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.     

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.     

Facilitatory and inhibitory effects of masked prime stimuli on motor activation and behavioural performance.

Three experiments investigated the impact of information provided by masked stimuli on motor activation. Masked primes were presented prior to target stimuli and these primes were identical to the target on compatible trials, identical to the target mapped to the opposite response on incompatible trials and task-irrelevant on neutral trials. A previous study [Eimer, M., & Schlaghecken, F. (1998). Effects of masked stimuli on motor activation: Behavioural and electrophysiological evidence. Journal of Experimental Psychology: Human Perception and Performance, 24, 1737-1747] found performance costs for compatible trials and benefits for incompatible trials. Experiment 1 showed that these effects are not due to 'perceptual repetition blindness'. Experiments 2 and 3 obtained evidence for an initial response facilitation triggered by the primes that was followed by inhibition. With short intervals between prime presentation and response execution, performance benefits were found for compatible trials and these turned into costs at longer intervals. It is argued that an early response facilitation mediated by direct perceptuo-motor links is subsequently inhibited by a central mechanism operating to prevent behaviour from being controlled by irrelevant information.     

Mixing compatible and incompatible mappings: Elimination, reduction, and enhancement of spatial compatibility effects

In two-choice tasks, the compatible mapping of left stimulus to left response and right stimulus to right response typically yields better performance than does the incompatible mapping. Nonetheless, when compatible and incompatible mappings are mixed within a block of trials, the spatial compatibility effect is eliminated. Two experiments evaluated whether the elimination of compatibility effects by mixing compatible and incompatible mappings is a general or specific phenomenon. Left-right physical locations, arrow directions, and location words were mapped to keypress responses in Experiment 1 and vocal responses in Experiment 2. With keypresses, mixing compatible and incompatible mappings eliminated the compatibility effect for physical locations and arrow directions, but enhanced it for words. With vocal responses, mixing significantly reduced the compatibility effect only for words. Overall, the mixing effects suggest that elimination or reduction of compatibility effects occurs primarily when the stimulus-response sets have both conceptual and perceptual similarity. This elimination may be due to suppression of a direct response-selection route, but to account for the full pattern of mixing effects it is also necessary to consider changes in an indirect response-selection route and the temporal activation properties of different stimulus-response sets.     

Stimulus-response incompatibility eliminates inhibitory cueing effects with saccadic but not manual responses

There are thought to be two forms of inhibition of return (IOR) depending on whether the oculomotor system is activated or suppressed. When saccades are allowed, output-based IOR is generated, whereas input-based IOR arises when saccades are prohibited. In a series of 4 experiments, we mixed or blocked compatible and incompatible trials with saccadic or manual responses to investigate whether cueing effects would follow the same pattern as those observed with more traditional peripheral onsets and central arrows. In all experiments, an uninformative cue was displayed, followed by a cue-back stimulus that was either red or green, indicating whether a compatible or incompatible response was required. The results showed that IOR was indeed observed for compatible responses in all tasks, whereas IOR was eliminated for incompatible trials—but only with saccadic responses. These findings indicate that the dissociation between input- and output-based forms of IOR depends on more than just oculomotor activation, providing further support for the existence of an inhibitory cueing effect that is distinct to the manual response modality.     

Mixing location-irrelevant and location-relevant trials: influence of stimulus mode on spatial compatibility effects

The performance advantage for spatially compatible mappings of physical locations to keypress responses, relative to incompatible mappings, is eliminated when stimulus color, rather than location, is relevant on half of the trials. In Experiment 1, we compared the effects of mixing for different stimulus modes (physical locations, arrow directions, and location words) to determine whether this elimination of the stimulus-response compatibility (SRC) effect would generalize to other stimulus modes. The SRC effect was unaffected when the location information was conveyed by arrows and was amplified when the location information was conveyed by words. In Experiment 2, we used vocal left-right responses instead of keypresses, and the SRC effects for all three stimulus modes were enhanced by mixing. In both experiments, for all stimulus modes, mixing reduced or reversed correspondence effects for trials on which the location information was irrelevant when the mapping for those trials on which it was relevant was incompatible. These findings suggest that when trial types are mixed, direct activation of the corresponding response, regardless of mapping, does not occur for physical locations mapped to keypresses. However, such activation does occur when stimuli or responses are verbal, apparently because performance is mediated in part by activation of a verbal name code for the stimulus.     

