Prediction of soil available phosphorus based on soil organic carbon

There are many cases in which it is desirable to determine relationships among some soil physical and chemical properties. In soil studies, soil available phosphorous (AP) are often determined using laboratory tests, but it may be more suitable and economical to develop a pedotransfer function which uses some easily available soil properties. In this study, a pedotransfer function for predicting soil AP from soil organic carbon(OC) was suggested and soil AP was estimated as a function of soil OC. The soil AP predicted from the soil AP pedotransfer function was compared to the soil AP determined by laboratory test using the paired samples test and the Bland-Altman approach. The soil AP predicted by the soil AP pedotransfer function was not significantly different from the soil AP determined by laboratory test (P>0.05). The mean difference between the soil AP pedotransfer function and laboratory test was 1.57 ppm (95% confidence interval: -2.88 and 6.03 ppm; P = 0.453). The standard deviation of the soil AP differences was 7.01 ppm. The statistical results of the study indicated that the soil AP pedotransfer function provides an easy, economic and brief methodology to estimate soil AP and in order to predict soil AP based on soil OC the pedotransfer function AP = 0.7927 e 4.9922 OC with R2 = 0.92 can be recommended

Interference fracturing: Nonuniform distributions of perforation clusters that promote simultaneous growth of multiple hydraulic fractures

One of the important hurdles in horizontal-well stimulation is the generation of hydraulic fractures (HFs) from all perforation clusters within a given stage, despite the challenges posed by stress shadowing and reservoir variability. In this paper, we use a newly developed, fully coupled, parallel-planar 3D HF model to investigate the potential to minimize the negative impact of stress shadowing and thereby to promote more-uniform fracture growth across an array of HFs by adjusting the location of the perforation clusters. In this model, the HFs are assumed to evolve in an array of parallel planes with full 3D stress coupling while the constant fluid influx into the wellbore is dynamically partitioned to each fracture so that the wellbore pressure is the same throughout the array. The model confirms the phenomenon of inner-fracture suppression because of stress shadowing when the perforation clusters are uniformly distributed. Indeed, the localization of the fracture growth to the outer fractures is so dominant that the total fractured area generated by uniform arrays is largely independent of the number of perforation clusters. However, numerical experiments indicate that certain nonuniform cluster spacings promote a profound improvement in the even development of fracture growth. Identifying this effect relies on this new model's ability to capture the full hydrodynamical coupling between the simultaneously evolving HFs in their transition from radial to Perkins-Kern-Nordgren (PKN)-like geometries (Perkins and Kern 1961; Nordgren 1972)

Effects of aminoperimidine on electrolyte transport across amphibian skin

The effect of aminoperimidine (AP)on transepithelial Na+ transport and Cl- conductance (G(Cl)) of isolated amphibian skin (Bufo viridis and Rana esculenta) was analyzed using transepithelial and intracellular electrophysiological techniques. AP, applied at concentrations between 30 and 100 mu M from the mucosal side, stimulated Na+ transport rapidly and reversibly by more than 30% of the control value due to an increase in apical membrane Na+ permeability. Influence of AP on basolateral membrane conductance and effective driving force for Na+ were negligible. Voltage-activated G(Cl) of toad skin, but not the resting, deactivated conductance, as well as spontaneously high G(Cl) in frog skin was rapidly inhibited by AP in a concentration-dependent manner. The half-maximal inhibitory concentration of 20 mu M is the highest hithero reported inhibitory power for G(Cl) in amphibian skin. The effect of AP on G(Cl) was slowly and incompletely reversible even after brief exposure to the agent. Serosal application of AP had similar, albeit delayed effects on both Nai and Cl- transport. AP did not interfere with the Cl- pathway after it was opened by 100-300 mu M CPT-cAMP, a membrane-permeable, nonhydrolyzed analogue of cAMP. Inhibition of the voltage-activated G(Cl) by AP was attenuated or missing when AP was applied during voltage perturbation to serosa-positive potentials. Since AP is positively charged at physiological pH, it suggests that the affected site is located inside the Cl- pathway at a certain distance from the external surface. AP affects then the Na+ and Cl- transport pathways independent of each other. The nature of chemical interference with AP, which is responsible for the influence on the transport of Na+ and Cl-, remains to be elucidated

