Effect of interval between auditory and preceding visual stimuli on auditory sensitivity

Auditory thresholds were determined by a modified method of limits, in introverts, ambiverts and extraverts, under three intensities of light. Five determinations were made: one before, one during and three (30 sec., c. 8 and 16 min.) after the light stimulation. An analysis of variance of the data showed significant results for the interval conditions, the personality type and the interaction of these parameters, under the weak light. Interval effects were also significant under medium and strong light. A weak light increased, and a strong light decreased, auditory sensitivity when threshold determinations began 30 sec., but not more than about 8 min., after the light stimulation, in introverts.     

Reliability of auditory responses under increasing intensity of visual stimulation in relation to personality

Auditory thresholds were determined in each subject on two different occasions, by a modified method of limits under 10 intensities of light. Coefficients of reliability and analyses of variance of the data showed significant reliability of responses to tones in introverts (I) and extraverts (E), under increasing intensities of light. The auditory responses were most reliable in I and least in ambiverts (A). The same visual stimuli produced the same effects on auditory sensitivity, in the same subjects, on different days. These effects included facilitation and inhibition of sensitivity in I, facilitation in E and A, and interaction of intensity conditions and personality type.     

SENSORY AND PREPARATORY FACTORS IN RESPONSE LATENCY

T hrane , V. C. Sensory and preparatory factors in response latency. IV. General and differential warning of full-scale auditory intensities. Scand. J Psychol ., 1961, 2, 211–224.—Twenty-one loudness variants ranging from hardly audible to no db re standard threshold were randomly presented after either (1) a constant or (2) a varied warning signal denoting one range below and two above an assumed transition point for the bi-functional relationship between response latency and stimulus intensity. Under (1) greater improvement with practice at one end of the scale was acccompanied by smaller gains at the other end. Under (2) practice had favorable but preknowledge unfavorable effects at the weakest intensities. Differential warning facilitated speed of response only for medium and strong stimuli and most at the high end of the scale.     

Sensation seeking, augmenting-reducing, and absolute auditory threshold: a strength-of-the-nervous-system perspective

The following measures were obtained from 42 student volunteers: the General and the Disinhibition subscales of the Sensation Seeking Scale (Form IV), the Reducer-Augmenter Scale, and the Absolute Auditory Threshold. General sensation seeking correlated significantly with the Reducer-Augmenter Scale, r(40) = .59, p less than .001, and the Absolute Auditory Threshold, r(40) = .45, p less than .005. Both results proved general across sex. These findings, that high-sensation seekers tend to be reducers and to lack sensitivity to weak stimulation, were interpreted as supporting strength-of-the-nervous-system theory more than the formulation of Zuckerman and his associates.     

When increased confidence yields increased thought: A confidence-matching hypothesis

Traditional theories of confidence and information processing suggest that people engage in greater processing activity when they feel doubtful as opposed to confident. Recent research, however, has hinted at the possibility that this effect might be malleable. The current research tests a confidence-matching hypothesis to determine when increased confidence yields increased processing and when increased confidence yields decreased processing. Based on recent advances in research on matching effects, it is proposed that the classic negative effect of confidence on information processing will reverse when messages are framed in terms of confidence. This hypothesis is tested by presenting participants with a persuasive message containing strong or weak arguments under confidence or doubt conditions. As predicted, when the message is framed in confidence terms, participants engage in greater message processing when they feel confident rather than doubtful, as indicated by greater argument quality effects on attitudes and thought favorability.     

Cortical evoked potentials as indicators of auditory-visual cross-modal association in young adults

Auditory evoked potentials (AEPs) were studied from scalp locations Cz and Oz on 37 adults aged 20–22 years during sensori-sensorial association of a weak sound (S) and a strong flash of light (L). After sound alone repetition (habituation), S-L association modified AEP: first, it caused a generalized orienting response expressed as increasing of Cz and Oz amplitude AEPs. Then, this pattern gave way to an activation limited to the Oz lead: the increase of amplitude was then concomitant with shortened latencies when compared to sound-alone-habituated responses. Inter-individual differences were observed since these occipital modifications were recorded only on 26 subjects. The other 11 subjects did not exhibit any occipital modifications following S-L association. For them, the main modification was a strong decrease of Cz AEP induced by S-L association. These two groups also differed in their capacity to ignore irrelevent stimuli which is higher in the first group (AEP amplitude habituation with sound-alone repetition) than in the second one (no AEP habituation).     

