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

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FREEDOM PALESTINE FREEDOM PALESTINE FREEDOM PALESTINE<br />

<strong>Post</strong><strong>harvest</strong> Disease Summary 295<br />

mycotoxin, <strong>and</strong> the amounts produced were considerably reduced, as<br />

compared with production in air. Sommer et al. (1974) found that two<br />

strains of P. expansum produced patuHn in Golden Delicious apples<br />

stored in a controlled atmosphere containing 7.5% CO2 <strong>and</strong> 2% O2 at<br />

23°C, although at markedly lower levels than in air. Working with other<br />

P. expansum strains, Paster et al. (1995) found that patulin production<br />

was inhibited in Starking apples stored in an atmosphere of 3% CO2, 2%<br />

O2 at 25°C, although fungal growth was still 70% of that of the control.<br />

Under 3% CO2, 10% O2, patulin production was only slightly reduced.<br />

B. Botrytis cinerea Pers. [perfect state: Botryotinia fuckeliana (de<br />

Bary) Whetzel]<br />

The gray mold rot caused by this fungus can cause heavy losses of<br />

pome <strong>fruits</strong>, particularly pears. The fungus survives as sclerotia in the<br />

soil <strong>and</strong> on plant debris, <strong>and</strong> under favorable conditions asexual spores<br />

(conidia) are formed. Under wet conditions the conidia may infect dying<br />

blossoms (Combrink et al., 1983) <strong>and</strong> remain quiescent in the flower<br />

parts (DeKock <strong>and</strong> Holz, 1991). Fruit infection occurs later, after renewal<br />

of the pathogen growth during storage <strong>and</strong> marketing. B. cinerea can<br />

infect the fruit through wounds incurred during <strong>harvest</strong>ing <strong>and</strong><br />

h<strong>and</strong>ling, or directly via skin breaks (Spotts <strong>and</strong> Peters, 1982a). In fact,<br />

the resistance of various apple cultivars to infection by B, cinerea <strong>and</strong><br />

other wound pathogens has recently been related to the force required to<br />

break the fruit skin (Spotts et al., 1999).<br />

Lesions are dry <strong>and</strong> firm at first, but become soft as the rot advances.<br />

Under humid conditions, abundant gray-brown conidia are produced.<br />

Sclerotia may also be formed on well advanced lesions. The fungus<br />

spreads very readily during storage by contact between infected <strong>and</strong><br />

sound fruit, forming 'nests* of decaying fruit. This type of infection<br />

markedly increases the infection rate in storage (Edney, 1978). In<br />

addition, J5. cinerea may penetrate apple <strong>fruits</strong> via the sinus between the<br />

calyx <strong>and</strong> the core cavity, in apple cultivars characterized by open<br />

sinuses, resulting in core rot (Spotts et al., 1988).<br />

C. Monilinia spp.<br />

Monilinia rot may be incited by three species of Monilinia: Monilinia<br />

fructigena (Aderh. & Ruhl.) Honey, which is widespread in Europe, Asia<br />

<strong>and</strong> South America, but is uncommon in North America; M fructicola<br />

(Wint.) Honey, which occurs in North <strong>and</strong> South America, South Africa,<br />

Japan, Australia <strong>and</strong> New Zeal<strong>and</strong>; <strong>and</strong> Monilinia laxa (Aderh. & Ruhl.)<br />

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