Contrast effects on the auditory evoked response and its relation to psychophysical judgments

An auditory average evoked response (AER) procedure was used to search for a physiological counterpart of the contrast effect-the tendency for a S’s judgment of the intensity of a stimulus to be modified by the intensity of prior stimulation. When a tone was preceded by a softer tone, its AER amplitude increased; conversely, when a tone followed a louder tone, amplitude decreased. Irregular intervals between tones decreased the AER contrast effect, as did increasing the interval between tones. Further, significant correlations were found between individual scores on the AER contrast procedure and performance on a battery of psychophysical tasks.     

Extraversion and the effects of frequency and intensity on the auditory brainstem evoked response

Extraversion was positively correlated with the latency of wave I of the auditory brainstem evoked response (BER) at 75, 80 and 85 dB of intensity. Extraverts also tended to display longer latency for wave V than introverts to high frequency, 80-dB tone bursts and to click stimuli at intensity levels which ranged from 55 to 85 dB (SPL). These results are consistent with reports of greater auditory sensitivity (d') and enhanced amplitude of the late (N₁–P₂) cortical evoked response for introverts. The absence of differences in interpeak latency, or central transmission time. center the effects on wave I which is thought to be generated by the cochlear nerve. The present findings may require the elaboration of the neurophysiological bases of extraversion, which presently focuses on differences in cortico-reticular arousal systems, to accomodate individual differences in axonal or synaptic transmission.     

Spatial summation in the evoked cortical response to auditory stimuli

Six Ss were presented monaurally and binaurally with stimuli of 0.5, 2.0, and 4.0 kHz at 40 and 70 dB sensation levels. Their computer averaged evoked potentials indicated substantially larger amplitudes (N₁ -P₂) with bilateral stimulation, regardless of frequency. Stimulation at 70 dB SL gave greater responses than that to 40 dB.     

A comparison of chinchilla auditory evoked response and behavioral response thresholds

The auditory sensitivity of the chinchilla was measured by both a behavioral and auditory evoked-response (AER) procedure. There was no significant difference in either the waveform or the threshold of the AER recorded over the tentorium from awake and anesthetized chinchillas. The chinchilla threshold for pure tones appears to be more sensitive when measured by the behavioral technique than by the AER method. Both the AER and behavioral response of three chinchillas exposed to a 105 dB SPL octave band of noise centered at 2 KHz for 3 h shifted markedly after the exposure. However, the difference between the AER and behavioral response threshold was reduced or absent. During the process of recovery the difference between the two responses begins to reappear.     

A simple stimulus generator for evoked response studies

An inexpensive computer-driven bipolar stimulator is described. The device produces variable-duration bipolar click stimuli for use in auditory evoked response studies, but is applicable to other research. The unit is driven directly from the digital input/output interface of the averaging computer, and temporal parameters are completely controlled by the machine.     

Extraversion, attention, and habituation of the auditory evoked response

Short-term changes in the auditory evoked response to low-frequency tones (0.5 kHz, 80 dB) were examined for independent groups of introverts and extraverts under attend and ignore conditions. Introverts displayed greater N1-P2 amplitude than extraverts to the first stimulus in a four-stimulus train. The N1-P2 amplitude differences between introverts and extraverts could not be attributed to differences between the groups in either habituation or attention processes. Overall, the effect is indicative of the introverts' enhanced sensitivity to physical stimulation.     

Saccade latency and warning signals: Effects of auditory and visual stimulus onset and offset

Previous studies have found that a nonspecific visual event occurring at the fovea 50–150 msec after the onset of a peripheral target delayed the initiation of the saccade to that target. The present studies replicated and extended this finding by studying the effects of both visual and auditory warning signals, by examining the effects of onset and offset warning on manual response latency, and by investigating the effects of presenting the warning events in the periphery of the visual field. The results indicated that the interfering effects occur with visual but not auditory stimuli, with saccades but not motor responses, and when the visual warning event occurs either foveally or in the subject’s periphery. Implications for the processes involved are discussed.     

Infant temperament and the brainstem auditory evoked response in later childhood.

Brainstem auditory evoked responses (BAERs) were evaluated on 10-12-year-old children (N = 56) who had been classified as high or low reactive to unfamiliar stimuli at 4 months of age. BAER measurement was selected because high reactive infants tend to become inhibited or fearful young children, and adult introverts have a faster latency to wave V of the BAER than do extroverts. Children previously classified as high reactive at 4 months had larger wave V components than did low reactive children, a finding that possibly suggests greater excitability in projections to the inferior colliculus. The fact that a fundamental feature of brainstem activity differentiated preadolescent children belonging to two early temperamental groups supports the value of gathering physiological data in temperament research.     

The influence of irrelevant stimulus changes on stimulus and response repetition effects

In this study the influence of irrelevant stimulus changes from one trial to another in a serial reaction time task was investigated. Two experiments were performed in which subjects were required to respond to stimulus colour. Four colours were mapped on two response keys, so that colour and response repetition effects could be dissociated. In Experiment 1, the irrelevant stimulus dimension was location and in Experiment 2 it was shape. Both experiments were performed with a short and a long response-stimulus interval (RSI)-condition. In both experiments, the irrelevant dimension influenced the response repetition effect but not the colour repetition effect. In the reaction times, a response alternation effect was observed only when the irrelevant location of the stimulus changed in the long RSI-condition. The error rates showed a response alternation benefit for both irrelevant dimensions, in the short and the long RSI-condition. The benefit for response alternations is explained in terms of a response bias towards change that is triggered by a changing stimulus feature. We assume that the response bias is stronger for location than for colour and that accuracy is more sensitive to this bias than response latencies.     

The relationship between latency of auditory evoked potentials,simple reaction time,and stimulus intensity

Summary The effects of loudness on the latency of evoked potentials and on simple reaction time were compared. It was found that both reaction time and the evoked-potential latency increases with decreasing stimulus intensity. However, different slopes of the curves were found. This is explained in terms of the arousal effect of loud auditory stimuli.     

Maximum-likelihood estimation of the accuracy of auditory discrimination in the absence of an overt response to every stimulus

In research on human performance in which techniques for estimating hits and false-alarm rates are used in conjunction with other measurements, such as evoked potentials, it is necessary to devise special data-collection methods. This paper describes such data-collection methods, together with a statistical method for summarizing the data. The statistical method consists of setting up a probability model whose parameters describe the process and then estimating the parameters using maximum likelihood.     

Compatibility effects based on stimulus and response numerosity

Four choice reaction time experiments documented a stimulus-response (S-R) compatibility effect involving the numbers of stimuli and responses. In Experiment 1, the stimulus consisted of one or two tones, and the correct response was either one or two taps of a response key. Responses were much faster with a compatible S-R assignment, in which the number of taps matched the number of tones, than with an incompatible assignment in which these numbers mismatched. Experiments 2 and 3 replicated this effect, using visual stimuli and bimodal stimuli, respectively, suggesting that auditory/manual rhythmic compatibility is not essential to it. Experiment 4 showed that an analogous but smaller effect is obtained when stimuli are the digits 1 and 2. This new numerosity-based compatibility effect has general theoretical implications regarding the mechanisms responsible for compatibility effects and practical implications for interface design.