Genetic Variability Studies for Yield and Yield Related Traits in Elite Finger Millet [Elucine coracana (L.) Gaerten] Germplasm

Genetic Variability Studies for Yield and Yield Related Traits in Elite Finger Millet [Elucine coracana (L.) Gaerten] Germplasm

Aradhna Suman1 , Supriya Supal Surin2 , Sunil Kumar3 , Ekhlaque Ahmad4*

1Tilka Manjhi Agriculture College, Godda, Jharkhand , India

2Department of Genetics and Plant Breeding, Birsa Agricultural University, Ranchi, India

3Veer Kunwar Singh College of Agriculture, Dumraon, Bihar, India

4Zonal Research Station, Birsa Agricultural University, Chianki, Palamu Jharkhand-822102,

Corresponding Author Email: ekhlaque.bau@gmail.com

DOI : http://dx.doi.org/10.53709/CHE.2021.v02i04.010

Abstract

present study aims to study the existence of genetic variability and importance of some quantitative traits in the finger millet genotypes. The objectives were to assess the variability, heritability, and genetic advance for yield and thirteen yield component characters in the 55 elite finger millet genotypes. Highly significant mean sum of squares due to genotypes and wide range of variability were observed among the genotypes for all the characters studied. High genotypic coefficient of variation (GCV) was recorded for grain yield per plot (42.53), harvest index (31.12), grain yield per plant (29.42), biomass yield per plant (22.78), ears per plant (21.17) and effective tillers per plant (20.64) and high phenotypic coefficient of variation (PCV) was similarly recorded for grain yield per plot (42.55), harvest index (36.46), grain yield per plant (31.45), biomass yield per plant (23.85), ears per plant (22.98) and effective tillers per plant (23.08). High heritability coupled with high expected genetic advance as percent of mean was obtained for grain yield per plot (99.94, 87.60%), 1000 seed weight (99.87,36.72%), grain yield per plant (87.54, 56.71%), harvest index (86.50,59.62%),days to maturity (99.64,26.25%), days to 50% flowering (99.35, 35.89%), plant height (99.00,23.30%) ears per plant (84.84,40.17%) and leaf blast (94.88, 35.72%) indicating that the presence of more additive gene effects have ability for crop improvement and so these characters could be improved through selection. This study divulges that greater yield response could be obtained through direct selection scheme in finger millet genotypes.

Keywords

Finger millet, genetic variation, heritability and genetic advance

Download this article as:

1. INRODUCTION

Finger millet is one of the most important small millets crop grown in large areas of the developing world especially in Africa and Asia. It has the ability to produce higher yield than other crops under multiple stresses such as drought, soil acidity and land marginality. Moreover, it has high nutritional value and excellent storage qualities. In India it is extensively cultivated in Karnataka, Tamil Nadu, Orissa, Andhra Pradesh, Madhya Pradesh, Jharkhand and Bihar. In Jharkhand average production is very low. The low production of this region is primarily due to lack of high yielding varieties and poor management. There is need to increase the yield by the introduction of new high yielding germplasm lines.

Creation of genetic variability and selection for important traits is a decisive exercise that any plant breeder should apply to accomplish better yield and other desirable agronomic traits. However, to carry out potent selection, the information on available genetic variation among finger millet genotypes, the nature of component traits on which selection would be effective and the influence of environmental factors on each trait need to be known [1]. Information on the nature and magnitude of variability and heritability in a population is one of the prerequisites for successful breeding program in selecting genotypes with desirable characters [2]. It is therefore, of great consequence for breeders to know the heritability of the agronomical characters to improve the yield of the crop effectively.  According to Falconer and Mackay [3], heritability is defined as the measure of the correspondence between breeding values and phenotypic values. Thus, heritability plays a predictive role in breeding, expressing the reliability of phenotype as a guide to its breeding value. It is the breeding value which determines how much of the phenotype would be passed onto the next generation [4]. There is a direct relationship between heritability and response to selection, which is referred to as genetic advance. High genetic advance with high heritability estimates offer the most effective condition for selection [5]. The utility of heritability therefore increases when it is used to calculate genetic advance, which indicates the degree of gain in a character obtained under a particular selection pressure. Thus, genetic advance is yet another important selection parameter that aids breeder in a selection program. Hence, this study was done with the objective to assess the variability, heritability and genetic advance of grain yield and some of its related components to select a more desired trait that may contribute for the improvement of finger millet.

