P.J. Hofman, R.L. McLauchlan and L.G. Smith
Horticulture
Postharvest Group
Department
of Primary Industries Queensland
Australia
The respiration of
individual 'Hass' and 'Fuerte' fruit was monitored during storage at 8ºC and
10ºC respectively for 14 days, under a continuous flow of humidified air containing
ethylene (C2H4)
at 0, 0.01, 0.05,
0.25, 1.0 and 5.0 μL.L-1. Respiration rates of 'Fuerte' fruit
under 0.01 μL.L-1 C2H4 were significantly higher
than the controls after 3.3 days of storage, but for 'Hass' fruit respiration rates
did not become significantly higher until under 1.0 μL.L-1 for
5.7 days.
In another experiment,
'Hass' fruit were held in the presence of 0, 35, 70, 140, 280 or 1000 g of
Purafil® (C2H4
absorbent) at
20ºC. Increasing amounts of Purafil® consistently reduced the maximum
concentration of
C2H4 detected in the storage containers. Days from harvest to maximum
detected C2H4
production rate
(MDEPR) in bulk samples was increased from 8.1 to an average of 11.1 days by
the presence of Purafil®, but increasing amounts of Purafil® had no further
effect. Fruit stored individually in ventilated containers in the absence of
Purafil® reached MDEPR on average at 13.8 days.
These results indicate that
stimulation of ripening by C2H4 evolution from earlier- ripening fruit may be
important in hastening ripening of fruit stored in bulk. Ethylene removal in
storage may offer some advantage, but concentrations may need to be reduced to
0.05 μL.L-1 or lower to obtain
significant benefit, especially for 'Fuerte'. However, storage of only those
fruit with similar storage capacity is likely to be of greater benefit. A
knowledge of production factors contributing to poor storage life is required.
1. Introduction
Avocado marketing within
Australia generally requires transport by road under cold storage temperatures
(ideally 7-10ºC) for 3-7 days, and sea freight to export markets will require
3-5 weeks storage life. Control of ripening is essential to successful
marketing under these conditions.
Ethylene plays an important
role in fruit ripening. Fruit sensitivity to C2H4 and the presence of C2H4
during storage
is generally undesirable, and reduction of C2H4 in commercial storage of
several fruits is practiced. Since avocado fruit are sensitive to C2H4 (Zauberman and Fuchs, 1973;
Adato and Gazit, 1974), their storage should benefit by control of C2H4
concentrations.
This paper describes some of the responses of avocado fruit to storage under
various conditions in relation to C2H4.
2. Materials and Methods
2.1 Experiment I
'Hass' avocado fruit were
obtained by road freight from south east Queensland, and in another experiment
'Fuerte' fruit from north Queensland by airfreight. Fruit were placed in
individual, sealed containers and ventilated with air (93-95% RH) containing 0,
0.01, 0.05, 0.25, 1.0 and 5.0 μL.L-1 C2H4, at a flow rate of 25-40
mL.min-1. Effluent gas streams from each container were connected
via a rotary gas sampling unit to an infra-red gas analyser (Horiba PIR-2000)
for carbon dioxide (CO2) analysis. Seven fruit were used for each C2H4 concentration. 'Hass' fruit
were stored at 8ºC and 'Fuerte' fruit at 10ºC, to represent typical
temperatures observed during commercial refrigerated road transport. Fruit were
removed at 14 days, and held for a further 6 days at 20ºC to ripen.
Skin colour was measured
using a Hunter Labscan 6000 0/45º spectrocolorimeter fitted with a 25 mm
orifice, D65 illuminant, and 10º observer. Fruit firmness was quantified using
an Instron Universal Testing Machine model 1122, fitted with a 12 mm
hemispherical probe (probe penetration 2 mm at 20 mm.min-1).
