Mercury is considered a ubiquitous, toxic, and global pollutant. In this study, ambient Total Gaseous Mercury (TGM) concentrations over the South African Highveld are characterised. Studies on ambient mercury in this region is important because of various anthropogenic emission sources. In this pilot study, concentrations of TGM and criteria pollutants (O3, SO2, NO, NO2, and CO) were measured concurrently with meteorological parameters at Balfour (BF), Middelburg (MB), and Standerton (ST) from January 2009 to December 2009. The spatial variation of TGM concentrations ranged from 0.40 to 28.72 ng/m3 (1.99 0.94 ng/m3), 0.12–9.91 ng/m3 (1.04 0.62 ng/m3), and 0.21–32.10 ng/m3 (1.25 1.38 ng/m3), at BF, MB, and ST, respectively. Generally, concentrations fell within the Northern Hemisphere background range of 1.5–1.7 ng/m3 and Cape Point, South Africa background of 1.2–1.4 ng/m3, with the exception of outliers. The outliers were much higher than the background values and may be the result of pollution events. Seasonal variation varied with descending orders of summer, spring, winter, autumn, at BF; summer, winter, autumn, spring at MB; and winter, spring, summer at ST (no data available for autumn). This study observed no profound diurnal patterns at BF and MB where sparse local and regional sources appear to have been the predominant sources. An interesting phenomena, however, was observed at ST where the diurnal cycle suggests a potential significant influence from local domestic combustion sources.

The air-water exchange of polycyclic aromatic hydrocarbons (PAHs) is an important process in determining the fate, transport and chemical loadings of these contaminants in the atmosphere and water bodies. Concentration levels of PAHs in air (gaseous and particulate) and surface water were investigated in the environments of two polluted lagoons along the eastern coast of the Red Sea to study air water exchange and dry deposition fluxes. Nine priority parent PAHs and nine methylated PAHs were identified and quantified by GC-MS. The range of total PAHs in surface water was from 120.29 ng L⁻¹ to 524.45 ng L⁻¹ (average: 308.7 ng L⁻¹, n = 19). The PAHs levels in air recorded significant rise form the previous study. The probable sources of dissolved PAHs in water were found predominantly to be of petrogenic origin in one lagoon and of pyrogenic origin in the other lagoon. The dry deposition fluxes for individual congeners ranged between 0.01 ng m⁻²d⁻¹ to 2.82 μg m⁻²d⁻¹. After Henry's law constant corrections for temperature and salinity; the air-water exchange fluxes were found in the range of −9.7 × 10⁴ to 8.6 × 10⁶ ngm⁻²d⁻¹ with an average of 6.8 × 10⁵ ngm⁻²d⁻¹. Beside the other sources of PAHs in the studied lagoons, high temperature and wastewater dumping might affect the magnitude and direction of air-water exchange fluxes.

Speciated VOCs and regulated air pollutant emissions (CO, HC and NO) of carburetor (CB) and fuel injection (FI) motorcycles were evaluated based on engine dynamometer tests. Effects of engine loads and emission control systems were evaluated. CB was equipped with oxidation catalytic converter (OCC) and secondary air system (SAS) while FI had three-way catalytic converter (TWC) and oxygen sensor (OS). Under normal operation of the control devices, the emissions of regulated pollutants and the sum of detected VOCs (ΣVOC) were higher in CB than in FI motorcycle. Alkanes and aromatics had the highest concentrations contributing approximately 90% to the ΣVOC while xylene and toluene were most abundant among the BTEX, in both motorcycles. Emissions of all regulated pollutants and ΣVOC increased with increase in engine load. The emission control devices showed differential efficiencies on different VOC groups. Average emission reduction efficiencies of OCC with SAS (CB motorcycle) were 45.4% (ΣVOC) and 48.6% (BTEX) and TWC with OS (FI motorcycle) were 74.4% (ΣVOC) and 88.0% (BTEX). Without SAS, the efficiency of OCC dropped to 30.2% (ΣVOC) and 34.9% (BTEX) in CB motorcycle. Similarly, the efficiency of TWC reduced to 69.0% (ΣVOC) and 85.2% (BTEX) when the OS was blocked in FI motorcycle. The ozone formation potentials of VOCs ranged from 500 mg-O3/m3 (FI motorcycle with TWC and OS, TO 20%) to 2218 mg-O3/m3 (CB motorcycle without control system, TO 30%).

