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Physiological and biochemical responses of basil to some allelopathic plant residues and dodder infestation

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Abstract

In the present study, the effects of three allelopathic plant residues, namely Syrian bean-caper (Zygophyllum fabago L.), marigold (Calendula officinalis L.), and jimsonweed (Datura stramonium L.) on two cultivar of sweet basil (Ocimum basilicum L.) plants infested by dodder (Cuscuta campestris Yunck.) were examined using factorial experiment in randomized complete block design with three replications. Means comparison revealed that the degree of sensitivity to allelopathic plant residues and dodder infestation in Iranian cultivar (Mubarake) of the basil was more than that of the Italian cultivar. In the plants, infested by dodder, a significant increase in the content of total soluble sugars, peroxidase activity, catalase, superoxide dismutase, ascorbate peroxidase and the initial fluorescence (F0) was observed, while a noticeable decrease in their height, shoot dry weight, relative water content, pigment–protein content, the variable fluorescence (Fv) and the maximum quantum efficiency (Fv/Fm) of PSII was recorded. Depending on the allelopathic plants used in this study, the effect of the residues on dodder infestation and basil growth varied significantly. While the use of Z. fabago and D. stramonium residues positively correlated with the suppression of dodder emergence, D. stramonium residue use showed a negative impact on basils’ growth. In contrast, the usage of C. officinalis residues could not diminish dodder infestation, and in dodder-infested basils it decreased plant performance, RWC, pigment and protein content and the maximum quantum efficiency (Fv/Fm) of PSII. Meanwhile, the application of Z. fabago residues to dodder-infested basil plants decreased dodder emergence rate and increased basil plants’ height, dry weight of shoot, relative water content, pigment and protein content, and the maximum quantum efficiency (Fv/Fm) of PSII. Our findings suggest that as an environment-friendly treatment, Z. fabago residues could be used for controlling dodder infestation in basil plants.

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References

  • Aebi H (1984) Catalase in vitro. Methods Enzymol 105:121–126

    CAS  PubMed  Google Scholar 

  • Ahmadi Mousavi E, Manochehri Kalantari KH, Nasibi F, Oloumi H (2017) Effects of carrageenan as elicitor to stimulate defense responses of basil against Cuscuta campestris Yunck. Acta Bot Croat 77:62–69

    Google Scholar 

  • Al-Hakimi AMA (2008) Effect of salicylic acid on biochemical changes in wheat plants under khat leaves residues. Plant Soil Environ 54:288–293

    CAS  Google Scholar 

  • Alsaadawi IS (2001) Allelopathic influence of decomposing wheat residues in agroecosystems. J Crop Prod 4:185–196

    CAS  Google Scholar 

  • Al-Snafi AE (2016) Antiparasitic effects of medicinal plants (part 1)—a review. OSR J Pharm 6:51–66

    Google Scholar 

  • Aly R (2013) Trafficking of molecules between parasitic plants and their hosts. Weed Res 53:231–241

    CAS  Google Scholar 

  • Arnon DI (1949) Copper enzymes in isolated chloroplasts, polyphenoxidase in beta vulgaris. Plant Physiol 24:1–15

    CAS  PubMed  PubMed Central  Google Scholar 

  • Asgharipour MR, Khatamipour M, Razavi-Omrani M (2011) Phytotoxicity of cadmium on seed germination, early growth, proline and carbohydrate content in two wheat varieties. Adv Environ Biol 5:559–565

    CAS  Google Scholar 

  • Balicevic R, Ravlic M, Knezevic M, Maric K, Mikic I (2014) Effect of marigold (Calendula officinalis L.) cogermination, extracts and residues on weed species hoary cress (Cardaria draba (L.) DESV.). Herbologia 14:23–31

    Google Scholar 

  • Balicevic R, Ravlic M, Ravlic I (2015) Allelopathic effect of aromatic and medical plants on Tripleurospermum inodorum (L.) C.H. Schultz Herbol 15:41–53

    Google Scholar 

  • Baytop T (1999) Therapy with medicinal plants in Turkey (past and present). Nobel Tıp Kitapevleri Press, Istanbul

    Google Scholar 

  • Behbahani M, Mohabatkar H, Soltani M (2013) Anti-HIV-1 activities of aerial parts of Ocimum basilicum and its parasite Cuscuta campestris. Ant Antire 5:057–061

