This paper presents an improved version of a general, process-based mass-balance model (LakeMab/LEEDS) for phosphorus in entire lakes (the ecosystem scale). The focus in this work is set on the boundary conditions, i.e., the domain of the model, and critical tests to reveal those boundary conditions using data from a wide limnological range. The basic structure of the model, and many key equations have been presented and motivated before, but this work presents several new developments. The LakeMab-model is based on ordinary differential equations regulating inflow, outflow and internal fluxes and the temporal resolution is one month to reflect seasonal variations. The model consists of four compartments: surface water, deep water, sediment on accumulation areas and sediment on areas of erosion and transportation. The separation between the surface-water layer and the deep-water layer is not done from water temperature data, but from sedimentological criteria (from the theoretical wave base, which regulates where wind/wave-induced resuspension of fine sediments occurs). There are algorithms for processes regulating internal fluxes and internal loading, e.g., sedimentation, resuspension, diffusion, mixing and burial. Critical model tests were made using data from 41 lakes of very different character and the results show that the model could predict mean monthly TP-concentrations in water very well (generally within the uncertainty bands given by the empirical data). The model is even easier to apply than the well-known OECD and Vollenweider models due to more easily accessed driving variables.

The European Union has introduced a new bathing water directive where future classification of recreational waters will be based on the microbial parameters Escherichia coli, and intestinal enterococci. Introduction of enterococci as a new quality parameter may pose a challenge in some areas because relatively less is known about these organisms compared to E. coli. In the present study, the relative abundance of intestinal enterococci, E. coli, and ten fecal sterol and stanol biomarkers were investigated in water and sediment at two estuarine beach sites affected by fecal pollution. In the bathing water, enterococci were relatively more abundant at low E. coli concentrations. In the sediment, enterococci were generally more abundant than E. coli with surface concentrations between 1.0 × 10² and 4.5 × 10³ CFU cm⁻³. Enterococci populations were relatively similar in water and sediment, and were phenotypically different from that of nearby pollution sources. The putative human specific genetic marker esp in Enterococcus faecium was not detected in water or sediment samples despite occasional inputs of human waste from storm water overflows. Sterol and stanol profiles suggested a direct link between water and sediment pollution profiles on days with wind conditions that facilitated resuspension. Sediment resuspension may occur at wind speeds exceeding 6–8 m s⁻¹, and could contribute significantly to enterococci concentrations in the overlying water. The study emphasized that recontamination of the water column due to wind induced resuspension should be considered when evaluating indicator levels and microbial hazards in estuarine recreational waters.

During the seasons 2003/04, 2004/05 and 2005/06, a study was made of the evolution of runoff as well as soil and available P and K losses in the sediment carried away in a conventional till system--that most used at the present time--and in a no till system with added pruning remains in an olive grove of the picual variety located in Torredonjimeno (Jaén, Spain). A group of microplots for sediment collection in a randomized complete block design was established. The samples were collected in the field after each storm. In the study period, a total of 21 storms were recorded, with a precipitation of 450 mm in 2003/04, 179 mm in 2004/05 and 388 mm in 2005/06. The erosivity of the rainfall was characterized and the cover percentage in the plots throughout the time was determined. The establishment of pruning remains reduced soil loss with respect to conventional tillage (CT) in the 3 years (72%). Likewise, the available P loss greatly declined in the study (46.4%) under conservation agriculture. The reduction in available K loss (72.4%) was much greater than that of available P. The close relationship between both variables and sediment production also stands out. Runoff was the parameter on which the pruning remains had the least influence with only an 11% average reduction.

