1,217 research outputs found

    Shikimate pathway in apicomplexan parasites

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    Dynamic response simulation through system identification.

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    Nonlinear dynamic systems, such as those associated with structural testing of vehicles, are considered. The vehicle, or a substructure, is mounted in a test rig that is normally driven by servo-hydraulic actuators. The specimen and test rig form a nonlinear dynamic system. These test systems assure the durability of vehicles by reproducing a structural response time history that has been measured in a road test of a vehicle. For this, a force or displacement input to the actuators’ control system must be determined as a function of time.Current practice employs an iterative algorithm, using a frequency response function to represent the system. The conventional iteration is a particular version of well established numerical techniques for solving nonlinear systems. However, the success of the iteration is dependent on the degree of nonlinearity and on the level of noise in the signals coming from the system.This paper advocates identifying the system to improve its representation in the iterative algorithm. The theory underpinning the alternative algorithm is presented and a comparison is made between the performances of the two algorithms, using computer simulations based on Duffing's equation. These simulations show that, even for this simple model, the alternative algorithm is faster, more reliable and more tolerant of response noise

    Dynamic response simulation for a nonlinear system.

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    Laboratory simulation testing has for many years contributed significantly to the durability and quality of motor vehicles. Most sophisticated test rigs use an iterative algorithm that generates the input drive files that reproduce service environments under laboratory conditions. Essentially the algorithm solves a nonlinear, multiple channel dynamic system. In this paper, the nonlinear problem is recast as a system of algebraic equations. This mathematical framework allows the application of alternative but well understood solution techniques. Using mathematical simulations, conclusions are drawn concerning the choice of iteration gain in the current algorithm and the better performance of alternative numerical solution procedures

    The screen representation of vector coupling coefficients or Wigner 3j symbols: exact computation and illustration of the asymptotic behavior

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    The Wigner 3j3j symbols of the quantum angular momentum theory are related to the vector coupling or Clebsch-Gordan coefficients and to the Hahn and dual Hahn polynomials of the discrete orthogonal hyperspherical family, of use in discretization approximations. We point out the important role of the Regge symmetries for defining the screen where images of the coefficients are projected, and for discussing their asymptotic properties and semiclassical behavior. Recursion relationships are formulated as eigenvalue equations, and exploited both for computational purposes and for physical interpretations.Comment: 14 pages, 8 figures, presented at ICCSA 2014, 14th International Conference on Computational Science and Application

    On the sense of taste in two Malagasy Primates (Microcebus murinus and Eulemur mongoz)

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    The relationship between phylogeny and taste is of growing interest. In this study we present recordings from the chorda tympani proper (CT) nerve of two lemuriforme primates, the lesser mouse lemur (Microcebus murinus) and the mongoose lemur (Eulemur mongoz), to an array of taste stimuli which included the sweeteners acesulfame-K, alitame, aspartame, D-glucose, dulcin, monellin, neohesperidin dihydrochalcone (NHDHC), saccharin, sodium superaspartame, stevioside, sucralose (TGS), sucrose, suosan, thaumatin and xylitol, as well as the non-sweet stimuli NaC1, citric acid, tannin and quinine hydrochloride. In M.murinus the effects of the taste modifiers gymnemic acid and miraculin on the CT response were recorded. Conditioned taste aversion (CTA) experiments in M.murinus and two-bottle preference (TBP) tests in E.mongoz were also conducted. We found that all of the above tastants except thaumatin elicited a CT response in both species. The CTA technique showed that M.murinus generalized from sucrose to monellin but not to thaumatin. The intake of aspartame, ranging in concentration from 0.1 to 30 mM was measured in E.mongoz with TBP tests. At no concentration did we see a preference, but there was a significant rejection of 10 and 30 mM aspartame (P←0.025). Miraculin had no effects on the CT response to acids, and gymnemic acid did not selectively suppress the CT response to sucrose or that of any other sweeteners. The absence of ability to taste thaumatin in these species supports the dichotomy between catarrhine and non-catarrhine species. The difference in results with thaumatin and monellin indicate that their sweet moieties are not identical. It also points to a phylogenetic difference in taste within the prosimian group. Further, the results with aspartame indicate that the perception of sweetness from aspartame is limited to catarrhine species. Finally, neither miraculin nor gymnemic acid exhibit the same taste modifying effects in lemuriformes as they do in hominoidea. Thus the results with gymnemic acid and miraculin corroborate those obtained earlier in other prosimian

    Valence-quark distributions in the pion

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    We calculate the pion's valence-quark momentum-fraction probability distribution using a Dyson-Schwinger equation model. Valence-quarks with an active mass of 0.30 GeV carry 71% of the pion's momentum at a resolving scale q_0=0.54 GeV = 1/(0.37 fm). The shape of the calculated distribution is characteristic of a strongly bound system and, evolved from q_0 to q=2 GeV, it yields first, second and third moments in agreement with lattice and phenomenological estimates, and valence-quarks carrying 49% of the pion's momentum. However, pointwise there is a discrepancy between our calculated distribution and that hitherto inferred from parametrisations of extant pion-nucleon Drell-Yan data.Comment: 8 pages, 3 figures, REVTEX, aps.sty, epsfig.sty, minor corrections, version to appear in PR
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