Abstract-Concentrations of brominated flame retardants (BFRs), including polybrominated diphenylethers (PBDEs) and hexabromocyclododecane (HBCD), were investigated in an arctic marine food chain consisting of four invertebrate species: polar cod (Boreogadus saida), ringed seals (Pusa hispida), and polar bears (Ursus maritimus). The most abundant BFR, brominated diphenyl ether (BDE)-47, was found in detectable concentrations even in zooplankton, the lowest trophic level examined in this study. Most of the investigated BFRs biomagnified as function of tropic level in the food chain. A noticeable exception occurred at the highest trophic level, the polar bear, in which only BDE-153 was found to increase from its main prey, the ringed seal, indicating that polar bears appear to be able to metabolize and biodegrade most BFRs. In contrast, lower-brominated PBDEs, particularly BDE-47, showed clear signs of bioaccumulation in zooplankton, polar cod, and ringed seals. We suggest that this discrepancy in the fate of BFRs among the different species may be related to greater induction of oxidative detoxification activities in the polar bear. Absorption and debromination rates may be more important for bioaccumulation rates of BFRs in zooplankton, polar cod, and ringed seals. Lipid weight-based concentrations (LWCs) and whole body-based concentrations (WBCs) of BFRs were used to assess biomagnification factors (BMFs). Whole-body concentrations gave the most realistic BMFs, as BMFs derived from LWCs seem to be confounded by the large variability in lipid content of tissues from the investigated species. This study demonstrates that PBDEs and HBCD have reached measurable concentrations even in the lower trophic levels (invertebrates and fish) in the Arctic and biomagnifies in the polar bear food chain.

We studied the relationships between polychlorinated biphenyls (PCBs) and thyroid hormones (THs) and retinol within two groups of female polar bears (

Due to the extremely high affinity of selenium (Se) to mercury (Hg), Se sequesters Hg and reduces its biological availability in organisms. However the converse is also true. Hg sequesters Se, causing Hg to inhibit the formation of Se dependent enzymes while supplemental Se supports their continued synthesis. Hence, whether or not toxic effects accompany exposure to Hg depends upon the tissue Se:Hg molar ratio of the organism. The main objective of the present study was to investigate how levels of Hg and Se affected metallothionein (MT) induction in free-ranging brown trout, Salmo trutta, from Lake Mjøsa, Norway (a Se depauperate lake). MT is proposed as a sensitive biomarker of potential detrimental effects induced by metals such as Hg. Emphasis was addressed to elucidate if increased tissue Se:Hg molar ratios and Se levels affected the demands for MT in the trout. The Se:Hg molar ratio followed by tissue Se levels were most successful for assessing the relationship between metal exposure and MT levels in the trout. Thus, Hg in molar excess over Se was a stronger inducer of MT synthesis than tissue Hg levels in the trout, supporting the assumption that Se has a prominent protective effect against Hg toxicity. Measuring Hg in animals may therefore provide an inadequate reflection of the potential health risks to humans and wildlife if the protective effects of Se are not considered.

Space-use was examined in 54 female polar bears (Ursus maritimus) from Svalbard and the Barents Sea that were collared with satellite transmitters to provide information on their spatial positions and annual home range sizes. Plasma samples from the same animals were analyzed for concentrations of six relevant PCB congeners (PCB-99, -153, -156, -180, -194, and -118). Factors related to space-use strategy (such as home range size; annual, spring, and winter longitudinal position; and spring and summer latitudinal position) were important determinants of PCB concentrations in plasma. In addition, reproductive status of the polar bears and plasma lipid content affected PCB concentrations. Among the tested variables, annual home range size was the variable that affected sigmaPCB5 (sum of PCB-99, -153, -156, -180, and -194) to the largest degree (r2 = 0.22). We propose that the positive effect of home range size on sigmaPCB5 in female polar bears is related to the higher energetic costs required to occupy large home range sizes as compared to small home range sizes. Polar bears with large home range sizes would need to consume more prey than bears with small home range sizes, and increased feeding without a change in elimination of persistent compounds can explain their higher sigmaPCB5 concentrations. Polar bears with large home range sizes were also more pelagic, inhabiting areas further east, closer to the ice-edge zone than animals with small home range sizes. Thus, prey choice associated with a pelagic space-use strategy may also explain the higher sigmaPCB5 in polar bears with large home range sizes.

