Effects of phosphine fumigation on postharvest quality of four Chinese cut flower species

Chrysanthemum (White, Yellow, and Daisy), carnation (Master and Barbara), rose (Carola, Black magic, Diana, Champagne, and Avalanche), and Chinese rose (Golden Medallion, Diplomat, Marina, and Athena) are the main Chinese cut flower species produced for exportation. Cut flowers infested with quarantine pests need methyl bromide (MB) fumigation to satisfy phytosanitary requirements of importing countries. Phosphine (PH₃) is a potential alternative to methyl bromide. Development of phosphine as a phytosanitary treatment requires information regarding its phytotoxicity to cut flowers. Therefore phosphine fumigation at 24 °C and 2 °C was investigated to evaluate its effects on the postharvest quality of cut flowers. Phosphine fumigation for 6 h with dosages as high as 12.2 mg L⁻¹ at 24 °C produced no adverse effects on flower color, diameter, vase life, and other damage indices (DI) for all cultivars. However, different adverse effects on some cultivars were observed after 12 d fumigation at 2 °C. There were significant changes for color values of Carola, Black magic, Diana, Champagne, Avalanche, and Diplomat; significant decrease in flower diameter and vase life of Diana, Champagne, and Avalanche at 3.04 mg L⁻¹, white Chrysanthemum and Diploma at 1.52 and 3.04 mg L⁻¹; significant increase in DI of Champagne and Avalanche at 3.04 mg L⁻¹, and White chrysanthemum, Diana, and Diploma at 1.52 and 3.04 mg L⁻¹. In combination with information on phosphine toxicity to insect pests at ambient and low temperatures in the literature, it is suggested that phosphine fumigation could be a viable replacement of MB fumigation for quarantine treatment of these four cut flower species.     

Characterization of sensitivity of grove and packing house isolates of Penicillium digitatum to pyrimethanil

In most northeast Argentinean citrus packing houses, postharvest fungicide treatments are based on the use of thiabendazole and imazalil. However, these fungicides have been used in a manner highly conducive to the selection and proliferation of resistant biotypes of Penicillium digitatum, the main fruit decay fungus in the area. Recently, a new fungicide, pyrimethanil (PYR), was introduced to control molds. Aims of this study were to determine the baseline sensitivities for PYR against isolates of P. digitatum considering its use in the region is not yet widespread and to evaluate the control of the fungus in vivo. One hundred and nine (109) P. digitatum isolates were collected from diseased fruit within citrus groves (43 isolates) and packing houses (66 isolates). EC₅₀ was determined for each isolate by measuring colony diameters on different agar dilutions of the fungicide. The mean EC₅₀ value of the green mold isolates collected from the groves was 0.14 ± 0.03 mg L⁻¹ while the mean EC₅₀ of those collected from packing houses was 0.13 ± 0.05 mg L⁻¹. No resistant isolates were found in the field where the fungicide is not used, while one isolate originated from a packing house showed an EC₅₀ of 3.40 mg L⁻¹, 26-fold higher than the mean level. This isolate was collected from lemons stored in cool rooms of a packing house where PYR had not been used. Fruit decay by sensitive isolates was reduced approximately 80% by PYR applied at 500–600 mg L⁻¹ by immersion for 60 s at room temperature to inoculated oranges and mandarins. In contrast, the resistant isolate was not controlled by PYR applied at 1000 mg L⁻¹. Thus, the introduction of PYR applied into packing houses should be done carefully and control strategies should be implemented in order to minimize the development of resistant isolates.     

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.     

Impact of a decontamination step with peroxyacetic acid on the shelf-life,sensory quality and nutrient content of grated carrots packed under equilibrium modified atmosphere and stored at 7 °C

