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During the stable operation stage of the BF-MPBRs, the reduction in dissolved inorganic nitrogen (DIN), dissolved inorganic phosphorus (DIP), sulfadiazine (SDZ), sulfamethazine (SMZ) and sulfamethoxazole (SMX) were found in the range of 91.0-99.6%, 92.1-98.4%, 61.0-79.2%, 50.0-76.7% and 60.8-82.1%, respectively. Therefore, nutrient and SAs were simultaneously and efficiently removed from marine aquaculture wastewater by microalgae cultivation in BF-MPBR. Karst systems, as well as springs, are vulnerable to water perturbation brought by infiltration. In this research, sources of water perturbations were examined. The first objective is to provide a method that can determine the origin of the water flowing in the karst outlet. The second objective is to identify the associated water quality hazards caused by the infiltration source. The method relies on these parameters turbidity, DOC, NO3-, particle size, and bacteria (E. coli, enterococcus and total coliforms). As the method was applied during flood events, measurement of the water flow is also needed to have a basic knowledge on the hydrodynamic of the water resource. The proposed method is based on a high resolution monitoring of physico chemical parameters of the water flowing during flood events. Using this proposed method, (1) the origin of the water can be identified, (2) the type and nature of water perturbation can be described, and (3) the type of water perturbation that accompanies contaminants suchation obtained can be used as a basis in forecasting and planning the management actions or water quality treatments needed. Microbial electro-Fenton system (MEFS) shows potential application for degradation of recalcitrant pollutants. In order to simplify the MEFS and adapt to the practical application situations, such as water, soil or sludge remediation, we developed an automatic MEFS (AMEFS) for degradation of a recalcitrant dye, acid orange 7. The AMEFS contained a microchannel-structured carbon decorated with iron oxides as electro-Fenton cathode. The AMEFS could be either two-electrode configuration that the microchannel-structured carbon connected with an additional bioanode by an external circuit, or single-electrode configuration that the microchannel-structured carbon served as both bioanode and cathode. Thanks to the microchannel structure of the carbon cathode, the AMEFS could be auto-driven by a process similar to the transpiration process of natural plants. learn more The two-electrode AMEFS had higher degradation efficiency of acid orange 7 at lower external resistance, and achieved the highest degradation efficiency of 96% at the short-circuit condition. The single-electrode configuration simplified the setup of the AMEFS and possessed comparable performance with that of two-electrode configuration at short-circuit condition. Moreover, it could degrade high concentration acid orange 7 of up to 50 mg L-1 and achieve a high degradation efficiency of over 93%. The AMEFS could be applied for soil and sludge remediation by direct insertion of the microchannel structured carbon into contaminated body. V.Smoke from wildfires contains many air pollutants of concern and epidemiological studies have identified associations between exposure to wildfire smoke PM2.5 and mortality and respiratory morbidity, and a possible association with cardiovascular morbidity. For this study, a retrospective analysis of air quality modelling was performed to quantify the exposure to wildfire-PM2.5 across the Canadian population. The model included wildfire emissions from across North America for a 5-month period from May to September (i.e. wildfire season), between 2013 and 2015 and 2017-2018. Large variations in wildfire-PM2.5 were noted year-to-year, geospatially, and within fire season. The model results were then used to estimate the national population health impacts attributable to wildfire-PM2.5 and the associated economic valuation. The analysis estimated annual premature mortalities ranging from 54-240 premature mortalities attributable to short-term exposure and 570-2500 premature mortalities attributable to long-term exposure, as well as many non-fatal cardiorespiratory health outcomes. The economic valuation of the population health impacts was estimated per year at $410M-$1.8B for acute health impacts and $4.3B-$19B for chronic health impacts for the study period. The health impacts were greatest in the provinces with populations in close proximity to wildfire activity, though health impacts were also noted across many provinces indicating the long-range transport of wildfire-PM2.5. Understanding the population health impacts of wildfire smoke is important as climate change is anticipated to increase wildfire activity in Canada and abroad. Nitrous oxide (N2O) is an important greenhouse gas contributing to global climate change. Emissions of N2O from acidic forests are increasing rapidly; however, little is known about the mechanisms driving these emissions. We analyzed soil samples from a high N2O emission area (HEA, 224-601 μg N m-2 h-1) and an adjacent low emission area (LEA, 20-30 μg N m-2 h-1) of a highly acidified forest. HEA showed similar carbon and nitrogen (N) pools and microbial biomass to LEA, but significantly higher moisture and extractable nutrients than LEA did. GeoChip 4 detected 298 gene families (unadjusted P  less then  0.05; 94, adjusted P  less then  0.05) showing significantly different structures between HEA and LEA. Both areas had highly diverse N cycling functional genes. However, HEA had higher relative abundances of nor, P450nor, and archaeal nitrifier nirK, which provided evidence for the importance of denitrifiers in N2O emission. HEA also showed significantly higher relative abundances of