Investigating the potential of a humidification system to control moisture loss and quality of ‘Crimson Seedless’ table grapes during cold storage

The potential of humidifying cold storage rooms to control moisture loss and quality of table grapes in different package designs was studied. Fruit were stored in cold rooms (−0.33 ± 0.32 °C or −0.12 ± 0.32 °C) with humidifier (95.0% RH) or no humidification (90.3% RH) respectively. Room humidification resulted in a 7.5% and 9.0% increase in RH inside the clamshell and open-top punnets multi-scale packages respectively in comparison to non-humidified storage, while there was no significant change in RH inside the 4.5 kg carry bag multi-packaging. The grapes were assessed for weight loss and SO₂ injury at intervals during a 35 d period. After 21 d of cold storage under humidification, weight loss of grapes was significantly higher (P < 0.05) in packages with open-top punnets than clamshell punnets and carry-bags. After 35 days in non-humidified cold storage, grape weight losses were 1.45 ± 0.32%, 1.62 ± 0.21% and 2.01 ± 0.57% for the 4.5 kg carry-bag, 5 kg clamshell punnet and 5 kg open-top multi-packages, respectively. When fruit were stored inside the same types of multi-packages under humidification, the corresponding weight losses were 0.97 ± 0.34%, 1.08 ± 0.27% and 2.00 ± 0.57%. Cold storage humidification reduced the rate of stem dehydration and browning; however, it increased the incidence of SO₂ injury in table grape bunches and caused wetting of the packages.     

Effect of initial hermetic sealing on quality of ‘Kyoho’ grapes during storage

Experiments of initial hermetic sealing using high barrier film were carried out on ‘Kyoho’ grapes (Vitis vinifera L. × V. Labrusca L. cv. Kyoho) in the 2008 and 2009 fruit seasons, to investigate their potential to enhance quality and extend storage life of the fruit. In the 2008 season, grapes were packaged in high barrier film bags for 1, 2, 3, 4 and 5 weeks, and a modified atmosphere (MA) of low oxygen and high carbon dioxide was formed after sealing. After packaging, fruit were removed from bags and stored in air for up to 90 d at 0 °C. In the 2009 season, grapes were packaged in perforated bags, or in high barrier film bags for 2 weeks and subsequently perforated bags to avoid further anoxia and excessive CO₂ accumulation. After treatment, fruit were stored for up to 90 d at 0 °C, followed by shelf-life at 20 °C for 7 d. Non-packaging air storage was used as a control in both seasons. Fruit quality attributes including soluble solids, titratable acidity, stem browning, berry drop and decay incidence were measured. The results indicated that short-term initial MAP (≤2 weeks) had potential for improving appearance of bunches and maintaining the quality of berries during long-term storage, and significantly reduced quality deterioration. Stems were greener and berry drop and decay incidence were more effectively controlled when fruit were sealed in high barrier film bags for 2 weeks and the bags were subsequently perforated.     

Applications of salt solutions before and after harvest affect the quality and incidence of postharvest gray mold of ‘Italia’ table grapes

The efficacy of some potassium and calcium based salts, namely potassium sulphate (PS), potassium sorbate (PSo), potassium carbonate (PC), potassium bicarbonate (PB), calcium sulphate (CS), calcium chelate (CCh), calcium chloride (CC) and calcium silicate (CSi) against gray mold of ‘Italia’ table grapes, was evaluated. In in vitro experiments, PSo, PC, PB, and CCh completely inhibited mycelial growth of Botrytis cinerea at 0.25%. Under artificial inoculation, salts at 1% (immersed or sprayed) showed a variable effect against the pathogen. For natural infection, salt solutions (1%, w/v) were applied according to three strategies: (a) spray (one week) before harvest, (b) immersion after harvest, and (c) combined treatments spray and immersion. The decay incidence of gray mold was evaluated after 30 days at 2 ± 1 °C and 90–95% RH, followed by 7 days of shelf-life at 22 ± 2 °C. All tested salts significantly reduced the decay incidence of gray mold as compared to a water control for the three strategies. The percentages of reduction ranged between 77–100, 91–98, and 61–100% for the preharvest treatment, in combined application, and in the postharvest treatment, respectively. PB and PSo were the most effective salts, completely inhibiting development of gray mold when applied before harvest and as a postharvest treatment. The influence of salts on physical and chemical properties of berry quality including total soluble solids, titratable acidity, pH, color index, weight losses and microbiological profiles was also investigated. New strategies are needed with the critical goal of controlling gray mold of grapes with no fungicide residues. Salts applied just before harvest may be an effective way to minimize gray mold during storage.     

