Identification of particulate matter sources on an hourly time-scale in a wood burning community

Particulate matter (PM) sources at two different sites in a rural town in New Zealand were investigated on an hourly time-scale. Streaker samplers were used to collect hourly, size-segregated PM(10-2.5) and PM(2.5) samples that were analyzed for elemental content using ion beam analysis techniques. Black carbon concentrations were determined using light reflection and PM(10) concentrations were recorded using colocated continuous PM monitors. PM(10) concentrations at both sites displayed a diurnal pattern, with hourly PM(10) concentration maxima in the evening (7 pm-midnight) and in the morning (7-9 am). One of the monitoring sites experienced consistently higher average PM(10) concentrations during every hour and analysis indicated that katabatic flows across the urban area contributed to the increased concentrations observed. Source apportionment using positive matrix factorization on the hourly data revealed four primary PM(10) sources for each site: biomass burning, motor vehicles, marine aerosol and crustal matter. Biomass burning was the most dominant source at both sites and was responsible for both the evening and morning PM(10) concentration peaks. The use of elemental speciation combined with PM(10) concentrations for source apportionment on an hourly time-scale has never been reported and provides unique and useful information on PM sources for air quality management.     

Residual indoor contamination from world trade center rubble fires as indicated by polycyclic aromatic hydrocarbon profiles

The catastrophic destruction of the World Trade Center (WTC) on Sept. 11, 2001 (9/11) created an immense dust cloud followed by fires that emitted smoke and soot into the air of New York City (NYC) well into December. Outdoor pollutant levels in lower Manhattan returned to urban background levels after about 200 days as the fires were put out and the debris cleanup was completed. However, particulate matter (PM) from the original collapse and fires also penetrated into commercial and residential buildings. This has created public concern because WTC dust is thought to cause adverse pulmonary symptoms including "WTC cough" and reduced lung capacity. Additionally, some recent studies have suggested a possible link between exposure to WTC contamination and other adverse health effects. Distinguishing between normal urban pollutant infiltration and residual WTC dust remaining in interior spaces is difficult; efforts are underway to develop such discriminator methods. Some progress has been made in identifying WTC dust by the content of fibers believed to be associated with the initial building collapse. There are also contaminants created by the fires that burned for 100 days in the debris piles of the building rubble. Using WTC ambient air samples, we have developed indicators for fire related PM based on the relative amounts of specific particle bound polycyclic aromatic hydrocarbons (PAHs) and the mass fraction of PAHs per mass of PM. These two parameters are combined, and we show a graphical method for discriminating between fire sources and urban particulate sources as applied to samples of settled dusts. We found that our PAHs based discriminator method can distinguish fire source contributions to WTC related particulate matter and dusts. Other major building fires or large open burn events could have similar PAHs characteristics. We found that random samples collected approximately 3.5 years after the WTC event from occupied indoor spaces (primarily residential) in the New York area are not statistically distinguishable from contemporary city background.     

Tracking petroleum refinery emission events using lanthanum and lanthanides as elemental markers for PM2.5

Fine particulate matter levels at four air sampling stations in the Houston, TX area are apportioned to quantify the impact of emissions from a local refinery during a reported emission event. Through quantification of lanthanum and lanthanides using a recently developed analytical technique, the impacts of emissions from fluidized-bed catalytic cracking (FCC) units are quantitatively tracked across the Houston region. The results show a significant (33-106-fold) increase in contributions of FCC emissions to PM2.5 compared with background levels associated with routine operation. This impact from industrial emissions to ambient air quality occurs simultaneously with a larger, regional haze episode that lead to elevated PM2.5 concentrations throughout the entire region. By focusing on detailed chemical analysis of unique maker metals (lanthanum and lanthanides), the impact of emissions from the FCC unit was tracked from the local refinery that reported the emission event to a site approximately 50 km downwind, illustrating the strength of the analytical method to isolate an important source during a regional haze episode not related to the emission event. While this source apportionment technique could separate contributions from FCC emissions, improved time-resolved sampling is proposed to more precisely quantify the impacts of transient emission events on ambient PM2.5.     

