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Ozone Enhances Adaptive Benefit of Glyphosate Resistance in Horseweed (Conyza canadensis)

Published online by Cambridge University Press:  20 January 2017

D. A. Grantz ,
A. Shrestha  and
H-B. Vu
D. A. Grantz*
Affiliation:
Department of Botany and Plant Sciences and Air Pollution Research Center, University of California, Riverside, CA, and Kearney Agricultural Center, Parlier, CA 93648
A. Shrestha
Affiliation:
Statewide Integrated Pest Management Program, Kearney Agricultural Center, University of California, Parlier, CA 93648
H-B. Vu
Affiliation:
Department of Botany and Plant Sciences and Air Pollution Research Center, University of California, Riverside, CA, and Kearney Agricultural Center, Parlier, CA 93648
*
Corresponding author's E-mail: [email protected]
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Abstract

Since the first identification of glyphosate resistance in horseweed in California in 2005, the glyphosate-sensitive (GS) biotype has become rare, whereas the glyphosate-resistant (GR) biotype has become dominant in the eastern San Joaquin Valley (SJV). This is an area exposed to regular usage of glyphosate and to high levels of ambient ground-level ozone (O3). A previous study showed that SJV biotypes of GR are more robust than GS in the absence of ozone. This advantage was reduced, though not eliminated, at elevated O3. This suggests that the rapid evolution of resistance to glyphosate was not linked to evolution of resistance to O3. In this study, we contrasted these responses to O3 in the presence of concurrent glyphosate pressure. The GR and GS biotypes differed in growth and injury, reflecting their known differential sensitivities to glyphosate, but responded similarly to O3 with no O3 × biotype interaction. Ozone imposed an unexpected, but ecologically important, impact that enhanced the performance advantage of GR over GS. In the presence of the combination of glyphosate and O3 the biomass of GR was reduced to low but viable levels, whereas the biomass of GS was reduced to nonviable levels that effectively removed it from the population. These data do not support a genetic linkage between resistance to glyphosate and to O3, but suggest that air pollution may have accelerated the fixation of glyphosate-resistance alleles in California horseweed populations.

