• Abstract

    An effective, practical, and sustainable nutritional crop supplementation strategy for crops is achievable through the application of biostimulants, which can also mitigateenvironmental issues associated with excessive fertilization. Plants benefit from biostimulants when their metabolism is increased, which leads to higher yields and improved quality crops; it protects plants from stress caused by water shortage, soil salinization, and suboptimal growth temperatures; and it promotes plant growth by increasing nutrient absorption. In addition, it enhances soil fertility by nurturing the development of complementary soil microbes, enhancing soil enzymatic and microbial activity, changing root architecture, enhancing micronutrient solubility and mobility, and changing root architecture. It is possible to categorize biostimulants as microbial, such as arbuscular mycorrhizae fungi (AMF), plant-growth-promoting rhizobacteria (PGPR), nonpathogenic fungi, protozoa, and nematodes, or nonmicrobial, such as seaweed extract, phosphite, humic acid, other inorganic salts, chitin and chitosan derivatives, protein hydrolysates, free amino acids, and complex organic materials. It is important for sustainable agriculture to cultivate better, healthier, and more functional foods with the help of arbuscular mycorrhizal fungi, which are among the best known microbial biostimulants. As a sustainable and environmentally friendly source of crop supplements, AMF helps plants acquire nutrients and water, improves plant stress tolerance for salinity, drought, and heavy metals, and reduces soil erosion. To better understand how biostimulants can be used in sustainable agriculture, further studies are needed. Several examples of how biostimulants can be used to produce various crops are presented in the current manuscript. This review presents examples of biostimulant applications in various crops and discusses the role of AMF in bridging yield gaps between organic and conventional farming by improving nutrient availability, uptake, and assimilation, thus addressing the nutrient limitations often found in organic systems.

  • References

    1. Aalipour, H., Nikbakht, A., Etemadi, N., Rejali, F., & Soleimani, M. (2020). Biochemical response and interactions between arbuscular mycorrhizal fungi and plant growth promoting rhizobacteria during establishment and stimulating growth of Arizona cypress (Cupressus arizonica G.) under drought stress. Scientia Horticulturae, 261, 108923. https://doi.org/10.1016/j.scienta.2019.108923
    2. Ahemad, M., & Kibret, M. (2014). Mechanisms and applications of plant growth promoting rhizobacteria: Current perspective. Journal of King Saud University - Science, 26(1), 1–20. https://doi.org/10.1016/j.jksus.2013.05.001
    3. Albertsen, A., Ravnskov, S., Green, H., Jensen, D. F., & Larsen, J. (2006). Interactions between the external mycelium of the mycorrhizal fungus Glomus intraradices and other soil microorganisms as affected by organic matter. Soil Biology and Biochemistry, 38(5), 1008–1014. https://doi.org/10.1016/j.soilbio.2005.08.015
    4. Alfonzetti, M., Doleac, S., Mills, C. H., Gallagher, R. V., & Tetu, S. (2023). Characterizing effects of microbial biostimulants and whole-soil inoculums for native plant revegetation. Microorganisms, 11(1), 55. https://doi.org/10.3390/microorganisms11010055
    5. Ali, B. (2021). Salicylic acid: An efficient elicitor of secondary metabolite production in plants. Biocatalysis and Agricultural Biotechnology, 31, 101884. https://doi.org/10.1016/j.bcab.2020.101884
    6. Alves de Assis, R. M., Carneiro, J. J., Medeiros, A. P. R., Carvalho, A. A. D., Honorato, A. D. C., Carneiro, M. A. C., Bertolucci, S. K. V., & Pinto, J. E. B. P. (2020). Arbuscular mycorrhizal fungi and organic manure enhance growth and accumulation of citral, total phenols, and flavonoids in Melissa officinalis L. Industrial Crops and Products, 158, 112981. https://doi.org/10.1016/j.indcrop.2020.112981
    7. Anbarasi, D., & Haripriya, K. (2020). Response of aggregatum onion (Allium cepa L. var. aggregatum Don.) to organic inputs, biofertilizer and biostimulants. Plant Archives, 20(2), 759–762. https://doi.org/10.1016/j.indcrop.2020.112981
    8. Anli, M., Baslam, M., Tahiri, A., Raklami, A., Symanczik, S., Boutasknit, A., Ait-El-Mokhtar, M., Ben-Laouane, R., Toubali, S., & Ait Rahou, Y. (2020). Biofertilizers as strategies to improve photosynthetic apparatus, growth, and drought stress tolerance in date palm. Frontiers in Plant Science, 11, 516818. https://doi.org/10.3389/fpls.2020.516818
    9. Anton-Herrero, R., Garcia-Delgado, C., Anton-Herrero, G., Mayans, B., Delgado-Moreno, L., & Eymar, E. (2023). Design of a hydroponic test to evaluate the biostimulant potential of new organic and organomineral products. Scientia Horticulturae, 310, 111753. https://doi.org/10.1016/j.scienta.2022.111753
    10. Arkhipova, T. N., Veselov, S. U., Melentiev, A. I., Martynenko, E. V., & Kudoyarova, G. R. (2005). Ability of bacterium Bacillus subtilis to produce cytokinins and to influence the growth and endogenous hormone content of lettuce plants. Plant and Soil, 272(1–2), 201–209. https://doi.org/10.1007/s11104-004-5047-x
    11. Aroca, R., Rosa, P., & Ruiz-Lozano, J. M. (2007). How does arbuscular mycorrhizal symbiosis regulate root hydraulic properties and plasma membrane aquaporins in Phaseolus vulgaris under drought, cold or salinity stresses? New Phytologist, 173(4), 808–816. https://doi.org/10.1111/j.1469-8137.2006.01961.x
