Short- and medium-chain chlorinated paraffins in urban road dust of Shanghai, China: concentrations, source apportionment and human exposure assessment.

Chlorinated paraffins (CPs) are ubiquitous anthropogenic contaminants that have been found in various environmental media. The objective of this study was to determine concentrations, spatial distribution, possible sources and potential health risk of SCCPs and MCCPs in urban road dust collected from Shanghai, China. The concentrations ranged from 9.74 to 11,400 ng g-1 for ΣSCCPs, 44.1 to 49,900 ng g-1 for ΣMCCPs and 53.9 to 61,400 ng g-1 for total CPs, respectively. MCCPs were the dominant component in all road dust, averagely accounting for 82.8% of total CPs. The concentrations of CPs in dust collected from traffic and commercial areas were significantly higher than those from campus, industrial, park and residential areas (p < 0.01), which could be attributed to tire wear in heavy traffic. All dust samples were divided into two groups by hierarchical cluster analysis for both SCCPs and MCCPs, and the most abundant homologue groups in most samples were C10Cl7-10 and C13Cl7-9 for SCCPs, and C14Cl7-9 and C15Cl8-9 for MCCPs. Correlation analysis showed that all carbon homologues in road dusts were highly correlated each other, suggesting SCCPs and MCCPs in dust maybe came from similar sources. Three sources for CPs in dust samples were apportioned by the PMF model; their relative contributions to the total CPs burden in dust were 25.6% for factor 1 (commercial CP mixture), 13.7% for factor 2 (long-distance transport) and 60.7% for factor 3 (commercial CP mixture). The median estimated daily intakes of total CPs via road dust were 1.78 × 10-5 for children and 3.0 × 10-6 mg kg-1 day-1 for adults, respectively. Quantitative risk assessment using non-cancer hazard index and total margin of exposure of total CPs indicated that total CPs at the present level in road dust pose no significant risk for both children and adults in Shanghai.

Occurrence, source apportionment, and carcinogenic risk assessment of polycyclic aromatic hydrocarbons in urban road dusts in Shanghai.

Polycyclic aromatic hydrocarbons (PAHs), as a class of important environmental pollutants, have received considerable concern due to their widespread existence and biological toxicity. The main purpose of this study was to determine concentrations, spatial distribution, possible sources, and potential health risk of PAHs in urban road dust in Shanghai, China. The concentration of Σ26PAHs ranged from 53.0 to 28,700 ng g-1 in road dust samples from Shanghai, which is at the low to medium level compared with other areas around the world. PAHs with 4-5 rings were predominant components in road dust. The level of PAHs in road dust was significantly higher than those in soil and river sediment in Shanghai. Six possible sources of PAHs were apportioned by PMF model. The contribution of pyrogenic PAHs accounted for 91.3% of the total PAHs in road dusts. The motor vehicular emission, natural gas, and coal combustion were main sources for urban road dust PAHs from Shanghai. Four dibenzopyrene (DBP) isomers were contributed averagely 75% of total TEQBaP concentration. DBalP, BaP, DBaiP, BbF, and DBA were main contributors to total carcinogenic potency, which totally contributed from 69.6 to 91.8% (median 89.1%) to total TEQBaP in urban road dusts of Shanghai. The results of incremental lifetime carcinogenic risk (ILCR) assessment showed that the total risk values exposed to 24 PAHs in road dust were lower than 10-4 at all sampling sites, indicating that exposure to dust-bound PAHs at present level was unlikely to result in high carcinogenic risk for both children and adults in Shanghai.

Biomonitoring of polycyclic aromatic hydrocarbons and synthetic musk compounds with Masson pine (Pinus massoniana L.) needles in Shanghai, China.

