Photodegradation of Rotenone in Soils under Environmental Conditions

Ivana Cavoski,* Pierluigi Caboni, Giorgia Sarais, Paolo Cabras, and Teodoro Miano
Dipartimento di Biologia e Chimica Agroforestale ed Ambientale, Universit degli Studi di Bari, Via Amendola 165/A, 70126 Bari, Italia, and Dipartimento di Tossicologia, Universit di Cagliari, Via Ospedale 72, 09124 Cagliari, Italia
J. Agric. Food Chem., 2007, 55 (17), pp 7069–7074
DOI: 10.1021/jf0708239
Publication Date (Web): July 21, 2007
Copyright © 2007 American Chemical Society
*

 To whom correspondence should be addressed. E-mail:  ivana.cavoski@agr.uniba.it.

,

 Università degli Studi di Bari.

,

 Università di Cagliari.

Abstract

Abstract Image

An environmental fate study was performed to analyze the effects of soil components on the photochemical behavior of rotenone. Photodegradation experiments were carried out on three types of soil collected in southern Italy, Valenzano (VAL), Turi (TUR), and Conversano (CON), from April to June 2006. Soil thin-layer plates (1 mm thick) were spiked with 1.5 mg/kg of rotenone and exposed under natural conditions of sunlight and temperature. The plates were removed from the sunlight at predetermined intervals of continuous irradiation. Other soil samples, control and sterilized, were kept in the dark to evaluate possible effects of chemical and microbiological degradation during the irradiation experiment. The time for 50% loss of the initially applied rotenone varied from 5 to 7 h, following the order TUR < CON < VAL. In environmental studies, changes in temperature and/or moisture affected the degradation rate and caused deviations from first-order kinetics. The photolysis reaction fit the two compartment or the multiple compartment model pathways better. A fast initial decrease during the first 5 h of rotenone irradiation was followed by a much slower decline, which clearly indicates the rather complex chemical process of rotenone photodegradation on soil surfaces. Also, the degradation was shown to be directly related to the soil concentration of clay and organic matter. Rotenolone (12aβ-hydroxyrotenone) was detected by HPLC/DAD/MS analysis as the only photodegradation byproduct of rotenone in soil thin layers. Results provide additional insights on the rates and the mechanisms of rotenone degradation, aiming to describe more clearly the degradation performance of chemical residues in the environment.

Keywords: Rotenone; environmental fate; half-life; soil photolysis; LC/MS

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History

  • Published In Issue August 22, 2007
  • Received for review March 20, 2007. Revised manuscript received June 13, 2007. Accepted June 15, 2007.

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