Doctor of Philosophy (PhD) / The goal of this research was to test commercially viable alternative methods to fungicides for controlling storage diseases of melons that are safe for human health and the environment. Initially, experiments were conducted on melons to develop a protocol for optimum conditions of disease development during storage for different pathogens and for different stages of fruit maturity. For all pathogens tested, the study found that humidity greater than 90% and temperatures above 20° C support infection and rapid growth of disease. Differences in the rate of infection and extent of disease development after the inoculation of different storage pathogens was observed between rockmelon and honeydew melons, indicating differences in host pathogen interactions. Among the tested pathogens, Alternaria spp. was the least aggressive in infection and disease severity, growing considerably slower than Fusarium acuminatum which was moderately aggressive and Rhizopus spp. which was very aggressive, in comparison. Green half-slip melons showed greater resistance to pathogen attack than green full-slip fruit, while yellow full-slip melons were highly susceptible to pathogen attack. Therefore, the laboratory experiments for postharvest treatments of rockmelons were performed using green full-slip fruit challenged with F. acuminatum. Evaluation of physical and safe chemical methods of postharvest treatment to control postharvest diseases of melons showed that none of the treatments alone was as effective as the commercially available fungicide. Hot water solutions of safe compounds considerably increase their efficacy against postharvest rots, however, symptoms of phytotoxicity on the rind after dipping made their use unacceptable. Iodine was the only safe chemical tested which did not cause any phytotoxicity on melons. When combined with hot water, iodine showed the best control of storage rots and was as good as the fungicides carbendazim or guazatine. Hot water iodine dipping of fruit also delayed ripening and fruit were firmer during storage for a longer period of time. Systemic acquired resistance (SAR) was evaluated as a method of controlling powdery mildew in glasshouse grown rockmelon seedlings by treating with the activators 2,6-dichloroisonicotinic acid (INA) or benzothiadiazole (BTH) or water. Increased resistance due to application of INA or BTH, was observed by the reduction of powdery mildew on pre-inoculated detached leaves and also on intact leaves from natural infections. Heightened resistance due to spraying with elicitors of SAR, was further evident by the increased activities of the pathogenesis related proteins (PR proteins), peroxidase and accumulation of phenolics or antifungal compounds during and after challenge inoculation. Field grown rockmelons were treated with INA or BTH or BABA (β-aminobutyric acid) or water at various stages of plant growth and evaluated for increased resistance against pre and postharvest diseases. Both powdery mildew and downy mildew were significantly less on the SAR elicitor treated plants. Preharvest treatment with SAR elicitors also reduced storage diseases of the harvested rockmelon fruit. The reduction in postharvest disease was similar whether plants were treated once, three weeks before harvest, or given four sprays during the growing season beginning at anthesis. A further postharvest dip with 500 ppm of guazatine gave substantial reduction of storage rots of melons. Enhanced activities of chitinase and peroxidase, two major PR-proteins, compared to the control, indicated induction of defence had occurred in the foliage and fruit as a result of SAR. Over the course of four field and one glasshouse experiments slight phytotoxicity was observed in plants frequently sprayed with INA or BTH, but no phytotoxicity was seen after a single spray during the late stages of fruit development. The combination of SAR elicitor treatment and use of a safe postharvest dip provided substantial control of storage rots of rockmelons. The best treatment for control of storage rots involved application of BTH (50 ppm) two weeks before harvest, combined with a hot iodine dip (55° C) of fruit, achieving equivalent or better disease control than use of guazatine fungicide dip.

Doctor of Philosophy (PhD) / The goal of this research was to test commercially viable alternative methods to fungicides for controlling storage diseases of melons that are safe for human health and the environment. Initially, experiments were conducted on melons to develop a protocol for optimum conditions of disease development during storage for different pathogens and for different stages of fruit maturity. For all pathogens tested, the study found that humidity greater than 90% and temperatures above 20° C support infection and rapid growth of disease. Differences in the rate of infection and extent of disease development after the inoculation of different storage pathogens was observed between rockmelon and honeydew melons, indicating differences in host pathogen interactions. Among the tested pathogens, Alternaria spp. was the least aggressive in infection and disease severity, growing considerably slower than Fusarium acuminatum which was moderately aggressive and Rhizopus spp. which was very aggressive, in comparison. Green half-slip melons showed greater resistance to pathogen attack than green full-slip fruit, while yellow full-slip melons were highly susceptible to pathogen attack. Therefore, the laboratory