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Anomalous Scaling

So far we have discussed random walks with a finite mean waiting time and a finite variance of the jump length. These models lead to the classical parabolic scaling X x/e, t t/e. The governing macroscopic equation for the density p becomes the standard diffusion equation. Let us now consider two cases for which the scaling is anomalous and the mean-field equations for p are fractional diffusion equations. [Pg.94]

1 Finite Mean Waiting Time and Infinite Variance [Pg.94]

Suppose that the jump PDF w(z) is an even function and decreases as [Pg.94]

From a probabilistic point of view, S (t) is the attractor for the rescaled particle position X (t). To understand this, consider first a discrete random walk. The rescaled position of a particle with jumps Z that are symmetric with respect to zero is Y = / J2 i=i with 0 a 2. We are interested in the limit n oo, such that the sequence T converges toward a new random variable Z in distribution, [Pg.95]

Recall that, in general, the stable random variable Z involves four parameters the exponent (stable index) 0 a 2, the skewness —1 1, the shift a e K, [Pg.95]


If the concentration field had exactly the same local Holder exponent (a) everywhere in space, the spatial averaging would be irrelevant and the scaling exponents would be given by (q = qa. This is a valid approximation for small q, but typically there are corrections that lead to an anomalous scaling when the fluctuations of the finitetime Lyapunov exponents is taken into account. As time increases... [Pg.181]

Abraham and Bowen (2002) applied the above theoretical description to an analysis of ocean data from satellite observations (Fig. 6.6) and showed that the distribution of sea-surface temperature modelled as a relaxation to the atmospheric temperature is consistent with the anomalous scaling exponents given by (6.43). [Pg.183]

Figure 6.6 Anomalous scaling exponents of sea-surface temperature from Abraham and Bowen (2002). The solid stars are the exponents obtained from satellite data and the other symbols represent scaling exponents calculated from simulating the sea-surface temperature as a linear relaxation with different relaxation rates. Figure 6.6 Anomalous scaling exponents of sea-surface temperature from Abraham and Bowen (2002). The solid stars are the exponents obtained from satellite data and the other symbols represent scaling exponents calculated from simulating the sea-surface temperature as a linear relaxation with different relaxation rates.
Huo S, Schwarzacher W. (2001) Anomalous scaling of the surface width during Cu electrodeposition. Phys Rev Lett 86 256-259. [Pg.342]

In many cases dispersive-looking transients cannot be identified with anomalous scaling. The latter is believed to be a direct consequence of the... [Pg.302]

The parameters were then further refined by four successive least-squares procedures, as described by Hughes (1941). Only hk() data were used. The form factor for zinc was taken to be 2-4 times the average of the form factors for magnesium and aluminum. The values of the form factor for zinc used in making the average was corrected for the anomalous dispersion expected for copper Kot radiation. The customary Lorentz, polarization, temperature, and absorption factors were used. A preliminary combined scale, temperature, and absorption factor was evaluated graph-... [Pg.607]

However, many anomalous results have been reported for these substrates. The benzylic position is not always the most favored. One thing certain is that aromatic hydrogens are seldom abstracted if there are aliphatic ones to compete (note from Table 5.3, that D for Ph—H is higher than that for any alkyl H bond). Several a- scales (similar to the a, ct, and scales discussed in Chapter 9) have been developed for benzylic radicals. ... [Pg.902]

Figure 6.5. 5 0 of tooth enamel phosphate versus body size (log scale) for Kenyan fauna analyzed in this study. With the exception of the dikdik, there is a general association between the two variables. In contrast to tbe body-size model (Bryant and Froelicb 1995) wbicb predicts a range of values close to l%o, however, the measured range in 8 0 values for species averages is 5%a. This and the anomalous values for the dikdik reflect physiological and behavioral adaptations by these desert adapted species. [Pg.130]

It is to be noted in Table XXII that o (a) = ( (p) ( -03) only for the halogens, CeHs.SiMes, NO2, and MeCO. It is evident that the aj (p) values are appreciably more positive than the corresponding ct (a) for all the other —R substituents (NMea, NHj, OMe, SMe, and Me). Where differences exist between these two scales for +R substituents, cr p) parameters are less positive, however. A clearly anomalous result is the sequence of -a (p) values NHj, NMej < OMe < F. [Pg.51]

