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.     

Calcium chloride extends the keeping quality of fig fruit (Ficus carica L.) during storage and shelf-life

The effects of postharvest application of fruit hardening chemical agents on fig (Ficus carica L. cv. Poona) fruit were compared with untreated figs during storage. The impact of calcium chloride (4%) was notable in terms of retention of fruit color, texture and increased accumulation of ascorbic acid, compared to untreated control figs. Pretreatment with calcium chloride (4%) was found to be most effective in checking the growth of both mesophilic aerobic bacteria and yeast and molds at low temperature (1 ± 0.5 °C; 95–98% RH) storage and it further delayed ripening and senescence of figs and was beneficial in prolonging the postharvest life twofold. Treated figs without microbial spoilage could be used for short term storage, transportation, distribution and marketing for long distance domestic markets in India.     

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

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

Integration of Lactobacillus plantarum A7 with thyme and cumin essential oils as a potential biocontrol tool for gray mold rot on strawberry fruit

Chemical fungicides have been intensively used in the control of postharvest decay in fruit in postharvest conditions; nevertheless, continuous use of these fungicides has faced two major obstacles: development of pathogen resistance to many key fungicides, and public knowledge on the health and environmental hazards of these compounds. This study evaluated the efficacy of Lactobacillus plantarum A7, thyme (Thymus vulgaris L.) and cumin (Cuminum cyminum L.) essential oils and the combination of these three elements as postharvest biocontrol agents against Botrytis spp. on strawberry fruit. Thyme oil had a remarkable antifungal effect against Botrytis spp. in vitro, whereas an inhibitory effect of cumin oil was achieved in higher concentrations. With thyme oil (2 h after artificial inoculation of the fruit), among three tested concentrations, only the 200 μL/L concentration showed an inhibitory effect on strawberries against Botrytis spp. (91.97%), while higher concentrations of cumin oil were required to prevent decay significantly. Both combinations of L. plantarum+ cumin oil and L. plantarum+ thyme oil completely inhibited the mycelia growth of the pathogens in vitro. Results showed that the combined treatments of strawberry fruit with L. plantarum+ cumin oil (50 μL/L) and L. plantarum+ thyme oil (100 μL/L) resulted in remarkably improved control of Botrytis infections, in comparison to the stand-alone application of L. plantarum A7 or essential oils. Quality (i.e. pH, acidity and ascorbic acid content) and sensory attributes of the strawberry fruit were better in the case of using cumin compared to thyme oil, when a combination of L. plantarum A7 and essential oils was used. This study has demonstrated that the integration of L. plantarum A7 with thyme and cumin essential oils is a potential biocontrol tool as a biofungicide in postharvest stage.     

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.     

Postharvest ethylene conditioning as a tool to reduce quality loss of stored mature sweet oranges

Ethylene is related to senescence but also induces protective mechanisms against stress in plants. The citrus industry only applies the hormone to induce fruit degreening. The aim of this work was to determine the effect of ethylene on the quality of colored citrus fruit stored under commercial conditions to extend postharvest life, since it protects them from stress causing postharvest disorders such as chilling injury (CI) and non-chilling peel pitting (NCPP). The effect of conditioning mature Navelate and Lane Late sweet oranges (Citrus sinensis L. Osbeck) for 4 days with 2 μL L⁻¹ ethylene at 12 °C, rather than at higher temperatures used for degreening, on the quality of fruit stored at 2 or 12 °C, was examined. The ethylene conditioning (EC) treatment did not increase color but reduced calyx abscission and NCPP in fruit of both cultivars stored at 12 °C, and also CI in Navelate fruit at 2 °C. Lane Late fruit did not develop CI but showed a new disorder in EC fruit held at 2 °C. This disorder began as scalded areas around the fruit stem end and extended over the fruit surface during storage. EC had no deleterious effect on the quality of Navelate oranges stored at either 2 or 12 °C. Similar results were found in Lane Late fruit although EC slightly increased off-flavor perception at 2 °C and the maturity index at 2 and 12 °C. Moreover, EC slightly increased the content of bioactive flavonoids in the pulp of Navelate fruit but significant differences between control and EC fruit were only found after prolonged storage at 2 °C. In Lane Late fruit, EC avoided the initial decrease in flavonoid content found in control samples. Results show, therefore, that EC at 12 °C may be a tool to extend postharvest life of NCPP and CI-sensitive oranges, and that the tolerance of citrus cultivars to the combined effect of EC and non-freezing low temperature (2 °C) should be tested to select the proper storage temperature.     

