Legume Research

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Assessment of Yield-contributing Traits and Genetic Variability in Field Pea (Pisum sativum L.) under Heat Stress using Half-diallel Derived Genotypes

Aman Srivastava1, Shiva Nath1, Piyusha Singh1, Poonam Sharma2, Sonali Srivastava1, Anamish Tyagi1, Sujit Kumar Yadav3,*
  • 0009-0006-2816-2716, 0009-0006-2244-4982, 0009-0004-7095-4659, 0009-0004-4961-684X, 0009-0002-2666-8327, 0009-0008-8424-4606, 0000-0002-3898-3458
1Department of Genetics and Plant Breeding, Acharya Narendra Deva University of Agriculture and Technology, Kumarganj, Ayodhya-224 229, Uttar Pradesh, India.
2Department of Genetics and Plant Breeding, Chaudhary Sarwan Kumar Himachal Pradesh Krishi Vishvavidyalaya, Palampur-176 062, Himachal Pradesh, India.
3Department of Genetics and Plant Breeding, Swami Keshawanand Rajasthan Agriculture University, Bikaner-334 006, Rajasthan, India.
  • Submitted30-05-2025|

  • Accepted05-07-2025|

  • First Online 09-07-2025|

  • doi 10.18805/LR-5526

Background: The field pea is a vital, nutrient-dense and extremely productive cool-season legume crop that is planted all over the world and used for food, feed and fodder. Breeders can speed up the creation of robust, high-yielding cultivars by using half-diallel mating to choose superior parents and possible hybrids.

Methods: This study was conducted for analyzing the genetic variability on 55 field pea accessions, encompassing both parental line and there F1 progeny (hybrids) which were raised in late-sown conditions using a randomized block design (RBD) at the Genetics and Plant breeding Farm of Acharya Narendra Deva University of Agriculture and Technology, Ayodhya, Uttar Pradesh, India, over two successive Rabi seasons of 2022-23 and 2023-24. Data for eleven quantitative traits were collected by selecting five plants per plot randomly. ANOVA, PCV and GCV, broad sense heritability (h2b), genetic advance as a percentage of mean, path analysis and correlation coefficient were evaluated using statistical and biometrical methods to investigate the genetic diversity among the field pea genotypes.

Result: All traits showed a significant genetic variation, indicating scope for selection. All traits have higher PCV as compared to GCV, indicating environmental influences on their expression. Secondary branches/plant (27.838%) and primary branches/plant (21.005%) displayed the highest PCV values. Traits that showed significant variation across accessions had heritability ranging from 37.9% to 92.8%, suggesting low to high heritability. Seed yield per plant showed a positive correlation all traits except days to 50% flowering and days to maturity. A notable negative correlation was shown by seed yield plant-1 with days to 50% flowering and days to maturity. Path analysis identified biological yield, pods/plant, 100-seed weight and branches as having strong positive direct effects on yield, while days to flowering/maturity had negative direct effects. Based on these results, it is possible to enhance the yield components of late-sown peas by selecting for high biomass, pod number and seed weight.

Pulses are classified within the Leguminosae family and the Papilionoidea subfamily. Pulses are being produced in India’s semi-arid regions from ancient times. They are inexpensive and a reliable source of fibre, protein and phytochemicals. Legumes have been recognized as an important resource of food in the diet of human, decreasing the risk of heart disease and cancer because of their composition that makes it suitable for human consumption (Carbas et al., 2023). Field pea belongs to dicotyledons class with the chromosome number of 2n=14. It is extensively cultivated in cooler climates and is native to Southwestern Asia. Even though it is a self-pollinating crop, which precludes a significant amount of gene flow, the Pisum genus is the origin of many viable wild crosses, due to which there is sufficient variation within the species (Jing et al., 2010).  Since it is primarily a cold-weather crop, it can endure light frost. Field pea and garden pea are the two types of peas grown traditionally all around the globe. One of the many uses for field peas is as a green manure, straw, immature grain, silage, haylage, forage dry matter and green fodder (Ravindran et al., 2010). Field pea contribution in India is about 3% of the overall area used for pulses and approximately five percent of the entire quantity produced. Previous studies show that crops grown under heat stress conditions tend to reduce yield by 18 to 33 per cent (Lamichaney et al., 2021). Temperature sensitivity of field pea (cold-season legumes) is greater than warm season legumes (Hall, 2001). Moreover, field peas are relatively low heat-tolerant compared to chickpeas and lentils (Siddique, 1999) and therefore their production often decreases when the day temperature at the time of flowering go beyond 25°C (Guilioni et al., 2003; Sadras et al., 2013). In this article, we examine the variability and correlation among F1s and their parents, while analysis of heterosis and combining ability will be reported in a distinct paper. By the year 2100, the optimum temperature will increase from 2-4 degrees celsius (IPCC, 2007). The field pea cultivars which are under late-sown condition, there is a substantial loss in yield due to terminal heat stress. (Lamichaney et al., 2021). Since cool-season legumes growth and development processes are greatly impacted by high ambient temperatures, it is anticipated that seed quality will be impacted as well. High temperatures can have a negative impact on seed growers, since the seed requirements of field pea are higher. This research analyses the variability, association and path coefficient analysis of yield components of the accessions of field pea under heat stress environment.
The trial was conducted over two consecutive Rabi seasons. In the first year (2022-23), ten genetically diverse field pea lines were evaluated under randomized block design (RBD) and used to generate 45 F hybrids following a half-diallel mating design (Griffing et al., 1956). In the following season (2023-24), these F1s, along with their 10 parents, were evaluated under late-sown conditions using an RBD with three replications. The formula for crosses was:
 
