Size-segregated characteristics of water-soluble oxidative potential in urban Xiamen: Potential driving factors and implications for human health.

Oxidative potential (OP), defined as the ability of particulate matter (PM) to generate reactive oxygen species (ROS), has been considered as a potential health-related metric for PM. Particles with different sizes have different OP and deposition efficiencies in the respiratory tract and pose different health risks. In this study, size-segregated PM samples were collected at a coastal urban site in Xiamen, a port city in southeastern China, between August 2020 and September 2021. The water-soluble constituents, including inorganic ions, elements and organic carbon, were determined. Total volume-normalized OP based on the dithiothreitol assay was highest in spring (0.241 ± 0.033 nmol min-1 m-3) and lowest in summer (0.073 ± 0.006 nmol min-1 m-3). OP had a biomodal distribution with peaks at 0.25-0.44 µm and 1.0-1.4 µm in spring, summer, and winter and a unimodal pattern with peak at 0.25-0.44 µm in fall, which were different from the patterns of redox-active species. Variations in the seasonality of fine and coarse mode OP and their correlations with water-soluble constituents showed that the size distribution patterns of OP could be attributed to the combined effects of the size distributions of transition metals and redox-active organics and the interactions between them which varied with emissions, meteorological conditions and atmospheric processes. Respiratory tract deposition model indicated that the deposited OP and the toxic elements accounted for 47.9 % and 36.8 % of their measured concentrations, respectively. The highest OP doses and the excess lifetime carcinogenic risk (ELCR) were found in the head airway (>70 %). However, the size distributions of OP deposition and ELCR in the respiratory tract were different, with 63.9 % and 49.4 % of deposited ELCR and OP, respectively, coming from PM2.5. Therefore, attention must be paid to coarse particles from non-exhaust emissions and road dust resuspension.

[Atmospheric NH3 Emission Inventory and Its Tempo-spatial Changes in Xiamen-Zhangzhou-Quanzhou Region from 2015 to 2020].

Based on the district and county activity level data of different types of atmospheric ammonia (NH3) emission sources in the Xiamen-Zhangzhou-Quanzhou (XZQ) Region and the modified emission factors, an ammonia emission inventory with a spatial resolution of 1 km×1 km in 2017 was established. In addition, the annual variations in NH3 emission from 2015 to 2020 in this region were analyzed. The results showed that the emission of NH3 in the XZQ Region in 2017 was 27.40 kt with livestock and poultry breeding, farmland ecosystem, human emission, fuel combustion, and waste treatment accounting for 42.48%, 22.04%, 14.71%, 7.08%, and 5.69% of the total emission, respectively. The order of emission density of NH3 was Xiamen (1.94 t·km-2)>Quanzhou (1.07 t·km-2)>Zhangzhou (0.95 t·km-2). High values of emission density were mainly concentrated in the coastal urban areas with a concentrated population and the inland township areas with developed livestock and poultry breeding and planting industries. The monthly variation in NH3 emissions was consistent with the pattern of temperature change, with high values in summer. Due to the different economic structure and development level in different cities, NH3 emissions in Quanzhou City showed a decline from 2015 to 2020, whereas there were fluctuations in the trends of ammonia emissions in Xiamen and Zhangzhou cities. The relationship between NH3 emission intensity and per capita GDP was significantly negative.

[Characterization and Health Risk Assessment of Heavy Metals in PM2.5 in Xiamen Port].