Macrophage autophagy in atherosclerosis

Macrophages play crucial roles in atherosclerotic immune responses. Recent investigation into macrophage autophagy (AP) in atherosclerosis has demonstrated a novel pathway through which these cells contribute to vascular inflammation. AP is a cellular catabolic process involving the delivery of cytoplasmic contents to the lysosomal machinery for ultimate degradation and recycling. Basal levels of macrophage AP play an essential role in atheroprotection during early atherosclerosis. However, AP becomes dysfunctional in the more advanced stages of the pathology and its deficiency promotes vascular inflammation, oxidative stress, and plaque necrosis. In this paper, we will discuss the role of macrophages and AP in atherosclerosis and the emerging evidence demonstrating the contribution of macrophage AP to vascular pathology. Finally, we will discuss how AP could be targeted for therapeutic utility

A Comparative Study of an Asymptotic Preserving Scheme and Unified Gas-kinetic Scheme in Continuum Flow Limit

Asymptotic preserving (AP) schemes are targeting to simulate both continuum and rarefied flows. Many AP schemes have been developed and are capable of capturing the Euler limit in the continuum regime. However, to get accurate Navier-Stokes solutions is still challenging for many AP schemes. In order to distinguish the numerical effects of different AP schemes on the simulation results in the continuum flow limit, an implicit-explicit (IMEX) AP scheme and the unified gas kinetic scheme (UGKS) based on Bhatnagar-Gross-Krook (BGk) kinetic equation will be applied in the flow simulation in both transition and continuum flow regimes. As a benchmark test case, the lid-driven cavity flow is used for the comparison of these two AP schemes. The numerical results show that the UGKS captures the viscous solution accurately. The velocity profiles are very close to the classical benchmark solutions. However, the IMEX AP scheme seems have difficulty to get these solutions. Based on the analysis and the numerical experiments, it is realized that the dissipation of AP schemes in continuum limit is closely related to the numerical treatment of collision and transport of the kinetic equation. Numerically it becomes necessary to couple the convection and collision terms in both flux evaluation at a cell interface and the collision source term treatment inside each control volume

Dinucleoside polyphosphates : newly detected uraemic compounds with an impact on leucocyte oxidative burst

Background. Dinucleoside polyphosphates (NpnN) have pathophysiologic roles in cardiovascular disease and are newly detected uraemic retention solutes. They were retrieved in human plasma, tissues and cells. Although their impact on several cell systems involved in vascular damage (endothelium, smooth muscle cells and thrombocytes) has been evaluated, their effect on different types of leucocytes has never been studied. Methods. This study evaluates, for the first time, the impact of NpnN on monocyte, granulocyte and lymphocyte oxidative burst activity at baseline and after stimulation with N-formyl-methionine-leucine-phenylalanine (fMLP) and phorbol 12-myristate 13-acetate (PMA) in whole blood. Diadenosine triphosphate (Ap(3)A) to diadenosine hexaphosphate (Ap(6)A) were tested to investigate the effect of the number of phosphate groups on reactive oxygen species (ROS) production. The effect of the type of nucleoside was evaluated by comparing adenosine guanosine tetraphosphate, diguanosine tetraphosphate, uridine adenosine tetraphosphate (Up(4)A) and diadenosine tetraphosphate (Ap(4)A). Results. This study demonstrated that lymphocytes are especially susceptible to intracellular diadenosine polyphosphates. Depending on the phosphate chain length, different effects were observed. At baseline and with fMLP Ap(4)A, Ap(5)A and Ap(6)A enhanced lymphocyted-free radical production. In addition, Ap(3)A, Ap(4)A and Ap5A increased PMA-stimulated ROS production in lymphocytes. Monocytes and granulocytes parallel the lymphocyte response albeit with an inhibition of Ap(6)A on granulocytes. Considering NpnN with four phosphate groups, Up(4)A showed the most important stimulatory effects on monocytes and Ap(4)A on lymphocytes. Conclusions. NpnN mainly have a leucocyte-activating impact, most significant for Ap(4)A, considering phosphate chain length, and for Up(4)A, considering the type of nucleosides. These results suggest that the pro-inflammatory effects of NpnN can contribute to the development of atherosclerosis, probably in the early stages of chronic kidney disease, but their chemical composition affects their activity

Polynomial manipulator AP-168

Linear Systems Design Evaluation Program, AP-168 combines the many different analysis techniques used to evaluate and manipulate polynomials. The single program is a pseudo instruction abstraction. It allows the user to enter polynomials of the laplace operators and to manipulate them freely