P(p-1)/2
‘p’ denotes = No. of parents
       
Forty five F1s and ten parental lines (PANT P-347, PANT P-200, RFP 2009-2, IPFD 18-14, PANT P-243, VL-47, IPF14-13, IPF 14-16, RILHE-2 and HFP-1802) are selected based on genetic diversity and accession were grown using a randomized block design (RBD) in Rabi season during November 2022-23 and 2023-24 in late-sown or heat stress conditions at the Genetics and Plant Breeding Farm of Acharya Narendra Deva University of Agriculture and Technology in Ayodhya, Uttar Pradesh, India, for optimal crop growth. Genotypes were grown in 3 replications for the study of eleven traits viz., days to 50% flowering, days to maturity, secondary branches/plant, primary branches/plant, plant height, pods/plant, seeds /pod, harvest index (%), 100-seed weight (g), biological yield/plant (g) and seed yield/plant (g). Collection of data was done by selecting five plant/plot randomly. Different biometrical and statistical measures, including GCV and PCV (Burton, 1953), ANOVA (Panse and Sukhatme, 1954), genetic advance (Johnson et al., 1955), Broad sense heritability (h2b) (Allard, 1960), path coefficient (Dewey, 1959) and trait correlation (Searle, 1961) were evaluated.
Anova, GCV and PCV
 
The analysis of variance (ANOVA) for all 11 morpho-agronomic traits in late-sown field pea revealed highly significant differences among genotypes (both parents and half-diallel crosses), demonstrating substantial genetic variation within the experimental material (Table 1). When comparing parents versus hybrids, significant differences were observed for all traits except seed per pod, indicating that hybridization effectively enhanced most agronomic characteristics. This genetic diversity provides a solid foundation for effective selection and breeding programs. The inference drawn from Table 2 showed that PCV were higher than the GCV for all traits, showing environmental influence on the trait expression. Secondary branches/plant (27.838%) and primary branches/plant (21.005%) displayed the maximum values of PCV, trailed by seed yield plant-1 (20.42%).

Table 1: Anova of half-diallel crossings and parents for 11 field pea traits under late-sown condition.



Table 2: Mean and range of variability of parents and half-diallel crosses for 11 characters of field pea in late sown condition.


       
Similarly, the highest GCV values were found for secondary branches/plant at 23.85%, trailed by seed yield/plant at (19.51%) and biological yield/plant (18.52%). Days to maturity has the lowest GCV (5.198%) and PCV (7.440%,) values, respectively. Consistent with Jeberson et al., (2016), Afreen et al., (2017) and Meena et al., (2017). The narrow gap between GCV and PCV values for traits such as biological yield per plant and plant height suggests these characteristics are less influenced by environmental fluctuations and are primarily under genetic control. Conversely, traits showing wider GCV-PCV gaps, such as harvest index, indicate greater environmental sensitivity and may require more careful management during selection.
 
