Risk assessments of PAHs and Hg exposure via settled house dust and street dust, linking with their correlations in human hair.

Domestic energy, chemicals bioaccessibility and particle size were found as three critical factors for risk assessment of PAHs exposure via settled house dust (SHD) and street dust. ∑PAHs and Hg contained in SHD were significantly (p<0.01) higher in coal-burning households of Qingyang (8.45-121; 0.48-16.4 µg g(-1)) than households in Guangzhou (1.23-22.2; 0.004-10.6 µg g(-1)) and 90% coal-burning houses were estimated with unacceptable cancer risks (>10(-4)) via SHD exposure. The highest accumulation trend of PAHs and Hg were found in <63 µm particles, and different particle sizes resulted in large variations of the obtained risks (up to 10 fold). Bioaccessibility corrected PAHs led to a significant decrease on related cancer risks and decreased in the order of 1.9, 1.1, 0.6 and 0.4 µg g(-1) with the increase of particle sizes (<63, 63-100, 100-280, 280-2000 µm). Scalp hair was tested as an indicator of body burdens of PAHs (0.05-0.9 µg g(-1)) and Hg (0.04-1.6 µg g(-1)). Different PAHs profiles were found between PAHs in SHD and those of hair, indicating that exogenous exposure to PAHs adsorbed on dust was not the major source of hair PAHs.

Exposure assessment and distribution of polychlorinated biphenyls (PCBs) contained in indoor and outdoor dusts and the impacts of particle size and bioaccessibility.

The size fraction, bioaccessibility and associated human daily intake of PCBs via indoor and outdoor dust collected from two most populated urban centers of Pearl River Delta (PRD), China, were studied. The ΣPCBs levels (ng g(-1)) in indoor (51.9-264) and outdoor (4.02-228) dust in Guangzhou (GZ) were found higher than those in indoor (17.4-137) and outdoor (7.75-114) dust of Hong Kong (HK). Hexa-PCB was the largest contributor in dust samples (29-64%), followed by tri-PCB. The size fraction of PCBs indicated a high accumulation effect of particles less than 63 µm, while the lowest was found in 280-2000 µm. Toxic equivalency (TEQ) of dioxin-like PCBs in indoor dust of GZ and HK was 2 to 13 times higher than that in outdoor dust. The bioaccessibility of PCBs was determined as 5-61% depending on individual PCB congeners under study and bioaccessible PCB exposure was significantly lower than the estimate for total PCB. The daily intake of bioaccessible PCBs via dust ranged in 0.02-8.95 and 0.37-17.8 ng day(-1) in GZ while 0.01-4.95 and 0.16-9.83 ng day(-1) in HK for adults and children, respectively. Dust ingestion contributed to 0.49-10.6% of overall non-dietary PCB exposure (dust ingestion and inhalation) for adults while 12.9-35% for children, indicating the dominant contribution from inhalation.

Polybrominated diphenyl ethers and polychlorinated dibenzo-p-dioxins and dibenzofurans in surface dust at an E-waste processing site in Southeast China.

Surface dust collected from printed circuit board recycling workshop floors, roads, a schoolyard, and an outdoor food market in Guiyu, China, a village intensely involved in e-waste processing, were investigated for levels of polybrominated diphenyl ethers (PBDEs) and polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). PBDE concentrations in dust from workshop-floors (14,800 ± 5130 ng/g) and on adjacent roads to the workshops (24,900 ± 31,600 ng/g) were highest among the study sites whereas PCDD/F concentrations were highest at the schoolyard (1316 pg/g) and in a workshop (1264 pg/g). Analyses of <2 mm and <53 µm dust particle sizes did not show any significant differences in PBDE concentrations. The cytotoxicity was investigated using two bioassays: 7-ethoxyresorufin O-deethylase (EROD-TEQ) and MTT. EROD-TEQ values ranged from 260 to 432 pg/g, with the highest in dust collected from a street lined with workshops. Using the MTT assay, cytoxicity of dust from the plastic chips drying district in Guiyu was higher than dust from the other sites investigated. This study showed that the primitive recycling of e-waste introduced toxic pollutants into the environment which are potentially harmful to the health of e-waste workers and local residents, especially children, and warrants an urgent investigation into POPs related health impacts.