Prestorage application of high carbon dioxide combined with controlled atmosphere storage as a dual approach to control Botrytis cinerea in organic ‘Flame Seedless’ and ‘Crimson Seedless’ table grapes

Pre-storage application of 40% CO₂ at 0 °C for 24 or 48 h and controlled atmosphere (12% O₂ + 12% CO₂) storage at 0 °C for up to eight weeks on decay control and quality of organic ‘Flame Seedless’ and ‘Crimson Seedless’ table grapes were studied as a postharvest disease control alternative. To simulate different potential field conditions, these organic treatments were applied to organic-grown grapes that were naturally infected (without inoculation), surface inoculated (berries inoculated by spraying with a conidia suspension), and nesting inoculated (clusters inoculated by placing in the middle an artificially infected berry) with the pathogen Botrytis cinerea, the cause of grape gray mold. Under these three conditions, a 40% CO₂ for 48 h pre-storage treatment followed by controlled atmosphere reduced the gray mold incidence from 22% to 0.6% and from 100% to 7.4% after four and seven weeks, respectively. High CO₂ pre-storage alone limited botrytis incidence in both naturally and artificially infected grapes, but was more effective when combined with CA. These treatments did not affect visual or sensory fruit quality. Exposure to high CO₂ for 24 or 48 h effectively inhibited mycelial growth of B. cinerea in PDA plates incubated at 22 °C for up to 72 h. Conidia germination in PDA plates was reduced ∼60% after 12 h incubation. In vitro studies demonstrated a fungistatic effect, but further studies on the mechanism of action could improve treatment performance. This novel high CO₂ initial fumigation followed by controlled atmosphere during storage or transportation could be a commercially feasible alternative for postharvest handling of organic and conventional table grapes. Our results encourage validating this combined physical treatment in other cultivars and under commercial conditions.     

Internal browning disorder and fruit quality in modified atmosphere packaged ‘Bartlett’ pears during storage and transit

Internal browning (IB) can be a serious problem with the use of modified atmosphere packaging (MAP) for ‘Bartlett’ pears (Pyrus communis L.) grown in the Pacific Northwest during storage and transit to distant markets. To investigate this disorder, ‘Bartlett’ pears harvested at commercial maturity were packed in a commercial MAP (MAPc), an experimental MAP (MAPe) and commercial perforated plastic bags (control) and stored in air at −1.1 °C. After 1 and 3 months of storage, samples of MAPc and control fruit were transferred to rooms at temperatures of 2, 4.5, 7.5, and 10 °C for 3 weeks to simulate transit temperatures and the time required to reach distant markets. MAPc maintained an average internal atmosphere of 12.3% O₂ + 5.6% CO₂ and significantly extended ‘Bartlett’ pear storage life with high eating quality and without IB and other disorders for up to 4 months at −1.1 °C. The internal gas atmosphere of MAPe equilibrated at 2.2% O₂ + 5.7% CO₂, which resulted in fruit with 25.5 and 62.3% IB after 3 and 4 months of storage, respectively. During simulated transit conditions of 2, 4.5, 7.5, and 10 °C, the CO₂ level in MAPc was maintained at 5.6–7.9%, while O₂ was reduced dramatically to 10.5, 5.0, 2.5, and 1.0%, respectively. IB developed at 7.5 and 10 °C but not at 2 and 4.5 °C, regardless of pre-transit storage duration (1 and 3 months) at −1.1 °C. The longer the storage duration and the higher transit temperature, the higher the incidence and severity of IB. The MAP-related IB disorder observed in this study included two types of symptoms: classic pithy brown core and wet brown flesh. The MAPc storage gas atmospheres maintained fruit firmness, color and higher eating quality after ripening, eliminated senescent scald and core breakdown, suppressed the loss of ascorbic acid (AsA) and titratable acidity, and slowed the accumulation of malondialdehyde (MDA) during storage at −1.1 °C for up to 4 months or 3 months + 3 weeks at simulated transit temperatures of 2 and 4.5 °C. In contrast, fruit held in MAP with low O₂ levels (1.0–2.5%) developed IB that appeared to be associated with a reduction in AsA, accumulated MDA and exhibited an increase in membrane leakage. MAP inhibited ripening at high CO₂ + high O₂ but lead to IB when the packaging material or elevated temperatures resulted in high CO₂ + low O₂ conditions. The incidence of IB closely correlated with lipid peroxidation and appeared to be related to fruit AsA concentration. The MAPc designed for pears appears to be suitable for ‘Bartlett’ fruit stored at −1.1 °C for up to 4 months or storage for 3 months and a transportation duration of up to 3 weeks at 0–4.5 °C during the early season and at 0–2 °C during the late packing season. These conditions yielded fruit of high eating quality and without IB or over-ripening upon arrival at distant markets.     

