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Yoncada (Medicago sativa L.) Tuzluluk Toleransı Farklı İki Çeşitte Fizyolojik ve Biyokimyasal Mekanizmalar

Year 2026, Volume: 23 Issue: 2, 534 - 544, 16.03.2026
https://doi.org/10.33462/jotaf.1644259
https://izlik.org/JA68DK49RD

Abstract

Tuz stresi, tarımsal verimliliği azaltan abiyotik bir stres faktörü olarak kabul edilmektedir. Yapılan araştırmalar, tuz stresinin bitkilerde büyüme, gelişme ve verim üzerinde olumsuz etkiler yarattığını, aynı zamanda kalite kayıplarına yol açtığını ortaya koymaktadır. Özellikle yem bitkileri arasında yüksek besin değerine sahip olan yaygın yonca, tuz stresine karşı hassasiyet gösteren türlerden biridir. Bu nedenle, yaygın yoncanın tuz stresine karşı fizyolojik ve biyokimyasal tepkilerini anlamak, stres toleransını artırmak için gerekli olan programların ortaya konması adına büyük önem taşımaktadır. Bu çalışmada, tuz stresine farklı duyarlılık gösteren yaygın yonca çeşitlerinin tuz stresine maruz kaldığında gösterdiği fizyolojik ve biyokimyasal mekanizmaların ortaya konulması amaçlanmıştır. Araştırma öncesinde yapılan petri deneyleri, her iki çeşidin tuz stresine karşı farklı hassasiyet gösterdiğini ve 'Diane' çeşidinin 'Bilensoy-80' çeşidine kıyasla daha dayanıklı olduğunu ortaya koymuştur. Çalışmada, farklı tuzluluk seviyelerinin (0, 50, 100, 150, 200 mM NaCl) yaygın yonca çeşitlerinde büyüme parametreleri, fizyolojik ve biyokimyasal mekanizmaya etkileri analiz edilmiştir. Çalışma sonuçları 'Diane' çeşidinin tuz stresi altında 150 ve 200 mM NaCl uygulamaları dışında kontrol grubuna kıyasla kök gelişimini, fizyolojik ve biyokimyasal durumunu koruduğunu göstermiştir. Buna karşılık, 'Bilensoy-80' çeşidinde tuz stresi kontrol grubuna kıyasla, büyüme parametrelerinde belirgin bir azalmaya, fizyolojik ve biyokimyasal özelliklerde ise ciddi bozulmalara yol açmıştır. Elde edilen sonuçlar, 'Diane' çeşidinin yüksek tuz toleransının, serbest prolin ve toplam fenolik içeriğindeki artışın yanı sıra APX, CAT ve GR enzimlerinin artan biyosentezini içeren antioksidatif savunma mekanizmasına bağlı olabileceğini göstermektedir. Araştırma bulguları, tuz stresine dayanıklı yaygın yonca bitkisi geliştirmeyi hedefleyen ıslah programlarında kullanılabilir. Ayrıca, tuz stresine daha toleranslı olduğu belirlenen 'Diane' çeşidinin, tuzlu koşullarda verim ve adaptasyon kapasitesinin değerlendirilmesi amacıyla tarla denemeleriyle test edilmesi önerilmektedir.

Ethical Statement

There is no need to obtain permission from the ethics committee for this study.

Thanks

No financial support has been received for this research.

