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Herbicidal Effects on Crownvetch Rhizobia and Nodule Activity

Published online by Cambridge University Press:  12 June 2017

John Cardina
Affiliation:
Dep. Agron., The Pennsylvania State Univ., Univ. Park, PA 16802
Nathan L. Hartwig
Affiliation:
Dep. Agron., The Pennsylvania State Univ., Univ. Park, PA 16802
Felix L. Lukezic
Affiliation:
The Pennsylvania State Univ., Univ. Park, PA 16802

Abstract

Two strains of crownvetch (Coronilla varia L. # CZRVA) rhizobia were cultured in vitro with various rates of atrazine [6-chloro-N-ethyl-N′-(1-methylethyl)-1,3,5-triazine-2,4-diamine] and bifenox [methyl 5-(2,4-dichlorophenoxy)-2-nitrobenzoate]. Growth, measured turbidimetrically over 48 h, was similar for both strains. Atrazine and bifenox significantly reduced bacterial growth after 14 and 36 h, respectively, only at the highest concentrations tested (463 μM atrazine and 292 μM bifenox). Since growth of crownvetch rhizobia was apparently not affected by rates of atrazine or bifenox above reasonable soil solution concentrations, it is likely that herbicidal effects on nodulation were due to toxicity to the host plant rather than toxicity to these bacteria. In a growth chamber experiment, total nodule activity (TNA) and carbon dioxide exchange rate (CER) were measured simultaneously in an effort to distinguish direct atrazine effects on nodule function from indirect effects due to inhibition of photosynthesis and a resulting decrease in photosynthate supply to nodules. When 5 and 50 mg atrazine per kg soil were applied to intact plants, CER was severely reduced within 24 h, but similar reductions in TNA were not observed until 48 h after treatment. Total nodule activity was reduced similarly by atrazine and defoliation; the application of atrazine to defoliated plants did not inhibit TNA more than did defoliation alone. The data indicate that reductions in crownvetch nodule activity by atrazine are due to inhibition of photosynthesis or other processes rather than direct toxicity to N fixation.

Type
Physiology, Chemistry, and Biochemistry
Copyright
Copyright © 1986 by the Weed Science Society of America 

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References

Literature Cited

1. Anderson, J. R. 1978. Pesticide effects on non-target microorganisms. Pages 313533 in Hill, I. R. and Wright, S.J.L., eds. Pesticide Microbiology, Academic Press, New York.Google Scholar
2. Ashton, F. M., Gifford, E. M., and Bisalputra, T. 1963. Structural changes in Phaseolus vulgaris induced by atrazine. 1. Histological changes. Bot. Gaz. 124:329335.Google Scholar
3. Audus, L. J. 1964. Herbicide behavior in the soil. II. Interaction with soil microorganisms. Pages 163206 in Audus, L. J., ed. The Physiology and Biochemistry of Herbicides. Academic Press, New York.Google Scholar
4. Benthalenfalvay, G. J., Norris, R. F., and Phillips, D. A. 1979. Effect of bentazon, a Hill-reaction inhibitor, on symbiotic nitrogen fixing capacity and apparent photosynthesis. Plant Physiol. 63:213215.Google Scholar
5. Bergersen, F.J. 1980. Pages 40118 in Bergersen, F. J., ed. Methods for evaluating biological nitrogen fixation. John Wiley and Sons, New York.Google Scholar
6. Brock, J. L. 1972. Effects of the herbicide trifluralin and carbetamide on nodulation and growth of legume seedlings. Weed Res. 12:150154.Google Scholar
7. Cardina, J. and Hartwig, N. L. 1981. Influence of nitrogen and corn population on no-tillage corn yield with and without crownvetch. Proc. Northeast. Weed Sci. Soc. 35:2731.Google Scholar
8. Cardina, J. and Hartwig, N. L. 1985. Atrazine, bifenox, and shade effects on crownvetch nodulation. In review.Google Scholar
9. Carlyle, R. E. and Thorpe, J. D. 1947. Some effects of ammonium and sodium 2,4-D on legumes and the rhizobium bacteria. J. Am. Soc. Agron. 39:929936.Google Scholar
10. Fisher, D. J., Hays, A. L., and Jones, C. A. 1978. Effects of some surfactant fungicides on Rhizobium trifolii and its symbiotic relationship with white clover. Ann. Appl. Biol. 90:7384.CrossRefGoogle Scholar
11. Fletcher, W. W. 1956. Effect of hormone herbicides on the growth of Rhizobium trifolii . Nature Lond. 177:1244.Google Scholar
12. Greaves, M. P., Davies, H. A., Marsha, J.A.P., and Wingfield, G. I. 1976. Herbicides and soil microorganisms. Crit. Rev. Microbiol. 5:138.Google Scholar
13. Grossbard, E. 1970. Effect of herbicides on the symbiotic relationship between Rhizobium trifolii and white clover. Occ. Symp. Br. Grassld. Soc. 6:4759.Google Scholar
14. Grossbard, E. 1976. Effects on soil microflora. Pages 99147 in Audus, L. J., ed. Herbicides: Physiology, Biochemistry, Ecology. Academic Press, London.Google Scholar
15. Hartwig, N. L. 1974. Crownvetch makes a good sod for no-till corn. Crops Soils Mag. 27:1617.Google Scholar
16. Hoagland, D. R. and Arnon, D. I. 1950. The water culture method for growing plants without soil. Calif. Agric. Exp. Stn. Circ. 347.Google Scholar
17. Kapusta, G. and Rouwenhorst, D. L. 1973. Interaction of selected pesticides and Rhizobium japonicum in pure culture and under field conditions. Agron. J. 65:112115.Google Scholar
18. Moody, K., Kust, C. A., and Buchholtz, K. P. 1970. Uptake of herbicides by soybean roots in culture solution. Weed Sci. 18: 642647.Google Scholar
19. Raggio, M., Raggio, N., and Torrey, J. G. 1956. The interaction of nitrate and carbohydrates on rhizobial root nodule formation. Plant Physiol. 40:601604.Google Scholar