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.     

Effects of ethylene on volatile emission and fragrance in cut roses: The relationship between fragrance and vase life

The relationship between fragrance and vase life and the role of ethylene on volatile emission in cut rose flowers was investigated. No relationship was observed between the amounts of volatile compounds emitted and vase life when fragrant and non-fragrant rose cultivars were compared. Neither ethylene production nor respiration rate of flowers was directly related with vase life. Volatile production during vase life was differential and independent among volatiles originating from different biosynthetic groups. Ethylene did not play a role in the regulation of volatile emission in rose flowers. Endogenous ethylene production was very low in most of the cultivars and did not show autocatalytic production trends. Volatile emission patterns during vase life did not parallel endogenous ethylene production. Exogenous ethylene exposure had differential effects among all cultivars, regardless of the fragrance of the flower. Fragrant cultivar ‘Osiana’ was highly sensitive to exogenous ethylene, with petals abscising within 24 h of ethylene (1 μL L^?1) exposure while other fragrant cultivars ‘Erin’ and ‘Lovely Dream’ had low ethylene sensitivity. Volatile production was unaffected by exogenous ethylene. The results of this study indicate that volatile emission in cut roses is not regulated by endogenous or exogenous ethylene and occurs independently of petal senescence and/or abscission. These results provide a better understanding of the complexity of volatile emission in rose flowers.     

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.     

A neural network technique to develop a vase life prediction model of cut roses

We developed neural network (NN) models using environmental, morphological, and physiological parameters to predict the vase life of cut roses grown in a greenhouse. These parameters were obtained during the growing and pre-marketing stages. A back-propagation training algorithm was used to develop the vase life prediction model. The network consisted of 29, 26, and 1 processing units in the input, hidden, and output layers, respectively. The NN was trained using the data of 123 cut ‘Asami Red’ roses and was validated using other data obtained from 30 cut roses. The results showed that the NN model had a relatively higher predictability (r² = 0.886, RMSEP = 0.984) between the predicted and observed values. Mixed data of rose cultivars ‘Asami Red’, ‘Bridal Pink’ and ‘Sonia’ were used to train the model. The validated model using the test data of the three cultivars still showed a good predictability (r² = 0.835, RMSEP = 1.126). The analyses showed that the NN model can predict the vase life of cut roses better than traditional statistical methods. Thus, we conclude that the NN is a superior approach to predict and guarantee the vase life of cut roses.     

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 symptoms of senescence and chilling injury on inflorescences of Heliconia bihai (L.) cv. Lobster Claw and cv. Halloween

Inadequate temperatures during the shipping and commercialization of cut tropical flowers may accelerate the senescence process and cause chilling injury, leading to symptoms that have not yet been described for Heliconia bihai. The aim of the present study was to evaluate physiological responses in cut inflorescences of H. bihai cv. Lobster Claw (LC) and cv. Halloween (HW) as well as symptoms of senescence and chilling injury. For such, changes in fresh weight, bract color (L*, a* and b*), percentage of absolute integrity (PAI) of cell membranes and leakage of potassium ions (LPI) were determined. The flowering stems were evaluated at five different intervals after harvest (0, 2, 4, 6 and 8 d). A refrigerated treatment (RT) with a temperature of 6.5 °C and 85% relative humidity was compared to a control treatment (CT) at room temperature of 24 °C and 66% relative humidity. Both cultivars stored at 6.5 °C exhibited dryness of bract tissue (symptom of senescence) and dark stains that became brownish and evolved to necrosis (symptom of chilling injury). The visual quality of inflorescences decreased with time in both cultivars maintained without refrigeration. The severity of chilling injury increased with the length of storage time in both cultivars. There was a significant reduction in the fresh weight of inflorescences in both treatments (RT and CT) and both cultivars (LC and HW). Bract color changed in both cultivars at 6.5 °C. There was no change in PAI throughout the evaluation period in the inflorescences stored at room temperature, whereas those stored at 6.5 °C for 6 and 8 d had lower PAI values. The inflorescences in the control treatment underwent no change in LPI values, whereas those stored under refrigeration had increased LPI values after the sixth day of storage. The physiological responses of cut Heliconia flowers were influenced by storage period and temperature, as demonstrated by visual symptoms of chilling injury and senescence.     

