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Bengbu Ancient Residence Expo Park is named after the collection of ancient buildings in Fujian, Zhejiang, southern Anhui and the Three Gorges reservoir area, and is called the "open-air museum" of Chinese ancient dwellings. From "collection" to "activation", in order to further promote the visual and living inheritance of the park's intangible cultural heritage art, especially to deeply explore the way of the intangible cultural heritage culture of ancient dwellings developing in the same frequency with the new era society, this paper uses a variety of narrative strategies such as serial narration of thematic stories, visual communication, and "ancient dwellings+" tourism culture IP, aiming at activating the charm of ancient dwellings. The "collection and activation" of Chinese ancient dwellings has polished the local characteristic cultural business cards and promoted the ecological development of regional economy.

The purpose of this study is to study the air contaminants in the cabins of underwater vehicle. The basic data help for the better research of the underwater vehicle cabin environment standard and the control strategy. Pretreatment and analysis method of volatile organic compounds was preconcentration combined with gas chromatography under the condition of liquid nitrogen and detected by chromatography-mass spectrometry. The pollution of particles, carbon monoxide and carbon dioxide during the underwater vehicle voyage were monitored by online monitoring instrument. Altogether 34 kinds of pollution components were detected, most of which were low in concentration. Some are low olfactory threshold or high toxic components, such as dimethyldisulfide, benzene, carbon disulfide, trichloromethane, and several reached to ppm level. The contamination of the particles was mainly fine particles and part cabins exceeded the national standard of indoor air quality. The highest concentration of carbon dioxide in accommodation space exceeded the permissible concentration of atmosphere composition aboard diesel underwater vehicle compartments. The increase submerged time made the environment in the cabins deteriorate. The concentration of trace contaminants may close to or beyond the relevant standards with the prolonged time. The volatile organic compounds, particles, carbon monoxide and carbon dioxide aggravated the air circumstance in the cabins. It should be determined the permissible concentration of air contaminants in underwater vehicle as soon as possible.

BACKGROUND: Biological treatment technology is good for the recovery of resources and energy from municipal solid waste (MSW) and cutting down biodegradable components in landfill waste. Recently, the aerobic biological treatment of MSW has increased in rural areas of China. These facilities are usually open setup and closed to nearby residents, and complaints tend to be received regarding odorous gases. A semi-in-vessel setup facility was occured in recent years, and its impact on the environment and personnel is not clear.RESULTS: Ammonia was the predominant compound released from the windrow and its concentration was one order of magnitude higher than those of other compounds. Terpenes and reduced sulfur compounds (RSCs) persisted throughout the entire active fermentation process, with only slight decreases. The biofilter pool had a greater odor impact on the surrounding neighborhood than the waste unloading and sorting operation. The concentrations of most compounds were reduced by the biofilter pool. Ten major substances that caused odors at the periphery of the facility were analyzed, where most comprised RSCs. The odor impact of the facility was low but it was associated with a carcinogenic risk to the operators, thereby indicating the need to improve personal protection.Conclusions: Large amounts of ammonia and volatile organic compounds were released from the composting units, but they had a low odor impact on the environment because of the semi-in-vessel setup. The odor impact of the facility was low but it was associated with a carcinogenic risk to the operators. This technology can be popularized in rural areas.

Highlights • Low-dose and short-term exposure to methyl mercaptan had adverse effects on lung tissue. • Lipid peroxidation and alterations in blood antioxidant enzyme levels were observed following the exposure. • Oxidative damage is recognized as a potential mechanism for pulmonary stimulation and injury. • Malondialdehyde in lung tissue was significantly increased in both males and females exposure group., The present study was carried out to evaluate the hematotoxicity and respiratory toxicity of methyl mercaptan in Sprague-Dawley rats. A dynamic exposure methodology was adopted in this study following 7 days of exposure by repeated inhalation. The concentration of methyl mercaptan used in the exposure was 0.5 ppm and the exposure time was 6 h/day for 7 days. After exposure, the rats were sacrificed to collect lung tissue and blood samples. Routine blood and serum biochemistry were conducted. Morphological injury of lung tissue was detected by hematoxylin and eosin staining. Decreased food consumption and body weight gain in both sexes were noted in the exposure group compared with the control group. Several significant changes in hematological parameters were observed. The results showed that the blood urea nitrogen (UREA) levels and superoxide dismutase (SOD) values were significantly decreased in exposed male rats. Malondialdehyde (MDA) in lung tissue was significantly increased in both males and females in the exposed group. In the histopathological examination of lung tissue, terminal bronchiole constriction, alveolar congestion, and erythrocyte exudation were observed, suggesting that the lungs may be target organs after inhaling methyl mercaptan and workers exposed to this concentration may cause some pulmonary stimulation and injury.

