Effect of storage temperature on ripening and quality of custard apple (Annona squamosa L.) fruits

Summary

The effect of storage temperature on ripening, shelf life and chemical composition of custard apple (Annona squamosa L.) fruits stored at 10,15,20 and 25°C was studied. The safe range of storage temperature was found to be between 15 and 20°C, with maximum shelf life at 15°C. The ripening of fruits was observed on days 4, 6 and 9 of storage at 25,20, and 15°C respectively. The colour of the pulp, texture, taste and flavour of ripe fruits held at 25 and 20°C were superior followed by fruits stored at 15°C. At 10°C, the fruits became hard with surface blackening, messy pulp and less sweetness. The major changes during ripening were a continuous decrease in fruit firmness and starch content and a continuous increase in TSS and sugars, the changes being more rapid at 25 and 20°C than at 15 and 10°C. The acidity and ascorbic acid contents increased slightly during the initial stages of ripening followed by a decline, in the fruits stored at different temperatures. Custard apple fruits stored at 25 and 20^CC had a clear climacteric peak whereas those stored at 15 and 10°C did not show any distinct rise in respiration rate. Ethylene peak (2.40 µl kg^–1 h^–1) coincided with the respiratory climacteric at 25^CC storage, corresponding with the peaks in TSS, sugars, ascorbic acid and acidity.     

Einfluss von Biostimulanzien und Lichtreflexionsfolie auf die Fruchtqualität und Farbentwicklung bei Apfel

The aim of this research was to improve inner and external fruit quality and fruit colouration using four-year-old apple ‘Braeburn, Hillwell’ trees on M9 (3?m × 1?m spacing) by employing reflective ground covers and biostimulants at Klein-Altendorf, nr. Bonn, Germany (50°N). Two reflective ground covers were spread on both sides of tree rows seven weeks before anticipated harvest and two biostimulants were applied two times – four and two weeks before harvest. Adjacent trees of the same row without reflective ground cover or without biostimulants served as control.Reflective ground covers significantly improved red colouration from 71°hue in the control to 49°hue with the ground cover Lumilys® and to 40°hue with Extenday®. The red colouration of the lower surface of fruits improved from 85°hue in the control to 52°hue with Lumilys® and 40°hue by Extenday®. Apple trees with Extenday® and Lumilys® produced 69% and 44% well-coloured fruit (with 75–100% fruit colouration) compared with 16–26% in the control.By contrast, an acceleration of ripening processes was not observed in plots with reflective ground covers compared with the control. There were no differences in sugar contents (°Brix) and fruit firmness (kg/cm²), but starch breakdown in fruit with reflective mulch was significantly delayed compared with the control resulting in retarded maturation.An economic analysis based on material costs and lifespan – excluding the labour costs for spreading and removing the ground covers – showed an economic advantage, if these mulches are used more than once a year.Both biostimulants showed neither effects on inner and external fruit quality nor on fruit colouration. Fruits with Wuxal®ATRiun or Sunred® did not improve the percentage of well-coloured fruits (75%–100% fruit surface with red colouration) compared with the untreated control. Similarly, inner and external fruit quality showed no significant differences in fruit firmness, sugar content and starch degradation. An economic analysis based on chemicals’ costs – excluding the labour costs for applying the biostimulants – resulted in no economic advantage. The chlorophyll – based ‘Index of Absorption Difference’ (IAD; measured non-destructively by the DA-meter) in some cases correlated positively with the Streif (maturation) index based on destructive assessment fruit firmness, sugar content and starch breakdown in an ‘ART system’.     

Subatmospheric pressure storage of mango fruits

Ripening of mango fruit is markedly delayed when the pressure in the storage chamber is reduced below 100 mm Hg, and fruit storage life is thus prolonged. The prolongation of storage life is inversely related to the pressure; control fruit stored at 760 mm Hg started to ripen after 16 days in storage at 13°C, while fruit stored at 100 and 75 mm Hg after 25 and 35 days, respectively. Fruit stored at 50 mm Hg remained unripe for 35 days. No effect on ripening was recorded at pressures above 250 mm Hg, while at pressures below 50 mm Hg the fruit desiccated. All fruits stored at subatmospheric pressure ripened 3–4 days after transfer to shelf life at 25°C. However, green mango fruits of the colored cultivars like ‘Haden’ and ‘Maya’, stored at subatmospheric pressure for a prolonged period, did not develop the proper red or orange color during shelf-life, but turned pale yellow instead. Treatment with ethylene upon removal from storage slightly improved color development in these fruits.     

