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).     

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.     

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.     

Effect of sustained deficit irrigation on physicochemical properties,bioactive compounds and postharvest life of pomegranate fruit (cv. ‘Mollar de Elche’)

In this study, the influence of sustained deficit irrigation (SDI; 32% of reference evapotranspiration (ET₀)) on physicochemical and sensory quality and bioactive compounds of pomegranates stored for 30, 60 and 90 days in air at 5 °C + 4 days at 15 °C, at each storage period, was studied and compared to a control (100% ET₀). Fruit from SDI had higher peel redness and greater firmness, soluble solids contents, vitamin C (27%), phloretin (98%) and protocatechuic acid (10%) levels, and total antioxidant capacity (TAC) (46%) than the control. Cold storage and shelf-life did not induce significant changes in soluble solids, pH, titratable acidity, and chroma and Hue. SDI fruit had retarded development of chilling injury (CI) symptoms, which appeared after 60 days of storage in comparison to 30 days in the controls. Anthocyanins, catechin, phloretin and protocatechuic, caffeic, p-coumaric and caffeic acids contents had greater increases in SDI fruit than in controls throughout the postharvest life. TAC was significantly (P < 0.05) correlated to anthocyanins, gallic acid and total vitamin C contents. Generally, after long term storage, the fruit grown under SDI showed higher sensory and nutritional quality, more health attributes and a longer shelf-life (up to 90 days at 5 °C + 4 at 15 °C) than fruit irrigated at 100% ET₀.     

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.     

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.     

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.     

Repeated treatment of apple fruit with 1-methylcyclopropene (1-MCP) prior to controlled atmosphere storage

The effect of multiple 1-MCP treatments prior to the establishment of controlled atmosphere (CA) storage on the quality of ‘McIntosh’ and ‘Empire’ apples [Malus × sylvestris (L.) Mill. var. domestica (Borkh.) Mansf.] was investigated. Fruit were harvested on three occasions over a 1 week period, and at each harvest cooled overnight and 1-MCP applied the following day. Fruit from the first or second harvests were treated again or for the first time when fruit from each successive harvest was treated. CA conditions were established after the last 1-MCP treatment and fruit were stored for up to 8 months. Delays in 1-MCP application generally resulted in progressively higher internal ethylene concentrations (IECs) at the time of treatment and lower firmness both at the time of treatment and after storage. Multiple 1-MCP applications kept IECs low and maintained firmness compared with single applications that were applied after 4 d. For ‘McIntosh’, external CO₂ injury was more prevalent after storage if fruit were treated without delays after harvest for earlier harvests while later harvests were less affected. For ‘Empire’, flesh browning was more prevalent in fruit from later harvests and 1-MCP treated fruit had higher levels than untreated fruit. Either early 1-MCP treatment or multiple treatments reduced senescent breakdown in ‘McIntosh’, and core browning and greasiness in ‘Empire’.     

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.     

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.     

Ethylene synthesis,ripening capacity,and superficial scald inhibition in 1-MCP treated ‘d’Anjou’ pears are affected by storage temperature

