We investigated concentrations of dissolved organic carbon (DOC) in throughfall and soil solutions at 5, 15 and 40-cm depth in 16 Norway spruce and two Scots pine plots throughout Norway between 1996 and 2006. Average DOC concentrations ranged from 2.3 to 23.1 mg/l and from 1.1 to 53.5 mg/l in throughfall water and soil solutions, respectively. Concentrations of DOC in throughfall and soil waters varied seasonally at most plots with peaks in the growing season. By contrast to recently reported positive long-term trends in DOC concentrations in surface waters between 1986 and 2003, soil water data from 1996 to 2006 showed largely negative trends in DOC concentrations and no significant trends in throughfall. However, regression analysis for individual sites, particularly at 5- and 15-cm soil depths, showed that DOC concentrations in soil water were significantly and negatively related to non-marine sulphate (SO₄) and chloride (Cl⁻). The lack of a long-term increase in DOC in soil water in the period May 1996-December 2006 may be due to the relatively small changes in the deposition of SO₄ and Cl⁻ in this period.

Assessing air quality in street canyons is a crucial concern, as the highest pollution levels and threshold exceedances are usually experienced within this kind of urban streets. A brief overview based on experimental studies and modelling techniques undertaken in literature is presented, including characteristic features affecting wind flow and pollutant dispersion within street canyons. In this work, a numerical street canyon model intercomparison has been performed in a typical urban canyon in Florence, Italy. In particular, STREET, Canyon Plume Box Model (CPBM) and Operational Street Pollution Model (OSPM) have been applied to compute the street-level 1-h carbon monoxide (CO) concentrations. In addition, the CALINE4 model has been applied to test the site morphology. Input data cover a 1-year time period and include meteorological observations as well as measured traffic volumes and driving speeds. Hourly road emissions have been calculated using the COPERT methodology taking into account vehicle fleet, traffic flows and driving speed, as well as ambient temperature to account for cold overemissions. A preliminary experimental data analysis has been carried out in order to investigate the dependence of observed CO concentrations on meteorological and traffic parameters. Hourly CO concentrations observed over the full year have been used to compare the STREET, CPB and OSP models, resulting in a detailed statistical analysis carried out by wind sector as well as on a seasonal basis.

Highway detention ponds can fill with sediments from runoff water loaded with traffic-related materials. Sediment disposal is problematic and various protocols are currently studied, including phytoremediation. Here we present a preliminary study on four highway detention ponds in southern France to identify key sediment characteristics. Our objectives were to characterize metal content and physicochemical properties of the sediments and to evaluate the role of charophytes, which grow spontaneously in ponds, on metal lability. Vegetated and non-vegetated areas were compared. The lability of Mn, Cu, Zn, and Pb complexes was greater in the presence of charophytes. No variation in grain size composition was observed between non-vegetated and vegetated areas. These results may be useful to implement a phytoremediation strategy using those spontaneous charophytes. Our results suggest that local factors may impact sediment characteristics: for instance, strong gusts of wind, typical of southern France climate, may blow particles (some of them not related to traffic) in and out of detention ponds.

Rates of biosorption of cadmium and copper ions by nonliving biomass of the brown macroalga Sargassum sinicola under saline conditions were studied. Batch experiments show that the ability to remove cadmium is significantly diminished (from 81.8% to 5.8%), while the ability to remove copper remains high (from 89% to 80%) at a range of salinity from 0 to 40 psu. Maximum capacity of biosorption at 35 psu was 3.44 mg g⁻¹ for cadmium and 116 mg g⁻¹ for copper. The presence of salt did not significantly affect the rate of biosorption, which was about 90% of saturation in 60 min for both metals. There is an antagonistic effect on biosorption when both metals are present in the solution.

The impact of autochthonous anaerobic bacteria on the release of metals in river sediment was studied. The sediments were characterized and bacterial activity was monitored in a batch reactor, where the sediments were incubated with a synthetic substrate solution containing glucose as carbon source. The results showed that metal release was correlated to the bacterial growth (carbon mineralization). In particular, a relationship between iron reduction and metal release was observed indicating that iron-reducing bacteria had a strong influence. By reductive dissolution of iron oxides, bacteria also released their associated toxic elements into the liquid phase. While organic analysis showed acetate and butyrate production leading to a decrease in pH and indicating a Clostridium fermentative bacteria activity, the results did not indicate any direct role of organic acids in the dissolution of iron and their associated metals.

