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.     

Inhibition of browning on the surface of apple slices by short term exposure to nitric oxide (NO) gas

Freshly cut slices of apple (Malus x domestica Borkh cv. Granny Smith) were fumigated with nitric oxide (NO) gas at concentrations between 1 and 500 μl l⁻¹ in air at 20 °C for up to 6 h followed by storage at 0, 5, 10 and 20 °C in air. Exposure to nitric oxide delayed the onset of browning on the apple surface with the most effective treatment being fumigation with 10 μl l⁻¹ NO for 1 h. While nitric oxide inhibited browning in slices held at all temperatures, it was relatively more effective as the storage temperature was reduced with the extension in postharvest life over the respective untreated slices increasing from about 40% at 20 °C to about 70% at 0 °C. In a smaller study on ‘Royal Gala’, ‘Golden Delicious’, ‘Sundowner’, ‘Fuji’ and ‘Red Delicious’ slices stored at 10 °C, 10 μl l⁻¹ NO for 1 h was found to be effective in inhibiting surface browning in all cultivars.     

Phomopsis longanae Chi-induced pericarp browning and disease development of harvested longan fruit in association with energy status

The effects of Phomopsis longanae Chi infection on browning development and disease incidence in relation to energy status in pericarp of harvested longan fruit were investigated. Longan fruit were inoculated for 5 min with P. longanae at 10⁴ spores mL⁻¹, while fruit dipped in sterile deionized water were used as control. These fruits were stored at (28 ± 1) °C and 90% relative humidity for up to five days. The results showed that the browning index, disease incidence, cellular membrane permeability and AMP content increased but the contents of ATP and ADP, and energy charge decreased in pericarp of longan fruit infected by P. longanae. It was suggested that P. longanae infection caused energy deficiency in longan fruit, possibly resulting in accelerated senescence and decreased resistance to pathogen, and thus promoted browning development and disease occurrence.     

1-Methylcyclopropene (1-MCP) delays senescence,maintains quality and reduces browning of non-climacteric eggplant (Solanum melongena L.) fruit

Ethylene action can be counteracted by 1-methylcyclopropene (1-MCP), which has been used during postharvest storage to maintain quality. In this work, we evaluated the effect of 1-MCP treatments on eggplant quality and phenolic metabolism during refrigerated storage. Eggplants (cv. Lucía) were harvested at commercial maturity, treated with 1-MCP (1 μL/L, 12 h at 20 °C), stored at 10 °C for 21 d and subsequently held at 20 °C for 2 d. Corresponding controls were stored at 10 °C and then transferred to 20 °C for 2 d. During storage calyx color, damage and chlorophyll content, fruit weight loss and firmness, pulp sugar content, acidity, browning and total phenolics were measured. In addition, polyphenol oxidase (PPO), pyrogallol peroxidase (POD), and phenylalanine ammonia-lyase (PAL) activities were evaluated. Fruit calyxes showed reduced damage and remained greener in 1-MCP treated than in control fruit. 1-MCP treated eggplants showed lower weight loss. Pulp browning was clearly prevented as a consequence of 1-MCP exposure, and this was associated with delayed senescence, lower accumulation of total phenolics and reduced activity of PAL. The activity of the enzymes PPO and POD involved in the oxidation of phenolics compounds was also decreased in 1-MCP treated fruit. Results suggest that 1-MCP treatments delay senescence, prevent browning and are beneficial to complement low temperature storage and maintain quality of non-climacteric eggplant fruit.     

