Assessment of salinity tolerance in soybean (Glycine max L.) through germination performance

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Diana Karina Ramírez Andrade
Gabriela Eugenia Ajila Celi

Abstract

Introduction. Salinity may leave the onset of germination unchanged while impairing the formation of functional seedlings, early growth, and biomass accumulation in soybeans. Objective. To evaluate the response of soybean seeds to 0, 50, and 100 mM NaCl using early germination, seedling normality, growth, and biomass indicators. Methodology. A completely randomized design was used with three treatments and six experimental units per treatment, each containing 50 seeds from a commercial lot whose varietal identity was not declared. The test was maintained for eight days at 25 ± 2 °C under a 12 h photoperiod. Germination on day 5, normal seedlings on day 8, shoot and root lengths, water loss, and dry mass were measured. Data were analyzed by one-way ANOVA and Tukey’s test at 5%. Results. Day-5 germination remained between 88.83% and 94.00%, with no statistical differences. In contrast, normal seedlings decreased from 83.33% in the control to 57.83% and 45.83% at 50 and 100 mM. At 100 mM, shoot and root lengths reached 1.85 and 3.20 cm, water loss increased to 79.34%, and root and shoot dry mass decreased to 0.06 and 0.87 g. Conclusion. The evaluated seed lot retained a high capacity to initiate germination, whereas early seedling establishment was sensitive to NaCl, especially at 100 mM. Seedling normality, growth, and biomass discriminated against stress more effectively than the first germination count. General area of study: Agricultural sciences. Specific area of study: Plant physiology and seed technology. Type of study: Original article.

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Ramírez Andrade, D. K., & Ajila Celi , G. E. (2026). Assessment of salinity tolerance in soybean (Glycine max L.) through germination performance. AlfaPublicaciones, 8(3), 70–84. https://doi.org/10.33262/ap.v8i3.705
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References

Alzahrani, Y. (2024). Evaluation of drought and salinity tolerance potentials of different soybean genotypes based upon physiological, biochemical, and genetic indicators. Frontiers in Plant Science, 15, 1466363. https://doi.org/10.3389/fpls.2024.1466363

Arciniega Alvarado, G. A., Jaramillo Jaramillo, F. L., & Muñoz García, P. L. (2018). Diseño y desarrollo de un producto funcional de consumo (pan) a base de soya, máchica, amaranto y chía. Ciencia Digital, 2(2), 391-404. https://doi.org/10.33262/cienciadigital.v2i2.103

Begum, N., Hasanuzzaman, M., Li, Y., Akhtar, K., Zhang, C., & Zhao, T. (2022). Seed germination behavior, growth, physiology and antioxidant metabolism of four contrasting cultivars under combined drought and salinity in soybean. Antioxidants, 11(3), 498. https://doi.org/10.3390/antiox11030498

Chen, L., Peng, L., Ouyang, W., Yao, H., Ye, Y., Shan, Z., Cao, D., Chen, S., Yang, Z., Huang, Y., Han, B., Sha, A., Zhou, X., & Chen, H. (2024). Screening and identification of salt tolerance soybean varieties and germplasms. Oil Crop Science, 9(3), 204-210. https://doi.org/10.1016/j.ocsci.2024.06.005

Feng, C., Gao, H., Zhou, Y., Jing, Y., Li, S., Yan, Z., Xu, K., Zhou, F., Zhang, W., Yang, X., Hussain, M. A., & Li, H. (2023). Unfolding molecular switches for salt stress resilience in soybean: recent advances and prospects for salt-tolerant smart plant production. Frontiers in Plant Science, 14, 1162014. https://doi.org/10.3389/fpls.2023.1162014

Gaibor Vallejo, L. M., Carrasco Schuldt, Ángel S., Núñez Rodríguez, P. J., Flores Cadena, C. A., Vargas Guillén, P. I., & Méndez Parra, K. M. (2024). Análisis sensorial y nutricional de un manjar elaborado con leche de vaca y bebida vegana de soya (Glycine max), quinua (Chenopodium quinoa) y lenteja (Lens culinaris). Alfa Publicaciones, 6(1.1), 112–127. https://doi.org/10.33262/ap.v6i1.1.459

Gobade, A., Arathi, S., Gijare, S., Pawar, D., & Patil, A. (2025). Evaluating salt tolerance in soybean core collection: germination response under salinity stress. Genetic Resources and Crop Evolution, 72(2), 2059–2076. https://doi.org/10.1007/s10722-024-02081-5

Guan, R.-X., Guo, X.-Y., Qu, Y., Zhang, Z.-W., Bao, L.-G., Ye, R.-Y., Chang, R.-Z., & Qiu, L.-J. (2024). Salt tolerance in soybeans: focus on screening methods and genetics. Plants, 13(1), 97. https://doi.org/10.3390/plants13010097

Han, L., Ge, L., Fei, L., Huang, C., Li, Y., Fan, W., Zhu, D., & Zhao, L. (2025). A comprehensive evaluation of soybean germplasm resources for salt tolerance during germination. Plants, 14(5), 791. https://doi.org/10.3390/plants14050791

International Seed Testing Association (ISTA). (2026). International rules for seed testing. https://www.seedtest.org/en/publications/international-rules-seed-testing.html

Isayenkov, S. V., & Maathuis, F. J. (2019). Plant salinity stress: many unanswered questions remain. Frontiers in Plant Science, 10, 80. https://doi.org/10.3389/fpls.2019.00080

Kokebie, D., Enyew, A., Masresha, G., Fentie, T., & Mulat, E. (2024). Morphological, physiological, and biochemical responses of three different soybean (Glycine max L.) varieties under salinity stress conditions. Frontiers in Plant Science, 15, 1440445. https://doi.org/10.3389/fpls.2024.1440445

Liu, L., Wang, J., Zhang, Q., Sun, T., & Wang, P. (2023). Cloning of the soybean GmNHL1 gene and functional analysis under salt stress. Plants, 12(22), 3869. https://doi.org/10.3390/plants12223869

Oñate Mancero, F. J., Bravo Calle, O., Vaca Zambrano, E., & Toapanta Santacruz, S. (2019). Semillas de siratro (Macroptilium atropurpureum) sometidas a escarificación química y térmica. Ciencia Digital, 3(3.1), 167-175. https://doi.org/10.33262/cienciadigital.v3i3.1.683

Van Zelm, E., Zhang, Y., & Testerink, C. (2020). Salt tolerance mechanisms of plants. Annual review of plant biology, 71, 403–433. https://doi.org/10.1146/annurev-arplant-050718-100005

Wang, J., Zhou, M., Zhang, H., Liu, X., Zhang, W., Wang, Q., Jia, Q., Xu, D., Chen, H., & Su, C. (2024). A genome-wide association analysis for salt tolerance during the soybean germination stage and development of KASP markers. Frontiers in Plant Science, 15, 1352465. https://doi.org/10.3389/fpls.2024.1352465

Xu, R., Yang, Q., Liu, Z., Shi, X., Wu, X., Chen, Y., Du, X., Gao, Q., He, D., Shi, A., Tao, P., & Yan, L. (2024). Genome-wide association analysis and genomic prediction of salt tolerance trait in soybean germplasm. Frontiers in Plant Science, 15, 1494551. https://doi.org/10.3389/fpls.2024.1494551

Zhou, X., Tian, Y., Qu, Z., Wang, J., Han, D., & Dong, S. (2023). Comparing the salt tolerance of different spring soybean varieties at the germination stage. Plants, 12(15), 2789. https://doi.org/10.3390/plants12152789