DOES CONTINGENT REINFORCEMENT STRENGTHEN OPERANT BEHAVIOR?

In Experiment 1, pigeons were trained to peck keys with equal food-reinforcement schedules in components that ended with either noncontingent or contingent transitions to a third component with a five-fold richer schedule. Response rates were higher in the initial component with contingent transitions, but resistance to prefeeding or extinction was not consistently greater. Experiment 2 also included noncontingent or contingent transitions to a signaled period of nonreinforcement. There was no effect of the contingency on transitions to nonreinforcement, but the difference in response rates maintained by contingent versus noncontingent transitions to the richer schedule was replicated. In addition, response rates were higher in components that preceded nonreinforcement than in components that preceded the richer schedule. However, resistance to extinction was greater for noncontingent transitions to the richer schedule than to nonreinforcement, implicating stimulus–reinforcer relations in the determination of resistance to change. Resistance to change was also somewhat greater for noncontingent than for contingent transitions to the richer schedule. The latter result, together with the results of Experiment 1 and related research, suggests that response-contingent reinforcement does not increase resistance to change.     

Cardiac-somatic integration: An index of visual attention

Eighteen 15-week-old, normal full-term infants were presented with photographic slides of a human facial expression. The infant's heart rate, body movement, and visual attention were recorded simultaneously. The results showed that heart rate and body movement were significantly correlated during visual attention but not during inattention. Both heart rate and body movement decelerated significantly when the infants visually attended to the target stimulus. The results are discussed with reference to cardiac-somatic integration in early infancy and its implication as a possible index of attention.     

Temporal discrimination and a free-operant psychophysical procedure.

Pigeons were presented a series of keylight time periods (separated by blackouts) during which two response keys were lit, one by blue light and the other either by orange or green. Blue-key responses changed the color on the other key. Orange-key responses sometimes produced food during the first half of a time period; green-key responses sometimes produced food during the second half. In three experiments, the probability of a green-key response increased as a function of elapsed time. Experiment 1 compared performance when the duration of the keylight periods was varied across a wide range. Discrimination of performance was similar across the range of durations. Experiment 2 varied both relative reinforcement rate and the local reinforcement rate for orange-key and green-key responses. These manipulations produced changes in response bias but not discrimination sensitivity. Experiment 3 varied the local temporal placement of reinforcers within time periods and demonstrated that choice behavior was affected by differential reinforcement at different points during the time periods. The results were consistent with previous research on duration discrimination that used psychophysical trials procedures.     

Statistical inference for false positive and false negative error rates in mastery testing

This paper describes an asymptotic inferential procedure for the estimates of the false positive and false negative error rates. Formulas and tables are described for the computations of the standard errors. A simulation study indicates that the asymptotic standard errors may be used even with samples of 25 cases as long as the Kuder-Richardson Formula 21 reliability is reasonably large. Otherwise, a large sample would be required.This work was performed pursuant to Grant No NIE-G-78-0087 with the National Institute of Education, Department of Health, Education and Welfare, Huynh Huynh, Principal Investigator. Points of view or opinions stated do not necessarily reflect NIE position or policy and no official endorsement should be inferred. The editorial assistance of Joseph C. Saunders is gratefully acknowledged.     

RESPONSE INTERRUPTION AND DRL FOR THE REDUCTION OF RAPID EATING

We assessed the efficacy of several procedures for reducing the rate of eating responses during mealtime by three institutionalized mentally retarded clients. A time-based (15 s) response interruption procedure was implemented which resulted in little change in eating responses for 2 of 3 subjects. A spaced-responding DRL 15-s procedure resulted in decreases in eating responses to target levels only after a prompting procedure was added. Procedures were evaluated using a multiple baseline across subjects design with assessment of generalization to nontreated meals. A change in eating behavior during breakfast occurred only after direct training in the breakfast setting. Maintenance data were collected at 1- and 5-month follow-up periods.     

Reanalysis of the equation for simple action

De Villiers and Herrnstein (1976) have shown that the equation for simple action, derived from the matching law, predicts change in behavioral output for some 40 experiments in which the value of a single source of reinforcement has been varied. Using only the positive-reinforcement studies they cite that used five or more different reinforcement values, we found the high percentage of variance they report accommodated by this equation (94%) is predicated on instances of averaging rates of behavioral output before making a least-squares fit of the equation. In our reanalysis, which minimizes rate averaging, only 78% of the data variance is accommodated. This diminished data-variance accommodation can be improved by adding parameters that permit the equation's scaling constant to change as a function of reinforcement. Although these parameters permit acceptable levels of accommodation of data variance, they correspond to no obvious psychological processes. These findings support the view that the equation for simple action is an inadequate model for behavioral output.     

