Experiments were conducted to determine if ethylene influences chilling injury, as measured by percentage of slices exhibiting water-soaked areas in fresh-cut tomato slices of `Mountain Pride' and `Sunbeam' tomato (Lycopersicon esculentum Mill.). Ethylene concentration in containers without ventilation significantly increased during storage at 5 °C, whereas little or no accumulation of ethylene occurred in containers with one or six perforations. Chilling injury was greatest for slices in containers with six perforations, compared to slices in containers with one perforation, and was over 13-fold greater than that of slices in control containers with no perforations. An experiment was also performed to investigate the effectiveness of including an ethylene absorbent pad in containers on subsequent ethylene accumulation and chilling injury. While ethylene in the no-pad controls increased continually during storage of both `Mountain Pride' and `Sunbeam' tomatoes at 5 °C under modified atmosphere conditions, no increase in accumulation of ethylene was observed in containers containing ethylene absorbent pads throughout storage. The ethylene absorbent pad treatment resulted in a significantly higher percentage of chilling injury compared with the no-pad control. In studies aimed at inhibiting ethylene production using AVG during storage of slices, the concentration of ethylene in control containers (no AVG) remained at elevated levels throughout storage, compared to containers with slices treated with AVG. Chilling injury in slices treated with AVG was 5-fold greater than that of controls. Further, we tested the effect of ethylene pretreatment of slices on subsequent slice shelf life and quality. In slices treated with ethylene (0, 0.1, 1, or 10 μL·L-1) immediately after slicing, ethylene production in nontreated controls was greater than that of all other ethylene pretreatments. However, pretreatment of slices 3 days after slicing resulted in a different pattern of ethylene production during storage. The rate of ethylene production by slices treated with 1 μL·L-1 ethylene 3 days after slicing was greater during storage than any of the other ethylene treatments. With slices pretreated with ethylene, both immediately and 3 days after slicing, the rate of ethylene production tended to show a negative correlation with chilling injury. Chemical name used: 1-aminoethoxyvinylglycine (AVG).
Ji Heun Hong and Kenneth C. Gross
Y.J. Yang and K.A. Lee
Garlic (Allium stivum L. cv. `Seosan') grown in Kyungbuk, Korea were harvested on June 1999 and dried in the field for 2 to 3 days. Bulbs were selected for uniformity in size and maturity and divided into two groups. One group was further dried in the shade at 25 °C for curing before storage at 0 °C. The other group was stored at 0 °C immediately without additional drying. Respiration of garlic bulbs dried additionally for 3 months was low, ranging from 1.5 to 3.0 CO2 mL/kg per h for 95 days in storage; ethylene was not detected until 60 days in storage. Non-curing samples showed rapid increase of carbon dioxide production after 50 days of storage, this might be related to incidence of fungal decay. Ethylene showed maximum value at 45 days in storage, thereafter remained level of 5.6-6.3 μL/kg per h. All treatments did not show sprouting during storage period, but incidence of decay was significantly reduced by additional drying. The beneficial effect of curing for 3 months at 25 °C was maintenance of low water content in garlic bulbs, which resulted in reduction of decay.
Mark A. Ritenour, Carlos H. Crisosto, Guiwen W. Cheng, and David T. Garner
The development of ethylene preconditioning treatments for kiwifruit have made it possible to deliver ripe kiwifruit to consumers early in the season. We report on how maturity and length of storage time affect the ripening responses of kiwifruit [Actinidia deliciosa (A Chev) Liang et Ferguson cv Hayward] preconditioned with 100 ppm ethylene at 0°C for 24 hours and ripened for 10 days at 20°C. Kiwifruit freshly harvested at weekly intervals continued to soften faster in response to ethylene preconditioning compared to air controls for at least 5 weeks following commercial harvest. In contrast, kiwifruit commercially harvested and stored at 0°C for more than 2 weeks no longer responded to low-temperature ethylene preconditioning. However, kiwifruit stored more that 5 weeks were still responsive to exogenous ethylene and softened faster when exposed to continuous ethylene at either 0 or 20°C. Kiwifruit had relatively high respiration rates 1 days after transferring from 0 to 20°C, which quickly dropped to base levels within 1 day. Fruit stored >1 week at 0°C always had higher initial respiration than freshly harvested fruit on transfer to 20°C, and ethylene preconditioning increased initial respiration of freshly harvested fruit but had less of an effect on initial respiration of stored fruit. Plotting firmness against individual fruit's respiration and ethylene production revealed a distinct rise in respiration and ethylene production only after fruit softened to <6.5 N. Preconditioning fruit at 0°C did not significantly alter the timing of the climacteric respiration or ethylene peaks.