The objective of the research was to reveal the potential toxicity effects of methyl mercaptan on rat lung tissue. A dynamic exposure device and Sprague-Dawley (SD) rats were adopted. The exposure concentration of methyl mercaptan was 0.5 ± 0.1 ppm. The exposure procedure was 6 h/day, continuing for 30 days. The routine blood levels, oxidative stress levels in serum, immune molecule and cytokine in the serum and lung tissue were tested. Morphology injury of lung tissue was detected by Hematoxylin and Eosin (HE) staining. Apoptosis rate of alveolar epithelial cells were determined by TdT-mediated dUTP Nick End Labeling (TUNEL) assay. Reduction of body weight gain was observed in the male group during the exposure time, while there was no significant reduction of body weight gain in the female group. Pathological findings of terminal bronchiole constriction, alveolar congestion, and erythrocyte exudation confirmed the lung to be the main target organ. An apparent pneumonocyte apoptotic effection was also observed. Oxidative stress with lipid peroxidation, which affect blood antioxidant enzyme levels and induce apoptosis of alveolar epithelial cells, are recognized as a potential mechanism leading to terminal bronchiole constriction, alveoli congestion, and exudates of erythrocyte.

In the past thirty years, the biosafety of the aboveground part of crops, including horizontal gene transferal through pollen dispersal and hybridization, has been the focus of research; however, microbial communities in the underground part are attracting increasing attention. In the present study, the soybean root-associated bacterial communities of the G2-EPSPS plus GAT transgenic soybean line Z106, its recipient variety ZH10, and Z106 treated with glyphosate (Z106J) were compared at the seedling, flowering, and seed filling stages by high-throughput sequencing of the V4 hypervariable regions of 16S rRNA gene amplicons using Illumina MiSeq. The results obtained showed no significant differences in the alpha/beta diversities of root-associated bacterial communities at the three stages among ZH10, Z106, and Z106J under field growth conditions; however, the relative abundance of four main nitrogen-fixing bacterial genera significantly differed among ZH10, Z106, and Z106J. Ternary plot results indicated that in the root compartment, the proportional contributions of rhizobial nitrogen-fixing Ensifer fredii and Bradyrhizobium elkanii, which exhibit an extremely broad nodulation host range, markedly differed among the three treatments at the three stages. Thus, the present results indicate that transgenic G2-EPSPS and GAT soybean may induce different changes in functional bacterial species in soil, such as E. fredii and B. elkanii, from ZH10, which were compensated for/enriched at the flowering and seed filling stages, respectively, to some extent through as of yet unknown mechanisms by transgenic soybean treated with glyphosate.

In the past thirty years, the biosafety of the aboveground part of crops, including horizontal gene transferal through pollen dispersal and hybridization, has been the focus of research; however, microbial communities in the underground part are attracting increasing attention. In the present study, the soybean root-associated bacterial communities of the G2-EPSPS plus GAT transgenic soybean line Z106, its recipient variety ZH10, and Z106 treated with glyphosate (Z106J) were compared at the seedling, flowering, and seed filling stages by high-throughput sequencing of the V4 hypervariable regions of 16S rRNA gene amplicons using Illumina MiSeq. The results obtained showed no significant differences in the alpha/beta diversities of root-associated bacterial communities at the three stages among ZH10, Z106, and Z106J under field growth conditions; however, the relative abundance of four main nitrogen-fixing bacterial genera significantly differed among ZH10, Z106, and Z106J. Ternary plot results indicated that in the root compartment, the proportional contributions of rhizobial nitrogen-fixing Ensifer fredii and Bradyrhizobium elkanii, which exhibit an extremely broad nodulation host range, markedly differed among the three treatments at the three stages. Thus, the present results indicate that transgenic G2-EPSPS and GAT soybean may induce different changes in functional bacterial species in soil, such as E. fredii and B. elkanii, from ZH10, which were compensated for/enriched at the flowering and seed filling stages, respectively, to some extent through as of yet unknown mechanisms by transgenic soybean treated with glyphosate.

The purpose of this study was to explore the effects of natural shikonin and its derivatives on mice experimental colitis induced by dextran sulfate sodium, and to investigate the underlying mechanisms in vivo. Our results suggested that, intragastric administration of single compound like shikonin and its derivatives contributed to attenuating symptoms of malignant induced by DSS. Meanwhile, shikonin or its derivatives could also remarkably reduce the disease activity index and histopathological scores, suppress the levels of pro-inflammatory cytokines (including IL-6, IL-1β and TNF-α), while increase that of inflammatory cytokine IL-10 in serum. Additionally, both shikonin and alkanin were found to restrain the levels of COX-2, MPO and iNOS in serum and colonic tissues. Moreover, western blotting results demonstrated that shikonin and its derivatives could inhibit the activation of the NLRP3 inflammasome and the NF-κB signaling pathway, relieve the DSS-induced disruption of colonic epithelial tight junction (TJ) in colonic tissues. Further, docking simulation had been performed to prove that shikonin and its derivatives could bind to the active sites of NLRP3 inflammasome and the NF-κB to generate an effective inflammatory effect. Taken together, our experimental data can provide some evidence for the potential use of shikonin and its derivatives to treat the inflammatory bowel disease (IBD).