lignin- and cellulose-degrading genes, oxygen-limitation-response genes and denitrifier ppk, but lower abundances of N- and phosphorus (P) -limitation-response genes especially denitrifier pstS, corresponding to the higher moisture and extractable nutrients conducive to denitrification. The moisture, extractable nutrients and pH explained over 50% variation in microbial communities, and extractable P appeared as the key factor driving community variation and consequently regulated N2O production. CAPSULE ABSTRACT N2O emission in highly acidified forest soils was related to the diverse N functional genes, especially denitrification genes, and was affected by soil properties. In this study, an intrinsic kinetics model was proposed to simulate the adsorption process. The kinetics model was established based on the collision theory, where the available adsorption site and residual adsorbate concentration were considered. The model specifically highlights the significance of initial conditions in its equation. The initial reaction condition is expressed by the model parameter ξ, which includes four factors concentration, volume, adsorbent dosage and adsorption capacity. The applicability of this model was mainly explored with the phosphate adsorption process by layered double hydroxides (LDH). Experimental results indicate that, at a certain initial condition, the intrinsic kinetics rate coefficient exhibits a superior stability, making the adsorption rate become comparable among different materials. On this basis, the kinetics rate coefficients of 60 materials were compared, and the LDH was proved to be advantageous in phosphate removal rate. Additionally, the intrinsic kinetics model was successfully applied to predict the phosphate adsorption kinetics under a wide range of initial conditions. The predicted concentration throughout the entire adsorption process is well consistent with the evolution of experimental data. This model is an effort to advance the kinetics analysis from fitting to comparison and prediction. Fipronil and its metabolites are potentially harmful to the ecological environment and have chronic neurotoxic effects, which makes it to be classified as class C carcinogens. Fipronil has been banned from agricultural use in China since 2009, but its residue remains in the environment. Therefore, an efficient and economical method is urgently needed to degrade fipronil residues in the environment. Herein, the degradation of fipronil in water solution using argon microwave-induced plasma (MIP) system was studied and a plausible reaction pathway was proposed in combination with Density Functional Theory (DFT) calculations. The degradation of fipronil by MIP system was optimized in terms of input power, plasma-sample distance, initial concentration and gas flow rate. After short time MIP treatment with an input power of 150 W, as high as 85.62% degradation efficiency was achieved for the fipronil at concentration of 20 mg·L--1 under the optimized conditions, and the corresponding energy efficiency was 1334.8 mg·kwh-1. Optical emission spectrometry (OES) was employed to characterize the distribution and intensity of OH, H and O species which play key roles in the degradation of fipronil by plasma, and it revealed that the degradation reaction mainly occurs at gas-liquid interface where the highest intensity of OH, H and O species was observed. High resolution mass spectrometric analysis in combination quantum chemical calculations indicate that a wide diversity of reaction processes occurred for fipronil degradation under MIP treatment, involving oxidation or reduction, nitro reduction, oxidative dichlorination, reductive dichlorination, hydration, dehydration and thiourea to urea. The possible degradation mechanism and pathways were proposed based on the degrading species identified by high resolution Mass Spectrometry (HRMS) and the thermodynamic profiles. The occurrence of nanoplastics in oceans' surface waters is no more a hypothesis and it could severely affect marine organisms from different trophic levels. Nanoscale particles interaction with dissolved natural organic matter (NOM) significantly influence their behaviour and consequently bioavailability and toxicity to marine species. Extracellular polymeric substances (EPS) are among the main components of the NOM pool in seawater yet have been so far little investigated for their effect in altering the physical-chemical properties of nanosized objects. Here we employed EPS from marine diatom Phaeodactylum tricornutum to study the evolution of an eco-corona formation upon incubation with 60 nm carboxylated polystyrene nanoparticles (PS-COOH NPs), as proxy for nanoplastics in seawater. EPS significantly reduced PS-COOH NPs aggregation rate compared to biomolecule free natural seawater (NSW) and caused the formation of complexes constituted by both carbohydrate and protein components. Size Exclusion Chromatography (SEC) revealed four main distinct groups of peaks, spanning from high (>100 kDa) to low molecular weight (20 kDa) molecules, characterized by a high chemical heterogeneity. The lowering of the chromatographic signals detected after EPS incubation with PS-COOH NPs, mainly in the eluates at high molecular weight, suggests that an important fraction of EPS remained adsorbed on PS-COOH NPs. In agreement, SDS-PAGE analysis of proteins adsorbed on PS-COOH showed the occurrence of an eco-corona formed by proteins in the range of molecular weight 30-100 kDa. No toxicity to diatoms was observed upon PS-COOH exposure (72 h, 1-100 mg L-1) even by adding a further source of exogenous EPS during exposure. Moreover, the addition of EPS reduced ROS production, even when cells were incubated with PS-COOH NPs at 10 and 50 mg L-1, suggesting an antioxidant scavenging activity of EPS.