Peroxyacetic acid (PAA) is a strong oxidizer and exerts antimicrobial properties. The effect of a decontamination step with 80 and 250 mg L⁻¹ PAA on shelf-life of grated carrots stored under equilibrium modified atmospheric packaging at 7 °C was determined and compared with the shelf-life of unwashed and water-washed carrots. Microbial parameters, including total aerobic plate count, numbers of lactic acid bacteria, Lactobacillae and yeasts, and sensory quality were evaluated. Next to these parameters, atmospheric gas composition, pH and nutrient content were also monitored. The suggested packaging configuration prevented CO₂ accumulation, but at the end of the study anoxic conditions were reached for unwashed carrots and carrots washed with 80 mg L⁻¹ PAA. The microbial shelf-life of water-washed carrots was 4 d based on the yeast count, whereas the flavour was not acceptable after 5 d. The total aerobic plate count and the yeast count determined the shelf-life of carrots treated with 80 mg L⁻¹ PAA on 5 d, whereas the flavour was unacceptable after 7 d. None of the microbial parameters determined the shelf-life of carrots washed with 250 mg L⁻¹ PAA. However, this treatment had already a pronounced adverse effect on the initial sensory quality. Water washing already decreased the content of all individually studied nutrients (−16 to −28%), except for lutein content and the antioxidant capacity. Additional losses after adding PAA on day 0 were found for α-tocopherol and phenols. Regardless of the applied treatment, α- and β-carotene remained stable during storage, whereas ζ-carotene, lutein and α-tocopherol were unstable. The phenol content and the antioxidant capacity of unwashed, water-washed and 80 mg L⁻¹ PAA-treated carrots increased significantly at the end of the storage period, whereas no changes were found in carrots treated with 250 mg L⁻¹ PAA.On the condition that carrots were packed under an adequate EMA, the 80 mg L⁻¹ PAA treatment showed possibilities for extending shelf-life without pronounced effects on nutrient content.     

Essential oils and silver nanoparticles (SNP) as novel agents to extend vase-life of gerbera (Gerbera jamesonii cv. ‘Dune’) flowers

The aim of this study was to evaluate the efficacy of silver nanoparticles (SNP) and essential oils as novel antimicrobial agents in extending the vase-life of gerbera (Gerbera jamesonii cv. ‘Dune’) flowers. The vase-life of flowers held in a solution containing 5 mg L⁻¹ SNP plus 6% sucrose was found to be significantly higher than with 8-HQC (8-hydroxyquinoline citrate) or control treatments. However, the vase-life was not different to that of flowers held in similar concentrations of silver nitrate. All gerbera flowers held in SNP solutions showed significantly higher relative fresh weight than the control. Vase-life of gerbera flowers was extended by addition of either 50 or 100 mg L⁻¹ carvacrol and either 1 or 2 mg L⁻¹ SNP from 8.3 to 16 d. In addition, the relative fresh weight and solution uptake of gerbera flowers were increased by addition of 100 mg L⁻¹ essential oils and 1 or 2 mg L⁻¹ SNP as compared to that of control flowers. Our results suggest the potential application of essential oils or SNP as novel alternatives to common chemicals used in preservative solutions for gerbera flowers.     

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.     

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.     

Development of SCAR markers and a semi-selective medium for the quantification of strains Ach 1-1 and 1113-5, two Aureobasidium pullulans potential biocontrol agents

Aureobasidium pullulans strains Ach 1-1 and 1113-5 are two effective biocontrol agents against Botrytis cinerea and Penicillium expansum on stored apples. In the present work, a monitoring system allowing their identification and quantification was developed. The methodology used consisted of the development of both molecular markers and a semi-selective medium. The random amplified polymorphic DNA (RAPD) technique was applied to a collection of 15 strains of A. pullulans, including Ach 1-1 and 1113-5. Five specific RAPD fragments were amplified for strain Ach 1-1 and three others for strain 1113-5. Among them, a fragment of 528 bp specific to strain Ach 1-1 (generated with the OPR-13 RAPD primer) and another one of 431 bp specific to strain 1113-5 (amplified with the OPQ-03 RAPD primer) were selected, cloned, sequenced, and used to design sequence-characterized amplified region (SCAR) primers. Three different SCAR markers were amplified: two specific to strain Ach 1-1 (189 bp and 387 bp) and one specific to strain 1113-5 (431 bp). These SCAR primers can clearly identify strains Ach 1-1 and 1113-5 among 14 strains of A. pullulans and among eight yeast strains commonly present on apple fruit surfaces. Their selectivity was also tested using DNA extracted from epiphytic microflora of the apple surface. As a semi-selective medium, PDA medium supplemented with 0.5 mg L⁻¹ euparen, 1 mg L⁻¹ sumico, 2.5 mg L⁻¹ hygromycin B, 30 mg L⁻¹ streptomycin sulphate, and 1 mg L⁻¹ cycloheximide was selected. It inhibited the development of the air microflora and appeared highly toxic for the epiphytic microflora of apple surface without altering the growth of the targeted strains Ach 1-1 and 1113-5. The combination of the semi-selective medium and SCAR markers provides a valuable monitoring tool to specifically identify and quantify A. pullulans strain Ach 1-1 and strain 1113-5 and could be used in future studies to evaluate their population dynamics under various laboratory and practical conditions.     

