Although the attention for vanadium (V) as a potentially harmful element is growing and some countries adopted threshold values for V in soils, sediments, groundwater, or surface water, V is generally of little importance in environmental legislation and the knowledge about the behavior of V in the environment is still limited. In the present study, the release of V from oxidized sediments, sediment-derived soils, and certified reference materials was investigated by means of several types of leaching tests and extractions that are frequently used for soil and sediment characterization. The pHₛₜₐₜleaching tests and single and sequential extractions applied in this study show that V generally displays a very limited actual and potential mobility in sediment. “Mobile” V concentrations, as estimated by the amount of V released by a single extraction with CaCl₂0.01 mol L⁻¹, were low, even in the most contaminated sediment samples. Only under strongly acidifying conditions (pH 2), such as in the case of ingestion of soil or sediment or in accidental spills, a substantial release of V can be expected.

In the present study, the photolysis of carbofuran has been undertaken under sunlight conditions and at the surface of model supports such as clay films and different soils collected from two different sites in Morocco (Tirs and Dahs). In all conditions, an efficient degradation occurred owing to direct light absorption and also to photoinduced processes involving either clays or natural organic matter moities. On kaolin films, the photodegradation kinetics appears to follow a first-order process that clearly depends on the film thickness. The diffusion of carbofuran from the lower part to the illuminated surface was found to be negligible when compared to the photolysis process within the range of 20–70 μm. Thus, the photolysis rate constant at the surface of the solid support, k⁰, was evaluated to be 7.0 × 10⁻³ min⁻¹. Under these experimental conditions, the quantum yield was found equal to 2.1 × 10⁻⁴. On soil surfaces, the disappearance rate constant was mainly attributed to photoinduced processes arising from natural organic matter. From the analytical point of view, the products were formed through (1) hydroxylation on the aromatic ring, (2) homolytic scission of the carbamate C–O bond leading to radical species formation, and (3) photohydrolysis of the carbamate C–O bond.

The aim of our studies was to determine the efficiency of decomposition of non-ionic surfactant by the Fenton method in the presence of iron nanocompounds and to compare it with the classical Fenton method. The subject of studies was water solutions of non-ionic detergent Tergitol TMN-10 used in textile industry. Water solutions of the surfactant were subjected to treatment by the classical Fenton method and to treatment in the presence of iron nanocompounds. In the samples of liquid solutions containing the surfactant, chemical oxygen demand (COD) and total organic carbon (TOC) were determined. The Fenton process was optimized based on studies of the effect of compounds used in the treatment, doses of iron and nanoiron, hydrogen peroxide and pH of the solution on surfactant decomposition. Iron oxide nanopowder catalyzed the process of detergent decomposition, increasing its efficiency and the degree of mineralization. It was found that the efficiency of the surfactant decomposition in the process with the use of iron nanocompounds was by 10 to 30 % higher than that in the classical method. The amounts of formed deposits were also several times smaller.

An indoor/outdoor monitoring programme of PM₁₀ was carried out in two sports venues (a fronton and a gymnasium). Levels always below 50 μg m⁻³ were obtained in the fronton and outdoor air. Due to the climbing chalk and the constant process of resuspension, concentrations above 150 μg m⁻³ were registered in the gymnasium. The chalk dust contributed to CO₃ ²⁻ concentrations of 32 ± 9.4 μg m⁻³ in this sports facility, which represented, on average, 18 % of the PM₁₀ mass. Here, the carbonate levels were 128 times higher than those registered outdoors. Much lower concentrations, around 1 μg m⁻³, were measured in the fronton. The chalk dust is also responsible for the high Mg²⁺ concentrations in the gym (4.7 ± 0.89 μg m⁻³), unfolding a PM₁₀ mass fraction of 2.7 %. Total carbon accounted for almost 30 % of PM₁₀ in both indoor spaces. Aerosol size distributions were bimodal and revealed a clear dependence on physical activities and characteristics of the sports facilities. The use of climbing chalk in the gymnasium contributed significantly to the coarse mode. The average geometric mean diameter, geometric standard deviation and total number of coarse particles were 0.77 μm, 2.79 cm⁻³ and 28 cm⁻³, respectively.

The horizontal and vertical distribution patterns and contamination status of ten trace metal/metalloids (Ag, Bi, Co, Cr, Ge, In, Ni, Sb, Sn, Tl) in soils around one of the largest Chinese Pb–Zn smelter in Zhuzhou City, Central China, were revealed. Different soil samples were collected from 11 areas, including ten agricultural areas and one city park area, with a total of 83 surface soil samples and six soil cores obtained. Trace metal/metalloids were determined by inductively coupled plasma–mass spectrometry after digestion by an acid mixture of HF and HNO₃. The results showed that Ag, Bi, In, Sb, Sn, and Tl contents decreased both with the distance to the Pb–Zn smelter as well as the soil depth, hinting that these elements were mainly originated from the Pb–Zn smelting operations and were introduced into soils through atmospheric deposition. Soil Ge was influenced by the smelter at a less extent, while the distributions of Co, Cr, and Ni were roughly even among most sampling sites and soil depths, suggesting that they were primarily derived from natural sources. The contamination status, as revealed by the geo-accumulation index (Igₑₒ), indicated that In and Ag were the most enriched elements, followed by Sb, Bi, and Sn. In general, Cr, Tl, Co, Ni, and Ge were of an uncontaminated status.