References

  • Akhtar, S. S., Andersen, M. N. and Liu, F. (2015). Biochar mitigates salinity stress in potato. Journal of Agronomy and Crop Science, 201: 368-378.
  • Ali, S., Charles, T. C. and Glick, B. R. (2014). Amelioration of high salinity stress damage by plant growth-promoting bacterial endophytes that contain ACC deaminase. Plant Physiology and Biochemistry, 80: 160-167.
  • Ashraf, M. and Harris P. J. C. (2004). Potential use of glycine betaine in improving plant salt tolerance. Biotechnology Advances, 22(1): 33-53.
  • Babakhani, B., Khavari-Nejad, R. A., Fahimi, H. and Saadatmand, S. (2011). Biochemical responses of alfalfa (Medicago sativa L.) cultivars subjected to NaCl salinity stress. African Journal of Biotechnology, 10: 11433-11441.
  • Bates, L. S., Waldren, R. P. and Teare, I. (1973). Rapid determination of free proline for water-stress studies. Plant and Soil, 39: 205-207.
  • Beauchamp, C. and Fridovich, I. (1971). Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Analytical Biochemistry, 44: 276-287.
  • Begum, N., Hasanuzzaman, M., Li, Y., Akhtar, K., Zhang, C. and 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): 1-23.
  • Beyaz, R. and Kazankaya, A. (2024). Effect of NaCl-induced salt stress on germination and initial seedling growth of Lotus corniculatus L. cv.'Leo'. Journal of Tekirdag Agricultural Faculty, 21(1): 24-34.
  • Bicakci, T., Aksu, E. and Arslan, M. (2020). Determination of germination characteristics of covered alfalfa (Medicago sativa L.) seeds in drought stress conditions. Journal of Tekirdag Agricultural Faculty, 17(2): 124-136.
  • Bradford, M. M. (1976). A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Analytical Biochemistry, 72: 248-254.
  • Chance, B. and Maehly, A. (1955). Assay of catalases and peroxidases. Methods in Enzymology, 2: 764-775.
  • Cornacchione, M. V. and Suarez, D. L. (2017). Evaluation of alfalfa (Medicago sativa L.) populations’ response to salinity stress. Crop Science, 57: 137-150.
  • Demirci-Cekic, S., Özkan, G., Avan, A. N., Uzunboy, S, Çapanoğlu, E. and Apak, R. (2022). Biomarkers of oxidative stress and antioxidant defense. Journal of Pharmaceutical and Biomedical Analysis, 209: 1-26.
  • Demirkol, G. (2021). PopW enhances drought stress tolerance of alfalfa via activating antioxidative enzymes, endogenous hormones, drought related genes and inhibiting senescence genes. Plant Physiology and Biochemistry, 166: 540-548.
  • Demirkol, G. and Yılmaz, N. (2023). Morphologically and genetically diverse forage pea (Pisum sativum var. arvense L.) genotypes under single and combined salt and drought stresses. Plant Physiology and Biochemistry, 196: 880-892.
  • Duan, S., Zhao, L., Chen, W., Zhang, Q., Ya, J., Zhong, W. and Zhang, J. (2025). Sowing methods and strigolactones alleviate damage to the photosynthetic system of rice seedlings under salt stress by enhancing antioxidant capacity. Antioxidants, 14: 1020.
  • Farrant, J. M. (2000). A comparison of mechanisms of desiccation tolerance among three angiosperm resurrection plant species. Plant Ecology, 151: 29-39.
  • Ghaffari, H., Tadayon, M. R, Nadeem, M., Cheema, M. and Razmjoo, J. (2019). Proline-mediated changes in antioxidant enzymatic activities and the physiology of sugar beet under drought stress. Acta Physiologiae Plantarum, 41: 1-13.
  • Hasanuzzaman, M., Bhuyan, M. B., Zulfiqar, F., Raza, A., Mohsin, S. M., Mahmud, J. A., Fujita, M. and Fotopoulos, V. (2020). Reactive oxygen species and antioxidant defense in plants under abiotic stress: Revisiting the crucial role of a universal defense regulator. Antioxidants, 9(8): 1-52.
  • Jeddi, K., Siddique, K. H. M. and Hessini, K. (2025). Impact of salinity on plant growth, photosynthesis, cell wall elasticity and osmotic adjustment in damask rose. Russian Journal of Plant Physiology, 72: 171.
  • Lei, Y., Xu, Y., Hettenhausen, C., Lu, C., Shen, G., Zhang, C., Li, J., Song, J., Lin, H. and Wu, J. (2018). Comparative analysis of alfalfa (Medicago sativa L.) leaf transcriptomes reveals genotype-specific salt tolerance mechanisms. BMC Plant Biology, 18: 1-14.
  • Lundell, S. and Biligetu, B. (2024). Differential gene expression of salt-tolerant alfalfa in response to salinity and inoculation by Ensifer meliloti. BMC Plant Biology, 24: 633.
