The estimated diffusion fluxes of methane (CH₄) and carbon dioxide (CO₂) at the sediment–water interface in the Rzeszów Reservoir in southeastern Poland are presented. The relevant studies were conducted during 2009, 2010, and 2011. Calculated fluxes ranged from 0.01 to 2.19 mmol m⁻² day⁻¹and from 0.36 to 45.33 mmol m⁻² day⁻¹for methane and carbon dioxide, respectively. While the values for calculated diffusion fluxes of methane are comparable with those reported for other eutrophic reservoirs, much higher values were obtained here for carbon dioxide. The resulting values of δ¹³C-CH₄and the fractionation coefficients between methane and carbon dioxide (αCH₄-CO₂) suggest that methane in the sediment of the Rzeszów Reservoir is produced by acetate fermentation, while the hydrogenotrophic methanogenic process is of successively greater importance with increasing depth. In the top layer of the sediment, 24–72 % of CO₂came from methanogenesis, while the contribution made by the degradation of organic matter by methanogenesis to CO₂was greater in the deeper layer.

The behaviour of sulphate-reducing microbial community was investigated at the oxic–anoxic interface (0–2 cm) of marine sediments when submitted to oil and enhanced bioturbation activities by the addition of Hediste diversicolor. Although total hydrocarbon removal was not improved by the addition of H. diversicolor, terminal restriction fragment length polymorphism (T-RFLP) analyses based on dsrAB (dissimilatory sulphite reductase) genes and transcripts showed different patterns according to the presence of H. diversicolor which favoured the abundance of dsrB genes during the early stages of incubation. Complementary DNA (cDNA) dsrAB libraries revealed that in presence of H. diversicolor, most dsrAB sequences belonged to hydrocarbonoclastic Desulfobacteraceae, suggesting that sulphate-reducing microorganisms (SRMs) may play an active role in hydrocarbon biodegradation in sediments where the reworking activity is enhanced. Furthermore, the presence of dsrAB sequences related to sequences found associated to environments with high dinitrogen fixation activity suggested potential N₂ fixation by SRMs in bioturbated-polluted sediments.

Understanding the biogeochemistry of metal-contaminated peatlands is important for predicting the impact of mining and industrial activities on peatlands and downstream surface waters and for predicting recovery of previously impacted sites. The objective of this work was to characterize the factors controlling spatial and temporal variability in surface peat (0–15 cm) and pore water chemistry of 18 regionally representative peatlands in Sudbury, Ontario, Canada. The pollution gradient is clearly evident as Cu and Ni concentrations in surface peat are elevated close to the main Copper Cliff smelter. Surface peat also differs greatly in acidity (pH) and organic matter content among sites, and dissolved organic carbon (DOC) concentrations in pore water are positively correlated with peat carbon content. In addition, sites having surface peat that is more decomposed also have pore water DOC that is more humified. Pore water chemistry varies seasonally; samples taken in late summer and fall were characterized by higher SO₄, and lower pH and higher concentrations of base cations and metals such as Ni, Co, and Mn compared with those in late spring that had higher DOC, higher pH, and higher concentrations of metals such as Cu and Fe. Despite the large spatial and temporal variability in pore water chemistry, soil-solution partitioning (K d) of some metals (Ni, Co, and Mn) can be explained by pH alone. Modeling soil-solution partitioning for these metals and Cu, Al, and Fe is significantly improved with the addition of SO₄; dissolved organic matter quality and quantity and/or the δ¹⁸O signature of the pore water in regression models indicating several factors other than acidity has an influence on pore water chemistry.

A novel magnetic pyridinium-functionalized mesoporous silica adsorbent (Fe₃O₄@SiO₂@Py-Cl) was synthesized for nitrate removal from aqueous solutions. The adsorption performances were investigated by varying experimental conditions such as pH, contact time, and initial concentration. The adsorbent was characterized by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR) spectroscopy, and magnetic hysteresis loops. The results showed that the adsorption equilibrium could be reached within 30 min and the kinetic data were fitted well by pseudo-second-order and intra-particle diffusion model. The adsorbent exhibited a favorable performance, and its maximum adsorption capacity calculated by the Langmuir isotherm model was 1.755 mmol/g. The nitrate adsorption mechanism was mainly controlled by the material through ion exchange of nitrate with chloridion, as determined by XPS. This study indicated that this novel pyridinium-functionalized mesoporous material had excellent adsorption capacity. Meanwhile, compared with other adsorbents, it could remove nitrate fast and easy to be collected by magnetic separation, showing great potential application for nitrate removal from aqueous solution.

The biodegradation of organic compounds present in water at trace concentration has become a critical environmental problem. In particular, enzymatic oxidation by fungal laccases offers a promising alternative for efficient and sustainable removal of organic pollutants in water. In this work, the biocatalytic ability of laccases from the Pycnoporus sanguineus CS43 fungus was evaluated. A filtered culture supernatant (laccase cocktail) evidenced an enhanced biotransformation capability to remove common endocrine-disruptor compounds (EDCs), such as bisphenol A, 4-nonylphenol, 17-α-ethynylestradiol and triclosan. A biodegradation of around 89–100 % was achieved for all EDCs using synthetic samples (10 mg L⁻¹) and after the enzymatic treatment with 100 U L⁻¹ (50.3 U mg ⁻¹). The biodegradation rates obtained were fitted to a first order reaction. Furthermore, enzymatic biocatalytic activity was also evaluated in groundwater samples coming from northwestern Mexico, reaching biotransformation percentages between 55 and 93 % for all tested compounds. As far as we know this is the first study on real groundwater samples in which the enzymatic degradation of target EDCs by a laccase cocktail from any strain of Pycnoporus sanguineus was evaluated. In comparison with purified laccases, the use of cocktail offers operational advantages since additional purification steps can be avoided.

