What effect can rhythmic finger tapping have on the phonological similarity effect?

The effects of rhythmic finger tapping on the phonological similarity effect were investigated in two experiments. In both, subjects were tested for serial recall of visually presented letter sequences that were either phonologically similar or dissimilar. The letter sequences had to be remembered under three tapping conditions: right-hand tapping, left-hand tapping, and a no-tapping control. Experiment 1 showed clear phonological similarity effects in both the control and the left-hand tapping conditions, but not in the right-hand tapping condition, when recall responses were written with the right hand. When the number of tapping practice trials was fixed at two and recall was vocal in Experiment 2, the phonological similarity effect was eliminated in both the right-hand and the left-hand tapping conditions. These results suggest that some form of speech motor programs played an important role in serial recall.     

Memory drum theory: alternative tests and explanations for the complexity effects on simple reaction time

Two experiments investigated the memory drum theory's prediction (Henry & Rogers, 1960) that simple reaction time (SRT) increased with the complexity of the response to be initiated. Experiment 1 (N = 9) matched the Experiment 1, Group 1, SRT condition described by Henry and Rogers. Results of Experiment 1 replicated those of Henry and Rogers and indicated that the memory drum theory's prediction of increased SRT as a function of increased complexity of response was tenable. Experiment 2 (N = 11) tested the effects of anatomical unit, extent and target size on SRT, premotor time, and motor time. The results supported the contention that alternative explanations for SRT were possible. With complexity constant, increases in anatomical unit lead to increases in SRT, but only in the motor time component which indicated electromechanical rather than neuromotor program delays. It is proposed that the increased motor time could be explained by peripheral events such as the duration maximum torque must be applied by the agonist muscle(s) to generate the angular acceleration required to initiate rapid movement. SRT, premotor time, and motor time increased when target size was reduced from 6.35 cm to 79 cm. The increased premotor time could be a function of the determining of new equilibrium points for the elbow joint during response initiation. No effects on SRT were observed for extent.     

Control of goal-directed movements: the contribution of orienting of visual attention and motor preparation.

Three experiments investigated the role of attention and motor preparation for the control of goal-directed movements. In Experiment 1 (double step paradigm), a movement correction was required on 25% of the trials towards the left or right of the initial target. Within these 25% of trials, the probability of location of the second target was manipulated. The efficiency of movement control increased when increasing the probability of correcting the movement in a given direction. In Experiment 2, attentional processes were isolated by asking the subjects to verbally detect the more or less probable target displacement, without correcting their movement. Subjects were able to orient visual attention during movement execution, thus improving the processing of visual feedbacks from target displacement. In Experiment 3, motor preparation processes were isolated by asking the subjects to correct their movement towards a fixed target in response to a more or less probable mechanical perturbation. It was shown that motor preparation not only specifies the initial movement parameters but may also include some parameters of the most probable movement modulations. Overall, these results highlight the role of both attentional and motor preparation processes in the control of goal-directed movements and suggest that the feedback-based corrections of the movement are modulated by a feedforward control.     

The utilization of visual information in the control of rapid sequential aiming movements.

Two experiments were conducted to examine the role of vision in the execution of a movement sequence. Experiment 1 investigated whether individual components of a sequential movement are controlled together or separately. Participants executed a rapid aiming movement to two targets in sequence. A full vision condition was compared to a condition in which vision was eliminated while in contact with the first target. The size of the first target was constant, while the second target size was varied. Target size had an influence on movement time and peak velocity to the first target. Vision condition and target size did not affect the time spent on the first target. These results suggest that preparation of the second movement is completed before the first movement is terminated. Experiment 2 examined when this preparation occurred. A full vision condition was compared to a condition in which vision was occluded during the flight phase of the first movement. Movement initiation times were shorter when vision was continually available. Total movement time was reduced with vision in two-target condition, but not in a control one-target condition. The time spent on the first target was greater when vision was not available during the first movement component. The results indicate that vision prior to movement onset can be used to formulate a movement plan to both targets in the sequence [Fischman & Reeve (1992).     

