Runxia Sun

Distribution of organophosphorus flame retardants in sediments from the Pearl River Delta in South China.

Twelve organophosphorus flame retardants (PFRs) were identified in the sediments and the sediment core collected from the rivers and the estuary in the Pearl River Delta, with the aim of investigating their spatial and vertical distributions. The concentrations of PFRs ranged from 8.3 to 470 ng/g dry weight with high levels of PFRs in the urban area and the e-waste recycling region. Generally, TPhP, TCPP, TEHP, TCEP, and TBEP were the dominant compounds of the PFRs, the composition of which varied across the different regions, reflecting the different sources of PFRs. In the estuary, the PFRs mainly derived from the Xijiang River and the Shunde sections. Increased concentrations of halogen-containing PFRs have been observed in the upper layers of the sediment core. Conversely, relatively high concentrations of halogen-free PFRs were observed in the lower layers of the sediment core, indicating different usage patterns or environmental behaviors between the halogen and the non-halogen PFRs in the study area.

An eight year (2005–2013) temporal trend of halogenated organic pollutants in fish from the Pearl River Estuary, South China

Dichlorodiphenyltrichloroethane and its metabolites (DDTs), hexachlorocyclohexanes (HCHs), polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), dechlorane plus (DP), 2,3,5,6-tetrabromo-p-xylene (pTBX) and pentabromotoluene (PBT) were measured in baby croaker (Collichthys lucidus) and mullet (Osteomugil ophuyseni) collected in 2005 and 2013 from the Pearl River Estuary. DDTs, HCHs, PCBs, and PBDEs were detected in two fish species at concentrations of 150-8100, 1.4-120, 22-560, 2.2-280 ng/g lipid wt., respectively. The levels of these chemicals were significantly lower in 2013 than in 2005. The compositions for DDTs, HCHs, and PBDEs in 2013 differed from those in 2005, indicating source changes between the two sampling periods. DP, pTBX and PBT were detected at concentrations of ND-130 ng/g lipid wt. No clear temporal trends were found for these contaminants. Overall, these results indicated the effectiveness of regulations and source controls in substantively reducing inputs of these contaminants to the Pearl River Estuary.

Polycyclic aromatic hydrocarbons in surface sediments and marine organisms from the Daya Bay, South China.

Polycyclic aromatic hydrocarbons (PAHs) were investigated in the marine ecosystem of the Daya Bay, South China. The PAH concentrations ranged from 340 to 710 ng/g dry weight in the sediments and from 110 to 520 ng/g wet weight in marine organisms, respectively. The dominant compounds were three- and four-ring PAHs in the sediments (53%-89%) and two- and three-ring PAHs in the marine species (67%-94%), respectively. PAHs mainly originated from both pyrolytic and petrogenic sources. Comparison with the effects-based sediment quality guideline values suggested that the ecological risk caused by the total PAHs was relatively low (less than 25% incidence of adverse effects) in the sedimentary environment. The median cancer risk level via seafood consumption (1.6 × 10(-5) for urban residents and 1.2 × 10(-5) for rural residents, respectively) was slightly higher than the maximum admissible level (10(-5)) set by US EPA, but lower than the priority risk level (10(-4)).

Persistent halogenated compounds in fish from rivers in the Pearl River Delta, South China: Geographical pattern and implications for anthropogenic effects on the environment.

Three fish species, mud carp (Cirrhinus molitorella), tilapia (Tilapia nilotica), and plecostomus (Hypostomus plecostomus), from rivers in the Pearl River Delta (PRD) were analyzed for dichlorodiphenyltrichloroethane and its metabolites (DDTs), hexachlorocyclohexanes (HCHs), polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), decabromodiphenyl ethane (DBDPE), and Dechlorane Plus (DP). The concentrations of DDTs, HCHs, PCBs, PBDEs, DBDPE, and DP ranged from 380-57,000, 5.5-100, 30-4200, 6.9-690, 0.29-460, and 0.09-20ng/g lipid weight, respectively. Congener profiles or chemical compositions of PBDEs, DPs, DDTs, and HCHs in plecostomus differed significantly from those in the other two fish species, which can be ascribed to species-specific metabolism. DDTs derived from historical residue and land erosion remained the predominant pollutants in the PRD, while industrial and urban activities resulted in elevated levels of PCBs and PBDEs in the metropolitan area. E-waste recycling activities have greatly impacted on the adjacent aquatic environment, and the potential point source for DBDPE was also revealed.

