doi: 10.15389/agrobiology.2026.3.387eng
UDC: 631.81.095.337
Acknowledgements:
Supported financially by the Russian Science Foundation and the St. Petersburg State Autonomous Institution The Foundation for Support of Scientific, Scientific-Technical and Innovative Activities
GEOCHEMICAL ASPECTS OF IODINE AND ITS ROLE IN THE PLANT METABOLISM (review)
P.S. Filippova1, 2 ✉
1St. Petersburg Federal Research Center RAS, North-West Centre of Interdisciplinary Researches of Problems of Food Maintenance, 3, sh. Podbel’skogo. St. Petersburg—Pushkin, 196608 Russia;
2Agrophysical Research Institute, 14, Grazhdanskii prosp., St. Petersburg, 195220 Russia, e-mail tipolis@yandex.ru (✉ corresponding author)
ORCID:
Filippova P.S. orcid.org/0000-0001-9726-8844
Final revision received September 16, 2025
Accepted December 02, 2025
Iodine is an important element of the biosphere and is present in all living organisms. Iodine in the form of gas and water vapor is transferred to land, where it accumulates in soils mainly in the form of iodide (I-), iodate (IO3-), and organically bound iodine (S. Ahmad et al., 2021; S. Zhao et al., 2023; G. Jiang et al., 2024). Soil, in turn, serves as a source of iodine for groundwater (K. Yue et al., 2024). The spatial distribution of iodine in soils occurs through leaching, absorption by plants and soil organic matter, and evaporation (D.J. Ashworth, 2009). Aromatic compounds are the primary carriers of sedimentary iodine (S. Zhao et al., 2023). It is assumed that one of the most likely ways of iodine incorporation into soil organic matter is its binding to aromatic rings in the ortho- and para-position relative to the electron-donating group (amino group) of the aromatic ring (C. Xu et al., 2012). Many studies demonstrate that soil microorganisms are involved in the process of iodine transformation (Y. Muramatsu et al., 1999; C.M. Yeager et al., 2017; R.M. Grandbois et al., 2023). Iodine in soils is methylated and volatilized by oxidation of I- to CH3I, HIO, and I2 (S. Amachi et al., 2008; M. Seki et al., 2013). Extracellular bacterial enzymes play an important role in this process (Z. Jiang et al., 2024). It has been established that iodine is involved in many metabolic processes in plants (C. Kiferle et al., 2021; V.L. Nascimento et al., 2022; J.d.S. Lima et al., 2023). Iodine as a trace element enhances the activity of enzymes (N. Gupta et al., 2015; L.L. Rivera-Solís et al., 2025), increases the content of various antioxidants (B. Blasco et al., 2008; R. Leyva et al., 2011), accelerates the phenological phases (C. Kiferle et al., 2021), stimulates photosynthetic activity (R. Li et al., 2016; F. Mejía-Ramírez et al., 2023) and accumulation of nitrogen compounds (S. Smoleń et al., 2012), increases adaptivity in cases of abiotic stress (N. Gupta et al., 2015; J.D.S. Lima et al., 2023). In addition, plant analogues of thyroid hormones, such as triiodothyronine and tetraiodothyronine, have been discovered (L. Fowden, 1959; M.I. Garipova et al., 2020; S. Smoleń et al., 2023). In lettuce plants, iodine was present in the form of iodide (16.1 μg/L) and sodium salt of triiodothyronine (T3-Na) (484.1 μg/L) (S. Smoleń et al., 2021). It has been established that iodine is incorporated into peptides. Iodine is mostly incorporated into the tyrosine and histidine molecules in the amino acid sequences. Iodine affects the expression of various genes and the structure of proteins through iodination (C. Kiferle et al., 2021). The incorporation of iodine into organic substances such as proteins and enzymes highlights the importance of this trace element for plant development. Studying the biophilic nature of iodine and its affinity for organic compounds provides insights into the potential applications of iodine fertilizers.
Keywords: iodine, trace element, iodine geochemistry, plant metabolism, tyrosine, protein iodination.
REFERENCES
- Vinogradov A.P. Vvedenie v geokhimiyu okeana [Introduction to ocean geochemistry]. Moscow, 1967 (in Russ.).
- Dobrovol’skiy V.V. Osnovi biogeokhimii [Fundamentals of biogeochemistry]. Moscow, 1998 (in Russ.).
- Moreda-Piñeiro A., Romarís-Hortas V., Bermejo-Barrera P. A review on iodine speciation for environmental, biological and nutrition fields. Journal of Analytical Atomic Spectrometry, 2011, 26(11): 2107 CrossRef
- Whitehead D.C. The distribution and transformations of iodine in the environment. Environment International, 1984, 10: 321-339.
