Temporal parameters of the feature positive effect

Trial duration and intertrial interval duration were parametrically varied between groups of pigeons exposed to a discrimination involving the presence vs. the absence of a dot. Half the groups received the dot as the positive stimulus (feature positive groups) and half the groups received the dot as the negative stimulus (feature negative groups). Faster learning by the feature positive birds (feature positive effect) was found when the trial duration was short (5 sec) regardless of whether the intertrial interval was short (5 sec) or long (30 sec). No evidence for a feature positive effect was found when the trial duration was long (30 sec) regardless of the length of the intertrial interval (30 sec or 180 sec). The results suggest that short trial duration is a necessary condition for the occurrence of the feature positive effect, and neither intertrial interval nor trial duration/intertrial interval ratio are important for its occurrence. The suggestion that mechanisms underlying the feature positive effect and autoshaping might be similar was not supported by the present experiment since the trial duration/intertrial interval ration parameter appears to play an important role in autoshaping but not the feature positive effect.     

Optimal Stimulus Parameters In Avoidance Conditioning Of Inbred Strains Of Mice

Highly inbred mice of fast and slow conditioning strains (N = 228) were trained in avoidance conditioning and 180 were continued to extinction. The principal goal was to determine optimal stimulus conditions for fast learning, small variances, and maximal strain differences. Conclusions are: a) the major effect of change in CS-US and intertrial intervals occurs, respectively, for intervals less than 3 sec. and 60 sec.; b) change in amperage (150-400 pa) or voltage (250-400 v.) caused no significant differences; c) strain differences in extinction occurred after nearly optimal conditioning, and d) strain differences were altered considerably as stimulus conditions became optimal. Optimal levels of parameters are: 3 sec. CS-US interval, 120-sec. intertrial interval, and 400 v. (220 K ohm impedance circuit).     

Function of intertrial interval in matching-to-sample

Twelve pigeons were trained on matching-to-sample using either a 0-, 5-, 15-, 25-, or 60-sec intertrial interval. Eight of these 12 pigeons were given one of the following intertrial interval changes: 0 to 60, 0 to 5, 5 to 0, 60 to 0, 15 to 25, 5 to 15, 60 to 5, 5 to 1, 1 to 5, 1 to 25, and 25 to 1 sec. Most intertrial interval changes were repeated at least once. The 0-sec intertrial interval subjects failed to match beyond chance levels, while other intertrial interval values resulted in matching acquisition. Changes from 0 sec to other intertrial interval values increased and changes to 0 sec decreased matching performance. Changes to intertrial interval values other than 0 sec resulted in little change in matching accuracy once stable performance had been attained.     

The Effects of Hippocampal and Area Parahippocampalis Lesions in Pigeons: I. Delayed Matching to Sample

Four experiments were conducted to determine the effects of bilateral damage to the hippocampus and area parahippocampalis (Hp-APH) on visual memory in pigeons using the delayed matching-to-sample (DMS) procedure. In Experiment 1, we generated visual retention gradients with delays of 0, 1.5, 3, 6, and 12 sec both preoperatively and postoperatively in three pigeons with considerable preoperative visual DMS experience. Bilateral Hp-APH lesions had no effect whatsoever on visual retention. In Experiment 2, we examined the effects of Hp-APH lesions on both the acquisition of a visual DMS task with a 0-sec delay, and the subsequent retention performance with delays of 0, 3, 6, 12, and 24 sec. There was no difference between unoperated control pigeons and Hp-APH pigeons either in terms of the number of sessions required to learn the visual DMS task or in terms of their subsequent visual retention performance levels. In Experiments 3 and 4, we examined whether Hp-APH pigeons might be more sensitive than control pigeons to the effects of proactive interference (by reducing the duration of the intertrial interval) and retroactive interference (by introducing delay-interval illumination). Although reducing the duration of the intertrial interval and increasing the level of delay-interval illumination both resulted in lower performance levels on the visual DMS task, there was no indication that the Hp-APH pigeons were any more affected by the changes in interference levels than were unoperated control pigeons. These findings support the view that the Hp-APH in pigeons plays little role in the processing and retention of purely visual information.     

