Benefits and costs of self-paced preparation of novel task instructions

Errors from a serial response task involving single-finger responses to alphabetic stimuli are analysed and discussed in relation to findings which have been reported from tasks with more compatible stimulus-response relationships. Errors are divided into three distinguishable subsets and in each case found to have longer latencies than correct responses. Those which result from mirroring the required response about the centre of the hand are found to resist elimination during practice and their frequency seems to depend on the type of code used. In all cases error correction times are faster than the times to make a correct response but mirror errors and errors involving a finger adjacent to the correct response are corrected faster than other errors. The findings are discussed in relation to the theory of choice reaction time and error correction.

Primate behavior is flexible: The response to a stimulus often depends on the task in which it occurs. Here we study how single neurons in the posterior parietal cortex (PPC) respond to stimuli which are associated with different responses in different tasks. Two rhesus monkeys performed a task-switching paradigm. Each trial started with a task cue instructing which of two tasks to perform, followed by a stimulus requiring a left or right button press. For half the stimuli, the associated responses were different in the two tasks, meaning that the task context was necessary to disambiguate the incongruent stimuli. The other half of stimuli required the same response irrespective of task context (congruent). Using this paradigm, we previously showed that behavioral responses to incongruent stimuli are significantly slower than to congruent stimuli. We now demonstrate a neural correlate in the PPC of the additional processing time required for incongruent stimuli. Furthermore, we previously found that 29% of parietal neurons encode the task being performed (task-selective cells). We now report differences in neuronal timing related to congruency in task-selective versus task nonselective cells. These differences in timing suggest that the activity in task nonselective cells reflects a motor command, whereas activity in task-selective cells reflects a decision process.

Nonstutterers’, mild stutterers’, and severe stutterers’ acoustic laryngeal reaction times (LRTs) were recorded for isolated vowels and nonpropositional VCV responses in different stimulus conditions governing response preparation. In all stimulus-response conditions severe stutterers produced the longest LRTs, followed in turn by mild stutterers and nonstutterers. The three groups significantly differed from one another in most conditions, but the magnitude of difference between mild and severe stutterers was notably greater than the difference between mild stutterers and nonstutterers. LRT changes as a function of stimulus condition showed that, in general, nonstutterers were best able to use a preparation-facilitating stimulus condition to reduce LRT, and severe stutterers least able to do so. LRT changes as a function of response complexity showed that only nonstutterers produced statistically significant within-group differences. Patterns of LRT change as a combined function of group, stimulus condition, and response type suggest a complex relationship between stutterer severity, preparation time, and type of response complexity. Results illustrate aspects of Goldberg’s (1985) model of preparation processes, and support hypotheses that stutterer subgroups show differential preparation deficits along with high motor initiation variability.

The claim that event-related potentials (ERPs) index familiarity was assessed by acquiring ERPs during a recognition memory task in which participants were instructed to adopt different decision criteria in separate retrieval phases. In one, the instructions were to respond “old” only when confident that this was the correct response, and to respond “new” otherwise (the conservative condition). In the other, the instructions were to respond new only when confident that this was the correct response (the liberal condition). The rationale for this approach was that the level of familiarity licensing an old response would be higher in the conservative than in the liberal condition, and if ERPs index familiarity, this would be reflected in changes to the putative ERP index. This index comprises relatively more positive-going neural activity for correct judgments to old than to new items, which is evident from 300 to 500 msec poststimulus at mid-frontal scalp locations. In keeping with task instructions, participants made more old responses in the liberal than in the conservative condition. There were reliable mid-frontal ERP old/new effects in both conditions, and the ERPs evoked by correct judgments to words in the conservative condition were relatively more positive-going than those in the liberal condition. This finding is consistent with the view that the mid-frontal ERP old/new effect indexes familiarity, and in combination with other ERP findings, provides strong support for dual-process accounts of recognition memory.

Rule-based performance improves remarkably throughout childhood. The present study examined how children and adolescents structured tasks and implemented rules when novel task instructions were presented in a child-friendly version of a novel instruction-learning paradigm. Each miniblock started with the presentation of new stimulus-response mappings for a go task. Before this mapping could be implemented, subjects had to make responses in order to advance through screens during a preparatory (“ next”) phase. Children (4–11 years old) and late adolescents (17–19 years old) responded more slowly during the next phase when the next response was incompatible with the instructed stimulus-response mapping. This instruction-based interference effect was more pronounced in young children than in older children. We argue that these findings are most consistent with age-related differences in rule structuring. We discuss the implications of our findings for theories of rule-based performance, instruction-based learning, and development.

