Synergistic Biochar and Mycorrhizal Fungi Application Alleviates Cadmium Toxicity and Salinity Stress by Enhancing Soil Functioning and Tomato Productivity
DOI:
https://doi.org/10.56946/jspae.v5i2.956Keywords:
Biochar, Mycorrhizea, Cd toxicity, Salinity, Cd StressAbstract
Tomato production is increasingly constrained by cadmium (Cd) contamination and abiotic stresses, which impair plant growth, fruit quality, and food safety. Innovative and eco-friendly strategies are therefore needed to mitigate these constraints. Biochar and mycorrhizal fungi, applied individually or synergistically, have the potential to improve soil biochemical properties, reduce metal bioavailability and toxicity, and enhance tomato growth and fruit quality under stress conditions. This study evaluated the synergistic effects of biochar (0, 1%, and 2% w/w) and mycorrhizal fungi on soil biochemical functioning, Cd bioavailability, and tomato growth in saline soil. The combined application of mycorrhizal fungi and biochar at 2% (w/w) significantly increased soil respiration and phosphatase, nitrogenase, and dehydrogenase activities by 140%, 127%, 330%, and 130%, respectively, while reducing soil electrical conductivity and available Cd concentrations by 29.9% and 59%, respectively. This treatment also markedly decreased Cd accumulation in tomato shoots, roots, and fruits by 37%, 40%, and 93%, respectively, accompanied by reductions of 6% and 56% in the translocation factor and biological concentration factor, respectively. Furthermore, electrolyte leakage and the contents of proline, malondialdehyde, and hydrogen peroxide decreased by 77%, 50%, 94%, and 79.9%, respectively, whereas the activities of antioxidant enzymes, including polyphenol oxidase, peroxidase, catalase, and superoxide dismutase, increased by 129%, 80%, 81%, and 59%, respectively. These improvements in soil biochemical properties and plant physiological responses were associated with an 80.8% increase in tomato yield. Overall, the synergistic application of biochar and mycorrhizal fungi effectively alleviated Cd toxicity, improved soil biochemical functioning, enhanced antioxidant defense, and promoted tomato growth and productivity under saline stress.
References
1. Ma, J., Saleem, M. H., Ali, B., Rasheed, R., Ashraf, M. A., Aziz, H., & Marc, R. A. (2022). Impact of foliar application of syringic acid on tomato (Solanum lycopersicum L.) under heavy metal stress-insights into nutrient uptake, redox homeostasis, oxidative stress, and antioxidant defense. Frontiers in Plant Science, 13, 950120. https://doi.org/10.3389/fpls.2022.950120
2. Roșca, M., Mihalache, G., & Stoleru, V. (2023). Tomato responses to salinity stress: From morphological traits to genetic changes. Frontiers in plant science, 14, 1118383 https://doi.org/10.3389/fpls.2023.1118383
3. Vasilachi, I. C., Stoleru, V., & Gavrilescu, M. (2023). Analysis of heavy metal impacts on cereal crop growth and development in contaminated soils. Agriculture, 13(10), 1983. https://doi.org/10.3390/agriculture13101983
4. Ali, I., Ali, A., Manan, F., Ullah, S., & Xu, X. (2026). Carbon-rich biochar as a sustainable remediator of antimony contamination: a critical review. Journal of Soil Science and Plant Nutrition, 26(1), 2277-2294 https://doi.org/10.1007/s42729-025-02996-7
5. Li, Q., & Imran. (2025). Using biochar, compost, and dry-based organic amendments in combination with mycorrhizae for mitigating heavy metal contamination in soil. International Journal of Phytoremediation, 27(10), 1502-1513. https://doi.org/10.1080/15226514.2025.2502458
6. Briffa, J.; Sinagra, E.; Blundell, R. Heavy metal pollution in the environment and their toxicological effects on humans. Heliyon 2020, 6, 26. https://doi.org/10.1016/j.heliyon.2020.e04691
7. Hou, D., O'Connor, D., Igalavithana, A. D., Alessi, D. S., Luo, J., Tsang, D. C., & Ok, Y. S. (2020). Metal contamination and bioremediation of agricultural soils for food safety and sustainability. Nature Reviews Earth & Environment, 1(7), 366-381. https://doi.org/10.1038/s43017-020-0061-y
