Aqueous 1-Methylcyclopropene Extends Longevity and Does Not Affect Sensory Acceptability of Guatemalan-West Indian Hybrid Avocado

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Marcio Eduardo Canto Pereira 1Horticultural Sciences Department, University of Florida-IFAS, P.O. Box 110690, Gainesville, FL 32611

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Steven A. Sargent 1Horticultural Sciences Department, University of Florida-IFAS, P.O. Box 110690, Gainesville, FL 32611

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Charles A. Sims 2Food Science and Human Nutrition Department, University of Florida-IFAS, Gainesville, FL 32611

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Donald J. Huber 1Horticultural Sciences Department, University of Florida-IFAS, P.O. Box 110690, Gainesville, FL 32611

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Celso Luiz Moretti 3Embrapa Hortaliças, Gama, DF, 70359-970, Brazil

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Jonathan H. Crane 4Horticultural Sciences Department, University of Florida-IFAS, Tropical Research and Education Center, Homestead, FL 33031

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Abstract

The ethylene inhibitor 1-methylcyclopropene (1-MCP) delays ripening of avocado (Persea americana) and many other fruits, but there are few reports of the influence of this ethylene inhibitor on sensory attributes. The objective of this study was to evaluate the effects of aqueous 1-MCP on fruit ripening and sensory attributes of ‘Beta’ avocado, a Guatemalan-West Indian hybrid. Treatment with aqueous 1-MCP at 2.77 μmol·L−1 (150 μg·L−1) for 1 minute effectively delayed ripening by 6 days, delaying the onset of climacteric and lowering respiration rates as compared with control. Treated fruit had greener peel and firmer pulp when ripe, and untrained sensory panelists could not detect differences in texture, flavor, and overall liking between treated and untreated fruit. Immersion of ‘Beta’ avocado in aqueous 1-MCP extended the shelf life to 14 days at 20 °C and 84% relative humidity, an increase of 6 days (75%) as compared with untreated fruit, without compromising sensory acceptability. This technology has the potential to permit shipment of these fruit to more distant markets than currently possible.

Avocado is a climacteric fruit (Eaks, 1978) characterized by the accumulation of oil while attached to the plant and by various potential cancer-preventing phytochemicals (Ding et al., 2007). There are three known races of avocado: West Indian, Guatemalan, and Mexican. Cold tolerance and oil content are higher for Mexican avocados and lower for West Indian avocados, while Guatemalan fruit are intermediate. Mexican types are smaller than West Indian or Guatemalan fruit, which are usually green-skinned and large (Crane et al., 2007). Many commercial cultivars are hybrids between two of these races.

Although there are many published reports for cultivars of the Mexican race, there is a lack of information on cultivars grown in the lowland tropics and subtropics that are crosses of the West Indian and Guatemalan races. These types are the main avocado cultivars produced in many tropical regions around the globe and represent significant sales for both domestic and export markets. Major producers of these tropical/subtropical types are the Dominican Republic (295,000 t), Indonesia (276,000 t) (Food and Agriculture Organization of the United Nations, 2013), and Brazil [160,000 t (Instituto Brasileiro de Geografia e Estatística, 2013)] in 2011. Florida accounted for 13.7% (28,100 t) of total U.S. production with a value of $23.5 million during 2011–12 season (U.S. Department of Agriculture, 2013). The bulk of the avocado produced in Florida is sold outside the state, contributing significantly as a revenue generator for Florida. Florida avocados have the nutritional appeal of lower oil and lower calorie content than the ‘Hass’, which has been a great marketing tool for the Florida avocado industry, which is investing on fruit quality, shelf life extension and year-round availability (Crane et al., 2007). An extension of its shipping life would also represent an extension of marketing possibilities.