Studies of nervous system sensitivity in children with learning and attention disorders

Clinically referred children, diagnosed as having learning or attention disorders, with or without hyperactivity, were found to vary widely on a measure of nervous system sensitivity recommended by the Pavlovian investigator Vasilev. That is, the children were contrasted on their mean press and release reaction times (RTs) to four tones, ranging from soft (55 db) to very loud (100 db), with the expectation that some would be able to maintain a parallel separation of press and release RT gradients across all intensity levels (strength), whereas others would show convergence or overlap of the gradients at higher intensities (weakness). Contrary to expectation, girls did not have weaker or more sensitive nervous systems than boys, although the girls rated themselves as less tolerant of intense stimuli. Significantly more of the children diagnosed as hyperactive had weaker nervous systems. The boys also participated in a blind crossover study contrasting placebo and methylphenidate effects; the prescribing physician, who was not informed of the child’s nervous system classification, adjusted the dosage levels so that subjects with weaker nervous systems were titrated at higher dosage levels than those with stronger nervous systems. Gray (1964) suggested an explanation of this paradox, i.e., that the weak nervous system requires a more intense stimulus than the strong to reach the threshold of concentration (or focused attention), whereas for other thresholds the strong requires a more intense stimulus than the weak. Gray’s theory was further supported by the finding that children typed as weak (unmedicated) did not show as great facilitation in RT with reward (moderate stimulus) as did those typed as strong.     

Effects of nonconscious perception on motor response

The present study reviews the literature on the empirical evidence for the dissociation between perception and action. We first review several key studies on brain-damaged patients, such as those suffering from blindsight and visual/tactile agnosia, and on experimental findings examining pointing movements in normal people in response to a nonconsciously perceived stimulus. We then describe three experiments we conducted using simple reaction time (RT) tasks with backward masking, in which the first (weak) and second (strong) electric stimuli were consecutively presented with a 40-ms interstimulus interval (ISI). First, we compared simple RTs for three stimulus conditions: weak alone, strong alone, and double, i.e., weak plus strong (Experiment 1); then, we manipulated the intensity of the first stimulus from the threshold (T) to 1.2T and 2T, with the second stimulus at 4T (Experiment 2); finally, we tested three different ISIs (20, 40, and 60 ms) with the stimulus intensities at 1.2T and 4T for the first and second stimuli (Experiment 3). These experiments showed that simple RTs were shorter for the double condition than for the strong-alone condition, indicating that motor processes under the double condition may be triggered by sensory inputs arising from the first stimulus. Our results also showed that the first stimulus was perceived without conscious awareness. These findings suggested that motor processes may be dissociated from conscious perceptual processes and that these two processes may not take place in a series but, rather, in parallel. We discussed the likely mechanisms underlying nonconscious perception and motor response to a nonconsciously perceived stimulus.     

Absolute sensitivity to white noise under auxiliary visual stimulation1

Absolute sensitivity to white noise was measured with the O in the dark, in constant illumination, and in the dark but with sound-synchronized flashes of light at three different intensities. A confidence rating procedure was used, and the results were analyzed in terms of the theory of signal detectability. There appeared to be no consistent effect of auxiliary visual stimulation on absolute auditory sensitivity for the four Os examined.     

Loudness and reaction time: II Identification of detection components at different intensities and frequencies

Equal-loudness contours were first obtained for five stimulus frequencies at four stimulus intensities. These 20 stimuli were then presented as reaction-time signals in a Donders C paradigm. The Z-transform method of convolution, as applied in linear systems identification, was used to deconvolve an empirically generated response (or “residual”) distribution (T_R) from each of the 20 reaction-time (RT) distributions obtained at different intensities and frequencies. The resulting sensory-detection (t_d) models formed exponential densities at strong intensities (60 and 80 phons), but their shapes were either gamma or normal at relatively weak intensities (20 and 40 phons). Our analyses support the idea that the simple reactiontime process (RT) is a convolution (or sum) of two component stages: stimulus detection (t_d), followed by response evocation (t_r). Based on the shapes of t_d, a neural-impulse theory is offered to account for the detection of simple auditory RT signals.     

Weight as an Embodiment of Importance

ABSTRACT— Four studies show that the abstract concept of importance is grounded in bodily experiences of weight. Participants provided judgments of importance while they held either a heavy or a light clipboard. Holding a heavy clipboard increased judgments of monetary value (Study 1) and made participants consider fair decision-making procedures to be more important (Study 2). It also caused more elaborate thinking, as indicated by higher consistency between related judgments (Study 3) and by greater polarization of agreement ratings for strong versus weak arguments (Study 4). In line with an embodied perspective on cognition, these findings suggest that, much as weight makes people invest more physical effort in dealing with concrete objects, it also makes people invest more cognitive effort in dealing with abstract issues.     