experiments for postharvest treatments of rockmelons were performed using green full-slip fruit challenged with F. acuminatum. Evaluation of physical and safe chemical methods of postharvest treatment to control postharvest diseases of melons showed that none of the treatments alone was as effective as the commercially available fungicide. Hot water solutions of safe compounds considerably increase their efficacy against postharvest rots, however, symptoms of phytotoxicity on the rind after dipping made their use unacceptable. Iodine was the only safe chemical tested which did not cause any phytotoxicity on melons. When combined with hot water, iodine showed the best control of storage rots and was as good as the fungicides carbendazim or guazatine. Hot water iodine dipping of fruit also delayed ripening and fruit were firmer during storage for a longer period of time. Systemic acquired resistance (SAR) was evaluated as a method of controlling powdery mildew in glasshouse grown rockmelon seedlings by treating with the activators 2,6-dichloroisonicotinic acid (INA) or benzothiadiazole (BTH) or water. Increased resistance due to application of INA or BTH, was observed by the reduction of powdery mildew on pre-inoculated detached leaves and also on intact leaves from natural infections. Heightened resistance due to spraying with elicitors of SAR, was further evident by the increased activities of the pathogenesis related proteins (PR proteins), peroxidase and accumulation of phenolics or antifungal compounds during and after challenge inoculation. Field grown rockmelons were treated with INA or BTH or BABA (β-aminobutyric acid) or water at various stages of plant growth and evaluated for increased resistance against pre and postharvest diseases. Both powdery mildew and downy mildew were significantly less on the SAR elicitor treated plants. Preharvest treatment with SAR elicitors also reduced storage diseases of the harvested rockmelon fruit. The reduction in postharvest disease was similar whether plants were treated once, three weeks before harvest, or given four sprays during the growing season beginning at anthesis. A further postharvest dip with 500 ppm of guazatine gave substantial reduction of storage rots of melons. Enhanced activities of chitinase and peroxidase, two major PR-proteins, compared to the control, indicated induction of defence had occurred in the foliage and fruit as a result of SAR. Over the course of four field and one glasshouse experiments slight phytotoxicity was observed in plants frequently sprayed with INA or BTH, but no phytotoxicity was seen after a single spray during the late stages of fruit development. The combination of SAR elicitor treatment and use of a safe postharvest dip provided substantial control of storage rots of rockmelons. The best treatment for control of storage rots involved application of BTH (50 ppm) two weeks before harvest, combined with a hot iodine dip (55° C) of fruit, achieving equivalent or better disease control than use of guazatine fungicide dip.

Choi Yin Yee. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2001. / Includes bibliographical references (leaves 164-187). / Abstracts in English and Chinese. / List of Abbreviations / List of Tables / List of Figures / Chapter Chapter 1: --- "Background of straw mushroom, Volvariella volvacea" / Chapter 1.1 --- History and economic value of straw mushroom --- p.1 / Chapter 1.2 --- Nutritional value and medical use of straw mushroom --- p.2 / Chapter 1.3 --- Cultivation of straw mushroom --- p.3 / Chapter 1.4 --- Life cycle and developmental stages of straw mushroom --- p.5 / Chapter 1.5 --- Objectives of the research --- p.6 / Chapter Chapter 2: --- Determination of straw mushroom quality during postharvest storage / Chapter 2.1 --- Introduction --- p.18 / Chapter 2.2 --- Materials and methods / Chapter 2.2.1 --- Determination of surface color changes --- p.19 / Chapter 2.2.2 --- Determination of weight loss and dry weight --- p.19 / Chapter 2.2.3 --- Examination of mushroom surface structure --- p.20 / Chapter 2.2.4 --- Statistical analysis --- p.20 / Chapter 2.3 --- Results and discussion / Chapter 2.3.1 --- Browning during postharvest storage --- p.20 / Chapter 2.3.2 --- Weight loss and dry weight changes during storage --- p.22 / Chapter 2.3.3 --- Surface structural changes during postharvest storage --- p.23 / Chapter Chapter 3: --- Physiological studies of straw mushroom during postharvest storage / Chapter 3.1 --- Introduction --- p.31 / Chapter 3.2 --- Materials and methods / Chapter 3.2.1 --- Materials --- p.33 / Chapter 3.2.2 --- Respiration rates of different produce --- p.34 / Chapter 3.2.3 --- Changes of respiration rate and detection of ethylene production in straw mushroom --- p.34 / Chapter 3.2.4 --- Exogenous ethylene treatment --- p.34 / Chapter 3.3 --- Results and discussion / Chapter 3.3.1 --- Comparative studies of respiration rates between different fresh produce --- p.35 / Chapter 3.3.2 --- Ethylene production and effect of exogenous ethylene effect on straw mushroom --- p.36 / Chapter 3.3.3 --- Change in respiration during postharvest storage --- p.37 / Chapter Chapter 4: --- Biochemical studies of straw mushroom during postharvest storage / Chapter 4.1 --- Introduction / Chapter 4.1.1 --- Hydro lytic enzymes / Chapter 4.1.1.1 --- Protease --- p.43 / Chapter 4.1.1.2 --- Lipase --- p.44 / Chapter 4.1.1.3 --- Chitinase --- p.46 / Chapter 4.1.2 --- Enzymatic browning / Chapter 4.1.2.1 --- Background --- p.48 / Chapter 4.1.2.2 --- Action of polyphenol oxidase --- p.49 / Chapter 4.1.2.3 --- Control of enzymatic browning --- p.50 / Chapter 4.2 --- Materials and methods / Chapter 4.2.1 --- Source --- p.52 / Chapter 4.2.2 --- Enzyme extraction --- p.52 / Chapter 4.2.3 --- Soluble protein determination --- p.52 / Chapter 4.2.4 --- Protease assay --- p.53 / Chapter 4.2.5 --- Lipase assay --- p.53 / Chapter 4.2.6 --- Chitinase assay --- p.54 / Chapter 4.2.7 --- PPO assay --- p.54 / Chapter 4.2.8 --- Optimal pH determination and substrate specificity of PPO --- p.55 / Chapter 4.2.9 --- PPO inhibitors studies --- p.56 / Chapter 4.2.10 --- Localization of PPO in the fruit body of straw mushroom --- p.56 / Chapter 4.3 --- Results and discussion / Chapter 4.3.1 --- Protease activity during postharvest storage --- p.57 / Chapter 4.3.2 --- Lipase activity during postharvest storage --- p.58 / Chapter 4.3.3 --- Chitinase activity during postharvest storage --- p.59 / Chapter 4.3.4 --- pH optimum and substrate specificity of PPO --- p.61 / Chapter 4.3.5 --- PPO activity during postharvest storage --- p.62 / Chapter 4.3.6 --- Effect of various inhibitors on PPO activity --- p.63 / Chapter 4.3.7 --- Localization of PPO in the fruit body of straw mushroom --- p.64 / Chapter Chapter 5: --- Microorganisms in the fruit body of straw mushroom during postharvest storage / Chapter 5.1 --- Introduction --- p.81 / Chapter 5.2 --- Materials and methods / Chapter 5.2.1 --- Evaluation of bacterial population --- p.85 / Chapter 5.2.2 --- Isolation of bacteria --- p.85 / Chapter 5.2.3 --- Treatment of antibacterial agents --- p.87 / Chapter 5.2.4 --- Effect of moisture on bacterial population --- p.87 / Chapter 5.2.5 --- Statistical analysis --- p.87 / Chapter 5.3 --- Results and discussion / Chapter 5.3.1 --- Bacterial population during postharvest storage --- p.88 / Chapter 5.3.2 --- Bacteria growth and mushroom deterioration --- p.89 / Chapter 5.3.3 --- Identification of bacteria isolated from straw mushroom --- p.92 / Chapter 5.3.4 --- Relationship between moisture and bacterial population --- p.95 / Chapter Chapter 6: --- Preservative studies of straw mushroom / Chapter 6.1 --- Introduction --- p.107 / Chapter 6.1.1 --- Chemicals treatment in produce --- p.109 / Chapter 6.1.1.1 --- Application of browning inhibitors --- p.110 / Chapter 6.1.1.2 --- Role of calcium in preservation --- p.111 / Chapter 6.1.2 --- Modified atmosphere technology --- p.114 / Chapter 6.2 --- Materials and methods / Chapter 6.2.1 --- Dipping experiment with browning inhibitors --- p.117 / Chapter 6.2.2 --- Application CaCl2 in straw mushroom cultivation --- p.117 / Chapter 6.2.3 --- Postharvest storage of straw mushroom under modified atmosphere --- p.118 / Chapter 6.2.4 --- Statistical analysis --- p.119 / Chapter 6.3 --- Results and discussion / Chapter 6.3.1 --- Effect of browning inhibitors on mushroom quality --- p.119 / Chapter 6.3.2 --- Effect of calcium chloride on mushroom quality --- p.121 / Chapter 6.3.3 --- Effect of modified atmosphere on mushroom quality --- p.124 / Chapter Chapter 7: --- Conclusion --- p.159 / References --- p.164

Includes bibliographical references (leaves 174-201) / xxii, 201, [20] leaves : ill., photos (col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.)--University of Adelaide, School of Agriculture and Wine, Discipline of Wine and Horticulture, 2004

Typescript (photocopy). / Digitized by Kansas Correctional Industries

Tomato (Lycopersicon esculentum Mill.) is an important commercial crop. High quality tomatoes for the local and export markets are grown hydroponically. In this study, the effect of electrically activated sodium bicarbonate and non-ionized sodium bicarbonate solutions on productivity and postharvest quality of hydroponically grown tomatoes was tested. Sodium bicarbonate is a ready source of bicarbonate. By using a novel technique obtained from Radical Waters (Pty) Ltd., ionized bicarbonate (anolyte) can be produced from sodium bicarbonate and applied to plants to stimulate photosynthesis, and improve yield and postharvest quality. The effect of ionized and non-ionized bicarbonate solutions on productivity and postharvest quality was studied by measuring the following: (1) Preharvest growth rate (leaf length, stem height and diameter); total yield; starch concentration in leaves; fruit count; leaf chlorophyll content; CO2-uptake; soluble solids and concentration of K+, Na+ and NO3¯ in leaves. (2) Postharvest rate of respiration and transpiration; ethylene production; total soluble solids content; ascorbic acid content; pH; fruit firmness; fruit mass; fruit diameter; longevity; concentration of K+, Na+ and NO3¯ at one-third towards maturity, two-thirds towards maturity, at maturity and during ripening, and rate of ripening at 12 and 23°C. During the preharvest period, plants treated with anolyte showed increased growth rate, starch concentration, chlorophyll content, soluble solids content and improved yield. During the growth period, the concentration of K+ and NO3¯ was higher in plants treated with anolyte than in plants treated with non-ionized sodium bicarbonate. The concentration of Na+ during the preharvest period was higher in plants treated with non-ionized sodium bicarbonate than in plants treated with anolyte. After harvest, fruits from plants treated with anolyte had a reduced rate of ethylene production, rate of respiration and transpiration, total increased soluble solids and ascorbic acid content than fruits from plants treated with non-ionized sodium bicarbonate. Fruits from plants treated with anolyte had reduced rate of ripening and were larger and heavier than fruits from plants treated with non-ionized sodium bicarbonate. Anatomical and ultrastructural studies revealed that treatment with anolyte stimulated cell growth and photosynthesis. These results were confirmed by comparing the CO2-uptake of treated and untreated plants. Application of anolyte stimulated photosynthesis, thus improving yield and fruit quality. Treatment with non-ionized sodium bicarbonate resulted in salt- stress and calcium deficiency. Some of the fruits on plants treated with non-ionized sodium bicarbonate suffered from blossom-end rot due to salt-stress. / Prof. C.S. Whitehead

