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Background: Mean perfusion pressure (MPP) has recently emerged as a potential biomarker for personalized management of tissue perfusion in critically ill patients. However, its association with the occurrence of acute kidney injury (AKI) in septic patients and the optimal MPP range remain uncertain. Therefore, this study aims to investigate the relationship between MPP and AKI in critically ill patients with sepsis. Methods: We identified 5867 patients with sepsis from the MIMIC-IV database who met the inclusion and exclusion criteria. The exposure variable was the first set of MPP measured within 24 h after ICU admission with invasive hemodynamic monitoring. The primary outcome was the incidence of AKI at 7 days following ICU admission according to the Kidney Disease: Improving Global Outcomes (KDIGO) guidelines. Secondary outcomes included in-hospital mortality, lengths of ICU, and hospital stay. Optimal cut-off point for MPP were determined using the Youden index, and multivariable logistic regression was employed to examine the association between MPP and AKI. Subgroup analyses were conducted to enhance result robustness. Kaplan-Meier survival analysis was utilized to evaluate in-hospital mortality rates categorized by MPP. Results: A total of 5,867 patients with sepsis were included in this study, and the overall incidence of AKI was 82.3%(4828/5867). Patients were categorized into low MPP (< 63 mmHg) and high MPP (≥ 63 mmHg) groups using the optimal ROC curve-derived cut-off point. The incidence of AKI in the low MPP group was higher than that in the high MPP group (87.6% vs. 78.3%, P < 0.001). Multivariable logistic regression analysis adjusted for confounding factors revealed that each 1 mmHg increase in MPP as a continuous variable was associated with a 2% decrease in AKI incidence within 7 days of ICU admission (OR:0.98, 95%CI:0.97–0.99, P < 0.001). When MPP was used as a categorical variable, patients in the high MPP group had a lower risk of AKI than those in the low MPP group (OR:0.71, 95%CI:0.61–0.83, P = 0.001). Subgroup analyses demonstrated a consistent association between MPP and AKI risk across all variables assessed (P for interaction all > 0.05). Kaplan-Meier curve analysis demonstrated a higher survival rate during hospitalization in the high MPP group compared to the low MPP group (Log-rank test, P < 0.0001). Conclusions: Lower levels of MPP are associated with an increased incidence of AKI at 7 days in critically ill patients with sepsis. [ABSTRACT FROM AUTHOR]

The widespread occurrence of emerging brominated flame retardant tetrabromobisphenol S (TBBPS) has become a major environmental concern. In this study, a nanoscale zero-valent iron (nZVI) impregnated organic montmorillonite composite (nZVI-OMT) was successfully prepared and utilized to degrade TBBPS in aqueous solution. The results show that the nZVI-OMT composite was very stable and reusable as the nZVI was well dispersed on the organic montmorillonite. Organic montmorillonite clay layers provide a strong support, facilitate well dispersion of the nZVI chains, and accelerate the overall TBBPS transformation with a degradation rate constant 5.5 times higher than that of the original nZVI. Four major intermediates, including tribromobisphenol S (tri-BBPS), dibromobisphenol S (di-BBPS), bromobisphenol S (BBPS), and bisphenol S (BPS), were detected by high-resolution mass spectrometry (HRMS), indicating sequential reductive debromination of TBBPS mediated by nZVI-OMT. The effective elimination of acute ecotoxicity predicted by toxicity analysis also suggests that the debromination process is a safe and viable option for the treatment of TBBPS. Our results have shown for the first time that TBBPS can be rapidly degraded by an nZVI-OMT composite, expanding the potential use of clay-supported nZVI composites as an environmentally friendly material for wastewater treatment and groundwater remediation. [ABSTRACT FROM AUTHOR]

Air pollution in the developed regions of eastern China has been intensively investigated in the past decade. However, there is a relative dearth of air pollution studies on the northwest of inland China (e.g., Xinjiang). In this work, hourly measurement data of six criteria air pollutants (PM2.5, PM10, CO, NO2, O3, and SO2) for the past five years (2018–2022) from Hami and Turpan cities of eastern Xinjiang were analyzed to reveal air pollution characteristics and the distribution of potential sources. Hami and Turpan had the highest AQI values in winter due to increased coal combustion for domestic heating and unfavorable meteorological conditions. The slight elevations of AQI values in spring were caused by frequent dust storms. PM10 was the most frequent main pollutant in both Hami (63.1%) and Turpan (74.1%), followed by PM2.5 and O3. Except for O3, PM2.5, PM10, SO2, NO2, and CO exhibited a generally decreasing pattern in annual average values. But the annual average concentrations of PM10 in Hami (83.5 μg·m−3) and Turpan (139 μg·m−3) in 2022 were still higher than those in eastern China. Diurnal and monthly variations of the six criteria pollutants were influenced by a combination of emission sources and meteorological conditions. The air masses in eastern Xinjiang mainly originated from the west and north and were affected by both inter-regional and intra-regional transport. Analysis of the distribution of potential sources showed that local emissions strongly impacted particulate matter pollution in winter, while regional transport played a dominant role in other seasons. O3 showed a broad distribution of potential sources across all four seasons. Considering that the trend that O3 pollution increased year by year, eastern Xinjiang might face a similar pollution situation as eastern China, i.e., the combined pollution of particulate matter and O3. [ABSTRACT FROM AUTHOR]