In a “consistent” spatial choice reaction task the same spatial relationship obtains between each stimulus and its correct response. In an “inconsistent” task this is not so. While Duncan (1977a) found both easy (spatially corresponding) and difficult (spatially opposite) responses to be slowed in inconsistent tasks, Smith (1977) found this only for the corresponding responses, the reverse holding for opposites. Reasons for this discrepancy are examined. The result of Smith (1977) depends on the use of different numbers of alternative responses in consistent and inconsistent tasks, a situation allowing no useful comparison between the two. Effects of consistency are related to others in the literature. The general conclusion is that, in these tasks, response selection is based not on a list of associations between individual stimuli and responses, but on operations or rules each of which will generate a set of stimulus–response pairs.

Abstract. Novel stimulus-response associations are retrieved automatically even without prior practice. Is this true for novel cue-task associations? The experiment involved miniblocks comprising three phases and task switching. In the INSTRUCTION phase, two new stimuli (or familiar cues) were arbitrarily assigned as cues for up-down/right-left tasks performed on placeholder locations. In the UNIVALENT phase, there was no task cue since placeholder’s location afforded one task but the placeholders were the stimuli that we assigned as task cues for the following BIVALENT phase (involving target locations affording both tasks). Thus, participants held the novel cue-task associations in memory while executing the UNIVALENT phase. Results show poorer performance in the first univalent trial when the placeholder was associated with the opposite task (incompatible) than when it was compatible, an effect that was numerically larger with newly instructed cues than with familiar cues. These results indicate automatic retrieval of newly instructed cue-task associations.

Complex behavior often requires the formation of associations between environmental stimuli and motor responses appropriate to those stimuli. Moreover, the appropriate response to a given stimulus may vary depending on environmental context. Stimulus-response associations that are adaptive in one situation may not be in another. The prefrontal cortex (PFC) has been shown to be critical for stimulus-response mapping and the implementation of task context. To investigate the neural representation of sensory-motor associations and task context in the PFC, we recorded the activity of prefrontal neurons in two monkeys while they performed two tasks. The first task was a delayed-match-to-sample task in which monkeys were presented with a sample picture and rewarded for making a saccade to the test picture that matched the sample picture following a delay period. The second task was a conditional visuomotor task in which identical sample pictures were presented. In this task, animals were rewarded for performing either prosaccades or antisaccades following the delay period depending on sample picture identity. PFC neurons showed task selectivity, object selectivity, and combinations of task and object selectivity. These modulations of activity took the form of a reduction in stimulus and delay-related activity, and a pro/anti instruction-based grouping of delay activity in the conditional visuomotor task. These data show that activity in PFC neurons is modulated by experimental context, and that this activity represents the formal demands of the task currently being performed.

Recently, a lot of research has focused on resolving whether two-digit numbers are processed holistically or compositionally. This has led to inconsistent results. In the present study we investigated effects of task instructions. Subjects performed magnitude or parity judgments on targets preceded by masked primes containing parts of the target at a task-congruent (3#_37) or task-incongruent (#3_37) position. Priming effects were influenced by the instructions: In the magnitude task, the priming effects were primarily mediated by the congruency of the decade digit, whereas in the parity task they were elicited by the congruency of the unit digit, which is in line with a flexible compositional processing style. These and previous findings show that two-digit numbers can be processed in a very flexible way, depending on the task context.

ABSTRACTThe computations underlying cognitive strategies in sensorimotor learning are poorly understood. Here we investigate such strategies in a sensorimotor transformation task. We show that strategies assume two forms, reflecting distinct working memory representations: discrete response caching of stimulus-response contingencies (e.g., look-up table; RC), and time-consuming parametric computations (e.g. mental rotation; MR). Subjects’ reaction times and errors suggest that both strategies are employed during learning, and trade off based on the progress of learning and the complexity of the task. Experiments using pressured preparation time support these working memory mechanisms: In discrete RC, time pressure elicits bimodal distributions of movements, in agreement with cached responses; in parametric MR, time pressure elicits a shifting distribution producing intermediate movements between visual targets and distal goals, consistent with analog re-computing of a movement plan. These results provide a specific model of working memory contributions to motor learning.