From 1990 to 1994, a total of 21 sediment cores and 37 grab sediment samples were collected from the Milwaukee Harbor Estuary. Each sediment core was sectioned and dated using ²¹⁰Pb and¹³⁷ Cs radioisotope techniques. A total of 305 samples were analyzed for sixteen polycyclic aromatic compounds (PAHs). Grain size distribution, porosity, and total organic carbon content as measured by loss on ignition were also determined. The results provide a historical overview of the impact of industrialization in the Milwaukee area. Although highly variable, the concentration profile of PAHs show, in general, peaks in the 1950's through 1980's. The PAH concentrations have declined since then for most sediment cores. The current levels of total PAHs in most surface sediment samples range from 25 to 200 ppm. A few cores, some of which were collected in 1994, have an elevated PAH concentration at the surface. Toxicity of the surface sediments was evaluated by comparing with the benchmark values developed by the United States National Oceanic and Atmospheric Administration (NOAA). The most heavily contaminated area was found in the Kinnickinnic River between the Becher Street Bridge and the Wisconsin Wrecking Company Wharf. The highest total PAH concentration determined from seven vibra cores collected in this area ranges from 380 to 1000 ppm. The former Wisconsin Solvay Coke Company may have been a major point source of PAHs until the 1970's. Highway traffic and various industrial discharges also contribute to the sediment PAHs in this area.

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.

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 results of the first German moss monitoring programme to estimate heavy metal pollution in the Federal Republic of Germany were combined with other large-scale investigations carried out in Germany and then classified geographically in a new form. Using Monte Carlo assisted factor analysis, six factors indicating sources of pollution were identified from the sets of element data from the moss monitoring project (As, Cd, Cr, Cu, Fe, Ni, Pb, Ti, V, Zn) and the data sets for SO₂ and particulate. The geographic distribution patterns of the factor values showed the regions in which the various sources are to be found. By combining the data the primarily anthropogenic chromium concentrations of the mosses were compared with the mainly geogenic chromium concentrations of the stream sediments in the form of examples. After normalization, the transformed chromium concentrations were transferred to a map of the entire area using inverse distance weighting. Anthropogenic and geogenic influences are being discussed on the basis of the results.