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Persistence of Estrogenic Hormones in Agricultural Soils

II. 17{alpha}-Ethynylestradiol

Michael S. Colucci and Edward Topp*

Agriculture and Agri-Food Canada, Research Branch, 1391 Sandford Street, London, ON, Canada N5V 4T3



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Fig. 1. Structure of 17{alpha}-ethynylestradiol, a synthetic analogue of 17ß-estradiol modified by substitution of position 17 with an acetylene group.

 


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Fig. 2. Dissipation of 1 mg kg-1 17{alpha}-ethynylestradiol (open triangles) measured by high performance liquid chromatography (HPLC), and removal of yeast estrogenicity screen assay (YES)-detectable estrogenicity (closed triangle) 17{alpha}-ethynylestradiol in a loam soil adjusted to a moisture content of 15% and incubated at 30°C.

 


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Fig. 3. Dissipation of 1 mg kg-1 17{alpha}-ethynylestradiol by a loam soil adjusted to a moisture content of 13%, and incubated at 30°C. Nonsterile soil was incubated under an atmosphere of nitrogen gas (left panel) or air (center panel). Soil sterilized by autoclaving was incubated under air (right panel). Error bars indicate standard deviation.

 





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The SCI Journals Agronomy Journal Crop Science
Journal of Natural Resources
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Vadose Zone Journal
Soil Science Society of America Journal Journal of Plant Registrations The Plant Genome
Copyright © 2001 by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America.