Two identical experimental subsurface-flow constructed wetlands were operated at relatively high organic loading rates (23 g COD m-² day-¹) for 4 months to evaluate their relative ability to remove either dissolved organic carbon (glucose, considered to be a readily biodegradable substrate) or particulate organic carbon (starch, considered to be a slowly biodegradable substrate). The systems were built using plastic containers (0.93 m long, 0.59 m wide and 0.52 m high) that were filled with an 0.35 m layer of wetted gravel (D₆₀ = 3.5 mm, uniformity coefficient Cu = D₆₀/D₁₀ = 1.7) and the water level was maintained at 0.05 m under the gravel surface to give a water depth of 0.30 m. The results indicated that there was no significant difference in COD removal between the two systems. Both systems generally had COD removal rates of over 90%, which is quite high if the heavy load applied is taken into account. The removal of ammonium was greater in the glucose-fed system (57%) in comparison with the starch-fed system (43%). Based on mass balance calculations and stoichiometric relationships, it was estimated that denitrification and sulphate reduction were minor pathways for the removal of organic matter. Indirect observations allowed to assume that methanogenesis made a highly significant contribution to the removal of organic matter.

Extensive measurements were made using an Aerodyne quantum cascade laser absorption spectrometer (QCLAS) to study the diurnal and seasonal cycles of NH₃ concentrations in Manchester city centre. Measurements made at rooftop levels showed traffic to be a significant source of NH₃ concentrations in the winter. This was illustrated by a bimodal diurnal cycle of NH₃ concentrations that was synchronized with traffic, and also by a correlation with NOx, a traffic related pollutant. These patterns were not observed during the summer, suggesting other sources become more important. Measurements were also made at street level during winter and summer, close to the traffic source. This time the contribution from traffic was also observed in the summer, albeit weaker. Enhanced NH₃ concentrations were often seen in winds from the southwest that could not be related to local sources, suggesting that ambient concentrations in the city are strongly influenced by sources outside the city. It is estimated that the total NH₃ emission from the city centre is between 0.7 and 2.3 t km-² year-¹.

Ammonia (NH₃) emission from nitrogen (N) fertilizers used in agriculture decreases N uptake by the crop and negatively impacts air quality. In order to better understand the factors influencing NH₃ emission from agriculture, this research was conducted with four major soils used for potato production: Biscayne Marl Soil (BMS, pH 7.27), and Krome Gravelly Loam (KGL, pH 7.69) from Florida; and Quincy Fine Sand (QFS, pH 6.65), and Warden Silt Loam (WSL, pH 6.46) from Washington. Potassium nitrate (KNO₃), ammonium nitrate (NH₄NO₃), ammonium sulfate ((NH₄)₂SO₄) or urea ((NH)₂CO) sources were evaluated for ammonia volatilization at 75 kg N ha-¹ rate. The soil water regime was maintained at either 20 or 80% of field capacity (FC), and incubated at 11, 20 or 29°C. Results indicated that NH₃ volatilization rate at 20% FC was 2 to 3-fold greater than that at 80% FC. The cumulative volatilization loss over 28 days ranged from 0.21% of N applied as NH₄NO₃ to 25.7% as (NH₄)₂SO₄. Results of this study demonstrate that NH₃ volatilization was accelerated at the low soil water regime. Moisture quotient (Q) is defined as a ratio of NH₃ emission rate at 20% FC to that at 80% FC both at the same temperature. The peak Q values of NH₃ volatilization were up to 20.8 for the BMS soil at 20°C, 112.9 for the KGL soil at 29°C, 19.0 for the QFS soil at 20°C, and 74.1 for the WSL soil at 29°C, respectively. Thus, maintaining a suitable soil water regime is important to minimize N-loss via NH₃ volatilization and to improve N uptake efficiency and air quality.

Runoff events were analysed in separated sewer systems in the town of Luxembourg. The relationships between Event Mean Concentrations of different pollutants and runoff patterns were evaluated. In addition, the inter-storm and intra-storm variability of the material transport were determined. Primarily, the variations in pollutant concentrations and loads are determined by the antecedent weather conditions. The presence of illicit sanitary inputs in one of the sewers produced a significant first flush effect as well as higher Event Mean Concentrations for pollutants. Furthermore, near the town of Trier 40 storms were analyzed in a small natural basin mainly influenced by runoff from a separated sewer system. Natural and artificial storm events were investigated in order to estimate the relationship between the pollutant sources in the channel and from the separated sewer system. Just like in the canalization of Luxembourg City the pollutant dynamics during natural storms are strongly influenced by pre-event hydrological conditions. The artificial storms behave differently. Despite little pre-rain, the maximum concentrations of toxic substances are comparatively low. A resuspension of sediment only occurs in the natural channel system, without the introduction of fines from the sewer system.

The impact of long-term dust pollution emitted from a cement plant on soil chemistry, and the concentrations of plant nutrients, lignin, cellulose and hemicellulose in the stemwood of 80–85-year-old Pinus sylvestris was investigated at different distances from the emission source. It was found that alkaline cement dust (pH 12.3–12.6) emissions for over 40 years resulted in an alkalisation (pH 6.7–7.9) of the polluted soil compared to a pH value of 3.8 in unpolluted soil. There were also nutrient imbalances in the soil, as well as certain disturbances in mineral nutrition processes and accumulation of nutrients in the tree stems. The average concentrations of K, Ca and Mg in stems were higher and those of N and P lower than in the unpolluted area. The lignin (L) content in stemwood increased, hemicellulose (Hc) decreased, while cellulose (Ce) did not change. A variation in the partitioning of L, Ce, Hc and nutrients between different sections of stems and between trees from different sample plots was found. L, Ce and Hc were not related to the internal K, Ca and Mg concentrations. Correlations were established between L, Ce, or Hc content and C content, and between L and Hc content in stem tissues. The contents of wood components were not related to N or P in the alkalised areas, but seemed to be more associated with P than with N. Alterations in the arbitrarily chosen ratio L/(Ce + Hc) indicated changes in wood quality, and a negative correlation with N/P was found in stem tissue in the polluted area, while positive correlations with N/Mg and Ca/Mg were found in the control area.

