常见绿化植物角质层对PAHs的吸附作用

为准确预测萘(Naphthalene,Nap)菲(Phenanthrene,Phe)、芴(Fluorene,Fl)和芘(Pyrene,Pyr)在植物叶面的吸附行为,用化学分离法分离得到马尾松(Pinus massoniana)、海桐(Pittosporum.tobira)、桂花(Osmanthus fragrans)叶面角质层,研究了角质层对Nap、Phe、Fl和Pyr的吸附特征及影响因素。结果表明:3种植物角质层吸收Nap、Phe、Fl和Pyr的作用机理是分配作用。根据线性等温吸附曲线斜率K_d值表明,3种植物角质层对Nap的吸附性能非常强,表现为桂花强于海桐和马尾松;马尾松和桂花对Phe的吸附性能相似,略强于海桐;马尾松对的Fl吸附性能强于桂花和海桐,桂花对Pyr的吸附性能强于马尾松和海桐。通过扫描电镜观测发现,马尾松角质层具有丰富的微观形貌,两侧气孔器排列紧密。桂花角质层表面粗糙呈褶皱状,海桐角质层表面平滑,但两者都未观察到气孔器。植物角质层微观结构的不同是导致植物吸附多环芳烃(polycyclic aromatic hydrocarbons, PAHs)存在种间差异的重要原因。通过傅里叶红外光谱观测显示:海桐、桂花和马尾松在C=O(～1 734 cm~(-1))均有信号,表明其表皮都有明显的酯键吸收峰;3种植物表皮角质层的C-O-C峰(～1 057 cm~(-1))也最为突出,这与其叶片中糖类含量有关。     

Evaluation of genotoxic and non-genotoxic effects of organic air pollution using in vitro bioassays

In this study, organic extracts of total suspended particles (TSP) and the particulate matter (PM) with the size below 2.5 microm (PM(2.5)) combined with organic extracts of the gas phase (GP) collected at two urban and two background localities were analyzed with a bacterial genotoxicity test, SOS chromotest, and an in vitro test for the dioxin toxicity determination, using a modified cell-line of rat hepatoma H4IIE.luc. In addition, the samples of TSP and GP were analyzed for PAHs contents. The PAHs concentrations and both of the toxic activities at the urban localities were much higher than ones at the background localities. Predominantly, traffic was a source of the urban air pollution there which was also confirmed by the evaluation of portions of certain PAHs (BaP/BPE, PYR/BaP) at the localities. On the other hand, the background localities were apparently affected by a long-distance transport of the pollutants from urban and industrial centers. The results of the bioassays indicated potential health risks for the population exposed to the organic air pollutants, especially at the urban localities. Based on the collected samples, distribution of the organic pollutants with the toxic effects in the air was evaluated. The significant portion of the direct genotoxins was bound to the particles larger than 2.5 microm. On the contrary, the indirect genotoxins were bound predominantly to the particles with the size below 2.5 microm. However, in the urban air they may be also bound to the larger particles, as well. While the direct genotoxicity may be related with the presence of PAH-derivatives as well as some polar organic pollutants, the indirect genotoxicity is related with the detected carcinogenic PAHs. But besides the above specified pollutants it is also necessary to consider the presence of other toxic components of the complex organic air pollution mixture that may also show potential health risks. This study demonstrates application of the combination of the screening bioassays for the evaluation of organic air pollution and identification of its health risks.     

