Author:
Pratibha Sharma1*, Gouri Shankar Sahu2, Anita Mohanty3, Pradyumna Tripathy4, Neeraj Kumar1 and S. Karubakee5
Journal Name: Biological Forum, 17(6): 20-24, 2025
Address:
1Research Scholar, Department of Vegetable Science, Odisha University of Agriculture and Technology Bhubaneshwar (Odisha), India.
2Professor and Head, Department of Vegetable Science,Odisha University of Agriculture and Technology Bhubaneshwar (Odisha), India.
3Senior Vegetable Breeder and OIC, AICRP on Vegetable Crops, Odisha University of Agriculture and Technology, Bhubaneshwar (Odisha), India.
4Professor, Department of Vegetable Science, Odisha University of Agriculture and Technology Bhubaneshwar (Odisha), India.
5Research Scholar, Department of Agronomy, Odisha University of Agriculture and Technology Bhubaneshwar (Odisha), India.
(Corresponding author: Pratibha Sharma*)
DOI: https://doi.org/10.65041/BiologicalForum.2025.17.6.5
Bitter gourd, GCV, PCV, heritability, genetic advance.
Bitter gourd (Momordica charantia L.) is a popular cucurbitaceous vegetable crop belonging to family Cucurbitaceae, with 2n=2x=22 where immature fruits are eaten as vegetables. It is thought to be indigenous to tropical regions of Asia. In India, it is commonly referred to as 'karela'. The states of Eastern India i.e. Odisha, West Bengal, Assam, Jharkhand and Bihar may be considered as a probable primary centre of diversity of bitter gourd. It is an excellent source of vitamin B1, B2, B3, vitamin C, magnesium, potassium, calcium, phosphorous, manganese, folic acid, zinc, and has high dietary-fibre (Krawinkel and Keding 2006; Singla et al., 2023). It is rich in therapeutic qualities such as purgative, carminative, anti-diabetic, anthelmintic, antiemetic and anti-cancerous (Dhangar, 2024; Saha et al., 2024). Bitter gourd is cultivated round the year in Odisha and the vegetable also fetches a premium price in the market.
The Bitter gourd plants are monoecious annuals with medium size vines which are highly cross-pollinated crop in nature and such pollination mechanism can be used to generate hybrids because nature has a plethora of genetic variability. Given the varied agroclimatic conditions of Odisha, little is known about the genetic diversity and trait associations of bitter gourd genotypes. The presence of genetic variation in crops is necessary for their improvement as they respond to selection pressure. The extent to which the desirable characters are heritable and the magnitude of genetic variability already present in the genotype determines the effectiveness of any breeding program for the genetic improvement of quantitative characters. Therefore, the present investigation was carried out to study the presence of genetic variability, heritability and genetic advance among different bitter gourd genotypes.
The present investigation entitled “Evaluation of performance of Bitter gourd (Momordica charantia L.) genotypes under coastal conditions of Odisha” was carried out during the spring-summer season of the year, 2022 at the Horticultural Research Farm, OUAT, Bhubaneswar. The experiment was conducted in Randomized Block Design (RBD) in three replications with plot size of 3.0 × 2.7 m2. Each plot had three basins, and each basin had three plants. The 16 genotypes were used in the experiment, which were procured from AICRP on Vegetable Crops, OUAT. The cultural and management practices were implemented in accordance with the package of practices. Observations on fifteen quantitative characters namely days to first male flower opening, days to first female flower opening, days to 50% flowering, vine length, number of primary branches per vine, internodal length, leaf area, fruit length, fruit diameter, average fruit weight, number of fruits per vine, sex-ratio, fruit yield per vine, fruit yield per plot, and fruit yield per hectare and four morphological characters viz. fruit-color, ridges, presence of tubercles and shape of the fruit were recorded from five plants in each replication. The mean value was subjected to statistical analysis of variance (Panse and Sukhatme 1956). The phenotypic and genotypic coefficients of variation were computed as per Burton and De Vance (1953). The heritability in broad sense and genetic advance as percent mean (GAM) were determined by using the formula given by Lush (1949); Johnson et al. (1955) respectively.
Results of analysis of variance as presented in Table 1 showed significant differences among genotypes for all the 15 examined quantitative characters thereby suggesting existence of wide range of variations among the genotypes.
The widest range was recorded for average fruit weight (33.63g to 102.56g) followed by leaf area (128.96cm2 to 161.61cm2) and number of fruits per vine (11.76 to 24.03), indicating the presence of sufficient variability among the genotypes used in the present study thus, aiding in the selection of the best genotype from existing collection as presented in Table 2. The results contradicted the findings of Murlee et al. (2013), who found that yield per hectare had the greatest range of variation, followed by fruit weight, days to first appearance of the male flower, and fruit length. The general mean results indicated wide variation ranging from fruit yield per vine (1.03kg) to leaf area (144cm2). The genotypic variance ranged from 0.19 for fruit yield per vine to 378.57 for average fruit weight while, the phenotypic variance varied from 0.21 for fruit yield per vine to 397.66 for average fruit weight. In general all the values showed values parallel between these two variances showing higher values for the later than the former.
