Internal browning disorder and fruit quality in modified atmosphere packaged ‘Bartlett’ pears during storage and transit

Internal browning (IB) can be a serious problem with the use of modified atmosphere packaging (MAP) for ‘Bartlett’ pears (Pyrus communis L.) grown in the Pacific Northwest during storage and transit to distant markets. To investigate this disorder, ‘Bartlett’ pears harvested at commercial maturity were packed in a commercial MAP (MAPc), an experimental MAP (MAPe) and commercial perforated plastic bags (control) and stored in air at −1.1 °C. After 1 and 3 months of storage, samples of MAPc and control fruit were transferred to rooms at temperatures of 2, 4.5, 7.5, and 10 °C for 3 weeks to simulate transit temperatures and the time required to reach distant markets. MAPc maintained an average internal atmosphere of 12.3% O₂ + 5.6% CO₂ and significantly extended ‘Bartlett’ pear storage life with high eating quality and without IB and other disorders for up to 4 months at −1.1 °C. The internal gas atmosphere of MAPe equilibrated at 2.2% O₂ + 5.7% CO₂, which resulted in fruit with 25.5 and 62.3% IB after 3 and 4 months of storage, respectively. During simulated transit conditions of 2, 4.5, 7.5, and 10 °C, the CO₂ level in MAPc was maintained at 5.6–7.9%, while O₂ was reduced dramatically to 10.5, 5.0, 2.5, and 1.0%, respectively. IB developed at 7.5 and 10 °C but not at 2 and 4.5 °C, regardless of pre-transit storage duration (1 and 3 months) at −1.1 °C. The longer the storage duration and the higher transit temperature, the higher the incidence and severity of IB. The MAP-related IB disorder observed in this study included two types of symptoms: classic pithy brown core and wet brown flesh. The MAPc storage gas atmospheres maintained fruit firmness, color and higher eating quality after ripening, eliminated senescent scald and core breakdown, suppressed the loss of ascorbic acid (AsA) and titratable acidity, and slowed the accumulation of malondialdehyde (MDA) during storage at −1.1 °C for up to 4 months or 3 months + 3 weeks at simulated transit temperatures of 2 and 4.5 °C. In contrast, fruit held in MAP with low O₂ levels (1.0–2.5%) developed IB that appeared to be associated with a reduction in AsA, accumulated MDA and exhibited an increase in membrane leakage. MAP inhibited ripening at high CO₂ + high O₂ but lead to IB when the packaging material or elevated temperatures resulted in high CO₂ + low O₂ conditions. The incidence of IB closely correlated with lipid peroxidation and appeared to be related to fruit AsA concentration. The MAPc designed for pears appears to be suitable for ‘Bartlett’ fruit stored at −1.1 °C for up to 4 months or storage for 3 months and a transportation duration of up to 3 weeks at 0–4.5 °C during the early season and at 0–2 °C during the late packing season. These conditions yielded fruit of high eating quality and without IB or over-ripening upon arrival at distant markets.     

Ripening behavior and quality of modified atmosphere packed ‘Doyenne du Comice’ pears during cold storage and simulated transit

The effect of MAP on extending storage life and maintaining fruit quality was studied in ‘Doyenne du Comice’ (Pyrus communis L.) pears at Hood River and Medford, Oregon. Control fruit packed in standard perforated polyethylene liners started to show senescent core breakdown and lost the capacity to ripen at 20 °C after 4–5 months of cold storage in Hood River and after 5.25–6 months in Medford. LifeSpan^® L257 MAP achieved steady-state atmospheres of 15.8% O₂ + 3.7% CO₂ in Hood River and 15.7–17.5% O₂ + 3.8–5.7% CO₂ in Medford. MAP inhibited ethylene production, ascorbic acid degradation and malondialdehyde accumulation, and extended storage life for up to 6 months with maintenance of fruit flesh firmness (FF) and skin color without commercially unacceptable level of physiological disorders. After 4, 5 and 6 months at −1 °C, MAP fruit exhibited climacteric-like patterns of ethylene production and softened to proper texture with desirable eating quality on day 5 during ripening at 20 °C. After 6 months at −1 °C plus 2 weeks of simulated transit conditions, MAP fruit maintained FF and skin color and had good eating quality at transit temperatures of 2 and 4.5 °C (10.1–11.5% O₂ + 4.8–5.2% CO₂), but reduced FF substantially and developed internal browning disorder at 7.5 and 20 °C (3.2–7.2% O₂ + 7.9–9.5% CO₂). The storage life of ‘Doyenne du Comice’ pears with high eating quality could be increased by up to 2 months when packed in MAP as compared with fruit packed in standard perforated polyethylene liners.     

