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.

A spatially extensive geochemical data set of stream water and bed sediment composition across the Tamar catchment in south-west England was analysed to identify the key bed sediment properties that control the in-stream dissolved reactive phosphorus (DRP) concentrations during baseflow conditions. Linear regression analysis of the streamwater DRP concentrations and the distribution coefficient K d for DRP revealed that the former is positively correlated with total SiO₂ and Al₂O₃, and negatively correlated with K₂O. The primary control on these major element distributions is the dominant bedrock geology. The data suggest that streamwater DRP concentrations are mainly controlled by adsorption to clay minerals. Where P concentrations in streamwater were considerably elevated by inputs from point sources, DRP concentrations are also controlled by precipitation of hydroxyapatite.

Cootes Paradise is a coastal wetland, adjacent to Hamilton Harbour at the western tip of Lake Ontario. The marsh has been considerably degraded due to the excessive sediment and nutrient input from sewage treatment plants (STPs), marsh tributaries and Combined Sewer Overflows (CSOs). Although there has been reduction in nutrient loadings from external sources, high nutrient levels, and a prolific algal growth remain a problem in Cootes Paradise. To assess the importance of external versus internal nutrient loadings to the marsh, nutrient fluxes from sediments were estimated using porewater profiles at three locations from 2001 and five additional sites from 2002. The fluxes varied between 0.27 and 5.25 mg P m-² day-¹, with sites receiving outfalls of STP and CSO having highest fluxes (~5 mg P m-² day-¹). Mean phosphorus release rate of 2.02 mg P m-² day-¹ was calculated from the spatial distribution of the non-apatite inorganic phosphorus (NAI-P) in sediments, employing a relationship between the NAI-P and P fluxes. The results confirm that sediment P geochemistry is important in regulating the P pool in porewater which, consequently, governs the P fluxes from sediments.

Deposition and storage of fine sediment on channel beds represents an important component of a catchment's sediment budget and can have important implications for sediment-associated P fluxes, due to storage and remobilisation, and for P concentrations through water-sediment interactions. Spatial and temporal variations in P content and storage in fine bed sediment have been studied in two UK lowland catchments, the Rivers Frome and Piddle in Dorset. Fine bed sediment was sampled in representative reaches on a bi-monthly basis using a re-suspension cylinder, and the resulting samples were analysed for total P, a range of P fractions and particle size. The results demonstrate significant spatial and temporal variability in PP concentrations and storage, with maximum and minimum P concentrations and storage occurring in late summer and winter, respectively. Temporal variations in concentrations reflect residence times of the sediment and ambient P concentrations, while variations in storage are mainly due to hydrological regimes. Spatial variations reflect catchment characteristics, the location of inputs and local variations in hydrological and channel bed conditions.

Danish rivers carry >50% of the phosphorus (P) transport as particulate P (PP). In five of six rivers sampled in November 1998 iron-bound P made up > 59% of PP and loosely adsorbed P ranged between 2% and 13%. This fraction could potentially be released in 14[per thousand] seawater. The behaviour of dissolved and particulate P fractions was studied during seven month in a 2 km long estuary with low freshwater retention time and low tidal range. The river carried ~10% of PP as loosely adsorbed P but increased concentrations of dissolved inorganic P (DIP) relative to the estuarine mixing line was only observed in the summer month with low freshwater flow and was more likely due to DIP release from the bottom sediment. Instead estuarine particles were always enriched with oxidized iron (ox.Fe) and iron-bound P as well as loosely adsorbed P and during May-September this coincided with increasing concentration of PP in estuary. We suggest that flocculation of ox.Fe and adsorption of DIP onto the particles with subsequent transport seawards is a major loss process for P during the summer month. During winter month where 85% of the run-off occurs the dominant process in the estuary is sedimentation of larger particles, however, a comparison of river particles with surface sediment clearly reveals that most PP is mobilized again from the bottom sediments.

One of the methods to diminish the internal phosphorus (P) loading is inactivation of P by aluminum (Al). After addition of Al to lake water an Al(OH)₃ floc is formed, which settles to the bottom and initially form a lid on the sediment surface. The effects of Chironomus plumosus larvae on sediment nutrient fluxes and P binding-sites in the sediment after addition of Al were tested. C. plumosus larvae were added to sediment cores in which sediment-water fluxes of nutrients were measured four times. After one month, the sediment was sectioned with depth and P fractions were measured by sequential chemical extraction. The chironomids created burrows through the Al layer which caused a significantly increased efflux of P from the Al treated sediment, because the P had only limited contact to the added Al. The chironomids also affected the P fractions in the sediment by their bioturbating activity. Thus, they caused increased Al concentrations in the upper part of the Al treated sediment. This created an enhanced contact between Al and P in the upper 7 cm of the sediment and, as a result, an increased binding of P to Al and a lowered porewater P. The DIP efflux is therefore expected to be lowered after the initial phase. Al had no effects on the nitrogen fluxes, but the chironomids enhanced the [graphic removed] release, and decreased the [graphic removed] release or increased the [graphic removed] uptake by the sediments.

During spring of 2005, referent monitoring of the chemical quality of surface waters and sediments in some protected areas in Vojvodina (Serbia) was conducted as a supplement to the Regular monitoring program. The aim of the study was to establish the chemical quality of surface waters and sediments regarding nutrient content. It is shown that the water quality satisfies the criteria of the 1st/2nd class according to our legislation, with the exception of the Ludos location, which showed a contamination with nitrogen matter in water and sediments. With regard to the contamination of water with phosphorus, almost all locations may be considered as potentially problematic.

Within the pollutant analysis in sediments the total organic carbon (TOC) content is determined, as well as nutrients such as nitrogen and phosphorus. In addition to this form carbon may be present as elemental or inorganic ones, as the crucial issue for sample preparation. Total phosphorus content was determined after sample digestion with sulphuric and perchloric acid. Organic nitrogen values were determined according the Kjeldahl method. Concentrations of TC, TOC, TIC, total P, organic N and total N in river Tisza sediment samples from sites Martonos, Novi Becej and Titel during 2004 and 2005 were presented.