Hypobaric treatment stimulates defence-related enzymes in strawberry

Strawberry fruit are very prone to fungal decay. Postharvest hypobaric treatment is a potential new technique to delay fungal decay in strawberries. Hypobaric treated (50 kPa, 4 h) strawberries had reduced rot incidence from natural infection during subsequent storage for 4 days at 20 °C and after subsequent inoculation with Botrytis cinerea or Rhizopus stolonifer spores. Biochemical analysis of strawberries suggested that activities of defence-related enzymes were increased with the hypobaric treatment; phenylalanine ammonia-lyase (PAL, EC: 4.3.1.24) and chitinase (EC: 3.2.1.14) peaked 12 h after treatment, while peroxidase (POD, EC: 1.11.1.7) increased immediately. Polyphenol oxidase (PPO, EC: 1.10.3.1) activity remained unaffected during subsequent storage for 48 h at 20 °C. In addition, the effect of low oxygen treatment (10% at 101 kPa, 4 h) was investigated to determine if the lower partial pressure of oxygen generated during hypobaric treatment contributed to the observed effect. However the low oxygen treatment did not influence rot development, suggesting that the treatment effects were pressure rather than oxygen related. The results suggest that hypobaric treatment causes reduced decay incidence due to stimulation of defence-related enzymes. Studies of defence-related genes are required to further explore the induced resistance mechanisms of hypobaric treatments.     

Control of postharvest grey mould (Botrytis cinerea Per.: Fr.) on strawberries by glucosinolate-derived allyl-isothiocyanate treatments

The vapours of allyl-isothiocyanate (AITC) were evaluated in in vitro and in vivo trials against Botrytis cinerea, a severe pathogen of strawberries. In in vitro trials AITC activity was assayed on conidial germination and mycelial growth of the fungus. The mycelium appeared less sensitive to AITC than conidia (EC₅₀ values of 1.35 mg L⁻¹ and 0.62 mg L⁻¹, respectively). In addition, AITC had a fungistatic effect against the pathogen, since the values of EC₅₀, for both parameters, increased by around 30% after AITC removal. In in vivo trials, ‘Tecla’ and ‘Monterey’ strawberries (spring-bearing and day-neutral cultivars, respectively) obtained from organic production and naturally infected by B. Cinerea, were exposed for 4 h in an atmosphere enriched by pure AITC or derived from defatted seed meals of Brassica carinata (0.1 mg L⁻¹, in a 0.1 m³ treatment cabinet). After 2 days at 0 °C and another 3–4 days at 20 °C, the fruit were evaluated for grey mould infections. The AITC treatment reduced the decay caused by the pathogen by over 47.4% up to 91.5%, significantly different from the untreated fruit. No significant differences were found between synthetic and glucosinolate-derived AITC. Residue analysis performed on fruit at the end of storage (7 d after treatment) showed values lower than 1 mg kg⁻¹. Total phenolic content and antioxidant capacity estimated in treated and untreated strawberries showed no significant difference between control and AITC treated fruit. Our results show it is possible to reduce the incidence of postharvest grey mould on strawberries with a treatment of AITC (0.1 mg L⁻¹) for 4 h, opening a potential application of biofumigation in the postharvest control of B. cinerea in strawberry.     

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.     

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.     

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.     

Evaluation of the use of sulfur dioxide to reduce postharvest losses on dark and green figs

