Abstract
Excessive use of chemical herbicides has led to human health and environmental problems. However, environmentally friendly strategies for weed management are changing them competition in favor of crops. In this regard, the effects of different aqueous extract concentrations of root and shoot of black cumin on germination and initial growth of charlock mustard (Sinapis arvensis L.) and common wheat (Triticum aestivum L.) were compared in 2020 in the Agriculture Laboratory of the Faculty of Agriculture, Shahrekord University. The results showed that increasing the concentration of black cumin extracts increased hydrogen peroxide, lipid peroxide, and proline and decreased the germination parameters, mitotic index, cell viability, and vigor index of charlock mustard. Black cumin extract, even with the lowest concentration, restricted the vigor index of charlock mustard with a steeper slope than the wheat (18 and 4.5%, respectively). The presence of critical inhibitory compounds in black cumin extract, including polyphenols (such as tricarboxylic acids), flavonoids, and alkaloids (such as magnoflorine, myristicin, norargemonine, and nigellamine), restricts the germination indices of charlock mustard. Additionally, terpenoids such as cycloartenol, bisabolol, limonene, P-cymene, O-cymene, 1,8-cineole, myrcene, carvacrol, and thymol, which were higher in the shoot than the root, strengthen the inhibitory effects of black cumin extract. In general, due to the strong impact of black cumin extract on stopping the growth of charlock mustard weed and little impact on wheat seedlings, black cumin can be introduced as a viable candidate for natural herbicide production. In addition, its cultivation in rotation with a wheat crop, helps control charlock mustard and reduce the use of synthetic herbicides.
Graphic abstract
Similar content being viewed by others
References
Ahmad A, Husain A, Mujeeb M, Khan SA, Najmi AK, Siddique NA, Damanhouri ZA, Anwar F (2013) A review on therapeutic potential on Nigella sativa: a miracle herb. Asian Pac J Trop Biomed 3:337–352
Aliverdi A, Rashed-Mohasel MR, Zand E, Nasiri-Mahalati M (2009) Increased foliar activity of clodinafop-propargyl and/or tribenuronmethyl by surfactants and their synergistic action on wild oat (Avena ludoviciana) and wild mustard (Sinapis arvensis). Weed Biol Manag 9:292–299
Amoo SO, Ojo AU, Staden JV (2008) Allelopathic potential of Tetrapleura tetraptera leaf extracts on early seedling growth of five agricultural crops. S Afr J Bot 74:149–152
Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol 55:373–399
Appiah KS, Mardani HK, Osivand A, Kpabitey S, Amoatey CA, Oikawa Y, Fujii Y (2017) Exploring alternative use of medicinal plants for sustainable weed management. Sustainability 9:1468. https://doi.org/10.3390/su9081468
Ayala A, Munoz MF, Arguelles S (2014) Lipid peroxidation: Production, metabolism, and signaling mechanisms of malondialdehyde and 4-Hydroxy-2-Nonenal. Oxid Med Cell Longev 2014:360438. https://doi.org/10.1155/2014/360438
Azadbakht A, Mahmoodi S, Amraie R, Amraei B, Nasrollahi H (2013) Evaluation the allelopathic effects of aerial and underground extract of sunflower (Helianthus annus L.) on germination charactristics and seedling growth of Hoary cress (Cardaria draba). Ann Biol Res 4:188–195
Azirak S, Karaman S (2008) Allelopathic effect of some essential oils and components on germination of weed species. Acta Agric Scand B Soil Plant Sci 58:88–92
Badmus A, Afolayan A (2012) Allelopathic potential of Arctotis arctotoides (L.f.) Hoffm aqueous extracts on the germination and seedling growth of some vegetables. Afr J Biotechnol 47:10711–10716
Bates L, Waldren RP, Teare ID (1973) Rapid determination of free proline for water stress studies. Plant Soil 3:205–207
Beres I, Kazinczi G (2000) Allelopathic effects of shoot extracts and residues of weeds on field crops. Allelopathy J 7:93–98
Berlin J, Rugenhagen C, Greidziak N, Kuzovkina IN (1993) Biosynthesis of serotonin and β-carboline alkaloids in hairy root cultures of Peganum harmala. Phytochemistry 18:593–597
Bertin C, Yang X, Weston LA (2003) The role of root exudates and allelochemicals in the rhizosphere. Plant Soil 256:67–83
