Although sulfonamides (SAs) are among the most commonly used veterinary drugs and their presence in the environment is well documented, knowledge of their fate and behavior in the soil environment is still limited, especially for sulfisoxazole (SSX) which is characterized by the lowest (among other SAs) pK ₐ value associated with acid-base equilibrium of sulfonamide group. Thus, this work was focused on determining the sorption potential of SSX onto natural soils differing in physicochemical properties. All the results were modeled using linear, Freundlich, Langmuir, Dubinin–Radushkevich, and Temkin sorption isotherms. The established sorption coefficients (K d) for SSX were quite low (from 0.27 to 0.95 L kg⁻¹), which indicated that this substance is highly mobile and has the potential to run off into surface waters and/or infiltrate ground water. The sorption data of SSX is well fitted to the Freundlich isotherm model (R ² > 0.968). Moreover, we assessed the sorption mechanism of these compounds in the edaphic environment with respect to organic matter (OM) content, pH, and ionic strength. To clarify the current state of knowledge, these factors were examined much more thoroughly than in previous investigations concerning other SAs. The wide range of ionic strength examined showed positive correlation of this factor and sorption of SAs. The results also yielded new insight into dependency of sorption of SAs on organic matter content in soil.

Atmospheric ozone-terpene reactions, which form secondary organic aerosol (SOA) particles, can affect indoor air quality when outdoor air mixes with indoor air during ventilation. This study, conducted in Leipzig, Germany, focused on limonene-induced particle formation in a genuine indoor environment (24 m³). Particle number, limonene and ozone concentrations were monitored during the whole experimental period. After manual ventilation for 30 min, during which indoor ozone levels reached up to 22.7 ppb, limonene was introduced into the room at concentrations of approximately 180 to 250 μg m⁻³. We observed strong particle formation and growth within a diameter range of 9 to 50 nm under real-room conditions. Larger particles with diameters above 100 nm were less affected by limonene introduction. The total particle number concentrations (TPNCs) after limonene introduction clearly exceed outdoor values by a factor of 4.5 to 41 reaching maximum concentrations of up to 267,000 particles cm⁻³. The formation strength was influenced by background particles, which attenuated the formation of new SOA with increasing concentration, and by ozone levels, an increase of which by 10 ppb will result in a six times higher TPNC. This study emphasizes indoor environments to be preferred locations for particle formation and growth after ventilation events. As a consequence, SOA formation can produce significantly higher amounts of particles than transported by ventilation into the indoor air.

In order to understand the sources and potential formation processes of atmospheric carbonaceous aerosols in South China, fine particle samples were collected at a high-elevation mountain site—Mount Lu (29°35′ N, 115°59′ E, 1165 m A.S.L.) during August–September, 2011. Eight carbonaceous fractions from particles were resolved following the IMPROVE thermal/optical reflectance protocol. During the observation campaign, the daily concentrations of PM₂.₅ at Mount Lu ranged from 7.69 to 116.39 μg/m³, with an average of 58.76 μg/m³. The observed average organic carbon (OC) and elemental carbon (EC) concentrations in PM₂.₅ were 3.78 and 1.28 μg/m³, respectively. Secondary organic carbon (SOC) concentration, estimated by EC-tracer method, was 2.07 μg/m³ on average, accounting for 45.0 % of the total OC. The enhancement of secondary organic aerosol (SOA) formation was observed during cloud/fog processing, and heterogeneous acid-catalyzed reactions may have contributed to SOA formation as well. Back trajectory analysis indicated that air masses were mainly sourced from southern China during observation period, and this air mass source was featured by highest values of OC and effective carbon ratio (ECR). Relation of carbonaceous species and principal component analysis indicated that multiple sources contributed to the carbonaceous aerosols at Mount Lu.