The hormone ethylene (C2H4) is essential for avocado ripening (Zauberman et al., 1988) and controlling its action is critical to extend postharvest life. The ethylene inhibitor 1-MCP has been largely used in research to better understand ripening and senescence in many horticultural crops (Huber, 2008; Watkins, 2008). For avocado, gaseous 1-MCP effectively delayed ripening in concentrations ranging from 30 to 500 nL·L−1 following 24-h exposure at 20 °C (Adkins et al., 2005; Feng et al., 2000; Jeong et al., 2002; Kluge et al., 2002). Treatment effects reported by these authors include reduced ethylene evolution and respiration, delayed softening and suppression of polygalacturonase activity in avocado.

Aqueous 1-MCP, originally formulated for preharvest application (Blankenship and Dole, 2003), was also found to be effective as a postharvest treatment for tomato (Solanum lycopersicum) (Choi and Huber, 2008), the Mexican-Guatemalan hybrid avocado ‘Hass’ (Choi et al., 2008), and the Guatemalan-West Indian hybrid avocado ‘Booth 7’ (Zhang et al., 2011). The aqueous formulation of 1-MCP has the potential to be applied directly to the fruit, thus eliminating the need for lengthy exposure in sealed facilities that is required for gaseous 1-MCP treatment. Although 1-MCP has been reported to negatively affect the sensory acceptability of some fruit, notably apples [Malus sylvestris (Marin et al., 2009)] and bananas [Musa sp. (Pinheiro et al., 2010)], there have been no reports of the effect of 1-MCP on sensory quality of avocado.

The objective of this work was to evaluate ripening parameters and sensory acceptability of the Guatemalan-West Indian hybrid avocado ‘Beta’ treated with aqueous 1-MCP.

Material and methods

Plant material

‘Beta’ avocado fruit were harvested early in the morning at the preclimacteric stage from an experimental planting located at the Tropical Research and Education Center (Homestead, FL) during harvesting date C (Sept. 2008). The Florida Avocado Administrative Committee establishes official harvesting dates (A to D) required for each commercial avocado cultivar grown in Florida based on minimum size and weight requirements. Harvesting date C refers to the third harvesting date (Florida Avocado Administrative Committee, 2008). After harvest, fruit were immediately transported to the Postharvest Horticulture Laboratory of the University of Florida, Gainesville, and stored at 20 °C overnight. The following day, sound fruit were randomized into groups for treatment application.

2.2 Aqueous 1-MCP treatment

Aqueous 1-MCP was prepared from formulation AFxRD-300 (2% a.i.; AgroFresh, Philadelphia, PA) according to Choi and Huber (2008). To prepare the aqueous 1-MCP solution, AFxRD-300 powder was diluted in 30 L of deionized water at 20 °C. The solution was used from 10 to 45 min after preparation (Choi et al., 2008). Fruit were placed in mesh bags and completely immersed for 1 min in the aqueous 1-MCP solution at a concentration of 2.77 μmol·L−1. Bags were gently agitated to ensure full contact of solution with fruit surface. Immediately after immersion, excess solution was drained, fruit were removed from the bags, and were dried with paper towels and stored uncovered in a single layer on trays at 20 °C and 92% ± 3% relative humidity. Control fruit (immersed in water only, not exposed to 1-MCP) were stored under identical conditions. Initial quality analysis was conducted on the same day for untreated fruit.

Ripening and quality parameters

Whole fruit firmness.

Whole fruit firmness was determined nondestructively during ripening, adapting the method described by Jeong et al. (2002). A nondestructive compression test was performed on whole, unpeeled fruit using a universal testing instrument (model 4411; Instron, Norwood, MA) fitted with a flat-plate probe (5 cm diameter) and 0.5-kN load cell. After establishing zero force contact between the probe and the equatorial region of the fruit, the probe was driven with a crosshead speed of 0.33 mm·s−1. The force was recorded at 2.5-mm deformation and was determined at two points on the equatorial region of each fruit, with a 90° angle between the points. The same 10 fruit for each treatment were measured every other day and were considered at the ripe stage (limit of commercial marketability) upon reaching 10 to 15 N firmness.

