Chlorophyll fluorescence responds to a range of environmental stresses that affect horticultural crops. This technique has been used successfully to evaluate the quality of commodities after exposure to a number of postharvest stresses such as chilling, heat, and atmospheric stress. As well, chlorophyll fluorescence measurements have been incorporated as the main characteristics in shelf-life prediction models. Our objective was to evaluate the use of chlorophyll fluorescence measurements at harvest to predict the shelf-life of `Iceberg' lettuce. It was hypothesized that storage potential is influenced by the degree of stress induced by field conditions and that different cultivars, although grown under the same conditions, experience varying degrees of stress that can be detected by fluorescence measurements at harvest, even in the absence of visual differences in quality. The utility of fluorescence measurements was limited by inconsistencies in the development of the heads, such as maturity and leaf formation, and by variation among different areas of the same leaf. Fluorescence data from a homogeneous group of heads revealed that the variation associated with different areas of the same leaf was larger than that associated with measurements from different heads. Also, fluorescence readings from one leaf differed from those taken from any non-adjacent leaves. These sources of variation, along with strong cultivar-dependant differences in the fluorescence signal, were quite large, and hence, any trends in fluorescence measurements related to storage potential were not observed. Therefore, chlorophyll fluorescence at harvest does not appear to be a good predictor of lettuce storability.
R. Andrew Schofield, Jennifer R. DeEll and Dennis P. Murr
H.P. Vasantha Rupasinghe, Gopinadhan Paliyath and Dennis P. Murr
To decipher the relation between α-farnesene metabolism and the development of superficial scald in apples, trans,trans-α-farnesene synthase, the enzyme that catalyzes the conversion of farnesyl pyrophosphate to α-farnesene, was partially purified from skin tissue of `Delicious' apples (Malus ×domestica Borkh.) and characterized. Total and specific activities of the enzyme were higher in the cytosolic fraction than in membrane fractions. α-Farnesene synthase was purified 70-fold from the cytosolic fraction by ion exchange chromatography and gel permeation, and the native molecular weight was estimated to be 108,000. The enzyme had optimal activity at a pH of 5.6 and absolutely required a divalent metal ion such as Mg2+ or Mn2+ for activity. It exhibited allosteric kinetics, S(0.5) for farnesyl pyrophosphate being 84±18 μmol·L-1, and a Hill coefficient (nH) of 2.9, indicating the number of subunits to be two or three. Enzyme activity was highest between 10 and 20 °C, while 50% of the maximal activity was retained at 0 °C. In vivo α-farnesene synthase activity was minimal at harvest, then increased rapidly during 16 weeks storage in air at 0 °C, and decreased during further storage. Activity of α-farnesene synthase, α-farnesene content, and conjugated triene alcohol (the putative scald-causing oxidation product of α-farnesene) content in skin tissue were not correlated to the inherent nature of scald susceptibility or resistance in 11 apple cultivars tested.
Jennifer R. DeEll, Robert K. Prange and Dennis P. Murr
Chlorophyll fluorescence, measured using a Plant Productivity Fluorometer Model SF-20 (Richard Brancker Research, Ottawa, Ont.), was evaluated as a rapid and nondestructive technique to detect low O2 and/or high CO2 stress in apples during storage. `Marshall' McIntosh apples were held for 5, 10, 15, 20, or 25 days at 3C in the following four treatments: standard O2 (2.5% to 3%) and low CO2 (<1%); low O2 (1% to 1.5%) and low CO2 (<1%); standard O2 (2.5% to 3%) and standard CO2 (4% to 4.5%); or standard O2 (2.5% to 3%) and high CO2 (11% to 12%). Only 10% of the apples had skin discoloration after 5 days in 1% to 1.5% O2, while 80% developed skin discoloration after 20 days in low O2. Small desiccated cavities in the cortex, associated with CO2 injury, developed in 10% of the apples after 20 days in 11% to 12% CO2. Both 1% to 1.5% O2 and 11% to 12% CO2 for 5 days caused chlorophyll fluorescence [Fv = (P – T)/P] of apple fruit to decrease, as compared to those held in standard atmospheres. Additional exposure time did not significantly affect Fv in either the low-O2 (1% to 1.5%) or high-CO2 (11% to 12%) treatment. The results of this study suggest that chlorophyll fluorescence can detect low-O2 and high-CO2 stress in apples, prior to the development of associated physiological disorders.
