Application of low concentrations of ozone during the cold storage of table grapes

The control by ozone of postharvest decay of table grapes, caused by Botrytis cinerea and other pathogens, was evaluated in chambers and commercial storage facilities. Ozone at 0.100 μL/L or higher inhibited the spread of gray mold among stored grapes. Ozone diffusion into many types of commercial packaging was measured. Boxes made of uncoated paper corrugate inhibited diffusion more than those composed of coated paper corrugate, plastic corrugate, hard plastic, or expanded polystyrene. Internal packaging of hard plastic clamshell containers inhibited diffusion less than low density polyethylene cluster bags. Atmospheres of 0.100 μL/L ozone in the day and 0.300 μL/L at night reduced the natural incidence of gray mold by approximately 65% after 5–8 weeks of storage. Its effectiveness to control postharvest decay was compared to sulfur dioxide fumigation. After 68 days at 1 °C the incidence of gray mold among grapes stored in air, ozone, or with weekly sulfur dioxide fumigation was 38.8%, 2.1%, and 0.1%, respectively. However, decay by other fungi, such as Alternaria spp. and Penicillium spp., was controlled by sulfur dioxide, but not by ozone. In some tests, rachis appearance was moderately harmed by ozone. The combination of ozone use in storage following a single initial sulfur dioxide fumigation, or its use in between biweekly sulfur dioxide fumigations, controlled both gray mold and other pathogens and matched the commercial practice of initial and weekly sulfur dioxide fumigation. The use of both gases in this way reduced sulfur dioxide use greatly. Differences in flavor of grapes treated with ozone were not detectable compared to those stored in air, and grapes treated with ozone were preferred over those treated with sulfur dioxide.     

Influence of fumigation with high concentrations of ozone gas on postharvest gray mold and fungicide residues on table grapes

To control postharvest decay, table grapes are commercially fumigated with sulfur dioxide. We evaluated ozone (O₃) fumigation with up to 10,000 μL L^?1 of ozone for up to 2 h to control postharvest gray mold of table grapes caused by Botrytis cinerea. Fumigation for 1 h with 2500 or 5000 μL L^?1 of ozone were equal in effectiveness. Both treatments reduced postharvest gray mold among inoculated ‘Thompson Seedless’ grapes by approximately 50% when the grapes were examined after storage for 7 d at 15 °C following fumigation. In a similar experiment, ‘Redglobe’ grapes were stored for 28 d at 0.5 °C following fumigation for 1 h with 2500 or 5000 μL L^?1 of ozone. Both treatments were equal in effectiveness, but inferior to fumigation with 10,000 μL L^?1. Ozone was effective when grapes were inoculated and incubated at 15 °C up to 24 h before fumigation. The cluster rachis sustained minor injuries in some tests, but berries were never harmed. Ozone was applied in three combinations of time and ozone concentration (10,000 μL L^?1 for 30 min, 5000 μL L^?1 for 1 h, and 2500 μL L^?1 for 2 h) where each had a constant concentration × time product (c × t) of 5000 μL L^?1 × h. The effectiveness of each combination was similar. The incidence of gray mold was reduced by approximately 50% among naturally inoculated, organically grown ‘Autumn Seedless’ and ‘Black Seedless’ table grapes, and by 65% among ‘Redglobe’ table grapes, when they were fumigated with 5000 μL L^?1 ozone for 60 min in a commercial ozone chamber and stored for 6 weeks at 0.5 °C. Residues of fenhexamid, cyprodinil, pyrimethanil, and pyraclostrobin were reduced by 68.5, 75.4, 83.7, and 100.0%, respectively, after a single fumigation of table grapes with 10,000 μL L^?1 ozone for 1 h. Residues of iprodione and boscalid were not significantly reduced. Ozone is unlikely to replace sulfur dioxide treatments in conventional grape production unless its efficacy is improved, but it could be an acceptable technology to use with grapes marketed under “organic” classification, where the use of SO₂ is prohibited, or if SO₂ use were to be discontinued.     

