Controlled atmosphere storage of guava (Psidium guajava L.) fruit

The effects of controlled atmospheres (CA) on respiration, ethylene production, firmness, weight loss, quality, chilling injury, and decay incidence of three commercially important cultivars of guava fruit were studied during storage in atmospheres containing 2.5, 5, 8, and 10 kPa O₂ with 2.5, 5, and 10 kPa CO₂ (balance N₂) at 8 °C, a temperature normally inducing chilling injury. Mature light green fruit of cultivars, ‘Lucknow-49’, ‘Allahabad Safeda’ and ‘Apple Colour’, were stored for 30 days either in CA or normal air, and transferred to ambient conditions (25–28 °C and 60–70% R.H.) for ripening. CA storage delayed and suppressed respiratory and ethylene peaks during ripening. A greater suppression of respiration and ethylene production was observed in fruit stored in low O₂ (≤5 kPa) atmospheres compared to those stored in CA containing 8 or 10 kPa O₂ levels. High CO₂ (>5 kPa) was not beneficial, causing a reduction in ascorbic acid levels. CA storage was effective in reducing weight loss, and maintaining firmness of fruit. The changes in soluble solids content (SSC), titratable acidity (TA), ascorbic acid, and total phenols were retarded by CA, the extent of which was dependent upon cultivar and atmosphere composition. Higher amounts of fermentative metabolites, ethanol and acetaldehyde, accumulated in fruit held in atmospheres containing 2.5 kPa O₂. Chilling injury and decay incidence were reduced during ripening of fruit stored in optimal atmospheres compared to air-stored fruit. In conclusion, guava cultivars, ‘Lucknow-49’, ‘Allahabad Safeda’, and ‘Apple Colour’ may be stored for 30 days at low temperature (8 °C) supplemented with 5 kPa O₂ + 2.5 kPa CO₂, 5 kPa O₂ + 5 kPa CO₂, and 8 kPa O₂ + 5 kPa CO₂, respectively.     

Influence of the combination of different atmospheres on diphenylamine,folpet and imazalil content in cold-stored ‘Pink Lady®’ apples

‘Pink Lady^®’ apples were harvested at commercial maturity, treated with three different agrochemical products, and stored at 1 °C under either air or controlled atmosphere conditions (2 kPa O₂ + 2 kPa CO₂ and 1 kPa O₂ + 1 kPa CO₂) for 13 and 27 weeks, followed by 4 weeks storage in air at 1 °C. Diphenylamine, folpet and imazalil contents in both the skin and flesh were simultaneously determined after cold storage plus simulated marketing periods of 1 and 7 d at 20 °C. After 27 weeks plus 7 d, diphenylamine and folpet levels in apple skin were lower for fruit stored in low O₂ (2 kPa) or air than for those kept under ultra-low O₂ (1 kPa). An additional storage period of 4 weeks in air reduced diphenylamine and folpet contents in whole apples stored for 13 weeks in the low O₂ controlled atmosphere. For imazalil, the same result was obtained in apple skins stored for 27 weeks under an ultra-low O₂ controlled atmosphere. Differences in diphenylamine and folpet contents were found for skin and flesh samples throughout the simulated marketing period, but there were observable differences in imazalil contents only for flesh samples.     

Relationships between the instrumental and sensory characteristics of four peach and nectarine cultivars stored under air and CA atmospheres

‘Big Top’ and ‘Venus’ nectarines and ‘Early Rich’ and ‘Sweet Dream’ peaches were picked at commercial maturity and stored for 20 and 40 d at −0.5 °C and 92% RH under either air or one of the three different controlled atmosphere regimes (2 kPa O₂/5 kPa CO₂, 3 kPa O₂/10 kPa CO₂ and 6 kPa O₂/17 kPa CO₂). Physicochemical parameters and volatile compounds emission were instrumentally measured after cold storage plus 0 or 3 d at 20 °C. Eight sensory attributes were assessed after cold storage plus 3 d at 20 °C by a panel of 9 trained judges, in order to determine the relationship between sensory and instrumental parameters and the influence of storage period and cold storage atmosphere composition on this relationship.A principal component analysis (PCA) was undertaken to characterize the samples according to their sensory attributes. PCA results reflected the main characteristics of the cultivars: ‘Big Top’ was the nectarine cultivar with the highest values for sweetness, juiciness and flavor; ‘Sweet Dream’ was the sweetest peach and was characterized by high values for crispness and firmness, while ‘Venus’ and ‘Early Rich’ were characterized by their sourness. To assess the influence of storage period and CA composition on sensory properties, a PLS model of the flavor of the different samples was constructed using standard quality attributes and volatile concentrations as the X-variables. The model with 2 factors accounted for more than 80% of flavor variance. PLS results indicated that the main influence on flavor perception was storage period. Atmosphere composition also had an influence on flavor perception: flavor perception decreased from samples stored in a 2/5 O₂/CO₂ atmosphere composition to those of 3/10 and 6/17. These results can be qualitatively extended to juiciness and sweetness since all these sensory properties were strongly correlated.     

