Control of adolescents' arbitrary matching-to-sample by positive and negative stimulus relations.

In Experiment 1, four developmentally delayed adolescents were taught an A-B matching-to-sample task with nonidentical stimuli: given Sample A1, select Comparison B1; given A2, select B2. During nonreinforced test trials, appropriate matching occurred when B stimuli appeared as samples and A stimuli as comparisons, i.e., the sample and comparison functions were symmetrical (B-A matching). During A-B or B-A matching test trials in which familiar samples and correct comparisons were presented along with novel comparisons, the subjects selected the correct comparisons. In tests with familiar samples and both incorrect and novel comparisons, subjects selected the novel comparisons, demonstrating control by both positive ("matching") and negative ("nonmatching") stimulus relations in A-B and B-A arrays. In Experiment 2, 12 developmentally delayed subjects were taught a two-stage arbitrary-matching task (e.g., A-B, C-B matching). Test sessions showed sample-comparison symmetry (e.g., B-A, B-C matching) and derived sample-comparison relations (e.g., A-C, C-A matching) for 11 subjects. These subjects also demonstrated control by positive and negative stimulus relations in the derived relations.     

Establishing Arbitrary Stimulus Classes via Identity-matching Training and Non-reinforced Matching with Complex Stimuli

The present study investigated whether training on an identity match-to-sample task followed by non-reinforced matching probes with complex stimuli leads to the emergence of multiple arbitrary matching performances and arbitrary stimulus classes in preschool children. In Experiment 1, eight subjects were trained on a colour-matching task (A-A). Then they received tests with complex AB and AC colour-form stimuli (AB-A, B-AB; AC-A, C-AC). These tasks were designed to help subjects respond to both elements of each complex stimulus. Subsequent B-A, C-A, A-B, A-C, B-C, and C-B tests revealed that all subjects had acquired class-consistent colour-form and form-form relations. Experiment 2 examined whether these results could be replicated when subjects were encouraged to respond to the colour elements of some (AB) complex stimuli and to the form elements of other (AC) stimuli. The procedures were the same as in Experiment 1 except that during the first test only A-AB and C-AC tasks were used. Six of eight subjects demonstrated all tested relations.     

Emergent Simple Discriminations and Conditional Relations in Children, Intellectually Impaired Adults,

Previous research has shown that when, under non-reinforced conditions, stimuli are added to S+ and S- stimuli in simultaneous discrimination tasks, transfer between paired stimuli is likely to occur. The present study examined whether this procedure also leads to the formation of conditional relations between paired stimuli. In Experiments 1, 2, and 3, normal pre-school children were trained on a simultaneous discrimination task with A1 reinforced and A2 not reinforced (A1+/A2- ). Then they received two tests (no programmed consequences): one with B stimuli superimposed on the A stimuli (A1B1/ A2B2), and one with B stimuli only (B1/B2). Subjects who selected A1B1 and B1 also received conditional discrimination tests: one with B1 or B2 as samples and A1 and A2 as comparisons (B-A), and one in which the functions of these stimuli were reversed (A-B). Intellectually impaired adults and normal adults served in Experiments 4 and 5, respectively. These experiments were basically the same except that the subjects were also given the opportunity to demonstrate transfer from B to C via BC (B1C1/B2C2 and C1/C2 tests). Most children (75%) and intellectually impaired adults (75%) treated the conditional discrimination probe tasks as simple discriminations and typically selected the trained and derived S+ stimuli. The remaining children, intellectually impaired adults, and all normal adults related all directly and indirectly linked stimuli of the same functions conditionally to one another (A-B, B-C, A-C, and vice versa). The present findings suggest that, as humans develop, conditional stimulus relations may emerge from tasks and stimulus configurations that are increasingly remote from traditional conditional discrimination tasks.     

Naming in conditional discrimination and stimulus equivalence.

Using a matching-to-sample procedure, McIntire, Cleary, and Thompson (1987) taught monkeys the conditional relations A1-R1-A1-R1, A2-R2-A2-R2, A1-R1-B1-R1, A2-R2-B2-R2, B1-R1-C1-R1, and B2-R2-C2-R2, where the first and third terms in each relation refer to the sample and comparison stimuli, respectively, and the second and last terms refer to the emission of a distinctive pattern of responding. The subjects were then tested for the emergent relations A-C, C-A, B-A, C-B, and B-B, with the differential response produced by a given stimulus during training also emitted on test trials (e.g., A1-R1-C1-R1). The performances of both subjects were as accurate on the tested relations as they had been on the trained relations. The new relations were characterized as demonstrations of stimulus equivalence. However, the conditional discrimination literature shows that such training procedures generate control of comparison selection by the differential response patterns. Therefore, no emergent relations were demonstrated because all of the trained response-stimulus relations were preserved on test trials. This paper suggests that these procedures do not provide an appropriate analogy for the kind of emergent stimulus-stimulus relations exhibited by human subjects in equivalence studies and outlines a paradigm for assessing the relative influence of stimulus-stimulus and response-stimulus relations.     