玻璃表面PAHs垂向分布特征与室内外对比研究

利用GC-MS对上海市玻璃表面有机膜中PAHs浓度进行了定量分析。结果表明随着楼层的增加,10层居民楼玻璃表面PAHs浓度出现先增加后减少的趋势,最高浓度出现在3层(736 ng/m~2),最低在9层(346 ng/m2);17层公寓楼PAHs浓度则是先减少后增加再减少的趋势,最高浓度出现在9层(2 338 ng/m~2),最低在16层(564 ng/m~2)。TOC与PAHs相关性分析暗示除TOC外,玻璃表面PAHs富集可能还受控于其他因素。10层居民楼主要以3环和4环PAHs为主;而17层公寓楼则以4环为主。玻璃外表面PAHs浓度(555 ng/m~2)远高于内表面(308 ng/m~2);外表面主要以Phe、Pyr、Chry、Fluo和Fl为主;内外表面低环PAHs比值接近于1,高环比值基本上低于0.6。TEQ值虽然较低,但生态风险仍不能忽视。     

Degradation of polycyclic aromatic hydrocarbons by a bacterial consortium enriched from mangrove sediments

The biodegradability of a polycyclic aromatic hydrocarbons (PAHs) mixture consisted of fluorene (Fl), phenanthrene (Phe) and pyrene (Pyr) by a bacterial consortium enriched from mangrove sediments under sediment-free and sediment slurry conditions was investigated. The enriched consortium made up of three bacterial strains, namely Rhodococcus sp., Acinetobacter sp. and Pseudomonas sp., had a good PAH degradation capability with 100% degradation of Fl and Phe in sediment-free liquid medium after 4 weeks of growth. The Fl and Phe degradation percentages in sediment slurry were higher than that in liquid medium. Autochthonous microorganisms in sediments also possessed satisfactory PAH degradation capability and all three PAHs were almost completely degraded after 4 weeks of growth. Bioaugumentation (inoculation of the enriched consortium to sediments) showed a positive effect on PAH biodegradation after 1 week of growth. Complete biodegradation of pyrene took longer time than that for Fl and Phe, indicating the enriched bacterial consortium had preference to utilize low-molecular weight PAHs.     

Sudden high concentration of TSP affected by atmospheric boundary layer in Seoul metropolitan area during duststorm period

Hourly concentrations of TSP, PM(10), PM(2.5) near the surface at Seoul city were examined from March 20 to March 25, 2001 (duststorm event) in order to investigate the effect of a duststorm generated in China on the local aerosol concentration in Korea, The ratios of fine to coarse particles such as TSP to PM(10), TSP to PM(2.5) and PM(10)-PM(2.5) to PM(2.5) showed that a great amount of dust transported from the origin of the duststorm was remarkable with a maximum ratio of 9.77 between TSP and PM(2.5). Back trajectories every 6 h showed the movement of dust particles in the lower atmosphere near 500 m to 1500 m (atmospheric boundary layer), which implied transport from Baotou in inner Mongolia of northern China to the direction of Seoul city in Korea and then the back trajectories passed near the southern border of Mongolia and Baotou through Zengzhou in the midlevels (3000 m) and low levels (500 m) of China, finally reaching Seoul city. So, the TSP concentration at Seoul city was partially influenced by the duststorm, under the prevailing westerly wind and the transported aerosols could influence high concentrations of pollutants of TSP, PM(10) and PM(2.5) in Seoul. The sudden high concentrations of TSP and PM(10) were found for a few hours, especially at 1500 to 1800 LST, March 22. At 1200 LST, before the passage of a cold front through the Korean peninsula, the convective boundary layer (CBL) near Seoul was not shallow, but at 1500 LST, under the frontal passage, the CBL was remarkably thinner (less than 300 m), due to the compression of the boundary layer by the intrusion of cold air. This resulted in the increase of the TSP concentration, even though the mixed layer above maintained almost the same depth. At 1800 LST shortly after the frontal passage, that is, near sunset, the nocturnal cooling of the ground caused air parcels to cool, thereby enhancing the shallower nocturnal surface inversion layer and producing the maximum concentration of TSP of 1388 microg/m(3) near Seoul city.     