PM2.5 samples at Haitian and Songyu container terminals in Xiamen Port were collected in summer and autumn/winter in 2020 and analyzed for 20 elements to investigate their temporal-spatial distribution features, sources, and health risk. The results showed that the levels of PM2.5 were relatively low and did not show significant spatial and diurnal differences. Ca and Si were the main crustal elements, and Zn and Mn were the main heavy metals in PM2.5. Compared with GB 3095-2012 guidelines, Cr(Ⅵ) was in the range of 27.4-28.6 times above the standard. Under the influence of monsoon and port throughput, the concentrations of some elements in summer were higher than those in autumn/winter. Significant diurnal variations were observed for Cu, Zn, SO2, and NO2 but not for V and Ni. Industrial sources were identified as the primary contributor (55.2%-59.4%), followed by traffic (28.7%-31.3%), ship emissions (7.1%-7.7%), and sea salt plus construction dust (4.8%-5.8%). The results of health risk assessment showed that heavy metals in PM2.5in Xiamen Port had potential carcinogenic risk (ECR>1(10-5) to people living near the port, and Cr(Ⅵ), V, and As together accounted for 97.3%-97.5% of the total risks; however, the non-carcinogenic risk was negligible (HI<1), and the major contributors were V, Mn, Ni, and As (89.6%-91.2%). The relative contributions of each contributor to ECR was in the order of traffic (47.2%-49.4%)>industrial (23.8%-24.2%)>ship emissions (16.9%-20.8%)>sea salt plus construction dust (5.7%-12.1%), and the relative contribution to HI was in the order of traffic (38.7%-42.3%)>industrial (24.5%-28.2%)>ship emissions (24.1%-27.2%)>sea salt plus construction dust (5.4%-9.6%).

Solubility of aerosol minor and trace elements in Xiamen Island, Southeast China: Size distribution, health risk and dry deposition.

Aerosol element solubility is essential to evaluate the damage to the environment and human health. In this work, the size distribution of total and soluble elements in eight particle size ranges with diameter <0.25, 0.25-0.44, 0.44-1.0, 1.0-1.4, 1.4-2.5, 2.5-10, 10-16 and >16 µm was investigated in Xiamen Island, southeast China from March 2018 to June 2020. The results showed that both total and soluble elements exhibited significant size dependence without obvious seasonal variations, and their relative contributions to PM1 mass were much lower than in particles larger than 1 µm. The correlations between some elements in soluble fraction were quite different from those in total fraction and the correlations also varied with particle size due to their different solubility. The solubility of Al, Fe, Ag and Cr was relatively low compared with other elements. Moreover, the solubility of Na, Mg, Ca, Mn and Ag was less dependent on particle size while Al, Fe and other trace elements exhibited the highest solubility in PM1 and the lowest in PM>10. Overall, the solubility of elements is primarily a function of aerosol origin and size. The carcinogenic risks of metal exposure via inhalation for children (3.31 × 10-6) and adults (4.42 × 10-6) were slightly higher than the guideline of cancer risk with >60 % from V. As for non-carcinogenic risk, the hazard index values for children and adults were 1.59 and 0.53, respectively, with Mn, V and Ni together accounting for >85 % of the risk. >85 % of the size-dependent dry deposition fluxes of the selected soluble elements over the Xiamen Bay were contributed by particles larger than 10 µm due to their high deposition velocities. The atmospheric inputs of bioavailable Fe and Cu to the sea exceeded the required amounts relative to inorganic nitrogen to meet the growth of phytoplankton.

Size distributions and dry deposition fluxes of water-soluble inorganic nitrogen in atmospheric aerosols in Xiamen Bay, China.

