RESUMO
Fish consumption is an important source of human exposure to heavy metals. To determine the health risks for metals by consumption of marine fish in China, three species of fish, namely large yellow croaker (Pseudosciaena crocea), small yellow croaker (Pseudosciaena polyactis) and silver pomfret (Pampus argenteus) were collected and analyzed for methylmercury (MeHg), total mercury (T-Hg), selenium, cadmium, cobalt, chromium, copper, iron, manganese, nickel, lead, strontium and zinc. The large yellow croakers had the highest concentrations of mercury, lead, nickel and zinc, and the levels of MeHg were positively correlated to T-Hg. The ratios of MeHg to T-Hg in yellow croakers were significantly higher than those in silver pomfret, indicating differences in accumulation and magnification of MeHg in these two types of fish. The concentration of T-Hg was found to decrease as the Se level in fish tissues increased. Cadmium levels in 16% of the samples were higher than the criterion recommended by the European Commission Regulation. The concentrations of other metals were well below international standards. A human health risk assessment showed that the estimated daily intake of these metals did not exceed the reference dose established by the US Environmental Protection Agency. The hazard quotients (HQs) were all less than 1, indicating a situation of no risk for consumption of these fish.
Assuntos
Contaminação de Alimentos/análise , Metais Pesados/análise , Compostos de Metilmercúrio/análise , Perciformes , Animais , China , Monitoramento Ambiental , Humanos , Músculos/química , Medição de RiscoRESUMO
Muscle tissues of large yellow croakers (Pseudosciaena crocea) and sliver pomfret (Pampus argenteus) from nine coastal cities of East China including Dalian, Tianjin, Qingdao, Shanghai, Zhoushan, Wenzhou, Fuzhou, Quanzhou and Xiamen were analyzed for polychlorinated biphenyl (PCB) concentrations. Thirty-six PCB congeners were quantified in the fishes, of which 11 congeners were dioxin-like PCBs. The total PCB concentrations of the present study were at the low end of the global range, which may be related to the smaller usage and shorter consumption history of PCBs in China. PCBs 18, 29, 52, 66, 101, 104, 138, 153, 180 and 194 were the major constituents found in the fish samples. Regression analysis showed a strong positive correlation (R(2)=0.800; p<0.001) between total dioxin-like PCBs and total PCB concentrations, and that total PCB concentrations explain 80% of the variability in total dioxin-like PCB concentrations. Among the species investigated, significantly higher concentrations of total PCBs were found in croakers than in pomfrets, which may be attributed to their different feeding and living habits. No significant difference in total PCB concentrations among the cities was observed; principal component analysis (PCA) of PCB profiles indicated that PCB pollution came from similar sources in the sampling areas and that there may be other PCB sources in Dalian and Wenzhou. The calculated carcinogenic risks (CRs) from the two species based on a low consumption group and high consumption group were all greater than 10(-6), suggesting that daily exposure to dioxin-like PCBs via fish consumption results in a lifetime cancer risk of greater than one in one million. In contrast, the hazard quotients (HQs) of noncancer risks were all less than unity.
Assuntos
Perciformes , Bifenilos Policlorados/análise , Medição de Risco , Animais , China , Exposição Ambiental , Contaminação de Alimentos/análise , Humanos , Músculos/química , Análise de Componente PrincipalRESUMO
This study reports concentrations of hexabromocyclododecanes (HBCDs) in two species of marine fish, large yellow croaker (Pseudosciaenacrocea) and silver pomfret (Pampusargenteus) (n = 46), from nine Chinese coastal cities (Dalian, Tianjin, Qingdao, Shanghai, Zhoushan, Wenzhou, Fuzhou, Quanzhou and Xiamen). HBCDs were detectable in all samples analyzed, indicating ubiquitous contamination of these compounds in the Chinese coastal environment. The average total HBCD concentration was 3.7 ng g⻹ lipid weight (range: 0.57-10.1 ng g⻹ lipid weight), which is relatively lower than other regions of the world, especially Europe, where HBCDs are intensively used. Among the three individual HBCD isomers (α-, ß- and γ-HBCD) in all fish samples, the α-isomer showed a remarkable predominance (from 87.5% to 100% of total contribution), indicating its higher bioaccumulative potential. Geographically, the highest HBCD level present in fish was found in Dalian in northern China, and the lowest occurred in Wenzhou. Estimated daily intakes of HBCDs via fish consumption for the Chinese population were 0.004-1.00 ng kg body weight⻹ d⻹. These exposure levels were much lower than the effect levels.