    12. Askari-Khorasgani, O., Hatterman-Valenti, H., Pardo, F. B. F., & Pessarakli, M. (2019). Plant and symbiont metabolic regulation and biostimulants application improve symbiotic performance and cold acclimation. Journal of Plant Nutrition, 42(17), 2151–2163. https://doi.org/10.1080/01904167.2019.1648681
    13. Asrar, A.-W. A., & Elhindi, K. M. (2011). Alleviation of drought stress of marigold (Tagetes erecta) plants by using arbuscular mycorrhizal fungi. Saudi Journal of Biological Sciences, 18(1), 93–98. https://doi.org/10.1016/j.sjbs.2010.06.007
    14. Azizi, S., Kouchaksaraei, M. T., Hadian, J., Nosrat Abad, A. R., Sanavi, S. A. M. M., Ammer, C., & Bader, M. K.-F. (2021). Dual inoculation of arbuscular mycorrhizal fungi and plant growth-promoting rhizobacteria boost drought resistance and essential oil yield of common myrtle. Forest Ecology and Management, 497, 119478. https://doi.org/10.1016/j.foreco.2021.119478
    15. Bacilio, M., Rodriguez, H., Moreno, M., Hernandez, J. P., & Bashan, Y. (2004). Mitigation of salt stress in wheat seedlings by a gfp-tagged Azospirillum lipoferum. Biology and Fertility of Soils, 40(3), 188–193. https://doi.org/10.1007/s00374-004-0757-z
    16. Baczek, K. B., Wisniewska, M., Przybyl, J. L., Kosakowska, O., & Weglarz, Z. (2019). Arbuscular mycorrhizal fungi in chamomile (Matricaria recutita L.) organic cultivation. Industrial Crops and Products, 140, 111562. https://doi.org/10.1016/j.indcrop.2019.111562
    17. Bae, H., Sicher, R. C., Kim, M. S., Kim, S.-H., Strem, M. D., Melnick, R. L., & Bailey, B. A. (2009). The beneficial endophyte Trichoderma hamatum isolate DIS 219b promotes growth and delays the onset of the drought response in Theobroma cacao. Journal of Experimental Botany, 60(11), 3279–3295. https://doi.org/10.1093/jxb/erp165
    18. Barnawal, D., Bharti, M., Maji, D., Chanotiya, C. S., & Kalra, A. (2014). ACC deaminase-containing Arthrobacter protophormiae induces NaCl stress tolerance through reduced ACC oxidase activity and ethylene production resulting in improved nodulation and mycorrhization in Pisum sativum. Journal of Plant Physiology, 171(11), 884–894. https://doi.org/10.1016/j.jplph.2014.03.007
    19. Bashan, Y., & Holguin, G. (1998). Proposal for division of plant growth promoting rhizobacteria into two classifications: Biocontrol-PGPB (Plant growth-promoting bacteria) and PGPB. Soil Biology and Biochemistry, 30(8), 1225–1228. https://doi.org/10.1016/S0038-0717(97)00187-9
    20. Begum, N., Qin, C., Ahanger, M. A., Raza, S., Khan, M. I., Ashraf, M., Ahmed, N., & Zhang, L. (2019). Role of arbuscular mycorrhizal fungi in plant growth regulation: Implications in abiotic stress tolerance. Frontiers in Plant Science, 10, 1068. https://doi.org/10.3389/fpls.2019.01068
    21. Behera, B., Supraja, K. V., & Paramasivan, B. (2021). Integrated microalgal biorefinery for the production and application of biostimulants in circular bioeconomy. Bioresource Technology, 339, 125588. https://doi.org/10.1016/j.biortech.2021.125588
    22. Berg, G. (2009). Plant-microbe interactions promoting plant growth and health: Perspectives for controlled use of microorganisms in agriculture. Applied Microbiology and Biotechnology, 84(1), 11–18. https://doi.org/10.1007/s00253-009-2092-7
    23. Betancur-Agudelo, M., Meyer, E., & Lovato, P. E. (2023). Increased copper concentrations in soil affect indigenous arbuscular mycorrhizal fungi and physiology of grapevine plantlets. Rhizosphere, 27, 100711. https://doi.org/10.1016/j.rhisph.2023.100711
    24. Bosi, S., Negri, L., Accorsi, M., Baffoni, L., Gaggia, F., Gioia, D. D., Dinelli, G., & Marotti, I. (2023). Biostimulants for sustainable management of sport turfgrass. Plants, 12(3), 539. https://doi.org/10.3390/plants12030539
    25. Botti, A., Musmeci, E., Negroni, A., Capuozzo, R., Fava, F., Biagi, E., & Zanaroli, G. (2023). Site-specific response of sediment microbial community to supplementation of polyhydroxyalkanoates as biostimulants for PCB reductive dechlorination. Science of the Total Environment, 898, 165485. https://doi.org/10.1016/j.scitotenv.2023.165485
    26. Boyer, L. R., Brain, P., Xu, X. M., & Jeffries, P. (2015). Inoculation of drought-stressed strawberry with a mixed inoculum of two arbuscular mycorrhizal fungi: Effects on population dynamics of fungal species in roots and consequential plant tolerance to water deficiency. Mycorrhiza, 25(3), 215–227. https://doi.org/10.1007/s00572-014-0603-6
    27. Bozhinova, R. (2023). Yield and chemical composition of oriental tobacco as affected by biostimulant application. Bulgarian Journal of Agricultural Science, 29(1), 89–96. https://www.agrojournal.org/29/01-10.pdf
    28. Cacciari, I., & Lippi, D. (1987). Arthrobacters: Successful arid soil bacteria: A review. Arid Soil Research and Rehabilitation, 1(1), 1–30. https://doi.org/10.1080/15324988709381125
    29. Calvo, P., Nelson, L., & Kloepper, J. W. (2014). Agricultural uses of plant biostimulants. Plant and Soil, 383(1–2), 3–41. https://doi.org/10.1007/s11104-014-2131-8
    30. Calvo-Polanco, M., Sanchez-Romera, B., Aroca, R., Asins, M. J., Declerck, S., Dodd, I. C., Martinez-Andujar, C., Albacete, A., & Ruiz-Lozano, J. M. (2016). Exploring the use of recombinant inbred lines in combination with beneficial microbial inoculants (AM fungus and PGPR) to improve drought stress tolerance in tomato. Environmental and Experimental Botany, 131, 47–57. https://doi.org/10.1016/j.envexpbot.2016.06.015