Greater reinforcement rate during training increases spontaneous recovery

Spontaneous recovery occurs when a previously reinforced and recently extinguished response reemerges over the course of time, often at the beginning of a new session of extinction. Spontaneous recovery could underlie instances of treatment relapse that threaten otherwise effective behavioral interventions for problem behavior. In two experiments, we arranged multiple schedules with pigeons and a human child to assess the effects of different training reinforcer rates on spontaneous recovery. In both experiments, responding was both more resistant to extinction and more likely to relapse following training with greater reinforcement rates upon returning to extinction after time off from extinction testing. A quantitative model based on behavioral momentum theory accounted well for the data, which suggests reexposure to the extinction context following time off during extinction resulted in (1) the failure of extinction learning to generalize, and (2) greater generalization of original learning during training. The present model attempts to quantify theories attributing spontaneous recovery to changes in temporal context.     

Influence of Accelerometer Placement and/or Heart Rate on Energy Expenditure Prediction during Uphill Exercise

Studies using a triaxial accelerometer and heart rate (HR) simultaneously for estimating energy expenditure (EE) during uphill exercise are rare. Exploring the optimal location for placing the accelerometer for predicting EE during uphill exercise is essential. Sixteen healthy male participants (M ± SEM; age 25.00 ± 0.61 years; body weight 74.13 ± 2.51 kg; body height 1.74 ± 0.01 m; body mass index 24.30 ± 0.63 kg/m²) exercised on a treadmill under 12 conditions (4 speeds and 3 gradients) on 3 days. Triaxial accelerometers, an HR recorder, and a metabolic measurement system were simultaneously used. Accelerometer outputs from various anatomical locations (upper arm, chest, lower back, waist, thigh, and instep) showed significant positive correlations with EE (0.819, 0.846, 0.816, 0.820, 0.672, and 0.669, respectively; p < .05). The linear regression equation for changes in HR showed the highest coefficient of determination (r²) of .837 with 87.9% reliability. When the HR signal was included, the r² value (> .842) and reliability (87.9%) between the accelerometer outputs and EE improved. Accelerometer outputs from the waist position alone provide highly accurate EE values. Using both accelerometer outputs and HR for EE estimation during uphill exercise is feasible and improves the accuracy of EE prediction.     

Mentalizing eye contact with a face on a video: Gaze direction does not influence autonomic arousal

Recent research has revealed enhanced autonomic and subjective responses to eye contact only when perceiving another live person. However, these enhanced responses to eye contact are abolished if the viewer believes that the other person is not able to look back at the viewer. We purported to investigate whether this “genuine” eye contact effect can be reproduced with pre‐recorded videos of stimulus persons. Autonomic responses, gaze behavior, and subjective self‐assessments were measured while participants viewed pre‐recorded video persons with direct or averted gaze, imagined that the video person was real, and mentalized that the person could see them or not. Pre‐recorded videos did not evoke similar physiological or subjective eye contact effect as previously observed with live persons, not even when the participants were mentalizing being seen by the person. Gaze tracking results showed, however, increased attention allocation to faces with direct gaze compared to averted gaze directions. The results suggest that elicitation of the physiological arousal in response to genuine eye contact seems to require spontaneous experience of seeing and of being seen by another individual.     

Automatic semantic encoding in verbal short-term memory: Evidence from the concreteness effect

The concreteness effect in verbal short-term memory (STM) tasks is assumed to be a consequence of semantic encoding in STM, with immediate recall of concrete words benefiting from richer semantic representations. We used the concreteness effect to test the hypothesis that semantic encoding in standard verbal STM tasks is a consequence of controlled, attention-demanding mechanisms of strategic semantic retrieval and encoding. Experiment 1 analysed the effect of presentation rate, with slow presentations being assumed to benefit strategic, time-dependent semantic encoding. Experiments 2 and 3 provided a more direct test of the strategic hypothesis by introducing three different concurrent attention-demanding tasks. Although Experiment 1 showed a larger concreteness effect with slow presentations, the following two experiments yielded strong evidence against the strategic hypothesis. Limiting available attention resources by concurrent tasks reduced global memory performance, but the concreteness effect was equivalent to that found in control conditions. We conclude that semantic effects in STM result from automatic semantic encoding and provide tentative explanations for the interaction between the concreteness effect and the presentation rate.