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Physiological basis for CGA-248757 and flumiclorac selectivity in five plant species

Published online by Cambridge University Press:  20 January 2017

Jason C. Fausey ,
Donald Penner  and
Karen A. Renner
Jason C. Fausey
Affiliation:
Department of Crop and Soil Sciences, Michigan State University, East Lansing, MI 48824-1325
Donald Penner
Affiliation:
Department of Crop and Soil Sciences, Michigan State University, East Lansing, MI 48824-1325
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Abstract

Greenhouse and laboratory studies were conducted to determine the physiological basis for CGA-248757 and flumiclorac selectivity in five plant species. CGA-248757 and flumiclorac selectively control weeds postemergence (POST) by inhibiting protoporphyrinogen oxidase (Protox). Injury symptoms from CGA-248757 and flumiclorac include rapid desiccation and necrosis similar to injury from diphenyl ether and bipyridinium herbicides. Species sensitivity to CGA-248757 and flumiclorac was evaluated by comparing the dry weight reduction from POST applications. Abutilon theophrasti was sensitive to both herbicides, Amaranthus retroflexus was more sensitive to flumiclorac than CGA-248757, Brassica kaber was sensitive to CGA-248757 but tolerant of flumiclorac, and Zea mays and Glycine max were tolerant of both herbicides. Studies evaluated CGA-248757 and flumiclorac retention, absorption, translocation, and metabolism. Enhanced herbicide metabolism contributed to the tolerance of A. retroflexus to CGA-248757 and B. kaber to flumiclorac. Decreased herbicide retention, absorption, and translocation coupled with increased metabolism contributed to Z. mays tolerance of CGA-248757 and flumiclorac. Decreased herbicide retention and increased herbicide metabolism provided G. max tolerance of both herbicides.