Effects of preharvest nitric oxide treatment on ethylene biosynthesis and soluble sugars metabolism in ‘Golden Delicious’ apples

In order to examine the influence of preharvest nitric oxide (NO) treatment on ethylene biosynthesis and soluble sugar metabolism in ‘Golden Delicious’ apples, apple trees were sprayed with 50 μM sodium nitroprusside (SNP) (a donor of NO) 14 days before harvest. The results indicated that preharvest SNP treatment can increase the NO content and the NOS activity in apple fruit, therefore, delay the accumulation of ethylene due to its inhibition on the activities of 1-aminocyclopropane-1-carboxylate synthase (ACS) and 1-aminocyclopropane-1-carboxylate oxydase (ACO). Fructose is the main sugar in ‘Golden Delicious’ apple. The synthesis of sucrose was stimulated and the decomposition of sucrose was inhibited by this treatment, thus causing the accumulation of sucrose. We can draw a conclusion that pre-harvest SNP (50 μM) treatment can increase the NO content of fruit during storage, while higher NO content can further regulate fruit ripening through its effect on ethylene and sugar metabolism in ‘Golden Delicious’ apple fruit during storage at 18 °C.     

Preharvest application of abscisic acid promotes anthocyanins accumulation in pericarp of litchi fruit without adversely affecting postharvest quality

Pericarp colour of litchi fruit is an important quality attribute that determines its market value and consumer acceptance. Plant growth regulators (PGR) such as abscisic acid (ABA) and ethephon are known to play important roles in peel colour development during maturation and ripening of non-climacteric fruits (e.g. grape and litchi). Our aim was to investigate the effects of preharvest application of ABA, ethephon and their combination on pericarp colour and fruit quality of litchi (cv. Calcuttia) and also to assess the potential effects on postharvest performance of fruit. Exogenous application of ABA (150 or 300 mg L⁻¹) at the colour-break stage significantly increased the concentration of total anthocyanins and cyanidin-3-O-rutinoside, the major anthocyanin contributing ∼71–96% of the total anthocyanins, in litchi pericarp compared to ethephon (500 μL L⁻¹). Among different anthocyanins quantified, the relative contribution of cyanidin-3,5-diglucoside to the total anthocyanins was significantly higher in all PGR-treated fruit compared to the control, but the concentration of cyanidin-3-O-glucoside was specifically enhanced by ABA. No significant effect on the concentrations of epicatechin, and quercetin-3-O-rutinoside was observed in response to PGR treatments. Ethephon (500 μL L⁻¹) treatment did not significantly increase the anthocyanin levels in pericarp, but it caused more degradation of chlorophyll pigments than control. Aril quality with regard to firmness, soluble solids and acidity was not significantly affected by PGR treatments, except that ethephon-treated fruit showed significant softening and lower acidity. Postharvest changes in fruit quality attributes including pericarp browning during cold storage at 5 °C for 14 d were mainly related to the storage duration effect, rather than PGR treatment. In conclusion, ABA treatment (150 or 300 mg L⁻¹) at the colour-break stage enhanced anthocyanins accumulation in litchi pericarp without adversely affecting postharvest quality and storage stability for 14 d.     

Use of hot water treatment to control codling moths in harvested California ‘Bing’ sweet cherries

Preharvest gibberellic acid-treated California ‘Bing’ sweet cherries (Prunus avium L.) were treated with hot water baths (46–58 °C for 0.25–18 min), followed by hydrocooling. The fruit were then stored to simulate either air shipment or sea shipment to overseas markets, both followed by 15 h of shelf life at 20 °C. In separate experiments, cherries were also infested with codling moth larvae and subjected to similar hot water bath heating. The quality attributes showed different sensitivity to the combinations of temperature and time used for hot water bath treatment. Pitting was more common in fruit treated at lower temperatures for longer times, while stem browning was more common in fruit treated at high temperatures. Berry browning, stem color, and pitting were the quality attributes most affected by heat treatment. Browning of cherry stem color was a crucial factor in determining whether a combination of temperature and time for hot water bath treatment was successful. All cherries stored at 0 °C for 14 days to simulate sea shipment were of unacceptable quality after shelf life. Hot water bath treatments that provided 100% codling moth mortality and maintained overall acceptable fruit quality were very limited and included treatments at 50 °C for 10 min and at 54 °C for 6 min. Delaying the hot water bath treatment after fruit harvest, even if the cherries were kept at 0 °C, resulted in a greater loss in fruit quality compared with those treated on the harvest day. Using hot water baths as a quarantine treatment for codling moths (Cydia pomonella) on sweet cherries may be feasible if fruit are air shipped at 5 °C for 2 days, but not suitable if fruit are sea shipped at 0 °C for 14 days.     