A functional analytic approach to computer-interactive mathematics

Following a pretest, 11 participants who were naive with regard to various algebraic and trigonometric transformations received an introductory lecture regarding the fundamentals of the rectangular coordinate system. Following the lecture, they took part in a computer-interactive matching-to-sample procedure in which they received training on particular formula-to-formula and formula-to-graph relations as these formulas pertain to reflections and vertical and horizontal shifts. In training A-B, standard formulas served as samples and factored formulas served as comparisons. In training B-C, factored formulas served as samples and graphs served as comparisons. Subsequently, the program assessed for mutually entailed B-A and C-B relations as well as combinatorially entailed C-A and A-C relations. After all participants demonstrated mutual entailment and combinatorial entailment, we employed a test of novel relations to assess 40 different and complex variations of the original training formulas and their respective graphs. Six of 10 participants who completed training demonstrated perfect or near-perfect performance in identifying novel formula-to-graph relations. Three of the 4 participants who made more than three incorrect responses during the assessment of novel relations showed some commonality among their error patterns. Derived transfer of stimulus control using mathematical relations is discussed.     

The development of functional and equivalence classes in high-functioning autistic children: the role of naming.

The development of functional and equivalence classes was studied in four high-functioning, preschool-aged autistic children. Initially, all subjects failed to demonstrate match-to-sample relations indicative of stimulus equivalence among two three-member classes of visual stimuli. Then, 2 subjects showed emergence of those relations after they were taught to assign the same name to all members in each class. Next, subjects were taught names for new stimuli outside the match-to-sample format. On subsequent match-to-sample tests, 2 subjects demonstrated untrained conditional relations among the stimuli given a common name. New, unnamed stimuli were then related via match-to-sample training to stimuli from sets of named stimuli. Tests for emergent conditional relations between the new unnamed stimuli and the named stimuli yielded positive results for 1 subject and somewhat mixed results for 3 subjects. Finally, without naming, 2 subjects developed stimulus equivalence among two new three-member classes of visual stimuli. These data suggest that naming may remediate failures to develop untrained conditional relations, some of which are indicative of stimulus equivalence.     

Mediation process and the acquisition of language

Summary Two experiments were conducted with chaining paradigm in which three lists were differentiated in semantic organization. In Experiment I, chaining (A-B, B-C, A-C), pseudo-chaining (A-B, B'-C, A-C) and non-chaining (A-B, D-C, A-C) conditions produced no difference in the performance on the A-C list in Stage III and A-B recall in Stage IV was the same for all conditions, corresponding to the same performance on the A-B list in Stage I. The findings were confirmed by Experiment II in which two types of mediators (preposition versus contentive) were used in chaining paradigm. No evidence of mediated facilitation was found. The results were discussed with regard to whether mediation process could provide an adequate explanatory device of language acquisition process.The study was supported by a grant from Deutsche Forschungsgemeinschaft. I am very grateful to Prof. Dr. W. Metzger for his useful suggestions.     

Primacy effects induced by temporal or physical context shifts are attenuated by a preshift test trial

When subjects are sequentially trained with a cue (A) paired separately with two outcomes (B and C) in different phases (i.e., A-B pairings followed by A-C pairings) testing in the training context after short retention intervals often reveals recency effects (i.e., stronger influence by A-C). In contrast, testing after long retention intervals or testing in a context different from that of training sometimes reveals primacy effects (A-B). Three experiments were conducted using rats in a Pavlovian conditioned bar-press suppression preparation to ascertain whether a nonreinforced test trial in the training context soon after training can attenuate this shift to primacy. Experiment 1 demonstrated that exposure to A shortly after both phases of training, but prior to a long retention interval, can attenuate shifts from recency to primacy otherwise observed with a long retention interval. Experiment 2 showed that exposure to A in the training context can also eliminate the shift from recency to primacy otherwise produced by shifting the physical context between training and test. Experiment 3 discredited a potential account of the results of Experiments 1 and 2. The effects observed in Experiment 1 and 2 are interpreted as early testing in the training context serving to initiate rehearsal of the A-C association due to the temporal proximity of A-C training.     

