Management of potato dry rot

Dry rot is a postharvest fungal disease affecting potato (Solanum tuberosum L.) tubers. The disease, caused by several species of Fusarium such as F. solani var. coeruleum, F. sambucinum, F. oxysporum, F. avenaceum, F. culmorum, results in significant yield losses. Some Fusarium species associated with the disease produce toxins, which are implicated in mycotoxicoses of humans and animals. The pathogens cannot penetrate the tuber through the lenticels or in the absence of wounds and cause infection only if the potato skin is ruptured. The seed tuber is considered as the main source of inoculum although soil infested by Fusarium spp. also constitutes a source of inoculum. Control of the disease, once provided by the fungicide thiabendazole, is now difficult due to the appearance of thiabendazole-resistant strains and the lack of potato cultivars with high levels of resistance to dry rot. An integrated disease management program including detection strategies, appropriate cultural practices and storage conditions (including a wound healing period) along with the use of synthetic chemical fungicides as seed tuber and/or postharvest treatment is recommended to reduce incidence and severity of dry rot. Recent studies also indicate the possibility that generally recognized as safe (GRAS) compounds and microbial antagonists could eventually be integrated into dry rot management strategies.     

Effect of 1-methylcyclopropene (1-MCP) on reducing postharvest decay in tomatoes (Solanum lycopersicum L.)

1-Methylcyclopropene (1-MCP as SmartFresh™ technology), an ethylene antagonist, was evaluated for affecting postharvest decay caused by Alternaria alternata, Botrytis cinerea, and Fusarium spp. on ‘Quality 23’ and ‘Seminis 35’ tomatoes at green or pink stages. Fruit with natural or artificial infection were subjected to 1-MCP at 0.0 μL L⁻¹, 0.6 μL L⁻¹ for 12 h, and 1.0 μL L⁻¹ for 6 h. After 31-42 d storage, disease incidence and severity of individual diseases in 1-MCP treated fruit was significantly reduced compared with that of the untreated controls, except in one inoculated test for ‘Quality 23’ where severity of Alternaria rot in 1.0 μL L⁻¹ treated fruit were significantly higher than that of the untreated control. Fruit treated with 1-MCP at 1.0 L⁻¹ for 6 h also had significantly higher incidence of Alternaria rot in the inoculated ‘Quality 23’ and in the non-inoculated ‘Seminis 35’ compared with the fruit treated with 1-MCP at 0.6 μL L⁻¹ for 12 h. The results of this study indicate that 1-MCP can reduce postharvest decay within a certain storage period.     

Pheophytinase activity and gene expression of chlorophyll-degrading enzymes relating to UV-B treatment in postharvest broccoli (Brassica oleracea L. Italica Group) florets

Pheophytinase (PPH) activity and gene expression of chlorophyll (Chl)-degrading enzymes relating to UV-B treatment in postharvest broccoli (Brassica oleracea L. Italica Group) florets were determined. PPH is involved in the dephytylation of Mg-free Chl a, pheophytin (Phy) a. However, in vitro chlorophyllase (Chlase, EC.3.1.1.14) also uses Phy a as a substrate to produce pheophorbide (Pheide) a by dephytylation. For an accurate determination of PPH activity, the PPH protein fraction was separated from Chlase protein by ammonium sulfate precipitation. The protein precipitated by 45-60% saturated ammonium sulfate included a little bit of Chlase activity and was suitable for PPH determination. PPH activity in broccoli florets treated with a UV-B dose of 19 kJ m⁻² was repressed for the first 2 d of storage at 15 °C, whereas it increased gradually with senescence of control broccoli florets. The expression level of BoCLH1 was reduced in broccoli florets on day 4 of storage, while BoCLH2 and BoCLH3 were up-regulated with UV-B treatment. A high BoPAO expression level was found in senescent broccoli florets, and the up-regulation of this gene was delayed by UV-B treatment. The highest expression level of BoPPH was found in the control, and its expression was clearly repressed by UV-B treatment on day 2 of storage. We suggest that the up-regulation of Chl-degrading enzyme genes could be delayed by UV-B treatment, resulting in the suppression of floret yellowing in stored broccoli.     

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.     

