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The Southern Yellow Sea (SYS) is an important reservoir of anthropogenic organic contaminants, such as polybrominated diphenyl ethers (PBDEs). To reconstruct the historical records of PBDEs and examine their relationships with the human activities and organic matters, a 210 Pb-dated sediment core was collected from the central mud area in the SYS. The concentrations of tri-to hepta-BDEs (∑ 7 PBDEs) and BDE-209 ranged from 9.8 to 99.8 pg g −1 d.w. and from 12.1 to 855.4 pg g −1 d.w., respectively, both displaying the increasing trends from the bottom to the surface. More importantly, there was a faster increase for PBDEs since the 1990s, especially for BDE-209, which responded well with the rapid economic growth, and the increases of urbanization and industrialization in the local areas of the SYS. The analogously vertical patterns and significant relationships between PBDEs and total organic carbon (TOC) implied the TOC-dependent deposition of PBDEs in the core. Furthermore, multiple biomarker-based proxies of terrestrial organic matter (TOM) and marine organic matter (MOM) were introduced to systematically investigate the different effects of TOM and MOM on PBDE deposition in the SYS. The similarly down-core profiles and significant correlations were found between PBDEs and the MOM proxies (sum of rassicasterol, dinosterol and C 37 alkenones (∑A + B + D) and marine TOC) as well as the branched and isoprenoid tetraether (BIT), but not for TOM proxies (∑C 27 +C 29 +C 31 n -alkanes, terrestrial and marine biomarker ratio (TMBR) and terrestrial TOC), indicating that MOM was an important factor driving PBDE deposition in the sediment core from the SYS. [ABSTRACT FROM AUTHOR]

The Southern Yellow Sea (SYS) is believed to be influenced by the contaminants from mainland China and the Korean peninsula. Here we report the first record about concentrations of polybrominated diphenyl ethers (PBDEs) in the sediments of the SYS. The concentrations of ∑ 7 PBDEs (BDE-28, 47, 99, 100, 153, 154, 183) and BDE-209 were 0.064–0.807 ng g −1 (dry weight) and 0.067–1.961 ng g −1 with a mean value of 0.245 ng g −1 and 0.652 ng g −1 , respectively. These are distinctively low compared with the PBDE levels previously reported in other regions of the world. PBDE concentrations gradually increased from the coastal areas to the central mud area. BDE-209 was the dominant congener, accounting for 70.2–91.6% of the total PBDEs. Congener profiles of PBDEs were similar to those in sediments from the Bohai Sea (BS), Laizhou Bay and modern Yellow River, which might be a tentative indication that they shared similar sources. Principal component analysis (PCA) revealed that PBDEs in the SYS were mainly from continental runoff (69.0%) and atmospheric deposition (31.0%). Depth profile of PBDEs in a sediment core collected from the edge of the central mud area showed that concentration of BDE-209 rapidly increased in recent years, which is in accordance with the replacement in demand and consumption of Penta- and Octa-BDEs by the Deca-BDE. Compared with BS, East China Sea, Erie and Ontario, the SYS was a relatively weak sink of PBDEs (0.102–1.288 t yr −1 for ∑ 7 PBDEs and 0.107–3.129 t yr −1 for BDE-209) in the world. [ABSTRACT FROM AUTHOR]

Congener profiles, distribution and sources of parent and alkyl-polycyclic aromatic hydrocarbons (PAHs) in surface sediments of Southern Yellow Sea (SYS), China were investigated. The ecological risk of parent-PAHs to aquatic organisms were evaluated based on sediment quality guidelines (SQGs), risk quotient (RQ), organic carbon (OC)-normalized analysis and mean effects range-median quotient (M-ERM-Q). The concentrations of 33 PAHs were analyzed, including 14 parent PAHs (without naphthalene and acenaphthylene), 16 alkyl-PAHs (7 methylphenanthrenes, 3 methylanthracenes, 3 methylfluoranthenes, and 3 methylpyrenes), dibenzothiophene, retene and perylene. Total concentrations of PAHs (TPAHs) ranged from 200.8 to 3629.0 ng/g dry weight (d.w.), with a mean value of 1035.4 ng/g d.w., and mainly contributed by fluorene, phenanthrene, methylphenanthrene, retene, fluoranthene and pyrene. Analysis of a broad variety of diagnostic ratios suggested that combustion was the key source of PAHs. Principal component analysis-multiple linear regression (PCA-MLR) indicated that combustion of coal, softwood and nature gas, coke oven, petroleum and vehicle emission were the main sources of PAHs in sediments of SYS, contributing 41.5%, 30.6%, 18.8%, and 9.0% to TPAHs, respectively. Ecological risk assessment of individual parent-PAHs suggested that fluorene, phenanthrene and fluoranthene may cause some risk to aquatic organisms in some stations. OC-normalized analysis and M-ERM-Q indicated that risk of multiple parent-PAHs was quite low in the studied area. [ABSTRACT FROM AUTHOR]