Heritability and genetic advance
 
Heritability for all traits ranges from 37.9% to 92.8%, suggesting low to high heritability. The largest heritability trait is biological yield per plant (92.8%), followed by plant height (91.6%), seed yield per plant (91.22%), pod per plant (89.4%), seed per pod (76.5%), secondary branches per plant (73.4%) and 100-seed weight (62.2%). Days to 50% flowering (55.4%) has shown moderate heritability, followed by days to maturity (48.8%) and primary branches per plant (41.04%), while harvest index (37.9%) has the lowest heritability. Higher heritability estimates suggest that genetic factors influenced these traits. Biological yield/plant had the largest genetic advance (GA), at 35.10%, followed by plant height (29.40%) and seed yield per plant (13.25%). The range of genetic advance was 0.50% to 35.10%. These results are in agreement with the findings of Afreen et al., (2017) and Pratap et al., (2024) who reported significant variability for all traits including 100-seed weight, plant height, pods per plant and primary branches per plant in pea. Similarly, Singh et al., (2019) and Gebre et al., (2024) concluded that traits with high heritability and high genetic advance are most amenable to breeding improvement. The present study confirms that biological yield per plant, seed yield per plant and plant height possess the most favorable genetic parameters for effective selection and breeding improvement in field pea under late-sown conditions.Traits exhibiting high heritability but low genetic advance may be governed by non-additive gene effects, while traits with low heritability and low genetic advance are highly influenced by environmental factors and are difficult to improve through direct selection. For such traits, indirect selection through correlated characters or selection in controlled environments would be more effective.
 
Correlation coefficient and path analysis
 
The perusal of Table 3 and 4 showed a wide similarity among the traits. This pattern is consistent with the findings of Singh et al., (2017) and Iqbal et al., (2020). The higher genotypic correlations suggest that the true genetic relationships between traits are stronger than what appears phenotypically, emphasizing the importance of considering genetic correlations in breeding decisions. Positive correlation was found among seed yield/plant and all traits except days to 50% flowering and days to maturity. Days to 50% flowering and days to maturity were significantly negatively correlated with seed yield plant-1. This relationship can be attributed to the fact that early maturing genotypes escape terminal heat stress and moisture stress commonly encountered in late-sown conditions, thereby maintaining higher productivity. Similar observations were reported by Katoch et al., (2016), Tasnim et al., (2022) and Yadav et al., (2024). Primary branches plant-1 were significantly positively associated with seed yield per plant, harvest index, plant height and 100-seed weight, showing that more primary branches increase the components of seed yield and overall yields. Secondary branches/plant were significantly positively associated with pod/plant, biological yield/plant, 100-seed weight and seed yield/plant. In the trait plant height, there is a positive and significant relationship with seeds/pod, seed yield per plant, harvest index and primary branches per plant, showing that taller plants typically produce more seeds and produce a more yield. A significant positively correlation between pods/plant and 100-seed weight, secondary branches/plant, biological yield/plant, primary branch/plant and seed yield/plant, signifying that pods/plant plays an important role in improving seed yield and overall yield.

Table 3: Genotypic correlation of parents and their half-diallel crosses for 11 characters in field pea under late sown condition.



Table 4: Phenotypic correlation of parents and their half-diallel crosses for 11 characters in field pea under late sown condition.