Twenty-six polycyclic aromatic hydrocarbons (PAHs) and four synthetic musk compounds (SMCs) accumulated by Masson pine needles from different areas of Shanghai were investigated in the present study. Concentrations of Σ26PAHs (sum of 26 PAHs) ranged from 234 × 10-3 to 5370 × 10-3 mg kg-1. Levels of Σ26PAHs in different sampling areas followed the order: urban areas (Puxi and Pudong) > suburbs > Chongming. Total concentrations of 16 USEPA priority PAHs ranged from 225 × 10-3 to 5180 × 10-3 mg kg-1, ranking at a relatively high level compared to other regions around the world. Factor analysis and multi-linear regression model has identified six sources of PAHs with relative contributions of 15.1% for F1 (vehicle emissions), 47.8% for F2 (natural gas and biomass combustion), 7.8% for F3 (oil), 10.6% for F4 (coal combustion), 15.7% for F5 ("anthracene" source) and 3.0% for F6 (coke tar). Total concentrations of 4 SMCs varied between 0.071 × 10-3 and 2.72 × 10-3 mg kg-1 in pine needles from Shanghai. SMCs with the highest detected frequency were Galaxolide and musk xylene, followed by musk ketone and Tonalide. The highest level of SMCs was found near industrial park and daily chemical plant. The results obtained from this study may have important reference value for local government in the control of atmospheric organic pollution.

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.

Atmospheric occurrence, homologue patterns and source apportionment of short- and medium-chain chlorinated paraffins in Shanghai, China: Biomonitoring with Masson pine (Pinus massoniana L.) needles.

A comprehensive survey was conducted to Masson pine (Pinus massoniana L.) needles widely distributed in Shanghai in order to investigate the levels and homologue group patterns of short- and medium-chain chlorinated paraffins (SCCPs and MCCPs), to identify and quantitatively assess source contributions to the total CPs in pine needle samples. The concentration ranged from not detected (ND) to 13,600ngg(-1) with a geometric mean (GM) value of 63.7ngg(-1) for ΣSCCPs, from 12.4 to 33,500ngg(-1) with a GM value of 677ngg(-1) for ΣMCCPs, and from 14.0 to 45,700ngg(-1) with a GM value of 768ngg(-1) for total CPs. For different sampling units, the pollution levels both for SCCPs and MCCPs in pine needles were in the same orders: Pudong>suburbs>Puxi>Chongming. These significant differences in SCCPs and MCCPs among four sampling units could be associated with difference in industrial activities and to some extent also in population density. All pine needle samples (n=131) were divided into 2 groups by hierarchical cluster analysis (HCA) for SCCPs and MCCPs, the most abundant homologue groups in the bulk of pine needle samples were C11Cl5-7 and C13Cl5-7 for SCCPs, and C14Cl7-8 and C15Cl7-8 for MCCPs. Correlation analysis suggested that SCCPs and MCCPs in pine needles in the studied area may be derived from different sources. Four sources for pine needles were identified by the FA-MLR model; their relative contributions to the total CP burden in pine needles were 18.0% for F1 (attributed to commercial SCCP mixture), 42.2% for F2 (attributed to commercial MCCP mixture), 29.3% for F3 (attributed to LRAT), and 10.5% for F4 (unknown source). CP contamination of atmospheric air by point sources and long-range atmospheric transport in Shanghai should receive more attention by local government.

Occurrence, profiles, and ecological risks of polybrominated diphenyl ethers (PBDEs) in river sediments of Shanghai, China.

Fifty-two PBDE congeners in river sediments from Shanghai were analyzed in the present study. The concentrations of Σ51PBDEs (defined as the sum of 51 BDE congeners except BDE209) and BDE209 ranged from 0.231 to 119 ng g(-1) and from nd to 189 ng g(-1), respectively. The most abundant BDE congeners in surface sediments were BDE118, 207, 208, 99, 49, 75, 47, 71 and 209, with median values of 1.67, 1.81, 1.83, 1.87, 1.98, 2.52, 2.73, 4.62 and 45.7 ng g(-1) dw, respectively. The concentrations of Σ52PBDEs were significantly correlated with total organic carbon (TOC) content in sediments (p < 0.05). Weak correlations between all PBDE homologues and TOC (r < 0.32) suggest that TOC had a little influence on sediment PBDE transport and distribution patterns in river sediments of Shanghai. Correspondence analysis (CA) showed that PBDEs in sediments in the studied area originated from commercial BDE formulations, combustion emission sources, and debromination of highly brominated PBDEs by aerobic/anaerobic microbes or sunlight. Risk assessment based on risk quotients (RQ) showed that PBDEs in all river sediments collected from Shanghai posed a high potential ecological risk (RQ > 1) to the sediment dwelling organisms, and pentaBDE, decaBDE and tetraBDE were the major ecological risk drivers.

