INDIAN JOURNAL OF PURE & APPLIED BIOSCIENCES

ISSN (E) : 2582 – 2845

  • No. 772, Basant Vihar, Kota

    Rajasthan-324009 India

  • Call Us On

    +91 9784677044

Archives

Indian Journal of Pure & Applied Biosciences (IJPAB)
Year : 2020, Volume : 8, Issue : 4
First page : (204) Last page : (208)
Article doi: : http://dx.doi.org/10.18782/2582-2845.8239

Genetic Variability, Heritability and Genetic Advance for Growth, Yield and Quality of Fenugreek (Trigonella foenum-graecum L.)

Manider Jeet Singh1*, Rakesh Kumar Meena2, S. K. Trivedi3 and Lokesh Kumar4
1Corresponding author, 2Supervisor, 3Dean, 4M.Sc. Student
School of Agricultural Sciences, Department of Horticulture,
Career Point University, Kota (Rajasthan)
*Corresponding Author E-mail: maninderbrar80588@gmail.com
Received: 22.06.2020  |  Revised: 29.07.2020   |  Accepted: 3.08.2020 

 ABSTRACT

The mean performance of the genotypes revealed the variation was highest for seed yield per plot, days taken to maturity, germination percentage. The PCV was higher than the GCV for all the characters. High PCV and GCV were observed for weight of seeds per pod, seed yield (q/ha-1), length internodes, number of pods per plant. High heritability coupled with high genetic advance for traits such as a like seed yield, weight of pod, weight of seed per pod. All the characters except number of branches at 90 DAS, germination percentage and days taken to maturity were found to be significant, which indicates high extent of genetic variability for all the traits under study.

Keywords: genotypes, germination, Fenugreek, Heritability                                                                                                                                                                                                                                                                                           

Full Text : PDF; Journal doi : http://dx.doi.org/10.18782

Cite this article: Singh, M.J., Meena, R.K., Trivedi, S.K., & Kumar, L. (2020). Genetic Variability, Heritability and Genetic Advance for Growth, Yield and Quality of Fenugreek (Trigonella foenum-graecum L.), Ind. J. Pure App. Biosci. 8(4), 204-208. doi: http://dx.doi.org/10.18782/2582-2845.8239

INTRODUCTION

The fenugreek (Trigonella foenum-graecum L.) belongs to the family Fabaceae and is a multiuse and commercially important spice crop grown for its seeds, tender shoots, and fresh leaves. It is a small-seeded self pollinated, diploid annual legume plant with 2n= 16, grown as spice-cum-medicinal crop.
It is an annual plant, extensively cultivated as a food crop in India, the Mediterranean region, North Africa, and Yemen. Fenugreek seeds and herbs are well known for their distinct aroma and slightly bitter taste. The cultivation of this crop is confined to areas with moderate or low rainfall and a cool growing season without extreme temperatures. It can tolerate 10–15°C of frost (Duke 1986).
Fenugreek seed contains alkaloids including trigonelline, saponins, flavonoids, 4.4% protein, 86% moisture, 6% carbohydrate, 0.9% fat and 1.1% dietary fibers lipids, 360.0 mg calcium,167.0 mg sulphur, 76.1 mg sodium, 67.0 mg magnesium, 541 mg phosphorous, 51 mg potassium, 17.2 mg iron, 0.05 mg thiamin, 6450 IU vitamin ‘A’, 54 mg vitamin ‘C’, cellulose starch, ash, calcium, iron and β-carotene USDA (2001). Also it has been found to contain niacin, diosgenin (which are a compound that has properties similar to estrogen). Other active constituents in fenugreek are alkaloids, lysine and L-tryptophan, as well as steroidal saponins therefore it is used to in artificial flavoring and in the production of hormones. Green fenugreek is a good source of iron (Fe) as well as other minerals for human beings (Chhibba et al., 2000).

