Storage conditions and ripening of the custard apple Annona squamosa L.

Annona squamosa is a climateric fruit in which maximal carbon dioxide production preceeds that of ethylene during post-harvest storage. Normal ripening occurred at temperatures between 15 and 30° C, although the fruits were susceptible to fungal attack at temperatures above 25° C. Storage temperatures below 15° C caused chilling-injuries. Ripening was enhanced by removal of carbon dioxide and by addition of oxygen to the storage atmosphere, and delayed by the addition of carbon dioxide or removal of oxygen. Ethylene had no apparent effect on ripening. Fruits maintained under low relative humidities ripened faster than those stored under high-humidity conditions. Dipping the fruits in a solution of indole acetic acid at concentrations between 10^?4 and 10^?2 M accelerated ripening. Levels of both ascorbic acid and glucose increased to a maximum at the climacteric, but decreased as the fruits became over ripe. The stage of “eating” ripeness occurred at the climacteric. Recommended conditions for storing custard apple are: temperatures between 15 and 20° C, low oxygen and ethylene tensions coupled with 10% carbon dioxide and a relative humidity of 85%–90% in the storage atmosphere.     

Modified atmosphere packaging of ‘Kolikuttu’ bananas at low temperature

Summary

Mature `Kolikuttu' bananas were packed under modified atmosphere (M.A.) conditions using low density polyethylene (LDPE) bags and stored at 14°C and 94% r.h. The effect of ethylene scavengers on storage life of banana was examined. The in-package concentrations of oxygen, carbon dioxide and ethylene were measured during storage. Percentage weight loss, changes in firmness, total soluble solids (TSS), pH and sugar: acid during storage were also determined. Based on the in-package gaseous composition, the optimum storage period was defined. After termination of storage, bananas were allowed to ripen naturally, and the physico-chemical properties of ripened banana were analysed. `Kolikuttu' bananas could be packed in LDPE (0.075 mm) and stored at 14°C and 94% r.h. for 24.d. Storage life could be further extended up to 30.d by using ethylene scavengers. Physico-chemical properties of M.A. stored banana after ripening were similar to those held under ambient conditions. Therefore, packaging of `Kolikuttu' banana as individual hands in LDPE (0.075.mm) bags of 1:1 surface to weight ratio (cm² g^-1) with 50 ml of saturated potassium permanganate absorbed onto suitable porous matrices could be recommended to increase storage lifeat 14°C.     

Sensitivity of Geraldton waxflower to ethylene-induced flower abscission is reduced at low temperature

Summary

Exposure to ethylene gas elicits flower abscission from cut stems of Geraldton waxflower (Chamelaucium uncinatum Schauer). Ethylene response rates in plants are mediated by temperature. At 20°C, flower abscission from waxflower ‘Purple Pride’ occurred upon 12 h exposure to 1 µ11^–1 ethylene. This ethylene treatment did not cause flower abscission at either 10 or 2°C. Moreover, flowers held at 2°C were insensitive to 48 h exposure to 1, 10 and 100 µ11^–1 ethylene. However, increasing the duration of treatment with 1 µ11^–1 ethylene at 10 and 2°C to 48 and 144 h, respectively, induced flower abscission. When flowers were held at 20°C in air without exogenous ethylene following continuous exposure to 1 µ11^–1 ethylene at 2°C, the duration required to elicit flower abscission was reduced from 144 to 72 h. Collectively, these responses show that maintaining harvested waxflower at low temperature (e.g. 2°C) is an effective means to minimise ethylene-mediated flower abscission.     

Effects of temperature and plant growth regulators on anthocyanin synthesis and phenylalanine ammonia-lyase activity in chicory (Cichorium intybus L.)

Summary

This study addresses the effects of air temperature and plant growth regulators on anthocyanin synthesis, sugar content and phenylalanine ammonia-lyase (PAL) activity in chicory (Cichorium intybus L.). Anthocyanin in chicory was synthesised at the highest level under 15°/10°C (day/night) temperatures, followed by 20°/15°C, and 25°/20°C; while synthesis was inhibited > 90% at 30°/25°C, resulting in an almost green colour. Sugar contents paralleled anthocyanin development under the same temperatures. The plant growth regulators, abscisic acid (ABA), ethephon and uniconazole all stimulated anthocyanin synthesis, with uniconazole treatment showing the greatest effect. Gibberellic acid (GA₃) inhibited anthocyanin development, while GA₃ in combination with uniconazole alleviated this inhibition.

