Abstract
QuEChERS and solid phase extraction (SPE) methods were applied for determining four herbicides (metazachlor, oxyfluorfen, quizalofop-p-ethyl, quinmerac) and one insecticide (α(±)-cypermethrin) in runoff water, soil, sunflower and oilseed rape plant matrices. Determination was performed using gas chromatography mass spectrometry (GC-MS), whereas high-pressure liquid chromatography mass spectrometry (HPLC-MS) was used for quinmerac. In all substrates linearity was evaluated using matrix-matched calibration samples at five concentration levels (50–1000 ng L−1 for water, 5–500 μg kg−1 for soil and 2.5–500 μg kg−1 for sunflower or oilseed rape plant). Correlation coefficient was higher than 0.992 for all pesticides in all substrates. Acceptable mean recovery values were obtained for all pesticides in water (65.4–108.8%), soil (70.0–110.0%) and plant (66.1–118.6%), with intra- and inter-day RSD% below 20%. LODs were in the range of 0.250–26.6 ng L−1 for water, 0.10–1.8 μg kg−1 for soil and 0.15–2.0 μg kg−1 for plants. The methods can be efficiently applied for field dissipation studies of the pesticides in energy crop cultivations.
Acknowledgements
This research has been co-financed by the European Union (European Social Fund – ESF) and Greek national funds through the Operational Program ‘Education and Lifelong Learning’ of the National Strategic Reference Framework (NSRF) – Research Funding Program: ARCHIMEDES III. Investing in knowledge society through the European Social Fund.
This work was first presented at the 7th European Conference on Pesticides and Related Organic Micropollutants in the Environment and 13th Symposium on Chemistry and Fate of Modern Pesticides, 7–10 October 2012, Porto, Portugal.