Ethylene evolution and respiration.

Ethylene evolution and respiration rates [as carbon dioxide (CO2) evolution] were measured daily on five individual fruit per treatment. Each fruit was sealed for 20 min in a 2-L plastic container before sampling. A 1 mL gas sample was withdrawn by a plastic syringe through a rubber septum for analysis using gas chromatography as described by Jeong et al. (2002).

Weight loss.

Percent weight loss was calculated considering the fruit weight loss from the beginning of the experiment until the ripe stage. This calculation was performed for the same 10 fruit used for whole fruit firmness determination.

Peel and pulp color.

The same fruit used for whole fruit firmness determination were also used when ripe to measure peel and pulp color (after cross sectioning the fruit) at the equatorial region (two readings per fruit) with a colorimeter (model CR-400; Konica Minolta, Tokyo, Japan). The colorimeter was calibrated with a white standard tile. The results are presented as lightness (L*), chromaticity value (C*) and hue angle.

Pulp hardness.

This analysis was performed by using the samples from ripe mesocarp tissue to simulate the two first bites of a consumer, adapting the texture profile analysis methodology described by Yagiz et al. (2007). For each treatment, a cross-section (10 mm thick) was removed from stem end, equatorial, and blossom end of the fruit (n = 3 fruit). From each slice, three cylindrical samples (10 mm diameter × 10 mm length) were withdrawn with a cork borer from the stem-end to blossom-end orientation. Each mesocarp sample was placed vertically (same sampling direction) on a flat aluminum plate and submitted to the pulp hardness test using a universal testing instrument (model 4411) fitted with a flat cylindrical probe (13 mm diameter) and 0.02-kN load cell. After establishing zero force contact between the probe and the top surface of the cylindrical sample, the probe was driven with a crosshead speed of 3.3 mm·s−1 to 70% of original sample height. There were two consecutive compression-decompression cycles per test. The hardness of the first and second cycles was determined using Blue Hill software (Instron).

Sensory analysis.

The consumer sensory acceptance test was conducted in the sensory laboratory of the Food Science and Human Nutrition Department at the University of Florida. Fruit from each treatment were evaluated on the day the fruit reached the ripe stage. Fruit were sliced longitudinally in quarters, peeled, and the pulp was sliced into pieces of 2 × 2 ×1 cm. Each panelist sat in an individual booth and received two pieces of avocado pulp served in plastic cups labeled with three digit random numbers. They were asked to evaluate texture, flavor, and overall liking using a nine-point hedonic scale where 1 = dislike extremely, 5 = neither like nor dislike, and 9 = like extremely. Scores and comments were recorded directly into a computer using the software Compusense five (version 4.8.8; Compusense, Guelph, ON, Canada).

Statistical analysis

The experiment was conducted using a completely randomized design with two treatments (untreated control and 1-MCP treated). Number of replicates varied according to analysis: 10 replicates for whole fruit firmness, weight loss, and peel and pulp color; five replicates for ethylene evolution and respiration determination; three replicates for pulp hardness; and 75 untrained panelists for sensory analysis. Data from sensory analysis were analyzed by one-way analysis of variance. Statistical procedures were performed using SAS (version 9.1.3; SAS Institute, Cary, NC). Differences between means were determined using Duncan’s multiple range test.

Results

Untreated ‘Beta’ avocado softened rapidly from initial firmness 140 N to 22 N within 6 d and reached the ripe stage (10 to 15 N) after 8 d of storage (Fig. 1). Treatment with 1-MCP extended the time to ripe stage to 14 d, representing a 75% shelf life extension.

Fig. 1.
Fig. 1.