PAL activity was higher at 15°/10°C or 20°/15°C (day/night) temperatures when plants were treated with ABA, ethephon or GA₃, than at 25°/20°C and 30°/25°C (day/night) temperatures. These results suggest that, under lower temperatures, plant growth regulators may play an important role in anthocyanin synthesis and PAL activity in chicory.     

Temperature requirements for the germination of olive seeds (Olea europaea L.)

Summary

Olive seeds cv Chondrolia Chalkidikis were subjected to temperatures of 5°, 10°, 15°, 20°, 25° and 30°C for one, two or three months, and were then transferred to 20°C. Exposure to 10° and 15° for one month or more caused higher emergence percentages compared to that at a constant 20°C. The highest germination rate was observed when seeds subjected to 10°C for one month were then transferred to 20°C. Seeds at 5°, 25° and 30°C did not germinate while being held to these temperatures; even when transferred to 20°C the percentage and rate of emergence were lower than those of seeds held at constant 20°C. In another experiment, in which seeds were subjected to 10°C for 0, 2, 4, 6 and 8 weeks before being transferred to 20°C, it was found that four weeks exposure to 10°C was near optimal. Emergence percentages of seeds at constant 10°C or at diurnally alternating temperatures of 10° for 16 h/20° for 8 h were high and equal (92%), but emergence in the latter treatment was slower. Alternating 10° with 25°C resulted in a 95% reduction of the emergence percentage. Transferring seeds immediately after chilling at 10°C for three or four weeks to 25°C, partially reversed the effect of the low temperature. However, the chilling effect could not be reversed when the seeds were subjected to 10°C for five weeks.     

Environmental interaction between day length,night temperature,and photon flux density on growth and flowering in Boronia megastigma Nees.

Summary

Boronia plants were placed in a range of environmental conditions, two night temperatures (6 and 15°C), three photon flux densities (full sunlight, 50% and 30%), and two day lengths (natural autumn to winter cycle and natural autumn to winter cycle plus synthetic to 16 h total light). Flowering occurred to some extent under all conditions; generally conditions suitable for high growth rates were not optimum for flowering, maximum numbers of flowers were achieved with low night temperatures (6°C), short days (10 h), and full to 50% sunlight. Floral development was influenced by all treatments.     

Effects of high-humidity storage on quality,decay and storage life of cherry,lemon and peach fruits

Sweet cherries (Prunus avium (L.) ‘Lambert’ and ‘Blackboy’), lemons (Citrus limon (L.) Burm. f. ‘Lisbon’) and peaches (Prunus persica (L.) Batsch, ‘Summerset’) were stored at 77–83, 90–94 and 95–99% RH (high humidity) at near-optimal storage temperatures after harvest and treatment with fungicides. High-humidity storage did not increase the storage life of peaches held at 0°C, but the life expectancy of cherries (both cultivars) was extended by 7–10 days at 0°C, and of lemons by at least 4 weeks at 10°C when fruit were stored at 95–99% RH compared with levels below 95%. The beneficial effects of high humidity were attributed to retardation of peel desiccation and associated reductions in fruit deformation, peel de-greening, chilling-injury and decay in lemons and to the maintenance of a fresher stalk and a firmer, less shrivelled fruit in cherries. High humidity had no effect on decay in cherries or peaches, but it significantly reduced weight loss and delayed the appearance of shrivel in peaches stored at 0°C. However, after storage at high humidity for 4 weeks, peaches ripened with low rates of C₂H₄ evolution and showed severe low-temperature injury, slight peeling-injury and a poor flavour ex-store.     

Effect of temperature on pollen germination and pollen tube growth of four cultivars of mango (Mangifera indica L.)

