Responses to temperature of fruit dry weight,oil concentration,and oil fatty acid composition in olive (Olea europaea L. var. ‘Arauco’)

Correlative studies in olive using data from different locations or years suggest that temperature can modulate crop oil yield and oil composition. However, there are no published studies of manipulative experiments that demonstrate a direct role for temperature as a regulator of oil yield and oil quality in olive. The objectives of this study were to: i) elucidate the effect of temperature during the fruit oil accumulation phase on fruit dry weight, oil concentration and fatty acid composition; and ii) identify the developmental window within the oil accumulation phase exhibiting the greatest sensitivity to temperature and that with the highest fruit capacity to recover from the temperature treatments. Two branch-level experiments were conducted in a commercial orchard at Los Molinos (La Rioja, Argentina) using var. ‘Arauco’. Both experiments were conducted during the oil accumulation phase by enclosing fruiting branches in transparent plastic chambers with individualized temperature control. The first experiment; known as the four month long experiment, employed four temperature treatments that were applied for a single period of four months: a control at ambient temperature, two heating levels (5 °C and 10 °C warmer than the control), and a cooling level (5 °C cooler than the control). The second experiment consisted of four separate successive one month long treatment periods, in each of which two temperature treatments were applied: control and heating (ca. 7 °C higher than control). In the four month long experiment, fruit dry weight was not affected by average temperatures in the 16–25 °C range, but it was reduced with further increases in temperature. Oil concentration decreased linearly at 1.1% °C⁻¹ across the whole range (16–32 °C) of average seasonal temperatures explored, while oleic acid concentration decreased 0.7% °C⁻¹ over the same range. In the one month long experiment, 30 days of temperatures ca. 7 °C above ambient had a permanent negative effect on oil concentration at final harvest, particularly when the exposure to high temperature took place at the beginning of oil accumulation. By contrast, oleic acid concentration at the end of the treatment interval fell with increasing temperature but it could recover after treatment was removed in all periods except the first one. These results show that high temperatures during the oil accumulation phase may negatively affect olive oil yield and quality in warm regions, particularly if the high-temperature event occurs early in the phase. Additionally, the response of oleic acid concentration (%) to temperature under our experimental conditions was found to be opposite to that of many annual oil-seed crops.     

Effect of fruit load on oil yield components and dynamics of fruit growth and oil accumulation in olive (Olea europaea L.)

Olive oil yield and its components (fruit number, average fruit weight and fruit oil concentration) depend on crop load and source–sink ratios as affected by environmental conditions, management and the alternate bearing typical of the species. The aims of this work were to: (i) establish quantitative relationships between oil yield and its components as affected by fruit load in a high-yielding production system, (ii) analyse the dynamics of fruit weight and fruit oil concentration in terms of rates and durations, and (iii) explore the relationships between the dynamics of oil and water in fruit. In a fully irrigated olive orchard in Mendoza (32° S), Argentina, cv. Arbequina trees with similar crown volume and three fruit loads (3-fold range) were monitored during two seasons. Oil yield was positively associated with both fruit number and fruit fresh weight, but not with fruit oil concentration. Across seasons and fruit loads, fruit yield increased linearly with fruit number at ～1.5 kg per thousand fruit and reached a maximum ～60 kg tree^?1 (or 25 t ha^?1) at a fruit load of 32,700 fruit tree^?1. The fruit filling rate was affected by fruit load, while the duration of fruit growth and the dynamics of oil and water concentration were unaffected by fruit load. Fruit water concentration reached a minimum at the onset of Stage III of fruit growth, which was marked by a rapid increase in oil concentration. Fruit fresh weight and oil weight increased with source–sink ratio from ～0.5 up to a threshold ～2 m³ crown per thousand fruit. In contrast, a 8-fold range of source–sink ratio did not affect fruit oil concentration.     