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

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

The combination of curing with either chitosan or Bacillus subtilis CPA-8 to control brown rot infections caused by Monilinia fructicola

Recently, it has been reported that brown rot in peaches and nectarines can be effectively controlled by exposing fruit to 50 °C for 2 h and 95-99% relative humidity (RH). This treatment was effective at reducing infections that had become established in the field. However, it did not provide protection for further Monilinia fructicola infections, indicating that fruit was susceptible to subsequent infections after the treatment process and before cool storage. Chitosan and Bacillus subtilis (strain CPA-8) were evaluated for their ability to prevent M. fructicola infections and for their ability to complement the heat treatment. Two chitosan concentrations (0.5% or 1%) were applied at three temperatures (20, 40 or 50 °C) for 1 min to wounded and unwounded fruit that were artificially inoculated with M. fructicola. One percent chitosan applied at 20 °C had a preventive effect against further M. fructicola infections on heat-treated fruit that had been previously inoculated: brown rot incidence was reduced to 10%, in comparison with the control (73%). However, chitosan applied to wounded fruit had a poor preventive effect. The antagonist, B. subtilis CPA-8, had a preventive effect in controlling M. fructicola infections: the incidence of brown rot was reduced to less than 15% for both varieties evaluated (‘Baby Gold 9’ and ‘Andros’ peaches), in comparison with the control fruit (higher than 98%). In contrast, when fruit were stored at 0 °C, this preventive effect was not detected. These findings indicate that heat-treated fruit can be protected from subsequent fruit infection after heat treatment by use of chitosan or B. subtillis CPA-8, thereby providing packinghouses with an effective biologically based, combined approach to the management of postharvest brown rot.     

Control of lemon postharvest diseases by low-toxicity salts combined with hydrogen peroxide and heat

The effectiveness of potassium sorbate, sodium bicarbonate and potassium phosphite combined with heat and hydrogen peroxide in the presence of CuSO₄ to control major lemon postharvest diseases was investigated on artificially infected fruit. Green and blue molds, which both require wounds for infections to occur, were controlled by combination of hydrogen peroxide followed by inorganic salts, even when the temperature solutions were 25 °C. Control of sour rot was poor with salt solutions alone but significantly improved in treatments including hydrogen peroxide followed by potassium sorbate or sodium bicarbonate at 50 °C. Phomopsis stem-end rot was effectively controlled by potassium sorbate and potassium phosphite at 20 °C, and diplodia stem-end rot was partially controlled only by potassium sorbate. Applications of either potassium sorbate or a sequence of hydrogen peroxide followed by potassium phosphite were the most promising treatments, primarily because they controlled most of the diseases without the need to heat the solutions. These treatments controlled postharvest citrus diseases to useful levels and could be suitable alternative to conventional fungicides, or could be applied with them to improve their performance or to manage fungicide resistant isolates.     

Ethanol vapor and saprophytic yeast treatments reduce decay and maintain quality of intact and fresh-cut sweet cherries

The objective of this study was to evaluate the use of an ethanol vapor release pad and a saprophytic yeast Cryptococcus infirmo-miniatum (CIM) to reduce decay and maintain postharvest quality of intact or fresh-cut sweet cherries (Prunus avium) cv. Lapins and Bing. Intact or fresh-cut fruit were packed in perforated clamshells (capacity 454 g) and stored at 1, 10 or 20 °C for up to 21, 14 and 8 d, respectively. For ethanol treatment, a pad made with silica gel powder containing 10 g ethanol and covered with perforated film, which allows ethanol vapor to diffuse gradually, was attached to the upper lid of the clamshells. Ethanol treatment caused accumulation of ethanol in the packaging headspace, about 10 μL L⁻¹ with little change within 14 d at 1 °C, 23 μL L⁻¹ at d 1 and decreased to 15 μL L⁻¹ at d 10 at 10 °C, and 26 μL L⁻¹ at d 1 and decreased to 13 μL L⁻¹ at d 3 at 20 °C. Ethanol content in fruit was less than 9 mg kg⁻¹ in all the control fruit, and increased to 16, 34 and 43 mg kg⁻¹ in ethanol-treated fruit at 1, 10 and 20 °C, respectively. Nonetheless, a sensory taste panel did not perceive any flavor difference from the ethanol treatment. The ethanol treatment retarded softening, darkening, and acid decrease in fruit as well as discoloration of the stems, and extended shelf-life of intact cherries. Ethanol reduced brown rot (Monilinia fructicola) in fresh-cut cherries stored at 20 °C, but not at 1 and 10 °C. A pre-packaging dip in CIM completely controlled brown rot in inoculated fresh-cut cherries stored at 1 °C, and in naturally infected cherries at 20 °C.     

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

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

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.     

