In industrial barrens adjacent to a nickel-copper smelter at Monchegorsk, the Kola Peninsula, root colonisation in Deschampsia flexuosa by arbuscular mycorrhizal (AM)-type of hyphae was lower than in unpolluted forests (60.9 vs. 80.4%), while Olpidium-colonisation showed a marginally significant decline, and dark septate endophytic (DSE) hyphal colonisation was not affected. We detected an interactive effect of pollution and a neighbouring tree on DSE hyphal colonisation: at the highly polluted sites, colonisation was lower in D. flexuosa growing near trees, whereas at sites with low pollution the presence of the neighbouring tree had no effect on colonisation. High numbers of intracellular DSE sclerotia in the industrial barrens (13.3 vs. 3.4%) may indicate a survial strategy in an unfavourable environment and a dispersal strategy into a more favourable environment. While lower root colonisation by AM fungi has been also earlier reported in graminoids for heavy metal contamination, the results on other ubiquitous fungi colonising D. flexuosa roots are more novel. Severe pollution decreased root colonisation by some fungal groups; neighbouring trees decreased root colonisation by dark septate endophytic fungi in highly polluted sites.

Recent studies have demonstrated that natural abundance 15N can be a useful tool for assessing nitrogen saturation, because as nitrification and nitrate loss increase, δ15N of foliage and soil also increases. We measured foliar δ15N at 11 high-elevation spruce-fir stands along an N deposition gradient in 1987-1988 and at seven paired northern hardwood and spruce-fir stands in 1999. In 1999, foliar δ15N increased from -5.2 to -0.7[per thousand] with increasing N deposition from Maine to NY. Foliar δ15N decreased between 1987-1988 and 1999, while foliar %N increased and foliar C:N decreased at most sites. Foliar δ15N was strongly correlated with N deposition, and was also positively correlated with net nitrification potential and negatively correlated with soil C:N ratio. Although the increase in foliar %N is consistent with a progression towards N saturation, other results of this study suggest that, in 1999, these stands were further from N saturation than in 1987-1988. Foliar δ15N increased with increasing N deposition from Maine to NY, but decreased between 1987-1988 and 1999

Concern regarding the impacts of continued nitrogen and sulfur deposition on ecosystem health has prompted the development of critical acid load assessments for forest soils. A critical acid load is a quantitative estimate of exposure to one or more pollutants at or above which harmful acidification-related effects on sensitive elements of the environment occur. A pollutant load in excess of a critical acid load is termed exceedance. This study combined a simple mass balance equation with national-scale databases to estimate critical acid load and exceedance for forest soils at a 1-km2 spatial resolution across the conterminous US. This study estimated that about 15% of US forest soils are in exceedance of their critical acid load by more than 250 eq ha-1 yr-1, including much of New England and West Virginia. Very few areas of exceedance were predicted in the western US. This simple mass balance equation estimated that 17% of US forest soils exceed their critical acid load by more than 250 eq ha-1 yr-1, and these areas are predominantly located in the northeastern US.

Simple mass balance equations (SMBE) of critical acid loads (CAL) in forest soil were developed to assess potential risks of air pollutants to ecosystems. However, to apply SMBE reliably at large scales, SMBE must be tested for adequacy and uncertainty. Our goal was to provide a detailed analysis of uncertainty in SMBE so that sound strategies for scaling up CAL estimates to the national scale could be developed. Specifically, we wanted to quantify CAL uncertainty under natural variability in 17 model parameters, and determine their relative contributions in predicting CAL. Results indicated that uncertainty in CAL came primarily from components of base cation weathering (BCw; 49%) and acid neutralizing capacity (46%), whereas the most critical parameters were BCw base rate (62%), soil depth (20%), and soil temperature (11%). Thus, improvements in estimates of these factors are crucial to reducing uncertainty and successfully scaling up SMBE for national assessments of CAL.