Contamination of polycyclic aromatic hydrocarbons (PAHs) in urban soils in Beijing, China

Soil contamination with polycyclic aromatic hydrocarbons (PAHs) is an increasing problem in many countries, including China. An extensive and systematic survey has been undertaken to evaluate the contamination with PAHs of urban soils in Beijing, China. Soil samples were collected from campuses of universities, schools and kindergartens, public squares, fallow land and roadsides, and were analyzed for 16 PAHs by GC-MS. There was a high variability in the total PAHs (SigmaPAHs) concentrations, ranging from less than 366 to 27,825 ng g(-1). The highest SigmaPAHs concentrations were found at roadsides and industrial sites. Soil organic carbon (SOC) is one of the important factors that can influence the concentrations of PAHs in soils. It was found that concentrations of SigmaPAHs were significantly correlated with that of soil organic carbon. To trace the sources of PAHs, the ratios of phenanthrene to anthracene and fluoranthene to pyrene were used to identify pyrogenic and petrogenic sources, respectively. In most cases, PAHs in soils in urban areas of Beijing were pyrogenic. These sources included motor vehicle exhausts, industrial activities and coal burning. These data can be further used to assess the health risk associated with soils polluted with PAHs.     

南京市典型工业区耕地中多环芳烃源解析

多环芳烃作为重要的环境激素类物质，对环境和人类健康具有严重危害而受到人们的广泛重视。选择南京市某一大型钢铁集团周边耕地土壤为研究对象，对研究区域内多环芳烃（PAHs）残留量进行调查，并对其污染来源进行解析，为该区域土壤PAHs的综合防治提供参考依据。结果表明：PAHs总残留量范围为312.2~27 580.9 ng/g，且以4环以上多环芳烃组分为主。单一污染物以芘、屈、荧蒽、苯并［a］芘、蒽、菲、苯并［a］蒽、苯并［k］荧蒽、茚并［1,2,3 cd］芘、苯并［g,h,i］苝为主。不同样区土壤PAHs残留量受常年风向影响明显。推测工业区的气体性排放物是本研究区域土壤中PAHs的主要来源。大气沉降可能是导致本研究区PAHs污染的重要途径之一。另外，地表径流、固体废弃物排放、生活燃煤等导致部分采样点含量较高。在对下风向区域中距中心污染源不同距离采样点PAHs含量分析时发现，高环PAHs总量总体表现出随污染源距离的增加，污染程度递减的规律。在对多环芳烃源成分谱轮廓特征的分析基础上，利用各种参数，从分子量优势度、环数相对丰度、特征指数等方面，分别对各区域土壤中多环芳烃来源进行比较分析，据此推断，四区域PAHs污染均在不同程度上受化石的燃烧所致，但各区域的PAHs污染源不同。钢铁企业内的炼焦厂是该区域多环芳烃主要污染源之一.     

The effects of woodburning on the indoor residential air quality

Data from suburban residences in the Boston metropolitan area reveal a potential adverse impact on indoor air quality from woodburning in woodstoves and fireplaces. Ambient pollutant concentrations at each residence were compared to corresponding pollutant levels indoors at three locations (kitchen, bedroom, and activity room). Individual gaseous pollutant samples were averaged on an hourly basis while 24-h integrated samples of particulate matter were obtained. Ten gaseous pollutants were sampled along with total suspended particulates (TSP). Chemical analyses further determined ten components of TSP including trace metals, benzo-a-pyrene(B)aP, respirable suspended particulates (RSP), and water soluble sulfates and nitrates. Monitoring lasted two weeks at each residence and was conducted under occupied, real-life, conditions. Observed, elevated indoor concentrations of TSP, RSP, and BaP are attributed to woodburning. Data indicate that average indoor TSP concentrations during woodburning periods were about three times corresponding levels during nonwoodburning periods. The primary 24-h national ambient air quality standard (NAAQS) for TSP was exceeded once indoors during fireplace use, and the secondary, 24-h TSP NAAQS, was also exceeded indoors by RSP concentrations. Indoor BaP concentrations during woodstove use averaged five times more than during nonwoodburning periods. At this stage, results are only indicative, but the potential impact from elevated indoor concentrations of TSP, RSP, and BaP, attributed to woodburning, may have long-term health implications.     