Control of lemon green mold by a sequential oxidative treatment and sodium bicarbonate

A sequential oxidative treatment (SOT), using sodium hypochlorite (NaClO) and hydrogen peroxide (H₂O₂) in the presence of a cupric salt inhibited in vitro growth and germination of Penicillium digitatum conidia, causal agent of citrus green mold. Here, modifications of this SOT were evaluated in vivo to control this disease in inoculated lemons. The treatment that consisted of two sequential 2-min baths: one with 200 mg L⁻¹ NaClO followed by a second with 600 mmol L⁻¹ H₂O₂ in the presence of 6 mmol L⁻¹ CuSO₄, resulted in 50% of disease control. When this treatment was combined with a third 2-min bath containing 30 g L⁻¹ NaHCO₃ at 37 °C (SOT-NaHCO₃) and applied at 24 h post-inoculation, green mold incidence was reduced to ∼5%. In non-inoculated lemons stored at 5 °C for 45 d, this treatment did not modify the appearance or weight compared to untreated lemons. Furthermore, phenolic content and the oxygen consumption rate in flavedo and albedo tissues were not affected by the SOT-NaHCO₃. The malondialdehyde content in flavedo tissues increased immediately after treatment, but decreased to levels similar to control fruit 2 d later. The SOT-NaHCO₃ combines compounds that are safe to the environment and human health, thus it represent a potential alternative to synthetic fungicides for the integrated control of postharvest diseases.     

Defense responses of tomato fruit to exogenous nitric oxide during postharvest storage

Nitric oxide (NO), an important signalling molecule, has shown diverse physiological functions in plants. We investigated physiological responses of harvested tomato fruit (Solanum lycopersicum cv. Ailsa Craig, AC) to NO treatment. NO released by 1 mM sodium nitroprusside (SNP) aqueous solution could effectively retard pericarp reddening of tomato fruit, suppress ethylene production, and influence quality parameters during storage. The activity of antioxidant enzymes in NO-treated tomato fruit was higher in the late storage period compared to the control. RT-PCR analysis showed that expression of six genes related to fruit ripening was regulated by NO treatment, resulting in an increase in resistance of tomato fruit to gray mold rot caused by Botrytis cinerea. Our results demonstrated that application of NO could be a potential method for treating harvested fruit in order to delay ripening, maintain quality and enhance resistance of fruit to fungal pathogens.     

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

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

Blue light alters infection by Penicillium digitatum in tangerines

The effect of blue light exposure on Penicillium digitatum infection of tangerines during postharvest storage was investigated. In citrus, P. digitatum is one of the most important fungi causing diseases that result in postharvest loss. There is increasing interest in development of environmentally sustainable and consumer-friendly strategies of decay control. Strategies based on a plant's immunity can minimize pathogen infection of fruit. Light signalling affects plant-pathogen interactions and blue light may modulate phospholipase activation, a key step in plant immune responses. Exposure of fruit to 410-540 nm blue light at a fluency of 40 μmol m⁻² s⁻¹ reduced infection by P. digitatum and induced phospholipase A₂ (PLA₂) gene expression. Inhibition of PLA₂ activity allowed infection, whereas inhibition of phospholipase D (PLD) expression by 580-670 nm red light at the same fluency was correlated with infection. These data strongly suggest that induction of lipid signalling by light reduces fungal colonization by P. digitatum in citrus fruit.     

Imazalil residue loading and green mould control in citrus packhouses

Imazalil (IMZ) is commonly applied in South African citrus packhouses for the control of green mould, caused by Penicillium digitatum, yet the disease still causes significant postharvest losses. The maximum residue limit (MRL) for IMZ on citrus fruit is 5 μg g⁻¹, whereas 2-3 μg g⁻¹ is a biologically effective residue level that should at least inhibit green mould sporulation. Standard compliance auditing of residue levels of citrus fruit, however, indicate that fruit from the majority of packhouses have residues of ≈1 μg g⁻¹. Poor disease control from insufficient residue loading might further be compounded by the presence of IMZ-resistant isolates of P. digitatum in packhouses. This study was conducted to assess the current status of IMZ application in South African packhouses, to determine the adequate residue levels needed to control green mould and inhibit its sporulation using both IMZ sensitive and resistant isolates, to investigate IMZ application methods and resultant residue levels in commercial citrus packhouses, and to study optimisation of modes of IMZ application in citrus packhouses. Factors studied were IMZ concentration, application type (spray vs. dip and drench), exposure time, solution temperature and pH, as well as curative and protective control of P. digitatum. The packhouse survey showed that the majority of packhouses applied IMZ in a sulphate salt formulation through a fungicide dip tank, and loaded an IMZ residue of ≈1 μg g⁻¹. In dip applications, IMZ had excellent curative and protective activity against Penicillium isolates sensitive to IMZ. However, curative control of IMZ resistant isolates was substantially reduced and protective control was lost, even at twice the recommended concentration, nor was sporulation inhibited. The use of sodium bicarbonate (2%) buffered imazalil sulphate solutions at pH ±8, compared with pH ±3 of the unbuffered solutions, markedly increased IMZ residue loading on Navel and Valencia oranges and improved curative and protective control of IMZ resistant isolates. Exposure time did not affect IMZ residue loading in IMZ sulphate solutions at pH 3, although the MRL was exceeded after 45 s exposure in pH 8 solutions. Imazalil applied through spray or drench application improved residue loading, but green mould control was less effective than after dip application.     

