Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-18T08:29:28.844Z Has data issue: false hasContentIssue false

Enhanced sensitivity to cloransulam-methyl in imidazolinone-resistant smooth pigweed

Published online by Cambridge University Press:  20 January 2017

Jingrui Wu
Affiliation:
Virginia Polytechnic Institute and State University, Blacksburg, VA 24061
Kriton K. Hatzios
Affiliation:
Virginia Polytechnic Institute and State University, Blacksburg, VA 24061
Henry P. Wilson
Affiliation:
Eastern Shore Agricultural Research and Extension Center, Virginia Polytechnic Institute and State University, Painter, VA 23420

Abstract

Several populations of smooth pigweed with resistance to imidazolinone (IMI) herbicides have been identified in recent years. One IMI-resistant population (R2) was 10-fold more sensitive to cloransulam-methyl in the greenhouse when compared with a susceptible (S) population. Laboratory studies were conducted to determine if differences in the absorption, translocation, and metabolism of cloransulam-methyl existed between S and R2 populations and to determine if these differences could account for the whole-plant responses observed in the greenhouse. Enzyme assays were also conducted to determine if differences in acetolactate synthase (ALS) sensitivity to cloransulam-methyl existed between S and R2 populations. Absorption of foliar-applied cloransulam-methyl was rapid and similar in both populations of smooth pigweed. Translocation of the absorbed radioactivity out of the treated leaf was symplastic and generally similar in both populations. Translocated radioactivity was detected primarily in shoots above and below the treated leaf with little movement to the roots. 14C-cloransulam-methyl metabolism was also similar in S and R2 populations. Differential tolerance to cloransulam-methyl in S and R2 populations in the greenhouse cannot be explained by differences in the absorption, translocation, and metabolism of this herbicide. However, ALS from R2 was 25-fold more sensitive to inhibition by cloransulam-methyl than ALS from S.

Type
Research Article
Copyright
Copyright © Weed Science Society of America 

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.)

