Rhizosphere soil and dominant plant samples were collected at a brownfield site in New Jersey, USA, during summer 2005 to evaluate plant metal uptake from the contaminated soils. Metal concentrations varied from 4.25 to 978 μg g⁻¹ for As, 9.68–209 μg g⁻¹ for Cr, 23.9–1870 μg g⁻¹ for Cu, and 24.8–6502 μg g⁻¹ for Zn. A wide range of metal uptake efficiencies in the roots, stems and leaves was found in this study. Data showed that (1) Betula populifolia has high Zn, Cu and As accumulations in the root, and high concentrations of Cu and Zn in the stem and the leaf; (2) Rhus copallinum has high accumulation of Zn and Cr in the leaf and Cu in the stem; (3) Polygonum cuspidatum has high accumulations of Cu and As in the root; and (4) Artemisia vulgaris shows high Cu accumulation in the leaf and the stem.

Polychlorinated naphthalenes (PCNs) are now under review by the Stockholm Convention as a candidate for POPs for their persistence, toxicity, bioaccumulation, and long-range atmospheric transport. Data regarding PCN levels and their environmental fate are sparse in China. The PCN concentration and distribution in soils of the Pearl River Delta were reported, and the average total concentration was 59.9 ± 86.7 pg/g. Tri-CNs was the dominant homologue group, and CN 24 was the most abundant congener. A gradient of PCN levels between more and less developed areas was observed. Based on fugacity fraction results, CN 51 is proposed as a possible source marker for specific combustion emissions. Air-soil exchange of PCNs was estimated by calculating the soil and air fugacity. Fugacity fraction values indicated that tri- to penta-CNs were closer to equilibrium in winter and toward net volatilization in summer, while hexa-CNs experienced net air-to-soil transfer in both seasons.

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.

Seasonal variation in mercury (Hg) concentrations and food web structure was assessed for eastern Lake Ontario. Hg concentrations, measured in 6 species of invertebrates and 8 species of fishes, tended to be highest in the spring and lowest in the summer for most biota. Yellow perch (Perca flavescens) exhibited significant ontogenetic shifts in diet and Hg, although such patterns were not evident for other species. Food web structure, as indicated by stable isotope values (δ¹⁵N, δ¹³C) was not static. Log-transformed Hg data were strongly and consistently correlated with δ¹⁵N values for the whole food web in each of the three seasons (slopes, 0.17–0.24) and across the entire year (slope, 0.2). While significantly different between seasons, the regression slope values are still consistent with published global Hg biomagnification rates. Our results indicate that the assessment of Hg trends in Great Lakes must take into account seasonal patterns and time of sampling.

The concentration and composition of PAHs emitted from biomass cooking fuel were characterized in a rural non-smoking household in northern China. Twenty-two parent PAHs (pPAHs), 12 nitro-PAHs (nPAHs), and 4 oxy-PAHs (oPAHs) were measured in the kitchen, bedroom, and outdoors during both summer and winter. The most severe contamination occurred in the kitchen in the winter, where the daily mean concentrations of pPAHs, nPAHs, and oPAHs were 7500 ± 4100, 38 ± 29, and 8400 ± 9200 ng/m³, respectively. Our results suggest that the nPAHs were largely from secondary formation in ambient air while oPAHs were either from primary emission of biomass burning or secondary formation from pPAHs in the kitchen. The daily mean benzo(a)pyrene equivalent exposure concentration was as high as 200 ± 160 ng/m³ in the winter for the housewife who did the cooking compared to 59 ± 37 ng/m³ for the control group that did not cook.

