Greener Journal of Plant Breeding and Crop Science

Vol. 8(1), pp. 06-12, 2020

ISSN: 2354-2292

Copyright ©2020, the copyright of this article is retained by the author(s)

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Genetic variability of yield and yield related traits in bread wheat (Triticum aestivum. L) Genotypes under high temperature condition

 

 

Tadiyos Bayisa Serbesa1*; Mihratu Amanuel Kitil2

 

 

1 Tadiyos Bayisa Serbesa (Associate Researcher), Ethiopian Institute of Agricultural Research, Werer Agricultural Research Center, Werer, Ethiopia. E-mail:bayisatadiyos@gmail.com. Phone: +251913911673

2 Mihratu Amanuel Kitil (Researcher-I), Ethiopian Institute of Agricultural Research, Werer Agricultural Research Center, Werer, Ethiopia. E-mail: mihratuamnuel@gmail.com; Phone: +251911005935

 

 

 

ARTICLE INFO

ABSTRACT

 

Article No.: 110319181

Type: Research

 

 

Information on the extent and pattern of genetic variability of bread wheat genotypes under high temperature stress condition is limited. The present study was conducted with the objective of assessing the presence of genetic variability in 36 bread wheat genotypes under high temperature stress condition for yield and yield related traits. The genotypes were evaluated using Triple Lattice Design with three replications at Werer agricultural research center, Afar region in 2017.  The data generated from the experiment were subjected to analysis of variance and genetic analyses. The analysis of variances of bread wheat genotypes evaluated for 11 traits revealed highly significant difference between the genotypes for most traits except days to emergence. Genotypic coefficient of variation (GCV) and phenotypic coefficient of variation (PCV) values were high for grain yield/ha, biomass yield/ha and harvest index. Also, moderate values for both GCV and PCV were obtained for traits. The magnitude of PCV values higher than GCV which indicates the degree of influence of environment over genotypic effect. The value of heritability in broad sense ranged from 66.72% for Number of kernel per spike to 97.79 for days to heading while genetic advance as percent of mean was ranged from 16.07(number of spikelet per spike) to 41.20 yield kg/ha. High heritability accompanied with high genetic advance as percent of the mean was recorded for days to heading, plant height, spike length, biomass, thousand kernel weights and harvest index which revealed traits was simply inherited.  Hence, from the current results it has been observed adequate existence of variability for most of the traits in the studied genotypes and these genotypes could be exploited in future bread wheat breeding for high temperature stress condition.

 

Accepted:  19/11/2019

Published: 07/05/2020

 

*Corresponding Author

Tadiyos Bayisa Serbesa

E-mail: bayisatadiyos@ gmail.com

Phone: +251913911673

 

Keywords: Bread wheat; Genetic Advance; Heritability; Variability

 

 

 

 

 

 


INTRODUCTION

 

Wheat (Triticum aestivum L.) is one of the most important cereal crop world-wide that grown in many areas and major staple crops with about 751.4 million tons’ annual production (USDA, 2017).  In Sub-Saharan Africa (SSA), wheat is grown by millions of resource poor smallholder farmers predominantly under rain-fed conditions. The consumption of wheat also is increasing by approximately 650,000,000 tons per year in SSA (Mason et al., 2012). Similarly, wheat is the most important crop in Ethiopia and ranked 4th in area (13.38%) and grain production (15.17%) of total grain crops next to Tef, Maize and Sorghum which has resulted to increase in a production mainly by smallholder farmers using rain-fed based production system and used mainly for food (CSA, 2018).  Both bread wheat (Triticum aestivum L. em. Thell) and durum wheat (Triticum turgidum L. subsp.durum.) are the two most important wheat species which are mainly grown in the country (Amsal, 2001). The consumption of wheat in our country is increasing with increasing food variety. There are seven bread wheat varieties have been officially released for irrigated lowland areas of Ethiopia (Desta et al., 2017 and Mihratu et al., 2019) which is in a good progress. The released bread wheat varieties at Middle and Lower-Awash areas are only for off season growing from October to February. However, for the main growing season that runs from May to September which is characterized by high temperature, there are no heat adaptable varieties. The generation of adaptable varieties largely depends on the availability of desirable genetic variability for important traits (Pratap et al., 2012). Success in crop breeding program depends on the magnitude of genetic variability present in a material and the extent to which the desirable characters are heritable (Kahrizi et al., 2010).

