Research Article
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Year 2021, Volume: 4 Issue: 2, 61 - 66, 08.12.2021
https://doi.org/10.54565/jphcfum.1004433

Abstract

Supporting Institution

Fırat Üniversitesi

Project Number

FF.21.01

Thanks

Fübap, Fırat üniversitesi bitki doku kültürü laboratuvarı ve Sakarya mısır araştırma enstitüsüne gerekli olan desteklerinden dolayı teşekkür ederim.

References

  • [1] J. Derr, Plant Injury From Herbicide Residue, Virginia Cooperative Extension, Virginia Tech., Virginia State University, 2016.
  • [2] Ç. Mengüç, Herbicide Toxicity and Alternative Control Strategies Against Weeds, Turkish Journal of Weed Science, 2018, 21 (1): 61-73).
  • [3] L. de Freitas-Silva, M. Rodríguez-Ruiz, H. Houmani, L. C. da Silva, J. M. Palma and F. J. Corpas, Glyphosate-induced oxidative stress in Arabidopsis thaliana affecting peroxisomal metabolism and triggers activity in the oxidative phase of the pentose phosphate pathway (OxPPP) involved in NADPH generation, Journal of plant physiology, 2017, 218, 196-205.
  • [4] S. Yılmaz Sarıaltın and T. Çoban, Use of glyphosate and glyphosate-based herbicides risks for human health. Turkey Clinics J Pharm Sci 2017; 2016, 6 (1): 1-14.
  • [5] M. Basantani, A. Srivastava and S. Sen, Elevated antioxidant response and induction of tau-class glutathione S-transferase after glyphosate treatment in Vigna radiata (L.) Wilczek, Pesticide biochemistry and physiology, 2011, 99(1), 111-117.
  • [6] H. Torun, Investigation and mapping of the effect of crop rotation on herbicide resistance of infertile wild oat (Avena sterilis L.) in Osmaniye Province, PhD Thesis, Çukurova University, Institute of Science, 2017, Adana.
  • [7] I. Tepe, weeds and struggling with problems in the areas of agriculture and non-agriculture in Turkey, Yuzuncuyıl University, Faculty of Agriculture Publications, No: 18, 1997.
  • [8] D. Isik, H. Mennan, B. Bukun, A. Oz and M. Ngouajio, The Critical Period for Weed Control in Corn in Turkey, Weed technology, 2006, 20 (4), 867-872.
  • [9] N. Birışık, Chemical control from theory to practice, General Directorate of Food and Control. 1st Edition, Matsa printing house, 2018, Ankara.
  • [10] C. Soares, R. Pereira, S. Spormann and F. Fidalgo, “Is soil contamination by aglyphosate commercial formulation truly harmless to non-target plants? - Evaluation of oxidative damage and antioxidant responses in tomato”, Environmental Pollution, 2019, 247, 256-265.
  • [11] A. da Rosa Ulguim, D. Agostinetto, C. de Oliveira, Q. Ruchel, J. D. G. da Silva, L. Vargas and L. A. Avila, Does competition between soybeans and Wild Poinsettia with low-level resistance or susceptibility to glyphosate affect physiology and secondary metabolism ?. Semina: Ciências Agrárias, 2017, 38 (3), 1133-1144.
  • [12] F. H. Witham, D. F. Blaydes and R. M. Dewlin, “Experiments in Plant Physiology New York”. Von Nonstrand Reinhold Company, 1971, 55-56.
  • [13] G. Mourente, D. R. Tocher, E. Diaz, A. Grau and E. Pastor, "Relationships between antioxidants, antioxidant enzyme activities and lipid peroxidation products during early development in Dentex dentex eggs and larvae", Aquaculture, 1999, 179, 309–324.
  • [14] H. Aebi, “Catalase in Vitro, Method Enzym”, 1984, 105, 121-126.
  • [15] J.G. Bell, C.B. Cowey, J.W. Adron and A. M. Shanks, “Some effects of vitamin E and selenium deprivation on tissue enzyme levels and indices of tissue peroxidation in rainbow trout (Salmo gairdneri)”, British Journal of Nutrition, 1985, 53: 149–157.
