Thiabendazole residue loading in dip,drench and wax coating applications to control green mould and chilling injury on citrus fruit

Green mould (caused by Penicillium digitatum) is a major cause of postharvest losses in citrus. Residue loading of thiabendazole (TBZ) with application methods typically used in South African packhouses and green mould control was studied. TBZ was applied curatively and protectively in dip, drench and wax coating treatments and fruit were inoculated with a TBZ-sensitive or a TBZ-resistant isolate of P. digitatum. The dip treatments consisted of TBZ concentrations of 0–2000 μg mL⁻¹; fruit were dipped for 60 s at 22 °C at a pH of 7. Residues differed between fruit batches and ranged from 0.5 to 1.7 μg g⁻¹ at 1000 μg mL⁻¹ TBZ. Curative dip treatments almost completely controlled green mould (>96% at 1000 μg mL⁻¹ TBZ). The residue level needed for 75% curative control ranged from 0.06 to 0.22 μg g⁻¹, depending on citrus type. Protective treatments were unreliable and control varied from 17% to 97.9% at 1000 μg mL⁻¹ TBZ between fruit batches. Drench treatments consisted of exposure times of 30, 60 and 90 s with 1000 or 2000 μg mL⁻¹ TBZ. Average TBZ residues were 2.14 μg g⁻¹ for Clementine mandarin fruit and 3.50 μg g⁻¹ for navel orange fruit. Green mould control on navel orange fruit resulted in 66–92%, 34–90% and 9–38% control for curative treatments after 6 and 24 h and protective treatments, respectively, depending on fruit batch. Wax with 4000 μg mL⁻¹ TBZ was applied at 0.6, 1.2 and 1.8 L wax ton⁻¹ fruit. Chilling injury was evaluated after fruit storage at −0.5 °C for 40 days. Average TBZ residues loaded was 1.3, 1.3 and 2.7 μg g⁻¹ at the recommended 1.2 L ton⁻¹ for Satsuma mandarin, Clementine mandarin and Valencia orange fruit, respectively. Protective treatments showed lower infection levels (14–20%) than curative treatments (27–40%) for Valencia orange fruit. The same trend was observed with Satsuma (92–95% curative; 87–90% protective) and Clementine mandarin fruit (82–90% curative; 59–88% protective), but control was relatively poor. TBZ application in wax exceeded 5 μg g⁻¹ at higher wax loads (1.2 and 1.8 L ton⁻¹). Wax treatments showed a significant reduction in chilling injury; TBZ had an additive effect. TBZ resistant isolates could not be controlled.     

Imazalil residue loading and green mould control on citrus fruit as affected by formulation,solution pH and exposure time in aqueous dip treatments

Green mould, caused by Penicillium digitatum, is responsible for major postharvest fruit losses on the South African fresh citrus export market. Some of these losses as well as fungicide resistance development can be attributed to sub-optimal imazalil (IMZ) residue loading on citrus fruit (<2 μg g⁻¹), which is commonly the case in South African packhouses. This will result in loss of control and sporulation inhibition on decayed fruit. IMZ formulation [IMZ sulphate and emulsifiable concentrate (EC)], solution pH (IMZ sulphate at 500 μg mL⁻¹ buffered with NaHCO₃ or NaOH to pH 6 and 8) and exposure time (15–540 s) were investigated in order to improve IMZ residue loading and the green mould control on Clementine mandarin, ‘Eureka’ lemon, and navel and Valencia orange fruit. Exposure time had no significant effect on residue loading in the unbuffered IMZ sulphate solution (pH 3). No differences were observed between the pH buffers used, but residue loading improved with increase in pH. The maximum residue limit (MRL) of 5.0 μg g⁻¹ was exceeded following dip treatment in the IMZ EC (after 75 s exposure time), and IMZ sulphate at pH 8 using NaHCO₃ (77 s) or NaOH (89 s) as buffer. The MRL was exceeded after 161 s in IMZ sulphate solutions buffered at pH 6 with either NaHCO₃ or NaOH. An IMZ residue-loading curve was prepared from which residue levels can be predicted for the control of IMZ-sensitive and IMZ-resistant isolates of P. digitatum. From this model the benchmark residue level for 95% control of an IMZ-sensitive isolate and of an IMZ-resistant isolate were predicted to be 0.81 and 2.64 μg g⁻¹, respectively. Residue loading can be improved by adjusting the pH level of an IMZ sulphate solution to 6 or by using the IMZ EC formulation, but exposure time should be restricted to 45 s so as not to exceed the MRL. Conversely, sufficient exposure time of ≈90 s in an unbuffered IMZ sulphate solution (pH 3) will result to improved green mould control, but with residue loading below 2 μg g⁻¹. The resistant isolate could not be controlled adequately with residue levels below the MRL, therewith indicating the practical relevance of IMZ resistance.     