Postharvest diseases limit the storage period and market life of fresh figs (Ficus carica L.). The objective of this work was to determine the effect of sulfur dioxide (SO₂) applied by fumigation and/or by dual release SO₂ generating pads on postharvest decay and quality retention of ‘Black Mission’ and ‘Brown Turkey’ (dark skin), and ‘Kadota’ and ‘Sierra’ (green skin) figs. A protocol for the computer-controlled application of gaseous SO₂ has been developed which allows the application of very low specific concentration × time products of SO₂ and simultaneous monitoring of the application progress. In vitro tests with important fungal, yeast and bacterial postharvest pathogens plated on Petri dishes and exposed to a SO₂ concentration × time product (C × t) of 100 (μL/L) h at different temperatures showed fewer survived at 20 °C than at 0 °C. Therefore, fumigations were carried out at 20 °C in the rest of the experiments. The evaluation of different SO₂ concentration × time products showed that a product of 25 (μL/L) h provided the best compromise between decay control and fruit injury. The performance of SO₂ fumigations on warm or cold fruit, its combination with SO₂ generating pads, and the use of repeated fumigations during cold storage were also evaluated. All the SO₂ treatments tested reduced the percentage of decay, extending the market life of fresh figs. However, in some cases, the use of SO₂ generating pads increased the incidence of skin bleaching. Fumigation of warm fruit at 25 (μL/L) h of SO₂ reduced populations of Alternaria and Rhizopus spp. growing on the fig surface. The treatment was more effective against Rhizopus spp. than against Alternaria spp. Contamination of fruit by Botrytis spp. and Penicillium spp. was also reduced by SO₂. In conclusion, results showed that SO₂ can be a potential tool to control postharvest rots and therefore increase the market life of fresh figs.     

Combination of hot water,Bacillus amyloliquefaciens HF-01 and sodium bicarbonate treatments to control postharvest decay of mandarin fruit

An antagonistic isolate Bacillus amyloliquefaciens HF-01, sodium bicarbonate (SBC) and hot water treatment (HW) were investigated individually and in combination against green and blue mold and sour rot caused by Penicillium digitatum, P. italicum and Geotrichum citri-aurantii respectively, in mandarin fruit. Populations of antagonists were stable in the presence of 1% or 2% SBC treatment, and spore germination of pathogens in potato dextrose broth was greatly controlled by the hot water treatment of 45 °C for 2 min. Individual application of sodium bicarbonate at low rates and hot water treatment, although reducing disease incidence after 8 weeks or 4 weeks of storage at 6 °C or 25 °C respectively, was not as effective as the fungicide treatment. The treatment comprising B. amyloliquefaciens combined with 2% SBC or/and HW (45 °C for 2 min) was as effective as the fungicide treatment and reduced decay to less than 80% compared to the control. B. amyloliquefaciens HF-01 alone or in combination with 2% SBC or/and HW significantly reduced postharvest decay without impairing fruit quality after storage at 25 °C for 4 weeks or at 6 °C for 8 weeks. These results suggest that the combination of B. amyloliquefaciens HF-01, SBC and HW could be a promising method for the control of postharvest decay on citrus while maintaining fruit quality after harvest.     

Increasing strawberry shelf-life with carvacrol and methyl cinnamate antimicrobial vapors released from edible films

The effect of carvacrol and methyl cinnamate vapors incorporated into strawberry puree edible films on the postharvest quality of strawberry fruit (Fragaria × ananassa) was investigated. Fresh strawberries were packed in clamshells and kept at 10 °C for 10 days with 90% RH. Strawberry puree edible films, applied in the clamshell, served as carriers for the controlled release of natural antimicrobial compounds without direct contact with the fruit. Changes in weight loss, visible decay, firmness, surface color, total soluble solids content, total soluble phenolics content and antioxidant capacity of strawberries during storage were evaluated. A significant delay and reduction in the severity of visible decay was observed in fruit exposed to antimicrobial vapors. Carvacrol and methyl cinnamate vapors released from the films helped to maintain firmness and brightness of strawberries as compare to the untreated strawberries. The natural antimicrobial vapors also increased the total soluble phenolics content and antioxidant activity of fruit at the end of the storage period.     

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

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

Can hot water treatments enhance or maintain postharvest quality of spinach leaves?

