The Allelopathic Effect of Two Barley Cultivars (Hordeum vulgare) on Growth and Physiological Attributes of Bindweed (Convolvulus arvensis) Rhizome

Document Type : Research Article

Authors

Department of Weed Science, Shoushtar Branch, Islamic Azad University, Shoushtar, Iran

Abstract

Introduction: Barley is known to be an allelopathic plant and its allelopathic potential on weeds, and some other crops has been proven. Increasing use of herbicides has an adverse environmental impact and increases the weed resistance to herbicides. Eco-friendly methods for controlling weeds reduce the amount of herbicide use and reduce the damage caused by it. Some plants have alternate properties (allelopathies) that can be used to reduce or stop the growth of other plants, especially weeds. Allelopathy is an interference mechanism based on any direct or indirect effect (primarily inhibitory) by one plant on another through the release of chemicals that escape into the environment. Barley (Hordeum vulgare L. ssp. vulgare) is well known for its allelopathic compounds. The decomposition of barley plant residues in the soil, release numerous allelochemical compounds such as phenolic compounds, flavonoids, synoglycosides, alkaloids and polyamines. Till now 44 chemicals have been identified as potential allelochemicals that contribute to its allelopathic activity in Hordeum vulgare. The present work aimed to study the allelopathy potentials expressed by residues as straw among two barley genotypes on rhizome growth and physiological attribute of bindweed (Convolvulus arvensis L.).
Materials and Methods: This experiment was conducted in 2013 at Islamic Azad University, Shoushtar Branch. The experiment was factorial based on completely randomized design (CRD) with four replications. Four different amounts (10, 20, 30 and 40 g per one kg soil) of two barley cultivars (local ecotype and Sarasary 10) residual were prepared. Rhizomes were harvested from a depth of 30 cm soil and cultivated in the pot. The culture medium included plastic pots of 30 cm in diameter. The traits included seedling weight and length, malondialdehyde concentration, fatty acid percent, α-amylase activity, catalase activity, peroxidase activity, glutathione reductase activity, GA and ABA concentration of bindweed rhizome. The concentration of GA and ABA hormones was investigated based on the Kamal method. Statistical analysis was made using the SPSS Ver.13 statistical program. Significantly different means were separated at the 0.05 probability level (p = 0.05) by the least significant difference (LSD) test. Pearson’s correlation analysis was also conducted among different variables.
Results and Discussion: Results indicated the effect of genotype, residual amount and their interaction on rhizome malondialdehyde concentration, fatty acid percent, α-amylase activity, catalase activity, peroxidase activity, Glutathione reductase activity, GA and ABA concentration. Increasing the amount of residues for the local genotype caused a significant decrease in seedling fresh weight. The lowest fresh weight of bindweed was 40 g residues of local genotypes, in which was 73.6% lower than the control without residues. Increasing the amount of local and Sarasary 10 residues in the soil caused a significant reduction in the length of the bindweed seedlings. The negative effect of local ecotype residual on α-amylase activity was more than modern genotype. The mixing of 40 g residues of local ecotype and Sarasary10 genotype with soil decreased this enzyme by 38% and 79.5%, respectively, compared to the control without residues. Increasing the amount of residuals, reduces gibberellin hormone and increased rhizome the ABA content. The slope of the changes in gibberellin hormone and the increase of ABA in the local ecotype was higher than the modern genotype. Antioxidant enzymes increased in response to an increase in the amount of residues up to about 20 grams in the pot and then decreased significantly. Reducing antioxidant enzymes at high levels of barley residues led to an increase in the amount of fatty acids and Malondialdehyde, indicating the peroxidation of the cell membrane. In general, the residuals of local genotype compared to cultivar Sarasary 10 had a more harmful effect on all studied traits of bindweed rhizome and seedling. It seems that in areas where bindweed is dominant, it is possible to use local barley residuals to reduce the damages.