Storage of some local and introduced mango cultivars grown in Trinidad

The fruit characteristics and storage potential of some local and introduced mango cultivars grown in Trinidad were compared. At ambient temperature (28–32°C), fruit could be stored satisfactorily for between 3 and 8 days, after which ripening rapidly occurred. At 14°C, storage life was increased to as much as 18 days (cultivar ‘Graham’). Enclosure of fruits individually in polythene bags increased storage life at either ambient or 14°C temperature, while treatment with 3% Sta-fresh wax increased storage at ambient but not at 14°C. In the case of ‘Doodooth’, which was highly susceptible to anthracnose, treatment of fruit with hot water (52 ± 2°C) containing 500 or 1000 mg l^?4 benomyl for 5 min reduced the incidence of disease. Results are discussed in relation to the export potential of mangoes.     

Preventing cold storage disorders in nectarines

A storage experiment was aimed at preventing low temperature storage disorders in nectarine fruits, of cvs July Red and Autumn Grand. Fruit was either cooled immediately after harvest or kept at 20°C for 48 h, before transfer to controlled atmosphere (CA) conditions at 0°C. Combinations of 0, 10, 15 and 20% C02 with 8 and 16% 02 were assayed. The fruit was evaluated following cold storage, 31 days after harvest, and after four and eight days under ‘shelf conditions’ (ripening at 15-18 °C). Warming of the fruit at 20°C before cold storage prevented woolliness in the absence of elevated C02 levels but did not affect internal browning and increased reddish discoloration; further, it enhanced water loss and ripening, increasing fruit softening markedly. Conversely, high C02 delayed fruit ripening in CA storage, keeping the fruit firmer, and preventing the development of woolliness, internal browning and reddish discoloration during ripening, the best results being mostly obtained with 20% C02. 02 levels assayed did not show clear effects, but decreased 02 concentration in absence of high C02 showed some benefit in ‘July Red’. No deleterious effect of C02 concentrations even as high as 20% could be detected. Thus, even though high C02 in CA conditions showed promise for controlling disorders and preventing over-ripening, further work is needed on other cultivars, and lower 02 concentrations should be investigated before making a general recommendation.     

Effect of different temperatures on the storage of papaya fruits and respirational activity during storage

Mature papaya fruits were stored at 10 and 15°C to study the effect of these temperatures on the storage and of respirational activity during storage. Percentage weight loss of fruits increased with prolonged storage period, and the increase was greater in fruits stored at 15 than at 10°C. The decay percentage was greater at the higher temperature than at the lower temperature. Total soluble solids showed a slight and gradual increase upto the end of the storage period. The high storage temperature accelerated colour development in the peel and total chlorophyll diminished. There was an increase in total carotenoids in both the peel and the pulp as the storage period increased, and the rate of increase was greater at the higher temperature.The respiration rate was relatively low at the beginning of ripening and tended to level off until the 11th and 12th day of storage, which were followed by a striking increase until it reached its maximum rate at the over ripe stage.     

Effect of temperature manipulation during storage and ripening on firmness,extractable juice and woolliness in nectarines

‘Independence’ nectarines were stored at — 0.5°C for three or four weeks or at 3°C for four weeks or kept at room temperature for 18 h prior to storage for four weeks at -0.5°C. After cold storage, fruit from all treatments was ripened at 10°, 15°or20°C. In all treatments the percentage woolly fruit initially increased to high values and thereafter decreased with further ripening. The rate of increase and decrease in woolliness depended on the ripening temperature. A storage period of four weeks at — 0.5°C resulted more woolliness during subsequent ripening. Woolliness persisted longer after a four-week cold storage period than after a three-week one. When fruit was delayed at room temperature prior to cold storage, woolliness generally developed earlier and to a lesser extent during ripening. At all ripening temperatures initial storage at 3°C resulted in most woolliness extending over the longest period. In addition, browning of the meso- carp tissue occurred only in fruit cold stored at 3°C.-The delay period before cold storage decreased fruit firmness by 15.7 to 17.6 N. Except for fruit subjected to the delay period, the extractable juice in fruit of all treatments first decreased during ripening to low values then increased.     