Cowpeas (Vigna unguiculata (L.) Walp) is an important African indigenous legume crop for the livelihoods of many relatively poor people residing n less developed countries of the tropics. Rural families derive a nutritious food, animal feed and in income from the production of this crop. Storage of seed is certainly the most important post-harvest operation but the losses incurred are great. These losses, due to an inability to effectively control physical and biological factors, result in problems with storage insects, moisture and associated fungi. Seeds are particularly susceptible to fungal contamination when stored at high ambient temperatures and relative humidities. To determine the storage fungi associated with cowpea seeds, surface-sterilised cowpea seeds (200 seeds from each of nine cultivars) were plated out n malt extract agar. After 5-7 days incubation at 25°C, the most dominant and common fungi recorded were Alternaria spp. followed by Penicillium spp., Aspergillus flavus and A. niger. The influence of a three-year cold storage period at ± 5°C on the fungi associated with the seeds was also investigated. Alternaria, Aspergillus and Penicillium spp. appeared to dominate. Some fungal species recorded prior to cold storage were not recorded thereafter. Certain storage fungi are known to produce mycotoxins, which are secondary fungal metabolites that are toxic to both farm animals and humans, under poor storage conditions. The presence of the fusarial mycotoxins, fumonisin BI, B2 and B3 in four cowpea cultivars (Bechwana Whit, Glenda, Iron Grey, Rhino) was investigated. The samples were extracted with methanol/water (70:30 v/v) and cleaned-up on strong anion exchange solid phase extraction cartridges. High performance liquid chromatography with pre¬column derivatisation using o-phthaldialdehyde (OPA) was used for the detection and quantification of fumonisin Bl, B2 and B3. All sampIes were contaminated with FBI, with levels ranging from 81-1002 ng g-I. Fumonisin B2 and B3 were not detected in any samples. This is believed to be the first report of fumonisin BI in cowpea seeds. Since the known fumonisin-producing Fusarium species were not found in the six different Fusarium species isolated from these four cultivars, further investigations are required to determine which fungal species are species are responsible species are responsible for the FBI production. An alternative approach to the prevention and control of fungal contamination and mycotoxin production of seeds by treating cowpea seed with essential plant oils was tested. The inhibitory activity of five essential oils (thyme, clove, peppermint, soybean and peanut) was investigated, in vitro and in vivo, on five fungal species (A. flavus, A. niger, Penicillium chrysogenum, Fusarium oxysporum and F. equiseti) commonly associated with cowpea seeds and on two cowpea cultivars. Thyme and clove oil significantly inhibited the growth of all five fungal species in vitro at 500 and 1000 ppm, while peppermint oil was successful at 2000 ppm. Peanut and soybean oil did not show any significant inhibition of fungal growth. The in vivo effect of thyme, clove and peppermint oils on naturally infected seed revealed that only thyme at 1000 ppm reduced fungal growth of storage fungi in the PAN 325 cultivar. In the PAN 311 cultivar, thyme and clove oils at 1000 ppm and peppermint oil at 2000 ppm significantIy reduced growth of storage fungi. In artificially infected seed, all three oils significantly inhibited the growth of P. chrysogenum. Thyme reduced the growth of F. oxysporum and F. equisetii, whilst peppermint oil inhibited only F. oxyspomm. These oils did not seem to adversely affect the germination nor emergence of cowpea seed. The storage fungi significantly reduced percentag germination and emergence of the white (IT 93K452-1) seed but had little or no effect on the brown (CH 14) seed. Furthermore, all three oils significantly inhibited the storage fungi on the white seed, possibly increasing the percentage germination and emergence. / Dissertation (MSc (Botany))--University of Pretoria, 2006. / Plant Science / unrestricted