       
The seed pod-1 was significantly correlated with plant height, biological yield/plant, seed yield/plant and harvest index, suggesting that increase in seed/pod positively affect overall seed yield. A positive correlation was found between 100-seed weight and biological yield/plant, pods/plant, primary branches/plant, number of secondary branches/plants, harvest index and seed yield plant-1, indicating that increase in this trait can result in increased yield. Biological yield/plant is correlated positively with its seed yield, pod/plant, secondary branches/plant, seed pod-1 and 100-seed weight demonstrating that biomass enhancement can increase overall yield. Seed yield/plant, seed pod-1, primary branches/plant, plant height and 100-seed weight all have positive correlations with harvest index, indicating that a higher harvest index leads to a higher total yield component. These trait associations are in agreement with the results of Ali et al., (2019) and Jeberson et al., (2016), Katoch et al., (2021) who reported similar correlation patterns in field pea. The consistent positive correlations observed across studies indicate the reliability of these relationships and their potential exploitation for indirect selection to improve seed yield, particularly focusing on pods per plant and 100-seed weight, as suggested by Srivastava et al., (2018), Georgieva et al., (2015) and Sharma et al., (2023). Seed yield was strongly and significantly positively correlated with pods/plant (r » 0.83) and 100-seed weight (r » 0.74) and negatively with days to flowering/maturity. By concentrating on these traits, breeders can increase field pea production, particularly in light of changing climates. Bhuvaneswari et al., (2017) and Lal et al., (2018) had similar findings. Fig 1 demonstrate correlation heatmap of 11 traits in field pea showing relationship among variables. Correlation coefficients reveal trait relationships, without demonstrating causation. Phenotypic path coefficient analysis partitions correlation coefficients into direct and indirect effects with seed yield as the dependent variable. Table 5 shows that biological yield (0.8698) has the highest direct positive effects on seed yield, suggesting that it is a primary driver of seed yield, indicating importance selecting high biomass. Pods/plant (0.7649), 100-seed weight (0.6169), secondary branches/plant (0.6084), harvest index (0.3731), seed/pod (0.3197), primary branches/plant (0.2711) and plant height (0.2253) were the next most positive direct effects on seed yield. These findings were also reported Tiwari and Lavanya, (2012), Basaiwala et al., (2013) and Kumar et al., (2013). Characters’ indirect contributions to seed yield were extremely minimal and detrimental. Days to 50% flowering (-0.1842) and days to maturity (-0.3148) showed a significant negative direct effect. By biological yield per plant, strong indirect impacts were observed in the no. of pods/plant (0.5968), secondary branches plant-1 (0.5491), 100-seed weight (0.4366) and seeds per pod (0.1273). This indicates that these traits influence seed yield through two pathways: directly through their own effects and indirectly by enhancing total biomass production, which subsequently translates to higher seed yields. The substantial indirect effects through biological yield demonstrate that traits contributing to vegetative vigor ultimately benefit seed production. This finding aligns with Tofiq et al., (2015), who demonstrated that biomass increase is strongly associated with higher seed yield.

Fig 1: Correlation heatmap of 11 traits in field pea showing relationship among variables.



Table 5: Phenotypic path matrix of parents and their half-diallel crosses for 11 characters in field pea under late sown condition.

Significant genetic diversity was found in the plant height, days to 50% flowering, days to maturity and number of pods per plant for late-planted field pea half-diallel crosses, according to the analysis of variance (ANOVA). More phenotypic variance than genotypic variation was discovered in the study, indicating that the environment influences how traits are expressed. High PCV and GCV values were found for the number of secondary branches plant-1, which can be used to optimize the breeding program. Plant height and biological yield plant-1 showed high heritability coupled with high genetic advance, suggesting traits can be enhanced by breeding and selection. This implies that selection can enhance these traits and that heredity has a significant impact on them. Correlation research demonstrated the significance of variables such as harvest index, pods per plant and 100-seed weight in field pea breeding initiatives aimed at increasing output. According to path coefficient analysis, 100-seed weight, biological yield, harvest index, pods/plant and secondary branches/ plant all directly increase seed yield/plant, demonstrating their worth. The results suggest that field pea output can be increased by choosing key agronomic traits which can be helpful in increasing its productivity.
The present study was supported by the department of Genetics and Plant Breeding, Acharya Narendra Deva University of Agriculture and Technology, Kumarganj, Ayodhya which provided the genotypes used in this research.

Disclaimers
 
The authors present only their findings and do not represent any affiliated organizations. In the case of direct or indirect losses resulting from the use of this content, the authors accept responsibility for its accuracy and quality.
 
Informed consent
 
No animal used during the research.
Neither author has a conflict of interest. No funding or sponsorship was involved in the design or article preparation.

  1. Afreen, S., Singh, A.K., Moharana, D.P., Singh, V., Singh, P. and Singh B. (2017). Genetic evaluation for yield and yield attributes in garden pea (Pisum sativum var. hortense L.) under north Indian gangetic plain conditions. Int.J. Curr. Microbiol. App. Sci. 6(2): 1399-1404.

  2. Ali, I., Mahmood, M.T., Akhtar, M.I., Zafar, A., Khan, A.M., Zubair, M. and Anum,W. (2019). Some direct and indirect selection indices for increased yield of peas (Pisum sativum L.). J. Environ Agric Sci. 21: 23-28.

  3. Allard, R.W. (1960). Principles of Plant Breeding. John Willey and Sons. Inc. New York, p 485.

  4. Basaiwala P., Rastogi N.K. and Parikh M. 2013.Genetic variability and character association in field pea (Pisum sativum L.) genotypes. Asian Journal of Horticulture. 8(1): 288-29.