  • [16] M. P. Gomes, S. G. Le Manac'h, S. Maccario, M. Labrecque, M. Lucotte and P. Juneau, Differential effects of glyphosate and aminomethylphosphonic acid (AMPA) on photosynthesis and chlorophyll metabolism in willow plants. Pesticide biochemistry and physiology, 2016, 130, 65-70. [17] G. C. Percival, The influence of glyphosate on carotenoid pigments, reactive oxygen species scavenging enzymes and secondary stress metabolites within leaf tissue of three Acer species, Urban forestry & urban greening, 2017, 24, 19-25.
  • [18] H. Singh, N. B. Singh, A. Singh, I. Hussain and V. Yadav, "Physiological and Biochemical Roles of Nitric Oxide Against Toxicity Produced by Glyphosate Herbicide in Pisum sativum", Russian Journal of Plant Physiology, 2017, 64, 4, 518–524.
  • [19] N. T. Harre, H. Nie, Y. Jiang and B. G. Young, Differential antioxidant enzyme activity in rapid ‐ response glyphosate resistant Ambrosia trifida, Pest management science, 2018, 74 (9), 2125-2132.
  • [20] B. Feng, H. Yu, Y. Hu, X. Gao, J. Gao, D. Gao, S. Zhang, The physiological characteristics of the low canopy temperature wheat (Triticum aestivum l.) genotypes under simulated drought condition, Acta Physiol Plant, 2009, 31:1229–1235.
  • [21] Y. Chang, J. Zhang, G. Bao, B. Yan, Y. Qu, M. Zhang and W. Tang, Physiological Responses of Highland Barley Seedlings to NaCl, Drought and Freeze-Thaw Stress, Journal of Plant Growth Regulation, 2020, 1-8.
  • [22] S. M. da Silva Lobato, L. R. dos Santos, B. R. S. da Silva, W. de Oliveira Melo and A. K. da Silva Lobato, Protective Mechanism Triggered by Pigeonpea Plants Exposed to Water Deficit: Modifications Linked to Paraheliotropism, Stomatal Characteristics and Antioxidant Enzymes, Journal of Plant Growth Regulation, 2020, 1-17.
  • [23] N. Liu, G. Zhong, J. Zhou, Y. Liu, Y. Pang, H. Cai and Z. Wu, Separate and combined effects of glyphosate and copper on growth and antioxidative enzymes in Salvinia natans (L.) All, Science of the Total Environment, 2019, 655, 1448-1456.
  • [24] D. E. M. Radwan and K. A. Fayez, Photosynthesis, antioxidant status and gas-exchange are altered by glyphosate application in peanut leaves, Photosynthetica, 2016, 54 (2): 307-316.
  • [25] D. Agostinetto, C. Oliveira, A. C. Langaro, M. A. Nohatto, ve R. Manica-Berto, Change in physiological features in ryegrass biotypes in competition with soybean due resistance to glyphosate, Planta Daninha, 2016, 34(3), 517-526.
  • [26] M. P. Gomes, E. M. Bicalho, E. Smedbol, F. V. D. S. Cruz, M. Lucotte and Q. S. Garcia, Glyphosate can decrease germination of glyphosate-resistant soybeans, Journal of agricultural and food chemistry, 2017, 65 (11), 2279-2286.
  • [27] G. Zhong, Z. Wu, N. Liu and J. Yin, Phosphate alleviation of glyphosate-induced toxicity in Hydrocharis dubia (Bl.) Backer, Aquatic Toxicology, 2018, 201, 91-98.
  • [28] I. G. Sergiev, V. S. Alexieva, S. V. Ivanov, I. I. Moscow and E. N. Karanov, The phenylurea cytokinin 4PU-30 protects maize plants against glyphosate action, Pesticide Biochemistry and Physiology, 2006, 85 (3), 139-146.
  • [29] G. Akbulut Beker, E. Yigit and D. Bayram, Effect of Glyphosate on Some Protective Systems in Zea mays L., YYU J. AGR. SCI., 2018, 28(1): 27-35. [30] S. S. Gill and N. Tuteja, Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants, Plant physiology and biochemistry, 2010, 48 (12), 909-930.