1-MCP pretreatment prevents bud and flower abscission in Dendrobium orchids

Dendrobium orchid inflorescences were treated for 4 h at 25 °C with or without 100–500 nl/l 1-MCP and were then placed in water at 25 °C to follow abscission. In controls, depending on the experiment, 20–80% of the floral buds and 0–20% of the open flowers abscised within 1 week. The 1-MCP pretreatment largely prevented this abscission. If flowers were exposed to 1.0 μl/l ethylene for 3 days, all floral buds and all open flowers abscised within the 3 days of treatment. 1-MCP treatment just prior to ethylene treatment largely prevented the ethylene effect. Treatment with STS was as effective as treatment with 1-MCP. Dendrobium inflorescences are usually shipped by air in cardboard boxes lined with plastic film. The stem ends are placed in plastic tubes filled with water. After shipment and placement in water, a considerable percentage of the buds, and some flowers, abscise. This is probably due to elevated ethylene concentrations inside the boxes. Treatment of the inflorescences with 100–500 nl/l 1-MCP prior to simulated air transport largely prevented abscission during vase life. 1-MCP treatment inhibited ethylene production of the inflorescences by lowering both ACC synthase in open flowers and ACC oxidase activity in floral buds.     

Opening of cut Iris x hollandica flowers as affected by temperature,dry storage,and light

Flower opening in Iris (Iris x hollandica) depends on elongation of the pedicel + ovary. This elongation lifts the bud above the point where the sheath leaves no longer mechanically inhibit lateral tepal movement. We here report on the effects on flower opening of storage at various temperatures, of holding the flowers dry rather than in water, and of a 12 h light/dark cycle instead of darkness, in cv. Blue Magic. During 3 d of storage in darkness at 11 °C or 6 °C the flowers placed in water opened. Flowers stored at 3.0 °C did not open during the storage period but did so during subsequent vase life at 20 °C. Flowers stored in water at 0.5 °C remained closed, even during subsequent vase life at 20 °C. None of the flowers that were stored dry for 3 d at 15 °C, 11 °C, 6 °C, 3 °C or 0.5 °C opened during vase life. Compared to flowers placed in continuous darkness, a rhythm of 12 h light and 12 h darkness inhibited opening during a 3 d storage period at 20 °C. It is concluded that cut Iris flowers (a) can be stored in water at 3 °C for more than a week, but cannot be stored for 3 d or more in water at 15 °C, 11 °C, 6 °C or 0.5 °C, and (b) cannot be stored dry for long (under the present conditions 3 d or longer) at any of these temperatures. Iris flowers were found to be chilling-sensitive, although only at temperatures of about 0.5 °C.     

Postharvest UV-C irradiation on cut Freesia hybrida L. inflorescences suppresses petal specking caused by Botrytis cinerea

Postharvest petal specking caused by Botrytis cinerea is a major concern for freesia growers and sellers in Holland and the UK. Germicidal and inducible host defence effects of UV-C irradiation were evaluated. UV-C irradiation of freesia inflorescences after artificial inoculation with B. cinerea (i.e. the germicidal effect) was more effective in reducing petal specking, compared to UV-C treatment before artificial inoculation (i.e. the defence induction effect). Cut freesia inflorescences exposed to 1 kJ m^?2 UV-C after artificial inoculation with 10⁴ B. cinerea conidia mL^?1 displayed reduced disease severity scores, lesion numbers and lesion diameters by 74, 68 and 14%, respectively, compared to non-irradiated control inflorescences. In contrast, UV-C irradiation with 1 kJ m^?2 before artificial inoculation reduced lesion numbers and lesion diameters by 13 and 24%, compared to the non-irradiated controls. Higher UV-C doses of 2.5 or 5 kJ m^?2 reduced disease severity scores, lesion numbers and lesion diameters when applied after artificial inoculation, but enhanced disease when applied before artificial inoculation. Vase life of cut freesia inflorescences irradiated with 0.5, 1 or 2.5 kJ m^?2 UV-C was maintained equal to non-irradiated controls. However, 5 kJ m^?2 resulted in phytotoxicity evident as petal discoloration and reduced vase life compared to non-irradiated inflorescences.     