Size-segregated aerosol particles were collected using a high volume MOUDI sampler at a coastal urban site in Xiamen Bay, China, from March 2018 to June 2020 to examine the seasonal characteristics of aerosol and water-soluble inorganic ions (WSIIs) and the dry deposition of nitrogen species. During the study period, the annual average concentrations of PM1, PM2.5, PM10, and TSP were 14.8 ± 5.6, 21.1 ± 9.0, 35.4 ± 14.2 µg m-3, and 45.2 ± 21.3 µg m-3, respectively. The seasonal variations of aerosol concentrations were impacted by the monsoon with the lowest value in summer and the higher values in other seasons. For WSIIs, the annual average concentrations were 6.3 ± 3.3, 2.1 ± 1.2, 3.3 ± 1.5, and 1.6 ± 0.8 µg m-3 in PM1, PM1-2.5, PM2.5-10, and PM>10, respectively. In addition, pronounced seasonal variations of WSIIs in PM1 and PM1-2.5 were observed, with the highest concentration in spring-winter and the lowest in summer. The size distribution showed that SO4 2-, NH4 + and K+ were consistently present in the submicron particles while Ca2+, Mg2+, Na+ and Cl- mainly accumulated in the size range of 2.5-10 µm, reflecting their different dominant sources. In spring, fall and winter, a bimodal distribution of NO3 - was observed with one peak at 2.5-10 µm and another peak at 0.44-1 µm. In summer, however, the fine mode peak disappeared, likely due to the unfavorable conditions for the formation of NH4NO3. For NH4 + and SO4 2-, their dominant peak at 0.25-0.44 µm in summer and fall shifted to 0.44-1 µm in spring and winter. Although the concentration of NO3-N was lower than NH4-N, the dry deposition flux of NO3-N (35.77 ± 24.49 µmol N m-2 d-1) was much higher than that of NH4-N (10.95 ± 11.89 µmol N m-2 d-1), mainly due to the larger deposition velocities of NO3-N. The contribution of sea-salt particles to the total particulate inorganic N deposition was estimated to be 23.9-52.8%. Dry deposition of particulate inorganic N accounted for 0.95% of other terrestrial N influxes. The annual total N deposition can create a new productivity of 3.55 mgC m-2 d-1, accounting for 1.3-4.7% of the primary productivity in Xiamen Bay. In light of these results, atmospheric N deposition could have a significant influence on biogeochemistry cycle of nutrients with respect to projected increase of anthropogenic emissions from mobile sources in coastal region. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10874-021-09427-8.

[Response of Air Quality to COVID-19 Lockdown in Xiamen Bay].

Air pollutant concentrations in the Xiamen Bay cities during the period before and after COVID-19 lockdown(from January 11 to February 21, 2020) were studied to determine the influence of human activities on air quality in this region. During the Chinese Spring Festival holiday and the lockdown period, the concentrations of SO2, NO2, CO, PM10, and PM2.5 decreased by 6%-22%, 53%-70%, 34%-48%, 47%-64%, and 53%-60%, respectively. However, the changes in O3 concentrations were not consistent with the variations of human activities. The reduction rates for PM2.5, PM10, CO, and NO2 during the Spring Festival were greater than in previous years(2018 and 2019), but the reduction rates for SO2 were comparable. The concentrations of NO2 increased sharply(38%-138%), and much higher those of SO2(2%-42%), after the resumption of socioeconomic activities, indicating the importance of traffic reductions due to the lockdown measures on NO2. Higher wind speeds and rainfall after the Spring Festival were also favorable for the decline of SO2, NO2, and PM. The spatio-temporal distributions of the six criterial pollutants in the Xiamen Bay city cluster were obtained based on the Inverse Distance Weight method. The variability in regions with high NO2 concentrations was strongly linked to traffic emissions, while spatial patterns for CO and SO2 changed little over the six-week study period. The concentrations of PM2.5 and PM10 increased notably in the region, linked to more construction activity, but changed comparatively little in regions with dense populations and traffic networks. O3 remained relatively stable but low-value regions corresponded to those regions with high NO2 concentrations, indicating the significant titration effect of NO2 on O3. These results provide valuable information that can inform O3 pollution reduction measures.

Size distributions and health risks of particle-bound toxic elements in the southeast coastland of China.