Effect of gibberellic acid and Vapor Gard on ripening,amylase and peroxidase activities and quality of mango fruits during storage

Post harvest application of gibberellic acid at 200 mg 1^?1, Vapor Gard (di-l-p-menthene) at 2.5% and their combination was studied on ‘Mallika’ mangoes (Mangifera indica L.) stored at ambient temperature (37 ± 2° maximum and 34 ± 2°C minimum) and at 15°C. Significant delay in the ripening of mango fruits was observed when gibberellic acid was applied with or without Vapor Gard. Gibberellic acid significantly retarded the degradation of ascorbic acid and chlorophyll in the peel, and reduced a-amylase and peroxidase activities during storage. Loss of weight decreased following treatment with Vapor Gard either alone or with gibberellic acid during storage at both ambient temperature and at 15°C. A pronounced retardation of ripening was observed when fruits were treated with gibberellic acid and Vapor Gard and stored at 15°C. The study thus suggests that mango fruits can be successfully stored for 20 d by application of gibberellic acid (200 mg 1^?1) in combination with Vapor Gard (2.5%) and stored at 15°C.     

Hydrolytic and oxidative enzymes during banana ripening

The relative activities of 5 hydrolytic and oxidative enzymes, viz. alpha-amylase, starch phosphorylase, acid phosphatase, peroxidase and catalase, increased considerably in 3 cultivars of banana fruits stored for 5 weeks at 20°C. An upsurge in the activities of all the enzymes, having as a maximum about 1.2–19.1 times their initial level, was observed during the ripening at 20°C. The 3 banana cultivars differed greatly in the activities of all the 5 enzymes studied.     

Effects of Fertigation on Pigment Pattern and Fruit Quality of cv. ‘Gala’ Apples

Fruit pigmentation in ripening cv. ‘Gala, Schniga’ apples was monitored under the influence of fertigation weekly during 21 July–31 August 2009, i.e. 34 days before and 7 days after the optimal harvest date in Slovenia. The soil was a heavy loam clay with high humus content (2.8 %) and high acidity (low pH 4.9). The spectral indices NDVI (Normalized Difference Vegetation Index) and NAI (Normalized Anthocyanin Index) were obtained by a PA 1101 on attached fruit on the transition between the ground and blush colour of the fruit surface. NAI increased slowly from 0.25 to 0.6 two weeks prior to optimum maturity. NDVI values fell from 0.9 to 0.2 before and during ripening, with significant changes starting ca. 3 weeks before and during the week after the optimum harvest date. Fertigation delayed fruit ripening viz harvest date by ca. 4 days. Fertigation delayed changes in the intensity of the fruit’s epidermal pigments, expressed as NDVI for 1 week and NAI for 4 weeks, respectively, but had no significant effect on fruit colour or NDVI and NAI values at the optimal harvest date. At this time, those fruits from the fertigated trees were firmer with a lower starch index compared with the un-fertigated control. Statistically, highly significant correlations were found (p?≤?0.01) (r?=?0.35 to r?=?0.91, R²?=?0.11–0.83) between all the studied spectral and standard parameters i.e. fruit fresh firmness, soluble solids content and starch index.     

Physiological and biochemical studies on chilling-injury of banana

Storage of banana fruits at low temperature was unsuccessful due to chilling-injury. Titratable acidity and respiration of banana fruits remained lower at 5°C than at room temperature and accompanied the prevention of ripening and chilling-injury. Dopamine (3,4-dihydroxyphenylethylamine) was the only major phenolic constituent in banana peel; low temperature might induce its oxidation to dark coloured substances.     

晚熟白肉水蜜桃新品种——秋月的选育

秋月是以大白凤为母本,白香露为父本杂交选育而成的晚熟白桃新品种。在上海地区果实成熟期为8月上中旬,果实生育期为130 d,较川中岛晚熟7~10 d。果实近圆形,黏核,平均单果质量208 g,大果质量275 g;果皮底色白色,盖红色程度约25%。果肉白色,汁液多,溶质,可溶性固形物含量13.5%~14.5%,风味优良。秋...     

The effect of day and night temperatures on the growth,development and yield of glasshouse cucumbers