Dissertation (PhD (Agric))--University of Stellenbosch, 2003. / ENGLISH ABSTRACT: Leaf blackening is a particular problem limiting vase life and marketability of Protea cut flowers. This research investigated suppression of Protea leaf blackening with a specific focus on Protea cv. Sylvia (P. eximia x P. susannae) cut flowers. Leaf blackening decreased significantly with decreasing storage temperatures m 'Sylvia' proteas and this was attributed to lower respiration rate and conservation of carbohydrate. Low storage temperatures were beneficial in short term handling procedures encountered during airfreight. However, use of low temperatures alone during the longer sea freight period was unsatisfactory in either maintaining or extending 'Sylvia' protea vase life. Cooling of 'Sylvia' proteas under vacuum significantly suppressed leaf blackening and was of greater benefit than forced air cooling. Although removal of the uppermost leaves delayed leaf blackening in short term storage no significant benefit was found for longer storage periods. Girdling directly beneath the 'Sylvia' protea flowerhead significantly reduced leaf blackening and in combination with low storage temperatures (O°C) enabled a significant extension in both storage and vase life of 'Sylvia' proteas. 'Sylvia' proteas did not exhibit a climacteric respiration peak during 96 h storage at O°C. Exposure to ethylene did not increase Protea leaf blackening or have a detrimental effect on vase life of either proteas or pincushions evaluated. No beneficial response to sucrose supplementation was found in 'Sylvia' proteas. Analysis of the sugar content of both flowerhead and leaves indicated that glucose supplementation might be of benefit and was investigated. Holding solutions of 2.5 % glucose significantly extended vase life due to a significant reduction in leaf blackening. Vase life was terminated due to flowerhead collapse instead of leaf blackening for the first time in 'Sylvia' protea cut flowers. Vase life was significantly extended by 2:3% glucose pulse solutions and leaf blackening significantly suppressed with increasing glucose pulse concentration. Solution uptake was facilitated by use of high intensity PAR lights in the early morning and was attributed to increased stomata opening and a consequent increase in both transpiration and glucose solution uptake. The faster uptake of glucose solutions in shoots harvested in the afternoon was attributed to higher shoot temperatures and consequent transpiration rate to those harvested in the morning. There was a significant reduction in uptake time with increasing pulse temperature, which enabled vacuum cooling to be performed earlier further benefiting storage and vase life extension. Enclosure of 'Sylvia' proteas in polyethylene (PE) lined cartons did suppress leaf blackening in non-pulsed shoots. However, this had no practical significance on useful vase life, which was terminated at this point due to excessive leaf blackening. Water loss appears to have a minimal influence on 'Sylvia' protea leaf blackening. Shading at four and three weeks prior to harvest coincided with a period of significant flowerhead dry mass increase. It is thought that shading at this point, concurrent with an increased carbohydrate demand by the developing flower head resulted in a temporary limitation in carbohydrate supply resulting in the appearance of preharvest leaf blackening. It would appear that proteas do not store large quantities of carbohydrate. Although accentuating winter light conditions by shading did result in a decrease in carbohydrate content the fact that carbohydrate content was already low precluded shading from having a significant impact on postharvest leaf blackening. The finding that glucose was beneficial in extension of both storage and vase life of 'Sylvia' proteas directed research into its use for other Protea and Leucospermum cut flowers. Significant differences in the response to glucose supplementation were found in both Protea and Leucospermum (pincushions). The significant difference in sensitivity to glucose concentration in 'Pink Ice' proteas (phytotoxic at 2:4%) and 'Susara' proteas (no apparent toxicity), in conjunction with a lack of response in 'Cardinal' proteas, a hybrid from the same parents as 'Sylvia' indicates the need to direct future research to individual cultivars. Glucose supplementation had no beneficial effect on vase life of 'Scarlet Ribbon' and 'Tango' pincushions, whilst significantly extending vase life of 'Cordi', 'Gold Dust', 'High Gold' and 'Succession' pincushions. / AFRIKAANSE OPSOMMING: Blaarverswarting is 'n spesifieke probleem wat die vaasleeftyd en die bemarkbaarheid van Protea snyblomme beperk. In hierdie navorsing is ondersoek ingestel na die onderdrukking van Protea blaarverswarting met spesifieke fokus op die snyblomme van die kv. Sylvia (P. eximia x P. susannae). Die voorkoms van blaarverswarting by 'Sylvia' het merkbaar afgeneem tydens die verlaging van bergingstemperature. Hierdie afname is toegeskryf aan 'n laer respirasietempo en die behoud van koolhidrate. Lae bergingstemperature in die korttermyn hantering van die produk tydens lugvrag was voordelig. Die gebruik van lae temperature, slegs tydens die langer verskeepingsperiode, was egter onbevredigend vir vaasleeftyd verlenging en onderhoud van 'Sylvia' protea. Die afkoeling van 'Sylvia' proteas onder vakuum het blaarverswarting in 'n groot mate onderdruk en het beter resultate gelewer as geforseerde lugverkoeling. Alhoewel die verwydering van die heel boonste blare blaarverswarting by korttermynopberging vertraag het, het dit geen merkbare voordele vir langer bergingsperiodes ingehou nie. Ringelering direk onder die blomkop van die 'Sylvia' protea het blaarverswarting aansienlik verminder, en saam met lae bergingstemperature (O°C) het dit 'n merkbare verlenging in beide die bergingstyd en die vaasleeftyd van 'Sylvia' proteas teweeggebring. 'Sylvia' proteas het geen klimakteriese respirasiekruin tydens 'n bergingsperiode van 96 uur teen O°C getoon nie. Blootstelling aan etileen het nie die Protea blaarverswarting laat toeneem of 'n nadelige effek op die vaasleeftyd van die proteas of speldekussings wat geevalueer is, gehad nie. Geen voordelige reaksie op sukrose-byvoeging is in 'Sylvia' proteas gevind nie. 