Steady-state models for the prediction of P retention coefficient (R) in lakes were evaluated using data from 93 natural lakes and 119 reservoirs situated in the temperate zone. Most of the already existing models predicted R relatively successfully in lakes while it was seriously under-estimated in reservoirs. A statistical analysis indicated the main causes of differences in R between lakes and reservoirs: (a) distinct relationships between P sedimentation coefficient, depth, and water residence time; (b) existence of significant inflow-outflow P concentration gradients in reservoirs. Two new models of different complexity were developed for estimating R in reservoirs: [graphic removed] , where τ is water residence time (year), was derived from the Vollenweider/Larsen and Mercier model by adding a calibrated parameter accounting for spatial P non-homogeneity in the water body, and is applicable for reservoirs but not lakes, and [graphic removed] , where [Pin] is volume-weighted P concentration in all inputs to the water body (μg l-¹), was obtained by re-calibrating the OECD general equation, and is generally applicable for both lakes and reservoirs. These optimised models yield unbiased estimates over a large range of reservoir types.

In Hypericumspecies some specimens have been found to display higher levels of the toxic heavy metal Cd than the proposed guide value of 0.5mgkg. Plant and soil samples from various regions in Eastern Austria were collected to study the variability in the Cd content of the herbs and relate it to selected soil properties and soil micronutrient contents. The soils contained between 0.01 and 0.44mgkg-¹Cd in the dry soil. Altogether about 7% of the collected plant samples exceeded 0.5mgkg-¹Cd of dry shoots, the proposed guide value for the drug Herba Hyperici. Plants low in Cd were found on sites in the Alpenvorland, the Hainburger Berge, the Eastern Viennese Basin and the Northern Limestone Alps where the levels did not exceed 0.3mgkg-¹Cd of dry shoots. Higher Cd levels in the plants were present in material from the Waldviertel, the Southern Wienerwald and the Semmering region where often bioaccumulation factors for Cd above 1 could be calculated. In these regions the soil pH and carbonate content was somewhat lower than in other regions whereas the soil organic carbon varied greatly. In the Waldviertel some plants from a field were somewhat higher in Cd than nearby plants from the natural vegetation. In a regression analysis, the soil pH, soil organic carbon and soil Cd content were the main factors influencing Cd accumulation in the plant shoots.

Although lead (Pb) emissions have dropped drastically with the phase-out of tetra-ethyl lead (TEL) as a fuel additive, Pb deposited along highway corridors continues to be of concern because of its toxicity. This paper provides comprehensive data on the extent and distribution of Pb in roadside soils, Pb interaction with soils as a function of soil composition, the retention capacity of soil based on batch adsorption tests, the retention mechanism of Pb using selective sequential extraction, the potential for mobility using batch desorption tests with simulated rain and winter road salt, and column leach tests. Highway soils on high-traffic sections near Burnaby, Canada were found to have Pb accumulations up to 1628mg/kg soil. Contamination was mainly in the top 0.3m, with concentrations rapidly decreasing to the background level at a depth of 0.6m. The top layer contained more organic material and had a high adsorption capacity. Highway soils were found to have 3-10 times higher Pb adsorption capacities than the amount currently deposited. Selective sequential extraction indicated low exchangeable Pb in highway soils. Batch desorption tests with leaching solutions of H₂O (pH 5.5), HNO₃ solution (pH 4.0) and aqueous NaCl solution (0.17M) indicate low likelihood of significant leaching. Selective sequential extraction, leachate extraction and desorption tests show that Pb has limited mobility in highway soil.

The adsorption and degradation of chlorobenzene on partially modified organoclays and by the autochthonous microorganism Rhodococcus B528 were studied by means of the batch technique. Organoclays were prepared from Na-montmorillonite (MM) by using dodecyltrimethylammonium (C₁₂) and dioctadecyldimethylammonium (2C₁₈) bromides. The degree of modification was 35 (2C₁₈-35-MM) and 89% (C₁₂-89-MM) of the cation exchange capacity of MM. The adsorption experiments were carried out using headspace GC. The intercalation of chlorobenzene into the interlayers of organo-MM was detected by X-ray diffraction. The adsorption isotherms found were of the S1 type indicating a cooperative effect. Chlorobenzene showed a higher affinity for 2C₁₈-35-MM than C₁₂-89-MM, which could not only be explained by the organic carbon content. The comparison with 2,4-dichlorophenol adsorption has implied that for the studied systems the different adsorption mechanisms are primarily governed by the different molecular properties and not by the type of absorbent. The presence of 2C₁₈-35-MM caused no negative effect on the investigated microorganisms and complete biodegradation of chlorobenzene was achieved without desorption limitation for growth, demonstrating the applicability of partially modified organoclays for bioremediation.

Nutrient spiralling measurements were conducted in Lyrebird Creek, a forested stream in the Dandenong Ranges, Victoria, Australia. Spiralling indices from several nutrient ([graphic removed] , [graphic removed]) enrichment experiments were correlated with seasonal variation in factors thought to control nutrient uptake, i.e., temperature, light and algal biomass. It was hypothesized that nutrient uptake would be higher in summer as increased temperatures would promote both biotic and abiotic processes and higher light levels in summer would stimulate photosynthesis. However, results did not support this hypothesis. Uptake length for [graphic removed] and [graphic removed] and uptake velocity were not correlated with chlorophyll-a, light or temperature (r ² < 0.30, P > 0.1) despite the seasonality of these biophysical factors (r ² > 0.42, P < 0.02). Lyrebird Creek might had no seasonal trend in nutrient uptake and/or nutrient spiraling measurements only appears suitable for contrasting streams with large differences in biophysical factors that supports biotic and abiotic nutrient processing. In addition, small errors in measuring a nutrient concentration can result in a large range in the estimated S w and increased difficulty in determining significant differences in nutrient spiralling indices.

