Generalization and response mediation of a conditional discrimination

Fifteen pigeons were given conditional discrimination training in which a colored sample stimulus determined which of two line comparison stimuli (vertical and horizontal) was correct. As part of the conditional discrimination procedure, birds were required to make an "observing response" to the sample stimulus presented on a wide key. The location on this key of the required observing response for the two sample stimuli differed by 0, 3, or 6 in. (0, 7.6, or 15.2 cm) for three groups of birds. Accuracy of conditional discrimination performance was directly related to the amount of separation. In subsequent generalization tests with novel sample stimuli, both observing-response location and comparison responding changed within the same region of the wavelength continuum from that appropriate for one of the training samples to that appropriate for the other. A maintained generalization test (continued reinforcement for training stimuli) revealed this relation more strongly. A test in which observing-response location was the only sample stimulus of a conditional discrimination revealed stimulus control by this observing response, supporting a response mediation interpretation of the data.     

Effects of fixed-ratio sample and choice response requirements upon oddity matching

Three pigeons were trained on oddity matching in which either 1, 4, 8, 16, or 32 sample-key observing responses were required to turn off the sample stimuli and turn on the comparison stimuli. Oddity accuracy increased when the observing-response requirement was raised and decreased when the requirement was lowered. Next, while the observing requirement was maintained at one response, the number of responses required to the comparison stimuli was either 1, 4, 8, 16, or 32. Under these conditions, choice was defined as the comparison that first accumulated the required number of responses. In general, increasing the comparison-response requirement decreased accuracy and lowering the comparison requirement increased accuracy. The fixed-ratio observing requirements appeared to facilitate control by stimuli serving an instructional function.     

Reinforcer frequency and restricted stimulus control.

Stimulus control was evaluated in 3 individuals with moderate to severe mental retardation by delayed identity matching-to-sample procedures that presented either one or two discrete forms as sample stimuli on each trial. On pretests, accuracy scores on one-sample trials were uniformly high. On two-sample trials, the correct stimulus (i.e., the one that subsequently appeared in the comparison array) varied unpredictably, and accuracy scores were substantially lower, suggesting that both sample stimuli did not exert stimulus control on every trial. Subjects were then given training sessions with the one-sample task and with a new set of four stimuli. For two of the stimuli, correct matching responses were followed by reinforcers on a variable-ratio schedule that led to a high reinforcer rate. For the other two stimuli, correct responses were followed by reinforcers on a variable-ratio schedule that led to a substantially lower reinforcer rate. Results on two-sample tests that followed showed that (a) on trials in which comparison arrays consisted of one high reinforcer-rate and one low reinforcer-rate stimulus, subjects most often selected the high-rate stimulus; and (b) on trials in which the comparison arrays were either two high reinforcer-rate stimuli or two low reinforcer-rate stimuli and the samples were one high reinforcer- and one low reinforcer-rate stimulus, accuracy was higher on trials with the high-rate comparisons. These results indicate that the frequency of stimulus control by high reinforcer-rate samples was greater than that by low reinforcer-rate samples. Following more training with the one-sample task and reversed reinforcement schedules for all stimuli, the differences in stimulus control frequencies on two-sample tests also reversed. These results demonstrate experimental control by reinforcement contingencies of which of two sample stimuli controlled selections in the two-sample task. The procedures and results may prove to be relevant for understanding restricted stimulus control and stimulus overselectivity.     

Observing responses in pigeons

Pigeons were trained on an observing-response procedure in which periods of VR 100 and EXT alternated unpredictably during a white light (mixed stimulus). During VR 100, responses on a food-producing key (the first key) were intermittently reinforced. Responses on the observing key (the second key) produced a green light (positive stimulus) when VR 100 was in effect, and a red light (negative stimulus) for EXT. The birds did not respond on either key during the negative stimulus, but they responded on the food-producing key when the positive stimulus appeared. When observing responses produced the positive or negative stimulus on FR, observing responses were maintained until the FR reached a maximum; beyond this, only food-producing responses occurred. When observing responses did not produce either stimulus, the observing-response rates fell to zero. With prolonged exposure to an FR 20 schedule of observing, observing-response rates during EXT were higher than during VR 100. Chlorpromazine hydrochloride decreased the total response output but markedly increased observing-response rates except when it was administered before sessions of observing response extinction.     

MATCHING-TO-SAMPLE PERFORMANCE IN RATS: A CASE OF MISTAKEN IDENTITY?

