Multidimensional stimulus identification

In an absolute judgment task, total information transmitted about a set of stimuli increases as the dimensionality of the stimuli is increased. However, as the number of dimensions is increased, information transmitted about each component dimension decreases. Four factors were proposed that might, singly or in combination, account for this decrement: stimulus duration, interdimensional interference, distraction, and response complexity. The results of four experiments established that each of these factors may be operative under appropriate circumstances. It was also concluded that component dimensions were processed simultaneously rather than sequentially. However, the processing was not truly parallel because the input channels were not independent of one another.     

Dimensional stimulus control following brief wavelength training

Pigeons with extensive training pecking a key illuminated by a white line then had brief training with the key illuminated by 555 nanometers. This was immediately followed by a wavelength generalization test in extinction. Dimensional stimulus control about the training wavelength increased with the duration and number of reinforcements given on variable-interval 30-sec and variable-interval 10-sec schedules in Experiment I. In Experiment II, dimensional stimulus control was obtained after only 4 min of wavelength training from birds with prior and independent discrimination training. Experiment III provided groups equated in number of reinforcers with groups in Experiment I and two 8-min duration groups. Analyses, which included results from both Experiments I and III, showed that dimensional stimulus control increased: (a) more rapidly as a function of the duration of variable-interval 10-sec than variable-interval 30-sec reinforcement; (b) at the same rate across variable-interval reinforcement schedules, as a function of the number of reinforcers available during brief wavelength training.     

Drug discrimination: stimulus control during repeated testing in extinction

Rats were trained, under a two-lever drug-discrimination procedure, to respond differentially depending upon whether lorazepam (1.0 mg/kg) or no injection had been administered before the session. Responses on the appropriate lever produced a food pellet under a modified fixed-ratio (FR) 10 schedule, in which the 10 responses had to be emitted consecutively. In reinforcement tests, completing an FR 10 on either lever produced a pellet. In extinction tests, stimulus changes paired with reinforcement occurred but no pellet was delivered. Training sessions were conducted between test sessions. Each of four extinction phases consisted of six tests preceded by one stimulus (e.g., lorazepam). Repeated exposures to extinction reduced response rates for all rats, but stimulus control, as inferred from either percentage of total responses or percentage of total FR 10s on the drug-appropriate lever, remained high. The percentage of total FR 10s measure was less subject to skewing under low-rate conditions than was the percentage of total responses measure and provided an evaluation of stimulus control in terms of meeting the consecutive response contingency. These results demonstrate a level of independence between response rate and stimulus control in drug discrimination, which has positive implications for the validity of interpreting discriminative effects of novel test conditions in well-trained animals, even when overall response rates are low.     

Behavioral control by an imprinted stimulus: long-term effects

Newly hatched ducklings were exposed to imprinting procedures and subsequently trained to peck a key by presenting the imprinting stimulus as the reinforcing (response-contingent) event. Individual ducklings then lived in the apparatus under an arrangement in which each peck produced a 15-sec stimulus presentation. For all ducklings, key-pecks tended to occur in bursts, and as the duckling matured, burst length decreased and the interval between bursts increased. However, even when subjects were 60 days old, some responses still occurred.     

Multidimensional adaptive testing

Maximum likelihood and Bayesian procedures for item selection and scoring of multidimensional adaptive tests are presented. A demonstration using simulated response data illustrates that multidimensional adaptive testing (MAT) can provide equal or higher reliabilities with about one-third fewer items than are required by one-dimensional adaptive testing (OAT). Furthermore, holding test-length constant across the MAT and OAT approaches, substantial improvements in reliability can be obtained from multidimensional assessment. A number of issues relating to the operational use of multidimensional adaptive testing are discussed.     

Factors influencing inhibitory stimulus control: discrimination training and prior non-differential reinforcement

In Exp. I, shallow U-shaped gradients of inhibition in the line-orientation dimension were obtained from birds that had a vertical (0°) line on a green surround correlated with extinction and a blank green surround correlated with reinforcement. Birds that had massed extinction in the presence of the 0° line showed flat gradients. Thus, discrimination training, but not massed extinction, appears to generate inhibitory control. In Exp. II, as in studies of control by a stimulus correlated with punishment, non-differential training across the line-orientation dimension preceded further sessions. Steep inverted gradients about the 0° line were obtained after discrimination training with the 0° line correlated with extinction. Gradients obtained after massed extinction tended to be flat. Again, discrimination training was critical in obtaining negative gradients of stimulus control.     

Effects of extradimensional discrimination training upon previously acquired stimulus control

In Experiment 1, three groups of pigeons were taught to discriminate vertical lines (positive) from horizontal (negative). One group was then given true-discrimination training between two colors, a second group was equally reinforced for responding to the colors (pseudodiscrimination), while the third group was not run. The pseudodiscrimination group then provided a flatter gradient on the dimension of line orientation than either of the others, which did not differ. A second experiment demonstrated that this flattening effect could be completely counteracted when pseudodiscrimination was followed by true discrimination before the generalization test. The results are discussed within the framework of current research on attentional factors governing generalization gradients; pseudodiscrimination affects tests of stimulus control rather than its acquisition. When it intervenes between acquisition and testing, it appears to produce a “lapse” rather than a “loss” of the memory of the first-trained stimuli.     

