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Estimation of Genetic Variability and Diversity
Estimation of Genetic Variability and Diversity
E-ISSN: 2278-4136
P-ISSN: 2349-8234
www.phytojournal.com Estimation of genetic variability and divergence
JPP 2020; 9(2): 1890-1893
Received: 20-01-2020 in Greengram Vigna radiata (L.) germplasm
Accepted: 24-02-2020
(Rajasthan) and Agriculture Research Station, Badnapur al. (2009) [17] and Garje et al. (2014) [6]. The estimates of
(Maharashtra). The technique of random sampling was genetic advance as percent of mean was high for number of
adopted for recording the observations of 12 quantitative primary branches per plant (75.90) followed by number of
characters namely days to 50 percent flowering, days to clusters per plant (73.20) and pod length (69.30) Azam et al.
maturity, plant height, number of primary branches per plant, (2018) [3]. High heritability coupled with high genetic advance
number of clusters per plant, number of pods per plant, as percent of mean was observed for days to 50% flowering
number of seeds per pod, pod length, seed index, biological and number of clusters per plant. The high heritability is
yield per plant, harvest index and seed yield per plant. being exhibited due to favorable influence of environment
Recommended package of practices Were applied to raise a rather than genotype and selection for such traits may not be
healthy crop. Metric data on 12 characters were recorded at useful.
different stages of growth. Genetic divergence analysis are differed significantly with
The data collected on different characters were analyzed regard to characters studied and displayed marked divergence
through the method of analysis of variance for single factor when subjected to Wilk’s criteria taking all the 12 quantitative
(Gomez and Gomez, 1984) [8] and different genetic characters together. On the basis of magnitude of D 2 values,
parameters were estimated. Mahalanobis’s generalized hundred genotypes were grouped in 10 clusters (Table 3).
distance (D2) for genetic diversity. Grouping of genotypes Cluster II with 18 genotypes emerged as the largest cluster
into different clusters was done by using Tocher’s method as followed by cluster IV includes 17 genotypes, cluster VI
described by Rao (1952) [14]. The criterion used in clustering comprised 15 genotypes, and cluster X includes 1 genotype
by this method is that any two varieties belonging to the same (Fig. 1). The pattern of group constellation proved the
cluster should at least, on an average show a smaller D 2 existence of significant amount of variability. Wide diversity
values of the combinations of each genotype arranged in was also reported by Prasanna et al. (2013) [13] for 50
increasing (ascending) order of their magnitudes in a tabular greengram genotypes into eight clusters, Garje et al. (2013) [5]
form as described by Singh and Choudhary (1985) [15]. for 40 genotypes into 13 clusters, Ahmad et al. (2016) [1] for
35 genotypes into seven clusters, Chandra et al. (2017) [4]
Results and Discussion grouped 40 genotypes into seven clusters.
Hundred genotypes taken for analysis of variance showed Average intra cluster distance was ranged from 0.00 to 34.692
significant difference for all the characters studied (Table 1) maximum intra cluster distances were recorded for cluster VI
indicates that there is ample scope for selection of promising (34.692) followed by cluster IV (13), cluster IX (11.155)
genotypes from present germplasm for yield improvement. whereas minimum intra cluster distance recorded for cluster II
Maximum genotypic coefficient of variation (GCV) and (7.518) followed by cluster I (7.524) (Table 4). The inter
phenotypic coefficient of variation (PCV) was observed for cluster D2 value was maximum between cluster III and IV
number of primary branches per plant and number of clusters (1128.22) followed by cluster I and IV (1106.89), cluster II
per plant, while minimum genotypic variation was observed and IV (1102.97), cluster I and II (721.94) and cluster I and
for days to 50% flowering and days to maturity table 2. VI (626) while minimum inter cluster distance recorded for
Similar results were obtained by Lavanya (2006) [10], Kumhar cluster III and X (39). Suggesting that the genotypes present
and Chaudhary (2007) [9], and Sreethy (2017) [16]. The studies in these clusters may be used as parents for hybridization
on GCV and PCV indicated that the presence of high amount programme to develop desirable lines as heterosis can be best
of variation and role of the environment on the expression of exploited and chance of getting transgressive segregants are
these traits. The magnitude of PCV was higher than GCV for maximum when diverse genotypes are crossed.
all the characters which may be due to high degree of Cluster IV mean values showed maximum for the characters
interaction of genotypes with the environment. days to 50% flowering, days to maturity, plant height, number
All the characters showed high heritability percent in broad of pods per plant and seed yield per plant (Table 5). Similar
sense. Highest value of heritability was observed for protein findings were reported by Gokulkrishnan et al. (2012). On
content (98.80) followed by number of pods per plant (98.70) basis of seed yield performance and other specialized
and seed index (98.40) table 2. Similar results were reported characters genotypes KMII-584, KM-1413, COGG–10-10
by Pandiyan et al. (2006) [12] and Makeen et al. (2007) [11]. and BM-4 are identified that can be used for future breeding
The high heritability of these traits indicates that there is a programmes.
close correspondence between the genotype and phenotype The present investigation results indicate that considerable
and selection can be done. High estimates of genetic advance variability and diversity present in the experimental material
were noticed in character, plant height (22.20) followed by as hybridization programme involving genetically diverse
harvest index (19.80) and number of pods per plant (12.40) parents belonging to different clusters would provide an
whereas low estimates of genetic advance were observed for opportunity for bringing together gene constellations of
seed index (2.30) and pod length (2.60) table 2. The results diverse nature, promising hybrid derivatives probably due to
are in consonance with Makeen et al. (2007) [11], Yimram et complementary interaction of different genes in parents.
Table 4: Intra (diagonal) and inter cluster average distances (D2) for 12 different quantitative characters in greengram
3
Cluster I Cluster II Cluster III Cluster IV Cluster V Cluster VI Cluster VII Cluster VIII Cluster IX Cluster X
7.524 721.943 493.728 1,106.89 276.257 408.444 292.41 221.087 54.066
Cluster I 626 (25.026)
(2.743) (26.869) (22.223) (33.278) (16.621) (20.21) (17.108) (14.869) (7.353)
7.518 455.95 1102.97 293.88 603.291 205.176 311.381 198.61 41.770
Cluster II
(2.742) (21.353) (33.211) (17.143) (24.562) (14.324) (17.646) (14.077) (6.463)
1128.220 295.324 595.848 204.461 332.88 181.683
Cluster III 10.048 (3.17) 39 (6.245)
(33.589) (17.185) (24.41) (14.299) (18.245) (13.479)
294.465 616.975 105.616 296.287 216.972 49.984
Cluster IV 13 (3.606)
(17.162) (24.839) (10.277) (17.213) (14.731) (7.074)
9.734 606.242 252.778 320.052 229.825
Cluster V 43.56 (6.6)
(3.122) (24.622) (15.899) (17.893) (15.165)
8.236 242.736 355.322 207.072 41.107
Cluster VI
(2.878) (15.584) (18.851) (14.391) (6.413)
34.692 367.105 215.208 58.064
Cluster VII
(5.891) (19.169) (14.677) (7.623)
~ 1892 ~
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208.802 52.417
Cluster VIII 8.352 (2.891)
(14.455) (7.248)
11.155 79.21
Cluster IX
(3.345) (8.905)
Cluster X 0.000