The responses of January-sown cucumber cvs Farbio and Sandra to day and night temperature during the early post-planting stage (late February to mid-April) were examined in a glasshouse experiment. Three day temperatures (15°, 20° and 25°C) were combined factorially with three night temperatures (10°, 15° and 20°C). Comparisons were also made between two temperature regimes (21°C day: 19°C night and 24°C day: 17°C night) applied during the pre-planting stage (late January to late February) and between two mainstem cropping methods (restriction or retention of mainstem fruits). In the pre-planting stage the 24°C day: 17°C night temperature combination produced plants which were taller, heavier and leafier than those grown at 21°C day: 19°C night. During the first 12 weeks of harvesting the larger plants produced significantly more fruit and higher gross monetary returns than did their smaller counterparts. The difference then diminished and after 20 weeks of harvesting plants from the two pre-planting temperature treatments had produced similar weights of marketable fruit of equivalent value. In the early post-planting period increases in total leaf area and stem length were closely correlated with 24-h mean temperature. Earliness (first harvest) and total weight of fruit after four weeks of harvesting were also linearly related to mean post-planting temperature. Raising the 24-h mean air temperature (within the range 15.2° to 22.6°C) by 1°C during the early post-planting stage increased early (4 week) yield by 0.82 kg m^-2 and total (20 week) yield by 1.17 kg m^-2. There was no effect of day/night temperature amplitude. After 20 weeks of harvest, gross monetary returns and profitability were generally highest when mean temperature in the early post-planting period was high and fell progressively with reduced mean temperature. Restricting stem fruits to oné per leaf node produced no significant difference in either the yield or quality of fruit from plants of any of the temperature treatments. The results are discussed from physiological and practical viewpoints and a cost-benefit comparison of temperature treatments is presented.     

Effects of pre- and post-bloom temperature regimes on development of Lilium longiflorum Thunb.

Glasshouse grown ‘Ace’ and ‘Nellie White’ Easter lily plants were subjected to different temperature regimes to determine temperature requirements during pre- and post-bloom development. Rate of leaf- and flower-bud development and stem elongation on the primary (mother) axis were directly proportional to the range of temperatures used (6–24°C), and were equally effective in predicting crop development. Scale initiation on the secondary (daughter) axis during pre-bloom phases was proportional to growing temperature, reaching maximum activity at 18°C in ‘Ace’ and at 12°C in ‘Nellie White’. The shift from scale to leaf initiation and development following anthesis was favored by 12 rather than 18°C with significant reductions in leaf initiation in both cultivars at 24°C. No difference in secondary meristem diameter occurred with temperature during pre-bloom, but large dome size was associated with 12°C or lower during the post-bloom phase. Primary scale weight increase (filling), reached a maximum 50 days following anthesis, and was greatest at 18°C. Secondary scale filling reached a maximum 80 days after anthesis at both 18 and 24°C. The secondary axis became increasingly responsive to sprout-inducing temperatures with increasing age and development. Fifty days after anthesis, 12 and 18°C were equally effective in sprouting ‘Ace’ bulbs, while 12°C was more effective with ‘Nellie White’. Early leaf senescence, associated with high (24°C) temperature, did not favor increased bulb size, daughter leaf primordia count and meristem diameter, or sprouting.     

Comparison of changes in sugars and ethylene production of cherimoya fruit grown at different seasons

Summary

Changes in fruit weight, total soluble solids (TSS), sugar content and postharvest ethylene production during fruit development were compared on fruit of cherimoya (Annona cherimola Mill., cv. Big Sister) pollinated at different times (early, at the beginning of April, 1995 and late, at the end of May, 1994). Fruit weight increased by growth, independently of pollination times. Changes in TSS and sugar content were strongly affected by pollination time. In late pollinated fruits, both TSS and sugar content increased during the growth period, 110–160 d after pollination, while neither increased with fruit growth in early pollinated fruit. Moreover, changes in TSS and sugar content after ripening depended not only on pollination time but also on the growth period. With late pollination, fruit harvested after 140 d became edible after ripening. The TSS and total sugar contents, (the sum of fructose, glucose and sucrose contents) increased to about 20° Brix and above 16%, respectively. But early pollinated fruits were not edible after ripening, since total sugar content increased only to about 7%, even though they kept growing for 160 d on the tree. The maximum rate of ethylene production declined and the number of days to the ethylene peak from harvest is also reduced with growth in both cases. These changes were closely correlated with days after pollination (r>0.9) regardless of pollination time. Comparisons of accumulated temperature suggest that temperature at pollination time and during the resting period of growth affected fruit development. These results indicate that neither fruit weight nor number of days after pollination is a suitable index for harvesting time.     

Amount of Cortical and Epidermal Tissue Shed From Roots of Apple

Rates of CO₂ production by cv Idared apples were progressively reduced by lowering O₂ levels from 21% to 2% and 1%. Although lowering the temperature from 4° to 2°C also reduced the respiration rate, fruits stored in 1% and 2% O₂ were respiring faster after 100 days at 0°C than at 2° or 4°C. After 192 days the air-stored fruit also showed an increase in respiration rate at 0°C. These higher respiration rates preceded the development of low temperature breakdown in fruit stored in air, 2% and 1% O₂ at 0°C and in 1% 0₂ at 2°C. Progressively lower O₂ concentrations reduced ethylene production whilst increasing the retention of acid (expressed as malic), soluble solids, chlorophyll and firmness. In the absence of low temperature breakdown the effects of reduced temperature on fruit ripening were similar to those of lowered O₂ concentrations. The quality of apples stored at 4°C in 1% O₂ was markedly better than in 2%; the fruits were also free of core flush (brown core) and other physiological disorders.     

