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Estimates of gene action for yield and its components in bread wheat Triticum aestivum L.

In order to study gene action for yield and its components using 8 × 8 diallel crosses excluding reciprocals during 2013/2014 and 2014/2015 growing seasons at Tag El-Ezz Research Station, Dakahlia Governorate, the genotypes were Sides 12, Gemmiza 11, Maser 1, Maser 2, Shandaweel 1, Giza 168, Sakha 93, and Sakha 94. Results revealed that both additive (D) and dominance (H1 and H2) genetic variance were significant for the all studied characters, indicating the importance of additive and dominance gene effects in controlling these characters. The dominance genetic variance was higher in the magnitude as compared to additive one, resulting in (H1/D)0.5 exceeding than more unity for all studied characters except spike density and number of tillers/plant. The “F” values which refer to the covariance of additive and dominance gene effects in the parents revealed positive and significant for flag leaf length and flag leaf area, extrusion length, number of tillers/plant number of spikes/plant, number of grains/spike and 1000- grain weight, indicating that dominant alleles were more frequent than the recessive ones in the parents for this character, while negative “F’ value for remaining characters indicated excess of recessive alleles among parents. The overall dominance effects of heterozygous loci h2, indicated directional dominance for heading date, flag leaf length, flag leaf area, spike length, extrusion length, spike density, grain yield/spike, number of tillers/plant number of spikes/plant, number of grains/ spike and grain yield/plant. Proportion of genes with positive and negative effects in the parent (H2/4H1) was deviated from 0.25 for all studied characters Heritability in narrow sense was moderate (0.369) for grain yield/plant.

In order to study gene action for yield and its components using 8 × 8 diallel crosses excluding reciprocals during 2013/2014 and 2014/2015 growing seasons at Tag El-Ezz Research Station, Dakahlia Governorate, the genotypes were Sides 12, Gemmiza 11, Maser 1, Maser 2, Shandaweel 1, Giza 168, Sakha 93, and Sakha 94. Results revealed that both additive (D) and dominance (H1 and H2) genetic variance were significant for the all studied characters, indicating the importance of additive and dominance gene effects in controlling these characters. The dominance genetic variance was higher in the magnitude as compared to additive one, resulting in (H1/D)0.5 exceeding than more unity for all studied characters except spike density and number of tillers/plant. The “F” values which refer to the covariance of additive and dominance gene effects in the parents revealed positive and significant for flag leaf length and flag leaf area, extrusion length, number of tillers/plant number of spikes/plant, number of grains/spike and 1000- grain weight, indicating that dominant alleles were more frequent than the recessive ones in the parents for this character, while negative “F’ value for remaining characters indicated excess of recessive alleles among parents. The overall dominance effects of heterozygous loci h2, indicated directional dominance for heading date, flag leaf length, flag leaf area, spike length, extrusion length, spike density, grain yield/spike, number of tillers/plant number of spikes/plant, number of grains/ spike and grain yield/plant. Proportion of genes with positive and negative effects in the parent (H2/4H1) was deviated from 0.25 for all studied characters Heritability in narrow sense was moderate (0.369) for grain yield/plant.

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Int. J. Agri. Agri. R.<br />

The " F " values which refer to the covariance <strong>of</strong><br />

additive <strong>and</strong> dom<strong>in</strong>ance <strong>gene</strong> effects <strong>in</strong> the parents<br />

revealed positive <strong>and</strong> significant <strong>for</strong> extrusion length,<br />

<strong>in</strong>dicat<strong>in</strong>g that dom<strong>in</strong>ant alleles were more frequent<br />

than the recessive ones <strong>in</strong> the parents <strong>for</strong> this<br />

character. The overall dom<strong>in</strong>ance effects <strong>of</strong><br />

heterozygous loci h 2 , <strong>in</strong>dicated directional dom<strong>in</strong>ance<br />

<strong>for</strong> all studied characters except number <strong>of</strong><br />

spikelet's/spike. Proportion <strong>of</strong> <strong>gene</strong>s with positive <strong>and</strong><br />

negative effects <strong>in</strong> the parent (H2/4H1) was deviated<br />

from 0.25 <strong>in</strong> the ma<strong>in</strong> spike characters. The ratio <strong>of</strong><br />

dom<strong>in</strong>ance to recessive alleles (KD /KR) <strong>in</strong> the parents<br />

which was < 1 <strong>for</strong> the ma<strong>in</strong> spike characters except<br />

spike density; showed an excess <strong>of</strong> decreas<strong>in</strong>g alleles<br />

among parental genotypes. Heritability <strong>in</strong> broad<br />

sense ranged from 0.505 (spike density) to<br />

0.843(extrusion length) <strong>for</strong> all the studied characters.<br />

Heritability values <strong>in</strong> narrow sense (Tn) found to be<br />

high (>50 %) <strong>for</strong> spike length (0.682), number <strong>of</strong><br />

spikelets/spike (0.638), <strong>and</strong> spike gra<strong>in</strong> weight<br />

(0.601), Thus phenotypic selections was effective <strong>in</strong><br />

improv<strong>in</strong>g these character.<br />

<strong>and</strong> <strong>in</strong>dicated that both additive (D) <strong>and</strong> dom<strong>in</strong>ance<br />

