Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-10T10:36:17.317Z Has data issue: false hasContentIssue false
  • English
  • Français

Resistance to bixlozone and clomazone in cross-resistant rigid ryegrass (Lolium rigidum) populations from southern Australia

Published online by Cambridge University Press:  28 January 2021

David J. Brunton Open the ORCID record for David J. Brunton [Opens in a new window] ,
Gurjeet Gill  and
Christopher Preston
David J. Brunton*
Affiliation:
Postgraduate Student, School of Agriculture Food and Wine, University of Adelaide, Glen Osmond, South Australia, Australia
Gurjeet Gill
Affiliation:
Associate Professor, School of Agriculture Food and Wine, University of Adelaide, Glen Osmond, South Australia, Australia
Christopher Preston
Affiliation:
Professor, School of Agriculture Food and Wine, University of Adelaide, Glen Osmond, South Australia, Australia
*
Author for correspondence: David J. Brunton, School of Agriculture Food and Wine, University of Adelaide, PMB 1, Glen Osmond, SA, Australia. (Email: david.brunton@adelaide.edu.au)
Get access Rights & Permissions [Opens in a new window]

Abstract

Three resistant (R) rigid ryegrass (Lolium rigidum Gaudin) populations from southern Australia (EP162, 375-14, and 198-15) with cross-resistance to thiocarbamate, chloroacetamide, and sulfonylisoxazoline herbicides displayed reduced sensitivity to the isoxazolidinone herbicides bixlozone and clomazone. Each of these R populations was exposed to two cycles of recurrent selection (RS) in which plants were treated with the field rate of bixlozone, survivors were bulk crossed, and seed was collected. After the first cycle of recurrent selection (RS1), the LD50 to bixlozone in population 198-15 increased to 17.5-fold compared with the S population and increased further to 26.9-fold after a second cycle of recurrent selection (RS2). The recurrent selection process also increased the level of resistance to bixlozone in populations EP162 and 375-14 (7.8- to 18.4-fold) compared with the S population. Phorate antagonized bixlozone and clomazone in SLR4 (34.6- and 28.1-fold increase in LD50) and both herbicides in populations EP162 (36.5- to 46.6-fold), 375-14 (71.4- to 73.9-fold), and 198-15 (86.4- to 91.5-fold) compared with the absence of phorate. The increase in LD50 of all L. rigidum RS populations when treated with phorate suggests a lack of herbicide activation is not the likely resistance mechanism to these herbicides. This research highlights the elevated risk of thiocarbamate-resistant L. rigidum populations to rapidly evolve resistance to the isoxazolidinone herbicides bixlozone and clomazone.

Keywords

Herbicide resistanceisoxazolidinonephoratemetabolic resistancerecurrent selection
Type
Research Article
Information
Weed Science , Volume 69 , Issue 3 , May 2021 , pp. 284 - 289
Check for updates
Copyright
© Weed Science Society of America, 2021