The study of Central Taiwan particles concentration variations during earthquake period

Ambient particle concentration was taken on the traffic sampling site over the Chung-Chi Road over the bridge (CCROB) in front of Hungkuang Institute of Technology (HKIT). The sampling time was from August 1999 to December 1999. During the sampling period, Taiwan's biggest earthquake in more than a century registered 7.3 on the Richter scale (Taiwan Chi-Chi Earthquake). Besides, there are more than 20,000 aftershocks following the Taiwan Chi-Chi Earthquake within 3 months. Thus, the mass concentration of particles with aerodynamic diameters smaller than 2.5 microm (PM2.5) and PM2.5-10 was also collected then compared with the total mass concentration of suspended particles (TSP) in this study. The average TSP, PM2.5-10, and PM2.5 concentrations are 106, 24.6, and 58.0 microg/m3, respectively, after the Taiwan Chi-Chi Earthquake. The average TSP concentrations before and after Taiwan Chi-Chi Earthquake were 69.6 and 127 microg/ m3, respectively. In addition, statistical analysis of the PM10 data from this study and EPA in 1999 yielded a Tstatistic of 0.147, which is smaller than t(0.975,18) = 2.101. It is indicated that there was no significant difference. So, the PM10 concentrations measured after Taiwan Chi-Chi Earthquake in this study were also greater than those data previously obtained from Taiwan EPA in the same region of this area. The relationships between TSP, PM10, PM2.5-10, and PM2.5 particle concentrations and wind speed (R2) are .77, .59, .58, .58, respectively. And the ratios of PM2.5/PM25-10, PM2.5/PM10, and PM10/TSP are 221%, 67.2%, 58.0%, respectively. The average ratios of PM2.5/PM2.5-10 and PM2.5/PM10 increase by about 120% and 17%. It indicated that the fine-particles concentration increases compared to the coarse-particles concentration after 921 Taiwan Chi-Chi Earthquake. And the proposed reasons are that local motor vehicle emissions combined the fine particles transported from the Chi-Chi epicenter. More importantly, the wind direction was mainly blown from southeastern part. These two main factors enhance the fine-particles concentration in this area.     

Shorter sperm telomere length in association with exposure to polycyclic aromatic hydrocarbons: Results from the MARHCS cohort study in Chongqing,China and in vivo animal experiments

It has been well demonstrated that polycyclic aromatic hydrocarbons (PAHs) can cause reproductive toxicity, and shorter telomere length in sperm may be one of the factors causing male infertility. However, whether exposure to PAHs is associated with sperm telomere length (STL) has never been evaluated. The present study aimed to assess the potential association between PAHs exposure and STL, and to explore potential biomarkers that may predict the effects of low-level exposure to PAHs on human sperm. Questionnaires and biological samples were collected from 666 volunteers participating in the Male Reproductive Health in Chongqing College Students (MARHCS) cohort study in 2014. Semen parameters were measured for 656 participants, while urinary PAH metabolites, STL and sperm apoptosis were successfully measured for 492, 444 and 628 participants, respectively. The linear regression analysis revealed that increased levels of urinary 1-hydroxypyrene (1-OHPyr) and 1-hydroxynapthalene (1-OHNap) were associated with decreased STL (− 0.385; 95% CI, − 0.749, − 0.021 for 1-OHPyr; and − 0.079; 95% CI, − 0.146, − 0.011 for 1-OHNap). The significant negative associations remained after adjusting for potential confounders. However, no significant associations were observed between urinary PAH metabolites and semen quality or sperm apoptosis. We also administrated rats with benzo[a]pyrene (B[a]P; 0, 1, 5, and 10 mg/kg) for 4 weeks and found shorter STL and decreased telomerase expression in germ cells in a dose-dependent manner. In conclusion, environmental exposure to some PAHs may be associated with decreased human STL, and the in vivo animal results also demonstrate the adverse effects of B[a]P on telomere of male germ cells.     

