Rye (Secale cereale L.) and squarrose clover (Trifolium squarrosum L.) cover crops can increase their allelopathic potential for weed control when used mixed as dead mulch

Submitted: 12 March 2021
Accepted: 31 May 2021
Published: 31 August 2021
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Cover crops are essential tools in agro-ecosystems for reducing the reliance on synthetic inputs and associated environmental risks. Alongside their benefits to soil fertility, cover crops can control weeds by their competitive and allelopathic attributes. Laboratory and field experiments were conducted to assess the allelopathic potential of two cover crop species, rye (Secale cereale L.) and squarrose clover (Trifolium squarrosum L.), alone or in a mixture, on seed germination and growth of arable weeds. Aqueous extracts of the two cover crops and their mixture were tested in a bioassay on Conyza canadensis (L). Cronq., Amaranthus retroflexus L. and Digitaria sanguinalis (L.) Scop. In vitro effects of aqueous extracts varied in a dose-dependent manner, with cover crops and weed species. All three extracts were able to reduce the germination of A. retroflexus (–87%) considerably. Inhibitory effects by rye and mixture extracts on radicle growth of all weed species ranged between 51 and 82%. Rye extract was the best at reducing shoot length of C. canadensis and D. sanguinalis (–39 to 44%), while squarrose clover was more effective on A. retroflexus (–79%). Plant extracts also delayed the germination time of weed species with a substantial effect of the mixture on C. canadensis seeds. In the field experiment, no significant weed suppression was provided by cover crop residues incorporated as green manure compared to control plots, despite tillage being more effective in reducing weed density than no-till. Still, the mulch of the mixture controlled weed emergence significantly better than single cover crop mulches. The chemical characterization of cover crop residues, both shoots and roots, revealed a notable richness of allelopathic phenolic acids and flavonoids, which may constitute potential natural herbicides through slow decomposition. From the analysis of the aqueous extracts, other non-analysed and/or unidentified water-soluble allelopathic compounds should underlie the phytotoxicity observed in vitro, at least for rye. For cover crop mixture, positive interactions among plant materials leading to a better release of allelochemicals and weeding effectiveness are discussed according to chemical profiles and field data. Our study demonstrated the allelopathic activity of the cover crops and their potential to be included in weed management strategies according to cropping system needs. Additional trials are needed to confirm the performance of cover crop residues under field conditions.

Highlights
- Rye and squarrose clover are cover crops with potential allelopathic effects.
- Aqueous extracts of residues of rye, squarrose clover, and their mixture reduced and/or slowed weed germination of A. retroflexus and C. canadensis in the in vitro bioassays.
- Depending on the concentration of residues, the aqueous extracts had inhibitory effects on radicle and shoot growth of A. retroflexus, C. canadensis, and D. sanguinalis.
- The mulch of a mix of rye and squarrose clover under field conditions suppressed weeds better than the single species.

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Abou Chehade L, Antichi D, Martelloni L, Frasconi C, Sbrana M, Mazzoncini M, Peruzzi A, 2019. Evaluation of the agronomic performance of organic processing tomato as affected by different cover crop residues management. Agronomy 9:504. DOI: https://doi.org/10.3390/agronomy9090504
Álvarez-Iglesias L, Puig CG, Garabatos A, Reigosa MJ, Pedrol N, 2014. Vicia faba aqueous extracts and plant material can suppress weeds and enhance crops. Allelopathy J. 34:299.