    31. Canellas, L. P., Olivares, F. L., Aguiar, N. O., Jones, D. L., Nebbioso, A., Mazzeri, P., & Piccolo, A. (2015). Humic and fulvic acids as biostimulants in horticulture. Scientia Horticulturae, 196, 15–27. https://research-repository.uwa.edu.au/en/publications/humic-and-fulvic-acids-as-biostimulants-in-horticulture
    32. Carillo, P., Kyratzis, A., Kyriacou, M. C., Dell’Aversana, E., Fusco, G. M., Corrado, G., & Rouphael, Y. (2020). Biostimulatory action of arbuscular mycorrhizal fungi enhances productivity, functional and sensory quality in Piennolo del Vesuvio cherry tomato landraces. Agronomy, 10(6), 911. https://doi.org/10.3390/agronomy10060911
    33. Celebi, S. Z., Demir, S., Celebi, R., Durak, E. D., & Yilmaz, I. H. (2010). The effect of arbuscular mycorrhizal fungi (AMF) applications on the silage maize (Zea mays L.) yield in different irrigation regimes. European Journal of Soil Biology, 46(5), 302–305. https://doi.org/10.1016/j.ejsobi.2010.06.002
    34. Chen, E. C. H., Morin, E., Beaudet, D., Noel, J., Yildirir, G., Ndikumana, S., Charron, P., St-Onge, C., Giorgi, J., & Kruger, M. (2018). High intraspecific genome diversity in the model arbuscular mycorrhizal symbiont Rhizophagus irregularis. New Phytologist, 220(4), 1161–1171. https://doi.org/10.1111/nph.14989
    35. Chen, K., Kleijn, D., Scheper, J., & Fijen, T. P. M. (2022). Additive and synergistic effects of arbuscular mycorrhizal fungi, insect pollination and nutrient availability in a perennial fruit crop. Agriculture, Ecosystems & Environment, 325, 107742. https://doi.org/10.1016/j.agee.2021.107742
    36. Cheng, X.-F., Xie, M.-M., Li, Y., Liu, B.-Y., Liu, C.-Y., Wu, Q.-S., & Kuca, K. (2022). Effects of field inoculation with arbuscular mycorrhizal fungi and endophytic fungi on fruit quality and soil properties of Newhall navel orange. Applied Soil Ecology, 170, 104308. https://doi.org/10.1016/j.apsoil.2021.104308
    37. Costa, O. Y. A., Pijl, A., Houbraken, J., van Lith, W., & Kuramae, E. E. (2023). Soil substrate source drives the microbes involved in the degradation of gelatin used as a biostimulant. Applied Soil Ecology, 189, 104906. https://pure.knaw.nl/ws/portalfiles/portal/907543995/Costa_et_al_2023.pdf
    38. Cruz, C., Vishwakarma, K., Kumar, D., & Varma, A. (2021). Soil Nitrogen Ecology. Springer Nature Switzerland AG. https://doi.org/10.1007/978-3-030-71206-8
    39. Cui, X., Jia, B., Diao, F., Li, X., Xu, J., Zhang, Z., Li, F. Y., & Guo, W. (2022). Transcriptomic analysis reveals the molecular mechanisms of arbuscular mycorrhizal fungi and nitrilotriacetic acid on Suaeda salsa tolerance to combined stress of cadmium and salt. Process Safety and Environmental Protection, 160, 210–220. https://doi.org/10.1016/j.psep.2022.02.019
    40. Dal Cortivo, C., Barion, G., Visioli, G., Mattarozzi, M., Mosca, G., & Vamerali, T. (2017). Increased root growth and nitrogen accumulation in common wheat following PGPR inoculation: Assessment of plant-microbe interactions by ESEM. Agriculture, Ecosystems & Environment, 247, 396–408. https://air.unipr.it/retrieve/e177fbc5-aa77-50b0-e053-d805fe0adaee/AGEE_proof.pdf
    41. Dal Cortivo, C., Ferrari, M., Visioli, G., Lauro, M., Fornasier, F., Barion, G., Panozzo, A., & Vamerali, T. (2020). Effects of seed-applied biofertilizers on rhizosphere biodiversity and growth of common wheat (Triticum aestivum L.) in the field. Frontiers in Plant Science, 11, 1–14. https://doi.org/10.3389/fpls.2020.00072
    42. Dalmastri, C., Chiarini, L., Cantale, C., Bevivino, A., & Tabacchioni, S. (1999). Soil type and maize cultivar affect the genetic diversity of maize root-associated Burkholderia cepacia populations. Microbial Ecology, 38(3), 273–284. https://doi.org/10.1007/s002489900177
    43. Elhindi, K. M., El-Din, A. S., & Elgorban, A. M. (2017). The impact of arbuscular mycorrhizal fungi in mitigating salt-induced adverse effects in sweet basil (Ocimum basilicum L.). Saudi Journal of Biological Sciences, 24(1), 170–179. https://doi.org/10.1016/j.sjbs.2016.02.010
    44. Fahsi, N., Mahdi, I., Mesfioui, A., Biskri, L., & Allaoui, A. (2021). Plant growth-promoting rhizobacteria isolated from the jujube (Ziziphus lotus) plant enhance wheat growth, Zn uptake, and heavy metal tolerance. Agriculture, 11(4), 316. https://doi.org/10.3390/agriculture11040316
    45. Falcao, E. L., Muniz, B. C., Filho, C. J. A. B., Kapoor, R., & da Silva, F. S. B. (2023). Soil microbial respiration and pH modulated by arbuscular mycorrhizal fungi influence the biosynthesis of health-promoting compounds in Anadenanthera colubrina (Vell.) Brenan. Rhizosphere, 26, 100685. https://doi.org/10.1016/j.rhisph.2023.100685
    46. Ganugi, P., Martinelli, E., & Lucini, L. (2021). Microbial biostimulants as a sustainable approach to improve the functional quality in plant-based foods: A review. Current Opinion in Food Science, 41, 217–223. https://doi.org/10.1016/j.cofs.2021.05.001
    47. Ghadbane, M., Medjekal, S., Benderradji, L., Belhadj, H., & Daoud, H. (2021). Assessment of arbuscular mycorrhizal fungi status and rhizobium on date palm (Phoenix dactylifera L.) cultivated in a Pb contaminated soil. In Recent Advances in Environmental Science from the Euro-Mediterranean and Surrounding Regions (2nd ed., pp. 703–707). Springer. https://doi.org/10.1007/978-3-030-51210-1_111
    48. Goicoechea, N., & Antolin, M. C. (2017). Increased nutritional value in food crops. Microbiology and Biotechnology, 10(6), 1004–1007. https://doi.org/10.1111/1751-7915.12764
    49. Goni, O., Quille, P., & O’Connell, S. (2016). Production of chitosan oligosaccharides for inclusion in a plant biostimulant. Pure and Applied Chemistry, 88(9), 881–889. https://doi.org/10.1515/pac-2016-0701
