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.

The bioaccumulation and toxicity of zinc in Spirogyra fluviatilis Hilse, from two populations in the River Seyhan, Adana, Turkey, were examined in laboratory flowing-water channels. Plants were subjected to zinc concentrations ranging from 0 to 4.0 mg L⁻¹ at current velocities of 25–35 cm s⁻¹ for up to 3 h. There was little difference in zinc bioaccumulation between Spirogyra from the site showing mild organic pollution and that from the site subjected to considerable inputs from urban and motorway runoff. Uptake of zinc increased with increasing concentration in the test solution and was linear and proportional up to 0.5 mg L⁻¹. Cellular damage was evident in Spirogyra subjected to 0.5 mg L⁻¹ zinc, and increased with increasing zinc concentration.

Phosphine is a toxic agent and part of the phosphorus cycle. A hitherto unknown formation mechanism for phosphine in the environment was investigated. When iron samples containing iron phosphide were incubated in corrosive aquatic media affected by microbial metabolites, phosphine was liberated and measured by gas chromatography. Iron liberates phosphine especially in anoxic aquatic media under the influence of sulfide and an acidic pH. A phosphine-forming mechanism is suggested: Phosphate, an impurity of iron containing minerals, is reduced abioticly to iron phosphide. When iron is exposed to the environment (e.g. as outdoor equipment, scrap, contamination in iron milled food or as iron meteorites) and corrodes, the iron phosphide present in the iron is suspended in the medium and can hydrolyze to phosphine. Phosphine can accumulate to measurable quantities in anoxic microbial media, accelerating corrosion and preserving the phosphine formed from oxidation.