A NOTE ON TRANSFER OF STIMULUS CONTROL IN THE DELAYED-CUE PROCEDURE: FACILITATION BY AN OVERT DIFFERENTIAL RESPONSE

This case study describes initially unsuccessful attempts to use the delayed-cue procedure to teach conditional discriminations to an individual with moderate mental retardation. The task was matching printed-word comparison stimuli to dictated-name sample stimuli. In three experiments, the subject typically waited for the delayed cue unless differential responses to the dictated samples (repeating the sample names) were required. Hence, the study provides an example of a way to make the delayed-cue method more effective. The stimulus control bases for the results are discussed.     

Assessing control by elements of complex stimuli in delayed matching to sample.

A series of six experiments examined delayed identity matching-to-sample performances of subjects with mental retardation. The stimuli were either one or two simultaneously displayed forms. When the reinforcement contingencies required that only one form exert discriminative control, all subjects achieved high accuracy scores. However, accuracy scores were substantially lower when the contingencies required discriminative control by two forms, suggesting restricted stimulus control. The decline in matching accuracy appeared to reflect selective losses of conditional control by sample stimuli and shifts in control to features of the comparison stimulus displays. The experiments suggest improved techniques for assessing control by complex stimuli and for evaluating the effects of procedures that seek to broaden restricted stimulus control. The results challenge interpretations based on stimulus-generalization decrement or shared attention.     

Delayed constructed-response identity matching improves the spelling performance of students with mental retardation

We assessed the effects of a computerized matching-to-sample procedure on the spelling performances of three students with mental retardation. Initially, the students could 1) match pictures and printed words to one another, and 2) match pictures and printed words to spoken words. However, they could not construct words to either pictures or spoken words (e.g., touch, in order, the letters s->h->o->e given the spoken-word sample Shoe). Word constructions then improved markedly after exposure to delayed constructed-response identity matching (e.g., touch the letters s->h->o->e given the printed-word sample shoe). One subject's oral and written spelling also improved. The results extend previous research by showing multiple positive effects of a computerized spelling intervention. These effects may have occurred in part because of the formation of stimulus classes among pictures, printed words, and spoken words.     

Sample-specific ratio effects in matching to sample

In a symbolic matching-to-sample task, pigeons were trained using sample-specific, fixed-ratio “observing responses.” Subsequently, in a mixed condition, each sample was presented equally often with each ratio requirement, i.e., the ratios were no longer correlated with the samples. In a second experiment, pigeons were trained initially in the mixed condition and subsequently shifted to the sample-specific condition in which the required ratios were correlated with the samples. Results of both experiments suggested joint control of choices by ratio value and by the exteroceptive stimuli. The discriminative properties of the ratios appeared to outweigh absolute ratio-size effects.     

Formation of transitivity in conditional matching to sample by pigeons

Four homing pigeons were trained over 5 months in a zero-delay, “arbitrary” matching-to-sample procedure with sample and comparison stimuli presented on any of three response keys. Birds were also required to complete a fixed-ratio 10 requirement on both sample and comparison stimuli to terminate their presentation. The procedure resulted in the establishment of relations that were not specifically trained and that can be characterized by the property of transitivity in a stimulus equivalence context. This result was in contrast with the findings obtained from most previous research with nonhuman subjects.     

Characteristics of forgetting functions in delayed matching to sample

Performance of pigeons in delayed matching-to-sample procedures was measured in terms of an index of discriminability derived from the difference between logarithms of ratios of choice responses to comparison stimuli following the different sample stimuli. Forgetting functions that plotted discriminability as a function of delay-interval duration were well described by a simple negative exponential function with two parameters, one describing initial discriminability of sample stimuli at zero delay (log d₀) and the other describing rate of decrement in discriminability with increasing delay-interval duration (b). With the difference between wavelength values of the comparison stimuli held constant, a large difference between wavelengths of the sample stimuli resulted in a higher log d₀ value than that for a small difference between sample stimuli, without changing the rate of decrement in discriminability, b. An increase in the fixed-ratio requirement for sample-key responding produced an increase in log d₀ without affecting b, and interpolation of ambient illumination in the delay interval increased b without influencing log d₀. Both parameters changed when intertrial-interval duration was varied. The result of variation in the point of interpolation of ambient illumination in the delay interval indicated that levels of discriminability at longer delays were independent of discriminability levels at earlier delays, consistent with the properties of the exponential function. Functions relating performance to delay-interval duration were suggested to have two characteristics: discriminability of the sample stimuli in the absence of a delay between the stimuli and the behavior they occasion, and rate of attenuation in discriminability with increasing delay-interval duration.     