Characterization of postharvest treatments with sodium methylparaben to control citrus green and blue molds

The curative antifungal activity of postharvest sodium methylparaben (SMP) treatments against citrus green (GM) and blue (BM) molds was characterized on different citrus species and cultivars artificially inoculated with Penicillium digitatum or Penicillium italicum and incubated at 20 °C and 90% RH for 7 d or stored at 5 °C and 90% RH for 8 weeks plus 7 d of shelf-life at 20 °C. Effective concentrations were selected in in vivo primary screenings with ‘Valencia’ oranges. SMP at 200 mM was tested at 20, 50 or 62 °C for 30, 60 or 150 s in small-scale trials to determine the best dip treatment conditions. Dips of 200 mM SMP at 20 °C for 60 s were selected and applied alone or in combination with 25 μL L⁻¹ of the conventional fungicide imazalil (SMP + IMZ 25). Imazalil at the very low concentrations of 25 (IMZ 25) or 50 μL L⁻¹ (IMZ 50) were also tested. Effectiveness of SMP alone at 20 °C for 60 s was significantly higher on oranges (cvs. ‘Valencia’ and ‘Lanelate’) than on mandarins (cvs. ‘Clemenules’, ‘Nadorcott’ and ‘Ortanique’), with GM and BM incidence reductions of up to 88% after 7 d at 20 °C. SMP was compatible with IMZ 25 and consistently improved its performance, irrespective of citrus cultivars and storage conditions. All treatments were less effective on ‘Clemenules’ mandarins. On ‘Valencia’ oranges stored for 8 weeks at 5 °C and 7 d at 20 °C, the combined treatment was significantly more effective than the single treatments (reductions of GM and BM incidence of about 50–60% and 90–95%, respectively). In additional tests, 200 mM SMP dips at 20 °C for 60 s did not prevent GM on ‘Valencia’ oranges wounded, treated, inoculated with P. digitatum 24 h later, and incubated at 20 °C for 7 d. In contrast, the treatments IMZ 25 and SMP + IMZ 25 showed significant preventive activity. It can be concluded from these results that SMP aqueous solutions, especially applied at room temperature, might be an interesting nonpolluting control alternative to be included in citrus postharvest disease control programs in the future.     

Sensitivity of Penicillium expansum to diphenylamine and thiabendazole and postharvest control of blue mold with fludioxonil in ‘McIntosh’ apples

Penicillium expansum is one of the most important pathogens that cause blue mold in stored apples. Due to the development of resistance to the postharvest fungicide, thiabendazole (TBZ), an increase in blue mold has been observed in apple storages. The sensitivity of three TBZ-sensitive and three TBZ-resistant isolates of P. expansum to diphenylamine (DPA), scald inhibitor, was tested in vitro. Of the 94 isolates, collected later in the storage season, 41% were found resistant to both DPA and TBZ. To manage the fungicide resistance, a reduced-risk fungicide, fludioxonil, was tested against blue mold caused by TBZ-sensitive and -resistant P. expansum on ‘McIntosh’ apples treated with or without 1000 μg ml⁻¹ of diphenylamine. Fruit were assessed for disease and scald incidence during storage. Diphenylamine controlled scald in treated fruit. Higher disease incidence of blue mold was observed in apples treated with diphenylamine and low concentrations of fludioxonil (3, 5, and 75 μg ml⁻¹). DPA neither positively nor negatively affected the control of blue mold when DPA was applied together with 150, 300 and 600 μg ml⁻¹ of fludioxonil during 12 weeks of storage at 4 °C.     

