Methylmercury (MeHg), dissolved organic carbon (DOC), and sulfate (SO₄ ⁼) relationships were investigated in the mining-influenced St. Louis River watershed in northeast Minnesota. Fewer wetlands and higher SO₄ ⁼ in the mining region lead to generally lower availability and solubility of DOC in mining streams compared to non-mining streams. MeHg concentrations, however, are similarly low in mining and non-mining streams during low flow periods, implying that the extra DOC found in non-mining streams carries little MeHg with it during these periods. High water levels elevated MeHg concentrations in both stream types owing to release from wetlands of DOC species that contain MeHg and remain relatively soluble in streams with elevated ionic strength. In-river methylation appeared to be a negligible component of the MeHg budget for the St. Louis River during this study as MeHg and DOC concentrations were intermediate to those observed in its mining-influenced and wetland-dominated tributaries.

Transfer of aqueous methylmercury (MeHg) to primary consumers in aquatic foodwebs is poorly understood despite its importance for bioaccumulation of MeHg. We studied bioaccumulation of MeHg in simple aquatic food chains of two humic boreal streams in relation to streamwater chemistry, food web characteristics and dietary fatty acid (FA) biomarkers. Transfer of aqueous MeHg into primary consumers was similar in both streams, resulting in higher MeHg in consumers in the MeHg-rich stream. Trophic enrichment of MeHg and dietary retention of FA biomarkers was the same in both streams, suggesting that exposure to aqueous MeHg at the base of the food chain determined levels of MeHg in biota. In addition, contents of dietary biomarkers suggested that ingestion of algae reduced MeHg bioaccumulation, while ingestion of bacteria stimulated MeHg uptake. Dietary uptake of bacteria could thus be an important pathway for MeHg-transfer at the bottom of food chains in humic streams.

∑₃₀PAH gas phase concentrations (13–86 and 22–40 ng m⁻³ in the Mediterranean and Black Seas, respectively) dominated the atmospheric levels due to the high contribution of phenanthrene, dibenzothiophene and their alkylated derivates. The high variability of PAH atmospheric concentrations in the different sub-basins is due to several factors (i.e. air-mass trajectory, proximity to sources and losses by deposition). The ∑₃₀PAH atmospheric deposition (dominated by low MW PAH net air–water diffusive fluxes) is estimated to be ∼3100 ton y⁻¹ (Mediterranean) and ∼500 ton y⁻¹ (Black Sea). Net volatilization for certain PAHs was estimated. Deposition fluxes (1–2 orders of magnitude higher than reported PAH settling fluxes in the water column) confirm an important depletion/sink of water column PAH in the photic zone, especially for low MW PAHs. Degradation processes in the water column may be responsible for this decoupling. Conversely, high MW PAHs dry deposition fluxes are similar to their settling fluxes.

Arsenic (As) reduction and translocation are key processes for As hyperaccumulation by the hyperaccumulator Pteris vittata L. Micro-X-ray adsorption spectroscopy of P. vittata’s rhizoid tissues revealed that As reduction mainly occurred in endodermis during translocation from epidermis to vascular bundle. Prior to reduction, arsenate (As (V)) translocation was an active process requiring energy and employing a phosphate (P) transporter. Use of a synchrotron X-ray microprobe showed that As (V) and P were cotransported and that this process could be enhanced by As (V) exposure or P deficiency but restrained by energy release inhibition caused by 2,4-dinitrophenol or sodium orthovanadate. In contrast, after As reduction, As(III) translocation differed from P translocation and was more efficient, appearing free from the apparent endodermal blockage. The results here revealed the role of the P transporter on As translocation as well as the key role of As reduction in As hyperaccumulation by P. vittata.