Summary

The effect of a constant (10, 15, 20 or 25°C) or a diurnal maximum/minimum (15/5, 20/10, 25/15 or 30/20°C) incubation temperature on in vitro pollen germination and pollen tube growth in the pistils of two poly-embryonic (‘Kensington’ and ‘Nam Dok Mai’), and two mono-embryonic (‘Irwin’ and ‘Sensation’) mango cultivars was studied. In in vitro experiments where pollen was incubated in a liquid germination medium for 24 h in darkness, little difference was found between pollen germination of mono- and poly-embryonic cultivars. Averaged over the four cultivars, 53.9% of pollen germinated at 10°C, this increased to 76.2% when the incubation temperature was increased to 15°C, thereafter up to 25°C the percentage germination remained stable but germination decreased slightly to 68.2% at 30°C. Similarly, there was no difference in percent germination between cultivars when pollen was incubated under diurnal temperature regimes. Mean pollen germination of all four cultivars was 52.3% at 15/5°C and pollen germination increased by 10% when the temperature was raised to 30/20°C. When self-pollinated flowers were incubated for 24 h on a semi-solid agar medium at 10°C, pollen tube growth of the four cultivars was retarded and no pollen tubes reached the ovaries. As the temperature was increased from 15 to 25°C, the mean number of pollen tubes in ovaries increased from 0.04 to 0.25. At 30°C, the mean number of pollen tubes that entered ovaries decreased to 0.04. After incubation under diurnal temperature regimes, the mean number of pollen tubes in ovaries of all four cultivars at 15/5°C was 0.23 and increased to 0.42 when the temperature increased to 30/20°C. At each incubation temperature, there were significant differences in pollen tube growth between cultivars, but there were no differences between the temperature response of pollen from mono- and poly-embryonic cultivars.     

The ripening of gamma irradiated fruits of jujube

Mature green jujube fruits of cv. Zaytoni were subjected to gamma radiation doses of 0, 10, 30 and 50 krad. The irradiated and unirradiated fruits were then kept at 20°C and 85-90% r.h., and changes in weight loss, total soluble solids, titratable acidity and ascorbic acid content were determined. Fruits subjected to 30 krad were firmer and greener than unirradiated control fruits after six days of storage, and this treatment delayed ripening by three days. There was no significant loss in the nutritive value of the fruit due to irradiation.     

Use of nitric oxide to reduce postharvest water loss from horticultural produce

Summary

Eleven types of fruit and vegetables and five types of flowers were held in an atmosphere containing a range of concentrations of nitric oxide (NO) gas in nitrogen for 2 h then stored for 24 h in air at 20°C and 60% r.h. Each type of produce was weighed before treatment, and after 24 h, and the rate of water loss calculated. Treatment with NO was found to result in 20% less water loss than in produce stored in air.     

Floral induction in tropical fruit trees: Effects of temperature and water supply

Summary

Floral induction in tropical trees generally follows a check in vegetative growth. However, it is not easy to identify the environmental factors involved in flowering, which normally occurs during the dry season when temperatures are also often lower. The separate and combined effects of temperature and water supply on floral induction were investigated in ‘Hass’ avocado (Persea americana), ‘Lisbon’ lemon (Citrus limon). ‘Wai Chee’ litchi (Litchi chinensis) and ‘Sensation’ mango (Mangifera indica). Low temperatures (15°/10°C or 15°/10°C and 20°/15°C compared with 30°/25°C and 25°/20°C) generally decreased vegetative growth and induced flowering in well-watered avocado, litchi and mango. A pre-dawn leaf water potential (ψ_L) of ?1.7 to ?3.5 MPa compared with ?0.4 to ?0.7 MPa in control avocado and litchi, and a pre-dawn relative water content (R.W.C.) of 90-93% compared with 97% or above in control mango plants also reduced or eliminated vegetative growth, but did not induce flowering. Low temperatures (15°/10°C compared with 20°/5°C, 25°/20°C or 30°/25°C) and water stress (pre-dawn ψ_L of ?2.0 to ?3.5 MPa compared with ?0.7 to ?0.8 MPa in controls) reduced or eliminated vegetative growth in lemon. In contrast to the response in avocado, litchi and mango, flowering in lemon was very weak in the absence of water stress at 15°/10°C or outdoors in Brisbane in subtropical Australia (Lat. 28°S), and was greatest after a period of water stress. The number of flowers increased with the severity and duration of water stress (two, four or eight weeks) and was generally greater after constant rather than with cyclic water stress. In lemon and litchi, net photosynthesis declined with increasing water stress reaching zero with a midday ψ_L of ?3.5 to ?4.0 MPa. This decline in carbon assimilation appeared to be almost entirely due to stomatal closure. Despite the reduction in midday CO₂ assimilation, starch concentration increased during water stress, especially in the branches, trunk and roots of lemon. Leaf starch was uniformly low. The number of flowers per tree in lemon was strongly correlated with starch in the branches (r²=77%, P<0.01) and roots (r²=74%, P<0.001). In litchi, starch was lower than in lemon roots and was not related to flowering.