Effects of stimulus control and deprivation upon discriminative responding

Discriminative responding in pigeons was studied under multiple variable-interval extinction schedules in which extinction was correlated with either a tone or a white keylight. The two procedures resulted in weak and strong stimulus control, respectively. In the first experiment, there was no interaction between schedule components when stimulus control was strong and reinforcement was omitted under the previously reinforced component. However, there was marked induction between components when stimulus control was weak and responding was extinguished under the previously reinforced component. In the second experiment, hours of food deprivation was varied under two levels of stimulus control. Deprivation mainly influenced response rates under the extinction stimulus, with greater absolute rate increases occurring the lower the existing level of stimulus control. Increases in responding during the extinction stimulus were four times as great from 24 to 72 hours of deprivation as from 24 to 48 hours under conditions of both high and low stimulus control.     

Effects of varying stimulus disparity and the reinforcer ratio in concurrent-schedule and signal-detection procedures.

The present study measured the effects of stimulus and reinforcer variations on pigeons' behavior in two different choice procedures. Two intensities of white light were presented as the stimuli on the main key in a switching-key concurrent schedule and as the sample stimuli in a signal-detection procedure. Under both procedures, the scheduled rate of reinforcement was varied across conditions to produce various ratios of obtained reinforcement. These ratios were obtained for seven pairs of light intensities. In the concurrent schedules, the effects of reinforcer-ratio variations were positively correlated with the physical disparity between the two light intensities. In the signal-detection procedure, changes in the reinforcer ratio produced greater effects on performance when stimulus disparity was very low or very high compared to those found at intermediate levels of stimulus disparity. This discrepancy creates a dilemma for existing behavioral models of signal-detection performance.     

Scotopic sensitivity in coyotes (Canis latrans).

The absolute scotopic limen for light intensity was measured for three 10-mo-old female coyotes. The methodology was similar to that used by Blough in determining psychophysical thresholds in pigeons. Three coyotes were operantly conditioned to depress one of two foot treadles, left or right, depending on the condition of the stimulus light. Scotopic adaptation curves for each coyote were generated. Nonlinear regression curves were then fitted to the raw data. The mean scotopic thresholds did not differ significantly. However, time to the curves' asymptotes did differ significantly for one of the coyotes. The adaptation curves showed a distinct rod-cone "break," and retinal histology confirmed that the coyote has a duplex retina with a preponderance of rods. In addition, electroretinographic analysis showed the relative contributions of rods and cones at various light intensities and indicated a rod-cone break at approximately 15 min. Scotopic spectral sensitivity curves were also generated. The coyotes' scotopic visual threshold is exceeded by the natural illumination available under many nocturnal conditions. The results are discussed in relation to the ecology of the species.     

Moderating influences of hypnotic susceptibility on signal-detection task performance

This study investigated the differential influence of hypnotic susceptibility level on signal detection task (SDT) performance in waking and hypnotic conditions. As assessed by the Harvard Group Scale of Hypnotic Susceptibility, Form A (HGSHS: A) and the Stanford Hypnotic Susceptibility Scale, Form C (SHSS: C), 20 high (9–12), 20 medium (4–8), and 20 low (0–3) hypnotizables participated. In counterbalanced conditions of waking and hypnosis, Ss (Subjects) were given 36 signal detection trials, consisting of 12 strong signals, 12 weak signals, and 12 “no” signals. No differences were observed in the waking condition between low, medium, and high hypnotizables on strong and weak signal trials. In hypnosis, high hypnotizables exhibited significantly superior performance on the strong signal trials in comparison with low hypotizables, and performed significantly better on the weak signal trials than did the low and medium hypnotizables. Low and medium hypnotizables performed similarly in waking and hypnotic conditions, while high hypnotizables showed significant enhancements in performance for strong and weak signal trials during hypnosis. This research was supported, in part, by a grant from Fort Hays State University.     

Moderating influences of hypnotic susceptibility on signal-detection task performance

This study investigated the differential influence of hypnotic susceptibility level on signal detection task (SDT) performance in waking and hypnotic conditions. As assessed by the Harvard Group Scale of Hypnotic Susceptibility, Form A (HGSHS: A) and the Stanford Hypnotic Susceptibility Scale, Form C (SHSS: C), 20 high (9–12), 20 medium (4–8), and 20 low (0–3) hypnotizables participated. In counterbalanced conditions of waking and hypnosis, Ss (Subjects) were given 36 signal detection trials, consisting of 12 strong signals, 12 weak signals, and 12 “no” signals. No differences were observed in the waking condition between low, medium, and high hypnotizables on strong and weak signal trials. In hypnosis, high hypnotizables exhibited significantly superior performance on the strong signal trials in comparison with low hypotizables, and performed significantly better on the weak signal trials than did the low and medium hypnotizables. Low and medium hypnotizables performed similarly in waking and hypnotic conditions, while high hypnotizables showed significant enhancements in performance for strong and weak signal trials during hypnosis. This research was supported, in part, by a grant from Fort Hays State University.     

