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Evolution and Optimum Seeking

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118 <strong>Evolution</strong> Strategies for Numerical Optimization<br />

property (see Rechenberg, 1973) of the evolution strategy can only be proved under the<br />

condition of constant step lengths. With the introduction of the success rule, it is lost,<br />

or to be more precise: the probability of nding the global minimum among several<br />

local minima decreases continuously as a local minimum is approached with continuous<br />

reduction in the step lengths. Rapid convergence <strong>and</strong> reliable global convergence behavior<br />

are two contradictory requirements. They cannot be reconciled if one has absolutely no<br />

knowledge of the topology of the objective function. The 1=5 success rule is aimed at high<br />

convergence rates. If several local optima are expected, it is thus advisable to keep the<br />

(0)<br />

variances large <strong>and</strong> constant, or at least to start with large i <strong>and</strong> perhaps to require a<br />

lower success probability than 1/5. This measure naturally costs extra computation time.<br />

Once one is sure of having located a point near the global extremum, the accuracy can be<br />

improved subsequently in a follow-up computation. For more sophisticated investigations<br />

of the global convergence see Born (1978), Rappl (1984), Scheel (1985), Back, Rudolph,<br />

<strong>and</strong> Schwefel (1993), <strong>and</strong> Beyer (1993).<br />

5.2 A Multimembered <strong>Evolution</strong> Strategy<br />

While the simple, two membered evolution strategy is successful in application to many<br />

optimization problems, it is not a satisfactory method of solving certain types of problem.<br />

As we have seen,by following the 1=5 success rule, the step lengths can be permanently<br />

reduced in size without thereby improving the rate of progress. This phenomenon occurs<br />

frequently if constraints become active during the search, <strong>and</strong> greatly reduce the size of<br />

the success scoring region. A possible remedy would be to alter the probability distribution<br />

of the r<strong>and</strong>om steps in such away astokeep the success probability su ciently<br />

large. To do so the st<strong>and</strong>ard deviations i would have to be individually adjustable.<br />

The contour surfaces of equal probability could then be stretched or contracted along<br />

the coordinate axes into ellipsoids. Further possibilities for adjustment would arise if the<br />

r<strong>and</strong>om components were allowed to depend on each other. For an arbitrary quadratic<br />

problem the rate of convergence of the sphere model could even be achieved if the r<strong>and</strong>om<br />

changes of the individual variables were correlated so as to make the regression line of<br />

the r<strong>and</strong>om vector run parallel to the concentric ellipsoids F (x) =const:, which now lie<br />

at some angle in the space. To put this into practice, information about the topology<br />

of the objective function would have to be gathered <strong>and</strong> analyzed during the optimum<br />

search. This would start to turn the evolution strategy into something resembling one<br />

of the familiar deterministic optimization methods, as Marti (1980) <strong>and</strong> recently again<br />

Ostermeier (1992) have done this is contrary to the line pursued here, which is to apply<br />

biological evolution principles to the numerical solution of optimization problems. Following<br />

Rechenberg's hypothesis, construction of an improved strategy should therefore be<br />

attempted by taking into account further evolution principles.<br />

5.2.1 The Basic Algorithm<br />

When the ground rules of the two membered evolution strategy were formulated in the<br />

language of biology, reference was to one parent <strong>and</strong> one o spring the basic population

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