Occurrence, sources and health risk assessment of polycyclic aromatic hydrocarbons in urban (Pudong) and suburban soils from Shanghai in China.

A comprehensive investigation was conducted to the urban (Pudong) and suburban soils in Shanghai. A total of 154 soil samples were analyzed for 26 PAHs including highly carcinogenic dibenzopyrenes (DBPs). The total concentrations ranged from 25.8 to 7380 µg kg(-1) for Σ26PAHs and 18.8 to 6320 µg kg(-1) for 16 USEPA priority PAHs (Σ16PAHs), respectively. The BaP toxic equivalent (BaPeq) concentrations were between 6.41 and 2880 µg kg(-1) for Σ24PAHs, 1.11 and 620 µg kg(-1) for Σ16PAHs and 2.72 and 2250 µg kg(-1) for Σ4DBPs. The high PAH contamination in green land soils might originate mainly from local road traffic and industrial activities, and sewage sludge application or waste water irrigation for soil. Seven sources of soil PAHs in Shanghai were identified by positive matrix factorization (PMF) model. The mean risk quotient (m-RQ) values indicated that there were medium to high ecological risks in 9.10% of soil samples, pyrene (Pyr), benzo[b]fluoranthene (BbF) and benz[a]anthracene (BaA) were the major ecological risk drivers under agricultural use. The cancer risk (CR) values were within the acceptable range at 35.7%, 35.1% and 31.2% of sampling sites for children, youths and adults, respectively. The total lifetime carcinogenic risk (TLCR) values at 57.8% of sampling sites were within the acceptable range. Overall, cancer risks of soil PAHs in all sampling sites in the studied area were below the highest acceptable risk, suggesting that soil PAHs are unlikely to pose a significant cancer risk for population based on ingestion, dermal contact and inhalation exposure pathways.

Short- and medium-chain chlorinated paraffins in urban soils of Shanghai: spatial distribution, homologue group patterns and ecological risk assessment.

Chlorinated paraffins (CPs) are toxic, bioaccumulative, persistent, and ubiquitously present in the environment. Data on the presence of short- and medium-chain chlorinated paraffins (SCCPs and MCCPs) in urban areas with dense population are still scarce to date. SCCPs and MCCPs were measured in urban soils from Shanghai to comprehensively investigate their levels, spatial distribution, homologue group patterns and ecological risk. The concentrations of CPs in soils varied from ND to 615 ng g(-1) with a median value of 15.7 ng g(-1) for SCCPs and from 1.95 to 188 ng g(-1) with a median value of 7.98 ng g(-1) for MCCPs, respectively. The concentrations of SCCPs in most soils were higher than those of MCCPs. The total CP concentrations in soil samples were between 4.10 and 625 ng g(-1) with a median value of 26.4 ng g(-1). For different functional zones, the median concentrations of soil CPs were found higher in green land including park, greenbelt and campus than those in roadside. The highest concentrations of CPs in soils could be derived from sewage sludge application and wastewater irrigation for green land. Three types of soils were classified by hierarchical cluster analysis (HCA) for SCCPs and MCCPs, the most abundant homologue groups in the bulk of the soil samples were C11Cl5-7 and C13Cl5-7 for SCCPs, and C14Cl7-8 and C15Cl7-8 for MCCPs. Correlation analysis and PCA suggested that SCCPs and MCCPs in soils in the studied area derived from different sources. The preliminary ecological risk assessment indicates that soil CPs at present levels poses no significant ecological risk for soil-dwelling organisms.

