Molecular Plant Breeding Provisional Publishing
Molecular Plant Breeding 2012, Vol.3, No.4, 37
-
49
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48
settling tower among plates at the time of inoculation
and later on conidia were counted under microscope.
Culture plates were covered with lids and sealed with
sealing film and kept at 16
℃
in the dark for overnight.
After that these plates were transferred to infection
chambers where a temperature of 18
℃
and light to
dark period ratio of 16:8 hours were maintained for the
next 21 days. Fungus development was observed and
number with size of developing colonies was taken.
Acknowledgements
We are highly thankful to DAAD, Germany and HEC, Pakistan
for facilitating and funding the stay of a PhD student (1
st
Author)
to do this research work. We are also thankful to Dr Kerstin Flath,
of Plant Pathology and grassland Institute Kleinmachnow,
Germany for providing fungal isolates and technical help to do
the pathological analysis.
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