26 research outputs found

    Mathematical Model of Oxygen Labeling to Study Heart Energy Transfer

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    Effect of Target Thickness on Cratering and Penetration of Projectiles Impacting at Velocities to 13,000 Feet Per Second

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    In order to determine the effects of target thickness on the penetration and cratering of a target resulting from impacts by high-velocity projectiles, a series of experimental tests have been run. The projectile-target material combinations investigated were aluminum projectiles impacting aluminum targets and steel projectiles impacting aluminum and copper targets. The velocity spectrum ranged from 4,000 ft/sec to 13,000 ft/sec. It has been found that the penetration is a function of target thickness provided that the penetration is greater than 20 percent of the target thickness. Targets of a thickness such that the penetration amounts to less than 20 percent of the thickness may be regarded as quasi-infinite. An empirical formula has been established relating the penetration to the target thickness and to the penetration of a projectile of the same mass, configuration, and velocity into a quasi- infinite target. In particular, it has been found that a projectile can completely penetrate a target whose thickness is approximately one and one-half times as great as the penetration of a similar projectile into a quasi-infinite target. The diameter of a crater has also been found to be a function of the target thickness provided that the target thickness is not greater than the projectile length in the case of cylindrical projectiles and not greater than two to three times the projectile diameter in the case of spherical projectiles

    Symbolic flux analysis for genome-scale metabolic networks

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    BACKGROUND: With the advent of genomic technology, the size of metabolic networks that are subject to analysis is growing. A common task when analyzing metabolic networks is to find all possible steady state regimes. There are several technical issues that have to be addressed when analyzing large metabolic networks including accumulation of numerical errors and presentation of the solution to the researcher. One way to resolve those technical issues is to analyze the network using symbolic methods. The aim of this paper is to develop a routine that symbolically finds the steady state solutions of large metabolic networks. RESULTS: A symbolic Gauss-Jordan elimination routine was developed for analyzing large metabolic networks. This routine was tested by finding the steady state solutions for a number of curated stoichiometric matrices with the largest having about 4000 reactions. The routine was able to find the solution with a computational time similar to the time used by a numerical singular value decomposition routine. As an advantage of symbolic solution, a set of independent fluxes can be suggested by the researcher leading to the formation of a desired flux basis describing the steady state solution of the network. These independent fluxes can be constrained using experimental data. We demonstrate the application of constraints by calculating a flux distribution for the central metabolic and amino acid biosynthesis pathways of yeast. CONCLUSIONS: We were able to find symbolic solutions for the steady state flux distribution of large metabolic networks. The ability to choose a flux basis was found to be useful in the constraint process and provides a strong argument for using symbolic Gauss-Jordan elimination in place of singular value decomposition

    A Fortran to C Converter

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    We describe f 2c, a program that translates Fortran 77 into C or C++. F2c lets one portably mix C and Fortran and makes a large body of well-tested Fortran source code available to C environments
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