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Being nonGaussian, one of the obstacles at this stage for using these kinds of stable superposition processes in the context of modeling data traf c is that their statistical parameters (which speci es the marginals) and H (Eq (205)) do not de ne them completely; there exist a number of different dependent, stationary increment processes with stable marginals with the same and same self-similarity parameter H see, for example, Samorodnitsky and Taqqu [33] This is in stark contrast to FGN, where knowing the second-order statistical characteristics (ie, variance and Hurst parameter H) uniquely de nes the process, due to Gaussianity 203 THE SMALL-TIME SCALING BEHAVIOR OF NETWORK TRAFFIC The analysis of measured network traf c and resulting understanding of some of its underlying structure outlined in Section 20.

Case 2 (i > K + B p G 1): In this case, the way to estimate Bi depends on whether or not frame i has arrived before all the data in the client buffer is consumed as illustrated in Figure 8.3. If (Ti 1 + Bi 1 ) Ti 0, that means frame i has arrived before the client buffer becomes empty, then Bi is estimated as: Bi = (Bi 1 + Ti 1 ) Ti + 1/G (8.4)

2 have led to the realization that while wide-area traf c is consistent with asymptotic self-similarity or large-time scaling behavior, its small-time scaling features are very different from those observed over large time scales Thus, to provide an adequate and more complete description of.

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facilitate the cleavage of C C C and other bonds by water. Lyases cat C, O, N alyze the cleavage of these same bonds by elimination, leaving double bonds (or, in the reverse mode, catalyze the addition of groups across double bonds). Isomerases facilitate geometric or structural rearrangements or isomerizations. Finally, ligases catalyze the joining of two molecules, and often require the hydrolysis of a pyrophosphate bond in the cofactor adenosine triphosphate (ATP, Fig. 2.4) to provide the energy required for the synthetic step. The enzymes D-amino acid oxidase and lactate dehydrogenase (Eqs. 2.2 and 2.6) have the numbers E.C. 1.4.3.3 and E.C. 1.1.1.28, respectively; both are oxidoreductases, and therefore fall into the rst of the six main divisions. The enzyme cholesterol esterase catalyzes the hydrolysis of cholesterol esters into cholesterol and free fatty acids (Eq. 2.7), and has been assigned E.C. 3.1.1.13.

Otherwise, if (Ti 1 + Bi 1 ) Ti 0, that means the client buffer has been empty for a period of time before frame i arrived, then Bi is simply equal to the time value of a frame, i.e.: Bi = 1/G (8.5)

actual network traf c, it is necessary to deal with these small-time scaling features and to ultimately understand their cause and effects. To this end, we summarize in this section our current understanding of this very recent development in network traf c analysis and modeling by introducing concepts that are novel to the networking area, for example, multifractals, conservative cascades, and multiplicative structure, and illustrate their relevance to networking. 20.3.1 Multifractals

From a networking perspective, it comes as no surprise that protocol-speci c mechanisms and end-to-end congestion control algorithms operating on small time scales and at the different layers in the hierarchical structure of modern data networks give rise to structural properties that are drastically different from the largetime scaling behavior, which has been shown earlier to be mainly due to global user and=or session characteristics Since these networking mechanisms determine largely the actual ow of packets across the networks, they are likely to cause the traf c to exhibit pronounced local variations and irregularities which, per se, cannot be expected to have any obvious connection to the self-similar behavior of the traf c over large time scales.

2:7 In addition to the E.C. number, the source of a particular enzyme is usually given, listing the species and the organ or tissue from which it was isolated. 2.4. ENZYMES IN BIOANALYTICAL CHEMISTRY Enzymes can be employed to measure substrate concentrations as well as the concentrations of species that affect the catalytic activity of the enzyme toward its substrate, such as activators and inhibitors. The rst known enzymatic assay was reported by Osann in 1845: hydrogen peroxide (H2O2) was quantitated using the enzyme peroxidase. In 1851, Schonbein reported a detection limit of 1 part H2O2 6 in 2 10 [i.e., 500 parts per billion] using this method! Enzymatic methods

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