Dissociating local and global levels of perceptuo-motor control in masked priming

Masked prime stimuli presented near the threshold of conscious awareness affect responses to subsequent targets. The direction of these priming effects depends on the interval between masked prime and target. With short intervals, benefits for compatible trials (primes and targets mapped to the same response) and costs for incompatible trials are observed. This pattern reverses with longer intervals. We argue (a) that these effects reflect the initial activation and subsequent self-inhibition of the primed response, and the corresponding inhibition and subsequent disinhibition of the nonprimed response, and (b) that they are generated at dissociable local (within response channels) and global (between channels) levels of motor control. In two experiments, global-level priming effects were modulated by changing the number of response alternatives, whereas local-level effects remained unaffected. These experiments suggest that low-level motor control mechanisms can be successfully decomposed into separable subcomponents, operating at different levels within the motor system.     

Response priming with apparent motion primes

Response priming refers to the finding that a prime stimulus preceding a target stimulus influences the response to the following target stimulus. Typically, responses are faster and more accurate if the prime calls for the same response as the target (i.e., compatible trials), as compared with the situation where primes and targets trigger different responses (i.e., incompatible trials). However, the effect depends on presentational and temporal parameters such as the stimulus onset asynchrony (SOA) of prime and target, or prime duration. Until now, the special role of moving stimuli was largely ignored. In the present research, experiments were conducted using clearly visible moving dots as primes and static arrows as targets. Essentially, with short SOAs up to 200 ms, participants responded faster to compatible targets. In contrast, with SOAs above 200 ms, participants responded faster to incompatible targets. The results were compared with response priming with static primes. Here, a different pattern of results emerged, with faster responses to compatible than incompatible targets at a long SOA of 300 ms. Overall, the experiments provide evidence for the existence of an inhibitory mechanism in action control when (distracting) motion stimuli are present. Results could be explained with slight changes to different accounts of negative response priming effects, as well as theories of attention.     

A central-peripheral asymmetry in masked priming

Masked primes presented prior to a target result in behavioral benefits on incompatible trials (in which the prime and the target are mapped onto opposite responses) when they appear at fixation, but in behavioral benefits on compatible trials (in which the prime and the target are mapped onto the same response) when appearing peripherally. In Experiment 1, the time course of this central-peripheral asymmetry (CPA) was investigated. For central primes, compatible-trial benefits at short stimulus onset asynchronies (SOAs) turned into incompatible-trial benefits at longer SOAs. For peripheral primes, compatible-trial benefits at short SOAs increased in size with longer SOAs. Experiment 2 showed that these effects also occur when primes and targets are physically dissimilar, ruling out an interpretation in terms of the perceptual properties of the stimulus material. In Experiments 3 and 4, the question was investigated as to whether the CPA is related to visual-spatial attention and/or retinal eccentricity per se. The results indicate that the CPA is independent of attentional factors but strongly related to the physiological inhomogeneity of the retina. It is argued that central and peripheral primes trigger an initial motor activation, which is inhibited only if primes are presented at retinal locations of sufficiently high perceptual sensitivity. The results are discussed in terms of an activation threshold model.     

Inhibition of return in manual and saccadic response systems

When nonpredictive exogenous visual cues are used to reflexively orient covert visual spatial attention, the initial early facilitation for detecting stimuli at cued versus uncued spatial locations develops into inhibition by 300 msec following the cue, a pattern referred to as inhibition of return (IOR). Experiments were carried out comparing the magnitude and time course for development of IOR effects when manual versus saccadic responses were required. The results showed that both manual and saccadic responses result in equivalent amounts of facilitation following initial exposure to a spatial cue. However, IOR developed more quickly for saccadic responses, such that, at certain cue-target SOAs, saccadic responses to targets were inhibited, whereas manual responses were still facilitated. The findings are interpreted in terms of a premotor theory of visual attention.     