 

Estimation of the magnitude of variation with in genotype for important plant attributes will enable breeders to exploit genetic variability more efficiently. This is due to the serious role of genetic variability in determining the amount of progress to be made by selection.  However, the existence of variation alone in the population is not sufficient to improve desirable traits and also high heritability is needed to have better opportunity to select directly for the traits of interest which delivers information about the extent to which a specific trait can be transmitted to the successive generation and estimates of genetic advances are important initial steps in any breeding programs they provide information about effective selection. High genetic advance coupled with high heritability estimates offer a most suitable condition for selection (Larik and Joshi, 2004). Therefore, selection is an important part by which genotypes with high productivity in a given environment could be developed and it will be effective when there is a significant amount of variability among the breeding materials (Sumanth et al., 2017).  The available variability can be measured using genotypic and phenotypic coefficient variation which used to partition genetic and environmental variance (Oniya et al., 2017; Pratap et al., 2012, ). Therefore, the current study was carried out with the objective of assessing the genetic variability, genetic advance and heritability between yield and yield related traits of bread wheat genotypes under high temperature stress environment.

 

 

MATERIALS AND METHODS

 

The experiment was conducted at Werer Agricultural Research Center (WARC) during main cropping season in 2017. WARC is located at middle Awash of Afar National Regional state at a distance of 278 km from Addis Ababa to the east direction near to the main road from Addis to Djibouti at altitude of 740 m above sea level. The center is located at 90 16’ 8” N latitude and 400 9’41”E longitudes. The area has a mean maximum and minimum annual temperature of 340c and 190c and monthly temperature of 38.060c and 21.060c during main season, respectively. The precipitation in study area is characterized by unpredictable and uneven distribution with annual average rainfall about 571 mm which is not sufficient for crop production. The main irrigation water source is from Awash River. The soil in the testing field of Werer is predominantly Fluvisols (Wendmagegn and Abere, 2012) while vertisol are the second dominant soil that occupies about 30% of the total area. The experiment was carried out in Triple Lattice Design consisted of 36 entries sown in three replications on 9 m2 plot size which accommodated five ridge at 0.6m spacing with two rows each with net harvestable plot area 7.2 m2. The planting date was June 24, 2017. Seeds were sown on rows with manual drilling at a rate of 100 kg ha-1 basis. Fertilizer was applied at a rate of 50 kg ha-1 P205 in DAP form once at sowing time and 100kg of N (Urea) ha-1 applied in split; half at seedling stage and the remaining 50% at booting stages. The irrigation water was applied at every 10days interval using furrow method and agronomic activities were applied uniformly for each treatment.


 

 

Table 1. The evaluated bread wheat genotypes are listed below.

Trt

 

 Cross/Pedigree

Origin

1

 

MILAN/KAUZ//PRINIA/3/BAV92/5/TRAP#1/BOW

CIMMYT/ICARDA

2

 

RL6043/4*NAC//PASTOR/3/BAV92/4/ATTILA/BAV92

CIMMYT/ICARDA

3

 

ESDA/KKTS

CIMMYT/ICARDA

4

 

ATTILA*2/PBW65//TAM200/TUI

CIMMYT/ICARDA

5

 

ATTILA/3*BCN//BAV92/3/TILHI/4/SHA7/VEE

CIMMYT/ICARDA

6

 

THB/KEA//PF85487/3/DUCULA/4/WBLL1*2/TUKURU

CIMMYT/ICARDA

7

 

ATTILA*2//CHIL/BUC*2/3/KUKUNA

CIMMYT/ICARDA

8

 

ATTILA*2/PBW65//KACHU

CIMMYT/ICARDA

9

 

FRET2/KUKUNA//FRET2/3/PARUS/5/FRET2*2/4/SNI

CIMMYT/ICARDA

10

 

NAC/TH.AC//3*PVN/3/MIRLO/BUC/4/2*PASTOR

CIMMYT/ICARDA

11

 

ROLF07/4/BOW/NKT//CBRD/3/CBRD/5/FRET2

CIMMYT/ICARDA

12

 

MUNAL#1/FRANCOLIN#1

CIMMYT/ICARDA

13

 

WBLL1*2/BRAMBLING/4/BABAX/LR42//BABAX

CIMMYT/ICARDA

14

 