Chemical characteristics of PM2.5 and PM10 in haze-fog episodes in Beijing

Aerosol samples of PM2.5 and PM10 in a period of intensive haze-fog (HF) events were collected to investigate the chemical characteristics of air pollution in Beijing. The air quality in HF episodes was much worse than that in nonhaze-fog (NHF) days. The concentrations of elements and water-soluble (WS) ions (K+, So4(2-), and NO3-) in HF episodes were more than 10 times higher than those in NHF days. Most of the chemical species in PM2.5 and the secondary species (NH4+, So4(2-), and NO3-) in PM10 showed significant difference between HF from westerly direction (HFW) and southerly direction (HFS). The concentrations of secondary species in HFS were much higher than those in HFW, and other chemical species in HFS were lower than those in HFW. The sources of PM2.5 were more from areas on the regional scale due to its tendency for long-range transport, while PM10 was more limited to the local sources. Aerosol particles were more acidic in HFS and more alkaline in HFW. The secondary species were the major chemical components of the aerosol in HF episodes, and their concentrations increased in the order of NHF < HFW < HFS. High concentrations of the secondary aerosol in HF episodes were likely due to the higher sulfur and nitrogen oxidation rate in aqueous-phase reactions. The serious air pollution in HF episodes was strongly correlated with the meteorological conditions and the emissions of pollutants from anthropogenic sources.     

Atmospheric polycyclic aromatic hydrocarbons in north China: a winter-time study

The contamination and outflow of atmospheric polycyclic aromatic hydrocarbons (PAHs) in the Chinese Northern Plain, a region with a total area of 300 000 km2 and a high PAH emission density, were investigated. Polyurethane foam (PUF) and PM10 samples were collected at 46 sites located in urban, rural (towns or villages), and control (remote mountain) areas in the winter from November 2005 to February 2006. The observed concentrations of atmospheric PAHs were generally higher than those reported for developed countries and southern Chinese cities. It was found that there was no significant difference in air PAH concentrations between the urban and the rural areas (514 +/- 563 ng/m3 and 610 +/- 645 ng/ m3, respectively), while the PAH concentrations at the control sites (57.1 +/- 12.6 ng/m3) were 1 order of magnitude lower than those at the other sites. The primary reason for the similarity in PAH concentrations between urban and rural areas was the fact that the predominant sources of biomass and domestic coal combustion were widely spread over the study area. The partition constants (K(PM10)) of PAHs were significantly correlated to the corresponding values of subcooled liquid-vapor pressure (pL0). However, the regression slopes of log K(PM10) versus log pL0 were much steeper than -1, indicating adsorption dominated over absorption. Three distinct patterns of outflow from the study area were identified by forward trajectory and cluster analysis.     

Assessing the performance of methods to detect and quantify African dust in airborne particulates

African dust (AD) contributions to particulate matter (PM) levels may be reported by Member States to the European Commission during justification of exceedances of the daily limit value (DLV). However, the detection and subsequent quantification of the AD contribution to PM levels is complex, and only two measurement-based methods are available in the literature: the Spanish-Portuguese reference method (SPR), and the Tel Aviv University method (TAU). In the present study, both methods were assessed. The SPR method was more conservative in the detection of episodes (71 days identified as AD by SPR, vs 81 by TAU), as it is less affected by interferences with local dust sources. The mean annual contribution of AD was lower with the TAU method than with SPR (2.7 vs 3.5 ± 1.5 μg/m(3)). The SPR and TAU AD time series were correlated with daily aluminum levels (a known tracer of AD), as well as with an AD source identified by the Positive Matrix Factorization (PMF) receptor model. Higher r(2) values were obtained with the SPR method than with TAU in both cases (r(2) = 0.72 vs 0.56, y = 0.05x vs y = 0.06x with aluminum levels; r(2)=0.79 vs 0.43, y = 0.8x vs y = 0.4x with the PMF source). We conclude that the SPR method is more adequate from an EU policy perspective (justification of DLV exceedances) due to the fact that it is more conservative than the TAU method. Based on our results, the TAU method requires adaptation of the thresholds in the algorithm to refine detection of low-impact episodes and avoid misclassification of local events as AD.     

