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

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

任务切换理论争议新证据

任务切换是研究认知控制的主要范式之一。大量研究发现切换试次比重复试次的反应时更长,错误率更高,这种差异称为切换代价。任务切换时所产生切换代价的理论解释主要有惯性论、重构论和联结论。近十年来,这些理论均获得新的实验支持和发展,但其争议依旧,没有哪一理论能成功解释任务切换的所有效应。未来研究可以建立整合模型,以准确描述切换代价产生的认知机制。     

Clever homunculus: is there an endogenous act of control in the explicit task-cuing procedure?

Does the explicit task-cuing procedure require an endogenous a act of control? In 5 experiments, cues indicating which task to perform preceded targets by several stimulus onset asynchronies (SOAs). Two models were developed to account for changes in reaction time (RT) with SOA. Model 1 assumed an endogenous act of task switching for cue alterations but not for cue repetitions. Model 2 assumed no such act. In Experiments 1 and 2, the cue was masked or not masked. Masking interacted underadditively with repetition and alternation, consistent with Model 2 but not Model 1. In Experiments 3 and 4, 2 cues were used for each task. RT was slower for task repetition than for cue repetition and about the same as RT for task alternation, consistent with Model 2 but not Model 1. The results suggest that the explicit task-cuing procedure does not require an endogenous act of control.     

Modality-specific preparatory influences on the flexibility of cognitive control in task switching

In the current study, we addressed modality-specificity of the flexibility of cognitive control. We compared performance in single-task and mixed-tasks blocks between blocked auditory and visual stimuli assessing alternation costs (single vs. mixed). Mixed blocks comprised task switches only. The tasks consisted of numerical parity, magnitude, and distance judgments about numbers between one and nine without five. A cue indicated the relevant task. The cue–stimulus interval was varied (short vs. long interval) to examine preparation effects. The results indicated higher response times (RTs) and error rates (ERs) in mixed- vs. single-tasks blocks. The alternation costs in ERs were larger for auditory compared to visual stimulus presentation. Moreover, the reduction of RT alternation costs based on increased preparation time was more pronounced for the auditory modality compared to the visual modality. These results suggest a modality-specific influence on processes involved in maintaining and updating task sets in working memory.     

Signal recognition as influenced by presentation schedules

Performance in a recognition task involving two amplitudes of the same tone was investigaled over a wide range of presentation schedules. The task was arranged so that there was no trial-to-trial feedback or other information regarding the relative frequencies of the two tones. The hit and false alarm rates (the proportion of “loud” responses to loud and soft stimuli, respectively) on any given trial were strongly influenced by the stimulus and response on the preceding trial. In general, Ss tended to repeat the last response and were more accurate after a stimulus alternation than after a stimulus repetition. In addition, hit and false alarm rates were inversely related to the presentation probability of the loud tone, in contrast to the direct relation typically found in signal detection experiments and in recognition experiments with trial-to-trial feedback. A mathematical model incorporating three processes (memory, comparison, and decision) was shown to give a good account of these data.     

The role of sensory-motor modality compatibility in language processing

Language processing requires the combination of compatible (auditory-vocal and visual-manual) or incompatible (auditory-manual and visual-vocal) sensory-motor modalities, and switching between these sensory-motor modality combinations is very common in every-day life. Sensory-motor modality compatibility is defined as the similarity of stimulus modality and the modality of response-related sensory consequences. We investigated the influence of sensory-motor modality compatibility during performing language-related cognitive operations on different linguistic levels. More specifically, we used a variant of the task-switching paradigm, in which participants had to switch between compatible or between incompatible sensory-motor modality combinations during a verbal semantic categorization (Experiment 1) or during a word-form decision (Experiment 2). The data show higher switch costs (i.e., higher reaction times and error rates in switch trials compared to repetition trials) in incompatible sensory-motor modality combinations than in compatible sensory-motor modality combinations. This was true for every language-related cognitive operation, regardless of the individual linguistic level. Taken together, the present study demonstrates that sensory-motor modality compatibility plays an important role in modality switching during language processing.     

