We investigated the coupling of abundance of bacteria, phytoplankton and ciliates with hydrocarbons in the surface water and sediments of five interconnected ponds in the arid Sfax solar salterns. This study aimed at determining the potential sources of hydrocarbons and the effects of salinity gradients on microorganism metabolism. Hydrocarbon analysis was performed by gas chromatography (GC-FID) and gas chromatography coupled with mass spectrometry (GC-MS). The GC-FID allowed the detection of aliphatic hydrocarbons and n-alkanes ranging from n-C₁₃ to n-C₃₀. Total aliphatic hydrocarbon concentrations varied from 92.5 mg. l-¹ in the first pond (having marine characteristics) to 661.1 mg. l-¹ in the last pond (crystallizer) (316.8 ± 120.1 mg. l-¹) for water samples and from 26.7 to 127.8 μg. g-¹ dry weight for sediment samples. The GC-MS enabled us to detect halogenated hydrocarbons (bromoalkanes and chloroalkanes) and n-alkenes. The distribution of n-alkanes indices coupled to several environmental factors suggests that a major fraction of hydrocarbons resulted from both prokaryotic (bacteria) and eukaryotic (protists) developments. A low hydrocarbon fraction might be petrogenic.

Understanding and controlling air pollution in highly populated areas is very important, although interpreting the levels of gaseous pollutants and airborne particulate matter is complicated by dominant natural and anthropogenic emissions, micro-meteorological processes, and chemical reactions which take place directly in the atmosphere. For this reason, it is very difficult to relate the characteristics of air pollution to one or more specific emission sources. The aim of this paper is to detect associations among elements and organic compounds emitted from specific sources by means of chemical analyses, statistical processing of data, seasonal evolution study, and geochemical considerations to trace their origin. A detailed characterization of air quality during the period September 2000-September 2001 was carried out in three locations of the Venice region: A heavy traffic urban site, a public park, and the island centre of the city of Venice. Twenty-eight inorganic elements, four polycyclic aromatic hydrocarbons, CO and benzene were quantified and processed by a statistical procedure based on factor analysis considering variations on a seasonal basis. Results show the presence of associations between elements and compounds with the same behaviour in all sampling points. This indicates that several pollutants originate from a common source, and are then “diluted” throughout the study area, maintaining the imprint of their origin. Pt, polycyclic aromatic hydrocarbons, CO and benzene originating from the exhaust gas of vehicles are all linked in the traffic factor, whereas Cd is associated with Se, having a common source in industrial processes.

A conceptual model of solute transport with bioremediation processes using sawdust as a matrix to improve the efficiency of bioremediation in porous media is presented. The transport part of the model solves the advection dispersion differential equations and the reaction part describes the heterotrophic metabolisms of several groups of bacteria. The bacterial growth is formulated using the double Monod kinetic equation. The model depicts the utilization of oxygen, nitrate, manganese, iron oxides and sulfate as electron acceptors for oxidation of organic carbon in porous media. Exchange between the different phases (mobile pore water phase, bio phase and matrix phase) is also considered in this model. Model parameters were adopted from literature on bioremediation processes. Feasibility and applicability of parameters were assessed by conducting a laboratory soil-sawdust columns experiments and comparing the simulated results with the experimental data. The results indicate that sawdust could be employed as low-cost materials to enhance the bioremediation processes in porous media. While the availability of organic carbon is one of the most important factors that affect bacterial activity in porous media, this study demonstrates that using sawdust as a carbon source can improve the bacterial activity and increase the column permeability.