Climate change impact on the PAH photodegradation in soils: Characterization and metabolites identification

Polycyclic aromatic hydrocarbons (PAHs) are airborne pollutants that are deposited on soils. As climate change is already altering temperature and solar radiation, the global warming is suggested to impact the environmental fate of PAHs. This study was aimed at evaluating the effect of climate change on the PAH photodegradation in soils. Samples of Mediterranean soils were subjected to different temperature and light radiation conditions in a climate chamber. Two climate scenarios were considered according to IPCC projections: 1) a base (B) scenario, being temperature and light intensity 20 °C and 9.6 W/m², respectively, and 2) a climate change (CC) scenario, working at 24 °C and 24 W/m², respectively. As expected, low molecular weight PAHs were rapidly volatilized when increasing both temperature and light intensity. In contrast, medium and high molecular weight PAHs presented different photodegradation rates in soils with different texture, which was likely related to the amount of photocatalysts contained in both soils. In turn, the hydrogen isotopic composition of some of the PAHs under study was also investigated to verify any degradation process. Hydrogen isotopes confirmed that benzo(a)pyrene is degraded in both B and CC scenarios, not only under light but also in the darkness, revealing unknown degradation processes occurring when light is lacking. Potential generation pathways of PAH photodegradation by-products were also suggested, being a higher number of metabolites formed in the CC scenario. Consequently, in a more or less near future, although humans might be less exposed to PAHs, they could be exposed to new metabolites of these pollutants, which might be even more toxic.     

Measurements and analysis of criteria pollutants in New Delhi, India

Ambient concentrations of carbon monoxide (CO), nitrogen oxides (NOx), sulfur dioxide (SO2), and total suspended particulates (TSP) were measured from January 1997 to November 1998 in the center of downtown [the Income Tax Office (ITO) located on B.S.G. Marg] New Delhi, India. The data consist of 24-h averages of SO2, NOx, and TSP as well as 8 and 24-h averages of CO. The measurements were made in an effort to characterize air pollution in the urban environment of New Delhi and assist in the development of an air quality index. The yearly average CO, NOx, SO2, and TSP concentrations for 1997 and 1998 were found to be 4810+/-2287 and 5772+/-2116 microg/m3, 83+/-35 and 64+/-22 microg/m3, 20+/-8 and 23+/-7 microg/m3, and 409+/-110 and 365+/-100 microg/m3, respectively. In general, the maximum CO, SO2, NOx, and TSP values occurred during the winter with minimum values occurring during the summer, which can be attributed to a combination of meteorological conditions and photochemical activity in the region. The ratio of CO/NOx (approximately 50) indicates that mobile sources are the predominant contributors for these two compounds in the urban air pollution problem in New Delhi. The ratio of SO2/NOx (approximately 0.6) indicates that point sources are contributing to SO2 pollution in the city. The averaged background CO concentrations in New Delhi were also calculated (approximately 1939 microg/m3) which exceed those for Eastern USA (approximately 500 microg/m3). Further, all measured concentrations exceeded the US National Ambient Air Quality Standards (NAAQS) except for SO2. TSP was identified as exceeding the standard on the most frequent basis.     

Distribution of pesticides, PAHs and heavy metals in prawn ponds near Kolleru lake wetland, India