A continuing challenge for commercializing 1-methylcyclopropene (1-MCP) to extend the storage life and control superficial scald of ‘d’Anjou’ pear (Pyrus communis L.) is how to initiate ripening in 1-MCP treated fruit. ‘D’Anjou’ pears harvested at commercial and late maturity were treated with 1-MCP at 0.15 μL L⁻¹ and stored either at the commercial storage temperature −1.1 °C (1-MCP@−1.1 °C), or at 1.1 °C (1-MCP@1.1 °C) or 2.2 °C (1-MCP@2.2 °C) for 8 months. Control fruit stored at −1.1 °C ripened and developed significant scald within 7 d at 20 °C following 3–5 months of storage. While 1-MCP@−1.1 °C fruit did not develop ripening capacity due to extremely low internal ethylene concentration (IEC) and ethylene production rate for 8 months, 1-MCP@1.1 °C fruit produced significant amounts of IEC during storage and developed ripening capacity with relatively low levels of scald within 7 d at 20 °C following 6–8 months of storage. 1-MCP@2.2 °C fruit lost quality quickly during storage. Compared to the control, the expression of ethylene synthesis (PcACS1, PcACO1) and signal (PcETR1, PcETR2) genes was stable at extremely low levels in 1-MCP@−1.1 °C fruit. In contrast, they increased expression after 4 or 5 months of storage in 1-MCP@1.1 °C fruit. Other genes (PcCTR1, PcACS2, PcACS4 and PcACS5) remained at very low expression regardless of fruit capacity to ripen. A storage temperature of 1.1 °C can facilitate initiation of ripening capacity in 1-MCP treated ‘d’Anjou’ pears with relatively low scald incidence following 6–8 months storage through recovering the expression of certain ethylene synthesis and signal genes.     

Modified atmosphere packaging for extending the storage life of ‘Fuyu’ persimmon

Persimmon production in Brazil is concentrated from February to June. The large amount of this fruit available in the market influences its price during this period. This study was carried out to evaluate the effect of different packaging plastic materials on extending the storage life of ‘Fuyu’ persimmons kept under refrigeration. ‘Fuyu’ persimmon fruits were harvested on the mature-green stage and enclosed in groups of three (750 ± 30 g) in different packaging materials: 58-μm multilayer polyolephynic film (PO); 50-μm low density polyethylene film (LDPE) and 38-μm microperforated PO. Unpacked fruit stored in corrugated cardboard boxes were used as control. Fruit were stored at 1 ± 1 °C/90 ± 5% RH for 90 d. Every 7 d, five replicates of each treatment were evaluated for headspace gas composition (O₂, CO₂) and then transferred to 25 ± 1 °C/70 ± 5% RH for five more days. Then they were evaluated as to headspace gas composition (O₂, CO₂, acetaldehyde and ethanol), firmness, weight loss, skin and flesh color, total soluble solids, titratable acidity, pH, decay, discoloration and sensory attributes. The gas composition in the steady-state established in the 58-μm PO and 50-μm LDPE films extended the storage period up to 84 d at 1 °C plus 5 d at 25 °C differing significantly (P ≤ 0.05) from the control fruit as well as from those in the 38-μm microperforated PO, which were stored for 21 and 28 d, respectively. Off-flavors were not detected by sensory analysis. These results suggest that the 58-μm PO and 50-μm LDPE films are suitable for atmosphere modification and packaging of ‘Fuyu’ persimmon fruit stored under refrigeration with an additional period of time at ambient temperature.     

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.     

Role of putrescine in regulating fruit softening and antioxidative enzyme systems in ‘Samar Bahisht Chaunsa’ mango

The role of putrescine (PUT) in regulating fruit softening, antioxidative enzymes and biochemical changes in fruit quality was investigated during ripening and cold storage of mango (Mangifera indica cv. Samar Bahisht Chaunsa). Fruit were treated with various PUT concentrations (0.0, 0.1, 1.0 and 2.0 mM) and were allowed to ripen at 32 ± 2 °C for 7 days, or stored at 11 ± 1 °C for up to 28 days. Respiration rate and ethylene production were measured daily during ripening and cold storage. Cell wall degrading enzymes such as exo-polygalacturonase (exo-PG), endo-polygalacturonase (endo-PG), pectin esterase (PE), endo-1,4-β-d-glucanase (EGase), antioxidative enzymes including superoxide dismutase (SOD), peroxidase (POX), and catalase (CAT), fruit firmness as well as biochemical fruit quality characteristics were estimated during ripening and cold storage at 2 and 7 day intervals, respectively. PUT treatments reduced respiration rate, ethylene production and maintained higher fruit firmness during ripening as well as cold storage. PUT-treated fruit exhibited significantly suppressed activities of cell wall enzymes (exo-, endo-PG and EGase), but retained higher PE activity during ripening and cold storage. Total phenolic and antioxidant contents were significantly higher in PUT-treated fruit during ripening as well in the cold storage period than in the controls. Activities of antioxidative enzymes (CAT, POX and SOD) were also significantly higher in PUT-treated fruit during ripening as well as cold storage. SSC and SSC:TA were lower in PUT-treated fruit, while TA and ascorbic acid content showed the reverse trend. In conclusion, pre-storage 2.0 mM PUT treatment inhibited ethylene production and suppressed the activities of cell wall enzymes, while resulting in higher activities of antioxidative enzymes and maintaining better fruit quality during ripening and cold storage.     