Álvarez-Iglesias L, Puig CG, Revilla P, Reigosa MJ, Pedrol N, 2018. Faba as green manure for field weed control in maize. Weed Res. 58:437-49. DOI: https://doi.org/10.1111/wre.12335
Annett R, Habibi HR, Hontela A, 2014. Impact of glyphosate and glyphosate‐based herbicides on the freshwater environment. J. Appl. Toxicol. 34:458-79. DOI: https://doi.org/10.1002/jat.2997
Baraibar B, Hunter MC, Schipanski ME, Hamilton A, Mortensen DA, 2018. Weed suppression in cover crop monocultures and mixtures. Weed Sci. 66:121-33. DOI: https://doi.org/10.1017/wsc.2017.59
Barberi P, Mazzoncini M, 2001. Changes in weed community composition as influenced by cover crop and management system in continuous corn. Weed Sci. 49:491-9. DOI: https://doi.org/10.1614/0043-1745(2001)049[0491:CIWCCA]2.0.CO;2
Bastiaans L, Paolini R, Baumann DT, 2008. Focus on ecological weed management: what is hindering adoption? Weed Res. 48:481-91. DOI: https://doi.org/10.1111/j.1365-3180.2008.00662.x
Baucom RS, 2019. Evolutionary and ecological insights from herbicide‐resistant weeds: what have we learned about plant adaptation, and what is left to uncover? New Phytol. 223:68-82. DOI: https://doi.org/10.1111/nph.15723
Beninger CW, Hall JC, 2005. Allelopathic activity of luteolin 7-O-β-glucuronide isolated from Chrysanthemum morifolium L. Biochem. Syst. Ecol. 33:103-11. DOI: https://doi.org/10.1016/j.bse.2004.06.016
Blanco‐Canqui H, Claassen MM, Presley DR, 2012. Summer cover crops fix nitrogen, increase crop yield, and improve soil-crop relationships. Agron. J. 104:137-47. DOI: https://doi.org/10.2134/agronj2011.0240
Carlsen SC, Kudsk P, Laursen B, Mathiassen SK, Mortensen AG, Fomsgaard IS, 2009. Allelochemicals in rye (Secale cereale L.): cultivar and tissue differences in the production of benzoxazinoids and phenolic acids. Nat. Prod. Commun. 4:199-208. DOI: https://doi.org/10.1177/1934578X0900400206
Cheng F, Cheng Z, 2015. Research progress on the use of plant allelopathy in agriculture and the physiological and ecological mechanisms of allelopathy. Front. Plant Sci. 6:1020. DOI: https://doi.org/10.3389/fpls.2015.01020
Chou CH, Patrick ZA, 1976. Identification and phytotoxic activity of compounds produced during decomposition of corn and rye residues in soil. J. Chem. Ecol. 2:369-87. DOI: https://doi.org/10.1007/BF00988283
Copaja SV, Villarroel E, Bravo HR, Pizarro L, Argandoña VH, 2006. Hydroxamic acids in Secale cereale L. and the relationship with their antifeedant and allelopathic properties. Z. Naturforsch. C 61:670-6. DOI: https://doi.org/10.1515/znc-2006-9-1010
De Bruin JL, Porter PM, Jordan, NR, 2005. Use of a rye cover crop following corn in rotation with soybean in the upper Midwest. Agron. J. 97:587-98. DOI: https://doi.org/10.2134/agronj2005.0587
Dhima KV, Vasilakoglou IB, Eleftherohorinos IG, Lithourgidis AS, 2006. Allelopathic potential of winter cereals and their cover crop mulch effect on grass weed suppression and corn development. Crop Sci. 46:345-52. DOI: https://doi.org/10.2135/cropsci2005-0186
Falquet B, Gfeller A, Pourcelot M, Tschuy F, Wirth J, 2015. Weed suppression by common buckwheat: a review. Environ. Control Biol. 53:1-6. DOI: https://doi.org/10.2525/ecb.53.1
Farooq M, Khan I, Nawaz A, Cheema MA, Siddique KH, 2020. Using sorghum to suppress weeds in autumn planted maize. Crop Prot. 133:105162. DOI: https://doi.org/10.1016/j.cropro.2020.105162
Fernández-Aparicio M, Emeran AA, Rubiales D, 2010. Inter-cropping with berseem clover (Trifolium alexandrinum) reduces infection by Orobanche crenata in legumes. Crop Prot. 29:867-71. DOI: https://doi.org/10.1016/j.cropro.2010.03.004
Freibauer A, Rounsevell MD, Smith P, Verhagen J, 2004. Carbon sequestration in the agricultural soils of Europe. Geoderma 122:1-23. DOI: https://doi.org/10.1016/j.geoderma.2004.01.021
Gerhards R, Schappert A, 2020. Advancing cover cropping in temperate integrated weed management. Pest Manage. Sci. 76:42-6. DOI: https://doi.org/10.1002/ps.5639
Hazrati H, Fomsgaard IS, Kudsk P, 2020. Root-exuded benzoxazinoids: uptake and translocation in neighboring plants. J. Agric. Food Chem. 68:10609-17. DOI: https://doi.org/10.1021/acs.jafc.0c04245
Hussain MI, Gonzalez L, Souto XC, Reigosa MJ, 2011. Ecophysiological responses of three native herbs to phytotoxic potential of invasive Acacia melanoxylon R. Br. Agrofor. Syst. 83:149-66. DOI: https://doi.org/10.1007/s10457-011-9433-0
Jia C, Kudsk P, Mathiassen SK, 2006. Joint action of benzoxazinone derivatives and phenolic acids. J. Agric. Food Chem. 54:1049-57. DOI: https://doi.org/10.1021/jf051156r
Kaspar TC, Radke, JK, Laflen, JM, 2001. Small grain cover crops and wheel traffic effects on infiltration, runoff, and erosion. J. Soil Water Conserv. 56:160-4.