Abstract: The cryosphere in South America is a very important resource because it is the main source of water for 85 million inhabitants distributed in Colombia, Ecuador, Peru, Bolivia, Chile and Argentina [1-2]. To know the effects due to global phenomena such as arctic oscillation (AO) in the reduction of the cryosphere in this region, we proceeded to analyze sources of reanalysis information (ERA-40; NCEP/NCAR Reanalysis) and high resolution snow cover (MOD10 500m) from Moderate-Resolution Imaging Spectroradiometer (MODIS). Several linear adjustments were made to observe how snow cover variations (Y) responded to variations in AO (X1 ), surface temperature (X2 ) and snow precipitation (X3 ).

Human health and well-being are strongly linked to the state of the environment. The high industrial pressure present in the Province of Brescia, located in Northern Italy, produced strong environmental and health concerns. This narrative review of the literature aims at identifying the studies focused on the association between exposure to environmental pollutants and health effects in the population living in this area. Thirteen papers fitted the inclusion criteria: five were focused on the connection among pollutants present in air matrix and health effects, seven on both air and soil, and one on soil. No study investigated the relationship with water pollution. The great variability in the analyzed end-points made it difficult to draw precise conclusions, but the fact that, in almost all the studies, the investigated health effects have a positive association with the exposure to different kinds of pollutants, allows us to hypothesize that the considered population is living in an area where the “environmental pressure” could produce significant health effects in the future.

N-nitrosodimethylamine (NDMA), a toxic disinfection byproduct commonly associated with chloramination, has recently been found to form from an anti-yellowing agent (4,4′-hexamethylenebis (1,1-dimethylsemicarbazide) (HDMS)) during ozonation but the mechanisms are unclear. In this paper, the potential roles of molecular ozone (O₃) and hydroxyl radical (∙OH) on NDMA formation from HDMS were investigated under various oxidation conditions (ozone dosages, pH) and different components in water (bromide ion (Br⁻), bicarbonate ion (HCO₃⁻), sulfate ion (SO₄²⁻), and humic acid (HA), as well as natural organic matter (NOM) from a lake). Moreover, HDMS transformation pathways by ozonation were determined. The results indicated that the formation of NDMA was enhanced through the combined effect of O₃ and ∙OH compared to that by O₃ alone (addition of tert-butyl alcohol (tBA) as ∙OH scavenger). ∙OH itself cannot generate NDMA directly; however, it can transform HDMS to intermediates with higher NDMA yield than parent compound. The NDMA generation was affected (small dosages promoted but high dosages inhibited) by HA or Br⁻ no matter with or without tBA. The presence of SO₄²⁻ and HCO₃⁻ ions lowered NDMA formation through ∙OH scavenging effect. Increasing pH not only increased degradation rate constant by enhancing ∙OH generation but also affected HDMS dissociation ratio, reaching the maximum NDMA formation at pH 7–8. Natural constituents in selected water matrix inhibited NDMA formation. Impacts of these influencing factors on NDMA formation by only O₃ however were significantly less pronounced over that by the joint roles of O₃ and ∙OH. Based on the result of Q-TOF, LC/MS/MS, and GC/MS, the possible transformation pathways of HDMS by ozonation were proposed. The NDMA enhancement mechanism by the combined effect of O₃ and ∙OH can be attributed to greater amounts of intermediates with higher NDMA yield (such as unsymmetrical dimethylhydrazine (UDMH)) produced. These findings provide new understanding of NDMA formation upon ozonation of typical amine-based compounds.

Selenium (Se) is a vital element which leads to strong antioxidation in animals and humans. However, the mechanism underlying natural cereal Se–induced biological changes is not well understood. This study intended to explore the gene differential expression in naturally aged mice exposed to selenium by RNA-Seq technique. A total spectrum of 53 differentially expressed genes was quantified in mice heart tissues treated with Se-rich and general rice. The GO functional annotation of differentially expressed genes disclosed the enrichment of cellular process, ionic binding, biological regulation, and catalytic activity. One hundred twenty-three differential pathways (cardiovascular diseases, immune system, transport and catabolism, longevity regulating, and PI3K-AKT signaling) were identified according to KEGG metabolic terms. Afterwards, the effect of Se-rich rice on the antioxidant activity was assessed. The selenium-rich diet increased the total antioxidant capacity (T-AOC), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) in mice serum and livers while significantly reduces methane dicarboxylic aldehyde (MDA) contents. FOXO1 and FOXO3 genes, which acted as the regulators of apoptosis and the antioxidant enzyme, were significantly enhanced in mice when fed with Se-rich rice. In short, the present findings disclosed the alluring insights of organic and inorganic selenium sources on certain biological processes and antioxidant activity of living bodies. However, long-term trials are still required to draw a definitive conclusion, including risks and benefit analysis for various management strategies.