Three rats had previously acquired a simultaneous matching-to-sample performance with steady and blinking lights. In training, the sample stimulus had always appeared on the middle of three horizontally arranged keys with the comparison stimuli on the side keys. In Experiment 1, the sample stimulus appeared on any of the three keys with the comparison stimuli on the remaining two. The matching-to-sample performance broke down with variable sample and comparison locations; the sample stimulus did not control responding to the comparison stimuli when it appeared on a side key, but it retained control when it appeared on the middle key (as in training). In Experiment 2, the rats were trained with the sample always on the left key. When the sample appeared on either of the trained locations (left or middle key), it retained control for both locations. When the sample then appeared on any of the three keys, as in Experiment 1, sample control did not transfer to the untrained location (right key). The experiments demonstrate that training with fixed sample and comparison locations may establish spatial location as an additional controlling aspect of the stimuli displayed on the keys; stimulus location had become part of the definition of the controlling stimuli. The rats' performance seemed best described as specific discriminations involving the visual stimuli and their spatial locations rather than as identity matching.     

The delay-reduction hypothesis of conditioned reinforcement and punishment: Observing behavior

Pigeons responded in an observing-response procedure in which three fixed-interval components alternated. Pecking one response key produced food reinforcement according to a mixed schedule. Pecking the second (observing) key occasionally replaced the mixed-schedule stimulus with the stimulus correlated with the fixed-interval component then in effect. In Experiment 1, observing was best maintained by stimuli correlated with a reduction in mean time to reinforcement. That finding was consistent with the conditioned-reinforcement hypothesis of observing behavior. However, low rates of observing were also maintained by stimuli not representing delay reduction. Experiment 2 assessed the role of sensory reinforcement. It showed that response rate was higher when maintained by stimuli uncorrelated with reinforcement delay than when the stimuli were correlated with a delay increase. This latter result supports a symmetrical version of the conditioned-reinforcement hypothesis that requires suppression by stimuli correlated with an increase in time to reinforcement. The results were inconsistent with hypotheses stressing the reinforcing potency of uncertainty reduction.     

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.     

Memory codes in pigeon short-term memory: Effects of varying the number of sample and comparison stimuli

In a delayed conditional discrimination task, pigeons can remember either some aspect of the conditional stimulus (i.e., they can code retrospectively) or some aspect of the stimulus to which they will respond at the end of the delay (i.e., they can code prospectively). To determine the nature of the memory code, we varied the number of possible sample stimuli (two or four) and the number of possible comparison stimuli (two or four) factorially across groups. Birds in all four groups were initially trained on a zero-delay, conditional discrimination with lines (vertical and horizontal) and/or shapes (circle and triangle), and were then tested with longer delays between sample offset and comparison onset. Acquisition of the conditional discrimination was affected by both the number of sample and comparison stimuli: birds were slower to reach criterion the greater the number in either stimulus set. During delay testing, however, only the number of comparisons affected performance. Overall, retention was poorer with four comparisons than with two. These data provide evidence for prospective coding in pigeon short-term memory.     

Degree of representation of the matching concept in pigeons (Columba livia)

In Experiment 1, 12 pigeons (Columba livia) were trained on a simultaneous matching-to-sample task with 2 stimuli and then tested with 2 novel stimuli. Half of the birds were trained with a fixed ratio schedule requirement of 1 (FR1) or 20 (FR20) pecks on the sample stimulus. None of the birds showed any evidence of concept-mediated transfer. In Experiment 2, 12 pigeons were trained with 3 stimuli and then tested with the same novel stimuli used in Experiment 1. Half of the birds in each group were trained with either an FR1 or FR20 requirement on the sample stimulus. Two of the FR20 birds showed high levels of transfer to the novel stimuli similar to that of monkeys in a previous study.     

A procedure for generating differential "sample" responding without different exteroceptive stimuli

Sidman (1994, 2000) suggested that responses as well as stimuli can join equivalence classes, a hypothesis difficult to test because differential responding typically requires different stimuli. The present experiments describe a procedure with pigeons that avoids this potential confounding effect. In Experiment 1, spacing two responses 3 s apart (a differential-reinforcement-of-low-rate [DRL] schedule) to a white stimulus on some trials produced food or the comparison stimuli in a matching task, whereas pecking 10 or more times with no temporal restrictions (a fixed-ratio [FR] schedule) produced the same effect on other trials. Completing the alternative (unscheduled) requirement terminated the white stimulus and repeated the trial. Following such errors, pigeons learned to switch to the alternative response pattern on the repeat trials. In addition, the correct response pattern functioned as a conditional cue for comparison choice. In Experiment 2, mixed DRL-FR training was preceded by two-sample/two-alternative matching-to-sample with DRL and FR sample-response requirements. In a subsequent transfer test in which the correct response pattern to white served as the sample, pigeons preferentially chose the comparison previously reinforced following that pattern in the baseline task. This "unsignaled response" procedure may be useful for assessing whether differential responses can be members of acquired equivalence classes.     

