The isotopic composition of organic carbon, nitrogen and provenance of organic matter in surface sediment from the Jiangsu tidal flat, southwestern Yellow Sea.

The Jiangsu tidal flat is a significant organic matter reservoir, but quantitative studies of organic matter sources are scarce. In this study, total organic carbon (TOC) and total nitrogen (TN) concentrations and δ13Corg and δ15Ntotal values of surface sediment from Jiangsu tidal flat were investigated for their distributions, influencing factors, and sources of organic matter. TOC and TN were high in the center of study area and correlated well with grain size, indicating hydrodynamic influence on organic matter. High TOC/TN and low δ13Corg and δ15Ntotal in estuaries were characteristic of C3 plants, soil, and fertilizer sources, suggesting source effect on the distribution of organic matter. The MixSIAR model revealed that marine sources were dominant with a contribution reaching 56.9 %, followed by uniform of C3 plants, soil and fertilizer, while domestic sewage was least prominent. This study enriched theories of the biogeochemical cycle and ecological protection in the southwestern Yellow Sea.

FCF: Feature complement fusion network for detecting COVID-19 through CT scan images.

COVID-19 spreads and contracts people rapidly, to diagnose this disease accurately and timely is essential for quarantine and medical treatment. RT-PCR plays a crucial role in diagnosing the COVID-19, whereas computed tomography (CT) delivers a faster result when combining artificial assistance. Developing a Deep Learning classification model for detecting the COVID-19 through CT images is conducive to assisting doctors in consultation. We proposed a feature complement fusion network (FCF) for detecting COVID-19 through lung CT scan images. This framework can extract both local features and global features by CNN extractor and ViT extractor severally, which successfully complement the deficiency problem of the receptive field of the other. Due to the attention mechanism in our designed feature complement Transformer (FCT), extracted local and global feature embeddings achieve a better representation. We combined a supervised with a weakly supervised strategy to train our model, which can promote CNN to guide the VIT to converge faster. Finally, we got a 99.34% accuracy on our test set, which surpasses the current state-of-art popular classification model. Moreover, this proposed structure can easily extend to other classification tasks when changing other proper extractors.

Capillin protects against non-alcoholic steatohepatitis through suppressing NLRP3 inflammasome activation and oxidative stress.

BACKGROUND: Non-alcoholic steatohepatitis (NASH) is an extreme form of non-alcoholic fatty liver disease. The present study concentrated on the role of Capillin, a polyacetylene compound isolated from Artemisia capillaris Thunb., in NASH development. MATERIALS AND METHODS: Palmitic acid (PA) was treated with FL83B hepatocytes, and high-fat diet was given to mouse to construct the NASH model in vivo. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method, flow cytometry, and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay were carried out to measure the viability and apoptosis of FL83B hepatocytes. Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was performed to measure the mRNA expressions of infiltration markers (Cd11c, Ccr2, and Ly6c), fibrosis genes (Tgfß1, Col1a1, and Timp1), and alpha-smooth muscle actin (α-SMA). Western blot, immunofluorescence, and Enzyme-linked immunosorbent assay (ELISA) were implemented to examine the proteins of Caspase-3, Bcl2, Nrf2, HO-1, NLRP3, ASC, and Caspase-1, the ROS level, and oxidative stress markers (MDA, GSH-ST, SOD, and GSH-Px), and the lipid peroxidation level, respectively. Moreover, HE staining was manipulated to observe the histopathological changes in liver tissue. RESULTS: Capillin hampered PA-mediated hepatocytes apoptosis and enhanced cell viability. Furthermore, Capillin suppressed PA-mediated oxidative stress in hepatocytes, promoted Nrf2/HO-1 expression, and repressed NLRP3-ASC-Caspase1 inflammasome. The in vivo studies indicated that Capillin vigorously improves liver fat accumulation, oxidative stress, and liver injury in NASH mice. Mechanistically, Capillin repressed NLRP3-ASC-Caspase1 inflammasome and up-regulated the Nrf2-HO-1 pathway in the liver. CONCLUSION: Capillin ameliorates hepatocyte injury by dampening oxidative stress and repressing NLRP3 inflammasome in NASH mice.