Effects of Glyphosate Herbicide on Photosynthetic Pigments and Antioxidant Enzyme Activities in Corn (Zea mays L.) and Wheat (Triticum aestivum L.) Varieties

Year 2021, Volume: 4 Issue: 2, 61 - 66, 08.12.2021
https://doi.org/10.54565/jphcfum.1004433

Abstract

In this study, it was determined that phytotoxic levels of glyphosate herbicide that will be banned in Europe may be at on wheat and corn plants. Biochemical responses due to the toxic effect of glyphosate at different concentrations were determined in corn (Zea mays L. cv. Ada 523) and wheat (Tritucum aestivum L. cv. Halis) varieties. For wheat and corn varieties, 4 different doses (0, 100, 500 and 1000 μM) of the herbicide were applied to 1-week-old and 15-day-old plants. Hydroponic medium was used for all applications on plants.
According to the results obtained; the toxic effect created by glyphosate increased the destruction of pigment in the leaves and significant decreases were detected. While GST, SOD and CAT activities increased in all concentrations of 1-week-old plants treated with glyphosate, only GST activity decreased at 100 μM concentration of wheat leaf and corn root. SOD and CAT activities were increased in 15-day-old wheat and corn plants treated with glyphosate. Only SOD activity decreased in the root part of the maize plant. GST activity was increased in the roots and leaves of the maize plant, while it decreased in wheat leaves and roots at a concentration of 100 μM. As a result, glyphosate was found to be effective at very low concentrations in wheat and corn regardless of age. It was also revealed that 1-week-old corn and wheat crops inhibit more phytotoxic effects than these 15-day-old plants. In other words, young plants were found to be more resistant.