Effect of hyperbaric,controlled atmosphere,and UV treatments on peach volatiles

The effect of hyperbaric (HP) and controlled atmosphere (CA) storage and prestorage treatment with ultra violet (UV) radiation on the volatile chemistry of peach [Prunus persica (L.) Batsch] fruit was assessed. Peach volatiles were analyzed using a dynamic headspace system with Tenax trap, automated short path thermal desorption, and GC–MS. The composition of volatile compounds emanating from the fruit varied quantitatively and qualitatively with storage (4 weeks). A total of 65 volatiles were identified, 21 prior to storage and 59 after 4 weeks storage. Six of the prestorage volatiles were not found after storage. The concentration of total volatiles and esters, the highest relative proportion of primary classes increased 32.5- and 36.5-fold, respectively, during storage. Ethyl butanoate, ethyl hexanoate, and ethyl heptanoate contributed to peach aroma due to their low odor thresholds and high concentrations. Using a factorial design (2 × 2 × 2), the main effects [storage pressure (P), storage gas atmosphere (A), and UV pretreatment] and interactions (P × A, P × UV, A × UV, and P × A × UV) were determined. P contributed most to the concentration of total volatile compounds followed by A; HP and HP + CA with or without UV significantly reduced the concentration of total volatiles and esters. Prestorage UV irradiation treatment did not affect the emission of volatile compounds. Principal component analysis (PCA) using 59 volatile compounds emanating from stored fruit indicated a significant effect of P and A on the emission of volatiles that were divided into four treatment groups accounting for 67.5% of the total variance, i.e., AP + Air, AP + CA, HP + Air, and HP + CA. The PCA distribution indicated which compounds contributed most to differences in volatile pattern among treatments: ethyl (Z)-4-octenoate, ethyl heptanoate, ethyl octanoate, and decanal (AP + Air); 3-methylbutyl acetate, ethyl butanoate, ethyl hexanoate, and 2-methylbutanoate (HP + CA); nonanal and hexanal (AP + CA); and hexyl acetate (HP + Air).     

Respiration and quality responses of sweet cherry to different atmospheres during cold storage and shipping

Most sweet cherries produced in the US Pacific Northwest and shipped to distant markets are often in storage and transit for over 3 weeks. The objectives of this research were to study the effects of sweet cherry storage O₂ and CO₂ concentrations on the respiratory physiology and the efficacy of modified atmosphere packaging (MAP) on extending shelf life. Oxygen depletion and CO₂ formation by ‘Bing’ and ‘Sweetheart’ cherry fruit were measured. While respiration rate was inhibited linearly by reduced O₂ concentration from 21% to 3–4% at 20 °C, it was affected very little from 21% to ∼10% but declined logarithmically from ∼10% to ∼1% at 0 °C. Estimated fermentation induction points determined by a specific increased respiratory quotient were less than 1% and 3–4% O₂ for both cultivars at 0 and 20 °C, respectively. ‘Bing’ and ‘Sweetheart’ cherry fruits were packaged (∼8 kg/box) in 5 different commercial MAP box liners and a standard macro-perforated polyethylene box liner (as control) and stored at 0 °C for 6 weeks. MAP liners that equilibrated with atmospheres of 1.8–8.0% O₂ + 7.3–10.3% CO₂ reduced fruit respiration rate, maintained higher titratable acidity (TA) and flavor compared to control fruit after 4 and 6 weeks of cold storage. In contrast, MAP liners that equilibrated with atmospheres of 9.9–14.4% O₂ + 5.7–12.9% CO₂ had little effect on inhibiting respiration rate and TA loss and maintaining flavor during cold storage. All five MAP liners maintained higher fruit firmness (FF) compared to control fruit after 6 weeks of cold storage. In conclusion, storage atmospheres of 1.8–14.4% O₂ + 5.7–12.9% CO₂ generated by commercial MAP, maintained higher FF, but only the MAP with lower O₂ permeability (i.e., equilibrated at 1.8–8.0% O₂) maintained flavor of sweet cherries compared to the standard macro-perforated liners at 0 °C. MAP with appropriate gas permeability (i.e., equilibrated at 5–8% O₂ at 0 °C) may be suitable for commercial application to maintain flavor without damaging the fruit through fermentation, even if temperature fluctuations, common in commercial storage and shipping, do occur.     