This work aimed to determine the sensitivity of acetylcholinesterase (AChE) and glutathione S-transferases (GST) activities of Crangon crangon (L.) to the water-accommodated fraction (WAF) of the fuel oil spilled by the oil tanker Prestige, in order to assess their usefulness as markers for this kind of pollution. Laboratory exposure of shrimps to WAF of weathered Prestige fuel oil showed no significant interference with AChE activity. Significant induction of GST activity was observed, potentially as a result of high concentrations of polycyclic aromatic hydrocarbons. However, these results were only obtained with the higher WAF concentrations tested. It was concluded that AChE and GST activities of C. crangon were not useful biomarkers for short-term exposure to the WAF of fuel oil spilled by the tanker Prestige and carried to the beaches of Galicia (NW Spain).

The fluxes of N-NO ₃ ⁻ , N-NH ₄ ⁺ , S-SO ₄ ²⁻ , Na⁺, K⁺, Ca²⁺ and Mg²⁺ from bulk precipitation to throughfall, stemflow and soil water surface flows were studied during 1999-2003 in planted Norway spruce forest stands of different ages (11, 24, 91 and 116 years in 1999). Also, runoff from the corresponding Potok Dupniański Catchment in the Silesian Beskid Mts was studied. N deposition was above the critical load for coniferous trees. The interception increased with stand age as well as leaf area index and so did the leaching from the canopy of almost all the analysed elements, but especially S-SO ₄ ²⁻ , H⁺ and K⁺. The nutrient fluxes varied with age of the spruce stands. Throughfall showed a high amount of S and of the strong acids (S-SO ₄ ²⁻ and N-NO ₃ ⁻ ) deposited to the soil, especially in older spruce age classes. Decomposition of organic matter caused a rise in water acidity and an increase in the concentrations of all the analysed ions; the leaching of minerals, however, was low (under 1%). The horizontal soil water flow showed an increase in the amount of water and amount of ions and contributed to a further decrease of pH at the soil depth of 20 cm. Element concentrations and their amounts increased with water penetrating vertically and horizontally on the slopes. Considerable amounts of ions, especially S and alkaline cations, were carried beyond the reach of the root system and then left the catchment. In the long term, these mineral losses will adversely affect health and growth of the spruce stands, and the increased acidity with stand age will presumably have negative effects on the runoff water ecosystem.

Decolorization of six synthetic dyes and two raw textile effluents (A and B) by eight basidiomycetous fungi was investigated. Among eight basidiomycetous fungi, fungal isolate RCK-1 decolorized textile effluent A maximally (42%), while fungal isolate RCK-3 was found to decolorize more of Congo Red (69%), Xylidine Ponceau 2R (100%), Poly R-478 (96%), Indigo Carmine (99%), Lissamine Green B (90%), Toluidine Blue (57%) and textile effluent B (54%), than the rest of fungi. Percentage decolorization of all synthetic dyes and textile effluents by the new fungal isolates RCK-1 and RCK-3 was higher compared to the most widely studied simultaneous lignin degrader, Phanerochaete chrysosporium and selective lignin degrader, Pycnoporus cinnabarinus, when tested in liquid cultures. A statistically significant positive correlation between laccase production and decolorization of dyes and effluents was obtained as compared to other ligninolytic enzymes (lignin peroxidase and manganese peroxidase) production. This showed the importance of the differential contribution of the different ligninolytic enzymes towards the decolorization of the synthetic dyes and textile effluents. The substantially higher ligninolytic enzyme production by the fungal isolates RCK-1 and RCK-3 also suggested their potential use for textile effluent treatment and other possible biotechnological applications.

The release of heavy metals in aquatic systems due to the discharge of industrial wastewaters is a matter of environmental concern. Heat-inactivated cells of a flocculent strain of Saccharomyces cerevisiae were used in the bioremediation, in a batch mode, of a real electroplating effluent containing Cu, Ni, and Cr. In this approach, no previous reduction of Cr(VI) to Cr(III) was required. Cr(VI) was selectively removed (98%) by yeast biomass at pH 2.3. At this pH, Cr(VI) is mainly in the form of HCrO ₄ ⁻ and yeast surface is surrounded by H⁺ ions, which enhance the Cr(VI) interaction with biomass binding sites by electrostatic forces. Subsequently, pH of the effluent was raised up to 6.0; this pH maximizes the efficiency of cations removal since at this pH the main binding groups of yeast cells are totally or partially deprotonated. The passage of effluent through a series of sequential batches, at pH 6.0, allowed, after the third batch, the removal of Cu(II), Ni (II), Cr total, and Cr(VI) in the effluent to values below the legal limit of discharge. The strategy proposed in the present work can be used in plants for the treatment of heavy metals rich industrial effluents containing simultaneously Cr(VI) and Cr(III).