Project Number

FF.21.01

References

  • [1] J. Derr, Plant Injury From Herbicide Residue, Virginia Cooperative Extension, Virginia Tech., Virginia State University, 2016.
  • [2] Ç. Mengüç, Herbicide Toxicity and Alternative Control Strategies Against Weeds, Turkish Journal of Weed Science, 2018, 21 (1): 61-73).
  • [3] L. de Freitas-Silva, M. Rodríguez-Ruiz, H. Houmani, L. C. da Silva, J. M. Palma and F. J. Corpas, Glyphosate-induced oxidative stress in Arabidopsis thaliana affecting peroxisomal metabolism and triggers activity in the oxidative phase of the pentose phosphate pathway (OxPPP) involved in NADPH generation, Journal of plant physiology, 2017, 218, 196-205.
  • [4] S. Yılmaz Sarıaltın and T. Çoban, Use of glyphosate and glyphosate-based herbicides risks for human health. Turkey Clinics J Pharm Sci 2017; 2016, 6 (1): 1-14.
  • [5] M. Basantani, A. Srivastava and S. Sen, Elevated antioxidant response and induction of tau-class glutathione S-transferase after glyphosate treatment in Vigna radiata (L.) Wilczek, Pesticide biochemistry and physiology, 2011, 99(1), 111-117.
  • [6] H. Torun, Investigation and mapping of the effect of crop rotation on herbicide resistance of infertile wild oat (Avena sterilis L.) in Osmaniye Province, PhD Thesis, Çukurova University, Institute of Science, 2017, Adana.
  • [7] I. Tepe, weeds and struggling with problems in the areas of agriculture and non-agriculture in Turkey, Yuzuncuyıl University, Faculty of Agriculture Publications, No: 18, 1997.
  • [8] D. Isik, H. Mennan, B. Bukun, A. Oz and M. Ngouajio, The Critical Period for Weed Control in Corn in Turkey, Weed technology, 2006, 20 (4), 867-872.
  • [9] N. Birışık, Chemical control from theory to practice, General Directorate of Food and Control. 1st Edition, Matsa printing house, 2018, Ankara.
  • [10] C. Soares, R. Pereira, S. Spormann and F. Fidalgo, “Is soil contamination by aglyphosate commercial formulation truly harmless to non-target plants? - Evaluation of oxidative damage and antioxidant responses in tomato”, Environmental Pollution, 2019, 247, 256-265.
  • [11] A. da Rosa Ulguim, D. Agostinetto, C. de Oliveira, Q. Ruchel, J. D. G. da Silva, L. Vargas and L. A. Avila, Does competition between soybeans and Wild Poinsettia with low-level resistance or susceptibility to glyphosate affect physiology and secondary metabolism ?. Semina: Ciências Agrárias, 2017, 38 (3), 1133-1144.
  • [12] F. H. Witham, D. F. Blaydes and R. M. Dewlin, “Experiments in Plant Physiology New York”. Von Nonstrand Reinhold Company, 1971, 55-56.
  • [13] G. Mourente, D. R. Tocher, E. Diaz, A. Grau and E. Pastor, "Relationships between antioxidants, antioxidant enzyme activities and lipid peroxidation products during early development in Dentex dentex eggs and larvae", Aquaculture, 1999, 179, 309–324.
  • [14] H. Aebi, “Catalase in Vitro, Method Enzym”, 1984, 105, 121-126.
  • [15] J.G. Bell, C.B. Cowey, J.W. Adron and A. M. Shanks, “Some effects of vitamin E and selenium deprivation on tissue enzyme levels and indices of tissue peroxidation in rainbow trout (Salmo gairdneri)”, British Journal of Nutrition, 1985, 53: 149–157.
  • [16] M. P. Gomes, S. G. Le Manac'h, S. Maccario, M. Labrecque, M. Lucotte and P. Juneau, Differential effects of glyphosate and aminomethylphosphonic acid (AMPA) on photosynthesis and chlorophyll metabolism in willow plants. Pesticide biochemistry and physiology, 2016, 130, 65-70. [17] G. C. Percival, The influence of glyphosate on carotenoid pigments, reactive oxygen species scavenging enzymes and secondary stress metabolites within leaf tissue of three Acer species, Urban forestry & urban greening, 2017, 24, 19-25.
  • [18] H. Singh, N. B. Singh, A. Singh, I. Hussain and V. Yadav, "Physiological and Biochemical Roles of Nitric Oxide Against Toxicity Produced by Glyphosate Herbicide in Pisum sativum", Russian Journal of Plant Physiology, 2017, 64, 4, 518–524.
  • [19] N. T. Harre, H. Nie, Y. Jiang and B. G. Young, Differential antioxidant enzyme activity in rapid ‐ response glyphosate resistant Ambrosia trifida, Pest management science, 2018, 74 (9), 2125-2132.
  • [20] B. Feng, H. Yu, Y. Hu, X. Gao, J. Gao, D. Gao, S. Zhang, The physiological characteristics of the low canopy temperature wheat (Triticum aestivum l.) genotypes under simulated drought condition, Acta Physiol Plant, 2009, 31:1229–1235.
  • [21] Y. Chang, J. Zhang, G. Bao, B. Yan, Y. Qu, M. Zhang and W. Tang, Physiological Responses of Highland Barley Seedlings to NaCl, Drought and Freeze-Thaw Stress, Journal of Plant Growth Regulation, 2020, 1-8.
  • [22] S. M. da Silva Lobato, L. R. dos Santos, B. R. S. da Silva, W. de Oliveira Melo and A. K. da Silva Lobato, Protective Mechanism Triggered by Pigeonpea Plants Exposed to Water Deficit: Modifications Linked to Paraheliotropism, Stomatal Characteristics and Antioxidant Enzymes, Journal of Plant Growth Regulation, 2020, 1-17.
  • [23] N. Liu, G. Zhong, J. Zhou, Y. Liu, Y. Pang, H. Cai and Z. Wu, Separate and combined effects of glyphosate and copper on growth and antioxidative enzymes in Salvinia natans (L.) All, Science of the Total Environment, 2019, 655, 1448-1456.
  • [24] D. E. M. Radwan and K. A. Fayez, Photosynthesis, antioxidant status and gas-exchange are altered by glyphosate application in peanut leaves, Photosynthetica, 2016, 54 (2): 307-316.
  • [25] D. Agostinetto, C. Oliveira, A. C. Langaro, M. A. Nohatto, ve R. Manica-Berto, Change in physiological features in ryegrass biotypes in competition with soybean due resistance to glyphosate, Planta Daninha, 2016, 34(3), 517-526.
  • [26] M. P. Gomes, E. M. Bicalho, E. Smedbol, F. V. D. S. Cruz, M. Lucotte and Q. S. Garcia, Glyphosate can decrease germination of glyphosate-resistant soybeans, Journal of agricultural and food chemistry, 2017, 65 (11), 2279-2286.
  • [27] G. Zhong, Z. Wu, N. Liu and J. Yin, Phosphate alleviation of glyphosate-induced toxicity in Hydrocharis dubia (Bl.) Backer, Aquatic Toxicology, 2018, 201, 91-98.
  • [28] I. G. Sergiev, V. S. Alexieva, S. V. Ivanov, I. I. Moscow and E. N. Karanov, The phenylurea cytokinin 4PU-30 protects maize plants against glyphosate action, Pesticide Biochemistry and Physiology, 2006, 85 (3), 139-146.
  • [29] G. Akbulut Beker, E. Yigit and D. Bayram, Effect of Glyphosate on Some Protective Systems in Zea mays L., YYU J. AGR. SCI., 2018, 28(1): 27-35. [30] S. S. Gill and N. Tuteja, Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants, Plant physiology and biochemistry, 2010, 48 (12), 909-930.
There are 28 citations in total.

