Guoying Sheng

Chlorinated and polycyclic aromatic hydrocarbons in riverine and estuarine sediments from Pearl River Delta, China

Spatial distribution of chlorinated hydrocarbons [chlorinated pesticides (CPs) and polychlorinated biphenyls (PCBs)] and polycyclic aromatic hydrocarbons (PAHs) was measured in riverine and estuarine sediment samples from Pearl River Delta, China, collected in 1997. Concentrations of CPs of the riverine sediment samples range from 12 to 158 ng/g, dry weight, while those of PCBs range from 11 to 486 ng/g. The CPs concentrations of the estuarine sediment samples are in the range 6-1658 ng/g, while concentrations of PCBs are in the range 10-339 ng/g. Total PAH concentration ranges from 1168 to 21,329 ng/g in the riverine sediment samples, whereas the PAH concentration ranges from 323 to 14,812 ng/g in the sediment samples of the Estuary. Sediment samples of the Zhujiang River and Macao harbor around the Estuary show the highest concentrations of CPs, PCBs, and PAHs. Possible factors affecting the distribution patterns are also discussed based on the usage history of the chemicals, hydrologic condition, and land erosion due to urbanization processes. The composition of PAHs is investigated and used to assess petrogenic, combustion and naturally derived PAHs of the sediment samples of the Pearl River Delta. In addition, the concentrations of a number of organic compounds of the Pearl River Delta samples indicate that sediments of the Zhujiang river and Macao harbor are most likely to pose biological impairment.

Persistent organic pollutants in environment of the Pearl River Delta, China: an overview

In the Pearl River Delta of China, the rapidly developing industrial and agricultural activities, municipal development and use of chemicals caused serious environmental problems. This report summarizes the published scientific data on POPs in the environment of the Pearl River Delta, including the levels of POPs in the air, water, soil, river and estuarine sediments, the marine organisms like fish and shellfish in this region. The data preliminarily reveal the state of contamination in this region and give insight into the fate of POPs in this sub-tropical area. However, most research in this area is limited to a few kinds of POP compounds.

Levels, composition profiles and sources of polycyclic aromatic hydrocarbons in urban soil of Shanghai, China.

Levels, composition profiles and sources of polycyclic aromatic hydrocarbons (PAHs) were analyzed in 55 surface soil samples collected from Shanghai urban districts. The total concentrations of 22 PAHs (SigmaPAHs) ranged from 442 to 19,700 microgkg(-1), with a mean of 3780 microgkg(-1), and the sum of 16 priority PAHs (Sigma16PAHs) varied from 347 to 17,900 microgkg(-1), with a mean of 3290 microgkg(-1), and the seven possible carcinogenic PAHs (Sigma7CarPAHs) accounted for 36-58% of Sigma16PAHs. Among different functional areas, the higher level of PAHs was found in the roadside, followed by greenbelt, commercial district, park, and residential district. The composition of PAHs was characterized by the high molecular weight PAHs, among which fluoranthene, pyrene, benzo[b]fluoranthene and chrysene were most dominant components. A correlation analysis showed that there was relatively good correlation among the individual PAHs, but the contents of PAHs were poorly correlated with soil total organic carbon (TOC). A principal component analysis and PAHs isomeric ratios indicate that PAHs in Shanghai urban soil mainly originated from combustion. The toxic assessment suggested that soil PAHs exposure is medium carcinogenic at present level.

Pollution characterization and diurnal variation of PBDEs in the atmosphere of an E-waste dismantling region.

Diurnal air samples were collected from the E-waste dismantling region Guiyu and the underwear industry region Chendian. This was the first report to present the diurnal variation of PBDEs in the atmosphere. The average concentrations of 11 PBDE congeners were 11,742 pgm(-3) in the daytime, and 4830 pgm(-3) at night in Guiyu, while the concentrations were lower in Chendian with 376 pgm(-3) in the daytime, and 237 pgm(-3) at night. BDE-209 accounted for 22% and 31.3% of the total PBDEs in Guiyu and Chendian, respectively. The diurnal variation trends of BDE-47, -99, -153, -183, and -209 were also analyzed in detail in the two regions.

