The effects of number of responses on the postreinforcement pause in fixed-interval schedules

The present study manipulated the number of responses in a modified fixed-interval schedule by imposing a blackout after each unreinforced response during the interval. The blackout duration was varied, and the duration of the fixed interval was held constant. The subjects were initially exposed to a fixed-interval 300-sec schedule. Blackout durations of 0, 10, and 50 sec were used. Following this, a fixed-interval 30-sec schedule was used with blackout durations of 0, 1, and 5 sec. Under the fixed-interval 300-sec schedule, the number of interreinforcement responses varied over a wider range than occurred under the fixed-interval 30-sec schedule. The duration of the postreinforcement pause decreased as blackout durations were increased and number of responses decreased on the fixed-interval 300-sec schedule, but pause length did not vary with changes in blackout duration and number of responses for the fixed-interval 30-sec schedule. The differences in the effects of blackout duration and response manipulation on the two fixed-interval schedules were attributed to relatively greater changes in the number of interreinforcement responses for the fixed-interval 300-sec schedule.     

The effects of stem length and directions on sentence completion test responses

In an investigation of the effects of stem structure and direction set on sentence completion responses, 160 undergraduate males were randomly assigned to one of four conditions: Rotter ISB with "feelings" instructions, Rotter ISB with "speed" instructions, Sacks SCT with "feelings" instructions, Sacks SCT with "speed" instructions. Eight clinical judges derived hypotheses from the completed protocols; two judges evaluated each protocol. Interjudge reliability was measured by Pearson product-moment correlations and percents of agreement. There was a significant effect for amount of stem structure; the structured Sacks SCT stems yielded more clinical hypotheses. Structured stems also elicited significantly more feeling words. No significant effect was found for instructional set, nor was there a significant relationship between stem structure or instruction set and the numbers of words in completions.     

Drug effects on fixed-interval responding with pause requirements for food presentation.

In pigeons performing under a multiple schedule of food presentation, low key-pecking rates (0.18 to 0.29 responses per second) were maintained during 3-min fixed-interval components by requiring a 4-, 5-, or 6-sec pause preceding the food-delivery response (tandem DRL), while higher rates (0.70 to 1.37 responses per second) were maintained in alternative fixed-interval components by requiring a pause of no more than 40 msec preceding the food-delivery response (tandem DRH). Thus, reinforcement density was equal but overall response rates markedly different in the two schedule components. Pentobarbital (3, 10 mg/kg) had effects on overall rates of responding consistent with a rate-dependency interpretation (low rates were increased while higher rates were decreased), but d-amphetamine (0.03 to 3 mg/kg) either failed to increase low overall rates in the tandem DRL components or increased them only slightly. Effects of both drugs on local responding within the fixed-intervals were always related in an orderly way to control response rate, but the extent of rate increases produced by d-amphetamine was modifed in some birds by pause requirements such that the drug increased comparable rates less when these occurred in the tandem DRL component than when they occurred in the tandem DRH components. Control rate is an important determinant of drug effects, independent DRH components. Control rate is an important determinant of drug effects, independent of reinforcement density maintaining rates, and independent of environmental influences, such as response-spacing requirements for food presentation, that can modify the extent of some drug-produced rate changes.     

The effects of acute exercise on temporal generalization

Sixteen healthy college students performed a multiple-trial referenced temporal generalization task and an episodic temporal generalization task before and during moderate-intensity aerobic exercise. The same tasks were performed in a resting control condition. Working memory tasks were also administered before, during, and after exercise to determine whether exercise affected working memory processes. Temporal generalization gradients demonstrated leftward shifts during exercise when compared to rest, indicating that the subject perceived intervals to elapse more slowly. This finding is consistent with an increased pacemaker speed. Subjective lengthening of stimuli as the task progressed did not occur during exercise or rest. No significant differences were observed on the episodic timing task, nor were any differences found on the working memory tasks. These findings provide support for the notion that exercise influences the internal clock in a manner similar to other arousal-inducing manipulations.     

The effects of temporal waveform upon temporal darkness enhancement

Temporal darkness enhancement refers to the finding that decremental flashes of 50–140 msec appear darker than longer flash decrements. The present experiment determined the effects of temporal waveform upon darkness enhancement by obtaining darkness judgments for flashes that had abrupt onset/abrupt offset, abrupt onset/gradual offset, gradual onset/abrupt offset, and gradual onset/gradual offset. Temporal darkness enhancement was found only for flashes that had abrupt onsets regardless of offset waveform. These results are discussed in terms of the role of transients in the coding of perceived darkness.     

The effects of acute exercise on temporal generalization

Sixteen healthy college students performed a multiple-trial referenced temporal generalization task and an episodic temporal generalization task before and during moderate-intensity aerobic exercise. The same tasks were performed in a resting control condition. Working memory tasks were also administered before, during, and after exercise to determine whether exercise affected working memory processes. Temporal generalization gradients demonstrated leftward shifts during exercise when compared to rest, indicating that the subject perceived intervals to elapse more slowly. This finding is consistent with an increased pacemaker speed. Subjective lengthening of stimuli as the task progressed did not occur during exercise or rest. No significant differences were observed on the episodic timing task, nor were any differences found on the working memory tasks. These findings provide support for the notion that exercise influences the internal clock in a manner similar to other arousal-inducing manipulations.     