Extending sequence-class membership with matching to sample

Three normal adults were first trained to point sequentially to each member of several pairs of visual stimuli. This baseline training established one class of stimuli to which subjects responded first, and another class of stimuli to which they responded second. Then, in a matching-to-sample procedure, baseline-sequence stimuli served as samples and new visual stimuli served as comparisons. Subjects were trained to choose one group of new comparisons when the sample was a "first" stimulus from the sequence baseline, and to choose the other new comparison stimuli when the sample was a "second" from the sequence baseline. When the new stimuli were then presented as pairs in the posttest, two subjects pointed to them in sequences predictable on the basis of the stimulus-class membership established during matching to sample. The failure of one subject to demonstrate sequential transfer was shown to be a consequence of the failure of the matching-to-sample procedure to establish stimulus classes. The production of sequences that were not directly trained suggested an empirical approach to the analysis of simple grammatical behavior.     

The effect of logarithmic transformation on estimating the parameters of the generalized matching law

This study examined stimulus class membership established via stimulus-reinforcer relations. Mentally retarded subjects learned conditional discriminations with four two-member sets of visual stimuli (A, B, C, and D). On arbitrary-matching trials, they selected comparison stimuli B1 and B2 conditionally upon samples A1 and A2, respectively, and C1 and C2 conditionally upon B1 and B2, respectively. On identity-matching trials, they selected all stimuli as comparisons conditionally upon identical stimuli as samples. Throughout training, correct selections of A1, B1, C1, and D1 were followed by one reinforcer, R1, and those of A2, B2, C2, and D2 were followed by another, R2. Subsequent tests documented the formation of two four-member stimulus classes, A1-B1-C1-D1 and A2-B2-C2-D2. The class membership of the A, B, and C stimuli could have been based on equivalence relations that resulted from the arbitrary-matching training. D1 and D2 had never appeared on arbitrary-matching trials, however. Their class membership must have been based on relations with R1 and R2, respectively. Results thus confirm a previous finding that stimulus classes can be expanded via stimulus-reinforcer relations. They also define more precisely the potential nature of those classes and the conditions under which class membership can be established.     

Quantification of the effects of chlorpromazine on performance under delayed matching to sample in pigeons.

The effects of four doses of chlorpromazine (dose range 0.5 to 12.5 mg/kg) on performance under a delayed matching-to-sample procedure in pigeons was investigated, using the exponential model of memory (White, 1985). Performance was measured using a bias-free measure of discriminability, log d (Davison & Tustin, 1978), and negative exponential functions were fitted to individual-subject and group data at each dose level. A decrease in matching accuracy was found to be caused by an increase in the rate of forgetting, b, and a decrease in the initial discriminability, log d0. Changes in rate of forgetting and discriminability occurred at doses that had no statistically significant effect on response latency. The exponential model of memory accounted well for the data and provided a useful way of quantifying the effects of chlorpromazine on the processes involved in delayed matching-to-sample performance.     

Base rates versus sample accuracy: competition for control in human matching to sample

People often place undue weight on specific sources of information (case cues) and insufficient weight on more global sources (base rates) even when the latter are highly predictive, a phenomenon termed base-rate neglect. This phenomenon was first demonstrated with paper-and-pencil tasks, and also occurs in a matching-to-sample procedure in which subjects directly experience case sample (cue) accuracy and base rates, and in which discrete, nonverbal choices are made. In two nonverbal experiments, subjects were exposed to hundreds of trials in which they chose between two response options that were both probabilistically reinforced. In Experiment 1, following one of two possible samples (the unpredictive sample), either response was reinforced with a .5 probability. The other sample (predictive) provided reinforcement for matching on 80% of the trials in one condition but in only 20% of the trials in another condition. Subjects' choices following the unpredictive sample were determined primarily by the contingencies in effect for the predictive sample: If matching was reinforced following the predictive sample, subjects tended to match the unpredictive sample as well; if countermatching the predictive sample was generally reinforced, subjects tended to countermatch the unpredictive sample. These results demonstrate only weak control by base rates. In Experiment 2, base rates and sample accuracy were simultaneously varied in opposite directions to keep one set of conditional probabilities constant. Subjects' choices were determined primarily by the overall accuracy of the sample, again demonstrating only weak control by base rates. The same pattern of choice occurred whether this pattern increased or decreased rate of reinforcement. Together, the results of the two experiments provide a clear empirical demonstration of base-rate neglect.     

