Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-11T07:58:29.500Z Has data issue: false hasContentIssue false

Weed Specificity of Alcohol Ethoxylate Surfactants Applied with Rimsulfuron

Published online by Cambridge University Press:  20 January 2017

Jerry M. Green*
Affiliation:
DuPont Crop Protection, Stine-Haskell Research Center Building 210, P.O. Box 30, Newark, DE 19714-0030

Abstract

The biological activity of rimsulfuron applied with 33 alcohol ethoxylate surfactants was determined on six economically important weed species. The surfactants had hydrophobes ranging from 6 to 24 carbons and hydrophiles ranging from 3 to 32 ethylene oxides (EOs), and the weeds had different leaf orientations, surface characteristics, and chemical compositions. In general, similar activity was observed among weed species with correlation coefficients ranging from 0.62 to 0.94. A few distinct species-specific differences were identified. For example, increasing surfactant size generally increased rimsulfuron activity on velvetleaf, but activity was reduced on giant foxtail with surfactants having the longest alkyl chain and the highest number of EO units. Increasing surfactant size increased common cocklebur control if the right balance between the hydrophobic and hydrophilic group was maintained. The optimum surfactant type with rimsulfuron across six species from both the empirical and the modeling results ranged from a hydrophobe with 17 carbons and a hydrophilic group with 20 to 30 EOs to 24 carbons and 13 EOs.

Type
Research
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

Green, J. M. 1999a. Optimizing alcohol ethoxylate surfactant activity at low doses. Weed Technol. 13: 737740.Google Scholar
Green, J. M. 1999b. Effect on nonylphenol ethoxylation on the biological activity of three herbicides with different water solubilities. Weed Technol. 13: 840842.Google Scholar
Green, J. M., Douchet, J. P., Reheis, A., Sanchis, P., Kreidi, M., and Coret, J. 1995. DPX-KG691—a new surfactant for sulfonylurea herbicides. Six-teenth International Columa Conference on Weed Control, December 6-8, 1995. Reims, France: National Association for Plant Protection. pp. 469475.Google Scholar
Harr, J., Guggenheim, R., Schulke, G., and Falk, R. H. 1991. The Leaf Surface of Major Weeds. Sandoz Agro, Ltd. Witerswil, Switzerland: Fricker Press. 131 p.Google Scholar
Hess, F. D. and Foy, C. L. 2000. Interaction of surfactants with plant cuticles. Weed Technol. 14: 807813.Google Scholar
Reddy, K. N., Locke, M. A., and Howard, K. D. 1995. Bentazon spray retention, activity, and foliar washoff in weed species. Weed Technol. 9: 773778.Google Scholar
Reddy, K. N. and Singh, M. 1992. Organosilicone adjuvant effects on glyphosate efficacy and rainfastness. Weed Technol. 6: 361365.Google Scholar
Stock, D. and Holloway, P. J. 1993. Possible mechanisms for surfactant induced foliar uptake of agrochemicals. Pestic. Sci. 38: 165177.Google Scholar
Government, U.S. 1987. Code of Federal Regulations, Title 40, Subchapter E, Part 180, Subpart D-180.1001. Washington: U.S. Government Printing Office.Google Scholar