- Fuge R., Johnson C.C. The geochemistry of iodine — a review. Environmental Geochemistry and Health, 1986, 8: 31-54 CrossRef
- Carpenter L.J., Sturges W.T., Penkett S.A., Liss P.S., Alicke B., Hebestreit K., Platt U. Short-lived alkyl iodides and bromides at Mace Head, Ireland: Links to biogenic sources and halogen oxide production. Journal of Geophysical Research, 1999, 104(D1): 1679-1689 CrossRef
- Yuita K. Dynamics of iodine, bromine, and chlorine in soil: 2. Chemical forms of iodine in soil solutions. Soil Science and Plant Nutrition, 1992, 38(2): 281-287 CrossRef
- Yamada H., Kiriyama T., Onagawa Y., Hisamori I., Miyazaki C., Yonebayashi K. Speciation of iodine in soils. Soil Science and Plant Nutrition, 1999, 45(3): 563-568 CrossRef
- Yamada H., Hisamori I., Yonebayashi K. Identification of organically bound iodine in soil humic substances by size exclusion chromatography/inductively coupled plasma mass spectrometry (SEC/ICP-MS). Soil Science and Plant Nutrition, 2002, 48(3): 379-385 CrossRef
- Bowley H.E. Iodine dynamics in the terrestrial environment. PhD thesis. University of Nottingham, 2013.
- Roulier M., Bueno M., Thiry Y., Coppin F., Redon P.O., Le Hécho I., Pannier F. Iodine distribution and cycling in a beech (Fagus sylvatica) temperate forest. Science of the Total Environment, 2018, 645: 431-440 CrossRef
- Gonzali S., Kiferle C., Perata P. Iodine biofortification of crops: agronomic biofortification, metabolic engineering and iodine bioavailability. Current Opinion in Biotechnology, 2017, 44: 16-26 CrossRef
- Duborská E., Urík M., Šeda M. Iodine biofortification of vegetables could improve iodine supplementation status. Agronomy, 2020, 10(10): 1574 CrossRef
- Zhang Y., Cao H., Wang M., Zou Z., Zhou P., Wang X., Jin J. A review of iodine in plants with biofortification: uptake, accumulation, transportation, function, and toxicity. The Science of the Total Environment, 2023, 878: 163203 CrossRef
- Krzemińska J., Kapusta-Duch J., Smoleń S., Kowalska I., Słupski J., Skoczeń-Słupska R., Krawczyk K., Waśniowska J., Koronowicz A. Iodine enriched kale (Brassica oleracea var. sabellica L.) — The influence of heat treatments on its iodine content, basic composition and antioxidative properties. PLoS ONE, 2024, 19(6): e0304005 CrossRef
- Oztekin Y., Buyuktuncer Z. Agronomic biofortification of plants with iodine and selenium: a potential solution for iodine and selenium deficiencies. Biological Trace Element Research, 2025, 203(5): 2899-2910 CrossRef
- Eslamiparvar A., Hosseinifarahi M., Amiri S., Radi M. Combined bio fortification of spinach plant through foliar spraying with iodine and selenium elements. Scientific Reports, 2025, 15(1): 6722 CrossRef
- Somma A., Palmitessa O.D., Conversa G., Serio F., Santamaria P. Localized foliar application of iodine on tomato: an effective approach for targeted agronomic biofortification. Scientia Horticulturae, 2024, 327: 112807 CrossRef
- Lyons G.H. Biofortification of cereals with foliar selenium and iodine could reduce hypothyroidism. Frontiers in Plant Science, 2018, 9: 730 CrossRef
- Ikram N.A., Ghaffar A., Khan A.A., Nawaz F., Hussain A. Foliar iodine application: a strategy for tomato biofortification and yield optimization. Journal of Plant Nutrition, 2024, 48(1): 1-17 CrossRef
- Funahashi H., Imai T., Mase T., Sekiya M., Yokoi K., Hayashi H., Shibata A., Hayashi T., Nishikawa M., Suda N., Hibi Y., Mizuno Y., Tsukamura K., Hayakawa A., Tanuma S. Seaweed prevents breast cancer? Japanese Journal of Cancer Research, 2001, 92(5): 483-487 CrossRef
- Weng H.X., Hong C.L., Yan A.L., Pan L.H., Qin Y.C., Bao L.T., Xie L.L. Mechanism of iodine uptake by cabbage: effects of iodine species and where it is stored. Biological Trace Element Research, 2008, 125: 59-71 CrossRef
- Katagiri R., Asakura K., Uechi K., Masayasu S., Sasaki S. Adequacy of iodine intake in three different Japanese adult dietary patterns: a nationwide study. Nutrition Journal,2015, 14(1): 129 CrossRef
- Koronowicz A., Kopeć A., Master A., Smoleń S., Piątkowska E., Bieżanowska-Kopeć R., Ledwoyżw-Smoleń I., Skoczylas Ł., Rakoczy R., Leszczyńska T., Kapusta-Duch J., Pysz M. Transcriptome profiling of caco-2 cancer cell line following treatment with extracts from iodine biofortified lettuce (Lactuca sativa L.). PLoS ONE, 2016, 11(1): e0147336 CrossRef
- Li R., Li D.W., Yan A.L., Hong C.L., Liu H.P., Pan L.H., Song M.Y., Dai Z.X., Ye M.L., Weng H.X. The bioaccessibility of iodine in the biofortified vegetables throughout cooking and simulated digestion. Journal of Food Science and Technology, 2018, 55: 366-375 CrossRef
- Kashin V.K. Agrokhimiya, 1979, 11: 135-147 (in Russ.).