Incongruous stimulus pairing and conditional discrimination training: effects on relational responding

In Experiment 1, 5 subjects were exposed to a stimulus-pairing procedure in which two nonsense syllables, identified by a letter-number code as A1 and C2, each predicted the onset of a sexual film clip, and the nonsense syllables A2 and C1 each predicted the onset of a nonsexual film clip. Subjects were then exposed to a matching-to-sample test in which the nonsense syllables A1 and A2 were presented as sample stimuli and C1 and C2 were presented as comparison stimuli and vice versa (i.e., C stimuli as samples and A stimuli as comparisons). All subjects matched A1 with C2 and A2 with C1. Subjects were then trained on the conditional discriminations A1-B1, A2-B2, B1-C1, B2-C2, after which the matching-to-sample test was again administered. All subjects continued to match A1 with C2 and A2 with C1 in accordance with the earlier stimulus-pairing contingencies. An additional 5 subjects were exposed first to conditional discrimination training and testing before being exposed to the incongruous stimulus pairing and matching-to-sample testing. Under these conditions, 4 of the 5 subjects always matched A1 with C1 and A2 with C2. Experiment 2 replicated Experiment 1, except that a matching-to-sample test was not administered following the initial training procedure. Under these conditions, matching-to-sample test performances were controlled by the contingencies that had immediately preceded the test. Experiment 3 indicated that initial matching-to-sample test performances were unlikely to change, even after repeated exposure to incongruous training and testing. Experiment 4 demonstrated that pretraining with unrelated stimulus sets increased the sensitivity of matching-to-sample test performances to incongruous contingencies when they were similar in format to those arranged during pretraining. These data may have implications for a behavior-analytic interpretation of attitude formation and change.     

Factors influencing inhibitory stimulus control: differential reinforcement of other behavior during discrimination training

Pigeons were trained to respond on a multiple variable-interval 1-min variable-interval 1-min schedule, then switched to a multiple variable-interval 1-min differential-reinforcement-of-other-behavior discrimination training. The rate of reinforcement was held constant during the shift from non-differential reinforcement to discrimination training. Behavioral contrast and post-discrimination inhibitory stimulus control followed the observation of a reduction in the rate of responding to the stimulus correlated with reinforcement for the non-occurrence of pecking.     

Comparison of stimulus control and reinforcement control effects on imitative behavior

An attempt was made to evaluate reinforcement and stimulus control of imitative and non-imitative behavior. The imitative response required the subject to duplicate the experimenter's response by matching blocks that varied in color. The factor designed to evaluate stimulus control was fading, a procedure that systematically varies the differences between the imitative and non-imitative stimuli. The topography and duration of the non-imitative stimuli were faded in. The factors designed to evaluate reinforcement control were differential reinforcement of non-imitative behavior and time out from positive reinforcement. The results showed stimulus control of non-imitation to be more important than reinforcement control, and that reinforcing events were not sufficient to control non-imitation; while the arrangement of stimulus events was sufficient to control non-imitation. These results were related to studies providing evidence for the processes of discrimination and generalization.     

Evidence of interaction between deprivation effects and stimulus control

Discriminative responding in pigeons was studied under multiple variable-interval extinction and variable-ratio extinction schedules, as deprivation was varied. Generally, the greater the accuracy of discrimination that developed during training, the smaller the effect of deprivation upon subsequent performance. This was true both in terms of changes in response rates, and in the relationship between response rates during food reinforcement and extinction. When discrimination was inaccurate, increases in deprivation resulted in disproportionate increases in responding during extinction, as compared to increases during food reinforcement components of the schedule. The results suggest that as stimulus control (accuracy) of responding increases, discriminative performance becomes less and less susceptible to influence by deprivation.     

Behavioral contrast and inhibitory stimulus control as related to extended training

Pigeons received discrimination training in which the presence of a white field was correlated with variable-interval reinforcement and the presence of a monochromatic field was correlated with extinction. Responses during the negative stimulus prolonged its duration. Five experimental groups each received a different number of discrimination sessions up to 70 sessions. The last session was followed by a wavelength generalization test. The control group was tested both before and after four discrimination sessions. Responding to the positive training stimulus was enhanced in all groups by the discrimination procedures. This enhancement tended to decrease over sessions in some animals but it never disappeared in others. Responding to the test stimuli preceding discrimination training was minimal around the negative stimulus and increased in either direction away from that wavelength. Responding to the test stimuli was not systematically related to the amount of discrimination training.     