Amelioration of chilling stress by arginine in tomato fruit: Changes in endogenous arginine catabolism

Freshly harvested tomato fruit were pretreated with 0.2 mM arginine at −35 kPa for 0.5 min and then stored at 2 °C for 28 d to investigate the effect of exogenous arginine treatment on endogenous arginine catabolism in relation to chilling injury (CI). Arginine treatment reduced the CI index of fruit and enhanced accumulation of polyamines, especially putrescine, and proline, which resulted from the increased activities of the catabolic enzymes arginase, arginine decarboxylase, ornithine decarboxylase and ornithine δ-aminotransferase at most sampling times. Nitric oxide synthase activity was also increased by arginine treatment, which at least partly contributed to the increased nitric oxide concentration. These results revealed that the reduction in CI by exogenous arginine may be due to the accumulation of putrescine, proline and nitric oxide induced by activating the different pathways of endogenous arginine catabolism.     

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.     

Effect of nitric oxide (NO) and associated control treatments on the metabolism of fresh-cut apple slices in relation to development of surface browning

Surface browning is an important cause of deterioration of fresh-cut apples during postharvest handling. ‘Granny Smith’ apple slices treated with NO gas (10 μL/L) and the NO donor compound 2,2′-(hydroxynitrosohydrazino)-bisethanamine (diethylenetriamine nitric oxide (DETANO) (10 mg/L) dissolved in phosphate buffer (pH 6.5) showed delayed development of surface browning during storage at 5 °C and also resulted in a lower level of total phenols, inhibition of PPO activity, reduced ion leakage and reduced rate of respiration but had no significant effect on ethylene production or lipid peroxide level as measured by malondialdehyde (MDA) and hydrogen peroxide levels. The two control treatments of phosphate buffer (pH 6.5) and water dips also had significant effects compared to untreated slices. The relative effectiveness of treatments in extending postharvest life and reducing total phenols, PPO activity, ion leakage and respiration was DETANO > NO gas > phosphate buffer > water > untreated. Apple slices dipped in chlorogenic acid dissolved in water showed surface browning soon after application but dipping in DETANO solution negated the effect of chlorogenic acid whether applied before or after dipping in chlorogenic acid solution while the buffer and NO gas were also effective. It is suggested that an increase in phenols occurs on the apple surface soon after cutting, possibly as a defensive mechanism of the apple to limit damage to surface cells. The effectiveness of the applied treatments to inhibit development of surface browning may relate to their ability to minimize the level of phenols active on the cut surface possibly in conjunction with a reduced PPO activity.     

Improved quality retention of packaged ‘Anjou’ pear slices using a 1-methylcyclopropene (1-MCP) co-release technology

After three months storage at 0.5 °C one quarter of a lot of ‘Anjou’ pears (Pyrus communis L.) were treated with 1 μL L^?1 of 1-methylcyclopropane (1-MCP) for 8 h at 20 °C and three quarters of the fruit were left untreated at 20 °C for the same time. Treated and untreated pears were then sliced, dipped in a commercial anti-browning solution and packaged in modified atmospheric bags. Packages, containing slices from 1-MCP treated fruit, were labelled as MCP1. Slices from two thirds of the untreated fruit had one of two secondary treatments applied: (1) multi-functional co-release sachets added to the package at the time of sealing (NT), or (2) an injection of 1-MCP to sealed packages to achieve a final concentration of 1 μL L^?1 (MCP2). The last third of the slices from the untreated lot of pears were sealed into packages with no further treatment (CK). The packages were kept at 5 °C. In-package ethylene concentrations were significantly lower for the NT treated slices. NT also significantly delayed and reduced net oxygen consumption in the package headspace compared with other treatments. The NT treatment also reduced incidence of browning induced by enzymes of microbial origin, termed secondary browning (SB), and better maintained the measured juiciness of slices. In contrast, the CK, MCP1 and MCP2 treatments showed a more rapid appearance and severity of SB. Slices in packages treated with NT retained higher tissue levels of butyl, hexyl and pentyl acetate, 6-methyl-5-hepten-2-one, butanol and hexanol during storage than any of the other three treatments.     

