Over 5 days, Brassica juncea removed 54% of the highly toxic insecticide phorate from the medium with the formation of phorate sulfoxide in small quantity. The loss of phorate from the medium followed first-order kinetics. The half-life of phorate disappearance from water decreased by ~4.5-fold in the presence of B. juncea. Mild phorate phytotoxicity was evident from the elevated activities of the antioxidative enzymes like glutathione-disulfide reductase, glutathione S-transferase, superoxide dismutase, and catalase in the plants. Nevertheless, the ubiquitous antioxidative peroxidase was not significantly increased, nor the total glutathione content, due to phorate exposure. Phosphotriester bond hydrolysis and glutathione S-transferase-mediated conjugation seemed to be the key reactions for phorate metabolism by B. juncea. From the limited information available, for the first time, a tentative mapping of phytotransformation pathways was performed.

The main objective of this study was to examine the effect of an electro-Fenton pretreatment on the biodegradability of sulfamethazine-polluted solutions. The aim of the pretreatment was only to degrade this molecule in order to increase the biodegradability of the effluent and therefore allow a subsequent biological treatment. Preliminary tests showed the absence of biodegradability of the target compound. The degradation of sulfamethazine by electro-Fenton process was then examined using a carbon felt cathode and a platinum anode in an electrochemical reactor containing 1 L of solution. The influence of some experimental parameters such as initial concentration, temperature and current intensity on the degradation by electro-Fenton step has been investigated. In addition, the biodegradability of the solution after electrochemical pretreatment was examined and showed a Biological Oxygen Demand (BOD5) on Chemical Oxygen Demand (COD) ratio above the limit of biodegradability, namely 0.4, for several experimental conditions. The feasibility of coupling an electro-Fenton pretreatment with a biological degradation of by-products in order to mineralize polluted solutions of sulfamethazine was confirmed.

Sodium chloride is the most often used chemical to malt ice and snow on the roads and has negative effects on the roadside environment. Searching for ways to improve the conditions for growth of trees and shrubs near the roads becomes an urgent matter. One such method of improving growth conditions for plants under salinity might be to use organic matter (green waste compost) and mycorrhizal fungi. This study studied the effect of application in soil different salts on several trees and shrubs growth in growing media. Also, effect of green waste compost and arbuscular mycorrhiza (AM) added to the growing medium was evaluated in terms of growth and K+, Ca+2, and Na+ uptake. The highest pH of the growing medium was noted when sodium carbonate was used. The pH ranged from 8.7 to 9.0 after eight doses of sodium carbonate. The pH of the growing medium was also significantly higher regardless of whether or not green waste compost or mycorrhizal fungi were used. The type of growing medium had a great effect on the growth of most of the trees, but among shrubs the growing medium was only important for Cornus alba, Sambucus nigra, and Spiraea vanhouttei. Growth of all these plants was much better under salinity when green waste compost or green waste compost with AM fungi was used. In all the cases, when salinity of the growing medium retarded growth of trees and shrubs, sodium chloride was the compound that had the strongest growth retarding effect. Leaf ionic composition was significantly affected by salinity in the growing medium, and in some cases also by micorhizal fungi. The type of growing medium had various effects on sodium uptake, depending on species. In most cases, the addition of green waste compost to the growing medium caused a greater amount of sodium in the leaves of tested plants. The use of mycorrhizal fungi had no effect on the uptake of sodium, compared to the control plants (without AM fungi).

The high hydrophobicity of polycyclic aromatic hydrocarbons (PAHs) is the main limiting factor for the remediation of soils and aquifers. Surfactants are amphiphilic substances which encourage the transfer of hydrophobic compounds from the solid to the liquid phase. While the interaction between organic matter and surfactants has been widely studied, there is a lack of knowledge concerning the relationship between surfactant efficiency and the granulometry of soil and/or geologic material. In this paper, three non-ionic surfactants (Tween 80, Gold Crew, and BS-400) were used to study the desorption of pyrene, chosen as a representative PAH, in soils with different grain size proportions (1%, 5%, 10%, and 20% of clay and silt) and no organic matter (<0.1%). The best quantity of surfactant to apply is closely related to the proportion of fine materials. Tween 80 gave better maximum desorption than Gold Crew and BS-400 (89%, 40%, and 36%, respectively). As an important proportion of aquifers show fine material above 1%, the effective critical micellar concentration obtained when applying surfactants to this type of geologic materials has to be higher than 150 mg L−1 for Tween 80, and higher than 65 mg L−1, and 100 mg L−1 for Golf Crew and BS 400, respectively. Furthermore, results indicate that carrying out simple laboratory tests before the use of surfactants on a field scale is necessary to improve the efficiency and minimize the financial and environmental impact of its application.

Currently, there are five known types of mercury transporters in bacteria: MerC, MerE, MerF, MerH, and MerT. Their general function is to mediate mercuric ion uptake into the cell in preparation for reduction to Hg°. They are present in several bacterial phyla and comprise five distinct families. We have utilized standard statistical bioinformatic tools and the superfamily principle to show that they are related by common descent. After using programs such as Global Alignment Program and SSearch to establish homology, we aligned and analyzed their amino acid sequences to find a single well conserved motif. Although these proteins exhibit 2, 3, or 4 transmembrane helical segments (TMSs), TMSs 1 and 2 are common to all superfamily members. An ancestral sequence was determined, and reliable phylogenetic trees were constructed. The results support the conclusion of homology, establishing that these proteins belong to a single superfamily. This important discovery allows extrapolation of information about structure, function, and mechanism from one protein to all superfamily members to degrees inversely proportional to their phylogenetic distances.