This paper discussed the distribution of pesticides, polycyclic aromatic hydrocarbons (PAHs) and heavy metals in water, sediment and prawn from intensive prawn ponds (n=8) near the Kolleru lake wetland, India and assessed the quality of prawn for human consumption and also discussed the possible effects of these pollutants on pond environment and aquatic environment. The chemicals and other products used in prawn ponds near the Kolleru lake wetland were documented. The sediment, prawn and water samples were collected six times from selected prawn ponds during the production period of 3 months. Water samples were analyzed for selected physico-chemical parameters. The levels of pesticides, PAHs and heavy metals were found to decrease in the order sediment followed by prawn and water. The maximum concentrations of pesticides in sediment, prawn and water were alpha-BHC (174.2 microg g(-)(1)), gamma-BHC (234 microg g(-)(1)), malathion (256 microg g(-)(1)), chloripyrifos (198.5 microg g(-)(1)), endosulfan (238 microg g(-)(1)), dieldrin (19.6 microg g(-)(1)) and p,p'-DDT (128.6 microg g(-)(1)). Isodrin was found below detectable limit. The maximum concentrations of PAHs in sediment, prawn and water are anthracene (0.901 microg kg(-)(1)), fluranthene (0.601 microg kg(-)(1)), pyrene (0.786 microg kg(-)(1)), chrysene (0.192 microg kg(-)(1)), benzo(a)pyrene (0.181 microg kg(-)(1)) and benzo(ghi)perylene (227 microg kg(-)(1)). Benzo(e)pyrene, perylene, isomers of dibenzoanthracene and coronene were found below detectable limits. The maximum concentrations of heavy metals in sediment, prawn and water and also in prawn feed are Cu (791 microg g(-)(1)), Pb (270 microg g(-)(1)), Cd (1.07 microg g(-)(1)), Mn (4417 microg g(-)(1)), Ni (8.1 microg g(-)(1)), Co (5.8 microg g(-)(1)), Zn (1076 microg g(-)(1)), Cr (36.4 microg g(-)(1)), As (2.9 microg g(-)(1)), Se (6.3 microg g(-)(1)), Th (2.1 microg g(-)(1)) and Mo (0.762 microg g(-)(1)).     

Induction of EROD activity in European eel (Anguilla anguilla) experimentally exposed to benzo[a]pyrene and beta-naphthoflavone

The induction of liver ethoxyresorufin O-deethylase (EROD) activity was investigated in the European eel, Anguilla anguilla, collected from a Mediterranean brackish environment and experimentally exposed to benzo[a]pyrene (B[a]P) and beta-naphthoflavone (BNF). Eels were injected intraperitoneally at increasing doses (0.1, 1, 10, and 50 mg/kg wet body weight) using corn oil as a carrier and sacrificed after 7 days. The main objectives of the present study are: (1). to assess of the sensitivity of EROD induction as a biomarker to polycyclic aromatic hydrocarbon (PAH) exposure; (2). to determine an EROD dose-response relationship of the contaminants used; and (3). to compare the efficiency of B[a]P and BNF as inducers of EROD activity. Results showed that both chemicals resulted in a dose-dependent EROD induction, but increases were not linear. EROD activity seemed to reach a plateau at the exposure of 10 mg/kg in both treatment groups; B[a]P was a more potent inducer than BNF was at the higher doses (10 and 50 mg/kg), while the opposite result was observed at the lower ones (0.1 and 1 mg/kg). The greatest induction occurred in eels treated with 10 mg/kg B[a]P, in which a 261-fold increase in EROD activity was observed. Results showed that EROD activity in A. anguilla is significantly induced by B[a]P and BNF exposure, responding to a wide range of concentrations of these contaminants. We infer that this tool may be suited as a diagnostic biomarker for biomonitoring PAHs pollution in Mediterranean brackish environments and further field research is suggested.     

Wintertime indoor air levels of PM10, PM2.5 and PM1 at public places and their contributions to TSP

From 26 October 2002 to 8 March 2003, particulate matter (PM) concentrations (total suspended particles [TSP], PM10, PM2.5 and PM1) were measured at 49 public places representing different environments in the urban area of Beijing. The objectives of this study were (1) to characterize the indoor PM concentrations in public places, (2) to evaluate the potential indoor sources and (3) to investigate the contribution of PM10 to TSP and the contributions of PM2.5 and PM1 to PM10. Additionally, The indoor and outdoor particle concentrations in the same type of indoor environment were employed to investigate the I/O level, and comparison was made between I/O levels in different types of indoor environment. Construction activities and traffic condition were the major outdoor sources to influence the indoor particle levels. The contribution of PM10 to TSP was even up to 68.8%, while the contributions of PM2.5 and PM1 to PM10 were not as much as that of PM10 to TSP.     

