The sedimentary fluxes of polycyclic aromatic hydrocarbons in the Yangtze River Estuary coastal sea for the past century

Polycyclic aromatic hydrocarbons (PAHs) in two (210)Pb dated sediment cores from the coastal East China Sea, strongly influenced by the discharge from the Yangtze River, were determined to help to reconstruct the economic development over the past century in East China. The variations in PAH concentrations and fluxes in the sediment cores were primarily due to energy structure change, severe floods and dam construction activities. The impact on PAHs by the river discharge overwhelmed the atmospheric depositions. The profiles of PAH fluxes and concentrations as well as compositions in the cores revealed the transformation from an agricultural economy to an industrial one especially after the 1990s' in the region. PAHs in the study area were dominated by pyrolytic sources.     

Source apportionment of polycyclic aromatic hydrocarbons (PAHs) in surface sediments of the Huangpu River, Shanghai, China

We applied cluster analysis and principal component analysis (PCA) with multivariate linear regression (MLR) to apportion sources of polycyclic aromatic hydrocarbons (PAHs) in surface sediments of the Huangpu River in Shanghai, China, based on the measured PAH concentrations of 32 samples collected at eight sites in four seasons in 2006. The results indicate that petrogenic and pyrogenic sources are the important sources of PAHs. Further analysis shows that the contributions of coal combustion, traffic-related pollution and spills of oil products (petrogenic) are 40%, 36% and 24% using PCA/MLR, respectively. Pyrogenic sources (coal combustion and traffic related pollution) contribute 76% of anthropogenic PAHs to sediments, which indicates that energy consumption is a predominant factor of PAH pollution in Shanghai. Rainfall, the monsoon and temperature play important roles in the distinct seasonal variation of PAH pollution, such that the contamination level of PAHs in spring is significantly higher than in the other seasons.

Brief

We apportion PAHs in surface sediments of the Huangpu River and show that coal combustion, traffic-related pollution, and petroleum spillage are the major sources.     

The residual dynamic of polycyclic aromatic hydrocarbons and organochlorine pesticides in fishponds of the Pearl River delta, South China

Hong Kong and South China are the most developed regions within China. The industrialization in these areas has resulted in severe environmental problems. Sediment and biotic samples including tilapia (Oreochromis mossambicus), bighead carp (Aristichthys nobilis), grass carp (Ctenopharyngodon idellus), crucian carp (Carassius auratus) and mandarin fish/fresh water grouper (Siniperca chuatsi) were collected from different fishponds in the Pearl River Delta (Tanzhou, Sanjiao, Guangzhou, Shipai, Changan and Mai Po) for the analysis of polycyclic aromatic hydrocarbons (PAHs) and organochlorine (OC) pesticides. Mandarin fish, which belongs to the highest trophic level, accumulated the highest concentrations of PAHs and DDTs among all fish species. The levels of DDTs in fish samples ranged from 1.5 to 62ng g-1 (wet wt.), with more than 30% of the fish samples exceeding the limit of 14.4ng g-1 (wet wt.) for human consumption recommended by US EPA (2000). Levels of PAHs in fish samples ranged from 1.91 to 224.03ng g-1 (wet wt.), but the potency-weighted total concentrations of PAHs in all muscle tissues were below the guideline value of 0.67ng g-1 (wet wt.) for human consumption set by US EPA (2000). The guideline value calculated was based on a tissue consumption rate of 142.2g day-1 (4-5 meals per week), which is a more protective rate for populations with a high consumption of fish, like Chinese and Asians. The effect of lipid content in PAHs and DDTs accumulation in fish tissue was not significant in general.     

Photolysis of polycyclic aromatic hydrocarbons in water

The decomposition of benzo[a]pyrene (BAP), chrysene (CHR) and fluorene (FLU) in an aqueous solution by means of photolysis has been studied. The influence of initial polycyclic aromatic hydrocarbons' (PAHs) concentration, pH of the reaction mixture, temperature, presence of oxygen and tert-butyl alcohol (t-BuOH) on the degradation rate has been observed. BAP and CHR are decomposed by a mechanism different than FLU. Quantum yields of the photolytic decomposition of BAP, CHR and FLU were determined and equal 0.014, 0.0031 and 0.0038, respectively.     