Synthetic NiO catalyst-assisted peroxymonosulfate for degradation of benzoic acid from aqueous solution.

A heterogeneous NiO catalyst was prepared by a precipitation process using nickel nitrate with oxalic acid and tested for heterogeneous oxidation of benzoic acid (BA) in the presence of peroxymonosulfate (PMS). It was found that the synthetic NiO is highly effective in heterogeneous activation of PMS to produce sulfate radicals ( SO 4 · - ) and hydroxyl radicals (· OH), and also presents stable performance in the heterogeneous activation of PMS for BA degradation. Physicochemical properties of the NiO catalyst were characterized by several techniques, such as thermogravimetric analysis, Brunauer-Emmett-Teller, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. It was found that NiO and NiOOH were formed on the synthetic NiO catalyst and were stably distributed on the catalyst surface. Nearly 95% decomposition could be achieved in 30 min at the conditions of 500 ml 20 µM BA solution, 0.25 g catalyst, and [PMS]:[BA] = 30:1. The heterogeneous reactions, the effects of PMS concentration, and catalyst dosage on the BA degradation were investigated. The heterogeneous BA degradation reactions followed first-order kinetics. Additionally, quenching experiments proved that the dominant radical in the solution was · OH. The experiments results also showed that this approach is effective for the degradation of many other pollutants (such as tetracycline hydrochloride, 2, 4-dichlorophenol, Acid orange 7, rhodamine B, and methyl red). PRACTITIONER POINTS: A novel NiO material was fabricated for degradation of benzoic acid. The synthetic NiO catalyst comprised active NiO and NiOOH. The main radical for benzoic acid removal rate was · OH. A plausible mechanism for catalyzed degradation of the benzoic acid was proposed.

Complete chloroplast genome of an endangered endemic tree, handeliodendron bodinieri (levl.) rehder (sapindaceae) from karst forests of southwest China.

Handeliodendron bodinieri (Sapindaceae) is an endangered monotypic species endemic to the karst forests in southwest China whose populations are now fragmented and the total number of individuals evidently decreased. In this research, we characterized the chloroplast (cp) genome of H. bodinieri using genome skimming. The whole cp genome was 155,291 bp long and comprised 137 genes, including 8 unique rRNAs, 40 tRNAs, and 89 protein-coding genes. The overall guanine-cytosine content of H. bodinieri cp genome was 37.8%. The phylogenetic analysis suggested that H. bodinieri is closely related to the genus Mangifera. This study will be useful for future studies on conservation genetics of this economically important endemic plant.

Generation of reactive oxygen species by promoting the Cu(II)/Cu(I) redox cycle with reducing agents in aerobic aqueous solution.

This study investigated the generation of reactive oxygen species (ROS) (O2 -•, H2O2, and HO•) by promoting the Cu(II)/Cu(I) redox cycle with certain reducing agents (RAs) in aerobic aqueous solution, and benzoic acid (BA) was employed as indicator for the hydroxyl radical (HO•). Hydroxylamine (HA) can reduce Cu(II) to Cu(I) to induce chain reactions of copper species resulting in the generation of the superoxide radical (O2 -•) and hydrogen peroxide (H2O2), and the intermediate Cu(I) can further activate H2O2 via a Fenton-like reaction to produce HO•, creating the remarkable BA degradation. O2 is indispensable, and unprotonated HA is the motive power in the O2/Cu/HA system. Moreover, pH is a crucial factor of the O2/Cu/HA system due to the protonated HA not being able to reduce Cu(II) into Cu(I). The oxidation of HA can be effectively induced by trace amounts of Cu(II), and both a higher HA dosage and a higher Cu(II) dosage can enhance H2O2 generation and BA degradation. In addition, some other RAs that can reduce Cu(II) into Cu(I) could replace HA in the O2/Cu/HA system to induce the generation of these ROS in aerobic aqueous solution.

