Pre-Colombian Mercury Pollution Associated with the Smelting of Argentiferous Ores in the Bolivian Andes

The development of the mercury (Hg) amalgamation process in the mid-sixteenth century triggered the onset of large-scale Hg mining in both the Old and New Worlds. However, ancient Hg emissions associated with amalgamation and earlier mining efforts remain poorly constrained. Using a geochemical time-series generated from lake sediments near Cerro Rico de Potosí, once the world’s largest silver deposit, we demonstrate that pre-Colonial smelting of Andean silver ores generated substantial Hg emissions as early as the twelfth century. Peak sediment Hg concentrations and fluxes are associated with smelting and exceed background values by approximately 20-fold and 22-fold, respectively. The sediment inventory of this early Hg pollution more than doubles that associated with extensive amalgamation following Spanish control of the mine (1574–1900 AD). Global measurements of [Hg] from economic ores sampled world-wide indicate that the phenomenon of Hg enrichment in non-ferrous ores is widespread. The results presented here imply that indigenous smelting constitutes a previously unrecognized source of early Hg pollution, given naturally elevated [Hg] in economic silver deposits.     

The ozone source–receptor model – A tool for UK ozone policy

The Ozone Source–Receptor Model (OSRM) is a Lagrangian trajectory model developed to describe photochemical ozone production in the UK. The OSRM builds on existing boundary layer trajectory models used previously for assisting the development of UK ozone policy, but has a number of notable differences. A novel feature of the OSRM is a surface conversion module to represent the vertical gradient in ozone arising from chemical loss and deposition to the surface. This has significantly improved the performance of the model, especially in urban areas. In this paper, the modelling system is described and its performance against measured ozone concentrations and metrics and other UK ozone models is discussed. The model has been used to calculate future ozone concentrations in the UK and thus to assess a number of possible control measures developed for the UK Air Quality Strategy.     

Verifying emission factors and national POPs emission inventories for the UK using measurements and modelling at two rural locations

Different approaches are used to verify the adequacy of emission factors (EFs) and their use in emission inventories of persistent organic pollutants (POPs). The applicability of EFs was tested using atmospheric dispersion modelling to predict atmospheric concentrations of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) and resulting toxic equivalents (SigmaTEQ) and particulate matter <10 microm (PM(10)) in two rural locations in northern England (UK). The modelling was based on general assumptions of fuel composition, consumption and heating needs to simulate emissions of POPs from the domestic burning of coal and wood where ambient measurements were made in the winter of 1998. The model was used to derive the local contribution to ambient air concentrations, which were estimated independently based on comparative air measurements. The results support the hypothesis that in both villages, the majority of PAHs and the lower chlorinated PCDFs were locally released. The situation for PCBs and polychlorinated naphthalenes (PCNs) was different. While the EFs show the release of both compound groups from the domestic burning of coal and wood, the ambient levels of these "legacy POPs" in the villages were still clearly dominated by other sources. Rural areas relying mainly on fossil fuels can exceed the proposed UK ambient air quality standard for benzo[a]pyrene during winter. The measured EFs were then used to estimate the importance of the domestic burning of coal and wood to national emission inventories for these compound classes. Extrapolations to the UK suggest that the domestic burning of pure wood and coal were minor emitters for chlorinated POPs but contributed strongly to PAH and PM(10) levels in 2000. Finally, the UK's national POPs emission inventories based on source inventories and EF, as used here, were compared to estimates derived using the increase in atmospheric concentration of selected POPs.     

A ranking index to characterize polynuclear aromatic pollutants in environmental samples

This study investigated the use of a screening procedure to provide a ranking index (RI) for characterizing polynuclear aromatic (PNA) species in atmospheric samples. The ranking procedure employs a cost-effective and rapid screening technique based on synchronous luminescence spectroscopy. The efficacy and usefulness of the ranking procedure are demonstrated by comparing the RI values with data expressed in terms of the benzene-soluble standard, benzo[a]pyrene values, and the total content of fourteen PNA compounds.