Soil is a primary resource used by mankind to ensure its needs mainly through agriculture. Its sustainability is regulated by the indigenous organisms it contains such as microorganisms. Current agricultural practices employ mixtures of pesticides to ensure the crops yield and can potentially impair these non-target organisms. However despite this environmental reality, studies dealing the susceptibility of microorganisms to pesticide mixtures are scarce. In this context, we designed a 3-month microcosm study to assess the ecotoxicity of realistic herbicide mixtures of formulated S-metolachlor (Dual Gold Safeneur®), mesotrione (Callisto®), and nicosulfuron (Milagro®) on the abundance, the diversity, and the activities of microorganisms from a “clay/organic matter-rich” soil, with a particular attention given to N-cycle communities. These communities appeared to be quite resistant to realistic mixtures even if transient effects occurred on the N-cycle-related communities with an increase of ammonification and an inhibition of nitrification as a short-term effect, followed by an increase of denitrification and an accumulation of nitrates. As nitrates are known to be highly leachable with a strong pollution potential, intensive studies should be carried out at field level to conclude on this potential accumulation and its consequences. Moreover, these data now need to be compared with other agricultural soils receiving these herbicide mixtures in order to bring general conclusion on such practices.

The paper presents a comprehensive analysis of the most basic features of the air quality of a Mediterranean urban environment area. The impact of meteorology on the air quality is also examined. Observational surface concentrations of the most important air pollutants, recorded at two measuring stations in Patras, Greece, are used. The Weather Research and Forecasting (WRF) meteorological model was employed to produce a series of surface and upper air data and local circulation and ventilation indices. These modeled data along with selected surface meteorological observational data comprise a substantial data set that was used to assess the effect of meteorology on the air quality. Mostly during the summer period, a significant proportion of the particulate matter is transported from sources away from the measuring sites. The synoptic setting of winter and summer seasons represented primarily by the local ventilation and recirculation, the wind, the boundary layer height, and the precipitation has a very strong impact in the overall formation of the air quality status.

In this study, nanosized zero-valent iron-reduced graphene oxide (nZVI-rGO)-activated persulfate (PS) was used to investigate the generation of reactive oxygen species (ROS) for the degradation of trichloroethylene (TCE) in the aqueous solution. More than 98 % of TCE was degraded within 2 min under experimental conditions. The generation of ·OH increased when the pH was shifted toward the basic region while ·SO₄⁻ radicals’ intensity increased in the acidic pH. Different scenarios have been observed in ·O₂⁻ generation in the neutral and strong basic pH and decreased in acidic or slightly basic pH. In addition, the intensity of ·OH was increased with the addition of HCO₃⁻ (10 mM) and NO₃⁻ (100 mM) but decreased in the presence of Cl⁻ (10 and 100 mM), HCO₃⁻ (100 mM), and NO₃⁻ (10 mM). The degradation of anisole, probe for both ·OH and ·SO₄⁻, was slightly enhanced by 10 mM NO₃⁻ anions but decreased in 100 mM salt solution. ·O₂⁻ intensity was increased while HCO₃⁻ (10 and 100 mM) and NO₃⁻ (100 mM) anions were used. nZVI-rGO-activated PS process could remove TCE in aqueous effectively, and the ROS generation and intensity were influenced by solution pH values and anions.

Sugarcane molasses, which is a kind of microbial carbon source, is a viscous by-product of the refining of sugarcane into sugar. However, experiments were designed to ascertain the mechanism and kinetics of Cr(VI) reduction with sugarcane molasses without adding microbes in aqueous solution. Results indicated that sugarcane molasses can reduce Cr(VI) to Cr(III) at pH values that range from 2.0 to 6.1 when no bioreduction occurs in the reaction. Furthermore, the reaction mechanism was proven to be that Cr(VI) acts as an electrophile that readily accepts electrons from the phenolic hydroxyl group of plant polyphenol, and it is then reduced to Cr(III) and in the process oxidizes the phenolic hydroxyl group to a quinone. Meanwhile, the reaction could be described by the pseudo-first-order kinetic model with respect to Cr(VI) concentration. The reaction rate constants were 324.2, 65.9, 21.9, and 14.4 h⁻¹ when pH values were 2.0, 3.5, 5.0, and 6.1, respectively, at 20 °C. The k ₒbₛ increased 3.36, 7.02, and 13.48 times with the temperature adjusted from 5 to 10, 20, and 30 °C.

