Neural correlates of partial transmission of sensorimotor information in the cerebral cortex

Using single neuron recordings in monkey primary motor (MI) cortex, two series of experiments were conducted in order to know whether response preparation can begin before perceptual processing finishes, thus providing evidence for a temporal overlap of perceptual and motor processes.

In Experiment 1, a “left/right, Go/No-Go” reaction time (RT) task was used. One monkey was trained to perform wrist flexion/extension movements to align a pointer with visual targets. The visual display was organized to provide a two-dimensional stimulus: side (an easy discrimination between left and right targets) which determined movement direction, and distance (a difficult discrimination between distal and proximal targets) which determined whether or not the movement was to be made. Changes in neuronal activity, when they were time-locked to the stimulus, were almost similar in the Go and No-Go trials, and when they were time-locked to movement onset, were markedly reduced in No-Go as compared to Go trials.

In Experiment 2, a stimulus-response compatibility (SRC) task was used. Two monkeys were trained to align a pointer with visual targets, on either left or right. In the spatially “compatible” trials, they had to point at the stimulus position, whereas in the “incompatible” trials, they had to point at the target located in the opposite side. For 12.5% of neurons, changes in activity associated with incompatible trials looked like changes in activity associated with movements performed in the opposite direction during compatible trials, thus suggesting the hypothesis of an automatic activation of the congruent, but incorrect response.

Results of both experiments provide evidence for a partial transmission of information from visual to motor cortical areas: that is, in the No-Go trials of the first task, information about movement direction, before the decision to perform or not this movement was made, and, in the incompatible trials of the SRC task, information about the congruent, but incorrect response, before the incongruent, but correct response was programmed.     

Modulation of motor area activity during observation of unnatural body movements

We investigated the processes underlying stimulus-response compatibility by using a lateralized auditory stimulus in a simple and choice reaction time (RT) paradigm. Participants were asked to make either a left or right key lift in response to either a control (80 dB) or startling (124 dB) stimulus presented to either the left ear, right ear, or both ears. In the simple RT paradigm, we did not find a compatibility effect for either control or startle trials but did find a right-ear advantage which we attribute to anatomical asymmetry of auditory pathways. In the choice RT paradigm, we found compatibility effects for both startle and control trials as well a high incidence of error for contralateral stimulus-response mapping. We attribute these results to automatic activation of the ipsilateral response, which must then be inhibited prior to initiation of the correct response. The presence of compatibility effects for startle trials also suggest that similar pathways are being used to initiate movements in a choice RT situation, as opposed to involuntary triggering that is thought to occur in a simple RT situation.     

Anticipatory response control in motor sequence learning: evidence from stimulus-response compatibility

Three experiments using a serial four-choice reaction-time (RT) task explored the interaction of sequence learning and stimulus-based response conflict. In Experiment 1, the spatial stimulus-response (S-R) mapping was manipulated between participants. Incompatible S-R mappings produced much higher RTs than the compatible mapping, but sequence learning decreased this S-R compatibility effect. In Experiment 2, the spatial stimulus feature was made task-irrelevant by assigning responses to symbols that were presented at unpredictable locations. The data indicated a Simon effect (i.e., increased RT when irrelevant stimulus location is spatially incompatible with response location) that was reduced by sequence learning. However, this effect was observed only in participants who developed an explicit sequence representation. Experiment 3 replicated this learning-based modulation of the Simon effect using explicit sequence-learning instructions. Taken together, the data support the notion that explicit sequence learning can lead to motor 'chunking', so that pre-planned response sequences are shielded from conflicting stimulus information.     