Canopy position affects rind biochemical profile of ‘Nules Clementine’ mandarin fruit during postharvest storage

This study was conducted to investigate the effects of preharvest canopy position and bagging treatments on rind physiological and biochemical properties of ‘Nules Clementine’ mandarin (Citrus reticulata Blanco) fruit. Before storage, the respiration rate of unbagged outside fruit was significantly higher (21.6 mL CO₂ kg⁻¹ h⁻¹) than of bagged inside fruit (16.3 mL CO₂ kg⁻¹ h⁻¹). Unbagged fruit outside the canopy had 1.4-fold higher carbohydrates, and 1.1-fold higher dry matter (DM) content than bagged inside fruit. Bagged fruit inside the canopy had higher (24%) weight loss than outside sun-exposed fruit (14%). This corresponded with a higher rind breakdown (RBD) index for bagged inside fruit, compared to sun-exposed fruit which did not develop the disorder. During postharvest storage, rind fructose levels of bagged fruit inside the canopy increased from 62.4 mg/g DM at harvest to 81.3 mg/g DM after 8 weeks, while those of unbagged outside fruit increased from 97.9 to 108.4 mg/g DM. Concomitant with the increase in fructose, sucrose in rind tissue of bagged inside fruit decreased from 42.6 to 27.7 mg/g DM and from 49.3 to 33.4 mg/g DM for unbagged outside fruit. Rind glucose of unbagged inside fruit decreased from 90.6 to 76.2 mg/g DM. Ascorbic acid concentrations remained almost constant during storage, with levels between 3.3 and 6.7 mg/g DM for inside bagged and unbagged outside fruit, respectively. Hesperidin was the major flavanone detected, with concentrations between 35 and 45 mg/g DM followed by narirutin (1.1–2.8 mg/g DM). At harvest, rind of fruit harvested from outside the canopy had lower hesperidin concentration (38.1 mg/g DM) compared to shaded fruit (44.2 mg/g DM). Overall, the results suggest that variations in microclimatic conditions inside the tree canopy during the growing season affect the biochemical profile of the fruit rind, which in turn influences fruit response to postharvest stresses associated with senescence and susceptibility to RBD.     

Ripening behavior and quality of modified atmosphere packed ‘Doyenne du Comice’ pears during cold storage and simulated transit

The effect of MAP on extending storage life and maintaining fruit quality was studied in ‘Doyenne du Comice’ (Pyrus communis L.) pears at Hood River and Medford, Oregon. Control fruit packed in standard perforated polyethylene liners started to show senescent core breakdown and lost the capacity to ripen at 20 °C after 4–5 months of cold storage in Hood River and after 5.25–6 months in Medford. LifeSpan^® L257 MAP achieved steady-state atmospheres of 15.8% O₂ + 3.7% CO₂ in Hood River and 15.7–17.5% O₂ + 3.8–5.7% CO₂ in Medford. MAP inhibited ethylene production, ascorbic acid degradation and malondialdehyde accumulation, and extended storage life for up to 6 months with maintenance of fruit flesh firmness (FF) and skin color without commercially unacceptable level of physiological disorders. After 4, 5 and 6 months at −1 °C, MAP fruit exhibited climacteric-like patterns of ethylene production and softened to proper texture with desirable eating quality on day 5 during ripening at 20 °C. After 6 months at −1 °C plus 2 weeks of simulated transit conditions, MAP fruit maintained FF and skin color and had good eating quality at transit temperatures of 2 and 4.5 °C (10.1–11.5% O₂ + 4.8–5.2% CO₂), but reduced FF substantially and developed internal browning disorder at 7.5 and 20 °C (3.2–7.2% O₂ + 7.9–9.5% CO₂). The storage life of ‘Doyenne du Comice’ pears with high eating quality could be increased by up to 2 months when packed in MAP as compared with fruit packed in standard perforated polyethylene liners.     

