The study uses measured and calculated data on airborne pollutants, particularly nitrogen (ranges between 28 to 43 kg N*ha-1*yr-1) and sulphur (10 to 18 kg SO4-S*ha-1*yr-1), in order to assess their long-term (1992 to 2005) effects on bryophytes at the UN-ECE Integrated Monitoring site 'Zöbelboden' in Austria. Bryophytes were used as reaction indicators on 20 epiphytic plots using the IM monitoring method and on 14 terrestrial plots using standardised photography. The plots were recorded in the years 1992, 1993, 1998, and 2004/2005. Most species remained stable in terms of their overall population size during the observed period, even though there were rapid turnover rates of a large percentage of species on all investigated plots. Only a few bryophytes (Hypnum cupressiforme, Leucodon sciuroides) responded unambiguously to N and S deposition. Nitrogen deposition had a weak but significant effect on the distribution of bryophyte communities. However, the time shifts in bryophyte communities did not depend on total deposition of N and S. Bryophytes show ambiguous response to airborne pollutants during 14 years of monitoring in a forest ecosystem.

The urban landscape is comprised of many land uses, none more intensively managed than turfgrass; however, quantification of nutrient losses from specific land uses within urban watersheds, specifically golf courses is limited. Nitrate (NO3-N) and dissolved reactive phosphorus (DRP) were measured on a golf course in Austin, TX, USA from April 1, 1998 to March 31, 2003. NO3-N and DRP concentrations measured in storm flow were significantly greater exiting the course compared to those entering the course. Significant differences were also measured in baseflow NO3-N concentrations. The measured loading from the course was 4.0 kg NO3-N ha 1 yr 1 (11% of applied) and 0.66 kg DRP ha 1 yr 1 (8% of applied). The resulting concentrations contributed by the course were 1.2 mg L 1 NO3-N and 0.2 mg L 1 DRP. At these levels, NO3-N poses minimal environmental risk. However, the DRP concentration is twice the recommended level to guard against eutrophication

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.

Levels of heavy metals (chromium, copper, lead and cadmium) in water and sediments of the lower Salado River (Argentina) are presented and compared to Canadian and Argentinian environmental standards. Measurement of metal levels was performed using atomic absorption spectroscopy. In order to interpret analytical results, one way ANOVA, hierarchical cluster analysis and correlations were used. Geoaccumulation Index was used as a measure of metal pollution in sediments. There were differences between the accumulation of metals in sediments and water and the control sampling site. Heavy metals, especially chromium, copper and lead, appear to be an important problem to these freshwater environments.

Industrialization and urbanization along the coastal population centers have brought great changes in the land cover and material fluxes from watersheds to receiving bays and estuaries. We have embarked a multiyear research project on “Watersheds Nutrient Loss and Eutrophication of Jiaozhou Bay” for the period of 2000 to 2004, funded by the Natural Science Foundation of China to examine human influence on the marine sector of ecosystem. Jiaozhou Bay, located in the southern part of Shandong Peninsula, was selected because of the existence of long-term hydrographic and meteorological records since the 1930s and recent observations on the marine ecological variables. We have made extensive and periodic measurements on the water movement, nutrients, phytoplankton, and microbe in water column and bottom sediments. Box and 3-dimensional hydrodynamic models were developed and utilized to understand the evolution of eutrophic status with time. It was found that primary productivity has suffered from silica depletion followed by phosphate, and the dominance of large phytoplankton has been replaced by small-size communities. These ecosystem changes were brought by the changes in the relative contribution among major pathways and concentrations, owing to the human activities in the watershed. Eight articles in this volume reported various aspects of the linkage between watershed human activities and ecosystem for the Jiaozhou Bay as the initial outcome of this project.

Critical loads have been successfully used within Europe in the development of effects-based policies for pollution abatement, including the Second Sulphur Protocol and the Protocol to abate acidification, eutrophication and ground-level ozone (CLRTAP, 1979). This success has encouraged the UK Environment Agency and Conservation Agencies to use the national critical load maps as a screening tool in assessing the threats from acidification and eutrophication to designated (Natura 2000) sites. The UK maps of critical loads are based on national-scale data sets appropriate for national-scale assessments, and were never intended for use at the site-specific level. Site-based assessments are often targeted at Special Areas of Conservation, a sub-set of the UK Natura 2000 sites. The spatial data available includes the boundaries of the sites but not the location of the designated features. Ancillary data is variable from one site to another; habitat types may be described in detail with cross-reference to classes of the National Vegetation Classification (NVC: Rodwell, 1991 et seq), but information available on soils and geology is generalised and has not been related to the habitats or species being protected. Hence it can be difficult to relate the individual sites to the national maps, even where appropriate to do so. This paper examines the underlying uncertainties in the national critical load maps showing how the maps could give misleading results if used for site-specific assessments. It also includes advice on how to determine when the national data may be appropriate as a policy-tool at the site-level.

