Persistent organic pollutants (POPs) in killer whales (Orcinus orca) from the Crozet Archipelago, southern Indian Ocean

Persistent organic pollutants (POPs), including polychlorinated biphenyls (PCBs), polychlorinated dibenzo-p-dioxins (PCDDs), and dibenzofurans (PCDFs), are ubiquitous environmental contaminants of which significant concentrations are reported in upper trophic level animals. In 1998, we collected blubber biopsy samples (n = 11) from killer whales (Orcinus orca) inhabiting the coastal waters around Possession Island, Crozet Archipelago, southern Indian Ocean, for contaminant analyses. Despite inhabiting an isolated region far removed from industrial activities, these killer whales can presently be considered among the most PCB-contaminated cetaceans in the southern hemisphere, with concentrations ranging from 4.4 to 20.5 mg/kg lipid weight (lw). PCDD levels ranged from below the detection limit (5 ng/kg) to 77.1 ng/kg lw and PCDF levels from below the detection limit (7 ng/kg) to 36.1 ng/kg lw. Over 70% of our study animals had PCB concentrations which exceeded a 1.3 mg/kg PCB threshold established for endocrine disruption and immunotoxicity in free-ranging harbour seals, suggesting that organic contaminants cannot be ruled out as an additional threat to this declining population.     

Polystyrene nanoplastics aggravated ecotoxicological effects of polychlorinated biphenyls in on zebrafish (Danio rerio) embryos

In view of the accumulation of nanoplastics (NPs) in the food chain of environment and animals, and the good adsorption properties of nano-plastics to toxic substances, it is necessary to explore the influence of NPs in living organisms. In this study, single and joint toxicological effects of polystyrene nanoplastics (PS-NPs, size 80 nm) and polychlorinated biphenyls (PCBs), were explored in freshwater aquatic animal model zebrafish (Danio rerio). Our study found that exposure to single PS-NPs induced mild acute toxicity, albeit the combined exposure of PS-NPs and polychlorinated biphenyls aggravated the toxicity of PCBs in a dose-dependent manner. Results from gene expression profiling showed that NPs exposure could activate detoxification process, resulting in a slight up-regulation of antioxidant genes (sod1, gstp1), bone development genes (bmp2, bmp4) and cardiac gene (tbx20); while PCBs suppressed the detoxification through down-regulation of these genes, and the addition of NPs will exacerbate the impact of PCBs on gene suppression. Importantly, the results of in vivo purification experiments found that NPs showed prolonged retention in liver, intestine and gills of zebrafish and they might have crossed biological barrier and accumulate in lipid-rich tissues and excretion does not appear as the significant pathway for their elimination. In conclusion, the toxic effects of polychlorinated biphenyls on chorionic protected embryos were not significant as zebrafish chorion plays an important role in resisting the invasion of pollutants; PCBs can seriously damage the bone and heart development of zebrafish, while the presence of NPs significantly enhanced the toxicity of PCBs in zebrafish, which is an alarming concern for growing NPs levels and ecological safety in aquatic environment.     

Specific profiles of polybrominated diphenylethers (PBDEs) and polychlorinated biphenyls (PCBs) in fish and tucuxi dolphins from the estuary of Paraíba do Sul River, Southeastern Brazil

Polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) are ubiquitous pollutants in the environment and subject of several studies due to their adverse effects as endocrine disruptors. Despite the concern over widespread distribution of PBDEs even in sparsely populated regions of the world, few studies have reported their occurrence in Brazil. In this study, PBDEs and PCBs levels were measured in selected fish species and dolphins from Paraiba do Sul River, Brazil. BDE 47 and 85 were the predominant congeners. Low chlorinated congeners showed the highest concentrations in fish; however dolphins presented the highest proportion of PCBs 153, followed by 138 and 180. The daily intake of PBDEs and PCBs was estimated for the population of this region. PCB daily intake through consumption of croaker was above the limits set by the Brazilian Ministry of Agriculture, raising great concern over the existence of a source of PCB contamination in Brazil.     