    50. Guo, X., Liu, H., & Wu, S. (2019). Humic substances developed during organic waste composting: Formation mechanisms, structural properties, and agronomic functions. Science of the Total Environment, 662, 501–510. https://doi.org/10.1016/j.scitotenv.2019.01.137
    51. Hajiboland, R., Dashtebani, F., & Aliasgharzad, N. (2015). Physiological responses of halophytic C4 grass Aeluropus littoralis to salinity and arbuscular mycorrhizal fungi colonization. Photosynthetica, 53(4), 572–584. https://doi.org/10.1007/s11099-015-0131-4
    52. Halpern, M., Bar-Tal, A., Ofek, M., Minz, D., Muller, T., & Yermiyahu, U. (2015). The use of biostimulants for enhancing nutrient uptake. Advances in Agronomy, 130, 141–174. https://link.springer.com/collections/ecdeiaeegb?gad_source=1&gclid=CjwKCAiAjeW6BhBAEiwAdKltMrmC8juVvaZHC-Rhytuvofu1zBj6k_kfcboX9dB1z3_WQTAiOrmQyxoCiBUQAvD_BwE
    53. Hart, M. M., & Reader, R. J. (2002). Taxonomic basis for variation in the colonization strategy of arbuscular mycorrhizal fungi. New Phytologist, 153(2), 335–344. https://doi.org/10.1046/j.0028-646X.2001.00312.x
    54. Hasani, H., & Aminpanah, H. (2015). Effect of Pseudomonas fluorescens inoculation on yield and yield components of rice (Oryza sativa L.) under different levels of phosphorus fertilizer. Journal of Agricultural Science, 48(2), 157–163. https://www.cabidigitallibrary.org/doi/pdf/10.5555/20173217358
    55. Hashem, A., Abd-Allah, E. F., Alqarawi, A. A., Al-Huqail, A. A., & Shah, M. A. (2016). Induction of osmoregulation and modulation of salt stress in Acacia gerrardii Benth. by arbuscular mycorrhizal fungi and Bacillus subtilis (BERA 71). BioMed Research International, 2016, 6294098. https://doi.org/10.1155/2016/6294098
    56. Hashiba, T., & Narisawa, K. (2005). The development and endophytic nature of the fungus Heteroconium chaetospira. FEMS Microbiology Letters, 252(2), 191–196. https://doi.org/10.1016/j.femsle.2005.08.039
    57. Hassena, A. B., Zouari, M., Trabelsi, L., Decou, R., Amar, F. B., Chaari, A., Sousa, N., Labrousse, P., Khabou, W., & Zouari, N. (2021). Potential effects of arbuscular mycorrhizal fungi in mitigating the salinity of treated wastewater in young olive plants (Olea europaea L. cv. Chetoui). Agricultural Water Management, 245, 106635. https://doi.org/10.1016/j.agwat.2020.106635
    58. Hu, J.-L., Lin, X.-G., Wang, J.-H., Shen, W.-S., Wu, S., Peng, S.-P., & Mao, T.-T. (2010). Arbuscular mycorrhizal fungal inoculation enhances suppression of cucumber Fusarium wilt in greenhouse soils. Pedosphere, 20(5), 586–593. https://doi.org/10.1016/S1002-0160(10)60048-3
    59. Hussain, A., & Hasnain, S. (2009). Cytokinin production by some bacteria: Its impacts on cell division in cucumber cotyledons. African Journal of Microbiological Research, 3(11), 704–712. https://academicjournals.org/article/article1380369707_Hussain%20and%20Hasnain.pdf
    60. Jacobs-Hoffman, I., & Hills, P. N. (2021). Effects of the commercial biostimulant BC204 on the rhizosphere microbial community of Solanum lycopersicum L. South African Journal of Botany, 143, 52–60. https://doi.org/10.1016/j.sajb.2021.08.011
    61. Jain, D., Sharma, J., Kaur, G., Bhojiya, A. A., Chauhan, S., Sharma, V., Suman, A., Mohanty, S. R., & Maharjan, E. (2021). Phenetic and molecular diversity of nitrogen-fixing plant growth-promoting Azotobacter isolated from semiarid regions of India. BioMed Research International, 2021, 6686283. https://doi.org/10.1155/2021/6686283
    62. Joe, M. M., Devaraj, S., Benson, A., & Sa, T. (2016). Isolation of phosphate solubilizing endophytic bacteria from Phyllanthus amarus Schum & Thonn: Evaluation of plant growth promotion and antioxidant activity under salt stress. Journal of Applied Research on Medicinal and Aromatic Plants, 3(2), 71–77. https://doi.org/10.1016/j.jarmap.2016.02.003
    63. Joly, P., Calteau, A., Wauquier, A., Dumas, R., Beuvin, M., Vallenet, D., Crovadore, J., Cochard, B., Lefort, F., & Berthon, J.-Y. (2021). From strain characterization to field authorization: Highlights on Bacillus velezensis strain B2 beneficial properties for plants and its activities on phytopathogenic fungi. Microorganisms, 9(9), 1924. https://doi.org/10.3390/microorganisms9091924
    64. Kan, Z.-R., Wei, Q., Yang, R., Li, Y., Zhou, J., Qi, J., Li, F.-M., & Yang, H. (2023). Arbuscular mycorrhizal fungi mitigate earthworm-induced N2O emissions from upland soil in a rice-rotated wheat farming system. Applied Soil Ecology, 189, 104981. https://ui.adsabs.harvard.edu/abs/2023AppSE.18904981K/abstract
    65. Karapouloutidou, S., & Gasparatos, D. (2019). Effects of biostimulant and organic amendment on soil properties and nutrient status of Lactuca sativa in a Calcareous saline-sodic soil. Agriculture, 9(8), 164. https://doi.org/10.3390/agriculture9080164
    66. Karthikeyan, B., Abitha, B., Henry, A. J., Sa, T., & Joe, M. M. (2016). Interaction of rhizobacteria with arbuscular mycorrhizal fungi (AMF) and their role in stress abatement in agriculture. In Fungal Biology (pp. 117–142). Springer. https://doi.org/10.1007/978-3-319-24355-9_11
    67. Katenkamp, U., Jacob, H.-E., Kerns, G., & Dalchow, E. (1989). Hybridization of Trichoderma reesei protoplasts by electrofusion. Bioelectrochemistry and Bioenergetics, 22(1), 57–67. https://doi.org/10.1016/0302-4598(89)85030-5
    68. Kaushal, P., Ali, N., Saini, S., Pati, P. K., & Pati, A. M. (2023). Physiological and molecular insight of microbial biostimulants for sustainable agriculture. Frontiers in Plant Science, 14, 1041413. https://doi.org/10.3389/fpls.2023.1041413
