Allelopathic effect of Rapistrum rugosum L. weed on growth, physiological and biochemical parameters of Hibiscus sabdariffa L.

Document Type : Original research paper

Authors
Department of Plant Production, Faculty of Agriculture and Natural Resources, Gonbad Kavous University
Abstract
To study the allelopathic effect of decomposed fresh aerial parts of Rapistrum rugosum on growth, physiological and biochemical traits of Hibiscus sabdariffa, a pot experiment was conducted as a completely randomized design with three replications under greenhouse condition at the Gonbad Kavous University. Treatments were different amounts of R. rugosum residues (0, 10, 20, 40, 80, and 160 g kg-1 soil). The results showed that increasing the amount of R. rugosum residues significantly reduced the growth traits of H. sabdariffa. The lowest amount of stem and root length, fresh and dry weight of the plant was observed in 160 g kg-1 of R. rugosum residues. The content of chlorophyll b and carotenoids, as well as malondialdehyde, decreased with increasing the amount of R. rugosum. However, the trend of changes in the content of catalase enzyme, soluble sugars content, proline, total phenol, and flavonoids increased with increasing the amount of R. rugosum residues. Consequently, our findings showed that with the increasing in the amount of R. rugosum residues, all the studied traits of H. sabdariffa decreased significantly. Therefore, it can be recommended to use H. sabdariffa weed as a natural herbicide in sustainable agriculture especially in medicinal plant production.
Keywords
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Aebi, H. (1984). "[13] Catalase in vitro," in Methods in enzymology. Elsevier, 121-126.
Al-Watban, A., and Salama, H.M. (2012). Physiological effects of allelopathic activity of Artemisia monosperma on common bean (Phaseolus vulgaris L.). Int Res J Plant Sci 3(8): 158-163.
Arnon, D.I. (1949). Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiol 24(1): 1.
Asgharipour, M.R., and Armin, M. (2010). Inhibitory effects of Sorghum halepens root and leaf extracts on germination and early seedling growth of widely used medicinal plants. Adv Environ Biol: 316-325.
Baghestani, M.A., Najafi, H., and Zand, E. (2005). Wild mustard biology and management. Iranian Research Institute of Plant Protection press (In Persian with English summary).
Bais, H.P., Vepachedu, R., Gilroy, S., Callaway, R.M., and Vivanco, J.M. (2003). Allelopathy and exotic plant invasion: from molecules and genes to species interactions. Science 301(5638): 1377-1380.
Bates, L.S., Waldren, R.a., and Teare, I. (1973). Rapid determination of free proline for water-stress studies. Plant Soil 39: 205-207.
Bhadoria, P. (2010). Allelopathy: a natural way towards weed management. Am j exp agric 1(1): 7-20.
Chang, C.-C., Yang, M.-H., Wen, H.-M., and Chern, J.-C. (2002). Estimation of total flavonoid content in propolis by two complementary colorimetric methods. J Food Drug Anal 10(3).
Cipollini, D. (2016). A review of garlic mustard (Alliaria petiolata, Brassicaceae) as an allelopathic plant. J Torrey Bot Soc 143(4): 339-348.
Cruz‐Ortega, R., Ayala‐Cordero, G., and Anaya, A.L. (2002). Allelochemical stress produced by the aqueous leachate of Callicarpa acuminata: effects on roots of bean, maize, and tomato. Physiol Plant 116(1): 20-27.
Da-Costa-Rocha, I., Bonnlaender, B., Sievers, H., Pischel, I., and Heinrich, M. (2014). Hibiscus sabdariffa L.–A phytochemical and pharmacological review. Food Chem 165: 424-443.
Elisante, F., Tarimo, M.T., and Ndakidemi, P.A. (2013). Allelopathic effect of seed and leaf aqueous extracts of Datura stramonium on leaf chlorophyll content, shoot and root elongation of Cenchrus ciliaris and Neonotonia wightii. Am J Plant Sci 2013.
Farooq, M., Jabran, K., Cheema, Z.A., Wahid, A., and Siddique, K.H. (2011). The role of allelopathy in agricultural pest management. Pest Manag Sci 67(5): 493-506.