Background Ulcerative colitis (UC) is one of the most challenging human diseases. Natural shikonin (SK) and its derivatives (with have higher accumulation) isolated from the root of Lithospermum erythrorhizon have numerous beneficial effects, such as wound healing and anti-inflammatory activities. Some researchers have reported that hydroxynaphthoquinone mixture (HM) and SK attenuate the acute UC induced by dextran sulfate sodium (DSS). However, no existing study has systemically investigated the effectiveness of SK and other hydroxynaphthoquinone natural derivative monomers on UC. Methods In this study, mice were treated with SK and its derivatives (25 mg/kg) and mesalazine (200 mg/kg) after DSS administration daily for one week. Disease progression was monitored daily by observing the changes in clinical signs and body weight. Results Intragastric administration natural single naphthoquinone attenuated the malignant symptoms induced by DSS. SK or its derivatives remarkably suppressed the serum levels of pro-inflammatory cytokines while increasing the inflammatory cytokine interleukin (IL)-10 . Additionally, both SK and alkanin restrained the activities of cyclooxygenase-2 (COX-2), myeloperoxidase (MPO) and inducible nitric oxide synthase (iNOS) in serum and colonic tissues. SK and its derivatives inhibited the activation of nucleotide binding oligomerization domain-like receptors (NLRP3) inflammasome and NF-κB signaling pathway, thereby relieving the DSS-induced disruption of epithelial tight junction (TJ) in colonic tissues. Conclusions Our findings shed more lights on the pharmacological efficacy of SK and its derivatives in UC against inflammation and mucosal barrier damage.

To improve the cycling performance of spinel LiMn2O4, Al-doped LiMn2O4, LiAl0.1Mn1.9O4, is synthesized using Mn1.9Al0.1O3 precursor and LiOH·H2O via a low temperature solid-phase reaction. The Mn1.9Al0.1O3 precursor, prepared from the electrolytic manganese dioxide (EMD) and Al(OH)3, is composed of spherical particles with an average diameter of 300 nm, and has a large interspace. Energy dispersive spectrometer (EDS) indicates the Al element is well distributed in Mn1.9Al0.1O3 and LiAl0.1Mn1.9O4. The scanning electron microscopy (SEM) and transmission electron microscope (TEM) images show that the LiAl0.1Mn1.9O4 sample has a high crystallinity with sizes ranging from 300 to 500 nm. Electrochemical properties of LiAl0.1Mn1.9O4 are studied by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charge-discharge. The results show that LiAl0.1Mn1.9O4 possesses better rate and cycling capabilities than LiMn2O4 at both 25 °C and 55 °C. At a rate of 5 C, the capacity retention ratio of the LiMn1.9Al0.1O4 electrode after 100 cycles is about 95% at 25 °C and about 90% at 55 °C.

Solid sphere spinel LiMn 2 O 4 materials are synthesized from porous spherical Mn 3 O 4 particles with LiOH·H 2 O via a high temperature solid-phase reaction. Porous spherical Mn 3 O 4 particles, composed of aggregated crystallites, can be obtained from as-prepared spherical β-MnOOH. The solid sphere spinel LiMn 2 O 4 particles have a high tap-density of 2.67 g·cm −3 and are well-distributed with sizes ranging from 7-9 μm. The as-prepared β-MnOOH, Mn 3 O 4 and LiMn 2 O 4 are characterized by X-ray diffraction and scanning electron microscopy. As cathode materials, solid sphere spinel LiMn 2 O 4 , exhibits excellent cycling performance and rate capability for lithium-ion batteries. The initial discharge capacities are 127.1, 118.1, 106.3 and 87 mAh·g −1 at 0.2, 1, 5 and 10 C, respectively. At 5 C the discharge capacity retention rate can be maintained at 95% after 200 cycles. Cyclic voltammetry and electrochemical impedance spectroscopy confirm the excellent electrochemical performances of the synthesized solid sphere spinel LiMn 2 O 4 materials.

We present immunogenicity data on the routine vaccination of 103 health care personnel during the 2009 H1N1 national vaccination campaign. The seroprotection rate (percentage of samples with hemagglutination inhibition titers of ≥1:40) was 83.2% at 30 days postvaccination, lower than those obtained in previously published controlled trials. Low baseline antibody levels and an increase in seroprotection in a negative-control cohort suggest that the virus remains prevalent.

Background To evaluate the risk of the recurrence and the efficiency of the vaccination, we followed-up antibody responses in patients with the 2009 pandemic H1N1 influenza and persons who received the pandemic H1N1 vaccine in Guangzhou China. Methods We collected serum samples from 129 patients and 86 vaccinated persons at day 0, 15, 30, 180 after the disease onset or the vaccination, respectively. Antibody titers in these serum samples were determined by haemagglutination inhibition (HI) assay using a local isolated virus strain A/Guangdong Liwan/SWL1538/2009(H1N1). Results HI antibody positive rate of the patients increased significantly from 0% to 60% at day 15 (χ2 = 78, P