Many air pollutants and greenhouse gases have common sources, contribute to radiative balance, interact in the atmosphere, and affect ecosystems. The impacts on forest ecosystems have been traditionally treated separately for air pollution and climate change. However, the combined effects may significantly differ from a sum of separate effects. We review the links between air pollution and climate change and their interactive effects on northern hemisphere forests. A simultaneous addressing of the air pollution and climate change effects on forests may result in more effective research, management and monitoring as well as better integration of local, national and global environmental policies. Simultaneous addressing air pollution and climate change effects on forests is an opportunity for capturing synergies in future research and monitoring.

The effects of soil processes, related to the oxidation of sulphide sediments, on heavy metal concentrations in the soil and soil solution were investigated in a Norway spruce stand on a fine-textured, acidic soil rich in sulphates located on the isostatic land-uplift western coast of Finland. The age of the soil is ca. 300–400 years, and the soil texture is silt and till. The chemical properties of the soil and soil solution clearly reflected the formation of acid sulphate (AS) soil. Compared to background reference values for podzolic coniferous forest soil, the pH of the soil solution in the mineral soil (20–40 cm depth) was very low, and the Al, Fe and S concentrations extremely high. The Zn and Ni concentrations in the soil solution were also strongly elevated, and similar to the concentrations reported close to anthropogenic heavy-metal emission sources. The concentrations of Cd and Cu were also frequently elevated. In contrast, the acidity and metal concentrations of the soil solution sampled in the organic layer were not elevated. Similarly, exchangeable Zn and Ni concentrations were also elevated in the mineral soil, but not in the organic layer. Because Norway spruce has a very superficial rooting system and the zone with exceptionally high metal concentrations did not extend up to the topmost soil layers, sulphide-oxidation derived soil acidification is not likely to pose a serious threat to forest ecosystems growing on this type of site. Despite the elevated concentrations of protons and many metals in the mineral soil and soil solution (20–40 cm), the nutrient status of the spruce stand was satisfactory and the general health of the stand has been reported to be relatively good.

The effects of harvesting on the long-term mass balances of calcium (Ca), magnesium (Mg) and potassium (K) were evaluated on a regional level in Sweden. A new high-resolution weathering database was used together with estimates of total deposition, losses through harvest and leaching. Estimates were made for pine and spruce separately and for two harvesting intensity scenarios: stem harvesting and whole-tree harvesting. The mass balance calculations showed net losses of Ca and Mg in almost the whole country for both scenarios. The losses were smaller for pine than for spruce. The K balances were mainly positive for pine but negative for spruce. Leaching was a main factor in the mass balances, especially for Ca and Mg. Whole-tree harvesting in spruce forests led to substantially higher net losses of K and Ca than stem harvesting, according to the calculations. In the whole-tree harvesting scenario in spruce forests the estimated yearly net losses of Ca, Mg and K corresponded to at least 5%, 8% and 3% of the pools of exchangeable base cations, respectively, at 25% of the analysed sites. If losses of this magnitude continue the depletion of the pools of Ca, Mg and K may lead to very low base saturation of the soils, possibly accompanied by negative effects on soil fertility, runoff water quality, tree vitality and tree growth within a forest rotation in parts of Sweden. Avoiding whole-tree harvesting can improve the situation substantially for K, but the losses of Ca and Mg will still be significant.