Relationship of IAD index to internal quality attributes of apples treated with 1-methylcyclopropene and stored in air or controlled atmospheres

The research was conducted to evaluate the relationship between I_AD index (index of absorption difference between 670 and 720 nm) values and internal quality attributes of apples treated with 1-methylcyclopropene (1-MCP) and stored in air and controlled atmospheres (CA). Apples of ‘8S6923’ (Aurora Golden Gala™), ‘Fuji’ and ‘Royal Gala’ were tested. The results with Aurora Golden Gala™ show that I_AD index values were maintained at higher levels if the fruit were stored in CA and that 1-MCP had no significant effect on retaining at-harvest values. The I_AD values correlated with chlorophyll a content in the peel (R² = 0.95, P < 0.0001), but not with chlorophyll b content, internal ethylene levels, firmness or titratable acidity. ‘Royal Gala’ apples showed a similar response to Aurora Golden Gala™ apples, showing no correlation between I_AD index values and internal quality attributes of those apples when treated with 1-MCP and/or CA. In contrast, ‘Fuji’ apples showed a relationship between I_AD index value changes and internal ethylene concentrations (R² = 0.67, P < 0.05) and titratable acidity changes (R² = 0.89, P < 0.01), but not firmness. These results suggest that when 1-MCP and/or CA are applied to apples after harvest, that I_AD index values do not consistently correlate to any internal quality attributes other than peel chlorophyll a content.     

Postharvest quality of peeled prickly pear fruit treated with acetic acid and chitosan

White (Opuntia albicarpa) and red (Opuntia ficus-indica) prickly pears were peeled and submerged in chitosan solutions containing different concentrations of acetic acid (1.0 or 2.5%) to obtain ready-to-eat prickly pear products. Some physicochemical (pH, total soluble solids, color, weight loss, and firmness), antioxidant (phenolic compounds and antioxidant activity), microbiological (aerobic mesophile bacteria and yeasts plus molds), and sensory (color, firmness, aroma, flavor, and overall acceptance) characteristics were assessed during 16 d of storage at 4 ± 1 °C and 85 ± 5% of relative humidity. Chitosan coating containing 1.0% of acetic acid delayed weight loss, maintained firmness and color of white prickly pear during the storage time. Most of the sensory values for white prickly pear coated with chitosan containing 1.0 and 2.5% of acetic acid were higher than those obtained for uncoated fruit. Red prickly pear coated with chitosan with 2.5% acetic acid did not maintain its sensory quality throughout 16 d of storage. Chitosan coating with 1 and 2.5% acetic acid did not affect phenolics content and antioxidant activity in white prickly pears; however, an increase of these compounds was observed in red prickly pears. Microbe populations were unchanged in white prickly pears (<10 CFU g⁻¹) and slightly increased in red prickly pears (10–500 CFU g⁻¹) coated with chitosan during the entire storage time.