Microbial densities, functional genes, and their responses to environment factors have been studied for years, but still a lot remains unknown about their interactions with each other. In this study, the abundances of 7 nitrogen cycling genes in the sediments from Hangzhou Bay were analyzed along with bacterial and archaeal 16S rRNA abundances as the biomarkers of their densities. The amount of organic matter (OM) and total nitrogen (TN) strongly positively correlated with each other and microbial densities, while total phosphate (TP) and ammonia-nitrogen (NH3–N) did not. Most studied genes were density suppressed, while nirS was density stable, and nosZ and hzo were density irrelevant. This suggests eutrophication could limit inorganic nitrogen cycle pathways and the removal of nitrogen in the sediment and emit more greenhouse gases. This study provides a new insight of microbial community structures, functions and their interactions in the sediments of eutrophic bays.
Recent Chinese air pollution actions have significantly lowered the levels of fine particulate matter (PM2.5) in North China via controlling emissions of sulfur dioxide (SO2) and nitrogen oxides (NO x ) together with primary aerosols, while the emissions of another precursor, ammonia (NH3), have not yet been regulated. This raises a question that how effective the NH3 emission controls can be on the mitigation of PM2.5 pollution along with the reduction of SO2 and NO x emissions. Here we use a regional air quality model to investigate this issue focusing on the PM2.5 pollution in North China for January and July 2015. We find that the efficiency of the PM2.5 reduction is highly sensitive to the NH3 emission and its reduction intensity. Reductions in the population-weighted PM2.5 concentration (PWC) in the Beijing–Tianjin–Hebei region are only 1.4–3.8 μg m−3 (1.1%–2.9% of PM2.5) with 20%–40% NH3 emission reductions, but could reach 8.1–26.7 μg m−3 (6.2%–21%) with 60%–100% NH3 emission reductions in January 2015. Besides, the 2015–2017 emission changes (mainly reduction in SO2 emissions) could lower the PM2.5 control efficiency driven by the NH3 reduction by up to 30% for high NH3 emission conditions, while lead to no change or increase in the efficiency when NH3 emissions become low. NO x emission reductions may enhance the wintertime PM2.5 pollution due to the weakened titration effect and can be offset by simultaneously controlling NH3 emissions. Our results emphasize the need to jointly consider NH3 with SO2 and NO x emission controls when designing PM2.5 pollution mitigation strategies.
Existing critical point theories including metric and topological critical point theories are difficult to be applied directly to some concrete problems in particular polyhedral settings, because the notions of critical sets could be either very vague or too large. To overcome these difficulties, we develop critical point theory for nonsmooth but Lipschitzian functions defined on convex polyhedrons. This yields natural extensions of classical results in critical point theory, such as the Liusternik-Schnirelmann multiplicity theorem. More importantly, eigenvectors for some eigenvalue problems involving graph 1-Laplacian coincide with critical points of the corresponding functions on polytopes, which indicates that the critical point theory proposed in the present paper can be applied to study the nonlinear spectral graph theory.
Coinfection of hepatitis B virus (HBV) and hepatitis C virus (HCV) may result in severe liver disease and frequent progression to cirrhosis and hepatocellular carcinoma. Clinical evidence suggests that HBV replication is suppressed by replicating HCV and often rebounds after treatment with drugs against HCV. Thus, a highly efficient cell culture system permissive for HBV/HCV would facilitate investigation on the interaction and pathogenesis after coinfection. Here we reported a robust HBV/HCV coinfection cell culture model by overexpressing human sodium-taurocholate cotransporting polypeptide (NTCP), CD81 and Mir122 into HepG2 cells and investigated interactions between HBV and HCV. In this system, HepG2-NTCP/CD81/Mir122 cells not only supported robust infection and replication of HBV and HCV, but also allowed HBV/HCV coinfection in the single cell level. Our result showed cells with replicating HBV still supported HCV infection. However, HBV replication was suppressed by HCV through the inhibition of HBV core promoter and S promoter II activity, and this inhibition was attenuated by the interferon alpha (IFNα) treatment, suggesting HCV influence on HBV at transcriptional level. Coinfection of HBV/HCV in this system did not block IFN stimulated genes expression. Inhibition of HCV by direct-acting antiviral drugs restored HBV replication and expression of viral genes. Conclusions: HepG2-NTCP/CD81/Mir122 fully supports HBV/HCV coinfection, replication and interaction. This novel cell model offers a platform to advance our understanding of the molecular details of the interaction, pathogenesis and outcomes of HBV/HCV coinfection.