Polycyclic aromatic hydrocarbons (PAHs) in urban soils of the megacity Shanghai: occurrence, source apportionment and potential human health risk.

A comprehensive investigation was conducted to the urban soil in the megacity Shanghai in order to assess the levels of PAHs and potential risks to human health, to identify and quantitatively assess source contributions to the soil PAHs. A total of 57 soil samples collected in main urban areas of Shanghai, China were analyzed for 26 PAHs including highly carcinogenic dibenzopyrene isomers. The total concentrations ranged from 133 to 8,650 ng g for ΣPAHs and 83.3 to 7,220 ng g for ΣPAHs, with mean values of 2420 and 1,970 ng g, respectively. DBalP and DBaeP may serve as markers for diesel vehicle emission, while DBahP is a probable marker of coke tar as distinct from diesel emissions. Six sources in Shanghai urban area were identified by PMF model; their relative contributions to the total soil PAH burden were 6% for petrogenic sources, 21% for coal combustion, 13% for biomass burning, 16% for creosote, 23% for coke tar related sources and 21% for vehicular emissions, respectively. The benzo[a]pyrene equivalent (BaP) concentrations ranged from 48.9-2,580 ng g for ΣPAHs, 7.02-869 ng g for ΣPAHs and 35.7-1,990 ng g for ΣDBPs. The BaP concentrations of ΣDBPs made up 72% of ΣPAHs. Nearly half of the soil samples showed concentrations above the safe BaP value of 600 ng g. Exposure to these soils through direct contact probably poses a significant risk to human health from carcinogenic effects of soil PAHs. The index of additive cancer risk (IACR) values in almost one third of urban soil samples were more than the safe value of 1.0, indicating these urban soil PAHs in the study area may pose a potential threat to potable groundwater water quality from leaching of carcinogenic PAH mixtures from soil.

Short-chain chlorinated paraffins (SCCPs) in surface soil from a background area in China: occurrence, distribution, and congener profiles.

Short-chain chlorinated paraffins (SCCPs) are extremely complex technical mixtures of polychlorinated n-alkanes with carbon chain lengths from C10 to C13 and chlorine content between 49 and 70%. SCCPs are under consideration for inclusion in the Stockholm Convention on persistent organic pollutants. SCCPs have been used extensively in industrial production, but little is known about the pollution level in soil environment in China. In this study, levels and distribution of SCCPs in soil samples from Chongming Island were analyzed. Concentrations of total SCCPs in soil samples ranged from 0.42 to 420 ng g(-1), with a median of 9.6 ng g(-1). The ubiquitous occurrence of SCCPs in Chongming Island implied that long-range atmospheric transport and soil-air exchange may be the most important pathways for SCCP contamination in the background area. The localized SCCP contamination could be derived from an unidentified source. Hierarchical cluster analysis indicated that C13- and C11-congeners were predominant in most soils and C10- and C12-congeners dominated in the remaining soils. Cl7- and Cl8-congeners were on the average the most dominant chlorine congeners in nearly all soils. Principal component analysis suggested that the separation of even and odd carbon chain congeners occurred during long-range atmospheric transport and aging in soil in the study area.

[Level, composition and sources of medium-chain chlorinated paraffins in soils from Chongming Island].