Rodger Tschanz, Dennis Murr, Len Wiley and Kay Hustwit
The use of chemical thinners is an essential component of commercial apple production in Ontario. As chemical thinning options decrease, due to environmental concerns, newer and less toxic alternatives must be found. Benzyladenine (BA), available in the United States as Accel, shows promise as a thinning agent. During the 1994 growing season, Accel was applied under commercial conditions to seven apple cultivars—`McIntosh' (spur), Delicious `Starkrimson', `Empire', `Jonagold', `Golden Delicious', `Jonamac', and Gala `Royal Gala'. Application concentrations ranged from 50 to 75 ppm (a.i. BA), depending on cultivar. Mean king fruitlet diameter at time of application ranged from 9 to 12 mm. The thinning response of Accel was compared with that of traditional chemical (e.g., carbaryl, NAA, or both) or mechanical thinning treatments. At the concentrations used in this experiment, thinning with Accel was comparable or better than traditional methods in the case of `Gala', `Jonagold', `Empire', and `Golden Delicious'. In those cultivar trials displaying an acceptable Accel thinning response, a significant fruit size increase also was observed.
Lisa J. Skog*, Theo Blom, Wayne Brown, Dennis Murr and George Chu
Ozone treatment has many advantages for control of fungal diseases. There are no residue concerns, no registration is required, and it is non-specific, therefore potentially effective against a broad spectrum of pathogens. However, ozone is known to cause plant damage. There is little information available on either the ozone tolerance of floriculture crops or the levels required to kill plant pathogens under commercial conditions. Nine floriculture crops (begonia, petunia, Impatiens, Kalanchoe, pot roses, pot chrysanthemums, lilies, snapdragons and Alstroemeria) were subjected to increasing levels of ozone. Trials were conducted at 5 and 20 °C (90% to 95% RH) and ozone exposure was for 4 days for either 10 hours per day (simulating night treatment) or for 10 minutes every hour. Damage was assessed immediately after treatment and after an additional 3 days at room temperature in ozone-free air. Trials were terminated for the crop when an unacceptable level of damage was observed. Trials to determine the lethal dose for actively growing pathogens (Alternaria alternata, Alternaria zinniae and Botrytis cinerea) and fungal spores were conducted under identical conditions. Ozone tolerance varied with plant type and ranged between <0.2 and 3ppm. Generally, the crops surveyed were more susceptible to ozone damage at the low temperature. As a group, the bedding plants were the least tolerant. Fungal spores were killed at treatment levels between 0.8 and 2 ppm ozone. The actively growing fungal mycelium was still viable at 3 ppm ozone when the trial had to be terminated due to ozone-induced structural damage in the treatment chambers. Under the trial conditions, only the Kalanchoe would be able to tolerate the high levels of ozone required to kill the fungal spores.
Harmander Pal Singh*, Dennis P. Murr, Gopi Paliyath and Jennifer R. DeEll
`Gala' apples (Malus × domestica Borkh) were harvested at optimum maturity for long-term storage, precooled overnight at 0 °C, treated with 1 μL·L-1; 1-methylcyclopropene (1-MCP) for 24 hours at 0 °C, and then placed in controlled atmosphere (CA) to determine the storage regime that would have the least negative impact on post-storage aroma volatile production. Fruit were stored at 0° and 2.5° C in ultra low oxygen (0.6% O2 -0.6% CO2; ULOCA), low oxygen (1.2% O2 -1.2% CO2; LOCA) and standard (2.5% O2 -2.5% CO2; SCA) CA for 120 and 240 days, and in ambient air for 60, 90, 120 and 150 days. Post-storage fruit volatiles were quantified by headspace analysis using a solid-phase micro-extraction (SPME) probe and FID-GC, and key volatiles were identified by GC-MS. Fruit volatile production was greatest at harvest, and decreased thereafter for fruit held in air and CA for up to 150 or 240 days, respectively. 1-MCP treatment resulted in reduced rates of respiration, ethylene and volatile production, regardless of storage regime, and resulted in a reduced production rate of all the major volatile compounds, including esters, alcohols, acids, aldehydes and ketones. Post-storage volatile production was the least in fruits removed from 0 °C in ULO, followed by LO, SCA, and then air. 1-MCP treatment inhibited post-storage volatile production in CA- and air-stored fruit by as much as 95 percent. However, recovery of aroma was delayed significantly in fruit which had been held at 0 °C vs. 2.5 ° C, suggesting aroma volatile synthesis in `Gala' is chilling sensitive.
