Microorganisms isolated from soil are sources of known and new microorganisms and genetic material. This review examines general principles of soil bacterial biodiversity, limitations in sampling soils, and examples of bacterial diversity in chemically-contaminated soils. Both conventional and molecular methods used to assess microbial biodiversity in soils will be addressed as well as selected examples of the effects of organic and inorganic pollutants on soil microbial diversity.

The absorption of atmospheric radionuclides by soybean plants was experimentally studied using a radioactive multitracer consisting of radionuclides of Sc, Mn, Co, As, Se, Rb, Sr, Y, Eu, Gd, Yb, Hf, Re, and Ir. The soybean plants were cultivated in soil under no-rain conditions in a box containing air in which multitracer-absorbed cellulose particles were dispersed. The soil was covered with plastic film. After about one-month cultivation, the plants were harvested and washed with dilute HCl solution. The leaves, stems, and beans were subjected to γ-ray measurement. The radionuclides of As, Se, and Re were accumulated in the leaves, and those of Co, Se, and Rb were accumulated in the beans. Among them Se was accumulated to a large extent in the leaves and in the beans. Small amounts of the radionuclides of Co, Se, Rb and Re were found in the roots. Little absorption of these radionuclides into the soil occurred. These results indicate that various radionuclides in the atmosphere were absorbed through the soybean leaves and then transported to the seeds. These findings must be taken into consideration for a complete understanding of the system of uptake of radionuclides by the soybean plant.

In the practice of soil remediation, organoleptic observations such as the smell or the colour of contaminated soil play an important role when determining well-defined volumes of contaminated soil. A GIS is then used to combine quantitative measurements with such soft data. In this study general procedures concerning how to deal with this type of observations are presented. The procedures were applied to a former gas works site, which was contaminated with cyanide and polycyclic aromatic hydrocarbons in the Netherlands. The volume of contaminated soil was determined. Use of soft data reduced the uncertainty in the volume of contaminated soil with 4 to 16%.

Analysis of PCB, DDT, and chlordane contamination in selected finfish and shellfish species from estuarine and coastal marine waters of New Jersey (U.S.A.) indicates consistently highest organochlorine contaminant levels in samples from the north and northeast regions of the state in proximity to industrialized sites. Gas chromatographic analysis of tissue samples from three finfish species (bluefish, Pomatomus saltatrix; striped bass, Morone saxatilis; weakfish, Cynoscion regalis) and one shellfish species (blue crab, Callinectes sapidus) collected throughout the state during the 1986–1987 and 1988–1991 sampling periods revealed mean PCB, DDT, and chlordane concentrations ranging from 200–5, 380 µg g⁻¹ wet weight, 25.14–492.52 µg kg⁻¹ wet weight, and 5–106.44 µg kg⁻¹ wet weight, respectively. A major conclusion of this study is that some commercially and recreationally important finfish and shellfish species in New Jersey waters, especially those which are lipid-rich, have continued to accumulate PCBs, DDTs and chlordane from the environment long after restrictive regulations were first placed on their use in the United States during the 1970s. The greatest impact of organochlorine contamination is nearby urban centers, most notably Newark and New York City.

Acid deposition is considered to be a major environmental problem in China, but information about effects on soils and waters is scarce. To contribute to increased knowledge about the problem a small catchment (about 7 ha) in the outskirts of Guiyang, the provincial capital of Guizhou in south-western China, was instrumented for collection of precipitation, throughfall, soil water and stream water. In addition soil samples have been collected and analyzed for key properties. Median pH in the precipitation is 4.40 (quartiles: 4.19 and 4.77) and the median sulfate concentration 228 µeq/L (quartiles: 147 and 334 µeq/L). The dry deposition of both SO₂ and alkaline dust is considerable. The sum of wet deposition of sulfate and dry deposition of SO₂ has been estimated to about 8.5 gSm⁻²yr⁻¹. The total S-deposition may be somewhat higher due to dry deposition of sulfate and occult deposition. In soil water, SO₄ ²⁻ is the major anion, generally ranging from 300 to 2500 µeq/L in the different plots. Calcium is an important cation, but there is also a considerable contribution of aluminum from the soil. In some of the plots the concentrations of inorganic monomeric aluminum (Ali) are typically between 200 and 400 µm. Potential harmful levels of aluminum and/or high Ali/(Ca²⁺ + Mg²⁺) molar ratios occur in the catchment, but damages to vegetation have not yet been reported. In most cases exchangeable aluminum accounts for between 75 and 95% of the total effective cation exchange capacity (CECE) in the mineral soils. The aluminum chemistry cannot easily be explained by conventional models as the Gaines-Thomas ion-exchange equation or equilibrium with an Al(OH)₃ mineral phase. The stream water is generally less acidic and has considerably lower concentrations of aluminum than the soil water, even though quite acid events have been observed (pH < 4.4). The median pH values are 4.9 and 5.0 in the two first order streams and 6.3 in the dam at the lower boarder of the catchment.

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.