Mental load,heart rate and heart rate variability

Summary Several investigators have shown that diminished sinus arrhythmia can be seen as an indication of increased mental load. The present experiment deals with the influence of different levels of mental load, operationalized as the number of binary choices per minute, on the regularity of the heart rate. Also we investigated the influence of four different rest conditions on the regularity of the heart rate.The results show that sinus arrhythmia scores differentiate significantly between several levels of mental load, but heart frequency appeared to be an even better indicator.No significant differences were found between the four rest conditions. Stability over three subsequent measurement sessions was satisfactory, and reliability within the measurement periods was very high.

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Zusammenfassung Mehrere Forscher haben gezeigt, daß abnehmende Sinusarrhythmie betrachtet werden kann als ein Indikator zunehmender mentaler Belastung.In der vorliegenden Untersuchung handelt es sich um den Einfluß verschiedener Niveaus der mentalen Belastung, operationalisiert als die Zahl der binären Wahlen pro Minute, auf die Regelmäßigkeit der Herzfrequenz.Außerdem untersuchten wir den Einfluß vier verschiedener Ruhezustände auf die Regelmäßigkeit der Herzfrequenz.Die Ergebnisse zeigen, daß auf Grund Sinusarrhythmiedaten differenziert werden kann zwischen verschiedenen Niveaus mentaler Belastung, aber die Herzfrequenz erweist sich sogar als ein besserer Indikator.Man stellte keine signifikanten Unterschiede zwischen den vier verschiedenen Ruhezuständen fest.Die Stabilität während drei verschiedener Meßperioden war befriedigend, und die Zuverlässigkeit der Messungen (reliability) innerhalb der Meßperioden war sehr groß.

     

Time, rate, and conditioning

The authors draw together and develop previous timing models for a broad range of conditioning phenomena to reveal their common conceptual foundations: First, conditioning depends on the learning of the temporal intervals between events and the reciprocals of these intervals, the rates of event occurrence. Second, remembered intervals and rates translate into observed behavior through decision processes whose structure is adapted to noise in the decision variables. The noise and the uncertainties consequent on it have both subjective and objective origins. A third feature of these models is their timescale invariance, which the authors argue is a very important property evident in the available experimental data. This conceptual framework is similar to the psychophysical conceptual framework in which contemporary models of sensory processing are rooted. The authors contrast it with the associative conceptual framework.     

Feedback functions, optimization, and the relation of response rate to reinforcer rate

The present experiment arranged a series of inverted U-shaped feedback functions relating reinforcer rate to response rate to test whether responding was consistent with an optimization account or with a one-to-one relation of response rate to reinforcer rate such as linear system theory's rate equation or Herrnstein's hyperbola. Reinforcer rate was arranged according to a quadratic equation with a maximum at a unique response rate. The experiment consisted of two phases, during which 6 Long Evans rats lever pressed for food. In the first phase of the experiment, the rats responded on six fixed-interval-plus-quadratic-feedback schedules, and in the second phase the rats responded on three variable-interval-plus-quadratic-feedback schedules. Responding in both phases was inconsistent with a one-to-one relation of response rate to reinforcer rate. Instead, different response rates were obtained at equivalent reinforcer rates. Responding did vary directly with the vertex of the feedback function in both phases, a finding consistent with optimization of reinforcer rate. The present results suggest that the feedback function relating reinforcer rate to response rate imposed by a reinforcement schedule can be an important determinant of behavior. Furthermore, the present experiment illustrates the benefit of arranging feedback functions to investigate assumptions about the variables that control schedule performance.     

Contact-free measurement of heart rate, respiration rate, and body movements during sleep

We describe a noncontact method for the ambulant measurement of basic sleep physiology parameters in humans, particularly for field studies involving sleep research and sleep disturbances. This method traces the body movements, respiration, and heart action of a person at rest or asleep on a bed, using four high-resolution force sensors installed under the bedposts. The recoil movement of the body at each heartbeat, known as the cardioballistic effect, as well as the lifting and lowering of the thorax, while breathing, causes very small shifts of the center of gravity of the bed and the subject. These shifts are reflected in the altering force distributions across the four sensors. Cardiac and respiratory parameters and the subject’s movement activity can be calculated from the sensor signals. Neither electrodes nor other kinds of transducers are in direct contact with the subject, which is the main advantage of this technique over conventional methods. Laboratory experiments were carried out to estimate validity and practicability. The method has been found to be adequate, especially for automated and unattended sleep-data collection over long periods of time.     

