Quality of lemons sealed in high-density polyethylene film during long-term storage at different temperatures with intermittent warming

Storage of lemons is designed to extend the marketing of fruit throughout the year, from the main harvest season in the winter until late summer, which is a period of short supply in the market. This work was concerned with physiological and chemical attributes of stored lemons either seal-packaged in high-density polyethylene plastic film (HDPE), or left unwrapped, during storage at 13, 8 and 2°C. Intermittent warming (IW) was used to prevent chilling injury at the lower temperatures. Differences between fruit subjected to the two treatments which produced longest storage (sealed at 13°C and non-sealed at 2°C with IW) are discussed. Both treatments are recommended for adoption in commercial practice.     

Effect of intermittent warming on the reduction of chilling injury of Villa Franka lemon fruits stored at cold temperature

Storing lemon fruits at temperatures below 13°C caused chilling injury, namely physiological and chemical disorders and the development of excessive rot. However, warming the fruit for 7 days at 13°C after every 21 days in cold storage prevented chilling injury and enabled lemons to be kept in storage for six months and longer and retain marketable quality.     

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.     

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.     

Reduction of chilling injury in ‘Tommy Atkins’ mangoes during ripening

Studies were conducted to investigate how harvest maturity influence fruit ripening processes to alleviate chilling injury (CI) in mangoes (cv. Tommy Atkins). Fruit at three stages of maturity, immature (M1), half-mature (M2) and mature (M3) were stored for 18 days at 5 °C and then at 1 or 3 days at 20 °C. M1 fruit succumbed to CI after 18 days at 5 °C, with symptoms increasing in severity upon warming. Low C₂H₄ production, poor colour development, minor changes to fruit composition, insipid flavour and poor aroma revealed that fruit ripening was insufficient to reduce CI compared to M2 and M3 fruits. M2 and M3 fruits had higher C₂H₄ production rates than M1 fruit and ripened normally with acceptable flavour and aroma after 18 days at 5 °C and 3 days at 20 °C. While M3 fruit had no CI symptoms, they were overripe and fruit decay incidence was 26.6%, compared to M2 fruit which had no decay, a trace of CI symptoms and possessed the best overall quality.     

Peroxidase activity in avocado fruit stored at chilling temperatures

No increase in peroxidase activity was observed in ‘Fuerte’ avocado fruits which showed chilling injury symptoms as a result of storage at 0 or 2°C. Peroxidase activity in the fruit declined along with fruit softening during the ripening process. It is suggested that peroxidase acitivity in avocado fruit mesocarp has no role in the development of the chilling injury disorder appearing as dark patches on the skin of the fruit.     

黄瓜果实不同部位的耐冷性差异

 为了研究黄瓜果实采后的耐冷性,'津优1号'黄瓜（Cucumis sativus L.）果实在2 ℃下贮藏9 d后,转移到20 ℃下放置2 d,分别测定果脐（靠近花萼）、中部、果肩（靠近果梗）三个部位的冷害指数、电导率、磷脂酶D（PLD）和脂氧合酶（LOX）活性、膜结合Ca2+含量。黄瓜果实的冷害最初在脐部出现,再逐渐漫延到中部和肩部。冷藏以后的黄瓜果实冷害指数、电导率、PLD活性、LOX活性均呈现为脐部最高,中部次之,肩部最低。与膜结合的Ca2+含量则从黄瓜脐部到肩部逐渐递增。结果表明,黄瓜果实从果肩到果脐的耐低温能力逐渐降低,果实冷害程度与PLD和LOX活性提高和膜结合钙离子浓度下降显著相关。     