Conflicting visual and tactual-kinesthetic stimulation

The effects of stimulus and response probability on choice reaction time (RT) were independently investigated. In different conditions, two sets of three stimuli of probabilities of.1, .3, .6 and.3, .3, .4 were assigned to two responses-two of the stimuli assigned to one response. All combinations of S-R assignments were studied, yielding response probabilities of .1-.9, ,3-.7, and ,4-.6. With response probability held constant, variations in stimulus probability led to consistent and substantial effects on both RT and error rates. Response-probability effects were confined to error rates, and repetition effects were negligible. The results support the assumption of recent models of choice behavior that adjustments are made to the absolute (rather than just to the ordinal) values of stimulus probability.     

Stimulus–classification and stimulus–action associations: Effects of repetition learning and durability

It has been shown that acquired stimulus–response bindings result from at least two types of associations from the stimulus to the task (stimulus–task or stimulus–classification; S–C) and from the stimulus to the motor response (stimulus–response or stimulus–action; S–A). These types of associations have been shown to independently affect behaviour. This finding suggests that they are processed in different pathways or different parts of a pathway at the neural level. Here we test a hypothesis that such associations may be differentially affected by repetition learning and that such effects may be detected by measuring their durability against overwriting. We show that both S–C and S–A associations are in fact strengthened when learning is boosted by increasing repetitions of the primes. However, the results further suggest that associations between stimuli and actions have less durable effects on behaviour and that the durability of S–C and S–A associations is independent of repetition learning. This is an important finding for the understanding of the underlying mechanisms of associative learning and particularly raises the question of which processes may affect flexibility of learning.     

Saccade landing point selection and the competition account of pro- and antisaccade generation: the involvement of visual attention--a review

This paper presents a review and summary of experimental findings on the role of attention in the preparation of saccadic eye movements. The focus is on experiments where performance of prosaccades (saccades towards a suddenly appearing item) and antisaccades (saccades of equal amplitude in the direction opposite to where the target moved) is compared. Evidence suggests that these two opposite responses to the same stimulus event entail competition between neural pathways that generate reflexive movements to the target and neural mechanisms involved in inhibiting the reflex and generating a voluntary gaze shift in the opposite direction to the target appearance. Evidence for such a competition account is discussed in light of a large amount of experimental findings and the overall picture clearly indicates that this competition account has great explanatory power when data on saccadic reaction times and error rates are compared for the two types of saccade. The role of attention is also discussed in particular in light of the finding that the withdrawal of attention by a secondary task 200 to 500 ms before the saccade target appears, leads to speeded antisaccades (without a similar increase in error rates), showing that the results do not simply reflect a speed-accuracy trade-off. This result indicates that the tendency for "reflexive" prosaccades is diminished when attention is engaged in a different task. Furthermore, experiments are discussed that show that as the tendency for a reflexive prosaccade is weakened, antisaccades are speeded up, further supporting the competition account of pro- and antisaccade generation. In the light of evidence from neurophysiology of monkeys and humans, a tentative model of pro- and antisaccade generation is proposed.     

Sequential effects on speeded information processing: a developmental study

Two experiments were performed to assess age-related changes in sequential effects on choice reaction time (RT). Sequential effects portray the influence of previous trials on the RT to the current stimulus. In Experiment 1, three age groups (7-9, 10-12, and 18-25 years) performed a spatially compatible choice task, with response-to-stimulus intervals (RSIs) of 50 and 500 ms varied between trial blocks. In Experiment 2, three age groups (7-9, 15-16, and 18-25 years) performed the task with spatial stimulus-response (S-R) mappings (compatible versus incompatible) varied between participants. For adults, the experiments yielded a pattern of sequential effects suggestive of "automatic facilitation" (i.e., a first-order repetition effect and a higher order benefit-only pattern for short RSIs) and "subjective expectancy" (i.e., a first-order alternation effect and a higher order cost-benefit pattern for long RSIs). Automatic facilitation was more pronounced for incompatible responses than for compatible responses. Both experiments showed the anticipated decrease in automatic facilitation with advancing age. Finally, the first-order alternation effect showed the predicted age-related increase, but the cost-benefit pattern revealed an opposite trend, suggesting that the first-order and higher order indexes of subjective expectancy may relate to dissociable mechanisms.     