Precipitation scavenging of polycyclic aromatic hydrocarbons in Mumbai, India

The concurrent rain and air sampling was conducted for thirteen rain events between the last week of May and end of June 2001. Concentration of total PAHs varied from 84.25 to 777.49 ng/l whereas that in air was in the range of 4.05 to 34.42 ng/m(3). In rainwater the lower molecular weight PAHs (e.g. Phenanthrene, Fluoranthene and Pyrene) were found to be more prominent than the higher molecular weight compounds. The gas phase scavenging ratio (Wg) was found to increase with the molecular weight of the compound. The particle phase scavenging ratio (Wp) values for the more volatile PAHs were generally much higher than those for less volatile PAHs. The higher MW PAHs have Wg values equal to or larger than their Wp values.     

Particle-associated polycyclic aromatic hydrocarbons in the atmospheric environment of Zonguldak, Turkey

Airborne fine (PM(2.5)) and coarse (PM(2.5-10)) particulate matter was collected from January to December in 2007 in Zonguldak, Turkey using dichotomous Partisol 2025 sampler. Fourteen selected polycyclic aromatic hydrocarbons (PAHs) in particulate matter were determined simultaneously by high-performance liquid chromatography with fluorescence detection (HPLC-FL) and seasonal distributions were examined. The source identification of PAHs in airborne particulates was performed by principal component analysis (PCA) in combination with diagnostic ratios. The predominant PAHs determined in PM(2.5) were pyrene, fluoranthene, benzo[a]anthracene, chrysene, benzo[b]fluoranthene and benzo[a]pyrene. The total concentrations of PAHs were up to 464.0 ng m(-3) in fine and 28.0 ng m(-3) in coarse fraction in winter, whereas in summer times were up to 22.9 and 3.0 ng m(-3) respectively. Approximately 93.3% of total PAHs concentration was determined in PM(2.5) in winter and 84.0% in summer. The concentration levels of PAHs fluctuate significantly within a year with higher means and peak concentrations in the winter compared to that of summer times. Higher benzo(a)pyrene-equivalent (BaPE) concentrations of PAHs were obtained for PM(2.5) especially in winter. The results obtained from PCA in combination with diagnostic ratios revealed that coal combustion and vehicle emissions were the major pollutant sources for both PM(2.5) and PM(2.5-10) associated PAHs in studied area. Two principal components for PM(2.5) and three for PM(2.5-10) were identified and these accounted for 89.4 and 85.2% of the total variance respectively. The emissions from coal combustion were estimated to be the main source of PAHs in the ambient air particulates with contributions of 80.8% of total variance for PM(2.5) and 53.8% for PM(2.5-10).     

Distributions of polycyclic aromatic hydrocarbons in surface waters, sediments and soils of Hangzhou City, China

Ten polycyclic aromatic hydrocarbons (PAHs) were simultaneously measured in 17 surface water samples and 11 sediments of four water bodies, and 3 soils near the water-body bank in Hangzhou, China in December 2002. It was observed that the sum of PAHs concentrations ranged from 0.989 to 9.663 microg/L in surface waters, from 132.7 to 7343 ng/g dry weight in sediments, and from 59.71 to 615.8 ng/g dry weight in soils. The composition pattern of PAHs by ring size in water, sediment and soil were surveyed. Three-ring PAHs were dominated in surface waters and soils, meanwhile sediments were mostly dominated by four-ring PAHs. Furthermore, PAHs apparent distribution coefficients (K(d)) and solid f(oc)-normalized K(d) (e.g. K(oc)= K(d) / f(oc)) were calculated. The relationship between logK(oc) and logK(ow) of PAHs for field data on sediments and predicted values were compared. The sources of PAHs in different water bodies were evaluated by comparison of K (oc) values in sediments of the river downstream with that in soils. Hangzhou section of the Great Canal was heavily polluted by PAHs released from industrial wastewater in the past and now PAHs in sediment may serve as sources of PAHs in surface water. PAHs in Qiantang River were contributed from soil runoff. Municipal road runoff was mostly contributed to West Lake PAHs.     