Chilling requirements of Paeonia cultivars

Dormant second year potted plants of Paeonia ‘Coral Sunset’, ‘Monsieur Jules Elie’, and ‘Sarah Bernhardt’ were placed into three chilling regimes (constant 1, 4, or 7°C) for different durations (3, 6, 9, or 12 weeks) to ascertain their chilling requirements for shoot and flower production. Chilling was followed by forcing for up to 5 weeks at 18°C, then plants were maintained in a controlled greenhouse until flowering had finished. Mean number of shoots and flowers per plant were recorded and the time taken for shoots to sprout was calculated.Control plants (forced immediately without chilling) produced no shoots or flowers. For all cultivars, the proportion of plants that sprouted, and the mean number of shoots and flowers increased as plants were subjected to colder chilling temperatures, or longer chilling durations. However, there were no significant within-cultivar differences between different treatments of 9 weeks or more. The time taken for sprouting to occur after the completion of each chilling treatment consistently decreased as the duration of the chilling treatment increased. In most cases, lower chilling temperatures lead to more rapid sprouting once plants were placed in the 18°C forcing conditions.When a simple model was fitted where the chilling temperature and duration of each treatment was described by a cumulative normal curve rising from zero to some maximum value (or potential) once adequate chilling had been received, we found that temperatures of 4 and 7°C provided only 83 and 59%, respectively, of the chilling accumulated per unit time at 1°C. ‘Coral Sunset’, an interspecific hybrid early flowering type, required the greatest amount of chilling to sprout consistently, while ‘Sarah Bernhardt’, a very late flowering type, required the least. Of the three cultivars, ‘Sarah Bernhardt’ also required the least amount of chilling to achieve its potential shoot and flower numbers, while ‘Monsieur Jules Elie’, a mid-season flowering type, required the most chilling to achieve the same end for these two variables. This suggests that the response to spring temperatures as well as chilling influences the time of flowering.     

Effects of low oxygen short-term exposure at 15°C on postharvest physiology and quality of apricots harvested at two ripening stages

Summary

Apricots of two harvests (9–10° Brix and 13–14° Brix) were treated for 6 d at 15°C with 1%, 2% and 4% O₂ (low oxygen = LO) and then kept for 7 d and 5 d (respectively for the first and the second harvest) in air at 15°C (shelf life = s.l.). Control fruit were held continuously in air at 15°C or for 6 d at 5°C then moved to 15°C. In early harvest fruit, low O₂ (1% and 2%) for 6 d controlled ethylene production even after the transfer and consequently the fruit had lower SCC and were firmer. In fruit from the second harvest, only 1% O₂ atmosphere or control fruits at 5°C were able to control the rise of ethylene in s.l. and to reduce the increase of soluble solids content (SSC). A 1% O₂ atmosphere maintained acceptable firmness even during s.l. in fruit of both harvests. Respiration rate was better restricted by low temperature during the treatment but at the end of experiment no difference was observed among the samples. Colour of apricots was maintained only by 1% O₂ atmosphere or 5°C temperature both in the first and in the second harvest. Sensory evaluation of fruit of the first harvest revealed that only apricots kept at 15°C or in 4% O₂ were considered saleable. In the second harvest, apricots treated with 5°C and 1% O₂ were judged saleable. In conclusion, early harvest fruit does not benefit from low oxygen (1% and 2% O₂) because fruit does not reach the optimal SSC whereas for late harvest apricots the use of 1% O₂ at a higher temperature than that used commercially can be an alternative to low temperature as shipping treatment or short term storage.     

Induction of resistance to Penicillium digitatum and chilling injury in ‘Star Ruby’ grapefruit by a short hot-water rinse and brushing treatment