The study of data in Table 2 revealed that the estimates of phenotypic co-efficient of variation (PCV) was higher than the estimates of genotypic co-efficient of variation (GCV) for all the characters suggesting relative influence of environment on expression of different characters. Similar results were reported by Dey et al. (2009); Maurya et al. (2018); Talukder et al. (2018); Tyagi et al. (2018); Bhati et al. (2023); Sagar et al. (2024). The difference between PCV and GCV was very less in traits like average fruit weight, days to 50% flowering, fruit yield per plot, days to first female flower opening, sex-ratio, vine length, number of primary branches, days to first male flower opening, leaf area and number of fruits per vine indicating less environmental influence on these traits. Hence, these traits may be considered stable thus selection of such traits on phenotypic values may be considered rewarding. On the other hand traits like fruit length, internodal length, and fruit diameter relatively showed large differences among PCV and GCV indicating high environmental influence on expression of such characters. These results coincide similar with the results obtained by Singh et al. (2017); Kumanan et al. (2024) who reported close relation between PCV and GCV for almost all the characters whereas, Prasanth et al. (2020) reported close relation for number of fruits, fruit weight and fruit yield.
Heritability estimates provide the basis for selection of phenotypic performance but heritability estimated with genetic advance (GA) should always be considered simultaneously for obtaining an effective selection of characters in crop improvement programme (Johnson et al., 1955). In the current investigation (Fig. 1 & 2), high heritability coupled with high GA as percent of mean was recorded for characters like fruit yield per plot, average fruit weight, fruit yield per vine, sex-ratio, vine length, number of primary branches, number of fruits per vine, and fruit diameter indicating the predominance of additive components for these characters. Hence, direct selection through these characters would be more effective in future improvement programme. High heritability and low GA as percent of mean was observed for characters like days to 50% flowering, days to first female flower opening, leaf area indicating that non-additive gene effects were involved in the expression of these characters and that selection for such characters would not be rewarding. Characters such as days to first male flower opening, and internodal length showed moderate heritability and low GA as percent of mean suggesting that these characters are highly influenced by environment and selection for such characters would be less effective. Similar findings were reported by Dey et al. (2009); Pathak and Pahwa (2014); Rani et al. (2014); Rani et al. (2015); Maurya et al. (2018); Kumar et al. (2018); Talukder et al. (2018); Tyagi et al. (2018); Alekar et al. (2019); Prakash et al. (2021); Triveni et al. (2021); Nithinkumar et al. (2022); Bhati et al. (2023); Sagar et al. (2024).
In the present investigation, morphological characters like fruit color, ridges (continuous/discontinuous), presence of tubercles and shape of the fruit of all accessions were recorded (Table 3). The results revealed that genotypes BG-4 and BG-12 were green in color while genotype BG-9 was pale-green in color. However, genotypes like BG- 1, BG-2, BG-5, BG-13, BG-14 and BG-16 were light-green in color. Rests of the genotypes are dark-green in color. Genotypes BG-2, BG-8 and BG-10 showed continuous ridges while the rest other genotypes showed discontinuous ridges. The genotypes that showed continuous ridges also recorded absence of tubercles on their surface while, the rest of the genotypes showed tubercles presences on their fruit surface.
All the genotypes, based on fruit shape were categorized into three different shapes i.e. spindle, oblong and cylindrical. Among them, maximum number of genotypes had spindle-shaped fruits. However, three (BG-4, BG-6 and BG-16) genotypes had oblong-shaped fruits and four genotypes (BG-3, BG-7, BG-9 and BG-12) had cylindrical-shaped fruits.
Table 1: Analysis of variance for 15 characters of 16 genotypes of Bitter gourd.
Sr. No. | Characters | Mean Sum of Square | Calculated F | ||
Replication | Genotypes | Error | |||
Degree of freedom | 2 | 15 | 30 | ||
1. | Days to first male flower opening | 2.766 | 5.977 | 1.686 | 3.544* |
2. | Days to first female flower opening | 1.958 | 16.019 | 1.819 | 8.804* |
3. | Days to 50% flowering | 10.396 | 24.172 | 2.435 | 9.925* |
4. | Vine length (m) | 0.059 | 0.677 | 0.029 | 23.196* |
5. | No. of primary branches | 0.583 | 6.976 | 0.339 | 20.586* |
6. | Internodal length | 1.454 | 1.661 | 0.583 | 2.847* |
7. | Leaf area (cm2) | 663.029 | 296.555 | 53.405 | 5.552* |
8. | Fruit length (cm) | 0.909 | 11.139 | 2.769 | 4.022* |
9. | Fruit diameter (cm) | 0.030 | 1.012 | 0.181 | 5.583* |
10. | Avg. fruit weight (g) | 14.620 | 1154.817 | 19.089 | 60.497* |
11. | No. of fruits per vine | 43.895 | 45.335 | 2.533 | 17.900* |
12. | Sex-ratio | 11.089 | 20.489 | 0.861 | 23.801* |
13. | Fruit yield per vine (kg) | 0.104 | 0.595 | 0.018 | 32.713* |
14. | Fruit yield per plot (kg) | 0.158 | 23.609 | 0.296 | 79.875* |
15. | Yield/ha (t/ha) | 0.195 | 29.147 | 0.365 | 79.875* |
‘*’at 5% level ‘**’at 1% level
Table 2: Estimates of genetic parameters of different characters.