Increase in DNA fragmentation and the role of ethylene and reactive oxygen species in petal senescence of Osmanthus fragrans

In sweet osmanthus (Osmanthus fragrans Lour.) flowers, petal browning, partial abscission and wilting are the visible symptoms of senescence, 4–5 days after flowering, which seriously affect its ornamental and economic value. In the present study, DNA fragmentation was used as a marker to investigate the role of ethylene and reactive oxygen species (ROS) in flower senescence of O. fragrans ‘Liuye Jingui’. In intact plants, nuclear shrinkage and DNA fragmentation occurred at the late full flowering stage when senescence symptoms became visible. This coincided with a rapid increase in ethylene production, ROS generation and lipid peroxidation. To further determine the role of ethylene and ROS in flower senescence, cut flowers were treated with ethephon, silver thiosulphate (STS), hydrogen peroxide (H₂O₂), and vitamin C (Vc). The vase life of cut flowers was significantly prolonged by 0.2 mM STS and 2.5 mM Vc treatments, but reduced by 0.03% H₂O₂ and 500 mg L⁻¹ ethephon treatments, compared to distilled water. The percentage of DNA fragmentation was dramatically increased by ethephon but reduced by STS treatment throughout vase life. In contrast, the dramatic increase of DNA fragmentation in the H₂O₂ treated samples was only observed at day three, and clear petal abscission and rapid petal wilting occurred only with ethephon. Compared with the distinguishable nuclei and complete vacuoles in both STS treatment and distilled water, ethephon treatment caused substantial damage to large central vacuoles and other organelles, and many petal cells twisted out of shape due to a loss of cytoplasm, resulting in rapid petal wilting. Thus, it is concluded that ethylene plays an important role in flower senescence of sweet osmanthus, enhancing DNA fragmentation, damaging cellular structure, and leading to petal abscission and wilting. In addition, ROS is also involved in the regulation of late DNA degradation and lipid peroxidation.     

The effects of 1-MCP in cyclodextrin-based nanosponges to improve the vase life of Dianthus caryophyllus cut flowers

The present research investigated the effects of a non-volatile formulation of 1-methylcyclopropene (1-MCP) embedded in different cyclodextrin (CD)-based nanosponges (NSs) to extend the postharvest longevity of an ethylene-sensitive carnation cultivar. Cut flowers of Dianthus caryophyllus L. ‘Idra di Muraglia’ were treated with α- and β-CD-based nanosponge-1-MCP complexes (α- and β-NS complexes) in tap water to achieve two different concentrations of active ingredient (0.25 and 0.5 μL L^?1). Treated flowers were compared to cut stems exposed to equivalent concentrations of volatile 1-MCP as well as a tap water control with or without pure α- and β-NS. Identical nanoporous compounds were applied by perfusion to yield a total of 15 treatments. Twenty-four hours after the treatments were applied, the cut flowers were exposed to exogenous ethylene (1 ± 0.2 μL L^?1) for 24 h. The postharvest carnation flower and leaf quality in addition to ethylene production levels were determined daily (beginning 24 h after treatment). None of the α-NS complex applications statistically improved the vase life of cut flowers; however, β-NS complexes were effective in preventing senescence, reducing ethylene production (measured at nearly nil after 11 d), and maintaining original petal color longer. These results were particularly strong at the lowest concentration (0.25 μL L^?1) of β-NS complex. Overall, this method promoted cut flower longevity (loss of ornamental value after 14.7 d; complete damage at day 18.5) better than the commercial 1-MCP gaseous application method.     