Integration of pre- and postharvest treatments for the control of black spot caused by Alternaria alternata in stored persimmon fruit

In Israel, black spot caused by Alternaria alternata is the main postharvest factor that impairs the quality and reduces the storability of persimmon fruit (Diospyros kaki cv. Triumph). The fungus infects the fruit in the orchard and remains quiescent until harvest. After harvest, the pathogen slowly colonizes the fruit during storage at 0 °C, which elicits black spot symptom development 2–3 months after storage entry. A commercial postharvest dip treatment in chlorine at 500 mg L^?1, released from sodium troclosene tablets, effectively controlled black spot in fruit stored for up to 2 months. However, decay incidence increased as the length of storage was extended beyond 2.5 months. The long incubation period that precedes black spot symptom development after harvest enabled the development of a series of integrative approaches for application at the pre- and postharvest stages, in combination with the commercial chlorine dip treatment, to improve the control of black spot disease. Preharvest treatments included treatment with the cytokinin-like N₁-(2-chloro-4-pyridyl)-N₃-phenylurea (CPPU) 30 d after fruit set, or a single spray with the curative fungicide polyoxin B 14 d before harvest, and when one of these was applied in combination with the postharvest chlorine dip treatment, the black spot infected area was reduced by 3 and 60%, respectively, compared with the chlorine dip alone. At the postharvest stage, fogging during storage, or post-storage on-line spraying with sodium troclosene, when applied in combination with the postharvest chlorine dip, improved the percentage of marketable fruit by 2 or 10%, respectively, compared with the chlorine dip alone. The results indicate that postharvest pathogens that show a slow colonization pattern might enable the integration of pre- and postharvest disease control methods to improve quality and reduce postharvest disease development.     

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.     

Methyl jasmonate induces resistance against Penicillium citrinum in Chinese bayberry by priming of defense responses

Methyl jasmonate (MeJA) can act as an activator of defense responses in plants against pathogenic infection. However, the mechanisms involved in the postharvest induction of resistance by MeJA in fruit are largely unknown. Thus, we investigated the effect of a postharvest MeJA treatment on disease resistance against Penicillium citrinum infection in Chinese bayberries and the possible mechanisms. The results indicated that treatment with 10 μmol L⁻¹ of MeJA significantly inhibited green mould rot caused by P. citrinum, with the decay incidence being 66.2% lower than that of the control fruit after storage at 1 °C for 8 d. Moreover, it is clear that MeJA triggers a priming mechanism in Chinese bayberries, since only the MeJA-treated fruit showed an enhanced capacity to augment defense responses upon challenge with the pathogen. These augmented responses included an H₂O₂ burst, enhanced protein levels of phenylalanine ammonia-lyase and chitinase, and accumulation of phenolic compounds, lignin and phytoalexin. Therefore, our results suggest that a postharvest MeJA treatment induces disease resistance against P. citrinum in Chinese bayberries by priming of defense responses.     

UV-B irradiation retards chlorophyll degradation in lime (Citrus latifolia Tan.) fruit

Peel yellowing is a major postharvest problem of lime fruit. Research was conducted to control peel yellowing by UV-B irradiation. Mature green lime fruit were irradiated with UV-B doses at 0 (control), 8.8, and 13.2 kJ m^?2 and then stored at 25 °C in darkness. UV-B treatment at 8.8 kJ m^?2 efficiently delayed the decrease of chlorophyll content. A high level of chlorophyllide a accumulated in mature green fruit and then gradually decreased with the progress of peel yellowing. The chlorophyllide a level was higher in 8.8 kJ m^?2 UV-B-treated fruit than it was in the controls. The pheophorbide a level declined in lime fruit treated with 8.8 kJ m^?2 UV-B, especially during the development of yellowing. In addition, the pheophytin a level increased by 8.8 kJ m^?2 UV-B treatment at the late period of storage. We concluded that UV-B treatment effectively suppressed chlorophyll degradation in mature green lime during storage, which suggests that UV-B irradiation is a usable method for prolonging the postharvest life of lime fruit.     

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.     

Low temperature phosphine fumigation for postharvest control of Liriomyza huidobrensis Blanchard (Diptera: Agromyzidae) on carnation

Phosphine (PH₃) fumigation with different concentrations and exposure durations at low temperature was studied to determine its effects on Liriomyza huidobrensis Blanchard (Diptera: Agromyzidae) on carnations, and on postharvest quality. Laboratory tests showed that tolerance of L. huidobrensis to phosphine fumigation at 5 °C varied with different life stages. 1 d-old eggs and adults showed the highest susceptibility, and 3 d-old eggs was the most tolerant stage. In the fumigation tests of 3 d-old eggs with a range of phosphine concentrations from 0.46 to 2.73 mg L⁻¹ and exposure durations from 6 to 144 h at 5 °C, 85.96–282.08 h fumigation durations were required to achieve 99% mortality with different phosphine concentrations. The expression of C^0.77T = k was obtained, which indicated that exposure duration other than phosphine concentration was the critical factor in the toxicity of phosphine against the 3 d-old eggs of L. huidobrensis. Controlled atmosphere (CA) treatment with increased CO₂ and reduced O₂ had synergistic effects on phosphine toxicity. Phosphine fumigation could achieve 100% mortality for insects of L. huidobrensis on carnation, and had no significant adverse effects on vase life and damage indices of carnation at 1.92 mg L⁻¹ PH₃ and 8% CO₂ for 32 h, and at 3.44 mg L⁻¹ for 3 d at 5 °C. All results suggested that phosphine fumigation at low temperature could be used as an alternative for postharvest control of L. huidobrensis on carnations.     