Can arbuscular mycorrhizal fungi improve competitive ability of dill + common bean intercrops against weeds?

Competition for soil resources plays a key role in the crop yield of intercropping systems. There is a lack of knowledge on the main factors involved in competitive interactions between crops and weeds for nutrients uptake. Hence, the purpose of this work was to compare the effects of arbuscular mycorrhial fungi (Funneliformis mosseae) colonization in interspecific competitive relations and its effect on nutrients uptake and weed control in dill and common bean intercropping. Two field experiments were carried out with factorial arrangements based on randomized complete block design with three replications during 2013–2014. The factors were cropping systems including a) common bean (Phaseolus vulgaris L.) sole cropping (40 plants m⁻²), b) dill (Anethum graveolens L.) sole cropping at different densities (25, 50 and 75 plants m⁻²) and c) the additive intercropping of dill + common bean (25 + 40, 50 + 40 and 75 + 40 plants m⁻²). All these treatments were applied with (+AM) or without (-AM) arbuscular mycorrhiza colonization. In both cropping systems, inoculation with F. mosseae increased the P, K, Fe and Zn concentrations of dill plants by 40, 524, 57 and 1.0 μg kg⁻¹ DW, respectively. Intercropping increased Mn concentration in common bean (4.0 μg kg⁻¹ DW) and dill (3.0 μg kg⁻¹ DW), and also seed yields of both crops (198 g m⁻² and161 g m⁻², respectively). AM colonization improved seed yields of dill and common bean by 169 and 177 g m⁻² in 2013 and 2014, respectively. Moreover, AM application enhanced competitive ability of dill + common bean intercrops against weeds at different intercropping systems. Intercropping significantly changed weed density compared to sole cropping, as weed density was decreased in the dill + common bean intercropping. Diversity (H), Evenness (E) and richness of weed species of weeds for intercrops were higher than those for sole crops.     

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.     

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.     

Effect of treatment with dimethyl dicarbonate on microorganisms and quality of Chinese cabbage

The effects of dimethyl dicarbonate (DMDC) (200 mg L⁻¹) treatment on microorganisms and quality of Chinese cabbage were investigated. The results indicated that in the different tissues treated by DMDC, a significant reduction (P < 0.05) of total aerobic plate count (TAPC) of the leaf (ca. 4.49 log cfu g⁻¹) and stalk (ca. 4.45 log cfu g⁻¹), as well as the count of total yeasts and molds of the leaf (ca. 3.02 log cfu g⁻¹) and stalk (ca. 3.62 log cfu g⁻¹), was obtained in comparison with the control (sterile water dip). However, in the flower bud and/or flower treated by DMDC, the reduction of TAPC (ca. 2.74 log cfu g⁻¹) and counts of total yeasts and molds (ca. 2.26 log cfu g⁻¹) were much lower. DMDC treatment affected appearance and texture early in storage, but an impact on the nutritional composition of Chinese cabbage during storage was not found. Additionally, DMDC treatment significantly (P < 0.05) inhibited the activity of polyphenol oxidase (PPO) and peroxidase (POD) late during storage. Therefore, DMDC is a new and effective alternative for sanitation of Chinese cabbage where a protective measure of appearance quality needs to be adopted.     

Essential oil vapours suppress the development of anthracnose and enhance defence related and antioxidant enzyme activities in avocado fruit

