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.     

Reinforcer efficacy in a delayed matching-to-sample task.

Five domestic hens were exposed to a delayed matching-to-sample task. Conditions 1, 5, and 8 were variable-delay conditions in which five delays (0.25, 1, 2, 4, and 8 s) from the red or green sample to the presentation of the red and green comparison stimuli were presented a number of times during each session. In the fixed-delay condition (Condition 3), each delay was presented for 15 sessions under a Latin square design across birds. When improvements in accuracy across the variable-delay conditions are taken into account, the data were similar under both the variable and fixed delays. In Conditions 2, 4, 6, and 7 sample-reinforcer intervals were held at 8, 8, 4, and 2 s, respectively, while sample-choice intervals were varied within these during each session. With increasing sample-reinforcer interval, both initial discriminability (i.e., with sample-choice delay = 0) and rate of decrement in discriminability decreased. Although the former would be predicted if accuracy depends of the average sample-reinforcer interval, the latter would not. These data show that increasing the sample-choice interval had less effect on matching accuracy than increasing the sample-reinforcer interval did.     

The transfer of contextual control over equivalence classes through equivalence classes: a possible model of social stereotyping.

In Experiment 1, subjects acquired conditional equivalence classes controlled by three male and three female names as contextual stimuli. When equivalence relations were tested using new names not used in training (three male and three female), contextual control remained intact. Thus, generalized control of the composition of conditional equivalence classes by characteristically gender-identified names was shown. A basic analysis of this finding was tested in Experiment 2. Contextual equivalence classes were established using as contextual stimuli nonrepresentational visual figures that were members of additional pretrained three-member equivalence classes. When other stimuli in the pretrained equivalence classes were used as contextual stimuli, the conditional equivalence classes remained intact. Control subjects showed that this effect depended on the equivalence relations established in pretraining. The results show that contextual control over equivalence classes can transfer through equivalence classes. The implications of this phenomenon for social stereotyping are discussed.     

Stability of functional equivalence and stimulus equivalence: effects of baseline reversals

Functional equivalence and stimulus equivalence classes were established, reversed, and tested for stability with college students. Functional stimulus classes were established using a task in which students were trained to say nonsense words in the presence of arbitrarily assigned sets of symbols. Computer-controlled speech-recognition technology was used to record and analyze students' vocal responses for accuracy. After the establishment of stimulus classes was demonstrated with a transfer-of-function test, the effects of reversing selected baseline simple discriminations were assessed during an additional transfer-of-function test and a follow-up test that occurred several weeks later. With the same students, stimulus equivalence classes were established and demonstrated with computerized matching-to-sample procedures. The effects of reversing selected baseline conditional discriminations also were assessed during a postreversal equivalence test and a follow-up test. Both functional stimulus classes and stimulus equivalence were sensitive to contingency reversals, but the reversals with stimulus equivalence closses affected stimulus class organization whereas reversals with functional stimulus classes did not. Follow-up performances were largely consistent with the original baseline contingencies. The similarities and differences between stimulus equivalence and functional equivalence are related to the specific contingencies that select responding in the presence of the stimuli that form the classes.     

An evaluation of a visual–visual successive matching‐to‐sample procedure to establish equivalence classes in adults

Traditionally, behavior analysts have studied stimulus equivalence using a matching‐to‐sample (MTS) preparation. Although researchers have shown the utility of MTS to yield equivalence classes, the procedure requires several prerequisite skills for a learner to accurately respond. Previous research with humans and nonhumans has shown that relational responding can be produced via compound stimulus discrimination and successive matching‐to‐sample (S‐MTS). We conducted four experiments with college students to further evaluate the effectiveness of S‐MTS in the establishment of stimulus relations. S‐MTS trials consisted of the presentation of a single sample stimulus followed by one comparison in a fixed location on a computer screen. Depending upon the sample–comparison relation, participants touched (i.e., go) or did not touch (i.e., no‐go) the comparison stimulus. Following training of the baseline relations (AB/BC), we assessed the emergence of symmetry, transitivity, and equivalence performances (i.e., BA/CB and AC/CA). Results support the utility of the S‐MTS procedure as a possible alternative to traditional MTS. This study has direct implications for participants for whom traditional three‐array MTS procedures may be challenging.     