Temporal properties of human information processing: Tests of discrete versus continuous models

Cognitive psychologists have characterized the temporal properties of human information processing in terms of discrete and continuous models. Discrete models postulate that component mental processes transmit a finite number of intermittent outputs (quanta) of information over time, whereas continuous models postulate that information is transmitted in a gradual fashion. These postulates may be tested by using an adaptive response-priming procedure and analysis of reaction-time mixture distributions. Three experiments based on this procedure and analysis are reported. The experiments involved varying the temporal interval between the onsets of a prime stimulus and a subsequent test stimulus to which a response had to be made. Reaction time was measured as a function of the duration of the priming interval and the type of prime stimulus. Discrete models predict that manipulations of the priming interval should yield a family of reaction-time mixture distributions formed from a finite number of underlying basis distributions, corresponding to distinct preparatory states. Continuous models make a different prediction. Goodness-of-fit tests between these predictions and the data supported either the discrete or the continuous models, depending on the nature of the stimuli and responses being used. When there were only two alternative responses and the stimulus-response mapping was a compatible one, discrete models with two or three states of preparation fit the results best. For larger response sets with an incompatible stimulus-response mapping, a continuous model fit some of the data better. These results are relevant to the interpretation of reaction-time data in a variety of contexts and to the analysis of speed-accuracy trade-offs in mental processes.     

Partial advance information,number of alternatives,and motor processes: an electromyographic study

We present evidence that advance information reducing the number of stimulus-response alternatives in a choice reaction time (RT) task can shorten the very latest motoric stages of RT. Effects of such advance information on late stages of RT have been demonstrated recently by Osman, Moore, and Ulrich (Acta Psychol. 90 (1995) 111), Leuthold, Sommer, and Ulrich (J. Exp. Psychol: Gen. 125 (1996) 307), Müller-Gethmann, Rinkenauer, Stahl, and Ulrich (Psychophysiology 37 (2000) 507). These studies found that advance information shortens the portion of the RT interval following onset of a movement-related brain potential (lateralized readiness potential). Osman et al. and Müller-Gethmann et al. also examined the portion of the RT interval following the start of electromyographic (EMG) activity and found no effect of advance information. Based on Osman et al.'s null result, Leuthold et al. speculated that advance information may shorten only the RT stages preceding EMG activity. This conclusion, however, is questionable because of limitations in the EMG measures employed by both Osman et al. and Müller-Gethmann et al. We have reanalyzed the results of a previously reported experiment (Acta Psychol. 101 (1999) 243) to show that advance information can in fact affect the rate of recruitment of motor units in the prime mover of the responding limb.     

Dissociating automatic and controlled processes in a memory-search task: Beyond implicit memory

Our goal in this paper was to examine the processes that give rise to action slips. Procedures used to examine implicit memory and automatic processes were found to be unsatisfactory. However, the process-dissociation procedure proved useful for examining the contribution of the automatic and controlled processes underlying performance. The procedure was used in conjunction with a Sternberg memory-search task to examine the effects of set size, response speed, and stimulus-response mapping on controlled and automatic processes. The formulation allowed us to predict accurately how subjects would perform in a varied mapping condition. Moreover, set size and response speed were found to influence the controlled search process, but to leave the automatic influences unaffected. Stimulus-response mapping, on the other hand, was found to lead to probability matching in the automatic processes; this pattern was found to remain constant across changes in set size and response speed.     

An additive factor analysis of the effect of depression on the reaction time of old patients

Depressed participants display longer reaction times (RTs) than control participants. The present study was aimed at deciphering which stages of processing are affected by depression in old adults. Sixteen old depressed patients and 16 old healthy volunteers performed a two-choice visual RT task. Signal intensity, stimulus-response mapping and foreperiod duration were manipulated so as to affect the stages of stimulus preprocessing, response selection and motor adjustment, respectively. Reaction time data suggest that depression spares the stage of stimulus preprocessing but affects the stage of motor adjustment. An analysis of the error rate leaves open the possibility that depression alters the stage of response selection.     

Locus of the intensity effect in simple reaction time tasks

Evidence is still inconclusive regarding the locus of the stimulus intensity effect on information processing in reaction tasks. Miller, Ulrich, and Rinkenauer (1999) addressed this question by assessing the intensity effect on stimulus- and response-locked lateralized readiness potentials (LRPs) as indices of the sensory and motor parts of reaction time (RT). In the case of visual stimuli, they observed that application of brighter stimuli resulted in a shortening of RT and stimulus-locked LRP (S-LRP), but not of response-locked LRP (R-LRP). The results for auditory stimuli, however, were unclear. In spite of a clear RT reduction due to increased loudness, neither S-LRP nor R-LRP onset was affected. A reason for this failure might have been a relatively small range of intensity variation and the type of task. To check for this possibility, we performed three experiments in which broader ranges of stimulus intensities and simple, rather than choice, response tasks were used. Although the intensity effect on the R-LRP was negligible, S-LRP followed RT changes, irrespective of stimulus modality. These findings support the conclusion that stimulus intensity exerts its effect before the start of motoric processes. Finally, S-LRP and R-LRP findings are discussed within a broader information-processing perspective to check the validity of the claim that S-LRP and R-LRP can, indeed, be considered as pure estimates of the duration of sensory and motor processes.     

