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.     

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.     

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.     

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.     

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.     

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.     

Genotypic differences in post-storage photosynthesis and leaf chloroplasts in response to ethylene and 1-methylcyclopropene in Aglaonema

This study investigated the effects of ethylene in storage and 1-methylcyclopropene (1-MCP) pretreatment on post-storage leaf senescence as measured by changes in photosynthesis and chloroplast degradation of two Aglaonema cultivars. Potted plants of ‘Chalit's Fantasy’ and ‘White Tip’ with or without 1-MCP treatment (600 nL L⁻¹ 1-MCP for 6 h) were exposed to 3.0 μL L⁻¹ ethylene, while being stored for 5 d at 16 °C in the dark, and then placed under an indoor environment for further observation. Plants that did not receive 1-MCP and ethylene served as controls. Ethylene did not affect the stomatal conductance in either cultivar. Ethylene reduced the net CO₂ assimilation rate and F_v/F_m (potential photochemical efficiency of photosystem II) in ‘White Tip’, but not in ‘Chalit's Fantasy’. Chloroplast number in a palisade or spongy mesophyll cell did not differ among treatments in ‘Chalit's Fantasy’. However, ethylene-treated ‘White Tip’ had fewer chloroplasts in the mesophyll cells, had more and larger plastoglobules in the chloroplasts, and had looser granal stacking with enlarged thylakoid lumens. ‘Chalit's Fantasy’ plants that were treated with 1-MCP before exposure to ethylene had higher net CO₂ assimilation rates and stomatal conductance than the control or plants that were exposed to ethylene without 1-MCP pretreatment. 1-MCP pretreatment mitigated the injurious effect of ethylene on ‘White Tip’ by increasing net CO₂ assimilation rate and F_v/F_m, and maintaining the quantity and structural integrity of chloroplasts.     

Postharvest physiology and volatile production by flowers of Ptilotus nobilis

Ptilotus nobilis (Lindl.) F. Muell. has potential in the floriculture industries as a cut flower crop. Ethylene production and respiration rates, fresh weight changes and volatile scent production from cut inflorescences of P. nobilis cultivars Passion (dark pink flowers) and Purity (white-green flowers) were measured during vase life. Inflorescence weight loss was significant (P < 0.001) during vase life with wilting and colour loss being the primary reasons for loss of vase life. Inflorescences ready for the cut market stored and at 22 °C had vase lives of >12 d. Ethylene production by inflorescences was low to negligible. Treatment with silverthiosulphate (STS) and ethylene had no effects on vase life. Evidently, ethylene did not play a role in determining the postharvest longevity of cut P. nobilis flowers. Respiration rates of inflorescences were high at harvest (>700 mg CO₂ kg⁻¹ FW h⁻¹) and declined gradually thereafter during vase life. Total volatile emissions followed a similar pattern. For Passion, respiration rates of immature florets were significantly greater (P = 0.02) than florets from other developmental stages while the calyx produced the most CO₂. For Purity, respiration rates of florets of different maturities did not differ and the reproductive tissue produced the most CO₂. Only fully opened mature florets with their stigma and anthers revealed, emitted significant quantities of volatiles (P < 0.001) and primarily from the calyx tissue for both cultivars. The individual volatiles differed somewhat for the two cultivars. However, both produced significant quantities of benzaldehyde, 3,5-dimethoxytoluene and benzyl alcohol. These compounds have previously been associated with desirable floral scent.     

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.     

Ripening and sensory analysis of Guatemalan-West Indian hybrid avocado following ethylene pretreatment and/or exposure to gaseous or aqueous 1-methylcyclopropene