Morningness–eveningness orientation and attitude change: Evidence for greater systematic processing and attitude change at optimal time-of-day

This study examines the relationship between morningness–eveningness orientation and time-of day on attitude change, and tests the hypothesis that people will be more persuaded when tested at their optimal time-of-day (i.e., morning for M-types and evening for E-types) than non-optimal time-of-day (i.e., evening for M-Types and morning for E-types). Two hundred and twenty participants read a message that contained either strong vs. weak quality counter-attitudinal arguments (anti-voluntary euthanasia) in the morning (9.00 a.m.) or in the evening (7.00 p.m.). When tested at their respective optimal time-of-day (for both M- and E-types) there was a reliable difference in attitude change between the strong vs. weak messages (indicating message processing had occurred) while there was no difference between strong vs. weak messages when tested at their non-optimal time-of-day. In addition, the amount of message-congruent thinking mediated the attitude change. The results show that M- and E-types pay greater attention to and elaborate on a persuasive message at their optimal time-of-day, and this leads to increased attitude change, compared to those tested at their non-optimal time-of-day.     

Social anxiety and interpretation biases for facial displays of emotion: emotion detection and ratings of social cost

The current study assessed the processing of facial displays of emotion (Happy, Disgust, and Neutral) of varying emotional intensities in participants with high vs. low social anxiety. Use of facial expressions of varying intensities allowed for strong external validity and a fine-grained analysis of interpretation biases. Sensitivity to perceiving negative evaluation in faces (i.e., emotion detection) was assessed at both long (unlimited) and brief (60 ms) stimulus durations. In addition, ratings of perceived social cost were made indicating what participants judged it would be like to have a social interaction with a person exhibiting the stimulus emotion. Results suggest that high social anxiety participants did not demonstrate biases in their sensitivity to perceiving negative evaluation (i.e. disgust) in facial expressions. However, high social anxiety participants did estimate the perceived cost of interacting with someone showing disgust to be significantly greater than low social anxiety participants, regardless of the intensity of the disgust expression. These results are consistent with a specific type of interpretation bias in which participants with social anxiety have elevated ratings of the social cost of interacting with individuals displaying negative evaluation.     

Malleability of conditioned associations: path dependence

Using conditioned suppression of barpressing to investigate the stability of a conditioned stimulus-unconditioned stimulus (CS-US) association, we gave water-deprived rats either a few pairings of the CS with a strong footshock US or many pairings with a weak footshock US so that barpress suppression in response to the CS was equated. Experiment 1 established training parameters that yielded this equivalence. Specifically, rapid acquisition to a preasymptotic level of responding with strong shock produced suppression comparable to the asymptotic level reached more slowly with weak shock. Experiment 2 showed that although equivalent performance was obtained from extensive conditioning with a weak shock or limited conditioning with strong shock, only extensive conditioning with weak shock resulted in retarded acquisition of an association between that same CS and a footshock level perceived as midway between the two initial training shock intensities as implied by asymptotic performance in Experiment 1. Experiment 3 demonstrated that the observed retardation in animals given many conditioning trials with weak shock was CS specific. Collectively, these findings indicate that the malleability of learned behavior is not simply a function of initial associative strength but is dependent on path during initial acquisition.     

Stimulus intensity,catch trial effects,and the speed-accuracy tradeoff in reaction time: A variable criterion theory interptation

Ss responded to a 1,000-Hz tone of 50, 80, or 100 dB. Catch trial conditions were none, blank trials, a red light, a noise, and an 1,800-Hz tone. Auditory catch signals were of the same intensities. RT distributions in the first three conditions were well described by a family of exponential growth functions dependent upon stimulus intensity and by the parameters of normal criterion distributions dependent upon catch trial conditions and between-session variability. Performance in the auditory catch trial conditions was not dependent upon the same set of sensory growth functions. Performance in these conditions was described by a two-dimensional analysis of information transmitted as a function of time and interpreted in terms of variable criterion theory. The speed-accuracy tradeoff in this situation appears to depend upon differential rates of growth of intensity and associative information and the criterion used in responding to this information.