The present study, the synthesis of silver nanoparticles (AgNPs) at 90 °C temperature using an aqueous extract from Ficus talboti leaf and the antioxidant and antibacterial activities of the AgNPs obtained. The devised method is simple and cost-effective, and it produces spherical AgNPs of size 11.9 ± 2.3 nm. The synthesized AgNPs was characterized as UV–vis spectrum and obtain a peak at 438 nm. The phytochemical study result shows that the secondary metabolites such as alkaloids, saponins, phenolic compounds, tannin, flavonoids, phytosterol, and glycosides may be responsible for reducing as well as capping silver ions into AgNPs. Transmission electron microscopic (TEM) studies of the particles revealed a dominance of spherical particle AgNPs. The face centered cubic structure of the AgNPs was confirmed by X-ray diffraction (XRD) peaks at 111°, 200°, 220°, and 311°; SAED patterns confirms the plane of silver nanoparticle planes with clear circular spots on the selected area electron diffraction (SAED). Elemental analysis was done by energy dispersive X-ray analysis (EDX). In addition, this study evaluated the in vitro antioxidant and antibacterial properties of the biosynthesized AgNPs that were found to be significant.

Apart from the conventional polyethylene and the bio-based or mainly bio-based biodegradable in soil mulching films, polyethylene mulching films of controlled degradation in soil are already used in agriculture. The use of special pro-oxidants as additives is expected to accelerate the abiotic oxidation and the subsequent chain scission of the polymer under specific UV radiation or thermal degradation conditions, according to the literature. The role of pro-oxidants in the possible biodegradation of polyethylene has been theoretically supported through the use of controlled laboratory conditions. However, results obtained in real soil conditions, but also several laboratory test results, are not supporting these claims and the issue remains disputed. Mulching films made of linear low-density polyethylene (LLDPE) with pro-oxidants, after being used for one cultivation period in an experimental field with watermelon cultivation, were buried in the soil under real field conditions. This work presents the analysis of the degradation of the mulching films during the cultivation period as compared to the corresponding changes after a long soil burial period of 8.5 years. The combined effects of critical factors on the photochemical degradation of the degradable mulching LLDPE films with pro-oxidants under the cultivation conditions and their subsequent further degradation behaviour in the soil are analysed by testing their mechanical properties and through spectroscopic and thermal analysis.

Bioaccumulation of Cd²⁺in soil bacteria might represent an important route of metal transfer to associated mycorrhizal fungi and plants and may have potential as a tool to accelerate Cd²⁺extraction in the bioremediation of contaminated soils. The present study examined the bioaccumulation of Cd²⁺in 15 bacterial strains representing three phyla (Firmicutes, Proteobacteria, and Bacteroidetes) that were isolated from the rhizosphere, ectomycorrhizae, and fruitbody of ectomycorrhizal fungi. The strains Pseudomonas sp. IV-111-14, Variovorax sp. ML3-12, and Luteibacter sp. II-116-7 displayed the highest biomass productivity at the highest tested Cd²⁺concentration (2 mM). Microscopic analysis of the cellular Cd distribution revealed intracellular accumulation by strains Massilia sp. III–116-18, Pseudomonas sp. IV-111-14, and Bacillus sp. ML1-2. The quantities of Cd measured in the interior of the cells ranged from 0.87 to 1.31 weight % Cd. Strains originating from the rhizosphere exhibited higher Cd²⁺accumulation efficiencies than strains from ectomycorrhizal roots or fruitbodies. The high Cd tolerances of Pseudomonas sp. IV-111-16 and Bacillus sp. ML1-2 were attributed to the binding of Cd²⁺as cadmium phosphate. Furthermore, silicate binding of Cd²⁺by Bacillus sp. ML1-2 was observed. The tolerance of Massilia sp. III-116-18 to Cd stress was attributed to a simultaneous increase in K⁺uptake in the presence of Cd²⁺ions. We conclude that highly Cd-tolerant and Cd-accumulating bacterial strains from the genera Massilia sp., Pseudomonas sp., and Bacillus sp. might offer a suitable tool to improve the bioremediation efficiency of contaminated soils.

This study investigated the microbial diversity established in a combined system composed of a continuous stirred tank reactor (CSTR), expanded granular sludge bed (EGSB) reactor, and sequencing batch reactor (SBR) for treatment of cellulosic ethanol production wastewater. Excellent wastewater treatment performance was obtained in the combined system, which showed a high chemical oxygen demand removal efficiency of 95.8 % and completely eliminated most complex organics revealed by gas chromatography–mass spectrometry (GC–MS). Denaturing gradient gel electrophoresis (DGGE) analysis revealed differences in the microbial community structures of the three reactors. Further identification of the microbial populations suggested that the presence of Lactobacillus and Prevotella in CSTR played an active role in the production of volatile fatty acids (VFAs). The most diverse microorganisms with analogous distribution patterns of different layers were observed in the EGSB reactor, and bacteria affiliated with Firmicutes, Synergistetes, and Thermotogae were associated with production of acetate and carbon dioxide/hydrogen, while all acetoclastic methanogens identified belonged to Methanosaetaceae. Overall, microorganisms associated with the ability to degrade cellulose, hemicellulose, and other biomass-derived organic carbons were observed in the combined system. The results presented herein will facilitate the development of an improved cellulosic ethanol production wastewater treatment system.

