Hexabromocyclododecanes (HBCDs) have been considered candidate persistent organic pollutants, however, environmental data on their presence in China, a major world market, are limited. In this study, airborne particle-bound HBCDs in Shanghai, China were quantified with liquid chromatography–tandem mass spectrometry, and their total concentrations varied from 3.21 to 123 pg/m³. The industrial area showed about three times higher HBCD levels than the urban areas. Gamma-HBCD dominated in particle-associated HBCDs in the industrial area, while α-HBCD was the major diastereomer of the urban areas, which is quite different from the pattern of technical products. Besides α-, β- and γ-HBCDs, δ-HBCD was also detected in all samples (0.09–6.31 pg/m³), while no ɛ-HBCD was found. Airborne β- and γ-HBCDs were racemic in most studied areas due to their chiral signatures showing no significant difference from commercial mixture. Fractions of (+)-α-HBCD (0.417–0.467), however, suggested the enrichment of (−)-α-HBCD and the involvement of enantioselective bioprocesses.

High levels of polybrominated diphenyl ethers (PBDEs) have been extensively reported in urban areas and at e-waste recycling sites in coastal China. However, data are scarce in northern China and are not available in rural areas at all. In addition, it is often believed that air concentrations in rural areas are lower than those in urban areas without distinguishing rural residential areas and open fields. In this study, air samples were collected at 17 sites covering urban and rural (residential and open field) areas in northern China using active samplers. With BDE-209 dominated in all congeners, the average concentrations of BDE-209 (41 ± 72 pg/m³) and other 13 PBDEs (16 ± 12 pg/m³) were significantly lower than those found in south China, such as in Guangzhou or Hong Kong. On average, the total PBDE concentrations at the urban sites were 2.2 and 2.9 times of those at the rural residential and field sites, respectively.

For a given emissions inventory, the general levels of air pollutants and the spatial distribution of their concentrations are determined by the physiochemical state of the atmosphere. Apart from the trivial seasonal and daily cycles, most of the variability is associated with the atmospheric synoptic scale. A simple methodology for assessing future levels of air pollutants' concentrations based on synoptic forecasts is presented. At short time scales the methodology is comparable and slightly better than persistence and seasonal forecasts at categorical classification of pollution levels. It's utility is shown for air quality studies at the long time scale of a changing climate scenario, where seasonality and persistence cannot be used. It is demonstrated that the air quality variability due to changes in the pollution emissions can be expected to be much larger than that associated with the effects of climatic changes.

We studied the effect of estimated PM₁₀ on respiratory infections in children from Cordoba, Argentine as well as the influence of weather factors, socio-economic conditions and education. We analyzed upper and lower respiratory infections and applied a time-series analysis with a quasi-Poisson distribution link function. To control for seasonally varying factors we fitted cubic smoothing splines of date. We also examined community-specific parameters and differences in susceptibility by sex. We found a significant association between particles and respiratory infections. This relationship was affected by mean temperature, atmospheric pressure and wind speed. These effects were stronger in fall, winter and spring for upper respiratory infections while for lower respiratory infections the association was significant only during spring. Low socio-economic conditions and low education levels increased the risk of respiratory infections. These findings add useful information to understand the influence of airborne particles on children health in developing countries.

Orange trees are widely cultivated in regions with high concentrations of tropospheric ozone. Citrus absorb ozone through their stomata and emit volatile organic compounds (VOC), which, together with soil emissions of NO, contribute to non-stomatal ozone removal. In a Valencia orange orchard in Exeter, California, we used fast sensors and eddy covariance to characterize water and ozone fluxes. We also measured meteorological parameters necessary to model other important sinks of ozone deposition. We present changes in magnitude of these ozone deposition sinks over the year in response to environmental parameters. Within the plant canopy, the orchard constitutes a sink for ozone, with non-stomatal ozone deposition larger than stomatal uptake. In particular, soil deposition and reactions between ozone, VOC and NO represented the major sinks of ozone. This research aims to help the development of metrics for ozone-risk assessment and advance our understanding of citrus in biosphere-atmosphere exchange.