Ahmed F. El-Shiekh, Cindy B.S. Tong, James J. Luby, and Emily E. Hoover
The relationships between cellular characteristics of cortical tissue and changes in texture during storage under controlled atmosphere (CA, 3% O2 + 3% CO2) or air at 0C were studied. The cultivars used were `Delicious', `Cortland', `Honeycrisp' and its parents, `Honeygold' and `Macoun'. The force needed to break a 7-mm cylinder of apple flesh (breaking force) was greatest for `Delicious' and `Honeycrisp'. Scanning electron microscopy demonstrated that tissues of firm-fleshed cultivars (`Honeycrisp' and `Delicious') fractured through cells, while that of soft-fleshed cultivars (`Cortland', `Honeygold', and `Macoun') fractured between cells. `Honeycrisp' had fewer cells/100 cm2 than the other cultivars. After 9 months of storage, breaking force, cell size, and K+/Ca2+ decreased, while cell number/100 cm2, Ca2+ content, and K+ content increased for all cultivars. Cell number/100 cm2 was significantly less and breaking force was significantly greater for tissue from CA than air-stored fruit.
L.J. Skog, R.B. Smith, and D.P. Murr
`Fantasia' nectarines (Prunus persica L.Batsch) were either stored immediately at 0.5C or subjected to a 48-h delay at 20C in air or with 5% CO2 in air before storage. Samples were evaluated at harvest and after 18, 25, 32, 39 and 46 days storage in air or in 5% O2 with 0%, 4%, 8%, or 12% CO2. All samples were evaluated at optimum ripeness. A combination of delayed storage and elevated CO2 in storage effectively delayed chilling injury (CI) symptoms. Control of CI increased with increasing CO2 level in delayed and nondelayed treatments. Delayed storage was not effective without elevated levels of CO2 in the storage atmosphere. Fruit that was stored without delay did not soften normally during the ripening period and developed a dry, rubbery texture. The effect was enhanced as CI progressed, resulting in increased firmness of ripened fruit with increased storage time. The delayed storage treatments softened normally during ripening, but CI fruit had a dry, mealy texture. Internal conductivity measurements correlated well with CI development. Off-flavors were detected at the higher levels of CO2 storage.
Lihua Fan, Jun Song, Charles F. Forney, and Michael A. Jordan
Ethanol concentration and chlorophyll fluorescence (CF) were measured as signs of heat stress in apple fruit [Malus sylvestris (L.) Mill. var. domestica (Borkh.) Mansf.]. `McIntosh', `Cortland', `Jonagold', and `Northern Spy' apples were placed in trays and exposed to 46 °C for 0, 4, 8, or 12 hours. Following treatments, fruit were stored in air at 0 °C and evaluated after 0, 1, 2, or 3 months. Ethanol and ethylene production, CF, peel and flesh browning, firmness, skin color, soluble solids, and titratable acidity were measured. Increases in ethanol were apparent immediately following 12-hour heat treatments as well as after 3 months. After 3 months, ethanol concentrations were 16-, 52-, 6-, and 60-fold higher in `McIntosh', `Cortland', `Jonagold', and `Northern Spy' apples than in controls, respectively. The concentrations of ethanol accumulated reflected the degree of heat-induced fruit injury. Heat treatments reduced ethylene production relative to control values. After 3 months of storage ethylene production of fruit exposed to 46 °C for 12 h was <0.48 μmol·kg-1·h-1 compared to >4.3 μmol·kg-1·h-1 for controls. Heat treatments also reduced CF which was expressed as Fv/Fm, where Fv is the difference between the maximal and the minimal fluorescence (Fm - Fo), and Fm is the maximal fluorescence. After 3 months storage at 0 °C, Fv/Fm was ≈0.2 in fruit held at 46 °C for 12 hours compared with 0.5-0.6 for control fruit. Exposure to 46 °C for 12 hours caused severe peel and flesh browning in all cultivars. Severity of peel and flesh browning increased with increasing duration of heat treatment and subsequent storage at 0 °C. `Northern Spy' apple fruit were most susceptible to heat stress based on the degree of flesh browning. Heat treatments of 8 and 12 hours reduced firmness of `McIntosh', `Cortland', and `Northern Spy', but not `Jonagold' apples. Hue angle of the green side of fruit was also reduced in `Cortland', Jonagold' and `Northern Spy' apples receiving the 8- and 12-hour treatments. Heat treatments caused a decrease in fruit tiratable acidity, but had no effect on soluble solids content. The increase in ethanol production and decrease in CF correlated with heat-induced injury, and were apparent before browning was visually apparent. Ethanol and CF have the potential to be used to nondestructively predict the severity of injury that develops during storage.
