Interference effects on preschool children's learning sets

Four experiments investigated interference in 5-year-olds' learning sets. Experiment 1 manipulated intertrial and interproblem intervals, showing that increased intertrial intervals retarded performance. Long interproblem intervals interacted with short intertrial intervals to produce performance facilitation. Experiment 2 investigated interpolations within problems with either similar or dissimilar stimulus presentations. Similar stimuli caused greater performance decrements than dissimilar. Experiment 3 hypothesized that the within-subjects design of Experiment 1 masked interproblem interval effects. Testing between-subjects established that increased interproblem delays facilitate performance. In Experiment 4 interproblem delays were further tested in a series of shifts within and between dimensions. Increased delays more greatly benefited shifts within dimensions. It is concluded that intertrial and interproblem intervals affect learning set performance differentially. Intertrial delays result in performance deterioration due in part to interference. Interproblem delays facilitate performance at least in part by providing the opportunity for suppression of proactive interference, and perhaps in part by providing the opportunity for constructive cognitive processing.     

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.     

A developmental study of differences in initial coding and recoding of hypothesis information

Coding and recoding of hypothesis information was studied in children in Grades 3, 5, and 7, and college students. Each S was tested on several two-choice discrimination problems. A problem consisted of two trials, a training trial and a test trial. The information available for coding on the first trial was varied in three series of problems by using pairs of stimuli differing in 3, 4, or 6 dimensions. Recoding after an error was facilitated in half of the problems in each series by allowing the stimuli to persist briefly after response and feedback. The stimuli terminated immediately after response and feedback in the remaining problems. The second trial of a problem, in which the stimuli differed on only one dimension, was used to probe for the information coded or recoded on the first trial. On the average, fewer dimensions were coded per trial by the younger Ss than by the older Ss. Neither the effects of negative feedback nor the effects of stimulus persistence were found to be related to developmental level. It was concluded that a deficiency in young children's ability to code, but not recode, hypothesis information contributes to their less efficient performance in discrimination problems.     

Controlling relations in conditional discrimination and matching by exclusion.

Normally capable adults learned two-choice identity matching of three-digit numerals and arbitrary matching of physically dissimilar nonsense syllables. The stimuli were displayed on a computer terminal, and responses consisted of typing on the terminal's keyboard. In Experiment 1, every trial displayed a sample numeral, a comparison numeral, and three equal signs (= = =). The comparison stimulus was to be selected if it was identical with the sample; otherwise the equal sign was to be selected. This "single comparison" method was then used to show that arbitrary matching could be based upon either sample-S+ or sample-S- relations. In Experiment 2, a series of probe trials displayed a novel sample, a comparison stimulus from the arbitrary matching baseline, and = = =. Subjects typically selected = = =; they apparently were excluding the baseline comparison stimulus. Experiments 3 through 5 investigated which variables in training would lead to the selection of baseline comparison stimuli in response to novel samples. Behavior was usually unchanged when baseline training included relating comparison stimuli to as many as four different samples. Punishment contingencies were effective, but performance did not generalize unless those contingencies were applied in relation to more than one baseline comparison stimulus.     

Assessment of the relative importance of S+ and S− in rats using differential training on intercurrent discriminations

The present studies assessed the degree of stimulus control exerted by S+ and S? without confoundings of stimulus novelty and stimulus ambiguity. In Experiment 1, rats were trained on two intercurrent simultaneous discrimination problems with nine times more training given on one than the other. Then the animals were given transfer tests with re-paired stimuli. The results showed that S? exerts greater stimulus control than S+ in a two-choice simultaneous discrimination. Experiment 2 provided a test of the possibility that the relative degree of control by S? varies with different amounts of training. Three groups were trained on two intercurrent simultaneous discrimination problems; each group was given 7, 11, or 15 times more training on one problem than the other. Then transfer tests were given with re-paired stimuli. Again the results showed that S? exerts greater stimulus control than S+ in a two-choice simultaneous discrimination.     

The ambiguous-cue problem: The effects of reduced similarity between trials and the schedule of reinforcement

In a series of seven experiments pigeons were trained on the two-choice ambiguous-cue problem that contains PA and NA trials. On PA trials choice of P (the positive stimulus) was reinforced and choice of A (the so-called ambiguous stimulus) was not reinforced; on NA trials choice of A was reinforced and choice of N (the negative stimulus) was not reinforced. When the two types of trials were distinguished by only the presence of P or N and each trial was terminated by one response, subjects quickly attained high levels of performance on NA trials but showed only chance levels of performance on PA trials. PA performance was markedly improved when a variety of additional stimuli distinguished the two types of trials and when a variety of schedules of intermittent reinforcement were employed; these manipulations had little effect on NA performance.     