The paper describes a novel approach to reduce ammonia emissions from Concentrated Animal and Feeding Operations (CAFO) in general, and from poultry houses in particular. The approach is based on installing a dedicated air capturing system on the feeding infrastructure that draws air from close to the litter. Air at these locations has NH₃₍g₎ concentrations an order of magnitude higher than at the vents of the ventilation system. Moreover, while the dedicated waste air drawing system can work continuously, the operation of the ventilation system is intermittent and directed towards maintaining the birds climatically-comfort. The NH₃₍g₎ rich waste air is conveyed to an acidic (0 < pH < ~5) bubble column reactor in which ammonia is converted to [Formula: see text]. The reactor operates in a batch mode, starting at pH 0 (1 N HCl solution) and is switched to a new acidic absorption solution just before NH₃₍g₎ breakthrough occurs, at around pH 5. Experiments with a wide range of NH₃₍g₎ concentrations showed that the absorption efficiency is practically 100% throughout the process as long as the face velocity is below 4 cm/s. The advantages of the method include high absorption efficiency, lower NH₃₍g₎ concentrations in the vicinity of the birds, generation of a valuable product (a high concentration ammonia solution) and the separation between the ventilation and ammonia treatment systems. A small scale pilot operation conducted for 5 weeks in a broiler house showed the approach to be technically feasible. A larger scale pilot study is required for fine-tuned cost estimation.

Regulators need a reliable, precise and easy to use tool for predicting the occurrence of pesticides in drain water and catchments in agricultural areas. Occurrence depends on a wide range of substance and site specific factors and this study presents a simple model built on the results from simulations of a detailed model system that does not neglect or omit any of these factors. A drainage dominated sub-catchment (0.03 km²) of the Lillebaek catchment (4.4 km²) on Funen, Denmark, represented by the catchment model MIKE SHE is considered. Detailed analyses have been made with respect to geological and hydrodynamic conditions as well as measurements of pesticide concentrations in ground and surface waters. Maximum concentrations in drain water, the time for reaching this concentration and the time interval for exceeding the limit value have been derived empirically from MIKE SHE simulations using degradation rates and sorption coefficients values for 37 pesticides included in the Danish PATE database. The relatively hydrophilic bentazon and hydrophobic pendimethalin are used as model pesticides for illustration. A simple tool applicable for a wide range of pesticides has thus been designed based on detailed analyses of a limited number of pesticides. The user requirements are degradation rates, sorption coefficients, application rates and regulatory limit values for the pesticides of interest.

Interdisciplinary studies on aquatic environments and cross-validation of laboratory vs. field results will likely increase the need for simultaneous use of large- and small-scale ultrafiltration systems. In this study, a comparison of two ultrafiltration systems differing in scale (PrepScale and PelliconXL, Millipore; membrane areas 0.54 m² and 0.005 m², respectively), was made for the cut-offs 3 and 300 kDa. Large systems are useful for their high permeate throughput, while small systems are necessary when the amount of sample is limited. The ability of PrepScale and PelliconXL systems to provide comparable results for organic carbon fractionation was studied for polysaccharide solutions and natural freshwaters. In the latter, the colloidal proportions of different trace metals (V, Cr, Mn, Co, Ni, Cu, Sb, and U) were also determined. Although the colloidal proportions obtained with PelliconXL 3 kDa were sometimes slightly higher than with PrepScale 3 kDa (principally for DOC and U in natural waters), Mann-Whitney statistical test showed no significant difference in the overall fractionation properties of the two systems. Our observations show that reaching high concentration factors lead to a strong modification of colloids size distribution in the range 50-2,000 nm and thus low concentration factors are preferable to preserve the colloid integrity.

Plant toxicity and chemical removal tests were conducted to investigate the remediation ability of grasses with respect to volatile organic contaminants (VOCs) in contaminated soil and air. Eastern gamagrass (Tripsacum dactyloides) and annual ryegrass (Lolium rigidum) were exposed to artificially contaminated soil or air containing a mixture of 1,1,1-trichloroethane (TCA), trichloroethylene (TCE), and tetrachloroethylene (PCE) under controlled laboratory conditions. The results showed that the grasses are more severely affected in hydroponics than potted soil contaminated with a mixture of these contaminants. It was observed from the results that more contaminants were detected in the shoot and root of plants grown in a closed system with contaminated air than in an open system with contaminated soil. It is suggested from the results that grasses can be used for purification of VOCs from contaminated air especially in a closed system, but the purification effects are likely to be low. The results also suggested that the concentration level of VOCs in shoot, root, and soil could be used as contamination indicator at contaminated sites.