Keywords

Glyphosatehorseweed, Conyza canadensis (L.) Cronq. ERICAOzoneO3herbicide resistancerapid evolution
Type
Weed Biology and Ecology
Information
Weed Science , Volume 56 , Issue 4 , August 2008 , pp. 549 - 554
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Alcorta, M., Shrestha, A., Fidelibus, M., and Hembree, K. J. 2007. Growth and phenology of two different horseweed (Conyza canadensis) biotypes are influenced by shade in a vineyard. Abstract No. 78 in Weed Science Society of America Annual Meeting, San Antonio, TX.Google Scholar
Andersen, C. P. 2003. Source–sink balance and carbon allocation below ground in plants exposed to ozone. New Phytol. 157:213–228.CrossRefGoogle ScholarPubMed
Baucom, R. S. and Mauricio, R. 2004. Fitness costs and benefits of novel herbicide tolerance in a noxious weed. Proc. Natl. Acad. Sci. USA. 101:13,386–13,390.CrossRefGoogle Scholar
Buhler, D. D. 1992. Population dynamics and control of annual weeds in corn (Zea mays) as influenced by tillage systems. Weed Sci. 40:241–248.CrossRefGoogle Scholar
California Air Resources Board (CARB) 2007. The best and worst ozone air quality in California. http://www.arb.ca.gov/aqd/aqfaq/ozonedot.html.Google Scholar
California Department of Pesticide Regulation (CDPR) 2006. Pesticide Use Reporting—2006 Summary Data. http://www.cdpr.ca.gov/docs/pur/pur06rep/top100_ais.pdf.Google Scholar
Clements, D. R., DiTommaso, A., Jordan, N., Booth, B. D., Cardina, J., Doohan, D., Mohler, C. L., Murphy, S. D., and Swanton, C. J. 2004. Adaptability of plants invading North American cropland. Agric. Ecosyst. Environ. 104:379–398.CrossRefGoogle Scholar
Collins, W. J., Stevenson, D. S., Johnson, C. E., and Derwent, R. G. 2000. The European regional ozone distribution and its links with the global scale for the years 1992 and 2015. Atmos. Environ. 34:255–267.CrossRefGoogle Scholar
Cooley, D. R. and Manning, W. J. 1987. The impact of ozone on assimilate partitioning in plants: a review. Environ. Pollut. 47:95–113.CrossRefGoogle ScholarPubMed
Dauer, J. T., Mortensen, D. A., and VanGessel, M. J. 2007. Temporal and spatial dynamics of long-distance Conyza canadensis seed dispersal. J. Appl. Ecol. 44:105–114.CrossRefGoogle Scholar
Flagler, R. B. 1998. Recognition of air pollution injury to vegetation: A pictorial atlas. Pittsburgh, PA Air Waste Management Association.Google Scholar
Fuhrer, J. and Booker, F. 2003. Ecological issues of ozone: agricultural issues. Environ. Int. 29:141–154.CrossRefGoogle ScholarPubMed
Glater, R. A., Solberg, R. A., and Scott, F. M. 1962. A developmental study of the leaves of Nicotiana glutinosa as related to their smog sensitivity. Am. J. Bot. 49:954–970.Google Scholar
Grantz, D. A. 2003. Ozone impacts on cotton: towards an integrated mechanism. Environ. Pollut. 126:331–344.CrossRefGoogle ScholarPubMed
Grantz, D. A. and Farrar, J. F. 2000. Ozone inhibits phloem loading from a transport pool: compartmental efflux analysis in Pima cotton. Austr. J. Plant Physiol. 27:859–868.Google Scholar
Grantz, D. A., Gunn, S., and Vu, H. B. 2006. Ozone impacts on plant development: a meta-analysis of root/shoot allocation and growth. Plant Cell Environ. 29:1193–1209.CrossRefGoogle ScholarPubMed
Grantz, D. A., Shrestha, A., and Vu, H. 2008. Early vigor and ozone response in horseweed (Conyza canadensis) biotypes differing in glyphosate resistance. Weed Sci. 56:224–230.CrossRefGoogle Scholar
Grantz, D. A., Silva, V., Toyota, M., and Ott, N. 2003. Ozone increases root respiration but decreases leaf CO2 assimilation in cotton and melon. J. Exp. Bot. 43:2375–2384.CrossRefGoogle Scholar
Grantz, D. A. and Yang, S. 1996. Effects of O3 on hydraulic architecture in Pima cotton—biomass allocation and water transport capacity of roots and shoots. Plant Physiol. 112:1649–1657.CrossRefGoogle Scholar
Hanson, B. D., Shrestha, A., Pelham, C., and Shaner, D. L. 2007. An enzyme assay and GIS as tools to characterize and determine the spatial distribution of glyphosate-resistant horseweed in the San Joaquin Valley of California. Abstract No. 268 in Weed Science Society of America Annual Meeting, San Antonio, TX.Google Scholar
Heap, I. M. 1997. The occurrence of herbicide-resistant weeds worldwide. Pesticide Sci. 51:235–243.3.0.CO;2-N>CrossRefGoogle Scholar
Heap, I. M. 2008. International Survey of Herbicide Resistant Weeds. www.weedscience.org.Google Scholar
Heck, W. W., Philbeck, R. B., and Denning, J. A. 1978. A continuous stirred tank reactor (CSTR) system for exposing plants to gaseous air pollutants. Publication No. ARS-5-181. Washington, DC U.S. Department of Agriculture.Google Scholar
Hendry, A. P., Farrugia, T. J., and Kinnison, M. T. 2008. Human influences on rates of phenotypic change in wild animal populations. Mol. Ecol. 17:20–29.CrossRefGoogle ScholarPubMed
Holm, L. J., Doll, E., Holm, P. J., and Herberger, J. 1997. in. World Weeds: Natural Histories and Distribution. New York John Wiley & Sons. 226–235.Google Scholar
Koger, C. H., Poston, D. H., Hayes, R. M., and Montgomery, R. F. 2004. Glyphosate-resistant horseweed (Conyza canadensis) in Mississippi. Weed Technol. 18:820–825.CrossRefGoogle Scholar
Koger, C. H., Shaner, D. L., Henry, W. B., Nadler-Hassar, T., Thomas, W. E., and Wilcut, J. W. 2005. Assessment of two nondestructive assays for detecting glyphosate resistance in horseweed (Conyza canadensis). Weed Sci. 53:559–566.CrossRefGoogle Scholar
Mortensen, L. K. and Engvild, C. 1995. Effects of ozone on 14C translocation velocity and growth of spring wheat (Triticum aestivum L.) exposed in open-top chambers. Environ. Pollut. 87:135–140.CrossRefGoogle ScholarPubMed
Muller, M., Kohle, B., Tausz, M., Grill, D., and Lutz, C. 1996. The assessment of ozone stress by recording chromosomal aberrations in root tips of spruce trees (Picea abies (L.) Karst). J. Plant Physiol. 148:160–165.CrossRefGoogle Scholar
Nandula, V. K., Eubank, T. W., Poston, D. H., Koger, C. H., and Reddy, K. N. 2006. Factors affecting germination of horseweed (Conyza canadensis). Weed Sci. 54:898–902.CrossRefGoogle Scholar
Reiling, K. and Davison, A. W. 1992. Spatial variation in ozone resistance of British populations of Plantago major L. New Phytol. 122:699–708.CrossRefGoogle Scholar
Rennenberg, H., Herschbach, C., and Polle, A. 1996. Consequences of air pollution on shoot–root interactions. J. Plant Physiol. 148:296–301.CrossRefGoogle Scholar
Shrestha, A., Hembree, K. J., and Va, N. 2007. Growth stage influences level of resistance in glyphosate-resistant horseweed. Calif. Agric. 61:67–70.CrossRefGoogle Scholar
Taylor, G. E. Jr., Pitelka, L. F., and Clegg, M. T. 1991. Ecological Genetics and Air Pollution Stress. Pages 1–9. in Taylor, G. E. Jr., Pitelka, L. F., and Clegg, M. T. New York Springer-Verlag.CrossRefGoogle Scholar
Thébaud, C., Finzi, A. C., Affre, L., Debussche, M., and Escarre, J. 1996. Assessing why two introduced Conyza differ in their ability to invade Mediterranean old fields. Ecology. 77:791–804.CrossRefGoogle Scholar
Ting, I. P. and Dugger, W. M. 1971. Ozone resistance in tobacco plants: A possible relationship to water balance. Atmos. Environ. 5:147–150.CrossRefGoogle Scholar
Tingey, D. T., Reinert, R. A., Dunning, J. A., and Heck, W. W. 1971. Vegetation injury from the interaction of nitrogen dioxide and sulfur dioxide. Phytopathology. 61:1506–1511.CrossRefGoogle Scholar
Van Gessel, M. J. 2001. Glyphosate-resistant horseweed from Delaware. Weed Sci. 49:703–705.CrossRefGoogle Scholar
Wonisch, A., Muller, M., Tausz, M., Soja, G., and Grill, D. 1999. Simultaneous analyses of chromosomes in root meristems and of the biochemical status of needle tissues of three different clones of Norway spruce trees challenged with moderate ozone levels. Eur. J. For. Pathol. 29:281–294.CrossRefGoogle Scholar