Dynamics of ascorbic acid in ‘Braeburn’ and ‘Gala’ apples during on-tree development and storage in atmospheres conducive to internal browning development

The underlying causes as well as chemical and biochemical alleviation for CO₂-induced browning in apple fruit are poorly understood. Ascorbic acid (AsA) dynamics in ‘Braeburn,’ a susceptible cultivar, and ‘Gala’, a resistant cultivar, were evaluated during on-tree development and storage at 0.5 °C in air or controlled atmospheres (CA) containing 1 kPa O₂ and 1, 3 or 5 kPa CO₂. ‘Braeburn’ fruit treated with diphenylamine (DPA) was also stored for 1 month to determine effects on browning incidence and AsA concentration. ‘Braeburn’ apples had significantly higher (p ≤ 0.05) AsA levels than ‘Gala’ during on-tree development, and storage. No correlation between AsA and maturity/ripening indices for ‘Braeburn’ or ‘Gala’ was apparent. Histochemical localization of fruit AsA showed a staining intensity consistent with the quantity analytically determined, and showed that AsA is diffusely distributed throughout the cortex in both cultivars during on-tree development. During storage, AsA was localized to the periphery of brown tissue in ‘Braeburn’ and to the coreline and cortex proximal to the peel in ‘Braeburn’ and ‘Gala’ tissues. DPA decreased browning development during storage, however, no correlation between DPA treatment and AsA quantity in healthy or brown cortex tissue was observed. The results indicate AsA quantity alone is not an indicator of CO₂ sensitivity in these two cultivars.     

Effects of cold storage and shelf-life on sensory quality and consumer acceptance of ‘Abate Fetel’ pears

Fruit products certified by quality labels should guarantee high levels of consumer acceptance, despite the unavoidable variability arising from growing conditions and postharvest responses. The quality of ‘Abate Fetel’ pear (Pyrus communis L.) fruit was studied, after short or long cold storage, by analysis of physicochemical, texture and flavour traits, to investigate factors affecting consumer acceptance. Fruit from three orchards differing in location and design, monitored during 10 d of ripening at 20 °C, softened progressively to reach and exceed firmness adequate for consumption. Change in colour, in particular hue angle, paralleled softening. Sensory traits were investigated by evaluating fruit of three different firmness levels within the range of acceptable eating quality. Firmness differences were clearly perceived both by expert judges and by consumers, but did not influence the degree of liking. ‘Abate Fetel’ pear can maintain acceptable eating quality at 20 °C for 4–8 d after 13 weeks storage at ?1 °C, or 2–6 d after 23 weeks storage at ?1 °C. Changing texture parameters were perceived at eating, without compromising overall quality. Production system affected intrinsic quality parameters such as total soluble solids concentration, but did not influence consumer acceptance. In consumer tests conducted after 13 weeks of cold storage, high scores were recorded, with a 86% acceptance frequency and more than 40% of scores reflecting “like very much” or “like extremely”. After 23 weeks of cold storage a decrease in degree of liking was observed. The overall value of ‘Abate Fetel IGP Emilia-Romagna’ quality label was confirmed by consumer evaluations. However, the decrease in consumer acceptance after 23 weeks of cold storage indicates that caution should be used in using long storage durations.     

