Proceedings
of The World Avocado Congress III, 1995 pp. 331 - 334
FACTORS
AFFECTING THE ASSESSMENT OF AVOCADO RIPENESS
Anne White and Glen Hopkirk
The
Horticulture and Food Research Institute of New Zealand
Private
Bag 92169, Auckland
New Zealand
Abstract
Firmness of avocado fruit, cv
Hass, was assessed by hand, and by whole fruit compression and puncture tests
using an Instron. The puncture test detected softening to a greater extent than
the whole fruit compression test, but neither was as good as gentle hand squeezing
by an experienced assessor.
Variability in softening and
quality of ripe fruit was examined in relation to harvest date, tree effects,
response to postharvest ethylene application, and rate of ripening. Both tree
and harvest date influenced rate of ripening and internal fruit quality, and
there was more variation within than between trees. Fruit which ripened rapidly
were of better quality than those which ripened slowly, and different pathogens
were isolated from rapid versus slow ripening fruit. The application of
ethylene after storage accelerated ripening on only one of the three harvest
occasions, and variability between fruit in both rate of ripening and internal
quality was not reduced by this treatment. The incidence of rots was not consistently
influenced by ethylene.
1. Introduction
The principal
aim of our research is to improve ripe fruit quality of Hass avocados. Since
fruit quality decreases markedly with increasing ripeness (Darvas et al.,
1990), it is important to assess the quality of individual fruit at the same
stage of ripeness. It is also important to examine different methods of
assessing ripeness. Fruit firmness is the most appropriate method of
determining ripeness. Generally, whole fruit compression (Swarts, 1981) or hand
squeezing (Hopkirk et al., 1994) have been used.
Quality and
shelf life of fruit can be affected by a large number of pre- and postharvest
factors. With the cultivar Fuerte it has been found that fruit harvested later
in the season have a decreased shelf life (Cutting et al., 1988), and high
yielding trees produce fruit with a shorter shelf life and more internal
browning (Cutting and Vorster, 1991). Hass fruit treated with ethylene 2 days
after harvest, were found to ripen more uniformly and have a shorter shelf life
than fruit ripened without ethylene (Gazit and Blumenfeld, 1970). In our study
we have investigated the use of two instrumental methods to measure firmness
and a number of factors which could affect variability between fruit including;
harvest date, inter-tree effect, ethylene treatment and rate of fruit ripening.
2.
Materials and Methods
2.1. Fruit material
Export-quality avocado (Persea
americana, cv. Hass) fruit, were harvested from mature trees commercially grown
in the Bay of Plenty, New Zealand on three occasions; 12 November 1991, 8
January and 3 February 1992. Fruit were harvested from the same 10 trees on
each occasion, dipped in the fungicide Prochloraz (250 ppm a.i., 1 min), graded
and packed into single layer trays, and 48 hours after harvest, placed into
coolstorage at 6ºC for 7 days. Upon removal from coolstorage half the fruit
were treated with ethylene (100 ppm at 20ºC for 24 h) and all fruit were
ripened in trays at 20ºC. During ripening each fruit was assessed by gentle
hand-squeezing by one trained assessor to gauge the state of ripeness. When
each individual fruit was judged to be 'fully ripe' it was assessed for rots
and disorders as described in Hopkirk et al. (1994). Analysis of variance was undertaken
on angular transformations of the percentage of fruit with unacceptable levels
of a disorder (>1.5 on a scale of 0-3); data presented are back-transformed
means. Isolations of fungi causing rots were made onto potato dextrose agar
from samples of diseased fruit, to aid identification.
2.2. Instrumental
measurement of fruit firmness
Six days (seven for harvest
2) after removal from coolstorage, 40-80 ethylene- ripened fruit were assessed
for firmness by gentle hand squeezing before using an Instron Universal Testing
Machine to measure whole fruit compression and puncture force. Intact fruit
were compressed 2 mm between 2 flat plates (traveling at a rate of 20 mm/min)
at 3 locations around the widest pan of the fruit. Skin was removed from each
of these locations, and a 7.9 mm diameter Effegi probe driven 8 mm into the
flesh at a rate of 240 mm/min.
3. Results and Discussion
3. 1. Instrumental
measurement of fruit ripeness
In general, results obtained
using the Instron puncture test were slightly better correlated with hand
assessment gradings, and less variable than results obtained using the whole
fruit compression test (average R2=0.19, standard deviation
estimate for individual values (SD)=0.55, and R2=0. 15, SD=2.06 respectively). Compression and puncture values obtained for
the same fruit were not well correlated with each other (average R2 for three harvests 0.34, SD=0.42). Compression values tended to be less
variable both within and between fruit (i.e. lower coefficient of variation)
than puncture values measured for the same fruit.
