The aim of this study was to develop a new experimental setup to determine parallel the emissions of greenhouse gases (GHG) and volatile organic compounds (VOCs) from silage during the opening as well as the subsequent aerobic storage phase of the complete bale without wrapping film. For this purpose, a special silage respiration chamber was used in which a silage bale could be examined. The gas analysis (CO₂, methanol, ethanol, ethyl acetate) of inlet, ambient and outlet air of the silage respiration chamber was carried out by photoacoustic spectroscopy. The gas samples taken inside the bale were analysed by gas chromatography for CO₂, O₂, CH₄, and N₂O. Three silage bales (grass and lucerne) as the smallest silage unit commonly used in practice were examined. The emission behaviour of the bales was recorded during experimental periods up to 55 days. The results allow a differentiation of the outgassing processes. On the one hand, gases produced during the anaerobic ensiling process (CO₂, CH₄, N₂O) are released once in a large amount during the first experimental hours after opening the silage. On the other hand, a continuous outgassing process takes place, which is particularly true for the VOCs ethanol, methanol, and ethyl acetate, whereby VOC emissions increase with rising ambient air temperatures. In this study, the emissions during the first 600 experimental hours from the grass silage bale and lucerne silage bale were 2313 g and 2612 g CO₂, 17.6 g and 145.2 g methanol, 132.3 g and 675.9 g ethanol, 55.1 g and 66.2 g ethyl acetate, respectively. Nevertheless, the focus of this study was on the technical recording of gas concentrations inside the silage bale itself and the emissions in the ambient air of the bale. For a better interpretation of the data, additional factors should be considered in further investigations.

The hydro-acoustic noise radiating from underwater tunnels during vehicle passage may be harmful to aquatic fauna, and this is a particular concern for endangered species. Therefore, the effects of underwater noise radiation and propagation on aquatic biodiversity must be investigated. In this study, the dynamic response of the sediment and tunnel structure in the Yangtze River in China was explored by conducting a field test, and the associated noise radiation from the tunnel was recorded and investigated. A three-dimensional numerical model was then developed to simulate the vibration of the tunnel-sediment coupling system induced by random traffic-flow models. Next, a modal acoustic transfer vector-based method was used to predict underwater noise radiation by use of a three-dimensional finite-element acoustic model. Finally, the accuracy of the simulated results was verified by comparison with measurements. The results showed that the noise radiation induced by passing vehicles was approximately 14 dB greater than the background noise, with a main frequency range of 12–25 Hz. The random traffic-flow model had obvious influence of the simulated noise level above 20 Hz. Vehicle-induced underwater noise may thus have a direct effect on fish species that can perceive low-frequency sound pressure. The proposed method can be used for further investigation of methods to reduce the effect of underwater noise on aquatic fauna, especially endangered species.

Estimates of the brown carbon (BrC) absorption and their contribution to light absorption in ambient aerosols are poorly understood. The existing approaches to apportion light absorption into black carbon (BC) and BrC mainly use the assumption of fixed angstrom absorption exponent (AAE) for BC (1.0), which is not always true for ambient aerosols. Besides, these estimates are seldom validated, leaving significant uncertainty with derived values. Also, BrC absorption studies are largely focused on aqueous extracts, which truly do not represent the aerosolized form, hence the relationship between aqueous extracts and aerosolized form is a subject of research. With this in mind, we collected ambient PM₂.₅ filter samples at Lumbini, Nepal, at the northern edge of the Indo-Gangetic Plains (IGP) during winter 2017-18. These samples were analyzed for different compositions of carbonaceous aerosol and optical properties. BC and BrC absorptions were derived using a preexisting simplified two-component model but with “improved conditions”. Although BC dominated spectral absorption, BrC contribution for the carbonaceous aerosol absorption increased substantially at ultraviolet wavelengths (example 14.8–53.6% at 365 nm). Further water-soluble BrC absorption value in aerosol was found to be higher by 1.8 times to that obtained in aqueous extracts. Water-soluble OC contributed ∼65% to OC loading and 50% to BrC absorption at 365 nm, indicated the equally important role of water-insoluble organics. Mass absorption efficiency (MAE) of water-soluble BrC in aerosol was found to be 1.7 m²/g, lower to water-insoluble by 2.2 times. High BC MAE was observed which showed positive dependence on secondary coating. Sample collected during events with fog droplets showed a reduction in carbonaceous components loading and light absorption but enhancement in MAE for BrC and BC, signifying that aqueous processing can significantly modify the aerosol optical properties.