Whole fruit firmness of untreated ‘Beta’ avocados (control) or following immersion at preclimacteric stage in aqueous 1-methylcyclopropene (1-MCP) solution 2.77 μmol·L−1 [150 μg·L−1 (ppb)] for 1 min and storage at 20 °C (68.0 °F). Vertical bars represent ±se (n = 10). Dotted line represent firmness threshold (15 N) for ripe fruit; 1 N = 0.2248 lbf.

Citation: HortTechnology hortte 23, 4; 10.21273/HORTTECH.23.4.468

Initial softening occurred for control and for 1-MCP-treated fruit within the first 3 d of storage, however, at low levels of ethylene production [< 0.4 ng·kg−1·s−1 (Fig. 2A)]. From that point ethylene production in control fruit significantly increased from 0.2 ng·kg−1·s−1 to a peak at 78 ng·kg−1·s−1 on day five, then decreased to 10 ng·kg−1·s−1 by the ripe stage. Fruit treated with 1-MCP exhibited increased ethylene evolution after 2 d of storage and peaked at 83 ng·kg−1·s−1 on day nine. The 1-MCP treatment delayed the climacteric rise of ethylene evolution by 4 d, but the pattern and the levels of production were very similar to untreated fruit. In addition, it is worth mentioning that firmness of both control and 1-MCP-treated fruit was similar, nearly 40 N, at peak ethylene evolution.

Fig. 2.
Fig. 2.

Ethylene evolution (A) and respiratory rates (B) [as carbon dioxide (CO2) evolution] of untreated ‘Beta’ avocados (control) or following immersion at preclimacteric stage in aqueous 1-methylcyclopropene (1-MCP) solution at 2.77 μmol·L−1 [150 μg·L−1 (ppb)] for 1 min and storage at 20 °C (68.0 °F). Vertical bars represent ±se (n = 5); 1 μg·kg−1 = 1 ppb, 1 ng·kg−1 = 0.001 ppb.

Citation: HortTechnology hortte 23, 4; 10.21273/HORTTECH.23.4.468

Respiratory rates of untreated fruit peaked at 51 μg·kg−1·s−1 within 4 d of storage (Fig. 2B). For treated fruit, the increase in respiratory activity was slower than control fruit, peaking after 7 d at 41 μg·kg−1·s−1, 20% lower than untreated fruit.

Control fruit retained ≈26% more fresh weight than 1-MCP-treated fruit when ripe (Table 1). However, the peel color of treated fruit was greener (higher hue value) and darker (lower L* value) than control fruit (Table 1); no differences were found for pulp color.

Table 1.

Weight loss and peel color of ripe ‘Beta’ avocados untreated (control) or following immersion at preclimacteric stage in aqueous 1-methylcyclopropene (1-MCP) solution 2.77 μmol·L−1 [150 μg·L−1 (ppb)] for 1 min and storage at 20 °C (68.0 °F).

Table 1.

The analysis of pulp hardness of ripe fruit showed that pulp in the apical cross-section of untreated fruit was firmer than that from the equatorial and distal-end sections (Table 2). Treatment with 1-MCP exacerbated within fruit difference among sections, where pulp hardness at the apical end was 176% higher than that from the distal end; this difference was only 28% within untreated fruit. Pulp from all the three sections was harder in 1-MCP-treated than the corresponding section from untreated fruit.

Table 2.

Hardness of segments of ripe mesocarp tissue taken from stem end (apical end), equatorial and blossom end (distal end) cross-sections of untreated ‘Beta’ avocados (control) or following immersion at preclimacteric stage in aqueous 1-methylcyclopropene (1-MCP) solution 2.77 μmol·L−1 [150 μg·L−1 (ppb)] for 1 min and storage at 20 °C (68.0 °F).

Table 2.

Sensory analysis performed by 75 untrained panelists showed no significant differences between 1-MCP-treated and non-treated ‘Beta’ avocado for all attributes tested (Table 3).

Table 3.