Anthracnose caused by Colletotrichum gloeosporioides is a major postharvest disease in avocados that causes significant losses during transportation and storage. Complete inhibition of the radial mycelia growth of C. gloeosporioides in vitro was observed with citronella or peppermint oils at 8 μL plate⁻¹ and thyme oil at 5 μL plate⁻¹. Thyme oil at 66.7 μL L⁻¹ significantly reduced anthracnose from 100% (untreated control) to 8.3% after 4 days, and to 13.9% after 6 days in artificially wounded and inoculated ‘Fuerte’ and ‘Hass’ fruit with C. gloeosporioides. GC/MS analysis revealed thymol (53.19% RA), menthol (41.62% RA) and citronellal (23.54% RA) as the dominant compounds in thyme, peppermint and citronella oils respectively. The activities of defence enzymes including chitinase, 1, 3-β-glucanase, phenylalanine ammonia-lyase and peroxidase were enhanced by thyme oil (66.7 μL L⁻¹) treatment and the level of total phenolics in thyme oil treated fruit was higher than that in untreated (control) fruit. In addition, the thyme oil (66.7 μL L⁻¹) treatment enhanced the antioxidant enzymes such as superoxide dismutase and catalase. These observations suggest that the effects of thyme oil on anthracnose in the avocado fruit are due to the elicitation of biochemical defence responses in the fruit and inducing the activities of antioxidant enzymes. Thus postharvest thyme oil treatment has positive effects on reducing anthracnose in avocados.     

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.     

Postharvest characteristics of cut dahlia flowers with a focus on ethylene and effectiveness of 6-benzylaminopurine treatments in extending vase life

With the aim of extending vase life of cut dahlia flowers, we investigated the postharvest characteristics of the flowers. Our focus was on the role of ethylene on senescence and on treatments that have extended vase life of other flowers. Continuous exposure to ethylene at 2 or 10 μL L⁻¹ significantly accelerated petal abscission in cut flowers. Flowers continuously immersed in 1 or 10 μL L⁻¹ 2-chloroethylphosphonic acid (CEPA) solution wilted earlier than those treated with distilled water (DW) or 0.15 g L⁻¹ citric acid. Ethylene production from the ovary and ray petal was relatively high (4.5 and 0.9 nL g⁻¹ fresh weight h⁻¹, respectively) at harvest, but decreased gradually over 5 days. No remarkable increase in ethylene production was observed during senescence. Silver thiosulfate complex (STS), an inhibitor of ethylene action, did not extend the vase life of cut flowers, although a high silver concentration was detected in flower organs. In contrast, pulse treatment with 1-methylcyclopropene (1-MCP) and dip treatment with 6-benzylaminopurine (BA) extended the vase life of florets, and BA was more effective than 1-MCP when the flowers were held in both DW and CEPA. BA spray treatment extended vase life of cut ‘Kokucho,’ ‘Kamakura’ and ‘Michan’ flowers. These results suggest that dahlia flower senescence is partially regulated by ethylene, and BA is more effective in delaying the senescence of cut dahlia flowers than ethylene action inhibitors.     

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.     

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.     

Rapid ingress of gaseous 1-MCP and acute suppression of ripening following short-term application to midclimacteric tomato under hypobaria

Our previous studies demonstrated that tomato fruit (breaker or pink) exposed at the midclimacteric stage to hypobaric hypoxia for 6 h exhibited transient increased sensitivity to subsaturating levels of 1-methylcyclopene (1-MCP). In the present study, we examined the effect of gaseous 1-MCP (500 nL L⁻¹, 20.8 μmol m⁻³) applied to mid-climacteric (>60% peak ethylene production) tomato fruit under hypobaric hypoxia (10 kPa, 2.1 kPa O₂,) for 1 h. Application of 500 nL L⁻¹ 1-MCP under atmospheric conditions had little effect on softening and timing and magnitude of peak ethylene production, and moderate effects on respiration and lycopene and PG accumulation. By contrast, midclimacteric fruit exposed to 500 nL L⁻¹ gaseous 1-MCP under hypobaric hypoxia for 1 h showed acute disturbance of ripening. Firmness and hue angle declines were delayed for ten days and peak ethylene production for eleven days compared with trends for the other treatments. Maximum ethylene production did not exceed 50% of maxima for the other treatments and a definitive respiratory climacteric was not observed. Accumulation of internal gaseous 1-MCP was enhanced under hypobaric hypoxia. Internal 1-MCP in fruit exposed to 20 μL L⁻¹ 1-MCP (831 μmol m⁻³) under hypobaric hypoxia for 2 or 10 min averaged 7.5 ± 0.5 and 8.7 ± 1.4 μL L⁻¹, respectively, compared with 0.8 ± 0.3 and 3.9 ± 0.7 μL L⁻¹ in fruit exposed under atmospheric conditions. After 1 h exposure, internal 1-MCP averaged 10.8 ± 2.2 μL L⁻¹ under hypobaric hypoxia compared with 5.3 ± 1.4 μL L⁻¹ under atmospheric conditions. The results indicate that high efficacy of 1-MCP applied under hypobaric hypoxia is due to rapid ingress and accumulation of internal gaseous 1-MCP.     

