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Advances in Food Mycology

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Black Aspergillus Species <strong>in</strong> Australian V<strong>in</strong>eyards 159<br />

Harvested bunches were chilled at 4°C prior to crush<strong>in</strong>g. After<br />

crush<strong>in</strong>g, eight samples of must from each tox<strong>in</strong> level were collected <strong>in</strong><br />

order to establish the <strong>in</strong>itial total OA present <strong>in</strong> the berries. Samples<br />

were also collected throughout the v<strong>in</strong>ification process as described<br />

below.<br />

Dur<strong>in</strong>g white v<strong>in</strong>ification, the must was pressed, after which potassium<br />

metabisulphite was added to give 50 ppm SO 2 <strong>in</strong> the juice.<br />

Pect<strong>in</strong>ase was added <strong>in</strong> the form of Pomolase AC50 (0.05 ml/l<br />

juice; Enzyme Solutions, Victoria, Australia) or Pect<strong>in</strong>ase (0.5 g/l<br />

juice; Fermtech, Queensland, Australia). The juice was overlaid with<br />

nitrogen or carbon dioxide, and refrigerated at 4°C for at least 24 h to<br />

precipitate solids. In 2002, the juice was divided <strong>in</strong>to four replicate<br />

ferments at each tox<strong>in</strong> level before clarification; this division occurred<br />

after clarification <strong>in</strong> 2003. The pH was adjusted to approximately 3.3<br />

by the addition of tartaric acid to give a titratable acidity of 6.5-7.0<br />

g/l. The clarified juice was siphoned <strong>in</strong>to bottles filled with nitrogen or<br />

carbon dioxide and fitted with stoppers and air traps. The yeast QA23<br />

(Lallemand, Toulouse, France) was rehydrated and added at a rate<br />

equivalent to 0.2 g dry yeast/l juice. Diammonium phosphate was<br />

added at 0.5 g/l juice. The fermentation temperature was 19°C <strong>in</strong> 2002<br />

and 15°C <strong>in</strong> 2003. Diammonium phosphate was added dur<strong>in</strong>g fermentation<br />

as required and after fermentation was completed, the w<strong>in</strong>e<br />

was racked. Potassium metabisulphite was added at a rate equivalent<br />

to 50 ppm SO 2 to stabilise the w<strong>in</strong>e and prevent further fermentation.<br />

Bentonite (0.5 g/l; Fermtech, Queensland, Australia) and Liquif<strong>in</strong>e<br />

(2002: 1 ml/l; 2003: 0.6 ml/l; W<strong>in</strong>ery Supplies, Victoria, Australia) were<br />

added, and the bottles placed at 19°C (2002) or 15°C (2003) to allow<br />

precipitation of solids. A second rack<strong>in</strong>g was performed for all bottles,<br />

and potassium metabisulphite was added to br<strong>in</strong>g the free SO 2 to 20<br />

ppm. The bottles were placed at < 4°C for cold stabilisation for > 30<br />

days. The w<strong>in</strong>e was filtered <strong>in</strong>to 375 ml glass bottles with cork<br />

closures.<br />

Dur<strong>in</strong>g red v<strong>in</strong>ification, the must was divided <strong>in</strong>to 4 replicate fermentations<br />

at each tox<strong>in</strong> level. Potassium metabisulphite was added to<br />

give 50 ppm SO 2 <strong>in</strong> the must, diammonium phosphate was added at<br />

0.5 g/l must, and tartaric acid was added to br<strong>in</strong>g the titratable acidity<br />

to 6.5 g/l. The yeast D254 (Lallemand, Toulouse, France) was rehydrated<br />

and added at approximately 0.3 g/l must. The cap was plunged<br />

2-3 times daily. The must was pressed after 4 days of fermentation at<br />

room temperature <strong>in</strong> 2002, and after 6 days of fermentation at approximately<br />

20°C <strong>in</strong> 2003. Fermentation was f<strong>in</strong>ished <strong>in</strong> bottles at room<br />

temperature. Dur<strong>in</strong>g the first rack<strong>in</strong>g, 50 ppm SO 2 was added, after

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