Assuntos
Retardadores de Chama/metabolismo , Hidrocarbonetos Bromados/metabolismo , Perciformes/metabolismo , Poluentes Químicos da Água/metabolismo , Animais , China , Exposição Ambiental/análise , Exposição Ambiental/estatística & dados numéricos , Humanos , Alimentos Marinhos/estatística & dados numéricos , Poluição Química da Água/estatística & dados numéricosRESUMO
Concentrations of polybrominated diphenyl ethers (PBDEs) in yellow croakers (Pseudosciaena crocea) and silver pomfrets (Pampus argenteus) collected from nine coastal cities along the eastern China coastline were investigated. PBDE congeners with mono- to hexa-brominated substitutions were detected in the samples, indicating their ubiquitous distribution in the marine environment of China. The total PBDE concentration averaged 3.04 ng g⻹ lipid wt, a level that was relatively lower than in other regions of the world, especially North America where Penta-BDE was extensively used. Geographically, the highest concentration of PBDEs was found in Xiamen, and the PBDE levels in yellow croakers were significantly higher than those in pomfrets in most of the selected cities, a pattern which may be related to the different feeding habits of the two species. The congener profiles of PBDEs were found to be different from the commonly detected pattern in fishes from other regions of the world (i.e., BDE47>BDE99, BDE100>BDE153, BDE154). BDE47 and BDE154 were the predominant congeners in both species, accounting for more than 60% of the total PBDE concentrations. The reasons for the relatively high proportion of BDE154 may be due to the debromination of higher brominated congeners such as BDE183 and BDE209 by these two species.
Assuntos
Monitoramento Ambiental , Éteres Difenil Halogenados/metabolismo , Perciformes/metabolismo , Poluentes Químicos da Água/metabolismo , Animais , China , Músculos/metabolismo , Bifenil Polibromatos/metabolismoRESUMO
From July to September 2008, air samples were collected aboard the research expedition icebreaker XueLong (Snow Dragon) as part of the 2008 Chinese Arctic Research Expedition Program. Hexachlorocyclohexane (HCH) concentrations were analyzed in all of the samples. The average concentrations (± standard deviation) over the entire period were 33 ± 16, 5.4 ± 3.0, and 13 ± 7.5 pg m⻳ for α-, ß- and γ-HCH, respectively. Compared to previous studies in the same areas, total HCH (ΣHCH, the sum of α-, ß-, and γ-HCH) levels declined by more than 10 × compared to those observed in the 1990s, but were approximately 4 × higher than those measured by the 2003 China Arctic Research Expedition, suggesting the increase of atmospheric ΣHCH recently. Because of the continuing use of lindane, ratios of α/γ-HCH showed an obvious decrease in North Pacific and Arctic region compared with those for 2003 Chinese Arctic Research Expedition. In Arctic, the level of α-HCH was found to be linked to sea ice distribution. Geographically, the average concentration of α-HCH in air samples from the Chukchi and Beaufort Seas, neither of which contain sea ice, was 23 ± 4.4 pg m⻳, while samples from the area covered by seasonal ice (â¼75°N to â¼83°N), the so-called "floating sea ice region", contained the highest average levels of α-HCH at 48 ± 12 pg m⻳, likely due to emission from sea ice and strong air-sea exchange. The lowest concentrations of α-HCH were observed in the pack ice region in the high Arctic covered by multiyear sea ice (â¼83°N to â¼86°N). This phenomenon implies that the re-emission of HCH trapped in ice sheets and Arctic Ocean may accelerate during the summer as ice coverage in the Arctic Ocean decreases in response to global climate change.