Pithy brown core in ‘d’Anjou’ pear (Pyrus communis L.) fruit developing during controlled atmosphere storage at pO2 determined by monitoring chlorophyll fluorescence

Physiological responses and fruit quality of ‘d’Anjou’ pear fruit from five orchard lots were evaluated after cold storage in air or controlled atmospheres (CA) with the O₂ concentration based on assessment of fruit chlorophyll fluorescence (CF) or standard conditions (1.5 kPa O₂). The pCO₂ for all CA fruit was 0.5 kPa. Softening, acid loss, and peel degreening of all lots were delayed at one or more evaluation dates (2, 4, 6, 8 months) by previous storage at the CF pO₂ compared with fruit stored in 1.5 kPa O₂ or in air. Superficial scald developed on fruit previously stored in air but not on fruit stored in a CA. Pithy brown core developed on fruit from all lots stored at the CF pO₂ and on fruit stored at 1.5 kPa in 3 of the 5 lots. Pithy brown core incidence decreased with advanced harvest maturity. Post-storage ethylene and CO₂ production were in most instances lowest for fruit stored at the CF pO₂. A significant relationship between fruit ethanol content and pithy brown core incidence was observed. Results indicate low pO₂ storage based on CF monitoring slows fruit ripening relative to fruit stored at 1.5 kPa O₂, prevents superficial scald development compared with fruit stored in air, however, development of pithy brown core in fruit stored at the CF pO₂ was not accompanied by a change in CF.     

Responses of 1-MCP application in plums stored under air and controlled atmospheres

The potential of 1-MCP for controlling ripening in ‘Angeleno’ plum fruit under air and controlled atmosphere (CA) storage was explored, and the possibility that 1-MCP can inhibit development of brown rot caused by Monilinia laxa and internal breakdown in ‘Fortune’ and ‘Angeleno’ plums tested. After harvest, fruit were exposed to 300 and 500 nl l⁻¹ (in 2003) and 500 nl l⁻¹ 1-MCP (in 2004) at low temperatures (0–3 °C) for 24 h. After treatment the plums were stored in air at 0 °C and ‘Angeleno’ fruit were also stored in CA storage (1.8% O₂ + 2.5% CO₂). Following storage, fruit were kept at 20 °C. In ‘Angeleno’ fruit, 1-MCP was effective in delaying the loss of firmness and colour changes during holding at 20 °C. 1-MCP reduced brown rot in fruit stored in CA but no significant reduction was found in air storage. Internal breakdown, a major physiological storage disorder in plums, was inhibited by 1-MCP treatment. Furthermore, since 1-MCP applied in air storage showed better results than the control in CA conditions, an application of 1-MCP before air storage could be the best way to reduce the ripening process for short or medium storage periods (40 and 60 days). CA storage plus 1-MCP treatment could be used for long periods (80 days).     

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.     

Physicochemical measurements in ‘Mondial Gala®’ apples stored at different atmospheres: Influence on consumer acceptability