Changes in volatile production and sensory quality of kiwifruit during fruit maturation in Actinidia deliciosa ‘Hayward’ and A. chinensis ‘Hort16A’

Although volatiles have been previously studied in kiwifruit (Actinidia spp.), there has been no co-ordinated study of volatile release and softening through the full edible period. In this report, the two most important commercial cultivars A. deliciosa ‘Hayward’ and A. chinensis ‘Hort16A’ were evaluated for volatiles released at different ripening stages corresponding to their typical commercial shelf life, and compared to the sensory quality assessed by a trained taste panel. Gas chromatography–mass spectrometry data indicated that large amounts of straight-chain aldehydes and esters were the dominant volatiles in the two cultivars. In particular, butanoates, the main fruity esters in both fruit, significantly increased during ripening and an extremely high level of butanoates was found in the over-ripe fruit. Sensory results indicated that with fruit softening, some of the changes in volatile content could explain changes in fruit flavor detected by a trained panel, and differences in characteristic flavor of the two cultivars. The results have implications for fruit sample handling and volatile assessment.     

Dynamics of ascorbic acid in ‘Braeburn’ and ‘Gala’ apples during on-tree development and storage in atmospheres conducive to internal browning development

The underlying causes as well as chemical and biochemical alleviation for CO₂-induced browning in apple fruit are poorly understood. Ascorbic acid (AsA) dynamics in ‘Braeburn,’ a susceptible cultivar, and ‘Gala’, a resistant cultivar, were evaluated during on-tree development and storage at 0.5 °C in air or controlled atmospheres (CA) containing 1 kPa O₂ and 1, 3 or 5 kPa CO₂. ‘Braeburn’ fruit treated with diphenylamine (DPA) was also stored for 1 month to determine effects on browning incidence and AsA concentration. ‘Braeburn’ apples had significantly higher (p ≤ 0.05) AsA levels than ‘Gala’ during on-tree development, and storage. No correlation between AsA and maturity/ripening indices for ‘Braeburn’ or ‘Gala’ was apparent. Histochemical localization of fruit AsA showed a staining intensity consistent with the quantity analytically determined, and showed that AsA is diffusely distributed throughout the cortex in both cultivars during on-tree development. During storage, AsA was localized to the periphery of brown tissue in ‘Braeburn’ and to the coreline and cortex proximal to the peel in ‘Braeburn’ and ‘Gala’ tissues. DPA decreased browning development during storage, however, no correlation between DPA treatment and AsA quantity in healthy or brown cortex tissue was observed. The results indicate AsA quantity alone is not an indicator of CO₂ sensitivity in these two cultivars.     

Effects of cold storage and shelf-life on sensory quality and consumer acceptance of ‘Abate Fetel’ pears