Canopy position affects rind biochemical profile of ‘Nules Clementine’ mandarin fruit during postharvest storage

This study was conducted to investigate the effects of preharvest canopy position and bagging treatments on rind physiological and biochemical properties of ‘Nules Clementine’ mandarin (Citrus reticulata Blanco) fruit. Before storage, the respiration rate of unbagged outside fruit was significantly higher (21.6 mL CO₂ kg⁻¹ h⁻¹) than of bagged inside fruit (16.3 mL CO₂ kg⁻¹ h⁻¹). Unbagged fruit outside the canopy had 1.4-fold higher carbohydrates, and 1.1-fold higher dry matter (DM) content than bagged inside fruit. Bagged fruit inside the canopy had higher (24%) weight loss than outside sun-exposed fruit (14%). This corresponded with a higher rind breakdown (RBD) index for bagged inside fruit, compared to sun-exposed fruit which did not develop the disorder. During postharvest storage, rind fructose levels of bagged fruit inside the canopy increased from 62.4 mg/g DM at harvest to 81.3 mg/g DM after 8 weeks, while those of unbagged outside fruit increased from 97.9 to 108.4 mg/g DM. Concomitant with the increase in fructose, sucrose in rind tissue of bagged inside fruit decreased from 42.6 to 27.7 mg/g DM and from 49.3 to 33.4 mg/g DM for unbagged outside fruit. Rind glucose of unbagged inside fruit decreased from 90.6 to 76.2 mg/g DM. Ascorbic acid concentrations remained almost constant during storage, with levels between 3.3 and 6.7 mg/g DM for inside bagged and unbagged outside fruit, respectively. Hesperidin was the major flavanone detected, with concentrations between 35 and 45 mg/g DM followed by narirutin (1.1–2.8 mg/g DM). At harvest, rind of fruit harvested from outside the canopy had lower hesperidin concentration (38.1 mg/g DM) compared to shaded fruit (44.2 mg/g DM). Overall, the results suggest that variations in microclimatic conditions inside the tree canopy during the growing season affect the biochemical profile of the fruit rind, which in turn influences fruit response to postharvest stresses associated with senescence and susceptibility to RBD.     

Use of chlorine dioxide fumigation to alleviate enzymatic browning of harvested ‘Daw’ longan pericarp during storage under ambient conditions

Pericarp browning reduces both the shelf-life and market value of harvested longan fruit stored at room temperature. Our study investigated the efficiency of chlorine dioxide (ClO₂) fumigation at reducing pericarp browning of longan (Dimocarpus longan Lour.) cv. Daw. Fresh longan fruit were fumigated with 0 (control), 2.5, 5, 10 and 25 mg/L ClO₂ for 10 min, before being packed in cardboard boxes, and stored at 25 ± 1 °C, RH 82 ± 5% for 7 days. Fruit treated with ClO₂ had a lower browning index, but higher hue angle (true color), L* (lightness) and b* (yellowness) values than non-treated fruit. The 10 and 25 mg/L ClO₂ treatments were the most effective at extending shelf-life from 1 to 5 days, compared with the control, by reducing pericarp browning, the activities of polyphenol oxidase (PPO) and peroxidase (POD), disease development and by maintaining the highest total phenolic content. However, quality acceptance of fruit treated with 10 mg/L ClO₂ was higher than fruits treated with 25 mg/L, as determined by odor and flavor. Consequently, ClO₂ fumigation at a concentration of 10 mg/L was considered to be the most effective treatment to reduce pericarp browning of longan, whilst maintaining fruit quality.     

Targeted metabolomics study of ‘Braeburn’ apples during long-term storage

‘Braeburn’ is an apple cultivar susceptible to the occurrence of internal browning (Braeburn Browning Disorder; BBD) during storage. This physiological disorder is characterized by the development of brown spots inside the fruit, eventually resulting in the formation of cavities. The objective of this study was to investigate the effects of the preharvest application of calcium, potassium and triazole fungicides on the postharvest primary metabolites of ‘Braeburn’ fruit, and to offer a better understanding of the biochemical processes behind internal browning. The primary metabolites of ‘Braeburn’ fruit cortex samples at harvest and after 2 weeks, 4 weeks, 4 months and 8 months of storage at browning-inducing conditions were analyzed using GC–MS. No significant difference in the primary metabolites was observed between the different levels of the applied preharvest applications. Early during storage, fruit developed browning, with the severity increasing with storage duration. This was correlated with a group of primary metabolites that showed either an increase (e.g., alanine, galactose, mannitol, sorbitol, xylose) or a decrease (e.g., malate, sucrose) in concentration with time. Radial distribution of the metabolites in the fruit tissue was also observed; some metabolites (e.g., galactose, mannitol) were higher in concentration in the inner cortex, while the concentrations of other metabolites (e.g., mannose, sucrose) were higher in the outer cortex.     