Lake St. Pierre (LSP), constituted of a 120 km² stretching of the St. Lawrence River (Southern Québec), hosts the largest freshwater fishery industry in Canada. The lake drains, through its main tributaries, an important area of agrarian land and was subjected to intense industrial activities in the past century. In this paper, we present (1) an estimation of the seasonal aquatic mercury (Hg) inputs to LSP from the St-Lawrence River and two major tributaries; (2) a reconstruction, by the analysis of sediment cores, of the historic inputs of Hg into LSP and in a large riparian wetland, Bay St. François. Our results indicate that the aquatic Hg inputs to LSP (290 kg Hg between April 2003 and April 2004) are moderately elevated with most of the inputs occurring from the St. Lawrence River, either in spring or early winter, during high flow episodes. The sediment profiles suggest a recent decrease in Hg inputs, likely attributable to improvements of industrial practices. The observed perturbation of the surface sediments give evidence of an active hydrodynamic regime, suggesting that LSP could only act as a transitory system for suspended sediment and Hg, with seasonal accumulation and recurrent re-suspension resulting from changes in the hydrodynamic regime. Finally, we observed positive MeHg fluxes from the sediment to the water at different seasons in Bay St. François. However, Hg levels in fish like walleyes of LSP are reported to be low, which could be explained by faster fish growth rates following in part intense fishing pressure in LSP.

The immobilization of lead by the reaction with phosphate bearing materials is a promising remediation method for contaminated soils. Low soluble neo-formed lead-phosphate phases similar to chloropyromorphite [Pb₅(PO₄)₃Cl], can control availability and mobility of lead in the environment, and consequently reduce human exposure, if soils are the main contamination pathway. We used three phosphate source materials [NaH₂(PO₄)₃, commercial superphosphate and phosphate rock] to study lead immobilization in soil and mining waste samples. Products were examined after 1, 3 and 6 months of contact. The samples are from a contaminated area by former Pb mining and smelting activities, in southeastern Brazil, where epidemiological studies showed high lead blood levels in local population. The PBET (physiological based extraction test) bioaccessibility test was used to measure changes in the amount of soluble lead after sample treatment. Results show that the most efficient phosphate source was NaH₂(PO₄)₃, which reduced lead solubility to 92% in acidic gastric conditions after the first month of contact. Superphosphate and phosphate rock also diminished Pb solubility, but the effect was more time dependent. None specific Pb-phosphate phases could be identified by XRD in whole treated samples, but the Pb-Ca-P elemental associations, observed on SEM images and EDS spectra of portions of the samples, combined with the reduced solubility, indicate that more insoluble lead phases were formed after the treatment. Based in these results, the in site phosphate application on soils to induce lead immobilization should be considered as a possible alternative to reduce human exposure at the area.

Spectroscopic (XRD, XPS, ICP-MS and AAS) and microscopic (ESEM) techniques have been used in order to study the chemical effects with emphasis on mercury speciation, during thermal treatment of a mercury contaminated soil. In the untreated soil, mercury was found concentrated in spherical particles, which were successively broken down upon thermal treatment. Hg⁰ and inorganic mercury compounds (presumably HgO(s) and HgSO₄(s)) could be detected. No (CH₃)₂Hg and only traces of CH₃Hg⁺ could be found. The dependence on temperature and heating time indicated that the evaporation of mercury from the soil was partly controlled by diffusion mechanisms. Mercury volatilized in two separate stages during heating; initial elemental vaporization, and subsequent volatilization of the oxide or sulfate phase at higher temperatures (>230°C). By thermal treatment at 470°C and 20 min, a removal of >99% of the mercury could be achieved.

A critical load data base was developed for Europe and Northern Asia using the latest data bases on soils, vegetation, climate and forest growth. Critical loads for acidity and nutrient nitrogen for terrestrial ecosystems were computed with the Simple Mass Balance model. The resulting critical loads are in accordance with critical loads from previous global empirical studies, but have a much higher spatial resolution. Critical loads of acidity are sensitive to both the chemical criterion and the critical limit chosen. Therefore a sensitivity analysis of critical loads was performed by employing different chemical criteria. A critical limit based on an acid neutralizing capacity (ANC) of zero resulted in critical loads that protect ecosystems against toxic concentrations of aluminium and unfavourable Al/Bc ratios, suggesting that ANC could be an alternative to the commonly used Al/Bc ratio. Critical loads of nutrient nitrogen are sensitive to the specified critical nitrate concentration, especially in areas with a high precipitation surplus. If limits of 3-6 mg N l⁻¹ are used for Western Europe instead of the widely used 0.2 mg N l⁻¹, critical loads double on average. In low precipitation areas, the increase is less than 50%. The strong dependence on precipitation surplus is a consequence of the simple modelling approach. Future models should explore other nitrogen parameters (such as nitrogen availability) instead of leaching as the factor influencing vegetation changes in terrestrial ecosystems.