- Dai J.L., Zhu Y.G., Zhang M., Huang Y.Z. Selecting iodine-enriched vegetables and the residual effect of iodate application to soil. Biological Trace Element Research, 2004, 101(3): 265-276 CrossRef
- Sindireva A.V., Kurdumanova O.I., Stepanova O.V., Gilyazova I.B. Elektronniy nauchno-metodicheskiy zhurnal Omskogo GAU, 2016, 4(7): 1-6 (in Russ.).
- Stepanova O.V., Sindireva A.V., Shoykin O.D. Elektronniy nauchno-metodicheskiy zhurnal Omskogo GAU, 2017, 4(11) (in Russ.).
- Ivanov A.I., Filippova P.S., Filippov P.A. Agrokhimiya, 2021, 5: 37-46 CrossRef (in Russ.).
- Kiferle C., Martinelli M., Salzano A.M., Gonzali S., Beltrami S., Salvadori P.A., Hora K., Holwerda H.T., Scaloni A., Perata P. Evidences for a nutritional role of iodine in plants. Frontiers in Plant Science, 2021, 12: 616868 CrossRef
- Nascimento V.L., Souza B.C.O.Q., Lopes G., Guilherme L.R.G. On the role of iodine in plants: a commentary on benefits of this element. Frontiers in Plant Science, 2022, 13: 836835 CrossRef
- Lima J.d.S., Andrade O.V.S., Santos L.C.d., Morais E.G.d., Martins G.S., Mutz Y.S., Nascimento V.L., Marchiori P.E.R., Lopes G., Guilherme L.R.G. Soybean plants exposed to low concentrations of potassium iodide have better tolerance to water deficit through the antioxidant enzymatic system and photosynthesis modulation. Plants, 2023, 12(13): 2555 CrossRef
- Smoleń S., Czernicka M., Kęska-Izworska K., Kowalska I., Grzebelus D., Pitala J., Halka M., Skoczylas Ł., Tabaszewska M., Liszka-Skoczylas M., Grzanka M., Ledwożyw-Smoleń I., Koronowicz A., Krzemińska J., Sularz O., Kiełbasa D., Neupauer J., Kováčik P. Transcriptomic and metabolic studies on the role of inorganic and organic iodine compounds in lettuce plants. Scientific Reports, 2023, 13(1): 8440 CrossRef
- Vazhenin I.G., Belyakova V.I. Mikroelementi v zhizni rasteniy i zhivotnikh [Microelements in the life of plants and animals]. Moscow, 1952 (in Russ.).
- Gupta N., Bajpai M., Majumdar R., Mishra P. Response of iodine on antioxidant levels of Glycine max L. grown under Cd2+ stress. Advances in Biological Research, 2015, 9(1): 40-48.
- Rivera-Solís L.L., Ortega-Ortiz H., Benavides-Mendoza A., Flores-López M.L., Robledo-Olivo A., González-Morales S. Tomato biostimulation with nanochitosan-iodine complexes: enhancing antioxidant metabolism. Plants, 2025, 14(5): 801 CrossRef
- Blasco B., Rios J.J., Cervilla L., Sánchez-Rodrigez E., Ruiz J., Romero L. Iodine biofortification and antioxidant capacity of lettuce: potential benefits for cultivation and human health. Annals of Applied Biology, 2008, 152(3): 289-299 CrossRef
- Leyva R., Sánchez-Rodríguez E., Ríos J.J., Rubio-Wilhelmi M.M., Romero L., Ruiz J.M., Blasco B. Beneficial effects of exogenous iodine in lettuce plants subjected to salinity stress. Plant Science, 2011, 181(2): 195-202 CrossRef
- Li R., Liu H.P., Hong C.L., Dai Z.X., Liu J.W., Zhou J., Hu C.Q., Weng H.X. Iodide and iodate effects on the growth and fruit quality of strawberry. Journal of the Science of Food and Agriculture, 2016, 97(1): 230-235 CrossRef
- Mejía-Ramírez F., Benavides-Mendoza A., González-Morales S., Juárez-Maldonado A., Lara-Viveros F.M., Morales-Díaz A.B., Morelos-Moreno Á. Seed priming based on iodine and selenium influences the nutraceutical compounds in tomato (Solanum lycopersicum L.) crop. Antioxidants, 2023, 12(6): 1265 CrossRef
- Smoleń S., Sady W. Influence of iodine form and application method on the effectiveness of iodine biofortification, nitrogen metabolism as well as the content of mineral nutrients and heavy metals in spinach plants (Spinacia oleracea L.). Scientia Horticulturae,2012, 143: 176-183 CrossRef
- Hora K., Holwerda H.T. Loss of yield or lower fruit quality due to iodine deficiency in tomato and sweet pepper crops under heat stress can be prevented by application of potassium nitrate with iodine. Acta Horticulturae, 2023, 1372: 251-258 CrossRef
- Aleksandrovskaya E.I. Pochvovedenie, 1979, 6: 150-152 (in Russ.).
- Kashin V.K. Biogeokhimiya, fitofiziologiya i agrokhimiya yoda [Biogeochemistry, phytophysiology and agrochemistry of iodine]. Leningrad, 1987 (in Russ.).