Associations between heart rate,perceived heart rate,and anxiety during acute psychological stress

ABSTRACT

Background: Acute psychological stress elicits increases in heart rate (HR) and anxiety. Theories propose associations between HR, perceived HR, and anxiety during stress. However, anxiety is often measured as a unidimensional construct which limits a comprehensive understanding of these relationships.

Objectives: This research explored whether HR reactivity or perceived HR change was more closely associated with cognitive and somatic anxiety during acute psychological stress.

Design: Two laboratory-based studies were conducted.

Methods: In a single laboratory session, healthy male (N?=?71; study 1) and female (N?=?70; study 2) university students completed three laboratory psychological stress tasks (counterbalanced), each with a preceding baseline. Heart rate, perceived HR change, and cognitive and somatic anxiety intensity and interpretation of anxiety symptoms were assessed immediately following each task. Data were aggregated across tasks.

Results: Actual HR change was unrelated to anxiety intensity, but was associated with more debilitative interpretations of anxiety (study 2). Perceptions of HR change were consistently associated with greater intensity of cognitive (study 1) and somatic (study 1 and 2) anxiety.

Conclusions: Perceived HR rather than actual HR is more closely associated with anxiety intensity during psychological stress. The findings have implications for stress management and the clinical treatment of anxiety symptoms.     

Response rate, latency, and resistance to change

Pigeons were trained on a multiple variable-interval/variable-interval schedule with pacing contingencies that generated high response rates in one component and low response rates in the other. Timeout periods separated the schedule components. During resistance-to-change tests, response-independent food was presented during the timeout periods, and the duration of that food presentation was varied among test sessions. Response rates in the schedule components decreased and latencies to the first response increased as a function of the duration of food presentations during the timeout. Both dependent measures changed about the same amount relative to their own baseline levels. The conclusions are that baseline response rates controlled by pacing contingencies are equally resistant to change, given equal reinforcement densities, and latency is a sensitive measure of resistance to change.     

Anxiety, perception, and control of heart rate

8 women and 8 men took Cattell's IPAT-anxiety questionnaire and later McFarland's test of ability to perceive heart activity. The second test involved subjects' tracking their own heart rates, then they enrolled in an EKG biofeedback session to evaluate ability to increase and decrease heart rate from subjects' resting baselines. At the end of the session each subject completed Blanchard, et al.'s questionnaire to specify the cognitive strategies used for heart-rate control. Heart rate, abdominal respiration rate, respiration amplitude, EEG percent power in theta, alpha, and beta bands were evaluated. Success of heart-rate decrease seemed to depend mainly on activity levels: the subjects who achieved high scores on the activity test decreased heart rate significantly better than did low scorers. The relationship between scores for perception of heart and increases in heart rate was nonsignificant: increased heart-rate seemed to depend on differences in respiration between the rest and periods of increase. The significant, negative correlation between trait anxiety and perceptions of heart activity suggested that anxiety affected subjects' ability to perceive heart rate. The theta EEG power of the right hemisphere was significantly higher in subjects scoring high than for those low in perception of heart activity. During heart-rate increase tasks subjects mainly reported use of 'arousal responses,' similarly during heart-rate decrease tasks they reported use of relaxation responses.     

Response rate, reinforcement frequency, and behavioral contrast

Pigeons responded for food on a multiple schedule in which periods of green-key illumination alternated with periods of red-key illumination. When behavior had stabilized with a variable-interval 2-min schedule of reinforcement operating during both stimuli, low rates of responding (interresponse times greater than 2 sec) were differentially reinforced during the green component. Conditions during the red stimulus were unchanged. Response rates during the green component fell without changing the frequency of reinforcement but there were no unequivocal contrast effects during the red stimulus. The frequency of reinforcement during the green component was then reduced by changing to a variable-interval 8-min schedule without reducing the response rates in that component, which were held at a low level by the spacing requirement. Again, the conditions during the red stimulus were unchanged but response rates during that stimulus increased. These results show that reductions in reinforcement frequency, independently of response rate, can produce interactions in multiple schedules.     

Response rate, reinforcement frequency, and conditioned suppression

In the first of two experiments, periods of noise were terminated with unavoidable shock to 36 rats. The rats' continuously reinforced responding was later completely suppressed during the noise when it was introduced without shock. The rats were then assigned to nine experimental groups. Each group was exposed to different paced variable-interval schedules of reinforcement, which independently controlled response rate and reinforcement frequency. Periods of the noise were periodically superimposed on these schedules, and loss of response suppression was studied. Differences between the groups were assessed statistically. The second experiment used a steady-state design. Six rats were exposed to paced schedules which generated two alternating response rates but gave constant reinforcement frequencies, and six rats to schedules which maintained the same response rates throughout, but in which the reinforcement frequency was alternately high and low. Response suppression was studied during a pre-shock stimulus superimposed on each rat's two behavioral baselines. Both experiments suggest that (1) conditioned suppression is affected by rate of operant responding, high rates being most suppressed, and (2) the frequency of reinforcements obtained also has an effect, most suppression occurring when frequency is low.     