Role of intertrial interval following an escape or avoidance response in bar-press avoidance

In three experiments, rats learned bar-press avoidance as a function of the intertrial interval following an escape or an avoidance. The general hypothesis is that the length of these intervals affects bar-press avoidance differentially, depending on whether an avoidance follows an escape (avoidance/escape) or an avoidance (avoidance/avoidance) on the previous trial. Specifically, it is proposed that short escape ITIs will facilitate avoidance/escape and avoidance/avoidance, while avoidance ITIs will have no effect on avoidance responding. The results tend to support this hypothesis. The shorter the intertrial interval following an escape, the higher the probability of both measures: avoidance/escape and avoidance/avoidance. No effect of avoidance interval was found on avoidance/avoidance. Unpredictedly, however, it was found that in comparison to a very short intertrial interval following an avoidance (0.5 sec), relatively long intervals (5 and 45 sec) facilitate avoidance/escape. These results were interpreted as mainly reflecting nonassociative factors such as shock-produced activity.     

Pavlovian conditioning of shock-elicited aggression: a discrimination procedure

Two auditory stimuli, separated by a fixed intertrial interval, were alternately presented to two rats in a closed environment. The positive conditioned stimulus (CS+) terminated with the offset of a 2-mA, 0.75-sec shock. The negative conditioned stimulus (CS-) terminated without shock. The incidence of the "stereotyped fighting posture" was recorded during the CS+, the CS-, the intertrial interval, and shock. The results showed an increase in the percentage of conditioned responses during the CS+, and a decrease during both the CS- and the intertrial interval, when the duration of the conditioned stimuli and the intertrial interval was 16 sec. Appropriate changes in the incidence of aggression during the two stimuli were obtained following the reversal of the stimulus functions. During the acquisition and reversal phases there was a between-session decrement and a within-session improvement in the incidence of aggression during the CS+, defined as warm-up. The presentation of free shocks before the conditioning sessions was effective in reducing the warm-up only when the interval between shocks was 64 sec. These data were interpreted as demonstrating classical conditioning of shock-elicited aggression, with little chance of non-associative factors contributing to the measurement of the conditioned response.     

Lateral preference for identical geometric forms: I. Normals

Ss made size discriminations between two identical and equal-sized geometric forms presented tachistoscopically. Under “larger” instructions the right side stimulus was chosen more often. Under “smaller” instructions and 30 sec. intertrial interval, the left side was chosen more often; with 10 sec. intertrial interval and “smaller” instructions perceptual and motor preferences canceled one another.     

The sex difference in rotary pursuit performance: aptitude or inhibition?

This study examined the hypothesis that male dominance in the acquisition and performance of rotary pursuit skill reflects a lower male proclivity for the generation and accumulation of reactive inhibition rather than some innately superior ability to profit from practice. On this hypothesis, the magnitude of male dominance should decline as the length of the intertrial interval increases. The experimental sample consisted of 120 Caucasian subjects (60 of each sex) who were given sixty 30-sec trials on rotary pursuit with intertrial intervals ranging from 0 to 40 sec. The principal finding was that the magnitude of the sex difference depended significantly upon the length of the intertrial interval, as hypothesized. When the interval was 10 sec or longer, performance levels of the sexes were essentially equal. The sex variance was reduced to insignificance even on the first trial when allowance was made for the inhibitory effect of practice. Thus, male dominance in rotary pursuit skill appears to be a procedural effect mediated by and inhibitory mechanism rather than a consequence of differential endowments of learning ability.     

The Sex Difference in Rotary Pursuit Performance

This study examined the hypothesis that male dominance in the acquisition and performance of rotary pursuit skill reflects a lower male proclivity for the generation and accumulation of reactive inhibition rather than some innately superior ability to profit from practice. On this hypothesis, the magnitude of male dominance should decline as the length of the intertrial interval increases. The experimental sample consisted of 120 Caucasian subjects (60 of each sex) who were given sixty 30-sec trials on rotary pursuit with intertrial intervals ranging from 0 to 40 sec. The principal finding was that the magnitude of the sex difference depended significantly upon the length of the intertrial interval, as hypothesized. When the interval was 10 sec or longer, performance levels of the sexes were essentially equal. The sex variance was reduced to insignificance even on the first trial when allowance was made for the inhibitory effect of practice. Thus, male dominance in rotary pursuit skill appears to be a procedural effect mediated by an inhibitory mechanism rather than a consequence of differential endowments of learning ability.     

Stimulus control of the pigeon's ability to peck a moving target.

