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Contents of 41(2) 2013 - acharya ng ranga agricultural university

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PARASHURAM and JAYARAME<br />

MATERIALS AND METHODS<br />

Heterosis for yield and its attributing traits<br />

Four lines were crossed to four testers in a<br />

line x tester mating design (Kempthorne, 1957) in<br />

kharif-2009, to generate hybrids by following hot water<br />

treatment (Rao and Rao, 1962) for emasculation then<br />

contact method for crossing (Ayyangar and Warrior,<br />

1934). Crossed seeds along with their parents were<br />

sown in nursery during rabi-2009. The hybrids were<br />

first identified in the nursery using purple plant<br />

pigmentation as marker. All the eight parents (4 lines<br />

and 4 testers) together with 16 crosses were evaluated<br />

during rabi-2009. The material was grown in a single<br />

row of 3 m length with a spacing of 30 x 10 cm in a<br />

randomized block design and replicated twice. The<br />

data were recorded on plant height, number of fingers<br />

per ear, number of productive tillers per plant, finger<br />

length, finger width, culm width, peduncle length,<br />

days to 50 per cent flowering, days to maturity, straw<br />

yield per plant, grain yield per plant and test weight<br />

on five randomly selected plants. The analysis of<br />

Randomised Block Design was carried out based on<br />

the methods described by Panse and Sukhatme<br />

(1967) and significance of heterosis was tested using<br />

simple‘t’ test at five per cent and one per cent level<br />

of significance. The magnitude of heterosis was<br />

estimated over mid parent and better parent (Singh<br />

and Chaudhary, 1985).<br />

Intra Spikelet Competition for Seed Size<br />

The material for this study comprised of<br />

mature spike/fingers of three varieties viz., HR 911,<br />

PR 2O2 and GPU 28. These varieties were grown<br />

both in field and pots in green house. Each spike<br />

was divided into three portions. The florets from 1/3 rd<br />

position of top, 1/3 rd of middle and 1/3 rd of bottom<br />

position of spike of each variety were taken<br />

separately. Approximately 100 spikelets from each<br />

portion were selected in all three varieties. In each<br />

finger there are about 70 spikelets, each spikelet<br />

having five to seven complete flowers. However, the<br />

experimental varieties having six florets from each<br />

spikelet from top to bottom of the spike. The positions<br />

of florets in each spikelet were numbered (only six<br />

florets hence numbered from one to six) and the<br />

seeds of particular position were taken out which were<br />

numbered from one to six to a particular bowl which<br />

were also numbered as one to six. Thousand grain<br />

weights of separately collected floret wise seeds of<br />

three different positions was weighed and compared.<br />

Analysis of variance for three factorial Completely<br />

Randomized Design for floret wise seed weight of<br />

three portions of three different varieties was<br />

constructed. The varieties were considered as main<br />

factors. Sub factors were portions (3), because each<br />

variety has been divided into three portions and subsub<br />

factors were 6, because each spikelet consists<br />

of six florets, for which competition between florets<br />

was studied.<br />

RESULTS AND DISCUSSION<br />

Heterosis for yield and related traits<br />

The analysis of variance revealed significant<br />

differences among the parents as well as crosses<br />

for all the traits. Higher level of significance in the<br />

variance of parents vs hybrids for all the characters<br />

clearly indicated the existence of significant level of<br />

average heterosis in the hybrids (Table 2). Non<br />

additive gene action was noticed for all the characters<br />

studied. The results support the findings of<br />

Tamilcovane (1994), Madhusudhan et al. (1995) and<br />

Patel (1994).<br />

Among 16 hybrids developed, per cent<br />

heterosis over mid parent and better parent was<br />

negatively significant in most of the hybrids except<br />

in crosses, GE 6216 x GPU 69 and GE 6216 x GE<br />

5095 for days to 50 per cent flowering and except<br />

GE 6216 x GPU 69 and GE 4906 x GE 5095 for days<br />

to maturity suggesting the involvement of dominant<br />

gene action with negative effects (Table 3). The earlier<br />

reports suggest that early types can be obtained from<br />

crosses which record negative heterosis. Similar<br />

results were obtained by Konstantinov and Linnik<br />

(1985) and Ramesh (1990) in proso millet. Significant<br />

level of heterosis over mid parent and better parent<br />

have been observed for the characters like plant<br />

height, number of productive tillers per plant, straw<br />

yield per plant and grain yield per plant.<br />

From this study, it can be concluded that<br />

the non additive gene action favouring hybridization<br />

to some extent and the crosses, GE 4596 x L 5 and<br />

GE 4596 x GPU 69 are the best crosses for grain<br />

yield and most of the yield contributing characters.<br />

34

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