Summary

Postharvest heat treatments have been used for many years as alternatives to chemical control of fungal diseases and insect infestation of fruits and vegetables. In this study, the effects of a new hot-water brushing (HWB) treatment on the resistance of red grapefruit (C. paradisi cv. Star Ruby) to green mould decay caused by Penicillium digitatum (Pers.: Fr.) Sacc. and on the development of chilling injury (CI) symptoms during cold storage were examined. The HWB treatment comprises rinsing hot water on the fruits as they move along a belt of brush rollers. A twenty second HWB treatment at 59 or 62° reduced decay, after arti®cial inoculation of wounded fruit, by 52 or 70%, respectively, compared with control unwashed fruit, whereas rinsing and brushing the fruit with tap water (~20°) or with hot water at 53 or 56°, were ineffective. HWB treatments applied 1–3 d prior to inoculation were most effective in enhancing the disease resistance of fruit, but were much less effective when the fruit were inoculated on the same day or 7.d later. HWB treatments at 59 or 62° for 20.s also significantly reduced the CI index and the percentage of fruit displaying CI symptoms by 42 and 58%, respectively, after six weeks’ storage at 2° and an additional week at 20°. Furthermore, HWB treatments cleaned the fruit and improved its general appearance without causing any surface damage, and did not influence fruit weight loss, percentage of total soluble solids (TSS) in the juice, juice acidity or fruit colour.     

Chilling induced ethylene biosynthesis in ‘Hayward’ kiwifruit following storage

‘Hayward’ kiwifruit were stored at 0, 5, 10, 15 and 20°C for 5, 12 and 17 days before rewarming to 20°C for 10 more days. Ethylene and CO₂ production, ACC, ACC synthase (ACS) and ACC oxidase (ACO) activities, flesh and core firmness, soluble solids content (SSC) and flesh colour were measured. Kiwifruit stored at 0, 5, 10 and 15°C did not ripen, produce ethylene or show increases in ACS or ACO activity. Fruit stored for 5 days at the above temperatures, then rewarmed to 20°C, did not show any change during the following 10 days. Rewarmed fruit, pre-stored at 0–10°C for 12 days, started autocatalytic ethylene production within 24 h, followed by fruit ripening. Fruit stored at 15°C for 12 days needed 72 h to start ethylene autocatalyse and did not fully ripen during 10 days at 20°C. After 17 days storage at 0–15°C kiwifruit started autocatalytic ethylene production with no delay upon exposure to 20°C. Autocatalytic ethylene production correlated with increased ACC content, and increased activities of ACS and ACO. Fruit held continuously at 20°C started autocatalytic ethylene production after 19 days, with concomitant increases in ACC content, ACS and ACO activities and ripening. Respiration increased after rewarming, concomitantly with the increase in ethylene production.We concluded that exposing kiwifruit to chilling temperatures (0–10°C) for 12 days advanced ethylene biosynthesis and ripening when compared with fruit held continuously at 20°C. The advanced ethylene biosynthesis was due to increase ACS and ACO activities immediately upon rewarming of the fruit.     

Guazatine control of sour rot in lemons,oranges and tangors under various storage conditions

Guazatine (1-17-diguanidino-9-aza-heptadecane acetate) was compared with sodium orthophenylphenate (SOPP), sec-butylamine (2-AB), benomyl and tridemorph for the control of citrus sour rot (Geotrichum candidum) under local marketing, export, and ethylene (C₂H₄) degreening storage conditions. Guazatine at 25–125 mg/l gave better control than 20 g/l SOPP, 10 g/l 2-AB and 250 mg/l benomyl in artificially inoculated ‘Eureka’ lemons stored at 27° C and high humidity for 6 days. At 500 mg/l, guazatine gave better control than 20 g/l SOPP, 10 g/l 2-AB or 500 mg/l benomyl in dip-inoculated ‘Eureka’ lemons, treated and packaged as for export and stored at 7° C for 2 or 10 weeks. At 250 mg/l, guazatine provided better control than 20 g/l SOPP, 5 g/l 2-AB, 250 mg/l benomyl or 1000 mg/l tridemorph in artificially inoculated ‘Washington’ navel oranges held for 4 days under degreening-conditions of 27° C and 90% RH with added C₂H₄.     