    69. Khaksar, G., Treesubsuntorn, C., & Thiravetyan, P. (2017). Impact of endophytic colonization patterns on Zamioculcas zamiifolia stress response and in regulating ROS, tryptophan and IAA levels under airborne formaldehyde and formaldehyde-contaminated soil conditions. Plant Physiology and Biochemistry, 114, 1–9. https://doi.org/10.1016/j.plaphy.2017.02.016
    70. Khalid, A., Arshad, M., & Zahir, Z. A. (2004). Screening plant growth-promoting rhizobacteria for improving growth and yield of wheat. Journal of Applied Microbiology, 96(3), 473–480. https://doi.org/10.1046/j.1365-2672.2003.02161.x
    71. Khalloufi, M., Martinez-Andujar, C., Lachaal, M., Karray-Bouraoui, N., Perez-Alfocea, F., & Albacete, A. (2017). The interaction between foliar GA3 application and arbuscular mycorrhizal fungi inoculation improves growth in salinized tomato (Solanum lycopersicum L.) plants by modifying the hormonal balance. Journal of Plant Physiology, 214, 134–144. https://doi.org/10.1016/j.jplph.2017.04.012
    72. Kimura, T., Ueno, M., Petchsang, N., & Nishiyama, K. (2023). Barley uptake of ZnO nanoparticles enhanced by arbuscular mycorrhizal fungi: Implications for biomarker systems. Journal of Molecular Liquids, 386, 122496. https://doi.org/10.3390/plants12173101
    73. Koleska, I., Hasanagic, D., Todorovic, V., Murtic, S., Klokic, I., Paradikovic, N., & Kukavica, B. (2017). Biostimulants prevent yield loss and reduce oxidative damage in tomato plants grown on reduced NPK nutrition. Journal of Plant Interactions, 12(1), 209–218. https://doi.org/10.3390/horticulturae9030348
    74. Krishna, H., Singh, S. K., Sharma, R. R., Khawale, R. N., Grover, M., & Patel, V. B. (2005). Biochemical changes in micropropagated grape (Vitis vinifera L.) plantlets due to arbuscular-mycorrhizal fungi (AMF) inoculation during ex vitro acclimatization. Scientia Horticulturae, 106(4), 554–567. https://doi.org/10.1016/j.scienta.2005.05.009
    75. Kumar, M., Ahmad, S., & Singh, R. (2022). Plant growth promoting microbes: Diverse roles for sustainable and ecofriendly agriculture. Energy Nexus, 7, 100133. https://doi.org/10.1016/j.nexus.2022.100133
    76. Li, Z., Wu, S., Liu, Y., Yi, Q., Hall, M., Saha, N., Wang, J., Huang, Y., & Huang, L. (2023). Arbuscular mycorrhizal fungi regulate plant mineral nutrient uptake and partitioning in iron ore tailings undergoing eco-engineered pedogenesis. Pedosphere. https://doi.org/10.1016/j.pedsph.2023.04.004550
    77. Liang, M., Wu, Y., Zhao, Q., Jiang, Y., Sun, W., Liu, G., Ma, L., & Xue, S. (2023). Secondary vegetation succession on the Loess Plateau altered the interaction between arbuscular mycorrhizal fungi and nitrogen-fixing bacteria. Forest Ecology and Management, 530, 120744. https://doi.org/10.1016/j.foreco.2022.120744
    78. Lin, H.-R., Shu, H.-Y., & Lin, G.-H. (2018). Biological roles of indole-3-acetic acid in Acinetobacter baumannii. Microbiological Research, 216, 30–39. https://doi.org/10.1016/j.micres.2018.08.004
    79. Lindow, S. E., & Brandl, M. T. (2003). Microbiology of the phyllosphere. Applied and Environmental Microbiology, 69(4), 1875–1883. https://doi.org/10.1128/AEM.69.4.1875-1883.2003
    80. Liu, L.-Z., Gong, Z.-Q., Zhang, Y.-L., & Li, P.-J. (2011). Growth, cadmium accumulation and physiology of marigold (Tagetes erecta L.) as affected by arbuscular mycorrhizal fungi. Pedosphere, 21(3), 319–327. https://doi.org/10.1016/S1002-0160(11)60132-X
    81. Liu, S., Lu, X., Yang, G., He, C., Shi, Y., Li, C., Liu, S., Wang, Y., Wang, Z., & Chen, L. (2023). Variation of arbuscular mycorrhizal fungi communities in the rhizosphere soil of Eucalyptus plantations based on different stand ages and its effect on phosphorus fractionation. Applied Soil Ecology, 189, 104908. https://doi.org/10.3390/jof10060404
    82. Lu, N., Zhou, X., Cui, M., Yu, M., Zhou, J., Qin, Y., & Li, Y. (2015). Colonization with arbuscular mycorrhizal fungi promotes the growth of Morus alba L. seedlings under greenhouse conditions. Forests, 6(3), 734–747. https://doi.org/10.3390/f6030734
    83. Lucini, L., Rouphael, Y., Cardarelli, M., Canaguier, R., Kumar, P., & Colla, G. (2015). The effect of a plant-derived biostimulant on metabolic profiling and crop performance of lettuce grown under saline conditions. Scientia Horticulturae, 182, 124–133. https://doi.org/10.1016/j.scienta.2014.11.022
    84. Lugtenberg, B., & Kamilova, F. (2009). Plant-growth-promoting rhizobacteria. Annual Review of Microbiology, 63, 541–556. https://doi.org/10.1146/annurev.micro.62.081307.162918
    85. Mansoor, S., Sharma, V., Mir, M. A., Mir, J. I., Nabi, S. U., Ahmed, N., Alkahtani, J., Alwahibi, M. S., & Masoodi, K. Z. (2020). Quantification of polyphenolic compounds and relative gene expression studies of phenylpropanoid pathway in apple (Malus domestica Borkh) in response to Venturia inaequalis infection. Saudi Journal of Biological Sciences, 27(12), 3397–3404. https://doi.org/10.1016/j.sjbs.2020.09.007
    86. Mayo, K., Davis, R. E., & Motta, J. (1986). Stimulation of germination of spores of Glomus versiforme by spore-associated bacteria. Mycologia, 78(3), 426–431. https://doi.org/10.2307/3793046
    87. Mehnaz, S., Mirza, M. S., Haurat, J., Bally, R., Normand, P., Bano, A., & Malik, K. A. (2001). Isolation and 16S rRNA sequence analysis of the beneficial bacteria from the rhizosphere of rice. Canadian Journal of Microbiology, 47(2), 110–117. https://doi.org/10.1139/w00-132
    88. Meramo-Hurtado, S. I., & Gonzalez-Delgado, A. D. (2020). Application of techno-economic and sensitivity analyses as decision-making tools for assessing emerging large-scale technologies for production of chitosan-based adsorbents. ACS Omega, 5(29), 17601–17610. https://doi.org/10.1021/acsomega.0c02064
