Methanotrophs not only play an important role in mitigating CH₄ emissions from the environment, but also provide a large quantity of CH₄-derived carbon to their habitats. In this study, the distribution of CH₄-derived carbon and microbial community was investigated in a consortium enriched at three O₂ tensions, i.e., the initial O₂ concentrations of 2.5 % (LO-2), 5 % (LO-1), and 21 % (v/v) (HO). The results showed that compared with the O₂-limiting environments (2.5 and 5 %), more CH₄-derived carbon was converted into CO₂ and biomass under the O₂ sufficient condition (21 %). Besides biomass and CO₂, a high conversion efficiency of CH₄-derived carbon to dissolved organic carbon was detected in the cultures, especially in LO-2. Quantitative PCR and Miseq sequencing both showed that the abundance of methanotroph increased with the increasing O₂ concentrations. Type II methanotroph Methylocystis dominated in the enrichment cultures, accounting for 54.8, 48.1, and 36.9 % of the total bacterial 16S rRNA gene sequencing reads in HO, LO-1, and LO-2, respectively. Methylotrophs, mainly including Methylophilus, Methylovorus, Hyphomicrobium, and Methylobacillus, were also abundant in the cultures. Compared with the O₂ sufficient condition (21 %), higher microbial biodiversity (i.e., higher Simpson and lower Shannon indexes) was detected in LO-2 enriched at the initial O₂ concentration of 2.5 %. These findings indicated that compared with the O₂ sufficient condition, more CH₄-derived carbon was exuded into the environments and promoted the growth of non-methanotrophic microbes in O₂-limiting environments.

Particulate matter (PM) inhalation is an established trigger of cardiovascular events such as cardiac arrhythmias that occur within hours to days after exposure. Higher daily PM levels are related to acute increases in systemic arterial blood pressure (BP). The aim of the present study was to evaluate the effects of PM₁₀ on electrocardiogram (ECG) parameters, blood pressure, lipid peroxidation (MDA), xanthine oxidase, and antioxidant enzyme in healthy rats and also to examine the protective effects of vanillic acid (VA) in this respect. Eighty male Wistar rats were divided into eight groups (n = 10), namely control (normal saline, gavage), VAc (10 mg/kg), sham (normal saline, intratracheal instillation), VA (10 mg/kg VA, 10 days gavage +0.1 ml normal saline, intratracheal instillation), PM1 (0.5 mg/kg), PM2 (2.5 mg/kg), PM3 (5 mg/kg), PM3 + VA (5 mg/kg, intratracheal instillation + 10 mg/kg VA, 10 days, gavage) groups. The rats were anesthetized and 0.1 ml of saline as well as a certain concentration of PM₁₀ was instilled into the trachea and it was repeated after 48 h, then 30 min after that, PR interval, QTc, and systolic blood pressure were measured. The activities of antioxidant enzymes, xanthine oxidase (XOX), and malondialdehyde (MDA) were measured in plasma by special Kits. A significant increase in blood pressure (BP), PR interval, QTc, MDA, and XOX and a significant decrease in antioxidant enzyme (CAT, SOD, and GPx) occurred in PM₁₀ groups. Vanillic acid ameliorated blood pressure, QTc, PR interval, XOX, MDA, and increased antioxidant enzymes (SOD, CAT, and GPx) significantly. In the present study, it was shown that PM₁₀ had devastating effects on the heart and blood pressure, probably due to the increased oxidative stress in healthy rats. Vanillic acid could improve the symptoms of PM₁₀ exposure and can be used as an antioxidant agent against the harmful effects of PM₁₀.

Natural population of Bufo melanostictus in response to environmental cues shows several physiologic changes such as reproductive activity, hibernation, aestivation and metabolic depression in different seasons. We investigated the effects of seasonal fluctuations on oxidative stress (OS) physiology biomarkers, such as endogenous (ELPx) and induced (ILPx) lipid peroxidation, front-line redox regulatory enzymes (superoxide dismutase: SOD and catalase) and two non-enzyme antioxidant metabolites (ascorbic acid and reduced glutathione) in liver, gonad and cerebral hemisphere of toads collected from the Bhubaneswar area of India, where temperature fluctuates considerably rising to the highest in summer (∼46 °C) and being lowest in winter (<10 °C). Soil and air of the sampling site, although varying seasonally, were mostly found to be unpolluted, except for suspended particulate matter and respiratory particulate matter that were above recommended value. The magnitude of both ELPx and ILPx levels in most of the tissues, for example, ELPx in liver, cerebral hemisphere and ovary, and ILPx in liver of males and ovary, were found to be higher in rainy season in comparison to the other seasons. Nevertheless, levels of both ELPx and ILPx were low in testes in rainy season in comparison to the other two seasons. No correlation was observed between temperature and the studied OS parameters except a positive correlation with SOD and negative correlations with non-enzymatic small redox regulatory molecules in some selected tissues. Conversely, discriminant function analysis reveals a clear impact of the changing season on OS physiology of the toad. It implies that season considerably modulates OS physiology which be a reflection of the toads to abiotic pollutants alone and/or as results of metabolic changes under hibernation, aestivation and due to reproductive activities. Therefore, seasonal changes in OS physiological responses in poikilothermic models especially in toads must be cautiously used as indicators to assess environmental impact, mainly soil pollution. Results of the present study may be used as baseline data for any future analyses of the physiological impacts of environmental changes using toads as model organism.