It has been reported that a short duration hot water treatment, applied as a heat shock, improves subsequent postharvest quality in bagged spinach and rocket leaves. This study has established that the maximum hot water temperature and duration before spinach leaves showed damage, was 45 °C for 60 s. Subsequent detailed studies compared postharvest quality of leaves treated at 45 °C for 60 s immediately after harvest with untreated leaves after 5 and 10 days of storage at 4 °C. Heated leaves were significantly lighter and more yellow suggesting enhanced senescence, but leaf membrane integrity and associated gas composition of the storage atmosphere were not significantly different. Hot water treatment at 45 °C for 60 s applied immediately after harvest had a mixed effect on the biochemical constituents of the leaves; total carotenoid concentration was maintained compared to untreated leaves but the contents of ascorbic acid, dehydroascorbic acid, chlorophyll a and b were not affected. These observations suggest that in contrast to other reports, hot water treatments have limited commercial potential for postharvest quality improvement of spinach leaves.     

Effect of calcium dips and chitosan coatings on postharvest life of strawberries (Fragaria x ananassa)

Strawberries (Fragaria x ananassa Duch.) were treated either with 1% calcium gluconate dips, 1.5% chitosan coatings or with a coating formulation containing 1.5% chitosan + 1% calcium gluconate and stored at 20 °C for up to 4 days. The effectiveness of the treatments was assessed by evaluating their impact on the following parameters: fungal decay incidence, loss of weight, firmness, external color, pH, titratable acidity and soluble solids content. Calcium dips were effective in decreasing surface damage and delaying both fungal decay and loss of firmness compared to untreated fruit. No sign of fungal decay was observed in fruit coated with 1.5% chitosan which also reduced fruit weight loss. Chitosan coatings markedly slowed the ripening of strawberries as shown by their retention of firmness and delayed changes in their external color. To a lesser extent titratable acidity and pH were also affected by coatings. Whilst addition of calcium gluconate to the chitosan coating formulation did not further extend the shelf-life of the fruit, the amount of calcium retained by strawberries was greater than that obtained with calcium dips alone, thus resulting in increased nutritional value of the strawberries.     

Hot water dipping treatments on Tarocco orange fruit and their effects on peel essential oil

The most common and serious diseases which affect citrus fruit after harvest in Italy are induced by Penicillium digitatum Sacc. and Penicillium italicum Weh., responsible respectively for green and blue mold rots. This paper deals with the effectiveness of hot water dipping (HWD) treatments as alternative means to control postharvest decay on Tarocco orange fruit [Citrus sinensis (L.) Osbeck], and their effect on fruit quality with special regard to peel essential oils. Selected treatments were HWD at 52 °C for 180 s and at 56 °C for 20 s. These treatments were compared with an effective fungicide standard treatment (Imazalil) and an untreated control. The results showed that HWD at 56 °C for 20 s was more effective in inhibiting P. digitatum spore germination than HWD at 52 °C for longer exposure time. In addition, HWD treatment at 56 °C significantly increased the level of alcohols, esters and aliphatic (fatty) aldehydes. Therefore, the lowest values of decay incidence recorded in HWD fruit treated at 56 °C may be due to the increase in oxygenated monoterpenes, esters and aldehydes. Finally, HWD treatments did not cause surface damage or color change and did not influence internal quality parameters.     

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.     

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.     

Cold quarantine responses of ‘Tarocco’ oranges to short hot water and thiabendazole postharvest dip treatments