Postharvest salicylic acid treatment reduces storage rots in water-stressed but not unstressed sugarbeet roots

Exogenous application of salicylic acid (SA) reduces storage rots in a number of postharvest crops. SA's ability to protect sugarbeet (Beta vulgaris L.) taproots from common storage rot pathogens, however, is unknown. To determine the potential of SA to reduce storage losses caused by three common causal organisms of sugarbeet storage rot, freshly harvested roots were treated with 0.01, 0.1, 1.0 or 10 mM SA, inoculated with Botrytis cinerea, Penicillium claviforme, or Phoma betae, and evaluated for the severity of rot symptoms after incubation at 20 °C and 90% relative humidity. Roots were obtained from plants that received sufficient water or were water-stressed prior to harvest. Roots from water-stressed plants were included since water-stress increases sugarbeet root susceptibility to storage rot and SA mitigates drought effects in other plant species. SA at concentrations of 0.01–10 mM had no effect on the severity of storage rot caused by B. cinerea, P. claviforme, or P. betae in roots from plants that received sufficient water prior to harvest. However, SA at these same concentrations reduced the severity of rot symptoms for all three pathogens in roots from plants that were water stressed before harvest. For water-stressed roots, all concentrations of SA produced statistically equivalent reductions in the weight of rotted tissue for each pathogen, and on average, SA reduced rot severity due to B. cinerea, P. claviforme, and P. betae by 54, 45, and 58%, respectively. SA reduced rot from all three pathogens by reducing lesion size, but did not affect the incidence of infection. The ability of SA to reduce rot severity in water-stressed roots, but not in roots that received sufficient water before harvest suggests that SA alleviated the negative impact of water stress but did not directly protect sugarbeet roots against storage rots.     

UV-C irradiation induces defence responses and improves vase-life of cut gerbera flowers

UV-C (λ = 254 nm) irradiation was effective in reducing Botrytis cinerea floret specking (i.e., lesion development) and maintaining a better postharvest quality of cut gerbera flowers. A range of UV-C doses (0.5-10.0 kJ m⁻²) was tested on ‘Ice cream’ and ‘Ecco’ gerbera flowers to activate germicidal and inducible defence mechanisms. Irradiation of B. cinerea cultures with 0.5, 1.0, 2.5 and 5.0 kJ m⁻² UV-C resulted in up to a 10-fold reduction of conidial germination percentages and significant (P < 0.05) delay of mycelium growth, compared to the non-irradiated control cultures. Moreover, lesion diameters on gerbera florets inoculated with UV-C irradiated B. cinerea cultures were reduced by up to 70%, suggesting that UV-C had a negative effect on the pathogenic strength of the fungi. Lesion diameters on florets of UV-C irradiated gerberas were reduced by up to 55% giving evidence that defence responses in the host tissue were induced. Concentration of total phenolics seemed to be unaffected by 0.5 kJ m⁻² UV-C treatment in both cultivars, but polyphenol oxidase (PPO) activity increased and remained higher compared to the non-irradiated control flowers throughout the 48 h storage period at 20 °C. The increase of PPO suggests that this enzyme might play an important role in host defence mechanisms that suppressed B. cinerea floret specking. Gerbera flowers irradiated with 1.0 or 10.0 kJ m⁻² UV-C showed improvement in vase-life by 1.8 and 2.4 d, decrease in stem break percentages by 43 and 29% and delay in stem break incidence by 3.3 and 1.3 d, respectively.     

