PCB residues in the tissues of sea ducks wintering on the south coast of the Baltic Sea, Poland

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Abstract

The Baltic Sea is known to be severely polluted by a range of chemicals, one group of which being PCBs. Although the use and production of PCBs were limited or banned in many countries in the 1970s, their presence is still observed in the environment. The aim of this study was to evaluate PCBs concentration in four species of diving sea ducks, interspecies and tissues differences, and in the case of game species, comparison of the obtained results with maximal residue levels (MRLs) and tolerable weekly intake (TWI). The level of Σi-PCBs was noted in most examined samples (liver, muscle, fat tissue) at levels ranging between < LoD and 2315.45 ng/g lw. The dominant congener was PCB 153, followed by PCB 180 and 138. The mean dl-PCB-TEQ value in the muscles of the tested tufted ducks and common pochards was 0.31 and 0.71 pg-TEQ/g lw, respectively, which is 8–25 and 18–57% of the TEQ maximum limit (ML) value for farm animal muscles. The average decrease in i-ΣPCB concentration in the fat tissue of ducks wintering in the Baltic Sea southern coast was found to be 2.9–3.3%/year. The analysis of PCB residues indicates that the common pochard and tufted duck are not suitable for consumption due to high Σi-PCB concentrations. However, the regular consumption of muscle and liver of game birds does not result in an unacceptable intake of dl-PCBs, i.e., above the TWI value.

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The 2005 World Health Organization reevaluation of human and Mammalian toxic equivalency factors for dioxins and dioxin-like compounds.

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In June 2005, a World Health Organization (WHO)-International Programme on Chemical Safety expert meeting was held in Geneva during which the toxic equivalency factors (TEFs) for dioxin-like compounds, including some polychlorinated biphenyls (PCBs), were reevaluated. For this reevaluation process, the refined TEF database recently published by Haws et al. (2006, Toxicol. Sci. 89, 4-30) was used as a starting point. Decisions about a TEF value were made based on a combination of unweighted relative effect potency (REP) distributions from this database, expert judgment, and point estimates. Previous TEFs were assigned in increments of 0.01, 0.05, 0.1, etc., but for this reevaluation, it was decided to use half order of magnitude increments on a logarithmic scale of 0.03, 0.1, 0.3, etc. Changes were decided by the expert panel for 2,3,4,7,8-pentachlorodibenzofuran (PeCDF) (TEF = 0.3), 1,2,3,7,8-pentachlorodibenzofuran (PeCDF) (TEF = 0.03), octachlorodibenzo-p-dioxin and octachlorodibenzofuran (TEFs = 0.0003), 3,4,4',5-tetrachlorbiphenyl (PCB 81) (TEF = 0.0003), 3,3',4,4',5,5'-hexachlorobiphenyl (PCB 169) (TEF = 0.03), and a single TEF value (0.00003) for all relevant mono-ortho-substituted PCBs. Additivity, an important prerequisite of the TEF concept was again confirmed by results from recent in vivo mixture studies. Some experimental evidence shows that non-dioxin-like aryl hydrocarbon receptor agonists/antagonists are able to impact the overall toxic potency of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and related compounds, and this needs to be investigated further. Certain individual and groups of compounds were identified for possible future inclusion in the TEF concept, including 3,4,4'-TCB (PCB 37), polybrominated dibenzo-p-dioxins and dibenzofurans, mixed polyhalogenated dibenzo-p-dioxins and dibenzofurans, polyhalogenated naphthalenes, and polybrominated biphenyls. Concern was expressed about direct application of the TEF/total toxic equivalency (TEQ) approach to abiotic matrices, such as soil, sediment, etc., for direct application in human risk assessment. This is problematic as the present TEF scheme and TEQ methodology are primarily intended for estimating exposure and risks via oral ingestion (e.g., by dietary intake). A number of future approaches to determine alternative or additional TEFs were also identified. These included the use of a probabilistic methodology to determine TEFs that better describe the associated levels of uncertainty and "systemic" TEFs for blood and adipose tissue and TEQ for body burden.

