Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractDetermination of short-chain carboxylic acids and non-targeted analysis of water samples treated by wet air oxidation using gas chromatography-mass spectrometry    Next AbstractEx-situ bioremediation of chlorobenzenes in soil »

Environ Pollut


Title:A biological loss of endosulfan and related chlorinated organic compounds from aqueous systems in the presence and absence of oxygen
Author(s):Guerin TF;
Address:"Shell Engineering Ltd, NSW State Office, PO Box 26, Granville 2142 NSW, Australia. turlough.guerin@shell.com.au"
Journal Title:Environ Pollut
Year:2001
Volume:115
Issue:2
Page Number:219 - 230
DOI: 10.1016/s0269-7491(01)00112-9
ISSN/ISBN:0269-7491 (Print) 0269-7491 (Linking)
Abstract:"Endosulfan is a cyclodiene organochlorine currently widely used as an insecticide throughout the world. This study reports that the endosulfan isomers can be readily dissipated from aqueous systems at neutral pH in the absence of biological material or chemical catalysts, in the presence or absence of oxygen. The study showed that aldrin, dieldrin, and endosulfan exhibit bi-phasic loss from water in unsealed and butyl rubber sealed vessels. Half-lives are substantially increased for endosulfan I when oxygen is removed from the incubation vessel. The study conditions, where PTFE was used, were such that loss due to volatilization and alkaline chemical hydrolysis was eliminated. Half-lives determined from these data indicate that the parent isomers are much less persistent than the related cyclodienes, aldrin and dieldrin, confirming the findings of previous studies. The major oxidation product of endosulfans I and II, endosulfan sulfate, is less volatile and can persist longer than either of the parent isomers. Endosulfan sulfate was not formed in any of the treatments suggesting that it would not be formed in aerated waters in the absence of microbial activity or strong chemical oxidants. Since endosulfan sulfate is formed in many environments through biological oxidation, and is only slowly degraded (both chemically in sterile media and biologically), it represents a predominant residue of technical grade endosulfan, which finds its way into aerobic and anaerobic aquatic environments. The data obtained contributes to and confirms the existing body of half-life data on endosulfan I and II and its major oxidation product, endosulfan sulfate. The half-life data generated from the current study can be used in models for predicting the loss of chlorinated cyclodiene compounds from aqueous systems. The findings also highlight the importance of critically reviewing half-life data, to determine what the predominant processes are that are acting on the compounds under study"
Keywords:"Aerobiosis Aldrin/metabolism Anaerobiosis Biodegradation, Environmental Dieldrin/metabolism Endosulfan/*metabolism Half-Life Hydrogen-Ion Concentration Insecticides/*metabolism Isomerism Pesticide Residues/*metabolism Polytetrafluoroethylene/chemistry Ris;"
Notes:"MedlineGuerin, T F eng England 2001/11/15 Environ Pollut. 2001; 115(2):219-30. doi: 10.1016/s0269-7491(01)00112-9"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 19-12-2024