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Polycyclic aromatic hydrocarbons (PAHs) were measured in 59 surface sediments from rivers in the Pearl River Delta and the northern continental shelf of the South China Sea. Total PAH concentrations varied from 138 to 6,793 ng/g dry weight. The sources of PAH inputs to sediments in the Pearl River Delta were qualitatively and quantitatively determined by diagnostic ratios and principal components analysis with multiple linear regression. The results showed that on average coal and wood combustion, petroleum spills, vehicle emissions, and nature sources contributed 36%, 27%, 25%, and 12% of total PAHs, respectively. Coal and biomass combustion was the main source of PAHs in sediments of the South China Sea, whereas petroleum combustion was the main source of pyrolytic PAHs in riverine and estuarine sediments of the Pearl River Delta. Perylene was formed in situ in river sediments and then transported to coastal areas along with other PAHs. The relative abundance of perylene from five-ring PAHs can be used to estimate the contribution of riverine-discharged PAHs to coastal sediments. [ABSTRACT FROM AUTHOR]

The present study provides information on the time trend of PBDEs in three sediment cores from the Pearl River Estuary (PRE), South China, using 210°Pb dating technique. The ∑PBDEs (except for BDE 209) concentrations in all sediment cores increased gradually from the bottom (mid-1970s) to the middle layer (later 1980s and early 1990s) followed by different temporal trends in different locations to the surface sediments, reflecting the variations in the consumption of commercial penta-BDEs mixture in different regions of the Pearl River Delta. The BDE 209 concentrations remained constant until 1990 and thereafter increased exponentially to the present, with doubling times of 2.6 ± 0.5–6.4 ± 1.6 years, suggesting the increasing market demands for deca-BDE mixture after 1990 in China. The inventories of ∑PBDEs and BDE 209 in sediments of the PRE were 56.0 and 368.2 ng cm-2, respectively, and the total burden of PBDEs in the PRE were estimated at 8.6 metric tons. The current ∑PBDEs and BDE 209 fluxes to the PRE were 2.1 and 29.7 ng cm-2 yr-1, respectively. The concurrent increase of BDE 209 fluxes and the annual gross industrial output values of electronics manufacturing revealed that the rapid growth of electronics manufacturing in this region since the early 1990s was responsible for the sharp rise of BDE 209 fluxes in the past decade. The PBDE congener compositions of the cores indicated the various input pathways for PBDEs transport to different locations of the estuary. [ABSTRACT FROM AUTHOR]

Surface sediment (0-5 cm) samples were collected from the Pearl River Estuary (PRE) and the adjacent northern South China Sea (SCS) in July 2002 and analyzed for 25 polycyclic aromatic hydrocarbons (PAHs) and 8 organochlorine pesticides (OCPs) including dichlorodiphenyl-trichloroethanes (DDTs), hexachlorocyclohexanes (HCHs), and heptachlor. The total PAHs and OCPs concentrations were 138-1100 and 0.18-3.57 ng/g dry weight, respectively. Compositional pattern analysis suggested that PAHs in the PRE were derived from both pyrogenic and petrogenic sources, whereas most PAHs in the northern SCS were pyrogenically originated. The concentrations of both PAHs and OCPs were higher in the PRE than in the northern SCS, and a decreasing trend with the distance from the estuary to the open sea was observed. In addition, perylene was a predominant component in all samples and clustered with PAH compounds with high log Kow values (from phenanthrene). These findings indicated that river outflows were the major source of contamination in the offshore sediments. A preliminary assessment suggested that atmospheric deposition contributed only a minor portion of PAHs or OCPs in the sediments of the northern SCS. The sediment (0-5 cm) mass inventories were 126 and 423 metric tons for PANs and were 0.4 and 1.4 metric tons for OCPs in the PRE and the northern SCS, respectively. Clearly, contaminated sediments of the northern SCS may be a potential source of PAHs and OCPs to the global oceans. [ABSTRACT FROM AUTHOR]

Riverine runoff is an important mode to transport anthropogenic pollutants from terrestrial sources to oceans. Polybrominated diphenyl ethers (PBDEs) were measured in riverine runoff samples from the eight major outlets within the Pearl River Delta (PRD), China, an economically fast developing region housing a vast number of electronics manufacturing and assembling plants. The Σ17-PBDEs (sum of 17 BDE congeners, i.e., BDE-28, -47, -66, -85, -99, -100, -138, -153, -154, -183, -196, -197, -203, -206, -207, -208, and -209) concentrations varied from 344 to 68000 pg/L, with those of BDE-209, BDE-47, and BDE-99 being 335- 65 200, 3-143, and <1-200 pg/L, respectively. These levels were in the high end of the global PBDEs concentrations in the aquatic environments. The monthly inputs of Σ17-PBDEs ranged from 0.21 to 215 kg at individual outlets, and the annual input of Σ17PBDEs from all the outlets was estimated at 2140 kg/year. Of the target BDE congeners, BDE-209 was the most predominant component with an annual input of 1960 kg/year, followed by BDE-47 (13.3 kg/ year) and BDE-99 (11.7 kg/year). An extrapolation of the past use of PBDEs in the region concluded that 23 metric tons of Σ17have been discharged into the coastal ocean from the PRD in the last 20 years. The amount of PBDEs imported to China in the form of e-waste was estimated at 35 000 metric tons/year, higher than the annual domestic production of brominated fire retardants (~10 000 metric tons/year) and the annual riverine input of total PBDEs from the PRD, suggesting that the majority of PBDEs inventory has been accumulated from importation of e-wastes. Because of the continuous importation of e-wastes and strong demand for brominated fire retardants, the impact of PBDEs on China's and the world's environments is expected to persist for many years to come. [ABSTRACT FROM AUTHOR]