Transient effects of acquisition history on generalization in a matching-to-sample task

This study examined the role of learning history on the acquisition of a matching-to-sample task. Twelve preschool children learned four stimulus classes through instructions, shaping, or imitation. After reaching criterion, the subjects were exposed to changed discrimination contingencies to determine how each learning history affected the acquisition of responses appropriate to the new contingencies. All subjects reached criterion on the new relations, although the subjects with a shaping history adapted slightly more quickly than those subjects with a history of instructions or imitation. Given sufficient exposure to changed contingencies, rule-driven insensitivity to contingencies was overcome by experience with consequences. This result may be specific to younger subjects, but it suggests that instructions can be used in education without creating insensitivity to contingencies.     

Signal-detection analyses of conditional discrimination and delayed matching-to-sample performance

Quantitative analyses of stimulus control and reinforcer control in conditional discriminations and delayed matching-to-sample procedures often encounter a problem; it is not clear how to analyze data when subjects have not made errors. The present article examines two common methods for overcoming this problem. Monte Carlo simulations of performance demonstrated that both methods introduced systematic deviations into the results, and that there were genuine risks of drawing misleading conclusions concerning behavioral models of signal detection and animal short-term memory.     

Functional classes and equivalence relations

Three adult subjects were taught a set of two-choice simultaneous discriminations, with three positive and three negative stimuli; all possible combinations of positive and negative stimuli yielded nine different pairs. The discriminations were repeatedly reversed and rereversed, the former positive stimuli becoming negative and the former negative stimuli becoming positive. With all subjects, a reversal of the contingencies for one pair of stimuli became sufficient to change their responses to all of the other pairs. The reversals had produced functional stimulus classes. Then, all subjects showed conditional discriminations emerging between members of a functional class; given a sample from one class and comparisons from both classes, they selected the comparison that was in the same class as the sample. Next, 2 of the subjects showed that the within-class conditional relations possessed the symmetric and transitive properties of equivalence relations; after having been taught to relate new stimuli to existing class members, the subjects then matched other class members to the new stimuli. Subsequent tests of two-choice discriminations showed that the conditional discriminations had transferred functional class membership to the new stimuli. The 3rd subject, who did not show equivalence relations among functional class members, was also found to have lost the within-class conditional relations after the equivalence tests.     

Intertrial sources of stimulus control and delayed matching-to-sample performance in humans

Two experiments compared delayed matching-to-sample (DMTS) accuracy under 2 procedures in adults with mental retardation. In the trial-unique procedure, every trial in a session contained different stimuli. Thus, comparison stimuli that were correct on one trial were never incorrect on other trials in that session (or vice versa). In the 2-sample DMTS procedure, the same 2 comparison stimuli were presented on each trial, and their function changed quasi-randomly across trials conditional upon the sample stimulus. Across 2 experiments, 7 of 8 subjects showed the highest overall accuracy under the trial-unique procedure, and no subject showed consistently higher accuracy under the 2-sample procedure. Negative, exponential decay functions fit to logit p values showed that this difference was due largely to the steeper delay-mediated decline in sample control for the 2-sample procedure. Stimulus-control analyses indicated that, under the 2-sample procedure, the selection of the comparison stimulus on Trial N was often controlled by the comparison stimulus selection on Trial N-1 rather than the Trial-N sample stimulus. This source of competing stimulus control is not present in trial-unique procedures. Experiment 2 manipulated intertrial interval duration. There was a small but consistent increase in accuracy as a function of intertrial interval duration under the 2-sample procedure, but not under the trial-unique procedure.     