In separate experiments to test the interaction between temperature and water supply, low day/night temperatures (23°/18° and 18°/15°C compared with 29°/25°C) reduced vegetative growth and induced flowering in avocado, litchi and mango. None of these species flowered at 29°/25°C or as a result of water stress (ψ_L of ?1.5 MPa compared with ?0.3 MPa for avocado and ?2.0 MPa compared with ?0.5 MPa for litchi, and R.W.C, of 90-93% compared with 95-96% in mango). In contrast, in lemon, flowering was very weak (<10 flowers per tree) in the absence of water stress (pre-dawn ψ_L of ?2.0 MPa compared with ?0.5 MPa) and was only heavy (>35 flowers per tree) after stressed trees were rewatered. There were slightly more flowers at 18°/15°C than at 23°/18° and 29°/25°C in control plants, but no effect of temperature in stressed plants. Starch concentration in the roots of avocado, lemon, litchi and mango was generally higher at 18°/15°C and 23°/18°C than at 29°/25°C. Water stress increased the starch concentration in the roots of lemon and litchi and decreased it in avocado. There was no effect in mango. There was a weak relation (r²=57%, P<0.05) between the number of flowers per tree in lemon and the concentration of starch in the roots. In contrast, there was no significant relationship between flowering and starch levels under the various temperature and water regimes in the other species. In another experiment, only vegetative growth in litchi and mango occurred at 30°/25°C and only flowering at 15°/10°C. Six weeks of water stress (pre-dawn ψ_L of ?2.5 MPa compared with ?1.0 MPa or higher in litchi, and R.W.C, of 90-93% compared with 95% or higher in mango) in a heated glasshouse (30°C days/20°C night minimum) before these temperature treatments did not induce flowering.

Temperatures below 25°C for avocado and below 20°C for litchi and mango are essential for flowering and cannot be replaced by water stress. The control of flowering in lemon over the range of day temperatures from 18°C to 30°C differed from that of the other species in being mainly determined by water stress. Flowering was generally weak in well-watered plants even with days at 18°C. Starch did not appear to control flowering.     

Use of low-pressure storage to improve the quality of tomatoes

Freshly harvested vine-ripened tomatoes (Solanum lycopersicum cv. Neang Pich) were stored at low pressure (4 kPa) at 10°C for 11 days with 100% RH. Fruit quality was examined upon removal and after being transferred to normal atmosphere (101 kPa) at 20°C for 3 days. Weight loss was significantly lower in fruits which were stored at low pressure (4 kPa) than in fruits that were stored at regular atmosphere (101 kPa) at 10°C. Fruits that were stored at low pressure (4 kPa) reduced calyx browning by 12.5%, and calyx rots by 16%, compared to fruits that were stored at regular atmosphere (101 kPa) at 10°C. Fruit firmness was not significantly different between fruits stored at low pressures (4 kPa) and the normal atmosphere (101 kPa), with an average firmness of 14 N after fruits were stored at 10°C for 11 days. There was no difference in the SSC/TA ratio. The results suggest that a low pressure of 4 kPa at 10°C has potential as an alternative, non-chemical postharvest treatment to improve tomato quality during storage.     