To understand diurnal variations in PM2.5 composition and aerosol extract absorption, PM2.5 samples were collected at intervals of 2 hr from 8:00 to 20:00 and 6 hr from 20:00 to 8:00 (the next day) in northern Nanjing, China, during the winter and summer of 2019–2020 and analyzed for bulk components, organic tracers, and light absorption of water and methanol extracts—a proxy measure of brown carbon (BrC). Diurnal patterns of measured species reflected the influences of primary emissions and atmospheric processes. Light absorption coefficients of water (Abs365,w) and methanol extracts (Abs365,m) at 365 nm shared a similar diurnal profile peaking at 18:00–20:00, generally following changes in biomass burning tracers. However, Abs365,w, Abs365,m, and their normalizations to organic aerosols increased at 14:00–16:00, earlier than that of levoglucosan in the late afternoon, which was attributed to secondarily formed BrC. The methanol extracts showed a less drastic decrease in light absorption at night than the water extracts and elevated absorption efficiency during 2:00–8:00. This is due to the fact that the water‐insoluble OC has a longer lifetime and stronger light absorption than the water‐soluble OC. According to the source apportionment results solved by positive matrix factorization (PMF), biomass burning and secondary formation were the major BrC sources in northern Nanjing, with an average total relative contribution of about 90%. Compared to previous studies, diurnal source cycles were added to the PMF simulations in this work by using time‐resolved speciation data, which avoided misclassification of BrC sources. Plain Language Summary: Light‐absorbing organic carbon (OC), also known as "brown carbon", plays an important role in influencing the Earth's radiative balance. Filter samples of particulate matter with an aerodynamic diameter of less than 2.5 μm (PM2.5) were collected at a resolution of 2 hr from 8:00 to 20:00 and a resolution of 6 hr from 20:00 to 8:00 (the next day) in northern Nanjing, China, during the winter and summer of 2019 and 2020. To understand the diurnal variations of BrC and its sources, each sample was analyzed for bulk components (OC, elemental carbon, and water‐soluble ions), organic molecular markers, and light absorption by BrC, and a receptor model was used to identify potential BrC sources based on PM2.5 composition data. We found that diurnal variations of BrC generally followed changes in concentrations of levoglucosan‐a tracer of biomass burning; the increase in BrC absorption in the early afternoon was caused by secondary formation of BrC chromophores; biomass burning and secondary formation were the main sources of BrC. Time‐resolved measurements of PM2.5 components were rarely used to investigate the diurnal variations of BrC and its sources, which is very important for modeling the climate impact of BrC. Key Points: Diurnal variations in PM2.5 bulk components and organic tracers reflect diurnal cycles of sourcesLight absorption of water and methanol extracts of PM2.5 exhibited a similar diurnal profile that followed changes in levoglucosanShort‐term and high time‐resolved data of organic tracers should be used for source apportionment to avoid misclassification [ABSTRACT FROM AUTHOR]

By developing a nontarget tandem mass spectrometry experiment workflow, we identified the most probable structures of 100 brown carbon (BrC) chromophores in five types of atmospherically relevant samples including ambient aerosols, biomass burning aerosols, road tunnel aerosols, toluene secondary organic aerosol and rainwater. These chromophores were classified into nine groups, that is, 31 nitrophenols, 12 benzoic acids, 11 oxygenated polycyclic aromatic hydrocarbons, 10 phenols, 10 aryl amides/amines, 9 phenylpropene derivatives, 9 coumarins and flavonoids, 5 pyridines, and 3 nitrobenzoic acids. Among them, aryl amides/amine chromophores, which were mostly found in rainwater, were reported for the first time. The identified chromophores accounted for 20.9%–83.5% of total light absorption over 300–400 nm wavelength or total ion intensity in the 5 types of samples. We identified the characteristic chromophore groups in each sample type and identical chromophores among different sample types, especially between the source samples and ambient aerosols. Gas‐particle distribution and diurnal variation of 13 BrC compounds in the atmosphere were measured by an online high‐resolution chemical ionization mass spectrometer equipped with a Filter Inlet for Gases and Aerosols. It was found that gas‐particle distribution of BrC compounds was dictated by their functional group, oxygen and carbon atom numbers. The BrC compounds containing nitro‐group had higher nighttime concentrations, while those without nitro‐group had higher daytime concentrations. Plain Language Summary: Brown carbon chromophores absorb near‐ultraviolet and visible light and thus influence atmospheric radiation and atmospheric chemistry. By developing a nontarget tandem mass spectrometry experiment workflow, we identified the most probable structures of a large diversity of brown carbon (BrC) chromophores in atmospherically relevant samples like ambient aerosols, biomass burning aerosols, road tunnel aerosols, secondary organic aerosol and rainwater. The similarity and difference of BrC chromophores in these samples were investigated, with a focus on exploring the source of the chromophores in ambient aerosols. For the first time, an online high‐resolution chemical ionization mass spectrometer was applied to measure gas‐particle distribution and diurnal variation of BrC chromophores in the atmosphere. Key Points: We developed a nontarget tandem mass spectrometry experiment workflow to identify the most probable structures of brown carbon (BrC) chromophoresWe identified 100 BrC chromophores in five types of atmospheric samples, among which 33 chromophores was reported for the first timeFilter Inlet for Gases and Aerosols‐chemical ionization mass spectrometer was applied to measure gas‐particle distribution and diurnal variation of BrC chromophores in the atmosphere [ABSTRACT FROM AUTHOR]

The methanol extraction method was widely applied to isolate organic carbon (OC) from ambient aerosols, followed by measurements of brown carbon (BrC) absorption. However, undissolved OC fractions will lead to underestimated BrC absorption. In this work, water, methanol (MeOH), MeOH / dichloromethane (MeOH / DCM, 1:1 , v/v), MeOH / DCM (1:2 , v/v), tetrahydrofuran (THF), and N,N-dimethylformamide (DMF) were tested for extraction efficiencies of ambient OC, and the light absorption of individual solvent extracts was determined. Among the five solvents and solvent mixtures, DMF dissolved the highest fractions of ambient OC (up to ∼95 %), followed by MeOH and MeOH / DCM mixtures (<90 %), and the DMF extracts had significantly (p<0.05) higher light absorption than other solvent extracts. This is because the OC fractions evaporating at higher temperatures (>280 ∘) are less soluble in MeOH (∼80 %) than in DMF (∼90 %) and contain stronger light-absorbing chromophores. Moreover, the light absorption of DMF and MeOH extracts of collocated aerosol samples in Nanjing showed consistent temporal variations in winter when biomass burning dominated BrC absorption, while the average light absorption of DMF extracts was more than 2 times greater than the MeOH extracts in late spring and summer. The average light absorption coefficient at 365 nm of DMF extracts was 30.7 % higher (p<0.01) than that of MeOH extracts. Source apportionment results indicated that the MeOH solubility of BrC associated with biomass burning, lubricating oil combustion, and coal combustion is similar to their DMF solubility. The BrC linked with unburned fossil fuels and polymerization processes of aerosol organics was less soluble in MeOH than in DMF, which was likely the main reason for the large difference in time series between MeOH and DMF extract absorption. These results highlight the importance of testing different solvents to investigate the structures and light absorption of BrC, particularly for the low-volatility fraction potentially originating from non-combustion sources. [ABSTRACT FROM AUTHOR]