BECARD/AKURI

CIMMYT/ICARDA

15

 

BAJ#1/AKURI

CIMMYT/ICARDA

16

 

ATTILA*2PBW65//MUU#1/3/FRANCOLIN#1

CIMMYT/ICARDA

17

 

WAXWING*2/HEILO

CIMMYT/ICARDA

18

 

BOHAINE

CIMMYT/ICARDA

19

 

SERI.IBKAUZ/HEVO/3/AMAD/4/ESD/SHWA/BCN

CIMMYT/ICARDA

20

 

FERROUG-2/FOW-2

CIMMYT/ICARDA

21

 

SOKOLL//PBW343*2/KUKUNA/3/ATTILA/PASTOR

CIMMYT/ICARDA

22

 

QUATU3//MILAN/AMSEL

CIMMYT/ICARDA

23

 

ATTILA*2/PBW65*2/4/CROC1/AE.SQUARROSA(205)

CIMMYT/ICARDA

24

 

ATTILA*2/PB W65*2//W485/HD29

CIMMYT/ICARDA

25

 

SAUAL/3/ACHTAR*3//KANZ/KS85.8.4/4/SAU

CIMMYT/ICARDA

26

 

ALTAR84/AE.SQUARROSA (221)//3*BORL95

CIMMYT/ICARDA

27

 

TACHUPETOF2001/6/OASIS/5*BORL95/5/CNDO/R143

CIMMYT/ICARDA

28

 

KAUZ/RAYON/3/N5732/HER//CASKOR

CIMMYT/ICARDA

29

 

KSAYONGENARO81//TEVEE.I/./4/CHEN/AEGILOPS

SQUARROSA (TAUS)//BCN/3/KAUZ

CIMMYT/ICARDA

30

 

IMAM

CIMMYT/ICARDA

31

 

SHUHA-8/DUCULA

CIMMYT/ICARDA

32

 

TUKURU//BAV92/RAYON/3/FRNCLN

CIMMYT/ICARDA

33

 

TACUPETOF2001*2/BRAMBLING//WBLL1*2/BRANBLING

CIMMYT/ICARDA

34

 

WAXWING/4/BL1496/MILAN/3/CROC-1/AE.SQUA9205)//kauz/5/frncln

CIMMYT/ICARDA

35

 

WAXWING/2*ROLF07  

CIMMYT/ICARDA

36

 

SAMAR-13/PASTOR-1

CIMMYT/ICARDA

CIMMYT=International Maize and Wheat Improvement Center, ICARDA=International Center for Agricultural Research in the Dry Land Areas.

 

 


Observations were recorded for Days to emergence, Days to heading, Days to maturity, Plant height, Spike length, 1000 grain weight, Number of spikelet /spike, Number of seed/spike, Grain yield, Biomass yield and Harvest index. The recorded data were subjected to analysis of variance (ANOVA) as suggested by Gomez and Gomez (1984) using SAS Software (Version 9.0). Different genetic parameters including genotypic variance (σ2g), phenotypic variance (σ2p), phenotypic coefficient of variation (PCV) and genotypic coefficient of variation (GCV) were estimated by using the formula adopted from Burton and De vane (1953) and Johnson et al.,(1955a and 1955b).

 

Phenotypic variance (σ2p) = σ2g + σ2e

 

Genotypic variance σ2g=MSG-MSe

                                          r

 

 Phenotypic Coefficient of Variation PCV= (√σ2p / grand mean) *100

Genotypic Coefficient of Variation GCV= (√σ2g / grand mean) *100

 

H2 = σ2g / σ2p *100 

 

Where:

 

σ2p = phenotypic variance

 σ2e = Environmental (error) variance  

σ2g= genotypic variance

MSg = mean square due to genotypes.

MSe= environmental variance (error mean square)

r = number of replication

H2= heritability 

 

Genetic advance (GA) for each character was computed using the formula adopted from Johnson et al. (1955a) and Allard (1960). 