The phonological loop in task alternation and task repetition

It has recently been proposed that task repetition is easier than task alternation because the appropriate task settings are already present in working memory, whereas during task alternation task settings must be retrieved from long-term memory (Mayr & Kliegl, 2000). The present study tested whether the phonological loop is involved in keeping the relevant task settings active in working memory. It may then be expected that concurrent articulatory suppression would diminish the facilitation associated with task repetition because the phonological loop could no longer maintain the appropriate task settings active in working memory. Both during task repetition and task alternation the relevant task settings should then be retrieved from long-term memory. Three dual-task experiments were conducted. The results of Experiment 1 were in support of our prediction. Experiment 2 replicated the findings of Experiment 1 and showed that the task settings probably represent the adequate response mappings. Experiment 3 ruled out the involvement of the visuo-spatial sketchpad and more general coordination demands during dual tasking.     

The phonological loop in task alternation and task repetition

It has recently been proposed that task repetition is easier than task alternation because the appropriate task settings are already present in working memory, whereas during task alternation task settings must be retrieved from long-term memory (Mayr & Kliegl, 2000). The present study tested whether the phonological loop is involved in keeping the relevant task settings active in working memory. It may then be expected that concurrent articulatory suppression would diminish the facilitation associated with task repetition because the phonological loop could no longer maintain the appropriate task settings active in working memory. Both during task repetition and task alternation the relevant task settings should then be retrieved from long-term memory. Three dual-task experiments were conducted. The results of Experiment 1 were in support of our prediction. Experiment 2 replicated the findings of Experiment 1 and showed that the task settings probably represent the adequate response mappings. Experiment 3 ruled out the involvement of the visuo-spatial sketchpad and more general coordination demands during dual tasking.     

Covert effects of alcohol revealed by event-related potentials

Contradictory evidence as to the effects of alcohol on early information processing stages has been obtained from behavioral and psychophysiological investigations. In the present study, choice reaction times, error rates, and event-related potentials (EEPs) were recorded in a task in which variations in stimulus discriminability and of the (task irrelevant) correspondence between stimulus location and response location were orthogonally combined. Both discriminability and stimulus-response correspondence affected reaction time and electrophysiological Chronometrie measures as expected. However, no behavioral effects of alcohol were observed, possibly because of strategic adjustments. Psychophysiological Chronometrie measures indicated that alcohol leaves the initial flow of perceptual evidence to motor stages unimpaired, whereas it appears to increase the duration of stimulus evaluation. Interestingly, a number of alcohol effects appeared in the EEP amplitudes. Decrements in early EEP components indicate alcohol-induced impairments of involuntary visual attention and/or the automatic stimulus location-dependent activation of response channels. In contrast, a strong enhancement of a late slow-wave component under alcohol may reflect the investment of processing resources in order to maintain normal performance levels.     

Feature integration is not the whole story of the sequence effects of symbolic cueing

ABSTRACT

Sequential modulations in symbolic cueing tasks have been attributed to complete versus partial repetition/alternation of stimulus features between consecutive trials. This feature-integration hypothesis is questioned by recent findings and further investigated in the present study. In the first two experiments, when the cueing axes switched between trials, only complete alternation of cue directions and target locations existed. Nevertheless, significant sequence effects were still found in this condition, which did not support the feature-integration hypothesis. Furthermore, although sequence effects were still significant when stimulus identities were manipulated in Experiment 3, it was abolished when different cue categories (gaze and arrow) were presented as cues in Experiment 4. The findings suggest that the integration of stimulus features is not the only source of the sequential effect and some higher level cognitive mechanisms, possibly as described in the task-file or task organization hypotheses, are involved in the sequential modulations of symbolic cueing.     

Bimodal and trimodal multisensory enhancement: effects of stimulus onset and intensity on reaction time

Manual reaction times to visual, auditory, and tactile stimuli presented simultaneously, or with a delay, were measured to test for multisensory interaction effects in a simple detection task with redundant signals. Responses to trimodal stimulus combinations were faster than those to bimodal combinations, which in turn were faster than reactions to unimodal stimuli. Response enhancement increased with decreasing auditory and tactile stimulus intensity and was a U-shaped function of stimulus onset asynchrony. Distribution inequality tests indicated that the multisensory interaction effects were larger than predicted by separate activation models, including the difference between bimodal and trimodal response facilitation. The results are discussed with respect to previous findings in a focused attention task and are compared with multisensory integration rules observed in bimodal and trimodal superior colliculus neurons in the cat and monkey.     