Multisite study of particle number concentrations in urban air

Particle number concentration data are reported from a total of eight urban site locations in the United Kingdom. Of these, six are central urban background sites, while one is an urban street canyon (Marylebone Road) and another is influenced by both a motorway and a steelworks (Port Talbot). The concentrations are generally of a similar order to those reported in the literature, although higher than those in some of the other studies. Highest concentrations are at the Marylebone Road site and lowest are at the Port Talbot site. The central urban background locations lie somewhere between with concentrations typically around 20 000 cm(-3). A seasonal pattern affects all sites, with highest concentrations in the winter months and lowest concentrations in the summer. Data from all sites show a diurnal variation with a morning rush hour peak typical of an anthropogenic pollutant. When the dilution effects of windspeed are accounted for, the data show little directionality at the central urban background sites indicating the influence of sources from all directions as might be expected if the major source were road traffic. At the London Marylebone Road site there is high directionality driven by the air circulation in the street canyon, and at the Port Talbot site different diurnal patterns are seen for particle number count and PM10 influenced by emissions from road traffic (particle number count) and the steelworks (PM10) and local meteorological factors. Hourly particle number concentrations are generally only weakly correlated to NO(x) and PM10, with the former showing a slightly closer relationship. Correlations between daily average particle number count and PM10 were also weak. Episodes of high PM10 concentration in summer typically show low particle number concentrations consistent with transport of accumulation mode secondary aerosol, while winter episodes are frequently associated with high PM10 and particle number count arising from poor dispersion of local primary emissions.     

Levels and isomer profiles of dechlorane plus in Chinese air

The highly chlorinated flame retardant, Dechlorane Plus (DP), was measured in air across 97 Chinese urban and rural sites. DP was detected in 51 of these sites, with a mean air concentration in urban centers (15.6 +/- 15.1 pg m(-3)) approximately 5 times greater than those measured in rural areas (3.5 +/- 5.6 pg m(-3)). These DP levels were likely attributable to local sources rather than trans-boundary influences. Elevated urban levels were measured along the southeastern coast and in south-central China; the highest concentration was observed in the city of Kunming (66 pg m(-3)). Few of the urban samples (7%) and a majority of the rural samples (62%) were below the method detection limit, notably areas in rural central and northeastern China. The mean fractional abundance of the syn-DP isomer (f(syn)) in all samples was 0.33 +/- 0.10, values indistinguishable from that of a commercial mixture (f(syn) = 0.35). This paper represents the first report on DP levels in Chinese air, together with isomeric ratio profiles from urban and rural sites.     

Poly and perfluorinated carboxylates in North American precipitation

Although perfluorocarboxylates (PFCAs) have been detected in a number of environmental matrices, there are very few reports on concentrations in precipitation. In this study PFCAs, fluorotelomercarboxylates (FTCAs), and fluorotelomer-unsaturated carboxylates (FTUCAs), were determined in wet only precipitation samples from nine sites in North America. The analytical method involved derivatization of the carboxylates and measurement of the 2,4-difluoroanilide by GC-MS. Samples from three remote sites in Canada had low concentrations of perfluorooctanoate (PFOA) (<0.1-6.1 ng/L). Significantly higher concentrations of PFOA were found at 4 northeastern United States and 2 southern urban Canadian sites, with Delaware having the highest levels (85 ng/L PFOA, with a range of 0.6-89 ng/L) and a maximum flux of 13 000 ng/m2. 8:2- and 10:2 FTCAs and FTUCAs were detected at all 4 U.S. sites and 2 urban Canadian sites (<0.07-8.6 ng/L), most frequently at the Delaware site. Longer chained PFCAs (deca-, undeca-, and dodeca-perfluorocarboxylates) were detected (<0.07-5.2 ng/L) at 2 urban Ontario sites but not determined in other samples. Air mass back trajectory results for 3 U.S. sites indicate highly populated urban areas in the New York to Washington corridor as the main sources of PFOA, although low PFOA levels associated with air masses coming off the Atlantic Ocean imply multiple sources.     