Opposite oleic acid responses to temperature in oils from the seed and mesocarp of the olive fruit

Olive oil is mostly extracted from the mesocarp (∼95%) of the fruit with the seed (endosperm and embryo, ∼5%) containing little oil. There are correlative and manipulative evidence that temperature modulates fruit oil content and fatty acid composition of the oil from the whole fruit (i.e., with no distinction being made between oils derived from each oil-bearing structure) of olive. Notably, oleic acid concentration of olive oil decreases as fruit mean growth temperature increases. This response in the olive fruit is opposite to that documented in annual oil-seed crops such as sunflower and soybean. The objectives of the present study were: i) to compare temperature effects on fatty acid composition of oil derived from seed and from mesocarp; ii) to compare temperature effects on seed and mesocarp dry weights and oil concentrations. To do this, fruiting branches were enclosed in transparent plastic chambers with individualized temperature control. Temperature was manipulated during the seed growth (Period A) and during the second half of mesocarp growth (Period B) subphases. In both periods, the oleic acid proportion in mesocarp oil decreased as temperature increased, and was accompanied by increases of palmitic acid, linoleic and linolenic acids. Mesocarp dry weight did not respond significantly to temperature, but mesocarp oil concentration fell significantly as temperature increased. Seed dry weight, oil concentration and fatty acid composition exhibited responses to temperature during Period A only, with seed dry weight increasing between 20 and 25 °C with a sharp decrease at higher temperature, and oil concentration linearly falling 1.2% per °C. In contrast, seed oil oleic acid percentage increased between 20 and 28 °C, and fell slightly with higher temperature. Palmitic and stearic acids in seed oil increased sigmoidally with temperature, while linoleic acid decreased sigmoidally. Oleic acid percentage showed opposite responses in oil from the seed and the mesocarp. The response of the seed to temperature was similar to those observed in oil from embryos of annual oil-seed crops, although the abrupt fall in palmitic and stearic acid with temperature >25 °C seems to be distinctive for olive seed oil.     

A dynamic model of potential growth of olive (Olea europaea L.) orchards

A model of potential olive oil production is presented, based on a three-dimensional model of canopy photosynthesis and respiration and dynamic distribution of assimilates among organs. The model is used to analyse the effects of planting density (high and super-high density orchards with 408 and 1667 trees ha⁻¹, respectively) and climate change (ΔT of 4 °C and CO₂ concentration of 740 ppm) on olive oil production. To evaluate its predictive power, the simulations were tested with published measurements of leaf area, growth and yield for a high density olive orchard cv. ‘Arbequina’ in Cordoba, Spain. The model slightly overestimated (less than 7%) the different measurements reported in the experiment. For all simulations, the maximum yields obtained were in agreement with literature. Simulations showed that climate change had a very small effect on yields due to compensation of the negative and positive effects of temperature and CO₂ on photosynthesis and respiration. However, high temperatures led to some sterile years due to lack of vernalization. The model predicts that super-high density olive orchards achieve higher potential yields than high-density systems and that maximum yields are reached on the third year of the orchard. The advantage of a higher density is a higher interception of solar radiation, especially during the first years of the orchard. In all the simulations, the model predicted a small decrease of the radiation use efficiency for oil production with the age of the orchard as well as an important inter-annual variability (range of 0.11–0.19 g (MJ PAR)⁻¹), indicating that the use of a constant radiation use efficiency may not be adequate to predict oil production.     

Effect of cold storage on vitamin C,phenolics and antioxidant activity of five orange genotypes [Citrus sinensis (L.) Osbeck]

