Genetic Diversity and Yield Determinants in Maize (Zea Mays L.)

DOI : 10.17577/IJERTCONV13IS06041

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Genetic Diversity and Yield Determinants in Maize (Zea Mays L.)

Liban Said Ali1, P.N. Verma2, Usman Sayeed3

1M.Sc. (Agriculture), Department of Agriculture, Integral Institute of Agricultural Science & Technology, Integral University, Lucknow-226026 (INDIA)

2,3Assistant Professor Department of Agriculture, Integral Institute of Agricultural Science & Technology, Integral University, Lucknow-226026 (INDIA)

**Corresponding author: pnverma@iul.ac.in

Abstract

Genetic analysis of variability, heritability and character association was studies among 18 maize F1 hybrids for eleven traits. The analysis of variance revealed that genotypic mean squares were significant for all traits, indicating that all the F1 hybrids under study had a higher level of genetic diversity. In terms of genotypic and phenotypic coefficient variation, the most significant coefficient was found in plant height (10.129 and 11.907), 100 seeds weight (9.393 and

14.008), seed yield per cob (9.366 and 11.931), grain yield per plant (8.654 and 12.054), respectively. The Grain yield per plant has shown highly significant positive correlations with seed yield per cob (0.908), 100-seed weight (0.879), number of grains per row (0.722), cob length (0.701), cob diameter (0.715), number of rows per cob (0.526), plant height (0.431), and indicate a close genetic association between traits favouring larger seed size and increased seed yield per cob with augmented grain yield per plant might all be employed as selection criteria to increase the maize grain yield.

Keywords: Genetic variability, diversity, heritability, genetic advance.

Introduction

Maize, scientifically known as Zea mays L., is a cereal crop from the Poaceae (Gramineae) family and Maydeae tribe, boasting a diploid chromosome number of 2n=2x=20. Renowned for its adaptability and resilience to varying Agro-climatic conditions, maize holds a pivotal

commercial position among grain crops. Often hailed as the Queen of cereals within the Gramineae family, maize stands out due to its exceptional productivity potential.The crop has gained global prominence, extending its cultivation from the equatorial regions to temperate zones, thriving in diverse environments.Global maize production, exceeding 1147.7 million metric tons annually, involves over

170 countries, with an average productivity of 5.75 tons per hectare. The United States, China, Brazil, and Argentina are significant producers, collectively contributing to over two-thirds of the world's production. In Asia, India and Indonesia play substantial roles.Maize grains are valued for their versatile applications, serving as a staple food, animal feed, and an essential raw material for various industrial products. The demand for maize in developing countries is estimated to double by the year 2050 (Rosegrant et al. 2009).

Key maize-growing states in India include Andhra Pradesh, Karnataka, Rajasthan, Maharashtra, Bihar, Uttar Pradesh, Madhya Pradesh, and Himachal Pradesh. Uttar Pradesh, particularly the upper Gangetic Plain, emerges as a prominent maize producer, with significant production centres in Bulandshahar, Jaunpur, and Ghaziabad districts. Maize

cultivation in India predominantly occurs as a rain-fed Kharif crop, sown before the monsoon and harvested afterwards. Uttar Pradesh, however, also cultivates maize during the Rabi season before the onset of winter.The main objective of maize breeding programs worldwide is to improve grain yield and it is a continuous process of creating variability, selecting superior lines from a pool, and utilizing them to achieve this goal. An assessment of variability and heritability is necessary to make an effective artificial selection and to understand variation in the material (Begum et al. 2016). Effective breeding programs rely on assessing genetic diversity and variability within maize populations, ensuring the development of superior cultivars. Parameters like phenotypic and genotypic coefficients of variation aid in evaluating the extent of variation within maize varieties, laying the foundation for successful varietal/hybrid development initiatives. The selection process is most effective when there is ample variability in the base material. Hence, it is more important to assess variability in the base material for artificial selection before exercising selection. It is possible to assess variability by using genetic parameters such as range, phenotypic coefficient of variation (PCV) and genotypic coefficient of variation (GCV) (Sesay et al. 2016). Despite the