[Occurrence and distribution of organotin compounds in Thais clavigera from Xiamen coast].

Occurrence and distribution of 6 organotin compounds including butyltin and phenyltin species were detected in Thais clavigera which were collected from 9 coastal areas sites around Xiamen Coast, by pentylized derivatization, GC-FPD. Results indicated that all Thais clavigera samples were contaminated with organotin compounds. The concentrations in Thais clavigera soft bodies varied from 0.3 to 70.6 ng x g(-1) with a mean value of 28.8 ng x g(-1) for butyltin compounds, and from nd to 18.8 ng x g(-1) with a mean value of 7.9 ng x g(-1) for phenyltin compounds, respectively. MBT and TPhT were high levels in butyltin compounds and phentyltin compounds, respectively. In addition, butyltin compounds were the dominant contaminates in all samples with high percentage from 74.3% to 96.8%. There was a significant correlation between TBT and TPhT (R2=0.7109, p<0.01). This result showed that both TBT and TPhT came from antifouling paints for ships or for mariculture nets. Compared with those data reported from the other regions around southeast coast of China, present study reveals that contaminated level of organotin compounds in Thais clavigera are relatively lower in Xiamen Coast. But it is higher than those in 2002.

Distribution and behavior of trace metals in the sediment and porewater of a tropical coastal wetland.

Vertical profiles (0-30 cm below surface) of four trace metals-Cadmium (Cd), Chromium (Cr), Lead (Pb) and Zinc (Zn)-in the sediment and sediment porewater of an ecologically important intertidal mudflat in the Mai Po and Inner Deep Bay Ramsar Site were thoroughly studied over a period of 10 months (from March 1999 to January 2000). Two surveys, one in summer and another in winter, involving a total of eight sampling stations were conducted to study the seasonal variation of the remobilization characteristics of these trace metals in the mudflat sediment. The range of depth averaged concentration of these trace metals in the mudflat sediment was: 0.3-0.8 microg/g (Cd); 9.8-91.0 microg/g (Cr); 7.3-69.1 microg/g (Pb); and 39.5-192.0 microg/g (Zn), while that in the sediment porewater was: 0.3-121.1 microg/l (Cd); 3.0-2704.1 microg/l (Cr); 2.6-105.6 microg/l (Pb); and 32.6-4238.3 microg/l (Zn). In general, levels of dissolved trace metals in the sediment porewater were much higher in the summer than in the winter while their concentrations in the sediment were more or less the same throughout the year. Enrichment of Cd, Pb and Zn in the sediment porewater of the upper oxic layer and that of Cr in the oxic-sub-oxic boundary was generally observed. Regions in the vicinity of the Mai Po mangroves and the river mouths of Shenzhen River and Shan Pui River were found to be hotspots of trace metal pollution. Benthic diffusive fluxes of trace metals from the mudflat sediment were also estimated. Of the four trace metals, cadmium showed the greatest tendency toward remobilization from the sediment phase to the more bio-available porewater phase.

Petroleum hydrocarbons and polycyclic aromatic hydrocarbons in the surficial sediments of Xiamen Harbour and Yuan Dan Lake, China.

