Study of variability in pod characteristics of indigenous tamarind (Tamarindus indica L.) genotypes
Abstract
A total of 42 indigenous tamarind (Tamarindus indica L.) genotypes were thoroughly assessed across various villages in seven blocks of Surguja district of Chhattisgarh, during the year 2022–23 and 2023–24. The objective of the study was to determine the degree of variation present in pod characters among the genotypes, in order to identify elite accessions worth pursuing for improvement and conservation program. A Randomized Block Design (RBD) comprising four replications was used for the study and the resulting data were subsequently analysed. Results revealed that STAM-9 recorded the highest mature pod weight (32.88 g), mature pod length (16.85 cm) and pulp weight per pod (16.86 g), reflecting its superiority for improving overall pod yield. The widest pod was recorded in STAM-40 (2.84 cm), whereas STAM-15 exhibited the maximum pod thickness (1.8 cm). Minimum shell weight per pod (1.41 g) was noted in STAM-1, and the lowest fibre weight per pod (0.18 g) was recorded in STAM-26.
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Introduction
Tamarindus indica L. commonly known as tamarind, is a slow-growing, multipurpose, evergreen, tropical tree species, widely distributed across the tropical and subtropical regions of the world. Tamarind is a hardy monotypic tree which belongs to the family Leguminosae and has chromosome number, 2𝑛 = 24 (Purseglove, 1981). The word 'tamarind' is believed to have originated from the Arabic phrase "Tamar-e-Hind" meaning "Date of India" (Morton, 1987; Mishra, 1997) [2,1] . Tamarind is native to the tropical regions of Africa, with its natural distribution extending from Sudan, Ethiopia, Kenya, and Tanzania in the east, across the sub-Sahel belt, to Senegal in the west (Brandis, 1921; Ridley, 1922; Dalziel, 1937; Irvine, 1961) [3,4,5,6] . Tamarind cultivation in India is predominantly concentrated in the states of Tamil Nadu, Andhra Pradesh, Kerala, Chhattisgarh, and Madhya Pradesh. Tamarind demonstrates a high degree of adaptability to diverse soil conditions. In India, it exhibits considerable tolerance to sodic and saline soils and also plays a role in controlling soil erosion (Das et al., 2001) [7] . In most countries where tamarind is cultivated, the harvesting season generally spans February to April, with occasional extension up to June. The fruit takes the form of a pod, 5-16 cm long and about 2 cm broad, oblong in shape, curved or straight and rounded at the ends. It is enclosed by a light grey or brown, scaly epicarp, within which lies a firm but soft, thick, reddish-brown pulp. The pulp is traversed by seed cavities containing the seeds and comprises tough, branched fibres running along its outer surface from base to apex. The seed consists of two main components, the seed coat and the kernel (George et al., 1993) [8] . Among the various parts of the tamarind tree, the fruit pulp holds the greatest economic value, finding wide application in domestic and industrial food processing as well as in medicinal use. The ripe pulp, especially of the sweet-type tamarind, is commonly eaten in its fresh form, whereas both sour and sweet pulps serve as key ingredients in numerous processed products such as desserts, pickles, jams, candies, juices, porridges and drinks (Jayaweera, 1981) [9] . Despite being an economically significant tree crop of India, tamarind has received relatively limited research attention aimed at its scientific understanding and improvement as a commercial crop. At present, tamarind is cultivated across the country, with the majority of trees being of seedling origin. Being a highly cross-pollinated and seed-propagated species, tamarind exhibits considerable variation within its populations. Individual trees frequently display marked genetic diversity even within the same population, underscoring the heterogeneous nature of the crop (Rajamanickam, 2020) [10] . The extensive variation evident in characters such as foliage, flowering, pod production and timber quality indicates considerable potential for genetic improvement of the crop. Such improvement is fundamental to increasing the productivity and yield of tamarind and involves developing genotypes that combine desirable traits, including growth habit, high yield potential and resistance or tolerance to major pests, diseases and drought stress (Radhamani et al., 1998) [11] . This variability may arise from genetic causes, environmental factors, or a combination of both.
Estimating the level of variability for each trait, in quantitative terms, helps in understanding the potential of a given tree and the feasibility of improving desirable and economically valuable characters through selection. Insights into the nature and extent of variation, together with the association between different traits and yield, are useful tools for identifying and selecting superior tamarind genotypes.