- Pisarek P., Bueno M., Thiry Y., Legout A., Gallard H., Le Hécho I. Influence of tree species on selenium and iodine partitioning in an experimental forest ecosystem. Science of the Total Environment, 2022, 809: 151174 CrossRef
- Ali J., Mohiuddin M., Wang X., Hussain Z., Irshad M., Zia M.H., Pervez R., Okla M.K., Ahmad S. Spatial variation in iodine content with relation to soil physicochemical properties in lower Himalayan region. Environmental Research, 2024, 251(1): 118569 CrossRef
- Xue J., Deng Y., Zhang Y., Du Y., Fu Q.L., Xu Y., Shi J., Wang Y. Hidden role of organic matter in the immobilization and transformation of iodine on Fe-OM associations. Environmental Science and Technology, 2024, 58(22): 9840-9849 CrossRef
- Zhao S., Li J., Xue X., Sun D., Liu W., Zhu C., Yang Y., Xie X. Molecular characteristics of natural organic matter in the groundwater system with geogenic iodine contamination in the Datong Basin, Northern China. Chemosphere, 2023, 333: 138834 CrossRef
- Jiang G., Su C., Liu H., Wang X., Jiang J., Li J. Mobilization and enrichment of geogenic iodine in a floodplain groundwater system: New insights from sources and characterization of dissolved organic matter. Science of the Total Environment, 2024, 956: 177299 CrossRef
- Ahmad S., Bailey E.H., Arshad M., Ahmed S., Watts M.J., Young S.D. Multiple geochemical factors may cause iodine and selenium deficiency in Gilgit-Baltistan, Pakistan. Environmental Geochemistry and Health, 2021, 43(11): 4493-4513 CrossRef
- Ligowe I.S., Bailey E.H., Young S.D., Ander E.L., Kabambe V., Chilimba A.D., Lark R.M., Nalivata P.C. Agronomic iodine biofortification of leafy vegetables grown in Vertisols, Oxisols and Alfisols. Environmental Geochemistry and Health, 2021, 43(1): 361-374 CrossRef
- Sheppard M.I., Hawkins J.L. Iodine and microbial interactions in an organic soil. Journal of Environmental Radioactivity, 1995, 29(2): 91-109 CrossRef
- Schwehr K.A., Santschi P.H., Kaplan D.I., Yeager C.M., Brinkmeyer R. Organo-iodine formation in soils and aquifer sediments at ambient concentrations. Environmental Science and Technology, 2009, 43(19): 7258-7264 CrossRef
- Xu C., Zhang S., Ho Y.-F., Miller E.J., Roberts K.A., Li H.-P., Schwehr K., Otosaka S., Kaplan D.I., Brinkmeyer R., Yeager C., Santschi P.H. Is soil natural organic matter a sink or source for mobile radioiodine (129I) at the Savannah River Site? Geochimica et Cosmochimica Acta, 2011, 75: 5717-5735 CrossRef
- Francois R. The influence of humic substances on the geochemistry of iodine in nearshore and hemipelagic marine sediments. Geochimica et Cosmochimica Acta, 1987, 51: 2417-2427 CrossRef
- Xu C., Zhong J.Y., Hatcher P.G., Zhang S., Li H.-P., Ho Y.-F., Schwehr K.A., Kaplan D.I., Roberts K.A., Brinkmeyer R., Yeager C.M., Santschi P.H. Molecular environment of stable iodine and radioiodine (129I) in natural organic matter: evidence inferred from NMR and binding experiments at environmentally relevant concentrations. Geochimica et Cosmochimica Acta, 2012, 97: 166-182 CrossRef
- Konarbaeva G.A., Demin V.V. Agrokhimiya, 2011, 8: 73-80 (in Russ.).
- Konarbaeva G.A., Smolentsev B.A. Agrokhimiya, 2018, 7: 85-96 (in Russ.).
- Kashin V.K. Khimiya v interesakh ustoychivogo razvitiya, 2008, 16(2): 173-182 (in Russ.).
- Berezkin V.Yu., Korobova E.M., Danilova V.N. Vestnik Moskovskogo universiteta. Seriya 5: Geografiya, 2023, 1: 3-15 CrossRef (in Russ.).
- Weng H.X., Weng J.K., Yan A.L., Hong C.L., Yong W.B., Qin Y.C. Increment of iodine content in vegetable plants by applying iodized fertilizer and the residual characteristics of iodine in soil. Biological Trace Element Research, 2008, 123(1-3): 218-228 CrossRef
- Sheppard M.I., Thibault D.H. Chemical behaviour of iodine in organic and mineral soils. Applied Geochemistry, 1992, 7(3): 265-272 CrossRef
- Emerson H.P., Qafoku N.P., Johnson C.D., Szecsody J.E., Doughman M.S., Mackley R.D., Kaplan D.I. A paradigm shift for evaluating natural attenuation of radioactive iodine in soils and sediments: species-specific mechanisms and pathways. Journal of Environmental Management, 2025, 374: 124101 CrossRef
- Ashworth D.J. Transfers of iodine in the soil — plant — air system: solid–liquid partitioning, migration, plant uptake and volatilization. In: Comprehensive handbook of iodine. Academic Press, 2009: 107-118 CrossRef
- Shimamoto Y.S., Takahashi Y., Terada Y. Formation of organic iodine supplied as iodide in a soil-water system in Chiba, Japan. Environmental Science and Technology,2011, 45(6): 2086-2092 CrossRef
- Yue K., Yang Y., Qian K., Li Y., Pan H., Li J., Xie X. Spatial distribution and hydrogeochemical processes of high iodine groundwater in the Hetao Basin, China. Science of the Total Environment, 2024, 953: 176116 CrossRef
- Humphrey O.S., Young S.D., Crout N.M., Bailey E.H., Ander E.L., Watts M.J. Short-term iodine dynamics in soil solution. Environmental Science and Technology, 2020, 54(3): 1443-1450 CrossRef
- Mohiuddin M., Hussain Z., Abbasi A., Ali J., Irshad M., Tariq M.A., Intisar A., Hina A., Zaman Q.U., Ng A.W. Sawdust amendment in agricultural and pasture soils can reduce iodine losses. Sustainability, 2022, 14(20): 13620 CrossRef
- Korobova E.M., Berezkin V.Yu., Kolmikova L.I., Korsakova N.V. Vestnik Rossiyskogo universiteta druzhbi narodov. Seriya: Ekologiya i bezopasnost’ zhiznedeyatel’nosti, 2013, 4: 60-67 (in Russ.).
