Punctuated Equilibrium and Neutral Networks in Genetic Algorithms

Eugen Croitoru, Alexandru–Denis Chipărus, H. Luchian
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Abstract

Taking focused inspiration from biological evolution, we present an empirical study which shows that a Simple Genetic Algorithm (SGA) exhibits punctuated equilibria and punctuated gradualism in its evolution. Using the concept of consensus sequences, and comparing genotype change to phenotype change, we show how an SGA explores candidate solutions along a neutral network - Hamming-proximal bitstrings of similar fit-ness. Alongside mapping the normal functioning of an SGA, we monitor the formation of error thresholds “from above” by starting with a high mutation probability and slowly lowering it, during hundreds of thousands of generations. The formation of a stable consensus sequence is marked by a measurable upheaval in the dynamics of the population, leading to an efficient exploration of the search space in a short time. After the global optimum is found, we can still measure the degree of exploration the SGA performs on that neutral network, and observe punctuated equilibria. We use 11 numerical benchmark functions, along with the Royal Road Function, and a similar bit block Trap Function; the phenomena observed are largely similar on all of them, pointing to a generic behaviour of Genetic Algorithms, rather than problem particularities. Using a consensus sequence (a per-locus-mode chromosome) obscures quasispecies dynamics. This is why we use a per-locus-mean chromosome to measure information change between successive generations, and plot the number and maximal size of Quasispecies and Neutral Networks.
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遗传算法中的间断平衡和中立网络
从生物进化的角度出发,本文提出了一种简单遗传算法(SGA)在进化过程中表现出间断平衡和间断渐进的实证研究结果。使用共识序列的概念,并将基因型变化与表型变化进行比较,我们展示了SGA如何沿着中性网络-相似适应度的汉明-近端位串探索候选解决方案。除了绘制SGA的正常功能外,我们还“从上面”监控错误阈值的形成,方法是从高突变概率开始,然后在数十万代中慢慢降低它。稳定共识序列的形成标志着种群动态的可测量剧变,从而在短时间内有效地探索搜索空间。在找到全局最优后,我们仍然可以测量SGA在该中立网络上执行的探索程度,并观察间断平衡点。我们使用了11个数值基准函数,以及Royal Road函数和一个类似的位块陷阱函数;观察到的所有现象在很大程度上都是相似的,这表明遗传算法的一般行为,而不是问题的特殊性。使用一致序列(每座模式染色体)模糊准种动力学。这就是为什么我们使用每位点平均染色体来测量连续代之间的信息变化,并绘制准物种和中性网络的数量和最大大小。
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