Materials and methods
The present investigation comprised 42 tamarind (Tamarindus indica L.) genotypes procured from seven blocks of Surguja district, Chhattisgarh, namely Ambikapur, Batauli, Lakhanpur, Udaipur, Lundra, Mainpat and Sitapur. Geographically, Surguja district is situated in the northern part of Chhattisgarh between 22°19′ N to 24°6′ N latitude and 81°34′ E to 84°4′ E longitude, at a mean altitude of 623 m above mean sea level. Genotypes exhibiting distinct morphological variation and fruiting characteristics were purposively selected for evaluation.
Result and discussion
Variability in pod characteristics
Significant variations were found between the tamarind genotypes marked in the current study based on observations of mature pod length (cm), which are compiled in It is evident from the result obtained under the present investigation that the various genotypes showed variation with respect to mature pod length of tamarind. Among the various genotypes, the maximum mature pod length (16.85 cm) was measured under the genotypes STAM-9, while the minimum mature pod length (3.46 cm) was recorded by STAM-26 in pooled analysis under present investigation. Diversity in mature pod length in tamarind genotypes might be due to genetic factor which govern fruit development and efficiency of nutrient translocation during pod formation. Such kinds of differences in fruit length reported by Shukla (2006) [12] , Praveenakumar et al. (2020) [13] and Mishra (2021) [14] in tamarind genotypes.
Significant variations were found between the tamarind genotypes observed in the current study based on observations of mature pod width (cm), which are compiled in Table 1 and visually depicted in Fig. 2.
Throughout the first year of the study, it was registered that the mature pod width of tamarind genotypes ranged from 1.9 cm (STAMIt is evident from the result obtained under the present investigation that the various genotypes showed variation with respect to mature pod width of tamarind fruits. Among the various genotypes, the maximum mature pod width (2.84 cm) was measured under the genotypes STAM-40, while the minimum mature pod width (1.88 cm) was recorded by STAM-15 in pooled analysis under present investigation. The difference in pod width among the genotypes might be due to genetic factors controlling fruit shape and fruit development.
Differences in cell division and expansion during pod growth also contributes to pod width variation. The results are in close agreements with the findings of Biradar (2001) [15] , Prabhushankar (2001) [16] and Mishra (2021) [14] in tamarind genotypes.
The observations regarding thickness of pod (cm) of tamarind genotypes showed significant differences among the different genotypes observed under present investigation, which are summarized in Table 1 and graphically shown in Fig. 1, it can be concluded that various genotypes showed variation with respect to thickness of pod of tamarind fruits. Among the various genotypes, the maximum thickness of pod (1.8 cm) was measured under the genotypes STAM-15, while the minimum thickness of pod (0.97 cm) was recorded by STAM-42 in pooled analysis under present investigation. Variation in the thickness of pod in tamarind genotypes might be due to the genetic factors influencing pod wall development and lignification. Pod thickness depends on the degree of cell wall expansion and hardening during the fruit maturation phase. Environmental factors such as soil nutrient levels and water availability also affect pod formation and pod thickness. Such kinds of differences in thickness of pod seems to be associated with the results as reported by Algabal (2012) [17] and Bhogave (2018) [18] in tamarind genotypes (1) The superscript letters signifies that the treatment means with similar letters are at par at 5% level of significance, while the means with different letters are significantly different at 5% level of significance. These letters have been affixed based on CD-value comparison of treatment means.
The observations regarding mature pod weight (g) of tamarind genotypes showed significant variations among the different genotypes observed under present investigation. The data observed in reference to mature pod weight has enumerated in Table 2 and graphically illustrated in Fig. 4. that the mature po During the first year of research, it was noticed that the mature pod weight of tamarind genotypes ranged from 8.99 g (STAM-26) to 33.47 g (STAM-9). As per the data obtained in Table 2, it can be concluded that various genotypes showed variation with respect to mature pod weight of tamarind. Among the various genotypes, the maximum mature pod weight (32.88 g) was measured under the genotypes STAM-9, while the minimum mature pod weight (8.65 g) was recorded by STAM-26 in pooled analysis under present investigation. Variability in the mature pod weight of tamarind genotypes may be attributed to both genetic and environmental factors. Genetic differences among genotypes play a significant role, as each possesses unique traits influencing pod development. Additionally, variations in soil type, rainfall, temperature and other microclimatic conditions across the blocks contribute to differences in nutrient uptake and pod formation. Such kinds of differences in mature pod weight appears to be associated with the results as reported by Biradar (2001) [15] , Shukla (2006) [12] and Praveenakumar et al. (2020) [13] in tamarind genotypes.