Purpose: The number of neuroendocrine tumors (NETs) is gradually increasing worldwide, and those located in the small intestine (siNETs) are the most common. As some biological and clinical characteristics of tumors of the jejunum and the ileum differ, there is a need to assess the prognosis of individuals with siNETs of the jejunum and ileum separately. We generated a predictive nomogram by assessing individuals with siNETs from the Surveillance, Epidemiology, and End Results (SEER) database. Methods: We used univariate Cox regression analysis to determine both the overall survival (OS) and the cancer-specific survival (CSS) of 2501 patients with a pathological confirmation of siNETs of the jejunum and ileum. To predict 3-, 5-, and 10-year OS of siNETs, a nomogram was generated based on a training cohort and validated with an external cohort. Accuracy and clinical practicability were evaluated separately by Harrell's C-indices, calibration plots, and decision curves. The correlation was examined between dissected lymph nodes and positive lymph nodes. Results: Dissection of 7 or more lymph nodes significantly improved patient OS and was found to be a protective factor for patients with siNETs. In Cox regression analyses, age, primary site, tumor size, N stage, M stage, and regional lymph node examination were significant predictors in the nomogram. A significant positive correlation was found between dissected lymph nodes and positive lymph nodes. Conclusions: Patients with 7 or more dissected lymph nodes showed an accurate tumor stage and a better prognosis. Our nomogram accurately predicted the OS of patients with siNETs. [ABSTRACT FROM AUTHOR]

In this study, collocated filter samples of particulate matter with aerodynamic diameter less than 2.5 μm (PM2.5) from northern Nanjing were extracted using water and methanol, followed by analysis of light absorption. A backup quartz filter was used to correct sampling artifacts caused by adsorption of gaseous organics. The collocated precision of light‐absorbing properties of water‐soluble organic carbon (WSOC) and methanol‐extractable organic carbon (MEOC) were parameterized using correlation coefficient (r), coefficient of divergence (COD), and average relative percent difference (ARPD, %). In general, the light absorption of WSOC and MEOC showed good agreement (r > 0.80, COD < 0.20) between collocated samples. Performing artifact correction is necessary and will increase the heterogeneity between collocated measurements. The duplicate‐derived ARPD values of MEOC absorption were more than 60% higher than those of WSOC absorption. Then, it would be inappropriate to assume a uniform uncertainty fraction (e.g., ∼10%) for WSOC and MEOC absorption in future studies on their climate effects and source apportionment. To apportion artifact‐corrected absorption of aerosol extracts to specific emission sources or formation pathways, positive matrix factorization was performed by using concentration data of selected bulk species and organic molecular markers. Among the nine identified factor/sources, the biomass burning factor had the highest average contributions to the absorption of both WSOC (31.6%) and MEOC (48.0%), followed by dust resuspension and coal combustion factors. Unlike combustion‐related primary emissions, the factors containing influences from atmospheric processing (e.g., secondary nitrate) contributed more fractions of WSOC absorption than MEOC absorption. Key Points: Collocated measurements provide an approach to estimate uncertainties in light‐absorbing properties of solvent‐extractable organic carbonIgnoring the adsorption of gaseous organics onto filter medium will lead to significant overestimation of brown carbon absorptionAerosol sources influenced by aging processes contributed more fractions of aqueous extracts absorption than methanol extracts absorption [ABSTRACT FROM AUTHOR]

This study seeks to understand the ambient levels, gas/particle partitioning, and sources of nonpolar organic molecular makers (OMMs) at a suburban site in Nanjing, China. Particle‐ and gas‐phase OMMs were collected using a medium volume sampler equipped with two quartz filters in series and a polyurethane foam (PUF)/XAD‐4/PUF (PXP) adsorbent sandwich. More than 100 pairs of filter and PXP samples were collected diurnally from September 2018 to September 2019. The concentration profiles of total n‐alkanes and polycyclic aromatic hydrocarbons were peaking at n‐C12–n‐C17 homologs (9.98 ± 5.43–38.4 ± 17.7 ng m−3) and naphthalene (92.5 ± 56.7 ng m−3), respectively, followed by decreasing concentrations with further increases in molecular weight. Three artifact correction methods with different pre‐assumptions on relative contributions of evaporation loss to backup filter measurements were used to separate particle‐ and gas‐phase OMMs. The resulting particle‐phase fractions showed significant differences for OMMs with vapor pressure <10−9 atm at 298.15 K. Absorptive gas/particle partitioning coefficients of OMMs were empirically calculated based on measurements and theoretically predicted for comparison. The results obtained under the three artifact correction methods suggested growing importance of evaporation loss with decreased vapor pressure. Positive matrix factorization (PMF) was performed for source apportionment using total (PMFtotal) and particle‐phase (PMFparticle) OMMs data, respectively. Besides eliminating the influence of gas/particle partitioning, the involvements of more volatile species and gaseous OMMs data improved the identification of specific emission sources, supporting the usage of total OMMs data over a wide vapor pressure range for PMF source apportionment. Key Points: The particulate fractions of organic molecular markers attained their minima in summer, when the total concentrations increasedEvaporation loss might be the main sampling artifact of particulate organics when the vapor pressure is lower than 10−10 atmTotal concentrations of organic molecular markers over a wide vapor pressure range should be used for positive matrix factorization analysis [ABSTRACT FROM AUTHOR]

