Both spontaneous and induced types of asynapsis and desynapsis have been reported in a number of plant species (Beadle 1933, Prakken 1943, Li et al. 1945, Soost 1951, Ross et al. 1960, Chao et al. 1960, Dyck and Rajhathy 1965, Riley and Law 1965, Chennaveeraiah and Krishnappa 1968, Jauhar and Singh 1969, Sjodin 1970, Sharma and Reinbergs 1974, Srivastava 1974, Palmer 1974, Sahu et al. 1981. In most of the cases they have been governed by genes. Some asynaptic and de synaptic mutants were isolated from DES treated populations of barley. The present paper describes the cytology and genetics of these mutants.
Materials and methodsDuring study of chemical mutagenesis in barley (Hordeum vulgare L.) several partially sterile (PS) plants were isolated from M2 generation of the seeds of cultivar DL 36 treated with 0.3 per cent aqueous solution of diethyl sulphate (DES). Sporocytes were collected in 3:1 alcohol-acetic acid solution and preserved in 70 per cent ethanol. Slides were prepared in 2 per cent aceto-propiono-carmine. Meiotic study showed that one of the PS plants was asynaptic and three plants were desynaptic mutants. Next year (in M3) these mutants were crossed with the mother variety DL 36 reciprocally. Data on F2 segregation were recorded and x2-test was applied for inheritance of asynapsis and desynapsis.
ResultsSterility and seed set Mutants were highly sterile. Table 1 shows that the asynaptic plant DM 11-10 produced 97.0 per cent sterile pollen grains. Number of seeds per spike in this mutant ranged from 0 to 4 and average seed set was 3.5 per cent. In desynaptic mutants DM 1-15, DM 6-6 and DM 16-7, pollen sterility was 90.5, 37.8 and 35.0 per cent, respectively. Average seed set was 6.5, 68.0 and 66.3 per cent in the re spective desynaptic mutants.
CytologyProphase I: There was absence of chromosome pairing in asynaptic plant DM 11-10. All the PMCs of this plant showed invariably the presence of 14 uni valents at pachytene, diplotene and diakinesis (Figs. la,b). In the desynaptic plants,