Locus of inhibition in the masked priming of response alternatives

Masked prime stimuli presented immediately before target stimuli in a choice reaction task give rise to behavioral costs when the primes and the target stimuli are mapped to the same response and result in benefits when they are mapped to opposite responses. Researchers assume that this negative compatibility effect reflects inhibitory processes in the control of perceptuomotor links. The authors investigated whether the inhibition operates at the level of abstract central codes or at effector-specific motor stages. In 2 experiments (N = 8 participants in each), left or right hand or foot responses were required to target stimuli that were preceded by masked arrow primes mapped to the same response side as the target stimuli in compatible trials and to the opposite response side in incompatible trials; the primes were irrelevant in neutral trials. In Experiment 1, when the masked primes determined both response side and modality, there was no transfer of negative compatibility effects across response modalities. That finding is inconsistent with a central abstract locus of inhibition and suggests that inhibition operates at effector-specific motor stages. In Experiment 2, primes conveyed only response side information but left response modality uncertain, and negative compatibility effects were elicited for both hand and foot responses, suggesting that partially informative masked primes can trigger a parallel activation and subsequent inhibition of response processes within separate effector systems.     

The planning and execution of sequential eye movements: saccades do not show the one target advantage

The present experiment examined the one-target advantage (OTA) with regard to saccadic eye movements. The OTA, previously found with manual pointing responses, refers to the finding that movements are executed faster when the limb is allowed to stop on the target compared to the situation where it has to proceed and hit a second target. Using an adapted limb movement OTA task, saccades of 5 degrees and 15 degrees were made to (a) a single target (one-target), (b) one target and immediately to another target without a change in direction (two-target-extension), and (c) one target and immediately back to the start location (two-target-reversal). Unlike manual movements, the movement times for the initial saccade in the two-target-extension condition were not prolonged compared to either of the other two conditions. Moreover, this pattern of results was found for both the shorter and longer amplitude saccades. The results indicate that the OTA does not occur in the oculomotor system and therefore is not a general motor control phenomenon.     

Effects of referential ambiguity,time constraints and addressee orientation on the production of morphologically complex words

In five experiments, participants were asked to describe unambiguously a target picture in a picture–picture paradigm. In the same-category condition, target (e.g., water bucket) and distractor picture (e.g., ice bucket) had identical names when their preferred, morphologically simple, name was used (e.g., bucket). The ensuing lexical ambiguity could be resolved by compound use (e.g., water bucket). Simple names sufficed as means of specification in other conditions, with distractors identical to the target, completely unrelated, or geometric figures. With standard timing parameters, participants produced mainly ambiguous answers in Experiment 1. An increase in available processing time hardly improved unambiguous responding (Experiment 2). A referential communication instruction (Experiment 3) increased the number of compound responses considerably, but morphologically simple answers still prevailed. Unambiguous responses outweighed ambiguous ones in Experiment 4, when timing parameters were further relaxed. Finally, the requirement to name both objects resulted in a nearly perfect ambiguity resolution (Experiment 5). Together, the results showed that speakers overcome lexical ambiguity only when time permits, when an addressee perspective is given and, most importantly, when their own speech overtly signals the ambiguity.     

Memory Drum Theory

Two experiments investigated the memory drum theory’s prediction (Henry & Rogers, 1960) that simple reaction time (SRT) increased with the complexity of the response to be initiated. Experiment 1 (N = 9) matched the Experiment 1, Group 1, SRT condition described by Henry and Rogers. Results of Experiment 1 replicated those of Henry and Rogers and indicated that the memory drum theory’s prediction of increased SRT as a function of increased complexity of response was tenable. Experiment 2 (N = 11) tested the effects of anatomical unit, extent, and target size on SRT, premotor time, and motor time. The results supported the contention that alternative explanations for SRT were possible. With complexity constant, increases in anatomical unit lead to increases in SRT, but only in the motor time component which indicated electromechanical rather than neuromotor program delays. It is proposed that the increased motor time could be explained by peripheral events such as the duration maximum torque must be applied by the agonist muscle(s) to generate the angular acceleration required to initiate rapid movement. SRT, premotor time, and motor time increased when target size was reduced from 6.35 cm to .79 cm. The increased premotor time could be a function of the determining of new equilibrium points for the elbow joint during response initiation. No effects on SRT were observed for extent.     

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.     

Goal-driven modulation as a function of time in saccadic target selection

Four experiments were performed to investigate the contribution of goal-driven modulation in saccadic target selection as a function of time. Observers were required to make an eye movement to a prespecified target that was concurrently presented with multiple nontargets and possibly one distractor. Target and distractor were defined in different dimensions (orientation dimension and colour dimension in Experiment 1), or were both defined in the same dimension (i.e., both defined in the orientation dimension in Experiment 2, or both defined in the colour dimension in Experiments 3 and 4). The identities of target and distractor were switched over conditions. Speed–accuracy functions were computed to examine the full time course of selection in each condition. There were three major results. First, the ability to exert goal-driven control increased as a function of response latency. Second, this ability depended on the specific target–distractor combination, yet was not a function of whether target and distractor were defined within or across dimensions. Third, goal-driven control was available earlier when target and distractor were dissimilar than when they were similar. It was concluded that the influence of goal-driven control in visual selection is not all or none, but is of a continuous nature.     