Seasonal variation, sources and gas/particle partitioning of polycyclic aromatic hydrocarbons in Guangzhou, China

Air samples were collected weekly at an urban site and a suburban site in Guangzhou City, China, from April 2005 to March 2006, to measure the concentrations of polycyclic aromatic hydrocarbons (PAHs) in the ambient air and study their seasonal variations, gas/particle partitioning, origins and sources. The concentrations of ∑ 16-PAHs (particle + gas) were 129.9 ± 73.1 ng m⁻³ at the urban site and 120.4 ± 48.5 ng m⁻³ at the suburban site, respectively. It was found that there was no significant difference in PAH concentrations between the urban and suburban sites. Seasonal variations of PAH concentrations at the two sampling sites were similar, with higher levels in the winter that gradually decreased to the lowest levels in the summer. The average concentrations of ∑ 16-PAHs in the winter samples were approximately three times higher than those of the summer samples because in the summer local emissions dominated, and in the winter the contribution from outside sources or transported PAHs is increased. The plot of logK_p versus logP_L⁰ for the data sets of summer and winter season samples had significantly different slopes at both sampling sites. The slopes for the winter samples were steeper than those for the summer samples. It was also observed that gas/particle partitioning of PAHs showed different characteristics depending on air parcel trajectories. Steeper slopes were obtained for an air parcel that traveled across the continent to the sampling site from the northern or northeastern sector, whereas shallower slopes were obtained for air masses that traveled across the sea from the southern or eastern sector. Diagnostic ratio analytical results imply that the origins of PAHs were mainly from petroleum combustion and coal/biomass burning. The anthracene/phenanthrene and benzo[a]anthracene/chrysene ratios in the winter were significantly lower than those in the summer, which indicate that there might be long-range transported PAH input to Guangzhou in the winter.     

Wet deposition of polycyclic aromatic hydrocarbons in The Netherlands

The concentrations of 11 polycyclic aromatic hydrocarbons (PAH) in rainwater at four locations in the Netherlands in 1983 are reported. From literature data for these PAH in air, scavenging ratios were calculated. For PAH predominantly adsorbed on aerosols these scavenging ratios are in the range 3-13 X 10(4). For phenanthrene the scavenging ratios are in the range 0.35-2.5 X 10(4). The data for the aerosol-associated PAH at the various locations are discussed in terms of aerosol in-cloud scavenging, and are compared with reported data from Belgium and Germany. The scavenging ratios for phenanthrene are compared with those predicted on the basis of Henry's law constant and were found to be less than one order of magnitude higher than expected, possibly because of enhanced aqueous solubility.     

Spatial and temporal distribution of polycyclic aromatic hydrocarbons (PAHs) in the atmosphere of Xiamen, China

An intensive sampling program was conducted from October 2008 to September 2009 at the five different environmental sites in Xiamen, Fujian Province, to study the spatial and temporal characteristics of Polycyclic Aromatic Hydrocarbons (PAHs) in the gaseous and particulate phase, respectively. The PAHs concentrations at different sites were quite distinct during four seasons. The average concentrations of PAHs in winter were about 8.4 times higher than those in spring, and the concentrations of background were 0.56 times lower than those of industrial area. In addition, the higher temperature in summer affected the particle/gas partitioning of PAHs and led to the higher concentrations of gaseous PAHs. Diagnostic ratios of PAHs, which were employed to indicate the primary sources of PAHs in Xiamen, showed that the traffic vehicle exhaust was the largest contributor and the primary source for PAHs in Xiamen, especially in urban area; while the stationary combustion processes, such as petrochemical factories and power plants, were mainly responsible for PAHs sources in the industrial areas. The health risk of PAHs in the particulate phase was higher than those of the gaseous phase at the five sampling sites. The average toxic equivalent (BaP_eq) of the benzo[a]pyrene values for PAHs were 0.14, 0.32, 1.38 and 3.59 ng m^− 3 in spring, summer, autumn and winter, respectively. Furthermore, the results of average BaP_eq in all four seasons indicated that the health risks of particulate PAHs were higher than those of the gaseous PAHs at different sampling sites.     

Distribution of polycyclic aromatic hydrocarbons in snow of Mount Nanshan,Xinjiang

Polycyclic aromatic hydrocarbon (PAH) in snow samples collected from Mount Nanshan (Xinjiang, China) was investigated for eight stations. Fourteen PAHs were detected in these samples. The total PAH concentration ranged from 70.15 ng/L to 155.67 ng/L, with an average of 113.02 ng/L. Human carcinogens, such as fluoranthene, chrysene, benzo(a)pyrene, dibenzo(a,h)anthracene, indeno(1,2,3‐cd)pyrene and benzo(ghi)perylene in snow were assessed based on risk quotient. Preliminary assessment showed that these PAHs posed a moderate risk. Component analysis showed that the PAHs found in the snow samples were mainly three‐ring PAHs, which comprised 34.51–90.81% of the total PAHs. Phenanthrene, fluorene and anthracene accounted for 35.08, 11.90 and 11.13% of the total PAHs, respectively. The ΣPAH content increased with the increasing altitude, and the highest concentration of 155.67 ng/L was observed in snow samples from the N7 station, which was located near the top of the mountain. This high PAH concentration in N7 was possibly due to more frequent human activities in the area and long‐distance transportation of PAHs. Isomer ratios were used to determine the possible sources of PAHs in the samples. The results indicate that coal and biomass combustion made a larger contribution than emissions from petroleum consumption. It is therefore of utmost importance to develop new fuels taking the place of coal and to achieve as complete as possible for the burning of carbon‐containing materials.     