Effect of delay-interval stimuli on delayed symbolic matching to sample in the pigeon

In Experiment 1, food-deprived pigeons received delayed symbolic matching to sample training in a darkened Skinner box. Trials began with the illumination of the grain feeder lamp (no food sample), or illumination of this lamp, accompanied by the raising of the feeder tray (food sample). After a delay of a few seconds, the two side response keys were illuminated, one with red and one with green light, with positions counterbalanced over trials. Pecking the red (green) comparison produced grain reinforcement if the trial had started with food (no food); pecking red after a no-food sample or green after a food sample was not reinforced. Once matching performance was stable, four stimuli were presented during the delay interval, and their effects on matching accuracy were evaluated. Both illumination of the houselight and the center key with white geometric forms decreased matching accuracy, whereas presentation of a tone and vibration of the test chamber did not. In Experiment 2, pecking the red center key was reinforced with food according to a variable interval schedule. The effects of occasional brief presentations of the four stimuli used in the first experiment on ongoing pecking were assessed. The houselight and form disturbed key pecking, but the tone and vibration did not. Thus, stimuli that interfered with delayed matching also interfered with simple operant behavior. Implications of these results for theories of remembering are discussed.     

Verbal self-reports of delayed matching to sample by humans

Undergraduates participated in two experiments to develop methods for the experimental analysis of self-reports about behavior. The target behavior was the choice response in a delayed-matching-to-sample task in which monetary reinforcement was contingent upon both speed and accuracy of the choice. In Experiment 1, the temporal portion of the contingency was manipulated within each session, and the presence and absence of feedback about reinforcement was manipulated across sessions. As the time limits became stricter, target response speeds increased, but accuracy and reinforcement rates decreased. When feedback was withheld, further reductions in speed and reinforcement occurred, but only at the strictest time limit. Thus, the procedures were successful in producing systematic variation in the speed, accuracy, and reinforcement of the target behavior. Experiment 2 was designed to assess the influence of these characteristics on self-reports. In self-report conditions, each target response was followed by a computer-generated query: “Did you earn points?” The subject reported by pressing “Yes” or “No” buttons, with the sole consequence of advancing the session. In some cases, feedback about reinforcement of the target response followed the reports; in other cases it was withheld. Self-reports were less accurate when the target responses occurred under greater time pressure. When feedback was withheld, the speed of the target response influenced reports, in that the probability of a “Yes” report increased directly with the speed of accurate target responses. In addition, imposing the self-report procedure disrupted target performance by reducing response speeds at the strictest time limit. These results allow investigation of issues in both behavioral and cognitive psychology. More important, the overall order in the data suggests promise for the experimental analysis of self-reports by human subjects.     

Coding responses and the generalization of matching to sample in children.

Two experiments studied the conditions of stimulus control necessary for the generalization of relational matching to sample. Matching required the selection of comparison shapes rotated 90 degrees clockwise from the orientation of the corresponding sample. In Experiment 1, five children were taught to: (a) code the orientations of samples, (b) transform sample codings to account for the 90 degree rotation, and (c) repeat the transformed sample coding response to a comparison. High levels of generalization occurred with a set of novel stimuli for which stable sample-coding responses were initially available. In another novel set, where stable sample-coding responses were not initially available, low levels of generalized matching were recorded. Matching performance improved after stable coding responses were trained. In Experiment 2, two children and three adults were trained in a form of the matching task that produced poor generalization despite the presence of stable sample-coding responses. Retraining to modify the stimulus control exerted by these coding responses produced an immediate improvement in generalized matching to sample. Results suggest that the generalization of matching is dependent on structure of stimulus control that the component responses exert on each other.     