Behavioral estimates of interhemispheric transmission time and the signal detection method: A reappraisal

On the basis of a review of the literature, Bashore (1981) concluded that only simple reaction time experiments with manual responses yielded consistent behavioral estimates of interhemispheric transmission time. A closer look at the data, however, revealed that these experiments were the only ones in which large numbers of observations were invariably obtained from many subjects. To investigate whether the methodological flaw was the origin of Bashore’s conclusion, two experiments were run in which subjects had to react to lateralized light flashes. The first experiment dealt with manual reactions, the second with verbal reactions. Each experiment included a condition without catch trials (i.e., simple reaction time) and two conditions with catch trials. Catch trials were trials in which no stimulus was given and in which the response was to be withheld. Both experiments returned consistent estimates of interhemispheric transmission time in the range of 2–3 msec. No differences were found between the simple reaction time condition and the signal detection conditions with catch trials. Data were analyzed according to the variable criterion theory. This showed that the effect of catch trials, as well as the effect of interhemispheric transmission, was situated at the height of the detection criterion, and not in the rate of the information transmission.     

Target-size influences on reaction time with movement time controlled

The variable that affect motor programming time may be studied by changing the nature of the response and measuring the subsequent changes in reaction time (RT). One notion of motor programming suggests that aiming responses with reduced target size and/or increased target amplitude require more "complex" motor programs that require longer RTs. In a series of five experiments which movement time (MT) was experimentally varied target size neither influences RT when the movement amplitude was 2 or 30 cm nor when the target sizes differed by as much as a factor of 16:1. Increasing the movement amplitude from 15 to 30 cm also had no influence on RT. Movement time, however, did affect RT, with 200-msec movements having longer RTs than 120-msec movements. Target size and movement amplitude did not appear to be factors that influence programming time or program complexity.     

Response facilitation and inhibition in manual, vocal, and oculomotor performance: evidence for a modality-unspecific mechanism

In 2 experiments (N = 10, Experiment 1; N = 16, Experiment 2), the authors investigated whether evidence for response facilitation and subsequent inhibition elicited by masked prime stimuli can be observed for output modalities other than manual responding. Masked primes were followed by target stimuli that required a 2-choice manual, saccadic, or vocal response. Performance was measured for compatible trials in which primes and targets were identical and for incompatible trials in which they were mapped to opposite responses. When primes were presented centrally, performance benefits were obtained for incompatible trials; whereas for peripherally presented primes, performance benefits were found in compatible trials. That pattern of results was obtained for manual responses and for saccadic eye movements (Experiment 1), demonstrating that those effects are not mediated by specialized dorsal pathways involved in visuomanual control. An analogous pattern of effects was found when manual and vocal responses were compared (Experiment 2). Because vocal responding is controlled by the inferotemporal cortex, that result shows that prime-target compatibility effects are not primarily mediated by the dorsal stream, but appear to reflect modality-unspecific visuomotor links that allow rapid activation of motor responses that may later be subject to inhibition.     

Goal-driven modulation as a function of time in saccadic target selection

Four experiments were performed to investigate the contribution of goal-driven modulation in saccadic target selection as a function of time. Observers were required to make an eye movement to a prespecified target that was concurrently presented with multiple nontargets and possibly one distractor. Target and distractor were defined in different dimensions (orientation dimension and colour dimension in Experiment 1), or were both defined in the same dimension (i.e., both defined in the orientation dimension in Experiment 2, or both defined in the colour dimension in Experiments 3 and 4). The identities of target and distractor were switched over conditions. Speed-accuracy functions were computed to examine the full time course of selection in each condition. There were three major results. First, the ability to exert goal-driven control increased as a function of response latency. Second, this ability depended on the specific target-distractor combination, yet was not a function of whether target and distractor were defined within or across dimensions. Third, goal-driven control was available earlier when target and distractor were dissimilar than when they were similar. It was concluded that the influence of goal-driven control in visual selection is not all or none, but is of a continuous nature.     

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.     