Repeated measurements of reinforcement effects on gradients of stimulus control

Two experiments studied the effects of reinforcement schedules on generalization gradients. In Exp. 1, after pigeons' responding to a vertical line was reinforced, the pigeons were tested with 10 lines differing in orientation. Reconditioning and the redetermination of generalization gradients were repeated from 8 to 11 times with the schedule of reinforcement varied in the reconditioning phase. Stable gradients could not be observed because the successive reconditionings and tests steepened the gradients and reduced responding. Experiment 2 over-came these effects by first training the birds to respond to all of the stimuli. Then, brief periods of reinforced responding to the stimulus correlated with reinforcement alternated with the presentation of the 10 lines in extinction. The development of stimulus control was studied eight times with each bird, twice with each of four schedules of reinforcement. Gradients were similar each time a schedule was imposed; the degree of control by the stimulus correlated with reinforcement varied with particular schedules. Behavioral contrast occurred when periods of reinforcement and extinction alternated and was more durable with fixed-interval, variable-interval, and variable-ratio schedules than with fixed-ratio or differential-reinforcement-of-low-rate schedules.     

Discriminative stimulus control and the effects of concurrent operants.

Discriminative-stimulus-control functions were investigated in a concurrent operant context. Variable-interval reinforcement schedules were arranged for pigeons on two response keys. One key, illuminated with a white vertical line on green background (position irrelevant), was programmed with a given schedule value across groups. For different groups of pigeons, the alternative key, illuminated with green alone, was programmed with twice, the same, or half the reinforcement frequency of the other key. Stimulus-control gradients were collected from both keys as line orientation was varied. On the green-plus-line alternative, flattest gradients were observed when twice the reinforcement frequency was concurrently programmed and the steepest were observed when equal values were concurrently programmed. Also examined were the effects of a programmed changeover delay, important in maintaining the independence of concurrent operants. The changeover delay was found to have relatively minor effects upon stimulus control, despite its typical and marked effects upon steady-state responding.     

Manipulating establishing operations to verify and establish stimulus control during mand training

Acquisition of verbal behavior is a major goal of interventions for children with developmental disabilities. We evaluated the effectiveness of manipulation of an establishing operation for functional discriminated mands. Four individuals with developmental disabilities participated in a training procedure designed to teach two separate mands for two separate preferred items. Participants were taught to mand using picture cards. Following training, the manipulation of the establishing operation was used to assess and establish discriminated manding. This manipulation involved providing free access to one of the preferred items, such that there should be no motivation to ask for it, while motivation to ask for the other item remained in place. Three of the 4 participants acquired discriminated manding using topographically similar responses (picture cards). One participant did not acquire a discriminated mand until topographically distinct mands were taught (vocal and picture card). Results suggest that discrimination training is not necessarily sufficient to teach discriminated manding when more than one picture card showing preferred items is used. In addition, manipulation of the establishing operation served as an appropriate assessment tool for the verification of discriminated manding as well as a possible training tool to establish discriminated manding.     

Context-specific prime-congruency effects: On the role of conscious stimulus representations for cognitive control

Recent research suggests that processing of irrelevant information can be modulated in a rapid online fashion by contextual information in the task environment depending on the usefulness of that information in different contexts. Congruency effects evoked by irrelevant stimulus attributes are smaller in contexts with high proportions of incongruent trials and larger in contexts with high proportions of congruent trials (e.g., Corballis and Gratton, 2003, Lehle and Hübner, 2008). The present study investigates these context-adaptation effects in a masked-priming paradigm. Context-specific adaptation effects transfer to stimulus identities that are equiprobale in all contexts – an observation that renders explanations in terms of event-learning processes unlikely. Yet, context-specific effects vanished when the irrelevant information remained unconscious. The results suggest that context-specific adaptation of congruency effects reflect cognitive control operations that alter the processing of irrelevant information depending on the experienced utility of that information for action control.     

Sample stimulus control shaping and restricted stimulus control in capuchin monkeys: a methodological note

This paper reports use of sample stimulus control shaping procedures to teach arbitrary matching-to-sample to 2 capuchin monkeys (Cebus apella). The procedures started with identity matching-to-sample. During shaping, stimulus features of the sample were altered gradually, rendering samples and comparisons increasingly physically dissimilar. The objective was to transform identity matching into arbitrary matching (i.e., matching not based on common physical features of the sample and comparison stimuli). Experiment 1 used a two-comparison procedure. The shaping procedure was ultimately effective, but occasional high error rates at certain program steps inspired a follow-up study. Experiment 2 used the same basic approach, but with a three-comparison matching task. During shaping, the monkey performed accurately until the final steps of the program. Subsequent experimentation tested the hypothesis that the decrease in accuracy was due to restricted stimulus control by sample stimulus features that had not yet been changed in the shaping program. Results were consistent with this hypothesis, thus suggesting a new approach that may transform the sample stimulus control shaping procedure from a sometimes useful laboratory tool to a more general approach to teaching the first instance of arbitrary matching performances to participants who show protracted difficulties in learning such performances.