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Post harvest diseases fruits and vegetables - Xavier University ...

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FREEDOM PALESTINE FREEDOM PALESTINE FREEDOM PALESTINE<br />

Physical Means 203<br />

5% even when low ethanol concentrations (2.5-5%) were used. Spore<br />

mortality of M fructicola <strong>and</strong> K stolonifer, the main post<strong>harvest</strong><br />

pathogens of peaches <strong>and</strong> nectarines, occurred much more quickly in<br />

heated ethanol than in heated water (Margosan et al., 1997): a 10%<br />

ethanol solution at 46 or 50°C greatly reduced the LT95 (95% lethality) of<br />

both fungi (Table 12).<br />

TABLE 12<br />

Estimated time (seconds) to kill 95% of the spores of Monilinia<br />

fructicola or Rhizopus stolonifer in water, alone or containing<br />

10% ethanol, at 46 or 50°C*<br />

M. fructicola R. stolonifer<br />

Treatment 46^C 50^C 46^C 50°C<br />

Water 734.0a 206.3a >1000.0a 410.3a<br />

10% ethanol 57.4b 7.0b 94.4b 46.3b<br />

* Values followed by unlike letters are significantly different (P < 0.05).<br />

Reproduced from Margosan et al., 1997 with permission of the<br />

American Phytopathological Society.<br />

When peaches <strong>and</strong> nectarines, infected with M fructicola spores, were<br />

immersed in 10% ethanol at 46 or 50°C, or 20% ethanol at 46''C the<br />

incidence of decayed fruit was 83, 25 or 12%, respectively, i.e., similar or<br />

a better control was achieved than that following a 1-min dip in the<br />

fungicide, iprodione (1000 |ag ml^). No injury to the <strong>fruits</strong> occurred <strong>and</strong><br />

no off-flavors were detected in the <strong>fruits</strong>. However, unlike fungicides, the<br />

hot ethanol treatments did not deposit persistent antifungal residues, so<br />

there was a lack of continuous protection of the <strong>fruits</strong> from<br />

recontamination.<br />

The increases in spore mortality <strong>and</strong> decay control - occurring when<br />

hot water <strong>and</strong> ethanol were combined - may result from their affecting<br />

the same sites in the spores. Since low concentrations of ethanol can<br />

lower the temperature at which phospholipids undergo a phase change<br />

(Rowe, 1983), the increases in spore mortality <strong>and</strong> decay control following<br />

the addition of ethanol may have resulted from a lowering of the<br />

phase-change temperature of the mitochondrial membranes of the spores<br />

under these conditions (Margosan et al., 1997).<br />

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