The toxicity of atmospheric fine particulate matter (PM2.5) in Atlanta is assessed using freshwater rotifers (Brachionus calyciflorus). The PM-laden quartz filters were extracted in both water and methanol. Aerosol extracts were passed through a C-18 column to separate the PM components into hydrophobic and hydrophilic fractions. Toxicity data reported in the units of LC50 (concentration that kills 50% of the test population in 24 h) shows that ambient particles are toxic to the rotifers with LC50 values ranging from 5 to 400 μg of PM. The methanol extract of the aerosols was substantially more toxic (8 ± 6 times) to the rotifers compared to the water extracts. A sizeable fraction (>70%) of toxicity was found to be associated with the hydrophobic fraction of PM. However, none of the bulk aerosol species was strongly correlated with the LC50 values suggesting a complicated mechanism of toxicity probably involving synergistic interactions of various PM components.

Four organophosphorus esters (OPEs) were detected in aerosol samples collected in the West Pacific, the Indian Ocean and the Southern Ocean from 2009 to 2010, suggesting their circumpolar and global distribution. In general, the highest concentrations were detected near populated regions in China, Australia and New Zealand. OPE concentrations in the Southern Ocean were about two orders of magnitude lower than those near major continents. Additionally, relatively high OPE concentrations were detected at the Antarctic Peninsula, where several scientific survey stations are located. The four OPEs investigated here are significantly correlated with each other, suggesting they may derive from the same source. In the circumpolar transect, OPE concentrations were associated with ocean gyres in the open ocean. Their concentrations were positively related with average vorticity in the sampling area suggesting that a major source of OPEs may be found in ocean gyres where plastic debris is known to accumulate.

Satellite observations may improve the areal coverage of particulate matter (PM) air quality data that nowadays is based on surface measurements. Three statistical methods for retrieving daily PM2.5 concentrations from satellite products (MODIS-AOD, OMI-AAI) over the San Joaquin Valley (CA) are compared – Linear Regression (LR), Generalized Additive Models (GAM), and Multivariate Adaptive Regression Splines (MARS). Simple LRs show poor correlations in the western USA (R2 ≅ 0.2). Both GAM and MARS were found to perform better than the simple LRs, with a slight advantage to the MARS over the GAM (R2 = 0.71 and R2 = 0.61, respectively). Since MARS is also characterized by a better computational efficiency than GAM, it can be used for improving PM2.5 retrievals from satellite aerosol products. Reliable PM2.5 retrievals can fill in missing surface measurements in areas with sparse ground monitoring coverage and be used for evaluating air quality models and as exposure metrics in epidemiological studies.

Particulate matter (PM), a complex mix of chemical compounds, results to be associated with various health effects. However there is still lack of information on the impact of its different components. PM2.5 and PM1 samples, collected during the different seasons at an urban, rural and remote site, were chemically characterized and the biological effects induced on A549 cells were assessed. A Partial Least Square Discriminant Analysis has been performed to relate PM chemical composition to the toxic effects observed. Results show that PM-induced biological effects changed with the seasons and sites, and such variations may be explained by chemical constituents of PM, derived both from primary and secondary sources. The first-time here reported biological responses induced by PM from a remote site at high altitude were associated with the high concentrations of metals and secondary species typical of the free tropospheric aerosol, influenced by long range transports and aging.

The Moderate Resolution Imaging Spectroradiometer (MODIS) provides daily global coverage, but the 10 km resolution of its aerosol optical depth (AOD) product is not adequate for studying spatial variability of aerosols in urban areas. Recently, a new Multi-Angle Implementation of Atmospheric Correction (MAIAC) algorithm was developed for MODIS which provides AOD at 1 km resolution. Using MAIAC data, the relationship between MAIAC AOD and PM2.5 as measured by the EPA ground monitoring stations was investigated at varying spatial scales. Our analysis suggested that the correlation between PM2.5 and AOD decreased significantly as AOD resolution was degraded. This is so despite the intrinsic mismatch between PM2.5 ground level measurements and AOD vertically integrated measurements. Furthermore, the fine resolution results indicated spatial variability in particle concentration at a sub-10 km scale. Finally, this spatial variability of AOD within the urban domain was shown to depend on PM2.5 levels and wind speed.