In conclusion, we feel that
neither of the instrumental measurements of firmness used in this study were
able to accurately reflect firmness as determined by gentle hand squeezing by
an experienced assessor. While the Instron compression test appeared to be
non-destructive, our experience was that the test caused some damage and
additional softening, particularly when the fruit was already ripe. Both skin
thickness and rots can influence readings obtained using an objective test, but a human
assessor is able to make allowances for skin thickness and integrate fruit
quality over the entire fruit surface rather than at specific points on the
fruit.
3.2. Factors affecting
fruit variability
Shelf life of naturally ripened
fruit decreased during the season (Table 1). The incidence of rots and internal
browning was similar on each harvest occasion.
On all three harvest
occasions fruit from tree 9, and to a lesser extent tree 1, tended to ripen
more quickly, have less rots and more internal browning disorders than fruit
from other trees (data not shown). These cases where fruit from one tree tended
to be consistently different from fruit from other trees were rare, due to the
large amount of variability within a tree compared to variability between trees
(average coefficient of variation for incidence of rots in fruit from harvest 1
was 70.2% and 39.7% respectively).
We anticipated that treatment
with ethylene would accelerate the ripening of the fruit considerably. In November,
ethylene accelerated ripening at 20ºC by 1.8 days, but on the subsequent two
harvest occasions, ethylene-treated fruit ripened no more quickly than fruit
ripened naturally (Table 1). In addition, the spread of ripening and
variability in the incidence of rots between individual fruit ripened with
ethylene was no less than that in fruit ripened naturally. On two of the three
harvest occasions B. parva was isolated mainly from the naturally
ripened fruit and C. gleosporioides
from ethylene-ripened fruit. Ethylene did not significantly influence the
incidence of rots or internal browning disorders.
The incidence of both stem
end and body rots increased as the time to ripen increased. For example, fruit
from the second harvest which ripened after 6 days at 20ºC had an incidence of
5% stem end rots and 12% body rots, whereas fruit which ripened after 12 days
had an incidence of 48% stem end rots and 73% body rots. On all three harvest
occasions, rots in individual fruit which ripened first were predominantly
caused by Botryosphaeria parva and most of the rots in late ripening
fruit were caused by Colletotrichum gleosporioides. In general, B.
parva was isolated with equal frequency from both stem end and body rots
but C. gleosporioides was isolated
predominantly from body rots.
In conclusion, it appears
that the effect of ethylene is variable and differs during the season. Despite
the fact that fruit were harvested from the same 10 trees on each harvest
occasion, there was large variability between apparently similar individual
fruit, which made it difficult to obtain consistent results for fruit treated
in various ways. Our results have highlighted the importance of assessing fruit
at the same stage of ripeness, to improve consistency of results in studies of
factors affecting fruit quality.
References
Cutting,
J.G.M., Bower, J.P., and Wolstenholme, B.N., 1988. Effect of harvest date and
applied ABA on polyphenol oxidase levels in avocado (Persea americana Mill.)
fruit. J. Hort. Sci., 63:509-515.
Cutting, J.G.M., and Vorster,
L.L., 1991. Progress report: difference in fruit ripening and quality from
trees with different yield. S. Afr. Avo. Gro. Assoc. Yearb., 14:56.
Darvas, J.M.,
Kotze, J.M., and Wehner, F.C. 1990. Effect of treatment after picking on the
incidence of postharvest fruit disease of avocado. Phytophylactica, 22:93-96.
Gazit, S., and
Blumenfeld, A., 1970. Response of mature avocado fruits to ethylene treatments
before and after harvest. J. Amer. Soc. Hort. Sci., 95(2):229-231.
Hopkirk, G., White, A.,
Beever, D.J., and Forbes, S.K., 1994. Influence of postharvest temperatures and
the rate of fruit ripening on internal postharvest rots and disor@ s of New
Zealand 'Hass' avocado fruit. N.Z. J. Crop. Hort. Sci., 22:305-311.
Swarts, D.H.,
1981. Fermometer-ondersoeke by avokado's. In: S. Afr. Avo. Gro. Assoc. Yearb.,
4:42-46.
Acknowledgements
We gratefully acknowledge the
New Zealand Avocado Export Council for funding this study. Shelley Forbes, Dave
Beever and Bill Hartill are thanked for their contribution.