H.P. Vasantha Rupasinghe*, Dennis P. Murr, Jennifer R. DeEll and Joseph Odumeru
Wounding during processing triggers physiological reactions that limits shelf-life of fresh-cut apples. Exposure of `Empire' and `Crispin' apples at harvest to the ethylene antagonist 1-methylcyclopropene (1-MCP, SmartFresh™) on the maintenance of fresh-cut apple quality was evaluated in combination with post-cut dipping of NatureSeal™. Efficacy of 1-MCP on fresh-cut physiology and quality depended on the storage duration and apple cultivar. Ethylene production and respiration of apple slices were inhibited by 1-MCP but not by NatureSeal. Total volatiles produced by fresh-cut apples was not affected by the treatments. 1-MCP influenced the quality attributes of fresh-cut apple slices prepared from apples stored either 4 months in cold storage or 6 months in controlled atmosphere. Enzymatic browning and softening of the cut-surface, total soluble solids, and total microbial growth were suppressed by 1-MCP in `Empire' apples. Overall, the influence of 1-MCP on quality attributes in `Crispin' apple slices was marginal. NatureSeal consistently maintained the firmness of fresh-cut apple slices held at 4 °C for up to 21 days. The additive effect of 1-MCP in the maintenance of apple quality is an advantage for processing and marketing of fresh-cut apples.
Dan D. MacLean, Dennis P. Murr, Jennifer R. DeEll and Eugene Kupferman
The ethylene antagonist 1-methylcyclopropene (1-MCP) was investigated for its potential impact on the transcription of key flavonoid biosynthetic (PAL and CHS) and ethylene perception (ERS1) genes during the postharvest storage of pear (Pyrus × communis L.). Optimally harvested red and green `d'Anjou' fruit were treated with 1 μL·L-1 1-MCP for 24 h at 0 °C to 1 °C, and subsequently placed in cold storage (0–1 °C, 90–95% RH). Fruit were removed every 21 days for 126 days, and evaluated for firmness, TSS, and ethylene and volatile production for up to 10 days (≈21 °C). Tissue samples were collected for Northern blot analysis and determination of flavonoid and chlorogenic acid content. PAL content increased during the 1-week simulated marketing period irrespective of storage duration, which coincided with an increase in respiration and ethylene content. Although it was still detectable, total PAL content was dramatically reduced by the 1-MCP treatment. CHS was abundant immediately after harvest and after removal from storage, but declined rapidly thereafter, and was not detectable after 1 week at room temperature. The 1-MCP treatment further exacerbated this decreasing trend in CHS content. ERS1 content appears to be stable throughout storage and the simulated marketing period, with levels lower in 1-MCP-treated fruit. These results suggest that 1-MCP significantly inhibits the transcription of key flavonoid and ethylene regulatory enzymes, possibly compromising the nutraceutical content of pear fruit. The increase in PAL with the concomitant decrease of CHS after removal from storage suggests a diversion of carbon from flavonoid compounds into simple phenols, such as chlorogenic acid.
John T.A. Proctor, Dennis P. Murr and E.C. (SAM) Lougheed
H.P. Vasantha Rupasinghe, Dennis P. Murr, Jennifer R. DeEll and Murray D. Porteous
Flesh softening is a major quality parameter that can limit long-term storage of apple cultivars. This study investigated the combined effects of preharvest AVG (Retain™) application, 1-methylcyclopropene (1-MCP; EthylBloc™) exposure at harvest, and commercial controlled atmosphere (CA) storage (2.0% O2 + 2.5% CO2) on flesh softening of `Empire' apple. Treatments were assigned in a split-split-plot experimental design; AVG and no AVG application as the main-plot, CA and air storage as the sub-plots, and 0, 0.1 0.5, 1.0 mL·L–1 1-MCP as the sub-sub-plots. Apples were removed from storage at 70 and 140 days after harvest and kept up to an additional 2 weeks at 20 °C for post-storage assessment of ripening. Preharvest AVG application of `Empire' fruit delayed maturation slightly as determined by starch index at harvest, but did not affect fruit size at harvest nor flesh softening in storage. All levels of 1-MCP were equally effective in controlling fruit softening both in air and CA, as 1-MCP-treated fruit were ≈2.5 kg firmer than untreated fruit. This firmness advantage was still evident even after 2 weeks at 20 °C, with CA-stored fruit holding their firmness the best. When all three technologies were combined, treated fruit were overall 156% firmer than control fruit (no AVG, no 1-MCP, air-stored). As well, ethylene production and emanation of aroma volatiles were reduced significantly in these fruit. Therefore, the synergism of AVG, 1-MCP and long-term CA storage could potentially hold flesh firmness and other ripening parameters of apples to values near those found at harvest.