 

 

Where:  σp = Phenotypic standard deviation 

                  

k= selection differential (at 5%   selection intensity, k=2.06)

X=Grand mean

 

 

RESULTS AND DISCUSSIONS 

 

Analysis of Variance

 

Analysis of variances of 36 bread wheat genotypes evaluated for 11 traits revealed that highly significant (P≤ 0.01) difference among genotypes for all traits except for days to emergence (Table 2). The significant difference among genotypes for the traits indicated the presence of a considerable amount of variability among genotypes which is an essential to the study of plant breeders for enhancement of these traits through breeding. The mean square due to replication showed highly significant difference for biomass yield and significant difference for days to emergence, spike length and grain yield which indicate the heterogeneity present in the field.


 

Table 2.  The Analysis of Variance (ANOVA) for different sources of variations and the corresponding CV in percentage for eleven traits.

 Traits

 

 Mean Squares

 

 

 CV%

 

Replication

Block(group)

Genotype

Error

 

 

  d.f=2

d.f=15

d.f=35

d.f=55

 

DE

2.23*

0.60

0.62ns

0.64

12.07

DH

2.12

2.85

108.46**

2.94

3.16

DM

8.08

5.82

117.93**

7.23

3.09

PH

75.58

29.85

124.20**

27.35

8.50

SL

1.638*

0.83*

2.77**

0.41

8.06

NSSP

2.36

0.49

4.10**

0.86

6.21

NKSP

26.96

22.56

59.12**

18.94

12.15

BY

11287194.60**

1493156.10

4950469.40**

1024604.50

14.62

TKW

6.38

4.13

26.40**

4.08

7.30

GY

736350.08*

122589.13

482329.00**

105636.47

16.76

HI

5.11

9.22

77.84**

12.43

12.32

 

*, ** and ns,  significant at 5%, 1%   probability level and non-significant, respectively.

Where:  d.f= degree of freedom, CV= coefficient of variation, DE=days to emergence, DH=days to heading, DM= days to maturity, PH= plant height, SL= spike length, NSSP= number of spikelet per spike, NKSP=number of kernels per spike, BY=biomass yield kg/ha, TKW= thousands kernel weight, GY=grain yield kg/ha, HI= harvest index. 

 

 


Genotypic and Phenotypic Coefficient of Variation

 

Values of genotypic coefficient of variation (GCV) and phenotypic coefficient of variation (PCV) were calculated and presented in table 3. According to Sivasubramanian and Madhavamenon (1973), GCV and PCV can be categorized as high (>20%), moderate (10-20%) and low (<10%). Based on this category, PCV values were high for grain yield, biomass and harvest index. Similar findings also reported by Kumer et al. (2013) and Bilgin et al. (2011) that show high PCV for grain yield and harvest index. Moderate values for both GCV and PCV were obtained for days to heading (12.08, 12.48), spike length (11.67, 14.24), number of kernel per spike (10.13, 16.01), biomass/ha (18.25, 23.47), thousand kernel weight (10.32, 12.65), yield/ha (18.88, 25.39) and harvest index (17.04, 20.83) indicated these traits was under control of additive genes and modified selection would be effective for improvement of these traits. The finding of this study is  in agreement with results reported by Kumar et al. (2013) and Ali et al. (2008) for plant height and Mohammed et al. (2011) for plant height and kernels per spike that moderate values for both genotypic coefficient of variation (GCV) and phenotypic coefficient of variation (PCV) were recorded.

 

Low genotypic coefficient of variation (GCV) and phenotypic coefficient of variation (PCV) were estimated for days to maturity (7.89, 8.45) and number of spikelets per spike (7.39, 9.47) respectively which revealed that these traits are highly influenced by environmental factors and difficult for manipulating through direct selection. These results were supported by the findings of Bhushan et al. (2013) and Mohammad et al. (2011) for days to maturity and current results was at par with findings of Ashfaq et al., (2014) and Haq et al., (2016). Generally, the observation of higher PCV values than GCV values might suggest greater role of environment than genotype effect on the expression of the traits. Hence, the magnitude of difference between PCV and GCV values indicates the degree of influence of environment over genotypic effect.

 

Heritability and Genetic Advance

 

Although the genotypic coefficient of variation showed the extent of genetic variability present in the genotypes for various traits, it does not provide full scope to assess the variation that is heritable. The genotypic coefficient of variation along with heritability estimates provide reliable estimate of the amount of genetic advance to be expected through phenotypic selection (Burton, 1952). The estimate of genetic advance is more useful as a selection tool when considered jointly with heritability estimates (Johnson et al., 1955a).