Size-fractionated samples were collected at five coastal urban sites in Fujian Province, southeast China, in 2016 and 2017 to determine the trace elements using ICP-MS. Ca, Fe, Al, Mg, and K were the most abundant elements among the studied elements in TSP, much higher than those of heavy metals. The annual mean concentrations of Pb, As, V, Ni, Cd, and Mn were within the acceptable limits of the World Health Organization and the Ministry of Ecology and Environment of China while Cr(VI) exceeded the limits. Most elements exhibited clear seasonal patterns with maxima over the cold season and minima over the warm season. The spatial variabilities in concentrations of the measured elements were not significant except Ni and V. However, the size distribution pattern of each element was quite similar across the region. Characteristic size distributions of elements allowed identification of three main groups: (a) unimodal distribution in the coarse fraction for Ca, Al, Mg, and Ba; (b) unimodal distribution in the fine fraction for Pb, Se, As, Ag, V, Ni, Zn, and Cd; and (c) bimodal or multimodal distribution for Fe, Mn, Cr, K, and Cu. The combination of the size-fractionated concentrations, enrichment factors, correlation coefficients, and factor analysis offered the identification of mixed sources such as vehicular exhaust and wear, heavy fuel oil combustion, and resuspension of road dust. Non-carcinogenic health risks associated with inhalable exposure to airborne metals were higher than the safety threshold (hazard index > 1) across the region, suggesting non-carcinogenic health risks via inhalation. Mn, V, and Ni contributed 74-83% of the total non-carcinogenic risk. The assessment investigation of carcinogenic health risks revealed V and Cr(VI) as elements with the largest carcinogenic risks, accounting for more than 95% of the overall inhalation risk. Nevertheless, the carcinogenic risks for children and adults were between 10-6 and 10-4, within the range considered acceptable by the US EPA. In terms of the size-fractionated risk, PM2.5 contributed 43-50% and 39-44% of the total non-carcinogenic and carcinogenic risks, respectively, indicating the potential health hazard of coarse particle-bound toxic metals was not negligible.

Nitrogen isotope composition of ammonium in PM2.5 in the Xiamen, China: impact of non-agricultural ammonia.

Since NH3 is a significant precursor to ammonium in PM2.5 and contributes significantly to atmospheric nitrogen deposition but largely remains unregulated in China, the insight into the source of NH3 emissions by the isotopic investigation is important in controlling NH3 emissions. In this study, atmospheric concentrations of NH3 and water-soluble ion composition in PM2.5 as well as nitrogen isotope ratios in NH4+ (δ15N-NH4+) in Xiamen, China, were measured. Results showed that average NH3 concentration for the five sites in Xiamen was 7.9 µg m-3 with distinct higher values in the warm season and lower values in the cold season, and PM2.5 concentration for the two sites (urban and suburban) was 59.2 µg m-3 with lowest values in summer. In the PM2.5, NH4+ concentrations were much lower than NH3 and showed a stronger positive correlation with NO3- than that with SO42- suggesting the formation of NH4NO3 and equilibrium between NH3 and NH4+. Although the concentrations of NH3 at the urban site were significantly higher than those at the suburban site, no significant spatial difference in NH4+ and δ15N-NH4+ was obtained. The distinct heavier δ15N-NH4+ values in summer than in other seasons correlated well with the equilibrium isotopic effects between NH3 and NH4+ which depend on temperature. The initial δ15N-NH3 values were in the range of waste treatment (- 25.42‰) and fossil fuel combustion (- 2.5‰) after accounting for the isotope fractionation. The stable isotope mixing model showed that fossil fuel-related NH3 emissions (fossil fuel combustion and NH3 slip) contributed more than 70% to aerosol NH4+. This finding suggested that the reduction of NH3 emissions from urban transportation and coal combustion should be a priority in the abatement of PM2.5 pollution in Xiamen.

Chemical characteristics, source apportionment, and regional transport of marine fine particles toward offshore islands near the coastline of northwestern Taiwan Strait.