Blocking Perturbations and Multilimb Control in Rapid-Aiming Movements

The effect of an unexpected mechanical block on the control of multilimbaiming movements was studied in two experiments. In the first experiment, subjects (N = 10) attempted to push two hand levers 9 cm forward in 200 ms without vision. In the second experiment, subjects (N = 9) attempted to push hand levers and foot pedals forward 9 cm in 200 ms. After a practice period, five attempts at blocking the limb movements were made on the left lever and the right lever (Experiment 1) and on both levers (Experiment 2 only) during randomly selected trials. When one hand was blocked in Experiment 1, the other hand undershot the target on the first blocked trial, with slight reductions in movement time. When one hand was blocked in Experiment 2, the contralateral limb undershot the target on all blocked trials, but this had little effect on the lower limbs. The lower limbs undershot the target when both up- per limbs were blocked. Discrete movement corrections were made on more of the blocked trials relative to the unblocked control trials. Interlimb correlations decreased following the block, suggesting that subjects dissociated the limbs in an effort to minimize the effect of the block.     

无意识信息的刺激表征及其时间特性

无意识信息是否存在刺激表征有待解决。实验采用字母Flanker任务, 通过目标和flanker在刺激水平和反应水平上的冲突效应, 重点考察阈下flanker在刺激水平的表征。在相同的实验设计下, flanker可觉察时(实验1A), 观察到经典的刺激冲突效应和反应冲突效应; 而flanker无意识时(实验1B), 重复了反应冲突效应, 却观察到刺激冲突效应发生反转, 提示了无意识信息的反应加工及刺激加工。实验2采用符号材料促使刺激−反应的自动联结, 减少刺激−反应规则的难度, 结果重复了实验1B的发现--无意识信息引起反转的刺激冲突。刺激冲突下反转效应的一致结果表明无意识信息的刺激表征影响了认知加工。实验3考察这种影响在时间进程上的特点。无意识刺激表征的影响随反应时变化：在快速反应中观察到刺激冲突效应, 之后该效应发生反转且反转量随反应时增加而增大。相反, 无意识反应表征的影响在不同反应时下保持稳定。以上结果提供了无意识信息存在刺激表征的行为学证据并揭示了其时间特性, 提供了无意识领域中不一致研究结果的整合思路。     

Response Facilitation and Inhibition in Manual,Vocal, and Oculomotor Performance: Evidence for a Modality-Unspecific Mechanism

In 2 experiments (N = 10, Experiment 1; N = 16, Experiment 2), the authors investigated whether evidence for response facilitation and subsequent inhibition elicited by masked prime stimuli can be observed for output modalities other than manual responding. Masked primes were followed by target stimuli that required a 2-choice manual, saccadic, or vocal response. Performance was measured for compatible trials in which primes and targets were identical and for incompatible trials in which they were mapped to opposite responses. When primes were presented centrally, performance benefits were obtained for incompatible trials; whereas for peripherally presented primes, performance benefits were found in compatible trials. That pattern of results was obtained for manual responses and for saccadic eye movements (Experiment 1), demonstrating that those effects are not mediated by specialized dorsal pathways involved in visuomanual control. An analogous pattern of effects was found when manual and vocal responses were compared (Experiment 2). Because vocal responding is controlled by the inferotemporal cortex, that result shows that prime-target compatibility effects are not primarily mediated by the dorsal stream, but appear to reflect modality-unspecific visuomotor links that allow rapid activation of motor responses that may later be subject to inhibition.     

Impact forces cannot explain the one-target advantage in rapid aimed hand movements

A pointing movement is executed faster when a subject is allowed to stop at the first target than when the subject has to proceed to a second target ("one-target advantage"). Our hypothesis was that this is because the impact at the target helps to stop the finger when the finger does not have to proceed to a second target. This hypothesis would predict that the horizontal force at contact with the first target should be larger when there is only one-target. Modelling smooth movements with larger forces at contact using a minimum-jerk model, shows that the peak velocity is slightly higher and it occurs later during the movement when there is only one target. Although the one-target advantage was present in our experiment, the horizontal force at contact in the one-target condition was not larger than in the two-target condition. The time of the maximum velocity did not differ, but the maximum velocity was higher in the one-target condition. Thus our hypothesis is rejected, favouring a non-mechanical explanation of the one-target advantage.     

Brief bimanual force pulses: correlations between the hands in force and time.

Three experiments assessed coupling phenomena in the coordination of bimanual force pulses. Experiment 1 required symmetric force pulses (equal target forces and rise times for both hands) using the index finger of each hand. As the authors expected, on the basis of bimanual pointing movement results, this experiment revealed positive correlations between both the force rise times and the force amplitudes of the two hands. Experiments 2 and 3 included asymmetric conditions with different target force amplitudes (Experiment 2) or target rise times (Experiment 3). In Experiment 2 force amplitudes but not rise times were fully decoupled in the asymmetric condition. In the asymmetric condition of Experiment 3, however, neither rise times nor force amplitudes were fully decoupled. The results suggest a hierarchical control structure with temporal control dominating nontemporal control of bimanual force coordination.