Responses and pauses: discrimination and a choice catastrophe.

Pigeons produced a stimulus change either by responding or by not responding for a specified time period (by pausing). They then had to choose between two responses to obtain food. One choice was correct if the first component had been completed by a response; the other was correct if the component had been completed by a pause. The pigeons usually chose correctly, thereby indicating that they used their own prior behavior as a discriminative stimulus. Fixed pause requirements did not produce equal first component completions by a response and by a pause. To obtain equality, the pause requirement was titrated as a function of current performance. Titration resulted in equal completions and also produced accurate discrimination. In addition to showing that pigeons discriminated whether they had responded or paused, the data displayed and discontinuous functions predicted by catastrophe theory. Another procedure used forced choice rather than titration to produce equal completions by pausing and responding and also showed accurate discrimination of behavior.     

Acquisition of stimulus control while introducing new stimuli in fading.

After establishing discrimination between a red positive stimulus and a green negative stimulus, the lowest intensity colors that restricted all responding to the positive stimulus were determined. Then, two new white lines differing in terms of line orientation were each superimposed on one of the colors and were increased in intensity. Thereafter, the intensity of the colors was decreased and eventually eliminated. Probe stimuli consisting of the lines presented against dark backgrounds were presented before each change of stimulus intensity, and probe responding was used to assess the control acquired by various dimension of the new stimuli during the course of fading. The lines acquired control of responding while they were being introduced, and control was strengthened as the colors were attenuated. Such a locus of acquisition was attributed to the starting intensity of the original controlling stimuli and was explained in terms of stimulus blocking. Finally, using probes while introducing the new stimuli enhanced the acquisition of control by the new stimuli.     

Auditory discrimination: role of time and intensity in the precedence effect.

Rats were trained to respond on a lever adjacent to a sounding speaker (the sound source) when a single click was emitted. A second click (the artificial echo) was presented through a second speaker on the opposite side. In Condition I, the echo (equal in intensity to the source) was delayed from .015 to 32 milliseconds; greater than 75% correct responses were given for delay times between about .040 milliseconds (lower threshold) and 8 milliseconds (upper threshold). In Condition II, the echo (simultaneous with the source) was reduced in intensity relative to the source over a range from 2.5 decibels to 40 decibels; greater than 75% correct responses occurred for intensity reductions greater than 5 decibels. In Condition III, both the intensity and the delay time of the echo were manipulated in a manner analogous to that which would occur under natural conditions; greater than 95% correct responses were given for delay times from 1 to 32 milliseconds. These data indicate that both time and intensity differences are necessary for localization of primary sources, with delay time contributing more at short echo path distances, and intensity differences at long distances.     

Food delivery as a conditional stimulus: Feature-learning and memory in pigeons

Three experiments investigated the learning and memory of discriminations based on presence versus absence of a pre-trial food delivery. In Experiment 1 half the illuminations of a response key were followed by food regardless of the subject's behavior. In one group an extra food delivery preceded only reinforced trials (feature-positive condition), whereas in a second group it preceded only nonreinforced trials (feature-negative condition). Key pecks and approaches revealed more rapid and superior discrimination learning in the first group. Experiment 2 replicated the results of Experiment 1 but yielded no evidence that greater “unexpectedness” of pretrial food conditions facilitates discriminative performance. In Experiment 3, individual pigeons trained on a conditional discrimination exhibited a within-subject feature-positive superiority. Delay between pretrial and trial stimuli interacted with feature-positive versus feature-negative training in both the between-group (Experiment 2) and within-subject (Experiment 3) procedures: performance was decremented at both short and long delays in the feature-positive condition but was decremented only at longer delays in the feature-negative condition. The feature-positive superiority obtained here is incompatible with explanations based on either the general concept of “perceptual organization” or on the conditional nature of feature-negative discriminations.     

The effects of number of sample stimuli and number of choices in a detection task on measures of discriminability

Six pigeons were trained on a conditional discrimination task involving the discrimination of various intensities of yellow light. The research asked whether stimulus—response discriminability measures between any pair of stimuli would remain constant when a third or fourth sample and reinforced response were added. The numbers of different sample stimuli presented and different responses reinforced were two (Part 1), three (Parts 2 and 4), and four (Part 3). Across conditions within parts, the ratios of reinforcers obtainable for correct responses were varied over at least five levels. In Part 5, the numbers of sample stimuli and reinforced responses were varied among two, three, and four, and the reinforcer ratio between consecutive remaining samples was constant at 2:1. It was found that once a particular response had been reinforced, subjects continued to emit that response when the conditional stimulus for that response was no longer presented. Data analysis using a generalization-based detection model indicated that this model was able to describe the data effectively. Four findings were in accord with the theory. First, estimates of stimulus—response discriminability usually decreased as the arranged physical disparity between the sample stimuli decreased. Second, stimulus—response discriminability measures were independent of response—reinforcer discriminability measures, preserving parameter invariance between these measures. Third, stimulus—response discriminability measures for constant pairs of conditional stimuli did not change systematically as conditional stimulus—response alternatives were added. Fourth, log stimulus—response discriminability values between physically adjacent conditional stimuli summed to values that were not significantly different from estimates of the discriminability values for conditional stimuli that were spaced further apart.     