Hot water treatments reduce leaf yellowing and extend vase life of Asiatic hybrid lilies

The vase life of Asiatic lilies can be limited by leaf yellowing, which can be caused by exposure to low light or temperature during winter growth or in storage. We examined the use of postharvest hot water treatments (HWTs) as a means of reducing leaf senescence in stored (4 °C for 2 weeks) and non-stored Asiatic hybrid lily ‘Elite’ (Lilium sp.). A range of HWTs (45-55 °C for 2.5 or 5 min) was applied to leaves on cut lily stems (but not flowers). Higher temperatures and the longer duration resulted in heat damage, but treatments of 50 °C for 5 min and 52.5 °C for 2.5 min were found to be optimal for minimising leaf yellowing with trace levels of heat damage for both non-stored and stored stems. The onset of yellowing was delayed by 3-4 d, and the occurrence of an unacceptable level of yellowing eliminated for up to 12 d (compared with <6 d for control stems). The physiological effects of these optimal HWTs were examined in terms of water uptake, chlorophyll fluorescence and chlorophyll degradation. Water uptake for optimal HWTs during shelf life was reduced by more than 50% of the control stems. Chlorophyll fluorescence of leaves on control stems showed a reduction in yield (F_v/F_o) over time, which was more marked in lower than upper leaves (thus correlating with yellowing, which was more severe in the lower leaves). Although both optimal HWTs resulted in an initial reduction in yield, there was a recovery over time resulting in a yield that, by 12 d, was as high or significantly higher than control leaves (particularly for the lower leaves). All treatments showed a reduction in chlorophyll content (total, chlorophyll a and chlorophyll b), but control leaves had significantly lower levels after 7 d. HWTs show potential as a non-chemical, simple means of delaying leaf yellowing of Asiatic lilies and thus increasing vase life.     

Structural and physiological changes associated with the skin spot disorder in apple

Skin spot is an important physiological disorder of ‘Elstar’ apples (Malus × domestica Borkh.) that occurs after fruit have been removed from controlled atmosphere storage. Skin spots are irregular patches of small, round, brown blemishes. Cross-sections reveal a browning of protoplasts (coagulated) and of cell walls that extends into the hypodermis. Skin spots are always associated with linear, gaping and non-gaping microcracks in the cuticle. Staining of apple skin with calcofluor white usually results in white fluorescence of cell walls but, within a skin spot, the white fluorescence is weak or absent. Cell walls within, and in the immediate vicinity of skin spots stain with phloroglucin/HCl indicating the presence of lignin. The area of skin affected by skin spots was positively and linearly correlated with the area of the non-blush fruit surface infiltrated by acridine orange. In general, skin spots were limited to the non-blush fruit surface and occurred more frequently near the stem-end than the calyx region of the fruit. Skin spot areas were correlated with a 2.5-fold increase in water vapour permeability compared with unaffected areas (23.8 ± 4.0 m s⁻¹ with skin spots, 9.6 ± 2.1 × 10⁻⁵ m s⁻¹ without skin spots). Strips of the fruit skin from regions with skin spots had an increased maximum force and modulus of elasticity. Dipping fruit in ascorbic acid (0.1 or 0.3 mM for 10 min) before storage decreased the area affected by skin spots. There was no effect of dipping in ethanol/water (70%, v/v, 15 min) or in solutions of captan (1.5 g L⁻¹, 10 min) or trifloxystrobin (0.1 g L⁻¹, 10 min). In contrast, prestorage treatment with 1-methylcyclopropene (630 nL L⁻¹ for 24 h) or poststorage incubation in H₂O₂ (10% for 2, 6, 10 and 16 h) increased skin spots. Our data are consistent with a typical cell response to an oxidative burst that seems to be focussed on particular regions of the ‘Elstar’ fruit surface by concentrations of cuticular microcracks, and that is possibly caused by reoxygenation injury upon removal from CA storage.     

Integrated control of citrus green and blue mold and sour rot by Bacillus amyloliquefaciens in combination with tea saponin

A strain of Bacillus amyloliquefaciens HF-01, isolated from citrus fruit surfaces, was screened for in vitro antagonism toward Penicillium digitatum and identified, based on Biolog identification and phylogenetic analysis of 16S rDNA sequences. The isolate was further evaluated alone, or in combination with tea saponin (TS) on artificially inoculated ‘Wuzishatangju’ mandarin fruit. The results showed that the isolate performed significantly better than the water control in reducing the incidence of green and blue mold and sour rot, but was not as effective as the fungicide treatment. Biocontrol activity of B. amyloliquefaciens HF-01 was significantly improved by addition of TS, which might influence the formation of a bacterial biofilm and stimulate the antagonist population in wounds. The treatment comprising HF-01 combined with 50 μg mL^?1 TS was as effective as the fungicide treatment, which gave more than 90% control of green and blue mold and sour rot. B. amyloliquefaciens HF-01 alone or in combination with a low dosage of TS significantly reduced postharvest decay without impairing any of the other fruit quality parameters. The combination of B. amyloliquefaciens HF-01 and TS could be an alternative to synthetic fungicides for the control of citrus postharvest diseases.