In this study, we designed an integrated electrochemical filtration system for catalytic activation of peroxymonosulfate (PMS) and degradation of aqueous microcontaminants. Composites of carbon nanotube (CNT) and nanoscale zero valence copper (nZVC) were developed to serve as high-performance catalysts, electrode and filtration media simultaneously. We observed both radical and nonradical reaction pathways, which collectively contributed to the degradation of model pollutants. Congo red was completely removed via a single-pass through the nZVCCNT filter (τ <2 s) at neutral pH. The rapid kinetics of Congo red degradation were maintained across a wide pH range (from 3.0–7.0), in complicated matrixes (e.g., tap water and lake water), and for the degradation of a wide array of persistent organic contaminants. The superior activity of nZVCCNT stems from the boosted redox cycles of Cu2+/Cu+ in the presence of an external electric field. The flow-through design remarkably outperformed the conventional batch system due to the convection-enhanced mass transport. Mechanism studies suggested that the carbonyl group and electrophilic oxygen of CNT served as electron donor and electron acceptor, respectively, to activate PMS to generate •OH and 1O2 via one-electron transport. The electron-deficient Cu atoms are prone to react with PMS via surface hydroxyl group to produce reactive intermediates (Cu2+-O-O-SO3−), and then 1O2 will be generated by breaking the coordination bond of the metastable intermediate. The study will provide a green strategy for the remediation of organic pollution by a highly efficient and integrated system based on catalytic oxidation, electrochemistry, and nano-filtration techniques.
It has been suggested that indoor exposure to ozone oxidation products contributes materially to the apparent associations between outdoor ozone concentration and morbidity and mortality. Our current understanding of indoor ozone chemistry derives mainly from studies with test surfaces under controlled conditions. Little is known about the overall impact of ozone chemistry on air composition in dynamically changing indoor residential environments. The results presented here reflect a quantitative characterization of overall indoor ozone chemistry in a normally occupied home. Findings reveal a strong influence of off-body skin lipids on indoor ozone chemistry. Being able to elucidate indoor air pollutants derived from ozone chemistry facilitates the investigation of causal links between outdoor ozone concentrations and adverse health effects.Outdoor ozone transported indoors initiates oxidative chemistry, forming volatile organic products. The influence of ozone chemistry on indoor air composition has not been directly quantified in normally occupied residences. Here, we explore indoor ozone chemistry in a house in California with two adult inhabitants. We utilize space- and time-resolved measurements of ozone and volatile organic compounds (VOCs) acquired over an 8-wk summer campaign. Despite overall low indoor ozone concentrations (mean value of 4.3 ppb) and a relatively low indoor ozone decay constant (1.3 h−1), we identified multiple VOCs exhibiting clear contributions from ozone-initiated chemistry indoors. These chemicals include 6-methyl-5-hepten-2-one (6-MHO), 4-oxopentanal (4-OPA), nonenal, and C8-C12 saturated aldehydes, which are among the commonly reported products from laboratory studies of ozone interactions with indoor surfaces and with human skin lipids. These VOCs together accounted for ≥12% molecular yield with respect to house-wide consumed ozone, with the highest net product yield for nonanal (≥3.5%), followed by 6-MHO (2.7%) and 4-OPA (2.6%). Although 6-MHO and 4-OPA are prominent ozonolysis products of skin lipids (specifically squalene), ozone reaction with the body envelopes of the two occupants in this house are insufficient to explain the observed yields. Relatedly, we observed that ozone-driven chemistry continued to produce 6-MHO and 4-OPA even after the occupants had been away from the house for 5 d. These observations provide evidence that skin lipids transferred to indoor surfaces made substantial contributions to ozone reactivity in the studied house.All study data are included in the article and supporting information.