Occurrence and assessment of perfluorinated chemicals in wild fish from Northern Germany.

Chemosphere

Technical University of Berlin, Institute for Food Technology and Food Chemistry, Sekr. TIB 4/3-1, Gustav-Meyer-Allee 25, 13355 Berlin, Germany.

Published: February 2010

Residues of the perfluorinated chemicals perfluorooctanesulfonate (PFOS) and perfluorooctanoicacid (PFOA) were investigated in wild fish caught from different German waters including the North and the Baltic Sea, Lake Storkow in Brandenburg, several rivers in Lower Saxony, and rivers and lakes in the city of Berlin. The sample locations represent waters with no, low, medium and high portions of treated municipal sewage discharges. The investigated fish filet samples included 51 wild eels, 44 bream, 5 herring, 5 mackerel, 3 carp and 4 trout. PFOA was not found in any of the investigated samples above the limit of quantitation of 0.27 microgkg(-1) fresh weight (fw.), whereas PFOS was detected with concentrations up to 225 microgkg(-1)fw. PFOS was found in the filet samples caught from densely populated regions at levels between 8.2 and 225 microgkg(-1)fw. In samples from marine or remote locations, PFOS was not detected or only detected at levels up to 50.8 microgkg(-1)fw. To date, a tolerable daily intake (TDI) for PFOS and PFOA has or could not finally be fixed by any official national or international organization. A provisional TDI of 150 microgkg(-1) body weight per day has, however, been proposed by the European Food Safety Authority to be used for a provisional risk assessment. Thus, the detected residues of PFOS found in 33 out of 112 examined fish samples might be classified as potential risks for the health of consumers with elevated fish consumption.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.chemosphere.2009.12.015DOI Listing

Publication Analysis

Top Keywords

perfluorinated chemicals
8
wild fish
8
pfoa investigated
8
filet samples
8
pfos detected
8
225 microgkg-1fw
8
pfos
6
fish
5
samples
5
occurrence assessment
4

Similar Publications

The ground-state charge generation (GSCG) in photoactive layers determines whether the photogenerated carriers occupy the deep trap energy levels, which, in turn, affects the device performance of organic solar cells (OSCs). In this work, charge-quadrupole electrostatic interactions are modulated to achieve GSCG through a molecular strategy of introducing different numbers of F atom substitutions on the BTA3 side chain. The results show that 8F substitution (BTA3-8F) and 16F substitution (BTA3-16F) lead to different patterns of highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy level changes.

View Article and Find Full Text PDF

Photoredox-Enabled Direct and Three-Component Difluoroalkylative Modification of -Aryl Glycinates.

Org Lett

January 2025

Hubei Key Laboratory of Bioinorganic Chemistry & Materia Medica, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, 1037 Luoyu Road, Wuhan, Hubei 430074, China.

A Cu(I) photoredox-enabled reaction that selectively incorporates a difluoroalkyl group into -aryl glycine derivatives has been established. Using a bench-stable [PhPCFH]Br salt, the -CFH group could be installed either directly on the α-carbon of the glycine backbone or in a three-component fashion using an alkene as a bridge. A series of glycine derivatives have been evaluated, providing access to diverse unnatural amino esters and dipeptides with a -CHF unit.

View Article and Find Full Text PDF

Solid-State Photoswitching of Hydrazones Based on Excited-State Intramolecular Proton Transfer.

J Am Chem Soc

January 2025

Department of Organic Chemistry, Faculty of Natural Sciences, Comenius University, Ilkovičova 6, Bratislava SK-842 15, Slovakia.

The development of new photochromic systems is motivated by the possibility of controlling the properties and functions of materials with high spatial and temporal resolution in a reversible manner. While there are several classes of photoswitches operating in solution, the design of systems efficiently operating in the solid state remains highly challenging, mainly due to limitations related to confinement effects. Triaryl-hydrazones represent a relatively new subclass of bistable hydrazone photoswitches exhibiting efficient / photochromism in solution.

View Article and Find Full Text PDF

In this study, the results of a comprehensive assessment of the variability in the occurrence of ten perfluorinated compounds (PFAS) in fish tissues originating from 2014 to 2019 from six fisheries in the Baltic Sea are presented. A total of 360 fish samples of three species (perch, herring and flatfish) were analysed. For the determination of PFAS, both linear and branched stereoisomers, LC-ESI-MS/MS technique preceded by simultaneous SPE isolation was validated and applied.

View Article and Find Full Text PDF

Association Kinetics for Perfluorinated -Alkyl Radicals.

J Phys Chem A

January 2025

Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.

Radical-radical reaction channels are important in the pyrolysis and oxidation chemistry of perfluoroalkyl substances (PFAS). In particular, unimolecular dissociation reactions within unbranched -perfluoroalkyl chains, and their corresponding reverse barrierless association reactions, are expected to be significant contributors to the gas-phase thermal decomposition of families of species such as perfluorinated carboxylic acids and perfluorinated sulfonic acids. Unfortunately, experimental data for these reactions are scarce and uncertain.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!