4.7 Article

Investigation of the spatial variability of poly- and perfluoroalkyl substance trophic magnification in selected riverine ecosystems

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 686, Issue -, Pages 393-401

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2019.05.461

Keywords

PFASs; River; Trophic magnification factors; Biotransfonnation; Spatial variability

Funding

  1. Onema [ANR-10-LABX-45]
  2. CPER A2E (Aquitaine region)
  3. CPER A2E (FEDER (Europe is moving in Aquitaine with the European Regional Development Fund (FEDER))

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The occurrence at different trophic levels of 17 poly- and perfluoroalkyl substances (PFASs), including perfluoroalkyl adds (PFAAs) and some of their precursors (e.g., perfluoroalkane sulfonamides, 6:2 fluorotelomer sulfonate (6:2 VISA)), was investigated in riverine freshwater food webs in Southeastern France. Two fish spedes (Barbus barbus and Squalius cephalus) and various invertebrate taxa were collected in five rivers to assess the spatial variability of trophic magnification factors (TMFs). Particular attention was devoted to sample and data processing to minimize potential biases assodated with the TMF determination. Fish were significantly more contaminated than invertebrates (Sigma PFAS - 7-1811 vs. 0.9-213 ng g(-1) wet weight (ww)). Those from the Rhone River presented significantly higher levels due to high concentrations of perfluoroundecanoic add (406 ng g(-1) ww) and perfluorotridecanoic acid (566 ng g(-1) ww) ascribed to an industrial point source. Perfluorooctane sulfonate (PFOS) was dominant at the other sites (concentration range= 3.6-134 ng g(-1) ww). Two linear regression models were compared (i.e., Kendall regression vs. Generalized Linear Mixed-Effect Model, GLMM). Results showed that TMFs calculated using the non-weighted Kendall regression were higher than those obtained using the GLMM approach. GLMM-based TMFs were consistently >1 for C-9-C-14 perfluorocarboxylic acids (PFCAs). PFOS and perfluorodecane sulfonate (PFDS), indicating their apparent biomagnification in the investigated food webs. Comparatively, 6:2 FTSA and N-ethylperfluorooctane sulfonamidoacetic acid (N-EtFOSAA) were less often detected and were not significantly biomagnified, probably because of metabolization. TMF estimates were generally consistent across sites although some PFASs (in particular C-9, C-10 and C-13 PFCAs) displayed higher variability, due to a unique extreme value that may have resulted from the contribution of unattributed precursor biotransformation. (C) 2019 Elsevier B.V. All rights reserved.

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