The effect of nonmasking distractors on the priming of motor responses

Masked stimuli (primes) can affect the preparation of a motor response to subsequently presented target. In numerous studies, it has been shown that the compatibility effect is biphasic as it develops over time: positive (benefits for compatible trials and costs for incompatible trials) for short prime-target temporal distances and negative (benefits for incompatible trials and costs for compatible trials) for long ones. What triggers the 2nd phase is the matter of the current debate. According to the self-inhibition hypothesis, the motor response elicited by a prime is automatically followed by an inhibition phase. The object-updating and mask-triggered inhibition hypotheses assume that this phase is triggered by the mask, provided that it contains features calling for the alternative response. In the present study, the author shows that the compatibility effect is modulated on the temporal position of a nonmasking distractor presented after the prime and before the target. With a distractor possessing task-relevant features, the compatibility effect was found to be negative for short prime- distractor intervals and for moderate prime-target intervals. The consequences of these results for the 3 hypotheses are discussed.     

The role of emotional context in facilitating imitative actions

In two experiments, we explored whether emotional context influences imitative action tendencies. To this end, we examined how emotional pictures, presented as primes, affect imitative tendencies using a compatibility paradigm. In Experiment 1, when seen index finger movements (lifting or tapping) and pre-instructed finger movements (tapping) were the same (tapping–tapping, compatible trials), participants were faster than when they were different (lifting–tapping, incompatible trials). This compatibility effect was enhanced when the seen finger movement was preceded by negative primes compared with positive or neutral primes. In Experiment 2, using only negative and neutral primes, the influence of negative primes on the compatibility effect was replicated with participants performing two types of pre-instructed finger movements (tapping and lifting). This emotional modulation of the compatibility effect was independent of the participants' trait anxiety level. Moreover, the emotional modulation pertained primarily to the compatible conditions, suggesting facilitated imitation due to negatively valent primes rather than increased interference. We speculate that negative stimuli increase imitative tendencies as a natural response in potential flight-or-fight situations.     

Partial response activation to masked primes is not dependent on response readiness

Masked primes presented foveally prior to a target trigger an initial partial activation of their corresponding response, followed by an inhibition of the same response. The latter phase results in performance costs on compatible trials and performance benefits on incompatible trials relative to neutral trials (negative compatibility effect). The present study investigated whether this activation-follow-by-inhibition process depends on the overall or specific state of response readiness. In two masked priming experiments, response readiness was manipulated by varying the relative frequency of Go-trials in a Go/NoGo task (Exp. 1) and the relative frequency of left- and right-hand responses in a 2-alternative choice reaction time task (Exp. 2). In both experiments, mean reaction times were longer for infrequent responses than for frequent responses. However, negative compatibility effects were not affected by response frequency. This result indicates that neither the general ability of masked primes to elicit a partial motor activation nor the specific time course of this process is dependent on response readiness. It is concluded that response readiness affects the execution of an overt response rather than the initial activation of this response.     

Coactivation in the perception of redundant targets

Reaction time (RT) to redundant stimuli was investigated while controlling for distraction effects and response competition. In Experiment 1, a redundancy gain was found for 2 target letters with identical features (redundant) compared to trials in which 2 different targets shared the same response assignment (compatible) indicating coactivation of stimulus inputs. No difference in RTs was found between compatible displays and displays containing 2 targets with different responses (incompatible), suggesting (with other evidence) that letters were serially processed. In Experiment 2, a redundancy gain was again found. Unlike in Experiment 1, incompatible displays produced response competition, indicating a redundancy gain with parallel processing. Three forms of redundancy gains operating under specific conditions are discussed.     

Between-task transfer of learning from spatial compatibility to a color stroop task

Responses to a relevant stimulus dimension are faster and more accurate when the stimulus and response spatially correspond compared to when they do not, even though stimulus position is irrelevant (Simon effect). It has been demonstrated that practicing with an incompatible spatial stimulus-response (S-R) mapping before performing a Simon task can eliminate this effect. In the present study we assessed whether a learned spatially incompatible S-R mapping can be transferred to a nonspatial conflict task, hence supporting the view that transfer effects are due to acquisition of a general "respond to the opposite stimulus value" rule. To this aim, we ran two experiments in which participants performed a spatial compatibility task with either a compatible or an incompatible mapping and then transferred, after a 5 min delay, to a color Stroop task. In Experiment 1, responses were executed by pressing one of two keys on the keyboard in both practice and transfer tasks. In Experiment 2, responses were manual in the practice task and vocal in the transfer task. The spatially incompatible practice significantly reduced the color Stroop effect only when responses were manual in both tasks. These results suggest that during practice participants develop a response-selection strategy of emitting the alternative spatial response.     

