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Mechanism of Clomazone Selectivity in Corn (Zea mays), Soybean (Glycine max), Smooth Pigweed (Amaranthus hybridus), and Velvetleaf (Abutilon theophrasti)

Published online by Cambridge University Press:  12 June 2017

Rex A. Liebl
Affiliation:
Dep. Agron., Univ. Illinois, 1102 S. Goodwin Ave., Urbana, IL 61801
Michael A. Norman
Affiliation:
Dep. Agron., Univ. Illinois, 1102 S. Goodwin Ave., Urbana, IL 61801

Abstract

Based on chlorophyll content, hydroponically cultured soybean seedlings were 254, 66, and 13 times more tolerant to clomazone than velvetleaf, corn, and smooth pigweed, respectively. Clomazone, at concentrations that inhibited chlorophyll, did not affect fresh weight accumulations of any species except velvetleaf. However, in velvetleaf, fresh weight accumulation was only half as sensitive to clomazone as the leaf chlorophyll content. Uptake of 14C-clomazone from nutrient solution by 72 h after treatment (HAT) (pigweed > velvetleaf > soybean > corn) indicates that differential absorption cannot account for selectivity. Shoot:root ratios of 14C recovered from soybean, corn, velvetleaf, and pigweed by 72 HAT were 0.39, 0.84, 1.67, and 2.37, respectively. The limited acropetal clomazone translocation in soybean seedlings may account to a small degree for soybean tolerance to clomazone. Conversion of clomazone to more polar metabolites was rapid in all four species. There were no significant differences among species in the percentage of 14C activity recovered as clomazone from root tissue by 72 HAT. Of the 14C activity recovered from shoots of soybean, corn, pigweed, and velvetleaf seedlings by 72 HAT, 46, 59, 35, and 54%, respectively, was clomazone. Differences in clomazone uptake, distribution, and metabolism among the four species were either insignificant or poorly correlated to selectivity, and therefore cannot account for the tremendous differences in clomazone sensitivity among these species. These observations indicate, indirectly, that differences at the site of action may account for selectivity.

Type
Physiology, Chemistry, and Biochemistry
Copyright
Copyright © 1991 by the Weed Science Society of America 

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References

Literature Cited

1. Cantwell, J. R., Liebl, R. A., and Wax, L. M. 1987. Soybean weed control with soil applied herbicides. N. Cent. Weed Control Conf. Res. Rep. 44:280281.Google Scholar
2. Curran, W. S. and Paul, L. E. 1987. Response of four corn hybrids to reduced rates of clomazone, imazaquin, imazethapyr and chlorimuron. N. Cent. Weed Control Conf. Res. Rep. 44:177.Google Scholar
3. Duke, S. O., Kenyon, W. H., and Paul, R. N. 1985. FMC 57020 effects on chloroplast development in pitted morningglory (Ipomoea lacunosa) cotyledons. Weed Sci. 33:786794.CrossRefGoogle Scholar
4. Duke, S. O. and Kenyon, W. H. 1986. Effects of dimethazone (FMC 57020) on chloroplast development, II. Pigment synthesis and photosynthetic function in cowpea (Vigna unguiculata L.) primary leaves. Pestic. Biochem. Physiol. 25:1118.CrossRefGoogle Scholar
5. Hoagland, D. R. and Arnon, D. I. 1950. The water culture method of growing plants without soil. Calif. Agric. Exp. Stn. Circ. 347. 32 pp.Google Scholar
6. Holden, M. 1976. Chlorophylls. Pages 137 in Goodwin, T. W., ed. Chemistry and Biochemistry of Pigments. Vol. 2. Academic Press, New York.Google Scholar
7. Kapusta, G. and Anderson, J. S. 1987. Soybean weed control with preplant incorporated clomazone plus imazaquin or imazethapyr. N. Cent. Weed Control Conf. Res. Rep. 44:282283.Google Scholar
8. Norman, M. A., Liebl, R. A., and Widholm, J. M. 1990. Uptake and metabolism of clomazone in tolerant soybean and susceptible cotton photomixotrophic cell suspension cultures. Plant Physiol. 92:777784.Google Scholar
9. Norman, M. A., Liebl, R. A., and Widholm, J. M. 1990. Site of clomazone action in tolerant-soybean and susceptible-cotton photomixotrophic cell suspension cultures. Plant Physiol. 94:704709.Google Scholar
10. Sandmann, G. and Boger, P. 1987. Interconversion of prenyl pyrophosphates and subsequent reactions in the presence of FMC-57020. Z. Naturforsch. 42c:803807.Google Scholar
11. Vencill, W. K., Hatzios, K. K., and Wilson, H. P. 1990. Absorption, translocation and metabolism of 14C-clomazone in soybean (Glycine max) and three Amaranthus weed species. J. Plant Growth Regul. 9:127132.Google Scholar
12. Westberg, D. E., Oliver, L. E., and Frans, R. E. 1989. Weed control with clomazone and with other herbicides. Weed Technol. 3:678685.CrossRefGoogle Scholar
13. Weston, L. A. and Barrett, M. 1989. Tolerance of tomato (Lycopersicon esculentum) and bell pepper (Capsicum annum) to clomazone. Weed Sci. 37:285289.Google Scholar