Measurement and source identification of polycyclic aromatic hydrocarbons (PAHs) in the aerosol in Xi'an, China, by using automated column chromatography and applying positive matrix factorization (PMF)

In this study, we measured polycyclic aromatic hydrocarbons (PAHs) in aerosols in Xi'an, China from 2005 to 2007, by using a modified Soxhlet extraction followed by a clean-up procedure using automated column chromatography followed by HPLC/fluorescence detection. The sources of PAHs were apportioned by using the positive matrix factorization (PMF) method. The PM₁₀ concentration in winter (161.1 ± 66.4 μg m^− 3, n = 242) was 1.5 times higher than that in summer (110.9 ± 34.7 μg m^− 3, n = 248). ΣPAH concentrations, which are the sum of the concentrations of all detected PAHs, in winter (344.2 ± 149.7 ng m^− 3, n = 45) was 2.5 times higher than that in summer (136.7 ± 56.7 ng m^− 3, n = 24) in this study. These strong seasonal variations in atmospheric PAH concentration are possibly due to coal combustion for residential heating. According to the source apportionment with PMF method in this study, the major sources of PAHs in Xi'an are categorized as (1) mobile sources such as vehicle exhaust that constantly contribute to PAH pollution, and (2) stationary sources such as coal combustion that have a large contribution to PAH pollution in winter.     

Organochlorines and mercury in livers of great cormorants (Phalacrocorax carbo sinensis) wintering in northeastern Mediterranean wetlands in relation to area, bird age, and gender

Wild birds are exposed to pollutants in their habitats. Top consumers of aquatic environments such as the fish-eating great cormorant (Phalacrocorax carbo sinensis) are especially affected due to the bioaccumulation of toxic substances in their tissues. This study analysed the livers of 80 great cormorants from Greece to estimate the concentration of organochlorines and mercury and to examine their possible toxic effects and origin. The results showed that mercury (geometric mean 8089 ng g⁻¹ dw), p,p′-DDE (2628 ng g⁻¹ dw), ∑ HCHs (47 ng g⁻¹ dw) and HCB (116 ng g⁻¹ dw) concentrations can be considered high compared with those found in great cormorant livers elsewhere except in highly polluted areas, whereas ∑ PCBs occurred in relatively low concentrations (1091 ng g⁻¹ dw). β-HCH was the dominant HCH isomer. Pollutant levels were generally unrelated to area, age and gender. However, p,p′-DDE and p,p′-DDD showed intersite differences, whilst the proportion of PCBs with 8 chlorine atoms were significantly higher in adult than 1st year great cormorants. Pollution did not reflect local patterns but rather these along the Baltic and Black Seas, whilst differences in p,p′-DDE concentration and ∑ DDTs/∑PCBs ratios between Evros, Axios or Amvrakikos, found on common migration route, suggested different bird origins. Most birds had toxic mercury concentrations; 83.7% above 4000 ng g⁻¹ dw and 16% above 17,000 ng g⁻¹ dw. Other pollutant levels were too low to have adverse effects.     

Behavior, mass inventories and modeling evaluation of xenobiotic endocrine-disrupting chemicals along an urban receiving wastewater river in Henan Province, China

Historically, the locations of cities mainly depend on the available water source and the urban river not only supplies the fresh water to city but also receives its wastewaters. To analyze the influences of urban zone on its receiving water river, the Jialu River in Henan Province, China, a typical urban river was chosen. Water and sediment samples were collected along the river in 2007 to analyze the concentrations of xenobiotic endocrine-disrupting chemicals (XEDCs) including nonylphenol (NP), octylphenol (OP) and bisphenol A (BPA) in surface water and sediment. The results showed that the concentrations of OP, NP and BPA in surface water were 20.9-63.2 ng L⁻¹ (mean 39.8 ng L⁻¹), 75.2-1520 ng L⁻¹ (mean 645 ng L⁻¹), 410-2990 ng L⁻¹ (mean 1535 ng L⁻¹), respectively. The lowest and highest concentrations of XEDCs in surface water were found in the upper stream and downstream of Zhengzhou urban zone, which was regarded as the major discharge source of these chemicals to this river. The concentrations of OP, NP and BPA in the sediment were 15.9-31.1 ng g⁻¹, 145-349 ng g⁻¹ and 626-3584 ng g⁻¹ with the average concentrations of 21.4 ng g⁻¹, 257 ng g⁻¹ and 2291 ng g⁻¹, respectively. The results of in situ sediment-water partition of XEDCs showed that the partition coefficients (log K_oc′) in the downstream were higher than that in the upstream, which was mainly caused by the retransfer of surface sediment from the upper stream to the downstream. Comparison of measured and theoretical inventories of XEDCs in sediment indicated that the residual time of XEDCs in sediment in the river was about 5 years, which was in the same order of magnitude with its big flood frequency. In order to predict concentration variances of XEDCs in surface water, a fugacity-hydrodynamic model was developed according to the concept of in series completely stirred tank reactors (CSTR). The model results showed that about 29-65% of XEDCs derived from the urban zone (about 2.0 t yr⁻¹) would finally dissipate from aqueous phase in the 170 km downstream of the river. Assuming the discharge amount of XEDCs from the urban zone remaining constant, the predicted concentrations of the total XEDCs in the over 90% river reach would be higher than 1.0 μg L⁻¹ under all normal, high water and low water season in 2007.     