Fifteen polybrominated diphenyl ethers (PBDEs) and eighteen non-PBDEs were measured in 116 dust samples collected from homes in Vancouver, Canada during 2007–2008 as part of the Chemicals Health and Pregnancy (CHirP) study. The highest concentrations of PBDEs in house dust were observed for BDE 209, with a median concentration of 1350 ng/g. This is about two times greater than the median concentration of the PentaBDE (represented by the most abundant compounds in this formulation, ΣBDE 47, 99 and 100). In the case of non-PBDE FRs, a detection frequency between 81% and 100% was observed for nine analytes including: HBCD, BTBPE, BEHTBP, EHTBB, HBB, PBTO, PBBe, ATE and DP. The high detection of new FRs in indoor environments reflects their ubiquitous presence in indoor environment due to regulation of the PBDEs. Exposure to FRs are estimated based on these data for adults and toddlers.

Air quality improvement by a forested, peri-urban national park was quantified by combining the Urban Forest Effects (UFORE) and the Weather Research and Forecasting coupled with Chemistry (WRF-Chem) models. We estimated the ecosystem-level annual pollution removal function of the park’s trees, shrub and grasses using pollution concentration data for carbon monoxide (CO), ozone (O₃), and particulate matter less than 10 microns in diameter (PM₁₀), modeled meteorological and pollution variables, and measured forest structure data. Ecosystem-level O₃ and CO removal and formation were also analyzed for a representative month. Total annual air quality improvement of the park’s vegetation was approximately 0.02% for CO, 1% for O₃, and 2% for PM₁₀, of the annual concentrations for these three pollutants. Results can be used to understand the air quality regulation ecosystem services of peri-urban forests and regional dynamics of air pollution emissions from major urban areas.

Growing attention is devoted to understand the influence of the short-term variations in air concentrations on the environmental fate of semivolatile organic compounds (SVOCs) such as polycyclic aromatic hydrocarbons (PAHs). These variations are ascribable to factors such as temperature-mediated air-surface exchange and variability of planetary boundary layer (PBL) height and structure. But when investigating the fate of SVOCs at a local scale, further variability can derive from specific point source contributions. In this context, a new modeling approach (AirPlus) which integrates a previously developed model (AirFug) with an air dispersion model (AERMOD) is presented. The integrated model is illustrated for two PAHs in a Northern Italy scenario. Results show how chemical contributions deriving from background advective inflows, local emissions and a point source interact in an hourly-varying meteorological scenario to determine air concentration rapid changes and the consequent response of the soil compartment.

Mercury (Hg) in autumn litterfall from predominately deciduous forests was measured in 3 years of samples from 23 Mercury Deposition Network sites in 15 states across the eastern USA. Annual litterfall Hg dry deposition was significantly higher (median 12.3 micrograms per square meter (μg/m²), range 3.5–23.4 μg/m²) than annual Hg wet deposition (median 9.6 μg/m², range 4.4–19.7 μg/m²). The mean ratio of dry to wet Hg deposition was 1.3–1. The sum of dry and wet Hg deposition averaged 21 μg/m² per year and 55% was litterfall dry deposition. Methylmercury was a median 0.8% of Hg in litterfall and ranged from 0.6 to 1.5%. Annual litterfall Hg and wet Hg deposition rates differed significantly and were weakly correlated. Litterfall Hg dry deposition differed among forest-cover types. This study demonstrated how annual litterfall Hg dry deposition rates approximate the lower bound of annual Hg dry fluxes.

Long-term fluxes of CO₂, and combined short-term fluxes of CH₄ and CO₂ were measured with the eddy covariance technique in the city centre of Florence. CO₂ long-term weekly fluxes exhibit a high seasonality, ranging from 39 to 172% of the mean annual value in summer and winter respectively, while CH₄ fluxes are relevant and don’t exhibit temporal variability. Contribution of road traffic and domestic heating has been estimated through multi-regression models combined with inventorial traffic and CH₄ consumption data, revealing that heating accounts for more than 80% of observed CO₂ fluxes. Those two components are instead responsible for only 14% of observed CH₄ fluxes, while the major residual part is likely dominated by gas network leakages. CH₄ fluxes expressed as CO₂ equivalent represent about 8% of CO₂ emissions, ranging from 16% in summer to 4% in winter, and cannot therefore be neglected when assessing greenhouse impact of cities.