Storage capability at different temperatures of lemons grown in Israel

For prolonged storage of lemons, the best temperature to avoid rots and physiological disorders such as internal browning and peel pitting, was 14°C; for short periods only, storage at lower temperatures, 2–8°C, did not cause damage. Physiological disorders appeared in storage earlier, the lower the storage temperatures, and in fruit picked at a less ripe stage. The general appearance of the fruit is better when stored at the lower temperature. Color development, chemical changes, weight loss, respiration rate and ethylene evolution during storage of lemons at different temperatures and stages of maturity were examined.     

Chilling-injury in cucumber fruits. I. Effects of storage temperature on symptoms and physiological changes

Cucumber fruits transferred to a warm temperature after chilling displayed various symptoms of chilling-injury. In cucumbers chilled to 0°C, vertical fine wrinkles and/or shallow pitting was observed, while after chilling to 5°C deep pitting and/or surface depressions were apparent. Moreover, in the 0°C fruit compared with 5°C fruit, a higher $\text{210}\text{264}$ mμ UV absorption ratio of leakage substances during chilling was observed. These results suggest that the causes of chilling-injury in the 0°C and 5°C fruit are distinct from one another. Weight loss after chilling, the amount of leakage substances, the exudate content from the cut surface of the fruit, redox potential, titratable acidity and respiratory activity were also checked after periods of chilling of 3 to 15 days.     

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.     

Aroma volatiles emission in relation to chilling injury in ‘Kensington Pride’ mango fruit

Summary

Mature green mango fruit (Mangifera indica L. ‘Kensington Pride’) were stored at 0, 5, 10, 15 or 20°C for 1, 3, 7, 14, 21 or 28 d to induce different levels of chilling injury (CI) and to elucidate its relationship with aroma volatile production. The fruit were removed from storage and allowed to ripen at 22 ± 1°C and CI index was assessed on fully ripe fruit. Aroma volatile compounds were estimated from the pulp of fully ripe fruit. CI index significantly increased as the storage temperature was lowered and the storage period was extended, particularly in the fruit stored at 0, 5 or 10°C. CI symptoms did not develop on fruit stored at 15 or 20°C. Fifty-six aroma volatile compounds were identified from mango fruit pulp using headspace solid phase microextraction (SPME) technique with gas chromatography (GC-FID) and GC combined with mass spectrometry (GC-MS). Among the 56 aroma volatile compounds, 25 were quantified using GC, which included monoterpenes (±-pinene, ²-pinene, myrcene, 2-carene, ±-phellandrene, 3-carene, ±-terpinene, limonene, ocimine, ³-terpinene, ±-terpinolene, and a-terpineol), sesquiterpenes (±-copaene, ±-gurjunene, trans-carophyllene, aromadendrane, ±-humulene, alloaromadendrane, ³-gurjunene, and ledene), hydrocarbon (p-cymene), esters (methyl octanoate and ethyl caprylate), aldehyde (decanal), and norisoprenoid (²-ionone). A significant reduction in total aroma volatiles, monoterpenes, sesquiterpenes, hydrocarbon, esters, aldehyde, and norisoprenoid production were observed in fruit stored at 0, 5, 10 or 15°C compared with fruit stored at 20°C. The degree of reduction in aroma volatile compounds depended on the severity of CI, induced with different storage temperatures and storage periods. In conclusion lower temperature storage induced CI in mango fruit and adversely affected the aroma volatiles production.     

Temperature effects on dormancy,bud break and spear growth in asparagus (Asparagus officinalis L.)