  • Maryum, Z., Luqman, T., Nadeem, S., Khan, S. M. U. D., Wang, B., Ditta, A. and Khan, M. K. R. (2022). An overview of salinity stress, mechanism of salinity tolerance and strategies for its management in cotton. Frontiers in Plant Science, 13: 907937.
  • Mueller, S. C. and Teuber, L. R. (2008). Alfalfa Growth and Development. In: Irrigated Alfalfa Management for Mediterranean and Desert Zones. Ed(s): Summers, C. G. and Putnam, D. H., ANR-UC, Oakland, Canada.
  • Mukhopadhyay, R., Sarkar, B., Jat, H. S., Sharma, P. C., Bolan, N. S. (2021). Soil salinity under climate change: Challenges for sustainable agriculture and food security. Journal of Environmental Management, 280: 111736.
  • Munns, R. and Tester, M. (2008). Mechanisms of salinity tolerance. Annual Review of Plant Biology, 59: 651-681.
  • Mushtaq, Z., Faizan, S. and Gulzar, B. (2020). Salt stress, its impacts on plants and the strategies plants are employing against it: A review. Journal of Applied Biology and Biotechnology, 8: 81-91.
  • Ohkawa, H., Ohishi, N. and Yagi, K. (1979). Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry, 95: 351-358.
  • Ondrasek, G., Rathod, S., Manohara, K. K., Gireesh, C., Anantha, M. S., Sakhare, A.S., Parmar, B., Yadav, B. K., Bandumula, N. and Raihan, F. (2022). Salt stress in plants and mitigation approaches. Plants, 11: 1-21.
  • Porra, R. J., Thompson, W. A. and Kriedemann, P. E. (1989). Determination of accurate extinction coefficients and simultaneous equations for assaying chlorophylls a and b extracted with four different solvents: verification of the concentration of chlorophyll standards by atomic absorption spectroscopy. Biochimica et Biophysica Acta (BBA)-Bioenergetics, 975: 384-394.
  • Pour-Aboughadareh, A., Ahmadi, J., Mehrabi, A. A., Etminan, A., Moghaddam, M. and Siddique, K. H. (2017). Physiological responses to drought stress in wild relatives of wheat: implications for wheat improvement. Acta Physiologiae Plantarum, 39: 106.
  • Rajasheker, G., Jawahar, G., Jalaja, N., Kumar, S. A., Kumari, P. H., Punita, D. L., Karumanchi, A. R., Reddy, P. S., Rathnagiri, P. and Sreenivasulu, N. (2019). Role and Regulation of Osmolytes and ABA Interaction in Salt and Drought Stress Tolerance. In: Plant Signaling Molecules. Ed(s): Khan, M. I. R., Reddy, P. S., Ferrante, A. and Khan, N. A., Elsevier, Amsterdam, Holland.
  • Rao, M. J., Duan, M., Zhou, C., Jiao, J., Cheng, P., Yang, L. and Zheng, B. (2025). Antioxidant defense system in plants: Reactive oxygen species production, signaling, and scavenging during abiotic stress-induced oxidative damage. Horticulturae, 11: 1-33.
  • Riseh, R. S., Fathi, F., Vatankhah, M. and Kennedy, J. F. (2024). Catalase-associated immune responses in plant-microbe interactions: A review. International Journal of Biological Macromolecules, 135859.
  • Sgherri, C. L. M., Loggini, B., Puliga, S. and Navari-Izzo, F. (1994). Antioxidant system in Sporobolus stapfianus: changes in response to desiccation and rehydration. Phytochemistry, 35: 561-565.
  • Sharavdorj, K., Jang, Y., Byambadorj, S. O. and Cho, J. W. (2021). Understanding seed germination of forage crops under various salinity and temperature stress. Journal of Crop Science and Biotechnology, 24: 545-554.
  • Slinkard, K. and Singleton, V. L. (1977). Total phenol analysis: automation and comparison with manual methods. American Journal of Enology and Viticulture, 28: 49-55.
  • Waadt, R., Seller, C. A., Hsu, P. K., Takahashi, Y., Munemasa, S. and Schroeder, J. I. (2022). Plant hormone regulation of abiotic stress responses. Nature Reviews Molecular Cell Biology, 23(10): 680-694.
  • Wang, S. Y., Jiao, H. J. and Faust, M. (1991). Changes in ascorbate, glutathione, and related enzyme activities during thidiazuron‐induced bud break of apple. Physiologia Plantarum, 82: 231-236.
  • Yılmaz, V. A. (2019). Investigation of bioactive compounds and antioxidant capacities of various cereal products. Journal of Agricultural Faculty of Gaziosmanpaşa University, 36: 10-22.
  • Zou, Y., Zhang, Y. and Testerink C. (2022). Root dynamic growth strategies in response to salinity. Plant, Cell & Environment, 45: 695-704.
  • Zrig, A, Tounekti, T., Hegab, M. M., Ali, S. O. and Khemira, H. (2016). Essential oils, amino acids and polyphenols changes in salt-stressed Thymus vulgaris exposed to open–field and shade enclosure. Industrial Crops and Products, 91: 223-230.