Ambiguous-cue learning in preschool children: A test of the dimensional characteristics of task stimuli

Sixteen preschool children were administered a two-choice discrimination problem consisting of three stimulus compounds: the consistently rewarded stimulus, the consistently nonrewarded stimulus, and the ambiguous stimulus which was nonrewarded when paired with the positive, but rewarded when paired with the negative. When both pair of stimuli, positive-ambiguous and negative-ambiguous, were presented together the subject was required either to choose or to avoid the ambiguous stimulus depending upon the stimulus with which it was paired. In Experiment 1, when each of three stimuli (positive, negative, ambiguous) varied along one nonspatial cue dimension (color), performance was better on negative-ambiguous trials than positive-ambiguous trials. In Experiment 2, when the positive and negative stimuli varied along three nonspatial cue dimensions (colors and form) and the ambiguous stimulus varied along one of these dimensions (color), superior positive-ambiguous over negative-ambiguous performance was obtained. These findings complement those reported for other subjects and confirm Berch's (D. B. Berch, Learning and Motivation, 1974, 5, 135–148) predictions regarding use of differential numbers of cue dimensions.     

Responding in configural discrimination problems depends on density of reinforcement in time

Previous research has shown that conditioned responding in differential skin conductance conditioning increased for reinforced stimuli (CSs+) but remained constant for nonreinforced stimuli (CSs-) due to decreasing reinforcement density. The present two experiments (Experiment 1: Negative patterning; Experiment 2: Positive patterning) were designed to disentangle a possible confound of reinforcement density with stimulus frequency. In order to achieve this, we varied the intertrial interval (18 s, 24 s, or 48 s) and held constant the numbers of CSs+ and of CSs- in each of both discrimination problems. With increasing intertrial intervals, we found higher responding both to CSs+ and to CSs- as well as increased response differentiation. We discuss these results with respect to two mechanisms offered by Wagner's SOP model and conclude that the observed effects are due to variations in density of reinforcement in time.     

Peripheral visual processing

An attempt was made to examine the development of the ability to identify stimuli presented to peripheral vision in several different tasks. Five- and 8-year-old children and college adults saw, for 20 msec, either a single figure at 1°, 2°, 4°, or 6° of visual angle from the fovea (singleform condition) or an off-foveal figure with an additional figure at the fovea (double-form condition). In the double-form conditions, the subjects were required to identify either the peripheral figure only (double-form presentation) or both figures (double-form report). The main effects of Age, Distance, and Form Condition were significant. Accuracy improved with increasing age and with decreasing distance. The Form Condition effect reflected lower accuracy in the two double-form conditions than in the single-form condition. Interestingly, there was no difference between the two double-form conditions, suggesting that the mere presence of a foveal stimulus, with instructions to ignore it, produces as much decrement in peripheral performance as when subjects are told to fully process and report the foveal stimulus. Also, there was no interaction between Form Condition and Distance, suggesting that the label “tunnel vision” may be misleading, since the presence of the foveal stimulus seems to have an equal effect on all peripheral locations and does not really “restrict” the size of the effective visual field.     

A model for response tendency combination

A model is proposed to predict the performance on a compound stimulus as a function of the performance on the component stimuli in a two-choice situation. Data from a learning task are used to evaluate the model.The initial work on the model was carried out under the Summer Faculty Research Fellowship Program of the Horace H. Rackham School of Graduate Studies at the University of Michigan. Acknowledgment is also due Mr. Richard Anderson for his assistance in data collection.     

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.     

Response summation to a compound stimulus in a context of choice

Key pecks by two groups of pigeons were reinforced on concurrent schedules. For group Ē, pecks were reinforced during either a visual or an auditory stimulus; for group E, an additional, extinction component was available, during which both visual and auditory stimuli were absent. After training, both groups were given a compound test to measure preference among four stimuli, the three used in training plus a compound of the visual and auditory stimulus. Group E showed preference for the compound, emitting more pecks and spending more time in this stimulus than in other stimuli. Group Ē showed no preference between the compound and visual stimulus, nor between the auditory stimulus and the absence of both stimuli, but preferred the former pair over the latter pair of stimuli.     

An analysis of emergent simple discrimination in children

In Experiment 1 eight five-year-old children received an arbitrary matching-to-sample task with sample stimuli A1 and A2 and comparison stimuli B1 and B2. This task was mixed with a simple, two-choice discrimination task with stimuli A1 and A2. In subsequent tests with B1 and B2 presented alone, the number of responses to B1 was greater when it had been paired with the correct stimulus of the simple discrimination task than when it had been paired with the incorrect stimulus. In Experiment 2 incorrect comparisons were omitted during the matching-to-sample task. Eight children were taught to point to either A1 or A2 first, and to either B1 or B2 second. Eight other children were taught to point to either B1 or B2 first, and to either A1 or A2 second. The effect of Experiment 1 was replicated with the first but not with the second group. The results of both experiments suggest that the functions of S+ and S- in a simple discrimination task can transfer to test stimuli if the training stimuli precede the test stimuli during paired presentations.     

Sensory Processing Sensitivity and its association with personality traits and affect: A meta-analysis

In two Bayesian meta-analyses, we investigated associations between Sensory Processing Sensitivity (SPS) and the Big Five personality traits (MA1) as well as both Positive and Negative Affect (MA2). Moderators were age and the three SPS subscales. In MA1 (8 papers, 6790 subjects), SPS in children correlated with Neuroticism (r = 0.42) but did not with Extraversion, Openness, Agreeableness or Conscientiousness. In adults, SPS correlated with Openness (r = 0.14) and Neuroticism (r = 0.40) but did not with Extraversion, Agreeableness or Conscientiousness. In MA2 (19 papers, 5326 subjects), SPS in children correlated with Negative (r = 0.29) and Positive Affect (r = 0.21), but only with Negative Affect (r = 0.34) in adults. Developmental and measurement aspects are discussed.     