Choice, rate of reinforcement, and the changeover delay

Pigeons distribute their responses on concurrently available variable-interval schedules in the same proportion as reinforcements are distributed on the two schedules only when a changeover delay is used. The present study shows that this equality between proportions of responses and proportions of reinforcements (“matching”) is obtained when the value of the changeover delay is varied. When responses are partitioned into the set of rapid response bursts occurring during the delay interval and the set of responses occurring subsequently, the proportion of neither set of responses matches the proportion of reinforcements. Instead, each set deviates from matching but in opposite directions. Matching on the gross level results from the interaction of two patterns evident in the local response rates: (I) the lengthening of the changeover delay response burst is accompanied by a commensurate decrease in the number of changeovers; (2) the changeover delay response burst is longer than the scheduled delay duration. When delay responses are eliminated by introducing a blackout during the delay interval, response matching is eliminated; the pigeon, however, continues to match the proportion of time spent responding on a key to the proportion of reinforcements obtained on that key.     

Degree of learning,interpolated tests,and rate of forgetting

The purpose of the two experiments reported here was to observe the effects of degree of learning, interpolated tests, and retention interval, primarily on the rate of forgetting of a list of words, and secondarily on hypermnesia for those words. In the first experiment, all the subjects had one study trial on a list of 20 common words, followed by two tests of recall. Half of the subjects had further study and test trials until they had learned the words to a criterion of three correct consecutive recalls. Two days later, half of the subjects under each learning condition returned for four retention tests, and 16 days later, all the subjects returned for four tests. Experiment 2 was similar, except that all the subjects had at least three study trials followed by four recall tests on Day 1, intermediate tests were given 2 or 7 days later, and they all had final tests 14 days later. The results showed that rate of forgetting was attenuated by an additional intermediate set of tests but not by criterion learning. Hypermnesia was generally found over the tests that were given after a retention interval of 2 or more days. The best predictor of the amount of hypermnesia over a set of tests was the difference between overall cumulative recall and net recall on the first test of the set.     

Choice, time allocation, and response rate during stimulus generalization

Six pigeons were trained to discriminate between two noise intensities using a procedure that assessed choice, time allocation, and response rate simultaneously and independently. Responses on the left or right key (R1 or R2) were respectively correct in the presence of two different intensities, S1 and S2. After a correct response, reinforcement became available for pecks on the center key. Reinforcement density for R1¦S1 relative to R2¦S2 was varied across experimental conditions. Generalization tests followed extensive training at each condition. As a function of stimulus intensity, proportions of initial choices of R2, of time spent in R2-initiated components, and of center-key responses emitted in R2-initiated components all yielded sigmoidal gradients of similar slope, which shifted slightly in location when relative reinforcement density changed. Changeovers were maximal where initial choice proportions approximated 0.5. Gradients relating the absolute number of center-key responses to stimulus intensity were also roughly sigmoidal, but were more sensitive to changes in reinforcement density. Gradients of momentary response rate also depended on reinforcement density. During training, large but transitory shifts in choice responding occurred when reinforcement density changed, while differences in momentary response rate developed slowly, suggesting separate control of choice and response rate by the contingencies of reinforcement.     

Wage rate,nonlabor income,and labor supply in rats

Thirsty rats pressed a lever for water under fixed-ratio schedules, with or without free water at the start of the 1-hr session. Total water intake fell steadily as the fixed-ratio requirement increased; when the fixed-ratio requirements covered a relatively broad range, total lever presses rose and then fell as the requirement increased. Free water decreased total lever presses but increased total intake, especially at the higher fixed-ratio requirements; its effect on total intake proved relatively hard to detect, but grew more apparent as the amount of free water increased. The results conformed more closely to a recent revision of the conservation model than to the original model. By viewing milliliters per press as a wage rate, and free water as nonlabor income, results are brought to bear on predictions derived from economic labor supply theory. In economic terms, rising wage rates were accompanied by a rise followed by a fall in total labor supply, but a steady rise in total income, in conformity with the backward bending labor supply curve. Nonlabor income cut the supply of labor but raised total income, especially at the lower wage rates.