8. Ankush, Ritambhara, Lamba, S., Deepika, & Prakash, R. (2024). Cadmium in environment-an overview. Cadmium Toxicity in Water: Challenges and Solutions, 3-20. https://doi.org/10.1007/978-3-031-54005-9_1
9. Khan, A., Khan, S., Khan, M. A., Qamar, Z., & Waqas, M. (2015). The uptake and bioaccumulation of heavy metals by food plants, their effects on plants nutrients, and associated health risk: a review. Environmental science and pollution research, 22(18), 13772-13799. https://doi.org/10.1007/s11356-015-4881-0
10. Jian, L., Jingchun, L., Chongling, Y., Daolin, D., & Haoliang, L. (2019). The alleviation effect of iron on cadmium phytotoxicity in mangrove A. marina. Alleviation effect of iron on cadmium phytotoxicity in mangrove Avicennia marina (Forsk.) Vierh. Chemosphere, 226, 413-420. https://doi.org/10.1016/j.chemosphere.2019.03.172
11.Töpperwien, S., Behra, R., & Sigg, L. (2007). Competition among zinc, manganese, and cadmium uptake in the freshwater alga Scenedesmus vacuolatus. Environmental toxicology and chemistry, 26(3), 483-490. https://doi.org/10.1897/06-181R.1
12. Sachdev, S., Ansari, S. A., Ansari, M. I., Fujita, M., & Hasanuzzaman, M. (2021). Abiotic stress and reactive oxygen species: Generation, signaling, and defense mechanisms. Antioxidants, 10(2), 277. https://doi.org/10.3390/antiox10020277
13. Singh, A. (2022). Soil salinity: A global threat to sustainable development. Soil Use and Management, 38(1), 39-67. https://doi.org/10.1111/sum.12772
14. El Sabagh, A., Islam, M. S., Skalicky, M., Ali Raza, M., Singh, K., Anwar Hossain, M., & Arshad, A. (2021). Salinity stress in wheat (Triticum aestivum L.) in the changing climate: Adaptation and management strategies. Frontiers in Agronomy, 3, 661932. https://doi.org/10.3389/fagro.2021.661932
15. Ahmad, R., Hussain, S., Anjum, M. A., Khalid, M. F., Saqib, M., Zakir, I., & Ahmad, S. (2019). Oxidative stress and antioxidant defense mechanisms in plants under salt stress. In Plant abiotic stress tolerance: Agronomic, molecular and biotechnological approaches (pp. 191-205). Cham: Springer International Publishing. https://doi.org/10.1007/978-3-030-06118-0_8
16. Liang, L., Liu, W., Sun, Y., Huo, X., Li, S., & Zhou, Q. (2017). Phytoremediation of heavy metal contaminated saline soils using halophytes: current progress and future perspectives. Environmental Reviews, 25(3), 269-281. https://doi.org/10.1139/er-2016-0063
17. Bajon, A., Kidoń, M., & Kobus-Cisowska, J. (2026). Tomato (Solanum lycopersicum L.) as a Source of Bioactive Compounds: Functional Properties and Technological Aspects-A Review. Nutrients, 18(13), 2084. https://doi.org/10.3390/nu18132084
18. Ahmed, D. A. E. A., Slima, D. F., Al-Yasi, H. M., Hassan, L. M., & Galal, T. M. (2023). Risk assessment of trace metals in Solanum lycopersicum L.(tomato) grown under wastewater irrigation conditions. Environmental Science and Pollution Research, 30(14), 42255-42266. https://doi.org/10.1007/s11356-023-25157-8
19.Yang, X., Li, J., Zheng, Y., Li, H., & Qiu, R. (2023). Salinity elevates Cd bioaccumulation of sea rice cultured under co-exposure of cadmium and salt. Journal of Environmental Sciences, 126, 602-611. https://doi.org/10.1016/j.jes.2022.05.053
20. Goussi, R., Manaa, A., Derbali, W., Ghnaya, T., Abdelly, C., & Barbato, R. (2018). Combined effects of NaCl and Cd2+ stress on the photosynthetic apparatus of Thellungiella salsuginea. Biochimica et Biophysica Acta (BBA)-Bioenergetics, 1859(12), 1274-1287. https://doi.org/10.1016/j.bbabio.2018.10.001
21. Han, W., Qina, H., Yan, Z., Guosheng, S., Yijun, H., & Youxiang, X. (2024). Biochar decreases soil cadmium (Cd) availability and regulates expression levels of Cd uptake/transport-related genes to reduce Cd translocation in rice. Rice Science, 31(5), 494. https://doi.org/10.1016/j.rsci.2024.04.004
22. Choudhary, Yogesh, Sonal Mathur, and Anjana Jajoo. "Beneficial networking between AMF and plants leads to improved stress tolerance." Discover Plants 3.1 (2026): 30. https://doi.org/10.1007/s44372-026-00494-3