Average texture, flavor, and overall liking scores from 75 untrained panelists for ripe, untreated ‘Beta’ avocados (control) or following immersion at preclimacteric stage in aqueous 1-methylcyclopropene (1-MCP) solution 2.77 μmol·L−1 [150 μg·L−1 (ppb)] for 1 min and storage at 20 °C (68.0 °F).

Table 3.

Discussion

Avocado is a climacteric fruit that requires ethylene to ripen (Zauberman et al., 1988) and responds best to 1-MCP treatment when preclimacteric (Zhang et al., 2011). This benefit of 1-MCP has been reported for gaseous treatments of avocado at 50 to 900 nL·L−1 for 12 h to 24 h, with 50% to 75% increase in shelf life (Adkins et al., 2005; Feng et al., 2000; Jeong et al., 2002; Jeong and Huber, 2004; Kluge et al., 2002). There was a 75% extension of time to ripe stage observed in this study for aqueous 1-MCP-treated ‘Beta’ avocado as compared with control. This is an impressive result because the success of 1-MCP treatment depends, among other factors, on 1-MCP concentration and cultivar. Treatments with aqueous 1-MCP at 1.39 and 2.77 μmol·L−1, respectively, delayed ripening of ‘Simmonds’ by 33% and 67%, ‘Booth 7’ by 40% and 80%, and ‘Monroe’ by 50% to 83% (Pereira et al., 2013). This result clearly shows the potential to use aqueous formulation of 1-MCP, a postharvest treatment for avocado.

Despite the strong effect of 1-MCP in delaying ‘Beta’ avocado softening, a significant part of initial softening occurred during nonevident climacteric evolution of ethylene. This may be due to either ethylene-independent, softening-related events that occur despite the presence of an ethylene inhibitor or due to softening-related events that are dependent upon very low concentrations of ethylene evolution by the fruit. These mechanisms have been reported for other fruit such as apple (Tacken et al., 2010), kiwifruit [Actinidia chinensis (Mworia et al., 2011)], and melon [Cucumis melo (Nishiyama et al., 2007)]. The delay of softening caused by 1-MCP treatment was likely due to a delay in the activity of softening-related enzymes (polygalacturonase, pectin methylesterase, α- and β-galactosidases, and endo-β-1,4-glucanase) as previously shown for avocado (Jeong et al., 2002; Jeong and Huber, 2004).

In this study, the pattern and rates of respiration for ‘Beta’ avocado were more affected by aqueous 1-MCP treatment than those for ethylene evolution. Respiration rate suppression was also reported for other avocado cultivars (Choi et al., 2008; Zhang et al., 2011; Pereira et al., 2013) treated with aqueous 1-MCP and for other several commodities treated with gaseous 1-MCP (Watkins, 2006). Lower respiratory rates are directly related to a longer postharvest life in fresh produce. Despite the slower fruit metabolism indicated by lower respiration rates of 1-MCP-treated ‘Beta’ avocado, there was a complete recovery of fruit capacity to produce ethylene, as evidenced by the similar pattern and rates of ethylene evolution that occurred during storage.

Fruit appearance can be negatively affected by 1-MCP treatment; shriveling was reported by Hurr et al. (2005) due to excessive weight loss in tomato during extended ripening, as there was atypical color development in banana (Golding et al., 1998) and tomato (Hurr et al., 2005). Despite the significant higher weight loss observed for 1-MCP-treated ‘Beta’ avocado in this study, likely due to the extended storage time to reach ripeness, there was no appearance of shriveling. However, the darker and greener peel color observed in treated fruit may negatively influence the consumer’s purchase decision if based solely on peel color. ‘Beta’ avocado, a green-skinned Guatemalan-West Indian hybrid (Crane et al., 2007), remains light green or yellowish when ripe in contrast to the smaller Mexican-Guatemalan hybrid ‘Hass’ which changes from a dark green to dark purple during ripening (Ashton et al., 2006).