MATERIALS AND METHODS

In the present investigation ten genotypes of fenugreek (Trigonella foenum-graecum L.)were evaluated in Randomized Block Design (RBD)  at the Department of Horticulture, School of Agricultural Sciences, Career Point University, Kota (Rajasthan) during rabi season 2019-2020. The experimental materials consisting ten genotypes of fenugreek (Trigonella foenum-graecum L.)  i.e. RMt-305, RMt-303, RMt-351, RMt-305, RMt-361, RMt-1, RMt-354, RMt-143,AM-1, AM-1 and PARM-45. The experiment was laid out in a Randomized Block Design (RBD), with thirty treatments and three replications. Each genotypes was grown in a plot and plot size 7.92 m2. Each plot was grown in 30 cm row to row spacing and 10 cm plant to plant spacing. The observation was recorded on five randomly selected plants for nine-teen characters viz., germination percentage , plant height (cm) at 30,60 and 90 DAS, number of branches at 30, 60 and 90 DAS, number of leaves at 30 , 60 and 90 DAS, length internodes (cm), days taken to 50% flowering, days taken to maturity, fresh weight of plant (g),dry weight of plant (g), days to first pod formation,1000 seed weight (g),number of pods per plant, number of seeds per pod, pod length(cm),weight of pod (g),weight of seeds per pod (g),seed yield per plant (g), seed yield per plot (g), seed yield (q/ha-1).The data were estimated for variation among the genotypes analysis of variance was carried out suggested by Panse and Sukhatme (1995). Estimation of heritability in broad sense was done as per the formula given by Hanson et al. (1956) and the genetic advance (GA) was calculated by the following formula as suggested by allard (1960).

RESULT AND DISCUSSION

The analysis of variances for all the characters studied  have  been  presented  in  Table 1. Mean sum  of  squares  among  treatment  was  found significant for the characters viz. germination percentage, plant height (cm) at 30,60 and 90 DAS, number of branches at 30, 60 and 90 DAS, number of leaves at 30 , 60 and 90 DAS, length internodes (cm),days taken to 50% flowering, days taken to maturity, fresh weight of plant (g),dry weight of plant (g),days to first pod formation,1000 seed weight (g),number of pods per plant, number of seeds per pod, pod length(cm),weight of pod (g),weight of seeds per pod (g),seed yield per plant (g),seed yield per plot (g), seed yield (q/ha-1).
The  average  seed  yield  per  plot  was  274.72 g and  the  ranged  was  observed  to  be  219.56  to 383.89 (Table-2).  The  average  germination (%) was found to be 93.07%, where as germination  (%) ranged from 91.11to 95.33 %. The  average  plant  height at 90 DAS was  found  to be  59.11  cm,  where as  plant  height  ranged from   57.07   to   61.7   cm. The average days taken to 50% flowering was found to be 54.57 and the ranged was observed to be 49.4 to 57.07. The average length internodes (cm) was found to be 4.29 cm and the ranged was observed to be 3.5 to 5.83 cm. The average fresh weight of plant (g) was found to be 19.51g and the ranged was observed to be 17.47to 23.31g. The average days to first pod formation was found to be 12.02g and the ranged was observed to be 10.04 to 15.88g and all the other parameters the average and range of variation was high.
The phenotypic coefficient of variation (PCV) was higher to its corresponding genotypic coefficient of variation (GCV) for all the parameters under present study. High genotypic coefficient of variation was observed in weight of seeds per pod (25.38%), followed by seed yield (24.2%), number of pods per plant (20.77%). However, GCV was moderate for the characters such as seed yield per plant (16.78%), number of branches at 90 DAS (15.25%), number of leaves at 90 DAS (15.09%). Low genotypic coefficient of variation was observed for number of seeds per pod (10.63%), followed by 1000 seed weight (10.19%), fresh weight of plant (8.19%), plant height at 30 DAS (7.63%), plant height at 60 DAS (7.02%), days taken to maturity (6.02%) and high phenotypic coefficient of variation was observed in weight of seeds per pod (26.95%), followed by seed yield (25.37%), length internodes (24.31%), number of pods per plant (22.03%). However, PCV was moderate for the characters such as seed yield per plant (18.68%), number of branches at 90 DAS (16.65%), number of leaves at 90 DAS (16.18%). Low phenotypic coefficient of variation was observed for 1000 seed weight (12.19%), followed by  number of seeds per pod (12.04%), plant height at 30 DAS (10.50%), fresh weight of plant (9.87%), plant height at 60 DAS (7.57%), days taken to maturity (7.47%). These findings were quite similar to as reported by Verma (2003), Singh (2014) and Santhosh et al. (2017).
Heritability estimates in broad sense was high for seed yield (91.03), number of pods per plant (88.91), weight of pod (88.80), weight of seeds per pod (88.66), seed yield per plot (88.31), number of branches at 90 DAS (83.88), seed yield per plant (80.70), pod length (78.53), number of seeds per pod (77.98), days to first pod formation (70.88), length internodes (70.3). The findings were similar to findings of Patahk et al. (2014), Narolia etal. (2017) and Million et al. (2012).
Higher yield is the main breeding objective in all the crops but generally yield has moderate to low heritability. Yield is regarded as a complex parameter or super parameter, which is influenced by many component or contributing traits both in positive and negative direction. In the present investigation, expected genetic advance was recorded high with seed yield per plot (93.58), number of leaves at 90 DAS (17.78), number of pods per plant (16.82) and days taken to maturity (11.82). While medium values were observed for days taken to 50% flowering (6.09). Low genetic advance was recorded for seed yield (3.76), weight of seed per pod (3.56), weight of pod (3.55), seed yield per plant (3.14), number of branches at 90 DAS (2.87), fresh weight of plant (2.73), dry weight of plant (2.65), number of seeds per pod (2.42), pod length (2.28), germination percentage (1.6), plant height at 90 DAS (1.55), length internode (1.51). This is accordance with finding of Aman et al. (2018), Jain et al. (2013) and Japhet Singh (2014).
Heritability estimates along with the genetic advance are more useful than heritability alone in prediciting the resultant effect on selecting best individuals. In the present investigation, expected genetic advance expressed as percentage of mean was high for weight of seeds per pod (49.23%), seed yield (47.57%), dry weight of plant (22.06%), weight of pod (36.65%), length internodes (35.21%), seed yield per plot (34.06%), seed yield per plant (31.06%), number of leaves at 90 DAS (29.02%), number of branches at 90 DAS (28.77%), pod length (25.22%), dry weight of plant (22.06%) exhibited high genetic advance as percent of  mean. While medium values were observed for number of seeds per pod (19.34%), 1000 seed weight (17.56%), fresh weight of plant (24.02%), days taken to maturity (10.05%). Low genetic advance as percent of  mean was recorded for days to first pod formation (9.04%), days taken to 50% flowering (4.67%), plant height at 90 DAS (2.62%), germination percentage (1.72%). This is accordance with finding of Mamatha et al. (2017), Mahendra et al. (2016) and Lodhi et al. (2015).