The effect of cold storage on antioxidant profile and the antioxidant activity of five sweet orange genotypes [Citrus sinensis (L.) Osbeck], three blood (pigmented) varieties with different anthocyanin contents (‘Tarocco Messina’, ‘Tarocco Meli’ and ‘Moro’) and two blond varieties (‘Ovale’ and ‘Valencia late’), stored at 6 ± 1 °C for 65 d was investigated. During fruit storage, anthocyanins, hydroxycinnamic acids, vitamin C, flavanones and total phenolics were determined, and juice antioxidant capacity was measured by two different in vitro tests (DPPH scavenging activity and inhibition of induced linoleic acid peroxidation). The results showed an increase in anthocyanins, flavanones and hydroxycinnamic acids and a slight decrease in vitamin C in the blood oranges. Cold storage negatively affected flavanone concentration, while positively influenced vitamin C in blond orange varieties. Both antioxidant activity tests showed an increase in antioxidant capacity during storage caused mainly by phenolic accumulation (blood oranges) and vitamin C increase (blond oranges). Finally, correlations between antioxidant activity and total or individual phenolic components were examined.     

The addition of rosehip oil improves the beneficial effect of Aloe vera gel on delaying ripening and maintaining postharvest quality of several stonefruit

In this work Aloe vera gel (AV) alone or with the addition of 10 or 2% rosehip oil was used as fruit edible coatings in a wide range of Prunus species and cultivars: peaches (‘Roma’ and ‘B-424-16’ flat type), plums (‘Red Beauty’ and ‘Songria’), nectarine (‘Garofa’) and sweet cherry (‘Brooks’). Following treatments, fruit were stored at 20 °C for 6 days and analysed for the effect of treatments on fruit ripening and quality parameters compared with uncoated fruit (control). The addition of the rosehip oil to AV gel reduced respiration rate in all fruit, and ethylene production in the climacteric ones (peaches, plums and nectarine). In addition, all the parameters related with fruit ripening and quality, such as weight loss, softening, colour change and ripening index, were also delayed in treated compared with control fruit, the effect being generally higher when rosehip oil was added to AV, and especially in those fruit that exhibited the highest ethylene production rates (‘Roma’ and flat type peaches). Although the highest effect was obtained with AV + rosehip oil at 10%, the sensory panel detected an excess of gloss and oiliness on the fruit surface, which was considered as a negative attribute. Thus, 2% rosehip oil added to AV could be used as an innovative postharvest tool to increase the beneficial effect of AV as an edible coating, especially in climacteric fruit showing high ethylene production rates.     

Essential oil vapours suppress the development of anthracnose and enhance defence related and antioxidant enzyme activities in avocado fruit

Anthracnose caused by Colletotrichum gloeosporioides is a major postharvest disease in avocados that causes significant losses during transportation and storage. Complete inhibition of the radial mycelia growth of C. gloeosporioides in vitro was observed with citronella or peppermint oils at 8 μL plate⁻¹ and thyme oil at 5 μL plate⁻¹. Thyme oil at 66.7 μL L⁻¹ significantly reduced anthracnose from 100% (untreated control) to 8.3% after 4 days, and to 13.9% after 6 days in artificially wounded and inoculated ‘Fuerte’ and ‘Hass’ fruit with C. gloeosporioides. GC/MS analysis revealed thymol (53.19% RA), menthol (41.62% RA) and citronellal (23.54% RA) as the dominant compounds in thyme, peppermint and citronella oils respectively. The activities of defence enzymes including chitinase, 1, 3-β-glucanase, phenylalanine ammonia-lyase and peroxidase were enhanced by thyme oil (66.7 μL L⁻¹) treatment and the level of total phenolics in thyme oil treated fruit was higher than that in untreated (control) fruit. In addition, the thyme oil (66.7 μL L⁻¹) treatment enhanced the antioxidant enzymes such as superoxide dismutase and catalase. These observations suggest that the effects of thyme oil on anthracnose in the avocado fruit are due to the elicitation of biochemical defence responses in the fruit and inducing the activities of antioxidant enzymes. Thus postharvest thyme oil treatment has positive effects on reducing anthracnose in avocados.     