presence of variability, the efficiency of selection is influenced by heritability and selection intensity (Dudly and Moll 1969). The estimates of broad sense heritability and genetic advance as a percent of mean (GAM) provides a reliable information about the heritable portion of the trait. High broad sense heritability along with high GAM also indicates the presence of additive gene action and hence selection could be effective (Nwangburuka et al. 2012).Besides variability it is also necessary to know the association of various characters to the trait of economic interest i.e., grain yield. Since, grain yield is a complex trait it is affected by several yield-related characters, selection based on yield attributes is more effective (Grafius 1956). So, a detailed description of the associations between grain yield and other yield contributing characters is more valuable, which can be obtained by a correlation study. Additionally, dividing the correlation into direct and indirect effects by path analysis allows a better understanding of the influence of each yield attributing trait on yield, which in turn helps to design the selection strategy (Azam et al. 2014). Hence, the present study was undertaken to assess variability and association of various quantitative traits in maize using twenty-five maize inbred lines as a base material.

Materials and Methods

The present research was carried out during kharif season 2023at Instructional Farm Unit-4, Integral Institute of Agricultural Science and Technology, Integral University, Lucknow (UP), India. The experimental material comprised 18 diverse maize F1hybrids sourced from various regions of Uttar Pradesh, India. The experiment was conducted in a randomized complete block design with three replications. Each plot consisted of a single row of plants sown using the line sowing method at a depth of 3-5 cm, with a row-to-row spacing of 60 cm and a plant-to-plant spacing of 30 cm. A total of 54 plots were utilized for the study.Five randomly selected plants from each of the was selected for recording the observations on various traits.

Results and Discussion

In agricultural research, ANOVA serves as a fundamental statistical tool for understanding the variability within and between different components of a study. The ANOVA results indicate significant variations among genotypes for most of the studied traits. This suggests that genetic factors play a crucial role in determining the performance of maize hybrids across different traits. Further

analysis can help in identifying superior genotypes for enhanced agricultural productivity and quality (table-1).

The current study revealed distinct levels of genotypic coefficient of variance (GCV) across various traits. Traits exhibiting high GCV include plant height (10.129%), 100 seeds weight (9.393%), seed yield per cob (9.366%), grain yield per plant (8.654%), plant height (10.129%) and cob diameter (5.618%). These traits showcase significant genetic variation within the population, indicating the potential or diverse phenotypic expressions among individuals. Moderate GCV were observed in traits such as cob length (4.182%), days to 50% tasseling (3.875%), number of grains per row (3.305%), days to 50% silking (2.902%), and number of rows per cob (2.808% While these traits display variability, they are of a moderate degree compared to those with high GCV. Conversely, days to maturity (1.84) emerge as a trait with low genotypic coefficient of variance (GCV), suggesting minimal genetic variation in the population regarding the time required for maturity (table-3). Earlier high GCV and PCV for grain yield and moderate GCV and PCV for cob characters were observed by Jilo et al. (2018) and Magar et al. (2021), where they suggested moderate to high GCV and PCV provides opportunity

to practice selection in the genotypes for the trait improvement.The present study offers insight into the phenotypic coefficient of variance (PCV) across various traits, akin to the earlier analysis based on the genotypic coefficient of variance (GCV). Traits demonstrating high PCV include grain yield per plant (12.054%), plant height (11.907%), 100 seeds weight (14.008%), and seed yield per cob (11.931%). These traits exhibit substantial phenotypic variation within the population, indicating diverse phenotypic expressions among individuals. Traits with moderate PCV encompass cob diameter (8.351%), number of rows per cob (5.152%), days to 50% tasseling (4.116%), cob length (5.611%), and number of grains per row (4.966), days to 50% silking (3.183) (table-3).Genotypic and phenotypic variances were determined according to Singh and Chaudhary (1985) using MS-Excel programme.