The development of derived stimulus relations through training in arbitrary-matching sequences

Five-year-old children were taught three-stage sequences of arbitrary matching: A-C, B-C, A-D; A-C, B-D, B-C; or A-C, A-D, B-C. Each stage refers to a sample-comparison relation between stimuli. Unreinforced test probes revealed untrained arbitrary matches (B-D, A-D, and B-D, respectively), derivable by substitution of stimuli with a common sample or comparison function. Additional probes revealed further untrained sample-comparison relations derivable by substitution and identity, including the commuted relations D-B, D-A, and D-B, respectively. These processes may have relevance to conceptual and verbal behavior.     

Acquisition of matching to sample via mediated transfer

Two severely retarded Down's-syndrome boys learned a matching-to-sample performance through mediated transfer. The transfer paradigm involved three sets of stimuli, one auditory set (A) and two visual sets (B and C). The subjects were taught directly to do B-A and C-B matching, but experienced no direct association between C and A. They acquired the ability to do C-A matching without having been taught that performance directly. They also learned indirectly to name some of the visual stimuli, but naming was apparently not the mediator in the emergent C-A matching. The use of words and letters as stimuli highlighted the possible relevance of mediated associations in the indirect acquisition of elementary reading comprehension and oral reading. The acquisition of matching via mediated transfer also raised some new considerations concerning the role of coding responses in arbitrary matching to sample.     

Conditional relations with compound abstract stimuli using a go/no-go procedure

The aim of this study was to evaluate whether emergent conditional relations could be established with a go/no-go procedure using compound abstract stimuli. The procedure was conducted with 6 adult humans. During training, responses emitted in the presence of certain stimulus compounds (A1B1, A2B2, A3B3, B1C1, B2C2, and B3C3) were followed by reinforcing consequences (points); responses emitted in the presence of other compounds (A1B2, A1B3, A2B1, A2B3, A3B1, A3B2, B1C2, B1C3, B2C1, B2C3, B3C1 and B3C2) were not (i.e., extinction). During subsequent tests of emergent relations, new configurations (BA, CB, AC, and CA relations) were presented, formed by the recombination of training stimuli and structurally resembling tests usually employed in stimulus equivalence studies. Results showed that all 6 participants displayed immediate emergence of relations consistent with symmetry. Four participants exhibited emergent relations consistent with both transitivity and equivalence. These results indicate that a go/no-go procedure with compound stimuli can establish emergent conditional relations, thus providing a procedural alternative to the matching-to-sample procedures commonly used in studies of stimulus equivalence.     

Derived false memories using a respondent‐type (ReT) procedure

The present investigation used a respondent‐type (ReT) training procedure to generate derived false memories. A one‐to‐many ReT training procedure was implemented in order to establish two stimulus equivalence classes, each consisting of one shape and 24 random words (i.e., Class 1 and Class 2). A partial test for stimulus equivalence with a subset of stimuli from each class followed. Failing an equivalence test resulted in additional ReT training and equivalence testing on new subsets of stimuli. After passing an equivalence test, participants were presented with 12 study‐list words from Class 1 for memorization, followed by a distraction task. Finally, free recall and recognition tests for the study‐list words were implemented. False recall and false recognition were more frequent for nonstudied Class 1 words than for nonstudied Class 2 words. These derived false‐memory effects were more pronounced among those participants exhibiting more training and testing cycles and higher accuracy on stimulus equivalence tests. Furthermore, false recall and false remembering of nonstudied Class 1 words were more frequent for words that had been equivalence‐tested than for words that had not been equivalence‐tested. These results show how responses to contiguous stimuli could produce derived false memories and also highlight the role played by the equivalence test in increasing their emergence.     

Function transfer in human operant experiments: the role of stimulus pairings

Although function transfer often has been studied in complex operant procedures (such as matching to sample), whether operant reinforcement actually produces function transfer in such settings has not been established. The present experiments, with high school students as subjects, suggest that stimulus pairings can promote function transfer in conditions that closely approximate those of matching to sample. In Experiment 1, the subjects showed transfer of operant responding from three geometric figures (C1, C2, C3) to three colored shapes (B1, B2, B3) when the latter were paired with the former. Experiment 2 involved two groups of subjects. In the matching group, subjects matched the colored shapes with the geometric figures; in the yoked group, the shapes were merely paired with the geometric figures, and the schedule of stimulus pairing was yoked to the performance of the subjects in the matching group. Both groups of subjects showed function transfer. Experiment 3 documented function transfer from C stimuli to B stimuli through indirect stimulus pairings (A-B, A-C). In Experiment 4, function transfer was obtained even though the subjects vocalized continuously during the pairing trials, presumably preventing covert verbalization that might mediate transfer effects. Our results are consistent with a Pavlovian account and raise difficulties for current operant theories of function transfer.     