2. MATERIALS AND METHODS

2.1 Experimental site and design

A set of 50 germplasm with four checks and one filler germplasm of finger millet obtained from coordinating unit millet, Bangluru were evaluated in augmented randomized block design at small millets experimental area of Ranchi Agricultural College, Birsa Agricultural University, Kanke, Ranchi during Kharif 2015. List of germplasm along with checks is presented Table 1. Each germplasm was represented by a single row plot of 3 m length with inter and intra-row spacing of 22.5 cm and 10 cm, respectively. Recommended agronomic practices were followed to raise a good crop. Data were recorded on five randomly selected competitive plants at different growth stages of the crop for the 16 characters viz., days to 50%  flowering, flag leaf area (sq. cm ), Plant height (cm), number of effective tillers per plant, number of ears per plant, number of fingers per ear, finger length (cm), days to maturity,  grain yield per plant (g), grain yield per plot (g), biomass yield per plant (g), harvest index (%), 1000 – seed weight (g), disease reaction (0-5 scale), lodging susceptibility. Their adjusted mean value was subjected to statistical analysis using INDOSTAT software packages.

2.3 Statistical data analysis 

2.3.1 Estimation of magnitude of variation  

The mean value of the recorded data was subjected to analysis of variance (ANOVA) using the statistical analysis procedures of Sharma (1998) [6]. The phenotypic and genotypic variances were also estimated according to the method suggested by Burton and De Vane (1953) [7] using the formula:  

σ2g      =

σ2p = σ2g+σ2e

σ2e = MSe

Where, σ2g = genotypic variance, σ2p = phenotypic variance, σ2e = environmental variance, MST =        mean sum of square due to treatment, MSE = mean sum of square due to error, r = number of replication.

The coefficient of variations at phenotypic and genotypic level variation was estimated using the formula adopted by Johnson et al. (1955) [8] as: 

PCV = [σ2p ⁄ x‾] ×100

GCV = [σ2g ⁄ x‾] × 100

ECV = [σ2e ⁄ x‾] × 100

Where, σ2p = phenotypic standard deviation (σ2g + σ2e), σ2g = genotypic standard deviation and x‾ =grand mean for the characteristic, PCV, GCV and ECV = phenotypic, genotypic and environmental coefficient of variation respectively.

Table 1. List of experimental materials and their source

2.3.2 Estimate of heritability and expected genetic advance

Heritability (h2) in broad sense for all characters was computed using the formula adopted by Allard (1960) [9].

h2= [σ2g ⁄ σ2p] ×100

σ2p = σ2g + σ2e

Where, σ 2 g = genotypic variance, σ 2 p = Phenotypic variance, σ2e = error variance. Genetic advance as part of the mean (GA) for each character was computed using the formula by Allard (1960) [9].

GA = (K) (σp) (h2) and GMA (as percent of the mean) = [(GA)] ⁄ x‾ × 100

Where, k = selection differential (at 5% selection intensity), σp = phenotypic standard deviation, h2 = heritability and x‾ = grand mean.

Table 3. Genetic estimates for different yield and yield attributing characters and disease reaction

CharacterPCVGCVh2 %G.AGA Mean%
Days to 50% flowering17.5417.4899.3526.4235.89
Flag leaf area (cm2)16.4516.1996.9613.8832.85
Plant height (cm)11.4311.3799.0020.1423.30
Effective tillers per plant23.0820.6479.960.4938.02
Ears per plant22.9821.1784.840.5140.17
Fingers per ear16.6015.7990.442.3430.93
Finger length (cm)13.7812.7685.722.0724.34
Days to maturity12.7912.7799.6427.5126.25
Grain yield per plant(g)31.4529.4287.542.3156.71
Grain yield per plot(g)42.5542.5399.94118.8787.60
Biomass yield per  plant(g)23.8522.7891.2610.1344.84
Harvest index (%)33.4631.1286.5011.3259.62
1000-seed weight(g)17.8517.8399.870.8136.72
Leaf blast17.9717.5094.881.5735.13
Neck blast29.109.8811.523.256.91
Finger Blast28.4910.9314.714.1310.63