Table olive cultivar susceptibility to impact bruising

Developing mechanical harvesting for table olives will require decreasing fruit damage during harvest and postharvest handling, transport and storage. The susceptibility to bruising and its development over time were studied in three table olive varieties, cv. ‘Manzanilla’, ‘Gordal Sevillana’ and ‘Hojiblanca’. Bruising was produced with controlled energy impacts of 56, 26, 13 mJ. A strong correlation (r² = 0.77–0.90) between bruise volume and impact energy was demonstrated. Bruise susceptibility was higher in the Manzanilla variety, followed by Hojiblanca and Gordal Sevillana cultivars. Bruise time evolution was evaluated using a spectrophotometer for visible and near infrared regions. A bruise index was developed using different wavelengths, 545, 670 and 800 nm. Most darkening due to the browning process happened within 1 h, was exponential and dependent on impact energy level. The discoloration was greatest in the Manzanilla, followed by Hojiblanca and Gordal Sevillana olives.     

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.     

Storage temperature and time influences sensory quality of mandarins by altering soluble solids,acidity and aroma volatile composition

Mandarins are very prone to losing flavor quality during storage and, as a result, often have a short shelf life. To better understand the basis of this flavor loss, two mandarin varieties (‘W. Murcott’ and ‘Owari’) were stored for 0, 3 and 6 weeks at either 0 °C, 4 °C, or 8 °C plus 1 week at 20 °C, and then evaluated for sensory attributes as well as quality parameters and aroma volatile profile. The experiment was conducted multiple times for each variety over two seasons, using three separate grower lots per experiment. Flavor quality was reduced in ‘Owari’ following 4 weeks of storage as off-flavor increased, while for ‘W. Murcott’ the hedonic score decreased after the fruit were stored for 7 weeks. Sensory panelists also noted a decline in tartness during storage for both varieties that was associated with an increase in the ratio of soluble solids concentration (SSC) to titratable acidity (TA). Large increases in alcohols and esters occurred during storage in both varieties, a number of which were present in concentrations in excess of their odor threshold values and are likely contributing to the loss in flavor quality. Thirteen aroma volatiles, consisting mainly of terpenes and aldehydes, declined during storage by up to 73% in ‘Owari’, only one of which significantly changed in ‘W. Murcott’. Although many of these volatiles had aromas characteristic of citrus, their involvement in flavor loss during storage is unclear. ‘W. Murcott’ stored at 8 °C had slightly superior flavor to fruit stored at either 0 °C or 4 °C, and the better flavor was associated with higher SSC/TA and lesser tartness. Aroma volatiles did not play a role in the temperature effect on flavor as there were no significant differences in volatile concentrations among the three temperatures. There was no effect of storage temperature on the flavor of ‘Owari’.     

Cultivar differences in gaseous 1-methylcyclopropene accumulation in whole and fresh-cut apple fruit

A number of studies have shown that responses of apple fruit to 1-methylcyclopropene (1-MCP) vary considerably among cultivars. This study was designed to determine if cultivars show differences in accumulation of gaseous 1-MCP. Apple fruit were placed in 1.76 L jars that were sealed and injected with 20 μL L⁻¹ 1-MCP. After 12 h, samples of intercellular atmosphere were removed and analyzed for 1-MCP concentration. Accumulation of internal gaseous 1-MCP varied markedly among cultivars, ranging from 0.14 ± 0.06, 0.22 ± 0.03, and 0.77 ± 0.30 in ‘Redcort’, ‘McIntosh’, and ‘Empire’, respectively, to 2.10 ± 0.28, 3.33 ± 0.13, and 6.93 ± 0.35 μL L⁻¹ in ‘Gala’, ‘Cameo’, and ‘Honeycrisp’, respectively. Accumulation of gaseous 1-MCP was reduced an average of 51% in fruit treated with Sta-Fresh 8711 fruit wax. The role of the epidermis in modulating 1-MCP ingress was determined by measuring gaseous 1-MCP accumulation in fresh-cut tissue. Fresh-cut cortical tissue rapidly depleted headspace 1-MCP (>95%) over a 1-h exposure yet accumulated negligible quantities of internal gaseous 1-MCP. By contrast, cortical tissue treated with ascorbic acid or hypotaurine, or aged for several hours prior to exposure to 1-MCP, showed reduced consumption of headspace 1-MCP and high accumulation of internal gaseous 1-MCP. Levels of internal 1-MCP in cortical tissue from the cultivars generally paralleled those for intact fruit, ranging from 0.23 ± 0.07, 0.37 ± 0.18 and 1.09 ± 0.14 μL L⁻¹ in ‘Empire’, ‘McIntosh’ and ‘Redcort’, respectively, to 2.40 ± 0.71, 4.55 ± 0.15, and 6.24 ± 0.85 in Gala’, ‘Cameo’, and ‘Honeycrisp’, respectively. Although commercial fruit wax influences gaseous 1-MCP accumulation, the comparable accumulation patterns in unwaxed whole and fresh-cut apple fruit suggest that epidermal tissue/native waxes alone do not account for cultivar differences.     