The efficacy of ultrasonic fumigation for disinfestation of storage facilities against postharvest pathogens

Inoculum of postharvest pathogens can accumulate inside storage rooms and contaminate new batches of fruit and vegetables, but this chain can be broken by disinfecting storage facilities between storage periods. Quaternary ammonium (QA) has been known for over 50 years as an efficient disinfectant against microorganisms, with wide applications in the food industry. The aim of this study was to determine the efficacy of didecyldimethylammonium chloride (Sporekill, designated here as QA^sk), against development of Botrytis cinerea after direct exposure or by ultrasonic fogging. Following direct exposure to a concentration of QA^sk below 5 mg L^?1, a population of 10⁴ conidia of B. cinerea was inactivated after 2 min; ultrasonic fogging with QA^sk at 500 mg L^?1 took 30 min to achieve consistent inactivation. Fumigation at 20 °C was considerably more effective than fumigation at 5 °C, and similar results were obtained for three other postharvest pathogens, Penicillium expansum, Colletotrichum gloeosporioides and Alternaria alternata. These results show that conidia of B. cinerea are highly sensitive to direct exposure to QA^sk, but that effective sanitation of a storage facility by ultrasonic fumigation requires a QA^sk concentration two orders of magnitude greater.     

The combined effects of aqueous chlorine dioxide,fumaric acid,and ultraviolet-C with modified atmosphere packaging enriched in CO2 for inactivating preexisting microorganisms and Escherichia coli O157:H7 and Salmonella typhimurium inoculated on buckwheat sprouts

The combined effects of a sanitizer mixture, ultraviolet-C (UV-C), and modified atmosphere packaging (MAP) on the quality of non-inoculated and inoculated (Escherichia coli O157:H7 and Salmonella typhimurium) buckwheat sprouts were examined. Buckwheat sprouts were treated with a sanitizer mixture (comprising 100 mg L⁻¹ aqueous ClO₂ and 0.3% fumaric acid) and 2 kJ m⁻² UV-C, packaged under two different conditions (air and CO₂ gas) and storage for 8 d at 4 °C. The combination of the sanitizer mixture and UV-C treatment reduced the initial counts of preexisting microorganisms in the buckwheat sprouts by 1.9 log CFU g⁻¹ and reduced the initial inoculated counts of E. coli O157:H7 and S. typhimurium on buckwheat sprouts by 3.0 and 2.3 log CFU g⁻¹, respectively. The preexisting microorganisms and inoculated pathogens in buckwheat sprouts packaged under CO₂ gas were significantly reduced during storage following the combined treatment compared to those of the control by above 95%. Differences in Hunter L^*, a^*, and b^* values among the treatments were negligible. The combined sanitizer mixture and UV-C treatment increased the sprout rutin content by 147%, but there was no significant difference in 2,2-diphenyl-1-picrylhydrazyl radical scavenging activity between treatments during storage. Therefore, the combination of sanitizer mixture made from aqueous ClO₂ and fumaric acid, UV-C irradiation, and MAP can improve the microbial safety and quality of buckwheat sprouts.     

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.     