Instructional effects on performance in a matching-to-sample study

Conducting studies using an undergraduate participant pool is fraught with difficulties. Among them are problems with adequately motivating subjects both to come to the study, and once there, to actively engage the experimental task. Thirty-one college students participated in a matching-to-sample (MTS) study involving substantial training, testing, retraining, and retesting of conditional discriminations and equivalence relations among four 4-member classes of nonsensical words. The study was conducted during the end of the semester, when performance often had been observed to be poorer than at other points in the semester. Eleven of the participants, in addition to standard instructions about the task, received additional instructions specifying molar consequences for high rates of "correct" responses throughout the procedure. This subset of participants displayed markedly improved performance as compared to those who did not receive the additional instructions. Results suggest that specification of molar contingencies improves participants' sensitivity to molecular contingencies within the study. Instructions that specify and increase the consequential functions of feedback provided during MTS trials may be one means of reducing unwanted variability in human MTS performance.     

Symmetry and stimulus class formation in humans: Control by temporal location in a successive matching task

Symmetry refers to the observation that subjects will derive B‐A (e.g., in the presence of B, select A) after being trained on A‐B (e.g., in the presence of A, select B). Whereas symmetry is readily shown in humans, it has been difficult to demonstrate in nonhuman animals. This difficulty, at least in pigeons, may result from responding to specific stimulus properties that change when sample and comparison stimuli switch roles between training and testing. In three experiments with humans, we investigated to what extent human responding is influenced by the temporal location of stimuli using a successive matching‐to‐sample procedure. Our results indicate that temporal location does not spontaneously control responding in humans, although it does in pigeons. Therefore, the number of functional stimuli that humans respond to in this procedure may be half of the number of functional stimuli that the pigeons respond to. In a fourth experiment, we tested this assumption by doubling the number of functional stimuli controlling responding in human participants in an attempt to make the test more comparable to symmetry tests with pigeons. Here, we found that humans responded according to indirect class formation in the same manner as pigeons do. In sum, our results indicate that functional symmetry is readily observed in humans, even in cases where the temporal features of the stimuli prevent functional symmetry in pigeons. We argue that this difference in behavior between the two species does not necessarily reflect a difference in capacity to show functional symmetry between both species, but could also reflect a difference in the functional stimuli each species responds to.     

Testing response-stimulus equivalence relations using differential responses as a sample

This study tested the notion that an equivalence relation may include a response when differential responses are paired with stimuli presented during training. Eight normal adults learned three kinds of computer mouse movements as differential response topographies (R1, R2, and R3). Next, in matching-to-sample training, one of the response topographies was used to select a comparison stimulus B (B1, B2, or B3) conditionally upon presentation of sample stimulus A (A1, A2, or A3), and to select stimulus D (D1, D2, or D3) conditionally upon presentation of stimulus C (C1, C2, or C3). After two sample-comparison-response relations (ABR and CDR) were established, 18 sample-comparison relations were tested (BA, DC, RA, RB, RC, RD, AC, CA, AD, DA, BC, CB, BD, DB, AA, BB, CC, and DD). In the RA, RB, RC, and RD tests, the differential responses (R1, R2, and R3) were used as sample stimuli. All subjects made class-consistent comparison selections in the tests. This study provides evidence that responses may become members of an equivalence class.     

Nodal structure and stimulus relatedness in equivalence classes: post-class formation preference tests

Three experiments used postclass formation within-class preference test performances to evaluate the effects of nodal distance on the relatedness of stimuli in equivalence classes. In Experiment 1, two 2-node four-member equivalence classes were established using the simultaneous protocol in which all of the baseline relations were trained together, after which all emergent relations probes were presented together. All training and testing was done using match-to-sample trials that contained two comparisons. After class formation, the effects of nodal distance were evaluated using within-class preference tests that contained samples and both comparisons from the same class. These tests yielded inconsistent performances for most participants. Experiment 2 replicated Experiment 1, but a third null comparison was used on all trials during class formation. Thereafter, virtually all of the within-class probes, for all participants, evoked performances that were consistent with the predicted effects of nodal distance, that is, the selection of comparisons that were nodally closer to the samples. It appears, then, that the establishment of the equivalence classes with a third null comparison induced control by nodal structure of the classes. Experiment 3 demonstrated the generality of these findings with larger classes that contained more nodal separations, that is, three-node five-member classes. Emergent-relations tests conducted immediately after the within-class tests showed the classes to be intact. Thus, the differential relatedness of stimuli in a class or their interchangeability depended on the content of a test trial: within-class probes occasioned responding indicative of differential strength among the stimuli in the class, while cross-class tests occasioned responding indicative of interchangeability of stimuli in the same class.     