Bogatek R, Orazk K, Gniazdowska A (2006) Allelopathic effects of sunflower extracts on mustard seed germination and seedling growth. Biol Plant 50:156–158. https://doi.org/10.1007/s10535-005-0094-6
Bojović BM, Jakovljević DZ, Ćurcić SS, Stanković MS (2018) Phytotoxic potential of common nettle (Urtica dioica L.) on germination and early growth of cereals and vegetables. Allelopathy J 43:175–186
Bruno L, Talarico E, Cabeiras-Freijanes L, Madeo ML, Muto A, Minervino M, Lucini L, Miras-Moreno B, Sofo A, Araniti F (2021) Coumarin interferes with polar auxin transport altering microtubule cortical array organization in Arabidopsis thaliana (L.) [Heynh.] root apical meristem. Int J Mol Sci 22(14):7305. https://doi.org/10.3390/ijms22147305. (PMID:34298924)
Burguieres E, McCue P, Kwon YI, Shetty K (2007) Effect of vitamin C and folic acid on seed vigor response and phenolic-linked antioxidant activity. Bioresour Technol 98:1393–1404
Caser M, Demasi S, Caldera F, Dhakar NK, Trotta F, Scariot V (2020) Activity of ailanthus altissima (Mill.) swingle extract as a potential bioherbicide for sustainable weed management in horticulture. Agronomy 10:965–982
Cheng F, Cheng Zh (2015) Research progress on the use of pant allelopathy in agriculture and the physiological and ecological mechanisms of allelopathy. Plant Sci 6:1020–1036. https://doi.org/10.3389/fpls.2015.01020
Chon SU, Jang HG, Kim DK, Kim YM, Boo HO, Kim YJ (2005) Allelopathic potential in lettuce (Lactuca Sativa L.) plants. Sci Hortic 106:309–317
Chung IM, Ahn JK, Yun SJ (2001) Assessment of allelopathic potential of barnyard grass (Echinochloa crus-galli) on rice (Oryza sativa L.) cultivars. Crop Prot 20:921–928
Cruz-Ortega R, Lara-Nunez A, Anaya AL (2007) Allelochemical stress can trigger oxidative damage in receptor plants. Plant Signal Behav 2:269–270
Debra E, Matika F, Loake GJ (2014) Redox regulation in plant immune function. Antioxid Redox Signal 21:1373–1388. https://doi.org/10.1089/ars.2013.5679
Dmitrović S, Simonović A, Mitić N, Savić J, Cingel A, Filipović B, Ninković S (2015) Hairy root exudates of allelopathic weed Chenopodium murale (L.) induce oxidative stress and down-regulate core cell cycle genes in Arabidopsis and wheat seedlings. Plant Growth Regul 75:365–382. https://doi.org/10.1007/s10725-014-9959-z
Duman I (2006) Effects of seed priming with PEG or K3PO4 on germination and seedling growth in lettuce. Pak J of Bio Sci 11:923–928. https://doi.org/10.3923/pjbs.2006.923.928
Ehlers BK, Thompson J (2004) Do co-occurring plant species adapt to one another? The response of Bromus erectus to the presence of different Thymus vulgaris chemotypes. Oecologia 141:511–518
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
FAO (2019) Crops and livestock products. https://www.fao.org/faostat/en/#data. Accessed 26 January 2022.
Fardet A, Rock E, Christian R (2008) Is the in vitro antioxidant potential of whole grain cereals and cereal produces well reflected in vivo. J Cereal Sci 48:258–276
Farooq M, Hussain M, Habib MM, Khan MS, Ahmad I, Farooq S, Siddique KHM (2020) Influence of seed priming techniques on grain yield and economic returns of bread wheat planted at different spacings. Crop Pasture Sci 71:725–738. https://doi.org/10.1071/CP2006
Ferguson JJ, Rathinasabapathi B, Chase CA (2009) Allelopathy: How plants suppress other plants. Institute of Food and Agricultural Sciences, University of Florida, Gainesville, The Horticultural Sciences Department
Gajewska E, Sklodowska M, Slaba M, Mazur J (2006) Effect of nickel on antioxidative enzyme activities, proline and chlorophyll contents in wheat shoots. Biol Plant 50:653–659
Guevara ML, Guevara JJ, Carranza P, Espinosa HR, Velasco CEO (2018) Phenolic compounds: a good choice against chronic degenerative diseases. Stud Nat Prod Chem 59:79–108. https://doi.org/10.1016/B978-0-444-64179-3.00003-7
Hussain M, Farooq S, Jabran K, Ijaz M, Sattar A, Hassan W (2016) Wheat sown with narrow spacing results in higher yield and water use efficiency under deficit supplemental irrigation at the vegetative and reproductive stage. Agronomy 6:1–13
Ikic I, Maricevic M, Tomasovic S, Gunjaca J, Sarcevic Z, Arcevic H (2012) The effect of germination temperature on seed dormancy in creation-grown winter wheats. Euphytica 188:25–34
