Interspecific Inhibitory Interference of Nicotiana plumbaginifolia Viv. on Pisum sativum L.

Journal of Plant Growth Regulation - Tập 40 - Trang 2037-2048 - 2020
Waseem Mushtaq1, Quratul Ain1, M. B. Siddiqui1, Hesham F. Alharby2, Khalid Rehman Hakeem2,3
1Allelopathy Laboratory, Department of Botany, Aligarh Muslim University, Aligarh, India
2Department of Biological Sciences, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia
3Princess Dr Najla Bint Saud Al- Saud Center for Excellence Research in Biotechnology, King Abdulaziz University, Jeddah, Saudi Arabia

Tóm tắt

Roots of weeds that are left behind in the soil after removal of their aerial parts can reduce the growth of crops. Here we conducted an assessment to evaluate the allelopathic interference of Nicotiana plumbaginifolia roots and its rhizosphere soil on the growth of Pisum sativum L., identification of chemicals involved, the role of charcoal, the role of N and other macronutrients. Growth responses of P. sativum were analysed for (a) rhizosphere soil with and without N supplementation and (b) soil amendment with Nicotiana roots. Scanning electron microscopy-energy dispersive spectrometry (SEM–EDS) analysis of the rhizosphere soil was conducted to look for concentration of essential nutrients. Rhizosphere soil showed an inhibitory effect even with N supplementation. SEM–EDS showed a healthy concentration of essential nutrients. Root residues of Nicotiana integrated with soil do cause a reduction in seedling length (root length, shoot length) and dry biomass of recipient plant. However, a partial alleviation in growth inhibition occurred upon the addition of activated charcoal. Soils amended with root residues were rich in phenolics as compared to control. Overall, 34 compounds were reported upon GC–MS analysis which can be considered responsible for the allelopathic suppression of P. sativum. The chief component was guanosine (26.21%) followed by n-hexadecanoic acid (18.61%), oleic acid (18.29%), palmitoleic acid (4.80%), -(-)nicotine (5.09%) and solasodine (2.54%). These results show a definite role of putative allelochemicals that exerted allelopathic effects on P. sativum.