Advanced information about target location facilitates movement planning: More evidence using a deadline procedure on movement time

It was recently shown that in a multiple choice aiming task the knowledge of the target location prior to stimulus introduction, even though the trajectory to follow was still uncertain, facilitated movement planning and execution (Girouard et al. 1987). In that particular study, the subjects had, in the first condition, knowledge about the target location prior to the stimulus presentation. In that condition, they started their movements in the direction indicated by one of four possible stimuli. However, they always ended their movements on the same target (single-target condition). In a second condition, there was always a one-to-one mapping between the stimuli and the targets (multiple-target condition). The facilitating effects of knowing target location were found for both the movement planning time or reaction time (RT) and movement time (MT). A possible explanation of the latter effect was that the subjects, somewhere along the movement path, made a check to see if their movement was carried out as expected and corrected it accordingly. The purpose of the present experiment was to see if knowing the target to reach before the stimulus presentation, even though the trajectory to follow is uncertain, could override the well-known effect of stimulus-response uncertainty on RT (Hick 1952) when the possibility of making a check during MT was reduced. To reach that goal the methodology used by Girouard et al. (1987) was modified by limiting the time permitted to execute the required response. The effect of this manipulation was that it almost tripled the target location effect on RT found in the previous study. Furthermore, the significant effect found on MT disappeared for the single-target condition whilst it remained significant for the multiple-target condition. Different interpretations are offered to take into account the latter result.     

Age-related differences in reaction time task performance in young children

Performance of reaction time (RT) tasks was investigated in young children and adults to test the hypothesis that age-related differences in processing speed supersede a “global” mechanism and are a function of specific differences in task demands and processing requirements. The sample consisted of 54 4-year-olds, 53 5-year-olds, 59 6-year-olds, and 35 adults from Russia. Using the regression approach pioneered by Brinley and the transformation method proposed by Madden and colleagues and Ridderinkhoff and van der Molen, age-related differences in processing speed differed among RT tasks with varying demands. In particular, RTs differed between children and adults on tasks that required response suppression, discrimination of color or spatial orientation, reversal of contingencies of previously learned stimulus-response rules, and greater stimulus-response complexity. Relative costs of these RT task differences were larger than predicted by the global difference hypothesis except for response suppression. Among young children, age-related differences larger than predicted by the global difference hypothesis were evident when tasks required color or spatial orientation discrimination and stimulus-response rule complexity, but not for response suppression or reversal of stimulus-response contingencies. Process-specific, age-related differences in processing speed that support heterochronicity of brain development during childhood were revealed.     

The role of response selection in sequence learning

We investigated the role of response selection in sequence learning in the serial reaction time (SRT) task, by manipulating stimulus-response compatibility. Under conditions in which other types of learning, like perceptual, response-based, and response-effect learning, were unaffected, sequence learning was better with an incompatible than with a compatible stimulus-response mapping. Stimulus discriminability, on the other hand, had no influence on the amount of sequence learning. This indicates that the compatibility effects cannot be accounted for by a different level of task difficulty. Relating our results to the dimensional overlap model (Kornblum, Hasbroucq, & Osman, 1990), which assumes that incompatible stimulus-response mappings require more controlled response selection than do compatible stimulus-response mapping, we suggest that sequence learning in the SRT task is particularly effective when response selection occurs in a controlled way.     

Control over speeded actions: a common processing locus for micro- and macro-trade-offs?