Two pigeons were trained to peck whichever of eight keys displayed a white field (SD). The other seven keys displayed a white "X" on a black background (S delta). Each peck to SD produced three-second access to grain, a three-second intertrial interval (ITI), and the next trial. Pecks to S delta produced a three-second timeout (TO) and the same trial. During later sessions the key displaying SD changed every t seconds (t = 3, 2, 1, .5, and .25 sec), requiring the birds to track the position of the SD. Pecks on a ninth key increased t. Several sessions employed novel stimuli to ascertain the controlling stimulus dimensions. Both birds made few errors acquiring the original discrimination. During the tracking sessions, both birds made few errors when t = .5 sec. Only one reliably lengthened t. Data from sessions with novel stimuli indicate that color and form were important aspects of SD and S delta respectively; movement contributed to the final performance.     

Is reading ability related to activation dumping speed? Evidence from immediate repetition priming

In parallel processing models, residual activity constitutes noise that must be dumped, and fast dumping is associated with efficient processing. Subjects performed a continuous lexical decision task with repetitions (Experiments 1 and 2). Efficient readers (who had high comprehension and vocabulary scores) showed smaller repetition priming than did inefficient readers, but mostly at Lag 0 (equivalent to 3-sec stimulus onset asynchrony [SOA]). Experiment 3 manipulated the empty interrepetition interval. It was found that reading ability was negatively related to repetition priming mostly when the SOA was 3 sec, but less so when it was 2 or 4 sec. Experiment 4 failed to find similar reading ability differences when the task was continuous recognition. The findings are interpreted as showing that efficient readers managed to dump residual activity related to subsemantic information in less than 3 sec, whereas inefficient readers required 3–4 sec.     

The role of instrumental responding and contiguity of stimuli in the development of infant secondary reinforcement

Ten-month-old infants received contingent pairings of a tone (T+) and food reinforcer. Groups S^r and S^D received the food on an FI 23-sec schedule for target touching, the former group receiving T+ immediately after the response and 1.5 sec prior to food and the latter group receiving T+ at the end of the intertrial interval. Group SC received food reinforcers 1.5 sec after T+ with no response required. A second tone (Tⁿ) was heard by all groups once during each intertrial interval, at randomly determined points. All groups subsequently were given a spatial discrimination task, receiving T+ for one alternative and Tⁿ for the other. Group S^r gave significantly more responses for T+ than for Tⁿ, but neither of the other two groups produced a superiority for T+. Thus, both contiguity with a primary reinforcer and the presence of an operant during training appear to be necessary for a neutral signal to acquire the ability to enhance responding.     

Short-term memory for time intervals

The effect of intertrial interval, preset interval, and retention interval on the performance of rats in a time estimation task was described. On each trial a signal was presented for a duration of 2 to 8 sec. Eighteen rats were trained to press one lever (the short response) if the signal was shorter than 4 sec, and another lever (the long response) if the signal was longer than 4 sec. When trials were massed (Experiment 1), the percentage long response was affected by the classification of the previous signal, but not by its actual duration. This suggests that the animals remembered the response made on the previous trial, but not the signal duration. If a response was not permitted on the previous trial (Experiment 2), the duration or classification of the previous signal had no effect on performance. This supports the conclusion from the first experiment and suggests that an animal can reset its internal clock in less than 2 sec. In Experiment 3, the difference limen of the psychophysical function increased with the duration of the retention interval, but the point of subjective equality did not change. This suggests that resetting of the internal clock occurs on a non-time dimension.     

Contextual interference effect: elaborative processing or forgetting-reconstruction? A post hoc analysis of transcranial magnetic stimulation-induced effects on motor learning

The elaborative-processing and forgetting-reconstruction hypotheses are the 2 principal explanations for the contextual interference (CI) effect. The present authors' purpose was to identify which of these 2 hypotheses better accounts for the CI effect. They synchronized single transcranial magnetic stimulation (TMS) pulses to each intertrial interval to modulate information processing during Blocked and Random Practice conditions. Participants practiced 3 arm tasks with either a Blocked or Random Practice order. The 3 stimulation conditions (No TMS, TMS, Sham TMS) by 2-practice order (Blocked, Random) between-participant design resulted in 6 experimental groups. Without TMS, motor learning increased under Random Practice. With TMS, this learning benefit diminished. These results support the elaborative-processing hypothesis by showing that perturbing information processing, evoked by Random Practice, deteriorates the learning benefit. Unlike the prediction of the forgetting-reconstruction hypothesis, adding perturbation during Blocked Practice did not significantly enhance motor learning.     