Degradation of 2,4-dichlorophenol by activating persulfate and peroxomonosulfate using micron or nanoscale zero-valent copper.

The ability of persulfate (PS) and peroxymonosulfate (PMS) activated by micron or nanoscale zero-valent copper (ZVC or nZVC) to degrade 2,4-dichlorophenol (2,4-DCP) was quantified under various conditions. Mechanism investigation revealed that PS and PMS accelerated the corrosion of ZVC or nZVC to release Cu+ under acidic conditions. The in-situ generated Cu+ further decomposed PS or PMS to produce SO4- and OH, which then dramatically degraded 2,4-DCP. The kobs for 2,4-DCP removal followed pseudo-first-order kinetics, kobs of ZVC/PMS and nZVC/PMS systems were 10∼30 times greater than these in ZVC/PS and nZVC/PS systems. The nZVC/PMS system was most effective to remove 2,4-DCP which even did better than the nZVI/PMS system, with rate constant values ranging from 0.041 to 1.855min-1. At higher pH ZVC is ineffective, but nZVC can activate PS and PMS to significantly degrade 2,4-DCP at pH up to 7.3. The 2,4-DCP degradation pathway was found to involve dechloridation, dehydrogenation, hydroxylation, ring open and mineralization. 56.7% and 45.3% of TOC removals were respectively obtained in the ZVC/PMS and nZVC/PMS systems within 120min. This study helps to comprehend the application of zero-valent metals in reactive radicals-based oxidation processes and the reactivity of Cu+ as an activator of PS and PMS.

Ultrasound enhanced heterogeneous activation of peroxymonosulfate by a Co-NiOx catalyst.

Sulfate radical-based advanced oxidation processes have had considerable attention due to the highly oxidizing function of sulfate radicals (SO4-·) resulting in acceleration of organic pollutants degradation in aqueous environments. A Co-Ni mixed oxide nanocatalyst, which was prepared by the sol-gel method, was employed to activate peroxymonosulfate (PMS, HSO5-) to produce SO4-· with Acid Orange 7 (AO7) selected as a radical probe. The catalyst was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). The characterization results indicated that the ingredient of the catalyst had been changed and the amount of surface hydroxyl increased significantly with the addition of Ni. Therefore, it proved that Co-NiOx catalyst was more effective than CoOx to activate PMS. Moreover, ultrasound (US) can increase the degradation rate of AO7 and US/Co-NiOx/PMS system. This study also focused on some synthesis parameters and the system reached the maximum efficiency under the condition when [PMS] = 0.4 mM, [catalyst] = 0.28 g/L, Pus = 200 W. The AO7 removal in these systems follows first order kinetics. Last but not least, quenching studies was conducted which indicated that the amount of hydroxyl radicals (·OH) increases with the increase of initial pH and SO4-· was the primary reactive oxidant for AO7 degradation.

Radicals induced from peroxomonosulfate by nanoscale zero-valent copper in the acidic solution.

A highly efficient advanced oxidation process for the degradation of benzoic acid (BA) during activation of peroxomonosulfate (PMS) by nanoscale zero-valent copper (nZVC) in acidic solution is reported. BA degradation was almost completely achieved after 10 min in the nZVC/PMS process at initial pH 3.0. PMS could accelerate the corrosion of nZVC in acidic to release Cu+ which can further activate PMS to produce reactive radicals. Both sulfate radical (SO4-•) and hydroxyl radical (•OH) were considered as the primary reactive oxidant in the nZVC/PMS process with the experiments of methyl (MA) and tert-butyl alcohol quenching. Acidic condition (initial pH ≤ 3.0) facilitated BA degradation and pH is a decisive factor to affect the oxidation capacity in the nZVC/PMS process. Moreover, BA degradation in the nZVC/PMS process followed the pseudo-first-order kinetics, and BA degradation efficiency increased with the increase of the nZVC dosage.