    Google Scholar 

  • Beyer WF, Fridovich I (1987) Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions. Anal Biol 161:559–566

    CAS  Google Scholar 

  • Birschwilks M, Haupt S, Hofius D, Neumann S (2006) Transfer of phloem-mobile substances from the host plants to the holoparasite Cuscuta sp. J Exp Bot 57:911–921

    CAS  PubMed  Google Scholar 

  • Bradford MM (1976) A rapid sensitive method for the quantification of microgram quantities of protein utilising the principle of protein-dye binding. Anal Biochem 72:248–254

    CAS  PubMed  Google Scholar 

  • Cakmak I, Horst J (1991) Effect of aluminum on lipid peroxidation, superoxide dismutase, catalase, and peroxidase activities in root tips of soybean (Glycine max). Physiol Plant 83:463–468

    CAS  Google Scholar 

  • Cheeseman J (2007) Hydrogen peroxide and plant stress: a challenging relationship. Plant Stress 1:4–15

    Google Scholar 

  • Cheng F, Cheng Z (2015) Reseach progress on the use of plant allelopathy in agriculture and the physiological and ecological mechanism of allelopathy. Front Plant Sci 6:1–16

    CAS  Google Scholar 

  • Cobb A, Reade J (2010) Herbicides and plant physiology. Crop and Environment Research Centre, Harper Adams University College, Newport, pp 124–126

    Google Scholar 

  • Dawson JH, Musselman LJ, Wolswinkel P, Dorr I (1994) Biology and control of Cuscuta sp. Weed Sci 6:265–317

    Google Scholar 

  • Dinelli G, Bonetti A, Tibiletti E (1993) Photosynthetic and accessory pigments in Cuscuta campestris Yunck. and some host species. Weed Res 33:253–260

    CAS  Google Scholar 

  • Ebrahimi L, Hassannejad S (2015) Allelopathic effects of syrian bean caper (Zygophyllum fabago L.) on seed germination and seedling growth of eastern dodder (Cuscuta monogyna Vahl.). J Biol Environ Sci 7:253–260

    Google Scholar 

  • Einhellig FA (1995) Allelopathy-current status and future goals. In: Inderjit A, Dakshini KMM, Einhellig FA (eds) Allelopathy: organisms, processes, and applications. American Chemical Society Press, Washington, DC, pp 1–24

    Google Scholar 

  • Einhelling FA (2008) Mechanism of action of allelochemicals in allelopathy. Allelopathy: organisms, processes, and applications. American Chemical Society, Washington, DC, pp 96–116

    Google Scholar 

  • El-Amier YA, Abdullah TJ (2014) Allelopathic effect of four wild species on germination and seedling growth of Echinocloa crusgalli L. P. Beauv. Int J Adv Res 2:287–294

    Google Scholar 

  • El-Amier YA, Abbas MA, Dawood SH (2015) Phytotoxic effect of plant extracts from Asteraceae on germination of Echinocloa crusgalli growth. Int J Dev Res 5:4926–4931

    Google Scholar 

  • Elisante F, Tarimo MT, Ndakidemi PA (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 4:2332–2339

    Google Scholar 

  • El-Khatib AA (1999) An ecological overview on the allelopathy of water hyacinth (Eichhornia crassipes), a strategy of weed control. In: Macias FA, Galindo JCG, Molinillo JMG, Cutler HG (eds) Recent advances in allelopathy. A science for the future, vol 1. Services de Publications, Universidad de Cadiz, Cadiz, pp 471–478

    Google Scholar 

  • El-Khatib AA (2000) The ecological significance of allelopathy in the community organization of Alhagi graecorum. Biol Plantarum 43:427–431

    Google Scholar 

  • El-Khatib AA, Hegazy AK, Gala HK (2004) Does allelopathy have a role in the ecology of Chenopodium murale? Ann Bot Fenn 41:37–45

    Google Scholar 

  • Ellis RH, Roberts EH (1981) The quantification of ageing and survival in orthodox seed. Seed Sci Tech 9:337–409

    Google Scholar 

  • El-Shora HM, El-Farrash AH, Kamal H, Abdelrazek A (2015) Positive role of UV radiation in enhancing secondary metabolites production in fenugreek leaves. Int J Sci Res 2015(5):536–543

