49 research outputs found

    Vortical and Wave Modes in 3D Rotating Stratified Flows: Random Large Scale Forcing

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    Utilizing an eigenfunction decomposition, we study the growth and spectra of energy in the vortical and wave modes of a 3D rotating stratified fluid as a function of ϵ=f/N\epsilon = f/N. Working in regimes characterized by moderate Burger numbers, i.e. Bu=1/ϵ2<1Bu = 1/\epsilon^2 < 1 or Bu1Bu \ge 1, our results indicate profound change in the character of vortical and wave mode interactions with respect to Bu=1Bu = 1. As with the reference state of ϵ=1\epsilon=1, for ϵ<1\epsilon < 1 the wave mode energy saturates quite quickly and the ensuing forward cascade continues to act as an efficient means of dissipating ageostrophic energy. Further, these saturated spectra steepen as ϵ\epsilon decreases: we see a shift from k1k^{-1} to k5/3k^{-5/3} scaling for kf<k<kdk_f < k < k_d (where kfk_f and kdk_d are the forcing and dissipation scales, respectively). On the other hand, when ϵ>1\epsilon > 1 the wave mode energy never saturates and comes to dominate the total energy in the system. In fact, in a sense the wave modes behave in an asymmetric manner about ϵ=1\epsilon = 1. With regard to the vortical modes, for ϵ1\epsilon \le 1, the signatures of 3D quasigeostrophy are clearly evident. Specifically, we see a k3k^{-3} scaling for kf<k<kdk_f < k < k_d and, in accord with an inverse transfer of energy, the vortical mode energy never saturates but rather increases for all k<kfk < k_f. In contrast, for ϵ>1\epsilon > 1 and increasing, the vortical modes contain a progressively smaller fraction of the total energy indicating that the 3D quasigeostrophic subsystem plays an energetically smaller role in the overall dynamics.Comment: 18 pages, 6 figs. (abbreviated abstract

    The black hole accretion code

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    Numerical Hydrodynamics and Magnetohydrodynamics in General Relativity

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    On the Use of COBE Results

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    Expanding the industrial use of linear viscoelastic material functions

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    Polymer melts usually have relaxation times in a broad frequency range. To capture the full rheological behaviour, multiple rheometers are used. Due to the different modes of operation, combination of the data into a single rheological function often involves solving one or more inverse, ill-posed problems. Here, as an alternative approach, a new approximate direct analytical method is presented that allows the broadening of oscillatory shear data obtained from dynamic mechanical spectrometers, to low frequencies by using converted constant stress compliance data. The accuracy of the broadened curves depends on the experimental accuracy and the specific time scales of the polymer and the rheometers. The method is most effective when used in combination with inverse problem solvers. By doing so, translucence, insight, and directness from the analytic method is added to the potential accuracy of the full inverse problem solver
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