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Photosynthesis and Transpiration Response of Redroot Pigweed (Amaranthus retroflexus)

Published online by Cambridge University Press:  12 June 2017

David C. Nielsen
Affiliation:
U.S. Dep. Agric., Akron, CO 80720
Randy L. Anderson
Affiliation:
U.S. Dep. Agric., Akron, CO 80720

Abstract

Redroot pigweed is a major weed worldwide. Increasing emphasis on modeling physiological processes of weeds for use in weed control decision support systems requires a knowledge of the response of weeds to resource levels and environmental conditions. The purpose of this study was to determine functional relationships for carbon exchange rate (CER) and transpiration based on photosynthetic photon flux density (PPFD) and temperature from measurements made on field-grown redroot pigweed. Measurements were made using a portable photosynthesis system on four dates. An equation that had the form of a power function on PPFD and a quadratic polynomial on temperature was fit to the data. The equation fit the measured CER data better than the measured transpiration data. The equations should be useful in modeling the physiological processes of pigweed within crop canopies.

Type
Research
Copyright
Copyright © 1994 by the Weed Science Society of America 

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References

Literature Cited

1. Ahrens, W. H. and Stoller, E. W. 1983. Competition, growth rate, and CO2 fixation in triazine-susceptible and -resistant smooth pigweed (Amaranthus hybridus). Weed Sci. 31:438444.Google Scholar
2. Chu, Chang-chi, Ludford, P. M., Ozbun, J. L., and Sweet, R. D. 1978. Effects of temperature and competition on the establishment and growth of redroot pigweed and common lambsquarters. Crop Sci. 18:308310.Google Scholar
3. Coleman, J. S. and Bazzaz, F. A. 1992. Effects of CO2 and temperature on growth and resource use of co-occurring C3 and C4 annuals. Ecology 73:12441259.Google Scholar
4. El-Sharkawy, M. A., Cock, J. H., and Hernandez, A. D. P. 1985. Stomatal response to air humidity and its relation to stomatal density in a wide range of warm climate species. Photosynth. Res. 7:137149.Google Scholar
5. Garbutt, K., Williams, W. E., and Bazzaz, F. A. 1990. Analysis of the differential response of five annuals to elevated CO2 during growth. Ecology 71:11851194.Google Scholar
6. Holt, J. S. 1991. Applications of physiological ecology to weed science. Weed Sci. 39:521528.CrossRefGoogle Scholar
7. Kropff, M. J. and Lotz, L. A. P. 1992. Optimization of weed management systems: The role of ecological models of interplant competition. Weed Technol. 6:462470.Google Scholar
8. Kuo, J., Fox, E., Mitchell, D., and Tuerke, T. 1992. Transforms and curve fitting. Jandel Scientific, San Rafael, CA. p. 616.Google Scholar
9. Patterson, D. T. 1976. C4 photosynthesis in smooth pigweed. Weed Sci. 24:127130.CrossRefGoogle Scholar
10. Singh, M., Ogren, W. L., and Widholm, J. M. 1974. Photosynthetic characteristics of several C3 and C4 plant species grown under different light intensities. Crop Sci. 14:563566.Google Scholar
11. Weaver, S. E. and McWilliams, E. L. 1980. The biology of Canadian weeds. 44. Amaranthus retroflexus L., A. powellii S. Wats. and A. hybridus L. Can. J. Plant Sci. 60:12151234.Google Scholar
12. West, L. D., Muzik, T. J., and Witters, R. E. 1976. Differential gas exchange responses to two biotypes of redroot pigweed to atrazine. Weed Sci. 24:6872.Google Scholar
13. Wilkerson, G. G., Jones, J. W., Coble, H. D., and Gunsolus, J. L. 1990. SOYWEED: A simulation model of soybean and common cocklebur growth and competition. Agron. J. 82:10031010.Google Scholar