Intensive exploitation and transport of oil and derivatives are increasing the risk of coastal contamination by either dramatic disasters or diffuse sources. Tools for monitoring diffuse contamination, such as diesel oil that leaks from marine vessels are much needed. We experimentally tested the efficiency of antioxidant biomarkers as indicators of chronic exposure to diesel oil in a mudflat from the subtropical Bay of Paranaguá, in southern Brazil. We examined the effects of three successive diesel oil spills, with two weeks of recovery time between exposures, on the edible clam Anomalocardia flexuosa. Previous studies have highlighted its potential as a bioindicator species for diesel oil contamination in subtropical and tropical ecosystems. Endpoints measured in gill and digestive gland homogenates included the activity of antioxidant enzymes SOD, GPx, GST and levels of lipid peroxides. PAHs concentration in sediments and soft tissue were also quantified. GST and SOD were the most responsive biomarkers to the exposure. There were significant but non–cumulative departures from control levels in organisms from treated samples, which were, in all cases, more common 48 h after each experimental spill. Biomarker responses were more evident in the digestive gland than in gills. This work validated the short–term responsiveness of biomarkers as measures of repeated pulsed in situ exposure to low concentrations of diesel oil. For their routine implementation into monitoring programs for tropical estuaries our general recommendations are 1) to include several reference sites, 2) to analyze biomarker data using a logarithmic–scale and 3) to interpret deviations from “normal” activity as multiplicative interval differences.

To investigate the effects of ambient-level gas-phase peroxides concurrent with O3 on foliar injury, photosynthesis, and biomass in herbaceous plants, we exposed Japanese radish (Raphanus sativus) to clean air, 50 ppb O3, 100 ppb O3, and 2-3 ppb peroxides + 50 ppb O3 in outdoor chambers. Compared with exposure to 100 ppb O3, exposure to 2-3 ppb peroxides + 50 ppb O3 induced greater damage in foliar injury, net photosynthetic rates and biomass; the pattern of foliar injury and the cause of net photosynthetic rate reduction also differed from those occurring with O3 exposure alone. These results indicate for the first time that sub-ppb peroxides + 50 ppb O3 can cause more severe damage to plants than 100 ppb O3, and that not only O3, but also peroxides, could be contributing to the herbaceous plant damage and forest decline observed in Japan's air-polluted urban and remote mountains areas.

This study evaluated the effectiveness of a novel adsorbent (Fe(III)-AM-PGMACell), Iron(III)-coordinated amino-functionalized poly(glycidyl methacrylate)-grafted cellulose for the adsorption of arsenic(V) from aqueous solutions. The Fe(III)-AM-PGMACell was prepared through graft copolymerization of glycidyl methacrylate (GMA) onto cellulose (Cell) in the presence of N,N′-methylenebisacrylamide (MBA) as a cross linker using benzoyl peroxide initiator, followed by treatment with ethylenediamine and ferric chloride in the presence of HCl. Batch experiments were performed to evaluate the adsorption efficiency of Fe(III)-AM-PGMACell towards As(V) ions. The contact time to attain equilibrium and the optimum pH were 90 min and 6.0, respectively. More than 99.0% adsorption was achieved from an initial concentration of 25.0 mg/L. A two-step pseudo-first-order kinetic model agreed well with the dynamic behavior for the adsorption process. Equilibrium data fitted well with Sips isotherm model with maximum adsorption capacity of 78.8 mg/g at 30°C. The desorption of As(V) was achieved over 98.0% with 0.1 M NaCl solution.

The ubiquitous presence of chlorophenols (CPs) continues to be a cause of concern, owing to their recalcitrant nature. In this context, the present work investigated the degradation of model compounds, 4-chlorophenol, 2,4-dichlorophenol, 2,4,6-trichlorophenol, and pentachlorophenol, by an organic oxidant, methyl ethyl ketone peroxide (MEKP) coupled with ultraviolet irradiation in basic media. Chemical analysis was followed by high-performance liquid chromatography and gas chromatography–mass spectrometry. Despite exhibiting varied patterns of decline, chemical oxygen demand was eventually noted to decrease to the extent of up to 70 %. Simultaneous increase/decrease in the release of chloride ions and decrease in pH indicated that parallel reactions were occurring, which led to the formation of acidic reaction products. First-order dynamics was approximated for all CP congener degradation. The degraded compounds showed absolutely no presence of chlorine atoms, which was a noteworthy feature testifying to the fact that MEKP action was capable of detoxification of CP congeners.

A simple spectrophotometric method was developed to quantify chlorophenol (CP) concentrations after reaction with potassium permanganate and quenching with sodium sulfite. Other quenching agents (peroxide, sodium thiosulfate and hydroxylamine hydrochloride) were found to create absorbance in the spectral range required for CP quantification. Analysis at pH 12 gave greater absorption and sensitivity for the method compared with pH 5.6. The calibration curves of the proposed methods were linear in the concentration ranges 0.0061–0.61 and 0.0078–0.78 mM with detection limit of 0.0006 and 0.0008 mM for dichlorophenols and monochlorophenols, respectively. The oxidation kinetics of five chlorophenols in aqueous solution with excess potassium permanganate were evaluated using the analytical method. The pseudo-first-order reaction rates were found to be relatively rapid 1.42 × 10−3 to 0.024 s−1 and followed the sequence 2-chlorophenol (2-CP) > 2,6-dichlorophenol (2,6-DCP) > 4-chlorophenol (4-CP) > 2,4-dichlorophenol (2, 4-DCP) > 3-chlorophenol (3-CP). The apparent second-order rate constant was calculated from the measured pseudo-first-order rate constant with respect to CP with initial KMnO4 concentration (1.5 mM) and follows the same sequence of pseudo-first-order rate constant. This shows that chlorine atoms in the structure of chlorophenol had a significant influence on the oxidation of chlorophenols by potassium permanganate. Permanganate can be used for the treatment of chlorophenol-contaminated soil and groundwater.

