Abstract:
Difficulties in controlling and forecasting avocado fruit ripening and the highly
perishable nature of the crop once harvested, are the major causes of concern for
avocado traders. In particular, the simultaneous presence of many suppliers may
account for increased fruit variability during ripening. Avocado is a climacteric fruit
with consistent ethylene production after harvest which is also related to high
perishability. However, the mechanisms regulating ethylene biosynthesis and mesocarp
softening are not completely understood.
In order to study such effects, avocado fruit from different growing areas and
harvested at various maturity stages, were investigated and the biochemical and
physiological changes during ripening at both 18 and 23°C were studied. Mesocarp
softening and fatty acid content discriminated fruit maturity and growing area,
respectively, whereas C7 sugars (D-mannoheptulose and perseitol) discriminated length
of fruit shelf life. For the first time, oleic acid content presents in the oil mesocarp was
found to depend on fruit sources making of this a suitable indicator of avocado fruit
growing area. In contrast, sugar content declined along fruit maturity and ripening. In
particular the mannoheptulose presents in avocado mesocarp might be use to estimate
avocado fruit shelf life. Indeed, fruit harvested late in season were found to have a lower
C7 content than earlier harvest fruit and a faster softening, regardless fruit source.
However, sugars content changed between growing area, thus a general C7 threshold
defining fruit storability seems to be not definable. Furthermore, other possible
indicators of fruit maturity and/or ripening stage have been searched in the cell wall
constituents of avocado mesocarp. Thus, the structural carbohydrates profile of avocado
mesocarp investigated with a new immunological method changed during ripening and
harvest time (early and late season), suggesting a possible effect of cell wall
composition on fruit ripening regulation.
Also, the possible use of ethylene application in reducing the high heterogeneity
noted on imported fruit from South Africa was also evaluated through different
consignments. Results showed ethylene efficacy changed depending on harvest time
and fruit dimension with less efficacy of the treatment on fruit harvested at the end of
the season and characterised by smaller size.One of the most commercialized avocado cultivars, Hass, is peculiar in that its
skin colour changes from green to deep purple as ripening progresses. The most
common ripening indicator of avocado fruit is the mesocarp firmness and the
destructive nature of this evaluation increases losses in the avocado industry. The
availability of a non-destructive indicator of fruit ripening represents an important
advantage for avocado consumers and importers. Thus, the possible relationship
between mesocarp softening, skin colour were objectively evaluated (C*, L*, and H°),
and the main pigment, cyanidin 3-O-glucoside, was investigated. Cyanidin 3-Oglucoside
was confirmed to be the main anthocyanin present in avocado cv. Hass peel,
regardless of preharvest factors. However, differences in its content were noted between
shelf life temperatures. A higher relationship between hue angle and firmness was
detected in late harvest fruit, whereas no correlation was found between anthocyanin
content and firmness. Avocado skin is also involved in defence mechanisms due to the
presence of antifungal and phenolic compounds. These phenolic compounds represent a
natural protection against pathogenic infections and seem to be down regulated during
ripening. The main phenolics were identified and quantified, using a new analytical
method which was validated and optimised. Epicatechin, chlorogenic acid and
procyanidin B2 were found to be present in the skin tissue and quantified using this
assay and found to vary during shelf life and seasons. Although phenolics were present
in minor amounts, in avocado pulp they are involved in mesocarp discoloration
incidence, and therefore with fruit postharvest quality. Due to a lack of information, a
new straightforward method for the identification and quantification of the main
phenolics present in avocado mesocarp was developed. Finally, a commercial trial was
undertaken to ensure that the results obtained in the laboratory can be reproduced in the
market place.
In conclusion, postharvest markers can define avocado fruit maturity and growing
area and give guidelines in the control of avocado shelf life. Moreover, new methods for
the investigation of the phenolic profiles (peel and mesocarp) and the characterisation of
cell wall structures can be further tools in the management of avocado fruit postharvest
quality.