Leatheriness and mealiness of peaches in relation to fruit maturity and storage temperature

Summary

`Huangjin' peaches (Prunus persica Batsch) were harvested at commercial harvest time (commercial) and 20 d before (early) or after (later) commercial harvest. Fruit from each harvest were stored at three temperature regimes (0, 5 and 10°C) at 95% r.h. After four weeks of storage at 0 or 5°C, early harvested fruit developed more leatheriness but less mealiness and later harvested fruit did not develop leatheriness but developed more mealiness comparedwith fruit from commercial harvest. Overall, fruit stored at 5°C developed more mealiness but less leatheriness than fruitat 0°C for the same period of storage. When stored at 10°C for two weeks, after which fruit were senescent, fruit did not develop any leatheriness or mealiness regardless of harvest times. Fruit with leatheriness were firmer (>30 N) thanjuicy or mealy fruit (<10 N) after the same period of cold storage and 4 d at 20°C. Mealy fruit were as soft as juicy fruit. 1-Aminocyclopropane-1-carboxylate oxidase (ACO) activity, 1-aminocyclopropane-1-carboxylic acid (ACC) content, and polygalacturonase (PG) and galactosidase (GAL) activities were lower, and insoluble pectin content was higher in leathery fruit than that in juicy or mealy fruit. ACO, PG and GAL activity, ACC, and insoluble pectin content were similar between mealy and juicy fruit.     

Effect of temperature on growth,dry matter production and starch accumulation in ten mango (Mangifera indica L.) cultivars

Summary

Ten mango cultivars of tropical and subtropical origin (Carabao, Kensington, Nam Dok Mai, Alphonso, Dashehari, Florigon, Glenn, Irwin, Haden and Sensation) were grafted onto cv. Kensington seedling rootstock and held at four day/night temperatures for 20 weeks (15/10°C, 20/15°C, 25/20°C and 30/25°C). Vegetative growth increased with increasing temperatures. All grew vegetatively at 25/20°C and 30/25°C. Cultivars which did not grow at 20/15°C were Carabao, Kensington and Dashehari. Cultivars Kensington, Nam Dok Mai, Alphonso, Florigon, Glenn, Irwin, Haden and Sensation produced flower panicles at 15/10°C. The rise in temperature increased the average number of growth flushes (in responsive cultivars) from 0.48 at 15/10°C to 3.21 at 30/25°C, and the number of leaves per growth flush (1.22 at 15/10°C to 13.63 at 30/25°C). Distribution of dry matter from new growth was mostly to the roots at the lowest temperature (95% at 15/10°C) and to the leaves (58%) at 30/25°C. The mean daily temperature for zero vegetative growth was calculated to be 15°C. Temperature and related growth activity also affected the concentration of starch in the woody tissue of rootstock trunks at the end of 20 weeks (15.9% starch at 15/10°C v. 4.8% starch at 30/25°C). ‘Irwin’ had the highest starch concentration at the two higher temperatures (twice that of any other cultivar at 30/25°C) while ‘Kensington’ the lowest starch level at 25/20°C, ca. 50% of most other cultivars.     

Effects of post-harvest storage conditions on the levels of glucosinolates in broccoli sprouts (Brassica oleracea var. italica) grown under different temperature regimes

Summary

Broccoli sprouts have been recognised as a rich source of glucosinolates, particularly 4-methylsulphinylbutyl glucosinolate, the precursor of the potent anti-cancer compound, sulphoraphane. Previous results have shown that temperature can significantly affect the levels of glucosinolates. In this study, we showed how sprout age and storage temperature affected glucosinolate levels in broccoli sprouts grown under different temperature regimes. Experiments were conducted in growth cabinets with day/night temperature regimes of 30°/15°C, 22°/15°C and 18°/12°C. At 9, 10 and 11 d after sowing in the first temperature regime, 10, 11 and 12 d in the second, and 12, 13 and 14 in the third, sprouts were submitted to 4°C or 20°C to simulate refrigerated and room temperature storage. Sampling was done after 1 d or 2 d of exposure to these conditions. The results showed that total glucosinolate levels and the potential health effects of broccoli sprouts depended on the growth temperature regime (P < 0.05), the age of the sprouts (P < 0.001), and the storage conditions (P < 0.01). The highest total glucosinolate levels (65.7 µmoles g^–1 dry weight) were obtained under the 30º/15°C temperature regime for the youngest sprouts (harvested 9 d after emergence), after being submitted to a storage temperature of 4°C for 24 h. However, these levels were much lower than in 3-d-old sprouts. Consuming old sprouts provides less health-protective effects due to reduced levels of glucosinolates.     

The effect of temperature on certain chemical changes and the storage behaviour of jujube fruits (Zizyphus spinachristi (L.), Willd.)