Largemouth bass (Micropterus salmoides) and striped mullet (Mugil cephalus) as vectors of contaminants to human consumers in northwest Florida

The health benefits of regular consumption of fish and seafood have been espoused for many years. However, fish are also a potential source of environmental contaminants that have well known adverse effects on human health. We investigated the consumption risks for largemouth bass (Micropterus salmoides; n = 104) and striped mullet (Mugil cephalus; n = 170), two commonly harvested and consumed fish species inhabiting fresh and estuarine waters in northwest Florida. Skinless fillets were analyzed for total mercury, inorganic arsenic, polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/F), polychlorinated biphenyls (PCBs), and organochlorine pesticides. Contaminant levels were compared to screening values (SV) calculated using U.S. Environmental Protection Agency (EPA) recommendations for establishing consumption advisories. Largemouth bass were found to contain high levels of total mercury at all sampling locations (0.37–0.89 ug/g) and one location exhibited elevated total PCBs (39.4 ng/g). All of the samples exceeded Florida fish consumption advisory trigger levels for total mercury and one location exceeded the U.S. EPA SV for total PCBs. As a result of the high mercury levels, the non-cancer health risks (hazard index–HI) for bass were above 1 for all locations. Striped mullet from several locations with known point sources contained elevated levels of PCBs (overall range 3.4–59.3 ng/g). However, total mercury levels in mullet were low. Eight of the 16 mullet sampling locations exceeded the U.S. EPA SV for total PCBs and two locations exceeded an HI of 1 due to elevated PCBs. Despite the elevated levels of total PCBs in some samples, only two locations exceeded the acceptable cancer risk range and therefore cancer health risks from consumption of bass and mullet were determined to be low at most sampling locations.     

An 80‐year record of sediment quality in the lower Mississippi River

In 1937, the US Army Corps of Engineers cut through the “neck” of a large meander on the lower Mississippi River (below the confluence with the Ohio River) forming the Caulk Neck cutoff and creating Lake Whittington, a 26‐km long oxbow lake, in northern Mississippi. Since 1938, seasonal flooding and a boat channel connecting the lake with the Mississippi River have led to sediment accumulation in the lake, resulting in an 80‐year record of sediment quality in the river. On the basis of an age‐dated sediment core from the lake, trends in trace metals and hydrophobic organic compounds (except polycyclic aromatic hydrocarbons) follow well‐known patterns with upward trends from the 1930s to the ca 1970s, followed by downward trends to the present. Two factors contribute to these patterns: reservoir construction and changes in emissions. The construction of seven large reservoirs on the Missouri River, in particular the closure of the Fort Randall (1953) and Gavins Point (1955) Dams, greatly reduced the load of relatively clean sediment to the Mississippi River, likely contributing to downstream increases in contaminant concentrations in the Mississippi River. Increasing anthropogenic emissions also contributed to upward trends until ca 1970 when major environmental policy actions began resulting in broad decreases in emissions and downward trends in the concentrations of most of the contaminants monitored. Polycyclic aromatic hydrocarbons and phosphorus are partial exceptions to this pattern, with increases to the 1960s and variable concentrations showing no clear trend since. Published 2012. This article is a U.S. Government work and is in the public domain in the USA.     

莱州湾及东营近岸海域生物体中有机氯农药 和多氯联苯污染状况与风险评价

2011年5月采集莱州湾及东营近岸海域鱼、贝、甲壳(蟹、虾)、头足四类235个生物体样品, 用气相色谱法测定其中六六六(HCHs)、滴滴涕(DDTs)及多氯联苯(PCBs)含量, 对其残留水平、分布、组成特征及污染源进行分析, 对污染现状及人体健康风险进行了评价。结果表明, 研究海域生物体中HCHs含量(湿重) N.D.—5.73?g/kg; DDTs含量(湿重) 0.122—304?g/kg; PCBs含量(湿重) N.D.—6.51?g/kg。根据各同分异构体百分比组成分析, 莱州湾及东营近岸海域近期无新的大面积HCHs、DDTs污染输入。与同类研究相比, 莱州湾及东营近岸海域生物体PCBs含量处于较低水平, 而HCHs和DDTs含量处于中间水平。通过污染指数分析得出: 所有生物体HCHs、PCBs均未受到污染; 55%生物体DDTs受到不同程度污染。研究海域生物体HCHs、DDTs、PCBs含量低于各国食品安全限量; 以美国环保局推荐方法评价本海域生物体HCHs、PCBs食用致癌风险为可接受风险, 但是DDTs含量存在一定的致癌风险。     