BackgroundConcentrations of brominated flame retardants (BFRs) are reported to increase in marine ecosystems.ObjectivesCharacterize exposure to BFRs in animals from different trophic levels in North-East Atlantic coastal marine ecosystems along a latitudinal gradient from southern Norway to Spitsbergen, Svalbard, in the Arctic. Calanoid species were collected from the Oslofjord (59°N), Froan (64°N), and Spitsbergen (> 78°N); Atlantic cod (Gadus morhua) from the Oslofjord and Froan; polar cod (Boreogadus saida) from Bear Island (74°N) and Spitsbergen; harbor seal (Phoca vitulina) from the Oslofjord, Froan, and Spitsbergen; and ringed seal (Phoca vitulina) from Spitsbergen. Eggs of common tern (Sterna hirundo) were collected from the Oslofjord, and eggs of arctic terns (Sterna paradisaea) from Froan and Spitsbergen.ResultsLevels of polybrominated diphenylethers (PBDEs) and hexabromocyclododecane (HBCD) generally decreased as a function of increasing latitude, reflecting distance from release sources. The clear latitudinal decrease in levels of BFRs was not pronounced in the two tern species, most likely because they are exposed during migration. The decabrominated compound BDE-209 was detected in animals from all three ecosystems, and the highest levels were found in arctic tern eggs from Spitsbergen. HBCD was found in animals from all trophic levels, except for in calanoids at Froan and Spitsbergen.ConclusionsEven though the levels of PBDEs and HBCD are generally low in North-East Atlantic coastal marine ecosystems, there are concerns about the relatively high presence of BDE-209 and HBCD.

Organochlorine pollutants (OCs), such as polychlorinated biphenyls (PCBs), DDT, chlordanes (CHLs), hexachlorobenzene (HCB) and hexachlorocyclohexanes (HCHs) were determined in blubber biopsies from free-ranging Baltic and Atlantic gray seal (Halichoerus grypus) pups. Well-fed pups from the Baltic Sea had concentrations of DDT, PCBs, and HCHs that were 2 to 10 times higher than in corresponding pups from populations in the Atlantic Ocean. The OC pattern in the Baltic seals differed significantly from that of their Atlantic relatives, reflecting the predominance of regional point source inputs into the Baltic Sea and long-range atmospheric inputs into the Atlantic Ocean. The differences in the pattern of the compounds also indicated an enhanced metabolism of the more metabolizable compounds in the more contaminated Baltic seals. Surprisingly, the proportions of the high chlorinated and low-volatile PCB congeners (> 6 Cl atoms) were comparable or lower in the Baltic pups as compared to the Atlantic pups. This difference might be due to Baltic seals occupying a lower trophic level than Atlantic seals and/or to the eutrophication situation in the Baltic Sea, which causes sedimentation of these PCB congeners. Significantly higher OC concentrations were found in starved and/or abandoned Baltic pups as compared to well-fed pups. The most contaminated Baltic seal pups in the present study had PCB concentrations that are comparable or higher than those reported to impair the immune systems and vitamin A dynamics in phocids.

Marine apex predators, such as the gray seal (Halichoerus grypus), are exposed to high concentrations of organochlorine (OC) compounds via biomagnification in the food web. These lipophilic pollutants are transferred from the female to her offspring during lactation, and there is particular concern for endocrine disruption in the offspring. Herein we examined associations between the blubber concentrations of polychlorinated biphenyls (PCBs), dichlorodiphenyltrichloroethane (DDT) and metabolites, chlordanes, hexachlorocyclohexanes (HCHs) and hexachlorobenzene (HCB), and plasma concentrations of thyroid hormones (thyroxine [T4] and tri-iodothyronine [T3]) in free-ranging, newly weaned gray seal pups from the Baltic Sea and the Norwegian waters of the Atlantic Ocean. Concentrations of total T3 (TT3) and free T3 (FT3) were significantly lower in the polluted seals from the Baltic Sea. Blubber concentrations of the sum of the analyzed PCB congeners (sigmaPCBs) and the sum of the DDT compounds (sigmaDDTs) were correlated negatively with plasma TT3 and FT3 concentrations. The results from this study indicate that OCs may affect levels of thyroid hormones in free-ranging gray seal pups, and that more focus should be put on T3 when addressing the possible effects of OCs on thyroid hormone function and status in nonrodent species.

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