Summary

The effects of the length of chilling, chilling temperature and growing temperature on dormancy of asparagus crown buds and subsequent rates of spear growth were examined. The results showed that prior chilling enhanced bud break at low growing temperatures and stimulated the growth of spears.Thus, chilling should facilitate commercial production by hastening bud break and spear growth rates at lower temperatures. If sufficient chilling was given, the minimum temperature for rapid bud break was approx. 12.5°C for ‘Rutgers Beacon’ and ‘Jersey Giant’, and around 10°C for ‘UC 157’ and ‘Apollo’. The optimum chilling temperature appeared to be closer to 5°C than to 10°C or 2°C for ‘Rutgers Beacon’ plants grown at 12.5°C. Increasing the growing temperature had a significant effect on the relative spear growth rate (RSGR) in all cultivars. Prior chilling had no effect on the RSGR for ‘Dariana’ and ‘Apollo’; but, for ‘UC 157’, chilling plants at 5°C for 5 or 10 weeks increased growth rates at 12.5°C and at 20°C. These results demonstrate that release of bud dormancy and spear growth rates depended not only on the growing temperature, but also, at least in some cultivars at some temperatures, on the duration and temperature of chilling during the previous Winter.     

Differential propylene induced ethylene production in ‘Anjou’ pears during storage at chilling and non-chilling temperatures

Summary

‘Anjou’ pears were harvested from the Mid-Columbia Experiment Station, Hood River, Oregon, at 67 N firmness, stored at –1° or 20°C for 85 d and periodically tested for sensitivity to 0 or 500 µl l^?1 propylene for at least 14 d at 20°C. Climacteric ethylene of pears stored at 20°C remained at low levels and started rising on the 90th day. Pears chilled at –1°C required 70 d to ripen and produced climacteric ethylene immediately upon transfer to 20°C. The sensitivity of the fruit to exogenous propylene increased progressively with storage time at –1°C. However, the non-chilled fruit responded to propylene similarly to freshly harvested fruit during the first 55 d of storage, then similarly to –1°C-stored fruit up to 85 d. Anjou pear ripening events and the sensitivity of the fruit to exogenous propylene developed differently in storage at non-chilling temperature compared with chilling temperature.     

Polyphenoloxidase activity during ripening and chilling stress in ‘Manila’ mangoes

Summary

‘Manila’ mangoes were stored at 6 or 12°C, while a control lot was ripened at 258C. Polyphenoloxidase activity was measured in pulp and peel of mangoes during normal ripening and chilling-stress conditions. Compositional parameters (textural hardness, pH, acidity, and soluble solids) were monitored during ripening and chilling injury (CI) was assessed by visual inspection. PPO activity increased in refrigerated mangoes but fruit stored at 6°C displayed greater activity than those stored at 12°C. Both temperatures produced a peak in enzyme activity at day 16 of storage. Peel browning and acidity correlated with PPO activity (r.=.0.9073 and 0.9818) at 6°C. After the PPO peak was observed at day 16, refrigerated mangoes showed lower enzyme activities; however external browning became more pronounced.     

Intermittent warming of peaches reduces chilling injury by enhancing ethylene production and enzymes mediated by ethylene

SUMMARY

Peaches (Prunus persica ‘Hermoza’) were ripened at 208>C after harvest and either stored at 08C for four weeks (control) to induce chilling injury or given intermittent warming (IW) on the twelfth day of storage (28C for 24.h) to alleviate chilling injury (CI). Continuously stored fruit from control developed wo olliness, a CI disorder, during ripening at 208C after cold storage while only a small percentage of IW fruit developed woolliness. CI fruit produced less ethylene during ripening after storage, and this inhibited ethylene production was closely tied with woolliness development. The IW treatment caused enhanced ethylene production in the fruit when returned to 08C and the ethylene remained higher than control fruit until the end of the storage period. IW also induced the messages for 1-aminocyclopropane-1-carboxylic acid oxidase (ACO) and 1-aminocyclopropane-1-carboxylic acid synthase (ACS) in the ethylene synthesis pathway. IW also elevated the mRNA of the cell wall degrading enzymes polygalacturonase (PG) and endo-1,4-gluconase (EGase). The mRNAs of the cell wall enzymes and the enzymes in the ethylene synthesis pathway remained higher even after 5.d at 08 C following the IW treatment. It is suggested that IW maintained the fruit tissue capacity to ripen normally by preventing inhibition of the ethylene synthesis pathway which occurred in the control fruit after extended storage.