Nano-magnetite supported by biochar (nFe₃O₄/BC) pyrolyzed at temperatures of 300 °C–600 °C was developed to activate hydrogen peroxide (H₂O₂) for the efficient degradation of ethylbenzene in aqueous solution. It was revealed that the degradation efficiency of ethylbenzene and TOC removal were 96.9% and 36.2% respectively after the reaction for 40 min in the presence of initial concentration of 0.1 mmol L⁻¹ ethylbenzene, 2.76 g L⁻¹ nFe₃O₄/BC₅₀₀ with the mass ratio of nFe₃O₄ to BC₅₀₀ of 4:1 and 2.0 mmol L⁻¹ H₂O₂ at pH 7.0. Based on electron paramagnetic resonance (EPR), quenching experiment and X-ray photoelectron spectroscopy (XPS) data, both OH and O₂⁻ radicals were generated in the nFe₃O₄/BC₅₀₀ activated H₂O₂ system, and the OH radicals were the predominant species for the degradation of ethylbenzene. Through electron transfer process, mechanisms of Fe(II), phenolic hydroxyl group and persistent free radicals (PFRs) on BC surfaces accounted for the generation of OH radicals, and Fe(III) in nFe₃O₄ and formed from Fe(II) oxidation responsible for the generation of O₂⁻ radicals in the nFe₃O₄/BC activated H₂O₂ system were proposed.

The effect of microplastics (MP) exposure on the chironomid species Chironomus riparius Meigen, 1804 was investigated using the OECD sediment and water toxicity test. Chironomid larvae were exposed to an environmentally relevant low microplastics concentration (LC), a high microplastics concentration (HC) and a control (C). The LC was 0.007 g m⁻² on the water surface + 2 g m⁻³ in the water column + 8 g m⁻² in the sediment, and the HC was 10 X higher than this for each exposure. The size of the majority of the manufactured microplastic pellets varied between 20 and 100 μm. The MP mixture consisted of: polyethylene-terephtalate (PET), polystyrene (PS), polyvinyl-chloride (PVC) and polyamide (PA) in a ratio of 45%: 15%: 20%: 20%, respectively, for the sediment exposure; 100% polyethylene for the water column exposure; and 50% polyethylene: 50% polypropylene for the water surface exposure. Different endpoints were monitored, including morphological changes in the mandibles and mentums of 4th instar larvae, morphological changes in the wings, mortality, emergence ratio, and developmental time. A geometric morphometric analysis showed a tendency toward widening of the wings, elongation of the mentums and changing the shape of the mandibles in specimens exposed to both concentrations of microplastics. The development time of C. riparius was significantly prolonged by the MP treatment: 13.8 ± 0.5; 14.4 ± 0.6; and 15.3 ± 0.4 days (mean ± SD) in the C, LC, and HC, respectively. This study indicates that even environmentally relevant concentrations of MP mixture have a negative influence on C. riparius, especially at the larval stage.

Fine particulate matter (PM₂.₅) pollution has become a worldwide environmental concern because of its adverse impacts on human health. This study aimed to explore the spatiotemporal variations and influencing factors of PM₂.₅ concentrations in Beijing during the 2013–2018 period, and further analyzed the impacts of environmental protection policies implemented in recent years. Notably, this study employed various statistical methods, i.e., ordinary Kriging interpolation, spatial autocorrelation analysis, time-series analysis and the Bonferroni test, to evaluate the regional and seasonal differences of PM₂.₅ concentrations based on long-term monitoring data. The results illustrated that PM₂.₅ concentrations decreased on a yearly basis, demonstrating that air pollution control policies have achieved initial success. Furthermore, PM₂.₅ concentrations were higher in the winter and in the southern regions. Diurnal variation presented a bimodal distribution, which varied slightly with the season. Relative humidity and wind speed were the principal meteorological factors affecting the distribution of PM₂.₅ concentrations, while precipitation had essentially no effect. A high positive correlation between PM₂.₅ and gaseous pollutants (SO₂, NO₂, and CO) indirectly reflected the contribution of automobile exhaust and coal-fired emissions. Generally, PM₂.₅ concentrations demonstrated strong spatiotemporal variations, and meteorological factors and pollutant emissions played an important role in this.

Nano-silica as an important part of soil is an ideal carrier of passivator material. In this paper, nano-silica was modified by silane coupling agent containing mercapto group and iron (II) salt to afford an organic-inorganic hybrid containing –S-Fe-S functional group (coded as RNS-SFe) on the surface of nano-silica. Results demonstrate that the RNS-SFe nanoparticle has network-like spheroidal shape and a primary particle size is about 18.0 nm. The RNS-SFe hybrid as a potential immobilization agent for heavy metal in soil shows excellent performance for the remediation of the contaminated soil. Specifically, with a dosage of 3.0% (mass ratio) in the soil, it can immobilize bioavailable Pb, Cd, and As by 97.1%, 85.0%, and 80.1%, respectively. Namely, the RNS-SFe hybrid can transform the bioavailable Pb, Cd, and As into insoluble mercapto metal compounds (–S-Pb-S- and –S-Cd-S-) and less soluble iron arsenate (Fe₃(AsO₄)₂, FeAsO₄) precipitate on the surface of nano-silica particle, thereby reducing the toxicity and mobility of the toxic contaminant fractions. In the meantime, the immobilized products of the Pb, Cd and As fractions have good resistance against acid leaching. These results are contributive to the application of RNS-SFe for the remediation of multi-heavy metal-contaminated soils in field.