In the present study, during a period of 16 months Colilert 3000 was validated in laboratory and field tests and compared to standard laboratory methods for monitoring of coliforms and E. coli. No false positive/negative results for coliforms/E. coli were found in 80 potable well water samples monitored with the Colilert 3000 and compared to standard methods. Although usage of Colilert 3000 to monitor raw water is not recommended by the manufacturer, the E. coli results of 100 samples were 100% positive by membrane filtration, Colilert 18 and MPN and only 80% positive by the Colilert 3000. In addition, in all positive samples, Colilert 3000 and Colilert 18 showed higher results of two to three orders of magnitude compared to MF and MPN. This significant difference was probably due to the presence of Aeromonas spp. and Vibrio spp. (natural inhabitants of the raw surface water) known to interfere with the Colilert test. Treated surface water was monitored by Colilert 3000 for the presence of coliforms and E. coli. Among the 100 samples tested in parallel by membrane filtration all were negative, while with Colilert 3000 only 76% were negative. Post-test identification of the positive samples did not reveal the presence of E. coli but interfering microorganisms. The last application was to evaluate Colilert 3000 to monitor accidental or deliberate pollution of drinking water with sewage sources. Among 20 samples spiked with raw sewage (0.1 and 1%) all results were positive for both coliforms and E. coli. The time span required for Colilert 3000 to detect positive samples was 6-10 h compared to 24 h with the standard membrane filtration.

The relationships between heavy metal concentrations and physico-chemical properties of natural lake waters and also with chemical fractions of these metals in lake sediments were investigated in seven natural lakes of Kumaun region of Uttarakhand Province of India during 2003-2004 and 2004-2005. The concentrations of Cr, Mn, Fe, Ni, Cu, Zn, Cd and Pb in waters of different lakes ranged from 0.29-2.39, 10.3-38.3, 431-1407, 1.0-6.6, 5.3-12.1, 12.6-166.3, 0.7-2.7 and 3.9-27.1 μg l-¹ and in sediments 14.3-21.5, 90.1-197.5, 5,265-6,428, 17.7-45.9, 13.4-32.0, 40.0-149.2, 11.1-14.6 and 88.9-167.4 μg g-¹, respectively. The concentrations of all metals except Fe in waters were found well below the notified toxic limits. The concentrations of Cr, Mn, Ni, Cu, Zn, Cd and Pb were positively correlated with pH, electrical conductivity, biological oxygen demand, chemical oxygen demand and alkalinity of waters, but negatively correlated with dissolved oxygen. The concentrations of Cr, Ni, Zn, Cd and Pb in waters were positively correlated with water soluble + exchangeable fraction of these metals in lake sediments. The concentrations of Zn, Cd and Pb in waters were positively correlated with carbonate bound fraction of these metals in lake sediments. Except for Ni, Zn and Cd, the concentrations of rest of the heavy metals in waters were positively correlated with organically bound fraction of these metals in lake sediments. The concentrations of Cr, Mn, Ni, Cu and Zn in waters were positively correlated with reducible fraction of these metals in lake sediments. Except for Cd, the concentrations of rest of the metals in waters were positively correlated with residual fraction and total content of these heavy metals in lake sediments.

The mass, ionic and elemental size distributions of particulate matter (PM) measured indoors and outdoors in an apartment situated in a north-westward suburb of Prague are presented. The PM samples were collected by two Berner type low pressure impactors separating particles into 10 size fractions from 26 nm to 10 μm and were further analyzed by ion chromatography (IC) and proton induced X-ray emission (PIXE). Temperature, pressure and relative humidity were measured both indoors and outdoors parallel to PM sampling. The indoor and outdoor PM dynamics were recorded by two scanning mobility particle sizers (SMPS) and an aerodynamic particle sizer (APS). Finally, the ventilation rate was determined by a radon technique. Ion chromatography showed that the major inorganic components of the fine particle mode are sulfate, nitrate, and ammonium with very low indoor nitrate concentration. Crustal elements (Al, Si, Ca, Ti, Mn, and Fe) were associated with the coarse aerosol mode. The presence of people increased the mass concentration of coarse particles, whereas cooking, smoking, and burning of incense and candles contributed predominantly to the fine particle mode. Smoking and the burning of incense also increased the concentration of potassium, bromine and chlorine content in fine particles.