Review of Cultural Psychology,by Steven J. Heine

Summary

An A-B, B-C, A-C mediation paradigm was used to investigate observational learning of attitudes in a laboratory situation. The A-B stage involved the learning of dissyllables as responses to instances of three concepts. In the B-C stage, Ss observed a model apparently receiving different levels of shock in association with the dissyllables. In the A-C stage, Ss pulled a lever after the presentation of each of the previously learned concept instances and an equal number of new instances of the same concepts. During a second presentation, Ss gave evaluative ratings of the concept instances. The latency, speed, and amplitude of the lever pull response were not affected by the experimental manipulations. With respect to ratings, instances of concepts associated with shock to the model were significantly more disliked than instances of concepts not paired with shock to the model.     

The relationship between differential stimulus relatedness and implicit measure effect sizes

Implicit measures have been hypothesized to allow researchers to ascertain the existence and strength of relations between stimuli, often in the context of research on attitudes. However, little controlled behavioral research has focused on whether stimulus relations, and the degree of relatedness within such relations, are indexed by implicit measures. The current study examined this issue using a behavior‐analytic implicit‐style stimulus relation indexing procedure known as the Function Acquisition Speed Test (FAST). Using a matching‐to‐sample (MTS) procedure to train stimulus equivalence relations between nonsense syllables, the number of iterations of the procedure was varied across groups of participants, hence controlling stimulus relatedness in the resulting equivalence relations. Following final exposure to the MTS procedure, participants completed a FAST. Another group of participants was exposed to a FAST procedure with word pairs of known relatedness. Results showed that increasing relatedness resulted in a linear increase in FAST effect size. These results provide the first direct empirical support for a key process‐level assumption of the implicit literature, and offer a behavior‐analytic paradigm within which to understand these effects. These results also suggest that the FAST may be a viable procedure for the quantification of emergent stimulus relations in stimulus equivalence training.     

A transfer of self-discrimination response functions through equivalence relations

The present study tested the idea that human self-discrimination response functions may transfer through equivalence relations. Four subjects were trained in six symbolic matching-to-sample tasks (if see A1, choose B1; A1-C1, A2-B2, A2-C2, A3-B3, A3-C3) and were then tested for the formation of three equivalence relations (B1-C1, B2-C2, B3-C3). Two of the B stimuli (B1 and B2) were then used to train two different self-discrimination responses using either detailed instructions (Subjects 1 to 3) or minimal instructions (Subject 4) on two complex schedules of reinforcement (i.e., subjects were trained to pick the B1 stimulus if they had not emitted a response, and to pick the B2 stimulus if they had emitted one or more responses on the previous schedule). All 4 subjects showed the predicted transfer of self-discrimination response functions through equivalence relations (i.e., no response on the schedule, pick C1; one or more responses on the schedule, pick C2). Subjects also demonstrated this transfer when they were required to discriminate their schedule performance before exposure to the schedule (i.e., “what I intend to do”). Four control subjects were also used in the study. Two of these (Subjects 5 and 6) were not exposed to any form of matching-to-sample training and testing (nonequivalence controls). The 2 remaining subjects (7 and 8) were exposed to matching-to-sample training and testing that incorporated stimuli not used during the transfer test; C1 and C2 were replaced by N1 and N2 during the matching-to-sample training and testing, but C1 and C2 were used for the transfer tests (equivalence controls). All 4 subjects failed to produce the self-discrimination transfer performances observed with the experimental subjects.     

ELECTROPHYSIOLOGICAL CORRELATES OF STIMULUS EQUIVALENCE PROCESSES

Research reported here concerns neural processes relating to stimulus equivalence class formation. In Experiment 1, two types of word pairs were presented successively to normally capable adults. In one type, the words had related usage in English (e.g., uncle, aunt). In the other, the two words were not typically related in their usage (e.g., wrist, corn). For pairs of both types, event‐related cortical potentials were recorded during and immediately after the presentation of the second word. The obtained waveforms differentiated these two types of pairs. For the unrelated pairs, the waveforms were significantly more negative about 400 ms after the second word was presented, thus replicating the “N400” phenomenon of the cognitive neuroscience literature. In addition, there was a strong positive‐tending wave form difference post‐stimulus presentation (peaked at about 500 ms) that also differentiated the unrelated from related stimulus pairs. In Experiment 2, the procedures were extended to study arbitrary stimulus—stimulus relations established via matching‐to‐sample training. Participants were experimentally näive adults. Sample stimuli (Set A) were trigrams, and comparison stimuli (Sets B, C, D, E, and F) were nonrepresentative forms. Behavioral tests evaluated potentially emergent equivalence relations (i.e., BD, DF, CE, etc.). All participants exhibited classes consistent with the arbitrary matching training. They were also exposed also to an event‐related potential procedure like that used in Experiment 1. Some received the ERP procedure before equivalence tests and some after. Only those participants who received ERP procedures after equivalence tests exhibited robust N400 differentiation initially. The positivity observed in Experiment 1 was absent for all participants. These results support speculations that equivalence tests may provide contextual support for the formation of equivalence classes including those that emerge gradually during testing.     