    Google Scholar 

  • El-Shora H, El-Amir YA, Awad MH (2016) Antimicrobial activity and allelopathic potential of Zygophyllum coccineum L. on Chenopodium album L. Br J Appl Sci Tech 15:1–10

    Google Scholar 

  • Furuhashi T, Kojima M, Sakakibara H, Fukushima A, Yokota HM (2014) Morphological and plant hormonal changes during parasitization by Cuscuta japonica on Momordica charantia. J Plant Int 9:220–232

    CAS  Google Scholar 

  • Genty B, Briantais J, Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta Gen Subj 990:87–92

    CAS  Google Scholar 

  • Gill SS, Tuteja N (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48:909–930

    CAS  PubMed  Google Scholar 

  • Gueta-Dahan Y, Yaniv Z, Zilinskas BA, Ben-Hayyim G (1997) Salt and oxidative stress: similar and specific responses and their relation to salt tolerance in citrus. Planta 203:460–469

    CAS  PubMed  Google Scholar 

  • Hegazy AK, Fadl-Allah EM (1995) Inhibition of seed germination and seedling growth by Cleome droserifolia and allelopathic effect on rhizosphere fungi in Egypt. J Arid Environ 29:3–13

    Google Scholar 

  • Hussain MI, Gonzalez L, Reigosa MJ (2010) Phytotoxic effect of allelochemicals and herbicides on photosynthesis, growth and carbon isotope discrimination in Lactuca sativa. Allelopathy J 26:157–174

    Google Scholar 

  • Jabran KH, Mahajan G, Sardana VS, Chauhan B (2015) Allelopathy for weed control in agricultural systems. Crop Prod 72:57–65

    Google Scholar 

  • Kalaji MH, Guo P (2008) Chlorophyll fluorescence: a useful tool in barley plant breeding programs. In: Sanchez A, Gutierrez SJ (eds) Photochemistry research progress. Nova Publishers, New York, pp 439–463

    Google Scholar 

  • Kalar JS, Bains DS, Gill GS (2009) Studies on the competitive ability of wheat and Chenopodium album L. Ind J Ecol 7:308–310

    Google Scholar 

  • Kochert G (1978) Carbohydrate determination by the phenol sulfuric acid method. In: Hellebust JA, Craigie JS (eds) Handbook of phycological methods. Physiology and biochemistry methods, pp 95–97

  • Krause GH, Weis E (1984) Chlorophyll fluorescence as a tool in plant physiology: II. Interpretation of fluorescence signals. Photosynth Res 5:139–157

    CAS  PubMed  Google Scholar 

  • Lanini W, Kogan M (2005) Biology and management of Cuscuta in crops. Cie Investig Agraria 32:165–179

    Google Scholar 

  • Leather GR, Einhellig FA (1985) Mechanism of allelopathic action in bioassay. In: Thompson AC (ed) The chemistry of allelopathy, biochemical interaction among plants: ACS Symp. Ser. 268. American Chemical Society, Washington. D.C, pp 197–205

    Google Scholar 

  • Lindqvist H, Bornman JF (2002) Influence of time of lifting and storage on the potential photosynthetic efficiency in newly developed leaves of bare root silver birch and common oak. Sci Hortic 94:171–179

    Google Scholar 

  • Matin M, Brown JH, Ferguson H (1989) Leaf water potential, relative water content, and diffusive resistance as screening techniques for drought resistance in barley. Agron J 81:100–105

    Google Scholar 

  • Muzell Trezzi M, Antonio Vidal R, Antonio Balbinot A, Hertwig Bittencourt H, Pedro da Silva A (2016) Allelopathy: driving mechanisms governing its activity in agriculture. J Plant Int 1:53–60

    Google Scholar 

  • Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22:867–880

    CAS  Google Scholar 

  • Nesrine S, El-Darier SM, Taher HM (2012) The allelochemicals effect of zygophyllum album on control of bromus tectorum. J Life Sci 6:182–186

    Google Scholar 

  • Pacifice RE, Davies KJA (1990) Protein degradation as an index of oxidative stress. Methods Enzym 186:485–502

    Google Scholar 

  • Ramasubramania R (2012) Medicinally potential plants of Labiatae (Lamiaceae) family: an overview. Res J Med Plant 6:203–213