23. Ndiate, N. I., Saeed, Q., Haider, F. U., Liqun, C., Nkoh, J. N., & Mustafa, A. (2021). Co-application of biochar and arbuscular mycorrhizal fungi improves salinity tolerance, growth and lipid metabolism of maize (Zea mays L.) in an alkaline soil. Plants, 10(11), 2490. https://doi.org/10.3390/plants10112490
24. Oluwasiji, I., Samuel, A., Solomon, A., & Oluwagbotemi, F. (2026). Combined Application of Biochar and Arbuscular Mycorrhizal Fungi Enhances Soil Fertility, Antioxidant Defense, and Growth Performance of Cocoa (Theobroma cacao L.). Journal of Soil, Plant and Environment, 5(2), 14-25. https://doi.org/10.56946/jspae.v5i2.871
25. Fang, X., Lee, X., Twagirayezu, G., Cheng, H., Lu, H., Huang, S., & Ji, B. (2024). A critical review of the effectiveness of biochar coupled with arbuscular mycorrhizal fungi in soil cadmium immobilization. Journal of Fungi, 10(3), 182. https://doi.org/10.3390/jof10030182
26. Mustafa, S., Mahmood, F., Hussain, S., & Shahzad, T. (2026). Assessing the synergistic effects of different plant bio-stimulants for amelioration of morpho-physio-biochemical attributes of wheat against cd stress. Water, Air, & Soil Pollution, 237(2), 84. https://doi.org/10.1007/s11270-025-08762-w
27. Ayers, R. S., & Westcot, D. W. (1985). Water quality for agriculture (Vol. 29, p. 174). Rome: Food and agriculture organization of the United Nations.
28. La, R. (1954). Diagnosis and improvement of saline and alkali soils. USDA handbook, 60, 84-156.
29. Lau, C. M., Ure, A. M., & West, T. S. (1983). The determiantion of lead and cadmium in soils by atom-trapping atomic absorption spectrometry. Analytica Chimica Acta, 146, 171-179. https://doi.org/10.1016/S0003-2670(00)80603-0
30. Pedersen, B., Willems, M., & Jørgensen, S. S. (1980). Determination of copper, lead, cadmium, nickel and cobalt in EDTA extracts of soil by solvent extraction and graphite furnace atomic-absorption spectrophotometry. Analyst, 105(1247), 119-124. https://doi.org/10.1039/an9800500119
31. Anderson, J. P., & Domsch, K. H. (1978). A physiological method for the quantitative measurement of microbial biomass in soils. Soil biology and biochemistry, 10(3), 215-221. https://doi.org/10.1016/0038-0717(78)90099-8
32. Casida Jr, L. E., Klein, D. A., & Santoro, T. (1964). Soil dehydrogenase activity. Soil science, 98(6), 371-376. https://doi.org/10.1097/00010694-196412000-00004
33.Tabatabai, M. A., & Bremner, J. M. (1969). Use of p-nitrophenyl phosphate for assay of soil phosphatase activity. Soil biology and biochemistry, 1(4), 301-307. https://doi.org/10.1016/0038-0717(69)90012-1
34. Allen, S. E., Grimshaw, H. M., Parkinson, J. A., & Quarmby, C. (1974). Chemical analysis of ecological materials (pp. xii+-565).
35. Jones Jr, J. B. (2001). Laboratory guide for conducting soil tests and plant analysis. CRC press. https://doi.org/10.1201/9781420025293
36. Alici, E.H.; Arabaci, G. Determination of SOD, POD, PPO and CAT enzyme activities in Rumex obtusifolius L. Annual Research & Review in Biology 2016, 11, 1-7. https://doi.org/10.9734/ARRB/2016/29809
37. Velikova, V., Yordanov, I., & Edreva, A. J. P. S. (2000). Oxidative stress and some antioxidant systems in acid rain-treated bean plants: protective role of exogenous polyamines. Plant science, 151(1), 59-66. https://doi.org/10.1016/S0168-9452(99)00197-1
38. Bates, L. S., Waldren, R. P. A., & Teare, I. D. (1973). Rapid determination of free proline for water-stress studies. Plant and soil, 39(1), 205-207. https://doi.org/10.1007/BF00018060
39. Hodges, D. M., DeLong, J. M., Forney, C. F., & Prange, R. K. (1999). Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta, 207(4), 604-611. https://doi.org/10.1007/s004250050524
40. Shan, C., & Ou, X. (2018). Hydrogen peroxide is involved in the regulation of ascorbate and glutathione metabolism in wheat leaves under water stress. Cereal Research Communications, 46(1), 21-30. https://doi.org/10.1556/0806.45.2017.053