Residues and source identification of persistent organic pollutants in farmland soils irrigated by effluents from biological treatment plants

Sewage and industrial effluents from biological treatment plant have been widely used for agricultural irrigation in north part of China. However, effluents after biological treatment still contain heavy metals and persistent organic contaminants. The persistent organic contaminants accumulated in soil may transfer through the food chains and cause adverse health effects on human or biological effects on soil fauna and flora after long-term application. In present study, field surveys were carried out in the farmlands irrigated by effluents from biological treatment plants that receive sewage wastewater and industrial discharges. Residues of polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) in the soils irrigated using both ground water and effluents were compared. The origins of PAHs in the soils were discussed. The results showed that wastewater irrigation could cause accumulation of PAHs in soils close to the pollution discharge. Significantly higher concentrations of PAHs were observed in the sampling sites close to the entrance of main channel in contrast to those along branches and the reference sites. There was no significant relationship between the accumulation of persistent organic pollutants and organic matter content in soil (TOC). Soil contamination of these persistent organic pollutants as affected by effluent irrigation was characterized by the dominant accumulation of high-molecular-weight PAHs (HMW-PAHs). In the case study, concentration of benzo[a]pyrane (BaP, 45.6 ng/g), indeno[1,2,3-cd]pyrene (IcP, 86.3 ng/g), benzo[g,h,i]perlene (BgP, 66.9 ng/g) could exceed the limits of the soil quality standard for biodegraded soils. In identification of the sources, the IcP/BgP values of PAHs in soils were more close to that in air particulates from coal/coke source (1.09+/-0.03 ng/g) [Dickhut RM, Canuel EA, Gustafson KE, Liu K, Arzayus KM, Walkers E, et al. Automotive sources of carcinogenic polycyclic aromatic hydrocarbons associated with particulate matter in the chesapeake bay region. Environ Sci Technol 2000;34:4635-40]. Therefore, both of the PAHs residues in effluents and emission from a nearby coal/coke plant were responsible. Also in this case study, low levels of the OCPs were observed and were not of significant concern in this wastewater irrigation area. Among the different OCPs analyzed, DDTs (mean 8.41 ng/g) and HCHs (mean 2.91 ng/g) were the major components. From the ratios of DDT/DDTs and beta-HCH/HCHs, it indicated that OCPs residues should be from historical usage.     

Composition, sources, and potential toxicological significance of PAHs in the surface sediments of the Meiliang Bay, Taihu Lake, China

Twenty-five surface sediment samples were collected from Meiliang Bay, Taihu Lake, China, in 2003. The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs), identified as priority pollutants by the USEPA, were determined by gas chromatography equipped with a mass spectrometry detector (GC-MS). Total concentrations of the PAHs ranged from 1207 to 4754 ng/g dry weight. Sediment samples with the highest PAH concentrations were from the northern site of the bay, which is in proximity to the incoming PAH source; the PAH levels in the southern part were relatively low. The observed PAH levels were higher than those in river sediments in China but were lower than those found in sediments of urban areas and harbors. According to the observed molecular indices, PAHs originated largely from the high-temperature pyrolytic process, whereas the petrogenic process was more commonly responsible for PAH contamination in harbors. A good correlation existed between the benzo[a]pyrene level and the total PAH concentration (r=0.97), making benzo[a]pyrene a potential molecular marker for PAH pollution. According to the numerical effect-based sediment quality guideline (SQGs) of the United States, the levels of PAHs at most studied sites in Meiliang Bay, except some sites in the northern part of the bay, should not exert adverse biological effects. In the northern part of the bay, the PAH levels at sites 21 and 22 exceed the effects range low (ERL) and could thus cause acute biological impairments, in comparison with the sediment quality guidelines. The total PAH levels were expressed as the B[a]P toxicity equivalents (TEQs(carc)) and compared to the contaminated sediments from Guba Pechenga, Barents Sea, Russia.     