'n Analise van die suikerinhoud van beide die blomkoppe en die blare het aangetoon dat 'n glukose-byvoeging moontlik voordelig kon wees, en hierdie aspek is ondersoek. Met stooroplossings van 2,5 % glukose is die vaasleeftyd aansienlik verleng omdat daar 'n merkbare afname in blaarverswarting was. Vir die eerste keer in die geval van die 'Sylvia' protea, het die vaasleeftyd van die snyblomrne tot 'n einde gekom omdat die blornkoppe uitmekaar gebreek het en nie omdat blaarverswarting ingetree het nie. Die vaasleeftyd is aansienlik verleng met ~ 3% glukose-pulsoplossings, en blaarverswarting is merkbaar onderdruk met die verhoging van hierdie oplossings se glukosekonsentrasie. Die opname van die oplossings is gefasiliteer deur hoe intensiteit PAR (fotosinteties-aktiewe radiasie) ligte vroeg in die oggend, en is toegeskryf daaraan dat meer huidmondjies oopgegaan het. Dit het gelei tot 'n toename in transpirasie en 'n toename in die opname van die glukose-oplossing. Die feit dat glukose-oplossings vinniger opgeneem is deur lote wat in die middag geoes is, is toegeskryf daaraan dat loottemperature dan hoer is as soggens en gevolglik lei tot 'n vinniger transpirasietempo. Daar was 'n merkbare afname in die opnametyd wanneer die temperatuur van die pulsoplossings verhoog is. Vakuumafkoeling kon dus vroeer toegepas word, wat 'n verlenging in bergingstyd en vaasleeftyd tot gevolg gehad het. Verpakking van 'Sylvia' proteas in kartonne wat met poli-etileen uitgevoer is, het blaarverswarting van lote wat nie aan pulsering onderwerp is nie, onderdruk. Hierdie maatreel het egter geen praktiese waarde met betrekking tot vaasleeftyd nie; die vaasleeftyd het tot 'n einde gekom as gevolg van omvangryke blaarverswarting. Dit lyk asof waterverlies weinig invloed het op die blaarverswarting van' Sylvia' proteas. Die vermoede bestaan dat lae koolhidraatvlakke proteas ontvanklik maak vir blaarverswarting. Alhoewel die beklemtoning van winterligtoestande deur beskaduwing gelei het tot 'n afname in koolhidraatinhoud, was hierdie inhoud reeds laag en blaarverswarting na die oes is nie beinvloed nie. Beskaduwing tydens die vier en drie weke voor oestyd het saamgeval met 'n tydperk van aansienlike toename in die droe massa van die blomkop. Die vermoede bestaan dat beskaduwing tydens hierdie fase, saam met die toename in die ontwikkelende blomkop se behoefte aan koolhidrate, aanleiding gegee het tot 'n tydelike beperking in koolhidraatvoorraad wat die voorkoms van blaarverswarting voor die oes tot gevolg gehad het. Die bevinding dat glukose voordelig is vir die verlenging van beide die bergingstyd en die vaasleeftyd van 'Sylvia' proteas het die navorsing gerig om ook ondersoek in te stel na die gebruik daarvan vir ander Protea en Leucospermum snyblomme. Merkbare veranderinge is gevind in die reaksie op glukosebyvoegings in beide Protea en Leucospermum (speldekussings). Die opmerklike verskil in sensitiwiteit vir glukosekonsentrasie in 'Pink Ice' proteas (fitotoksies by ~ 4%) en 'Susara' proteas (geen klaarblyklike toksisiteit), saam met 'n gebrek aan reaksie by 'Cardinal' proteas, 'n hibried van dieselfde ouers as 'Sylvia', dui aan dat verdere navorsing op individuele kultivars toegespits sal rnoet word. Glukosebyvoegings het geen voordelige uitwerking op die vaasleeftyd van 'Scarlet Ribbon' en 'Tango' speldekussings gehad nie, terwyl dit die vaasleeftyd van 'Cordi', 'Gold Dust', 'High Gold' en 'Succession' speldekussingkultivars merkbaar verIeng het.

Thesis (MScAgric)--Stellenbosch University, 2003. / ENGLISH ABSTRACT: Protea cut flowers are exported worldwide but the vase life of some species and cultivars is considerably shortened by post-harvest leaf blackening. Research has established carbohydrate depletion to be positively correlated with this disorder. Consequently, a study had been made of the carbohydrate status of various species and cultivars, as well as the effect of supplemental glucose (pre and post-storage) on leaf blackening. Glucose, fructose, sucrose and starch concentrations of various Protea species and cultivars held in water were measured at harvest, and again at leaf blackening initiation. All measured carbohydrates declined significantly in 'Carnival', 'Pink Ice' and 'Sheila'. In 'Cardinal' all carbohydrate concentrations decreased significantly, except the sucrose concentration in the inflorescence. 'Susara' and 'Ivy' had very high initial carbohydrate concentrations in the leaves which decreased significantly. The very high initial carbohydrate concentrations in the inflorescence of 'Ivy' declined significantly. 'Brenda' differed from the other cultivars and species in that glucose concentrations increased over time. Carbohydrate concentrations of most of the tested proteas declined significantly from harvest to the initiation of leaf blackening. This highlighted the dependence of the leaves and inflorescence on the carbohydrate reserves, further substantiating the carbohydrate depletion theory. The inflorescences were characterized by high fructose and glucose concentrations and low sucrose concentrations when compared to the leaves. It was hypothesized that glucose pulsing and cold storage at 1°C for three weeks would significantly reduce leaf blackening. 