Organotropism of persistent organic pollutants and heavy metals in the Greenland shark Somniosus microcephalus in NE Greenland.

The Greenland shark Somniosus microcephalus is an opportunistic feeder, a top predator, and a very long-lived species. The brain, liver, red and white muscle, gonads, fat, skin, pancreas, and spleen of Greenland sharks from NE Greenland fjords were analysed for PCBs, PCDDs/DFs, PBDEs; DDT isomers; HCH isomers; dieldrin; endrin; HCB; Cd, Hg, Pb, and Se. PCBs (2.01-103 ng/g wet wt) and PBDEs (7.9-3050 pg/g wet wt) were detected in most of the samples. PCDDs/DFs showed high values when detected. DDTs, HCB and HCHs were only detected in some tissues. The ΣTEQ was 5.76 pg/g in muscle. Cadmium mainly accumulated in the pancreas and liver (19.6 and 10.7 mg/kg dry wt, respectively); mercury in red muscle (4.10-6.91 mg/kg dry wt); selenium in the pancreas (3.57 mg/kg dry wt) and spleen (1.95 mg/kg dry wt); lead in the skin (0.358 mg/kgd ry wt). The selenium-mercury ratio in the liver was also evaluated.

Biomarker responses in polar cod (Boreogadus saida) exposed to dietary crude oil.

Polar cod Boreogadus saida were exposed weekly to two doses of dietary crude oil for 4 weeks followed by 2 weeks of depuration. Administered doses corresponded on average to 4 and 9microgSigmaPAHsg(-1)fishweek(-1). Cytochrome P4501A1 (cyp1a1) and glutathione S-transferase (gst) mRNA expression, ethoxyresorufin O-deethylase (EROD) activity and metabolites in the bile showed strong and dose-dependent inductions at 2 and 4 weeks of exposure. Following 2 weeks depuration, mRNA expression of cyp1a1 and gst and PAH metabolites returned to basal levels while EROD activity and GST activity were still induced in the high oil treatment. The mRNA expressions of antioxidant defense genes (catalase, glutathione peroxidase and cytosolic and mitochondrial superoxide dismutase) did not change significantly during the experiment. Catalase activity was significantly depressed at week 2 in the high oil treatment. We conclude that the cyp1a1 mRNA expression, EROD activities and bile metabolites were the most reliable biomarkers of exposure while gst mRNA expression and GST activity were less sensitive and are considered only as complementary. Antioxidant defenses were poor biomarkers to assess effects of crude oil exposure in polar cod.

Biomarker responses in polar cod (Boreogadus saida) exposed to the water soluble fraction of crude oil.

In order to mimic the biological effects of an oil spill in Arctic waters, we examined several types of biomarkers (genes, enzymes, metabolites, and DNA damage) in polar cod Boreogadus saida experimentally exposed to the water soluble fractions of crude oil. During 4 weeks of exposure, induction of the studied biomarkers exceeded baseline levels. The mRNA expression of the cytochrome P4501A1 (cyp1a1) gene was the most promising biomarker, with glutathione S-transferase (gst) as a suitable complement. The delayed ethoxyresorufin O-deethylase (EROD) and GST activities and their persistence following 2 weeks of depuration may allow detection of previous exposures in field samples. The composition of PAH metabolites in the bile indicated the bioavailability of different PAH size-classes. Although mRNA expressions of antioxidant defense genes were induced at start of the exposure, with the strongest responses from catalase and cytosolic superoxide dismutase, they were poor for oil monitoring purposes due to their very short response times. Significant DNA damage demonstrated genotoxicity even at low PAH concentrations (<15microgL(-1)) and was correlated with benzo(a)pyrene and pyrene metabolites in the bile.

PAH biomarker responses in polar cod (Boreogadus saida) exposed to benzo(a)pyrene.

With expanding oil and gas activities into the Arctic region, there is a need to evaluate the induction capacity of polycyclic aromatic hydrocarbon (PAH) biomarkers on Arctic marine organisms and to test analytical methods that have been optimized for their temperate counterparts. Polar cod Boreogadus saida were injected intraperitoneally with cod liver oil (solvent control), 6.6+/-3.7, 85+/-48 or 378+/-190 microg kg(-1) wet weight of benzo(a)pyrene (B(a)P), or not injected (control), and liver and bile were sampled at 0 and 16 h and 1, 2, 4 and 7d. The mRNA expression of cytochrome P4501A1 (cyp1a1) and glutathione S-transferase (gst) genes showed a dose-dependent induction in the first 16 h following the injection and a return to basal levels after 4d. The aryl hydrocarbon receptor 2, however, showed no change in mRNA expression. The protein quantification of cytochrome P4501A (CYP1A), through Western blot analysis and the enzyme-linked immunosorbent assay (ELISA), presented similar but weaker and time-delayed responses (4-7d) compared to the gene (16 h to 2d). Ethoxyresorufin O-deethylase (EROD) and glutathione S-transferase (GST) activities increased significantly at day 7 following the gene induction and increase in protein levels. Overall, these biomarkers showed dose-dependent but weak responses to B(a)P and low levels of bile metabolites. The mRNA expressions of oxidative stress genes, superoxide dismutases (sod(Cu/Zn) and sod(Mn)), catalase (cat) and glutathione peroxidase (gpx), were all up-regulated between 16 h and 2d of B(a)P exposure with cat (72-fold) and sod(Cu/Zn) (20-fold) giving the strongest responses in the highest dose. Finally, CAT protein level and enzyme activities showed less clear responses than the genes. The mRNA expression showed the earliest responses, followed by the protein levels. The enzymatic activities were the least sensitive and responded to the exposure after 7d. The study shows the induction capability of biomarkers in polar cod at very low bioavailable doses of B(a)P and provides new information on the selected biomarkers for use in oil monitoring in the Arctic.