- Konarbaeva G.A., Smolentsev B.A. Agrokhimiya, 2014, 2: 50-59 (in Russ.).
- Konarbaeva G.A., Yakimenko V.N. Vestnik Tomskogo gosudarstvennogo universiteta. Biologiya, 2012, 4(20): 21-35 (in Russ.).
- Sheudzhen A.Kh. Biogeokhimiya [Biogeochemistry]. Maykop, 2003 (in Russ.).
- Panasin V.I., Vikhman M.I., Chechulin D.S., Rimarenko D.A. Plodorodie, 2019, 1: 31-35 CrossRef (in Russ.).
- Zhukova L.A., Khodirevskaya N.N. Materialy Mezhdunarodnoy nauchno-prakticheskoy konferentsii «Nauka i innovatsii v sel’skom khozyaystve (26-28 yanvarya 2011 g.)» [Proc. Int. Conf. «Science and innovation in agriculture (26-28 January 2011)»]. Kursk, 2011: 15-17 (in Russ.).
- Malisheva E.V. Vestnik Kurskoy gosudarstvennoy sel’skokhozyaystvennoy akademii, 2021, 5: 46-53 (in Russ.).
- Dibirova A.P., Akhmedova Z.N., Ramazanova N.I., Khizroeva P.R. Pochvovedenie, 2005, 8: 968-973 (in Russ.).
- Kurdumanova O.I., Zharkikh L.A. Materialy I Vserossiiskoy mezhdistsiplinarnoy nauchnoy konferentsii «Poznanie i deyatel’nost’: ot proshlogo k nastoyashchemu (05 dekabrya 2019 g.)» [Proc. I Russian Conf. «Cognition and action: From past to present (December 5, 2019)»]. Omsk, 2019: 351-355 (in Russ.).
- Siso A.I., Il’in V.B. Problemi agrokhimii i ekologii, 2008, 2: 33-36 (in Russ.).
- Mal’gin M.A. Khimiya v interesakh ustoychivogo razvitiya, 2001, 9(4): 555-566 (in Russ.).
- Puzanov A.V. Prioritetnie mikroelementi (I, Se, Mn, Co, Cu, Zn, Hg) v nazemnikh ekosistemakh Tuvinskoy gornoy oblasti. Avtoreferat doktorskoy dissertatsii [Priority microelements (I, Se, Mn, Co, Cu, Zn, Hg) in terrestrial ecosystems of the Tuva mountain region. DSc Thesis]. Novosibirsk, 2005 (in Russ.).
- Yeager C.M., Amachi S., Grandbois R., Kaplan D.I., Xu C., Schwehr K.A., Santschi P.H. Microbial transformation of iodine: from radioisotopes to iodine deficiency. Advances in Applied Microbiology, 2017, 101: 83-136 CrossRef
- Duborská E., Vojtková H., Matulová M., Šeda M., Matúš P. Microbial involvement in iodine cycle: mechanisms and potential applications. Frontiers in Bioengineering and Biotechnology, 2023, 11 CrossRef
- Grandbois R.M., Santschi P.H., Xu C., Mitchell J.M., Kaplan D.I., Yeager C.M. Iodide uptake by forest soils is principally related to the activity of extracellular oxidases. Frontiers in Chemistry, 2023, 11: 1105641 CrossRef
- Behrens H. New insights into the chemical behavior of radioiodine in aquatic environments. Proc. Int. Symp. «Environmental migration of long-lived radionuclides». International Atomic Energy Agency, Vienna, Austria, 1982.
