Slow potential changes and choice reaction time as a function of interstimulus interval

Slow potential changes were recorded over the vertex (C_z) during a choice reaction task. The constant interstimulus interval (ISI) between the visual warning (S₁) and the visual imperative signal (S₂) was either 200, 400, 1000 or 2000 msec. The contingent negative variation (CNV) was not only measured between S₁ and S₂ (CNV₂), but also before S₁ (CNV₁).The main results were: (1) The CNV₂ amplitude showed significant variation as a function of ISI. It reached its maximum with an ISI of 1000 msec. (2) CNV₁ developed only before the short ISIs (200 and 400 msec). (3) When CNV₁ and CNV₂ were summed the differences in CNV amplitudes and durations between different ISIs became smaller. (4) The peak-to-peak amplitude P₁-N₁ of the potential evoked by S₁ was enhanced with short ISIs. (5) The correlations between mean CNV and median reaction time (RT) were low but significant for ISIs of 400, 1000 and 2000 msec. When, however, the effect of subjects was partialized out these correlations were drastically reduced, whereas the partialization of session and block effects had no noticeable influence on these correlations. (6) The correlations between single RT and single CNV (measured for the ISI of 1000 msec, individually for two subjects) were weak or even completely lacking.The main conclusion was that CNV coincides with preparedness to react to a stimulus in a choice RT-task, but its amplitude at the moment of onset of the imperative stimulus does not reflect, or reflects weakly, the degree of preparedness (as indicated by RTs) at that moment.     

Effects of time and event uncertainty upon sequential information processing

Two experiments were conducted to investigate the psychological refractory period (PRP), a delay induced into the second of two reaction times (RT) when the interstimulus interval (ISI) is short. In Experiment1, time and event uncertainty were factorially varied by providing or not providing S with foreknowledge of the ISI and the order in which the two events would occur, respectively. ISIs of0, 50, 100, 200, and400 msec were used. Time and event uncertainty produced independent degradation of both RTs. Also, the second RT (RT ₂ ) was delayed at50 msec ISI when both time and event certainty were present. Experiment 2 attempted to replicate this latter finding using ISIs of0, 25, 50, 75, and100 msec. Delays in RT ₂ were found for the middle three values of ISI. These results were interpreted as supporting a modified single channel theory of the PRP.     

Effects of Prime Type and Delay on Multiplication Priming: Evidence for a Dual-process Model

Two experiments investigated effects of numerical primes on production of simple multiplication facts (e.g. 4 × 8 = ?). In Experiment 1, a correct (32), related (24), unrelated (27), or neutral (##) prime appeared for 200 msec and was followed by a target problem at an ISI of 0, 750, or 1500 msec. Relative to neutral primes, correct primes produced constant RT and accuracy benefits across ISIs, and unrelated primes produced constant RT costs. Related primes produced costs compared to unrelated primes at the 0-msec ISI only. In Experiment 2, eliminating correct-answer primes from the stimulus set eliminated all the false-prime effects except the costs of related primes at the 0-msec ISI. We propose a dual-process account incorporating a familiarity-based name-the-prime strategy that produces benefits and costs insensitive to ISI and an automatic retrieval-priming process that is measurable only at short ISIs.     

Parameters affecting gap detection in the rat

The present research used a startle amplitude reduction paradigm to investigate the ability of the rat’s auditory system to track rapidly changing acoustic transients. Specifically examined was the ability of brief gaps in otherwise continuous noise to reduce the amplitude of a subsequently elicited acoustic startle reflex. The duration of the gap, time between gap offsetand startle elicitation (the interstimulus interval or ISI), and rise-fall characteristics of the gap were systematically varied. Consistent with previous research, gaps reliably reduced startle amplitude. Gaps 2 msec long were reliably detected, and a 50-msec ISI resulted in the greatest amplitude reduction. Gaps presented at short ISIs produced amplitude reduction that followed a different time course than did gaps presented at longer ISIs. These results may reflect differences in the length oftime available for the processing of the stimulus and may involve two different processes.     