2.2 Experiment 2
'Hass' avocado fruit were
harvested from south east Queensland and dipped in 0.55 mL.L-1 prochloraz for 30 sec. The following day, 42 fruit were
individually weighed and sealed in separate 1.4 L respiration chambers at 20ºC,
each ventilated with 90-160 mL.min-1 C2H4-free, humidified (93% RH)
air. In addition, samples of 20 fruit were sealed in each of 6 ventilated 30 L
plastic containers, each receiving about 300 mL.min-1 C2H4-free, humidified air. Purafil® (0, 35, 70, 140, 280
and 1 000 g) was placed in each of the containers to absorb fruit-produced C2H4. The effluent gas from each
container was connected via the 50 channel rotary gas sampling unit to a
Shimadzu gas chromatograph for C2H4 analysis. The days to C2H4 peak, the maximum detected
concentration in each container, and the % dry matter (DM) of fruit at eating
soft were determined.
3. Results
3.1 Experiment I
'Fuerte' fruit showed enhanced
ripening at 10ºC (significantly higher respiration rate, and softer fruit)
under all C2H4
treatments
compared to the control (figure 1; tables 1 and 2), while 'Hass' fruit showed
similar responses only under 1 and 5 μL.L-1 C2H4 at 8ºC. Ripening was enhanced with higher C2H4 concentrations, and a
similar pattern was also evident after a further 6 days at 22ºC (data not
presented).
3.2 Experiment 2
The presence of Purafil® in
the storage container increased the time to first detected C2H4 (>
0.1 μL.kg-1.hr-1 ) and the time to maximum
detectable C2H4
production rate
(MDEPR), and decreased the MDEPR compared to the control (table 3). Increasing
amounts of Purafil® logarithmically reduced the MDEPR but had no further effect
on the time to first detectable C2H4, nor on the time to MDEPR.
Fruit from the
same harvest, when stored individually, on average reached MDEPR after 13.8
days (table 4), compared to 8.1 days for the 20 fruit stored together in the 30
L container (table 3, 0 Purafil®).
There was also considerable variation in MDEPR, days to MDEPR, and % DM between
individual fruit (table 4). No significant correlation was observed between
days to MDEPR and % DM. Similar results, indicating more rapid ripening of
fruit stored together compared to fruit stored in isolation, were obtained with
later harvests (data not presented).
4. Discussion
These results confirm avocado
sensitivity to C2H4, even at relatively low storage temperatures. The significance of these results depends on storage time, but
the enhancement of ripening noted under exposure to 1.0 and 0.01 μL.L-1 C2H4 for 'Hass' and 'Fuerte" respectively is likely to be significant in
long-term commercial storage. The apparently greater sensitivity of 'Fuerte' in
this experiment would have been slightly influenced by the higher storage
temperature used for 'Fuerte'. Possible differences in maturity between the two
cultivars may also have had an effect. However the magnitude of the difference
suggests a cultivar difference in sensitivity. The thicker skin of 'Hass' may
contribute to a reduced sensitivity to C2H4, mediated through increased
diffusive resistance to C2H4 (Banks et al., 1993).
The variation in % DM and
days to MDEPR in avocado fruit harvested on the same day and from the same
trees has also been noted by Smith et al. (1992), and in % DM and days to
eating soft in mango by Hofman et al. (1995). This has significant commercial
implications, and an attempt to reduce this variation to give uniform ripening
is one of the main reasons for the development of C2H4 ripening procedures for
avocado in Australia (Ledger and Barker, 1994). The present results also
indicate that this variability can reduce shelf life (and potentially storage
life) of bulk-stored fruit, presumably because C2H4 produced by early-ripening
fruit triggers the ripening of adjacent fruit. The ineffectiveness of
increasing amounts of Purafil®
to further increase shelf life indicates that, under the current experimental
conditions, Purafil® has only limited capacity to
remove C2H4 evolved by earlier ripening fruit, even at 1 kg Purafil® to 7 kg fruit. The results of
experiment 1 indicate that C2H4 concentrations may need to be
reduced below 1 μL.L-1 (and
possibly below 0.05 μL.L-l ) to have
reliable benefit.
Therefore, a more effective
means of increasing storage life than C2H4 removal may be to exclude
from storage those fruit which will ripen prematurely. An understanding of
factors causing variability in postharvest ripening behaviour is essential to
this, and studies to identify these pre-harvest factors are part of an ongoing
program in our laboratories.
Acknowledgments
This research was conducted
under Project 9313 of the Australian Centre for International Agricultural Research,
and project DAQ-I 17A of the Rural Industries Research and Development
Corporation. We thank Geraldine Meiburg and Leigh Barker for technical support.
References
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