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Detection of the herbicide alachlor and its sulfonic acid metabolite in soil

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dc.contributor.advisor Bottomley, Peter J.
dc.creator Smith, Lesley A. (Lesley Anita), 1968-
dc.date.accessioned 2012-11-02T20:54:35Z
dc.date.available 2012-11-02T20:54:35Z
dc.date.copyright 1995-11-28
dc.date.issued 1995-11-28
dc.identifier.uri http://hdl.handle.net/1957/34795
dc.description Graduation date: 1996 en_US
dc.description.abstract The chloroacetanilide herbicide alachlor is the second most widely used herbicide in the US, where it is used on major crops such as corn and soybean. Although alachlor is mineralized slowly in soil, metabolites of alachlor have been found in soil indicating that alachlor is subject to chemical or biological transformation. A water-soluble, non-carcinogenic metabolite of alachlor, 2-[(2,6-diethlyphenyl) (methoxymethyl) amino]-2-oxoethane-sulfonic acid (ESA), has been detected in groundwater. Because ESA contains a sulfur atom it is likely that it was formed as a result of a glutathione-based transformation mechanism found in many organisms. The objectives of this study were to evaluate the use of an Enzyme-Linked ImmunoSorbent Assay (ELISA) to detect the herbicide alachlor and its ESA metabolite in soil, and to determine if alachlor and its ESA metabolite could be measured in a Willamette silt loam soil both before the planting, during the growth and after harvest of a sweet corn crop. Alachlor was analyzed by gas chromatography and ESA was analyzed by a commercial ELISA kit after separation of the two compounds by solid phase extraction (SPE). The SPE and ELISA systems were evaluated for efficiency of recovery and day-to-day variability. Although satisfactory recoveries were achieved with the SPE system, there was some amount of variability in quantifying ESA with the ELISA system. Measures taken to minimize variability included frequent calibration of the system and the inclusion of appropriate controls in each analysis. Alachlor levels were below the detection limit (<100 μg/kg soil) two months after application, whereas ESA was detected throughout the soil profile (0-100 cm) at 13.7-61.2 μg/kg between July and September. In December the level of ESA dropped substantially, and was below the detection limit in soil collected in April and June of the following year. A laboratory study provided evidence that the transformation of alachlor to ESA in Willamette soil was microbiologically mediated, but the question as to what extent plants, bacteria, or fungi carry out the transformation under field conditions remains unresolved. en_US
dc.language.iso en_US en_US
dc.subject.lcsh Alachlor -- Measurement en_US
dc.subject.lcsh Metabolites -- Measurement en_US
dc.title Detection of the herbicide alachlor and its sulfonic acid metabolite in soil en_US
dc.type Thesis/Dissertation en_US
dc.degree.name Master of Science (M.S.) in Soil Science en_US
dc.degree.level Master's en_US
dc.degree.discipline Agricultural Sciences en_US
dc.degree.grantor Oregon State University en_US
dc.description.digitization File scanned at 300 ppi (Monochrome, 8-bit Grayscale) using ScandAll PRO 1.8.1 on a Fi-6670 in PDF format. CVista PdfCompressor 4.0 was used for pdf compression and textual OCR. en_US
dc.description.peerreview no en_us


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