Feizi, H., Salari, A., and Gharar, F. (2018). Study of the allelopathic effect of saffron (Crocus sativus L.) organs’ aqueous extract on the seed germination and seedling growth of su-gar beet and safflower at different concentrations. J Herbs Spices Med Plants 22(4): 156-161.
Ghahreman, A. (1993). Plant systematics: cormophytes of Iran. Iran University Press 720p.
Gniazdowska, A., and Bogatek, R. (2005). Allelopathic interactions between plants. Multi site action of allelochemicals. Acta Physiol Plant 27: 395-407.
Gulzar, A., Siddiqui, M., and Bi, S. (2016). Phenolic acid allelochemicals induced morphological, ultrastructural, and cytological modification on Cassia sophera L. and Allium cepa L. Protoplasma 253: 1211-1221.
Han, C.-M., Pan, K.-W., Wu, N., Wang, J.-C., and Li, W. (2008). Allelopathic effect of ginger on seed germination and seedling growth of soybean and chive. Sci Hortic 116(3): 330-336.
Heath, R.L., and Packer, L. (1968). Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125(1): 189-198.
Hegab, M.M., and Ghareib, H.R. (2010). Antioxidative effects of acetone fraction and vanillic acid from Chenopodium murale L. on tomato plant. Weed Biol Manag 10: 64-72.
Hemeda, H., and Klein, B. (1990). Effects of naturally occurring antioxidants on peroxidase activity of vegetable extracts. J Food Sci 55(1): 184-185.
Jabran, K. (2017). "Manipulation of allelopathic crops for weed control." Springer, 66-75.
Jabran, K., Mahajan, G., Sardana, V., and Chauhan, B.S. (2015). Allelopathy for weed control in agricultural systems. Crop Protection 72: 57-65.
John, J., and Sarada, S. (2012). Role of phenolics in allelopathic interactions. Allelopathy J 29(2).
Kala, S. (2015). Effect of Nacl salt stress on antioxidant enzymes of isabgol (Plantago ovata Forsk.) genotypes. Int J Food Sci Tech Res 4: 40-43.
Khanh, T.D., Cong, L.C., Xuan, T.D., Lee, S.J., Kong, D.S., and Chung, I.M. (2008). Weed-suppressing potential of dodder (Cuscuta hygrophilae) and its phytotoxic constituents. Weed Sci 56(1): 119-127.
Kochert, G. (1978). Carbohydrate determination by the phenol-sulfuric acid method. In: Handbook of phycological methods, Physiological and biochemical methods.: 95.
Liu, D.L., An, M., Johnson, I.R., and Lovett, J.V. (2003). Mathematical modeling of allelopathy. III. A model for curve-fitting allelochemical dose responses. Nonlinearity in biology, toxicology, medicine 1(1): 15401420390844456.
Malik, C.P., and Singh, M. (1980). Plant enzymology and histo-enzymology. Kalyani Publishers, New Delhi, p 286.
Otusanya, O., Ogunwole, A., and Tijani, M. (2015). Allelopathic effect of Tithonia diversifolia and Chromolaena odorata on the germination, growth and chlorophyll accumulation of Hibiscus sabdariffa (L.). Int j botany res 5(3): 1-14.
Poornamazi, A.R., Gholamalipour, A.E., BIABANI, A., and Taliei, F. (2019). Evaluation of the allelopathic potential of some weeds on germination characteristics and photosynthetic pigments of cress seedlings (Lepidium sativum). Iran J Seed Res 6(1): 129-143.
Rahimzadeh, F., Tobeh, A., and Jamaati-e-Somarin, S. (2012). Study of allelopathic effects of aqueous extracts of roots and seeds of goosefoot, red-root amaranth and field bindweed on germination and growth of lentil seedlings. Int J Agron 3(9): 318-326.
Tigre, R., Silva, N., Santos, M., Honda, N., Falcao, E., and Pereira, E. (2012). Allelopathic and bioherbicidal potential of Cladonia verticillaris on the germination and growth of Lactuca sativa. Ecotoxicol Environ Saf 84: 125-132.
Wang, X., Wang, J., Zhang, R., Huang, Y., Feng, S., Ma, X., Zhang, Y., Sikdar, A., and Roy, R. (2018). Allelopathic effects of aqueous leaf extracts from four shrub species on seed germination and initial growth of Amygdalus pedunculata Pall. Forests 9(11): 711.
Volume 11, Issue 2
December 2023
Pages 55-65

  • Receive Date 06 January 2024
  • Revise Date 11 February 2024
  • Accept Date 20 February 2024
  • First Publish Date 20 February 2024