Alkyl polyglucosides, due to their low toxicity and environmental compatibility, could be used in biodegradation of hydrophobic compounds. In this study, the influence of Lutensol GD 70 on the cell hydrophobicity and zeta potential was measured. The particle size distribution and surfactant biodegradation were also investigated. Microbacterium sp. strain E19, Pseudomonas stutzeri strain 9, and the same strain cultivated in stress conditions were used in studies. Adding surfactant to the diesel oil system resulted in an increase of the cell surface hydrophobicity and the formation of cell aggregates (a high polydispersity index). The correlation between cell hydrophobicity and zeta potential in examined samples was not found. The results showed a significant influence of Lutensol GD 70 on the changes in cell surface properties. Moreover, a high biodegradation of a surfactant (over 50 %) by tested strains was observed. The biodegradation of Lutensol GD 70 depends on the length of both polar and nonpolar chains. A long-term contact with diesel oil of stressed strain modifies not only cell surface properties but also its ability to a surfactant biodegradation.

The capability of W⁶⁺-impregnated ZnO photocatalysts for sunlight mineralization of a variety of structurally different dyes has been investigated. Compared to bare ZnO, the W⁶⁺-loaded photocatalysts showed significantly higher activity for the decolorization as well as mineralization of dyes, and complete mineralization was noticed in a short span of 150 min. The results obtained by various analytical tools were correlated to estimate the mechanistic aspects of the decolorization/mineralization process and to identify the nature of the oxidizing species involved in the process. A strong dependence of the decolorization/mineralization process was observed on the nature and number of auxochromes attached to color-generating conjugated system. The rapid decolorization/mineralization of the dyes and release of corresponding anions with the decolorization of dyes suggested the involvement of charged rather than radical reactive oxygen species (ROS) in the oxidation process. Langmuir-Hinshelwood kinetic model was found to be best suited for evaluating the kinetics of mineralization process. The effectiveness of the catalysts for the decolorization/mineralization of a mixture of dyes was also examined. The suitability of the catalysts for successive use in sunlight exposure was also evaluated.

The degradation of hexachlorobenzene (HCB) is of great concern and attracts considerable scientific and regulatory interests, due to the high toxicity, great bioaccumulation, and persistence of HCB in the environment. However, in the real HCB-contaminated soil, the effect of coexisting chlorobenzene congeners on the degradation capacity of HCB is poorly known. In this work, the anaerobic degradation behaviors of three coexisting chlorobenzene congeners pentachlorobenzene (PeCB), 1,2,4,5-tetrachlorobenzene (1,2,4,5-TeCB), and 1,2,4-trichlorobenzene (1,2,4-TCB) and the influence of initial pH and reaction temperature on the dechlorination of HCB in HCB-contaminated soil from the dye plant were studied. The amount and extent of accumulated coexisting chlorobenzenes was analyzed under different environmental conditions. The results indicate that the concentrations of three coexisting chlorobenzene congeners change in the form of wave. The anaerobic degradation activity of HCB is reduced due to the feedback inhibition caused by accumulation of coexisting chlorobenzene congeners, and the feedback inhibition varies from environmental conditions.

