The atmospheric heavy metal pollution of the Fraser Valley, B.C., Canada was assessed in 1993 by analyzing 62 samples of the common woodland moss Isothecium stoloniferum for lead, cadmium, nickel, zinc, chromium, and manganese. The latter two metals did not show a distinct regional distribution, but lead, cadmium, nickel, and zinc showed distinct pattern along a west-east gradient. High values were found in the metropolitan Vancouver area, located in the west of the study region. Significantly lower values were recorded for mosses from the eastern more rural areas of the Fraser Valley. Metal pollutants are likely to be contained close to their emission sources by alternating south-east, north-west winds. Highest values overall were found in the North Shore Mountains, adjacent to Vancouver. This was related to higher precipitation and short range pollutant transport from the industrialized, heavily populated areas in the floodplain of the Fraser River.

The relationship between acidity and benthic invertebrate communities was investigated in two small streams in coniferous forests in central Jutland, Denmark, during 1992 and 1993. Stream pH was acid (mean pH 4.8 and 5.4) and alkalinity fluctuated greatly with mean values around zero. During rain events, water from springfed reaches upstream were mixed downstream with brown humic acid water with high aluminium content, and pH declined from circumneutral near the springs down to pH below 4 over a very short distance (0.5–1.5 km). The benthic invertebrate communities in the most acidic downstream reaches of both streams were dominated by filipalpian stoneflies, mainly Leuctra nigra (Olv.). Community composition remained very similar throughout the sampling period despite variations in pH. In the upper (neutral) reaches invertebrates intolerant of low pH such as Gammarus pulex L. were found. The concentrations of chloride and sulphate in the streams were more than double the concentrations in a nearby moorland stream indicating a strong impact of acidifying atmospheric deposition on the two forest streams. Results of this study indicate that afforestation with conifers on sandy Danish soils with low buffering capacity (about 25% of the total Danish land area) may lead to an increased acidification of surface waters and thereby also to an impoverished aquatic fauna.

To study whether airborne pollution can be detected in overbank sediments, samples collected from five overbank sediment profiles in eastern Finnmark, Norway, at 1 cm depth intervals, were subjected to chemical analysis and ²¹⁰Pb dating. The studied drainage basins constitute parts of an area polluted by emissions from two Ni-Cu smelters in Russia. In the most polluted catchment area, the surface sample showed a 5-fold higher Ni concentration and a 3-fold higher Cu concentration than the pre-industrial sediments at depth. The increases started at the same time as the smelters. Slight Ni increases were also detected in the neighbouring drainage basin, while no significant concentration change was seen in drainage basins previously shown to be only weakly influenced by the smelter emissions. In the most polluted drainage basin, the increase in Ni accumulation rate did not equal the airborne deposition rate. Selective surface erosion of fine grained particles with adhering airborne Ni has probably caused excess Ni accumulation in both overbank and lake sediments. On the contrary, opening of minerogenic point sources may dilute the pollutant concentrations in the drainage sediments. Thus, dating of the sediment profiles is necessary to determine the airborne pollutant accumulation rates. However, dating is not necessary to map the resultant concentration increase, that may show the increased exposure of humans and biota in contact with the sediments.

Estimates of mercury emissions from individual sources and source categories are needed to understand relationships between the emissions and resulting deposition and to evaluate possible approaches to reducing those emissions. We have developed geographically-resolved estimates of annual average mercury emission rates from current anthropogenic sources in the 48 contiguous United States. These estimates were made by applying emission factors to individual facility operating data and to county-wide source activity levels. We apportioned the emissions to an Eulerian modeling grid system using point source coordinates and the fractions of county areas in each grid cell. Point sources account for about 89% of the 48-state total mercury emissions of 146.4 Mg/yr. Most of the emissions in the inventory are from combustion of mercury-containing fossil fuels and municipal waste, located primarily in the mid-Atlantic and Great Lakes states as well as in the Southeast. The major uncertainties in the emission estimates are caused by uncertainties in the emission factors used to develop the estimates. This uncertainty is likely a result of variability in the mercury content of the combusted materials and in the removal of mercury by air pollution control devices. The greatest research need to reduce uncertainties in mercury emission estimates is additional measurements to improve emission factors.