Hexanal reduces infection of tomatoes by Botrytis cinerea whilst maintaining quality

Hexanal vapour and intact tomatoes were used as models to assess the opportunities for control of Botrytis cinerea rots by controlled release of organic vapours. Hexanal vapour concentrations in the ranges 5–270 μL L⁻¹ were applied continuously or as a single dose at the start of storage. The postharvest microbiological, physiological and quality attributes of control and hexanal treated tomatoes were investigated during storage for 7 days at 20 ± 1 °C and ∼99% RH. Continuous hexanal exposure effectively suppressed grey mould with the minimum inhibitory concentration (MIC) being 40–70 μL L⁻¹; the single-dose treatment showed minimal antifungal activity. During continuous exposure at the MIC the fruit respiration rate was increased ∼50% and reddening was slowed. No clear trend was observed in ethylene production and treated fruit did not differ from the controls in firmness or mass loss. The controlled release of low concentrations of hexanal vapour into a packaging headspace appears a feasible mechanism for prolonging tomato storage life.     

Postharvest nitric oxide fumigation delays fruit ripening and alleviates chilling injury during cold storage of Japanese plums (Prunus salicina Lindell)

We investigated the effects of nitric oxide (NO) fumigation on fruit ripening, chilling injury, and quality of Japanese plums cv. ‘Amber Jewel’. Commercially mature fruit were fumigated with 0, 5, 10, and 20 μL L⁻¹ NO gas at 20 °C for 2 h. Post-fumigation, fruit were either allowed to ripen at 21 ± 1 °C or were stored at 0 °C for 5, 6, and 7 weeks followed by ripening for 5 d at 21 ± 1 °C. NO-fumigation, irrespective of concentration applied, significantly (P ≤ 0.5) suppressed respiration and ethylene production rates during ripening at 21 ± 1 °C. At 21 ± 1 °C, the delay in ripening caused by NO-fumigation was evident from the restricted skin colour changes and retarded softening in fumigated fruit. NO treatments (10 and 20 μL L⁻¹) delayed the decrease in titratable acidity (TA) without a significant (P ≤ 0.5) effect on soluble solids concentration (SSC) during ripening. During 5, 6, and 7 weeks of storage at 0 °C, NO-fumigation was effective towards restricting changes in the ripening related parameters, skin colour, firmness, and TA. The individual sugar (fructose, glucose, sucrose, and sorbitol) profiles of NO-fumigated fruit were significantly different from those of non-fumigated fruit after cold storage and ripening at 21 ± 1 °C. CI symptoms, manifest in the form of flesh browning and translucency, were significantly lower in NO-fumigated fruit than in non-fumigated fruit after 5, 6, and 7 weeks storage followed by ripening for 5 d at 21 ± 1 °C. NO-fumigation was effective in reducing decay incidence in plums during ripening without storage and after cold storage at 0 °C for 5, 6, and 7 weeks. In conclusion, the postharvest exposure of ‘Amber Jewel’ plums to NO gas (10 μL L⁻¹) delayed ripening by 3–4 d at 21 ± 1 °C, and also alleviated chilling injury symptoms during cold storage at 0 °C for 6 weeks.     

Efficacy of ethanolic extract of propolis in maintaining postharvest quality of dragon fruit during storage

Significant (P ≤ 0.05) differences were observed in dragon fruit quality when treated with different concentrations of ethanolic extract of propolis (EEP) (0.25, 0.50, 0.75 and 1.0%) and stored at 20 ± 2 °C and 80 ± 5% relative humidity (RH) for 20 days. Fruit treated with 0.50% EEP showed the most promising results, while fruit treated with 0.75 and 1.0% EEP showed some phytotoxic effects even after 8 days of storage. The results of gas exchange analysis also proved the efficacy of 0.50% EEP concentration. Thus, it can be concluded from the present investigation that EEP at 0.50% concentration could be used to extend the storage life of dragon fruit without any negative effects on the quality.     