This study aims to investigate the spatiotemporal variation, chemical composition, and source apportionment of marine fine particles (PM2.5) as well as their regional transport toward the Matsu Islands located near the coastline of northwestern Taiwan Strait. Four offshore island sites located at the Matsu Islands were selected to conduct both regular and intensive sampling of marine PM2.5. Water-soluble ionic species, metallic elements, and carbonaceous contents were then analyzed to characterize the chemical characteristics of marine PM2.5. In order to identify the potential sources and their contributions to marine PM2.5, chemical mass balance (CMB) receptor model was employed along with the backward trajectory simulation to resolve the source apportionment of marine PM2.5 and to explore their transport routes in different seasons. The results showed that high PM2.5 concentrations were commonly observed during the northeastern monsoon periods. Additionally, marine PM2.5 concentration decreased from the west to the east with the highest PM2.5 at the Nankang Island and the lowest PM2.5 at the Donyin Island in all seasons, indicating an obvious concentration gradient of PM2.5 transported from the continental areas to the offshore islands. In terms of chemical characteristics of PM2.5, the most abundant water-soluble ions of PM2.5 were secondary inorganic aerosols (SO42-, NO3-, and NH4+) which accounted for 55-81% of water-soluble ions and 29-52% of marine PM2.5. The neutralization ratios of PM2.5 were always less than unity, indicating that NH4+ cannot solely neutralize nss-SO42+ and NO3- in marine PM2.5 at the Matsu Islands. Although crustal elements (Al, Ca, Fe, K, and Mg) dominated the metallic content of marine PM2.5, trace anthropogenic metals (Cd, As, Ni, and Cr) increased significantly during the northeastern monsoon periods, particularly in winter. Organic carbons (OCs) were always higher than elemental carbons (ECs), and the mass ratios of OC and EC were generally higher than 2.2 in all seasons, implying that PM2.5 was likely to be aged particles. During the poor air quality periods, major air mass transport routes were the northern transport and the anti-cyclonic circulation routes. Source apportionment results indicated that fugitive soil dusts and secondary aerosols were the major sources of marine PM2.5 at the Matsu Islands, while, in winter, biomass burning contributed up to 15% of marine PM2.5. This study revealed that cross-boundary transport accounted for 66~84% of PM2.5 at the Matsu Islands, suggesting that marine PM2.5 at the Matsu Islands has been highly influenced by anthropogenic emissions from neighboring Fuzhou City as well as long-range transport from Northeast Asia.

[Seasonal Variations in PM10 and Associated Chemical Species in Jiuxian Mountain in Fujian Province].

PM10 samples were collected at the top of Jiuxian Mountain in Fujian Province from March 2011 to January 2012 and were analyzed for inorganic water-soluble ions and dicarboxylic acids to investigate their seasonal variations and sources. The results showed that PM10 and its associated species exhibited much higher levels in the spring than those in other seasons but the total contribution of the nine species of dicarboxylic acids to PM10 (0.51%±0.41%) was significantly lower than that of the water-soluble ions (18.07%±8.73%). The water-soluble ions were characterized by the highest concentrations of SO42- and NO3-, followed by Na+ and NH4+. Significant positive correlations were observed between cation and anion equivalents, as well as between NH4+ and SO42- or NO3- equivalents. Individual dicarboxylic acid showed a monotonically decreasing trend with increasing carbon number in which oxalic acid accounted for approximately 75% of the total dicarboxylic acids. Characteristic ratios of malonic acid to succinic acid and adipic acid to azelaic acid, MODIS fire spots, and backward trajectories showed that dicarboxylic acids mainly originated from secondary reactions in the atmosphere and that the direct contributions of open biomass burning to dicarboxylic acid concentrations were negligible.

Inter-comparison of Seasonal Variation, Chemical Characteristics, and Source Identification of Atmospheric Fine Particles on Both Sides of the Taiwan Strait.

The spatiotemporal distribution and chemical composition of atmospheric fine particles in areas around the Taiwan Strait were firstly investigated. Fine particles (PM2.5) were simultaneously collected at two sites on the west-side, one site at an offshore island, and three sites on the east-side of the Taiwan Strait in 2013-2014. Field sampling results indicated that the average PM2.5 concentrations at the west-side sampling sites were generally higher than those at the east-side sampling sites. In terms of chemical composition, the most abundant water-soluble ionic species of PM2.5 were SO4(2-), NO3(-), and NH4(+), while natural crustal elements dominated the metallic content of PM2.5, and the most abundant anthropogenic metals of PM2.5 were Pb, Ni and Zn. Moreover, high OC/EC ratios of PM2.5 were commonly observed at the west-side sampling sites, which are located at the downwind of major stationary sources. Results from CMB receptor modeling showed that the major sources of PM2.5 were anthropogenic sources and secondary aerosols at the both sides, and natural sources dominated PM2.5 at the offshore site. A consistent decrease of secondary sulfate and nitrate contribution to PM2.5 suggested the transportation of aged particles from the west-side to the east-side of the Taiwan Strait.

