ABSTRACT. This study examined biochemical changes associated with chilling injury (CI) in sweet potato roots stored at low temperatures and reconditioned at ambient temperature. Sweet potato cultivars BRS Amélia and BRS Rubissol were stored at 6 or 13°C for 4 days at ambient temperature (“ambient reconditioning”: 21 ± 2°C). CI on the outer surface of the roots occurred earlier in BRS Amélia than in BRS Rubissol. The CI index on the inner surface of the BRS Amélia was higher when it was stored at 6°C for 40 + 4 days. BRS Amélia showed higher proline content and electrolyte leakage when stored at 6°C. Ascorbate peroxidase was induced by storage at 6°C for 30 + 4 days in BRS Amélia and from 40 + 4 days in BRS Rubissol. The malondialdehyde and phenolic compounds of BRS Rubissol increased during storage at 6°C. CI in both cultivars was associated with increased peroxidase and polyphenol oxidase activities. Storage of sweet potato cultivars at 6°C for 50 + 4 days caused severe damage to the roots. Cultivars BRS Amélia and BRS Rubissol showed similar symptoms of CI and can be characterized as being sensitive to low temperatures.

Resumo A longevidade das flores de corte é limitada por sua natureza efêmera e por diversos estresses. De forma geral, a diminuição da absorção de água, esgotamento dos carboidratos armazenados, aumento da atividade respiratória e produção de etileno são reflexos senescência floral. Uma ampla gama de técnicas está disponível para estender a preservação de flores, incluindo o uso de conservantes de flores, inibidores da ação do etileno, reguladores de crescimento e controle de temperatura e desidratação das flores. O uso de sacarose em solução pulsante ou como constituinte de solução de vaso pode estender a vida de vaso das flores, melhorando o balanço hídrico, estimulando a abertura das flores ou retardando a senescência devido à menor síntese de etileno. Os inibidores da produção e ação do etileno afetam a longevidade, estendendo a vida de vaso de algumas flores sensíveis ao etileno. As flores têm intensa atividade respiratória, o que pode esgotar as reservas limitadas de carboidratos armazenados nas hastes cortadas. A redução da temperatura reduz tremendamente a produção de CO2 e etileno, bem como a sua ação. No entanto, em flores sensíveis ao frio como ave-do-paraíso, helicônia, orquídea e gengibre não podem ser armazenadas abaixo de 10 a 13ºC devido ao intenso desenvolvimento de descoloração do tecido.

Abstract The longevity of cut flowers is limited by their ephemeral nature and by multiple stresses. Impairment in water uptake, depletion of stored carbohydrates, increases in both respiratory activity and ethylene production are signatures of flower senescence. A wide range of techniques is available to extend flower preservation, including the use of flower preservative solutions, ethylene action inhibitors, growth regulators, and control of temperature and flower dehydration. The use of sucrose in pulsing solution, or as a component of vase solution, extends the vase life of flowers by either improving water balance and energy or delaying the senescence via reductions in ethylene biosynthesis. Inhibitors of ethylene production and action affect the longevity by extending the vase life of some ethylene-sensitive flowers. Flowers have intense respiratory activity, which may deplete the limited reserves of carbohydrates in the tissues. Lower temperatures markedly reduce both carbon dioxide concentration and ethylene production as well as its action. However, chilling-sensitive flowers, such as bird-of-paradise, heliconia, orchid, and ginger, cannot be stored below 10 to 13°C due to the intense development of tissue discoloration.

Abstract One of the major problems affecting potatoes quality on stored is the susceptibility to enzymatic browning, which occurs mainly after wounds during the harvest, at postharvest handling and by aging, leading to the development of dark color compounds. Enzymatic browning is associated with the action of polyphenoloxidases (PPO) and peroxidases (POD), which use phenolic compounds and oxygen as substrates. The products of these enzymes cause undesirable changes of color and flavor of processed potato products. The present study aimed to evaluate some kinetic properties based to optimum pH and reaction temperature, and to determine changes on activity of potato tubers PPO and POD treated with sprouting suppressors compounds menthol and eugenol. For each treatment, samples were collected in six different periods, before application (day 0) and 10, 20, 30, 40, and 50 days after the treatments to determine the influence of sprout inhibitors on the activity of PPO and POD. Changes in pH and temperature affected drastically the activity of both enzymes. The use of eugenol and menthol as sprouting suppressors decreased enzymatic activity on the treated tubers compared to control with an inverse relationship between enzymes activity and content of phenolic compounds.

ABSTRACT. The increased demand for potato by the Brazilian processing industry requires long term refrigerated storage, but after a few months, natural dormancy ends, and sprouts start to grow. Thus, sprout inhibitors are necessary to reduce the rate of growth and allow further storage. The purpose of research described here was to determine the effects clove and menthol essential oils have on the inhibition of sprout growth in non-dormant ‘Asterix’ tubers. Both eugenol and menthol treatments reduced the rate of sprout growth during storage at 8oC for up to 50 days. Eugenol and menthol essential oils diminished the rate of accumulation of reducing sugar, which are responsible for browning of French fries. Color after frying was within acceptable levels when the tubers were treated with eugenol or menthol essential oils.

ABSTRACT The breakdown of dormancy and early sprouting is one of the main causes of losses of stored potatoes. Sprouting control becomes important especially when tubers are submitted to long-term storage for further processing by the potato industry. The objective of this work is to evaluate the effect of organic sprout inhibitors, eugenol and menthol essential oils, on the suppression of growth on non-dormant ‘Asterix’ tubers stored at 8 °C. Administration of eugenol and menthol essential oils reduced the number and the length of sprouts during cold storage up to fifty days. Nevertheless, the essential oils stimulated the break of bud apical dominance, stimulating auxiliary buds growth. The effect of the oils was restricted to inducing necrosis of superficial sprout cells without any apparent effect on the skin periderm structure. Repeated applications of oils are necessary to prolong the inhibitory effects of the essential oils on sprouts growth.

ABSTRACT The gladiolus flower is classified as insensitive to ethylene. Thus, the signals that initiate senescence are poorly understood. This study evaluated the role of abscisic and gibberellic acids on postharvest senescence of 3 cultivars of cut gladiolus flowers (Gladiolus grandiflora Hort.). Stalks were harvested and placed in test tube containing 100 mL distilled water or an aqueous solution of abscisic acid (100 and 150 µM ABA), gibberellic acid (100 µM GA3), and fluridone (1 mM) for 24 h. Subsequently, flower stalks were placed in a test tube with distilled water, and the following variables were determined: stem longevity, fresh weight change, water uptake rate and transpiration rate during the vase life, as well as membrane stability index and lipid peroxidation in 5 stages of flower development. In another experiment, the florets were removed by cutting down the pedicel. After removal, florets were placed in a beaker containing 10 mL distilled water or the following solutions: 100 or 150 µM ABA; 100 µM GA3; 1 mM fluridone; and 100 µM ABA + 100 µM GA3, followed by immersion in distilled water after 24 h in each treatment. Fresh weight change and transpiration rate of florets were assessed every 24 h. Abscisic acid is involved in the induction of senescence-related events in gladiolus flowers, such as high loss of membrane stability and abnormal flower opening. GA3 regulates the action of ABA in the maintenance of cell membrane and opening of gladiolus flowers.