References

Literature Cited

Ackley, J. A., Hatzios, K. K., and Wilson, H. P. 1999. Absorption, translocation, and metabolism of rimsulfuron in black nightshade (Solanum nigrum), Eastern black nightshade (Solanum ptycanthum), and hairy nightshade (Solanum sarrachoides). Weed Technol. 13:151156.CrossRefGoogle Scholar
Chaleff, R. S. and Mauvais, C. J. 1984. Acetolactate synthase is the site of action of two sulfonylurea herbicides in higher plants. Science 224:1,4431,445.Google Scholar
Chism, W. J., Birch, J. B., and Bingham, S. W. 1992. Nonlinear regressions for analyzing growth stage and quinclorac interactions. Weed Technol. 6:898903.Google Scholar
Dorich, R. A. and Schultz, M. E. 1997. Firstrate herbicide: a new broadleaf herbicide for soybeans. Down Earth 52:110.Google Scholar
Foes, M. J., Lixin, L., Tranel, P. J., Wax, L. M., and Stoller, E. W. 1998. A biotype of common waterhemp (Amaranthus rudis) resistant to triazine and ALS herbicides. Weed Sci. 46:514520.Google Scholar
Franey, R. J. and Hart, S. E. 1998. Absorption, translocation, and metabolism of cloransulam-methyl in three weed species. Weed Sci. Soc. Am. Abstr. 38:48.Google Scholar
Frear, D. S., Swanson, H. R., and Tanaka, F. S. 1993. Metabolism of flumetsulam (DE-498) in wheat, corn, and barley. Pestic. Biochem. Physiol. 45:178192.Google Scholar
Gerwick, B. C., Subramanian, M. V., and Loney-Gallant, V. I. 1990. Mechanism of action of the 1,2,4-trizolo[1,5-a]pyrimidines. Pestic. Sci. 29:357364.Google Scholar
Heap, I. 2001. International survey of herbicide resistant weeds. Online, www.weedscience.com.Google Scholar
Hinz, J. R. and Owen, M.D.K. 1997. Acetolactate synthase resistance in a common waterhemp (Amaranthus rudis) population. Weed Technol. 11:1318.Google Scholar
Hodges, C. C., de Boer, G. J., and Avalos, J. 1990. Uptake and metabolism as mechanisms of selective herbicidal activity of 1,2,4-triazolo[1,5-a]pyrimidines. Pestic. Sci. 29:365378.CrossRefGoogle Scholar
Horak, M. J. and Peterson, D. E. 1995. Biotypes of Palmer amaranth (Amaranthus palmeri) and common waterhemp (Amaranthus rudis) are resistant to imazethapyr and thifensulfuron. Weed Technol. 9:192195.Google Scholar
Jensen, K.I.N. 1982. The roles of uptake, translocation, and metabolism in the differential intraspecific responses to herbicides. Pages 133162 In LeBaron, H. M. and Gressel, J., eds. Herbicide Resistance in Plants. New York: J. Wiley.Google Scholar
Lovell, S. T., Wax, L. M., Horak, M. J., and Peterson, D. E. 1996. Imidazolinone and sulfonylurea resistance in a biotype of common waterhemp (Amaranthus rudis). Weed Sci. 44:789794.Google Scholar
Manley, B. S., Hatzios, K. K., and Wilson, H. P. 1999a. Absorption, translocation, and metabolism of chlorimuron and nicosulfuron in imidazolinone-resistant and susceptible smooth pigweed (Amaranthus hybridus). Weed Technol. 13:759764.Google Scholar
Manley, B. S., Singh, B. K., Shaner, D. L., and Wilson, H. P. 1999b. Imidazolinone resistance in smooth pigweed (Amaranthus hybridus) is due to an altered acetolactate synthase. Weed Technol. 13:697705.Google Scholar
Manley, B. S., Wilson, H. P., and Hines, T. E. 1996. Smooth pigweed (Amaranthus hybridus) and livid amaranth (A. lividus) response to several imidazolinone and sulfonylurea herbicides. Weed Technol. 10:835841.Google Scholar
Manley, B. S., Wilson, H. P., and Hines, T. E. 1998. Characterization of imidazolinone-resistant smooth pigweed (Amaranthus hybridus). Weed Technol. 12:575584.Google Scholar
Murdock, E. C., Keeton, A., Smith, J. D., Fowler, J. T. Jr., and Toler, J. E. 1998. Sicklepod, pitted morningglory, and Palmer amaranth control in soybean with cloransulam-methyl. Proc. South. Weed Sci. Soc. 51:64.Google Scholar
Nelson, K. A. and Renner, K. A. 1998. Postemergence weed control with CGA-277476 and cloransulam-methyl in soybean (Glycine max). Weed Technol. 12:293299.Google Scholar
Oliver, L. R., Gander, J. R., Starkey, R. J., and Barrentine, J. L. 1997. Weed control programs with Firstrate (cloransulam). Proc. South. Weed Sci. Soc. 50:1617.Google Scholar
Poston, D. H., Wilson, H. P., and Hines, T. E. 2000. Imidazolinone resistance in several Amaranthus hybridus populations. Weed Sci. 48:508513.Google Scholar
Santel, H. J., Bowden, B. A., Sorensen, V. M., Mueller, K. H., and Reynolds, J. 1999. Flucarbozone-sodium: a new herbicide for grass control in wheat. Abstr. Weed Sci. Soc. Am. 39:7.Google Scholar
Shaner, D. L., Anderson, P. C., and Stidham, M. A. 1984. Imidazolinones: potent inhibitors of acetohydroxyacid synthase. Plant Physiol. 76:545546.Google Scholar
Simpson, D. M. 1998. Understanding and preventing development of ALS-resistant weed populations. Down Earth 53:2635.Google Scholar
Sprague, C. L., Stoller, E. W., Wax, L. M., and Horak, M. J. 1997. Palmer amaranth (Amaranthus palmeri) and common waterhemp (Amaranthus rudis) resistance to selected ALS-inhibiting herbicides. Weed Sci. 45:192197.Google Scholar
Stidham, M. A. 1991. Herbicides that inhibit acetohydroxyacid synthase. Weed Sci. 39:428434.Google Scholar
Subramanian, M. V., Hung, H., Dias, J. M., Miner, V. W., Butler, J. H., and Jachetta, J. J. 1990. Properties of mutant acetolactate synthase resistant to triazolopyrimidine sulfonanilides. Plant Physiol. 94:239244.Google Scholar