Class-consistent Differential Reinforcement And Stimulus Class Formation In Pigeons

Match-to-sample training clusters of A1 (sample): B1/B2 (comparisons), A2: B2/B1, B1: A1/A2, B2: A2/A1, B1: C1/C2, B2: C2/C1, C1: B1/B2, and C2: B2/B1 were presented to pigeons with class-consistent differential reinforcement using two dissimilar types of food reinforcers. Distinctive class-consistent response patterns occurred to the samples during the fixed-ratio 5 sample observing response requirement. Subsequent tests, modeled from the equivalence class paradigm demonstrated the emergence (80% class consistent) of the transitive-like A-C and C-A relations for 4 and 2 of 12 pigeons, respectively, and a strong trend (over 70%) for 7 and 6 others, respectively; the emergence of the reflexive-like identity relation when the nonidentical comparison was from the other class; and the disruption of the trained within-class relation with the addition of a reflexive comparison. After directional training of C1: D1/D2 and C2: D2/D1, tests indicated no emergence of the symmetric-like D-C relation or the composite D-B and D-A relations, but the B-D and A-D transitive-like relation occurred with some pigeons. Off-baseline training with class-consistent differential reinforcement contingent on responding to the D stimuli alone produced distinctive responding and, in turn, a trend to D-C symmetric-like control in 4 of 12 pigeons, as well as a shift toward class-consistent control on D-B and D-A test trials. Class-consistent differential reinforcement that produced distinctive sample behavior promoted stimulus control relations like those that circumscribe equivalence class formation. Respondent—operant interactions permit an analysis of the possible enrollment of stimulus values of distinctive responding to the discriminative stimuli forming the stimulus classes via processes corresponding to naming in humans.     

The effect of overlearning on transfer of training

The effect of overlearning on transfer of training on the A-B:A-B_r paradigm was studied in paired-associate learning with meaningful material (adjective pairs). One group of subjects was trained to criterion on list A-B, and two additional groups were given 100 per cent and 200 per cent overlearning on list A-B. Rate of learning list A-B_r was found to be directly related to amount of overlearning. Negative transfer on list A-B_r was found for errors with the criterion group, while positive transfer was found for the 100 per cent and 200 per cent overlearning groups. The results were consistent with previous paired-associate experiments, and with results of some maze, reversal learning experiments with infrahuman subjects.

The notation “A-B:A-B_r” will be used for the transfer paradigm in which the same stimuli and responses are used in both the original acquisition phase of paired associate learning and in the subsequent transfer of training phase. In the transfer phase, however, the responses (i.e. B) are rearranged so that they are paired with different stimuli (i.e. A). The notation “A-B:A-C” will be used for the transfer paradigm in which a new set of responses (i.e. C) are paired with the old set of stimuli in the transfer of training phase.     

Emergent equivalence relations between interoceptive (drug) and exteroceptive (visual) stimuli.

Conditional "if-then" relations between drug (interoceptive) stimuli and visual (exteroceptive) stimuli were taught to 4 normal humans. Interoceptive stimuli were the effects produced by 0.32 mg/70 kg triazolam (a prototypical benzodiazepine) and placebo (lactose-filled capsules); exteroceptive stimuli were black symbols on white flash cards. Following the training of the prerequisite conditional relations, tests of emergent relations were conducted between exteroceptive stimuli and between interoceptive and exteroceptive stimuli. Equivalence relations emerged immediately without explicit training for all 4 subjects. Accuracy of responding during the interoceptive-exteroceptive equivalence tests and subjects' self-reports showed consistent discrimination between the drug effects of triazolam and placebo. Finally, a generalization test assessed whether a novel visual stimulus presented in the context of the placebo (i.e., no drug) would generalize to visual stimuli belonging to the placebo stimulus class. All 3 subjects who completed this test reliably chose the visual stimuli belonging to the placebo class and not the visual stimuli belonging to the triazolam stimulus class. The development of equivalence relations between interoceptive and exteroceptive stimuli demonstrates that private and public stimulus events can emerge as members of the same equivalence class. Theoretical and clinical implications are discussed.