Controlled atmosphere treatment for control of grape mealybug,Pseudococcus maritimus (Ehrhorn) (Hemiptera: Pseudococcidae), on harvested table grapes

Controlled atmosphere (CA) treatments with ultralow oxygen (ULO) alone and in combinations with 50% carbon dioxide were studied to control grape mealybug, Pseudococcus maritimus (Ehrhorn) on harvested table grapes. Two ultralow oxygen levels, 30 and <0.01 μL L⁻¹, were tested in both ULO and ULO + 50% CO₂ treatments. The ULO treatments with the lower oxygen level were more effective than the ULO treatments at the higher oxygen level. The ULO + 50% CO₂ treatments were more effective than the ULO treatments. Grape mealybug eggs were significantly more tolerant of ULO and ULO + CO₂ treatments than nymphs and adults. A 14 day ULO treatment with 30 μL L⁻¹ O₂ at 2 °C did not achieve 100% mortalities of any life stage. In the presence of 50% CO₂, the 14 d treatment achieved complete mortality of all life stages of the grape mealybug. A 3 d ULO treatment with <0.01 μL L⁻¹ O₂ at 2 °C resulted in 93.3% mortality of nymphs and adults. The 3 d ULO treatment in combination with 50% CO₂ treatments, however, achieved complete control of grape mealybug nymphs and adults and caused 70.5% relative egg mortality. Complete egg mortality was achieved in a 10 d ULO + 50% CO₂ treatment with <0.01 μL L⁻¹ O₂ at 2 °C. Both the 14 d CA treatment with 30 μL L⁻¹ O₂ and 50% CO₂ and the 10 d CA treatment with <0.01 μL L⁻¹ O₂ and 50% CO₂ were tested on table grapes and grape quality was evaluated after two weeks of post-treatment storage. The CA treatments did not have a significant negative impact on grape quality and were safe for table grapes. The study indicated that CA treatments have potential to be developed for postharvest control of grape mealybug on harvested table grapes.     

Effects of ozone treatments on microbial quality and some chemical properties of lettuce,spinach, and parsley

The effects of distilled, ozonated (12 mg L⁻¹) and chlorinated (100 mg L⁻¹) water treatments on inactivation of Escherichia coli and Listeria innocua inoculated on lettuce, spinach, and parsley and on some chemical characteristics (chlorophyll a, chlorophyll b, ascorbic acid, and total phenolic contents and antioxidant activity) of these vegetables were investigated. Chlorine and ozone washes resulted in average log reductions (±standard error) of 2.9 ± 0.1 and 2.0 ± 0.3 for E. coli in the vegetables tested, respectively, while the efficiency of ozone (2.2 ± 0.1 log) was very close to that of chlorine (2.3 ± 0.1 log) on L. innocua. Aqueous ozone did not cause any detrimental effects on the chemical characteristics of the vegetables. The effect of gaseous ozone treatment (950 μL L⁻¹, 20 min) on microbial inactivation and the chemical characteristics of parsley were also determined. This treatment resulted in 1.0–1.5 log reductions in the numbers of both microorganisms but caused significant losses in important bioactive compounds of parsley. Ascorbic acid and total phenolic contents and antioxidant activity in ozone-treated samples were 40.1, 14.4, and 41.0%, respectively, less than the control samples.     

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

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

Effects of cinnamon extract,chitosan coating,hot water treatment and their combinations on crown rot disease and quality of banana fruit

The antifungal activities of cinnamon extract (CE), piper extract (PE) and garlic extract (GE) were evaluated on banana crown rot fungi (Colletotrichum musae, Fusarium spp. and Lasiodiplodia theobromae) in vitro. The assay was conducted with extracts of CE, PE and GE with concentrations of 0, 0.1, 0.5, 1.0, 5.0, 10.0 and 0.75 g L⁻¹ of carbendazim (CBZ) on potato dextrose agar at room temperature. CE completely inhibited conidial germination and mycelial growth of all fungi at 5.0 g L⁻¹. PE totally suppressed mycelial growth of all fungi at 5.0 g L⁻¹ and conidial germination at 10.0 g L⁻¹ except for Fusarium spp. GE had no significant effects but low concentrations (0.1 and 0.5 g L⁻¹) enhanced germ tube elongation of the three fungi. The ED₅₀ values were higher for mycelial growth than for conidia except for Fusarium spp. Combined treatments were investigated on crown rot development in banana fruit (Musa AAA group ‘Kluai Hom thong’). Treatments included 5.0 g L⁻¹ CE, 1% (w/v) chitosan solution, hot water treatment (HWT, 45 °C for 20 min), CE plus chitosan, CE plus HWT and 0.75 g L⁻¹ of CBZ, applied before and after inoculation of the fruit. Crown rot development was assessed during storage at 13 °C for 7 weeks. Disease development was least (25%) on CE treated fruit after inoculation compared to CBZ but was higher when CE was applied before inoculation. Chitosan significantly delayed ripening as in terms of peel color, firmness, soluble solids and disease severity. CE showed no negative effects on quality of fruit. CE plus HWT caused unacceptable peel browning.     