Urban roadside aromatic hydrocarbons in three cities of the Pearl River Delta, People's Republic of China

Urban roadside levels of benzene, toluene, ethylbenzene and xylenes (BTEX) were investigated in three typical cities (Guangzhou, Macau and Nanhai) in the Pearl River Delta Region of south China. Air samples were collected at typical ground level microenvironments by multi-bed adsorbent tubes. The BTEX concentrations were determined by thermal desorption–gas chromatography–mass selective detector (TD–GC–MSD) technique. The mean concentrations of benzene, toluene, ethylbenzene and xylenes were, respectively, 51.5, 77.3, 17.8 and 81.6mg/m 3 in Guangzhou, 34.9, 85.9, 24.1, 95.6mg/m 3 in Macau, and 20.0, 39.1, 3.0 and 14.2mg/m 3 in Nanhai. The relative concentration distribution pattern and mutual correlation analysis indicated that in Macau BTEX were predominantly traffic-related while in Guangzhou benzene had sources other than vehicle emission. In Nanhai, both benzene and toluene had different sources other than vehicle emission. The samples collected from Guangzhou showed that BTEX had significant higher concentrations in November than those in July. r 2002 Elsevier Science Ltd. All rights reserved.

Determination of Dechlorane Plus in Serum from Electronics Dismantling Workers in South China

Previous studies have reported high serum concentrations of polybrominated diphenyl ethers in residents of an electronic waste (e-waste) dismantling site in Guiyu town, South China. In this study, serum levels of Dechlorane Plus (DP), a chlorinated flame retardant of growing concern, were measured in residents of this region, and compared to those of a matched cohort from a nearby region in Haojiang, where fishing is the dominant industry. DP was detected in all the serum samples, with concentrations ranging from 7.8 to 465 ng/g lipid (median: 42.6 ng/g) and 0.93 to 50.5 ng/g lipid (median: 13.7 ng/g) in Guiyu and Haojiang, respectively. The Pearsons correlation coefficient between DP and decabromodiphenyl ether showed a positive relationship in Guiyu (r = 0.931, p < 0.01), but no correlation in Haojiang (r = 0.321, p = 0.34). The average anti-DP fractional abundances (f(anti) ratio) were 0.58 +/- 0.11 and 0.64 +/- 0.05 for Guiyu and Haojiang, respectively (p < 0.01). Tentatively identified dechlorination product ([-Cl + H]) was found in 19/40 serum samples (11/20 for Guiyu, 8/20 for Haojiang). These results suggest that the Guiyu and Haojiang cohorts experienced different dominant exposure routes. It is also possible that DP could bioaccumulate in a stereoselective manner, and undergo dechlorination metabolism. To the best of our knowledge, this is the first study to report DP levels in human serum. Further studies are needed to confirm the results of this study.

Levels and distributions of organophosphate flame retardants and plasticizers in sediment from Taihu Lake, China

The concentrations and distribution of seven organophosphate flame retardants and plasticizers (OPs) were investigated in 28 sediment samples collected from Taihu Lake. The analytes were ultrasonically extracted, enriched using solid-phase extraction, and determined by gas chromatography-mass spectrometry. The results indicated that the analytes were all detected in the sediments. The total concentrations of seven OPs ranged from 3.38 to 14.25 µg/kg, and tris (2-chloroiso-propyl) phosphate (TCPP), tris (2-chloroethyl) phosphate (TCEP), and tris (2-butoxyethyl) phosphate (TBEP) were the dominant compounds, with concentrations ranging from<limit of quantification to 2.27 µg/kg, 0.62 to 3.17 µg/kg, and 1.03 to 5.00 µg/kg, respectively. The highest concentration of total assessed OPs (14.25 µg/kg) was found at GH-5, with tris (1,3-dichloro-2-propyl) phosphate (TDCPP) as the main component at the sampling site. This result implied that there is an obvious emission source nearby at Suzhou City; in addition, human activities also play an important role in the concentration of OPs in the sediment.