[Simulation Study of the Emission of Polycyclic Aromatic Hydrocarbons and Sugar Alcohols from Biomass Burning].

To measure the emission factors of PM2.5 and its associated PAHs and sugar alcohols, Chinese red pine stick and four crop straw including rice, wheat, corn and cotton were burned in a chamber. In addition, the kinetics of certain compounds were obtained through the irradiation of the glass filters with PM2.5 loading by 500 W mercury lamp. The emission factors of PM2.5 were ranged from (2.26 ± 0.60) g x kg(-1) (Chinese red pine stick) to (14.33 ± 5.26) g x kg(-1) (corn straw). Although the emission factors of the total 19 PAHs differed from (0.82 ± 0.21) mg x kg(-1) (Chinese red pine stick) to (11.14 ± 5.69) mg x kg(-1) (cotton straw), 4 ring PAHs showed predominance over other PAHs accounting for 51% - 71% except Chinese red pine in which retene was the predominant compound. The emission factors of 9 sugar alcohols were ranged from (52.34 ± 50.16) mg x kg(-1) (rice straw) to (238.81 ± 33.62) mg x kg(-1) (wheat straw) with levoglucosan accounting for 72% - 96% of the total sugar alcohols. Both the selected PAHs and levoglucosan associated with PM2.5 followed the first order kinetics. The photolysis kinetic coefficient of PAHs (ring number ≥ 4) was decreased with the increase of PAHs loading in filters. Two PAHs source characteristic ratios such as Flua/( Flua + Py) and IP/(IP + BgP) were relative stable during the irradiation. The photolysis kinetic coefficient of levoglucosan (0.004 5 min(-1)) was comparable to benzo[a]anthracene (0.004 1 - 0.005 0 min(-1)).

[Size distribution of particle and polycyclic aromatic hydrocarbons in particle emissions from simulated emission sources].

Particles from cooking lampblack, biomass and plastics burning smoke, gasoline vehicular exhausts and gasoline generator exhausts were prepared in a resuspension test chamber and collected using a cascade MOUDI impactor. A total of 18 polycyclic aromatic hydrocarbons (PAHs) associated with particles were analyzed by GC-MS. The results showed that there were two peaks in the range of 0.44-1.0 microm and 2.5-10 microm for cooking lampblack, and only one peak in the range of 0.44-1.0 microm for straw and wood burning smoke. But there were no clear peak for plastics burning smoke. The peak for gasoline vehicular exhausts was found in the range of 2.5-10 microm due to the influence of water vapor associated with particles, while the particles from gasoline generator exhausts were mainly in the range of < or = 2.5 microm (accounting for 93% of the total mass). The peak in 2.5-10 microm was clear for cooking lampblack and gasoline vehicular exhausts. The peak in the range of 0.44-1.0 microm became more and more apparent with the increase of PAHs molecular weight. The fraction of PAH on particles less than 1.0 microm to that on the total particles increased along with PAH's molecular weight. Phenanthrene was the dominant compound for cooking lampblack and combustion smoke, while gasoline vehicular exhausts and generator exhausts were characterized with significantly high levels of naphthalene and benzo[g, h, i] perylene, respectively. The distribution of source characteristic ratios indicated that PAHs from cooking lampblack and biomass burning were close and they were different from those of vehicular exhausts and generator exhausts.

[Road dust loading and chemical composition at major cities in Fujian Province].