Cognitive control processes associated with long- and short-term adjustments of human behaviour have attracted much interest recently. It is still unclear, however, whether the mechanisms underlying these adjustments share a common locus within the chain of stimulus-response processing. In order to address this issue, the present study employed a speed-accuracy instruction producing a macro-trade-off, whereas micro-trade-off was studied by means of posterror slowing in reaction time (RT). Participants performed a spatially compatible or incompatible four-stimuli-to-two-response alternative choice RT task. Reliable variations in micro-and macro-trade-off as well as effects of spatial compatibility were found in RT and error rate. Most importantly, posterror slowing was larger when instruction stressed accuracy rather than speed, an effect being independent of spatial compatibility. Because the influence of speed-accuracy instruction and posterror slowing on performance was strongest for response alternations, together present findings suggest that the mechanisms underlying micro- and macro-trade-offs have one common locus at the level of motor processing. Additional influences of macro-trade-off on premotoric processing are likely.     

Effect of prior practice on the stimulus-response compatibility effect in a mixed mapping environment

A stimulus-response compatibility (SRC) effect is obtained when performance is better with compatible mappings than with incompatible mappings. When mappings are mixed within a task, the SRC effect is often eliminated or reversed.The present study examines how 1,600 trials with different practice tasks can affect the response selection process in these mixed mapping environments. Participants were assigned to one of three practice groups: mixed mapping, pure compatible mapping, and pure incompatible mapping. Subsequently, all participants performed an experimental session in which compatible and incompatible trials were mixed.The SRC effect was eliminated in the experimental mixed mapping session, regardless of practice condition. The results suggest that practice does not change the need to suppress the direct response selection route in a mixed mapping task. However, reaction time distributions and sequential analyses were modulated by practice condition, which indicates that the new associations acquired during practice may activate new routes that interact with preexisting ones.     

The Simon effect for vertical S–R relations: changing the mechanism by randomly varying the S–R mapping rule?

Recent findings indicate that the shape of the effect function of the Simon effect--derived by analysing the response time distribution for corresponding and non-corresponding trials--differs depending on the task. Specifically, decreasing effect functions have been reported for horizontal and stable rather increasing effect functions have been obtained for vertical stimulus-response (S-R) relations. Furthermore, it has been assumed that these differences reflect distinct mechanisms underlying the Simon effect. However, in two studies decreasing effect functions were reported for the vertical dimension. In order to investigate these contradictory findings four experiments were conducted. Since both studies--in which a decreasing effect function was obtained--used a modified version of the Simon task, that is, randomly varying S-R mapping rules, the Simon effect for fixed and random S-R mapping rules was investigated using vertical (Experiments 1, 2, and 4) and horizontal (Experiment 3) S-R relations. The results indicate that randomly varying S-R mapping rules affect the shape of the effect function for vertical but not for horizontal S-R relations. It was concluded that these findings indicate that the alternation of S-R mapping rules changes the information processing for the vertical dimension in a way, that the same mechanism as for horizontal S-R relations occurs.     

Alternate response preparation in a visuomotor serial task

The preparation of a particular motor pattern is related to the information available that enables the actor to predict the correct response to a forthcoming stimulus. In many situations, however, prediction is not possible. In such cases, the individual can guess the probable parameters of the next stimulus. The authors attempted to establish the bias in the motor intention for movement and its interaction with a possible memory trace of the stimulus-response mapping produced by the preceding stimulus. Two letters were presented bilaterally, and participants (N=21) had to discriminate the target letter and respond with the compatible hand. The present findings support the existence of a memory trace of the previous stimulus-response mapping.     

Mechanisms of Priming by Masked Stimuli: Inferences From Event-Related Brain Potentials

A metacontrast procedure was combined with the recording of event-related potentials (ERPs) to examine the mechanisms underlying the priming effect exerted by masked visual stimuli (primes) on target processing. Participants performed spatially arranged choice responses to stimulus locations. The relationship between prime and target locations (congruity) and the mapping between target and response locations (compatibility) were factorially manipulated. Although participants were unaware of prime locations, choice responses were faster for congruent than incongruent conditions irrespective of the mapping. Visual ERP components and the onset of the lateralized readiness potential (LRP), an index of specific motor activation, revealed that neither perceptual nor preselection processes contributed to the congruity effect. However, the LRP waveform indicated that primes activated responses that fit the stimulus-response mapping. These results support the view that sensorimotor processing of masked stimuli is functionally distinct from their conscious perception.     

