of the aromatic hydrocarbons in air masses that had passed over Area I, with the exception of benzene, indicated that these species had common sources. Benzene, however, correlated well with CO, indicating that sources associated with incomplete combustion were most likely the origin of benzene in air masses that had passed over Area I. The interspecies concentration ratios for plumes passing over Area I indicated that this source region is relatively close to the Welgegund monitoring station and air masses that passed over this source region were substantially influenced by anthropogenic activities. The concentration ratios for plumes that passed over Area II and the Regional Background indicated that these were aged air masses. Furthermore, the concentration ratios of toluene, ethylbenzene and o,m,p-xylene (TEX) to the total aromatic concentration for air masses that passed over the various source regions showed a greater contribution to the total VOC concentration during periods of higher temperature, i.e. summer. This proved that the evaporation of solvents contributes significantly to VOC levels during the months with higher temperatures. The relative contribution of aromatic hydrocarbons to photochemical O3 formation in air masses that passed over the various source regions indicated the highest contribution was observed for air masses that passed over Area I, with Area II and the Regional Background in the same order of magnitude. The annual temporal variations of the measured BVOCs indicated that 2-methyl-3-buten-2-ol (MBO) and isoprene exhibited distinct seasonal patterns, i.e. higher values in summer and lower values in winter. The monoterpenes (MT) and the sesquiterpenes (SQT) did not follow distinct seasonal patterns. BVOC concentrations correlated relatively well to seasonal variations in temperature, photosynthetically active radiation (PAR), rainfall, relative humidity (RH) and CO2 flux. This proved that biogenic activity is responsible for BVOCs emitted. The most abundant MT was -pinene, while -caryophyllene was the most abundant SQT with annual median concentrations of 0.468 ppb and 0.022 ppb, respectively. Pollution roses for isoprene showed a dominance of sources from the north-west to the north-east, as well as the south-east. These directions correlated to areas where pockets of the savannah biome are located. / Thesis (MSc (Environmental Sciences))--North-West University, Potchefstroom Campus, 2013

During storage of grain, there may have significant damage to its quality due to unfavorable physical and biological interactions and thus requires continuous monitoring. Therefore, an easy, cost-effective and environmentally friendly method is necessary for efficient monitoring of stored-grain. Arrays of sensors are being used for classifying liquors, perfumes, quality of food products mimicking mammalian olfactory systems. Monitoring of stored grain is a new application of sensor arrays. The main objective was to fabricate a carbon black polymer sensor array which can easily monitor incipient grain spoilage by detecting spoiling stored grain volatiles (benzene derivatives and aliphatic hydrocarbon derivatives) with minimum interference from relative humidity. Various aspects of a good sensor were analyzed using statistical analysis (RSD, LDA, PCA, t-test). The developed sensor array can identify red flour beetle-infected and uninfected wheat and fungal volatiles at ambient conditions as well as some stored grain conditions (MC 16%, RH 52%).

Detecting the presence of insects at low densities can avoid total deterioration of stored grains because corrective actions can be implemented early. Tribolium castaneum (Herbst) and Cryptolestes ferrugineus (Stephens) are the major insect pests of the Canadian grain handling industry. Identification of the volatile organic compounds released by insects can be used to detect insects in stored grains. An attempt was made to identify the volatile organic compounds released by T. castaneum and C. ferrugineus by headspace analysis. The volatiles in the head space of vials with insects, insects and wheat flour, and insects and wheat, were analyzed using a GC-MS coupled with an automatic headspace sampler. Wheat with fifteen percent moisture content was used in this study along with two different insect densities. Feasibility of the automatic headspace sampler in headspace analysis was found to be positive. The sampler can do sample conditioning, absorption, trap cleaning and desorption of the volatiles into the GC-MS and speed up the process. The samples extracted at 20 strokes with 1000 µL per stroke, and desorbed at 250°C gave a clear peak of compounds. The amount of volatiles produced by T. castaneum adults varied based on insect densities, the concentration of Methyl-1, 4-benzoquinone; Ethyl-1, 4-benzoquinone; and 1-Tridecene released by ten adult insects were 355, 390 and 530 µg/L compared to 300,310 and 210 µg/L of Methyl-1, 4-benzoquinone; Ethyl-1, 4-benzoquinone; and 1-Tridecene produced by five adult insects. Extreme high and low temperature leading to death produced very high amounts of volatiles compared to insects kept at 35°C. The larvae of the T. castaneum insects did not produce any volatiles at ambient condition as well as at extreme cold and warm conditions. The C. ferrugineus adults did not produced any detectable amount of volatiles even at the higher insect density after up to 3 days. The results of the combination of T. castaneum and C. ferrugineus insects gave the same volatile organic compounds as produced by T. castaneum insects alone. The 1-Tridecene produced by T. castaneum was not reported previously in other studies.

Bibliography: leaves 322-335. / xxxvii, 343 leaves : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Highlights the need for extensive testing of large particle coal devolatilization models with both volatile matter evolution and particle temperature data in order to ensure that the predictions generated by the model can be thoroughly trusted. By undertaking an in-depth investigation into the particle temperature measurements and associated model predictions, shows that accurate model predictions can be obtained for the evolution of volatile matter, and of individual volatile species. The model is also capable of predicting the behaviour of wet coal particles by assuming that drying is heat transfer controlled and that the enthalpy of drying observed by Chen is applicable. Ultimately, this model forms a sound basis for the on-going development of a model encompassing all of the reactions required to model the behaviour of a typical coal particle in a fluidished bed combustor or gasifier. / Thesis (Ph.D.)--University of Adelaide, Dept. of Chemical Engineering, 1999

Bibliography: leaves 322-335. / xxxvii, 343 leaves : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Highlights the need for extensive testing of large particle coal devolatilization models with both volatile matter evolution and particle temperature data in order to ensure that the predictions generated by the model can be thoroughly trusted. By undertaking an in-depth investigation into the particle temperature measurements and associated model predictions, shows that accurate model predictions can be obtained for the evolution of volatile matter, and of individual volatile species. The model is also capable of predicting the behaviour of wet coal particles by assuming that drying is heat transfer controlled and that the enthalpy of drying observed by Chen is applicable. Ultimately, this model forms a sound basis for the on-going development of a model encompassing all of the reactions required to model the behaviour of a typical coal particle in a fluidished bed combustor or gasifier. / Thesis (Ph.D.)--University of Adelaide, Dept. of Chemical Engineering, 1999

Thesis (M.S. - Hydrology and Water Resources)--University of Arizona. / Includes bibliographical references (leaves 270-273).

Thesis (Ph. D.)--University of Nevada, Reno, 2006. / "August, 2006." Includes bibliographical references (leaves xx-xx). Online version available on the World Wide Web.