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 respiration of fresh-cut butterhead lettuce under controlled atmospheres using low and superatmospheric oxygen conditions with different carbon dioxide levels

The effect of different O₂ levels from 0 to 100 kPa in combination with 0, 10 and 20 kPa CO₂ on the respiration metabolism of greenhouse grown fresh-cut butter lettuce was studied. Controlled atmospheres of 20 or 75 kPa O₂ with 0 or 10 kPa CO₂ showed a constant respiration rate during the first 2–4 days at different temperatures (1, 5 and 9 °C). Therefore, constant respiration rates during a short period of 2–4 days could be considered as valid for a large part of the commercial life of, for instance, a modified atmosphere package development. The fresh-cut lettuce exposed to low O₂ levels (2–10 kPa) combined with moderate to high CO₂ levels (10 and 20 kPa) had a higher respiration rate than when 20–100 kPa O₂ were used. Moderate CO₂ levels (10 kPa) reduced the respiration rates of fresh-cut lettuce 20–40% at 9 °C. This effect was less noticed at lower temperatures. Gas composition with high CO₂ levels (20 kPa) probably caused a metabolic disorder increasing the respiration rate of fresh-cut butter lettuce. It was concluded that 80 kPa O₂ must be used in modified atmosphere packaging (MAP) to avoid fermentation of fresh-cut butter lettuce in combination with 10–20 kPa CO₂ for reducing their respiration rate.     

Controlled atmosphere storage of guava (Psidium guajava L.) fruit

The effects of controlled atmospheres (CA) on respiration, ethylene production, firmness, weight loss, quality, chilling injury, and decay incidence of three commercially important cultivars of guava fruit were studied during storage in atmospheres containing 2.5, 5, 8, and 10 kPa O₂ with 2.5, 5, and 10 kPa CO₂ (balance N₂) at 8 °C, a temperature normally inducing chilling injury. Mature light green fruit of cultivars, ‘Lucknow-49’, ‘Allahabad Safeda’ and ‘Apple Colour’, were stored for 30 days either in CA or normal air, and transferred to ambient conditions (25–28 °C and 60–70% R.H.) for ripening. CA storage delayed and suppressed respiratory and ethylene peaks during ripening. A greater suppression of respiration and ethylene production was observed in fruit stored in low O₂ (≤5 kPa) atmospheres compared to those stored in CA containing 8 or 10 kPa O₂ levels. High CO₂ (>5 kPa) was not beneficial, causing a reduction in ascorbic acid levels. CA storage was effective in reducing weight loss, and maintaining firmness of fruit. The changes in soluble solids content (SSC), titratable acidity (TA), ascorbic acid, and total phenols were retarded by CA, the extent of which was dependent upon cultivar and atmosphere composition. Higher amounts of fermentative metabolites, ethanol and acetaldehyde, accumulated in fruit held in atmospheres containing 2.5 kPa O₂. Chilling injury and decay incidence were reduced during ripening of fruit stored in optimal atmospheres compared to air-stored fruit. In conclusion, guava cultivars, ‘Lucknow-49’, ‘Allahabad Safeda’, and ‘Apple Colour’ may be stored for 30 days at low temperature (8 °C) supplemented with 5 kPa O₂ + 2.5 kPa CO₂, 5 kPa O₂ + 5 kPa CO₂, and 8 kPa O₂ + 5 kPa CO₂, respectively.     