A new sampling system has been developed for the measurement of time-averaged concentrations (TWA) and diffusion coefficients of organic micropollutants in aquatic environments. The system is based on the diffusion of targeted organic compounds through a rate-limiting membrane and the subsequent accumulation of these species in a bound, hydrophobic solid-phase material. Two separate prototype systems are described. One is suitable for the sampling of carbamates such as carbaryl, carbofuran, 3-hydroxycarbofuran, baygon, propham, clorpropham, and the other one for s-triazines such as atrazine, prometryn, propazine, simazine, terbuthylazine, terbutryn, metribuzin, cyanazine, and metamitron pesticides. The systems use solid-phase material (47-mm C₁₈ Empore disk) as the receiving phase but are fitted with rate-limiting membranes of either polysulfone or polycarbonate. For the two designs investigated, the cumulative uptake of all target analytes was considered over exposure periods of 7 days. The determined sampling rates ranged from 0.1323 to 0.0465 L day⁻¹ with both membranes. The best system was the one with the polysulfone membrane allowing a better cumulative uptake.

Three novel composite adsorbents, sulfate-coated zeolite (SCZ), hydrotalcite (SCH), and activated alumina (SCAA), were characterized and employed for the removal of phosphate from aqueous solution using equilibrium and kinetic batch experiments. Scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray diffraction spectrum were used to study the surface characteristics of the coated layer. Equilibrium tests showed that the adsorption of phosphate followed both Langmuir and Freundlich isotherms. The powder-type SCZ was better for phosphate removal (maximum binding energy, β = 111.49 mg g−1) compared to hydrotalcite and activated alumina. The adsorption of phosphate was considered to take place mainly by ion exchange. The kinetic data followed a pseudo-second-order kinetic model. The initial adsorption of phosphate onto the sulfate-coated adsorbents was fast, indicating that the sulfate-coated materials developed in this study can be used as promising adsorbents for the removal of phosphate from wastewater or sewage.

Recently, specific air quality problems have been detected in the northern region of Portugal. The nitrogen oxide (NO₂) annual limit value has been surpassed at several air quality monitoring stations in the northern region, and according to European legislation, air quality plans must be designed and implemented to reduce those levels. The analysis of the air quality data from the stations concerning NO₂ exceedances indicates that traffic is responsible for an increase of more than 40 % compared with the urban background value. Specific measures to reduce NOx emissions have been selected and are related not only mainly to the traffic sector but also to the industrial and residential combustion sectors. The main objective of this study is to investigate the impact of the selected measures on the ambient levels of NO₂ in northern Portugal using a numerical modelling tool—The Air Pollution Model (TAPM). TAPM was applied over the study region using a 120 × 120-km² simulation domain and a spatial resolution of 4.8 × 4.8 km². The entire year of 2010 was simulated and was set as the base year to analyse the impact of the selected measures. Two scenarios have been defined and simulated: the base situation, which considers current NOx emissions, and the reduction scenario for which NOx emissions were re-estimated considering the implementation of the measures. The modelling results demonstrate a decrease of 4–5 μg m⁻³ in the annual NO₂ levels in the study region. Moreover, the implementation of the selected measures will allow compliance with the NO₂ annual limit values in three of the five air quality stations that measured levels surpassing those established by legislation. This situation demands additional measures that should be implemented at the local level and that particularly focus on the traffic sector.

This study investigates pentachlorophenol (PCP) adsorption by the white-rot fungus Anthracophyllum discolor in a fixed-bed column reactor. PCP adsorption at different concentrations (20, 30, and 50 mg L−1) and pH values (5.0, 5.5, and 6.0) was determined and modeled using the Thomas model. Fourier transform infrared spectroscopy (FTIR) was used to identify functional groups of biomass that may participate in the interaction of PCP. The biosorption capacity of A. discolor was pH-dependent, and the PCP adsorbed increased with the decrease in the pH solution. Acid pH values of the influent gave an increase in saturation time in all PCP concentrations. By contrast, the increase in PCP concentration caused that the binding sites were filled quickly, resulting in a decrease in saturation time. The Thomas model was found suitable for describing the entire dynamic of the column with respect to the PCP concentration and pH of the solution. FTIR results showed that amines, carboxylates, alkanes, and C–O groups might participate in the PCP adsorption on the biomass surface. It was concluded that A. discolor biomass was a good adsorbent for PCP removal from influent with mainly acidic pH.

Microbial processes have shown promise for the remediation of uranium and nitrate in groundwater impacted by uranium mine tailings. This study investigated the inhibitory impact of uranium(VI) towards different microbial populations in anaerobic biofilms, including methanogenic, denitrifying, and uranium-reducing microorganisms, which are commonly found at uranium bioremediation sites. Results of batch activity bioassays indicated a very distinct level of toxicity depending on the targeted microbial community. U(VI) caused severe inhibition of acetoclastic methanogenesis as indicated by a 50 % inhibiting concentration (IC₅₀) of only 0.16 mM. Denitrifying populations were also impacted by uranium, but their sensitivity depended on the electron donor utilized. Sulfur-oxidizing denitrifiers were the least affected (IC₅₀ for denitrification activity = 0.32 mM), followed by H₂- and acetate-utilizing denitrifiers (IC₅₀ of 0.20 and 0.15 mM, respectively). In contrast, exposure to U(VI) concentrations up to 1.0 mM did not inhibit the rate of U(VI) bioreduction with H₂ as electron donor in the presence or absence of nitrate. On the contrary, a considerable increase in the uranium-reducing activity of the denitrifying and methanogenic mixed cultures was observed with increasing uranium concentrations. The results suggest that microorganisms responsible for U(V) reduction could tolerate much higher uranium concentrations compared to the other microbial populations assayed.