Control of fungal decay of apples and peaches by the biofumigant fungus Muscodor albus

The potential of the volatile-producing fungus Muscodor albus for controlling postharvest diseases of fresh fruit by biological fumigation was investigated. In vitro tests showed that M. albus volatiles inhibited and killed a wide range of storage pathogens belonging to species of Botrytis, Colletotrichum, Geotrichum, Monilinia, Penicillium and Rhizopus. Fumigation of apples for 7 days with culture of M. albus grown on autoclaved grain gave complete control of blue mold (Penicillium expansum) and gray mold (Botrytis cinerea) in wound-inoculated fruits. There was no direct contact between the fruit and the M. albus culture. Shorter fumigation times ranging between 24 and 72 h, applied immediately or 24 h after inoculation, also controlled blue mold and gray mold. In wound-inoculated peaches, 24–72 h fumigation with M. albus provided complete control of brown rot (Monilinia fructicola). The volatile profile of M. albus-colonized grain was measured by gas chromatograph connected to a flame ionization detector (GC-FID) and showed that 2-methyl-1-butanol and isobutyric acid were the major volatile compounds found in the headspace. Since M. albus is a sterile mycelium and does not require direct contact with the crops to be treated, it could be an attractive biological fumigant for controlling postharvest diseases.     

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.     

Preharvest applications of growth regulators and their effect on postharvest quality of table grapes during cold storage

Over 54,600 ha of table grapes (Vitis vinifera), mainly cvs. ‘Thompson Seedless’, ‘Flame Seedless’ and ‘Redglobe’, are planted in Chile. Almost the entire production is exported to the USA, Europe, Asia, or one of several Latin American countries, which typically requires 15–40 d of maritime transportation. During this period, several physical, physiological, and pathological factors cause table grape deterioration. Because berry size is the main quality factor in international markets, farmers often overuse the growth regulators, gibberellic acid (GA₃) and forchlorfenuron (CPPU), in an effort to increase berry size. We examined the effect of preharvest growth regulators on seedless (‘Thompson Seedless’, and ‘Ruby Seedless’) and seeded (‘Redglobe’) table grape cultivars during cold (0 °C) storage plus a shelf life period of 3 d at 20 °C. The overuse of GA₃, eight instead of two GA₃ applications on Thompson Seedless, and the use of one GA₃ application on Redglobe and ‘Ruby Seedless’, increased berry pedicel thickness and lowered cuticle content but induced shatter and predisposed grapes to gray mold caused by Botrytis cinerea. In contrast, CPPU increased berry pedicel thickness and cuticle content but did not increase shatter or gray mold incidence. Clusters that were subjected to overuse of combined GA₃ and CPPU were highly sensitive to shatter, had the thickest pedicel, and developed a high gray mold incidence during cold storage. Hairline, a fine cracking developed during cold storage, was induced on ‘Thompson Seedless’ and ‘Ruby Seedless’ by growth regulators, but no hairline occurred on ‘Redglobe’ table grapes. Therefore, berry quality during cold storage is greatly influenced by growth regulator management in the vineyard.     

Determination of optimal sulfur dioxide time and concentration product for postharvest control of gray mold of blueberry fruit

Highbush blueberries (Vaccinum spp.) are a major export fruit crop of Chile which is stored at 0 °C and transported to markets in Asia, Europe, and the USA, using more than 15 d of maritime transportation. Under these conditions, gray mold caused by Botrytis cinerea can produce important economic losses. The effectiveness of sulfur dioxide (SO₂) concentration × time treatments on gray mold control was determined in the laboratory and validated prior to refrigerating the fruit, using pallet scale SO₂ fumigation treatment on the following blueberry cultivars: ‘Brigitta’, ‘Legacy’, ‘Liberty’ and ‘O’Neal’. In inoculated ‘Brigitta’ and ‘Liberty’ blueberries, gray mold prevalence varied from 97.2% to 97.5% in non-treated fruit, and this value was reduced from 7.9% to 6.1% in blueberries that were exposed to a SO₂ concentration × time (Ct) product of 400 (μL L⁻¹) h. The relationship between SO₂ Ct products and gray mold prevalence under laboratory conditions was best explained by exponential models, which had a determination coefficient (R²) that ranged from 0.88 to 0.96. The estimated EC₉₀ values varied between 245 and 400 (μL L⁻¹) h, and the SO₂ Ct between 250 and 350 (μL L⁻¹) h was validated using a pallet scale application treatment to obtain the best control and minimal variation. No visual phytotoxicity symptoms of SO₂ were observed with the Ct that was tested in this study. Therefore, SO₂ fumigation was demonstrated to be an effective and practical technology for reducing the risk of blueberry gray mold decay during storage, and further effort should be given to register the use of this product for blueberries in the main Chilean export markets.     