Analysis of polychlorinated biphenyls in concurrently sampled Chinese air and surface soil

Polychlorinated biphenyl (PCB) concentrations were measured in a concurrent air and surface soil sampling program across China. Passive air samples were collected for approximately 3 months from mid-July to mid-October, 2005 using polyurethane foam (PUF) disk type samplers at 97 sites and surface soil samples were collected in a subset of 51 sites in the same year. As expected, the air concentrations (pg m(-3)) were highest at urban sites (mean of 350 +/- 218) followed by rural (230 +/- 180) and background sites (77 +/- 50). The PCB homologue composition was similar across China, with no distinction among site types, and reflected the profile of Chinese transformer oil with a greater proportion of lower molecular weight (LMW) congeners, particularly the tri-PCBs. This differs from the profile in Chinese soil that was shifted toward the higher molecular weight (HMW) congeners and likely attributed to numerous years of deposition and accumulation in this reservoir. The PCB profile in surface soil also reflects an "urban fractionation effect" with preferential deposition of HMW congeners near sources. The profile of PCBs in Chinese air was shown to be different than reported for Europe and for the Great Lakes Area (GLA) in North America. European and GLA air samples show a distinction between urban and rural/V background sites, with urban sites dominated by tetra- and penta-PCBs, whereas rural and background sites are shifted toward LMW congeners. European and GLA samples also exhibit much higher PCB concentrations at urban sites. This may be attributed to the use of PCBs in building materials in European and North American cities. In China, the difference between urban and rural/background sites is less pronounced. Strong soil-air correlations were found for the LMW PCBs at the background and rural sites, and for the HMW PCBs at the urban sites, a strong evidence of the urban fractionation effect. To our knowledge, this is the first national-scale study in China investigating PCBs in both air and surface soil samples.     

工业废水处理装置中的废气治理技术

废气治理工程是环境工程的一个重要组成部分。废气处理工程的初期主要以锅炉及工业窑炉为控制对象的消烟除尘工作。随后又开展了各类工业企业废气治理工作并在脱硫、除尘、脱硝、汽车尾气等单项废气处理方面取得成效。紧接着,在工业污染源废气处理、城市大气污染防治、区域大气污染控制等方面做出了巨大努力。随着民众对环境质量要求日益提高,解决众多工业污水处理系统中产生的恶臭气体的影响问题也提上议事日程。本文对工业废水处理装置中废气治理技术的应用进行了研究,希望为相关工作的开展,提供借鉴。     

Fine (PM2.5) and coarse (PM2.5-10) particulate matter on a heavily trafficked London highway: sources and processes

A large dataset for PM2.5 and PMcoarse (PM2.5-10) concentrations monitored near a busy London highway (Marylebone Road) has been analyzed to define the factors that lead to high concentrations. The following have been highlighted as major influencing parameters: wind speed, prevailing wind direction (because of its role on the microscale dispersion within the street), the daily cycle of the atmospheric boundary layer (stable during the night/ convective and mixed during the day), and traffic density. The mainly diesel heavy-duty vehicles are the main source of fine particulate matter at Marylebone Road. In particular, lorries (trucks) dominate PM10 exhaust emissions which are mainly in the fine (<2.5 microm) size range. A strong correlation with PMcoarse suggests that the heavy-duty traffic is largely responsible for this component also. Substantial local increments in PM2.5 and PMcoarse due to traffic have been estimated and a large part of the increment in PMcoarse concentrations is inferred to arise from resuspended road dust emissions since the contribution of abrasion processes estimated from emission factors is modest. Despite the strong influence of traffic on PM concentrations measured at Marylebone Road the analysis of factors leading to the highest 5% of hourly concentrations of PM10 at Marylebone Road reveals that almost half of these events were due to building works. The other events occurred when all or most of the key factors occurred simultaneously (heavy traffic, poor dispersion, etc.). Some episodes of high PM2.5 concentrations were associated with long-range transport in which the regional PM2.5 constituted most of the local concentrations.     