Determination of 14C and levoglucosan can provide insights into the quantification of source contributions to carbonaceous aerosols, yet there is still uncertainty on the partitioning of organic carbon (OC) into biomass burning OC (OCbb) and biogenic emission OC (OCbio). Carbonaceous species, levoglucosan and 14C in PM2.5 were measured at three types of site in southeast China combined with Latin hypercube sampling, with the objectives to study source contributions to total carbon (TC) and their uncertainties, and to evaluate the influence of levoglucosan/OCbb ratios on OCbb and OCbio partitioning. It was found reliably that fossil fuel combustion is the main contributor (62.90–72.23%) to TC at urban and peri-urban sites. Biogenic emissions have important contribution (winter, 52.98%; summer, 45.71%) to TC at background site. With the increase in levoglucosan/OCbb ratios, the contribution of OCbio is increased while OCbb is decreased in a pattern of approximate natural logarithm at a given range.

Embryo toxicity of particles generated by combustion processes is of special concern for human health. A significant part of these toxic effects is linked to the binding of some pollutants (like polycyclic aromatic hydrocarbons or PAHs) to the Aryl hydrocarbon Receptor (AhR) and the activation of target genes, like the cytochrome P4501A. This activity was analyzed for ambient air and coal-combustion particle extracts in zebrafish embryos (the cyp1aDarT assay) and in two single-cell bioassays: the yeast-based YCM-RYA and the DR-luc (rat cells) assay. Observed AhR ligand activity of samples generally correlated to the predicted toxic effect according to their PAH composition, except for one of the coal combustion samples with an anomalously high activity in the cyp1aDarT assay. This sample induced deformities in zebrafish embryos. We concluded that the combination of morphological and molecular assays may detect embryonic toxic effects that cannot be predicted from chemical analyses or single-cell bioassays.

We analyzed the source–receptor relationships for particulate polycyclic aromatic hydrocarbon (PAH) concentrations in northeastern Asia using an aerosol chemical transport model. The model successfully simulated the observed concentrations. In Beijing (China) benzo[a]pyren (BaP) concentrations are due to emissions from its own domain. In Noto, Oki and Tsushima (Japan), transboundary transport from northern China (>40°N, 40–60%) and central China (30–40°N, 10–40%) largely influences BaP concentrations from winter to spring, whereas the relative contribution from central China is dominant (90%) in Hedo. In the summer, the contribution from Japanese domestic sources increases (40–80%) at the 4 sites. Contributions from Japan and Russia are additional source of BaP over the northwestern Pacific Ocean in summer. The contribution rates for the concentrations from each domain are different among PAH species depending on their particulate phase oxidation rates. Reaction with O3 on particulate surfaces may be an important component of the PAH oxidation processes.

Lead (Pb) concentrations and isotopic compositions from soils, dusts and aerosols from public land and residential lots adjacent to the copper and Pb mine and smelter at Mount Isa, Australia, were examined to understand the sources and risks of environmental Pb exposure. Urban soil samples contain elevated Pb concentrations (mean 1560 mg/kg), of which 45–85% of the Pb is bioaccessible. The Pb isotopic composition of surface soils (0–2 cm), aerosols and dusts (206Pb/207Pb, 208Pb/207Pb range: 1.049, 2.322–1.069, 2.345) are dominated by Pb derived from the Mount Isa Pb–zinc ore bodies. Underlying soil horizons (10–20 cm) have distinctly different Pb isotopic compositions (206Pb/207Pb, 208Pb/207Pb range: 1.093, 2.354–1.212, 2.495). Surface soil-, dust- and aerosol-Pb are derived predominantly from smelter emissions and fugitive mining sources and not from in situ weathered bedrock. Remediation strategies should target legacy and ongoing sources of environmental Pb to mitigate the problem of Pb exposure at Mount Isa.

Benzo(a)pyrene (BaP) is one of the most dangerous PAH due to its high carcinogenic and mutagenic character. Because of this reason, the Directive 2004/107/CE of the European Union establishes a target value of 1 ng/m3 of BaP in the atmosphere.In this paper, the main aim is to estimate the BaP concentrations in the atmosphere by using last generation of air quality dispersion models with the inclusion of the transport, scavenging and deposition processes for the BaP. The degradation of the particulated BaP by the ozone has been considered. The aerosol–gas partitioning phenomenon in the atmosphere is modelled taking into a count that the concentrations in the gas and the aerosol phases. If the pre-existing organic aerosol concentrations are zero gas/particle equilibrium is established.The model has been validated at local scale with data from a sampling campaign carried out in the area of Zaragoza (Spain) during 12 weeks.