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

Associate Editor: Mithila Jugulam, Kansas State University

References

Beckie, HJ (2006) Herbicide-resistant weeds: management tactics and practices. Weed Technol 20:793–814 CrossRefGoogle Scholar
Beckie, HJ, Tardif, FJ (2012) Herbicide cross resistance in weeds. Crop Prot 35:15–28 CrossRefGoogle Scholar
Boutsalis, P, Gill, GS, Preston, C (2012) Incidence of herbicide resistance in rigid ryegrass (Lolium rigidum) across southeastern Australia. Weed Technol 26:391–398 CrossRefGoogle Scholar
Boutsalis, P, Gill, GS, Preston, C (2014) Control of rigid ryegrass in Australian wheat production with pyroxasulfone. Weed Technol 28:332–339 CrossRefGoogle Scholar
Broster, J, Pratley, J (2006) A decade of monitoring herbicide resistance in Lolium rigidum in Australia. Anim Prod Sci 46:1151–1160 CrossRefGoogle Scholar
Brunton, DJ, Boutsalis, P, Gill, G, Preston, C (2018) Resistance to multiple PRE herbicides in a field-evolved rigid ryegrass (Lolium rigidum) population. Weed Sci 66:581–585 CrossRefGoogle Scholar
Brunton, DJ, Boutsalis, P, Gill, G, Preston, C (2019) Resistance to very-long-chain fatty-acid (VLCFA)-inhibiting herbicides in multiple field-selected rigid ryegrass (Lolium rigidum) populations. Weed Sci 67:267–272 CrossRefGoogle Scholar
Brunton, DJ, Boutsalis, P, Gill, G, Preston, C (2020a) Control of thiocarbamate-resistant rigid ryegrass (Lolium rigidum) in wheat in southern Australia. Weed Technol 34:19–24 CrossRefGoogle Scholar
Brunton, DJ, Boutsalis, P, Gill, G, Preston, C (2020b) Varying responses of field-selected herbicide-resistant rigid ryegrass (Lolium rigidum) populations to combinations of phorate with PPI herbicides. Weed Sci 68:367–372 CrossRefGoogle Scholar
Busi, R, Gaines, TA, Powles, S (2017) Phorate can reverse P450 metabolism-based herbicide resistance in Lolium rigidum . Pest Manag Sci 73:410–417 CrossRefGoogle ScholarPubMed
Busi, R, Gaines, TA, Walsh, MJ, Powles, SB (2012) Understanding the potential for resistance evolution to the new herbicide pyroxasulfone: field selection at high doses versus recurrent selection at low doses. Weed Res 52:489–499 CrossRefGoogle Scholar
Busi, R, Powles, SB (2013) Cross-resistance to prosulfocarb and triallate in pyroxasulfone-resistant Lolium rigidum. Pest Manag Sci 69:1379–1384 CrossRefGoogle ScholarPubMed
Busi, R, Powles, SB (2016) Cross-resistance to prosulfocarb plus S-metolachlor and pyroxasulfone selected by either herbicide in Lolium rigidum . Pest Manag Sci 72:1664–1672 CrossRefGoogle Scholar
Casida, JE, Gray, RA, Tilles, H (1974) Thiocarbamate sulfoxides: potent, selective, and biodegradable herbicides. Science 184:573–574 Google ScholarPubMed
Culpepper, AS, York, AC, Marth, JL, Corbin, FT (2001) Effect of insecticides on clomazone absorption, translocation, and metabolism in cotton. Weed Sci 49:613–616 CrossRefGoogle Scholar
Dücker, R, Lorentz, L, Hull, R, Anderson, M, Moss, S, Beffa, R (2016) Discovering the mechanism of enhanced metabolism in flufenacet resistant grass weeds. Julius-Kühn-Archiv 452:35–41 Google Scholar
Durst, F, Salaun, JP, WerckReichhart, D, Zimmerlin, F (1997) Cytochrome P450 endowed herbicide metabolism. Pages 101–108 in DePrado, R, Jorrin, J, GarciaTorres, L, eds. Weed and Crop Resistance to Herbicides. Dordrecht: Kluwer Academic CrossRefGoogle Scholar
ElNaggar, SF, Creekmore, RW, Schocken, MJ, Rosen, RT, Robinson, RA (1992) Metabolism of clomazone herbicide in soybean. J Agric Food Chem 40:880–883 CrossRefGoogle Scholar
