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Hexazinone Resistance in Red Sorrel (Rumex acetosella)

Published online by Cambridge University Press:  20 January 2017

Zhenyi Li
Affiliation:
Department of Environmental Sciences, Dalhousie University Agricultural Campus
Nathan Boyd*
Affiliation:
Gulf Coast Research and Education Center, University of Florida
Nancy McLean
Affiliation:
Department of Animal and Plant Science, Dalhousie University Agricultural Campus, Truro, B2N 5E3, NS, Canada
Katherine Rutherford
Affiliation:
Department of Animal and Plant Science, Dalhousie University Agricultural Campus, Truro, B2N 5E3, NS, Canada
*
Corresponding author's E-mail: [email protected]

Abstract

Biannual applications of hexazinone have been applied in many lowbush blueberry fields in Nova Scotia for more than 30 years. Persistent reliance on a single herbicide chemistry may have selected for hexazinone-resistant red sorrel. The recommended rate of hexazinone (1.92 kg ai ha−1) no longer controls red sorrel in many growing regions. Six levels of hexazinone (0, 0.48, 0.96, 1.92, 3.84, and 7.68 kg ai ha−1) were applied to red sorrel plants grown in a greenhouse from seeds collected from three commercial fields and a no blueberry area to determine if they were hexazinone resistant. Red sorrel from two sites where hexazinone had not been applied regularly died at the 0.96 kg ai ha−1 rate of hexazinone whereas red sorrel from two commercial fields survived at 7.68 kg ai ha−1. It is concluded that red sorrel is hexazinone-resistant in some wild blueberry fields. A portion of the psbA gene was sequenced and it was determined that resistant plants had a Phe to Val substitution at position 255 in the D1 protein. This is the first recorded instance of hexazinone resistance in a perennial broadleaf weed in blueberry fields.

Type
Weed Management
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Bowes, J, Crofts, AR, Arntzen, CJ (1980) Redox reactions on the reducing side of photosystem II in chloroplast with altered herbicide binding properties. Arch Biochem Biophys 200:303308 Google Scholar
Cseh, A, Cernak, I, Taller, J (2009) Molecular characterization of atrazine resistance in common ragweed (Ambrosia artemisiifolia L.). J Appl Genet 50:321327 Google Scholar
Devine, MD, Duke, SO, Fedtke, C (1993) Phsiology of herbicide action. Englewood Cliffs, NJ Prentice-Hall Inc. 441 pGoogle Scholar
Devine, MD, Eberlein, CV (1997) Physiological, biochemical and molecular aspects of herbicide resistance based on altered target sites. Pages 159185 in Roe, RM, Burton, JD, Kuhr, RJ, eds. Herbicide activity: Toxicology, biochemistry and molecular biology. Amsterdam, The Netherlands IOS Google Scholar
Fuerst, EP, Norman, MA (1991) Interactions of herbicides with photosynthetic electron transport. Weed Sci 39:458464 Google Scholar
Fujifilm. No date. QuickGen Application Guide. http://www.kurabo.co.jp/bio/English/pdf/QuickGene_ap_en.pdf. Accessed: February 15, 2013Google Scholar
Gardner, G (1981) Azidoatrazine: Photoaffinity label for the site of triazine herbicide action in chloroplasts. Science 211:937940 Google Scholar
Gronwald, JW (1997) Resistance to photosystem II inhibiting herbicides. Pages 5359 in Prado, RD, Jorrín, J, García-Torres, L, eds. Weed and crop resistance to herbicides. Dordrecht, The Netherlands Kluwer Academic Publishers Google Scholar
Hall, TA (1999) BioEdit: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series 41:9598 Google Scholar
Hess, FD (2000) Light dependent herbicides: an overview. Weed Sci 48:160170 Google Scholar
Jia, X, Yuan, J, Shi, Y, Song, Y, Guoying, W, Wang, T, Li, Y (2007) A Ser-Gly substitution in plastid-encoded photosystem II D1 protein is responsible for atrazine resistance in foxtail millet (Setaria italica). Plant Growth Regul 52:8189 Google Scholar
Kennedy, KJ, Nams, VO, Boyd, NS (2010) Hexazinone and fertilizer impacts on red sorrel (Rumex acetosella) in wild blueberry. Weed Sci 58:317322 Google Scholar
Love, A (1983) The taxonomy of Acetosella. Berichte Der Schweizerischen Botanischen Gesellschaft = Bulletin de la Société Botanique Suisse 93:145168 Google Scholar
McCully, K, Jensen, K, Chiasson, G, Melanson, M (2005) Wild lowbush blueberry IPM weed management guide. New Brunswick Department of Agriculture, Fisheries, and Aquaculture. Kentville, Nova Scotia. http://www.gnb.ca/0171/10/017110020-e.pdf. Accessed: September 28, 2011Google Scholar
Perez-Jones, A, Mallory-Smith, C, Intanon, S (2009) Molecular analysis of hexazinone-resistant shepherd's-purse (Capsella bursa-pastoris) reveals a novel psbA mutation. Weed Sci 57:574578 Google Scholar
Seefeldt, SS, Jensen, JE, Furest, EP (1995) Log-logistic analysis of herbicide dose–response relationships. Weed Technol 9:218227 Google Scholar
Shukla, A, Devine, MD (2008) Basis of crop selectivity and weed resistance to triazine herbicides. Pages 111118 in LeBaron, HM, McFarland, JE, Burnside, OC, eds. The triazine herbicides: 50 years revolutionizing agriculture. San Diego, CA Elsevier Google Scholar
Tian, X, Darmency, H (2006) Rapid bidirectional allele-specific PCR identification for triazine resistance in higher plants. Pest Manag Sci 62:531536 Google Scholar
Trebst, A (1991) The molecular basis of plant resistance to photosystem II herbicides. Pages 145164 in Caseley, JC, Cussans, GW, Atkin, RK, eds. Herbicide resistance in weeds and crops. Oxford Butterworth-Heinemann Google Scholar
Trebst, A (1996) The molecular basis of plant resistance to photosystem II herbicides. Pages 4451 in Brown, TM, ed. Molecular genetics and evolution of pesticide resistance. Washington, DC American Chemical Society Google Scholar