    89. Mirshad, P. P., & Puthur, J. T. (2016). Arbuscular mycorrhizal association enhances drought tolerance potential of promising bioenergy grass (Saccharum arundinaceum Retz.). Environmental Monitoring and Assessment, 188(7), 425. https://doi.org/10.1007/s10661-016-5428-7
    90. Mishra, P. K., Mishra, S., Selvakumar, G., Bisht, S. C., Bisht, J. K., Kundu, S., & Gupta, H. S. (2008). Characterization of a psychrotolerant plant growth promoting Pseudomonas sp. strain PGERs17 (MTCC 9000) isolated from North Western Indian Himalayas. Annals of Microbiology, 58(4), 561–568. https://doi.org/10.1007/BF03175558
    91. Mohandas, S. (2012). Arbuscular mycorrhizal fungi benefit mango (Mangifera indica L.) plant growth in the field. Scientia Horticulturae, 143, 43–48. https://doi.org/10.1016/j.scienta.2012.05.030
    92. Mpongwana, S., Manyevere, A., Mupangwa, J., Mpendulo, C. T., & Mashamaite, C. V. (2023). Optimizing biomass yield of three herbaceous forage legumes through dual inoculation of arbuscular mycorrhizal fungi and rhizobia. South African Journal of Botany, 159, 61–71. https://doi.org/10.1016/j.sajb.2023.06.006
    93. Mrid, R. B., Benmrid, B., Hafsa, J., Boukcim, H., Sobeh, M., & Yasri, A. (2021). Secondary metabolites as biostimulant and bioprotectant agents: A review. Science of the Total Environment, 777, 146204. https://doi.org/10.1016/j.scitotenv.2021.146204
    94. Mukherjee, A., Singh, S., Gaurav, A. K., Chouhan, G. K., Jaiswal, D. K., Pereiro, A. P. D. A., Passari, A. K., Abdel-Azeem, A. M., & Verma, J. P. (2022). Harnessing of phytomicrobiome for developing potential biostimulant consortium for enhancing the productivity of chickpea and soil health under sustainable agriculture. Science of the Total Environment, 836, 155550. https://doi.org/10.1016/j.scitotenv.2022.155550
    95. Mukhia, S., Khatri, A., Acharya, V., & Kumar, R. (2021). Comparative genomics and molecular adaptational analysis of Arthrobacter from Sikkim Himalaya provided insights into its survivability under multiple high-altitude stress. Genomics, 113(1), 151–158. https://doi.org/10.1016/j.ygeno.2020.12.001
    96. Ndiate, N. I., Qun, C. L., & Nkoh, J. N. (2022). Importance of soil amendments with biochar and/or arbuscular mycorrhizal fungi to mitigate aluminum toxicity in tamarind (Tamarindus indica L.) on an acidic soil: A greenhouse study. Heliyon, 8(6), e09009. https://doi.org/10.1016/j.heliyon.2022.e09009
    97. Oosten, M. J. V., Pepe, O., Pascale, S. D., Silletti, S., & Maggio, A. (2017). The role of biostimulants and bioeffectors as alleviators of abiotic stress in crop plants. Chemical and Biological Technologies in Agriculture, 4(1), 5. https://doi.org/10.1186/s40538-017-0089-5
    98. Orlandini, V., Maida, I., Fondi, M., Perrin, E., Papaleo, M. C., Bosi, E., Pascale, D. D., Tutino, M. L., Michaud, L., & Giudice, A. L. (2014). Genomic analysis of three sponge-associated Arthrobacter antarctic strains, inhibiting the growth of Burkholderia cepacia complex bacteria by synthesizing volatile organic compounds. Microbiology Research, 169(7–8), 593–601. https://doi.org/10.3390/plants12173101
    99. Ozyigit, I. I., Kahraman, M. V., & Ercan, O. (2007). Relation between explant age, total phenol and regeneration response in tissue cultured cotton (Gossypium hirsutum L.). African Journal of Biotechnology, 6(1), 3–8. https://academicjournals.org/article/article1379768283_Ozyigit%20et%20al.pdf
    100. Pasbani, B., Salimi, A., Aliasgharzad, N., & Hajiboland, R. (2020). Colonization with arbuscular mycorrhizal fungi mitigates cold stress through improvement of antioxidant defense and accumulation of protecting molecules in eggplants. Scientia Horticulturae, 272, 109575. https://doi.org/10.1016/j.scienta.2020.109575
    101. Paymaneh, Z., Sarcheshmehpour, M., Mohammadi, H., & Hesni, M. A. (2023). Vermicompost and/or compost and arbuscular mycorrhizal fungi are conducive to improving the growth of pistachio seedlings to drought stress. Applied Soil Ecology, 182, 104717. https://doi.org/10.1016/j.apsoil.2022.104717
    102. Perez-Montano, F., Alias-Villegas, C., Bellogin, R., del Cerro, P., Espuny, M., Jimenez-Guerrero, I., Lopez-Baena, F., Ollero, F., & Cubo, T. (2014). Plant growth promotion in cereal and leguminous agricultural important plants: From microorganism capacities to crop production. Microbiology Research, 169(5), 325–336. https://doi.org/10.1016/j.micres.2013.09.011
    103. Petropoulos, S. A., Fernandes, A., Plexida, S., Chrysargyris, A., Tzortzakis, N., Barreira, J. C. M., Barros, L., & Ferreira, I. C. F. R. (2020). Biostimulants application alleviates water stress effects on yield and chemical composition of greenhouse green bean (Phaseolus vulgaris L.). Agronomy, 10(2), 181. https://doi.org/10.3390/agronomy10020181
    104. Philibert, T., Lee, B. H., & Fabien, N. (2017). Current status and new perspectives on chitin and chitosan as functional biopolymers. Applied Biochemistry and Biotechnology, 181(4), 1314–1337. https://doi.org/10.1007/s12010-016-2286-2
    105. Popko, M., Michalak, I., Wilk, R., Gramza, M., Chojnacka, K., & Gorecki, H. (2018). Effect of the new plant growth biostimulants based on amino acids on yield and grain quality of winter wheat. Molecules, 23(2), 470. https://doi.org/10.3390/molecules23020470
    106. Poveda, J., & Baptista, P. (2021). Filamentous fungi as biocontrol agents in olive (Olea europaea L.) diseases: Mycorrhizal and endophytic fungi. Crop Protection, 146, 105672. https://doi.org/10.1016/j.cropro.2021.105672