 

Heritability in broad sense ranged from 66.72% for Number of kernel per spike to 97.79 for days to heading while genetic advance as percent of mean was ranged from 16.07(number of spikelets per spike) to 41.20(yield kg/ha) (Table 4). Pramoda and Gangaprasad (2007) generally classified heritability estimates as low (<40%), medium (40-59%), moderately high (60-79%) and very high (80-100%). Hence, high heritability were obtained for  biomass yield (82.13%), number of spikelet’s per spike (82.37%), thousand kernel weight (85.66%), harvest index (85.86%), spike length (85.99%), days to maturity (95.34%) and days to heading (97.79%). Moderately high heritability was recorded for number of kernel per spike (66.72), yield/ha (78.77) and plant height (79.44). This results in agreement with the finding of Awale et al. (2013) who reported heritability estimates were very high for days to heading (89.08%) and moderately high heritable for plant height (74.04%). Similarly Kalimullah et al. (2012) also showed high heritability estimates for thousand seed weight (98.11%). Selection based on phenotypic performance would be effective for trait that show high heritability, as indicated by Tabbal and Fraihat, (2012); Kaddem et al., (2014) and Navil et al., (2014). Moderate genetic advance as percent of mean was obtained for number of spikelet per spike (16.07%) and days to maturity (16.60%). Therefore, simple selection would be not effective for improvement and modified selection would be playing an important role in enhancement of these traits. Taken together high heritability accompanied with high genetic advance as percent of the mean was recorded for days to heading, plant height, spike length, biomass yield, thousand kernel weight and harvest index which imply that phenotypic selection to improve these traits.


 

 

 Table 3. Estimation of variability components (genotypic and phenotypic variances and coefficient of variations) for traits studied in bread wheat genotypes.   

 

 

 

 

 

 

 

 

Traits

σ2g

σ2p

 

σ2e

 

GCV (%)

 

PCV (%)

DH

42.96

45.87

 

2.91

 

12.08

 

12.48

 

DM

47.26

54.19

 

6.93

 

7.89

 

8.45

 

PH

35.90

63.79

 

27.88

 

9.73

 

12.97

 

SL

0.87

1.29

 

0.42

 

11.67

 

14.24

 

NSSP

1.22

2.00

 

0.78

 

7.39

 

9.47

 

NKSP

13.17

32.88

 

19.71

 

10.13

 

16.01

 

BY

1596637.68

2638815.50

 

1042177.82

 

18.25

 

23.47

 

TKW

8.14

12.23

 

4.09

 

10.32

 

12.65

 

YLD

134089.78

242532.32

 

108442.54

 

18.88

 

25.39

 

HI

        23.77

            35.50

 

11.74

 

17.04

 

20.83

 

σ2g, σ2p and σ2e = genotypic, phenotypic and environmental variances, respectively. GCV (%) and PCV (%) = genotypic and phenotypic coefficient of variations, respectively. DH=days to heading, DM= days to maturity, PH= plant height, SL= spike length, NSSP= number of spikelet’s per spike, NKSP=No of kernel per spike, BMS=biomass yield kg/ha, TKW= thousands kernel weight, YLD=yield kg/ha, HI= harvest index.


 

 

Table 4. Estimation of heritability and genetic advance for ten traits studied in bread wheat genotypes.

 

 

 

 

 

 

 

 

Traits

 

GA

 

GAM (%)

 

H2 (%)

 

 

DH

 

13.64

 

25.15

 

97.79

 

 

DM

 

14.46

 

16.60

 

95.34

 

 

PH

 

13.07

 

21.23

 

79.44

 

 

SL

 

2.01

 

25.23

 

85.99

 

 

NSSP

 

2.40

 

16.07

 

82.37

 

 

NKSP

 

7.88

 

22.01

 

66.72

 

 

BY

 

2748.37

 

39.70

 

82.13

 

 

TKW

 

6.17

 

22.32

 

85.66

 

 

YLD

 

799.09

 

41.20

 

78.77

 

 

HI

 

10.54

 

36.84

 

85.86

 

 

  GA and GAM (5%) = genetic advance at 5% selection intensity and genetic advance as percent of mean respectively. H2 = heritability in broad sense in percent.  DH=days to heading, DM= days to maturity, PH= plant height, SL= spike length, NSSP= number of spikelet’s per spike, NKSP=No of kernel per spike, BMS=biomass yield kg/ha, TKW= thousands kernel weight, YLD=yield kg/ha, HI= harvest index.