Application of optical coherence tomography to non-destructively characterise rind breakdown disorder of ‘Nules Clementine’ mandarins

The feasibility of optical coherence tomography (OCT) for imaging histological changes associated with the development of a progressive rind breakdown (RBD) disorder of ‘Nules Clementine’ mandarin (Citrus reticulate Blanco.) was investigated. The investigation utilised fruit with different levels of the disorder, carefully selected from a batch of fruit stored for eight weeks at 8 ± 0.5 °C. Images of healthy and RBD-affected intact mandarin fruit were acquired using a Thorlabs OCT system based on a broadband 930 nm source. OCT provided high resolution 2D images of fruit rind to a depth of about 1.1 mm. Immediate and non-destructive acquisition of images showing histological and microstructural features in intact rind tissues was demonstrated. The oil glands stayed intact in unaffected fruit and gradually collapsed in RBD affected fruit. At advanced stages of the disorder, the collapsed oil glands became increasingly deformed and flattened. The study showed that OCT is a promising technique for immediate, real-time and non-destructive acquisition of images showing histological and microstructural rind features of ‘Nules Clementine’ mandarin fruit.     

Volatile profiles of ripening West Indian and Guatemalan-West Indian avocado cultivars as affected by aqueous 1-methylcyclopropene

Separate experiments were conducted with three major commercial avocado (Persea americana Mill.) cultivars grown in Florida: ‘Simmonds’ (early-season, West Indian race); ‘Booth 7’ (mid-season, Guatemalan-West Indian hybrid); and ‘Monroe’ (late-season, Guatemalan-West Indian hybrid). Fruit were harvested at preclimacteric stage and left untreated (Control) or treated 24 h after harvest with aqueous 1-methylcyclopropene (1-MCP) at 1.39 (treatment M1) or 2.77 μmol L⁻¹ a.i. (treatment M2) (75 or 150 μg L⁻¹) for 1 min at 20 °C. Whole fruit ripening was monitored at 20 °C/92% ± 3% R.H. and based on whole fruit firmness, respiration and ethylene evolution. Fruit volatiles were assessed at preclimacteric (24 h after harvest), mid-ripe (half of initial fruit firmness) and ripe maturity stages, from 100 g of chopped pulp using a purge and trap system. Untreated, firmer fruit ‘Monroe’ (268 N at harvest) ripened within 12 d of harvest while softer fruit ‘Simmonds’ (118 N) ripened within only 6 d. 1-MCP treatment extended ripening time from 33% (M1) to 83% (M2). All fruit softened normally, indicating the potential benefits of aqueous 1-MCP as a postharvest treatment for avocado when applied at these concentrations. Volatile profiles differed among the three cultivars with several compounds detected in only one cultivar, results that may contribute to a potential identification of the origin of the cultivar based on fruit volatile composition. The West Indian cultivar ‘Simmonds’ had much higher emission of hexanal (preclimacteric fruit) and cis-3-hexenal and cis-3-hexen-1-ol (ripe fruit) than the Guatemalan-West Indian hybrids ‘Booth 7’ and ‘Monroe’. On the other hand, these latter hybrids had much higher levels of alkanes than ‘Simmonds’. Treatment with 1-MCP increased emissions of alkanes during ripening of ‘Booth 7’ and ‘Monroe’. Total volatiles of avocado decreased during ripening mainly due to the significant reduction of sesquiterpenes, the main group of volatiles in all cultivars at harvest (‘Simmonds’, 53%; ‘Booth 7’, 78%; ‘Monroe’, 66%). β-Caryophyllene was the major compound at harvest, but decreased to less than 2% in ripe fruit, at which point most sesquiterpenes were not detected. Among the 10 sesquiterpenes commonly found in the avocado cultivars in this study, only α-Copaene had significantly higher emissions in mid-ripe fruit treated with the higher concentration of 1-MCP (2.77 μmol L⁻¹ a.i.), suggesting that ethylene participates in the regulation of this sesquiterpene.     

