Determination of Klinkenberg Permeability Conditioned to Pore-Throat Structures in Tight Formations

This paper has developed a pragmatic technique to efficiently and accurately determine the Klinkenberg permeability for tight formations with different pore-throat structures. Firstly, the authors use steady-state experiments to measure the Klinkenberg permeability of 56 tight core samples under different mean pore pressures and confining pressures. Secondly, pressure-controlled mercury injection (PMI) experiments and thin-section analyses are conducted to differentiate pore-throat structures. After considering capillary pressure curve, pore types, throat size, particle composition, and grain size, the pore-throat structure in the target tight formation was classified into three types: a good sorting and micro-fine throat (GSMFT) type, a moderate sorting and micro-fine throat (MSMFT) type, and a bad sorting and micro throat (BSMT) type. This study found that a linear relationship exists between the Klinkenberg permeability and measured gas permeability for all three types of pore-throat structures. Subsequently, three empirical equations are proposed, based on 50 core samples of data, to estimate the Klinkenberg permeability by using the measured gas permeability and mean pore pressure for each type of pore-throat structure. In addition, the proposed empirical equations can generate accurate estimates of the Klinkenberg permeability with a relative error of less than 5% in comparison to its measured value. The application of the proposed empirical equations to the remaining six core samples has demonstrated that it is necessary to use an appropriate equation to determine the Klinkenberg permeability of a specific type of pore-throat structure. Consequently, the newly developed technique is proven to be qualified for accurately determining the Klinkenberg permeability of tight formations in a timely manner

Melatonin mediates monochromatic green light-induced satellite cell proliferation and muscle growth in chick embryo.

BackgroundGreen light penetrates the skull and has directly affected on the secretion of melatonin in plasma, which regulates the endocrine activities to influence the muscle growth, satellite cell mitotic activity and quality properties of meat from the embryonic period to posthatch in chick. Pituitary adenylate cyclase-activating polypeptide 6-38 (PACAP6-38) could inhibit the synthesis and secretion of pineal melatonin. Finding a new way for exploring the mechanism of light-regulated muscle growth in ovo is essential for promoting the productive performance in poultry.MethodsChick embryos were exposed to darkness (D-group) and green light (G-group) throughout the embryonic period, and injected with PACAP6-38 or saline at embryonic day 8. Plasma hormone, skeletal muscle fiber areas, satellite cell proliferation activity, paired domain homeobox transcription factor 7 and myogenic regulatory factors were observed.ResultsBy saline treatment, the percentage of proliferating cell nuclear antigen immunoreactive cells and mitotic activity of satellite cells in skeletal muscle were higher in G-group than those of in D-group at post-hatching day 0. With the increase of plasma melatonin, green light promoted the secretion of growth hormone (GH) and insulin like factor 1 (IGF-1) in plasma, the satellite cell proliferation, the size of muscle fiber, as well as the mRNA expressions of Pax7, myogenic regulatory factors and IGF-1R. After PACAP6-38 treatment to inhibit the secretion of melatonin in ovo, aforementioned parameters were remarkably decreased and the difference of these parameters was disappeared between D-group and G-group.ConclusionThese data indicated that stimulation with monochromatic green light during incubation enhanced the secretion of melatonin and up-regulation of GH-IGF-1 axis to activate the satellite cells proliferation and myofiber formation, involving the expression of Pax7 and myogenic regulatory factors

Motion Synchronous Composite Decoupling with Fewer Sensors on Multichannel Hydraulic Force Control for Aircraft Structural Loading Test System

The aircraft full-scale fatigue test is widely used in the modern aircraft industry for the safety of flight. Generally, the aircraft full-scale fatigue test is achieved by structural loading; multiple hydraulic actuators are used to apply load for force control. The fatigue loading test takes approximately several years. A key challenge is how to accelerate the loading frequency to shorten the total test time. Nevertheless, when pluralities of hydraulic actuator simultaneously increase the loading frequency, the mutual coupling force from the low rigidity of the aircraft structure will cause a large loading error, meaning that the test cannot be implemented. Although it is possible to reduce error by adding sensors, the force sensors need to connect several kilometers of cable. This paper proposed a novel motion synchronous composite decoupling control strategy with fewer sensors. The control method compensates the negative coupling effect of the channels by integrating the command signals and feedback signals of all channels. It can suppress coupling force and reduce errors at higher frequencies, thereby shortening the experiment time. Opposed to traditional decoupling control methods, advantages of this strategy are that it only needs force sensors and it does not need additional displacement or velocity and acceleration sensors to collect state variables for building the state space. Furthermore, it has been experimentally verified that the new motion synchronous composite decoupling control method can indeed guarantee sufficient control accuracy when the test frequency is increased. The method has great economic significance for shortening test duration

The immunologic and antioxidant effects of L-phenylalanine on the uterine implantation of mice embryos during early pregnancy

L-phenylalanine (L-PHE) is a synthetic precursor of catecholamines. Because it cannot be synthesised by an organism, it must be absorbed from the environment. Despite the wide use of L-PHE, whether L-PHE has a negative impact on embryo implantation and development is poorly understood. This study attempted to determine the roles of L-PHE in embryo implantation and development and in the immune response and antioxidant status of the uterus in early pregnancy mice injected intraperitoneally with 320 mg/kg L-PHE. The embryo number of treated mice decreased by 57.6%, and the size of their embryos was reduced by 2.8% (P>0.05) along the long diameter and 11.9% (P<0.05) along the short diameter at E9 compared with control mice. In addition, L-PHE significantly suppressed B lymphocyte proliferation. L-PHE increased IL-2 secretion but decreased the IL-4 concentration, thereby up-regulating the ratio of IL-2/IL-4 to 1.37-8.45. An analysis of the oxidant and antioxidant status showed that, compared with the control mice, the level of superoxide dismutase activity decreased by 21.54%- 39.94% and the glutathione peroxidase activity decreased by 15.27%-18.96% among the L-PHE-treated mice at E1-E9. However, the malonaldehyde content increased by 14.29%-90.11% among the L-PHE-treated mice. Therefore, L-PHE impaired embryo implantation by disrupting cytokine-based immunity and oxidative stress in the uterus