Pine needles as biomonitors of polybrominated diphenyl ethers and emerging flame retardants in the atmosphere of Shanghai, China: occurrence, spatial distributions, and possible sources.

In this study, pine needles were used as biomonitors to investigate the levels, spatial distributions, and possible sources of polybrominated diphenyl ethers (PBDEs) and four emerging halogenated flame retardants (HFRs) in the atmosphere of Shanghai, China. The four emerging HFRs were hexabromocyclododecane (HBCD), decabromodiphenylethane (DBDPE), 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE), and dechlorane plus (DP), with the first 3 HFRs being non-polybrominated diphenyl ether brominated flame retardants (non-PBDE BFRs). The total concentrations ranged from 3.71 to 4020 ng g-1 dry weight (dw) for 52 PBDE congeners (Σ52BDEs), < MDL (method detection limit) to 15.2 ng g-1 dw for three non-PBDE BFRs (Σ3non-PBDE BFRs), and 0.815 to 1090 pg g-1 dw for two DP isomers (ΣDP), respectively. High levels of PBDEs, three non-PBDE BFRs, and DP were found in pine needles from suburbs and Pudong, which was a consequence of industrial activities. The fraction of anti-DP isomer (fanti) in pine needles ranged from 0.515 to 0.939 with a mean value of 0.721, and most of the fanti values were consistent with those of technical DP formulations. Principal component analysis-multiple linear regression (PCA-MLR) model identified four sources of PBDEs in pine needles with the quantified contributions: degradation of technical PBDE formulations (49.5%), technical deca-BDE (6.9%), technical penta-BDE (25.1%), and technical octa-BDE (18.5%). These findings are expected to help understand the pollution level, fate, and possible sources of HFRs in the atmosphere of Shanghai and provide a basis for air pollution control and management in Shanghai.

Occurrence, sources, partitioning and ecological risk of short- and medium-chain chlorinated paraffins in river water and sediments in Shanghai.

The characteristics of regional environmental pollution of short- and medium-chain chlorinated paraffins (SCCPs and MCCPs) in river system from Shanghai were comprehensively investigated in this study for the first time. The total concentrations of SCCPs and MCCPs ranged from 15.0 to 1640 ng L-1 (median: 278 ng L-1) and 40.3 to 3870 ng L-1 (median: 939 ng L-1) in water, and from not detected (ND) to 2020 ng g-1 (median: 89.3 ng g-1) and 10.1 to 10,800 ng g-1 (median: 947 ng g-1) in sediments, respectively. The higher levels of SCCPs and MCCPs were found in water from Jinhui and Yexie rivers, and in sediments from Huangpu River, respectively. The concentrations of MCCPs were higher than those of SCCPs in both water and sediments, suggesting that the river system was mainly contaminated by MCCPs. Compared with other areas around the world, the concentrations of SCCPs and MCCPs were at medium to high levels in water and sediments. Factor analysis results revealed that SCCPs and MCCPs had different sources in both water and sediments. The log Koc values of CPs were significantly correlated with carbon chain lengths (p < 0.01), but not with chlorine number for both SCCPs and MCCPs (p > 0.05). A significant second-order polynomial relationship was observed between log Koc values and molecular weights of homologue groups of SCCPs (p < 0.001) and MCCPs (p < 0.01), respectively. SCCPs in water posed a low ecological risk at all sampling sites, and MCCPs in water posed a moderate ecological risk to aquatic life at nearly a fifth of sampling sites. SCCPs and MCCPs in sediments posed a low ecological risk to sediment dwelling organisms at most sampling sites.

Spatial variations, source apportionment and potential ecological risks of polycyclic aromatic hydrocarbons and synthetic musks in river sediments in Shanghai, China.

The aims of this study were to investigate the levels, possible sources and potential ecological risks of 26 polycyclic aromatic hydrocarbons (PAHs) including highly carcinogenic dibenzopyrene (DBP) isomers and 4 synthetic musks (SMs) in river sediments from Shanghai. 74 sediment samples were collected from the Huangpu River and its main tributaries. The total concentrations ranged from 52.0 to 11400 ng g-1 for Σ26PAHs, 25.1-9910 ng g-1 for 16 USEPA priority PAHs (Σ16PAHs), 0.769-384 ng g-1 for Σ4DBPs, and 0.080-63.3 ng g-1 for Σ4SMs, respectively. Seven sources of PAHs in river sediments were identified by positive matrix factorization (PMF) model. Coal combustion, vehicle and creosote were the major emission sources for PAHs. SMs came mainly from domestic and industrial wastewaters. The toxic equivalent quantities of the benzo[a]pyrene (TEQBaP) ranged from 7.64 to 3920 ng g-1 for Σ24PAHs, 2.07-1150 ng g-1 for Σ16PAHs, and 5.53-3150 ng g-1 for Σ4DBPs. The TEQBaP of Σ4DBPs made up 73.9% of Σ24PAHs, which indicated that DBPs were the major carcinogenic contributors to total PAHs in sediments. According to sediment quality guidelines (SQGs) and mean PEL-Q values, the risks posed by PAHs in sediments were at medium level at most sampling sites, and SMs posed a low ecological risk to sediment-dwelling organisms in Shanghai.

Occurrence, homologue patterns and source apportionment of short- and medium-chain chlorinated paraffins in suburban soils of Shanghai, China.

In order to systematically investigate the spatial distribution, homologue profiles, and sources of short- and medium-chain chlorinated paraffins (SCCPs and MCCPs) in suburban soils in Shanghai, SCCPs and MCCPs in soils were analyzed using gas chromatography coupled with low resolution mass spectrometry in electron capture negative ion (ECNI) mode (GC-ECNI-MS). The CP concentrations in soils were between not detected (ND) - 697 ng g-1 with a median value of 3.52 ng g-1 for SCCPs, and ND - 666 ng g-1 with a median value of 15.3 ng g-1 for MCCPs, respectively. The concentrations of MCCPs in most soils were higher than that of SCCPs. The total CP concentrations (sum of SCCPs and MCCPs) in soils varied from ND to 964 ng g-1 with a median value of 20.5 ng g-1. The concentration of MCCPs was higher than that of SCCPs in most soils. The levels of SCCPs and MCCPs in suburban soils in Shanghai were at the medium level when compared to other areas around the world. No significant correlation was observed between soil CP concentrations and total organic carbon contents (p > 0.05). For different use type of soils, the median concentrations of CPs in soils were found higher in greenland than that in other areas probably due to busy traffic, sewage sludge application and/or wastewater irrigation. All soils were divided into two groups by hierarchical cluster analysis (HCA) both for SCCPs and MCCPs. Three discharge sources of CPs in suburban soil of Shanghai were identified by PMF model.