To complete the discussion of the second-order interaction between tunneling centers, we note that the corresponding contribution to the heat capacity in the leading low T term comes from the ripplon-TLS term and scales as 7 +2 where a is the anomalous exponent of the specific law. Within the approximation adopted in this section, a = 0. However, it is easily seen that the magnitude of the interaction-induced specific heat is down from the two-level system value by a factor of 10(a/ ) ([Pg.188]

Time intervals permitting displacement values in the scaling window a< )tortuous flow as a result of random positions of the obstacles in the percolation model [4]. Hydrodynamic dispersion then becomes effective. For random percolation clusters, an anomalous, i.e., time dependent dispersion coefficient is expected according to... [Pg.220]

Membrane-integrated proteins were always hard to express in cell-based systems in sufficient quantity for structural analysis. In cell-free systems, they can be produced on a milligrams per milliliter scale, which, combined with labeling with stable isotopes, is also very amenable forNMR spectroscopy [157-161]. Possible applications of in vitro expression systems also include incorporation of selenomethionine (Se-Met) into proteins for multiwavelength anomalous diffraction phasing of protein crystal structures [162], Se-Met-containing proteins are usually toxic for cellular systems [163]. Consequently, rational design of more efficient biocatalysts is facilitated by quick access to structural information about the enzyme. [Pg.52]

But one can ask the question why normal muonium is observed at all if the global energy minimum (i.e., the stable site) is really at the bond center (anomalous muonium). On the time scale of the muon lifetime, relaxations of the Si atoms may be sufficiently slow to effectively trap the muon in the low-density regions of the crystal, where relaxation of the host atoms is... [Pg.632]

It is more difficult to interpret micellar effects upon reactions of azide ion. The behavior is normal , in the sense that k /kw 1, for deacylation, an Sn2 reaction, and addition to a carbocation (Table 4) (Cuenca, 1985). But the micellar reaction is much faster for nucleophilic aromatic substitution. Values of k /kw depend upon the substrate and are slightly larger when both N 3 and an inert counterion are present, but the trends are the same. We have no explanation for these results, although there seems to be a relation between the anomalous behavior of the azide ion in micellar reactions of aromatic substrates and its nucleophilicity in water and similar polar, hydroxylic solvents. Azide is a very powerful nucleophile towards carboca-tions, based on Ritchie s N+ scale, but in water it is much less reactive towards 2,4-dinitrohalobenzenes than predicted, whereas the reactivity of other nucleophiles fits the N+ scale (Ritchie and Sawada, 1977). Therefore the large values of k /kw may reflect the fact that azide ion is unusually unreactive in aromatic nucleophilic substitution in water, rather than that it is abnormally reactive in micelles. [Pg.256]

Thus, the model predicts that thermal fluctuations in the tilt and curvature change the way that the tubule radius scales with chiral elastic constant— instead of r oc (THp) 1, the scaling has an anomalous, temperature-dependent exponent. This anomalous exponent might be detectable in the scaling of tubule radius as a function of enantiomeric excess in a mixture of enantiomers or as a function of chiral fraction in a chiral-achiral mixture. [Pg.354]


See other pages where Anomalous Scaling is mentioned: [Pg.173]    [Pg.404]    [Pg.476]    [Pg.487]    [Pg.15]    [Pg.84]    [Pg.183]    [Pg.241]    [Pg.2]    [Pg.94]    [Pg.94]    [Pg.99]    [Pg.197]    [Pg.333]    [Pg.333]    [Pg.173]    [Pg.404]    [Pg.476]    [Pg.487]    [Pg.15]    [Pg.84]    [Pg.183]    [Pg.241]    [Pg.2]    [Pg.94]    [Pg.94]    [Pg.99]    [Pg.197]    [Pg.333]    [Pg.333]    [Pg.486]    [Pg.429]    [Pg.489]    [Pg.576]    [Pg.194]    [Pg.112]    [Pg.614]    [Pg.619]    [Pg.93]    [Pg.525]    [Pg.658]    [Pg.472]    [Pg.524]    [Pg.345]    [Pg.346]    [Pg.43]    [Pg.67]    [Pg.241]    [Pg.350]   


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