The psychological refractory period and vertex evoked potentials

The averaged sensory evoked potential (EP) was recorded from the scalp (vertex to mastoid) in a psychological refractory period experiment in which 12 young adults participated. Reaction times (RTs) were measured to either both or only the second of pairs of stimuli, in different trial blocks, with inter-stimulus intervals (ISIs) of 100, 200, 300 and 400 msec occurring in random sequence. EPs were recorded at each ISI. No latency changes could be found in the prominent non-specific components (P1-N1-P2) of the EP to stimulus 2 even at ISIs where the RT was substantially delayed. Thus the notions that the RT2 delay is due to occupation of a single channel central processor by S1 and that non-specific EP components reflect the time course of information processing in underlying neural tissue, do not lend each other mutual support. Furthermore, as profound amplitude refractoriness in components P1-N1 and N1-P2 persisted at ISIs where RT was as fast or faster than simple RT, there appears to be a dissociation between “psychological refractoriness” and “physiological refractoriness”. The implications of these results are discussed.     

Auditory frequency discrimination in adult developmental dyslexics

Developmental dyslexics reportedly discriminate auditory frequency poorly. A recent study found no such deficit. Unlike its predecessors, however, it employed multiple exposures per trial to the standard stimulus. To investigate whether this affects frequency discrimination in dyslexics, a traditional two-interval same-different paradigm (2I_1A_X) and a variant with six A-stimuli per trial (2I_6A_X) were used here. Frequency varied around 500 Hz; interstimulus interval (ISI) ranged between 0 and 1,000 msec. Under 2I_1A_X, dyslexics always had larger just noticeable differences (JNDs) than did controls. Dyslexic and control JNDs were equal at shorter ISIs under 2I_6A_X, but dyslexics became worse than controls at longer ISIs. Signal detection analysis suggests that both sensory variance and trace variance are larger in dyslexics than in controls.     

Nonselective read-out from iconic memory in normal, borderline and retarded adolescents

The hypothesis that retarded individuals read-out information from iconic memory at a slower rate, relative to their CA matched peers, was tested. Three IQ groups (normal, borderline and retarded) were selected with 10 subjects in each group. A tachistoscope presented a stimulus array and a post-stimulus cue for 100 msec. each, separated by a variable interstimulus interval (ISI). This stimulus array consisted of 10 letters arranged on two horizontal rows. The post-stimulus cue was a circle which surrounded the position of the correct letter. Nine ISIs were used and ranged from −100 (cue before array) to 500 msec. A 3 × 9 repeated-measures analysis of variance revealed non-significant effects for IQ and the IQ × ISI interaction. A significant effect was found for ISIs (p < .01) which reflected reduced performance at the intermediate ISIs for all intelligence groups. The hypothesis of a read-out deficit in the retarded was not supported. The present findings were discussed in relation to previous research which supported a read-out deficit in the retarded.     

Discrimination learning as a function of stimulus location along an auditory intensity continuum

Eight groups of rats were trained on an auditory intensity discrimination in which the discriminative stimuli were separated by 10 decibels (db). Four pairs of stimuli were selected from different regions along a 60–100 db (SPL) intensity continuum. Counterpart groups were trained on each stimulus pair, with the relative intensity positions of the reinforced stimulus (S^D) and the non-reinforced stimulus (S^Δ) reversed for the two groups. Discrimination acquisition curves were compared to determine whether stimuli separated by equal logarithmic units were of comparable “difficulty”, and to determine the relative effectiveness of an S^D serving as the more versus less intense member of a stimulus pair. It was concluded that: (1) When S^D is the more intense, auditory intensities of constant logarithmic separation are graded in “difficulty” along the intensity continuum; high intensity discriminative stimuli are most readily discriminated. When S^Δ is the more intense, this graded effect is not evident. (2) For a given continuum location, discrimination is inferior when S^Δ is the more intense. This effect is most pronounced at the high intensity end of the continuum and is chiefly attributable to differences in the rate of S^Δ responding.     

Cardiac modulation of startle: Effects on eye blink and higher cognitive processing

Cardiac cycle time has been shown to affect pre-attentive brainstem startle processes, such as the magnitude of acoustically evoked reflexive startle eye blinks. These effects were attributed to baro-afferent feedback mechanisms. However, it remains unclear whether cardiac cycle time plays a role in higher startle-related cognitive processes, as well. Twenty-five volunteers responded first by ’fast as possible’ button pushes (reaction time, RT), and second, rated perceived intensity of 60 acoustic startle stimuli (85, 95, or 105 dB; 50 ms duration; binaural; instantaneous rise time), which were presented either 230 or 530 ms after the R-wave, and eye blink responses were measured by EMG. RT was divided into evaluation and motor response time according to previous research. Increasing stimulus intensity enhanced startle eye blink, intensity ratings, and RT components. Eye blinks and intensity judgments were lower when startle was elicited at a latency of R + 230 ms, but RT components were differentially affected: the evaluative component was attenuated, and the motor component was accelerated when stimuli were presented 230 ms after the R-wave. We conclude that the cardiac cycle affects the attentive processing of acoustic startle stimuli.     