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1-       Agrawl J., Sairam R.K., Srivasta G.C., Tyagi A., and Meena R.C. 2005. Role of ABA salisylic acid, calcium and hydrogen peroxide on antioxidant enzymes induction in wheat seedling. Planet Science 169: 559-570.
2-       Ashrafi Z.Y., Sadeghi S., Mashhadi H.R., and Alizade H.M. 2008. Study of allelopathical effects of barley on inhibition of germination and growth of seedling green foxtail. Journal of SAT Agricultural Research 6: 1-6.
3-       Ashrafi Z.Y., Sadeghi S., and Mashhadi H.R. 2009. Inhibitive effects of barley (Hordeum vulgare) on germination and growth of seedling quack grass (Agropyrum repens). Icelandic Agricultural Sciences 22: 37-43.
4-       Ben-Hammouda M., Oueslati O., and Habib M. 2001. Auto-Toxicity of barley residues in direct sowing. Laboratoire de Physiologie de la Production des Céréales, Tunisia. 1-9. (In Spanish with English abstract)
5-       Bertholdsson N.O. 2004. Variation in allelopathic activity over 100 years of barley selection and breeding. Weed Research 44: 78-86.
6-       Bogatek R., Gniazdowska A., Zakrzewska W., Oracz K., and Gawroski S.W. 2005. Allelopathic effects of sunflower extracts on mustard seed germination and seedling growth. Biology Plantarum 50: 156-158.
7-       Bouhaouel I., Gfeller A., Fauconnier M.L., Rezgui S., Amara H., and Jadin P. 2015. Allelopathic and autotoxicity effects of barley (Hordeum vulgare L. ssp. vulgare) root exudates. BioControl 60: 425-436.
8-       Chance B., and Maehly A.C. 1995. Assay of catalase and peroxidases. Methods Enzymology 2: 764-775.
9-       Chinnusamy V., Schumaker K., and Zhu J.K. 2004. Molecular genetic perspectives on cross-talk and specificity in abiotic stress signaling in plants. Journal of Experimental Botany 55: 225-236.
10-   Chon S.U., and Kim Y.M. 2004. Herbicidal potential and quantification of suspected allelochemicals from four grass crop extracts. Journal of Agronomy and Crop Science 190: 145-150.
11-   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. Physiologia Plantarum 116: 20–27.
12-   Dhima K.V., Vasilakoglou I.B., Eleftherohorinos I.G., and Lithourgidis A.S. 2006. Allelopathic potential of winter cereals and their cover crop mulch effect on grass weed suppression and corn development. Crop Science 46: 345-352.
13-   Ding H., Cheng Z., Liu M., Hayat S., and Feng H. 2016. Garlic exerts allelopathic effects on pepper physiology in a hydroponic co-culture system. Biology Open 5(5): 631–637.
14-   Farhoudi R., and Lee D. 2013. Allelopathic effects of barley extract (Hordeum vulgare) on sucrose synthase activity, lipid peroxidation and antioxidant enzymatic activities of Hordeum spontoneum and Avena ludoviciana. Proceeding National Academy of Science Indian Section, Biological Science 83(3): 447–452.
15-   Farhoudi R., and Makizadeh M. 2011. Allelopathic effect of barley aqueous extract on α-amylase activity and seedling growth of wild oat and ryegrass. 2nd conference of seed science and technology. Mashhad, Iran. (In Persian with English Abstract)  
16-    Farhoudi R., Modhej A., and Alavinia S.R. 2014. Effects of Allelopathic Compounds of Barley (Hordeum vulgare L.) on Seed Germination, Seedling Growth and Some Antioxidant Activities of Chenopodium album L. Journal of Plant Protection 28(2): 234-241. (In Persian with English Abstract)
17-   Farhoudi R., Koreshnejad N., and Modhej A. 2014. Effect of wheat aquatic extract (Triticum aestivum cv. Chamran) on germination, vegetative growth, cell membrane damage, a-amylase enzyme and sucrose synthesis enzymes activity of winter wild oat (Avena ludoviciana). Journal of Plant Protection 28(1): 147-150. (In Persian with English Abstract)