In order to restore the forest ecosystem in the vicinity of an industrial park, Ulsan, southeastern Korea, which has been heavily acidified by air pollution, a preliminary experiment by applying tolerant plants selected through several procedures, and dolomite and sewage sludge as soil ameliorators was carried out. Furthermore, a restoration based on the results was executed and the effects were evaluated based on the creation of safe sites, where new species can establish: regeneration of the forest with species similar in composition to the natural vegetation of native forests that are distant from the industrial park; increase in species diversity. In a preliminary study, the necessity of soil amelioration was diagnosed. Quercus serrata, Alnus firma and Ligustrum japonicum, which represent for tree, subtree, and shrub layers of vegetation in this region, were used as sample plants. Dolomite, sludge, and a mixture of both materials were applied as soil ameliorators. Bare ground (BG), and two grasslands dominated by forbs (GF) and grass (GG), respectively were designated as experimental plots based on a vegetation map of the corresponding area. BG and GF plots, which have lower organic matter contents, increased the growth of sample plants in response to soil amelioration, whereas that with higher contents, GG plot, did not show this response. The result suggests that necessity of soil amelioration depends on site quality. The effects of soil amelioration depended also on the sample plants. This difference is due to an ecological property of A. firma, which can fix atmospheric nitrogen through a symbiotic relationship with actinomycetic fungi. This result implies that this alder could be used as a substitute for soil ameliorators in restoration plan of this area. The height and standing crop of undergrowth, which forms dense grass mat and thereby impedes establishment of new plants, decreased in the restored stands. Such a decrease in the height and biomass of undergrowth could be recognized as providing safe sites, in which the other plants can invade, by removing the dense carpet formed by Miscanthus sinensis. The results of stand ordination showed a progression of the former bare grounds to either M. sinensis (GG) or Pueraria thunbergiana (GF) stands, suggesting a natural recovery through succession toward the stands dominated by both plants. But the change was not progressed beyond the grassland stage. Active restoration practice, which was carried out by applying tolerant plants, however, led to a change toward species composition similar to the natural vegetation before devastation. Furthermore, restored stands reflected the restoration effect by showing higher diversity than the stands in the degraded state. These results showed that the restorative treatment carried out by introducing tolerant plants functioned toward increasing both biological integrity and ecological stability and thereby could meet the restoration goal.

Manganese (Mn) contamination of drinking water may cause aesthetic and human health problems when concentrations exceed 50 and 500 μg l⁻¹, respectively. In the UK, the majority of Mn-related drinking water supply failures originate from unpolluted upland catchments. The source of Mn is therefore soil, but the exact mechanisms by which it is mobilised into surface waters remain unknown. Elevated Mn concentrations in surface waters have been associated with the rewetting of dried upland soils and with conifer afforestation. We investigated these hypotheses in a laboratory experiment involving the drying and rewetting of intact soil cores (1,900 cm³ volume) of horizons of four representative soil type-land use combinations from an upland water supply catchment in southwest Scotland. Although no statistically significant effect of land use or soil type was detected on Mn concentrations in soil water, Mn release occurred from three soil horizons upon rewetting. Soil water Mn concentrations in the moorland histosol H2 (10–30 cm), the histic podzol H and Eh horizons increased from means of 5.8, 6.2 and 0.6 μg l⁻¹ prior to rewetting to maxima of 90, 76 and 174 μg l⁻¹ after rewetting, respectively. The properties of these three horizons indicate that Mn release is favoured from soil horizons containing a mixture of organic and mineral material. Mineral material provides a source of Mn, but relatively high soil organic matter content is required to facilitate mobilisation. The results can be used alongside soil information to identify catchments at risk of elevated Mn concentrations in water supplies.

Methylation and demethylation of arsenic may change substantially the toxicity and mobility of arsenic in soils. Little is known about demethylation of organic arsenic species in organic soils. We incubated dimethylarsinic acid (DMA) and arsenobetaine (AsB) in soils and aqueous soil extracts from a forest floor and fen, in order to investigate demethylation processes. Incubations were conducted at 5°C in the dark under oxic or anoxic conditions. Arsenobetaine demethylated rapidly in all soil extracts with half-lives of 3.6–12 days, estimated from first order kinetic. Demethylation of DMA was relatively slow with half-lives of 187 and 46 days in the forest floor extracts and oxic fen extracts, respectively. In comparison, DMA was stable for 100 days in anoxic fen extracts. The apparent half-lives were much shorter in soils for DMA (1.3–12.6 days) and AsB (0.5–1.9 days) than in soil extracts, suggesting also irreversible AsB and DMA adsorption to soils beside demethylation. An unknown arsenic species and DMA were detected as metabolites of AsB demethylation. The results indicate rapid demethylation of AsB probably via the pathway AsB → Dimethylarsenoylacetate → DMA, followed up by slow demethylation of DMA → monomethylarsonic acid → inorganic As species.