Operant Variability and the Power of Reinforcement.

A. Neuringer
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引用次数: 26

Abstract

"Since Darwin, the central project of evolutionary biology has been to explain the origin of biodiversity--to determine how novel species and their characteristics have evolved" (Thorton, 2006, p. 157). Operant conditioning can be described in similar terms: Since Skinner, the central project has been to explain how operant behaviors originate and change. To explain biodiversity, on the one hand, and behavioral diversity, on the other, we must consider the variations from which each emerges. This paper is about the causes, consequences, and possible applications of variability, but I begin by noting some parallels in the area of genetics. Continual variation in genetic material provides the bases of all evolved forms of life. Lewis Thomas said this in a more evocative way: "The capacity to blunder slightly is the real marvel of DNA. Without this special attribute, we would still be anaerobic bacteria and there would be no music" (quoted in Pennisi, 1998, p. 1131). Genetic variability, due to mutations in DNA, have many causes including errors during normal replication, insults from chemicals or radiation, jumps or transpositions of genetic materials, and other "spontaneous" changes. In sexually reproducing organisms, another source of continual variation occurs during gamete formation. When genetic material in sperm and egg cells divide, there is random and independent assortment within individual chromosomes and random crossings between portions of maternal and paternal chromosomes. Mutations, jumps, assortments, and crossings are said to occur "randomly," that is, without regard to the current "needs" of an organism or changes that result. However, "random" does not mean without influence or boundaries. The processes that permit and maintain genetic variability have themselves evolved under selection pressures. "Chance favors the prepared genome ... Evolutionary strategies evolve, under the pressure of natural selection; this makes the process of evolution more efficient ... (T)he genome ... (has an) ability to create, focus, tune and regulate genetic variation and thus to play a role in its own evolution" (Caporale, 1999, pp. 1 & 15). A combination of variation and selection at work within the genome itself may best be described as bounded stochasticity , with mutations, mixings and variations occurring stochastically and unpredictably, but within a confined milieu that has been selected and conserved over evolutionary time. As will be seen, similar bounded stochasticity is an attribute of operant behavior as well. A word about terminology. "Stochastic" and "random" will be used synonymously in the present paper, both to indicate a sequence of instances from a defined set, with prediction of the next instance not possible at a level greater than the relative frequencies of members of the set. Imagine, for example, a well-mixed tub filled with 200 red balls, 200 blue balls, and 200 green balls. Balls are selected one at a time with replacement and continual mixing. Prediction of the next color will be no better than 1/3 on average, (200/600), the relative frequencies of each color. If there were 100 red, 200 blue, and 300 green balls, then prediction of green would be correct no more than 1/2 the time on average, (300/600), and so on. Similarly, one can imagine a biased pair of die: Although both dice come up sixes more often than expected (say each does so 1/3 of the time), the outcome of each die roll remains stochastic because having just rolled a six neither raises nor lowers the chances of rolling another six in the future. Although selection may occur stochastically, the emergent instances are limited to members of the set and influenced by their relative proportions or "strengths." As will be shown, there are many types of pressures at work to define and influence the set from which operant instances emerge. All behaviors vary, of course, as do all things physical. But variability plays an especially important role for operant behaviors. …
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操作性变异性和强化的力量。
“自达尔文以来,进化生物学的核心项目一直是解释生物多样性的起源——确定新物种及其特征是如何进化的”(桑顿,2006年,第157页)。操作性条件反射可以用类似的术语来描述:自斯金纳以来,核心项目一直是解释操作性行为是如何产生和改变的。一方面,为了解释生物多样性,另一方面,为了解释行为多样性,我们必须考虑它们产生的差异。这篇论文是关于变异的原因、后果和可能的应用,但我首先注意到遗传学领域的一些相似之处。遗传物质的不断变化为所有进化的生命形式提供了基础。刘易斯·托马斯(Lewis Thomas)用一种更令人回味的方式说过:“轻微犯错的能力是DNA的真正奇迹。如果没有这种特殊的属性,我们仍然是厌氧菌,也不会有音乐”(引用自Pennisi, 1998, p. 1131)。由DNA突变引起的遗传变异有许多原因,包括正常复制过程中的错误、化学物质或辐射的损害、遗传物质的跳跃或转位以及其他“自发”变化。在有性繁殖的生物体中,另一个持续变异的来源发生在配子形成过程中。当精子和卵细胞中的遗传物质分裂时,在单个染色体内存在随机和独立的分类,并且在母染色体和父染色体的部分之间存在随机交叉。突变、跳跃、组合和交叉被认为是“随机”发生的,也就是说,不考虑生物体当前的“需要”或由此产生的变化。然而,“随机”并不意味着没有影响或边界。允许和维持遗传变异的过程本身是在选择压力下进化的。“机会倾向于准备好的基因组……进化策略在自然选择的压力下进化;这使得进化过程更有效率……(T)基因组……(有)创造、集中、调整和调节基因变异的能力,从而在其自身的进化中发挥作用”(Caporale, 1999,第1和15页)。变异和选择的结合在基因组内部起作用,最好被描述为有限的随机性,突变、混合和变异随机地、不可预测地发生,但在一个有限的环境中,在进化的过程中被选择和保存。将会看到,类似的有界随机性也是操作行为的一个属性。关于术语的一句话。“随机”和“随机”将在本文中同义使用,两者都表示来自已定义集合的实例序列,在大于集合成员的相对频率的水平上不可能预测下一个实例。想象一下,例如,一个完全混合的浴缸,里面装满了200个红球、200个蓝球和200个绿球。每次选择一个球,更换和连续混合。对下一个颜色的预测平均不优于每种颜色相对频率的1/3(200/600)。如果有100个红球、200个蓝球和300个绿球,那么预测绿色的正确率平均不超过1/2(300/600),以此类推。类似地,我们可以想象一对有偏差的骰子:尽管两个骰子都比预期的多出6(假设每个骰子都有1/3的概率),但每个骰子的结果仍然是随机的,因为刚刚掷出的6既不会增加也不会降低未来再掷出6的机会。尽管选择可能是随机发生的,但突发事件仅限于集合中的成员,并受其相对比例或“优势”的影响。正如将显示的,有许多类型的压力在定义和影响产生操作实例的集合。当然,所有的行为都是不同的,就像所有的物理事物一样。但可变性在操作性行为中起着特别重要的作用。…
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