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.     

Salt strategies to control Botrytis mold of ‘Benitaka’ table grapes and to maintain fruit quality during storage

Gray mold is the most common postharvest disease of table grapes in most regions of the world. The effect of eight salts, namely sodium silicate (SSi), sodium sulphate (SS), sodium carbonate (SC), sodium bicarbonate (SB), iron chelate (Fech), iron sulphate (FeS), ammonium bicarbonate (AB), and ammonium oxalate (AO) was determined in vitro on mycelial growth and spore suspension of Botrytis cinerea. In particular, SSi, SC, SB, FeS, and AB completely inhibited pathogen growth at 0.25% concentration. Six salt solutions at 1%, immersion or spray, were tested to verify their effect on grapes artificially inoculated with B. cinerea. All salts significantly reduced the percentage of gray mold as compared to control except for Fech after one week at 22 ± 1 °C. Three salt solutions were applied, in vivo, according to different strategies: (i) spraying before harvest, (ii) immersion after harvest, and (iii) the combination of pre- and postharvest treatments. Water was involved as a negative control while Rovral (a.i. iprodione) and SO₂ served for comparisons. After one month of cold storage at 2 ± 1 °C followed by one week of shelf-life at 22 ± 2 °C, the natural incidence of postharvest mold was mostly caused by B. cinerea. The efficacy of preharvest applications was noticeably high and statistically was not enhanced by further treatments after harvest. Salts applied only after harvest were not effective in suppressing Botrytis mold, with the exception of FeS. The influence of salts on physicochemical properties for berry quality was also monitored. The field application of salts can be considered as an appropriate regime to enhance their activity since no negative impact of their application on quality profile was observed. The incidence of gray mold can be significantly reduced using some salts which are safe for consumers and the environment.     

Postharvest treatment of polyamines maintains quality and extends shelf-life of table grapes (Vitis vinifera L.) cv. Flame Seedless

Investigations were carried out to verify the potential of putrescine and spermidine as a postharvest dip treatment for maintaining quality and extending storage life of table grapes (Vitis vinifera L.) cv. Flame Seedless during the 2012 and 2013 seasons. Grape clusters were manually harvested at the commercial mature stage and were dipped in different concentrations (0.0, 0.5, 1.0 and 1.5 mM) of putrescine and spermidine, and then stored at 3–4 °C, and 90–95% RH. Evaluation of physico-chemical parameters and other fruit quality attributes were made at 0 day (before treatment) and at 30, 45, 60 and 75 days of storage. Putrescine and spermidine at the lowest dose (0.5 mM) effectively maintained berry firmness, peel colour (L*, C*, h°) and stabilized anthocyanins as well as suppressing the activity of pectin methylesterase and reducing the rate of electrolyte leakage. The polyamines also retarded the degradation of TSS and TA while maintaining higher total phenol content and reduced decay incidence. Putrescine and spermidine at 1.0 mM exhibited almost similar effects with a 0.5 mM dose. The highest doses (1.5 mM) of both polyamines showed detrimental effects, especially on weight loss, decay incidence, rachis browning and organoleptic properties, as found in the control group, which was commercially acceptable only up to 45 days. Furthermore, analysis of linear regressions and correlations showed that many quality parameters were interdependent. The postharvest dip treatment of spermidine or putrescine at a dose of 0.5 mM for 5 min could be an effective means for prolonging storage and increasing shelf-life of ‘Flame Seedless’ grapes.     