 

 

 


CONCLUSION

 

Based on this study genetic variability of bread wheat genotypes under high temperature stress condition evaluated for their traits revealed highly significant difference between the genotypes for most traits and significant difference among genotypes were observed. High genotypic coefficient of variation (GCV) and phenotypic coefficient of variation (PCV) values were observed for grain yield, biomass yield and harvest index. Moderate values for both GCV and PCV were obtained for traits indicated that traits were under control of additive genes and modified selection would be effective for improvement of the traits. Generally, the magnitude of difference between PCV and GCV values indicates the degree of influence of environment over genotypic effect. Heritability in broad sense accompanied with high genetic advance as percent of the mean was recorded for traits imply that phenotypic selection can be used to improve the traits. Overall from the study results it has been observed adequate existence of variability for most of the traits studied among genotypes. These genotypes could be exploited in wheat improvement and promising for development of heat stress tolerant varieties in future bread wheat breeding for high temperature stress condition.

 

 

REFERENCES

 

Ali, Y., Atta, B. M., Akhter, J., Monneveux, P., & Lateef, Z. (2008). Genetic variability, association and diversity studies in wheat (Triticum aestivum L.) germplasm. Pak. J. Bot, 40(5), 2087-2097.

Allard, R. W. (1960). Principles of Plant  Breeding John Wiley and Sons. Inc. New York.

Amsal. T. (2001).  Studies of Genotypic Variability and Inheritance of Waterlogging Tolerance in Wheat. Ph.D. Dissertation. University of the Free State, Bloemfontein, South Africa.

 Ashfaq, S., Ahmad, H. M., Awan, S. I., & Muhammad, S. A. K. (2014). Estimation of genetic variability, heritability and correlation for some morphological traits in spring wheat. Journal of Biology, Agriculture and Healthcare. 5(4), 10-16.

Awale, D., Takele, D., & Mohammed, S. ( 2013). Genetic variability and traits association in bread wheat (Triticum aestivum L.) genotypes. International Research Journal of Agricultural Sciences, 1(2):19-29.

Bhushan, B., Bharti, S., Ojha, A., Pandey, M., Gourav, S. S., Tyagi, B. S., & Singh, G.(2013). Genetic variability, correlation coefficient and path analysis of some quantitative traits in bread wheat. Journal of Wheat Research5(1), 21-26.

Bilgin, O., Korkut, K. Z., Baser, I., Daglioglu, O., Ozturk, I., Kahraman, T. & Balkan, A. (2011). Genetic variation and inter-relationship of some morpho-physiological traits in durum wheat (Triticum durum. L.) Desf.). Pak. J. Bot43(1), 253-260.

BurtonNW (1952). Quantitative inheritance in grasses. Proc.Intl …Natl. Academy of Science., 96, 5952-5959.

Burton, G. W., & Devane, E. H. (1953). Estimating heritability in tall fescue (Festuca Arundinacea) from replicated clonal material. Agronomy Journal45(10), 478-481.

CSA (Central Statistical Agency), 2018. Report on Area and Production of Major Crops (Private Peasant Holdings, Meher Season). Agricultural Sample Survey. Central Statistics Agency, Addis Ababa, Ethiopia.

Desta, G., Mihratu, A., Tolesa, D., Hailu, M., & Tadiyos,B. (2017). Enhancing Sustainable Wheat Productivity and Production through Development of Wheat Varieties Best Adapted to Irrigate Lowland Areas of Ethiopia, International Journal of Agriculture Innovations and Research, 2(6) 2319-1473.

Gomez, K. A., Gomez, K. A., & Gomez, A. A. (1984). Statistical procedures for agricultural research. John Wiley & Sons.

Haq, M.M.G., Hassan, Fakharuddin, Khalil, Z., Iqbal, N., Ullah,U., Ataullah.(2016).  Estimation of heritability and genetic advance in F3 populations of wheat. Pure and Applied Biology 5(4), 773-781. 

Johnson, H.W., Robinson, H.F. and Comstock, R.E. (1955a). Estimates of genetic and environmental variability in soybeans. Agronomy Journal. 47: 314-318.