A total of 57 road dust and 16 urban soil samples were collected from four cities, Xiamen, Zhangzhou, Quanzhou and Putian in Fujian Province, China. Twenty-six elements, eight water soluble ions, organic carbon and elemental carbon in the fraction of particulate diameter less than 2.5 microm (PM2.5) derived through a suspension chamber were analyzed. The average loading of road dust with diameter less than 100 microm in the four cities ranged from 6.99 g x m(-2) to 10.11 g x m(-2), while the loading of PM2.5 ranged from 4.0 mg x m(-2) to 12.5 mg x m(-2). Both the soil and road dust samples were characterized with much higher concentrations of Si, Ca, Al, Fe and K. But for the anthropogenic elements such as Cu, Pb, Zn,Cr and Ti, much lower levels were found in the soil PM2.5, than those in the road dust PM2.5. Significantly higher levels of NH4+, NO3- and SO4(2-) were found in the road dust PM2.5 from Zhangzhou in comparison with those from other cities in this study. The calcium ion (Ca2+) content was significantly positively correlated with the Mg2+ content in the road dust PM2.5 from Xiamen, Zhangzhou and Quanzhou. The levels of organic carbon (OC) in the road dust PM2.5 in these four cities were higher than those reported in Ji'nan, Shijiazhuang and Beijing while the levels of elemental carbon (EC) were all lower than those in the urban road dust from Beijing, Significant positive correlation between EC and OC was found in samples from Quanzhou and Putian, suggesting the same and/or similar sources. The result of mass balance indicated that higher percentage compositions were soil and OM in both Quanzhou and Putian. Based on the cluster analysis, the 57 road dust samples were divided into four types: influenced by atmospheric deposition, influenced by soil dust, influenced by atmospheric deposition and soil dust, and influenced by soil and construction dust.

[Compositions of organic acids in PM10 emission sources in Xiamen urban atmosphere].

The possible organic acid emission sources in PM10 in Xiamen urban atmosphere such as cooking, biomass burning, vehicle exhaust and soil/dust were obtained using a re-suspension test chamber. A total of 15 organic acids including dicarboxylic acids, fatty acids and aromatic acids were determined using GC/MS after derivatization with BF3/n-butanol. The results showed that the highest total concentration of 15 organic acids (53%) was found in cooking emission and the average concentration of the sum of linoleic acid and oleic acid was 24% +/- 14%. However, oxalic acid was the most abundant species followed by phthalic acid in gasoline vehicle exhaust. The ratios of adipic to azelaic acid in gasoline combustion emissions were significantly higher than those in other emission sources, which can be used to qualitatively differentiate anthropogenic and biological source of dicarboxylic acids in atmospheric samples. The ratios of malonic to succinic acid in source emissions (except gasoline generator emissions) were lower (0.07-0.44) than ambient PM10 samples (0.61-3.93), which can be used to qualitatively differentiate the primary source and the secondary source of dicarboxylic acids in urban PM10.

[Characteristics and sources of PM10-bound PAHs during haze period in winter-spring of Xiamen].

PM10 samples were collected at Huli (industrial zone) and Dadeng Island in Xiamen from December 2008 to March 2009. Nineteen polycyclic aromatic hydrocarbons (PAHs) during haze and non-haze periods were determined by GC/MS. Combined with the meteorological data, the differences of chemical composition and source of PAHs were compared. During sampling periods, the concentrations of PM10-bound PAHs ranged from 12.93 to 79.27 ng x m(-3) with the average of 42.28 ng x m(-3), which were almost three times higher than those in the winter of 2004. PAHs concentrations were much higher during the haze periods than those in the non-haze periods. Meanwhile, during the haze periods the percentages of lower molecular weight PAHs such as Phe, Fluo and Pyr decreased significantly, on the contrary, individual components of BbF, BkF, BaP, Per, Icdp, BghiP and COR were more abundant. The main sources of PAHs were estimated by the Principal Component Analysis method and the contributions of various pollution sources to PAHs were calculated by the Multiple Linear Regression method. Results showed that the main pollutant sources of PM10-bound PAHs in winter-spring of Xiamen during the haze period were vehicle emission plus natural gas, coal combustion and coke oven, their contribution rates were 62.7%, 28.1% and 9.2%, respectively. During non-haze periods, the main pollutant sources identified were the same and the contribution rates were 48.6%, 36.9% and 14.5%, respectively. In winter-spring of Xiamen, PM10-bound PAHs were more influenced by local emission sources during the haze periods; coal combustion emissions in north China had a big contribution to PAHs during the non-haze periods.