2.3.3 Harvest index: To find out harvest index each tagged plant is harvested separately at maturity just near to the soil surface and sun dried about 15 days. The harvested plant was threshed to find out the weight of grain and then the harvest index is calculated by a formula i.e.:

Harvest index = Economical weight ⁄Biological weight ×100

Table 4. Phenotypic variability for yield and yield contributing characters and disease reaction

CharactersRangeMean ±SEMσ2gσ2pσ2e
Days to 50% flowering50.75-117.7573.18±1.85165.60166.681.08
Flag leaf area (cm2)27.70-55.6942.24±1.0046.8648.331.47
Plant height (cm)64.62-107.6186.12±1.3996.6297.600.97
Effective tillers per plant1.00-2.601.30±0.040.070.080.01
Ears per plant0.96-2.251.29±0.040.070.080.01
Fingers per ear5.60-12.007.57±0.171.434.570.15
Finger length (cm)6..51-11.428.49±0.151.181.370.19
Days to maturity80.41-147.41104.95±1.90178.98179.620.64
Grain yield per plant (g)1.79-10.184.18±0.191.441.640.20
Grain yield per plot (g)34.69-392.35139.33±8.513332.093334.192.10
Biomass yield/plant (g)12.00-38.7322.73±0.7826.5129.052.54
Harvest index (%)8.14-45.2419.30±0.9534.9440.405.45
1000-seed weight (g)1.38-3.332.23±0.050.150.150.00
Leaf blast2.00-5.004.52±0.110.610.650.03
Neck blast (ASIN)6.65-67.2546.04±1.8721.65187.91166.25
Finger Blast (ASIN7.22-16.7446.77±1.8727.34185.85158.50

3. RESULT AND DISSCUSION

The result of ANOVA of thirteen yield related traits for the fifty five genotypes is presented in Table 2. The ANOVA showed significant differences among the tested genotypes for all the characters except for the neck blast and finger blast indicating the presence of variability which can be utilized through selection.

The estimate of both phenotypic (PCV) and genotypic coefficients of variation (GCV) for all the characters are presented in Table 3. The variability estimates revealed close relation between PCV and GCV. In general, variability estimates showed that the estimate of PCV were greater than those of GCV for all the traits, this suggested the role of environment in the expression of the characters. Highest GCV was obtained for grain yield per plot (42.53) followed by harvest index (31.12), grain yield per plant (29.42), biomass yield per plant (22.78), ears per plant (21.17) and effective tillers per plant (20.64). The higher estimate of PCV (42.55) in comparison to GCV (42.53) for grain yield per plot suggested environmental influence on this character. The least difference between PCV and GCV (Table 4) for plant height 1000 seed weight suggested that this character is less affected by environment. In such condition, selection can be effective on the basis of phenotype alone with equal probability of success. These results match with the findings of [10] [11] and [12] for single plant grain yield, thousand grain weight, flag leaf blade length, finger number per panicle and 1000 seed weight.

Table 2. Analysis of variance (mean sum squares) for thirteen yield attributing characters and disease reaction

*, ** & *** = significant at p = 0.05, 0.01 & 0.001 respectively

COMPETING INTERESTS

Authors    have    declared    that    no    competing interests exist.

On the basis of GCV, it is possible to determine the amount of heritable variation. It can be found that with greater degree of accuracy when heritability in conjunction with genetic advance is studied [8]. Hence, both heritability and genetic advance were determined to study the scope of improvement in various characters through selection. The heritability estimate ranged from 11.52% for neck blast to 99.94% for grain yield per plot. Among all the characters, high magnitude of heritability was recorded for grain yield per plot (99.94%), followed by 1000-seed weight (99.87%), days to maturity (99.64 %), days to 50% flowering (99.35%), plant height (99.00), flag leaf area (96.96%), biomass yield per plant (91.26%), fingers per ear (90.44%), grain yield per plant (87.54%), ears per plant (84.84%) and effective tillers per plant (79.96%) indicated that environmental effects constitute a sufficient portion of total phenotypic variation and hence selection for those characters will be less effective. Similarly high heritability for all the characters studied was reported by [12], for plant height by [10], for days to 50 per cent flowering by [13] and for thousand grain weight by [14].Genetic mean as percent mean for various characters (Table 2) revealed that grain yield per plot, harvest index and grain yield per plant showed high genetic advance. These characters exhibited high GCV, heritability together with high genetic advance indicating the predominance of additive gene effects in controlling these characters. These results match with the findings of [15] for tillers per plant, length of finger and grain yield per plant and [16] for fertile tillers per plant, length of finger and grain yield per plant.

