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Decay profile and metabolic pathways of quinalphos in water, soil and plants

Title
Decay profile and metabolic pathways of quinalphos in water, soil and plants
Author
RAHUL KUMAR
Keywords
Quinalphos; Degradation; Metabolic products; Chromatography; ORGANOPHOSPHORUS PESTICIDE; RESIDUES; CHROMATOGRAPHY; MONOCROTOPHOS; INSECTICIDES; DEGRADATION; HYDROLYSIS; TOXICITY; INDIA
Issue Date
2011-01
Publisher
PERGAMON-ELSEVIER SCIENCE LTD, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
Citation
Chemosphere,Vol.85 No.5 [2011],710-716
Abstract
The widespread occurrence of pesticide residues in different agricultural and food commodities has raised concern among the environmentalists and food chemists. In order to keep a proper track of these materials, studies on their decay profiles in the various segments of ecosystem under varying environmental conditions are needed. In view of this, the metabolites of quinalphos in water and soil under controlled conditions and in plants, namely tomato and radish in field conditions have been analysed and possible pathways suggested. In order to follow the decay of the pesticide, an HPLC procedure has been developed. Studies conducted in water at different temperatures, pH and organic content reveal that the persistence of the pesticide decreases with the increase in all the three variables. In the three different types of soils studied, the effect of pH is more or less apparent on a similar line. On an average a faster decay is observed in the case of plants than in water and soil. The decay profiles in all these cases follow first order kinetics. The metabolites were identified by GC-MS. The investigations reflect that degradation occurs through hydrolysis, S-oxidation, dealkylation and thiono-thiol rearrangement. The pathways seem to be complex and different metabolites were observed with the change in the matrix. Quinalphos oxon, O-ethyl-O-quinoxalin-2-yl phosphoric acid, 2-hydroxy quinoxaline and quinoxaline-2-thiol were observed in all the matrices. Results further indicate that the metabolites, 2-hydroxy quinoxaline and oxon, which are more toxic than parent compound, persist for a longer time. (C) 2011 Elsevier Ltd. All rights reserved.
URI
http://www.sciencedirect.com/science/article/pii/S0045653511006291?via%3Dihub
ISSN
0045-6535; 1879-1298
DOI
10.1016/j.chemosphere.2011.05.059
Appears in Collections:
COLLEGE OF ENGINEERING[S](공과대학) > EARTH RESOURCES AND ENVIRONMENTAL ENGINEERING(자원환경공학과) > Articles
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