- Koch J.T., Rachar D.B., Kay B.D. Microbial participation in iodide removal from solution by organic soils. Canadian Journal of Soil Science, 1989, 69(1): 127-135 CrossRef
- Bors J., Martens R. The contribution of microbial biomass to the adsorption of radioiodide in soils. Journal of Environmental Radioactivity, 1992, 15(1): 35-49 CrossRef
- Muramatsu Y., Yoshida S. Effects of microorganisms on the fate of iodine in the soil environment. Geomicrobiology Journal, 1999, 16(1): 85-93 CrossRef
- Nihei R., Usami M., Taguchi T., Amachi S. Role of fungal laccase in iodide oxidation in soils. Journal of Environmental Radioactivity, 2018, 189, 127-134 CrossRef
- Jiang Z., Jiang Y., Hu Y., Dong Y., Shi L. The crucial and versatile roles of bacteria in global biogeochemical cycling of iodine. Geo-Bio Interfaces,2024, 1: e5 CrossRef
- Li H.P., Yeager C.M., Brinkmeyer R., Zhang S., Ho Y.F., Xu C., Jones W.L., Schwehr K.A., Otosaka S., Roberts K.A., Kaplan D.I., Santschi P.H. Bacterial production of organic acids enhances H2O2-dependent iodide oxidation. Environmental Science and Technology, 2012, 46(9): 4837-4844 CrossRef
- Sokolova T.A. Pochvovedenie, 2020, 5: 559-575 CrossRef (in Russ.).
- Korzanov V.S., Ketov A.A., Kukovyakina A.V. Vestnik Permskogo universiteta. Seriya: Khimiya, 2011, 2(2): 89-95 (in Russ.).
- Yamagami M., Yanai M. Effect of rice plant root TTC-reducing activity on the chemical form of iodine in cultivated soil solutions. Radiation Protection Dosimetry, 2022, 198(13-15): 1189-1195 CrossRef
- Köhler F., Riebe B., Scheinost A.C., König C., Hölzer A., Walther C. Sorption of iodine in soils: insight from selective sequential extractions and X-ray absorption spectroscopy. Environmental Science and Pollution Research, 2019, 26(23): 23850-23860 CrossRef
- Roulier M., Carasco L., Orjollet D., Bueno M., Pannier F., Le Hécho I., Nicolas M., Coppin F. Iodine distribution and volatilization in contrasting forms of forest humus during a laboratory incubation experiment. Journal of Environmental Radioactivity, 2022, 248: 106872 CrossRef
- Keppler F., Borchers R., Elsner P., Fahimi I., Pracht J., Schöler H.F. Formation of volatile iodinated alkanes in soil: results from laboratory studies. Chemosphere, 2003, 52(2): 477-483 CrossRef
- Seki M., Oikawa J., Taguchi T., Ohnuki T., Muramatsu Y., Sakamoto K., Amachi S. Laccase-catalyzed oxidation of iodide and formation of organically bound iodine in soils. Environmental Science and Technology, 2013, 47(1): 390-397 3-2026CrossRef
- Amachi S. Microbial contribution to global iodine cycling: volatilization, accumulation, reduction, oxidation, and sorption of iodine. Microbes and Environments, 2008, 23(4): 269-276 CrossRef
- Amachi S., Kasahara M., Hanada S., Kamagata Y., Shinoyama H., Fujii T., Muramatsu Y. Microbial participation in iodine volatilization from soils. Environmental Science and Technology, 2003, 37(17): 3885-3890 CrossRef
- Ban-nai T., Muramatsu Y., Amachi S. Rate of iodine volatilization and accumulation by filamentous fungi through laboratory cultures. Chemosphere, 2006, 65(11): 2216-2222 CrossRef
- Duborská E., Urík M., Bujdoš M., Kubová J. Aging and substrate type effects on iodide and iodate accumulation by barley (Hordeum vulgare L.). Water Air and Soil Pollution, 2016, 227(11): 407 CrossRef
- Duborská E., Urík M., Bujdoš M. Comparison of iodide and iodate accumulation and volatilization by filamentous fungi during static cultivation. Water, Air, and Soil Pollution, 2017, 228: 225 CrossRef
- Guo J., Jiang J., Peng Z., Zhong Y., Jiang Y., Jiang Z., Hu Y., Dong Y., Shi L. Global occurrence of the bacteria with capability for extracellular reduction of iodate. Frontiers in Microbiology, 2022, 13: 1070601 CrossRef
- Shin H.D., Toporek Y., Mok J.K., Maekawa R., Lee B.D., Howard M.H., DiChristina T.J. Iodate reduction by Shewanella oneidensis requires genes encoding an extracellular dimethylsulfoxide reductase. Frontiers in Microbiology, 2022, 13: 852942 CrossRef
- Humphrey O.S., Young S.D., Bailey E.H., Crout N.M.J., Ander E.L., Hamilton E.M., Watts M.J. Iodine uptake, storage and translocation mechanisms in spinach (Spinacia oleracea L.). Environmental Geochemistry and Health, 2019, 41(5): 2145-2156 CrossRef
- Dyląg A., Smoleń S., Wisła-Świder A., Kowalska I., Sularz O., Krzemińska J., Pitala J., Koronowicz A. Evaluation of the chemical composition and nutritional value of lettuce (Lactuca sativa L.) biofortified in hydroponics with iodine in the form of iodoquinolines. Frontiers in Plant Science, 2023, 14: 1288773 CrossRef
- Smoleń S., Kowalska I., Wisła-Świder A., Ledwożyw-Smoleń I., Pitala J., Kiełbasa D., Koronowicz A. Use of iodoquinolines for iodine biofortification of potato plants. Food Chemistry, 2025, 472: 142825 CrossRef
- Smoleń S., Kowalska I., Halka M., Ledwożyw-Smoleń I., Grzanka M., Skoczylas Ł., Czernicka M., Pitala J. Selected aspects of iodate and iodosalicylate metabolism in lettuce including the activity of vanadium dependent haloperoxidases as affected by exogenous vanadium. Agronomy, 2020, 10(1): 1 CrossRef
- Fowden L. Radioactive iodine incorporation into organic compounds of various angiosperms. Physiologia Plantarum, 1959, 12(4): 657-664 CrossRef
- Garipova M.I., Farkhutdinov R.G., Sotnikova Yu.M. Izvestiya VUZov. Prikladnaya khimiya i biotekhnologiya, 2020, 10(4): 639-645 CrossRef (in Russ.).