Psychophysics of remembering

We present a new model of remembering in the context of conditional discrimination. For procedures such as delayed matching to sample, the effect of the sample stimuli at the time of remembering is represented by a pair of Thurstonian (normal) distributions of effective stimulus values. The critical assumption of the model is that, based on prior experience, each effective stimulus value is associated with a ratio of reinforcers obtained for previous correct choices of the comparison stimuli. That ratio determines the choice that is made on the basis of the matching law. The standard deviations of the distributions are assumed to increase with increasing retention-interval duration, and the distance between their means is assumed to be a function of other factors that influence overall difficulty of the discrimination. It is a behavioral model in that choice is determined by its reinforcement history. The model predicts that the biasing effects of the reinforcer differential increase with decreasing discriminability and with increasing retention-interval duration. Data from several conditions using a delayed matching-to-sample procedure with pigeons support the predictions.     

A PRELIMINARY EVALUATION OF EMPIRICALLY DERIVED CONSEQUENCES FOR THE TREATMENT OF PICA

Individualized treatment packages were developed for 3 children with high-rate severe pica using a discrimination training paradigm and a behavioral assessment-based procedure known as empirically derived consequences. Children received empirically derived reinforcers for eating under appropriate stimulus conditions (i.e., eating food only from a plate and placemat that served as a discriminative stimulus) and empirically derived punishers for attempts to engage in pica. This treatment package resulted in marked reductions in pica and an increase in appropriate eating for all 3 children in a “baited” analogue condition. In addition, low rates of pica were maintained for 9 months for all 3 children. These results suggest that treatment effectiveness may be enhanced when behavioral assessment data are used to identify potent consequences.     

The behavioral theory of timing: Reinforcer rate determines pacemaker rate

In the behavioral theory of timing, pulses from a hypothetical Poisson pacemaker produce transitions between states that are correlated with adjunctive behavior. The adjunctive behavior serves as a discriminative stimulus for temporal discriminations. The present experiments tested the assumption that the average interpulse time of the pacemaker is proportional to interreinforcer interval. Responses on a left key were reinforced at variable intervals for the first 25 s since the beginning of a 50-s trial, and right-key responses were reinforced at variable intervals during the second 25 s. Psychometric functions relating proportion of right-key responses to time since trial onset, in 5-s intervals across the 50-s trial, were sigmoidal in form. Average interpulse times derived by fitting quantitative predictions from the behavioral theory of timing to obtained psychometric functions decreased when the interreinforcer interval was decreased and increased when the interreinforcer interval was increased, as predicted by the theory. In a second experiment, average interpulse times estimated from trials without reinforcement followed global changes in interreinforcer interval, as predicted by the theory. Changes in temporal discrimination as a function of interreinforcer interval were therefore not influenced by the discrimination of reinforcer occurrence. The present data support the assumption of the behavioral theory of timing that interpulse time is determined by interreinforcer interval.     

Context specificity of conditioned-reinforcement effects on discrimination acquisition

Pigeons were trained on a series of reversals of a simultaneous form discrimination in which the trial outcomes were separated from the choice responses by an 8-s delay interval. Different conditions were defined by the stimuli occurring during the two halves of the delay interval. Discrimination learning was greatly facilitated by having differential stimuli during the delay following correct versus incorrect choices. When the differential stimuli appeared only at the midpoint of the delay, some facilitation occurred relative to when no different stimuli occurred, but there was substantially less facilitation than when the differential stimuli occurred immediately contingent on choice. A reversed-stimulus condition, in which the stimulus at the onset of the delay following a correct choice was the same as that during the last segment of the delay following an incorrect choice, and the stimulus at the onset of the delay following an incorrect choice was the same as that preceding food during the last segment of the delay following a correct choice, also facilitated discrimination learning relative to the nondifferential stimulus conditions.     

Motion as a natural category for pigeons: Generalization and a feature-positive effect

Three groups of pigeons were trained with a modified discriminative autoshaping procedure to discriminate video images of other pigeons on the basis of movement. Birds of all groups were shown the same video images of other pigeons, which were either moving or still. The group to whom food was presented only after moving images learned the discrimination very quickly. A second group, to whom food was given only after still images, and a pseudocategory group, to whom food was presented after arbitrarily chosen stimuli, showed no evidence of discrimination during acquisition training. Extinction conditions led to clear differences in peck rates to moving and still images in the second group but not in the pseudocategory group. The result is related to the feature-positive effect. Generalization tests showed that the discrimination performance was based on visual features of the stimuli but was invariant against changes of size, perspective, brightness, and color. Furthermore, discrimination was maintained when novel images of pigeons under different viewing angles and seven other types of motion categories were presented. It is argued that the discrimination is based not on a common motion feature but on motion concepts or high-order generalization across motion categories.