The study examined weekday–weekend differences in ozone, NOₓ (NO and NO₂) and VOC concentrations in Santiago, Chile, from 1999 to 2007. The results provide evidence for the occurrence of an atmospheric phenomenon that produces higher ozone concentrations during weekends despite lower concentrations of ozone precursors. This phenomenon is known as the weekend effect (WE). The overall ozone decrease since the spring of 2004 was a consequence of the implementation of several urban pollution control measures. Although these measures caused a decline in the number of days that exceed the national standard from two-thirds to one-third of summer days, the WE, which became statistically significant beginning in September 2004, could not be eliminated. Furthermore, VOC/NOₓ ratios decreased during the same period (2004), especially in the most industrialized area of Santiago. Similarly, under these regimes, the VOC/NOₓ ratios were higher on Sundays than on weekdays and caused higher ozone concentrations on Sundays.

The interaction of atmospheric sulphur (S) was investigated within the canopies of two boreal forests in Québec, Canada. The net canopy exchange approach, i.e. the difference between S–SO₄ in throughfall and precipitation, suggests high proportion of dry deposition in winter (up to 53%) as compared to summer (1–9%). However, a 3.5‰ decrease in δ¹⁸O–SO₄ throughfall in summer compared to incident precipitation points towards a much larger proportion of dry deposition during the warm season. We suggest that a significant fraction of dry deposition (about 1.2 kg ha⁻¹ yr⁻¹, representing 30–40% of annual wet S deposition) which contributed to the decreased δ¹⁸O–SO₄ in throughfall was taken up by the canopy. Overall, these results showed that, contrary to what is commonly considered, S interchanges in the canopy could be important in boreal forests with low absolute atmospheric S depositions.

Short chain chlorinated paraffins (SCCPs) are semi-volatile chemicals that are considered persistent in the environment, potential toxic and subject to long-range transport. This study investigates the concentrations and gas-particle partitioning of SCCPs at an urban site in Beijing during summer and wintertime. The total atmospheric SCCP levels ranged 1.9–33.0 ng/m³ during wintertime. Significantly higher levels were found during the summer (range 112–332 ng/m³). The average fraction of total SCCPs in the particle phase (ϕ) was 0.67 during wintertime but decreased significantly during the summer (ϕ = 0.06). The ten and eleven carbon chain homologues with five to eight chlorine atoms were the predominant SCCP formula groups in air. Significant linear correlations were found between the gas-particle partition coefficients and the predicted subcooled vapor pressures and octanol–air partition coefficients. The gas-particle partitioning of SCCPs was further investigated and compared with both the Junge–Pankow adsorption and Kₒₐ-based absorption models.

This study was designed to biomonitor the effect of PAH extracts from urban areas on the DNA of lung cell cultures. The analyses of the polycyclic aromatic hydrocarbons (PAHs) were performed in atmospheric PM₂.₅ and PM₁₀ collected at three sampling sites with heavy traffic located in the Metropolitan Area of Porto Alegre (MAPA) (Brazil). The concentrations of 16 major PAHs were determined according to EPA. Comet assay on V79 hamster lung cells was chosen for genotoxicity evaluation. Temperature, humidity, and wind speed were recorded. With regard to the damage index, higher levels were reported in the extract of particulate matter samples from the MAPA during the summer. High molecular weight compounds showed correlation with DNA damage frequency and their respective carcinogenicity.

Litterfall is believed to be the major flux of Hg to soils in forested landscapes, yet much less is known about this input on tropical environment. The Hg litterfall flux was measured during one year in Atlantic Forest fragment, located within Rio de Janeiro urban perimeter, in the Southeastern region of Brazil. The results indicated a mean annual Hg concentration of 238 ± 52 ng g⁻¹ and a total annual Hg deposition of 184 ± 8.2 μg m⁻² y⁻¹. The negative correlation observed between rain precipitation and Hg concentrations is probably related to the higher photosynthetic activity observed during summer. The total Hg concentration in leaves from the most abundant species varied from 60 to 215 ng g⁻¹. Hg concentration showed a positive correlation with stomatal and trichomes densities. These characteristics support the hypothesis that Tropical Forest is an efficient mercury sink and litter plays a key role in Hg dynamics.