- Bol’shakova L.S., Lisitsin A.B., Chernukha I.M., Zubtsov Yu.N., Lukin D.E., Lyublinskiy S.L. Voprosi pitaniya, 2018, 87(3): 12-17 CrossRef (in Russ.).
- Schenck C.A., Maeda H.A. Tyrosine biosynthesis, metabolism, and catabolism in plants. Phytochemistry, 2018, 149: 82-102 CrossRef
- Garipova M.I., Fedyaev V.V., Datsko O.I. Izvestiya vuzov. Prikladnaya khimiya i biotekhnologiya, 2024, 14(2): 229-235 CrossRef (in Russ.).
- Sagatov K. Botanicheskiy zhurnal, 1963, 48(8): 1151-1160 (in Russ.).
- Portyanko V.F., Lizhenko I.I., Portyanko V.V. Fiziologiya rasteniy, 1969, 16(5): 885-889 (in Russ.).
- Smoleń S., Czernicka M., Kowalska I., Keska K., Halka M., Grzebelus D., Grzanka M., Skoczylas Ł., Pitala J., Koronowicz A., Kováčik P. New aspects of uptake and metabolism of non-organic and organic iodine compounds-the role of vanadium and plant-derived thyroid hormone analogs in lettuce. Frontiers in Plant Science, 2021, 12: 653168 CrossRef
- Sularz O., Smoleń S., Koronowicz A., Kowalska I., Leszczyńska T. Chemical composition of lettuce (Lactuca sativa l.) biofortified with iodine by KIO3, 5-iodo-, and 3,5-diiodosalicylic acid in a hydroponic cultivation. Agronomy, 2020, 10(7): 1022 CrossRef
- Kato S., Wachi T., Yoshihira K., Nakagawa T., Ishikawa A., Takagi D., Tezuka A., Yoshida H., Yoshida S., Sekimoto H., Takahashi M. Rice (Oryza sativa L.) roots have iodate reduction activity in response to iodine. Frontiers in Plant Science, 2013, 4: 227 CrossRef
- Dobosy P., Nguyen H.T.P., Záray G., Streli C., Ingerle D., Ziegler P., Radtke M., Buzanich A.G., Endrédi A., Fodor F. Effect of iodine species on biofortification of iodine in cabbage plants cultivated in hydroponic cultures. Scientific Reports, 2024, 14(1): 15794 CrossRef
- Mackowiak C.L., Grossl P.R. Iodate and iodide effects on iodine uptake and partitioning in rice (Oryza sativa L.) grown in solution culture. Plant and Soil, 1999, 212: 133-141 CrossRef
- Attieh J.M., Hanson A.D., Saini H.S. Purification and characterization of a novel methyltransferase responsible for biosynthesis of halomethanes and methanethiol in Brassica oleracea. Journal of Biological Chemistry, 1995, 270(16): 9250-9257 CrossRef
- Itoh N., Toda H., Matsuda M., Negishi T., Taniguchi T., Ohsawa N. Involvement of S-adenosylmethionine-dependent halide/thiol methyltransferase (HTMT) in methyl halide emissions from agricultural plants: isolation and characterization of an HTMT-coding gene from Raphanus sativus (Daikon radish). BMC Plant Biology, 2009, 9: 116 CrossRef
- Medrano-Macías J., Leija-Martínez P., González-Morales S., Juárez-Maldonado A., Benavides-Mendoza A. Use of iodine to biofortify and promote growth and stress tolerance in crops. Frontiers in Plant Science, 2016, 7: 1146 CrossRef
- Leblanc C., Colin C., Cosse A., Delage L., La Barre S., Morin P., Fiévet B., Voiseux C., Ambroise Y., Verhaeghe E., Amouroux D., Donard O., Tessier E., Potin P. Iodine transfers in the coastal marine environment: the key role of brown algae and of their vanadium-dependent haloperoxidases. Biochimie, 2006, 88(11): 1773-1785 CrossRef
- Landini M., Gonzali S., Kiferle C., Tonacchera M., Agretti P., Dimida A., Vitti P., Alpi A., Pinchera A., Perata P. Metabolic engineering of the iodine content in Arabidopsis. Scientific Reports, 2012, 2: 338 CrossRef
- Carlessi M., Mariotti L., Giaume F., Fornara F., Perata P., Gonzali S. Targeted knockout of the gene OsHOL1 removes methyliodide emissions from rice plants. Scientific Reports, 2021, 11: 17010 CrossRef
- Rhew R.C., Østergaard L., Saltzman E.S., Yanofsky M.F. Genetic control of methyl halide production in Arabidopsis. Current Biology, 2003, 13(20): 1809-1813 CrossRef
- Mageshen V.R., Santhy P., Meena S., Latha M.R., Senthil A., Saraswathi T.R., Janaki P. Residual effect of biofortified iodine in soil, plant, crop yield and quality of tomato (Solanum lycopersicum L.). Research on Crops, 2022, 23(4): 801-807 CrossRef