Gas–particle partitioning of water-soluble organic compounds plays a significant role in influencing the formation, transport, and lifetime of organic aerosols in the atmosphere, but is poorly characterized. In this work, gas- and particle-phase concentrations of isoprene oxidation products (C5-alkene triols and 2-methylterols), levoglucosan, and sugar polyols were measured simultaneously at a suburban site of the western Yangtze River Delta in east China. All target polyols were primarily distributed into the particle phase (85.9 %–99.8 %). Given the uncertainties in measurements and vapor pressure predictions, a dependence of particle-phase fractions on vapor pressures cannot be determined. To explore the impact of aerosol liquid water on gas–particle partitioning of polyol tracers, three partitioning schemes (Cases 1–3) were proposed based on equilibriums of gas vs. organic and aqueous phases in aerosols. If particulate organic matter (OM) is presumed as the only absorbing phase (Case 1), the measurement-based absorptive partitioning coefficients (Kp,OMm) of isoprene oxidation products and levoglucosan were more than 10 times greater than predicted values (Kp,OMt). The agreement between Kp,OMm and Kp,OMt was substantially improved when solubility in a separate aqueous phase was included, whenever water-soluble and water-insoluble OM partitioned into separate (Case 2) or single (Case 3) liquid phases, suggesting that the partitioning of polyol tracers into the aqueous phase in aerosols should not be ignored. The measurement-based effective Henry's law coefficients (KH,em) of polyol tracers were orders of magnitude higher than their predicted values in pure water (KH,wt). Due to the moderate correlations between log⁡(KH,em/KH,wt) and molality of sulfate ions, the gap between KH,em and KH,wt of polyol tracers could not be fully parameterized by the equation defining "salting-in" effects and might be ascribed to mechanisms of reactive uptake, aqueous phase reaction, "like-dissolves-like" principle, etc. These study results also partly reveal the discrepancy between observation and modeling of organic aerosols. [ABSTRACT FROM AUTHOR]

Acetaminophen (APAP) is a widely applied drug for the alleviation of pain and fever, which is also a dose‐depedent toxin. APAP‐induced acute liver injury has become one of the primary causes of liver failure which is an increasingly serious threat to human health. Neutrophils are the major immune cells in human serving as the first barrier against the invasion of pathogen. It has been reported that neutrophils patriciate in the occurrence and development of APAP‐induced liver injury. However, evolving evidences suggest that neutrophils also contribute to tissue repair and actively orchestrate resolution of inflammation. Here, we addressed the complex roles in APAP‐induced liver injury on the basis of brief introduction of neutrophil's activation, recruitment and migration. [ABSTRACT FROM AUTHOR]

Hepatitis B virus (HBV) infection is a major public health problem. The high levels of HBV DNA and HBsAg are positively associated with the development of secondary liver diseases, including hepatocellular carcinoma (HCC). Current treatment with nucleos(t)ide analogues mainly reduces viral DNA, but has minimal, if any, inhibitory effect on the viral antigen. Although IFN reduces both HBV DNA and HBsAg, the serious associated side effects limit its use in clinic. Thus, there is an urgent demanding for novel anti‐HBV therapy. In our study, viral parameters were determined in the supernatant of HepG2.2.15 cells, HBV‐expressing Huh7 and HepG2 cells which transfected with HBV plasmids and in the serum of HBV mouse models with hydrodynamic injection of pAAV‐HBV1.2 plasmid. RT‐qPCR and Southern blot were performed to detect 35kb mRNA and cccDNA. RT‐qPCR, Luciferase assay and Western blot were used to determine anti‐HBV effects of MLN4924 and the underlying mechanisms. We found that treatment with MLN4924, the first‐in‐class neddylation inhibitor currently in several phase II clinical trials for anti‐cancer application, effectively suppressed production of HBV DNA, HBsAg, 3.5kb HBV RNA as well as cccDNA. Mechanistically, MLN4924 blocks cullin neddylation and activates ERK to suppress the expression of several transcription factors required for HBV replication, including HNF1α, C/EBPα and HNF4α, leading to an effective blockage in the production of cccDNA and HBV antigen. Our study revealed that neddylation inhibitor MLN4924 has impressive anti‐HBV activity by inhibiting HBV replication, thus providing sound rationale for future MLN4924 clinical trial as a novel anti‐HBV therapy. [ABSTRACT FROM AUTHOR]

N-containing aromatic compounds (NACs) are an important group of light-absorbing molecules in the atmosphere. They are often observed in combustion emissions, but their chemical formulas and structural characteristics remain uncertain. In this study, red oakwood and charcoal fuels were burned in cookstoves using the standard water-boiling test (WBT) procedure. Submicron aerosol particles in the cookstove emissions were collected using quartz (Qf) and polytetrafluoroethylene (PTFE) filter membranes positioned in parallel. A backup quartz filter (Qb) was also installed downstream of the PTFE filter to evaluate the effect of sampling artifacts on NAC measurements. Liquid chromatography–mass spectroscopy (LC–MS) techniques identified 17 NAC chemical formulas in the cookstove emissions. The average concentrations of total NACs in Qb samples (0.37±0.31 – 1.79±0.77 µgm-3) were greater than 50 % of those observed in the Qf samples (0.51±0.43 – 3.91±2.06 µgm-3), and the Qb -to- Qf mass ratios of individual NACs had a range of 0.02–2.71, indicating that the identified NACs might have substantial fractions remaining in the gas phase. In comparison to other sources, cookstove emissions from red oak or charcoal fuels did not exhibit unique NAC structural features but had distinct NAC composition. However, before identifying NAC sources by combining their structural and compositional information, the gas-particle partitioning behaviors of NACs should be further investigated. The average contributions of total NACs to the light absorption of organic matter at λ=365 nm (1.10 %–2.57 %) in Qf and Qb samples (10.7 %–21.0 %) are up to 10 times larger than their mass contributions (Qf : 0.31 %–1.01 %; Qb : 1.08 %–3.31 %), so the identified NACs are mostly strong light absorbers. To explain more sample extract absorption, future research is needed to understand the chemical and optical properties of high-molecular-weight (e.g., molecular weight, MW>500 Da) entities in particulate matter. [ABSTRACT FROM AUTHOR]