Chemical and photochemical degradation of polycyclic aromatic hydrocarbons in the atmosphere

Results of studies on chemical and photochemical transformations of polycyclic aromatic hydrocarbons (PAH) are reviewed. Various parameters may modify the kinetics of these reactions, such as light intensity, concentration of gaseous pollutants (NO_x, SO_x, O₃), chemico-physical characteristics of particulates or substrates into which the PAH are adsorbed. Depending on these variables, the half-life of BaP varies from 10 to 104 300 min. The possibility of artefact formation during sampling is discussed. The necessity of clarifying mechanisms for these phenomena, in order to correctly evaluate the risks for exposed populations, is emphasized.     

Levels and patterns of polycyclic aromatic hydrocarbons in incineration ashes

Polycyclic aromatic hydrocarbons were analysed in weathered bottom ash from municipal solid waste incineration, fly ash from a mixed heating plant and an ash mixture from different kinds of biofuels. Although of different origin and age, all three ashes are evaluated in different small-scale fill applications. The ultimate goal is the usage of these ashes on a larger scale. The samples were Soxhlet extracted and analysed using GC/MS in the full scan mode. The sum of the 16 US EPA PAHs was found to vary from 140 microg/kg up to more than 77000 microg/kg. Total amounts of PAHs were similar in bottom ash and in fly ash. The concentration in the mixed biofuel ash was more than 10 times higher, and exceeded the generic guidelines for PAHs in soil set by the Swedish Environmental Protection Agency. The patterns of the individual PAHs normalised to the total concentration of PAHs were found to be very similar for all the three ashes. Naphthalene and phenanthrene were the dominating PAHs for all ash samples, but the mixed biofuel ash also contained high levels of fluoranthene and pyrene.     

Health risk assessment on dietary exposure to polycyclic aromatic hydrocarbons (PAHs) in Taiyuan, China

Twenty-five kinds of seven categories of foods were sampled in December 2008 and the concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) were determined. The highest level of total PAHs was detected in pork (195.30 ng/g) whereas the lowest concentration was found in milk (8.73 ng/g). The median values of B[a]P equivalent (B[a]P_eq) daily exposure doses for children, adolescents, adults and seniors of male were estimated to be 392.42, 511.01, 571.56 and 532.56 ng/d, respectively, whereas those for the above population groups of female were found to be 355.16, 440.51, 487.64 and 444.85 ng/d, respectively. The incremental lifetime cancer risk (ILCR) values at the 22.1th, 26.1th, 12.7th, 24.9th, 22.7th, 27.0th, 12.9th, and 25.5th percentiles for male children, male adolescents, male adults, male seniors, female children, female adolescents, female adults and female seniors, respectively, were larger than 10^− 6, indicating high potential carcinogenic risk, and were larger than 10^− 4 at the 74.5th, 78.7th, 60.6th, 77.4th, 75.3th, 79.5th, 60.8th and 77.9th percentiles for the above groups, respectively, which implied significant cancer risk. Sensitivity analysis found that the two variables of oral cancer slope factor of benzo(a) pyrene (SF) and the daily dietary PAH exposure level (ED) had the greater impact than that of body weight (BW) on the ILCR.     