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.     

The nature of standard control in children's matching-to-sample

In Experiment I, six preschool-aged children were given matching-to-sample training with two figures in which they were required to choose one of two comparison stimuli that was identical in shape to the standard stimulus. Following this training, they were given intermittent test trials in which a novel stimulus figure was substituted for the previously correct comparison stimulus. Five of the six subjects consistently chose the substituted stimulus during test trials. Experiment II replicated the findings of Experiment I with three other preschool-aged children. Experiment II also provided controls for the possibility that the subjects of Experiment I were selecting the substituted stimulus because of its novelty. The investigators concluded that eight of the nine subjects were exhibiting the type of control described by Berryman, Cumming, Cohen, and Johnson (1965) as S-delta responding.     

Seasonal variation in pigeon body weight and delayed matching-to-sample performance

The weights of 5 pigeons with free access to food, monitored over 3 calendar years in the laboratory, were found to fluctuate with season. All pigeons were at their heaviest in the winter and were lightest in the summer. Five different pigeons performed a standard delayed matching-to-sample task for 44 weeks from January to November. Their weights were held at 85% of their summer free-feeding weights, making their predicted deprivation level higher in the winter relative to predicted winter free-feeding weights. Slopes of forgetting functions fit to weekly response totals for each pigeon were shallower in winter, showing an improvement in accuracy with longer delays. Thus, delayed matching-to-sample performance may have been affected by the practice of maintaining the pigeons at a constant body weight throughout the calendar year.     

Classroom applications of stimulus equivalence technology

We review basic concepts and methods of stimulus equivalence research and suggest applications in teaching rudimentary language arts skills in the classroom. We describe methods of establishing equivalence-based networks of matching-to-sample, writing, and naming performances. The methods may be used as a supplement to classroom instruction to assess whether standard curriculum-based approaches establish such integrated networks. Methods derived from equivalence research may be useful for remediation when traditional teaching approaches fail. Recent research suggests that direct focus on spelling performances may be required if entire networks of language arts skills are to be acquired. In addition, the equivalence relations themselves may require concentrated teaching in some children.     

Reaction times of younger and older men: effects of compound samples and a prechoice signal on delayed matching-to-sample performances.

Five younger (18 to 23 yrs) and five older (65 to 73 yrs) men were exposed to a series of immediate and delayed (0 to 15 seconds) matching-to-sample problems. Presentation of the pairs of delayed comparison stimuli was either signaled or unsignaled, and the sample contained either 1, 2, or 3 elements, one of which appeared as the positive stimulus. During initial sessions, unlimited time was available to respond. Subsequently, correct responses were reinforced only if they occurred within a specified time limit. A general finding was slower responding with increased delay and with increased number of sample elements. These effects were reduced when the comparison stimuli were signaled and when time limits were in effect. Errors increased as a function of the manipulations of sample complexity and time limits, but did not change systematically when the delay between sample and comparison stimuli was varied. Although the younger men generally responded more quickly than the older ones, men of both ages showed increased speeds when limits were placed on response time, and these changes were maintained when the temporal contingencies were removed.     

Transfer of contextual stimulus function via equivalence class development

In a conditional discrimination, 6 college students arranged six Cyrillic letters into groups of three based upon which of two additional Cyrillic letters (contextual stimuli) was present. All subjects demonstrated symmetry and transitivity within each class of equivalent stimuli. In a second conditional discrimination, two more Cyrillic letters were related to each contextual stimulus. Testing of symmetrical and transitive relations between the original contextual stimulus and the two new ones confirmed the development of two three-member classes of contextual stimuli. Subsequent tests demonstrated that the new contextual stimuli controlled the previously trained sample-comparison relations for all subjects.