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.     

Pre-storage hypobaric treatments delay fungal decay of strawberries

Fungal decay is a major cause of postharvest losses in strawberries. The traditional approach for controlling fungal decay is the use of fungicides. However, the use of fungicides has been questioned as a sustainable and safe method, and is also prohibited in many countries. One potential physical method for reducing fungal decay is application of a short-term hypobaric treatment prior to storage. In this study efficacy of postharvest hypobaric treatments to control natural rot development in strawberries was evaluated. Strawberries were treated with hypobaric pressures (25 kPa_a, 50 kPa_a and 75 kPa_a) for 4 h at 20 °C and subsequently stored at 20 °C or 5 °C. A 50 kPa_a treatment consistently delayed rot development in samples stored at either temperature confirming that the technique has potential as a non-chemical treatment. Moreover 50 kPa_a treatments did not affect weight loss and firmness at either 20 °C or 5 °C. An initial increase in respiration rate was observed in 50 kPa_a treated samples potentially indicating mild stress due to hypobaric treatment. An in vitro fungal study found that 50 kPa_a treatment for 4 h did not affect the rate of radial growth of colonies of Botrytis cinerea and Rhizopus stolonifer, providing further evidence that the potential mechanism of hypobaric treatment is induction of the defence system within the fruit rather than a direct effect on fungal viability. Further molecular and biochemical research is required to evaluate the possible stimulation of resistance in fruit through short-term 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.     

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.     

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).     

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.     

Ripening behavior and quality of modified atmosphere packed ‘Doyenne du Comice’ pears during cold storage and simulated transit

The effect of MAP on extending storage life and maintaining fruit quality was studied in ‘Doyenne du Comice’ (Pyrus communis L.) pears at Hood River and Medford, Oregon. Control fruit packed in standard perforated polyethylene liners started to show senescent core breakdown and lost the capacity to ripen at 20 °C after 4–5 months of cold storage in Hood River and after 5.25–6 months in Medford. LifeSpan^® L257 MAP achieved steady-state atmospheres of 15.8% O₂ + 3.7% CO₂ in Hood River and 15.7–17.5% O₂ + 3.8–5.7% CO₂ in Medford. MAP inhibited ethylene production, ascorbic acid degradation and malondialdehyde accumulation, and extended storage life for up to 6 months with maintenance of fruit flesh firmness (FF) and skin color without commercially unacceptable level of physiological disorders. After 4, 5 and 6 months at −1 °C, MAP fruit exhibited climacteric-like patterns of ethylene production and softened to proper texture with desirable eating quality on day 5 during ripening at 20 °C. After 6 months at −1 °C plus 2 weeks of simulated transit conditions, MAP fruit maintained FF and skin color and had good eating quality at transit temperatures of 2 and 4.5 °C (10.1–11.5% O₂ + 4.8–5.2% CO₂), but reduced FF substantially and developed internal browning disorder at 7.5 and 20 °C (3.2–7.2% O₂ + 7.9–9.5% CO₂). The storage life of ‘Doyenne du Comice’ pears with high eating quality could be increased by up to 2 months when packed in MAP as compared with fruit packed in standard perforated polyethylene liners.     

Combination of peracetic acid and hot water treatment to control postharvest brown rot on peaches and nectarines

Brown rot caused by Monilinia spp. is the most important postharvest disease of stone fruit. From preliminary studies, the combination of 0.25% hydrogen peroxide, 0.02% peracetic acid (PAA) and 0.075% acetic acid, corresponding to 300 mg L⁻¹ of PAA, was selected to control Monilinia fructicola. Brown rot control was similarly controlled when the same concentration of PAA was applied with a PAA-based commercial product. In order to reduce PAA concentration, combinations of different concentrations and temperatures were evaluated. A treatment of 200 mg L⁻¹ of PAA at 40 °C for 40 s was selected to control pre-existing and future infections, different inoculum concentrations of M. fructicola and to control brown rot on naturally infected fruit. Brown rot was completely controlled with the selected treatment when peaches and nectarines were inoculated 0 h before the treatment but it was not controlled when infection time was increased to 24, 48 and 72 h. Also, the treatment significantly controlled brown rot at all inoculum concentrations evaluated (10³, 10⁴, 10⁵ and 10⁶ conidia mL⁻¹) in both peaches and nectarines, but no protection against future infections was observed. In naturally infected fruit, brown rot incidence was slightly but significantly reduced to 61 and 36% in ‘Roig d’Albesa’ and ‘Placido’ peaches, respectively, but not in nectarines. Immersion for 40 s in 200 mg L⁻¹ of PAA at 40 °C provides an alternative treatment to control only recent infections of Monilinia spp. whatever their concentration without generally affecting fruit quality.