The environmental load and cycle of polycyclic aromatic hydrocarbons

Many polycyclic aromatic hydrocarbons (PAH) are known to be carcinogenic to animals and probably to man. Therefore, a better understanding of their formation, behavior and fate in the environment is necessary. Of the PAH carcinogens, 3,4-benzpyrene (BaP), which constitutes only about 1 % – 20 % of the group, is one of the most potent and ubiquitous, and therefore the most widely studied. Although the risk from carcinogenic PAH cannot yet be estimated, synergistic effects with other substances have also to be considered.The formation of PAH in the environment is due to an endogenic synthesis by microorganisms, phytoplankton, algae and highly developed plants, which provide the natural background, and to a second process which is connected with man-controlled high temperature pyrolitic reactions, open burning, and natural volcanic activities. Photooxidation is the major decomposition process by which PAH are reduced, biodegradation by microorganisms being a secondary reduction mechanism.The worldwide production of PAH by biosynthesis cannot be estimated on the basis of the limited data available at present. However, the global emission of BaP derived from exogenous sources has been estimated at about 5000 tons per year, a quantity which appears to exceed that formed endogenically. It may be assumed, that until the beginning of this century there still existed a natural balance between the production and degradation of PAH, which kept the natural background concentration low and fixed. However, with the ever-increasing industrial development in many parts of the world the natural balance is being disturbed and the production rate of PAH is constantly rising, while their rate of decomposition remains more or less constant. In view of the carcinogenic characteristics of many PAH compounds, their concentration in the environment should be considered alarming and efforts should be made to reduce or even eliminate them wherever possible. At the same time, an environmental programme should be developed for monitoring the PAH compounds and the various parameters affecting their formation, retention and destruction.     

Emission of polycyclic aromatic hydrocarbons from animal carcass incinerators

This study investigated two batch-type animal carcass waste incinerators, one in a hog farm (HOWI) and the other in a livestock disease control centre (LIWI). Additionally, a medical waste incinerator (MEWI) with a fixed grate for the disposal of biological medical waste was also examined. A GC/MS technique was applied to analyze the concentrations of 21 polycyclic aromatic hydrocarbons (PAHs) species in the stack flue gas, bottom ash and wet scrubber (WSB) effluent. The analytical results indicated that total-PAHs in the stack flue gas for HOWI, LIWI and MEWI were mainly in the gaseous phase. Moreover, the mean total-PAHs concentrations of the stack flue gas for HOWI and LIWI were 1.5 and 1.4 times higher than for MEWI (=391 microg/m(3)), respectively. At the most carcinogenic potencies, the results revealed that the mean BaP+BbF+DBA concentrations in the stack flue gas for HOWI and LIWI were 7.6 and 4.6 times higher than those of MEWI (=1.18 microg/m(3)), respectively. Moreover, during the outbreak of foot-and-mouth disease among pigs in southern Taiwan in 1997, emissions of total-PAHs and BaP+BbF+DBA exceeded 226.2 and 2.3 kg/day, respectively.     

Vertical distribution and anaerobic biodegradation of polycyclic aromatic hydrocarbons in mangrove sediments in Hong Kong, South China

The vertical distribution of polycyclic aromatic hydrocarbons (PAHs) at different sediment depths, namely 0-2 cm, 2-4 cm, 4-6 cm, 6-10 cm, 10-15 cm and 15-20 cm, in one of the most contaminated mangrove swamps, Ma Wan, Hong Kong was investigated. It was the first time to study the intrinsic potential of deep sediment to biodegrade PAHs under anaerobic conditions and the abundance of electron acceptors in sediment for anaerobic degradation. Results showed that the total PAHs concentrations (summation of 16 US EPA priority PAHs) increased with sediment depth. The lowest concentration (about 1300 ng g^− 1 freeze-dried sediment) and the highest value (around 5000 ng g^− 1 freeze-dried sediment) were found in the surface layer (0-2 cm) and deeper layer (10-15 cm), respectively. The percentage of high molecular weight (HMW) PAHs (4 to 6 rings) to total PAHs was more than 89% at all sediment depths. The ratio of phenanthrene to anthracene was less than 10 while fluoranthene to pyrene was around 1. Negative redox potentials (Eh) were recorded in all of the sediment samples, ranging from − 170 to − 200 mv, with a sharp decrease at a depth of 6 cm then declined slowly to 20 cm. The results suggested that HMW PAHs originated from diesel-powered fishing vessels and were mainly accumulated in deep anaerobic sediments. Among the electron acceptors commonly used by anaerobic bacteria, sulfate was the most dominant, followed by iron(III), nitrate and manganese(IV) was the least. Their concentrations also decreased with sediment depth. The population size of total anaerobic heterotrophic bacteria increased with sediment depth, reaching the peak number in the middle layer (4-6 cm). In contrast, the aerobic heterotrophic bacterial count decreased with sediment depth. It was the first time to apply a modified electron transport system (ETS) method to evaluate the bacterial activities in the fresh sediment under PAH stress. The vertical drop of the ETS activity suggested that the indigenous bacteria were still active in the anaerobic sediment layer contaminated with PAHs. The biodegradation experiment further proved that the sediment collected at a depth of 10-15 cm harbored anaerobic PAH-degrading bacterial strains (two Sphingomonas, one Microbacterium, one Rhodococcus and two unknown species) with some intrinsic potential to degrade mixed PAHs consisting of fluorene, phenanthrene, fluoranthene and pyrene under low oxygen (2% O₂) and non-oxygen (0% O₂) conditions. This is the first paper to report the anaerobic PAH-degrading bacteria isolated from subsurface mangrove sediment.     

