from three fungal species which were the most effective in both
experiments were selected for development of bioformulations.
The fungal isolates were first grown on PDA culture medium to
verify their purity and were incubated for three weeks for spore
production. The spores in the Petri plates were washed out by
adding 10 ml of distilled water to each plate. A hemocytometer was
used to count the spores and then the concentration of the suspension
was adjusted to 106 spore ml1.