Influence of film wrapping and fludioxonil application on quality of pomegranate fruit

Pomegranates are sensitive to low temperatures. When fruit are exposed to temperatures below 5–6 °C chilling injury appears as pitting of the skin, browning of the white segments separating the arils and discoloration of the arils, and husk scald, which generally is more severe at temperatures of 6–10 °C. The main objective of this work was to assess the effectiveness of individual film packaging, applied as a stand alone treatment or in combination with fludioxonil, on reducing the occurrence of husk scald, weight loss and decay. Fruit were dipped in an aqueous mixture containing 600 mg L^?1 fludioxonil, wrapped or not wrapped with a polyolephinic heat-shrinkable film and stored at 8 °C and 90% RH for 6 or 12 weeks plus one additional week of simulated shelf-life at 20 °C and 65–70% RH. Respiration rate decreased both in cold storage and at 20 °C. Ethylene production was not detected during cold storage; its rate increased upon transfer to 20 °C, but results were inconsistent. Control fruit deteriorated at a very high rate, due to excessive weight loss, skin browning and decay. Film wrapping almost completely inhibited weight loss and husk scald and preserved fruit freshness for the whole storage time. There was no statistical difference in decay incidence between wrapped and control fruit after 6 or 12 weeks of storage and after the first shelf-life, while after the second shelf-life, wrapped fruit had significantly higher decay levels. By contrast, fludioxonil, both alone and in combination with wrapping, effectively controlled mold development, resulting in 50–67% less decay than control fruit after 12 weeks at 8 °C plus one week shelf-life. Control fruit showed minor changes in nutritional compounds as well as in total polyphenols, anthocyanins and antioxidant activity, while higher losses were detected in film-wrapped fruit during storage at 20 °C.     

Magnetic resonance imaging provides spatial resolution of Chilling Injury in Micro-Tom tomato (Solanum lycopersicum L.) fruit

Magnetic resonance imaging (MRI) was used to monitor internal changes in harvested tomato (Solanum lycopersicum L. cv. Micro-Tom) fruit. Measurements of ethylene evolution, respiration, and ion leakage indicated that the fruit developed chilling injury (CI) after storage at 0 °C. Unlike these measurements, MRI provided spatially resolved data. The apparent diffusion coefficient (ADC), which is an indication of water mobility in tissues, was calculated from MRIs of the different parts of the fruit. Storage for 1 or 2 weeks at 0 °C caused no difference in the ADCs (D-values) in the pericarp, but it did lead to higher values in the inner tissues i.e., the columella and locular region compared to non-chilled fruit (P < 0.05). Changes in inner fruit D-values after 1 and 2 weeks of chilling at 0 °C were similar to changes in respiration, ethylene production and ion leakage which increased (P < 0.05) compared to the non-chilled controls. Most CI studies of tomato fruit used pericarp tissue. Our data indicate that columella tissue changes occur in response to chilling injury in tomato fruit and suggest that more caution is needed when interpreting data from experiments commonly used to study this phenomenon.     

Postharvest litchi (Litchi chinensis Sonn.) quality preservation by Lactobacillus plantarum

The objective of this work was to preserve the postharvest quality of litchi cv Brewster by the application of Lactobacillus plantarum. A suspension of 1 × 10⁹ CFU/mL of the bacteria was sprayed on ripe litchis and then stored at 10 °C with 75% of relative humidity. Treated fruit exhibited a significantly higher Gram positive bacteria growth on the rind (4–5 log CFU/g) than that detected in control fruit (2.5–3.75 log CFU/g). This result was corroborated by observing a high population of lactobacilli in scanning electron micrographs and by measurement of the content of lactic acid produced. Treated fruit displayed significantly (α ≤ 0.05) reduced color losses as indicated by the higher L* and C* values in comparison with the untreated ones. Additionally, cyanidin-3-rutinoside and total anthocyanin contents supported the measured color retention, since the pericarp of fruit treated with Lb. plantarum showed a significantly higher concentration of pigments than those used as control. In addition, a high concentration of phenolic compounds was found in the rind of treated fruit.     