Traits exhibiting high heritability, including days to 50% tasseling (88.638%), days to 50% silking

(83.117%), plant height (72.37%), days to maturity (66.246%), seed yield per cob (61.624%), cob length (55.54%) and grain yield per plant (51.549%) suggest that a significant portion of their phenotypic variance stems from genetic differences among individuals rather than

environmental influences.Thus, these traits hold promise for substantial enhancement through selective breeding endeavours. the genetic advance percentage estimates the anticipated improvement in a trait through selection. Traits with higher genetic advance percentage mean, such as plant height (17.751%), seed yield per cob (15.145%), and grain yield per plant (12.8%), signify more significant potential for enhancement through selective breeding. Conversely, traits with lower genetic advance percentage mean, like days to 50% tasselling (7.516%), days to 50% silking (5.451%), and a number of rows per cob (3.153%), may necessitate more nuanced breeding approaches or may exhibit inherent limitations in their improvement potential (table-3).Even though the trait has high variability in terms of GCV and PCV, the effectiveness of the selection could be evaluated only based on the heritable portion of the character. Which could be identified based on heritability and genetic advances as a percent of mean (Rao and Rao 2015). In general, high broad-sense heritability coupled with high GAM for the trait, is considered to have a positive response to the phenotypic selection (Wali et al. 2019). Wedwessen and Zeleke (2020) also observed high heritability with high GAM for grain yield, hundred grain weight, number of kernels per row and cob length

supporting the findings of the present study. Thus, it is recommended to consider heritability and GAM together to predict the response of selection (Ogunniyan and Olakojo 2014).

Table-1. Analysis of Variance (ANOVA)

Df

DT

DS

CL

CD

NR/C

NG/R

DM

PH

HSW

SY/C

GY/P

Replication

2

0.2468

0.2198

0.3332

0.1539

0.0305

2.6352

3.7055

470.55

12.5895

58.109

200.522

Genotypes

17

16.3924**

10.7815**

1.6924**

1.6834**

0.5579**

2.9339**

8.9865**

1314.56**

17.3834**

140.241**

302.491**

Errors

34

0.6717

0.6837

0.3564

0.4835

0.246

0.8667

1.3047

148.41

5.0365

24.107

72.158

** = Significant at 1 % and * = Significant at 5 % level of significance

Table-2. Treatment Means and Overall Means

Genotypes

GY/P

DT

DS

CL

CD

NRC

NGR

DM

PH

HSW

SY/C

UM-10

98.377

56.700

61.200

15.733

10.587

11.740

23.000

87.190

207.067

20.427

65.583

UM-20

90.035

59.987

63.717

15.373

10.663

11.923

25.650

87.507

174.187

19.823

60.673

UM-30

98.295

60.683

64.413

16.503

11.793

11.370

26.550

87.087

224.527

22.270

66.180

UM-40

114.150

59.280

63.010

15.390

10.680

11.620

26.607

88.820

169.833

25.423

76.750

UM-50

109.670

59.020

62.750

16.937

12.227

11.840

26.140

88.383

203.163

24.317

73.763

UM-60

113.805

60.493

64.223

16.380

11.670

11.810

26.600

88.660

218.457

23.820

76.520

UM-70

108.960

59.090

62.820

17.173

12.463

11.710

25.277

86.030

200.583

22.707

70.923

RASI-4212

104.480

61.817

65.547

15.797

11.087

11.733

24.810

85.593

176.283

18.867

59.870

MANGALAM

108.615

62.420

66.150

16.143

11.433

11.633

25.270

85.870

201.887

23.480

61.903

KAVERI-2021

103.565

63.687

67.417

17.173

12.463

11.567

24.330

89.980

212.500

23.947

67.410

TRIMURTI-826

81.797

56.533

61.100

14.620

11.323

10.663

23.650

85.363

168.457

17.960

54.530

VIRAT

84.850

56.500

61.933

16.167

9.563

11.293

24.320

84.717

167.847

16.653

56.563

VARDAN-1108

93.107

56.600

61.533

15.610

11.320

10.740

25.220

84.297

218.187

19.100

62.070

KANCHAN-101

108.963

56.567

61.200

16.403

11.030

10.990

25.277

86.030

163.493

22.253

72.640

SRI-5455

104.483

56.567

61.100

15.027

11.080

11.210

24.810

85.593

196.823

21.147

69.653

PIO-3401

108.617

56.567

61.533

15.373

11.220

11.180

25.270

85.870

212.117

21.827

72.410

PBM-101

103.565

60.770

64.500

16.403

11.693

12.370

24.330

89.980

213.407

23.597

69.693

DHM117

86.985

59.990

63.720

15.027

10.317

11.293

24.980

88.153

174.797

21.130

58.640

Overall Mean

101.240

59.071

63.215

15.957

11.256

11.483

25.116

86.951

194.645

21.597

66.432

Table-3. Heritability, Genotypic Coefficient of Variation % & Phenotypic Coefficient of Variation % (GCV & PCV)