In order to understand the contents, spatial distribution and sources of medium-chain chlorinated paraffins (MCCPs) in the soils from Chongming Island, the concentrations of MCCPs in 27 soil samples were analyzed by GC-ECNI-MS. The total concentrations of MCCP8 (sigma MCCPs) in all samples ranged from 2.56-96.3 ng x g(-1), with a median of 7.32 ng x g(-1). All soil samples were classified into two categories by cluster analysis. C14-MCCPs and C15-MCCPs, and Cl5-MCCPs and Cl6-MCCPs were the most predominant carbon and chlorine congener groups in most of the samples, accounting for 29.8% and 28.9%, and 29.9% and 23.3%, respectively. C14-MCCPs were the most predominant carbon congener groups in some samples, accounting for 68.5%, which was similar to that of CP-52. Atmospheric deposition and soil-air exchange were the major sources of MCCPs for soils in Chongming. Soils at a few sites were probably contaminated by sewage sludge from sewage treatment plants (STPs) or other unidentified source. No significant correlations were observed between MCCPs and TOC. The correlation analysis also showed significant correlation among the carbon congener groups of MCCPs, which suggested that MCCP congener groups might have been derived from similar sources. Compared to other studies at home and abraod, the MCCPs concentrations in the present study were at a lower level.

[Levels, distribution and possible sources of polychlorinated biphenyls in river sediments from an electronic waste recycling area].

The concentrations of 144 polychlorinated biphenyls (PCBs) in the river sediments from Luqiao were analyzed by GC-muECD. The objectives of this study were to understand the contents, spatial distribution and possible sources of PCBs. The Sigma PCBs concentrations detected in the river sediments were in the range of 1.66 to 5 930 ng x g(-1), with a mean of 763 ng x g(-1). Tri-CBs, tetra-CBs and penta-CBs were the primary PCB congeners in all samples, accounting for 2.63%-57.6%, 10.4%-54.6% and 7.82%-46.1%, respectively. Octa-CBs and deca-CBs were the minor PCB congeners in all samples, with the percentages of 0-8.57% and 0-11.0%, respectively. The hierarchical cluster analysis (HCA) showed that 22 samples were mainly polluted by Ar1248, 9 samples were polluted by Ar1254, and 6 samples were contaminated by Ar1016, Ar1232 and Ar1242. The PCBs concentrations found in the present study were at an upper-middle level compared with those in other studies in the world. The PCBs pollution in the present area had a high ecological risk.

Internal carotid artery in the operative plane of endoscopic endonasal transsphenoidal surgery.

The objective of this study was to measure the related parameters of intercarotid artery (ICA) in the operative plane of endonasal transsphenoidal approach for hypophyseal surgeries. Nine parameters of the ICA were examined in the computed tomographic angiographic (CTA) scan of 101 patients. The shortest distance between the middle point of the nasal columella and the projective point of the ICA (D(3)) was 85.50 (5.79) mm. The shortest distance between the anterior wall of the sphenoid sinus and the projective point of the ICA (D(4)) was 16.93 (3.50) mm. The distance between the bilateral projective points of the ICA (D(5)) was 21.60 (3.45) mm. The shortest distance from the anterior wall of the sphenoid sinus to the line between the bilateral projective points of the ICA (D(6)) was 12.1 (3.91) mm. The shortest distance between the middle point of nasal columella and the anterior wall of the sphenoid sinus (D(7)) was 72.67 (5.99) mm. The width of the angle between the bilateral ICA projective point from the middle point of the nasal columella (A(1)) was 14.9 (2.32) degrees. The width of the angle between the bilateral ICA projective points from the anterior-most point of sphenoid sinus (A(2)) was 85.49 (18.12) degrees. Clinically, it is relatively safe to work within the distances and angles measured in this research, and these results may provide information for clinical surgery of pituitary tumor.

[Characteristics of polychlorinated biphenyls in soils from an electronic waste recycling area].