Contextual Interference Effect: Elaborative Processing or Forgetting—Reconstruction? A Post Hoc Analysis of Transcranial Magnetic Stimulation—Induced Effects on Motor Learning

The elaborative-processing and forgetting-reconstruction hypotheses are the 2 principal explanations for the contextual interference (CI) effect. The present authors' purpose was to identify which of these 2 hypotheses better accounts for the CI effect. They synchronized single transcranial magnetic stimulation (TMS) pulses to each intertrial interval to modulate information processing during Blocked and Random Practice conditions. Participants practiced 3 arm tasks with either a Blocked or Random Practice order. The 3 stimulation conditions (No TMS, TMS, Sham TMS) by 2-practice order (Blocked, Random) between-participant design resulted in 6 experimental groups. Without TMS, motor learning increased under Random Practice. With TMS, this learning benefit diminished. These results support the elaborative-processing hypothesis by showing that perturbing information processing, evoked by Random Practice, deteriorates the learning benefit. Unlike the prediction of the forgetting—reconstruction hypothesis, adding perturbation during Blocked Practice did not significantly enhance motor learning.     

Determinants of serial discrimination learning by squirrel monkeys

Squirrel monkeys were presented multiple serial discriminations 1, 2, 4, and 8 problems long. They were then presented problems designed to separate the effects of within-list associative interference from the effects of within-problem intertrial interval as list length was increased. The Ss committed consistently fewer errors after Trial 1 reward than after Trial 1 nonreward and showed strong stimulus perseveration. An increase in within-problem intertrial interval from 30 sec to 4 min had no effect whereas the associative interference resulting from increased problem length caused a small but significant performance decrement. Old and new problems had about equal effects on serial discrimination. The findings indicated that squirrel monkeys are relatively insensitive to within-problem associative interference.     

Context effects on choice.

Four pigeons responded on a concurrent-chains schedule in four experiments that examined whether the effectiveness of a stimulus as a conditioned reinforcer is best described by a global approach, as measured by the average interreinforcement interval, or by a local contextual approach, as measured by the onset of the stimulus preceding the conditioned reinforcer. The interreinforcement interval was manipulated by the inclusion of an intertrial interval, which increased the overall time to reinforcement but did not change the local contingencies on a given trial A global analysis predicted choice for the richer alternative to decrease with the inclusion of an intertrial interval, whereas a local analysis predicted no change in preference. Experiment 1 examined sensitivity to intertrial intervals when each was signaled by the same houselight that operated throughout the session. In Experiment 2, the intertrial interval always was signaled by the stimulus correlated with the richer terminal link. In Experiment 3, the intertrial interval was signaled by the keylights correlated with the initial links and two novel houselights. Experiment 4 provided free food pseudorandomly during the intertrial interval. In all experiments, subjects' preferences were consistent with a local analysis of choice in concurrent chains. These results are discussed in terms of delay-reduction theory, which traditionally has failed to distinguish global and local contexts.     

Rats' lever-press durations as psychophysical judgments of time

Hungry rats received food following lever-press durations exceeding a minimum value, which ranged from 0 to 6.4 sec. When no intertrial intervals separated successive presses, modal press durations remained at very short values as the minimum value required for food was increased. This was particularly true immediately after a food presentation. When an 8-sec intertrial interval followed each lever release, modal press durations were always at or beyond the minimum value required for food, and outcome of the preceding press had no effect on press duration. Possible reasons for the effects of intertrial intervals included punishment of short presses, increased delay of reinforcement of short presses, and reduced density of reinforcement. In addition, functions relating discrete-trials lever-press duration to minimum duration required for food were found to be qualitatively and quantitatively similar to the power functions recently proposed by Catania (1970) for interresponse time and response latency. This similarity was taken as support for a general psychophysical law of temporal judgments.     

An investigation of the perceptual basis of redundancy gain and orthogonal interference for integral dimensions

Redundancy gain and orthogonal interference for height and width were demonstrated in two experiments using a relative coding task with number of intertrial repetitions controlled. Orthogonal interference was shown to be perceptually based rather than simply an intertrial repetitions effect as suggested by Felfoldy (1974). These results from a relative coding task were discussed in terms of the previous multidimensional processing literature. It was concluded that Lockhead’s (1972t model has been applied too generally. An alternative model (a parallel, dimensional analysis stage followed by a stage in which dimensional information is integrated) was suggested.     

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.