Response Variable

Range

Grand mean

SEm

SED

Heritability

GCV

PCV

Gen- Advance

Gen-Adv

% Means

GY/P

127.80-76.41

101.23

4.9043

14.095

51.549

8.654

12.054

12.959

12.8

DT

64.78-56.40

59.07

0.4732

1.36

88.638

3.875

4.116

4.44

7.516

DS

68.51-61.00

63.21

0.4774

1.372

83.117

2.902

3.183

3.446

5.451

CL

17.42-14.17

15.95

0.3447

0.991

55.54

4.182

5.611

1.024

6.42

CD

12.71-9.12

11.25

0.4015

1.154

45.268

5.618

8.351

0.877

7.787

NR/C

12.95-10.34

11.48

0.2864

0.823

29.71

2.808

5.152

0.362

3.153

NG/R

27.56-21.32

25.11

0.5375

1.545

44.29

3.305

4.966

1.138

4.531

DM

91.13-83.23

86.95

0.6595

1.895

66.246

1.84

2.261

2.683

3.086

PH

232.64-153.12

194.64

7.0335

20.214

72.37

10.129

11.907

34.551

17.751

HSW

28.29-16.21

21.59

1.2957

3.724

44.969

9.393

14.008

2.802

12.976

SY/C

85.85-50.94

66.43

2.8347

8.147

61.624

9.366

11.931

10.061

15.145

Days to 50% Tasseling (DT), Days to 50 % silking (DS), Plant height (PH), Days to maturity (DM), Cob length (CL), Cob diameter (CD)

No. of Grain rows per cob (NG/R), No. of Grains per row (NR/C), Hundred grain weight (HSW), Seed yield per cob (SY/C), Grain yield per plant (GY/P)

Table-4. Correlation Matrix (Above diagonal Genotypic and below diagonal Phenotypic)

GY/P

DT

DS

CL

CD

NRC

NGR

DM

PH

HSW

SY/C

GY/P

1.000

0.35NS

0.305NS

0.701**

0.715**

0.526*

0.722**

0.375NS

0.431*

0.879**

0.908**

DT

0.840 **

1.000

0.986**

0.497*

0.507*

0.790**

0.297NS

0.655**

0.266NS

0.620**

0.051NS

DS

0.197 NS

0.983 **

1.000

0.500*

0.444*

0.715**

0.213NS

0.590**

0.275NS

0.543**

-0.021NS

CL

0.142 NS

0.390 **

0.398 **

1.000

0.671**

0.607**

0.210NS

0.437*

0.470*

0.731**

0.541**

CD

0.230 NS

0.365 **

0.331 *

0.569 **

1.000

0.416*

0.213NS

0.429*

0.753**

0.800**

0.546**

NR/C

0.286 NS

0.426 **

0.377 **

0.338 *

0.082 NS

1.000

0.297NS

0.878**

0.338NS

0.868**

0.434*

NG/R

0.329 *

0.224 NS

0.181 NS

0.241 NS

0.260 NS

0.038 NS

1.000

0.199NS

0.145NS

0.901**

0.724**

DM

0.285 NS

0.492 **

0.422 **

0.235 NS

0.234 NS

0.505 **

0.207 NS

1.000

0.235NS

0.983**

0.524**

PH

0.278 NS

0.214 NS

0.216 NS

0.365 **

0.461 **

0.156 NS

0.162 NS

0.242 NS

1.000

0.582**

0.435**

HSW

0.232 NS

0.314 *

0.230 NS

0.226 NS

0.378 **

0.201 NS

0.202 NS

0.415 **

0.175 NS

1.000

0.853**

SY/C

0.727 **

0.016 NS

-0.048 NS

0.267 NS

0.329 *

0.263 NS

0.346 *

0.379 **

0.270 *

0.770 **

1.000

** = Significant at 1 % and * = Significant at 5 % level of significance

Table-5. Estimate of direct (diagonal) and indirect effects (off diagonal) at genotypic level