Timing in trace conditioning of the nictitating membrane response of the rabbit (Oryctolagus cuniculus): scalar, nonscalar, and adaptive features

Using interstimulus intervals (ISIs) of 125, 250, and 500 msec in trace conditioning of the rabbit nictitating membrane response, the offset times and durations of conditioned responses (CRs) were collected along with onset and peak latencies. All measures were proportional to the ISI, but only onset and peak latencies conformed to the criterion for scalar timing. Regarding the CR's possible protective overlap of the unconditioned stimulus (US), CR duration increased with ISI, while the peak's alignment with the US declined. Implications for models of timing and CR adaptiveness are discussed.     

Common response processing and psychological refractoriness

This experiment examined whether structural considerations, that is the functional closeness of limb control centres (Kinsbourne and Hicks 1978), have a role to play in common processing models of psychological refractoriness. A typical double stimulation paradigm was used (Kantowitz 1974). On experimental trials, subjects responded with the right hand (RT1) to an auditory signal (0.80 probability). After a varied interstimulus interval (ISI) of 100, 200, 300 or 700 msec, one of three lights corresponding to one of the other limbs provided the signal for the second response (RT2). Control trials for RT1 and RT2 involved both stimuli, but subjects were required to make only one response. Results indicated that experimental RT1 was lengthened considerably over control values. While typical double stimulation effects were found at short ISIs, that is RT2 was lengthened, RT2 at long ISIs was actually faster than double stimulation control values. Although the RT results were not in a pattern that would be predicted by functional distance (Kinsbourne and Hicks 1978), within subject correlations of RT1 and RT2 by limb condition suggest that structural considerations may have a role to play. While within subject correlations were positive at all levels of ISI, they decreased as the interval between the two signals increased. The implications of these results for common processing models are discussed.     

Antecedent reinforcement contingencies in the stimulus control of an auditory discrimination

In order to assess possible confounding of discriminative stimulus effects with those produced by the reinforcing stimulus, three groups of four rats each were trained for 45 hr on a variable-interval 1-min reinforcement program. Two groups were run on a multiple variable-interval extinction schedule in which the reinforcement stimulus (S^D) and the nonreinforcement stimulus (S^Δ) were two intensities of a 4-kHz (cps) tone separated by 40 or 10 db. The third group was run on a mixed schedule with a single intensity constantly present. The mixed-schedule animals showed no discrimination of the reinforcement program. Under the multiple schedule, the highest S^Δ rates were obtained after S^D intervals, regardless of the reinforcement availability in the S^D interval. These local rate variations in S^Δ were small in proportion to those produced by the S^D versus S^Δ intensities.     

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.     

EFFECTS OF INTERSTIMULUS INTERVAL AND PREDICTABILITY OF EVENT STRUCTURE ON SERIAL REACTION TIME

A mean interstimulus interval (ISI) of 10 sec. resulted in significantly-shorter RTs to a single light stimulus than a 30 sec. average ISI. During a second workperiod the groups performing under each of the two ISI conditions were divided into four subgroups given 0, 25, 50 or 75% interspersion of an additional stimulus (sound). With short ISIs the condition of maximum predictability of event structure (light stimulus only) gave the shortest average RTs. With lessened predictability (increased proportion of the sound stimulus) there was a slight monotonous increase in RT. With long ISIs the same relationship was curvilinear, i.e. 25% interspersion of sound stimulus was most effective in preserving vigilance.     

Modification of the rat's acoustic startle response by antecedent visual stimulation.

Male hooded and albino rats were exposed to a light flash followed at various temporal intervals by a startle-eliciting 117 db. (re 20 muN/m2) burst of white noise. The visual stimulus engendered startle response inhibition (maximally when the lead time was 64-250 msec) as well as startle response latency reduction (maximally when the lead time was 2-8 msec). The temporal functions for the effects of visual stimuli paralleled those previously reported for startle modification by acoustic events. Further study revealed that, given optimal lead times, inhibition is produced reliably by weaker visual stimuli (3 X 10-6 cd-sec/cm2) than latency reduction (3 X 10-4 cd-sec/cm2). This differential sensitivity to visual stimuli is also analogous to previously reported findings for events in the acoustic environment. It reveals that the neural mechanisms that mediate latency reduction and inhibition can be engaged by either acoustic or visual stimulation.     