Adhesively bonded CFRP/Al joints have been widely used in various engineering fields. However, the poor interface adhesion between the adhesive and the Al adherend limits its further use. In this study, ultrasonic vibration was applied to promote the interface adhesion, and the promotion mechanism was studied in detail. The vibration was exerted on the surface close to the bonding area after the adhesive was applied. According to the bonding strength test, this process improved the bonding strength and repeatability by approximately 32% and 48%, respectively. By comparing the failure behavior without and with ultrasound, it can be seen that ultrasound promotes interface adhesion of the adhesive/Al adherend significantly. Under the application of ultrasonic vibration, a tight microscopic bond was formed at the bonding interface, and a chemical reaction occurred to form chemical bonds. The opening of the epoxy group was promoted to allow Al to react with –O–C to form Al–O–C, because attack of electrophilic Al + on O– of the epoxy group was strengthened by high-frequency impact between the adhesive and the Al adherend at the interface caused by the ultrasonic vibration. It can be seen that the application of ultrasonic vibration during the adhesive bonding process can promote interface adhesion between Al and the adhesive in terms of physics and chemistry, thus significantly improving the performance of the adhesive bond. [ABSTRACT FROM AUTHOR]

Ammonia control has received increasing attention as a measure to decrease particulate concentrations. Modeling analysis of observation data from central China over the period of September 2015 to August 2016 shows clear asymmetric responses of particulate pH and mass to ammonia emissions. With a change of ±80% of NHx (NH3 + NH4+), the corresponding ΔpH are +0.5 and −3.0, respectively, and the corresponding particulate NH4+ changes are +2.62% and −61.8%, respectively. This asymmetry implies that there is a Critical Total Ammonia Concentration, above which particulate pH and mass are insensitive to ammonia control. Analysis of the observation data suggests that the Critical Total Ammonia Concentration is −25%. The estimated cost for an NHx reduction of 25% is $140 – 320 million for Hubei province, which is the initial cost barrier before ammonia control can effectively affect particulate pH and mass in central China. This cost barrier will increase as NOx and SO2 emissions decrease. Key Points: Only after NHx reduction exceeds 25% can ammonia control effectively reduce the inorganic aerosol massMore NHx reduction will be required to reach the critical point of effective ammonia control as NOx and SO2 emissions decreaseA large enough NHx reduction (60%–80%) renders concurrent reduction of NOx emissions ineffective and even the effect of SO2 emission control is reduced [ABSTRACT FROM AUTHOR]

Intense new particle formation (NPF) events were observed in the coastal atmosphere during algae growth and farming season at Xiangshan gulf of the east China coast. High nucleation-mode iodine concentrations measured by ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC/Q-TOF-MS) confirmed that the NPF events were induced by iodine species. Our study provides important information on iodine speciation, size distributions, and its role in NPF in the context of heavy air pollution in China's coastal areas. For the first time, we identified 5 inorganic iodine species, 45 organic iodine compounds (35 molecular formulas), and a group of iodide–organic adducts in aerosols. The concentrations and size distributions of iodine species down to 10 nm were measured during the iodine-induced NPF, continental NPF, and non-NPF days at the coastal site and compared to those at an inland site. The iodine in the above four aerosol sample types were characterized by iodate, aromatic iodine compounds, iodoacetic acid or iodopropenoic acid, and iodide–organic adducts, respectively. Iodide and organic iodine compounds were found in the nucleation-mode particles; however, it is still not clear whether they contributed to nucleation or just new particle growth. Wild algae, as well as farmed algae, could be an important NPF source in China's coastal areas. [ABSTRACT FROM AUTHOR]

This study seeks to understand the compositional details of N-containing aromatic compounds (NACs) emitted during biomass burning (BB) and their contribution to light-absorbing organic carbon (OC), also termed brown carbon (BrC). Three laboratory BB experiments were conducted with two United States pine forest understory fuels typical of those consumed during prescribed fires. During the experiments, submicron aerosol particles were collected on filter media and subsequently extracted with methanol and examined for their optical and chemical properties. Significant correlations (p<0.05) were observed between BrC absorption and elemental carbon (EC)/OC ratios for individual burns data. However, the pooled experimental data indicated that EC/OC alone cannot explain the BB BrC absorption. Fourteen NAC formulas were identified in the BB samples, most of which were also observed in simulated secondary organic aerosol (SOA) from photooxidation of aromatic volatile organic compounds (VOCs) with NOx. However, the molecular structures associated with the identical NAC formula from BB and SOA are different. In this work, the identified NACs from BB are featured by methoxy and cyanate groups and are predominately generated during the flaming phase. The mass concentrations of identified NACs were quantified using authentic and surrogate standards, and their contributions to bulk light absorption of solvent-extractable OC were also calculated. The contributions of identified NACs to organic matter (OM) and BrC absorption were significantly higher in flaming-phase samples than those in smoldering-phase samples, and they correlated with the EC/OC ratio (p<0.05) for both individual burns and pooled experimental data, indicating that the formation of NACs from BB largely depends on burn conditions. The average contributions of identified NACs to overall BrC absorption at 365 nm ranged from 0.087±0.024 % to 1.22±0.54 %, which is 3–10 times higher than their mass contributions to OM (0.023±0.0089 % to 0.18±0.067 %), so the NACs with light absorption identified in this work from BB are likely strong BrC chromophores. Further studies are warranted to identify more light-absorbing compounds to explain the unknown fraction (>98 %) of BB BrC absorption. [ABSTRACT FROM AUTHOR]