'Brenda', 'Cardinal', 'Carnival', 'Pink Ice', 'Susara ' and 'Sylvia' had significantly less leaf blackening with glucose treatments of 4 and 10%. Leaf blackening of 'Sheila', P. cynaroides and P. grandiceps was not significantly reduced by glucose pulsing. P. magnifica showed a small, but significant, reduction in leaf blackening in response to the 3, 6 and 9% treatments after 10 days only, but despite this, leaf blackening was unacceptably high. 'Pink Ice' harvested at the soft tip stage had less leaf blackening than those harvested open or closed. Toxicity symptoms on the leaves, and in some instances flowers, were observed at higher glucose concentrations (8 and 10%) onP. grandiceps, P. cynaroides, 'Cardinal' and 'Sheila'. All glucose treatments resulted in toxicity symptoms on P. magnifica. A decrease in nonstructural carbohydrates post-harvest apparently occurs in all proteas but it appears that only members of the Ligulatae respond to glucose. Glucose pulsing followed by cold storage at 1°C for three weeks in combination with post-storage glucose vase solutions, significantly reduced leaf blackening of some Protea cultivars. Glucose (1 and 2%), with hypochlorite, significantly delayed leaf blackening in 'Cardinal' and 'Sylvia' after seven days. Leaf blackening of 'Brenda', 'Carnival', 'Pink Ice' and 'Susara' was not significantly reduced by the glucose vase solutions. Other disinfectants, in combination with the sugar treatments, need to be evaluated since the hypochlorite treatment had a dehydrating effect on all the cultivars and resulted in increased leaf blackening. Carbohydrate supplementation of protea flowers with glucose, pre and post-storage, will help meet the post-harvest carbohydrate requirements of certain Protea cultivars and species to an extent. Glucose treatments must be seen in conjunction with maintaining the cold chain and when combined with cold chain maintenance, can extend the storage and vase life. / AFRIKAANSE OPSOMMING: Protea snyblomme word wêreldwyd uitgevoer alhoewel die vaasleeftyd van sommige spesies en kultivars beduidend verkort word deur na-oes loof verbruining. Navorsing het koolhidraatverbruik positief gekorreleer met hierdie probleem. Gevolglik is 'n studie gemaak van die koolhidraatstatus van verskeie spesies en kultivars asook die effek van addisionele glukose (voor en na opberging) op loofverbruining. Glukose, fruktose, sukrose en stysel konsentrasies van verskeie Protea spesies en kultivars wat in water gehou is, is bepaal met oes en weer met die eerste tekens van loofverbruining. Al die gemete koolhidraatkonsentrasies het beduidend afgeneem in 'Carnival', 'Pink Ice' en 'Sheila'. In 'Cardinal' het al die koolhidraatkonsentrasies beduidend afgeneem, behalwe vir die sukrosekonsentrasie in die blom. 'Susara' en 'Ivy' het baie hoë begin koolhidraatkonsentrasies in die blare wat beduidend afneem. Die baie hoë inisiële koolhidraatkonsentrasies in die blom van 'Ivy' neem beduidend af met tyd. 'Brenda' verskil van die ander kultivars en spesies deurdat die glukosekonsentrasies toeneem met tyd. Koolhidraatkonsentrasies van die meeste getoetste proteas neem beduidend af vanaf oes totdat die eerste tekens van loofverbruining verskyn. Dit het die afhanklikheid van die blare en blom op die koolhidraatreserwes beklemtoon en daardeur verder die koolhidraatteorie ondersteun. Die blomme is gekarakteriseer deur hoë fruktose- en glukosekonsentrasies en lae sukrosekonsentrasies wanneer dit met die blare vergelyk is.Die hipotese is gestel dat die voorsiening van glukose, vir 'n aantal ure, gekombineerd met koue opberging by 1°C vir drie weke loofverbruining beduidend sal verminder. 'Brenda', 'Cardinal', 'Carnival', 'Pink lee', 'Susara' en 'Sylvia' het beduidend minder loofverbruining met glukose behandelings tussen 4 en 10%. Loofverbruining van 'Sheila', P. cynaroides en P. grandiceps is nie beduidend verminder deur glukose behandelings nie. P. magnifica het 'n klein, maar beduidende verlaging in loofverbruining getoon met die 3, 6 en 9% behandelings na 10 dae, maar ten spyte hiervan was loofverbruining onaanvaarbaar hoog. 'Pink lee' is geoes by die sagte punt stadium en het minder loofverbruining gehad as blomme wat oop of toe geoes is. Toksisiteitsimptome op die blare, en in sommige gevalle blomme, is waargeneem met hoër glukose konsentrasies (8 en 10%) op P. grandiceps, P. cynaroides, 'Cardinal' en 'Sheila'. Alle glukosebehandelings het toksisiteitsimptome tot gevolg gehad op P. magnifica. 'n Afname in nie-strukturele koolhidrate na oes kom waarskynlik voor in alle proteas maar dit wil voorkom of slegs lede van die Ligulatae positief reageer op glukose. Glukosebehandeling gevolg deur koue opberging by 1°C vir drie weke in kombinasie met na-stoor glukose vaasoplossings het loofverbruining van sommige Protea kultivars beduidend verminder. Glukose (l en 2%), saam met hipoehloriet, het loofverbruining beduidend verminder in 'Cardinal' en 'Sylvia' na sewe dae. Loofverbruining van 'Brenda', 'Carnival', 'Pink lee' en 'Susara' is nie beduidend verminder deur die glukose vaasoplossings nie. Ander ontsmettingsmiddels in kombinasie met die suikerbehandelings moet geëvalueer word aangesien die hipoehlorietbehandeling 'n dehidrerende effek op al die kultivars gehad het en 'n toename in loofverbruining tot gevolg gehad het. Byvoeging van glukose by proteablomme, voor en na opberging, sal tot 'n mate help om in die na-oes koolhidraatbehoeftes van sekere Protea kultivars en spesies te voorsien. Glukosebehandelings moet saam met die beheer van die koueketting gesien word en wanneer gekombineerd met koueketting beheer kan dit opberg en vaasleeftyd verleng.