 4. Conclusion  The PCV and GCV values were high for grain yield per plot, harvest index, grain yield per plant, biomass yield per plant, ears per plant and effective tillers per plant suggesting the possibility of improving these traits through selection. The difference between PCV and GCV values was least for 1000 seed weight indicating less influence of the environment on the expression of these characters.  High heritability coupled with high expected genetic advance as percent of mean for grain yield per plot, harvest index and grain yield per plant. Therefore, these characters could be improved more easily than the other characters.  

REFERENCES

  1. Jaleta Z, Ayana A, Habitamu Zeleke. Variability, Heritability and Genetic Advance for some yield and yield related traits in Ethiopian Barley (Hordium vulgare L.) landraces and crosses. Int. J. Plant Breed. Genet. 2011 5 (1): 44-52.
  2. Dudly JW, Moll RH. Interpretation and use of estimates of heritability and genetic variance in plant breeding. Crop Sci. 1969 9: 257-267.
  3. Falconer DS, Mackay FC. Introduction to Quantitative Genetics. Longman, New York. 1996 p. 464.
  4. Larik AS, Malik SI, Kakar AA, Naz MA. Assesment of heritability and genetic advance for yield and yield components in Gossypium hirsutum L. Scientific Khyber. 2000 13: 39-44.
  5. Tazeen M, Nadia K, Farzana NN. Heritability, phenotypic correlation and path coefficient studies for some agronomic characters in synthetic elite lines of wheat. J. Food. Agric. Environ. 2009 7(3&4): 278 – 282.
  6. Sharma JR. Statistical and Biometrical Techniques in Plant Breeding. New Age International (P) Limited Publishers, New Delhi. 1998 p. 432.
  7. Burton GW, de vane EH. Estimating heritability in Tall Fescue (Festuca Arundinacea) from replicated clonal material. Agron. J. 1953 45: 481-487.
  8. Johnson HW, Robinson HF, Comstock RE. Estimates of genetic and environmental variability in soybeans. Agron. J. 1955 47: 314-318.
  9. Allard RW. Principles of Plant Breeding. John Willey and Sons, New York. 1960 p. 485.
  10. Dagnachew L, Kassahun T, Masresha F and Santie DV. Inheritance and Association of Quantitative Traits in Finger Millet (Eleusine coracana Subsp. Coracana) Landraces Collected from Eastern and South Eastern Africa. International Journal of Genetics. 2012 2(2): 12-21.
  11. Nirmalakumari A, Salini K and Veerabadhiran P. Morphological Characterization and Evaluation of Little millet (Panicum sumatrense Roth. ex. Roem. and Schultz.) Germplasm. Electronic Journal of Plant Breeding, 2010 1(2): 148-155.
  12. Kebere B, Prapa S, Wasana W and Vipa H. Genetic Variation, Heritability and Path-Analysis in Ethiopian Finger Millet [Eleusine coracana (L.) Gaertn] Landraces. Kasetsart J. (Nat. Sci.) 2006  40: 322 – 334.
  13. Dhagate NK, Patidar GL, Shrivastava PS and Joshi RC.  Correlation and genetic variability study in ragi [Eleusine coracana (L.) Gaertn]. JNKVV Research J. 1972 6:121-124.
  14. Udamala, A, Vijayalakshmi B, Anuradha, N, Patro, TSSK. and Sekhar V.  Studies on Genetic Variability for Yield and Quality Traits in Finger Millet (Eluesine coracana L. Gaertn). Int. J. Current Microbiology and Applied Sciences, 2020 9(9): 641-649.
  15. Priyadharshani C, Nirmal k, John AJ and Raveendran A. Genetic variability and trait relationships in finger millet (Eleusine coracana L) Hybrids. Madras Agricultural Journal. 2011 98:18-21.