Standard quality parameters, consumer acceptability, emission of volatile compounds and ethylene production of ‘Mondial Gala^®’ apples (Malus × domestica Borkh.) were determined in relation to storage atmosphere, storage period and shelf-life period. Fruit were harvested at the commercial date and stored in AIR (21 kPa O₂:0.03 kPa CO₂) or under three different controlled atmospheres (CAs): LO (2 kPa O₂:2 kPa CO₂), ULO1 (1 kPa O₂:1 kPa CO₂), or ULO2 (1 kPa O₂:2 kPa CO₂). Fruit samples were analysed after 12 and 26 weeks of storage plus 1 or 7 d at 20 °C.Apples stored in CA maintained better standard quality parameters than AIR-stored fruit. The volatile compounds that contributed most to the characteristic aroma of ‘Mondial Gala^®’ apples after storage were butyl, hexyl and 2-methylbutyl acetate, hexyl propanoate, ethyl butanoate, ethyl hexanoate, ethyl, butyl and hexyl 2-methylbutanoate. Data obtained from fruit analysis were subjected to principal component analysis (PCA). The apples most accepted by consumers showed the highest emission of ethyl 2-methylbutanoate, ethyl hexanoate, tert-butyl propanoate and ethyl acetate, in addition to the highest titratable acidity and firmness values.     

Postharvest life and flavor quality of three strawberry cultivars kept at 5 °C in air or air+20 kPa CO2

The postharvest life and flavor quality of three strawberry (Fragaria x ananassa D.) cultivars (Aromas, Diamante and Selva) kept at 5 °C in air or air+20 kPa CO₂ for up to 15 days were investigated. ‘Diamante’ and ‘Selva’ had better flavor quality than ‘Aromas’ strawberries, as indicated by levels of titratable acidity and total soluble solids, organic acids, sugars and some aroma compounds and by a consumer preference test. Flesh firmness was maintained in ‘Aromas’ and increased in ‘Diamante’ and ‘Selva’ strawberries during storage at 5 °C in both air and air+20 kPa CO₂. Fruit color was not affected by CO₂ treatments. The postharvest life based on appearance was 7, 9 and 9 days for ‘Aromas’, ‘Diamante’ and ‘Selva’ fruits stored in air and it was extended by 2, 2 and 4 days, respectively, by the CO₂-enriched atmosphere. However, the level and proportion of flavor components (sugars, organic acids, aroma compounds) and fermentative metabolites, as well as the results of sensory evaluations, indicated that the flavor life was shorter than postharvest life based on appearance in ‘Aromas’ fruit stored in air (5 vs. 7 days) and in CO₂-stored ‘Aromas’ (7 vs. 9 days) and ‘Selva’ (11 vs. 13 days) fruit. ‘Selva’ and ‘Diamante’ strawberries retained their flavor quality during storage at 5 °C in air for 9 days and CO₂-stored ‘Diamante’ fruit for 11 days.     

Interaction of temperature control deficiencies and atmosphere conditions during blueberry storage on quality outcomes

Southern hemisphere blueberry producers often export their products through extended supply chains to Northern hemisphere consumers. During extended storage, small variations in temperature or atmosphere concentrations may generate significant differences in final product quality. In addition, relatively short delays in establishing cool storage temperatures may contribute to quality loss. In these experiments a full factorial analysis was done of the effects of three cooling delays (0, 12 or 24 h at 10 °C), three atmosphere concentrations (air, 10% CO₂ + 2.5% O₂ and 10% CO₂ + 20% O₂) and two storage temperatures (0 °C and 4 °C) which were assessed for their impact on final quality, measured as weight loss, firmness and rot incidence. Two blueberry cultivars were studied: ‘Brigitta’, a highbush cultivar, and ‘Maru’, a rabbiteye. Delays in cooling had a small effect on final product weight, whereas variation in storage temperature and atmosphere during simulated transport influenced both firmness and rot incidence. Atmospheres with 10% CO₂ reduced decay incidence, particularly at low oxygen concentration (2.5% O₂), although the latter conditions tended to soften fruit. In order to achieve optimal postharvest storage for blueberries, minimising temperature variability in the supply chain is important, as is finding the potentially cultivar-specific optimal combination of high CO₂ and low O₂ concentration that results in simultaneously minimising rot incidence and induced softening.     

Control of blue mold of apple by combining controlled atmosphere,an antagonist mixture,and sodium bicarbonate

‘Golden Delicious’ apples were wound-inoculated with Penicillium expansum and treated with various combinations of sodium bicarbonate and two antagonists (Metschnikowia pulcherrima, Cryptococcus laurentii), and then stored in air or controlled atmosphere (CA = 1.4 kPa O₂ and 3 kPa CO₂) for 2 or 4 months at 1 °C. The antagonists survived and their populations increased during both air and CA storage. The antagonists alone reduced blue mold but were more effective when combined. Sodium bicarbonate tended to reduce lesion size when used with these antagonist, either when they were used alone or combined. Storage under CA conditions also increased the effectiveness of both antagonist, when used alone or in combination. The only treatment that completely eliminated P. expansum-incited decay was the combination of the two antagonists and sodium bicarbonate on fruit stored under CA conditions. The proper combination of alternative control measures can provide commercially acceptable long-term control of fruit decay and could help reduce our dependency on fungicides.     