Surfaces of fly ashes from three Swedish MSW incinerating plants were extensively characterized to better predict their involvement in the generation of persistent organic pollutants. The ashes were then subjected to thermal treatment at 400 °C in sealed glass ampoules to track the decomposition polychlorinated dibenzo-p-dioxins and furans (PCDD and PCDF). Temperature programmed desorption experiments in the 30–900 °C range also enabled monitoring of thermally decomposing ashes by Fourier Transform Infrared (FTIR) spectroscopy as well as thermally desorbing effluent gases by mass spectrometry. In addition, one ash was doped with ¹³C-labelled PCDD and PCDF to evaluate the potential of the experimental setup for elucidating the thermal desorption of the organic molecules. It was found that in ashes with high carbon content PCDD and PCDF decomposition were led pronounced, and that PCDD degraded more readily than PCDF.

Behaviors of BDE-28 and BDE-47 in two distinct soils (Phaeozem and Acrisol) as affected by the separate addition of root exudate components (i.e., oxalic acid, glycine, and fructose) were investigated by a soil microcosm incubation experiment. The results showed that root exudate components promoted the desorption of BDE-28 (57.6–235.0 %) and BDE-47 (56.9–223.7 %) from the soils due to the enhancement of their water solubilities. The addition of root exudate components increased the n-butanol extractability of BDE-28 and BDE-47 by 20.3–72.5 and 48.6–169.2 %, respectively, which had a positive correlation with the concentrations of dissolved organic carbon (DOC) in the soils (p < 0.01), suggesting that the increase of DOC in the soils by root exudate components was the major factor to enhance the extractability. Fructose and oxalic acid promoted the desorption and increased the availability of BDE-28 and BDE-47 in the soils more efficiently than glycine. The addition of different root exudate components resulted in distinct shifts in soil microbial community structure (p < 0.05). Oxalic acid caused the greatest impacts on the soil bacterial communities and increased the degradation rates of BDE-28 and BDE-47 most obviously. The findings of this study clarified the roles of root exudate components in affecting the behaviors of polybrominated diphenyl ethers (PBDEs) in soils.

Chamber studies were performed to investigate the efficiency of a photocatalytically active cementitious coating material to depollute contaminated air. The results showed a photocatalytic effect on ozone (O₃), proven by an increase of the geometric uptake coefficient from 5.2 × 10⁻⁶ for the inactive to 7.7 × 10⁻⁶ for the active material under irradiation. Measured first-order rate constants for nitrogen oxides (NOₓ) under irradiation are in the range of 2.6–5.9 × 10⁻⁴ s⁻¹, which is significantly higher compared to the inactive material (7.3–9.7 × 10⁻⁵ s⁻¹) demonstrating the photocatalytic effect. However, no significant photocatalytic degradation was observed for the studied volatile organic compounds (VOCs) toluene and isoprene resulting in only an upper limit uptake coefficient of 5.0 × 10⁻⁷ for both VOCs. In all experiments using the photocatalytically active material, a clear formation of small carbonyl (C1–C5) gas phase compounds was identified which is suggested to result from the photocatalytic degradation of organic additives. In contrast to the uptake observed for pure O₃, during the experiments with NOₓ (≥50 % relative humidity), a clear photocatalytic formation of O₃ was observed. For the material investigated, an empirically derived overall zero-order rate constant of k ₀ (O₃) ≈ 5 × 10⁷ molecules cm⁻³ s⁻¹ was determined. The results demonstrate the necessity of detailed studies of heterogeneous reactions on such surfaces under more complex simulated atmospheric conditions as enabled by simulation chambers.

The presented research concerned the compatibility of cosolvents with in situ alkaline hydrolysis (ISAH) for treatment of organophosphorous (OPP) pesticide contaminated sites. In addition, the influence of moderate temperature heat increments was studied as a possible enhancement method. A complex dense non-aqueous phase liquid (DNAPL) of primarily parathion (~50 %) and methyl parathion (~15 %) obtained from the Danish Groyne 42 site was used as a contaminant source, and ethanol and propan-2-ol (0, 25, and 50 v/v%) was used as cosolvents in tap water and 0.34 M NaOH. Both cosolvents showed OPP solubility enhancement at 50 v/v% cosolvent content, with slightly higher OPP concentrations reached with propan-2-ol. Data on hydrolysis products did not show a clear trend with respect to alkaline hydrolysis reactivity in the presence of cosolvents. Results indicated that the hydrolysis rate of methyl-parathion (MP3) decreased with addition of cosolvent, whereas the hydrolysis rate of ethyl-parathion (EP3) remained constant, and overall indications were that the hydrolysis reactions were limited by the rate of hydrolysis rather than NAPL dissolution. In addition to cosolvents, the influence of low-temperature heating on ISAH was studied. Increasing reaction temperature from 10 to 30 °C provided an average rate of hydrolysis enhancement by a factor of 1.4–4.8 dependent on the base of calculation. When combining 50 v/v% cosolvent addition and heating to 30 °C, EP3 solubility was significantly enhanced and results for O,O-diethyl-thiophosphoric acid (EP2 acid) showed a significant enhancement of hydrolysis as well. However, this could not be supported by para-nitrophenol (PNP) data indicating the instability of this product in the presence of cosolvent.

