Biological markers of produced water (PW) exposure were studied in Atlantic cod (Gadus morhua) in both laboratory and field experiments, using authentic PW from a North Sea oil field. In the laboratory study, the PW exposure yielded significantly elevated levels of metabolites of polycyclic aromatic hydrocarbons (PAHs) and alkylphenols (APs) in bile even at the lowest exposure dose (0.125% PW). Other biomarkers (hepatic CYP1A induction and DNA adduct formation) responded at 0.25% and 0.5% PW concentrations. In the field study, bile metabolite markers and hepatic CYP1A were clearly increased in fish caged close to the PW outfall. Induction of plasma vitellogenin was not found in laboratory or field exposures, suggesting that the levels of oestrogen agonists (such as APs) might not have been sufficient to elicit induction, under the present conditions. The applicability of the biomarkers for use in water column biomonitoring programs is discussed.

Fish accumulate several trace elements in muscle, gills and liver, however studies also indicate that metals can be excreted through bile. Since metal contamination leads to modifications in bile composition, biliary excretion offers an alternative way to evaluate the presence of trace-elements. Bile is easier to obtain than other organs and presents a simpler matrix, making it easier for chemical pre-treatment. To verify if bile can be useful as a biomonitoring tool for metal contamination, liver and bile trace element concentrations were determined and correlated. The Artificial Neural Networks statistical technique was used to verify if liver trace-element quantification could be substituted by bile analysis. Results show that significant correlations were obtained between trace elements in bile and liver and the ANN validated the hypothesis that certain trace-elements in bile could be utilized instead of liver trace-elements. Further studies in this field are of interest to further validate this biomarker.

The objective of the present study was to investigate the short-term effects of benzo(a)pyrene (BaP) on juvenile sea bass (Dicentrarchus labrax L.) using a multiparameter approach. At the end of the 96 h of exposure to a range of BaP concentrations (2–256 μg l⁻¹) in laboratorial conditions, a suite of biomarkers involved in biotransformation pathways, oxidative stress and damage, neurotransmission and energetic metabolism were analysed. Levels of BaP metabolites in bile and BaP-type compounds in tissues were also included as biomarkers of exposure, and the post-exposure swimming velocity was used as a toxicity endpoint at a higher level of biological organisation. In addition, a time-series experiment on the levels of bile BaP metabolites was also performed. Increased levels of BaP metabolites in bile and BaP-type compounds in liver and brain of exposed fish were found, indicating BaP uptake, metabolisation and distribution by different tissues. BaP induced oxidative stress and damage, but no significant effects on the post-exposure swimming velocity, neurotransmission and energetic pathways were found. An increase in the levels of BaP metabolites in bile over time was also observed, reaching a threshold similar at all the concentrations tested. Overall, this integrative multiparameter study reflecting different biological responses of D. labrax was suitable to assess the effects caused by the short-term exposure to BaP and may be useful in the marine environmental risk assessment of polycyclic aromatic hydrocarbons pollution. The observed toxic effects also highlight the relevance of short-term exposure to relatively high concentrations of chemicals, as can occur in the case of punctual heavy chemical releases, such as oil spills in the marine environment.