Krebsrhodes1891

More importantly, NET exposure induced the expressions of the genes (esr1, vtg1, hsd17b3, hsd11b2, ar) that are closely related to the steroid hormone pathways in the embryos/larvae stages, implying a precocious effects of NET in zebrafish. This study demonstrates that NET alters the expression of HPA- and HPG-axes related genes in zebrafish at early stages, pointing to the need for the same type of analysis during the zebrafish gonadal differentiation window.Previous studies have shown that the toxicity of graphene nanomaterials (GNMs) to bacteria are related to the surface functionalization, however, the involved mechanisms are not fully understood. The present study aims to explore the toxic mechanisms of differentially functionalized GNMs to bacteria from the aspects of physical interaction, oxidative damage and cell autolysis. Three basic functionalization of GNMs including carboxylation (G-COOH), hydroxylation (G-OH) and amination (G-NH2) were studied. G-COOH (66% viability vs CT group) and G-OH (54%) graphene showed higher toxicity to E. coli than G-NH2 (96%) within 3 h at a concentration of 50 mg/L. The three materials showed distinct physical interaction modes with bacterial cells. G-COOH and G-OH contact with cell membrane via their sharp edges thus causing more damage than G-NH2 which covered the bacteria attaching along the basal plane. The three GNMs showed similar radical generation capacities, thus the direct generation of radicals is not the mechanism causing the toxicity. Instead, the GNMs can oxidize the cellular antioxidant glutathione (GSH) thereby causing oxidative damage. The oxidative capacity follows the order G-COOH > G-OH > G-NH2, which correlated with the antibacterial activity. Cell autolysis, the degradation of cell wall component peptidoglycan, was found to be a new mechanism inducing the death of bacteria. G-COOH and G-OH caused more cell autolysis than G-NH2, which accounts partially for the different toxicity of the three GNMs. The findings provide significant insights into the mechanism of GNMs toxicity to bacteria for not only the risk assessment of GNMs but also the design of graphene based antibacterial materials.The development of new or upgraded electrochemical water treatment technologies is considered a topic of great interest. Here, Tartrazine azo dye solutions were treated by means of a quite innovative dual electrochemical persulfate (S2O82-, PS) activation that combines H2O2 generation at an air-diffusion cathode and anodic oxidation (AO) at a boron-doped diamond (BDD) anode using a stirred tank reactor. This so-called AO-H2O2/PS process was compared to AO with stainless steel cathode, both in 50 mM Na2SO4 medium, finding the oxidation power increasing as AO less then AO-H2O2 less then AO/PS less then AO-H2O2/PS. In the latter, the dye and its products were mainly destroyed by (i) hydroxyl radicals, formed either from water oxidation at BDD surface or via reaction between H2O2 and S2O82-, and (ii) sulfate radical anion, formed from the latter reaction, thermal PS activation and cathodic S2O82- reduction. NSC 178886 chemical structure Hydroxyl radicals prevailed as oxidizing agents, as deduced from trials with tert-butanol and methanol. The reaction between S2O82- and accumulated H2O2 was favored as temperature increased from 25 to 45 °C. The effect of PS content up to 36 mM, dye concentration within the range 0.22-0.88 mM, current density (j) between 8.3 and 33.3 mA cm-2 and pH between 3.0 and 9.0 on the process performance was examined. All decolorization profiles agreed with a pseudo-first-order kinetics. The best results for treating 0.44 mM dye were attained with 36 mM PS at pH 3.0, j = 16.7 mA cm-2 and 45 °C, yielding total loss of color, 62% TOC removal and 50% mineralization current efficiency after 360 min. The slow mineralization was attributed to the persistence of recalcitrant byproducts like maleic, acetic, oxalic, formic and oxamic acids. It is concluded that the novel AO-H2O2/PS process is more effective than AO/PS to treat Tartrazine solutions, being advisable to extend the study to other organic pollutants.In the last decades, a worldwide increase in dissolved organic carbon (DOC) concentrations has been observed in temperate and boreal lakes. This phenomenon has several detrimental effects on the aquatic life and affect local C geochemical cycles. In this study, we measured DOC concentration in the water column of 36 lakes located in eastern Canada over a period of 35 years (1983-2017) and assessed the influence of climatic, hydrologic and morphometric variables on both DOC concentrations and on the rate of DOC changes (∆DOC). Our data show that morphometric and hydrologic variables have a stronger direct influence on lake water DOC concentrations than vegetation and climatic variables. DOC concentration strongly increased with the drainage ratio and the surface covered by organic deposits, which together explained 59% of the variance. As expected, we observed a significant increase in lake water DOC concentration in 72% of the surveyed lakes, which averaged 20% over the study period. Meanwhile, lake water SO42- concentration decreased by 60%. ∆DOC was poorly influenced by the rate of changes in lake water SO42- as well as by the rate of changes in mean annual air temperature and precipitation. ∆DOC was more related to the vegetation type and the morphometry of the catchment a model including the percentage of conifers, terrestrial catchment area and ∆Cl yielded a variance explanation of 39%. This shows that the rate of increase was primarily driven by morphometric variables which did not change over the study period.Extensive research has focused on the response of vegetation to climate change, including potential mechanisms and resulting impacts. Although many studies have explored the relationship between vegetation and climate change in China, research on spatiotemporal distribution changes of climate regimes using natural vegetation as an indicator is still lacking. Further, limited information is available on the response of vegetation to shifts in China's regional climatic zones. In this study, we applied Mann-Kendall, and correlation analysis to examine the variabilities in temperature, precipitation, surface soil water, normalised difference vegetation index (NDVI), and albedo in China from 1982 to 2012. Our results indicate significant shifts in the distribution of Köppen-Geiger climate classes in China from 12.08% to 18.98% between 1983 and 2012 at a significance level of 0.05 (MK). The percentage areas in the arid and continental zones expanded at a rate of 0.004%/y and 0.12%/y, respectively, while the percentage area in the temperate and alpine zones decreased by -0.