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.     

Ca storage and hypobaric storage of white peach ‘Okubo’

White peach ‘Okubo’ fruits were stored for 3 weeks at 1°C in cold storage, controlled atmosphere (CA) storage (3% CO₂ + 3% O₂ and 0% CO₂ + 3% O₂) and hypobaric storage ($\text{1}\text{7}\text{and}\text{6}\text{7}\text{atm}\text{.}$) After removal from storage, fruits were ripened at 20°C. In cold-stored fruits, low temperature injuries (flesh browning, mealy breakdown and abnormal peeling) developed. When O₂ was maintained at 3% without CO₂, the ripening rate after storage was faster than that of fruits which had been held at 20°C directly, and low temperature injuries were not controlled. Under the atmospheric conditions of 3% O₂ and 3% CO₂, ripening rate after storage was not different from that of directly ripened fruits, and injuries were almost completely controlled. In the fruits kept in hypobaric storage of $\text{1}\text{7}\text{atm}\text{.}$, the ripening rate after storage was slower than that of fruits stored in air at 1 atm. (cold storage). Mealy breakdown was reduced, but no effect was found on the flesh browning nor on the abnormal peeling. No significant differences were found between hypobaric-stored fruits of $\text{6}\text{7}\text{atm}\text{.}$ and cold-stored ones.     

早熟黄桃新品种——锦香的选育

从北农二号×60-24-7的杂交后代中选育出早熟鲜食黄肉桃新品种锦香。锦香无花粉,果实发育期为80d,在上海地区果实成熟期为6月下旬。果实圆形,单果平均重193g,大果重270g。果皮底色金黄,着色约25%,茸毛少。果肉金黄色,可溶性固形物含量9.2%-11%,风味甜,微酸,香气浓,黏核。在上海、浙江、江苏等地已有一定的推广面积。     

Early forcing of narcissus: The effects of lifting date and stage of floral development at the start of cooling

Early Narcissus flowers may be obtained if bulbs are lifted early from the field, warm-stored (35°C) and then cool-stored (9°C) before forcing in a glasshouse. The earliest satisfactory forcing was investigated, in ‘Carlton’ and ‘Fortune’, by lifting weekly from 27 May to 22 June, and storing at 17°C for 0–7 weeks between warm- and cool-storage. Storage at 17°C is usually intercalated to allow the completion of flower differentiation prior to the start of cool storage.After warm-storage, the bulbs lifted on 27 May and 22 June had reached Stages Sp and A2 of flower differentiation, respectively; 5–7 weeks of 17°C-storage were then needed to reach complete flower differentiation (Stage Pc). Cool storage was therefore begun with bulbs ranging from Stage Sp to Stage Pc. The earliest cooled bulbs had progressed only to Stage A2, and all others to Stage Pc, after 14–16 weeks of cool storage. No floral defects (e.g., split paracorolla) were noted in any treatment, but in ‘Carlton’, about half the bulbs lifted on 27 May and stored for 0 or 1 week at 17°C did not yield a flower, due to failure of the scape to elongate and death of the flower bud within the spathe.Duration of the glasshouse period was reduced by later lifting and by longer 17°C-storage, but following lifting on 15 or 22 June and 2 or more weeks at 17°C, differences were trivial. For flowering within 30 days in the glasshouse, 5 or 6 weeks' 17°C-storage was needed with 27 May lifting, reducing to 1 week at 17°C after 22 June lifting. Flowering within 21 glasshouse days was achieved only after 15 or 22 June lifts followed by 4–5 weeks at 17°C. The earliest flowers in ‘Fortune’ (7 November) were produced following 3–5 weeks at 17°C after lifting on 27 May or 1 June, or following 1–2 weeks at 17°C after later lifting. In ‘Carlton’, the earliest flowers (23 November) followed 2–3 weeks at 17°C after lifting between 1 and 15 June, or 0–1 weeks at 17°C after the last lifting date (22 June). Following the use of 3 weeks' 17°C-storage, flowering date was about equal, irrespective of lifting date. However, further extension of 17°C-storage resulted in a delay in flowering date. Scape length increased irregularly with longer storage at 17°C; scapes were taller following later lifting (8–22 June) than following earlier lifting. Differences in flower diameter between treatments were relatively small.