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Variation in Response and Resistance to Glyphosate and Glufosinate in California Populations of Italian Ryegrass (Lolium perenne ssp. multiflorum)

Published online by Cambridge University Press:  14 December 2017

Elizabeth Karn
Affiliation:
Graduate Student and Professor, Department of Plant Sciences MS4, University of California–Davis, Davis, CA 95616
Roland Beffa
Affiliation:
Bayer AG, Division CropScience, Weed Resistance Research, 65926 Frankfurt am Main, Germany
Marie Jasieniuk*
Affiliation:
Graduate Student and Professor, Department of Plant Sciences MS4, University of California–Davis, Davis, CA 95616
*
*Corresponding author’s E-mail: [email protected]

Abstract

Reduced control of Italian ryegrass in California with herbicides has raised concerns about the evolution of populations with resistance to multiple herbicides. The goal of this study was to investigate variation among populations in plant response and resistance to glyphosate and glufosinate in Italian ryegrass from vineyards and orchards in northwest California. Population resistance screening using field-collected seed revealed up to 56.9% of individuals surviving glyphosate treatment at 1,678 g ae ha−1, and 53.5% of individuals surviving glufosinate treatment at 2,242 g ai ha−1 in the same population. Frequencies of surviving plants within populations varied among screening times, particularly for glufosinate. Treating vegetatively propagated, genetically identical tillers with each herbicide pointed to separate mechanisms of resistance rather than cross-resistance to glyphosate and glufosinate. Dose–response experiments were conducted for each herbicide at two different screening times using a subset of populations, field-collected seed, and 10 herbicide rates. Plant survival and biomass were evaluated for each population at 3 wk after treatment and for plant regrowth 1 wk thereafter. Log-logistic regression models fit to the data were used to estimate LD50, GR50, and RD50 values and calculate resistance indices (R/S ratios). Based on LD50 values, the most highly resistant population was 14.4- to 19.2-fold more resistant to glyphosate than the most susceptible population tested but only 1.6- to 2.0-fold more resistant to glufosinate than the most susceptible population tested. Levels of resistance to both herbicides varied with screening time period and variable measured. Results indicate high frequencies of glyphosate-resistant plants but an early stage in the evolution of glufosinate resistance in some Italian ryegrass populations of northwest California.

Type
Weed Biology and Ecology
Copyright
© Weed Science Society of America, 2017 

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Footnotes

Associate Editor for this paper: Muthukumar V. Bagavathiannan, Texas A&M University.