Separating the effects of interreinforcement time and number of interreinforcement responses

The relative importance of interreinforcement time and interreinforcement responses was evaluated by varying each independently. To do this, a blackout was presented after each nonreinforced response under both fixed-ratio and fixed-interval schedules of reinforcement. Manipulating the blackout duration under the fixed-ratio schedule caused interreinforcement time to vary without affecting the number of interreinforcement responses. Pigeons' post-reinforcement and post-blackout response latencies were found to increase linearly with interreinforcement time. Under the fixed-interval schedule, the same blackout manipulations changed the number of interreinforcement responses without affecting interreinforcement time. Post-reinforcement and post-blackout response latencies under this condition were approximately constant. These results suggest that responding is controlled by interreinforcement time and is not influenced by the number of responses emitted between reinforcements.     

The effects of spatial,temporal, and control variables on the free-recall serial position curve of retardates and equal-MA normals

Memory & Cognition - In Experiment I seven pictures were sequentially illuminated at a 3-see rate through seven translucent windows. A different window provided the starting point for each of...     

The effects of spatial frequency and temporal waveform on three measures of temporal processing

The effects of spatial frequency and temporal transition of sine-wave grating onset and offset were assessed using measures of reaction time, visual persistence, and temporal order judgements. The stimuli were lateralized fields, separated by 1 degree of visual angle. Slow temporal transition resulted in significantly poorer performance than did abrupt onset and offset, but spatial frequency had a minimal effect. Thus, the latency, temporal resolution, and temporal ordering of events are mediated by a mechanism that is sensitive to abrupt temporal transients. The stimulus conditions employed did not result in a shift in the point of subjective simultaneity.     

The effects of ordinal load on incidental temporal learning

How can we grasp the temporal structure of events? A few studies have indicated that representations of temporal structure are acquired when there is an intention to learn, but not when learning is incidental. Response-to-stimulus intervals, uncorrelated temporal structures, unpredictable ordinal information, and lack of metrical organization have been pointed out as key obstacles to incidental temporal learning, but the literature includes piecemeal demonstrations of learning under all these circumstances. We suggest that the unacknowledged effects of ordinal load may help reconcile these conflicting findings, ordinal load referring to the cost of identifying the sequence of events (e.g., tones, locations) where a temporal pattern is embedded. In a first experiment, we manipulated ordinal load into simple and complex levels. Participants learned ordinal-simple sequences, despite their uncorrelated temporal structure and lack of metrical organization. They did not learn ordinal-complex sequences, even though there were no response-to-stimulus intervals nor unpredictable ordinal information. In a second experiment, we probed learning of ordinal-complex sequences with strong metrical organization, and again there was no learning. We conclude that ordinal load is a key obstacle to incidental temporal learning. Further analyses showed that the effect of ordinal load is to mask the expression of temporal knowledge, rather than to prevent learning.     

The situational effects on haptic perception of rod length

Three experiments were conducted to investigate situational effects (manipulation, range, and prior experience) on the haptic perception of rod length. Each rod was held between its two ends with one hand. In Experiment 1, 32 participants judged length of rods using different manipulations. Perceived lengths were found to be dependent on manner of manipulation and not necessarily equal to actual lengths. Different parameters were detected in different manipulations. In Experiment 2, 8 participants judged rod lengths by wielding rods of two ranges: long and short. Perceived length was found to be affected by the range of rods evaluated successively in a single set. In Experiment 3, 9 participants judged rod lengths after an experience of handling dense or light rods. Perceived length was found to be affected by prior experience. Results are discussed in terms of how rod lengths can be perceived accurately by haptic modality without involving direct perception.     

The force/force-variability relationship under controlled temporal conditions

Previously, an inverted U relationship between force and force variability was demonstrated in both static and dynamic responses. Recent research suggests that the inverted U function may be due to a lack of control of the temporal aspects of the response. To investigate this hypothesis, we examined the relationship between force and force variability in rapid movements under controlled temporal conditions. Subjects (N = 4) made rapid reversal responses with a horizontal lever (using elbow flexion and extension) such that the time to reversal (160 ms) and the distance to reversal (45 degrees ) were held constant in each of six load conditions (either 0,.260,.780, 1.040, or 1.560 kg added to the lever). When time to reversal and time to peak acceleration were held constant, a curvilinear relationship between force and force variability resulted, suggesting that the inverted U function is related to control of the temporal aspects of the response.     

The effects of marker-related temporal cues on auditory gap-duration discrimination

In three experiments, we examined the ability of listeners to discriminate the duration of temporal gaps (silent intervals) and the influence of other temporal stimulus properties on their performance. In the first experiment, gap-duration discrimination thresholds were measured either in continuous noise or with noise markers with durations of 3 and 300 ms. Thresholds measured with 300-ms markers differed from those measured in continuous noise or with 3-ms markers. In the second experiment, stimuli consisting of a gap between two discrete markers were generated such that the gap duration, the onset-to-onset duration between markers, and the duration of the first marker were pseudorandomized across trials. Listeners’ responses generally were consistent with the cue that was identified as the target cue from among the three cues in each block of trials, but the data suggested that the onset-to-onset cue was particularly salient in all conditions. Using a modified method-of-adjustment procedure in the third experiment, subjects were instructed to discriminate between the durations of gaps in discrete markers of different durations in two intervals, where the gap duration in one interval was adapted to measure the point of subjective equality. Without feedback, listeners tended to equate the onset-to-onset times of the markers rather than the gap durations. Overall, the results indicated that listeners’ judgments of silent gaps between two discrete markers are strongly influenced by the onset-to-onset time, or rhythm, of the markers.