1-MCP partially alleviates dehydration-induced abscission in cut leaves of the fern Nephrolepis cordifolia

Fern leaves, also called fronds, are often used in bouquets. Leaves of the sword fern (Nephrolepis cordifolia) consist of a central vascular tissue, with numerous leaflets (pinnae) at each side. Leaves that have been cut and immediately placed in water show abscission of the pinnae, starting from about day 4 of vase life, with 50% pinnae abscission on day 13. The onset of pinnae abscission was hastened by a period of dehydration (3, 6, 9 or 12 h at 25 °C). The time to 50% pinnae abscission was between 7.0 and 4.7 days after 3 h and 12 h of dehydration, respectively. Dehydration treatments might induce air emboli in the xylem, but in these experiments did not inhibit water uptake. Dehydration did increase the rate of ethylene production of the cut leaves throughout vase life. A 3 h treatment with 1-MCP at concentrations of 200 or 300 nL L^?1 prior to the period of dehydration reduced the rate of ethylene production and reduced the rate of abscission. 1-MCP treatments were also effective if given after the period of dehydration. The data show that pinnae abscission limits the vase life of cut leaves of the sword fern, and that a short period of water stress drastically increases the rate of abscission. The increase in pinnae abscission was correlated with an increase in ethylene production. As 1-MCP alleviated the effect of dehydration on pinnae abscission, the dehydration effect involved ethylene perception. The data suggest that a small water stress induced an autocatalytic rise in ethylene production which was the direct cause of the increase in pinnae abscission.     

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

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

Respiration rate response of four baby leaf Brassica species to cutting at harvest and fresh-cut washing

The influence of the first and second cutting at harvest on the physiological response of four baby leaf Brassica species was studied. The species were salad rocket (Eruca vesicaria), wild rocket (Diplotaxis tenuifolia), mizuna (Brassica rapa L. ssp. nipposinica) and watercress (Nasturtium officinale) stored at 1, 4, 8 and 12 °C. In addition, the microbial and metabolic behaviours of baby leaves were evaluated after different washing treatments including water, ozonated water (10 mg L⁻¹ total dose), ozonated water activated with ultraviolet C light (UV-C) and heat shock wash (50 °C, 1 min). Temperature had a significant effect on both respiration rate and post-cutting life. The production of CO₂ increased between 2- and 4-fold when temperature increased from 1 to 12 °C. Minor differences in leaf respiration rate between the first and second leaf cutting were observed for salad rocket and wild rocket, while leaves from the second cutting of mizuna and watercress leaves had a higher respiration rate than from the first cutting. Ozone, and ozone combined with UV-C, were the most efficient washing treatments in reducing total mesophilic counts, while heat shock treatment did not affect them. Additionally, naturally occurring Listeria spp. were controlled well in wild rocket and mizuna (<1 log cfu g⁻¹) when the ozone treatments were applied. On the other hand, respiration rates of the Brassica species were not substantially affected by the washing treatments when stored at 4 °C. Maximum CO₂ production was observed immediately after washing but decreased during the first 24 h of storage. Baby leaves washed with cold water consistently showed a lower respiration rate than the other washing treatments. Heat shock was the washing treatment that most influenced the increase in the respiration rate of baby leaves during storage at 8 °C.     

Low temperature-induced water-soaking of Dendrobium inflorescences: Relation with phospholipase D activity,thiobarbaturic-acid-staining membrane degradation products,and membrane fatty acid composition

We compared the effects of cold storage (5 °C) on two Dendrobium cultivars. After various periods of storage the cut inflorescences were transferred to 25 °C. Water-soaking of the tepals was the main chilling-injury symptom. Cv. Earsakul showed higher CI sensitivity than cv. Khao Sanan. Phospholipase D (PLD) activity increased during 5 °C storage in both cultivars, but generally increased more in cv. Earsakul during the subsequent period at 25 °C. The level of lipid degradation products (including malondialdehyde) that react with thiobarbaturic acid was higher in cv. Earsakul than in cv. Khao Sanan. In contrast to expectation, the ratio between unsaturated and saturated fatty acids was higher, and remained higher during cold storage, in cv. Earsakul than in cv. Khao Sanan. The data suggest that water-soaking due to cold storage of Dendrodium inflorescences involves membrane damage, likely related to activation of PLD and accumulation of lipid degradation products. The level of unsaturated fatty acids apparently did not protect against CI. The data seem to question the general view that unsaturated fatty acids protect against CI.     