(H1 <strong>and</strong> H2) <strong>gene</strong>tic variance were significant <strong>for</strong> the<br />

all studied characters, <strong>in</strong>dicat<strong>in</strong>g the importance <strong>of</strong><br />

additive <strong>and</strong> dom<strong>in</strong>ance <strong>gene</strong> effects <strong>in</strong> controll<strong>in</strong>g<br />

these characters. The dom<strong>in</strong>ance <strong>gene</strong>tic variance was<br />

higher <strong>in</strong> the magnitude as camporees to additive one,<br />

result<strong>in</strong>g <strong>in</strong> (H1/D) 0.5 exceed<strong>in</strong>g than more unity <strong>for</strong>,<br />

all studied characters except number <strong>of</strong> tillers/plant.<br />

Us<strong>in</strong>g The diallel crosses among n<strong>in</strong>e <strong>bread</strong> <strong>wheat</strong><br />

cultivars <strong>in</strong> two sow<strong>in</strong>g dates <strong>for</strong> gra<strong>in</strong> <strong>yield</strong>/plant <strong>and</strong><br />

<strong>yield</strong> <strong>components</strong> i.e. number <strong>of</strong> spikes/plant,<br />

number <strong>of</strong> gra<strong>in</strong>s/pike as well as 1000-gra<strong>in</strong> weight.<br />

Resulted showed that the importance <strong>of</strong> additive <strong>gene</strong><br />

effects <strong>in</strong> controll<strong>in</strong>g these characters. The dom<strong>in</strong>ance<br />

<strong>gene</strong> effects were significant <strong>for</strong> number <strong>of</strong><br />

gra<strong>in</strong>s/spike <strong>in</strong> both sow<strong>in</strong>g dates <strong>and</strong> pooled data as<br />

well as 1000-gra<strong>in</strong> weight <strong>in</strong> late sow<strong>in</strong>g. But, additive<br />

<strong>gene</strong> effects were significant <strong>in</strong> pooled data <strong>for</strong> 1000-<br />

gra<strong>in</strong> weight. (Ja<strong>in</strong> <strong>and</strong> S<strong>in</strong>gh (1976), Awaad (1996)<br />

<strong>and</strong> Salama (2000 a), <strong>for</strong> number <strong>of</strong> spikes/plant,<br />

Dasgupta <strong>and</strong> Mondal (1988), Al Kaddoussi (1996),<br />

Salama (2000a), J<strong>in</strong>bao et al. (2014), Naseem et al.<br />

(2015) <strong>and</strong> Ahmed et al. (2015) <strong>for</strong> number <strong>of</strong><br />

Yield <strong>and</strong> <strong>yield</strong> <strong>components</strong><br />

gra<strong>in</strong>s/spike <strong>and</strong> 1000-gra<strong>in</strong> weight).<br />

When us<strong>in</strong>g second degree statistics Hayman (1954),<br />

various <strong>gene</strong>tic parameters were computed Table (4)<br />

Table 4. Genetic <strong>components</strong> together with derived parameters <strong>for</strong> Yield <strong>and</strong> <strong>yield</strong> <strong>components</strong>.<br />

Number <strong>of</strong><br />

Number <strong>of</strong><br />

Number <strong>of</strong><br />

1000-gra<strong>in</strong> weight<br />

Gra<strong>in</strong><br />

tillers/plant<br />

spikes/plant<br />

gra<strong>in</strong>s/spikes<br />

<strong>yield</strong>/plant<br />

D 0.216**±0.029 0.107**±0.028 0.982**±0.007 0.916**±0.141 0.310**±0.114<br />

H₁ 0.152*±0.073 0.341**±0.071 3.156**±1.851 3.988**±1.00 7.852**±0.636<br />

H₂ 0.138**±0.043 0.272**±0.036 2.981*±1.432 2.532**±0.491 4.814**±1.431<br />

F 0.160**±0.068 0.162**±0.056 1.063**±1.025 1.410**±0.151 1.521±1.528<br />

h² 1.021**±0.041 1.750**±0.022 0.416±1.731 3.061**±0.245 8.173**±0.151<br />

E 0.130**±0.015 0.141**±0.010 1.568**±0.231 1.853**±0.126 1.991**±0.542<br />

(H₁ / D)½ 0.839 1.785 1.792 2.086 5.033<br />

H₂ / 4H₁ 0.226 0.199 0.236 0.158 0.2077<br />

KD / KR 2.584 2.473 3.3511 2.169 1.972<br />

מT<br />

0.729 0.472 0.259 0.206 0.369 Tь 0.801 0.932 0.611 0.477 0.750<br />

The " F " values which refer to the covariance <strong>of</strong><br />

additive <strong>and</strong> dom<strong>in</strong>ance <strong>gene</strong> effects <strong>in</strong> the parents<br />

revealed positive <strong>and</strong> significant <strong>for</strong> all studied<br />

characters except gra<strong>in</strong> <strong>yield</strong> / plant, <strong>in</strong>dicat<strong>in</strong>g that<br />

dom<strong>in</strong>ant alleles were more frequent than the<br />

K<strong>and</strong>il et al.<br />

recessive ones <strong>in</strong> the parents <strong>for</strong> this character. The<br />

overall dom<strong>in</strong>ance effects <strong>of</strong> heterozygous loci h 2 ,<br />

<strong>in</strong>dicated directional dom<strong>in</strong>ance <strong>for</strong> all <strong>yield</strong><br />

characters except number <strong>of</strong> gra<strong>in</strong>s/spike. The value<br />

<strong>of</strong> (H2/4H1) was deviated from 0.25 <strong>in</strong> <strong>yield</strong><br />

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