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.     

Postharvest quality of peeled prickly pear fruit treated with acetic acid and chitosan

White (Opuntia albicarpa) and red (Opuntia ficus-indica) prickly pears were peeled and submerged in chitosan solutions containing different concentrations of acetic acid (1.0 or 2.5%) to obtain ready-to-eat prickly pear products. Some physicochemical (pH, total soluble solids, color, weight loss, and firmness), antioxidant (phenolic compounds and antioxidant activity), microbiological (aerobic mesophile bacteria and yeasts plus molds), and sensory (color, firmness, aroma, flavor, and overall acceptance) characteristics were assessed during 16 d of storage at 4 ± 1 °C and 85 ± 5% of relative humidity. Chitosan coating containing 1.0% of acetic acid delayed weight loss, maintained firmness and color of white prickly pear during the storage time. Most of the sensory values for white prickly pear coated with chitosan containing 1.0 and 2.5% of acetic acid were higher than those obtained for uncoated fruit. Red prickly pear coated with chitosan with 2.5% acetic acid did not maintain its sensory quality throughout 16 d of storage. Chitosan coating with 1 and 2.5% acetic acid did not affect phenolics content and antioxidant activity in white prickly pears; however, an increase of these compounds was observed in red prickly pears. Microbe populations were unchanged in white prickly pears (<10 CFU g⁻¹) and slightly increased in red prickly pears (10–500 CFU g⁻¹) coated with chitosan during the entire storage time.     

Diffusivity of 1-methylcyclopropene in spinach and bok choi leaf tissue,disks of tomato and avocado fruit tissue,and whole tomato fruit

Gaseous 1-methylcyclopropene (1-MCP) has been widely employed for delaying ripening and senescence of harvested fruit and vegetables; however, details on ingress of gaseous1-MCP in plant tissues, which might contribute to differences in responsiveness of different horticultural commodities to 1-MCP, have not been reported. In this study, we used spinach and bok choi leaves, disks from tomato epidermis, stem-scar and avocado-exocarp tissues, and whole tomato fruit to examine ingress of gaseous 1-MCP. Using a dual-flask system, equilibration of 20 μL L⁻¹ (831 μmol m⁻³) 1-MCP through leaf tissue was reached within 1–2 h, and paralleled 1-MCP transfer through glass-fiber filter paper. For disks derived from fruit tissues, changes in 1-MCP concentrations in the dual-flask system showed anomalous patterns, declining as much as 70% in source flasks with negligible accumulation in sink flasks. The pattern of 1-MCP distribution was markedly different from that of ethylene, which approached equal distribution with tomato stem-scar and avocado exocarp but not tomato epidermis tissues. 1-MCP ingress was further addressed by exposing whole tomato fruit to 20 μL L⁻¹ 1-MCP followed by sampling of internal fruit atmosphere. Tomato fruit accumulated internal gaseous 1-MCP rapidly, reaching approximately 8–9 μL L⁻¹ within 3–6 h at 20 °C. Internal 1-MCP concentration ([1-MCP]) declined around 74 and 94% at 1 and 3 h after exposure, respectively. Ingress was similar at all ripening stages and reduced by 45% in fruit coated with commercial wax. Blocking 1-MCP ingress through stem- and blossom-scar tissues reduced accumulation by around 60%, indicating that ingress also occurs through epidermal tissue. Fruit preloaded with 1-MCP and immersed in water for 2 h retained about 45% of post-exposure gaseous [1-MCP], indicating that 1-MCP is not rapidly sorbed or metabolized by whole tomato fruit. Rapid ingress of gaseous 1-MCP was also observed in tomato fruit exposed to aqueous 1-MCP. Both accumulation and post-exposure decline in internal gaseous [1-MCP] are likely to vary among different fruit and vegetables in accordance with inherent sorption-capacity, surface properties (e.g., waxes, stoma), volume and continuity of gas-filled intercellular spaces, and tissue hydration.     