The analysis of ripe pulp hardness gave evidence to the occurrence of a natural ripening asynchrony in untreated control ‘Beta’ fruit, with softer pulp toward the distal end of the fruit. Treatment with 1-MCP exacerbated ripening asynchrony, increasing the difference in pulp hardness among sections, even though aqueous 1-MCP was uniformly applied over the entire fruit surface during the 1-min immersion. Ripening asynchrony was reported by Choi et al. (2008) in avocado and tomato fruit partially immersed in aqueous 1-MCP solution, without evidence of being influenced by the stem-end scar. This was unlikely due to the difference in whole fruit firmness, because actual average values for ripe fruit (11.5 N for control, 13.4 N for 1-MCP-treated) were not significantly different. The reason for the exacerbated difference observed for ‘Beta’ avocado in this study may be because of the embryonic growth, which occurs at the blossom end, accelerates ethylene sensitivity and production (Hershkovitz et al., 2009, 2010).

Despite the differences in pulp hardness, sensory analysis of ‘Beta’ avocado revealed that panelists could not distinguish between 1-MCP-treated fruit and untreated fruit. No significant effects of 1-MCP on sensory attributes were reported for other fruits such as mango [Mangifera indica (Cocozza et al., 2004)], kiwifruit (Harker et al., 2008), and tomato (Baldwin et al., 2011). However, apple (Marin et al., 2009; Pre-Aymard et al., 2005) and pear [Pyrus communis (Moya-Leon et al., 2006)] treated with 1-MCP were distinguishable from untreated fruit due to a higher fruit firmness. These latter reports show the importance of conducting sensory analyses to evaluate the consumer’s perception of 1-MCP treatment.

The results of this study are encouraging for the avocado industry. However, because this study was not repeated in space or time and will not be continued, there are limitations due to the preliminary nature of these data. Nevertheless, it is clear that this technology has the potential to be used as a postharvest treatment of avocado to permit shipment of these fruit to more distant markets than currently possible.

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  • U.S. Department of Agriculture 2013 Noncitrus fruits and nuts 2012 preliminary summary. 4 Apr. 2013. <http://usda01.library.cornell.edu/usda/current/NoncFruiNu/NoncFruiNu-01-25-2013.pdf>

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  • Watkins, C.B. 2006 The use of 1-methylcyclopropene (1-MCP) on fruits and vegetables Biotechnol. Adv. 24 389 409

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  • Yagiz, Y., Kristinsson, H.G., Balaban, M.O. & Marshall, M.R. 2007 Effect of high pressure treatment on the quality of rainbow trout (Oncorhynchus mykiss) and mahi mahi (Coryphaena hippurus) Food Chem. Technol. 72 C509 C515

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  • Zauberman, G., Fuchs, Y., Yanko, U. & Akerman, M. 1988 Response of mature avocado fruit to postharvest ethylene treatment applied immediately after harvest HortScience 23 588 589

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  • Zhang, Z., Huber, D.J. & Rao, J. 2011 Ripening delay of mid-climacteric avocado fruit in response to elevated doses of 1-methylcyclopropene and hypoxia-mediated reduction in internal ethylene concentration Postharvest Biol. Technol. 60 83 91

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  • Whole fruit firmness of untreated ‘Beta’ avocados (control) or following immersion at preclimacteric stage in aqueous 1-methylcyclopropene (1-MCP) solution 2.77 μmol·L−1 [150 μg·L−1 (ppb)] for 1 min and storage at 20 °C (68.0 °F). Vertical bars represent ±se (n = 10). Dotted line represent firmness threshold (15 N) for ripe fruit; 1 N = 0.2248 lbf.

  • Ethylene evolution (A) and respiratory rates (B) [as carbon dioxide (CO2) evolution] of untreated ‘Beta’ avocados (control) or following immersion at preclimacteric stage in aqueous 1-methylcyclopropene (1-MCP) solution at 2.77 μmol·L−1 [150 μg·L−1 (ppb)] for 1 min and storage at 20 °C (68.0 °F). Vertical bars represent ±se (n = 5); 1 μg·kg−1 = 1 ppb, 1 ng·kg−1 = 0.001 ppb.