Philip L. Forsline, James R. McFerson, and Warren F. Lamboy
The USDA–ARS active collection of Malus includes over 2500 accessions maintained as field-grown trees at the Plant Genetic Resources Unit (PGRU), Geneva, N.Y. Nearly 30% of this collection is presently cryopreserved as dormant buds at the National Seed Storage Laboratory, Fort Collins, Colo., as a backup security collection. Successful bud-grafting recovery rates (≥40%) after one to four years of cryogenic storage have been documented for over 675 of 750 accessions tested. However, current protocols dictate budwood collection at PGRU from late December through early March, when buds are thought to be optimally acclimated for desiccation and slow freezing to –30°C, our pretreatment for cryopreservation. This causes a processing bottleneck. Our observations suggest temporary storage of budwood at –4°C after field harvest is possible, but we had not tested this directly. Therefore, we collected budwood from four accessions representing different levels of cold tolerance on six dates from January to March, 1995. Dormant buds were processed for cryopreservation monthly after storage in sealed bags at –4°C for 1 to 6 months. Recovery rates ranged from 55% to 100%. Neither collection date nor length of storage at –4°C affected rate of recovery. These results suggest we can significantly increase the throughput and efficiency of our cryopreservation efforts, thereby enhancing management and security of the Malus collection.
Mark P. Kaczperski, Allan M. Armitage, and Pamela M. Lewis
Seed of Petunia × hybrida `Ultra White' were germinated in #406 plug trays at 2.5 C and at a light intensity of 100 μ mol s-1m-2 using a 24 or photoperiod. At germination, seedlings were grown under natural light conditions for 8 hrs (SD) or for 8 hrs with the photoperiod extended to 16 hrs (LD) using incandescent bulbs. At approximately the 6th leaf stage, seedlings were stored at 5 C in the dark or at 12 μ mol s-1m-2 and a 24 hr photoperiod for 0 to 21 days. After storage, plants were potted n 10 cm pots and grown to flowering in a greenhouse. Plants grown under SD to the 6th leaf stage with no cold treatment were shorter. flowered later and had more lateral branching than unstored LD plants. Storage at 5 C decreased time to flower of SD plants and increased branching of LD plants regardless of photoperiod during storage.
Allan M. Armitage, Linda Copeland, Paula Gross, and Meg Green
Rhizomes of Oxalis adenophylla Gillies and bulbs of Ipheion uniflorum Raf. were planted and wet- or dry-stored at 5 °C for 0, 6, 10, 14, or 18 weeks, before being placed in a greenhouse. Regardless of moisture regime, foliage emergence and time to flower decreased for both species with increasing duration of cooling. Wet-stored bulbs/rhizomes within a cooling treatment required less time to foliage and flower emergence when compared with the corresponding dry-storage period. About 10 weeks of 5 °C was optimum for both species.
Shirin Shahkoomahally and Asghar Ramezanian
). According to our review, there is no report on postharvest application of Ca and hot water on qualitative parameters of kiwifruit during cold storage. The overall aim of this research was to evaluate the effect of hot water combined with Ca solution