Sr. No. | Characters | Range | Mean | GV | PV | GCV (%) | PCV (%) | H (%) | GA | GAM | |
Min. | Max. | ||||||||||
1. | Days to first male flower opening | 36.89 | 41.56 | 39.45 | 1.43 | 3.12 | 3.03 | 4.47 | 45.90 | 1.67 | 4.23 |
2. | Days to first female flower opening | 45.56 | 54.22 | 48.20 | 4.73 | 6.55 | 4.51 | 5.31 | 72.23 | 3.81 | 7.90 |
3. | Days to 50% flowering | 51.33 | 61.67 | 55.50 | 7.24 | 9.68 | 4.85 | 5.61 | 74.84 | 4.80 | 8.64 |
4. | Vine length (m) | 1.81 | 3.22 | 2.54 | 0.22 | 0.25 | 18.28 | 19.48 | 88.09 | 0.90 | 35.34 |
5. | No. of primary branches | 6.67 | 11.33 | 9.15 | 2.21 | 2.55 | 16.26 | 17.47 | 86.72 | 2.85 | 31.20 |
6. | Internodal length | 7.31 | 9.85 | 8.26 | 0.36 | 0.94 | 7.26 | 11.75 | 38.11 | 0.76 | 9.23 |
7. | Leaf area | 128.96 | 161.6 | 144.0 | 81.04 | 134.4 | 6.25 | 8.05 | 60.28 | 14.4 | 9.98 |
8. | Fruit length (cm) | 9.45 | 16.93 | 13.29 | 2.79 | 5.56 | 12.57 | 17.75 | 50.19 | 2.44 | 18.35 |
9. | Fruit diameter (cm) | 2.64 | 4.41 | 3.46 | 0.27 | 0.45 | 15.23 | 19.58 | 60.45 | 0.84 | 24.39 |
10. | Avg. fruit weight (g) | 33.63 | 102.5 | 68.54 | 378.5 | 397.6 | 28.39 | 29.09 | 95.20 | 39.1 | 57.06 |
11. | No. of fruits per vine | 11.76 | 24.03 | 17.71 | 14.26 | 16.80 | 21.33 | 23.15 | 84.92 | 7.17 | 40.50 |
12. | Sex-ratio | 16.02 | 24.21 | 20.17 | 6.54 | 7.40 | 12.68 | 13.49 | 88.37 | 4.95 | 24.55 |
13. | Fruit yield per vine (kg) | 0.44 | 1.93 | 1.03 | 0.19 | 0.21 | 42.54 | 44.51 | 91.36 | 0.86 | 83.76 |
14. | Fruit yield per plot (kg) | 2.93 | 11.53 | 6.83 | 7.77 | 8.07 | 40.83 | 41.60 | 96.34 | 5.64 | 82.55 |
15. | Yield/ha (t/ha) | 3.26 | 12.81 | 7.59 | 9.59 | 9.95 | 40.83 | 41.60 | 96.34 | 6.26 | 82.55 |
Fig. 1. Growth and flowering characters.
Fig. 2. Yield and yield attributing characters.
Table 3: Variation in morphological features in bitter gourd.
Sr. No. | Genotypes | Fruit color | Ridges (Continuous/discontinuous) | Presence of tubercles | Shape of fruit |
1. | BG-1 | Light-green | Discontinuous | Present | Spindle |
2. | BG-2 | Light-green | Continuous | Absent | Spindle |
3. | BG-3 | Dark-green | Discontinuous | Present | Cylindrical |
4. | BG-4 | Green | Discontinuous | Present | Oblong |
5. | BG-5 | Light-green | Discontinuous | Present | Spindle |
6. | BG-6 | Dark-green | Discontinuous | Present | Oblong |
7. | BG-7 | Dark-green | Discontinuous | Present | Cylindrical |
8. | BG-8 | Dark-green | Continuous | Absent | Spindle |
9. | BG-9 | Pale-green | Discontinuous | Present | Cylindrical |
10. | BG-10 | Dark-green | Continuous | Absent | Spindle |
11. | BG-11 | Dark-green | Discontinuous | Present | Spindle |
12. | BG-12 | Green | Discontinuous | Present | Cylindrical |
13. | BG-13 | Light-green | Discontinuous | Present | Spindle |
14. | BG-14 | Light-green | Discontinuous | Present | Spindle |
15. | BG-15 | Dark green | Discontinuous | Present | Spindle |
16. | BG-16 | Light-green | Discontinuous | Present | Oblong |
The present study provides the basis of selecting superior bitter gourd genotypes based on genetic variability. Future research can focus on multi-location trials, molecular characterization and hybrid development. This will help in breeding high yielding, disease-resistant and region-specific varieties.
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