红枫湖地表水中多环芳烃的分布及来源

将固相微萃取与气相色谱联用，对贵阳红枫湖水样中16种美国环境保护署优控的多环芳烃进行分析。结果表明：红枫湖水中16种多环芳烃总量为0167 1~0336 4 μg/L，与国内其它水系相比，湖中存在多环芳烃轻度污染。7种（萘、荧蒽、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、茚并(1,2,3-cd)芘和苯并(ghi)苝）多环芳烃的总量未超出中国城市供水行业对多环芳烃规定的限值，但作为饮用水源，红枫湖水中的苯并(a)芘含量已超出我国标准GB3838-2002中生活饮用水地表水源地的苯并(a)芘限值，并且苯并(a)蒽、〖JX-*9〗〖SX（B-25x〗〖HT7，5”〗艹〖〗〖HT6”，5”〗屈〖HT5”〗〖SX）〗〖JX*9〗、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、茚并(1,2,3-cd)芘的含量也超过了美国环境保护署地表水水质标准限值。通过多环芳烃特征参数的比值，分析了红枫湖水中多环芳烃的污染来源。污染源分析表明，湖中多环芳烃的主要来源为燃烧源，包括木材、煤以及化石燃料的燃烧，同时也有一部分多环芳烃是来源石油类物质的输入.     

红枫湖地表水中多环芳烃的分布及来源

将固相微萃取与气相色谱联用，对贵阳红枫湖水样中16种美国环境保护署优控的多环芳烃进行分析。结果表明：红枫湖水中16种多环芳烃总量为0167 1~0336 4 μg/L，与国内其它水系相比，湖中存在多环芳烃轻度污染。7种（萘、荧蒽、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、茚并(1,2,3-cd)芘和苯并(ghi)苝）多环芳烃的总量未超出中国城市供水行业对多环芳烃规定的限值，但作为饮用水源，红枫湖水中的苯并(a)芘含量已超出我国标准GB3838-2002中生活饮用水地表水源地的苯并(a)芘限值，并且苯并(a)蒽、〖JX-*9〗〖SX（B-25x〗〖HT7，5”〗艹〖〗〖HT6”，5”〗屈〖HT5”〗〖SX）〗〖JX*9〗、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、茚并(1,2,3-cd)芘的含量也超过了美国环境保护署地表水水质标准限值。通过多环芳烃特征参数的比值，分析了红枫湖水中多环芳烃的污染来源。污染源分析表明，湖中多环芳烃的主要来源为燃烧源，包括木材、煤以及化石燃料的燃烧，同时也有一部分多环芳烃是来源石油类物质的输入.     

Mutagenicity, genotoxicity and carcinogenic risk assessment of indoor dust from three major cities around the Pearl River Delta

The mutagenicity and genotoxicity of workplace dust including commercial office, secondary school, shopping mall, hospital, electronics factory and manufacturing plant in Hong Kong and settled house dust from Hong Kong, Shenzhen and Guangzhou were measured. Results indicated that indoor dust contained both frameshift and base pair substitution mutagens. Dust from manufacturing plant showed highest mutagenic potency on TA98±S9 and TA100±S9 activation, whereas, electronics factory showed highest genotoxicity with and without S9 activation. TA100 (-S9) mutagenic potency was significantly correlated with genotoxicity expressed as SOSIP (-S9) of workplace dust (r(2)=0.37, p<0.01). The total PAHs concentration of settled house dust from PRD ranged from 1.63 to 29.2μg/g. Linear regression analyses indicated that the PAHs likely accounted for about 45% of the TA98 with S9 mutagenic activity of workplace dust. TA98 (-S9) mutagenicity (r(2)=0.27, p<0.05) and SOSIP (-S9) of house dust (r(2)=0.41, p<0.01) were both significantly correlated with the number of inhabitants in the house. To achieve a more accurate cancer risk assessment, the oral bioaccessibility of B(a)A, Chry, B(b+k)F, B(a)P, D(ah)A and I(cd)P in different dust ranging from 1.3% to 17% was taken into account. Risk assessments indicated that about 26% of house dust samples resulted in unacceptable cancer risk (>1×10(-6)) for preschool children.