Stimulus-response compatibility and response preparation: effects on motor component of information processing for upper and lower limb responses

The effects of stimulus-response compatibility and response preparation on the motor component of the information processing system were investigated by analyzing the fractionated reaction time for the upper and lower limbs. The reaction time was divided into two periods with respect to the onset of electromyographic activity, premotor and motor times. The response preparation was manipulated by the probability that the locations of the precue and subsequent imperative stimulus corresponded. On a stimulus-response compatible task, subjects were required to release a key on the same side as an imperative stimulus, irrespective of the precued side. On an incompatible task, subjects were required to act in the reverse manner. The upper and lower limb responses were measured during both tasks. A repeated-measures design was used with 12 male university students. Analysis of the reaction and premotor times indicated that the stimulus-response compatibility effect became larger as response preparation decreased. The analysis of motor time yielded significant interactions between stimulus-response compatibility and limb and between response preparation and limb. These findings indicated that the motor component of information processing for the lower limb response is affected by both stimulus-response compatibility and response preparation.     

The effect of visual search efficiency on response preparation: neurophysiological evidence for discrete flow

Most models assume that response time (RT) comprises the time required for successive processing stages, but they disagree about whether information is transmitted continuously or discretely between stages. We tested these alternative hypotheses by measuring when movement-related activity began in the frontal eye field (FEF) of macaque monkeys performing visual search. Previous work showed that RT was longer when visual neurons in FEF took longer to select the target, a finding consistent with prolonged perceptual processing during less efficient search. We now report that the buildup of saccadic movement-related activity in FEF is delayed in inefficient visual search. Variability in the delay of movement-related activity accounted for the difference in RT between search conditions and for the variability of RT within conditions. These findings provide neurophysiological support for the hypothesis that information is transmitted discretely between perceptual and response stages of processing during visual search.     

Impairment of executive functions in boys with attention deficit/hyperactivity disorder.

The main aim of the present study is to compare the efficiency of executive control processes in 24 boys with attention deficit/hyperactivity disorder (ADHD) and 58 normal controls of similar age (between 8 and 11 years). Three reaction time (RT) paradigms were utilized: a dual task that requires coordination of two tasks responses, a shift task that makes it necessary to disengage attention from one task and engage into another one, and a stimulus-response spatial compatibility task that requires participants to inhibit a prepotent response. Another purpose of the study is to examine whether Barkley's (1997) executive dysfunction or Sergeant et al.'s (1999) resource allocation/arousal model best account for the behavioral deficits associated with ADHD. Examination of raw RT data showed significantly poorer performance in ADHD children with respect to age-matched controls on both the higher-level cognitive functions of executive control and on lower-level abilities (e.g., speed of processing) of all tasks of this study. However, using proportional transformations of raw RT data, we could demonstrate that, in addition to differences in processing speed, also executive control processes were significantly impaired in children with ADHD.     

Response preparation and stimulus-response congruence to fractionating reaction time of upper and lower limbs

We measured the fractionating reaction time for upper and lower limbs of 18 young men, using an electromyogram to clarify the interaction of response preparation and stimulus-response congruence on premotor and motor time. The reaction time was divided into two periods with respect to the onset of the electromyogram, premotor and motor components. Manipulating the probability of the Go versus NoGo signals varied three different amounts of response preparation. Prior to the imperative stimulus, precue information about the position of a stimulus was presented. In the stimulus-response congruent task, subjects were required to release a key on the same side of the body using either an upper or lower limb in response to an imperative Go stimulus. In the stimulus-response incongruent task, subjects were required to act in a reverse manner. Subjects were not supposed to respond to the NoGo stimulus. The premotor time of the upper and lower limb responses was affected by the respective effects of response preparation and stimulus-response congruence. The motor time of the upper and lower limb responses increased as the probability of the Go signal decreased but not in relation to stimulus-response congruence. These results suggest that response preparation affects not only information processing time but also peripheral motor activity due to motor programming, and that the stimulus-response congruence effect on motor time disappears when information about the position of the imperative stimulus is precued.