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.     

Internal ethylene concentrations in apple fruit at harvest affect persistence of inhibition of ethylene production after 1-methylcyclopropene treatment

Factors that affect the efficacy of 1-methycyclopropene (1-MCP) treatment of apples [Malus sylvestris (L.) Mill var. domestica (Borkh.) Mansf.] include cultivar and maturity. In this study, ‘McIntosh’, ‘Cortland’ and ‘Empire’ apples were categorized by internal ethylene concentrations (IECs) at harvest, treated with 1 μL L⁻¹ 1-MCP, and the IECs of individual fruit followed at 30 d intervals during air storage at 0.5 °C for 90 d. IECs at harvest ranged from <0.5 μL L⁻¹ to ≥100 μL L⁻¹, 51 < 100 μL L⁻¹, and 10 < 50 μL L⁻¹ for ‘McIntosh’, ‘Cortland’ and ‘Empire’, respectively. 1-MCP treatment resulted in a decrease of IECs in fruit of all cultivars by day 30 after harvest. During subsequent storage IECs remained low in fruit with <1 μL L⁻¹ at harvest, but in ‘McIntosh’, ‘Cortland’ increased in proportion to IECs at harvest, but not in ‘Empire’. The importance of initial IECs in fruit on the persistence of 1-MCP inhibition of ethylene production was confirmed in a further experiment, in which IECs in untreated and 1-MCP treated ‘McIntosh’ and ‘Empire’ apples were measured for up to 194 d. 1-MCP also decreased 1-aminocyclopropene-1-carboxylic acid (ACC) concentrations in fruit. The results of our study are consistent with the hypothesis that IEC modulates the sensitivity of climacteric fruit to 1-MCP.     

Changes in soil quality and plant available water capacity following systems re-design on commercial vegetable farms

Loss of ecological functions due to soil degradation impacts viability of crop production systems world-wide, particularly in vegetable cropping systems commonly located in the most productive areas and characterized by intensive soil cultivation. This paper reports soil degradation caused by intensive vegetable farming, and its reversibility after two to five years of drastic changes in soil management on 16 commercial vegetable farms in south Uruguay. Changes in soil management included addition of green manures and pastures in rotations of vegetable crops, use of animal manure, and erosion control support measures (terracing, reducing slope length, re-orientation of ridges). Soil degradation caused by vegetable farming was assessed by comparing soil properties in 69 vegetable fields with values at reference sites located close to the cropped fields. Effects of the changes in soil management in the 69 fields were assessed by comparing soil properties at the start and to those at the end of the project. Compared to the on-farm reference sites, the vegetable fields contained 36% less SOC, 19% less exchangeable potassium, water stable aggregates with an 18% smaller geometric mean diameter, and 11% lower plant-available soil water capacity. Phosphorus availability was 5 times higher under vegetable cropping compared to the on-farm reference. Phaeozems (Abruptic) revealed greater degradation (44% less soil organic carbon (SOC)) than Vertisols (24% less SOC) and Phaeozems (Pachic) (21% less SOC). After two to five years of improved soil management, SOC concentration in the upper 20 cm increased by on average 1.53 g kg⁻¹ (12%) in the Phaeozems (Abruptic) and 1.42 g kg⁻¹ (9%) in the Phaeozems (Pachic). SOC in Vertisols increased only by 0.87 g kg⁻¹, most likely due to their greater initial SOC concentration. Topsoil carbon sequestration was on average 3.4 Mg ha⁻¹ in the Phaeozems. Multiple linear regression showed the quantity of incorporated amendments, the initial amount of SOC and the clay content to explain 77% of the variability in yearly changes of SOC. Available water capacity increased significantly with SOC particularly due to more water retention at field capacity, resulting in an increase in available water capacity in the first 20 cm of soil of 8.4 mm for every 10 g kg⁻¹ of SOC increase. Results are discussed in relation to perspectives of soil degradation reversal in the long term.