  5. Bhuvaneswari, S., Sharma, S.K., Punitha, P., Shashidhar, K.S., Naveen kumar, K.L. and Prakash, N. (2017).Evaluation of morphological diversity of field pea [Pisum sativum subsp. arvense (L.)] germplasm under sub-tropical climate of Manipur. Legume Research. 40(2): 215-223. doi: 10. 18805/lr.v0iOF.10756

  6. Burton, G.W. and Devane, D.E. (1953). Estimating heritability in tall fescue (Festuca arundinacea) from replicated clonal material 1. Agronomy Journal. 45(10): 478-481.

  7. Carbas, B., Machado, N., Pathania, S., Brites, C., Rosa, E.A. and Barros, A.I. (2023). Potential of legumes: Nutritional value, bioactive properties, innovative food products and application of eco-friendly tools for their assessment. Food Reviews International. 39(1): 160-188.

  8. Dewey, D.R. and Lu, K. (1959). A correlation and path coefficient analysis of components ofcrested wheatgrass seed production. Agronomy Journal. 51(9): 515-518.

  9. Gebre, W., Mekbib, F., Tirfessa, A. and Bekele, A. (2024). Genetic diversity, association and path coefficient analyses of sorghum [Sorghum bicolor (L.) Monech] genotypes. Scientifica. (1): 1611869.

  10. Georgieva, N., Nikolova, I. and Kosev, V., (2015). Association study of yield and its components in pea (Pisum Sativum L.). International Journal of Pharmacognosy (IJP). 2(11):  536-542.

  11. Griffing, B.R.U.C.E. (1956). Concept of general and specific combining ability in relation to diallel crossing systems. Australian Journal of Biological Sciences. 9(4): 463-493.

  12. Guilioni, L., Wéry, J. and Lecoeur, J. (2003). High temperature and water deficit may reduce seed number in field pea purely by decreasing plant growth rate. Funct. Plant Biol. 30: 1151-1164. 

  13. Hall, A.E. (2001). Crop Responses to Environment. Boca Raton, FL: CRC Press.

  14. IPCC, (2007). Summary for policymakers, in The Physical Science Basis: Contribution of working group I to the fourth assessment report of the intergovernmental panel on Climate Change, eds S. Solomon, D. Qin, M. Manning, Z. Chen, M. Marquis, K.B. Averyt, et al. (Cambridge: Cambridge University Press), 2-4.

  15. Iqbal, M., Najeebullah, M., Nadeem, K., Chishti, S.A.S., Hammad, G., Shabbir, R.H., Nabi, G., Zubair, M., Qadeer, Z., Shahzad,  U. (2020). Association pattern among yield and its related attributes for early peas (Pisum sativum L.). International Journal of Biosciences. 16(3): 83-87.

  16. Jeberson, M.S., Shashidhar, K.S. and Iyanar, K. (2016). Estimation of genetic variability expected genetic advance, correlation  and path analysis in field pea (Pisum sativum L.). Elect. J. Plant Breed. 7(4): 1074-1078.

  17. Jing, R., Vershinin, A., Jacek, G., Paul, S., Petr, S., David, F.M., Mike,  A., Neol, E. and Andrew, J.F. (2010). The genetic diversity  and evolution of field pea (Pisum sativum L.) were studied by high-throughput retrotransposon-based insertion polymorphism (RBIP) marker analysis. BMC Evolutionary Biology. 10(1): 44.

  18. Johnson, H.W., Robinson, H.F. and Comstock, R.E. (1955). Estimates  of genetic and environmental variability in soybeans. Agronomy Journal. 47(7): 314-318.

  19. Katoch, V., Rathour, R., Sharma, S., Rana, S.S. and Sharma, A. (2021). Studies on genetic parameters, correlation and path coefficient analysis in er2 introgressed garden pea genotypes. Legume Research-An International Journal. 44(6): 621-626. doi: 10.18805/LR-4142.

  20. Katoch, V., Singh, P., Devi, M.B., Sharma, A., Sharma, G.D. and Sharma, J.K. (2016). Study of genetic variability, character  association, path analysis and selection parameters for heterotic recombinant inbred lines of garden peas (Pisum sativum var. hortense L.) under mid-hill conditions of Himachal Pradesh, India. Legume Research-An International  Journal. 39(2): 163-169. doi: 10.18805/lr.v0iof.6775.

  21. Kumar, B., Kumar, A., Singh, A.K. and Lavanya, G.R. (2013). Selection  strategy for seed yield and maturity in field pea (Pisum sativum L. arvense). African Journal of Agricultural Research. 8(44): 5411-5415.