Atmospheric trace elements, especially metal species, are an emerging environmental and health concern with insufficient understanding of their levels and sources in Shanghai, the most important industrial megacity in China. Here we continuously performed a 1 year (from March 2016 to February 2017) and hourly resolved measurement of 18 elements in fine particles (PM2:5) at the Shanghai urban center with an Xact multi-metals monitor and several collocated instruments. Mass concentrations (mean±1σ; ngm-3) determined by Xact ranged from detection limits (nominally 0.1 to 20 ngm-3) to 15 µgm-3. Element-related oxidized species comprised an appreciable fraction of PM2:5 during all seasons, accounting for 8.3% on average. As a comparison, the atmospheric elements concentration level in Shanghai was comparable with that in other industrialized cities in East Asia but 1 or 2 orders of magnitude higher than at sites in North America and Europe. Positive matrix factorization (PMF) was applied to identify and apportion the sources of the elements in the PM2:5 mass. Five different factors were resolved (notable elements and relative contribution in parentheses): traffic-related (Ca, Fe, Ba, Si; 46%), shipping (V, Ni; 6%), nonferrous metal smelting (Ag, Cd, Au; 15%), coal combustion (As, Se, Hg, Pb; 18%) and ferrous metal smelting (Cr, Mn, Zn; 15%). The contribution from the exhaust and non-exhaust vehicle emissions, i.e., the traffic-related factor shows a strong bimodal diurnal profile with average concentration over 2 times higher during the rush hour than during nighttime. The shipping factor was firmly identified because V and Ni, two recognized tracers of shipping emissions, are almost exclusively transported from the East China Sea and their ratio (around 3.2) falls within the variation range of V= Ni ratios in particles emitted from heavy oil combustion. Interestingly, nearly half of the K was derived from coal combustion with high mineral affinity (elements associated with aluminosilicates, carbonates and other minerals in coal ash). The contributions of nonferrous metal smelting to the trace elements are consistent with a newly developed emission inventory. Although the precipitation scavenging effect on the mass concentration of the trace elements varied among different species and sources, precipitation could effectively lower the concentration of the trafficand coal combustion-related trace elements. Therefore, water spray to simulate natural types of precipitation could be one of the abatement strategies to facilitate the reduction of ambient PM2:5 trace elements in the urban atmosphere. Collectively, our findings in this study provide baseline levels and sources of trace elements with high detail, which are needed for developing effective control strategies to reduce the high risk of acute exposure to atmospheric trace elements in China's megacities. [ABSTRACT FROM AUTHOR]

Bacterial multidrug resistance efflux systems serve an important role in antimicrobial resistance. Thus, identifying novel and effective efflux pump inhibitors that are safe with no adverse side effects is urgently required. Silybin is a flavonolignan component of the extract from the milk thistle seed. To order to investigate the mechanism by which silybin inhibits the efflux system of methicillin-resistant Staphylococcus aureus (MRSA), antimicrobial susceptibility testing and the double-plate method were used to evaluate the effect of silybin on MRSA41577. The ability of silybin to inhibit the efflux of ciprofloxacin from MRSA was evaluated by performing a fluorescence assay. Reverse transcription-quantitative polymerase chain reaction analysis revealed that silybin reduced the expression of the quinolone resistance protein NorA (norA) and quaternary ammonium resistance proteins A/B (qacA/B) efflux genes in MRSA. This suggested that silybin may effectively inhibit the efflux system of MRSA41577. Compared with the control, MRSA41577 treated with silybin for 16 h exhibited a 36 and 49% reduction in the expression of norA and qacA/B, respectively. Inhibition of the expression of these genes by silybin restored the sensitivity of MRSA41577 to antibiotics, indicating that efflux pump inhibitors, which act by inhibiting the efflux system of MRSA, may disrupt the MRSA resistance to antibiotics, rendering the bacteria sensitive to these drugs. [ABSTRACT FROM AUTHOR]

This study investigates the composition of organic particulate matter in PM2.5 in a remote montane forest in the southeastern US, focusing on the role of organic nitrogen (N) in sulfur-containing secondary organic aerosol (nitrooxy-organosulfates) and aerosols associated with biomass burning (nitro-aromatics). Bulk water-soluble organic N (WSON) represented  ∼  14 % w∕w of water-soluble total N (WSTN) in PM2.5 on average across seasonal measurement campaigns conducted in the spring, summer, and fall of 2015. The largest contributions of WSON to WSTN were observed in spring ( ∼  18 % w∕w) and the lowest in the fall ( ∼  10 % w∕w). On average, identified nitro-aromatic and nitrooxy-organosulfate compounds accounted for a small fraction of WSON, ranging from  ∼  1 % in spring to  ∼  4 % in fall, though were observed to contribute as much as 28 % w∕w of WSON in individual samples that were impacted by local biomass burning. The highest concentrations of oxidized organic N species occurred during summer (average of 0.65 ng N m−3) along with a greater relative abundance of higher-generation oxygenated terpenoic acids, indicating an association with more aged aerosol. The highest concentrations of nitro-aromatics (e.g., nitrocatechol and methyl-nitrocatechol), levoglucosan, and aged SOA tracers were observed during fall, associated with aged biomass burning plumes. Nighttime nitrate radical chemistry is the most likely formation pathway for nitrooxy-organosulfates observed at this low NOx site (generally < 1 ppb). Isoprene-derived organosulfate (MW216, 2-methyltetrol derived), which is formed from isoprene epoxydiols (IEPOX) under low NOx conditions, was the most abundant individual organosulfate. Concentration-weighted average WSON ∕ WSOC ratios for nitro-aromatics + organosulfates + terpenoic acids were 1 order of magnitude lower than the overall aerosol WSON ∕ WSOC ratio, indicating the presence of other uncharacterized higher-N-content species. Although nitrooxy-organosulfates and nitro-aromatics contributed a small fraction of WSON, our results provide new insight into the atmospheric formation processes and sources of these largely uncharacterized components of atmospheric organic N, which also helps to advance the atmospheric models to better understand the chemistry and deposition of reactive N. [ABSTRACT FROM AUTHOR]