Effect of gamma irradiation on the physico-chemical and visual properties of mango (Mangifera indica L.), cv. ‘Dushehri’ and ‘Fazli’ stored at 20 °C

The effect of γ-irradiation doses (0.3, 0.5, 0.7, 1.0, 6.0, 10.0 kGy) on different physico-chemical and visual properties of two Indian cultivars of mango, cv. ‘Dushehri’ and ‘Fazli’ was observed during storage at 20 °C for the evaluation of delayed ripening and extension of shelf-life. Visually all the irradiated fruit showed greener peel and lighter pulp throughout the storage, however, radiation injuries were present in ‘Dushehri’ treated with 6–10 kGy and in ‘Fazli’ with 1–10 kGy. Loss of fruit due to rotting was less in the irradiated samples, treated up to 1 kGy of both the cultivars. Irradiated fruit of both the cultivars at high doses (6–10 kGy) showed increased sugar content from 0 d, however, all the treated fruit registered a slower rate of increase of sugars with storage compared to the respective controls and those treated with the lower doses of 0.5 and 0.7 kGy attained peak sugar concentration later. Significant (p ≤ 0.05) textural deterioration could be detected immediately after irradiation, in ‘Dushehri’ at doses ≥1 kGy and in ‘Fazli’ at doses ≥0.7 kGy. However, low dose treated fruit (0.3–1 kGy) of both the cultivars softened at a considerably slower rate during storage and registered significantly greater fruit firmness (compression strength) throughout the storage period. Similarly, ‘Dushehri’ treated with 0.3–0.7 kGy and Fazli treated with 0.7 kGy registered significantly greater flesh firmness (shear strength). ‘Dushehri’ treated with 0.3–1 kGy and ‘Fazli’ with 0.5–1 kGy also registered significantly harder and tougher peel, as determined by puncture test, throughout the storage. Scanning electron microscopy (SEM) performed on 3rd and 2nd d of storage of ‘Dushehri’ and ‘Fazli’ respectively, revealed microstructural breakdown at and above 1 kGy in both cultivars. Cell separation could be observed in ‘Fazli’ even at 0.7 kGy. SEM also revealed that the control fruit were in a more advanced stage of ripening than the low dose treated fruit. The study showed the feasibility of low dose γ-irradiation on ‘Dushehri’ (0.3–0.7 kGy) and ‘Fazli’ (0.5 and 0.7 kGy) that induced useful delay in ripening and extension of shelf-life by a minimum of 3 and 4 d, respectively.     