Keywords

CGA-248757, [[2-chloro-4-fluoro-5-[(tetrahydro-3-oxo-1H, 3H-[1,3,4]thiadiazolo[3,4-a]pyridazin-1-ylidene)amino]phenyl]thio]acetateflumicloracAbutilon theophrasti Medicus ABUTH, velvetleafAmaranthus retroflexus L. AMARE, redroot pigweedBrassica kaber (D.C.) L.C. Wheeler SINAR, wild mustardGlycine max (L.) Merr. ‘Conrad,’ soybeanZea mays L. ‘Pioneer 3751,’ cornAbsorptionmetabolismprotoporphyrinretentiontranslocationGlycine maxZea maysABUTHAMARESINAR
Type
Research Article
Information
Weed Science , Volume 48 , Issue 4 , August 2000 , pp. 405 - 411
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Anonymous. 1995. Fluthiacet herbicide technical information bulletin. Greensboro, NC: CIBA-GEIGY Corp., Agricultural Division.Google Scholar
Boldt, P. F. and Putnam, A. R. 1980. Selectivity mechanisms for foliar applications of diclofop-methyl. I. Retention, absorption, translocation, and volatility. Weed Sci. 28:474–477.Google Scholar
Doran, D. L. and Andersen, R. N. 1976. Effectiveness of bentazon applied at various times of day. Weed Sci. 24:567–570.Google Scholar
Duke, S. O., Becerril, J. M., Sherman, T. D., Lydon, J., and Matsumoto, H. 1990. The role of protoporphyrin IX in the mechanism of action of diphenyl ether herbicides. Pestic. Sci. 30:367–378.Google Scholar
Duke, S. O., Lydon, J., Becerril, J. M., Sherman, T. D., Lehnen, L. P. Jr., and Matsumoto, H. 1991. Protoporphyrinogen oxidase-inhibiting herbicides. Weed Sci. 39:465–473.Google Scholar
Duke, S. O., Vaughn, K. C., and Meeusen, R. L. 1984. Mitochondrial involvement in the mode of action of acifluorfen. Pestic. Biochem. Physiol. 21:368–373.Google Scholar
Gillespie, G. R. 1994. Basis for the differential response of quackgrass (Elytrigia repens) biotypes to primisulfuron. Weed Sci. 49:8–12.Google Scholar
Gullner, G., Kiraly, L., and Komives, T. 1991. Nitrodiphenyl ether and phenylimide resistance of a tobacco biotype is due to enhanced inducibility of its antioxidant systems. Pages 1111–1118 in Proceedings of the Brighton Crop Protection Conference-Weeds.Google Scholar
Harr, J., Guggenheim, R., Schulke, G., and Falk, R. H. 1991. The leaf surface of major weeds. Basel, Switzerland: Sandoz Agro, Ltd.Google Scholar
Harrison, S. K. and Wax, L. M. 1986. Adjuvant effects on absorption, translocation, and metabolism of haloxyfop-methyl in corn (Zea mays). Weed Sci. 34:185–195.Google Scholar
Hatzios, K. K. and Penner, D. 1985. Interactions of herbicides with other agrochemicals in higher plants. Rev. Weed Sci. 1:1–63.Google Scholar
Higgins, J. M., Whitwell, T., Corbin, F. T., Carter, G. E. Jr., and Hill, H. S. Jr. 1988. Absorption, translocation, and metabolism of acifluorfen and lactofen in pitted morningglory (Ipomoea lacunosa) and ivyleaf morningglory (Ipomoea hederacea). Weed Sci. 36:141–145.Google Scholar
Jacobs, J. M., Jacobs, N. J., Sherman, T. D., and Duke, S. O. 1991. Effect of diphenyl ether herbicides on oxidation of protoporphyrinogen to protoporphyrin in organellar and plasma membrane enriched fractions of barley. Plant Physiol. 97:197–203.Google Scholar
Jacobs, J. M., Jacobs, N. J., Borotz, S. F., and Guerinot, M. L. 1990. Effects of photobleaching herbicide, acifluorfen-methyl, on protoporphyrinogen oxidation in barley organelles, soybean root mitochondria, soybean root nodules, and bacteria. Arch. Biochem. Biophys. 280:369–375.Google Scholar
Kamoshita, K., Nagano, E., Hashimoto, S., Sato, R., Yoshida, R., and Oshio, H. 1993. V-23031—A new herbicide for postemergence weed control in soybeans and field corn. Abstr. Weed Sci. Soc. Am. 53:3.Google Scholar
Kells, J. J., Meggitt, W. F., and Penner, D. 1984. Absorption, translocation, and activity of fluazifop-butyl as influenced by plant growth stage and environment. Weed Sci. 32:143–149.Google Scholar
King, C. A. and Oliver, L. R. 1992. Application rate and timing of acifluorfen, bentazon, chlorimuron, and imazaquin. Weed Technol. 6:526–534.Google Scholar
Kurtz, A. R. and Pawlak, J. A. 1993. V-23031—A new postemergence herbicide for use in field corn. Abstr. Weed Sci. Soc. Am. 53:9.Google Scholar
Lydon, J. and Duke, S. O. 1988. Porphyrin synthesis is required for photobleaching activity of the p-nitrosubstituted diphenyl ether herbicides. Pestic. Biochem. Physiol. 31:74–83.Google Scholar
Mito, N., Sato, R., Miyakado, M., Oshio, H., and Tanaka, S. 1991. In vitro mode of action of N-Phenylimide photobleaching herbicides. Pestic. Biochem. Physiol. 40:128–135.Google Scholar
Porpiglia, P. J., Hill, E. R., and Tally, A. 1994. CGA-248757 for postemergence broadleaf weed control in corn (Zea mays L.) and soybeans (Glycine max (L.) Merr.). Abstr. Weed Sci. Soc. Am. 34:2.Google Scholar
Ritter, R. L. and Coble, H. D. 1981. Penetration, translocation, and metabolism of acifluorfen in soybean (Glycine max), common ragweed (Ambrosia artemisiifolia), and common cocklebur (Xanthium pensylvanicum). Weed Sci. 29:474–480.Google Scholar
Roggenbuck, F. C., Rowe, L., Penner, D., Petroff, L., and Burrow, R. 1990. Increasing postemergence herbicide efficacy and rainfastness with silicone adjuvants. Weed Technol. 4:576–580.Google Scholar
Sandmann, G. and Böger, P. 1990. Peroxidizing herbicides: Some aspects on tolerance. Washington D.C.: American Chemical Society Symposium Series No. 421, pp. 407–418.Google Scholar
Sato, R., Oshio, H., Koike, H., Inoue, Y., Yoshida, S., and Takahashi, N. 1991. Specific binding of protoporphyrin IX to membrane-bound 63 kilodalton polypeptide in cucumber cotyledons treated with diphenyl ether-type herbicides. Plant Physiol. 96:432–437.Google Scholar
Scalla, R. and Matringe, M. 1994. Inhibitors of protoporphyrinogen oxidase as herbicides: Diphenyl ethers and related photobleaching molecules. Rev. Weed Sci. 6:103–132.Google Scholar
Sherman, T. D., Becerril, J. M., Matsumoto, H., Duke, M. V., Jacobs, J. M., Jacobs, N. J., and Duke, S. O. 1991. Physiological basis for differential sensitivities of plant species to protoporphyrinogen oxidase-inhibiting herbicides. Plant Physiol. 97:280–287.Google Scholar
Sprague, C. L., Penner, D., and Kells, J. J. 1999. Weed control and Zea mays tolerance as affected by timing of RP-201772 application. Weed Sci. 47:375–382.Google Scholar
Starke, R. J., Renner, K. A., Penner, D., and Roggenbuck, F. C. 1996. Influence of adjuvants and desmedipham plus phenmedipham on velvetleaf (Abutilon theophrasti) and sugarbeet response to triflusulfuron. Wed Sci. 44:489–495.Google Scholar
Westberg, D. E. and Coble, H. D. 1992. Effect of acifluorfen on the absorption, translocation, and metabolism of chlorimuron in certain weeds. Weed Technol. 6:4–12.Google Scholar
Wichert, R. A. and Talbert, R. E. 1992. Soybean [Glycine max (L.)] response to lactofen. Weed Sci. 41:23–27.Google Scholar
Wright, T. R., Fuerst, E. P., Ogg, A. G. Jr., Nandihalli, U. B., and Lee, H. J. 1995. Herbicidal activity of UCC-C4243 and acifluorfen is due to inhibition of protoporphyrinogen oxidase. Weed Sci. 43:47–54.Google Scholar