Fruit products certified by quality labels should guarantee high levels of consumer acceptance, despite the unavoidable variability arising from growing conditions and postharvest responses. The quality of ‘Abate Fetel’ pear (Pyrus communis L.) fruit was studied, after short or long cold storage, by analysis of physicochemical, texture and flavour traits, to investigate factors affecting consumer acceptance. Fruit from three orchards differing in location and design, monitored during 10 d of ripening at 20 °C, softened progressively to reach and exceed firmness adequate for consumption. Change in colour, in particular hue angle, paralleled softening. Sensory traits were investigated by evaluating fruit of three different firmness levels within the range of acceptable eating quality. Firmness differences were clearly perceived both by expert judges and by consumers, but did not influence the degree of liking. ‘Abate Fetel’ pear can maintain acceptable eating quality at 20 °C for 4–8 d after 13 weeks storage at ?1 °C, or 2–6 d after 23 weeks storage at ?1 °C. Changing texture parameters were perceived at eating, without compromising overall quality. Production system affected intrinsic quality parameters such as total soluble solids concentration, but did not influence consumer acceptance. In consumer tests conducted after 13 weeks of cold storage, high scores were recorded, with a 86% acceptance frequency and more than 40% of scores reflecting “like very much” or “like extremely”. After 23 weeks of cold storage a decrease in degree of liking was observed. The overall value of ‘Abate Fetel IGP Emilia-Romagna’ quality label was confirmed by consumer evaluations. However, the decrease in consumer acceptance after 23 weeks of cold storage indicates that caution should be used in using long storage durations.     

Targeted metabolomics study of ‘Braeburn’ apples during long-term storage

‘Braeburn’ is an apple cultivar susceptible to the occurrence of internal browning (Braeburn Browning Disorder; BBD) during storage. This physiological disorder is characterized by the development of brown spots inside the fruit, eventually resulting in the formation of cavities. The objective of this study was to investigate the effects of the preharvest application of calcium, potassium and triazole fungicides on the postharvest primary metabolites of ‘Braeburn’ fruit, and to offer a better understanding of the biochemical processes behind internal browning. The primary metabolites of ‘Braeburn’ fruit cortex samples at harvest and after 2 weeks, 4 weeks, 4 months and 8 months of storage at browning-inducing conditions were analyzed using GC–MS. No significant difference in the primary metabolites was observed between the different levels of the applied preharvest applications. Early during storage, fruit developed browning, with the severity increasing with storage duration. This was correlated with a group of primary metabolites that showed either an increase (e.g., alanine, galactose, mannitol, sorbitol, xylose) or a decrease (e.g., malate, sucrose) in concentration with time. Radial distribution of the metabolites in the fruit tissue was also observed; some metabolites (e.g., galactose, mannitol) were higher in concentration in the inner cortex, while the concentrations of other metabolites (e.g., mannose, sucrose) were higher in the outer cortex.     

Physiological response of ‘Larry Ann’ plums to cold storage and 1-MCP treatment

The aim of this work was to study the specific effects of low temperature and 1-MCP treatment on ethylene metabolism and oxidative behaviour in plums (Prunus × salicina cv. Larry Ann). Control fruit were stored at 20 °C or 0 °C and the 1-MCP (625 nL L^?1) treated fruit at 0 °C. Changes in the kinetics of ethylene production upon removal were related to changes in ACC metabolism (ACC and MACC levels), oxidative behaviour (H₂O₂ content) and enzymatic antioxidant potential (SOD, CAT and POX enzymes) during cold storage. Low temperature stress inhibited the synthesis of MACC, which appeared to be the basic process that regulated ACC and ethylene production at ambient temperature. Although 1-MCP treatment inhibited ethylene production and ACC accumulation in the cold, it did not inhibit the accumulation of MACC. Neither cold nor 1-MCP treatment induced oxidative stress. Nevertheless, the 1-MCP treatment significantly impaired the increase in POX activity observed during cold storage. Collectively these results showed the underlying role that ACC metabolism plays in the ripening behaviour of cold-stored plums, confirming previous results. The results also indicate that MACC and malonyl transferase activity are the key regulatory factors that control ripening and possibly some ethylene-related disorders such as chilling injury in cold-stored plums.     