Details

Primary Language English
Subjects Chemical Engineering
Journal Section Articles
Authors

Fadime Karabulut 0000-0001-5186-2303

Songül Çanakcı Gülengül 0000-0002-5731-6175

Project Number FF.21.01
Publication Date December 8, 2021
Submission Date October 5, 2021
Acceptance Date November 5, 2021
Published in Issue Year 2021 Volume: 4 Issue: 2

Cite

APA Karabulut, F., & Çanakcı Gülengül, S. (2021). Effects of Glyphosate Herbicide on Photosynthetic Pigments and Antioxidant Enzyme Activities in Corn (Zea mays L.) and Wheat (Triticum aestivum L.) Varieties. Journal of Physical Chemistry and Functional Materials, 4(2), 61-66. https://doi.org/10.54565/jphcfum.1004433
AMA Karabulut F, Çanakcı Gülengül S. Effects of Glyphosate Herbicide on Photosynthetic Pigments and Antioxidant Enzyme Activities in Corn (Zea mays L.) and Wheat (Triticum aestivum L.) Varieties. Journal of Physical Chemistry and Functional Materials. December 2021;4(2):61-66. doi:10.54565/jphcfum.1004433
Chicago Karabulut, Fadime, and Songül Çanakcı Gülengül. “Effects of Glyphosate Herbicide on Photosynthetic Pigments and Antioxidant Enzyme Activities in Corn (Zea Mays L.) and Wheat (Triticum Aestivum L.) Varieties”. Journal of Physical Chemistry and Functional Materials 4, no. 2 (December 2021): 61-66. https://doi.org/10.54565/jphcfum.1004433.
EndNote Karabulut F, Çanakcı Gülengül S (December 1, 2021) Effects of Glyphosate Herbicide on Photosynthetic Pigments and Antioxidant Enzyme Activities in Corn (Zea mays L.) and Wheat (Triticum aestivum L.) Varieties. Journal of Physical Chemistry and Functional Materials 4 2 61–66.
IEEE F. Karabulut and S. Çanakcı Gülengül, “Effects of Glyphosate Herbicide on Photosynthetic Pigments and Antioxidant Enzyme Activities in Corn (Zea mays L.) and Wheat (Triticum aestivum L.) Varieties”, Journal of Physical Chemistry and Functional Materials, vol. 4, no. 2, pp. 61–66, 2021, doi: 10.54565/jphcfum.1004433.
ISNAD Karabulut, Fadime - Çanakcı Gülengül, Songül. “Effects of Glyphosate Herbicide on Photosynthetic Pigments and Antioxidant Enzyme Activities in Corn (Zea Mays L.) and Wheat (Triticum Aestivum L.) Varieties”. Journal of Physical Chemistry and Functional Materials 4/2 (December 2021), 61-66. https://doi.org/10.54565/jphcfum.1004433.
JAMA Karabulut F, Çanakcı Gülengül S. Effects of Glyphosate Herbicide on Photosynthetic Pigments and Antioxidant Enzyme Activities in Corn (Zea mays L.) and Wheat (Triticum aestivum L.) Varieties. Journal of Physical Chemistry and Functional Materials. 2021;4:61–66.
MLA Karabulut, Fadime and Songül Çanakcı Gülengül. “Effects of Glyphosate Herbicide on Photosynthetic Pigments and Antioxidant Enzyme Activities in Corn (Zea Mays L.) and Wheat (Triticum Aestivum L.) Varieties”. Journal of Physical Chemistry and Functional Materials, vol. 4, no. 2, 2021, pp. 61-66, doi:10.54565/jphcfum.1004433.
Vancouver Karabulut F, Çanakcı Gülengül S. Effects of Glyphosate Herbicide on Photosynthetic Pigments and Antioxidant Enzyme Activities in Corn (Zea mays L.) and Wheat (Triticum aestivum L.) Varieties. Journal of Physical Chemistry and Functional Materials. 2021;4(2):61-6.