Application of abscisic acid (ABA) at veraison advanced red color development and maintained postharvest quality of ‘Crimson Seedless’ grapes

‘Crimson Seedless’ is a popular table grape cultivar, but in warm-climates, its fruits often fail to develop adequate red color, even after they have been treated with ethephon. Application of abscisic acid (ABA) may improve color more effectively than ethephon, but its potential effects on postharvest quality must be considered before recommending its use on table grapes. Therefore, we compared the postharvest quality attributes of grapes treated preharvest with 250 μL L⁻¹ ethephon, the current industry standard, to that of grapes treated with 150 or 300 μL L⁻¹ ABA, or nontreated. Treatment with either ethephon or 150 μL L⁻¹ ABA allowed grapes to be harvested 10 d before nontreated fruit, and fruits treated with 300 μL L⁻¹ ABA attained marketable quality 30 d before nontreated fruit. Early harvest was possible because the treatments induced more rapid coloring of the grapes, and though total yield was not affected by any plant growth regulator (PGR), all PGRs doubled packable yields by improving the color of the grapes. ABA-treated grapes were characterized by superior appearance both in berries and clusters’ rachises compared to ethephon-treated and control grapes. Other quality attributes such as firmness, berry weight, decay incidence, and shatter remained unaffected among treatments. Therefore, ABA is an effective alternative to ethephon for enhancing the color and maintaining postharvest quality of ‘Crimson Seedless’ grapes.     

Evaluation of the use of chlorine dioxide by fogging for decreasing postharvest decay of fig

Postharvest diseases limit the storage period and marketing life of figs. The efficacy of chlorine dioxide by fogging was tested for the control of postharvest diseases of black fig (Ficus carica L. cv. Bursa Siyahi). Fruit were fogged with various concentrations of chlorine dioxide in a cold storage unit for 60 min at room temperature. Treated fruit were stored either in air or modified atmosphere bags for 7 d at 1 °C followed by 2 d shelf-life at 20 °C. Fogging at 300–1000 μL L⁻¹ significantly reduced natural incidence of decay, most of which was gray mold. The efficacies of fogging at 500 and 1000 μL L⁻¹ were at the same level and fogging at 1000 μL L⁻¹ was superior to that at 300 μL L⁻¹ in fruit stored in air. Modified atmosphere packaging did not improve the efficacy of fogging in reducing decay incidence. The epiphytic population on the fruit surface was similarly reduced by chlorine dioxide fogging. All treatments significantly reduced total microorganisms, fungal and bacterial populations in fruit. In addition, microorganisms in the storage atmosphere were significantly reduced. None of the treatments affected the visual quality and taste of fruit.     

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.     

Effectiveness of postharvest treatment with chitosan and other resistance inducers in the control of storage decay of strawberry

This study compared the effectiveness of practical grade chitosan when used in solution with acetic, glutamic, formic and hydrochloric acids, and a water-soluble commercial chitosan formulation, in controlling postharvest diseases of strawberry. The commercial chitosan formulation and other resistance inducers based on benzothiadiazole, oligosaccharides, soybean lecithin, calcium and organic acids, and Abies sibirica and Urtica dioica extracts were also tested. The commercial chitosan formulation was as effective as the practical grade chitosan solutions in the control of gray mold and Rhizopus rot of strawberries immersed in these solutions and kept for 4 days at 20 ± 1 °C. Moreover, the treatment with commercial and experimental resistance inducers reduced gray mold, Rhizopus rot and blue mold of strawberries stored 7 days at 0 ± 1 °C and then exposed to 3 days shelf-life. The highest disease reduction was obtained with the commercial chitosan formulation, followed by benzothiadiazole, calcium and organic acids. The compounds that provided the best results in postharvest applications to control storage decay of strawberries, should be tested in further trials through preharvest treatments, applied at flowering and a few days before harvest.     

Potential of the biopolymer chitosan with different molecular weights to control postharvest gray mold of tomato fruit

Gray mold caused by Botrytis cinerea (Pers.) is the most economically important postharvest disease of fruit and vegetables at harvest and during storage. Therefore the current study was conducted to investigate the effectiveness of chitosan with different molecular weights on gray mold in vitro and in vivo in tomato fruit (Solanum lycopersicum L. var. lycopersicum) stored at different temperatures. In an in vitro experiment, the results demonstrated that the antifungal activity increased as the chitosan molecular weight decreased. In an in vivo study, chitosan treatments significantly reduced fungal decay and all compounds with concentrations of 2000 and 4000 mg/L showed complete control of the fungus in wound-inoculated fruit. Chitosan with a molecular weight of 5.7 × 10⁴ g/mol was the most effective compound among those tested. The results also revealed that high chitosan concentrations correlated with low disease incidence regardless of storage conditions. In addition to the antifungal activity, chitosan had the potential for the elicitation of defense markers, including total soluble phenolic compounds, polyphenoloxidase (PPO) activity and total protein content. Chitosan treatment decreased the activity of PPO and enhanced total protein and phenolic compounds in wounded tomato fruit. These findings suggest that the effects of chitosan with different molecular weights on gray mold in tomato fruit may be associated with direct fungitoxic properties against the pathogen, and the elicitation of biochemical defense responses in fruit.     