Previous reports showed that both gaseous and aqueous 1-methylcyclopropene (1-MCP) delay ripening of avocado (Persea americana Mill.), but there are no reports of the influence of 1-MCP on its sensory attributes. The objective of this study was to evaluate the effects of ethylene pretreatment and/or exposure to gaseous or aqueous 1-MCP on fruit ripening and sensory attributes of ‘Booth 7’ avocado, a Guatemalan-West Indian hybrid. Separate experiments were conducted during two seasons (2008 and 2009) with fruit harvested at preclimacteric stage in October (early season) and in November (late season). Fruit from Season 1 were exposed to ethylene (4.07 μmol L⁻¹) for 12 h at 20 °C, and stored for more 12 h at 20 °C in an ethylene-free (ethylene, <0.1 μL L⁻¹) room prior to treatment with either aqueous (1.39 or 2.77 μmol L⁻¹ a.i.) or gaseous (3.15 or 6.31 nmol L⁻¹ a.i.) 1-MCP. Ripening was monitored and firmness, respiration, ethylene production and weight loss were measured. Texture profile analysis and sensory analysis were performed on ripe fruit only (firmness, 10–15 N). Fruit from Season 2 were not exposed to ethylene pretreatment but treated only with aqueous 1-MCP 24 h after harvest. Fruit were assessed exclusively for sensory analysis when ripe (firmness, 10–15 N). Treatment with either 1-MCP formulation effectively delayed ripening from 4 to 10 d for early-season fruit, and from 4 to 6 d for late-season fruit. Higher concentrations of 1-MCP of either formulation had the greatest effect on selected pulp textural parameters of early-season fruit; the gaseous formulation had greater effect on late-season fruit quality than the aqueous formulation. In general, sensory panelists ratings of overall liking were not affected by 1-MCP treatment. Both aqueous and gaseous 1-MCP formulations delayed ripening of the Guatemalan-West Indian ‘Booth 7’ avocado without significant loss in appearance or in sensory attributes and, therefore, could be considered for use as a postharvest treatment for this hybrid.     

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.     

The effects of ethylene, 1-MCP and AVG on sprouting in sweetpotato roots

Exogenous ethylene is commonly used as a commercial sprouting inhibitor of potato tubers. The role of ethylene in the control of sprouting of sweetpotato roots, however, is not known. The aim of this study was to investigate the role of ethylene in control of sprouting in sweetpotato roots by observing the effect of an ethylene synthesis inhibitor, aminoethoxyvinylglycine (AVG), and the ethylene antagonist, 1-methylcyclopropene (1-MCP), in the presence and absence of exogenous ethylene on root sprouting and associated sugar accumulation. Continuous exposure to 10 μl L⁻¹ ethylene, 24 h exposure to 625 nl L⁻¹ 1-MCP or dipping in 100 μl L⁻¹ AVG all inhibited sprout growth in sweetpotato roots of two varieties over 4 weeks of storage at 25 °C. The observations that both ethylene on its own and 1-MCP, which inhibits ethylene action, inhibit sprout growth indicate that while continuous exposure to exogenous ethylene leads to sprout growth inhibition, ethylene is also required for sprouting. In potato tubers ethylene is required to break dormancy, while continuous exposure inhibits sprout growth.Monosaccharide concentrations in ethylene, 1-MCP or AVG treated roots were lower than in untreated roots, and for ethylene treated roots this was associated with higher respiration rates. This is consistent with the activation of some additional process by ethylene which uses energy through sugar metabolism. 1-MCP and AVG both inhibited this increase in respiration rate and counteracted the decrease in monosaccharide concentrations. 1-MCP presumably counteracts the ethylene stimulation of this process, while the effect of AVG is attributed to its possible inhibitory effects on protein synthesis.     

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.     

Response of climacteric-type guava (Psidium guajava L.) to postharvest treatment with 1-MCP

Guava (Psidium guajava L. cv. ‘Allahabad Safeda’) fruit harvested at the mature light-green stage were exposed to 300 and 600 nL L⁻¹ 1-methylcyclopropene (1-MCP) for 6, 12 and 24 h at 20 ± 1 °C, and held in either cold storage (10 °C) for 25 days or ambient conditions (25–29 °C) for 9 days. Most of the physiological and biochemical changes during storage and ripening were affected by 1-MCP in a dose dependent manner. Ethylene production and respiratory rates were significantly suppressed during storage as well as ripening under both the storage conditions depending upon 1-MCP concentration and exposure duration. 1-MCP treatment had a pronounced effect on fruit firmness changes during storage under both the conditions. The reduced changes in the soluble solids contents (SSC), titratable acidity (TA) and vitamin C content showed the effectiveness of 1-MCP in retarding fruit ripening. Vitamin C content in 1-MCP-treated fruit was significantly higher than in non-treated fruit, and those treated with 300 nL L⁻¹ 1-MCP for 6 h. The development of chilling injury symptoms was ameliorated to a greater extent in 1-MCP-treated fruit during cold storage and ripening. A significant reduction in the decay incidence of 1-MCP-treated fruit was observed under both the storage conditions. 1-MCP at 600 nL L⁻¹ for 12 h, in combination with cold storage (10 °C) seems a promising way to extend the storage life of guava cv. ‘Allahabad Safeda’ while 1-MCP at 300 nL L⁻¹ for 12 and 24 h or 600 nL L⁻¹ for 6 h, may be used to provide 4–5 days extended marketability of fruit under ambient conditions.     