Measurements of emission factors for primary carbonaceous particles from residential raw‐coal combustion in China

The emission factors (EFs) of particles and their carbonaceous fractions, including black carbon (BC) and organic carbon (OC), are measured for residential burning of coal-chunks. Nine types of coals with wide-ranged thermal maturities were used. Particulate emissions from coal-stove are collected on quartz fiber filters through a dilution sampling system and analyzed for BC and OC by thermal-optical method. The EFs of particulate matter, OC, and BC from bituminous coal burning are 16.77, 8.29, and 3.32 g/kg, respectively, on the basis of burned dry and ash-free (daf) coal mass. They were much higher than those of anthracites, which are 0.78, 0.04, and 0.004 g/kg, respectively. Annual emission inventories of particles, OC, and BC from household coal burning are also estimated based on the EFs and coal consumption. The results of the calculations are 917.8, 477.7, and 128.4 gigagrams (Gg) for total particles, OC, and BC emitted in China during the year 2000.

Concentrations and seasonal variations of polybrominated diphenyl ethers (PBDEs) in in- and out-house dust and human daily intake via dust ingestion corrected with bioaccessibility of PBDEs

The objective of this study was to investigate the concentrations, seasonal variations, bioaccessibility, and associated human daily intake of polybrominated diphenyl ethers (PBDEs) in in- and out-house dust collected in Shanghai, China. The PBDE concentrations varied from 131.6 to 3,886.7 ng g(-1) (with an average of 948.2 ng g(-1)) in in-house dust and from 8.7 to 3,116.3 ng g(-1) (with an average of 290.8 ng g(-1)) in out-house dust during four seasons. The PBDE concentrations in the autumn were the lowest for both in- and out-house dust. Among the detected PBDEs, BDE209 was the predominant congener, accounting for more than 80% of the total PBDE amounts. The bioaccessibility of PBDEs, measured using a simulation system of human gastrointestinal tract, was determined as 14.2-66.4% depending on individual PBDE congeners and showed significant negative correlations with organic matter in dust. After corrected with the bioaccessibility of PBDEs, the human daily intake of PBDEs via dust ingestion was calculated to be 0.4-21.4 and 4.3-40.6 ng day(-1) for an average adult and child in Shanghai, respectively. The values were much lower than most estimates in the literature, in which the bioaccessibility of PBDEs were not taken into account, suggesting that the intake of PBDEs may have been overestimated.

Fractionation and composition of colloidal and suspended particulate materials in rivers

The association of pollutants (nutrients, heavy metals and organic compounds) with colloidal and suspended particle matter (SPM) plays a dominant role in determining their transport, fate, biogeochemistry, bioavailability and toxicity in natural waters. A scheme for the fractionation and composition of colloidal and SPM from river waters has been tested. All four separation methods, i.e. sieving, continuous flow centrifugation, tangential flow filtration, sedimentation field-flow fractionation, were for the first time used to separate five size particulate fractions from river. Significant (gram) amounts of colloidal material (<1 microm) in three size ranges, nominally 1-0.2, 0.2-0.006 and 0.006-0.003 microm were obtained. The separation scheme was able to process large samples (100 l), within reasonable times (1 day) and the apparatus was portable. The aquatic colloid size was also characterized with high resolution by using sedimentation field-flow fractionation technique. The mass-based particle size distribution for the water sample showed a broad size distribution between 0.05 and 0.4 microm with the maximum around 0.14 microm. There was a systematic increase in the content of organic carbon (estimated by loss on ignition), Mg, Ca, Na, Cu and Zn with decreasing particle size, highlighting the importance of the colloidal (<1 microm) fraction. It was concluded that the colloidal Cu and Zn concentrations in rivers might be much higher than those reported before.