Respiration and quality responses of sweet cherry to different atmospheres during cold storage and shipping

Most sweet cherries produced in the US Pacific Northwest and shipped to distant markets are often in storage and transit for over 3 weeks. The objectives of this research were to study the effects of sweet cherry storage O₂ and CO₂ concentrations on the respiratory physiology and the efficacy of modified atmosphere packaging (MAP) on extending shelf life. Oxygen depletion and CO₂ formation by ‘Bing’ and ‘Sweetheart’ cherry fruit were measured. While respiration rate was inhibited linearly by reduced O₂ concentration from 21% to 3–4% at 20 °C, it was affected very little from 21% to ∼10% but declined logarithmically from ∼10% to ∼1% at 0 °C. Estimated fermentation induction points determined by a specific increased respiratory quotient were less than 1% and 3–4% O₂ for both cultivars at 0 and 20 °C, respectively. ‘Bing’ and ‘Sweetheart’ cherry fruits were packaged (∼8 kg/box) in 5 different commercial MAP box liners and a standard macro-perforated polyethylene box liner (as control) and stored at 0 °C for 6 weeks. MAP liners that equilibrated with atmospheres of 1.8–8.0% O₂ + 7.3–10.3% CO₂ reduced fruit respiration rate, maintained higher titratable acidity (TA) and flavor compared to control fruit after 4 and 6 weeks of cold storage. In contrast, MAP liners that equilibrated with atmospheres of 9.9–14.4% O₂ + 5.7–12.9% CO₂ had little effect on inhibiting respiration rate and TA loss and maintaining flavor during cold storage. All five MAP liners maintained higher fruit firmness (FF) compared to control fruit after 6 weeks of cold storage. In conclusion, storage atmospheres of 1.8–14.4% O₂ + 5.7–12.9% CO₂ generated by commercial MAP, maintained higher FF, but only the MAP with lower O₂ permeability (i.e., equilibrated at 1.8–8.0% O₂) maintained flavor of sweet cherries compared to the standard macro-perforated liners at 0 °C. MAP with appropriate gas permeability (i.e., equilibrated at 5–8% O₂ at 0 °C) may be suitable for commercial application to maintain flavor without damaging the fruit through fermentation, even if temperature fluctuations, common in commercial storage and shipping, do occur.     

High CO2 effects on postharvest biochemical and textural properties of white asparagus (Asparagus officinalis L.) spears

The effects of high CO₂ concentration (10% CO₂, 17% O₂) on the changes of functional cell wall components (pectic substances, hemicellulose, cellulose, lignin), mechanical properties, content of free soluble sugars (sucrose, glucose, fructose), and respiration activity were studied in harvested white asparagus spears stored at 10 and 20 °C, respectively, for up to 7 d. Spears stored at 2, 10 and 20 °C in air were studied as controls, where the 2 °C condition indicated the effects of cold storage. During storage, respiration activity declined only slightly, irrespective of the CO₂ and temperature regime. Spears stored at 20 °C under both CA and normal air became less stiff and more elastic, however, tissue toughness increased significantly. Changes in toughness were associated primarily with the dynamics of lignin and cellulose, revealing a strong correlation (r² = 0.81). High CO₂ concentration inhibited the synthesis of cellulose and, to some extent, lignin accumulation at 20 °C. Additionally, elevated CO₂ inhibited the degradation of soluble carbohydrates. In contrast, slightly lower temperatures of 10 °C in combination with high CO₂ did not have a pronounced effect on changes in structural carbohydrates (lignin, cellulose, hemicellulose and pectins). The effect low temperature (2 °C) under normal atmosphere conditions resulted in the inhibition of cell wall changes in asparagus spears.