Modified atmosphere packaging preserves quality of SO2-free ‘Superior seedless’ table grapes

‘Superior seedless’ table grapes were stored for 7 days at 0 °C followed by 4 days at 8 °C + 2 days at 20 °C under modified atmosphere packaging (MAP). Two polypropylene films (PP) were used to generate the MAP, the micro-perforated PP-30 and an oriented PP (OPP). The OPP film was applied with and without fungicide (10 μL of trans-2-hexenal or 0.4 g Na₂S₂O₅ kg⁻¹). As control a macro-perforated PP was used. PP-30 packages reached the lowest O₂ and the highest CO₂ levels. Control clusters showed the highest weight losses and decay while almost no losses occurred under MAP treatments. No changes in softness, skin and/or pulp browning, or cluster shatter were found. After shelf life MAP-treated clusters showed slight to moderate stem browning, except under SO₂ where practically no browning occurred while control clusters showed an extreme stem browning. After shelf life, MAP treatments showed good visual appearance and crunchiness, while control fruits were unmarketable. No off-flavors were detected for MAP treatments except for hexenal-treated berries. No remarkable changes for color, firmness, soluble solids content, pH, titratable acidity and maturity index were detected. Total sugars content at harvest was 200 g L⁻¹ and only slight decreases were found after shelf life for most treatments. Total organic acids content at harvest was 15.4 mg 100 mL⁻¹, which remained quite constant after cold storage and shelf life. The main phenolic compounds were flavan-3-ols (over 85% from the total content), hydroxycinnamic acid derivatives and flavonols, whose total amount at harvest was 140 mg kg⁻¹ in a fresh weight basis. After shelf life only slight decreases in total phenolics occurred in all treatments. As a main conclusion, SO₂-free MAP kept the overall quality of clusters close to that at harvest, with few differences when SO₂ was added.     

Treatment with chlorine dioxide extends the vase life of selected cut flowers

The accumulation of bacteria in vase water is often associated with premature senescence in many cut flower species. In the present study, we tested the efficacy of aqueous chlorine dioxide (ClO₂) to extend flower display life by preventing the build-up of bacteria in vase solutions. The addition of 2 or 10 μL L⁻¹ ClO₂ to clean deionized water extended the vase life of Alstroemeria peruviana ‘Senna’, Antirrhinum majus ‘Potomic Pink’, Dianthus caryophyllus ‘Pasha’, Gerbera jamesonii ‘Monarch’, Gypsophila paniculata ‘Crystal’ and ‘Perfecta’, Lilium asiaticum ‘Vermeer’, Matthiola incana ‘Ruby Red’ and Rosa hybrida ‘Charlotte’ flowers by 0.9–13.4 d (7–77%) relative to control (i.e. 0 μL L⁻¹ ClO₂) stems. The beneficial effects of ClO₂ treatment were associated with a reduction in the accumulation of aerobic bacteria in vase water and on cut surfaces of flower stems. ClO₂ treatment was also effective in maintaining or extending the vase life of A. majus ‘Potomic Pink’, Dendrathema × grandiflorum ‘Albatron’, G. paniculata ‘Perfecta’ and M. incana ‘Ruby Red’ flowers even when stems were placed into water containing 10¹¹ CFU L⁻¹ bacteria. The efficacy of 10 μL L⁻¹ ClO₂ in vase water containing 0.2 g L⁻¹ citric acid and 10 g L⁻¹ sucrose to extend the display life of G. jamesonii ‘Lorca’ and ‘Vilassar’ flowers was equal to or greater than other tested biocides (i.e. aluminum sulfate, dichloroisocyanuric acid, 8-hydroxyquinoline sulfate, Physan 20™, sodium hypochlorite). Taken collectively, the results of the present study highlight the potential of aqueous ClO₂ for use as an alternative antibacterial agent in flower vase solutions.     