This study investigated the effects of brief hot water and thiabendazole (TBZ) postharvest dip treatments on ultrastructural changes of fruit epicuticular wax (ECW), TBZ residues, decay development and quality traits of ‘Tarocco’ oranges [Citrus sinensis (L.) Osbek] subjected to cold quarantine, subsequent simulated transport and shelf-life. Commercially mature fruit were submerged in water at 20 °C (control fruit) or TBZ at 1000 mg/L and 20 °C for 60 s, or in hot water without or with TBZ at 300 mg/L and 53, 56, or 59 °C for 60, 30, and 15 s respectively. Following treatments, fruit were stored for 3 weeks at 1 °C (simulated quarantine conditions for fruit disinfestations against Mediterranean fruit fly, Medfly), followed by 4 days at 3 °C (simulated long distance transport), and finally kept at 20 °C for 3 days (shelf-life, SL). Scanning electron microscopy (SEM) analysis of ‘Tarocco’ orange surface showed that the typical wax platelets, lifting around edges of wax plates and areas free of epicuticular wax (ECW), that disappeared after hot water dips at 53–59 °C for 60–15 s, become visible again after storage for 21 days at 1 °C (quarantine conditions), and changes involving the appearance of rough ultrastructure, presence large curled plates, fissured wax crusts, and areas with ECW deficiencies, became much more pronounced after shelf-life. These occurrences were related to the transient effect of hot water treatment in decay control. Conversely, treatments with 300 mg/L TBZ 53 °C for 60 s or 56 °C for 30 s effectively reduced decay after quarantine. These treatments were as effective as standard treatment with 1000 mg/L TBZ at 20 °C and produced similar TBZ residue levels in fruit, without impairing fruit quality traits such as visual appearance, weight loss, compression test, sensory attributes, juice color parameters (a*, b*, h, L*, and Chroma), and juice chemical characteristics (soluble solids content, titratable acidity, ascorbic acid, glucose, sucrose, citric acid, total phenols, total anthocyanins, and total antioxidant activity).     

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.     

Evaluation of postharvest treatments with chemical resistance inducers to control green and blue molds on orange fruit

Preventive and curative activities of postharvest treatments with selected chemical resistance inducers to control postharvest green (GM) and blue (BM) molds on oranges (cvs. ‘Valencia’ or ‘Lanelate’) artificially inoculated with Penicillium digitatum and Penicillium italicum, respectively, were evaluated. In vivo primary screenings to select the most effective chemicals and concentrations were performed with benzothiadiazole (BTH), β-aminobutyric acid (BABA), 2,6-dichloroisonicotinic acid (INA), sodium silicate (SSi), salicylic acid (SA), acetylsalicylic acid (ASA) and harpin. INA at 0.03 mM, SA at 0.25 mM, BABA at 0.3 mM and BTH at 0.9 mM were selected and tested afterwards as dips at 20 °C for 60 or 150 s with oranges artificially inoculated before or after the treatment and incubated for 7 d at 20 °C. Although it was an effective treatment, SSi at 1000 mM was discarded because of potential phytotoxicity to the fruit rind. Preventive or curative postharvest dips at room temperature had no effect or only reduced the development of GM and BM very slightly. Therefore, these treatments cannot be recommended for inclusion in postharvest decay management programs for citrus packinghouses.     

Effects of gamma and UV-C irradiation on the postharvest control of papaya anthracnose

Anthracnose is the main postharvest disease in papaya fruit. Today, there is considerable interest on alternative methods of control to promote resistance against pathogens and supplement or replace the use of fungicides. The goal of this work was to evaluate the effects of gamma and UV-C irradiation on Colletotrichum gloeosporioides, the causal agent of anthracnose. Mycelial growth, sporulation, and conidial germination were evaluated in vitro after fungal exposition to different irradiation doses. In the in vivo assays, ‘Golden’ papaya fruit were inoculated through subcuticular injections of a conidial suspension or mycelium discs. Next, fruit were submitted to different irradiation doses (0, 0.12, 0.25, 0.5, 0.75, and 1 kGy), using Co⁶⁰ as source, or UV-C (0, 0.2, 0.4, 0.84, 1.3, and 2.4 kJ m⁻²). To check the possibility of resistance induction by irradiation, papayas were also inoculated 24, 48, or 72 h after the treatments. The fruit were stored at 25 °C/80% RH for 7 days and evaluated for incidence and rot severity. The results showed that the 0.75 and 1 kGy doses inhibited conidial germination and mycelial growth in vitro. All doses increased fungal sporulation. The 0.75 and 1 kGy doses reduced anthracnose incidence and severity, but did not reduce them when the fruit were inoculated after irradiation. All UV-C doses inhibited conidial germination and those higher than 0.84 kJ m⁻² inhibited mycelial growth. The 0.4, 0.84, and 1.3 kJ m⁻² UV-C doses reduced fungal sporulation in vitro. There was no effect of UV-C doses and time intervals between treatment and inoculation on anthracnose control and fungal sporulation in fruit lesions. Moreover, all UV-C doses caused scald on the fruit. Thus, gamma irradiation can contribute for the reduction of postharvest losses caused by anthracnose and reduce the use or doses of fungicides on disease control.     