A general indication of the Contemporary background levels of PCDDs, PCDFs, and coplanar PCBs in the ambient air over rural and remote areas of the United States

Long-term measurements of the atmospheric concentrations of PCDDs, PCDFs, and coplanar PCBs were taken in rural and remote areas of the United States by the National Dioxin Air Monitoring Network (NDAMN). A total of 21 quarterly sampling moments occurred from June, 1998 to December, 2002 at 34 locations geographically distributed throughout the United States. Sampling sites were located in rural and remote areas to obtain background air concentrations of dioxin-like compounds. Results were reported as the toxic equivalent (TEQ) of the mix of PCDDs/ PCDFs (TEQDF) and the mix of coplanar PCBs (TEQPCB). At the studied rural sites the mean annual TEQDF for each of the NDAMN sampling years was 10.43, 11.39, 10.40, and 10.47 fg m(-3) for 1999, 2000, 2001, and 2002, respectively. There was no statistically significant difference in the rural mean TEQDF air concentrations across the sampling years (at 0.05 level of significance), although the mean concentration in sampling year 2000 increased 10% relative to the other sampling years. The 95th percent confidence interval of TEQDF air concentrations in rural areas of the United States is from 6.4 to 15.4 fg m(-3), indicating there is a 95% probability that the true mean falls within this range. Mean annual atmospheric concentrations (TEQDF) at the remote sites were 1.41, 0.99, 0.7, and 1.07 fg m(-3) in 1999, 2000, 2001, and 2002, respectively, The 95th percent confidence interval of TEQDF air concentrations suggest that the true mean annual atmospheric TEQDF concentration in remote areas of the United States is between 0.1 and 3 fg m(-3). The remote sites have average air TEQDF concentrations that are approximately 10 times lower than those of the rural sites. For the rural sites, there was close agreement in the mean annual air concentrations of coplanar PCBs (TEQPCB) among the years 1999, 2000, 2001, and 2002 (i.e., 0.62, 0.69, 0.59, and 0.7 fg m(-3), respectively). However, as is the case with PCDDs/PCDFs, there was a marked increase (i.e., approximately equal to 13%) in the annual rural mean air concentration in 2000 as compared to the other sampling years. The confidence intervals across the NDAMN sampling years suggests a 95% probability that mean TEQPcB atmospheric concentrations in rural and remote areas of the United States are within the range of 0.5-0.9 fg m(-3) and 0.1-0.5 fg m(-3), respectively. The congener distributional patterns of PCDDs/PCDFs in air were relatively constant at all locations, and match the profile of urban air. We propose the hypothesis that urban areas are regional sources of PCDDs/PCDFs and are affecting atmospheric levels in rural and remote areas of the United States.     

Cloud and fog processing enhanced gas-to-particle partitioning of trimethylamine

An aerosol time-of-flight mass spectrometer (ATOFMS) was used to detect trimethylamine (TMA) in 0.52-1.9 μm particles at urban and rural sites in Southern Ontario during the summer and winter of 2007. During the summer, TMA-containing particles were observed exclusively during high relative humidity or fog events at both the urban and rural sites. In the wintertime, greater concentrations of TMA-containing particles were linked to cloud processing of aerosol in air masses originating from over agricultural and livestock areas. A laboratory study revealed that, at high relative humidity (～ 100%), gas phase TMA at concentrations ranging from 2 to 20,000 ppt partitions preferentially to acidic particles present in the ambient air. On the basis of the field and laboratory studies, it appears that gas phase TMA present in ambient air partitions onto pre-existing particles preferentially during periods of acidic cloud/fog processing, leading to the presence of TMA-containing particles in the 0.52-1.9 μm size range.     

Spatial distribution of polybrominated diphenyl ethers in southern Ontario as measured in indoor and outdoor window organic films

Organic films were collected from indoor and outdoor window surfaces, along an urban-rural transect extending northward from Toronto, Ontario, Canada, and analyzed for 41 polybrominated diphenyl ether congeners (PBDE). For exterior films, urban sigmaPBDE concentrations were approximately 10x greater than rural concentrations, indicating an urban-rural gradient and greater PBDE sources in urban areas. Urban films ranged from 2.5 to 14.5 ng/m2 (mean = 9.0 ng/ m2), excluding the regional "hotspot" Electronics Recycling Facility, compared to 1.1 and 0.56 ng/m2 at the Suburban and Rural sites. Interior urban films (mean = 34.4 ng/m2) were 3 times greater than rural films (10.3 ng/m2) and were representative of variations in building characteristics. Indoor films were 1.5-20 times greater than outdoor films, consistent with indoor sources of PBDEs and enhanced degradation in outdoor films. Congener profiles were dominated by BDE-209 (51.1%), consistent with deca-BDE as the main source mixture, followed by congeners from the penta-BDE mixture (BDE-99:13.6% and -47:9.4%) and some octa-BDE (BDE-183:1.5%). Congener patterns suggest a degradative loss of lower brominated compounds in outdoor films versus indoor films. Gas-phase air concentrations were back-calculated from film concentrations using the film-air partition coefficient (K(FA)). Mean calculated air concentrations were 4.8 pg/m3 for outdoor and 42.1 pg/m3 for indoor urban sites, indicating that urban indoor air is a source of PBDEs to urban outdoor air and the outdoor regional environment.     