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.     

Deployment of low-level ozone-enrichment for the preservation of chilled fresh produce

Tomatoes, strawberries, table grapes and plums were inoculated with Botrytis cinerea (grey mould), transferred to chilled storage (13 °C) and exposed to ‘clean air’ or low-level ozone-enrichment (0.1 μmol mol⁻¹). Ozone-enrichment resulted in a substantial decline in spore production as well as visible lesion development in all treated fruit. Exposure-response studies performed specifically on tomato fruit (exposed to concentrations ranging between 0.005 and 5.0 μmol mol⁻¹ ozone) revealed lesion development and spore production/viability to be markedly reduced in produce exposed to ozone prior to, or following, infection with B. cinerea; higher concentrations/duration of exposure yielding greater reductions in lesion development and spore production/viability. Impacts on Botrytis colonies grown on Potato Dextrose Agar (PDA) for 5–6 days at 13 °C and 95% relative humidity (RH) revealed less effects than studies on fruit inoculated with the pathogen in vivo. Taken as a whole, the results imply that ozone-induced suppression of pathogen development is due, to some extent, to impacts on fruit–pathogen interactions. This work suggests that ozone may constitute a desirable and effective residue-free alternative to traditional postharvest fungicide practices. Data presented illustrate that optimal ozone treatment regimes are likely to be commodity-specific and require detailed investigation before such practices can be contemplated commercially.     

Recent advances on the use of natural and safe alternatives to conventional methods to control postharvest gray mold of table grapes

Gray mold, caused by Botrytis cinerea, is the main postharvest decay of table grapes. It can develop in the vineyard and spread rapidly among berries after harvest, during long distant transport, cold storage and shelf-life. In conventional agriculture, bunches are sprayed with fungicides after flowering, at pre-bunch closure, at veraison, and later, depending on the time of harvest. Harvested bunches are usually stored in the presence of sulfur dioxide. However, the use of synthetic fungicides and of sulfur dioxide is not allowed on organic grapes and the study of alternative methods to control postharvest decay has developed over several decades, along with the demand for safer storage methods. This review summarizes the results published in the field within the last 5 years (2006-2010). We can group these approaches as follows: (i) biocontrol agents; (ii) natural antimicrobials; (iii) GRAS type decontaminating agents; and (iv) physical means. Two biocontrol agents, Muscodor albus and Hanseniaspora uvarum, have shown equal or better effectiveness than conventional methods to control gray mold of table grapes in laboratory scale experiments. Currently, the bottleneck for the commercial use of biocontrol agents is that the registration process is comparable to that of fungicides, with similar costs but often with a narrower market. This delays their transition from experimental to practical use. Natural antimicrobials, such as salts, chitosan, and plant extracts, have demonstrated good results and often have been applied in various scales. Several GRAS-classified sanitizers have been tested to extend postharvest storage of table grapes, including acetic acid, electrolyzed oxidizing water, ozone, and ethanol. Physical technologies involving variations in temperature, UV-C irradiation, pressure or changing atmospheric composition, are all postharvest practices which require significant adaptation by an industry which is accustomed to minimal intervention during harvest. Overall, the use of ozone and of calcium chloride are two promising examples of treatments that are beginning to be adopted on a commercial scale. The requirements for the optimal treatment of grapes against gray mold before harvest or during storage are summarized.     