Perchlorate concentrations in rice samples from many different provinces, and correlation with surface water contamination, were investigated in the Republic of Korea. Perchlorate levels in the 51 rice samples purchased from local markets ranged from below the detection limit to 1.79 ± 0.39 μg/kg with a mean level of 0.21 μg/kg and 7 samples collected from the Nakdong River watershed ranged from 0.38 ± 0.1 to 3.23 ± 0.47 μg/kg with a mean level of 0.9 μg/kg. The correlation coefficient between perchlorate levels in rice samples from the Nakdong river watershed and the levels in surface water was estimated to be approximately 0.904 in the 95 % confidence interval. These results show that surface water contamination was highly related to the perchlorate pollution of rice in the Republic of Korea.

In this study, impact of dispersed oil on cardiac mitochondrial function was assessed in a key species of Arctic marine ecosystem, the polar cod Boreogadus saida. Mature polar cod were exposed during 48 h to dispersed oil (mechanically and chemically) and dispersants alone. The increase observed in ethoxyresorufin-O-deethylase activity and polycyclic aromatic hydrocarbon metabolites in bile indicated no difference in contamination level between fish exposed to chemical or mechanical dispersion of oil. Oil induced alterations of O₂consumption of permeabilised cardiac fibres showing inhibitions of complexes I and IV of the respiratory chain. Oil did not induce any modification of mitochondrial proton leak. Dispersants did not induce alteration of mitochondrial activity and did not increase oil toxicity. These data suggest that oil exposure may limit the fitness of polar cod and consequently could lead to major disruption in the energy flow of polar ecosystem.

The use of pesticides to increase agricultural production can result in the contamination of the environment, causing changes in the genetic structure of organisms and in the loss of biodiversity. This practice is also inducing changes in the rainforest ecosystem. In this work, a Pseudomonas aeruginosa isolated from a preservation soil area of the Brazilian Amazon Forest, without usage of any pesticide, was evaluated for its potential to degrade atrazine. This isolate presented all responsible genes (atzA, atzB, atzC, atzD, atzE, and atzF) for atrazine mineralization and demonstrated capacity to use atrazine as a nitrogen source, having achieved a reduction of 44 % of the initial concentration of atrazine after 24 h. These results confirm gene dispersion and/or a possible contamination of the area with the herbicide, which reinforces global concern of the increase and intensive use of pesticides worldwide.

In recent years, the application of titanium dioxide (TiO₂) as a photocatalyst in asphalt pavement has received considerable attention for purifying ambient air from traffic-emitted pollutants via photocatalytic processes. In order to control the increasing deterioration of ambient air quality, urgent and proper risk assessment tools are deemed necessary. However, in practice, monitoring all process parameters for various operating conditions is difficult due to the complex and non-linear nature of air pollution-based problems. Therefore, the development of models to predict air pollutant concentrations is very useful because it can provide early warnings to the population and also reduce the number of measuring sites. This study used artificial neural network (ANN) and neuro-fuzzy (NF) models to predict NOₓconcentration in the air as a function of traffic count (Tᵣ) and climatic conditions including humidity (H), temperature (T), solar radiation (S), and wind speed (W) before and after the application of TiO₂on the pavement surface. These models are useful for modeling because of their ability to be trained using historical data and because of their capability for modeling highly non-linear relationships. To build these models, data were collected from a field study where an aqueous nano TiO₂solution was sprayed on a 0.2-mile of asphalt pavement in Baton Rouge, LA. Results of this study showed that the NF model provided a better fitting to NOₓmeasurements than the ANN model in the training, validation, and test steps. Results of a parametric study indicated that traffic level, relative humidity, and solar radiation had the most influence on photocatalytic efficiency.

XAD-2 resin-based passive samplers (PAS) with dimensions adapted to 100 mL accelerated solvent extraction cells were used to study the temporal and spatial variations of 17 PAHs on five sites in the atmosphere of southern Luxembourg. This new design allowed extracting the PAS without emptying the resin from the shelter. PAH analyses were done with gas chromatography–tandem mass spectrometry. PAS were deployed for 1 year with varying sampling periodicities, and 16 PAHs were detected with concentrations ranging from 1 ng/PAS for chrysene to 9,727 ng/PAS for naphthalene. The PAS were found adapted to the monitoring of temporal and spatial variations for lightweight PAHs (up to four aromatic rings) though not for heavy PAHs with five aromatic rings or more, as these compounds are preferably in the particle phase of the atmosphere and the amount of these PAHs trapped on the PAS will be too low.