Common features of the “repetition” and “same-different” effects in reaction time experiments

Using comparable stimulus and response sets, and the same Ss, the “repetition” and “same-different” effects were studied in two experiments involving several reaction-time (RT) tasks. In Experiment 1, these effects were examined at a 2-sec interval between successive stimuli in the simple (SRT), the recognition (RRT), the choice (CRT), the same-different recognition(S-DRRT),and the same-different choice (S-DCRT) tasks. In Experiment 2, the effects were studied at a 1 O-sec interval in the CRT and S-DCRT tasks. The results suggest the following mainconclusions: (1)The positive repetition effect (i.e., shorter reaction times on “repeated” trials than on “nonrepeated” trials) is not only a feature of the CRT task but may also occur in the SRT and RRT tasks. (2) With increasing intertrial interval, the magnitude of the positive repetition effect diminishes and then reverses into a negative repetition effect. (3) The positive same-different effect (ie., shorter reaction times on “same” trials than on “different” trials) is affected by an increase in interstimulus interval ina manner that parallels the effect of intertrial interval on the positive repetition effect, suggesting that the processes underlying the two effects are mainly the same. (4) These changes in the magnitude and direction of the repetition and same-different effects are probably a function of discrimination difficulty.     

Sequential analysis of the numerical Stroop effect reveals response suppression

Automatic processing of irrelevant stimulus dimensions has been demonstrated in a variety of tasks. Previous studies have shown that conflict between relevant and irrelevant dimensions can be reduced when a feature of the irrelevant dimension is repeated. The specific level at which the automatic process is suppressed (e.g., perceptual repetition, response repetition), however, is less understood. In the current experiment we used the numerical Stroop paradigm, in which the processing of irrelevant numerical values of 2 digits interferes with the processing of their physical size, to pinpoint the precise level of the suppression. Using a sequential analysis, we dissociated perceptual repetition from response repetition of the relevant and irrelevant dimension. Our analyses of reaction times, error rates, and diffusion modeling revealed that the congruity effect is significantly reduced or even absent when the response sequence of the irrelevant dimension, rather than the numerical value or the physical size, is repeated. These results suggest that automatic activation of the irrelevant dimension is suppressed at the response level. The current results shed light on the level of interaction between numerical magnitude and physical size as well as the effect of variability of responses and stimuli on automatic processing.     

Perceptual and conceptual sources of priming on a word generation task

Repetition of any number of cognitive processes can facilitate subsequent performance (i.e., repetition priming). In this study, we explored several candidate mechanisms that could account for repetition priming on a word generation task. In Experiment 1, we examined whether repetition of semantic processing is necessary for priming on this task. In Experiment 2, we examined whether repetition of semantic processing is sufficient for priming on this task. In both experiments, we additionally examined the effect of changing the specific nature of the semantic retrieval task (i.e., from visual to functional, and vice versa) on performance. The results from these experiments indicated that repetition of semantic processing is both necessary and sufficient to produce a facilitation effect on the word generation task. However, semantic processing of the same attribute does not need to be repeated for facilitation effects to occur. Implications of these findings for theories of the representation and retrieval of semantic knowledge are discussed.     

Repetition costs in word identification: evaluating a stimulus–response integration account

Stimulus repetition facilitates performance in many experimental contexts. However, an episodic approach to interpreting repetition effects suggests that repetition effects should depend on how stimuli are encoded. In Experiments 1-3, stimulus repetition in a word identification task led to a cost rather than a benefit in performance, but only when the prime was presented for a relatively long duration. One account of these results is that long prime durations allow integration between stimulus and response codes to occur, which in turn can interfere with responding to a following identical target. In Experiment 4, a stimulus intensity based episodic specificity effect that was insensitive to the proportion of repeated trials supported this stimulus-response integration account.     

Switching of response modalities

When participants perform a sequence of different tasks, it is assumed that the engagement in one task leads to the inhibition of the previous task. This inhibition persists and impairs performance when participants switch back to this (still inhibited) task after only one intermediate trial. Previous task-switching studies on this issue have defined different tasks at the level of stimulus categorization. In our experiments we used different response modalities to define tasks. Participants always used the same stimulus categorization (e.g., categorize a digit as odd vs. even), but had to give a vocal, finger, or foot response (A, B, or C). Our results showed a higher reaction time and error rate in ABA sequences than in CBA sequences, indicating n - 2 repetition cost as a marker for persisting task inhibition. We assume that different response modalities can define a task and are inhibited in a “task switch” in the same way as stimulus categories are inhibited.