    Google Scholar 

  • Rice EL (1984) Allelopathy, 2nd edn. Academic Press, New York

    Google Scholar 

  • Romero-Romero T, Sanchez-Nieto S, Sanjuan-Badillo A, Anaya AL, Cruz-Ortega R (2015) Comparative effects of allelochemical and water stress in roots of Lycopersicon esculentum Mill Plant (Solanaceae). Plant Sci 168:1059–1066

    Google Scholar 

  • Sabagh Nekonam M, Razmjoo J, Kraimmojeni H, Sharifnabi B, Amini H, Bahrami F (2014) Assessment of some medicinal plants for their allelopathic potential against redroot pigweed (Amaranthus retroflexus). J Plant Pro Res 1:90–95

    Google Scholar 

  • Saric-Krsmanovic M, Bozic D, Radivojevic L, Gajic Umiljendic J, Vrbnicanin S (2016) Impact of field dodder (Cuscuta campestris Yunk.) on physiological and anatomical changes in untreated and herbicide-treated alfalfa plants. J Pest Phytol 31:115–120

    Google Scholar 

  • Saric-Krsmanovic M, Bozic D, Radivojevic L, Gajic Umiljendic J, Vrbnicanin S (2017) Effect of Cuscuta campestris parasitism on the physiological and anatomical changes in untreated and herbicide-treated sugar beet. J Environ Sci Health 1:1–5

    Google Scholar 

  • Sayyed A, Shah M (2014) Phytochemistry, pharmacological and traditional uses of Datura stramonium L. J Pharm Phytol 2:123–125

    Google Scholar 

  • Seyyedi M, Rezvani Moghaddam P, Shahriari R, Azad M, Eyshi Rezaei E (2013) Allelopathic potential of sunflower and caster bean on germination properties of dodder (Cuscuta compestris). Afr J Agric Res 8:601–607

    Google Scholar 

  • Singh A, Singh D, Singh NB (2009) Allelochemical stress produced by aqueous leachate of Nicotiana plumbaginifolia Viv. Plant Growth Reg 58:163–171

    CAS  Google Scholar 

  • Soni P, Siddiqui AA, Dwivedi J, Soni V (2012) Pharmacological properties of Datura stramonium L. as a potential medicinal tree: an overview. Asian Pac J Trop Biomed 2:1002–1008

    CAS  PubMed  PubMed Central  Google Scholar 

  • Szakiel A, Ruszkowski D, Grudniak A, Kurek A, Wolska KI, Doligalska M, Janiszowska W (2008) Antibacterial and antiparasitic activity of oleanolic acid and its glycosides isolated from marigold (Calendula officinalis). Planta Med 74:1709–1715

    CAS  PubMed  Google Scholar 

  • Tawaha AM, Turk MA (2003) Allelopathic effects of black mustard (Brassica nigra) on germination and growth of wild barley (Hordeum spontaneum). J Agron Crop Sci 189:298–303

    Google Scholar 

  • Vrbnicanin S, Saric-Krsmanovic M, Bozic D (2013) The effect of Field dodder (Cuscuta campestris Yunck.) on morphological and fluorescence parameters of Giant ragweed (Ambrosia trifida L.). Pestic Phytomed 28:57–62

    Google Scholar 

  • Yang CM, Wang MC, Chang IF, Chou CH (2004) Humic substances affect the activity of chlorophyllase. J Chem Ecol 30:1051–1059

    Google Scholar 

  • Yaripour S, Delnavazi MR, Asgharian P, Valiyari S, Tavakoli S, Nazemiyeh H (2017) A survey on phytochemical composition and biological activity of Zygophyllum fabago from Iran. Adv Pharm Bull 7:109–114

    CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

We appreciate the University of Tabriz for supporting this research.

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Correspondence to Sirous Hassannejad.

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Communicated by G. Araniti.

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Abbasvand, E., Hassannejad, S., Zehtab-Salmasi, S. et al. Physiological and biochemical responses of basil to some allelopathic plant residues and dodder infestation. Acta Physiol Plant 42, 1 (2020). https://doi.org/10.1007/s11738-019-2990-y

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  • DOI: https://doi.org/10.1007/s11738-019-2990-y

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