Physiological and Biochemical Mechanisms in Two Alfalfa (Medicago sativa L.) Cultivars with Contrasting Salinity Tolerance

Year 2026, Volume: 23 Issue: 2, 534 - 544, 16.03.2026
https://doi.org/10.33462/jotaf.1644259
https://izlik.org/JA68DK49RD

Abstract

Salinity stress has been accepted as an abiotic stress factor that decreases agricultural productivity. Earlier studies have showed that salinity stress has a negative impact on plant growth, development, and yield, while also leading to quality losses. Among forage crops, alfalfa is one of the species that exhibits sensitivity to salinity stress. Thus, gaining insights into the physiological and biochemical mechanisms of alfalfa under salinity stress is essential for formulating effective strategies to improve its tolerance. This study aimed to reveal the physiological and biochemical mechanisms of two alfalfa cultivars showing different sensitivity to salinity stress when exposed to salt stress. Preliminary petri dish experiments conducted before the study revealed that the two alfalfa cultivars exhibited different sensitivities to salinity stress, with the 'Diane' being more tolerant compared to 'Bilensoy-80'. In the study, the effects of varying salinity levels (0, 50, 100, 150, 200 mM NaCl) were tested in alfalfa cultivars by performing growth parameters, physiological and biochemical status. The results indicated that the cultivar 'Diane' showed maintained root development, physiological and biochemical status, compared to control under salinity stress, except for 150 and 200 mM NaCl. In contrast, salinity stress in the 'Bilensoy-80' caused a significant reduction in growth parameters and severe impairments in physiological and biochemical traits, compared to control. The results collectively revealed that higher salinity tolerance in 'Diane' could be attributed to its increased free proline content and antioxidative defense mechanism, including total phenolic content, APX, CAT and GR enzyme biosynthesis. The findings of this study can be used in breeding strategies that aimed to develop salt-tolerant alfalfa plants. Additionally, it is recommended that the 'Diane' cultivar, which has been identified as more tolerant to salinity stress, be tested through field trials to evaluate its yield and adaptation capacity under saline conditions.

Ethical Statement

There is no need to obtain permission from the ethics committee for this study.

Thanks

No financial support has been received for this research.