Polycyclic aromatic hydrocarbons (PAHs) in urban surface dust of Guangzhou, China: Status, sources and human health risk assessment

Ninety-six urban surface dust samples collected from Guangzhou, a typical urban center in South China, were analyzed for 16 PAHs (2-6 rings). ∑ PAHs concentrations in the urban surface dust ranged from 0.84 to 12.3 μg/g with a mean of 4.80 μg/g. High molecular weight compounds (4-6 rings) contributed to 62 to 94% of ∑ PAHs mass in the surface dust samples. Four hotspots with highest ∑ PAHs were identified via kriging prediction mapping, representing the highly-urbanized regions: central downtown, highway and industrial area. Two major origins of PAHs inputs to urban surface dust were identified as vehicle emissions (51.9%) and coal combustion (26.8%). The 95% UCL of Incremental Lifetime Cancer Risk (ILCR) due to human exposure to urban surface dust PAHs in central South China was 3.03 × 10⁻⁶ for children and 2.92 × 10⁻⁶ for adults.     

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 ∑PAH (1.05-4.26 μg g^− 1) and ∑PCB (45.1-76.9 ng g^− 1) were determined in the central and western sites inside the harbour. Temporally, upward trend of ∑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 ∑PCB was registered as the open use of PCBs has been banned. Despite this, the level of ∑PCB in fish muscles still posed a health risk on the local people who have a high fish consumption rate. While seasonal influences on ∑PAH/∑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.     

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.     

Distributions of total mercury and methylmercury in surface sediments and fishes in Lake Shihwa, Korea

The concentrations of total mercury (THg) and methylmercury (MeHg) in the sediments of Lake Shihwa, an artificial salt lake in Korea located near two large industrial complexes, were determined to investigate the state of Hg contamination in the lake sediments and the effect of local Hg source. THg and MeHg concentrations in the sediments, monitored for 2 years, ranged from 0.02 to 0.28 µg g^− 1 and ≤ 0.026 to 0.67 ng g^− 1, respectively. The overall distribution of Hg in lake sediments showed higher values near industrial complexes and in the central part of the lake. However, the correlations between Hg and environmental factors, such as organic material (OM) content, and acid volatile sulfide (AVS), were weak and did not clearly explain the variation in Hg distribution. The spatial distribution of sediment Hg and monthly precipitation data during the sampling period showed that the amount of runoff following rain events and water gate operation may be additional important factors regulating Hg level and distribution in lake sediments. The levels of THg in fish species in this lake ranged from 9.8 to 35 ng g^− 1, suggesting that the bioavailability of sediment Hg in the lake may be low. Although the THg concentrations in Lake Shihwa sediment were lower than those in other foreign study sites, they were higher than in neighboring coastal regions, and are constantly increasing. This result indicates that the nearby industrial complexes may be the major source of Hg found in the sediments of Lake Shihwa.     

Size distribution and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in aerosol particle samples from the atmospheric environment of Delhi, India

Ambient aerosol particles were collected using a five-stage impactor at six different sites in Delhi. The impactor segregates the TSPM into five different sizes (viz. > 10.9, 10.9-5.4, 5.4-1.6, 1.6-0.7, and < 0.7 μm). Samples collected were chemically analyzed for all the five size ranges, for the estimation of 16 different PAHs. The particle size distribution of PAHs was observed to be unimodal in nature with the highest peak towards the smallest size aerosol particle (< 0.7 μm). The five size ranges were categorized into two broad categories viz. coarse (> 10.9 + 10.9 to 5.4 + 5.4 to 1.6 μm) and fine (1.6 to 0.7 + < 0.7 μm). It was observed that the dominant PAHs found were pyrene, benzo(a)pyrene, benzo(ghi)perylene and benzo(b)fluoranthene for both the coarse and fine fractions. Source apportionment of polycyclic aromatic hydrocarbons (PAHs) has been carried out using principal component analysis method (PCA) in both coarse and fine size modes. The major sources identified in this study, responsible for the elevated concentration of PAHs in Delhi, are vehicular emission and coal combustion. Some contribution from biomass burning was also observed.     

Concentrations, sources, and spatial distribution of individual polycyclic aromatic hydrocarbons (PAHs) in agricultural soils in the Eastern part of the EU: Poland as a case study

Soils from agricultural areas receive unsatisfactory attention as regards the contamination with organic pollutants. To answer those needs the contents of the sixteen individual PAH compounds were determined (GC/MS technique) in agricultural soils in Poland. The samples (n = 216) were collected from the upper layer of arable land in the year 2005. Half of the samples represented typical rural areas, while the rest derived from the territories potentially subjected to the urban/industrial pressure of various intensity. The mean (geometric) content of individual compounds varied from 1 μg kg^− 1 for acenaphtylene to 55 μg kg^− 1 for fluoranthene with the highest contributions (11.6%-12.9%) of phenanthrene, fluoranthene and pyrene. Higher molecular weight PAHs (4 rings) were strongly linked mutually and with the ∑16PAHs. They contributed substantially (73%) to the overall content of PAHs, which implies domination of anthropogenic sources. The calculated molecular indexes suggest that most of those PAHs derive from the combustion of coal, the main energy source in Poland. Simultaneously, the concentrations of lower molecular weight compounds seem to reflect the background, “natural” PAH compounds, which represent mainly atmospherically distributed emission. The division of the samples into groups describing geographical regions and landscape type enabled evaluation of the spatial trends in contamination of soils with PAH compounds. The most pronounced effect of spatial parameters corresponded to PAHs > 4 rings, while lower molecular weight compounds showed more homogeneous concentration through the country.