DT

DS

CL

CD

NR/C

NG/R

DM

PH

HSW

SY/C

DT

0.228

0.051

-0.039

-0.012

0.056

-0.004

-0.128

0.004

0.027

0.015

DS

0.224

0.051

-0.040

-0.011

0.050

-0.003

-0.110

0.004

0.020

-0.042

CL

0.089

0.020

-0.101

-0.018

0.045

-0.004

-0.061

0.006

0.019

0.235

CD

0.083

0.017

-0.057

-0.032

0.011

-0.004

-0.061

0.008

0.032

0.289

NR/C

0.097

0.019

-0.034

-0.003

0.131

-0.001

-0.131

0.003

0.017

0.231

NG/R

0.051

0.009

-0.024

-0.008

0.005

-0.017

-0.054

0.003

0.017

0.303

DM

0.112

0.022

-0.024

-0.007

0.066

-0.004

-0.260

0.004

0.035

0.333

PH

0.049

0.011

-0.037

-0.015

0.021

-0.003

-0.063

0.018

0.015

0.237

HSW

0.072

0.012

-0.023

-0.012

0.026

-0.003

-0.108

0.003

0.085

0.675

SY/C

0.004

-0.002

-0.027

-0.010

0.035

-0.006

-0.099

0.005

0.065

0.877

Residual value: 0.211

The genetic correlation experiment revealed valuable insights into the genetic relationships between grain yield per plant and various phenotypic traits. Grain yield per plant has shown highly significant positive correlations with seed yield per cob (0.908**), 100-seed weight (0.879**), number of grains per row (0.722**), cob length (0.701**), cob diameter (0.715**), number of rows per cob (0.526*), plant height (0.431*), and indicate a close genetic association between traits favouring larger seed size and increased seed yield per cob with augmented grain yield per plant (table-4).Pavan et al. (2011) reported a similar kind of association in their study. Similar results were also noticed by Devasree et al. (2020).Although the correlation coefficient indicates the association between the traits, it does not indicate their direct and indirect effects. By partitioning the correlation coefficient using path analysis, it is possible to calculate the direct and indirect effects (Wali et al. 2012). The information about the direction and magnitude of association of various quantitative traits help in indirect selection for grain yield in the breeding programme, as the direct selection of a complex trait like grain yield is ineffective due to the influence of many genes and the environment (Grafius 1956). The direct and indirect effects of eleven

characters on grain yield per plant estimated by path coefficient analysis using simple correlations are given in Table-5. The highest positive direct effect on grain yield per plant was exerted by seed yield per cob (0.877), days to 50% tasseling (0.228), 100 seeds weight (0.085), number of rows per cob (0.131), days to 50% silking (0.051) and plant height (0.018). Similarly, direct positive effect of hundred grain weight, number of kernel rows per cob and cob girth on grain yield was reported by Patil et al. (2016).The characters that contributed a negative direct effect on grain yield per plant were days to maturity (-0.260), cob length (-0.101), cob diameter (-0.032), and number of grains per row (-0.017).The highest positive indirect effect on grain yield was exerted by 100 seed weight (0.675) via seed yields per cob, days to maturity (0.333) via seed yields per cob, number of grains per row (0.303) via seed yields per cob, cob diameter (0.289) via seed yields per cob, plant height (0.237) via seed yields per cob, cob length (0.235) via seed yields per cob, number of rows per cob (0.231) via seed yields per cob.