References

Literature Cited

Avila-Garcia, WV, Mallory-Smith, C (2011) Glyphosate-resistant Italian ryegrass (Lolium perenne) populations also exhibit resistance to glufosinate. Weed Sci 59:305309 CrossRefGoogle Scholar
Avila-Garcia, WV, Sanchez-Olguin, E, Hulting, AG, Mallory-Smith, C (2012) Target-site mutation associated with glufosinate resistance in Italian ryegrass (Lolium perenne L. ssp. multiflorum). Pest Manag Sci 68:12481254 CrossRefGoogle ScholarPubMed
Balfourier, F, Charmet, G, Ravel, C (1998) Genetic differentiation within and between natural populations of perennial and annual ryegrass (Lolium perenne and L. rigidum). Heredity 81:100110 CrossRefGoogle Scholar
Boutsalis, P (2001) Syngenta Quick-Test: a rapid whole plant test for herbicide resistance. Weed Technol 15:257263 CrossRefGoogle Scholar
Busi, R, Powles, SB (2009) Evolution of glyphosate resistance in a Lolium rigidum population by glyphosate selection at sublethal doses. Heredity 103:318325 CrossRefGoogle Scholar
Busi, R, Yu, Q, Barrett-Lennard, R, Powles, SB (2008) Long distance pollen-mediated flow of resistance genes in Lolium rigidum . Theor Appl Genet 117:12811290 CrossRefGoogle ScholarPubMed
Coetzer, E, Al-Khatib, K, Loughlin, TM (2001) Glufosinate efficacy, absorption, and translocation in amaranth as affected by relative humidity and temperature. Weed Sci 49:813 CrossRefGoogle Scholar
Délye, C, Boucansaud, K, Pernin, F, Le Corre, V (2009) Variation in the gene encoding acetolactate-synthase in Lolium species and proactive detection of mutant, herbicide-resistant alleles. Weed Res 49:326336 CrossRefGoogle Scholar
Délye, C, Jasieniuk, M, Le Corre, V (2013) Deciphering the evolution of herbicide resistance in weeds. Trends Genet 29:649658 CrossRefGoogle ScholarPubMed
Gaines, TA, Lorentz, L, Figge, A, Hermann, J, Maiwald, F, Ott, MC, Han, H, Busi, R, Yu, Q, Powles, SB, Beffa, R (2014) RNA-Seq transcriptome analysis to identify genes involved in metabolism-based diclofop resistance in Lolium rigidum . Plant J 78:865876 CrossRefGoogle ScholarPubMed
Ge, X, d’Avignon, DA, Ackerman, JJH, Collavo, A, Sattin, M, Ostrander, EL, Hall, EL, Sammons, RD (2012) Vacuolar glyphosate sequestration correlates with glyphosate resistance in ryegrass (Lolium ssp.) from Australia, South America, and Europe: a 31P NMR investigation. J Agric Food Chem 60:12431250 CrossRefGoogle Scholar
Ge, X, d’Avignon, DA, Ackerman, JJH, Duncan, B, Spaur, MB, Sammons, RD (2011) Glyphosate-resistant horseweed made sensitive to glyphosate: low-temperature suppression of glyphosate vacuolar sequestration revealed by 31P NMR. Pest Manag Sci 67:12151221 CrossRefGoogle Scholar
Ghanizadeh, H, Harrington, KC, James, TK (2015) Glyphosate-resistant Lolium multiflorum and Lolium perenne populations from New Zealand are also resistant to glufosinate and amitrole. Crop Prot 78:14 CrossRefGoogle Scholar
Heap, I (2017). International Survey of Herbicide Resistant Weeds. http://weedscience.org. Accessed: March 22, 2017Google Scholar
Jalaludin, A, Ngim, J, Baki, BB, Zazali, A (2010) Preliminary findings of potentially resistant goosegrass (Eleusine indica) to glufosinate-ammonium in Malaysia. Weed Biol Manag 10:256260 CrossRefGoogle Scholar
Jalaludin, A, Yu, Q, Powles, SB (2015) Multiple resistance across glufosinate, glyphosate, paraquat, and ACCase-inhibiting herbicides in an Eleusine indica population. Weed Res 55:8289 CrossRefGoogle Scholar
Jalaludin, A, Yu, Q, Zoellner, P, Beffa, R, Powles, SB (2017) Characterisation of glufosinate resistance mechanisms in Eleusine indica . Pest Manag Sci 73:10911100 CrossRefGoogle ScholarPubMed
Jasieniuk, M, Ahmad, R, Sherwood, AM, Firestone, JL, Perez-Jones, A, Lanini, WT, Mallory-Smith, C, Stednick, Z (2008) Glyphosate-resistant Italian ryegrass (Lolium multiflorum) in California: distribution, response to glyphosate, and molecular evidence for an altered target enzyme. Weed Sci 56:496502 CrossRefGoogle Scholar
Jasieniuk, M, Brule-Babel, AL, Morrison, IN (1996) The evolution and genetics of herbicide resistance in weeds. Weed Sci 44:176193 CrossRefGoogle Scholar
Karn, E, Jasieniuk, M (2017) Nucleotide diversity at site 106 of EPSPS in Lolium perenne L. ssp. multiflorum from California indicates multiple evolutionary origins of herbicide resistance. Front Plant Sci 8:777 CrossRefGoogle ScholarPubMed