The observations regarding pulp weight per pod (g) of tamarind genotypes showed significant differences among the different genotypes observed under present investigation, which are summarized in Table 2 and graphically shown in Fig. 5. During the first year of research, it was noticed that the pulp weight per pod of tamarind genotypes ranged from 3.56 g (STAM-26) to 16.63 g (STAM-9). .28 g were found statistically at par to each other under the present investigation. Additionally, the genotypes STAM-26, STAM-35, STAM-13, STAM-2, STAM-42, STAM-25 & STAM-9 having the respective pulp weight per pod of 3.42, 4.63, 9.84, 12.28, 14.17, 15.28 & 16.86 g were found significant differences between each other under the present exploration. Whereas, the minimum pulp weight per pod (3.42 g) was registered under the genotype STAM-9. As per the data obtained in Table 2, it can be concluded that various genotypes showed variation with respect to pulp weight per pod of tamarind fruits. Among the various genotypes, the maximum pulp weight per pod (16.86 g) was measured under the genotypes STAM-9, while the minimum pulp weight per pod (3.42 g) was recorded by STAM-26 in pooled analysis under present investigation. Variations in the pulp weight per pod of tamarind genotypes are due to different genetic makeup of each genotype, this inherent genetic variation causes differences in pulp weight. Additionally, conditions like soil fertility, rainfall and temperature in different blocks of Surguja district nutrient absorption and this interaction between genetic potential and environmental conditions lead to variability in pulp weight per pod. Such kinds of differences in pulp weight also reported by Sharma et al. (2015) [19] and Mishra (2021) [14] in tamarind genotypes.
The data represent to shell weight per pod (g) of tamarind genotypes showed significant variation among each other under the present trial. The data observed in reference to shell weight per pod has been presented in the Table 2 and graphically depicted in Fig. 6. From the Table 2, it was clear that the minimum shell weight per pod (1.48 g) was registered under the genotypes STAM-1. As per the data obtained in Table 2, it can be concluded that various genotypes showed variation with respect to shell weight per pod of tamarind fruits. Among the various genotypes, the minimum shell weight per pod (1.41 g) was observed under the genotypes STAM-1, while the maximum shell weight per pod (7.11 g) was recorded by STAM-25 in pooled analysis under present investigation. Variability in the shell weight per pod of tamarind genotypes depends on the inherent genetic potential and the influence of environmental condition during pod development. Such kinds of differences in shell weight reported by Divakara et al. (2012) [20] and Raut et al. (2022) [21] in tamarind genotypes. Conti…
Conclusion
The present study reveals wide variation among pod characteristics of tamarind genotypes. Tamarind genotype STAM-9 recorded the highest mature pod weight (32.88 g), mature pod length (16.85 cm) and pulp weight per pod (16.86 g), highlighting its potential for improving overall pod yield. Similarly, STAM-40 exhibited the maximum pod width (2.84 cm), STAM-15 showed the highest pod thickness (1.8 cm), STAM-1 recorded the lowest shell weight per pod (1.41 g) and STAM-26 displayed the minimum fibre weight per pod (0.18 g). Since pod length, pod width and pulp weight were found to be closely associated with total yield, these traits hold considerable value as selection criteria in tamarind improvement programs. Genotypes exhibiting low shell and fibre content alongside high pulp weight are particularly desirable, as they directly contribute to greater processing efficiency and economic returns. Accordingly, STAM-9, STAM-40, STAM-15, STAM-1, and STAM-26 may be recommended for further exploitation, either through direct selection or as elite parents in hybridization programs targeted at developing high-yielding tamarind cultivars with superior pod quality.
References
- Mishra RN. Tamarindus indica L.: An overview of tree improvement, proceedings of National Symposium on Tamarindus indica L. 27-28 June, Tirupathi (A.P.), organized by Forest Department of Andra Pradesh. 1997:51-58.