Impact of atmospheric ozone-enrichment on quality-related attributes of tomato fruit

Tomato fruit (Lycopersicon esculentum L. cv. Carousel) were exposed to ozone concentrations ranging between 0.005 (controls) and 1.0 μmol mol⁻¹ at 13 °C and 95% RH. Quality-related attributes and organoleptic characteristics were examined during and following ozone treatment. Levels of soluble sugars (glucose, fructose) were maintained in ozone-treated fruit following transfer to ‘clean air’, and a transient increase in β-carotene, lutein and lycopene content was observed in ozone-treated fruit, though the effect was not sustained. Ozone-enrichment also maintained fruit firmness in comparison with fruit stored in ‘clean air’. Ozone-treatment did not affect fruit weight loss, antioxidant status, CO₂/H₂O exchange, ethylene production or organic acid, vitamin C (pulp and seed) and total phenolic content. Panel trials (employing choice tests, based on both appearance and sensory evaluation) revealed an overwhelming preference for fruit subject to low-level ozone-enrichment (0.15 μmol mol⁻¹), with the effect persisting following packaging.     

Effect of cold storage on vitamin C,phenolics and antioxidant activity of five orange genotypes [Citrus sinensis (L.) Osbeck]

The effect of cold storage on antioxidant profile and the antioxidant activity of five sweet orange genotypes [Citrus sinensis (L.) Osbeck], three blood (pigmented) varieties with different anthocyanin contents (‘Tarocco Messina’, ‘Tarocco Meli’ and ‘Moro’) and two blond varieties (‘Ovale’ and ‘Valencia late’), stored at 6 ± 1 °C for 65 d was investigated. During fruit storage, anthocyanins, hydroxycinnamic acids, vitamin C, flavanones and total phenolics were determined, and juice antioxidant capacity was measured by two different in vitro tests (DPPH scavenging activity and inhibition of induced linoleic acid peroxidation). The results showed an increase in anthocyanins, flavanones and hydroxycinnamic acids and a slight decrease in vitamin C in the blood oranges. Cold storage negatively affected flavanone concentration, while positively influenced vitamin C in blond orange varieties. Both antioxidant activity tests showed an increase in antioxidant capacity during storage caused mainly by phenolic accumulation (blood oranges) and vitamin C increase (blond oranges). Finally, correlations between antioxidant activity and total or individual phenolic components were examined.     

Combination of postharvest antifungal chemical treatments and controlled atmosphere storage to control gray mold and improve storability of ‘Wonderful’ pomegranates

Common food additives (sodium bicarbonate (SB), sodium carbonate (SC), and potassium sorbate (PS)) were compared to the fungicide fludioxonil for the control of gray mold on California-grown ‘Wonderful’ pomegranates artificially inoculated with Botrytis cinerea and stored at 7.2 °C in either air or controlled atmosphere (CA, 5 kPa O₂ + 15 kPa CO₂) conditions. Fludioxonil was superior to other treatments. PS was the most effective additive. Synergistic effects between antifungal treatments and CA storage were observed. After 15 weeks of storage at 7.2 °C, the combination of PS treatment (3 min dip in 3% solution at 21 °C) and CA storage was as effective as the combination of heated fludioxonil (30 s dip in 0.6 g L⁻¹ of active ingredient at 49 °C) and air storage. Mixtures of PS with SB or SC did not improve the efficacy of either treatment alone. In tests conducted in commercial facilities, decay development and external and internal fruit quality were assessed on naturally infected pomegranates stored in either air or CA after application of a selected postharvest antifungal combined treatment (CTrt) integrating PS, SB + chlorine, and fludioxonil. CTrt was effective in controlling natural gray mold after 6 weeks of storage at 8.9 °C, but lacked persistence and it was not effective after 14 weeks. CA storage greatly enhanced decay control ability of CTrt. Skin red color was better maintained in CA-stored than in air-stored fruit. Juice color and properties (SSC, TA, and pH) were not practically affected by either postharvest treatment or storage condition. The integration of PS treatments with CA storage could provide an alternative to synthetic fungicides for the management of pomegranate postharvest decay.     