  22. Lal, K., Kumar, R., Singh, V., Chaudhary, A.K., Yadav, H. and Kumar, A. (2018). Evaluation of genetic divergence for grain yield and its contributing traits in field pea (Pisum sativum L. var. arvense) Int. J. of Curr. Microbiol. App. Sci. 7(6): 1821-1826.

  23. Lamichaney, A., Parihar, A.K., Hazra, K.K., Dixit, G.P., Katiyar, P.K., Singh, D. and Singh, N.P. (2021). Untangling the influence of heat stress on crop phenology, seed set, seed weight and germination in field pea (Pisum sativum L.). Frontiers in Plant Science. 12: 635868.

  24. Meena, B.L., Das, S.P., Meena, S.K., Kumari, R., Devi, A.G. and Devi, H.L. (2017). Assessment of gcv, pcv, heritability and genetic advance for yield and its components in field pea (Pisum sativum L.) Int. J. Curr. Microbial. App. Sci6(5): 1025-1033.

  25. Panse, V.G. and Sukhatme, P.V. (1954). Statistical methods for agricultural workers. Indian Council of Agricultural Research. New Delhi. xvi + 361 pp.

  26. Pratap, V., Sharma, V. and Shukla, G. (2024). Assessment of genetic variability and relationship between different quantitative traits in field pea (Pisum sativum var. arvense) germplasm. Legume Research. 47(6): 905-910.

  27. Ravindran, G., Nalle, C.L., Molan, A. and Ravindran, V. (2010). Nutritional  and biochemical assessment of field peas (Pisum sativum  L.) as a protein source in poultry diets. Poultry Science Journal. 47(1): 48-52.

  28. Sadras, V.O., Lake, L., Leonforte, A., McMurray, L.S. and Paull, J.G. (2013). Screening field pea for adaptation to water and heat stress: associations between yield, crop growth  rate and seed abortion. Field Crops Res. 150: 63-73. 

  29. Searle, S.R. (1961). Phenotypic, genetic and environmental correlations. Biometrics. 17(3): 474-480.

  30. Sharma, S., Bhushan, A., Samnotra, R.K., Kumar, B., Wani, O.A., Naik, R. and Kumar, M. (2023). Genetic variability, correlation  and path coefficient analysis in advanced matromorphic generations of garden pea (Pisum sativum L.). Legume Research-An International Journal. 1(7). doi: 10.18805/ LR-5128.

  31. Siddique, K. (1999). Abiotic Stresses of Cool-Season Pulses in Australia. Perth, WA: Centre for Legumes in Mediterranean  Agriculture and University of Western Australia.

  32. Singh, N. (2017). Pulses: An overview. J Food Sci Technol. 54(4): 853-857.

  33. Singh, S., Verma, V., Singh, B., Sharma, V. R. and Kumar, M. (2019).  Genetic variability, heritability and genetic advance studies in pea (Pisum sativum L.) for quantitative characters. Indian Journal of Agricultural Research. 53(5): 542-547. doi: 10.18805/IJARe.A-5245.

  34. Srivastava, A., Sharma, A. and Kumar, R. (2018). Cluster analysis in field pea (Pisum sativum L.). Journal of Pharmacognosy and Phytochemistry. 7(5): 655-657.

  35. Tasnim, S., Poly, N.Y., Jahan, N. and Khan, A.U. (2022). Relationship of quantitative traits in different morphological characters of pea (Pisum sativum L.). J. Multidisc. Appl. Nat. 2(2): 103-114.

  36. Tiwari, G. and Lavanya, G.R. (2012). Genetic variability, character association and component analysis in F4 generation of field pea (Pisum sativum var. arvense L.). Karnataka Journal of Agriculture Science. 25(2): 173-175.

  37. Tofiq, S.E., Abdul Khaleq, D.A., Amin, T.N.H. and Azez, O.K. (2015). Correlation and path coefficient analysis in seven field pea (Pisum Sativum L.). Genotypes created by half-diallel  analysis in Sulaiman region for f2 generation. International Journal of Plant, Animal and Environmental Sciences. 5(4): 93-97.

  38. Yadav, A., Nath, S., Bharti, B., Singh, S., Yadav, S., Bhardwaj, R. and Yadav, S.K. (2024). Genetic variability studies in chickpea (Cicer arietinum L.) for yield and contributing traits through half-diallel mating strategy under late-sown conditions. Legume Research-An International Journal. 47(12): 2042-2048. doi: 10.18805/LR-5391.

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