Atmospherically deposited lead in the upper layer of the heavily eroded peatlands of the Peak District, southern Pennines, UK, reaches concentrations in excess of 1,000 mg kg-¹. Erosion of the upper peat layer in this region is releasing lead, associated with eroded peat particles, into the fluvial system. Understanding the process mechanisms that control dissolved lead concentrations in contaminated peatland streams is vital for understanding lead cycling and transport in peatland streams. Many headwater streams of the southern Pennines recharge drinking water reservoirs. Measurements in the Upper North Grain (UNG) study catchment show that mean sediment-associated and dissolved lead concentrations are 102 ± 39.4 mg kg-¹ and 5.73 ± 2.16 μg l-¹, respectively. Experimental evidence demonstrates that lead can desorb from suspended sediments, composed of contaminated peat, into stream waters. In-stream processing could therefore account for the elevated dissolved lead concentrations in the fluvial system of UNG.

The overall objective of this research was to develop a reliable, robust, and maintenance-free passive system for biological denitrification in on-site wastewater treatment systems. The process relies on sulfur oxidizing denitrifying bacteria in upflow packed bioreactors. Since this process consumes alkalinity, it is necessary to add a solid-phase buffer that can scavenge the H⁺ as it is generated by the biologically-mediated reaction and arrest the drop in the pH value. This study investigated the use of limestone, marble chips and crushed oyster shell as solid-phase buffers that provide alkalinity. Two bench-scale upflow column reactors and two field-scale bioreactors were constructed and packed with sulfur pellets and an alkalinity source. The pilot scale bioreactors (~200 L each) were installed at the Massachusetts Alternative Septic System Test Center (MASSTC) in Sandwich, MA. The pilot-scale bioreactors performed better when oyster shell was used as the solid-phase buffer vis-à-vis marble chips. In both (pilot-scale and laboratory-scale) systems, denitrification rates were high with the effluent NO₃ - --N concentration consistently below 8 mg/L.

In August of 2003 a severe wildfire burnt the majority of Fishtrap Creek, a 170 km² catchment in central British Columbia, Canada. The objective of this study was to determine the short-term (15-month) influence of the wildfire on the amount and composition of fine sediment delivery and retention in the system and to compare it to a similar unburnt catchment. In the spring of 2004 automatic water samplers were installed at a gauging site on Fishtrap Creek to collect suspended sediments from the snowmelt runoff and gravel traps were deployed on the channel bed surface to collect composite samples of suspended fine sediment. Jamieson, the reference creek, exhibits similar geology and pre-burn vegetation and was sampled in the same manner for comparison. Composite suspended sediment collected in the traps was removed from the streams in mid-summer and early September. Quantitative estimates of the amount and particle size structure of the naturally stored fine sediment in, and on, the gravel creekbed were obtained in pre-melt, mid and late-summer conditions. Estimates of suspended sediment yields indicated that while the burnt system delivered 66% more material per unit area, the total seasonal suspended sediment yield was low (855 kg km-²) compared to other fire-disturbed systems. While the burnt catchment was primed to deliver sediment, the hydrologic drivers were not of sufficient magnitude to generate a substantial response, suggesting that in this first post-fire year the system was transport-limited, not supply-limited. Differences were noted in the spatial and seasonal composition of the <500 more OM% composite suspended sedimentswith the burnt catchment having significantly (P<=0.05) more OM%. Seasonally a significant increase of OM% in late summer samples was associated with instream biofilms and possible delivery of black carbon. The system's post-fire response was not geomorphically substantial but significant biological differences were noted in the short-term.

This paper describes a study examining the potential of mineral magnetic, geochemical and organic properties to determine if a 2003 wildfire in a catchment in British Columbia, Canada, caused a change in the sources of the suspended sediment transported in the channel relative to a nearby unburnt (reference) catchment. The results show that some of the properties offer the potential to determine sediment sources in the unburnt catchment. However, the 2003 wildfire modified the concentrations of some properties and this can either compromise or enhance their ability as tracers in the burnt catchment. At present, the source tracing results are inconclusive. This has implications for the use of certain properties as fingerprints and raises important issues about approaches to sediment source identification.

We estimated the total inorganic fluxes of nitrogen (N), sulfur (S), chloride (Cl-, sodium (Na⁺, calcium (Ca²⁺, magnesium (Mg²⁺, potassium (K⁺ and hydronium (H⁺. The resistance deposition algorithm that is programmed as part of the CALMET/CALPUFF modeling system was used to generate spatially-distributed deposition velocities, which were then combined with measurements of urban and rural concentrations of gas and particle species to obtain dry deposition rates. Wet deposition rates for each species were determined from rainfall concentrations and amounts available from the National Acid Deposition Program (NADP) monitoring network databases. The estimated total inorganic nitrogen deposition to the Tampa Bay watershed (excluding Tampa Bay) was 17 kg-N ha-¹ yr-¹ or 9,700 metric tons yr-¹, and the ratio of dry to wet deposition rates was ~2.3 for inorganic nitrogen. The largest contributors to the total N flux were ammonia (NH₃ and nitrogen oxides (NO x at 4.6 kg-N ha-¹ yr-¹ and 5.1 kg-N ha-¹ yr-¹, respectively. Averaged wet deposition rates were 2.3 and 2.7 kg-N ha-¹ yr-¹ for NH₄ ⁺ and NO₃ -, respectively.