- Yanai M., Kawabata H., Takaku Y. Chemical form of volatilized iodine obtained from orchard grass (Dactylis glomerata L.). Radiation Protection Dosimetry, 2024, 200(16-18): 1738-1743 CrossRef
- Saini H.S., Attieh J.M., Hanson A.D. Biosynthesis of halomethanes and methanethiol by higher plants via a novel methyltransferase reaction. Plant, Cell and Environment, 1995, 18(9): 1027-1033 CrossRef
- Satoh Y., Ohtsuka Y. Investigation of changes in the iodine concentrations of oceanic sediment and terrestrial soil samples after thermal drying. Environmental Monitoring and Assessment, 2023, 195: 429 CrossRef
- Shalaby O.A. Iodine application induces the antioxidant defense system, alleviates salt stress, reduces nitrate content, and increases the nutritional value of lettuce plants. Functional Plant Biology, 2025, 52(6): FP24273 CrossRef
- Quispe A.P.V., de Morais E.G., Benevenute P.A.N., Lima J.d.S., dos Santos L.C., Silva M.A., Chalfun-Júnior A., Marchiori P.E.R., Guilherme L.R.G. Priming effect with selenium and iodine on broccoli seedlings: activation of biochemical mechanisms to mitigate cold damages. Plant Physiology and Biochemistry, 2025, 223: 109876 CrossRef
- Andrade O.V.S., Lima J.d.S., das Neves T.T., de Morais E.G., Benevenute P.A.N., dos Santos L.C., Nascimento V.L., Guilherme L.R.G., Marchiori P.E.R. The Role of potassium iodate in mitigating the damages of water deficit in coffee plants. Journal of Soil Science and Plant Nutrition, 2024, 24: 5772-5788 CrossRef
- Riyazuddin R., Singh K., Iqbal N., Nisha N., Rani A., Kumar M., Khatri N., Siddiqui M.H., Yasheshwar, Kim S.T., Attila F., Gupta R. Iodine: an emerging biostimulant of growth and stress responses in plants. Plant and Soil, 2023, 486: 119-133 CrossRef
- Huliaieva H., Tokovenko I., Kharchuk M., Bohdan M., Pasichnyk L. The influence of iodine nano citrates on juvenile wheat plants at phytopathogenic infection and cooling stress. Plant Nano Biology, 2025, 13: 100175 3-2026CrossRef
- Sun J., Jin J., Xia J., Yu R., Zhang Y., Hou J., Gao C., Wang M. Integration of phenotypic, accumulative, physiological-biochemical, and transcriptomic analyses reveals new insights in lettuce response to iodine: enhancement or toxic effects. Journal of Agricultural and Food Chemistry, 2025, 73(23): 14533-14547 CrossRef
- Smoleń S., Sady W., Ledwożyw-Smoleń I., Strzetelski P., Liszka-Skoczylas M., Rożek S. Quality of fresh and stored carrots depending on iodine and nitrogen fertilization. Food Chemistry, 2014, 159: 316-322 CrossRef
- Smoleń S., Wierzbińska J., Sady W., Kołton A., Wiszniewska A., Liszka-Skoczylas M. Iodine biofortification with additional application of salicylic acid affects yield and selected parameters of chemical composition of tomato fruits (Solanum lycopersicum L.). Scientia Horticulturae, 2015, 188: 89-96 CrossRef
- Smoleń S., Kowalska I., Kováčik P., Sady W., Grzanka M., Kutman U.B. Changes in the chemical composition of six lettuce cultivars (Lactuca sativa L.) in response to biofortification with iodine and selenium combined with salicylic acid application. Agronomy, 2019, 9(10): 660 CrossRef
- Ajiwe S.T., Popoola A.R., Afolabi C.G., Oduwaye O.A., Ganiyu S.A., Fajinmi O.B., Chikaleke V.A., Imonmion J.E., Adigun J.A., Taiwo B.F., Uzoemeka I.P. Effect of iodine biofortification on incidence and severity of Fusarium wilt and yield of tomato (Solanum lycopersicum L.). Nigerian Journal of Biotechnology, 2019, 36(1): 146-151 CrossRef
- Kalenska S., Falko G., Antal T., Hordyna O., Fediv R. Iodine-containing preparations in grain growing technologies. Plant and Soil Science, 2023, 14(2) CrossRef
- Yalpani N., Raskin I. Salicylic acid: a systemic signal in induced plant disease resistance. Trends in Microbiology, 1993, 1(3): 88-92 CrossRef
- Zhong Q., Hu H., Fan B., Zhu C., Chen Z. Biosynthesis and roles of salicylic acid in balancing stress response and growth in plants. International Journal of Molecular Sciences, 2021, 22(21): 11672 CrossRef