Activity concentration of ²³⁸U, ²³⁴U, ²²⁶Ra, ²²⁸Ra, ²¹⁰Pb and ²¹⁰Po in tap water from selected springs and private wells in the area of the former uranium mine at Žirovski Vrh were determined. A total of 22 tap water samples were collected at consumer’s houses. The results show that the activity concentrations of uranium in water samples are in range (0.17–372) and (0.22–362) mBq L⁻¹ for ²³⁸U and ²³⁴U, respectively. Radium activity concentrations are in range (0.14–16.7) and (0.9–11.7) mBq L⁻¹ for ²²⁶Ra and ²²⁸Ra, respectively. ²¹⁰Po activity concentration is in range (0.28–8.0) mBq L⁻¹ and can be regarded as the lowest amongst all analysed radionuclides. The range for ²¹⁰Pb is (0.5–24.6) mBq L⁻¹. Based on the results obtained for activity concentrations of six radionuclides, the committed effective dose for three different age groups of population were estimated. It was found that the committed effective dose was well below the recommended value of 100 μSv year⁻¹, ranging from 2.3 to 34.3 μSv year⁻¹ for adults, from 3.5 to 32.0 μSv year⁻¹ for children (7–12 years) and from 3.0 to 23.3 μSv year⁻¹ for infants.

Bioremediation has emerged as an environmental friendly strategy to deal with environmental pollution. Since the majority of polluted sites contain complex mixtures of inorganic and organic pollutants, it is important to find bacterial strains that can cope with multiple contaminants. In this work, a bacterial strain isolated from tannery sediments was identified as Acinetobacter guillouiae SFC 500-1A. This strain was able to simultaneously remove high phenol and Cr(VI) concentrations, and the mechanisms involved in such process were evaluated. The phenol biodegradation was catalized by a phenol-induced catechol 1,2-dioxygenase through an ortho-cleavage pathway. Also, NADH-dependent chromate reductase activity was measured in the cytosolic fraction. The ability of this strain to reduce Cr(VI) to Cr(III) was corroborated by detection of Cr(III) in cellular biomass after the removal process. While phenol did not affect significantly the chromate reductase activity, Cr(VI) was a major disruptor of catechol dioxygenase activity. Nevertheless, this activity was high even in presence of high Cr(VI) concentrations. Our results suggest the potential application of A. guillouiae SFC 500-1A for wastewaters treatment, and the obtained data provide the insights into the removal mechanisms, dynamics, and possible limitations of the bioremediation.

The aim of this study was to investigate (i) the behavior of native PBDEs during UV irradiation in different media, (ii) the possibility of their transformation into hydroxylated PBDEs in aqueous media, and (iii) the photochemistry/levels of brominated dioxins/furans formed from hydroxylated PBDEs. Debromination leading to the formation of a wide range of low-brominated congeners was the main path of photocatalyzed transformations of PBDEs. In organic solvents other than toluene, BDEs degraded in line with the pseudo first order kinetics (10–20 min half-life, depending on congener type and reaction medium). Irradiated BDE 209 congener behaved quite differently than lower-brominated BDEs: detectable amounts of various bromo-benzenes were found. That suggests that UV irradiation of BDE 209 leads to cleavage of the ether bound between the congener’s aromatic rings. Formation of bromophenyl bromo-methyl-biphenyl ethers or benzyl-bromophenoxybenzenes was observed in irradiated PBDE toluene-based solutions. The total concentration of OH-BDEs found in the reaction medium did not exceed 0.2 % of the initial precursor mass. Moreover, lower-brominated congeners detected in the reaction medium indicate subsequent debromination of OH-BDEs or hydro-debromination of the degraded congeners. Brominated dioxins and low levels of furans were observed in samples containing OH-BDEs. The total mass of dioxins did not exceed 3.5 % of the initial precursor mass.