Jabran K, Mahmood K, Melander B, Bajwa AA, Kudsk P (2017) Weed dynamics and management in wheat. Adv Agron 145:97–166
Kabir Y, Akasaka-Hashimoto Y, Kubota K, Komai M (2020) Volatile compounds of black cumin (Nigella sativa L.) seeds cultivated in Bangladesh and India. Heliyon 6:e05343. https://doi.org/10.1016/j.heliyon.2020.e05343
Karna SKL (2013) Phytochemical screening and gas chromatography–mass spectrometry and analysis of seed extract of Nigella sativa L. Int J Chem Stud 1:183–188
Leather GR, Einhellig FA (1988) Bioassay of naturally occurring allelochemical for toxicity. J Chem Ecol 14:1821–1828
Lyu SW, Blum U, Gerig TM, O’Brien TE (1990) Effects of mixtures of phenolic acids on phosphorus uptake of cucumber seedling. J Chem Ecol 16:2559–2567
Madadi E, Fallah S, Sadeghpour A, Barani-Beiranvand H (2022) Exploring the use of chamomile (Matricaria chamomilla L.) bioactive compounds to control flixweed (Descurainia sophia L.) in bread wheat (Triticum aestivum L.): Implication for reducing chemical herbicide pollution. Saudi J Biol Sci. 29(11):103421. https://doi.org/10.1016/j.sjbs.2022.103421
Mahmoud SA, Singh SD, Muralikrishna KS (2016) Allelopathy in jatropha plantation: Effects on seed germination, growth and yield of wheat in north-west India. Agric Ecosyst Environ 231:240–245
Melander B, Jabran Kh, De Notaris Ch, Znova L, Green O, Olesen JE (2018) Inter-row hoeing for weed control in organic spring cereals-Influence of inter-row spacing and nitrogen rate. Eur J Agron 101:49–56
Milthrope FL (1995) Change in the drought resistance of wheat seedling during germination. Ann Bot 14:79–86
Mominul Islam AKM, Yeasmin S, Qasem JR, Juraimi AS (2018) Allelopathy of medicinal plants: current status and future prospects in weed management. Agric Sci 9:1569–1588
Motmainna M, Juraimi AS, Uddin MK, Asib NB, Islam AKMM, Ahmad-Hamdani MS, Hasan M (2021) Phytochemical constituents and allelopathic potential of Parthenium hysterophorus L. in comparison to commercial herbicides to control weeds. Plants 10:1445. https://doi.org/10.3390/plants10071445
Mujeeb F, Bajpai P, Pathak N (2014) Phytochemical evaluation, antimicrobial activity, and determination of bioactive components from leaves of Aegle marmelos. BioMed Res Int 2014:497606. https://doi.org/10.1155/2014/497606
Nag S, Saha K, Choudhuri MA (2000) A rapid and sensitive assay method for measuring amine oxidase based on hydrogen peroxide–titanium complex formation. Plant Sci 157:157–163. https://doi.org/10.1016/S0168-9452(00)00281-8
Nikneshan P, Karimmojeni H, Moghanibashi M, Hosseini N (2011) Allelopathic potential of sunflower on weed management in sanflower and wheat. Aust J Crop Sci 5:1434–1440
Ozpinar H, Dag S, Yigit E (2017) Alleophatic effects of benzoic acid, salicylic acid and leaf extract of Persica vulgaris Mill. (Rosaceae). S Afr J Bot 108:102–109
Parvez SS, Parvez MM, Nishihara E, Gemma H, Fujii Y (2003) Tamarindus indica (L.) leaf is a source of allelopathic substance. Plant Growth Regul 40:107–115. https://doi.org/10.1023/A:1024237426416
Petersen J, Belz R, Walker F, Hurle K (2001) Weed suppression by release of Isothiocyanates from turin-rape mulch. Agron J 93:37–43
Planchais S, Glab N, Inze D, Bergounioux C (2000) Chemical inhibitors: a tool for plant cell cycle studies. FEBS Lett 47:78–83. https://doi.org/10.1016/S0014-5793(00)01675-6
Pudełko K, Majchrzak L, Narozna D (2014) Allelopathic effect of fibre hemp (Cannabis sativa L.) on monocot and dicot plant species. Ind Crops Prod 56:191–199
Qasem JR (2017) A Survey on the phytotoxicity of common weeds, wild grown species and medicinal plants on wheat. Allelopathy J 42:179–194
Qasim M, Fujii Y, Ahmed MZ, Aziz I, Watanabe KN, Khan MA (2019) Phytotoxic analysis of coastal medicinal plants and quantification of phenolic compounds using HPLC. Plant Biosyst 153:767–774. https://doi.org/10.1080/11263504.2018.1549607
Rehim A, Hussain M, Abid M, Zia-Ul-Haq M, Ahmad S (2012) Phosphorus use efficiency of Trititicum aestivum L. As affected by band placement of phosphorus and farmyard manure on calcareous soils. Pakistan J Bot 44:1391–1398