Performance of pigeons on delayed simple and conditional discriminations under equivalent training procedures

A pair of experiments investigated the short-term memory of pigeons under delayed simple and conditional discriminations. Trial sequences in both discriminations consisted of a color as the sample stimulus, a memory interval, a line orientation as the test stimulus, and a trial outcome, which was either food reinforcement or blackout. Pecking rates during the test stimulus defined discrimination performance. In the simple discrimination, the sample provided the necessary information regarding the subsequent trial outcome. In the conditional discrimination, the sample and test stimuli conjointly provided this information. In Experiment 1, the two procedures were compared with independent groups of pigeons. In Experiment 2, the comparison was made within subjects. The simple discrimination was acquired more quickly and was performed better with a memory requirement. Introduction of long delays disrupted performance even at shorter delays in both discriminations. Postulation of prospective as well as retrospective mediating processes facilitates the interpretation of these results.     

Effects of stimulus presentation order during auditory–visual conditional discrimination training for children with autism spectrum disorder

Children with autism spectrum disorder are typically taught conditional discriminations using a match‐to‐sample arrangement. Consideration should be given to the temporal order in which antecedent stimuli (the sample and comparison stimuli) are presented during match‐to‐sample trials, as various arrangements have been used in the extant literature. The purpose of the current study was to compare the effects of four stimulus presentation orders on the acquisition of auditory–visual conditional discriminations. The study included participants from a clinically relevant population (three children with autism spectrum disorder), employed clinically relevant teaching procedures, and included two presentation formats not included in previous comparison evaluations (simultaneous and sample‐first with re‐presentation conditions). Results were found to be learner‐specific; that is, a different stimulus presentation format was most efficient for each participant. We provide suggestions to evaluate stimulus control topographies and enhance experimental control in match‐to‐sample arrangements.     

Use of an ambiguous-sample procedure to establish a cue to forget in pigeons

Pigeons were trained on a variation of the matching-to-sample task in which on double-sample trials two samples, one associated with each of the comparison stimuli, were presented successively. Responding to the comparison associated with the first sample was reinforced on half the double-sample trials, and responding to the comparison associated with the second sample was reinforced on the remaining half. One of two postsample stimuli was presented following the termination of each colored sample. A vertical line was presented after a correct or target sample, and a horizontal line was presented after an incorrect or interfering sample. With extended training, each bird demonstrated above-chance accuracy on double-sample trials, providing prima facie evidence that one or both of the postsample stimuli exerted control over matching behavior. Experiment 2 provided evidence that the horizontal line functioned as a cue to forget the code activated by the preceding sample stimulus. It was concluded that a condition sufficient to establish a postsample stimulus as a cue to forget is that the postsample immediately follow presentation of a sample that, if it were to control test responding, would lead to nonreinforcement.     

A relational differential outcomes effect: pigeons can classify outcomes as “good” and “better”

In a conditional discrimination each of two sample stimuli indicates which of two comparison stimuli is correct. When correct choice following each conditional stimulus is followed by a different outcome (one kind of food following one, a different kind of food following the other) it often facilitates acquisition and improves memory. In transfer designs, in which two different conditional discriminations are followed by the same two differential outcomes, outcome expectation can be shown to be sufficient for comparison choice. That is, the samples from one conditional discrimination are matched to comparisons from the other conditional discrimination based on the common outcomes alone. In the present study we asked if for pigeons the relative value of the differential outcomes (higher versus lower value) can serve as the basis for comparison choice, independent of other characteristics of the outcomes and of differential sample responding. That is, would different outcomes that could be described as “good” and “better” form two stimulus classes. For one conditional discrimination, the differential outcomes involved differential probability of reinforcement for choice of the correct comparison stimulus (0.80 vs. 0.20 for correct choice of the two comparisons, respectively). For the other conditional discrimination, the differential outcomes involved differential responding to the two comparison stimuli (5 pecks vs. 20 pecks to the correct comparisons, respectively). On test trials, when conditional stimuli from the two conditional discriminations were interchanged and the relative value of the differential outcomes could serve as the only basis for comparison choice, we found positive transfer. The results indicate that relational attributes of outcomes can serve as effective cues for comparison choice.     

Transfer of oddity-from-sample performance in pigeons

Four pigeons were trained on a modified three-key oddity-from-sample task in which an observing response to the sample (center-key) stimulus lighted a single comparison (side-key) stimulus. If the comparison stimulus was different from the sample stimulus, a single peck to the lighted comparison was reinforced. If the comparison and sample stimuli were identical, the pigeons had to refrain from pecking the comparison for 4.6 seconds to terminate the matching comparison and to produce immediately a nonmatching comparison on the remaining side key. Each peck to the matching comparison reset the 4.6-second delay interval. Three hues were used during acquisition. During tests for transfer of the oddity performance, two novel hues were substituted either individually or together for one or two of the original training hues. For three birds, latencies to novel nonmatching hues were identical to baseline nonmatching latencies. Latencies to novel matching hues were shorter than baseline matching latencies but were consistently longer than novel nonmatching latencies. These transfer data demonstrate that the pigeons learned the oddity concept.     