Surficial sediments were sampled from nine stations in Xiamen Harbour and two stations in Yuan Dan Lake during April 2002. Sediment samples were extracted by organic solvents, separated by silica gel column chromatography and analyzed by gas chromatography-mass selective detector (GC-MSD). Selected ion monitoring was at M/Z=57 for petroleum hydrocarbons (PHCs) and individual M/Zs for each of the 15 typical polycyclic aromatic hydrocarbons (PAHs) and nine alkylated PAHs. The results showed that concentrations of PHCs and total PAHs in the sediments of Yuan Dan Lake were 1397 microg g(-1) (dry weight, dw) and 1377 ng g(-1) (dw), respectively. The ranges for PHCs and total PAHs in the sediments from Xiamen Harbour were 133-943 microg g(-1) (dw) and 98-309 ng g(-1) (dw), respectively. Shipping activities, industrial wastewater discharges, fuel oil spillage from ships and vehicles were the main sources of PHCs and PAHs in the Harbour. In addition, the widespread use of coal for industrial processes and domestic consumption accounted for the second largest source of PAHs in the sediments, while atmospheric transport and deposition of PAHs are also important.

Asia-Pacific mussel watch: monitoring contamination of persistent organochlorine compounds in coastal waters of Asian countries.

Contamination of persistent organochlorines (OCs) such as PCBs (polychlorinated biphenyls), DDT and its metabolites (DDTs), HCH (hexachlorocyclohexane) isomers (HCHs), chlordane compounds (CHLs), and HCB (hexachlorobenzene) were examined in mussels collected from coastal waters of Asian countries such as Cambodia, China, Hong Kong, India, Indonesia, Japan, Korea, Malaysia, Philippines, Far East Russia, Singapore, and Vietnam in 1994, 1997, 1998, 1999, and 2001 to elucidate the contamination status, distribution and possible pollution sources and to assess the risks on aquatic organisms and human. OCs were detected in all mussels collected from all the sampling sites investigated. Considerable residue levels of p,p(')-DDT and alpha-HCH were found in mussels and the concentrations of DDTs and HCHs found in mussels from Asian developing countries were higher than those in developed nations suggesting present usage of DDTs and HCHs along the coastal waters of Asian developing countries. On the other hand, lower concentrations of PCBs detected in mussels from Asian developing countries than those in developed countries indicate that PCBs contamination in mussels is strongly related to industrial and activities. To our knowledge, this is a first comprehensive report on monitoring OCs pollution in the Asia-Pacific region.

Asia-Pacific mussel watch: monitoring of butyltin contamination in coastal waters of Asian developing countries.

Butyltin compounds (BTs) including mono-, di-, and tributyltin and total tin (sigmaSn), were determined in green mussels (Perna viridis) from various Asian developing countries, such as Cambodia, China (Hong Kong and southern China), Malaysia, India, Indonesia, the Philippines, and Vietnam, to elucidate the contamination status, distribution, and possible sources and to assess the risks on aquatic organisms and humans. Butyltin compounds were detected in green mussels collected from all the sampling location investigated, suggesting widespread contamination of BTs along the coastal waters of Asian developing countries. Among butyltin derivatives, tributyltin (TBT) was the predominant compound, indicating its ongoing usage and recent exposures in Asian coastal waters. Higher concentrations of BTs were found in mussels collected at locations with intensive maritime activities, implying that the usage of TBT as a biocide in antifouling paints was a major source of BTs. In addition, relatively high concentrations of BTs were observed in mussels from aquaculture areas in Hong Kong and Malaysia, as it has been reported in Thailand. With the recent improvement in economic status in Asia, it is probable that an increase in TBT usage will occur in aquaculture. Although contamination levels were generally low in mussel samples from most of the Asian developing countries, some of those from polluted areas in Hong Kong, India, Malaysia, the Philippines, and Thailand revealed levels comparable to those in developed nations. Furthermore, the concentrations of TBT in some mussels from polluted areas exceeded the threshold for toxic effects on organisms and estimated tolerable average residue levels as seafoods for human consumption. A significant correlation was observed between the concentrations of sigmaBTs and sigmaSn in mussels, and sigmaBTs were made up mostly 100% of sigmaSn in mussels taken from locations having intensive maritime/human activities. This suggests that anthropogenic BTs represent the major source of tin accumulation in mussels. To our knowledge, this is a first comprehensive report on butyltin pollution monitoring in developing countries in the Asia-Pacific region.