The objectives of this research are: identify the hydrocarbons in water from the Bitzal River, Tabasco; select a carbon source that serves as a representative substrate of the determined compounds; and finally, design an experimental proposal for bioreactors that are capable of consuming compounds formed by complex mixtures and, therefore be effective in the elimination of specific hydrocarbons. We identified 16 compounds that belong to different hydrocarbon fractions. Pentacene (24.3 ± 0.09 mg L⁻¹), n-nonane (2.11 ± 0.96 mg L⁻¹) and benzo [a] pyrene (1.39 ± 0.57 mg L⁻¹) were the compounds with the highest concentrations in water. Two culture media, mineral medium and seawater were used. Diesel and Mayan crude oil were used for each culture medium, with a total of four bioreactors. Diesel represented light- and medium-fraction hydrocarbons, while Mayan crude oil represented the heavy fraction as well as the recalcitrant and polycyclic aromatic hydrocarbons (PAH). The maximum growth of suspended solids for diesel in mineral medium reached 2.95 g L⁻¹, and diesel was completely consumed in 8 days. In seawater, suspended solids for diesel reached 2.70 g L⁻¹, and diesel was consumed in 12 days. For Mayan crude oil in mineral medium, suspended solids increased from 0.8 to 2.41 g L⁻¹, and Mayan crude oil was completely consumed in 12 days. Using seawater, Mayan crude oil also degraded in 12 days, and suspended solids growth reached 2.11 g L⁻¹. Compounds that simulate complex mixtures of hydrocarbons from light to heavy fractions could be degraded, and the use of bioreactors is an alternative method of hydrocarbon pollution remediation in the Bitzal River.

Organ carbon are often used to enhance denitrification in wastewater treatment. However, their possible effects on microbial interactions are very limited. In this work, an anaerobic ammonium oxidation (anammox) coupled with sulfur autotrophic/mixotrophic denitrification (SAD/SMD) system was used to investigate the changes in microbial interactions among the microbial communities under different nutrient condition. The removal efficiency of total nitrogen increased from 70% (SAD) to 97% (SMD). The Illumina sequencing analysis indicated that Planctomycetes was the most dominant bacterial phylum in anammox system. Thiobacillus and Sulfurimonas, two typical autotrophic denitrifiers, decreased significantly from 31.9% to 17.7%–12.2% and 9.3%, when the nutrient condition changed from SAD to SMD (P < 0.05). Meanwhile, some heterotrophic or mixotrophic denitrifying bacteria, including Gemmobacter, Pseudomonas and Thauera increased significantly (P < 0.05). Molecular ecological network (MEN) analysis showed that the addition of organic carbon substantially altered the overall architecture of the network. Compared with SAD, the SMD had shorter path lengths, indicating higher transfer efficiencies of information and materials among different microorganism. The addition of organic carbon increased the microbial interaction complexity of Proteobacteria. The links of Thiobacillus, which was a typical sulfur-oxidizing autotrophic denitrifying bacteria, significantly reduced (P < 0.05) with the addition of organic carbon, while the links of the heterotrophic bacteria Geobacter significantly increased (P < 0.05). This study provided new insights into our understanding of the shifts in the bacteria community and their microbial interactions under different nutrient conditions (SAD and SMD) in sulfur-supported denitrification system.

Microplastic debris is ubiquitous and yet sampling, classifying and enumerating this prolific pollutant in marine waters has proven challenging. Typically, waterborne microplastic sampling is undertaken using nets with a 333 μm mesh, which cannot account for smaller debris. In this study, we provide an estimate of the extent to which microplastic concentrations are underestimated with traditional sampling. Our efforts focus on coastal waters, where microplastics are predicted to have the greatest influence on marine life, on both sides of the North Atlantic Ocean. Microplastic debris was collected via surface trawls using 100, 333 and 500 μm nets. Our findings show that sampling using nets with a 100 μm mesh resulted in the collection of 2.5-fold and 10-fold greater microplastic concentrations compared with using 333 and 500 μm meshes respectively (P < 0.01). Based on the relationship between microplastic concentrations identified and extrapolation of our data using a power law, we estimate that microplastic concentrations could exceed 3700 microplastics m⁻³ if a net with a 1 μm mesh size is used. We further identified that use of finer nets resulted in the collection of significantly thinner and shorter microplastic fibres (P < 0.05). These results elucidate that estimates of marine microplastic concentrations could currently be underestimated.