This study reports on the attachment preference of a faecally derived bacterium, Escherichia coli, to soil particles of defined size fractions. In a batch sorption experiment using a clay loam soil it was found that 35% of introduced E. coli cells were associated with soil particulates >2 μm diameter. Of this 35%, most of the E. coli (14%) were found to be associated with the size fraction 15-4 μm. This was attributed to the larger number of particles within this size range and its consequently greater surface area available for attachment. When results were normalised with respect to estimates of the surface area available for bacterial cell attachment to each size fraction, it was found that E. coli preferentially attached to those soil particles within the size range 30-16 μm. For soil particles >2 μm, E. coli showed at least 3.9 times more preference to associate with the 30-16 μm than any other fraction. We report that E. coli can associate with different soil particle size fractions in varying proportions and that this is likely to impact on the hydrological transfer of cells through soil and have clear implications for our wider understanding of the attachment dynamics of faecally derived bacteria in soils of different compositions.

The Bagmati River in Kathmandu valley, Nepal, was studied to understand the influence of human and geochemical processes on changes in river chemistry (nutrients, organic matter, and major cations and anions) along the drainage network. Population density appeared to drive variation in the chemistry of surface waters at 10 stations in the Bagmati River. For all constituents studied, concentrations increased with distance downstream and many parameters showed strong relationships with human population density adjacent to the river. The composition of river water suggests that sewage effluent entering the river has a major effect on water quality. Concentrations of most solutes were highest during summer and lower during the winter monsoon season. The contribution of chemical weathering processes to water quality of the Bagmati appears to be minor within the Kathmandu valley. Dominant cations and anions when expressed in equivalents per liter were [graphic removed] and [graphic removed] along the entire Bagmati drainage system. Ammonium contributed almost all nitrogen in the total dissolved nitrogen fraction and the concentration of nitrate was negligible, probably due to rapid denitrification and limited nitrification within the stream channel under conditions of relatively low oxygen. Decreases in sulfate along the stream channel may also be due to the reduction of sulfate to sulfide due to heavy organic matter loading. Water quality is unacceptable for any use and the whole ecosystem is severely affected due to human activities within the urban areas of the drainage basin.

Drainage water from agricultural fields with applied manure can degrade the bacterial quality of surface and groundwater. The impact of conventional tillage (CT) and zero tillage (ZT) practices on Escherichia coli (E.coli) discharge through artificially drained soils is not well understood. Consequently, two field trials were conducted during 2002–2004. The first trial involved fall applications of beef manure while the second involved spring applications of dairy manure. Both surface and subsurface drainage water were monitored in the first trial while only subsurface drainage water was monitored in the second. Under fall applied beef manure (trial 1), no differences (p > 0.05) were observed in E.coli concentrations (cfu/100 ml) in combined drainage water under both tillage systems. However, during 2003–2004, subsurface drainage water under ZT had higher E.coli concentrations and loads than drainage water under CT. When the combined (surface + subsurface) annual E.coli loads were considered, CT loads were greater than ZT during 2002–2003 with an opposite situation during 2003–2004. Overall, annual E.coli loads were similar under ZT (4.7 × 10¹⁰ cfu/ha) and CT (4.8 × 10¹⁰ cfu/ha). Spring dairy manure application (trial 2) produced significant (p > 0.03) tillage effect on E.coli loads in subsurface drainage water only during the second year. During the study period, ZT plots (1.55 × 10¹⁰ cfu/ha) discharged 5× more E.coli than CT (0.23 × 10¹⁰ cfu/ha). A longer duration of ZT practices resulted in higher subsurface flow volumes and subsequently greater loads of E.coli discharge in both trials.

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.

Field study at the Cervenohorske sedlo (1,013 m a.s.l.) (Hruby Jesenik Mountains, the Czech Republic, Central Europe) during 1999-2002 has been conducted in order to analyse the chemistry of rain/snow water using bulk and throughfall collector and fog/cloud water using modified passive Grunow collector. Fog water input to coniferous forest (Picea abies) was quantified using canopy balance method. For all samples pH, and the concentrations of [graphic removed] , Ca²⁺, K⁺, Mg²⁺, Na⁺, Cl-, [graphic removed] , and [graphic removed] were measured. The volume-weighted mean pH value varied from 4.92 to 5.43 in open bulk precipitation, from 4.30 to 4.71 in throughfall and from 4.66 to 5.23 in fog water. The fog droplets generally contain higher ion concentrations than rainwater. The related enrichment factors lie between 1.1 and 10.7 for the relevant species. The fog samples exhibit higher concentrations of [graphic removed] and [graphic removed] as compared to the bulk samples during 2000-2002. [graphic removed] are 5.7-10.7 times more concentrated in fog water and [graphic removed] are 3.4-7.2 times more concentrated in fog water. These differences may result from the height and characteristics of formation of the droplets. Based on canopy balance method, the annual fog water inputs were estimated to be 22 and 19% of rain and snow annual amounts in 1999 and 2000, respectively. For [graphic removed] , [graphic removed] , and [graphic removed] , the contribution of fog deposition in total (bulk + fog) deposition is estimated as 54, 47, and 42%, respectively.