For more than 50 years perfluoroalkyl substances (PFASs) have found worldwide industrial and household uses. Some PFASs are presumed to be persistent and bioaccumulative. Roe deer (Capreolus capreolus) are thought to be a suitable bioindicator for the accumulation of organic xenobiotics. Due to the ubiquitous nature of PFASs in the environment a retrospective study on temporal trends was carried out. A total of 110 deer liver pools collected from 1989 to 2010 in Germany were analyzed for their levels of PFASs. The highest concentrations were measured for perfluorooctane sulfonate (PFOS) (median 6.3 μg/kg). Perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA) and perfluorodecanoic acid (PFDA) were detected with median concentrations of 0.5 μg/kg, 1.2 μg/kg and 0.3 μg/kg, respectively, while concentrations of the other PFASs were below the limit of quantification. PFOS concentrations decreased significantly (rₛ = −0.741; p = <0.0001) from 9.2 μg/kg in 2000 to 1.8 μg/kg in 2010.

This work presents the influence of sugarcane burning on PAH levels and their profiles at a residence located in Araraquara (SP, Brazil), a city surrounded by sugarcane plantations. The average concentrations of total PAHs (ΣPAHs) associated with atmospheric particulate matter were higher during the burning period (ΣPAHs 22.9 ng m⁻³) than in the non-burning period (ΣPAH 2.35 ng m⁻³). A comparison of our results with previous studies regarding PAH levels and their profiles in Araraquara outdoor air indicated that sugarcane burning was the main PAH air source in the indoor harvesting season samples. The benzo[a]pyrene equivalent (BaPₑq) was used for cancer risk assessment, and higher average values were obtained in the harvesting season air samples (1.7 ng m⁻³) than in the non-harvesting air samples (0.07 ng m⁻³). These findings suggest that sugarcane burning during the harvesting season can represent a public health risk in affected cities.

Food production by urban dwellers is of growing importance in developing and developed countries. Urban horticulture is associated with health risks as crops in urban settings are generally exposed to higher levels of pollutants than those in rural areas. We determined the concentration of trace metals in the biomass of different horticultural crops grown in the inner city of Berlin, Germany, and analysed how the local setting shaped the concentration patterns. We revealed significant differences in trace metal concentrations depending on local traffic, crop species, planting style and building structures, but not on vegetable type. Higher overall traffic burden increased trace metal content in the biomass. The presence of buildings and large masses of vegetation as barriers between crops and roads reduced trace metal content in the biomass. Based on this we discuss consequences for urban horticulture, risk assessment, and planting and monitoring guidelines for cultivation and consumption of crops.

This work presents a diagnostic methodology in support to source apportionment studies to identify remote and local pollution sources. It is based on the temporal analysis of both PM size distributions and PM size fraction correlation along with natural radioactivity measurements as index of Planetary Boundary Layer dynamic. A correlation drop is indicative of changing aerosol sources. When this observation is coupled with decreasing level of natural radioactivity and increasing aerosol concentration, be it coarse or fine, it is indicative of the inflow of remote polluted air masses. The methodology defines in which size range operates the contribution of remote pollution sources. It was applied to two PM10 pollution episodes: the first involved the advection of coarse PM, the second entailed the inflow of two air masses, one transporting coarse dust and the other fine PM. Dust models and backward trajectories analysis confirmed such results, indicating the air mass provenience.

Since early 1980s, chemical pollution has become a serious environmental problem in rapidly developing China. This study reviewed the policy and legal framework for monitoring and management of chemical pollutants in China, with reference to the relevant experience in other jurisdictions. Although efforts in environmental monitoring of chemical contamination have been substantially increased over the last decade, China is lagging behind in terms of nationwide monitoring of chemical contamination in human population, and standardization of sampling and analytical protocols. While actively participating in various international treaties and conventions related to pollution control, China also has a very comprehensive set of environmental laws and policies. These include the newly enacted legislation on the control of new chemicals (i.e., China REACH) and the development of a set of National Environmental Standards. In addition to environmental education, these new measures will further enhance the control of chemical pollutants and facilitate effective law enforcement.