Effect of postharvest biofumigation on fungal decay,sensory quality,and antioxidant levels of blueberry fruit

Postharvest decay, caused by various fungal pathogens, is an important concern in commercial blueberry production, but current options for managing postharvest diseases are limited for this crop. Four plant essential oils (cinnamon oil, linalool, p-cymene, and peppermint leaf oil) and the plant oil-derived biofungicides Sporan (rosemary and wintergreen oils) and Sporatec (rosemary, clove, and thyme oils) were evaluated as postharvest biofumigants to manage fungal decay under refrigerated holding conditions. Hand-harvested Tifblue rabbiteye blueberry fruit were inoculated at the stem end with conidial suspensions of Alternaria alternata, Botrytis cinerea, Colletotrichum acutatum, or sterile deionized water (check inoculation) and subjected to biofumigation treatments under refrigeration (7 °C) for 1 wk. Sporatec volatiles reduced disease incidence significantly (P < 0.05) in most cases, whereas other treatments had no consistent effect on postharvest decay. Sensory analysis of uninoculated, biofumigated berries was performed utilizing a trained sensory panel, and biofumigation was found to have significant negative impacts on several sensory attributes such as sourness, astringency, juiciness, bitterness, and blueberry-like flavor. Biofumigated fruit were also analyzed for antioxidant capacity and individual anthocyanins, and no consistent effects on these antioxidant-related variables were found in treated berries. Because of limited efficacy in reducing postharvest decay, negative impacts on sensory qualities, and failure to increase antioxidant levels, the potential for postharvest biofumigation of blueberries under refrigerated holding conditions appears limited.     

Pre- and postharvest treatment with alternatives to synthetic fungicides to control postharvest decay of sweet cherry

The effectiveness of alternatives to synthetic fungicides for the control of pathogens causing postharvest diseases of sweet cherry was tested in vitro and in vivo. When amended to potato dextrose-agar, oligosaccharides, benzothiadiazole, chitosan, calcium plus organic acids, and nettle macerate reduced the growth of Monilinia laxa, Botrytis cinerea and Rhizopus stolonifer. Treatment of sweet cherries three days before harvest or soon after harvest with oligosaccharides, benzothiadiazole, chitosan, calcium plus organic acids, nettle extract, fir extract, laminarin, or potassium bicarbonate reduced brown rot, gray mold, Rhizopus rot, Alternaria rot, blue mold and green rot of cherries kept 10 d at 20 ± 1 °C, or 14 d at 0.5 ± 1 °C and then exposed to 7 d of shelf-life at 20 ± 1 °C. Among these resistance inducers, when applied either preharvest or postharvest, chitosan was one of the most effective in reducing storage decay of sweet cherry, and its antimicrobial activity in vitro and in field trials was comparable to that of the fungicide fenhexamid. Benzothiadiazole was more effective when applied postharvest than with preharvest spraying. These resistance inducers could represent good options for organic growers and food companies, or they can complement the use of synthetic fungicides in an integrated disease management strategy.     

Effectiveness of a short hyperbaric treatment to control postharvest decay of sweet cherries and table grapes

The effectiveness of short hyperbaric treatments to control postharvest decay of sweet cherries (Prunus avium L., cv Ferrovia) and table grapes (Vitis vinifera L., cv Italia) was investigated. Sweet cherries and table grape berries were exposed to the pressure of 1140 mmHg (1.5 atm) for 4 and 24 h, respectively, in 64 L gas-proof tanks. Fruit kept at ambient pressure (near 760 mmHg, 1.0 atm) served as a control. Postharvest rots of sweet cherries arose from naturally occurring infections, whereas table grape berries were artificially wounded, exposed to the hyperbaric treatment, then the wounds inoculated with 20 μL of a Botrytis cinerea conidial suspension (5 × 10⁴ spores mL⁻¹). Sweet cherries were stored at 0 ± 1 °C for 14 d, followed by 7 d at 20 ± 1 °C. Table grapes berries were kept at 20 ± 1 °C for 3 d. On sweet cherries, hyperbaric treatment reduced the incidence of brown rot, grey mould, and blue mould, with respect to the control. Similarly, on treated table grapes a significant reduction of lesion diameter and percentage of B. cinerea infected berries was observed. Induced resistance was likely to be responsible for the observed decay reduction. To our knowledge, this is the first report on the effectiveness of short hyperbaric treatments in controlling postharvest decay of sweet cherries and table grapes.