Table 1: Analysis of variance for different characters in fenugreek

Source of variance

D.F.

Germination (%)

Plant height (cm)

No. of branches/plant

No. of leaves/plant

Length internodes (cm)

Days taken to 50% flowering

Fresh weight of plant (g)

Dry weight of plant (g)

Days taken to maturity

Days to first pod formation

Pod length (cm)

Weight of pod (g)

Weight of seeds / pod (g)

No. of pods/plant

No. of seed/pod

1000 seed weight (g)

Seed yield/ plant (g)

Seed yield/plot (g)

Seed yield (q/ha-1)

Replications

2

2.769

0.423

0.101

19.278

9.815

4.069

2.841

10.921

0.173

8.265

0.062

0.332

1.687

14.23

0.561

0.085

0.153

0.366

0.083

Treatment

9

6.618

8.179

7.414

269.64

176.65

14.978

8.826

8.418

2.618

42.066

5.137

10.512

10.562

234.41

5.830

3.863

9.356

7320.6

11.348

Error

18

2.171

3.194

0.446

12.731

26.215

4.484

1.150

1.129

0.323

5.065

0.429

0.423

0.431

9.354

0.501

0.484

0.690

309.25

6.493

 

 

 

 

 

Table 2: Mean value of genotypes, range, genotypic and phenotypic coefficient of variation, heritability in broad sense, genetic advance and genetic advance as % of mean for different characters in fenugreek

 

Characters

Grand Mean

Range

PCV %

GCV %

h2

GA (K=2.06)

GA (% of mean)

Mininum

Maximum

Germination percentage (%)

93.07

91.11

95.33

2.05

1.31

40.58

1.6

1.72

Plant height (cm) at 90 DAS

59.11

57.07

61.7

3.72

2.18

34.21

1.55

2.62

Number of branches at 90 DAS

9.99

8.49

13.14

16.65

15.25

83.88

2.87

28.77

Number of leaves at 90 DAS

61.29

50.22

83.42

16.18

15.09

87.05

17.78

29.02

Days taken to 50% flowering

54.57

49.4

57.07

5.17

3.42

43.82

2.55

4.67

Days taken to maturity

117.58

105.58

126.57

7.43

6.02

65.66

11.82

10.05

Length internodes (cm)

4.29

3.5

5.83

24.31

20.39

70.3

1.51

35.21

Fresh weight of plant (g)

19.51

17.47

23.31

9.87

8.19

68.98

2.73

14.02

Dry weight of plant (g)

12.02

10.04

15.88

15.69

12.96

68.25

2.65

22.06

Days to first pod formation

67.32

59.07

72.18

6.19

5.21

70.88

6.09

9.04

1000 seed weight (g)

10.40

9.22

12.71

12.19

10.19

69.92

1.82

17.56

Number of pods per plant

41.69

33.13

59

22.03

20.77

88.91

16.82

40.35

Number of seeds per pod

12.53

10.8

14.57

12.04

10.63

77.98

2.42

19.34

Pod length (cm)

9.06

7.73

11.56

15.59

13.81

78.53

2.28

25.22

Weight of pod (g)

9.71

7.5

13

20.03

18.88

88.80

3.55

36.65

Weight of seeds per pod (g)

7.24

5.04

10.52

26.95

25.38

88.66

3.56

49.23

Seed yield per plant (g)

10.12

8.23

13.83

18.68

16.78

80.70

3.14

31.06

Seed yield per plot (g)

274.72

219.56

383.89

18.72

17.59

88.31

93.58

34.06

Seed yield (q/ha-1)

7.90

5.47

10.86

25.37

24.2

91.03

3.76

47.57

 

Acknowledgments

I would like to express my very great appreciation to Mr Mukesh Kumar and Ms Asha Nama for his valuable and constructive suggestions during the planning and development of this research work.