The analysis of various traits contributing to genetic divergence in maize reveals that the most significant contributors are days to 50% tasseling (47.71%), 100 seeds weight

(18.95%), and plant height (13.07%), indicating their crucial role in differentiating genotypes and adaptation to different environments.Grain yield per plant (3.92%), days to 50% silking (3.27%), number of grains per row (3.27%), days to maturity (7.19%), and seed yield per cob (2.61%) also contribute to divergence, though to a lesser extent, highlighting their influence on yield and crop performance. Notably, cob length, diameter, and number of rows per cob show no contribution (0%), suggesting uniformity among these traits across genotypes (table-6).Understanding these contributions helps select traits for breeding programs to enhance yield, adaptation, and overall genetic improvement in maize.Cluster-1, the largest group with ten genotypes, indicates a high degree of genetic similarity among its members, suggesting a significant portion of shared genetic makeup is likely due to common ancestry or similar selective pressures(Madhav et al., 2016). Cluster-2, comprising six genotypes, is closely related but distinct enough to form a separate group from Cluster-1, potentially indicating different evolutionary paths or adaptations. Clusters-3 and 4 each contain only a single

genotype, with genotype 18 and genotype

3 representing unique genetic makeups that do not align closely with other clusters (table-7). Regarding other traits, Cluster 3 showed the highest means for days to 50% tasseling, days to 50% silking, cob length, number of grains per row, days to maturity, and plant height. Cluster 1 had the highest means for cob diameter and 100-seed weight, as well as the number of rows per cob and seed yield per cob.The clustering patterns suggest diverse genetic backgrounds and trait associations among the genotypes. These insights can guide selection of parents and design of cross combinations to maximize variability and yield improvement in maize breeding programs (table-8).The average intra- and inter-cluster distances between different clusters are presented in table-9. The intra- cluster D2 values ranged from 37.7244 (Cluster I) to 0 (Clusters II, III, IV), indicating varying compactness within the clusters. Regarding inter-cluster distances, the average D2 values suggested varying dissimilarity among clusters. The most diverse pairs were III and IV (528.4817), followed by I and IV (316.9605), I and III (176.3658), II and III (373.1148), II and IV (84.8648), and I and II (37.7244).

Grain yield/plant

3.92 %

Days to 50% tasseling

47.71 %

Days to 50% silking

3.26 %

Cob length

0

Cob diameter

0

No. of rows/cobs

0

No. of grains/rows

3.26 %

Days to maturity

7.18 %

Plant height

13.07 %

100 seeds weight

18.95 %

Seed yield/cob

2.61 %

Table-6. Contribution of various traits to divergence

Table-7.Number of genotypes in different cluster

Clusters

No. of genotypes

Genotypes

CLUSTER= 1

10

9 10 12 13 11 14 8 16 15 17

CLUSTER= 2

6

4 7 6 1 2 5

CLUSTER= 3

1

18

CLUSTER= 4

1

3

Table-8. Cluster mean

CLUSTER

GY/P

DT

DS

CL

CD

NR/C

NG/R

DM

PH

HSW

SY/C

1

60.36

64.09

16.11

11.40

11.73

25.62

87.61

195.71

22.54

67.49

103.86

2

56.59

61.28

15.46

11.09

11.09

24.54

85.72

194.36

20.45

66.15

99.22

3

63.69

67.42

17.17

12.46

11.57

24.33

89.98

212.50

23.95

67.41

103.57

4

56.50

61.93

16.17

9.56

11.29

24.32

84.72

167.85

16.65

56.56

84.85

Table-9. Inter and intra cluster distance

Cluster

I

II

III

IV

I

37.7244

176.3658

79.9711

316.9605

II

35.3815

373.1148

84.8648

III

0

528.4817

IV

0

This study investigated the genetic variability within a set of F1 maize hybrids, revealing substantial diversity for key agronomic traits. The significant genotypic variation observed for all traits underscores the potential for selection and improvement within this material. High heritability estimates for days to 50% silking and tasseling suggest these traits are primarily under genetic control, making them amenable to selection. Furthermore, the strong positive correlations observed between grain yield per plant and yield components such as seed yield per cob, 100-seed weight, and cob characteristics highlight the importance of these traits in determining yield potential. Path coefficient analysis confirmed the direct and positive influence of these yield components on grain yield, indicating their utility as selection criteria in breeding programs.

Acknowledgement

The author acknowledge the support of Integral University, Lucknow for providing all the logistic support in conduct of the experiment and UPCAR for having used their genetic material.

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