Kolodziejczyk-Czepas J, Krzyżanowska-Kowalczyk J, Sieradzka M, Nowak P, Stochmal A, 2017. Clovamide and clovamide-rich extracts of three Trifolium species as antioxidants and moderate antiplatelet agents in vitro. Phytochem. 143:54-63. DOI: https://doi.org/10.1016/j.phytochem.2017.07.011
Kruidhof HM, Bastiaans L, Kropff MJ, 2009. Cover crop residue management for optimizing weed control. Plant Soil 318:169-84. DOI: https://doi.org/10.1007/s11104-008-9827-6
Lawley YE, Teasdale JR, Weil RR, 2012. The mechanism for weed suppression by a forage radish cover crop. Agron. J. 104:205-14. DOI: https://doi.org/10.2134/agronj2011.0128
Lou Y, Davis AS, Yannarell AC, 2016. Interactions between allelochemicals and the microbial community affect weed suppression following cover crop residue incorporation into soil. Plant Soil 399:357-71. DOI: https://doi.org/10.1007/s11104-015-2698-8
Macías FA, Castellano D, Molinillo JM, 2000. Search for a standard phytotoxic bioassay for allelochemicals. Selection of standard target species. J. Agric. Food Chem. 48:2512-21. DOI: https://doi.org/10.1021/jf9903051
Macías FA, Mejías FJ, Molinillo JM, 2019. Recent advances in allelopathy for weed control: from knowledge to applications. Pest Manage. Sci. 75:2413-36. DOI: https://doi.org/10.1002/ps.5355
Macías FA, Oliveros-Bastidas A, Marín D, Chinchilla N, Castellano D, Molinillo JM, 2014. Evidence for an allelopathic interaction between rye and wild oats. J. Agric. Food Chem. 62:9450-7. DOI: https://doi.org/10.1021/jf503840d
Maighany F, Khalghani J, Baghestani MA, Najafpour M, 2007. Allelopathic potential of Trifolium resupinatum L. (Persian clover) and Trifolium alexandrium L. (Berseem clover). Weed Biol. Manage. 7:178-83. DOI: https://doi.org/10.1111/j.1445-6664.2007.00250.x
Marchiosi R, dos Santos WD, Constantin RP, de Lima RB, Soares AR, Finger-Teixeira A, Rodrigues Mota T, de Oliveira DM, de Paiva Foletto-Felipe M, Abrahão J, Ferrarese-Filho O, 2020. Biosynthesis and metabolic actions of simple phenolic acids in plants. Phytochem. Rev. 19:865-906. DOI: https://doi.org/10.1007/s11101-020-09689-2
Mota FL, Queimada AJ, Pinho SP, Macedo EA, 2008. Aqueous solubility of some natural phenolic compounds. Ind. Eng. Chem. Res. 47:5182-9. DOI: https://doi.org/10.1021/ie071452o
Norsworthy JK, 2003. Allelopathic potential of wild radish (Raphanus raphanistrum. Weed Technol. 17:307-13. DOI: https://doi.org/10.1614/0890-037X(2003)017[0307:APOWRR]2.0.CO;2
Ohno T, Doolan KL, 2001. Effects of red clover decomposition on phytotoxicity to wild mustard seedling growth. Appl. Soil Ecol. 16:187-92. DOI: https://doi.org/10.1016/S0929-1393(00)00113-X
Oleszek W, Stochmal A, 2002. Triterpene saponins and flavonoids in the seeds of Trifolium species. Phytochem. 61:165-70. DOI: https://doi.org/10.1016/S0031-9422(02)00230-3
Oleszek W, Stochmal A, Janda B, 2007. Concentration of isoflavones and other phenolics in the aerial parts of Trifolium species. J. Agric. Food Chem. 55:8095-100. DOI: https://doi.org/10.1021/jf072024w
