A simple technique was developed for purifying fungal cultures contaminated
with bacteria and mites. It was based on the observation that the growth o
f bacteria and movement of mites were confined to the upper surface of the
agar. A culture contaminated with bacteria and mites was transferred to a p
iece of clean paper with the upper surface facing down. Small thin pieces (
approximately 3 mm x 3 mm x 0.5 mm) of agar were removed from the exposed s
urface and transferred to a V-8 agar plate. Colonies that developed from th
ese agar pieces were free from bacteria and mites.