Biodiversity of Plant Pathogenic Fungi - Kerala Forest Research ...
Biodiversity of Plant Pathogenic Fungi - Kerala Forest Research ...
Biodiversity of Plant Pathogenic Fungi - Kerala Forest Research ...
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well as fructifications in culture medium, a freeze microtome (Minotome-Cryostat, IEC,<br />
USA) was also used. The sections <strong>of</strong> fructifications <strong>of</strong> various fungi were observed under<br />
Leitz Dialux –20 Microscope and photomicrographs were prepared. Identification <strong>of</strong> the<br />
fungi up to species level, as far as possible, was made based on their cultural and<br />
morphological characteristics. The fungal isolates which belong to possibly new taxa and<br />
hitherto unpublished were assigned species number as Sp.1, Sp.2, etc. for publication<br />
elsewhere. However, information on the cultural characteristics, morphological and<br />
pathological peculiarities are provided for all such fungi at appropriate places in the text.<br />
All the fungal isolates were pure cultured and assigned KFRI. Culture No. and<br />
maintained in the Microbial Culture Collection Facility at KFRI.<br />
<strong>Pathogenic</strong>ity trials<br />
<strong>Pathogenic</strong>ity <strong>of</strong> fungal isolates was tested using seedlings <strong>of</strong> the respective host plants<br />
raised in the glasshouse. As it is not practical to test all the fungi isolated to their<br />
respective host plants to establish the pathogenic status, only selected fungi (rarely<br />
encountered ones, new species and weak pathogens) were screened. <strong>Pathogenic</strong>ity <strong>of</strong> the<br />
fungal isolates to the respective hosts was tested by using 3-6 month-old seedlings and<br />
spraying conidial suspension (2 x 10 3 conidia/ml <strong>of</strong> sterile water) <strong>of</strong> the respective<br />
fungus. Three to five seedlings <strong>of</strong> the respective host plants were inoculated and the<br />
inoculated seedlings were incubated in humidity chamber (>90% r.h, 26 ± 2 0 C with 12 h<br />
dark and light period). Disease symptoms developed in the host plants were recorded and<br />
fungus was re-isolated from the diseased host tissues and pathogenicity <strong>of</strong> the respective<br />
fungal species confirmed.<br />
<strong>Biodiversity</strong> analyses<br />
Numerical data on pathogenic fungi obtained from representative study plots under each<br />
forest ecosystem were pooled and Species richness indices (Margalef’s index and<br />
Menhinick’s index), Species diversity indices (Simpson’s index and Shannon’s index)<br />
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