Modeling the effect of preharvest weather conditions on the incidence of soft scald in ‘Honeycrisp’ apples

‘Honeycrisp’ apples show a high susceptibility to physiological disorders such as soft scald. The objective of this study was to identify weather parameters during fruit development that influence soft scald development in ‘Honeycrisp’ apples. Soft scald susceptibility of ‘Honeycrisp’ has been linked to weather conditions during specific periods of the growing season, referenced by given phenological stages. Using weather data and fruit quality analysis data from three sites in Ontario, two sites in Quebec and one site in Nova Scotia for three seasons (2009–2011) and four additional sites in Ontario from 2002–2006, a model for soft scald incidence (SSI) was built to predict the susceptibility of ‘Honeycrisp’ apples prior to storage. This model used primarily two weather variables during three sub-periods of fruit development to accumulate a SSI index (%) during the growing season, from full bloom to harvest time. Relatively wet conditions during phenological stages from full bloom until 10 mm diameter (precipitation > 0.5 mm) and from 10 mm until 50% of final caliber (precipitation > 6.0 mm), cool conditions (temperature < 15 °C) from full bloom until 10 mm diameter, and warm conditions (temperature > 20 °C) from 50 to 80% of final size are conditions that resulted in increased soft scald susceptibility for ‘Honeycrisp’ apples. The SSI model may be used by producers to establish more appropriate marketing and storage strategies depending on levels of susceptibility to soft scald development predicted prior to storage.     

Efficacy of 1-MCP treatment in tomato fruit: 2. Effect of cultivar and ripening stage at harvest

Four cultivars of tomato fruit (‘Cherry’, ‘Daniela’, ‘Patrona’ and ‘Raf’) were harvested at two ripening stages (S1 and S2), treated with 0.5 μl l⁻¹ of 1-methylcyclopropene (1-MCP) for 24 h and stored at 10 °C for 28 days. For all cultivars, control fruit deteriorated very rapidly (due to weight loss, softening, colour changes and decay) with an estimated shelf life of 7 days (‘Cherry’ and ‘Patrona’) and 14 days (‘Daniela’ and ‘Raf’), independently of the ripening stage at harvest. All quality parameters for all cultivars were delayed and/or inhibited in treated fruit, the efficacy of 1-MCP being higher in tomatoes harvested at the S2 ripening stage. At this stage, the organoleptic properties had already developed in fruit on the plant and tomatoes could thus reach consumers with optimal postharvest quality.     

Increasing the rate of ripening of date palm fruit (Phoenix dactylifera L.) cv. Helali by preharvest and postharvest treatments

‘Helali’ is a late season date palm cultivar. At the mature (Bisir) stage, the fruit are astringent as a result of high contents of soluble tannins, and removal of tannins is necessary for the fruit to be edible. During the harvesting season, only 30–40% of the total fruit might normally ripen (Rutab stage) on the tree and the remaining fruit fail to ripen. This study showed that bunch bagging with different materials such as black or blue polyethylene bags, white ‘agrlsafe’ (polypropylene fleece) and paper bags during the growing season significantly increased the rate of fruit ripening and increased Rutab yield per bunch. In this respect, black and blue polyethylene bags were the most effective followed by ‘agrlsafe’ and paper bags. Preharvest ethrel application significantly increased Rutab fruit yield per bunch compared to the controls. There were no significant differences in Rutab yield per bunch between sprays or injection of ethrel into the bunch peduncle. Postharvest dipping of fruit at the Bisir stage in ethrel at 4.2 ml/l and abscisic acid at 1.0 mM significantly enhanced ripening, compared to the controls. However, ABG-3168 (an ethylene blocker) application at 3.33 g/l significantly inhibited ripening, suggesting a role for ethylene in the ripening process. Ethanol vapor significantly hastened ripening of Bisir fruit over 10 days at ambient conditions in desiccators. The response of immature fruit (according to fruit density and TSS) to ethanol vapor was much greater than mature ones. Also, immersion of fruit in water for 10 h significantly increased fruit ripening compared to the controls, but to a lesser extent. It is concluded that ‘Helali’ date ripening could be hastened by bunch bagging during growth, or by exposing the Bisir fruit to ethanol vapor following harvest. Neither treatment showed any negative impact on the overall quality characteristics of ripe fruit, suggesting that they may be practical tools for increasing the ripening rate of Bisir ‘Helali’ dates.     