Olofsdotter M, Rebulanan M, Madrid A, Dali W, Navarez D, Olk DC, 2002. Why phenolic acids are unlikely primary allelochemicals in rice. J. Chem. Ecol. 28:229-42. DOI: https://doi.org/10.1023/A:1013531306670
Otte BA, Rice CP, Davis BW, Schomberg HH, Mirsky SB, Tully KL, 2020. Phenolic acids released to soil during cereal rye cover crop decomposition. Chemoecology 30:25-34. DOI: https://doi.org/10.1007/s00049-019-00295-z
Pardo-Muras M, Puig CG, Souto XC, Pedrol N, 2020. Water-soluble phenolic acids and flavonoids involved in the bioherbicidal potential of Ulex europaeus and Cytisus scoparius. S. Afr. J. Bot. 133:201-11. DOI: https://doi.org/10.1016/j.sajb.2020.07.023
Peillex C, Pelletier M, 2020. The impact and toxicity of glyphosate and glyphosate-based herbicides on health and immunity. J. Immunotoxicol. 17:163-74. DOI: https://doi.org/10.1080/1547691X.2020.1804492
Petit S, Cordeau S, Chauvel B, Bohan D, Guillemin JP, Steinberg C, 2018. Biodiversity-based options for arable weed management. A review. Agron. Sustainable Dev. 38:1-21. DOI: https://doi.org/10.1007/s13593-018-0525-3
Puig CG, Reigosa MJ, Valentão P, Andrade PB, Pedrol N, 2018. Unravelling the bioherbicide potential of Eucalyptus globulus Labill: Biochemistry and effects of its aqueous extract. PLoS One 13:e0192872. DOI: https://doi.org/10.1371/journal.pone.0192872
Price AJ, Stoll ME, Bergtold JS, Arriaga FJ, Balkcom KS, Kornecki TS, Raper RL, 2008. Effect of cover crop extracts on cotton and radish radicle elongation. Commun. Biom. Crop Sci. 3:60-6.
Qin B, Perry LG, Broeckling CD, Du J, Stermitz FR, Paschke MW, Vivanco JM, 2006. Phytotoxic allelochemicals from roots and root exudates of leafy spurge (Euphorbia esula L). Plant Signal. Behav. 1:323-7. DOI: https://doi.org/10.4161/psb.1.6.3563
Rakoczy‐Trojanowska M, Święcicka M, Bakera B, Kowalczyk M, Stochmal A, Bolibok L, 2020. Cocultivating rye with berseem clover affects benzoxazinoid production and expression of related genes. Crop Sci. 60:3228-46. DOI: https://doi.org/10.1002/csc2.20263
Reberg-Horton SC, Burton JD, Danehower DA, Ma G, Monks DW, Murphy JP, Ranells NN, Williamson JD, Creamer NG, 2005. Changes over time in the allelochemical content of ten cultivars of rye (Secale cereale L.). J. Chem. Ecol. 31:179-93. DOI: https://doi.org/10.1007/s10886-005-0983-3
Reigosa MJ, Pazos-Malvido E, 2007. Phytotoxic effects of 21 plant secondary metabolites on Arabidopsis thaliana germination and root growth. J. Chem. Ecol. 33:1456-66. DOI: https://doi.org/10.1007/s10886-007-9318-x
Reiss A, Fomsgaard IS, Mathiassen SK, Stuart RM, Kudsk P, 2018. Weed suppression by winter cereals: relative contribution of competition for resources and allelopathy. Chemoecology 28:109-21. DOI: https://doi.org/10.1007/s00049-018-0262-8
Ritz C, Baty F, Streibig JC, Gerhard D, 2015. Dose-response analysis using R. PLos One 10:e0146021. DOI: https://doi.org/10.1371/journal.pone.0146021
Scavo A, Restuccia A, Pandino G, Onofri A, Mauromicale G, 2018. Allelopathic effects of Cynara cardunculus L. leaf aqueous extracts on seed germination of some Mediterranean weed species. Ital. J. Agron. 13:119-25. DOI: https://doi.org/10.4081/ija.2018.1021