Protocol analysis of the correspondence of verbal behavior and equivalence class formation.

In two equivalence experiments, a "think aloud" procedure modeled after Ericsson and Simon's (1980) protocol analysis was implemented to examine subjects' covert verbal responses during matching to sample. The purpose was to identify variables that might explain individual differences in equivalence class formation. The results from Experiment 1 suggested that subjects who formed equivalence classes described the relations among stimuli, whereas those not showing equivalence described sample and comparison stimuli as unitary compounds. Because Experiment 1 only demonstrated a correlation between describing stimulus compounds and the absence of equivalence classes, a second study was conducted. In Experiment 2, equivalence class formation was brought under experimental control through pretraining manipulations that facilitated responding either to stimulus compounds or to relations among stimuli. The results demonstrated that a history of describing stimulus compounds, when compared with describing the relations among the stimuli, interfered with the emergence of stimulus equivalence. These findings clarify individual differences in stimulus equivalence. They also demonstrate the utility of analyzing verbal reports to identify possible variables that can be manipulated experimentally.     

Emergent conditional discrimination in children: Matching to compound stimuli

This study reports two experiments that first taught preschool children identity-matching to compound sample and compound comparison stimuli. A compound stimulus consisted of a colour and a form superimposed on one another. Test sessions assessed whether children related the form and colour elements of a particular compound stimulus. The test for this was matching to sample in which an arbitrary conditional discrimination was required. A majority of the children selected the correct colour comparison in the presence of each form sample. The children also showed the reverse sample-comparison relations: they matched form comparisons to the corresponding colour samples, respectively. In the context of these arbitrary relations, new colours were paired with the form elements of the samples (Experiment 1), and new form elements were paired with the colour elements of the comparisons (Experiment 2). Subsequent tests assessed whether the new stimulus elements had control over responding when presented as single samples or comparisons. Test results showed that most subjects were able to relate the new stimulus elements to the corresponding colour and form elements, respectively. The study demonstrated that matching to compound stimuli in training and testing conditionsMaygenerate conditional relations between the individual stimulus elements.     

Conditional discrimination in mentally retarded adults: the effect of training the component simple discriminations.

Two subjects with retardation who exhibited generalized identity matching, but who had extensive histories of failure to acquire arbitrary matching, were exposed to a series of conditions designed to train separately the components of a two-choice conditional discrimination. First, the successive discrimination between the sample stimuli was established by programming a different schedule of reinforcement in the presence of each sample stimulus. Schedule performance was acquired and maintained by both subjects, but neither acquired arbitrary matching. To train the simultaneous discrimination between the comparison stimuli, 1 subject was then exposed to a series of simple discrimination reversals and subsequently failed to acquire arbitrary matching. Both subjects acquired arbitrary matching under a procedure that maintained both the sample and the comparison discrimination by first presenting entire sessions composed of one sample-comparison relation and then gradually reducing the number of consecutive trials with the same sample until sample presentation was randomized (schedule performance was maintained). Removal of the schedule requirement had no effect on arbitrary matching accuracy. Both subjects subsequently demonstrated control by relations symmetric to the trained relations.     

Stimulus equivalence and transitive associations: A methodological analysis

When a number of two-stimulus relations are established through training within a set of stimuli, other two-stimulus relations often emerge in the same set without direct training. These, termed "transitive stimulus relations," have been demonstrated with a variety of visual and auditory stimuli. The phenomenon has served as a behavioral model for explaining the emergence of rudimentary comprehension and reading skills, and the development of generative syntactic repertoires. This article considers the range of relations that can arise between a given number of stimuli in a class, the number of directly established two-stimulus relations necessary for the emergence of transitive relations, the forms that training sets of stimuli can take, and the number of transitive two-stimulus relations that can be induced without direct training. The procedures needed to establish and assess transitive stimulus control, the possible interactions between the training and testing procedures, and the constrainst these interactions place upon the analysis of transitive stimulus control are also examined. The present analysis indicates that in a transitivity test, choice among such stimuli may be controlled by (1) the relation between the sample and the positive comparison stimulus (transitive stimulus control), (2) the relation between the sample and the negative comparison stimulus (S- rule control), and (3) possible discriminative properties that may inadvertently be established in the positive and negative comparison stimuli (valence control). Methods are described for distinguishing these three forms of stimulus control.