Concentrated animal feeding operations (CAFOs) are the principal means of livestock production in the USA and Europe, and these industrial-scale facilities have a high potential to pollute nearby waterways. Chemical and biological stream water quality of a swine and poultry CAFO-rich watershed was investigated on 10 dates during 2013. Geometric mean fecal coliform counts were in the thousands at five of seven sites, especially in locations near swine waste sprayfields. Nitrate concentrations were very high and widespread throughout the watershed, with some individual samples yielding >10 mg-N/L. Ammonium concentrations were likewise high, but greatest near swine waste sprayfields, ranging up to 38 mg-N/L. Five-day biochemical oxygen demand (BOD5) concentrations exceeded 10 mg/L in 11 of 70 stream samples, reaching as high as 88 mg/L. BOD5 concentrations were significantly correlated with components of animal waste including total organic carbon, ammonium, and phosphorus, as well as the nutrient response variable chlorophyll a. The degree of nutrient and fecal contamination did not significantly differ between rainy and dry periods, indicating that surface and groundwater pollution occurs independently of stormwater runoff. This research shows that industrial-scale swine and poultry production leads to chronic pollution that is both a human health and ecosystem hazard. There are approximately 450,000 CAFOs currently operating in the USA, with the majority located in watersheds feeding major riverine and estuarine systems with known water quality problems. Current US waste management protocols for this widespread system of livestock production fail to protect freshwater and estuarine ecosystems along the US Mid-Atlantic, Southeast and Gulf coasts, and expansion into industrializing nations will likely bring severe pollution with it.

Continuous use of recycled water (treated sewage effluent) over a long period of time may lead to the accumulation of salt in the root zone soil. This is due to the relatively higher levels of salt content in the recycled water compared to surface water. In this study, a laboratory column study was carried out to validate the HYDRUS 1D model under no rain condition. During the validation, the relative error and the % bias between observed and simulated soil water electrical conductivity (ECSW) were found to be low and varied in a range of 5–10 and 5–6 %, respectively. The validated model was then used to predict long-term (5 years) salt accumulation under drought conditions. The analysis of model predicted salt values showed a cyclical pattern of salt accumulation in the root zone, and this related to the variation in rainfall and evapotranspiration. The mean root zone ECSWin the 5th year was found to be within the highest salinity tolerance threshold for pasture (11.2 dS/m); however, the maximum root zone ECSWwas found to be about 63 % more than the threshold. Irrespective of seasons, in 5 years time, ECSWat the depth of 1.0 m increased from 3.0 to 7.0 dS/m, which may pose a salinity risk to the groundwater table if there is a perched water table at a depth <1 m below the field surface. One of the management options to minimise long-term salt accumulation was also examined. By reducing the salt in recycled water by 50 %, it was possible to keep the ECₛwwithin the recommended threshold values. Overall, the methodology developed in this study can be used to identify appropriate management options for sustainable recycled water irrigation.

Four kinds of surfactants were used to increase accessibility of pyrene and cadmium (Cd) in simulated pyrene, Cd, and pyrene-Cd soils in this study. Tea saponin (TS) at 40 mg L⁻¹groups (exchangeable fraction of Cd and bioaccessible fraction of pyrene were 8.96 and 36.93 mg kg⁻¹) showed more preferable potential application in improving solubilization capability than other surfactants. The morphology of Cd was transformed from Fe-Mn oxides (8.86 to 7.61 and 8.67 to 7.99 mg kg⁻¹in Cd and pyrene-Cd soil) and associated to carbonates fractions (4.46 to 4.36 and 4.28 to 4.36 mg kg⁻¹in Cd and pyrene-Cd soil) to exchangeable fraction with adding TS. These two morphological changes were important processes in the solubilization of Cd. The morphology of pyrene was transformed from associated fraction (72.15 to 61.95 and 71.02 to 63.48 mg kg⁻¹in pyrene and pyrene-Cd soil) to bioaccessible fraction (26.66 to 33.71 and 26.91 to 36.93 mg kg⁻¹in pyrene and pyrene-Cd soil) with adding TS. This morphological transformation was important in the improving of solubilization capacity of pyrene. In contrast, the solubilization of pyrene was promoted in the presence of Cd in pyrene-Cd soil (the bioaccessible fractions were 33.71 and 36.93 mg kg⁻¹in pyrene and pyrene-Cd soil), but the solubilization of Cd was hindered in the presence of pyrene (the exchangeable fractions of Cd were 8.86 and 8.67 mg kg⁻¹in Cd and pyrene-Cd soil). These findings will be beneficial for application of surfactants in soil remediation.