Quantification of polycyclic aromatic hydrocarbons in soil at McMurdo Station, Antarctica.

Polycyclic aromatic hydrocarbons (PAHs) are a group of compounds that have attracted much attention over the past several years. The United States Environmental Protection Agency (USEPA) has identified numerous PAHs as known or probable human carcinogens. The quantity of PAHs in the environment has dramatically increased, with the majority emitted from fossil fuel combustion sources. Surface soil samples were collected at McMurdo Station, Antarctica (77 degrees 51S, 166 degrees 41E), during peak summer activity and analyzed for PAHs. PAHS were detected at several locations, with maximum concentrations for naphthalene, acenaphthene, acenaphthylene, and fluoranthene at 27,000, 17,800, 15,700 and 13,300 mg/kg, respectively. Results suggest anthropogenic activities may be contributing to increased levels of PAHs present in McMurdo soils.     

Emission characteristics of polycyclic aromatic hydrocarbons from combustion of different residential coals in North China

Emission properties of polycyclic aromatic hydrocarbons (PAHs) from combustion of six residential coals in North China were investigated. The results indicated that, the total emission factors (EFs) for 15 PAH species in gaseous and particulate phases ranged from 52.8 to 1434.8 mg/kg with a decreasing sequence of local bituminous coals and anthracite coals, and honeycomb briquettes were largely dependent on the raw coals used to produce them. Particulate phase, dominated by median or high molecular weight components, made a major contribution (68.8% - 76.5%) to the total EFs for bituminous coals, while gaseous phase with principal low molecular weight species accounted for most (86.3% - 97.9%) of the total EFs for anthracite coals. The phase partitioning of PAH emission for honeycomb briquettes was similarly dependent on the crude coals. The total EFs, phase partitioning and component profiles of emitted PAHs were mainly influenced by the inner components of the studied coals. Burning mode and flue number on household coal-stoves also affected the emission characteristics by means of the oxygen supply. A sum of seven carcinogenic PAHs, benzo(a)pyrene(BaP)-equivalent carcinogenic power and total toxicity potency expressed in 2,3,7,8-tetrachlorodibenzo-dioxin(TCDD) toxic equivalence exhibited that bituminous coals and produced honeycomb briquettes had remarkably elevated values. Fluoranthene, benzo(b)fluoranthene, benzo(k)fluoranthene, chrysene and indeno(1,2,3-cd)pyrene from anthracite coals showed higher levels of BaP-based toxic equivalent factor, though the other toxicity indices were rather low for this type of coal.     

The exposure of temple workers to polycyclic aromatic hydrocarbons

Five temples, each a different size, were selected for this study. Two of the temples were located in Taichung City (in central Taiwan), and three were in Tainan City (in Southern Taiwan). Aerosols smaller than 10 microm aerodynamic diameter (PM(10)) were collected by using personal collection samplers during pilgrim days (the first and fifteenth day of each lunar month) and normal days (all other days). Regression analysis showed that about 1.6 microg/m(3) of PM(10) contributed to the workers' exposure in the temples for each joss stick increase in the censer. The concentrations of total polycyclic aromatic hydrocarbons (t-PAHs) and carcinogenic PAHs (car-PAHs) on pilgrim days were higher than those on normal days. Mean concentrations of urinary 1-hydroxypyrene (1-OHP) in the pre-shift and post-shift workers of the five temples on normal days were 1.20 and 1.61 microg/g creatinine, respectively. Furthermore, the post-shift concentrations of 1-OHP in the workers of temples on pilgrim days were all higher than those of the workers of corresponding temples on normal days. Significant relationships between the urinary concentrations of 1-OHP and the exposure concentrations of pyrene, total PAHs and BaP(eq) were found in the workers of the temples. Results of linear regression showed that the increase of unit concentration (1 ng/m(3)) of pyrene led to a 0.05 microg/g creatinine increase of urinary 1-OHP, while the increase of unit concentration (1 ng/m(3)) of BaP(eq) resulted in an increase of 0.03 microg/g creatinine of urinary 1-OHP.