41. Hou, D., O'Connor, D., Igalavithana, A. D., Alessi, D. S., Luo, J., Tsang, D. C., & Ok, Y. S. (2020). Metal contamination and bioremediation of agricultural soils for food safety and sustainability. Nature Reviews Earth & Environment, 1(7), 366-381. https://doi.org/10.1038/s43017-020-0061-y
42. Rahim, H. U., et al. (2022). Biochar for cadmium immobilization in contaminated soil: Mechanisms and influencing factors. Agronomy, 12(4), 877. https://doi.org/10.3390/agronomy12040877
43. Zhang, F., Hu, B., Meng, L., Pang, M., Chen, Y., Song, W., & Ma, Y. (2025). Appropriate biochar application methods can simultaneously mitigate Cd concentrations in different parts of soil and crops: A meta‐analysis. Soil Use and Management, 41(1), e70044. https://doi.org/10.1111/sum.70044
44. Yang, X., Li, J., Zheng, Y., Li, H., & Qiu, R. (2023). Salinity elevates Cd bioaccumulation of sea rice cultured under co-exposure of cadmium and salt. Journal of Environmental Sciences, 126, 602-611. https://doi.org/10.1016/j.jes.2022.05.053
45. Goussi, R., Manaa, A., Derbali, W., Ghnaya, T., Abdelly, C., & Barbato, R. (2018). Combined effects of NaCl and Cd2+ stress on the photosynthetic apparatus of Thellungiella salsuginea. Biochimica et Biophysica Acta (BBA)-Bioenergetics, 1859(12), 1274-1287. https://doi.org/10.1016/j.bbabio.2018.10.001
46.Roșca, M., Mihalache, G., & Stoleru, V. (2023). Tomato responses to salinity stress: From morphological traits to genetic changes. Frontiers in plant science, 14, 1118383. https://doi.org/10.3389/fpls.2023.1118383
47. Sachdeva, S., Kumar, R., Sahoo, P. K., & Nadda, A. K. (2023). Recent advances in biochar amendments for immobilization of heavy metals in an agricultural ecosystem: A systematic review. Environmental pollution, 319, 120937. https://doi.org/10.1016/j.envpol.2022.120937
48. Gong, X., Huang, D., Liu, Y., Zeng, G., Wang, R., Wan, J., Zhang, C., Cheng, M., Qin, X., & Xue, W. (2022). Biochar-based remediation of heavy metals in contaminated soils: A review of mechanisms and applications. Journal of Hazardous Materials, 424, 127668. https://doi.org/10.1016/j.jhazmat.2022.128668
49. Sani, Z. K., Shah, T., Basiru, S., Salmon, M. A., Radouane, N., Legeay, J., & Hijri, M. (2026). Arbuscular mycorrhizal fungi mitigate cadmium toxicity in plants: A global meta-analysis. Mycorrhiza, 36(1), 2. https://doi.org/10.1007/s00572-025-01246-z
50. Zhao, S., Yan, L., Kamran, M., Liu, S., & Riaz, M. (2024). Arbuscular mycorrhizal fungi-assisted phytoremediation: A promising strategy for cadmium-contaminated soils. Plants, 13(23), 3289. https://doi.org/10.3390/plants13233289
51.Abid, M., Danish, S., Zafar-ul-Hye, M., Shaaban, M., Iqbal, M. M., Rehim, A., & Naqqash, M. N. (2017). Biochar increased photosynthetic and accessory pigments in tomato (Solanum lycopersicum L.) plants by reducing cadmium concentration under various irrigation waters. Environmental Science and Pollution Research, 24(27), 22111-22118. https://doi.org/10.1007/s11356-017-9866-8
52. Garg, N., & Chandel, S. (2010). Arbuscular mycorrhizal networks: process and functions. A review. Agronomy for Sustainable Development, 30(3), 581-599. https://doi.org/10.1051/agro/2009054
53. Ali, I., He, L., Ullah, S., Quan, Z., Wei, S., Iqbal, A., & Ligeng, J. (2020). Biochar addition coupled with nitrogen fertilization impacts on soil quality, crop productivity, and nitrogen uptake under double‐cropping system. Food and Energy Security, 9(3), e208. https://doi.org/10.1002/fes3.208
54. Danso, O. P., Acheampong, A., Zhang, Z., Song, J., Wang, Z., Dai, J., & Zhu, R. (2023). The management of Cd in rice with biochar and selenium: effects, efficiency, and practices. Carbon research, 2(1), 41. https://doi.org/10.1007/s44246-023-00073-1
55. Shah, S., Khan, Y., Wang, M., & Zhang, T. (2026). Arbuscular mycorrhizal fungi as mediators of nitrogen, phosphorus, and carbon: implications for plant growth and development. Journal of Plant Nutrition, 49(4), 687-707. https://doi.org/10.1080/01904167.2025.2563296
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