The concentrations of 144 polychlorinated biphenyls (PCBs) in the soils from Luqiao were analyzed by GC-microECD. The objectives of this study were to understand the contents, spatial distribution and sources. The sigma PCBs concentrations in soils samples were in the range of 0.779 ng x g(-1) to 937 ng x g(-1), with a mean of 75.7 ng x g(-1), and the relatively high level of PCBs were mainly distributed in the south central area. Penta-CBs, hexa-CBs and tetra-CBs were the primary homologues in 38 samples, with the range of 13.0% - 61.1%, 4.59% - 48.8% and 10.1% - 31.5%, respectively. Di-CBs was the most predominant homologues in other samples, with the range of 47.1% - 75.2%. The hierarchical cluster analysis (HCA) showed that most of samples were mainly polluted by Ar1254, few samples were polluted by Ar1221. Significant correlations were observed between sigma PCBs and TOC, which suggested PCBs were affected by TOC in soils. The correlation analysis also showed significant correlation among the PCBs homologues (except di-CBs and nona-CBs), which suggested PCBs might have the similar sources. Compared to other studies from different countries and regions, the PCBs concentrations in the present study were at an upper-middle level.

[Level, distribution, and source identification of polychlorinated naphthalenes in surface agricultural soils from an electronic waste recycling area].

The concentration of 46 polychlorinated naphthalenes (PCNs) in the agricultural soils from Luqiao was analyzed by GC-NCI-MS. The objectives of this study were to investigate the contents, spatial distribution and sources of PCNs. The total concentrations of PCNs (sigma PCNs) in soil samples were in the range of 0.062 to 2.92 ng x g(-1), with a mean of 0.630 ng x g(-1). Tetra-CNs and penta-CNs were the predominant homologues in most of the samples, accounting for 18.4% - 88.8% and 8.40% - 53.1%, with average values of 46.7% and 30.7%, respectively, followed by tri-CNs, accounting for 0 - 47.3%, with a mean of 10.6%. Cluster analysis and combustion marker analysis showed that the sampling sites were mainly polluted by Halowax 1014 and Halowax 1013, also possibly polluted by PCBs mixtures and e-waste combustion process. Compared to other studies, the PCNs concentration in this study was at a medium level.

[Levels, distribution and possible sources of polybrominated diphenyl ethers in river sediments from an electronic waste recycling area].

The concentrations of 41 polybrominated diphenyl ethers (PBDEs) in the river sediments from Luqiao were analyzed by GC-NCI-MS. The objectives of this study were to understand the contents, spatial distribution and sources. The Sigma40 PBDEs (excluding BDE209) concentrations in sediments sampled were in the range of 0.177 to 161 ng x g(-1), with a mean of 22.5 ng x g(-1), and the concentrations of BDE209 were from 0.36 to 958 ng x g(-1), with a mean of 148 ng x g(-1). Deca-BDE was the most predominant in 9 PBDE homologues in most of samples, accounting for 38.4%-96.0%, with an average of 74.4% nona-BDEs and hepta-BDEs, accounting for 3.3%-25.8% and 0.01%-14.1%, respectively. Significant correlations were observed among all of PBDEs congeners, which suggested these PBDEs might have the similar sources. The homologue composition of PBDEs and hierarchical cluster analysis (HCA) showed that most of sampling sites were mainly polluted by deca-BDE formulation, and others polluted by deca-BDE and octa-BDE formulations. Compared to other studies from different countries and regions, the PBDEs concentrations in the present study were at a medium-to-low level. But it should be concerned that a few of sampling sites were highly contaminated by point sources.

[Residues of organochlorine pesticides in urban soil of Shanghai].

The 55 soil samples were collected from Shanghai urban areas in March 2007. The residues and distribution characteristics of organochlorine pesticides (OCPs) in the soil samples were investigated with gas chromatography. The results showed that HCHs, DDTs, and HCB were in the ranges of nd-38.58 microg x kg(-1), 1.81-79.61 microg x kg(-1) and 0.16-40.25 microg x kg(-1), respectively. The total OCPs concentrations in urban soil of Shanghai ranged from 3.12 microg x kg(-1) to 91.07 microg x kg(-1) with a mean of 22.33 microg x kg(-1), and the p,p'-DDE took over 60% of the total OCPs. The main contaminated areas were distributed in the park and greenbelts. The composition of OCPs indicated that OCPs in soil samples mainly came from historical application. Compared to the reference data, the pollution burden in soil of Shanghai was lower than those in other areas of China and in German, Argentina and Poland.