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