Biochemical and proteomic analysis of ‘Kyoho’ grape (Vitis labruscana) berries during cold storage

Low temperature storage is widely used to maintain the quality of postharvest fruit and extend their shelf-life. In this study, changes in specific metabolites and protein expression profiles of grape berries under cold storage were investigated by liquid chromatography and proteomic studies, respectively. During cold storage, total soluble solids and reducing sugars accumulation was accompanied by a decline in organic acids and phenols contents. A comparative analysis of the proteomes of grape berries during cold storage was performed using a two-dimensional electrophoresis (2-DE) proteomic approach. Seventy-nine differentially regulated proteins during cold storage were successfully identified by matrix-assisted laser desorption/ionization time of flight (MALDI-TOF) mass spectrometry, and classified into eight main categories based on their biological function. Down-regulation of proteins associated with glycolysis and the Krebs cycle, and up-regulation of cell wall polysaccharide degradation-related enzymes provided molecular evidence that soluble sugar and carbohydrate metabolism play a crucial role in postharvest regulation. In addition, cold storage increased the expression abundance of several stress related proteins such as heat shock proteins, proteasome and antioxidant enzymes, suggesting a physiological adaptation to low temperature was induced in grape berries. This study contributes to a better understanding of the cellular events in grape berries under cold storage and provides potentially useful information for maintaining fruit quality and minimizing postharvest losses.     

Correlation and path-coefficient analyses of ripening attributes and storage disorders in ‘Ambrosia’ and ‘Empire’ apples

The objectives of this study were: (1) to determine correlation effects among the ripening attributes of ‘Empire’ and ‘Ambrosia’ apples during storage, and (2) to determine the direct and indirect contributions of these ripening attributes on the incidence of physiological disorders and storage rots using path-coefficient analysis. The analysis was applied to data obtained from a variety of harvest dates and storage regimes from apples. Pearson correlation analysis of the data indicated a strong positive correlation between internal ethylene concentration (IEC) and peel greasiness, a negative correlation between IEC and soluble solids concentration, and a negative correlation between firmness and peel greasiness in both cultivars, as well as a negative correlation between IEC and firmness in ‘Empire’. Results indicated that increased IEC in ‘Ambrosia’ apples during storage was related to higher incidences of core browning and lenticel damage and lower incidence of internal browning. Higher IEC in ‘Empire’ apples during storage was associated with less internal browning. Several significant correlations, representing different relationships among the ripening attributes and storage disorders were obtained.     

Low dose gamma irradiation does not affect the quality,proximate or nutritional profile of ‘Brigitta’ blueberry and ‘Maravilla’ raspberry fruit

Blueberry (Northern Highbush, cv ‘Brigitta’) and raspberry (cv ‘Maravilla’) fruit were subject to low dose gamma irradiation (0, 150, 400 and 1000 Gy) and stored at 0 °C for three or ten days (blueberry) and two or seven days (raspberry) to determine the effects of irradiation on fruit quality and nutritional and proximate contents. In general, none of the irradiation doses (≤1000 Gy) significantly affected blueberry or raspberry fruit quality (overall fruit quality, colour, firmness, weight loss, TSS, TA levels or TSS/TA ratio), or the nutritional or proximate content (ash, carbohydrate, dietary fibre, energy, moisture, protein, sodium, potassium, total sugars, fructose, ascorbic acid, monomeric anthocyanin, citric and malic acids). The length of time in storage affected some fruit quality and nutritional and proximate content parameters (such as overall fruit quality, firmness, weight loss, TA levels, dietary fibre, potassium, ascorbic acid, citric and malic acids), with longer storage periods resulting in lower quality fruit, irrespective of irradiation treatment. No interaction was detected between the effects of irradiation treatment and storage time, indicating that the storage effect was consistent for all irradiation doses on both blueberry and raspberry fruit quality.     

Maturity and cooling rate affects browning,polyphenol oxidase activity and gene expression of ‘Yali’ pears during storage

Browning is the main physiological disorder of ‘Yali’ pear (Pyrus bretschneideri Rehd) during storage. In this study, the relationships between browning development in fruit from different harvest dates, and cooled either rapidly or slowly, with polyphenol oxidase (PPO) activity and isozymes, and PPO gene expression has been investigated. Development of browning was highest in late-harvest fruit in both core and flesh tissues and was higher in rapidly cooled than slowly cooled fruit. Mid-harvest fruit had the lowest browning incidence and PPO activity of core tissue was higher than in flesh and seeds, while the peak of PPO activity in mid-harvest fruit was the lowest. Six PPO isoenzymes were detected in fruit, three bands A, B and E in flesh and core tissues, three bands C, D and F in the seeds. The intensity of PPO isoenzyme staining of bands A and B in pulp and core was similar to that of PPO activity and browning incidence. PPO gene expression increased and then decreased in core tissues. Trends of expression were similar to those of PPO activity. Rapid cooling promoted the expression PPO. The results suggest PPO plays an important role in ‘Yali’ pear browning during storage.     

