4.7 Article

Photochemical interactions between pesticides and plant volatiles

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 807, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.scitotenv.2021.150716

关键词

Chlorothalonil; Imidacloprid; thyme's leaves; Photoreduction; Photooxidation; Photonitration

资金

  1. University Clemront-Auvergne/French Ministry of Higher Education and Research

向作者/读者索取更多资源

This study investigates the chemical reactions between pesticides and plant volatiles, both in solution and on plants, demonstrating the significance of these interactions. Reacting pesticides with plant metabolites can occur in various environmental compartments, highlighting the complexity of these scenarios.
Among the numerous studies devoted to the photodegradation of pesticides, very scarce are those investigating the effect of plant volatiles. Yet, pesticides can be in contact with plant volatiles after having been spread on crops or when they are transported in surface water, making interactions between the two kinds of chemicals possible. The objectives of the present study were to investigate the reactions occurring on plants. We selected thyme as a plant because it is used in green roofs and two pesticides: the fungicide chlorothalonil for its very oxidant excited state and the insecticide imidacloprid for its ability to release the radical NO2 under irradiation. Pesticides were irradiated with simulated solar light first in a solvent ensuring a high solubility of pesticides and plant volatiles, and then directly on thyme's leaves. Analyses were conducted by headspace gas chromatography- mass spectrometry (HS-GC-MS), GC-MS and liquid chromatography-high resolution mass spectrometry (LC-HRMS). In acetonitrile, chlorothalonil photosensitized the degradation of thymol, alpha-pinene, 3-carene and linalool with high quantum yields ranging from 0.35 to 0.04, and was photoreduced, while thymol underwent oxidation, chlorination and dimerization. On thyme's leave, chlorothalonil was photoreduced again and products arising from oxidation and dimerization of thymol were detected. Imidacloprid photooxidized and photonitrated thymol in acetonitrile, converting it into chemicals of particular concern. Some of these chemicals were also found when imidacloprid was irradiated dispersed on thyme's leaves. These results show that photochemical reactions be-tween pesticides and the plants secondary metabolites can take place in solution as on plants. These findings demonstrate the importance to increase our knowledge on these complex scenarios that concern all the environ-mental compartments. (C) 2021 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据