Effects of time-order, interstimulus interval, and feedback in duration discrimination of noise bursts in the 50- and 1000-ms ranges

Participants compared durations of paired white-noise bursts, with interstimulus interval (ISI) 100, 300, 900, or 2700 ms, presented in the order standard (St)-comparison (Co) or Co-St. St was 50 or 1000 ms, and 75% difference thresholds for "longer" and "shorter" judgments were estimated. In Experiment 1 feedback was given; in Experiment 2, with ISIs 900 and 2700 ms, there was no feedback. For St=1000 ms, the just noticeable difference (JND) in noise duration was generally smaller with the order St-Co than with Co-St; for St=50 ms, the JND relation was the opposite. JNDs increased with shorter ISIs. Time-order errors were positive for St=50 ms and negative for St=1000 ms, and approached zero for longer ISIs. Using Hellstr?m's sensation-weighting (SW) model, the ratio of the stimulus weights for the first and second burst was estimated; this ratio was generally >1 for St=50 ms and <1 for St=1000 ms. JNDs were smaller with feedback than without; the greatest reduction was found for St=1000 ms and an ISI of 2700 ms with the order Co-St, possibly because feedback increased participants' attention to the first stimulus. These results demonstrate the sensitivity of discrimination measures for long as well as brief durations to the factors of ISI, presentation order, and feedback. They also suggest different modes of stimulus processing for short and long durations.     

The effect of frequency variation upon RT to the second of two shortly spaced auditory stimuli

A prepulse of a duration of 25 msec (S₁) was followed by an auditory reaction stimulus (S₂) requiring a binary choice.     

Visual form recognition threshold and the psychological refractory period

Two experiments studied the effect of a reaction time response (RT) on visual form recognition threshold when the temporal interval separating the RT stimulus and the recognition stimulus was short. In Experiment 1 an initial RT response to an auditory signal did not impair the subsequent forced-choice visual form recognition threshold. Interstimulus intervals (ISI) of 0, 50, 100, 150, and 200 msec were used; S was always aware of the ISI under test. In Experiment 2 a visual stimulus was used to elicit the R T response; this shift to an intramodal stimulus did not alter the recognition threshold. These data were interpreted as supporting the hypothesis that two stimulus events can be processed simultaneously even when the temporal interval between them is short.     

Effect of the length of the runs of repetitions on the simple RT-ISI relationship

In a simple RT task the temporal organization of the preparatory processes during a given trial depends upon the time characteristics of the total experimental situation as well as upon the information gathered during one or more previous trials. The present experiment was run in order to determine whether or not these long and short term effects operate independently or interact. The effects of the preceding ISI durations on the simple RT for an ISI 1 (1.5 s) or an ISI 2 (3.0 s) are analysed in 3 experimental conditions differing in the maximum number of successive repetitions (2, 3 or 7) of trials with the same ISI. The results show that the distribution of the preparatory activity during a given trial depends firstly on the number of successive ISIs of the same duration preceding this trial, and secondly on the maximum number of repetitions. An explanation of the subjects' strategy based upon “cost of preparation” is proposed.     

Intersensory effects in the psychological refractory period

Two experiments examined reaction time (RT) to each of two stimulus events separated by short interstimulus intervals (1SI). The essential contrast was RT to the second visual signal, RT₂, in auditory-visual (A-V) vs visual-visual (V-V) sequences. With response, certain pairings in Experiment 1, an effect apparently demonstrating a single-channel process (Welford, 1952), was noted. RT₂ was generally faster for A-V as opposed to V-V sequences especially when Ss were uncertain as to the sequence that would occur. At 0-msec ISI, the RT₂ difference between sequences approached the RT! difference. More rapid RT₂ to A-V sequences was also observed with go vs no-go pairings in Experiment 2 when the initial event was a go signal. However, the RT difference disappeared upon error correction, making the RT₂ sequence difference of questionable relevance to the hypothetical single-channel process. RT₂ was more rapid following a null no-go signal when the no-go signal was contrasted with a visual as opposed to auditory go signal. The latter effect was independent of error and is consistent with channel-switching theory (Kristofferson, 1967).