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(shorl stature), and 18.6 x 10" (potato led character) were observed in regenerated plants<br />

while lrequencies d only 0.6 x 10'' for male sterility and 1.7 x 10' for early ripening was<br />

observed from EMS treatments. From inheritance studies male sterility and shot stature<br />

appeared to behave as single gene recessive mutank potato leaf character appeared to be<br />

in a homozygous state; and resistance was controlled by a single dominant gene.<br />

Novak et al. (1988) compared gamma ray induced and tissue culture induced mutations in<br />

plants derived from zygotic embryos. They observed a greater frequency of variation In tiwe<br />

culture induced than in irradiated or Irradiated followed by in vitro regeneration treaiments.<br />

Inadidion followed by in vitro regeneration produced chlorophyll variations of 2.07% at 5 Gray<br />

units (Gy) and 2.23% at 10 Gy, tissue culture 1.94%, and irradiation 0.22% at 5 Gy and 0.24%<br />

at 10 Gy. 14.25% and 9.87% of the plants regenerated in vitro after exposure to 5 Gy and 10<br />

Gy respectively showed morphological variations. Irradiated material gave 3.4390 at 5 Gy and<br />

2.77% at I0 Gy, and tissue culture alone gave 5.39% of morphological variants. Early flowering<br />

variants were observed at 0.42% and 0.07% frequency when subjected to 5 and 10 Gy d<br />

irrcdiation; 0.5% in tlssue cultured plants; 2.89% and4.1446 in regenerated plantsafter exposure<br />

to 5 and 10 Gy respectively. Neg~itiu et al., (1984) extensively reviewed mutagenesis d<br />

protoplasts and the selection of biochemical mutants.<br />

All reporls agree that somaclonal variation has produced an order of magnitude grecrter<br />

numbers of variants than EMS or irradiatlon, although the two kinds of treatments may or may<br />

not generate the same spectrum ol mutations.

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