    107. Rafiee, H., Badi, H. N., Mehrafarin, A., Qaderi, A., Zarinpanjeh, N., Sekara, A., & Zand, E. (2016). Application of plant biostimulants as new approach to improve the biological responses of medicinal plants—A critical review. Journal of Medicinal Plants, 15(59), 6–39. https://www.cabidigitallibrary.org/doi/full/10.5555/20163381771
    108. Razakatiana, A. T. E., Trap, J., Baohanta, R. H., Raherimandimby, M., Le Roux, C., Duponnois, R., Ramanankierana, H., & Becquer, T. (2020). Benefits of dual inoculation with arbuscular mycorrhizal fungi and rhizobia on Phaseolus vulgaris planted in a low-fertility tropical soil. Pedobiologia, 83, 150685. https://doi.org/10.1016/j.pedobi.2020.150685
    109. Redecker, D., Schussler, A., Stockinger, H., Sturmer, S. L., Morton, J. B., & Walker, C. (2013). An evidence-based consensus for the classification of arbuscular mycorrhizal fungi (Glomeromycota). Mycorrhiza, 23(7), 515–531. https://doi.org/10.1007/s00572-013-0486-y
    110. Rungin, S., Indananda, C., Suttiviriya, P., Kruasuwan, W., Jaemsaeng, R., & Thamchaipenet, A. (2012). Plant growth enhancing effects by a siderophore-producing endophytic streptomycete isolated from a Thai jasmine rice plant (Oryza sativa L. cv. KDML105). Antonie van Leeuwenhoek, 102(3), 463–472. https://doi.org/10.1007/s10482-012-9778-z
    111. Saia, S., Corrado, G., Vitaglione, P., Colla, G., Bonini, P., Giordano, M., Stasio, E. D., Raimondi, G., Sacchi, R., & Rouphael, Y. (2021). An endophytic fungi-based biostimulant modulates volatile and non-volatile secondary metabolites and yield of greenhouse basil (Ocimum basilicum L.) through variable mechanisms dependent on salinity stress level. Pathogens, 10(7), 797. https://doi.org/10.3390/pathogens10070797
    112. Sales, L. R., Silva, A. O., Sales, F. R., Rodrigues, T. L., Barbosa, M. V., Santos, J. V. D., Kemmelmeier, K., Siqueira, J. O., & Carneiro, M. A. C. (2022). On-farm inoculation of native arbuscular mycorrhizal fungi improves efficiency in increasing sugarcane productivity in the field. Rhizosphere, 22, 100539. https://doi.org/10.1016/j.rhisph.2022.100539
    113. Schubert, M., Mourad, S., Fink, S., & Schwarze, F. W. M. R. (2005). Ecophysiological responses of the biocontrol agent Trichoderma atroviride (T-15603.1) to combined environmental parameters. Biological Control, 49(1), 84–90. https://doi.org/10.1016/j.biocontrol.2008.12.015
    114. Shahrajabian, M. H., & Sun, W. (2023). Five important seeds in traditional medicine, and pharmacological benefits. Seeds, 2(3), 290–308. https://doi.org/10.3390/seeds2030022
    115. Shahrajabian, M. H., & Sun, W. (2023). Mechanism of action of collagen and epidermal growth factor: A review on theory and research methods. Mini-Reviews in Medicinal Chemistry, 23. https://doi.org/10.2174/1389557523666230816090054
    116. Shahrajabian, M. H., Chaski, C., Polyzos, N., Tzortzakis, N., & Petropoulos, S. A. (2021). Sustainable agriculture systems in vegetable production using chitin and chitosan as plant biostimulants. Biomolecules, 11(6), 819. https://doi.org/10.3390/biom11060819
    117. Shahrajabian, M. H., Cheng, Q., & Sun, W. (2022). The effects of amino acids, phenols and protein hydrolysates as biostimulants on sustainable crop production and alleviated stress. Recent Patents on Biotechnology, 16(4), 319–328. https://doi.org/10.2174/1872208316666220412133749
    118. Shahrajabian, M. H., Petropoulos, S. A., & Sun, W. (2023). Survey of the influences of microbial biostimulants on horticultural crops: Case studies and successful paradigms. Horticulturae, 9(2), 193. https://doi.org/10.2174/1872208316666220412133749
    119. Sharma, A., Shahzad, B., Rehman, A., Bhardwaj, R., Landi, M., & Zheng, B. (2019). Response of phenylpropanoid pathway and the role of polyphenols in plants under abiotic stress. Molecules, 24(13), 2452. https://doi.org/10.3390/molecules24132452
    120. Sharma, M., Saini, I., Kaushik, P., Aldawsari, M. M., Balawi, T., & Alam, P. (2021). Mycorrhizal fungi and Pseudomonas fluorescens application reduces root-knot nematode (Meloidogyne javanica) infestation in eggplant. Saudi Journal of Biological Sciences, 28(7), 3685–3691. https://doi.org/10.1016/j.sjbs.2021.05.054
    121. Shehata, S. A., AbdelGawad, K. F., & Elmogy, M. (2017). Quality and shelf-life of onion bulbs influenced by biostimulants. International Journal of Vegetable Science, 23(4), 362–371. https://doi.org/10.1080/19315260.2017.1298170
    122. Shubler, A., Schwarzott, D., & Walker, C. (2001). A new fungal phylum, the Glomeromycota: Phylogeny and evolution. Mycological Research, 105(12), 1413–1421. https://doi.org/10.1017/S0953756201005196
    123. Singh, L. P., Gill, S. S., & Tuteja, N. (2011). Unraveling the role of fungal symbionts in plant abiotic stress tolerance. Plant Signaling & Behavior, 6(2), 175–191. https://doi.org/10.4161/psb.6.2.14146
    124. Spatafora, J. W., Chang, Y., Benny, G. L., Lazarus, K., Smith, M. E., Berbee, M. L., Bonito, G., Corradi, N., Grigoriev, I., & Gryganskyi, A. (2016). A phylum-level phylogenetic classification of zygomycete fungi based on genome-scale data. Mycologia, 108(5), 1028–1046. https://doi.org/10.3852/16-042
    125. Sun, W., & Shahrajabian, M. H. (2023). Therapeutic potential of phenolic compounds in medicinal plants—Natural health products for human health. Molecules, 28(4), 1845. https://doi.org/10.3390/molecules28041845