Acetaminophen (ACT) is one of the most frequently detected pharmaceuticals in aqueous environments, and treatment of ACT were generally carried out by photocatalytic degradations under high energy UV irradiation. In this study, potassium ferricyanide was utilized as a quadruple-elemental dopant in a TiO₂ photocatalyst in order to enhance its visible-light activity. Two critical parameters (amounts of dopants and durations of calcination) of the synthesis of the photocatalyst by a sol–gel method were systematically evaluated. Crystal structure of the doping TiO₂ was examined by X-ray diffraction while the effects of the two parameters on the photocatalytic activity were elucidated by various characterizations. Increasing the amount of dopant or the duration of calcination red-shifted the UV–vis DRS of the doped TiO₂. The estimated band gap energy of the doped TiO₂ decreased slightly as the amount of dopant increased, but it increased as the duration of calcination increased. The FT-IR yielded characteristic peaks that revealed the effects of the two parameters, whereas the SEM images revealed the morphological evolutions of each effect. The photocatalyst, synthesized at optimum conditions was able to remove 99.1 % acetaminophen with rate constant of 7.9 × 10⁻³ min⁻¹, which was 4.88 times greater than virgin TiO₂. In general, this study not only optimized synthetic conditions of the new visible-light active photocatalyst for ACT degradation but also presented characterizations conducted by SEM, XRD, UV–vis DRS, and FTIR to elucidate the relationship between modified structure and the photocatalytic activity. Graphical abstract Effects of doping amounts of K₃[Fe(CN)₆] and calcunation duration on visible light absorbance of TiO₂ photocatalysts

The present study elaborates the removal of endosulfan, an emerging water pollutant and potential carcinogenic, in aerated solution. The influence of Cl⁻, NO₃ ⁻, NO₂ ⁻, CO₃ ²⁻, HCO₃ ⁻, SO₃ ²⁻, and humic acid was assessed on the radiolytic degradation of endosulfan. A strong inhibition on the radiolytic degradation of endosulfan was observed in the presence of NO₃ ⁻, NO₂ ⁻, and SO₃ ²⁻. Instead, a slight increase in the removal efficiency of endosulfan was observed at high concentrations of CO₃ ²⁻ and HCO₃ ⁻. The formation of CO₃ •⁻ in radiolytic degradation of endosulfan in the presence of CO₃ ²⁻ and HCO₃ ⁻ was demonstrated by adding SO₃ ²⁻ that rapidly react with CO₃ •⁻. The results indicate that CO₃ •⁻ formed from the reactions of CO₃ ²⁻ and HCO₃ ⁻ and commonly found in natural water can play an important role in the degradation of endosulfan and other sulfur containing electron-rich compounds. The study showed faster degradation of endosulfan at lower concentration compared to high concentration and removal was found to follow pseudo-first-order kinetic. Endosulfan ether was found as the main degradation product and degradation pathway was found to be initiated at the S=O bond of endosulfan. The efficiency of gamma irradiation in the removal of endosulfan was examined in terms of formation of short chain organic acids and chloride ion accumulation.

The mixing layer theory is not suitable for predicting solute transfer from initially saturated soil to surface runoff water under controlled drainage conditions. By coupling the mixing layer theory model with the numerical model Hydrus-1D, a hybrid solute transfer model has been proposed to predict soil solute transfer from an initially saturated soil into surface water, under controlled drainage water conditions. The model can also consider the increasing ponding water conditions on soil surface before surface runoff. The data of solute concentration in surface runoff and drainage water from a sand experiment is used as the reference experiment. The parameters for the water flow and solute transfer model and mixing layer depth under controlled drainage water condition are identified. Based on these identified parameters, the model is applied to another initially saturated sand experiment with constant and time-increasing mixing layer depth after surface runoff, under the controlled drainage water condition with lower drainage height at the bottom. The simulation results agree well with the observed data. Study results suggest that the hybrid model can accurately simulate the solute transfer from initially saturated soil into surface runoff under controlled drainage water condition. And it has been found that the prediction with increasing mixing layer depth is better than that with the constant one in the experiment with lower drainage condition. Since lower drainage condition and deeper ponded water depth result in later runoff start time, more solute sources in the mixing layer are needed for the surface water, and larger change rate results in the increasing mixing layer depth.