References

  • Akhtar, S. S., Andersen, M. N. and Liu, F. (2015). Biochar mitigates salinity stress in potato. Journal of Agronomy and Crop Science, 201: 368-378.
  • Ali, S., Charles, T. C. and Glick, B. R. (2014). Amelioration of high salinity stress damage by plant growth-promoting bacterial endophytes that contain ACC deaminase. Plant Physiology and Biochemistry, 80: 160-167.
  • Ashraf, M. and Harris P. J. C. (2004). Potential use of glycine betaine in improving plant salt tolerance. Biotechnology Advances, 22(1): 33-53.
  • Babakhani, B., Khavari-Nejad, R. A., Fahimi, H. and Saadatmand, S. (2011). Biochemical responses of alfalfa (Medicago sativa L.) cultivars subjected to NaCl salinity stress. African Journal of Biotechnology, 10: 11433-11441.
  • Bates, L. S., Waldren, R. P. and Teare, I. (1973). Rapid determination of free proline for water-stress studies. Plant and Soil, 39: 205-207.
  • Beauchamp, C. and Fridovich, I. (1971). Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Analytical Biochemistry, 44: 276-287.
  • Begum, N., Hasanuzzaman, M., Li, Y., Akhtar, K., Zhang, C. and 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): 1-23.
  • Beyaz, R. and Kazankaya, A. (2024). Effect of NaCl-induced salt stress on germination and initial seedling growth of Lotus corniculatus L. cv.'Leo'. Journal of Tekirdag Agricultural Faculty, 21(1): 24-34.
  • Bicakci, T., Aksu, E. and Arslan, M. (2020). Determination of germination characteristics of covered alfalfa (Medicago sativa L.) seeds in drought stress conditions. Journal of Tekirdag Agricultural Faculty, 17(2): 124-136.
  • Bradford, M. M. (1976). A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Analytical Biochemistry, 72: 248-254.
  • Chance, B. and Maehly, A. (1955). Assay of catalases and peroxidases. Methods in Enzymology, 2: 764-775.
  • Cornacchione, M. V. and Suarez, D. L. (2017). Evaluation of alfalfa (Medicago sativa L.) populations’ response to salinity stress. Crop Science, 57: 137-150.
  • Demirci-Cekic, S., Özkan, G., Avan, A. N., Uzunboy, S, Çapanoğlu, E. and Apak, R. (2022). Biomarkers of oxidative stress and antioxidant defense. Journal of Pharmaceutical and Biomedical Analysis, 209: 1-26.
  • Demirkol, G. (2021). PopW enhances drought stress tolerance of alfalfa via activating antioxidative enzymes, endogenous hormones, drought related genes and inhibiting senescence genes. Plant Physiology and Biochemistry, 166: 540-548.
  • Demirkol, G. and Yılmaz, N. (2023). Morphologically and genetically diverse forage pea (Pisum sativum var. arvense L.) genotypes under single and combined salt and drought stresses. Plant Physiology and Biochemistry, 196: 880-892.
  • Duan, S., Zhao, L., Chen, W., Zhang, Q., Ya, J., Zhong, W. and Zhang, J. (2025). Sowing methods and strigolactones alleviate damage to the photosynthetic system of rice seedlings under salt stress by enhancing antioxidant capacity. Antioxidants, 14: 1020.
  • Farrant, J. M. (2000). A comparison of mechanisms of desiccation tolerance among three angiosperm resurrection plant species. Plant Ecology, 151: 29-39.
  • Ghaffari, H., Tadayon, M. R, Nadeem, M., Cheema, M. and Razmjoo, J. (2019). Proline-mediated changes in antioxidant enzymatic activities and the physiology of sugar beet under drought stress. Acta Physiologiae Plantarum, 41: 1-13.
  • Hasanuzzaman, M., Bhuyan, M. B., Zulfiqar, F., Raza, A., Mohsin, S. M., Mahmud, J. A., Fujita, M. and Fotopoulos, V. (2020). Reactive oxygen species and antioxidant defense in plants under abiotic stress: Revisiting the crucial role of a universal defense regulator. Antioxidants, 9(8): 1-52.
  • Jeddi, K., Siddique, K. H. M. and Hessini, K. (2025). Impact of salinity on plant growth, photosynthesis, cell wall elasticity and osmotic adjustment in damask rose. Russian Journal of Plant Physiology, 72: 171.
  • Lei, Y., Xu, Y., Hettenhausen, C., Lu, C., Shen, G., Zhang, C., Li, J., Song, J., Lin, H. and Wu, J. (2018). Comparative analysis of alfalfa (Medicago sativa L.) leaf transcriptomes reveals genotype-specific salt tolerance mechanisms. BMC Plant Biology, 18: 1-14.
  • Lundell, S. and Biligetu, B. (2024). Differential gene expression of salt-tolerant alfalfa in response to salinity and inoculation by Ensifer meliloti. BMC Plant Biology, 24: 633.