    126. Sun, W., Shahrajabian, M. H., Petropoulos, S. A., & Shahrajabian, N. (2023). Developing sustainable agriculture systems in medicinal and aromatic plant production by using chitosan and chitin-based biostimulants. Plants, 12(13), 2469. https://doi.org/10.3390/plants12132469
    127. Tejada, M., Benitez, C., Gomez, I., & Parrado, J. (2011). Use of biostimulants on soil restoration: Effects on soil biochemical properties and microbial community. Applied Soil Ecology, 49(1), 11–17. https://doi.org/10.1016/j.apsoil.2011.07.009
    128. Tsoata, E., Njock, S. R., Youmbi, E., & Nwaga, D. (2015). Early effects of water stress on some biochemical and mineral parameters of mycorrhizal Vigna subterranea (L.) Verdc. (Fabaceae) cultivated in Cameroon. International Journal of Agronomy & Agricultural Research, 7(2), 21–35. https://www.researchgate.net/publication/280839633_Early_effects_of_water_stress_on_some_biochemical_and_mineral_parameters_of_mycorrhizal_Vigna_subterranea_L_Verdc_Fabaceae_cultivated_in_Cameroon_httpwwwinnspubnet_Vol_7_No_2_p_21-35_2015
    129. Vasconsuelo, A., & Boland, R. (2007). Molecular aspects of the early stages of elicitation of secondary metabolites in plants. Plant Science, 172(5), 861–875. https://doi.org/10.1016/j.plantsci.2007.01.006
    130. Wszelaczynska, E., Szczepanek, M., Poberezny, J., & Kazula, M. J. (2019). Effect of biostimulant application and long-term storage on the nutritional value of carrot. Horticultura Brasileira, 37(4), 451–457. https://doi.org/10.1590/s0102-053620190414
    131. Wu, H.-G., Liu, W.-S., Zhu, M., & Li, X.-X. (2018). Research and analysis of 74 bloodstream infection cases of Acinetobacter baumannii and drug resistance. European Review for Medical and Pharmacological Sciences, 22(6), 1782–1786. https://doi.org/10.26355/eurrev_201803_14597
    132. Yadav, V. K., Jha, R. K., Kaushik, P., Altalayan, H., Balawi, T. A., & Alam, P. (2021). Traversing arbuscular mycorrhizal fungi and Pseudomonas fluorescens for carrot production under salinity. Saudi Journal of Biological Sciences, 28(7), 4217–4223. https://doi.org/10.1016/j.sjbs.2021.06.025
    133. Yan, Z., Ma, T., Guo, S., Liu, R., & Li, M. (2021). Leaf anatomy, photosynthesis and chlorophyll fluorescence of lettuce as influenced by arbuscular mycorrhizal fungi under high temperature stress. Scientia Horticulturae, 280, 109933. https://doi.org/10.1016/j.scienta.2021.109933
    134. Yang, H., Zang, Y., Yuan, Y., Tang, J., & Chen, X. (2012). Selectivity by host plants affects the distribution of arbuscular mycorrhizal fungi: Evidence from ITS rDNA sequence metadata. BMC Evolutionary Biology, 12(1), 50. https://doi.org/10.1186/1471-2148-12-50
    135. Yooyongwech, S., Samphumphuang, T., Tisarum, R., Theerawitaya, C., & Cha-Um, S. (2016). Arbuscular mycorrhizal fungi (AMF) improved water deficit tolerance in two different sweet potato genotypes involves osmotic adjustments via soluble sugar and free proline. Scientia Horticulturae, 198, 107–117. https://www.researchgate.net/publication/287200813_Arbuscular_mycorrhizal_fungi_AMF_improved_water_deficit_tolerance_in_two_different_sweet_potato_genotypes_involves_osmotic_adjustments_via_soluble_sugar_and_free_proline
    136. Younes, N. A., Anik, T. R., Rahman, M. M., Wardany, A. A., Dawood, M. F. A., Tran, L.-S. P., Latef, A. A. H. A., & Mostofa, M. G. (2023). Effects of microbial biostimulants (Trichoderma album and Bacillus megaterium) on growth, quality attributes, and yield of onion under field conditions. Heliyon, 9(4), e14203. https://doi.org/10.1016/j.heliyon.2023.e14203
    137. Zamljen, T., Medic, A., Veberic, R., Hudina, M., Grohar, M. C., & Slatnar, A. (2023). Influence of hydrolyzed animal protein-based biostimulant on primary, soluble and volatile secondary metabolism of Genovese and Greek-type basil grown under salt stress. Scientia Horticulturae, 319, 112178. https://doi.org/10.1016/j.scienta.2023.112178
    138. Zhao, R., Guo, W., Bi, M., Guo, J., Wang, L., Zhao, J., & Zhang, J. (2015). Arbuscular mycorrhizal fungi affect the growth, nutrient uptake and water status of maize (Zea mays L.) grown in two types of coal mine spoils under drought stress. Applied Soil Ecology, 88, 41–49. https://doi.org/10.1016/j.apsoil.2014.11.016
    139. Zhao, W., Chen, Z., Yang, X., Sheng, L., Mao, H., & Zhu, S. (2023). Metagenomics reveal arbuscular mycorrhizal fungi altering functional gene expression of rhizosphere microbial community to enhance Iris tectorum’s resistance to Cr stress. Science of the Total Environment, 895, 164970. https://doi.org/10.1016/j.scitotenv.2023.164970
    140. Zhao, Y., & Naeth, M. A. (2022). Soil amendment with a humic substance and arbuscular mycorrhizal fungi enhance coal mine reclamation. Science of the Total Environment, 823, 153696. https://doi.org/10.1016/j.scitotenv.2022.153696
    141. Zhu, B., Gao, T., Zhang, D., Fing, K., Li, C., & Ma, F. (2022). Functions of arbuscular mycorrhizal fungi in horticultural crops. Scientia Horticulturae, 303, 111219. https://doi.org/10.1016/j.scienta.2022.111219
    142. Zhu, Q., Xu, P., Lei, L., & Jing, Y. (2022). Transcriptome analysis reveals decreased accumulation and toxicity of Cd in upland rice inoculated with arbuscular mycorrhizal fungi. Applied Soil Ecology, 177, 104501. https://doi.org/10.1016/j.apsoil.2022.104501

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Copyright (c) 2025 The Authors

How to cite

Prisa, D., & Jamal, A. (2025). Sustainable approaches in modern agriculture: The role of arbuscular mycorrhizal fungi. Multidisciplinary Reviews, 8(7), 2025245. https://doi.org/10.31893/multirev.2025245
  • Article viewed - 950
  • PDF downloaded - 608