Plants have immense potential for their use in the minimization of emerging environmental pollution issues. Under simulated laboratory conditions, this work investigated the growth and biochemical responses of 14-day-old cotton burdock (Arctium tomentosum Mill.) seedlings to the body burdens of multi-metals including Pb, Cu, Ni, and Zn (1.0 μM–10 mM). Biochemical traits (superoxide generation, lipid peroxidation, content of total peroxides), growth traits (axial organs growth, dry weight accumulation, leaf area), and also metal body burdens varied with types and concentrations of metals. Results indicated a significant tolerance of A. tomentosum to multi-metals that can be implicated for its potential role in the metal phytoremediation programs.

Background, aim, and scope For many years, highly concentrated wastewater generated from the pulp and paper industry has become the focus of much concern worldwide. The objectives of this study were to determine the treatment efficiency of the alkaline peroxide mechanical pulp (APMP) process wastewater using a sequencing batch reactor (SBR) and analyze the microbial dynamics of the wastewater treatment system using the random amplified polymorphic DNA (RAPD) method. Materials and methods An SBR was applied to the treatment of APMP pulp and paper process wastewater. The wastewater characteristics and many physicochemical operator indicators in the wastewater treatment process were analyzed and determined according to standard methods. Microbial 16 S rDNA in active sludge was extracted, amplified, and analyzed using the RAPD method for the microbial dynamics of the wastewater treatment system. Results and discussion Ten kinds of natural organic compounds of plants such as monoterpene were detected in the APMP pulp and paper process wastewater. With an influent chemical oxygen demand (COD) that varied in the range of 685.7 to 907.5 mg/L, the corresponding effluent COD was 176.5 to 266.1 mg/L and the removal efficiency was 70.3% to 79.8%. An optimal strain (S308: CAGGGGTGGA) was selected to study the population dynamics and diversity of the bacterial community. The RAPD-polymerase chain reaction (PCR) fingerprints showed very high polymorphism of the genetic bands (78-100%). Four groups of species were clustered using the unweighted pair group method with arithmetic (UPGMA) analysis, and the genetic distance was close between the species within each group. The Shannon-Weaver index was high and varied over time with the COD removal. Conclusions The RAPD-PCR technique can be used to study microbial dynamics, which was shown to vary over time with the removal efficiency of SBR treating APMP pulp and paper process wastewater.

The study mainly focuses on surface properties to investigate the deactivation factors of Pt/MnO ₓ -CeO₂ by H₂ temperature-programmed reduction, CO chemical adsorption, NO ₓ -temperature-programmed desorption (TPD), O₂-TPD, NO temperature-programmed oxidation, SEM, TEM, in situ diffuse reflectance infrared Fourier transform spectra, Raman, and thermogravimetric methods. The results show that there are three main factors to lead to hydrothermal deactivation of the catalyst: redox property, oxygen vacancy, and surface nitrates. The loss of oxygen vacancies decreases the generation and desorption of active oxygen and that of surface nitrates weakens the production of NO₂ and surface peroxides (-O₂⁻). These factors greatly result in the damage of the C-NO₂-O₂ cooperative reaction.

Recent offshore petroleum exploration has increased the risks of oil spills worldwide. We investigated biomarker responses to diesel oil exposure in two tropical and subtropical species, the clam Anomalocardia flexuosa and the polychaete Laeonereis culveri. Animals were exposed to oil-spiked sediment at two different concentrations (0.5 L and 1.0 L m⁻²). Activities of antioxidant enzymes catalase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GPx); glutathione transferase (GST); and lipid peroxides (LPO) were assessed in bivalve digestive glands and polychaete whole-body homogenates at 36 and 60 h of exposure. Significant variation in enzymatic antioxidant activity depended on the sampling time after exposure. No similar response patterns, either increases or decreases, were detected for the two target species, and biomarker responses were species-specific. L. culveri showed clearer patterns in its antioxidant response and should be prioritized over other species in biomonitoring studies involving oil exposure. Understanding the temporal variability of these biomarkers is a necessary action before implementing them as indicators measures in oil contamination biomonitoring programs. Our results provide a better understanding of biomarker responses in subtropical species, evidencing their potential use as sentinels of oil contamination.

Transition-metal is known to catalyze peroxymonosulfate (PMS) decomposition to produce sulfate radicals. Here we report reactions between PMS and chloride, without a need of transition metals, also can be used to degrade organic dye pollutant (Rhodamine B, (RhB)). Some important operating parameters, such as dosages of PMS and Cl(-), pH of solution, temperature, ionic strength, and several common cations, were systematically investigated. Almost complete decoloration of RhB was achieved within 5 min ([PMS] = 0.5 mM, [Cl(-)] = 120 mM, and pH 3.0), and RhB bleaching rate increased with the increased dosages of both PMS and chloride ion, following the pseudo-first-order kinetic model. However, the total organic carbon (TOC) removal results demonstrated that the decoloration of RhB was due to the destruction of chromophore rather than complete degradation. RhB decoloration could be significantly accelerated due to the high ionic strength. Increasing of the reaction temperature from 273 K to 333 K was beneficial to the RhB degradation, and the activation energy was determined to be 32.996 kJ/mol. Bleaching rate of RhB with the examined cations increased with the order of NH4 (+) < Na(+) < K(+) < Al(3+) < Ca(2+) < Mg(2+). Some major degradation products of RhB were identified by GC-MS. The present study may have active technical implications for the treatment of dyestuff wastewater in practice.