A plot-scale, rainfall-simulation study measured edge-of-field pollutant losses from conventional-till, strip-till, and no-till treatments in a burley tobacco production system. The field experiment results show that the conventional-till treatment yielded more total runoff than strip- and no-till treatments. Compared to the conventional-till treatment, both no-till and strip-till reduced the total mass losses of total suspended solids (TSS), total nitrogen (TN), total Kjeldahl nitrogen (TKN), nitrate (NO-N), ammonia (NH₃-N), total phosphorus (TP), orthophosphate (PO₄-P), and the insecticide chlorpyrifos in runoff. Although statistical analyses indicated that there was no significant difference between the no-till and strip-till practices, the no-till practice consistently yielded less edge-of-field pollutant loss than the strip-till practice. This research reinforces the body of knowledge documenting the effectiveness of conservation-tillage practices in reducing edge-of-field pollutant losses.

The aim of this study was examination possibility of Azolla caroliniana Willd. to aerate its medium enriched with Cd(II) and Hg(II) and comparison of DO and ODR methods in measurement aeration status of solutions. Azolla system has been chosen to verify the validity of the measuring ODR method in water solution. Water aeration measurements, one of important environmental tests, are performed most often by measurement of dissolved oxygen with oxygen sensors. Other similar method called oxygen diffusion rate is generally used in different porous materials such as soil. Our first objective was to check if these both methods are comparable and may be use exchangeable in water solution. The both types of measurements were performed in medium saturated at different oxygen concentrations. The linear relationship and high correlation (R = 0.89) were found between values of ODR and DO. The object of the second part of our studies was A. caroliniana Willd. (Azollaceae), a floating water fern living in symbiosis with cyanobacterium Anabaena azollae Strasb. (Nostoceae) that fixes atmospheric nitrogen. Azolla plants are used for centuries as a nitrogen biofertilizer. The second aim of our work was to find out, if the fern reduces or increases oxygen concentration in water. The ODR method was used to determine the aeration status of the nutrient solution. During 12 days of the experiment at laboratory conditions, an active role of A. caroliniana in aeration of the nutrient solution containing Cd(II) and Hg(II) was stated.

Critical loads have been successfully used within Europe in the development of effects-based policies for pollution abatement, including the Second Sulphur Protocol and the Protocol to abate acidification, eutrophication and ground-level ozone (CLRTAP, 1979). This success has encouraged the UK Environment Agency and Conservation Agencies to use the national critical load maps as a screening tool in assessing the threats from acidification and eutrophication to designated (Natura 2000) sites. The UK maps of critical loads are based on national-scale data sets appropriate for national-scale assessments, and were never intended for use at the site-specific level. Site-based assessments are often targeted at Special Areas of Conservation, a sub-set of the UK Natura 2000 sites. The spatial data available includes the boundaries of the sites but not the location of the designated features. Ancillary data is variable from one site to another; habitat types may be described in detail with cross-reference to classes of the National Vegetation Classification (NVC: Rodwell, 1991 et seq), but information available on soils and geology is generalised and has not been related to the habitats or species being protected. Hence it can be difficult to relate the individual sites to the national maps, even where appropriate to do so. This paper examines the underlying uncertainties in the national critical load maps showing how the maps could give misleading results if used for site-specific assessments. It also includes advice on how to determine when the national data may be appropriate as a policy-tool at the site-level.

Plant uptake is a major pathway by which toxic metals can enter the food chain. In this laboratory study we grew spinach, radish, and perennial ryegrass on sand blends containing 50% waste foundry sand (WFS) to assess the availability of Al, B, Ba, Be, Cd, Co, Cr, Cu, Fe, Mg, Mn, Mo, Ni, Pb, V, and Zn. The WFSs utilized in this study were from aluminum, iron, and steel foundries. Although there were differences in the amounts of metals accumulated by the various plant species, excessive amounts of heavy metals were not taken up, regardless of WFS treatment. In spinach and radish, B, Cu, Fe, Mn and Zn were found to be within or close to the sufficiency range for agronomic crops. In ryegrass cuttings at 27, 57, and 87 days, Cu and Zn were within sufficiency ranges, but plants were Fe deficient and contained elevated concentrations of B, Mn, and Mo. Data from this study will be useful for state regulatory agencies interested in developing beneficial use regulations for WFSs.

For the routine determination of metals in environmental samples, we require microwave-assisted digestion methods that yield 'total' or 'near-total' recoveries while avoiding the use of HF acid. As inductively coupled plasma mass spectrometry (ICP-MS) is the method of detection, it is desirable to minimize the use of HCl to avoid spectral interferences caused by high Cl- concentrations. Using certified reference materials, we performed a series of modifications to the US EPA method 3051 which included: increasing the temperature and durations of microwave digestion, varying the ratio of sample mass to acid volume, and alterations to the compositions of the acid digestion mixture. The experiments were conducted using urban particulate matter (NIST-1648), coal fly ash (NBS-1633) and six CANMET certified reference materials (Till-2, Till-3, Till-4, LKSD-1, LKSD-2 and LKSD-4), in two laboratories (Health Canada and Environment Canada) using different microwave digestion systems and different ICP-MS instruments. Our modified microwave-assisted nitric acid digestion method improved recoveries for Pb, Zn, V, Fe and Cu approaching 'total' recoveries in the same matrices determined using X-ray fluorescence (XRF) and instrumental neutron activation analysis (INAA) as reported in the certificates of analysis. Recoveries for other elements such as Cr and Ni compared well with 'near-total' recoveries yielded by traditional (non-assisted) acid digestion methods.