Preharvest application of methyl jasmonate (MeJA) in two plum cultivars. 2. Improvement of fruit quality and antioxidant systems during postharvest storage

‘Black Splendor’ (BS) and ‘Royal Rosa’ (RR) plums were treated preharvest with methyl jasmonate (MeJA) at three concentrations (0.5, 1.0 and 2.0 mM) along the on-tree fruit development: 63, 77 and 98 days after full blossom (DAFB). Both control and treated fruit were harvested at the commercial ripening stage and stored in two temperature conditions: 9 days at 20 °C or at 2 °C + 1 day at 20 °C for 50 days. Preharvest MeJA at 2.0 mM significantly accelerated whereas 0.5 mM delayed the postharvest ripening process for both cultivars, since ethylene production, respiration rate and softening were reduced significantly at the two storage conditions for 0.5 mM. In these fruit, total phenolics, total antioxidant activity (hydrophilic fraction, HTAA) and the antioxidant enzymes peroxidase (POD), catalase (CAT) and ascorbate peroxidase (APX) were found at higher levels in treated than control plums during postharvest storage, which could account for the delay of the postharvest ripening process and the extension of shelf-life.     

Effect of antioxidants in controlling enzymatic browning of minimally processed persimmon ‘Rojo Brillante’

‘Rojo Brillante’ is an important variety of persimmon that after removal of the astringency with high levels of CO₂, maintains firmness and sweetness, making possible its commercialization as a fresh-cut commodity. However, the commercial success of the product is limited mainly by enzymatic browning. This work presents the effect of a wide range of antioxidants on enzymatic browning of ‘Rojo Brillante’ persimmon combining in vitro (extracts and precipitates) and in vivo (cut tissue) studies. Preliminary screening of the antioxidants, determined by absorbance and color measurements of persimmon extracts and pellets, showed that 4-hexylresorcinol (Hexyl), citric acid (CA) and calcium chloride (CaCl₂) were effective at controlling browning at 10 mM; whereas, ascorbic acid (AA) required a higher concentration (25 mM). Peracetic acid, cyclodextrin, cysteine, and hexametaphosphate were not effective at controlling browning, even at a concentration of 50 mM. In in vivo studies, AA (1.12%) and CA (0.21%) were the most effective treatments to control enzymatic browning of fresh-cut material, reaching the limit of marketability in 5–7 days, whereas, Hexyl and CaCl₂ did not reach 1 day of storage. The results showed that optimum concentrations in cut tissue did not always correlate with the in vitro studies, indicating that antioxidants have an effect not only in browning reactions, but also in metabolic activity and cell wall changes during wound-induced reactions. The results provide relevant information for further development of minimally processed ‘Rojo Brillante’ persimmon during storage at 5 °C.     

Preharvest application of methyl jasmonate (MeJA) in two plum cultivars. 1. Improvement of fruit growth and quality attributes at harvest

Two plum (Prunus salicina Lindl.) cultivars ‘Black Splendor’ (BS) and ‘Royal Rosa’ (RR) were treated with methyl jasmonate (MeJA) at 3 concentrations (0.5, 1.0 and 2.0 mM) along the on-tree fruit development: 63, 77 and 98 days after full blossom (DAFB). On a weekly basis, fruit samples were taken for measuring fruit size and weight and parameters related to quality. Results revealed that MeJA was effective in increasing fruit size and weight, the 0.5 mM being the most effective for BS cultivar and 2.0 mM for RR. At harvest, those fruit treated with 0.5 mM MeJA had the highest firmness and colour Hue values. Total acidity was also generally higher in MeJA-treated fruit than in controls, while the content of total soluble solids remained unaffected. In addition, total phenolics and total antioxidant activity were found at higher concentrations in 0.5 and 2.0 mM MeJA-treated than in control fruit over at last 3 weeks of fruit development for BS and RR cultivars, respectively. Overall results suggest that MeJA could be a promising preharvest tool to increase plum size and quality with enhanced bioactive compounds and antioxidant activity, although the optimum concentration is cultivar dependent.