Effectiveness of 1-MCP treatments on ‘Bartlett’ pears as influenced by the cooling method and the bin material

Wooden bin-stored ‘Bartlett’ pears (Pyrus communis L.) were hydrocooled (HC) or forced-air cooled (FAC) and immediately treated or not with 1-methylcyclopropene (1-MCP) for 24 h. 1-MCP gas concentrations used were 0, 0.3 or 0.6 μL L^?1 (called 0, 0.3 and 0.6, respectively). Fruit were subsequently kept at 20 °C for 20 d or stored at ?0.5 °C and 95% RH for 60, 90, 120 or 150 d. After cold storage, fruit were kept at 20 °C for up to 16 d for further ripening. In another experiment, pears stored in wooden bins (W) or plastic bins (P) were all hydrocooled, treated or not with 0.5 μL L^?1 1-MCP (called 0.5 and 0, respectively), stored at ?0.5 °C and 95% RH for 0, 30, 60, 90 or 120 d, and transferred to 20 °C for further ripening. In FAC pears, increasing 1-MCP concentrations usually resulted in delayed increases in ethylene production and lower ethylene production rates, as well as delayed softening. In contrast, HC-0.3 pear firmness did not differ from that of HC-0 fruit after cold storage. Generally, HC-0.3 pears displayed higher ethylene production and lower firmness values than FAC-0.3 pears after a 7-d exposure to 20 °C, regardless the length of cold storage. FAC-0.6 pears always showed lower ethylene production rates and higher flesh firmness values than HC-0.6 fruit. Soluble solids concentration was not consistently affected by 1-MCP. FAC-0.3 and HC-0.6 fruit showed higher titratable acidity values than HC-0 fruit after 0, 60, 120 and 150 d of cold storage plus 7 d at 20 °C. Effectiveness of 1-MCP treatments on HC pears was influenced by the bin material; P-0.5 pears were firmer than W-0.5 pears after 7 d at 20 °C, regardless the length of the cold storage. HC-0.5 fruit exposed to ?0.5 °C for 90 d reached eating quality (firmness ≤23 N) by day 7 if placed in W, and by day 21 when stored in P. Results and previous evidence suggest that wet wooden bin material may represent a major though unpredictable source of 1-MCP sorption that could bind a significant percentage of the 1-MCP applied. When used at relatively low doses 1-MCP partial removal by wet wooden bins can compromise the application effectiveness for controlling ethylene action.     

Polyphenoloxidase activity and browning in fresh-cut ‘Rocha’ pear as affected by pH,phenolic substrates,and antibrowning additives

The effect of pH, phenolic substrates, and food additives on polyphenoloxidase (PPO) activity and on tissue browning was studied in fresh-cut ‘Rocha’ pear. Substrates 4-methylcatechol, caffeic acid, (+)-catechin hydrate, catechol, chlorogenic acid, dopamine hydrochloride, and pyrogallol, were prepared in citric acid-phosphate buffer at pHs ranging from 3.0 to 8.0. pH optima for PPO activity depended on the phenolic substrate. Activity was optimal at pH 5.0 for catechol and 4-methylcatechol; pH 6.0 for chlorogenic acid; pH 7.0 for dopamine, caffeic acid, and catechin; and pH 8.0 for pyrogallol. Discrepancies were observed between the pH dependency of PPO activity and browning, as assessed by objective color measurement. Significant correlations were obtained between enzyme activity and metric-hue difference (ΔH*) over the pH range 3.0–8.0 for four of the eight phenolics. Chlorogenic acid, the main PPO substrate in ‘Rocha’ pear, induced high tissue browning but very low PPO activity at pH 3.0–4.0. Chemical inhibition of PPO was tested using catechol as substrate, and buffer solutions containing 250 mM Ca²⁺ in four salts (ascorbate, chloride, lactate and propionate), 57 mM ascorbic acid, 61 mM N-acetyl-l-cysteine and 3 mM 4-hexylresorcinol. PPO inhibition by additives was affected by the pH of the buffer, and was more effective with ascorbic acid, N-acetyl-l-cysteine and calcium ascorbate. It was concluded that inferences on tissue browning based on PPO activity can be misleading. Measurement of tissue color is proposed as a reliable means to assess the antibrowning effectiveness of additives and the pH of additives for cut pear should be corrected to reduce the browning potential.     