  • Maryum, Z., Luqman, T., Nadeem, S., Khan, S. M. U. D., Wang, B., Ditta, A. and Khan, M. K. R. (2022). An overview of salinity stress, mechanism of salinity tolerance and strategies for its management in cotton. Frontiers in Plant Science, 13: 907937.
  • Mueller, S. C. and Teuber, L. R. (2008). Alfalfa Growth and Development. In: Irrigated Alfalfa Management for Mediterranean and Desert Zones. Ed(s): Summers, C. G. and Putnam, D. H., ANR-UC, Oakland, Canada.
  • Mukhopadhyay, R., Sarkar, B., Jat, H. S., Sharma, P. C., Bolan, N. S. (2021). Soil salinity under climate change: Challenges for sustainable agriculture and food security. Journal of Environmental Management, 280: 111736.
  • Munns, R. and Tester, M. (2008). Mechanisms of salinity tolerance. Annual Review of Plant Biology, 59: 651-681.
  • Mushtaq, Z., Faizan, S. and Gulzar, B. (2020). Salt stress, its impacts on plants and the strategies plants are employing against it: A review. Journal of Applied Biology and Biotechnology, 8: 81-91.
  • Ohkawa, H., Ohishi, N. and Yagi, K. (1979). Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry, 95: 351-358.
  • Ondrasek, G., Rathod, S., Manohara, K. K., Gireesh, C., Anantha, M. S., Sakhare, A.S., Parmar, B., Yadav, B. K., Bandumula, N. and Raihan, F. (2022). Salt stress in plants and mitigation approaches. Plants, 11: 1-21.
  • Porra, R. J., Thompson, W. A. and Kriedemann, P. E. (1989). Determination of accurate extinction coefficients and simultaneous equations for assaying chlorophylls a and b extracted with four different solvents: verification of the concentration of chlorophyll standards by atomic absorption spectroscopy. Biochimica et Biophysica Acta (BBA)-Bioenergetics, 975: 384-394.
  • Pour-Aboughadareh, A., Ahmadi, J., Mehrabi, A. A., Etminan, A., Moghaddam, M. and Siddique, K. H. (2017). Physiological responses to drought stress in wild relatives of wheat: implications for wheat improvement. Acta Physiologiae Plantarum, 39: 106.
  • Rajasheker, G., Jawahar, G., Jalaja, N., Kumar, S. A., Kumari, P. H., Punita, D. L., Karumanchi, A. R., Reddy, P. S., Rathnagiri, P. and Sreenivasulu, N. (2019). Role and Regulation of Osmolytes and ABA Interaction in Salt and Drought Stress Tolerance. In: Plant Signaling Molecules. Ed(s): Khan, M. I. R., Reddy, P. S., Ferrante, A. and Khan, N. A., Elsevier, Amsterdam, Holland.
  • Rao, M. J., Duan, M., Zhou, C., Jiao, J., Cheng, P., Yang, L. and Zheng, B. (2025). Antioxidant defense system in plants: Reactive oxygen species production, signaling, and scavenging during abiotic stress-induced oxidative damage. Horticulturae, 11: 1-33.
  • Riseh, R. S., Fathi, F., Vatankhah, M. and Kennedy, J. F. (2024). Catalase-associated immune responses in plant-microbe interactions: A review. International Journal of Biological Macromolecules, 135859.
  • Sgherri, C. L. M., Loggini, B., Puliga, S. and Navari-Izzo, F. (1994). Antioxidant system in Sporobolus stapfianus: changes in response to desiccation and rehydration. Phytochemistry, 35: 561-565.
  • Sharavdorj, K., Jang, Y., Byambadorj, S. O. and Cho, J. W. (2021). Understanding seed germination of forage crops under various salinity and temperature stress. Journal of Crop Science and Biotechnology, 24: 545-554.
  • Slinkard, K. and Singleton, V. L. (1977). Total phenol analysis: automation and comparison with manual methods. American Journal of Enology and Viticulture, 28: 49-55.
  • Waadt, R., Seller, C. A., Hsu, P. K., Takahashi, Y., Munemasa, S. and Schroeder, J. I. (2022). Plant hormone regulation of abiotic stress responses. Nature Reviews Molecular Cell Biology, 23(10): 680-694.
  • Wang, S. Y., Jiao, H. J. and Faust, M. (1991). Changes in ascorbate, glutathione, and related enzyme activities during thidiazuron‐induced bud break of apple. Physiologia Plantarum, 82: 231-236.
  • Yılmaz, V. A. (2019). Investigation of bioactive compounds and antioxidant capacities of various cereal products. Journal of Agricultural Faculty of Gaziosmanpaşa University, 36: 10-22.
  • Zou, Y., Zhang, Y. and Testerink C. (2022). Root dynamic growth strategies in response to salinity. Plant, Cell & Environment, 45: 695-704.
  • Zrig, A, Tounekti, T., Hegab, M. M., Ali, S. O. and Khemira, H. (2016). Essential oils, amino acids and polyphenols changes in salt-stressed Thymus vulgaris exposed to open–field and shade enclosure. Industrial Crops and Products, 91: 223-230.
There are 42 citations in total.