Johnson, H. W., Robinson, H.F., & Cosmtock, R. G. (1955b). Genotypic and phenotypic correlation in soybean and their implication in selection. Agronomy Journal, 47: 477483.

Kaddem, W.K., Marker, S., Lavanya, G.R. (2014). Investigation of genetic variability and correlation analysis of wheat (Triticum aestivum L.) genotypes for grain yield and its Component traits european academic research. 2(5), 6529-6538.

Kalimullah, S., Khan, J., Irfaq, M., & Rahman, H. U. (2012). Gentetic variability, correlation and diversity studies in bread wheat (Triticum aestivum L.) germplasm. Journal of Animal & Plant Sciences22(2), 330-333.

 Kahrizi, D., Cheghamirza, K., Kakaei, M., Mohammadi, R., & Ebadi, A. (2010). Heritability and genetic gain of some morphophysiological variables of durum wheat (Triticum turgidum var. durum). African Journal of Biotechnology9(30), 4687-4691.

Kumar, B., Singh, C.M., & Jaiswal, K.K. (2013). Genetic Variability, Association and Diversity Studies in Bread Wheat (Triticum aestivum L.). An International Quarterly Journal of Life Sciences, 8(1): 143-147.

Larik, R.S & Joshi, A.B. (2004). Correlation, path coefficients and the implication of discriminate function for selection in wheat. Journal of plant Breeding 25, 383-392.

Mason, N. M., Jayne, T. S., & Shiferaw, B. A. (2012). Wheat Consumption in Sub-Saharan Africa: Trends, Drivers, and Policy Implications. East Lansing, MI: Michigan State University, Department of Agricultural, Food, and Resource Economics.

Mohammad, R., & Amri, A. (2011). Graphic Analysis of Trait Relations and Genotype Evaluation in Durum Wheat. Journal of Crop Improvement, 25(6), 680- 96.

Mihratu, A., Desta, G., Hailu M.,Tadiyos, B. (2019). Evaluation and Development of Bread wheat Varieties adapted to irrigated lowland areas of Ethiopia. Acad. Res. J. Agri. Sci. Res. 7(1): 37-41

Navin, K., Markar, S., Vijay, K. (2014). Studies on heritability and genetic advance estimates in timely sown bread wheat (Triticum aestivum L.). Bioscience Discovery. 5(1), 64-69. 

Oniya, V. N., Okechukwu, E. C., Atuhwu, A. I., & Akpan, N. M. (2017). Genetic Variability Studies on Twelve Genotypes of Rice (Oryza sativa L.) for Growth and Yield Performance in South Eastern Nigeria. Notulae Scientia Biologicae, 9(1), 110. https://doi.org/10.15835/nsb919980

Pramoda, H.P. & Gangaprasad, S. (2007). Biometrical basis of handling segregation population for improving productivity in onion (Allium cepa L.).  Journal of Asian Horticulture 3: 278-280

Pratap, N., Singh, P. K., Shekhar, R., Soni, S. K., & Mall, A. K. (2012). Genetic Variability, Charater Association and Diversity Analyses for Economic Traits in Rice (Oryza sativa L .). SAARC J.Agri., 10(2), 83–94.

Sivasubramanian, S., & MadhavaMenon, P. (1973). Genotypic and phenotypic variability in rice, Madras Agricultural Journal, 60, 1093-1096.

Sumanth, V., Bg, S., Ram, B. J., & Srujana, G. (2017). Estimation of genetic variability , heritability and genetic advance for grain yield components in rice ( Oryza sativa L .). Journal of Pharmacology and Phytochemistry, 6(4), 1437–1439.

Tabbal, J. A., Fraihat, A. H. A. (2012). Heritability Studies of Yield and Yield Associated Traits in Wheat Genotypes. Journal of Agricultural Sciences, 4(4), 11-22.

USDA (United States Department of Agriculture), 2017. Wlorld Agricultural Production accessed on April, 2017. Foreign Agricultural Service. 

Wendmagegn Chekol and Abere Mnalku.(2012).Selected physical and chemical characteristics of Soil of the middle Awash Irrigated Farm lands, Ethiopia.

 


 

Cite this Article: Tadiyos BS; Mihratu AK (2020). Genetic variability of yield and yield related traits in bread wheat (Triticum aestivum. L) Genotypes under high temperature condition. Greener Journal of Plant Breeding and Crop Science, 8(1): 06-12.