In response to reduced sulphur emissions, there has been a large decrease in sulphate ( [graphic removed] ; -0.97 μeq l-¹ year-¹) and hydrogen (-1.18 μeq l-¹ year-¹) ion concentration in bulk precipitation between 1980 and 2000 at Plastic Lake in central Ontario. The benefit of this large reduction in [graphic removed] deposition on stream water chemistry was assessed using the gauged outflow from a conifer-forested catchment (PC1; 23.3 ha), which is influenced by a small wetland located immediately upstream of the outflow. Sulphate concentrations declined, but not significantly due to large inter-annual variation in [graphic removed] concentration. Between 1980 and 2000, there were significant increases in dissolved organic carbon, ammonium and potassium concentration likely reflecting increased mineralisation in the wetland. Calcium concentrations in PC1 decreased during the two decade period (-2.24 μeq l-¹ year-¹), as a consequence there was no improvement in stream pH and the Ca:Al ratio in PC1 continued to decline. A similar response was noted in an upland-draining sub-catchment of PC1-08 that has been monitored since 1987. Despite large reductions in [graphic removed] deposition and almost complete retention of nitrogen in soil, there has been no improvement (in terms of pH) in stream water at PC1 due to a combination of soil acidification and climatic (droughts, increased mineralisation) perturbations.

We used laboratory experiments to investigate surface resistance (R c) to dry deposition of ozone (O₃) on different types of soil samples collected from the arid deserts and the Loess Plateau of northern China. Furthermore, we measured the factors that affected R c, which depends on the physical and chemical interaction between trace constituents and the deposition surface, and evaluated deposition velocity (V d). There was little influence of geometric surface area, soil weight, or O₃ concentration on V d of O₃. The effect of relative humidity (RH) (i.e. moisture content of the soil) on O₃ uptake was in agreement with results reported in the literature: a distinct RH dependence of V d and little uptake under water-saturated conditions were observed. R c values for all the soil samples examined were in the range 0.21-3.3 s mm-¹ and were exponentially related to the surface area of the particles and the organic carbon content of each soil sample at RH of both <10 and 60%.

This study deals with Particle Matter (PM) levels in the metropolitan area of Lisbon and shows that EU directive is exceeded in a systematic way, mainly due to the inner city traffic. Results show that it is important to develop an epidemiological study in Lisbon to find a possible association between PM levels, sources and morbidity. Some important issues related with a monitor's representation of regional, sub-regional, and local air pollution exposures to the population in the metropolitan area are highlighted. PM₂.₅ and PM₁₀ total mass concentration measured in several places located in both centre of Lisbon and the outskirts are quite well correlated, mainly considering that two measuring methodologies (automatic and gravimetric) were used and areas with different classifications (urban and suburban) were analysed. However, the results imply that a source-oriented evaluation of PM health effects needs to take into account the uncertainty associated with spatial representativity of the species measured at a single sampling station. Temporal correlation across sampling stations, within relatively short separation distances, varied considerably for some important elements (Zn, Sb, Cu, As and Br), indicating that the precision of population exposure estimates for specific elements can vary depending on the species.

Inter-annual variability of surface ozone (O₃) and nitrogen dioxide (NO₂) over Europe has been studied over the period 1958-2003 using a three-dimensional Chemistry-Transport Model coupled to meteorological data from the ERA40 data set produced at the European Centre of Medium-range Weather Forecasts (ECMWF). Emissions and boundary conditions were kept at present levels throughout the simulation period. It was found that the annual mean NO₂ concentration varies between ±50% and the summer mean O₃ concentration varies between -10 and +20 percent (%) compared to the 46-year average over the model domain. There is also variation in ozone and NO₂ over longer time scales. The last 22 years display high concentrations of ozone in central and south-western Europe and low concentrations in north-eastern Europe. The first 22 years display very high concentrations of NO₂ over the North Sea. There is indication of trends in ozone and nitrogen dioxide but this has to be investigated further. Such information is one factor that should be taken into account when considering future control strategies.

Analytical procedure for the determination of exchangeable Cr(VI) was developed. In order to optimise the extraction procedure, the efficiency of extraction of exchangeable Cr(VI) in soil samples was investigated in KH₂PO₄-K₂HPO₄ buffer solutions (0.015 up to 0.2 mol l-¹), adjusted to the pH of the soil. Phosphate buffer was used to efficiently desorb Cr(VI) from soil particles. The extraction time (mechanical shaking) ranged from 1 up to 72 h. Cr(VI) in soil extracts was determined by anion-exchange fast protein liquid chromatography with electrothermal atomic absorption detection (FPLC-ETAAS). The study was performed on soil samples from the field treated with the tannery waste for seventeen years. Samples were analysed in the 16 year after the last waste application. It was experimentally proven that the optimal phosphate buffer concentration was 0.1 mol l-¹ and extraction time 16 h. An additional experiment was done to confirm that during the extraction, soluble Cr(III) was not oxidised to Cr(VI) by Mn(IV) oxides present in soil samples. For this purpose soil with the same characteristics, but not treated with tannery waste, was spiked with Cr(III) and the analytical procedure performed. No measurable Cr(VI) concentrations were detected. The repeatability of measurement was 2.5%, while the reproducibility of measurement was 6.9%. The accuracy of the analytical procedure was tested by spiking of soil samples with Cr(VI). The recoveries were better than 95%. The analytical procedure with limit of detection (LOD) 15 ng g-¹ of Cr(VI) was sensitive enough for the determination of exchangeable Cr(VI) in soils. In field soil samples analysed the concentrations of exchangeable Cr(VI) were found to be about 200 ng g-¹.