- Morton J. Tamarind, fruit of warm climates. Creative resource system Inc. Miami, Florida, USA. 1987:115-121.
- Brandis D. Indian Trees (Tamarindus Indica Linn.). Constable and Co, Ltd. London. 1921:52-253.
- Ridley HN. The Flora of the Malay Peninsula. Tamarindus Indica Linn.: Polypetalae Reeve & Co, Ltd. London. 1922;47(1):636.
- Dalziel JM. The Useful Plants of West Tropical Africa. Crown Agents for Overseas Governments and Administrations, London. 1937:612.
- Irvine FR. Woody Plants of Ghana. Oxford University Press, London. 1961:868.
- Das DK, Alam MK. Trees of Bangladesh. Bangladesh Forest Research Institute, Chittagong, Bangladesh. 2001:224.
- George CK, Radhakrishnan VV. Tree Spices -Trees and Tree Farming, P. K. Thampan, Peckay Tree Crops Development Foundation, Cochin. 1993.
- Jayaweera DMA. Medicinal Plants (Indigenous and Exotic) Used in Ceylon. Part II. Flacourtiaceae-Lytharaceae. National Science Council of Sri Lanka, Colombo. 1981:244-246.
- Rajamanickam C. Genetic variability, Correlation and path analysis in tamarind (Tamarindus indica L.). Journal of Spices and Aromatic Crops. 2020;29(2):133-139.
- Radhamani A, Nicodemus A, Nagarajan B, Mandal AK. Reproductive biology of tropical trees. Forest genetics and tree breeding. New Delhi: CBS Publishers; 1998.
- Vishwavidyalaya, Raipur, Chhattisgarh; 2006.
- Praveenakumar R, Gopinath G, Shyamalamma S, Ramesh S, Vasundhara M, Chandre Gowda M. Studies on Phytochemical Evaluation of Tamarind (Tamarindus indica L.) Genotypes Prevailing in Eastern Dry Zone of Karnataka. Indian Journal of Pure & Applied Biosciences. 2020;8(5):320-324.
- Mishra S. Variability studies in tamarind genotypes. M.Sc. (Hort.) thesis. Vasantrao Naik Marathwada Krishi Vidyapeeth, Parbhani, Maharashtra. 2021.
- Biradar S. Evaluation of different tamarind (Tamarindus indica L.) genotypes. M.Sc. (Hort.) thesis submitted at University of Agricultural Sciences, Dharwad. 2001.
- Prabhushankar DS. Evaluation of elite clones of tamarind (Tamarindus indica L.) M.Sc. (Hort.) thesis, University of Agricultural Sciences, GKVK, Bengaluru. 2001.
- Algabal AQAY, Pappanna N, Ajay BC, Eid A. Studies on genetic parameters and interrelationship for pulp yield and its attributes in tamarind (Tamarindus indica L.). International Journal of Plant Breeding. 2012;6(1):65-69.
- Bhogave AF. Genetic variability and divergence studies in tamarind (Tamarindus indica L.). Ph.D. submitted thesis at Dr. Panjabrao Deshmukh Krishi Vidyapeeth, Akola, Maharashtra. 2018.
- Sharma DK, Aklade SA, Virdia HM. Genetic variability in tamarind (Tamarindus indica L.) from south Gujarat. Current Horticulture. 2015;3(2):43-46.
- Divakara BN, Upadhyaya HD, Fandohan B. Identification and divergence studies of genotypes of Tamarindus indica (Fabaceae) with superior pod traits. International Journal of Biological and Chemical Sciences. 2012:1-19.
- Raut UA, Jadhav SB, Mahalle SP. Character association studies in tamarind (Tamarindus indica L.) for yield and yield contributing characters. The Pharma Innovation Journal. 2022;11(11):973-982.
- Purseglove JW. A book of Tropical crops-Dicotyledon. Longman Science and Technology. 1987:204-206.
- How to cite this article: Minz V, Panigrahi HK, Singh P, Mehta N. Study of variability in pod characteristics of indigenous tamarind (Tamarindus indica L.) genotypes. International Journal of Advanced Biochemistry Research. 2026;SP10(9):2203-2211. doi: https://www.doi.org/10.33545/26174693.2 026.v10.i9Saa.10111
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