REFERENCES

Aman, Kumar, V. P., Pandey, Maurya, V. K., D., Tiwari, & Sriom, (2018). Genetic variability, heritability & genetic advance in fenugreek (Trigonella  foenum-graecum L.). International Journal of Chemical Studies. 6(4),153-156.   
Allard, R.W., (1960). Principles of Plant Breeding. John Willey and Sons Inc., New York.
Chhibba, I. M., Kanwar, J. S. & Nayyar, V. K., (2000) .Yield and nutritive values of different varieties of fenugreek (Trigonella Spp.). Veg. Sci., 27, 176-179.
Duke, A. J., (1986). Handbook of legumes of world economic importance. New York: Plenum  Press.
Hanson, C.H., Robinson, H.F., & Comstock, R.E. (1956). Biometrical studies of yield in segregating populations of Korean, Lespedeza. Agronomy Journal, 48, 268-272.
Jain, A., Singh, B., Solanki, R. K., Saxena, S.N., & Kakani, R.K. (2013). Genetic variability and character association in fenugreek (Trigonella foenum- graecum L.). International Journal of Seed Spices. 3(2),22-28.
Japhet, S. (2014). Correlation co-efficient of component characters with seed yield and their effect in path analysis in fenugreek (Trigonella foenum- graecum L.)grown under six environmental conditions. Global Journal of Wood Science, Forestry and Wildlife. 2(1), 034-037.
Lodhi, P. S., Singh, P. P.,  Naruka, I.S., Kushwah, S. S., & Singh, A. K., (2015). Genetic variability, correlation and path analysis in fenugreek (Trigonella foenum-graecum L.). Indian Journal of Horticulture. 72(3), 429-433.
Mahendra, G., Naruka, I. S., & Shaktawat, R. P. S., (2016).Variability and correlation analysis in fenugreek (Trigonella foenum-graecum L.). Legume Research. 39(3), 459-465.
Mamatha, N. C., Tehlan, S. K., Srikanth, M., Ravikumar, T., Batra, V. K., Reddy, K. P. & Kumar, M. (2017). Variability studies for yield and its attributing traits in fenugreek (Trigonella foenum- graecum L.) genotypes,International Journal of Pure & Applied Bioscience. 5(3), 1075-1079.
Million, Fikreselassie, Habtamu Zeleke & Nigussie Alemayehu, (2012). Genetic variability of Ethiopian fenugreek (Trigonella  foenum-graecum L.) landraces. Journal of Plant Breeding and Crop Science. 4(3), 39-48.
Narolia, S. L., Meena, M. L., Atal, M. K., Verma, N., & Shivran, B. C., (2017). Character association and path analysis in fenugreek (Trigonella foenum–graecum L.). Green Farming. 8(5), 1089-1092.
Panse, V. G., & Sukhatme, P. V. (1995). Statistical Methods for Agricultural Workers, Revised Edition. ICAR, New Delhi.
Patahk, A. R., Patel, A. I., Joshi, H. K., & Patel, D. A. (2014). Genetic variability, correlation and path coefficient analysis in fenugreek (Trigonella foenum- graecum L.). Trends in Biosciences. 7(4), 234-237.
Santhosh, K. V., Gangadharappa, P. M., Vikram, H. C., Jagadeesha, R. C., & Chouhan, M., (2017). Correlation and path coefficient studies in fenugreek (Trigonella foenum-graecum L.) genotypes. Research in Environment and Life Sciences. 10(6), 572-574.
Singh, M. K. (2014). Genetic variability, heritability, genetic advance and correlation coefficient analysis in fenugreek (Trigonella foenum-graecum L.). HortFlora Res. Spectrum. 3(2), 178-180.
Verma, R., & Korla, B. N., (2003). Genetic variability in fenugreek (Trigonella foenum-graecum L.)  grown under mid-hills of Himachal Pradesh. Journal of Spices and Aromatic Crops. 12(1), 60-62.
USDA., (2001). Nutrient database for standard reference: Release 14. USDA, Washington, DC.




Photo

Photo