Schulz M, Marocco A, Tabaglio V, Macias FA, Molinillo JM, 2013. Benzoxazinoids in rye allelopathy-from discovery to application in sustainable weed control and organic farming. J. Chem. Ecol. 39:154-74. DOI: https://doi.org/10.1007/s10886-013-0235-x
Smith RG, Ryan MR, Menalled FD, 2011. Direct and indirect impacts of weed management practices on soil quality. In: J.L. Hatfield, T.J. Sauer (Ed.), Soil management: building a stable base for agriculture. ASA and SSSA, John Wiley and Sons, New York, NY, USA, pp. 275-286. DOI: https://doi.org/10.2136/2011.soilmanagement.c18
Souto XC, Bolaño JC, González L, Santos XX, 2001. HPLC Techniques-Phenolics. In: M.J. Reigosa (Ed.), Handbook of plant ecophysiology techniques. Kluwer Academic Publ., Netherlands, pp 251-282. DOI: https://doi.org/10.1007/0-306-48057-3_18
Sturm DJ, Kunz C, Gerhards R, 2016. Inhibitory effects of cover crop mulch on germination and growth of Stellaria media (L.) Vill., Chenopodium album L. and Matricaria chamomilla L. Crop Prot. 90:125-31. DOI: https://doi.org/10.1016/j.cropro.2016.08.032
Sturm DJ, Peteinatos G, Gerhards R, 2018. Contribution of allelopathic effects to the overall weed suppression by different cover crops. Weed Res. 58:331-7. DOI: https://doi.org/10.1111/wre.12316
Tabaglio V, Gavazzi C, Schulz M, Marocco A, 2008. Alternative weed control using the allelopathic effect of natural benzoxazinoids from rye mulch. Agron. Sustainable Dev. 28:397-401. DOI: https://doi.org/10.1051/agro:2008004
Tabaglio V, Marocco A, Schulz M, 2013. Allelopathic cover crop of rye for integrated weed control in sustainable agro-ecosystems. Ital. J. Agron. 8:e5. DOI: https://doi.org/10.4081/ija.2013.e5
Teasdale JR, 1996. Contribution of cover crops to weed management in sustainable agricultural systems. J. Prod. Agric. 9:475-9. DOI: https://doi.org/10.2134/jpa1996.0475
Teasdale JR, Rice CP, Cai G, Mangum RW, 2012. Expression of allelopathy in the soil environment: soil concentration and activity of benzoxazinoid compounds released by rye cover crop residue. Plant Ecol. 213:1893-905. DOI: https://doi.org/10.1007/s11258-012-0057-x
Tharayil N, Bhowmik PC, Xing B, 2008. Bioavailability of allelochemicals as affected by companion. J. Agric. Food Chem. 56:3706-13. DOI: https://doi.org/10.1021/jf073310a
Webster TM, Scully BT, Grey TL, Culpepper AS, 2013. Winter cover crops influence Amaranthus palmeri establishment. Crop Prot. 52:130-5. DOI: https://doi.org/10.1016/j.cropro.2013.05.015
Webster TM, Simmons DB, Culpepper AS, Grey TL, Bridges DC, Scully BT, 2016. Factors affecting potential for Palmer amaranth (Amaranthus palmeri) suppression by winter rye in Georgia, USA. Field Crops Res. 192:103-9. DOI: https://doi.org/10.1016/j.fcr.2016.04.020

How to Cite

Abou Chehade, L., Puig, C. G., Souto, C., Antichi, D., Mazzoncini, M., & Pedrol, N. (2021). Rye (<em>Secale cereale</em> L.) and squarrose clover (<em>Trifolium squarrosum</em> L.) cover crops can increase their allelopathic potential for weed control when used mixed as dead mulch. Italian Journal of Agronomy, 16(4). https://doi.org/10.4081/ija.2021.1869