Tài liệu tham khảo

Allen SE (1989) Chemical analysis of ecological materials. Blackwell, London Arora N, Pandey-Rai S (2014) GC–MS analysis of the essential oil of Celastrus paniculatusWilld.seeds and antioxidant, anti-inflammatory study of its various solvent extracts. Ind Crops Prod 61:345–351 Bais HP, Park SW, Weir TL, Callaway RM, Vivanco JM (2004) How plants communicate using the underground information superhighway. Trends Plant Sci 9:23–32 Batish DR, Singh HP, Rana N, Kohli RK (2006) Assessment of allelopathic interference of Chenopodium album through its leachates, debris extracts, rhizosphere and amended soil. Arch Agron Soil Sci 52:705–715 Batish DR, Lavanya K, Singh HP, Kohli RK (2007) Root-mediated allelopathic interference of Nettle-leaved Goosefoot (Chenopodium murale) on wheat (Triticumaestivum). J Agron Crop Sci 193:37–44 Batish DR, Kaur S, Singh HP, Kohli RK (2009) Role of root-mediated interactions in phytotoxic interference of Ageratum conyzoides with rice (Oryza sativa). Flora 204(5):388–395 Bertin C, Yang X, Weston LA (2003) The role of root exudates and allelochemicals in the rhizosphere. Plant Soil 256(1):67–83 Blum U, Shafer SR, Lehman ME (1999) Evidence for inhibitory allelopathic interactions involving phenolic acids in field soils: concepts vs. an experimental model. Crit Rev Plant Sci 18:673–693 Castells E, Penuelas J, Valentine DW (2005) Effects of plant leachates from four boreal understorey species on soil N mineralization, and white Spruce (Piceaglauca) germination and seedling growth. Ann Bot 95:1247–1252 Chen LC, Wang SL (2012) Allelopathic behaviour of Chinese fir from plantations of different ages. Forestry 86(2):225–230 Cheremisinoff PN, Ellerbusch F (1978) Carbon adsorption handbook. Ann Arbor Science Publishers, Ann Arbor, MI de Candolle AP (1832) Physiologievegetale. BechetJeune, Paris Dallali S, Rouz S, Aichi H, Hassine HB (2017) Phenolic contentand allelopathic potential of leavesoil rhizosphere soilaqueous extracts of white horehound (Maribumvulgare L.). J New Sci 39(3):2106–2120 Djurdjevic L, Popovic Z, Mitrovic M, Pavlovic P, Jaric S, Oberan L, Gajic G (2008) Dynamics of bioavailable rhizosphere soil phenolics and photosynthesis of Arum maculatumL. in a lime-beech forest. Flora 203:590–601 Duncan DB (1955) Multiple range and multiple F-tests. Biometrics 11:1–42 Eckart E (2008) Solanaceae and convolvulaceae: secundary metabolites. Springer-Verlag, Berlín, p p79 El-khatib AA, Hegazy AK, Galal HK (2004) Allelopathy in the rhizosphere and amended soil of Chenopodium murale L. Weed BiolManag 4(1):35–42 Food and Agriculture Organization (FAO) (1974) FAO-UNESCO soils map of the World, 1st edn. UNESCO, Paris Kjeldahl J (1883) NeueMethodezurBestimmung des Stickstoffs in organischenKorpern (New method for the determination of nitrogen in organic substances). Zeitschrift fur analytischeChemie 22(1):366–383 Kong CH, Li HB, Hu F, Xu XH (2006) Allelochemicals released by rice roots and residues in soil. Plant Soil 288:47–56 Li ZH, Wang Q, Ruan X, Pan CD, Jiang DA (2010) Phenolics and plant allelopathy. Molecules 15(12):8933–8952 Liu Q, Lu D, Jin H, Yan Z, Li X, Yang X, Guo H, Qin B (2014) Allelochemicals in the rhizosphere soil of Euphorbia himalayensis. J Agric Food Chem 62(34):8555–8561 MahallBE CRM (1991) Root communication among desert shrubs. Proc Natl Acad Sci USA 88:874–876 McCully E (1999) Roots in soil: unearthing the complexities of roots and their rhizospheres. Annu Rev Plant Physiol Plant MolBiol 50:695–718 Mizutani J (1999) Selected allelochemicals. Crit Rev Plant Sci 18:653–671 Mushtaq W, Siddiqui MB (2018) Allelopathy in Solanaceae plants. J Plant Prot Res 58(1):1–7 Mushtaq W, Mehdizadeh M, Siddiqui MB, Ozturk M, Jabran K, Altay V (2020) Phytotoxicity of above-ground weed residue against some crops and weeds. Pak J Bot 52(3):1–10. https://doi.org/10.30848/PJB2020-3(40) Mushtaq W, Quratul-Ain SMB, Hakeem KR (2020) Allelochemicals change macromolecular content of some selected weeds. South Afr J Bot 130:77–184. https://doi.org/10.1016/j.sajb.2019.12.026 Mushtaq W, Quratul-Ain SMB, Hakeem KR (2019) Cytotoxic allelochemicals induce ultrastructural modifications in Cassia tora L. and mitotic changes in Allium cepa L.: A weed versus weed allelopathy approach. Protoplasma 256:857–871 Mushtaq W, Ain Q, Siddiqui MB (2018) Screening of allelopathic activity of the leaves of Nicotiana plumbaginifoliaViv.on some selected crops in Aligarh, Uttar Pradesh India. Int J PhotochemPhotobio 2(1):1–4 Nardi S, Concheri G, Pizzeghello D, Sturaro A, Rella R, Parvoli G (2000) Soil organic matter mobilization by root exudates. Chemosphere 5:653–658 Prati D, Bossdorf O (2004) Allelopathic inhibition of germination by Alliariapetiolata (Brassicaceae). Am J Bot 91:285–288 Proestos C, Sereli D, Komaitis M (2006) Determination of phenolic compounds in aromatic plants by RP-HPLC and GC-MS. Food Chem 95:44–52 Rice EL (1984) Allelopathy, 2nd edn. Academic Press, New York Reigosa MJ, Souto XC, Gonz’lez L (1999) Effect of phenolic compounds on the germination of six weeds species. J Chem Ecol 28:83–88 Rovira AD (1969) Plant root exudates. Bot Rev 35:35–57 Schreiner O, Reed HS (1907) The production of deleterious excretions by roots. Bull Torrey Bot Club 34:279–303 Sharma R, Patel KS, Lata L, Milosh H (2016) Characterization of Urban Soil with SEM-EDX. Am J AnalytChem 7(10):724–735 Singh A, Singh D, Singh NB (2009) Allelochemical stress produced by aqueous leachate of Nicotiana plumbaginifoliaViv. Plant Growth Regul 58:163–171 Singh A, Singh D, Singh NB (2015) Allelopathic activity of Nicotiana plumbaginifolia at various phenological stages on sunflower. Allelopathy J 36(2):315–325 Sisodia S, Siddiqui MB (2009) Allelopathic potential of rhizosphere soil of Croton bonplandianum on growth and establishment of some crop and weed plants. Afr J Agr Res 4(5):461–467 Swain T, Hillis WE (1959) The phenolic constituents of Prunusdomestica I. The quantitative analysis of constituents JSci Food Agr 10:63–68 Tuyen PT, Xuan TD, TuAnh TT, Van Mai T, Ahmad A, Elzaawely AA, Khanh TD (2018) Weed suppressing potential and isolation of potent plant growth inhibitors from CastaneacrenataSieb. etZucc. Molecules 23(2):345 Walkley A, Black IA (1934) An examination of the Digtjareff method for determining soil organic matter and a proposed modification of chromic acid titration method. Soil Sci 37:29–38 Walker TS, Bais HP, GrotewoldE VJM (2003) Root exudation and rhizosphere biology. Plant Physiol 132:44–51 Weston LA, Ryan PR, Watt M (2012) Mechanisms for cellular transport and release of allelochemicals from plant roots into the rhizosphere. J Exp Bot 63(9):3445–3454 Xuan TD, Tawata S, Khanh TD, Chung IM (2005) Decomposition of allelopathic plants in soil. J Agron Crop Sci 191:162–171