Details

Primary Language English
Subjects Pasture-Meadow Forage Plants, Crop and Pasture Biochemistry and Physiology
Journal Section Research Article
Authors

Gürkan Demirkol 0000-0003-0033-8039

Submission Date February 21, 2025
Acceptance Date January 25, 2026
Publication Date March 16, 2026
DOI https://doi.org/10.33462/jotaf.1644259
IZ https://izlik.org/JA68DK49RD
Published in Issue Year 2026 Volume: 23 Issue: 2

Cite

APA Demirkol, G. (2026). Physiological and Biochemical Mechanisms in Two Alfalfa (Medicago sativa L.) Cultivars with Contrasting Salinity Tolerance. Tekirdağ Ziraat Fakültesi Dergisi, 23(2), 534-544. https://doi.org/10.33462/jotaf.1644259
AMA 1.Demirkol G. Physiological and Biochemical Mechanisms in Two Alfalfa (Medicago sativa L.) Cultivars with Contrasting Salinity Tolerance. Tekirdağ Ziraat Fakültesi Dergisi. 2026;23(2):534-544. doi:10.33462/jotaf.1644259
Chicago Demirkol, Gürkan. 2026. “Physiological and Biochemical Mechanisms in Two Alfalfa (Medicago Sativa L.) Cultivars With Contrasting Salinity Tolerance”. Tekirdağ Ziraat Fakültesi Dergisi 23 (2): 534-44. https://doi.org/10.33462/jotaf.1644259.
EndNote Demirkol G (March 1, 2026) Physiological and Biochemical Mechanisms in Two Alfalfa (Medicago sativa L.) Cultivars with Contrasting Salinity Tolerance. Tekirdağ Ziraat Fakültesi Dergisi 23 2 534–544.
IEEE [1]G. Demirkol, “Physiological and Biochemical Mechanisms in Two Alfalfa (Medicago sativa L.) Cultivars with Contrasting Salinity Tolerance”, Tekirdağ Ziraat Fakültesi Dergisi, vol. 23, no. 2, pp. 534–544, Mar. 2026, doi: 10.33462/jotaf.1644259.
ISNAD Demirkol, Gürkan. “Physiological and Biochemical Mechanisms in Two Alfalfa (Medicago Sativa L.) Cultivars With Contrasting Salinity Tolerance”. Tekirdağ Ziraat Fakültesi Dergisi 23/2 (March 1, 2026): 534-544. https://doi.org/10.33462/jotaf.1644259.
JAMA 1.Demirkol G. Physiological and Biochemical Mechanisms in Two Alfalfa (Medicago sativa L.) Cultivars with Contrasting Salinity Tolerance. Tekirdağ Ziraat Fakültesi Dergisi. 2026;23:534–544.
MLA Demirkol, Gürkan. “Physiological and Biochemical Mechanisms in Two Alfalfa (Medicago Sativa L.) Cultivars With Contrasting Salinity Tolerance”. Tekirdağ Ziraat Fakültesi Dergisi, vol. 23, no. 2, Mar. 2026, pp. 534-4, doi:10.33462/jotaf.1644259.
Vancouver 1.Gürkan Demirkol. Physiological and Biochemical Mechanisms in Two Alfalfa (Medicago sativa L.) Cultivars with Contrasting Salinity Tolerance. Tekirdağ Ziraat Fakültesi Dergisi. 2026 Mar. 1;23(2):534-4. doi:10.33462/jotaf.1644259