Changes in postharvest physicochemical and sensory characteristics of hardy kiwifruit (Actinidia arguta and its hybrid) after cold storage under normal versus controlled atmosphere

Changes in sensory and physicochemical characteristics of fruit of Actinidia arguta and its hybrid after cold storage (1 °C and 85%RH) in air (AS) versus controlled atmosphere (CA) with low oxygen concentration (1.5%O₂ + 1.5%CO₂) were examined over a period of four and eight weeks. The investigation was carried out on two cultivars, ‘Ananasnaya’ (A. arguta) and ‘Bingo’ (Actinidia purpurea × A. arguta) harvested at two stages of maturity (6.5–8% and 8–9.5% soluble solids, respectively). During long-term storage the strongest changes in fruit characteristics were in fruit firmness and acidity. Air storage was an adequate method of refrigerated storage of fruit over a short period of 4 weeks. Application of CA can be very useful for storing hardy kiwifruit over a longer, 8 week period. The sensory characteristics of fruit stored in CA and then ripened during simulated shelf-life were similar to those of vine ripe fruit. The most significant negative change in the sensory characteristics of fruit after long-term cold storage was the increase in the intensity of their bitter taste.     

Multivariate analysis of modifications in biosynthesis of volatile compounds after CA storage of ‘Fuji’ apples

Emission of aroma volatile compounds and some related enzyme activities (LOX, PDC, ADH, and AAT) were assessed in ‘Fuji’ apples (Malus × domestica Borkh.) during shelf life at 20 °C following cold storage under air or under three different CA conditions (3 kPa O₂:2 kPa CO₂; 1 kPa O₂:1 kPa CO₂; or 1 kPa O₂:2 kPa CO₂). Data were used for principal component analysis (PCA) and partial least-square regression (PLSR) analysis of results. LOX activity was partly inhibited by hypoxic conditions, and thus could have contributed to differentiation between air- and CA-stored fruit. Accordingly, emission of straight-chain esters was also higher in air- than in CA-stored fruit. In contrast, PDC activity was responsible for part of the differences between low (3 kPa) and ultra-low (1 kPa) O₂ storage conditions, probably by providing substrates for AAT action. AAT activity afforded no satisfactory differentiation between samples, and therefore it is suggested that substrate availability is a more decisive factor than enzyme activity for volatile production after storage. The PCA and PLSR models developed in this work were not useful for discrimination between the two studied ultra-low O₂ conditions.     

Shrivel development in kiwifruit

Shrivel is a potential storage quality problem for kiwifruit. ‘Zesy003’ (commonly called Gold9) is a newly released, yellow-fleshed Actinidia chinensis cultivar that tends to shrivel more than other commercialised cultivars. Water loss and shrivel in Gold9 fruit were investigated during storage at 1 °C for up to 14 weeks and shelf-life at 20 °C. In addition, the water status of ripe fruit was quantified by magnetic resonance imaging and the capacity of a crude outer pericarp cell wall extract to swell. Shrivelled Gold9 fruit had 1–6% weight loss, although 6% weight loss did not always result in shrivel. Three weeks of storage resulted in fruit taking longer to shrivel during shelf-life, with a concomitant higher weight loss by the time the fruit was shrivelled. In contrast, 14 weeks of storage resulted in fruit that shrivelled more rapidly in shelf-life at a lower weight loss. At any given time after harvest, fruit with more severe shrivel tended to be softer than less shrivelled fruit. Shrivel therefore appears associated with fruit softening. Outer pericarp tissue from ripe Gold9 fruit had lower water mobility and a greater capacity to swell than pericarp from other kiwifruit cultivars. It is concluded that shrivel is not determined simply by an absolute amount of water loss. The development and ease of expression of shrivel in Gold9, and possibly other kiwifruit, is influenced by softening and the water characteristics of the fruit outer pericarp when soft.     