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  • U.S. Department of Agriculture 2013 Noncitrus fruits and nuts 2012 preliminary summary. 4 Apr. 2013. <http://usda01.library.cornell.edu/usda/current/NoncFruiNu/NoncFruiNu-01-25-2013.pdf>

    • Crossref
    • Export Citation
  • Watkins, C.B. 2006 The use of 1-methylcyclopropene (1-MCP) on fruits and vegetables Biotechnol. Adv. 24 389 409

  • Watkins, C.B. 2008 Overview of 1-methylcyclopropene trials and uses for edible horticultural crops HortScience 43 86 94

  • Yagiz, Y., Kristinsson, H.G., Balaban, M.O. & Marshall, M.R. 2007 Effect of high pressure treatment on the quality of rainbow trout (Oncorhynchus mykiss) and mahi mahi (Coryphaena hippurus) Food Chem. Technol. 72 C509 C515

    • Crossref
    • Search Google Scholar
    • Export Citation
  • Zauberman, G., Fuchs, Y., Yanko, U. & Akerman, M. 1988 Response of mature avocado fruit to postharvest ethylene treatment applied immediately after harvest HortScience 23 588 589

    • Search Google Scholar
    • Export Citation
  • Zhang, Z., Huber, D.J. & Rao, J. 2011 Ripening delay of mid-climacteric avocado fruit in response to elevated doses of 1-methylcyclopropene and hypoxia-mediated reduction in internal ethylene concentration Postharvest Biol. Technol. 60 83 91

    • Search Google Scholar
    • Export Citation
Marcio Eduardo Canto Pereira 1Horticultural Sciences Department, University of Florida-IFAS, P.O. Box 110690, Gainesville, FL 32611

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Steven A. Sargent 1Horticultural Sciences Department, University of Florida-IFAS, P.O. Box 110690, Gainesville, FL 32611

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Charles A. Sims 2Food Science and Human Nutrition Department, University of Florida-IFAS, Gainesville, FL 32611

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Donald J. Huber 1Horticultural Sciences Department, University of Florida-IFAS, P.O. Box 110690, Gainesville, FL 32611

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Celso Luiz Moretti 3Embrapa Hortaliças, Gama, DF, 70359-970, Brazil

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Jonathan H. Crane 4Horticultural Sciences Department, University of Florida-IFAS, Tropical Research and Education Center, Homestead, FL 33031

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Contributor Notes

The authors gratefully acknowledge the support of Embrapa (Brazilian Agriculture Research Corporation) for the Ph.D. scholarship to the first author, AgroFresh, Inc., in providing the 1-MCP formulation for this study and to Lorenzo A. Puentes, for his dedicated work and help on the sensory analysis

Corresponding author. E-mail: marcio.pereira@embrapa.br.

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  • Whole fruit firmness of untreated ‘Beta’ avocados (control) or following immersion at preclimacteric stage in aqueous 1-methylcyclopropene (1-MCP) solution 2.77 μmol·L−1 [150 μg·L−1 (ppb)] for 1 min and storage at 20 °C (68.0 °F). Vertical bars represent ±se (n = 10). Dotted line represent firmness threshold (15 N) for ripe fruit; 1 N = 0.2248 lbf.

  • Ethylene evolution (A) and respiratory rates (B) [as carbon dioxide (CO2) evolution] of untreated ‘Beta’ avocados (control) or following immersion at preclimacteric stage in aqueous 1-methylcyclopropene (1-MCP) solution at 2.77 μmol·L−1 [150 μg·L−1 (ppb)] for 1 min and storage at 20 °C (68.0 °F). Vertical bars represent ±se (n = 5); 1 μg·kg−1 = 1 ppb, 1 ng·kg−1 = 0.001 ppb.

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