Uranium wastewater treatment has been performed by adsorption method using Mg(OH)₂-impregnated activated carbon. Research purposes are to determine (i) uptake capacity of the adsorption isotherm of uranium in Mg(OH)₂-impregnated activated carbon, (ii) mathematical correlation of uranium (VI) adsorption rate, and (iii) effect of the impregnation ratio of adsorbent to uranium removal efficiency. Adsorbent was synthesized through several stages, i.e., pyrolysis of coconut shell (400 °C), chemical activation using NaOH, and impregnation process using varied solutions of MgCl₂ (600 °C). The materials were characterized comprehensively using FTIR, BET, XRF, and XRD. The parameters studied in this research were adsorption temperature (T), average particle diameter of adsorbent (d), mass ratio of adsorbent to wastewater solution (r), and impregnation ratio of Mg(OH)₂/activated carbon. The results shown that equilibrium data are well fitted with the Langmuir isotherm model with the maximum adsorption capacity about 85 mg/g at 303 K and dimensionless constant separation factor (RL) value about 0.7. The adsorption rate was increased by increasing the adsorption temperature, mass ratio of adsorbent to wastewater solution, and the decrease of particle diameter of adsorbent with mathematical equation of the uranium (VI) adsorption rate as:[Formula: see text]In addition, the results also shown that increasing the impregnation ratio from 0.3 to 1.0 can increase the uranium removal efficiency up to 67.3%.

A growing number of electrochemical oxidation system was employed for the degradation of refractory contaminants. In this study, a boron-doped diamond (BDD) anode/Ti cathode equipped in the differential column batch reactor (DCBR) was utilized for electrochemical oxidation of ciprofloxacin (CIP). The feed solution within the DCBR system was confirmed as a uniform flow state through a computational fluid dynamics (CFD) simulation analysis. The results showed that the BDD anode/Ti cathode electrochemical system was with a high efficiency oxidation performance when treating the CIP contaminant. The CIP was completely degraded within 20 min, and over 50% DOC removed after 120 min. Therefore, two-stage electrochemical oxidation mechanism was proposed. Four major factors, the initial concentration, current density, pH, and electrolyte concentration, on the CIP degradation efficiency were systematically investigated. The CIP degradation curve followed pseudo first-order degradation kinetics. The electric efficiency per order (EE/O) of the electrochemical oxidation system was calculated to determine an optimal operation condition. Moreover, the oxidation intermediates were identified with a mass spectrometry (LC/MS/MS) and the degradation pathways were proposed in this study. The destruction of quinolone moiety and piperazine ring and fluorine substitution were the three possible degradation pathways during BDD anode oxidation process.

Cyproconazole is a triazole fungicide used to protect a diverse range of fruits, vegetables, and grain crops. As such, it has the potential to enter aquatic environments and affect non-target organisms. The objective of this study was to assess the acute toxicity of the triazole fungicide cyproconazole to zebrafish embryos by assessing mortality, developmental defects, morphological abnormality, oxidative respiration, and locomotor activity following a 96-h exposure. Zebrafish embryos at 6-h post-fertilization (hpf) were exposed to either a solvent control (0.1% DMSO, v/v), or one dose of 10, 25, 50, 100, 250, and 500 μM cyproconazole for 96 h. Data indicated that cyproconazole exhibited low toxicity to zebrafish embryos, with a 96-h LC₅₀ value of 90.6 μM (~ 26.4 mg/L). Zebrafish embryos/larvae displayed a significant decrease in spontaneous movement, hatching rate, and heartbeats/20 s with 50, 100, and 250 μM cyproconazole exposure. Malformations (i.e., pericardial edema, yolk sac edema, tail deformation, and spine deformation) were also detected in zebrafish exposed to ≥ 50 μM cyproconazole, with significant increases in cumulative deformity rate at 48, 72, and 96 hpf. In addition, a 20–30% decrease in basal and oligomycin-induced ATP respiration was observed after 24-h exposure to 500 μM cyproconazole in embryos. To determine if cyproconazole affected locomotor activity, a dark photokinesis assay was conducted in larvae following 7-day exposure to 1, 10, and 25 μM cyproconazole in two independent trials. Activity in the dark period was decreased for zebrafish exposed to 25 μM cyproconazole in the first trial, and hypoactivity was also observed in zebrafish exposed to 1 μM cyproconazole in a second trial, suggesting that cyproconazole can affect locomotor activity. These data improve understanding of the toxicity of cyproconazole in developing zebrafish and contribute to environmental risk assessments for the triazole fungicides on aquatic organisms. We report that, based on the overall endpoints assessed, cyproconazole exhibits low risk for developing fish embryos, as many effects were observed above environmentally-relevant levels.