Effect of 1-methylcyclopropene (1-MCP) on softening of fresh-cut kiwifruit,mango and persimmon slices

Ethylene production is enhanced by wounding during fresh-cut processing and the accumulation of this gas within the packages of fresh-cut fruit can be detrimental to their quality and shelf-life. The effect of 1-methylcyclopropene (1-MCP), an ethylene action blocker, applied before or after processing, on the quality of fresh-cut kiwifruit, mangoes and persimmons was evaluated during storage at 5 °C. Fresh-cut ‘Hayward’ kiwifruit slices softened at a slower rate and their ethylene production rate was decreased in response to 1-MCP application (1 μL L⁻¹ for 6 h at 10 °C) either before or after processing. A 2-min dip in 0.09 M (1%, w/v) CaCl₂ synergistically increased the effect of 1-MCP on firmness retention and 1-MCP did not affect the color (L* value) of fresh-cut kiwifruit slices. Softening and browning (decreasing L* value) were delayed when 1-MCP was applied directly on fresh-cut ‘Kent’ and ‘Keitt’ mango slices. Respiration rate of mango slices was not influenced by 1-MCP whereas the ethylene production was affected only towards the end of their shelf-life. Fresh-cut ‘Fuyu’ persimmons treated with 1-MCP after processing presented higher ethylene production rate, slower softening rate and slower darkening of color (decrease in L* value), whereas the respiration rate was not affected.     

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.     

Apparent synergism between the positive effects of 1-MCP and modified atmosphere on storage life of banana fruit

Fruit of cv. Gros Michel banana were treated with 1-MCP (1000 nL L⁻¹ for 4 h at 25 °C) and then packed in non-perforated polyethylene (PE) bags for modified atmosphere storage (MAP). The bags were placed in corrugated cardboard boxes and stored at 14 °C. Fruit were removed from cool storage and ripened at room temperature using ethephon. The length of storage life was determined by the change in peel color to yellow, after this ethephon treatment. Fruit treated with 1-MCP + MAP had a storage life of 100 days. The storage life of control fruit (no 1-MCP and no MAP) was 20 days. Fruit held in PE bags without 1-MCP treatment had a 40 day storage life, and the same was found in fruit treated with 1-MCP but without PE bags. 1-MCP is an inhibitor of ethylene action, but also inhibited ethylene production, mainly through inhibition of ACC oxidase activity in the peel. MAP inhibited ethylene production mainly through inhibition of ACC oxidase, both in the peel and pulp. The combination of 1-MCP treatment and MAP storage resulted in much lower ethylene production due to inhibition of both ACC synthase and ACC oxidase activity.     

Sucrose feeding of Cut Dendrobium inflorescences promotes bud opening,inhibits abscission of open flowers,and delays tepal senescence

Inflorescences of Dendrobium cv. Khao Sanan were held in distilled water (controls) or in solutions containing two antimicrobial compounds (silver nitrate and 8-hydroxyquinoline sulfate) with or without 4 g L⁻¹ sucrose or 4 g L⁻¹ glucose. Sugar + antimicrobial compounds promoted bud opening and largely prevented abscission of open flowers. It also resulted in a delay of tepal senescence. No clear effect was found of sucrose feeding on the concentrations of sucrose, glucose and fructose in the tepals of open flowers, but an increase in sucrose, glucose, and fructose concentrations was found in the column + labellum. It is concluded that the effect of sugar feeding on abscission and tepal senescence might relate to a reduction of ethylene sensitivity. It was previously concluded that tepal senescence in Dendrobium flowers was not regulated in the tepals but in the column. It is not clear how the increased in sugar levels in the column + labellum relates to the delay of tepal senescence after sugar feeding.