Ren Y, Wang W, He J, Zhang L, Wei Y, Yang M (2020) Nitric oxide alleviates salt stress in seed germination and early seedling growth of pakchoi (Brassica chinensis L.) by enhancing physiological and biochemical parameters. Ecotoxicol Environ Saf 187:109785
Shahzad M, Farooq M, Hussain M (2016) Weed spectrum in different wheat-based cropping systems under conservation and conventional tillage practices in Punjab, Pakistan. Soil till Res 163:71–79. https://doi.org/10.1016/j.still.2016.05.012
Shahzad M, Jabran K, Hussain M, Raza MAS, Wijaya L, El-Sheikh MA, Alyemen MN (2021) The impact of different weed management strategies on weed flora of wheat-based cropping systems. PLoS ONE 16:e0247137
Sothearith Y, Appiah KS, Mardani H, Motobayashi T, Yoko S, Eang Hourt K, Sugiyama A, Fujii Y (2021) Determination of the allelopathic potential of Cambodia’s medicinal plants using the dish pack method. Sustainability 13:9062–9072. https://doi.org/10.3390/su13169062
Teklic T, Engler M, Cesar V, Lepedua H, Paraikovic N, Loncaric Z, Tolfa I, Marotti T, Mikac N, Zarkovic N (2008) Influence of excess copper on lettuce (Lactuca sativa L.) grown in soil and nutrient solution. J Food Agric Environ 6:439–444
Tigre RC, Silva NH, Santos MG, Honda NK, Falcao EPS, Pereira EC (2012) Allelopathic and bioherbicidal potential of Cladonia verticillaris on the germination and growth of lactuca sativa. Ecotoxicol Environ Saf 84:125–132
Turk MA, Tawaha AM (2002) Inhihitory effects of aqueous extracts of black mustard on germination and growth of lentil. Pak J Agric 1:28–30
United Nations, Department of Economic and Social Affairs, Population Division (2019) World Population Prospects. https://population.un.org/wpp/2020. Accessed 26 April 2020.
Wardle DA, Nicholson KS, Rahman A (1996) Use of a comparative approach to identify allelopathic potential and relationship between allelopathy bioasays and competition experiments for ten grassland and plant species. J Chem Ecol 22:933–948. https://doi.org/10.1007/BF02029946
Yan ZQ, Wang DD, Ding L, Cui HY, Jin H, Yang XY, Yang JSh, Qin B (2015) Mechanism of artemisinin phytotoxicity action: Induction of reactive oxygen species and cell death in lettuce seedlings. Plant Physiol Biochem 88:53–59. https://doi.org/10.1016/j.plaphy.2015.01.010
Yang CM, Chang F, Li SJ, Chou CH (2004) Effects of three allelopathic phenolics on chlorophyll accumulation of rice (Oryza sativa) seedlings: II. Stimulation of consumption-orientation. Bot Bull Acad Sin 45:119–125
Zammali I, Dabbous A, Youssef S, Ben Hamed KB (2022) Effects of chemical priming on the germination of the ornamental halophyte lobularia maritima under NaCl salinity. Seeds 1:99–109. https://doi.org/10.3390/seeds1020009
Zargar M, Kavhiza NJ, Bayat M, Pakina E (2021) Wild mustard (Sinapis arvensis) competition and control in rain-fed spring wheat (Triticum aestivum L.). Agronomy 11:2306. https://doi.org/10.3390/agronomy11112306
Zhao J, Yang Z, Zou J (2022) Allelopathic effects of sesame extracts on seed germination of moso bamboo and identification of potential allelochemicals. Sci Rep 12(1):6661. https://doi.org/10.1038/s41598-022-10695-x
Acknowledgements
The authors would like to thank Shahrekord University for providing financial support (grant # 99GRN31M731 to SF).
Author information
Authors and Affiliations
Contributions
EM designed the analysis, collected the data, and contributed to analysis, writing-original draft preparation, and investigation. SF designed the analysis and contributed to methodology, writing-review and editing, conceptualization, and supervision. AS contributed to writing-review and editing, conceptualization, and project advisory committee. HB-B collected the data and contributed to writing-review and editing and project advisory committee.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Additional information
Editorial responsibility: Samareh Mirkia.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Madadi, E., Fallah, S., Sadeghpour, A. et al. Black cumin bioactive compounds as eco-friendly novel green herbicides in wheat cropping: application to reduce chemical herbicides pollution. Int. J. Environ. Sci. Technol. 20, 7325–7342 (2023). https://doi.org/10.1007/s13762-023-04980-z
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s13762-023-04980-z