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Organochlorine (OC) pesticides and the more persistent polychlorinated biphenyls (PCBs) have well-established dose-dependent toxicities to birds, fish and mammals in experimental studies, but the actual impact of OC pollutants on European marine top predators remains unknown. Here we show that several cetacean species have very high mean blubber PCB concentrations likely to cause population declines and suppress population recovery. In a large pan-European meta-analysis of stranded (n = 929) or biopsied (n = 152) cetaceans, three out of four species:- striped dolphins (SDs), bottlenose dolphins (BNDs) and killer whales (KWs) had mean PCB levels that markedly exceeded all known marine mammal PCB toxicity thresholds. Some locations (e.g. western Mediterranean Sea, south-west Iberian Peninsula) are global PCB “hotspots” for marine mammals. Blubber PCB concentrations initially declined following a mid-1980s EU ban, but have since stabilised in UK harbour porpoises and SDs in the western Mediterranean Sea. Some small or declining populations of BNDs and KWs in the NE Atlantic were associated with low recruitment, consistent with PCB-induced reproductive toxicity. Despite regulations and mitigation measures to reduce PCB pollution, their biomagnification in marine food webs continues to cause severe impacts among cetacean top predators in European seas.

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The polychlorinated biphenyls (PCBs) are synthetic organochlorine chemicals that were useful industrial products in the past, but their production was ended because they persist in both the environment and living organisms. The PCBs are mixtures of up to 209 different components (congeners), depending on the number and position of chlorines around the biphenyl ring. The PCBs are fat-soluble substances to which everyone is exposed through ingesting animal fats, inhalation, or dermal contact. Exposure to PCBs suppresses the immune system, thereby increasing the risk of acquiring several human diseases. Both ortho-substituted and coplanar (dioxin-like) congeners are tumor promoters that enhance the effects of other carcinogenic substances. PCB exposure, especially during fetal and early life, reduces IQ and alters behavior. The PCBs alter thyroid and reproductive function in both males and females and increase the risk of developing cardiovascular and liver disease and diabetes. Women are at high risk of giving birth to infants of low birth weight, who are at high lifetime risk for several diseases. As knowledge of their toxic effects has grown faster than environmental levels have declined, PCBs remain dangerous contaminants.

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Author and article information

Contributors

Agnieszka Tomza-Marciniak:

ORCID: http://orcid.org/0000-0002-3803-7058

(+48)914496792 , agnieszka.tomza-marciniak@zut.edu.pl

Journal

Journal ID (nlm-ta): Environ Sci Pollut Res Int

Journal ID (iso-abbrev): Environ Sci Pollut Res Int

Title: Environmental Science and Pollution Research International

Publisher: Springer Berlin Heidelberg (Berlin/Heidelberg )

ISSN (Print): 0944-1344

ISSN (Electronic): 1614-7499

Publication date (Electronic): 22 February 2019

Publication date PMC-release: 22 February 2019

Publication date (Print): 2019

Volume: 26

Issue: 11

Pages: 11300-11313

Affiliations

[1 ]ISNI 0000 0001 0659 0011, GRID grid.411391.f, Department of Animal Reproduction Biotechnology and Environmental Hygiene, , West Pomeranian University of Technology, Szczecin, ; Janickiego 29, 71-270 Szczecin, Poland

[2 ]ISNI 0000 0001 0659 0011, GRID grid.411391.f, Department of Toxicology, , West Pomeranian University of Technology, Szczecin, ; Papieża Pawła VI 3, 71-459 Szczecin, Poland

[3 ]ISNI 0000 0000 8780 7659, GRID grid.79757.3b, Department of Ecology and Environmental Protection, , University of Szczecin, ; Wąska 13, 71-415 Szczecin, Poland

[4 ]ISNI 0000 0001 0659 0011, GRID grid.411391.f, Department of Ruminant Science, , West Pomeranian University of Technology, Szczecin, ; Janickiego 29, 71-270 Szczecin, Poland

Author notes

Responsible editor: Roland Peter Kallenborn

Author information

Agnieszka Tomza-Marciniak http://orcid.org/0000-0002-3803-7058

Article

Publisher ID: 4586

DOI: 10.1007/s11356-019-04586-4

PMC ID: 6469621

PubMed ID: 30796664

SO-VID: 5fbf7167-0fab-4cc2-a41b-a4b01b8ac647

License:

OpenAccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.