Legacy and emerging halogenated organic pollutants in marine organisms from the Pearl River Estuary, South China

A suite of legacy and emerging halogenated organic pollutants (HOPs) were measured in marine organisms (coastal fish and invertebrates) from the Pearl River Estuary, South China, to investigate the current contamination status after the Stockholm Convention was implemented in China. Dichlorodiphenyltrichloroethane and its metabolites (DDTs), polychlorinated biphenyls (PCBs), and polybrominated diphenyl ethers (PBDEs) were detected in all samples at concentrations of 54-1500, 16-700, and 0.56-59ng/g lipid weight, respectively. Dechlorane Plus (DP), decabromodiphenyl ethane (DBDPE), 2,3,5,6-tetrabromo-p-xylene (pTBX), and pentabromotoluene (PBT) were also found at concentrations of ND (non-detectable) to 37ng/g lipid weight. The concentrations of these investigated contaminants in the present study were at moderate levels, as compared with those reported in other regions. Significant interspecies differences were found in the levels of DDTs, PCBs, PBDEs and the alternative halogenated flame retardants (AHFRs). DDTs were the predominant HOPs in those species and represented >50% of the total HOPs, followed by PCBs, PBDEs, and AHFRs. The total estimated daily intakes (EDIs) of DDTs, PCBs, PBDEs, and AHFRs were 28, 12, 1.0, and 0.18 (ng/kg)/d, respectively, via seafood consumption. These concentrations are not expected to pose health risks to humans.

Spatial–temporal trend and health implications of polycyclic aromatic hydrocarbons (PAHs) in resident oysters, South China Sea: A case study of Eastern Guangdong coast

Spatial and temporal distributions of polycyclic aromatic hydrocarbons (PAHs) were investigated in Eastern Guangdong coast, China. Total PAH concentrations in oysters ranged from 231 to 1178ng/g with a mean concentration of 622ng/g dry weight. Compared with other bays and estuaries, PAH levels in oysters were moderate. Spatial distribution of PAHs was site specific, with relatively high PAH concentrations observed in Zhelin Bay and Kaozhouyang Bay. Based on the Spearman test analysis, only PAH concentration in oysters from Jiazi Harbor showed a significant increasing trend (P<0.05). Three-ring PAHs were the most abundant, accounting for 54.2%-88.4% of total PAHs. Diagnostic ratios suggested that PAHs were derived mainly from petroleum origin. BaP and ∑4PAH concentrations were well within the European Union limits (5ng/g and 30ng/g wet weight, respectively). The incremental lifetime cancer risks (ILCR) for PAHs were <10(-5), indicating that the adverse health risks associated with oyster consumption in this area were minimal.

Short-chain chlorinated paraffins in marine organisms from the Pearl River Estuary in South China: Residue levels and interspecies differences.

There is limited information available on the bioaccumulation of short-chain chlorinated paraffins (SCCPs), a complicated group of persistent organic pollutants (POPs) candidates listed in the Stockholm Convention, in estuarine ecosystem. This study analyzed SCCPs in marine organisms (five fish and six invertebrates) from the Pearl River Estuary in South China. The concentrations of total SCCPs ranged from 210 to 21,000 ng · g(-1) lipid weight, with relatively higher levels in benthic invertebrates (shrimp, crabs and bivalves) than in non-benthic species (pelagic and mesopelagic fish and squid). SCCPs were biomagnified from prey fish (tapertail anchovy, Coilia mystus) to predator fish (Bombay duck, Harpadon nehereus), and the biomagnification factors (BMFs) of SCCP congeners ranged from 1.1 (C10H16Cl6) to 3.4 (C13H18Cl10). Species-specific homologue group patterns were also observed, with significantly lower proportions of C10 congeners in the shrimp, bivalves and Bombay duck than in the other species.