Instructional control of generalized relational matching to sample in children.

Three experiments examined the performance of 4-year-old children in matching geometric stimuli. Performance was developed as a simulation in which all components of the behavior were overt and directly measured. A correct match depended on the state of an instructional stimulus: the background color of the display. In the first two experiments, on nonidentity trials (signified by a green background) the next longer length, larger size, or greater distance was correct. With a blue background, a comparison identical to the sample was correct. In Experiment 3, red was added for which shorter, smaller, or nearer was correct. Also here, on nonidentity trials, if a comparison of the correct length was not presented, the children adjusted their search target to the comparison of the next succeeding size (larger or smaller) so as to maintain a constant matching relation. Subsequently, when exposure to the instructional stimulus was reduced to presentation only at the beginning of each trial, performance simulated matching based on instructions about abstract relations. In all experiments, accurate matching generalized across novel stimuli and reduced exposure to the instructional stimuli.     

Effectiveness and persistence of precurrent mediating behavior in delayed matching to sample and oddity matching with children.

Two kinds of mediating behavior were compared with respect to their effectiveness in variable-delay matching-to-sample and oddity-matching tasks. Each of four 5-year-old children was trained to emit either differential or common mediating responses. The differential mediating response consisted of pressing a specific computer key corresponding to either of two possible sample stimuli (a red or a green square). The common mediating response consisted of pressing one of the two response keys regardless of the sample. The differential-response subjects did not show the typical, delay-related decrease in matching-to-sample performance that characterized the behavior of common-response subjects. An oddity-matching task was then introduced, and subjects were instructed to use the mediating keys however they preferred, including not at all. Differential-response subjects continued to respond on the originally trained mediating keys in response to sample presentation and later reversed their choice responding, thus accommodating the oddity-matching requirements. Common-response subjects continued to emit the previously trained mediating response and experienced limited success in oddity matching. Results were interpreted in terms of stimulus control, instructional control, and experimental history.     

Verbal self-reports about matching to sample: effects of the number of elements in a compound sample stimulus.

Adults' self-reports about their choices in a delayed matching-to-sample task were studied as a function of the number of elements (one, two, or three) in a compound sample stimulus. Signal-detection analyses were used to examine control of self-reports by the number of sample elements, by the speed and accuracy of choices reported about, and by several events contingent on self-reports. On each matching-to-sample trial, a sample element appeared as one of two comparison stimuli. Choice of the matching element, if made within 500 ms of the onset of the comparison stimuli, produced points worth money or chances in a drawing for money, depending on the subject. After each choice, subjects pressed either a "yes" or "no" button to answer a computer-generated query about whether the choice met the point contingency. The number of sample elements in the matching-to-sample task varied across trials, and events contingent on self-reports varied across experimental conditions. In Experiment 1, the conditions were defined by different combinations of feedback messages and point consequences contingent on self-reports, but self-reports were systematically influenced only by the sample-stimulus manipulation. Self-report errors increased with the number of sample elements. False alarms (inaccurate reports of success) were far more common than misses (inaccurate reports of failure), and false alarms were especially likely after choices that were correct but too slow to meet the point contingency. Sensitivity (A') of self-reports decreases as the number of sample elements increased. In addition, self-reports were more sensitive to choice accuracy than to choice speed. All subjects showed a pronounced bias (B'H) for reporting successful responses, although the bias was reduced as the number of sample elements increased and successful choices became less frequent. Experiment 2 demonstrated that the failure of point contingencies to influence self-reports in the first experiment was not due to a general ineffectiveness of the point consequences. Rates of inaccurate self-reports decreased when they resulted in point losses and increased when they resulted in point gains.     

A search for symmetry in the conditional discriminations of rhesus monkeys, baboons, and children.

Procedures for generating arbitrary matching-to-sample performances may generate only conditional discriminations. Rational grounds for this distinction are proposed, based on the properties that any equivalence relation must possess. Empirical tests are described for determining whether subjects trained on conditional discriminations are also engaged in true matching to sample. A series of studies than leads to the conclusion that proof of true matching to sample by monkeys, pigeons, or baboons is yet to be provided. Whether the absence of such proof reflects experiential factors or species-defined limitations is not presently clear.