Effect of 60Coγ-irradiation doses on nutrients and sensory quality of fresh walnuts during storage

Fresh Liaohe walnuts (Juglans regia cv. Liaoning4) were given ⁶⁰Coγ-irradiation doses of 0, 0.1, 0.5, 1.0 and 5.0 kGy and stored at 0 ± 1 °C for 120 d. The concentrations of fat, protein, fatty acid, soluble sugar, water and vitamin E (V_E), peroxide value (PV) and the sensory quality were determined at regular intervals during storage. Irradiation at 0.1, 1.0 and 5.0 kGy accelerated lipid oxidation, increased the PV, and decreased the sensory quality and V_E content of walnuts during storage. However, an irradiation dose of 0.5 kGy resulted in less oxidative degradation, reduced PV, and maintained a higher V_E concentration and better sensory quality of walnuts during the 90 d storage. We conclude that a dose of 0.5 kGy is the optimal dose for the preservation of fresh walnuts over a 90 d storage period.     

Use of chlorine dioxide fumigation to alleviate enzymatic browning of harvested ‘Daw’ longan pericarp during storage under ambient conditions

Pericarp browning reduces both the shelf-life and market value of harvested longan fruit stored at room temperature. Our study investigated the efficiency of chlorine dioxide (ClO₂) fumigation at reducing pericarp browning of longan (Dimocarpus longan Lour.) cv. Daw. Fresh longan fruit were fumigated with 0 (control), 2.5, 5, 10 and 25 mg/L ClO₂ for 10 min, before being packed in cardboard boxes, and stored at 25 ± 1 °C, RH 82 ± 5% for 7 days. Fruit treated with ClO₂ had a lower browning index, but higher hue angle (true color), L* (lightness) and b* (yellowness) values than non-treated fruit. The 10 and 25 mg/L ClO₂ treatments were the most effective at extending shelf-life from 1 to 5 days, compared with the control, by reducing pericarp browning, the activities of polyphenol oxidase (PPO) and peroxidase (POD), disease development and by maintaining the highest total phenolic content. However, quality acceptance of fruit treated with 10 mg/L ClO₂ was higher than fruits treated with 25 mg/L, as determined by odor and flavor. Consequently, ClO₂ fumigation at a concentration of 10 mg/L was considered to be the most effective treatment to reduce pericarp browning of longan, whilst maintaining fruit quality.     

Characterization of ethylene biosynthesis and its regulation during fruit ripening in kiwifruit,Actinidia chinensis ‘Sanuki Gold’

Ethylene biosynthesis in kiwifruit, Actinidia chinensis ‘Sanuki Gold’ was characterized using propylene, an ethylene analog, and 1-methylcyclopropene (1-MCP), an inhibitor of ethylene perception. In fruit harvested between a young stage (66 days after pollination) (DAP) and an early commercial harvesting stage (143 DAP), 2 days of exposure to propylene were sufficient to initiate ethylene biosynthesis while in fruit harvested at commercial harvesting stage (154 DAP), 4 days of propylene treatment were required. This observation suggests that response of ethylene biosynthesis to propylene treatment in kiwifruit declined with fruit maturity. Propylene treatment resulted in up-regulated expression of AC-ACO1, AC-ACO2, AC-SAM1 and AC-SAM2, prior to the induction of AC-ACS1 and ethylene production, confirming that AC-ACS1 is the rate limiting step in ethylene biosynthesis in kiwifruit. Treatment of fruit with more than 5 μL L^?1 of 1-MCP after the induction of ethylene production subsequently suppressed ethylene production and expression of ethylene biosynthesis genes. Treatment of fruit with 1-MCP at harvest followed with propylene treatment delayed the induction of ethylene production and AC-ACS1 expression for 5 days. These observations suggest that in ripening kiwifruit, ethylene biosynthesis is regulated by positive feedback mechanism and that 1-MCP treatment at harvest effectively delays ethylene production by 5 days.