During the extraction of coal bed methane (CBM), entrapped in the deep layers of different coal beds, large amount of coal bed water (CBW) is also simultaneously released. The quality of this water is generally very poor which may often contaminate the adjoining soil environment adversely. In the present study, some major changes occurring in CBW-contaminated soils were assessed with relation to nearby non-affected soils. The CBW was found to be moderately saline and highly alkaline in nature with high sodium absorption ratio (SAR) values. Contamination with this water affected the soil environments substantially resulting in significantly increased pH and exchangeable sodium percentage (ESP) in the affected soils thus rendering the soils unsuitable for undertaking common agricultural practices. However, in spite of moderately high electrical conductivity values of this contaminating water, the resultant increments in salinity status of the soils were not observed to reach near the critical level. This behaviour was attributed to light texture of these soils which probably helped in leaching of a part of the soluble salts. Some microbial properties as well as availability of nitrogen and phosphorus were also found to decline in these CBW-affected soils. The study showed that utmost care needs to be exercised before release of CBW during extraction of CBM. In case of any contamination to nearby arable soils, suitable amendment practices for alkaline soils need to be adopted to mitigate the adverse effects of such water on soil environment.

Nitrogen inputs to coastal watersheds have been linked to eutrophication. However, the role that domestic sources of wastewater play in contributing nitrogen to coastal watersheds is not well known in the southeastern USA. In a yearlong study (2011–2012), nitrogen concentrations were compared in watersheds served by septic systems and a centralized sewer system in the Coastal Plain of North Carolina. Surface and groundwater samples from septic systems and sewer watersheds were analyzed for total dissolved nitrogen (TDN), total nitrogen, and nitrogen and oxygen isotopes in nitrate. Groundwater beneath the drainfield and adjacent to streams had median concentrations of TDN at 5.9 and 4.4 mg/L, respectively. Additionally, median groundwater-transported loads of TDN to the stream from septic systems sites (0.6 kg-TDN/year) were significantly greater than sites in sewer watersheds (0.2 kg-TDN/year). Isotopic analyses revealed that effluent from septic systems was the primary source of nitrate in watersheds served by septic systems, while fertilizer and/or soil organic matter were dominant sources of nitrate in sewer watersheds. Nitrogen exported from septic systems contributed to elevated nitrogen concentrations in groundwater and streams throughout the watershed, whereas nitrogen exports from sewers were focused at a single point source and affected surface water concentrations. Based on watershed TDN exports from septic systems minus TDN exports from sewers watersheds, it was estimated that septic systems contributed 1.6 kg TDN/ha/year to watershed exports of TDN. Overall, septic systems and sewers contributed to elevated nitrogen loading and should be considered in nutrient-sensitive watershed management.

Plant peroxidases have strong potential utility for decontamination of phenol-polluted wastewater. However, large-scale use of these enzymes for phenol depollution requires a source of cheap, abundant, and easily accessible peroxidase-containing material. In this study, we show that potato pulp, a waste product of the starch industry, contains large amounts of active peroxidases. We demonstrate that potato pulp may serve as a tool for peroxidase-based remediation of phenol pollution. The phenol removal efficiency of potato pulp was over 95 % for optimized phenol concentrations. The potato pulp enzymes maintained their activity at pH 4 to 8 and were stable over a wide temperature range. Phenol solutions treated with potato pulp showed a significant reduction in toxicity compared with untreated phenol solutions. Finally we determined that this method may be employed to remove phenol from industrial effluent with over 90 % removal efficiency under optimal conditions.

Acidic deposition is a worldwide problem that often leads to the increase in soil available heavy metals. Liming and biochar can both raise soil pH and immobilize heavy metals. An experiment was conducted in the laboratory to study the effects of acidic deposition on soil Cd mobility and soil biological activity in a soil polluted with Cd. Biochar, prepared from poultry litter biochar (PLB) or eucalyptus biochar (EB) was added at a rate of 3 %. Liming controls, bringing the soil to the same pH as that attained with biochar, were also used. The experimental results showed a higher risk of Cd leaching and impaired biological properties under simulated acid rain. Biochar addition resulted in a reduction in the risk of leaching and in improved biological properties and could provide benefits over liming for the management of soil polluted with heavy metals, especially in areas affected by acidic deposition.

The search for new bacterial consortia capable of removing PAH from the environment is associated with the need to employ novel, simple, and economically efficient detection methods. A fluorimetric method (FL) as well as high voltage electrochemiluminescence (ECL) on a modified surface of an aluminum electrode were used in order to determine the changes in the concentrations of PAH in the studied aqueous solutions. The ECL signal (the spectrum and emission intensity for a given wavelength) was determined with the use of an apparatus operating in single photon counting mode. The dependency of ECL and FL intensity on the concentration of naphthalene, phenanthrene, and pyrene was linear in the studied concentration range. The biodegradation kinetics of the particular PAH compounds was determined on the basis of the obtained spectroscopic determinations. It has been established that the half-life of naphthalene, phenanthrene, and pyrene at initial concentrations of 50 mg/l (beyond the solubility limit) reached 41, 75, and 130 h, accordingly. Additionally, the possibility of using ECL for rapid determination of the soluble fraction of PAH directly in the aqueous medium has been confirmed. Metagenomic analysis of the gene encoding 16S rRNA was conducted on the basis of V4 hypervariable region of the 16S rRNA gene and allowed to identify 198 species of bacteria that create the S4consortium. The consortium was dominated by Gammaproteobacteria (78.82 %), Flavobacteria (9.25 %), Betaproteobacteria (7.68 %), Sphingobacteria (3.76 %), Alphaproteobacteria (0.42 %), Clostridia (0.04 %), and Bacilli (0.03 %).