Gene J. Zheng

Relationships between tissue concentrations of polycyclic aromatic hydrocarbons and antioxidative responses of marine mussels, Perna viridis.

Local mussels, Perna viridis, were transplanted from a relatively clean site to various polluted sites in Hong Kong. After a 30-day field exposure, different antioxidant parameters including glutathione S transferase (GST), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR), NADPH DT-diaphorase (DT-d), glutathione (GSH) and lipid peroxidation were quantified, and tissue concentrations of benzo[a]pyrene (B[a]P) as well as a total of five polycyclic aromatic hydrocarbons (PAHs) with potential carcinogenicity were determined for individual mussels. Results indicated that: (1) tissue concentrations of B[a]P and total PAHs from the same site were highly variable; (2) gill SOD, DT-d and lipid peroxidation showed no response to tissue pollutants; (3) the majority of the antioxidant parameters were induced by increasing tissue pollutant concentrations; and (4) amongst the various parameters, oxyradical scavenger GSH best correlated with tissue concentrations of pollutants.

Relationships between tissue concentrations of chlorinated hydrocarbons (polychlorinated biphenyls and chlorinated pesticides) and antioxidative responses of marine mussels, Perna viridis.

Marine mussels, Perna viridis, were transplanted from a reference site to various polluted sites around Hong Kong. After 30 d of exposure, antioxidative responses in the gills and hepatopancreas and tissue concentrations of chlorinated hydrocarbons [polychlorinated biphenyls (PCBs) and chlorinated pesticides (CPs)] were determined for individual mussels. Glutathione S transferase (GST) and glutathione (GSH) were positively correlated with tissue PCB concentrations. Only one of the enzymatic antioxidants, glutathione peroxidase (GPx), showed significant response to tissue PCB. No significant correlation was found between tissue concentrations of chlorinated hydrocarbons and other enzymatic antioxidants (superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR) and NADPH DT-diaphorase (DT-d). Oxidative stress, measured as thiobarbituric acid reactive substances, was correlated with chlorinated pesticide concentrations in tissues. This study demonstrated a correlation between GST/ GSH and chlorinated hydrocarbons. The apparent lack of correlation between trace organic pollutants and some of the enzymatic antioxidants may be due to the inhibitory effects caused by these chemicals. The above results suggest that more investigations are needed before these enzymes can be used as biomarkers.

Petroleum hydrocarbons and polycyclic aromatic hydrocarbons (PAHs) in Hong Kong marine sediments

Abstract A total of 20 surficial sediment samples, obtained from Hong Kong coastal waters, were analysed for petroleum hydrocarbons (PHCs) and a suite of 15 polycyclic aromatic hydrocarbons (PAHs). The results indicate that Hong Kong coastal sediments are often seriously polluted with petroleum related hydrocarbons. This is especially so in heavily urbanised or industrialized localities, such as Kowloon Bay (Victoria Harbour), Tsing Yi North and Tolo Harbour. Petroleum hydrocarbon pollutants in marine sediments are believed to be mainly derived from the transportation of oil, shipping activities, spillages, and industrial, stormwater and wastewater discharge. The ratio of unresolved complex mixture (UCM) to n -alkanes, carbon preference index (CPI), and n -C 16 values indicate that the main contribution to petroleum hydrocarbon contamination is via oil and its products. Pollutant sources appear to be stable and continuing when compared with previous data.

Persistent toxic substances in remote lake and coastal sediments from Svalbard, Norwegian Arctic: Levels, sources and fluxes

Surface sediments from remote lakes and coastal areas from Ny-Alesund, Svalbard, Norwegian Arctic were analyzed for polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs). Relatively high levels of PAHs were encountered from several lakes from Ny-Alesund, which were within the range of levels reported for European high mountain lakes and some urban/industrialized areas in the world, pointing to the role of remote Arctic lakes as potential reservoir of semi-volatile organic compounds. Specific patterns of PBDEs were observed, showing higher concentrations of lower brominated compounds such as BDE-7, 17 and 28. Estimated surface sediment fluxes of PAHs in Ny-Alesund remote lakes were similar to those observed for some European high mountain lakes. The current PAH levels in sediments from three lakes exceeded Canadian sediment quality guidelines, suggesting the presence of possible risks for aquatic organisms and the need for further studies.

Chlorinated hydrocarbon contaminants in Hong Kong surficial sediments.

Twenty surficial sediments were sampled from nearshore Hong Kong waters during 1997-1998, and analyzed for a range of chlorinated pesticides and polychlorinated biphenyls (PCBs). Results showed that concentrations (on a dry weight basis) of total HCHs were in the range 0.1-16.7 ng g-1, and total DDTs 0.3-14.8 ng g-1. PCBs, measured as an Aroclor 1242, 1248, 1254, 1260 (1:1:1:1) mixture, were found to be in a range of 0.5-97.9 ng g-1, and were at highest concentrations in Victoria Harbour. Results indicated that chlorinated pesticides and PCBs in Hong Kong nearshore sediments were most likely derived from waste discharge from a variety of sources, including agricultural, sewage, industrial waste disposal and shipping-related activities. In addition, as the north and west sides of Hong Kong are subject to influence from the Pearl River (due mainly to agricultural activities in the Pearl River Delta, and to a lesser extent developments around the Shenzhen Special Economic Zone), these inputs are also thought to be likely sources of contamination.

Distribution and sources of polycyclic aromatic hydrocarbons in the sediment of a sub-tropical coastal wetland.

