Compound-specific isotope analysis (CSIA) is a powerful approach to evaluate the transformation of organic pollutants in the environment. However, the application of CSIA to micropollutants, such as pesticides, remains limited because appropriate extraction methods are currently lacking. Such methods should address a wide range of pesticides and environmental matrices, while recovering sufficient mass for reliable CSIA without inducing stable isotope fractionation. Here, we present simple extraction methods for carbon and nitrogen CSIA for different environmental matrices and six commonly used herbicides, i.e., atrazine, terbutryn, acetochlor, alachlor, butachlor, and S-metolachlor, and three fungicides, i.e., dimethomorph, tebuconazole, and metalaxyl. We examined the potential of several extraction methods for four types of soils or sediments, three types of environmental waters and aerial and root plant samples for multielement (ME)-CSIA.•Pesticide extraction recoveries varied depending on the physical characteristics of the pesticides and matrix properties for environmental water (77 to 87%), soil and sediment (35 to 82%), and plant (40 to 59%) extraction.•The tested extraction methods did not significantly affect the carbon and nitrogen stable isotope signatures of pesticides (Δ(13C) <0.9‰ for Δ(15N) <1.0‰).
Keywords: CSIA; Pesticide extraction; degradation; stable isotopes; transformation products.
© 2022 The Author(s). Published by Elsevier B.V.