Signal probability, reinforcement and signal detection.

Five pigeons were trained to detect differences in light intensity. Two stimuli, S1 and S2, differing in intensity, were arranged on the center key of a three-key chamber according to set probabilities. A peck on the center key turned on the two side keys. When S1 was presented on the center key, a peck on the left key was "correct" and when S2 was presented, a peck on the right key was "correct." Correct responses produced reinforcement and incorrect responses produced 3-second blackout. Detection performance was measured under three procedures. The first was a standard signal-detection design in which the probability of S1 was varied and the number of reinforcements obtained for correct responses to S1 was allowed to covary. In the second procedure, the probability of S1 was again varied but the distribution of reinforcements between the two choices was kept equal. In the third procedure, probability of S1 was held constant while the distribution of reinforcements was varied between the two choices. Changes in response bias were a function of variations in the relative reinforcement ratio for the choice responses and not a function of variations in the probability of stimulus presentation. Discriminability remained constant across the three procedures.     

Effects of the discriminability of alternatives in three-alternative concurrent-schedule performance

Six pigeons were trained on two- and three-alternative concurrent schedules in which the alternatives were signaled by different wavelengths of light on the main pecking key. The schedules were arranged according to a switching-key procedure in which pecks on a white side key produced a 3-s blackout and, intermittently, a change in the variable-interval schedule of food programmed on the main (center) key after the blackout. In Part 1, a two-alternative concurrent variable-interval schedule was arranged in which the alternatives were signaled by 560 nm and 630 nm. Parts 2 and 3 arranged three-alternative concurrent variable-interval schedules with the alternatives signaled by 560 nm, 600 nm, and 630 nm (Part 2) and 560 nm, 623 nm, and 630 nm (Part 3). Within each part, the relative rate of food reinforcers available on the alternatives was varied across a wide range. In all parts of the experiment, the ratios of responses emitted between pairs of alternatives were more extreme than the ratios of reinforcers obtained on the pairs of alternatives, a result termed overmatching. In Parts 2 and 3, generalized matching sensitivities between pairs of alternatives were found to be higher when the reinforcer rate on the third alternative was low than when it was high—an apparent failure of the constant-ratio rule. The data were well described by an extension of the Davison and Jenkins (1985) model, which assumes differing discriminabilities between concurrent-schedule alternatives in combination with a punishing effect of blackout following changeovers.     

Bias in self-evaluation: Signal probability effects

Two experiments examined apparent signal probability effects in simple verbal self-reports. After each trial of a delayed matching-to-sample task, young adults pressed either a “yes” or a “no” button to answer a computer-presented query about whether the most recent choice met a point contingency requiring both speed and accuracy. A successful matching-to-sample choice served as the “signal” in a signal-detection analysis of self-reports. Difficulty of matching to sample, and thus signal probability, was manipulated via the number of nonmatching sample and comparison stimuli. In Experiment 1, subjects exhibited a bias (log b) for reporting matching-to-sample success when success was frequent, and no bias or a bias for reporting failure when success was infrequent. Contingencies involving equal conditional probabilities of point consequences for “I succeeded” and “I failed” reports had no systematic effect on this pattern. Experiment 2 found signal probability effects to be evident regardless of whether referent-response difficulty was manipulated in different conditions or within sessions. These findings indicate that apparent signal probability effects in self-report bias that were observed in previous studies probably were not an artifact of contingencies intended to improve self-report accuracy or of the means of manipulating signal probability. The findings support an analogy between simple self-reports and psychophysical judgments and bolster the conclusion of Critchfield (1993) that signal probability effects can influence simple self-reports much as they do reports about external stimuli in psychophysical experiments.     

PDP再认型实验程序与刺激来源的可鉴别性研究

提出应根据实验程序的不同,把加工分离模型（ＰＤＰ）进一步分为启动型和再认型两类。２个实验考察了刺激来源的可 鉴别性在ＰＤＰ的再认型实验程序中的作用,同时还考察了注意水平、刺激材料和加工水平等因素对词单１刺激项目再认成绩的影 响。结果发现：熟悉感和刺激来源的可鉴别性共同决定了被试在排除测验中的反应;汉字作刺激材料并不影响实验结果。     

“All I remember is the black eye”: A distinctive facial feature harms eyewitness identification

Many crimes occur in which a perpetrator has a distinctive facial feature, such as a tattoo or black eye, but few eyewitness identification (ID) studies have involved such a feature. We conducted an experiment to determine how eyewitness ID performance is impacted by a distinctive facial feature, and how police could deal with this issue. Participants (N = 4,218) studied a target face with or without a black eye, and later viewed a simultaneous photo lineup either containing the target or not. For those who saw a target with a black eye, this feature was either replicated among all lineup members or was removed. The black eye harmed empirical discriminability regardless of replication or removal, which did not differ. However, participants responded more conservatively when the black eye was removed, compared to replication. Lastly, immediate confidence was consistently indicative of accuracy.     

The legacy of Guttman and Kalish (1956): Twenty-five years of research on stimulus generalization

This paper is a selective review of the methods, problems, and findings in the area of operant stimulus generalization over the 25 years since the publication of the original paper by Guttman and Kalish (1956) on discriminability and spectral generalization in the pigeon. The paper falls into five main sections, which encompass the main themes and problems stemming from the Guttman and Kalish work and its immediate successors. The first section addresses the relationship between stimulus generalization and stimulus control, as well as the variety of testing procedures and dependent variables used to measure generalization. The next section reviews the limited literature on the effects of early rearing on the generalization gradient. The relationship between discriminability among test stimuli and the slope of the spectral gradient is discussed in the third section, with emphasis upon recent reassessments of the pigeon's hue discriminability function. The fourth section reviews the topic of inhibitory stimulus control, one which developed with the discovery of the peak shift following intradimensional discrimination training. Problems of definition and measurement are discussed in conjunction with the gradient forms used to index inhibitory control. The last section is devoted to attentional effects and the two principal theories postulated to account for them. A survey of different attentional paradigms is provided and the possible role of constant irrelevant stimuli as a source of control is examined. A brief conclusion summarizes the contribution of the generalization technique toward an understanding of the nature and acquisition of stimulus control.     

An investigation of the differential-outcomes effect within sessions

The differential-outcomes effect is manifest as more accurate performance of a delayed conditional discrimination when alternative choice responses are followed by different reinforcers than when they are followed by the same reinforcer. In Experiment 1, a differential-outcomes effect was demonstrated within sessions by signaling the duration of food access for correct responses with stimuli appearing in conjunction with the sample stimuli. The delayed matching-to-sample performance of 5 pigeons was more accurate when green choice responses (matching a green sample) were followed by 3.5-s food access and red choice responses (matching a red sample) were followed by 0.5-s food access (different-outcome trials) than when the correct choice responses were both followed by 1.5-s reinforcers (same-outcome trials). In Experiment 2, the acquisition of this differential-outcomes effect was characterized by a progressive decrease in rate of forgetting on different-outcome trials and no change in rate of forgetting on same-outcome trials. In addition, accuracy at the shortest delay intervals for both different-outcome and same-outcome trials increased over acquisition, but to a greater extent for different-outcome trials. These data suggest that both memorial and attentional (time-dependent and time-independent) factors contribute to the differential-outcomes effect.