Summary

Jujube fruits (Zizyphus spinachristi (L.) Willd.) cv. Bambawi were harvested at the mature green stage and stored at 10°C and 27–30°C. Titratable acidity and total chlorophyll decreased as the fruit matured, the rate of decline being more rapid at the higher temperature. Total soluble solids, carotenoids and ascorbic acid contents of the fruit increased towards maturity, the increase being faster at the higher temperature. Jujube fruits could be stored for six days at room temperature and twenty-five days under refrigeration at 10°C.     

Optimization of agrotechniques in the cultivation of Luffa acutangula

Germination requirements, flowering pattern, planting density and growing regimes were examined for Luffa acutangula (L.) Roxb. Maximum germination (50%) was obtained at 35°C, and at 8, 12, and 45°C germination was completely inhibited. Partial removal of the seed coat increased the percentage of germination while vernalization and exposure to salinity 5=50 mM NaCl reduced it. Planting season influenced flowering pattern, with significantly more female flowers being produced in spring-summer (long days and high temperatures) than in autumn-winter (short days and low temperatures). A high yield of 44.5-47.3 Mg ha 1 was obtained for plants trained on trellises at planting densities of 10,000 and 20,000 plants ha-1. Fruits kept at low temperatures showed the least deterioration during storage, a shelf life of about two weeks being demonstrated at 4°C.     

Investigation of Antioxidant Content and Capacity in Yellow European Plums

ABSTRACT

Phenolic content and antioxidant capacity of five Yellow European plums (Prunus domestica) were studied using heat reflux extraction. Fresh plums were extracted at 50°C and 70°C, while freeze dried plums were extracted at 50°C, 60°C, and 70°C. Quantification of phenolic compounds such as ascorbic acid, neochlorogenic acid, and chlorogenic acid, was performed using high performance liquid chromatography. Antioxidant activity was determined by evaluating the scavenging ability of 2,2-diphenyl-1-picrylhydrazyl (DPPH) and ferric (Fe³⁺) free radicals. Total phenolic content and ferric reducing antioxidant potential were highest for freeze dried samples extracted at 60°C whereas extraction at 70°C resulted in the lowest yield. Neochlorogenic acid was the predominant phenolic compound in each plum genotype followed by ascorbic acid and chlorogenic acid. This study demonstrates that there is an adequate amount of health promoting phytochemicals within European plums, hence extraction of these compounds have potential for use towards functional food, nutraceutical, and pharmaceutical industries.     

Corm induction and multiplication of Amorphophallus albus in vitro

Summary

Amorphophallus albus, belonging to the family Araceae, has attracted widespread attention due to its considerable economic and medicinal importance. The natural propagation coefficient of A. albus is very low, which limits application of this crop. In vitro corms can be used for propagation of A. albus and have been proved to be superior over in vitro plantlets. To optimise procedures for in vitro corm production and multiplication, the effects of phytohormones, sucrose concentrations and incubation conditions with desirable phytohormone combinations for callus induction, corm formation and corm growth of A. albus were investigated. The results showed that calli were induced at high frequency from petiole segments on Murashige and Skoog medium supplemented with 1.0 mg l^–1 naphthaleneacetic acid (NAA) and 1.0 mg l^–1 6-benzyladenine (BA). Compact nodular calli were desirable for corm formation, and optimum corm formation was obtained in the presence of 0.5 mg l^–1 NAA and 2.0 mg l^–1 BA. With this auxin and cytokinin combination, an increase in sucrose concentration from 2% to 6% (w/v) significantly increased the corm formation rate and favoured corm growth, but negative effects occurred at higher sucrose concentrations. By incubating over a range of temperatures from 19°C – 28°C, 22°C produced the largest numbers of corms and highest mean fresh weight of each corm. Short-day (8 h) or long-day (16 h) photoperiods did not affect corm formation and growth significantly, except that corm weight fell under long-day conditions. The multiplication rate of in vitro corms was enhanced by apical meristem wounding. It was possible to store in vitro produced corms at 4°C for as long as 90 d to overcome apical dormancy and accelerate sprouting after planting into soil. This work has established an efficient protocol for multiplication of A. albus through an in vitro corm system.