Effect of initial hermetic sealing on quality of ‘Kyoho’ grapes during storage

Experiments of initial hermetic sealing using high barrier film were carried out on ‘Kyoho’ grapes (Vitis vinifera L. × V. Labrusca L. cv. Kyoho) in the 2008 and 2009 fruit seasons, to investigate their potential to enhance quality and extend storage life of the fruit. In the 2008 season, grapes were packaged in high barrier film bags for 1, 2, 3, 4 and 5 weeks, and a modified atmosphere (MA) of low oxygen and high carbon dioxide was formed after sealing. After packaging, fruit were removed from bags and stored in air for up to 90 d at 0 °C. In the 2009 season, grapes were packaged in perforated bags, or in high barrier film bags for 2 weeks and subsequently perforated bags to avoid further anoxia and excessive CO₂ accumulation. After treatment, fruit were stored for up to 90 d at 0 °C, followed by shelf-life at 20 °C for 7 d. Non-packaging air storage was used as a control in both seasons. Fruit quality attributes including soluble solids, titratable acidity, stem browning, berry drop and decay incidence were measured. The results indicated that short-term initial MAP (≤2 weeks) had potential for improving appearance of bunches and maintaining the quality of berries during long-term storage, and significantly reduced quality deterioration. Stems were greener and berry drop and decay incidence were more effectively controlled when fruit were sealed in high barrier film bags for 2 weeks and the bags were subsequently perforated.     

Integrated ethylene and temperature conditioning for induction of ripening capacity in ‘Anjou’ and ‘Comice’ pears

‘Anjou’ and ‘Comice’ pears from three harvest dates were conditioned to develop ripening capacity by exposure to 100 μL L⁻¹ ethylene at 20 °C for 0, 24, 48, or 72 h, followed by varying durations of temperature conditioning at −0.5 or 10 °C. Ripening capacity was tested by measuring fruit firmness after 7 d at 20 °C after completion of conditioning treatments. Fruit firmness was also measured after conditioning but before ripening, and was designated “shipping firmness”, indicative of the potential for the fruit to withstand transport conditions without physical injury. Ripening capacity in both cultivars developed more rapidly with later harvest date, increasing duration of ethylene conditioning, and increasing duration of temperature conditioning. Ripening capacity developed much more rapidly at 10 °C than at −0.5 °C. Useful durations of temperature conditioning at 10 °C were limited by fruit softening below acceptable values of shipping firmness. However, sequential combinations of ethylene and temperature conditioning at both −0.5 and 10 °C were identified wherein post-conditioning shipping firmness was acceptable.     

Ethylene synthesis,ripening capacity,and superficial scald inhibition in 1-MCP treated ‘d’Anjou’ pears are affected by storage temperature

A continuing challenge for commercializing 1-methylcyclopropene (1-MCP) to extend the storage life and control superficial scald of ‘d’Anjou’ pear (Pyrus communis L.) is how to initiate ripening in 1-MCP treated fruit. ‘D’Anjou’ pears harvested at commercial and late maturity were treated with 1-MCP at 0.15 μL L⁻¹ and stored either at the commercial storage temperature −1.1 °C (1-MCP@−1.1 °C), or at 1.1 °C (1-MCP@1.1 °C) or 2.2 °C (1-MCP@2.2 °C) for 8 months. Control fruit stored at −1.1 °C ripened and developed significant scald within 7 d at 20 °C following 3–5 months of storage. While 1-MCP@−1.1 °C fruit did not develop ripening capacity due to extremely low internal ethylene concentration (IEC) and ethylene production rate for 8 months, 1-MCP@1.1 °C fruit produced significant amounts of IEC during storage and developed ripening capacity with relatively low levels of scald within 7 d at 20 °C following 6–8 months of storage. 1-MCP@2.2 °C fruit lost quality quickly during storage. Compared to the control, the expression of ethylene synthesis (PcACS1, PcACO1) and signal (PcETR1, PcETR2) genes was stable at extremely low levels in 1-MCP@−1.1 °C fruit. In contrast, they increased expression after 4 or 5 months of storage in 1-MCP@1.1 °C fruit. Other genes (PcCTR1, PcACS2, PcACS4 and PcACS5) remained at very low expression regardless of fruit capacity to ripen. A storage temperature of 1.1 °C can facilitate initiation of ripening capacity in 1-MCP treated ‘d’Anjou’ pears with relatively low scald incidence following 6–8 months storage through recovering the expression of certain ethylene synthesis and signal genes.     