Polychlorinated naphthalenes in Great lakes air: assessing spatial trends and combustion inputs using PUF disk passive air samplers

Passive air samplers made from polyurethane foam (PUF) disks housed in stainless steel chambers were deployed over four seasons during 2002-2003, at 15 sites in the Laurentian Great lakes, to assess spatial and temporal trends of polychlorinated naphthalenes (PCNs). Sampling rates, determined using depuration compounds pre-spiked into the PUF disk prior to exposure, were, on average, 2.9 +/- 1.1 m3 d(-1), consistent with previous studies employing these samplers. PCN air concentrations exhibited strong urban-rural differences-typically a few pg m(-3) at rural sites and an order of magnitude higher at urban sites (Toronto, 12-31 pg m(-3) and Chicago,13-52 pg m(-3)). The high concentrations at urban sites were attributed to continued emissions of historically used technical PCN. Contributions from combustion-derived PCNs seemed to be more important at rural locations where congeners 24 and 50, associated with wood and coal burning, were elevated. Congener 66/67, associated with incineration and other industrial thermal processes, was elevated at two sites and explained by nearby and/or upwind sources. Probability density maps were constructed for each site and for every integration period were shown to be a useful complement to seasonally integrated passive sampling data to resolve source-receptor relationship for PCNs and other pollutants.     

Characterization and source apportionment of particulate matter < or = 2.5 micrometer in Sumatra, Indonesia, during a recent peat fire episode

An intensive field study was conducted in Sumatra, Indonesia, during a peat fire episode to investigate the physical and chemical characteristics of particulate emissions in peat smoke and to provide necessary data for source-receptor analyses. Ambient air sampling was carried out at three different sites located at varying distances from the peatfires to determine changes in mass and number concentrations of PM2.5 and its chemical composition (carbonaceous and nitrogenous materials, polycyclic aromatic hydrocarbons, water-soluble inorganic and organic ions, and total and water-soluble metals). The three sites represent a rural site directly affected by the local peat combustion, a semirural site, and an urban site situated downwind of the peat fires. The mass concentration of PM2.5 and the number concentration of airborne particles were as high as 1600 microg/m3 and 1.7 x 10(5) cm(-3), respectively, in the vicinity of peat fires. The major components of PM2.5 in peat smoke haze were carbonaceous particles, particularly organic carbon, NO3-, and SO4(2-), while the less abundant constituents included ions such as NH4+, NO2-, Na+, K+, organic acids, and metals such as Al, Fe, and Ti. Source apportionment by chemical mass balance receptor modeling indicates that peat smoke can travel long distances and significantly affect the air quality at locations downwind.     

Spatial and temporal trends of chiral organochlorine signatures in Great Lakes air using passive air samplers

Passive air samples (PAS) were collected and analyzed to assess the spatial and temporal trends of chiral organochlorine signatures in the Laurentian Great Lakes. Samples were collected from 15 sites and analyzed for the concentrations and enantiomer signature of chlordanes and alpha-hexachlorocyclohexane (alpha-HCH). Levels of the chlordanes were typically 4 times higher in urban areas than what were observed at rural and remote locations, exhibiting strong urban-rural gradients. Near racemic residues were seen for the chlordane enantiomers in samples collected from sites located in Toronto and Chicago, which can be attributed to continued emissions of historical use of the technical chlordane mixture, while the chiral signature observed at sites located in rural and remote locations was indicative of an aged source. Knowledge of the spatial and temporal distribution of the enantiomer signatures of chlordane and alpha-HCH in air is useful for distinguishing sources of these compounds to ambient air. Results suggest that potential sources, such as those associated with Toronto and Chicago, have limited influence over the levels at rural and remote sites within the Great Lakes. Sources that are relatively close to sample sites, however, have a strong influence on levels observed at those sites. For instance, results indicate that Lake Superior continues to act as a source of alpha-HCH to sites located on its shores. Generally, it appears that during the warmer months, local enhanced surface-air exchange influences air concentrations and that during the cooler periods of the year, levels in the atmosphere are more strongly influenced by advective transport from source regions.     