The consequences of nitrogen (N) enrichment for terrestrial and freshwater ecosystems are of increasing concern in many areas due to continued or increasing high emission rates of reactive N. Within terrestrial ecosystems various conceptual frameworks and modelling approaches have been developed which have enhanced our understanding of the sequence of changes associated with increased N availability and help us predict their future impacts. Here, some recent findings are described and their implications for these conceptual frameworks and modelling approaches discussed. They are: (a) an early loss of plant species that are characteristic of low N conditions as N availability increases and a loss of species with high N retention efficiencies (so called N 'filters'), (b) suppression of microbial immobilisation of deposited [graphic removed] due to increased [graphic removed] availability in the early stages of N saturation, (c) the early onset of [graphic removed] leaching due to these changes (a and b above) in both plant and microbial functioning, (d) reduced sensitivity of vegetation to N additions in areas with high historical N deposition, (e) delayed changes in soil C:N changes due to increased net primary productivity and reduced decomposition of soil organic matter. Some suggestions of early indicators of N saturation are suggested (occurrence of mosses; [graphic removed] ratio in surface soils) which indicate either a shift in ecosystem function and/or structure.

BACKGROUND AND AIM: In non-eutrophicated freshwaters, humic substances (HS) pose chemical stresses on aquatic organisms and, hence, separating sensitive from less sensitive or even tolerant species. One of the stresses, identified so far, is the reduction of photosynthetic oxygen production and reduction in growth in freshwater macrophytes and algae. In a previous paper, it has been shown that even closely related coccal green algae responded differently upon identical stress by HS, which is consistent with the hypothesis above. Due to their much simpler cellular ultrastructure, cyanobacteria are supposed to be more sensitive to HS exposure than eukaryote should be. One coccal green algal species (Desmodesmus communis) and one cyanobacterium (Chroococcus minutus) were exposed to four natural organic matter (NOM) isolates. One NOM has been isolated from a brown water lake (Schwarzer See) in Brandenburg State; three were obtained from a comprehensive Scandinavian NOM research project and originated from Norway (Birkenes), Finland (Hietajärvi), and Sweden (Svartberget). METHODS: Cultures of D. communis and C. minutus were obtained from the Culture Collection of Algae, Göttingen, and maintained in a common medium. The cultures were non-axenic. The algae and cyanobacteria were exposed under identical conditions to environmentally realistic NOM concentrations. Cell numbers were counted microscopically in Neugebauer cuvettes in triplicates. To avoid limitation by nutrient depletion, the experiments were terminated after 14 to 15 days. Until culture day 12, no growth limitation has been observed in the controls. RESULTS: All NOM isolates modulated the growth of the algae and cyanobacteria. During the early culture days, there was a slight growth promotion with the coccal green alga and to a much lesser degree with the cyanobacterium. Yet, the major effect were significant reductions in cell yield in both primary producer cultures. C. minutus was much more affected than D. communis. This applies particularly to the three tested Scandinavian NOM isolates, which were effective at concentrations even below 1 mg L-1 DOC. DISCUSSION: The growth promoting effect may be due to an increase in bioavailability of some trace nutrients in the presence of NOM, the release of some growth promoting substances by microbial or photochemical processing of the NOM, and/or a hormetic effect. The growth reducing effect can be explained as a herbicide-like mode of action that affects the photosystem II most prevalent by blocking the electron transport chain, absorption of electrons, or production of an internal oxidative stress after processing the bioconcentrated HS. Furthermore, it may be postulated that also phototoxicity of these HS in the algal cells contributes to the overall toxicity; however, experimental evidence is lacking so far. CONCLUSIONS: Upon exposure to HS, cyanobacteria appear to be much more sensitive than coccal green algae and respond in growth reduction. This high sensitivity of cyanobacteria to HS may explain phytoplankton patterns in the field. Eutrophic, humic-rich lakes do not support the cyanobacterial blooms characteristic of eutrophic, but humic-poor lakes. In the humic-rich systems, raphidophytes or, less frequent, specific coccal greens are more common. Obviously, cyanobacteria appear to be unable to make advantage of their accessory pigments (phycocyanin) to exploit the reddish light prevailing in humic-rich lakes. RECOMMENDATION: At present, no effective structure can be figured out which may be responsible for the adverse effect on the cyanobacterial species. It is reserved to future research whether or not HS may be applied more specifically (for instance, with elevated moieties of the effective structures) as a natural geochemical to combat cyanobacterial blooms.