Sediment cores (0-35cm below surface) from twelve sampling stations in the Mai Po and Inner Deep Bay Ramsar Site of Hong Kong were retrieved in the period March-December 1999. Vertical profiles of 15 priority polycyclic aromatic hydrocarbons (PAHs) in each sediment core were determined. Ranges of total PAH concentration, [sigmaPAH], in the wetland sediment were 0.18-0.83 (N = 0.36) microg/g dried sediment (mudflats) and 0.63-0.96 (x = 0.77) microg/g dried sediment (mangroves). A decreasing trend in depth averaged [sigmaPAH] was observed from the landward end towards the seaward end of the Marshes. On the mudflats, vertical profiles of the PAHs were quite uniform. At the fringe of the Mai Po mangroves, significantly higher concentration of all PAHs was observed at the upper 0 to -8 cm layer. No significant difference in the distribution patterns of the 15 priority PAHs in summer and winter was observed. This indicates that distribution of PAHs in the sediment of the Mai Po Marshes is not very sensitive to sub-tropical climatic changes of the region. Two PAH isomer ratios, [Phen]/([Phen] + [Anthra]) and [Pyrene]/([Pyrene] + [Fluoran]), were used to identify potential sources of PAH contamination in the wetland. Results revealed that local deposition is a more important source than long-range atmospheric transportation.

Asia-Pacific mussel watch for emerging pollutants: Distribution of synthetic musks and benzotriazole UV stabilizers in Asian and US coastal waters

We analyzed 68 green and blue mussels collected from Cambodia, China, Hong Kong, India, Indonesia, Japan, Korea, Malaysia, Philippines, Vietnam and the USA during 2003 and 2007, to elucidate the occurrence and widespread distributions of emerging pollutants, synthetic musks and benzotriazole UV stabilizers (BUVSs) in Asia-Pacific coastal waters. Synthetic musks and BUVSs were detected in mussels from all countries, suggesting their ubiquitous contamination and widespread distribution. High concentrations of musks and BUVSs were detected in mussels from Japan and Korea, where the levels were comparable or greater than those of PCBs, DDTs and PBDEs. Significant correlations were found between the concentrations of HHCB and AHTN, and also between the concentrations of UV-327 and UV-328, which suggest similar sources and compositions of these compounds in commercial and industrial products. To our knowledge, this is the first study of large-scale monitoring of synthetic musks and BUVSs in Asia-Pacific coastal waters.

Relationship between tissue concentrations of polycyclic aromatic hydrocarbons and DNA adducts in green-lipped mussels (Perna viridis)

Green-lipped mussels (Perna viridis) were collected from a site in Hong Kong which is relatively free from polycyclic aromatic hydrocarbon (PAH) contamination, and maintained in situ at this and three other sites with different degrees of PAH contamination. The transplanted mussels were retrieved after a 30-day field exposure. DNA adducts in the gill tissues were quantified, and tissue concentrations of benzo[a]pyrene as well as total PAHs (with potential carcinogenicity) determined for individual mussels. Results indicate that (1) tissue concentration of PAHs and adduct levels in mussels collected from a single site can be highly variable; and (2) adduct levels were related to tissue concentrations of benzo[a]pyrene as well as total PAHs of individual animals.

The use of muscle burden in rabbitfish Siganus oramin for monitoring polycyclic aromatic hydrocarbons and polychlorinated biphenyls in Victoria Harbour, Hong Kong and potential human health risk

Muscle concentrations of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) were determined in rabbitfish Siganus oramin collected from Victoria Harbour and its vicinity, Hong Kong from 2004 to 2007. Spatially, relatively higher levels of [summation operator]PAH (1.05-4.26 microg g(-1)) and [summation operator]PCB (45.1-76.9 ng g(-1)) were determined in the central and western sites inside the harbour. Temporally, upward trend of [summation operator]PAH, accompanied with a proportion shift from high molecular weight to low molecular weight PAHs, was detected during the three-year study period, suggesting a heavier marine traffic in Victoria Harbour and its western region. However, human health risk assessment based on five individual PAHs indicated that PAHs in fish muscles posed minimal health risk through consumption. In contrast, a downward trend of [summation operator]PCB was registered as the open use of PCBs has been banned. Despite this, the level of [summation operator]PCB in fish muscles still posed a health risk on the local people who have a high fish consumption rate. While seasonal influences on [summation operator]PAH/[summation operator]PCB accumulation in S. oramin seemed to be negligible, our findings in S. oramin were in line with the established PAH and PCB levels in sediments and/or mussels from the harbour, suggesting S. oramin can be used as a model fish species for monitoring PAHs and PCBs in the region.

Bioaccumulation and historical deposition of polybrominated diphenyl ethers (PBDEs) in Deep Bay, South China

To characterize the bioaccumulation and historical trends of polybrominated diphenyl ethers (PBDEs) in Deep Bay, an important water body between Hong Kong and main land China with a Ramsar mangrove wetland (Maipo), marine organisms and core sediments were collected to determine their PBDEs concentrations. Sediment core dating was accomplished using the (210)Pb method. PBDEs concentrations in fish ranged from 0.17 to 4.16 ng g(-1) wet wt., with a mean value of 2.00 ng g(-1) wet wt. Temporal trends of the target PBDE congeners levels in core sediment generally increased from 1948 to 2003, with the highest levels in top sediment, suggesting an ongoing PBDEs input. The average sedimentation flux of PBDEs was 0.25 ng cm(-2) a(-1), and the double time of total PBDEs concentration was ca. 12.3 a. Correlations between the biota-sediment accumulation factors (BSAF) of PBDEs and their corresponding octanol-water partition coefficient (K(ow)) were discussed.