Modified ethanol atmosphere to control decay of table grapes during storage

The efficacy of three methods of applying ethanol to prevent storage decay was tested on two cultivars of table grapes, ‘Superior’ and ‘Thompson Seedless’. Ethanol was applied by: (1) dipping grapes in 50% ethanol for 10 s followed by air drying before packaging; (2) placing a container with a wick and 4 or 8 ml ethanol/kg grapes inside the package; (3) applying 4 or 8 ml ethanol/kg grapes to paper and placing this paper above the grapes in the package. The grapes were stored for 6 or 8 weeks at 0 °C and assessed after an additional 3 days at 20 °C. All methods of application controlled decay as well as or better than a SO₂-releasing pad. The ethanol impregnated paper caused high levels of berry browning, perhaps because of high levels of acetaldehyde inside the package. However, the taste of the berries was not impaired by any of the ethanol applications. The taste of ‘Thompson Seedless’ grapes stored for 8 weeks in modified atmosphere storage was affected by CO₂ levels above 7%. Some methods of applying ethanol used here show promise as alternatives to SO₂ to prevent decay of grapes during storage while maintaining fruit quality.     

Extending the shelf life of fresh-cut eggplant with a soy protein–cysteine based edible coating and modified atmosphere packaging

The effect of a soy protein-based edible coating with antioxidant activity, and conventional and superatmospheric modified atmosphere (MA) packaging, on the quality of fresh-cut ‘Telma’ eggplants, was evaluated during storage. In a first experiment, eggplant pieces were dipped in either a coating composed of soy protein isolate (SPI) and 0.5% cysteine (Cys), or water as an uncoated control. Samples were packed in trays under atmospheric conditions to reach a passive MA (MA-P) or two gas mixtures (MA-A: 15 kPa CO₂ + 5 kPa O₂; MA-B: 80 kPa O₂) and were stored at 5 °C. Atmospheric conditions were used as the control conditions (Control). The coated samples packed under MA-B and Control conditions resulted in the highest whiteness index (WI) values during storage, whereas MA-A did not improve the shelf-life of minimally processed eggplants and had the lowest WI values. The MA-B and atmospheric control conditions helped to maintain firmness, whereas the coating helped to maintain the weight loss under MA-A and MA-B. The maximum commercial shelf-life was reached on day 6 for the coated samples packed under atmospheric conditions. In a second experiment, the commercial shelf-life of fresh-cut eggplants was extended to 8 and 9 storage days by increasing the Cys content in the edible coating from 0.5 to 1% under MA-B and Control storage conditions, respectively.     

Blueberry leaf extracts incorporated chitosan coatings for preserving postharvest quality of fresh blueberries

The phenolic compounds in blueberry (Vaccinium spp.) fruit and leaf extracts (BLE) were determined based on HPLC analysis. Antimicrobial assays against Staphylococcus aureus, Listeria monocytogenes, Salmonella typhimurium and Escherichia coli, as well as fungi isolated from the rotting blueberry fruit were conducted. The effects of chitosan coating incorporating different concentrations of BLE on the quality of fresh fruit during postharvest storage at 2 ± 1 °C and 95 ± 2% relative humidity (RH) for 35 d and then at room conditions for 3 d were also investigated. Five different coating treatments were applied including 2% (w/v) chitosan coating (T1), 2% (w/v) chitosan coating containing 4% (w/v, T2), 8% (w/v, T3), or 12% (w/v, T4) BLE, and 2% (w/v) chitosan coating containing 12% BLE plus modified atmosphere packaging (MAP at 3 kPa O₂ + 12 kPa CO₂) (T5). A sample of blueberries dipped into distilled water was used as control (T0). BLE had a greater variety of phenolic compounds than fruit extracts with syringic acid the highest concentration (0.259 ± 0.003 g kg⁻¹), but the total phenolic content in BLE was lower (P < 0.05) than in fruit extracts. BLE showed good antimicrobial activity against all tested microorganisms, with a minimum inhibition concentration from 25 to 50 g L⁻¹. The 2% chitosan coating that incorporated 8% or 12% BLE showed some degree of decreasing decay rate of fruit compared with the control, and the coating with BLE plus MAP had more effective control of fruit decay. All treated samples maintained higher total phenolic content and radical scavenging activity than the control. This study suggested that chitosan coating incorporating BLE can be employed to extend shelf-life and maintain high nutritional value of fresh blueberries during postharvest storage.     

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.