Ferhatoglu, Y, Avdiushko, S, Barrett, M (2005) The basis for the safening of clomazone by phorate insecticide in cotton and inhibitors of cytochrome P450s. Pest Biochem Physiol 81:59–70 CrossRefGoogle Scholar
Ferhatoglu, Y, Barrett, M (2006) Studies of clomazone mode of action. Pest Biochem Physiol 85:7–14 CrossRefGoogle Scholar
Fuerst, EP (1987) Understanding the mode of action of the chloroacetamide and thiocarbamate herbicides. Weed Technol 1:270–277 CrossRefGoogle Scholar
Guo, F, Iwakami, S, Yamaguchi, T, Uchino, A, Sunohara, Y, Matsumoto, H (2019) Role of CYP81A cytochrome P450s in clomazone metabolism in Echinochloa phyllopogon . Plant Sci 283:321–328 CrossRefGoogle ScholarPubMed
Hall, LM, Tardif, FJ, Powles, SB (1994) Mechanisms of cross and multiple herbicide resistance in Alopecurus-myosuroides and Lolium-rigidum . Phytoprotection 75:17–23 CrossRefGoogle Scholar
Kern, AJ, Peterson, DM, Miller, EK, Colliver, CC, Dyer, WE (1996) Triallate resistance in Avena fatua L. is due to reduced herbicide activation. Pest Biochem Physiol 56:163–173 CrossRefGoogle Scholar
Keshtkar, E, Mathiassen, SK, Moss, SR, Kudsk, P (2015) Resistance profile of herbicide-resistant Alopecurus myosuroides (black-grass) populations in Denmark. Crop Prot 69:83–89 CrossRefGoogle Scholar
Mangin, AR, Hall, LM, Beckie, HJ (2016) Triallate-resistant wild oat (Avena fatua L.): unexpected resistance to pyroxasulfone and sulfentrazone. Can J Plant Sci 97:20–25 Google Scholar
Norman, MA, Liebl, RA, Widholm, JM (1990) Uptake and metabolism of clomazone in tolerant-soybean and susceptible-cotton photomixotrophic cell suspension cultures. Plant Physiol 92:777–784 Google ScholarPubMed
Preston, C, Tardif, FJ, Christopher, JT, Powles, SB (1996) Multiple resistance to dissimilar herbicide chemistries in a biotype of Lolium rigidum due to enhanced activity of several herbicide degrading enzymes. Pest Biochem Physiol 54:123–134 CrossRefGoogle Scholar
Ritz, C, Kniss, AR, Streibig, JC (2015) Research methods in weed science: statistics. Weed Sci 63:166–187 CrossRefGoogle Scholar
Seefeldt, SS, Jensen, JE, Fuerst, EP (1995) Log-logistic analysis of herbicide dose-response relationships. Weed Technol 9:218–227 CrossRefGoogle Scholar
Siminszky, B (2006) Plant cytochrome P450-mediated herbicide metabolism. Phytochem Rev 5:445–458 CrossRefGoogle Scholar
Tardif, FJ, Powles, SB (1999) Effect of malathion on resistance to soil-applied herbicides in a population of rigid ryegrass (Lolium rigidum). Weed Sci 47:258–261 CrossRefGoogle Scholar
Weimer, MR, Buhler, DH, Balke, NE (1991) Investigation of the selectivity mechanism of plants to the herbicide, clomazone. Pages 486–487 in Caseley, JC, Cussans, GW, Atkin, RK, eds. Herbicide Resistance in Weeds and Crops. Oxford: Butterworth-Heinemann CrossRefGoogle Scholar
Yasuor, H, TenBrook, PL, Tjeerdema, RS, Fischer, AJ (2008) Responses to clomazone and 5-ketoclomazone by Echinochloa phyllopogon resistant to multiple herbicides in Californian rice fields. Pest Manag Sci 64:1031–1039 CrossRefGoogle ScholarPubMed
Yasuor, H, Zou, W, Tolstikov, VV, Tjeerdema, RS, Fischer, AJ (2010) Differential oxidative metabolism and 5-ketoclomazone accumulation are involved in Echinochloa phyllopogon resistance to clomazone. Plant Physiol 153:319–326 CrossRefGoogle ScholarPubMed
Yu, Q, Powles, S (2014) Metabolism-based herbicide resistance and cross-resistance in crop weeds: A threat to herbicide sustainability and global crop production. Plant Physiol 166:1106–1118 CrossRefGoogle ScholarPubMed
Yuan, JS, Tranel, PJ, Stewart, CN (2007) Non-target-site herbicide resistance: a family business. Trends Plant Sci 12:6–13 CrossRefGoogle ScholarPubMed