In this paper, the time series analysis method CLEANest is employed to search for characteristic periodicities in the radio light curves of the blazar NRAO 530 at 4.8, 8.0 and 14.5 GHz over a time baseline of three decades. Two prominent periodicities on time scales of ∼6.3 and ∼9.5 a are identified at all three frequencies, in agreement with previous results derived from different numerical techniques, confirming the multiplicity of the periodicities in NRAO 530. In addition to these two significant periods, there is also evidence of shorter-timescale periodicities of ∼5.0, ∼4.2, ∼3.4 and ∼2.8 a showing lower amplitude in the periodograms. The physical mechanisms responsible for the radio quasi-periodic oscillations and the multiplicity of the periods are discussed. [ABSTRACT FROM AUTHOR]

BSTRACT Primary (i.e. sugars and sugar-alcohols) and secondary (i.e. carboxylic acids) water-soluble organic compounds (WSOCs) in size-segregated aerosols from the urban and mountain atmosphere of China and from the marine atmosphere in the outflow region of East Asia were characterized on a molecular level. Levoglucosan is the most abundant compound among the quantified WSOCs in the urban and mountain atmosphere, whose concentration at the urban site was 1-2 orders of magnitude higher than that at the mountain and marine sites. In contrast, malic, succinic and phthalic acids were dominant among the measured WSOCs at the marine site. In the urban air, sugars except levoglucosan gave a bimodal size distribution with a large peak in fine range (<2.1 μm) and a small peak in coarse range (≥2.1 μm) during winter, being opposite to those in spring. In contrast, these WSOCs at the mountain and marine sites dominated in the coarse range but diminished and even disappeared in the fine range. Geometric mean diameters (GMDs) of the measured WSOCs in the fine mode at the urban site were larger in winter than in spring. Levoglucosan and carboxylic acids except for azelaic and benzoic acids showed a larger GMD in the coarse mode at the marine site probably due to an increased hygroscopic growth. [ABSTRACT FROM AUTHOR]

Recently, the occurrence of fog and haze over China has increased. The retrieval of trace gases from the multi-axis differential optical absorption spectroscopy (MAX-DOAS) is challenging under these conditions. In this study, various reported retrieval settings for formaldehyde (HCHO) and sulfur dioxide (SO2) are compared to evaluate the performance of these settings under different meteorological conditions (clear day, haze, and fog). The dataset from 1st December 2019 to 31st March 2020 over Nanjing, China, is used in this study. The results indicated that for HCHO, the optimal settings were in the 324.5–359 nm wavelength window with a polynomial order of five. At these settings, the fitting and root mean squared (RMS) errors for column density were considerably improved for haze and fog conditions, and the differential slant column densities (DSCDs) showed more accurate values compared to the DSCDs between 336.5 and 359 nm. For SO2, the optimal settings for retrieval were found to be at 307–328 nm with a polynomial order of five. Here, root mean square (RMS) and fitting errors were significantly lower under all conditions. The observed HCHO and SO2 vertical column densities were significantly lower on fog days compared to clear days, reflecting a decreased chemical production of HCHO and aqueous phase oxidation of SO2 in fog droplets. [ABSTRACT FROM AUTHOR]

The emergence of the novel corona virus and the resulting lockdowns over various parts of the world have substantially impacted air quality due to reduced anthropogenic activity. The objective of this study is to investigate the impact of COVID-19 lockdown and Spring Festival on air quality of four major cities of Yangtze River Delta (YRD) region, including Shanghai, Nanjing, Hefei, and Hangzhou. In situ measurements were taken for nitrogen dioxide (NO2), particulate matter (PM2.5) and ozone (O3). In situ measurements from 1 January to 25 April were taken two years prior to COVID-19 (2018–19), during COVID-19 lockdown (2020), and one year after the COVID-19 (2021). The results indicated that the concentration of NO2 and PM2.5 dropped considerably during the lockdown days compared to normal days while the O3 concentration showed an upsurge. The NO2 showed reduction of about 54% on average during lockdown level 1 in 2020 whereas, PM 2.5 showed reduction of about 36% through the YRD. A substantial drop was observed in concentration of NO2 during the Spring Festival holidays throughout the YRD from 2019 to 2021. [ABSTRACT FROM AUTHOR]

The spread of the COVID-19 pandemic and consequent lockdowns all over the world have had various impacts on atmospheric quality. This study aimed to investigate the impact of the lockdown on the air quality of Nanjing, China. The off-axis measurements from state-of-the-art remote-sensing Multi-Axis Differential Optical Absorption Spectroscope (MAX-DOAS) were used to observe the trace gases, i.e., Formaldehyde (HCHO), Nitrogen Dioxide (NO2), and Sulfur Dioxide (SO2), along with the in-situ time series of NO2, SO2 and Ozone (O3). The total dataset covers the span of five months, from 1 December 2019, to 10 May 2020, which comprises of four phases, i.e., the pre lockdown phase (1 December 2019, to 23 January 2020), Phase-1 lockdown (24 January 2020, to 26 February 2020), Phase-2 lockdown (27 February 2020, to 31 March 2020), and post lockdown (1 April 2020, to 10 May 2020). The observed results clearly showed that the concentrations of selected pollutants were lower along with improved air quality during the lockdown periods (Phase-1 and Phase-2) with only the exception of O3, which showed an increasing trend during lockdown. The study concluded that limited anthropogenic activities during the spring festival and lockdown phases improved air quality with a significant reduction of selected trace gases, i.e., NO2 59%, HCHO 38%, and SO2 33%. We also compared our results with 2019 data for available gases. Our results imply that the air pollutants concentration reduction in 2019 during Phase-2 was insignificant, which was due to the business as usual conditions after the Spring Festival (Phase-1) in 2019. In contrast, a significant contamination reduction was observed during Phase-2 in 2020 with the enforcement of a Level-II response in lockdown conditions i.e., the easing of the lockdown situation in some sectors during a specific interval of time. The observed ratio of HCHO to NO2 showed that tropospheric ozone production involved Volatile Organic Compounds (VOC) limited scenarios. [ABSTRACT FROM AUTHOR]