Effect of antimicrobial compounds on cut Gerbera flowers: Poor relation between stem bending and numbers of bacteria in the vase water

Gerbera flowers (Gerbera jamesonii) often show stem bending. In four cultivars (Tamara, Liesbeth, Cora, and Mickey), we tested the effects on bending of antimicrobial compounds (chlorine bleach, a slow release chlorine compound, 8-hydroxyquinoline citrate [HQC], silver nitrate, carvacrol and thymol), some combined with sugars. At concentrations used for other cut flowers, inclusion in the vase solution of several of the antimicrobial compounds delayed bending, had no effect, or hastened bending. Hastening of bending was found at higher concentrations. It was accompanied with visible damage on the stem ends. Results with HQC indicated high toxicity as it did not delay bending at any of the concentration tested (100–400 mg L⁻¹). At 200 mg L⁻¹ HQC induced growth of bacteria that were not found in the controls. The number of bacteria in the vase water showed a low correlation with bending. Visible toxicity on the stem surface was often associated with a high bacteria count. However, at relatively high concentrations of the antimicrobial compounds stem bending was associated with a low count. This indicated an effect other than bacteria. Water uptake was low in stems that bent early. It is hypothesized that material from dead stem cells resulted in a xylem blockage which led to early bending. Sucrose at 15 g L⁻¹ in combination with an antimicrobial compound (slow release chlorine, HQC) resulted in the absence of stem damage and produced much less bending than the same concentration of the antimicrobial compounds alone. Sucrose apparently counteracted the toxic effects of the antimicrobial chemicals.     

Changes in bread-making quality attributes of bread wheat varieties cultivated in Spain during the 20th century

Genetic gains in quality traits were assessed in grain samples from 4 field experiments involving 16 bread wheat varieties representative of those most widely cultivated in Spain during the 20th century. The allelic composition at three glutenin loci (Glu-A1, Glu-B1, and Glu-D1) was obtained by PCR-based DNA markers and published references. From 1930 to 2000 grain protein content decreased by −0.030% y⁻¹, or in relative terms by −0.21% y⁻¹, but the protein produced per hectare increased by 0.39% y⁻¹. Alveographic tests revealed significant changes in dough rheological properties. Dough strength (W) and tenacity (P) increased at relative rates of 1.38% y⁻¹ and 0.99% y⁻¹, respectively, while dough extensibility (L) decreased by −0.46% y⁻¹, resulting in an increase of 1.45% y⁻¹in dough equilibrium (P/L). The rise in protein quality could be related to the replacement of the null allele by subunits 1 or 2* at Glu-A1 and the prevalence of subunits 7 + 8 and 5 + 10 at Glu-B1 and Glu-D1 loci, respectively, in the most recent varieties. Dough extensibility was affected by water input during the crop cycle, this relationship being partially explained by the presence of the 5 + 10 HMW glutenin subunit. Fermentation tolerance was improved in the most modern varieties. Collapse during fermentation was avoided only in doughs with a W ≥ 159 J × 10⁻⁴ and a P/L ≥ 0.56 mm H₂O mm⁻¹, levels achieved by most of the modern varieties. The over-strong and unbalanced rheological properties of some modern varieties resulted in highly porous doughs, and no clear advances in dough maximum height during fermentation were attained.     

Effects of composite chemical pretreatment on maintaining quality in button mushrooms (Agaricus bisporus) during postharvest storage

This study evaluated the effects of composite chemical pretreatment on the quality of postharvest button mushrooms. Three different treatments, including (T1) control (water), (T2) 1 mmol L⁻¹ Na₂EDTA + 10 mmol L⁻¹ CaCl₂ and (T3) 1 mmol L⁻¹ Na₂EDTA + 2.5% CaCl₂ + 0.5% citric acid + 2.5% sorbitol were used for pretreatments. The results showed that T3-treated samples maintained good firmness and color and had less weight loss during the postharvest storage. Lower levels of H₂O₂, ⁻OH and low malondialdehyde content (MDA) were observed in T3 compared with T1 and T2 samples. Significantly higher soluble protein contents and higher activities in the antioxidant enzymes, i.e., superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX), peroxidase (POD) were observed in T3 compared with T1 and T2 at the end of the storage period (P < 0.05). These results suggest that the T3 treatment could be useful in preserving button mushrooms.