Zobrazení zdroje stránky Eskesenrobb0181

Geochemical processes of sulfur (S) in river aquatic systems play a crucial role in environmental evolution. In this study, the distributions and sources of reduced inorganic sulfur (RIS) and organic sulfur (OS) in coastal river surface sediments were investigated. The results indicated that OS dominated total S (80%), and OS (i.e., humic acid sulfur, HAS; fulvic acid sulfur, FAS) correlated with the availability of labile organic matter (OM) and reactive iron (Fe). Terrigenous inputs and sulfurization contributed to the enrichment of FAS through the S reduction. Autochthonous biological inputs were potential sources of HAS from S oxidization. The X-ray photoelectron spectroscopy showed that the main sources of S in surface sediments were deposited as the form of organic ester-sulfate. Aquatic life could break S down further, producing reduced S compounds accumulated as thiols and RIS in anoxic sediments. RIS was dominated by acid volatile sulfur (AVS) and chromium (II)-reducible sulfur (CRS). Reactive Fe oxides were major control factors for the conversation from hydrogen sulfide (H2S) to AVS, whereas elemental sulfide (ES) controlled the conversion from AVS into CRS in coastal rivers.Identifying major adverse effects on aquatic organisms in environmental samples is still challenging, and metabolomic approaches have been utilized as non-target screening techniques in the context of ecotoxicology. While existing methods have focused on statistical tests or univariate analysis, there is the need to further explore a multivariate analytical method that captures synergetic effects and associations among metabolites and toxicants. Here we show a new tool for screening sediment toxicity in the environment. First, we constructed predictive models using the metabolomic profiles and the result of exposure tests, to discriminate the toxic effects of target substances. The developed models were then applied to sediment samples collected from an actual urban area that contain chromium, nickel, copper, zinc, cadmium, fluoranthene, nicotine, and osmotic stress, incorporated with exposure tests of the benthic amphipod Grandidierella japonica. As a result, the fitted models showed high predictive power (Q2 &gt; 0.71) and could detect toxicants from mixed chemical samples across a wide range of concentrations in test datasets. The application of the constructed models to river sediment and road dust samples indicated that almost all target substances were less toxic compared with the effects at LC50 levels. Only zinc showed slight increasing trends among samples, suggesting that the proposed method can be used for prioritization of toxicants. The present work made a direct connection between chemical exposures and metabolomic responses, and draws attention to the need for further studies on interactive mechanisms of metabolites in toxicological assessments.Ciprofloxacin is the most commonly prescribed antibiotic, and its widespread use poses threat to environmental safety. The removal of ciprofloxacin from contaminated water has remained a major challenge. The present study investigated adding nanoscale zero-valent iron (NZVI) and activated carbon (AC) on high-level ciprofloxacin removal in hydrolysis-acidogenesis stage of anaerobic digestion. The results showed that the degradation rate of ciprofloxacin increased from 22.61% (Blank group) to 72.41% after adding NZVI/AC with concentration of ciprofloxacin in effluent decreasing from 8.25 mg L-1 to 3.48 mg L-1. The volatile fatty acids (VFAs) yield increased by 173.7% compared with the Blank group. In addition, the NZVI/AC group achieved the highest chemical oxygen demand (COD) removal rate and acidogenesis rate. The microbial community analysis presented that hydrolytic and acidogenic bacteria and microorganisms related to degrading ciprofloxacin were obviously improved in the NZVI/AC group. Moreover, eleven transformation products and the main degradation pathways were proposed based on mass spectrometry information. In summary, the NZVI/AC addition supplied promising approach for ciprofloxacin wastewater treatment.The increased contamination of surface water with plastic waste is proportional to the increased consumption of products that use them as raw material. However, the impact of these residues on aquatic biota remains limited, mainly when it comes to nanoplastics (NPs). Thus, the aim of the current study is to test the hypothesis that the exposure of Ctenopharyngodon idella juveniles to polystyrene nanoplastics (PS NPs) at low concentrations (0.04 ng/L, 34 ng/L and 34 μg/L), for 20 days, leads to DNA damage and has mutagenic and cytotoxic effects on their erythrocytes. Comet assay enabled observing that DNA damage (inferred from the greater tail length, DNA percentage in the tail and Olive tail moment) induced by PS NPs has increased as the pollutant concentrations have increased, as well as that the formation of micronuclei and other nuclear abnormalities was equitable in animals exposed to this pollutant. On the other hand, there were significant changes in erythrocyte shape and size, oxidative stress generation (NO levels, lipid peroxidation, hydrogen peroxide), antioxidant system inhibition (mediated by total hepatic glutathione) and PS NPs accumulation in the liver and brain of animals exposed to higher concentrations of it. Therefore, the current study has confirmed the initial hypothesis and enhanced the knowledge about the genotoxic, mutagenic and cytotoxic potential of PS NPs in freshwater fish at early developmental stage, relating these effects to biochemical changes and significant accumulation of these nanomaterials. Besides, it is a warning about the (eco) toxicological risk represented by these nanopollutants in aquatic environments. CAPSULE Polystyrene nanoplastics are capable of inducing DNA damage, mutagenic and cytotoxicity changes in fish.Increasing amounts of plastic waste in the environment and their fragmentation into smaller particles known as microplastics (particles, less then 5mm) have raised global concerns due to their persistency in the environment and their potential to act as vectors for harmful substances or pathogenic microorganisms. One possible solution to this problem is biodegradation of plastics by microorganisms. However, the scientific information on plastic-degrading microorganisms is scattered across different scientific publications. We conducted a systematic literature review (SLR) with predefined criteria using the online databases of Scopus and Web of Science to find papers on bacterial biodegradation of synthetic petroleum-based polymers. The aims of this SLR were to provide an updated list of all of the currently known bacteria claimed to biodegrade synthetic plastics, to determine and define the best methods to assess biodegradation, to critically evaluate the existing studies, and to propose directions for futurotocols and include all essential information needed for repetition of the experiments by other research groups.Large river basins transport considerable nutrients to the ocean every year. However, phosphorus (P) generated by human activities not only threatens aquatic ecosystem health in the river basin, but also has a negative effect on the estuary water environment. To better understand the environmental effects of anthropogenic P in a mega basin, we examined its inputs and distribution characteristics, and analyzed the factors driving it in the Yangtze River Basin (YRB) and sub-catchments. Anthropogenic P flux in the sub-catchments gradually increased from upper to lower reaches, and hotspots were primarily concentrated in traditional agricultural areas such as the Sichuan Basin and the Middle-Lower Yangtze plains. Agricultural sources were the main anthropogenic P inputs, of which fertilizer P was the leading contributor and driver of P changes, but livestock manure also accounted for a high proportion. Presently, anthropogenic P inputs in the YRB are considerably higher than in other parts of the world. Although long-distance transportation allows some P from the entire basin to be deposited in freshwater, a large amount of P still reaches the estuary and has a negative effect on water quality, outweighing the influence of local coastal inputs. To maintain the ecological health of the river basin and estuary, it will be necessary to further improve P utilization efficiency and encourage greater cooperation between different regions in the river basin.The present study compared the effects of adding shrimp shell powder (SSP) at four levels comprising 0% (CK), 5% (L), 10% (M), and 15% (H) on the abundance of antibiotic resistance genes (ARGs) and the bacterial community succession during swine manure composting. The relative abundances of 5/11 ARGs were reduced in CK, and 7/11 in H. Moreover, the removal rate was enhanced by adding SSP. Thus, H decreased the total abundance of ARGs by 32.68%, whereas CK increased it by 6.31%. Redundancy analysis indicated that mobile genetic elements (MGEs) (46.6%) and the bacterial community (31.1%) mainly explained the changes in ARGs. H enhanced the removal of MGEs, prolonged the thermophilic phase, stabilized copper and zinc, and retained nitrogen. LEfSe analysis and non-metric multidimensional scaling indicated that the bacterial community changed in the composting process, and it was optimized by H. The abundances of the potential bacterial co-hosts (such as Lactobacillus, Corynebacterium_1, and Ornithinicoccus) of ARGs and MGEs were lower and the decomposition of organic matter was higher in H compared with CK. Thus, composting with 15% SSP can reduce the risk of ARGs and improve the practical value for agronomic application.Ammonia (NH3) volatilization in rice paddies may be affected by elevated atmospheric CO2 concentration ([CO2]) and temperature due to changes in plant and soil nitrogen (N) metabolism. At present, little is known about the individual and combined effects of CO2 enrichment and warming on NH3 volatilization under field conditions. An experiment was conducted in a rice paddy in Central China, after 4 years of warming and CO2 enrichment using open-top chamber (OTC) devices. Compared with ambient conditions, elevated [CO2] had no significant effects on NH3 volatilization, although increases in soil pH and urease activity were observed. The stimulation on plant N assimilation under CO2 enrichment might offset the possible enhancement on NH3 volatilization, as more soil N was absorbed by plant thus reducing NH3 loss potential. Elevated temperature increased NH3 volatilization significantly, which could be attributed to increased soil ammonium nitrogen (NH4+-N) concentration, pH, and urease activity. Combination of CO2 enrichment and warming caused the highest cumulative NH3 loss, which increased by 26.5% compared with ambient conditions, but the interaction was not significant. [https://www.selleckchem.com/products/nazartinib-egf816-nvs-816.html EGF816] Higher plant N uptake, soil NH4+-N concentration, pH and urease activity were also observed with co-elevation of [CO2] and temperature, but the combined effects were variable and not synergistic. Our findings confirm that field warming and CO2 enrichment cause more NH3 volatilization in rice paddies, among which warming effects are dominant, and suggest that improved N management or field practices are required to reduce NH3 losses under future climate change.