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has spread globally with more than 33 million patients diagnosed, taking more than a million lives. Abundant mutations were observed but the functional consequences of these mutations are largely unknown. We report the mutation spectrum, replication dynamics, and infectivity of 11 patient-derived viral isolates in diverse cell lines, including the human lung cancer cell line Calu-3. We observed 46 mutations, including 9 different mutations in the spike gene. Importantly, these viral isolates show significant and consistent variations in replication dynamics and infectivity in tested cell lines, up to a 1500-fold difference in viral titers at 24 h after infecting Calu-3 cells. Moreover, we show that the variations in viral titers among viral isolates are positively correlated with blood clotting function but inversely correlated with the amount of red blood cell and hemoglobin in patients. Therefore, we provide direct evidence that naturally occurring mutations in SARS-CoV-2 can substantially change its replication dynamics and infectivity in diverse human cell lines, with clinical implications in vivo. [ABSTRACT FROM AUTHOR]

Background: In previous studies, a TiO2 coating was prepared on Ti surface through micro‐arc oxidation (MAO) by using calcium acetate as electrolyte, and the effects of the coating on cell attachment were testified. The main elemental compositions of the MAO coatings can be Ca, P, Ti and O. The Ca and P can promote the adhesion and differentiation of osteoblast. Dandelion polysaccharide is one kind of the active constituent of Taraxacum mongolicum, a Chinese medicinal herb, widespreading in nature. Aim/Hypothesis:This study aimed to investigate the effects of the MAO coating on mesenchymal stem cells while loading with dandelion polysaccharide. Material and Methods: (i) The schistose‐shaped Ti (_I_n_i_ = 15) were supplied. MAO treatment was performed on the machined implants by a MAO equipment. Furthermore, the MAO coating has been loading with 2.0 mg/L dandelion polysaccharide solution. A pure Ti and MAO coating that has been served as control (_I_n_i_ = 15, pure Ti surface = 5, MAO coating surface = 5, MAO coating loading with dandelion polysaccharide). (ii) Scanning electron microscopy was used to observe the Ti surface morphology. The elemental concentrations of the surfaces were quantified by energy dispersive X‐ray spectrometer. The phase composition was analyzed by X‐ray diffraction (iii) BMSCs were seeded on the surface of different groups and cultured. Then CCK‐8 kit was used to detect the adhesion and proliferation at selected time points. (iv) SPSS 20.0 software was used for statistical analysis. Results: (i) The coating with regular microstructure (diameter 1.0–6.0 mm) was prepared by micro‐arc oxidation on titanium substrates. (Fig.1) (ii) At 2 and 4 hours, the number of BMSCs of MAO group and MAO load group are more than Ti group and the difference was statistically significant, but there was no significant difference between the two groups. (Fig.2) (iii) At 3 days, the number of BMSCs of MAO load group are more than Ti group and MAO group, and the difference was statistically significant, while at 5 days and 7 days, there was no significant difference between MAO group and MAO load group. (Fig.3) Conclusions and Clinical Implications:Micro arc oxidation method was used to successfully product a coating rich in calcium and phosphorus elements and loaded with dandelion polysaccharide. (ii) The experiment in vitro showed that dandelion polysaccharide may promote proliferation of BMSCs on the surface of MAO coatings while cannot promote the adhesion.

Hepatocellular carcinoma remains the sixth most lethal malignancy in the world. While HCC is often diagnosed via current biomarkers at a late stage, early detection of HCC has proven to be very difficult. Recent studies have focused on using exosomal miRNAs in clinical diagnostics and therapeutics, because they have improved stability in exosomes than as free miRNAs themselves. Exosomal miRNAs act through novel mechanisms for inducing cellular responses in a variety of biological circumstances. Dysregulated expression of miRNAs in exosomes can also accelerate HCC progression, including cell proliferation and metastasis, via alteration of a network of genes. Growing evidence demonstrates that exosomal miRNAs can affect many aspects of physiological and pathological conditions in HCC and indicates that miRNAs in exosomes can not only serve as sensitive biomarkers for cancer diagnostics and recurrence but can also potentially be used as therapeutics to target HCC progression. In this review, we summarize the latest findings between exosomal miRNAs and HCC, in order to better comprehend the functions and applications in HCC. Moreover, we discuss critical issues to consider when developing anti-tumor exosomal miRNAs as a novel therapeutic strategy for treating HCC in the clinic. [ABSTRACT FROM AUTHOR]

Atmospheric aerosols have been shown to be an important input of organic carbon and nutrients to alpine watersheds and influence biogeochemical processes in these remote settings. For many remote, high elevation watersheds, direct evidence of the sources of water soluble organic aerosols and their chemical and optical characteristics is lacking. Here, we show that the concentration of water soluble organic carbon (WSOC) in the total suspended particulate (TSP) load at a high elevation site in the Colorado Rocky Mountains was strongly correlated with UV absorbance at 254 nm (Abs254, r = 0.88 p < 0.01) and organic carbon (OC, r = 0.95 p < 0.01), accounting for >90% of OC on average. According to source apportionment analysis, biomass burning had the highest contribution (50.3%) to average WSOC concentration; SOA formation and motor vehicle emissions dominated the contribution to WSOC in the summer. The source apportionment and backward trajectory analysis results supported the notion that both wildfire and Colorado Front Range pollution sources contribute to the summertime OC peaks observed in wet deposition at high elevation sites in the Colorado Rocky Mountains. These findings have important implications for water quality in remote, high-elevation, mountain catchments considered to be our pristine reference sites. [ABSTRACT FROM AUTHOR]