South African ‘Eureka’ lemon fruit must be exposed to chilling temperatures (± 0.6°C) as a mandatory quarantine treatment against insect pests for all its overseas markets. Chilling lemon fruit at such temperatures may develop chilling injury (CI) symptoms on the flavedo. This negative effect on fruit quality reduces fruit marketability. This study evaluated postharvest factors influencing physiological, biochemical and ultra-structural mechanisms involved in alleviating CI in lemon fruit. It was hypothesised that treatment with methyl jasmonate (MJ) and salicylic acid (SA) may enhance chilling tolerance in lemon fruit by maintaining cellular integrity and inducing synthesis of enzymatic and non-enzymatic antioxidants. Furthermore, fruit susceptibility to CI was associated with the source of fruit. Lemon fruit were harvested from three locations representative of moderate subtropical, warm temperate and cool subtropical environments. Harvested fruit were treated either with 10 μM MJ, 2 mM SA or 10 μM MJ plus 2 mM SA, stored either at -0.5, 2 or 4.5°C for 0, 7, 14, 21, or 28 days and afterwards transferred to 23°C for a week as shelf-life simulation. Thereafter, fruit were evaluated for alterations in physiological, biochemical and ultra-structural features involved in the manifestation of CI symptoms. Chilling damage was more severe in untreated lemon fruit than in treated lemon fruit. Storing lemon fruit at 4.5°C accelerated the manifestation of CI symptoms more so than at 2°C while storage at -0.5°C delayed the manifestation of CI symptoms. Lemon fruit of moderate subtropical origin were more chilling-tolerant than lemon fruit of warm temperate and cool subtropical origin. Treatment with 10 μM MJ plus 2 mM SA significantly (P < 0.05) improved chilling tolerance in lemon fruit. This treatment effectively maintained membrane integrity, thereby retarding electrolyte leakage and membrane lipid peroxidation as well as mass loss and respiration rate. Treatment with 10 μM MJ plus 2 mM SA was also effective in enhancing the antioxidant concentrations of vitamin E and carotenoids. The production of these antioxidants could have been part of a defence system against chilling damage, reducing CI and maintaining fruit quality. Treatment with 10 μM MJ plus 2 mM SA enhanced the concentration of compounds involved in chilling resistance, such as proline, soluble sugars, ascorbic acid and total phenolics as well as the enzyme phenylalanine ammonia-lyase (PAL). The enhancement of the defence mechanisms may have played a role in enhancing chilling tolerance in lemon fruit. The treatment also inhibited certain enzymes involved in tissue browning, such as peroxidase (POD) which might have contributed to delaying manifestation of symptoms. Polyphenol oxidase (PPO) was found to not be a good biochemical marker of the occurrence of CI. Treatment with 10 μM MJ plus 2 mM SA appeared to be able to enhance chilling tolerance in lemon fruit by maintaining the ultra-structure of the cuticle, cell wall integrity, cell membrane of parenchyma cells of the flavedo. This treatment also preserved the mineral nutrients of the flavedo (carbon, oxygen, phosphorus, potassium, calcium, magnesium, sulphur, sodium, silicon and aluminium) during cold storage. This could have played a role in protecting the fruit against chilling stress and maintaining fruit quality. Treatment with 10 μM MJ plus 2 mM SA reduced ROS production, while the activity of enzymatic antioxidants such as catalyse (CAT), ascorbate peroxidase (APX) and glutathione reductase (GR), and accumulation of essential proteins was enhanced. This increase in activity of enzymatic antioxidants and the presence of stress-responsive proteins in the lemon flavedo could have been directly involved in enhancing chilling tolerance. The CI symptoms were accompanied by an increase in membrane permeability, membrane lipid peroxidation as well as phospholipase D (PLD) and lipoxygenase (LOX) activity; however, treatment with 10 μM MJ plus 2 mM SA effectively reduced the membrane permeability, membrane lipid peroxidation, and PLD and LOX activity induced by the cold treatment. This could have contributed to the efficacy of 10 μM MJ plus 2 mM SA in inhibiting the manifestation of CI symptoms. Treatment with 10 μM MJ plus 2 mM SA enhanced flavedo total antioxidant capacity measured by ferric reducing ability of plasma; 2,2-diphenyl-1-picrylhydrazyl; 2,2-azinobis (3-ethyl-benzothiazoline-6-sulfonic acid) and the oxygen radical absorption capacity assays. The enhancement of antioxidant capacity in lemon flavedo could have contributed to the fruit’s chilling tolerance. Therefore, the effect of 10 μM MJ plus 2 mM SA treatment, enhancing chilling tolerance, may be attributed to its ability to enhance enzymatic and non-enzymatic antioxidants; activate essential proteins and mitigate the effect of ROS accumulation. With the use of 10 μM MJ plus 2 mM SA treatments, the South African citrus industry will be able to meet the quarantine temperature requirements for exportation of lemon fruit whilst reducing economic losses, depending on the preharvest conditions experienced by the fruit in each shipment. / Thesis (Ph.D.)-University of KwaZulu-Natal, Pietermaritzburg, 2013.