Steamboat Creek, Washoe County, Nevada, is considered the most polluted tributary of the Truckee River, therefore the reduction of nutrients from the creek is an important factor in reducing eutrophication in the lower Truckee River. Restoration of the wetlands along the creek has been proposed as one method to improve water quality by reducing nutrient and sediments from non-point sources. This study was aimed to design a simulation model wetlands water quality model (WWQM) that evaluates nitrogen, phosphorus, and sediments retention from a constructed wetland system. WWQM is divided into four submodels: hydrological, nitrogen, phosphorus, and sediment. WWQM is virtual Visual Basic 6.0 program that calculates hydrologic parameters, nutrients, and sediments based on available data, simple assumptions, knowledge of the wetland system, and literature data. WWQM calibration and performance was evaluated using data sets obtained from the pilot-scale constructed wetland over a period of four and half years. The pilot-scale wetland was constructed to quantify the ability of the proposed wetland system for nutrient and sediment removal. WWQM simulates nutrient and sediments retention reasonably well and agrees with the observed values from the pilot-scale wetland system. The model predicts that wetlands along the creek will remove nitrogen, phosphorus, and sediments by 62, 38, and 84 %, respectively, which would help to reduce eutrophication in the lower Truckee River.

In this paper a three-step procedure is proposed to deal with ecological data, usually very complex in their treatment. The three steps – exploratory, confirmatory, and modelling phases – reflect the different methodological approaches necessary in each phase of the study. To illustrate the methodology, a case study is proposed, concerning the suitability of plants as pollution bioindicators. Samples of differently aged Pinus pinea L. needles were collected throughout 1 year in three different locations, whose human disturbance was known to be different. In the samples some morphological and functional parameters were measured, whose relation with the stress was already known. The exploratory analysis suggested pollution with human origin, the needle’s age, and the environmental conditions as the main factors of influence of damage. The confirmatory analysis confirmed both site and age as main factors and occasionally the sampling date. On this basis, some models were estimated separately for each site: models that best described the damage as function of age resulted non-linear and some of them with seasonal fluctuations. As a result, whereas the models described well enough the pollution temporal variation, the difference of pollution in the sites was best described by the different values of the models parameters in the different sites. In short, different pollution conditions are described better by the damage trend than by the individual measures. The three-step procedure resulted of high utility in outlining the most interesting relations to investigate through the modelling, the opportunity to model the indicators variation along time separately for each site, and to introduce the seasonal variation in some models.

The selectivity and uptake capacity of horticultural peat available in Romania was evaluated with respect to the removal of Cd(II), Cr(VI) and Pb(II) ions from aqueous solution. The kinetics, sorption capacities, selectivity and pH dependence of sorption were determined. The influence of metal concentration in solution is discussed in the terms of Langmuir and Freundlich isotherm and constants. Sorption capacities increased with increasing metal concentration in solution. For solutions containing 300 mg/l of metal, the observed uptake capacities were 20 mg Cd(II)/g peat, 15 mg Cr(VI)/g peat and 30 mg Pb(II)/g peat. The study proved that horticultural peat is a suitable material for the removal of the studied heavy metal ions from aqueous solutions, achieving removal efficiencies higher than 90%, and could be considered as a potential material for treating effluent polluted with Cd(II), Cr(VI) and Pb(II) ions.