Human-cell mutagens in respirable airborne particles in the northeastern United States. 1. Mutagenicity of fractionated samples

Few studies have characterized the regional scale (300-500 km) variability of the mutagenicity of respirable airborne particles (PM2.5). We previously collected 24-h PM2.5 samples for 1 year from background, suburban, and urban sites in Massachusetts (MA) and rural and urban sites in upstate New York (NY) (n = 53-60 samples per site). Bimonthly composites of these samples were mutagenic to human cells. The present report describes our effort to identify chemical classes responsible for the mutagenicity of the samples, to quantify spatial differences in mutagenicity, and to compare the mutagenicity of samples composited in different ways. Organic extracts and HPLC fractions (two nonpolar, one semipolar, and one polar) of annual composites were tested for mutagenicity in the h1A1v2 cells, a line of human B-lymphoblastoid cells that express cytochrome P450 CYP1A1 cDNA. The mutagenic potency (induced mutant fraction per microg organic carbon) of the semipolarfractions was the highest at all five sites, accounting for 35-82% of total mutagenic potency of the samples, vs the nonpolar (4-38%) and polar (14-32%) fractions. These results are consistent with previous studies. While unfractionated extracts exhibited no spatial variations, the mutagenicity of semipolar fractions at the NY sites was approximately 2-fold higher than at the MA sites. This suggests there may be significant regional differences in the sources and/ or transport and transformation of mutagenic compounds in PM2.5. In addition, mutagenic potency was sensitive to whether samples were fractionated and how they were composited: unfractionated annual composite samples at the NY sites were significantly less mutagenic than their semipolar fractions and the annual average of bimonthly composites; spatial differences in the mutagenic potency of bimonthly composites and the semipolar fractions were not apparent in the annual composites.     

Primary sources and secondary formation of organic aerosols in beijing, china

Ambient aerosol samples were collected at an urban site and an upwind rural site of Beijing during the CAREBEIJING-2008 (Campaigns of Air quality REsearch in BEIJING and surrounding region) summer field campaign. Contributions of primary particles and secondary organic aerosols (SOA) were estimated by chemical mass balance (CMB) modeling and tracer-yield method. The apportioned primary and secondary sources explain 73.8% ± 9.7% and 79.6% ± 10.1% of the measured OC at the urban and rural sites, respectively. Secondary organic carbon (SOC) contributes to 32.5 ± 15.9% of the organic carbon (OC) at the urban site, with 17.4 ± 7.6% from toluene, 9.7 ± 5.4% from isoprene, 5.1 ± 2.0% from α-pinene, and 2.3 ± 1.7% from β-caryophyllene. At the rural site, the secondary sources are responsible for 38.4 ± 14.4% of the OC, with the contributions of 17.3 ± 6.9%, 13.9 ± 9.1%, 5.6 ± 1.9%, and 1.7 ± 1.0% from toluene, isoprene, α-pinene, and β-caryophyllene, respectively. Compared with other regions in the world, SOA in Beijing is less aged, but the concentrations are much higher; between the sites, SOA is more aged and affected by regional transport at the urban site. The high SOA loading in Beijing is probably attributed to the high regional SOC background (～2 μg m(-3)). The toluene SOC concentration is high and comparable at the two sites, implying that some anthropogenic components, at least toluene SOA, are widespread in Beijing and represents a major factor in affecting the regional air quality. The aerosol gaseous precursor concentrations and temperature correlate well with SOA, both affecting SOA formation. The significant SOA enhancement with increasing water uptake and acidification indicates that the aqueous-phase reactions are largely responsible SOA formation in Beijing.