Comparison of three techniques for administering radiolabeled substrates to sediments for trophic studies: uptake of label by harpacticoid copepods

Microbial grazing by two species of meiofaunal harpacticoid copepods (Heteropsyllus nunni and Thompsonula hyaenae) was determined by uptake of radioactive labels following their introduction into natural sediments from a low-energy intertidal site in Florida (29°5440N; 84°3130W) in May 1986. Grazing was related to three methods of radioactive-label introduction: injection, porewater replacement, and slurry. Uptake of label by harpacticoids was examined using two dual-label combinations, ³H-thymidine/¹⁴C-bicarbonate and ³H-thymidine/¹⁴C-acetate. The injection and porewater-replacement methods yielded statistically indistinguishable results. Results obtained by the slurry method differed significantly from the other two methods. We suggest that the unique results obtained in the slurry method were a consequence of the disruption of microbial-meiofaunal spatial relationships.     

Combining target analysis with sum parameters—a comprehensive approach to determine sediment contamination with PFAS and further fluorinated substances

Recent studies aiming at a fluorine mass balance analysis in sediments combined the determination of extractable organic fluorine (EOF) with target analysis. They reported high fractions of unidentified organic fluorine (UOF) compounds, as the target analysis covers only a limited number of per- and polyfluoroalkyl substances (PFAS). For this reason, in this study, a comprehensive approach was used combining target analysis with an extended PFAS spectrum, the EOF and a modified total oxidisable precursor (TOP) assay, which includes trifluoroacetic acid, to determine the PFAS contamination in sediments (n=41) and suspended solids (n=1) from water bodies in Northern Germany (Lower Saxony). PFAS are ubiquitous in the sediments (detected in 83% of the samples). Perfluorinated carboxylic acids (PFCAs) were found in 64% of the samples; perfluorinated sulfonic acids (PFSAs) were detected less frequently (21%), with the highest concentration observed for perfluorooctanesulfonic acid (PFOS). Levels of precursors and substitutes were lower. Applying the TOP assay resulted in an increase in PFCAs in 43% of the samples analysed. In most cases, target analysis and the TOP assay could not account for the EOF concentrations measured. However, as the fraction of UOF decreased significantly, the application of the TOP assay in fluorine mass balance analysis proved to be an important tool in characterising the PFAS contamination of riverine sediments.