Correlation and path-coefficient analyses of ripening attributes and storage disorders in ‘Ambrosia’ and ‘Empire’ apples

The objectives of this study were: (1) to determine correlation effects among the ripening attributes of ‘Empire’ and ‘Ambrosia’ apples during storage, and (2) to determine the direct and indirect contributions of these ripening attributes on the incidence of physiological disorders and storage rots using path-coefficient analysis. The analysis was applied to data obtained from a variety of harvest dates and storage regimes from apples. Pearson correlation analysis of the data indicated a strong positive correlation between internal ethylene concentration (IEC) and peel greasiness, a negative correlation between IEC and soluble solids concentration, and a negative correlation between firmness and peel greasiness in both cultivars, as well as a negative correlation between IEC and firmness in ‘Empire’. Results indicated that increased IEC in ‘Ambrosia’ apples during storage was related to higher incidences of core browning and lenticel damage and lower incidence of internal browning. Higher IEC in ‘Empire’ apples during storage was associated with less internal browning. Several significant correlations, representing different relationships among the ripening attributes and storage disorders were obtained.     

Biochemical and proteomic analysis of ‘Kyoho’ grape (Vitis labruscana) berries during cold storage

Low temperature storage is widely used to maintain the quality of postharvest fruit and extend their shelf-life. In this study, changes in specific metabolites and protein expression profiles of grape berries under cold storage were investigated by liquid chromatography and proteomic studies, respectively. During cold storage, total soluble solids and reducing sugars accumulation was accompanied by a decline in organic acids and phenols contents. A comparative analysis of the proteomes of grape berries during cold storage was performed using a two-dimensional electrophoresis (2-DE) proteomic approach. Seventy-nine differentially regulated proteins during cold storage were successfully identified by matrix-assisted laser desorption/ionization time of flight (MALDI-TOF) mass spectrometry, and classified into eight main categories based on their biological function. Down-regulation of proteins associated with glycolysis and the Krebs cycle, and up-regulation of cell wall polysaccharide degradation-related enzymes provided molecular evidence that soluble sugar and carbohydrate metabolism play a crucial role in postharvest regulation. In addition, cold storage increased the expression abundance of several stress related proteins such as heat shock proteins, proteasome and antioxidant enzymes, suggesting a physiological adaptation to low temperature was induced in grape berries. This study contributes to a better understanding of the cellular events in grape berries under cold storage and provides potentially useful information for maintaining fruit quality and minimizing postharvest losses.     

Low-temperature induction of ripening capacity in ‘Comice’ and ‘Bosc’ pears as influenced by fruit maturity

The relationship between fruit maturity at harvest and the duration of postharvest exposure to ?1 °C required to induce ripening capacity was studied in ‘Comice’ and ‘Bosc’ pears. As fruit of both cultivars were harvested progressively later, shorter durations of exposure to ?1 °C were required to induce ripening capacity. The relationship between the duration of conditioning at ?1 °C and the fruit flesh firmness after 7 d at 20 °C was well-described by second-order polynomial equations. These equations were used to determine the number of days at ?1 °C required to induce ripening capacity for each harvest date. A linear relationship was observed between the number of days after fruit in the orchard reached maturity that fruit were harvested and the number of days of low-temperature conditioning needed to induce ripening capacity. This relationship may be used to predictively estimate the duration of low-temperature conditioning required to induce ripening based on harvest date.