18-   Farhoudi R., Sohelifar A., and Modhej A. 2016. Effect of Globe Artichoke (Cynara cardunculus L. var. scolymus L. Fiori) aqueous extracts on antioxidant enzymes activites, endogenous phytohormones concentration and α-amylase activity of Johnson grass (Sorghum halepense) rhizomes at germination stage. Journal Plant Proc. Func 5(17): 75-82. (In Persian with English Abstract)
19-   Gfeller A., Laloux M., Barsics F., Kati D.E., Haubruge E., du Jardin P., Verheggen F.J., Lognay G., Wathelet J.P., and Fauconnier M.L. 2013. Characterization of volatile organic compounds emitted by barley (Hordeum vulgare L.) roots and their attractiveness to wireworms. Journal of Chememical Ecology 39: 1129-1139.
20-   Gniazdowska A., and Bogatek R. 2005. Allelopathic interactions between plants. Multisite Action of Allelochemicals 27(3): 395–407.
21-   Gubbels G.H., and Kenaschuk E.O. 1989. Agronomic performance of flax grown on canola, barley and flax stubble with and without tillage prior to seeding. Canadian Journal of Plant Science 69: 31-38.20.
22-   Jafarzadeh N. 2006. Allelopathic potential of barley. The first national conference of legumes. Mashhad. Iran. 29-30. (In Persian with English Abstract)
23-   Kamal J. 2011.Impact of allelopathy of sunflower (Helianthus annuus L.) roots extract on physiology of wheat (Triticum aestivum L.). African Journal of Biotechnology 10(65): 14465-14477.
24-   Kang G.Q., Wan F.H., Liu X., and Guo L. 2008. Influence of two allelochemicals from Ageratina adenophora Sprengel on ABA, IAA and ZR contents in roots of upland rice seedlings. Allelopathy Journal 21: 253-262.
25-   Kato-Noguchi H., and Macias F.A. 2008. Inhibition of germination and α-amylase induction by 6-methoxy-2-benzoxazolinone in twelve plant species. Biological Plantaum 52: 351-354.
26-   Kremer R.J., and Ben-Hammoud M. 2009. Allelopathic Plants. 19. Barley (Hordeum vulgare L.). Allelopathy Journal 24(2): 225-242.
27-   Lorenzo P., Palomera-Pe´rez A., Reigosa M.J., and Gonzal L. 2011. Allelopathic interference of invasive Acacia dealbata Link on the physiological parameters of native understory species. Plant Ecology 212: 403-411.
28-   Munns R. 2002. Comparative physiology of salt and water stress. Plant, Cell and Environment 25: 239-250.
29-   Oracz K., Bailly C., Gniazdowska A., Côme D., Corbineau D., and Bogatek R. 2007. Induction of oxidative stress by sunflower phytotoxins in germinating mustard seeds. Journal of Chemical Ecology 33: 251-264.
30-   Oueslati O., Ben-Hammouda M., Ghorbal M.H., Guezzah M., and Kremer R.J. 2005. Barley Autotoxicity as Influenced by Varietal and Seasonal Variation. Journal Agronomy and Crop Science 191: 249-254.
31-   Oveisi M., Hamid R., Mashhadi M., Baghestani H., Alizadeh M., and Badri S. 2008. Assessment of the allelopathic potential of 17 Iranian barley cultivars in different development stages and their variations over 60 years of selection. Weed Biology and Management 8: 225–232.
32-   Pushak S., Peterson D., and Stahlman P.W. 1999. Field bindweed control in field crops. New York. John Wiley and Sons, INC.
33-   Valentovic P., Luxova M., Kolarovi L., and Gasparikora O. 2006. Effect of osmotic stress on compatible solutes content, membrane stability and water relation in two maize cultivars. Plant, Soil and Environment 52(4): 186-191.
34-   Xiao Z., Storms R., and Tsang A. 2006. A quantitative starch-iodine method for measuring alpha-amylase and glucoamylase activities. Analual Biochemistry 351: 146-148.
35-   Zimdahl R.L. 2004. Weed crop competition. Blackwell Publication. Canada. P22.
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