Developmental changes in attentional skills: the effect of irrelevant variations on encoding and response selection

The present experiments examine how irrelevant variations within a stimulus set interfere with performance in a selective attention task. Second graders, fifth graders, and adults were administered a discrete trial version of a selective attention task in which they were required to search for an object that matched the prime on the targeted dimension. The stimuli in the first experiment were constructed from spatially integrated dimensions whereas the second experiment used spatially separated dimensions. The results indicated that while the spatially separated dimensions were perceived independently by all age groups, developmental differences in perceived structure were evident with the spatially integrated dimensions. Problems associated with response selection were a major source of interference with both types of stimuli, but the severity of the interference varied with the age of the perceiver and the nature of the stimuli. The developmental implications of these findings were considered.     

The time course of task switching: A speed—accuracy trade-off analysis

On each trial of this study, participants either switched between or repeated two simple, two-choice tasks involving either letter or digit classifications. Speed-accuracy trade-off (SAT) curves were obtained using the responsesignal method of eliciting speeded responses at various response time lags after the presentation of the stimulus for the second task. The key finding from separate analyses of the three SAT-curve parameters (intercept, rate, and asymp tote) was that the location of the intercept of the SAT function (i.e., the point at which responding rises above chance) was shifted upward for both short and long response-stimulus intervals under task-switch conditions but only when the responses associated with each of the letter-digit stimulus components were incompatible.     

Keeping Simon simple: Examining the relationship between sequential modulations and feature repetitions with two stimuli, two locations and two responses

The present study examined performance across three two-choice tasks that used the same two stimuli, the same two stimulus locations, and the same two responses to determine how task demands can alter the Simon Effect, its distribution across reaction time, and its sequential modulation. In two of the tasks, repetitions of stimulus features were not confounded with sequences of congruent and incongruent trials. This attribute allowed us to investigate the sequential modulation of the Simon Effect in a two-choice task while equalizing the occurrence of feature repetitions. All tasks showed a similar sequential modulation, suggesting that it is not driven by feature repetitions. Moreover, distributional analyses revealed that the advantage for congruent trials decreased as reaction time increased similarly following congruent and incongruent trials. Finally, a large increase in RT was observed when repeated responses were made to novel stimuli and when novel responses were made to repeated stimuli. This effect also showed a sequential modulation regardless of whether the stimulus repeated. The findings suggest that, even in two-choice tasks, response selection is mediated by complex, dynamic representations that encode abstract properties of the task rather than just simple features.     

An analysis of the solution of PAN ambiguous-cue problems by rhesus monkeys

Twenty-four monkeys were given 2-choice discrimination problems composed of three planometric plaque stimuli: P, the rewarded stimulus; N, the nonrewarded stimulus; and A, the ambiguous stimulus which was negative when paired with P, but positive when paired with N. When both pair of stimuli, PA and NA, were presented within a given session S was forced either to approach or to avoid the A plaque depending upon the stimulus with which it was paired. The results corroborated previous reports for plaque stimuli by showing PA performance to be superior to NA. The data also revealed that when plaque stimuli with distinctive cues were employed, NA performance exceeded PA as previously reported for stereometric object stimuli. Pretraining Ss with plaque stimuli possessing distinctive cues, then switching to plaques with less distinctive cues, also resulted in superior NA performance. These findings are discussed in the context of an interference-cue theory.     

Effects of neutral and positive stimuli on stuttering: “Calling attention to stuttering” revisited

This study investigated the effects of presumably positive and neutral response-contingent stimuli on the occurence of stuttering. Eight adult stutterers spoke spontaneously during a 60-min experimental session, which was divided into three 20-min periods. During Condition I no stimuli were delivered. During Condition II a digital counter and a pair of yellow lights were activated each time the subject stuttered. During Condition III these same response-contingent stimuli were delivered, but with the additional factor that the subject would earn 5¢ each time the counter moved forward and the lights were illuminated. Conditions II and III were counterbalanced across subjects. The experimenter was unaware of which of the two contingencies were operative during Conditions II and III. Results showed no significant changes in occurence of stuttering due to either response-contingent stimulus. A discussion of theoretical and experimental implications is given.     

Negative priming depends on ease of selection

Negative priming effects have been offered as evidence that distractor stimuli are identified. We conducted two experiments to determine if such effects occur even when it is easy to discriminate target from distractor stimuli. In Experiment 1, we found the usual negative priming effect when target and distractor positions varied from trial to trial, but not when these positions remained fixed. Experiment 2 extended these results to a situation where the ease of selection varied only in the prime display. These findings argue that irrelevant inputs can be filtered out prior to stimulus identification under certain circumstances and therefore pose problems for strict late selection theories.