Effects of X-ray irradiation and sodium carbonate treatments on postharvest Penicillium decay and quality attributes of clementine mandarins

The integration of sodium carbonate (SC; dips at 20 °C for 150 s in aqueous 3% SC solutions) treatments and X-ray irradiation (at doses of 510 and 875 Gy) was evaluated on artificially inoculated ‘Clemenules’ clementine mandarins for the control of postharvest green and blue molds, caused by Penicillium digitatum and Penicillium italicum, respectively. Although significant, the reduction of both disease incidence (number of infected fruit) and severity (lesion diameter) on fruit either incubated at 20 °C for 7 days or cold-stored at 5 °C for 21 days was not sufficient for satisfactory disease control under hypothetical commercial conditions. Therefore, the combined treatments could not be a substitute for conventional chemical fungicides. However, pathogen sporulation was greatly inhibited on infected clementines, thus X-irradiation could be of value for management of Penicillium resistant strains and to reduce inoculum levels in citrus packinghouses. X-ray irradiation at 195, 395, 510, and 875 Gy did not influence either decay incidence or the area under the disease progress curve (AUDPC) of lesions of green and blue molds on mandarins inoculated with the pathogens 2, 3, or 6 days after irradiation and incubated for 7 days at 20 °C. Therefore, X-ray treatment did not induce disease resistance in the rind of irradiated fruit. Although X-irradiation at doses up to 875 Gy followed by either 14 days at 20 °C or 60 days at 5 °C caused very slight rind pitting, minor decreases in fruit firmness, and modest increases in juice acetaldehyde and ethanol contents, these changes had no practical impact on fruit quality. Rind color, titratable acidity, soluble solids concentration, maturity index and juice yield were not influenced by irradiation. ‘Clemenules’ can be considered as a clementine cultivar highly tolerant to X-irradiation.     

Edible coatings containing chitosan and moderate modified atmospheres maintain quality and enhance phytochemicals of carrot sticks

Carrot sticks are increasingly in demand as ready-to-eat products, with a major quality problem in the development of white discoloration. Modified atmosphere packaging (MAP) and edible coating have been proposed as postharvest treatments to maintain quality and prolong shelf-life. The combined application of an edible coating containing 5 mL L^?1 of chitosan under two different MAP conditions (10 kPa O₂ + 10 kPa CO₂ in Pack A and 2 kPa O₂ + 15–25 kPa CO₂ in Pack B) over 12 d at 4 °C was studied. Respiration rate, microbial and sensory qualities as well as the contents of vitamin C, carotenoids and phenolics of coated and uncoated carrot sticks were evaluated. The use of the edible coating containing chitosan preserved the overall visual quality and reduced surface whiteness during storage. Microbial populations were very low and not influenced by coating or MAP. Edible coating increased respiration rates of carrot sticks, although this was only noticeable in the package with the less permeable film (Pack B). Vitamin C and carotenoids decreased during storage particularly in coated carrot sticks. In contrast, the content of total phenolics markedly increased in coated carrot sticks stored under moderate O₂ and CO₂ levels, while it was controlled under low O₂ and high CO₂ levels. The combined application of edible coating containing chitosan and moderate O₂ and CO₂ levels maintained quality and enhanced phenolic content in carrot sticks.