Response inhibition under task switching: its strength depends on the amount of task-irrelevant response activation

Under task switch conditions, response repetitions usually produce benefits if the task also repeats, but costs if the task switches. So far, it is largely undecided how to account for these effects. In the present study, we provide additional evidence in favor of the account that each response is inhibited in order to prevent its accidental re-execution. To test this hypothesis, the risk of an accidental re-execution of a given response was manipulated by modulating the activation of the response in the previous task. In Experiment 1, this was done by means of congruent and incongruent stimuli. As expected, on task switch trials, the repetition costs were larger if a congruent rather than an incongruent stimulus occurred in the previous task. In Experiment 2, the same effect occurred for stimulus-response compatible versus incompatible stimuli in the previous task. In Experiment 3, both manipulations were applied together, which produced almost additive effects. Altogether, the results support the inhibition account for the response repetition effects under task switch conditions.     

Coloring only a single letter does not eliminate color-word interference in a vocal-response Stroop task: automaticity revealed

The presence of an interference effect in naming the print color of color words (J. R. Stroop, 1935) suggests that responses associated with the irrelevant-word dimension of the display are activated involuntarily. In the present study, the author examined the conditions under which coloring a single letter in a word reduced interference in vocal responding (D. Kahneman & A. Henik, 1981) or eliminated it in manual responding (D. Besner, J. A. Stolz, & C. Boutilier, 1997). In Experiment 1, color-word interference was significant under vocal responding for the Besner et al. displays. In Experiment 2, the author replicated the Kahneman and Henik effect with the Besner et al. stimuli. The results of Experiment 3 showed that semantic effects are not eliminated by coloring only a single letter. Coloring a single letter does not prevent the activation of the irrelevant-word dimension of the colored color word.     

Coloring Only a Single Letter Does Not Eliminate Color-Word Interference in a Vocal-Response Stroop Task: Automaticity Revealed

The presence of an interference effect in naming the print color of color words (J. R. Stroop, 1935) suggests that responses associated with the irrelevant-word dimension of the display are activated involuntarily. In the present study, the author examined the conditions under which coloring a single letter in a word reduced interference in vocal responding (D. Kahneman & A. Henik, 1981) or eliminated it in manual responding (D. Besner, J. A. Stolz, & C. Boutilier, 1997). In Experiment 1, color-word interference was significant under vocal responding for the Besner et al. displays. In Experiment 2, the author replicated the Kahneman and Henik effect with the Besner et al. stimuli. The results of Experiment 3 showed that semantic effects are not eliminated by coloring only a single letter. Coloring a single letter does not prevent the activation of the irrelevant-word dimension of the colored color word.     

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.     

The sensorimotor contributions to implicit memory, familiarity, and recollection

The sensorimotor contributions to memory for prior occurrence were investigated. Previous research has shown that both implicit memory and familiarity draw on gains in stimulus-related processing fluency for old, compared with novel, stimuli, but recollection does not. Recently, it has been demonstrated that processing fluency itself resides in stimulus-specific motor simulations or reenactment (e.g., covert pronouncing simulations for words as stimuli). Combining these lines of evidence, it was predicted that stimulus-specific motor interference preventing simulations should impair both implicit memory and familiarity but leave recollection unaffected. This was tested for words as verbal stimuli associated to pronouncing simulations in the oral muscle system (but also for tunes as vocal stimuli and their associated vocal system, Experiment 2). It was found that oral (e.g., chewing gum), compared with manual (kneading a ball), motor interference prevented mere exposure effects (Experiments 1-2), substantially reduced repetition priming in word fragment completion (Experiment 3), reduced the familiarity estimates in a remember-know task (Experiment 5) and in receiver-operating characteristics (Experiment 6), and completely neutralized familiarity measured by self-reports (Experiment 4) and skin conductance responses (Experiment 7), while leaving recollection and free recall unaffected (across Experiments 1-7). This pattern establishes a rare memory dissociation in healthy participants, that is, explicit without implicit memory or recognizing without feeling familiar. Implications for embodied memory and neuropsychology are discussed.