Knezevic, SV, Streibig, JC, Ritz, C (2007) Utilizing R software package for dose response studies: the concept and data analysis. Weed Technol 21:840848 CrossRefGoogle Scholar
Kumaratilake, AR, Preston, C (2005) Low temperature reduces glufosinate activity and translocation in wild radish (Raphanus raphanistrum). Weed Sci 56:1016 CrossRefGoogle Scholar
Kurata, K, Ichihara, M, Ishida, Y, Shimono, Y, Tominaga, T (2017) Glufosinate-resistant Italian ryegrass populations emerge from glyphosate-resistant populations in Japan. Int Inv J Agric. Soil Sci 5:2125 Google Scholar
Moretti, ML, Hanson, BD, Hembree, KJ, Shrestha, A (2013) Glyphosate resistance is more variable than paraquat resistance in a multiple-resistant hairy fleabane (Conyza bonariensis) population. Weed Sci 61:396402 CrossRefGoogle Scholar
Neve, P, Powles, SB (2005) High survival frequencies at low herbicide use rates in populations of Lolium rigidum result in rapid evolution of herbicide resistance. Heredity 95:485492 CrossRefGoogle ScholarPubMed
Neve, P, Vila-Aiub, M, Roux, F (2009) Evolutionary thinking in agricultural weed management. New Phytol 184:783793 CrossRefGoogle ScholarPubMed
Perez-Jones, A, Park, KW, Polge, N, Colquhoun, J, Mallory-Smith, CA (2007) Investigating the mechanisms of glyphosate resistance in Lolium multiflorum . Planta 226:395404 CrossRefGoogle ScholarPubMed
Pimentel, D, Zuniga, R, Morrison, D (2005) Update on the environmental and economic costs associated with alien-invasive species in the United States. Ecol Econ 52:273288 CrossRefGoogle Scholar
Pline, WA, Wu, J, Hatzios, KK (1999) Effects of temperature and chemical additives on the response of transgenic herbicide-resistant soybeans to glufosinate and glyphosate applications. Pestic Biochem Physiol 65:119131 CrossRefGoogle Scholar
Powles, SB (2008) Evolved glyphosate-resistant weeds around the world: lessons to be learnt. Pest Manag Sci 64:360365 CrossRefGoogle ScholarPubMed
Powles, SB, Lorraine-Colwill, DF, Dellow, JJ, Preston, C (1998) Evolved resistance to glyphosate in rigid ryegrass (Lolium rigidum) in Australia. Weed Sci 46:604607 CrossRefGoogle Scholar
Powles, SB, Yu, Q (2010) Evolution in action: plants resistant to herbicides. Annu Rev Plant Biol 61:317347 CrossRefGoogle ScholarPubMed
Preston, C, Wakelin, AM, Dolman, FC, Bostamam, Y, Boutsalis, P (2009) A decade of glyphosate-resistant Lolium around the world: mechanisms, genes, fitness, and agronomic management. Weed Sci 57:435441 CrossRefGoogle Scholar
R Core Team (2013) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. http://www.R-project.org/ Google Scholar
Ramsay, RJ, Stephenson, GR, Hall, JC (2002) Effect of relative humidity on the uptake, translocation, and efficacy of glufosinate ammonium in wild oat (Avena fatua). Pestic Biochem Physiol 73:18 CrossRefGoogle Scholar
Salas, RA, Dayan, FE, Pan, Z, Watson, SB, Dickson, JW, Scott, RC, Burgos, NR (2012) EPSPS gene amplification in glyphosate-resistant Italian ryegrass (Lolium perenne ssp. multiflorum) from Arkansas. Pest Manag Sci 68:12231230 CrossRefGoogle ScholarPubMed
Sellers, BA, Smeda, RJ, Li, J (2003) Glutamine synthetase activity and ammonium accumulation is influenced by time of glufosinate application. Pestic Biochem Physiol 78:920 CrossRefGoogle Scholar
Seng, CT, Lun, LV, San, CT, Sahid, IB (2010) Initial report of glufosinate and paraquat multiple resistance that evolved in a biotype of goosegrass (Eleusine indica) in Malaysia. Weed Biol Manag 10:229233 CrossRefGoogle Scholar
Sharma, SD, Singh, M (2001) Environmental factors affecting absorption and bio-efficacy of glyphosate in Florida beggarweed (Desmodium tortuosum). Crop Prot 20:511516 CrossRefGoogle Scholar
Simarmata, M, Kaufmann, JE, Penner, D (2003) Potential basis of glyphosate resistance in California rigid ryegrass (Lolium rigidum). Weed Sci 51:678682 CrossRefGoogle Scholar
Steckel, GJ, Hart, SE, Wax, LM (1997) Absorption and translocation of glufosinate on four weed species. Weed Sci 45:378381 CrossRefGoogle Scholar
Wakelin, AM, Lorraine-Colwill, DM, Preston, C (2004) Glyphosate resistance in four different populations of Lolium rigidum is associated with reduced translocation of glyphosate to meristematic zones. Weed Res 44:453459 CrossRefGoogle Scholar
Waltz, AL, Martin, AR, Roeth, FW, Lindquist, JL (2004) Glyphosate efficacy on velvetleaf varies with application time of day. Weed Technol 18:931939 CrossRefGoogle Scholar