Degreening behavior in ‘Fallglo’ and ‘Lee × Orlando’ is correlated with differential expression of ethylene signaling and biosynthesis genes

Two citrus types (‘Fallglo’ and ‘Lee × Orlando’) exhibiting differential fruit degreening response when treated with ethylene were selected. Fruit were harvested at commercial maturity but at different developmental periods (Harvest I, II and III). Rate of color change was greater in ‘Fallglo’ than in ‘Lee × Orlando’ when fruit were treated with 5 μL L⁻¹ of ethylene for 24 h. After 24 h of transfer of fruit to ethylene-free storage, rate of change decreased in ‘Fallgo’ and exhibited varied response in ‘Lee × Orlando’ depending on harvest date. ‘Fallglo’ fruit from Harvests I and II were completely degreened at the end of storage for 7 d; however ‘Lee × Orlando’ were not and were green in color. No difference in seedling triple response was observed between ‘Fallglo’ and ‘Lee × Orlando’ and sequences of the four ethylene receptors were identical between them. Expression of genes involved in ethylene biosynthesis and signaling pathways were studied in flavedo to test if differences in these pathways were correlated with differential ethylene sensitivity of the citrus types. Basal levels of ACS2 and ACO expressions declined as maturity progressed, and ethylene-induced expression of ACS1 and ACO were influenced by fruit maturity. At Harvests I and II, ethylene-induced increase in ACS1 and ACO expressions and ACC levels were greater in ‘Fallglo’ than in ‘Lee × Orlando’. Ethylene treatment influenced MACC content only during Harvest I in ‘Lee × Orlando’. MACC levels were generally higher in ‘Lee × Orlando’ than in ‘Fallglo’. Expressions of ETR1 and ETR2 were ethylene responsive in ‘Fallglo’ and only ETR1 expression was ethylene responsive in ‘Lee × Orlando’. Ethylene had more impact on ETR1 expression in ‘Fallglo’ than in ‘Lee × Orlando’. Ethylene had a negative effect on ETR3 expression which was more pronounced in ‘Lee × Orlando’ than in ‘Fallglo’. Expressions of ERS1, CTR1, EIN2, EIL1 and EIL2 were not affected by ethylene in both citrus types. Expression of chlorophyllase gene and rate of total chlorophyll degradation were higher in ‘Fallglo’ than in ‘Lee × Orlando’ during ethylene treatment. Differential degreening behavior of ‘Fallglo’ and ‘Lee × Orlando’ correlated with peel maturity, and factor(s) downstream of ethylene signaling but upstream of ethylene biosynthesis play a role in the differential sensitivity.     

Responses of 1-MCP application in plums stored under air and controlled atmospheres

The potential of 1-MCP for controlling ripening in ‘Angeleno’ plum fruit under air and controlled atmosphere (CA) storage was explored, and the possibility that 1-MCP can inhibit development of brown rot caused by Monilinia laxa and internal breakdown in ‘Fortune’ and ‘Angeleno’ plums tested. After harvest, fruit were exposed to 300 and 500 nl l⁻¹ (in 2003) and 500 nl l⁻¹ 1-MCP (in 2004) at low temperatures (0–3 °C) for 24 h. After treatment the plums were stored in air at 0 °C and ‘Angeleno’ fruit were also stored in CA storage (1.8% O₂ + 2.5% CO₂). Following storage, fruit were kept at 20 °C. In ‘Angeleno’ fruit, 1-MCP was effective in delaying the loss of firmness and colour changes during holding at 20 °C. 1-MCP reduced brown rot in fruit stored in CA but no significant reduction was found in air storage. Internal breakdown, a major physiological storage disorder in plums, was inhibited by 1-MCP treatment. Furthermore, since 1-MCP applied in air storage showed better results than the control in CA conditions, an application of 1-MCP before air storage could be the best way to reduce the ripening process for short or medium storage periods (40 and 60 days). CA storage plus 1-MCP treatment could be used for long periods (80 days).