The distribution and accumulation of phosphate flame retardants (PFRs) in water environment

Phosphate flame retardants (PFRs) were measured in surface water (n=11), suspended particle matter (SPM, n=11), sediment (n=11), and fish samples (n=26) from the Pearl River Delta located in South China. Triethyl phosphate (TEP), tri(2-chloroethyl) phosphate (TCEP), tris(chloroisopropyl) phosphate (TCIPP), tri-n-butyl phosphate (TNBP), triphenyl phosphate (TPHP), and tricresyl phosphate (TMPP) were detected in more than half of surface water, SPM, and sediment samples. The median ΣPFR levels were 837ng/L, 54.6ng/g dry weight (dw), and 37.1ng/g dw in surface water, SPM, and sediment samples, respectively. No significant correlations were found between the concentrations of most PFRs and organic carbon contents in SPM and sediment (p>0.05). In surface water samples, tris(2-butoxyethyl) phosphate (TBOEP, 27% of ΣPFRs) and TEP (23% of ΣPFRs) were the predominant chemicals, while TNBP (38% of ΣPFRs) and TCEP (32% of ΣPFRs) dominated in ΣPFRs in SPM samples, and TCEP (48% of ΣPFRs) and TCIPP (25% of ΣPFRs) dominated in ΣPFRs in sediment samples. The proportions of phenyl-PFRs and chlorinated-PFRs in ΣPFRs increased from surface water to SPM and sediment. The distribution ratios of PFRs between water and organic carbon in SPM (or observed KOC) were generally 2-3 orders of magnitude higher than the predicted KOC. TNBP (nd-2.42ng/g wet weight (ww)), TCEP (nd-4.96ng/g ww), and TCIPP (nd-2.42ng/g ww) were detected in 27%, 35%, and 23% of all fish samples, respectively. The log bioaccumulation factors (BAFs) ranged 2.56-2.78, 2.15-3.11, and 2.61-3.10 for TNBP, TCEP, and TCIPP, respectively. The biota-sediment accumulation factors (BSAFs) of TNBP, TCEP, and TCIPP were generally lower than 1 except for the BSAF of TCIPP in common carp. The results indicate the species-specific bioaccumulation of PFRs in fish species.

Stereoselective bioaccumulation of syn- and anti-Dechlorane plus isomers in different tissues of common carp (Cyprinus carpio)

Common carps (Cyprinus carpio) were exposed to syn- and anti-Dechlorane Plus (DP) isomers to investigate absorption, tissue distribution, and stereoselective bioaccumulation of DP isomers. The absorption efficiencies of anti-DP in the gastrointestinal system were higher than those of syn-DP. A linear accumulation was found for both isomers in all fish tissues except for serum; and the liver and gill exhibited the highest and lowest DP assimilation efficiency, respectively. The elimination of DP isomers in all tissues followed first-order kinetics, with the fastest depuration rate occurring in the liver and serum. The biomagnification factors (BMFs) of both isomers were less than one in all tissues, except for serum. Anti-DP was preferably accumulated in the liver, gill, and serum, whereas syn-DP was selectively accumulated in the carcass and gastrointestinal tract. As a whole, fish did not show selective accumulation of the syn- or anti-DP isomer in the uptake stage, whereas a selective accumulation of syn-DP in fish was observed during the depuration period, which could be due to a selective excretion of anti-DP. Metabolism cannot be ruled out as a possible reason considering the high fanti values and the high elimination rate of DPs in the liver.

Hexabromocyclododecanes (HBCDs) in fish: Evidence of recent HBCD input into the coastal environment

Hexabromocyclododecanes (HBCDs) are flame retardants and emerging persistent organic pollutants. In the present study, α-, β-, and γ-HBCDs were measured in several fish species from rivers and an electronic waste (e-waste) recycling site in Pearl River Delta, South China. The concentrations of HBCDs were 12.8 to 640, 5.90 to 115, and 34.3 to 518ng/g lipid weight (lw) in mud carp (Cirrhinus molitorella), tilapia (Tilapia nilotica), and plecostomus (Hypostomus plecostomus), respectively. Plecostomus showed the highest HBCD concentrations among three fish species. The contributions of α-HBCD to total HBCDs were 78% to 97%, 93% to 99%, and 87% to 98% in carp, tilapia, and plecostomus, respectively. Fish samples from a harbor and the e-waste site exhibited the highest HBCD concentrations among all samples. The HBCD concentrations were not significantly correlated with the gross domestic product or population data. e-Waste recycling activities, harbor construction, and shipment might be recent HBCD sources.