Dynamic Sealing Behavior of Sand Self-Juxtaposition Windows on a Trap-Bounding Fault in a Natural Gas Storage Site

AbstractAn understanding of across-fault seals is essential for planning an injection/production strategy for a fault-bounded gas storage site. In addition, it is more likely to permit lateral leakage for a fault with sand self-juxtaposition windows. This paper is aimed at identifying the dynamic sealing behaviors of a sand self-juxtaposition fault on the geological and gas injection timescales. Banzhongbei gas storage site, China, was taken as a target area, and fault seals and hydrocarbon distributions within the original reservoirs were studied. The results showed that across-fault pressure differences of 0.085~0.146 MPa (equivalent to 41.6~71.5 m oil-column and 27.0~46.4 m gas-column heights) were supported by sand self-juxtaposition windows on the B816 fault, and the resultant absolute permeability (5.97×10−2~5.69×10−1 mD) of the fault was nearly 3~4 orders of magnitude lower than the average absolute permeability of reservoirs (1.16×102 mD). Gas composition contrasts, between the original and injection gas coupled with dynamic pressure monitoring data, indicated that lateral leakage occurred across sand self-juxtaposition windows under the condition of high across-fault pressure difference. However, the low-permeability fault showed strong negative influence on the efficiency of fluid flow in the model calculations and prolongs the timescales of pressure-difference decayed as much as 5 orders of magnitude relative to those of nonfault model calculations. These modeled dynamic sealing behaviors of sand self-juxtaposition windows may lead to a better understanding of the relative retardation of across-fault gas flow by weak sealing faults on the gas injection/production timescale

First identification of canine adenovirus 1 in mink and bioinformatics analysis of its 100 K protein

IntroductionAnimal trade favors the spreading of emerging canine adenovirus 1 (CAdV-1) in mink. Because the 100K protein is not exposed to the viral surface at any stage, it can be used to differentiate the vaccine from wild virus infection. However, no related research has been conducted. This study aimed to find evidence of CAdV-1 in mink and predict the character of the 100K protein in the current circulating CAdV-1 strain of mink.MethodIn this experiment, the identification of CAdV-1, the phylogenetic tree, homology, and bioinformatics analysis of 100K were conducted.ResultsThe results showed that the CAdV-1 was identified in the mink and that its Fiber was located in a separate branch. It was closely related to strains isolated from Norwegian Arctic fox and Red fox. 100K was located in a separate branch, which had the closest genetic relationship with skunks, porcupines, raccoons, and hedgehogs and a far genetic relationship with the strains in dogs. 100K protein is an unstable and hydrophobic protein. It had evidence of selective pressure and recombination, 1 glycosylation site, 48 phosphorylation sites, 60 dominant B cell epitopes, and 9 peptides of MHC-I and MHC-II. Its subcellular localization was mainly in the endoplasmic reticulum and mitochondria. The binding sites of 100K proteins were DBP proteins and 33K proteins.DiscussionThe stains in the mink were different from fox. The exploration of its genomic characteristics will provide us with a deeper understanding of the prevention of canine adenovirus

Correlation analysis of aqueous humor metabolomics with myopic axial length and choroidal parameters

Abstract Background To explore differential metabolites in the aqueous humor of patients with different axial lengths and their correlations with axial length and choroidal parameters. Methods In this study, we included 12 patients with axial lengths less than 24 mm, 11 patients with axial lengths between 24 and 26 mm, and 11 patients with axial lengths greater than 26 mm. We collected their aqueous humor samples during cataract surgery for liquid chromatography-mass spectrometry metabolomic analysis. Simultaneously, we collected relevant clinical parameters such as axial length, subfoveal choroidal thickness, and choroidal vascular index. Correlations between clinical data, differential metabolites, and clinical indicators were analyzed. In addition, we plotted receiver operating characteristic curves. Results The results showed that axial length was significantly negatively correlated with choroidal thickness (r=-0.7446, P < 0.0001), and that several differential metabolites were significantly correlated with certain clinical parameters. After analyzing receiver operating characteristic curves, 5-methoxytryptophol and cerulenin were found to have excellent discriminative power, demonstrating their potential as biomarkers. In the enrichment analysis, we found that the differential metabolites among each group were involved in several special pathways (Taurine and Hypotaurine Metabolism, Vitamin B6 Metabolism, Pantothenate, and coenzyme A Biosynthesis), suggesting that abnormalities in these metabolic pathways may play a role in the process of axial myopia. Conclusions Our study identified alterations in certain metabolic pathways in different axial lengths. At the same time, we found several metabolites with significant correlation with clinical indicators, among which 5-methoxytryptophol and cerulenin were associated with axial myopia. Clinical trial registration Registration date:11/04/2022. Trial registration number: ChiCTR2200058575. Trial registry: The First Affiliated Hospital of the Zhejiang University School of Medicine