Distribution characteristics of polychlorinated biphenyls （PCBs） in coastal areas of Okinawa Island, Japan

Surface sediment and seawater samples were collected from coastal areas around Okinawa Island from September 2001 to May 2002. The samples were analyzed for total polychlorinated biphenyl (PCB) levels and homolog composition. The results show that total PCB levels ranged from 0.32 to 128.7 ng/g (dry wt.) in sediment and 1.59 to 2.48 ng/L in seawater. The levels exceed the Environmental Quality Standard (EQS) for water pollution of Japan. The distribution of PCB homolog showed different patterns in the sediments and seawaters. Penta-chlorobiphenyls (CBs) comprised the main congener group in seawater, while hexa-CBs were more abundant homologs in the sediments. The heavily contaminated sites featured higher CBs, including penta-CBs, hexa-CBs, and hepta-CBs, than those in less contaminated sites where tri-CBs dominated. This study provides current distribution and geochemical behavior of PCBs in the coastal areas around Okinawa Island.     

Historical trends of organic pollutants in sediment cores from Hong Kong

Recent studies have indicated the occurrence of a wide range of trace organic contaminants, including polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) in the Hong Kong environment. These contaminants are potentially harmful to ecological systems, particularly in coastal areas. In this study, two sediment cores (4m) were collected from southern waters of Hong Kong in 2004 to study the historical trends, distribution patterns, and potential sources of trace organic contaminants. DDTs (p,p'-DDT, o,p'-DDT, p,p'-DDD, o,p'-DDD and p,p'-DDE), hexachlorohexanes (HCHs) (alpha and gamma), hexachlorobenzene (HCB), and PCBs were detected in the samples, whereas other target compounds were all below detection limits. Many OCPs have not been produced or used for many years due to toxicological or environmental concerns and PCB use is prohibited in Hong Kong. However, some compounds were still detectable in recent years, and were found to be widely distributed in the environment, likely because of pollutant inputs from the highly industrialized Pearl River Delta region. These results provide important information on current and historical contamination in Hong Kong, and help to reconstruct the pollution history of these trace organic pollutants in Hong Kong coastal waters.     

Biomagnification profiles of polycyclic aromatic hydrocarbons, alkylphenols and polychlorinated biphenyls in Tokyo Bay elucidated by δC and δN isotope ratios as guides to trophic web structure

Biomagnification profiles of polycyclic aromatic hydrocarbons (PAHs), alkylphenols, and polychlorinated biphenyls (PCBs) from the innermost part of Tokyo Bay, Japan were analyzed using stable carbon (δ¹³C) and nitrogen (δ¹⁵N) isotope ratios as guides to trophic web structure. δ¹⁵N analysis indicated that all species of mollusks tested were primary consumers, while decapods and fish were secondary consumers. Higher concentrations of PCBs occurred in decapods and fish than in mollusks. In contrast, concentrations of PAHs and alkylphenols were lower in decapods and fish than in mollusks. Unlike PCBs, whose concentrations largely increased with increasing δ¹⁵N (i.e. increasing trophic level), all PAHs and alkylphenols analyzed followed a reverse trend. Molecular weights of PAHs are lower than those of PCBs, therefore low membrane permeability caused by large molecular size is an unlikely factor in the “biodilution” of PAHs. Organisms at higher trophic levels may rapidly metabolize PAHs or they may assimilate less of them.