Seasonal variation for the ratio of BaP to BeP at different sites in Great Xiamen Bay.

From March 2008 to February 2009, PM(10) samples were collected and analyzed for polycyclic aromatic hydrocarbons (PAHs) at eight sampling sites in Great Xiamen Bay, China. Analyses of the seasonal and spatial variations of these compounds revealed the following results. Significantly high levels of PAHs were found in the winter compared to the summer, sometimes exceeding 100 ng m(-3), and the spatial variations were influenced most by the sampling site surroundings. Composition profiles of PAHs of an urban and a rural site were shown to be very similar with a positive correlation coefficient larger than 0.9 at the 0.01 level of significance for the same season. Diagnostic ratios, together with principal component and multiple linear regression analysis, showed that more PAHs were from grass/wood/coal combustion in winter than in other seasons. The ratios of benzo[a]pyrene to benzo[e]pyrene (BaP-BeP) in winter and fall were 0.6-1.7 times higher than those in spring and summer, suggesting the importance of local emissions of PAHs. The BaP-BeP ratios in Kinmen were generally lower than those in Xiamen, indicating that the aging degree of PAHs was higher in Kinmen than in Xiamen. The external input of PAHs from upwind urban and industrial areas was one of the key factors causing high levels of PAHs in PM(10) in Great Xiamen Bay in winter.

[Uncertainty analysis of gas/particle partitioning of atmospheric polycyclic aromatic hydrocarbons].

During the period from August 10, 2010 through August 14, 2010, particle and gas phase PAHs were collected and analyzed using double filters plus PUFs (Poly Urethane Foam) sampling system, and the uncertainties of gas/particle partitioning coefficients of PAHs were investigated using the propagation of errors formulas. The results showed that low-molecular weight PAHs such as naphthalene, acenaphthylene, acenaphthene and fluorene possessed the strong breakthrough capacity with the breakthrough rates close to 50% in double PUF cartridges. The corrected K(p) values based on the sorption of PAHs to the primary filter were more than an order of magnitude higher than those without sorption correction for naphthalene, acenaphthylene and acenaphthene. The uncertainties for all the 19 PAHs ranged from 28.14% to 50.37% based on the standard error propagation formulas, with higher values for volatile and involatile PAHs and lower values for semi-volatile PAHs. The results also showed that the uncertainties of K(p) were mainly contributed from the measurements of particle (average variance contribution was 77.9%) and gas (average variance contribution was 22.0%) phase PAHs while the contributions of total suspended particle were ignorable. Thus, getting more accurate data for gaseous PAHs using an appropriate sampling system is the key to increase the accuracy of gas/particle partitioning coefficients of PAHs.

[Characteristics of PCBs in a capacitor storage site and an industrial brownfield].

The levels and congener patterns of 28 PCBs compounds were investigated in soil and dust fallout collected in a capacitor storage site and an industrial brownfield, respectively in Sichuan Ziyang Locomotive Factory. The highest concentration of the total PCBs(sigma PCBs =227 502 ng x g(-1)) was found in soil collected from the front gate (unsealed) of the capacitor storage tunnel. Very high levels of sigma PCBs, exceed 10 microg x g(-1), were also found in the dust collected from the window sill of an iron foundry. There were significant positive correlations (P < 0.01) among PCB congener concentration in the storage site and the iron foundry samples. The major contribution to the total content of PCBs in the high contaminated samples was tetrachlorinated biphenyls, followed by tri- and penta-chlorinated biphenyls. Hexa- and higher chlorinated biphenyls contributed more to sigma PCBs in the iron foundry than those in the storage site. The total toxicity equivalents (TEQ) of 12 dioxin-like congeners varied in the range of 75.43-24 027 pg x g(-1) and were much higher than those in soils of e-waste recycling sites. However, PCB126 contribute the most to the TEQ in most cases.

[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.